Scholarly article on topic 'A Review of Enzymatic Transesterification of Microalgal Oil-Based Biodiesel Using Supercritical Technology'

A Review of Enzymatic Transesterification of Microalgal Oil-Based Biodiesel Using Supercritical Technology Academic research paper on "Chemical engineering"

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Enzyme Research
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Academic research paper on topic "A Review of Enzymatic Transesterification of Microalgal Oil-Based Biodiesel Using Supercritical Technology"

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Volume 2011, Article ID 468292, 25 pages doi:10.4061/2011/468292

Review Article

A Review of Enzymatic Transesterification of Microalgal Oil-Based Biodiesel Using Supercritical Technology

Hanifa Taher,1 Sulaiman Al-Zuhair,1 Ali H. Al-Marzouqi,1 Yousef Haik,2 and Mohammed M. Farid3

1 Chemical and Petroleum Engineering Department, UAE University, Al-Ain 17555, United Arab Emirates

2 Mechanical Engineering Department, UAE University, Al-Ain 17555, United Arab Emirates

3 Chemical and Materials Engineering Department, University of Auckland, 1142 Auckland, New Zealand

Correspondence should be addressed to Sulaiman Al-Zuhair, Received 14 January 2011; Accepted 14 July 2011 Academic Editor: K. B. Ramachandran

Copyright © 2011 Hanifa Taher et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Biodiesel is considered a promising replacement to petroleum-derived diesel. Using oils extracted from agricultural crops competes with their use as food and cannot realistically satisfy the global demand of diesel-fuel requirements. On the other hand, microalgae, which have a much higher oil yield per hectare, compared to oil crops, appear to be a source that has the potential to completely replace fossil diesel. Microalgae oil extraction is a major step in the overall biodiesel production process. Recently, supercritical carbon dioxide (SC-CO2) has been proposed to replace conventional solvent extraction techniques because it is nontoxic, nonhazardous, chemically stable, and inexpensive. It uses environmentally acceptable solvent, which can easily be separated from the products. In addition, the use of SC-CO2 as a reaction media has also been proposed to eliminate the inhibition limitations that encounter biodiesel production reaction using immobilized enzyme as a catalyst. Furthermore, using SC-CO2 allows easy separation of the product. In this paper, conventional biodiesel production with first generation feedstock, using chemical catalysts and solvent-extraction, is compared to new technologies with an emphasis on using microalgae, immobilized lipase, and SC-CO2 as an extraction solvent and reaction media.

1. Introduction

Continuous exploration and consumption of fossil fuels have led to a decline in worldwide oil reserves. As the world energy demand is continuously increasing, the most sufficient way to meet the growing demand is by finding alternative fuels. From the point of environment protection, finding alternative fuels that are sustainable and environment friendly is essential.

More than a century ago, Rudolf Diesel tested the suitability of using vegetable oils as fuel in his engine [1,2]. In the 1930s and 1940s, vegetable oils were used as a diesel fuel for emergency situations. At that time, vegetable oil fuels were not competitive because they were more expensive than petroleum fuels, and therefore the idea was abandoned. With the worries about petroleum fuel availability and latest increases in petroleum prices, using vegetable oils in diesel engines has regained attention.

A number of studies have shown that triglycerides (TGs) hold promise as alternative diesel engine fuels [2, 3]. This has an advantage of being available, renewable with higher cetane number, and biodegradable [4-6]. However, the main disadvantage of oils is their high viscosity and low volatility [2, 7, 8]. Therefore, direct use of TGs is generally unacceptable and not practical since it causes engine coking, carbon depositing and gelling of the lubricating oil [8-10]. To overcome these problems, dilution, pyrolysis, cracking, and transesterification of the oil have been suggested [5, 11]. Among all these methods, transesterification has been used widely as a favorable method. Transesterification reaction of TGs, known as alcoholysis, is an important reaction that produces fatty acids alkyl esters (FAAE) [8, 12]. It was reported that replacing petroleum diesel with FAAE results in a reduction ofunburned hydrocarbons, carbon monoxide (CO), and particular matter (PM) formation [13, 14]. Several methods of transesterification using alkali catalysts

[9, 14-18], acid catalysts [17, 19-23], and enzyme lipase in presence and absence of solvents have been reported [24-29]. Most of the commercial biodiesel processes require the use of a catalyst, which requires a recovery unit to separate reaction products and remove the catalyst. These disadvantages of using catalyst could be eliminated by carrying out noncat-alytic reaction. Sake and Kusdiana [30] developed a method using supercritical methanol (SCM) where triglycerides fatty acids were converted to methyl esters without using any catalyst. Sake and Kusdiana [30] and Madras et al. [31] reported the advantage of using supercritical alcohols (SCA), especially methanol, whereas a process requires short reaction time and no need for reaction product separation from the solvent. However, this process is energy intensive as it is carried out at the supercritical conditions of methanol. Nevertheless, based on van Kasteren and Nisworo [32] economic assessment, this process appears to be feasible.

Enzymatic biodiesel approach showed promising results due to their high selectivity and mild operative conditions. Enzymatic transesterification reaction is similar to conventional transesterification, except that they are catalyzed by a variety of biological catalysts rather than chemical catalysts. In contrast to conventional processes, biocatalysts can transesterify TGs with a high free fatty acid (FFA) content [33]. Lipase-catalyzed transesterification of TG has been investigated by several investigators [33-37]. One common drawback with the use of enzyme-based processes is the high cost of the enzyme compared to conventional chemical catalysts; therefore, their recycle is required, which is possible through enzyme immobilization.

Immobilization of enzymes has generally been used to attain reusable enzyme with lower production cost [25, 38, 39]. Thus, immobilized form of lipase has been used in most of transesterification processes [25, 36, 40]. Besides enzyme reusability, other advantages of using immobilized lipase as a catalyst are enhanced activity and stability [41, 42].

Several researches have been carried out to produce biodiesel in solvent systems. Presently, industries are facing problems in using conventional solvents due to environmental worries. In the last couple of decades, enzyme-catalyzed reactions in supercritical carbon dioxide (SC-CO2) has been studied. Previously, most of the studies were investigating the feasibility of using biocatalyst in SC-CO2, whereas recent studies are focusing on obtaining good yield and conversions.

Vegetable oils consist of TG of straight chains of fatty acids. With the high cost of biodiesel produced from vegetable oils, researchers are looking for low-cost feedstocks. For that waste oils, cooking oils and fats from animal sources were proposed. The main drawback of using animal fats is their high melting points, which may require the use of organic solvents. However, organic solvent use requires a solvent recovery unit and energy needed for its separation. To overcome this, supercritical fluids (SCFs) were introduced.

During the past decades, SCFs have been investigated as alternative solvents for reactions rather than using conventional solvents. Among all supercritical fluids, SC-CO2 is the most appropriate choice as a consequence of its availability. In general, CO2 is nontoxic, nonflammable, environmentally

friendly, and recyclable fluid [43]. Thus, reactions in SC-CO2 media become the preferable route for chemical synthesis.

Conventionally, biodiesel is produced from vegetable oils, animal fats, and waste cooking oils [7, 30, 31, 44-46]. However, these feedstocks are inefficient and unsustainable [47]. Furthermore, using vegetable oil as a fuel source competes with its use as food and proposes for land development in order not to compete with food and land. On the other hand, animal fat cannot be considered as a continuous supply of feed stock [48]. Thus, biodiesel production using these feedstocks, realistically, cannot replace all world biodiesel requirements.

In contrast, microalgae have been recognized as a promising alternative source for biodiesel production. They are a group of organisms that can grow photosynthetically and accumulate large amounts of lipids [49, 50]. According to Sheehan et al. [50], if microalgal oil production could be scaled up, less than 6 million hectares would be required to meet current fuel demands.

Considering the above facts, this paper provides an overview on biodiesel production from microalgae with a particular emphasis on the use of microalgae as a promise feedstock, lipase as promise catalyst, and SC-CO2 as a promise extraction solvent and reaction media.

2. Biodiesel

Biodiesel has arisen as a possible alternative for petroleum diesel because of the similarities that biodiesel has with petroleum diesel [39, 51]. Biodiesel fuel has many advantages over petroleum fuel such as being nontoxic, biodegradable, renewable, and do not contribute to net accumulation of the green house gases [52, 53]. Also, biodiesel has lower sulfur and aromatic content, higher cetane number, and flash point than petroleum diesel [5, 7, 54-56]. Other benefits of biodiesel include increased lubricity and lower emissions of certain harmful exhaust gases in comparison to petroleum diesel fuel [55].

Comparing petroleum diesel fuel to biodiesel, Schumacher et al. [14] reported that biodiesel results in a 45% reduction in total hydrocarbon emissions, 47% reduction in CO emissions, and 66% reduction in PM emissions, whereas, Demirbas [55] reported a 42% reduction in CO and 55% in PM emissions relative to standard diesel fuel. These effects are generally attributed to the higher cetane number and oxygen content of biodiesel fuel. Although the biodiesel environmental considerations are very positive, biodiesel increases nitrogen oxides (NOx) emissions. However, reports show that reductions in NOx emissions are possible with some modifications in combustion temperatures and injection timing [57, 58].

As mentioned earlier, direct use of vegetable oil has several negative aspects, such as their high viscosity and low volatility, which lead to incomplete combustion in diesel engines, therefore, carbon deposition [5, 9, 59, 60]. However, the direct use of vegetable oils as biodiesel may be possible by mixing them with conventional diesel in an appropriate ratio, but this mixing will be impractical for long-term

uses in the engine due to the high viscosity, low stability, acid composition, and FFA content [4, 61, 62]. Therefore, considerable efforts have been made to develop vegetable oil derivatives that have properties near those of the petroleum-based diesel fuels.

Pyrolysis (cracking), microemulsion, and transesterifica-tion are the possible methods to minimize problems associated with feedstock use [5, 8, 11]. The first two methods are costly and yield low quality biodiesel, whereas the latter, transesterification, is the most common method to transform oil into biodiesel, which is the focus of this paper.

2.1. Transesterification. Transesterification is the common method used to transform TG into biodiesel. This consists of the reaction between TG and an acyl-acceptor [11, 63]. Carboxylic acids, alcohols, or another ester can be used as acyl-acceptor. Transesterification produces glycerol when alcohol is used as acyl-acceptor or triacylglycerol when ester is used [8, 56, 60, 62, 64]. Transesterification process using a catalyst is called catalytic transesterification process, whereas that without catalyst is called noncatalytic transesterification process [8, 10, 65, 66]. Moreover, catalytic process is divided into two types: homogenous and heterogeneous processes depending on the catalyst used.

Transesterification is a chemical process of transforming large and branched TG into smaller and straight chain molecules, which is similar in size to the molecules of the species present in diesel fuel [67, 68]. Stoichiometrically, for each mole of TG three moles of alcohol are required. But in general, a higher molar ratio of alcohol is used in order to achieve maximum biodiesel production. This molar ratio depends on the type of used feedstock, type of catalyst, temperature, and reaction time. Methanol, ethanol, and propanol are the most commonly used alcohols. In fact, biodiesel yield is independent of the type of the alcohol used and the alcohol selection depends on cost [60]. In trans-esterification, ester bonds are broken first then followed by hydroxyl bond, whereas in esterification hydroxyl bonds are broken before ester bonds resulting in glycerol as byproduct in transesterification and water in esterification [54].

Transesterification can be carried in a number of ways, using different catalytic processes. For example, it can be carried out using alcohol and alkali catalyst, acid catalyst, and biocatalyst or using alcohols in their supercritical state [39, 69]. Overall, transesterification is a sequence of three reactions; TG is first converted to a diacylglycerol (DG) and one fatty acid ester, then the DG is converted to monoacylglycerol (MG) giving an additional fatty acid ester, and finally the MG is converted to glycerol giving the last fatty acid ester.

Catalyst promotes hydrolysis of the TGs to produce fatty acids and glycerol, with the last being a byproduct. By the end of the transesterification, produced biodiesel and glycerol have to be purified in order to remove the catalyst, which requires a separation step by washing with distilled water for several times. It is well understood that catalyst selection is an important criterion.

2.1.1. Chemical Catalytic Transesterification

Alkaline Catalyst Transesterification. A base catalyst is a chemical with a pH value greater than 7. It has the ability to give extra electrons. Sodium hydroxide (NaOH), potassium hydroxide (KOH), and sodium methoxide (CH3ONa) are the most common homogeneous base catalysts employed during alkaline transesterification [11, 51, 60]. The base catalyzed process is the most commonly used because of its relative ease. It can be performed at low temperature and pressure and yields high conversion (98%) within a short time [5].

Most important limitation of the base catalysis method is the process sensitivity to both FFA and water contents. It works perfectly when the FFA and moisture contents are less than certain limits, usually below 0.5 wt% for FFA [70, 71]. In case of TGs where FFA contents exceed this limit, pre-treatment step is required. The presence of FFA promotes soap formation, which consumes the catalyst, lowers the yield, and more importantly results in difficult downstream byproducts separation and product purification [7,8]. About 60-90% of biodiesel cost comes from the high cost of the raw material [7]. In addition, alkali catalyst needs effluent treatment.

Most of the base catalyzed reactions were carried out at temperatures close to the alcohol boiling point with alcohol to oil molar ratio of 6 : 1. Akoh et al. [9] stated that to increase biodiesel yield, a stoichiometric excess of substrates (6: 1 molar ratio of methanol to oil) is favored.

Homogeneous catalysts have been used industrially for biodiesel production where produced biodiesel and glycerol have to be purified to remove the catalyst. This purification process requires large quantities of water and energy. Thus, heterogeneous catalysts have been suggested to overcome this drawback. Heterogeneous catalysts can be separated easily from the system at the end by filtration and could be reused [60, 72]. Alkaline earth oxides [73], zeolites [3], calcined hydrotalcites [18, 74], and Magnesium and Calcium oxides [16, 72] have been suggested as heterogeneous catalysts and showed good results. However, the high cost of the purified feedstock remains the main problem facing the alkaline catalyzed process.

Acid Catalyst Transesterification. The reaction of TGs and alcohol may also be catalyzed with an acid instead of a base. Most commonly used acids are strong acids like sulphuric, sulphonic, phosphoric, and hydrochloric acids [5, 8, 10].

Acid-catalyzed transesterification processes are not as popular as the base-catalyzed processes, mainly because strong acids are corrosive and the processes are too slow. Several reactions may be required in order to achieve high conversion. It has been stated that acid-catalyzed reaction may be 4000 times slower than the base catalyst process [7, 9, 54, 66]. Above that, it requires high amount of alcohol and higher concentration of catalyst. Akoh et al. [9] stated that a molar methanol: oil ratio of 30 : 1 in a range of 55-80°C with 0.5 to 1 mol% catalyst concentration is required to achieve 99% conversion in 50 h. On the other hand, acid-catalyzed processes offer an important advantage for being independent of feedstock FFA content. That is because

feedstock FFA is not converted to soap using this kind of catalysts, and hence biodiesel can be produced from low cost feedstock [6, 54].

As mentioned before, feedstock of high FFA content requires a pretreatment step if a base catalyst is to be used. This pretreatment step can be achieved using acid catalysis and methanol, where the FFA is esterified to biodiesel. When equilibrium is reached, the acid catalyst and produced water are removed from the reaction vessel by centrifugation [11]. This is followed by adding fresh methanol and base catalyst to the oil in order to catalyze the transesterification reaction.

Heterogeneous acid catalysts have been also used. This is important to avoid problems associated with homogeneous catalysts. Sulphated tin oxide has been used as superacid catalysts to transesterified waste cooking oil [22]. Sulphated zir-conia was also used as catalysts in the alcoholysis of soybean oil and in the esterification of oleic acid [21]. Heteropolyacid was used to transesterify yellow horn oil [75]. Anion and cation exchange resins were used for triolein transesterifica-tion reactions with ethanol to produce ethyl oleate [76].

2.1.2. Noncatalytic Transesterification. Although catalysts play a great role in reducing transesterification time, their presence promotes complications of final product purification. This results in increased production process cost.

To avoid catalyst drawbacks, supercritical alcohol (SCA) transesterification process was suggested [13, 51, 77]. SCA transesterification process is a catalyst free process, which provides high conversion of oil to ester in a short time. Tan et al. [78] compared SCM transesterification with conventional catalytic methods. They reported that conventional catalyst required 1 hr to convert palm oil to biodiesel, whereas SCM required only 20 min. As a result of catalyst absence, purification of the products of the transesterification reaction is much simpler and environmentally friendly compared to the previously mentioned processes.

In 2001, Saka and Kusdiana [30] conducted a research on biodiesel production from vegetable oils without any aid of catalysts. The oil-methanol mixture was heated above the supercritical temperature. Biodiesel was removed from the reaction mixture, and the excess methanol was removed by evaporation for 20min at a temperature of 90°C. It was reported that 95% conversion was achieved in the first 4 min of reaction with optimum process parameters of alcohol: oil molar ratio of 42: 1, pressure of 430 bar, and reaction temperature of 350°C. After one year (2002), Demirbas [77] studied transesterification of six different vegetable oils in supercritical methanol and reported that increasing reaction temperature to supercritical condition had favorable influence on ester conversion.

Compared to catalytic reactions, SCM reactions are fast and can achieve high conversions in a very short time. However, the reaction requires higher temperatures, pressures, and alcohol to oil molar ratio in comparison to catalytic transesterification, which result in high production cost [67, 68].

It is clearly shown that the three transesterification processes presented have several drawbacks. They are energy

intensive, recovery of byproduct is difficult, catalysts have to be removed, and waste treatment is required. To overcome these problems, enzymes have been proposed [7, 54, 79]. Most important advantage of using enzymes is their ability to convert FFA contained in the fat or oil to methyl esters completely. Additionally, glycerol, byproduct, can be easily recovered [26, 51, 80].

2.1.3. Enzymatic Transesterification. There is a great interest on using biocatalysts to catalyze TG transformation to biodiesel, which has the advantage of having low operating conditions and high product purity. Enzymatic transester-ification can be carried out at 35 to 45°C [41, 42, 81]. Contrary to chemical catalysts, enzymes do not form soaps and catalyze esterification of FFA and TG in one step without any need of the washing step. On the other hand, the major disadvantages of the enzymatic transesterification are its slower reaction rate and possible enzyme inactivation by methanol [27, 62, 82]. Lipase is an enzyme capable of catalyzing methanolysis reactions. It can be obtained from microorganisms such as bacteria and fungi. Lipases from Mucor miehei, Rhizopus oryzae, Candida antarctica, and Pseudomonas cepacia are the most commonly used enzymes [39, 62]. Lipases belong to a group of hydrolytic enzymes called hydrolases. In biological systems, lipases hydrolyze TGs to fatty acids and glycerol [66]. They work in mild conditions and have an ability to work with TGs from different origins. They have the ability to catalyze transesterification ofboth TGs and FFAs to give esters.

Extracellular and intracellular lipases are the major biocatalyst [5, 56]. Extracellular lipases refer to the recovered enzymes from the microorganism which is then purified, whereas intracellular lipases, the enzyme remains inside the producing cell walls [62]. In term of regioselectivity, lipases have been divided into three types [81]:

(i) sn-1,3-specific: hydrolyze ester bonds in positions Ri or R3 of TG,

(ii) sn-2-specific: hydrolyze ester bond in position R2 of TG,

(iii) nonspecific: do not distinguish between positions of ester.

Fjerbaek et al. [39] stated that for biodiesel production from TG, lipases should be nonstereospecific where all TG, DG, and MG can be converted to fatty acids methyl esters (FAME). In addition, they should also be able to catalyze FFA esterification.

Despite the lipases advantages over acid and base catalysts, lipases are costly which limit their industrial use [60, 83]. For that reason, reusability of the enzyme by using it in an immobilized form is essential from economic point of view.

Soluble enzyme acts as a solute in that they are dispersed in the solution and can move freely, but at the same time difficult to separate and to handle. One promising approach to overcome this difficulty is to immobilize the enzyme in a way that can be separated later by any simple separation method. Enzyme immobilization is a technique where free



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movement of the enzyme is restricted and localized to an inert support or carrier. This technique has many advantages, the most important of which is that the immobilized enzyme can be reused [40, 84]. In addition, by immobilization, the operating temperature of the process can be increased [39]. Cao [84] mentioned that an immobilized enzyme has to perform two essential functions, namely, the noncatalytic functions that are designed to aid separation and the catalytic functions that are designed to convert the targeting substrates within a desired time. This is in addition to the fact that the process is environmentally friendly and more sustainable [82].

Enzyme immobilization can be carried out in different ways. It can be classified into chemical and physical methods as shown in Figure 1. In biodiesel enzymatic production, various immobilization techniques have been used. Du et al. [24] used adsorption on macroporous resin, Noureddini et al. [27] worked on hydrophobic sol-gel support by entrapment, and Orcaire et al. [28] worked on silica aerogel by encapsulation.

Amongst all possible immobilization methods, physical adsorption has been clearly selected by most researchers due to its ease, the absence of expensive and toxic chemicals, ability to retain the activity, and feasibility of regeneration [54]. But, immobilized enzymes are also subjected to diffusion limitation (internal and external) and inactivation (mostly by methanol) [85]. These problems have been studied and solved by different researchers.

To overcome immobilized lipase inactivation, the addition of an inert solvent has been suggested. However, solvent addition is not highly recommended since this will require using solvent recovery units, which will increase production cost.

Kose and coworkers [86] investigated lipase-catalyzed transesterification of cotton seed oil with methanol in solvent-free medium. Yield of 92% was achieved in the presence of the Novozym 435 in 24 h reaction. This was

performed at 50°C, 4:1 alcohol to oil and 30% enzyme loading. In 2007, Royon et al. [87] performed comparable work for cotton seed oil using Novozym 435 at the same condition, but with using tert--butanol as solvent. They noted that tert-butanol dissolved both methanol and glycerol that might inhibit enzyme activity, and a higher conversion of 97% was observed after 24 h of reaction. Similarly, Nelson et al. [33] tested the effect of using solvent on biodiesel production yield. By using Mucor miehei lipase, yield of 94% was obtained in n-hexane system, whereas only 19% yield obtained in a solvent-free system after 8 h reaction with methanol. On the other hand, ethanol produced 65% yield in solvent-free system and 98% in n-hexane system within first 5 h of the reaction. In the same approach, using 80% tert-butanol (based on oil weight) improved biodiesel yield from soybean oil deodorizer distillate with 4% Novozym 435 from 80 to 84%. However, further increase in solvent use decreased the yield, which might result from the dilution effect on reactants [88]. Wang et al. [88] obtained same yield, 84%, when a combination of 2% Novozym 435 and 3% Lipozyme TL were used.

The importance of using solvents has been addressed well in the literature. However, as mentioned earlier solvents can be toxic, flammable, and have to be separated from the ester for reuse. Hence, efforts have been made to offer alternative solvents that are nontoxic and environmentally friendly. Candidate solvents that can replace previously mentioned solvents should have same advantages of dissolving both substrates and reduce excess alcohol inhibition and at the same time avoid the drawbacks of difficult separation of the solvent. In this regard, supercritical fluids (SCF) have been suggested as alternative solvents [89]. Further discussion on the use of SC-CO2 as a reaction medium is found in Section 4.1.2.

2.2. Biodiesel Feedstocks. Biodiesel can be synthesized from a great variety of feedstocks. These feedstocks include most

vegetable oils (soybean oil, jatropha oil, rapeseed oil, palm oil, sunflower oil, corn oil, peanut oil, canola oil, and cottonseed oil) and animal fats (tallow and lard). They can also be produced from other sources like waste cooking oil, greases, and oleaginous microorganisms with excess microbial lipid such as microalgae [13].

2.2.1. Vegetable Oils. Since vegetable oil is a feedstock that is available in large quantities, it has been widely used for the conversion to biodiesel. Majority of vegetable oils have been employed for biodiesel production such as soybean oil [44, 90], rapeseed oil [30, 80], canola oil [64], palm oil [45, 54, 91], and sunflower oil [92, 93]. However, producing biodiesel from vegetable oils competes with their use as food and involves additional land use. Also, in industrial scale, biodiesel production requires considerable use of arable lands.

2.2.2. Waste Cooking Oils. Fried oils and fats are usually broken down after a period of use and become unsuitable for further cooking as a result of increasing of FFA content. Once this reached, they are discarded or recycled. This type of feedstocks is of low cost, making them attractive for fuel production [46]. Using waste cooking oil, especially those that cannot be treated, will reduce the environment pollution. Waste cooking oil conversion into biodiesel through the transesterification process reduces their molecular weight to approximately one-third, viscosity by about one-seventh, as well as reducing their flash point and volatility [4, 51]. High oil conversion (>90%) has been reported by many investigators [94-96] in spite of the high FFA contents that range from 5 to 15 wt%.

2.2.3. Animal Fat. Animal fats are received from cattle, hog, chicken, lamb, and fish. Tallow and animal meats which are not allowed to be used as food can be used as biodiesel feedstock. However, these two sources have discontinuity problem in their supply. It is possible that suddenly a high bulk of material is available followed by a period with no supply like in the case of animal disease [48]. Animal fats are characterized by the high amount of saturated fatty acids (SFA). They are solid at room temperature and cannot be used as fuel in a diesel engine in their original form [97]. Authors of this paper had investigated possibility of biodiesel production from lamb meat fat [98] and tallow [99, 100] as feedstock.

2.2.4. Oleaginous Microorganisms. As an alternative to vegetable oils and animal fats, oleaginous microorganisms have recently attracted great attention. It has been reported that such microorganisms accumulate oils and have microbial lipid content exceeding 20% [13]. The scope of this paper is on the use of microalgae in biodiesel production.

Using algae as a feedstock has been studied worldwide by several decades. However, for biodiesel production, this was started by an 18-year National Renewable Energy Laboratory (NREL) research project [50]. The potential of using algae for biodiesel production can be seen from their ability to

produce large amount ofbiodiesel and reduce the production cost. Based on algae size, they are classified to macroalgae and microalgae. Macroalgae are large and multicellular, whereas microalgae are small and unicellular. Due to the simple cell structure, microalgae are widely used and have been accepted as promise feedstock. The following section gives more details about microalgae and their potential as feedstock for biodiesel production.

3. Microalgae

Algae that contain chlorophyll are photosynthetic microorganisms that convert inorganic carbon, such as carbon dioxide, in the presence of light, water and nutrients to algal biomass [101-106]. Majority of algae are living in aquatic (saline or freshwater) environments, whereas some of them can be found in other environments such as snow, desert soils, and hot springs [107]. They can be either autotrophic or heterotrophic. Autotrophic algae require only carbon dioxide, light, and salts to grow, whereas heterotrophic require an organic source of carbon, like glucose, as well as nutrients [105, 108-110]. However, heterotrophic algae are not as efficient as autotrophic algae for oil production [49, 111]. Autotrophic is more favorable as it does not require glucose which is a food source and at the same time fixes CO2, which has positive effect on the environment. Microalgae also can be either phototrophic or chemotrophic. Phototrophic algae use light as an energy source, whereas chemotrophic type use oxidizing compounds [107]. Additionally, some algae are capable of behaving in both autotrophic and heterotrophic modes. These are called mixotrophic algae [104, 112].

Algae range from unicellular to multicellular forms [105]. Some algae are motile while others are nonmotile. Moreover, they may exist as colonies, filaments, or amoe-boids [104]. Based on their internal structure, algae cells are generally categorized into eukaryotes and prokaryotes. Prokaryotic cells do not have nuclear membrane-bound DNA, organelles and other membranous structures as eukaryotic cells. As shown in Table 1, almost all the algae are eukaryotes. In eukaryotes, microalgae cells consist of cell wall, plasma membrane, cytoplasm, nucleus, and organelles such as mitochondria, lysosomes, and golgi.

As shown in Table 2, microalgae oil contents are usually between 20-50% of dry algae biomass weight. However, many microalgae oil content may exceed 80% of dry algae biomass weight [49, 101, 133, 134]. Besides, microalgae can grow very fast by doubling biomass in 24 hours, and during exponential growth phase they can double their biomass in about 3.5 hours [49, 111, 134, 135].

Algal species may change their composition, shape, and color based on growing culture and growth condition such as light, nutrients, temperature, and acidity, pH. It is well known that using stressful environment may cause algae to store more oil.

Unlike glycerolipids that are found in membranes under optimal conditions, many microalgae alter towards accumulations of neutral lipids in form TAG [136]. Microalgae

Table 1: Summary of different algal groups classification for different habitat types [113].

Kingdom Division Marine Freshwater Habitat Terrestrial Symbiotic

Prokaryota Cyanophyta Yes yes Yes yes

Prochlorophyta Yes yes Not detected yes

Glaucophyta Not detected yes Yes yes

Rhodophyta yes yes Yes yes

Heterokontophyta yes yes Yes yes

Eukaryota Haptophyta yes yes Yes yes

Cryptophyta yes yes Not detected yes

Chlorarachniophyta yes Not detected Not detected yes

Dinophyta yes yes Not detected yes

Euglenophyta yes yes Yes yes

Chlorophyta yes yes Yes yes

Table 2: Oil content of some common microalgae [49, 114].

Microalgae Oil content (% dry biomass weight)

Botryococcus braunii 25-80

Chlorella protothecoides 23-30

Chlorella vulgaris 14-40

Crypthecodinium cohnii 20

Cylindrotheca sp. 16-37

Dunaliella salina 14-20

Neochloris oleoabundans 35-65

Nitzschia sp. 45-47

Phaeodactylum tricornutum 20-30

Schizochytrium sp. 50-77

Spirulina maxima 4-9

Tetraselmis suecia 15-23

composition is species specific and varies between different microalgae depending on nutrient, salinity, medium pH., temperature, light intensity, and growth phase. In all cells, lipid and fatty acids are constituents that act as membrane compounds, storage product, metabolites, and energy source. It is known that under stress condition, photosynthesis activity decreases; therefore, lipid synthesis occurs. Most of microalgae-produced oils having fatty acid constitutions similar to most common vegetable oils [137].

In general, lipids may include neutral lipids (nonpolar), polar lipids, wax esters, sterols, and hydrocarbons as well phenyl derivatives [138]. Major part of nonpolar lipids of microalgae is TGs and FFA. Typically, algae lipids have a carbon number range C12-C22. Most of fatty acids found in algae lipids are straight chain with even number of carbon atoms. They may be either saturated or unsaturated [115]. Table 3 gives a summary of the range of lipid reported in different algae species.

Microalgae are classified into four main classes according to their pigment components: diatoms (Bacillario-phyceae), green algae (Chlorophyceae), blue-green algae

(Cyanophyceae), and golden algae (Chrysophyceae) [102,103, 108, 139]. Table 4 gives a brief description of each division.

Microalgae biomass contains three main components: protein, carbohydrates, and lipids and, therefore, can be used in different applications ranging from food products to biofuels. They are usually used as animal feed [140], human health food [104, 141], and asbiofertilizer [49]. Additionally, microalgae can be used for atmospheric CO2 mitigation. It was reported that there are over 40,000 species ofalgae [136], but only limited number of these have been studied and have commercial significance [142].

3.1. Potential of Using Microalgae as Feedstock for Biodiesel Production. Biodiesel production from microalgae oil is more promising and sustainable alternative to previously mentioned feedstocks (Section 2.2) [143]. Compared to plants, algae do not compete with food crops and have higher energy yields per area than terrestrial crops. They present a good source of renewable biofuels, which include methane via anaerobic digestion of algal biomass, biodiesel derived from microalgae oil, and biohydrogen via photobioproduc-tion [133, 144, 145]. The focus of this paper is on biodiesel.

Using microalgae as a fuel source is not new; it was suggested more than 60 years ago by Meier for methane production [136]. However, only recently microalgae received noticeable attention due to increasing environmental concerns. Main advantage of using microalgae as feedstock is their rapid growth potential with short biomass doubling time (3.5 hours) during exponential growth and oil content ranging from 20 to 50% dry weight of biomass for numerous microalgae species, as shown in Table 2. Other major advantages and features of using microalgae are the following.

(i) Ability to grow in nonarable land [49, 126, 144, 146, 147] where they can be cultivated on lands that is unsuitable for agriculture, that is, waste land [103, 148]. Therefore, biodiesel production would not be in any way competing with food production [106, 149].

Table 3: Fatty acid composition of lipids of different microalgae [115].

Fatty acid Spirulina platensis S. maxima Scenedesmus obliquus C. vulgaris Dunaliella b

C12: 0 0.04 traces 0.3 — —

C14: 0 0.7 0.3 0.6 0.9 —

C14: 1 0.2 0.1 0.1 2 —

C 15:0 traces traces — 1.6 —

C16: 0 45.5 45.1 16.0 20.4 41.7

C16: 1 9.6 6.8 8.0 5.8 7.3

C 16:2 1.2 traces 1.0 1.7 —

C 16:4 — — 26.0 — 3.7

C17: 0 0.3 0.2 — 2.5 —

C18: 0 1.3 1.4 0.3 15.3 2.9

C18: 1 3.8 1.9 8.0 6.6 8.8

C 18:2 14.5 14.6 6.0 1.5 15.1

a-C18:3 0.3 0.3 28.0 — 20.5

y-C18:3 21.1 20.3 — — —

C20 : 2 — — — 1.5 —

C20 : 3 0.4 0.8 — 20.8 —

Others — — 2.5 19.6 —

(ii) Can be cultivated in saline and brackish environments leading to reduction in fresh water load [111].

(iii) Daily harvesting [49, 126, 150] and short harvesting cycle [106, 111] in comparison to crop plants.

(iv) High photosynthetic efficiency due to their simple structure [111, 147, 148].

(v) Reduction in major greenhouse gas contributor, by utilizing CO2 from industrial flue gasses [49, 126, 146, 149-151]. Thereby, they are considered as CO2 fixers [152].

Table 5 compares different sources of biodiesel and their oil yield per area. Chisti [49] mentioned that in order to satisfy with the US demand for transportation fuel, the biodiesel industry would need to produce 530 billion liters annually. As can be found from Table 5, the most feasible biodiesel source for the US is microalgae.

Consequently, biodiesel production from microalgae is considered to be the best efficient feedstock for biodiesel production to displace conventional feedstock's and meet global demand of fuel [153].

To use microalgae for the production ofbiodiesel, several processes have to be carried out. These consist of strain selection, cultivation, harvesting, extraction of the oil, and production ofbiodiesel from extracted oil, in which each step can be accomplished with various technologies. These steps are detailed in the following sections.

3.2. Microalgae Oil Production Systems

3.2.1. Microalgal Strain Selection. Microalgae come in a variety of strains; each has different proportions of lipid,

protein, and carbohydrates contents. From over 3,000 collected, screened, and characterized algal strains in the National Renewable Energy laboratory (NREL) sponsored project [50], selection of the most suitable strain needs certain parameters evaluation. These parameters include oil content, growth rate and productivity, strain adaptableness, and withstanding to different weather conditions such as temperature, salinity and pH, and high CO2 sinking capacity and provide valuable coproducts [108]. Thus, right strain selection is critical.

Numerous researches have been carried out on different species tolerance. Many of them were found to be suitable for biodiesel production. As shown in Table 6, some microalgae have high lipids content such as Nannochloropsis sp., and others have high protein contents like C. protothecoides (autotrophic) while others have high carbohydrates content like Oscillatoria limnetica under normal conditions. Among possible microalgae strains for biodiesel productions are Chlorella species. As can be seen from Table 2, C. protothe-coides oil content is roughly 15% (% dry weight) under control conditions, but this can reach around 44% [154, 155], 53% [156], and 55% [120] when grown heterotrophically.

On the other hand, generally, lower oil strains grow faster than high oil strains. This is due to slow reproduction rate as a result of storing energy as oil not as carbohydrates [157]. In addition, it should be taken into consideration that some microalgae contain high levels of unsaturated fatty acids, which reduce the oxidative stability of the biodiesel produced [158-160].

Rodolfi et al. [126] have screened variety of microalgal strains by evaluating biomass productivity and lipid content in 250-mL flask laboratory cultures (Table 7). Strains that have shown some promise lipid productivity can be further

Table 4: Summary of different microalgae divisions [ 104, 113, 116].




Photosynthesis pigments












Chlorella sp.

(i) Oceans

(ii) Freshwater

(iii) Brackish water

(i) Chlorophylls a and c

(ii) B-carotene

(i) Vegetative (binary fission or fragmentation)

(ii) Asexual (akinete, exospores, endospores or homospores)

(iii) Sexual (isogamous, anisogamous or oogamous)

C. vulgaris

Green algae C. protothecoides S. obliquus Haematococcus pluvialis Nannochloris D. salina B. braunii (i) Oceans (ii) Freshwaters (iii) Moist (iv) Terrestrial habitats. (i) Chlorophylls a and b (i) Vegetative (binary fission or fragmentation) (ii) Asexual (akinete or exospores or endospores or homospores) (iii) Sexual (isogamous, anisogamous or oogamous)

Blue-green algae S. platensis Synechococcus Cyanidium Oscillatoria (i) Freshwater (ii) Marine (iii) Terrestrial (iv) Symbiotic (i) Divided in to two groups (ii) Most species have chlorophyll a as only form of chlorophyll and phycobilins as pigments (i) Vegetative (binary fission and fragmentation) (ii) Asexual (akinete or exospores or endospores and homospores)

Anabaena cylindrical (v) Associations (iii) Some have two forms of chlorophyll a and b and lack phycobilins

Isochrysis galbana (i) Fresh water (i) Chlorophylls a and b (i) Asexual (zoospores or aplanospore, hypnospores)

Golden algae Dinobryon balticum Uroglena americana (ii) Marine (iii) Terrestrial (ii) Some have chlorophylls e carotene a and c (ii) Sexual (isogamous or anisogamous or oogamous)

improved genetically. Genetic engineering can improve all aspects of algal production, harvesting, and processing for enhanced biodiesel capabilities.

3.2.2. Microalgal Biomass Production. The main way to produce microalgal biomass is the cultivation. For commercial biomass production, microalgal biomass must be easily

cultivated in the required scale. Microalgae cultivation can be carried out either via photoautotrophic methods in open systems (open-ponds) [153, 161] or closed systems (photo-bioreactors) [102, 161, 162], or via heterotrophic methods [120, 154]. All methods have their advantages and disadvantages; therefore, investigators disagree about which of the methods and systems is more favorable. Choosing best

Table 5: Comparison between different biodiesel sources [49].

Crop Oil yield (L/ha) Land area needed (Mha)a Percent of existing US cropping areaa

Corn 172 1540 846

Soybean 446 594 326

Canola 1190 223 122

Jatropha 1892 140 77

Coconut 2689 99 54

Oil palm 5950 45 24

Microalgaeb 136,900 2 1.1

Microalgaec 58,700 4.5 2.2

a For meeting 50% of all transport fuel needs of the United States.

b70% oil by wt in biomass.

c30% oil by wt in biomass.

Table 6: Chemical composition of various microalgae (% dry weight).

Microalgae Carbohydrates Protein Lipids Reference (s)

Chaetoceros muelleri 19.3 46.9 33.2 [117]

I. galbana 26.8 47.9 14.5 [118]

Chaetoceros calcitrans 27.4 36.4 15.5 [118]

Isochrysis sp. 12.9 50.8 20.7 [119]

Prymnesiophyte (NT19) 8.4 41.3 14.7 [119]

Rhodomonas (NT15) 6.0 57.2 12 [119]

Cryptomonas (CRF101) 4.4 44.2 21.4 [119]

Chaetoceros (CS256) 13.1 57.3 16.8 [119]

C. protothecoidesa 10.6 52.6 14.6 [120-122]

C. protothecoidesb 15.4 10.3 55.2 [120, 121]

Microcystis aeruginosa 11.6 30.8 12.5 [122]

Nannochloropsis sp 29.0 10.7 60.7 [123]

S. obliquus 15 50.0 9.0 [124]

Oscillatoria limnetica 50 44.0 5.0 [124]

B. braunii 18.9 17.8 61.4 [125]

Botryococcus protuberans 16.8 14.2 52.2 [125]

a Autotrophic cultivation. bHeterotrophic cultivation.

biomass production method or system depends on the selected algal strain and its integration with appropriate downstream processing which is the means for affordability and scalability of biodiesel production.

Photoautotrophic. As mentioned previously, photoautotro-phic microalgae need light and carbon dioxide as energy and carbon sources, respectively. Thus, photoautotrophic algae cultivation is carried out in the presence of light in open ponds and photobioreactors.

Open ponds are the most commonly used systems, and their structure has been well documented. Open ponds are made of a closed loop with recirculation channels. A paddle-wheel that continuously operates is usually used to prevent sedimentation and provide mixing. During daylight, the culture is fed continuously in front of the paddlewheel where

the flow begins and circulates through the loop to the harvesting point. On completion of the circulation loop, broth is harvested behind the paddlewheel [49, 102, 161, 163]. Inclined, circular, and raceway ponds are operated at large scale. On the other hand, photobioreactors are closed bioreactors, which are designed as tubular, plate, or bubble column reactors. Among these, the most common type is tubular photobioreactors. These consist of less than 0.1 m diameter transparent tubes made from plastic or glass. Tube diameter is a critical design criteria as light does not penetrate too deeply in dense culture broths [49]. This leads to O2 accumulation and thus inhibits the photosynthesis process.

Typically, open ponds are the preferred large scale cultivation system [49]. This is due to their simplicity and low construction and capital costs [163]. However, these systems are open to the atmosphere, which lead to water

Table 7: Biomass productivity, lipid content, and lipid productivity of 30 microalgal strains cultivated in 250-mL flasks [ 126].

Algal Group Microalgae strain Habitat Biomass productivity (gl-'d-1) Lipid content (%) Lipid productivity (mgHd-1)

Chaetoceros muelleri F&M-M43 Marine 0.07 33.6 21.8

C. calcitrans CS 178 Marine 0.04 39.8 17.6

P. tricornutum F&M-M 40 Marine 0.24 18.7 44.8

Skeletonoma costatum CS 181 Marine 0.08 21.0 17.4

Diatoms Skeletonoma sp. CS 252 Marine 0.09 31.8 27.3

Thalassiosira pseudonana CS 173 Marine 0.08 20.6 17.4

Chlorella sp. F&M-M48 Freshwater 0.23 18.7 42.1

Chlorella sorokiniana IAM-212 Freshwater 0.23 19.3 44.7

C. vulgaris CCAP 211/11b Freshwater 0.17 19.2 32.6

C. vulgaris F&M-M49 Freshwater 0.20 18.4 36.9

Chlorococcum sp. UMACC 112 Freshwater 0.28 19.3 53.7

Scenedesmus quadricauda Freshwater 0.19 18.4 35.1

Scenedesmus F&M-M19 Freshwater 0.21 19.6 40.8

Scenedesmus sp. DM Freshwater 0.26 21.1 53.9

Green algae Tetraselmis. suecica F&M-M33 Marine 0.32 8.5 27.0

Tetraselmis sp. F&M-M34 Marine 0.30 14.7 43.4

T. suecica F&M-M35 Marine 0.28 12.9 36.4

Ellipsoidion sp. F&M-M31 Marine 0.17 27.4 47.3

Monodus subterraneus UTEX 151 Freshwater 0.19 16.1 30.4

Nannochloropsis sp. CS 246 Marine 0.17 29.2 49.7

Nannochloropsis sp. F&M-M26 Marine 0.21 29.6 61.0

Nannochloropsis sp. F&M-M27 Marine 0.20 24.4 48.2

Nannochloropsis sp. F&M-M24 Marine 0.18 30.9 54.8

Eustigmatophytes Nannochloropsis sp. F&M-M29 Marine 0.17 21.6 37.6

Nannochloropsis sp. F&M-M28 Marine 0.17 35.7 60.9

Isochrysis sp. (T-ISO) CS 177 Marine 0.17 22.4 37.7

Isochrysis sp. F&M-M37 Marine 0.14 27.4 37.8

Prymnesiophytes Pavlova salina CS 49 Pavlova lutheri CS 182 Marine Marine 0.16 0.14 30.9 35.5 49.4 50.2

Red algae Porphyridium cruentum Marine 0.37 9.5 34.8

evaporation and unwanted species contaminations. Besides, cell's poor utilization of light and low mass productivity, due to the low CO2 deficiencies and inefficient mixing, are other limitations [151, 164]. Therefore, for water, energy, and chemicals saving purposes, photobioreactors have been proposed, but they are not yet commercialized.

Main advantages of using photobioreactors are better algal culture and environment controlling [163], large surface to volume ratio, less water evaporation, better isolation from outside contaminations, and higher mass productivity [158]. However, photobioreactors are usually made of plastic, and UV deterioration of plastic surface is the main disadvantage. In addition, biofilm formation will require periodic cleaning [165]. Table 8 shows a comparison between the two photoautotrophic cultivation methods.

For a cost-effective cultivation, a combination of the two previous mentioned systems, referred to as hybrid system,

is the most logical choice [153]. In this type of systems, microalgal strain with high oil content is grown in photobioreactors in nutrient and CO2-rich conditions firstly to promote rapid reproduction; then the microalgae enter an open system with limited nutrient to encourage oil production [166]. This process has been successfully verified by Huntley and Redalje [167].

In addition to microalgae strains influence on oil accumulation, cultivation parameters like temperature, light intensity, pH, water salinity, and nitrogen sources also influence oil production. It has been reported that the lipid content in various microalgae strains from Chlorella species increased when growing in low-nitrogen media compared to nitrogen-rich media [168, 169]. However, in these low-nitrogen media, a reduction in growth rate was reported. Similar results were also found by Widjaja et al. [170]. Since the cell needs sufficient nitrogen for growth, the cell

Table 8: Comparison between open ponds and photobioreactors.

Method Advantages Limitations

Open ponds (i) Simple (ii) Cheap (iii) Easy to operate and maintain (iv) Low capital cost (i) Poor light utilization (ii) Difficulties in light and temperature controlling (iii) Water evaporation (iv) Foreign species contaminations (v) Lower mass productivity

Photobioreactors (i) High surface to volume ratio (ii) Higher mass productivity (iii) Less contaminations (iv) Less water losses (v) Better light utilization (i) Scalability problem (ii) Costly (iii) Complex (iv) Cells damage cases (v) Biofilm formation

Table 9: Lipid content, biomass, and lipid productivities of C. vulgaris grown autotrophically and heterotrophically on different carbon sources.

Heterotrophic cultivation Acetate Glucose Autotrophic cultivation Glycerol

Biomass productivity (mgl 1 d ') 87 151 102 10

Lipid content (%) 31 23 22 38

Lipid productivity (mg L~ 1 d~ 1) 27 35 22 4

production and division may reduce in the low-nitrogen media. However, carbon metabolism continues leading to utilize more energy for oil production rather than biomass growth [50, 171].

Other factors like CO2, light intensity, and temperature also significantly affect microalgae lipid content and composition. Renaud et al. [119] investigated the effect of temperature within the range of 25 to 35°C on Rhodomonas sp., Chaetoceros sp., Cryptomonas sp., and Isochrysis sp. growth rate and lipid content. Their results showed that optimum growth temperature was 25-27°C for Rhodomonas sp., and 27-30°C for Cryptomonas sp., Chaetoceros sp., and Isochrysis sp. Only Chaetoceros sp. was able to grow at 33 and 35°C.

With the intent of providing sufficient light to the cultivation systems, open ponds are usually made shallow, and tabular reactors are made small in diameters. Tang et al. [172] studied the influence of the above mentioned parameters on Dunaliella tertiolecta growth, lipid content, and fatty acid composition. It was reported that increasing light intensity increases cell growth rate regardless of the light source. On the other hand, as for the CO2 effect, the highest growth rate was found when CO2 concentration was in the range of 2 to 6%.

Heterotrophic Cultivation. Unlike photoautotrophic mic-roalgae, heterotrophic species are cultivated in a dark environment by utilizing organic carbon as carbon and energy sources [109, 173]. Heterotrophic cultivation method depends on the microalgae ability to eliminate light requirement and assimilate organic carbon [174]. This solve light limitation problem that appears with photoautotrophic

cultivation methods. However, not all microalgae are able to assimilate the organic carbon. Thus, this cultivation method has been studied in a limited number of microalgae species [120, 154, 175]. It has been reported that heterotrophic cultivation provides high oil content and high biomass productivity [120, 121, 154, 176, 177]. Liu et al. [178] compared lipid content of Chlorella zofingiensis cultivated under heterotrophic and photoautotrophic conditions. Lipid content of 51 wt% and 26 wt% were obtained, respectively. Liang et al. [174] compared C. vulgaris cell growth rate and lipid productivity under autotrophic and heterotrophic conditions, evaluated glucose, acetate, and glycerol carbon sources uptakes. Table 9 illustrates the results obtained.

3.2.3. Harvesting Technologies. After algal cultivation, biomass needs to be separated from the culture medium using one or more solid-liquid separation steps. Due to the microalgae small size (3-30 ^m) [102, 179, 180] and cultures medium dilution (less than 1 gL ~microalgae need to be concentrated to simplify the lipid extraction step. Biomass recovery is difficult [181] and require dewatering using suitable harvesting method [49, 151, 182].

Usually, microalgae are harvested by centrifugation, filtration, or sedimentation. Sometimes these require a pretreatment, flocculation step to improve recovery efficiency [183, 184]. Table 10 summarizes the advantages and disadvantages of each method.

To conserve energy and reduce costs, algae are often harvested in a two-step process. In the first, algae are concentrated by flocculation where diluted culture is concentrated to about 2-7% total suspended solids [108, 183]. In the second step, cells are further concentrated using conventional

Table 10: Advantages and disadvantages of different microalgal harvesting methods.

Method Advantage Disadvantage

(i) High recovery yield (up to 22 TTS) (i) Flocculants may be expensive

Flocculation (ii) Low energy requirement (ii) Contamination issue may occur (iii) Marine environment high salinity may inhibit the process (iv) Long process period

(i) Reliable (i) Energy intensive

Centrifugation (ii) Corrosion resistance (iii) Easy cleaning (ii) Expensive (iii) High speed may deteriorate the cell

(iv) Rapid (iv) Cannot be used for species <30 ,wm


(i) Reliable

(ii) Able to collect species of low density

(i) Filters may need to be replaced periodically

(ii) Membrane blockage

(iii) High maintenance cost

(iv) May be slow

(v) Head loss

harvesting methods to get an algae paste of 15-25% total suspended solids [183]. Algae harvesting cost can be high due to their low mass fraction and algal cell negative charge [182]. It is reported that microalgal cell recovery accounts for at least 20-30% of total biomass production cost [184, 185]. Harvesting technique selection depends on microalgal cells size and density, biomass concentration, culture conditions, and value of target product [102, 186].

Flocculation. Flocculation is a process that collects dispersed cells into aggregate to form large particles that facilitate cell broth separation by addition of chemical additives (flocculants). It is considered as pretreatment stage preceding the main harvesting process [184]. The main problems facing the flocculation step are the high cost and toxicity of the flocculent [187].

To endorse flocculation, chemical additives that bind algae or affect interaction between algae have to be used. There are two main types of flocculants inorganic and organic polymer. A large number of chemicals have been tested as flocculants for microalgal flocculation where the most effective one was aluminum sulfate and certain cationic polymers [187]. Numerous reports have been published concerning the flocculation of algal biomass. Among them is the work of Tenney et al. [188] which looked into fresh water microalgae flocculation using organic polyelectrolytes where extent of microalgal flocculation was determined. Cationic polyelectrolyte polyamine was found to flocculate the algae successfully at an optimum dose of 2.5 mg/L.

Filtration. Filtration separation method makes use of a permeable medium that has an ability to retain the biomass and allows the liquid to pass through. Surface and depth

filtration systems are the two known types of filtration. In surface filtration, solids are deposited on the filter medium whereas in the depth type solids are deposited within the filter medium [189]. This is satisfactory for recovering large microalgae and not for algae that size approach bacterial dimension.

Sedimentation. Sedimentation is a technique that separates microalgae biomass suspension into a concentrated slurry and clear liquid based on gravity action and particle diameter. If the biomass to be separated is small in size, settling rate will be low, and flocculants addition will be inevitable. This is a low cost process; however, its reliability is low.

Centrifugation. Almost all types of microalgae can be separated from the culture medium by centrifugation. A centrifuge is mainly a sedimentation tank with an enhanced gravitational force, by centrifugation, that increases the rate of sedimentation. Biomass recovery depends on biomass residence time within centrifugal field, settling rate, and distance [184]. Centrifugal recovery can be rapid, but it is energy intensive. Nevertheless, this process is a preferred method of recovering algal cells [183, 184]. Currently, there is no low cost harvesting method for all strains. Table 10 summarizes advantages and disadvantages ofeach harvesting method.

3.2.4. Drying. Following harvesting of the algal biomass, algal slurry moisture content has to be reduced to at least 10% by drying and dehydration. Numerous methods have been employed for drying. Most common methods are sun drying, spray drying, drum drying, and freeze drying. Again,

best drying method selection depends on required operation scale and desired product value.

In biodiesel production, lipid-rich feedstock with low water content is required; therefore, microalgae drying has to be carried out. However, drying step is energy intensive, which adds to the cost complexity of the overall production process. Various drying systems differ in both energy and cost requirements.

Sun drying is an old and cheap drying method that can be performed easily by exposure to a solar radiation source. However, it takes long drying time, requires large drying surface area, and might result in loss of products. In addition, sun drying, unlike drum drying, does not have any sterilization effect of the dried sample. On the other hand, spray drying is a method that can be used for high value products, but it has the disadvantage of being expensive and might cause significant deterioration of algae [184]. In contrast, freeze drying has been commonly used by many investigators. Freeze drying has the advantage of breaking up species cells and turning them into fine powder that makes homogenization unnecessary [190]. Belarbi et al. [191] reported that freeze-dried sample can be subjected easily for oil extraction without cell disruption. Freeze driers have been used in algae lipid extraction to extract lipid from I. galbana [192], P. tricornutum [193], C. vulgaris [194], S. platensis [195], and Chlorella sp. [196]. Table 11 summarizes advantages and disadvantages of each technique. However, freeze drying is a slow process and requires very high capital investment.

3.2.5. Oil Extraction. As stated previously, effective extraction requires concentrated algae solution. Thus, a high degree of algae concentration which takes place in the harvesting step is necessary before biomass lipid extraction. Typically, there are four well-known methods to extract oil from microalgae: (1) expeller/press, (2) solvent extraction with hexane, (3) subcritical water extraction, and (4) supercritical fluid extraction.

The recovering of intracellular products like oils from microalgae is usually difficult due to the cell wall robust structure [151, 197]. Therefore, prior to lipid extraction, algae cell has to be disrupted to a degree that facilitates extraction step [184, 198]. Several methods can be used to disrupt cell membrane. They include homogenizer, bed mill, ultrasound, autoclaving, freezing, and osmotic shock [151]. Among them, homogenizers and bed mills are often preferred because of their short residence time and lower operating costs [175]. Chisti and Moo-young [197] reviewed microbial cell disruption for intracellular products.

Mechanical Extraction. Mechanical oil extraction includes expeller press and ultrasonic extraction. In pressing technique, the presser crushes and pushes the oil out of the dry microalgal biomass. Despite expeller simplicity and lower investment cost, low oil recovery yield, high power consumption, and maintenance cost are the limitations [199].

In ultrasonic technique, shock waves break the walls and release oil to solvent. These waves are created when bubbles (created by ultrasonic wave associated from ultrasonic reactor) collapse near cell wall. Ultrasonic extraction has an advantage ofbeing fast and efficient; at the same time it needs large amount of solvent, especially in case of low sample concentration. That's because at low concentrations, samples need to be extracted more than once using new fresh solvent [200].

Chemical Extraction. The well-known concept of "like dissolve like" is the basic of the Bligh and Dyer [201] solvent extraction method. This method is the most widely used for extracting lipids from microalgae, wherein hexane is one of the most widely used solvent due to its high extraction capability and low cost.

For successful lipid extraction using an organic solvent, the solvent must be able to penetrate through the matrix to contact and dissolve the lipid. When hexane is used as a solvent, it is mixed with the algal biomass and is then separated by filtration. The solvent has to be separated from the extracted oil using distillation which is energy intensive. Miao and Wu [120] reported that large amount of microalgal oil was efficiently extracted from C. protothecoides using n-hexane. Beside, cosolvent combinations have been used by many other investigators [192, 193, 202, 203]. Hexane/ethanol and hexane/isopropanol cosolvents have been commonly used in microalgal lipid extraction. The polar solvent, which is the alcohol, is first added to disrupt the algal cell membrane. This will enhance the ability of the hexane to extract almost all the lipids. The cosolvent is then removed by liquid-liquid extraction with water. The hexane solvent extraction method can also be used in combination with the oil press/expeller mechanical method. After extracting the oil from the algae using the expeller, the remaining pulp is then mixed with hexane in order to remove any remaining oil. In this combined method, more than 95% of the total oil present in the algae is extracted [204].

The selection of lipid extraction methods depends on the extraction efficiency. Therefore, a method of high performance, such as chemical extraction, is favored over the less efficient methods, such as mechanical extraction, despite the organic solvents negative environmental impacts.

To avoid the environmental impacts of using organic solvent, nontoxic solvents have been suggested, such as subcritical water (SCW) and SC-CO2. The SCW extraction operates at temperatures just below the critical temperature, 374°C, and at high pressure, usually from 10 to 60 bar, that maintains the water in liquid form. At these conditions, water becomes less polar, and lipids can be solubilized easily. Additionally, using water at subcritical condition can eliminate the dewatering step, and high-quality product within short extraction time can be achieved [205]. However, reaching the above mentioned temperature requires large energy consumption.

On the other hand, supercritical fluids extraction makes use of fluid's salvation power enhancement when reached

Table 11: Comparison between common four microalgae drying methods.

Method Advantages Disadvantage

Sun drying (i) Cheap (no running cost, low capital cost) (i) Difficult (ii) Slow (iii) Weather dependent (iv) Require large surface (v) Contamination

Spray drying (i) Fast (ii) Continuous (iii) Efficient (i) Cost intensive (ii) Species deterioration (i.e. pigments)

Drum drying (i) Fast (ii) Efficient (iii) Sterilization advantage (i) Cost intensive

Freeze drying (i) Gentle (i) Slow process (ii) Cost intensive

above their critical point. Due to supercritical carbon dioxide's preferred critical properties, low toxicity, biodegrad-ability, and availability, it has been used to extract many desired compounds from solid matrix. Other attractive point of using SC-CO2 as extraction solvent is that after extraction, solvent and product can easily be separated once the temperature and pressure are lowered to atmospheric conditions.

3.3. Microalgae Oil Production Costs. The idea of producing biodiesel from microalgae was the main focus of NREL project [50]. It is not much different from other biodiesel produced from vegetable oils, animal fats, or waste cooking oils. It was reported that biodiesel from vegetable oil and waste grease roughly costs $ 0.54 to $ 0.62/L and $ 0.34 to $ 0.42/L, respectively [206]. Chisti [49] reported that biodiesel from palm oil almost costs $ 0.66/L and in year 2006 petrodiesel average price was $ 0.49/L, which added about $ 0.14 to palm oil cost and 35% more than petrodiesel price. The objective is therefore to reduce the product cost to at least $ 0.48/L ignoring the effect of tax on biodiesel. However, the estimated cost of biodiesel increases to $ 0.72-1.4/L using microalgae with 70wt% and 30wt% (per dry-weight) oil content, respectively [49].

The high cost of biodiesel comes mainly from the high feedstock cost; 60-90% of biodiesel cost is estimated to be from the cost of the feedstock [7]. Therefore, looking for alternatives that are cheap became essential. From that point, microalgal oil production should be enhanced. Microalgae growth requires light, CO2, water, and salt utilization. To minimize production cost, oil production must rely on maximum available mentioned requirements. Therefore, using water from waste water treatment units that contain required growth nutrients and salts and diverting CO2 from power plants is desirable and beneficial. Other attributers are development of low harvesting process by genetic engineering, improvements in photobioreactors design, and coproduction of other high values products from residual biomass after lipid extraction [184].

Solid Liquid Supercritical fluid

Figure 2: Pure component phase diagram.

4. Supercritical Fluids

Supercritical fluids (SCFs) are fluids at pressures and temperatures above their critical values. Critical values represent the highest temperature and pressure at which the substance exists as a vapor and liquid in equilibrium. This can be simply clarified from supercritical fluids phase diagram (Figure 2).

As shown in Figure 2, there are three single phases, solid, liquid, and gas, where a substance may occur. If a mixture of two, or more, phases exists in these regions, a separation between the phases is distinct, as a result of the difference in properties of the different phases. In Figure 2, the solid curves between phases indicate the coexistence of two phases. On the other hand, at a point beyond the critical point neither fusion, as a result of pressure increase, nor vaporization, as a result of temperature increase, will take place, which was defined earlier as a supercritical region. Table 12 presents the values of the critical temperatures and pressures of selected fluids most commonly used as extraction solvents [127].

In the SCF state, a solvent displays properties which are intermediate to those of liquid and gaseous states; SCFs have more desirable transport properties than liquids and better solvent properties than gases. The liquid-like density of a SCF gives high solvation power and facilitates solubility while the

Table 12: Critical properties of common solvents [127].

Critical Critical pressure

temperature (°C) (bar)

Xenon 16.7 59.2

Carbon dioxide 31.1 72.8

Ethane 32.4 49.5

Nitrous oxide 36.6 73.4

Chlorodifluoromethane 96.3 50.3

Ammonia 132.4 115.0

Methanol 240.1 82.0

Water 374.4 224.1

gas-like diffusivity gives excellent transport properties, which increases the rates of transfer from the substrate matrix to the SCF solvent as compared to that of liquid organic solvents [207]. Moreover, the low viscosity of SCFs which is close to that of the gases is an additional advantage. This last property gives rapid solvent penetration into a solid matrix [208].

4.1. Supercritical Carbon Dioxide as a Candidate Solvent. The ability of supercritical carbon dioxide, SC-CO2, to extract a solute depends on the compounds functional groups, molecular weight, and polarity. Near to its critical point, CO2 is a good solvent for nonpolar to slightly polar solutes with low molecular weight. It is an inert at most conditions, inexpensive, nontoxic, and environmentally friendly [43, 209]. Moreover, when using SC-CO2 as a solvent, no solvent residue remains in the extract since CO2 is in a gas phase at the ambient conditions. The critical temperature and critical pressure of CO2 are 31.1°C and 72.8 bar, respectively, which are not extremely high. SC-CO2 has been identified as a good alternative solvent for a number of applications including separation and reaction.

4.1.1. SC-CO2: Extraction Solvent. Extraction is the process of removal of a solute from a matrix using a solvent which is able to dissolve the desired solute. This involves contacting the matrix with the solvent either in a single stage or in multiple stages for certain period oftime and then separating the solvent. During extraction period, the solute transfers from the matrix to the solvent. Required time to achieve successful extraction depends on the solubility. That depends on extraction temperature, contact area between the solute and solvent, solvent viscosity, and solvent flow rate.

Other conventional solvent extraction techniques suffer from several drawbacks such as long extraction time and high solvent consumption, in addition to being labor intensive, difficult to automate, and often require a postextraction cleanup [210]. With these drawbacks, supercritical fluid extraction, SFE, has been proposed using the extraction solvent in its supercritical state.

SCFs were first observed more than a century ago in 1822. However, it has been developed as a novel separation technique only in the past two decades. From an economical point of view and in order not to thermally alter the

properties of the extracted materials, SCFs are mostly used as in the approximate range of temperature up to 1.2 times the critical temperature, Tc, and pressure up to 3.5 times the critical pressure Pc [211].

Although a number of substances could serve as solvents, CO2 is the most common. SC-CO2 has many applications, especially in food processing, which include decaffeination of coffee and tea, production of hops extracts, flavors extract from herbs, and extraction of edible oils. Friedrich and Pryde [212] extracted oil from soybeans using SC-CO2 and achieved a yield almost to that using n-hexane. In order to extract polar compounds from a matrix, polar supercritical fluid should be used. Thus, using a nonpolar solvent, CO2 sometimes faces difficulties to extract certain compounds from a sample matrix. To overcome this limitation, modifier fluids can be used to increase extraction efficiency. Among all modifiers tested, methanol was the most commonly used by investigators such as Tonthubthimthong et al. [213] who extracted nimbin from neem seeds. Brewer et al. [214] who extracted cocaine from human hair and Aghel et al. [215] who extracted pennyroyal essential oil using SC-CO2.

Due to the attractive features of SC-CO2, it has been used and assessed to extract lipids from different strains of microalgae [128-132, 216]. Maximum yields of 13, 9, 25, 8, 6, and 3% have been reported from C. vulgaris [128, 132], C. cohnii [216], Nannochloropsis sp. [129], S. platensis [130], chlorococum sp. [131], and S. maxima [132], respectively. The lipids were extracted from dried biomass in a temperature range of 40°C-80°C and pressure range of 100-550 bars. The lower extract yield was due to the low lipid content of grown biomass.

The extraction efficiency of SC-CO2 was compared to conventional solvent extraction methods. Table 13 shows the extraction yields of lipids, defined as amount of extracted lipids per dry biomass weight, extracted from different strains of microalgae using SC-CO2, as compared to that of conventional solvent extraction. As shown, similar yields were reported when using SC-CO2 and n-hexane for extracting lipids from S. platensis [130] and S. maxima [132]. However, 25-40% lower yields were reported when comparing SC-CO2 to n-hexane and acetone extractions, from C. vulgaris [128]. A lower yield was also reported when comparing SC-CO2 and ethanol extractions from S. maxima [132]. However, other studies showed a better performance than n-hexane from chlorococum sp. and Nannochloropsis sp. [129, 131].

To further enhance the SC-CO2 extraction yields, the use of a cosolvent has been suggested. SC-CO2 with 10% ethanol as a cosolvent for lipid extraction from S. maxima has been reported [217]. By doing so, the extraction yield increased by 24% from 32% to reach 40%. This enhancement was explained by ethanol destruct effect on microalgal cellular walls.

4.1.2. SC-CO2: Reaction Media. Majority of chemical processes are carried out in organic solvents, which in most cases are toxic and flammable. Furthermore, these organic solvents need to be separated from the desired product and recycled

Table 13: Comparison of SC-CO2 performance and other conventional extraction solvents on lipids extraction yields from microalgae biomass.

Microalgae species



Other conventional solvents Ethanol



C. vulgaris Nannochloropsis sp S. platensis chlorococum sp S. maxima

13.3 25 7.8 5.8 2.5

18.5 23 7.7

3.2 2.6

back. To avoid these drawbacks, SCFs are suggested as an alternative.

As mentioned earlier, SCFs have gas-like diffusivities and low viscosities, which reduce mass resistance between reaction mixture and the catalyst and therefore result in an increase of reaction rate. Among possible solvents that can be used in supercritical conditions to conduct transesteri-fication reactions, CO2 was chosen due to its low critical temperature which make the process less energy intensive and more importantly below the denaturation temperature of the biocatalyst.

Kumar et al. [41] esterified palmitic acid with ethanol in temperature range of 35 to 70°C in the presence of three different lipases in SC-CO2. Their results showed that Novozym 435 was the best catalyst. In SC-CO2, Lipolase 100T and hog pancreas lipase showed similar results. Yields of 74, 44, and 40% were reached using Novozym 435, Lipolase 100T, and hog pancreas lipase, respectively, which were comparable to yield in solvent free system. Romero et al. [89] esterified isoamyl alcohol in SC-CO2 and n-hexane. They noted that similar esterification degree was obtained in both SC-CO2 and n-hexane systems; however, initial reaction rate was higher in SC-CO2. Laudani et al. [218] compared FFA esterification with 1-octanol over immobilized lipase from R. miehei (Lipozyme RM IM) using three different reaction media: SC-CO2, n-hexane, and solvent free systems. SC-CO2 showed the highest conversion followed by n-hexane then solvent-free system.

Although SC-CO2 has been used as a reaction media for enzyme esterification of FFA, limited work has been done on transesterification. D. Oliveira and J. V. Oliveira [219] compared enzymatic alcoholysis of palm kernel oil using n-hexane and SC-CO2 systems. In SC-CO2, highest conversion of 63% was obtained using Novozym 435 as catalyst whereas in n-hexane Lipozyme IM provided the highest conversion of 77%. Rathore and Madras [61] produced biodiesel from Jatropha oil with Novozym 435 in SC-CO2. Optimum conditions were found to be 45°C, alcohol:oil molar ratio of 5 : 1, 30% enzyme loading, and 8 h with conversions of 60-70%. Varma and Madras [220] produced biodiesel from caster and linseed oils with Novozym 435 in SC-CO2, and 45% yield in methanol and 35% in ethanol were obtained from linseed oil, whereas a very low yield of less than 10% was obtained from castor oil. Varma et al. [221] synthesized

biodiesel from mustard and sesame oils using different acyl acceptors at 50°C for 24 h reaction. Their results showed that using mustard oil, conversion of roughly 70% and 65% can be obtained using methanol and ethanol, respectively. On the other hand, using sesame oil, a conversion of round 55% was obtained from ethanol, whereas only 45% conversion was obtained with methanol.

Despite the advantages of using SC-CO2 as a reaction media for the enzymatic production of biodiesel, it has not been reported in any previous work on microalgae oil.

5. Microalgae for Biodiesel Enzymatic Production Using SC-CO2

5.1. Microalgae as a Feedstock in Conventional Process. Recently, feasibility of using microalgae to produce biodiesel, as an alternative to fossil fuels, received significant attention since they are rich in lipids. Species like C. vulgaris, C. emersonii, Nannochloropsis sp., P. tricornutum, and T. suecica have been reported in the literature for biodiesel production, where most of them were cultivated using glucose as a carbon source. However, glucose can be fermented directly to produce bioethanol.

Conventionally, microalgae have been used for biodiesel production using chemical catalytic reactions. Miao and Wu [120] studied biodiesel production from heterotrophic cultivated microalgae oil from C. protothecoides by 100% H2SO4 (based on oil weight) acidic transesterification. Biodiesel optimum conversion yield of 63% was obtained with 56 : 1 methanol: oil molar ratio at 30°C in 4 h reaction time. To overcome disadvantages of homogeneous catalysts, Carrero et al. [222] tested the ability of using hierarchical zeolites as heterogeneous catalyst.

With the target to reduce biodiesel production cost associated with oil extraction cost, in-situ transesterification, which is a direct conversion without solvent extraction, of the biomass oil to biodiesel has been performed [223,224]. A conversion of 91% was achieved after 8 h of reaction at 60° C from Chlorella sp. [223] and 39, 40, 77, 78, and 82% were obtained from Synechocystis sp. PCC 6803 Synechococcus elongates, Chlorella sorokiniana, T. suecica, and Chaetoceros gracilis at 80°C [224]. The high conversion obtained with Chlorella species could be due to the use of a stirring

reactor that enhanced the mixing and reduced mass transfer resistances.

5.2. Enzymatic Biodiesel Production from Microalgae. Similar to conventional feedstocks conversion, microalgae oil can also be converted to biodiesel using lipase. In this perspective, C. protothecoides is the only species that has been tested so far. Xiong et al. [225] produced biodiesel with 98% conversion from C. protothecoides with 30 wt% of Candida sp. lipase. Reaction conditions were 3 : 1 methanol: oil molar ratio, 10% water content, 38°C, pH of 7, and 12 h reaction. Similar conversion was obtained by Li et al. [154] at similar conditions but using 75 wt% of the immobilized lipase rather than 30wt%. C. protothecoides was cultivated heterotrophically in both studies using glucose.

5.3. Enzymatic Production with SC-CO2 Reaction Medium. To overcome the lipase inhibition limitations, mainly by methanol and glycerol, chemical solvents that can dissolve both methanol and glycerol have the advantage of increasing conversion yield. However, the use of organic solvents is not recommended due to its harmful environmental input and the solvent extraction unit.

Using SC-CO2 as a reaction media adds to the advantages of organic solvents in saving downstream processing cost where product purification is not necessary. Since solubility is greatly influenced by fluid temperature and pressure adjustments, separation can be easily achieved by a pressure reduction where the product and enzyme do not dissolve at room temperature.

Due to its advantages over conventional organic solvents, the application of the high cost SC-CO2 process may be justified in oil extraction from microalgae. However, its justification for biodiesel production may not be evident, despite its positive effect on reducing inhibition effects and easy product separation. Nevertheless, a combined continuous process of extracting oil from microalgae using SC-CO2 and the use of the extracted oil for biodiesel production using immobilized lipase in SC-CO2 in a one integrated system would economically be feasible. In this continuous process, the oil that is extracted from microalgae is already dissolved in SC-CO2 and can be fed directly to the enzymatic bioreactor to produce biodiesel without the need for further expensive pumping. In this way, the attractive advantages of performing the reaction in SC-CO2 media will be gained, avoiding at the same time the disadvantage of high pumping cost. Besides, using high pressure CO2 might not have significant negative effect of lipase stability. Lanza et al. [226] investigated the influence of SC-CO2 pressure on lipase activity and reported that the residual activity of Novozym-435 was approximately 90%. Previous study of D. Oliveira and J. V. Oliveira [219] on converting palm kernel oil to biodiesel using Novozym 435 showed that the rise in pressure in the range 60-90 bar actually results in an enhancement of initial reaction rate and conversion. However, at pressures beyond but 200 bar, a change in lipase structure may occur, which has a negative effect on the reaction. Therefore, the

application of SC-CO2 in the enzymatic reaction system should not exceed 200 bar.

6. Conclusions

As verified in this paper, biodiesel produced from microalgae can realistically satisfy the global demand of diesel-fuel requirements. However, for cost effective production, this will not be applicable without microalgae biology and production processes enhancements. The potential of microalgal biodiesel production depends on selected microalgal strain and its ability to live in saline or use wastewaters and utilize CO2 as a sole carbon source. In addition, biomass recovery that usually requires high energy and oil extraction has to be optimized for effective low cost overall process production. Another important point to be taken into consideration is the ability to use spent biomass, after oil extraction, for the production of other valuable coproducts such as animal feed or fertilizers.

The paper presents SC-CO2 as a promising oil extraction technique from microalgae, and lipase as a biocatalyst for biodiesel production instead of the conventional chemical catalysts that require feed purification. The use of SC-CO2 as a reaction media for the enzymatic production of biodiesel has also been discussed in the paper. Authors of this review, suggest future work to be done on designing an integrated SC-CO2 extraction/reaction process, whereby a stream of extracted oil-rich SC-CO2 from selected microalgae species is fed to a bioreactor containing lipase for enzymatic conversion of the oil into biodiesel.


[1] A. K. Agarwal, "Biofuels (alcohols and biodiesel) applications as fuels for internal combustion engines," Progress in Energy and Combustion Science, vol. 33, no. 3, pp. 233-271, 2007.

[2] E. G. Shay, "Diesel fuel from vegetable oils: status and opportunities," Biomass and Bioenergy, vol. 4, no. 4, pp. 227242, 1993.

[3] G. R. Peterson and W. P. Scarrah, "Rapeseed oil transesteri-fication by heterogeneous catalysis," Journal of the American Oil Chemists Society, vol. 61, no. 10, pp. 1593-1597, 1984.

[4] A. Demirbas, "Biodiesel from waste cooking oil via base-catalytic and supercritical methanol transesterification," Energy Conversion and Management, vol. 50, no. 4, pp. 923927, 2009.

[5] H. Fukuda, A. Kondo, and H. Noda, "Biodiesel fuel production by transesterification of oils," Journal of Bioscience and Bioengineering, vol. 92, no. 5, pp. 405-416, 2001.

[6] Y. Zhang, M. A. Dube, D. D. McLean, and M. Kates, "Biodiesel production from waste cooking oil: 1. Process design and technological assessment," Bioresource Technology, vol. 89, no. 1, pp. 1-16, 2003.

[7] S. Al-Zuhair, "Production of biodiesel: possibilities and challenges," Biofuels, Bioproducts and Biorefining, vol. 1, no. 1,pp. 57-66, 2007.

[8] F. Ma and M. A. Hanna, "Biodiesel production: a review," Bioresource Technology, vol. 70, no. 1, pp. 1-15, 1999.

[9] C. C. Akoh, S. W. Chang, G. C. Lee, and J. F. Shaw, "Enzymatic approach to biodiesel production," Journal of Agricultural and Food Chemistry, vol. 55, no. 22, pp. 8995-9005, 2007.

[10] L. C. Meher, D. Vidya Sagar, and S. N. Naik, "Technical aspects of biodiesel production by transesterification—a review," Renewable and Sustainable Energy Reviews, vol. 10, no. 3, pp. 248-268, 2006.

[11] Z. Helwani, M. R. Othman, N. Aziz, W. J. N. Fernando, and J. Kim, "Technologies for production of biodiesel focusing on green catalytic techniques: a review," Fuel Processing Technology, vol. 90, no. 12, pp. 1502-1514, 2009.

[12] B. Freedman, E. H. Pryde, and T. L. Mounts, "Variables affecting the yields of fatty esters from transesterified vegetable oils," Journal of the American Oil Chemists Society, vol. 61, no. 10, pp. 1638-1643, 1984.

[13] A. Demirbas, "Progress and recent trends in biofuels," Progress in Energy and Combustion Science, vol. 33, no. 1, pp. 1-18,2007.

[14] L. G. Schumacher, W. Marshall, J. Krahl, W. B. Wetherell, and M. S. Grabowski, "Biodiesel emissions data from series 60 DDC engines," Transactions of the American Society of Agricultural Engineers, vol. 44, no. 6, pp. 1465-1468, 2001.

[15] D. Darnoko and M. Cheryan, "Kinetics of palm oil transesterification in a batch reactor," Journal of the American Oil Chemists' Society, vol. 77, no. 12, pp. 1263-1267, 2000.

[16] T. F. Dossin, M. F. Reyniers, R. J. Berger, and G. B. Marin, "Simulation of heterogeneously MgO-catalyzed transesterification for fine-chemical and biodiesel industrial production," Applied Catalysis B, vol. 67, no. 1-2, pp. 136-148, 2006.

[17] B. Freedman, R. O. Butterfield, and E. H. Pryde, "Transesterification kinetics of soybean oil 1," Journal of the American Oil Chemists' Society, vol. 63, no. 10, pp. 1375-1380, 1986.

[18] W. Xie, H. Peng, and L. Chen, "Calcined Mg-Al hydrotalcites as solid base catalysts for methanolysis of soybean oil," Journal of Molecular Catalysis B, vol. 246, no. 1-2, pp. 24-32, 2006.

[19] H. N. Bhatti, M. A. Hanif, M. Qasim, and Ata-ur-Rehman, "Biodiesel production from waste tallow," Fuel, vol. 87, no. 13-14, pp. 2961-2966, 2008.

[20] M. Canakci and J. Van Gerpen, "Biodiesel production from oils and fats with high free fatty acids," Transactions of the American Society of Agricultural Engineers, vol. 44, no. 6, pp. 1429-1436, 2001.

[21] C. M. Garcia, S. Teixeira, L. L. Marciniuk, and U. Schuchardt, "Transesterification of soybean oil catalyzed by sulfated zirconia," Bioresource Technology, vol. 99, no. 14, pp. 66086613, 2008.

[22] M. K. Lam, K. T. Lee, and A. R. Mohamed, "Sulfated tin oxide as solid superacid catalyst for transesterification of waste cooking oil: an optimization study," Applied Catalysis B, vol. 93, no. 1-2, pp. 134-139, 2009.

[23] S. Zheng, M. Kates, M. A. Dube, and D. D. McLean, "Acid-catalyzed production of biodiesel from waste frying oil," Biomass and Bioenergy, vol. 30, no. 3, pp. 267-272, 2006.

[24] W. Du, Y. Xu, D. Liu, and J. Zeng, "Comparative study on lipase-catalyzed transformation of soybean oil for biodiesel production with different acyl acceptors," Journal of Molecular Catalysis B, vol. 30, no. 3-4, pp. 125-129, 2004.

[25] A.-F. Hsu, K. Jones, W. N. Marmer, and T. A. Foglia, "Production of alkyl esters from tallow and grease using

lipase immobilized in a phyllosilicate sol-gel," Journal of the American Oil Chemists' Society, vol. 78, no. 6, pp. 585-588, 2001.

[26] M. K. Modi, J. R. C. Reddy, B. V. S. K. Rao, and R. B. N. Prasad, "Lipase-mediated conversion of vegetable oils into biodiesel using ethyl acetate as acyl acceptor," Bioresource Technology, vol. 98, no. 6, pp. 1260-1264, 2007.

[27] H. Noureddini, X. Gao, and R. S. Philkana, "Immobilized Pseudomonas cepacia lipase for biodiesel fuel production from soybean oil," Bioresource Technology, vol. 96, no. 7, pp. 769-777, 2005.

[28] O. Orcaire, P. Buisson, and A. C. Pierre, "Application of silica aerogel encapsulated lipases in the synthesis of biodiesel by transesterification reactions," Journal of Molecular Catalysis B, vol. 42, no. 3-4, pp. 106-113, 2006.

[29] S. Shah and M. N. Gupta, "Lipase catalyzed preparation of biodiesel from Jatropha oil in a solvent free system," Process Biochemistry, vol. 42, no. 3, pp. 409-414, 2007.

[30] S. Saka and D. Kusdiana, "Biodiesel fuel from rapeseed oil as prepared in supercritical methanol," Fuel, vol. 80, no. 2, pp. 225-231,2001.

[31] G. Madras, C. Kolluru, and R. Kumar, "Synthesis of biodiesel in supercritical fluids," Fuel, vol. 83, no. 14-15, pp. 20292033, 2004.

[32] J. M. N. van Kasteren and A. P. Nisworo, "A process model to estimate the cost of industrial scale biodiesel production from waste cooking oil by supercritical transesterification," Resources, Conservation and Recycling, vol. 50, no. 4, pp. 442458, 2007.

[33] L. A. Nelson, T. A. Foglia, and W. N. Marmer, "Lipase-catalyzed production of biodiesel," Journal of the American Oil Chemists' Society, vol. 73, no. 9, pp. 1191-1195, 1996.

[34] R. D. Abigor, P. O. Uadia, T. A. Foglia et al., "Lipase-catalysed production of biodiesel fuel from some Nigerian lauric oils," Biochemical Society Transactions, vol. 28, no. 6, pp. 979-981, 2000.

[35] M. Kaieda, T. Samukawa, A. Kondo, and H. Fukuda, "Effect of methanol and water contents on production of biodiesel fuel from plant oil catalyzed by various lipases in a solventfree system," Journal of Bioscience and Bioengineering, vol. 91, no. 1,pp. 12-15, 2001.

[36] C. J. Shieh, H. F. Liao, and C. C. Lee, "Optimization of lipase-catalyzed biodiesel by response surface methodology," Bioresource Technology, vol. 88, no. 2, pp. 103-106, 2003.

[37] M. Mittelbach, "Lipase catalyzed alcoholysis of sunflower oil," Journal of the American Oil Chemists' Society, vol. 67, no. 3, pp. 168-170, 1990.

[38] K. R. Jegannathan, S. Abang, D. Poncelet, E. S. Chan, and P. Ravindra, "Production of biodiesel using immobilized lipase—a critical review," Critical Reviews in Biotechnology, vol. 28, no. 4, pp. 253-264, 2008.

[39] L. Fjerbaek, K. V. Christensen, and B. Norddahl, "A review of the current state of biodiesel production using enzymatic transesterification," Biotechnology and Bioengineering, vol. 102, no. 5, pp. 1298-1315, 2009.

[40] M. Iso, B. Chen, M. Eguchi, T. Kudo, and S. Shrestha, "Production of biodiesel fuel from triglycerides and alcohol using immobilized lipase," Journal of Molecular Catalysis B, vol. 16, no. 1, pp. 53-58, 2001.

[41] R. Kumar, G. Madras, and J. Modak, "Enzymatic synthesis of ethyl palmitate in supercritical carbon dioxide," Industrial

and Engineering Chemistry Research, vol. 43, no. 7, pp. 15681573, 2004.

[42] M. G. De Paola, E. Ricca, V. Calabro, S. Curcio, and G. Iorio, "Factor analysis of transesterification reaction of waste oil for biodiesel production," Bioresource Technology, vol. 100, no. 21, pp. 5126-5131,2009.

[43] M. Mukhopadhyay, Natural Extracts Using Supercritical Carbon Dioxide, CRC Press, New York, NY, USA, 2000.

[44] W. M. Antunes, C. D. O. Veloso, and C. A. Henriques, "Transesterification of soybean oil with methanol catalyzed by basic solids," Catalysis Today, vol. 133-135, no. 1-4, pp. 548-554, 2008.

[45] M. A. Kalam and H. H. Masjuki, "Biodiesel from palmoil— an analysis of its properties and potential," Biomass and Bioenergy, vol. 23, no. 6, pp. 471-479, 2002.

[46] A. N. Phan and T. M. Phan, "Biodiesel production from waste cooking oils," Fuel, vol. 87, no. 17-18, pp. 3490-3496, 2008.

[47] A. Srivastava and R. Prasad, "Triglycerides-based diesel fuels," Renewable & Sustainable Energy Reviews, vol. 4, no. 2, pp. 111-133,2000.

[48] D. Rutz and R. Janssen, BioFuel Technology Handbook, WIP Renewable Energies, 2007.

[49] Y. Chisti, "Biodiesel from microalgae," Biotechnology Advances, vol. 25, no. 3, pp. 294-306, 2007.

[50] J. Sheehan et al., A Look Back at the U.S. Department of Energy's Aquatic Species Program: Biodiesel from Algae, National Renewable Energy Laboratory, 1998.

[51] A. Demirbas, "Progress and recent trends in biodiesel fuels," Energy Conversion and Management, vol. 50, no. 1, pp. 14-34, 2009.

[52] D. Bajpai and V. K. Tyagi, "Biodiesel: source, production, composition, properties and its benifits," Journal of Oleo Science, vol. 55, no. 10, pp. 487-502, 2006.

[53] P. Fellows, Food ProcessingTechnology: Principles and Practice, Woodhead Publishing Limited and CRC Press LLC, 2000.

[54] S. Al-Zuhair, F. W. Ling, and L. S. Jun, "Proposed kinetic mechanism of the production of biodiesel from palm oil using lipase," Process Biochemistry, vol. 42, no. 6, pp. 951-960, 2007.

[55] A. Demirbas, "Importance of biodiesel as transportation fuel," Energy Policy, vol. 35, no. 9, pp. 4661-4670, 2007.

[56] S. V. Ranganathan, S. L. Narasimhan, and K. Muthukumar, "An overview of enzymatic production of biodiesel," Bioresource Technology, vol. 99, no. 10, pp. 3975-3981, 2008.

[57] M. A. Hess, M. J. Haas, T. A. Foglia, and W. N. Marmer, "Effect of antioxidant addition on NOx emissions from biodiesel," Energy & Fuels, vol. 19, no. 4, pp. 1749-1754,2005.

[58] W. G. Wang, D. W. Lyons, N. N. Clark, M. Gautam, and P. M. Norton, "Emissions from nine heavy trucks fueled by diesel and biodiesel blend without engine modification," Environmental Science & Technology, vol. 34, no. 6, pp. 933939, 2000.

[59] S. A. Basha, K. R. Gopal, and S. Jebaraj, "A review on biodiesel production, combustion, emissions and performance," Renewable and Sustainable Energy Reviews, vol. 13, no. 6-7, pp. 1628-1634, 2009.

[60] Y. C. Sharma, B. Singh, and S. N. Upadhyay, "Advancements in development and characterization of biodiesel: a review," Fuel, vol. 87, no. 12, pp. 2355-2377, 2008.

[61] V. Rathore andG. Madras, "Synthesis of biodiesel from edible and non-edible oils in supercritical alcohols and enzymatic

synthesis in supercritical carbon dioxide," Fuel, vol. 86, no. 17-18, pp. 2650-2659, 2007.

[62] A. Robles-Medina, P. A. Gonzalez-Moreno, L. Esteban-Cerdan, and E. Molina-Grima, "Biocatalysis: towards ever greener biodiesel production," Biotechnology Advances, vol. 27, no. 4, pp. 398-408, 2009.

[63] X. Fan and R. Burton, "Recent development of biodiesel feedstocks and the applications of glycerol: a review," The Open Fuels & Energy Science Journal, vol. 1, pp. 100-109,

[64] M. A. Dube, A. Y. Tremblay, and J. Liu, "Biodiesel production using a membrane reactor," Bioresource Technology, vol. 98, no. 3, pp. 639-647, 2007.

[65] J. Van Gerpen, "Biodiesel processing and production," Fuel Processing Technology, vol. 86, no. 10, pp. 1097-1107, 2005.

[66] J. M. Marchetti, V. U. Miguel, and A. F. Errazu, "Possible methods for biodiesel production," Renewable and Sustainable Energy Reviews, vol. 11, no. 6, pp. 1300-1311,2007.

[67] S. Sinha, A. K. Agarwal, and S. Garg, "Biodiesel development from rice bran oil: transesterification process optimization and fuel characterization," Energy Conversion and Management, vol. 49, no. 5, pp. 1248-1257, 2008.

[68] K. Rajan and K. R. Senthilkumar, "Effect of exhaust gas recirculation (EGR) on the performance and emission characteristics of diesel engine with sunflower oil methyl ester," Jordan Journal of Mechanical and Industrial Engineering, vol. 3, no. 4, pp. 306-311,2009.

[69] L. Lin, D. Ying, S. Chaitep, and S. Vittayapadung, "Biodiesel production from crude rice bran oil and properties as fuel," Applied Energy, vol. 86, no. 5, pp. 681-688, 2009.

[70] F. Ma, L. D. Clements, and M. A. Hanna, "Biodiesel fuel from animal fat. Ancillary studies on transesterification of beef tallow," Industrial and Engineering Chemistry Research, vol. 37, no. 9, pp. 3768-3771, 1998.

[71] A. Sivasamy, K. Y. Cheah, P. Fornasiero, F. Kemausuor, S. Zinoviev, and S. Miertus, "Catalytic applications in the production of biodiesel from vegetable oils," ChemSusChem, vol. 2, no. 4, pp. 278-300, 2009.

[72] M. L. Granados, M. D. Z. Poves, D. M. Alonso et al., "Biodiesel from sunflower oil by using activated calcium oxide," Applied Catalysis B, vol. 73, no. 3, pp. 317-326, 2007.

[73] T. Ebiura, T. Echizen, A. Ishikawa, K. Murai, and T. Baba, "Selective transesterification of triolein with methanol to methyl oleate and glycerol using alumina loaded with alkali metal salt as a solid-base catalyst," Applied Catalysis A, vol. 283, no. 1-2, pp. 111-116, 2005.

[74] C. C. C. M. Silva, N. F. P. Ribeiro, M. M. V. M. Souza, and D. A. G. Aranda, "Biodiesel production from soybean oil and methanol using hydrotalcites as catalyst," Fuel Processing Technology, vol. 91, no. 2, pp. 205-210, 2010.

[75] S. Zhang, Y. G. Zu, Y. J. Fu, M. Luo, D. Y. Zhang, and T. Efferth, "Rapid microwave-assisted transesterification of yellow horn oil to biodiesel using a heteropolyacid solid catalyst," Bioresource Technology, vol. 101, no. 3, pp. 931-936,

[76] N. Shibasaki-Kitakawa, H. Honda, H. Kuribayashi, T. Toda, T. Fukumura, and T. Yonemoto, "Biodiesel production using anionic ion-exchange resin as heterogeneous catalyst," Bioresource Technology, vol. 98, no. 2, pp. 416-421, 2007.

[77] A. Demirbas, "Biodiesel from vegetable oils via transesterification in supercritical methanol," Energy Conversion and Management, vol. 43, no. 17, pp. 2349-2356, 2002.

[78] K. T. Tan, K. T. Lee, and A. R. Mohamed, "Production of FAME by palm oil transesterification via supercritical methanol technology," Biomass and Bioenergy, vol. 33, no. 8, pp. 1096-1099,2009.

[79] M. J. Haas and T. A. Foglia, "Alternate feedstocks and technologies for biodiesel production," in The Biodiesel Handbook, G. Knothe, J. V. Gerpen, and J. Krahl, Eds., pp. 42-61, AOCS Press, Champaign, III, USA, 2005.

[80] L. Li, W. Du, D. Liu, L. Wang, and Z. Li, "Lipase-catalyzed transesterification of rapeseed oils for biodiesel production with a novel organic solvent as the reaction medium," Journal of Molecular Catalysis B, vol. 43, no. 1-4, pp. 58-62, 2006.

[81] M. Szczesna Antczak, A. Kubiak, T. Antczak, and S. Bielecki, "Enzymatic biodiesel synthesis—key factors affecting efficiency of the process," Renewable Energy, vol. 34, no. 5, pp. 1185-1194, 2009.

[82] K. R. Jegannathan et al., "Design an immobilized lipase enzyme for biodiesel production," Journal of Renewable Sustainable Energy, vol. 1, no. 6, p. 063101, 2009.

[83] V. Caballero, F. M. Bautista, J. M. Campelo et al., "Sustainable preparation of a novel glycerol-free biofuel by using pig pancreatic lipase: partial 1,3-regiospecific alcoholysis of sunflower oil," Process Biochemistry, vol. 44, no. 3, pp. 334342, 2009.

[84] L. Cao, "Immobilised enzymes: science or art?" Current Opinion in Chemical Biology, vol. 9, no. 2, pp. 217-226, 2005.

[85] C. M. Drapcho, N. P. Nhuan, and T. H. Walker, Biofuels Engineering Process Technology, McGraw-Hill Companies, 2008.

[86] O. Kose, M. Tuter, and H. A. Aksoy, "Immobilized Candida antarctica lipase-catalyzed alcoholysis of cotton seed oil in a solvent-free medium," Bioresource Technology, vol. 83, no. 2, pp. 125-129,2002.

[87] D. Royon, M. Daz, G. Ellenrieder, and S. Locatelli, "Enzymatic production of biodiesel from cotton seed oil using t-butanol as a solvent," Bioresource Technology, vol. 98, no. 3, pp. 648-653, 2007.

[88] L. Wang, W. Du, D. Liu, L. Li, and N. Dai, "Lipase-catalyzed biodiesel production from soybean oil deodorizer distillate with absorbent present in tert-butanol system," Journal of Molecular Catalysis B, vol. 43, no. 1-4, pp. 29-32, 2006.

[89] M. D. Romero et al., "Enzymatic synthesis of isoamyl acetate with immobilized Candida antarctica lipase in supercritical carbon dioxide," Journal of Supercritical Fluids, vol. 33, no. 1, pp. 77-84, 2005.

[90] X. Liu, H. He, Y. Wang, S. Zhu, and X. Piao, "Transesterifi-cation of soybean oil to biodiesel using CaO as a solid base catalyst," Fuel, vol. 87, no. 2, pp. 216-221, 2008.

[91] A. Z. Abdullah, B. Salamatinia, H. Mootabadi, and S. Bhatia, "Current status and policies on biodiesel industry in Malaysia as the world's leading producer of palm oil," Energy Policy, vol. 37, no. 12, pp. 5440-5448, 2009.

[92] G. A. Pereyra-Irujo, N. G. Izquierdo, M. Covi, S. M. Nolasco, F. Quiroz, and L. A. N. Aguirrezabal, "Variability in sunflower oil quality for biodiesel production: a simulation study," Biomass and Bioenergy, vol. 33, no. 3, pp. 459-468, 2009.

[93] K. G. Georgogianni, M. G. Kontominas, P. J. Pomonis, D. Avlonitis, and V. Gergis, "Conventional and in situ transesterification of sunflower seed oil for the production of biodiesel," Fuel Processing Technology, vol. 89, no. 5, pp. 503-509, 2008.

[94] Z. Wen, X. Yu, S. T. Tu, J. Yan, and E. Dahlquist, "Biodiesel production from waste cooking oil catalyzed by TiO2-MgO

mixed oxides," Bioresource Technology, vol. 101, no. 24, pp. 9570-9576, 2010.

[95] P. Patil, S. Deng, J. Isaac Rhodes, and P. J. Lammers, "Conversion of waste cooking oil to biodiesel using ferric sulfate and supercritical methanol processes," Fuel, vol. 89, no. 2, pp. 360-364, 2010.

[96] Y. Wang, S. O. Pengzhan Liu, and Z. Zhang, "Preparation of biodiesel from waste cooking oil via two-step catalyzed process," Energy Conversion and Management, vol. 48, no. 1, pp. 184-188, 2007.

[97] D. Y. C. Leung, X. Wu, and M. K. H. Leung, "A review on biodiesel production using catalyzed transesterification," Applied Energy, vol. 87, no. 4, pp. 1083-1095, 2010.

[98] H. Taher et al., "Extracted fat from lamb meat by supercritical CO2 as feedstock for biodiesel production," Biochemical Engineering Journal, vol. 55, no. 1, pp. 23-31, 2011.

[99] S. Behzadi and M. M. Farid, "Production of biodiesel using a continuous gas-liquid reactor," Bioresource Technology, vol. 100, no. 2, pp. 683-689, 2009.

[100] S. T. Hoh and M. Farid, "Examining glycerolysis as a pre-treatment method for low quality biodiesel feedstock," in Proceedings of the Chemeca, Adelaide, Australia, September 2010.

[101] M. Adamczak, U. T. Bornscheuer, and W. Bednarski, "The application of biotechnological methods for the synthesis of biodiesel," European Journal of Lipid Science and Technology, vol. 111, no. 8, pp. 800-813, 2009.

[102] A. Demirbas, "Use of algae as biofuel sources," Energy Conversion and Management, vol. 51, no. 12, pp. 2738-2749, 2010.

[103] A. Demirbas and M. Fatih Demirbas, "Importance of algae oil as a source of biodiesel," Energy Conversion and Management, vol. 52, no. 1,pp. 163-170, 2011.

[104] L. E. Graham and L. W. Wilcox, Algae, Prentice Hall, Upper Saddle River, NJ, USA, 2000.

[105] G. Pokoo-Aikins, A. Nadim, M. M. El-Halwagi, and V. Mahalec, "Design and analysis of biodiesel production from algae grown through carbon sequestration," Clean Technologies and Environmental Policy, vol. 12, no. 3, pp. 239-254, 2010.

[106] A. P. Vyas, J. L. Verma, and N. Subrahmanyam, "A review on FAME production processes," Fuel, vol. 89, no. 1, pp. 1-9, 2010.

[107] R. E. Lee, Phycology, Cambridge University Press, New York, NY, USA, 4th edition, 2008.

[108] L. Brennan and P. Owende, "Biofuels from microalgae— a review of technologies for production, processing, and extractions of biofuels and co-products," Renewable and Sustainable Energy Reviews, vol. 14, no. 2, pp. 557-577, 2010.

[109] Y.-K. Lee, "Microalgal mass culture systems and methods: their limitation and potential," Journal of Applied Phycology, vol. 13, no. 4, pp. 307-315, 2001.

[110] J. N. Rosenberg, G. A. Oyler, L. Wilkinson, and M. J. Betenbaugh, "A green light for engineered algae: redirecting metabolism to fuel a biotechnology revolution," Current Opinion in Biotechnology, vol. 19, no. 5, pp. 430-436, 2008.

[111] V. Patil, K.-Q. Tran, and H. R. Giselrad, "Towards sustainable production of biofuels from microalgae," International Journal of Molecular Sciences, vol. 9, no. 7, pp. 1188-1195, 2008.

[112] K. W. Crane and J. P. Grover, "Coexistence of mixotrophs, autotrophs, and heterotrophs in planktonic microbial communities," Journal of Theoretical Biology, vol. 262, no. 3, pp. 517-527, 2010.

[113] L. Barsanti and P. Gualtieri, Algae: Anatomy, Biochemistry, and Biotechnology, Taylor & Francis Group, CRC Press, New York, NY, USA, 2006.

[114] L. Gouveia and A. C. Oliveira, "Microalgae as a raw material for biofuels production," Journal of Industrial Microbiology & Biotechnology, vol. 36, no. 2, pp. 269-274, 2009.

[115] W. Becker, "Microalgae in human and animal nutrition," in Handbook of Microalgal Culture: Biotechnology and Applied Phycology, A. Richmond, Ed., pp. 312-351, Blackwell Science, 2004.

[116] P. Sze, A Biology of the Algae, vol. 3rd, McGraw-Hill Science, 1998.

[117] D. Voltolina, M. D. P. Sánchez-Saavedra, and L. M. Torres-Rodriguez, "Outdoor mass microalgae production in Bahia Kino, Sonora, NW Mexico," Aquacultural Engineering, vol. 38, no. 2, pp. 93-96, 2008.

[118] F. M. I. Natrah, F. M. Yusoff, M. Shariff, F. Abas, and N.

5. Mariana, "Screening of Malaysian indigenous microalgae for antioxidant properties and nutritional value," Journal of Applied Phycology, vol. 19, no. 6, pp. 711-718, 2007.

[119] S. M. Renaud, L. V. Thinh, G. Lambrinidis, and D. L. Parry, "Effect of temperature on growth, chemical composition and fatty acid composition of tropical Australian microalgae grown in batch cultures," Aquaculture, vol. 211, no. 1-4, pp. 195-214, 2002.

[120] X. Miao and Q. Wu, "Biodiesel production from heterotrophic microalgal oil," Bioresource Technology, vol. 97, no.

6, pp. 841-846, 2006.

[121] X. Miao and Q. Wu, "High yield bio-oil production from fast pyrolysis by metabolic controlling of Chlorella protothecoides," Journal of Biotechnology, vol. 110, no. 1, pp. 85-93, 2004.

[122] X. Miao, Q. Wu, and C. Yang, "Fast pyrolysis of microalgae to produce renewable fuels," Journal ofAnalytical andApplied Pyrolysis, vol. 71, no. 2, pp. 855-863, 2004.

[123] J. Fabregas, A. Maseda, A. Domínguez, and A. Otero, "The cell composition of Nannochloropsis sp. changes under different irradiances in semicontinuous culture," World Journal of Microbiology and Biotechnology, vol. 20, no. 1, pp. 31-35, 2004.

[124] S. Repka, M. Van Der Vlies, and J. Vijverberg, "Food quality of detritus derived from the filamentous cyanobacterium Oscilatoria limnetica for Daphnia galeata," Journal of Plankton Research, vol. 20, no. 11, pp. 2199-2205, 1998.

[125] Y. Singh and H. D. Kumar, "Lipid and hydrocarbon production by Botryococcus spp. under nitrogen limitation and anaerobiosis," World Journal of Microbiology & Biotechnology, vol. 8, no. 2, pp. 121-124, 1992.

[126] L. Rodolfi, G. C. Zittelli, N. Bassi et al., "Microalgae for oil: strain selection, induction oflipid synthesis and outdoor mass cultivation in a low-cost photobioreactor," Biotechnology and Bioengineering, vol. 102, no. 1, pp. 100-112, 2009.

[127] J. R. Dean, Extraction Methods for Environmental Analysis, John Wiley & Sons, Chichester, UK, 1998.

[128] R. L. Mendes, H. L. Fernandes, J. P. Coelho et al., "Supercritical CO2 extraction of carotenoids and other lipids from Chlorella vulgaris," Food Chemistry, vol. 53, no. 1, pp. 99103, 1995.

[129] G. Andrich, U. Nesti, F. Venturi, A. Zinnai, and R. Fiorentini, "Supercritical fluid extraction of bioactive lipids from the microalga Nannochloropsis sp," European Journal of Lipid Science and Technology, vol. 107, no. 6, pp. 381-386, 2005.

[130] G. Andrich, A. Zinnai, U. Nesti, F. Venturi, and R. Fiorentini, "Supercritical fluid extraction of oil from microalga Spirulina

(Arthrospira) platensis," Acta Alimentaria, vol. 35, no. 2, pp. 195-203, 2006.

[131] R. Halim, B. Gladman, M. K. Danquah, and P. A. Webley, "Oil extraction from microalgae for biodiesel production," Bioresource Technology, vol. 102, no. 1, pp. 178-185, 2011.

[132] R. L. Mendes, B. P. Nobre, M. T. Cardoso, A. P. Pereira, and A. F. Palavra, "Supercritical carbon dioxide extraction of compounds with pharmaceutical importance from microalgae," Inorganica Chimica Acta, vol. 356, pp. 328-334, 2003.

[133] P. Spolaore, C. Joannis-Cassan, E. Duran, and A. Isambert, "Commercial applications of microalgae," Journal of Bioscience and Bioengineering, vol. 101, no. 2, pp. 87-96, 2006.

[134] K. Vijayaraghavan and K. Hemanathan, "Biodiesel production from freshwater algae," Energy & Fuels, vol. 23, no. 11, pp. 5448-5453, 2009.

[135] X. Meng, J. Yang, X. Xu, L. Zhang, Q. Nie, and M. Xian, "Biodiesel production from oleaginous microorganisms," Renewable Energy, vol. 34, no. 1, pp. 1-5, 2009.

[136] Q. Hu, M. Sommerfeld, E. Jarvis et al., "Microalgal triacyl-glycerols as feedstocks for biofuel production: perspectives and advances," Plant Journal, vol. 54, no. 4, pp. 621-639, 2008.

[137] G. Huang, F. Chen, D.Wei,X.Zhang,andG.Chen, "Biodiesel production by microalgal biotechnology," Applied Energy, vol. 87, no. 1, pp. 38-46, 2010.

[138] S. N. Naik, V. V. Goud, P. K. Rout, and A. K. Dalai, "Production of first and second generation biofuels: a comprehensive review," Renewable and Sustainable Energy Reviews, vol. 14, no. 2, pp. 578-597, 2010.

[139] S. A. Khan, Rashmi, M. Z. Hussain, S. Prasad, and U. C. Banerjee, "Prospects of biodiesel production from microalgae in India," Renewable and Sustainable Energy Reviews, vol. 13, no. 9, pp. 2361-2372, 2009.

[140] J. Knauer and P. C. Southgate, "A review of the nutritional requirements of bivalves and the development of alternative and artificial diets for bivalve aquaculture," Reviews in Fisheries Science, vol. 7, no. 3-4, pp. 241-280, 1999.

[141] E. W. Becker, "Micro-algae as a source of protein," Biotechnology Advances, vol. 25, no. 2, pp. 207-210, 2007.

[142] J. L. Harwood and I. A. Guschina, "The versatility of algae and their lipid metabolism," Biochimie, vol. 91, no. 6, pp. 679-684, 2009.

[143] C. M. Beal, C. H. Smith, M. E. Webber, R. S. Ruoff, and R. E. Hebner, "A framework to report the production of renewable diesel from algae," Bioenergy Research, vol. 4, no. 1, pp. 36-60, 2011.

[144] M. Gavrilescu and Y. Chisti, "Biotechnology—a sustainable alternative for chemical industry," Biotechnology Advances, vol. 23, no. 7-8, pp. 471-499, 2005.

[145] P. G. Roessler et al., "Genetic-engineering approaches for enhanced production of biodiesel fuel from microalgae," in ACS Symposium Series, pp. 255-270, 1994.

[146] J. Singh and S. Gu, "Commercialization potential of microalgae for biofuels production," Renewable and Sustainable Energy Reviews, vol. 14, pp. 2596-2610, 2010.

[147] M. Aresta, A. Dibenedetto, M. Carone, T. Colonna, and C. Fragale, "Production of biodiesel from macroalgae by supercritical CO2 extraction and thermochemical liquefaction," Environmental Chemistry Letters, vol. 3, no. 3, pp. 136-139, 2005.

[148] K. G. Satyanarayana, A. B. Mariano, and J. V. C. Vargas, "A review on microalgae, a versatile source for sustainable energy and materials," International Journal of Energy Research, vol. 35, no. 4, pp. 291-311, 2011.

[149] J. Singh and S. Gu, "Commercialization potential of microalgae for biofuels production," Renewable and Sustainable Energy Reviews, vol. 14, no. 9, pp. X2596-2610, 2010.

[150] H. C. Greenwell, L. M. L. Laurens, R. J. Shields, R. W. Lovitt, and K. J. Flynn, "Placing microalgae on the biofuels priority list: a review of the technological challenges," Journal of the Royal Society Interface, vol. 7, no. 46, pp. 703-726, 2010.

[151] T. M. Mata, A. A. Martins, and N. S. Caetano, "Microalgae for biodiesel production and other applications: a review," Renewable and Sustainable Energy Reviews, vol. 14, no. 1, pp. 217-232,2010.

[152] L. M. Brown and K. G. Zeiler, "Aquatic biomass and carbon dioxide trapping," Energy Conversion and Management, vol. 34, no. 9-11, pp. 1005-1013, 1993.

[153] P. Schenk et al., "Second generation biofuels: high-efficiency microalgae for biodiesel production," BioEnergy Research, vol. 1, no. 1, pp. 20-43, 2008.

[154] X. Li, H. Xu, and Q. Wu, "Large-scale biodiesel production from microalga Chlorella protothecoides through heterotrophic cultivation in bioreactors," Biotechnology and Bioengineering, vol. 98, no. 4, pp. 764-771, 2007.

[155] Y. Cheng, W. Zhou, C. Gao, K. Lan, Y. Gao, and Q. Wu, "Biodiesel production from Jerusalem artichoke (Helianthus Tuberosus L.) tuber by heterotrophic microalgae Chlorella protothecoides," Journal of Chemical Technology & Biotechnology, vol. 84, no. 5, pp. 777-781, 2009.

[156] Y. Lu, Y. Zhai, M. Liu, and Q. Wu, "Biodiesel production from algal oil using cassava (Manihot esculenta Crantz) as feedstock," Journal of Applied Phycology, vol. 22, no. 5, pp. 573-578,2010.

[157] P. T. Vasudevan and M. Briggs, "Biodiesel production— current state of the art and challenges," Journal of Industrial Microbiology & Biotechnology, vol. 35, no. 5, pp. 421-430, 2008.

[158] A. H. Scragg, Biofuels, Production, Application and Development, Cambridge University Press, Cambridge, UK, 2009.

[159] R. A. Holser and R. Harry-O'Kuru, "Transesterified milkweed (Asclepias) seed oil as a biodiesel fuel," Fuel, vol. 85, no. 14-15, pp. 2106-2110,2006.

[160] N. A. Santos, J. R. J. Santos, F. S. M. Sinfronio et al., "Thermo-oxidative stability and cold flow properties of babassu biodiesel by PDSC and TMDSC techniques," Journal of Thermal Analysis and Calorimetry, vol. 97, no. 2, pp. 611614, 2009.

[161] A. Richmond, "Open systems for the mass production of photoautotrophic microalgae outdoors: physiological principles," Journal of Applied Phycology, vol. 4, no. 3, pp. 281-286, 1992.

[162] R. Harun, M. Singh, G. M. Forde, and M. K. Danquah, "Bioprocess engineering of microalgae to produce a variety of consumer products," Renewable and Sustainable Energy Reviews, vol. 14, no. 3, pp. 1037-1047, 2010.

[163] M. R. Tredici and R. Materassi, "From open ponds to vertical alveolar panels: the Italian experience in the development of reactors for the mass cultivation of phototrophic microorganisms," Journal of Applied Phycology, vol. 4, no. 3, pp. 221231, 1992.

[164] D. Chaumont, "Biotechnology of algal biomass production: a review of systems for outdoor mass culture," Journal of Applied Phycology, vol. 5, no. 6, pp. 593-604, 1993.

[165] O. R. Zaborsky et al., "An automated helical photobioreactor incorporating cyanobacteria for continuous hydrogen production," in BioHydrogen, pp. 431-440, Springer, New York, NY, USA, 1999.

[166] P. T. Vasudevan and B. Fu, "Environmentally sustainable biofuels: advances in biodiesel research," Waste and Biomass Valorization, pp. 1-17, 2010.

[167] M. E. Huntley and D. G. Redalje, "CO2 mitigation and renewable oil from photosynthetic microbes: a new appraisal," Mitigation and Adaptation Strategies for Global Change, vol. 12, no. 4, pp. 573-608, 2007.

[168] A. M. Illman, A. H. Scragg, and S. W. Shales, "Increase in Chlorella strains calorific values when grown in low nitrogen medium," Enzyme and Microbial Technology, vol. 27, no. 8, pp. 631-635, 2000.

[169] A. H. Scragg, A. M. Illman, A. Carden, and S. W. Shales, "Growth of microalgae with increased calorific values in a tubular bioreactor," Biomass and Bioenergy, vol. 23, no. 1, pp. 67-73, 2002.

[170] A. Widjaja, C. C. Chien, and Y. H. Ju, "Study of increasing lipid production from fresh water microalgae Chlorella vul-garis," Journal of the Taiwan Institute of Chemical Engineers, vol. 40, no. 1, pp. 13-20, 2009.

[171] S.-Y. Chiu, C. Y. Kao, M. T. Tsai, S. C. Ong, C. H. Chen, and C. S. Lin, "Lipid accumulation and CO2 utilization of Nannochloropsis oculata in response to CO2 aeration," Bioresource Technology, vol. 100, no. 2, pp. 833-838, 2009.

[172] H. Tang et al., "Potential of microalgae oil from Dunaliella tertiolecta as a feedstock for biodiesel," Applied Energy, vol. 88, no. 10, pp. 3324-3330, 2011.

[173] W. R. Barclay, K. M. Meager, and J. R. Abril, "Heterotrophic production of long chain omega-3 fatty acids utilizing algae and algae-like microorganisms," Journal of Applied Phycology, vol. 6, no. 2, pp. 123-129, 1994.

[174] Y. Liang, N. Sarkany, and Y. Cui, "Biomass and lipid productivities of Chlorella vulgaris under autotrophic, heterotrophic and mixotrophic growth conditions," Biotechnology Letters, vol. 31, no. 7, pp. 1043-1049, 2009.

[175] K. Muffler and R. Ulber, "Downstream processing in marine biotechnology," in Marine Biotechnology II, Y. L. Gal and R. Ulber, Eds., p. 261, Springer, New York, NY, USA, 1st edition, 2005.

[176] J. O'Grady and J. A. Morgan, "Heterotrophic growth and lipid production of Chlorella protothecoides on glycerol," Bioprocess and Biosystems Engineering, vol. 34, no. 1, pp. 121125,2011.

[177] H. Xu, X. Miao, and Q. Wu, "High quality biodiesel production from a microalga Chlorella protothecoides by heterotrophic growth in fermenters," Journal of Biotechnology, vol. 126, no. 4, pp. 499-507, 2006.

[178] J. Liu, J. Huang, Z. Sun, Y. Zhong, Y. Jiang, and F. Chen, "Differential lipid and fatty acid profiles of photoautotrophic and heterotrophic Chlorella zofingiensis: assessment of algal oils for biodiesel production," Bioresource Technology, vol. 102, no. 1,pp. 106-110,2011.

[179] L. E. Dong, K. J. Drury, and A. G. Fadeev, "Methods for Harvesting Biological Materials Using Membrane Filters," US Patent 20100184197, 2010.

[180] A. Lamers, "Algae oils from small scale low input water remediation site as feedstock for biodiesel conversion," Guelph EngineeringJournal, vol. 2, pp. 24-38, 2009.

[181] Y. Li, M. Horsman, N. Wu, C. Q. Lan, andN. Dubois-Calero, "Biofuels from microalgae," Biotechnology Progress, vol. 24, no. 4, pp. 815-820, 2008.

[182] M. K. Danquah, L. Ang, N. Uduman, N. Moheimani, and G. M. Forde, "Dewatering of microalgal culture for biodiesel

production: exploring polymer flocculation and tangential flow filtration," Journal of Chemical Technology & Biotechnology, vol. 84, no. 7, pp. 1078-1083, 2009.

[183] N. Uduman et al., "Dewatering of microalgal cultures: a major bottleneck to algae-based fuels," Journal of Renewable Sustainable Energy, vol. 2, p. 012701, 2010.

[184] E. Molina Grima, E. H. Belarbi, F. G. Acien Fernández, A. Robles Medina, and Y. Chisti, "Recovery of microalgal biomass and metabolites: process options and economics," Biotechnology Advances, vol. 20, no. 7-8, pp. 491-515, 2003.

[185] C. Gudin and C. Therpenier, "Bioconversion of solar energy into organic chemicals by microalgae," Advanced Biotechnology Processes, vol. 6, pp. 73-110, 1986.

[186] M. Olaizola, "Commercial development of microalgal biotechnology: from the test tube to the marketplace," Biomolecular Engineering, vol. 20, no. 4-6, pp. 459-466, 2003.

[187] H. M. Oh, S. J. Lee, M. H. Park et al., "Harvesting of Chlorella vulgaris using a bioflocculant from Paenibacillus sp. AM49," Biotechnology Letters, vol. 23, no. 15, pp. 1229-1234, 2001.

[188] M. W. Tenney et al., "Algal flocculation with synthetic organic polyelectrolytes," Applied and Environmental Microbiology, vol. 18, no. 6, pp. 965-971, 1969.

[189] G. Shelef, A. Sukenik, and M. Green, "Microalgae harvesting and processing: a literature review," Tech. Rep., Technion Research and Development, 1984.

[190] G. Ahlgren and L. Merino, "Lipid analysis of freshwater microalgae : a method study," Archiv fur Hydrobiologie, vol. 121, no. 3, pp. 295-306, 1991.

[191] E. H. Belarbi, E. Molina, and Y. Chisti, "A process for high yield and scaleable recovery of high purity eicosapentaenoic acid esters from microalgae and fish oil," Process Biochemistry, vol. 35, no. 9, pp. 951-969, 2000.

[192] E. M. Grima, A. R. Medina, A. G. Gimenez, J. A. Sanchez Perez, F. G. Camacho, and J. L. García Sánchez, "Comparison between extraction of lipids and fatty acids from microalgal biomass," Journal of the American Oil Chemists' Society, vol. 71, no. 9, pp. 955-959, 1994.

[193] A. R. Fajardo, L. E. Cerdan, A. R. Medina, F. G. A. Fernandez, P. A. G. Moreno, and E. M. Grima, "Lipid extraction from the microalga Phaeodactylum tricornutum," European Journal of Lipid Science and Technology, vol. 109, no. 2, pp. 120-126, 2007.

[194] C. Y. Chen, K. L. Yeh, H. M. Su, Y. C. Lo, W. M. Chen, and J. S. Chang, "Strategies to enhance cell growth and achieve high-level oil production of a Chlorella vulgaris isolate," Biotechnology Progress, vol. 26, no. 3, pp. 679-686, 2010.

[195] A. Morist, J. L. Montesinos, J. A. Cusido, and F. Godia, "Recovery and treatment ofSpirulina platensis cells cultured in a continuous photobioreactor to be used as food," Process Biochemistry, vol. 37, no. 5, pp. 535-547, 2001.

[196] E. A. Ehimen et al., "Energy recovery from lipid extracted, transesterified and glycerol codigested microalgae biomass," GCB Bioenergy, vol. 1, no. 6, pp. 371-381, 2009.

[197] Y. Chisti and M. Moo-Young, "Disruption of microbial cells for intracellular products," Enzyme and Microbial Technology, vol. 8, no. 4, pp. 194-204, 1986.

[198] M. Ottens, J. A. Wesselingh, and L. A. M. V. D. Wielen, "Downstream processing," in Basic Biotechnology, C. Ratledge and B. Kristiansen, Eds., p. 666, Cambridge University Press, New York, NY, USA, 3rd edition, 2006.

[199] C. L. Peterson, D. L. Auld, and R. A. Korus, "Winter rape oil fuel for diesel engines: recovery and utilization," Journal of the American Oil Chemists' Society, vol. 60, no. 8, pp. 1579-1587, 1983.

[200] Z. Khan, J. Troquet, and C. Vachelard, "Sample preparation and analytical techniques for determination of polyaromatic hydrocarbons in soils," International Journal of Environmental Science and Technology, vol. 2, no. 3, pp. 275-286, 2005.

[201] E. G. Bligh and W. J. Dyer, "A rapid method of total lipid extraction and purification," Canadian Journal of Biochemistry and Physiology, vol. 37, no. 8, pp. 911-917, 1959.

[202] S. Lee, B.-D. Yoon, and H.-. Oh, "Rapid method for the determination of lipid from the green alga Botryococcus braunii," Biotechnology Techniques, vol. 12, no. 7, pp. 553556, 1998.

[203] N. Nagle and P. Lemke, "Production of methyl ester fuel from microalgae," Applied Biochemistry and Biotechnology, vol. 2425, pp. 355-361, 1990.

[204] L. Govindarajan, N. Raut, and A. Alsaeed, "Novel solvent extraction for extraction of oil from algae biomass growth in desalination reject stream," Journal of Algal Biomass Utilization, vol. 1, no. 1, pp. 18-28, 2009.

[205] M. Herrero, A. Cifuentes, and E. Ibanez, "Sub- and supercritical fluid extraction of functional ingredients from different natural sources: plants, food-by-products, algae and microalgae—a review," Food Chemistry, vol. 98, no. 1, pp. 136-148, 2006.

[206] M. Bender, "Economic feasibility review for community-scale farmer cooperatives for biodiesel," Bioresource Technology, vol. 70, no. 1, pp. 81-87, 1999.

[207] C. Manivannan and S. P. Sawan, "The supercritical state," in Supercritical Fluid Cleaning: Fundamentals, Technology, and Applications, pp. 1-2, William Andrew, 1998.

[208] Z. Berk, Food Process Engineering and Technology, Elsevier, New York, NY, USA, 2009.

[209] G. Brunner, "Supercritical fluids: technology and application to food processing," Journal of Food Engineering, vol. 67, no. 1-2, pp. 21-33, 2005.

[210] H. Berg, M. Mágard, G. Johansson, and L. Mathiasson, "Development of a supercritical fluid extraction method for determination of lipid classes and total fat in meats and its comparison with conventional methods," Journal of Chromatography A, vol. 785, no. 1-2, pp. 345-352, 1997.

[211] H. Saad and E. Gulari, "Diffusion of liquid hydrocarbons in supercritical CO2 by photon correlation spectroscopy," BerichtederBunsen-GesellschaftfurPhysikalische Chemie, vol. 88, no. 9, pp. 834-837, 1984.

[212] J. P. Friedrich and E. H. Pryde, "Supercritical CO2 extraction of lipid-bearing materials and characterization of the products," Journal of the American Oil Chemists' Society, vol. 61, no. 2, pp. 223-228, 1984.

[213] P. Tonthubthimthong, P. L. Douglas, S. Douglas, W. Luewisutthichat, W. Teppaitoon, and L. E. Pengsopa, "Extraction of nimbin from neem seeds using supercritical CO2 and a supercritical CO2-methanol mixture," Journal of Supercritical Fluids, vol. 30, no. 3, pp. 287-301, 2004.

[214] W. E. Brewer, R. C. Galipo, K. W. Sellers, and S. L. Morgan, "Analysis of cocaine, benzoylecgonine, codeine, and morphine in hair by supercritical fluid extraction with carbon dioxide modified with methanol," Analytical Chemistry, vol. 73, no. 11, pp. 2371-2376, 2001.

[215] N. Aghel, Y. Yamini, A. Hadjiakhoondi, and S. M. Pourmor-tazavi, "Supercritical carbon dioxide extraction of Mentha pulegium L. essential oil," Talanta, vol. 62, no. 2, pp. 407411,2004.

[216] R. M. Couto, P. C. Simoes, A. Reis, T. L. Da Silva, V. H. Martins, and Y. Sánchez-Vicente, "Supercritical fluid extraction of lipids from the heterotrophic microalga Crypthecodinium

cohnii," Engineering in Life Sciences, vol. 10, no. 2, pp. 158164, 2010.

[217] R. L. Mendes, A. D. Reis, and A. F. Palavra, "Supercritical CO2 extraction of y-linolenic acid and other lipids from Arthrospira (Spirulina)maxima: comparison with organic solvent extraction," Food Chemistry, vol. 99, no. 1, pp. 57-63, 2006.

[218] C. G. Laudani, M. Habulin, Z. Knez, G. D. Porta, and E. Reverchon, "Lipase-catalyzed long chain fatty ester synthesis in dense carbon dioxide: kinetics and thermodynamics," Journal of Supercritical Fluids, vol. 41, no. 1, pp. 92-101,2007.

[219] D. Oliveira and J. V. Oliveira, "Enzymatic alcoholysis ofpalm kernel oil in n-hexane and SCCO2" Journal of Supercritical Fluids, vol. 19, no. 2, pp. 141-148, 2001.

[220] M. N. Varma and G. Madras, "Synthesis of biodiesel from castor oil and linseed oil in supercritical fluids," Industrial and Engineering Chemistry Research, vol. 46, no. 1, pp. 1-6, 2007.

[221] M. N. Varma, P. A. Deshpande, and G. Madras, "Synthesis ofbiodiesel in supercritical alcohols and supercritical carbon dioxide," Fuel, vol. 89, no. 7, pp. 1641-1646, 2010.

[222] A. Carrero et al., "Hierarchical zeolites as catalysts for biodiesel production from Nannochloropsis microalga oil," Catalysis Today, vol. 167, no. 1, pp. 148-153, 2011.

[223] E. A. Ehimen, Z. F. Sun, and C. G. Carrington, "Variables affecting the in situ transesterification of microalgae lipids," Fuel, vol. 89, no. 3, pp. 677-684, 2010.

[224] B. D. Wahlen, R. M. Willis, and L. C. Seefeldt, "Biodiesel production by simultaneous extraction and conversion of total lipids from microalgae, cyanobacteria, and wild mixed-cultures," Bioresource Technology, vol. 102, no. 3, pp. 27242730, 2011.

[225] W. Xiong, X. Li, J. Xiang, and Q. Wu, "High-density fermentation of microalga Chlorella protothecoides in bioreactor for microbio-diesel production," Applied Microbiology and Biotechnology, vol. 78, no. 1, pp. 29-36, 2008.

[226] M. Lanza, W. L. Priamo, J. V. Oliveira, C. Dariva, and D. De Oliveira, "The effect of temperature, pressure, exposure time, and depressurization rate on lipase activity in SCCO2," Applied Biochemistry and Biotechnology Part A, vol. 113, no. 1-3, pp. 181-187, 2004.

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