利用多元醇基深共晶溶剂从天然生物质中分离低色团木质素

IF 9.3 1区 化学 Q1 CHEMISTRY, MULTIDISCIPLINARY
Green Chemistry Pub Date : 2024-07-15 DOI:10.1039/d4gc01824a
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引用次数: 0

摘要

在尝试从木质纤维素生物质或工业木质素中获取浅色木质素时,现有的基于化学或形态改性的方案都存在产量低、成本高以及缺乏所需规模的可用性等问题。在这项研究中,我们采用基于多羟基乙醇的深共晶溶剂(PA-DES)直接从天然生物质中提取浅色木质素,这种木质素甚至比原生纤维素酶木质素(CEL)更白。分离出的木质素具有较高的回收率(97.36%)、规则的微球状形态、富含 58/100Ar 的 β-醚键、较低的酚羟基含量(1.25 mmol g-1)、极少的羰基含量(0.70 mmol g-1)以及较少的缩合结构,因此产生的发色团含量较低。这种木质素具有出色的防晒效果,只需添加 5 wt%,就能将商用防晒霜的 SPF 值从 15 提高到 40。这项研究为扩大浅色木质素的生产规模和获得近乎完全可消化的纤维素以进一步糖化提供了重要指导。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Low-chromophore lignin isolation from natural biomass with polyol-based deep eutectic solvents†

Low-chromophore lignin isolation from natural biomass with polyol-based deep eutectic solvents†

Low-chromophore lignin isolation from natural biomass with polyol-based deep eutectic solvents†

When attempting to obtain light-color lignin from lignocellulosic biomass or industrial lignin, the available options based on chemical or morphological modification suffer from low yield, high cost, and lack of availability at the required scales. In this study, we adopted a polyhydric-alcohol-based deep eutectic solvent (PA-DES) to directly extract light-color lignin from natural biomass, which is even whiter than native cellulolytic enzyme lignin (CEL). The isolated lignin possessed a high recovery yield (97.36%), regular micro-spherical morphology, enriched β-ether linkage of 58/100Ar, low phenolic hydroxyl content of 1.25 mmol g−1, minimal carbonyl content of 0.70 mmol g−1, and less condensed structures, thus yielding a lower content of chromophores. This lignin showed excellent sunscreen effects, which could enhance the SPF of a commercial sunscreen from 15 to 40 with only 5 wt% addition. This study can provide essential guidance for the scale-up production of light-color lignin and obtaining near-complete digestible cellulose for further saccharification.

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来源期刊
Green Chemistry
Green Chemistry 化学-化学综合
CiteScore
16.10
自引率
7.10%
发文量
677
审稿时长
1.4 months
期刊介绍: Green Chemistry is a journal that provides a unique forum for the publication of innovative research on the development of alternative green and sustainable technologies. The scope of Green Chemistry is based on the definition proposed by Anastas and Warner (Green Chemistry: Theory and Practice, P T Anastas and J C Warner, Oxford University Press, Oxford, 1998), which defines green chemistry as the utilisation of a set of principles that reduces or eliminates the use or generation of hazardous substances in the design, manufacture and application of chemical products. Green Chemistry aims to reduce the environmental impact of the chemical enterprise by developing a technology base that is inherently non-toxic to living things and the environment. The journal welcomes submissions on all aspects of research relating to this endeavor and publishes original and significant cutting-edge research that is likely to be of wide general appeal. For a work to be published, it must present a significant advance in green chemistry, including a comparison with existing methods and a demonstration of advantages over those methods.
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