Formation of assimilable organic carbon (AOC) and specific natural organic matter (NOM) fractions during ozonation of phytoplankton

被引:118
作者
Hammes, Frederik
Meylan, Sebastien
Salhi, Elisabeth
Koester, Oliver
Egli, Thomas
Von Gunten, Urs
机构
[1] Swiss Fed Inst Aquat Sci & Technol, CH-8600 Dubendorf, Switzerland
[2] WVZ, CH-8023 Zurich, Switzerland
[3] ETH, Inst Biogeochem & Pollutant Dynam, CH-8092 Zurich, Switzerland
关键词
assimilable organic carbon (AOC); biological stability; drinking water; natural organic matter (NOM); phytoplankton; ozone;
D O I
10.1016/j.watres.2007.01.001
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Ozonation of natural surface water increases the concentration of oxygen-containing low molecular weight compounds. Many of these compounds support microbiological growth and as such are termed assimilable organic carbon (AOC). Phytoplankton can contribute substantially to the organic carbon load when surface water is used as source for drinking water treatment. We have investigated dissolved organic carbon (DOC) formation from the ozonation of a pure culture of Scenedesmus vacuolatus under defined laboratory conditions, using a combination of DOC fractionation, analysis of selected organic acids, aldehydes and ketones, and an AOC bioassay. Ozonation of algae caused a substantial increase in the concentration of DOC and AOC, notably nearly instantaneously upon exposure to ozone. As a result of ozone exposure the algal cells shrunk, without disintegrating entirely, suggesting that DOC from the cell cytoplasm leaked through compromised cell membranes. We have further illustrated that the specific composition of newly formed AOC (as concentration of organic acids, aldehydes and ketones) in ozonated lake water differed in the presence and absence of additional algal biomass. It is therefore conceivable that strategies for the removal of phytoplankton before pre-ozonation should be considered during the design of drinking water treatment installations, particularly when surface water is used. (c) 2007 Elsevier Ltd. All rights reserved.
引用
收藏
页码:1447 / 1454
页数:8
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