• 제목/요약/키워드: Zeolite Catalyst

검색결과 160건 처리시간 0.025초

촉매-플라즈마 반응 시스템을 이용한 황화수소의 처리특성 연구 (Characteristics of Hydrogen Sulfide Removal by a Catalyst-assisted Plasma System)

  • 이정근;김혁규;봉춘근;박성진;이명화;황의현;김종호
    • 한국대기환경학회지
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    • 제27권4호
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    • pp.379-386
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    • 2011
  • Catalyst-assisted plasma system with a DBD (Dielectric Barrier Discharge) reactor was used to remove hydrogen sulfide, which is one of the odorous species in this study. The ${\gamma}-Al_2O_3$ and ${\beta}$-Zeolite catalysts impregnated by Ag, Cu and Mn species were employed as catalysts and their $H_2S$ removal characteristics under plasma irradiation were investigated. From the experimental study, we found that the $H_2S$ removal efficiency increases with decreasing space velocity in the system and increasing specific input energy. Furthermore, ${\beta}$-Zeolite catalysts are efficient to remove $H_2S$ than ${\gamma}-Al_2O_3$ catalysts. Especially, the catalysts impregnated by Ag have higher removal efficiency than other catalysts (Cu, Mn).

메조세공 BEA에 고정화된 키랄 Co살렌 착체의 동적분할을 통한 고광학순도의 키랄 모노에스테르 합성 (Synthesis of Optically Active Monoesters via Kinetic Resolution by Chiral Co (Salen) Complex Immobilized on Mesoporous BEA)

  • 최성대;박근우;이경찬;김건중
    • 공업화학
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    • 제26권2호
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    • pp.132-137
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    • 2015
  • BEA형 제올라이트를 알칼리용액으로 처리하여 결정구조 내에 메조세공이 형성되도록 제조하고, 세공 내에 균일계 키랄 Co(III) 살렌을 고정화시켰다. 메조세공 BEA-제올라이트에 고정화된 이핵형 Co-$GaCl_3$ 살렌 촉매는 말단 에폭사이드의 산소고리를 카르복실산으로 여는 키랄 반응에 대하여 높은 활성을 나타내었다. 이 반응을 통하여 라세믹 에폭사이드로부터 다양한 모노 에스테르 유도체를 중간 정도의 광학선택도(47~69 ee%)로 합성할 수 있었다. 키랄(S)-ECH를 반응물로 사용하면, 이들은 키랄 살렌 촉매 존재하에서 카르복시 산에 의하여 에폭사이드의 링이 광학선택적으로 열리며, 생성된 화합물을 염기용액에서 탈염산 처리하면 다시 에폭사이드 링이 형성되면서 광학순도가 매우 높은 모노에스터 에폭사이드 (R)-GB (98 ee% 이상)가 얻어졌다. 고정화촉매는 매우 용이하게 제조될 수 있었으며, 특별한 재생처리 없이 여러번 재사용하여도 촉매의 활성이 유지되었다.

Incorporation of Titanium into H-ZSM-5 Zeolite via Chemical Vapor Deposition: Effect of Steam Treatment

  • Xu, Cheng-Hua;Jin, Tai-Huan;Jhung, Sung-Hwa;Hwang, Jin-Soo;Chang, Jong-San;Qiu, Fa-Li;Park, Sang-Eon
    • Bulletin of the Korean Chemical Society
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    • 제25권5호
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    • pp.681-686
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    • 2004
  • Ti-ZSM-5 prepared by secondary synthesis, from the reaction of H-ZSM-5 with vapor phase $TiCl_4$, was characterized with several physicochemical techniques including FT-IR and UV/VIS-DRS. It was found that zeolite structure, surface area and pore volume did not change, and the framework aluminum could not be replaced by titanium atom during the secondary synthesis of Ti-ZSM-5. The incorporation of titanium into the framework might be due to reaction of $TiCl_4$with the silanol groups associated with defects or surface sites. The formation of extra-framework titanium could not be avoided, unless the samples were further treated by water vapor at 550 $^{\circ}C$ or higher temperature. High temperature steam treatment of Ti-ZSM-5 prepared by chemical vapor deposition with $TiCl_4$was efficient to prevent the formation of non-framework titanium species. Ti-ZSM-5 zeolites prepared in this work contained only framework titanium species and exhibited improved catalytic property close to TS-1 prepared by hydrothermal synthesis.

Photocatalytic removal of NOx using TiO2-coated zeolite

  • Mendoza, Joseph Albert;Lee, Dong Hoon;Kang, Joo-Hyon
    • Environmental Engineering Research
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    • 제21권3호
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    • pp.291-296
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    • 2016
  • Application of photocatalytic nanoparticles has been recently gaining an increased attention as air purifying material for sustainable urban development. The present work reports the photocatalytic removal of gaseous phase nitrogen oxides ($NO_x$) using $TiO_2$-coated zeolite to be applied as a filter media for the urban green infrastructure such as raingardens. The $TiO_2$-coated zeolite was synthesized by simple wet chemistry method and tested in a continuous-flow photo-reactor for its removal efficiency of $NO_x$ under different conditions of the weight percentage of $TiO_2$ coated on the zeolite, and gas retention time. The removal efficiency of $NO_x$ in general increased as the weight percentage of $TiO_2$ coated on the zeolite increased up to 15-20%. Greater than 90% of $NO_x$ was removed at a retention time of one minute using the $TiO_2$-coated zeolite ($TiO_2$ weight percentage = 20%). Overall, $TiO_2$-coated zeolite showed greater efficiency of $NO_x$ removal compared to $TiO_2$ powder probably by providing additional reaction sites from the porous structure of zeolite. It was presumed that the degradation of $NO_x$ is attributed to both the physical adsorption and photocatalytic oxidation that could simultaneously occur at the catalyst surface.

송이로부터 골프장 농약 제거를 위한 합성 제올라이트의 개발 (Development of Synthetic Zeolites from Scoria for Pesticides Removal in the Golf Course)

  • 감상규;안병준;주창식;이민규
    • 한국환경과학회지
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    • 제10권6호
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    • pp.451-459
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    • 2001
  • Adsorption characteristics of triadimefon and diniconazole(pesticide) by natural zeolite($CLI_N$) and several synthetic zeolites were Investigated. The synthetic zeolites used En this study were as follows: Faujasite synthesized from coal fly ash($FAU_F$); Zeolite synthesized from the mixture of FAU and Na-Pl synthesized from the ratio of Cheju scoria 6 to coal fly ash 4 by weight($(FAU + Na-Pl)_{SF}$); waste fluid catalytic cracking catalyst($FCC_W$). The distribution coefficient, $K_D$ and Freundlich constant, $K_F$ decreased in the fellowing sequence : $FCC_W > FAU_F > (FAU + Na-Pl)_{SF} >CLI_N$ among the zeolites. The distribution coefficient and the adsorption capacity of $(FAU + Na-Pl)_{SF}$ for pesticides were 4.4 and 2.6 times higher for triamefon, and 2.0 and 2.4 times higher for diniconazole than those of $CLI_N$, respectively.

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An Efficient Method for N-Formylation of Amines Using Natural HEU Zeolite at Room Temperature Under Solvent-Free Conditions

  • Bahari, Siavash;Mohammadi-Aghdam, Babak;Mohammad Sajadi, S.;Zeidali, Fereshteh
    • Bulletin of the Korean Chemical Society
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    • 제33권7호
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    • pp.2251-2254
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    • 2012
  • A rapid and practical green route for N-formylation of primary and secondary amines with formic acid at room temperature under the solvent-free conditions using HEU zeolite as a heterogeneous, reusable and highly efficient catalyst is described. The process is remarkably simple and environmentally benign. Excellent chemoselectivity was observed for the conversion of primary amines in the presence of secondary amines.

Propylene Aromatization에 미치는 온도 및 촉매의 영향 (Effect of Temperature on Propylene Aromatization over MFI Type Zeolites)

  • 박진우;김상범;곽윤철;신기석;박홍수;함현식
    • 한국응용과학기술학회지
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    • 제19권2호
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    • pp.123-130
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    • 2002
  • [Ga]-MFI and H-ZSM-5 catalysts were synthesized under atmospheric pressure and used in the propylene aromatization. The effect of temperature on the product distribution was also investigated. The catalytic activities of the prepared catalysts were compared with the commercialized H-ZSM-5 which was converted from $NH_{4}$-ZSM-5. In the propylene aromatization, product distribution does not depend on the ratio of Si/$Ga_{2}$ with [Ga]-MFI catalyst, but depend on the ratio of Si/$Al_{2}$ with H-ZSM-5 catalyst [Ga]-MFI catalyst shows better dehydrogenation and alkylation activities than H-ZSM-5 catalyst The addition of Ga to H-ZSM-5 catalyst increases the conversion of propylene, selectivity to aromatics, and alkylation. In the propylene aromatization, the selectivity to aromatics slightly increased with increasing temperature with [Ga]-MFI catalyst, while slightly decreased with increasing temperature with H-ZSM-5 catalyst.

제올라이트 시멘트 모르타르의 재료적 특성에 관한 기초 연구 (A Fundamental study on the Characteristics of Zeolite Cement Mortar)

  • 조병완;강석원;박승국;최지선
    • 콘크리트학회논문집
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    • 제23권2호
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    • pp.203-209
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    • 2011
  • 시멘트 산업은 에너지 다소비형이며 석회석을 원료로 하고 있어 지구 온난화의 주범인 CO를 배출하여, 환경문제로 인해 가까운 시기에 큰 어려움을 겪을 것으로 예상되고 있다. 오늘날 첨단산업의 발전과 지구환경 문제의 심각성에 대한 인식이 증가하여 시멘트 산업에서도 다각화 측면에서 다양한 종류의 기술 등이 활성화되고 있는 시점이다. 이 연구에서는 최근에 새로이 검토되고 있는 시멘트 대체 재료로서 천연 제올라이트를 주원료로 사용한 제올라이트 시멘트 모르타르에 관한 재료적 특성을 분석하는데 목적이 있으며 그 방법으로 물($H_2O$)대신 알칼리 활성제(NaOH)를 사용하여 알칼리 경화반응을 이용한 제올라이트 모르타르를 제조하여, 강도 특성 및 적정 배합비를 구하였다. 그 결과 알칼리 활성제의 양과 경화 온도에 따른 천연 제올라이트 시멘트 모르타르의 7일 압축강도가 42 MPa로 측정되는 등 기존 시멘트보다 뛰어난 성능을 나타내는 것으로 판단되어지며, 기존 건설용 재료를 대체할 가능성이 충분히 있다고 사료된다.

제올라이트 담체상의 디벤조티오펜 수첨탈황반응에서 저온활성 및 선택성 (Activity and Selectivity in Low Temperature for Dibenzothiophene Hydrodesulfurization based Zeolite Support)

  • 김문찬
    • 공업화학
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    • 제9권1호
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    • pp.101-106
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    • 1998
  • 제올라이트를 담체로 사용하여 활성금속으로 코발트와 몰리브덴을 담지시킨 촉매와 상용공정에 사용되는 $NiMo/{\gamma}-Al_2O_3$촉매를 제조하여, 저온에서의 DBT 탈황활성과 선택성에 대하여 비교하였다. 고정층 고압 연속흐름반응기에서 수행된 탈황반응에서, 저온 영역인 $200^{\circ}C$$225^{\circ}C$에서는 제조된 $NiMo/{\gamma}-Al_2O_3$촉매보다 CoMo/zeolite 촉매에서 탈황활성이 더 높았으며, $275^{\circ}C$ 이상의 고온 영역에서는 $NiMo/{\gamma}-Al_2O_3$촉매의 탈황활성이 더 높게 나타났다. $NiMo/{\gamma}-Al_2O_3$촉매에서는 biphenyl과 cyclohexylbenzene이 주생성물인데 비하여 zeolite를 담체로 사용한 촉매의 경우 알킬화반응이 일어나 생성물 분포가 매우 다름을 보여주고 있으며, 알킬화반응과 수소첨가반응의 두 가지 경로를 통해서 최종 생성물질인 alkylcyclohexane을 생성하는 것으로 추정된다. 제올라이트 담체상에서 molybdenum은 flesh 촉매에서 $MoO_3$형태로 존재하고 있으며, aged 촉매상에서는 $MoO_3$$MoS_2$형태로 황화되어 있음을 알 수 있었다.

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제올라이트에 의한 농약의 흡착

  • 감상규;김길성;안병준;이민규
    • 한국지하수토양환경학회:학술대회논문집
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    • 한국지하수토양환경학회 2001년도 총회 및 춘계학술발표회
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    • pp.7-10
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    • 2001
  • Adsorption of the pesticides (phosphamidon, fenitrothion, triadimefon and diniconazole) in natural zeolite (CL $I_{N}$) and several synthetic zeolites was incestigated. The pesticides were not adsorbed on zeolites (Na-Pl, SOD, ANA, JBW and CAN) synthesized from Jeju scoria. The distribution coefficient ( $K_{D}$) and the Freundlich constant ( $K_{F}$) decreased in the following sequences. FC $C_{W}$ (waste catalytic cracking catalyst)>FA $U_{F}$ (FAU Synthesized from coal fly ash)>(FAU+Na-Pl)$_{SF}$ (the mixture of FAU and Na-Pl synthesized from the ratio of Jeju scoria 6 to coal fly ash 4 by weight)>CL $I_{N}$ among the zeolites; diniconazole>fenitrothion> triadimefon>phosphamidon. As the temperature was increased, the amount of pesticide adsorbed per unit mass of zeolite increased for FC $C_{W}$, FA $U_{F}$ and (FAU+Na-Pl)$_{SF}$ but it decreased for CL $I_{N}$, for all the pesticides used in this study. It was independent of pH for phosphamidon, fenitrothion and triadimefon, but decresed as pH was increased for all the zeolites used in this study.y.udy.y.y.y.y.y.y.

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