The
mechanism that I'll be presenting here it's a simple process that
anyone can do it by themselves. It is called transesterification and is
summed up as the reaction of an oil with an alcohol to form esters and
glycerol.
Transesterification reaction (Fangrui et al, 1999) |
First
we will analyse the right side of the chemical equation. Among the
alcohols that can be used in the transesterification process are
methanol, ethanol, propanol, butanol and amyl alcohol. Methanol and
ethanol are used most frequently, especially methanol because of its
low-cost and its physical and chemical advantages. We will use methanol
in our process. This chemical is toxic so take the necessary protections
when handling it. Regarding the oil we can use a diversity of wide
commercial oils.
In the next part of this article we will discuss the production itself.
As we saw here it is pretty simple to make biodiesel at home regarding
the products that you need to this process.
To
industry is more interesting to use already used oils, for example food
oils. In this case we would be recycling a very prejudicial compound to
the environment when it is thrown to the hydric resources. In our case
we will use commercial available soya oil.
Now,
in the left side of the equation we have two important compounds,
esters, that are our biodiesel and glycerol, an important compound
largely used in the industry. So we conclude that we have to separate
efficiently the two compounds. We will use a basic step of gravitational
settling to separate this two products.
The
last chemical compound used in this reaction is the catalyst. A
catalyst is usually used to improve the reaction rate and yield. Because
the reaction is reversible, excess alcohol is used to shift the
equilibrium to the products side.We will use NaOH as a catalyst in this
reaction. The benefits of using a catalyst are enormous but we encounter
a problem that is the water formation. This formation of water can lead
to a process called saponification where the esters are attacked by -OH
ions in the presence of water. This reaction is undesirable to our
process and must be avoided.
Saponification reaction |
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