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吸附水对柠檬烯与羟基化二氧化硅相互作用的影响:在潮湿环境中π氢键对表面的影响。

Impact of Adsorbed Water on the Interaction of Limonene with Hydroxylated SiO: Implications of π-Hydrogen Bonding for Surfaces in Humid Environments.

机构信息

Department of Chemistry, University of California, Irvine, California 92697, United States.

Department of Chemistry and Biochemistry, University of California-San Diego, La Jolla, California 92093, United States.

出版信息

J Phys Chem A. 2020 Dec 17;124(50):10592-10599. doi: 10.1021/acs.jpca.0c08600. Epub 2020 Dec 4.

Abstract

The indoor environment is a dynamic one with many variables impacting indoor air quality and indoor air chemistry. These include relative humidity (RH) and the presence of different surfaces. Although it has been suggested that the indoor concentrations of gas-phase compounds increase at higher relative humidity, because of displacement of these compounds from indoor surfaces, little is known from a molecular perspective about how RH and adsorbed water impact the adsorption of indoor relevant organic compounds such as limonene with indoor relevant surfaces. Herein, we investigate the effects of RH on the adsorption of limonene, a hydrophobic molecule, on hydroxylated SiO surfaces, a model for glass surfaces. Experimental data using infrared spectroscopy to directly measure limonene adsorption are combined with both force field-based molecular dynamics (MD) and ab initio molecular dynamics (AIMD) simulations to understand the competitive interactions between limonene, water, and the SiO surface. The spectroscopic data provide evidence that adsorbed limonene is not completely displaced by adsorbed water, even at high RH (∼80%) when the water layer coverage is close to three monolayers (MLs). These experimental data are supported by AIMD and MD simulations, which indicate that limonene is present at the adsorbed water interface but displaced from direct interactions with SiO. This study shows that although some limonene can desorb from the surface, even at the highest RH, more than half the limonene remains adsorbed on the surface that can undergo continued surface reactivity. A complex network of π-hydrogen bonds, water-water hydrogen bonds, and SiO-water hydrogen bonds explains these interactions at the air/adsorbed water/SiO interface that hold the hydrophobic limonene molecule at the interface. Importantly, these interactions are most likely present for a range of other systems involving organic compounds and solid surfaces at ambient relative humidity and may be important in a range of scientific areas, from sensor development to cultural heritage science.

摘要

室内环境是一个动态的环境,有许多变量会影响室内空气质量和室内空气化学。这些变量包括相对湿度 (RH) 和不同表面的存在。尽管有人认为,由于这些化合物从室内表面被置换,气相化合物的室内浓度会随着相对湿度的升高而增加,但从分子角度来看,相对湿度和吸附水如何影响例如柠檬烯等与室内相关的有机化合物在与室内相关的表面上的吸附,人们知之甚少。在此,我们研究了相对湿度对疏水分子柠檬烯在羟化 SiO 表面上吸附的影响,SiO 表面是玻璃表面的模型。使用红外光谱直接测量柠檬烯吸附的实验数据与基于力场的分子动力学 (MD) 和从头算分子动力学 (AIMD) 模拟相结合,以了解柠檬烯、水和 SiO 表面之间的竞争相互作用。光谱数据表明,即使在相对湿度较高(约 80%)时,水层覆盖率接近三个单层(MLs),吸附的水也不会完全置换吸附的柠檬烯。这些实验数据得到了 AIMD 和 MD 模拟的支持,这些模拟表明,柠檬烯存在于吸附水界面,但与 SiO 没有直接相互作用。这项研究表明,尽管一些柠檬烯可以从表面解吸,即使在最高 RH 下,仍有超过一半的柠檬烯留在表面上,可以继续发生表面反应。在空气/吸附水/SiO 界面处,π氢键、水-氢键和 SiO-氢键的复杂网络解释了这些相互作用,将疏水分子柠檬烯固定在界面处。重要的是,这些相互作用很可能存在于涉及有机化合物和固-液界面的其他系统中,在环境相对湿度下,它们可能在从传感器开发到文化遗产科学的一系列科学领域中具有重要意义。

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