Project Class 12 On Polymers
Project Class 12 On Polymers
Secondary
Education
Chemistry project
polymers
Classification of
polymers
Structural polymers
• 1. Linear polymers on Structure These polymers
consist of long and straight chains. The examples of
Polymers are high density polythene, polyvinyl chloride,
etc.
Addition polymers
• Addition polymers are formed from repeated units of
monomer units possessing double and triple bonds.
• Polymers formed by addition of two different
polymers are called co-polymers
Condensation polymers
• The condensation polymers are formed by repeated
condensation reaction between two different bi-
functional or tri-functional monomeric units. In these
polymerisation reactions, the elimination of small
molecules such as water, alcohol, hydrogen chloride,
etc. take place. • The examples are terylene (dacron),
nylon 6, 6, nylon 6, etc. For example, nylon 6, 6 is
formed by the condensation of hexamethylene diamine
with adipic acid.
Classification of polymers based
on molecular forces
elastomers
Fibers
• Fibres are the thread forming solids which possess
high tensile strength and high modulus. These
characteristics can be attributed to the strong
intermolecular forces like hydrogen bonding.
• These strong forces also lead to close packing of
chains and thus impart crystalline nature. The examples
are polyamides (nylon 6, 6), polyesters (terylene), etc.
Thermoplastic polymers
• These are the linear or slightly branched long chain
molecules capable of repeatedly softening on heating
and hardening on cooling. These polymers possess
intermolecular forces of attraction intermediate
between elastomers and fibres. Some common
thermoplastics are polythene, polystyrene, polyvinyls,
etc
Thermosetting polymers
• These polymers are cross linked or heavily branched
molecules, which on heating undergo extensive cross
linking in moulds and again become infusible. These
cannot be reused. Some common examples are
bakelite, urea-formaldelyde resins, etc.
copolymerisation
• Copolymerisation is a polymerisation reaction in
which a mixture of more than one monomeric species
is allowed to polymerise and form a copolymer. The
copolymer can be made not only by chain growth
polymerisation but by step growth polymerisation also.
It contains multiple units of each monomer used in the
same polymeric chain. For example, a mixture of 1, 3 –
butadiene and styrene can form a copolymer.
RUBBER
1. Natural rubber
• Rubber is a natural polymer and possesses elastic
properties. It is also termed as elastomer and has a
variety of uses. It is manufactured from rubber latex
which is a colloidal dispersion of rubber in water. •
Natural rubber may be considered as a linear polymer
of isoprene (2-methyl-1, 3- butadiene) and is also
called as cis – 1, 4 – polyisoprene.
• Vulcanisation of rubber:
Natural rubber becomes soft at high temperature
(>335 K) and brittle at low temperatures (On
vulcanisation, sulphur forms cross links at the reactive
sites of double bonds and thus the rubber gets
stiffened. The probable structures of vulcanised rubber
molecules are depicted below:
Preparation of synthetic
rubbers
• 1. Neoprene
Neoprene or polychloroprene is formed by the free
radical polymerisation of chloroprene.
2. Buna – N
Buna –N is obtained by the copolymerisation of 1, 3 –
butadiene and acrylonitrile in the presence of a
peroxide catalyst.
Biodegradable polymers
Classification based on
growth polymers
• There are two broad types of polymerisation
reactions, i.e., the addition or chain growth
polymerisation and condensation or step growth
polymerisation.
Addition Polymerisation or Chain Growth
Polymerisation
• In this type of polymerisation, the molecules of the
same monomer or diferent monomers add together on
a large scale to form a polymer. The monomers used
are unsaturated compounds, e.g., alkenes, alkadienes
and their derivatives. This mode of polymerisation
leading to an increase in chain length or chain growth
can take place through the formation of either free
radicals or ionic species. However, the free radical
governed addition or chain growth polymerisation is
the most common mode.
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