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Polyketones, Polyureas

A process for the preparation of aryl polyether-polyketones by electrophilic polymerization has been disclosed [260]. The polymers, having excellent high-temperature resistance, are prepared by the reaction of carboxylic acid halides in [Pg.581]


An important direct use of phosgene is in the preparation of polymers. Polycarbonate is the most significant and commercially valuable material (see Polycarbonates). However, the use of phosgene has been described for other polymer systems, eg, fiber-forming polymeric polyketones and polyureas (90,91). [Pg.315]

Aliphatic iodine derivatives, 14 376 Aliphatic ketones, 14 563, 571, 581-585 reactions of, 16 331-332 Aliphatic monothiopolyesters, 23 739 Aliphatic nitration, 12 187 Aliphatic peroxyacids, 13 464 Aliphatic peroxycarboxylic acids, 18 463 Aliphatic phosphines, 19 60 Aliphatic polyamides (PA), 10 207-210 19 713, 739. See also Aromatic polyamides PA entries producers of, 10 210 properties of, 10 208, 209t Aliphatic polycarbonates, 24 703 preparation of, 19 798 Aliphatic polyketones (PK), 10 197 costs of, 10 222 properties of, 10 198t Aliphatic poly(monosulfide)s, 23 702-704 Aliphatic polyphosphonate dyes, 9 480 Aliphatic poly(polysulfide)s, 23 711 Aliphatic polysulfides, 23 734 Aliphatic polysulfoxides, 23 733 miscibility of, 23 735 Aliphatic polyurea preparation, carbonyl sulfide in, 23 625... [Pg.28]


See other pages where Polyketones, Polyureas is mentioned: [Pg.212]    [Pg.581]    [Pg.212]    [Pg.581]    [Pg.487]    [Pg.348]    [Pg.129]    [Pg.226]   


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Polyketonates

Polyketone

Polyurea

Polyureas

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