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Removal of precursors of chlorinated organic compounds in selected water treatment processes

机译:在选定的水处理过程中去除氯化有机物的前体

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This paper discusses the impact of coagulation, ozonation and adsorption on the activated carbon, the content of precursors of chlorinated organic compounds. Coagulation guaranteed the effective elimination of non-biodegradable organic substances and essentially did not impact the biodegradable dissolvent organic carbon (DOC) concentrations. The coagulation process brought about a decrease in concentration for all analysed fractions of organic substances. The removal efficiency of organic substances was higher for mixed water than surface water (SW). Conversely ozonation lowered the biological stability of water by increasing the biodegradable DOC concentration, while only marginally causing the mineralisation of refractive substances. The non-biodegradable organic substances' mineralisation level for the water samples was between 0.00-1.35 gC/m~3 (for SW) and 0.02-0.46 gC/m~3 (for infiltration water). In general, a higher mineralisation level was registered for SW. Adsorption, despite its substantial removal effectiveness, did not cause the total elimination of high-molecular weight organic substances. In general, total and dissolved organic carbon was more effectively eliminated from SW, probably due to higher pre-adsorption concentration levels in SW. All analysed processes decrease the potential to create chlorinated organic substances through a disinfection process.
机译:本文讨论了混凝,臭氧化和吸附对活性炭,氯化有机物前体含量的影响。混凝可确保有效消除不可生物降解的有机物质,并且基本上不会影响可生物降解的可溶性有机碳(DOC)的浓度。凝结过程导致所有分析的有机物组分浓度降低。对于混合水,有机物质的去除效率要比地表水(SW)高。相反,臭氧化通过增加可生物降解的DOC浓度而降低了水的生物稳定性,而仅少量地引起折射物质的矿化。水样品中不可生物降解的有机物的矿化度在0.00-1.35 gC / m〜3(对于西南水)和0.02-0.46 gC / m〜3(对于渗入水)之间。一般而言,西南部的矿化度较高。尽管吸附具有相当大的去除效果,但它并未完全消除高分子量有机物。通常,总有机碳和溶解有机碳可以更有效地从SW中消除,这可能是由于SW中较高的预吸附浓度水平所致。所有经过分析的过程都减少了通过消毒过程产生氯化有机物的可能性。

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