• Title/Summary/Keyword: Stirring energy

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Fabrication of Electrospun Si-Zr-C Fibers by Electron Beam Irradiation (전자선 조사를 이용한 전기방사된 Si-Zr-C 섬유의 제조)

  • Seo, Dong Kwon;Jeun, Joon Pyo;Kim, Hyun Bin;Kang, Phil Hyun
    • Journal of Radiation Industry
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    • v.4 no.3
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    • pp.265-269
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    • 2010
  • Silicon-based non-oxide ceramic carbide fiber is one of the leading candidate ceramic materials for engineering applications because of its excellent mechanical properties at high temperature and good chemical resistance. In this study, polycarbosilane(PCS) and zirconium butoxide were used as a precursor to prepare polyzirconocarbosilane (PZC) fibers. A polymer solution was prepared by dissolving PCS in zirconium butoxide (50/50 wt%). This solution was heated at $250^{\circ}C$ in a nitrogen atmosphere for 2 hour with stirring, and then dried in a vacuum oven for 48 hour. PZC fibers were fabricated using an electrospinning technique. The fibers were irradiated with an electron beam to induce structural crosslinking. Crosslinked PZC fibers were heat treated at $1,300^{\circ}C$ in a nitrogen atmosphere. The microstructures of PZC fibers were examined by SEM. Chemical structures of PZC fibers were examined by FT-IR and XRD. Thermal stability of PZC fibers was investigated by TGA.

Studies on the Preparation of $^{99m}TC$ Labelled Human Albumin Microsphere for Lung Scintigraphy (폐 신티그래피용 $^{99m}TC$ 표지 미소구형인 혈청 알부민의 제조에 관한 연구)

  • Park, Kyung-Bae;Awh, Ok-Doo;Kim, Jae-Rok
    • The Korean Journal of Nuclear Medicine
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    • v.23 no.1
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    • pp.63-69
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    • 1989
  • In order to develop technetium-99m-labelled human albumin microsphere (HAM) for lung scintigraphy, various experimemts such as preparation and fractionation of HAM, establishment of optimal labelling conditions, determination of radiochemical purity, stability test and biodistribution of $^{99m}Tc-HAM$ were carried out. HAM was prepared from the suspension of 1ml aqueous human serum albumin (25%) in 130 ml of olive oil at $130\sim135^{\circ}$ with vigorous stirring. The resulting HAM was fractionated with microsieve to get the desired particle size $(15\sim50\mu)$ and autoclaved for sterilizaiton. The HAM particles were treated with stannous chloride and the pH of the suspension was adjusted to $3.0\sim3.5$ with phosphate buffer. After freeze-drying the contents of single reaction vial containing 5 mg of HAM and 0.2 mg of $SnCl_2$ it was reacted with $Na^{99m}TcO_4$. The labelling yield was higher than 99.5% and the stability of $^{99m}Tc-HAM$ was high enough to maintain 99.1% of radiochemical purity up to 24 hours. Lung and liver uptake in mice was found to be 94% and 0.9%, respectively. Excellent rabbit and human lung scans were also obtained.

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Flow Analysis of the Environmental Chemical Reaction Processes at Power Plant in accordance with the Baffle Structure

  • Jeong, Yeon-Tae;Hur, Kwang-Beom;Gil, Joon-Woo
    • KEPCO Journal on Electric Power and Energy
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    • v.2 no.3
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    • pp.433-436
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    • 2016
  • In the area of environmental chemistry of power plant, flow analysis of the reactor with built-in impeller is a very important part from the perspective of the improvement of the efficiency of the entire process. As a wide range of methods are being proposed for the analysis of the flow pattern within the reactor, this study analyzed the flow within the reactor according to the baffle structure (height) installed on the internal wall of the reactor in order to improve the reaction efficiency through the inducing of the up and down stirring with the reactor. As the results of the execution of the flow analysis for each of a diverse range of cases by utilizing the Computational Fluid Dynamics (CFD) method, it was possible to confirm that the flow is markdely improved by inducing the up and down stirring among the reactants within the reactor if the baffle is elevated to the level below the water surface. In particular, as the results of the analysis of the general cases in which the baffle is elevated all 4 steps and the cases in which the baffle is elevated only 2 steps, elevating the baffle only 2 steps achieve the same effect as the elevating of the baffle by 4 steps. Therefore, it was possible to expect to improve the efficiency with out the need to increase the use of electric power substantially if the outcomes of this study is applied to the actual sites of power plants in the future.

Optimizing Nitrobenzene Synthesis Catalyzed by Sulfated Silica (SO4/SiO2) through Response Surface Methodological Approach

  • Aan Sabilladin;Aldino Javier Saviola;Karna Wijaya;Aulia Sukma Hutama;Mokhammad Fajar Pradipta;Wahyu Dita Saputri;Hilda Ismail;Budhijanto Budhijanto;Won-Chun Oh;Balasubramani Ravindran
    • Korean Journal of Materials Research
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    • v.34 no.7
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    • pp.341-354
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    • 2024
  • Today, the principles of green chemistry are being fundamentally applied in the chemical industry, such as the nitrobenzene industry, which is an essential intermediate for various commercial products. Research on the application of response surface methodology (RSM) to optimize nitrobenzene synthesis was conducted using a sulfated silica (SO4/SiO2) catalyst and batch microwave reactor. The nitrobenzene synthesis process was carried out according to RSM using a central composite design (CCD) design for three independent variables, consisting of sulfuric acid concentration on the silica (%), stirring time (min), and reaction temperature (℃), and the response variable of nitrobenzene yield (%). The results showed that a three-factorial design using the response surface method could determine the optimum conditions for obtaining nitrobenzene products in a batch microwave reactor. The optimum condition for a nitrobenzene yield of 63.38 % can be obtained at a sulfuric acid concentration on the silica of 91.20 %, stirring time of 140.45 min, and reaction temperature of 58.14 ℃. From the 20 experiments conducted, the SO4/SiO2 catalyst showed a selectivity of 100 %, which means that this solid acid catalyst can potentially work well in converting benzene to nitrobenzene.

Preparation and Characterization of Palladium Nanoparticles Supported on Nickel Hexacyanoferrate for Fuel Cell Application

  • Choi, Kwang-Hyun;Shokouhimehr, Mohammadreza;Kang, Yun Sik;Chung, Dong Young;Chung, Young-Hoon;Ahn, Minjeh;Sung, Yung-Eun
    • Bulletin of the Korean Chemical Society
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    • v.34 no.4
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    • pp.1195-1198
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    • 2013
  • Nickel hexacyanoferrate supported palladium nanoparticles (Pd-NiHCF NPs) were synthesized and studied for oxygen reduction reactions in direct methanol fuel cell. The NiHCF support was readily synthesized by a comixing of $Ni(OCOCH_3)_2$ and equimolar $K_3[Fe(CN)_6]$ solution into DI water under rigorous stirring. After the preparation of NiHCF support, Pd NPs were loaded on NiHCF via L-ascorbic acid reduction method at $80^{\circ}C$. Pd-NiHCF NPs were electrochemically active for oxygen reduction reaction in 0.1 M $HClO_4$ solution. X-ray absorption near edge structure analysis was conducted to measure the white line intensity of Pd-NiHCF to verify the OH adsorption. As a comparison, carbon supported Pd NPs exhibited same white line intensity. This study provides a general synthetic approach to easily load Pd NPs on porous coordination polymers such as NiHCF and can provide further light to load Pd based alloy NPs on NiHCF framework.

Study on a Phosphorylation of Rare Earth Nuclide (Nd) in LiCl-KCl-NdCl3 System using Li3PO4-K3PO4 (LiCl-KCl-NdCl3계에서 Li3PO4-K3PO4를 이용한 희토류 핵종(Nd) 인산화에 관한 연구)

  • Eun, Hee-Chul;Kim, Jun-Hong;Choi, Jung-Hoon;Cho, Yung-Zun;Lee, Tae-Kyo;Park, Hwan-Seo;Park, Geun-Il
    • Journal of Advanced Engineering and Technology
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    • v.6 no.2
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    • pp.125-129
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    • 2013
  • In the pyrochemcial process of spent nuclear fuel, it is necessary to separate rare earth nuclides from LiCl-KCl eutectic waste salt for radioactive waste reduction. This paper presents the phosphorylation of neodymium chloride in LiCl-KCl-NdCl3 system using Li3PO4-K3PO4 as a phosphorylation agent in a chemical reactor with pitched blade impellers. The phosphorylation test was performed changing operation temperature, stirring rate, and amount of phosphorylation agent. Neodymium chloride was effectively converted into neodymium phosphate (NdPO4). It was confirmed that more than 99 wt% of neodymium can be separated from LiCl-KCl-NdCl3 system using a phosphorylation method l

Preparation of Copper-coated Graphite Composite Powder by Hydrometallurgical Process (습식법에 의한 동-흑연 복합분말 제조)

  • 김동진;정헌생;윤기병
    • Journal of the Korean Crystal Growth and Crystal Technology
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    • v.3 no.1
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    • pp.75-84
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    • 1993
  • Copper coating on graphite powders was carried out by cementation process from copper sulfate solution. Effects of operation variables such as copper ion concentration, stirring speed, reaction time and temperature were investigated to obtain optimum conditions for continuous and uniform copper coating on graphite powders. The activation energy of the copper coating process was found to be 3. 59kcal/mole.

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A Study on Molten Salt Electrorefining of Uranium Metal Using Low Carbon Steel Cathode (저 탄소강 음극을 사용한 금속우라늄의 용융염 전해정련에 관한 연구)

  • Yang, Y.S.;Kang, Y.H.;Hwang, S.C.
    • Applied Chemistry for Engineering
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    • v.10 no.8
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    • pp.1119-1123
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    • 1999
  • In this paper, electrorefining of uranium metal was studied to develop pyrometallurgical processing technology in molten salt system. The reaction between uranium metal and $CdCl_2$ was taken about 3 hours and the uranium metal deposits were obtained in the form of dendrite grown on the cathode surface in every electrotransport experiment. The shapes of dendrite were changed according to the applied voltages. Current efficiency was decreased with the increase of current density. Deposition rate was not changed after 6 hours and its maxium was obtained at $100{\sim}150mA/cm^2$ of current density and about 75 rpm of stirring speed, respectively. Also, the current efficiency was increased with decrease of the pitch of spiral groove curved on cathode.

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Sulfuric Acid Leaching of Manganese from Ferromanganese Dust (황산에 의한 페로망간 집진분 중의 망간 침출)

  • Park, Suji;Sohn, Ho-Sang
    • Resources Recycling
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    • v.24 no.6
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    • pp.24-30
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    • 2015
  • The sulfuric acid leaching of ferromanganese dust was studied. The effect of acid concentration, reaction temperature, stirring rate, particle size and solid to liquid ratio on Mn and Fe extraction in the solution were investigated. It was found that the leaching rate of Mn and Fe increased with increasing reaction temperature and sulfuric acid concentration. Examination of data by shrinking core model suggested that the leaching rate is controlled by chemical reaction at the surface of particle. The activation energy for the leaching reaction of Mn and Fe were calculated to be 79.55 kJ/mol and 77.48 kJ/mol, respectively.

Evaluation of Design of Experiments to Develop MOF-5 Adsorbent for Acetylene Capture

  • Min Hyung Lee;Sangmin Lee;Kye Sang Yoo
    • Korean Chemical Engineering Research
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    • v.61 no.2
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    • pp.322-327
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    • 2023
  • A design of experiments was evaluated in optimizing MOF-5 synthesis for acetylene adsorption. At first, mixture design was used to optimize precursor concentration, terephthalic acid, zinc acetate dihydrate and N,N-dimethylformamide. More specifically, 13 conditions with various molar ratios were designed by extreme vertices design method. After preparing the samples, XRD, N2 physisorption and SEM analysis were performed for their characterization. Moreover, acetylene adsorption experiments were carried out over the samples under identical conditions. The optimal precursor composition for MOF-5 synthesis was predicted on a molar basis as follows: terephthalic acid : acetate dihydrate : dimethylformamide = 0.1 : 0.4 : 0.5. Thereafter, multi-level factorial design was designated to investigate the effect of synthesis reaction conditions such as temperature, time and stirring speed. By the statistical analysis of 18 samples designed, 4 reaction parameters were determined for additional adsorption experiments. Therefore, MOF-5 prepared under the synthesis time and temperature of 100 ℃ and 12 h, respectively, showed the maximum adsorption capacity of 15.1 mmol/g.