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Aqueous-phase behavior of glyoxal and methylglyoxal observed with carbon and oxygen K-edge X-ray absorption spectroscopy

机译:用碳和氧k边射线吸收光谱观察乙二醛和甲基乙二醛的水相行为

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Glyoxal ( CHOCHO ) and methylglyoxal ( CH 3 C(O)CHO ) are well-known components of atmospheric particles and their properties can impact atmospheric chemistry and cloud formation. To get information on their hydration states in aqueous solutions and how they are affected by the addition of inorganic salts (sodium chloride ( NaCl ) and sodium sulfate ( Na 2 SO 4 )), we applied carbon and oxygen K-edge X-ray absorption spectroscopy (XAS) in transmission mode. The recorded C K-edge spectra show that glyoxal is completely hydrated in the dilute aqueous solutions, in line with previous studies. For methylglyoxal, supported by quantum chemical calculations we identified not only C–H, C=O and C–OH bonds, but also fingerprints of C–OH(CH 2 ) and C=C bonds. The relatively low intensity of C=O transitions implies that the monohydrated form of methylglyoxal is not favored in the solutions. Instead, the spectral intensity is stronger in regions where products of aldol condensation and enol tautomers of the monohydrates contribute. The addition of salts was found to introduce only very minor changes to absorption energies and relative intensities of the observed absorption features, indicating that XAS in the near-edge region is not very sensitive to these intermolecular organic–inorganic interactions at the studied concentrations. The identified structures of glyoxal and methylglyoxal in an aqueous environment support the uptake of these compounds to the aerosol phase in the presence of water and their contribution to secondary organic aerosol formation.
机译:乙二醛(CHOCHO)和甲基乙二醛(CH 3 C(O)CHO)是大气颗粒的公知成分,其性质可以影响大气化学和云形成。为了在水溶液中获取有关水合态的信息以及它们如何通过加入无机盐(氯化钠)和硫酸钠(Na 2 SO 4)的影响,我们施加碳和氧k缘X射线吸收传输模式中的光谱学(XAS)。记录的C k-Edge光谱显示,乙醛在稀水溶液中完全水合,与先前的研究一致。对于甲基乙二醛,由量子化学计算支持,我们不仅鉴定了C-H,C = O和C-OH键,还识别C-OH(CH 2)和C = C键的指纹。 C = O转变的相对低强度意味着甲基乙二醛的一水化形式在溶液中不受偏爱。相反,磷脂缩合和单水合物的烯醇缩放剂的产物中的谱强度较强。发现添加盐仅引入吸收能量和观察到的吸收特征的相对强度的较小变化,表明近边缘区域中的XA对所研究浓度的这些分子间有机 - 无机相互作用不太敏感。含水环境中乙二醛和甲基乙二醛的鉴定结构支持水中的气溶胶相的吸收,并在水的存在下对次级有机气溶胶形成的贡献。

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