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由木质素磺酸盐一步法制备用于合成生物基呋喃衍生物的碳质固体酸。

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

作者信息

Yu Xin, Peng Lincai, Gao Xueying, He Liang, Chen Keli

机构信息

Faculty of Chemical Engineering, Kunming University of Science and Technology Kunming 650500 PR China

出版信息

RSC Adv. 2018 Apr 26;8(28):15762-15772. doi: 10.1039/c8ra02056f. eCollection 2018 Apr 23.

DOI:10.1039/c8ra02056f
PMID:35539460
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9080275/
Abstract

An eco-friendly and low-cost lignosulfonate-based acidic carbonaceous catalyst (LS-SOH) 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-SOH. A relatively high catalyst preparation yield (40.4%) with strong -SOH density (1.33 mmol g) were achieved when the lignosulfonate was treated in concentrated HSO solution at 120 °C for 6 h. The preparation yield of LS-SOH 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-SOH had similar textural characteristics to the frequently-used two-step prepared carbonaceous catalyst involving pyrolysis carbonization and sulfonation. LS-SOH 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-SOH was readily recovered by filtration, and remained active in recycle runs.

摘要

以木质素磺酸钠的亚硫酸盐制浆副产物为前驱体,通过简便的一步碳化磺化法,有效制备了一种环境友好且低成本的木质素磺酸盐基酸性碳质催化剂(LS-SOH),并将其用于从生物可再生原料合成有前景的生物燃料呋喃衍生物。催化剂的制备条件对LS-SOH的制备及性能有显著影响。当木质素磺酸盐在浓硫酸溶液中于120℃处理6小时时,可获得相对较高的催化剂制备产率(40.4%)和较高的-SOH密度(1.33 mmol g)。LS-SOH的制备产率几乎是使用碱性木质素(制浆过程中的另一种工业木质素)作为前驱体一步制备的催化剂的两倍。所制备的LS-SOH具有与常用的两步法制备的碳质催化剂(涉及热解碳化和磺化)相似的结构特征。研究发现,LS-SOH在乙醇介质中对合成5-乙氧基甲基糠醛(EMF)具有良好的催化活性,由5-羟甲基糠醛(HMF)、果糖和菊粉分别得到的产率约为86%、57%和47%。此外,当用二甲基亚砜替代反应介质时,由果糖可获得83%的高HMF产率。使用过的LS-SOH通过过滤易于回收,并在循环使用中保持活性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a8c5/9080275/0dec6821d169/c8ra02056f-f7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a8c5/9080275/81e395d36e5f/c8ra02056f-f1.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a8c5/9080275/25938c2e0380/c8ra02056f-f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a8c5/9080275/edf638d81dae/c8ra02056f-f5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a8c5/9080275/293629699033/c8ra02056f-f6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a8c5/9080275/0dec6821d169/c8ra02056f-f7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a8c5/9080275/81e395d36e5f/c8ra02056f-f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a8c5/9080275/7fd08922e637/c8ra02056f-f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a8c5/9080275/dec019d70866/c8ra02056f-f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a8c5/9080275/25938c2e0380/c8ra02056f-f4.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a8c5/9080275/293629699033/c8ra02056f-f6.jpg
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