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Mantilla, Tzompantzi, Torres and Gómez 65References1. R. J. Quann, L.A. Green, S.A. Tabak and F.J. Krambeck. Ind. Eng. Chem. Res.,27, 565-570 (1988).2. J.F. Izquierdo, M.Vila, J.Tejero, F.Cunill and M.Iborra. Appl.Catal. A: General,106, 155-165 (1993).3. A.P.Vogel, A.T. O´Connor and M.Kojima. Clay Minerals, 25, 355-362 (1990).4. A. Reffinger and U. H<strong>of</strong>fman, Chem. Eng. Technol; 13, 150 (1990).5. G. Busca, G. Ramis and V. Lorenzelli; J.Chem. Soc. Trans., 85(1), 137-146(1998).6. A. Saus and E. Schmidt; J. Catal., 94, 187-194 (1998).7. B. Nkosi, F.T.T. Ng and G.L. Rempel; Appl.Catal.A: General, 158, 225-241(1997).8. B. Nkosi, F.T.T. Ng and G.L. Rempel; ApplCatal. A: General, 161, 153-166(1997).9. J. Heveling, C.P. Nicolaides and M.S. Scurrell; ApplCatal.A: General, 248, 239-248 (2003).10. W. Zhang, Ch. Li, R. He, X. Han and X. Bao. Catal.Letters, 64, 147-150 (2000).11. A.S. Chellapa, R.C. Millar and W.J.Thompson; Appl.Catal. A: General, 209,359-374 (2001).12. A. Mantilla, G. Ferrat, A. López-Ortega, E. Romero, F. Tzompantzi, M. Torres,E. Ortíz-Islas and R. Gómez; J. Mol. Cat. A: Chemical, 228, 333-338 (2005).13. A. Mantilla, G. Ferrat, F. Tzompantzia , A. López-Ortega, E. Romero, E. Ortiz-Islas, R.Gómez, and M. Torres; Chemm. Com., 13,1498-1499 (2004)..14. M. Golombok and J. de Brujin; Ind. Eng. Chem. Res., 39, 267-271(2000).15. L.O. Stine and S.C. Gimre, US Pat 5,856,604, to UOP LLC (1999).16. M. Torres, L. Lopez, J. Domínguez, A. Mantilla, G. Ferrat, M. Gutiérrez and M.Maubert. Chem. Eng. J., 92, 1-6 (2003).17. M. Golombok and J. de Brujin. Ind. Eng. Chem. Res., 39, 267-271(2000).18. M. Marchionna, M. Di Girolamo and R. Patrini, R., Catal. Today, 65, 397-403(2001).19. M. Golombok and J. De Bruijn, J.App. Catal. A: General, 208, 47-53 (2001).20. E. López, A. Mantilla, G. Ferrat and A. López y Mario Vera. Petrol. Sci. andTechnol., 177-187 (2004.).21. R. Alcántara, E. Alcántara, L. Canoira, M.J. Franco. M. Herrera and A.Navarro. Reactive & Functional Polymers, 45, 19-27 (2000).22. X. Bokhimi, A. Morales, E. Ortíz, T. López, R. Gómez and J. Navarrete, J. Sol-Gel Sci. Technol., 29, 31 (2004).
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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
Page 42 and 43: Moses et al. 15perrhenate, followed
Page 44 and 45: Moses et al. 17SnCOSnMe 4≡SiOReO
Page 46 and 47: Moses et al. 19(AlOSi) of the cube.
Page 48 and 49: Moses et al. 212.510 3 k obs / s -1
Page 50 and 51: Wang et al. 233. Catalytic Hydrogen
Page 52 and 53: Wang et al. 25The rate expressions
Page 54 and 55: Wang et al. 27Schiff’s base forma
Page 56: Wang et al. 29AcknowledgementsWe gr
Page 59 and 60: 32Halophosphite LigandsIn 1970, Pru
Page 61 and 62: 34Halophosphite LigandsThe ligands,
Page 63 and 64: 36Halophosphite LigandsTable 2 Temp
Page 65 and 66: 38Halophosphite Ligands3. P. W. N.
Page 67 and 68: 40Monolithic Bioreactorstrength for
Page 69 and 70: 42Monolithic BioreactorMenten equat
Page 72 and 73: Gőbölös et al. 456. Highly Selec
Page 74 and 75: Gőbölös et al. 47was practically
Page 76 and 77: Gőbölös et al. 49noteworthy that
Page 78 and 79: Gőbölös et al. 51Figure 2 NMR sp
Page 80: Gőbölös et al. 53internal TMS in
Page 83 and 84: 56Hydrotalcite-like Catalysts[A n-
Page 85 and 86: 58Hydrotalcite-like Catalystssample
Page 88 and 89: Mantilla, Tzompantzi, Torres and G
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Page 94 and 95: Canning, Gamman, Jackson and Urquar
Page 102: Canning, Gamman, Jackson and Urquar
Page 105 and 106: 78Methylation of Catecholthe use of
Page 107 and 108: 80Methylation of CatecholThe main r
Page 110 and 111: Ardizzi et al. 8311. The Environmen
Page 112 and 113: Ardizzi et al. 85the selectivity to
Page 114: Ardizzi et al. 87Experimental Secti
Page 118 and 119: Hu et al. 9112. Biphasic Catalytic
Page 120 and 121: Hu et al. 93Results and DiscussionM
Page 122 and 123: Hu et al. 95ionic liquid is used in
Page 124 and 125: Hu et al. 97Figure 4. Schematic flo
Page 126 and 127: Singh and Chuang 9913. Reaction Pat
Page 128 and 129: Singh and Chuang 101for O 2 , 40 fo
Page 130 and 131: Singh and Chuang 103537373650Temp (
Page 132 and 133: Singh and Chuang 1050.064m/e = 32 (
Page 134 and 135: Singh and Chuang 107In summary, hyd
Page 136 and 137: Bacchini et al . 10914. The Transfo
Page 138 and 139: Bacchini et al . 1111 summarizes th
Page 140 and 141: Bacchini et al . 113these samples h
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Bacchini et al . 115around 1. The d
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Bacchini et al . 117Experimental Se
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Tanielyan et al. 11915. Transition
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Tanielyan et al. 121We wish to repo
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Tanielyan et al. 123Fig 1a shows th
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Tanielyan et al. 125TEMPO concentra
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Tanielyan et al. 127complete conver
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Tanielyan et al. 129ConclusionsIt h
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Liu, Cant and Smith 13116. The Conv
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Liu, Cant and Smith 133calculated f
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Liu, Cant and Smith 135Table 3. App
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Liu, Cant and Smith 137noting that
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Liu, Cant and Smith 139an exact fit
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Tanielyan et al. 14117. Bromine-Fre
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Tanielyan et al. 143TEMPO catalyst,
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mmol),Tanielyan et al. 145catalyst.
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Miller and Chuang 14718. In situ In
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Miller and Chuang 1492(a)2359217516
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Miller and Chuang 151(a)33802973292
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III. Symposium on Catalytic Hydroge
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156 Raney® Metastable PrecursorsIn
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158 Raney® Metastable Precursorsfe
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160 Raney® Metastable Precursorssl
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162 Raney® Metastable Precursorsfu
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164 Raney® Metastable Precursorsva
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Gelder, Jackson and Lok 16720. Comp
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Gelder, Jackson and Lok 169hydrogen
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Gelder, Jackson and Lok 171more rap
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Gelder, Jackson and Lok 173and that
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Gelder, Jackson and Lok 175measured
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Nikoshvili et al . 17721. Selective
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Nikoshvili et al . 179Experimental
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Nikoshvili et al . 181gasometrical
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Nikoshvili et al . 183causes the se
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Nikoshvili et al . 185determined th
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Salmi et al. 18722. Modeling and Op
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Salmi et al. 189andn−1( ) ( 1)) 1
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Salmi et al. 191dci= Niap− NGLiaG
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Salmi et al. 193of adsorption and t
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Salmi et al. 195Notationaa pa GLAcd
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Ostgard et al . 19723. The Effects
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Ostgard et al . 199not the ionic sa
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Ostgard et al . 201-2-0,9 -0,7 -0,5
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Ostgard et al . 2032,22Figure 8 NiM
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Ostgard et al . 205Max Act., mol/(m
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Ostgard et al . 207Flat Adsorbtion
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Ostgard et al . 209product mixture.
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Ostgard et al . 2116. M. Makkee, A.
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214 Cavitating Ultrasound Hydrogena
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228 Hydrogenation of Pynitrilesuch
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230 Hydrogenation of Pynitrile%Sele
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232 Hydrogenation of Pynitrile%Sele
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234 Hydrogenation of Pynitrile10. A
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236Deactivation of Catalyst in Suga
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238Deactivation of Catalyst in Suga
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Jackson and Spence 24127. Selectivi
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Jackson and Spence 243been related
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Jackson and Spence 245Acknowledgeme
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248Homogeneous Hydrogenationthe pre
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250Homogeneous Hydrogenationmetal s
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252Homogeneous Hydrogenation2. R. R
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254 Amination of Isobutanolnotewort
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256 Amination of Isobutanoland (iBu
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259IV. Symposium on Novel Methods i
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262Find the Best Catalystquantitati
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264Find the Best CatalystSTARTcreat
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266Find the Best CatalystNHNPNO NNC
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268Find the Best CatalystFigure 4.
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270Find the Best Catalyst14. For a
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272 Acidic Ionic LiquidsThe effect
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274 Acidic Ionic Liquidssites for H
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276 Acidic Ionic Liquids102.2 ppm 9
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278 Acidic Ionic LiquidsClClClClClC
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280 Acidic Ionic Liquids9. E. J. An
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282 Chemoselective Hydrogenationthe
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284 Chemoselective HydrogenationThe
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286 Chemoselective HydrogenationCNN
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288 Chemoselective Hydrogenation11.
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290 Hydrogenolysis over Structured
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Pugin et al. 29334. Twinphos: A New
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Pugin et al. 295ferrocene binding m
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Pugin et al. 297complexes with one
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Pugin et al. 2993: 50.1 (J pp =50 H
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Pugin et al. 301temperature, then t
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Margitfalvi et al. 30335. Catalyst
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Margitfalvi et al. 305Based on the
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Margitfalvi et al. 307Table 1. Vari
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Margitfalvi et al. 309Combination o
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Margitfalvi et al. 311Figure 1. Map
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Margitfalvi et al. 313Acknowledgeme
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Auten, Crump, Singh and Chandler 31
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Falling et al. 32737. Development o
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Falling et al. 329With these proces
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Falling et al. 331salt, TOP18 has v
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Falling et al. 333The catalyst syst
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Falling et al. 335Normal operation
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Bianchi, Borzatta, Poluzzi and Vacc
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Griffin, Johnston, Prétôt and van
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356Synthesis of PseudoiononesOOO- H
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358Synthesis of PseudoiononesMgO Pe
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360Synthesis of Pseudoionones0.5 wt
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362Synthesis of PseudoiononesTable
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364Synthesis of Pseudoiononesstrong
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366 MIBK Synthesis via CDproduce me
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368 MIBK Synthesis via CDExperiment
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370 MIBK Synthesis via CDreboiler p
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372 MIBK Synthesis via CDIn MIBK, t
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374 MIBK Synthesis via CDConclusion
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Sanders et al. 37742. Producing Pol
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Sanders et al. 379For the purposes
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Sanders et al. 381corresponding alc
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Sanders et al. 383polyurethane foam
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Zoeller and Barnette 38543. Carbony
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Zoeller and Barnette 387The first s
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Zoeller and Barnette 389Material ac
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Zoeller and Barnette 391above 120°
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Zoeller and Barnette 393tributyl am
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Hallett, Pollet, Eckert and Liotta
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Kiss, Rothenberg and Dimian 40545.
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Kiss, Rothenberg and Dimian 407C 10
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Kiss, Rothenberg and Dimian 409Tabl
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Kiss, Rothenberg and Dimian 411X (m
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Kiss, Rothenberg and Dimian 413Prep
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Snåre et al. 41546. Continuous Deo
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Snåre et al. 417The production of
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Snåre et al. 419was 15 μm and the
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Snåre et al. 421to 13% of conversi
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Snåre et al. 423Ethyl stearate con
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Snåre et al. 425increase in the fo
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428Glycerol Hydrogenolysisfundament
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430Glycerol Hydrogenolysisreaction
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432Glycerol Hydrogenolysisexpense o
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434Glycerol Hydrogenolysis[GO], M1.
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436Glycerol HydrogenolysisReference
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438Sustainable Process Technologyth
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440Sustainable Process Technologyco
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442Sustainable Process Technologywi
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444Sustainable Process TechnologyTh
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Lee, Shi, Subramaniam and Busch 447
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VII. Symposium on Other Topics in C
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...456Chiral BisphospholanesToday,
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458Chiral BisphospholanesFirst, the
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460Chiral BisphospholanesInterestin
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Augustine, Tanielyan, Marin and Alv
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Knifton and Sanderson 46952. Select
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Knifton and Sanderson 4711414141413
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Knifton and Sanderson 4733. O. C. A
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476 Palladium LeachingResults and D
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478 Palladium Leachingtemperatures
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Arunajatesan, Cruz, Möbus and Chen
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488Profiling of Catalytic Performan
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494 Transition Metal Removalmetal r
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496 Transition Metal RemovalDeloxan
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498 Transition Metal Removalreduced
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Durán Pachón and Rothenberg 50157
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Durán Pachón and Rothenberg 503th
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Durán Pachón and Rothenberg 505Ac
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508Author IndexDíez Verónica K. 4
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510Author IndexPhillips Gerald W. 3
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Catalysis of Organic Reactions 513K
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Catalysis of Organic Reactions 515c
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Catalysis of Organic Reactions 517h
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Catalysis of Organic Reactions 519p
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