Naphthols improve lignin separation and induce photoluminescent structural changes during glycolic acid/pentanol biphasic pretreatment of poplar

IF 10.6 1区 化学 Q1 CHEMISTRY, MULTIDISCIPLINARY
Green Chemistry Pub Date : 2026-06-22 Epub Date: 2026-06-08 DOI:10.1039/d6gc02097f
Hong Liao , Wenjun Ying , Junjun Zhu , Huayou Chen , Junhua Zhang
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引用次数: 0

Abstract

Aromatic naphthol additives offer a scalable way to regulate biphasic pretreatment through phase-selective partitioning, enabling simultaneous lignin valorization into photofunctional lignin and efficient hemicellulose conversion within a single processing step. In a glycolic acid/pentanol system for poplar, partitioning analysis showed that 2-naphthol and 3-hydroxy-2-naphthoic acid were enriched in the pentanol phase. At 20 mM, both additives only mildly influenced aqueous-phase xylan hydrolysis, and xylan to xylooligosaccharides (XOS) selectivity was retained, with XOS yields remaining at 46.2–47.5%. This phase-selective partitioning directed lignin reactions toward arylation-type stabilization pathways, while delignification increased from 75.3% to 88.5–90.3%, surface lignin coverage on the solids decreased by 24%, and glucose yields after enzymatic hydrolysis rose from 79.1% to 90.3–92.6%. NMR spectroscopy showed near-complete loss of β-O-4 linkages (from 56.3% to 1.4–2.4%), attenuation of condensed phenolic structures, and clear naphthalene resonances indicative of naphthol incorporation. The resulting lignin fractions exhibited solvent-tunable autofluorescence, with a quantum yield of up to 14% in tetrahydrofuran, attributable to π-conjugation extension and rigidification that suppress nonradiative decay. This photofunctional lignin holds significant potential for applications in biobased fluorescent coatings. This approach establishes a novel route for the co-production of high-value photofunctional lignin and sugars from lignocellulose, transforming a traditional biorefinery waste stream into a structurally engineered optical material.

Abstract Image

在杨树乙醇酸/戊醇双相预处理过程中,萘酚类物质改善了木质素的分离,诱导了木质素的光致发光结构变化
芳香族萘酚添加剂提供了一种可扩展的方法,通过相选择分配来调节双相预处理,使木质素在单个处理步骤内同时增值为光功能木质素和有效的半纤维素转化。在杨树乙醇酸/戊醇体系中,分配分析表明,戊醇相中富集了2-萘酚和3-羟基-2-萘酸。在20 mM时,两种添加剂对水相木聚糖水解均有轻微影响,木聚糖对低聚木糖(XOS)的选择性保持不变,XOS产率保持在46.2-47.5%。这种相选择性分配将木质素反应导向芳基化型稳定途径,而脱木质素从75.3%增加到88.5-90.3%,固体表面木质素覆盖率降低24%,酶解后的葡萄糖收率从79.1%提高到90.3-92.6%。核磁共振波谱显示,β-O-4键几乎完全丧失(从56.3%降至1.4-2.4%),浓缩酚结构衰减,萘共振清晰,表明萘酚掺入。所得到的木质素组分表现出溶剂可调的自身荧光,在四氢呋喃中的量子产率高达14%,这是由于π共轭延伸和固化抑制了非辐射衰变。这种具有光功能的木质素在生物基荧光涂料中具有重要的应用潜力。这种方法为从木质纤维素中联合生产高价值的光功能木质素和糖建立了一条新途径,将传统的生物炼制废物流转化为结构工程光学材料。
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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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