Читать книгу Encyclopedia of Renewable Energy - James Speight G., James G. Speight - Страница 161

Transesterification reactions can be catalyzed by alkalis or enzymes. The catalytic transesterification of vegetable oils with methanol is an important industrial method used in biodiesel synthesis. Also known as methanolysis, this reaction is well established using acids or alkalis, such as sulfuric acid or sodium hydroxide as catalysts. However, these catalytic systems are less active or completely inactive for long chain alcohols. Usually, industries use sodium or potassium hydroxide or sodium or potassium methoxide as catalyst since they are relatively cheap and quite active for this reaction. Enzyme-catalyzed procedures, using lipase as catalyst, do not produce side reactions, but the lipases are expensive for industrial-scale production and a three-step process was required to achieve a 95% conversion. The acid-catalyzed process (Table B-7) is useful when a high amount of free acids is present in the vegetable oil, but the reaction time is on the order of 48 to 96 hours, even at the boiling point of the alcohol, and a high molar ratio of alcohol was needed (20:1 wt/wt to the oil).

Table B-7 Schematic of the catalytic transesterification process for biodiesel production.

Feedstock	Reactor	Products
Vegetable oil	Catalyst	Biodiesel
Methanol*		Glycerol
*Ethanol may also be used.

The transesterification process is catalyzed by alkaline metal alkoxides, and hydroxides, as well as sodium or potassium carbonates. Alkali-catalyzed transesterification with short-chain alcohols, for example, generates high yields of methyl esters in short reaction times. The alkaline catalysts show high performance for obtaining vegetable oils with high quality, but a question often arises; that is, the oils contain significant amounts of free fatty acids which cannot be converted into biodiesels but to a lot of soap. These free fatty acids react with the alkaline catalyst to produce soaps that inhibit the separation of the biodiesel, glycerin, and wash water. Triglycerides are readily transesterified in a batch operation in the presence of alkaline catalyst at atmospheric pressure and at a temperature of approximately 60 to 70°C (140 to 160°F) with an excess of methanol. It often takes at least several hours to ensure the alkali (NaOH or KOH) catalytic transesterification reaction is complete. Moreover, removal of these catalysts is technically difficult and brings extra cost to the final product. Nevertheless, these methods are a good alternative since they can give the same high conversions of vegetable oils just by increasing the catalyst concentration to 1 or 2 mol%. Alkaline metal alkoxides (as CH₃ONa for the methanolysis) are the most active catalysts since they give high yields (> 98%) in short reaction times (30 min) even if they are applied at low molar concentrations (0.5 mol%).

The transesterification process is catalyzed by sulfuric, hydrochloric, and organic sulfonic acids. In general, acid-catalyzed reactions are performed at high alcohol-to-oil molar ratios, low-to-moderate temperatures and pressures, and high acid catalyst concentrations. These catalysts give high yields in alkyl esters, but these reactions are slow, requiring typically temperature above 100°C (212°F) and more than 3 h to complete the conversion. Studies of the acid-catalyzed system have been limited in number. Despite the relatively slow reaction rate, the acid-catalyzed process offers benefits with respect to its independence from free fatty acid content and the consequent absence of a pretreatment step. These advantages favor the use of the acid-catalyzed process when using waste cooking oil as the raw material.

Enzyme-catalyzed reactions (such as lipase-catalyzed reactions) have advantages over traditional chemical-catalyzed reactions: the generation of no by-products, easy product recovery, mild reaction conditions, and catalyst recycling. Also, enzymatic reactions are insensitive to free fatty acids and water content in waste cooking oil. As for the enzyme-catalyzed system, it requires a much longer reaction time than the other two systems. The enzyme reactions are highly specific and chemically clean. Because the alcohol can be inhibitory to the enzyme, a typical strategy is to feed the alcohol into the reactor in three steps of 1:1 mole ratio each. The reactions are slow, with a three-step sequence requiring from 4 to 40 hours, or more. The reaction conditions are modest, from 35 to 45°C (95 to 113°F). The main problem of the enzyme-catalyzed process is the high cost of the lipases used as catalyst.

Synthesis of biodiesel using enzymes such as Candida antarctica, Candida rugasa, Pseudomonas cepacia, immobilized lipase (Lipozyme RMIM), Pseudomonas sp., and Rhizomucor miehei is well reported in the literature. In the previously mentioned work (Shah and Gupta, 2007), the best yield 98% (w/w) was obtained by using Pseudomonas cepacia lipase immobilized on celite at 50°C in the presence of 4–5% (w/w) water in 8 hours.