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Ethylene peroxide from

Low Temperature Reaction. Reaction in the low temperature regime below 320°C. is of a different character. The products include carbon dioxide and significant quantities of peroxy compounds, as well as carbon monoxide, water, formaldehyde, and methanol, but methane and ethylene are formed only in traces. The peroxy compounds comprise hydrogen peroxide from all three ketones, methyl hydroperoxide from acetone (8) and methyl ethyl ketone (I), and ethyl hydroperoxide from diethyl ketone (1). Methyl ethyl ketone also gives large amounts of peracetic acid (1). [Pg.108]

Hydrogen peroxide f/Y7 5-Ethylene derivs. from selenides s. 31, 813... [Pg.578]

By far the greatest part of PVC production across the world is now made by the suspension process. Vinyl chloride monomer (derived from a reaction between ethylene (derived from oil) and chlorine (derived from common salt) is dispersed in deionised water with the help of small quantities of chemical dispersants and polymerisation initiators (typically peroxide compounds). At moderately raised temperature (50 C) and pressure (0.7 MPa) polymerisation proceeds and the polymer can be removed from the resulting slurry by de-watering and steam stripping the unconverted vinyl chloride monomer. [Pg.22]

This type of reaction has been recognized in the decomposition of peroxi-dized linolenic acid. The application of olive oil to hasten the enlargement and maturation of fig fruits has been practiced predating Christianity, and it is now clear that this effect is due to the action of ethylene derived from the degradation of olive oil (Saad et al., 1969). Linolenic acid was once suggested as a precursor of ethylene, based on the observation that peroxidized... [Pg.164]

Mercuration-demercuration Unsym. peroxides from ethylene derivs. [Pg.352]

Hydrogen peroxide Ethylene derivs. from selenides... [Pg.539]

Hydrogen peroxide/sodium carbonate Sym. ethylene deriTS. from 2-alkylidenephosphorane molecules Carotinoids... [Pg.510]

Trimethylamine, CjH N, (CH3J3N. Colourless liquid with a strong fishy odour, miscible with water, m.p. — I24 C, b.p. 3-5°C. It occurs naturally in plants, herring brine, bone oil and urine. It reacts with hydrogen peroxide to give trimethylamine oxide and with ethylene oxide to give choline its commercial importance stems chiefly from this latter reaction. [Pg.260]

Ethylene-propylene-diene rubber is polymerized from 60 parts ethylene, 40 parts propylene, and a small amount of nonconjugated diene. The nonconjugated diene permits sulfur vulcanization of the polymer instead of using peroxide. [Pg.1064]

The changeover from ROO radicals to HOO radicals and the switch from organic peroxides to HOOH has been shown as temperature is increased in propane VPO (87,141). Tracer experiments have been used to explore product sequences in propane VPO (142—145). Propylene oxide comes exclusively from propylene. Ethylene, acetaldehyde, formaldehyde, methanol, carbon monoxide, and carbon dioxide come from both propane and propylene. Ethanol comes exclusively from propane. [Pg.341]

Vinyl Acetate—Ethylene Copolymers. In these random copolymers, the ratio of ethylene to vinyl acetate (EVA) is varied from 30—60%. As the vinyl acetate content increases, the oil and heat resistance increases. With higher ethylene content the physical strength, tensile, and tear increases. The polymers are cured with peroxide. The main properties of these elastomers include heat resistance, moderate oil and solvent resistance, low compression set, good weather resistance, high damping, exceUent o2one resistance, and they can be easily colored (see Vinyl polymers, poly(VINYL acetate)). [Pg.234]

Carbon tetrachloride forms telomers with ethylene and certain other olefins (14—16). The mixture of Hquid products derived from ethylene telomerization may be represented CCl2(CH2CH2) Cl ia which nis 2l small number. Reaction of ethylene and carbon tetrachloride takes place under pressure and is induced by the presence of a peroxygen compound, eg, ben2oyl peroxide (17—19) or metal carbonyls (14,15). [Pg.531]

The most widely used plasticizers are paraffinic oils. Por appHcations that specify high use temperatures, or for peroxide cures, paraffinic oils of low volatihty are definitely recommended. However, since paraffinic oils exude at low temperatures from EPDM vulcanizates, or from high ethylene EPDMs, they are often blended with naphthenic oils. On the other hand, naphthenic oils interfere with peroxide cures. Aromatic oils reduce the mechanical properties of vulcanizates, and they also interfere with peroxide cures. Therefore, they are not recommended for EPM/EPDM. [Pg.504]

Isopropyl Ether. Isopropyl ether is manufactured by the dehydration of isopropyl alcohol with sulfuric acid. It is obtained in large quantities as a by-product in the manufacture of isopropyl alcohol from propylene by the sulfuric acid process, very similar to the production of ethyl ether from ethylene. Isopropyl ether is of moderate importance as an industrial solvent, since its boiling point Hes between that of ethyl ether and acetone. Isopropyl ether very readily forms hazardous peroxides and hydroperoxides, much more so than other ethers. However, this tendency can be controlled with commercial antioxidant additives. Therefore, it is also being promoted as another possible ether to be used in gasoline (33). [Pg.429]

Diethylene glycol monoethyl ether [111-90-0] M 134.2, b 201.9", d 0.999, n 1.4273, n 1.4254. Ethylene glycol can be removed by extracting 250g in 750mL of benzene with 5mL portions of water, allowing for phase separation, until successive aqueous portions show the same volume increase. Dried, and freed from peroxides, as described for diethylene glycol mono-n-butyl ether. [Pg.203]

Ethylene-vinyl acetate copolymers have been available for several years from Bayer (Levapren 450) and these contain about 45% of vinyl acetate units. As with EPM these rubbers cannot be cured with accelerated sulphur systems but by peroxides. [Pg.301]

Tetrahydrofuran may be purified by refluxing over solid potassium hydroxide, followed by distillation from lithium alu-miniun hydride. Tetrahydrofuran may be replaced by ethylene glycol dimethyl ether (dimethoxyethane). The submitter has indicated that either solvent may be freed conveniently from water, alcohols, and moderate amounts of peroxides by passing the commercial solvent through a column (2 in. diameter X 2-3 ft. length) of Linde Air Products Molecular Sieves (type 13A iQ- n. pellets), at a rate of approximately 100 ml. per minute. [Pg.32]

I Initiation The polymerization reaction is initiated when a few radicals are generated on heating a small amount of benzoyl peroxide catalyst to break the weak 0-0 bond. A benzoyloxy radical then adds to the C=C bond of ethylene to generate a carbon radical. One electron from the C=C bond pairs up with the odd electron on the benzoyloxy radical to form a C-O bond, and the other election remains on carbon. [Pg.240]

Introduction of fluorine by oxirane-ring opening is described first. The 1,2-oxirane 408, prepared from nitroalkene 407 and hydrogen peroxide, was treated with KHF2 (ethylene glycol, 20 min, 112°) to 2-... [Pg.155]


See other pages where Ethylene peroxide from is mentioned: [Pg.48]    [Pg.171]    [Pg.346]    [Pg.327]    [Pg.168]    [Pg.84]    [Pg.604]    [Pg.347]    [Pg.886]    [Pg.300]    [Pg.413]    [Pg.308]    [Pg.124]    [Pg.47]    [Pg.208]    [Pg.184]    [Pg.238]    [Pg.239]    [Pg.440]    [Pg.484]    [Pg.235]    [Pg.194]    [Pg.112]    [Pg.81]    [Pg.766]    [Pg.305]    [Pg.357]    [Pg.210]    [Pg.170]    [Pg.869]    [Pg.105]    [Pg.149]   
See also in sourсe #XX -- [ Pg.273 ]




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