• Title/Summary/Keyword: hydrothemal synthesis

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Hydrothemal Synthesis of $PbTiO_3$ Powders (수열법에 의한 $PbTiO_3$ 분말 합성)

  • 박병규;이태근;이기강
    • Journal of the Korean Ceramic Society
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    • v.33 no.4
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    • pp.399-404
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    • 1996
  • Hydrothemal synthesis of PbTiO3 has been investigated. A comprehensive thermodynamic model for heteroge-nous reacting solid-aquous system has been used to predict the optimum condition for the synthesis. Synthesis were performed using lead acetate trihydrate as Pb source crystalline TiO2 as Ti source and KOH as minerali-zer. The synthesis has been examined at low temperature (16$0^{\circ}C$) Phase pure perovskite PbTiO3 has been obtained at high pH(above 0.5 mol KOH). The morphology of PbTiO3 was acicular shape. It has been found sible for a distortion in the c direction. The water is gradully released on annealing the powder to 40$0^{\circ}C$ and the normal crystallographic properties are restored.

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Conditions for the Formation of Ba-Ferrite by Hydrothermal Synthesis (수열합성에 의한 Ba-Ferrite의 형성조건)

  • 이경희;이병하;윤갑중
    • Journal of the Korean Ceramic Society
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    • v.22 no.5
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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

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Synthesis of Imogolite by a Hydrothemal Method (이모골라이트의 합성)

  • Jang, Young-Nam;Ryu, Gyoung-Won;Suh, Yong-Jae;Chae, Soo-Chun;Bae, In-Kook
    • Journal of the Mineralogical Society of Korea
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    • v.21 no.3
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    • pp.283-287
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    • 2008
  • The imogolite synthesis wore performed by using tetraethoxysilane (TEOS) and aluminium-sec-butoxide (ASB) at < $100^{\circ}C$. A mixure of TEOS and ASB in a molar ratio of 1:2 was prepared under vigorous stirring and the experiments were performed under the hydrothemal refluxing condition. When the concentration of TEOS and ASB in solution was 0.5 M, a well-crystallized imogolite was synthesized, and the reflections wore shown at d = 22.4, $9.5\;\AA$ etc., after XRD analysis. DTA analysis shows 2 exothemal peaks at 68 and $249^{\circ}C$, suggesting the dehydration and the dehyroxylation reaction, respectively. The result of TG indicates 41% weight loss. And the weak and unsymmetrical peaks by the Si-O-Al stretching vibrations at 953 and $993cm^{-1}$ and by O-Si-O bending vibration at $562cm^{-1}$ were observed after IR analysis. The synthetic imogolite was fibrous and shows a spiders web like network structure.

Synthesis of Zeolite from Waste LCD Panel Glass (폐 LCD 패널유리를 이용한 제올라이트의 합성)

  • Lee, Chul-Tae
    • Applied Chemistry for Engineering
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    • v.28 no.5
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    • pp.521-528
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    • 2017
  • To find a recycling method for waste liquid crystal display (LCD) panel glasses, we investigated the synthesis process of zeolite with an ion exchange ability by hydrothermal reaction using waste LCD panel glass as a raw material. It was shown that the waste LCD panel glass can be used as a raw material for the production of zeolites having the ion exchange ability. Following conditions for the synthesis of the zeolite with an ion exchange ability were required : the molar ratio of Si to Al components of the waste LCD glass needs to be 2.0 to 2.8, and the temperature of $100^{\circ}C$ and reaction time of 12 hours are needed for the hydrothermal reaction. Based on the required conditions previously mentioned, the A type zeolite was synthesized when the molar ratio of the Si to Al component was 2.0, and the P type zeolite was produced when the molar ratio was 2.8. The type A zeolite synthesized by using the waste LCD panel glass showed a good ion exchange ability and heavy metal adsorption ability. Also, an excellent ion exchange capacity was observed as the crystal phase grows stably in a cubic phase.

Metal Reduction and Mineral formation by fe(III)-Reducing Bacteria Isolated from Extreme Environments (철환원 박테리아에 의한 금속 환원 및 광물형성)

  • Yul Roh;Hi-Soo Moon;Yungoo Song
    • Journal of the Mineralogical Society of Korea
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    • v.15 no.3
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    • pp.231-240
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    • 2002
  • Microbial metal reduction influences the biogeochemical cycles of carbon and metals as well as plays an important role in the bioremediation of metals, radionuclides, and organic contaminants. The use of bacteria to facilitate the production of magnetite nanoparticles and the formation of carbonate minerals may provide new biotechnological processes for material synthesis and carbon sequestration. Metal-reducing bacteria were isolated from a variety of extreme environments, such as deep terrestrial subsurface, deep marine sediments, water near Hydrothemal vents, and alkaline ponds. Metal-reducing bacteria isolated from diverse extreme environments were able to reduce Fe(III), Mn(IV), Cr(VI), Co(III), and U(VI) using short chain fatty acids and/or hydrogen as the electron donors. These bacteria exhibited diverse mineral precipitation capabilities including the formation of magnetite ($Fe_3$$O_4$), siderite ($FeCO_3$), calcite ($CaCO_3$), rhodochrosite ($MnCO_3$), vivianite [$Fe_3$($PO_4$)$_2$ .$8H_2$O], and uraninite ($UO_2$). Geochemical and environmental factors such as atmospheres, chemical milieu, and species of bacteria affected the extent of Fe(III)-reduction as well as the mineralogy and morphology of the crystalline iron mineral phases. Thermophilic bacteria use amorphous Fe(III)-oxyhydroxide plus metals (Co, Cr, Ni) as an electron acceptor and organic carbon as an electron donor to synthesize metal-substituted magnetite. Metal reducing bacteria were capable of $CO_2$conversion Into sparingly soluble carbonate minerals, such as siderite and calcite using amorphous Fe(III)-oxyhydroxide or metal-rich fly ash. These results indicate that microbial Fe(III)-reduction may not only play important roles in iron and carbon biogeochemistry in natural environments, but also be potentially useful f3r the synthesis of submicron-sized ferromagnetic materials.

Synthesis of Hectorite by Hydrothemal Method (저온 수열법에 의한 헥토라이트 합성)

  • Jang, Young-Nam;Chae, Soo-Chun;Ryu, Gyoung-Won;Kim, You-Dong;Jang, Hee-Dong;Bae, In-Kook
    • Journal of the Mineralogical Society of Korea
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    • v.20 no.1 s.51
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    • pp.1-6
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    • 2007
  • Hectorite was synthesized by a two-step hydrothermal process from $Mg(OH)_{2}$, water glass (${\sim}30\;wt%\;SiO_{2}$) and Li-compound at $90{\pm}5^{\circ}C$. The product shows excellent dispersion and swelling properties. The mixture of the starting materials was heated in a glass vessel for the first reaction with continuous stirring and the pH of the solution was adjusted to $6{\sim}8$, resulting in the formation of a precursor of hectorite. The excess salt components were washed out from the resulting slurry and then was matured in the glass vessel for the 2nd reaction. Li compound was added during the reaction. After a 10 h retention, the gel of hectorite was formed. The XRD pattern of the synthesized one was coincided with that of natural hectorite and SEM study revealed uniform grains 50 m in diameter. The d001 basal spacing of the product moved from 12 to $17.4\;{\AA}$ after glycolation treatment. The measured value of CEC and the swelling capacity was 90 cmol/kg and $60{\sim}70\;mL/2\;g$, respectively.

Effect of Calcination Temperatures on the Structure and Electrochemical Characterization of Li(Ni0.5Mn0.3Co0.2)O2 as Cathode Material by Supercritical Hydrothermal Synthesis Method (초임계 수열법으로 합성한 Li(Ni0.5Mn0.3Co0.2)O2 양극 활물질의 소성 온도영향에 따른 구조 및 전기화학적 특성)

  • Choo, Soyeon;Beom, YunGyeong;Kim, Sungsu;Han, Kyooseung
    • Journal of the Korean Electrochemical Society
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    • v.16 no.3
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    • pp.151-156
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    • 2013
  • As the cathode material for li-ion battery, $LiNi_{0.5}Mn_{0.3}Co_{0.2}O_2$ were synthesized by supercritical hydrothermal method and calcined $850^{\circ}C$ and $900^{\circ}C$ for 10hrs in air. The effect of temperature in the heat treatment on the powder and its performance were studied of xray diffraction pattern, SEM-image, physical properties and electrochemical behaviors. As a result, calcined at $900^{\circ}C$ material particle size more increase than calcined at $850^{\circ}C$ material, especially shows excellent electrochemical performance with initial reversible specific capacity of 163.84 mAh/g (0.1C/2.0-4.3V), 186.87 mAh/g (0.1C/2.0-4.5V) and good capacity retention of 91.49% (0.2C/2.0-4.3V) and 90.36% (0.2C/2.0-4.5V) after 50th charge/discharge cycle.