• 제목/요약/키워드: Ionic Fraction

검색결과 86건 처리시간 0.02초

Microstructure and shear modulus in concentrated dispersions of bidisperse charged spherical colloids

  • Chun, Myung-Suk;Lee, Sangwoo;Lee, Tae-Seok;Cho, Jae-Seol
    • Korea-Australia Rheology Journal
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    • 제16권1호
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    • pp.17-26
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    • 2004
  • We examine rigorous computations on microstructural as well as rheological properties of concentrated dispersions of bidisperse colloids. The NVT Monte Carlo simulation is applied to obtain the radial distribution function for the concentrated system. The long-range electrostatic interactions between dissimilar spherical colloids are determined using the singularity method, which provides explicit solutions to the linearized electrostatic field. The increasing trend of osmotic pressure with increasing total particle concentration is reduced as the concentration ratio between large and small particles is increased. From the estimation of total structure factor, we observe the strong correlations developed between dissimilar spheres. As the particle concentration increases at a given ionic strength, the magnitude of the first peak in structure factors increases and also moves to higher wave number values. The increase of electrostatic interaction between same charged particles caused by the Debye screening effect provides an increase in both the osmotic pressure and the shear modulus. The higher volume fraction ratio providing larger interparticle spacing yields decreasing high frequency limit of the shear modulus, due to decreasing the particle interaction energy.

Novel Composite Membranes Comprising Silver Salts Physically Dispersed in Poly(ethylene-co-propylene) for the Separation of Propylene/Propane

  • Kim, Jong-Hak;Min, Byoung-Ryul;Kim, Yong-Woo;Kang, Sang-Wook;Won, Jong-Ok;Kang, Yong-Soo
    • Macromolecular Research
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    • 제15권4호
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    • pp.343-347
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    • 2007
  • Novel composite membranes, which delivered high separation performance for propylene/propane mixtures, were developed by coating inert poly(ethylene-co-propylene) rubber (EPR) onto a porous polyester substrate, followed by the physical distribution of $AgBF_4$. Scanning electron microscopy-wavelength dispersive spectrometer (SEM-WDS) revealed that silver salts were uniformly distributed in the EPR layer. The physical dispersion of the silver salts in the inert polymer matrix, without specific interaction, was characterized by FT-IR and FT-Raman spectroscopy. The high separation performance was presumed to stem from the in-situ dissolution of crystalline silver ionic aggregates into free silver ions, which acted as an active propylene carrier within a propylene environment, leading to facilitated propylene transport through the membranes. The membranes were functional at all silver loading levels, exhibiting an unusually low threshold carrier concentration (less than 0.06 of silver weight fraction). The separation properties of these membranes, i.e. the mixed gas selectivity of propylene/propane ${\sim}55$ and mixed gas permeance ${\sim}7$ GPU, were stable for several days.

Facile preparation of self-assembled wool-based graphene hydrogels by electron beam irradiation

  • Park, Mira;Pant, Bishweshwar;Choi, Jawun;Park, Yong Wan;Lee, Chohye;Shin, Hye Kyoung;Park, Soo-Jin;Kim, Hak-Yong
    • Carbon letters
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    • 제15권2호
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    • pp.136-141
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    • 2014
  • Three dimensional self-assembled graphene hydrogels were easily fabricated by electron beam irradiation (EBI) using an aqueous solution of wool/poly(vinyl alcohol) and graphene oxide (GO). After exposure to various levels of EBI radiation, the highly porous, self-assembled, wool-based graphene hydrogels were characterized using scanning electron microscopy and Fourier-transform infrared spectroscopy; to determine the gel fraction, degree of swelling, gel strength, kinetics-of-swelling analyses and removal of hexavalent chromium (Cr(VI)) from the aqueous solution. X-ray diffraction results confirmed that EBI played a significantly important role in reducing GO to graphene. The adsorption equilibrium of Cr(VI) was reached within 80 min and the adsorption capacity was dramatically increased as the acidity of the initial solution was decreased from pH 5 to 2. Changes in ionic strength did not exert much effect on the adsorption behavior.

Operating Parameters for Glutamic Acid Crystallization in Displacement Ion Exchange Chromatography

  • Lee, Kisay
    • Biotechnology and Bioprocess Engineering:BBE
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    • 제2권2호
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    • pp.117-121
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    • 1997
  • Glutamic acid can be crystallized inside cation exchange column when displacer NaOH concentration is high enough to concentrate displaced glutamic acid beyond its solubility limit. Resulting crystal layer of glutamic acid was moved with liquid phase through the column, and thus could be eluted from the column and recovered in fraction collector. For the purpose of enhancing crystal recovery, effects of operating parameters on the crystal formation were investigated. The increase in the degree of crosslinking of resin favored crystal recovery because of its low degree of swelling. Higher concentration of displacer NaOH was advantageous. If NaOH concentration is too high, however, crystal recovery was lowered due to the solubility-enhancing effects of high pH and ionic strength. The decrease of mobile phase flow rate enhanced crystal recovery because enough time to attain local equilibrium could be provided, but film diffusion would control the overall crystal formation with extremely low flow rate. Lower temperature reduced solubility of glutamic acid and thus favored crystal formation unless the rate of ion exchange was severely reduced. The ion exchange operated by displacement mode coupled with crystallization was advantageous in reducing the burden of further purification steps and in preventing purity-loss resulted from overlapping between adjacent bands.

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제주도 고산에서의 1994년 여름 측정: (I) 입자 이온 조성 (Measurements at Kosan, Cheju Island during the Summer, 1994: (I) Aerosol Ion Composition)

  • 김용표;김성주;진현철;백남준;이종훈;김진영;심상규;강창희;허철구
    • 한국대기환경학회지
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    • 제12권3호
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    • pp.297-305
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    • 1996
  • Aerosol measurements were carried out at Kosan, Cheju Island, Korea for the period from July 20 to August 10, 1994. Total suspended particles were collected by high volume samplers and PM 2.5 particles with gaseous volatile species were collected by a filter pack sampler and their ionic composition are analyzed. The average mass concentration of PM 2.5 particles was comparable to that of PM 3 particles collected during March, 1994 at the same site but the average non sea-salt sulfate concentration was higher that that of PM 3 particles, implying the fraction of anthropogenic air apllutants during this period is higher than that during March, 1994. During the measurement period, two distincitive patterns were observed, high concentrations of mass and water soluble ions were observed between July 20 and August 1 while those during after August 2 were low. Back trajectory analysis results show that air masses arriving at Kosan during the earlier period were mainly from Korea and Japan while those during the later period were from the North Pacific Ocean. It is suggested that the particle ion concentrations during the later period are marine background concentrations at Kosan during the summertime.

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Methanol-물 및 2-Propanol-물의 混合溶媒에서의 Hydrogen Cupferrate의 酸解離常數의 決定 (Determination of Dissociation Constant of Hydrogen Cupferrate in Methanol-Water and 2-Propanol-Water Solution)

  • 김시중;윤창주;장인순
    • 대한화학회지
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    • 제10권3호
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    • pp.119-128
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    • 1966
  • The glass electrode was empirically calibrated in methanol-and 2-propanol-water mixed solvents, by means of which the pH-meter reading could be converted to stoichiometric hydrogen ion concentration. The thermodynamic dissociation constants of hydrogen cupferrate in methanol-and 2-propanol-water solution were potentiometrically determined with the changes in composition of organic solvents at 0.01 and 0.05 of the ionic strength and 25$^{\circ}C$. The empirical formula of the constants with mole fraction (n) of the organic solvent are as follow: methanol-water solution $pK_a$= 2.24n + 4.29 at ${\mu}$ = 0.01 n = 0.0476∼0.642 $pK_a$ = 2.35n + 4.38 at ${\mu}$ = 0.05 n= 0.0446~0.642 2-propanol-water solution $pK_a$= 5.50n + 4.48 at ${\mu}$ = 0.05 n = 0.0253~0.259 The relationships between $pK_a$ of acetic acid, propionic acid and HCup and dielectric constant of some mixed solvents were discussed. It would be considered that the factors effecting $pK_a$ value of weak acid in mixed-solvent are not only dielectric constants but acid-base character and solvation effect of the solvent, etc.

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Selective Coordination of Silver Ions to Poly(styrene-b-(ethylene-co-butylene)-b-styrene) and its Influence on Morphology and Facilitated Olefin Transport

  • Lee, Dong-Hoon;Kang, Yong-Soo;Kim, Jong-Hak;Kang, Sang-Wook
    • Macromolecular Research
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    • 제16권8호
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    • pp.676-681
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    • 2008
  • The $\pi$-complex membranes of poly(styrene-b-(ethylene-co-butylene)-b-styrene) (SEBS) of two silver salts of $AgBF_4$ and $AgCF_3SO_3$ were prepared and tested for the separation of the propylene/propane mixtures. The Fourier-transform infrared (FT-IR) spectra of these complexes showed that the silver salts were dissolved in SEBS up to a silver mole fraction of 0.14, due to $\pi$-complexation between the aromatic C=C bonds of styrene blocks and silver ions. Above this solubility limit, ion pairs and high-order ionic aggregates began to form, so that silver salts were distributed unselectively in both the EB and PS blocks. The domain size of the PS blocks was enlarged up to this critical concentration with increasing silver concentration without structural transitions, as confirmed by small angle x-ray scattering (SAXS). These structural properties of the SEBS/silver salt complexes may explain the lower separation properties for propylene/propane mixtures compared to poly(styrene-b-butadiene-b-styrene)(SBS)/silver salt complex membranes.

Pridiction of Adsorption Equilibrium for Binary Gas Mixtures on Cation Exchanged Forms of ZSM-5

  • Going Yim;Chai Suck Yim
    • 공학논문집
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    • 제6권2호
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    • pp.85-98
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    • 2004
  • The adsorption equilibrium data for the binary gas mixture system from the pure gas adsorption data of carbon dioxide and ethylene on ZSM-5 prepared were predicted. The binary gas mixture adsorption data have been examined against predicted values by two models-the vacancy solution model(VSM) and the statistical thermodynamic model(STM), using parameters obtained from the single component isotherm. The binary gas mixture data for the carbon dioxide-ethylene system were obtained for cation exchanged forms of ZSM-5 for the gas phase carbon dioxide mole fraction of 0.752 at $37^{\circ}C$ and 1 atm. The experimental adsorption phase diagrams were obtained for carbon dioxide-ethylene on sodium form ZSM-5 synthesized. The single component adsorption isotherms for carbon dioxide and ethylene were also obtained for this zeolite. The single component data were used to obtain parameters derived in two models. These parameters were, in turn, used to predict the binary mixture isotherms for this zeolite. Both the vacancy solution and the statistical thermodynamic models give satisfactory predictions of adsorption phase diagrams for the binary gas mixtures of carbon dioxide and ethylene on sodium exchanged ZSM-5. Also the correlation between the experimental data and the predicted values is generally in good agreement. The system appears to show ideal behavior with a relatively constant separation factor. The slight increase in adsorption capacity with an increase in ionic radius is due, in part, to the higher polarizability associated with larger cations.

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고분자 전해질 멤브레인용 하이드로퀴논 부분이 포함된 설폰화된 폴리(아릴렌 비페닐설폰 에테르) 공중합체의 합성과 특성평가 (Synthesis and characterization of sulfonated poly(arylene biphenylsulfone ether) copolymers containing hydroquinone moiety for polymer electrolyte membrane)

  • 유동진
    • 에너지공학
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    • 제19권2호
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    • pp.121-127
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    • 2010
  • 본 연구에서는 4,4'-bis[(4-chlorophenyl)sulfonyl]-1,1'-biphenyl(BCPSBP), 술폰화된 하이드로퀴논, 4,4'-sulfonyldiphenol를 이용하여 새로운 폴리(아릴렌 비페닐설폰 에테르) 공중합체를 합성하였고 이들의 특성을 평가하였다. 첨가한 술폰화된 하이드로퀴논의 몰분율에 따라 PBPSEH-HQ00, PBPSEH-HQ10, PBPSEH-HQ30의 고분자전해질막을 합성하였다. 제조한 공중합체의 구조분석은 NMR, IR, GPC를 사용하여 실시하였고, GPC에서 평균분자량은 62,000-213,000 g $mol^{-1}$이며, 이때 PDI는 1.66-4.04였다. TGA와 DSC를 통하여 열분석을 실시하였고, 고분자의 이온화정도가 많아짐에 따라 $T_{d5%}$$T_{d10%}$는 낮아 졌으며, $T_g$값은 점점 상승하였다. 함습율과 IEC, 이온전도도는 술폰화된 하이드로퀴논 몰분율이 증가함에 따라 증가하였다. 고분자전해질막에서 중요한 양이온 전도도는 $60^{\circ}C$ 및 100%상대습도에서 약 9.4 mS $cm^{-1}$이었다. 측정된 결과로부터 본 연구에서 제조한 탄화수소계 멤브레인은 연료전지용 고분자전해질막으로 사용될 수 있다.

2009-2014년 제주지역 강수의 이온조성 및 오염특성 (Ionic composition and pollution characteristics of precipitation in Jeju Island during 2009-2014)

  • 부준오;송정민;신수현;김원형;강창희
    • 분석과학
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    • 제29권1호
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    • pp.19-28
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    • 2016
  • 2009~2014년에 제주지역의 강수시료(n=284)를 채취하여 주요 이온 성분을 분석하였다. 분석 정확도 확인을 위해 이온수지, 전기전도도, 산분율 비교법으로 회귀분석을 실시한 결과, 이들의 상관계수는 0.927~0.983의 범위로 양호한 직선성을 나타내었다. 강수의 부피가중평균 pH 4.9, 전기전도도는 22.7 µS/cm, 이온세기는 0.27±0.38 mM로 시료 중 약 35.9 %가 순수한 빗물 수준을 보였다. 강수 이온성분의 부피가중 평균농도(µeq/L)는 Na+ > Cl > nss-SO42− > NO3 > NH4+ > Mg2+ > H+ > nss-Ca2+ > PO43− > K+ > HCOO > CH3COO > NO2 > F > HCO3 > CH3SO3 순이었다. 강수의 산성화 기여율은 황산과 질산의 기여율이 각각 54.5 %, 36.5 %인 반면에 유기산 음이온인 HCOO 와 CH3COO 의 기여율은 각각 4.8 %, 4.2 %를 나타내어 제주지역 강수의 산성화는 유기산보다는 주로 무기산에 의해 일어나고 있음을 확인할 수 있었다. 또한 중화인자를 확인한 결과, NH3에 의한 중화인자는 33 %를 나타내었고 CaCO3에 의한 중화인자는 20 % 이었다.