1,721,014 research outputs found
Synthesis Of Mesoporous Silicoaluminophosphates (sapo)
No full textMesoporous silicoaluminophosphates with hexagonal organization were prepared from phosphoric acid, aluminum sulfate, and fumed silica or tetraethylorthosilicate as sources of silicon. Hexadecyltrimethylammonium bromide was the structure directing agent. The material was characterized by X-ray diffraction, pore analysis, 29Si nuclear magnetic resonance with magic angle spinning, elemental analysis and derivative thermogravimetry.141297300Kresge, C.T., Leonowicz, M.E., Roth, W.J., Vartulli, J.C., Beck, J.S., (1992) Nature, 359, p. 710Masson, N.C., Pastore, H.O., (2001) Microporous and Mesoporous Mater., 44-45, p. 173Chakraborty, B., Pulikottil, A.C., Das, S., Viswanathan, B., (1997) Chem. Commun., p. 911Oliveira, E.C., Masson, N.C., Mascarenhas, A.J.S., Pastore, H.O., submittedKimura, T., Sugahara, Y., Kuroda, K., (1999) Chem. Mater., 11, p. 508Caudel, A., Brunel, D., DiRenzo, F., Garrone, E., Fubini, B., (1997) Langmuir, 13, p. 2773De Saldarriaga, L.S., Sadarriaga, C., Davis, M.E., (1987) J. Am. Chem. Soc., 109, p. 268
On The Platinum Species Of Pt/h-mcm-22 Catalyst For Methane Combustion
No full textPt/H-MCM-22 catalysts for methane combustion have been prepared by ion-exchange of a highly crystalline H-MCM-22 zeolite using [Pt(NH3)4](NO3)2. The activation procedure of the catalyst precursor has been optimized and all steps monitored by HRTEM, SEM and FTIR of CO adsorbed. The preliminary decomposition/calcination of the ion exchanged sample is very crucial in that influence the final properties of platinum active species. © 2008 Elsevier B.V. All rights reserved.174B837840Palella, B.I., Albuquerque, A., Cadoni, M., Frache, A., Pastore, H.O., Pirone, R., Russo, G., Marchese, L., (2004) Catal. Comm., 5, p. 191Corma, A., Fornes, V., Guil, J.M., Pergher, S.B., Maesen, Th.L.M., Buglass, J.G., (2000) Microporous Mesoporous Mater., 38, p. 301Jung, H.J., Park, S.S., Shin, C.-H., Park, Y.-K., Hong, S.B., (2007) J. Catal., 245, p. 65Pirngruber, G.D., Seshan, K., Lercher, J.A., (2000) J. Catal., 190, p. 396Kato, S., Nakagawa, K., Ikenaga, N., Sukuki, T., (2001) Catal. Lett., 73, p. 175Taralunga, M., Mijoin, J., Magnoux, P., (2006) Catal. Comm, 7, p. 115Marques, A.L.S., Monteiro, J.L.F., Pastore, H.O., (1999) Microporous Mesoporous Mater., 32, p. 131Albuquerque, A., Marchese, L., Lisi, L., Pastore, H.O., (2006) J. Catal., 241, p. 367Milanesio, M., Croce, G., Frache, A., Mascarenhas, A.J.S., Oliveira, E.C., (2005) Stud. Surf. Sci. Catal., 155, p. 415Chakarova, K., Mihaylov, M., Hadjiivanov, K., (2005) Microporous Mesoporous Mater., 81, p. 305C. Bisio, K. Fajerwerg, J.M. Krafft, P. Massiani, G. Martra, Res. Chem. Intermed., in pres
Meso-alpo Prepared By Thermal Decomposition Of The Organic-inorganic Composite: A Ftir Study
No full textMesporous ALPO was synthesised using cetyltrimethylammonium bromide (CTAB) as a structure-directing agent. FTIR spectroscopy was used to follow the formation of the ALPO mesophase by thermal decomposition of the aluminophosphate/surfactant composite and NH3 was used as probe molecule to monitor the surface acidity of the product.141417422Estermann, M., McCuster, L.B., Baerlocher, C., Merrouche, A., Kessler, H., (1991) Nature, 352, p. 320Davis, M.E., Saldarriaga, C., Montes, C., Garces, J., Crowder, C., (1998) Nature, 331, p. 698Kimura, T., Sugahara, Y., Kuroda, K., (1998) Micropor. Mesopor. Mater., 22, p. 115Masson, N.C., Pastore, H.O., (2001) Micropor. Mesopor. Mater., 44, p. 173Oliveira, E.C., Masson, N.C., Mascarenhas, A.J.S., Pastore, H.O., Colloids and SurfacesPeña, M.L., Dellarocca, V., Rey, F., Corma, A., Coluccia, S., Marchese, L., (2001) Microporous Mesoporous Mat., 44-45, p. 345Marchese, L., Gianotti, E., Maschmeyer, T., Martra, G., Coluccia, S., Thomas, J.M., (1997) Il Nuovo Cimento, 19 D, p. 1707Gianotti, E., Dellarocca, V., Martra, G., Marchese, L., Coluccia, S., Maschmeyer, T., in preparatio
Vanadium-modified Mcm-22 Zeolite
No full textThe synthesis and the characterization of a novel vanadoaluminosilicate, V-MCM-22, with MWW structure, and of vanadyl-exchanged MCM-22 zeolite, [VO]-MCM-22, have been performed. V-MCM-22 was prepared using VOSO4 in the synthesis gel (H+ or Na+-exchanged samples were also prepared), while [VO]-MCM-22 was prepared by ion-exchange of MCM-22 with VO2+ ions. The materials were characterized by X-ray diffraction (XRD) and thermogravimetry (TGA). The presence of redox sites (V 4+/V5+ couples) was monitored by diffuse reflectance (DR) UV-Vis spectroscopy of oxidized (in O2 at 580°C) and reduced (in H2 at 500°C) samples. © 2005 Elsevier B.V. All rights reserved.158 A901908Bellussi, G., Rigutto, M.S., (2001) Stud. Surf. Sci. Catal., 137, p. 911Hartmann, M., Kevan, L., (2002) Res. Chem. Intermed., 28, p. 625Centi, G., Perathoner, S., Trifirò, F., Abukais, A., Aissi, C.F., Guelton, M., (1992) J. Phys. Chem., 96, p. 2617Wark, M., Koch, M., Brückner, A., Grünert, (1998) J. Chem. Soc., Faraday Trans., 94, p. 2033Dzwigaj, S., Matsuoka, M., Anpo, M., Che, M., (2000) J. Phys. Chem. B, 104, p. 6012Prakash, A.M., Kevan, L., (2000) J. Phys. Chem. B, 104, p. 6860Hari Prasad Rao, P.R., Ramaswamy, A.V., Ratnasamy, P., (1992) J. Catal., 137, p. 225Rigutto, M.S., Van Bekkum, H., (1991) Appl. Catal., 68, pp. L1Carl, P.J., Isley, S.L., Larsen, S.C., (2001) J. Phys. Chem. A, 105, p. 4563Rubin, M.K., Chu, P., (1990), U. S. Patent 4 959 325Marques, A.L.S., Monteiro, J.L.F., Pastore, H.O., (1999) Microporous Mesoporous Mater., 32, p. 131Albuquerque, A., Pastore, H.O., Marchese, L., Stud. Surf. Sci. Catal., , in pressSen, T., Rajamohanan, P.R., Ganapathy, S., Sivasanker, S., (1996) J. Catal., 163, p. 354Trujillo, C.A., Uribe, U.N., Knops-Gerrits, P., Oviedo, L.A., Jacobs, P.A., (1997) J. Catal., 168, p.
Cal-4, A Structural Study Of A Dual Templated Chabazite-type Silicoaluminophosphate
No full textCAL-4 is a member of a novel family of SAPOs, which can be prepared from the layered precursor n-butylammonium ALPO-kanemite (nBA ALPO-kan). The usage of a layered starting material was found to have a profound influence on product morphology, acid strength and catalytic site distribution. The crystal structure of the novel chabazite-type material CAL-4 displays a layered organization of the SDAs, which may be responsible for an unusual plate-like particle shape. It is predicted that the morphology of the crystallites can be designed by choosing suitable SDAs. © 2008 Elsevier B.V. All rights reserved.174B917920Cheng, S.F., Tzeng, J.N., (1997) B. Y. Hsu Chem. Mater., 9, p. 1788Martins, G.A.V., Pastore, H.O., (2005) Stud. Surf. Sci. Catal., 158, p. 335H.O. Pastore, G.A.V. Martins, M. Strauss, L.G. Pedroni, G.B. Superti, E.C. de Oliveira, G. Gatti and L. Marchese, Micropor. Mesopor. Mater., in pressWilson, S.T., Flanigen, E.M., (1988) ACS Symp. Ser., 398, p. 329Gieck, C., Bisio, C., Marchese, L., Filinchuk, Y., da Silva, C.E., Pastore, H.O., (2007) Angew. Chem. Int. Ed., 46, p. 889
Spectroscopic And Catalytic Studies On Cu-mcm-22: Effect Of Copper Loading
No full textCopper exchanged MCM-22 zeolites with varying copper contents were prepared, characterized and tested in the nitrous oxide decomposition. Over-exchanged samples showed high activity, comparable to very active Cu-ZSM-5 catalysts. The nature of the copper species was investigated by TPR - H2, FTIR - CO and FTIR - NO, evidencing at least three different species: exchanged Cu2+ ions, cationic oligomeric species and oxidic phases. Upon NO adsorption, mononitrosilic complexes CuI - (NO) were formed, and completely oxidized to CuII - (NO) with increasing NO pressure. Nitrate complexes were extensively formed by reaction with the oxidic phases in the sample with 183% cation exchange level.142 A343350Armor, J.N., (1995) Catal. Today, 26, p. 99Leonowicz, M.E., Lawton, J.A., Lawton, S.L., Rubin, M.K., (1994) Science, 266, p. 1910Corma, A., Palomares, A.E.O., Fornés, V., (1998) Res. Chem. Intermed., 24, p. 613Mascarenhas, A.J.S., Andrade, H.M.C., Pastore, H.O., (2001) Stud. Surf Sci. Catal., 135, p. 322Frache, A., Cadoni, M., Bisio, C., Marchese, L., Mascarenhas, A.J.S., Pastore, H.O., J. Phys. Chem., , SubmittedRobson, H., (1998) Micropor. Mesopor. Mater., 22, p. 551Marques, A.L.S., Monteiro, J.L.F., Pastore, H.O., (1999) Micropor. Mesopor. Mater., 32, p. 131Iwamoto, M., Yahiro, H., Torikai, Y., Yoshoka, T., Mizuno, N., (1990) Chem. Lett., p. 1967Kapteijn, F., Marbán, G., Rodriguez-Mirasol, J., Moulijn, A.J., (1997) J. Catal., 167, p. 271Lamberti, C., Bordiga, S., Salvalaggio, M., Spoto, G., Zecchina, A., Geobaldo, F., Vlaic, M., Belatreccia, M., (1997) J. Phys. Chem. B:, 101, p. 344Márquez-Alvarez, C., McDougall, G.S., Guerrero-Ruiz, A., Rodríguez-Ramos, I., (1994) Appl. Surf Sci., 78, p. 477Wichterlová, B., Dedecek, J., Sobalík, Z., Vondrová, A., Klier, K., (1997) J. Catal., 169, p. 194Borgard, G.D., Molvik, S., Balaraman, P., Root, T.W., Dumesic, J.A., (1995) Langmuir, 11, p. 2065Rakic, V.M., Hercigonja, R.V., Dondur, V.T., (1999) Micropor. Mesopor. Mater., 27, p. 27Wasowicz, T., Prakash, A.M., Kevan, L., (1997) Microporous Mater., 12, p. 107Frache, A., Mascarenhas, A., Cadoni, M., Pastore, H.O., Marchese, L., in preparationJang, H.J., Hall, W.K., D'Itri, J.L., (1996) J. Phys Chem., 100, p. 9416Spoto, G., Bordiga, S., Scarano, D., Zecchina, A., (1992) Catal. Lett., 13, p. 39Palomino, G.T., Bordiga, S., Zecchina, A., Marra, G.L., Lamberti, C., (2000) J. Phys. Chem. B:, 104, p. 8641Konduru, M.V., Chuang, S.S.C., (2000) J. Catal., 196, p. 27
The Surface Acidity Of Mesoporous Silicoaluminophosphates: A Ftir Study
No full textThermally stable mesoporous ALPO and SAPO (Si/Al = 0.6) were synthesised using aluminum sulphate as aluminum source and without the need of HF as mineralizing agent. The mesophases prepared by this procedure were stable to calcination at 773K and presented a structure of non-parallel mesopores in the calcined form. FT-IR spectroscopy supplemented by the use of CO and NH 3 as probe molecules was used to monitor the surface acidity of these new mesoporous materials and indicated that Al-OH, P-OH groups for meso-ALPO and additionally SiOH groups for meso-SAPO are found on the surface of these molecular sieves. The acidities of P-OH and Al-OH are stronger than SiOH in mesoporous silicas but still weaker than the zeolitic Brönsted acid sites.154 B14981504Hartmann, M., Kevan, L., (1999) Chem. Rev., 99, pp. 635-663Sayari, A., Karra, V.R., Reddy, J.S., Moudrakovski, I.L., (1996) Chem. Commun., pp. 411-412Masson, N.C., Pastore, H.O., (2001) Micropor. Mesopor. Mater., 44-45, pp. 173-183Oliveira, E.C., Pastore, H.O., (2002) Stud. Surf. Sci. Catal., 141, pp. 297-300Zhao, D.Y., Luan, Z.H., He, H.Y., Klinowski, J., Kevan, L., (1998) J. Phys. Chem. B, 102, pp. 1250-1259Kimura, T., Sugahara, Y., Kuroda, K., (1998) Chem. Commun., pp. 559-560Chakraborty, B., Pulikottil, A.C., Das, S., Viswanathan, B., (1997) Chem. Commun., pp. 911-912Davis, M.E., Saldarriaga, C., Montes, C., Garves, J., Crowder, C., (1998) Nature, 331, pp. 698-699Estermann, M., McCuster, L.B., Baerlocher, C., Merrouche, A., Kessler, H., (1991) Nature, 352, pp. 320-323Morterra, C., Magnacca, G., (1996) Catal. Today, 27, pp. 497-532Feng, P., Xia, Y., Feng, J., Bu, X., Stucky, G.D., (1997) Chem. Commun., pp. 949-950Gianotti, E., Oliveira, E.G., Dellarocca, V., Coluccia, S., Pastore, H.O., Marchese, L., (2002) Stud. Surf. Sci. Catal., 142, pp. 417-422Marchese, L., Chen, J.S., Wright, P.A., Thomas, J.M., (1993) J. Phys. Chem., 97, pp. 8109-8112Chen, J.S., Wright, P.A., Thomas, J.M., Natarajan, S., Marchese, L., Bradley, S.M., Sankar, G., Lok, C.M., (1994) J. Phys. Chem., 98, pp. 10216-10224Marchese, L., Gianotti, E., Dellarocca, V., Maschmeyer, T., Rey, F., Coluccia, S., Thomas, J.M., (1999) Phys. Chem. Chem. Phys., 1, pp. 585-592Gianotti, E., Dellarocca, V., Oliveira, E.C., Coluccia, S., Pastore, H.O., Marchese, L., (2002) Stud. Surf. Sci. Catal., 142, pp. 1419-1426Gianotti, E., Dellarocca, V., Marchese, L., Martra, G., Coluccia, S., Maschmeyer, T., (2002) Phys. Chem. Chem. Phys., 4, pp. 6109-6115Onida, B., Geobaldo, F., Testa, F., Crea, F., Gamme, E., (1999) Micropor. Mesopor. Mater., 30, p. 119Katovic, A., Giordano, G., Bonelli, B., Onida, B., Garrone, G., Lentz, P., Nagy, J.B., (2001) Micropor. Mesopor. Mater., 44-45, pp. 275-281Onida, B., Borello, L., Bonelli, B., Geobaldo, F., Garrone, E., (2003) J. Catal., 214, pp. 191-199Coluccia, S., Marchese, L., Martra, G., (1999) Micropor. Mesopor. Mater., 30, pp. 43-56Zecchina, A., Lamberti, C., Bordiga, S., (1998) Cat. Today, 41, p. 16
The Synthesis Of Sapo-44 From Lamellar Alpo-kanemite
No full textThis study shows that SAPO-44 molecular sieve may be prepared from AlPO-kanemite as source of phosphorus and aluminum simultaneously, without contamination with other phases. The results showed that the rate of the reaction was dependent on the duration of the ageing time and on dilution. X-rays diffractograms show that the minimum time of hydrothermal treatment necessary to completely transform AlPO-kanemite in SAPO-44 is 36 h. Monitoring of the reaction after different times of hydrothermal treatment shows that no complete dissolution of AlPO-kanemite occurs in the process of SAPO-44 production, thus a local, molecular level rearrangement involving the silica source is proposed for this reaction. © 2005 Elsevier B.V. All rights reserved.158 A335342Wilson, S.T., Flanigen, E.M., (1988) ACS Symp. Ser., 398, p. 329Man, P.P., Briend, M., Peltre, M.J., Lamy, A., Beaunier, P., Barthomeuf, D., (1991) Zeolites, 11, p. 563Prakash, A.M., Unnikrishnan, S., Rao, K.V., (1994) Appl. Catal. A, 110, p. 1International Patent, Exxon Mobil, WO 02/26677 A2Onyestyak, G., Pal-Borbèly, G., Beyer, H.K., (2001) Microporous Mesoporous Mater., 43, p. 73Feng, F., Balkus Jr., J.K., (2004) Microporous Mesoporous Mater., 69, p. 85Cheng, S., Tzeng, J., Hsu, B., (1997) Chem. Mater., 9, p. 1788Albuquerque, A., Coluccia, S., Marchese, L., Pastore, H.O., (2004) Stud. Surf. Sci. Catal., 154 A, p. 966Akolekar, D.B., Bhargava, S.K., Gorman, J., Paterson, P., (1999) Colloids and Surfaces A: Physicochem. Eng. Aspects, 146, p. 375Marchese, L., Chen, J., Wright, P.A., Thomas, J.M., (1993) J. Phys. Chem., 97, p. 8109Ashtekar, S., Chilukuri, S.V.V., Chakrabarty, D.K., (1994) J. Phys. Chem., 98, p. 487
Thermal Decomposition Of (η6-benzene)tricarbonylchromium(0) Inside The α-cages Of The Na56 Y Zeolite
Full text linkWe present here the first results that show the different thermal stabilities of the complex (η6-benzene)tricarbonylchromium(0), [Cr(η6-C6H6)(CO)3], when anchored at different sites inside the a-cages of zeolite Na56 Y, sites 1 and 2. When the system is heated under dynamic vacuum, the complex anchored at site 1, in which the interactions C6H6-Na + and Na+-OC are stronger, decomposes slower than the complex anchored at site 2, in which such interactions are weaker. When the system is heated under static vacuum, the rates of decomposition of the complex anchored in both sites are comparable. The complex inside Na56 Y is less stable than the same complex in the solid state.15179Gates, B.C., Guczi, L., Knozinger, H., (1986) Metal Clusters in Catalysis, , Elsevier: AmsterdamOzin, G.A., Gil, C., (1989) Chem. Rev., 89, p. 1749Ozin, G.A., Kuperman, A., Stein, A., (1989) Angew. Chem. Int. Ed., 28, p. 359Stucky, G.D., Macdougall, J.E., (1990) Science, 247, p. 433Zecchina, A., Otero-Arean, C., (1993) Catal. Rev.-Sci. Eng., 35, p. 261Bein, T., (1996) Comprehensive Supramolecular Chemistry, 7. , Lehn, J.-M.Atwood, J.L.Davies, J.E.D.MacNicol, D.D.Vögtle, F., eds.Pergamon: Oxford, ch. 20Psaro, R., Recchia, S., (1998) Catal. Today, 41, p. 139Brémard, C., (1998) Coord. Chem. Rev., 180, p. 1647Shen, G.C., Liu, A.M., Ichikawa, M.J., (1998) J. Chem. Soc., Faraday Trans., 94, p. 1353Muller, B.R., Calzaferri, G., (1998) Microporous Mesoporous Mater., 21, p. 59Özkar, S., Ozin, G.A., Moller, K., Bein, T., (1990) J. Am. Chem. Soc., 112, p. 9575Ozin, G.H., Özkar, S., Pastore, H.O., Pöe, A.J., Vichi, E.J.S., (1992) ACS Symp. Series, 499, p. 314Brémard, C., Ginestet, G., Le Maire, M., (1996) J. Am. Chem. Soc., 118, p. 12724Shirley, W., Scoville, S.P., (2000) Microporous Mesoporous Mater., 37, p. 271Huang, Y., Poissant, R.R., (2002) Langmuir, 18, p. 5487Pastore, H.O., Ozin, G.A., Pöe, A.J., (1993) J. Am. Chem. Soc., 115, p. 121
Performance Of Pd Supported On Mesoporous Molecular Sieves On Methane Combustion
No full textThe performance of Pd-based catalysts supported on mesoporous molecular sieves with different pore arrangement (MCM-41 and MCM-48) was investigated for methane combustion. All molecular sieves showed to be thermally stable, evidencing the suitability of these materials as support for high temperature processes and motivated the efforts to exploit their use. Reaction data showed that silicate-based samples rendered more active catalysts than those prepared on aluminosilicate; activity was affected by monodimensional or three-dimensional pore arrangement. The use of molecular sieves in proton form led to an increase in the reaction rate in relation to the sodium form. © 2011 Elsevier B.V. All rights reserved.2516Gélin, P., Primet, M., (2002) Applied Catalysis B: Environmental, 39, pp. 1-37Wierzchowski, P.T., Zatorski, L.W., (2003) Applied Catalysis B: Environmental, 44, pp. 53-65Choudhary, T.V., Banerjee, S., Choudhary, V.R., (2005) Catalysis Communications, 6, pp. 97-100Yuranov, I., Moeckli, P., Suvorova, E., Buffat, P., Kiwi-Minsker, L., Renken, A., (2003) Journal of Molecular Catalysis A, 192, pp. 239-251Maeda, H., Kinoshita, Y., Reddy, K.R., Muto, K., Komai, S., Katada, N., Niwa, M., (1997) Applied Catalysis A, 163, pp. 59-69Wierzchowski, P.T., Zatorski, L.W., (2002) Catalysis Letters, 78, pp. 171-176Okumura, K., Matsumoto, S., Nishiaki, N., Niwa, M., (2003) Applied Catalysis B: Environmental, 40, pp. 151-159Ishihara, T., Sumi, H., Takita, Y., (1994) Chemistry Letters, 23, pp. 1499-1502Takita, Y., Ishihara, T., Nishiguchi, H., Sumi, H., (1997) Studies in Surface Science and Catalysis, 105, pp. 1647-1654Venezia, A.M., Murania, R., Pantaleo, G., Deganello, G., (2007) Journal of Catalysis, 192, pp. 94-102Ruiz, J.A.C., Fraga, M.A., Pastore, H.O., (2007) Applied Catalysis B: Environmental, 76, pp. 115-122Wang, Z.J., Liu, Y., Shi, P., Liu, C.J., Liu, Y., (2009) Applied Catalysis B: Environmental, 90, pp. 570-577Bassil, J., Albarazi, A., Da Costa, P., Boutros, M., (2011) Catalysis Today, 176, pp. 36-40Pastore, H.O., Munsignatti, M., Bittencourt, D.R.S., Rippel, M.M., (1999) Microporous and Mesoporous Materials, 32, pp. 211-228Cónsul, J.M.D., Peralta, C.A., Benvenutti, E.V., Ruiz, J.A.C., Pastore, H.O., Baibich, I.M., (2006) Journal of Molecular Catalysis A, 246, pp. 33-38Xia, Y., Mokaya, R., (2003) Journal of Materials Chemistry, 13, pp. 657-659Panpranot, J., Pattamakomsan, K., Goodwin, J.G., Praserthdam, P., (2004) Catalysis Communications, 5, pp. 583-590Araujo, A.S., Fernandes, Jr.V.J., Veríssimo, S.A., (2000) Journal of Thermal Analysis and Calorimetry, 59, pp. 649-655Bezman, R., (1981) Journal of Catalysis, 68, pp. 242-244Fraga, M.A., Souza, E.S., Villain, F., Appel, L.G., (2004) Applied Catalysis A, 259, pp. 57-63Pena, M.L., Kan, Q., Corma, A., Rey, F., (2001) Microporous and Mesoporous Materials, 44, pp. 9-16Rakai, A., Tessier, D., Bozon-Verduraz, F., (1992) New Journal of Chemistry, 16, pp. 869-875Lomot, D., Juszczyk, W., Pielaszek, J., Kaszkur, Z., Bakuleva, T.N., Karpinski, Z., (1995) New Journal of Chemistry, 19, pp. 263-273Ruiz, J.A.C., Melo, D.M.A., Souza, J.R., Alcazar, L.O., (2002) Materials Research, 5, pp. 173-178Sekizawa, K., Widjaja, H., Maeda, S., Ozawa, Y., Eguchi, K., (2000) Applied Catalysis A, 200, pp. 211-217Eguchi, K., Arai, H., (2001) Applied Catalysis A, 222, pp. 359-367M'Ramadj, O., Li, D., Wang, X., Zhang, B., Lu, G., (2007) Catalysis Communications, 8, pp. 880-884Truitt, M.J., Toporek, S.S., Rovira-Hernandez, R., Hatcher, K., White, J.L., (2004) Journal of the American Chemical Society, 126, pp. 11144-11145Wang, J.G., Liu, C.J., (2006) Journal of Molecular Catalysis A, 247, pp. 199-205Liu, W., Flytzani-Stephanopoulos, M., (1995) Journal of Catalysis, 153, pp. 304-316Zhang, C.J., Hu, P., (2002) The Journal of Chemical Physics, 116, pp. 4281-4285Fujimoto, K., Ribeiro, F., Avalos-Borja, M., Iglesia, E., (1998) Journal of Catalysis, 179, pp. 431-44
- …
