• Applied Chemistry for Engineering
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• v.5 no.6
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• pp.957-966
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• 1994

The transformation of butanes and 1-butene into aromatic compounds was performed over HZSM-5 catalyst and its Ag ion-exchanged form. The yield of aromatic hydrocarbons appreciably increased by incorporating silver cations into HZSM-5. The silver cations serve as catalysts for dehydrogenation of the starting hydrocarbons. $Ag^+$ ions could be reduced to $Ag^0$ metals with resulting in the formation of acidic OH grops by hydrogen produced during the dehydrogenation of butanes and 1-butene. The reaction of 1-butene over ZSM-5 with different loading of Ag was carried out to investigate the effect of acidic properties of these catalysts.

• Proceedings of the Korean Institute of Surface Engineering Conference
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• 1999.05a
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• pp.56-57
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• 1999

• Membrane Journal
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• v.27 no.4
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• pp.313-318
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• 2017

For the separation of olefins/paraffins, $Poly(ethylene oxide)(PEO)/AgBF_4/Al(NO_3)_3/Ag_2O$ composite membranes were prepared. When $Ag_2O$ was introduced, the initial selectivity and permeance of composite membranes were observed to be 13.7 and 21.7 GPU, respectively. The increase in performance compared to the initial performance of $PEO/AgBF_4/Al(NO_3)_3$ membrane (selectivity 13 and permeance 7.5 GPU) was thought to be due to the increase of Ag ion activity due to the addition of $Ag_2O$. However, performance degradation over time was observed, which was thought to be due to the polymer matrix PEO. Since the PEO polymer could not stabilize the $Ag_2O$ particles, the $Ag_2O$ particles becmae aggregated together as the solvent evaporates, and $Ag_2O$ acts as a barrier. As a result, the permeance decreases over time.

• Journal of the Korean Ceramic Society
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• v.34 no.1
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• pp.13-22
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• 1997

Water-soluble phosphate glasses containing Ag and Cu ion were prepared through melting process. Dis-solution characteristics, bactericidal effect and cytotoxicity were investigated with composition and time in D. I. water using the powdered sample. Surface change were observed with increasing dissolution time us-ing the bulk specimen. Dissolution amount was maximum at the molar Ag:Cu ratio of 1 and increased with increasing time. The behavior of dissolution was total dissolution from the early stage. But no new layer was observed at the glass surface during dissolution. The bactericidal effect for pseudomonas sp, e. coli, sta-phylococcus aureus, and salmonella increased with increasing dissolution amount and therefore great bac-tericidal effect appeared. The result of cytotoxicity experiment to L929 showed that solution with more than 10 ppm of Ag ion had strong cytotoxicity.

• Analytical Science and Technology
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• v.20 no.3
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• pp.213-218
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• 2007

Copper(II) ion was measured with the use of a perfluorinated sulfonated polymer-ethylenediamine (nafion-en) modified glassy carbon electrode. The electrode mechanism was based on the chemical reactivity of an immobilized layer (nafion-en) to yield complex $[Cu(en)_2]^{+2}$. The reduction potential peak by differential pulse voltammetry(DPV) was observed at -0.4402V(${\pm}0.0050V$) (vs. Ag/AgCl). The linear calibration curve was obtained from $1.0{\times}10^{-6}$ to $1.0{\times}10^{-4}M$ copper(II) ion concentration, and the detection limit(3s) was $1.96{\times}10^{-6}M$.

• Bulletin of the Korean Chemical Society
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• v.10 no.3
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• pp.234-238
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• 1989

The crystal structure of partially $Ag^+$-exchanged zeolite A, $Ag_{3.2}Na_{8.8}$-A, vacuum dehydrated at $360^{\circ}C$ and then exposed to 0.1 torr of cesium vapor for 12 hours at $250^{\circ}C$ has been determined by single-crystal X-ray diffraction techniques in the cubic space group Pm3m (a = 12.262(2)${\AA})\;at\;21(1)^{\circ}C$. The structure was refined to the final error indexes $R_1=0.068\;and\;R_2=0.072$ by using 338 reflections for which $I_o\;>\;3{\sigma}(I_o)$ and the composition of unit cell is $Ag_{3.2}Cs_{8.8}-A.\;3\;Cs^+$ ions lie on the centers of the 8-rings at sites of D4h symmetry. Two crystallographycally different 6-ring $Cs^+$ ions were found: 1.5 $Cs^+$ ions at Cs(2) are located inside of sodalite cavity and 4.3 $Cs^+$ ions at Cs(3) are located in the large cavity. The fractional occupancies observed at Cs(2) and Cs(3) indicate that the existence of at least three types of unit cells with regard to the 6-ring $Cs^+$ ions. For example, 50% of unit cells may have two $Cs^+$ ions at Cs(2) and 4 $Cs^+$ ions at Cs(3). 30% of unit cells may have one Cs+ ion at Cs(2) and 5 $Cs^+$ ions at Cs(3). The remaining 20% would have one $Cs^+$ ion at Cs(2) and 4 $Cs^+$ ions at Cs(3). On threefold axes of the unit cell two non-equivalent Ag atom positions are found in the large cavity, each containing 0.64 and 1.92 Ag atoms, respectively. A crystallographic analysis may be interpreted to indicate that 0.64 $(Ag_5)^+$ clusters are present in each large cavity. This cluster may be viewed as a tetrasilver molecule $(Ag_4)^0$(bond length, 2.84${\AA}$) stabilized by the coordination of one $Ag^+$ ion.

• Proceedings of the KWS Conference
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• 2006.10a
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• pp.136-138
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• 2006

Recently a lots of problems have observed in high densified and high integrated electronic components. One of them is ion migration phenomena, which induce the electrical short of electrical circuit. Ion migration phenomena has been observed in the field of exposing the specific environment and using for a long time. Also as the RoHS restriction was started in July 1st, 2006, Pb-free solder was utilized in electronics assemblies. In this case, it is very important to compatible between components and printed circuit board(PCB), thus surface treatment materials of PCB was changed to Sn, Sn-3.0Ag-0.5Cu, Cu. Therefore these new application become to need to reevaluate the sensitivity about electrochemical ion migration. This study was evaluated the occurrence time of electrochemical ion migration using by water drop test. We utilized PCB(printed circuit board) having a comb pattern as follows 0.1, 0.318, 0.5, 1.0 mm pattern distance. Sn-3.0Ag-0.5Cu and Sn-37Pb were electroplated on the comb pattern. 6.5V and 15.0V were applied in the comb pattern and then we measured the electrical short time causing by occurring the ion migration. In these results, we evaluate the sensitivity and derived the prediction models of ion migration occurrence time depending on the pattern materials, applied voltage and pattern spacing of PCB conductor.

• Journal of the Korean Chemical Society
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• v.53 no.5
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• pp.609-612
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• 2009

• Korean Journal of Optics and Photonics
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• v.12 no.4
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• pp.320-326
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• 2001

In this paper, we have fabricated asymmetric Y-branch optical power splitters with various optical power splitting ratios by changing the width of one of the output waveguides using $Ag^+-Na^+$ ion change method in BK7 glass. The transmission characteristics of asymmetric Y-branch optical power splitters with different output waveguide width have been investigated using the finitedifference beam propagation method (FD-BPM). We have found the index of the channel waveguide formed by Ag+-Na+ ion change method in BK7 glass and have fabricated channel waveguides to examine the transmission characteristics of channel waveguide. And we have fabricated asymmetric Y-branch optical power splitters with output waveguide width from TEX>$4{\mu}m$ to $6{\mu}m$. /TEX>.

• Bulletin of the Korean Chemical Society
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• v.11 no.5
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• pp.407-410
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• 1990

Three binary ion-exchange isotherms of zeolite A have been determined using 0.1 M solutions of the aqueous nitrates for the one-step preparation of particular mixed-cation zeolite A compositions. Analyses were done primarily by flame emission spectrometry (FES), together with crystallographic determinations of $Cs^+$ and colorimetric determinations of $NH_{4^+}$. Corrections for a presumed impurity of extra-lattice species in powder sample were made for the determination of $Na^+$. The $Cs^+-Ag^+$ isootherm indicates a strong selectivity for $Ag^+$ through the entire range of zeolite composition. The $Ag^+-Na^+$ isotherm agrees very closely with that reported by Sherry and Walton, and that of $NH_{4^+}-Na^+$ resembles those obtained using zeolite pellets.