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  A polymer is a substance composed of molecules with large molecular mass composed of repeating structural units, or monomers, connected by covalent chemical bonds. The word is derived from the Greek, πολυ, polu, "many"; and μέρος, meros, "part". Well known examples of polymers include plastics, DNA and proteins.

While the term polymer in popular usage suggests "plastic", polymers comprise a large class of natural and synthetic materials with a variety of properties and purposes. Natural polymer materials such as shellac and amber have been in use for centuries. Biopolymers such as proteins (for example hair, skin and part of the bone structure) and nucleic acids play crucial roles in biological processes. A variety of other natural polymers exist, such as cellulose, which is the main constituent of wood and paper.


Historical development

Starting in 1811 Henri Braconnot did pioneering work in derivative cellulose compounds, perhaps the earliest important work in polymer science. The term polymer was coined in 1833 by Jöns Jakob Berzelius. The development of vulcanization later in the nineteenth century improved the durability of the natural polymer rubber, signifying the first popularized semi-synthetic polymer. The first wholly synthetic polymer, Bakelite, was introduced in 1909.

Despite significant advances in synthesis and characterization of polymers, a proper understanding of polymer molecular structure did not come until the 1920s. Before that, scientists believed that polymers were clusters of small molecules (called colloids), without definite molecular weights, held together by an unknown force, a concept known as association theory. In 1922, Hermann Staudinger proposed that polymers consisted of long chains of atoms held together by covalent bonds, an idea which did not gain wide acceptance for over a decade, and for which Staudinger was ultimately awarded the Nobel Prize. An important contribution to synthetic polymer science was given by the Italian chemist Giulio Natta and Karl Ziegler who won the Nobel Prize in Chemistry in 1963 for the development of the Ziegler-Natta catalyst. In the intervening century, synthetic polymer materials such as Nylon, polyethylene, Teflon, and silicone have formed the basis for a burgeoning polymer industry.

Synthetic polymers today find application in nearly every industry and area of life. Polymers are widely used as adhesives and lubricants, as well as structural components for products ranging from children's toys to aircraft. Polymers such as poly (methyl methacrylate) find application as photoresist materials used in semiconductor manufacturing and low-k dielectrics for use in high-performance microprocessors. Future applications include flexible polymer-based substrates for electronic displays and improved time-released and targeted drug delivery.

Polymer science

Main article: Polymer science

Most polymer research may be classified as polymer science, a sub-discipline of materials science which includes researchers in chemistry (especially organic chemistry), physics, and engineering. Polymer science may be roughly divided into two subdisciplines:

  • Polymer chemistry or macromolecular chemistry, concerned with the chemical synthesis and chemical properties of polymers.
  • Polymer physics, concerned with the bulk properties of polymer materials and engineering applications.

The field of polymer science is generally concerned with synthetic polymers, such as plastics, or chemical treatment and modification of natural polymers.

The study of biological polymers, their structure, function, and method of synthesis is generally the purview of biology, biochemistry, and biophysics. These disciplines share some of the terminology familiar to polymer science, especially when describing the synthesis of biopolymers such as DNA or polysaccharides. However, usage differences persist, such as the practice of using the term macromolecule to describe large non-polymer molecules and complexes of multiple molecular components, such as hemoglobin. Substances with distinct biological function are rarely described in the terminology of polymer science. For example, a protein is rarely referred to as a copolymer.

Organic synthesis

Main article: Polymerization

In 1907, Leo Baekeland created the first completely synthetic polymer, Bakelite, by reacting phenol and formaldehyde at precisely controlled temperature and pressure. Subsequent work by Wallace Carothers in the 1920s demonstrated that polymers could be synthesized rationally from their constituent monomers. The intervening years have shown significant developments in rational polymer synthesis. Most commercially important polymers today are entirely synthetic and produced in high volume, on appropriately scaled organic synthetic techniques.

Laboratory synthetic methods are generally divided into two categories, condensation polymerization and addition polymerization. However, some newer methods such as plasma polymerization do not fit neatly into either category. Synthetic polymerization reactions may be carried out with or without a catalyst. Efforts towards rational synthesis of biopolymers via laboratory synthetic methods, especially artificial synthesis of proteins, is an area of intense research.

Biological synthesis

Main article: Biopolymer

There are three main classes of biopolymers: polysaccharides, polypeptides, and polynucleotides. In living cells they may be synthesized by enzyme-mediated processes, such as the formation of DNA catalyzed by DNA polymerase. The synthesis of proteins involves multiple enzyme-mediated processes to transcribe genetic information from the DNA and subsequently translate that information to synthesize the specified protein from amino acids. The protein may be modified further following translation in order to provide appropriate structure and function.

Modification of natural polymers

Many commercially important polymers are synthesized by chemical modification of naturally occurring polymers. Prominent examples include the reaction of nitric acid and cellulose to form nitrocellulose and the formation of vulcanized rubber by heating natural rubber in the presence of sulfur

Polymer Structure and Properties

Types of polymer 'properties' can be broadly divided into several categories based upon scale. At the nano-micro scale are properties that directly describe the chain itself. These can be thought of as polymer structure. At an intermediate mesoscopic level are properties that describe the morphology of the polymer matrix in space. At the macroscopic level are properties that describe the bulk behavior of the polymer.


The structural properties of a polymer relate to the physical arrangement of monomers along the backbone of the chain. Structure has a strong influence on the other properties of a polymer. For example, a linear chain polymer may be soluble or insoluble in water depending on whether it is composed of polar monomers (such as ethylene oxide) or nonpolar monomers (such as styrene). On the other hand, two samples of natural rubber may exhibit different durability even though their molecules comprise the same monomers. Polymer scientists have developed terminology to precisely describe both the nature of the monomers as well as their relative arrangement:

Monomer identity

The identity of the monomers comprising the polymer is generally the first and most important attribute of a polymer. Polymer nomenclature is generally based upon the type of monomers comprising the polymer. Polymers that contain only a single type of monomer are known as homopolymers, while polymers containing a mixture of monomers are known as copolymers. Poly(styrene), for example, is composed only of styrene monomers, and is therefore is classified as a homopolymer. Ethylene-vinyl acetate, on the other hand, contains more than one variety of monomer and is thus a copolymer. Some biological polymers are composed of a variety of different but structurally related monomers, such as polynucleotides composed of nucleotide subunits.

A polymer molecule containing ionizable subunits is known as a polyelectrolyte. An ionomer is a subclass of polyelectrolyte with a low fraction of ionizable subunits.

Chain linearity

The simplest form of polymer molecule is a straight chain or linear polymer, composed of a single main chain. The flexibility of an unbranched chain polymer is characterized by its persistence length. A branched polymer molecule is composed of a main chain with one or more substituent side chains or branches. Special types of branched polymers include star polymers, comb polymers, and brush polymers. If the polymer contains a side chain that has a different composition or configuration than the main chain, the polymer is called a graft or grafted polymer. A cross-link suggests a branch point from which four or more distinct chains emanate. A polymer molecule with a high degree of crosslinking is referred to as a polymer network.[1] Sufficiently high crosslink concentrations may lead to the formation of an 'infinite network', also known as a 'gel', in which networks of chains are of unlimited extend - there is essentially all chains have linked into one molecule.[2]

Chain size

Polymer bulk properties may be strongly dependent on the size of the polymer chain. Like any molecule, a polymer molecule's size may be described in terms of molecular weight or mass. In polymers, however, the molecular mass may be expressed in terms of degree of polymerization, essentially the number of monomer units which comprise the polymer. For synthetic polymers, the molecular weight is expressed statistically to describe the distribution of molecular weights in the sample. This is because of the fact that almost all industrial processes produce a distribution of polymer chain sizes. Examples of such statistics include the number average molecular weight and weight average molecular weight. The ratio of these two values is the polydispersity index, commonly used to express the "width" of the molecular weight.

The space occupied by a polymer molecule is generally expressed in terms of radius of gyration or excluded volume.

Monomer arrangement in copolymers

Main article: copolymer

Monomers within a copolymer may be organized along the backbone in a variety of ways.

  • Alternating copolymers possess regularly alternating monomer residues
  • Periodic copolymers have monomer residue types arranged in a repeating sequence
  • Random copolymers have a random sequence of monomer residue types
  • Statistical copolymers have monomer residues arranged according to a known statistical rule
  • Block copolymers have two or more homopolymer subunits linked by covalent bonds. Block copolymers with two or three distinct blocks are called diblock copolymers and triblock copolymers, respectively.

Tacticity in polymers with chiral centers

Main article: Tacticity

This property describes the relative stereochemistry of chiral centers in neighboring structural units within a macromolecule. There are three types: isotactic, atactic, and syndiotactic.

Morphological Properties


When applied to polymers, the term crystalline has a somewhat ambiguous usage. In some cases, the term crystalline finds identical usage to that used in conventional crystallography. For example, the structure of a crystalline protein or polynucleotide, such as a sample prepared for x-ray crystallography, may be defined in terms of a conventional unit cell composed of one or more polymer molecules with cell dimensions of hundreds of angstroms or more.

A synthetic polymer may be described as crystalline if it contains regions of three-dimensional ordering on atomic (rather than macromolecular) length scales, usually arising from intramolecular folding and/or stacking of adjacent chains. Synthetic polymers may consist of both crystalline and amorphous regions; the degree of crystallinity may be expressed in terms of a weight fraction or volume fraction of crystalline material. Few synthetic polymers are entirely crystalline.[3]

Bulk properties

The bulk properties of a polymer are those most often of end-use interest. These are the properties that dictate how the polymer actually behaves on a macroscopic scale.

Tensile strength

The tensile strength of a material quantifies how much stress the material will endure before failing. This is very important in applications that rely upon polymer's physical strength or durability. For example, a rubber band with a higher tensile strength will hold a greater weight before snapping. In general tensile strength increases with polymer chain length.

Young's Modulus of elasticity

Young's Modulus quantifies the elasticity of the polymer. It is defined, for small strains, as the ratio of rate of change of stress to strain. Like tensile strength this is highly relevant in polymer applications involving the physical properties of polymers, such as rubber bands.

Transport Properties

Transport properties such as diffusivity relate to how rapidly molecules move through the polymer matrix. These are very important in many applications of polymers for films and membranes.

Pure component phase behavior

Melting point

The term "melting point" when applied to polymers suggests not a solid-liquid phase transition but a transition from a crystalline or semi-crystalline phase to a solid amorphous phase. Though abbreviated as simply "Tm", the property in question is more properly called the "crystalline melting temperature". Among synthetic polymers, crystalline melting is only discussed with regards to thermoplastics, as thermosetting polymers will decompose at high temperatures rather than melt.

Boiling point

The boiling point of a polymer substance is never defined due to the fact that polymers will decompose before reaching theoretical boiling temperatures.

Glass transition temperature (Tg)

A parameter of particular interest in synthetic polymer manufacturing is the glass transition temperature (Tg), which describes the temperature at which amorphous polymers undergo a second order phase transition from a rubbery, viscous amorphous solid to a brittle, glassy amorphous solid. The glass transition temperature may be engineered by altering the degree of branching or cross-linking in the polymer or by the addition of plasticizer.[4]

In general, polymeric mixtures are far less miscible than mixtures of small molecule materials. This effect is a result of the fact that the driving force for mixing is usually entropics, not energetics. In other words, miscible materials usually form a solution not because their interaction with each other is more favorable than their self-interaction but because of an increase in entropy and hence free energy associated with increasing the amount of volume available to each component. This increase in entropy scales with the number of particles (or moles) being mixed. Since polymeric molecules are much larger and hence generally have much higher specific volumes than small molecules, the number of molecules involved in a polymeric mixture are far less than the number in a small molecule mixture of equal volume. The energetics of mixing, on the other hand, are comparable on a per volume basis for polymeric and small molecule mixtures. This tends to increase the free energy of mixing for polymer solutions and thus make solvation less favorable. Thus, concentrated solutions of polymers are far rarer than those of small molecules.

In dilute solution, the properties of the polymer are characterized by the interaction between the solvent and the polymer. In a good solvent, the polymer appears swollen and occupies a large volume. In this scenario, intermolecular forces between the solvent and monomer subunits dominate over intramolecular interactions. In a bad solvent or poor solvent, intramolecular forces dominate and the chain contracts. In the theta solvent, or the state of the polymer solution where the value of the second virial coefficient becomes 0, the intermolecular polymer-solvent repulsion balances exactly the intramolecular monomer-monomer attraction. Under the theta condition (also called the Flory condition) the polymer behaves like an ideal random coil.

Polymer Structure/Property relationships

Polymer bulk properties are strongly dependent upon their structure and mesoscopic behavior. A number of qualitative relationships between structure and properties are known.

Chain length

Increasing chain length tends to decrease chain mobility, increase strength and toughness, and increase the glass transition temperature (Tg). This is a result of the increase in chain interactions such as Van der Waals attractions and entanglements that come with increased chain length. These interactions tend to fix the individual chains more strongly in position and resist deformations and matrix breakup, both at higher stresses and higher temperatures. Chain length is related to melt viscosity roughly as 1:103.2, so that a tenfold increase in polymer chain length results in a viscosity increase of over 1000 times.


Branching of polymer chains also affect the bulk properties of polymers. Long chain branches may increase polymer strength, toughness, and Tg due to an increase in the number of entanglements per chain. Random length and atactic short chains, on the other hand, may reduce polymer strength due to disruption of organization. Short side chains may likewise reduce crystallinity due to disruption of the crystal structure. Reduced crystallinity may also be associated with increased transparency due to light scattering by small crystalline regions. A good example of this effect is related to the range of physical attributes of polyethylene. High density polyethylene (HDPE) has a very low degree of branching, is quite stiff, and is used in applications such as milk jugs. Low density polyethylene (LDPE), on the other hand, has significant numbers of short branches, is quite flexible, and is used in applications such as plastic films. The branching index of the polymer is a parameter that characterizes the effect of long-chain branches on the size of a branched macromolecule in solution.

Chemical cross-linking

Cross linking tends to increase Tg and increase strength and toughness. Cross linking consists of the formation of chemical bonds between chains. Among other applications, this process is used to strengthen rubbers in a process known as vulcanization, which is based on cross linking by sulfur. Car tires, for example, are highly cross linked in order to reduce the leaking of air out of the tire and to toughen their durability. Eraser rubber, on the other hand, is not cross linked to allow flaking of the rubber and prevent damage to the paper.

Inclusion of plasticizers

Inclusion of plasticizers tends to lower Tg and increase polymer flexibility. Plasticizers are generally small molecules that are chemically similar to the polymer and create gaps between polymer chains for greater mobility and reduced interchain interactions. A good example of the action of plasticizers is related to polyvinylchlorides or PVCs. A uPVC or unplastiscized polyvinylchloride is used for things such as pipes. A pipe has no plasticizers in it because it needs to remain strong and heat resistant. Plasticized PVC is used for clothing for a flexible quality. Plasticizers are also put in some types of cling film to make the polymer more flexible.

Degree of crystallinity

Increasing degree of crystallinity tends to make a polymer more rigid. It can also lead to greater brittlness. Polymers with degree of crystallinity approaching zero or one will tend to be transparent, while polymers with intermediate degrees of crystallinity will tend to be opaque due to light scattering by crystalline / glassy regions.

Standardized polymer nomenclature

There are multiple conventions for naming polymer substances. Many commonly used polymers, such as those found in consumer products, are referred to by a common or trivial name. The trivial name is assigned based on historical precedent or popular usage rather than a standardized naming convention. Both the American Chemical Society[5] and IUPAC[6] have proposed standardized naming conventions; the ACS and IUPAC conventions are similar but not identical.[7] Examples of the difference between the various naming conventions are given in the table below:

Common Name ACS Name IUPAC Name
Poly (ethylene oxide) or (PEO) poly(oxyethylene) poly(oxyethylene)
Poly (ethylene terephthalate) or (PET) poly (oxy-1,2-ethanediyloxycarbonyl -1,4-phenylenecarbonyl) poly (oxyethyleneoxyterephth= aloyl)
Nylon poly[imino(1-oxo-1,6-hexanediyl)] poly[imino(1-oxohexane-1,6-diyl)]

In both standardized conventions the polymers names are intended to reflect the monomer(s) from which they are synthesized rather than the precise nature of the repeating subunit. For example, the polymer synthesized from the simple alkene ethene is called polyethylene, retaining the -ene suffix even though the double bond is removed during the polymerization process:

Chemical properties of polymers

The attractive forces between polymer chains play a large part in determining a polymer's properties. Because polymer chains are so long, these interchain forces are amplified far beyond the attractions between conventional molecules. Different side groups on the polymer can lend the polymer to ionic bonding or hydrogen bonding between its own chains. These stronger forces typically result in higher tensile strength and melting points.

The intermolecular forces in polymers can be affected by dipoles in the monomer units. Polymers containing amide or carbonyl groups can form hydrogen bonds between adjacent chains; the partially positively charged hydrogen atoms in N-H groups of one chain are strongly attracted to the partially negatively charged oxygen atoms in C=O groups on another. These strong hydrogen bonds, for example, result in the high tensile strength and melting point of polymers containing urethane or urea linkages. Polyesters have dipole-dipole bonding between the oxygen atoms in C=O groups and the hydrogen atoms in H-C groups. Dipole bonding is not as strong as hydrogen bonding, so a polyester's melting point and strength are lower than Kevlar's (Twaron), but polyesters have greater flexibility.

Ethene, however, has no permanent dipole. The attractive forces between polyethylene chains arise from weak van der Waals forces. Molecules can be thought of as being surrounded by a cloud of negative electrons. As two polymer chains approach, their electron clouds repel one another. This has the effect of lowering the electron density on one side of a polymer chain, creating a slight positive dipole on this side. This charge is enough to actually attract the second polymer chain. Van der Waals forces are quite weak, however, so polyethene can have a lower melting temperature compared to other polymers.

Polymer characterization

The characterization of a polymer requires several parameters which need to be specified. This is because a polymer actually consists of a statistical distribution of chains of varying lengths, and each chain consists of monomer residues which affect its properties.

A variety of lab techniques are used to determine the properties of polymers. Techniques such as wide angle X-ray scattering, small angle X-ray scattering, and small angle neutron scattering are used to determine the crystalline structure of polymers. Gel permeation chromatography is used to determine the number average molecular weight, weight average molecular weight, and polydispersity. FTIR, Raman and NMR can be used to determine composition. Thermal properties such as the glass transition temperature and melting point can be determined by differential scanning calorimetry and dynamic mechanical analysis. Pyrolysis followed by analysis of the fragments is one more technique for determining the possible structure of the polymer.

Polymer degradation

Polymer degradation is a change in the properties - tensile strength, colour, shape, etc - of a polymer or polymer based product under the influence of one or more environmental factors such as heat, light or chemicals. It is often due to the hydrolysis of the bonds connecting the polymer chain, which in turn leads to a decrease in the molecular mass of the polymer. These changes may be undesirable, such as changes during use, or desirable, as in biodegradation or deliberately lowering the molecular mass of a polymer. Such changes occur primarily because of the effect of these factors on the chemical composition of the polymer.

The degradation of polymers to form smaller molecules may proceed by random scission or specific scission. The degradation of polyethylene occurs by random scission - that is by a random breakage of the linkages (bonds) that hold the atoms of the polymer together. When heated above 450 Celsius it degrades to form a mixture of hydrocarbons. Other polymers - like polyalphamethylstyrene - undergo 'specific' chain scission with breakage occurring only at the ends. They literally unzip or depolymerize to become the constituent monomer. Cracking refers to thermally or otherwise degrading the polymer to recover either monomers or oligomers.

In a finished product such a change is to be prevented or delayed. However the degradation process can be useful from the view points of understanding the structure of a polymer or recycling/reusing the polymer waste to prevent or reduce environmental pollution. Polylactic acid and Polyglycolic acid, for example, are two polymers that are useful for their ability to degrade under aqueous conditions. A copolymer of these polymers is used for biomedical applications such as hydrolysable stitches that degrade over time after they are applied to a wound. These materials can also be used for plastics that will degrade over time after they are used and will therefore not remain as litter.

Today there are primarily six commodity polymers in use, namely polyethylene, polypropylene, polyvinyl chloride, polyethylene terephthalate, polystyrene and polycarbonate. Each of these polymers has its own characteristic modes of degradation and resistances to heat, light and chemicals.


  1. ^ IUPAC. "Glossary of Basic Terms in Polymer Science". Pure Appl. Chem. 1996, 68, 2287-2311.
  2. ^ Painter, P and Coleman, M. "Fundamentals of Polymer Science". 1997, 96-100.
  3. ^
  4. ^ Brandrup, J.; Immergut, E.H.; Grulke, E.A.; eds Polymer Handbook 4th Ed. New York: Wiley-Interscience, 1999.
  5. ^ CAS: Index Guide, Appendix IV (© 1998).
  6. ^ IUPAC. "Nomenclature of Regular Single-Strand Organic Polymers". Pure Appl. Chem. 1976, 48, 373-385.
  7. ^ [1]
  • Ashby, Michael and Jones, David. Engineering Materials. p. 191-195. Oxford: Butterworth-Heinermann, 1996. Ed. 2.
  • Meyers and Chawla. Mechanical Behavior of Materials. pg. 41. Prentice Hall, Inc. 1999.

See also

This article is licensed under the GNU Free Documentation License. It uses material from the Wikipedia article "Polymer". A list of authors is available in Wikipedia.
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