Insights into reductive depolymerization of Kraft lignin to produce aromatics in the presence of Pt/HZSM-23 catalyst

Lignin is one of the primary residues obtained after the processing of lignocellulosic biomass. However, most residual lignin is burnt directly to get rid of it, albeit one of the few biorenewable waste resources that can yield aromatics. Therefore, the present study investigates reductive depolymer...

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Autores principales: Akshay R. Mankar, Ejaz Ahmad, Kamal K. Pant
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Publicado: KeAi Communications Co., Ltd. 2021
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spelling oai:doaj.org-article:1ac568add6294195adffcbebc5ff1c742021-11-30T04:17:12ZInsights into reductive depolymerization of Kraft lignin to produce aromatics in the presence of Pt/HZSM-23 catalyst2589-299110.1016/j.mset.2021.08.006https://doaj.org/article/1ac568add6294195adffcbebc5ff1c742021-01-01T00:00:00Zhttp://www.sciencedirect.com/science/article/pii/S2589299121000331https://doaj.org/toc/2589-2991Lignin is one of the primary residues obtained after the processing of lignocellulosic biomass. However, most residual lignin is burnt directly to get rid of it, albeit one of the few biorenewable waste resources that can yield aromatics. Therefore, the present study investigates reductive depolymerization of Kraft lignin into aromatics in the presence of Pt/HZSM-23 catalyst. In this regard, the lignin conversion experiments were performed under mild reaction conditions at a temperature range of 100 °C to 200 °C for 1 h to 12 h in a high-pressure batch reactor. Besides, a comparative study was done on the effect of the supply of external hydrogen and in-situ hydrogenation. Eventually, 87.3% lignin conversion was measured yielding 65.1% bio-oil, primarily aromatics at optimized experimental conditions. It was observed that the mesopores in the Pt/HZSM-23 catalyst facilitate the transfer of larger molecules derived from the Kraft lignin, thus causing an overall improvement in the catalytic activity. A mechanistic study based on experimental conditions and products detected using GC-MS revealed that the in-situ hydrogen transfer route is more favorable for lignin depolymerization than externally supplied hydrogen.Akshay R. MankarEjaz AhmadKamal K. PantKeAi Communications Co., Ltd.articleKraft ligninReductive depolymerizationPhenolsAromaticsBio-oilPt/HZSM-23Materials of engineering and construction. Mechanics of materialsTA401-492Energy conservationTJ163.26-163.5ENMaterials Science for Energy Technologies, Vol 4, Iss , Pp 341-348 (2021)
institution DOAJ
collection DOAJ
language EN
topic Kraft lignin
Reductive depolymerization
Phenols
Aromatics
Bio-oil
Pt/HZSM-23
Materials of engineering and construction. Mechanics of materials
TA401-492
Energy conservation
TJ163.26-163.5
spellingShingle Kraft lignin
Reductive depolymerization
Phenols
Aromatics
Bio-oil
Pt/HZSM-23
Materials of engineering and construction. Mechanics of materials
TA401-492
Energy conservation
TJ163.26-163.5
Akshay R. Mankar
Ejaz Ahmad
Kamal K. Pant
Insights into reductive depolymerization of Kraft lignin to produce aromatics in the presence of Pt/HZSM-23 catalyst
description Lignin is one of the primary residues obtained after the processing of lignocellulosic biomass. However, most residual lignin is burnt directly to get rid of it, albeit one of the few biorenewable waste resources that can yield aromatics. Therefore, the present study investigates reductive depolymerization of Kraft lignin into aromatics in the presence of Pt/HZSM-23 catalyst. In this regard, the lignin conversion experiments were performed under mild reaction conditions at a temperature range of 100 °C to 200 °C for 1 h to 12 h in a high-pressure batch reactor. Besides, a comparative study was done on the effect of the supply of external hydrogen and in-situ hydrogenation. Eventually, 87.3% lignin conversion was measured yielding 65.1% bio-oil, primarily aromatics at optimized experimental conditions. It was observed that the mesopores in the Pt/HZSM-23 catalyst facilitate the transfer of larger molecules derived from the Kraft lignin, thus causing an overall improvement in the catalytic activity. A mechanistic study based on experimental conditions and products detected using GC-MS revealed that the in-situ hydrogen transfer route is more favorable for lignin depolymerization than externally supplied hydrogen.
format article
author Akshay R. Mankar
Ejaz Ahmad
Kamal K. Pant
author_facet Akshay R. Mankar
Ejaz Ahmad
Kamal K. Pant
author_sort Akshay R. Mankar
title Insights into reductive depolymerization of Kraft lignin to produce aromatics in the presence of Pt/HZSM-23 catalyst
title_short Insights into reductive depolymerization of Kraft lignin to produce aromatics in the presence of Pt/HZSM-23 catalyst
title_full Insights into reductive depolymerization of Kraft lignin to produce aromatics in the presence of Pt/HZSM-23 catalyst
title_fullStr Insights into reductive depolymerization of Kraft lignin to produce aromatics in the presence of Pt/HZSM-23 catalyst
title_full_unstemmed Insights into reductive depolymerization of Kraft lignin to produce aromatics in the presence of Pt/HZSM-23 catalyst
title_sort insights into reductive depolymerization of kraft lignin to produce aromatics in the presence of pt/hzsm-23 catalyst
publisher KeAi Communications Co., Ltd.
publishDate 2021
url https://doaj.org/article/1ac568add6294195adffcbebc5ff1c74
work_keys_str_mv AT akshayrmankar insightsintoreductivedepolymerizationofkraftlignintoproducearomaticsinthepresenceofpthzsm23catalyst
AT ejazahmad insightsintoreductivedepolymerizationofkraftlignintoproducearomaticsinthepresenceofpthzsm23catalyst
AT kamalkpant insightsintoreductivedepolymerizationofkraftlignintoproducearomaticsinthepresenceofpthzsm23catalyst
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