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  • Chemistry  (6)
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  • 1
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    AIChE Journal 26 (1980), S. 862-865 
    ISSN: 0001-1541
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: The use of a single compound as the agent in modifying the apparent relative volatility in extractive distillation is well known. In the separation of ethylbenzene from para- and meta-xylenes by extractive distillation, it was found that mixtures containing from two to four components were more effective than any known single compound. Hundreds of combinations of extractive agents were investigated in vapor-liquid equilibrium stills, and from these, twenty-seven different combinations of chlorinated organic compounds showed merit. The relative volatility of ethylbenzene to p-xylene is 1.06 and to m-xylene 1.08. The promising combinations were investigated in three glass perforated plate extractive distillation columns containing twelve, fifteen and nineteen theoretical plates, respectively. Of the twenty-seven different extractive agents tested in the columns, sixteen yielded a relative volatility greater than 1.20. The best one, a mixture of pentachlorophenol, benzene hexachloride and 1,2,4-trichlorobenzene, gave a relative volatility of 1.27. Other combinations approaching this relative volatility are pentachlorophenol, benzene hexachloride and 2,4-dichlorotoluene giving 1.25 and polychlorobenzene, pentachlorophenol, benzene hexachloride and 1,2,4-trichlorobenzene giving 1.26, when used in the ratio of two parts of extractive agent to one part of ethylbenzene-xylene mixture. All the extractive agents boil sufficiently above xylene to make their recovery by distillation easy and complete. Life studies showed no excessive decomposition of any of them while in use.
    Additional Material: 2 Tab.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    AIChE Journal 29 (1983), S. 694-696 
    ISSN: 0001-1541
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Additional Material: 1 Tab.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    AIChE Journal 29 (1983), S. 961-966 
    ISSN: 0001-1541
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: Benzene and toluene are virtually impossible to separate from close boiling nonaromatic hydrocarbons by rectification. Benzene and toluene can be readily separated from similar boiling nonaromatics by using extractive distillation in which the extractive distillation agent is a proper mixture of organic compounds boiling higher than benzene or toluene. A typical extractive distillation agent for benzene is a mixture of phthalic anhydride, maleic anhydride, and adiponitrile; for toluene, phthalic anhydride, maleic anhydride, and glycerol triacetate.
    Additional Material: 5 Tab.
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  • 4
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    AIChE Journal 30 (1984), S. 871-874 
    ISSN: 0001-1541
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Additional Material: 4 Tab.
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  • 5
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    AIChE Journal 31 (1985), S. 504-506 
    ISSN: 0001-1541
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: Extractive distillation can not only negate azeotropes to produce pure compounds by rectification but in some cases will reverse the volatility and bring out the less volatile component before the more volatile component. As an example, isopropyl ether, b.p. = 68.5°C, was distilled off as the overhead from mixtures with acetone, b.p. = 56.2°C, leaving the acetone in the stillpot and column until all the isopropyl ether was removed. This reversal phenomenon does not occur in the isopropyl ether-methyl ethyl ketone system, although the azeotrope is negated.
    Additional Material: 2 Ill.
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  • 6
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    AIChE Journal 30 (1984), S. 845-849 
    ISSN: 0001-1541
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Additional Material: 3 Tab.
    Type of Medium: Electronic Resource
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