1992
DOI: 10.1021/j100182a088
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Copolymerization of acrylamide and a hdydrophobic monomer in an aqueous micellar medium: effect of the surfactant on the copolymer microstructure

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Cited by 164 publications
(181 citation statements)
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“…The peaks at 48 ppm are attributed to the carbons of ACH 2 A. It can be testified that the copolymer of AM and St had been prepared by the 1 H-NMR, 13 C-NMR, and IR analyses.…”
Section: C-nmr Characterizationmentioning
confidence: 96%
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“…The peaks at 48 ppm are attributed to the carbons of ACH 2 A. It can be testified that the copolymer of AM and St had been prepared by the 1 H-NMR, 13 C-NMR, and IR analyses.…”
Section: C-nmr Characterizationmentioning
confidence: 96%
“…As far as to we know, the preparation of PAM-b-PSt by this method was not reported. Compared with micelle method 13 and general microemulsion method, 9 the method cannot only avoid the complicate purified back treatment of surfactant, but can also make the efficiency of block copolymerization higher.…”
Section: Introductionmentioning
confidence: 99%
“…The copolymers of AM, AMPS, and BAAM [poly(Narylalkylacrylamide-co-acrylamide-co-2-acrylamide-2-methylpropanesulfate) (PBAMS)] were prepared by micellar copolymerization 18,19 with sodium dodecyl sulfate (SDS) as the surfactant and ammonium persulfate/sodium bisulfite as the redox free-radical initiator. Each reaction was conducted in a 100-mL, threenecked, round flask equipped with a mechanical stirrer and nitrogen inlet and outlet.…”
Section: Materials and Sample Preparationmentioning
confidence: 99%
“…18,[23][24][25] Phenyl groups are well known to induce van der Waals interactions because of their planar and polarizable structure, and so the incorporation of an aromatic group into hydrophobic groups can stabilize the hydrophobic associations involved with alkyl chains. Furthermore, phenyl groups can act as spacers, increasing the rigidity of the structure.…”
Section: Introductionmentioning
confidence: 99%
“…Micelles can concentrate the reactants within their small volumes (1)(2)(3)(4); stabilize substrates, intermediates, or products (5,6); and orient substrates (7)(8)(9) so that ionization potential and oxidation-reduction properties, dissociation constants, physical properties, quantum efficiencies, and reactivity are changed (10)(11)(12). Thus micelles can also alter the reaction rate, mechanism (13), and regio-and stereochemistry (14,15).…”
Section: Introductionmentioning
confidence: 99%