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마이크로웨이브로 제조된 TS-1 Membrane을 이용한 혼합 자일렌에서의 에틸벤젠 고순도화
전유권,이기천,주영환,최성환,서영종,설용건 한국막학회 2012 멤브레인 Vol.22 No.2
본 연구에서는 혼합 자일렌에서 에틸벤젠을 분리하기 위하여 제올라이트 분리막을 이용하였다. 마이크로웨이브 합성 온도에 변화를 주어 제조한 TS-1 제올라이트 결정을 알루미나 튜브에 성장시키기 위해 3-chloropropyltrimethoxysilane를 코팅 후 TS-1 nano seed를 안착시키고 마이크로웨이브 합성법을 이용한 2차 성장을 통해 3~4 mum의 두께를 가지는 얇은 TS-1 제올라이트 분리막을 제조하였다. 제조한 분리막을 이용하여 에틸벤젠/메타자일렌/파라자일렌이 혼합된 혼합 자일렌으로부터 에틸벤젠을 분리하였다. 마이크로웨이브 합성 온도가 증가할수록 제올라이트 결정의 크기가 비례하여 증가하였다. 또한 반응기의 온도가 200℃에서 가장 높은 투과 플럭스와 선택도를 가졌다. 가장 좋은 에틸벤젠 분리 성능을 보인 분리막은 마이크로웨이브 합성 온도가 170℃인 분리막이고 선택도 값은 2.64였다(에틸벤젠 투과 플럭스 : 1703.0 mol/m2·s·Pa). In this study, separation of ethylbenzene from mixed xylene was performed by using TS-1 zeolite membrane. TS-1 zeolite membranes were prepared by microwave synthesis and changing the reaction temperature. MFI-type TS-1 membranes are synthesized on alumina tubes by functional coating using 3-chloropropyltrimethoxysilane (3CP-TMS). On top surface of interlayer, nano TS-1 crystals were seeded. To form interlayer, microwave-assisted growth of TS-1 zeolite was carried out and thin zeolite layers were produced. All of the prepared membranes are tested to separate ethylbenzene from mixed xylene at different operating temperatures. TS-1 membrane with zeolite seed synthesized at 170℃ compared to 120, 140℃ shows the best ethylbenzene separation at the operation temperature of 200℃ from ternary mixed xylene containing certain composition of ethylbenzene/p-xylene/m-xylene. (separation factor : 2.64, ethylbenzene flux : 1703.0 mol/m2·s·Pa).
전유권,Ohchan Kwon,Yunseong Ji,Ok Sung Jeon,Chanmin Lee,Yong-Gun Shul 한국화학공학회 2019 Korean Chemical Engineering Research(HWAHAK KONGHA Vol.57 No.3
As rechargeable metal-air batteries will be ideal energy storage devices in the future, an active cathode electrocatalyst is required with bi-functionality on both oxygen reduction reaction (ORR) and oxygen evolution reaction (OER) during discharge and charge, respectively. Here, a class of perovskite cathode catalyst with a micro-tubular structure has been developed by controlling bi-functionality from different Ru and Ni dopant ratios. A micro-tubular structure is achieved by the activated carbon fiber (ACF) templating method, which provides uniform size and shape. At the perovskite formula of LaCrO3, the dual dopant system is successfully synthesized with a perfect incorporation into the single perovskite structure. The chemical oxidation states for each Ni and Ru also confirm the partial substitution to Bsite of Cr without any changes in the major perovskite structure. From the electrochemical measurements, the microtubular feature reveals much more efficient catalytic activity on ORR and OER, comparing to the grain catalyst with same perovskite composition. By changing the Ru and Ni ratio, the LaCr0.8Ru0.1Ni0.1O3 micro-tubular catalyst exhibits great bi-functionality, especially on ORR, with low metal loading, which is comparable to the commercial catalyst of Pt and Ir. This advanced catalytic property on the micro-tubular structure and Ru/Ni synergy effect at the perovskite material may provide a new direction for the next-generation cathode catalyst in metal-air battery system.