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Alcohols adsorption processing

Decisive role of the VM factor during the adsorption process of the solvents by coal is in agreement with the determined in the work [25] proportionality for the alcohols between Igk and steric factor Es of the Hammet-Taft s equation. [Pg.61]

All adsorption processes result from the attraction between like and unlike molecules. For the ethanol-water example given above, the attraction between water molecules is greater than between molecules of water and ethanol As a consequence, there is a tendency for the ethanol molecules to be expelled from the bulk of the solution and to concentrate at die surface. This tendency increases with the hydrocarhon chain-length of the alcohol. Gas molecules adsorb on a solid surface because of die attraction between unlike molecules. The attraction between like and unlike molecules arises from a variety of intermolecular forces. London dispersion forces exist in all types of matter and always act as an attractive force between adjacent atoms and molecules, no matter how dissimilar they are. Many oilier attractive forces depend upon die specific chemical nature of the neighboring molecules. These include dipole interactions, the hydrogen bond and the metallic bond. [Pg.1581]

To obtain individual phospholipids of greater than 50-60% purity, some form of selective adsorption process is usually required. Adsorption and distribution chromatography present these options. Treatment of the alcohol-soluble lecithin with alumina yields a fraction very rich in phosphatidylcholine and free of phosphatidylethanolamine and phosphatidylinositol (167). Although these products are available only in very limited quantities for highly specialized markets, products such as a lecithin containing up to 95% PC can be obtained commercially. [Pg.1757]

Polar solvents inhibit the reaction, presumably by interfering with the adsorption process as noted in the mechanism proposed for manganese dioxide oxidations. Oxidation of 1-heptanol to heptanal with Fetizon s reagent was quantitative when the solvent was 35% hexanes. When benzene was used as a solvent, the yield of heptanal dropped to 90% and was < 1% in ethyl acetate, methyl ethyl ketone, or acetonitrile. 69 Since the oxidation is a heterogeneous reaction, requiring adsorption of the alcohol substrate, as the surface area of the reagent increases (increased by precipitation on Celite), the rate of oxidation increases. An optimum ratio is reached beyond which increasing the silver carbonate/Celite ratio slows the oxidation. 69... [Pg.217]

The inference is that vacuum treatment has removed blocking molecules from the limited number of nanopores in the unactivated carbon and allowed ingress of deuterated water. Shifts to lower frequencies of adsorbates have been noted for alcohols adsorbed on carbon and have been assigned to the shielding effects of the graphene planes (Harris et al. 1995). These shifts to lower frequency are thus indicative of adsorption processes occurring in the pore system within the bulk of the adsorbent material. [Pg.465]

Anti-wear performance of adsorbates is only one step removed from their action as corrosive agents. This is exemplified by the action of stearic acid on copper surfaces which rapidly produce reaction products after initial absorption. This also applies to alcohols which adsorb strongly on an iron surface activated by milling in a dilute solution of stearic acid in n-heptane in the absence of O2. The adsorption is followed by a chemical reaction characterised by a steady heat evolution after completion of the adsorption process (15]. [Pg.170]

Lewis acid sites can adsorb water as any other molecules having some amount of basicity. As discussed in the case of alcohol adsorption [127], the coordination on Lewis sites of basic but dissociable molecules activates them toward dissociation if a sufficiently basic site is located nearby. This condition can be fulfilled for ionic oxides, thus molecular coordination of water can be precursor for its dissociation, and the overall process is, in principle, reversible (Scheme 9.2). [Pg.268]

Polyphenols Sinapicacid Free and esterified phenolic compounds condensed tannins Dark colour Bitter taste Astringent effects React with fimctional groups at protein, similar to isothiocyanates Use of reducing agents to avoid oxidation Pre-extraction with alcohols Membrane processing Adsorption processing... [Pg.191]

Sometimes, the amount of species adsorbed from a solution onto an adsorbent, e.g. activated carbon, depends on the eiectrical potential applied to the adsorbent the amount adsorbed at equilibrium depends on the potential applied. This equilibrium phenomenon of potential dependent adsorption could provide a basis for potentialswing adsorption. Bisinger and Keiier (1990) have utilized such a phenomenon (see Zabasajja and Savinell (1989) for electrosorption of alcohols on graphite surfaces and references to earlier smdies) to develop a potential-swing adsorption process. They have experimentally studied... [Pg.519]

Within this ehapter we are mostly concerned with physical adsorption. Our first task is to explore some simple and frequently used equations for adsorption isotherms. We will foeus on the acidity/basicity of the adsorbate and adsorbent as a eriterion for the adsorbate-adsorbent interaction energy, and make a special case of the adsorption of aleohol molecules from apolar solvents. The alcohol molecules self-assoeiate and form molecular clusters in apolar and inert solvents. This aggregation proeess may influence the adsorption process and will be encountered when diseussing and analyzing the alcohol adsorption isotherms. [Pg.305]


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See also in sourсe #XX -- [ Pg.31 , Pg.91 ]




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Adsorptive processes

Alcohols adsorption

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