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991.
Jian Guo Li Fang Jiao HuaTang Yuan Li Qin Wang Hai Xia Li Ming Zhang Yong Mei Wang 《Electrochimica acta》2006,51(28):6275-6280
Layered Li[Ni(1−x)/3Mn(1−x)/3Co(1−x)/3Crx]O2 materials with x = 0, 0.01, 0.02, 0.03, 0.05 are prepared by a solid-state pyrolysis method. The oxide compounds were calcined with various Cr-doped contents, which result in greater difference in morphological (shape, particle size and specific surface area) and the electrochemical (first charge profile, reversible capacity and rate capability) differences. The Li[Ni(1−x)/3Mn(1−x)/3Co(1−x)/3Crx]O2 powders were characterized by means of X-ray diffraction (XRD), charge/discharge cycling, cyclic voltammetry, and SEM. XRD experiment revealed that the Li[Ni(1−x)/3Mn(1−x)/3Co(1−x)/3Crx]O2 (x = 0, 0.01, 0.02, 0.03, 0.05) were crystallized to well layered -NaFeO2 structure. The first specific discharge capacity and coulombic efficiency of the electrode of Cr-doped materials were higher than that of pristine material. When x = 0.02, the sample showed the highest first discharge capacity of 241.9 mAh g−1 at a current density of 30 mA g−1 in the voltage range 2.3–4.6 V, and the Cr-doped samples exhibited higher discharge capacity and better cycleability under medium and high current densities at room temperature. 相似文献
992.
he hydrodynamics and solids mixing behavior in a riser with blunt internals are studied. A uniform radial distribution for solids fraction and particle velocity achieves near the internals. The turbulent velocity of particles near the wall increases with the addition of the internals, with the lateral solids mixing enhanced significantly. Probability density distribution of particle velocity is bimodal in the riser with internals, which is similar to that in the conventional riser, indicating that no significant difference in the micro flow structure exists between the riser with internals and the conventional riser. At the same time, the axial solids mixing behavior changes insignificantly with the addition of internals. These results indicate that the micro flow structure in the riser is very stable, which changes insignificantly with the change of the bed structure. 相似文献
993.
基于表面生物学改性的多孔状二氧化钛/磷灰石复合薄膜的制备 总被引:26,自引:8,他引:26
在钛合金表面采用微孤氧化得到一层多孔状的具有生物活性的二氧化钛,经随后水热处理可形成羟基磷灰石薄膜,提高钛合金表面的生物学性能,用SEM、XRD、EDX分析了薄膜的组织、结构和化学组成,同时考察了微弧氧化得到的二氧化钛膜的生物活性,结果表明,在室温条件下从含钙、磷离子的电解液中在钛合金基体上微弧氧化得到一层二氧化钛薄膜,蒸汽处理后得到具有生物活性的二氧化钛/羟基磷灰石复合薄膜,该膜多孔均匀,且生物活性高,有利于骨组织的吸附和生长。 相似文献
994.
A novel gel-network-coprecipitation process has been developed to prepare ultrafine Cu/ZnO/Al2O3 catalysts for methanol synthesis from CO2 hydrogenation. It is demonstrated that the gel-network-coprecipitation method can allow the preparation of the ultrafine Cu/ZnO/Al2O3 catalysts by homogeneous coprecipitation of the metal nitrate salts in the gel network formed by gelatin solution, which makes the metallic copper in the reduced catalyst exist in much smaller crystallite size and exhibit a much higher metallic copper-specific surface area. The effect of the gel concentration of gelatin on the structure, morphology and catalytic properties of the Cu/ZnO/Al2O3 catalysts for methanol synthesis from hydrogenation of carbon dioxide was investigated. The Cu/ZnO/Al2O3 catalysts prepared by the gel-network-coprecipitation method exhibit a high catalytic activity and selectivity in CO2 hydrogenation to methanol. 相似文献
995.
4,4′‐bis(Phenoxy)diphenyl sulfone (DPODPS) was synthesized by reaction of phenol with bis(4‐chlorophenyl) sulfone in tetramethylene sulfone in the presence of NaOH. Two poly(aryl ether sulfone ether ketone ketone)s (PESKKs) with high molecular weight were prepared by low temperature solution polycondensation of DPODPS and terephthaloyl chloride (TPC) or isophthaloyl chloride (IPC), respectively, in 1,2‐dichloroethane and in the presence of aluminum chloride (AlCl3) and N‐methylpyrrolidone (NMP). The resulting polymers were characterized by various analytical techniques, such as FT‐IR, 1H‐NMR, DSC, TG, and WAXD. The results show that the Tg and Td of PESEKKs are much higher, but its Tm is lower than those of PEKK. The other results indicate that PESEKKs exhibit excellent thermostabilities at 300 ± 10°C. © 2005 Wiley Periodicals, Inc. J Appl Polym Sci 96: 489–493, 2005 相似文献
996.
The mechanical properties and morphological structures of blends based on Zn2+ neutralized low degree sulfated ethylene propylene diene monomer rubber (Zn–SEPDM) ionomer and polypropylene (PP) were studied. It was found that Zn2+ neutralized low degree sulfated EPDM ionomer and PP blends, which are new thermoplastic elastomeric materials, have better mechanical properties than those of PP/EPDM blend. Theoretical analysis of tensile data suggests that there is an increase of the extent of interaction between PP and EPDM in the presence of a low degree of Zn2+, which is also an indicator of better interfacial adhesion between PP and Zn–SEPDM than that between PP and EPDM. SEM results proved that the finer dispersed phase sizes and the shorter interparticle distances are the main reasons for the improved mechanical properties of the PP/EPDM blend. © 2004 Wiley Periodicals, Inc. J Appl Polym Sci 94: 1504–1510, 2004 相似文献
997.
Sang Hern Kim Won Keun Son Yong Joo Kim Eu‐Gene Kang Dong‐Won Kim Chang Woo Park Whan‐Gi Kim Hyung‐Joong Kim 《应用聚合物科学杂志》2003,88(3):595-601
A polystyrene (PS)/poly(butyl acrylate) (PBA) composite emulsion was produced by seeded emulsion polymerization of butyl acrylate (BA) with PS seed particles which were prepared by emulsifier‐free polymerization of styrene with potassium persulfate (KPS) under a nitrogen atmosphere at 70°C for 24 h with stirring at 60 rpm and swelled with the BA monomer in an ethanol/water medium. The structure of the PS/PBA composite particles was confirmed by the presence of the characteristic absorption band attributed to PS and PBA from FTIR spectra. The particles for pure PS and PS/PBA with a low content of the BA monomer were almost spherical and regular. As the BA monomer content was increased, the particle size of the PS/PBA composite particles became larger, and more golf ball‐like particles were produced. The surface morphology of the PS/PBA composite particles was investigated by AFM and SEM. The Tg's attributed to PS and PBA in the PS/PBA composite particles were found at 110 and ?49°C, respectively. The thermal degradation of the pure PS and PS/PBA composite particles occurred in one and two steps, respectively. With an increasing amount of PBA, the initial thermal decomposition temperature increased. On the contrary the residual weight at 450°C decreased with an increasing amount of PBA. © 2003 Wiley Periodicals, Inc. J Appl Polym Sci 88: 595–601, 2003 相似文献
998.
999.
Bo Zhu Jianchun Li Yong He Hideki Yamane Yoshiharu Kimura Haruo Nishida Yoshio Inoue 《应用聚合物科学杂志》2004,91(6):3565-3573
The phase behaviors for the blends of poly(3‐hydroxypropionate) (PHP), poly(L ‐lactide) (PLLA), poly(D ‐lactide) (PDLA), and poly(D,L ‐lactide) (PDLLA) with catechin were investigated by differential scanning calorimetry. In PLLA/catechin, PDLA/catechin, and PDLLA/catechin blends, two glass transitions were detected when the catechin content was ≥40 wt %, whereas in PHP/catechin blends only one glass transition was observed over the whole range of blend compositions. The former and the latter results should reflect the inhomogeneous and the homogeneous nature of the blends, respectively, in the amorphous phase. These different phase behaviors should arise from the differences in the chemical structures between PHP and PLLA/PDLA/PDLLA, which dominates the strength and the number of intermolecular hydrogen‐bonding interactions between the ester carbonyl groups of polyesters and the phenol groups of catechin. As detected by FTIR spectroscopy, in comparison with PHP, the steric hindrance of side‐chain methyl groups of PLLA, PDLA, and PDLLA might restrain the formation of hydrogen bonds between their ester carbonyl groups and the phenol hydroxyl groups of catechin, even weakening the strength of such hydrogen bonds. © 2004 Wiley Periodicals, Inc. J Appl Polym Sci 91: 3565–3573, 2004 相似文献
1000.
Shape‐memory polyurethane/multiwalled carbon nanotube (SMP–MWNT) composites with various multiwalled carbon nanotube (MWNT) contents were synthesized, and the corresponding SMP–MWNT fibers were prepared by melt spinning. The influence of the MWNT content on the spinnability, fracture morphology, thermal and mechanical properties, and shape‐memory behavior of the shape‐memory polymer was studied. The spinning ability of SMP–MWNTs decreased significantly with increasing MWNT content. When the MWNT content reached 8.0 wt %, the fibers could not be produced because of the poor rheological properties of the composites. The melt‐blending, extrusion, and melt‐spinning processes for the shape‐memory fiber (SMF), particularly at low MWNT contents, caused the nanotubes to distribute homogeneously and preferentially align along the drawing direction of the SMF. The crystallization in the SMF was promoted at low MWNT contents because it acted as a nucleation agent. At high MWNT contents, however, the crystallization was hindered because the movement of the polyurethane chains was restricted. The homogeneously distributed and aligned MWNTs preserved the SMF with high tenacity and initial modulus. The recovery ratio and recovery force were also improved because the MWNTs helped to store the internal elastic energy during stretching and fixing. © 2007 Wiley Periodicals, Inc. J Appl Polym Sci, 2007 相似文献