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Carbon ethylene

Ziegler found that adding certain metals or their compounds to the reaction mixture led to the formation of ethylene oligomers with 6-18 carbons but others promoted the for matron of very long carbon chains giving polyethylene Both were major discoveries The 6-18 carbon ethylene oligomers constitute a class of industrial organic chemicals known as linear a olefins that are produced at a rate of 3 X 10 pounds/year m the... [Pg.610]

Fig. 4.3 b. The changes in the LU partial population of pt orbital at -carbon ethylene-chlorine cation system... [Pg.33]

Water is involved in most of the photodecomposition reactions. Hence, nonaqueous electrolytes such as methanol, ethanol, N,N-d i methyl forma mide, acetonitrile, propylene carbonate, ethylene glycol, tetrahydrofuran, nitromethane, benzonitrile, and molten salts such as A1C13-butyl pyridium chloride are chosen. The efficiency of early cells prepared with nonaqueous solvents such as methanol and acetonitrile were low because of the high resistivity of the electrolyte, limited solubility of the redox species, and poor bulk and surface properties of the semiconductor. Recently, reasonably efficient and fairly stable cells have been prepared with nonaqueous electrolytes with a proper design of the electrolyte redox couple and by careful control of the material and surface properties [7], Results with single-crystal semiconductor electrodes can be obtained from table 2 in Ref. 15. Unfortunately, the efficiencies and stabilities achieved cannot justify the use of singlecrystal materials. Table 2 in Ref. 15 summarizes the results of liquid junction solar cells prepared with polycrystalline and thin-film semiconductors [15]. As can be seen the efficiencies are fair. Thin films provide several advantages over bulk materials. Despite these possibilities, the actual efficiencies of solid-state polycrystalline thin-film PV solar cells exceed those obtained with electrochemical PV cells [22,23]. [Pg.233]

Method E (t-butyl esters of peptides and amino acids) K2CO, (36 g) is added to the amino acid (10 mmol) and TEBA-C1 (2.28 g, 10 mmol) in MeCONMe2 (75 ml) at room temperature. Me,CBr (65.75 g, 0.48 mol) is then added and the mixture is stirred at 55 °C for 24 h. H20 (1000 ml) is added to the cooled mixture and the precipitated material is collected and extracted with EtOAc (250 ml). The extract is washed with H20 (2 x 100 ml), dried (Na2S04), and evaporated to yield the /-butyl ester (80-100%) Method F (from ethylene carbonates) Ethylene carbonate (2 g, 22 mmol), the carboxylic... [Pg.88]

By Pyrolysis f Certain Thiolcarbovatee and I-Mercafnoalkyl Carbonates Ethylene monothiolcarbonate (X), ethyl 2-hydroxyethylthiol-carbonate (XI), and ethyl 2-meroaptoethyloarbonate (XU) are readily pyrolyzed to yield ethylene sulfide.84 At atmospheric pressure (X) ch, —cnB o o... [Pg.297]

Glycols have two or more hydroxyl groups on adjacent carbons. Ethylene glycol, glycerol, and sorbitol are examples of glycols that are commercially important. Three important industrial alcohols are methanol, ethanol, and 2-propanol. [Pg.123]

Finely divided platinum induces no effect with acetylene at ordinary temperatures, but above 150° intumescence is observed, and the gas is partly decomposed into carbon, ethylene, benzene, ethane, and hydrogen, the last three in small quantity. [Pg.93]

DBU DMC DMF EC EO EOS GSS ILs MBMTBP MEA MW PC PDMS PEG PEGda PEO PMPS PO PPG PPGda PTC PTHF PTMO PVP Diazabicyclo[5.4.0] -undec-7-ene Dimethylcarbonate Dimethylform amide Ethylene carbonate Ethylene oxide, oxyethylene Equation of state Gas-saturated solution Ionic liquids 2,2,-methylene-bis(4-methyl-6-tert-butylphenol) Monoethanolamine Molecular weight Propylene carbonate Polydimethylsiloxane Polyethylene glycol Poly(ethylene glycol) diacrylate Polyethylene oxide Poly(methylphenylsiloxane) Propylene oxide Poly(propylene glycol) Poly(propylene glycol) diacrylate Phase-transfer catalyst Poly(tetrahydrofuran) Polytetramethylene oxide Polyvinyl pyrrolidone... [Pg.1]

Butanone y-butyrolactone Diethyl carbonate Diethyl sulfite Dimethylcarbonate Ethyl acetate Ethyl formate Ethylene carbonate Ethylene glycol sulfite Methyl acetate Methyl formate Nitromethane... [Pg.76]

Methane Ethene Carbon (Ethylene) dioxide Ethyne (Acetylene) Ammonia Nitrous acid Hydrogen cyanide Water Formaldehyde... [Pg.3]

Athene carbonates. Ethylene carbonate (I) is formed when ethylene oxide and carbon dioxide are heated at 100° in benzene solution containing this nickel(0) complex. Under similar conditions, 2-methyl-1,2-epoxypropane is converted into 1,1-dimethyl-ethylene carbonate and 2,3-epoxybutanc into 1,2-dimethylethylene carbonate. Several other catalysts of the type L2Ni(0) are effective. [Pg.41]

Useful solvents must themselves resist oxidation or reduction, should dissolve suitable ionic solutes and nonelectrolytes, and in addition should be inexpensive and obtainable in high purity. Kratochvil indicated that the most potentially useful solvents are those that have a dielectric constant greater than about 25 and have Lewis-base properties. Some solvents meeting these criteria are acetonitrile, dimethyl-sulfoxide, dimethylformamide, dimethylacetamide, propylene carbonate, ethylene carbonate, formamide, sulfolane, and y-butyrolactone. Solvents of the Lewis-base type show specific solvation effects with many metal cations (Lewis acids). Thus acetonitrile functions as a Lewis base toward the silver ion. At the same time it reacts but little with the hydrogen ion. [Pg.294]

A great variety of bases has been used to generate ylides from the corresponding phosphonium salts various nitrogen bases, alkoxides, alkali metal hydrides, carbanionic bases, alkali metal hydroxides and carbonates, ethylene oxides, basic ylides and others. ... [Pg.174]

Ai3-18365 Carbonic acid, cyclic ethylene ester CCRIS 293 Cyclic ethylene carbonate Dioxolone-2 EINECS 202-510-0 Ethylene carbonate Ethylene carbonic acid Ethylene glycol carbonate Ethylene glycol, cyclic carbonate Ethylenester kyseiiny uhlicite Glycol carbonate HSDB 6803 NSC 11801 Texacat EC. Solvent for organic and Inorganic material ERA Rule 66 exempt also used as reactant and plasticizer in fibers and textiles, plastics and resins, aromatic hydrocarbon extraction, electrolytes, hydraulic brake fluids. Plates mp = 36.4" bp = 248° = 1,3214 freely soluble in H2O,... [Pg.270]

These blends are commercially available, e.g., Zytel 3100 , Grilon BT. They show improved processability, solvent resistance, elongation, low-temperature impact and tensile strength, as well as enhanced barrier properties (see Table 1.56). They have been also incorporated into more complex, multicomponent systems, e.g., PA/PARA = 1 1, PPE, PCL, ionomer, EPR, a monomeric mixture of oxide and/or carbonate [e.g., ethylene carbonate, ethylene oxide, etc.] and a polyhydric alcohol [e.g., ethylene glycol, or trimethylene glycol]. The alloys were used to mold parts for the automotive, electrical or electronic industries [Hamada et al., 1994],... [Pg.64]

Ethoxybenzene 2-Ethoxyethanol 2-Ethoxyethyl acetate Ethyl acetate Ethyl acrylate Ethylamine gauche) Ethylamine trans) Ethylamine average) Ethylbenzene Ethyl benzoate Ethyl butanoate Ethyl ra 5-cinnamate Ethyl cyanate Ethyl cyanoacetate Ethylene carbonate Ethylene glycol average) Ethyleneimine Ethylene-sulfur dioxide complex... [Pg.1406]

Attack on Saturated Carbon. - Ethylene dicarboxylic diphosphonic acid (EDCP, 2) has been prepared in 70% yield from 2,3-dichlorosuccinic anhydride (3) and trimethyl phosphite, followed by hydrolysis of the Arbuzov product. Tris(trimethylsilyl) phosphite, in contrast to trialkyl phosphites, attacks an oxirane carbon of epibalohydrins (4) to give the phosphonates (5). Bis(trimethylsilyl) phosphonite (6) has previously been prepared in situ and used to obtain y-ketophosphinic acids similar reactions with simple alkyl halides to give alkylphosphinic and dialkylphosphinic acids acids in high yields have now been described. ... [Pg.81]


See other pages where Carbon ethylene is mentioned: [Pg.98]    [Pg.87]    [Pg.191]    [Pg.214]    [Pg.195]    [Pg.116]    [Pg.3]    [Pg.665]    [Pg.209]    [Pg.909]    [Pg.911]    [Pg.88]    [Pg.410]    [Pg.216]    [Pg.569]    [Pg.134]    [Pg.261]    [Pg.195]    [Pg.361]    [Pg.88]    [Pg.179]    [Pg.309]    [Pg.569]    [Pg.143]    [Pg.50]    [Pg.61]    [Pg.402]    [Pg.634]    [Pg.444]    [Pg.90]   
See also in sourсe #XX -- [ Pg.162 , Pg.163 , Pg.164 ]




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Alternating copolymerization, ethylene with carbon monoxide

Carbon bisulfide, reaction with ethylene

Carbon disulfide reaction with ethylene diamine

Carbon monoxide/ethylene copolymerization

Carbon monoxide/ethylene decomposition

Carbon monoxide/ethylene mechanism

Carbon-1 3 from ethylene-1-olefin

Carbonic acid anhydrides ethylene derivatives

Copolymers ethylene-carbon monoxide

EBCO ethylene-n-butyl acrylate-carbon monoxide terpolymer

Ethylene carbon charge

Ethylene carbonate

Ethylene carbonate

Ethylene carbonate 7?)-ethyl lactate

Ethylene carbonate capacity measurements

Ethylene carbonate electrolytes

Ethylene carbonate, reaction with potassium thiocyanate

Ethylene lithiated carbons

Ethylene oxide -carbon dioxide mixture

Ethylene oxide -carbon dioxide mixture sterilization

Ethylene oxide reaction with carbon dioxide

Ethylene reactions with carbon dioxide

Ethylene three carbon atom products from

Ethylene vinyl acetate carbon monoxide products

Ethylene, carbon layers

Ethylene, carbon layers surface

Ethylene-carbon monoxide

Ethylene-carbon monoxide copolymers (ECO)

Ethylene-carbon monoxide degradation

Ethylene-carbon monoxide effects

Ethylene-carbon monoxide physical properties

Ethylene-carbon monoxide polymerization

Ethylene-carbon monoxide polymers

Ethylene-carbon monoxide products

Ethylene-carbon monoxide recycling

Ethylene-carbon monoxide temperature effects

Ethylene-co-carbon monoxide

Ethylene/propylene/carbon monoxide

Ethylene/propylene/carbon monoxide terpolymers

Fluoro-ethylene carbonate

Furan with ethylene carbonate

Hydrogen Carbon dioxide Ethylene

Initiation ethylene/carbon monoxide

Litter ethylene-carbon monoxide copolymer

Methylene ethylene carbonate

Molecular weight ethylene-carbon monoxide

Oxidation carbon monoxide, ethylene

Photodegradation ethylene-carbon monoxide copolymers

Poly(ethylene-co-carbon monoxide

Polyethylene and ethylene-carbon monoxide

Propagation ethylene/carbon monoxide

Solvents ethylene carbonate

Supercritical ethylene carbonate

Temperature ethylene-carbon monoxide copolymers

Vinyl ethylene carbonate

Vinyle ethylene carbonate

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