• 전기학회논문지
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• 제59권5호
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• pp.932-938
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• 2010

This paper proposed the effective treatment method for organic substances using the barrier discharge plasma process and catalytic chemical reaction followed from ozone decomposition. The decomposition by the plasma process of organic substances such as trichloroethylene, methyl alcohol, acetone, and dichloromethane carried out, and ozone is generated effectively at the same time. By passing through catalysts, ozone easily decomposed and further decomposed organic substances. And, 2-dimensional distribution of ozone using the optical measurement method is performed to identify the catalytic surface chemical reaction. In addition, CO is easily oxidized into $CO_2$ by this chemical reaction, which might be induced oxygen atom radicals formed at the surface of catalyst from ozone decomposition.

• 한국전기전자재료학회:학술대회논문집
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• 한국전기전자재료학회 2005년도 하계학술대회 논문집 Vol.6
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• pp.552-553
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• 2005

In order to improve energy efficiency in the dilute trichloroethylene removal using the nonthermal plasma process, the barrier discharge treatment combined with manganese dioxide was experimentally studied. Reaction kinetics in this process was studied on the basis of final byproducts distribution. Decomposition efficiency was improved to about 99% at the specific energy 40J/L with passing through manganese dioxide. C=C $\pi$ bond cleavage in TCE gave DCAC (single bond, C-C) through oxidation reaction during the barrier discharge plasma treatment. Those DCAC were broken easily in the subsequent catalytic reaction due to the weak bonding energy about 3 ~ 4 eV compared with the double bonding energy in TCE molecules. Oxidation byproducts of DCAC and TCAA from TCE decomposition are generated from the barrier discharge plasma treatment and catalytic surface chemical reaction, respectively. Complete oxidation of TCE into $CO_X$ is required to about 400J/L.

• 한국진공학회:학술대회논문집
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• 한국진공학회 2013년도 제45회 하계 정기학술대회 초록집
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• pp.140.2-140.2
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• 2013

Strong metal-support interaction effect is an important issue in determining the catalytic activity for heterogeneous catalysis. In this work, we report the catalytic activity of $Au/TiO_2$, $Au/Al_2O_3$, and $Au/Al_2O_3-CeO_2$ nanocatalysts under CO oxidation fabricated by arc plasma deposition (APD), which is a facile dry process with no organic materials involved. These catalytic materials were characterized by transmission electron microscopy (TEM), energy-dispersive X-ray spectroscopy (EDS) and $N_2$-physisorption. Catalytic activity of the materials has measured by CO oxidation using oxygen, as a model reaction, in a micro-flow reactor at atmospheric pressure. Using APD, the catalyst nanoparticles were well dispersed on metal oxide powder with an average particle size (3~10 nm). As for catalytic reactivity, the result shows $Au/Al_2O_3-CeO_2$ nanocatalyst has the highest catalytic activity among three samples in CO oxidation, and $Au/TiO_2$, and $Au/Al_2O_3$ in sequence. We discuss the effects of structure and metal-oxide interactions of the catalysts on catalytic activity.

• 한국진공학회:학술대회논문집
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• 한국진공학회 2013년도 제44회 동계 정기학술대회 초록집
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• pp.261-261
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• 2013

The smart design of nanocatalysts can improve the catalytic activity of transition metals on reducible oxide supports, such as titania, via strong metal-support interactions. In this work, we investigatedtwo-dimensional Pt nanoparticle/titania catalytic systems under the CO oxidation reaction. Arc plasma deposition (APD) and metal impregnation techniques were employed to achieve Pt nanoparticle deposition on titania supports, which were prepared by multitarget sputtering and sol-gel techniques. APD Pt nanoparticles with an average size of 2.7 nm were deposited on sputtered and sol-gel-prepared titania films to assess the role of the titania support on the catalytic activity of Pt under CO oxidation. In order to study the nature of the dispersed metallic phase and its effect on the activity of the catalytic CO oxidation reaction, Pt nanoparticles were deposited in varying surface coverages on sputtered titania films using arc plasma deposition. Our results show an enhanced activity of Pt nanoparticles when the nanoparticle/titania interfaces are exposed. APD Pt shows superior catalytic activity under CO oxidation, as compared to impregnated Pt nanoparticles, due to the catalytically active nature of the mild surface oxidation and the active Pt metal, suggesting that APD can be used for large-scale synthesis of active metal nanocatalysts.

• 공업화학
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• 제17권4호
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• pp.414-419
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• 2006

연소 배기가스 중의 수분, 탄화수소 및 CO가 저온 플라즈마 및 $NH_{3}$ SCR (Selective Catalytic Reduction)공정이 복합된 탈질공정에 미치는 영향에 대한 연구가 수행되었다. 실험결과 일반적인 SCR 반응에 비해 매우 빠른 반응속도를 갖는 fast SCR 반응은 $150{\sim}200^{\circ}C$의 저온조건에서 탈질율의 상승을 가져다주지만, 처리가스 중에 탄화수소가 있는 경우 fast SCR 반응의 역할이 상당히 감소되는 것을 확인할 수 있었다. 이는 저온 플라즈마 반응기에서 부분산화반응을 통해 탄화수소 중 일부가 알데히드로 전환되며, 알데히드는 fast SCR 반응에 있어 중요한 변수인 $NO_{2}/NO_{x}$ 비율에 영향을 주기 때문인 것으로 설명되었다. 한편, 수분 및 CO가 fast SCR 반응에 미치는 영향은 탄화수소에 비해 상대적으로 적음을 확인할 수 있었다.

• 한국전기전자재료학회논문지
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• 제19권3호
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• pp.292-300
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• 2006

In order to improve energy efficiency in the dilute trichloroethylene removal using the nonthermal plasma process, the barrier discharge treatment combined with manganese dioxide was experimentally studied. Reaction kinetics in this process was studied on the basis of final byproducts distribution. Decomposition efficiency was improved to about $99\;\%$ at the specific energy of 40 J/L with passing through manganese dioxide. C=C ${\pi}$ bond cleavage of TCE substances gave DCAC, which has the single bond of C-C through oxidation reaction during the barrier discharge plasma treatment. Those DCAC were broken easily in the subsequent catalytic reaction due to the weak bonding energy about $3{\sim}4\;eV$ compared with the double bonding energy in TCE molecules. Oxidation byproducts of DCAC and TCAA from TCE decomposition are generated from the barrier discharge plasma treatment and catalytic surface chemical reaction, respectively. Complete oxidation of TCE into COx is required to about 400 J/L, but $CO_2$ selectivity remains about $60\;\%$.

• 한국표면공학회지
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• 제51권3호
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• pp.179-184
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• 2018

In this study, Ni and tungsten carbide (WC) nanoparticles are simultaneously synthesized with the mesoporous carbon nanoparticles (CNP) using a solution plasma processing (SPP) in the benzene. The Ni and WC nanoparticles were formed through the sputtering effect of electrodes during discharge, and mean time CNP were formed through reduction reaction. TEM observation showed that loaded Ni and WC nanoparticles were evenly dispersed on the CNP. The results of electrochemical analysis demonstrated that an introduction of Ni nanoparticles promoted to improve catalytic activity for oxygen reduction reaction (ORR). Moreover, Ni-WC/CNP lead to fast electron transfer process compared to that of WC/CNP. Therefore, the inexpensive Ni-WC/CNP might be a promising as catalytic material for cathodes in fuel cell applications.

• 한국가스학회지
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• 제5권1호
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• pp.15-20
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• 2001

저온 마이크로웨이브 플라즈마와 촉매반응에 의한 메탄올 활성화하여 C2+ 화합물과 수소로 전환하는 반응을 고찰하였다. 금속 촉매인 Fe, Ni과 귀금속 촉매인 Pt, Pd 계열의 촉매로 본 실험을 수행하였다 메탄의 유속이 $20ml\;min^{-1}$일때 플라즈마의 출력이 증가할수록 C2+ 생성물은 29에서 $42\%$로 증가하였으며 동시에 메탄의 커플링 반응에서 발생하는 수소는 0.6에서 0.65 몰분율을 나타내었다. 촉매는 플라즈마 영역 후단에 위치하였을 때, C2+ 생성물이 일정한 수율을 나타내는 반면 에틸렌과 아세틸렌의 선택도는 향상되었다. 플라즈마 반응후 ECR 전기장과 Pd-Ni 이원촉매를 위치했을 때 최고의 C2+ 수율은 $64\%$로 관찰되었다.

• 공업화학
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• 제25권5호
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• pp.497-502
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• 2014

상압 플라즈마 반응기 내에 Ni-$Al_2O_3$와 Ni-$MgAl_2O_4$ 촉매를 충진한 하이브리드 반응기를 이용하여 메탄과 이산화탄소의 전환반응을 진행하였다. 인가전력, 반응가스 유량, 혼합비율 및 반응기 온도 등 다양한 공정변수와 촉매의 충진 유무에 따른 메탄과 이산화탄소의 전환반응 특성이 분석되었다. 촉매의 반응 기여도 분석에서 공정온도를 $400^{\circ}C$까지 올린 경우에도 플라즈마 방전이 없이는 메탄과 이산화탄소의 촉매를 통한 자발적 전환반응이 일어나지 않았다. 이는 촉매를 충진하지 않은 플라즈마 방전만의 전환공정과의 비교를 통하여 확인할 수 있었다. 플라즈마 반응기에 촉매를 적용하는 경우에는 공정의 적절성과 전환처리에 적합한 촉매의 선택이 필수적이다.

• Bulletin of the Korean Chemical Society
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• 제35권10호
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• pp.3035-3040
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• 2014

A new efficient catalytic method for aza/thia-Michael addition reactions of amines/thiols with higher product yields has been developed. Combining single-walled carbon nanotubes (SWCNT) with triethylammonium hydrogen phosphate (TEAP) ionic liquid (IL) can work as a catalyst. We utilized Raman spectroscopy to gain insight into the interactions between IL and SWCNT. The interactions between SWCNT with TEAP were confirmed by the increasing intensity ratios and spectral shift in wavelength of the Raman D and G bands of SWCNT. Further, the morphology of the resulting composite materials of TEAP and SWCNT was determined by using scanning electron microscopy (SEM). Higher product yield in reduced reaction time is the key advantage of using bucky gel as a catalyst for Michael reaction.