• Title/Summary/Keyword: 염소계화합물

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고무상 고분자막을 통한 물에 용해된 미량의 유기 염소계 탄화수소화합물의 분리

  • 오부근;하성룡;하상태;이영무
    • Proceedings of the Membrane Society of Korea Conference
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    • 1993.10a
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    • pp.54-55
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    • 1993
  • 유기염소계 화합물들은 저렴한 가격과 우수한 세정력으로 기계, 금속, 섬유산업에서 뿐만아니라 일반적인 용제로도 널리 사용되고 있다. 그러나, 현재 산업현장에서사용 후 처리에 있어 유기염소계 화합물들을 완전히 제거하지 못하고 방출하는 실정이다. 또한, 음용수제조시 행해지는 염소소득으로 미량의 트리할로메탄(THM)인 클로로포름이 생성된다. 이러한 유기염소계 화합물들은 음용수 중에 포함되어 체내로 흡수되면 암을 유발시킨다. 따라서 물중에 용해된 미량의 유기염소계 화합물들을 제거하는 것이 필수불가결한 실정이다.

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광양만내 유기염소계화합물의 오염

  • 홍상희;임운혁;심원준;오재룡
    • Proceedings of the Korea Society of Environmental Biology Conference
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    • 2002.11a
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    • pp.15-24
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    • 2002
  • Polychloinated biphenyls (PCBs) 및 유기염소계 농약은 UNEP에서 지속성유기오염물질(POPs)로 규정하고 있는 화합물로서 환경내 잔류성이 강하고 먹이사슬을 딸라 생물증폭되는 화합물로 알려지고 있다. 광양만의 유기염소계화합물의 오염현황을 파악하고자, 표층퇴적물, 생물, 해수 중의 농도를 정량ㆍ정성분석하였다. 해수의 용존상을 제외한 모든 매질에서 PCBs와 DDT 화합물이 주요 유기염소계 화합물로 검출되었다. 퇴적물 중의 총 PCBs, DDTs, CHLs(클로르단 화합물), HCHs (헥사클로르사이클로헥산)의 농도는 각 각 0.61-1.97 ng/g, 0.16-1.16 ng/g, nd-0.51 ng/g, 0.05-0.79 ng/g의 농도 범위를 나타냈다. 퇴적물 중의 유기염소계화합물의 농도수준은 우리나라 주요 만 (부산만, 영일만, 울산만, 경기만)에서 조사된 퇴적물 중의 농도와 비교할 때 낮은 수준이며, 저서생물에 독성학적 위해를 일으킬 수 있는 수준에 미치지 못한다. 이매패류 중의 유기염소계화합물의 농도는 총 PCBs (4.42-19.ng/g), 총 BBTs (7.54-22.6ng/g), CHLs (0.49-2.0ng/g), HCHs (0.82-7.32ng/g)의 범위를 나타었다. PCBs의 경우 산업시설 및 도시 주변에서 상대적으로 높았으나 전반적으로 비슷한 수준을 나타냈다. 해수 중의 PCBs 농도는 제철소 인근에서 상대적으로 높았으며, 해수의 용존상에서는 입자상에서와 달리 DDTs보다 HCHs가 상대적으로 높은 농도로 검출되었다. 이는 두 상에 분배되는 이들 화합물의 성향에 따르는 것으로 파악된다.

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Manganese Oxide Catalyzed Fenton-like Reduction of Chlorinated Compounds (산화망간으로 촉매화된 펜톤유사반응을 적용한 염소계화합물의 환원분해)

  • 김상민;공성호;김용수
    • Journal of Soil and Groundwater Environment
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    • v.7 no.3
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    • pp.95-102
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    • 2002
  • Manganese oxide/ hydrogen peroxide($MnO_2$/${H_2}{O_2}$) reactions were investigated as an alternative to Fenton-like reaction to reduce chlorinated organic compounds in groundwater This system showed high degradation of CT with low ${H_2}{O_2}$concentration($\leq$294mM) at neutral condition, and CT degradation increased with increasing pH values. The rate of CT degradation was not so much dependent on increase in $MnO_2$concentration since increase in production of oxygen during the reaction obstructed reaction of ${H_2}{O_2}$ on the surface of $MnO_2$. These results show that $MnO_2$catalyzed Ponton-like reaction could be a potential alternative method for treating chlorinated organic compounds in groundwater.

Environmental Occurrence of Persistent Organochlorines in Gwangyang Bay (광양만내 지속성유기염소계화합물의 잔류농도 및 분포특성)

  • 홍상희;임운혁;심원준;오재룡
    • Korean Journal of Environmental Biology
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    • v.22
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    • pp.30-37
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    • 2004
  • Peysistent oyganochlorine compounds (OCs) weve determined in sediments and bivalves from Gwangyang Bay. The concentrations of ∑PCB, ∑DDT, ∑HCH and ∑CHL in sediments were in the range of f 2.25∼11.4 ng g$\^$-1/, 0.16∼1.16 ng g$\^$-1/, nd∼0.51 ng g$\^$-1/, and 0.05∼0.79 ng g$\^$-1/, respectively. The overall OCs concentrations in sediments were below the effect range -median (ER-M) values toy benthic organisms suggested by NOAA (1991). Levels of PCB compounds a re relatively lower than other industrialized bays (Pusan Bay, Ulsan Bay, and Youngil Bay). OCs accumulated in bivalves were higher than those in sediments. In bivalves, the concentration ranges of ∑PCB, ∑DDT, ∑HCH and ∑CHL were 9.97∼31.7 ng g$\^$-1/, 7.54∼22.6 ng g$\^$-1/, 0.49∼2.0 ng g$\^$-1/, and 0.82∼7.32 ng g$\^$-1/, respectively. Relatively high PCB concentrations in both environmental matrices are found at the inner bay than the outer part, indicating that the sources of PCBs were located inside the bay. DDT compound showed relatively high concentrations in the vicinity of the mouth of river and urban area, whereas other organochlorine pesticides show homogeneous distributions over the bay. Homologue profile of PCB compounds shows that low-chlorinated congeners (especially, di-, tyi- and tetra-) are abundant in Gwangynng Bay, which is diferent from other areas in Korea.

Treatment of hazardous chemicals by Nanoscale Iron powder (나노크기 철 분말을 이용한 난분해성 유해화합물질의 처리)

  • 최승희;장윤영;황경엽;김지형
    • Journal of Korea Soil Environment Society
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    • v.4 no.3
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    • pp.85-93
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    • 1999
  • The destruction of hazardous chemicals such as chlorinated organic compounds(COCs) and nitroaromatic compounds(NACs) by zero-valent iron powder is one of the latest innovative technologies. In this paper. the rapid dechlorination of chlorinated compounds as well as transformation of nitro functional group to amine functional group in the nitroaromatic compounds using synthesized zero-valent iron powder with nanoscale were studied in anaerobic batch system. Nanoscale iron, characterized by high surface area to mass ratios(31.4$\textrm{m}^2$/g) and high reactivity, could quickly reacts with compounds such as TCE, chloroform, nitrobenzene, nitrotoluene, dinitrobenzene and dinitrotoluene, at concentration of 10mg/L in aqueous solution at room temperature and pressure. In this study, the TCE was dechlorinated to ethane and chloroform to methane and nitro groups in NACs were transformed to amino groups in less than 30min. These results indicated that this chemical method using nanoscale iron powder has the high potential for the remediation of soils and groundwater contaminated with hazardous toxic chemicals including chlorinated organic compounds and nitro aromatic compounds.

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Removal of Halogenated Organic Compounds in Wastewater by Pervaporation (투과증발법을 이용한 폐수중의 미량 유기염소계 화합물의 제저)

  • 오부근;하성룡;하상태;이영무
    • Membrane Journal
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    • v.4 no.1
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    • pp.57-62
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    • 1994
  • This study uses pervaporation process to separate small amount of organic trichloroethylene, chloroform and perchloroethylene from contaminated water, since chlorinated hydrocarbones are known to be cancer suspecting compounds. For the separation of small amount of halogenated organic compound dissolved in wastewater, pervaporation membranes should be polymers that possess affinity with orgnic compounds and hydrophobicity. We used polyisobutylene, polyetheramide and polydimethylsiloxane membranes. The degree of affinity between organics and polymers were measured by contact angle method. We had good separation results that separation factor ranged from 34 to 19100 and permeate flux was$19.7~140g/m^2hr$.

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Separation of Aqueous Chlorinated Hydrocarbons by Pervaporation (투과증발법을 이용한 염소계 화합물 수용액의 분리)

  • 이영무;유승민;오부근
    • Membrane Journal
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    • v.6 no.1
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    • pp.53-57
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    • 1996
  • Polysulfone ultrafiltration membrane was coated with polyisobutylene(PIB) as a top layer to separate chlorinated hydrocarbons. The solubility parameter differences between PIB, water and perchloroethylene(PCE) or trichloroethylene(TCE) show that the solubility parameter difference between PIB and TCE or PCE is similar while that between PIB and water is far less, indicating that PIB is selective to chlorinated hydrocarbons. The pervaporation separation of TCE and PCE shows that TCE is concentrated more than four times, by PIB composite membrane, while PCE is concentrated more than thirteen times. This result shows that PIB composite membrane in this study seems to be an appropriate selective layer for the separation of TCE and PCE from aqueous organic solutions.

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Thermal Degradation Characteristics of Carbon Tetrachloride in Excess Hydrogen Atmosphere (과잉수소 반응조건하에서 사염화탄소의 고온 분해반응 특성 연구)

  • Won, Yang-Soo;Jun, Kwan-Soo;Choi, Seong-Pil
    • Journal of Environmental Science International
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    • v.5 no.5
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    • pp.569-577
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    • 1996
  • pure compound chloromethanes; methyl chloride, methylene chloride, chloroform and The carbon tetrachloride were used as a model of chlorocarbon system with Cl/H ratio to investigate thermal stability and hydrodechlorination process of carbon tetrachloride under excess hydrogen atmosphere. The parent thermal stability on basis of temperature required for 99% destruction at 1 second no was evaluated as $875^{\circ}C$ for $CH_3Cl$, $780^{\circ}C$ for $CH_2Cl_2$, $675^{\circ}C$ for $CHCl_3$ and $635^{\circ}C$ for $CCl_4$. Chloroform was thermally less stable than $CCl_4$ at fairly low temperatures $(<570^{\circ}C).$ The lion of $CCl_4$ became more sensitive to increasing temperature, and $CCl_4$ was degraded CHCl3 at above $570^{\circ}C.$ The number and quantity of chlorinated products decreases with increasing temperature for the Product distribution of $CCl_4$ decomposition reaction system. Formation of non-chlorinated hydrocarbons such as $CH_4$, $C_2H_4$ and C_2H_6$ increased as the temperature rise and particularly small amount of methyl chloride was observed above $850^{\circ}C$ in $CC1_4$/$H_2$ reaction system. The less chlorinated products are more stable, with methyl chloride the most stable chlorocarbon in this reaction system.

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