• Bulletin of the Korean Chemical Society
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• 제18권8호
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• pp.806-810
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• 1997

A series of new hydridocarbonyl osmium(Ⅱ) complexes, OsHCl(CO)(PPh3)(L-L)[L-L=Ph2P(CH2)nPPh2 (n=1 (1), 2 (2), 3 (3), cis-Ph2PCH=CHPPh2 (4), and Fe(η5-C5H4PPh2)2 (5)] has been synthesized from OsHCl(CO)(PPh3)3 and chelating diphosphines. These complexes have been characterized by IR, 1H NMR and elemental analysis. The catalytic activities of these complexes both for the transfer hydrogenation of trans-cinnamaldehyde with 2-propanol as the hydrogen donor, and for the selective hydrogenation of trans-cinnamaldehyde with H2, have been examined. Complexes (1)-(5) were shown to have higher selectivities for the transfer hydrogenation of the C=O bond of aldehyde than for the transfer hydrogenation of the C=C bond of aldehyde. The selectivities for the transfer hydrogenation with 2-propanol as well as for the hydrogenation with H2 have been found to decrease in the order 3 > 5 > 2 > 4 > 1. Complex (3) has shown to possess almost 90% of the selectivity to cinnamyl alcohol for transfer hydrogenation. It is also found that there is a correlation between the ν(CO) of each complex and the hydrogenation, of the C=O bond of trans-cinnamaldehyde. Overall, the selectivities with the complexes (1)-(5) are greater for the transfer hydrogenation with 2-propanol than for the hydrogenation with H2.

• Bulletin of the Korean Chemical Society
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• 제30권6호
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• pp.1317-1324
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• 2009

Asymmetric transfer hydrogenation of α-functionalized arylketones has been studied. The chiral Rh-catalyst effectively performed in transfer hydrogenation of $\alpha$-mesyloxyketones with an azeotropic mixture of formic acid/triethylamine to produce optically active 1-arylethandiols with excellent enantioselectivity.

• Bulletin of the Korean Chemical Society
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• 제30권9호
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• pp.1931-1932
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• 2009

• Bulletin of the Korean Chemical Society
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• 제24권9호
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• pp.1407-1409
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• 2003

• Journal of Industrial and Engineering Chemistry
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• 제67권
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• pp.486-496
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• 2018

Bimetallic Pd@Ni nanostructure exhibited enhanced co-catalytic activity for the selective hydrogenation of benzaldehyde compare to their monometallic counterparts. Impregnation of these mono/bimetallic nanostructures on mesoporous $TiO_2$ leads to several surface modifications. The bimetallic PNT-3 ($Pd_3@Ni_1/mTiO_2$) exhibited large surface area ($212m^2g^{-1}$), and low recombination rate of the charge carriers ($e^--h^+$). The hydrogenation reaction was analyzed under controlled experiments. It was observed that under UV-light irradiations and saturated hydrogen atmosphere the bimetallic PNT-3 photocatalyst display higher rate constant $k=5.31{\times}10^{-1}h^{-1}$ owing to reduction in the barrier height which leads to efficiently transfer of electron at bimetallic/$mTiO_2$ interface.

• Bulletin of the Korean Chemical Society
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• 제34권10호
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• pp.3143-3146
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• 2013

• 공업화학
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• 제10권8호
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• pp.1210-1215
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• 1999

Pd/C촉매가 부유되어 있는 3상 슬러리 반응기에서 원료 p-nitroaniline(PNA)를 수소 첨가시켜 고순도의 p-phenylenediamine(PPD)를 합성하는 최적 반응조건을 구하였다. 수소첨가 반응시 활성점에서 수소부족을 줄이고 불순물의 생성을 감소시킬 수 있도록, 기체-액체, 액체-촉매사이의 물질전달 저항을 최소화하고 표면반응속도가 율속할 수 있게 반응조건을 설정하였다. 이 반응조건은 온도 $60^{\circ}C$, 압력 60~70 psig, 촉매농도 1~2 g-cat/L일 때가 최적이었으며, 반응속도는 PNA 농도에 0차, 수소 반응압력에 1차를 각각 보여주었으며, 총괄반응속도식은 $R_A=6.44{\times}10^6{\cdot}H{\cdot}P{\cdot}m{\cdot}$exp(-4659/T)로 나타났다.

• 공업화학
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• 제24권6호
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• pp.650-655
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• 2013

본 연구에서는 Pd/C 촉매를 이용하여 무수말레인산(maleic anhydride) 수용액상에서 수소화 반응을 통해 호박산(succinic acid) 합성을 진행하였으며, 그에 따른 최적 공정 조건을 도출하고자 하였다. 반응 온도 및 반응시간에 따른 호박산 순도의 차이는 크지 않았으나 압력과 교반속도가 증가함에 따라 불순물의 생성이 줄고, 호박산의 순도가 증가함을 확인하였다. 실험 결과 본 수소화 반응에서는 압력과 교반속도가 기체-액체 간 물질전달저항을 감소시켜 반응속도를 증가시킬 수 있는 가장 중요한 변수임을 확인하였으며 이에 따라 압력과 교반속도에 대한 반응속도를 구하였다. 반응압력이 5 bar에서 10 bar로 2배 증가 시, 반응속도는 2.14배 증가하였으며 교반속도가 300 rpm에서 700 rpm으로 2배 증가 시, 반응속도는 2.36배 증가함을 확인할 수 있었다.

• 한국수소및신에너지학회논문집
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• 제8권1호
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• pp.31-41
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• 1997

In order to investigate the mechanism of electrochemical hydrogenation reaction on Zr-based Laves phase hydrogen storage alloy electrodes, electrochemical charge/discharge characteristics, potentiostatic/dynamic polarizations and electrocehmical impedance spectroscopy(EIS) of Zr-Ti-Mn-Ni and Zr-Ti-Mn-Ni-M(M=Fe, Co, Al) alloys were examined. Electrochemical discharge capacities of the alloys were quite different with gas charge capacities. Therefore, it was considered that discharge capacities of the alloys depend on electrochemical kinetic factors rather then thermodynamic ones. Discharge efficiencies were increased linearly with exchange current densities. The results of potentiostatic/dynamic polarization measurements showed that electrochemical charge and discharge reaction of Zr-based Laves phase hydrogen storage alloys is controlled by charge transfer process at the electrode surface. The EIS measurements also confirmed this result.

• 한국수소및신에너지학회논문집
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• 제34권6호
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• pp.608-614
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• 2023

The fast filling process of high-pressure hydrogen has an important impact on the filling efficiency and safety. In this paper, a specific study is carried out on the thermophysical phenomena during the fast filling process. Starting from the gas state equation of hydrogen, the change law of the hydrogen storage temperature is obtained, and then the temperature rise prediction is constructed. The model can clarify the relationship between the filling parameters and the temperature rise during the fast filling process, thereby revealing the flow and heat transfer laws of the fast charging process. To improve the theoretical research basis for the evaluation of vehicle-mounted hydrogen fast charging capacity, temperature prediction and optimization of hydrogenation methods.