• Transactions on Electrical and Electronic Materials
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• v.9 no.3
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• pp.91-95
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• 2008

In this study, in order to develop the composition ceramics for low loss multilayer piezoelectric actuator application, $Pb(Zn_{1/2}W_{1/2})O_3-Pb(Mn_{1/3}Nb_{2/3})O_3-Pb(Zr,Ti)O_3$ (abbreviated as PZW-PMN-PZT)ceramics according to the amount of $MnO_2$ addition were fabricated using two-stage calcinations method. And also, their dielectric and piezoelectric properties were investigated. At the 0.2 wt% $MnO_2$ added PZW-PMN-PZT ceramics sintered at $930^{\circ}C$, density, electromechanical coupling factor $k_p$, dielectric constant ${\varepsilon}_r$, piezoelectric $d_{33}$ constant and mechanical quality factor $Q_m$ showed the optimum value of $7.84g/cm^3$, 0.543, 1,392, 318.7 pC/N, 1,536, respectively for low loss multilayer ceramics actuator application.

• Journal of Korean Society on Water Environment
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• v.25 no.3
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• pp.404-410
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• 2009

In this study, research for physical and chemical characteristics were conducted through analysis of sediments, grading and heavy metals (e.g., Mn, Cu, Cd, Zn and Pb ) in sewers which are classified by drainage types. After that, cement solidification and yellow soil calcinations made heavy metals stabilized and then, ways of recycling it were examined. The grain size distribution of all sediments was relative graded. When evaluating heavy metal pollution through index of geoaccumulation (Igeo), Cu showed moderately pollution or strong pollution in forest and street site and Zn was assessed by moderately pollution in military, residential, and street site. Analysis of Pearson Correlation coefficient of heavy metal indicated that all items in street site have tight relationship respectively. Especially, Cd-Zn, Cu-Pb, Cu-Mn, and Pb-Mn have relationship at 99% confidence intervals in statistical analysis. Recycling it with cement solidification was satisfied with compressive strength standard under 55% deposit contents and Zn, Pb, Mn were stabilized effectively. If time and temperature plasticity and compressive strength would be standard, it is revealed that yellow soil calcinations is valuable aggregate when it has 50-60 Wt% contents. When considering economic feasibility and stabilization of heavy metals, cement solidification would be more appropriate than yellow soil calcinations as solution to recycling.

• Korean Journal of Materials Research
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• v.10 no.3
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• pp.191-198
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• 2000

A serpentine mineral was treated in hydrochloric acid solution to obtain amorphous silica residue with high surface area. The highly porous silica with aluminum hydroxide and sodium hydroxide was hydrothermally reacted in an autoclave. A numerous experiments were performed in terms of reaction time, temperature, alkalinity, and calcinations temperature. As a result, a ZSM-5 zeolite of the highest crystallinity was produced under such conditions as $^170{\circ}C$ of the reaction temperature, 24 hours of the reaction time, and $11.7Na_2O{\cdot}Al_2O_3{\cdot}90SiO_2{\cdot}3510H_2O{\cdot}10.8(TPA)_2O$ the composition along with 3 hours of the calcinations at $600^{\circ}C$.

• Proceedings of the KAIS Fall Conference
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• 2001.05a
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• pp.287-289
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• 2001

The morphology of silica supported MoO$_3$ catalysts, which was prepared by impregnation of ammonium heptamolybdate with various weight loadings up to 35 wt%, was studied using x-ray diffraction. In addition to the orthorhombic phase, the behavior of the rarely studied hexagonal phase was characterized. For high loading catalysts, excess ammonium ions present in the monoclinic and triclinic precursors are capable of occupying interstitial sites of microcrystalline MoO$_3$ during moderate temperature calcinations and in doing so enhance the MoO$_3$-SiO$_2$ interaction. This results in a "well dispersed" morphology at high loadings. Sintering at high temperature is due to loss of ammonium from the oxide framework. Ammonia reimpregnation, which leads back to the well dispersed hexagonal phase, may offer a simple regeneration process for spent Mo containing catalysts.

• Journal of the Korean Institute of Electrical and Electronic Material Engineers
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• v.26 no.9
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• pp.651-655
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• 2013

$(Ba_{0.85}Ca_{0.15})(Ti_{0.9}Zr_{0.1})O_3$ + 0.04 wt% $CeO_2$ lead-free ceramics were synthesized by conventional sintering process and the effect of calcination temperature on microstructure, dielectric and piezoelectric properties were investigated. Improved piezoelectric properties have been observed at $1,125^{\circ}C$ calcination temperature which show the optimal electrical properties, $k_p$~0.457, $d_{33}$~367 pC/N, $Q_m$~158 and $T_c$~$85^{\circ}C$. These results show that the piezoelectric properties can be improved by appropriate calcination temperature.

• Bulletin of the Korean Chemical Society
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• v.27 no.3
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• pp.368-372
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• 2006

The cobalt titanate, $CoTiO_3$ nanoparticles have been prepared by calcinations of precursor obtained from a mixture of $TiO_2$ and $Co(OH)_2$ in aqueous cetyltrimethylammonium bromide (CTAB) solution. The nanoparticles were investigated with X-ray powder diffraction (XRD), transmission electron microscopy (TEM), X-ray photoelectron spectroscopy (XPS) and thermogravimetric/differential thermal analysis (TGA/DTA) to determine the crystallite size and the phase composition. The spectroscopic characterizations of these nanoparticles were also done with UV-Vis spectroscopy and FT-Raman spectroscopy. XRD patterns show that $CoTiO_3$ phase was formed at calcinations temperature above 600 ${^{\circ}C}$. UV-Vis absorption spectra indicate that the $CoTiO_3$ nanoparticles have significant red shift to the visible region (400-700 nm) with $\lambda_{max}$ = 500 nm compared to pure $TiO_2$ powder ($\lambda_{max}$ = 320 nm). The new absorption peaks (absorption at 696, 604, 520, 478,456, 383, 336, 267, 238, 208 $c m ^{-1}$), which were not appeared in FT-Raman spectra of P-25, also confirm the formation of Ti-O-Co bonds at above 600 ${^{\circ}C}$ and just not the mixtures of titanium dioxide with cobalt oxides.

• Journal of Environmental Health Sciences
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• v.31 no.6
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• pp.483-488
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• 2005

The waste seashells were used for the removal of hydrogen sulfide from a hot gas stream. The sulphidation of waste seashells with $H_{2}$S was studied in a thermogravimetric analyzer at temperature between 600 and $800^{circ}C$. The desulfurization performance of the waste seashell sorbents was experimentally tested in a fixed bed reactor system. Sulfidation experiments performed under reaction conditions similar to those at the exit of a coal gasifier showed that preparation procedure and technique, the type and the amount of seashell, and the size of the seashell affect the $H_{2}$S removal capacity of the sorbents. The pore structure of fresh and sulfided seashell sorbents was analyzed using mercury porosimetry, nitrogen adsorption, and scanning electron microscopy (SEM). Measurements of the reaction of $H_{2}$S with waste seashells show that particles smaller than 0.631 mm can achieve high conversion to CaS. According to TGA and fixed bed reactor results, temperature had influenced on $H_{2}$S removal efficiency. As desulfurization temperature increased, desulfurization efficiency increased. Also, maximum desulfurization efficiency was observed at $800^{circ}C$. Desulfurization was related to calcinations temperature.

• Korean Journal of Crystallography
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• v.15 no.1
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• pp.44-50
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• 2004

Spinel structured lithium managanese oxide $(LiMn_2O_4)$ powder with well defined facetted morphology was prepared by precipitation-evaporation method. {111}, {110}, and {100} planes are mainly observed in the $LiMn_2O_4$ powder. And powder shape of tetradecahedron and octahedron was observed depending on the calcinations temperature. The observed powder morphology observed seemed to be related to the nonstoichiometry of the oxygen in the $LiMn_2O_4$ spinel structure. Oxygen nonstoichiometry might be responsible for the Jahn-teller effect and structure transition which in turn affects the surface energy of the {111}, {110}, and {100} planes. Powder shape transition from tetradecahedron to octahedron seemed to be related to the surface energy of the {111}, {110}, and {100} planes with oxygen nonstoichiometry.

• Journal of the Korean Chemical Society
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• v.55 no.6
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• pp.1024-1029
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• 2011

PVA/silica hybrid xerogels were synthesized by sonohydrolysis of a mixture of 2-way catalyzed TEOS and water solution of PVA. PVA was successfully removed from the xerogels through calcination and its removal was confirmed through TGA analysis of the calcined gel. Microstructure of the gels was studied through SEM, XRD and FTIR. Nitrogen sorption studies were conducted to find out surface area of different samples. It was found out that the samples having PVA removed through calcinations have higher surface area (411.64 $m^2$/g) than the samples (353.544 $m^2$/g) synthesized without any PVA. Adsorption properties of these xerogels synthesized by using different ratios of components were studied by taking Rhodamine G6 as a model adsorbate. The experiments were conducted at room temperature ($25^{\circ}C$). UV visible spectroscopy was used to measure the concentration of the dye before and after adsorption. The adsorption data of Rhodamine G6 on PVA modified silica is described by the Freundlich's adsorption model.

• Proceedings of the Korean Powder Metallurgy Institute Conference
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• 2006.09a
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• pp.152-153
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• 2006

We demonstrate the methodology of engineering the multi-component ceramic nanopowder with precise morphology by nanoblast calcinations decomposition of preliminary engineered nanoreactors. Multiple explosions of just melted $C_3H_6N_6O_6$ embedded into preliminary engineered nanoreactors break apart the agglomerates due to the highly energetic impacts of the blast waves. Also, the solid-solubility of one component into the other is enhanced by the extremely high local temperature generated during each nano-explosion in surrounding area. This methodology was applied for production of agglomeratefree nano-aggregates of $Gd_{20}Ce_{80}O_{1.95}$ with an average size of 42 nm and $LaSrGaMgO_{3-x}$ nanopowder with an average aggregate size of 83 nm.