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2.5.1.2 Alkali Catalysis

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The use of bases in transesterification is probably the most common practice of conversion of compatible feedstock (low in FFA and moisture) into esters. The conversion involves formation of an alkoxide ion from the base and the alcohol, which then targets the triglyceride (for example), attacking the carbonyl carbon, and forming a tetrahedral shaped intermediate. These compounds then undergo reaction with an alcohol molecule, undergoing a structural rearrangement during the process to give off an ester molecule and leading to the formation of a diglyceride [2]. This process will now repeat itself twice to finally yield glycerol as a by‐product along with 2 mol of alkyl ester [28], as shown in Figure 2.1. The process cannot tolerate even traces of FFA and moisture except for KOH, which is why it is favored over other bases. The process can also include homogeneous and heterogeneous catalysts, with doped basic groups being more stable compared to acidic groups [1, 6]. Many edible and nonedible oils (including waste oils) have been converted into biodiesel through this process; a select few of which are summarily presented in Table 2.2.

Table 2.2 Traditional catalyzed conversions using acids, bases, enzymes, or other catalysts.

Source: Modified from Ref. [2].

Feedstock Catalyst used Reaction conditions Yield/conversion (%) References
Reaction temperature (°C) Reaction time (h) Catalyst concentration (% w/w) Alcohol:oil (ratio or wt%) Agitation speed (rpm)
Acid‐catalyzed conversion
Castor oil H2SO4 50 1 1 20 : 1 700 90.83 [4]
Waste cooking oil H2SO4 60 3 5 12 : 1 800 95.376 [3]
Mahua oil Sulfonated Delonix regia char 50 1 4 6 : 1 1000 97.04 [5]
Castor oil Sulfonated MFL char 60 1.5 7 70 950 92 [16]
Base‐catalyzed conversion
Waste cooking oil KOH 50 1.67 0.75 9 : 1 90 [20]
Waste cooking oil CaO 75 1 5 9.8 : 1 450 96.6 [21]
Waste cooking oil CaO 65 3 7.5 15 : 1 1200 90 [22]
Waste cooking oil Calcined egg shells 65 5.5 3.5 22.5 : 1 600 91 [23]
Enzyme‐catalyzed conversion
Waste cooking oil Lipase 50 10 6 20 94 [24]
Jatropha oil Lipase 40 8 0.5 4 : 1 71 [25]
Other novel catalysts for conversion
Waste cooking oil Fe(II)‐doped anthill 60 1.5 1.2 6 : 1 99.73 [15]
Rubber seed oil Fe(II)‐doped Delonix regia char 40 15 5 3 : 1 500 96.31 [26]
Two‐step catalyzed conversion
Waste cooking oil H2SO4 65 3 1 3 : 7 400 21.5 [27]
NaOH 50 3 1 3 : 7 400 90.6
Karanja oil Sulfonated Delonix regia char 50 0.75 3 12 : 1 900 99.86 [6]
KOH‐doped Delonix regia char 60 1.5 4 6 : 1 700 99.39
Biodiesel Production

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