Loading…

Effect of oxoanions on oxidant decay, bromate and brominated disinfection by-product formation during chlorination in the presence of copper corrosion products

The present study investigated the effect of oxoanions on catalytic behaviour of copper corrosion products (CCPs) during chlorination of bromide-containing waters. Three types of oxoanions (carbonate, sulphate, and phosphate) and four types of CCPs (Cu2+, Cu(OH)2, Cu2O, and CuO) were involved in inv...

Full description

Saved in:
Bibliographic Details
Published in:Water research (Oxford) 2019-12, Vol.166, p.115087-115087, Article 115087
Main Authors: Fang, Chao, Ding, Shunke, Gai, Shibo, Xiao, Rong, Wu, Yinan, Geng, Bing, Chu, Wenhai
Format: Article
Language:English
Subjects:
Citations: Items that this one cites
Items that cite this one
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
Description
Summary:The present study investigated the effect of oxoanions on catalytic behaviour of copper corrosion products (CCPs) during chlorination of bromide-containing waters. Three types of oxoanions (carbonate, sulphate, and phosphate) and four types of CCPs (Cu2+, Cu(OH)2, Cu2O, and CuO) were involved in investigation and the effect of oxoanions concentration was also examined. The result indicated that carbonate and sulphate slightly inhibited oxidant decay in the presence of CCPs, but the formation of brominated disinfection by-products (Br-DBPs) remained largely unchanged. In contrast, the presence of phosphate (0.2–1 mM) almost eliminated the catalytic effect of Cu2+. For CCP solids (i.e. Cu(OH)2, Cu2O, and CuO), phosphate preferentially inhibited the formation of bromate rather than Br-DBPs. Despite the catalysis by CCP solids was reduced to some extent, the oxidant decay rate and bromate and Br-DBP formation were still significantly higher than blank groups, even at high phosphate concentration. By testing different addition scheme (simultaneous/sequential addition), it was proposed that phosphate was a strong competitor for hypohalites, rapidly destroying CCPs-hypohalites complexes on some adsorption sites. However, there were some specific sites that can only be adsorbed by hypohalites, leading to the incomplete inhibition of phosphate. Finally, the inhibition effect of phosphate on CCPs catalysis was tested in real water matrix. For Cu2+, higher reduction of bromate and Br-DBPs was found in raw water rather than filtered water, while converse pattern was true for Cu(OH)2 and Cu2O, and this discrepancy can be ascribed to the difference in catalytic mechanism between Cu2+ and CCP solids. [Display omitted] •CCPs-catalysed oxidant decay and Br-DBP formation was strongly inhibited by phosphate.•Carbonate and sulphate exhibited less effect on catalytic behaviour of CCPs than phosphate.•Phosphate preferentially suppressed the formation of bromate rather than that of Br-DBPs.•Competitive mechanism between oxoanions and hypohalites was proposed.•The inhibition effect of phosphate was verified in real waters.
ISSN:0043-1354
1879-2448
DOI:10.1016/j.watres.2019.115087