• Bulletin of the Korean Chemical Society
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• 제16권6호
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• pp.528-533
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• 1995

Metallic iridium and rhodium powders prepared from the reactions of [M(COD)(PhCN)2]ClO4 (M=Ir(1), Rh(2); COD=1,5-cyclooctadiene) with hydrogen at room temperature in methylene chloride show catalytic activities for hydrogenation of arenes at room temperature under atmospheric pressure of hydrogen. Most substituents (CH3, COOH, NO2, CH2OH, CHO, OPh, OCH3, C=C, halogens and CH2Cl) on aromatic ring suppress the rate of the hydrogenation of the aromatic ring while the aromatic ring hydrogenation of phenol and 1,4-dihydroxobenzene is faster than that of benzene over these metallic powders. Hydrogenation of benzoic acid occurs only at the aromatic ring leaving the COOH group intact over iridium metal powders while benzoic acid is not hydrogenated at all over rhodium metal powders. Carbonyl, nitro, acetylenic and olefinic groups on an aromatic ring are hydrogenated prior to the aromatic ring hydrogenation. Hydrogenolysis of OH groups of phenol, benzyl alcohol and 1,4-dihydroxobenzene, and hydrodehalogenation of halobenzenes, benzyl halides and cinnamyl chloride also occur along with the hydrogenation of aromatic ring.

• 한국대기환경학회지
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• 제15권2호
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• pp.183-190
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• 1999

Magnetite was synthesized with $FeSO_4$, and NaOH for the decomposition of carbon dioxide and for the study of the methane formation. The chemical equivalent ratio was changed from 0.5 to 1.50 for the magnetite synthesis. The chemical equivalent ratio was fixed in 1.00, and Nickel chloride and Rhodium chloride equally added and synthesized with the ratio was of 0.10~10.00 mole%. The crystal strucure of the synthesized magnetite was measured XRD. Putting synthesized magnetite in the reactor and using hydrogen gas oxygen-deficient magnetite was made. Injecting carbon dioxide in the reactor, the decomposition reaction was experimented. The formation of methane was confirmed injecting hydrogen gas in the reactor after carbon dioxide was decomposed.

• 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).

• 자원리싸이클링
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• 제22권5호
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• pp.29-34
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• 2013

TEHA와TEHA 및TBP와 LIX63과의 혼합용매를 사용하여 염산용액으로부터 백금과 로듐을 분리하기 위한 용맥추출실험을 수행하였다. 염산농도 1-9 M 범위에서 추출제의 농도에 따른 두 금속의 추출거동과 분리 가능성을 조사하였다. 혼합용액에서 백금과 로듐의 농도는 각각 $1{\times}10^{-3}M$과 $2{\times}10^{-4}M$로 조절하였다. TEHA와 혼합추출제에 의한 추출시 로듐의 추출율은 추출조건에 의존하나, 백금은 염산농도와 무관하게 모두 추출되었다. 혼합용액에서 염산농도가 낮을 경우 로듐이 추출되지 않아 백금과 로듐의 분리가 가능하였다. LIX63을 첨가한 TEHA는 로듐의 추출율을 향상시켰으나, TBP를 첨가한 TEHA는 두 금속의 추출에 거의 영향을 미치지 않았다.

• Bulletin of the Korean Chemical Society
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• 제31권7호
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• pp.1945-1950
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• 2010

Solvent extraction experiments of Pt(IV), Pd(II) and Rh(III) by Alamine336 were performed from the mixed chloride solutions. In the HCl concentration range from 1 to 5 M, most of Pt and Pd were extracted from the mixed solutions. However, the extraction percentage of Rh was much smaller than that of Pt and Pd. Lower concentration of Alamine336 in strong HCl solution led to higher separation factor of Rh from Pt and Pd. Adding $SnCl_2$ to the mixed solutions increased the extraction percentage of Rh, while the extraction percentage of Pt and Pd was little affected. Our results showed that selective separation of Rh or coextraction of the three platinum group metals from the mixed solution would be possible by adjusting the extraction conditions.

• 한국가스학회지
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• 제2권2호
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• pp.40-47
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• 1998

이산화탄소를 분해할 목적으로 황산철과 수산화나트륨을 이용하여 $Fe_3O_4$를 합성하였다. 합성조건은 황산철과 수산화나트륨의 혼합당량비를 0.50${\~}$l.50까지로 반응온도는 $40^{\circ}C$, 반응시간은 20시간으로 하였다. 또한 혼합당량비를 1.00으로 고정하고, 여기에 $NiCl_2,\;RhCl_3$를 mole$\%$로 첨가하여 합성하였다. 이 합성된 $Fe_3O_4$의 구조변화에 미치는 Ni과 Rh의 영향을 XRD, SEM으로 비교 검토하였다.

• 자원리싸이클링
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• 제27권3호
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• pp.93-99
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• 2018

본 연구에서는 디스플레이 산업의 백금 폐스크랩을 용해, 용매추출을 통하여 백금족 성분을 효율적으로 추출하고, 추출된 백금용액을 디젤자동차 배가스 정화촉매용 전구체 용액으로서 제조하고, 그 촉매활성을 실험하였다. 용액화학적 이론 연구를 통하여 백금 화학종의 수용액상 거동을 조사하였고, 화학종들의 존재영역 및 거동을 근거로 추출 및 분리 가능방안을 수립하였다. 전기화학적 방법에 의해 폐스크랩을 용해시킴으로써, 용해시간 단축 및 추출효율을 높였으며, 로듐 성분을 분리 제거, TBP에 의한 용매추출, 염산에 의한 탈거 공정을 거쳐 Pt-Chloride-$H_2O$ 계 백금용액을 용액을 제조하고, 이 용액을 원료로 액상 아민화 반응을 통해 아민산 백금용액을 제조한 다음, 카본블랙의 연소반응에 대한 촉매 활성을 실험함으로써, 백금족 폐스크랩으로부터 고부가 백금족 화합물의 제조가능성을 연구하였다.

• Bulletin of the Korean Chemical Society
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• 제29권10호
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• pp.1920-1926
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• 2008

We investigated the C-H bond activation mechanism of aldimine by the [RhCl$(PPH_3)_3$] model catalyst using DFT B3LYP//SBKJC/6-31G*/6-31G on GAMESS. Due to their potential utility in organic synthesis, C-H bond activation is one of the most active research fields in organic and organometallic chemistry. C-H bond activation by a transition metal catalyst can be classified into two types of mechanisms: direct C-H bond cleavage by the metal catalyst or a multi-step mechanism via a tetrahedral transition state. There are three structural isomers of [RhCl$(PH_3)_2$] coordinated aldimine that differ in the position of chloride with respect to the molecular plane. By comparing activation energies of the overall reaction pathways that the three isomeric structures follow in each mechanism, we found that the C-H bond activation of aldimine by the [RhCl$(PH_3)_3$] catalyst occurs through the tetrahedral intermediate.