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首页> 外文期刊>The Journal of Chemical Physics >Partially (resp. fully) reversible adsorption of monoterpenes (resp. alkanes and cycloalkanes) to fused silica
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Partially (resp. fully) reversible adsorption of monoterpenes (resp. alkanes and cycloalkanes) to fused silica

机译:部分(resp。完全)可逆吸附单波选(烷烃和环烷烃)融合二氧化硅

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摘要

This work compares the extent of reversibility and the thermodynamics of adsorption (K-ads, Delta G degrees(ads)) of room-temperature vapors of common environmentally relevant monoterpenes (alpha-pinene, beta-pinene, limonene, and 3-carene) and industrially relevant cyclic and acyclic non-terpene hydrocarbons (cyclohexane, hexane, octane, and cyclooctane) to fused silica surfaces. Vibrational sum frequency generation spectroscopy carried out in the C-H stretching region shows negligible surface coverage-dependent changes in the molecular orientation of all species surveyed except for cyclohexane. The group of monoterpenes studied here distinctly exhibits partially reversible adsorption to fused silica surfaces compared to the group of non-terpene hydrocarbons, demonstrating a link between molecular structure and adsorption thermodynamics. The standard Gibbs free energy of adsorption is nonlinearly correlated with the equilibrium vapor pressure of the compounds surveyed. Published under license by AIP Publishing.
机译:这项工作比较了普通环保型单体萜的室温蒸汽的吸附(K-ADS,Delta G度(ADS)的可逆性和热力学的程度(α-叉烯,β-甲烯,柠檬烯和3-甲烯)和工业相关的环状和无环非萜烯烃(环己烷,己烷,辛烷值和环辛烷)与熔融二氧化硅表面。在C-H拉伸区域中进行的振动和频生成光谱显示除了环己烷之外,所接受调查的所有物种的分子取向的可忽略的表面覆盖依赖性变化。与非萜烯烃组相比,这里研究的单波通小组明显地表现出对熔融二氧化硅表面的部分可逆吸附,证明了分子结构和吸附热力学之间的联系。标准Gibbs吸附能量与调查的化合物的平衡蒸气压无线相关。通过AIP发布在许可证下发布。

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