• 지질공학
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• 제21권3호
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• pp.231-237
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• 2011

현재 고로폐광산에서 가동 중인 인회석 배수체계의 설계는 다음과 같다 ; 인회석 배수시스템은 침사조, 반응조 및 침전조로 구성되며 폐갱도 및 광미장의 침출수를 배관을 통하여 집수한 후 인회석 배수시스템으로 수리구배에 의해 운반되게 설계되었다. 2004년도에 실시된 실내실험 결과에 의하면, 인회석 38.8 톤을 매년 반응조에 새로 충진시켜 줘야 하며 침전물은 매 3개월 마다 침전조에서 제거해줘야 한다. 본 연구의 목적은 석회석 및 인회석을 이용한 실내실험을 실시하여 ARD 내의 비소저감 효율성을 평가하고 침출수 처리 체계 내에 사용되는 침전제를 재평가하는 것이다. 실내실험 결과, 석회석 및 인회석의 비소 저감율은 64.7-98.3%이며 인회석의 경우 비소 저감율은 입도에 반비례하였다. 비소화합물은 비산염인회석 그리고 칼슘비산염수화물의 형태인 것으로 추측된다. 따라서, 인회석 및 인이 포함된 석회석은 저 농도의 비소제거를 위한 침전제로 사용될 수 있는 것으로 판단된다.

• 한국지하수토양환경학회지:지하수토양환경
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• 제9권2호
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• pp.1-10
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• 2004

본 연구의 목적은 석회석 및 인회석을 이용한 실내실험을 실시하여 ARD 내의 비소저감 효율성을 평가하고 인회석 배수 체계를 설계하는 것이다. 실내실험 결과, pH, 비소저감율 및 석회석/인회석의 용해량은 유속에 반비례 하였으며 인회석은 유속 0.6 ml/min/kg에서 비소를 100％ 제거하였다. 인회석의 용해율은 석회석보다 10배 정도 높은 것으로 사료된다. 비소화합물은 비산염인회석 그리고/또는 칼슘비산염수화물의 형태인 것으로 추측된다. 실내실험에 근거하여 인회석 배수체계를 설계하였으며 그 결과는 다음과 같다; 1년 6개월 마다 인회석 62톤을 새로 충진시켜줘야 하며 침전물은 매 3개월 마다 침전조에서 제거해줘야 할 것이다.

• 한국세라믹학회지
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• 제45권10호
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• pp.638-643
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• 2008

Biomimetic apatite formation and deposition behaviors of Ti-6Al-7Nb and Ti-6Al-4V plates in simulated body fluids(SBF) under various conditions were examined. In case of regular samples without collagen treatments the weight gain due to apatite precipitation on the surface in Ti-6Al-4V was found to be higher than in Ti-6Al-7Nb. In case of collagen-coated samples, the weight gain in Ti-6Al-4V continued to be higher than in Ti-6Al-7Nb, but the difference between the two became smaller. Both Ti-6Al-7Nb and Ti-6Al-4V samples with collagen coating exhibited an appreciable increase of weight gain, which may be caused by the interaction between collagen and $Ca^{+2}$ ions. The weight gain was found to be not much affected by the addition of collagen to SBF. The ill-defined granular structure in the presence of collagen can be associated with the increasing volume fraction of amorphous calcium phosphate.

• 자원환경지질
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• 제34권6호
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• pp.617-625
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• 2001

Skaergaard 암체는 광범한 in situ 화성분화작용을 격은 층상관입암의 대표적인 예로 널리 알려져 있다. 따라서 이 암체는 폐쇄계에서 미량원소변이를 modeling 할 수 있는 적지가 될 것이다. 그러나, 기존의 연구에 의하면 본 암체의 전암 및 광물의 회토류는 폐쇄계로서의 예상된 경향을 보이지 않는다(Haskin and Haskin, 1968; Paster et al., 1974). 발표된 분배계수, 공존광물들의 mode,그리고 전암 및 광물의 미량원소함량을 사용한 미량원소modeling에 의하면 Skaergaard 암체의 희토류는 분화후기에 일어난 광범한 인회석 결정작용에 크게 영향을 받았음을 보여준다. 미량원소modeling은 Upper Border Series에서 간헐적으로 나타나는 인회석이 기존에 주장되어 온 바와 같은 liquldus상이 아니라 진화하는 magma의 미량원소함량에는 영향을 끼칠 수 없는 interstitial phase임을 시사한다. 분화작용 말기에 Skaerganrd 마그마가 대류를 멈추거나 소규모로 대류를 할 때, 마그마 암장의 상부에 축적되는 휘발성분에 기인한 증가된 $PH_2$O가 인회석이 UBS에서 정출 되는 것을 방해하였을 것이다. 이와 같은 인회석의 특성을 고려해서 Skaergaard분화작용을 modeling하면 희토류는 폐쇄계로서의 예상된 경향을 따른다 이와 같은 결과는 최종 20% 분화작용기간 중에 양적으로 상당한 양의 마그마의 주입이나 분출을 수반하는 그 어떤 Skaergaard 암체의 분화model도 배격한다.

• 대한치과기공학회지
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• 제21권1호
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• pp.5-14
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• 1999

Glass ceramics for dental crown prosthesis were prepared by crystallization of CaO-MgO-SiO2-$P_2O_5-TiO_2$ glasses. Their crystallization behaviors have been investigated as a function of heattreatment temperature, holding time and chemical composition in relation to mechinical properties. Crystallization peak temperatures were determined by differential thermal analysis(DTA). Crystalline phases and mircostructures of heat-treated sample were determined by the means of powder X-ray diffraction(XRD) and scanning electron microscopy(SEM). The final crystalline phase assemblages and the microstructures of the samples were found to be dependent on glass compositions, heattreatment temperature, and holding time. 1st crystallization peak temperature(TP), affected strongly by apatite, was found to be increased or decreased. From the experiment, the following results were obtained : 1. The crystallization peak temperature($T_P$) formed by apatite increased until adding up to 9wt% $TiO_2$ to base glass composition, then decreased above that. 2. Apatite($Ca_{10}P_6O_{25}$), whitlockite(${\beta}-3CaO-P_2O_5$), $\beta$-wollastonite($CaSiO_3$), magnesium tianate($MaTiO_3$) and diopside(CaO-MgO-$2SiO_2$) crystal phase were precipitated in MgO-CaO-$SiO_2-TiO_2-P_2O_5$ glass system containing 9wt% and 11wt% of $TiO_2$ 3. Vickers hardness of samples increased with increasing heat-treatment temperature and Vickers hardness of S415T9 samples heat-treated at 1075 was approxi-mately 813Kg $mm^{-2}$ as maximum value. 4. Vickers hardness of samples increased due to precipitation of apatite, whitlockite, $\beta$-wollastonite, magnesium titanate, and diopside crystal phases within glass matrix.

• Restorative Dentistry and Endodontics
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• 제20권2호
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• pp.818-826
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• 1995

The present study was undertaken to investigate the crystal growth onto enamel mineral and synthetic hydroxyapatite seeds in media resembling the enamel fluid composition. Effects of fluoride at low concentrations on the precipitation were also examined in a benchtop crystal growth model adopting a miniaturized reaction column. X-ray diffraction and Fourier transform infrared spectroscopy(FTIR), as well as chemical analyses, were employed for characterization of both seed materials before and after experimentation. Remarkable findings were that (1) both biological and synthetic seeds at the same total surface areas yielded rather similar precipitation rates at all levels of fluoride concentration in solution and (2) the precipitation rate was accelerated in a manner depending on fluoride concentrations in media. FTIR differential analysis disclosed that the precipitating phase was characterized as poorly crystallized apatite, which incorporated subtle carbonate. Most of the fluoride ions in soution were readily incorporated into crystals. The overall results support the view that the seeded crystal growth model is of value to gain insight into the mechanism of enamel crystal growth under fluoride regimens.

• 대한소아치과학회지
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• 제25권1호
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• pp.209-224
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• 1998

The purpose of this study was to compare the amount of calcium fluoride deposited on the enamel and dentin surface and to obtain information on the morphological change and crystallographic details of mineral deposition after 12,000ppm APF application in vitro. The bovine enamel and dentin blocks were randomly assigned to eight groups according to artificial caries lesion formation and difference of fluoride application time. The fluoride concentration and morphological characteristics on the treated enamel and dentin surface were investigated by using fluoride quantitative analysis and SEM. The powdered enamel and dentin of the intact bovine incisors were prepared for the X-ray diffraction analysis. The following results were obtained. 1. The amounts of KOH-soluble fluoride on the carious enamel and dentin surface after 24h APF application were higher than after only 5min APF application(p<0.05), but in the case of the sound enamel and dentin surface were similar after 5min and 24h application (P>0.05). The fluoride content was highly increased in the carious dentin as compared with sound dentin after APF application(P<0.05). 2. The carious enamel surface after APF application, the demineralized enamel surface were recovered a more dense enamel surface and precipitation of crystal was observed a distintive surface layer of spherical globules of about 1 m diameter. In the case of the fluorided carious dentin surface, precipitation of calcium fluoride-like material was deposited both inside the dentinal tubules as well as in the intertubular regions. 3. The crystallographic structure of powdered enamel and dentin after 24h APF application had large crystallities of apatite and CaF2 diffraction peaks in the enamel as compared with dentin. The diffraction data collected from the 27.50-29.50(2) angular range of the powdered enamel, the (105) apatite, (225) apatite and (111) CaF2 peaks of the enamel crystallities were detected after 24h APF application.

• 한국환경과학회지
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• 제9권4호
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• pp.325-330
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• 2000

The hydroxyapatite (HAp) for the present study was prepared by precipitation method in semiconductor fabrication and the crystallized at ambient to 95$0^{\circ}C$ for 30min in electric furnace. The ion-exchange characteristics of HAp for various heavy metal ions such as $Cd^{2+}, Cu^{2+}, Mn^{2+}, Zn^{2+}, Fe^{2+}, Pb^{2+}, Al^{3+}, and Cr^{6+}$ in aqueous solution has been investigated. The removal ratio of various metal ions for HAp were investigated with regard to reaction time, concentration of standard solution, amount of HAp and pH of solution. The order of the ions exchanged amount was as follws: $Pb^{2+}, Fe^{3+}>Cu^{2+}>Zn^{2+}>Al^{3+}>Cd^{2+}>Mn^{2+}>Cr^{6+}. The Pb^{2+}$ ion was readily removed by the Hap, even in the strongly acidic region. The maximum amount of the ion-exchange equilibrium for $Pb^{2+}$ ion was about 45 mg/gram of HAp. The HAp would seem to be possible agent for the removal of heavy metal ions in waste water by recycling of waste sludge in semiconductor fabrication.

• 한국지하수토양환경학회:학술대회논문집
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• 한국지하수토양환경학회 2004년도 총회 및 춘계학술발표회
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• pp.139-142
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• 2004

본 논문은 광산산성배수(AMD)에서 철 및 알루미늄 제거 효과가 입증된 인회석을 이용하여 ARD (Acid Rock Drainage)에서의 비소저감 능력을 알아보고 고품위 석회석과 정화효율을 비교하기 위하여 실내실험을 실시하고 그 결과를 이용 인회석 배수로를 설계하는 것을 연구목적으로 하고 있다. 실험결과, pH, 비소제거율 및 석회석/인회석의 용해량은 유속이 증가함에 따라 감소하는 것으로 나타났으며 유속이 0.6 ml/min/kg 정도에서 인회석은 침출수 중 비소를 100% 제거하는 것으로 확인되었다. 유속에 따른 용해율은 인회석이 석회석보다 10배 정도 높은 것으로 나타났다.

• 대한의용생체공학회:학술대회논문집
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• 대한의용생체공학회 1998년도 추계학술대회
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• pp.231-232
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• 1998

The purpose of this study was to examine whether the precipitation of calcium phosphate on titanium surface was affected by surface modification. To improve the bone conductivity, of titanium, samples were devided into 4 groups. Group 1 was immersed in 5M-NaOH solution at $60^{\circ}C$ for 24 hours. Group 2 was immersed in 5M-NaOH solution at $60^{\circ}C $ for 24 hours and heat-treated at $600^{\circ}C$ for 1 hour. Group 3 was anodized in Hanks' solution at 1V, $25^{\circ}C$ for 1 hour. Group 4 was anodized in Hanks' solution at 5V, $80^{\circ}C$ for 5 minutes. And then, all specimens were immersed in the MEM Eagle's medium whose composition was similar to that of extracellular fluid for 30 days. The precipitation of the calcium phosphate on implant surface was increased by the immersion in the NaOH solution, and more highly accelerated by heat treatment at $600^{\circ}C$. The precipitation of the calcium phosphate on titanium implant was increased with the treatment of the anodic oxidation in Hanks' solution at 5V, $80^{\circ}C$.