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CYCLOHEXANE, 1 ,2-DIMETHYLENE

Cyclohexanamine, N-[(2-bromo-4,5-dimethoxyphenyl)methylene]-, 65, 108 Cyclohexanamine, N-[(2-iodo-4,5-dimethoxyphenyl)methylene]-, 65, 108 CYCLOHEXANE, 1,2-BIS(METHYLENE)-, 65, 90 Cyclohexane, 1,1-diethoxy-, 65, 17 CYCLOHEXANE, 1,2-DIMETHYLENE, 65, 90... [Pg.274]

OLEFIN POLYMERS - POLYMERS OF HIGHER OLEFINS] (Vol 17) Poly(l,4-cyclohexane-dimethylene terephthalate) [24936-69-4]... [Pg.779]

Chain-Extension of a,co-Dihydroxy-Terminated Oligo(l,3-Propylene-Co-1,4-Cyclohexane-dimethylene Succinate)... [Pg.157]

Poly(ethylene-co-1,4-cyclohexane dimethylene terephthalate) The thermal and photochemical oxidation processes of a polyester based on poly(ethylene-co-l,4-cyclohexanedimethylene terephthalate) (PECT) with approximately 30% of 1,4-cyclohexanedimethanol have been studied by means of chemiluminescence [88], Also, the stabilization activity of some commercial antioxidants has been evaluated, and it has been related to hydroperoxide levels in the polymer. [Pg.119]

Poly(l,4.butylene adipate) Polybutyleneterephthalate Bisphenol-A polycarbonate Poly( 1,4-cyclohexane-dimethylene succinate)... [Pg.285]

Ester Single Eg I hadA/w = 1.4—2.1 kg/mol and had 1.3-7.7 wt% OH groups II was butylene adipate, butylene sebacate, caprolactone, 1,4-cyclohexane dimethylene succinate, decamethylene sebacate, and 2,2-dimethyl-l, 3-propylene adipate of hexamethylene sebacate high OH content of I favored miscibility Barnum et al. (1981), Woo et al. (1984a)... [Pg.1939]

Cyclohexane-dimethylene terephthalate Single Tg melt transpareait Semicrystalline Cruz et al. (1979c), Landry and Hendrichs (1989), Mohn et al. (1979)... [Pg.1958]

Carbonate of bisphenol-A Cyclohexane dimethylene succinate Single Tg - Shah et al. (1986)... [Pg.2065]

VCI2-VC PCL other polyesters VCL2-VC (13.5 wt% VC) miscible with PCL, poly(2.2-dimethyl-1,3-propylene adipate) poly( 1,4-cyclohexane dimethylene succinate) and poly(2,2-dimethyl- 1,3-propylene succinate) 866... [Pg.186]

Other statistical copolymers that have been found to exhibit isodimorphic behavior include poly()3-hydroxybutyrate-co-)3-hydroxyvalerate) [87, 88], poly (butylene terephthalate-co-butylene-2,6-naphthalate) [89], poly(butylene terephthalate-co-l,4-cyclohexane dimethylene terephthalate) [90], and poly(butylene terephthalate-co-cyclopentane dimethylene terephthalate) [90]. In all cases, measurable crystallinity was observed over the entire copolymer composition range. An abrupt transition in the crystal structure was detected at some intermediate composition and was correlated with a eutectic-Uke minimum in the melting temperature [87-90]. [Pg.337]

Poly(oxyethyleneoxyterephthalate)/poly( 1,4-cyclohexane dimethylene terephthalate) (random copolymers) 100/0, mol%... [Pg.1205]

Cyclohexane-dimethylene Single Tg, melt transparent Semicrystalline 174,486,581... [Pg.1293]

Carbonate of bisphenol-A Ethyl methacrylate Cyclohexane dimethylene succinate Maleic anhydride-eo-styrene Single Tg Single Tg 16/16 I had 25% acrylonitrile 738 74... [Pg.1322]

Poly( 1,4-cyclohexane dimethylene terephthalate-eo-ethylene terephthalate) Dimethyl terephthalate-ethylene glycol-1,4-bis(hydroxy niethyl)-cyclohexane copolymer 25640-14-6 1,4-Benzenedicarlx)xylic acid, dimethyl ester, polymer with 1,4-cyclohexanedimethanol and 2-ethanediol R (C i()H 10O4 CsH 16O2 C2H602)... [Pg.2284]

Note, as discussed in Reference 8, 1,3-dimethylenecyclohexane is some 10 kJ mol 1 more stable than its 1,4-isomer. The 1,3- and 1,4-dimethylene compounds are stabilized relative to the monomethylene compound by 19 and 9 kJmol-1, respectively, while the corresponding diketones are stabilized relative to the monoketone by some 7 and 4 kJmol-1. These results are consonant with the 1,3-bis-sp2 cyclohexanes being more stabilized than their 1,4-counterpart, but electrostatic destabilization affecting the /J-di ketone and not particularly the bismethylene compound. [Pg.608]

Ball and Hardwood (105a) reported an unusual cationic intra-intermolecular polymerization in the case of 1,4-dimethylene cyclohexane. The best catalyst was BF- gas in methvlene chloride solution at -78 to -40° C. [Pg.520]


See other pages where CYCLOHEXANE, 1 ,2-DIMETHYLENE is mentioned: [Pg.239]    [Pg.243]    [Pg.204]    [Pg.779]    [Pg.928]    [Pg.930]    [Pg.269]    [Pg.269]    [Pg.272]    [Pg.272]    [Pg.272]    [Pg.340]    [Pg.362]    [Pg.1288]    [Pg.1293]    [Pg.373]    [Pg.107]    [Pg.12]    [Pg.275]    [Pg.327]    [Pg.239]    [Pg.243]    [Pg.376]    [Pg.930]    [Pg.204]   
See also in sourсe #XX -- [ Pg.65 , Pg.90 ]




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1,2-DIMETHYLENECYCLOHEXANE: CYCLOHEXANE, 1,2-DIMETHYLENE

Poly(l,4- cyclohexane dimethylene

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