• 제목/요약/키워드: OER

검색결과 87건 처리시간 0.027초

산소부화연소에서 Co2 첨가에 대한 연소 특성 (Characteristics for Effects of Co2 Addition to Oxygen-Enriched Combustion)

  • 김한석;김호근;안국영;김용모
    • 대한기계학회논문집B
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    • 제28권1호
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    • pp.9-15
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    • 2004
  • $CO_2$ is a well-known green house gas as well as the major source of global warming. Many researchers have studied to reduce $CO_2$ emission in combustion processes. Among the method for reducing $CO_2$ emission, oxygen-enriched combustion has been proposed. Because its adiabatic flame temperature is relatively too high, existing facilities must be changed or the flame temperature in the combustion zone should be reduced. The combustion characteristics, composition in the flame zone, temperature profile and emission gases were investigated experimentally for the various oxygen-enriched ratios(OER) by the addition of $CO_2$, under constant $O_2$ flow rate. Results showed that the reaction zone was quenched and broadened as the addition of $CO_2$ was increased. The emission of NOx in flue gas was decreased as decreasing temperature in reaction zone. It was also shown that the reaction was delayed by the cooling effect. As the addition of $CO_2$ was increased, the composition of CO in the flame zone was increased due to the increase of reaction rate by increasing mixing effect of oxidant/fuel at OER=0%, but the composition of CO was decreased by quenching effect at OER=50% and 100%.

산소부화연소에서 $CO_2$ 첨가에 대한 영향 (Effects of $CO_2$ addition to Oxygen-Enriched Combustion)

  • 김호근;김한석;안국영;김용모
    • 대한기계학회:학술대회논문집
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    • 대한기계학회 2003년도 춘계학술대회
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    • pp.1389-1394
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    • 2003
  • $CO_2$ is a well-known green house gas, which is the major source of global warming. Many researchers have studied to reduce $CO_2$ emission in combustion processes. Among the method for reducing $CO_2$ emission, oxygen-enriched combustion has been proposed. But the adiabatic flame temperature is too high. So existing facilities must be changed, or the adiabatic flame temperature in the combustion zone should be reduced. The combustion characteristics, composition in the flame zone, temperature profile and emission gases were studied experimentally for the various oxygen-enriched mtios(OER) by addition of $CO_2$ under coustant $O_2$ flowrate. Results showed that the reaction zone was quenched, broadened, as addition of $CO_2$ was increased. Temperature has a large effect on the NOx emission. The emission of NOx in flue gas decreased due to the decreased temperature of reaction zone. It was also shown that the reaction was delayed by the cooling effect. As the addition of $CO_2$ was increased, the composition of CO in the flame zone increased due to the increase of reaction rate by increasing mixing effect of oxidant/fuel at OER=0, but the composition of CO decreased by quenching effect at OER=50 and 100%.

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Rational Design of Binder-Free Fe-Doped CuCo(OH)2 Nanosheets for High-Performance Water Oxidation

  • Patil, Komal;Jang, Su Young;Kim, Jin Hyeok
    • 한국재료학회지
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    • 제32권5호
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    • pp.237-242
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    • 2022
  • Designing and producing a low-cost, high-current-density electrode with good electrocatalytic activity for the oxygen evolution reaction (OER) is still a major challenge for the industrial hydrogen energy economy. In this study, nanostructured Fe-doped CuCo(OH)2 was discovered to be a precedent electrocatalyst for OER with low overpotential, low Tafel slope, good durability, and high electrochemically active surface sites at reduced mass loadings. Fe-doped CuCo(OH)2 nanosheets are made using a hydrothermal synthesis process. These nanosheets are clumped together to form a highly open hierarchical structure. When used as an electrocatalyst, the Fe-doped CuCo(OH)2 nanosheets required an overpotential of 260 mV to reach a current density of 50 mA cm-2. Also, it showed a small Tafel slope of 72.9 mV dec-1, and superior stability while catalyzing the generation of O2 continuously for 20 hours. The Fe-doped CuCo(OH)2 was found to have a large number of active sites which provide hierarchical and stable transfer routes for both electrolyte ions and electrons, resulting in exceptional OER performance.

Fe-doped β-Ni(OH)2의 산소발생반응 증가를 위한 Mo의 동시도핑효과 (Effects of Mo co-doping into Fe doped β-Ni(OH)2 microcrystals for oxygen evolution reactions)

  • 박제홍;유시범;안태광;김병준;유정호
    • 한국결정성장학회지
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    • 제34권1호
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    • pp.30-35
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    • 2024
  • 수소에너지 생산을 위한 물분해 시스템의 효율을 향상시키기 위해서는, 수소발생반응(HER)과 산소발생반응(OER) 각각에서 촉매로 인한 전기화학적 반응에서의 높은 과전압의 감소가 수반되어야 한다. 그 중에서도 전이금속 기반의 화합물들은 현재 상용되고 있는 백금 등의 귀금속을 대체할 촉매 재료로써 주목받고 있다. 본 연구에서는, 저렴한 금속 다공성 소재인 니켈폼(Ni foam)을 지지체로 사용하고, 수열합성 공정을 통해 Fe-doped β-Ni(OH)2 마이크로결정을 합성하였다. 또한 OER 특성을 향상시키기 위하여 Mo을 동시도핑하여 합성된 Fe-Mo co-doped β-Ni(OH)2 마이크로결정의 형상, 결정구조 및 수전해 특성의 변화를 관찰하였으며, 상용 수전해 시스템의 촉매로서의 적용가능성을 검토하였다.

전기화학적 방법을 이용한 산소 발생용 Blue TiO2 전극제조 및 반응특성조사 (Electrochemical preparation of Blue TiO2 nanotube array and its application for oxygen evolution reaction)

  • 한준혁;탁용석;윤제용
    • 한국표면공학회:학술대회논문집
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    • 한국표면공학회 2014년도 추계학술대회 논문집
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    • pp.46-46
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    • 2014
  • 알칼리 수전해는 신재생에너지를 이용하여 오염물질 없이 효율적으로 수소를 생산할 수 있는 방법 중의 하나이다. 알칼리 수전해 시스템의 산화전극으로 불용성전극이 많이 사용되고 있으나 높은 과전압과 제조 공정이 복잡한 문제점을 가지고 있다. 본 연구에서는 전기변색을 이용해 짙은 파란색의 $TiO_2$ 나노튜브를 알칼리 수전해 시스템의 산화전극으로 이용하고자 하였다. 양극산화법을 이용해 $TiO_2$ 나노튜브를 만드는 과정에서 양극산화 시간과 인가전압에 따라 Blue $TiO_2$의 산소발생반응(Oxygen evolution reaction, OER) 활성 변화를 측정하였고 나노튜브 길이가 길고 직경이 클수록 OER활성과 내구성이 향상되는 것을 확인하였다.

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교육정보 자유이용체제 구축을 위한 서비스 모델에 관한 연구 (A Study on Service Models for the Building of Open Educational Resource Service System)

  • 박정호;강장묵
    • 한국인터넷방송통신학회논문지
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    • 제11권2호
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    • pp.73-81
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    • 2011
  • 이 글은 교사나 연구사들이 저작권 침해 걱정 없이 교육용 콘텐츠를 다운로드받아 자유롭게 이용하거나 자신이 직접 만든 교육용 콘텐츠를 업로드 하여 타인과 공유할 수 있도록 하기 위한 '교육정보자유이용체제'의 구축 방안에 관한 연구이다. 본 논문에서는 우선적으로 '교육정보자유이용체제'와 유사한 성격을 가진 국내외 공개교육자원(OER, Open Educational Resource) 서비스들의 구축 형태를 분석한다. 그리고 이러한 분석 결과를 바탕으로 '교육정보자유이용체제'를 단계적으로 확장하여 구축하기에 적합한 새로운 모델들을 제시한다. 본 논문에서 제시한 모델들은 '수요자 중심형 모델', '사용자 참여형 모델', '집중 관리형 모델', '콘텐츠 신디케이션형 모델'에 해당하는 네 가지 모델로써 단계적으로 확장하여 구축하는 것이 가능하기 때문에 이용자의 요구사항을 유연성 있게 수용할 수 있다. 특히 기존 '전국교육정보공유체제'가 가졌던 저작권 관련 문제점을 단계적으로 해결할 수 있는 장점을 가진다.

A Review on Membranes and Catalysts for Anion Exchange Membrane Water Electrolysis Single Cells

  • Cho, Min Kyung;Lim, Ahyoun;Lee, So Young;Kim, Hyoung-Juhn;Yoo, Sung Jong;Sung, Yung-Eun;Park, Hyun S.;Jang, Jong Hyun
    • Journal of Electrochemical Science and Technology
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    • 제8권3호
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    • pp.183-196
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    • 2017
  • The research efforts directed at advancing water electrolysis technology continue to intensify together with the increasing interest in hydrogen as an alternative source of energy to fossil fuels. Among the various water electrolysis systems reported to date, systems employing a solid polymer electrolyte membrane are known to display both improved safety and efficiency as a result of enhanced separation of products: hydrogen and oxygen. Conducting water electrolysis in an alkaline medium lowers the system cost by allowing non-platinum group metals to be used as catalysts for the complex multi-electron transfer reactions involved in water electrolysis, namely the hydrogen and oxygen evolution reactions (HER and OER, respectively). We briefly review the anion exchange membranes (AEMs) and electrocatalysts developed and applied thus far in alkaline AEM water electrolysis (AEMWE) devices. Testing the developed components in AEMWE cells is a key step in maximizing the device performance since cell performance depends strongly on the structure of the electrodes containing the HER and OER catalysts and the polymer membrane under specific cell operating conditions. In this review, we discuss the properties of reported AEMs that have been used to fabricate membrane-electrode assemblies for AEMWE cells, including membranes based on polysulfone, poly(2,6-dimethyl-p-phylene) oxide, polybenzimidazole, and inorganic composite materials. The activities and stabilities of tertiary metal oxides, metal carbon composites, and ultra-low Pt-loading electrodes toward OER and HER in AEMWE cells are also described.

산소발생반응을 위한 CuCo2O4 나노섬유 전기화학 촉매 합성 및 특성 분석 (Synthesis and Characterization of CuCo2O4 Nanofiber Electrocatalyst for Oxygen Evolution Reaction)

  • 원미소;장명제;이규환;김양도;최승목
    • 한국표면공학회지
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    • 제49권6호
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    • pp.539-548
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    • 2016
  • The non-noble 1D nanofibers(NFs) prepared by electrospinning and calcination method were used as oxygen evolution reaction (OER) electrocatalyst for water electrolysis. The electrospinning process and rate of solution composition was optimized to prepare uniform and non-beaded PVP polymer electrospun NFs. The diameter and morphology of PVP NFs changed in accordance with the viscosity and ion conductivity. The clean metal precursor contained electrospun fibers were synthesized via the optimized electrospinning process and solution composition. The calcined $CuCo_2O_4$ NFs catalyst showed higher activity and long-term cycle stability for OER compared with other $Co_3O_4$, $NiCo_2O$ NF catalysts. Furthermore, the $CuCo_2O_4$ NFs maintained the OER activity during long-term cycle test compared with commercial $CuCo_2O_4$ nanoparticle catalyst due to unique physicochemical and electrochemical properties by1D nanostructure.

알칼리용액에서 산소환원 및 발생반응에 대한 La0.8Sr0.2CoO3 전극의 기체확산층 영향 (Effect of Gas Diffusion Layer on La0.8Sr0.2CoO3 Bifunctional Electrode for Oxygen Reduction and Evolution Reactions in an Alkaline Solution)

  • 로페즈 카린;양진현;선호정;박경세;엄승욱;임형렬;이홍기;심중표
    • 한국수소및신에너지학회논문집
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    • 제27권6호
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    • pp.677-684
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    • 2016
  • Various commercially available gas diffusion layers (GDLs) from different manufacturers were used to prepare an air electrode using $La_{0.8}Sr_{0.2}CoO_3$ perovskite (LSCP) as the catalyst for the oxygen reduction reaction (ORR) and oxygen evolution reaction (OER) in an alkaline solution. Various GDLs have different physical properties, such as porosity, conductivity, hydrophobicity, etc. The ORR and OER of the resulting cathode were electrochemically evaluated in an alkaline solution. The electrochemical properties of the resulting cathodes were slightly different when compared to the physical properties of GDLs. Pore structure and conductivity of GDLs had a prominent effect and their hydrophobicities had a minor effect on the electrochemical performances of cathodes for ORR and OER.