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Aliphatic/aromatic, separation

Studies on ternary liquid-liquid equilibria have centred on specific challenges facing the chemical, petrochemical, pharmaceutical and biochemical industries. A summary of the ternary liquid-liquid equilibria data (selectivities, capacities) for aliphatic-aromatic separations with ionic hquids is presented in Table 1. The aromatic content (expressed as a percentage) is included to provide an indication of the region in which the selectivity and capacity values are determined (since these are a function of the overall composition). Selectivity and capacity values of traditionally or commercially employed solvents have been included for comparative purposes. The favourable characteristics required for solvents suitable for aromatic-aliphatic separations are the following large selectivity and capacity values, high solubihty of the aromatic components in the ionic hquid, poor solubihty of the ahphatic components in the ionic liquid and the availability of fairly simple and inexpensive means to recover the ionic hquid from the extract and raffinate phases. [Pg.96]

Most of the examples concern substituted diphenyl sulphones, with the anti-leprotic agent 4,4 -diaminodiphenyl sulphone taking a prominent place. Cates and Meloan56 separated aliphatic, aromatic and cyclic sulphones using helium carrier gas and thermal... [Pg.112]

Another variation of the preceding method is to apply HPLC to fractionate the cleaned-up aliphatic-aromatic fraction from flash colurim separation of soluble organic matter as it is performed in the Chevron laboratory, for example, as described in Reference 2. A Waters HPLC system equipped with a preparative Whatman Partisil 10 silica column (9.4 X 500 mm), a HPLC pump, and two detectors for separation monitoring (a UV and refractive index detector) are used, giving three fractions of aliphatic hydrocarbons, mono-, di-, and triaromatics and polar compounds. The hrst two fractions are eluted with hexane, whereas polar compounds are eluted with... [Pg.372]

Figure 13 Combined distillation/pervaporation systems for (a) propylene/ propane splitting and (b) aromatic/aliphatic hydrocarbon separation. (Part a from Ref. 234 part b from Ref. 235.)... Figure 13 Combined distillation/pervaporation systems for (a) propylene/ propane splitting and (b) aromatic/aliphatic hydrocarbon separation. (Part a from Ref. 234 part b from Ref. 235.)...
The solvent extracts can be cleaned up by traditional column chromatography or by solid-phase extraction cartridges. This is a common cleanup method that is widely used in biological, clinical, and environmental sample preparation. More details are presented in Chapter 2. Some examples include the cleanup of pesticide residues and chlorinated hydrocarbons, the separation of nitrogen compounds from hydrocarbons, the separation of aromatic compounds from an aliphatic-aromatic mixture, and similar applications for use with fats, oils, and waxes. This approach provides efficient cleanup of steroids, esters, ketones, glycerides, alkaloids, and carbohydrates as well. Cations, anions, metals, and inorganic compounds are also candidates for this method [7],... [Pg.24]

Imidazo[4,5-c]pyridine (408 R = R = H) and a number of its 2-substituted and 1,2-disubstituted derivatives have been prepared in moderate to good yields by the reaction of the 3,4-diaminopyridines (407) with aliphatic, aromatic and heteroaromatic aldehydes in aqueous alcohol solution in the presence of excess copper(II) acetate in a sealed tube at 130-150 °C (38CB2347, 42CB1936). The Schiff bases (409) are formed primarily in this synthesis, and in many cases it is preferable to isolate the base (409) and effect the subsequent oxidation in a separate operation in alcohol solution. Ring closure of 5-substituted, 6-substituted and 2,6-disubstituted 3,4-diaminopyridines (410) to 7-substituted, 6-substituted... [Pg.639]

Chemical fractionation of whole products and by-products from synthetic fuel production affords a logical first step in the evaluation of these materials for biological activity and the subsequent prediction of health hazards. Aliphatic and aromatic hydrocarbons, along with smaller amounts of heteroatomic species, constitute the bulk of all crude product materials and define a primary class separation need. Subfractionation of these fractions can lead to identification of bioactive components, Aliphatics are separated from the entire sample by a simple liquid chromatographic elution scheme. Aromatic compounds can be isolated by a cyclo-hexane-dimethylsulfoxide solvent partitioning scheme, A Sephadex LH-20 gel separation scheme appears feasible for the fractionation of crude liquids into aliphatic-aromatic, lipophilic-hydrophilic, polymeric, and hydrogen bonding classes of compounds. [Pg.282]

According to literary data, the following mixtures of aromatic/aliphatic-aromatic hydrocarbons were separated toluene/ n-hexane, toluene/n-heptane, toluene/n-octane, toluene/f-octane, benzene/w-hexane, benzene/w-heptane, benzene/toluene, and styrene/ethylbenzene [10,82,83,109-129]. As membrane media, various polymers were used polyetherurethane, poly-esterurethane, polyetherimide, sulfonyl-containing polyimide, ionicaUy cross-linked copolymers of methyl, ethyl, n-butyl acrylate with acrilic acid. For example, when a composite polyetherimide-based membrane was used to separate a toluene (50 wt%)/n-octane mixture, the flux Q of 10 kg pm/m h and the separation factor of 70 were achieved [121]. When a composite mebrane based on sulfonyl-containing polyimide was used to separate a toluene (1 wt%)/ -octane mixture, the flux 2 of 1.1 kg pm/m h and the separation factor of 155 were achieved [10]. When a composite membrane based on ionically cross-linked copolymers of methyl, ethyl, w-butyl acrylate with acrilic acid was used to separate toluene (50 wt%)//-octane mixture, the flux Q of 20-1000 kg pm/m h and the separation factor of 2.5-13 were achieved [126,127]. [Pg.257]

Bitumens, were separated by chromatography, urea clathration and 5A molecular sieve occlusion before and after analyses of many of the aliphatic sub-fractions by GC and gas chromatography-mass spectrometry (GC-MS). Experimental details are noted in a previous publication (16) in which the distribution of cyclic alkanes in two lacustrine deposits of Devonian (N.E. Scotland) and Permian (Autun, France) age, (the D and C series samples) were discussed, Chromatographic separation into aliphatic, aromatic and polar compounds of the bitumens extracted from the shales gave the results shown in Table VI. Carbon Preference Indices and pristane/phytane ratios were measured in this work space limitations precluded... [Pg.73]

Natural Product Reports consists of critical reviews of literature that has been published, during well-defined periods, on the topics of general chemistry and biosynthesis of alkaloids, terpenoids, steroids, fatty acids, and 0-heterocyclic. aliphatic, aromatic and alicyclic natural products. Occasional reviews provide details of techniques for separation and spectroscopic identification, and describe methodologies that are useful to all chemists and biologists actively engaged in the study of natural products. [Pg.637]

The favourable partitioning of the desired solute between the rafiSnate and the extract phases is dependant on the relative affinities (physical interactions) of the solute species for the two phases. This is expressed through a ratio of the distribution coefficients for the separation of an aliphatic-aromatic mixture, partitioning between two phases, known as the selectivity (5) [22], as defined below ... [Pg.90]


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See also in sourсe #XX -- [ Pg.42 ]




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Aliphatic—aromatic

Aromatics separation

Aromatics/aliphatics separation

Aromatics/aliphatics separation

Separations aromatic from aliphatic

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