首页|期刊导航|林业工程学报|低共熔溶剂预处理毛竹制备无醛木材胶黏剂和可发酵糖试验

低共熔溶剂预处理毛竹制备无醛木材胶黏剂和可发酵糖试验OA

Preparation of formaldehyde-free wood adhesive and fermentable sugar from bamboo via deep eutectic solvent pretreatment

中文摘要英文摘要

以毛竹为原料,采用氯化胆碱(ChCl)、草酸(OA)和 1,4-丁二醇(BDO)组成的三元低共熔溶剂(DES)体系进行预处理,旨在高效分离木质素,保持其低缩聚状态并提高物料的可及度,同时探索低缩聚木质素作为环保胶合板胶黏剂的可行性.在经过预处理后,对回收木质素和物料进行凝胶渗透色谱(GPC)、X 射线衍射(XRD)和核磁共振(NMR)等方法分析,探究新型三元体系对原料组分结构的影响与作用机理.结果表明,在 110℃条件下预处理4 h,木质素脱除率可达66.9%,纤维素和木聚糖回收率分别为92.1%和7.5%;酶解后葡萄糖和木糖得率均可达 100%.回收木质素的芳基醚键含量高达 32.6/100Ar,缩聚比例仅为 19.54/100Ar;作为无醛木质素胶黏剂制备胶合板的干、湿胶合强度分别为 1.59 和 1.43 MPa,远超国家标准.同时,经 DES 循环预处理 4 次后仍可保持60%以上的木质素脱除率及85.25%的酶解糖化得率.本研究为探索竹材的拆解以及高值化利用提供了绿色高效的预处理策略,并为生物基无醛胶黏剂的开发奠定了技术基础.

In this study,bamboo was used as raw material and pretreated with a ternary deep eutectic solvent(DES)system consisting of choline chloride(ChCl),oxalic acid(OA),and 1,4-butanediol(BDO).This innovative pretreatment approach was designed not only to efficiently fractionate the main components of lignocellulose but also to preserve the native structural features of lignin.The objective was to achieve effective lignin separation while maintaining a low degree of polycondensation,thereby enhancing substrate accessibility and evaluating the feasibility of utilizing low-polycondensation lignin as an environmentally friendly plywood adhesive.The rationale behind selecting this specific ternary combination lies in the synergistic effects among the constituents:ChCl acts as an effective hydrogen bond acceptor,OA serves as an acidic catalyst for cleaving ether bonds,and BDO enhances solubility and mass transfer during pretreatment.After pretreatment,the obtained samples were subjected to the gel permeation chromatography(GPC),X-ray diffraction(XRD),and nuclear magnetic resonance(NMR)methods for comprehensive structural elucidation.These advanced analytical techniques were employed to explore the influence and interaction mechanism of the ternary DES on the structure of raw material.The results showed that the lignin removal rate could reach 66.9%under 110℃pretreatment for 4 h,and the cellulose and xylan recovery rates were maintained at 92.1%and 7.5%,respectively.Such high delignification efficiency alongside high carbohydrate retention underscores the selectivity of the solvent system.The glucose and xylose yielded after enzymatic hydrolysis could reach 100%,indicating significantly enhanced digestibility of the pretreated biomass.Structural analysis revealed that the aryl ether bond(β-O-4)content of the recovered lignin was as high as 32.6/100Ar,and the polycondensation reaction maintained as low as 19.54/100Ar.This high retention of native linkages is crucial for the subsequent adhesive application,as it improves the reactivity and binding capability of lignin.The dry and wet bonding strengths of the recovered lignin as a plywood adhesive reached 1.59 and 1.43 MPa,respectively,far exceeding the national standard.Moreover,the reusability of the DES system was evaluated to assess its economic and environmental feasibility.At the same time,DES can still maintain a lignin removal rate of more than 60%and a saccharification efficiency of 85.25%after being recycled 4 times.This demonstrates remarkable recyclability,reducing both operational costs and environmental impact.Therefore,this study presents a green and efficient pretreatment strategy for the high-value utilization of lignocellulose and establishes a technical foundation for the development of bio-based adhesives.The results underscore the potential of ternary DESs in biorefinery applications and pave the way for sustainable adhesive production from renewable resources.

张少杰;费宇彬;周雪莲;黄晨;黄曹兴;詹云妮

南京林业大学化学工程学院,江苏省林业资源高效加工利用协同创新中心,南京 210037南京林业大学化学工程学院,江苏省林业资源高效加工利用协同创新中心,南京 210037中国林业科学研究院林产化学工业研究所,江苏省生物质能源与材料重点实验室,南京 210042中国林业科学研究院林产化学工业研究所,江苏省生物质能源与材料重点实验室,南京 210042南京林业大学化学工程学院,江苏省林业资源高效加工利用协同创新中心,南京 210037中国林业科学研究院林产化学工业研究所,江苏省生物质能源与材料重点实验室,南京 210042

低共熔溶剂预处理酶水解木质素阻聚木材胶黏剂

deep eutectic solventpretreatmentenzymatic hydrolysislignin protectionwood adhesive

《林业工程学报》 2026 (3)

109-117,9

国家重点研发计划(2023YFD2201904).

10.13360/j.issn.2096-1359.202504017

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