Dissolved organic matter removal and disinfection byproduct formation control using ion exchange

被引:58
作者
Tan, YR
Kilduff, JE
Kitis, M
Karanfil, T
机构
[1] Rensselaer Polytech Inst, Dept Civil & Environm Engn, Troy, NY 12180 USA
[2] Suleyman Demirel Univ, Dept Environm Engn, TR-32200 Isparta, Turkey
[3] Clemson Univ, Dept Environm Engn & Sci, Anderson, SC 29625 USA
基金
美国国家科学基金会;
关键词
NOM; DOM; DBP formation; ion exchange; THM; HAA; SUVA;
D O I
10.1016/j.desal.2004.10.019
中图分类号
TQ [化学工业];
学科分类号
0817 ;
摘要
Three different ion exchange resins were evaluated for their ability to remove dissolved organic matter (DOM) and reduce formation of disinfection byproducts (DBPs) formed during chlorination of surface waters sampled from the Intercoastal Waterway, Myrtle Beach, SC, USA (MB water), and the Tomhannock Reservoir, Troy, NY, USA (TMK water). At resin doses up to 600 mg/L, DOC levels were reduced from 30 to 70%, while total trihalomethane and haloacetic acid formation reactivity (i.e., TTHM/DOC and HAA9/DOC) was reduced from 40 to 70% and 50%, respectively. This suggests that ion exchange, alone or in combination with other processes, holds promise for removing a broad spectrum of DBP precursors. Chloride release was measured to confirm an ion exchange mechanism, but the possibility of physisorption and hydrogen bonding mechanisms was not ruled out. Ion exchange appeared to selectively remove high-specific UV-absorbing (i.e., SUVA(254)) DOM components from the TMK water; these components also had the highest molecular weights. However, this was not the case for the MB water. The "SUVA(254) profile", the relationship between SUVA(254) and DBP formation reactivity (TTHM/DOC and HAA9/DOC), showed significant differences from the patterns observed previously for separation processes (e.g., coagulation and activated carbon adsorption) that rely primarily on hydrophobic interactions as a separation mechanism.
引用
收藏
页码:189 / 200
页数:12
相关论文
共 36 条
[1]   ISOLATION OF HYDROPHILIC ORGANIC-ACIDS FROM WATER USING NONIONIC MACROPOROUS RESINS [J].
AIKEN, GR ;
MCKNIGHT, DM ;
THORN, KA ;
THURMAN, EM .
ORGANIC GEOCHEMISTRY, 1992, 18 (04) :567-573
[2]  
AMY GL, 1992, J AM WATER WORKS ASS, V84, P67
[3]   Removal of THM precursors by coagulation or ion exchange [J].
Bolto, B ;
Dixon, D ;
Eldridge, R ;
King, S .
WATER RESEARCH, 2002, 36 (20) :5066-5073
[4]   Removal of natural organic matter by ion exchange [J].
Bolto, B ;
Dixon, D ;
Eldridge, R ;
King, S ;
Linge, K .
WATER RESEARCH, 2002, 36 (20) :5057-5065
[5]   MOLECULAR-WEIGHT EFFECTS ON THM CONTROL BY COAGULATION AND ADSORPTION [J].
CHADIK, PA ;
AMY, GL .
JOURNAL OF ENVIRONMENTAL ENGINEERING-ASCE, 1987, 113 (06) :1234-1248
[6]   MOLECULAR-WEIGHT, POLYDISPERSITY, AND SPECTROSCOPIC PROPERTIES OF AQUATIC HUMIC SUBSTANCES [J].
CHIN, YP ;
AIKEN, G ;
OLOUGHLIN, E .
ENVIRONMENTAL SCIENCE & TECHNOLOGY, 1994, 28 (11) :1853-1858
[7]  
Chow CWK, 1999, WATER SCI TECHNOL, V40, P97, DOI 10.1016/S0273-1223(99)00645-9
[8]  
CROUE JP, 1999, 217 ACS NAT M AN CA, P218
[9]  
DICKENSON ERV, 1999, 217 ACS NAT M AN CA, P122
[10]  
EDZWALD JK, 1985, J AM WATER WORKS ASS, V77, P122