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Study On The Control Effect Of Combined Process On The Precursors Of Disinfection Byproduct In Surface Water

Posted on:2021-01-07Degree:MasterType:Thesis
Country:ChinaCandidate:B M LiuFull Text:PDF
GTID:2392330611473181Subject:Environmental Science and Engineering
Abstract/Summary:PDF Full Text Request
Disinfection is one of the important processes before drinking water enters the pipe network,which can effectively avoid the growth of microorganisms to ensure the biosecurity of the drinking water.However,the disinfection process is inevitably to cause the formation of poisonous and harmful disinfection byproducts?DBPs?,which will pose the potential threat for the using and drinking of water.Hence,it is of great significance to explore the characteristics of DBP precursors as well as DBPs formation mechanism,and further establish an effective advance treatment process to control the DBPs contained in drinking water.In this study,the typical DBP precursors in the surface water was identified and characterized,their DBPs formation mechanisms were also explored after chlorination.The O3-ceramic membrane filtration?O3-CMF?and O3-biological activated carbon?O3-BAC?processes were further established for DBPs precursors'removal.The removal effect and mechanism of typical DBPs precursors in surface water advance treatment was further investigated.The main research contents and conclusions were shown as follows.?1?The characteristics of DBP precursors and DBPs formation mechanism in surface water were evaluated,and their control effect by the conventional process was also evaluated.Results indicated that the DBP precursors in raw water mainly included aromatic proteins-like,fulvic acids-like,soluble microbial products and analogues?SMPs-like?as well as humic acids-like,etc.After chlorination,high concentration of carbonaceous disinfection byproducts?C-DBPs?was detected,which primarily consist of trihalomethanes?THMs?and halogenated acetic acids?HAAs?.In addition,THMs had obviously higher formation content in the water during spring and winter,which accounted for 66.76%and 63.94%of the measured total C-DBPs,respectively.And HAAs showed much higher formation content in the water during summer and autumn,which accounted for 42.95%and 51.99%of the measured total C-DBPs,respectively.Compared with C-DBPs,the formation of nitrogenous DBPs?N-DBPs?was much lower than that of raw water.Haloacetonitriles?HANs?was the mainly component of measured N-DBPs,indicating the high production of 34.31?g·L-1?in summer?and 44.38?g·L-1?in autumn?.Trihalonitromethanes?THNMs?showed a much lower contribution to the total N-DBPs formation,with the highest production of 7.33?g·L-1 in spring.Pearson correlation analysis indicated that the formations of THMs,chloral hydrate?CH?,haloketones?HKs?and THNMs during raw water chlorination were significantly relevant with the humic acid-like substances in the raw water,with the correlation coefficient?R2?of 0.88,0.71,0.66 and 0.85,respectively.The formations of HAAs and HANs showed obvious correlation with the SMPs?R2=0.86?and aromatic protein-like components?R2=0.78?in the raw water,recpectively.Conventional processes of drinking water treatment had low removal efficiency for DBPs precursors,resulting in a decrease of 20.43%and 22.45%for C-DBPs and N-DBPs in the effluent respectively.?2?Because of the poor removal efficiency of DBP precursors by conventional processes,the O3-CMF process was constructed to advanced treat the effluent of conventional processes,the mechanism of different O3-CMF coupling methods and the removal effect of O3-CMF on DBPs were investigated synthetically,in this study.Compared with the influent?conventional process effluent?,the ex-situ O3-CMF led to a decrease of 21.86%in C-DBPs formation and16.19%in N-DBPs formation respectively,while the in-situ O3-CMF resulted in a decrease of32.35%in C-DBPs formation and 19.13%in N-DBPs formation respectively.Results indicated that the in-situ O3-CMF was more effective for DBP precursors control than ex-situ O3-CMF.This might be due to the catalytic ozonation induced by ceramic membrane pores,which led to the decomposition of O3 and produce more hydroxyl radicals?·OH?.Under the synergistic effect of O3,·OH oxidation,and ceramic membrane retention,O3-CMF could effectively reduce the total fluorescence response intensity and high molecular weight?the relative molecular mass>0.3×103?organic matters,resulting in the decrease of total DBPs formation.However,the oxidation of O3 and·OH would lead to the formation of low molecular organic compounds which were ineffectively retained by the ceramic membrane,increasing HKs,CH and THNMs formation.In addition,increasing the concentration of O3 was difficult to enhance the removal of DBP precursors by O3-CMF.When the O3 concentration increased from 0.5 mg·L-1 to 4.0mg·L-1,the removal rate of ex-situ O3-CMF to the total DBP precursor increased from 14.03%to 25.72%,and in-situ O3-CMF removal rate of total DBP precursors increased from 25.19%to27.81%.?3?O3-BAC process was further applied to advanced treat the conventional process effluent.The effect of operating parameters such as empty bed contact time?EBCT?and O3concentration on the removal of DBPs and their precursors was also investigated.The results showed that the removal of DBP precursors by O3-BAC process was better than O3-CMF,which displayed a decrease of 30.49%in C-DBPs formation and 42.09%in N-DBPs formation respectively.Extending EBCT was in favor of the degradation of aromatic-like proteins and SMPs-like organics by microorganisms,thereby reducing the formation of total DBPs.However,further increase of EBCT had no obvious effect on DBP precursors removal.When EBCT was increased from 20 min to 30 min,the remove efficiency of O3-BAC for C-DBPs and N-DBPs only increased 1.63%and 1.04%,respectively.Furthermore,the removal rate of C-DBPs increased from 20.64%to 56.05%and N-DBPs increased from 18.58%to 61.89%respectively,when the concentration of O3 addition increased from 0 mg·L-1 to 2.0 mg·L-1.This was mainly attributed to the fact that O3 oxidized the refractory organic matter in raw water into biodegradable substances,which enhanced the biodegradation of BAC with the microbial activity of 62.52%.However,when the O3 concentration was further increased to 4.0 mg·L-1,the microbial survival rate decreased to 49.9%,further led to the release of Intracellular organic matter such as protein and SMPs.Those newly produced DBP precursors would result in an increased formation of C-DBPs and N-DBPs by 12.63%and 18.72%,respectively.In summary,an appropriate dosage of O3 was beneficial for removing DOM by O3-BAC,but excessive O3concentration caused the formation of new DBP precursors.
Keywords/Search Tags:surface water, dissolved organic matter, ozone-ceramic membrane, ozone-biological activated carbon, disinfection byproducts
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