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强结合的十二烷基硫酸钠围绕单壁碳纳米管。

Strongly Bound Sodium Dodecyl Sulfate Surrounding Single-Wall Carbon Nanotubes.

机构信息

Department of Chemistry, Elon University , Elon, North Carolina 27244, United States.

出版信息

Langmuir. 2017 May 23;33(20):5006-5014. doi: 10.1021/acs.langmuir.7b00758. Epub 2017 May 9.

Abstract

NMR techniques have been widely used to infer molecular structure, including surfactant aggregation. A combination of optical spectroscopy, proton NMR spectroscopy, and pulsed field gradient NMR (PFG NMR) is used to study the adsorption number for sodium dodecyl sulfate (SDS) with single-wall carbon nanotubes (SWCNTs). Distinct transitions in the NMR chemical shift of SDS are observed in the presence of SWCNTs. These transitions demonstrate that micelle formation is delayed by SWCNTs due to the adsorption of SDS on the nanotube surface. Once the nanotube surface is saturated, the free SDS concentration increases until micelle formation is observed. Therefore, the adsorption number of SDS on SWCNTs can be determined by the changes to the apparent critical micelle concentration (CMC). PFG NMR found that SDS remains strongly bound onto the nanotube. Quantitative analysis of the diffusivity of SDS allowed calculation of the adsorption number of strongly bound SDS on SWCNTs. The adsorption numbers from these techniques give the same values within experimental error, indicating that a significant fraction of the SDS interacting with nanotubes remains strongly bound for as long as 0.5 s, which is the maximum diffusion time used in the PFG NMR measurements.

摘要

NMR 技术已被广泛应用于推断分子结构,包括表面活性剂聚集。本文采用光学光谱、质子 NMR 光谱和脉冲梯度 NMR(PFG NMR)相结合的方法,研究了十二烷基硫酸钠(SDS)在单壁碳纳米管(SWCNTs)上的吸附数。在 SWCNTs 的存在下,SDS 的 NMR 化学位移发生了明显的转变。这些转变表明,由于 SDS 在纳米管表面的吸附,SWCNTs 延迟了胶束的形成。一旦纳米管表面饱和,游离 SDS 浓度增加,直到观察到胶束形成。因此,通过观察表观临界胶束浓度(CMC)的变化,可以确定 SDS 在 SWCNTs 上的吸附数。PFG NMR 发现 SDS 仍然强烈结合在纳米管上。通过对 SDS 扩散性的定量分析,可以计算出 SWCNTs 上强结合 SDS 的吸附数。这些技术的吸附数在实验误差范围内给出了相同的值,表明与纳米管相互作用的 SDS 有很大一部分在 0.5 s 的最大扩散时间内仍然强烈结合。

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