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不同烷基链长度的改性二氧化硅纳米颗粒在正辛烷/水界面的界面流变学研究

Interfacial Rheological Investigation of Modified Silica Nanoparticles with Different Alkyl Chain Lengths at the n-Octane/Water Interface.

作者信息

Xu Long, Wen Shijie, Xie Qiuyu, Fan Fangning, Wang Qiang, Zhang Xuehao, Lv Kaihe, Jia Han, Sun Hai

机构信息

Shandong Key Laboratory of Oilfield Chemistry, School of Petroleum Engineering, China University of Petroleum (East China), Qingdao 266580, China.

Key Laboratory of Unconventional Oil & Gas Development, China University of Petroleum (East China), Ministry of Education, Qingdao 266580, China.

出版信息

Molecules. 2024 Aug 7;29(16):3749. doi: 10.3390/molecules29163749.

DOI:10.3390/molecules29163749
PMID:39202828
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11357125/
Abstract

The interfacial dilational rheology of silica nanoparticles (NPs) directly reflects the relationship between surface structure and interfacial behaviors in NPs, which has attracted significant attention in various industrial fields. In this work, modified silica nanoparticles (MNPs) with various alkyl chain lengths were synthesized and systematically characterized using Fourier transform infrared spectra, Zeta potential, and water contact angle measurements. It was found that the MNPs were successfully fabricated with similar degrees of modification. Subsequently, the interfacial behaviors of the MNPs in an n-octane/water system were investigated through interfacial dilational rheological experiments. The length of the modified alkyl chain dominated the hydrophilic-lipophile balance and the interfacial activity of the MNPs, evaluated by the equilibrium interfacial tension (IFT) variation and dilational elasticity modulus. In the large amplitude compression experiment, the balance between the electrostatic repulsion and interfacial activity in the MNPs was responsible for their ordered interfacial arrangement. The MNPs with the hexyl alkyl chain (M6C) presented the optimal amphipathy and could partly overcome the repulsion, causing a dramatic change in surface pressure. This was further confirmed by the variations in IFT and dilational elasticity during the compression path. The study provides novel insights into the interfacial rheology and interactions of functionally modified NPs.

摘要

二氧化硅纳米颗粒(NPs)的界面拉伸流变学直接反映了纳米颗粒表面结构与界面行为之间的关系,这在各个工业领域引起了广泛关注。在这项工作中,合成了具有不同烷基链长度的改性二氧化硅纳米颗粒(MNPs),并使用傅里叶变换红外光谱、Zeta电位和水接触角测量对其进行了系统表征。结果发现,成功制备了具有相似改性程度的MNPs。随后,通过界面拉伸流变学实验研究了MNPs在正辛烷/水体系中的界面行为。通过平衡界面张力(IFT)变化和拉伸弹性模量评估,改性烷基链的长度主导了MNPs的亲水亲油平衡和界面活性。在大振幅压缩实验中,MNPs中静电排斥和界面活性之间的平衡导致了它们有序的界面排列。具有己基烷基链的MNPs(M6C)表现出最佳的两亲性,能够部分克服排斥力,导致表面压力发生显著变化。压缩过程中IFT和拉伸弹性的变化进一步证实了这一点。该研究为功能改性纳米颗粒的界面流变学和相互作用提供了新的见解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7994/11357125/6f57ddec20ea/molecules-29-03749-g009.jpg
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