Browse > Article

Characteristics of Chlorination Byproducts Formation of Amino Acid Compounds  

Son, Hee-Jong (Water Quality Institute, Busan Water Authority)
Choi, Young-Ik (Department of Environmental Engineering, Silla University)
Bae, Sang-Dae (Department of Environmental Engineering, Silla University)
Jung, Chul-Woo (Ulsan Regional Innovation Agency, Ulsan Industry Promotion Techno Park)
Publication Information
Abstract
This study was conducted to analyze and determine formation potentials for chlorination disinfection by-products (DBPs) from twenty amino acid compounds with or without $Br^-$. Two of twenty amino acid compound were tryptophan and tyrosine that were relatively shown high for formation of trihalomethanes (THMs)/dissolved organic carbon (DOC) whether or not $Br^-$ presented. Other 18 compounds were shown low for formation of THMs/DOC whether or not $Br^-$ presented. Five amino acid compounds that were tryptophan, tyrosine, asparagine, aspartic acid and histidine were shown high for formation of haloacetic acids (HAAs)/DOC whether or not $Br^-$ presented. Although formation of dichloroacetic acid (DCAA) was dominated in asparagine, aspartic acid and histidine, trichloroacetic acid (TCAA) was dominated in tryptophan and tryptophan. The formation of haloacetnitriles (HANs)/DOC whether or not $Br^-$ presented was high in Aspartic acid, histidine, asparagine, tyrosine and tryptophan. Specially, aspartic acid was detected 660.2 ${\mu}$g/mg (HAN/DOC). Although the formation of chloralhydrate (CH)/DOC was shown high in asparagine, aspartic acid, histidine, methionine, tryptophan and tyrosine, the formation of Chloropicrin (CP)/DOC was low (1 ${\mu}$g/mg) in twenty amino acid compounds. The formations of THM, HAA and HAN were also investigated in functional groups of amino acids. The highest formation of THM was shown in amino acids compounds (tryptophan and tyrosine) with an aromatic functional group. Highest, second-highest, third-highest and fourth-highest functional groups for formation of HAA were aromatic, neutral, acidic and basic respectively. In order of increasing functional groups for formation of HAN were acidic, basic, neutral and aromatic.
Keywords
Chlorination By-Products; Amino Acid Compounds; Trihalomethane; Haloacetic Acid; Haloacetonitrile; Chloral Hydrate;
Citations & Related Records
Times Cited By KSCI : 2  (Citation Analysis)
연도 인용수 순위
1 Craun, G. F., Bull, R. J., Clark, R. M., Doull, J., Grabow, W., Marsh, G. M., Okun, D. A, Regli, S., Sobsey, M. D., and Symons, J. M., "Balancing chemical and microbial risks of drinking water disinfection. part I. benefits and potential risks," Water Supply: Research & Technology-Aqua, 43, 192-199(1994)
2 Cowman, G. A. and Singer, P. C., "Effect of bromide ion on haloacetic acid speciation resulting from chlorination and chloramination of aquatic humic substances," Environ. Sci. Technol., 30(1), 16-24(1996)   DOI   ScienceOn
3 Yang, X. and Shang, C., "Chlorination byproduct formation in the presence of humic acid, model nitrogenous organic compounds, ammonia and bromide," Environ. Sci. Technol., 38(19), 4995-5001(2004)   DOI   ScienceOn
4 Keith, L. H., Hall, R. C., Hanisch, R. C., Landolt, R. G., and Henderson, J. E., "New methods for analyzing water pollutants," Water Sci. Technol., 14, 59-71(1982)
5 Bull, R. J. and Robinson, M., "Carcinogenic activity of haloacetonitrile and haloacetone derivatives in the mouse skin and lung," In Water Chlorination, Chemistry, Environmental Impact and Health effects, 5, pp. 221-227(1983)
6 Oliver, B. G., "Dihaloacetonitriles in drinking water: algae and fulvic acid as precursors," Environ. Sci. Technol., 17(2), 80(1983)   DOI   ScienceOn
7 U.S. EPA National Exposure Research Laboratory, Office of Research and Development, Method 552.3., Cincinnati, Ohio.(2003)
8 Nweke, A. and Scully, F. E., "Stable N-chloroaldimines and other products of the chlorination of iosleucine in model solutions and in a waste-water," Environ. Sci. Technol., 23, 989-994(1989)   DOI   ScienceOn
9 Hureiki, L., Croue, J. P., and Legube, B., "Chlorination studies of free and combined amino-acids," Water Res., 28, 2521-2523(1994)   DOI   ScienceOn
10 Goslan, E. H., Jefferson, B., Jarvis, P. R, and Parson, S. A., "Aquatic natural organic matter (NOM): will it form THMs or HAAs?," Proceedings of IWA World Water Congress, September 10-14, Beijing, China(2008)
11 Babcock, D. V. and Singer, P. C., "Chlorination and coagulation of humic and fulvic acids," J. AWWA, 71(3), 149(1979)
12 Krasner, B. S. W., McGuire, M. J., Jacangelo, J. G., Patania, N. L., Reagan, K. M., and Aieta, E. M., "The occurrence of disinfection by-products in U.S. drinking water," J. AWWA, 81(8), 41(1989)
13 Chang, E. E., Lin, Y. P., and Chiang, P. C., "Effects of bromide on the formation of THMs and HAAs," Chemosphere, 43, 1029-1034(2001)   DOI   ScienceOn
14 Chin, Y. P., Aiken, G. O., and Loughlin, E. O., "Molecular weight, polydispersity and spectroscopic properties of aquatic humic substances," Environ. Sci. Technol., 28(11), 1853-1858(1994)   DOI   ScienceOn
15 Hargette, P., Budd, G., and Cline, M., "Strategies at Charleston CPW for compliance with DBP regulations," Proceedings of AWWA 2004 Annual Conference, June 13 -17, Orlando, Florida(2004)
16 손희종, 정철우, 강임석, '상수원중의 천연유기물질 특성과 염소 소독부산물 생성의 관계', 대한환경공학회지, 26(4), 457-466(2004)
17 Kim, J. and Reckhow, D. A., "Role of proteins and amino acids in DBP formation," Proceedings of IWA NOM Conference, September 2-4, Bath, U.K.(2008)
18 Zavaleta, J. O., Hauchman, F. S., and Cox, M. W., "Epidemiology and toxicology of disinfection by-products," Formation and Control of Disinfection By-Products in Drinking Water, Singer, P. C. (Ed), American Water Works Association, Denver, pp. 95-117(1999)
19 서인숙, 손희종, 안욱성, 유선재, 배상대, '뇨 성분에서의 염소 소독부산물 생성 특성,'대한환경공학회지, 30(3), 286-292(2008)
20 Fawell, J., Robinson, D., Bull, R., Birnbaum, L., Boorman, G., Butterworth, B., Daniel, P., Galal-Gorchev, H., Hauchman, F., Julkunen, P., Klaassen, C., Krasner, S., Orme-Zavaleta, J., Rief, J., and Tardiff, R, "Disinfection by-products in drinking water: critical issues in health effects research," Environ. Health Perspect., 105(1), (1997)
21 Ueno, H., Moto, T., Sayato, Y., and Nakamuro, K., "Disinfection by-products in the chlorination of organic nitrogen compounds: by-products from kynurenine," Chemosphere, 33(8), 1425-1433(1996).   DOI   ScienceOn
22 Armesto, X. L., Canle, M., Garcia, M. V., and Santaballa, J. A., "Aqueous chemistry of N-halo-compounds," Chemical Society Reviews, 27, 453-460(1998)   DOI   ScienceOn
23 U.S. EPA National Exposure Research Laboratory, Office of Research and Development, Method 551.1., Cincinnati, Ohio.(1995)
24 Reckhow, D. A., Rotello, V., Kim, J., and Bull, R. J., "Disinfection byproduct formation from key nitrogenous precursors," Proceedings of AWWA WQTC, (2004)
25 Krasner, S. W., "Chemistry of disinfection by-product formation," Formation and Control of Disinfection ByProducts in Drinking Water, Singer, P. C.(Ed), American Water Works Association, Denver, pp. 27-52(1999)
26 Richardson, S. D., "Disinfection by-products and other emerging contaminants in drinking water," Trends in Analytical Chemistry, 22(10), 666-684(2003)   DOI   ScienceOn
27 Reckhow, D. A., Platt, T. L., MacNeill, A L., and McClellan, J. N., "Formation and degradation of dichloroacetonitrile in drinking waters," Aqua, 50, 1-13(2001)
28 Bull, R J., Bull, M., Reckhow, D. A, "Use of quantitative structure toxicity relationships(QSTR) to identify disinfection by-products of potential health importance," Proceedings of AWWA Water Quality Technology Conference, San Antonio, U.S.A.(2004)