Difference between revisions of "Polymer"

Latest revision as of 09:11, 20 September 2010

A polymer is a large molecule (macromolecule) composed of repeating structural units typically connected by covalent chemical bonds. While polymer in popular usage suggests plastic, the term actually refers to a large class of natural and synthetic materials with a wide variety of properties.

Because of the extraordinary range of properties of polymeric materials,^[2] they play an essential and ubiquitous role in everyday life^[3], ranging from familiar synthetic plastics and elastomers to natural biopolymers such as DNA and proteins that are essential for life. A simple example is polyethylene, whose repeating unit is based on ethylene (IUPAC name ethene) monomer. Most commonly, as in this example, the continuously linked backbone of a polymer used for the preparation of plastics consists mainly of carbon atoms. However, other structures do exist; for example, elements such as silicon form familiar materials such as silicones, examples being silly putty and waterproof plumbing sealant. The backbone of DNA is in fact based on a phosphodiester bond, and repeating units of polysaccharides (e.g. cellulose) are joined together by glycosidic bonds via oxygen atoms.

Natural polymeric materials such as shellac, amber, and natural rubber have been used for centuries. Biopolymers such as proteins 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.

The list of synthetic polymers includes synthetic rubber, Bakelite, neoprene, nylon, PVC, polystyrene, polyethylene, polypropylene, polyacrylonitrile, PVB, silicone, and many more.

Polymers are studied in the fields of polymer chemistry, polymer physics, and polymer science.

Etymology

The word polymer is derived from the Greek words πολυ- - poly- meaning "many"; and μέρος - meros meaning "part". The term was coined in 1833 by Jöns Jacob Berzelius, although his definition of a polymer was quite different from the modern definition. (see New chemical terms)

Historical development

Starting in 1811, Henri Braconnot did pioneering work in derivative cellulose compounds, perhaps the earliest important work in polymer science. The development of vulcanization later in the nineteenth century improved the durability of the natural polymer rubber, signifying the first popularized semi-synthetic polymer. In 1907, Leo Baekeland created the first completely synthetic polymer, Bakelite, by reacting phenol and formaldehyde at precisely controlled temperature and pressure. Bakelite was then publicly introduced in 1909.

Despite significant advances in synthesis and characterization of polymers, a correct understanding of polymer molecular structure did not emerge until the 1920s. Before then, 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. Work by Wallace Carothers in the 1920s also demonstrated that polymers could be synthesized rationally from their constituent monomers. An important contribution to synthetic polymer science was made by the Italian chemist Giulio Natta and the German chemist Karl Ziegler, who won the Nobel Prize in Chemistry in 1963 for the development of the Ziegler-Natta catalyst. Further recognition of the importance of polymers came with the award of the Nobel Prize in Chemistry in 1974 to Paul Flory, whose extensive work on polymers included the kinetics of step-growth polymerization and of addition polymerization, chain transfer, excluded volume, the Flory-Huggins solution theory, and the Flory convention.

Synthetic polymer materials such as nylon, polyethylene, Teflon, and silicone have formed the basis for a burgeoning polymer industry. These years have also 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. 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. They have been employed in a variety of biomedical applications ranging from implantable devices to controlled drug delivery. 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. Recently, polymers have also been employed as flexible substrates in the development of organic light-emitting diodes for electronic display.

Polymer synthesis

Polymerization is the process of combining many small molecules known as monomers into a covalently bonded chain. During the polymerization process, some chemical groups may be lost from each monomer. This is the case, for example, in the polymerization of PET polyester. The monomers are terephthalic acid (HOOC-C₆H₄-COOH) and ethylene glycol (HO-CH₂-CH₂-OH) but the repeating unit is -OC-C₆H₄-COO-CH₂-CH₂-O-, which corresponds to the combination of the two monomers with the loss of two water molecules. The distinct piece of each monomer that is incorporated into the polymer is known as a repeat unit or monomer residue.

Laboratory synthesis

Laboratory synthetic methods are generally divided into two categories, step-growth polymerization and chain-growth polymerization^[4]. The essential difference between the two is that in chain growth polymerization, monomers are added to the chain one at a time only^[5], whereas in step-growth polymerization chains of monomers may combine with one another directly^[6]. 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. Laboratory synthesis of biopolymers, especially of proteins, is an area of intensive research.

Biological synthesis

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 to RNA 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 functioning.

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 properties

Polymer properties are broadly divided into several classes based on the scale at which the property is defined as well as upon its physical basis^[7]. The most basic property of a polymer is the identity of its constituent monomers. A second set of properties, known as microstructure, essentially describe the arrangement of these monomers within the polymer at the scale of a single chain. These basic structural properties play a major role in determining bulk physical properties of the polymer, which describe how the polymer behaves as a continuous macroscopic material. Chemical properties, at the nano-scale, describe how the chains interact through various physical forces. At the macro-scale, they describe how the bulk polymer interacts with other chemicals and solvents.

Monomers and repeat units

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

A polymer molecule containing ionizable subunits is known as a polyelectrolyte or ionomer.

Microstructure

The microstructure of a polymer (sometimes called configuration) relates to the physical arrangement of monomer residues along the backbone of the chain^[8]. These are the elements of polymer structure that require the breaking of a covalent bond in order to change. Structure has a strong influence on the other properties of a polymer. For example, two samples of natural rubber may exhibit different durability, even though their molecules comprise the same monomers.

Polymer architecture

An important microstructural feature determining polymer properties is the polymer architecture.^[9] The simplest polymer architecture is a linear chain: a single backbone with no branches. A related unbranching architecture is a ring polymer. 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, brush polymers, dendronized polymers, ladders, and dendrimers^[9].

Branching of polymer chains affects the ability of chains to slide past one another by altering intermolecular forces, in turn affecting bulk physical polymer properties. Long chain branches may increase polymer strength, toughness, and the glass transition temperature (T_g) due to an increase in the number of entanglements per chain. The effect of such long-chain branches on the size of the polymer in solution is characterized by the branching index. Random length and atactic short chains, on the other hand, may reduce polymer strength due to disruption of organization and may likewise reduce the crystallinity of the polymer.

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 both long and short branches, is quite flexible, and is used in applications such as plastic films.

Dendrimers are a special case of polymer where every monomer unit is branched. This tends to reduce intermolecular chain entanglement and crystallization. Alternatively, dendritic polymers are not perfectly branched but share similar properties to dendrimers due to their high degree of branching.

The architecture of the polymer is often physically determined by the functionality of the monomers from which it is formed^[10]. This property of a monomer is defined as the number of reaction sites at which may form chemical covalent bonds. The basic functionality required for forming even a linear chain is two bonding sites. Higher functionality yields branched or even crosslinked or networked polymer chains.

An effect related to branching is chemical crosslinking - the formation of covalent bonds between chains. Crosslinking tends to increase T_g and increase strength and toughness. Among other applications, this process is used to strengthen rubbers in a process known as vulcanization, which is based on crosslinking by sulfur. Car tires, for example, are highly crosslinked 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 crosslinked to allow flaking of the rubber and prevent damage to the paper.

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.^[11] 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 extent—essentially all chains have linked into one molecule.^[12]

Chain length

The physical properties^[13] of a polymer are strongly dependent on the size or length of the polymer chain.^[14]. For example, as chain length is increased, melting and boiling temperatures increase quickly^[14]. Impact resistance also tends to increase with chain length, as does the viscosity, or resistance to flow, of the polymer in its melt state^[15]. Chain length is related to melt viscosity roughly as 1:10^3.2, so that a tenfold increase in polymer chain length results in a viscosity increase of over 1000 times^{[citation needed]}. Increasing chain length furthermore tends to decrease chain mobility, increase strength and toughness, and increase the glass transition temperature (T_g)^{[citation needed]}. This is a result of the increase in chain interactions such as Van der Waals attractions and entanglements that come with increased chain length^{[citation needed]}. 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^{[citation needed]}.

A common means of expressing the length of a chain is the degree of polymerization, which quantifies the number of monomers incorporated into the chain^[16][17]. As with other molecules, a polymer's size may also be expressed in terms of molecular weight. Since synthetic polymerization techniques typically yield a polymer product including a range of molecular weights, the weight is often expressed statistically to describe the distribution of chain lengths present in the same. Common examples are the number average molecular weight and weight average molecular weight^[18][19]. The ratio of these two values is the polydispersity index, commonly used to express the "width" of the molecular weight distribution.^[20] A final measurement is contour length, which can be understood as the length of the chain backbone in its fully extended state^[21].

The flexibility of an unbranched chain polymer is characterized by its persistence length.

Monomer arrangement in copolymers

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

• Alternating copolymers possess regularly alternating monomer residues:^[22] [AB...]_n (2).
• Periodic copolymers have monomer residue types arranged in a repeating sequence: [A_nB_m...] m being different from n .
• Statistical copolymers have monomer residues arranged according to a known statistical rule. A statistical copolymer in which the probability of finding a particular type of monomer residue at an particular point in the chain is independent of the types of surrounding monomer residue may be referred to as a truly random copolymer^[23][24] (3).
• Block copolymers have two or more homopolymer subunits linked by covalent bonds^[22] (4). Polymers with two or three blocks of two distinct chemical species (e.g., A and B) are called diblock copolymers and triblock copolymers, respectively. Polymers with three blocks, each of a different chemical species (e.g., A, B, and C) are termed triblock terpolymers.
• Graft or grafted copolymers contain side chains that have a different composition or configuration than the main chain.(5)

Tacticity

Tacticity describes the relative stereochemistry of chiral centers in neighboring structural units within a macromolecule. There are three types: isotactic (all substituents on the same side), atactic (random placement of substituents), and syndiotactic (alternating placement of substituents).

Polymer morphology

Polymer morphology generally describes the arrangement of chains in space and microscopic ordering of many polymer chains.

Crystallinity

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 lightly 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.^[25]

The crystallinity of polymers is characterized by their degree of crystallinity, ranging from zero for a completely non-crystalline polymer to one for a theoretical completely crystalline polymer. Polymers with microcrystalline regions are generally tougher (can be bent more without breaking) and more impact-resistant than totally amorphous polymers.^[26]

Polymers with a 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 or glassy regions. Thus for many polymers, reduced crystallinity may also be associated with increased transparency.

Chain conformation

The space occupied by a polymer molecule is generally expressed in terms of radius of gyration, which is an average distance from the center of mass of the chain to the chain itself. Alternatively, it may be expressed in terms of pervaded volume, which is the volume of solution spanned by the polymer chain and scales with the cube of the radius of gyration.^[27]

Mechanical properties

The bulk properties of a polymer are those most often of end-use interest. These are the properties that indictate 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 suffering permanent deformation.^[28][29] This is very important in applications that rely upon a 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 and crosslinking of polymer chains.

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. The modulus is strongly dependent on temperature.

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.

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 T_m, 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 polymeric material is strongly dependent on chain length. High polymers with a large degree of polymerization do not exhibit a boiling point because they decompose before reaching theoretical boiling temperatures. For shorter oligomers, a boiling transition may be observed and will generally increase rapidly as chain length is increased.

Glass transition temperature

A parameter of particular interest in synthetic polymer manufacturing is the glass transition temperature (T_g), which describes the temperature at which amorphous polymers undergo a second-order phase transition from a rubbery, viscous amorphous solid, or from a crystalline solid (depending on the degree of crystallization) to a brittle, glassy amorphous solid. The glass transition temperature may be engineered by altering the degree of branching or crosslinking in the polymer or by the addition of plasticizer.^[30]

Mixing behavior

In general, polymeric mixtures are far less miscible than mixtures of small molecule materials. This effect results from the fact that the driving force for mixing is usually entropy, not interaction energy. 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 is far smaller than the number in a small molecule mixture of equal volume. The energetics of mixing, on the other hand, is 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.

Furthermore, the phase behavior of polymer solutions and mixtures is more complex than that of small molecule mixtures. Whereas most small molecule solutions exhibit only an upper critical solution temperature phase transition, at which phase separation occurs with cooling, polymer mixtures commonly exhibit a lower critical solution temperature phase transition, at which phase separation occurs with heating.

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.

Inclusion of plasticizers

Inclusion of plasticizers tends to lower T_g 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 unplasticized 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.

Chemical properties

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 higher crystalline 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 attract the second polymer chain. Van der Waals forces are quite weak, however, so polyethylene can have a lower melting temperature compared to other polymers.

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^[31] and IUPAC^[32] have proposed standardized naming conventions; the ACS and IUPAC conventions are similar but not identical.^[33] Examples of the differences between the various naming conventions are given in the table below:

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:

File:Ethene polymerization.png

File:Polyethene monomer.png

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. Thermogravimetry is a useful technique to evaluate the thermal stability of the polymer. Detailed analyses of TG curves also allow us to know a bit of the phase segregation in polymers. Rheological properties are also commonly used to help determine molecular architecture (molecular weight, molecular weight distribution and branching)as well as to understand how the polymer will process, through measurements of the polymer in the melt phase. Another Polymer characterization technique is Automatic Continuous Online Monitoring of Polymerization Reactions (ACOMP) which provides real-time characterization of polymerization reactions. It can be used as an analytical method in R&D, as a tool for reaction optimization at the bench and pilot plant level and, eventually, for feedback control of full-scale reactors. ACOMP measures in a model-independent fashion the evolution of average molar mass and intrinsic viscosity, monomer conversion kinetics and, in the case of copolymers, also the average composition drift and distribution. It is applicable in the areas of free radical and controlled radical homo- and copolymerization, polyelectrolyte synthesis, heterogeneous phase reactions, including emulsion polymerization, adaptation to batch and continuous reactors, and modifications of polymers.^[34][35][36]

Polymer degradation

Polymer degradation is a change in the properties—tensile strength, color, shape, molecular weight, etc.—of a polymer or polymer-based product under the influence of one or more environmental factors, such as heat, light, chemicals and, in some cases, galvanic action. 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. Ozone cracking and UV degradation are specific failure modes for certain polymers. The susceptibility of a polymer to degradation depends on its structure. Epoxies and chains containing aromatic functionality are especially susceptible to UV degradation while polyesters are susceptible to degradation by hydrolysis. Carbon based polymers are more susceptible to thermal degradation than inorganically bound polymers such as Polydimethylsiloxane and are therefore not ideal for most high temperature applications.

Polymer degradation may occur through galvanic action similar to that of metals. In 1990, Michael Faudree discovered that imide-linked resins in CFRP (carbon fiber reinforced polymers) composites degrade when bare composite is coupled with an active metal in saline, i.e. salt water environments.^[37][38]Polymers affected include bismaleimides (BMI), condensation polyimides, triazines, and blends thereof. Degradation occurs in the form of dissolved resin and loose fibers. Hydroxyl ions are generated at the graphite cathode attacking the O-C-N bond in the polyimide structure. This phenomenon, that polymers can undergo galvanic corrosion like metals do has been referred to as the "Faudree Effect". Standard corrosion protection procedures were found to prevent polymer degradation under most conditions.

The degradation of polymers to form smaller molecules may proceed by random scission or specific scission. The degradation of polyethylene occurs by random scission—a random breakage of the linkages (bonds) that hold the atoms of the polymer together. When heated above 450 °C 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.

However, the degradation process can be useful from the viewpoints 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.

The sorting of polymer waste for recycling purposes may be facilitated by the use of the Resin identification codes developed by the Society of the Plastics Industry to identify the type of plastic.

Product failure

In a finished product, such a change is to be prevented or delayed. Failure of safety-critical polymer components can cause serious accidents, such as fire in the case of cracked and degraded polymer fuel lines. Chlorine-induced cracking of acetal resin plumbing joints and polybutylene pipes has caused many serious floods in domestic properties, especially in the USA in the 1990s. Traces of chlorine in the water supply attacked vulnerable polymers in the plastic plumbing, a problem which occurs faster if any of the parts have been poorly extruded or injection molded. Attack of the acetal joint occurred because of faulty molding, leading to cracking along the threads of the fitting which is a serious stress concentration.

Polymer oxidation has caused accidents involving medical devices. One of the oldest known failure modes is ozone cracking caused by chain scission when ozone gas attacks susceptible elastomers such as natural rubber and nitrile rubber. They possess double bonds in their repeat units which are cleaved during ozonolysis. Cracks in fuel lines can penetrate the bore of the tube and cause fuel leakage. If cracking occurs in the engine compartment, electric sparks can ignite the gasoline and can cause a serious fire.

Fuel lines can also be attacked by another form of degradation: hydrolysis. Nylon 6,6 is susceptible to acid hydrolysis, and in one accident, a fractured fuel line led to a spillage of diesel into the road. If diesel fuel leaks onto the road, accidents to following cars can be caused by the slippery nature of the deposit, which is like black ice.

See also

References

Bibliography

• Cowie, J.M.G. Polymers: Chemistry and Physics of Modern Materials, Blackie (in USA: Chapman and Hall), 2nd edition (1991).
• Ezrin, Meyer. Plastics Failure Guide: Cause and Prevention, Hanser-SPE (1996).
• Lewis, Peter Rhys; Reynolds, K.; and Gagg, C. Forensic Materials Engineering: Case studies, CRC Press (2004).
• McCrum N. G., Buckley C. P., Bucknall C. B., Principles of Polymer Engineering, Oxford University Press, 1997 ISBN 978-0-19-856526-0
• Painter P. C., Coleman M. M., Fundamentals of Polymer Science: an Introductory Text, CRC Press, 1997 ISBN 1-56676-559-5
• Rubinstein, M. and Colby, R., Polymer Physics, Oxford University Press, 2006 ISBN 0-19-852059-X
• Sperling L. H., Introduction to Physical Polymer Science, Wiley & Sons, 2006 ISBN 0-471-70606-X
• Wright, David C. Environmental Stress Cracking of Plastics, RAPRA (2001).
• Lewis, Peter Rhys, and Gagg, C, Forensic Polymer Engineering: Why polymer products fail in service, Woodhead/CRC Press (2010).
• Workman, J. Handbook of Organic Compounds: NIR, IR, Raman, and UV-VIS Spectra Featuring Polymers, and Surfactants (3 Volumes), Academic Press (2000) ISBN-13: 9780127635606.

External links

• How To Identify the Polymer
• Polymer Chemistry Hypertext, Educational resource
• The Macrogalleria
• Application notes on the characterization of polymers
• Distance learning course in polymers
• Polymer Structures
• Glossary of Polymer Abbreviations
• Sigma-Aldrich Polymer Glossaryar:مكوثر

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1. ↑ Y. Roiter and S. Minko (2005). "AFM Single Molecule Experiments at the Solid-Liquid Interface: In Situ Conformation of Adsorbed Flexible Polyelectrolyte Chains". Journal of the American Chemical Society. 127 (45): 15688–15689. doi:10.1021/ja0558239. PMID 16277495. 
2. ↑ Painter, p. 1
3. ↑ McCrum, p. 1
4. ↑ Sperling, p. 10
5. ↑ Sperling, p. 11
6. ↑ Sperling, p. 15
7. ↑ S.A. Baeurle (2009). "Multiscale modeling of polymer materials using field-theoretic methodologies: a survey about recent developments". Journal of Mathematical Chemistry. 46 (2): 363–426. doi:10.1007/s10910-008-9467-3. 
8. ↑ Sperling, p. 30
9. ↑ ^{9.0 9.1} Rubinstein, p. 6
10. ↑ Lua error in package.lua at line 80: module 'Module:Citation/CS1/Suggestions' not found.
11. ↑ IUPAC; Kratochvíl, P.; Stepto, R. F. T.; Suter, U. W. (1996). "Glossary of Basic Terms in Polymer Science". Pure Appl. Chem. 68: 2287–2311. doi:10.1351/pac199668122287. 
12. ↑ Painter, pp. 96-100
13. ↑ De Gennes, P.-G., Scaling Concepts in Polymer Physics, Cornell University Press, 1979
14. ↑ ^{14.0 14.1} Rubinstein, p. 5
15. ↑ McCrum, p. 37
16. ↑ McCrum, p. 30
17. ↑ Rubinstein, p. 3
18. ↑ McCrum, p. 33
19. ↑ Rubinstein, pp. 23-24
20. ↑ Painter, p. 22
21. ↑ Rubinstein, p. 50
22. ↑ ^{22.0 22.1} Painter, p. 14
23. ↑ Painter, p. 15
24. ↑ Sperling, p. 47
25. ↑ "IUPAC Purple Book: Definition of terms relating to crystalline polymers (1988) See Sec.1.3 Degree of Crystallinity" (PDF). 
26. ↑ Allcock, Harry R.; Lampe, Frederick W.; and Mark, James E. (2003). Contemporary Polymer Chemistry (3 ed.). Pearson Education. p. 546. ISBN 0130650560. CS1 maint: Multiple names: authors list (link)
27. ↑ Rubinstein, p. 13
28. ↑ Ashby, Michael and Jones, David (1996). Engineering Materials (2 ed.). Butterworth-Heinermann. pp. 191–195. ISBN 0750627662. CS1 maint: Multiple names: authors list (link)
29. ↑ M. A. Meyers and K. K. Chawla (1999). Mechanical Behavior of Materials. Cambridge University Press. p. 41. ISBN 978-0-521-86675-0. 
30. ↑ Brandrup, J.; Immergut, E.H.; Grulke, E.A. (1999). Polymer Handbook (4 ed.). Wiley-Interscience. ISBN 0471479365. CS1 maint: Multiple names: authors list (link)
31. ↑ CAS: Index Guide, Appendix IV ((c) 1998)
32. ↑ IUPAC (1976). "Nomenclature of Regular Single-Strand Organic Polymers". Pure Appl. Chem. 48: 373–385. doi:10.1351/pac197648030373. 
33. ↑ "Macromolecular Nomenclature Note No. 18". 
34. ↑ U.S. Patent 6,052,184 and U.S. Patent 6,653,150, other patents pending
35. ↑ F. H. Florenzano; R. Strelitzki; W. F. Reed (1998). "Absolute, Online Monitoring of Polymerization Reactions". Macromolecules. 31 (21): 7226–7238. doi:10.1021/ma980876e. CS1 maint: Multiple names: authors list (link)
36. ↑ A. M. Alb; M. F. Drenski; W. F. Reed (2008). "Implications to Industry: Perspective. Automatic continuous online monitoring of polymerization reactions (ACOMP)". Polymer International. 57: 390–396. doi:10.1002/pi.2367. CS1 maint: Multiple names: authors list (link)
37. ↑ Faudree M.C., Relationship of Graphite/Polyimide Composites to Galvanic Processes (1991). Society for the Advancement of Material and Process Engineering (SAMPE) Journal. 2: 1288–1301.  Missing or empty |title= (help)
38. ↑ Faudree M.C. and Fujimaki A. (2004) Basic English for Science and Technology, (3rd printing) Eihosha, Tokyo. ISBN 4-269-18019-6 C1082