• 제목/요약/키워드: chemical reactivity

검색결과 813건 처리시간 0.029초

백운석의 소성 조건에 따른 제조 Mg crown의 특성에 관한 연구 (A Study on the Characteristics of Manufactured Mg Crown on the Calcining Conditions of Dolomite)

  • 황대주;유영환;이종대
    • Korean Chemical Engineering Research
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    • 제59권4호
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    • pp.611-625
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    • 2021
  • 국내에서 채광한 백운석(Ca·Mg(CO3)2) (20~30 mm)을 활용하여 Mg crown을 제조하였다. 백운석을 사용하여 경소 백운석(CaO·MgO)을 제조하기 위하여, (a) 전기로(950 ℃, 480분)와 (b) 마이크로웨이브 가열로(950 ℃, 60분)를 사용하는 공정을 적용한 결과를 서로 비교하였다. 전기로 공정의 경우에는 CaO 56.9 wt%, MgO 43.1 wt%, 마이크로웨이브 가열로 공정의 경우에는 CaO 55 wt%, MgO 45 wt%가 얻어졌다. 마이크로웨이브 가열로를 사용한 공정에서는 백운석의 탈탄산 반응 시간을 1/8로 단축하여도 경소백운석을 제조할 수 있었다. 수화 시험(hydration reaction, ASTM C110)은 경소백운석의 수화 반응성의 기준이 되는데, 전기로 공정의 경우에는 고 반응성(최고 온도 79.8 ℃/1.5 분)을 나타내었다. 이러한 수화 반응은 CaO의 수화 반응에 의해 일어나는 것을 XRD 분석 결과에서 확인할 수 있었으며, 마이크로 가열로 공정의 경우에는 저 반응성(최고 온도 81.7 ℃/19.5 분)을 나타내었다. 이러한 낮은 수화 반응성은 CaO의 수화 반응이 일어난 후에 MgO의 수화 반응이 일어나서 CaO와 MgO가 모두 수화물 형태로 되는 것을 XRD 분석 결과에서 확인하였다. 전기로와 마이크로웨이브 가열로를 사용하여 1,230 ℃, 60분, 5 × 10-2 torr의 조건에서 규소열환원 공정으로 제조한 Mg crown은 전기로 공정의 경우에 58.8 g 그리고 마이크로웨이브 가열로 공정의 경우에 74.6 g을 얻을 수 있었다.

Copolymerizations of Ethylene with 1-Hexene over ansa-Metallocene Diamide Complexes

  • Kim, Il;Kwak, Chang-Hun;Son, Gi-Wan;Kim, Jae-Sung;Sinoj Abraham;Bijal K. B.;Ha, Chang-Sik;Kim, Bu-Ung;Jo, Nam-Ju
    • Macromolecular Research
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    • 제12권3호
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    • pp.316-321
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    • 2004
  • We have performed copolymerizations of ethylene with 1-hexene using various ansa-metallocene compounds in the presence of the non-coordinative [CPh$_3$][B(C$\_$6/F$\_$5/)$_4$ion pair as a cocatalyst. The metallocenes chosen for this study are isospecific metallocene diamide compounds, rac-(EBI)Zr(NMe$_2$)$_2$ [1, EBI = ethylene-l ,2-bis(1-indenyl)], rac-(EBI)Hf(NMe$_2$)$_2$ (2), rac-(EBI)Zr(NC$_4$H$\_$8/)$_2$ (3), and rac-(CH$_3$)$_3$Si(1-C$\_$5/H$_2$-2-CH$_3$-4-$\^$t/C$_4$H$\_$9/)2 Zr(NMe$_2$)$_2$ (4), and syndiospecific metallocene dimethyl compounds, ethylidene(cyclopentadienyl)(9-fluorenyl) ZrMe$_2$ [5, Et(Flu)(Cp )ZrMe$_2$] and isopropylidence (cyclopentadienyl)(9-fluorenyl)ZrMe$_2$ [6, iPr(Flu)(Cp)ZrMe$_2$]. The copolymerization rate decreased in the order 4 >1-3>2 >5>6. The reactivity of I -hexene decreased in the order 2 >6>1- 3-5> 4. We characterized the microstructure of the resulting poly(ethylene-co-l-hexene) by $\^$l3/C NMR spectroscopy and investigated various other properties of the copolymers in detail.

암모니아로부터 수소 제조를 위한 다양한 촉매 활성 테스트에 관한 연구 (A Study on Activity Testing of Various Catalysts for Hydrogen Production from Ammonia)

  • 이재혁;신경하;강진실;신현희;박세연;최유진;송완규;안호근
    • 한국수소및신에너지학회논문집
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    • 제34권6호
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    • pp.587-593
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    • 2023
  • This research project focused on the production of hydrogen through ammonia decomposition reactions while investigating how the reactivity of this process varies when employing different catalysts. Several metal oxide supports (Al2O3, La2O3, CeO2) were utilized as catalysts, with active metals from both the transition metal group (Co, Ni, Fe, Cr, Cu) and the noble metal group (Ru, Rh, Pd, Pt) impregnated onto these supports. Furthermore, the study examined how the reactivity evolves with changes in reaction temperature when employing the prepared catalysts. Additionally, the research delved into the distinctive activation energies associated with each of the catalysts. In this research, In the noble metal catalyst system, the order of high activity for ammonia decomposition reaction to produce hydrogen is Ru > Rh > Pt ≈ Pd. In the transition metal catalyst system, the order of high activity is Co > Ni > Fe > Cr > Cu.

H2S제거를 위한 아연계 탈황제 제조 및 반응특성 연구 (A Study on Preparation and Reactivity of Zinc-based Sorbents for H2S Removal)

  • 이창민;윤여일;김성현
    • 공업화학
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    • 제10권2호
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    • pp.183-189
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    • 1999
  • $H_2S$를 제거를 위한 아연계 복합금속산화물 탈황제를 제조하고 반응특성을 연구하였다. 최적 황화반응 온도인 $650^{\circ}C$의 고정층에서 탈황-재생의 연속 cycle에 따른 반응성을 관찰하였다. 내마모성 향상을 위한 구형입자의 탈황제를 제조하기 위해 Granulation방법을 이용하였다. XRD와 XPS분석에 의해 zinc titanate결정생성을 확인하였고 소성조건에 따른 탈황제의 특성을 분석하기 위해 mercury porosimetry와 BET분석을 행하였다. Cycle이 증가함에 따라 고온에서의 zinc loss와 sintering, cracking, 그리고 spalling에 의한 탈황제의 확산저항의 증가로 인해 반응성은 떨어졌다.

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$BaCeO_3$계 프로톤 전도 산화물의 화학적 불안정성 (Chemical Instability of $BaCeO_3$-Based Proton Conducting Oxide)

  • 변명섭;강은태;조우석;김진호;황광택
    • 한국수소및신에너지학회논문집
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    • 제22권1호
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    • pp.92-99
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    • 2011
  • Barium cerate ($BaCeO_3$) related perovskite ceramics currently dominate the high-temperature proton conductor field. Unfortunately, these materials have very stringent environmental limitations necessitating the costly and complex conditioning or cleaning of the application feed-gas. Commercial realization has been hampered, in part, because of the reactivity of $BaCeO_3$ with $CO_2$, and to some extent $H_2O$. And sintered $BaCeO_3$ decomposed at a rate comparable to the powder samples. In this article, the chemical stability and the structural changes of $BaCe_{0.9-X}Y0.1La_XO_{3-\delta}$ (X=0, 0.1, 0.2) have been systematically investigated in the atmosphere containing carbon dioxide ($CO_2$) and water vapor ($H_2O$). The sintering characteristics were studied in $1600^{\circ}C$, sintered pellets disintegrate and decompose upon contacting boiling water on the surface only.

0.5 MWth 케미컬루핑 연소 시스템 적용을 위한 신규 산소전달입자의 고온·고압 반응 특성 (Reaction Characteristics of New Oxygen Carrier for 0.5 MWth Chemical Looping Combustion System at High Temperature and High Pressure Conditions)

  • 김정환;이도연;남형석;조성호;황병욱;백점인;류호정
    • 한국수소및신에너지학회논문집
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    • 제29권5호
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    • pp.473-482
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    • 2018
  • To check applicability of recently developed new oxygen carrier for 0.5 MWth chemical looping combustion system, reactivity tests were carried out at high temperature and high pressure conditions. Pressure, temperature, gas velocity, $CH_4$ flow rate, and solid height were considered as operating variables. The new oxygen carrier (N016-R4) showed not only high fuel conversion but also high $CO_2$ selectivity within all the operating conditions in this study. The reactivity of N016-R4 particle was compared with previous oxygen carriers. The N016-R4 particle represented outstanding reactivity among 10 oxygen carriers in terms of fuel conversion and $CO_2$ selectivity.

Effects of Reaction pH and Hardener Type on Reactivity, Properties, and Performance of Urea-Formaldehyde (UF) Resin

  • Park, Byung-Dae;Kim, Yoon Soo;So, Won Tek;Lim, Kie Pyo
    • Journal of the Korean Wood Science and Technology
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    • 제30권3호
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    • pp.1-11
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    • 2002
  • This study was conducted to investigate the effects of reaction pH conditions and hardener types on the reactivity, chemical structure and adhesion performance of UF resins. Three different reaction pH conditions, such as traditional alkaline-acid (7.5 → 4.5), weak acid (4.5), and strong acid (1.0), were used to synthesize UF resins which were cured by adding three different hardeners (ammonium chloride, ammonium citrate, and zinc nitrate) to measure adhesion strength. Fourier transform infrared (FT-IR) and carbon-13 nuclear magnetic resonance (13C-NMR) spectroscopies were employed to study chemical structure of the resin prepared under three different reaction pH conditions. Adhesion strength of the resins cured with three different hardeners was determined with lap shear specimens in tension. The gel time of UF resins decreased with an increasing in the amount of both ammonium chloride and ammonium citrate added in the resins. However, the gel time increased for zinc nitrate. Both FT-IR and 13C-NMR spectroscopies showed that the strong reaction pH condition produce uronic structures in UF resin, while both alkaline-acid and weak acid conditions produce quite similar chemical species in the resins. The maximum adhesion strength was occurred with the resin prepared under strong acid pH condition. However, this study indicated that the weak acid reaction condition provide a balance between increasing resin reactivity and improving adhesion strength of UF resin. The measurement of formaldehyde emission from the panels bonded with the UF resins prepared is planned for future work.

Copolymerization of Glycidyl Methacrylate with Methyl Acrylate

  • Suck-Ju Hong
    • 대한화학회지
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    • 제15권5호
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    • pp.281-284
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    • 1971
  • Copolymerization of glycidyl methacrylate(GMA) with methyl acrylate(MA) and the reaction of the copoly mer with primary amines were investigated. The monomer reactivity ratios were determined by Mayo-Lewis intersecting method. $r_1=0.22{\pm}0.03(GMA),\;r_2=0.50{\pm}0.07(MA)$. GMA and MA copolymerized to afford the polymer having good alternate arrangements of the units of the monomers.

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