In Situ Lignin Modification Enabling Enhanced Interfibrillar Interactions in Lignocellulosic Nanomaterials toward Structural Applications

被引:15
作者
Jiang, Shan [1 ]
Liu, Xiuyu [2 ,3 ,4 ]
Wang, Zehai [1 ]
Zhou, Lin [1 ]
Meng, Zhiqian [1 ]
Wang, Xinyi [1 ]
Chen, Guoning [3 ]
Wang, Shuangfei [1 ]
Jiang, Yan [1 ,3 ]
机构
[1] Guangxi Univ, Coll Light Ind & Food Engn, Nanning 530004, Peoples R China
[2] Guangxi Minzu Univ, Sch Chem & Chem Engn, Nanning 530006, Peoples R China
[3] Guangxi Bossco Environm Protect Technol Co Ltd, Nanning 530007, Peoples R China
[4] Guangxi Key Lab Chem & Engn Forest Prod, Nanning 530006, Peoples R China
基金
中国国家自然科学基金;
关键词
lignocellulose nanofibril; in situ modulation; microstructure; hydrogen bond; mechanical performance; structural material; TEMPO-MEDIATED OXIDATION; REACTIVE FORCE-FIELD; CELLULOSE NANOFIBRIL; RESIDUAL LIGNIN; OZONE TREATMENT; HIGH-STRENGTH; DEGRADATION; REAXFF; FIBER; TOUGH;
D O I
10.1021/acssuschemeng.2c07748
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Lignocellulose nanopaper (LNP) assembled from lignocellulose nanofibrils (LCNFs) is an emerging eco-friendly structural material applicable to a variety of fields. Lignin serves as a crucial functional component in the LNP matrix; however, it negatively affects the interfacial hydrogen-bonding behaviors among LCNFs and consequently the inferior mechanical performance of LNP. In this study, a mild ozone-oxidation strategy was used to modify lignin macromolecules in situ without significant degradation of carbohydrate polymers (i.e., cellulose and hemicellulose) in LCNFs whereupon the interfacial hydrogen-bond energy was dramatically improved in the assembly and deformation process of LNP as validated by molecular dynamics simulation. Consequently, the lignin-modified LNP exhibited significantly enhanced tensile strength (from 83 to 140 MPa) and toughness (from 1.9 to 7.1 J/m3), which even surpassed those of conventional cellulose nanopaper. Benefiting from the well-preserved lignocellulosic structure, lignin-modified LNP maintained its inherent favorable water and thermal stability and intriguing optical performance, which supported our developed LNP to be a multifunctional structural material for diversified fields, for example, flexible electronic applications. Additionally, the estimated production cost for our developed LNP was approximately half of that for conventional cellulose nanopaper due to its significantly lower resource inputs such as the material, water, and energy. Overall, our study provides a site-specific macromolecular modulation strategy for the economically and environmentally feasible fabrication of highperformance lignocellulosic nanomaterials toward advanced structural applications.
引用
收藏
页码:7705 / 7718
页数:14
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