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Effect of Acid Activation on the De-Tert-Butylation Activity of Some Jordanian Clays

Published online by Cambridge University Press:  28 February 2024

Sabri Mahmoud
Affiliation:
Chemistry Department, Yarmouk University, Irbid, Jordan
Sadiq Saleh
Affiliation:
Chemistry Department, Yarmouk University, Irbid, Jordan
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Abstract

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Jordanian natural kaolin and bentonite show good catalytic activity towards debutylating 2-tert-butylphenol, and varying debutylation vs. isomerization selectivity after acid activation. The resulting catalytic activity of these samples is dependent on the acid employed for activation; the samples treated with acetic acid showed relatively low conversions, whereas those treated with hydrochloric or phosphoric acid were found to be very active. Treatments with strong acids such as HCl have various effects on the activity of the samples depending on the concentration of the acid. For example, treatment with 1 M HCl gives the highest activity, whereas a treatment using 12 M HCl produced the lowest activity. The debutylation selectivity of the acid-activated samples is affected by the acid type and/or concentration. This selectivity ranges from 20 to 60%, whereas that of water-treated samples is between 46–82%.

Type
Research Article
Copyright
Copyright © 1999, The Clay Minerals Society

References

Al-No’aimei, M.Z., 1997 The effect of acid and thermal pre-treatment on the catalytic activity of Jordanian bentonite Irbid, Jordan Yarmouk Univ..Google Scholar
Auer, H. and Hofmann, H., 1993 Pillared clays: Characterization of acidity and catalytic properties and comparison with some zeolites Applied Catalysis A; General 97 2338 10.1016/0926-860X(93)80064-W.CrossRefGoogle Scholar
Benesi, H.A., 1956 Acidity of catalyst surfaces I: Acid strength from colors of adsorbed indicators Journal of the American Chemical Society 78 54905494 10.1021/ja01602a008.CrossRefGoogle Scholar
Chitnis, S.R. and Sharma, M., 1997 Industrial application of acid-treated clays as catalysts Reactive and Functional Polymers 32 93115 10.1016/S1381-5148(96)00074-0.CrossRefGoogle Scholar
Clark, J.H. Macquarrie, D.J. and Duncan, J., 1997 Heterogeneous catalysis in liquid phase transformations of importance in the industrial preparations of fine chemicals Organic Process Research and Development 1 149162 10.1021/op960008m.CrossRefGoogle Scholar
Corma, A. and Wojciechowski, B.W., 1985 The chemistry of catalytic cracking Catalysis Reviews: Science and Engineering 27 29150 10.1080/01614948509342358.CrossRefGoogle Scholar
Gill, R. Petkovic, L.M. and Larsen, G., 1998 Interaction of isobutene with the surface of different solid acids Journal of Catalysis 179 5663 10.1006/jcat.1998.2192.CrossRefGoogle Scholar
Gao, Z. and Jiao, J., 1989 Catalytic performance of pillared interlayered clay molecular sieves with high thermal stability Wuli Hauxue Xuebao 5 178184.Google Scholar
Gonzalez, F. Pessquera, C. Benito, I. and Mendio, O.Z., 1992 Synthesis and characterization of Al-Ga pillared clays with high thermal and hydrothermal stability Inorganic Chemistry 31 727731 10.1021/ic00031a007.CrossRefGoogle Scholar
Greensfelder, B.S. Voge, H.H. and Good, G.M., 1949 Catalytic cracking of pure hydrocarbons Industrial and Engineering Chemistry 38 10331040.Google Scholar
Johne, R. and Severin, D., 1965 Die oberflachenmessung mit dem areameter Chemie-Ingenieur-Technik 37 5761 10.1002/cite.330370112.CrossRefGoogle Scholar
Komadel, P. Janek, M. Madejova, J. Weeks, A. and Breen, C., 1997 Acidity and catalytic activity of mildly acid-treated Mg-rich montmorillonite and hectorite Journal of The Chemical Society Faraday Transactions 93 42074210 10.1039/a705227h.CrossRefGoogle Scholar
Li, T.S. and Jin, T.S., 1996 Organic reactions catalyzed by montmorillonite clays Youji Huaxue 16 385402.Google Scholar
Lucio, F., 1973 Comparison of the methods for the determination of surface acidity of solid catalysts Catalysis Reviews: Science and Engineering 8 65115.Google Scholar
Lussier, R.J., 1991 A novel clay-based catalytic material: Preparation and properties Journal of Catalysis 129 225237 10.1016/0021-9517(91)90026-Z.CrossRefGoogle Scholar
Mokaya, R. and Jones, W., 1995 Pillared clays and pillared acid-activated clays: A comparative study of physical, acidic and catalytic properties Journal of Catalysis 153 7685 10.1006/jcat.1995.1109.CrossRefGoogle Scholar
Newman, A.C.D. Brown, G. and Newman, A.C.D., 1987 The chemical constitution of clays Chemistry of Clays and Clay Minerals Alabama Longman, Birmingham 237274.Google Scholar
Ravichandran, J. Lakshmanan, C.M. and Sivasankar, B.N., 1996 Acid-activated montmorillonite and vermeculite clays as dehydration and cracking catalysts Reaction Kinetics and Catalysis Letters 59 301308 10.1007/BF02068127.CrossRefGoogle Scholar
Rupert, J.R. Granquist, W.T. Pinnavaia, T.J. and Newman, A.C.D., 1987 Catalytic properties of clay minerals Chemistry of Clays and Clay Minerals 275318.Google Scholar
Saleh, S.A. and Mahmoud, S.S., 1998 Catalytic debutylation of tert-butylphenols by some natural clays Reaction Kinetics and Catalysis Letters 64 373380 10.1007/BF02475359.CrossRefGoogle Scholar
Shertukde, P.V. Hall, W.K. Dereppe, J.M. and Marcelin, G., 1993 Acidity of H-Y Zeolites: Role of extralattice aluminum Journal of Catalysis 139 468481 10.1006/jcat.1993.1041.CrossRefGoogle Scholar
Tanabe, K. and Anderson, J.R., 1983 Solid acid and base catalysts Catalysis: Science and Technology Berlin Academie-Verlag 231273.Google Scholar
Tkac, I. Komadel, P. and Muller, D., 1994 Acid-treated montmorillonites: A study by Si-29 and Al-27 MAS NMR Clay Minerals 29 1119 10.1180/claymin.1994.029.1.02.CrossRefGoogle Scholar
Upadhya, T.T. Daniel, T. Sudalai, A. Ravindraanthan, T. and Sabu, K.R., 1996 Natural kaolinitic clay: A mild and efficient catalyst for the tetrahydropyranylation and trimethylsilylation of alcohols Synthetic Communications 26 45394544 10.1080/00397919608004777.CrossRefGoogle Scholar