• 멤브레인
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• 제34권2호
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• pp.132-139
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• 2024

Total dissolved solids (TDS) 제거에 이용되는 이온교환수지는 컬럼에 충진시켜 사용하게 되는데, 이온교환 과정에서 이온성 물질과 이온교환수지의 충분한 접촉시간을 필요로 한다. 본 연구에서는 이온교환수지의 분체화를 통하여 짧은 접촉시간으로도 높은 TDS 제거 성능을 보이는 이온교환수지의 특성을 연구하였다. 흐름성 등을 고려한 분체의 최적 크기는 100 ㎛ 이상임을 확인하였고, 250~500 ㎛d와 100~250 ㎛ 크기의 최대 분쇄 수율은 각각 67.3%와 36.9%였다. 또한 100~500 ㎛ 크기의 분쇄 수율은 분쇄 시간 2분에서 87.1%로 나타났다. 회분식(batch) 실험 조건에서 250~500 ㎛ 크기의 분체가 95%와 99%의 제거율에 도달하는 시간은 분쇄 전(non-pulverized) 이온교환수지에 비해 각각 1.82배와 1.96배 더 빨랐다. 100~250 ㎛ 크기의 분체는 각각 15.9배와 6.18배 더 빨랐다. 컬럼 테스트의 경우 분쇄 전 이온교환수지는 총 1.74 g, 250~500 ㎛ 크기의 분체는 1.83 g, 100~250 ㎛ 크기의 분체는 1.63 g의 NaCl을 제거하였다. 분체의 크기가 작아질수록 용량(capacity)이 약간 감소한 것으로 나타났다. 결과적으로 분체화된 이온교환수지를 사용하는 것이 접촉시간 대비 높은 TDS 제거 성능을 얻을 수 있는 방법임을 확인하였다.

• Bulletin of the Korean Chemical Society
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• 제27권5호
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• pp.694-698
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• 2006

A method has been described for the chemical speciation, preconcentration and determination of Cr(III) and Cr(VI) species in filtered tannery waste waters by flame atomic absorption spectrometry using ion-exchange resins. Amberlite IR-120($H^+$) strongly acidic cation exchanger and Amberlite IRA-410($CI ^-$) strongly basic anion exchanger resins were used for the separation and preconcentration of Cr(III) and Cr(VI) species, respectively. Optimum condition for preconcentration and speciation was obtained by testing pH of sample and eluent, flow rates of sample and eluent, amount of resins, volume of sample and eluents, and effect of foreign ions. The recommended method has been successfully applied for the preconcentration and determination of chromium species in the dissolved phase of waste water samples collected from a tannery waste water treatment plant in Kayseri, Turkey. The detection limits achieved were 0.73 $\mu$g/L for Cr(III) and 0.81 $\mu$g/L for Cr(VI). Recovery studies showed 99% for Cr(III) and 98% for Cr(VI), for samples spiked with single species.

• 대한치과보철학회지
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• 제29권3호
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• pp.171-179
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• 1991

The purpose of this study was to investigate the color stability of 3 porcelain repair composite resins Twenty specimens of each composite resin were made and ten specimens were polished at 10 minutes after polymerization, and the others were polished at 48 hours after polymerization. For 60 days, the color characteristics were measured by fiber-optic colorimeter (Model Tc-6FX, Tokyo Denshoku Co.). The obtained results were as follows: 1. The changes of $a^*$ value and $b^*$ value in composite resin polished at 10min. after polymerization were greater than those of composite resins polished at 48 hrs. after polymerization. 2. The $a^*$ values of all composite resins were increased and the $b^*$ values were decreased. 3. The $L^*$ values were decreased in composite resin manufactured by K & B Co., which were polished at 10min. after polymerization, but increased in composite resin manufactured by K & M Co., polished at 48 hrs. after polymerization.

• 대한치과보철학회지
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• 제31권4호
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• pp.523-531
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• 1993

The purpose of this study was to investigate the color change of denture base resins by coffee. Denture base resins for this study were Triad VLG Denture Base (Dentsply, York Div. U.S.A.), Premium Super-20 (Lang Dental Mfg. Co., Inc., U.S.A.) for denture base, Toughron Rebase (Miki Chemical Prod., Kyoto, Japan), Jet Repair Acrylic (Lang Dental Mfg. Co., Inc., U.S.A.), Triad Reline (Dentsply, fork Div. U.S.A.) and Tokuso Rebase (Tokuyama Soda Co., Ltd., Japan) for denture rebase. Twenty specimens of each denture base resin were made and polished. The color of specimens was measured by colorimeter (Model Tc-6FX, Tokyo Denshoku Co. Japan), and they were stored in coffee for three weeks and then color changes were measured. The obtained results were as follows : 1. The L*, a*, b* and the E*ab values of all denture base resins were changed after three weeks. 2. The amount of color change on L*, a*, b* and the E*ab value of each specimens showed different patterns. 3. The b* values of Triad Reline materials were changed more than the other materials. 4. The E*ab values of Triad Denture Base materials were changed more than the other materials.

• 한국염색가공학회지
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• 제20권6호
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• pp.87-91
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• 2008

It is commonly known that water repellency of the fabric treated with fluorocarbon resin brings about a decrease by the washing and recovers by the subsequent heat treatment. In this article, effect of the water repellency was investigated on the nylon 6, triacetate and silk fabrics treated with hydrocarbon and silicon resins. Hydrocarbon and silicon resins have been widely used in the textile finishing as the softening and water proofing agents. The fabrics were treated with hydrocarbon resins, Paragium JQ and RC (Ohara Paragium Chemical Co.) and a silicon resin, Poron MR (Shinetsu Chemical Co.), and then washed and subsequently heat treated. Although the water repellency increased by the resin treatment, it decreased by the washing apparently and recovered a little by the heat treatment. The effect of the heat treatment was small comparing with that of the fluorocarbon resin. Furthermore, as a mechanical property of the treated fabric, KES shearing and bending hysteresis parameters, modulus and hysteresis width of the hydrocarbon resin-treated nylon 6, triacetate and silk fabrics decreased by the heat treatment after washing. Therefore, the treatment is effective at improving the softening of the fabric in water repellent finish.

• 한국응용과학기술학회지
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• 제23권1호
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• pp.85-91
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• 2006

Acrylic resins (HSCs : EA/EMA/2-HEMA/CLA) which contain 80% solid content were synthesized by the copolymerization of monomers (ethyl acrylate, ethyl methacrylate, 2-hydroxyethyl methacrylate) and functional monomer (caprolactone acrylate : CLA) which improves the crosslinking density and physical properties of films. The physical properties of the prepared acrylic resins (HSCs) containing CLA, are as follows: viscosity 1440$^{\sim}$2630 cps ; $M_n$ 1590$^{\sim}$1660 ; and conversions, 81$^{\sim}$86%, respectively. From the correlation of $T_g$ values, viscosities, and $M_n$ of the HSCs, it was found thst viscosity and $M_n$ increased with $T_g$ value.

• 한국응용과학기술학회지
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• 제21권3호
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• pp.197-203
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• 2004

Acrylic resins ($HSC_s$ : EA/EMA/2-HEMA/CLA) which contain 70% solid content were synthesized by the copolymerization of monomers (2-hydroxyethyl methacrylate, ethyl acrylate, and ethyl methacrylate) and functional monomer (caprolactone acrylate : CLA) which improves the crosslinking density and physical properties of films. The physical properties of the prepared acrylic resins (HSCs) containing CLA, are as follows : viscosity 245${\sim}$515 cps ; $M_n$ 2670${\sim}$2840 ; and conversions, 83${\sim}$91%, respectively. From the correlation of $T_g$ values, viscosities, and $M_n$ of the HSCs, it was found that viscosity and $M_n$ increased with $T_g$ value.

• 한국소성가공학회:학술대회논문집
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• 한국소성가공학회 2004년도 춘계학술대회 논문집
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• pp.159-165
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• 2004

The shrinkages of injection molded parts are different in molding operational conditions and mold design. It also differs from resins. The shrinkages of injection molded parts for PBT (polybutylene terephthalate), PC (polycarbonate),and glass reinforced PBT and PC have been studied for various operational conditions of injection molding. The part shrinkage of crystalline polymer, PBT was higher than that of amorphous polymer, PC by about two times. The part shrinkages of both polymers decreased as glass fiber content increases. Higher Injection temperature and lower injection pressure resulted in a higher shrinkage in both PBT and PC resins. As mold temperature increases the part shrinkage of PC decreased. However, the part shrinkage of PBT increased as mold temperature increases. The part shrinkage of both PBT and PC resins decreased as gate size increases since the pressure delivery is mush easier for a larger gate size. The part shrinkage of flow direction was less than that of the perpendicular direction to the flow for both pure and glass fiber reinforced resins. The part shrinkage at the position close to the gate was less than that of the position far from the gate.

• 한국소성가공학회:학술대회논문집
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• 한국소성가공학회 2004년도 제5회 압연심포지엄 신 시장 개척을 위한 압연기술
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• pp.249-257
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• 2004

Drying and curing characteristics of PCM resins using the induction heater and short-wave infrared emitter module was studied to develop a compact oven system for the high speed CCL and post-treatment equipment. Drying of the polyester resins using the induction heater and infrared heater showed that the blistering tendency of polyester resin coating increased regardless of additives and colors of resins as the heating rate and/or dry film thickness increased. The blistering of polyester resin coating layer occurred when the heating speed was over than $25^{\circ}C/sec$ for the dry film thickness of $19\~20um$, which is the typical thickness of finish coating in CCL. So did it when the heating speed was over than $40^{\circ}C/sec$ for the dry film thickness over than 10 um. The heating efficiency of paint coated steels by the infrared heating was strongly dependent on the colors of paint coating and generally increased for the dark surface and/or coating. But the faster drying of the PCM resin coatings increased the blistering tendency of coating layer. The blistering limit for the typical finish coating by the infrared heating was estimated as the heating rate slower than $20^{\circ}C/sec$ regardless of colors of PCM resins.

• 분석과학
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• 제8권3호
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• pp.397-404
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• 1995

Three Arsenazo I-XAD Chelating resins, with different surface areas and pore sizes were synthesized and characterized. The total sorption capacities of these chelating resins for Cu(II) at pH 5.0 by batch method decreased as follows, Arsenazo I-XAD-16(0.59mmol/g)>Arsenazo I-XAD-4(0.56mmol/g)>Arsenazo I-XAD-2(0.38mmol/g). The sorption and desorption properties of Arsenazo I-XAD-16 chelating resins for U(VI), Th(IV), Hf(IV), Zr(IV), Ni(II), Mn(II), Cd(II). and Cu(II) were studied by both batch and elution method. The Arsenazo I-XAD-16 chelating resin was successfully applied to the separation and concentration of trace U(VI) and Th(IV) in sea and waste waters.