• 한국세라믹학회지
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• 제22권5호
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• pp.61-65
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• 1985

This stud deals with the conditions for the Formation of Ba-Ferrite by Hydrothemal synthesis Suspensions Containing either iron(III) hydroxide or hydroxide oxide and barium ians were subjected to autoclavings at various temperatures from 150 to 30$0^{\circ}C$. A ferromagnetic precipitate BaO.$6Fe_2O_3$ consisting of hexagonal plate-like particle was obtained by suitable combination of temperature and concentration of KOH

• 한국세라믹학회지
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• 제28권9호
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• pp.739-749
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• 1991

Calcium hydroxide fine powders were synthesized by hydration of calcium oxide, and the shapes of powders obtained were examined for each synthethic condition. When distilled water was used as a solvent, irregular and agglomerated submicron powders were obtained, and it was impossible to control of the shapes. In methanol-added solutions, hexagonal plate-like particles were obtained, but addition of ethanol had no effect. However on the occasion that substituted ethylene glycol for ethanol of 5 vol%, hexagonal plate-like powders were obtained. The shapes of powders synthesized in acetic acid and salicylic acid solutions were hexagonal platelike, and were spherical and very fine in citric acid and oxalic acid solutions, respectively. But in some solutions, calcium salts were precipitated by the reaction between calcium and acid added. And the size of powders were very fine using ultrasonic vibration instead of mechanical agitation.

• 한국세라믹학회지
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• 제24권3호
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• pp.215-222
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• 1987

${\alpha}$-Ferric Hydrous Oxide and ${\alpha}$-Ferric Oxide were obtained as following processes that Ferric Nitrate solution was adjusted to pH 6-8 with Ammonium Hydroxide, refluxed the Iron precipitate for 1 hr. at 80$^{\circ}C$, washed it with water and Methanol (95%), dried it to obtain ${\alpha}$-Ferric Hydrous Oxide at 60$^{\circ}C$, and then heated in atmosphere to prepare ${\alpha}$-Ferric Oxide for 1 hr. at 450$^{\circ}C$. Mica particles cleaned with ultrasonicator (45KHz) in water were mixed with Ferric Nitrate solution and treated it to adsorb ${\alpha}$-Ferric Oxide on the surface of mica particles by using the abovementioned processes, but the heated temperature was at 500$^{\circ}C$. The maximum wavelength of reflected light on the surface of mica-${\alpha}$-Ferric Oxide (50%) was appeared at 546nm but -Ferric Oxide free mica only was at 436 nm. The maximum wavelength was shifted to longer when the weight ratios of ${\alpha}$-Ferric Oxide to mica was changed from 1% to 50%.

• Restorative Dentistry and Endodontics
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• 제13권2호
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• pp.307-322
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• 1988

The purpose of this study is to evaluate the pulpal responses to the base materials such as zinc oxide eugenol cement, calcium hydroxide, zinc phosphate cement, polycarboxylate cement and glass ionomer cement. The 100 caries free dog teeth were devided into 2 groups by remaining dentin thickness (Group A: 0.4-0.6 mm, Group B: 0.8-1.0 mm) and each group were devided into 5 subgroups. The intervals of observation period are 3days, 1 week, 2 weeks, 4 weeks and 8 weeks respectively after experiment. The specimens were fixed with 10% formalin and decalcifed in 5% nitric acid. All specimens were stained with Hematoxylin-Eosin and examined histopathologically. The results were as follows. 1. In group A, atropy or hyperplasia in odontoblasts were seen in zinc oxide eugenol cement, calcium hydroxide and zinc phosphate cement. No changes in odontoblasts were seen in polycarboxylate cement and glass ionomer cement. 2. In group A, increase of predentin were seen in all experimental materials. 3. In group A, vascular congestion were seen in all experimental materials and inflammation were seen on 3 days in zinc oxide eugenol cement, 8 weeks in zinc phosphate cement and hemorrage were seen on 3 days in zinc phosphate cement. 4. In group B, changes of odontoblasts were not seen all experimental materials. 5. In group B, increase of predentin and vascular congestion were seen in all experimental materials but inflammation were not seen.

• 한국토양비료학회지
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• 제17권2호
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• pp.147-154
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• 1984

수산화철 및 알루미늄 광물을 함유하는 토양의 물리화학적 및 표면 전하의 특성을 보다 정확히 이해하기 위하여 $FeCl_3$와 $AlCl_3$ 용액으로부터 두 종류의 수산화철광물(A와 B) 및 수산화알루미늄 광물을 합성하였다. X-ray 회절분석에 의하여 수산화철 A광물은 무정형, B광물은 다량의 무정형과 함께 goethite광물이 존재하는 것으로 밝혀졌다. $105^{\circ}C$에서 건조한 결과 A광물은 소량의 무정형과 함께 akaganeite 광물, B광물은 순수 goethite로 변하였다. 한편 합성된 수산화알루미늄 광물은 gibbsite와 bayerite 광물이 약 7:3의 비율로 혼합된 것으로 밝혀졌다. 유리 또는 무정형의 철과 알루미늄을 선택적으로 용출하는 것으로 알려진 dithionite와 oxalate용액을 이용하여 이들 수산화물을 세척한 결과 dithionite가 철 용출력은 가장 강했으나 oxalate에 의한 알루미늄 용출만이 수산화알루미늄 광물중의 무정형 광물 함량을 감소하고 결정성 광물의 결정도를 높였다. 타 광물과 달리 수산화철 A광물에서 dithioite에 의한 철의 용출이 가장 많았으나 냉동건조를 제외한 건조($105^{\circ}C$의 열건조 및 $P_2O_5$ 건조)에 의하며 그 용출량이 급격히 감소하였다. 수산화철 A광물의 표면적이 가장 컸으며 역시 냉동 건조를 제외한 건조처리에 의하여 그 표면적이 현저히 감소하였고, 이들 광물중의 점토($2{\mu}m$이하)함량도 표면적의 변하와 같은 경향을 보였다. 또한 표면 전하의 절대량 발달도 수산화철 A광물이 가장 컸으며 이들 광물들의 등전점은 각각 수산화철 A광물이 8.0-8.5사이, B광물이 7.5-8.0사이로써 높았고 수산화알루미늄 광물이 5.5-6.0 사이로써 낮았다.

• 한국결정성장학회지
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• 제34권4호
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• pp.117-124
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• 2024

산화아연 나노입자는 수산기(-OH)가 포함된 에틸렌 글리콜을 이용하여 폴리올 방법으로 제조하였다. 폴리올 방법으로 생성된 아연 화합물은 하이드록시탄산아연(Zinc carbonate hydroxide, Zn₅(OH)₆(CO₃)₂)과 산화아연(ZnO) 결정구조가 혼재함을 확인하였다. 400℃, 600℃ 및 800℃에서 하소하여, 하소 온도 조건에 따른 산화아연 입자 크기, 형상 및 결정성 영향을 확인하였다. 증류수를 이용한 황산 아연 전구체 용액과 에틸렌 글리콜이 첨가된 혼합 용액으로 제조된 황산 아연 전구체 용액을 각각 800℃에서 하소하여 제조된 산화아연 분말을 입도 분석하였다. 전자의 경우 약 404 ± 51 nm의 입자 크기를 갖는 반면, 후자의 경우 약 109 ± 29 nm로 보다 균일한 나노 입자 형태의 산화아연 제조가 가능하였다. 에틸렌 글리콜을 통해 물 분자 영향을 제어하여 직접적인 산화아연 제조 및 나노 입자 크기 형태로 제조가 가능함을 제시하였다.

• 원예과학기술지
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• 제28권6호
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• pp.1072-1077
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• 2010

본 실험은 7가지의 칼슘제제; calcium sulfate dihydrate, calcium chloride, calcium nitrate, calcium oxide, calcium hydroxide, calcium carbonate, calcium hydride가 포함된 PDA배지에서 잿빛곰팡이 균의 방제효과를 알고자 실시되었다. 선발된 칼슘제제의 pH는 8.2-10으로 대조구인 pH 6.6보다는 높게 측정되었다. 7가지 칼슘제제가 포함된 PDA배지에서의 잿빛곰팡이병 방제 colony size(mm) 결과는 calcium carbonate, calcium oxide, calcium hydride, calcium hydroxide가 다른 칼슘제제들 보다 잿빛곰팡이병 억제에 효과가 좋았다. 선택된 4개의 칼슘제제를 식물체에 처리 한 후 잿빛곰팡이병의 포자를 살포한 실험과 희석된 4개의 칼슘제제)를 표준 양액재배에 첨부하여 한 달간 양액을 공급한 후 잿빛곰팡이병의 포자를 접종한 실험결과는 칼슘제제를 처리하지 않은 대조구보다는 칼슘제제를 처리한 실험구에서 잿빛곰팡이병의 발생률이 대체적으로 낮았다. 칼슘제제를 처리한 파프리카 식물체에서 잿빛곰팡이병 억제에 대하여서는 칼슘제제 처리에 따른 어느 정도의 염기스트레스의 영향 등으로 볼 수가 있겠다.

• Restorative Dentistry and Endodontics
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• 제37권4호
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• pp.188-193
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• 2012

Mineral trioxide aggregate (MTA) was developed in early 1990s and has been successfully used for root perforation repair, root end filling, and one-visit apexification. MTA is composed mainly of tricalcium silicate and dicalcium silicate. When MTA is hydrated, calcium silicate hydrate (CSH) and calcium hydroxide is formed. Formed calcium hydroxide interacts with the phosphate ion in body fluid and form amorphous calcium phosphate (ACP) which finally transforms into calcium deficient hydroxyapatite (CDHA). These mineral precipitate were reported to form the MTA-dentin interfacial layer which enhances the sealing ability of MTA. Clinically, the use of zinc oxide euginol (ZOE) based materials may retard the setting of MTA. Also, the use of acids or contact with excessive blood should be avoided before complete set of MTA, because these conditions could adversely affect the hydration reaction of MTA. Further studies on the chemical nature of MTA hydration reaction are needed.

• 한국표면공학회지
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• 제51권6호
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• pp.365-371
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• 2018

1D core-shell nanostructures have attracted great attention due to their enhanced physical and chemical properties. Specifically, oriented single-crystalline $TiO_2$ nanorods or nanowires on a transparent conductive substrate would be more desirable as the building core backbone. However, a facile approach to produce such structure-based hybrids is highly demanded. In this study, a three-step hydrothermal method was developed to grow NiMn-layered double hydroxide-decorated $TiO_2$/carbon core-shell nanorod arrays on transparent conductive fluorine-doped tin oxide (FTO) substrates. XRD, SEM, TEM, XPS and Raman were used to analyze the obtained samples. The in-situ fabricated hybrid nanostructured materials are expected to be applicable for photoelectrode working in water splitting.

• 한국폐기물자원순환학회지
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• 제34권5호
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• pp.468-473
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• 2017

This study was carried out to examine the characteristics of hydrogen sulfide adsorption using an iron hydroxide-based adsorbent. The prepared adsorbent was discussed with regard to its adsorption capacity and analyzed via surface analysis methods to illustrate the physical characteristics of hydrogen sulfide adsorption. As the drying temperature increased, the adsorption capacity of the adsorbent decreased from 29.15wt% to 22.73wt%. The adsorption capacity was decreased as the space velocity increased and showed an adsorption capacity of about 3.65 at $3,157.6h^{-1}$. The effect of sulfur dioxide was to decrease the adsorption capacity from 29.15wt% to 27.94wt%. The adsorbent exhibited the amorphous type in its physical appearance based on XRD and EDS analysis.