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Methane separating mixtures with

Repeat step 8 with the remaining methanol solution. Dissolve any sticky, brown solid left in the round-bottomed flask in 200 mL of dichloro-methane, and add this solution to the aqueous mixture. Shake the phases together and separate. Extract the aqueous mixture with dichloromethane (3 x 200 mL). [Pg.126]

The permselectivity of hydrocarbon vapors, p, is dominated by the sorption component, and sorption of hydrocarbon vapors by rubbery polymers is determined by the condensability of their vapors. It can be seen from Table 9.3, that in organosilicon polymers the propane/methane sorption selectivity, is 10.5-16.2, whereas diffusion selectivity, is only 0.16-0.41. Refs. [39 3] report values of permselectivity of hydrocarbon mixtures with nitrogen for organosilicon membranes produced by GKSS (see Figure 9.10). It can be seen that separation selectivity increases with rising boiling temperature of the hydrocarbon, which points to domination of the sorption component of selectivity. [Pg.243]

Berger, T.A. Deye, J.F. Separation of benzene poly-carhoxylic acids hy packed column supercritical fluid chromatography using methane-carhon dioxide mixtures with very polar additives. J. Chromatogr. Sci. 1991, 29, 141-146. [Pg.689]

Helium is an unreactive noble gas often found in underground deposits mixed with methane. The mixture is separated by cooling the gaseous mixture until all but the helium has liquified. [Pg.318]

As is the case with methane, experiments have been performed with ethane for the purpose of separation of gaseous mixtures in analytical procedures. Phillips37 found that ethane was oxidized in a 3.1 per cent mixture with air at 450° C. over palladium asbestos. Mixtures of ethane and methane are difficult to separate by preferential combustion over platinum or palladium but hydrogen may be removed from such mixtures due to its lower reaction temperature.31 The nature of the products obtained from the hydrocarbon oxidation in these experiments was not reported. [Pg.195]

The mixture is cooled to room temperature, the flask is filled two-thirds full with water, and stirring is continued for five minutes. The xylene solution is separated, washed with water, dried over calcium chloride, filtered, and distilled under reduced pressure. After removal of the solvent, the tricarbomethoxy-methane distils at 128-142 °f 18 mm. The yield of crude product is 50-51 g. (47-48 per cent of the theoretical amount). This material becomes semi-solid on cooling. [Pg.100]

The thermal chlorination of methane is carried out on a large scale in this country by Dow Chemical Company, Diamond Alkali Company, and Allied Chemical Dye Corporation, Solvay Process Division. High-purity methane is mixed with cycle gas and then with chlorine and the mixture introduced into a packed reactor heated to 350-400 C, where chlorine is completely reacted in the excess of hydrocarbon and chlorinated hydrocarbon. The effluent gases contain excess methane and all the chlorinated methanes, which may be separated after condensation by fractional distillation. When reaction temperatures are increased, a competing reaction develops with the formation of perchloroethylene. [Pg.228]

Atoms-to-Mass Conversion Helium (He) is an unreactive noble gas often found in underground deposits mixed with methane. The mixture is separated by cooling the gaseous mixture until all but the helium has liquefied. A party balloon contains 5.50 X 10 atoms of helium gas. What is the mass, in grams, of the helium ... [Pg.331]

Zeolite membranes show high thermal stability and chemical resistance compared with those of polymeric membranes. They are able to separate mixtures continuously on the basis of differences in the molecular size and shape [18], and/or on the basis of different adsorption properties [19], since their separation ability depends on the interplay of the mixture adsorption equilibrium and the mixture. Different types of zeolites have been studied (e.g. MFI, LTA, MOR, FAU) for the membrane separation. They are used still at laboratory level, also as catalytic membranes in membrane reactors (e.g. CO clean-up, water gas shift, methane reforming, etc.) [20,21]. The first commercial application is that of LTA zeolite membranes for solvent dehydration by pervaporation [22], Some other pervaporation plants have been installed since 2001, but no industrial applications use zeolite membranes in the GS field [23]. The reason for this limited application in industry might be due to economical feasibility (development of higher flux membranes should reduce both costs of membranes and modules) and poor reproducibility. [Pg.284]

An example of the separation of a methane-iso-butane-n-butane mixture with splitless injection of 0.5 ml of the sample into a glass capillary column with a silica layer is given in paper [26]. The analysis time is less than 1 min. Incidentally, splitless injection of a sample was already used in an earlier period of adsorption capillary column development (see, for example, Fig. 3-4 [70]). [Pg.78]

Dynamic studies of the adsorption of methane, benzene and cyanogen chloride were stimulated in the fixed bed batch processes for several adsorbents to be used in various purification and separation techniques. The investigation of low temperature nitrogen adsorption from its mixtures with helium was carried out... [Pg.511]


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