• 제목/요약/키워드: aqueous electrolyte

검색결과 246건 처리시간 0.027초

전착법에서 용액특성이 지르코니아 막형성에 미치는 영향 (Effect of Slurry Property on Preparation of Zirconia Film in Electrophoretic Deposition)

  • 김상우;이병호;손용배;송휴섭
    • 한국세라믹학회지
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    • 제36권9호
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    • pp.991-996
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    • 1999
  • Effect of solution property on the weight varation and microstructural change of film was studied by electrophoretic deposition in order to obtain a homogeneous and dense zirconia film. As a result of weight kinetics of film which obtained in alcohol or aqueous solution having different polarity experimental data showed large deviation from theoretical ones calculated by Zhang's kinetic model. It had been shown that the weight affecting factors was largely dependent on properties other than dielectric constant and viscosity of solvent zeta potential appiled field and time. In initial stage a main factor of the drastic weight increase was the capillary drag of porous substrate. The cause of weight decrease with time in aqueous solution after 300 s was attributed to the defect of film by sagging and electrolytic reaction. The electrolyte film which prepared in alcohol solution with good wetting for substrate had better homogeneous and dense microstructure than one in aqueous solution with high surface tension.

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Kinitics of Thixotropy of Aqueous Bentonite Suspension

  • Kisoon Park;Taikyue Ree
    • 대한화학회지
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    • 제15권6호
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    • pp.293-303
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    • 1971
  • The theological properties of aqueous suspensions of Black Hills bentonite were measured by using a Couette-type viscometer. Three kinds of flow units in aqueous bentonite suspension were postulated. Each has a different average relaxation time, one Newtonian. One of the non-Newtonian types is thixotropic, and the other is non-thixotropic. The thixotropic non-Newtonian unit is transformed to a Newtonian unit by shear stress. If the stress is relieved, the transformed unit returns to its original state. Two flow equations were derived by introducing chemical kinetics consideration for such a transition into the generalized theory of viscous flow. One equation describes the "upcurve," a diagram of rate of sheat versus shear stress, obtained by increasing the rate of shear, and the other relates to the "downcurve" obtained by decreasing the shear rate. The equations satisfactorilly describe the experimental thixotropic hysteresis of bentonite suspensions. The equations also were successfully applied to the flow curves of the suspensions containing various amounts of monovalent electrolyte (KCI).

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Effects of Electrolytes in a Liquid Thin Layer System

  • Chung, Taek-Dong
    • 전기화학회지
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    • 제5권4호
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    • pp.216-220
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    • 2002
  • The effects of electrolytes on electrochemical behavior from an oil thin layer interposed between a graphite electrode and an aqueous solution phase were examined. A hydrophobic electroactive species, tetrachloro-1,4-benzoquinone (TCQ), in a benzonitrile (EN) layer was employed to study ion transfer properties across the BN-water interface. Experimental results showed that hydrophobic cations as well as anions could be successfully used as ionic charge carriers. The addition of various salts into either the oil layers or the aqueous solutions offers deeper insight for the electrochemistry of the liquid thin layer system. When aqueous perchloric acid is interfaced with the BN films, the perchlorate ion of tetrahexylammonium perchlorate (THAP) substantially suppresses the dissociated proton concentration in the layer by the common ion effect while there is only a little change in the total acid concentration. Further approach by theoretical calculation makes it possible to quantitatively understand the effect of the electrolytes to the electrochemical responses of TCQ, which were previously reported (Anal. Chem. 73, 337 (2001)).

전해질 수용액의 고온 열역학 (High Temperature Thermodynamics of Aqueous electrolyte Solutions)

  • 이만승
    • 자원리싸이클링
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    • 제27권2호
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    • pp.63-67
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    • 2018
  • 자유에너지는 물질의 상대적인 안정도를 나타낸다. 수용액에 존재하는 이온의 종류는 다양하고 실험조건이 광범위하므로 열역학 자료가 부족하다. 이온의 표준생성엔탈피와 엔트로피로부터 표준수화엔탈피와 표준수화엔트로피의 절대값과 상대값을 구하는 방법을 설명하였다. 또한 대응원리를 이용하여 고온에서 열역학 자료를 추산하는 방법을 설명하였다.

고체 고분자 전해질(SPE)을 이용한 전기분해 공정에서 Rhodamine B 분해 (Degradation of Rhodamine B in Water using Solid Polymer Electrolyte (SPE) in the Electrolysis Process)

  • 박영식
    • 한국환경보건학회지
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    • 제40권2호
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    • pp.137-146
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    • 2014
  • Objectives: Feasibility of electrochemical oxidation of the aqueous non-biodegradable wastewater such as cationic dye Rhodamine B (RhB) has been investigated in an electrochemical reactor with solid polymer electrolyte (SPE). Methods: Nafion 117 cationic exchange membrane as SPE has been used. Anode/Nafion/cathode sandwiches were constructed by sandwiching Nafion between two dimensionally stable anodes (JP202 electrode). Experiments were conducted to examine the effects of applied current (0.5~2.0 A), supporting electrolyte type (0.2 N NaCl, $Na_2SO_4$, and 1.0 g/L NaCl), initial RhB concentration (2.5~30.0 mg/L) on RhB and COD degradation and $UV_{254}$ absorbance. Results: Experimental results showed that an increase of applied current in electrolysis reaction with solid polymer electrolyte has resulted in the increase of RhB and $UV_{254}$ degradation. Performance for RhB degradation by electrolyte type was best with NaCl 0.2 N followed by SPE, and $Na_2SO_4$. However, the decrease of $UV_{254}$ absorbance of RhB was different from RhB degradation: SPE > NaCl 0.2 N > $Na_2SO_4$. RhB and $UV_{254}$ absorbance decreased linearly with time regardless of the initial concentration. The initial RhB and COD degradation in electrolysis reaction using SPE showed a pseudo-first order kinetics and rate constants were 0.0617 ($R^2=0.9843$) and 0.0216 ($R^2=0.9776$), respectively. Conclusions: Degradation of RhB in the electrochemical reactor with SPE can be achieved applying electrochemical oxidation. Supporting electrolyte has no positive effect on the final $UV_{254}$ absorbance and COD degradation. Mineralization of COD may take a relatively longer time than that of the RhB degradation.

Terahertz Spectral Characteristics of Electrolyte Solutions under Different Magnetic Fields

  • Shao, Siyu;Huang, Haiyun;Peng, Bo;Wang, Guoyang;Ye, Ping;Wang, Jiahui;Su, Bo;Cui, Hailin;Zhang, Cunlin
    • Current Optics and Photonics
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    • 제6권3호
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    • pp.337-343
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    • 2022
  • Microfluidic chips are new devices that can manipulate liquids at the micrometer level, and terahertz (THz) time-domain spectroscopy has good applicability in biochemical detection. The combination of these two technologies can shorten the distance between sample and THz wave, reduce THz wave absorption by water, and more effectively analyze the kinetics of biochemical reactions in aqueous solutions. This study investigates the effects of different external magnetic field intensities on the THz transmission characteristics of deionized water, CuSO4, CuCl2, (CH3COO)2Cu, Na2SO4, NaCl, and CH3COONa; the THz spectral intensity of the sample solutions decrease with increasing intensity of the applied magnetic field. Analysis shows that the magnetic field leads to a change in the dipole moment of water molecules in water and electrolyte solutions, which enhances not only the hydrogen-bond networking ability of water but also the hydration around ions in electrolyte solutions, increasing the number of hydrogen bonds. Increasing the intensity of this magnetic field further promotes the hydrogen-bond association between water molecules, weakening the THz transmission intensity of the solution.

L-Valine/전해질 및 L-Proline/전해질 수용액에서 아미노산의 활동도계수와 용해도의 측정 및 모델링 (Modeling and Measurements of the Activity Coefficients and Solubilities of Amino Acids in the L-valine/electrolyte and L-proline/electrolyte Aqueous Solutions)

  • 이봉섭;김기창
    • Korean Chemical Engineering Research
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    • 제50권1호
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    • pp.93-105
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    • 2012
  • 본 연구에서는 무기염인 NaCl, KCl, $NaNO_3$$KNO_3$의 각 전해질과 L형 아미노산인 L-Valine 및 L-Proline이 용해된 아미노산/전해질 수용액에서 L-Valine 및 L-Proline의 활동도계수와 용해도를 298.15 K에서 측정하였다. 아미노산의 활동도계수는 양이온 및 음이온의 선택성 전극간의 기전력을 측정하는 전기화학 법으로 측정하였으며, 용해도는 아미노산의 고체상과 상평형을 이루고 있는 포화용액을 중량 분석하여 측정하였다. 실험적으로 측정된 전해질 및 아미노산의 활동도계수 값을 본 연구의 저자들이 수행한 지난번 연구[Korean Chem. Eng. Res. 48(4), 519(2010)]의 이론적 모델로 검토하였다. 실험을 수행한 8개의 아미노산/전해질 수용액에서 측정된 전해질 및 아미노산의 활동도계수 값은 지난번 연구의 이론적 모델에 잘 적용되는 경향을 보였으며, 또한 측정된 아미노산의 용해도 데이터도 지난번 연구의 이론적 관계로 잘 묘사될 수 있었다.

비수용액 전해질에서 전기도금한 니켈-TiO2 복합 도금층의 표면 및 광분해 특성 연구 (Surface and Photolytic Characteristics of Ni-TiO2 Composite Layer Electro-Plated from Non-Aqueous Electrolyte)

  • 조일국;지창욱;최철영;김영석;김양도
    • 한국표면공학회지
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    • 제41권5호
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    • pp.240-244
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    • 2008
  • Composite plating is a method of co-deposition of plating layer with metallic and/or non-metallic particles to improve the plating layer properties such as high corrosion resistance and photolysis of organic compounds. The properties of nickel-ceramic composite plating are significantly depend on the surface characteristics of co-deposited particles as well as the quantity in electrolyte. In this study, Ni-$TiO_2$ composite coating layer was produced by electrodeposition technique from non-aqueous eletrolyte and its surface characteristics as well as photolytic properties were investigated. The amounts of immobilized $TiO_2$ particles increased with increasing the initial $TiO_2$ particles contents in the bath. Samples electroplated with the current density of $0.5\;A/dm^2$ showed the significantly improved homogeneous $TiO_2$ particles distribution. The corrosion resistance of Ni-$TiO_2$ composite coating layer also improved with increaing the amounts of $TiO_2$ particles. Etched sample showed about 10% increased photolytic rate of organic matter compare to that of the non-etched.

유기화합물 첨가제에 따른 철 기반 양극과 polyoxometalate 음극 기반 수계 레독스 흐름 전지의 성능 관계 (Performance Relationship of Iron-Based Anolyte According to Organic Compound Additives and Polyoxometalate-Based Catholyte in an Aqueous Redox Flow Battery)

  • 이서진;권병완
    • 공업화학
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    • 제35권3호
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    • pp.255-259
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    • 2024
  • 본 연구에서는 음극 활물질로 폴리옥소메탈레이트(polyoxometalate, POM)인 규소텅스텐산(tungstosilic acid, TSA)과 양극 활물질로 염화 철(iron chloride)을 사용하고, 지지 전해질 황산(H2SO4) 수용액을 이용한 수계 레독스 흐름 전지(redox flow battery, RFB)를 구성하였다. 운전 결과에 따르면 용량 저하와 낮은 에너지 효율을 보이는 문제점이 있었다. 이와 같은 문제를 해결하기 위해서 양극 활물질에 유기화합물 첨가제인 말산(malic acid)를 첨가하여, 첨가제에 따른 전기화학적 특성과 셀 충방전 테스트를 진행하였다. 말산은 염화 철 수용액에서 킬레이트제로 작용하였으며, 말산내 두 개의 카르복실기가 철 이온과 효과적으로 배위결합을 형성한다. 이는, 양극 활물질인 염화 철의 전해질 저항을 줄어들게 하여 화학적으로 안정화되어 용량과 에너지 효율의 증가를 이끌어냈다.

A New Method to Measure the Conversion of Radiation Polymerization of Electrolyte Monomer Diallyldimethylammonium Chloride in Dilute Aqueous Solution

  • Zhang, Yalong;Yi, Min;Ren, Jing;Zhai, Maolin;Ha, Hongfei
    • Macromolecular Research
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    • 제11권3호
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    • pp.146-151
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    • 2003
  • The dependence of electrical conductivity on concentrations of diallyldimethylammonium chloride (DADMAC) monomer, linear poly(DADMAC) and their mixture monomer/poly(DADMAC) in dilute aqueous solution exhibits a linear relationship. It was possible to calculate conversion of DADMAC polymerization by measuring its electric conductivity. Although the electrical conductivity of the poly(DADMAC) solution decreased with increasing its molecular weight, in the process of UV or ionizing radiation polymerization the molecular weight of the polymers could be kept constant in the case of fixed temperature, UV-luminous intensity or dose rate. Based on the method mentioned above, the kinetics of UV induced polymerization of DADMAC in aqueous solution was studied; the overall activation energy of polymerization of DADMAC in the water phase was calculated to be 18.8 kJ mol$^{-1}$ . ${\gamma}$-Radiation-induced polymerization of DADMAC in aqueous solution as a function of absorbed dose was studied as well. The conversion of DADMAC increased quickly with dose before 30 kGy and then increased slowly. The experimental data of both UV- and ${\gamma}$-induced polymerization were verified to be reliable by inverted ultracentrifugation method.