Recent advances in selective acetylene hydrogenation using palladium containing catalysts
Recent advances with Pd containing catalysts for the selective hydrogenation of acetylene are described. The overview classifies enhancement of catalytic properties for monometallic and bimetallic Pd catalysts. Activity/selectivity of Pd catalysts can be modified by controlling particle shape/morpho...
Saved in:
Published in | Frontiers of chemical science and engineering Vol. 9; no. 2; pp. 142 - 153 |
---|---|
Main Authors | , |
Format | Journal Article |
Language | English |
Published |
Beijing
Higher Education Press
01.06.2015
|
Subjects | |
Online Access | Get full text |
ISSN | 2095-0179 2095-0187 |
DOI | 10.1007/s11705-015-1516-4 |
Cover
Loading…
Abstract | Recent advances with Pd containing catalysts for the selective hydrogenation of acetylene are described. The overview classifies enhancement of catalytic properties for monometallic and bimetallic Pd catalysts. Activity/selectivity of Pd catalysts can be modified by controlling particle shape/morphology or immobilisation on a support which interacts strongly with Pd particles. In both cases enhanced ethylene selectivity is generally associated with modifying ethylene adsorption strength and/or changes to hydride formation. Inorganic and organic selectivity modifiers (i.e., species adsorbed onto Pd particle surface) have also been shown to enhance ethylene selectivity. Inorganic modifiers such as TiO
2
change Pd ensemble size and modify ethylene adsorption strength whereas organic modifiers such as diphenylsulfide are thought to create a surface template effect which favours acetylene adsorption with respect to ethylene. A number of metals and synthetic approaches have been explored to prepare Pd bimetallic catalysts. Examples where enhanced selectivity is observed are generally associated with decreased Pd ensemble size and/or hindering of the ease with which an unselective hydride phase is formed for Pd. A final class of bimetallic catalysts are discussed where Pd is not thought to be the primary reaction site but merely acts as a site where hydrogen dissociation and spillover occurs onto a second metal (Cu or Au) where the reaction takes place more selectively. |
---|---|
AbstractList | Recent advances with Pd containing catalysts for the selective hydrogenation of acetylene are described. The overview classifies enhancement of catalytic properties for monometallic and bimetallic Pd catalysts. Activity/selectivity of Pd catalysts can be modified by controlling particle shape/morphology or immobilisation on a support which interacts strongly with Pd particles. In both cases enhanced ethylene selectivity is generally associated with modifying ethylene adsorption strength and/or changes to hydride formation. Inorganic and organic selectivity modifiers (i.e., species adsorbed onto Pd particle surface) have also been shown to enhance ethylene selectivity. Inorganic modifiers such as TiO
2
change Pd ensemble size and modify ethylene adsorption strength whereas organic modifiers such as diphenylsulfide are thought to create a surface template effect which favours acetylene adsorption with respect to ethylene. A number of metals and synthetic approaches have been explored to prepare Pd bimetallic catalysts. Examples where enhanced selectivity is observed are generally associated with decreased Pd ensemble size and/or hindering of the ease with which an unselective hydride phase is formed for Pd. A final class of bimetallic catalysts are discussed where Pd is not thought to be the primary reaction site but merely acts as a site where hydrogen dissociation and spillover occurs onto a second metal (Cu or Au) where the reaction takes place more selectively. |
Author | Anderson, James A. McCue, Alan J. |
Author_xml | – sequence: 1 givenname: Alan J. surname: McCue fullname: McCue, Alan J. email: a.mccue@abdn.ac.uk organization: Surface Chemistry and Catalysis Group, Department of Chemistry, University of Aberdeen – sequence: 2 givenname: James A. surname: Anderson fullname: Anderson, James A. email: j.anderson@abdn.ac.uk organization: Surface Chemistry and Catalysis Group, Department of Chemistry, University of Aberdeen, Materials and Chemical Engineering Group, School of Engineering, University of Aberdeen |
BookMark | eNp9kM9KAzEQh4NUsNY-gLd9gdUku9nsHqX4DwqC6MFTmE5ma2SbLUla2Ld3a8WDh55m-DHfMPNdsonvPTF2LfiN4FzfRiE0VzkXKhdKVHl5xqaSN4ek1pO_XjcXbB6jW_FCyKootJ6yj1dC8ikDuwePFDPns0gdYXJ7ygApDR15yj4HG_o1eUiu99kuOr_OttB1YN1uk2HvEzh_CBESdENM8Yqdt9BFmv_WGXt_uH9bPOXLl8fnxd0yx5LrlJNFi7jiuuSNLGwLpeJVha1QtoFatoBtoyplteUIjS2kVVLXdS1sS1hILGZMH_di6GMM1Bp06efMFMB1RnBzkGSOkswoyRwkmXIkxT9yG9wGwnCSkUcmjrN-TcF89bvgxwdPQN9iOX5M |
CitedBy_id | crossref_primary_10_1039_D4NR01939C crossref_primary_10_1021_acscatal_0c00808 crossref_primary_10_1016_j_mcat_2021_112012 crossref_primary_10_2139_ssrn_3998954 crossref_primary_10_1002_adfm_202212097 crossref_primary_10_1063_1674_0068_30_cjcp1704082 crossref_primary_10_1016_j_mcat_2022_112535 crossref_primary_10_1021_acsmaterialsau_1c00080 crossref_primary_10_1134_S1070363220060298 crossref_primary_10_1016_j_apcata_2020_117627 crossref_primary_10_1007_s11705_022_2158_y crossref_primary_10_1002_cctc_201801430 crossref_primary_10_1039_D4TA02342K crossref_primary_10_3390_cryst13091356 crossref_primary_10_1002_smll_202005571 crossref_primary_10_1038_srep42172 crossref_primary_10_1002_anie_202100814 crossref_primary_10_1016_j_joei_2025_102064 crossref_primary_10_1016_j_apsusc_2024_161516 crossref_primary_10_1016_j_ces_2021_116939 crossref_primary_10_1016_j_cattod_2024_114877 crossref_primary_10_1016_j_susc_2022_122197 crossref_primary_10_1002_anie_202317710 crossref_primary_10_1016_j_jcat_2018_06_001 crossref_primary_10_1021_acs_jpcc_8b07181 crossref_primary_10_1021_acs_chemrev_9b00230 crossref_primary_10_1007_s10562_023_04555_0 crossref_primary_10_1016_j_apcata_2018_06_029 crossref_primary_10_1002_cctc_202401978 crossref_primary_10_1016_j_jcat_2018_03_019 crossref_primary_10_1002_ange_202009757 crossref_primary_10_1021_acsami_6b12653 crossref_primary_10_1016_j_cej_2021_134129 crossref_primary_10_1016_S1872_2067_22_64145_7 crossref_primary_10_1002_aic_18788 crossref_primary_10_3390_catal7110343 crossref_primary_10_1021_acs_jpcc_8b06880 crossref_primary_10_1002_anie_202421351 crossref_primary_10_1016_j_apsusc_2020_146493 crossref_primary_10_1016_j_jcat_2020_01_010 crossref_primary_10_1021_acssuschemeng_1c07263 crossref_primary_10_1007_s11051_019_4641_z crossref_primary_10_1039_D1CC00923K crossref_primary_10_1021_acsnano_2c06834 crossref_primary_10_1002_aic_18416 crossref_primary_10_1098_rsos_191155 crossref_primary_10_1515_revce_2016_0036 crossref_primary_10_1039_D2QI01664H crossref_primary_10_1016_j_mencom_2024_09_030 crossref_primary_10_1021_acscatal_7b01368 crossref_primary_10_1021_acs_jpcc_7b01227 crossref_primary_10_1039_C7CP01207A crossref_primary_10_18412_1816_0387_2022_6_51_67 crossref_primary_10_1002_anie_202109538 crossref_primary_10_1021_acscatal_1c00804 crossref_primary_10_1002_smll_202300956 crossref_primary_10_1016_j_mencom_2016_11_014 crossref_primary_10_1016_j_jcat_2024_115600 crossref_primary_10_1021_acscatal_0c03897 crossref_primary_10_1134_S0023158418060113 crossref_primary_10_1021_acs_iecr_9b02784 crossref_primary_10_1016_j_cplett_2020_137871 crossref_primary_10_1021_acs_jpcc_1c03157 crossref_primary_10_1016_j_jcat_2019_12_027 crossref_primary_10_1016_j_apcata_2017_07_041 crossref_primary_10_1016_j_apcata_2023_119447 crossref_primary_10_1021_acsami_3c11935 crossref_primary_10_1039_C6CP07400F crossref_primary_10_1007_s11705_021_2113_3 crossref_primary_10_1021_acs_jpcc_5c01178 crossref_primary_10_1002_ange_202105931 crossref_primary_10_1021_acscatal_4c04462 crossref_primary_10_1007_s11244_018_1071_6 crossref_primary_10_1002_ange_202421351 crossref_primary_10_1007_s10562_021_03620_w crossref_primary_10_1016_j_apsusc_2021_150141 crossref_primary_10_1021_jacs_1c02471 crossref_primary_10_1016_S1872_2067_21_64036_6 crossref_primary_10_1021_acsanm_3c05787 crossref_primary_10_1021_acs_jpclett_8b02363 crossref_primary_10_1038_s41929_021_00657_3 crossref_primary_10_1007_s10853_022_07171_2 crossref_primary_10_1021_acscatal_0c01536 crossref_primary_10_3390_molecules25163735 crossref_primary_10_1016_j_ces_2022_117852 crossref_primary_10_1039_D4NR01911C crossref_primary_10_1016_j_jcat_2016_05_002 crossref_primary_10_1021_acscatal_2c04379 crossref_primary_10_1016_j_mcat_2021_111660 crossref_primary_10_1016_j_mencom_2019_09_023 crossref_primary_10_3390_catal10010115 crossref_primary_10_1016_j_cattod_2017_05_024 crossref_primary_10_1021_acscatal_8b00872 crossref_primary_10_1021_acsami_0c19329 crossref_primary_10_1021_acs_iecr_3c02952 crossref_primary_10_1007_s11172_024_4234_6 crossref_primary_10_1038_s41467_018_05052_4 crossref_primary_10_1021_acs_jpcc_7b06270 crossref_primary_10_1021_jacsau_1c00574 crossref_primary_10_1039_D1CC05202K crossref_primary_10_1016_j_cej_2015_09_118 crossref_primary_10_1021_acs_jpcc_9b04863 crossref_primary_10_1039_D1CC00062D crossref_primary_10_1070_RCR5017 crossref_primary_10_1002_smll_202005234 crossref_primary_10_1002_ange_202100814 crossref_primary_10_1021_acs_chemmater_3c03058 crossref_primary_10_1021_acs_jpcc_2c04567 crossref_primary_10_1134_S207005042303008X crossref_primary_10_1002_anie_202009757 crossref_primary_10_1007_s11705_018_1789_5 crossref_primary_10_1016_j_catcom_2024_106860 crossref_primary_10_1016_j_jcat_2024_115373 crossref_primary_10_1038_s41467_023_37821_1 crossref_primary_10_1002_anie_202105931 crossref_primary_10_1021_acscatal_6b03009 crossref_primary_10_1002_aic_17874 crossref_primary_10_1039_D2CY02077G crossref_primary_10_1134_S0023158419050069 crossref_primary_10_1021_acsami_2c02132 crossref_primary_10_1021_acscatal_7b02862 crossref_primary_10_1016_j_apsusc_2022_154497 crossref_primary_10_1016_j_mencom_2023_10_032 crossref_primary_10_1039_C9FD00122K crossref_primary_10_1016_j_apcata_2015_09_012 crossref_primary_10_1021_acsami_3c09531 crossref_primary_10_1021_acs_chemmater_9b04737 crossref_primary_10_1021_acsami_0c12437 crossref_primary_10_1134_S0965544124050165 crossref_primary_10_1016_j_jcat_2016_08_003 crossref_primary_10_1002_ange_202109538 crossref_primary_10_32362_2410_6593_2016_11_2_50_56 crossref_primary_10_1016_j_apcata_2015_09_016 crossref_primary_10_1016_j_fuel_2022_124118 crossref_primary_10_1021_acscatal_0c02158 crossref_primary_10_2139_ssrn_4139629 crossref_primary_10_1126_sciadv_abb7369 crossref_primary_10_1016_j_eng_2020_06_023 crossref_primary_10_1021_acsnano_8b00352 crossref_primary_10_1021_acscatal_9b05402 crossref_primary_10_1021_acsanm_1c01643 crossref_primary_10_1134_S207005042001002X crossref_primary_10_1038_s41467_021_24059_y crossref_primary_10_1016_j_mencom_2020_07_018 crossref_primary_10_1007_s11144_021_01993_y crossref_primary_10_1021_acs_chemrev_2c00733 crossref_primary_10_1134_S0012500823600736 crossref_primary_10_1039_C5CY01921D crossref_primary_10_1016_j_cej_2023_148238 crossref_primary_10_1039_C5FD00188A crossref_primary_10_1007_s11144_023_02449_1 crossref_primary_10_1007_s12274_022_4138_4 crossref_primary_10_1016_j_mcat_2023_113602 crossref_primary_10_59761_RCR5148 crossref_primary_10_1016_j_jcat_2022_10_016 crossref_primary_10_1038_s41467_024_54274_2 crossref_primary_10_1134_S0023158419060107 crossref_primary_10_18412_1816_0387_2023_6_17_51 crossref_primary_10_1016_j_seppur_2024_126463 crossref_primary_10_1039_D4CP00719K crossref_primary_10_1016_j_jcat_2018_05_018 crossref_primary_10_1016_j_apsusc_2021_152369 crossref_primary_10_1021_acs_chemrev_9b00662 crossref_primary_10_1016_j_surfin_2023_103255 crossref_primary_10_1021_acsnano_1c04602 crossref_primary_10_1039_D3IM00046J crossref_primary_10_3390_catal14050315 crossref_primary_10_1016_S1872_2067_24_60033_1 crossref_primary_10_1007_s11426_022_1597_y crossref_primary_10_3390_molecules28062572 crossref_primary_10_1021_acsmaterialslett_0c00139 crossref_primary_10_1002_cctc_202301268 crossref_primary_10_1021_acscatal_4c07524 crossref_primary_10_1039_D4QI03125C crossref_primary_10_1016_j_jcat_2017_09_004 crossref_primary_10_1134_S0023158418050154 crossref_primary_10_1080_2055074X_2018_1477315 crossref_primary_10_1002_adma_201801878 crossref_primary_10_1007_s11164_025_05505_8 crossref_primary_10_1039_D1SC03087F crossref_primary_10_1016_j_ijhydene_2022_09_252 crossref_primary_10_1016_j_checat_2023_100524 crossref_primary_10_1039_D0AN01303J crossref_primary_10_1021_acscatal_9b04467 crossref_primary_10_1039_D4CY00675E crossref_primary_10_1021_acsomega_1c06244 crossref_primary_10_1021_acs_iecr_1c03553 crossref_primary_10_1039_C8SC03178A crossref_primary_10_1007_s11144_021_02112_7 crossref_primary_10_1039_D1CP05353A crossref_primary_10_1021_acs_iecr_8b03627 crossref_primary_10_1039_D4RE00039K crossref_primary_10_1002_cctc_202400566 crossref_primary_10_1134_S0023158421020099 crossref_primary_10_1021_acs_iecr_3c04024 crossref_primary_10_1039_C5CY01401H crossref_primary_10_3390_catal12111484 crossref_primary_10_1080_00268976_2020_1820090 crossref_primary_10_1002_cctc_202201479 crossref_primary_10_1134_S0023158417060027 crossref_primary_10_1016_j_apsusc_2022_155086 crossref_primary_10_18412_1816_0387_2019_5_334_344 crossref_primary_10_1002_ange_202400122 crossref_primary_10_1021_acssuschemeng_1c07455 crossref_primary_10_1134_S2070050424700156 crossref_primary_10_1016_j_cjche_2023_06_012 crossref_primary_10_1002_ange_202317710 crossref_primary_10_1007_s10853_018_2009_x crossref_primary_10_1002_aic_17922 crossref_primary_10_3389_fchem_2020_581512 crossref_primary_10_1002_aic_18454 crossref_primary_10_1021_acscatal_2c04883 crossref_primary_10_1021_jacs_3c06514 crossref_primary_10_1016_j_diamond_2018_08_007 crossref_primary_10_1021_acs_chemrev_0c00582 crossref_primary_10_1016_j_jcat_2023_115103 crossref_primary_10_1016_j_fuel_2022_127131 crossref_primary_10_1016_j_jcat_2022_08_023 crossref_primary_10_1007_s12274_017_1701_5 crossref_primary_10_1002_anie_202400122 crossref_primary_10_1039_D0CP05285J crossref_primary_10_31857_S2686953523600356 crossref_primary_10_1134_S0023158420030209 crossref_primary_10_1021_acs_jpcc_1c08424 |
Cites_doi | 10.1016/S0920-5861(98)00184-9 10.1021/cs400267x 10.1016/j.molcata.2014.08.015 10.1016/j.cattod.2014.07.017 10.1039/c2cy00479h 10.1021/cs300224j 10.1039/C3CY00754E 10.1039/C5CY00065C 10.1016/S0166-9834(00)84168-8 10.1080/01614940802142102 10.1126/science.1155200 10.1021/jp062205l 10.1016/j.jcat.2011.10.010 10.1002/anie.200801923 10.1039/c3cc43511c 10.1016/j.jcat.2008.06.014 10.1016/j.jcat.2008.07.012 10.1070/RC2009v078n03ABEH003893 10.1021/jp9103799 10.1016/j.jcat.2008.06.013 10.1021/ar300225s 10.1016/j.jcat.2014.08.016 10.1016/j.apcata.2009.11.030 10.1021/jp056765g 10.1016/j.jcat.2011.05.003 10.3390/ma6072958 10.1016/0021-9517(75)90280-8 10.1002/adfm.200801439 10.1039/C5CY00253B 10.1016/j.jcat.2013.06.018 10.1016/j.jcat.2014.06.018 10.1039/c3cp51538a 10.1016/j.jcat.2009.10.019 10.1103/PhysRevLett.103.246102 10.1039/c0dt00010h 10.1021/jp209033s 10.1016/j.cattod.2011.06.025 10.1016/j.cattod.2011.09.037 10.1016/j.apcata.2006.04.027 10.1016/j.apcata.2005.01.048 10.1016/j.jcat.2010.04.018 10.1039/C0CC01742F 10.1002/cctc.201300569 10.1016/j.apcata.2010.11.008 10.1016/j.jcat.2013.05.027 10.1007/s00214-010-0800-0 10.1016/j.jcat.2007.02.019 10.1007/s10562-006-0041-y 10.1016/j.jcat.2011.03.022 10.1002/cctc.201200100 10.1016/j.apcata.2015.02.038 10.1016/j.molcata.2013.12.003 10.1016/S0926-860X(01)00758-X 10.1126/science.1215864 10.1039/c3nj01136d 10.1080/01614940500364909 10.1016/j.apcata.2013.10.024 10.1021/la201007m 10.1016/j.apcata.2011.04.048 10.1134/S0023158412020152 10.1016/j.apcata.2014.05.027 10.1016/j.cattod.2014.05.028 10.1016/j.catcom.2012.03.012 |
ContentType | Journal Article |
Copyright | Higher Education Press and Springer-Verlag Berlin Heidelberg 2015 |
Copyright_xml | – notice: Higher Education Press and Springer-Verlag Berlin Heidelberg 2015 |
DBID | AAYXX CITATION |
DOI | 10.1007/s11705-015-1516-4 |
DatabaseName | CrossRef |
DatabaseTitle | CrossRef |
DatabaseTitleList | |
DeliveryMethod | fulltext_linktorsrc |
Discipline | Engineering Chemistry |
EISSN | 2095-0187 |
EndPage | 153 |
ExternalDocumentID | 10_1007_s11705_015_1516_4 |
GroupedDBID | -EM .VR 06C 06D 0R~ 0VY 1-T 2J2 2JN 2JY 2KG 2KM 2LR 2~H 30V 4.4 406 408 40E 5VS 8UJ 95- 95. 95~ 96X AABHQ AACDK AAIAL AAJBT AAJKR AANZL AARHV AARTL AASML AATNV AATVU AAUYE AAYIU AAYQN AAYTO AAYZH ABAKF ABDZT ABECU ABFTV ABHQN ABJNI ABJOX ABKCH ABMQK ABNWP ABQBU ABSXP ABTEG ABTHY ABTKH ABTMW ABWNU ABXPI ACAOD ACBXY ACDTI ACGFS ACHSB ACHXU ACIWK ACKNC ACMDZ ACMLO ACOKC ACOMO ACPIV ACSNA ACZOJ ADHIR ADINQ ADKNI ADKPE ADRFC ADTPH ADURQ ADYFF ADZKW AEBTG AEFQL AEGNC AEJHL AEJRE AEKMD AEMSY AENEX AEOHA AEPYU AESKC AETLH AEVLU AEXYK AFBBN AFLOW AFQWF AFWTZ AFZKB AGAYW AGDGC AGJBK AGMZJ AGQEE AGQMX AGRTI AGWIL AGWZB AGYKE AHBYD AHKAY AHSBF AHYZX AIAKS AIGIU AIIXL AILAN AITGF AJBLW AJRNO AJZVZ ALMA_UNASSIGNED_HOLDINGS ALWAN AMKLP AMXSW AMYLF AOCGG ARMRJ AXYYD B-. BDATZ BGNMA CSCUP DDRTE DNIVK DPUIP EBLON EBS EIOEI EJD ESBYG FERAY FIGPU FINBP FNLPD FRRFC FSGXE FWDCC G-Y G-Z GGCAI GGRSB GJIRD GNWQR GQ6 GQ7 HF~ HMJXF HRMNR IJ- IKXTQ IWAJR IXD I~Z J-C JBSCW JZLTJ KOV LLZTM M4Y MA- NPVJJ NQJWS NU0 O9J P4S P9N PF0 PT4 QOR R89 ROL RSV S16 S3B SAP SCL SCM SHX SISQX SJYHP SNE SNPRN SNX SOHCF SOJ SPISZ SRMVM SSLCW STPWE SZN TSG TUC U2A UG4 UOJIU UTJUX UZXMN VC2 VFIZW W48 WK8 YLTOR Z7R Z7V Z7X Z7Y Z7Z ZMTXR ~A9 -SB -S~ AAPKM AAXDM AAYXX ABBRH ABDBE ABFSG ACSTC AEZWR AFDZB AFHIU AFOHR AHPBZ AHWEU AIXLP ATHPR AYFIA CAJEB CITATION Q-- U1G U5L |
ID | FETCH-LOGICAL-c407t-edcdccb0740923dfa45066cf15d9a82facf9565d7d0ca9d32d5278881dfec32c3 |
IEDL.DBID | U2A |
ISSN | 2095-0179 |
IngestDate | Thu Apr 24 22:53:42 EDT 2025 Tue Jul 01 02:11:17 EDT 2025 Fri Feb 21 02:33:36 EST 2025 |
IsDoiOpenAccess | false |
IsOpenAccess | true |
IsPeerReviewed | true |
IsScholarly | true |
Issue | 2 |
Keywords | palladium selective hydrogenation acetylene ethylene bimetallic |
Language | English |
LinkModel | DirectLink |
MergedId | FETCHMERGED-LOGICAL-c407t-edcdccb0740923dfa45066cf15d9a82facf9565d7d0ca9d32d5278881dfec32c3 |
OpenAccessLink | https://journal.hep.com.cn/fcse/EN/10.1007/s11705-015-1516-4 |
PageCount | 12 |
ParticipantIDs | crossref_citationtrail_10_1007_s11705_015_1516_4 crossref_primary_10_1007_s11705_015_1516_4 springer_journals_10_1007_s11705_015_1516_4 |
ProviderPackageCode | CITATION AAYXX |
PublicationCentury | 2000 |
PublicationDate | 2015-06-01 |
PublicationDateYYYYMMDD | 2015-06-01 |
PublicationDate_xml | – month: 06 year: 2015 text: 2015-06-01 day: 01 |
PublicationDecade | 2010 |
PublicationPlace | Beijing |
PublicationPlace_xml | – name: Beijing |
PublicationSubtitle | Selected Publications from Chinese Universities |
PublicationTitle | Frontiers of chemical science and engineering |
PublicationTitleAbbrev | Front. Chem. Sci. Eng |
PublicationYear | 2015 |
Publisher | Higher Education Press |
Publisher_xml | – name: Higher Education Press |
References | ArmbrüsterMBehrensMCinquiniFFöttingerKGrinYHaghoferAKlötzerBKnop-GerickeALorenzHOtaAPennerSPrinzJRameshanCRévayZRosenthalDRupprechterGTeschnerDTorresDWagnerRWidmerRWowsnickGHow to control the selectivity of palladium-based catalysts in hydrogenation reactions: The role of subsurface chemistryChemCatChem2012481048106310.1002/cctc.201200100 KhanN AShaikhutdinovSFreundH JAcetylene and ethylene hydrogenation on alumina supported Pd-Ag model catalystsCatalysis Letters20061083‐41591641:CAS:528:DC%2BD28XktVaqtbc%3D10.1007/s10562-006-0041-y FriedrichMVillasecaS ASzentmiklósiLTeschnerDArmbrüsterMOrder-induced selectivity increase of Cu60Pd40 in the semihydrogenation of acetyleneMaterials201367295829771:CAS:528:DC%2BC3sXht1WjsL7J10.3390/ma6072958 BridierBLopezNPérez-RamírezJMolecular understanding of alkyne hydrogenation for the design of selective catalystsDalton Transactions20103936841284191:CAS:528:DC%2BC3cXhtFWqt7%2FK10.1039/c0dt00010h SeguraYLópezNPérez-RamírezJOrigin of the superior hydrogenation selectivity of gold nanoparticles in alkyne + alkene mixtures: Triple-versus double-bond activationJournal of Catalysis200724723833861:CAS:528:DC%2BD2sXjvVans7g%3D10.1016/j.jcat.2007.02.019 Johnson M M, Walker D W, Nowack G P. U S Patent, 4404124A, 1983-09-13 García-MotaMGómez-DíazJNovell-LeruthGVargas-FuentesCBellarosaLBridierBPérez-RamírezJLópezNA density functional theory study of the “mythic” Lindlar hydrogenation catalystTheoretical Chemistry Accounts2011128466367310.1007/s00214-010-0800-0 Crespo-QuesadaMAndansonJ MYarulinALimBXiaYKiwi-MinskerLUV-ozone cleaning of supported poly(vinylpyrrolidone)-stabilized palladium nanocubes: Effect of stabilizer removal on morphology and catalytic behaviorLangmuir20112712790979161:CAS:528:DC%2BC3MXmt1Ghsb8%3D10.1021/la201007m YangBBurchRHardacreCHeaddockGHuPInfluence of surface structures, subsurface carbon and hydrogen, and surface alloying on the activity and selectivity of acetylene hydrogenation on Pd surfaces: A density functional theory studyJournal of Catalysis20133052642761:CAS:528:DC%2BC3sXhtFSmt7rK10.1016/j.jcat.2013.05.027 ShinEWKangJ HKimWJParkJ DMoonS HPerformance of Si-modified Pd catalyst in acetylene hydrogenation: The origin of the ethylene selectivity improvementApplied Catalysis A, General20022231–21611721:CAS:528:DC%2BD3MXptlCksrs%3D10.1016/S0926-860X(01)00758-X KyriakouGBoucherM BJewellA DLewisE ALawtonT JBaberA ETierneyH LFlytzani-StephanopoulosMSykesE C HIsolated metal atom geomretries as a strategy for selective heterogeneous hydrogenationsScience20123356073120912121:CAS:528:DC%2BC38XjtlKjsbk%3D10.1126/science.1215864 BoucherM BZugicBCladarasGKammertJMarcinkowskiM DLawtonT JSykesE C HFlytzani-StephanopoulosMSingle atom alloy surface analogs in Pd0.18Cu15 nanoparticles for selective hydrogenation reactionsPhysical Chemistry Chemical Physics2013152912187121961:CAS:528:DC%2BC3sXhtFSrt7jK10.1039/c3cp51538a FuQLuoYActive sites of Pd-doped flat and stepped Cu(111) surfaces for H2 dissociation in heterogeneous catalytic hydrogenationACS Catalysis201336124512521:CAS:528:DC%2BC3sXmslSntL4%3D10.1021/cs400267x PeiG XLiuX YWangALiLHuangYZhangTLeeJWJangB W LMouC YPromotional effect of Pd single atoms on Au nanoparticles supported on silica for the selective hydrogenation of acetylene in excess ethyleneNew Journal of Chemistry2014385204320511:CAS:528:DC%2BC2cXmtFSnu7g%3D10.1039/c3nj01136d BorodzińskiABondG CSelective hydrogenation of ethyne in ethene—rich streams on palladium catalysts. Part 2: Steady—state kinetics and effects of palladium particle size, carbon monoxide, and promotersCatalysis Reviews200850337946910.1080/01614940802142102 GulyaevaY KKaichevV VZaikovskiiV IKovalyovE VSuknevA PBal’zhinimaevB SSelective hydrogenation of acetylene over novel Pd/fiberglass catalystsCatalysis Today20152451391461:CAS:528:DC%2BC2cXhtFCgu7rN10.1016/j.cattod.2014.05.028 McCueA JAndersonJ ASulfur as a catalyst promoter or selectivity modifier in heterogeneous catalysisCatalysis Science & Technology2014422722941:CAS:528:DC%2BC2cXmt12htA%3D%3D10.1039/C3CY00754E LimBJiangMTaoJCamargoP H CZhuYXiaYShapecontrolled synthesis of Pd nanocrystals in aqueous solutionsAdvanced Functional Materials20091921892001:CAS:528:DC%2BD1MXhslequ7w%3D10.1002/adfm.200801439 RiyapanSBoonyongmaneeratYMekasuwandumrongOYoshidaHFujitaS IAraiMPanpranotJImproved catalytic performance of Pd/TiO2 in the selective hydrogenation of acetylene by using H2-treated sol-gel TiO2Journal of Molecular Catalysis A Chemical2014383–38418218710.1016/j.molcata.2013.12.003 TiedtkeD BCheungT T PLegerJZismanS ABergmeisterJ JDelzerG A13th Ethylene Producers Conference200110121 NikolaevS AZanaveskinI L NSmirnovV VAveryanovV AZanaveskinK ICatalytic hydrogenation of alkyne and alkadiene impurities from alkenes. Practical and theoretical aspectsRussian Chemical Reviews20097832312471:CAS:528:DC%2BD1MXotFKhuro%3D10.1070/RC2009v078n03ABEH003893 HanYPengDXuZWanHZhengSZhuDTiO2 supported Pd@Ag as highly selective catalysts for hydrogenation of acetylene in excess ethyleneChemical Communications20134975835083521:CAS:528:DC%2BC3sXhtlakurfP10.1039/c3cc43511c ShinE WChoiC HChangK SNaY HMoonS HProperties of Si-modified Pd catalyst for selective hydrogenation of acetyleneCatalysis Today19984431371431:CAS:528:DyaK1cXmt1Kmtb4%3D10.1016/S0920-5861(98)00184-9 YarulinA ECrespo-QuesadaR MEgorovaE VKiwi-MinskerL LStructure sensitivity of selective acetylene hydrogenation over the catalysts with shape-controlled palladium nanoparticlesKinetics and Catalysis20125322532611:CAS:528:DC%2BC38XkvVWrtbo%3D10.1134/S0023158412020152 Lopez-SanchezJ ALennonDThe use of titania- and iron oxide-supported gold catalysts for the hydrogenation of propyneApplied Catalysis A, General20052911–22302371:CAS:528:DC%2BD2MXosVajsro%3D10.1016/j.apcata.2005.01.048 SáJArteagaG DDaleyR ABernardiJAndersonJ AFactors influencing hydride formation in a Pd/TiO2 catalystJournal of Physical Chemistry B200611034170901709510.1021/jp062205l LudwigWSavaraAMadixR JSchauermannSFreundH JSubsurface hydrogen diffusion into Pd nanoparticles: Role of lowcoordinated surface sites and facilitation by carbonJournal of Physical Chemistry C20121165353935441:CAS:528:DC%2BC38Xpt1eg10.1021/jp209033s KimW JAhnI YLeeJ HMoonS HProperties of Pd/SiO2 catalyst doubly promoted with La oxide and Si for acetylene hydrogenationCatalysis Communications20122452551:CAS:528:DC%2BC38Xms1artLs%3D10.1016/j.catcom.2012.03.012 AhnI YKimW JMoonS HPerformance of La2O3- or Nb2O5-added Pd/SiO2 catalysts in acetylene hydrogenationApplied Catalysis A, General200630875811:CAS:528:DC%2BD28XlsFKqurg%3D10.1016/j.apcata.2006.04.027 OsswaldJKovnirKArmbrüsterMGiedigkeitRJentoftR EWildUGrinYSchlöglRPalladium-gallium intermetallic compounds for the selective hydrogenation of acetylene. Part II: Surface characterization and catalytic performanceJournal of Catalysis200825812192271:CAS:528:DC%2BD1cXptVKmtL4%3D10.1016/j.jcat.2008.06.014 WehrliJ TThomasD JWainwrightM STrimmD LCantN WSelective hydrogenation of propyne over supported copper catalysts: Influence of supportApplied Catalysis19917012532621:CAS:528:DyaK3MXktFaisbw%3D10.1016/S0166-9834(00)84168-8 TrimmD LLiuI O YCantN WThe selective hydrogenation of acetylene over a Ni/SiO2 catalyst in the presence and absence of carbon monoxideApplied Catalysis A, General20103741–258641:CAS:528:DC%2BC3cXnt12rsg%3D%3D10.1016/j.apcata.2009.11.030 HeY FFengJ TDuY YLiD QControllable synthesis and acetylene hydrogenation performance of supported pd nanowire and cuboctahedron catalystsACS Catalysis201228170317101:CAS:528:DC%2BC38Xps1Gjtr4%3D10.1021/cs300224j BridierBLópezNPérez-RamírezJPartial hydrogenation of propyne over copper-based catalysts and comparison with nickelbased analoguesJournal of Catalysis2010269180921:CAS:528:DC%2BD1MXhs1Wksr7P10.1016/j.jcat.2009.10.019 KimS KLeeJ HAhnI YKimW JMoonS HPerformance of Cu-promoted Pd catalysts prepared by adding Cu using a surface redox method in acetylene hydrogenationApplied Catalysis A, General20114011–212191:CAS:528:DC%2BC3MXotVGjurY%3D10.1016/j.apcata.2011.04.048 BorodzińskiABondG CSelective Hydrogenation of ethyne in ethene—rich streams on palladium catalysts. Part 1. Effect of changes to the catalyst during reactionCatalysis Reviews20064829114410.1080/01614940500364909 KimS KKimCLeeJ HKimJLeeHMoonS HPerformance of shape-controlled Pd nanoparticles in the selective hydrogenation of acetyleneJournal of Catalysis20133061461501:CAS:528:DC%2BC3sXht1Crsb3F10.1016/j.jcat.2013.06.018 RiyapanSBoonyongmaneeratYMekasuwandumrongOPraserthdamPPanpranotJEffect of surface Ti3+ on the sol-gel derived TiO2 in the selective acetylene hydrogenation on Pd/TiO2 catalystsCatalysis Today201424513413810.1016/j.cattod.2014.07.017 BurtonP DBoyleT JDatyeA KFacile. Surfactant-free synthesis of Pd nanoparticles for heterogeneous catalystsJournal of Catalysis201128021451491:CAS:528:DC%2BC3MXmvFWgsbk%3D10.1016/j.jcat.2011.03.022 SchauermannSNiliusNShaikhutdinovSFreundH JNanoparticles for heterogeneous catalysis: New mechanistic insightsAccounts of Chemical Research2013468167316811:CAS:528:DC%2BC38XhvVGrurrP10.1021/ar300225s BenavidezA DBurtonP DNogalesJ LJenkinsA RIvanovS AMillerJ TKarimA MDatyeA KImproved selectivity of carbonsupported palladium catalysts for the hydrogenaiton of acetylene in excess ethyleneApplied Catalysis A, General20144821081151:CAS:528:DC%2BC2cXhtF2kt7bE10.1016/j.apcata.2014.05.027 McKennaF MMantarosieLWellsR P KHardacreCAndersonJ ASelective hydrogenation of acetylene in ethylene rich feed streams at high pressure over ligand modified Pd/TiO2Catalysis Science & Technology2012236326381:CAS:528:DC%2BC38XjsFCrtbs%3D10.1039/c2cy00479h TeschnerDBorsodiJWootschARévayZHäveckerMKnop-GerickeAJacksonS DSchlöglRThe roles of subsurface carbon and hydrogen in palladium-catalyzed alkyne hydrogenationScience2008320587286891:CAS:528:DC%2BD1cXktVKhtrY%3D10.1126/science.1155200 GabaschHHayekKKlötzerBKnop-GerickeASchlöglRCarbon incorporation in Pd(111) by adsorption and dehydrogenation of etheneJournal of Physical Chemistry B M Wilde (1516_CR24) 2008; 47 M Crespo-Quesada (1516_CR30) 2011; 27 B Lim (1516_CR28) 2009; 19 Y Han (1516_CR51) 2013; 49 Q Fu (1516_CR63) 2013; 3 A J McCue (1516_CR64) 2015; 5 W Ludwig (1516_CR23) 2011; 284 N Cherkasov (1516_CR54) 2015; 497 M Friedrich (1516_CR57) 2013; 6 A Borodziński (1516_CR3) 2008; 50 M Armbrüster (1516_CR25) 2012; 4 D B Tiedtke (1516_CR1) 2001; 10 F M McKenna (1516_CR46) 2011; 281 S K Kim (1516_CR31) 2013; 306 D Teschner (1516_CR18) 2008; 320 M Boudart (1516_CR35) 1975; 39 S Abelló (1516_CR11) 2008; 259 F M McKenna (1516_CR48) 2011; 47 G Kyriakou (1516_CR60) 2012; 335 A J McCue (1516_CR47) 2014; 4 B Bridier (1516_CR6) 2010; 39 S Riyapan (1516_CR38) 2014; 245 A Borodziński (1516_CR2) 2006; 48 Y Segura (1516_CR7) 2007; 247 J Sá (1516_CR20) 2006; 110 A D Benavidez (1516_CR33) 2014; 482 C Ma (1516_CR53) 2014; 317 S A Nikolaev (1516_CR4) 2009; 78 J A Lopez-Sanchez (1516_CR14) 2005; 291 A J McCue (1516_CR62) 2014; 319 W J Kim (1516_CR41) 2012; 185 S Schauermann (1516_CR21) 2013; 46 Y F He (1516_CR32) 2012; 2 A J McCue (1516_CR50) 2015; 5 S Riyapan (1516_CR37) 2014; 383–384 G Vilé (1516_CR8) 2013; 5 H Gabasch (1516_CR17) 2006; 110 Y Zhang (1516_CR52) 2014; 469 E W Shin (1516_CR42) 1998; 44 M García-Mota (1516_CR15) 2010; 273 W Ludwig (1516_CR22) 2012; 116 D L Trimm (1516_CR12) 2010; 374 N A Khan (1516_CR26) 2006; 108 M B Boucher (1516_CR61) 2013; 15 B Bridier (1516_CR10) 2010; 269 P D Burton (1516_CR34) 2011; 280 D Teschner (1516_CR19) 2010; 114 Y Li (1516_CR39) 2011; 392 G X Pei (1516_CR65) 2014; 38 M García-Mota (1516_CR5) 2011; 128 W J Kim (1516_CR45) 2012; 24 I Y Ahn (1516_CR44) 2006; 308 J Osswald (1516_CR56) 2008; 258 1516_CR27 A E Yarulin (1516_CR29) 2012; 53 EW Shin (1516_CR43) 2002; 223 B Yang (1516_CR16) 2013; 305 Y K Gulyaeva (1516_CR36) 2015; 245 J T Wehrli (1516_CR9) 1991; 70 F M McKenna (1516_CR49) 2012; 2 H L Tierney (1516_CR59) 2009; 103 J Osswald (1516_CR55) 2008; 258 D L Trimm (1516_CR13) 2011; 178 S K Kim (1516_CR58) 2011; 401 B Zhu (1516_CR40) 2014; 395 |
References_xml | – reference: OsswaldJKovnirKArmbrüsterMGiedigkeitRJentoftR EWildUGrinYSchlöglRPalladium-gallium intermetallic compounds for the selective hydrogenation of acetylene. Part II: Surface characterization and catalytic performanceJournal of Catalysis200825812192271:CAS:528:DC%2BD1cXptVKmtL4%3D10.1016/j.jcat.2008.06.014 – reference: FuQLuoYActive sites of Pd-doped flat and stepped Cu(111) surfaces for H2 dissociation in heterogeneous catalytic hydrogenationACS Catalysis201336124512521:CAS:528:DC%2BC3sXmslSntL4%3D10.1021/cs400267x – reference: YarulinA ECrespo-QuesadaR MEgorovaE VKiwi-MinskerL LStructure sensitivity of selective acetylene hydrogenation over the catalysts with shape-controlled palladium nanoparticlesKinetics and Catalysis20125322532611:CAS:528:DC%2BC38XkvVWrtbo%3D10.1134/S0023158412020152 – reference: TrimmD LLiuI O YCantN WThe selective hydrogenation of acetylene over a Ni/SiO2 catalyst in the presence and absence of carbon monoxideApplied Catalysis A, General20103741–258641:CAS:528:DC%2BC3cXnt12rsg%3D%3D10.1016/j.apcata.2009.11.030 – reference: SeguraYLópezNPérez-RamírezJOrigin of the superior hydrogenation selectivity of gold nanoparticles in alkyne + alkene mixtures: Triple-versus double-bond activationJournal of Catalysis200724723833861:CAS:528:DC%2BD2sXjvVans7g%3D10.1016/j.jcat.2007.02.019 – reference: OsswaldJGiedigkeitRJentoftR EArmbrüsterMGirgsdiesFKovnirKResslerTGrinYSchlöglRPalladium-gallium intermetallic compounds for the selective hydrogenation of acetylene Part 1: Preparation and structural investigation under reaction conditionsJournal of Catalysis200825812102181:CAS:528:DC%2BD1cXptVKmt7c%3D10.1016/j.jcat.2008.06.013 – reference: BoudartMHwangH SSolubility of hydrogen in small particles of palladiumJournal of Catalysis197539144521:CAS:528:DyaE2MXkvVGns7Y%3D10.1016/0021-9517(75)90280-8 – reference: WildeMFukutaniKLudwigWBrandtBFischerJ HSchauermannSFreundH JInfluence of carbon deposition on the hydrogen distribution in Pd nanoparticles and their reactivity in olefin hydrogenationAngewandte Chemie International Edition20084748928992931:CAS:528:DC%2BD1cXhsVygtbrN10.1002/anie.200801923 – reference: LudwigWSavaraAMadixR JSchauermannSFreundH JSubsurface hydrogen diffusion into Pd nanoparticles: Role of lowcoordinated surface sites and facilitation by carbonJournal of Physical Chemistry C20121165353935441:CAS:528:DC%2BC38Xpt1eg10.1021/jp209033s – reference: AhnI YKimW JMoonS HPerformance of La2O3- or Nb2O5-added Pd/SiO2 catalysts in acetylene hydrogenationApplied Catalysis A, General200630875811:CAS:528:DC%2BD28XlsFKqurg%3D10.1016/j.apcata.2006.04.027 – reference: BenavidezA DBurtonP DNogalesJ LJenkinsA RIvanovS AMillerJ TKarimA MDatyeA KImproved selectivity of carbonsupported palladium catalysts for the hydrogenaiton of acetylene in excess ethyleneApplied Catalysis A, General20144821081151:CAS:528:DC%2BC2cXhtF2kt7bE10.1016/j.apcata.2014.05.027 – reference: McCueA JMcKennaF MAndersonJ ATriphenylphosphine: A ligand for heterogeneous catalysis too? Selectivity enhancement in acetylene hydrogenation over modified Pd/TiO2 catalystCatalysis Science & Technology201554244924591:CAS:528:DC%2BC2MXitlalu78%3D10.1039/C5CY00065C – reference: PeiG XLiuX YWangALiLHuangYZhangTLeeJWJangB W LMouC YPromotional effect of Pd single atoms on Au nanoparticles supported on silica for the selective hydrogenation of acetylene in excess ethyleneNew Journal of Chemistry2014385204320511:CAS:528:DC%2BC2cXmtFSnu7g%3D10.1039/c3nj01136d – reference: BridierBLópezNPérez-RamírezJPartial hydrogenation of propyne over copper-based catalysts and comparison with nickelbased analoguesJournal of Catalysis2010269180921:CAS:528:DC%2BD1MXhs1Wksr7P10.1016/j.jcat.2009.10.019 – reference: KimW JMoonS HModified Pd catalysts for the selective hydrogenation of acetyleneCatalysis Today201218512161:CAS:528:DC%2BC38XmtFCiur0%3D10.1016/j.cattod.2011.09.037 – reference: Johnson M M, Walker D W, Nowack G P. U S Patent, 4404124A, 1983-09-13 – reference: McKennaF MMantarosieLWellsR P KHardacreCAndersonJ ASelective hydrogenation of acetylene in ethylene rich feed streams at high pressure over ligand modified Pd/TiO2Catalysis Science & Technology2012236326381:CAS:528:DC%2BC38XjsFCrtbs%3D10.1039/c2cy00479h – reference: TrimmD LCantN WLiuI O YThe selective hydrogenation of acetylene in the presence of carbon monoxide over Ni and Ni-Zn supported on MgAl2O4Catalysis Today201117811811861:CAS:528:DC%2BC3MXhs1SqsLnK10.1016/j.cattod.2011.06.025 – reference: LudwigWSavaraADostertK HSchauermannSOlefin hydrogenation on Pd model supported catalysts: New mechanistic insightsJournal of Catalysis201128421481561:CAS:528:DC%2BC3MXhsFegurzM10.1016/j.jcat.2011.10.010 – reference: RiyapanSBoonyongmaneeratYMekasuwandumrongOPraserthdamPPanpranotJEffect of surface Ti3+ on the sol-gel derived TiO2 in the selective acetylene hydrogenation on Pd/TiO2 catalystsCatalysis Today201424513413810.1016/j.cattod.2014.07.017 – reference: BoucherM BZugicBCladarasGKammertJMarcinkowskiM DLawtonT JSykesE C HFlytzani-StephanopoulosMSingle atom alloy surface analogs in Pd0.18Cu15 nanoparticles for selective hydrogenation reactionsPhysical Chemistry Chemical Physics2013152912187121961:CAS:528:DC%2BC3sXhtFSrt7jK10.1039/c3cp51538a – reference: Lopez-SanchezJ ALennonDThe use of titania- and iron oxide-supported gold catalysts for the hydrogenation of propyneApplied Catalysis A, General20052911–22302371:CAS:528:DC%2BD2MXosVajsro%3D10.1016/j.apcata.2005.01.048 – reference: ZhangYDiaoWWilliamsC TMonnierJ RSelective hydrogenation of acetylene in excess ethylene using Ag- and Au-Pd/SiO2 bimetallic catalysts prepared by electroless depositionApplied Catalysis A, General20144694194261:CAS:528:DC%2BC3sXhvFWqur%2FP10.1016/j.apcata.2013.10.024 – reference: TeschnerDBorsodiJKisZSzentmiklósiLRévayZKnop-GerickeASchlöglRTorresDSautetPRole of hydrogen species in palladium-catalyzed alkyne hydrogenationJournal of Physical Chemistry C20101145229322991:CAS:528:DC%2BC3cXot1KntA%3D%3D10.1021/jp9103799 – reference: LimBJiangMTaoJCamargoP H CZhuYXiaYShapecontrolled synthesis of Pd nanocrystals in aqueous solutionsAdvanced Functional Materials20091921892001:CAS:528:DC%2BD1MXhslequ7w%3D10.1002/adfm.200801439 – reference: McKennaF MWellsR P KAndersonJ AEnhanced selectivity in acetylene hydrogenation by ligand modified Pd/TiO2 catalystsChemical Communications2011478235123531:CAS:528:DC%2BC3MXhs1art7g%3D10.1039/C0CC01742F – reference: TeschnerDBorsodiJWootschARévayZHäveckerMKnop-GerickeAJacksonS DSchlöglRThe roles of subsurface carbon and hydrogen in palladium-catalyzed alkyne hydrogenationScience2008320587286891:CAS:528:DC%2BD1cXktVKhtrY%3D10.1126/science.1155200 – reference: McCueA JAndersonJ ASulfur as a catalyst promoter or selectivity modifier in heterogeneous catalysisCatalysis Science & Technology2014422722941:CAS:528:DC%2BC2cXmt12htA%3D%3D10.1039/C3CY00754E – reference: García-MotaMBridierBPérez-RamírezJLópezNInterplay between carbon monoxide, hydrides, and carbides in selective alkyne hydrogenation on palladiumJournal of Catalysis201027329210210.1016/j.jcat.2010.04.018 – reference: McCueA JShepherdA MAndersonJ AOptimisation of preparation method for Pd coped Cu/Al2O3 catalysts for selective acetylene hydrogenationCatalysis Science & Technology201555288028901:CAS:528:DC%2BC2MXkvVKqurc%3D10.1039/C5CY00253B – reference: TierneyH LBaberA EKitchinJ RSykesE C HHydrogen dissociation and spillover on individual isolated palladium atomsPhysical Review Letters20091032424610224610410.1103/PhysRevLett.103.246102 – reference: KimW JAhnI YLeeJ HMoonS HProperties of Pd/SiO2 catalyst doubly promoted with La oxide and Si for acetylene hydrogenationCatalysis Communications20122452551:CAS:528:DC%2BC38Xms1artLs%3D10.1016/j.catcom.2012.03.012 – reference: BurtonP DBoyleT JDatyeA KFacile. Surfactant-free synthesis of Pd nanoparticles for heterogeneous catalystsJournal of Catalysis201128021451491:CAS:528:DC%2BC3MXmvFWgsbk%3D10.1016/j.jcat.2011.03.022 – reference: BorodzińskiABondG CSelective Hydrogenation of ethyne in ethene—rich streams on palladium catalysts. Part 1. Effect of changes to the catalyst during reactionCatalysis Reviews20064829114410.1080/01614940500364909 – reference: KhanN AShaikhutdinovSFreundH JAcetylene and ethylene hydrogenation on alumina supported Pd-Ag model catalystsCatalysis Letters20061083‐41591641:CAS:528:DC%2BD28XktVaqtbc%3D10.1007/s10562-006-0041-y – reference: ArmbrüsterMBehrensMCinquiniFFöttingerKGrinYHaghoferAKlötzerBKnop-GerickeALorenzHOtaAPennerSPrinzJRameshanCRévayZRosenthalDRupprechterGTeschnerDTorresDWagnerRWidmerRWowsnickGHow to control the selectivity of palladium-based catalysts in hydrogenation reactions: The role of subsurface chemistryChemCatChem2012481048106310.1002/cctc.201200100 – reference: GulyaevaY KKaichevV VZaikovskiiV IKovalyovE VSuknevA PBal’zhinimaevB SSelective hydrogenation of acetylene over novel Pd/fiberglass catalystsCatalysis Today20152451391461:CAS:528:DC%2BC2cXhtFCgu7rN10.1016/j.cattod.2014.05.028 – reference: SchauermannSNiliusNShaikhutdinovSFreundH JNanoparticles for heterogeneous catalysis: New mechanistic insightsAccounts of Chemical Research2013468167316811:CAS:528:DC%2BC38XhvVGrurrP10.1021/ar300225s – reference: ShinE WChoiC HChangK SNaY HMoonS HProperties of Si-modified Pd catalyst for selective hydrogenation of acetyleneCatalysis Today19984431371431:CAS:528:DyaK1cXmt1Kmtb4%3D10.1016/S0920-5861(98)00184-9 – reference: ZhuBJangB W LInsights into surface properties of non-thermal RF plasmas treated Pd/TiO2 in acetylene hydrogenationJournal of Molecular Catalysis A, Chemical20143951371441:CAS:528:DC%2BC2cXhsVGgt7vI10.1016/j.molcata.2014.08.015 – reference: McKennaF MAndersonJ ASelectivity enhancement in acetylene hydrogenation over diphenyl sulphide-modified Pd/TiO2 catalystsJournal of Catalysis201128122312401:CAS:528:DC%2BC3MXoslajur8%3D10.1016/j.jcat.2011.05.003 – reference: CherkasovNIbhadonA OMcCueA JAndersonJ AJohnstonS KPalladium-bismuth intermetallic and surface-poisoned catalysts for the semi-hydrogenation of 2-methyl-3-butyn-2-olApplied Catalysis A, General201549722301:CAS:528:DC%2BC2MXjslymtr4%3D10.1016/j.apcata.2015.02.038 – reference: RiyapanSBoonyongmaneeratYMekasuwandumrongOYoshidaHFujitaS IAraiMPanpranotJImproved catalytic performance of Pd/TiO2 in the selective hydrogenation of acetylene by using H2-treated sol-gel TiO2Journal of Molecular Catalysis A Chemical2014383–38418218710.1016/j.molcata.2013.12.003 – reference: TiedtkeD BCheungT T PLegerJZismanS ABergmeisterJ JDelzerG A13th Ethylene Producers Conference200110121 – reference: ShinEWKangJ HKimWJParkJ DMoonS HPerformance of Si-modified Pd catalyst in acetylene hydrogenation: The origin of the ethylene selectivity improvementApplied Catalysis A, General20022231–21611721:CAS:528:DC%2BD3MXptlCksrs%3D10.1016/S0926-860X(01)00758-X – reference: KimS KKimCLeeJ HKimJLeeHMoonS HPerformance of shape-controlled Pd nanoparticles in the selective hydrogenation of acetyleneJournal of Catalysis20133061461501:CAS:528:DC%2BC3sXht1Crsb3F10.1016/j.jcat.2013.06.018 – reference: GabaschHHayekKKlötzerBKnop-GerickeASchlöglRCarbon incorporation in Pd(111) by adsorption and dehydrogenation of etheneJournal of Physical Chemistry B200611010494749521:CAS:528:DC%2BD28Xhs1Sqt7k%3D10.1021/jp056765g – reference: BridierBLopezNPérez-RamírezJMolecular understanding of alkyne hydrogenation for the design of selective catalystsDalton Transactions20103936841284191:CAS:528:DC%2BC3cXhtFWqt7%2FK10.1039/c0dt00010h – reference: YangBBurchRHardacreCHeaddockGHuPInfluence of surface structures, subsurface carbon and hydrogen, and surface alloying on the activity and selectivity of acetylene hydrogenation on Pd surfaces: A density functional theory studyJournal of Catalysis20133052642761:CAS:528:DC%2BC3sXhtFSmt7rK10.1016/j.jcat.2013.05.027 – reference: McCueA JMcRitchieC JShepherdA MAndersonJ ACu/Al2O3 catalysts modified with Pd for selective acetylene hydrogenationJournal of Catalysis20143191271351:CAS:528:DC%2BC2cXhsFSjtL3M10.1016/j.jcat.2014.08.016 – reference: HanYPengDXuZWanHZhengSZhuDTiO2 supported Pd@Ag as highly selective catalysts for hydrogenation of acetylene in excess ethyleneChemical Communications20134975835083521:CAS:528:DC%2BC3sXhtlakurfP10.1039/c3cc43511c – reference: ViléGBaudouinDRemediakisI NCopéretCLópezNPérez-RamírezJSilver nanoparticles for olefin production: New insights into the mechanistic description of propyne hydrogenationChemCatChem20135123750375910.1002/cctc.201300569 – reference: HeY FFengJ TDuY YLiD QControllable synthesis and acetylene hydrogenation performance of supported pd nanowire and cuboctahedron catalystsACS Catalysis201228170317101:CAS:528:DC%2BC38Xps1Gjtr4%3D10.1021/cs300224j – reference: MaCDuYFengJCaoXYangJLiDFabrication of supported PdAu nanoflower catalyst for partial hydrogenation of acetyleneJournal of Catalysis20143172632711:CAS:528:DC%2BC2cXht1Khs7nF10.1016/j.jcat.2014.06.018 – reference: KimS KLeeJ HAhnI YKimW JMoonS HPerformance of Cu-promoted Pd catalysts prepared by adding Cu using a surface redox method in acetylene hydrogenationApplied Catalysis A, General20114011–212191:CAS:528:DC%2BC3MXotVGjurY%3D10.1016/j.apcata.2011.04.048 – reference: García-MotaMGómez-DíazJNovell-LeruthGVargas-FuentesCBellarosaLBridierBPérez-RamírezJLópezNA density functional theory study of the “mythic” Lindlar hydrogenation catalystTheoretical Chemistry Accounts2011128466367310.1007/s00214-010-0800-0 – reference: NikolaevS AZanaveskinI L NSmirnovV VAveryanovV AZanaveskinK ICatalytic hydrogenation of alkyne and alkadiene impurities from alkenes. Practical and theoretical aspectsRussian Chemical Reviews20097832312471:CAS:528:DC%2BD1MXotFKhuro%3D10.1070/RC2009v078n03ABEH003893 – reference: AbellóSVerboekendDBridierBPérez-RamírezJActivated takovite catalysts for partial hydrogenation of ethyne, propyne, and propadieneJournal of Catalysis20082591859510.1016/j.jcat.2008.07.012 – reference: Crespo-QuesadaMAndansonJ MYarulinALimBXiaYKiwi-MinskerLUV-ozone cleaning of supported poly(vinylpyrrolidone)-stabilized palladium nanocubes: Effect of stabilizer removal on morphology and catalytic behaviorLangmuir20112712790979161:CAS:528:DC%2BC3MXmt1Ghsb8%3D10.1021/la201007m – reference: WehrliJ TThomasD JWainwrightM STrimmD LCantN WSelective hydrogenation of propyne over supported copper catalysts: Influence of supportApplied Catalysis19917012532621:CAS:528:DyaK3MXktFaisbw%3D10.1016/S0166-9834(00)84168-8 – reference: KyriakouGBoucherM BJewellA DLewisE ALawtonT JBaberA ETierneyH LFlytzani-StephanopoulosMSykesE C HIsolated metal atom geomretries as a strategy for selective heterogeneous hydrogenationsScience20123356073120912121:CAS:528:DC%2BC38XjtlKjsbk%3D10.1126/science.1215864 – reference: BorodzińskiABondG CSelective hydrogenation of ethyne in ethene—rich streams on palladium catalysts. Part 2: Steady—state kinetics and effects of palladium particle size, carbon monoxide, and promotersCatalysis Reviews200850337946910.1080/01614940802142102 – reference: FriedrichMVillasecaS ASzentmiklósiLTeschnerDArmbrüsterMOrder-induced selectivity increase of Cu60Pd40 in the semihydrogenation of acetyleneMaterials201367295829771:CAS:528:DC%2BC3sXht1WjsL7J10.3390/ma6072958 – reference: SáJArteagaG DDaleyR ABernardiJAndersonJ AFactors influencing hydride formation in a Pd/TiO2 catalystJournal of Physical Chemistry B200611034170901709510.1021/jp062205l – reference: LiYJangB W LNon-thermal RF plasma effects on surface properties of Pd/TiO2 catalysts for selective hydrogenation of acetyleneApplied Catalysis A, General20113921–21731791:CAS:528:DC%2BC3MXjsV2itw%3D%3D10.1016/j.apcata.2010.11.008 – volume: 44 start-page: 137 issue: 3 year: 1998 ident: 1516_CR42 publication-title: Catalysis Today doi: 10.1016/S0920-5861(98)00184-9 – volume: 3 start-page: 1245 issue: 6 year: 2013 ident: 1516_CR63 publication-title: ACS Catalysis doi: 10.1021/cs400267x – volume: 395 start-page: 137 year: 2014 ident: 1516_CR40 publication-title: Journal of Molecular Catalysis A, Chemical doi: 10.1016/j.molcata.2014.08.015 – volume: 245 start-page: 134 year: 2014 ident: 1516_CR38 publication-title: Catalysis Today doi: 10.1016/j.cattod.2014.07.017 – volume: 2 start-page: 632 issue: 3 year: 2012 ident: 1516_CR49 publication-title: Catalysis Science & Technology doi: 10.1039/c2cy00479h – volume: 2 start-page: 1703 issue: 8 year: 2012 ident: 1516_CR32 publication-title: ACS Catalysis doi: 10.1021/cs300224j – volume: 4 start-page: 272 issue: 2 year: 2014 ident: 1516_CR47 publication-title: Catalysis Science & Technology doi: 10.1039/C3CY00754E – volume: 5 start-page: 2449 issue: 4 year: 2015 ident: 1516_CR50 publication-title: Catalysis Science & Technology doi: 10.1039/C5CY00065C – volume: 70 start-page: 253 issue: 1 year: 1991 ident: 1516_CR9 publication-title: Applied Catalysis doi: 10.1016/S0166-9834(00)84168-8 – volume: 50 start-page: 379 issue: 3 year: 2008 ident: 1516_CR3 publication-title: Catalysis Reviews doi: 10.1080/01614940802142102 – volume: 320 start-page: 86 issue: 5872 year: 2008 ident: 1516_CR18 publication-title: Science doi: 10.1126/science.1155200 – volume: 110 start-page: 17090 issue: 34 year: 2006 ident: 1516_CR20 publication-title: Journal of Physical Chemistry B doi: 10.1021/jp062205l – volume: 284 start-page: 148 issue: 2 year: 2011 ident: 1516_CR23 publication-title: Journal of Catalysis doi: 10.1016/j.jcat.2011.10.010 – volume: 47 start-page: 9289 issue: 48 year: 2008 ident: 1516_CR24 publication-title: Angewandte Chemie International Edition doi: 10.1002/anie.200801923 – volume: 49 start-page: 8350 issue: 75 year: 2013 ident: 1516_CR51 publication-title: Chemical Communications doi: 10.1039/c3cc43511c – volume: 258 start-page: 219 issue: 1 year: 2008 ident: 1516_CR56 publication-title: Journal of Catalysis doi: 10.1016/j.jcat.2008.06.014 – volume: 259 start-page: 85 issue: 1 year: 2008 ident: 1516_CR11 publication-title: Journal of Catalysis doi: 10.1016/j.jcat.2008.07.012 – volume: 78 start-page: 231 issue: 3 year: 2009 ident: 1516_CR4 publication-title: Russian Chemical Reviews doi: 10.1070/RC2009v078n03ABEH003893 – volume: 114 start-page: 2293 issue: 5 year: 2010 ident: 1516_CR19 publication-title: Journal of Physical Chemistry C doi: 10.1021/jp9103799 – volume: 258 start-page: 210 issue: 1 year: 2008 ident: 1516_CR55 publication-title: Journal of Catalysis doi: 10.1016/j.jcat.2008.06.013 – volume: 46 start-page: 1673 issue: 8 year: 2013 ident: 1516_CR21 publication-title: Accounts of Chemical Research doi: 10.1021/ar300225s – volume: 319 start-page: 127 year: 2014 ident: 1516_CR62 publication-title: Journal of Catalysis doi: 10.1016/j.jcat.2014.08.016 – volume: 374 start-page: 58 issue: 1–2 year: 2010 ident: 1516_CR12 publication-title: Applied Catalysis A, General doi: 10.1016/j.apcata.2009.11.030 – volume: 110 start-page: 4947 issue: 10 year: 2006 ident: 1516_CR17 publication-title: Journal of Physical Chemistry B doi: 10.1021/jp056765g – volume: 281 start-page: 231 issue: 2 year: 2011 ident: 1516_CR46 publication-title: Journal of Catalysis doi: 10.1016/j.jcat.2011.05.003 – volume: 6 start-page: 2958 issue: 7 year: 2013 ident: 1516_CR57 publication-title: Materials doi: 10.3390/ma6072958 – volume: 39 start-page: 44 issue: 1 year: 1975 ident: 1516_CR35 publication-title: Journal of Catalysis doi: 10.1016/0021-9517(75)90280-8 – volume: 19 start-page: 189 issue: 2 year: 2009 ident: 1516_CR28 publication-title: Advanced Functional Materials doi: 10.1002/adfm.200801439 – volume: 5 start-page: 2880 issue: 5 year: 2015 ident: 1516_CR64 publication-title: Catalysis Science & Technology doi: 10.1039/C5CY00253B – volume: 306 start-page: 146 year: 2013 ident: 1516_CR31 publication-title: Journal of Catalysis doi: 10.1016/j.jcat.2013.06.018 – volume: 10 start-page: 1 year: 2001 ident: 1516_CR1 publication-title: 13th Ethylene Producers Conference – volume: 317 start-page: 263 year: 2014 ident: 1516_CR53 publication-title: Journal of Catalysis doi: 10.1016/j.jcat.2014.06.018 – volume: 15 start-page: 12187 issue: 29 year: 2013 ident: 1516_CR61 publication-title: Physical Chemistry Chemical Physics doi: 10.1039/c3cp51538a – volume: 269 start-page: 80 issue: 1 year: 2010 ident: 1516_CR10 publication-title: Journal of Catalysis doi: 10.1016/j.jcat.2009.10.019 – volume: 103 start-page: 246102 issue: 24 year: 2009 ident: 1516_CR59 publication-title: Physical Review Letters doi: 10.1103/PhysRevLett.103.246102 – volume: 39 start-page: 8412 issue: 36 year: 2010 ident: 1516_CR6 publication-title: Dalton Transactions doi: 10.1039/c0dt00010h – volume: 116 start-page: 3539 issue: 5 year: 2012 ident: 1516_CR22 publication-title: Journal of Physical Chemistry C doi: 10.1021/jp209033s – volume: 178 start-page: 181 issue: 1 year: 2011 ident: 1516_CR13 publication-title: Catalysis Today doi: 10.1016/j.cattod.2011.06.025 – volume: 185 start-page: 2 issue: 1 year: 2012 ident: 1516_CR41 publication-title: Catalysis Today doi: 10.1016/j.cattod.2011.09.037 – volume: 308 start-page: 75 year: 2006 ident: 1516_CR44 publication-title: Applied Catalysis A, General doi: 10.1016/j.apcata.2006.04.027 – volume: 291 start-page: 230 issue: 1–2 year: 2005 ident: 1516_CR14 publication-title: Applied Catalysis A, General doi: 10.1016/j.apcata.2005.01.048 – volume: 273 start-page: 92 issue: 2 year: 2010 ident: 1516_CR15 publication-title: Journal of Catalysis doi: 10.1016/j.jcat.2010.04.018 – volume: 47 start-page: 2351 issue: 8 year: 2011 ident: 1516_CR48 publication-title: Chemical Communications doi: 10.1039/C0CC01742F – volume: 5 start-page: 3750 issue: 12 year: 2013 ident: 1516_CR8 publication-title: ChemCatChem doi: 10.1002/cctc.201300569 – volume: 392 start-page: 173 issue: 1–2 year: 2011 ident: 1516_CR39 publication-title: Applied Catalysis A, General doi: 10.1016/j.apcata.2010.11.008 – volume: 305 start-page: 264 year: 2013 ident: 1516_CR16 publication-title: Journal of Catalysis doi: 10.1016/j.jcat.2013.05.027 – volume: 128 start-page: 663 issue: 4 year: 2011 ident: 1516_CR5 publication-title: Theoretical Chemistry Accounts doi: 10.1007/s00214-010-0800-0 – volume: 247 start-page: 383 issue: 2 year: 2007 ident: 1516_CR7 publication-title: Journal of Catalysis doi: 10.1016/j.jcat.2007.02.019 – volume: 108 start-page: 159 issue: 3‐4 year: 2006 ident: 1516_CR26 publication-title: Catalysis Letters doi: 10.1007/s10562-006-0041-y – volume: 280 start-page: 145 issue: 2 year: 2011 ident: 1516_CR34 publication-title: Journal of Catalysis doi: 10.1016/j.jcat.2011.03.022 – volume: 4 start-page: 1048 issue: 8 year: 2012 ident: 1516_CR25 publication-title: ChemCatChem doi: 10.1002/cctc.201200100 – volume: 497 start-page: 22 year: 2015 ident: 1516_CR54 publication-title: Applied Catalysis A, General doi: 10.1016/j.apcata.2015.02.038 – volume: 383–384 start-page: 182 year: 2014 ident: 1516_CR37 publication-title: Journal of Molecular Catalysis A Chemical doi: 10.1016/j.molcata.2013.12.003 – volume: 223 start-page: 161 issue: 1–2 year: 2002 ident: 1516_CR43 publication-title: Applied Catalysis A, General doi: 10.1016/S0926-860X(01)00758-X – volume: 335 start-page: 1209 issue: 6073 year: 2012 ident: 1516_CR60 publication-title: Science doi: 10.1126/science.1215864 – volume: 38 start-page: 2043 issue: 5 year: 2014 ident: 1516_CR65 publication-title: New Journal of Chemistry doi: 10.1039/c3nj01136d – volume: 48 start-page: 91 issue: 2 year: 2006 ident: 1516_CR2 publication-title: Catalysis Reviews doi: 10.1080/01614940500364909 – volume: 469 start-page: 419 year: 2014 ident: 1516_CR52 publication-title: Applied Catalysis A, General doi: 10.1016/j.apcata.2013.10.024 – volume: 27 start-page: 7909 issue: 12 year: 2011 ident: 1516_CR30 publication-title: Langmuir doi: 10.1021/la201007m – volume: 401 start-page: 12 issue: 1–2 year: 2011 ident: 1516_CR58 publication-title: Applied Catalysis A, General doi: 10.1016/j.apcata.2011.04.048 – volume: 53 start-page: 253 issue: 2 year: 2012 ident: 1516_CR29 publication-title: Kinetics and Catalysis doi: 10.1134/S0023158412020152 – volume: 482 start-page: 108 year: 2014 ident: 1516_CR33 publication-title: Applied Catalysis A, General doi: 10.1016/j.apcata.2014.05.027 – volume: 245 start-page: 139 year: 2015 ident: 1516_CR36 publication-title: Catalysis Today doi: 10.1016/j.cattod.2014.05.028 – ident: 1516_CR27 – volume: 24 start-page: 52 year: 2012 ident: 1516_CR45 publication-title: Catalysis Communications doi: 10.1016/j.catcom.2012.03.012 |
SSID | ssib031263377 ssib011451075 ssib014623632 ssj0001844256 ssib020093015 ssib058688259 |
Score | 2.4547212 |
SecondaryResourceType | review_article |
Snippet | Recent advances with Pd containing catalysts for the selective hydrogenation of acetylene are described. The overview classifies enhancement of catalytic... |
SourceID | crossref springer |
SourceType | Enrichment Source Index Database Publisher |
StartPage | 142 |
SubjectTerms | Chemistry Chemistry and Materials Science Industrial Chemistry/Chemical Engineering Nanotechnology Review Article |
Title | Recent advances in selective acetylene hydrogenation using palladium containing catalysts |
URI | https://link.springer.com/article/10.1007/s11705-015-1516-4 |
Volume | 9 |
hasFullText | 1 |
inHoldings | 1 |
isFullTextHit | |
isPrint | |
link | http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwlV3NS8MwFA-6HdSD6FScHyMHT0qgSZq2OQ7ZHIqeHGyn0iapDrQba3fYf-9L1roNVLDXplBefsnvfT-EbkIWpKDZRiQEciC-oQFJNZPEMKmYzIRHjfVDPr8Eg6H_OBKjqo67qLPd65Cku6nXxW628wuYvoIASwXE30VNAaa7hfWQdWsQUTt61ltzItwEjAfr4kkbDeAbHMgpCzivijGdYybyAcduKJ1nq5cBsXU09Ke_2Oaz7WCq46j-ETqslEvcXaHhGO2YvIX27uuZbi10sNF-8ASNQWcEzsFVHkCBJzku3FwcuAJxoky5BE4y-H2p51MAmttEbDPl3_DMOuD1ZPGJbbL7aswEdr6gZVEWp2jY773eD0g1aoEosOhKYrTSSqWgT3ig8eks8QXoIiqjQsskYlmiMjCkhA61pxKpOdOCWeOZ6swozhQ_Q418mptzhG0gEd6lFCwVX0stgf2iMPPhMVSKtI28WmCxqvqQ23EYH_G6g7KVcQwyjq2MY7-Nbr8_ma2acPy1-K7ehbg6j8Xvqy_-tfoS7TO79c4Lc4Ua5XxhrkEpKdMOanYfxk-9jgPjF3Hv0kk |
linkProvider | Springer Nature |
linkToHtml | http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwlV07T8MwED5BOxQG3og3HphARolj5zEiVCi0MLUSnaLEdqACAiLpUH495zQhFAESWeNIyfni77s3wJHH3BiZrU89BAfKte3SWLGAahZIFiTCsrXxQ97cup0Bv74Td2Udd1Zlu1chyeKkrovdTOcXNH0FRZRyKZ-HJkcTXDSgeXY57LYrNbLN8FmrRkU8C5jj1uWTJh7gfEFBx2au45TlmIVrxueoycVYOsvUL6POVvHQn95jFtFmw6kFSl0sQ7_6vmlyyuPpOI9P5fu31o__FMAKLJWslZxN1WwV5nS6Bq3zaljcGix-6Wu4DkMkowhmpEwwyMgoJVkxcAfPVhJJnU8Q7DR5mKi3F9TgQjuIScG_J6_Gs69G42disuin8ytI4WSaZHm2AYOLdv-8Q8sZDlSiqZhTraSSMkaiYiGVVEnEBZIcmdhCBZHPkkgmaKEJ5SlLRoFymBLMWOW2SrR0mHQ2oZG-pHoLiIlQ4r3YRhOIq0AFCKu-l3C8tB2IeBusah9CWTY4N3M2nsK6NbORYIgSDI0EQ74Nx5-PvE67e_y1-KTal7D80bPfV-_8a_UhtDr9m17Yu7rt7sICM5tcuHr2oJG_jfU-Mp88Pig1_QOho_Bk |
linkToPdf | http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwlV1JS8NAFB60gstBtCrWdQ6elMHMTNZjqZa6FQ8W6ikks2hB09Kkh_5732QxLahgrplA8uZlvrd_CF14zI3BsvWJB-BAbEVdEksWEMUCwQLtWFSZOORT3-0N7PuhMyx5TtOq2r1KSRY9DWZKU5JdT6S-rhvfzBQYcIMdAojlEnsVrcFpTE1N14C1K4WihobWqvERTgXG3bqR0mQG-AIecspczsvGzDxI49ug0zlBnWU6mUF7q8zoT2-xjG3LidUcr7o7aLs0NHG70IxdtKKSJtroVPxuTbS1MIpwD72C_Qjfj8uagBSPEpzmHDlwHOJIqGwO-KTw-1xOx6B0-YZiUzX_hicmGC9Hs09spFhQTuA8LjRPs3QfDbq3L50eKWkXiADvLiNKCilEDLaFBdaf1JHtgF0iNHVkEPlMR0KDU-VIT1oiCiRn0mHGkaZSK8GZ4AeokYwTdYiwSSrCvZiC12LLQAaAhL6nbbgUDZy4haxKYKEoZ5IbaoyPsJ6mbGQcgoxDI-PQbqHL70cmxUCOvxZfVbsQlv9m-vvqo3-tPkfrzzfd8PGu_3CMNpnRgjw4c4Ia2XSmTsFWyeKzXB-_AKwT1-Q |
openUrl | ctx_ver=Z39.88-2004&ctx_enc=info%3Aofi%2Fenc%3AUTF-8&rfr_id=info%3Asid%2Fsummon.serialssolutions.com&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&rft.genre=article&rft.atitle=Recent+advances+in+selective+acetylene+hydrogenation+using+palladium+containing+catalysts&rft.jtitle=Frontiers+of+chemical+science+and+engineering&rft.au=McCue%2C+Alan+J.&rft.au=Anderson%2C+James+A.&rft.date=2015-06-01&rft.pub=Higher+Education+Press&rft.issn=2095-0179&rft.eissn=2095-0187&rft.volume=9&rft.issue=2&rft.spage=142&rft.epage=153&rft_id=info:doi/10.1007%2Fs11705-015-1516-4&rft.externalDocID=10_1007_s11705_015_1516_4 |
thumbnail_l | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/lc.gif&issn=2095-0179&client=summon |
thumbnail_m | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/mc.gif&issn=2095-0179&client=summon |
thumbnail_s | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/sc.gif&issn=2095-0179&client=summon |