BIO FUEL

6H2O + 6CO2 => C6H12O6 + 6O2
Palm oil is used to produce biofuel. .
A process known as transesterification is commonly used to produce
biodiesel. Chemically, transesterification is the process of exchanging
the alkyl group of an ester with another alkyl group, from a different
alcohol. Vegetable oil contains fatty acids bonded to glycerol to form
triglycerides. In the case of biodiesel, a vegetable oil ester is
combined with a simple alcohol, methanol, and a catalyst, resulting in
the breakup of the triglyceride ester to form glycerol and three methyl
esters (biodiesel) A typical molecule of biodiesel looks like the
structure below. Mostly it is a
long chain of carbon atoms, with hydrogen atoms attached, and at one
end is what wecall an ester functional group .

If soap gets made, then later it
complicates the steps after the transesterication reaction that are
needed to separate the biodiesel from leftover methanol, the NaOH or KOH
catalyst, and the glycerol byproduct.Diesel engines can burn biodiesel
fuel with no modifications (except for replacing some rubber tubing that
may soften with biodiesel). This is possible because biodiesel is chemically very similar to regular diesel, shown below. Notice
that regular diesel also has the long chain of carbon and hydrogen
atoms, but doesn’t have the ester group.Actually, the first diesel
engines didn’t run on “diesel” fuel, but on vegetable oil, a sample
molecule of which is shown below. Notice
that it also has the long rows of carbon and hydrogen atoms, but is
about three times larger than normal diesel molecules. It
also has ester functional groups , like biodiesel.That larger size of
vegetable oil means that in cold weather it gels, making it hard to use
in an engine. Converting it
into biodiesel makes it a smaller molecule, closer to the size of
regular diesel, so that it has to get colder than vegetable oil before
it starts to gel.
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