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Polymerization

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Title: Polymerization  
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Polymerization

An example of alkene polymerization, in which each styrene monomer's double bond reforms as a single bond plus a bond to another styrene monomer. The product is polystyrene.
IUPAC definition

polymerization: The process of converting a monomer or a mixture of monomers into a polymer. [1]

In [4] There are many forms of polymerization and different systems exist to categorize them.

Contents

  • Introduction 1
  • Step-growth 2
  • Chain-growth 3
    • Physical polymer reaction engineering 3.1
    • Photopolymerization 3.2
  • See also 4
  • References 5

Introduction

Homopolymers
A + A + A... \rightarrow AAA ...
Copolymers
A + B + A... \rightarrow ABA ...

In chemical compounds, polymerization occurs via a variety of reaction mechanisms that vary in complexity due to [4]

As alkenes can be formed in somewhat straightforward reaction mechanisms, they form useful compounds such as [4] due to their usefulness in manufacturing processes of commercial products, such as piping, insulation and packaging. In general, polymers such as PVC are referred to as "homopolymers," as they consist of repeated long chains or structures of the same monomer unit, whereas polymers that consist of more than one molecule are referred to as copolymers (or co-polymers).[5]

Other monomer units, such as formaldehyde hydrates or simple aldehydes, are able to polymerize themselves at quite low temperatures (ca. −80 °C) to form [4] in smaller molecules. Generally, because formaldehyde is an exceptionally reactive electrophile it allows nucleophillic addition of hemiacetal intermediates, which are in general short-lived and relatively unstable "mid-stage" compounds that react with other molecules present to form more stable polymeric compounds.

Polymerization that is not sufficiently moderated and proceeds at a fast rate can be very hazardous. This phenomenon is known as hazardous polymerization and can cause fires and explosions.

Step-growth

Step-growth polymers are defined as polymers formed by the stepwise reaction between functional groups of monomers, usually containing heteroatoms such as nitrogen or oxygen. Most step-growth polymers are also classified as condensation polymers, but not all step-growth polymers (like polyurethanes formed from isocyanate and alcohol bifunctional monomers) release condensates; in this case, we talk about addition polymers. Step-growth polymers increase in molecular weight at a very slow rate at lower conversions and reach moderately high molecular weights only at very high conversion (i.e., >95%).

To alleviate inconsistencies in these naming methods, adjusted definitions for condensation and addition polymers have been developed. A condensation polymer is defined as a polymer that involves loss of small molecules during its synthesis, or contains heteroatoms as part of its backbone chain, or its repeat unit does not contain all the atoms present in the hypothetical monomer to which it can be degraded.

Chain-growth

Chain-growth polymerization (or addition polymerization) involves the linking together of molecules incorporating double or triple carbon-carbon bonds. These unsaturated monomers (the identical molecules that make up the polymers) have extra internal bonds that are able to break and link up with other monomers to form a repeating chain, whose backbone typically contains only carbon atoms. Chain-growth polymerization is involved in the manufacture of polymers such as polyethylene, polypropylene, and polyvinyl chloride (PVC). A special case of chain-growth polymerization leads to living polymerization.

In the radical polymerization of ethylene, its π bond is broken, and the two electrons rearrange to create a new propagating center like the one that attacked it. The form this propagating center takes depends on the specific type of addition mechanism. There are several mechanisms through which this can be initiated. The free radical mechanism is one of the first methods to be used. Free radicals are very reactive atoms or molecules that have unpaired electrons. Taking the polymerization of ethylene as an example, the free radical mechanism can be divided into three stages: chain initiation, chain propagation, and chain termination.

Polymerization of ethylene

Free radical addition polymerization of ethylene must take place at high temperatures and pressures, approximately 300 °C and 2000 atm. While most other free radical polymerizations do not require such extreme temperatures and pressures, they do tend to lack control. One effect of this lack of control is a high degree of branching. Also, as termination occurs randomly, when two chains collide, it is impossible to control the length of individual chains. A newer method of polymerization similar to free radical, but allowing more control involves the Ziegler-Natta catalyst, especially with respect to polymer branching.

Other forms of chain growth polymerization include cationic addition polymerization and anionic addition polymerization. While not used to a large extent in industry yet due to stringent reaction conditions such as lack of water and oxygen, these methods provide ways to polymerize some monomers that cannot be polymerized by free radical methods such as polypropylene. Cationic and anionic mechanisms are also more ideally suited for living polymerizations, although free radical living polymerizations have also been developed.

Esters of acrylic acid contain a carbon-carbon double bond which is conjugated to an ester group. This allows the possibility of both types of polymerization mechanism. An acrylic ester by itself can undergo chain-growth polymerization to form a homopolymer with a carbon-carbon backbone, such as poly(methyl methacrylate). Also, however, certain acrylic esters can react with diamine monomers by nucleophilic conjugate addition of amine groups to acrylic C=C bonds. In this case the polymerization proceeds by step-growth and the products are poly(beta-amino ester) copolymers, with backbones containing nitrogen (as amine) and oxygen (as ester) as well as carbon.[6]

Physical polymer reaction engineering

To produce a high-molecular-weight, uniform product, various methods are employed to better control the initiation, propagation, and termination rates during chain polymerization and also to remove excess concentrated heat during these exothermic reactions compared to polymerization of the pure monomer. These include emulsion polymerization, solution polymerization, suspension polymerization, and precipitation polymerization. Although the polymer polydispersity and molecular weight may be improved, these methods may introduce additional processing requirements to isolate the product from a solvent.

Photopolymerization

Photopolymerization reactions are chain-growth polymerizations which are initiated by the absorption of visible or ultraviolet light. The light may be absorbed either directly by the reactant monomer (direct photopolymerization), or else by a photosensitizer which absorbs the light and then transfers energy to the monomer. In general only the initiation step differs from that of the ordinary thermal polymerization of the same monomer; subsequent propagation, termination and chain transfer steps are unchanged.[7]

Photopolymerization can be used as a photographic or printing process, because polymerization only occurs in regions which have been exposed to light. Unreacted monomer can be removed from unexposed regions, leaving a relief polymeric image.[7] Several forms of 3D printing -- including layer-by-layer stereolithography and two-photon absorption 3D photopolymerization -- use photopolymerization.

See also

References

  1. ^ Jenkins, A. D.; Kratochvíl, P.; Stepto, R. F. T.; Suter, U. W. (1996). "Glossary of basic terms in polymer science (IUPAC Recommendations 1996)".   See definition 3.1, p. 2305.
  2. ^ Young, R. J. (1987) Introduction to Polymers, Chapman & Hall ISBN 0-412-22170-5
  3. ^ Polymerization, IUPAC Gold Book (2000) et al.International Union of Pure and Applied Chemistry,
  4. ^ a b c d e f g h Clayden, J., Greeves, N. and Warren, S. (2000). Organic chemistry, Oxford University Press ISBN 0198503466 pp. 1450–1466
  5. ^ Cowie, J.M.G. (1991) Polymers: Chemistry and Physics of Modern Materials, Chapman and Hall, p. 4 ISBN 0849398134
  6. ^ Lynn, David M.; Langer, Robert (2000). "Degradable Poly(β-amino esters):  Synthesis, Characterization, and Self-Assembly with Plasmid DNA". Journal of the American Chemical Society 122 (44): 10761.  
  7. ^ a b Allcock H.R., Lampe F.W. and Mark J.F. Contemporary Polymer Chemistry (3rd ed. Pearson Prentice-Hall 2003), chap.5. ISBN 0-13-065056-0
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