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One-step fabrication of carbonaceous solid acid derived from lignosulfonate for the synthesis of biobased furan derivatives

An eco-friendly and low-cost lignosulfonate-based acidic carbonaceous catalyst (LS-SO(3)H) was effectively fabricated using the sulfite pulping by-product of sodium lignosulfonate as a precursor by facile one-step simultaneous carbonization and sulfonation, and employed for the synthesis of promisin...

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Autores principales: Yu, Xin, Peng, Lincai, Gao, Xueying, He, Liang, Chen, Keli
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9080275/
https://www.ncbi.nlm.nih.gov/pubmed/35539460
http://dx.doi.org/10.1039/c8ra02056f
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author Yu, Xin
Peng, Lincai
Gao, Xueying
He, Liang
Chen, Keli
author_facet Yu, Xin
Peng, Lincai
Gao, Xueying
He, Liang
Chen, Keli
author_sort Yu, Xin
collection PubMed
description An eco-friendly and low-cost lignosulfonate-based acidic carbonaceous catalyst (LS-SO(3)H) was effectively fabricated using the sulfite pulping by-product of sodium lignosulfonate as a precursor by facile one-step simultaneous carbonization and sulfonation, and employed for the synthesis of promising biofuel furan derivatives from biorenewable feedstocks. The catalyst preparation conditions significantly affected the preparation and properties of LS-SO(3)H. A relatively high catalyst preparation yield (40.4%) with strong –SO(3)H density (1.33 mmol g(−1)) were achieved when the lignosulfonate was treated in concentrated H(2)SO(4) solution at 120 °C for 6 h. The preparation yield of LS-SO(3)H was nearly twice as much as that of one-step prepared catalyst using alkaline lignin (another technical lignin from pulping) as a precursor. The as-prepared LS-SO(3)H had similar textural characteristics to the frequently-used two-step prepared carbonaceous catalyst involving pyrolysis carbonization and sulfonation. LS-SO(3)H was found to show good catalytic activity for the synthesis of 5-ethoxymethylfurfural (EMF) in ethanol medium, affording around 86%, 57% and 47% yields from 5-hydroxymethylfurfural (HMF), fructose and inulin, respectively. Also, a high HMF yield of 83% could be obtained from fructose when DMSO was replaced as reaction medium. The used LS-SO(3)H was readily recovered by filtration, and remained active in recycle runs.
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spelling pubmed-90802752022-05-09 One-step fabrication of carbonaceous solid acid derived from lignosulfonate for the synthesis of biobased furan derivatives Yu, Xin Peng, Lincai Gao, Xueying He, Liang Chen, Keli RSC Adv Chemistry An eco-friendly and low-cost lignosulfonate-based acidic carbonaceous catalyst (LS-SO(3)H) was effectively fabricated using the sulfite pulping by-product of sodium lignosulfonate as a precursor by facile one-step simultaneous carbonization and sulfonation, and employed for the synthesis of promising biofuel furan derivatives from biorenewable feedstocks. The catalyst preparation conditions significantly affected the preparation and properties of LS-SO(3)H. A relatively high catalyst preparation yield (40.4%) with strong –SO(3)H density (1.33 mmol g(−1)) were achieved when the lignosulfonate was treated in concentrated H(2)SO(4) solution at 120 °C for 6 h. The preparation yield of LS-SO(3)H was nearly twice as much as that of one-step prepared catalyst using alkaline lignin (another technical lignin from pulping) as a precursor. The as-prepared LS-SO(3)H had similar textural characteristics to the frequently-used two-step prepared carbonaceous catalyst involving pyrolysis carbonization and sulfonation. LS-SO(3)H was found to show good catalytic activity for the synthesis of 5-ethoxymethylfurfural (EMF) in ethanol medium, affording around 86%, 57% and 47% yields from 5-hydroxymethylfurfural (HMF), fructose and inulin, respectively. Also, a high HMF yield of 83% could be obtained from fructose when DMSO was replaced as reaction medium. The used LS-SO(3)H was readily recovered by filtration, and remained active in recycle runs. The Royal Society of Chemistry 2018-04-26 /pmc/articles/PMC9080275/ /pubmed/35539460 http://dx.doi.org/10.1039/c8ra02056f Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/
spellingShingle Chemistry
Yu, Xin
Peng, Lincai
Gao, Xueying
He, Liang
Chen, Keli
One-step fabrication of carbonaceous solid acid derived from lignosulfonate for the synthesis of biobased furan derivatives
title One-step fabrication of carbonaceous solid acid derived from lignosulfonate for the synthesis of biobased furan derivatives
title_full One-step fabrication of carbonaceous solid acid derived from lignosulfonate for the synthesis of biobased furan derivatives
title_fullStr One-step fabrication of carbonaceous solid acid derived from lignosulfonate for the synthesis of biobased furan derivatives
title_full_unstemmed One-step fabrication of carbonaceous solid acid derived from lignosulfonate for the synthesis of biobased furan derivatives
title_short One-step fabrication of carbonaceous solid acid derived from lignosulfonate for the synthesis of biobased furan derivatives
title_sort one-step fabrication of carbonaceous solid acid derived from lignosulfonate for the synthesis of biobased furan derivatives
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9080275/
https://www.ncbi.nlm.nih.gov/pubmed/35539460
http://dx.doi.org/10.1039/c8ra02056f
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