• Journal of the Korean Ceramic Society
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• v.41 no.9
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• pp.715-721
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• 2004

Hydroxyapatite (HAp)/Gelatin (GEL) homogeneous composites of four different composition ratio were prepared by the co-precipitation process with synthetic HAp and GEL as a binder, HAP/GEL composites were molding by cold isostatic pressing and were sintering by various condition in air. Crystallinity and structure of sintered HAp/GEL composites were investigated by XRD and FTIR. Also, the compressive strength and the fracture surface of sintered specimens were measured by UTM and SEM. HAp/GEL composites showed a phase transformation to partially ${\alpha}$, ${\beta}$-tricalcium phosphate at the sintered condition of 1200$^{\circ}C$ for 3 h. The porosity of sintered body was in the range of 1.2-30.2％. The compressive strength of the sintered specimens was in the range of 16.2-60.1㎫, and its strength of sintered HAp/GEL comosites was higher than expected when the porosity was considered.

• Applied Chemistry for Engineering
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• v.7 no.5
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• pp.849-860
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• 1996

Natural zeolites which were known to occur in sedimentary clinoptilolite, were treated by thermal and chemical methods, and their adsorption characteristics of Cu(II) were studied. Analyses by FT-IR, S. E. M, TGA/DSC, and XRD showed that the adsorption capacity of Cu(II) on the zeolite decreased gradually at the temperatures of above $400^{\circ}C$. The zeolites, which treated with NaOH and NaCl, show higher absorbility in acid solution. The adsorption rate of Cu(II) in the presence of surfactants(LAS, POE AE) on the thermally or chemically treated zeolites varied depending on pH, anion or nonion surfactants.

• Resources Recycling
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• v.19 no.5
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• pp.44-49
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• 2010

SiC powders have been recovered from silicon-containing waste slurry by carbothermal reduction method with carbon black. Large amount of silicon-containing waste slurry is generated from Solar Cell industry. In an environmental and economic point of view, retrieve of the valuable natural resource from the silicon waste is important. In this study, SiC powder recovered by the reaction ball-milled silicon powder from waste and carbon black at $1350^{\circ}C$ for 3h under vacuum condition. Physical properties of samples have been characterized using SEM, XRD, Particle size analyzer and FT-IR spectroscopy.

• Journal of the Korean Crystal Growth and Crystal Technology
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• v.15 no.2
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• pp.79-85
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• 2005

Commercial hydroxyapatite (HA) powders were calcined at the temperature range of $1000{\sim}1350^{\circ}C$ in air, for 2h, and the calcined powders were immersed in simulated body fluid (SBF) of pH 7.4 at $37^{\circ}C$ for 3 or 7 days. Thermal decomposition and their related dissolution behaviors of hydroxyapatite were investigated by XRD, FT-IR, and TEM. At the temperature of $1200^{\circ}C$, HA gradually releases its $OH^-$ ions and transforms to OHAP((oxyhydroxyapatite, ($Ca_{10}(PO_4)_6O_x(OH)_{2-2x}$)). HA thermally decomposes to ${\alpha}-TCP$ (${\alpha}-tricalcium$ phosphate) and TTCP (tetracalcium phosphate) phase at $1350^{\circ}C$. It was found that the surface dissolution of the hydroxyapatite powders was accelerated by non-stoichiometric composition and decomposed to ${\alpha}-TCP$ and TTCP.

• Membrane Journal
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• v.32 no.1
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• pp.74-82
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• 2022

The objective of this work was to investigate the gas permeation properties of CO₂ and CH₄ for PEBAX^®/TS-530 hybrid membranes and compare with pure PEBAX^®-1657 membrane. With FTIR and XRD it was possible to confirm that TS-530 was dispersed well in PEBAX^® matrix. Compared with pure PEBAX^® membrane, ideal separation factor for PEBAX^®/TS-530 (10 wt%) hybrid membrane was enhanced a little. As the amount of TS-530 was increased, the gas permeability coefficients of both CO₂ and CH₄ were increased, while the ideal separation factor was decreased. This results were explained by the reduction of crystallinity of polyamide block and interchain distance caused by introduction of inorganic nanoparticles. And fumed silica might tend to agglomerate, resulting in forming nonselective nanogaps in the hybrid materials, thus the diffusivity would be enhanced at the expense of diffusivity selectivity.

• Journal of the Korean Crystal Growth and Crystal Technology
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• v.19 no.4
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• pp.165-171
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• 2009

In this study, ruby single crystals were successfully grown by flux method using an alumina crucible. The alumina crucible can be a substitute for the platinum crucible of high price. The ruby single crystals were grown in the temperature range of $915{\sim}1350^{\circ}C$ for 240 h, using $PbO-B_2O_3$ mixture. The grown ruby crystals with 9.02 ${\times}$ 6.36 mm in size exhibited red color and were transparent. The optical and structural properties were examined by UV-VIS spectrometry, FTIR and XRD. The optical properties of theses crystals were similar to those of the natural ruby and synthetic ruby grown by other methods.

• Proceedings of the Materials Research Society of Korea Conference
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• 2003.03a
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• pp.240-240
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• 2003

SiC 섬유의 고온강도를 향상시키기 위한 소결조제로 boron, aluminum 등을 사용할 수 있다. 본 연구에서는 폴리카보실란에 aluminum precursor를 첨가한 후 중합반응을 거쳐 Al-contained polycarbosilane을 합성하였다. 합성된 Al-contained polycarbosilane을 용융방사하여 섬유화 하고 열분해 공정을 통해 Si-Al-C-O 나노복합 섬유를 제조하였다. 먼저 aluminum butoxide와 polycarbosilane(commercial)을 200m1 xylene에 용해시켜 14$0^{\circ}C$에서 1시간 동안 reflux하였다. evaporator를 이용하여 xylene를 제거한 후 autoclave에서 25$0^{\circ}C$/30$0^{\circ}C$ 중합과정을 통해 가교결합 시켰다 이와 같이 합성된 시료는 ICP분석을 통해 aluminum 함량을 확인하였고 FT-IR(Fig.1) 및 GPC분석(Fig.2)으로부터 화학구조 및 분자량변화를 확인하였다. aluminum 첨가량이 증가함에 따라 Si-H/Si-$CH_3$의 결합크기의 비가 감소하였으며 이로부터 aluminum butoxide와 polycarbosilane의 가교결합이 이루어진 것으로 보이며 중합 후 분자량의 증가 또한 가교결합에 의한 결과로 사료된다 열무게감량(TGA) 측정 결과는 40$0^{\circ}C$부터 유기리간드의 분해가 일어나며 80$0^{\circ}C$이상에서 세라믹화 과정이 완료되었음을 알 수 있었다 또한 aluminum 첨가량이 증가함에 따라 세라믹 수율도 증가하였음을 확인하였다. 합성된 aluminum-contained polycarbosilane은 20$0^{\circ}C$에서 1시간 동안 불융화과정을 거쳐 환원 및 진공 분위기에서 고온 열처리하였으며 이로부터 얻어진 시료에 대해 XRD분석을 수행하였다. SEM과 TEM을 이용하여 미세구조를 관찰하였다.

• Proceedings of the Korean Vacuum Society Conference
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• 2014.02a
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• pp.471.1-471.1
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• 2014

염료감응형 태양전지(DSSC)는 다양한 태양전지 중, 가장 환경친화적이고, 생산단가도 낮을 뿐만 아니라 다양한 색상과 투광성을 확보할 수 있어 많은 연구가 진행되어왔다. 하지만 액체전해질을 사용하는 기존 염료감응형 태양전지는 높은 휘발성과 열 팽창 수축에 따른 전해질 누액의 문제점으로 인하여 최근에는 고체전해질을 이용한 염료감응형 태양전지의 개발이 활발히 이루어지고 있다. 또한 기존 염료보다 높은 흡광계수와 넓은 흡수스펙트럼을 지닌 페로브스카이트가 개발되어 현재 많은 관심이 주목되고 있다. 본 연구에서는 $TiO_2$ 제조상의 중간생성물인 Metatitanic acid (MTA)를 이용하여 광전극을 형성하고 열처리 온도에 따른 나노입자의 소성거동평가을 평가하였고 시차열중량 분석, 결정상 확인을 하고 염료감응 태양전지에 적용하였다. MTA 나노입자를 Field Emission Transmission Electron Microscopy (FE-TEM), Barrett-Joyner-Halenda (BJH pore size distribution)과 Brunauer-Emmet-Teller (BET) 분석을 통해 소성거동을 평가하고, Thermogravimetry and differential thermal analysis (TG-DTA)를 통해 열중량 측정을 하였으며, X-ray Diffraction (XRD) 분석을 통해 결정상을 확인하였다. 또한 Fourier-transform infrared (FT-IR) spectroscopy를 통해 MTA 나노입자의 표면분석을 하였다. 형성된 MTA 광전극을 페로브스카이트 염료에 적용하여 5%의 효율을 달성하였다.

• Korean Journal of Materials Research
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• v.27 no.3
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• pp.161-165
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• 2017

In this paper, synthesis of terephthalate intercalated Zn-Al: Layered double hydroxides (LDHs) was studied. We designed freestanding Zn-Al: carbonate LDH nanosheets for a facile exchange technique. The as-prepared Zn-Al carbonate LDHs were converted to terephthalate intercalated Zn-Al:LDHs by ion exchange method. Initially, Al-doped ZnO (AZO) thin films were deposited on p-Si (001) by facing target sputtering. For synthesis of free standing carbonate Zn-Al:LDH, we dipped the AZO thin film in naturally carbonated water for 3 hours. Further, Zn-Al: carbonate LDH nanosheets were immersed in terepthalic acid (TA) solution. The ion exchange phenomena in the terephthalate assisted Zn-Al:LDH were confirmed using FT-IR analysis. The crystal structure of terephthalate intercalated Zn-Al:LDH was investigated by XRD pattern analysis with different mole concentrations of TA solution and reaction times. The optimal conditions for intercalation of terephthalate from carbonated Zn-Al LDH were established using 0.3 M aqueous solution of TA for 24 hours.

• Journal of the Mineralogical Society of Korea
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• v.22 no.3
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• pp.241-248
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• 2009

Kaolinite was synthesized from amorphous $SiO_2$ and $Al(OH)_3{\cdot}xH_{2}O$ as starting materials by hydrothermal reaction conducted at $250^{\circ}C$ and $30\;kg/cm^2$. The acidity of the solution was adjusted at pH 2. The synthesized kaolinite was characterized by XRD, IR, NMR, FE-SEM, TEM and EDS to clarify the formational process according to the reaction time from 2 to 36 hours. X-ray diffraction patterns showed after 2 h of reaction time, the starting material amorphous $Al(OH)_3{\cdot}xH_{2}O$ transformed to boehmite (AlOOH) and after the reaction time 5 h, the peaks of boehmite were observed to be absent thereby indicating the crystal structure is partially destructed. Kaolinite formation was identified in the product obtained after 10 h of reaction and the peak intensity of kaolinite increased further with reaction time. The results of TGA and DTA revealed that the principal feature of kaolinite trace are well resolved. TGA results showed 13 wt% amount of weight loss and DTA analysis showed that exothermic peak of boehmite observed at $258^{\circ}C$ was decreased gradually and after 10 h of reaction time, it was disappeared. After 5 h of the reaction time, the exothermicpeak of transformation to spinel phase was observed and the peak intensiy increased with reaction time. The results of FT-IR suggested a highly ordered kaolinite was obtained after 36 hours of reaction. It was identified by the characteristic hydroxide group bands positioned at 3,696, 3670, 3653 and $3620\;cm^{-1}$. The development of the hydroxyl stretching between 3696 and $3620\;cm^{-1}$, depends on the degree of order and crystalline perfection. TEM results showed that after 15 h reaction time, curved platy kaolinite was observed as growing of (001) plane and after 36 h, the morphology of synthetic kaolinite exhibited platy crystal with partial polygonal outlines.