Polyoxymethylene

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Polyoxymethylene (POM), also known as polyacetal, acetal resin, polytrioxane, polyformaldehyde, and paraformaldehyde, is an engineering plastic used to make gears, bushings and other mechanical parts (cf. nylon, Teflon, UHMWPE). The most important polyacetal resin, it is a thermoplastic with good physical and processing properties. It is also sold under the trade names Delrin, Kepital, Celcon, "Hostaform" and Ultraform, the last three being copolymers. Its chemical formula is -(-O-CH2-)n-.

Since formaldehyde polymerizes in water, formalin-preserving solutions actually contain very little formaldehyde in the form of H2CO monomer; most of it forms short chains of polyformaldehyde. A few percent methanol is often added to limit the extent of polymerization.

Synthesis

To make polyoxymethylene homopolymer, anhydrous formaldehyde must be generated. The principal method is by reaction of the aqueous formaldehyde with an alcohol to create a hemiformal, dehydration of the hemiformal/water mixture (either by extraction or vacuum distillation) and release of the formaldehyde by heating the hemiformal. The formaldehyde is then polymerized by anionic catalysis and the resulting polymer stabilized by reaction with acetic anhydride.

To make polyoxymethylene copolymer, formaldehyde is generally converted to trioxane. This is done by acid catalysis (either sulfuric acid or acidic ion exchange resins) and concurrent removal of the trioxane by distillation or extraction. The trioxane is then dried to remove all water and other active hydrogen containing impurities.

The co-monomer is typically dioxolane but ethylene oxide can also be used. Dioxolane is formed by reaction of ethylene glycol with a formaldehyde source (trioxane or concentrated aqueous formaldehyde) over an acid catalyst. Other diols can also be used.

Trioxane and Dioxolane are polymerized using an acid catalyst, often boron trifluoride etherate, BF3·OEt2. The polymerization can take place in a non-polar solvent (in which case the polymer forms as a slurry) or in the melt (e.g. an extruder). After polymerization, the acidic catalyst must be deactivated and the polymer stabilized by heat.

Stable polymer is melt compounded, adding thermal and oxidative stabilizers and optionally lubricants and miscellaneous fillers.

Applications

2 to 4 % solutions of polyformaldehyde in phosphate buffered saline are used as a fixative. It is commonly used in in situ hybridization including the TUNEL staining. In the TUNEL assay polyformaldehyde fixation increase the accessibility of the intracellular component therefore increasing the sensitivity of the staining.

Polyoxymethylene is used in many applications including parts in vehicles from automobiles to spacecraft

External links

cs:Paraformaldehyd de:Paraformaldehydfr:Polyoxyméthylène it:Poliossimetileneuk:Поліформальдегід


Acknowledgement and Attribution Regarding Sources of Content

Some of the initial content on this page may be incorporated in part from copyleft sources in the public domain including wikis such as Wikipedia and AskDrWiki. Drug information for patients came from the The National Library of Medicine. Infectious disease information may have come from the Centers for Disease Control (CDC). Differential Diagnoses are drawn from clinicians as well as an amalgamation of 3 sources: 1.The Disease Database; 2. Kahan, Scott, Smith, Ellen G. In A Page: Signs and Symptoms. Malden, Massachusetts: Blackwell Publishing, 2004:3; 3. Sailer, Christian, Wasner, Susanne. Differential Diagnosis Pocket. Hermosa Beach, CA: Borm Bruckmeir Publishing LLC, 2002:7 .

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