Classification of Polymers
Classification of Polymers
Classification of Polymers
Subject: Chemistry
Paper code: CH101
Stream: B.Tech
Semester: 1st
Presented by
Dr. Rupa Bhattacharyya
M.Tech, PhD (Tech)
Assistant Professor
Department of Basic Science & Humanities
Narula Institute of Technology
Classification of Polymers
• Origin
• Chemical structure
• Polymeric structure
• Tacticity
• Molecular forces
• Thermal response
Natural polymers –
Nature made polymers
Eg. Natural rubber, cellulose,
starch, proteins, silk, etc.
Synthetic polymers –
Man made polymers
Eg. Polyethylene, polypropylene,
PVC, nylon, polyester, etc.
Homopolymers – A (monomer)
Polymers which are
made up of a single
kind of monomer -A-A-A-A-A-A-
Eg. PE, PP, PVC, ……
PS, etc.
Chemical
structure
Copolymers – A (monomer 1)
Polymers which are +
B (monomer 2)
made up of more than
one kind of monomer
Eg. Styrene-butadiene
rubber (SBR),
Acrylonitrile-butadiene A-A-B-A-B-A-A-B-….
rubber (NBR), etc.
Linear
Eg. HDPE
Polymeric
structure Branched
Eg. LDPE
Cross linked
Eg. Bakelite,
vulcanized
rubber
Isotactic
(-d-d-d-d- or –l-l-l-l-
configuration of the
chiral carbon
Tacticity Syndiotactic
-d-l-d-l-
configuration of
the chiral carbon
Atactic
random
configuration
Tacticity
Tacticity is the relative stereochemistry of adjacent chiral centers within a macromolecule. The practical
significance of tacticity rests on the effects on the physical properties of the polymer. A vinyl and related
polymer ( CH2 – CHR ) is characterized by an asymmetric carbon atom (marked with a little asterisk on it)
in each of the repeat units of its chain molecules and a type of stereochemical difference that may arise in
the segments of the chain is d –, l – isomerism. Tacticity has to do with which side of the chain the R
group is placed. Fischer projections can be used to show the three different types of tacticity.
• Isotactic:
When all of the R groups line up on the same side then the polymer is known as isotactic polymer.
Considering head to tail linkage of the repeat units, the stereo sequences may be all – d– or all – l –
sequences, identified in terms of tacticity or spatial disposition of the substituent group, R as isotactic ;
(like sequences) ( – d – d – d – d – ) Or – ( – l – l – l – l – )
• Syndiotactic
In this case the R groups alternate from side to side which is known as syndiotactic polymer. For alternate
appearance of d – and l – sequences, the relevant polymer is called syndiotactic. The syndiotactic
sequence or stereoisomer may be represented as (Alternate sequences; ( – d – l – d – l – d –)
• Atactic:
A third distinguishable long chain sequence called atactic sequence would be given by a random spatial
disposition of the substituent – R groups, also exemplified by a random mix of isotactic and syndiotactic
sequences, viz.
(Random sequence, ( – d – d – l – d – l – l –)
Elastomers
(weak intermolecular force)
Eg. Natural rubber, Buna S,
Buna N, CSP, etc.
Molecular Plastics
(moderate intermolecular
forces force)
Eg. PE, PP, PVC, nylon,
polyester, etc.
Fibres
(strong intermolecular force)
Eg. Nylon, polyester, acrylics,
etc.
Thermoplastics
(Polymers which remain soluble and
fusible on repeated cycles of heating and
cooling)
Eg. PE, PP, PVC, PS, Nylon, etc.
Thermal
response
Thermosets
(One time use)
Eg. Bakelite, polycarbonates, urea-
formaldehyde,melamine formaldehyde,
etc.