Big Chemical Encyclopedia

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

Articles Figures Tables About

Aliphatic hydrocarbon concentration

Figure 32. Correlation of Fischer assay oil yield with aliphatic hydrocarbon concentration. Key O, %CH=7H(al) and , %CH=H(al) + C(al). (Reproduced, with permission, from Ref. 16.)... Figure 32. Correlation of Fischer assay oil yield with aliphatic hydrocarbon concentration. Key O, %CH=7H(al) and , %CH=H(al) + C(al). (Reproduced, with permission, from Ref. 16.)...
Aliphatic hydrocarbons can be prepared by the reduction of the readily accessible ketones with amalgamated zinc and concentrated hydrochloric acid (Clemmensen method of reduction). This procedure is particularly valuable for the prep>aration of hydrocarbons wdth an odd number of carbon atoms where the Wurtz reaction cannot be applied with the higher hydrocarbons some secondary alcohol is produced, which must be removed by repeated distillation from sodium. [Pg.238]

Chakactkrisation of Unsaturatkd Aliphatic Hydrocarbons Unlike the saturated hydrocarbons, unsaturated aliphatic hydrocarbons are soluble in concentrated sulphuric acid and exhibit characteristic reactions with dUute potassium permanganate solution and with bromine. Nevertheless, no satisfactory derivatives have yet been developed for these hydrocarbons, and their characterisation must therefore be based upon a determination of their physical properties (boiling point, density and refractive index). The physical properties of a number of selected unsaturated hydrocarbons are collected in Table 111,11. [Pg.241]

Peroxides. These are formed by aerial oxidation or by autoxidation of a wide range of organic compounds, including diethyl ether, allyl ethyl ether, allyl phenyl ether, dibenzyl ether, benzyl butyl ether, n-butyl ether, iso-butyl ether, r-butyl ether, dioxane, tetrahydrofuran, olefins, and aromatic and saturated aliphatic hydrocarbons. They accumulate during distillation and can detonate violently on evaporation or distillation when their concentration becomes high. If peroxides are likely to be present materials should be tested for peroxides before distillation (for tests see entry under "Ethers", in Chapter 2). Also, distillation should be discontinued when at least one quarter of the residue is left in the distilling flask. [Pg.5]

The commercial polymers are generally resistant to aqueous acids and alkalis although they are attacked by concentrated sulphuric acid. As might be expected of a highly polar polymer it is not dissolved by aliphatic hydrocarbons but solvents include dimethyl formamide and dimethyl acetamide. [Pg.600]

Nitrile 230 Mineral Oils, Most Aqueous Solutions, Aliphatic Hydrocarbons, Inorganics (at low concentrations and temperatures)... [Pg.43]

The silica gel surface is extremely polar and, as a result, must often be deactivated with a polar solvent such as ethyl acetate, propanol or even methanol. The bulk solvent is usually an n-alkane such as n-heptane and the moderators (the name given to the deactivating agents) are usually added at concentrations ranging from 0.5 to 5% v/v. Silica gel is very effective for separating polarizable materials such as the aromatic hydrocarbons, nitro hydrocarbons (aliphatic and aromatic), aliphatic ethers, aromatic esters, etc. When separating polarizable substances as opposed to substances with permanent dipoles, mixtures of an aliphatic hydrocarbon with a chlorinated hydrocarbon such as chlorobutane or methylene dichloride are often used as the mobile... [Pg.304]

The observations discussed above suggest that the kinetic order of lithium poly-isoprene propagation should vary with the living polymer concentration. The effect is imperceptible in aliphatic hydrocarbons, but is observed in benzene solutions. The apparent propagation constants of lithium polyisoprene (MW 2 2 10 ) were determined in benzene and the results are displayed in Fig. 16 in the form of a plot of log kapp vs log c, c denoting the total living polymer concentration. [Pg.122]

Chemical vapor deposition (CVD) of carbon from propane is the main reaction in the fabrication of the C/C composites [1,2] and the C-SiC functionally graded material [3,4,5]. The carbon deposition rate from propane is high compared with those from other aliphatic hydrocarbons [4]. Propane is rapidly decomposed in the gas phase and various hydrocarbons are formed independently of the film growth in the CVD reactor. The propane concentration distribution is determined by the gas-phase kinetics. The gas-phase reaction model, in addition to the film growth reaction model, is required for the numerical simulation of the CVD reactor for designing and controlling purposes. Therefore, a compact gas-phase reaction model is preferred. The authors proposed the procedure to reduce an elementary reaction model consisting of hundreds of reactions to a compact model objectively [6]. In this study, the procedure is applied to propane pyrolysis for carbon CVD and a compact gas-phase reaction model is built by the proposed procedure and the kinetic parameters are determined from the experimental results. [Pg.217]

Driscoll TR, Hamdan HH, Wang G, et al. 1992. Concentrations of individual serum or plasma bile acids in workers exposed to chlorinated aliphatic hydrocarbons. Br J Ind Med 49 700-705. [Pg.261]

Contaminants in recycled plastic packaging waste (HDPE, PP) were identified by MAE followed by GC-MS analysis [290]. Fragrance and flavour constituents from first usage were detected. Recycled material also contained aliphatic hydrocarbons, branched alkanes and alkenes, which are also found in virgin resins at similar concentration levels. Moreover, aromatic hydrocarbons, probably derived from additives, were found. Postconsumer PET was also analysed by Soxhlet extraction and GC-MS most of the extracted compounds (30) were thermally degraded products of additives and polymers, whereas only a few derived from the original contents... [Pg.467]

From elution chromatography, the percentage of aliphatic hydrocarbons, aromatic hydrocarbons and polar compounds were obtained. The percentage of polar compounds in the oil decreased as the catalyst concentration increased (see Figure 1) with mainly an increase in the percentage of aromatic hydrocarbons. There was also a decrease in the percentage of both acids and bases in the oil as the catalyst concentration increases as shown in Figure 1. [Pg.272]

Several factors indicate that the amino acids detected in all of these carbonaceous chondrites are indigenous and that they must have originated abiotically. First, the presence of protein and non-protein amino acids, with approximately equal quantities of D and L enantiomers points to a nonbiological origin and precludes terrestrial contamination. In addition, the non-extractable fraction of the Murchison is significantly heavier in 13C than terrestrial samples. Finally, the relative abundances of some compounds detected resemble those of products formed in prebiotic synthesis experiments. The aliphatic hydrocarbons are randomly distributed in chain length, and the C2, C3, and C4 amino acids have the highest concentrations (i.e., the most easily synthesized amino acids with the least number of possible structures are most abundant) [4]. [Pg.391]

Spectrofluorimetric methods are applicable to the determination of aliphatic hydrocarbons, and humic and fulvic acids in soil, aliphatic hydrocarbons polyaromatic hydrocarbons, optical whiteners, and selenium in non-saline sediments, aliphatic aromatic and polyaromatic hydrocarbons and humic and fulvic acids in saline sediments. The only application found in luminescence spectroscopy is the determination of polychlorobiphenyl in soil. Generally speaking, concentrations down to the picogram (pg L 1), level can be determined by this technique with recovery efficiencies near f00%. [Pg.26]

Chemical resistance is generally good to limited at room temperature versus dilute bases and weak acids, oils, greases, aliphatic hydrocarbons, and certain alcohols. Resistance is limited to unsatisfactory versus aromatic and halogenated hydrocarbons. Polyesters are attacked by organic and mineral acids, oxidizing agents, concentrated bases, and phenols. [Pg.420]

Polysulfones resist acids at medium concentrations, alcohols, aliphatic hydrocarbons, greases, oils, gasoline, bases, chlorine water. [Pg.541]

Solvents Polysulfones resist acids at medium concentrations, alcohols, aliphatic hydrocarbons, greases, oils, gasoline, chlorine water They are attacked by aromatic hydrocarbons, chlorinated solvents, ketones, esters, phenols, aldehydes, amines Good to limited resistance against oils, greases, aliphatic hydrocarbons, certain alcohols Unsatisfactory against aldehydes, esters, ethers, ketones, aromatic hydrocarbons, chlorinated solvents, amines, certain alcohols, phenols. .. [Pg.641]


See other pages where Aliphatic hydrocarbon concentration is mentioned: [Pg.273]    [Pg.414]    [Pg.273]    [Pg.414]    [Pg.66]    [Pg.67]    [Pg.15]    [Pg.24]    [Pg.607]    [Pg.129]    [Pg.116]    [Pg.382]    [Pg.384]    [Pg.396]    [Pg.447]    [Pg.51]    [Pg.59]    [Pg.105]    [Pg.323]    [Pg.269]    [Pg.390]    [Pg.266]    [Pg.33]    [Pg.262]    [Pg.149]    [Pg.9]    [Pg.9]    [Pg.49]    [Pg.209]    [Pg.630]    [Pg.642]   
See also in sourсe #XX -- [ Pg.252 ]




SEARCH



Aliphatic hydrocarbons

Aliphatic hydrocarbons concentration factor

Hydrocarbon concentration

© 2024 chempedia.info