Petrochemicals and Polymers
Petrochemicals and Polymers
Petrochemicals and Polymers
Petroleum itself as a mixture isn't very useful but each component part of the mixture,
called a fraction, is useful and each fraction has different applications
The fractions in petroleum are separated from each other in a process
called fractional distillation
The molecules in each fraction have similar properties and boiling points, which depend
on the number of carbon atoms in the chain
The boiling point and viscosity of each fraction increases as the carbon chain gets
longer
Diagram showing the process of fractional distillation to separate crude oil in a fractionating
column
Explanation
Viscosity: This refers to the ease of flow of a liquid. High viscosity liquids are thick and
flow less easily. If the number of carbon atoms increases, the attraction between the
hydrocarbon molecules also increases which results in the liquid becoming more viscous
with the increasing length of the hydrocarbon chain. The liquid flows less easily with
increasing molecular mass
Colour: As carbon chain length increases the colour of the liquid gets darker as it gets
thicker and more viscous
Melting point/boiling point: As the molecules get larger, the intermolecular attraction
becomes greater. So more heat is needed to separate the molecules. With increasing
molecular size there is an increase in boiling point
Volatility: Volatility refers to the tendency of a substance to vaporise. With increasing
molecular size hydrocarbon liquids become less volatile. This is because the attraction
between the molecules increases with increasing molecular size
Carbohydrates, proteins and silk are examples of natural polymers while nylon and terylene are
synthetic (man-made) polymers. There are two reactions to form polymers and those are:
1. Addition polymerization
2. Condensation polymerization
For example, the addition polymerization of ethene to form poly(ethene) is shown below.
As you can see in the image, the carbon-carbon double covalent bonds of ethene break (due to
high temperature and pressure). The n indicates multiple monomers. When these monomers
break, they combine to form poly(ethene).
Addition polymerization (as discussed above) is very important because poly(ethene) is used to
make various toys, plastic bags and various other instruments due to its properties.
Nylon and terylene are made due to condensation polymerization. Organic chemistry requires
you to learn how monomers react to form nylon and terylene.
It is to note that there is an amide linkage in the condensation polymerization to form nylon
(because of the presence of diamine) while there is an ester linkage in the condensation
polymerization to form terylene
Now, I will show you the condensation polymerization to form nylon. Therefore, you can
consult the structure below for your guidance (note that the repeating amide links can be seen
in nylon).
You should remember that nylon and proteins have the same amide linkage even though nylon
is a synthetic polymer while proteins are natural polymers.
Similarly, terylene (a synthetic polymer) and fats (a natural polymer) have the same ester
linkage which is visible in their structural formula.