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Poly isocyanate treated

Potential Uses of These Polymers. We have studied the phenyl isocyanate modification of poly(vinyl alcohol) as a model system. Many uses exist for carbamates as medicines, pesticides and herbicides (67,68). For example, ethyl carbamate has been used to treat leukemia and multiple myeloma. Ethyl carbamate has also been used as an antidote for central nervous system poisoning by strychnine. The tranquilizer Meprobamate is a carbamate derivitive. Numerous pesticides and herbicides, such as Sevin and Propham, are also carbamate derivatives. Propham is isopropyl N-phenylcarbamate which bears a strong resemblence to the polymers of Equation 21, and this compound is used as a preemergence herbicide. Numerous other close analogs could be cited also. We might note also that the N-phenyl carbamoyl unit bears... [Pg.98]

Biomer is a commercially available, medical grade segmented poly(ether urethane urea) (PEUU), which is prepared by treating an isocyanate-capped polyetherurethane with diamine (e.g. ethylenediamine) as chain extender... [Pg.3]

This limitation is overcome when the elastomer is cast from a mixture consisting of a linear polyester or poly ether, diisocyanate and glycol or diamine. In this process, the hydroxy-terminated polymer (e.g., poly(ethylene adipate) or poly(oxytetramethylene) glycol) is treated with an excess of diisocyanate (e.g., naphthylene 1,5-diisocyanate, tolylene diisocyanate or diphenylmethane 4,4 -diisocyanate). The product is a pre-polymer which is, in effect, a mixture of isocyanate-terminated polymer and unreacted diisocyanate. The pre-polymer is then mixed with either a glycol (e.g., 1,4-butanediol or 1,6-hexanediol) or diamine (which is usually a deactivated amine such as 3,3 -dichloro4,4 -diamino-diphenylmethane (MOCA)). The mixture is poured into a heated mould where it quickly sets. After about 30 mins the casting is removed from the mould and cured at about 110°C for 24 hours. [Pg.335]

Polyurethane fibres of a kind different to those described above have become important within the last decade these are elastomeric fibres, which are commonly called spandex fibres. These products are made either by solution spinning or by reaction spinning. In the first process, a hydroxy-terminated polyester (e.g., an adipate) or polyether (e.g., poly(oxytetramethylene) glycol) is treated with an excess of diisocyanate (e.g., tolylene diisocyanate) to give an isocyanate-terminated pre-polymer similar to those used for cast elastomers (Section 14.6.1). The pre-polymer is dissolved in a strongly polar solvent (e.g., dimethylformamide) and treated with an aliphatic diamine or hydrazine to effect chain extension with hydrazine the following reaction occurs ... [Pg.341]

In the majority of cases, the polymer was named according to its structure, particularly when the CRU was composed of two or more subunits following each other in a regular fashion. An example is poly(ethylene terephthalate). With more complicated structures, the CRU was divided into its possible subunits, each of which was treated as a bivalent radical and so named. One of the subunits was treated as the parent compound, for example, the terephthalic acid of the above example. For poly(amides) and poly(esters), the acid was chosen as the parent compound for poly(urethanes) it was the isocyanate. [Pg.875]


See other pages where Poly isocyanate treated is mentioned: [Pg.394]    [Pg.314]    [Pg.341]    [Pg.341]    [Pg.280]    [Pg.186]    [Pg.357]    [Pg.4145]    [Pg.6661]    [Pg.245]    [Pg.266]    [Pg.377]   
See also in sourсe #XX -- [ Pg.293 ]




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