Mayor producer for several vegetable oils (O’Brien et al., 2000).
Biodiesel is a renewable liquid biofuel produced from renewable lipid sources such as vegetable oils or animal fats. It results from the transesterification reaction of triglycerides with an alcohol in the presence of a catalyst; see Figure 1 (Marchetti et al., 2007, Srivastava & Prasad, 2000, Ma & Hanna, 1999).
The transesterification reaction is a series of reactions where from triglycerides diglycerides are produced, from these ones monoglycerides are produced and finally, from these monoglycerides glycerol is produced. In all these steps, fatty acid alkyl ester (biodiesel) is formed.
This reaction is most commonly catalyzed by a homogeneous base catalyst that could be sodium hydroxide among others. However, to be able to use this type of catalyst, the raw material needed is a refined vegetable oil. If more impure oil is used together with some free fatty acids and sodium hydroxide in it, the fatty acid involved in the saponification reaction will consume the catalyst. The soap produced will also be a problem for the downstreaming separation of the biodiesel and the glycerol. The saponification reaction could be seen in Figure 2 (Marchetti et al., 2007, Srivastava & Prasad, 2000, Ma & Hanna, 1999, Fukuda et al., 2001, Knothe et al., 2005, Marchetti, 2010).
In order to avoid this problem, the technological solutions put forward were: the use of homogeneous acidic catalysts such as sulfuric acid (Knothe et al., 2005, Marchetti, 2010, Schuchardt et al., 1998, Noureddini & Zhu, 1997, Freedman et al., 1984, Zheng et al., 2006, Canakci & Van Gerpen, 2003a, 2003b), solid catalysts such as zeolites, solid resins (basic as well as acid) (Bournay et al., 2005, Di Serio et al., 2005, 2006, Soriano et al., 2009, Hamad et al., 2008, Suppes et al., 2004, Kulkarni et al., 2006, López et al., 2008, Cao et al, 2008), enzymatic technologies (Bajaj et al., 2010, Ranganathan et al., 2008, Antczak et al, 2009, Rodrigues et al., 2008, Dalla Rosa et al., 2008, Matassoli et al., 2008), supercritical alcohols (Demirbaş, 2002, 2003, Saka & Kusdiana, 2001, Kusdiana & Saka, 2001, 2004, Hawash et al., 2009, Gui et al., 2008, Kasim et al. 2009), membrane reactors (Dubé et al. 2007, Baroutian et al., 2011, Zhu et al., 2010, Cheng et al., 2010, Cao et al., 2008), monolithic reactors (Kolaczkowski et al., 2009, Dizge et al., 2009, Tonetto & Marchetti, 2010), etc.
All these technological solutions have many advantages over each other but also some drawbacks due to different considerations; for instance, reaction time, reaction temperature, operational cost, amount of equipment, quality of the final product, complexity of purification, and so forth (Srivastava & Prasad, 2000, Ma & Hanna, 1999,Marchetti, 2010, Schuchardt et al., 1998).
Furthermore, all these new technologies have a real advantage: they can be used for treating less pure raw materials, allowing a higher presence of free fatty acids and, in some cases, the presence of water. This is pertinent not only to the increasing Food vs. Fuel debate, but also to the one about how the vegetable oil we produce should be used. By applying these technologies, typical pollutants can be consumed, and crude oil, waste, as well as frying oil, soapstocks, and the like, can be used as raw materials for Biodiesel production. As a result, all the refined oil could be left for human consumption.
There is a need of knowing more about the different biodiesel technologies based on the type of raw materials they are able to treat. This work aims to shed light on the subject by presenting a comparison of the different qualities of vegetable oils, comparing the physical-chemical properties of these oils, and their influences over the final biofuel.
2. Global situation of the vegetable oil market
Since the beginning of the 19th century, people have used vegetable oils and animal fats based on the knowledge storage over centuries and not so much on the scientific knowledge as it are today; based on their structure, physical properties, etc. The need of understanding and knowing more about the vegetable oil arises due to the increasing value of this product as for example in its use in medicine, cosmetics as well as for fuel for lighting.
Normally, vegetable oils are obtained from different plants seeds, such as sunflower, peanut, coconut, palm, palm kernel, soybean, corn, and many other options. To chose from which of these vegetables produce the oil depends on several factors, some of them are the location of the landscape, the climate of the region, the nutrients of the soil as many other environmental as well as economic variables (it is also important which oil has a better market to be sold). Based on some types of seeds, O´Brien et al. 2000, have done a compilation showing where some of the main seeds are being cultivate around the world. An extraction from their work it could be seen in Table 1.
|Seed||Amount of oil (%)||Productive areas|
|Canola||40-45||Canada, China, India, France, Austria, United Kingdom, Germany, Poland, Denmark, Check Republic.|
|Corn||3.1-5.7||USA, Mexico, Russia, Belgium, France, Italy, Germany, Spain, United Kingdom.|
|Cotton||18-20||China, Russia, USA, India, Pakistan, Brazil, Egypt, Turkey.|
|Peanut||45-50||China, India, Nigeria, USA, Senegal, South Africa, Argentina|
|Crocus||30-35||China, USA, Spain, Portugal|
|Soybean||18-20||USA, Brazil, Argentina, China, India, Paraguay, Bolivia|
|Sunflower||35-45||Russia, Argentina, Austria, France, Italia, Germany, Spain, United Kingdom.|
|Coconut||65-68||Filipinas, Indonesia, India, México Sri Lanka, Thailand, Malaysia, Vietnam, Mozambique, New Guinea, Republic of Côte d'Ivoire|
|Olive||15-35||Spain, Italy, Italia, Greece, Tunes, Turkey, Morocco, Portugal, Syria, Algeria, Yugoslavia, Egypt, Israel, Libya, Jordan, Lebanon, Argentina, Chile, Mexico, Peru, USA, Australia.|
|Palm||45-50||Malaysia, Indonesia, China, Filipinas, Pakistan, México, Bangladesh, Colombia, Nigeria, Republic of Côte d'Ivoire|
|Palm kernel||44-53||Malaysia, Indonesia, China, Filipinas, Pakistan, México, Bangladesh, Colombia, Nigeria, Republic of Côte d'Ivoire|
In Table 1 it is presented the mayor regions where different oils are being produced as well as the percentage of oil in each seed. It could be seen that even when each seed produce different amounts of oil, there are several of them that produce an amount between 30 and 53 %.
Even more, the price of vegetable oil has become quite volatile over the last year (www.indexmundi.com (a)). In Figure 3 it can be seen the fluctuation of prices for soybean oil for the last 30 years (www.indexmundi.com (b)). In the case of soybean oil, there is a major peak in June 2008, (where the price of the soybean oil have reached values of 1414 US$)
The soybean oil situation is similar to that of the major oils such as sunflower, coconut, rapeseed, palm, palm kernel, olive, etc., being the case presented in Figure 3 just as an example. It is also important to notice that the evolution of the vegetable oil prices is link directly to the prices of petroleum oil. Figure 4 shows the evolution of the petroleum prices as well as the price of the soybean oil. When petroleum prices increases there is an increase in soybean oil; however, the increases in soybean oil are not only associated to petroleum crisis.
3. Vegetable oil: types and composition
Due to the different origin of the vegetable oils, their structure and composition vary from one to another, mainly in the length of the hydrocarbon chain, as well as in the amount and location of the double bonds. O’Brien et al., (O’Brien et al., 2000) have performed a comparison with some of the main types of oil and the percentage of the different types of fatty acids involves. Table 2, extracted from reference O’Brien et al., 2000 shows these percentages.
As it could be seen from Table 2, the main composition fatty acid compositions of the vegetable oils is generally based on a C18 carbon length, with one or two double bonds, this is the case for corn, cottonseed, peanut, rapeseed, soybean and sunflower. For crambe oil, the main contribution is by C22:1. However, the second and third most abundant fatty acid is different from oil to oil. It is important to point out that, even thought there are differences in the fatty acid composition of different oils, the major participations are always from carbon chain with double bonds
|Vegetable oil||Fatty acid composition % by weight|
The diverse composition of the different types of oil also affects their main physical-chemical properties due to the carbon length and the double bonds. Table 3 presents some major properties for 6 typical types of vegetable oil.
It could be seen that in some cases the properties values are quite similar; that is the case of the specific gravity and the smoke point. On the other hand the flash point is quite diverse, changing from 225 °C to 327°C. Another property that has a wider range is the acid value, going from 0.6 to 6.6 accordingly.
So far, it has been presented the properties of refine oils. However, as it will be point out later in this chapter, the need for a less pure raw material, and therefore cheaper, is imperative. The main possibilities are frying, waste, cooking oils, soapstocks as well as oil from algae and non edible oils. The first four options are considered waste. On the other hand, the oil from algae is not a waste but could be considered as non edible oil.
Table 3 shows some of the main properties of refined, crude and waste oil to compare the different types of oil. There, it is clear that the sulfur content increases considerably when comparing refined oil with waste oil. Similar results could be found when comparing the acid value.
On the other hand, the viscosity values do not change that much due to the presence of impurities.
Among the non edible oils, Table 4 shows the variation of some parameters for 4 types of non edible oils.
|Property||Refine [*]||Crude [+]||Waste [x]|
|Kinematics viscosity [mm2/s]||30.2||36||40.2|
|Carbon residue [wt%.]||0.24||0.278||0.18|
|Higher heating value [MJ/kg]||39.41||39.2||24.67|
|Ash content [wt%]||0.012||0.01||---|
|Sulfur content [wt%]||0.013||0.075||5|
|Iodine value [centigram I/g Oil]||112.86||125||13.2|
|Acid value [mg KOH/g Oil]||<0.2||variable||5.96|
|Parameters||Non Edible Oils|
|Calorific value [MJ/kg]||39.23||36.50||39.5||---|
|Flash point [°C]||135||130||260||150|
|Cloud point [°C]||---||4||-12||---|
|Pour point [°C]||2||---||-32||---|
|Ash content [wt%]||0.012||…||0.020||0.0005|
|Acid value [mg KOH/g]||0.400||0.118||---||0.620|
Gradually, a third type of oil is bearing relevance due to a number of advantages. This third type is produced from algae. Algae are microscopic organisms which could be used for the production of different types of fuel such as biodiesel, bio-hydrogen production, methane, etc. Algae have several advantages to be used for producing biofuel, some of them are:
they required CO2 to grow,
they grow in non drinkable water, not competing with drinkable sources,
algae could grow in land fields where no other vegetable oil could grow,
algae could be use as raw materials for several other chemical compounds easy to produce.
It could be seen that this percentage varies from 15 to over 75 % being the last quite suitable for producing the oil to be use in the production of biofuels.
|Microalgae||Oil content (% dry wt.)|
Mata et al. (Mata et al., 2010) have done a research on how much biodiesel could be produce by growing different seeds in one ha. They work shows that, among those sources studied; corn has the lowest one production rate per year in 1 hectare (151 kg of biodiesel); sunflower oil is place in middle position with a production close to 1000 kilos per year per hectare; while microalgae are place quite high above. In regard to microalgae, they are classified depending on their oil content, which is divided into low, medium and high. The result is a production of 51.297, 86.515 and 121.104 kilos of biodiesel per year and per hectare respectively. This shows algae as an interesting new alternative source of vegetable oil for biodiesel.
So far it has been presented the difference in the vegetable oil accordingly to the quality of them as well as to be from different seeds, also it was presented a comparison among non edible oil and oil from algae. Thus, when comparing biodiesel from different sources, the nature of the vegetable oil is to be considered because of its effect over some of the major physical and chemical.
As it could be seen from Table 6 (Moser, 2009), when comparing the methyl esters from fatty acid with no double bonds, the increase in the chain length produce a higher viscosity. However, when double bonds are being considered, the viscosity tend to decrease as long as the amount of double bonds increases, this could be seen for C18:0 ME, C18:1 ME, C18:2 ME and 18:3 ME. When looking into the type of alcohol used, the longer the alcohol chain is the higher the viscosity of the biodiesel.
A similar scenario could be seen when comparing the cetane number, when the carbon chain or the alcohol chain increases, the cetane number increases as well, however, the presence of double bonds will decrease this property considerably.
|FAEE||Melting point (°C)||ΔcH (MJ/mol)||Kinematics viscosity (mm2/s)||Oil stability index (h)||Cetane Number||Lub (μm)|
4. Some about biodiesel production
So far, it has been considered the different raw materials and the different types of oil quality. It is important to describe some of the fundamentals of biodiesel production before reflecting on selecting the appropriate technology to use. In section 5, it will be presented different technologies and how the quality of the raw material might have an effect or might be a key factor on the decision of which production alternative should be use, and which should be avoid.
Biodiesel is a renewable and alternative liquid biofuel normally produce from vegetable oils or animal fats by the transesterification reaction (see Figure 1). Not any fuel produced from vegetable oils can be called biodiesel. Therefore, there are international standards to be reached, these are, ASTM D7467, EN 14214. The European Standard EN 14214 could be seen in Table 7 (
The transesterification reaction, when carried on with a basic homogeneous catalyst, sodium or potassium hydroxide or methoxide (Marchetti et al., 2007, Srivastava & Prasad, 2000, Ma & Hanna, 1999, Fukuda et al., 2001, Knothe et al., 2005, Marchetti, 2010, Vicente et al., 2004, Meng et al., 2008, Alamu et al., 2007, Dias et al., 2008), has shown great potential producing the fuel under specification in around two hours (Srivastava & Prasad, 2000, Ma & Hanna, 1999, Fukuda et al., 2001, Knothe et al., 2005, Marchetti, 2010).
The major drawback of this technology is the need of refined oil which is on the hot spot due to the Fuel vs. Food debate. Due to the need of oil for feeding purposes and for biofuel production; alternative raw materials, pointed out in section 2, are being evaluated, tested and used. The uses of these new raw materials have generated new processes to carry on the transesterification reaction, example of this are: acid homogeneous catalyst (Marchetti et al., 2007, Srivastava & Prasad, 2000, Ma & Hanna, 1999, Fukuda et al., 2001, Knothe et al., 2005, Marchetti, 2010, Zheng et al., 2006, Canakci & Van Gerpen, 2003 a,b), solid resins (Bajaj et al., 2010, Ranganathan et al., 2008, Antczak et al, 2009, Rodrigues et al., 2008, Dalla Rosa et al., 2008, Matassoli et al., 2008),supercritical alcohols (Demirbaş, 2002, 2003, Saka & Kusdiana, 2001, Kusdiana & Saka, 2001, 2004, Hawash et al., 2009, Gui et al., 2008, Kasim et al. 2009),
|Esters amount||% (mol/mol)||96.5||EN 14103|
|Density at 15°C||kg/m3||860-900||EN ISO 3675,|
EN ISO 12185
|Kinematics Viscosity at 40°C||mm2/s||3.5-||EN ISO 3104,|
|Flash Point||°C||120 min||EN ISO 3679|
|Sulfur content||mg/kg||10.0 max||EN ISO 20846,|
EN ISO 20884
|Carbon residue||% (mol/mol)||0.3 max||EN ISO 10370|
|Cetane Number||51 min||EN ISO 5165|
|Sulfated ash||% (mol/mol)||0.02 max||ISO 3987|
|Water content||mg/kg||500 max||EN ISO 12937|
|Total Contamination||mg/kg||24 max||EN 12662|
|Copper strip corrosion (3 h, 50°C)||Degree of corrosion||1||EN ISO 2160|
|Oxidation stability, 110C||H||6.0 min||EN 14112|
|Acid number||mg KOH/g||0.50 max||EN 14104|
|Iodo number||g I2/100 g||120 max||EN 14111|
|Linolenic acid content||% (mol/mol)||12.0 max||EN 14103|
|Polyunsaturated methyl ester||% (mol/mol)||1 max||EN 14103|
|Methanol content||% (mol/mol)||0.2 max||EN 14110|
|MAG content||% (mol/mol)||0.8 max||EN 14105|
|DAG content||% (mol/mol)||0.2 max||EN 14105|
|TAG content||% (mol/mol)||0.2 max||EN 14105|
|Free Glycerol||% (mol/mol)||0.02max||EN 14105, EN 14106|
|Total Glycerol||% (mol/mol)||0.25 max||EN 14105|
|Group I metals||mg/kg||5.0 max||EN 14108, EN 14109|
|Group II metal||mg/kg||5.0 max||EN 14538|
|Phosphorous content||mg/kg||10.0 max||EN 14107|
membrane reactors (Dubé et al. 2007, Baroutian et al., 2011, Zhu et al., 2010, Cheng et al., 2010, Cao et al., 2008), monolithic catalysts (Kolaczkowski et al., 2009, Dizge et al., 2009, Tonetto & Marchetti, 2010), etc.
Besides the different technologies and their applicability, we would like to introduce a few thoughts in relation to the prospective future of biodiesel production. Johnston & Holloway (Johnston & Holloway, 2007) have compared 228 countries comparing their potential production of biodiesel. According to them, the five countries with the absolute biodiesel potential are Malaysia, Indonesia, Argentina, USA and Brazil. However, when considering the high potential of production in combination with the low production cost, the top five countries are Malaysia, Indonesia, Philippines, Papua New Guinea, and Thailand. This result is relevant to draw the attention to new possible production markets.
5. A comparison of the different production technologies
As mentioned before, many works have been carried on in order to find new alternative technologies to produce biodiesel from impure raw material such as crude oil, waste or cooking oil, frying oil, soapstoacks’, animal fat, etc. In a typical biodiesel production flow diagram (Figure 5), a few equipments might not be needed for all the technologies available. However, to show the most general case, we have added separation and purification processes as a rule. In some cases, purification is not required, and in some other a pre-esterification before the transesterification reaction is needed. A more complete flow
When using a homogeneous acid catalyst, like sulfuric acid, the transesterification reaction is 4000 times slower (Srivastava & Prasad, 2000, Ma & Hanna, 1999, Fukuda et al., 2001, Knothe et al., 2005, Marchetti, 2010), compared with when a base homogeneous catalyst is used. Nevertheless, the esterification reaction could also take place and be carried on without generating soaps. Therefore, this catalyst allows to treat less pure raw material with some fatty acids and/or water within it (Canakci & Van Gerpen, 2003 a,b, Marchetti & Errazu, 2008).
On the other hand, since the catalyst is in homogeneous phase, the need of neutralization, purification, and separation, are required. As a consequences, effluents as well as non desirable by-products result; this increases the amount of energy and equipments required. Thus, a bigger initial investment is needed. Finally, it is obtained a Biodiesel of good quality and a by-product, glycerin, which is of industrial grade allowing it to be used for other purposes or to be purified until pharmaceutical grade (Van Gerpen, 2005, Marchetti & Errazu, 2008).
In order to avoid some of the neutralization and purification equipments, the use of a heterogeneous catalyst appears to be a good brand new alternative. In this case, solid acid resins and basic solid resins could be used obtaining good results (Bournay et al., 2005, Di Serio et al., 2005, 2006, Soriano et al., 2009, Hamad et al., 2008, Suppes et al., 2004, Kulkarni et al., 2006, López et al., 2008, Cao et al, 2008). The advantages of using this catalyst appears in the final products obtained, more pure Biodiesel and glycerin;: and also, in the process itself, which required less equipment and ergo a lower investment. However, there are some disadvantages to take into account. In some cases, it is impossible to carry on the reaction in the presence of water as well as other impurities such as fatty acids. Some of these catalysts (solid resins) get deactivated with water; therefore, the raw material must be refined oil. In other situations, the catalyst could treat some amount of water and fatty acid, but the reaction time is so large that is not of industrial interest (Marchetti & Errazu, 2010 b).
Enzymes seem to be the best option, for being environmentally friendly. They are produced in the nature; they require not drastic conditions to work and it could treat some impurities in the raw material. It should be considered that reaction temperature could not be too high, otherwise the organisms will die. Some water is needed it to start the reaction, but too much water will deactivated the catalyst. This one will allow the transesterification as well as the esterification reaction to take place simultaneously. On the other side, the reaction time for both reactions could be considered as too long in comparison with other options and the price of this catalyst is extremely high, making it a very non competitive alternative (Antczak et al, 2009, Rodrigues et al., 2008, Dalla Rosa et al., 2008, Dizge et al., 2009). Because of this, new enzymes as well as new enzyme technologies are being developed in a daily basis aiming to reduce the price, improving the catalytic properties and find a way of reusing it over and over again so its price could be depreciated over time.
Nowadays, one of the fastest technologies available uses supercritical alcohols, either methanol or ethanol. In this case, the reaction temperature and reaction pressure provoke the alcohol to be in a supercritical state, and therefore, not catalyst is required. Thanks to this technology, a full conversion of non high quality oils could be reached in less than 5 minutes (Demirbaş, 2002, 2003, Saka & Kusdiana, 2001, Kusdiana & Saka, 2001, 2004, Hawash et al., 2009, Gui et al., 2008, Kasim et al. 2009). The absence of a catalyst allows the system to treat triglycerides, fatty acids, and water with no concerns. Even more, in order to reduce the amount of alcohol, some works have shown that is possible to reduce the alcohol molar ratio by increasing secondary supercritical fluids such as CO2, hexane, heptanes, propane or tetrahydrofuran, being those much cheaper (Sawangkeaw et al., 2007, Tan et al., 2010, Yin et al., 2008, Han et al., 2005). In some cases, it could be found that a catalyst could be introduced into the system (Demirbaş, 2007) making possible to achieved good final conversions without compromising the down streaming separation and purification. For this process, less equipment is required and the purity of the final biodiesel and glycerin are quite good. Nevertheless, there is a need of high temperature and pressure that implies a high operational cost and makes this technology less attractive than others. But, when considering the process with different approaches it will become more economically viable (van Kasteren & Nisworo, 2007, Deshpande et al., 2010, Lim et al., 2009)
The use of membrane reactors as well as monolithic catalysts, and monolithic reactors are among the new options that being considered. Each of them has major advantages and disadvantages over the conventional process. The monolithic reactors (Kolaczkowski et al., 2009, Dizge et al., 2009, Tonetto & Marchetti, 2010), produced from powder of a basic catalyst, have as major concern the leaching of the catalyst from the heterogeneous phase to the homogeneous phase. Under this circumstance, the activity o the catalyst is lost, and also there is a need of purification and separation of the products from the catalyst. However, if the leaching problem is solved, the reaction will be more environmentally friendly and the Biodiesel produced will be of better quality. Membrane reactors have been widely used for the water gas shift reaction with great results (Dubé et al. 2007, Baroutian et al., 2011, Zhu et al., 2010, Cheng et al., 2010, Cao et al., 2008). Dubé et al. (Dubé et al., 2007) used them and succeeded in producing a final product of high quality. The catalyst employed was a homogeneous basic one; so we should consider that the separation of alcohol and other compounds, from the main flow, could be quite complicated, and the general price for the membrane is sometimes too high.
In order to compare the variables previously described, we selected those that are considered to be the most relevant and presented them in Table 8, were we show them in relation to the different technologies.
Based on Table 8, we can say that in all the cases, except from the base technology will produce ester from the presence of fatty acid. However, not all of them have the same effect when water is in the system, as it is in the case of solid resin and enzyme, where water could have a negative effect. In the case of monolithic, the leaching is due to the contact with a liquid phase, that is not necessarily water, and therefore, the effects of water itself are yet unknown.
The reaction temperature is quite low for the base, acid and enzymatic process, but could be quite high for the other three options. This is one of the main reasons for the cost of the technology to be from affordable to expensive. In the case of enzymes, even though the reaction temperature is quite low, the cost of the catalyst makes the general investment significant, and in some cases, making the technology not viable.
The purification of ester, its quality, and the quality of the produced glycerin are related to the type of technology used, especially when the catalyst is in homogeneous phase. In the last case, the catalyst needs to be separated and neutralization, separation, and purification of the products are required. For all the heterogeneous as well as the non catalytic alternatives, the need of purification is simpler and the need of equipment is also lower. In the case of the monolithic reactor, the leaching problem could make this technology less
|Products from FFA||Soaps||Esters||Esters||Esters||Esters||Esters|
|Effect of Water*|
|Yield to ester||Normal||High||High||Normal||Good||Normal|
|Purification of glycerol||Difficult||Simple||Simple||Simple||Simple||Difficult|
|Reaction time+||1-2 h||8-70 h||4-10 min||6 h||variable||4-70 h|
|Amount of equipment||High||Low||Low||Low||Low||High|
suitable due to the possibility of separation and purification. So far this problem has been presented (Tonetto & Marchetti, 2010) but not much has been done in order to solve it; even though it is considered that this disadvantage might be easier to overcome.
In all the technologies studied, the yield for biodiesel is high, even thought in some cases this is much higher.
In this chapter it has been presented different types of process for biodiesel production, their advantages and disadvantages as regards the different operational variables, the different raw material qualities, and the different catalysts employed.
Due to these differences, it is not easy to select a process to use. Several operational conditions and many economic variables should be considered together with those presented in Table 9, before choosing the best alternative for each case.
About the type of vegetable oil and its quality, it is important to remember that in order not to compete with the vegetable oil for feeding purposes, the oil used is in all cases is inedible and/or waste oil. Due to the high amount of free fatty acid that might be present on the waste oil, some technologies are more suitable than suitable than others. That is the case of supercritical alcohols over conventional process. A combination of several options produces much more reliable and environmental friendly processes. However, in those cases, the need for a much more control over other influenciable variables is stronger. When using a vegetable oil, the availability of the oil and the proximity of the plantations is also a key factor and together with a clear local policy, such as tax reduction. This will help the biodiesel companies but at the same time, it will provoke an increase in the price of the oil directly related to the need of these raw materials.
The use of waste oils should be a must. To achieve this, several options could be used based on the key factors previously explained. The use of waste oils helps to consume pollutants, does not interfere in the Fuel vs. Food debate, and demands an environmentally friendly process.