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Understanding Trichloroethylene Chemisorption to Iron Surfaces Using Density Functional Theory

机译:使用密度泛函理论了解三氯乙烯对铁表面的化学吸附

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摘要

This research investigated the thermodynamic favorability and resulting structures for chemical adsorption of trichloroethylene (TCE) to metallic iron using periodic density functional theory (DFT). Three initial TCE positions having the plane defined by HCC atoms parallel to the iron surface resulted in formation of three different chemisorption complexes between carbon atoms in TCE and the iron surface. The Cl-bridge initial configuration with the HCC plane of the TCE molecule perpendicular to the iron surface did not result in C–Fe bond formation. The most energetically favorable complex formed at the C-bridge site where the initial configuration had the C=C bond in TCE at a bridge site between adjacent iron atoms. In the C-bridge complex one C atom formed two sigma bonds to different Fe atoms while the second C atom formed a sigma bond with a second Fe atom. Surface complexation at the C-bridge site resulted in scission of all three C–Cl bonds, and also resulted in a shortening of the C=C bond to a distance intermediate between a double and a triple bond. Initial configurations with the C=C bond adsorbed at top or hollow sites on the iron surface resulted in formation of C–Fe sigma bonds between a single C and two adjacent Fe atoms, and the scission of only two C–Cl bonds. Bond angles and bond lengths indicated that there were no changes in bond order of the C=C bond for top and hollow adsorption. Chemisorption at the C-bridge site had an early transition state in which all three C–Cl bonds were activated from ~1.7 to ~2.2 Å, with an activation energy of 49 kJ/mol. The early transition state and the loss of all three Cl atoms upon chemisorption are consistent with most experimental observations that TCE undergoes complete dechlorination in one interaction with the iron surface. The absence of chemisorption and scission of only two C–Cl bonds at the Cl-bridge site is consistent with experimental observations that trace amounts of chloroacetylene may also be produced from reactions of TCE with iron.
机译:这项研究使用周期性密度泛函理论(DFT)研究了三氯乙烯(TCE)对金属铁化学吸附的热力学有利性和所得结构。具有由HCC原子限定的平面平行于铁表面的三个初始TCE位置导致在TCE中的碳原子和铁表面之间形成三种不同的化学吸附络合物。 TCE分子的HCC平面垂直于铁表面的Cl桥初始构型不会导致C-Fe键形成。在初始构型在相邻铁原子之间的桥位处的TCE中具有C = C键的C桥位处形成了最有力的能量配合物。在C桥复合物中,一个C原子与不同的Fe原子形成两个sigma键,而第二个C原子与另一个Fe原子形成一个sigma键。 C桥位点的表面络合导致所有三个C–Cl键断裂,也导致C = C键缩短到双键和三键之间的中间距离。最初配置的C = C键吸附在铁表面的顶部或中空部位,导致单个C和两个相邻的Fe原子之间形成C-Feσ键,并且仅断裂两个C-Cl键。结合角和结合长度表明,对于顶部和空心吸附,C = C结合的结合顺序没有变化。 C桥位点的化学吸附具有一个早期过渡态,其中所有三个C–Cl键均从〜1.7到〜2.2Å被活化,活化能为49 kJ / mol。早期过渡态和化学吸附后所有三个Cl原子的损失与大多数实验观察结果一致,即TCE在与铁表面的一种相互作用中经历了完全脱氯。 Cl桥位上仅两个C–Cl键没有化学吸附和断裂,这与实验观察一致,即三氯乙烯(TCE)与铁的反应也可能产生痕量的氯乙炔。

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