Chemical Composition and Properties of the Liquid-Vapor Interface of Aqueous C1 to C4 Monofunctional Acid and Alcohol Solutions

被引:32
作者
Lee, Ming-Tao [1 ,2 ,5 ]
Orlando, Fabrizio [1 ]
Artiglia, Luca [1 ,3 ]
Chen, Shuzhen [1 ,4 ]
Ammann, Markus [1 ]
机构
[1] Paul Scherrer Inst, Environm Chem Lab, CH-5232 Villigen, Switzerland
[2] Univ Bern, Dept Chem & Biochem, CH-3012 Bern, Switzerland
[3] Paul Scherrer Inst, Lab Catalysis & Sustainable Chem, CH-5232 Villigen, Switzerland
[4] ETH, Inst Atmospher & Climate Sci, CH-8092 Zurich, Switzerland
[5] Stockholm Univ, Div Phys Chem, Dept Phys, SE-10691 Stockholm, Sweden
基金
瑞士国家科学基金会;
关键词
AIR-WATER-INTERFACE; RAY PHOTOELECTRON-SPECTROSCOPY; SURFACE-TENSION; ORGANIC-COMPOUNDS; GAS-PHASE; PHOTOSENSITIZED PRODUCTION; AIR/WATER INTERFACE; THERMODYNAMIC MODEL; CARBOXYLATE IONS; PHOTOEMISSION;
D O I
10.1021/acs.jpca.6b09261
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The liquid-vapor interface is playing an important role in aerosol and cloud chemistry in cloud droplet activation by aerosol particles and potentially also in ice nucleation. We have employed the surface sensitive and chemically selective X-ray photoelectron spectroscopy (XPS) technique to examine the liquid vapor interface for mixtures of water and small alcohols or small carboxylic acids (C1 to C4), abundant chemicals in the atmosphere in concentration ranges relevant for cloud chemistry or aerosol particles at the point of activation into a cloud droplet. A linear correlation was found between the headgroup carbon is core-level signal intensity and the surface excess derived from literature surface tension data with the offset being explained by the bulk contribution to the photoemission signal. The relative interfacial enhancement of the carboxylic acids over the carboxylates at the same bulk concentration was found to be highest (nearly 20) for propionic acid/propionate and still about S for formic acid/formate, also in fair agreement with surface tension measurements. This provides direct spectroscopic evidence for high carboxylic acid concentrations at aqueous solution air interfaces that may be responsible for acid catalyzed chemistry under moderately acidic conditions with respect to their bulk aqueous phase acidity constant. By assessing the ratio of aliphatic to headgroup C is signal intensities XPS also provides information about the orientation of the molecules. The results indicate an increasing orientation of alcohols and neutral acids toward the surface normal as a function of chain length, along with increasing importance of lateral hydrophobic interactions at higher surface coverage. In turn, the carboxylate ions exhibit stronger orientation toward the surface normal than the corresponding neutral acids, likely caused by the stronger hydration of the charged headgroup.
引用
收藏
页码:9749 / 9758
页数:10
相关论文
共 75 条
  • [1] ABRAMZON AA, 1993, RUSS J APPL CHEM+, V66, P1473
  • [2] Dihedral angle of lens and interfacial tension of air long chain alcohol water systems
    Aratono, M
    Toyomasu, T
    Shinoda, T
    Ikeda, N
    Takiue, T
    [J]. LANGMUIR, 1997, 13 (07) : 2158 - 2163
  • [3] Surface tension and density of binary mixtures of monoalcohols, water and acetonitrile: equation of correlation of the surface tension
    Belda Maximino, R.
    [J]. PHYSICS AND CHEMISTRY OF LIQUIDS, 2009, 47 (05) : 475 - 486
  • [4] Parameter Interpretation and Reduction for a Unified Statistical Mechanical Surface Tension Model
    Boyer, Hallie
    Wexler, Anthony
    Dutcher, Cari S.
    [J]. JOURNAL OF PHYSICAL CHEMISTRY LETTERS, 2015, 6 (17): : 3384 - 3389
  • [5] Statistical Thermodynamic Model for Surface Tension of Aqueous Organic Acids with Consideration of Partial Dissociation
    Boyer, Hallie C.
    Dutcher, Cari S.
    [J]. JOURNAL OF PHYSICAL CHEMISTRY A, 2016, 120 (25) : 4368 - 4375
  • [6] Determination of Surface Potential and Electrical Double-Layer Structure at the Aqueous Electrolyte-Nanoparticle Interface
    Brown, Matthew A.
    Abbas, Zareen
    Kleibert, Armin
    Green, Richard G.
    Goel, Alok
    May, Sylvio
    Squires, Todd M.
    [J]. PHYSICAL REVIEW X, 2016, 6 (01):
  • [7] Ion Spatial Distributions at the Air- and Vacuum-Aqueous K2CO3 Interfaces
    Brown, Matthew A.
    Lee, Ming-Tao
    Kleibert, Armin
    Ammann, Markus
    Giorgi, Javier B.
    [J]. JOURNAL OF PHYSICAL CHEMISTRY C, 2015, 119 (09) : 4976 - 4982
  • [8] A new endstation at the Swiss Light Source for ultraviolet photoelectron spectroscopy, X-ray photoelectron spectroscopy, and X-ray absorption spectroscopy measurements of liquid solutions
    Brown, Matthew A.
    Redondo, Amaia Beloqui
    Jordan, Inga
    Duyckaerts, Nicolas
    Lee, Ming-Tao
    Ammann, Markus
    Nolting, Frithjof
    Kleibert, Armin
    Huthwelker, Thomas
    Maechler, Jean-Pierre
    Birrer, Mario
    Honegger, Juri
    Wetter, Reto
    Woerner, Hans Jakob
    van Bokhoven, Jeroen A.
    [J]. REVIEW OF SCIENTIFIC INSTRUMENTS, 2013, 84 (07)
  • [9] Electronic Structures of Formic Acid (HCOOH) and Formate (HCOO-) in Aqueous Solutions
    Brown, Matthew A.
    Vila, Fernando
    Sterrer, Martin
    Thuermer, Stephan
    Winter, Bernd
    Ammann, Markus
    Rehr, John J.
    van Bokhoven, Jeroen A.
    [J]. JOURNAL OF PHYSICAL CHEMISTRY LETTERS, 2012, 3 (13): : 1754 - 1759
  • [10] Brown MA, 2009, ANNU REP PROG CHEM C, V105, P174, DOI 10.1039/b803023p