• Title/Summary/Keyword: Trihalomethane

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Chloroform Degradation by Water-surface Discharge (물표면 방전을 이용한 클로로포름의 분해)

  • Ryu, S.M.;Yoo, S.R.;Park, J.S.;Hong, E.J.;Lho, T.
    • Journal of Korean Society on Water Environment
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    • v.29 no.5
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    • pp.666-673
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    • 2013
  • Chloroform is harmful volatile organics and representatives of Trihalomethane (THM). Well-known removal methods of Chloroform are photo oxidation or OH radical oxidation. Plasma on water surface at slightly vacuum condition (45 torr) can produce OH radical and it will help chloroform removal. 81.5% of chloroform is removed by vacuum and plasma in 10 min.. Plasma can totally oxidize it till 2.8% and partially oxidize chloroform up to 18.5%. Water-surface plasma is good method to remove chloroform in short time.

Ozonation of Reactive Dyes and Control of THM Formation Potentials (오존산화에 의한 반응성염료의 제거 및 THM생성능의 제어)

  • 한명호;김범수;허만우
    • Textile Coloration and Finishing
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    • v.16 no.2
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    • pp.34-40
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    • 2004
  • This study was conducted to remove the reactive dyes by the Ozone demand flask method which are one of the main pollutants in dye wastewater, Ozone oxidation of three kinds of the reactive dyes was examined to investigate the reactivity of dyes with ozone, Trihalomethane formation potentials(THMFPs), competition reaction and ozone utilization on various conditions for single- and multi-solute dye solution. Concentration of dyes was decreased continuously with increasing ozone dosage in the single-solute dye solutions. THMFPs per unit dye concentration were gradually increased with increase of ozone dosage. By the result of THMFPs change with reaction time, THMFPs were rapidly decreased within 1 minute in single-solute dye solutions. Dey were increased after 1 minute of reaction time, and then they were consistently decreased again after longer reaction time. Competition quotient values were calculated to investigate the preferential oxidation of individual dyes in multi-solute dye solutions. Competition quotients$(CQ_i)$ and values of the overall utilization efficiency, no$_3$, were increased at 40mg/1 of ozone dosage in multi-solute dye solutions.

Prediction of Trihalomethane (THM) Formation By Using Ultraviolet Absorbance (자외부흡광도(紫外部吸光度)를 이용한 Trihalomethane(THM) 생성량(生成量) 예측(豫測))

  • Hwang, Yong Woo;Cho, Bong Yun;Kim, Hyung Soo
    • Journal of Korean Society of Water and Wastewater
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    • v.11 no.3
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    • pp.96-104
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    • 1997
  • In-pipe formation of THM in water distribution systems was simulated by using the continuously and easily measurable parameters such as water temperature, residual chlorine and soluble organic compounds. The concentration of miscellaneous organics which could be the precuror of THM, was measured and represented as the absorbance of ultraviolet at wave length 260 nm. As the results, the developed equation in this study showed a more reliability on the change of THM than the normally regressed equation. In addition, the simulation was successfully fitted in the actual water treatment and distribution systems. Of the THM components, dibromochloromethane was the main cause dropping the overall reliability in the simulation.

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Characterization of Dissolved Organics Based on Their Origins (상수 원수에 따른 용존 유기물의 특성 평가)

  • 허준무;박종안;장봉기;이종화
    • Journal of Environmental Science International
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    • v.8 no.3
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    • pp.337-347
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    • 1999
  • This study was carried out to evaluate the characteristics of dissolved organics based on their origins, which were divided into two categories. The first group consisted of river, lake and secondary sewage treatment effluent, which were chosen as representative of their origins. The second group were artificial samples which were made of AHA(Aldrich humic acids) and WHA(Wako humic acids). Physicochemical characteristics, biological degradability and THMEP(trihalomethane formation potential) of the samples were analysed based on the AMWD(apparent molecular weight distribution). Large portion of dissolved organic carbon(DOC) in the river and lake samples was comprised of LMW(low molecular weight), which that of AHA and WHA was HMW(high molecular weight). The DOC of the lake was evenly distributed in the all range of molecular weight. The river, lake and secondary treated effluent have lower ultraviolet(UV) absorbance at 254nm, and have a higher amount of humic acids. Higher absorbance of humic acids means that aliphatic bond and benzenoid type components that absorb UV light were contained in these kind of humic acids. It was expected that lake sample was the most biodegradable in the different samples investigated, and in order of secondary sewage treatment effluent, river, WHA and AHA based on the result of determination of specific ultraviolet absorbance(SUVA). Biodegradability showed similar result except for AHA, while dissolved organics in the range of LMW decreased during the biodegradability test, and on the contrary those of HMW increased. Production of the SMPs(soluble micobial products) was observed during humicfication of dissolved organics and the SMPs were higher production of the SMPs. THM formation was high in the samples containing HMW and similar tendency was shown in the THMEP(trihalomethane formation potential), except for WHA.

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Formation Characteristics of DBPs by Chlorination in Water Treatment Plant (정수장에서 소독부산물의 생성특성)

  • Rhee, Dong-Seok;Min, Byoung-Seob;Park, Sun-Ku;Kim, Joung-Hwa;Rhyu, Jae-Keun
    • Journal of Korean Society on Water Environment
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    • v.20 no.1
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    • pp.55-62
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    • 2004
  • This study was carried out to investigate the formation of DBPs(Disinfection By-products) such as trihalomethane(THMs) and haloacetic acid(HAAs) by chlorination in raw water and finished water of Water Treatment Plant(WTP). The formation of THMs was increased with the increase of pH and reaction time. HAAs was found as a high formation at a pH 7 and low formation at pH 9. THMFP(Trihalomethane Formation Potential) was the highest formation potential in raw water of Pu-1 and the lowest in raw water of Pa-1. In case of HAAFP(Haloacetic acid formation potential), So-1 showed the highest value, while Pa-1 showed the lowest value. It was investigated the relationship between HAAs and organic matters which were described as DOC(dissolved organic carbon) and $UV_{254}$. In both DOC and $UV_{254}$ versus HAAFP, Pu-1 showed the good correlation coefficients($r^2$) with 0.95 and 0.84, respectively. For three WTP investigated, DBPs(THMs + HAAs) was shown over the range of $42.00{\sim}49.36{\mu}g/L$. This result might be due to the different characteristic of organic matters in raw water and the difference of chlorine dosage for a water treatment.

Removal of natural organic matter and trihalomethane formation potential by four different coagulants during coagulation-microfiltration processes (응집과 막여과 공정에서 응집제에 따른 유기물 및 THMFP제거)

  • Park, Keun Young;Choi, Yang Hun;Jin, Yong Chul;Kang, Sun Ku;Kweon, Ji Hyang
    • Journal of Korean Society of Water and Wastewater
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    • v.27 no.1
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    • pp.101-112
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    • 2013
  • Integrated process with coagulation and microfiltration as an advanced water treatment has been expanded its application in recent years due to its superb removal of particles and natural organic matter. In usual, effectiveness of coagulation sometimes determines performance of the whole system. Several new polymeric coagulants introduced to water utilities for better efficiency were studied in this paper. Three polymeric coagulants (i.e., PACl, PACs, and PAHCs) along with alum were evaluated for removal of natural organic matter, especially for reduction of trihalomethane formation potential, for which regulation has become stringent. Turbidity removal was closely related to pH variation showing the reduced turbidity removal by PACs due to the decreases in the pH of supernants at high doses. The four coagulants showed different organic matter removal during coagulation and affected the removal in microfiltration. For instance, DOC concentration was not reduced by microfiltration when PAHCs were used however 10 % of DOC removal was observed by microfiltration with alum coagulation. Coagulation pretreatment also impacted the THM removals, i.e., approximately 30 % of THMs and 13 % of DOC was removed by microfiltration only, but 40 to 67 % of THMs and 30 % of DOC was removed by the integrated process. Strategies on selection of coagulants are needed depending on characteristics of target pollutants in raw waters.

Determination of THM(trihalomethane) in Rain by using Solid Phase Micro-Elctraction(SPME) Fiber Assembly (고상 미량 추출 장치(SPME, solid phase micro-extraction device)를 이용한 물 중의 THM(trihalomethane) 분석)

  • 유광식;박상윤
    • Journal of Environmental Science International
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    • v.6 no.3
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    • pp.277-283
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    • 1997
  • SPME deuce was applied to determine the THM in an aqueous solution. The 6 kinds of THM was quantitatively detenuned by using GC-ECD which has the sample eutracted on the SPME fiber from an aqueous solution for 10 min. The THM components were well separated from $CHCl_3$ to the last $CHBr_3$ UHh 13 mons at the condition. 6 kinds of the volatile halogenated organic compounds: $CHCl_3$, $CHBrCl_2$, $CHBrtCl_2$, $CHCl_3$, $C_2Cl$. and $CHBr_3$, showed well defirled calibration graph with good llnearlty from a few ppb level up to several tens of pub concentration. $CHBr_2Cl$ and $C_2C1_4$ were detected from a few samples among the 10 of river samples. CHCl3, however, was detected In 4 sea water samples with the highest of 10 ppd among the pouuted 6 positions. Trace level of $CHBr_2Cl$ and few pub level of $CHBr_3$ were also detected at the other two sample stations. Most of the 13 rain water samples collected from 6 sampling stations were contained ppd level of $CHCl_3$, and also $CHBr_2Cl$, and C_2Cl_4$ were only detected at trace level at a few rain samples among them. We could recognize the fact that our Ut and water enoronment has already been contaminated by certain volatile halogenated organic compounds through this study.

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A Study on Evaluation of Adsorption Performance of Humic Acid on Granular Activated Carbon (Humic acid 제거를 위한 국산 입상활성탄의 흡착성능 평가에 관한 연구)

  • Shin, Sung-Gyo;Kim, Jong-Gu;Park, Cheong-Gil
    • Journal of Environmental Science International
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    • v.2 no.1
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    • pp.73-81
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    • 1993
  • Adsorption process using granular activated carbon(GAC) has been considered as one of the most effective water treatment technologies to remove humic acid which is recon- niEed as trihalomethane(THM) precursor in chlorination. To design the most effective GAC process, it is necessary to conduct the test of adsor- ption performance by means of isothem, batch rate and column studies and to select the most effective activated carbon according to raw materials of GAC - lignite and coconut shell. The objective of this study is to investigate the adsorption performance of humid acid on two activated carbons - lignite activated carbon(LAC) and coconut shell activated car- bon(CAC) made in Korea. It is available to represent UV-abs and trihalomethane formation potential(THMFP) as concentration of humic acid due to good relationship. The adsorption capacity of humid acid is not concerned with surface area of activated carbon but with pore size related to about $100{\AA}$, and then LAC forming at the extent of mesopore is found to be eight times more effective in adsorption capacity than CAC forming at micropore. The adsorption capacity of LAC and CAC is better at pH 5.5 than at pH 7. Pore and surface diffusion coefficients calculated from the diffusion model are $7.61\times10^{-13}m^2/sec$, $3.52\times10^{-15}m^2/sec$ for CAC, and $3.38\times10^{-12}m^2$/sec and $Ds=1.48{\times}10^{-15}m^2/sec$ for GAC respectively. From the results of column test it shows that the performance of LAC is also better than CAC and the optimal EBCT(Empty Bed Contact Time) is 4.52min. and activated carbon removes selectively the components of humic acid to be easily formed to THM.

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