• 제목/요약/키워드: Bulk Reaction

검색결과 323건 처리시간 0.027초

MmNi4.5Al0.5의 수소화 반응특성 및 Temperature-Induced Cycling에 따른 수소화 반응속도의 변화에 관한 연구 (A Study on the Hydriding Reaction Characteristics and the Change of the Hydriding Reaction Rates of MmNi4.5Al0.5 during Temperature-Induced Cycling)

  • 김수령;이재영
    • 한국수소및신에너지학회논문집
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    • 제1권1호
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    • pp.1-8
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    • 1989
  • The hydriding kinetic mechanism and the change of the hydriding reaction rate of $MmNi_{4.5}Al_{0.5}$ during the thermally induced hydrogen absorption-desorption cycling are investigated. Comparison of the reaction rate data which are obtained by the pressure sweep method with the theoretical rate equations suggests that the hydriding rate controlling step has changed from the dissociative chemisorption of hydrogen molecules at the surface to the hydrogen diffusion through the hydride phase with the increase of the hydriding fraction. These hydriding kinetic mechanism is not changed during the cycling. However, the intrinsic hydriding reaction rate of $MmNi_{4.5}Al_{0.5}$ after 5500 cycles increases significantly comparing with the activated one. It is suggested that the change of the hydriding kinetic behavior due to intrinsic degradation of $MmNi_{4.5}Al_{0.5}$ can be interpreted as follows ; the formation of nickel cluster at the surface of the sample and the host metal atom exchange in bulk by thermal cycling.

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치과용(齒科用) 수산화(水酸化)칼슘 시멘트의 경화반응(硬化反應)에 관(關)한 적외선분석학적(赤外線分析學的) 연구(硏究) (AN INFRA-RED SPECTROPHOTOMETRIC STUDY OF THE REACTION IN CALCIUM HYDROXIDE DENTAL CEMENT)

  • 김중종;민병순;최호영;박상진
    • Restorative Dentistry and Endodontics
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    • 제10권1호
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    • pp.71-83
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    • 1984
  • The purpose of this study was to evaluate the transmission spectrum of the set calcium hydroxide dental cement (Dycal, L.D. Caulk Co. Milford, Del.) Cement was prepared for A T R spectra at a low powder-to-liquid ratio of 3.0gm/ml in order to retard the reaction and facilitate the manipulation of loading the cement into the cell. Spectra were recorded on an I R Spectrophotometer (MX-1, FT) at an agle of incidence of 55. The A T R cell was a RIIc Model TR5 with a hemisperical KRS-5 (Thallium-Bromide-Iodide). A spectrum was recorded within 3 minutes. Further spectra were recorded after 5,10,30 minutes and 1,5,24, 72 hours. The results were as follows; 1. The setting reaction between acid paste and base past would take place fastly within 10 minutes after mix, and that would be slow until 72 hours after mix. 2. In the set cements, some methyl salicylate and calcium hydroxide remained unreacted until 72 hours after mix. 3. The setting reaction and the reaction rate occuring at the surface and in the bulk cements were similar. 4. The chelates were bound together between calcium hydroxide and methyl salicylate.

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Reaction temperature dependence of MgB2 superconducting bulks using the different sizes of Mg raw powders

  • K.C., Chung
    • 한국초전도ㆍ저온공학회논문지
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    • 제24권4호
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    • pp.36-39
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    • 2022
  • Since the MgB2 superconductor is simply composed of two constituents of Mg and B, its performance can be monitored easily with the change of one ingredient compared to the other. With the powder size of B less than 100 nm, two different sizes of Mg powders are used to investigate the reaction temperature dependence of MgB2 bulk samples. In the range of 630-700℃ for the duration of 30 min., the un-reacted Mg is seen only at 630℃ with Mg powder size of <5 ㎛, whereas Mg traces are detected at all the temperature range with Mg powder size of <45 ㎛. The reaction temperature dependence of MgB2 superconducting transition temperature, Tc, shows little difference whether Mg powder size is large or small in this range except for the 630℃. It is worthy of notice that the critical current densities of MgB2 show higher performance with the small size of Mg compared to the large one at all field ranges. With the Mg powder size of <45 ㎛, flux pinning is enhanced with decreasing the reaction temperature, whereas flux pinning properties is quite similar in the Mg powder size of <5 ㎛ except for the 630℃, where Mg is left behind after the reaction.

헤테로폴리산 촉매의 산점 형성과 역할 (Formation and Role of Acid Sites of Heteropoly Acid Catalysts)

  • 송인규;이종국;송재천;이화영
    • 공업화학
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    • 제5권3호
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    • pp.431-437
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    • 1994
  • 에탄을 전화반응 및 MTBE (methyl t-butyl ether)분해반응을 통하여 헤테로폴리산 촉매가 지니는 표면 및 내부 산점의 역할과 형성에 대하여 살펴 보았다. 12-텅스토인산에서 에탄올 탈수반응을 수행할 경우 디에틸에테르는 표면산점에서 생성되며 에틸렌은 촉매 내부산점에서 생성된다. 물은 산점을 강화하는 역할을 하지만 유기염기의 경우 내부 산점을 약화시킨다. 금속염의 산점 형성은 결정수의 가수분해 혹은 금속의 부분적 치환에 따른 양성자에 기인하며 수소로 처리할 경우 산점이 재생되었다. 또한 산 특성 제어를 통하여 선택적 산화반응 촉매로서의 헤테로폴리산 설계가 가능하다.

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Ni 도핑을 통한 정방성이 높은 벌크 PbTiO3 세라믹 합성 (Fabrication of Bulk PbTiO3 Ceramics with a High c/a Ratio by Ni Doping)

  • 선정우;조재현;조욱
    • 한국전기전자재료학회논문지
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    • 제35권4호
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    • pp.407-411
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    • 2022
  • Bulk-sized PbTiO3 (PT), which is widely known as a high-performance ferroelectric oxide but cannot be fabricated into a monolithic ceramic due to its high c/a ratio, was successfully prepared with a high tetragonality by partially substituting Ni ions for Pb ions using a solid-state reaction method. We found that Ni-doped PT was well-fabricated as a bulk monolith with a significant c/a ratio of ~1.06. X-ray diffraction on as-sintered and crushed samples revealed that NiTiO3 secondary phase was present at the doping level of more than 2 at.%. Scanning electron microscopic study showed that NiTiO3 secondary phase grew on the surface of PT specimens regardless of the doping level possibly due to the evaporation of Pb during sintering. We demonstrated that an unconventional introduction of Ni ions into A-site plays a key role on the fabrication of bulk PT, though how Ni ion functions should be studied further. We expect that this study contributes to a further development of displacive ferroelectric oxides with a high c/a ratio.

Molecular characteristics of Escherichia coli from bulk tank milk in Korea

  • Yoon, Sunghyun;Lee, Young Ju
    • Journal of Veterinary Science
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    • 제23권1호
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    • pp.9.1-9.11
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    • 2022
  • Background: Escherichia coli, which causes subclinical or clinical mastitis in cattle, is responsible for transmitting antimicrobial resistance via human consumption of raw milk or raw milk products. Objectives: The objective of this study was to investigate the molecular characteristics of 183 E. coli from bulk tank milk of five different dairy factories in Korea. Methods: The molecular characteristics of E. coli such as serogroup, virulence, antimicrobial resistance, and integron genes were detected using polymerase chain reaction and antimicrobial susceptibility were tested using the disk diffusion test. Results: In the distribution of phylogenetic groups, group D was the most prevalent (59.6%) and followed by group B1 (25.1%). The most predominant serogroup was O173 (15.3%), and a total of 46 different serotypes were detected. The virulence gene found most often was fimH (73.2%), and stx1, fimH, incC, fyuA, and iutA genes were significantly higher in isolates of phylogenetic group B1 compared to phylogenetic groups A, B2, and D (p < 0.05). Among 64 E. coli isolates that showed resistance to at least one antimicrobial, the highest resistance rate was observed for tetracyclines (37.5%). All 18 integron-positive E. coli carried the integron class I (int1) gene, and three different gene cassette arrangements, dfrA12+aadA2 (2 isolates), aac(6')-Ib3+aac(6')-Ib-cr+aadA4 (2 isolates), and dfrA17+aadA5 (1 isolate) were detected. Conclusions: These data suggest that the E. coli from bulk tank milk can be an indicator for dissemination of antimicrobial resistance and virulence factors via cross-contamination.

N-methylpyrrolidine Alane 전구체를 사용한 Al 필름 합성 및 특성 분석 (Synthesis and Characterization of Al Film using N-methylpyrrolidine Alane)

  • 서문규
    • 한국전기전자재료학회논문지
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    • 제22권7호
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    • pp.549-554
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    • 2009
  • Al thin films were synthesized on TiN/Si substrate by MOCVD using N-methylpyrrolidine alane (MPA) precursor. Effects of substrate temperature, reaction pressure on the deposition rate, surface roughness and electrical resistivity were investigated. The early stage of Al thin film formation was analyzed by in-situ surface reflectivity measurement with a laser and photometer apparatus. From the Arrhenius plot of deposition rate vs. substrate temperature, it was found that the activation energy of surface reaction was 91.1kJ/mole, and the transition temperature from surface-reaction-limited region to mass-transfer-limited region was about $150^{\circ}C$. The growth rate increased with the reaction pressure, and average growth rates of $200{\sim}1,200nm/min$ were observed at various experimental conditions. Surface roughness of the film increased with the film thickness. The electrical resistivity of Al film was about $4{\mu}{\Omega}{\cdot}cm$ in the case of optimum condition, and it was close to the value of the bulk Al, $2.7{\mu}{\Omega}{\cdot}cm$.

에탄 열분해 반응이 동반된 관형 반응기에서의 열전달 및 화학반응 특성 연구 (THE CHARACTERISTICS OF HEAT TRANSFER AND CHEMICAL REACTION FOR THERMAL CRACKING OF ETHANE IN TUBULAR REACTOR)

  • 신찬영;안준
    • 한국전산유체공학회지
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    • 제21권1호
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    • pp.43-49
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    • 2016
  • Thermal cracking is commonly modeled as plug flow reaction, neglecting the lateral gradients present. In this paper, 2-dimensional computational fluid dynamics including turbulence model and molecular reaction scheme are carried out. This simulation is solved by means of coupled implicit scheme for stable convergence of solution. The reactor is modeled as an isothermal tube, whose length is 1.2 m and radius is 0.01 m, respectively. At first, The radial profile of velocity and temperature at each point are predicted in its condition. Then the bulk temperature and conversion curve along the axial direction are compared with other published data to identify the reason why discussed variations of properties are important to product yield. Finally, defining a new non-dimensional number, Effect of interaction with turbulence, heat transfer and chemical reaction are discussed for design of thermal cracking furnace.

Copolymerization of L-Lactide and ${\varepsilon}$-Caprolactone in Supercritical Fluid

  • Prabowo, Benedictus;Choi, Dong-Hoon;Kim, Soo-Hyun
    • Macromolecular Research
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    • 제17권8호
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    • pp.575-579
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    • 2009
  • Copolymerization of L-lactide and s-caprolactone initiated by tin (II) octoate (Sn(Oct)$_2$) was carried out in supercritical chlorodifluoromethane (R22) with varying reaction conditions (time and temperature) and amounts of monomer and catalyst, under a pressure of 250 bar. The optimum conditions were a reaction time of 10 h and a temperature of 130 $^{\circ}C$, which is similar to the temperature used in bulk copolymerization system. The conversion increased from 56% to 76% by increasing the reaction time from 1 to 10 h. The molecular weight also increased to 75,900 g.mol$^{-1}$ over the same period, while the increased monomer concentration resulted in a high molecular weight of 86,400 g.mol$^{-1}$ and a monomer conversion of 84%. Raising the reaction temperature from 90 to 130 $^{\circ}C$ increased the monomer conversion as well as the poly-L-lactide-co-${\varepsilon}$-caprolactone (PLCL) molecular weight. The variation on the stannous octoate catalyst suggested that less catalyst would decrease the caprolactone content of the polymer.

Advancements in Polymer-Filler Derived Ceramics

  • Greil, Peter
    • 한국세라믹학회지
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    • 제49권4호
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    • pp.279-286
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    • 2012
  • Microstructure tailoring of filler loaded preceramic polymer systems offers a high potential for property improvement of Si-based ceramics and composites. Advancements in manufacturing of bulk materials by controlling microstructure evolution during thermal induced polymer-ceramic transforma-tion and polymer-filler reactions will be presented. Rate controlled pyrolysis, multilayer gradient laminate design and surface modification by gas solid reaction are demonstrated to yield ceramic components of high fractional density and superior mechanical properties. Emerging fields of applications are presented.