Selective Oxidation and Oxidative Dehydrogenation of Isobutane on Mo-V-Te-P Mixed Metal Oxide Catalysts

• Autorzy: Guan J. , Wang G. , Jing S. , Wang Z. , Kan Q.
• Języki publikacji: EN

Abstrakty

EN

MoV0.3Te0.23Px (x = 0-0.5) catalysts have been prepared and tested in the selective oxidation of isobutane. Among them, MoV0.3Te0.23P0.3 catalyses the direct oxidation of isobutane to methacrolein and methacrylic acid with 33% selectivity, and a total dehydrogenation (olefin plus methacrolein andmethacrylic acid) selectivity up to 63%at 400 graduate C.

Słowa kluczowe

EN

isobutane; isobutylene; selective oxidation; mixed metal oxides catalysts

• Wydawca: Polskie Towarzystwo Chemiczne
• Czasopismo: Polish Journal of Chemistry
• Rocznik: 2006
• Tom: Vol. 80, nr 8
• Strony: 1397--1405
• Opis fizyczny: Bibliogr. 35 poz., rys.

Twórcy

autor

Guan J.

autor

Wang G.

autor

Jing S.

autor

Wang Z.

autor

Kan Q.

• College of Chemistry, Jilin University, JieFang Road 2519, Changchun, 130023, China

Bibliografia

• 1.Nilsson R., Lindblad T. and Andersson A., J. Catal., 148, 501 (1994).
• 2.Inowe T., Asakwra K. and Iwasawa Y., J. Catal., 171, 184 (1998).
• 3.Cavani F. and Trifiro R, Catal.Today, 51, 561 (1999).
• 4.Kung H.H., Adv. Catal., 40, l (1994).
• 5.Moffat J.B., Appl Catal., 146, 34 (1996).
• 6.Schindler G., Ui T. and Nagai K., Appl Catal.. A: Gen., 206, 183 (2001).
• 7.Yoshihiko N., Motomasa O., Koichi N. and Hiroshi S., Eur. Pat. 0418657 A2 (1990).
• 8.Mizuno N. and Misono M., Chem. Rev., 98, 199 (1998).
• 9.Setsuo Y. and Tatsuo Y., US Pat. 5,191,116 (1993).
• 10.uichi K. and Hideo O., US Pat. 6476259 B2 (2001).
• 11.Inumaru K., Ono A., Kubo H. And Misono M., J. Chem. Soc. Faraday Trans., 94, 1765 (1998).
• 12.Kozhevnikov I.V., Catal.. Rev.-Sci. Eng., 37,311 (1995).
• 13.Langpape M., Millet J.M., Ozkan U.S. And Delichere P., J. Catal., 182, 148 (1999).
• 14.Izumi Y., Urabe K. and Onaka A., in: Zeolite, Clay, and Heteropolyacids in Organic Reactions, ' Kodansha/VCH, Tokyo/Weinheim, 1992.
• 15.Yamamatsu S. and Yamaguchi T., Jap. Pat. 02-042032 (1990).
• 16.Cavani F. and Trifiro F., Appl. Catal.. A: Gen., 88, 115 (1992).
• 17.Shishido T., Inoue A., Konishi T,, Matsuura I. and Takehira K., Catal.Lett., 68, 215 (2000).
• 18.Bart J.C.J., Cariati F. and Sgamelloti A., Inorg. Chim. Acta, 36, 105 (1979).
• 19.Paul J.S., Jacobs P.A., Weiss P-A.W. and Maier W.F., Appl. Catal. A: Gen., 265, 185 (2004).
• 20.Paul J.S., GroothaertM.H., KirschhockC.E.A., LebedevO.L., Jacobs P.A. and Maier W.F., Catal. Today,91-92, 265 (2004).
• 21.Paul J.S., Urschey J., Jacobs P.A., Maier W.F. and Verpoort F., J. Catal.., 220, 136 (2003).
• 22.Al-Saeedi J.N., Vasudevan V.K. and Guliants V.V., Catal. Commun., 4, 537 (2003).
• 23.Botella P., López Nieto J.M., Solsona B., Mifsud A. and Marquez F., J. Catal.., 209,445 (2002).
• 24.Jiang H.C., Lu W.M. and Wan H.L., J. Mol Catal. A: Chem., 208, 213 (2004).
• 25.Botella, P., López Nieto J.M. and Solsona B., Catal. Lett., 78, 383 (2002).
• 26.Botella P., Concepción P., López Nieto J.M. and Solsona B., Catal.Lett., 89, 249 (2003).
• 27.Ueda W. and Oshihara K., Appl. Catal.. A: Gen., 200, 135 (2000).
• 28.Cavani F., Mezzogori R. and Trovarelli A., J. Mol. Catal. A: Chem., 204-205, 599 (2003).
• 29.KnappC.,UiT.,Nagai K. and Mizuno N., Catal.. Today,71, 111 (2001).
• 30.Bosch H. and Sinot P.J., J. Chem. Soc., Faraday Trans, l, 85, 1425 (1989).
• 31.Parmaliana A., Arena F. and Frusteri F., Stud. Sturf. Sci. Catal., 110,347 (1997).
• 32.Adamski A., Sojka Z. and Dyrek K., Langmuir, 15, 5733 (1999).
• 33.Botto I.L., Cabello C.I. and Thomas H.J., Mater. Chem. Phys., 47, 37 (1997).
• 34.Chen L.Q., Liang J., Lin H., Weng W.Z., Wan H.L. and Vedrine J.C., Appl. Catal. A: Gen., 293,
• 35.Cutrufello M.G., De Rossi S., Ferino I., Monaci R., Rombi E. And Solinas V., Thermochim. Acta, 434,62 (2005).