• Title/Summary/Keyword: Catalyst durability

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The Effect of Pt and La Promoted on Cobalt-Based Catalyst for CO2 Dry Reforming (이산화탄소 건식 개질반응을 위한 코발트계 촉매에서 Pt와 La의 영향)

  • Lee, Hye-Hyun;Song, Sang-Hoon;Chang, Tae-Sun;Hong, Ji-Sook;Suh, Jeong-Kwon;Lee, Chang-Yong
    • Applied Chemistry for Engineering
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    • v.22 no.2
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    • pp.161-166
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    • 2011
  • The $CO_2$ dry reforming reaction, which converts carbon dioxide to hydrogen and carbon monoxide, is typical endothermic reaction, and also known as adverse reaction owing to thermodynamics. In order to overcome the problem, the development studies of suitable catalyst based on precious metals for high durability of thermal and optimization of life time have been examined but it had economical problem by high cost. In this study, we confirmed optimum contents of Pt and La with such different contents of Pt (0.02~0.2 wt%) or La (2~20 wt%) over $Co/SiO_2$ which prepared for excellent activity and cost-effective catalysts. As a result, the promoted catalysts with 0.04 wt% Pt or 9 wt% La over $Co/SiO_2$ showed the highest activity which is 57% and 55% $CO_2$ conversion respectively. Also, the particle size of cobalt on the promoted catalysts with 0.04 wt% Pt or 9 wt% La by characterization of catalyst could confirm the smallest particle size in this study. Therefore, it could know that particle size of cobalt had effected the stability and reactivity of catalysts due to the contents of Pt and La.

Effect of Evaluation Conditions on Electrochemical Accelerated Degradation of PEMFC Polymer Membrane (PEMFC 고분자 막의 전기화학적 가속 열화에 미치는 평가조건들의 영향)

  • Sohyeong Oh;Donggeun Yoo;Suk Joo Bae;Sun Geu Chae;Kwonpil Park
    • Korean Chemical Engineering Research
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    • v.61 no.3
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    • pp.356-361
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    • 2023
  • In order to improve the durability of the proton exchange membrane fuel cell (PEMFC), it is important to accurately evaluate the durability of the polymer membrane in a short time. The test conditions for chemically accelerated durability evaluation of membranes are high voltage, high temperature, low humidity, and high gas pressure. It can be said that the protocol is developed by changing these conditions. However, the relative influence of each test condition on the degradation of the membrane has not been studied. In chemical accelerated degradation experiment of the membrane, the influence of 4 factors (conditions) was examined through the factor experiment method. The degree of degradation of the membrane after accelerated degradation was determined by measuring the hydrogen permeability and effluent fluoride ion concentration, and it was possible to determine the degradation order of the polymer membrane under 8 conditions by the difference in fluoride ion concentration. It was shown that the influence of the membrane degradation factor was in the order of voltage > temperature > oxygen pressure > humidity. It was confirmed that the degradation of the electrode catalyst had an effect on the chemical degradation of the membrane.

Effect of Graphitized Carbon Supports on Electrochemical Carbon Corrosion in Polymer Electrolyte Membrane Fuel Cells (탄소 담지체의 결정성에 따른 고분자전해질형 연료전지의 내구성 평가 연구)

  • Oh, Hyung-Suk;Sharma, Raj Kishore;Haam, Seung-Joo;Lee, Chang-Ha;Kim, Han-Sung
    • Journal of the Korean Electrochemical Society
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    • v.12 no.2
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    • pp.142-147
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    • 2009
  • The influence of graphitization of carbon support on the electrochemical corrosion of carbon and sintering of Pt particles are investigated by measuring $CO_2$ emission at a constant potential of 1.4 V for 30 min using on-line mass spectrometry and cyclic voltammogram. In comparison to commercial Pt/C (from Johnson Matthey), highly graphitized carbon nanofiber (CNF) supported Pt catalyst exhibits lower performance degradation and $CO_2$ emission. As the more carbon corrosion occurred, the more prominent changes were detected in electrochemical characteristics of fuel cell. This indicates that the carbon corrosion affects significantly the fuel cell durability. From the observed results, CNF is considered to be more corrosion resistant material as a catalyst support. However, CNF shows higher aggregation of Pt particles under repeated cyclic voltammetry between 0 and 0.8 V where the carbon corrosion is not initiated.

Effects of Hardeners and Catalysts on the Reliability of Copper to Copper Adhesive Joint (Cu-Cu 접착부의 고온고습 내구성에 미치는 경화제 및 촉매제의 영향)

  • Min, Kyung-Eun;Kim, Hae-Yeon;Bang, Jung-Hwan;Kim, Jong-Hoon;Kim, Jun-Ki
    • Korean Journal of Materials Research
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    • v.21 no.5
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    • pp.283-287
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    • 2011
  • As the performance of microelectronic devices is improved, the use of copper as a heat dissipation member is increasing due to its good thermal conductivity. The high thermal conductivity of copper, however, leads to difficulties in the joining process. Satisfactory bonding with copper is known to be difficult, especially if high shear and peel strengths are desired. The primary reason is that a copper oxide layer develops rapidly and is weakly attached to the base metal under typical conditions. Thus, when a clean copper substrate is bonded, the initial strength of the joint is high, but upon environmental exposure, an oxide layer may develop, which will reduce the durability of the joint. In this study, an epoxy adhesive formulation was investigated to improve the strength and reliability of a copper to copper joint. Epoxy hardeners such as anhydride, dihydrazide, and dicyandiamide and catalysts such as triphenylphosphine and imidazole were added to an epoxy resin mixture of DGEBA and DGEBF. Differential scanning calorimetry (DSC) analyses revealed that the curing temperatures were dependent on the type of hardener rather than on the catalyst, and higher heat of curing resulted in a higher Tg. The reliability of the copper joint against a high temperature and high humidity environment was found to be the lowest in the case of dihydrazide addition. This is attributed to its high water permeability, which led to the formation of a weak boundary layer of copper oxide. It was also found that dicyandiamide provided the highest initial joint strength and reliability while anhydride yielded intermediate performance between dicyandiamide and dihydrazide.

A Study on Optimization of Catalyst Injection Controller for Reducing Soot (Soot 저감을 위한 촉매 분사 최적화 방안 연구)

  • Kim Byeong-Woo
    • Journal of the Korea Academia-Industrial cooperation Society
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    • v.7 no.3
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    • pp.278-284
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    • 2006
  • The popularity of the diesel engine revolves around its fuel efficiency, reliability, and durability compared to the gasoline engine. However, the main disadvantage of diesel engine is the emission of particulate matter (PM) which is known as carcinogenic substance. Therefore recent progress in engine management and after-treatment systems has led to great improvement to satisfy strict emission regulations. To comply with powerful environment regulations, this study is focused on the decrease of PM(soot) as to increase significantly exhaust temperature. Therefore, HC injection is used as the method to go to the PM regeneration temperature in front of filters composed of diesel oxidation catalyst(DOC) and diesel particulate filter(DPF). And especially, LPG is used because it has good chemical reactions with exhaust. In this study, we could manufacture the test bench thought LPG injection - with which soot can be decreased-, construct 3 kinds of database(DB) according to quantity of temperature to decide the LPG injection quantity and develop DPF ECU algorithm.

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Studies on the Modeling of the Preparation of the C/SiC Composite for catalyst support by CVI (화학증기침투에 의한 촉매지지체용 C/SiC 복합체 제조에 관한 수치모사 연구)

  • 이성주;김미현;정귀영
    • Composites Research
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    • v.13 no.4
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    • pp.33-41
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    • 2000
  • In this research, the mathematical modeling of the formation of SiC layer on the activated carbon was studied to improve the durability and the oxidation resistance of catalyst supports. SiC layer on the activated carbon was formed by permeating SiC from dichlorodimethylsilane(DDS) into pores and depositing while the porous structure was kept. The best conditions of manufacturing the support were found by studying the characteristics of SiC/C which was modelled under various deposition conditions. Changes of the amount of deposition, the pore diameter, the surface area with time were obtained by simulating convection, diffusion and reaction in an isothermal reactor at a steady state. The uniform deposition in the pores of samples was obtained at a lower concentration of the reactant and a lower pressure. Additionally, it was observed that the pore diameter and the surface area have points of inflection at certain times of deposition, because deposition occurred on the inside surface of the pore at first and then on the outside surface of the particle.

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Effect of Number of Shutdown on the Decrease of Performance in PEM Water Electrolysis (PEM 수전해에서 정지횟수가 성능 감소에 미치는 영향)

  • Cheunho Chu;Jongwon Yang;Ilchai Na;Yoonjin Park
    • Korean Chemical Engineering Research
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    • v.61 no.2
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    • pp.202-207
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    • 2023
  • In the case of driving water electrolysis by receiving surplus electricity from solar and wind power generation, operation and stopping must be repeated according to weather fluctuations. When the PEMWE(Polymer Electrolyte Membrane Water Electrolysis) is driven and stopped, the PEM fuel cell is in the same state as the PEM fuel cell due to the residual hydrogen and oxygen, and the high potential of the water electrolysis formed during operation is highly likely to cause degradation of the electrode and membrane even during stopping. In this study, in order to check how much degradation of the electrode and membrane progresses during the repeated driving/shutdown process of PEM water electrolysis, the performance decrease was measured by changing the number of driving/shutdown for 144 hours. Changes in electrode catalyst active area, hydrogen permeability and fluorine emision rate of membranes were analyzed to measure changes in the properties of electrodes and polymer membranes. Overall, the PEMWE performance decreased as the number of stops increased. When stopped 5 times in 144 hours, the IrOx catalyst activity decreased by more than 30%, and the hydrogen permeability increased by 80%, confirming that both the electrode and the membrane were deteriorated.

Study on Effects of Ni/Al2O3 Catalysts Added with Mo on Durability Improvement in Steam Reforming Reactions (Mo를 첨가한 Ni/Al2O3 촉매의 수증기 개질반응에서의 내구성 증진 특성연구)

  • Won, Jong Min;Park, Gi Woo;Lee, Jin Woo;Hong, Sung Chang
    • Korean Chemical Engineering Research
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    • v.54 no.4
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    • pp.560-567
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    • 2016
  • In this study, we characterized steam reforming reactions and surface of $Ni/Al_2O_3$ catalysts. Ni-Mo based catalysts were prepared by loading Mo as the co-catalyst and reaction activities of the Ni-Mo based catalysts were compared with those of Ni-based catalysts. Through the $H_2$-TPR and XPS analysis it was confirmed that this characteristic efficiency. $O_2$-TPO analysis was performed to examine the deposition characteristics, bonding structures and evaporation characteristics of carbon deposited on the surface of catalysts after long run experiments were performed for steam reforming reactions. As the results, it was found that durability was improved in Ni-Mo based catalysts inhibiting formation of graphitic carbon species which reduced reaction activities of the catalysts by strongly interacting with Ni in the steam reforming reaction.

Effect of Vanadium Oxide Loading on SCR Activity and $SO_2$ Resistance over $TiO_2$-Supported $V_2O_5/TiO_2$ Commercial De-NOx Catalysts (상용 $V_2O_5/TiO_2$ 촉매의 바나듐 함량이 SCR 반응성과 $SO_2$ 내구성에 미치는 영향)

  • Park, Kwang Hee;Cha, Wang Seog
    • Applied Chemistry for Engineering
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    • v.23 no.5
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    • pp.485-489
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    • 2012
  • We investigated vanadium (V) loading effects on selective catalytic reduction (SCR) activity and $SO_2$ resistance using commercial SCR catalysts applied on a power plant and incinerator with different amounts of V loading. These catalysts were characterized using XRD, Raman, ICP, BET analysis and found to contain $TiO_2$ (anatase) supported $V_2O_5$ added $WO_3$ and $SiO_2$. The SCR activity of the catalysts increased by increasing either the $V_2O_5$ or the $WO_3$ loading amounts; the SCR activity of the catalysts added $WO_3$ is higher than that of $WO_3$-free catalysts. As the V loading amount in the catalyst increased, the $SO_2$ durability decreased. The $V_2O_5$ supported $TiO_2$ catalyst added $WO_3$ and $SiO_2$ inhibits the deactivation process by $SO_2$. The $SO_2$ resistance of catalysts added $SiO_2$ is higher than that of catalysts added $WO_3$.

Synthesis of CoFe2O4 Nanoparticles as Electrocatalyst for Oxygen Evolution Reaction (산소 발생 반응 용 전기화학촉매로 사용되는 CoFe2O4 나노 입자 합성 및 특성 분석)

  • Lee, Jooyoung;Kim, Geulhan;Yang, Juchan;Park, Yoo Sei;Jang, Myeong Je;Choi, Sung Mook
    • Journal of the Korean Electrochemical Society
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    • v.23 no.4
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    • pp.97-104
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    • 2020
  • One of the main challenges of electrochemical water splitting technology is to develop a high performance, low cost oxygen-evolving electrode capable of substituting a noble metal catalyst, Ir or Ru based catalyst. In this work, CoFe2O4 nanoparticles with sub-44 nmsize of a inverse spinel structure for oxygen evolution reaction (OER) were synthesized by the injection of KNO3 and NaOH solution to a preheated CoSO4 and Fe(NO3)3 solution. The synthesis time of CoFe2O4 nanoparticles was controlled to control particle and crystallite size. When the synthesis time was 6 h, CoFe2O4 nanoparticles had high conductivity and electrochemical surface area. The overpotential at current denstiy of 10 mA/㎠ and Tafel slope of CoFe2O4 (6h) were 395 mV and 52 mV/dec, respectively. In addition, the catalyst showed excellent durability for 18 hours at 10 mA/㎠.