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In situ FT-IR measurements of competitive vapor adsorption into porous thin films containing silica nanoparticles

机译:现场FT-IR测量竞争性蒸气吸附到包含二氧化硅纳米颗粒的多孔薄膜中

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摘要

Vapor adsorption into porous ultrathin films on a gold surface is investigated with in situ surface plasmon resonance (SPR) and polarization-modulation infrared reflection-absorption spectroscopy (PM-IRRAS). The thin films are prepared by the electrostatic self-assembly of oppositely charged poly(L-lysine) (PL) and silica nanoparticles on a chemically modified gold surface. Characterization,with ex situ SPR and PM-IRRAS demonstrates the buildup of multiple PL/SiO2 bilayers as well as an excellent correlation between the quantitative results from these two techniques. In situ vapor adsorption experiments with these thin films show evidence of porosity, reproducibility, and rapid reversibility. Exposure to acetone vapor (P/P-0 = 0.032) causes the film to adsorb 9% acetone by volume, which corresponds to coverage of approximately one-half of the silica nanoparticle surface area. In situ PM-IRRAS provides much information about the molecular interactions occurring in the film upon adsorption or desorption of vapors. Dosing with a mixture of vapors leads to a competition for adsorption into the film, and PM-IRRAS results show that acetone slightly out-competes nitromethane. These experiments with nanoparticle thin films demonstrate the advantages of using in situ PM-IRRAS for studying reversible adsorption in the presence of vapor mixtures. [References: 43]
机译:利用原位表面等离子体激元共振(SPR)和偏振调制红外反射吸收光谱法(PM-IRRAS)研究了金表面多孔超薄膜上的蒸气吸附。通过在化学修饰的金表面上带相反电荷的聚(L-赖氨酸)(PL)和二氧化硅纳米粒子进行静电自组装来制备薄膜。通过异位SPR和PM-IRRAS进行的表征证明了多层PL / SiO2双层的形成以及这两种技术的定量结果之间的良好相关性。用这些薄膜进行的原位蒸气吸附实验显示出孔隙率,可再现性和快速可逆性。暴露于丙酮蒸汽中(P / P-0 = 0.032)使薄膜吸附9%的丙酮(体积),这相当于覆盖了二氧化硅纳米粒子表面积的大约一半。原位PM-IRRAS提供了许多有关蒸气吸附或解吸时薄膜中发生的分子相互作用的信息。混合使用蒸汽会导致吸附进入薄膜的竞争,而PM-IRRAS结果表明,丙酮略胜于硝基甲烷。这些使用纳米颗粒薄膜的实验证明了使用原位PM-IRRAS来研究在存在蒸汽混合物的情况下可逆吸附的优势。 [参考:43]

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