• Journal of Korean Society for Atmospheric Environment
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• v.14 no.4
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• pp.361-368
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• 1998

Acid rainwater samples were collected during 4 years from 1992 in Pusan area nearby seaside. Ionic composition of early and succeeding rainwater were investigated to identify emission sources. pH and Electronic Conductivity of samples were measured immediately after sampling. Major ion concentrations of rain samples were Na+, Ca2+, Mg2+, K+, NH4+, SO42-, NO3-, Cl- which were analyzed by ion Chromatography. 55% of early rainwater and 90% of succeeding rainwater were identified below pH 5.6. Because, Na+, K+, Ca2+ were washed mostly in early rainwater, as a result, pH values were increased by increasing rainfall amounts. It was studied that pH value was varied from ambient ion component, rainfall, and rain intensity. From the principal component analysis result, the dominant components of acid rainwater were Na+, K2+, Mg2+, Ca2+, the elements were contributed soil and marine source, the second components nuts -SO42-, SO4a-, NO3-, nuts -Ca2+ originated from man - made source.

• Proceedings of the Materials Research Society of Korea Conference
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• 2012.05a
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• pp.97.2-97.2
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• 2012

This study examined the utility of two zwitterions, nitrile-functionalized zwitterions and a zwitterion without a nitrile group (MF-ZI), were used as additives along with 1 M $LiPF_6$ in ethylene carbonate (EC):diethylene carbonate (DEC) (3:7 V/V) (E-0) to form an electrolyte solution for use in lithium ion batteries comprising graphite and $LiCoO_2$ electrodes. The presence of NF-ZI (E-NF-ZI) in the electrolyte produced an ion conductivity comparable to that of E-0 and higher than that of an electrolyte containing MF-ZI (E-MF-ZI). Linear sweep voltammetry data revealed that the intensity of the E-NF-ZI reduction peak was lower than that of E-0. Furthermore, the successful formation of an SEI layer in the E-NF-ZI over graphite was confirmed by cyclic voltammetry data. These results were attributed to the adsorption of NF-ZI on the electrode surface, as verified by differential capacity measurements.

• Applied Chemistry for Engineering
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• v.16 no.1
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• pp.144-149
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• 2005

Sulfonated poly(ether ether ketone) (SPEEK) was blended with poly(ether sulfone) (PES) at various compositions. To investigate the possibility of using the blend membranes as polymer electrolyte membranes for direct methanol fuel cell, the blend membranes were characterized in terms of methanol permeability, proton conductivity, ion exchange capacity, and water content. Both proton conductivity and methanol permeability of SPEEK were relatively high. As the amount of PES increased, methanol permeability decreased more rapidly compared to proton conductivity. The experimental results indicated that the blend membrane with 40 wt% PES was the best choice in terms of the ratio of proton conductivity to methanol permeability.

• Korean Journal of Materials Research
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• v.28 no.5
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• pp.308-314
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• 2018

Among the fuel cell electrolyte candidates in the intermediate temperature range, glass materials show stable physical properties and are also expected to have higher ion conductivity than crystalline materials. In particular, phosphate glass has a high mobility of protons since such a structure maintains a hydrogen bond network that leads to high proton conductivity. Recently, defects like volatilization of phosphorus and destruction of the bonding structure have remarkably improved with introduction of cations, such as Zr4+ and Nb5+, into phosphate. In particular, niobium has proton conductivity on the surface because of higher surface acidity. It can also retain phosphorus content during heat treatment and improve chemical stability by bonding with phosphorus. In this study, we fabricate niobium phosphate glass thin films through sol-gel processing, and we report the chemical stability and electrical properties. The existence of the hydroxyl group in the phosphate is confirmed and found to be preserved at the intermediate temperature region of $150-450^{\circ}C$.

• Journal of Electrochemical Science and Technology
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• v.2 no.1
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• pp.26-31
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• 2011

We have prepared siloxane polymers grafted with trifluoromethane-sulfonylamide and oligoether side chains for solid polymer electrolytes with enhanced ionic conductivity. The grafted trifluoromethane sulfonylamide groups seem to be effective as an anion recepting site to enhance the ionic conductivity of the solid polymer electrolyte. The anion receptor grafted siloxane polymers showed one order of magnitude higher ionic conductivity than the siloxane polymers without anion receptor grafts. The fitting parameter A of the VTF plot which was related to the carrier density of the electrolyte increased with increasing the number of grafted anion receptor. The results of experiment indicate that the anion-complexing site of the anion receptor grafted polymer host effectively traps the anions. The anion receptor grafted polymer was found to be a promising material for lithium polymer batteries.

• Transactions of the Korean hydrogen and new energy society
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• v.32 no.6
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• pp.524-533
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• 2021

In this study, a series of anion conductive organic/inorganic composite membranes with excellent ionic conductivity and chemical stability were prepared by introducing graphene oxide (GO) inorganic nanofiller into the quaternized poly(phenylen oxide (Q-PPO) polymer matrix. The fabricated organic/inorganic composite membranes showed higher ionic conductivity than the pristine membrane. In particular, Q-PPO/GO 0.7 showed the highest ionic conductivity value of 143.2 mS/cm at 90℃, which was 1.56 times higher than the pristine membrane Q-PPO (91.5 mS/cm). In addition, the organic/inorganic composite membrane showed superior dimensional stability and alkaline stability compared to the pristine membrane, and the physicochemical stability was improved as the content of inorganic fillers increased. Therefore, we suggest that the as-prepared organic/inorganic composite membranes are very promising materials for anion exchange membrane applications with high conductivity and alkaline stability.

• Journal of Korean Society of Forest Science
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• v.98 no.6
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• pp.712-718
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• 2009

To look into the degree of the long distance movement of the air pollution within Mt. Kyebang, Hongcheon, one of the clean regions, major ions, components of collected wet precipitation, were analyzed by using the ion chromatography after measuring pH and electrical conductivity. The quality assurance of chemical composition data was checked by considering the ion balance and electrical conductivity. Also, the pH of precipitation showed in the pH5.0~5.5 range, less than the pH5.6 in which the standards of the acid precipitation. On the whole, the more precipitation got, the less ion concentration became.: It could showed what it influenced on the fluctuation of the precipitation pH according to fluctuation and neutralization of the according materials. In the meantime, as composition ratios of wet deposition, ${SO_4}^{2-}$ and $nss-{SO_4}^{2-}$, ${NH_4}^+$ and $nss-Ca^{2+}$ accounted for high percentage. Especially, as the concentration of ${SO_4}^{2-}$, the artificial pollutant, and $Ca^{2+}$, the soil substance, showed high, Mt. Kyebang, Hongcheon having barely fixed air-pollutants sources was most likely to be influenced by the pollutants moved from long distances.

• Membrane Journal
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• v.34 no.2
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• pp.154-162
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• 2024

Anion exchange membranes (AEMs) are essential components in water electrolysis systems, serving to physically separate the generated hydrogen and oxygen gases while enabling the selective transport of hydroxide ions between electrodes. Key characteristics sought in AEMs include high ion conductivity and robust chemical and mechanical stability in alkaline. In this study, quaternized Poly(terphenyl piperidinium)/cellulose nanocrystals (qPTP/CNC) mixed matrix membrane was fabricated. The polymer matrix, PTP, was synthesized via super-acid polymerization, known for its excellent ion conductivity and alkaline durability. The qPTP/CNC membrane showed a dense and uniform morphology without significant voids or large aggregates at the polymer-nanoparticle interface. The qPTP/CNC membrane containing 2 wt% CNC demonstrated a high ion exchange capacity of 1.90 mmol/g, coupled with low water uptake (9.09%) and swelling ratio (5.56%). Additionally, the qPTP/CNC membrane showed significantly lower resistance and superior alkaline stability (384 hours at 50℃ in 1 M KOH) compared to the commercial FAA-3-50 membrane. These results highlight the potential of hydrophilic additive CNC in enhancing ion conductivity and alkaline durability of ion exchange membranes.

• Membrane Journal
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• v.27 no.1
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• pp.84-91
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• 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 Korean Electrochemical Society
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• v.6 no.2
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• pp.141-144
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• 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.