• Title/Summary/Keyword: metal desorption

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Oxidation of Ethylbenzene Using Nickel Oxide Supported Metal Organic Framework Catalyst

  • Peng, Mei Mei;Jeon, Ung Jin;Ganesh, Mani;Aziz, Abidov;Vinodh, Rajangam;Palanichamy, Muthiahpillai;Jang, Hyun Tae
    • Bulletin of the Korean Chemical Society
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    • v.35 no.11
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    • pp.3213-3218
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    • 2014
  • A metal organic framework-supported Nickel nanoparticle (Ni-MOF-5) was successfully synthesized using a simple impregnation method. The obtained solid acid catalyst was characterized by Powder X-ray diffraction (XRD), scanning electron microscopy (SEM), nitrogen adsorption-desorption and thermogravimetric analysis (TGA). The catalyst was highly crystalline with good thermodynamic stability (up to $400^{\circ}C$) and high surface area ($699m^2g^{-1}$). The catalyst was studied for the oxidation of ethyl benzene, and the results were monitored via gas chromatography (GC) and found that the Ni-MOF-5 catalyst was highly effective for ethyl benzene oxidation. The conversion of ethyl benzene and the selectivity for acetophenone were 55.3% and 90.2%, respectively.

Hydrogen Absorption by Laves Phase Related BCC Solid Solution Alloys

  • Akiba, Etsuo
    • Journal of Hydrogen and New Energy
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    • v.8 no.3
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    • pp.101-109
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    • 1997
  • We propose a new concept of hydrogen absorbing alloy, "Laves phase related BCC solid solution". It was firstly found among the phases tormed in multicomponent nominal $AB_2$ alloys which consisted of Zr and Ti for the A metal site and 5A, 6A and 7A transition metals for the B metal sites. In these alloys a BCC solid solution often coexisted with a Laves phase. It showed stability of hydrides and reaction kinetics almost identical to intermetallics such as Laves phase alloys. We prepared an almost pure "Laves phase related BCC solid solution" and found that it had a large hydrogen capacity (more than 2 mass%) and fast hydrogen absorption and desorption kinetics at ambient temperature and pressure. This new hydrogen absorbing alloy may open a new era of hydrogen related application such as hydrogen vehicles.

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$H_2$ sensor for detecting hydrogen in DI water using Pd membrane (발전기 스테이터의 냉각코일에 pinhole 발생을 검지 할 수 있는 수소센서 개발)

  • Choi, Sie-Young
    • Proceedings of the KIEE Conference
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    • 1999.11b
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    • pp.442-445
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    • 1999
  • In this work, to detect of hydrogen in DI water in the generator area of nuclear power plants was fabricated Pd/Pt gate MISFET sensor using Pd membrane. $H_2$ permeation through Pd accounts for external mass transfer, surface adsorption and desorption, transitions to and from the bulk metal, and diffusion within the metal. The identification of pinholes in the generator area of plant is an important safety consideration, as hydrogen build-up gives rise to explosion. For this type of application the sensor needs to be isolated in DI water, accordingly, a Pd membrane was used to separate the DI water. The hydrogen in the DI water was then absorbed on the Pd thin film and diffused into the oil through the thin film. The Pd/Pt gate MISFET sensor, encapsulated by oil, will thereby detect permeated hydrogen.

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The Studies on the Simultaneous Removals of NOx and SOx from Stationary Sources by using Perovskite type Catalysts (페로브스카이트형 촉매계를 이용한 고정원 배가스로부터의 NOx 와 SOx의 동시제거 기술에 관한 연구)

  • Lee, Byong-Yong;Choung, Suk-Jin
    • Proceedings of the KIEE Conference
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    • 1996.11a
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    • pp.475-479
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    • 1996
  • At present studies, we are going to suggest the new type of Perovskite derived catalysts which modify the defects of transition metals impregnated. Perovskite type catalyst is a typical mixed metal oxides, and there are "defect"s (from like that oxygen, cation, crystallic structure) were made by difference from composition, preparing method and so forth. And because this, its electro-magnetic character could be much changed. By using this phenomena, it could utilize the modification of adsorption/desorption characters as well as the catalytic activities in NOx reduction. Because perovskite type catalyst can exchange the metal of the each lattice site freely and it is possible to represent the peculiar.

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Involvement of Lipopolysaccharide of Bradyrhizobium japonicum in Metal Binding

  • Oh, Eun-Taex;Yun, Hyun-Shik;Heo, Tae-Ryeon;Koh, Sung-Cheol;Oh, Kye-Heon;So, Jae-Seong
    • Journal of Microbiology and Biotechnology
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    • v.12 no.2
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    • pp.296-300
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    • 2002
  • Bacterial cell surface components are the major factors responsible for pathogenesis and bioremediation. In particular, the surface of a Gram-negative bacterium cell has a variety of components compared to that of a Gram-positive cell. In our previous study, we isolated an isogenic mutant of Bradyrhizobium japonicum, which exhibited altered cell surface characteristics, including an increased hydrophobicity. Polyacrylamide gel electrophoretic analysis of the lipopolysaccharide (LPS) in the mutant demonstrated that the O-polysaccharide part was completely absent. Meanwhile, a gel permeation chromatographic analysis of the exopolysaccharide (EPS) in the mutant demonstrated that it was unaltered. Since LPSs are known to have several anion groups that interact with various cation groups and metal ions, the mutant provided an opportunity to examine the direct role of LPS in metal binding by B. japonicum. Using atomic absorption spectrophotometry, it was clearly demonstrated that LPS was involved in metal binding. The binding capacity of the LPS mutant to various metal ions $(Cd^{2+},\;Cu^{2+},\;Pb^{2+},\;and\;Zn^{2+})$ was 50-70% lower than that of the wild-type strain. Also, through an EPS analysis and desorption experiment, it was found that EPS and centrifugal force had no effect on the metal binding. Accordingly, it would appear that LPS molecules on B. japonicum effect the properties, which precipitate more distinctly metal-rich mineral phase.

Adsorption and Storage of Natural Gas by Nanoporous Adsorbents (나노세공체 흡착제에 의한 천연가스의 흡착 및 저장)

  • Jhung, Sung Hwa;Chang, Jong-San
    • Applied Chemistry for Engineering
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    • v.20 no.2
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    • pp.117-125
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    • 2009
  • In order to utilize natural gas (NG), one of the clean energy sources in next-generation, as a fuel for vehicles, it is important to store natural gas with high density. To store NG by adsorption (ANG) at room temperature and at relatively low pressure(35~40 atm) is safe and economical compared with compressed NG and liquefied NG. However, so far no adsorbent is reported to have adsorption capacity suitable for commercial applications. Nanoporous materials including metal-organic frameworks can be potential adsorbents for ANG. In this review, physicochemical properties of adsorbents necessary for high adsorption capacity are summarized. Wide surface area, large micropore volume, suitable pore size and high density are necessary for high energy density. Moreover, low adsorption-desorption energy, rapid adsorption-desorption kinetics and high delivery are needed. Recently, various efforts have been reported to utilize nanoporous materials in ANG, and it is expected to develop a nanoporous material suitable for ANG.

A Study on the Analytical Errors of Non-proficient Laboratories Participated in Quality Control Program (작업환경측정기관의 정도관리를 통한 분석능력이 미흡한 기관들의 분석오차 유발요인에 관한 고찰)

  • Park, D.W.;Shin, Y.C.;Park, S.H.;Lee, N.R.;Oh, S.M.;Yoon, C.S.;Paik, N.W.
    • Journal of Korean Society of Occupational and Environmental Hygiene
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    • v.4 no.1
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    • pp.96-102
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    • 1994
  • Factors affecting non-proficient analytical ability were compared and evaluated by rating of laboratories and round. Analyst Indices between proficient and non-proficient participants were different. Coefficients of determination($R^2$) for standard of toluene, xylene and trichloroethylene of the 4th round between some proficient and non-proficient participants were significantly different(p<0.05). But, there was no difference in the 5th round. Average desorption efficiency of non-proficient participants was 88%-98%, which was lower than 96%-100% of some randomly selected proficient participants. Also non-proficient participants have a large variance of desorption efficiency, 11.79-19.69%. In the 5th round, desorption efficiency of metyl iso-butyl ketone(MIBK) reported by all participants was lower than 90% tested by NIOSH and especially low compared to other analytes. Participants evaluated to be non-proficient in the metal part have 85%-100.84% of average recovery, which was larger variance than 98% of some proficient participants. Although it is difficult to find quantitatively factors causing non-proficiency in analytical ability, pretreatement techniques and experience of analyst seems to be more important factors to produce accurate analytical result.

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Investigation of Cadmium and Zinc Interactions in Soils using Desorption Isotherms

  • Lee, Jin-Ho;Doolittle, James J.
    • Korean Journal of Environmental Agriculture
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    • v.25 no.2
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    • pp.157-163
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    • 2006
  • Investigation of Cd and Zn availability in four different soils as affected by the interactions of these two heavy metals was conducted using the metal desorption quantity-intensity (Q/I) isotherms. The soils were artificially contaminated with proper concentrations of Cd and Zn as $CdSO_4\;and\;ZnSO_4$ solutions. DTPA (diethylene triamine pentaacetic acid) - extractable and water-extiactable Cd or Zn from the soils were used as $Q_{Cd}\;or\;Q_{Zn}\;and\;I_{Cd}\;or\;I_{Zn}$ factors, respectively. The coefficient of determination for Cd and Zn desorption Q/I linear regression in the soils ranged from 0.947 to 0.999, which indicated that Q and I factors were closely correlated. The buffering capacity of Cd, $BC_{Cd}$, in the soils decreased with increasing Zn treatments, and the $BC_{Cd}$ values were ranged between 205.8 and 2255.6. The decreases of $BC_{Cd}$ values were mainly dependent upon the increases of $I_{Cd}$ factors. However, Zn buffering capacity. $BC_{Zn}$ decreased with increasing Cd treatments in acidic soils, and increased in neutral and calcareous alkaline soils. The $BC_{Cd}$ values were ranged from 143.2 to 6158.0. The values of $BC_{Zn}$ as influenced by the treatments of Cd were also controlled by the solubility of water-extractable Zn, $I_{Zn}$ factor. The solubility of water-extractable Cd and Zn was significantly dependent upon the changes of soil pH that were impacted by the treatment of Zn and Cd, respectively. Also, the availability of Cd was higher than Zn availability in the acidic and neutral soils, but Zn was higher than Cd in the calcareous alkaline soil.

Thermal and Photochemistry of Methyl Iodide on Ice Film Grown on Cu(111)

  • Sohn, Young-Ku;White, John M.
    • Bulletin of the Korean Chemical Society
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    • v.30 no.7
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    • pp.1470-1474
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    • 2009
  • Thermal and photochemistry of methyl iodide ($CH_3I)\;adsorbed\;on\;D_2O$ ice film on Cu(111) at 100 K were studied using temperature-programmed desorption (TPD) time-of-flight mass spectrometry (TOF-MS), X-ray and ultraviolet photoelectron spectroscopies. On the basis of TPD, multilayer and monolayer $CH_3I$ molecules desorb from $D_2O$ ice layer at 120 and 130 K, respectively. Photo-irradiation at 100 K exhibits dramatic changes in the TPD and I $3d_{5/2}\;XPS\;of\;CH_3I$ on ice film, due to a dramatic dissociation of $CH_3I$. The dissociation is likely activated by solvated electrons transferred from the metal substrate during photo-irradiation. No other photo-initiated reaction products were found within our instrumental detection limit. During photo-irradiation, the $CH_3I$, $CH_3$ and I could be trapped (or solvated) in ice film by rearrangement (and self-diffusion) of water molecules. A newly appeared parent molecular desorption peak at 145 K is attributed to trapped $CH_3I$. In addition, the $CH_3$ and I may diffuse through ice and chemisorb on Cu(111), indicated by TPD and I $d_{5/2}$ XPS taken with photo-irradiation time, respectively. No molecular ejection was found during photo-irradiation at 100 K. The work functions for $CH_3I/Cu(111),\;D_2O/Cu(111)\;and\;CH_3I/D_2$O/Cu(111) were all measured to be about 3.9 eV, 1.0 eV downward shift from that of clean Cu(111).

Biosorption of Pb and Cr by using Sargassum sagamianum (비틀대모자반, Sargassum sagamianum을 이용한 Pb 및 Cr 생체흡착 및 회수)

  • SUH Kuen-Hack;AHN Kab-Hwan;LEE Hack-Sung;LEE Hwae-Geon;CHO Jin-Koo;HONG Yong-Ki
    • Korean Journal of Fisheries and Aquatic Sciences
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    • v.32 no.4
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    • pp.399-403
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    • 1999
  • Biosorption of Pb and Cr to Sargassum sagamianum was evaluated in the various conditions. An adsorption equilibrium was reached in about 15 min. for Pb and Cr. The uptake capacity was 224.5 mg Pb/g biomass and 77.5 mg Cr/g biomass, respectively. The adsorption parameters for Pb and Cr were determined according to Langmuir and Freundlich model. Biosorption of Pb and Cr was increased with an increase in pH value. Pb and Cr adsorbed by S. sagamianum could be recovered by desorption process with 0.1M HCl, 0.1M $HNO_3$ and 0.1M EDTA and the efficiency of Pb desorption was above $90\%$, whereas the efficiency of Cr desorption was below $51\%$.

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