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Ahcyclic hydrocarbons

Binary blends prepared by mixing iPP with a fully saturated ahcyclic hydrocarbon resin (obtained by cationic oligomerization of indene, a-methyl styrene, and vinyl toluene, followed by hydrogenation) showed good miscibihty in the melt state (12). [Pg.122]

Rios-Hemandez L. A., Gieg L. M., and Suflita J. M. (2003) Biodegradation of an ahcyclic hydrocarbon by a sulfate-reducing emrichment from a gas condensate-contaminated aquifer. Appl. Environ. Microbiol. 69(1), 434-443. [Pg.473]

Thus, the permeation of hydrocarbons in polymer membranes is governed by the basic regularities typical of permeation of low MW penetrants, modified however by certain peculiarities related to the stmcture and shape of hydrocarbon molecules. We will now discuss the physicochemical regularities of hydrocarbon separation and removal using polymer membranes, by trying to reveal the relationship between the chemical stmcture of polymers and their separation properties with respect to mixtures containing hydrocarbons. It follows from literary data that mbbery polymers are mainly used in gas/vapor separation processes for selective separation of hydrocarbon vapors from their mixtures with air as well as in pervaporation processes for the removal of hydrocarbons from their aqueous solutions. In practice, glassy polymers are used for separation of olefins and paraffins as well as for separation of aromatic, ahcyclic, and aliphatic hydrocarbons. [Pg.240]

Isolated compounds include alkyl, aromatic, ahcyclic, or functional groups with significant hydrocarbon structure. All isolates have a potential for nonpolar interaction (except inorganic ions and compounds with polar groups, e.g., carbohydrates). Because of this fact, the nonpolar interactions are nonselective and allow the extraction of... [Pg.1404]

Handa, Y. P. Benson, G. C. Thermodynamic properties of binary hquid mixtures involving weak specific interactions. Part III. Excess enthalpies of binary mixtures of tetrachloromethane and tetrachloroethene with some ahcyclic, pseudoaromatic, and aromatic hydrocarbons at 298.15 K Fluid Phase Equilib. 1980,4, 277-285... [Pg.563]


See other pages where Ahcyclic hydrocarbons is mentioned: [Pg.4999]    [Pg.262]    [Pg.26]    [Pg.4999]    [Pg.262]    [Pg.26]    [Pg.736]    [Pg.533]   
See also in sourсe #XX -- [ Pg.77 ]




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