分子模拟驱动的功能化纤维素纳米晶体在乙醇中的分散性和稳定性的设计。

IF 3.9 2区 化学 Q2 CHEMISTRY, MULTIDISCIPLINARY
Langmuir Pub Date : 2025-06-17 Epub Date: 2025-06-02 DOI:10.1021/acs.langmuir.5c00312
Arash Elahi, Haoyang You, Stuart J Rowan, Santanu Chaudhuri
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引用次数: 0

摘要

纤维素纳米晶体(cnc)通常具有羧酸表面官能团,因为它有助于在水溶液中的分散。然而,羧酸功能化的cnc (cnc - cooh)由于其自聚集性,在非水溶剂中表现出较差的分散性,限制了它们在许多生物源溶剂基技术中的应用,如喷墨打印、旋转涂层等。为了提高cnc在非水溶剂中的分散性,通过分子动力学模拟研究了cnc - cooh在生物源乙醇中分散性低的潜在原因,并研究了表面功能化如何影响其在非水溶剂中的自聚集倾向。平均力势(PMF)计算表明,cnc - cooh通过亲水性表面聚集导致其在乙醇中的低分散性,而cnc - cooh与烷基(CNC-COOH-alkyl,烷基是乙基、丁基、己基和辛基)的功能化降低了它们的聚集倾向。烷基化的cnc比cnc - cooh的结合倾向更低,这是因为烷基化增加了结合cnc之间的距离,使得它们的结合熵损失更高,表面之间的吸引力更小。cnc - cooh -烷基的高结合熵损失是由于在cnc - cooh -烷基之间的接触点烷基的自由度降低。因此,当cnc - cooh与较长的烷基(即己基和辛基)进行官能团化时,其分散性最高。pmf推导的结合自由能值预测了分散性的趋势为:CNC-COOH-辛基≈CNC-COOH-己基> CNC-COOH-丁基> CNC-COOH-乙基> CNC-COOH。用乙基、丁基和己基合成的CNC- cooh -烷基的实验测试证实了模拟预测,其中烷基链尺寸的增加增加了CNC的分散性。cnc - cooh -己基在乙醇中分散良好,1天内保持稳定。本研究的发现增强了我们对cnc功能化如何提高其在生物源非水溶剂(如乙醇)中的稳定性的理解,并为其在生物源溶剂基技术中的整合开辟了道路。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Molecular Simulation-Driven Design of Functionalized Cellulose Nanocrystals toward Improved Dispersibility and Stabilization in Ethanol.

Molecular Simulation-Driven Design of Functionalized Cellulose Nanocrystals toward Improved Dispersibility and Stabilization in Ethanol.

Cellulose nanocrystals (CNCs) are commonly produced with carboxylic acid surface functionalities, as it aids the dispersion in aqueous solvents. However, the carboxylic acid-functionalized CNCs (CNC-COOHs) exhibit poor dispersibility in nonaqueous solvents due to their self-aggregation, limiting their integration into many biosourced solvent-based technologies, such as inkjet printing, spin-coating, etc. Aimed at improving the dispersibility of CNCs in nonaqueous solvents, molecular dynamics simulations were performed to study the underlying reasons for the low dispersibility of CNC-COOHs in biosourced ethanol and investigate how surface functionalization impacts their self-aggregation tendency in this solvent. The potential of mean force (PMF) calculations revealed that the aggregation of CNC-COOHs through their hydrophilic surfaces drives their low dispersibility in ethanol and that the functionalization of CNC-COOHs with alkyl groups (CNC-COOH-alkyl, with alkyl being ethyl, butyl, hexyl, and octyl) reduces their aggregation tendency. The lower binding tendency of the alkylated CNCs than CNC-COOHs stems from a higher binding entropy loss and a lower attraction between their surfaces, as alkylation increases the distance between bound CNCs. The higher binding entropy loss of CNC-COOH-alkyls is attributed to alkyl groups' reduced degrees of freedom at the contact point between CNC-COOH-alkyls. As a result, the highest dispersibility can be achieved when the CNC-COOHs are functionalized with the longer alkyl groups, i.e., hexyl and octyl. PMF-derived binding free energy values predict the dispersibility trend as CNC-COOH-octyl ≈ CNC-COOH-hexyl > CNC-COOH-butyl > CNC-COOH-ethyl > CNC-COOH. Experimental tests for synthesized CNC-COOH-alkyls with ethyl, butyl, and hexyl groups confirmed simulation predictions, wherein the increasing size of the alkyl chain increased CNC dispersibility. CNC-COOH-hexyl dispersed well in ethanol and remained stable for 1 day. The findings of this research enhanced our understanding of how functionalization of the CNCs improves their stability in biosourced nonaqueous solvents such as ethanol and opens the avenue for their integration in biosourced solvent-based technologies.

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来源期刊
Langmuir
Langmuir 化学-材料科学:综合
CiteScore
6.50
自引率
10.30%
发文量
1464
审稿时长
2.1 months
期刊介绍: Langmuir is an interdisciplinary journal publishing articles in the following subject categories: Colloids: surfactants and self-assembly, dispersions, emulsions, foams Interfaces: adsorption, reactions, films, forces Biological Interfaces: biocolloids, biomolecular and biomimetic materials Materials: nano- and mesostructured materials, polymers, gels, liquid crystals Electrochemistry: interfacial charge transfer, charge transport, electrocatalysis, electrokinetic phenomena, bioelectrochemistry Devices and Applications: sensors, fluidics, patterning, catalysis, photonic crystals However, when high-impact, original work is submitted that does not fit within the above categories, decisions to accept or decline such papers will be based on one criteria: What Would Irving Do? Langmuir ranks #2 in citations out of 136 journals in the category of Physical Chemistry with 113,157 total citations. The journal received an Impact Factor of 4.384*. This journal is also indexed in the categories of Materials Science (ranked #1) and Multidisciplinary Chemistry (ranked #5).
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