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Chain sulfonates

Emulsion Polymerization. In this method, polymerization is initiated by a water-soluble catalyst, eg, a persulfate or a redox system, within the micelles formed by an emulsifying agent (11). The choice of the emulsifier is important because acrylates are readily hydrolyzed under basic conditions (11). As a consequence, the commonly used salts of fatty acids (soaps) are preferably substituted by salts of long-chain sulfonic acids, since they operate well under neutral and acid conditions (12). After polymerization is complete the excess monomer is steam-stripped, and the polymer is coagulated with a salt solution the cmmbs are washed, dried, and finally baled. [Pg.474]

TABLE 8. (Partly) open-chain sulfones from sulfenes and their dimers... [Pg.198]

These methods use sulfur dioxide as a building block, generally for cyclic sulfones. However, since several variations allow the preparation of open-chain sulfones too (Section III.D), several selected examples will be presented here. [Pg.206]

Polyether-PA segmented copolymers, synthesizing, 191-192 Polyether polyols, 200, 205, 211-212 synthesis of, 223, 224 Poly(ether sulfone) (PES), 327. See also Poly(arylene ether sulfone)s Poly(phenylene ether sulfone) chains Sulfonated poly (ary lene ether sulfone)... [Pg.596]


See other pages where Chain sulfonates is mentioned: [Pg.25]    [Pg.165]    [Pg.167]    [Pg.169]    [Pg.171]    [Pg.173]    [Pg.175]    [Pg.177]    [Pg.179]    [Pg.181]    [Pg.185]    [Pg.189]    [Pg.191]    [Pg.193]    [Pg.195]    [Pg.197]    [Pg.199]    [Pg.201]    [Pg.203]    [Pg.205]    [Pg.209]    [Pg.215]    [Pg.217]    [Pg.219]    [Pg.221]    [Pg.223]    [Pg.225]    [Pg.227]    [Pg.229]    [Pg.232]    [Pg.1213]    [Pg.1215]    [Pg.1217]    [Pg.1233]    [Pg.167]    [Pg.169]    [Pg.171]    [Pg.173]    [Pg.175]    [Pg.177]    [Pg.179]    [Pg.183]    [Pg.185]    [Pg.187]    [Pg.189]    [Pg.191]   
See also in sourсe #XX -- [ Pg.177 , Pg.427 ]




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