Polystyrene-poly methyl

Figure Bl.19.30. Height and friction images of a spin-cast polystyrene-poly(methyl methacrylate) blend obtained with (a) gold and (b) silica probes under perfluorodecalin. Note the reversal of frictional contrast and the high spatial resolution. (Taken from [142], figure 7.)...

Figure 9.17 Plot of log [i ]M versus retention volume for various polymers, showing how different systems are represented by a single calibration curve when data are represented in this manner. The polymers used include linear and branched polystyrene, poly(methyl methacrylate), poly(vinyl chloride), poly(phenyl siloxane), polybutadiene, and branched, block, and graft copolymers of styrene and methyl methacrylate. [From Z. Grubisec, P. Rempp, and H. Benoit, Polym. Lett. 5 753 (1967), used with permission of Wiley.]...

In principle, A can be any polymer normally regarded as a hard thermoplastic, eg, polystyrene, poly(methyl methacrylate), or polypropylene, and B can be any polymer normally regarded as elastomeric, eg, polyisoprene, polybutadiene, polyisobutylene, or polydimethylsiloxane (Table 2). 

Amorphous thermoplastics These are made from polymers which have a sufficiently irregular molecular structure to prevent them from crystallising in any way. Examples of such materials are polystyrene, poly methyl methacrylate and polyvinyl chloride. 

Gong, Y., Huang, H., Hu, Z., Chen, Y, Chen, D Wang, Z. and He, X. (2006) Inverted to normal phase transition in solution-cast polystyrene-poly(methyl methacrylate) block copolymer thin films. Macromolecules, 39, 3369-3376. 

Much work on the preparation of nonaqueous polymer dispersions has involved the radical polymerization of acrylic monomers in the presence of copolymers having the A block the same as the acrylic polymer in the particle core 2). The preparation of polymer dispersions other than polystyrene in the presence of a PS-PDMS diblock copolymer is of interest because effective anchoring of the copolymer may be influenced by the degree of compatibility between the PS anchor block and the polymer molecules in the particle core. The present paper describes the interpretation of experimental studies performed with the aim of determining the mode of anchoring of PS blocks to polystyrene, poly(methyl methacrylate), and poly(vinyl acetate) (PVA) particles. 

Emulsion polymerization is used for 10-15% of global polymer production, including such industrially important polymers as poly(acrylonitrile-butadiene-styrene) (ABS), polystyrene, poly(methyl methacrylate), and poly (vinyl acetate) [196]. These are made from aqueous solutions with high concentrations of suspended solids. The important components have unsaturated carbon-carbon double bonds. Raman spectroscopy is well-suited to address these challenges, though the heterogeneity of the mixture sometimes presents challenges. New sample interfaces, such as WAI and transmission mode, that have shown promise in pharmaceutical suspensions are anticipated to help here also. 

Monomer and initiator must be soluble in the liquid and the solvent must have the desired chain-transfer characteristics, boiling point (above the temperature necessary to carry out the polymerization and low enough to allow for ready removal if the polymer is recovered by solvent evaporation). The presence of the solvent assists in heat removal and control (as it also does for suspension and emulsion polymerization systems). Polymer yield per reaction volume is lower than for bulk reactions. Also, solvent recovery and removal (from the polymer) is necessary. Many free radical and ionic polymerizations are carried out utilizing solution polymerization including water-soluble polymers prepared in aqueous solution (namely poly(acrylic acid), polyacrylamide, and poly(A-vinylpyrrolidinone). Polystyrene, poly(methyl methacrylate), poly(vinyl chloride), and polybutadiene are prepared from organic solution polymerizations. 

Deters (14) vibromilled a blend of cellulose and cellulose triacetate. The acetic acid content of cellulose acetate decreased with grinding time (40 h) while that of the cellulose increased, suggesting the formation of a block or graft copolymer or of an esterification reaction by acetic acid developed by mechanical reaction. Baramboim (/5) dissolved separately in CO polystyrene, poly(methyl methacrylate), and poly(vinyl acetate). After mixing equal volumes of solutions of equivalent polymer concentration, the solvent was evaporated at 50° C under vacuum and the resultant product ball-milled. The examination of the ball-milled products showed the formation of free radicals which copolymerized. 

Examples of known phosphazene polymer blends are those in which phosphazenes with methylamino, trifluoroethoxy, phenoxy, or oligo-ethyleneoxy side groups form blends with poly(vinyl chloride), polystyrene, poly(methyl methacrylate), or polyethylene oxide).97 100 IPNs have been produced from [NP(OCH2CH2OCH2CH2OCH3)2] (MEEP) and poly(methyl methacrylate).101-103 In addition, a special type of IPN has been reported in which a water-soluble polyphosphazene such as MEEP forms an IPN with a silicate or titanate network generated by hydrolysis of tetraethoxysilane or tetraalkoxytitanane.104 These materials are polyphosphazene/ceramic composites, which have been described as suitable materials for the preparation of antistatic layers in the manufacture of photographic film. 

Han XM, Shen J, Huang HX, Tomasko DL, Lee LJ (2007) C02 foaming based on polystyrene/poly(methyl methacrylate) blend and nanoclay. Polym Eng Sci 47 103-111... 

Fracture Surface Morphology and Phase Relationships of Polystyrene/Poly(methyl Methacrylate) Systems... 

Not surprisingly, as the science of macromolecules emerged, a large number of synthetic polymers went into commercial production for the first time. These include polystyrene, poly(methyl methacrylate), nylon 6.6, polyethylene, poly(vinyl chloride), styrene-butadiene rubber, silicones and polytetrafluoroethylene, as well as many other. From the 1950s onwards regular advances, too numerous to mention here, have continued to stimulate both scientific and industrial progress. 

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