• 한국세라믹학회지
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• 제51권2호
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• pp.115-120
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• 2014

Quicklime(CaO) is generally obtained through the calcination of limestone, the main component of which is calcium carbonate($CaCO_3$). Quicklime generates high-temperature heat when reacting with water, forming slaked lime($Ca(OH)_2$). The industrial sectors for limestone are determined by the hydraulic activity of slaked lime, which is obtained by measuring temperature changes during the hydration reaction. Accordingly, this study examined the different crystallographic characteristics of limestone as affected by the geological origins of the regions where the limestones were produced, and how these characteristics affected hydraulic activity. Six limestone samples were collected from the Jecheon and Cheongsong areas and the hydraulic activities were measured in accordance with KS E 3077. The results indicate that limestone produced in the Cheongsong area, recrystallized through metamorphism caused by hydrothermal alteration, hada larger grain size of calcite than that of the Jecheon area, and displays a tendency of changing to marble. Limestone from the Cheonsong area showed more radical reaction in the early stage of hydration compared to that ofthe Jecheon area. In addition, it was revealed that limestone having more impurities like $SiO_2$ have lower hydraulic activity.

• Bulletin of the Korean Chemical Society
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• 제34권8호
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• pp.2271-2275
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• 2013

We report on the photoelectrochemical properties of partially reduced mesoporous titania thin films. The fabrication is achieved by synthesizing mesoporous titania thin films through the self-assembly of a titania precursor and a block copolymer, followed by aging and calcination, and heat-treatment under a $H_2$ (1 torr) environment. Depending on the temperature used for the reaction with $H_2$, the degree of the reduction (generation of oxygen vacancies) of the titania is controlled. The oxygen vacancies induce visible light absorption, and decrease of resistance while the mesoporosity is practically unaltered. The photoelectrochemical activity data on these films, by measuring their photocurrent-potential behavior in 1 M NaOH electrolyte under AM 1.5G 100 mW $cm^{-2}$ illumination, show that the three effects of the oxygen vacancies contribute to the enhancement of the photoelectrochemical properties of the mesoporous titania thin films. The results show that these oxygen deficient $TiO_2$ mesoporous thin films hold great promise for a solar hydrogen generation. Suggestions for the materials design for improved photoelectrochemical properties are made.

• 자원리싸이클링
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• 제7권4호
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• pp.50-54
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• 1998

원하는 전자기적 특성인 높은 초투자율과 우수한 주파수 의존특성을 얻기 위해 Mn-Zn 페라이트계에서 핵입자의 첨가효과를 실험하였다. 소결온도에서 가소된 핵입자를 첨가함에 따라 비정상 입자성장이 말끔히 사라졌지만, 페라이트의 소결밀도와 초투자율이 감소하였다. 이와 반대로 매트릭스 입자의 가소온도보다 낮은 온도에서 가소된 핵입자의 첨가시에는 비정상 입자성장이 잔유하였으나, 적정한 핵입자 첨가로 Cutoff Frequency가 변화하지 않는 가운데 10∼20%의 초투자율값의 상승이 있었다.

• 상하수도학회지
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• 제34권1호
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• pp.1-8
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• 2020

In this study, the physicochemical characteristics and fluoride adsorption capacity of the bone char pyrolyzed at different temperatures; 200℃, 300℃, 350℃, 400℃, 500℃, 600℃, and 700℃ were investigated. Analytical studies of the synthesized bone char including; SEM-EDS, XRD, BET and FT-IR, showed the presence of hydroxyapatite(HAP), which is the main substance that adsorbs fluoride from aqueous solutions containing high fluoride concentrations. Bone char pyrolyzed from 350~700℃ specifically revealed that, the lower the temperature, the higher the fluoride adsorption capacity and vice versa. The loss of the fluoride adsorption function of HAP (OH^- band in the FTIR analysis) was interpreted as the main reason behind this inverse correlation between temperature and fluoride adsorption. Bone char produced at 350℃ hence exhibited a fluoride adsorption capacity of 10.56 mgF/g, resulting in significantly higher adsorption compared to previous studies.

• 한국재료학회지
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• 제2권1호
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• pp.3-11
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• 1992

점토 광물로부터 황산 처리법을 이용하여 수화 황산 알루미늄을 제조하였다. 하동 카올린 을 황산 처리하였을 때 수화 황산 알루미늄 형성에 미치는 카올린의 하소 온도와 하소 시간, 산처리 반응 온도와 반응 시간 및 황산의 농도의 영향을 조사하였다. 또한, 황산 처리된 용액으로부터 수화 황산 알루미늄이 석출되는 최적 조건을 구하였으며, 생성된 수화 황산 알루미늄을 상온에서 $1200^{\circ}C$ 까지 각각의 온도 구간에서 열처리한 분말에 대해서 XRD, TG-DTA, FT-IR, SEM, 입도 분석 및 불순물 분석을 하였다. 최적 조건 하에서, 카올린 중의 알루미나가 수화 황산 알루미늄으로 생성되는 전화율은 약 60%였고, XRD, TG-DTA, FT-IR 등의 분석 결과로 부터 생성된 수화 황산 알루미늄의 열분해 반응은 $Al_2(SO_4)_3{\cdot}18H_2O{\rightarrow}Al_2(SO_4)_3{\cdot}6H_2O{\rightarrow}Al_2(SO_4){\rightarrow}\;amorphous\;alumina{\rightarrow}{\gamma}-alumina{\rightarrow}{\delta}-alumina{\rightarrow}{\theta}-alumina{\rightarrow}{\alpha}-alumina$이었다. 또한 생성된 수화 황산 알루미늄을 $1200^{\circ}C$에서 하소 하여 얻은 알루미나 분말의 순도는 99.99%였다.

• 한국재료학회지
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• 제22권5호
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• pp.253-258
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• 2012

Activated magnetite ($Fe_3O_{4-{\delta}}$) was applied to reducing $CO_2$ gas emissions to avoid greenhouse effects. Wet and dry methods were developed as a $CO_2$ removal process. One of the typical dry methods is $CO_2$ decomposition using activated magnetite ($Fe_3O_{4-{\delta}}$). Generally, $Fe_3O_{4-{\delta}}$ is manufactured by reduction of $Fe_3O_4$ by $H_2$ gas. This process has an explosion risk. Therefore, a non-explosive process to make $Fe_3O_{4-{\delta}}$ was studied using $FeC_2O_4{\cdot}2H_2O$ and $N_2$. $FeSO_4{\cdot}7H_2O$ and $(NH_4)_2C_2O_4{\cdot}H_2O$ were used as starting materials. So, ${\alpha}-FeC_2O_4{\cdot}2H_2O$ was synthesized by precipitation method. During the calcination process, $FeC_2O_4{\cdot}2H_2O$ was decomposed to $Fe_3O_4$, CO, and $CO_2$. The specific surface area of the activated magnetite varied with the calcination temperature from 15.43 $m^2/g$ to 9.32 $m^2/g$. The densities of $FeC_2O_4{\cdot}2H_2O$ and $Fe_3O_4$ were 2.28 g/$cm^3$ and 5.2 g/$cm^3$, respectively. Also, the $Fe_3O_4$ was reduced to $Fe_3O_{4-{\delta}}$ by CO. From the TGA results in air of the specimen that was calcined at $450^{\circ}C$ for three hours in $N_2$ atmosphere, the ${\delta}$-value of $Fe_3O_{4-{\delta}}$ was estimated. The ${\delta}$-value of $Fe_3O_{4-{\delta}}$ was 0.3170 when the sample was heat treated at $400^{\circ}C$ for 3 hours and 0.6583 when the sample was heat treated at $450^{\circ}C$ for 3 hours. $Fe_3O_{4-{\delta}}$ was oxidized to $Fe_3O_4$ when $Fe_3O_{4-{\delta}}$ was reacted with $CO_2$ because $CO_2$ is decomposed to C and $O_2$.

• Advances in Energy Research
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• 제5권1호
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• pp.13-29
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• 2017

The roles of Na, Mn, W and silica, and the synergistic effects between each metal in the $MnNa_2WO_4/SiO_2$ catalyst have been investigated for oxidative coupling of methane (OCM). The crystallisation of amorphous silica during calcination at $900^{\circ}C$ was promoted primarily by Na, but Mn and W also facilitated this process. The interaction between Na and Mn tended to increase the extent of conversion of $Mn_3O_4$ to $Mn_2O_3$. The formation of $Na_2WO_4$ was dependent on the order in which Na and W were introduced to the catalyst. The impregnation of W before Na resulted in the formation of $Na_2WO_4$, but this did not occur when the impregnation order was reversed. $MnWO_4$ formed in all cases where Mn and W were introduced into the silica support, regardless of the impregnation order; however, the formation of $MnWO_4$ was inhibited in the presence of Na. Of the prepared samples in which a single metal oxide was introduced to silica, only $Mn/SiO_2$ showed OCM activity with significant oxygen conversion, thus demonstrating the important role that Mn plays in promoting oxygen transfer in the reaction. The impregnation order of W and Na is critical for catalyst performance. The active site, which involves a combination of Na-Si-W-O, can be formed in situ when distorted $WO_4^{2-}$ interacts with silica during the crystallisation process facilitated by Na. This can only occur if the impregnation of W occurs before Na addition, or if the two components are introduced simultaneously.

• 대한금속재료학회지
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• 제50권3호
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• pp.201-205
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• 2012

The effects of various manganese precursors for the low-temperature selective catalytic reduction (SCR) of $NO_x$ were investigated in terms of structural, morphological, and physico-chemical analyses. $MnO_x/TiO_2$ catalysts were prepared from three different precursors, manganese nitrate, manganese acetate(II), and manganese acetate(III), by the sol-gel method. The manganese acetate(III)-$MnO_x/TiO_2$ catalyst tended to suppress the phase transition from the anatase structure to the rutile or the brookite after calcination at $500^{\circ}C$ for 2 h. It also had a high specific surface area, which was caused by a smaller particle size and more uniform distribution than the others. The change of catalytic acid sites was confirmed by Raman and FT-IR spectroscopy and the manganese acetate(III)-$MnO_x/TiO_2$ had the strongest Lewis acid sites among them. The highest de-NOx efficiency and structural stability were achieved by using the manganese cetate(III) as a precursor, because of its high specific surface area, a large amount of anatase $TiO_2$, and the strong catalytic acidity.

• 자원환경지질
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• 제56권6호
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• pp.899-909
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• 2023

본 연구는 전통적으로 채색문화유산의 백색 무기안료로 사용된 호분안료를 대상으로 패각의 종류 및 소성 여부에 따른 재료과학적 특성을 분석하고, 보존환경 안정성을 평가하였다. 이를 위해 벚굴, 대합 패각 2종으로 제조된 호분과 이를 1,150 ℃에서 소성한 호분 2종을 수집하였다. 성분분석 결과, 소성 전의 호분안료는 calcite, aragonite 등의 탄산칼슘이고, 소성 후에는 portlandite가 주구성 물질로 calcite가 혼재되어 있었다. FE-SEM분석 결과, 소성 전에는 패각 종류에 따라 고유의 입형 조직을 보이지만 소성 후에는 다공성 입자의 조직 형태로 변하였다. 이에 따라 안료의 흡유량이 상당히 커지는 것을 볼 수 있다. 또한 소성 전보다 소성 후 백색도가 향상되는데, 대합 호분 안료(CS)의 색도 개선율이 더 높았다. 촉진내후성 시험 결과, 호분안료 채색시편은 시험 후 색차값이 2미만으로 육안으로 인지하기 어려운 정도였다. 특히 소성 전에 비해 소성 후 호분안료의 색차값이 작은 것으로 색 안정성이 높아진 것을 알 수 있다. 반면 소성 전보다 소성 후 시편에서 채색층 도막의 안정성이 떨어지는 것을 확인하였다. 항진균 효과는 공시균으로 Aspergillus niger, Tyromyces palustris, Trametes versicolor를 사용하였고, 호분안료가 곰팡이균에 대한 예방 보호적 효과가 있는 것으로 드러났다. 특히 소성과정을 거친 안료의 항진균 효과가 우수했는데, 이는 안료의 재료적 특성상 염기성이 강해진 것에 기인된 결과로 판단된다.

• 한국재료학회지
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• 제22권2호
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• pp.78-81
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• 2012

$Y_2O_3$ nanomaterials have been widely used in transparent ceramics and luminescent devices. Recently, many studies have focused on controlling the size and morphology of $Y_2O_3$ in order to obtain better material performance. $Y_2O_3$ powders were prepared under a modified solvothermal condition involving precipitation from metal nitrates with aqueous ammonium hydroxide. The powders were obtained at temperatures at $250^{\circ}C$ after a 6h process. The properties of the $Y_2O_3$ powders were studied as a function of the solvent ratio. The synthesis of $Y_2O_3$ crystalline particles is possible under a modified solvothermal condition in a water/ethylene glycol solution. Solvothermal processing condition parameters including the pH, reaction temperature and solvent ratio, have significant effects on the formation, phase component, morphology and particle size of yttria powders. Ethylene glycol is a versatile, widely used, inexpensive, and safe capping organic molecule for uniform nanoparticles besides as a solvent. The characterization of the synthesized Y2O3 powders were studied by XRD, SEM (FE-SEM) and TG/DSC. An X-ray diffraction analysis of the synthesized powders indicated the formation of the $Y_2O_3$ cubic structure upon calcination. The average crystalline sizes and distribution of the synthesized $Y_2O_3$ powders was less than 2 um and broad, respectively. The synthesized particles were spherical and hexagonal in shape. The morphology of the synthesized powders changed with the water and ethylene glycol ratio. The average size and shape of the synthesized particles could be controlled by adjusting the solvent ratio.