Simultaneous removal of ammonia and N-nitrosamine precursors from high ammonia water by zeolite and powdered activated carbon

When adding sufficient chlorine to achieve breakpoint chlorination to source water containing high concentration of ammonia during drinking water treatment, high concentrations of disinfection by-products（DBPs） may form. If N-nitrosamine precursors are present, highly toxic N-nitrosamines, primarily N-nitrosodimethylamine（NDMA）, may also form. Removing their precursors before disinfection should be a more effective way to minimize these DBPs formation. In this study, zeolites and activated carbon were examined for ammonia and N-nitrosamine precursor removal when incorporated into drinking water treatment processes.The test results indicate that Mordenite zeolite can remove ammonia and five of seven N-nitrosamine precursors efficiently by single step adsorption test. The practical applicability was evaluated by simulation of typical drinking water treatment processes using six-gang stirring system. The Mordenite zeolite was applied at the steps of lime softening, alum coagulation, and alum coagulation with powdered activated carbon（PAC） sorption. While the lime softening process resulted in poor zeolite performance, alum coagulation did not impact ammonia and N-nitrosamine precursor removal. During alum coagulation, more than67% ammonia and 70%–100% N-nitrosamine precursors were removed by Mordenite zeolite（except 3-（dimethylaminomethyl）indole（DMAI） and 4-dimethylaminoantipyrine（DMAP））. PAC effectively removed DMAI and DMAP when added during alum coagulation. A combination of the zeolite and PAC selected efficiently removed ammonia and all tested seven N-nitrosamine precursors（dimethylamine（DMA）, ethylmethylamine（EMA）, diethylamine（DEA）, dipropylamine（DPA）, trimethylamine（TMA）, DMAP, and DMAI） during the alum coagulation process.

High photocatalytic efficiency of spouting reactor compared with fluidized bed with top irradiation source

The removal of volatile organic compounds by photocatalytic degradation is one of the safest and most effective ways of removing pollutants from the air. This process is highly affected by the type of reactor, light exposure, and hydrodynamics. For scale up purposes, continuous reactors with high capacity are required for treating large amounts of feedstock. In this work, two types of reactors based on different hydrodynamics, fluidized and spouted reactors, were designed to work under light irradiation inside the reactor. The efficiency of the reactors for volatile organic compound removal from high flow rates of air under Hg lamp irradiation using N-F-TiO2 photocatalyst was investigated. The performance of the fluidized bed and spouted bed were evaluated and compared at the same weight hourly space velocity of feed stream through the reactor. The results revealed that 80% of the initial acetaldehyde was removed in the fluidized bed after about 200 min, while in the spouted bed the acetaldehyde was totally removed after about 120 min.