• Title/Summary/Keyword: Bromine substituents

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A Survey of THMs Formation in J Water Purification Plant and Its Reduction by PAC Treatment during Summer (J 정수장의 하절기 THMs 생성현황과 분말활성탄 처리에 의한 저감효과)

  • Hwang, Gap-Soo;Lee, Jang-Hoon
    • Journal of Environmental Health Sciences
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    • v.25 no.3
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    • pp.1-6
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    • 1999
  • This study was conducted to survey trihalomethane(THMs) levels in finished water of J water treatment plant and examine its reduction by powder activated carbon(PAC) treatment. Samples were collected weekly based and head-space technique was employed to determine THMs levels by G.C-ECD. THMs levels in finished waters were highest in August and showed close relationship with water temperature. All the samples satisfied the drinking water limit(100 ${\mu}$g/l) for THMs. The individual formation rates of THMs were 64.8% for CHCl$_3$, 28.4% for CHCl$_2$BR, 6.5% for CHClBr$_2$ and 0.3% for CHBr$_3$, respectively and showed little monthly difference. The reduction efficiency of THMs formation by PAC treatment was 67% during July and August. Bromine substituents were more efficiently reduced than CHCl$_3$ by PAC.

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The Effect of Substituent, Pressure and Temperature on the Dissociation Constants of Organic Acids. (2) Dissociation Constants of Some Substituted Naphthols in Aqueous Solution (유기산의 해리평형에 미치는 치환기 효과와 그의 온도 및 압력의 영향. (2) 수용액중에서 몇가지 치환나프톨류의 해리상수)

  • Jung-Ui Hwang;Zun-Ung Bae;Jong-Jae Chung;Jae-Won Jung;Kyung-Hee Chang
    • Journal of the Korean Chemical Society
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    • v.30 no.2
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    • pp.152-158
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    • 1986
  • The dissociation constants of 4-Cl-1-naphthol, 6-Br-2-naphthol and $8-NH_2-2-naphthol$ in aqueous solution were measured by spectroscopic method in the temperature range from 25 to 40${\circ}C$ and pressure up to 2000bar. The dissociation constants were decreased as the substituents were inserted in naphthol f rom $4.4{\times}10^{-10}\;to\;5.82{\times}10^{-11}$ as chloride compound and $2.5{\times}10^{-10}\;to\;3.44{\times}10^{-11}\;or\;4.21{\times}10^{-11}$ as bromine or amino compounds, respectively. This decrease can be explained with the I-or R-effects of substituents. From the dissociation constants various thermodynamic properties were calculated and discussed the characteristics of the dissociation reaction.

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