Big Chemical Encyclopedia

Chemical substances, components, reactions, process design ...

Articles Figures Tables About

Addition hydrocarbons

Optionally, the pH of the aqueous phase of the broken emulsion, after doing the job, can be adjusted to become alkaline. The salts of the polymers are converted into inactive species and the aqueous phase of the broken emulsion can be reinjected into ahydrocarbon-containing formation to recover additional hydrocarbons or bitumen [1187] as an improved oil-recovery process. [Pg.337]

As much as two-thirds of conventional crude oil discovered in U.S. fields remain unproduced, left behind because of the physics of fluid flow. In addition, hydrocarbons in unconventional rocks or that have unconventional characteristics (such as oil in fractured shales, kerogen in oil shale or bitumen in tar sands) constitute an enormous potential domestic supply of energy. [Pg.99]

Additional Hydrocarbon Injection Points Located In various LocaUoni... [Pg.304]

Additionally, vertical fluctuations in the water table due to recovery operations or seasonal variation in precipitation have a direct effect upon the apparent or measured LNAPL thickness (Figure 6.6d). As the water table elevation declines gradually due to seasonal variations, for example, an exaggerated apparent thickness occurs, reflecting the additional hydrocarbon that accumulated in the monitoring well. The same is true for an area undergoing recovery operations where the... [Pg.175]

A subsequent paper (23) gives propagation and termination constants for numerous additional hydrocarbons and deals mostly with relative reactivities of active hydrogen atoms and with effects of structure on termination constants. A comparison of relative reactivities of hydrocarbons toward alkylperoxy, tert-butoxy, and phenyl radicals uses a different alkyl in each alkylperoxy radical in spite of the differences in reactivity among different alkylperoxy (29) radicals. [Pg.55]

Since the work described above was completed, 23 additional hydrocarbons have been brought to cool-flame combustion in the same apparatus (19). Any paraffin, cycloparaffin, or olefin having a research octane number not to exceed 90 may be brought to cool-flame combustion by such a procedure. Aromatic hydrocarbons for the most part do not fall within the indicated range, but n-butyl benzene yields a cool flame with much smoke and soot formation. [Pg.11]

Interpretation of the resulting spectra and comparison with known reference spectra obtained in the same manner confirmed the presence of the substances already identified and allowed us to identify additional hydrocarbons. All constituents of freshly irradiated beef identified during our investigations are summarized in Table IV. [Pg.23]

In any of these tests, different hydrocarbons (such as //-penlane or n-heptane) will give different yields of the asphaltene fraction, and if the presence of the solvent is not compensated by the use of additional hydrocarbon, the yield will be erroneous. In addition, if the hydrocarbon is not present in large excess, the yields of the asphaltene fraction will vary and will be erroneous (Speight, 1999). [Pg.191]

Yoder J. A., Denlinger D. L., Dennis M. W. and Kolattukudy P. E. (1992) Enhancement of diapausing flesh fly puparia with additional hydrocarbons and evidence for alkane biosynthesis by a decarbonylation mechanism. Insect Biochem. Molec. Biol. 22, 237-243. [Pg.252]

In L. humile old reproductive queens also show profiles that differ by almost 50% in the relative abundance of queen-specific compounds from those of workers, which are permanently sterile in this species (de Biseau et al., 2004). In addition, hydrocarbon profiles of virgin non-egg-laying queens are similar to those of workers. However, initiation of egg-laying makes their profiles more like those of mated reproductive queens. [Pg.258]

In the case of methadone and its congeners, the dual diphenyl system (CPh2) does not lead to specially elevated potencies, and it is possible that one phenyl ring serves as a steric restraint for the other in achievement of an active conformation. High orders of activity are found in oripavine derivatives without inclusion of extra aromatic elements, but all potent derivatives have extensive additional hydrocarbon elements attached to the morphine skeleton. [Pg.470]

Shallow geochemical environments consist of solid, aqueous, and air reservoirs and their interfaces. Hydrocarbon compounds partition into these various reservoirs in a manner determined by the stmcture and physical properties of the compounds and the media, and the mechanism of hydrocarbon release. The structure and physical properties of the compounds and media understandably impact their sorption, solubility, volatility, and decomposition behavior (e.g., Schwarzenbach et al., 1993). In addition, hydrocarbon partitioning in real systems is holistically a disequilibrium process hence, the distribution of hydrocarbons depends as much on the pathway taken as on the final physical state of the system (e.g., Schwarzenbach et al., 1993 Luthy et al., 1997). Shallow aquatic systems may tend towards some equilibrium distribution (Figure 10), but this is seldom, if ever, truly attained. [Pg.5025]

The hydrocarbon flux near to the surface varies according to the supply of hydrocarbons and whether local chemical and biological conditions favour their preservation or breakdown. In addition, hydrocarbon magnitudes at any given location vary with time because of displacement by wind, rain and barometric pumping (Wyatt et al., 1995). [Pg.152]

Oudar et al. (69) studied the hydrogenation of butadiene over Pt(l 10), paying special attention to the mechanism of carbon deposition that deactivates the surface. At high hydrogen pressures the rate was first-order in H2 and zero-order in butadiene, but at low H2 pressures the rate became second-order in H2. For high H2, they argued that the surface was covered with one butadiene molecule per two surface Pt atoms and that the sites for butadiene adsorption are different from those for H2 dissociation. At low H2, the sites for H2 dissociation were said to be poisoned by an additional hydrocarbon species. Above a critical temperature, irreversible... [Pg.20]

In addition, hydrocarbons containing tertiary hydrogen atoms may form peroxides as follows ... [Pg.76]


See other pages where Addition hydrocarbons is mentioned: [Pg.63]    [Pg.37]    [Pg.165]    [Pg.269]    [Pg.287]    [Pg.197]    [Pg.344]    [Pg.21]    [Pg.132]    [Pg.403]    [Pg.76]    [Pg.177]    [Pg.332]    [Pg.468]    [Pg.445]    [Pg.293]    [Pg.270]    [Pg.882]    [Pg.365]    [Pg.403]    [Pg.129]    [Pg.213]    [Pg.300]    [Pg.676]    [Pg.2531]    [Pg.25]    [Pg.36]    [Pg.332]    [Pg.533]    [Pg.105]    [Pg.445]   
See also in sourсe #XX -- [ Pg.311 ]




SEARCH



Addition of Other Cations to Hydrocarbons

Addition of halogen to aromatic hydrocarbons

Addition of hydrocarbons

Addition of hydrogen halide to simple unsaturated hydrocarbons

Addition of styrene to aromatic hydrocarbons

Addition reactions unsaturated hydrocarbons

Additional hydrocarbon bridges

Additives brominated hydrocarbons

Additives chlorinated hydrocarbons

Additives reaction with saturated hydrocarbon

Aliphatic hydrocarbons gasoline additives

Aromatic hydrocarbons double-bond addition

Hydrocarbons addition reactions

Hydrocarbons oxidative addition

Hydrocarbons photochemical addition reactions

Hydrocarbons, hydrocarbon synthesis with addition

Hydrocarbons, hydrocarbon with addition

Petroleum Hydrocarbons and Fuel Additives

Self-Ignition of Hydrogenous Mixtures with Hydrocarbon Fuel Additives

Sulfonic acids, addition hydrocarbons

The Reactions of Hydrocarbons Oxidation, Reduction, Substitution, Addition, Elimination, and Rearrangement

© 2024 chempedia.info