胶体三维和二维银纳米颗粒的聚集稳定性,由11-巯基十四酸稳定,在单电荷阳离子存在下

P. Malakhovsky, Alexey V. Rashkevich, E. A. Minakov, M. Artemyev
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引用次数: 0

摘要

在pH 8.0、浓度为0.02 mol/L、含有不同单电荷阳离子(Li+、Na+、K+、Cs+)和三hcl的磷酸盐缓冲液存在下,模拟纳米颗粒与生物分子的碳二亚胺偶联条件,研究了11-巯基十四酸稳定的胶体银准球形纳米颗粒和二维纳米板的聚集稳定性。在na -磷酸缓冲液存在的情况下,银纳米板发生聚集,而在相同条件下,准球形纳米颗粒保持胶体稳定性。三维和二维银纳米颗粒的胶体稳定性差异是由于纳米板基面上的表观酸解离常数的增加以及随后的特定桥接相互作用的增加,这种桥接相互作用可以通过在配体层中引入非离子间隔剂(11-巯基-1-十一醇)来消除。具有混合配体层的银纳米板在不同的pH值范围内提高了胶体稳定性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Aggregative stability of colloidal 3D and 2D silver nanoparticles, stabilised by 11-mercaptoundecanoic acid, in the presence of singly charged cations
We studied the aggregative stability of colloidal silver quasi-spherical nanoparticles and two-dimensional nanoplates, stabilised by 11-mercaptoundecanoic acid, in the presence of phosphate buffers containing different singly charged cations (Li+ , Na+ , K+ , Cs+) and tris-HCl at pH 8.0 and concentration 0.02 mol/L which mimics the carbodiimide conjugation conditions of nanoparticles with biomolecules. Aggregation of silver nanoplates occurs in the presence of Na-phosphate buffer whereas at the same conditions the quasi-spherical nanoparticles retain colloidal stability. The difference in colloidal stability between 3D and 2D silver nanoparticles is due to the increase of the apparent acid dissociation constant on the nanoplates’ basal faces and the subsequent increase in specific bridging interactions nanoparticle – cation – nanoparticle which can be eliminated by introducing of non-ionic spacer (11-mercapto-1-undecanol) in the ligand layer. Silver nanoplates with mixed ligand layer have increased colloidal stability across the pH.
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