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Abstrakty
The method of utilization of alcohol fraction containing mainly primary alcohols is proposed. The fraction is a waste product arising in the process of cyclohexanone manufacturing. Alcohols are converted into symmetrical and asymmetrical ketones. The reaction proceeds in a continuous manner in the gas phase at the temperature range of 330 - 450°C in a flow reactor with fixed bed containing Zr-Mg-Y-0 catalyst. After processing the initial fraction at the temperature of 420°C and with the load of lh exp -1, a ketone fraction containing mainly nonanone-5 (over 40%, which corresponds to 75% yield and 80% selectivity) was produced. Apart from nonanone-5 in the fraction were such ketones as heptanone-4, octanone-4, cyclohexanone and other; the total content of ketones in the obtained fraction was 58%.
Czasopismo
Rocznik
Tom
Strony
10--12
Opis fizyczny
Bibliogr. 18 poz., wykr.
Twórcy
autor
- Institute of Low Temperature and Structure Research PAS, ul. Okólna 2, 50-422 Wrocław, Poland
autor
- Institute of Inorganic Technology and Mineral Fertilizers, Technical University of Wrocław, Poland
autor
- Institute of Low Temperature and Structure Research PAS, ul. Okólna 2, 50-422 Wrocław, Poland
autor
- Institute of Microsystem Technology, Technical University of Wrocław, Poland
autor
- Institute of Organic Chemistry, Biochemistry and Biotechnology, Technical University of Wrocław, Poland
autor
- Institute of Organic Chemistry and Technology, Technical University of Kraków, Poland
Bibliografia
- (1) Krzysztoforski, A., Łonak, B., Cyclopol - New Export Speciality, Przem. Chem., 1987, 66, 326.
- (2) Wais, J., Izydorczyk, K., Polish Process of Caprolactam, Przem. Chem., 1987, 66, 338.
- (3) Bisok, M., Utilization of alcohols fraction arising in the process of cyclohexane oxidation to cyclohexanone, Master's Thesis, Institute of Organic Chemistry and Technology, Technical University of Kraków, 1999.
- (4) Loginov, G. A., Markov, M. A., Minachev, Kh.M., Studies of the mechanim of alcohols ketonization over oxides of rare earth elements), Neftekhimiya, 1970, 10, 393.
- (5) Takeshita, K., Nakamura, S., Kawamoto, K., Reduced Copper Catalyzed Conversion of Primary Alcohols into Esters and Ketones, Bull. Chem. Soc. Jpn., 1978, 51, 2622.
- (6) Hattori, H., Heterogeneous Basic Catalysis, Chem. Rev., 1995, 95, 537.
- (7) Wrzyszcz, J., Grabowska, H,, Klimkiewicz, R., Syper, L., Reactions of nomal alcohols in the presence of a dehydrogenating iron catalyst, Catal. Lett., 1998, 54, 55.
- (8) Wrzyszcz, J., Grabowska, H., Klimkiewicz, R., Syper, L., Catalytic reactions of oxidized n-C10, derivatives over an iron oxide, Appl. Catal. A: General, 1999, 185, 153.
- (9) Solomons, T. W. G., Fundamentals of Organic Chemistry, J.Wiley & Sons, New York, 1982, 553.
- (10) March, J., Advanced Organic Chemistry, Wiley, lV th ed., New York, 1992.
- (11) Teterycz H., Licznerski B. W., Klimkiewicz R., Wiśniewski K., Nitsch, K., Zgł. Pat. P 338306, 2000.
- (12) Zirconium in Catalysis, Moles P. J. (Editor), in Catal. Today, 1994, 20/2.
- (13) Ross, J. G. H., Xue, E., O'Keeffe, M., A study of Pt/ZrO2 catalysts for water-gas shift reaction in the presence of H2S, Proceedings of the 12th ICC, Studies in Surface Science and Catalysis, 2000, 130, 3813.
- (14) Teterycz, H., Licznerski, B. W., Klimkiewicz, R., Wiśniewski, K., Nitsch, K., Zgł. Pat. P 338307, 2000.
- (15) 2nd Congress of Chemical Technology, Resolution, Wrocław, 15 Sept. 1997.
- (16) Taniewski, M., Prioritary domains in the field of chemical technology in Poland, Przem. Chem., 1997, 76, 515.
- (17) Zieliński, S., Chemical technology tasks according to ecodevclopment and coefficient "10" requirements. Chemik, 1997, 50, 287.
- (18) Arntz. D., Trends in the industry, Catal. Today. 1993, 18, 173.
Typ dokumentu
Bibliografia
Identyfikator YADDA
bwmeta1.element.baztech-article-BUS3-0020-0052