• Membrane Journal
• /
• v.27 no.1
• /
• pp.84-91
• /
• 2017

In this study, heterogeneous ion exchange membranes were prepared by mixing cation or anion exchange resins and commercial polyvinylidene fluoride (PVDF) for MCDI process. The mixing ratios of PVDF and ion exchange resins were 1 : 1, 1.4 : 1, 2 : 1, and 3 : 1. We characterized SEM, water content, ion exchange capacity, methanol permeability, and ion conductivity. In the viewpoint of membrane characterization, the blending ratio of 2 : 1 showed the best. For the blending ratio of 2 : 1, heterogeneous cation exchange membrane showed the water content 34%, ion exchange capacity 1.54 meq/g, ion conductivity 0.019 S/cm, and methanol permeability $2.28{\times}10^{-7}{\sim}8.86{\times}10^{-7}cm^2/s$ while In the case of heterogeneous anion exchange membrane, the result showed 37%, 2.18 meq/g, and 0.034 S/cm and $1.46{\times}10^{-7}{\sim}8.66{\times}10^{-7}cm^2/s$.

• Journal of the Korea Academia-Industrial cooperation Society
• /
• v.7 no.4
• /
• pp.733-737
• /
• 2006

In this paper, we report the coordination state and structure of $Zn(cyclam)Cl_{2})$ complex that was studied by the Raman spectrum and conductivity method. The complex of zinc(II) ion with 1,4,8,11-tetraazacyclotetradecane(cyclam) ligand is formed in aqueous solution. According to the Raman spectrum of $Zn(cyclam)Cl_{2})$ complex, $H_{2}O$ molecule and $Cl^{-}$ ion compete for the trans coordination site of zinc(II) ion. We also have investigated the competition effect of $H_{2}O$ molecule and $Cl^{-}$ ion by the conductivity method. On addition of 1,4,8,11-tetraazacyclotetradecane(cyclam) ligand to the aqueous $ZnCl_{2}$ solution, 2: 1 electrolyte is changed to 1:1 electrolyte. We suggest the possibility of elimination of heavy metal because of the affinity effect of macrocyclic polyamine(1,4,8.11-tetraazacyclotetradecane) for the heavy metal,.

• Journal of Conservation Science
• /
• v.29 no.4
• /
• pp.421-435
• /
• 2013

The purpose of this study is to suggest environmental guidelines for the conservation of ceramics excavated from underwater. Accordingly, the conditional change of the soluble salt on surface of the excavated ceramics was examined by changing the relative humidity. Examining the relative ratio [high humidity(RH70%+RH80%)/low humidity(RH20%+ RH40%)] for 24 weeks using accumulated conductivity(${\mu}s/cm$), the result showed that the amount of ion elution increased more in high humidity than in low humidity. In particular, the ion elution increased significantly within the celadon sample. In addition, comparing the accumulated conductivity and physical characteristics of the samples in high humidity, the results indicated that the amount of the ion elution is proportioned to the increased rate of the sample's absorption capacity and porosity. Ceramics excavated from underwater has risks of the secondary physical and chemical attacks from remaining salts. Therefore, it is suggested these ceramics be stored in a storage which maintains proper temperature and low humidity conditions. Also, the collections need to be pre-classified according to the properties of the materials.

• Korean Chemical Engineering Research
• /
• v.48 no.6
• /
• pp.731-736
• /
• 2010

In this study, the sulfonated SBS cation-exchange membrane was prepared by post-sulfonation. Degree of sulfonation(DS), water-uptake, ion exchange capacity and electrical resistance and conductivity of sulfonated SBS were investigated as a function of sulfonation time. The DS of sulfonated SBS membrane was increased with increasing the reaction time and concentration of sulfuric acid. The maximum value of DS was 24.0%. And also, the water uptake and ion exchange capacity of the sulfonated SBS membrane were increased as increasing the value of DS. The values of water uptake and IEC were 41.2% and 0.80 meq/g, respectively. The electrical resistance and conductivity of the membrane showed $23.6{\Omega}{\cdot}cm^2$ and $4.24{\times}10^{-4}S/cm$, respectively.

• Journal of the Korean Ceramic Society
• /
• v.38 no.11
• /
• pp.993-999
• /
• 2001

Phase formation and proton conduction in BaO doped LaSc $O_3$with perovskite structure were studied. L $a_{0.6}$B $a_{0.4}$Sc $O_{2.8}$, viz. 40at% $Ba^{2+}$ ion doped composition, showed a single cubic phase, while the other compositions doped less than 30 at% $Ba^{2+}$ ion showed the cubic phase and the orthorhombic one. Above $650^{\circ}C$ oxygen ion conduction was dominant in $N_2$atmosphere and below this temperature proton conduction was observed in wet atmosphere. All compositions were found to be the pure proton conductors below 30$0^{\circ}C$. The proton conductivity (bulk) of L $a_{0.6}$B $a_{0.4}$Sc $O_{2.8}$ was higher than those of any other composition.osition.ion.

• Membrane Journal
• /
• v.21 no.1
• /
• pp.91-97
• /
• 2011

In this study, the anionic exchange membranes were prepared through the impregnation of polyethylenimine (PEI) into porous polyethylene (PE) separator and then crosslinking with isophrhaloyl dichloride (IPC). To characterize the resulting membranes, the contact angles, FT-IR, ion exchnage capacity and ion conductivity were measured. The amide group is produced the reaction between amines in PEI and -COCl in IPC. In case of ion exchange capacity, 1.96 meq./g dry membrane at the reaction time, 30 sec was decreased to 1.14 meq./g dry membrane at 600 sec reaction time. The ion conductivity, $9.15{\times}10^{-2}S/cm$ at 30 sec reaction time, was obtained.

• Polymer(Korea)
• /
• v.35 no.6
• /
• pp.586-592
• /
• 2011

In this study, we synthesized vinylbenzyl chloride-co-styrene-co hydroxyethyl acrylate (VBC-co-St-co-HEA) copolymer that can be applied to redox the flow battery process. The anion exchange membrane was prepared by the amination and crosslinking of VBC-co-St-co-HEA copolymer. The chemical structure and thermal properties of VBC-co-St-co-HEA copolymer and aminated VBC-co-St-co-HEA(AVSH) membrane were characterized by FTIR, $^1H$ NMR, TGA, and GPC analysis. The membrane properties such as ion exchange capacity(IEC), electrical resistance, ion conductivity and efficiency of all-vanadium redox flow battery were measured. The IEC value, electrical resistance, and ion conductivity were 1.17 meq/g, $1.9{\Omega}{\cdot}cm^2$, 0.009 S/cm, respectively. The charge-discharge efficiency, voltage efficiency and energy efficiency from all-vanadium redox flow battery test were 99.5, 72.6 and 72.1%, respectively.

• Journal of the Korean Electrochemical Society
• /
• v.24 no.4
• /
• pp.93-99
• /
• 2021

In order to decrease the weight of stretchable energy storage devices, interest in developing lightweight materials to replace metal current collectors is increasing. In this study, nanofibers prepared by electrospinning a conductive polymer, PEDOT:PSS, were used as current collectors for lithium ion batteries. The nanofiber showed improved electrical conductivity by using DMSO, a dopant, and indicated a stretch rate of 30% or more from the elasticity evaluation result. In addition, the use of the nanofiber current collector facilitates penetration of the liquid electrolyte and exhibits the effect of increasing the electronic conductivity through the nanofiber network. The lithium-ion battery using the DMSO-doped PEDOT:PSS@PAM nanofiber current collector indicated a high discharge capacity of 135mAh g^-1, and indicated a high capacity retention rate of 73.5% after 1000 cycles. Thus, the excellent electrochemical stability and mechanical properties of conductive nanofibers showed that they can be used as lightweight current collectors for stretchable energy storage devices.

• Journal of the Korean Electrochemical Society
• /
• v.6 no.2
• /
• pp.141-144
• /
• 2003

Proton conducting polymeric gels as the electrolytes of electrochemical capacitors have been prepared by two different methods: 1) swelling a polymethacrylate-based polymer matrix in aqueous solutions of inorganic and organic acids, and 2) polymerizing complexes of anhydrous acids and prepolymers with organic plasticizer. The FT-IR spectra strongly suggest that the carbonyl groups in the polymer matrix interact with protons from the doped acids. High ionic (proton) conductivity in the range of $6\times10^{-4}-4\times10^{-2}\;S\;cm^{-1}$ was obtained at room temperature for the aqueous gels. The non-aqueous polymer complexes showed rather low ionic conductivity, but it was about $10^{-3}\;S\;cm^{-1}\;at\;70^{\circ}C$ for the $H_3PO_4$ doped polymer electrolyte. The mechanisms of ion (proton) conduction in the polymeric systems are discussed.

• Bulletin of the Korean Chemical Society
• /
• v.32 no.6
• /
• pp.2039-2044
• /
• 2011

A semi-continuous and automated method for quantifying atmospheric ammonia at the parts per billion level has been developed. The instrument consists of a high efficiency diffusion scrubber, an electrolytic on-line anion exchange device, and a conductivity detector. Water soluble gases in sampled air diffuse through the porous membrane and are absorbed in an absorbing solution. Interferences are eliminated by using an anion exchange devises. The electrical conductivity of the solution is measured without chromatographic separation. The collection efficiency was over 99%. Over the 0-200 ppbv concentration range, the calibration was linear with $r^2$ = 0.99. The lower limit of detection was 0.09 ppbv. A parallel analysis of Seoul air over several days using this method and a diffusion scrubber coupled to an ion chromatography system showed acceptable agreement, $r^2$ = 0.940 (n = 686). This method can be applied for ambient air monitoring of ammonia.