• Carbon letters
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• v.8 no.3
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• pp.199-206
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• 2007

The activated carbon produced from rubber wood sawdust by chemical activation using phosphoric acid have been utilized as an adsorbent for the removal of Cu(II) from aqueous solution in the concentration range 5-40 mg/l. Adsorption experiments were carried out in a batch process and various experimental parameters such as effect of contact time, initial copper ion concentration, carbon dosage, and pH on percentage removal have been studied. Adsorption results obtained for activated carbon from rubber wood sawdust were compared with the results of commercial activated carbon (CAC). The adsorption on activated carbon samples increased with contact time and attained maximum value at 3 h for CAC and 4 h for PAC. The adsorption results show that the copper uptake increased with increasing pH, the optimum efficiency being attained at pH 6. The precipitation of copper hydroxide occurred when pH of the adsorbate solution was greater than 6. The equilibrium data were fitted using Langmuir and Freundlich adsorption isotherm equation. The kinetics of sorption of the copper ion has been analyzed by two kinetic models, namely, the pseudo first order and pseudo second order kinetic model. The adsorption constants and rate constants for the models have been determined. The process follows pseudo second order kinetics and the results indicated that the Langmuir model gave a better fit to the experimental data than the Freundlich model. It was concluded that activated carbon produced using phosphoric acid has higher adsorption capacity when compared to CAC.

• Journal of the Korean Magnetic Resonance Society
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• v.20 no.3
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• pp.76-81
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• 2016

Copper is an elemental ion in living organisms. CopP from Helicobacter Pylori (HpCopP) is a copper(I)-binding protein and was suggested as regulator of copper metabolism in vivo. Previously, the metal binding property of HpCopP for Ag(I), Cu(I), and Cu(II) as well as the tertiary structure of HpCopP was shown. In this study, the dynamic profiles of HpCopP depending on metal binding were studied using ${^1H}-^{15}N$ steady-state NOE analysis. The heteroNOE experiment was performed for apo-CopP or metal-bound CopP. The obtained NOE values were analyzed and compared to figure out the effect of metals on the structural flexibility of HpCopP. As a result, Ag(I) and Cu(I) ions improved the rigidity of the structure while Cu(II) ion increased the flexibility of the structure, suggesting the oxidation of the CXXC motif decreases the structural stability of HpCopP.

• Journal of Wetlands Research
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• v.20 no.4
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• pp.410-416
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• 2018

This experiment was carried out with the purpose of testing nickel and copper adsorption abilities of multi wall carbon nanotube (MWCNT) and activated carbon. In the acidic condition, only MWCNT was effective for removing nickel and copper ion in the aqueous phase while activated carbon rarely remove them. The MWCNT and heavy metals adsorption reaction followed pseudo-first order kinetic. When the initial pH value was neutral (pH=7), nickel was rapidly removed by MWCNT and activated carbon in 4 hr (99.02 %, 80.30 %). Also, copper ion was rapidly removed by both adsorbents in 4 hr when the initial pH was 7 (100 %, 99.73 %). Increasing of adsorbent dosages affect the pH evolution and heavy metal ions removal (0 ~ 99%). Also, oxidation pretreatment enhanced the adsorption efficiency of MWCNT.

• Proceedings of the Korean Institute of Surface Engineering Conference
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• 2016.11a
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• pp.124.1-124.1
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• 2016

In this work, uniform thickness and good adhesion of electrodeposited copper layer were achieved on AZ91 Mg alloy in alkaline noncyanide copper solution containing pyrophosphate ion by employing appropriate zincate pretreatment. Without zincate pretreatment, the electrodeposited copper layer on AZ91 Mg alloy was porous and showed poor adhesion which was explained by small number of nucleation sites of copper due to rapid dissolution of the magnesium substrate in the pyrophosphate solution. The zincate pretreatment was found as one of the most important steps that can form a conducting layer to cover AZ91 surface which decreased the dissolution rate of AZ91 Mg alloy about 40 times in the copper pyrophosphate solution. Electrodeposited copper layer on AZ91 Mg alloy after an appropriate zincate pretreatment showed good adhesion and uniform thickness with bright surface appearance, independent of the deposition time but the surface roughness of the electrodeposited copper layer increased with increasing Cu deposition time.

• Journal of Korean Society on Water Environment
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• v.27 no.1
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• pp.54-60
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• 2011

To evaluate the feasibility of electrodialysis for copper removal from industrial wastewater, the effect of operating parameters on the removal of copper was experimentally estimated. The limiting current density (LCD) linearly increased with the copper concentration and the flow rate. The time when the copper concentration of diluate reaches to 3 mg/L was linearly proportional to initial concentration of diluate, and the concentration of concentrate did not affect the removal rate. Increase in the flow rate gave a positive effect on the removal rate and became insignificant at flow rates greater than 2.4 L/min. The removal rate increased with the applied voltage. From the operation of the electrodialysis module used in this research, the flow rate of 2.4 L/min and the voltage corresponding to the 80~90% of LCD were found be the optimum operating condition for the copper removal from highly concentrated copper solutions.

• Journal of the Korean Chemical Society
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• v.23 no.2
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• pp.88-93
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• 1979

The adsorption of propylene on copper(II)-exchanged zeolite Y was studied by temperature programmed desorption (TPD) technique and electron spin resonance. The amount of propylene adsorbed increased with increasing copper ion content. Four TPD peaks with desorption temperature maxima at $108^{\circ}C({\alpha})$, $243^{\circ}C({\beta})$, $284^{\circ}C({\gamma})$ and $420^{\circ}C({\delta})$ were observed (heating rate: $6.4^{\circ}C$/min). ${\alpha}$Peak which was also observed in the TPD of propylene from NaY may be assigned to propylene physically adsorbed on the zeolite surface, ${\beta}$ and ${\gamma}$ peaks to the chemisorbed propylene either on copper ion or Bronsted acid site produced by copper ion, and $\delta$ peak to cracking products from the polymeric material formed from propylene adsorbed.

• Journal of the Mineralogical Society of Korea
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• v.27 no.4
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• pp.293-299
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• 2014

The bentonite, a buffer material, is essential for the deep geological disposal of HLW (high-level radioactive waste), and it is important to know its characteristic long-term evolution in the underground environment. With an assumption that the concentration of aqueous copper ions will increase if copper-coated materials on a metal canister are corroded, we examined some characteristic ion-exchanges and cation release phenomena occurring in the bentonite clay (montmorillonite) interacted with aqueous Cu cations. During the interaction between dissolved copper and bentonite, Na rather than Ca cations in the expandable clay were preferentially replaced by Cu ions in the experiment. In addition, the Cu-exchanged montmorillonite was characterized by an asymmetric X-ray diffracted pattern with relatively collapsed interlayers compared to the raw sample. These results indicate that the gradual change of the original bentonite property may occur in a underground disposal condition. We are going to further study the characteristic chemical and mineralogical changes of the bentonite buffer to be used for the disposal site by conducting additional experiments.

• Analytical Science and Technology
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• v.8 no.4
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• pp.611-615
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• 1995

The design of appropriate chemically modified electrodes should allow development of new voltammetric measurement schemes with enhanced selectivity and sensitivity. Microorganism like algae has high ability to trap toxic and heavy metal ions and different affinities for metal ions. A copper(II) ion-selective carbon paste electrode was constructed by incorporating alga Anabaena into a conventional carbon paste mixture, and then the film of 10% Nafion was coated to avoid the swelling of the electrode surface. Copper ion could be deposited at the 25% algamodified electrode for 15 min without the applied potential while stirring the solution by only immersing the electrode in a buffer (pH 4.0) cot1taining copper(II). Temperature was controlled at $35^{\circ}C$. After preconcentration was carried out the electrode was transferred to a 0.1 M potassium chloride solution and was reduced at -0.6 volt at $25^{\circ}C$. The differential pulse anodic stripping voltammetry was employed. A well-defined oxidation peak could be obtained at -0.1 volt (vs SCE). In five deposition / measurement / regeneration cycles, the responses were reproducible and relative standard deviations were 3.3% for $8.0{\times}10^{-4}M$ copper(II). Calibration curve for copper was linear over the range from $2.0{\times}10^{-4}M$ to $1.0{\times}10^{-3}M$. The detection limit was $7.5{\times}10^{-5}M$. Studies of the effect of diverse ions showed that the coexisting metal ions had little or no effect for the determination of copper. But anions such as cyanide. oxalate and EDTA seriously interfered.

• Bulletin of the Korean Chemical Society
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• v.27 no.10
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• pp.1593-1596
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• 2006

The polymeric membrane electrodes based on N,N'-bis-pyridin-2-ylmethylene-naphthalene-1,8-diamine as an ion carrier were prepared and tested for the copper-ion selective electrode. The membrane has a linear dynamic range between $10^{-6}$ and $10^{-2}$ M with a Nernstian slope of 29.6 mV per decade, and its detection limit was $10^{-5.62}$M. The potentiometric response is independent of the pH range of 3-5. The proposed electrode showed good selectivity and response for $Cu^{2+}$ over a wide variety of other metal ions in pH 4.0 buffer solutions.

• Journal of Korean Society for Atmospheric Environment
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• v.7 no.2
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• pp.137-142
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• 1991

A method is developed for the simultaneous determination of dissolved iron, copper, and zinc in rainwater. The method involves 25-fold evaporative concentration, ion chromatographic separation and subsequent spectrophotometric detection after post-column reaction with 4-(2-pyridylazo) resorcinol. Analytical sensitivities, being defined by the slopes of calibration curves, are 0.93, 0.54, and 0.11 Abs/ $\mu$g/ml for iron, copper, zinc, respectively. Detection limits render around a few tenth of one ng/ml. Precisions evaluated by replicate analysis of real sample are better than 10% RSD. Due to the lack of certified standards for rainwater, the accuracy of the method could not be assessed directly. However, the results of this method agree well with those by inductively coupled plasma mass spectrometry. Analytical results for a suite of Seoul rainwaters are presented herein.