• 한국재료학회지
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• 제28권11호
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• pp.633-639
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• 2018

In anion exchange membrane fuel cells, Pd nanoparticles are extensively studied as promising non-Pt catalysts due to their electronic structure similar to Pt. In this study, to fabricate Pd nanoparticles well dispersed on carbon support materials, we propose a synthetic strategy using mixed organic ligands with different chemical structures and functions. Simultaneously to control the Pd particle size and dispersion, a ligand mixture composed of oleylamine(OA) and trioctylphosphine(TOP) is utilized during thermal decomposition of Pd precursors. In the ligand mixture, OA serves mainly as a reducing agent rather than a stabilizer since TOP, which has a bulky structure, more strongly interacts with the Pd metal surface as a stabilizer compared to OA. The specific roles of OA and TOP in the Pd nanoparticle synthesis are studied according to the mixture composition, and the oxygen reduction reaction(ORR) activity and durability of highly-dispersed Pd nanocatalysts with different particles sizes are investigated. The results of this study confirm that the Pd nanocatalyst with large particles has high durability compared to the nanocatalyst with small Pd nanoparticles during the accelerated degradation tests although they initially indicated similar ORR performance.

• 한국수소및신에너지학회논문집
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• 제19권2호
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• pp.124-131
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• 2008

Crude cytoplasmic fraction of phototrophic purple sulfur bacterium, Thiocapsa roseopersicina NCIB 8347, were initially prepared and purified by sonication, ultracentrifugation, ammonium sulfate fractionation and heat-treatment and it has been previously reported. Using various applications of chromatography far the purification of membrane-bound and soluble hydrogenases from heat-treated enzyme fraction were studied at present report. When the heat-treated enzyme preparation was applied to the anion column chromatography using Q-sepharose, Fraction I and II, which were extracted with the KCl 0-0.5 M gradient, showed the specific evolution hydrogenase activity 3.86 and 2.27 U/mg-protein respectively. Specific hydrogenase activitys of Fraction I and II were further increased to 4.35 and 7.46 U/mg-protein for Fraction I and to 2.49 and 4.41 U/mg-protein fur Fraction II respectively, when hydrophobic interaction column, Phenyl superose, and anion exchange column, Mono-Q, were applied. Size exclusion chromatography using superdex 200 concentrated the hydrogenase Fraction I and II to 9.19 and 7.84 U/mg-protein respectively at the final step of purification.

• 대한화학회지
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• 제26권5호
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• pp.291-295
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• 1982

Li염이 아미드와 상호작용할 때 카르보닐기와 알킬기의 $^{13}C$chemical shift는 낮은 양쪽으로 이동하였으며, $Li^+$이온이 카르보닐기에 직접 결합함을 보였다. $^{13}C$ chemical shift의 크기는 아미드에 붙어있는 알킬기의 크기뿐만 아니라 음이온과의 상호작용에 의해서 지배됨을 알았다. 전하밀도가 큰 $Cl^-$이온이 $LiClO_4^-$이온보다 큰 음이온 효과를 나타냄을 보인다.

• 한국막학회:학술대회논문집
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• 한국막학회 2004년도 Proceedings of the second conference of aseanian membrane society
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• pp.207-210
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• 2004

The pore-filled anion-exchange membranes were prepared in this study with an asymmetric poly(vinylidene fluoride)(PVDF) membrane as a nascent membrane and poly(vinylbenzyl chloride)(PVBCl) as a polyelectrolyte. The solution of PVBCI having the chloromethylate aryl ring of 80 percents and 1,4-diaminobicyclo [2,2,2]octane(DABCO) was made with the solvent of tetrahydrofuran(THF) and N,N-Dimethylformamide(DMF), which is in the rotio of 8:2. A new preparation method in this study, i.e. in-situ crosslinking, enabled us to produce the pore-filled membranes without change of size, and to control the properties of final membrane with various degree of cross-linking. From the result of surface morphologies of SEM and AFM the polyelectrolyte exists in the pores of nascent membrane as a certain configuration. From the investigation of the solvent affecting much to the permeability and rejection, it was found. that the membranes using DMF and THF showed better performances than the membranes produced by THF only. The water permeability of the final membrane at low pressure(100㎪) showed a typical ultrafiltation membrane's permeability (8-10kg/㎡hr) and good values of rejection(55∼60 percent).

• 전기화학회지
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• 제19권3호
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• pp.107-113
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• 2016

본 연구에서는 고체알칼리 연료전지용 이오노머 바인더 용액 제조를 위하여 poly(2,6-dimethyl-1,4-phenylene oxide)(PPO)를 동결 분쇄하고 4급 암모늄화 반응을 진행하여 음이온 전도성 이오노머(quaternized PPO, QPPO) 용액을 제조하였다. QPPO 이오노머 바인더 용액의 종류를 고분자의 분쇄 시간을 통하여 제조하였고, 이에 따른 분산도, 입자의 크기 및 전기화학적 성능 등을 분석하였다. 이를 통해 기존의 비 분쇄 고분자를 활용하여 제조한 이오노머 바인더 용액보다 분쇄 고분자를 활용한 이오노머 바인더 용액이 높은 고분자 분산도와 낮은 입자 크기를 확보하였다. 제조한 이오노머 바인더 용액(BPPO-G120s)의 최대 이온전도도는 $0.025S\;cm^{-1}$이었으며, 이온교환용량은 $1.26meq\;g^{-1}$을 보였다.

• Bulletin of the Korean Chemical Society
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• 제27권11호
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• pp.1809-1814
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• 2006

The L-Valinate anion coordinating zinc complex, [$Zn(val)_2(H-2O)$], was isolated and structurally characterized by single crystal X-ray crystallography. The crystal possess orthorhombic symmetry with a space group $P2_12_12_1$, Z = 4, and a = 7.4279(2)$\AA$, b = 9.4342(2)$\AA$, c =20.5862(7)$\AA$ respectively. The compound features a penta-coordinate zinc ion in which the two valine anion molecules are directly coordinating the central zinc metal ion via their N (amine) and O (carboxylate) atoms, and an additional coordination to zinc is made by water molecule (solvent) to form a distorted square pyramidal structure. In addition, further synthesis of the valine capped ZnS:Mn nanocrystal from the reaction of [$Zn(val)_2(H-2O)$] precursor with $Na_2S$ and 1.95 weight % of $Mn^{2+}$ dopant is described. Obtained valine capped nanocrystal was water dispersible and was optically characterized by UV-vis and solution PL spectroscopy. The solution PL spectrum for the valine capped ZnS:Mn nanocrystal showed an excitation peak at 280 nm and a very narrow emission peak at 558 nm respectively. The measured and calculated PL efficiency of the nanocrystal in water was 15.8%. The obtained powders were characterized by XRD, HR-TEM, and EDXS analyses. The particle size of the nanocrystal was also measured via a TEM image. The measured average particle size was 3.3 nm.

• 생태와환경
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• 제49권4호
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• pp.289-295
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• 2016

The purpose of this study is to find out the effect of particle size of sediment on adsorption of fluoride. Particle size is classified as sand, silt and clay. Adsorption equilibrium time, adsorption isotherms and the effect of pH were investigated through batch tests. The $pH_{pzc}$ of sand, silt, clay was respectively 6, 8, 4.5 and AEC (anion exchange capacity) was highest in silt, respectively 0.0095, 0.0224, $0.014meq\;g^{-1}$. Adsorption of fluoride on the sediment was in equilibrium within 300 minutes from all particle size. The experimental data of isotherms at various pH were well explained by Freundlich equation. As the experimental results of the effect of pH, the adsorption efficiency of sand and silt were reduced after the $pH_{pzc}$. However, the adsorption efficiency of clay was maintained after the $pH_{pzc}$, and decreased rapidly higher than pH 12.

• Bulletin of the Korean Chemical Society
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• 제30권5호
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• pp.1009-1011
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• 2009

Nano-structured conducting polypyrroles were synthesized in the ionic liquids (ILs) based on 1-alkyl-3-methylimidazolium family with tetrachloroferrate as an anion ($C_n\;mim\;[FeCl_4]\;with\;n\;=\;4,\;8,\;and\;12$). The polypyrrole nanostructures synthesized in ILs were formed as spherical shapes. For ionic liquids with alkyl side chain length $C_4,\;C_4\;mim\;[FeCl_4]$, the size of particles was ranged around 60-nm with a relatively narrow size distribution. As the length of alkyl chain increases, the particle sizes become larger and their distributions become wider. The self-assembled local structures in the solvent ionic liquids are likely to serve as templates of highly organized nano-structured polymers. The length of the alkyl chain in ionic liquids seems to affect these local structures.

• 한국환경보건학회지
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• 제31권4호
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• pp.246-253
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• 2005

The supernatant treatment of recovery process of raw materials of paper plant was studied using DAF (Dissolved Air Flotation) system. We investigated the removal efficiency (COD, SS and turbidity) of the DAF process. The effects of parameters such as A/S ratio, pressure, flotation conditions, coagulant concentration, mixing conditions, size and ratio of packing and nozzle type were examined. The results showed that the optimum A/S ratio and pressure were 0.058 and 4.5-5 atm, respectively. Injection times of pressurized water around 30 s and flotation times around 10 min appeared to be optimal for the DAF operation. Anion polymer addition improved the removal of COD, SS and turbidity. The smaller size and the more packing ratio were enhanced the removal efficiencies. The order of performance of nozzle was full cone > flat > assemble type.

• 청정기술
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• 제21권1호
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• pp.22-32
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• 2015

본 연구에서는 CO₂를 흡수하는 아민용액에서 성능 저하의 원인이 되는 HSS를 제거하기 위해 음이온교환수지를 이용한 HSS의 처리특성을 제시하고자 한다. 최적 HSS 제거효율은 수지 SAR10을 0.05 g/mL 사용할 때 316 K, pH 12에서 96.1%로 나타났다. 또한 최적 수지 재생효율은 NaOH 농도 3 M, 316 K에서 78.8%로 나타났다. HSS의 흡착은 Freundlich 모델에 가장 잘 부합하였으며 흡착 동력 크기를 보았을 때 수지를 이용한 HSS의 제거가 용이한 것으로 나타났다. 흡착 선택계수의 경우 전자가, 원자가가 클수록 높게 나타났고 탈착 선택계수는 이와 반대의 경향을 나타냈다. 연속식 HSS 처리시 오염시료 13.3 BV를 최적으로 처리할 수 있었으며, 5.2 BV가 최적 NaOH 소모량으로 나타났다.