• Bulletin of the Korean Chemical Society
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• 제18권8호
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• pp.824-827
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• 1997

Bis(ethylene)rhodium(Ⅰ) chloride dimer reacted with vinylcyclopropane to give σ,η3-allylrhodium(Ⅲ) complex 3. Complex 3 underwent C-C bond cleavage of 8-quinolinyl ethyl ketone 11, to form η3-1,3-dimethylallylrhodium(Ⅲ) complex 8, which was reductively eliminated by trimethyl phosphite to give 8-quinolinyl-1-methylbut-2-enyl ketone (10). More sterically hindered 8-quinolinyl alkyl ketones were allowed to react with complex 3 to afford corresponding alkenes as well as a mixture of complex 8 and η3-1-ethylallyl rhodium(Ⅲ) complex 19, identified as 10 and 8-quinolinyl-pent-2-enyl ketone (20) after reductive elimination. 8-Quinolinyl alkyl ketone bearing a sterically hindered alkyl group showed less reactivity for C-C bond cleavage and higher 20/10 ratio compared with those having a less sterically hindered alkyl group, such as 8-quinolinyl ethyl ketone (11).

• Bulletin of the Korean Chemical Society
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• 제21권10호
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• pp.1044-1046
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• 2000

Catalytic copolymerization of diethyl dipropargylmalonate (DEDPM) and phenylacetylene (PA) by Mo(CO)6 and (toluene) Mo(CO)3/chloranil has resulted in the expected copolymer consiting of a polyene backbone with five-and/or six-membered rings and th e PPA structure. Both complexes exhibited not only varying degree of catalytic activity depending upon the relative mole ratio of two monomers but also characterize the types of coploymers. The former yields the polyene backbone containing only five-membered rings as well as PA while the latter produces the polymers consisting of both five-and six-membered ring structure. Comparative studies show that Mo(CO)6 exhibits reactivity toward DEDPM alone, thus catalyzing initially metathesis cyclopoly-merization of DEDPM followed by copolymerization with PA while the (toluene)Mo(CO)3/chloranil system shows affinity for both PA and DEDPM.

• Bulletin of the Korean Chemical Society
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• 제9권3호
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• pp.164-166
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• 1988

7-Dithiocarboxy-3-phenyl-5,6-dihydro imidazo[2,1-b]thiazolium-betaine (2) was prepared by treatment of 3-phenyl-5,6-dihydro imidazo[2,1-b]thiazole (1) with carbon disulfide in acetone at room temperature. On the reaction of 2 with para-substituted phenacyl bromides (4) having the electron withdrawing property by virtue of (+) resonance (R) < (-) inductive (I) or (-) resonance (R), (-) inductive (I) effect, ring transformation product p-substituted-2-[2-[7-(p-substituted benzoyl)-5-thioxo-2,3-dihydro-1H-imidazo[1,2-c] thiazol-1-yl]-2-phenylvinylthio] acetophenone (6) was obtained; however, when R is electron donating grops with (+) resonance (R) > (-) inductive (I) effect the quarternary ammonium salt 7-(p-substituted phenyl) carbonyl methyl-3-phenyl-5,6-dihydro imidazo [2,1-b] thiazolium bromide (8) is formed. The reaction of 2 with unsubstituted-phenacyl bromide (R = H), on the other hand, gives 6a and 8a to the similar ratio, respectively.

• Journal of Korean Society for Atmospheric Environment
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• 제18권E1호
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• pp.29-36
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• 2002

The selective catalytic reduction (SCR) reaction of promoter catalysts was investigated in this study. A pure anatase type of TiO$_2$ was used as support. Activation measurement of prepared catalysts was practiced on a fixed reactor packing by the glass bead after filling up catalysts in 1/4 inch stainless tube. The reaction temperature was measured by K-type thermocouple and catalyst was heated by electric furnace. The standard compositions of the simulated flue gas mixture in this study were as follows: NO 1,780ppm, NH$_3$1,780ppm, $O_2$1% and $N_2$ as balance gas. In this study, gas analyzer was used to measure the outgassing gas. Catalyst bed was handled for 1hr at 45$0^{\circ}C$, and the reactivity of the various catalyst was determined in a wide temperature range. Conversion of NH$_3$/NO ratio and of $O_2$ concentration was practiced at 1,1.5 and 2, respectively. The respective space velocity were as follows . 10,000, 15,000 and 17,000 hr-1. It was found that the maximum conversion temperature range was in a 5$0^{\circ}C$. It was also found toi be very sensitive at space velocity, $O_2$ concentration, and NH$_3$/NO ratio. We also noticed that the maximum conversion temperature of (W, Mo, Sn) -V$_2$O$_{5}$/TiO$_2$ catalysts was broad. Specially WO$_3$-V$_2$O$_{5}$TiO$_2$2 catalyst appeared nearly 100% conversion at not only above 30$0^{\circ}C$ ut also below 25$0^{\circ}C$. At over 30$0^{\circ}C$, NH$_3$ oxidation decreased with decrease of surface excess oxygen. In addition, WO$_3$-V$_2$O$_{5}$TiO$_2$ catalyst did not appear to affect space velocity, $O_2$ concentration, and NH$_3$/NO ratio.ratio.

• 한국수소및신에너지학회논문집
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• 제25권4호
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• pp.344-354
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• 2014

Activated charcoal supported nickel molybdenum carbide (carburized Ni-Mo/AC) catalysts were prepared by wet-impregnation followed by temperature-programmed carburization using 20% $CH_4/H_2$ gas. The effects of pH and initial Ni/Mo mole ratio during wet-impregnation step on the characteristics of the carburized Ni-Mo/AC catalysts were investigated using ICP, XRD, XPS, BET and $CO_2$-TPD techniques, and correlated with the catalytic activity of the carburized Ni-Mo/AC in methane dry reforming reaction. Comparison of the results of methane dry reforming reaction kinetics with the results of characterization of the carburized Ni-Mo/AC catalyst showed that the catalytic activity in methane dry reforming reaction was higher at higher initial Ni/Mo mole ratio or at lower pH(3~natural value). This phenomenon was related to the crystal size of metallic Ni in the carburized Ni-Mo/AC catalyst.

• Korean Chemical Engineering Research
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• 제50권2호
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• pp.217-222
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• 2012

이산화탄소를 이용하여 디메틸카보네이트(DMC)를 제조하는 반응은 지구온난화 현상의 주요 원인으로 지적되는 이산화탄소의 효율적 전환 방법의 하나로 주목 받고 있다. DMC는 유독한 포스겐과 디메틸슬페이트를 대체하는 반응 매개체, 가솔린 연료 첨가제, 폴리카보네이트 수지의 전구체 등으로 다양하게 활용되고 있다. 본 연구에서는 에틸렌카보네이트(EC)와 메탄올의 에스테르 교환반응에 의한 DMC의 제조 반응에 대하여 이온성 액체와 금속 촉매의 특성을 조사하였다. 촉매 스크리닝 실험 결과 [Choline][OH]와 [BMIm][OH]가 금속염인 MgO, ZnO, CaO보다 더 좋은 촉매 활성을 나타내었다. [Choline][OH] 촉매에 대해서 반응변수인 반응온도, MeOH/EC 몰비, 이산화탄소 압력이 반응에 미치는 영향을 고찰하였다. 반응온도가 높고 MeOH/EC 몰비가 클수록 EC의 전화율이 증가하였다. 그러나 이산화탄소 압력의 영향에서는 1.34 MPa에서 최고의 DMC 수율을 나타내었고 그 이상의 압력에서는 DMC 수율이 오히려 감소하였다. $ZnCl_2$를 조촉매로 사용한 경우 각각 촉매의 활성보다 더 높은 활성을 나타내어 시너지 효과가 관찰되었으며, 이것은 혼합촉매의 산-염기적 특성에 기인하는 것으로 판단된다.

• 대한임상검사과학회지
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• 제55권1호
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• pp.45-51
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• 2023

개 파보바이러스(canine parvovirus type 2, CPV-2)와 코로나바이러스(canine coronavirus, CCoV)는 개에서 위장관염을 일으키는 주요 병원체이다. 두 바이러스는 전염성과 이환율이 높고 특정한 치료법이 없어 신속 정확한 진단이 필요하다. 동물용 신속진단키트 (rapid diagnostic test, RDT)는 빠르고, 간편하여 진료현장에서 널리 활용되고 있다. 이에 본 연구에서는 성능평가를 통해 CPV-2/CCoV RDT의 임상적 유용성을 확인하고자 하였다. 성능평가 항목으로 최소검출한계(limit of detection, LoD), 교차반응, 간섭, 민감도, 특이도, 음성우도비(negative likelihood ratio, NLR), 카파통계량(kappa value, κ) 등을 확인하였다. 성능평가 결과, LoD는 CPV-2 9.7×10 50% tissue culture infections dose (TCID₅₀)/mL, CCoV 2.5×10² TCID₅₀/mL로 나타났다. 병원체 9종에 의한 교차반응과 간섭물질에 대한 간섭은 관찰되지 않았다. RDT는 두 바이러스의 검출에 있어 민감도 90.0%, 특이도 100.0%, NLR=0.1, κ=0.90으로 나타났다. 결론적으로 CPV-2/CCoV RDT는 높은 민감도, 특이도, κ와 낮은 NLR을 보여 선별검사로써 유용할 것으로 생각된다.

• Bulletin of the Korean Chemical Society
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• 제31권9호
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• pp.2593-2597
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• 2010

Second-order rate constants ($k_N$) have been measured spectrophotometrically for reactions of 2,4-dinitrophenyl X-substituted benzoates (X = 4-MeO, H and 4-$NO_2$) with a series of Z-substituted pyridines in 80 mol % $H_2O$/20 mol % DMSO at $25.0{\pm}0.1^{\circ}C$. The Br${\o}$nsted-type plots exhibit downward curvature (e.g., $\beta_2$ = 0.89 ~ 0.96 when $pK_a$ < 9.5 while $\beta_1$ = 0.38 ~ 0.46 when $pK_a$ > 9.5), indicating that the reaction proceeds through a stepwise mechanism with a change in rate-determining step (RDS). The ${pK_a}^o$, defined as the $pK_a$ at the center of Br${\o}$nsted curvature, has been analyzed to be 9.5 regardless of the electronic nature of the substituent X in the benzoyl moiety. Dissection of $k_N$ into the microscopic rate constants $k_1$ and $k_2/k_{-1}$ ratio has revealed that $k_1$ is governed by the electronic nature of the substituent X but the $k_2/k_{-1}$ ratio is not. Theoretical calculations also support the argument that the electronic nature of the substituent X in the benzoyl moiety does not influence the $k_2/k_{-1}$ ratio.

• 자원리싸이클링
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• 제30권1호
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• pp.83-91
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• 2021

조강 생산 시 발생되는 슬래그는 대부분 서냉 방식에 의해 처리되고 있다. 하지만 슬래그 중 일부는 속경성 광물을 포함하고 있음에도 불구하고, 서냉 방식에 의해 그 반응성을 상실하게 된다. 이에 본 연구에서는 제강환원슬래그를 SAT공법에 의하여 공기 급냉하여 선별 및 분급 후 분쇄한 CAC의 활용성 확대를 목적으로 석고 종류 및 혼입율에 따른 CAC의 특성에 관하여 고찰하였다. 그 결과, CAC는 3시간에서는 석고 용해도, 1일 이후에는 석고 함량비에 따라 특성이 나타나는 것을 확인하였다. 반수, 무수석고의 적정 혼입율은 30% 이내, 이수석고는 35% 이상인 것을 확인하였으며, 이수석고의 혼입율 및 특성 확인을 통하여 부산이수석고의 적용 가능성을 확인하였다.

• 공업화학
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• 제18권2호
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• pp.155-161
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• 2007

본 연구에서는 $SnO_2-ZrO_2$(Sn/Zr = 2/1) 촉매 상에서의 CO에 의한 $SO_2$ 환원반응에 대한 반응온도, 공간속도, [CO]/[$SO_2$] 몰비 등의 반응조건의 최적화를 위한 반응특성을 조사하였다. $300{\sim}550^{\circ}C$의 반응온도, $5000{\sim}30000cm^3/g_{-cat}{\cdot}h$의 공간속도, 1.0~4.0 의 [CO]/[$SO_2$] 몰비 등 다양한 반응조건 범위에서 CO에 의한 $SO_2$ 환원반응에 대한 영향을 살펴본 결과, 최적 반응조건으로 반응온도, 공간속도, [CO]/[$SO_2$] 몰비는 각각 $325^{\circ}C$, $10000cm^3/[g_{-cat}{\cdot}h]$, 2.0이었다. 이 때 $SO_2$ 전환율은 약 99% 이상이었으며, 원소 황 선택도는 95% 이상이었다. 또한 CO에 의한 $SO_2$ 환원반응에서 수분에 대한 영향을 조사한 결과, 수분함량이 2.0~6.0 vol%인 범위에서 수분의 함량이 높을수록 $SO_2$ 전환율 및 원소 황 선택도가 감소됨과 동시에 반응성이 저하됨을 알 수 있었다. 2 vol%의 수분이 함유된 반응조건에서 반응온도와 [CO]/[$SO_2$] 몰비를 각각 $300{\sim}400^{\circ}C$ 및 1.0~3.0으로 변화시킨 결과, 반응온도와 [CO]/[$SO_2$] 몰비가 각각 $340^{\circ}C$와 2.0인 조건에서 가장 높은 반응성을 얻었다. 이 때 $SO_2$ 전환율이 약 90%였으며, 원소 황 선택도는 약 87%였다