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Interfacial Activity of Gold Nanoparticles Coatedwith a Polymeric Patchy Shell and the Role of Spreading Agents

机译:金纳米颗粒包覆的界面活性高分子补丁壳和铺展剂的作用

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摘要

Gold patchy nanoparticles (PPs) were prepared under surfactant-free conditions by functionalization with a binary ligand mixture of polystyrene and poly(ethylene glycol) (PEG) as hydrophobic and hydrophilic ligands, respectively. The interfacial activity of PPs was compared to that of homogeneous hydrophilic nanoparticles (HPs), fully functionalized with PEG, by means of pendant drop tensiometry at water/air and water/decane interfaces. We compared interfacial activities in three different spreading agents: water, water/chloroform, and pure chloroform. We found that the interfacial activity of PPs was close to zero (∼2 mN/m) when the spreading agent was water and increased to ∼14 mN/m when the spreading agent was water/chloroform. When the nanoparticles were deposited with pure chloroform, the interfacial activity reached up to 60 mN/m by compression. In all cases, PPs exhibited higher interfacial activity than HPs, which were not interfacially active, regardless of the spreading agent. The interfacial activity at the water/decane interface was found to be significantly lower than that at the water/airinterface because PPs aggregate in decane. Interfacial dilatationalrheology showed that PPs form a stronger elastic shell at the pendantdrop interface, compared to HPs. The significantly high interfacialactivity obtained with PPs in this study highlights the importanceof the polymeric patchy shell and the spreading agent.
机译:在无表面活性剂的条件下,通过分别用聚苯乙烯和聚乙二醇(PEG)的二元配体混合物作为疏水性和亲水性配体进行官能化,制备了片状金纳米颗粒(PPs)。通过在水/空气和水/癸烷界面的悬垂液滴张力测定法,将PPs的界面活性与用PEG完全官能化的均质亲水性纳米颗粒(HPs)进行了比较。我们比较了三种不同的铺展剂的界面活性:水,水/氯仿和纯氯仿。我们发现,当铺展剂为水时,PPs的界面活性接近于零(约2 mN / m),而当铺展剂为水/氯仿时,其界面活性增加至约14 mN / m。当纳米颗粒用纯氯仿沉积时,通过压缩界面活性达到60 mN / m。在所有情况下,PP都比HP表现出更高的界面活性,而HP则没有界面活性,而与铺展剂无关。发现在水/癸烷界面的界面活性明显低于在水/空气界面的界面活性界面,因为PP在癸烷中聚集。界面膨胀流变学表明,PP在悬垂物上形成了更坚固的弹性壳与HP相比,drop接口。明显较高的界面在这项研究中通过PP获得的活性突出了重要性聚合物斑点状外壳和铺展剂。

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