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Revision: Std XII >> Introduction to Polymer Chemistry MAH-MHT CET (PCM/PCB) Introduction to Polymer Chemistry

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Definitions [9]

Answer the following in one sentence.

Define the term: Monomer

Small molecules that are interlinked together to form polymers are called as monomers.

Define thermosetting polymers with two examples of them.

Thermosetting polymers are cross-linked or heavily branched polymers which get hardened during the molding process. These plastics cannot be softened again on heating. Examples of thermosetting plastics include bakelite, urea-formaldehyde resins.

Define fibres.

Polymeric solids which form threads are called fibres.

Define elastomer.

Polymers having the property of elasticity in which a substance gets stretched by external force and restores its original shape on the release of that force are called elastomers.

Answer the following in one sentence.

Define the term: Synthetic fibres

The man-made fibres prepared by polymerization of one monomer or copolymerization of two or more monomers are called synthetic fibres.

Define Polymer.

A polymer is a large molecule of very high molecular mass formed by the repeated combination of a very large number of one or more types of small molecules called monomers.

Answer the following in one sentence.

Define the term: Vulcanization

The process by which a network of cross-links is introduced into an elastomer is called vulcanization.

Define rubber.

Polymers which are elastic in nature are called rubber.

Definition: Vulcanisation

The process by which a network of cross links is introduced into an elastomers is called vulcanisation.

Key Points

Key Points: Polymer Chemistry
  • Polymers are very large molecules formed by joining many small molecules, having a high molecular mass.
  • The small repeating units that make up polymers are called monomers.
  • Monomers are linked together by covalent bonds to form long chains.
  • The process of joining monomers to form a polymer is called polymerisation.
Key Points: Classification of Polymers> Based on Source or Origin
  • Polymers are classified based on their source or origin into three types: natural, semi-synthetic, and synthetic polymers.
  • Natural polymers are obtained from plants and animals, such as cellulose, starch, proteins, cotton, and silk.
  • Semi-synthetic polymers are chemically modified forms of natural polymers, e.g., cellulose acetate and cellulose nitrate (rayon).
  • Synthetic polymers are man-made and prepared in laboratories by polymerisation, such as nylon, polythene, Teflon, and Bakelite.
  • Synthetic polymers are further used to make fibres, rubbers, and plastics, which have wide industrial applications.
Key Points: Classification of Polymers> Based on Structure
  • Polymers can be classified based on structure into linear, branched, and cross-linked (network) polymers.
  • Linear polymers have long, straight chains of monomers joined in a line; e.g., HDPE, PVC, polystyrene.
  • Branched polymers have a main chain with side branches of different lengths; e.g., LDPE, polypropylene.
  • Cross-linked (network) polymers have chains connected by strong covalent bonds, forming a 3D network structure.
  • Cross-linked polymers are hard and rigid due to strong bonding; common examples include Bakelite and melamine.
Key Points: Classification of Polymers> Based on Mode of Polymerisation
  • Polymers are classified based on the mode of polymerisation into addition (chain growth), condensation (step growth), and ring-opening polymerisation.
  • Addition polymerisation involves repeated addition of monomers (with double/triple bonds) without loss of small molecules; e.g., Teflon, PAN.
  • Condensation polymerisation occurs between bi-functional or polyfunctional monomers with elimination of small molecules like water or alcohol; e.g., Nylon, Terylene.
  • Ring-opening polymerisation involves polymerisation of cyclic monomers to form long chains, usually without elimination of small molecules; e.g., caprolactam.
Key Points: Classification of Polymers> Based on Intermolecular Forces
  • Polymers can be classified based on intermolecular forces into elastomers, fibres, thermoplastics, and thermosetting polymers.
  • Elastomers have the weakest intermolecular forces, making them flexible and elastic; e.g., natural rubber, Buna-S.
  • Fibres have strong intermolecular forces (like hydrogen bonding), giving them high tensile strength; e.g., Nylon-6, Terylene, PAN.
  • Thermoplastics have weak van der Waals forces, so they can be softened and reshaped on heating; e.g., polythene, polystyrene.
  • Thermosetting polymers have strong cross-linked structures, making them hard and rigid; e.g., Bakelite, melamine.
    Strength order: Elastomers < Thermoplastics < Fibres < Thermosetting polymers.
Key Points: Classification of Polymers> Based On Type of Different Monomers
  • Polymers can be classified based on the type of monomers into homopolymers and copolymers (heteropolymers).
  • Homopolymers are formed from only one type of monomer repeated many times; e.g., polythene, Nylon-6, PAN.
  • Copolymers (heteropolymers) are formed from two or more different types of monomers.
  • Copolymers show combined properties of different monomers; e.g., Buna-S (from butadiene and styrene), Buna-N.
Key Points: Classification of Polymers> Based on Biodegradability

Polymers are classified as biodegradable or non-biodegradable based on their biodegradability.

1. Biodegradable Polymers

  • Meaning: Polymers that decompose by microorganisms or enzymes.
  • Nature: Environment-friendly, as they break down naturally.
  • Examples: PHBV, Nylon-2–Nylon-6.
  • Special point: PHBV is a copolymer used in packaging, medical devices, and drug delivery.
  • Use: Helps reduce environmental pollution.

2. Non-Biodegradable Polymers

  • Meaning: Polymers that do not decompose by microorganisms.
  • Nature: Persist in the environment for a long time.
  • Examples: Polythene (LDPE, HDPE), Teflon, Nylon-6,6, PAN.
  • Use: Widely used in plastics, fibres, containers, insulation, etc.
  • Disadvantage: Causes environmental pollution due to slow decomposition.
Key Points: Some Important Polymers
Polymer Monomer(s) Uses
Natural Rubber (Polyisoprene) Isoprene (2-methyl-1,3-butadiene) Exhibits elastic property
Neoprene Chloroprene (2-chloro-1,3-butadiene) Conveyer belts
Buna-S 1,3-Butadiene + Styrene Bubblegums, tyres
Buna-N 1,3-Butadiene + Acrylonitrile Rubber belts, shoe soles, O-rings, gaskets
Polypropene Propene Ropes, toys, pipes, fibres
Polystyrene Styrene Insulator, wrapping material, toys, radio & TV cabinets
PVC Vinyl chloride Rain coats, handbags, vinyl flooring, water pipes
Glyptal Ethylene glycol + Phthalic acid Paints and lacquers
Bakelite Phenol + Formaldehyde Combs, phonograph records, electrical switches, wooden planks
Nylon 6,6 Adipic acid + Hexamethylenediamine Fabrics, ropes, tyre cords
Nylon 6 ε-Caprolactam Fabrics, ropes
Terylene / Dacron Ethylene glycol + Terephthalic acid Fibres, safety belts, tents
Melamine-formaldehyde Melamine + Formaldehyde Unbreakable crockery
Urea-formaldehyde resin Urea + Formaldehyde Unbreakable cups, laminated sheets
Key Points: Commercially Important Polymers
Polymer Monomer(s) Uses
Perspex / Acrylic glass Methyl methacrylate Lenses, paint, LCD screen, shatter-resistant glass
Buna-N Butadiene + Acrylonitrile Adhesives, rubber belts, shoe soles, O-rings, gaskets
PVC Vinyl chloride Water pipes, rain coats, and flooring
Polyacrylamide Acrylamide Electrophoresis gel
Urea-formaldehyde resin Urea + Formaldehyde Unbreakable dinnerware, decorative laminates
Glyptal Ethylene glycol + Phthalic acid Paints and lacquers
Polycarbonate Bisphenol + Phosgene Electrical & telecom hardware, food-grade plastic containers
Thermocol (Polystyrene) Styrene Non-biodegradable; styrene leaches on heating — banned
Teflon Tetrafluoroethylene Non-stick cookware, chemical resistance
Polyacrylonitrile (PAN) Acrylonitrile Wool substitute, textiles
Melamine-formaldehyde Melamine + Formaldehyde Unbreakable crockery
Bakelite Phenol + Formaldehyde Combs, electrical switches, wooden planks, lacquers
Key Points: Vulcanisation of Rubber
  • Vulcanisation of rubber is the process of introducing cross-links between polymer chains in an elastomer.
  • It is done by heating natural rubber with sulphur and additives at a temperature of 373 K to 415 K.
  • Sulphur forms cross-links at the double bonds of polyisoprene chains.
  • Vulcanisation makes rubber stronger, less sticky, and more resistant to swelling by organic liquids.
  • It also improves the elasticity and durability of rubber for practical use.
Key Points: Molecular Mass and Degree of Polymerization of Polymers
  • Molecular mass of a polymer is the average molecular mass of all its polymer chains.
  • Molecular mass depends on the degree of polymerisation (DP).
  • Degree of polymerisation (DP) is the number of repeating monomer units in a polymer chain.
  • Higher DP means higher molecular mass and generally stronger polymer properties.
  • Polymers with hydrogen bonding require lower DP to achieve stability compared to those with weak intermolecular forces.
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