Combined Ozone and Ultrasound for the Removal of 1,4-Dioxane from Drinking Water

被引:17
|
作者
Dietrich, Michael [1 ,2 ]
Andaluri, Gangadhar [1 ]
Smith, Ryan C. [1 ,2 ]
Suri, Rominder [1 ,2 ]
机构
[1] Temple Univ, Dept Civil & Environm Engn, 1947 N 12th St, Philadelphia, PA 19122 USA
[2] Temple Univ, NSF Water & Environm Technol WET Ctr, Civil & Environm Engn, Philadelphia, PA 19122 USA
关键词
Ozone; 1; 4-Dioxane; AOP; Pressurized Reactor; Ultrasound; OPERATIONAL CONDITIONS; OZONATION PROCESSES; HYDROGEN-PEROXIDE; AQUEOUS-SOLUTION; DEGRADATION; OXIDATION; DECOMPOSITION; KINETICS; MECHANISM; BIODEGRADATION;
D O I
10.1080/01919512.2017.1321981
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Ozone, ultrasound, and ozone/ultrasound processes were evaluated for the removal of 1,4-dioxane from tap water using a continuous flow reactor with on-line aqueous ozone measurement. The addition of ultrasound to ozone was found to significantly boost removal. The removal of 1,4-dioxane by ozone/ultrasound process exceeded the sum of the removals from ozone alone and ultrasound alone. Ultrasound alone showed less than 20% removal of 1,4-dioxane. The effects of reactor pressurization and bicarbonate as a hydroxyl radical scavenger were also studied. It was observed that at constant aqueous ozone concentration, additional pressure in the reactor tended to mute the 1,4-dioxane removal boost noted in the ozone/ultrasound process, while additional pressure did not affect 1,4-dioxane removal via ozone alone. The removal of 1,4-dioxane was found to be dependent on the consumption of aqueous ozone, and the consumption of ozone was found to be increased by either the addition of ultrasound or by increasing pH. Rate constants were calculated for various ozone concentrations for the ozone and ozone/ultrasound processes and the systems were fitted to a Chick-Watson model.
引用
收藏
页码:244 / 254
页数:11
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