Photochemical transformation of acrylic acid in seawater

被引:13
作者
Wu, Xi [1 ]
Liu, Chun-Ying [1 ]
Li, Pei-Feng [1 ]
机构
[1] Ocean Univ China, Coll Chem & Chem Engn, Key Lab Marine Chem Theory & Technol, Minist Educ, Qingdao 266100, Peoples R China
基金
中国国家自然科学基金;
关键词
Seawater; Acrylic acid (AA); Photochemical degradation; Microbial degradation rates; Kinetic studies; Jiaozhou Bay; DIMETHYL SULFIDE; PHOTO-OXIDATION; OCEANIC PHYTOPLANKTON; HUMIC SUBSTANCES; SURFACE WATERS; NATURAL-WATERS; SULFUR CYCLE; ATMOSPHERE; SEA; CLIMATE;
D O I
10.1016/j.marchem.2015.01.003
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Acrylic acid (AA), a short-chain fatty acid found in the ocean, is derived from the microbial cleavage of dimethylsulfoniopropionate in addition to terrestrial input. The aqueous photochemical transformation of AA in natural seawater, artificial seawater, and Milli-Q water was studied under artificial light (using a photochemical reactor) and natural light (by exposure to sunlight). A degradation study on field seawater was conducted inside and outside Jiaozhou Bay, which is located in the north of China. Kinetic studies showed that the degradation and reaction rate of AA in natural seawater were obviously higher than those in the other aqueous media under artificial and natural light, with the degradation characteristics in artificial seawater and Milli-Q water being similar. The degradation and reaction rate of AA in natural seawater significantly increased with decreased concentration. AA in different media exhibited relatively lower reaction rates under natural light than those under artificial light. However, AA at different concentrations had similar degradation and reaction rates under these two irradiation types. Visible light seemed more efficient for the degradation reaction than ultraviolet A and ultraviolet B rays. The concentrations and degradation of AA inside and outside the Jiaozhou Bay showed significantly seasonal variations, and the photochemical and microbial degradation both showed the maximum rates in autumn. The photochemical reaction rates were found to be lower than the microbial degradation rates in four seasons. The photochemical degradation inside the bay was always lower than that outside. The photochemical transformation of AA depended on seawater composition and field conditions. (C) 2015 Elsevier B.V. All rights reserved.
引用
收藏
页码:29 / 36
页数:8
相关论文
共 52 条
[1]   OCEAN-ATMOSPHERE INTERACTIONS IN THE GLOBAL BIOGEOCHEMICAL SULFUR CYCLE [J].
ANDREAE, MO .
MARINE CHEMISTRY, 1990, 30 (1-3) :1-29
[2]   THE MARINE CHEMISTRY OF DIMETHYLSULFIDE [J].
ANDREAE, MO ;
BARNARD, WR .
MARINE CHEMISTRY, 1984, 14 (03) :267-279
[3]   DIMETHYL SULFIDE IN THE MARINE ATMOSPHERE [J].
ANDREAE, MO ;
FEREK, RJ ;
BERMOND, F ;
BYRD, KP ;
ENGSTROM, RT ;
HARDIN, S ;
HOUMERE, PD ;
LEMARREC, F ;
RAEMDONCK, H ;
CHATFIELD, RB .
JOURNAL OF GEOPHYSICAL RESEARCH-ATMOSPHERES, 1985, 90 (D7) :2891-2900
[4]  
Andreae MO, 1986, ROLE AIR SEA EXCHANG, V185, P331
[5]  
[Anonymous], ANN REV PLANT PHYSL
[6]   The aqueous photochemical transformation of acrylic acid [J].
Bajt, O ;
Sket, B ;
Faganeli, J .
MARINE CHEMISTRY, 1997, 58 (3-4) :255-259
[7]   REGIONAL AND SEASONAL-VARIATIONS IN THE FLUX OF OCEANIC DIMETHYLSULFIDE TO THE ATMOSPHERE [J].
BATES, TS ;
CLINE, JD ;
GAMMON, RH ;
KELLYHANSEN, SR .
JOURNAL OF GEOPHYSICAL RESEARCH-OCEANS, 1987, 92 (C3) :2930-2938
[8]   THE ROLE OF THE OCEAN IN A REGIONAL SULFUR CYCLE [J].
BATES, TS ;
CLINE, JD .
JOURNAL OF GEOPHYSICAL RESEARCH-OCEANS, 1985, 90 (NC5) :9168-9172
[9]   THE INFLUENCE OF LIGHT AND TEMPERATURE ON CARBON-SPECIFIC DMS RELEASE BY CULTURES OF PHAEOCYSTIS-ANTARCTICA AND 3 ANTARCTIC DIATOMS [J].
BAUMANN, MEM ;
BRANDINI, FP ;
STAUBES, R .
MARINE CHEMISTRY, 1994, 45 (1-2) :129-136
[10]  
Berresheim H., 1990, J ATMOS CHEM, V15, P39