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Catalytic Conversion of Free Fatty Acids to Bio-Based Aromatics: A Model Investigation Using Oleic Acid and an H-ZSM-5/Al(2)O(3) Catalyst
[Image: see text] The catalytic conversion of oleic acid to aromatics (benzene, toluene, and xylenes, BTX) over a granular H-ZSM-5/Al(2)O(3) catalyst (ϕ 1.2–1.8 mm, 10 g loading) was investigated in a continuous bench-scale fixed-bed reactor (10 g oleic acid h(–1)). A peak carbon yield of aromatics...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American
Chemical Society
2021
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7842136/ https://www.ncbi.nlm.nih.gov/pubmed/33520476 http://dx.doi.org/10.1021/acssuschemeng.0c06181 |
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author | He, Songbo Klein, Frederike Gerda Hiltje Kramer, Thomas Sjouke Chandel, Anshu Tegudeer, Zhuorigebatu Heeres, Andre Heeres, Hero Jan |
author_facet | He, Songbo Klein, Frederike Gerda Hiltje Kramer, Thomas Sjouke Chandel, Anshu Tegudeer, Zhuorigebatu Heeres, Andre Heeres, Hero Jan |
author_sort | He, Songbo |
collection | PubMed |
description | [Image: see text] The catalytic conversion of oleic acid to aromatics (benzene, toluene, and xylenes, BTX) over a granular H-ZSM-5/Al(2)O(3) catalyst (ϕ 1.2–1.8 mm, 10 g loading) was investigated in a continuous bench-scale fixed-bed reactor (10 g oleic acid h(–1)). A peak carbon yield of aromatics of 27.4% was obtained at a catalyst bed temperature of 550 °C and atmospheric pressure. BTX was the major aromatics formed (peak carbon yield was 22.7%), and a total BTX production of 1000 mg g(–1) catalyst was achieved within a catalyst lifetime of 6.5 h for the fresh catalyst. The catalyst was deactivated due to severe coke deposition (ca. 22.1 wt % on the catalyst). The used catalyst was reactivated by an ex situ oxidative regeneration at 680 °C in air for 12 h. The regenerated catalyst was subsequently recycled, and in total, 7 cycles of reaction-regeneration were performed. A gradual decrease in the peak carbon yield of BTX was observed with reaction-regeneration cycles (e.g., to 16.3% for the catalyst regenerated for 6 times). However, the catalyst lifetime was remarkably prolonged (e.g., >24 h), leading to a significantly enhanced total BTX production (e.g., 3000 mg g(–1) catalyst in 24 h). The fresh, used, and regenerated catalysts were characterized by N(2) and Ar physisorption, XRD, HR-TEM-EDX, (27)Al, and (29)Si MAS ssNMR, NH(3)-TPD, TGA, and CHN elemental analysis. Negligible changes in textural properties, crystalline structure, and framework occurred after one reaction-regeneration cycle, except for a slight decrease in acidity. However, dealumination of the H-ZSM-5 framework was observed after 7 cycles of reaction-regeneration, leading to a decrease in microporosity, crystallinity, and acidity. Apparently, these changes are not detrimental for catalyst activity, and actually, the lifetime of the catalyst increases, rationalized by considering that coke formation rates are retarded when the acidity is reduced. |
format | Online Article Text |
id | pubmed-7842136 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | American
Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-78421362021-01-29 Catalytic Conversion of Free Fatty Acids to Bio-Based Aromatics: A Model Investigation Using Oleic Acid and an H-ZSM-5/Al(2)O(3) Catalyst He, Songbo Klein, Frederike Gerda Hiltje Kramer, Thomas Sjouke Chandel, Anshu Tegudeer, Zhuorigebatu Heeres, Andre Heeres, Hero Jan ACS Sustain Chem Eng [Image: see text] The catalytic conversion of oleic acid to aromatics (benzene, toluene, and xylenes, BTX) over a granular H-ZSM-5/Al(2)O(3) catalyst (ϕ 1.2–1.8 mm, 10 g loading) was investigated in a continuous bench-scale fixed-bed reactor (10 g oleic acid h(–1)). A peak carbon yield of aromatics of 27.4% was obtained at a catalyst bed temperature of 550 °C and atmospheric pressure. BTX was the major aromatics formed (peak carbon yield was 22.7%), and a total BTX production of 1000 mg g(–1) catalyst was achieved within a catalyst lifetime of 6.5 h for the fresh catalyst. The catalyst was deactivated due to severe coke deposition (ca. 22.1 wt % on the catalyst). The used catalyst was reactivated by an ex situ oxidative regeneration at 680 °C in air for 12 h. The regenerated catalyst was subsequently recycled, and in total, 7 cycles of reaction-regeneration were performed. A gradual decrease in the peak carbon yield of BTX was observed with reaction-regeneration cycles (e.g., to 16.3% for the catalyst regenerated for 6 times). However, the catalyst lifetime was remarkably prolonged (e.g., >24 h), leading to a significantly enhanced total BTX production (e.g., 3000 mg g(–1) catalyst in 24 h). The fresh, used, and regenerated catalysts were characterized by N(2) and Ar physisorption, XRD, HR-TEM-EDX, (27)Al, and (29)Si MAS ssNMR, NH(3)-TPD, TGA, and CHN elemental analysis. Negligible changes in textural properties, crystalline structure, and framework occurred after one reaction-regeneration cycle, except for a slight decrease in acidity. However, dealumination of the H-ZSM-5 framework was observed after 7 cycles of reaction-regeneration, leading to a decrease in microporosity, crystallinity, and acidity. Apparently, these changes are not detrimental for catalyst activity, and actually, the lifetime of the catalyst increases, rationalized by considering that coke formation rates are retarded when the acidity is reduced. American Chemical Society 2021-01-11 2021-01-25 /pmc/articles/PMC7842136/ /pubmed/33520476 http://dx.doi.org/10.1021/acssuschemeng.0c06181 Text en © 2021 American Chemical Society This is an open access article published under a Creative Commons Non-Commercial No Derivative Works (CC-BY-NC-ND) Attribution License (http://pubs.acs.org/page/policy/authorchoice_ccbyncnd_termsofuse.html) , which permits copying and redistribution of the article, and creation of adaptations, all for non-commercial purposes. |
spellingShingle | He, Songbo Klein, Frederike Gerda Hiltje Kramer, Thomas Sjouke Chandel, Anshu Tegudeer, Zhuorigebatu Heeres, Andre Heeres, Hero Jan Catalytic Conversion of Free Fatty Acids to Bio-Based Aromatics: A Model Investigation Using Oleic Acid and an H-ZSM-5/Al(2)O(3) Catalyst |
title | Catalytic Conversion of Free Fatty Acids to Bio-Based
Aromatics: A Model Investigation Using Oleic Acid and an H-ZSM-5/Al(2)O(3) Catalyst |
title_full | Catalytic Conversion of Free Fatty Acids to Bio-Based
Aromatics: A Model Investigation Using Oleic Acid and an H-ZSM-5/Al(2)O(3) Catalyst |
title_fullStr | Catalytic Conversion of Free Fatty Acids to Bio-Based
Aromatics: A Model Investigation Using Oleic Acid and an H-ZSM-5/Al(2)O(3) Catalyst |
title_full_unstemmed | Catalytic Conversion of Free Fatty Acids to Bio-Based
Aromatics: A Model Investigation Using Oleic Acid and an H-ZSM-5/Al(2)O(3) Catalyst |
title_short | Catalytic Conversion of Free Fatty Acids to Bio-Based
Aromatics: A Model Investigation Using Oleic Acid and an H-ZSM-5/Al(2)O(3) Catalyst |
title_sort | catalytic conversion of free fatty acids to bio-based
aromatics: a model investigation using oleic acid and an h-zsm-5/al(2)o(3) catalyst |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7842136/ https://www.ncbi.nlm.nih.gov/pubmed/33520476 http://dx.doi.org/10.1021/acssuschemeng.0c06181 |
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