Methyl rubber, poly

Methyl rubber Poly(2,3-dimethylbutadiene) Bayer, Germany (World War I)... [Pg.1138]

Poly(styrene) 1839 1930 Thermoplastics, foams Methyl rubbers 1912 1915 Elastomers... [Pg.9]

By combining elastomeric and brittle glassy phases it is often possible to obtain improved properties over a range of temperature and frequency. However, relatively little attention has been given to fatigue in IPNs, and to energy absorption in polyurethane rubber/poly(methyl methacrylate) (PU/PMMA) systems. [Pg.169]

MC MDI MEKP MF MMA MPEG MPF NBR NDI NR OPET OPP OSA PA PAEK PAI PAN PB PBAN PBI PBN PBS PBT PC PCD PCT PCTFE PE PEC PEG PEI PEK PEN PES PET PF PFA PI PIBI PMDI PMMA PMP PO PP PPA PPC PPO PPS PPSU Methyl cellulose Methylene diphenylene diisocyanate Methyl ethyl ketone peroxide Melamine formaldehyde Methyl methacrylate Polyethylene glycol monomethyl ether Melamine-phenol-formaldehyde Nitrile butyl rubber Naphthalene diisocyanate Natural rubber Oriented polyethylene terephthalate Oriented polypropylene Olefin-modified styrene-acrylonitrile Polyamide Poly(aryl ether-ketone) Poly(amide-imide) Polyacrylonitrile Polybutylene Poly(butadiene-acrylonitrile) Polybenzimidazole Polybutylene naphthalate Poly(butadiene-styrene) Poly(butylene terephthalate) Polycarbonate Polycarbodiimide Poly(cyclohexylene-dimethylene terephthalate) Polychlorotrifluoroethylene Polyethylene Chlorinated polyethylene Poly(ethylene glycol) Poly(ether-imide) Poly(ether-ketone) Polyethylene naphthalate Polyether sulfone Polyethylene terephthalate Phenol-formaldehyde copolymer Perfluoroalkoxy resin Polyimide Poly(isobutylene), Butyl rubber Polymeric methylene diphenylene diisocyanate Poly(methyl methacrylate) Poly(methylpentene) Polyolefins Polypropylene Polyphthalamide Chlorinated polypropylene Poly(phenylene oxide) Poly(phenylene sulfide) Poly(phenylene sulfone)... [Pg.959]

Abbreviations y x AFM AIBN BuMA Ca DCP DMA DMS DSC EGDMA EMA EPDM FT-IR HDPE HTV IPN LDPE LLDPE MA MAA MDI MMA PA PAC PB PBT PBuMA PDMS PDMS-NH2 interfacial tension viscosity ratio atomic force microscopy 2,2 -azobis(isobutyronitrile) butyl methacrylate capillary number dicumyl peroxide dynamic mechanical analysis dynamic mechanical spectroscopy differential scanning calorimetry ethylene glycol dimethacrylate ethyl methacrylate ethylene-propylene-diene rubber Fourier transform-infra-red high density polyethylene high temperature vulcanization interpenetrating polymer network low density polyethylene linear low density polyethylene maleic anhydride methacrylic acid 4,4 -diphenylmethanediisocyanate methyl methacrylate poly( amide) poly( acrylate) poly(butadiene) poly(butylene terephtalate) poly(butyl methacrylate) poly(dimethylsiloxane) amino-terminated poly(dimethylsiloxane)... [Pg.112]

On the other hand, some mechanically compatible blends as well as some dispersed two-phase systems have made respectable inroads into the commercial scene. Many of these are blends of low-impact resins with high-impact elastomeric polymers examples are polystyrene/rubber, poly (styrene-co-acrylonitrile) /rubber, poly (methyl methacrylate) /rubber, poly (ethylene propylene)/propylene rubber, and bis-A polycarbonate/ ABS as well as blends of polyvinyl chloride with ABS or PMMA or chlorinated polyethylene. [Pg.550]

FIG. 17.2 Generalized curve for the thermal conductivity of amorphous polymers. ( ) silicon rubberr (A) polyisobutylene (O) natural rubber (0) polypropylene (A) poly(trifluoro chloro ethylene) ( ) poly (ethylene terephthalate) (V) poly(vinyl chloride) ( ) poly(methyl methacrylate) ( ) poly(bisphenol carbonate) ( ) poly(vinyl carbazole) lines are drawn according to Eq. (17.9). [Pg.648]

FIG. 18.3 Activation energy of diffusion as a function of Tg for 21 different polymers from low to high temperatures, ( ) odd numbers (O) even numbers 1. Silicone rubber 2. Butadiene rubber 3. Hydropol (hydrogenated polybutadiene = amorphous polyethylene) 4. Styrene/butadiene rubber 5. Natural rubber 6. Butadiene/acrylonitrile rubber (80/20) 7. Butyl rubber 8. Ethylene/propylene rubber 9. Chloro-prene rubber (neoprene) 10. Poly(oxy methylene) 11. Butadiene/acrylonitrile rubber (60/40) 12. Polypropylene 13. Methyl rubber 14. Poly(viny[ acetate) 15. Nylon-11 16. Poly(ethyl methacrylate) 17. Polyethylene terephthalate) 18. Poly(vinyl chloride) 19. Polystyrene 20. Poly (bisphenol A carbonate) 21. Poly(2,6 dimethyl-p.phenylene oxide). [Pg.669]

PB PBI PBMA PBO PBT(H) PBTP PC PCHMA PCTFE PDAP PDMS PE PEHD PELD PEMD PEC PEEK PEG PEI PEK PEN PEO PES PET PF PI PIB PMA PMMA PMI PMP POB POM PP PPE PPP PPPE PPQ PPS PPSU PS PSU PTFE PTMT PU PUR Poly(n.butylene) Poly(benzimidazole) Poly(n.butyl methacrylate) Poly(benzoxazole) Poly(benzthiazole) Poly(butylene glycol terephthalate) Polycarbonate Poly(cyclohexyl methacrylate) Poly(chloro-trifluoro ethylene) Poly(diallyl phthalate) Poly(dimethyl siloxane) Polyethylene High density polyethylene Low density polyethylene Medium density polyethylene Chlorinated polyethylene Poly-ether-ether ketone poly(ethylene glycol) Poly-ether-imide Poly-ether ketone Poly(ethylene-2,6-naphthalene dicarboxylate) Poly(ethylene oxide) Poly-ether sulfone Poly(ethylene terephthalate) Phenol formaldehyde resin Polyimide Polyisobutylene Poly(methyl acrylate) Poly(methyl methacrylate) Poly(methacryl imide) Poly(methylpentene) Poly(hydroxy-benzoate) Polyoxymethylene = polyacetal = polyformaldehyde Polypropylene Poly (2,6-dimethyl-l,4-phenylene ether) = Poly(phenylene oxide) Polyp araphenylene Poly(2,6-diphenyl-l,4-phenylene ether) Poly(phenyl quinoxaline) Polyphenylene sulfide, polysulfide Polyphenylene sulfone Polystyrene Polysulfone Poly(tetrafluoroethylene) Poly(tetramethylene terephthalate) Polyurethane Polyurethane rubber... [Pg.939]

Bristow, G. M., "Phase Separation in Rubber-Poly(methyl methacrylate)-Solvent Systems," J. Appl. Polym. Sci., 2, 120 (1959). [Pg.168]

The utility of the DSC for studying polymer-polymer miscibility has been demonstrated for poly(vinyl chloride)/nitrile rubber polyfvinyl methyl ether)/poly-styrene and poly(2,6-dimethyl 1,4-diphenylene oxide)/poly(styrene-co-chloro-styrene)It has also been particularly useful for measuring the melting point depressions of crystalline polymers in blends Mn order to calculate the interaction parameter as will be discussed later. [Pg.142]

The first polymerization of isoprene in sealed bottles was reported in 1884 by Tilden. Methyl rubber was thermally polymerized at 70°C — the reaction required 3 to 6 months, giving poor quality products. In 1926 BASF developed sodium-initiated polymerization of butadiene known as Buna (for BUtadiene -I- Natrium). The first successful, general purpose rubbers were copolymers of butadiene with either styrene, Buna-S, or acrylonitrile, Buna-N [Tschunkur and Bock, 1933 Komad and Tschunkur, 1934]. Poly(2-chlorobutadiene), chloroprene [Carothers et ah, 1931], was introduced in 1931 by DuPont. Elastomeric polysulfides [Patrick, 1932] were... [Pg.2]

As natural rubber is a product of nature, its properties are determined by the biochemical pathway by which the polymer is synthesized in the plant. In the case of natural rubber the polymerization process cannot be tailored like that of synthetic rubbers. The only option to modify natural rubber is after it has been harvested from the tree. The important modified forms of natural rubber include hydrogenated natural rubber, chlorinated natural rubber, hydro-halogenated natural rubber, cyclized natural rubber, depolymerised liquid natural rubber, resin modified natural rubber, poly(methyl methacrylate) grafted natural rubber, poly(styrene) grafted natural rubber, and epoxidized natural rubber [33,34]. Thermoplastic natural rubber prepared by blending natural rubber and PP is considered as a physically modified form of natural rubber. [Pg.424]

The best-known elastomer is natural rubber, poly-isoprene (Scheme 6.10). Isoprene (Scheme 6.10a) is a liquid at room temperature, which polymerises readily to give the elastomer polyisoprene (Scheme 6.10b). The polymerisation produces two main geometrical isomers (see Section S2.1.) Natural rubber is the aU-c form of polyisoprene (Scheme 6.10c), in which the methyl (—CH3) groups and hydrogen (H) atoms are on the same side of the carbon-carbon double bond. Rubber latex, a milky liquid, is a suspension of rubber in water. It is found in many plants (e.g. in dandelions) as well as mbber... [Pg.184]

Contact lenses are the most common polymer product in ophthalmology. The basic requirements for this type of materials are (T)excellent optical properties with a refractive index similar to cornea good wettability and oxygen permeability ( ) biologically inert, degradation resistant and not chemically reactive to the transfer area ( ) with certain mechanical strength for intensive processing and stain and precipitation prevention. The common used contact lens material includes poly-P-hydroxy ethyl methacrylate, poly-P-hydroxy ethyl methacrylate-N-vinyl pyrrolidone, poly-P-hydroxy ethyl methacrylate, Poly-P-hydroxy ethyl methacrylate - methyl amyl acrylate and polymethyl methacrylate ester-N-vinyl pyrrolidone, etc. The artificial cornea can be prepared by silicon rubber, poly methyl... [Pg.177]

Meier [23] has derived equations relating block copolymer morphology to thermodynamics using lattice models. His model explains quantitatively the observations of Merrett [24] on the influence of preferential solvents on the mechanical properties of graft copolymers. Merrett found that, depending on the solvent used in casting films of a natural rubber/poly(methyl methacrylate) graft copolymer, he could obtain either a hard stiff film characteristic of poly(methyl methacrylate) or a soft, flexible film typical of natural rubber. He interpreted these results as follows a solvent for poly(methyl methacrylate) collapsed the... [Pg.146]

Oommen, Z., and Thomas, S.no access 1997. Compatibility studies of natural rubber/poly(methyl methacrylate) blends by viscometry and phase separation techniques. Journal of Materials Science 32(22) 6085-6094. [Pg.172]

During World War I, poly (dimethyl butadiene) was manufactured under the name methyl rubber as a substitute for the natural rubber that the Central Axis Powers lacked. H-type poly(dimethyl butadiene) was obtained by letting the monomer stand for three months in ventilated metal drums. The white, solid crystalline material thus obtained by popcorn polymerization becomes... [Pg.415]

As can be seen with benzene solutions of natural rubber-poly(methyl methacrylate) mixtures, the phase formation from solutions is regulated by the solubility ratios. Methanol is a stronger precipitant for natural rubber than for PMMA natural rubber forms the dispersed phase. In contrast, petroleum ether is a stronger precipitant for PMMA, and this forms the dispersed phase when petroleum ether is added. [Pg.669]

Standardized Malaysian rubber Poly(styrene-co-of-methyl styrene) (DIN ISO NS) Suspension-polymerized PVC... [Pg.809]

During World War I, poly(dimethyl butadiene) (methyl rubber) was manufactured as a substitute for the natural rubber that the Central Powers lacked when the war ended, its production was curtailed because of its relatively poor properties and high cost. 2,3-Dimethyl butadiene is produced from acetone via pinnacol ... [Pg.893]

Figure 1.13 Cis-trans isomerism of polyisoprene. The systematic name of isoprene is 1,3-butadiene, 2-methyl. Polyfisoprene 1,4-c s) is the main constituent of natural rubber. Poly Osoprene 1,4-trons) is the main constituent of gutta percha. Vinylic units (1-2) and (3-4) are present in synthetic rubbers.

Melt-processable rubber poly(a-methyl styrene)... [Pg.2162]

Methyl rubber n, Poly(2,3-dimethylbuta-diene). Manufactured by Bayer, Germany. a-Methylstyrene n. C6H5C(CH3)=CH2. A colorless liquid, easily polymerizable by heat or with catalysts, and typically... [Pg.616]

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