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Ethylene water

Ethyl chloride can be dehydrochlorinated to ethylene using alcohoHc potash. Condensation of alcohol with ethyl chloride in this reaction also produces some diethyl ether. Heating to 625°C and subsequent contact with calcium oxide and water at 400—450°C gives ethyl alcohol as the chief product of decomposition. Ethyl chloride yields butane, ethylene, water, and a soHd of unknown composition when heated with metallic magnesium for about six hours in a sealed tube. Ethyl chloride forms regular crystals of a hydrate with water at 0°C (5). Dry ethyl chloride can be used in contact with most common metals in the absence of air up to 200°C. Its oxidation and hydrolysis are slow at ordinary temperatures. Ethyl chloride yields ethyl alcohol, acetaldehyde, and some ethylene in the presence of steam with various catalysts, eg, titanium dioxide and barium chloride. [Pg.2]

Electrochemical Process. Several patents claim that ethylene oxide is produced ia good yields ia addition to faradic quantities of substantially pure hydrogen when water and ethylene react ia an electrochemical cell to form ethylene oxide and hydrogen (206—208). The only raw materials that are utilized ia the ethylene oxide formation are ethylene, water, and electrical energy. The electrolyte is regenerated in situ ie, within the electrolytic cell. The addition of oxygen to the ethylene is activated by a catalyst such as elemental silver or its compounds at the anode or its vicinity (206). The common electrolytes used are water-soluble alkah metal phosphates, borates, sulfates, or chromates at ca 22—25°C (207). The process can be either batch or continuous (see Electrochemicalprocessing). [Pg.461]

The reactions of ethylene, water, and methanol with coadsorbed oxygen on Pdf 100) were studied with temperature programmed reaction spectroscopy (TPRS) and high resolution electron energy loss spectroscopy (EELS). [Pg.165]

The yield based on water could also be calculated but is of no real interest as water is relatively inexpensive compared with ethylene. Water is clearly fed to the reactor in considerable excess. [Pg.49]

In this process, ethylene and water are combined with a recycle stream in the ratio ethylene/water 1/0.6 (mole ratio), a furnace heats the mixture to 300°C, and the gases react over the catalyst of phosphoric acid absorbed on diatomaceous earth. Unreacted reagents are separated and recirculated. By-product acetaldehyde (CH3CHO) is hydrogenated over a catalyst to form more ethyl alcohol. [Pg.612]

Degussa AG Ethanol Ethylene, water Heterogeneous catalysis, high yield and selectivity and low energy costs 8 1984... [Pg.135]

A. Baszkln, L. Ter-Minassian-Saraga, J. Colloid Interface Set 43 (1973) 190 SD, low density poly(ethylene), water trldistilled from permanganate solution in all Pyrex glass apparatus (a) non-oxidlzed, (b) oxidized in a 9.09% KClOs-containlng solution. [Pg.731]

During this first step PdCl2 reacts in a stoichiometric reaction with ethylene, water, and carbon monoxide forming acrylic acid, hydrogen chloride and Pd°. [Pg.169]

Novel H-bond involving aromatic rings have been an important subject in the last decade [4]. The comparison of rr-type H-bond interaction with the traditional water-water o-type H-bond interaction should be very interesting. The interaction energies of ethylene-water tt-H bond and water-water H-bond interactions were calculated to be 2.84 + 0.59 and 4.89 + 0.41 kcal/mol at the MP2/aVDZ level, where the lower and upper limits are the BSSE-corrected and -uncorrected values, respectively. [Pg.158]

Ethylene-o-dichlorobenzene system, 39 Ethylene glycol, 181,182, 327 Ethylene-methanol system, 183 Ethylene-naphthalene system, 69 Ethylene-polyethylene system, 319 Ethylene-n-propanol system, 39 Ethylene-water-organic solvent phase diagrams, 71 Explosives, 347 Extractibility, 367... [Pg.505]

Ethylene-water complex Ethyl formate gauche)... [Pg.1406]

Pressure. Equilibrium is favored by an increase in pressure, and activity is adversely affected. Variations in space velocity and ethylene water ratios may be made to compensate for this decreased catalyst activity however, economic considerations relating to high-pressure equipment lead to an optimum pressure of 1,000 psig. [Pg.791]

The reactions between ethylene, water, and sulfuric acid, in which it was shown the products which may be formed, were given on a previous page and need not be repeated here. Ether is formed according to equilibrium (5), if the external conditions are suitable, and the substances present in suitable concentrations. [Pg.155]

Diffusion Coefficients. Self diffusion coefficients for CO2 (50-52), ethylene ( ), water ( ), and methane ( ) are presented in Figure 16. The critical densities of these fluids are 10.6, 7.8, 17.9, and 10.1 mol/1, respectively. Figure 16 is presented for illustrative purposes only and the references provide a discussion of theoretical considerations and mathematical relationships between density, viscosity, and diffusion. [Pg.21]

Poly [7V-isopropylacrylamide-6-7V-(acetylimino)ethylene] water 2003DAV... [Pg.160]

The reactions of water, alcohols and carboxylic acids with alkenes are explained by these three reaction paths. Formation of acetaldehyde from ethylene, water and PdCb is understood by the sequence of hydroxypalladation to form 5, followed by hydride shift. It has been confirmed that no incorporation of deuterium occurs by the reaction of ethylene with PdCl2 carried out in D2O, and the four hydrogens in ethylene are retained in acetaldehyde, indicating that hydride shift occurs (path c) [1]. Therefore, free vinyl alcohol (6), expected to be formed by )3-H elimination (path a), is not an intermediate (path c). In the presence of LiCl, 2-chloroethanol (7) is obtained by path b. [Pg.30]


See other pages where Ethylene water is mentioned: [Pg.203]    [Pg.208]    [Pg.406]    [Pg.170]    [Pg.170]    [Pg.203]    [Pg.208]    [Pg.98]    [Pg.140]    [Pg.96]    [Pg.33]    [Pg.210]    [Pg.215]    [Pg.406]    [Pg.64]    [Pg.97]    [Pg.187]    [Pg.71]    [Pg.341]    [Pg.32]    [Pg.187]    [Pg.123]    [Pg.406]    [Pg.212]    [Pg.199]    [Pg.204]    [Pg.848]    [Pg.849]   
See also in sourсe #XX -- [ Pg.41 ]

See also in sourсe #XX -- [ Pg.41 ]




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Addition of water to ethylenic bonds

Ethylene glycol in water

Ethylene glycol mixtures with water

Ethylene glycol with water

Ethylene glycol-water mixtures, freezing

Ethylene glycol-water mixtures, freezing point

Ethylene glycol-water, efficiency

Ethylene oxide by water

Ethylene reaction with water

Surface water ethylene concentrations

Water Solubility of Ethylene Glycol n-Butyl Ether

Water Vapor Dew Points Over Aqueous Ethylene Glycol Solutions

Water dissolving ethylene glycol

Water ethylene glycol

Water-ethylene glycol catalyst

Water-ethylene glycol mixtures

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