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241.
Chuer Hyun Moon S.K. Singh Dong Gi Lee Soung Soo Yi Kiwan Jang Jung Hyun Jeong Jong-Seong Bae Dong-Soo Shin 《Ceramics International》2012
Alkaline earth metal gallets have been identified as an important ceramic material. The crystal chemistry of many of these gallets is well explored; however, very rare studies regarding optical properties of rare earth (RE) ions doped in such gallets, particularly in Sr3Ga2O6 host, have been carried out. The present study reports on synthesis and characterization of novel Sr3Ga2O6:Eu3+ phosphors. The phosphors have been synthesized using a conventional solid state reaction method. Crystal structure, morphology and luminescence properties (excitation, emission and CIE coordinate) of these phosphors have been studied as a function of sintering temperature and Eu3+ concentration. X-ray diffraction study reveals that the phosphor sintered at low temperature (900 °C) contains an impurity phase which is removed at higher sintering temperatures and results into cubic crystalline phase of Sr3Ga2O6. Particle size of the phosphor increases with an increase in sintering temperature which results to a red shift in the peak position of excitation band lying in a broad range from 250 to 370 nm. Optimum emission intensity is attained for 0.12 mol% concentration of Eu3+ ions; above this concentration, a quenching in emission intensity is observed. 相似文献
242.
Jae-Hyun Jung Byung-Dong Hahn Woon-Ha Yoon Dong-Soo Park Jong-Jin Choi Jungho Ryu Jong-Woo Kim Cheolwoo Ahn Kie-Moon Song 《Journal of the European Ceramic Society》2012,32(10):2451-2457
Dense yttria, erbia and dysprosia films with thicknesses of 44.8 ± 1.7, 51.6 ± 0.9 and 36.8 ± 3.1 μm, respectively, were deposited on plasma sprayed alumina coating by aerosol deposition (AD). The rare earth oxide films remarkably enhanced the erosion resistance of the plasma sprayed alumina coating upon exposure to the halogen gas plasma. The enhanced plasma erosion resistances were related to their low surface porosity as well as the low vapor pressures of the rare earth fluorides and chlorides compared with those of corresponding aluminum halogenides. Electrical breakdown voltages of the samples with yttria, erbia and dysprosia films on the plasma sprayed alumina coating were 5.5, 6.2 and 5.3 kV, respectively, at room temperature and 4.0, 4.2 and 3.9 kV, respectively, at 573 K. The breakdown voltages at RT and 573 K were more than double that of the plasma sprayed alumina coating without the AD films. 相似文献
243.
Deuk-Ju Kim Hae-Young Hwang Sam-bong Jung Sang-Yong Nam 《Journal of Industrial and Engineering Chemistry》2012,18(1):556-562
Polymer nanocomposite membranes based on sulfonated poly(arylene ether sulfonate) (SPAES) containing a flake filler (Laponite) with varying degrees of sulfonation, were prepared and characterized for application in direct methanol fuel cells (DMFCs). Unlike most other clays, Laponite crystals are very small in size with a very low aspect ratio (diameter to thickness ratio) of 25–30. They improve the mechanical, thermal properties and decreased the fuel permeability. However, polymer composite membranes containing non-proton conducting inorganic particles tend to show low proton conductivity, as compared with pristine polymer membranes. To resolve this problem, prior to the preparation of the composite membranes, Laponite-Na+(NLa) was sulfonated with various amounts of organo silanes (3-Mercaptopropyl trimethoxysilane (SH-silane)) via an ion exchange method. Functionalized Laponite with the organic silane compound showed higher ion exchange capacity and ion conductivity, respectively. In order to minimize the loss of proton conductivity while reducing the methanol permeability, various amounts (0.5–2.0 wt%) of the organically sulfonated Laponite (SLa) were introduced into the SPAES matrices. The performances of hybrid membranes for DMFCs in terms of mechanical properties, behavior of water in membranes, proton conductivity and methanol permeability were investigated. 相似文献
244.
Jae Min Bak Gourishanker Jha Eungjin Ahn Seo-Hyun Jung Han Mo Jeong Byeong-Su Kim Hyung-il Lee 《Polymer》2012,53(16):3462-3468
A series of densely grafted poly(n-butyl acrylate) (PBA) molecular brushes with four different grafting densities were synthesized by the “grafting-from” approach using atom transfer radical polymerization (ATRP). A novel monomer, isopropylidene-2,2-Bis(methoxy)propionic hydroxyethylmethacrylate (IMPHMA), was synthesized and copolymerized with methyl methacrylate (MMA) under different monomer feed ratios to yield a series of linear poly(methyl methacrylate-stat-IMAPA), [PMMA-s-(PIMPHMA)]. The resulting copolymers were deprotected and transformed to macroinitiators, [PMMA-s-(PHEMA-IMPHMA-Br)]. n-Butyl acrylate (BA) was grafted from these macroinitiators to yield a series of molecular brushes, [PMMA-s-{(PIMPHMA)-g-PBA}], with various side chain lengths. Molecular brushes were characterized by gel permeation chromatography (GPC) and 1H NMR. PBA side chains were cleaved by acid hydrolysis, and the resulting linear PBA polymers were characterized by GPC to study initiation efficiency during the synthesis of molecular brushes. The initiation efficiency increased with polymerization time and decreased with macroinitiators that had more initiation sites. Atomic force microscopy (AFM) measurements demonstrated the characteristic molecular structure by resolving individual brush molecules. 相似文献
245.
Woojin Lee Hoechang Kim Dae-Ryong Jung Jongmin Kim Changwoo Nahm Junhee Lee Suji Kang Byungho Lee Byungwoo Park 《Nanoscale research letters》2012,7(1):672
The effects of surface passivation on the photoluminescence (PL) properties of CdS nanoparticles oxidized by straightforward H2O2 injection were examined. Compared to pristine cadmium sulfide nanocrystals (quantum efficiency ≅ 0.1%), the surface-passivated CdS nanoparticles showed significantly enhanced luminescence properties (quantum efficiency ≅ 20%). The surface passivation by H2O2 injection was characterized using X-ray photoelectron spectroscopy, X-ray diffraction, and time-resolved PL. The photoluminescence enhancement is due to the two-order increase in the radiative recombination rate by the sulfate passivation layer. 相似文献
246.
We report a simple, cost-effective, and environmentally benign process for reducing graphite oxide by treating solely with sulfuric acid. The suggested process consists of a two-step reduction of graphite oxide, first in aqueous sulfuric acid at room temperature and then in concentrated sulfuric acid with refluxing. X-ray diffractometry, X-ray photoelectron spectroscopy, Raman spectroscopy and thermogravimetric analysis demonstrated that the graphite oxide was reduced effectively and was comparable in composition to reduced graphite oxide prepared using previously described methods that rely on toxic and hazardous reducing agents, such as hydrazine, sodium borohydride, or hydrohalic acids. 相似文献
247.
Jeongah Lee Yeonsu Jung Junyoung Song Jun Suk Kim Geon-Woong Lee Hee Jin Jeong Youngjin Jeong 《Carbon》2012,50(10):3889-3896
We have created a field emitter composed of a carbon nanotube (CNT) yarn, which was prepared by direct spinning through chemical vapor deposition and then formed into a carpet structure by tying the yarn to a conductive substrate before cutting it. The structure of the carpet is arranged to induce the tips of the CNT yarn to protrude toward the anode for maximum electron emission. The turn-on field, threshold field, and field enhancement factor of the device are 0.33, 0.48 V/μm, and 19,141, respectively. Extremely low operating electric fields and a high field enhancement factor result from the high density of CNT emitters with high crystallinity, the electrically good contact between the emitters and the substrate, and the effects of the multistage structure. The emission is stable even at a high current density of 2.13 mA/cm2, attributed to the strong adhesion between the emitters and the substrate. The emission performance is found to be customizable by adjusting the structure, for example, the CNT pile density. These results are relevant for practical applications, such as large-area flat-panel displays, large-area low-voltage lamps, and X-ray sources. 相似文献
248.
In this study, calcium silicate hydrate (C-S-H) is synthesized and characterized. C-S-H slurry was made with calcium oxide (CaO) to micro-silica (SiO2) mixture ratio of 1.5 and enough deionized water. The slurry was continuously mixed for 7 days, then the excess water was removed. Two methods of drying were implemented: one method used the standard d-dry technique and the other was equilibrated to 11% relative humidity (RH). The dried powders were characterized using thermo gravimetric analysis (TGA), X-ray diffraction analysis (XRDA), and 29Si magic angle spinning (MAS) nuclear magnetic resonance (NMR) spectroscopy. The stoichiometric formulas of synthetic C-S-H powders dried to d-dry and 11% RH in this study were approximated as C1.2SH0.7 and C1.2SH2.4 respectively. The powders were then compacted to create specimens with porosities similar to C-S-H in hydrated cement. The specimens underwent nanoindentation to mechanically characterize C-S-H. The experiments provide insight on the nanoscale mechanical characteristics of C-S-H. 相似文献
249.
Eun-Hee Kim Geun-Ho Jo Je-Hyun Lee Yeon-Gil Jung Jaehwan Ha Ungyu Paik 《Ceramics International》2012,38(4):2749-2755
A new coating process in the powder preparation for a shell mold has been developed to increase the fracture strength of the shell mold. It is due to the homogeneous formation of a glass phase on the starting particles and the increase in the glassification efficiency by the reduction in the loss of inorganic precursors. The inorganic binder system used for the new coating process is composed of tetraethyl orthosilicate (TEOS) and sodium methoxide (NaOMe) as the silica (SiO2) and sodium oxide (Na2O) precursors, respectively. Three different coating processes are employed for the powder preparation with a high glassification efficiency. In process I, the starting particles are coated with NaOMe, and then TEOS are coated on the particles treated with NaOMe. Process II is the reverse sequence of process I. Process III involves coating of the particles with a mixture of TEOS and NaOMe. The particles coated with an individual or mixture precursor were fixed with an organic binder and then heated at 1000 °C for 1 h. Molds prepared through the new coating processes, especially process III, show a higher fracture strength value compared with that of the conventional convert mold process, which may be caused by the increase in the glassification efficiency of the precursors. Powder prepared by process III shows a more uniform coating of the glass phase than those by other processes, resulting from an enhancement in the phase mixing between SiO2 and NaOH molecules. 相似文献
250.
Sunhwan Hwang Joongwon Lee Ung Gi Hong Ji Chul Jung Dong Jun Koh Hyojun Lim Changdae Byun In Kyu Song 《Journal of Industrial and Engineering Chemistry》2012,18(1):243-248
Mesoporous nickel(30 wt%)-M(10 wt%)-alumina xerogel (30Ni10MAX) catalysts with different second metal (M = Fe, Ni, Co, Ce, and La) were prepared by a single-step sol–gel method for use in the methane production from carbon monoxide and hydrogen. In the methanation reaction, yield for CH4 decreased in the order of 30Ni10FeAX > 30Ni10NiAX > 30Ni10CoAX > 30Ni10CeAX > 30Ni10LaAX. Experimental results revealed that CO dissociation energy of the catalyst and H2 adsorption ability of the catalyst played a key role in determining the catalytic performance of 30Ni10MAX catalyst in the methanation reaction. Optimal CO dissociation energy of the catalyst and large H2 adsorption ability of the catalyst were favorable for methane production. Among the catalysts tested, 30Ni10FeAX catalyst with the most optimal CO dissociation energy and the largest H2 adsorption ability exhibited the best catalytic performance in terms of conversion of CO and yield for CH4 in the methanation reaction. The enhanced catalytic performance of 30Ni10FeAX was also due to a formation of nickel–iron alloy and a facile reduction. 相似文献