Nucleation as a rate-determining step in catalytic gas generation reactions from liquid phase systems
The observable reaction rate of heterogeneously catalyzed reactions is known to be limited either by the intrinsic kinetics of the catalytic transformation or by the rate of pore and/or film diffusion. Here, we show that in gas generation reactions from liquid reactants, the nucleation of gas bubble...
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Veröffentlicht in: | Science advances 2022-11, Vol.8 (46), p.eade3262-eade3262 |
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creator | Solymosi, Thomas Geißelbrecht, Michael Mayer, Sophie Auer, Michael Leicht, Peter Terlinden, Markus Malgaretti, Paolo Bösmann, Andreas Preuster, Patrick Harting, Jens Thommes, Matthias Vogel, Nicolas Wasserscheid, Peter |
description | The observable reaction rate of heterogeneously catalyzed reactions is known to be limited either by the intrinsic kinetics of the catalytic transformation or by the rate of pore and/or film diffusion. Here, we show that in gas generation reactions from liquid reactants, the nucleation of gas bubbles in the catalyst pore structure represents an additional important rate-limiting step. This is highlighted for the example of catalytic hydrogen release from the liquid organic hydrogen carrier compound perhydro-dibenzyltoluene. A nucleation-inhibited catalytic system produces only dissolved hydrogen with fast saturation of the fluid phase around the active site, while bubble formation enhances mass transfer by more than a factor of 50 in an oscillating reaction regime. Nucleation can be efficiently triggered not only by temperature changes and catalyst surface modification but also by a mechanical stimulus. Our work sheds new light on performance-limiting factors in reactions that are of highest relevance for the future green hydrogen economy. |
doi_str_mv | 10.1126/sciadv.ade3262 |
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Here, we show that in gas generation reactions from liquid reactants, the nucleation of gas bubbles in the catalyst pore structure represents an additional important rate-limiting step. This is highlighted for the example of catalytic hydrogen release from the liquid organic hydrogen carrier compound perhydro-dibenzyltoluene. A nucleation-inhibited catalytic system produces only dissolved hydrogen with fast saturation of the fluid phase around the active site, while bubble formation enhances mass transfer by more than a factor of 50 in an oscillating reaction regime. Nucleation can be efficiently triggered not only by temperature changes and catalyst surface modification but also by a mechanical stimulus. Our work sheds new light on performance-limiting factors in reactions that are of highest relevance for the future green hydrogen economy.</description><identifier>ISSN: 2375-2548</identifier><identifier>EISSN: 2375-2548</identifier><identifier>DOI: 10.1126/sciadv.ade3262</identifier><identifier>PMID: 36383668</identifier><language>eng</language><publisher>United States: American Association for the Advancement of Science</publisher><subject>Chemistry ; Physical and Materials Sciences ; SciAdv r-articles</subject><ispartof>Science advances, 2022-11, Vol.8 (46), p.eade3262-eade3262</ispartof><rights>Copyright © 2022 The Authors, some rights reserved; exclusive licensee American Association for the Advancement of Science. No claim to original U.S. Government Works. Distributed under a Creative Commons Attribution License 4.0 (CC BY). 2022 The Authors</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c390t-39e436b3008c762ccd7aa7f13b3d3ce12650854d8869540a19eca9d7b95ecc0f3</citedby><cites>FETCH-LOGICAL-c390t-39e436b3008c762ccd7aa7f13b3d3ce12650854d8869540a19eca9d7b95ecc0f3</cites><orcidid>0000-0002-0619-6708 ; 0000-0002-1201-451X ; 0000-0002-0474-0845 ; 0000-0002-3702-4976 ; 0000-0002-9831-6905 ; 0000-0003-0053-6545 ; 0000-0001-5947-5017 ; 0000-0003-0864-2617 ; 0000-0001-7502-868X ; 0000-0001-6564-3945 ; 0000-0003-0413-9539 ; 0000-0002-9200-6623 ; 0000-0001-5045-2927</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC9668311/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC9668311/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,860,881,27903,27904,53769,53771</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/36383668$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Solymosi, Thomas</creatorcontrib><creatorcontrib>Geißelbrecht, Michael</creatorcontrib><creatorcontrib>Mayer, Sophie</creatorcontrib><creatorcontrib>Auer, Michael</creatorcontrib><creatorcontrib>Leicht, Peter</creatorcontrib><creatorcontrib>Terlinden, Markus</creatorcontrib><creatorcontrib>Malgaretti, Paolo</creatorcontrib><creatorcontrib>Bösmann, Andreas</creatorcontrib><creatorcontrib>Preuster, Patrick</creatorcontrib><creatorcontrib>Harting, Jens</creatorcontrib><creatorcontrib>Thommes, Matthias</creatorcontrib><creatorcontrib>Vogel, Nicolas</creatorcontrib><creatorcontrib>Wasserscheid, Peter</creatorcontrib><title>Nucleation as a rate-determining step in catalytic gas generation reactions from liquid phase systems</title><title>Science advances</title><addtitle>Sci Adv</addtitle><description>The observable reaction rate of heterogeneously catalyzed reactions is known to be limited either by the intrinsic kinetics of the catalytic transformation or by the rate of pore and/or film diffusion. 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subjects | Chemistry Physical and Materials Sciences SciAdv r-articles |
title | Nucleation as a rate-determining step in catalytic gas generation reactions from liquid phase systems |
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