대한환경공학회지 (Journal of Korean Society of Environmental Engineers)

  • 제28권5호
  • /
  • Pages.511-521
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  • 2006
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  • 1225-5025(pISSN)
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  • 2383-7810(eISSN)
대한환경공학회 (Korean Society of Environmental Engineers)
권호 표지

열공정에서 페놀류로부터 Polychlorinated dibenzo-p-dioxins(PCDDs)과 Polychlorinated dibenzofurans(PCDFs)의 생성에 관한 연구[I]

A Study of Polychlorinated dibenzo-p-dioxins(PCDDs) and Polychlorinated dibenzofurans(PCDFs) Formation from Phenols in Thermal Process[I]

  • 류재용 (대구경북연구원 환경연구팀) ;
  • 서정민 (국립 부산대학교 지역환경시스템) ;
  • 박정호 (국립 진주산업대학교 환경공학과)
  • Ryu, Jae-Yong (Environmental Research Team, Daegu-Gyeongbuk Development Institute) ;
  • Suh, Jeong-Min (Department of Regional Environmental System, Pusan National University) ;
  • Park, Jeong-Ho (Department of Environmental Engineering, Jinju National University)
  • 발행 : 2006.05.31
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초록

페놀류 전구물질로부터 형성된 polychlorinated dibenzo-p-dioxins(PCDDs)와 dibenzofurans(PCDFs)의 모든 동족체와 이성질체의 경향을 페놀과 19개의 염화페놀류의 분포를 이용하여 연구하였다. 실험은 $400^{\circ}C$(particle-mediated formation)와 $600{\sim}700^{\circ}C$(gas-phase formation)에서 각각 행하여 졌으며, 운반가스로 사용된 가스의 조성은 92%의 질소와 8%의 산소를 사용하였다. 염소기가 없는 dibenzo-p-dioxin(DD)와 dibenzofuran(DF)를 포함한 모든 종류의 PCDDs와 PCDFs의 동족체와 이성질체들이 20개의 페놀류를 혼합하여 사용한 본 실험으로부터 얻어졌다. 가스상 실험은 PCDFs가 많이 생성하였고, 입자상 실험에서는 PCDDs를 많이 생성 하였다. 가장 많이 생성된 동족체는 각각 DD와 DF였으며, 염소기의 숫자가 증가할수록, 동족체의 생성량은 감소하였다. 하지만 가스상과 입자상 실험에서 얻어진 PCDDs와 PCDFs의 동족체와 이성질체의 분포는 거의 항상 일정하였다. 고농도로 존재하는 페놀과 적은수의 염소기를 가지고 있는 염화 페놀류의 농도가 가스상과 입자상에서 발생하는 PCDDs와 PCDFs의 분포에 아주 중요한 역활을 하였다.

Homologue and isomer patterns of polychlorinated dibenzo-p-dioxins(PCDDs) and polychlorinated dibenzofurans(PCDFs) congeners formed from phenols in the gas-phase at $600{\sim}700^{\circ}C$ and via particle-mediated reactions at $400^{\circ}C$ were studied in an isothermal flow reactor. A mixture of 20 phenols in relative concentrations found in a municipal waste incinerator(MWI) stack gas was used for this study. PCDDs and PCDFs homologue and isomer patterns obtained from the phenol. From the phenol experiments, gas-phase formation at $600{\sim}700^{\circ}C$ favors PCDFs formation whereas particle-mediated formation at $400^{\circ}C$ favors PCDDs formation. DD and DF were most abundant homologue groups, PCDDs and PCDFs homologue fraction decreased with increasing number of chlorine substituents. PCDDs and PCDFs homologue and isomer fractions were almost constant from gas-phase formation and particle-mediated formation. Unsubstituted phenol, which was present in high concentration, played a significant role in the formation of PCDD/Fs congeners under both sets of experimental conditions.

키워드

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