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Hydrocarbon alcohol

Chemical Properties. A combination of excellent chemical and mechanical properties at elevated temperatures result in high performance service in the chemical processing industry. Teflon PEA resins have been exposed to a variety of organic and inorganic compounds commonly encountered in chemical service (26). They are not attacked by inorganic acids, bases, halogens, metal salt solutions, organic acids, and anhydrides. Aromatic and ahphatic hydrocarbons, alcohols, aldehydes, ketones, ethers, amines, esters, chlorinated compounds, and other polymer solvents have Httle effect. However, like other perfluorinated polymers,they react with alkah metals and elemental fluorine. [Pg.375]

Autooxidation. Liquid-phase oxidation of hydrocarbons, alcohols, and aldehydes by oxygen produces chemiluminescence in quantum yields of 10 to 10 ° ein/mol (128—130). Although the efficiency is low, the chemiluminescent reaction is important because it provides an easy tool for study of the kinetics and properties of autooxidation reactions including industrially important processes (128,131). The light is derived from combination of peroxyl radicals (132), which are primarily responsible for the propagation and termination of the autooxidation chain reaction. The chemiluminescent termination step for secondary peroxy radicals is as follows ... [Pg.269]

Most organic compounds, including aromatic hydrocarbons, alcohols, esters, ketones, ethers, and carboxyUc acids are miscible with nitroparaffins, whereas alkanes and cycloalkanes have limited solubiUty. The lower nitroparaffins are excellent solvents for coating materials, waxes, resins, gums, and dyes. [Pg.98]

Carbon disulfide is completely miscible with many hydrocarbons, alcohols, and chlorinated hydrocarbons (9,13). Phosphoms (14) and sulfur are very soluble in carbon disulfide. Sulfur reaches a maximum solubiUty of 63% S at the 60°C atmospheric boiling point of the solution (15). SolubiUty data for carbon disulfide in Hquid sulfur at a CS2 partial pressure of 101 kPa (1 atm) and a phase diagram for the sulfur—carbon disulfide system have been published (16). Vapor—Hquid equiHbrium and freezing point data ate available for several binary mixtures containing carbon disulfide (9). [Pg.27]

Polydiethylene glycol succinate 50-200° Aromatic hydrocarbons, alcohols, ketones, esters. [Pg.39]

The chemical resistance of the linear polymers is also very good. Resistant to most acids, aqueous bases, hydrocarbons, most halogenated hydrocarbons, alcohols and phenols, they are attacked by concentrated sulphuric acid, formic acid, some amines, benzaldehyde, nitromethane and a few other reagents. They will dissolve in 1-chloronaphthalene at elevated temperatures but in general have excellent solvent resistance. The polymer is cross-linked by air oxidation at elevated temperatures. [Pg.594]

CFCs have been widely used as cleaning solvents, as they are nonflammable and their toxicity is low. Now, flammable solvents are coming back into favor. A news item from a manufacturer described "a new ozone-friendly cleaning process for the electronics industry, which "uses a unique hydrocarbon-alcohol formulation. It did not remind readers that the mixture is flammable and that they should check that their equipment and procedures are suitable. [Pg.71]

Waxes are water-repelling solids that are part of the protective coatings of a number of living things, including the leaves of plants, the fur of animals, and the feathers of birds. They are usually mixtures of esters in which both the alkyl and acyl group are unbranched and contain a dozen or more carbon atoms. Beeswax, for example, contains the ester triacontyl hexadecanoate as one component of a complex mixture of hydrocarbons, alcohols, and esters. [Pg.1079]

The methods of analysis of polymer additives and chemicals, such as hydrocarbons, alcohols, etc., are not only restricted to the field of polymer chemistry but can also be applied for the analysis of such materials in the field of food chemistry. In addition, the analysis of polyaromatic hydrocarbons in edible oils has been of extreme importance. Polymeric packaging materials that are intended for food-contact use may contain certain additives that can migrate into the food products which are actually packaged in such products. The amounts of the additives that are permitted to migrate into food samples are controlled by government agencies in order to show... [Pg.305]

In the Fischer-Tropsch process, carbon monoxide reacts with hydrogen in the presence of a solid catalyst, with the formation of a mixture of hydrocarbons. The composition of the product varies considerably with the catalyst and the operating conditions. The mixture may include (in addition to hydrocarbons) alcohols, aldehydes, ketones, and acids. [Pg.76]

The names of organic compounds are based on the names of the parent hydrocarbons alcohols contain —OH groups, carboxylic acids contain —COOH groups, and haloalkanes contain halogen atoms. [Pg.60]

Deposition Precursors. Diamond has been deposited from a large variety of precursors which include, besides methane, aliphatic and aromatic hydrocarbons, alcohols, ketones, and solid polymers such as polyethylene, polypropylene, and polystyrene, and halogens. [Pg.197]

The Grignard reagents prepared from the activated magnesium appear to react normally with electrophiles. Thus reactions with proton donors, ketones, and carbon dioxide afford hydrocarbons, alcohols, and carboxylic acids, respectively. The reductive coupling of ketones to pinacols had also been accomplished with the activated magnesium. ... [Pg.47]

In fact, fluorinated polyphosphazenes are usually considered to be extremely stable towards chemical agents and aggressives due to the presence of C-F bonds in the side phosphorus substituents. PTFEP, for instance, appears to be completely insensitive to several, most common, solvents (aliphatic and aromatic hydrocarbons, alcohols and water), to acids (e.g. acetic acid), and to bases (e.g. pyridine and concentrated NaOH solutions), although some decomposition could be observed in triethylamine and in concentrated H2SO4 [41]. Phos-phazene fluoroelastomers, moreover, are known to be completely insoluble in aromatic solvents [533] and petroleum-resistant materials [502-506,552]. [Pg.198]

Polyesters are, in general, organic solvent resistant. They show excellent room temperature resistance to organic solvents, such as hydrocarbons, alcohols, and chlorinated hydrocarbons. At slightly elevated temperatures of approximately 60 °C, alcohols and aromatic solvents can damage the polymer. Strong acids and bases can cause chemical damage to polyesters, as can ketones and phenols. [Pg.379]

Shiu, W.Y., Mackay, D. (1997) Henry s law constants of selected aromatic hydrocarbons, alcohols, and ketones. J. Chem. Eng. Data 42, 27-30. [Pg.915]

Many volatile organic compounds (hydrocarbons, alcohols, aldehydes, acids, esters, ketones, amines, etc.) have been identified in marine systems [ 156,157]. These volatile materials may have an important role in the cycling of organic... [Pg.503]

The nature of the catalysts, especially those formed in situ from chlo-rorhodium(I) precursors, deserves some comment. The catalysts have been often written as Rh(P )2Cl(solvent), where P and (P )2 represent monodentate and bidentate chiral phosphines, respectively (10), but this almost certainly pertains for nonpolar media only. In polar media, including the mixed hydrocarbon/alcohol solvents usually employed,... [Pg.351]

Co-Oxidation of Aldehydes with Hydrocarbons, Alcohols, and Aldehydes... [Pg.9]

Although this classic picture evolved from "soft, mononuclear transition metal complexes suffices to explain a great deal of carbon monoxide chemistry, it is not clear that it is complete or accurate for understanding processes whereby CO is reduced, deoxygenated, and/or polymerized to form methane, long-chain hydrocarbons, alcohols, and other oxocarbons, especially in cases where heterogeneous catalysts or "hard" metals are involved (6, 7, ,9,J 0). This deficiency of information has led to the search for new modes of carbon monoxide reactivity and to attempts to understand carbon monoxide chemistry in nontraditional environments ... [Pg.59]


See other pages where Hydrocarbon alcohol is mentioned: [Pg.1045]    [Pg.297]    [Pg.70]    [Pg.101]    [Pg.725]    [Pg.1115]    [Pg.208]    [Pg.587]    [Pg.276]    [Pg.1045]    [Pg.206]    [Pg.103]    [Pg.278]    [Pg.15]    [Pg.147]    [Pg.147]    [Pg.147]    [Pg.147]    [Pg.119]    [Pg.419]    [Pg.429]    [Pg.1581]    [Pg.57]    [Pg.20]    [Pg.37]    [Pg.20]    [Pg.349]    [Pg.249]    [Pg.104]   
See also in sourсe #XX -- [ Pg.76 , Pg.77 , Pg.78 , Pg.79 , Pg.80 , Pg.184 ]

See also in sourсe #XX -- [ Pg.1037 , Pg.1038 , Pg.1039 ]




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Hydrocarbons, hydrocarbon alcohols

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