期刊
JOURNAL OF PHYSICAL CHEMISTRY C
卷 127, 期 17, 页码 8399-8410出版社
AMER CHEMICAL SOC
DOI: 10.1021/acs.jpcc.3c02312
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In this study, the adsorption of carbaryl to hydrophilic silica surfaces was investigated using vibrational Sum Frequency Generation (vSFG) spectroscopy and atomistic simulations. The results show that carbaryl molecules readily adsorb to silica/air interfaces through hydrogen-bonding interactions with the surface silanols and silenolates. The orientation of the naphthyl aromatic ring is roughly parallel to the surface. This characterization of carbamate pesticides at silica surfaces is important for understanding their transport, stabilization, and potential degradation mechanisms in the environment.
Carbaryl (1-naphthyl-N-methyl carbamate) is one of the most abundantly used carbamate pesticides and a common ground and surface water contaminant. Despite this, there is a lack of understanding regarding the specific interactions between this pesticide and mineral particles with environmental impact, including soil and dust aerosol interfaces. Here, we examine the adsorption of carbaryl to hydrophilic silica surfaces by applying a combination of vibrational Sum Frequency Generation (vSFG) spectroscopy and atomistic simulations. We find that carbaryl molecules readily adsorb to silica/air interfaces by hydrogen-bonding interactions between the carbamate group (primarily the -NH terminus, secondarily the ester -C=O ester moiety) and the surface silanols and silenolates. On average, this results in the naphthyl aromatic ring being oriented roughly parallel to the surface. Our characterization of interactions of carbamate pesticides at silica surfaces is particularly valuable for understanding the transport, stabilization, and potential degradation mechanisms of carbamate pesticides by interfaces during downstream processes of environmental relevance.
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