Polyformaldehyde

Polyacetaldehyde, a mbbery polymer with an acetal stmcture, was first discovered in 1936 (49,50). More recentiy, it has been shown that a white, nontacky, and highly elastic polymer can be formed by cationic polymerization using BF in Hquid ethylene (51). At temperatures below —75° C using anionic initiators, such as metal alkyls in a hydrocarbon solvent, a crystalline, isotactic polymer is obtained (52). This polymer also has an acetal [poly(oxymethylene)] stmcture. Molecular weights in the range of 800,000—3,000,000 have been reported. Polyacetaldehyde is unstable and depolymerizes in a few days to acetaldehyde. The methods used for stabilizing polyformaldehyde have not been successful with poly acetaldehyde and the polymer has no practical significance (see Acetalresins). 

Acetal Resins. Acetal resins (qv) are poly (methylene oxide) or polyformaldehyde homopolymers and formaldehyde [50-00-0] copolymeri2ed with ahphatic oxides such as ethylene oxide (42). The homopolymer resin polyoxymethylene [9002-81-7] (POM) is produced by the anionic catalytic polymeri2ation of formaldehyde. For thermal stabiUty, the resin is endcapped with an acyl or alkyl function. 

In the above examples the polymerisation takes place by the opening of a carbon-carbon double bond. It is also possible to open carbonyl carbon-oxygen double bonds and nitrile carbon-nitrogen triple bonds. An example of the former is the polymerisation of formaldehyde to give polyformaldehyde (also known as polyoxymethylene and polyacetal) (Figure 2.3). 

By deactivating the active weak link. For example, commercial polyacetal (polyformaldehyde) resins have their chain ends capped by a stable grouping. (This will, however, be of little use where the initiation of chain degradation is not at the terminal group.)... 

Some polymers such as the polyacetals (polyformaldehyde) and poly(methyl methacrylate) depolymerise to monomer on heating. At processing temperatures such monomers are in the gaseous phase and even where there is only a small amount of depolymerisation a large number of bubbles can be formed in the products. 

Besides being commercially referred to as polyacetal materials polyformaldehydes are also often known as polyoxymethylenes and are the simplest type of a family of aliphatic polyethers. 

In order to manufacture such polymers, it is first necessary to produce a very pure form of formaldehyde. This is typieally produced from an alkali-precipitated low molecular weight polyformaldehyde which has been carefuly washed with distilled water and dried for several hours under vacuum at about 80°C. The dried polymer is then pyrolysed by heating at 150-160°C, and the resultant formaldehyde passed through a number of cold traps (typically four) at -15°C. Some prepolymerisation occurs in these traps and removes undesirable... 

Polymers produced by methods as described above have thermal stabilities many times greater than those obtained by the earlier bulk and solution methods of Staudinger. Staudinger had, however, shown that the diacetates of low molecular weight polyoxymethylenes (I) (polyformaldehydes) were more stable than the simple polyoxymethylene glycols (II) (Figure 19.2). 

Chemical Designations - Synonyms Fonnaldehyde polymer Polyformaldehyde Polyfooxymethylene Polyoxymethylene glycol Chemical Formula HO(CHjO) H. 

Poly(ethylene terephtlhalate) Phenol-formaldehyde Polyimide Polyisobutylene Poly(methyl methacrylate), acrylic Poly-4-methylpentene-1 Polyoxymethylene polyformaldehyde, acetal Polypropylene Polyphenylene ether Polyphenylene oxide Poly(phenylene sulphide) Poly(phenylene sulphone) Polystyrene Polysulfone Polytetrafluoroethylene Polyurethane Poly(vinyl acetate) Poly(vinyl alcohol) Poly(vinyl butyral) Poly(vinyl chloride) Poly(vinylidene chloride) Poly(vinylidene fluoride) Poly(vinyl formal) Polyvinylcarbazole Styrene Acrylonitrile Styrene butadiene rubber Styrene-butadiene-styrene Urea-formaldehyde Unsaturated polyester... 

Thermoplastic Resins and Molding Compounds Group 1. Acetal Resins Acetal, linear (Polyformaldehyde) >10 6,5 1.9 113 4,100 440 0,020 0.035 C11... 

In other instances the reactions appear to occur in sequence down the chain, for example in the depolymerisation reaction of polyformaldehyde (polyacetal) and polymethyl methacrylate which are referred to as zippering or sometimes unzippering reactions. In other cases cyclisation reactions can occur such as on heating polyacrylonitrile ... 

Polyformaldehydes (polyoxymethylenes, polyacetals) These are physically similar to general purpose nylons but with greater stiffness and lower water absorption. There are no solvents, but swelling occurs in liquids of similar solubility parameter. Poor resistance to u.v. light and limited thermal stability are two disadvantages of these materials. 

Specific ordn using polyethers, such as Polysaccharides and Polyurethanes, are entered separately below. Polyethers already entered include Polyformaldehyde in Vol 6, F164-L to F167-L and Epoxy Resins in Vol 5, E106-R to E107-L ... 

Solid phase polymerisation is used for chain polymerisation processes which are carried out at low temperatures. In such processes the thermal activation is difficult and so for activation of such processes radiation-activation technique is used. These processes are very slow. An example of such a solid phase polymerisation is the preparation of Polyformaldehyde by the radiation polymerisation of solid trioxane. 

Polyformaldehyde is made up of CH2 0 repeat units and can be produced by the cationic polymerisation of either formaldehyde or trioxane. 

Uses Solvent for nitrocellulose, ethyl cellulose, polyvinyl butyral, rosin, shellac, manila resin, dyes fuel for utility plants home heating oil extender preparation of methyl esters, formaldehyde, methacrylates, methylamines, dimethyl terephthalate, polyformaldehydes methyl halides, ethylene glycol in gasoline and diesel oil antifreezes octane booster in gasoline source of hydrocarbon for fuel cells extractant for animal and vegetable oils denaturant for ethanol in formaldehyde solutions to inhibit polymerization softening agent for certain plastics dehydrator for natural gas intermediate in production of methyl terLbutyl ether. 

The industrial synthesis of polyformaldehyde [poly(oxymethylene)] occurs by anionic polymerization of formaldehyde in suspension. For this the purification and handling of monomeric formaldehyde is of special importance since it tends to form solid paraformaldehyde. After the polymerization the semiacetal end groups have to be protected in order to avoid thermal depolymerization (Example 5-13). This is achieved by esterfication with acetic anhydride (see Example 5-7). As in the case of trioxane copolymers (see Sect. 3.2.3.2) the homopolymers of formaldehyde find application as engineering plastics. 

One should remember in this connection that many cases of spontaneous fission of excited (isomer) nuclear states with lifetimes about 10 2 sec (quite close to the time of addition of a new link to the growing polyformaldehyde chain near absolute zero of temperature) were observed and successfully studied after the pioneering works of Dubna scientists. 

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