• Applied Chemistry for Engineering
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• v.9 no.1
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• pp.115-120
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• 1998

The surface chemistry of $Re_2(CO)_{10}$ deposition for preparing highly dispersed rhenium catalysts and the formation of active site for the metathesis were studied. Alumina as support was treated at 1223K(DA) and 773k(PDA), respectively. The metathesis activity of the catalysts at 298K was measured by using pure propene under atmospheric pressure. The oxidation number of rhenium on PDA was very high, and that on DA was zero-valent with highly dispersed state. The prepared Re/DA catalyst was easily activated by treating with oxygen gas at low temperatures after thermal decomposition at high temperatures. The activity of Re/DA catalyst, even with very low rhenium loading, was much higher than that of Re/PDA or conventional $Re_2O_7/Al_2O_3$ catalysts. Therefore, rhenium carbonyl was effective for preparing a highy active metathesis catalyst with very low rhenium loading. Rhenium ion on Re/DA catalyst seemed to be bonded to two oxygen atoms on DA surface, that is, two-valent. The two-valent rhenium ion was changed to about six-valent by treating with oxygen. It could be considered that propene metathesis occurred through carbene complex which was formed on the six-valent rhenium ions.

• Bulletin of the Korean Chemical Society
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• v.25 no.1
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• pp.79-84
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• 2004

The existing technological schemes for processing rhenium-containing raw materials involve the recovery of Re from solutions, which can be effectively achieved by anion exchange method. The application of anion exchange also allows to study rhenium state in aqueous solutions and to develop analytical control methods. The present work is focused on investigation of ion exchange equilibrium in the analytical system Re(VII)-HCl-$SnCl_2$-KSCN-anion exchanger by means of sorption-desorption method as well as by electron, IR- and diffuse reflection spectroscopy. It was shown that rhenium can be quantitatively recovered from this system. It is proposed to use the sorption-spectroscopic method for Re(VII) determination in aqueous solutions. The calibration curve is linear in the concentration range of 0.5-20.0 mg/L (sample volume is 25.0 mL) and the detection limit is 0.05 mg/L. The presence of Mo(VI), Cu(II), Fe(II, III), Ni(II), Zn(II) as well as $K^+,\;Na^+$ do not hinder the solid-phase determination of rhenium. Rhenium (VII) determination by diffuse reflection spectroscopy was carried out in model solutions as well as in samples of river-derived water and in solutions obtained after the dissolution of spent catalysts.

• Resources Recycling
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• v.18 no.5
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• pp.37-43
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• 2009

The demand for rhenium has considerably increased recently owing to the large-scale consumption in industries and the price of rhenium has increased owing to the lack of supply and its availability. The dust from the roasting of molybdenite was employed to investigate the leaching behavior of rhenium and molybdenum. Leaching experiments were done by varying optimum parameters, such as reaction time, NaOH concentration and leaching temperature. The optimum leaching condition was found to be $4\;mol{\cdot}L^{-1}$ NaOH, 2 hours leaching time, $100\;g{\cdot}L^{-1}$ solid/liquid ratio, $80^{\circ}C$ temperature, and 250 rpm. At this condition, leaching percentage of rhenium and molybdenum was 86.1% and 88.6%, respectively.

• Proceedings of the Korean Nuclear Society Conference
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• 1998.10a
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• pp.301-301
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• 1998

• Bulletin of the Korean Chemical Society
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• v.24 no.4
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• pp.504-506
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• 2003

• Bulletin of the Korean Chemical Society
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• v.27 no.6
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• pp.939-940
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• 2006

• Mass Spectrometry Letters
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• v.1 no.1
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• pp.17-20
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• 2010

As background significantly affects measurement accuracy and a detection limit in determination of the trace amounts of uranium, it is necessary to minimize the impurities in the filaments used for thermal ionization mass spectrometry (TIMS). We have varied the degassing condition such as the heating currents and duration times to reduce the backgrounds from the filaments prepared with zone-refined rhenium tape. The most efficient degassing condition of the heating current and the duration time was determined as 3.5 A and 60 min, respectively. The TIMS measurement combined with the isotope dilution mass spectrometry (IDMS) technique showed that the uranium backgrounds were determined to be in a few fg level from blank rhenium filaments. The background minimized filaments were utilized to measure the uranium isotope ratios of a U030 (NIST) standard sample. The excellent agreement of the measurement with the certified isotope ratios showed that the degassing procedure optimized in this study efficiently reduced the impurity signals of uranium from blank rhenium filaments to a negligible level.

• 한국정보디스플레이학회:학술대회논문집
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• 2007.08b
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• pp.1650-1653
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• 2007

We demonstrate fluorescent green organic lightemitting diodes employing a rhenium oxide ($ReO_3$)-doped N,N-diphenyl-N,N'-bis(1,1'-biphenyl)-4,4'-diamine (NPB) hole transporting layer (HTL). The devices exhibit significantly reduced driving voltages as well as prolonged lifetime. Details of $ReO_3$ doping effects are described in terms of charge transfer complex and stabilization of HTL morphology.

• Bulletin of the Korean Chemical Society
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• v.27 no.5
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• pp.635-636
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• 2006

• Bulletin of the Korean Chemical Society
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• v.23 no.10
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• pp.1439-1444
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• 2002

6-Nitroquipazine has higher binding affinity for SERT than other selective serotonin reuptake inhibitors. We have prepared 6-nitroquipazine based rhenium complexes which would lead to the development of potential SPECT imaging agents with $^{99m}Tc$ for 5-HT transporter.