• Title/Summary/Keyword: 수소 열화

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Effect of Electrode Degradation on the Membrane Degradation in PEMFC (PEMFC에서 전극 열화가 전해질 막 열화에 미치는 영향)

  • Song, Jinhoon;Kim, Saehoon;Ahn, Byungki;Ko, Jaijoon;Park, Kwonpil
    • Korean Chemical Engineering Research
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    • v.51 no.1
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    • pp.68-72
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    • 2013
  • Until a recent day, degradation of PEMFC MEA (membrane and electrode assembly) has been studied, separated with membrane degradation and electrode degradation, respectively. But membrane and electrode were degraded coincidentally at real PEMFC operation condition. During simultaneous degradation, there was interaction between membrane degradation and electrode degradation. The effect of electrode degradation on membrane degradation was studied in this work. We compared membrane degradation after electrode degradation and membrane degradation without electrode degradation. I-V performance, hydrogen crossover current, fluoride emission rate (FER), impedance and TEM were measured after and before degradation of MEA. Electrode degradation reduced active area of Pt catalyst, and then radical/$H_2O_2$ evolution rate decreased on Pt. Decrease of radical/$H_2O_2$ reduced the velocity of membrane degradation.

Thermochemical hydrogen production utilization of M-ferrite (M=Co,Ni,Mn) (M-ferrite를 이용한 열화학적 수소제조 (M=Co,Ni,Mn))

  • Cho Mi-Sun;Kim Woo-Jin;Woo Sung-Woong;Park Chu-Sik;Kang Kyoung-Soo;Choi Sang-Il
    • New & Renewable Energy
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    • v.2 no.2 s.6
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    • pp.69-74
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    • 2006
  • 본 연구는 페라이트의 Fe 양이온 일부를 Ni, Mn, Co등으로 치환하여 M-ferrite를 제조하여 열화학적 2단계 물 분해 반응의 특성을 비교 평가하였고, XRD, SEM, GC등의 분석으로 각 금속산화물의 특성을 확인하였다. M-ferrites 는 고상법으로 제조하였다. 각각의 M-ferrite에 대한 열적환원은 1573K 에서 진행하였고 물 분해 반응은 1273K 에서 실시하였다. 이 반응에서 생성된 가스는 전량 포집하여 GC를 통해 분석하였다. 반응 전후의 시료에 대하여 SEM, XRD를 분석하여 GC결과와 함께 금속산화물의 산화환원반응 특성을 고찰하였다. 그 결과로서 물 분해 반응 후 M-ferrite (M=Co, Ni, Mn)의 생성을 XRD를 통하여 확인할 수 있었고, 물 분해 반응과의 비교결과 격자상수의 증대가 M-ferrite내의 산소의 환원에 영향을 미치는 것을 알 수 있었다. SEM결과에서는 4cycle의 물 분해 반응 후 Mn-ferrite의 심한 sintering 현상을 확인 할 수 있었다.

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Thermochemical hydrogen production utilization of M-ferrite (M=Co,Ni,Mn) (M-ferrite를 이용한 열화학적 수소제조(M=Co,Ni,Mn))

  • Cho, Mi-Sun;Kim, Woo-Jin;Woo, Sung-Woong;Park, Chu-Sik;Kang, Kyoung-Soo;Choi, Sang-Il
    • 한국신재생에너지학회:학술대회논문집
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    • 2006.06a
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    • pp.43-46
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    • 2006
  • 본 연구는 페라이트의 Fe 양이온 일부를 Ni, Mn, Co등으로 치환하여 M-ferrites를 제조하여 열화학적 2단계 물 분해 반응의 특성을 비교 평가하였고, XRD, SEM, GC등의 분석으로 각 금속산화물의 특성을 확인하였다. M-ferrites는 고상법으로 제조하였다. 각각의 M-ferrites에 대한 열적환원은 1573K에서 진행하였고 물 분해 반응은 1273K에서 실시하였다. 이 반응에서 생성된 가스는 전량 포집하여 GC를 통해 분석하였다. 반응 전후의 시료에 대하여 SEM, XRD를 분석하여 GC결과와 함께 금속산화물의 산화환원반응 특성을 고찰하였다. 그 결과로서 물 분해 반응 후 M-ferrite (M=Co, Ni, Mn)의 생성을 XRD를 통하여 확인할 수 있었고, 물 분해 반응과의 비교결과 격자상수의 증대가 M-ferrite내의 산소의 환원에 영향을 미치는 것을 알 수 있었다. SEM결과에서는 4cycle의 물 분해 반응 후 Mn-ferrite의 심한 sintering 현상을 확인 할 수 있었다.

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Durability of MEA Using sPEEK Membrane Reinforced with Poly Imide in PEMFC (고분자전해질연료전지에서 폴리이미드 강화 sPEEK막 MEA의 내구성)

  • Lee, Hye-Ri;Na, Il-Chai;Oh, Sung-Jun;Park, Kwon-Pil
    • Korean Chemical Engineering Research
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    • v.55 no.3
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    • pp.296-301
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    • 2017
  • Recently, there are many efforts focused on development of more economical non-fluorinated membranes for PEMFCs (Proton Exchange Membrane Fuel Cells). In this study, sulfonated poly (ether ether ketone) (sPEEK) membrane reinforced with poly imide was made to enhance of membrane durability. In order to test durability of single (un-reinforced) membrane and reinforced membrane MEA (Membrane and Electrode Assembly), degradation accelerated stress test was used. Before and after degradation, I-V polarization curve, hydrogen crossover current, electrochemical surface area, membrane resistance and charge transfer resistance were measured. As a result of experiments, hydrogen crossover current of reinforced MEA was lower than that of single MEA, therefor durability of reinforced MEA was higher than that of single MEA. There was not especially short phenomena in reinforced MEA after degradation accelerated stress test.

High Temperature Thermochemical Treatment and Characterization of Sepiolite for $CO_2$ Storage ($CO_2$ 저장용 Sepiolite의 고온 열화학처리 및 특성평가)

  • Choi, Weon-Kyung;Cho, Tae-Hwan
    • Transactions of the Korean hydrogen and new energy society
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    • v.17 no.4
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    • pp.425-433
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    • 2006
  • Sepiolite was selected as a mineral carbonation candidate ore for carbon dioxide sequestration. Carbonation salt formation from alkaline earth metal ingredient needs to dehydroxylation of sepiolite at high temperature. An evident dehydroxylation was observed over $800^{\circ}C$ and the variations of sepiolite characteristics after high temperature treatment was synthetically evaluated. Remarkable weight loss were measured after high temperature thermochemical reaction then crystallographic and spectroscopic changes were analyzed. The resulted alkaline earth metal oxides could explained by dehydroxylation based on thermochemical reaction.

Bench-scale Test of Sulfuric Acid Decomposition Process in SI Thermochemical Cycle at Ambient Pressure (SI 열화학싸이클 황산분해공정의 Bench-scale 상압 실험)

  • Jeon, Dong-Keun;Lee, Ki-Yong;Kim, Hong-Gon;Kim, Chang-Soo
    • Transactions of the Korean hydrogen and new energy society
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    • v.22 no.2
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    • pp.139-151
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    • 2011
  • The sulfur-iodine (SI) thermochemical water splitting cycle is one of promising hydrogen production methods from water using high-temperature heat generated from a high temperature gas-cooled nuclear reactor (HTGR). The SI cycle consists of three main units, such as Bunsen reaction, HI decomposition, and $H_2SO_4$ decomposition. The feasibility of continuous operation of a series of subunits for $H_2SO_4$ decomposition was investigated with a bench-scale facility working at ambient pressure. It showed stable and reproducible $H_2SO_4$ decomposition by steadily producing $SO_2$ and $O_2$ corresponding to a capacity of 1 mol/h $H_2$ for 24 hrs.

Thermal Behavior of NiFe2O4 for Hydrogen Generation (NiFe2O4를 이용한 열화학 사이클 H2 제조)

  • Han, S.B.;Kang, T.B.;Joo, O.S.;Jung, K.D.
    • Transactions of the Korean hydrogen and new energy society
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    • v.14 no.4
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    • pp.298-304
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    • 2003
  • The thermal behavior of $NiFe_2O_4$ prepared by a solid-state reaction was investigated for $H_2$ generation by the thermochemical cycle. The reduction of $NiFe_2O_4$ started from $800^{\circ}C$, and the weight loss was 0.2-0.3 wt% up to $1000^{\circ}C$. In the $H_2O$ decomposition reaction, $H_2$ was generated by oxidation of reduced $NiFe_2O_4$. The crystal structure of $NiFe_2O_4$ maintained during the redox reaction of 5 cycles. From this observation, the lattice oxygen in $NiFe_2O_4$ is released without the structural change during the thermal reduction and oxygen deficient $NiFe_2O_4$ can be restored to the spinel structure of $NiFe_2O_4$.

Degradation of Thermal Creep by Hydrides of Zr-2/5Nb Pressure Tube (Zr-2.5Nb 압력관의 수소화물에 의한 고온 크리프의 열화거동)

  • Oh, Dong-Joon;Ma, Young-Wha;Yoon, Kee-Bong;Kim, Young-Suk
    • Transactions of the Korean Society of Mechanical Engineers A
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    • v.30 no.12 s.255
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    • pp.1526-1533
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    • 2006
  • The aim of this research was to confirm the existence of the thermal creep degradation by hydrides of Zr-2.5Nb pressure tube materials. Small punch creep tests were performed to obtain the relationship between a creep displacement and a loading period at $300^{\circ}C$. A creep stress and a creep strain rate were also converted from the previous results. The creep material constants and the creep stress exponents at the different hydride contents were compared. Finally the hydrides of the axial and circumferential section were observed using OM, SEM and TEM. The following conclusions were made: 1) The degradation of the thermal creep by hydrides was existed and it strongly depended on the hydride contents. 2) As the hydride contents were increased, the creep stress exponents (m) were also increased. 3) Even though the hydride was not precipitated in 50 ppm materials at $300^{\circ}C$, the degradation of thermal creep was found. Therefore, it was believed that this phenomenon strongly related to the hydride precipitation at room temperature.

Preparation of Carbon Nanomaterials by Thermal CVD and their Hydrogen Storage Properties (열화학기상증착법에 의한 탄소나노소재의 합성 및 수소저장 특성)

  • Yu, Hyung-Kyun;Choi, Won-Kyung;Ryu, Ho-Jin;Lee, Byung-Il
    • Journal of the Korean Ceramic Society
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    • v.38 no.10
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    • pp.867-870
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    • 2001
  • The carbon nanomaterials were prepared using the thermal chemical vapor deposition with ${C_2}{H_2}$ on the Ni-graphite mixture as a supported catalyst. The samples were identified by SEM, TEM, Raman spectroscopy, and the hydrogen storage measurement by electrochemical method was also carried out. The purity of carbon nanotube prepared using ground mixture was higher than that of unground one. Also, the amount of hydrogen storage of purified carbon nanomaterials was more than that of unpurified one.

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