• Journal of Hydrogen and New Energy
• /
• v.28 no.5
• /
• pp.554-560
• /
• 2017

Reduction reactivity of new oxygen carriers for chemical looping combustion system were investigated using $CH_4$ as a reduction gas in a bubbling fluidized bed reactor and compared with that of former SDN70 oxygen carrier. New oxygen carriers showed good reduction reactivity at different $CH_4$ concentration. N018-R2 particle represented better reactivity than SDN70 at high $CH_4$ concentration. N018-R2 particle showed higher fuel conversion and $CO_2$ selectivity than those of SDN70 particle within the temperature range of $750-900^{\circ}C$. Moreover, attrition loss of N018-R2 particle was almost same with that of SDN70 particle. Consequently, we could select N018-R2 particle as the best oxygen carrier.

• Applied Chemistry for Engineering
• /
• v.16 no.3
• /
• pp.328-336
• /
• 2005

In order to remove the NO contained in exhaust gas by the non-selective catalyst reduction method, the catalysts were prepared by varing the loading amount of Ag and V into ${\gamma}-Al_2O_3$. The conversion of $NO_x$ using the prepared catalysts was studied by varying the temperatures, $O_2$ concentrations and $SO_2$ concentrations using. The influence of the catalyst structure on $NO_x$ conversion was studied through the analysis of the physical properties of the prepared catalysts. In the case of $AgV/{\gamma}-Al_2O_3$ catalyst, the $NO_x$ conversion was lower than that of $Ag/{\gamma}-Al_2O_3$ at higher temperatures but higher than that of $Ag/{\gamma}-Al_2O_3$ at lower temperatures. Even though $SO_2$ was contained in the reaction gas, the $NO_x$ conversion did not decrease. Based on the analysis including XRD, XPS, TPR, and UV-Vis DRS before and after the experiments, the experimental results were examined. The results indicated that, $NO_x$ conversion decreased at higher temperatures since Ag oxide could not be maintained well due to the addition of V, whereas it increased at temperatures lower than $300^{\circ}C$ due to the catalytic action of V.

• Journal of the Korean Chemical Society
• /
• v.50 no.4
• /
• pp.315-320
• /
• 2006

manganese oxides have been prepared by Chimie Douce redox reaction between permanganate and chalcogen element fine powder under acidic condition (pH = 1). According to powder X-ray diffraction analyses, the S- and Se-doped manganese oxides are crystallized with layered birnessite and tunnel-type -MnO2 structures, respectively. On the contrary, Te-doped compound was found to be X-ray amorphous. According to EDS analyses, these compounds contain chalcogen dopants with the ratio of chalcogen/manganese = 4-7%. We have investigated the chemical bonding character of these materials with X-ray absorption spectroscopic (XAS) analysis. Mn K-edge XAS results clearly demonstrated that the manganese ions are stabilized in octahedral symmetry with the mixed oxidation states of +3/+4. On the other hand, according to Se K- and Te L1-edge XAS results, selenium and tellurium elements have the high oxidation states of +6, which is surely due to the oxidation of neutral chalcogen element by the strong oxidant permanganate ion. Taking into account their crystal structures and Mn oxidation states, the obtained manganese oxides are expected to be applicable as electrode materials for lithium secondary batteries.

• Clean Technology
• /
• v.29 no.4
• /
• pp.313-320
• /
• 2023

In order to increase the usability of H₂-SCR, the NOx removal characteristics with catalyst powder of PtNi/CeO₂-W-TiO₂ using Ce as a co-catalyst was synthesized and coated on a porous metal structure (PMS) were evaluated. Catalyst powder of PtNi/CeO₂-W-TiO₂(PtNi nanoparticles onto W-TiO₂, with the incorporation of ceria (CeO₂) as a co-catalysts) was synthesized and coated onto a porous metal structure (PMS) to produce a Selective Catalytic Reduction (SCR) catalyst. H₂-SCR with CeO₂ as a co-catalyst exhibited higher NOx removal efficiency compared to H₂-SCR without CeO₂. Particularly, at a 10wt% CeO₂ loading ratio, the NOx removal efficiency was highest at 90℃. As the amount of catalyst coating on PMS increased, the NOx removal efficiency was improved below 90℃, but it was decreased above 120℃. When the space velocity was changed from 4,000 h^-1 to 20,000 h^-1, the NOx removal efficiency improved at temperatures above 120℃. It was expected that the use of the catalyst could be reduced by applying the PMS with excellent specific surface area as a support.

• Proceedings of the Korean Institute of Surface Engineering Conference
• /
• 2013.05a
• /
• pp.174-174
• /
• 2013

현재 자동차 강판 시장에서는 승객들의 안전 확보와 연비 향상을 위하여 자동차 강판의 경량화 및 고장력화가 급속히 진행되고 있다. 더불어 소비자는 더욱 아름답고 멋있는 외관을 추구하면서 정교한 디자인이 가능할 수 있도록 높은 성형성을 갖는 강판에 대한 요구도 또한 증대되고 있다. 따라서 강도와 성형성을 동시에 확보할 수 있는 DP형, TRIP형 등의 다양한 컨셉을 갖는 변태강화형 고장력강에 대한 개발 요구가 점점 심화되고 있으나 이들 고장력강의 상 제어를 위하여 첨가된 Si, Mn등의 성분들이 표면에 안정한 산화물을 형성하기 때문에 이러한 고장력강은 표면 품질이 열위한 것으로 보고 되고 있다. 따라서 기존 연구에서는 열처리중 표면으로 확산되어 올라오는 Si, Mn 산화물의 저감을 위하여 분위기 중 산소농도나 노점등을 조절하거나, 산화전처리, 선도금처리 등을 통하여 Si, Mn 의 표면 선택산화를 제어하여 도금 결함을 최소화하려는 연구가 많이 진행되고 있다. 그러나 이러한 연구들은 대부분 강판 표면에서의 산화/환원의 반응에 대한 분위기 요인을 제어하는 연구들이며 실제 Si, Mn등의 산화성 원소들이 어떠한 조건에서 어떠한 경로들을 통해서 이동하여 표면으로 올라오는지에 대한 연구는 부족한 상황이다. 따라서 본 연구에서는 산화성 원소들의 표면 확산 거동에 대한 고찰을 위하여 다양한 열처리 온도 조건을 통한 표면 도금성 경향, 합급화 경향 및 표면 분석결과를 바탕으로 확산 거동에 대한 경향을 밝히고자 하였다.

• Korean Journal of Materials Research
• /
• v.6 no.10
• /
• pp.1025-1033
• /
• 1996

본 연구에서는 0.5M NaCI 용액내에서 일어나는 고분자재료로 피복된 강의 퇴화현상을 광학현미경 관찰 및 A.C. impedance spectroscopy를 이용하여 연구하였다. 강의 부식은 고분자재료로 피복된 강의 경우 국부부식(localized corrosion)의 형태로 나타난 반면, 피복되지 않은 강의 경우에는 전면부식(uniform corrosion)의 형태로 진행되었다. 고분자재료로 피복된 강의 부식이 국부적으로 진행되는 것은 피복층내에 존재하는 기공이나 크랙과 같은 결함 등에서 부식이 선택적으로 일어나기 때문으로 사료된다. 피복층의 박리(delamination) 현상은 고분자재료로 피복된 강/구리 갈바닉쌍(galvanic couple)의 경우 구리표면 위의 피복층에서만 관찰되었다. 이는 캐소드(cathode)로 작용하는 구리의표면에서 산소의 환원반응에 의해서 형성된 수산화이온(OH-)이 피복층의 박리를 조장하고 있음을 보여준다. 또한, 고분자재료 피복층의 파손 현상은 고분자재료/강의계면에서 석출된 부식생성물에 의해서 크게 조장되고 있음을 알 수 있다.

• Korean Journal of Materials Research
• /
• v.16 no.5
• /
• pp.323-328
• /
• 2006

In situ electrical conductivity measurements on $V_2O_5WO_3/TiO_2$ catalysts were carried out at between 100 and $300^{\circ}C$ under pure oxygen, NO and $NH_3$ to investigate the reaction mechanism for ammonia SCR (selective catalytic reduction) de NOX. The electrical conductivity of catalysts changed irregularly with supply of NO. It was, however, found that the electrical conductivity change with ammonia supply was regular and the increase of electrical conductivity was mainly caused by reduction of the labile surface oxygen. The electrical conductivity change of catalysts showed close relationship with the conversion rate of NOx. Variation of conversion rate in atmosphere without gaseous oxygen also showed that labile lattice oxygen is indispensable in the initial stage of the de NOx reaction. These results suggest that liable lattice oxygen acts decisive role in the de NOx mechanism. They also support that de NOx reaction occurs through the Eley?Rideal type mechanism. The amount of labile oxygen can be estimated from the measurement of electrical conductivity change for catalysts with ammonia supply. This suggests that measurement of the change can be used as a measure of the de NOx performance.

• Proceedings of the Korean Society of Soil and Groundwater Environment Conference
• /
• 2005.04a
• /
• pp.402-404
• /
• 2005

2004년 7월부터 2005년 2월까지 8개월 동안 강원도 정선지역 탄산염지대 지하수 및 하천수의 ${\delta}^{13}C$의 조사 결과, 탄산염 지대 지하수의 13C는 $-12.07{\sim}-8.63$ (평균 -10.34 ), 탄사염지대 하천수의 ${\delta}^{13}C$는 $-10.32{\sim}-6.80$ (평균 -7.944 ) 이었다. 하천수와 지하수 ${\delta}^{13}C$는 수온(T)과 음의 상관관계를 보이고 물의 전기전도도(EC)와 양의 상관관계를 보이며, 여름보다 겨울에 높은 값을 보이는 반면 산화환원 전위(Eh), 용존산소(DO), pH와는 상관관계가 미약함을 보이고 있다. 탄산염지대 지하수 및 하천수의 ${\delta}^{13}C$는 연구지역의 지하수와 하천수가 탄산염암의 용해, 대기 $CO_2$와 용존 $CO_2$의 교환, 유입된 대기 $CO_2$가 물 분자와 반응하여 ${HCO_3}^-$ 이온으로 전환될 때 있는 분별작용의 효과에 의해 주로 영향을 받았으며 수중생물의 신진대사에 의한 변화는 미미한 것으로 나타났다.

• Journal of the Korean Electrochemical Society
• /
• v.17 no.3
• /
• pp.201-208
• /
• 2014

A Pt catalyst ($Pt/G_xC_y$) supported on the hybrid supporting materials composed of graphene oxide (GO) and carbon black (C) was fabricated using polyol method to improve the durability of electrocatalysts. The electrochemical performances measured by cyclic voltammograms using three-electrode system revealed that the properly designed $Pt/G_xC_y$ catalyst exhibited higher durability than that of Pt/C catalyst without sacrificing an electrocatalytic acivity. In the oxygen reduction reaction (ORR) performed in acid solution with the rotating disk electrode, the $Pt/G_xC_y$ catalyst showed greater mass and area-specific activity than those of Pt/C catalyst.

• Journal of Powder Materials
• /
• v.23 no.6
• /
• pp.420-425
• /
• 2016

N-doped carbon nanofibers as catalysts for oxygen-reduction reactions are synthesized using electrospinning and carbonization. Their morphologies, structures, chemical bonding states, and electrochemical performance are characterized. The optimized N-doped carbon nanofibers exhibit graphitization of carbon nanofibers and an increased nitrogen doping as well as a uniform network structure. In particular, the optimized N-doped carbon nanofibers show outstanding catalytic activity for oxygen-reduction reactions, such as a half-wave potential ($E_{1/2}$) of 0.43 V, kinetic limiting current density of $6.2mAcm^{-2}$, electron reduction pathways (n = 3.1), and excellent long-term stability after 2000 cycles, resulting in a lower $E_{1/2}$ potential degradation of 13 mV. The improvement in the electrochemical performance results from the synergistic effect of the graphitization of carbon nanofibers and the increased amount of nitrogen doping.