• 한국지하수토양환경학회:학술대회논문집
• /
• 한국지하수토양환경학회 1998년도 공동 심포지엄 및 추계학술발표회
• /
• pp.236-239
• /
• 1998

This research was performed to check the transport characteristics of heavy metals in contaminated soil, that is, the influence of humic acid and phosphate on transport characteristics of heavy metals was studied. From the results of column mode experiments about heavy metal behavior, the order time to reach breakthrough and equilibrium was soil ＋ humic acid( 20g ) > soil ＋ humic acid ( 5 g ) > soil without Humic acid addition > soil+humic acid( 50g ). It is because the dissolved organic carbon content increased as the soil organic matter content increased. As the phosphate increased, so did the time to reach breakthrough and equilibrium. The order of time was soil + phosphate( 50 mg ) > soil + phosphate( 20 mg ) > soil . phosphate( 10 mg ) > soil without phosphate addition. It is because the phosphate ion worked as alkalinity donor and the calcium ion co-injected worked as the accelerator of coprecipitation of heavy metals.

• 분석과학
• /
• 제5권4호
• /
• pp.425-431
• /
• 1992

$La(OH)_3$ 공침에 의한 극미량 인산이온의 부선 및 농축에 관한 연구를 가시/자외선 분광광도법을 이용하여 수행하였다. 암모니아용액으로 조절한 pH 9.5의 1.0L 시료용액 중 인산 이온을 수산화란탄 침전에 공침시켰다. 1:8의 sodium oleate와 sodium dodecyl sulfate 혼합 계면활성제를 가하고 질소기체를 bubbling하여 침전들을 용액 표면으로 띄웠다. 뜬 침전들을 감압 플라스크에 모은 다음 용액을 걸러 버리고 침전을 묽은 암보니아용액으로 씻고 황산에 녹였다. 몰리브덴 청색법으로 농축된 용액 중 인산이온을 정량하였다. 이상의 방법으로 수도물과 강물 중 인산이온을 분석하였고 각 시료에 인산이온을 20.0ng/mL 가하여 분석한 결과 각각 93%와 86%의 회수율을 얻었다.

• 분석과학
• /
• 제8권4호
• /
• pp.843-848
• /
• 1995

A sensitive method for the determination of trace amounts of phosphate by fluorescence-quenching detection / FIA is proposed. The fluorescence of Rhodamine B(RB) was quenched with the formation of the ion associate of molybdophosphate with RB;${\lambda}_{ex}$ and ${\lambda}_{em}$ were 560nm and 580nm, respectively. A calibration graph was linear over the ranges from $10^{-8}$ to $3{\times}10^{-6}M$ of phosphate (~0.3~93ppb of phosphorus). The relative standard deviation was 1.2% with $8{\times}10^{-7}M$ phosphate solution and sampling rate was 15 samples / h. The proposed method was applied to the determination of phosphate in sea and river water samples.

• 한국세라믹학회지
• /
• 제36권4호
• /
• pp.380-390
• /
• 1999

• 상하수도학회지
• /
• 제23권1호
• /
• pp.113-119
• /
• 2009

The feasibility of using cork oak bark for phosphorus removal from wastewater was evaluated in this study. Recently, development of more cost-effective media while maintaining high efficiency in pollutants removal has received concern. Barks have a negative surface charge and, hence, tend to show a high affinity to bind cations, and they need to undergo chemical modification to increase their adsorption capacity of anions. Bark was hydrolyzed by HCl solution and it received modification using an aqueous solution of high molecular weight polyethylenimine(PEI). Surface modification with HCl and PEI resulted in a decrease of specific surface area of the bark from $1.932 m^2/g$ to $1.094 m^2/g$. The adsorption experiments were carried out in batch tests and the data were fitted to the Langmuir isotherm and Freundlich isotherm equations. Phosphate removal rate was higher at the lower solution pH possibly due to the form of phosphate ion in solution. For the initial phosphate concentration of 10 mg/L, maximum adsorption was 20.88 mg P/g at pH 3 and 12.02 mg P/g at pH 5. Mechanism of phosphorus sorption onto the HCl-PEI bark was examined through FT-IR spectrometer. Ion exchange between $NH^+$ and $H_2PO_4{^-}$ appeared to be a key mechanism of phosphate adsorption onto the HCl-PEI bark surface.

• Korean Chemical Engineering Research
• /
• 제57권3호
• /
• pp.438-443
• /
• 2019

본 연구에서는 HT-PEMFC 공기극용 Pt계열 연료극 촉매의 인산이온 피독 특성에 대한 새로운 평가 방법을 제시하였다. 이를 위하여, 기존의 전기화학적 인산이온 피독 측정법인 CV와 ORR RDE 측정법이 갖고 있는 문제점을 저감하기 위하여, 과산화수소를 Pt 촉매와의 반응물로 이용하여 고농도 인산 이온 분위기에서의 내피독성 측정값 오차를 감소시켰다. 그 결과 인산이온 농도 0.1 M 이하의 저농도와 0.5 M 이상의 고농도에서 인산농도 대비 전류밀도의 변화가 직선적으로 나타나, 실제 HT-PEMFC의 구동 환경과 유사한 고농도의 인산이온 분위기에서의 Pt계 인산이온 피독 정량화에 대하여 기존의 측정방법에 비해 우수함을 확인하였다.

• 대한치과보철학회지
• /
• 제45권6호
• /
• pp.795-804
• /
• 2007

Statement of problem. Nano-scale calcium-phosphate coating on the anodizing titanium surface using ion beam-assisted deposition (IBAD) has been recently introduced to improve the early osseointegration. However, not much is known about their surface characteristics that have influence on tissue-implant interaction. Purpose. This study was aimed to investigate microtopography, surface roughness, surface composition, and wettability of the titanium surface modified by the anodic oxidation and calcium phosphate coating using IBAD. Material and methods. Commercially pure titanium disks were used as substrates. The experiment was composed of four groups. Group MA surfaces represented machined surface. Group AN was anodized surface. Group CaP/AN was anodic oxidized and calcium phosphate coated surfaces. Group SLA surfaces were sandblasted and acid etched surfaces. The prepared titanium discs were examined as follows. The surface morphology of the discs was examined using SEM. The surface roughness was measured by a confocal laser scanning microscope. Phase components were analyzed using thin-film x-ray diffraction. Wettability analyses were performed by contact angle measurement with distilled water, formamide, bromonaphtalene and surface free energy calculation. Results. (1) The four groups showed specific microtopography respectively. Anodized and calcium phosphate coated specimens showed multiple micropores and tiny homogeneously distributed crystalline particles. (2) The order of surface roughness values were, from the lowest to the highest, machined group, anodized group, anodized and calcium phosphate deposited group, and sandblasted and acid etched group. (3) Anodized and calcium phosphate deposited group was found to have titanium and titanium anatase oxides and exhibited calcium phosphorous crystalline structures. (4) Surface wettability was increased in the order of calcium phosphate deposited group, machined group, anodized group, sandblasted and acid etched group. Conclusion. After ion beam-assisted deposition on anodized titanium, the microporous structure remained on the surface and many small calcium phosphorous crystals were formed on the porous surface. Nanoscale calcium phosphorous deposition induced roughness on the microporous surface but hydrophobicity was increased.

• 한국세라믹학회지
• /
• 제32권10호
• /
• pp.1093-1102
• /
• 1995

Water-soluble phosphate glasses containing Ag or Cu ion were prepared through melting process. Then the powdered glass samples were dissolved in D.I. water at room temperature with changing the dissolution time. In terms with the glass composition, dissolution characteristics, bactericidal effects and cytotoxicities were investigated. Dissolved amounts increased uniformly with dissolution time, and the dissolution rate was higher for ternary glass than for binary glass and with less metal oxide amount. And the dissolution rate of the glass with Ag ion was higher than that with Cu ion, and the bactericidal effect of the glass with Ag ion was also greater. Solution with more than 25 ppm of Ag was observed to have strong cytotoxicity to L929, and solutions of lower Ag concentration or with Cu seemed to have little cytotoxicity.

• 한국환경농학회지
• /
• 제26권4호
• /
• pp.286-296
• /
• 2007

To increase phosphate (P) availability in soils, the efficiency of silicate (Si) in reducing P adsorption was investigated by competitive adsorption tests under changing conditions of pH, ion concentrations, and order of anion addition along with single adsorption properties of each ion at $20^{\circ}C$. In the single ion adsorption study, P and Si ions showed the opposite reaction patterns: phosphate adsorption decreased with increasing pH and attained adsorption maximum however, silicate adsorption increased with increasing pH without attaining adsorption maximum. Phosphorus and Si adsorption were influenced by pH in the range of 5.0 - 9.0 and the type and amount of P and Si concentration. Silicate added to soil before P or in a mixture with P significantly reduced P adsorption above pH 7.0; however, there was no significant Si-induced decreased in P adsorption at pH 5.0 when anions were added as mixture. The efficiency of Si in reducing P adsorption increased with increasing Si concentration and pH. The effect of P on Si adsorption was relatively small at pH 5.0 and no effect of P on silicate adsorption was observed at pH 9.0. The presence of Si strongly depressed P adsorption when Si was added before P compared to P and Si added as a mixture. These results suggest that application of Si may decrease P adsorption and increase the availability of P in soils. Furthermore, a Si source would be better to add before P application to enhance the availability of P in soils.

• 한국표면공학회지
• /
• 제28권5호
• /
• pp.289-299
• /
• 1995

The effects of phosphate coating have been studied on physical properties and corrosion resistance of painted aluminum alloy sheet for automobile body. The physical properties (surface roughness, paint adhesion, impact resistance and pencil hardness) and corrosion resistance(cyclic corrosion and filiform corrosion) were investigated. Phosphate coatings enhanced the physical properties of painted Al alloy sheet, especially paint adhesion after the 240hours water immersion test. Phosphate coating also markedly improved the resistance for cyclic corrosion and filiform corrosion of painted cold rolled steel and Zn-Ni plated steel sheet as well as painted Al alloy sheet. The corrosion resistance of painted Al sheets was varied with the concentration of free fluoride ion and metal additives like Ni and Mn in the phosphating bath. A maximum corrosion resistance was obtained at about 300ppm of fluoride ion and additives of Ni and Mn obviously increased the corrosion resistance of painted specimens.