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81.
Baik Joon Hyun Yim Sung Dae Nam In-Sik Mok Young Sun Lee Jong-Hwan Cho Byong K. Oh Se H. 《Topics in Catalysis》2004,30(1-4):37-41
Topics in Catalysis - Among the catalysts screened, Cu-ion exchanged ZSM5 zeolite exhibited the highest NO removal activity, particularly at low reaction temperatures below 200 °C,... 相似文献
82.
The poly(vinyl alcohol) (PVOH) is an eco‐friend polymer and has an excellent oxygen barrier property due to its strong intermolecular force, but difficulty in processing with conventional extrusion process gives it a limitation for various industrial applications, especially packaging industry. Many studies have attempted to plasticize PVOH to improve its processability, but high cost of PVOH is still drawback for a variety of industrial applications. Therefore, PVOH often blended with other biodegradable polymers such as starch to acquire the cost benefit. Nowadays, the butenediol vinyl alcohol copolymer (BVOH) is getting a great attention due to its melt processability and bio‐degradability, but its high cost is barrier to the industrial application as well. In this study, thermoplastic starch (TPS)/plasticized BVOH (P‐BVOH) were prepared by melt mixing technique, and the plasticization effect of glycerol on starch and BVOH with different composition was observed for optimized processing condition. Based on our preliminary study, TPS was blended with varying amount of P‐BVOH (100:0, 90:10, 80:20, 70:30, 60:40, and 50:50 weight ratio). Physical, oxygen barrier, and mechanical properties of the TPS/P‐BVOH blends were evaluated by various analytical instruments to achieve balanced property and performance. J. VINYL ADDIT. TECHNOL., 25:109–116, 2019. © 2018 Society of Plastics Engineers 相似文献
83.
X.?J.?Wang Y.?N.?Zhou H.?S.?Lee K.?W.?Nam X.?Q.?Yang O.?HaasEmail author 《Journal of Applied Electrochemistry》2011,41(2):241-247
1 M LiPF6 dissolved in oligo(ethylene glycol) dimethyl ether with a molecular weight, 500 g mol−1 (OEGDME500, 1 M LiPF6), was investigated as an electrolyte in experimental Al–Li/LiFePO4 cells. More than 60 cycles were achieved using this electrolyte in a Li-ion cell with an Al–Li alloy as an anode sandwiched
between two Li
x
FePO4 electrodes (cathodes). Charging efficiencies of 96–100% and energy efficiencies of 86–89% were maintained during 60 cycles
at low current densities. A theoretical investigation revealed that the specific energy can be increased up to 15% if conventional
LiC6 anodes are replaced by Al–Li alloy electrodes. The specific energy and the energy density were calculated as a function of
the active mass per electrode surface (charge density). The results reveal that for a charge density of 4 mAh cm−2 about 160 mWh g−1 can be reached with Al–Li/LiFePO4 batteries. Power limiting diffusion processes are discussed, and the power capability of Al–Li/LiFePO4 cells was experimentally evaluated using conventional electrolytes. 相似文献
84.
85.
In this work, we studied the characteristic variations of catalyst supports caused by mechanical milling and their electrochemical application in fuel cells. Two different catalyst supports, carbon black (XC-72R) and K20 (mesoporous carbon), were crushed and dispersed by mechanical milling using a bead mill. The bead mill operated with 0.3 μm zirconia beads at the rate of 3500 rpm for 30 min. The secondary particle size of the crushed catalyst supports ranged from around 0.1 μm to 10 μm. The secondary particle size of the catalyst supports after crushing represents a decrease of approximately 10% compared with that of raw catalyst supports. To confirm the role of the catalyst supports in the direct methanol fuel cell (DMFC), Pt and Ru were loaded onto these catalyst supports using an impregnation method. In the single cell test, Pt-Ru/XC-Bead and PtRu/K20-Bead showed power densities of 135 mW/cm2 and 144 mW/cm2 under air at 60 °C, respectively. The performance values of these catalysts, which were fabricated using reformed catalyst supports, were 10% to 20% higher than those of raw catalyst supports. As a result, the catalyst supports crushed by the bead mill helped to improve the electrochemical performance of the direct methanol fuel cell. 相似文献
86.
Jin Woo Bae Tae Uk Yang Gi Joon Nam Gun Joo Lee Byeong-Uk Nam Jae Young Jho 《Polymer Bulletin》2011,67(4):729-740
Ethylene vinylacetate (EVA) copolymer-based nanocomposites with maleic anhydride-grafted ethylene-vinylacetate (EVAgMA) and
organically modified clay (o-clay) were prepared in a twin screw extruder by following a two-step melt compounding method.
EVAgMA/o-clay masterbatches with various clay contents up to 50 wt% were examined, after which the masterbatch with the highest
clay content was melt compounded with EVA for the preparation of EVA/o-clay nanocomposites containing specific amounts of
clay. Further morphological dispersion of the clay particles by highly polar EVA and shearing was confirmed in the EVA/o-clay
nanocomposites by X-ray diffraction (XRD) and transmission electron microscopy (TEM). These morphologies led to increased
thermal properties in air as well as a considerable decrease in heat release rate (HRR). EVA/o-clay/MDH nanocomposites were
also prepared using a high clay-bearing masterbatch to confirm the synergistic flame retardancy of clay as a co-additive in
EVA/MDH composites. EVA/o-clay/MDH nanocomposites prepared by substituting o-clay for MDH showed significantly lower and wider
HRR during combustion compared to EVA/MDH composite. 相似文献
87.
Ho Chul Shin Kyung Wan Nam Won Young Chang Byung Won Cho Won-Sub Yoon Xiao-Qing Yang Kyung Yoon Chung 《Electrochimica acta》2011,(3):1182
The structural changes of LiFePO4 and C-coated LiFePO4 during charging at various C-rates and temperatures are investigated using synchrotron based in situ X-ray diffraction technique. The XRD patterns collected during cycling show the structural evidence of the positive effects of carbon coating on LiFePO4 for the electrochemical performance improvements at different temperatures, especially at low temperatures. At −10 °C, the C-coated LiFePO4 shows comparable capacities with the sample cycled at room temperature when cycled at C/5 rate with a slight shift of the plateau to a higher voltage during charging. The in situ XRD patterns collected simultaneously show a complete phase transformation from triphylite to heterosite. At −20 °C, the C-coated LiFePO4 delivers 55.6% of its theoretical capacities at C/5 rate. However, the plateau in the charging curve becomes sloppy and shifts to a higher voltage. The in situ XRD patterns show that the phase transformation from triphylite to heterosite is not completed when charged to 4.5 V due to the larger polarization when charged at −20 °C. 相似文献
88.
Sunhyung Kim Jonghee Han Yongchai Kwon Kug-Seung Lee Tae-Hoon Lim Suk Woo Nam Jong Hyun Jang 《Electrochimica acta》2011,(23):7984
Using platinum (Pt) black and carbon-supported Pt (Pt/C) as cathode catalysts, membrane-electrode assemblies (MEAs) were fabricated with various Nafion ionomer content, and their direct formic acid fuel cell (DFAFC) performances were investigated. In MEAs incorporating Pt black catalysts, the current density at 0.6 V was highest at ionomer/catalyst volume ratio of 1.0, which was consistent with the electrochemical active area (EAS) variation measured by cyclic voltammetry. However, the current density measured at 0.3 V, the cell performance increased with Nafion ionomer content, especially at low ionomer loading, indicating that proton transport rate played an important role. The variation in ionic resistance (Rion) of cathode layers with Nafion ionomer content was experimentally confirmed by using the complex capacitance analysis of impedance data implemented with nitrogen (cathodes)/hydrogen (anodes) atmosphere. For Pt/C, the layer thickness and EAS of cathode were larger than those of MEA cathode using Pt black; and the current densities at 0.6 V were lower than those of Pt black, suggesting that smaller fraction of EAS was utilized. 相似文献
89.
Jae Hee Jung Sun Young Park Jung Eun Lee Chu Won Nho Byung Uk Lee Gwi Nam Bae 《Journal of aerosol science》2011,42(10):725-736
Aerosol techniques have recently been used to process natural products for medical, pharmaceutical, and environmental health applications. In particular, electrohydrodynamic spraying, or electrospraying, which is a method of atomizing liquids by means of electrical forces, is a promising aerosol technology because it generates non-agglomerated particles due to repulsive electrical forces between particles with unipolar charges. We investigated the characteristics of natural-product nanoparticles generated via electrospraying. A plant extract containing a natural-product (Sophora flavescens) was sprayed in steady cone-jet mode using a specially designed electrospray system with a point-to-orifice-plate configuration. The electrosprayed natural-product particles maintained their bimodal size distribution with good stability and uniformity for longer than 1 h. Compared to generation characteristics observed using a conventional nebulization process, the electrospray technique produced non-agglomerated, spherical particles and resulted in a narrow size range for both peaks. The size distribution of electrosprayed particles was controlled by varying the suspension flow rate of S. flavescens extract. Also, they had a high average charge per particle and positive polarity. The nanoparticles maintained the major chemical composition of the original S. flavescens ethanolic extract during electrospraying. Our investigation demonstrated that the electrospray process, driven by high-intensity electric fields, can be used to generate nanoscale particles from natural products. 相似文献
90.
Ten selected samples with varying types and amounts of organic matter from two Miocene lacustrine basins in northwestern Turkey were analyzed by programmed-temperature open-system pyrolysis to determine methane generation potential and reaction kinetics. Open-system pyrolysis was performed at heating rates 0.1, 0.7 and 5.0 K/min, where generated gases were measured using an on-line gas chromatograph. Frequency factors and activation energy distributions of reaction kinetics for methane generation from the investigated lacustrine coals and sedimentary rocks indicated that type of kerogen controls the sequential order of methane generation. Methane from Type-III kerogen is generated at lower temperatures, which will be followed by methane from Type-II and Type-I kerogen. Methane generation potentials in the range 14-35 mg CH4/g TOC correlates also with type of organic matter. For Type-III kerogen up to 28% of the total hydrocarbon generation potential belongs to methane. The respective value is only 2% for a Type-I kerogen. 相似文献