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VI. Symposium on “Green” <strong>Catalysis</strong>375
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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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Wang et al. 29AcknowledgementsWe gr
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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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100 Propylene Partial OxidationThe
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102 Propylene Partial OxidationSiO
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104 Propylene Partial Oxidation0.01
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106 Propylene Partial Oxidation0.02
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108 Propylene Partial OxidationRefe
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110Oxidation of n-Pentanemethacryli
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112Oxidation of n-PentaneFReqox1ox2
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114Oxidation of n-Pentanethe presen
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116Oxidation of n-PentaneIn the mec
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118Oxidation of n-PentaneReferences
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120TEMPO Oxidation of Alcoholsthe u
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122TEMPO Oxidation of AlcoholsThe r
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124TEMPO Oxidation of Alcoholsany d
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126TEMPO Oxidation of Alcoholsconce
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128TEMPO Oxidation of AlcoholsMNT :
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130TEMPO Oxidation of Alcoholsuptak
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132Aminoalcohols to Aminocarboxylic
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142Bromine-Free TEMPO-Based Catalys
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148CO OxidationP25 TiO 2 , respecti
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150CO Oxidation0.02(a)21802110(b)21
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152CO Oxidationcarboxylate species
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Yamauchi 15519. 2006 Murray Raney A
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Yamauchi 157transformation is schem
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Yamauchi 159The X-ray diffraction p
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Yamauchi 161was -0.0009, -0.0032 an
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Yamauchi 163shown in Fig. 12. It wa
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Yamauchi 165These fine particles we
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168Nitrobenzene Hydrogenationfurthe
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170Nitrobenzene Hydrogenationhydrog
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172Nitrobenzene HydrogenationThe co
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174Nitrobenzene HydrogenationHence
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176Nitrobenzene Hydrogenation10. G.
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178 Hydrogenation of Dehydrolinaloo
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188Modeling Mass Transfer Hydrogena
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198 Fructose HydrogenationHOHCCH 2O
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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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Page 355 and 356: 328Rearrangement of 3,4-Epoxy-1-But
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Page 373 and 374: 3462,5-Dimethyl-2,4-Hexadiene8. www
Page 375 and 376: 348Heteropoly AcidsSOOO O+ +OS1 2 3
Page 377 and 378: 350Heteropoly AcidsTable 3. Acylati
Page 379 and 380: 352Heteropoly AcidsSiO 2 is the bes
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Page 404 and 405: Sanders et al. 37742. Producing Pol
Page 406 and 407: Sanders et al. 379For the purposes
Page 408 and 409: Sanders et al. 381corresponding alc
Page 410 and 411: Sanders et al. 383polyurethane foam
Page 412 and 413: Zoeller and Barnette 38543. Carbony
Page 414 and 415: Zoeller and Barnette 387The first s
Page 416 and 417: Zoeller and Barnette 389Material ac
Page 418 and 419: Zoeller and Barnette 391above 120°
Page 420 and 421: Zoeller and Barnette 393tributyl am
Page 422 and 423: Hallett, Pollet, Eckert and Liotta
Page 432 and 433: Kiss, Rothenberg and Dimian 40545.
Page 434 and 435: Kiss, Rothenberg and Dimian 407C 10
Page 436 and 437: Kiss, Rothenberg and Dimian 409Tabl
Page 438 and 439: Kiss, Rothenberg and Dimian 411X (m
Page 440 and 441: Kiss, Rothenberg and Dimian 413Prep
Page 442 and 443: Snåre et al. 41546. Continuous Deo
Page 444 and 445: Snåre et al. 417The production of
Page 446 and 447: Snåre et al. 419was 15 μm and the
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Page 450 and 451: 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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