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981.
Seung-Min Oh Hyun-Ha Kim Atsushi Ogata Hisahiro Einaga Shigeru Futamura Dong-Wha Park 《Catalysis Letters》2005,99(1-2):101-104
Toluene was decomposed in a surface discharge plasma reactor packed with various zeolites. The positioning effect of the zeolite bed was also investigated Reactor-B, in which the zeolite bed was located upstream, performed much better than Reactor-A, in which the zeolite bed was located downstream. Furthermore, the decomposition efficiency in Reactor-B increased with the capacity for toluene adsorption on zeolite, while that in Reactor-A did not. The toluene adsorbed in micropores was not decomposed effectively by direct electron impact, but was decomposed by active oxygen species generated in the plasma zone on the zeolite surface. A good correlation was also observed between toluene decomposition and ozone consumption in the downward-type reactor. 相似文献
982.
The different melting temperatures of N‐methyl morpholine N‐oxide (NMMO) hydrates in the cellulose–NMMO hydrate solution may be explained by the rather different crystal structures of NMMO hydrates, which are determined by the amount of the hydrates. The preparative process of cellulose–NMMO hydrate solution may result in cellulose structural change from cellulose I to cellulose II, depending on the amount of the hydrate. Mixtures of cellulose and NMMO hydrate in a blender was changed from the granules to slurry with increasing mixing time at 60–70°C, which is below the melting point of the NMMO hydrate. In the case of 15 wt % cellulose–NMMO hydrate granules, which were made by mixing for 20 min, the melting points of various NMMO hydrates were obtained as 77.8°C (n = 0.83), 70.2°C (n = 0.97), and 69.7°C (n = 1.23), respectively, depending on the hydrate number. However, the melting points of cellulose–NMMO hydrate slurry and solution were shifted lower than those of cellulose granules, while the mixing time of slurry and solution are 25 and 35 min, respectively. These melting behaviors indicate instantaneous liquefaction of the NMMO hydrate and the diffusion of the NMMO hydrate into cellulose during mixing in a blender. When cellulose was completely dissolved in NMMO hydrate, the crystal structure of cellulose showed only cellulose II structure. In the cellulose–NMMO products of granules or slurry obtained by high‐speed mixing, which is a new preparation method, they still retained the original cellulose I structure. © 2004 Wiley Periodicals, Inc. J Appl Polym Sci 93: 1687–1697, 2004 相似文献
983.
984.
Jin-Hae Chang Bong-Ku Choi Jae-Hoon Kim Soo-Min Lee Myung-Sik Bang 《Polymer Engineering and Science》1997,37(9):1564-1571
A thermotropic liquid crystalline polymer (LCP) with an alkyl side-group was synthesized. Blends of the LCP with polycarbonate (PC) were prepared by coprecipitatton from a common solvent. The rheological behavior of the LCP/PC blends was found to be very different from that of PC, and significant viscosity reductions were observed in the temperature range of 200–230°C. Blends of different LCP compositions were extruded with different draw ratio from a capillary rheometer. The ultimate tensile strength showed a maximum at a 10 wt% LCP composition in the blends. It decreased for compositions greater the 10 wt% LCP, whereas the initial modulus increased with increasing LCP content. The morphology of the blends was found to be affected by their compositions. Scanning electron microscopy (SEM) studies revealed finely dispersed spherical LCP domains in the PC matrix. The SEM micrographs also showed a poor adhesion between the two phases. 相似文献
985.
Preparation of three-dimensional ordered macroporous SiCN ceramic using sacrificing template method 总被引:4,自引:0,他引:4
Hao Wang Shuang-yang Zheng Xiao-dong Li Dong-pyo Kim 《Microporous and mesoporous materials》2005,80(1-3):357-362
Three-dimensional (3D) long range well ordered macroporous SiCN ceramics were prepared by infiltrating sacrificial colloidal silica templates with the low molecular weight preceramic polymer, polysilazane. This was followed by a thermal curing step, pyrolysis at 1250 °C in a N2 atmosphere, and finally the removal of the templates by etching with dilute HF. The produced macroporous SiCN ceramics showed high BET surface areas (pore volume) in the range 455 m2/g (0.31 cm3/g)–250 m2/g (0.16 cm3/g) with the pore sizes of 98–578 nm, which could be tailored by controlling the sizes of the sacrificial silica spheres in the range 112–650 nm. The sphere-inversed macropores were interconnected by 50 ± 30 nm windows and 3–5 nm mesopores embedded in the porous SiCN ceramic frameworks, which resulted in a trimodal pore size distribution. The surface of the achieved porous SiCN ceramic was then modified by Pt–Ru nanoparticle depositing under mild chemical conditions. 相似文献
986.
Ji Hye Yoon Sang Beom Choi You Jin Oh Min Jeong Seo Young Ho Jhon Tae-Bum Lee Daejin Kim Seung Hoon Choi Jaheon Kim 《Catalysis Today》2007,120(3-4):324-329
A new mixed-valent iron MOF, formulated as Fe3O(F4BDC)3(H2O)3·(DMF)3.5 (1), has been synthesized by using a perfluorinated linear dicarboxylate to link trigonal prismatic Fe3(μ3-O)(O2C–)6 clusters. The structure refinement based on single crystal X-ray diffraction data collected from 1 reveals the material exhibits the acs topology with large channels along the crystallographic c-axis. Due to the presence of fluorine atoms the organic link, 2,3,5,6-tetrafluorobenzene-1,4-dicarboxylate (F4BDC), has a 63° torsion angle between the carboxylate and aromatic planes, resulting in larger channels compared to those in the isoreticular material MOF-235. While few iron-based MOFs have demonstrated porosity, nitrogen and hydrogen sorption experiments carried out at 77 K proved the porosity of outgassed 1, which has a Langmuir surface are of 635 m2/g and a gravimetric capacity of 0.9 wt% of hydrogen at 1 bar. 相似文献
987.
Copolymerizations of ethylene with 1-decene were carried out with a series of
stereospecific metallocene compounds, rac–(EBI)Zr(NMe2)2 [ 1, EBI = ethylene–1,2–bis( 1–indenyl)], rac–(EBI)Hf(NMe2 (2), rac–Me2Si( 1–C5H2–2–Me–4–
t
Bu)2Zr(NMe2)2
(3), ethylidene(cyclopentadienyl)(9-fluorenyl)ZrMe2 [4, Et(Flu)(Cp)ZrMe2] and isopropylidene(cyclopentadienyl)(9–fluorenyl)ZrMe2 [5, iPr(Flu)(Cp)ZrMe2], combined
with Al(i–Bu)3/[CPh3] [B(C6F5)4] cocatalyst. All catalyst systems showed very high
copolymerization rates and the 1–decene reactivity decreased in the order of 2 > 5 > 1 4 > 3. The reactivity product of ethylene and 1–decene (r
E x r
D) was below 1 except
3 catalyst, corresponding to random copolymer structures with an alternating
character. The melting point (Tm), crystallinity (XC), intrinsic viscosity ([] and
density of the 1–decene/ethylene copolymers decreased markedly with an increase in
the 1–decene content, regardless of the type of catalytic system. 相似文献
988.
Eun-Yong Ko Eun Duck Park Kyung Won Seo Hyun Chul Lee Doohwan Lee Soonho Kim 《Korean Journal of Chemical Engineering》2006,23(2):182-187
Selective CO oxidation in the presence of excess hydrogen was studied over supported Pt catalysts promoted with various transition
metal compounds such as Cr, Mn, Fe, Co, Ni, Cu, Zn, and Zr. CO chemisorption, XRD, TPR, and TPO were conducted to characterize
active catalysts. Among them, Pt-Ni/γ-Al2O3 showed high CO conversions over wide reaction temperatures. For supported Pt-Ni catalysts, Alumina was superior to TiO2 and ZrO2 as a support. The catalytic activity at low temperatures increased with increasing the molar ratio of Ni/Pt. This accompanied
the TPR peak shift to lower temperatures. The optimum molar ratio between Ni and Pt was determined to be 5. This Pt-Ni/γ A12O3 showed no decrease in CO conversion and CO2 selectivity for the selective CO oxidation in the presence of 2 vol% H2O and 20 vol% CO2. The bimetallic phase of Pt-Ni seems to give rise to stable activity with high CO2 selectivity in selective oxidation of CO in H2-rich stream. 相似文献
989.
The removal of hydrogen sulfide (H2S) from simulated gas was carried out in a batch type fluidized-bed reactor using natural manganese ore (NMO), which consists
of several metal oxides (MnOx: 51.85%, FeOy: 3.86%, CaO: 0.11%). The H2S breakthrough curves were obtained by changing temperature, gas velocity, initial H2S concentration, and aspect ratio. Moreover, the effects of the particle size and the particle-mixing fraction on H2S removal were investigated in a binary system of different particle size. From this study, H2S removal efficiency increased with increasing temperature but decreased with increasing excess gas velocity. The breakthrough
time for H2S decreased as the gas velocity increased, which leads to reducing gas-solid contacting due to gas bypassing in a fluidized
bed reactor. Improvement of H2S removal efficiency in continuous process can be expected from the results of the binary particle system with different size
in a batch experiment. The NMO could be considered as a potential sorbent in H2S removal. 相似文献
990.
Native corn starch‐ and hydroxypropylated starch (HPS‐) based plastic films were prepared using the short pulp fiber as the reinforcement and the glycerol as the plasticizer. The results of tensile test showed that the strain and stress at break and elastic modulus increased with pulp content. With glycerol content, the strain at break increased considerably, but the breaking stress and elastic modulus decreased. And the stress–strain curves showed that the brittleness problem of films was overcome by the pulp, glycerol, and water content. The hydroxypropyl starch films showed results similar to those of the native starch films. The results of the three‐point bending test showed that maximum deflection, flexural strength, and specific work increased with pulp content, but the flexural modulus was the highest at a pulp content of 20%. And with the glycerol content, the maximum deflection and specific work of rupture increased, but the bending elastic modulus decreased. The hydroxypropyl starch films showed results similar to those of native starch films as far as the maximum deflection and flexural strength were concerned, but the bending elastic modulus and specific work of the hydroxypropyl starch films were considerably lower than those of starch films. So it was concluded that the flexibility of films was improved by the hydroxypropylation. © 2003 Wiley Periodicals, Inc. J Appl Polym Sci 88: 2108–2117, 2003 相似文献