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Styrene-co-N-

Figure 2 Property distributions in a linear copolymer composition distribution, molecular weight distribution and sequence length distribution of poly styrene-co-n-butyl methacrylate). (Styrene units are represented by "A and n-butyl methacrylate units by B".)... Figure 2 Property distributions in a linear copolymer composition distribution, molecular weight distribution and sequence length distribution of poly styrene-co-n-butyl methacrylate). (Styrene units are represented by "A and n-butyl methacrylate units by B".)...
Figure 8 (1., 6) shows the fractionation obtained by analyzing a mixture of polystyrene, poly(styrene co-n-butyl methacrylate) and poly(n-butyl methacrylate) with various n-heptane concentrations. [Pg.68]

Figure 8 Two series of Orthogonal Chromatography runs showing the effec of % n-hept me in the mobile phase of SEC 2 on the fractionation (AA polystyrene, AB poly(styrene co-n-butyl methacrylate) BB poly n-butyl methacrylate). (Reproduced fran Ref. 6. Copyright 1983, American Chemical Society.)... Figure 8 Two series of Orthogonal Chromatography runs showing the effec of % n-hept me in the mobile phase of SEC 2 on the fractionation (AA polystyrene, AB poly(styrene co-n-butyl methacrylate) BB poly n-butyl methacrylate). (Reproduced fran Ref. 6. Copyright 1983, American Chemical Society.)...
The clearest instances of contact charging by ion transfer are exhibited by ionomers, e.g. poly(styrene-co-N-methyl-4-vinyl-pyridinium toluenesulphonate),... [Pg.243]

Fig. 7.19 Graph of charge-to-mass ratio versus ionic content for particles of a blend of styrene-co-N-methyl-4-vinyl-pyridinium toluenesulphonate iono-mer with a styrene-co-butyl methacrylate copolymer, charged by rolling with coated beads. Reprinted with permission from Diaz et al. (1992). Copyright of the American Chemical Society. Fig. 7.19 Graph of charge-to-mass ratio versus ionic content for particles of a blend of styrene-co-N-methyl-4-vinyl-pyridinium toluenesulphonate iono-mer with a styrene-co-butyl methacrylate copolymer, charged by rolling with coated beads. Reprinted with permission from Diaz et al. (1992). Copyright of the American Chemical Society.
Figure 1. C-NMR spectrum of poly (styrene-co-N-(p-t-butyloxy carbonyloxyphenyl) maleimide ... Figure 1. C-NMR spectrum of poly (styrene-co-N-(p-t-butyloxy carbonyloxyphenyl) maleimide ...
Poly(styrene-co-N-vinylbenzyI-N -inethyl-4,4 -bipyridine) di-chloiide (2). N-Methyl-4,4 -bipyridine was attached to chloromethylated polystyrene via a quatemization reaction. Chloromethylated polystyrene (1.00 g) and 1.26 g of N-methyl-4,4 -bipyridine were dissolved in 100 mL of CHCI3 and 100 mL of CH3CN. The pale yellow solution was refluxed for 72 h, after which much of the solvent was removed. An ion-exchange column was prepared... [Pg.363]

The t-BOC protection group chemistry has been extended to other aqueous-base soluble polymers such as poly[styrene-co-N-(4-hydroxyphenyl)maleimide], ° poly(styrene-co-maleimide), poly(4-hydroxystyrene sulfone), and poly(4-hydroxy-a-methylstyrene) used in lithographic applications. Even novolac resins have been successfully protected with the t-BOC group,which has resulted in significant reduction of the DUV absorption of these resins. ... [Pg.352]

Moraes RP, Valera TS, Demarquette NR, et al. (2009) Influence of granulometry and organic treatment of a BrazUian montmorillonite on the properties of poly(styrene-co-n-butyl acrylate)/layered silicate nanocomposites prepared by miniemulsion polymerization. J Appl... [Pg.45]

X. Ding, Z. Sun, W. Zhang, Y. Peng, A.S.C. Chan, P. Li, Characterization of Fe304/poly (styrene-co-N-isopropylacrylamide) magnetic particles with temperarnre sensitivity. Colloid Polym. Sci. 278, 459-463 (2000)... [Pg.264]

Schmidt-Naake, G. and Butz, S. 1996. Living free radical donor-acceptor copolymerization of styrene and N-cyclohexyl maleimide and the synthesis of poly[styrene-co-(N-chlohexylmaleimide)]/polystyrene block copolymers. Macrgmoleadat a i ... [Pg.113]

Lokaj, J., Vlcek, R, and Kriz, J. 1999. Poly(styrene-co-N-butylmaleimide) macroinitiators by controlled autopolymerization and related block copolymers. Journal of Applied Polymer Science 74 2378-2385. [Pg.113]

The chemical modification of homopolymers such as polyvinylchloride, polyethylene, poly(chloroalkylene sulfides), polysulfones,poly-chloromethylstyrene, polyisobutylene, polysodium acrylate, polyvinyl alcohol, polyvinyl chloroformate, sulfonated polystyrene block and graft copolymers such as poly(styrene-block-ethylene-co-butylene-block-styrene), poly(1,4-polybutadiene-block ethylene oxide), star chlorine-telechelic polyisobutylene, poly(lsobutylene-co-2,3-dimethy1-1,3-butadiene), poly(styrene-co-N-butylmethacrylate) cellulose, dex-tran and inulin, is described. [Pg.425]

Stoiljkovic A, Venkatesh R, Klimov E, Raman V, Wendorff JH, Greiner A (2009) Poly(styrene-co-n-butyl acrylate) nanofibers with excellent stability against water by electrospinning from aqueous colloidal dispersions. Macromolecules 42 6147-6151... [Pg.426]

DJA Djadoun, S., Karasz, F.E., and Hamou, A.S.H., Blends of poly(isobutyl methacrylate) with poly(styrene-co-acrylic acid) and of poly(isohutyl methacrylate-co-acrylic acid) with poly(styrene-co-N,N-dimethyl-aminoethyl methacrylate), Thermochim. Acta, 282/283, 399, 1996. [Pg.152]

Poly(styrene-co-n-butyl methacrylate) Liquid absorption, silica gel, ... [Pg.1852]

See other pages where Styrene-co-N- is mentioned: [Pg.65]    [Pg.207]    [Pg.244]    [Pg.204]    [Pg.71]    [Pg.249]    [Pg.249]    [Pg.360]    [Pg.59]    [Pg.359]    [Pg.48]    [Pg.300]    [Pg.72]    [Pg.207]    [Pg.211]    [Pg.224]    [Pg.1852]    [Pg.54]   
See also in sourсe #XX -- [ Pg.249 ]



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