• 제목/요약/키워드: Hydrogen Adsorption

검색결과 436건 처리시간 0.028초

STM Study on c(4$\times$4) Reconstruction of Si(100)

  • Maeng, Jae-Yeol;Kim, Sehun
    • 한국진공학회:학술대회논문집
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    • 한국진공학회 2000년도 제18회 학술발표회 논문개요집
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    • pp.151-151
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    • 2000
  • We have studied the atomic structure of Si(100)-c(4$\times$4) reconstruction using scanning tunneling microscopy(STM). The c(4$\times$4) reconstruction can be formed by annealing the hydrogen exposured surface at temperatures between 850 and 960 K. At this temperature ranges, adsorbed hydrogen atoms are all desorbed. Therefore, the c(4$\times$4) reconstruction is due to the Si dimers on surface. The filled and empty state images of the STM were interpreted in terms of Si dimers in c(4$\times$4) primitive cell forming the reconstruction. Based on the STM images and hydrogen adsorption experiment on c(4$\times$40 surface, we suggest that Si dimers in c(4$\times$40 unit cell are perpendicular ad-dimer to the underlying Si dimer rows.

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Fundamentals of Underpotential Deposition : Importance of Underpotential Deposition in Interfacial Electrochemistry

  • Lee Jong-Won;Pyun Su-Il
    • 전기화학회지
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    • 제4권4호
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    • pp.176-181
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    • 2001
  • 본 논문은 계면 전기화학에서의 underpotential deposition (UPD)의 중요성에 초점을 맞추어 UPD의 기본원리에 대하여 다루었다. 우선 underpotential shift와 electrosorption valency에 대한 설명과 함께 UPD의 기본개념을 기술하였다. 다음으로 금속표면에서의 수소발생 또는 금속내부로의 수소흡수 반응 이전에 관찰되는 수소의 UPD를 설명하였고, 특히 금속 표면에서의 흡착위치와 Pd으로의 흡수기구에 대하여 중점적으로 기술하였다. 마지막으로, 계면 전기화학의 여러 분야에서 UPD와 관련된 중요한 인자들을 응용적인 측면에서 간략히 설명하였다.

금속담지된 $TiO_2$ 나노튜브를 활용한 Cr(VI)환원의 광화학적 효율 연구 (Study on Photocatalytic Cr(VI) Reduction with Metal Deposited Anodized $TiO_2$ Tube)

  • 허아영;이창하;박민성;심은정;윤재경;주현규
    • 한국수소및신에너지학회논문집
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    • 제21권4호
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    • pp.301-306
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    • 2010
  • The present work is performed to photocatalytically reduce Cr(VI) by means of metal deposited anodized $TiO_2$ tubes, which are prepared by anodization of Ti foil followed by metal deposition. Stably immobilized photo-reactive materials are favored in the field of detoxification in a conventional aqueous medium, preventing gradual loss of efficiency and process malfunction due to detachment of the materials. The prepared samples are characterized by SEM, TEM, EDAX, and photocurrent. The metal deposited-$TiO_2$ electrode shows higher efficiency for Cr(VI) reduction (ca. 20%) and higher ability for adsorption (4~5 times) than pure one.

수냉식 방열을 이용한 연료전지용 PROX 반응기의 성능에 관한 실험적 연구 (Experimental Study on the Preferential Oxidation Reactor Performance Using a Water Cooling Heat Removal for Polymer Electrolyte Membrane Fuel Cell)

  • 김진산;조태현;구본찬;이도형
    • 한국수소및신에너지학회논문집
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    • 제27권5호
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    • pp.503-509
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    • 2016
  • Fuel cell is a device for producing electricity by using the hydrogen produced by the fuel processor. At this time, CO is also created by the fuel processor. The resulting CO enters the stack where is produce electricity and leads to the adsorption of anode catalyst, finally the CO poisoning occurs. Stack which occurred CO poisoning has a reduction in performance and shelf life are gradually fall because they do not respond to hydrogen. In this paper, experiments that using a PROX reactor to prevent CO poisoning were carried out for removing the CO concentration to less than 10ppm range available in the fuel cell. Furthermore experiments by the PROX reaction was designed and manufactured with a water-cooling heat exchange reactor to maintain a suitable temperature control due to the strong exothermic reaction.

코크스 오븐 가스(COG)를 이용한 수소 및 합성가스 제조 기술 개발 동향 분석 (A Review of Technology Development Trend for Hydrogen and Syngas Production with Coke Oven Gas)

  • 최종호
    • 한국산업융합학회 논문집
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    • 제25권6_3호
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    • pp.1247-1260
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    • 2022
  • The steel industry accounts for about 5% of the total annual global energy consumption and more than 6% of the total anthropogenic carbon dioxide emissions. Therefore, there is a need to increase energy efficiency and reduce greenhouse gas emissions in these industries. The utilization of coke oven gas, a byproduct of the coke plant, is one of the main ways to achieve this goal. Coke oven gas used as a fuel in many steelmaking process is a hydrogen-rich gas with high energy potential, but it is commonly used as a heat source and is even released directly into the air after combustion reactions. In order to solve such resource waste and energy inefficiency, several alternatives have recently been proposed, such as separating and refining hydrogen directly from coke oven gas or converting it to syngas. Therefore, in this study, recent research trends on the separation and purification of hydrogen from coke oven gas and the production of syngas were introduced.

탄산나트륨 첨착섬유활성탄을 이용한 황화수소의 제거 (Removal of Hydrogen Sulfide by Using Sodium Carbonate Impregnated Activated Carbon Fiber)

  • 정헌석;원용선;;;임준혁
    • 청정기술
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    • 제23권1호
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    • pp.113-117
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    • 2017
  • 본 연구에서는 섬유활성탄에 탄산나트륨을 첨착제로 이용하여 탄산나트륨 첨착섬유활성탄을 제조하고 동일조건에서 제조한 탄산나트륨 첨착입상활성탄과 황화수소 제거 성능을 비교한 후 그 활용가능성을 검토하고자 하였다. 첨착용액의 농도와 첨착시간을 변수로 하여 탄산나트륨 첨착섬유활성탄과 탄산나트륨 첨착입상활성탄의 흡착능을 구하였는데 먼저 두 경우 모두 첨착용액의 농도에 비례하여 탄산나트륨의 첨착되는 양도 증가하나 3 wt%이상에서는 기공충전(pore filling) 현상으로 첨착양에 변화가 없었다. 따라서 황화수소 제거를 위한 탄산나트륨 첨착섬유활성탄과 탄산나트륨 첨착입상활성탄의 제조시 최적의 탄산나트륨 용액 농도는 3 wt%인 것으로 판단되었다. 또한 탄산나트륨 첨착섬유활성탄의 경우 탄산나트륨 첨착을 위한 담지시간이 탄산나트륨 첨착입상활성탄에 비하여 2배 가까이 빠른 것으로 나타났다. 황화수소 제거효율은 탄산나트륨 첨착섬유활성탄이 탄산나트륨 첨착입상활성탄에 비하여 30% 이상 증가하였고 이는 비표면적의 측정결과로 설명되었다. 결과적으로 향상된 비표면적을 가진 섬유활성탄에 황화수소와 화학적으로 반응하는 탄산나트륨을 첨착하여 제조상 시간적 이점과 향상된 황화수소 흡착능을 확인할 수 있었다.

나노다공체 물성 측정을 위한 극저온(20K) 수소 BET 개발 및 응용 (Development of a Cost-Effective 20K Hydrogen BET Measurement for Nanoporous Materials)

  • 박재우;오현철
    • 한국재료학회지
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    • 제27권9호
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    • pp.466-470
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    • 2017
  • With the matters of climate change, energy security and resource depletion, a growing pressure exists to search for replacements for fossil fuels. Among various sustainable energy sources, hydrogen is thought of as a clean energy, and thus efficient hydrogen storage is a major issue. In order to realize efficient and safe hydrogen storage, various porous materials are being explored as solid-states materials for hydrogen storage. For those purposes, it is a prerequisite to characterize a material's textural properties to evaluate its hydrogen storage performance. In general, the textural properties of porous materials are analyzed by the Brunauer-Emmett-Teller (BET) measurement using nitrogen gas as a probe molecule. However, nitrogen BET analysis is sometimes not suitable for materials possessing small pores and surfaces with high curvatures like MOFs because the nitrogen molecule may sometimes be too large to reach the entire porous framework, resulting in an erroneous value. Hence, a smaller probe molecule for BET measurements (such as hydrogen) may be required. In this study, we describe a cost-effective novel cryostat for BET measurement that can reach temperatures below the liquefaction of hydrogen gas. Temperature and cold volume of the cryostat are corrected, and all measurements are validated using a commercial device. In this way, direct observation of the hydrogen adsorption properties is possible, which can translate directly into the determination of textural properties.

활성탄의 표면처리에 의한 천연가스 흡장 (Natural Gas Sorption Using Activated-Carbon with Surface Treatment)

  • 윤석민;김주완;임지선;김신동;홍지숙;서정권;이영석
    • 한국수소및신에너지학회논문집
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    • 제17권4호
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    • pp.434-439
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    • 2006
  • In this study, activated carbon(ACs) have been modified by nitric acid and heat-treatment. The surface and structure properties of ACs were determined by BET surface area, FT-IR pH and acid/base value. The changes in pore structure and surface properties of these modified ACs were correlated with natural gas adsorption which measured by volumetric apparatus at $0^{\circ}C$ and $25^{\circ}C$. The pore textural properties of activated carbon was also characterized by nitrogen adsorption at 77 K. Specific surface area and micropore volume of them were calculated by Langmuir equation and Horvath-Kawazoe method, and chemical properties of surface were measured by FT-IR and titration of acid and base solutions. Pore texture of activated carbons after treatments were not significantly changed. Total acidity increased and basicity of samples decreased. however the basicity increased with heat treatment. The methane adsorption of ACs become different depending on the acid/base value of samples.

Extracting Gold from Pyrite Roster Cinder by Ultra-Fine-Grinding/Resin-in-Pulp

  • Guo, Bingkun;Wei, Junting
    • 대한전자공학회:학술대회논문집
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    • 대한전자공학회 2001년도 The 6th International Symposium of East Asian Resources Recycling Technology
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    • pp.337-341
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    • 2001
  • A new method to extract gold from pyrite roster cinder, which combines ultra-fine-grinding with resin-in-pulp, has been studied in this paper. Compared with traditional leaching technology, it can short leaching time, avoid complex filter process, lower sodium cyanide consumption and increase gold recovery by 35%. During leaching, aluminium oxide ball was used as stirred medium, hydrogen peroxide as leaching aid and sodium hexametaphosphate as grinding aid. With the high efficiency and chemistry effect of ultra-fine-grinding, the leaching process was developed and the gold leaching rate may reach 88%. With AM-2 Б resin as abosorber and sulfocarbamide (TU) as eluent, gold was recovered from cyanide pulp by resin-in-pulp. AM-2 Б resin has good adsorbability in cyanide solution(pH=10). It was easy to elude gold from the loaded resin with 0.1㏖/L cholhydric acid and 1㏖/L sulfocabamide. The effect of contact time, temperature and acidity etc. on the gold absorption had been examined with static methods. The results showed that the adsorption and desorption of gold could both reach over 98%. The effects of flow rate of solution on dynamic adsorption and elution of gold had been examined with dynamic methods. Breakthrough curve and elution curve had been drawn in this paper. A mild condition was determined through a number of experiments: leaching time 2 hours, liquid solid ratio 4:1, sodium cyanide 3kg/t, hydrogen peroxide 0.05%, sodium hexametaphosphate 0.05%; adsorption time 30 minutes, temperature 10-3$0^{\circ}C$, resin($m\ell$) solid(g) ratio 1:10, eluent resin ratio 10-20:1, velocity of eluent $1.5m\ell$/min. Under the mild condition, the gold recovery may reach 85%.

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Layer Silicate에 지지된 양이온상에서 일어나는 Alkyl Ketones의 흡착기구. 水酸基의 Link 形成理論 (Adsorption Mechanism of Alkyl Ketones on Cation Supported by Layer Silicate. Link Formation of Hydroxyl Group)

  • 김종탁;손종락
    • 대한화학회지
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    • 제17권4호
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    • pp.247-255
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    • 1973
  • $Li^{+},\;Na^{+},\;K^{+}, Ca^{2+},\;Ni^{2+},\;Al^{3+}$, 과 $F^{3+}$의 陽이온을 포화시킨 Wyoning montmorillonite에 acetone, methyl-ethyl ketone. diethyl ketone을 加熱用 i.r. gas cell 內에서 各各 다른 壓力아래 吸着시켜 $4000{\sim}1200cm^{-1}$에서spectra를 얻었다.두가지 형태의 C=O결합변화가$1713cm^{-1}$$1690cm^{-1}$ 나타났으며 이들은 陽이온의 水酸基 및 吸着水와 그리고 表面水酸基와 水素結合을 일으키는 결과로 나타났다. OH 吸收 spectra의 强度는 陽이온의 水酸基의 resonance 理論을 뒷받침해 주었다. coordinate bond를 일으키는 경향은 計算한 C=O기의 酸素의 formal charge의 크기와 잘 맞았다.

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