Water, sulfur dioxide and nitric acid adsorption on calcium carbonate: A transmission and ATR-FTIR study

被引:222
作者
Al-Hosney, HA [1 ]
Grassian, VH [1 ]
机构
[1] Univ Iowa, Dept Chem, Iowa City, IA 52242 USA
关键词
D O I
10.1039/b417872f
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
Calcium carbonate (CaCO3) is a reactive component of mineral dust aerosol as well as buildings, statues and monuments. In this study, attenuated total reflection (ATR) and transmission Fourier transform infrared spectroscopy (FTIR) have been used to study the uptake of water, sulfur dioxide and nitric acid on CaCO3 particles at 296 K. Under atmospheric conditions, CaCO3 particles are terminated by a Ca(OH)(CO3H) surface layer. In the presence of water vapor between 5 and 95% relative humidity (RH), water molecularly adsorbs on the Ca(OH)(CO3H) surface resulting in the formation of an adsorbed thin water film. The adsorbed water film assists in the enhanced uptake of sulfur dioxide and nitric acid on CaCO3 in several ways. Under dry conditions (near 0% RH), sulfur dioxide and nitric acid react with the Ca(OH)(CO3H) surface to form adsorbed carbonic acid (H2CO3) along with sulfite and nitrate, respectively. Adsorbed carbonic acid is stable on the surface under vacuum conditions. Once the surface saturates with a carbonic acid capping layer, there is no additional uptake of gas-phase sulfur dioxide and nitric acid. However, upon adsorption of water, carbonic acid dissociates to form gaseous carbon dioxide and there is further uptake of sulfur dioxide and nitric acid. In addition, adsorbed water increases the mobility of the ions at the surface and enhances uptake of SO2 and HNO3. In the presence of adsorbed water, CaSO3 forms islands of a crystalline hydrate whereas Ca(NO3)(2) forms a deliquescent layer or micropuddles. Thus adsorbed water plays an important and multi-faceted role in the uptake of pollutant gases on CaCO3.
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页码:1266 / 1276
页数:11
相关论文
共 56 条
[1]   Phase transitions in calcium nitrate thin films [J].
Al-Abadleh, HA ;
Krueger, BJ ;
Ross, JL ;
Grassian, VH .
CHEMICAL COMMUNICATIONS, 2003, (22) :2796-2797
[2]   Phase transitions in magnesium nitrate thin films: A transmission FT-IR study of the deliquescence and efflorescence of nitric acid reacted magnesium oxide interfaces [J].
Al-Abadleh, HA ;
Grassian, VH .
JOURNAL OF PHYSICAL CHEMISTRY B, 2003, 107 (39) :10829-10839
[3]   Oxide surfaces as environmental interfaces [J].
Al-Abadleh, HA ;
Grassian, VH .
SURFACE SCIENCE REPORTS, 2003, 52 (3-4) :63-161
[4]   Carbonic acid: An important intermediate in the surface chemistry of calcium carbonate [J].
Al-Hosney, HA ;
Grassian, VH .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2004, 126 (26) :8068-8069
[5]  
ALABADLEH HA, 2004, IN PRESS J MOL CAT A
[6]   Role of NO2 and SO2 in degradation of limestone [J].
Allen, GC ;
El-Turki, A ;
Hallam, KR ;
McLaughlin, D ;
Stacey, M .
BRITISH CORROSION JOURNAL, 2000, 35 (01) :35-38
[7]   Water-induced reorganization of ultrathin nitrate films on NaCl: Implications for the tropospheric chemistry of sea salt particles [J].
Allen, HC ;
Laux, JM ;
Vogt, R ;
FinlaysonPitts, BJ ;
Hemminger, JC .
JOURNAL OF PHYSICAL CHEMISTRY, 1996, 100 (16) :6371-6375
[8]   THE EROSION OF CARBONATE STONE BY ACID-RAIN - LABORATORY AND FIELD INVESTIGATIONS [J].
BAEDECKER, PA ;
REDDY, MM .
JOURNAL OF CHEMICAL EDUCATION, 1993, 70 (02) :104-108
[9]  
BELOUSOV MV, 1970, SOV PHYS-SOLID STATE, V11, P2185
[10]   Modeling sulfur dioxide deposition on calcium carbonate [J].
Bernal, JLP ;
Bello, MA .
INDUSTRIAL & ENGINEERING CHEMISTRY RESEARCH, 2003, 42 (05) :1028-1034