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Miller and Chuang 151(a)3380297329232893235116221456140313050.020.01Time(min.)0.54Absorbance0.410.270.140.0037503438312528132538217518121450Wavenumber (cm -1 )(b)3380297329232893235116221456140313050.02Absorbance0.01Time(min.)0.540.410.140.003750343831252813 2538 2175Wavenumber (cm -1 )18121450Figure 4. (a) Pulsing 1 cm 3 CH 3 CH 2 OH/He (83/17 Vol%) into flowing He/O 2(86/14 Vol% ) at 35 cm 3 /min and 323 K on HAuCl 4 . (b) Pulsing 1 cm 3CH 3 CH 2 OH/He (83/17 Vol%) into flowing He/H 2 O 2 /O 2 (84/2/14 Vol%) at 35cm 3 /min and 323 K on HAuCl 4 .SummaryAu/TiO 2 catalyst prepared from AuCl 3 possesses reduced Au and oxidized Au siteswhich exhibit high CO oxidation activity. The catalyst produce carbonate and
152CO Oxidationcarboxylate species which are potential intermediates during CO and CH 3 CH 2 OHoxidation. Adsorbed oxygen produced from H 2 O 2 promoted both CO andCH 3 CH 2 OH oxidation.AcknowledgementsWe acknowledge partial support from the Ohio Board of Regents for carrying outthis research.References1. M. Haruta, S. Tsubota, T. Kobayashi, H. Kageyama, M. J. Genet, B. Delmon,Journal of Catalysis 144, 175 (1993).2. M. A. P. Dekkers, M. J. Lippits, B. E. Nieuwenhuys, Catalysis Letters 56, 195(1999).3. H. H. Kung, M. C. Kung, C. K. Costello, Journal of Catalysis 216, 425 (2003).4. B. Schumacher, V. Plzak, M. Kinne, R. J. Behm, Catalysis Letters 89, 109(2003).5. S. S. Pansare, A. Sirijaruphan, J. G. Goodwin, Journal of Catalysis 234, 151(2005).6. M. Valden, X. Lai, D. W. Goodman, Science (Washington, D. C.) 281, 1647(1998).7. S. Derrouiche, P. Gravejat, D. Bianchi, Journal of the American ChemicalSociety 126, 13010 (2004).8. J. H. Yang, J. D. Henao, M. C. Raphulu, Y. Wang, T. Caputo, A. J. Groszek, M.C. Kung, M. S. Scurrell, J. T. Miller, H. H. Kung, Journal of Physical ChemistryB 109, 10319 (2005).9. R. T. Tom, A. S. Nair, N. Singh, M. Aslam, C. L. Nagendra, R. Philip, K.Vijayamohanan, T. Pradeep, Langmuir 19, 3439 (2003).10. G. J. Hutchings, M. S. Scurrell, Cattech 7, 90 (2003).11. K. Kunimatsu, A. Aramata, H. Nakajima, H. Kita, Journal of ElectroanalyticalChemistry and Interfacial Electrochemistry 207, 293 (1986).12. S. C. Chang, A. Hamelin, M. J. Weaver, Surface Science 239, L543 (1990).13. M. V. Konduru, S. S. C. Chuang, Journal of Catalysis 187, 436 (1999).14. J. Arana, J. M. Dona-Rodriguez, C. G. i. Cabo, O. Gonzalez-Diaz, J. A. Herrera-Melian, J. Perez-Pena, Applied Catalysis, B: Environmental 53, 221 (2004).15. G. Jacobs, B. H. Davis, Applied Catalysis, A: General 285, 43 (2005).16. S. Tsubota, M. Haruta, T. Kobayashi, A. Ueda, Y. Nakahara, Studies in SurfaceScience and Catalysis 63, 695 (1991).17. K. Ruth, M. Hayes, R. Burch, S. Tsubota, M. Haruta, Applied Catalysis, B:Environmental 24, L133 (2000).18. K. Almusaiteer, S. S. C. Chuang, Journal of Catalysis 180, 161 (1998).
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Catalysis ofOrganic Reactions
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14. Catalyst Manufacture: Laborator
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62. Catalysis of Organic Reactions,
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108. Metal Oxides: Chemistry and Ap
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CRC PressTaylor & Francis Group6000
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xiii14. The Transformation of Light
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xviien Catalisis y Petroquimica (UN
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xix56. Transition Metal Removal fro
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xxiiiChronology of Organic Reaction
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To Zsuzsanna and Tim
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Jones et al. 31. On the Use of Immo
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Jones et al. 5three-phase tests in
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Jones et al. 7In the HKR of rac-epi
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Jones et al. 9term performance char
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Jones et al. 115. A. S. Gruber, D.
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Moses et al. 132. Supported Re Cata
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Moses et al. 15perrhenate, followed
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Moses et al. 17SnCOSnMe 4≡SiOReO
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Moses et al. 19(AlOSi) of the cube.
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Moses et al. 212.510 3 k obs / s -1
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Wang et al. 233. Catalytic Hydrogen
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Wang et al. 25The rate expressions
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Wang et al. 27Schiff’s base forma
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32Halophosphite LigandsIn 1970, Pru
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34Halophosphite LigandsThe ligands,
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36Halophosphite LigandsTable 2 Temp
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38Halophosphite Ligands3. P. W. N.
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40Monolithic Bioreactorstrength for
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42Monolithic BioreactorMenten equat
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Gőbölös et al. 456. Highly Selec
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Gőbölös et al. 47was practically
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Gőbölös et al. 49noteworthy that
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Gőbölös et al. 51Figure 2 NMR sp
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Gőbölös et al. 53internal TMS in
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56Hydrotalcite-like Catalysts[A n-
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58Hydrotalcite-like Catalystssample
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Mantilla, Tzompantzi, Torres and G
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68Synthesis of MIBKwe examined the
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70Synthesis of MIBK1412Conversion (
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72Synthesis of MIBK4,4’-dimethyl
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74Synthesis of MIBKobtained for MIB
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Ardizzi et al. 7710. The Control of
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Ardizzi et al. 79type acidity at th
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Ardizzi et al. 81procedure describe
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84Phenol Benzoylationconsecutive Fr
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86Phenol BenzoylationThis does not
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II. Symposium on Catalytic Oxidatio
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92Oxidation with Microchannel Immob
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Page 127 and 128: 100 Propylene Partial OxidationThe
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Page 137 and 138: 110Oxidation of n-Pentanemethacryli
Page 139 and 140: 112Oxidation of n-PentaneFReqox1ox2
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Page 145 and 146: 118Oxidation of n-PentaneReferences
Page 147 and 148: 120TEMPO Oxidation of Alcoholsthe u
Page 149 and 150: 122TEMPO Oxidation of AlcoholsThe r
Page 151 and 152: 124TEMPO Oxidation of Alcoholsany d
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Page 155 and 156: 128TEMPO Oxidation of AlcoholsMNT :
Page 157 and 158: 130TEMPO Oxidation of Alcoholsuptak
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Page 169 and 170: 142Bromine-Free TEMPO-Based Catalys
Page 175 and 176: 148CO OxidationP25 TiO 2 , respecti
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Page 195 and 196: 168Nitrobenzene Hydrogenationfurthe
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Page 203 and 204: 176Nitrobenzene Hydrogenation10. G.
Page 205 and 206: 178 Hydrogenation of Dehydrolinaloo
Page 215 and 216: 188Modeling Mass Transfer Hydrogena
Page 225 and 226: 198 Fructose HydrogenationHOHCCH 2O
Page 227 and 228: 200 Fructose HydrogenationTable 1.
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202 Fructose Hydrogenationmmol form
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204 Fructose Hydrogenationthe subst
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206 Fructose Hydrogenationcleave th
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208 Fructose Hydrogenationfulfills
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210 Fructose Hydrogenationis not th
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Disselkamp et al. 21324. Cavitating
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Disselkamp et al. 215column. In a p
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Disselkamp et al. 217selectivity es
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Disselkamp et al. 219hydrogenated (
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Disselkamp et al. 221A somewhat mor
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Disselkamp et al. 223Scheme 4.cis-2
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Disselkamp et al. 225conventional c
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Ostgard et al. 22725. The Treatment
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Ostgard et al. 229Table 1. The reac
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Ostgard et al. 231metal atoms. Thes
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Ostgard et al. 233In conclusion, th
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Kuusisto, Mikkola and Salmi 23526.
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Kuusisto, Mikkola and Salmi 237100A
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Kuusisto, Mikkola and Salmi 2399. B
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242 1-Phenyl-1-Propyneof cis-β-met
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244 1-Phenyl-1-Propynealkene. When
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Musolino, Apa, Donato and Pietropao
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Gőbölös and Margitfalvi 25329. R
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Gőbölös and Margitfalvi 255maxim
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Gőbölös and Margitfalvi 257Y=421
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Rothenberg et al. 26130. How to Fin
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Rothenberg et al. 263By dividing th
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Rothenberg et al. 265pre-define the
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Rothenberg et al. 267Table 1. Parti
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Rothenberg et al. 269Experimental S
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Angueira and White 27131. Novel Chl
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Angueira and White 273optimizedgeom
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Angueira and White 275F igure 4 - c
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Angueira and White 277Table 1. 27 A
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Angueira and White 279obtained from
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Robitaille, Clément, Chapuzet and
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Cao, White, Wang and Frye 28933. Se
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Cao, White, Wang and Frye 291Experi
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294Chiral Ferrocene Ligandsnew Twin
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296Chiral Ferrocene LigandsTable 1.
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298Chiral Ferrocene Ligandsprevents
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300Chiral Ferrocene LigandsConclusi
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302Chiral Ferrocene Ligandsextracte
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304 Catalyst Library DesignIn gas p
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306 Catalyst Library Designd−(b 0
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308 Catalyst Library DesignBasic Pr
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310 Catalyst Library DesignD in com
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312 Catalyst Library DesignCatalyst
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314 Catalyst Library Design27. S. H
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316 Dendrimer TemplatesWe are devel
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318 Dendrimer TemplatesThe differen
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320 Dendrimer TemplatesWe encounter
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322 Dendrimer TemplatesThe 100 cm -
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328Rearrangement of 3,4-Epoxy-1-But
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3382,5-Dimethyl-2,4-Hexadieneharves
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348Heteropoly AcidsSOOO O+ +OS1 2 3
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350Heteropoly AcidsTable 3. Acylati
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352Heteropoly AcidsSiO 2 is the bes
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Diez, Di Cosimo and Apesteguia 3554
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Diez, Di Cosimo and Apesteguia 357T
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378 Polyurethane from Natural OilMe
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380 Polyurethane from Natural Oilco
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382 Polyurethane from Natural Oilfr
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384 Polyurethane from Natural OilTh
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386 Carbonylation of Chloropinacolo
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396 Recycling Homogeneous Catalysts
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406“Green” Catalysts for Biodie
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416 Production of BiodieselTable 1.
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418 Production of Biodieselto a mas
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420 Production of BiodieselEthyl st
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422 Production of Biodiesel10080Sel
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424 Production of Biodieselproduct
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Marincean et al. 42747. Glycerol Hy
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Marincean et al. 429Experimental Se
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Marincean et al. 431neutralize all
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Marincean et al. 433suggesting that
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Kocal 43748. Developing Sustainable
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Kocal 439description of the four st
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Kocal 441metallurgy in parts of the
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Kocal 443that capital investment co
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448Propylene Oxidation to POSupercr
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450Propylene Oxidation to POTable 1
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452Propylene Oxidation to PO
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Riermeier et al. 45550. catASium ®
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Riermeier et al. 457It is interesti
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Riermeier et al. 459Reaction of the
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Riermeier et al. 461References1. I.
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464 Chiral 2-Amino-1-Phenylethanolp
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466 Chiral 2-Amino-1-PhenylethanolI
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468 Chiral 2-Amino-1-Phenylethanola
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470 t-Butanol DehydrationResults an
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472 t-Butanol Dehydrationcomprises
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Pohlmann et al 47553. Leaching Resi
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Pohlmann et al 477this study. In th
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Pohlmann et al 479Experimental Sect
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482 Reductive AlkylationSince the p
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484 Reductive AlkylationTable 2. Re
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Wolf, Seebald and Tacke 489100Norma
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Woods et al. 49356. Transition Meta
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Woods et al. 495Effect of oxidation
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502 Electroreductive Catalytic Ullm
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504 Electroreductive Catalytic Ullm
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Catalysis of Organic Reactions 507A
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Catalysis of Organic Reactions 509K
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Catalysis of Organic Reactions 511T
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514 Keyword Indexcarboncarbon dioxi
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516 Keyword Indexethanolamine 16 13
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518 Keyword IndexNi, activated 25 2
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520 Keyword Indexsuccinimido ketone
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