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利用纳米纤维素胶体探针和分子动力学模拟评价纳米纤维素与水污染物的相互作用。

Evaluation of nanocellulose interaction with water pollutants using nanocellulose colloidal probes and molecular dynamic simulations.

机构信息

Department of Materials and Environmental Chemistry, Stockholm University, 10691 Stockholm, Sweden.

CNR-ICCOM - Institute of Chemistry of Organometallic Compounds, via Moruzzi 1, 56124 Pisa, Italy.

出版信息

Carbohydr Polym. 2020 Feb 1;229:115510. doi: 10.1016/j.carbpol.2019.115510. Epub 2019 Oct 22.

Abstract

Atomic Force Microscope (AFM) probes were successfully functionalized with two types of nanocellulose, namely 2,2,6,6-tetramethylpiperidine-1-oxylradical (TEMPO)-mediated oxidized cellulose nanofibers (TOCNF) and cellulose nanocrystals (CNC) and used to study interfacial interactions of nanocellulose with Cu(II) ions and the Victoria blue B dye in liquid medium. TOCNF modified tip showed higher adhesion force due to adsorption of Cu(II) ions and dye molecules compared to CNC ones. Exploring the adsorption properties through classical reactive molecular dynamics simulations (ReaxFF) at the atomic scale confirmed that the Cu(II) ions promptly migrated and adsorbed onto the nanocelluloses through the co-operative chelating action of carboxyl and hydroxyl species. The adsorbed Cu(II) ions showed the tendency to self-organize by forming nano-clusters of variable size, whereas the dye adopted a flat orientation to maximize its adsorption. The satisfactory agreement between the two techniques suggests that functionalized AFM probes can be successfully used to study nanocellulose surface interactions in dry or aqueous environment.

摘要

原子力显微镜(AFM)探针成功地用两种类型的纳米纤维素功能化,即 2,2,6,6-四甲基哌啶-1-氧基自由基(TEMPO)介导的氧化纤维素纳米纤维(TOCNF)和纤维素纳米晶体(CNC),并用于研究纳米纤维素与 Cu(II)离子和维多利亚蓝 B 染料在液相中的界面相互作用。与 CNC 相比,修饰后的 TOCNF 修饰尖端由于 Cu(II)离子和染料分子的吸附表现出更高的粘附力。通过原子尺度的经典反应分子动力学模拟(ReaxFF)探索吸附性质,证实 Cu(II)离子通过羧基和羟基的协同螯合作用迅速迁移并吸附到纳米纤维素上。吸附的 Cu(II)离子表现出通过形成不同大小的纳米簇自组织的趋势,而染料则采用平面取向以最大化其吸附。两种技术之间的良好一致性表明,功能化的 AFM 探针可成功用于研究干燥或水相环境中的纳米纤维素表面相互作用。

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