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在环境条件下使用过氧化氢对软木和硬木硫酸盐木质素进行解聚/氧化的可持续工艺。

Sustainable Process for the Depolymerization/Oxidation of Softwood and Hardwood Kraft Lignins Using Hydrogen Peroxide under Ambient Conditions.

机构信息

Institute for Chemicals and Fuels from Alternative Resources (ICFAR), Western University, London, ON N6A 5B9, Canada.

FPInnovations, 570 boul. Saint-Jean, Pointe-Claire, QC H9R 3J9, Canada.

出版信息

Molecules. 2020 May 16;25(10):2329. doi: 10.3390/molecules25102329.

Abstract

The present study demonstrated a sustainable and cost-effective approach to depolymerize/oxidize softwood (SW) and hardwood (HW) kraft lignins using concentrated hydrogen peroxide at temperatures ranging from 25 to 35 °C, in the absence of catalysts or organic solvents. The degree of lignin depolymerization could be simply controlled by reaction time, and no further separation process was needed at the completion of the treatment. The obtained depolymerized lignin products were comprehensively characterized by GPC-UV, FTIR, P-NMR, TGA, Py-GC/MS and elemental analysis. The weight-average molecular weights (M) of the depolymerized lignins obtained from SW or HW lignin at a lignin/HO mass ratio of 1:1 after treatment for 120 h at room temperature (≈25 °C) were approximately 1420 Da. The contents of carboxylic acid groups in the obtained depolymerized lignins were found to significantly increase compared with those of the untreated raw lignins. Moreover, the depolymerized lignin products had lower thermal decomposition temperatures than those of the raw lignins, as expected, owing to the greatly reduced M. These findings represent a novel solution to lignin depolymerization for the production of chemicals that can be utilized as a bio-substitute for petroleum-based polyols in polyurethane production.

摘要

本研究展示了一种可持续且经济有效的方法,可在 25 至 35°C 的温度范围内,在无催化剂和有机溶剂的情况下,使用浓过氧化氢将软木(SW)和硬木(HW)木质素解聚/氧化。木质素的解聚程度可以通过反应时间来简单控制,并且在处理完成后不需要进一步的分离过程。通过 GPC-UV、FTIR、P-NMR、TGA、Py-GC/MS 和元素分析对获得的解聚木质素产物进行了全面表征。在室温(≈25°C)下处理 120 小时后,木质素/HO 质量比为 1:1 时,从 SW 或 HW 木质素获得的解聚木质素的重均分子量(M)约为 1420 Da。与未经处理的原始木质素相比,获得的解聚木质素中的羧酸基团含量显著增加。此外,由于 M 大大降低,解聚木质素产物的热分解温度低于原始木质素,这是预期的结果。这些发现为木质素解聚生产化学品提供了一种新的解决方案,可作为石油基多元醇的生物替代品用于聚氨酯生产。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/178a/7287583/4eb75c6e3d19/molecules-25-02329-g001.jpg

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