• Bulletin of the Korean Chemical Society
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• 제8권6호
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• pp.466-470
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• 1987

Di-2-pyridyl thionocarbonate, prepared from thiophosgene and 2-hydroxypyridine in the presence of triethylamine in dichloromethane, was found to be very effective for dehydration, dehydrosulfurization, and thiocarbonyl transfer reactions. Di-2-pyridyl thionocarbonate was successfully for the esterification of carboxylic acids, dehydration of aldoximes into nitriles, preparation of isothiocyanates from amines, and preparation of cyclic thionocarbonates from 1,2- and 1,3-diols.

• 한국진공학회:학술대회논문집
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• 한국진공학회 2012년도 제42회 동계 정기 학술대회 초록집
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• pp.284-284
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• 2012

In this study, $V_2O_5/TiO_2$ catalyst was measured reactivity of ethanol when vanadia ratio was increasing. First, $V_2O_5/TiO_2$ catalyst was prepared to the increasing vanadia ($VO_x$) ratio as 0.2, 1, 10 wt%. And we were used X-ray diffraction (XRD), then not appear markedly peak to pure vanadia about XRD analysis. So we were decided vanadia that was evenly dispersed on $TiO_2$. Result about temperature-programmed reduction (TPR) analysis was obtained 3 reactions that was dehydrogenationfrom obtained to acetaldehyde, dehydration from obtained to ethylene, condensation from obtained to diethyl ether. If vanadia ratio was increasing in $V_2O_5/TiO_2$, reactions temperature of ethanol was known lower. And condensation into diethyl ether is quenched away with increasing vanadia loading. In addition, competition between reductive dehydration and oxidative dehydrogenation occurs, while the selectivity toward dehydrogenation is favored with increasing vanadia loading.

• 한국건축시공학회:학술대회논문집
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• 한국건축시공학회 2013년도 추계 학술논문 발표대회
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• pp.154-155
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• 2013

The aim of this work is to have a better knowledge of reactions that take place in a cement paste, blast furnace slag mixed cement paste and fly ash mixed cement paste and know about the change in chemical components exposed to elevated temperature. The results show that the dehydration reactions appeared differently in the each admixture mixed cement paste and can be used as tracers for determining the temperature history of concrete after a fire exposure.

• Bulletin of the Korean Chemical Society
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• 제26권4호
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• pp.609-613
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• 2005

The fragmentation patterns and ion-molecule reactions of two alkyn alcohols, 2-propyn-1-ol (HC≡$CCH_2$OH) and 2-methyl-3-butyn-2-ol (HC≡CC($CH_3)_2$OH), were investigated using Fourier transform mass spectrometry (FTMS). The most abundant fragment ions formed from the molecular ions were [M-H]$^+$ for 2-propyn-1-ol and [M-$CH_3]^+$ for 2-methyl-3-butyn-2-ol. The dehydrated ion, [M-$H_2O]^+$ was formed only from 2-propyn-1-ol in which $\alpha$ -hydrogen atoms were available for $\alpha,\;\alpha$ -elimination reaction. The protonated molecules were dissociated into [M+H-$H_2O]^+$ and [M+H-$C_2H_2]^+$ through dehydration and deacetylenylation processes. The formations of [M+H-$H_2O]^+$ and [M+H-$C_2H_2]^+$ from 2-methyl-3-butyn-2-ol were more favorable than those from 2-propyn-1-ol due to stabilization by two methyl groups at $\alpha$ -carbon. Ion-neutral complexes formed at long ion trapping time gave dehydrated and/or deacetylenylated ion products by further dissociation.

• Current Research on Agriculture and Life Sciences
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• 제7권
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• pp.175-184
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• 1989

대표적인 재료로서 바나나를 선정하여 건조방법과 조건에 따른 최적화에 사용할 수 있는 Ascorbic acid 저하속도와 비효소적 갈변속도에 대한 반응속도 예측 모델식을 결정하였다. Ascorbic acid 저하 속도와 비 효소적 갈변속도를 각각 1차반응, 0차반응으로, 두반응의 온도 의존성은 Arrhenius식으로 나타내어 SPSS Computer Program을 이용하여 실제 측정된 Ascorbic acid와 비효소적 갈변의 data에 가장 접근하도록 Parameter를 반복계산하여 찾았다. 얻어진 반응속도식에서의 Parameter값들은 R. SQUARE값이 평균 0.99이상이므로 살험치를 잘 예측하였으며 건조공정의 최적화에 이용될 수 있을 것으로 생각되어진다. Ascorbic acid 저하속도와 비효소적 갈변속도는 건조초기에 낮고 건조가 진행되어 수분함량의 감소와 함께 최대속도를 보이다가 서서히 감소하였다. 이때 동결건조의 경우가 가장 안정된 품질변화를 나타냈음을 알 수 있었다.

• Bulletin of the Korean Chemical Society
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• 제25권10호
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• pp.1538-1544
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• 2004

Fragmentations and proton transfer reactions of mono-, di-, and triethanolamines were studied using FTMS. It was found that the most abundant fragment ion was $[M-CH_2OH]^+$. The $[M-CH_2OH-H_2O]^+$ was observed in the mass spectra of diethanolamine and triethanolamine. By increasing the ion trapping time in the ICR cell, the $[M+H]^+$ and $[M+H-H_2O]^+$ ions were notably increased for all the samples while the $[M+H-2H_2O]^+$ was observed in the mass spectra of diethanolamine and triethanolamine. The proton transfer reactions between the fragment ions and neutral molecules occurred predominantly by increasing the ion trapping time. The rate constants for the proton transfer reactions were calculated from experimental results. The proton transfer reaction of $CHO^+$ was the fastest one, which is consistent with the heats of reaction. The rate constants for proton transfer reactions of triethanolamine were much slower than those of ethanolamine and diethanolamine because of the steric hindered structure of triethanolamine. The plausible structures of observed ions and heats of reaction for proton transfer were calculated with AM1 semiempirical method.

• Bulletin of the Korean Chemical Society
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• 제22권12호
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• pp.1309-1315
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• 2001

Zirconium sulfate supported on zirconia catalysts were prepared by impregnation of powdered $Zr(OH)_4$ with zirconium sulfate aqueous solution followed by calcining in air at high temperature. The characterization of prepared catalysts was performed using Fourier transform infrared (FTIR), X-ray diffraction (XRD), differential scanning calorimetry (DSC), and by the measurement of surface area. The addition of zirconium sulfate to zirconia increased the phase transition temperature of $ZrO_2$ from amorphous to tetragonal due to the interaction between zirconium sulfate and zirconia, and the specific surface area and acidity of catalysts increased in proportion to the zirconium sulfate content up to 10 wt% of $Zr(SO_4)_2$. Infrared spectra of ammonia adsorbed on $Zr(SO_4)2}ZrO_2$ showed the presence of Bronsted and Lewis acid sites on the surface. $10-Zr(SO_4)_2}ZrO_2$ calcined at $600^{\circ}C$ exhibited maximum catalytic activities for 2-propanol dehydration and cumene dealkylation. The catalytic activities for both reactions were correlated with the acidity of catalysts measured by ammonia chemisorption method.

• Bulletin of the Korean Chemical Society
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• 제11권5호
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• pp.403-406
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• 1990

Two types of new silica catalysts modified with benzenesulfonic acid derivatives were prepared by esterification or phenylation followed by sulfonation. Both catalysts thus prepared were tested as acid catalysts for 2-propanol dehydration and cumene dealkylation reactions. B catalyst () were more active than A catalyst (). Highter catalytic activity for B catalyst may be accounted for by higher resistance to water, higher acid strength, more acidity, and better thermal stability as compared with A catalyst.

• 멤브레인
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• 제33권6호
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• pp.305-314
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• 2023

화학 반응의 수율 향상을 위해 부산물을 제거하는 다양한 방법이 연구되고 있다. 특히 산업적으로 중요한 반응에서 주로 부산물로 물이 생성되기 때문에 넓은 범위의 온도에서 안정적으로 물을 분리하는 기술이 필요하다. 흡수제의 사용, 탈수 반응의 도입 등 다양한 방법이 제안되었으나 추가적인 에너지 및 시간 소요, 전환율의 지속 가능성 등의 문제로 한계를 가지고 있다. 그에 반해 운전 및 설치가 용이하고, 낮은 유지비용 등의 장점을 가지고 있는 분리막 기술은 다양한 촉매 반응에 도입되었을 때 안정적으로 부산물을 제거할 수 있어 반응의 효율을 향상시킬 수 있는 좋은 방안이다. 따라서 본 총설에서는 분리막을 이용한 부산물 제거 및 이를 통한 효과에 대해 논의하였다.

• Bulletin of the Korean Chemical Society
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• 제25권5호
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• pp.657-664
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• 2004

Titanium sulfate supported on $TiO_2$was prepared by impregnation of powdered $TiO_2$with an aqueous solution of titanium sulfate followed by calcining in air at high temperature. For Ti$(SO_4)_2/TiO_2$ samples calcined at 300 $^{\circ}C$, no diffraction lines of titanium sulfate are observed at $Ti(SO_4)_2$loading up to 30 wt%, indicating good dispersion of $Ti(SO_4)_2$ on the surface of $TiO_2$. The acidity of the catalysts increased in proportion to the titanium sulfate content up to 20 wt% of $Ti(SO_4)_2$. 20 wt% $Ti(SO_4)_2/TiO_2$ calcined at 300 $^{\circ}C$ exhibited maximum catalytic activities for 2-propanol dehydration and cumene dealkylation. The catalytic activities for these reactions, were correlated with the acidity of catalysts measured by ammonia chemisorption method.