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Ethylene carboxylated

W.L. Vaughn and T.J. McKeand, Jr, Ionomers of ethylene/carboxylic acid copolymers, US Patent 5320905, assigned to The Dow Chemical... [Pg.148]

Savignac, P, Snoussi, M., and Coutrot, P, Carboxychloro olefination. A convenient synthesis of a-chloro-a,P-ethylenic carboxylic acids, Synth. Commun., 8, 19, 1978. [Pg.146]

T he type of counterion used in an ion-containing polymer can have a substantial effect on the physical properties of the material. Many studies have been made in the past comparing the properties of metal- or ammonium-neutralized ionomers two recent books on ion-containing polymers present a comprehensive review of the literature (1,2). There is a wealth of information comparing different metal counterions in neutralized or partially neutralized ethylene-carboxylic acid copolymers. Rees and Vaughan studied the melt flow and tensile properties of... [Pg.55]

ETHYLENE CARBOXYLIC ACID (79-10-7) C3H4O2 Forms explosive mixture with air [explosion limits in air (vol %) 2.4 to 8.0 flashpoint 130°F/54°C cc autoignition tenqi 820 = F/438°C 680°F/360 = C Fire Rating 2]. The uninhibited acid (usually inhibited with hydroquinone) will be extrasensitive to light, heat, oxidizers including... [Pg.460]

ETHYLENE CARBOXYLIC ACID (79-10-7) Forms explosive mixture with air (flash point 124°F/51°C). Light, heat, or peroxides can cause explosive polymerization. Incompatible with strong acids, alkalis, ammonia, amines, isocyanates, alkylene oxides, epichlorohydrin, oxidizers, toluenediamine, pyridine, methyl pyridine, w-methyl pyrrolidone, 2-methyl-6-ethyl aniline, aniline, ethylene diamine, ethyleneimine, 2-aminoethanol. Severely corrodes carbon steel and iron attacks other metals. Flow or agitation of substance may generate electrostatic charges due to low conductivity. The uninhibited vapors may form polymers in plug vents, confined spaces, or flame arresters of storage tanks. [Pg.525]

Reduction of ethylenic carboxylic acids, esters, and amides on low H2 overvoltage cathodes gives rise to high yields of the respective dihydro compounds, as in the catalytic process, although on metals of high H2 overvoltage reductive dimerization occurs. a,/3-Unsaturated aldehydes and ketones are reduced to a number of products due to the mechanism of reduction. ... [Pg.77]

Alternative Names/Abbreviations 2-Propenoic acid, acroleic acid, ethylene carboxylic acid, vinylformic acid... [Pg.202]

Synonyms AA Acroleic acid Acrylic acid, glacial Ethylene carboxylic acid Propene acid Propenoic acid 2-Propenoic acid Vinylformic acid... [Pg.963]

Ethylenecarboxamide. SeeAcrylamide Ethylene carboxylic acid. See Acrylic acid Ethylene chloride. See Ethylene dichloride Ethylene, chloro-, polymer. See Polyvinyl chloride... [Pg.1110]

Acrylic acids s. a,j3-Ethylene-carboxylic acids Activation s. a. Long-range activation)... [Pg.255]

Acoxy-o,i3-ethylene-carboxylic acid esters Enediolesters... [Pg.286]

X0 compounds 21, 304 Aeridizinium salts 21, 937 Acrylic acids s. a,j -Ethylene-carboxylic acids Acrylonitrile s. Cyanoethylation Activation s a. Functionalization... [Pg.246]

Ethylene carboxylic acid n. A little used Syn acrylic acid. [Pg.372]

Azetidine-2- 1-Aminocyclopropahe- Ethylene carboxylic acid carboxylic acid... [Pg.334]


See other pages where Ethylene carboxylated is mentioned: [Pg.525]    [Pg.265]    [Pg.277]    [Pg.582]    [Pg.71]    [Pg.247]    [Pg.251]    [Pg.257]    [Pg.261]    [Pg.262]    [Pg.269]    [Pg.304]    [Pg.305]    [Pg.345]    [Pg.621]    [Pg.622]    [Pg.207]    [Pg.292]    [Pg.301]    [Pg.319]    [Pg.325]    [Pg.334]   
See also in sourсe #XX -- [ Pg.32 ]




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Carboxylated ethylene copolymers, metal salts

Carboxylated vinyl acetate-ethylene polymer

Carboxylic acid amid ethylene derivs

Carboxylic acid amides from ethylene derivs

Carboxylic acid copolymers ethylene

Copolymers ethylene-carboxylic

Ethylene carboxylation

Ethylene carboxylation

Ethylene derivatives carboxylic acid

Ethylene derivatives carboxylic acid amide

Ethylene derivatives carboxylic acid esters

Ethylene derivs carboxylic acids

Ethylene derivs carboxylic acids, synthesis

Ethylene oxide with carboxyl groups

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