Developments in Ionic Polymers—2 - download pdf or read online

By R. A. M. Thomson (auth.), Alan D. Wilson, Havard J. Prosser (eds.)

ISBN-10: 9400941870

ISBN-13: 9789400941878

ISBN-10: 9401083606

ISBN-13: 9789401083607

Ionic polymers, like elephants, are more straightforward to understand than to outline. numerous equipment of type were tried yet none is utterly passable as a result severe variety of ionic polymers, which variety from the natural, water-soluble polyelectrolytes, via hydrogels and ionomer carboxylate rubbers, to the just about infusible inorganic silicate minerals. accordingly, a basic type isn't just tough, yet has minimum application. in spite of the fact that, there are a few features of those fabrics that are meant to be highlighted. The position of counterions is the numerous one. those ions, both singly or as clusters, participate in the formation of ionic bonds that have a various structural function. usually they act as crosslinks, yet within the halato-polymers the ionic bonds shape an essential component of the polymer spine itself. Conversely, in polymers include­ ing covalent crosslinks, corresponding to the ion-exchange resins, the coun­ terions have almost no structural function to play, considering the fact that they stay in cage-like buildings with out affecting the crosslinking, and are comfortably exchanged. they're, might be, top defined as ion-containing polymers instead of structural ionic polymers. one other the most important issue is the function of water in ionic polymers. The presence of ionic bonds implies that there's a tendency for those fabrics to engage with water. the place the ionic polymer includes a excessive percentage of ionic devices, it acts as a hydrogel and will be hugely soluble. Such interactions with water lessen sharply because the ionic content material is decreased, notwithstanding even then water can act as a plasticiser.

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If this is strong, the probable mechanism of the attack is: CH~ ~ lN,+J R X- X-CHz-CH 6~ ,+ X- R R= H or alkyl whereas, if it is weak, attack by unreacted monomer provides a more likely route and the product will be the ionene as indicated. Hoover and Butler6 and Luskin 187 have discussed the possible reaction in 54 R. A. M. THOMSON ~ CHz==CH~N + CHz==CH -0+ \ ,1N-R X- CHz==CH-Q4CH2-CH==()-1-R XR=H or alkyl considerable detail in their reviews. Salamone,284 in a more recent paper, has confirmed the existence of a free-radical process in the spontaneous polymerization.

Thereafter, benzoin decomposition by UV irradiation completes the conversion in a 5 min period. Another example239 ,24o is the combination of similar redox systems with an azo initiator. Under the conditions used, 80% conversion was attained in 4 h at 5-40°C. Thereafter, heating for 1 h at 70-90°C caused expansion of the polymer molecules and enabled almost complete conversion to a soluble, non-gelling polymer. The polymerization process is, in common with the polymerization of other ionic monomers, sensitive to the reaction medium.

Complex quaternary compounds are also readily formed. A typical example 225 is the formation of salts with the structure XLV (R3 = H, Me; Rl, R 2 =C I _ 3 hydroxyethylene, alkyl; Z=CH2, hydroxypropylene; X = CI, Br, CI04, N0 3, p-Me·C6 H 4·S0 3 or AcO). Typically these salts are formed by reaction with reactants such as 46 R. A. M. THOMSON N,N-diethylethanolamine, neutralized with gaseous HCI in propane2-01ltoluene, and treated for 5 h at 60°C with glycidyl methacrylate (XLVI). /CH3 CHz=C"", C-O--CH2-CH-CH2 V ~ XLVI Acrylamide derivatives are also easily converted to the quaternary ammonium form.

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Developments in Ionic Polymers—2 by R. A. M. Thomson (auth.), Alan D. Wilson, Havard J. Prosser (eds.)

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