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Degradation of Volatile Hydrocarbons Using Continuous-Flow Photocatalytic Systems with Enhanced Catalytic Surface Areas
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  • Degradation of Volatile Hydrocarbons Using Continuous-Flow Photocatalytic Systems with Enhanced Catalytic Surface Areas
  • Degradation of Volatile Hydrocarbons Using Continuous-Flow Photocatalytic Systems with Enhanced Catalytic Surface Areas
저자명
Jo. Wan-Kuen,Yang. Sung-Hoon,Shin. Seung-Ho,Yang. Sung-Bong
간행물명
Environmental engineering research
권/호정보
2011년|16권 2호|pp.91-96 (6 pages)
발행정보
대한환경공학회
파일정보
정기간행물|ENG|
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이 논문은 한국과학기술정보연구원과 논문 연계를 통해 무료로 제공되는 원문입니다.
서지반출

기타언어초록

Limited information is available on the degradation of volatile hydrocarbons determined via the use of plate-inserted photocatalytic reactors. This has led to the evaluation of surface areas of cylindrical continuous-flow photocatalytic reactors for the degradation of three selected aromatic hydrocarbons. Three types of reactors were prepared: a double cylinder-type, a single cylindrical-type without plates and a single cylindrical-type with inserted glass tubes. According to diffuse reflectance, FTIR and X-ray diffraction (XRD) spectroscopy, the surface characteristics of a coated photocatalyst were very similar to those of raw $TiO_2$, thereby suggesting that the coated photocatalyst exhibited the same photocatalytic activity as the raw $TiO_2$. The photocatalytic degradation efficiencies were significantly or slightly higher for the single cylinder-type reactor than for the double cylinder-type reactor which had a greater catalytic surface area. However, for all target compounds, the degradation efficiencies increased gradually when the number of plates was increased. Accordingly, it was suggested that the surface area being enhanced for the plate-inserted reactor would elevate the photocatalytic degradation efficiency effectively. In addition, this study confirmed that both initial concentrations of target compounds and flow rates were important parameters for the photocatalytic removal mechanism of these plate-inserted photocatalytic reactors.