Polymers
“Copolymerisation has been used by nature in polypeptides which may contain as many as 20 different amino acids. Chemists are still far behind”.
Do you think that daily life would have been easier and colourful without the discovery and varied applications of polymers? The use of polymers in the manufacture of plastic buckets, cups and saucers, children’s toys, packaging bags, synthetic clothing materials, automobile tyres, gears and seals, electrical insulating materials and machine parts has completely revolutionised the daily life as well as the industrial scenario. Indeed, the polymers are the backbone of four major industries viz. plastics, elastomers, fibres and paints and varnishes. The word ‘polymer’ is coined from two Greek words: poly means many and mer means unit or part. The term polymer is defined as very large molecules having high molecular mass (103-107u). These are also referred to as macromolecules, which are formed by joining of repeating structural units on a large scale. The repeating structural units are derived from some simple and reactive molecules known as monomers and are linked to each other by covalent bonds. This process of formation of polymers from respective monomers is called polymerisation. The transformation of ethene to polythene and interaction of hexamethylene diamine and adipic acid leading to the formation of Nylon 6, 6 are examples of two different types of polymerisation reactions.
15.1 Classification of Polymers
There are several ways of classification of polymers based on some special considerations. The following are some of the common classifications of polymers:
15.1.1 Classification Based on Source
Under this type of classification, there are three sub categories.
1. Natural polymers
These polymers are found in plants and animals. Examples are proteins, cellulose, starch, resins and rubber.
2. Semi-synthetic polymers
Cellulose derivatives as cellulose acetate (rayon) and cellulose nitrate, etc. are the usual examples of this sub category.
3. Synthetic polymers
A variety of synthetic polymers as plastic (polythene), synthetic fibres (nylon 6,6) and synthetic rubbers (Buna – S) are examples of man-made polymers extensively used in daily life as well as in industry.
There are three different types based on the structure of the polymers.
1. Natural polymers
These polymers are found in plants and animals. Examples are proteins, cellulose, starch, resins and rubber.
2. Semi-synthetic polymers
Cellulose derivatives as cellulose acetate (rayon) and cellulose nitrate, etc. are the usual examples of this sub category.
3. Synthetic polymers
A variety of synthetic polymers as plastic (polythene), synthetic fibres (nylon 6,6) and synthetic rubbers (Buna – S) are examples of man-made polymers extensively used in daily life as well as in industry.
There are three different types based on the structure of the polymers.
15.1.2 Classification Based
1. Linear polymers on Structure
These polymers consist of long and straight chains. The examples of Polymers are high density polythene, polyvinyl chloride, etc. These are represented as:
These polymers consist of long and straight chains. The examples of Polymers are high density polythene, polyvinyl chloride, etc. These are represented as:
2. Branched chain polymers
These polymers contain linear chains having some branches, e.g., low density polythene. These are depicted as follows:
These polymers contain linear chains having some branches, e.g., low density polythene. These are depicted as follows:
3. Cross linked or Network polymers
These are usually formed from bi-functional and tri-functional monomers and contain strong covalent bonds between various linear polymer chains, e.g. bakelite, melamine, etc. These polymers are depicted as follows:
These are usually formed from bi-functional and tri-functional monomers and contain strong covalent bonds between various linear polymer chains, e.g. bakelite, melamine, etc. These polymers are depicted as follows:
15.1.3 Classification Based on Mode of Polymerisation
Polymers can also be classified on the basis of mode of polymerisation into two sub groups.
1. Addition polymers
The addition polymers are formed by the repeated addition of monomer molecules possessing double or triple bonds, e.g., the formation of polythene from ethene and polypropene from propene. However, the addition polymers formed by the polymerisation of a single monomeric species are known as homopolymers, e.g.,
polythene.
The addition polymers are formed by the repeated addition of monomer molecules possessing double or triple bonds, e.g., the formation of polythene from ethene and polypropene from propene. However, the addition polymers formed by the polymerisation of a single monomeric species are known as homopolymers, e.g.,
polythene.
The polymers made by addition polymerisation from two different monomers are termed as copolymers, e.g., Buna-S, Buna-N, etc.
2. 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.
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.
Example 15.1
Solution
It is a homopolymer and the monomer from which it is obtained is styrene C6H5CH = CH2.
Solution
It is a homopolymer and the monomer from which it is obtained is styrene C6H5CH = CH2.
15.1.4 Classification Based on Molecular Forces
A large number of polymer applications in different fields depend on their unique mechanical properties like tensile strength, elasticity, toughness, etc. These mechanical properties are governed by intermolecular forces, e.g., van der Waals forces and hydrogen bonds, present in the polymer. These forces also bind the polymer chains. Under this category, the polymers are classified into the following four sub groups on the basis of magnitude of intermolecular forces present in them.
1. Elastomers
These are rubber – like solids with elastic properties. In these elastomeric polymers, the polymer chains are held together by the weakest intermolecular forces. These weak binding forces permit the polymer to be stretched. A few ‘crosslinks’ are introduced in between the chains, which help the polymer to retract to its original position after the force is released as in vulcanised rubber. The examples are buna-S, buna-N, neoprene, etc.
These are rubber – like solids with elastic properties. In these elastomeric polymers, the polymer chains are held together by the weakest intermolecular forces. These weak binding forces permit the polymer to be stretched. A few ‘crosslinks’ are introduced in between the chains, which help the polymer to retract to its original position after the force is released as in vulcanised rubber. The examples are buna-S, buna-N, neoprene, etc.
2. Fibres
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.
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.
3. 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.
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.
4 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.
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.
15.1.5 Classification Based on Growth Polymerisation
The addition and condensation polymers are nowadays also referred as chain growth polymers and step growth polymers depending on the type of polymerisation mechanism they undergo during their formation.
Intext Question
15.1 What are polymers ?
15.2 How are polymers classified on the basis of structure?
15.1 What are polymers ?
15.2 How are polymers classified on the basis of structure?
15.2 Types of Polymerization Reactions
There are two broad types of polymerisation reactions, i.e., the addition or chain growth polymerisation and condensation or step growth polymerisation.
15.2.1 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.
1. Free radical mechanism
A variety of alkenes or dienes and their derivatives are polymerised in the presence of a free radical generating initiator (catalyst) like benzoyl peroxide, acetyl peroxide, tert-butyl peroxide, etc. For example, the polymerisation of ethene to polythene consists of heating or exposing to light a mixture of ethene with a small amount of benzoyl peroxide initiator. The process starts with the addition of phenyl free radical formed by the peroxide to the ethene double bond thus generating a new and larger free radical. This step is called chain initiating step. As this radical reacts with another molecule of ethene, another bigger sized radical is formed. The repetition of this sequence with new and bigger radicals carries the reaction forward and the step is termed as chain propagating step. Ultimately, at some stage the product radical thus formed reacts with another radical to form the polymerised product. This step is called the chain terminating step. The sequence of steps may be depicted as follows:
Chain initiation steps
A variety of alkenes or dienes and their derivatives are polymerised in the presence of a free radical generating initiator (catalyst) like benzoyl peroxide, acetyl peroxide, tert-butyl peroxide, etc. For example, the polymerisation of ethene to polythene consists of heating or exposing to light a mixture of ethene with a small amount of benzoyl peroxide initiator. The process starts with the addition of phenyl free radical formed by the peroxide to the ethene double bond thus generating a new and larger free radical. This step is called chain initiating step. As this radical reacts with another molecule of ethene, another bigger sized radical is formed. The repetition of this sequence with new and bigger radicals carries the reaction forward and the step is termed as chain propagating step. Ultimately, at some stage the product radical thus formed reacts with another radical to form the polymerised product. This step is called the chain terminating step. The sequence of steps may be depicted as follows:
Chain initiation steps
Chain terminating step
For termination of the long chain, these free radicals can combine in different ways to form polythene. One mode of termination of chain is shown as under:
For termination of the long chain, these free radicals can combine in different ways to form polythene. One mode of termination of chain is shown as under:
2 Preparation of some important addition polymers
(a) Polythene
There are two types of polythene as given below:
(i) Low density polythene: It is obtained by the polymerisation of ethene under high pressure of 1000 to 2000 atmospheres at a temperature of 350 K to 570 K in the presence of traces of dioxygen or a peroxide initiator (catalyst). The low density polythene (LDP) obtained through the free radical addition and H-atom abstraction has highly branched structure. Low density polythene is chemically inert and tough but flexible and a poor conductor of electricity. Hence, it is used in the insulation of electricity carrying wires and manufacture of squeeze bottles, toys and flexible pipes.
(a) Polythene
There are two types of polythene as given below:
(i) Low density polythene: It is obtained by the polymerisation of ethene under high pressure of 1000 to 2000 atmospheres at a temperature of 350 K to 570 K in the presence of traces of dioxygen or a peroxide initiator (catalyst). The low density polythene (LDP) obtained through the free radical addition and H-atom abstraction has highly branched structure. Low density polythene is chemically inert and tough but flexible and a poor conductor of electricity. Hence, it is used in the insulation of electricity carrying wires and manufacture of squeeze bottles, toys and flexible pipes.
(ii) High density polythene: It is formed when addition polymerisation of ethene takes place in a hydrocarbon solvent in the presence of a catalyst such as triethylaluminium and titanium tetrachloride (Ziegler-Natta catalyst) at a temperature of 333 K to 343 K and under a pressure of 6-7 atmospheres. High density polythene (HDP) thus produced, consists of linear molecules and has a high density due to close packing. It is also chemically inert and more tougher and harder. It is used for manufacturing buckets, dustbins, bottles, pipes, etc.
(b) Polytetrafluoroethene (Teflon)
Teflon is manufactured by heating tetrafluoroethene with a free radical or persulphate catalyst at high pressures. It is chemically inert and resistant to attack by corrosive reagents. It is used in making oil seals and gaskets and also used for non – stick surface coated utensils.
Teflon is manufactured by heating tetrafluoroethene with a free radical or persulphate catalyst at high pressures. It is chemically inert and resistant to attack by corrosive reagents. It is used in making oil seals and gaskets and also used for non – stick surface coated utensils.
(c) Polyacrylonitrile
The addition polymerisation of acrylonitrile in presence of a peroxide catalyst leads to the formation of polyacrylonitrile. Polyacrylonitrile is used as a substitute for wool in making commercial fibres as orlon or acrilan.
The addition polymerisation of acrylonitrile in presence of a peroxide catalyst leads to the formation of polyacrylonitrile. Polyacrylonitrile is used as a substitute for wool in making commercial fibres as orlon or acrilan.
15.2.2 Condensation Polymerisation or Step Growth polymerisation
This type of polymerisation generally involves a repetitive condensation reaction between two bi-functional monomers. These polycondensation reactions may result in the loss of some simple molecules as water, alcohol, etc., and lead to the formation of high molecular mass condensation polymers.
In these reactions, the product of each step is again a bi-functional species and the sequence of condensation goes on. Since, each step produces a distinct functionalised species and is independent of each other, this process is also called as step growth polymerisation.
The formation of terylene or dacron by the interaction of ethylene glycol and terephthalic acid is an example of this type of polymerisation.
In these reactions, the product of each step is again a bi-functional species and the sequence of condensation goes on. Since, each step produces a distinct functionalised species and is independent of each other, this process is also called as step growth polymerisation.
The formation of terylene or dacron by the interaction of ethylene glycol and terephthalic acid is an example of this type of polymerisation.
Some important condensation polymerisation reactions characterised by their linking units are described below:
1. Polyamides
These polymers possessing amide linkages are important examples of synthetic fibres and are termed as nylons. The general method of preparation consists of the condensation polymerisation of diamines with dicarboxylic acids and also of amino acids and their lactams.
1. Polyamides
These polymers possessing amide linkages are important examples of synthetic fibres and are termed as nylons. The general method of preparation consists of the condensation polymerisation of diamines with dicarboxylic acids and also of amino acids and their lactams.
Preparation of nylons
(i) Nylon 6,6: It is prepared by the condensation polymerisation of hexamethylenediamine with adipic acid under high pressure and at high temperature.
(i) Nylon 6,6: It is prepared by the condensation polymerisation of hexamethylenediamine with adipic acid under high pressure and at high temperature.
Nylon 6, 6 is used in making sheets, bristles for brushes and in textile industry.
(ii) Nylon 6: It is obtained by heating caprolactum with water at a high temperature.
(ii) Nylon 6: It is obtained by heating caprolactum with water at a high temperature.
Nylon 6 is used for the manufacture of tyre cords, fabrics and ropes.
2. Polyesters
These are the polycondensation products of dicarboxylic acids and diols. Dacron or terylene is the best known example of polyesters. It is manufactured by heating a mixture of ethylene glycol and terephthalic acid at 420 to 460 K in the presence of zinc acetate antimony trioxide catalyst as per the reaction given earlier. Dacron fibre (terylene) is crease resistant and is used in blending with cotton and wool fibres and also as glass reinforcing materials in safety helmets, etc.
3. Phenol – formaldehyde polymer (Bakelite and related polymers)
Phenol – formaldehyde polymers are the oldest synthetic polymers. These are obtained by the condensation reaction of phenol with formaldehyde in the presence of either an acid or a base catalyst. The reaction starts with the initial formation of o-and/or p-hydroxymethylphenol derivatives, which further react with phenol
to form compounds having rings joined to each other through –CH2 groups. The initial product could be a linear product – Novolac used in paints.
Phenol – formaldehyde polymers are the oldest synthetic polymers. These are obtained by the condensation reaction of phenol with formaldehyde in the presence of either an acid or a base catalyst. The reaction starts with the initial formation of o-and/or p-hydroxymethylphenol derivatives, which further react with phenol
to form compounds having rings joined to each other through –CH2 groups. The initial product could be a linear product – Novolac used in paints.
Novolac on heating with formaldehyde undergoes cross linking to form an infusible solid mass called bakelite. It is used for making combs, phonograph records, electrical switches and handles of various utensils.
4. Melamine – formaldehyde polymer
Melamine formaldehyde polymer is formed by the condensation polymerisation of melamine and formaldehyde.
Melamine formaldehyde polymer is formed by the condensation polymerisation of melamine and formaldehyde.
It is used in the manufacture of unbreakable crockery.
Intext Question
15.3 Write the names of monomers of the following polymers:
15.4 Classify the following as addition and condensation polymers: Terylene, Bakelite, Polyvinyl chloride, Polythene.
15.3 Write the names of monomers of the following polymers:
15.4 Classify the following as addition and condensation polymers: Terylene, Bakelite, Polyvinyl chloride, Polythene.
15.2.3 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.
Copolymers have properties quite different from homopolymers. For example, butadiene – styrene copolymer is quite tough and is a good substitute for natural rubber. It is used for the manufacture of autotyres, floortiles, footwear components, cable insulation, etc.
15.2.4 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. This latex is obtained from the bark of rubber tree and is found in India, Srilanka, Indonesia, Malaysia and South America.
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. This latex is obtained from the bark of rubber tree and is found in India, Srilanka, Indonesia, Malaysia and South America.
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.
The cis-polyisoprene molecule consists of various chains held together by weak van der Waals interactions and has a coiled structure. Thus, it can be stretched like a spring and exhibits elastic properties.
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.
In the manufacture of tyre rubber, 5% of sulphur is used as a crosslinking agent. The probable structures of vulcanised rubber molecules are depicted below:
In the manufacture of tyre rubber, 5% of sulphur is used as a crosslinking agent. The probable structures of vulcanised rubber molecules are depicted below:
2. Synthetic rubbers
Synthetic rubber is any vulcanisable rubber like polymer, which is capable of getting stretched to twice its length. However, it returns to its original shape and size as soon as the external stretching force is released. Thus, synthetic rubbers are either homopolymers of 1, 3 – butadiene derivatives or copolymers of 1, 3 – butadiene or its derivatives with another unsaturated monomer.
Synthetic rubber is any vulcanisable rubber like polymer, which is capable of getting stretched to twice its length. However, it returns to its original shape and size as soon as the external stretching force is released. Thus, synthetic rubbers are either homopolymers of 1, 3 – butadiene derivatives or copolymers of 1, 3 – butadiene or its derivatives with another unsaturated monomer.
Preparation of Synthetic Rubbers
1. Neoprene
Neoprene or polychloroprene is formed by the free radical polymerisation of chloroprene.
1. Neoprene
Neoprene or polychloroprene is formed by the free radical polymerisation of chloroprene.
It has superior resistance to vegetable and mineral oils. It is used for manufacturing conveyor belts, gaskets and hoses.
2. Buna – N
You have already studied about Buna-S, in Section 15.1.3. Buna –N is obtained by the copolymerisation of 1, 3 – butadiene and acrylonitrile in the presence of a peroxide catalyst.
You have already studied about Buna-S, in Section 15.1.3. Buna –N is obtained by the copolymerisation of 1, 3 – butadiene and acrylonitrile in the presence of a peroxide catalyst.
It is resistant to the action of petrol, lubricating oil and organic solvents. It is used in making oil seals, tank lining, etc.
Intext Questions
15.5 Explain the difference between Buna-N and Buna-S.
15.6 Arrange the following polymers in increasing order of their intermolecular forces.
(i) Nylon 6,6, Buna-S, Polythene.
(ii) Nylon 6, Neoprene, Polyvinyl chloride.
15.5 Explain the difference between Buna-N and Buna-S.
15.6 Arrange the following polymers in increasing order of their intermolecular forces.
(i) Nylon 6,6, Buna-S, Polythene.
(ii) Nylon 6, Neoprene, Polyvinyl chloride.
15.3 Molecular Mass of Polymers
Polymer properties are closely related to their molecular mass, size and structure. The growth of the polymer chain during their synthesis is dependent upon the availability of the monomers in the reaction mixture. Thus, the polymer sample contains chains of varying lengths and hence its molecular mass is always expressed as an average. The molecular mass of polymers can be determined by chemical and physical methods.
15.4 Biodegradable Polymers
A large number of polymers are quite resistant to the environmental degradation processes and are thus responsible for the accumulation of polymeric solid waste materials. These solid wastes cause acute environmental problems and remain undegraded for quite a long time. In view of the general awareness and concern for the problems created by the polymeric solid wastes, certain new biodegradable synthetic polymers have been designed and developed. These polymers contain functional groups similar to the functional groups present in biopolymers.
Aliphatic polyesters are one of the important classes of biodegradable polymers. Some important examples are given below:
1. Poly β -hydroxybutyrate – co-β-hydroxy valerate (PHBV)
It is obtained by the copolymerisation of 3-hydroxybutanoic acid and 3 – hydroxypentanoic acid. PHBV is used in speciality packaging, orthopaedic devices and in controlled release of drugs. PHBV undergoes bacterial degradation in the environment.
Aliphatic polyesters are one of the important classes of biodegradable polymers. Some important examples are given below:
1. Poly β -hydroxybutyrate – co-β-hydroxy valerate (PHBV)
It is obtained by the copolymerisation of 3-hydroxybutanoic acid and 3 – hydroxypentanoic acid. PHBV is used in speciality packaging, orthopaedic devices and in controlled release of drugs. PHBV undergoes bacterial degradation in the environment.
2. Nylon 2–nylon 6
It is an alternating polyamide copolymer of glycine (H2N–CH2–COOH) and amino caproic acid [H2N(CH2)5COOH] and is biodegradable. Can you write the structure of this copolymer?
It is an alternating polyamide copolymer of glycine (H2N–CH2–COOH) and amino caproic acid [H2N(CH2)5COOH] and is biodegradable. Can you write the structure of this copolymer?
15.5 Polymers of Commercial Importance
Besides, the polymers already discussed, some other commercially important polymers along with their structures and uses are given below in Table 15.1.
Summary
Polymers are defined as high molecular mass macromolecules, which consist of repeating structural units derived from the corresponding monomers. These polymers may be of natural or synthetic origin and are classified in a number of ways.
In the presence of an organic peroxide initiator, the alkenes and their derivatives undergo addition polymerisation or chain growth polymerisation through a free radical mechanism. Polythene, teflon, orlon, etc. are formed by addition polymerisation of an appropriate alkene or its derivative. Condensation polymerisation reactions are shown by the interaction of bi – or poly functional monomers containing – NH2, – OH and – COOH groups. This type of polymerisation proceeds through the elimination of certain simple molecules as H2O, CH3OH, etc. Formaldehyde reacts with phenol and melamine to form the corresponding condensation polymer products. The condensation polymerisation progresses through step by step and is also called as step growth polymerisation. Nylon, bakelite and dacron are some of the important examples of condensation polymers. However, a mixture of two unsaturated monomers exhibits copolymerisation and forms a co-polymer containing multiple units of each monomer. Natural rubber is a cis 1, 4-polyisoprene and can be made more tough by the process of vulcanisation with sulphur. Synthetic rubbers are usually obtained by copolymerisation of alkene and 1, 3 butadiene derivatives.
In view of the potential environmental hazards of synthetic polymeric wastes, certain biodegradable polymers such as PHBV and Nylon-2- Nylon-6 are developed as alternatives.
In the presence of an organic peroxide initiator, the alkenes and their derivatives undergo addition polymerisation or chain growth polymerisation through a free radical mechanism. Polythene, teflon, orlon, etc. are formed by addition polymerisation of an appropriate alkene or its derivative. Condensation polymerisation reactions are shown by the interaction of bi – or poly functional monomers containing – NH2, – OH and – COOH groups. This type of polymerisation proceeds through the elimination of certain simple molecules as H2O, CH3OH, etc. Formaldehyde reacts with phenol and melamine to form the corresponding condensation polymer products. The condensation polymerisation progresses through step by step and is also called as step growth polymerisation. Nylon, bakelite and dacron are some of the important examples of condensation polymers. However, a mixture of two unsaturated monomers exhibits copolymerisation and forms a co-polymer containing multiple units of each monomer. Natural rubber is a cis 1, 4-polyisoprene and can be made more tough by the process of vulcanisation with sulphur. Synthetic rubbers are usually obtained by copolymerisation of alkene and 1, 3 butadiene derivatives.
In view of the potential environmental hazards of synthetic polymeric wastes, certain biodegradable polymers such as PHBV and Nylon-2- Nylon-6 are developed as alternatives.
Exercises
15.1 Explain the terms polymer and monomer.
15.1 Explain the terms polymer and monomer.
15.2 What are natural and synthetic polymers? Give two examples of each type.
15.3 Distinguish between the terms homopolymer and copolymer and give an example of each.
15.4 How do you explain the functionality of a monomer?
15.5 Define the term polymerisation.
15.6 Is ( NH-CHR-CO )n, a homopolymer or copolymer?
15.7 In which classes, the polymers are classified on the basis of molecular forces?
15.8 How can you differentiate between addition and condensation polymerisation?
15.9 Explain the term copolymerisation and give two examples.
15.10 Write the free radical mechanism for the polymerisation of ethene.
15.11 Define thermoplastics and thermosetting polymers with two examples of each.
15.12 Write the monomers used for getting the following polymers.
(i) Polyvinyl chloride (ii) Teflon (iii) Bakelite
(i) Polyvinyl chloride (ii) Teflon (iii) Bakelite
15.13 Write the name and structure of one of the common initiators used in free radical addition polymerisation.
15.14 How does the presence of double bonds in rubber molecules influence their structure and reactivity?
15.15 Discuss the main purpose of vulcanisation of rubber.
15.16 What are the monomeric repeating units of Nylon-6 and Nylon-6,6?
15.17 Write the names and structures of the monomers of the following polymers:
(i) Buna-S
(ii) Buna-N
(iii) Dacron
(iv) Neoprene
(i) Buna-S
(ii) Buna-N
(iii) Dacron
(iv) Neoprene
15.18 Identify the monomer in the following polymeric structures.
15.19 How is dacron obtained from ethylene glycol and terephthalic acid ?
15.20 What is a biodegradable polymer ? Give an example of a biodegradable aliphatic polyester.
Answers of Some Intext Questions
15.1 Polymers are high molecular mass substances consisting of large numbers of repeating structural units. They are also called as macromolecules. Some examples of polymers are polythene, bakelite, rubber, nylon 6, 6, etc.
15.2 On the basis of structure, the polymers are classified as below:
(i)Linear polymers such as polythene, polyvinyl chloride, etc.
(ii)Branched chain polymers such as low density polythene.
(iii)Cross linked polymers such as bakelite, melamine, etc.
(i)Linear polymers such as polythene, polyvinyl chloride, etc.
(ii)Branched chain polymers such as low density polythene.
(iii)Cross linked polymers such as bakelite, melamine, etc.
15.3(i) Hexamethylene diamine and adipic acid.
(ii) Caprolactam.
(iii) Tetrafluoroethene.
(ii) Caprolactam.
(iii) Tetrafluoroethene.
15.4 Addition polymers: Polyvinyl chloride, Polythene.
Condensation polymers: Terylene, Bakelite.
Condensation polymers: Terylene, Bakelite.
15.5 Buna-N is a copolymer of 1,3-butadiene and acrylonitrile and Buna-S is a copolymer of 1,3-butadiene and styrene.
15.6 In order of increasing intermolecular forces.
(i) Buna-S, Polythene, Nylon 6,6.
(ii) Neoprene, Polyvinyl chloride, Nylon 6.
15.6 In order of increasing intermolecular forces.
(i) Buna-S, Polythene, Nylon 6,6.
(ii) Neoprene, Polyvinyl chloride, Nylon 6.
I. Multiple Choice Questions (Type-I)
1. Which of the following polymers of glucose is stored by animals?
(i) Cellulose
(ii) Amylose
(iii) Amylopectin
(iv) Glycogen
(ii) Amylose
(iii) Amylopectin
(iv) Glycogen
2. Which of the following is not a semisynthetic polymer?
(i) cis-polyisoprene
(ii) Cellulose nitrate
(iii) Cellulose acetate
(iv) Vulcanised rubber
(ii) Cellulose nitrate
(iii) Cellulose acetate
(iv) Vulcanised rubber
3. The commercial name of polyacrylonitrile is ______________.
(i) Dacron
(ii) Orlon (acrilan)
(iii) PVC
(iv) Bakelite
(ii) Orlon (acrilan)
(iii) PVC
(iv) Bakelite
4. Which of the following polymer is biodegradable?
5. In which of the following polymers ethylene glycol is one of the monomer units?
6. Which of the following statements is not true about low density polythene?
(i) Tough
(ii) Hard
(iii) Poor conductor of electricity
(iv) Highly branched structure
(ii) Hard
(iii) Poor conductor of electricity
(iv) Highly branched structure
7.
is a polymer having monomer units ____________.
8. Which of the following polymer can be formed by using the following monomer unit?
(i) Nylon 6, 6
(ii) Nylon 2–nylon 6
(iii) Melamine polymer
(iv) Nylon-6
(ii) Nylon 2–nylon 6
(iii) Melamine polymer
(iv) Nylon-6
II. Multiple Choice Questions (Type-II)
Note : In the following questions two or more options may be correct.
9. Which of the following polymers, need atleast one diene monomer for their preparation?
(i) Dacron
(ii) Buna-S
(iii) Neoprene
(iv) Novolac
(ii) Buna-S
(iii) Neoprene
(iv) Novolac
10. Which of the folloiwng are characteristics of thermosetting polymers?
(i) Heavily branched cross linked polymers.
(ii) Linear slightly branched long chain molecules.
(iii) Become infusible on moulding so cannot be reused.
(iv) Soften on heating and harden on cooling, can be reused.
(ii) Linear slightly branched long chain molecules.
(iii) Become infusible on moulding so cannot be reused.
(iv) Soften on heating and harden on cooling, can be reused.
11. Which of the following polymers are thermoplastic?
(i) Teflon
(ii) Natural rubber
(iii) Neoprene
(iv) Polystyrene
(ii) Natural rubber
(iii) Neoprene
(iv) Polystyrene
12. Which of the following polymers are used as fibre?
(i) Polytetrafluoroethane
(ii) Polychloroprene
(iii) Nylon
(iv) Terylene
(ii) Polychloroprene
(iii) Nylon
(iv) Terylene
13. Which of the following are addition polymers?
(i) Nylon
(ii) Melamine formaldehyde resin
(iii) Orlon
(iv) Polystyrene
(ii) Melamine formaldehyde resin
(iii) Orlon
(iv) Polystyrene
14. Which of the following polymers are condensation polymers?
(i) Bakelite
(ii) Teflon
(iii) Butyl rubber
(iv) Melamine formaldehyde resin
(ii) Teflon
(iii) Butyl rubber
(iv) Melamine formaldehyde resin
15. Which of the following monomers form biodegradable polymers?
(i) 3-hydroxybutanoic acid + 3-hydroxypentanoic acid
(ii) Glycine + amino caproic acid
(iii) Ethylene glycol + phthalic acid
(iv) Caprolactum
(ii) Glycine + amino caproic acid
(iii) Ethylene glycol + phthalic acid
(iv) Caprolactum
16. Which of the following are example of synthetic rubber?
(i) Polychloroprene
(ii) Polyacrylonitrile
(iii) Buna-N
(iv) cis-polyisoprene
(ii) Polyacrylonitrile
(iii) Buna-N
(iv) cis-polyisoprene
17. Which of the following polymers can have strong intermolecular forces?
(i) Nylon
(ii) Polystyrene
(iii) Rubber
(iv) Polyesters
(ii) Polystyrene
(iii) Rubber
(iv) Polyesters
18. Which of the following polymers have vinylic monomer units?
(i) Acrilan
(ii) Polystyrene
(iii) Nylon
(iv) Teflon
(ii) Polystyrene
(iii) Nylon
(iv) Teflon
19. Vulcanisation makes rubber ______________.
(i) more elastic
(ii) soluble in inorganic solvent
(iii) crystalline
(iv) more stiff
(ii) soluble in inorganic solvent
(iii) crystalline
(iv) more stiff
III. Short Answer Type
20. A natural linear polymer of 2-methyl-1, 3-butadiene becomes hard on treatment with sulphur between 373 to 415 K and —S—S— bonds are formed between chains. Write the structure of the product of this treatment?
21. Identify the type of polymer.
—A—A—A—A—A—A—
—A—A—A—A—A—A—
22. Identify the type of polymer.
—A—B—B—A—A—A—B—A—
—A—B—B—A—A—A—B—A—
23. Out of chain growth polymerisation and step growth polymerisation, in which type will you place the following.
24. Identify the type of polymer given in the following figure.
25. Identify the polymer given below :
26. Why are rubbers called elastomers?
27. Can enzyme be called a polymer?
28. Can nucleic acids, proteins and starch be considered as step growth polymers?
29. How is the following resin intermediate prepared and which polymer is formed by this monomer unit?
27. Can enzyme be called a polymer?
28. Can nucleic acids, proteins and starch be considered as step growth polymers?
29. How is the following resin intermediate prepared and which polymer is formed by this monomer unit?
30. To have practical applications why are cross links required in rubber?
31. Why does cis-polyisoprene possess elastic property?
31. Why does cis-polyisoprene possess elastic property?
32. What is the structural difference between HDP and LDP? How does the structure account for different behaviour and nature, hence the use of a polymer?
33. What is the role of benzoyl peroxide in addition polymerisation of alkenes? Explain its mode of action with the help of an example.
34. Which factor imparts crystalline nature to a polymer like nylon?
35. Name the polymers used in laminated sheets and give the name of monomeric units involved in its formation.
36. Which type of biomolecules have some structural similarity with synthetic polyamides? What is this similarity?
37. Why should the monomers used in addition polymerisation through free radical pathway be very pure?
33. What is the role of benzoyl peroxide in addition polymerisation of alkenes? Explain its mode of action with the help of an example.
34. Which factor imparts crystalline nature to a polymer like nylon?
35. Name the polymers used in laminated sheets and give the name of monomeric units involved in its formation.
36. Which type of biomolecules have some structural similarity with synthetic polyamides? What is this similarity?
37. Why should the monomers used in addition polymerisation through free radical pathway be very pure?
IV. Matching Type
Note : Match the items of Column I with the items in Column II.
38. Match the polymer of column I with correct monomer of column II.
| Column I | Column II | ||
| (i) | High density polythene | (a) | Isoprene |
| (ii) | Neoprene | (b) | Tetrafluoroethene |
| (iii) | Natural rubber | (c) | Chloroprene |
| (iv) | Teflon | (d) | Acrylonitrile |
| (v) | Acrilan | (e) | Ethene |
39. Match the polymers given in Column I with their chemical names given in Column II.
| Column I | Column II | ||
| (i) | Nylon 6 | (a) | Polyvinyl chloride |
| (ii) | PVC | (b) | Polyacrylonitrile |
| (iii) | Acrilan | (c) | Polycaprolactum |
| (iv) | Natural rubber | (d) | Low density polythene |
| (v) | LDP | (e) | cis-polyisoprene |
40. Match the polymers given in Column I with their commercial names given in Column II.
| Column I | Column II | ||
| (i) | Polyester of glycol and phthalic acid | (a) | Novolac |
| (ii) | Copolymer of 1, 3-butadiene and styrene | (b) | Glyptal |
| (iii) | Phenol and formaldehyde resin | (c) | Buna-S |
| (iv) | Polyester of glycol and terephthalic acid | (d) | Buna-N |
| (v) | Copolymer of 1, 3-butadiene and acrylonitrile | (e) | Dacron |
41. Match the polymers given in Column I with their main applications given in Column II.
| Column I | Column II | ||
| (i) | Bakelite | (a) | Unbreakable crockery |
| (ii) | Low density polythene | (b) | Non-stick cookwares |
| (iii) | Melamine-formaldehyde resin | (c) | Packaging material for shock absorbance |
| (iv) | Nylon 6 | (d) | Electrical switches |
| (v) | Polytetrafluoroethane | (e) | Squeeze bottles |
| (vi) | Polystyrene | (f) | Tyre, cords |
42. Match the polymers given in Column I with the preferred mode of polymerisation followed by their monomers.
| Column I | Column II | ||
| (i) | Nylon-6,6 | (a) | Free radical polymerisation |
| (ii) | PVC | (b) | Ziegler-Natta polymerisation or coordination polymerisation |
| (iii) | HDP | (c) | Anionic polymerisation |
| (d) | Condensation polymerisation |
43. Match the polymers given in Column I with the type of linkage present in
them given in Column II.
them given in Column II.
| Column I | Column II | ||
| (i) | Terylene | (a) | Glycosidic linkage |
| (ii) | Nylon | (b) | Ester linkage |
| (iii) | Cellulose | (c) | Phosphodiester linkage |
| (iv) | Protein | (d) | Amide linkage |
| (v) | RNA |
44. Match materials given in Column I with the polymers given in Column II.
| Column I | Column II | ||
| (i) | Natural rubber latex | (a) | Nylon |
| (ii) | Wood laminates | (b) | Neoprene |
| (iii) | Ropes and fibres | (c) | Dacron |
| (iv) | Polyester fabric | (d) | Melamine formaldehyde resins |
| (v) | Synthetic rubber | (e) | Urea-formaldehyde resins |
| (vi) | Unbreakable crockery | (f) | cis-polyisoprene |
45. Match the polymers given in Column I with their repeating units given in Column II.
V. Assertion and Reason Type
Note : In the following questions a statement of assertion followed by a statement of reason is given. Choose the correct answer out of the following choices.
(i) Assertion and reason both are correct statement but reason does not explain assertion.
(ii) Assertion and reason both are correct statements and reason explains the assertion.
(iii) Both assertion and reason are wrong statement.
(iv) Assertion is correct statement and reason is wrong statement.
(v) Assertion is wrong statement and reason is correct statement.
(ii) Assertion and reason both are correct statements and reason explains the assertion.
(iii) Both assertion and reason are wrong statement.
(iv) Assertion is correct statement and reason is wrong statement.
(v) Assertion is wrong statement and reason is correct statement.
46. Assertion : Rayon is a semi synthetic polymer and is taken as a better choice than cotton fabric.
Reason : Mechanical and aesthetic properties of cellulose can be improved by acetylation.
Reason : Mechanical and aesthetic properties of cellulose can be improved by acetylation.
47. Assertion : Most of the Synthetic polymers are not biodegradable.
Reason : Polymerisation process induces toxic character in organic molecules.
Reason : Polymerisation process induces toxic character in organic molecules.
48. Assertion : Olefinic monomers undergo addition polymerisation.
Reason : Polymerisation of vinylchloride is initiated by peroxides/persulphates.
Reason : Polymerisation of vinylchloride is initiated by peroxides/persulphates.
49. Assertion : Polyamides are best used as fibres because of high tensile strength.
Reason : Strong intermolecular forces (like hydrogen bonding within polyamides) lead to close packing of chains and increase the crystalline character, hence, provide high tensile strength to polymers.
Reason : Strong intermolecular forces (like hydrogen bonding within polyamides) lead to close packing of chains and increase the crystalline character, hence, provide high tensile strength to polymers.
50. Assertion : For making rubber synthetically, isoprene molecules are polymerised.
Reason : Neoprene (a polymer of chloroprene) is a synthetic rubber.
Reason : Neoprene (a polymer of chloroprene) is a synthetic rubber.
51. Assertion : Network polymers are thermosetting.
Reason : Network polymers have high molecular mass.
Reason : Network polymers have high molecular mass.
52. Assertion : Polytetrafluoroethene is used in making non-stick cookwares.
Reason : Fluorine has highest electronegativity.
Reason : Fluorine has highest electronegativity.
VI. Long Answer Type
53. Synthetic polymers do not degrade in the environment for a long time. How can biodegradable synthetic polymers be made. Differentiate between biopolymers and biodegradable polymers and give examples of each type.
54. Differentiate between rubbers and plastics on the basis of intermolecular forces.
55. Phenol and formaldehyde undergo condensation to give a polymar (A) which on heating with formaldehyde gives a thermosetting polymer (B). Name the polymers. Write the reactions involved in the formation of (A). What is the
structural difference between two polymers?
structural difference between two polymers?
56. Low density polythene and high density polythene, both are polymers of ethene but there is marked difference in their properties. Explain.
57. Which of the following polymers soften on heating and harden on cooling? What are the polymers with this property collectively called? What are the structural similarities between such polymers? Bakelite, urea-formaldehyde resin, polythene, polyvinyls, polystyrene.
ANSWERS
I. Multiple Choice Questions (Type-I)
1. (iv) 2. (i) 3. (ii) 4. (iv) 5. (i) 6. (iii) 7. (i) 8. (iv)
II. Multiple Choice Questions (Type-II)
9. (ii), (iii) 10. (i), (iii) 11. (i), (iv) 12. (iii), (iv) 13. (iii), (iv) 14. (i), (iv)
15. (i), (ii) 16. (i), (iii) 17. (i), (iv) 18. (i), (ii), (iv) 19. (i), (iv)
15. (i), (ii) 16. (i), (iii) 17. (i), (iv) 18. (i), (ii), (iv) 19. (i), (iv)
III. Short Answer Type
20. Vulcanised rubber. For structure see Class XII NCERT textbook.
21. Homopolymer
22. Copolymer
23. Chain growth polymerisation
24. Cross-linked polymer
25. Polyisoprene/Natural rubber
26. Rubbers are stretched on application of force and regain original state after the force is removed. Therefore these are called elastomers.
27. Enzymes are biocatalysts which are proteins and are thus polymers.
28. [Hint : Yes, step growth polymers are condensation polymers and they are formed by the loss of simple molecule like water leading to the formation of high molecular mass polymers.]
29. Melamine and formaldehyde are starting materials for this intermediate. Its polymerisation gives melamine polymer.
30. Cross links bind the planar polymer sheets thus increasing its elastomeric properties.
31. See Class XII, NCERT text book, page no.434.
32. See Class-XII NCERT textbook, page no. 429-30.
33. See Class-XII NCERT textbook, page no. 428.
34. Strong intermolecular forces like hydrogen-bonding, lead to close packing of chains that imparts crystalline character.
35. Urea formaldehyde resins. Monomer units are urea and formaldehyde.
21. Homopolymer
22. Copolymer
23. Chain growth polymerisation
24. Cross-linked polymer
25. Polyisoprene/Natural rubber
26. Rubbers are stretched on application of force and regain original state after the force is removed. Therefore these are called elastomers.
27. Enzymes are biocatalysts which are proteins and are thus polymers.
28. [Hint : Yes, step growth polymers are condensation polymers and they are formed by the loss of simple molecule like water leading to the formation of high molecular mass polymers.]
29. Melamine and formaldehyde are starting materials for this intermediate. Its polymerisation gives melamine polymer.
30. Cross links bind the planar polymer sheets thus increasing its elastomeric properties.
31. See Class XII, NCERT text book, page no.434.
32. See Class-XII NCERT textbook, page no. 429-30.
33. See Class-XII NCERT textbook, page no. 428.
34. Strong intermolecular forces like hydrogen-bonding, lead to close packing of chains that imparts crystalline character.
35. Urea formaldehyde resins. Monomer units are urea and formaldehyde.
36. Proteins. Polyamides and proteins both contain amide linkage.
37. Pure monomers are required because even the traces of impurities may act like inhibitors which leads to the formation of polymers with shorter chain length.
37. Pure monomers are required because even the traces of impurities may act like inhibitors which leads to the formation of polymers with shorter chain length.
IV. Matching Type
38. (i) → (e) (ii) → (c) (iii) → (a) (iv) → (b) (v) → (d)
39. (i) → (c) (ii) → (a) (iii) → (b) (iv) → (e) (v) → (d)
40. (i) → (b) (ii) → (c) (iii) → (a) (iv) → (e) (v) → (d)
41. (i) → (d) (ii) → (e) (iii) → (a) (iv) → (f) (v) → (b) (vi) → (c)
42. (i) → (d) (ii) → (a) (iii) → (b)
43. (i) → (b) (ii) → (d) (iii) → (a) (iv) → (d) (v) → (c)
44. (i) → (f) (ii) → (e) (iii) → (a) (iv) → (c) (v) → (b) (vi) → (d)
45. (i) → (d) (ii) → (a) (iii) → (b) (iv) → (e) (v) → (c)
39. (i) → (c) (ii) → (a) (iii) → (b) (iv) → (e) (v) → (d)
40. (i) → (b) (ii) → (c) (iii) → (a) (iv) → (e) (v) → (d)
41. (i) → (d) (ii) → (e) (iii) → (a) (iv) → (f) (v) → (b) (vi) → (c)
42. (i) → (d) (ii) → (a) (iii) → (b)
43. (i) → (b) (ii) → (d) (iii) → (a) (iv) → (d) (v) → (c)
44. (i) → (f) (ii) → (e) (iii) → (a) (iv) → (c) (v) → (b) (vi) → (d)
45. (i) → (d) (ii) → (a) (iii) → (b) (iv) → (e) (v) → (c)
V. Assertion and Reason Type
46. (ii) 47. (iv) 48. (i) 49. (ii) 50. (v) 51. (i) 52. (i)
1 comment:
Excellent blog sir.
But i wanted to know if dacron and glyptal are the same.
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