• Applied Chemistry for Engineering
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• v.21 no.4
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• pp.475-478
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• 2010

Fluorinated polymeric membranes were prepared by direct surface modification of PDMS with fluorine gas ($50{\sim}2000\;{\mu}mol/mol$ in nitrogen). The formed fluorinated polymeric membranes were characterized by FT-IR spectroscopy, GC (Gas chromatography), atomic force microscopy, and scanning electron microscopy. Direct fluorination resulted in the change of permeability and selectivity of various gases (pure gases such as $CO_2$, $O_2$, $N_2$, $C_2H_4$, mixture of He, Ne, Kr, Xe) through PDMS membranes. Fluorination resulted in the maximum 50% increase of selectivity through PDMS membrane.

• Journal of Korean Society of Environmental Engineers
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• v.32 no.7
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• pp.714-721
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• 2010

This research was undertaken to evaluate the feasibility of lanthanum hydroxide for fluoride removal from aqueous solutions. A batch sorption experiments were conducted to study the influence of various factors such as pH, contact time, initial fluoride concentration and temperature on the sorption of fluoride on lanthanum hydroxide. The optimum fluoride removal was observed in the $pH_{eq}{\leq}8.8$. Sorption equilibrium of fluoride on lanthanum hydroxide was better described by the Freundlish isotherm model than by the Langmuir isotherm model. The adsorption energy obtained from D-R model was 9.21 kJ/mol indicating an ion-exchange process as primary adsorption mechanism. The pseudo-second-order kinetic model described well the experimental kinetic data. Thermodynamic parameters such as ${\Delta}Go^{\circ}$, ${\Delta}H^{\circ}$ and ${\Delta}S^{\circ}$ indicated that the nature of fluoride sorption is spontaneous and endothermic. The used lanthanum hydroxide could be regenerated by washing with NaOH solution. Also, the results applied to real ground water indicate that fluoride selectivity and removal capacity of lanthanum hydroxide were superior to those of PA anion-exchange resin.

• Applied Chemistry for Engineering
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• v.10 no.6
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• pp.913-916
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• 1999

Fluorine modified diisocyanate(FMD) was synthesized from tris(6-isocyanatohexyl)isocyanurate(TIHI) and N-ethyl-N-2-hydroxyethyl-perfluorooctanesulfonamide(HFA). Fluorine modified polyurethane(FMPU) was also synthesized from FMD and poly(tetramethylene) glycol(PTMG). Modified polyurethanes were made by blending FMPU into the polyester type base polyurethane(BPU). Surface and thermal properties of the blended BPU film was measured by contact angle measurement and DSC. As the amounts of FMPU was increased from 0 wt % to 1 wt %, the surface energy was dramatically decreased from 47.82 dyne/cm to 17.64 dyne/cm. But we observed little change of the contact angle with further increase in the amount of the FMPU up to 10 wt %. The data meant that the surface of the blended polyurethanes was hydrophobic due to the surface arrangement of the fluorine containing moiety in FMPU. Phase separation was induced by the incompatibility of FMPU and BPU for the samples having over 5 wt % of FMPU. The thermal analysis data of these samples showed the thermal behavior of the FMPU itself.

• Korean Chemical Engineering Research
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• v.46 no.1
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• pp.118-123
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• 2008

In the present study, the effect of oxyfluorination treatment on multi-walled nanotubes (MWNTs) supports was investigated by analyzing surface functional groups. The surface characteristics were determined by Fourier transformed-infrared (FT-IR) and X-ray photoelectron spectroscopy (XPS). After the deposition of platinum nanoparticles on the above treated carbon supports, a crystalline size and a loading level had been investigated. Electrochemical properties of the treated MWNTs-supported Pt (Pt/MWNTs) catalysts were analyzed by current-voltage curve measurements. From the results of surface analysis, an oxygen and fluorine-containing functional group had been introduced to the surface of carbon supports. The oxygen and fluorine contents were the highest value at the treatment of 100 temperature. The Pt/100-MWNTs showed the smallest particle crystalline size of 3.5 nm and the highest loading level of 9.4% at the treatment of 100 temperature. However, the sample treated at the higher temperature showed the larger crystalline size and the lower loading level. This indicated that the crystalline size and the loading level could be controlled by changing the temperature of oxyfluorination treatment. Accordingly, an electrochemical activity was enhanced by increasing the temperature of treatment upto 100, and then decreased in the case of 200 and 300. The highest specific current density of 120 mA/mg had been obtained in the case of Pt/100-MWNTs.

• Proceedings of the Korean Fiber Society Conference
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• 2001.10a
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• pp.265-269
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• 2001

nylon 6의 단점인 저온에서의 연성 및 내충격성 저하를 개선하는 동시에 nylon 6의 내후성도 개선시키는 방법의 하나로 유리전이온도가 매우 낮고, 내가수분해성, 내후성 및 연성(ductile property)이 뛰어난 불소함유 고분자계의 한 종류인 PVDF(polyvinylidene fluoride)를 nylon 6에 용융블렌드 하는 방법이 제안되었다. [1-5] (중략)

• Proceedings of the Korean Institute of Surface Engineering Conference
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• 2012.05a
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• pp.225-226
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• 2012

전기방사법으로 형성한 마이크로 크기의 실리카($SiO_2$) 코팅층 위에 광환원법(photo-reduction mothod)를 이용하여 나노 크기의 금속 나노입자를 형성하여 마이크로-나노 계층구조(hierarchical structure)의 코팅층을 형성하였다. 자외선(UV선) 조사강도 및 조사시간의 변화에 따른 미세구조 및 표면 평활도지수(roughness factor) 변화 거동을 관찰하였고, 이 코팅층에 불소화 처리를 하여 초소수성 표면을 형성하였다.

• Polymer(Korea)
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• v.27 no.3
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• pp.176-182
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• 2003

The fluorine-containing epoxy resin, 2-trifluorotoluene diglycidylether (FER) was prepared by reaction of 2-chloro-${\alpha}$,${\alpha}$,${\alpha}$-trifluorotoluene with glycerol diglycidylether in the presence of pyridine catalyst. Curing behavior of FER/DDM system was investigated using dynamic and isothermal DSC. Cure activation energy (Ea) was determined by Flynn-Wall-Ozawa's equation. The rheological properties of FER/DDM system were studied under isothermal condition using a rheometer. Cross-linking activation energy (Ec) was determined from the Arrhenius equation based on gel time and curing temperature. As a result, the chemical structure of FER was confirmed by FT-IR, $\^$13/C NMR, and $\^$19/F NMR spectroscopy. The cure activation energy of FER/DDM system was 55.4 kJ/mol and conversion and conversion rate were increased with the curing temperature. The cross-linking activation energy of FER/DDM system was 41.6 kJ/mol and gel time was decreased with the curing temperature.

• Journal of the Korean Chemical Society
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• v.45 no.5
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• pp.413-421
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• 2001

The carbon electrodes for fluorine electrolysis were prepared from petroleum cokes containing coal tar pitch as binder and the effects of binder contents on electrode properties were investigated. The evaluations were performed by cyclic voltammogram in the 0.5 M $K_2SO_4$ solution with 1 mM $[Fe$(CN)_6$]^{3-}$/$[Fe$(CN)_6$]^{4-}$redox couple, mechanical strength, and electrochemical behaviour in molten $KF{\cdot}2HF$ electrolyte. It was revealed that the carbon anode formed with 40wt% of coal tar pitch as binder has a better electrode properties compared to those of the other carbon anode, which led to the increase in the effective internal surface area due to proper size and distribution of pores on carbon anode.

• Journal of the Korean Crystal Growth and Crystal Technology
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• v.12 no.1
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• pp.42-49
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• 2002

Differences in electrode properties and in fluorine electrolysis behaviors of various carbon anodes, which were the YBD-like grade carbon, the YBD grade carbon and the P2X grade carbon, containing different pore sizes and distributions were investigated. The evaluations were performed by measuring their mechanical properties, cyclic voltammograms and chronoamperometries in 0.5 M $K_2SO_4$ solution with 1 mM $[[Fe(CN)_6]^\;{3-}/Fe(CN)_6$] $^{4-}$ redox couple and electrochemical behaviours of fluorine electrolysis in molten KF . 2HF electrolyte at $85^{\circ}C$. It was found that the P2X grade carbon anode showed better electrode properties in the cyclic voltammogram and chronoamperometry than the other carbon anodes while the YBD-like grade carbon anode which contained the pore size of 200~300$\mu$m showed superior electrode properties for fluorine electrolysis to the others. These differences in the electrode properties of various carbon anodes seemed to be owing to different sizes and distributions of pores on their surfaces.

• Membrane Journal
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• v.17 no.2
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• pp.81-92
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• 2007

Membrane-based separation processes are receiving increasing attention in the scientific community and industry since they provide a desirable alternative to processes that are not easy to achieve by conventional separation technologies. In particular, gas separation using polymeric membranes have annually grown so fast owing to advantages such as easy installation, no moving parts, small footprint and low energy process. The key element is definitely a polymer membrane exhibiting high permeability and high selectivity to compete with other gas separation technologies. Current polymer membranes used for commercial gas separation are a family of hydrocarbon polymers for hydrogen separation, air separation and carbon dioxide separation from natural gas sweetening. Relatively, gas or vapor separation properties of fluoropolymers are not known so much as compared with those of hydrocarbon polymers. Accordingly, in this study, membranes prepared from amorphous perfluoropolymers are of particular interest because of the unique properties of these polymers. The advantages offered by these amorphous perfluoropolymers for use in gas and vapor separation will be discussed. In addition, membrane properties and separation performance will be compared with other membranes available on the market.