• 한국염색가공학회지
• /
• 제3권3호
• /
• pp.15-22
• /
• 1991

The effects of electrolytes on color fastness properties of cotton fabric with Congo Red have been studied at $90^{\circ}C$. Each dyeing carried with $10 \times 10^{-6}M$ of Congo Red and with various concentration of electrolytes. The results obtained from this study were as follow 1. In the case of none, the fastness to washing became worse, but the fastness to light better with increasing dye concentration. 2. In the case of additing an electrolyte, the fastness to washing became worse and the fastness to light better than the case of none. The samples had become yellower after washing test. Yellowness had been reduced after fade-O-meter test. 3. What kind of electrolytes could not have any effect on the fastness to washing, but they influenced the fastness to light in the order of LiCl

• Fibers and Polymers
• /
• 제7권2호
• /
• pp.89-94
• /
• 2006

Ionic conductivity and mechanical properties of a mixed polymer matrix consisting of poly(ethylene glycol) (PEG) and cyanoresin type M (CRM) with various lithium salts and plasticizer were examined. The CRM used was a copolymer of cyanoethyl pullulan and cyanoethyl poly(vinyl alcohol) with a molar ratio of 1:1, mixed plasticizer was ethylene carbonate (EC) and propylene carbonate (PC) at a volume ratio of 1:1. The conductive behavior of polymer electrolytes in the temperature range of $298{\sim}338\;K$ was investigated. The $PEG/LiClO_4$ complexes exhibited the highest ionic conductivity of ${\sim}10^{-5}S/cm$ at $25^{\circ}C$ with the salt concentration of 1.5 M. In addition, the plasticized $PEG/LiClO_4$ complexes exhibited improvement of ionic conductivity. However, their complexes showed decreased mechanical properties. The improvement of ionic conductivity and mechanical properties could be obtained from the polymer electrolytes by using CRM. The highest ionic conductivity of PEG/CRM/$LiClO_4$/(EC-PC) was $5.33{\time}10^{-4}S/cm$ at $25^{\circ}C$.

• 한국세라믹학회지
• /
• 제51권4호
• /
• pp.260-264
• /
• 2014

We developed a novel double dopant bismuth oxide system with Tb and W. When Tb was doped as a single dopant, a Tb dopant concentration more than 20 mol% was required to stabilize bismuth oxides with a high conductivity cubic structure. High temperature XRD analysis of 25 mol% Tb-doped bismuth oxide (25TSB) confirmed that the cubic structure of 25TSB was retained from room temperature to $700^{\circ}C$ with increase in the lattice parameter. On the other hand, we achieved the stabilization of high temperature cubic phase with a total dopant concentration as low as ~12 mol% with 8 mol% Tb and 4 mol% W double dopants (8T4WSB). Moreover, the measured ionic conductivity of 10T5WSB was much higher than 25TSB, thus demonstrating the feasibility of the double dopant strategy to develop stabilized bismuth oxide systems with higher oxygen ion conductivity for the application of SOFC electrolytes at reduced temperature. In addition, we investigated the long-term stability of TSB and TWSB electrolytes.

• 한국재료학회지
• /
• 제18권6호
• /
• pp.334-338
• /
• 2008

The purpose of this study is to characterize various electrolytes on electrochemical mechanical planarization (ECMP). The ECMP system was modified from conventional CMP system to measure the potentiodynamic curve and removal rate of Cu. The potentiodynamic curves were measured in static and dynamic states in investigated electrolytes using a potentiostat for the evaluation of the polishing behavior on ECMP. KOH (alkaline) and $NaNO_3$ (salt) were selected as electrolytes which have high conductivity. In static and dynamic states, the corrosion potential decreased and the corrosion current increased as a function of the electrolyte concentration. But, the electrochemical reaction was prevented by mechanical polishing effect in the dynamic state. The static etch and removal rate were measured as functions of concentration and applied voltage. When $NaNO_3$ was used, the dissolution was much faster than that of KOH. It was concluded that the removal rate was strongly depended on electrochemical dissolution. The removal rate increased up to 350 nm/min in $NaNO_3$ based electrolyte.

• Bulletin of the Korean Chemical Society
• /
• 제35권2호
• /
• pp.466-470
• /
• 2014

In this paper, organic solvent electrolytes were prepared by a mixture of propylene carbonate (PC), dimethyl carbonate (DMC), tetraethylammonium tetrafluoroborate ($TEABF_4$)s to evaluate the ionic properties of propylene carbonate (PC)/dimethyl carbonate (DMC) mixtures as solvents for a capacitor application, in view of improving the electrochemical performances. The bulk resistance and interfacial resistance of the mixture electrolytes were investigated using an AC impedance method. The morphology of carbon-based electrodes which were contained in different electrolytes was analyzed by scanning electron microscopy (SEM) method. From the experimental results, by increasing the FEC content, capacitance of electrodes was increased, and the interfacial resistance was decreased. In particular, by a content of 2 vol % FEC in 0.2 M $TEABF_4$ PC/DMC solvent, the electrolyte showed the superior capacitance. However, when FEC content exceeds 2 vol %, the capacitance was decreased and the interfacial resistance was increased.

• 폴리머
• /
• 제32권1호
• /
• pp.85-89
• /
• 2008

이온성 액체인 N-methoxymethyl-N-methylpyrrolidium bis(trifluoro-methansulfonyl)imide (MPSI)를 첨가제로 함유하는 acrylate 계열의 단량체를 다관능기형 acrylate 가교제와 함께 carbonate 용매에서 중합, 겔형의 고분자 전해질을 합성하였다. 고분자 전해질의 이온전도성은 고분자의 함량, 가교제의 종류, 이온성 액체의 함량에 따라 측정되었으며, 인장강도를 조사하여 고분자 및 이온성 액체의 함량이 기계적 물성에 미치는 영향을 파악하였다. 그 결과 성분의 최적화는 고분자 함량 15 wt%, 이온성액체 30 wt% 그리고 5 wt%의 가교제를 함유한 겔 전해액으로 달성되었고, 0.5 MPa의 기계적 물성과 0.8 mS/cm의 우수한 상온 이온 전도도를 나타내었다.

• 전기화학회지
• /
• 제13권2호
• /
• pp.110-115
• /
• 2010

The plasticized polymer electrolytes based on polyvinylidene fluoride-co-hexafluoropropylene (P(VdF-co-HFP)), tetra (ethylene glycol) dimethyl ether (TEGDME), and lithium perchlorate ($LiClO_4$) are prepared for the lithium sulfur batteries by solution casting with a doctor-blade. The polymer electrolyte with EO : Li ratio of 16 : 1 shows the maximum ionic conductivity, $6.5\;{\times}\;10^{-4}\;S/cm$ at room temperature. To understand the effect of the salt concentration on the electrochemical performance, the polymer electrolytes are characterized using electrochemical impedance spectroscopy (EIS), infrared spectroscopy (IR), viscometer, and differential scanning calorimeter (DSC). The optimum concentration and mobility of the charge carriers could lead to enhance the utilization of sulfur active materials and the cyclability of the Li/S unit cell.

• Bulletin of the Korean Chemical Society
• /
• 제27권1호
• /
• pp.82-86
• /
• 2006

Propylene Carbonate (PC) has the interesting properties of being able to dissolve and dissociate lithium salts, thus leading to highly conducting electrolytes even at low temperatures. Moreover, electrolytes that contain PC are stable against oxidation at voltages up to ~5 V. However, it is known that, when lithium is intercalated into graphite in pure PC based electrolytes, solvent co-intercalation occurs, leading to the destruction of the graphite structure. (i.e., exfoliation). The objective of this study was to suppress PC decomposition and prevent exfoliation of the graphite anode by co-intercalation. Electrochemical characteristics were studied using Kawasaki mesophase fine carbon (KMFC) in different 1 M $LiPF_6$/PC-based electrolytes. Electrochemical experiments were completed using chronopotentiometry, cyclic voltammetry, impedance spectroscopy, X-ray diffraction, and scanning electron microscopy. From the observed results, we conclude that the MA and $Li_2CO_3$ additive suppressed co-intercalation of the PC electrolyte into the graphite anode. The use of additives, for reducing the extent of solvent decomposition before exfoliation of the graphite anode, could therefore enhance the stability of a KMFC electrode.

• 한국응용과학기술학회지
• /
• 제8권2호
• /
• pp.153-159
• /
• 1991

The electrochemical oxidation of p-methoxyphenol and hydroquinone for wastewater treatment application was investigated on platinum anode. At the cyclic voltammetry, it was observed that nagative shift of peak potential of p-methoxyphenol and hydroqinone as the pH of electrolytes increases and the peak current showed higher at strong electrolytes than weak electrolytes. In the case of p-methoxyphenol, the optimum electrode potential of controlled potential electrolysis was observed at the potential region of 0.8-1.0 (V vs. SCE) and hydroquinone was showed at the potential of l.0(V vs. SCE). Specially the oxidation rate of p-methoxyphenol and hydroquinone was showed high value in the acid electrolytes.

• Macromolecular Research
• /
• 제16권3호
• /
• pp.247-252
• /
• 2008

Lithium gel electrolytes based on a mixed polymer matrix consisting of poly(vinylidenefluoride-hexafluoropropylene) (PVDF-HFP) and cyanoresin type M (CRM) were prepared using an in situ blending process. The CRM used in this study was a copolymer of cyanoethyl pullulan and cyanoethyl poly(vinyl alcohol) (PVA) with a mole ratio of 1:1. The mixed plasticizer was ethylene carbonate (EC) and propylene carbonate (PC) with a volume ratio of 1:1. In this study, the presence of PVDF in the electrolytes helps to form a dimensionally stable film over a broad composition range, and decreases the viscosity. In addition, it provides better rheological properties that are suitable for the extrusion of thin films. However, the presence of HFP has a positive effect on generating an amorphous domain in a crystalline PVDF structure. The ionic conductivity of the polymer electrolytes was investigated in the range 298-333 K. The introduction of CRM into the PVDF-HFP/$LiPF_6$, complex produced a PVDF-HFP/CRM/$LiPF_6$ complex with a higher ionic conductivity and improved thermal stability and dynamic mechanical properties than a simple PVDF-HFP/$LiPF_6$, complex.