Formation of N-nitrosodimethylamine (NDMA) from reaction of monochloramine:: a new disinfection by-product

被引:366
作者
Choi, JH [1 ]
Valentine, RL [1 ]
机构
[1] Univ Iowa, Dept Civil & Environm Engn, Iowa City, IA 52242 USA
关键词
disinfection by-product (DBP); N-nitrosodimethylamine (NDMA); monochloramine; 1,1-dimethyihydrazine (UDMH); chlorine transfer;
D O I
10.1016/S0043-1354(01)00303-7
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Studies have been conducted specifically to investigate the hypothesis that N-nitrosodimethylamine (NDMA) can be produced by reactions involving monochloramine. Experiments were conducted using dimethylamine (DMA) as a model precursor. NDMA was formed from the reaction between DMA and monochloramine indicating that it should be considered a potential disinfection by-product. The formation of NDMA increased with increased monochloramine concentration and showed maximum in yield when DMA was varied at fixed monochloramine concentrations. The mass spectra of the NDMA formed from DMA and N-15 isotope labeled monochloramine ((NH2Cl)-N-15) showed that the source of one of the nitrogen atoms in the nitroso group in NDMA was from monochloramine. Addition of 0.05 and 0.5 mM of preformed monochloramine to a secondarily treated wastewater at pH 7.2 also resulted in the formation of 3.6 and 111 ng/L of NDMA, respectively, showing that this is indeed an environmentally relevant NDMA formation pathway. The proposed NDMA formation mechanism consists of (i) the formation of 1,1-dimethylhydrazine (UDMH) intermediate from the reaction of DMA with monochloramine followed by, (ii) the oxidation of UDMH by monochloramine to NDMA, and (iii) the reversible chlorine transfer reaction between monochloramine and DMA which is parallel to (i). We conclude that reactions involving monochloramine in addition to classical nitrosation reactions are potentially important pathways for NDMA formation. (C) 2002 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:817 / 824
页数:8
相关论文
共 33 条
[1]  
*APHA AWWA WEF, 1992, STAND METH EX WAT WA
[2]   FORMATION OF HYDRAZINE FROM TERT-BUTYL HYPOCHLORITE AND AMMONIA [J].
AUDRIETH, LF ;
COLTON, E ;
JONES, MM .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1954, 76 (05) :1428-1431
[3]   TRANSFORMATIONS OF METHYLAMINES AND FORMATION OF A HAZARDOUS PRODUCT, DIMETHYLNITROSAMINE, IN SAMPLES OF TREATED SEWAGE AND LAKE WATER [J].
AYANABA, A ;
ALEXANDER, M .
JOURNAL OF ENVIRONMENTAL QUALITY, 1974, 3 (01) :83-89
[4]  
Borstel R.C.V., 1984, IARC SCI PUBLICATION, V57
[5]   THE RASCHIG SYNTHESIS OF HYDRAZINE [J].
CAHN, JW ;
POWELL, RE .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1954, 76 (09) :2565-2567
[6]  
*CAL DEP HLTH SERV, 2000, CAL DRINK WAT NDMA R
[7]  
CASTEGNARO M, 1986, AM IND HYG ASSOC J, V47, P360, DOI 10.1202/0002-8894(1986)047<0360:ODOHPN>2.3.CO
[8]  
2
[9]   RAPID FORMATION OF CARCINOGENIC N-NITROSAMINES IN AQUEOUS ALKALINE-SOLUTIONS [J].
CHALLIS, BC ;
KYRTOPOULOS, SA .
BRITISH JOURNAL OF CANCER, 1977, 35 (05) :693-696
[10]   CHLORINE TRANSFER FROM CHLORAMINE TO AMINES IN AQUEOUS-MEDIUM .1. REACTION BETWEEN CHLORAMINE AND METHYLAMINE [J].
FERRIOL, M ;
GAZET, J ;
RIZKOUAINI, R ;
ADAD, MTS .
INORGANIC CHEMISTRY, 1989, 28 (20) :3808-3813