Factors controlling nitrosamine formation during wastewater chlorination

2002 ◽  
Vol 2 (3) ◽  
pp. 191-198 ◽  
Author(s):  
W.A. Mitch ◽  
D.L. Sedlak

Recent discoveries of the formation of low levels of the potent carcinogen N-nitrosodimethylamine (NDMA) during wastewater chlorination has caused concern where indirect potable water reuse is practiced. Experiments indicate that nitrosamine formation during chlorination of wastewater is consistent with a reaction scheme involving the slow formation of a hydrazine intermediate from a secondary amine and monochloramine, followed by its rapid oxidation to the corresponding N-nitrosamine. A survey of precursors indicates that secondary amines form their corresponding N-nitrosamines to the greatest extent. However, molecules containing the secondary amine as a functional group can also form the corresponding N-nitrosamine. NDMA is the predominant N-nitrosamine found in chlorinated wastewater. However, other nitrosamines are detected. These N-nitrosamines may be important if the summed risk posed by the exposure to all N-nitrosamines is considered.

1998 ◽  
Vol 38 (6) ◽  
pp. 1-8 ◽  
Author(s):  
Charles N. Haas ◽  
R. Rhodes Trussell

The development of potable water reuse systems (systems for the treatment of wastewater to quality adequate to augment other surface water supplies) requires careful attention to the consistent production of product water which has low levels of contaminants, such as infectious pathogens, capable of causing human health effects from acute exposure. Little consideration has been given to the formal specification of the degree of reliability of such systems. In this paper we present two ways to approach the problem. The first is a formal extension of the ‘multiple barrier’ concept often cited in the water treatment literature. The second is an application of probabilistic analysis. With either method, it is clear that much more information should be obtained with respect to the failure modes, and the frequency with which individual processes achieve a particular level of performance. However the conceptual framework presented here should enable a formal analysis of the problem to be conducted.


2021 ◽  
Author(s):  
Qingmin Wang ◽  
Xiaochen Wang ◽  
Binbing Zhu ◽  
Jianyang Dong ◽  
hao tian ◽  
...  

The widespread presence of secondary amines in agrochemicals, pharmaceuticals, natural products, and small-molecule biological probes has inspired efforts to streamline the synthesis of molecules with this functional group. Herein, we...


2017 ◽  
Vol 16 ◽  
pp. 581-605 ◽  
Author(s):  
Stuart J. Khan ◽  
Troy Walker ◽  
Benjamin D Stanford ◽  
Jörg E. Drewes

2021 ◽  
Author(s):  
Cara Lucas ◽  
Barbara Johnson ◽  
Elizabeth Hodges Snyder ◽  
Srijan Aggarwal ◽  
Aaron Dotson

2005 ◽  
Vol 2005 (10) ◽  
pp. 5577-5590
Author(s):  
Loretta Mokry ◽  
Darrel Andrews ◽  
Woody Frossard ◽  
Mark Perkins ◽  
Alan H. Plummer

2017 ◽  
Vol 125 ◽  
pp. 42-51 ◽  
Author(s):  
Hui Wang ◽  
Minkyu Park ◽  
Heng Liang ◽  
Shimin Wu ◽  
Israel J. Lopez ◽  
...  

2018 ◽  
Vol 73 (1) ◽  
pp. 43-74 ◽  
Author(s):  
Cindy Döring ◽  
Peter G. Jones

AbstractThe reaction of (tht)AuX (X=Cl or Br; tht=tetrahydrothiophene) with various primary amines L leads to products of the form [L2Au]+X−. Packing diagrams of the corresponding structures are dominated by N–H···X hydrogen bonds and (in some cases) aurophilic contacts. The cyclohexylamine derivative was already known as its dichloromethane ⅔-solvate; we have isolated the solvent-free compound and its pentane ¼-solvate, which all show different packing patterns. With acyclic secondary amines, the products are more varied; LAuX and [L2Au]+[AuX2]− were also found. These gold(I) products were generally formed in satisfactory quantities. The attempted oxidation to Au(III) derivatives with PhICl2 or Br2 proved impossible for the primary amine derivatives [although isopropylamine-trichloridogold(III) was obtained unexpectedly from the corresponding cyanide] and unsatisfactory for the secondary amine derivatives. Products LAuX3 and [L2AuX2]+[AuX4]− were identified but were formed in disappointing yields. In isolated cases protonated products (LH)+[AuCl4]−, (LH+)3[AuCl4]−(Cl−)2 or [(Et2N)2CH]+[AuBr4]− were formed, presumably by involvement of the dichloromethane solvent and/or adventitious water. Here also the yields were poor, and some products arose as mixtures. Direct reaction of amines with AuCl3 or (tht)AuX3 was also unsuccessful. All products were characterized by X-ray structure analysis.


Author(s):  
Cecilia Tortajada ◽  
John C. Radcliffe
Keyword(s):  

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