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工业硫酸盐木质素的工程化:酯化方法在木质素纳米颗粒自组装中的作用。

Engineering of Industrial Kraft Lignin: The Role of Esterification Methods in Lignin Nanoparticle Self-Assembly.

作者信息

Xu Taoran, Riazanova Anastasia V, Lindén Pär A, Henriksson Gunnar, Söderberg L Daniel, Gordobil Oihana, Sevastyanova Olena

机构信息

Wallenberg Wood Science Center, Department of Fiber and Polymer Technology, KTH Royal Institute of Technology, School of Chemistry, Biotechnology and Health, Teknikringen 56, Stockholm, 100 44, Sweden.

Department of Fiber and Polymer Technology, School of Chemistry, Biotechnology and Health, Teknikringen 56, Stockholm, 100 44, Sweden.

出版信息

Biomacromolecules. 2025 Sep 8;26(9):5727-5739. doi: 10.1021/acs.biomac.5c00507. Epub 2025 Aug 18.

Abstract

Lignin nanoparticles (LNPs) are gaining increasing interest for applications in various fields, where the particle homogeneity, morphology, and surface properties are critical for performance. In this study, lignin obtained via kraft process from spruce and eucalyptus was employed as precursor for the fabrication of lignin nanoparticles with tunable physicochemical properties. Linear ester groups with varying chain lengths were introduced to systematically investigate the effects of the hydrophobic moiety distribution on lignin nanoparticle formation via solvent-shifting self-assembly. Results demonstrated that esterification-induced structural changes altered the balance of key noncovalent interactions (hydrogen bonding, π-π stacking, and hydrophobic interactions), which collectively governed the self-assembly process, with longer ester chains promoting compact particles with hydrophobic surfaces. By directly linking molecular-level modification of lignin to alterations in the inter- and intramolecular interactions driving the self-assembly of nanoparticles, this study provides a mechanistic framework for the rational design of lignin nanoparticles through controlled chemical modification, thereby expanding their application flexibility.

摘要

木质素纳米颗粒(LNPs)在各个领域的应用中越来越受到关注,在这些领域中,颗粒的均匀性、形态和表面性质对性能至关重要。在本研究中,通过硫酸盐法从云杉和桉木中获得的木质素被用作制备具有可调物理化学性质的木质素纳米颗粒的前体。引入了具有不同链长的线性酯基,以系统地研究疏水部分分布对通过溶剂转移自组装形成木质素纳米颗粒的影响。结果表明,酯化诱导的结构变化改变了关键非共价相互作用(氢键、π-π堆积和疏水相互作用)的平衡,这些相互作用共同控制了自组装过程,较长的酯链促进了具有疏水表面的致密颗粒的形成。通过将木质素的分子水平修饰直接与驱动纳米颗粒自组装的分子间和分子内相互作用的改变联系起来,本研究为通过可控化学修饰合理设计木质素纳米颗粒提供了一个机制框架,从而扩大了它们的应用灵活性。

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