Kido Soule Melissa C, Blower Patrick G, Richmond Geraldine L
Department of Chemistry, University of Oregon, 1253 University of Oregon, Eugene, Oregon 97403, USA.
J Phys Chem A. 2007 May 3;111(17):3349-57. doi: 10.1021/jp0686994. Epub 2007 Apr 10.
Nitric acid plays an important role in the heterogeneous chemistry of the atmosphere. Reactions involving HNO(3) at aqueous interfaces in the stratosphere and troposphere depend on the state of nitric acid at these surfaces. The vapor/liquid interface of HNO(3)-H2O binary solutions and HNO(3)-H(2)SO(4)-H2O ternary solutions are examined here using vibrational sum frequency spectroscopy (VSFS). Spectra of the NO2 group at different HNO(3) mole fractions and under different polarization combinations are used to develop a detailed picture of these atmospherically important systems. Consistent with surface tension and spectroscopic measurements from other laboratories, molecular nitric acid is identified at the surface of concentrated solutions. However, the data here reveal the adsorption of two different hydrogen-bonded species of undissociated HNO(3) in the interfacial region that differ in their degree of solvation of the nitro group. The adsorption of these undissociated nitric acid species is shown to be sensitive to the H2O:HNO(3) ratio as well as to the concentration of sulfuric acid.
硝酸在大气的多相化学中起着重要作用。平流层和对流层中涉及硝酸(HNO₃)在水界面的反应取决于这些表面上硝酸的状态。本文使用振动和频光谱(VSFS)研究了HNO₃-H₂O二元溶液和HNO₃-H₂SO₄-H₂O三元溶液的气/液界面。利用不同硝酸摩尔分数和不同偏振组合下NO₂基团的光谱来详细描绘这些对大气重要的体系。与其他实验室的表面张力和光谱测量结果一致,在浓溶液表面鉴定出了分子态硝酸。然而,这里的数据揭示了在界面区域存在两种不同的未离解HNO₃氢键物种,它们的硝基溶剂化程度不同。结果表明,这些未离解硝酸物种的吸附对H₂O:HNO₃比例以及硫酸浓度敏感。