Liquid-Phase Selective Hydrogenation of Hexa-1,5-diene and Hexa-1,3-diene on Palladium Catalysts. Effect of Tin and Silver Addition
Autor(a) principal: | |
---|---|
Data de Publicação: | 2000 |
Outros Autores: | , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Repositório Institucional da UFBA |
Texto Completo: | http://www.repositorio.ufba.br/ri/handle/ri/7282 |
Resumo: | p.96–105 |
id |
UFBA-2_25ec1be50b33e5c384f99f4e873c94ac |
---|---|
oai_identifier_str |
oai:repositorio.ufba.br:ri/7282 |
network_acronym_str |
UFBA-2 |
network_name_str |
Repositório Institucional da UFBA |
repository_id_str |
1932 |
spelling |
Sales, Emerson AndradeMendes, Mario de JesusBozon Verduraz, FrançoisSales, Emerson AndradeMendes, Mario de JesusBozon Verduraz, François2012-11-26T21:11:19Z2000-100021-9517http://www.repositorio.ufba.br/ri/handle/ri/7282v. 195, n. 1p.96–105The liquid-phase hydrogenation of hexa-1,5-diene and hexa-1,3-diene on alumina-supported palladium catalysts is investigated with special attention paid to the effects of tin or silver addition. All catalysts show a global selectivity near 100%; these high values persist at total conversion when the reactant is hexa-1,3-diene but decrease to about 70% in the case of hexa-1,5-diene. In the hexa-1,5-diene hydrogenation, monometallic palladium catalysts give mainly 1-hexene at conversions lower than 80% and E-hex-2-ene at higher conversions. The fractional selectivity to 1-hexene is significantly improved by tin or silver addition; however, significant yields are observed only on Pd–Sn catalysts with a low Sn/Pd atomic ratio (≈0.1) and when the intermetallic compound Pd3Sn is present. On the other hand, in the hexa-1,3-diene hydrogenation, hex-1-ene is preferentially formed on monometallic catalysts with low dispersion; on bimetallic Pd–Sn or Pd–Ag catalysts, the selectivity to E-hex-3-ene is enhanced and this isomer is even predominant up to 100% conversion on the Pd–Sn catalysts containing the Pd3Sn intermetallic compound. These results are explained by the geometric effect of dilution of Pd atoms, which delays the palladium double-bond isomerization ability. The proposed mechanism suggests that strongly adsorbed alkadienes react with dissolved hydrogen, following a zero-order kinetics.Submitted by Texeira Ana (atanateixeira@gmail.com) on 2012-11-26T21:11:19Z No. of bitstreams: 1 Sales.pdf: 136985 bytes, checksum: 5961256d3f993fde7dbd5534e9c9440b (MD5)Made available in DSpace on 2012-11-26T21:11:19Z (GMT). No. of bitstreams: 1 Sales.pdf: 136985 bytes, checksum: 5961256d3f993fde7dbd5534e9c9440b (MD5) Previous issue date: 2000-10Elsevierhttp://dx.doi.org/10.1006/jcat.2000.2966reponame:Repositório Institucional da UFBAinstname:Universidade Federal da Bahia (UFBA)instacron:UFBAPd catalystsPd–Sn catalystsPd–Ag catalystsSelective hydrogenationHexa-1,5-dieneHexa-1,3-dieneLiquid-Phase Selective Hydrogenation of Hexa-1,5-diene and Hexa-1,3-diene on Palladium Catalysts. Effect of Tin and Silver AdditionJournal of Catalysisinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/article10000-01-01enginfo:eu-repo/semantics/openAccessLICENSElicense.txtlicense.txttext/plain1762https://repositorio.ufba.br/bitstream/ri/7282/2/license.txt1b89a9a0548218172d7c829f87a0eab9MD52ORIGINALSales.pdfSales.pdfapplication/pdf136985https://repositorio.ufba.br/bitstream/ri/7282/1/Sales.pdf5961256d3f993fde7dbd5534e9c9440bMD51TEXTSales.pdf.txtSales.pdf.txtExtracted texttext/plain40484https://repositorio.ufba.br/bitstream/ri/7282/3/Sales.pdf.txt1a7529942e90e4520409ea40c26aa648MD53ri/72822022-07-05 14:03:10.987oai:repositorio.ufba.br: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Repositório InstitucionalPUBhttp://192.188.11.11:8080/oai/requestopendoar:19322022-07-05T17:03:10Repositório Institucional da UFBA - Universidade Federal da Bahia (UFBA)false |
dc.title.pt_BR.fl_str_mv |
Liquid-Phase Selective Hydrogenation of Hexa-1,5-diene and Hexa-1,3-diene on Palladium Catalysts. Effect of Tin and Silver Addition |
dc.title.alternative.pt_BR.fl_str_mv |
Journal of Catalysis |
title |
Liquid-Phase Selective Hydrogenation of Hexa-1,5-diene and Hexa-1,3-diene on Palladium Catalysts. Effect of Tin and Silver Addition |
spellingShingle |
Liquid-Phase Selective Hydrogenation of Hexa-1,5-diene and Hexa-1,3-diene on Palladium Catalysts. Effect of Tin and Silver Addition Sales, Emerson Andrade Pd catalysts Pd–Sn catalysts Pd–Ag catalysts Selective hydrogenation Hexa-1,5-diene Hexa-1,3-diene |
title_short |
Liquid-Phase Selective Hydrogenation of Hexa-1,5-diene and Hexa-1,3-diene on Palladium Catalysts. Effect of Tin and Silver Addition |
title_full |
Liquid-Phase Selective Hydrogenation of Hexa-1,5-diene and Hexa-1,3-diene on Palladium Catalysts. Effect of Tin and Silver Addition |
title_fullStr |
Liquid-Phase Selective Hydrogenation of Hexa-1,5-diene and Hexa-1,3-diene on Palladium Catalysts. Effect of Tin and Silver Addition |
title_full_unstemmed |
Liquid-Phase Selective Hydrogenation of Hexa-1,5-diene and Hexa-1,3-diene on Palladium Catalysts. Effect of Tin and Silver Addition |
title_sort |
Liquid-Phase Selective Hydrogenation of Hexa-1,5-diene and Hexa-1,3-diene on Palladium Catalysts. Effect of Tin and Silver Addition |
author |
Sales, Emerson Andrade |
author_facet |
Sales, Emerson Andrade Mendes, Mario de Jesus Bozon Verduraz, François |
author_role |
author |
author2 |
Mendes, Mario de Jesus Bozon Verduraz, François |
author2_role |
author author |
dc.contributor.author.fl_str_mv |
Sales, Emerson Andrade Mendes, Mario de Jesus Bozon Verduraz, François Sales, Emerson Andrade Mendes, Mario de Jesus Bozon Verduraz, François |
dc.subject.por.fl_str_mv |
Pd catalysts Pd–Sn catalysts Pd–Ag catalysts Selective hydrogenation Hexa-1,5-diene Hexa-1,3-diene |
topic |
Pd catalysts Pd–Sn catalysts Pd–Ag catalysts Selective hydrogenation Hexa-1,5-diene Hexa-1,3-diene |
description |
p.96–105 |
publishDate |
2000 |
dc.date.issued.fl_str_mv |
2000-10 |
dc.date.accessioned.fl_str_mv |
2012-11-26T21:11:19Z |
dc.type.status.fl_str_mv |
info:eu-repo/semantics/publishedVersion |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/article |
format |
article |
status_str |
publishedVersion |
dc.identifier.uri.fl_str_mv |
http://www.repositorio.ufba.br/ri/handle/ri/7282 |
dc.identifier.issn.none.fl_str_mv |
0021-9517 |
dc.identifier.number.pt_BR.fl_str_mv |
v. 195, n. 1 |
identifier_str_mv |
0021-9517 v. 195, n. 1 |
url |
http://www.repositorio.ufba.br/ri/handle/ri/7282 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
dc.publisher.none.fl_str_mv |
Elsevier |
publisher.none.fl_str_mv |
Elsevier |
dc.source.pt_BR.fl_str_mv |
http://dx.doi.org/10.1006/jcat.2000.2966 |
dc.source.none.fl_str_mv |
reponame:Repositório Institucional da UFBA instname:Universidade Federal da Bahia (UFBA) instacron:UFBA |
instname_str |
Universidade Federal da Bahia (UFBA) |
instacron_str |
UFBA |
institution |
UFBA |
reponame_str |
Repositório Institucional da UFBA |
collection |
Repositório Institucional da UFBA |
bitstream.url.fl_str_mv |
https://repositorio.ufba.br/bitstream/ri/7282/2/license.txt https://repositorio.ufba.br/bitstream/ri/7282/1/Sales.pdf https://repositorio.ufba.br/bitstream/ri/7282/3/Sales.pdf.txt |
bitstream.checksum.fl_str_mv |
1b89a9a0548218172d7c829f87a0eab9 5961256d3f993fde7dbd5534e9c9440b 1a7529942e90e4520409ea40c26aa648 |
bitstream.checksumAlgorithm.fl_str_mv |
MD5 MD5 MD5 |
repository.name.fl_str_mv |
Repositório Institucional da UFBA - Universidade Federal da Bahia (UFBA) |
repository.mail.fl_str_mv |
|
_version_ |
1808459411159515136 |