Continuously operated falling film microreactor for selective hydrogenation of carbon–carbon triple bonds

[Display omitted] •Process intensification with microstructured reactor equipment.•Continuous-flow gas–liquid–solid reaction.•Novel catalyst development with atomic layer deposition and PVP-Pd NPs.•Water as selectivity-enhancing and environmental friendly solvent. Despite significant advances in the...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Chemical engineering journal (Lausanne, Switzerland : 1996) Switzerland : 1996), 2016-06, Vol.293, p.345-354
Hauptverfasser: Rehm, Thomas H., Berguerand, Charline, Ek, Satu, Zapf, Ralf, Löb, Patrick, Nikoshvili, Linda, Kiwi-Minsker, Lioubov
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 354
container_issue
container_start_page 345
container_title Chemical engineering journal (Lausanne, Switzerland : 1996)
container_volume 293
creator Rehm, Thomas H.
Berguerand, Charline
Ek, Satu
Zapf, Ralf
Löb, Patrick
Nikoshvili, Linda
Kiwi-Minsker, Lioubov
description [Display omitted] •Process intensification with microstructured reactor equipment.•Continuous-flow gas–liquid–solid reaction.•Novel catalyst development with atomic layer deposition and PVP-Pd NPs.•Water as selectivity-enhancing and environmental friendly solvent. Despite significant advances in the fabrication and applications of microreactors for production of chemicals, their use for catalytic reactions remains a challenge, especially in fine chemical synthesis where the selectivity towards the desired product is an issue. A falling film microstructured reactor (FFMR) was tested in the selective hydrogenation of 2-butyne-1,4-diol (1) to its olefinic derivative (2). The FFMR plates were coated with Al2O3 or ZnO followed by the deposition of Pd nanoparticles (NPs). The oxides were deposited on the microstructured reaction plates using either conventional washcoating or atomic layer deposition (ALD) in the liquid or gas phase, respectively. The Pd-NPs were either formed via impregnation of an organometallic precursor with subsequent reduction, or with pre-fabricated Pd-NPs stabilized in poly(vinyl pyrrolidon) (PVP) with subsequent pyrolysis of the organic matrix and activation in H2 atmosphere. The palladium loading was varied in the range of 1.1–13.6wt%. Different solvents including water, 2-propanol and mixtures with organic bases were tested aiming at their environmental impact and highest activity/selectivity. In this work the best performing catalyst was 1.1wt% of Pd on ZnO which was prepared by washcoating and pre-fabricated Pd NPs. Under optimized conditions with water as solvent 98% of selectivity at 96% conversion was obtained, which was close to the results of the benchmark reaction in batch mode (with 98% selectivity at 99% conversion). Finally, the FFMR demonstrated a 15-fold higher performance in comparison with a batch-operated reactor showing important process intensification for the hydrogenation of (1) to (2) in continuous-flow mode.
doi_str_mv 10.1016/j.cej.2016.02.081
format Article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_1816034784</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>S1385894716301826</els_id><sourcerecordid>1790961713</sourcerecordid><originalsourceid>FETCH-LOGICAL-c400t-afdfa887e33a55a4a0981bb94f4c2047e6e94d994b83966575d242af9011854a3</originalsourceid><addsrcrecordid>eNqFUb1OwzAYjBBIlMIDsHlkSbBjJ7HFhCr-pEosMFuO87k4JHGw00rdeAfekCfBVZhh-PTdcHfS3SXJJcEZwaS8bjMNbZZHmOE8w5wcJQvCK5rSnOTHEVNepFyw6jQ5C6HFGJeCiEXyvnLDZIet24Zuj9wIXk3QIKO6zg4bZGzXo95q7zwoPTmPTLwAHejJ7gC97RvvNjCoyboBOYO08rUbvj-_ZoAmb8cOUIRNOE9Oom-Ai9-_TF7v715Wj-n6-eFpdbtONcN4SpVpjOK8AkpVUSimsOCkrgUzTOeYVVCCYI0QrOZUlGVRFU3OcmUEJoQXTNFlcjX7jt59bCFMsrdBQ9epAWJOSTgpMWUVZ_9TK4FFSSpCI5XM1FhGCB6MHL3tld9LguVhA9nKuIE8bCBxLuMGUXMzayDG3VnwMmgLg4bG-tigbJz9Q_0D-PKRaw</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1790961713</pqid></control><display><type>article</type><title>Continuously operated falling film microreactor for selective hydrogenation of carbon–carbon triple bonds</title><source>Elsevier ScienceDirect Journals Complete</source><creator>Rehm, Thomas H. ; Berguerand, Charline ; Ek, Satu ; Zapf, Ralf ; Löb, Patrick ; Nikoshvili, Linda ; Kiwi-Minsker, Lioubov</creator><creatorcontrib>Rehm, Thomas H. ; Berguerand, Charline ; Ek, Satu ; Zapf, Ralf ; Löb, Patrick ; Nikoshvili, Linda ; Kiwi-Minsker, Lioubov</creatorcontrib><description>[Display omitted] •Process intensification with microstructured reactor equipment.•Continuous-flow gas–liquid–solid reaction.•Novel catalyst development with atomic layer deposition and PVP-Pd NPs.•Water as selectivity-enhancing and environmental friendly solvent. Despite significant advances in the fabrication and applications of microreactors for production of chemicals, their use for catalytic reactions remains a challenge, especially in fine chemical synthesis where the selectivity towards the desired product is an issue. A falling film microstructured reactor (FFMR) was tested in the selective hydrogenation of 2-butyne-1,4-diol (1) to its olefinic derivative (2). The FFMR plates were coated with Al2O3 or ZnO followed by the deposition of Pd nanoparticles (NPs). The oxides were deposited on the microstructured reaction plates using either conventional washcoating or atomic layer deposition (ALD) in the liquid or gas phase, respectively. The Pd-NPs were either formed via impregnation of an organometallic precursor with subsequent reduction, or with pre-fabricated Pd-NPs stabilized in poly(vinyl pyrrolidon) (PVP) with subsequent pyrolysis of the organic matrix and activation in H2 atmosphere. The palladium loading was varied in the range of 1.1–13.6wt%. Different solvents including water, 2-propanol and mixtures with organic bases were tested aiming at their environmental impact and highest activity/selectivity. In this work the best performing catalyst was 1.1wt% of Pd on ZnO which was prepared by washcoating and pre-fabricated Pd NPs. Under optimized conditions with water as solvent 98% of selectivity at 96% conversion was obtained, which was close to the results of the benchmark reaction in batch mode (with 98% selectivity at 99% conversion). Finally, the FFMR demonstrated a 15-fold higher performance in comparison with a batch-operated reactor showing important process intensification for the hydrogenation of (1) to (2) in continuous-flow mode.</description><identifier>ISSN: 1385-8947</identifier><identifier>EISSN: 1873-3212</identifier><identifier>DOI: 10.1016/j.cej.2016.02.081</identifier><language>eng</language><publisher>Elsevier B.V</publisher><subject>Acetylenic alcohol ; Atomic layer deposition ; Catalysts ; Conversion ; C–C triple bond ; Falling film microreactor ; Gas phase modification ; Hydrogenation ; Microreactors ; Nanoparticles ; Palladium ; Palladium nanoparticles ; Selective hydrogenation ; Selectivity</subject><ispartof>Chemical engineering journal (Lausanne, Switzerland : 1996), 2016-06, Vol.293, p.345-354</ispartof><rights>2016 Elsevier B.V.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c400t-afdfa887e33a55a4a0981bb94f4c2047e6e94d994b83966575d242af9011854a3</citedby><cites>FETCH-LOGICAL-c400t-afdfa887e33a55a4a0981bb94f4c2047e6e94d994b83966575d242af9011854a3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.cej.2016.02.081$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,780,784,3550,27924,27925,45995</link.rule.ids></links><search><creatorcontrib>Rehm, Thomas H.</creatorcontrib><creatorcontrib>Berguerand, Charline</creatorcontrib><creatorcontrib>Ek, Satu</creatorcontrib><creatorcontrib>Zapf, Ralf</creatorcontrib><creatorcontrib>Löb, Patrick</creatorcontrib><creatorcontrib>Nikoshvili, Linda</creatorcontrib><creatorcontrib>Kiwi-Minsker, Lioubov</creatorcontrib><title>Continuously operated falling film microreactor for selective hydrogenation of carbon–carbon triple bonds</title><title>Chemical engineering journal (Lausanne, Switzerland : 1996)</title><description>[Display omitted] •Process intensification with microstructured reactor equipment.•Continuous-flow gas–liquid–solid reaction.•Novel catalyst development with atomic layer deposition and PVP-Pd NPs.•Water as selectivity-enhancing and environmental friendly solvent. Despite significant advances in the fabrication and applications of microreactors for production of chemicals, their use for catalytic reactions remains a challenge, especially in fine chemical synthesis where the selectivity towards the desired product is an issue. A falling film microstructured reactor (FFMR) was tested in the selective hydrogenation of 2-butyne-1,4-diol (1) to its olefinic derivative (2). The FFMR plates were coated with Al2O3 or ZnO followed by the deposition of Pd nanoparticles (NPs). The oxides were deposited on the microstructured reaction plates using either conventional washcoating or atomic layer deposition (ALD) in the liquid or gas phase, respectively. The Pd-NPs were either formed via impregnation of an organometallic precursor with subsequent reduction, or with pre-fabricated Pd-NPs stabilized in poly(vinyl pyrrolidon) (PVP) with subsequent pyrolysis of the organic matrix and activation in H2 atmosphere. The palladium loading was varied in the range of 1.1–13.6wt%. Different solvents including water, 2-propanol and mixtures with organic bases were tested aiming at their environmental impact and highest activity/selectivity. In this work the best performing catalyst was 1.1wt% of Pd on ZnO which was prepared by washcoating and pre-fabricated Pd NPs. Under optimized conditions with water as solvent 98% of selectivity at 96% conversion was obtained, which was close to the results of the benchmark reaction in batch mode (with 98% selectivity at 99% conversion). Finally, the FFMR demonstrated a 15-fold higher performance in comparison with a batch-operated reactor showing important process intensification for the hydrogenation of (1) to (2) in continuous-flow mode.</description><subject>Acetylenic alcohol</subject><subject>Atomic layer deposition</subject><subject>Catalysts</subject><subject>Conversion</subject><subject>C–C triple bond</subject><subject>Falling film microreactor</subject><subject>Gas phase modification</subject><subject>Hydrogenation</subject><subject>Microreactors</subject><subject>Nanoparticles</subject><subject>Palladium</subject><subject>Palladium nanoparticles</subject><subject>Selective hydrogenation</subject><subject>Selectivity</subject><issn>1385-8947</issn><issn>1873-3212</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><recordid>eNqFUb1OwzAYjBBIlMIDsHlkSbBjJ7HFhCr-pEosMFuO87k4JHGw00rdeAfekCfBVZhh-PTdcHfS3SXJJcEZwaS8bjMNbZZHmOE8w5wcJQvCK5rSnOTHEVNepFyw6jQ5C6HFGJeCiEXyvnLDZIet24Zuj9wIXk3QIKO6zg4bZGzXo95q7zwoPTmPTLwAHejJ7gC97RvvNjCoyboBOYO08rUbvj-_ZoAmb8cOUIRNOE9Oom-Ai9-_TF7v715Wj-n6-eFpdbtONcN4SpVpjOK8AkpVUSimsOCkrgUzTOeYVVCCYI0QrOZUlGVRFU3OcmUEJoQXTNFlcjX7jt59bCFMsrdBQ9epAWJOSTgpMWUVZ_9TK4FFSSpCI5XM1FhGCB6MHL3tld9LguVhA9nKuIE8bCBxLuMGUXMzayDG3VnwMmgLg4bG-tigbJz9Q_0D-PKRaw</recordid><startdate>20160601</startdate><enddate>20160601</enddate><creator>Rehm, Thomas H.</creator><creator>Berguerand, Charline</creator><creator>Ek, Satu</creator><creator>Zapf, Ralf</creator><creator>Löb, Patrick</creator><creator>Nikoshvili, Linda</creator><creator>Kiwi-Minsker, Lioubov</creator><general>Elsevier B.V</general><scope>AAYXX</scope><scope>CITATION</scope><scope>7ST</scope><scope>C1K</scope><scope>SOI</scope><scope>7QF</scope><scope>7SR</scope><scope>8BQ</scope><scope>8FD</scope><scope>H8D</scope><scope>JG9</scope><scope>L7M</scope></search><sort><creationdate>20160601</creationdate><title>Continuously operated falling film microreactor for selective hydrogenation of carbon–carbon triple bonds</title><author>Rehm, Thomas H. ; Berguerand, Charline ; Ek, Satu ; Zapf, Ralf ; Löb, Patrick ; Nikoshvili, Linda ; Kiwi-Minsker, Lioubov</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c400t-afdfa887e33a55a4a0981bb94f4c2047e6e94d994b83966575d242af9011854a3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><topic>Acetylenic alcohol</topic><topic>Atomic layer deposition</topic><topic>Catalysts</topic><topic>Conversion</topic><topic>C–C triple bond</topic><topic>Falling film microreactor</topic><topic>Gas phase modification</topic><topic>Hydrogenation</topic><topic>Microreactors</topic><topic>Nanoparticles</topic><topic>Palladium</topic><topic>Palladium nanoparticles</topic><topic>Selective hydrogenation</topic><topic>Selectivity</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Rehm, Thomas H.</creatorcontrib><creatorcontrib>Berguerand, Charline</creatorcontrib><creatorcontrib>Ek, Satu</creatorcontrib><creatorcontrib>Zapf, Ralf</creatorcontrib><creatorcontrib>Löb, Patrick</creatorcontrib><creatorcontrib>Nikoshvili, Linda</creatorcontrib><creatorcontrib>Kiwi-Minsker, Lioubov</creatorcontrib><collection>CrossRef</collection><collection>Environment Abstracts</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Environment Abstracts</collection><collection>Aluminium Industry Abstracts</collection><collection>Engineered Materials Abstracts</collection><collection>METADEX</collection><collection>Technology Research Database</collection><collection>Aerospace Database</collection><collection>Materials Research Database</collection><collection>Advanced Technologies Database with Aerospace</collection><jtitle>Chemical engineering journal (Lausanne, Switzerland : 1996)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Rehm, Thomas H.</au><au>Berguerand, Charline</au><au>Ek, Satu</au><au>Zapf, Ralf</au><au>Löb, Patrick</au><au>Nikoshvili, Linda</au><au>Kiwi-Minsker, Lioubov</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Continuously operated falling film microreactor for selective hydrogenation of carbon–carbon triple bonds</atitle><jtitle>Chemical engineering journal (Lausanne, Switzerland : 1996)</jtitle><date>2016-06-01</date><risdate>2016</risdate><volume>293</volume><spage>345</spage><epage>354</epage><pages>345-354</pages><issn>1385-8947</issn><eissn>1873-3212</eissn><abstract>[Display omitted] •Process intensification with microstructured reactor equipment.•Continuous-flow gas–liquid–solid reaction.•Novel catalyst development with atomic layer deposition and PVP-Pd NPs.•Water as selectivity-enhancing and environmental friendly solvent. Despite significant advances in the fabrication and applications of microreactors for production of chemicals, their use for catalytic reactions remains a challenge, especially in fine chemical synthesis where the selectivity towards the desired product is an issue. A falling film microstructured reactor (FFMR) was tested in the selective hydrogenation of 2-butyne-1,4-diol (1) to its olefinic derivative (2). The FFMR plates were coated with Al2O3 or ZnO followed by the deposition of Pd nanoparticles (NPs). The oxides were deposited on the microstructured reaction plates using either conventional washcoating or atomic layer deposition (ALD) in the liquid or gas phase, respectively. The Pd-NPs were either formed via impregnation of an organometallic precursor with subsequent reduction, or with pre-fabricated Pd-NPs stabilized in poly(vinyl pyrrolidon) (PVP) with subsequent pyrolysis of the organic matrix and activation in H2 atmosphere. The palladium loading was varied in the range of 1.1–13.6wt%. Different solvents including water, 2-propanol and mixtures with organic bases were tested aiming at their environmental impact and highest activity/selectivity. In this work the best performing catalyst was 1.1wt% of Pd on ZnO which was prepared by washcoating and pre-fabricated Pd NPs. Under optimized conditions with water as solvent 98% of selectivity at 96% conversion was obtained, which was close to the results of the benchmark reaction in batch mode (with 98% selectivity at 99% conversion). Finally, the FFMR demonstrated a 15-fold higher performance in comparison with a batch-operated reactor showing important process intensification for the hydrogenation of (1) to (2) in continuous-flow mode.</abstract><pub>Elsevier B.V</pub><doi>10.1016/j.cej.2016.02.081</doi><tpages>10</tpages></addata></record>
fulltext fulltext
identifier ISSN: 1385-8947
ispartof Chemical engineering journal (Lausanne, Switzerland : 1996), 2016-06, Vol.293, p.345-354
issn 1385-8947
1873-3212
language eng
recordid cdi_proquest_miscellaneous_1816034784
source Elsevier ScienceDirect Journals Complete
subjects Acetylenic alcohol
Atomic layer deposition
Catalysts
Conversion
C–C triple bond
Falling film microreactor
Gas phase modification
Hydrogenation
Microreactors
Nanoparticles
Palladium
Palladium nanoparticles
Selective hydrogenation
Selectivity
title Continuously operated falling film microreactor for selective hydrogenation of carbon–carbon triple bonds
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-28T04%3A17%3A07IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Continuously%20operated%20falling%20film%20microreactor%20for%20selective%20hydrogenation%20of%20carbon%E2%80%93carbon%20triple%20bonds&rft.jtitle=Chemical%20engineering%20journal%20(Lausanne,%20Switzerland%20:%201996)&rft.au=Rehm,%20Thomas%20H.&rft.date=2016-06-01&rft.volume=293&rft.spage=345&rft.epage=354&rft.pages=345-354&rft.issn=1385-8947&rft.eissn=1873-3212&rft_id=info:doi/10.1016/j.cej.2016.02.081&rft_dat=%3Cproquest_cross%3E1790961713%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=1790961713&rft_id=info:pmid/&rft_els_id=S1385894716301826&rfr_iscdi=true