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131.
LiCoO2 xerogel hollow nanofibers were first prepared by co‐electrospinning the sol precursor, and the polycrystalline LiCoO2 hollow nanofibers were obtained after calcination of the xerogel fibers. The obtained hollow nanofibers made up of 20~30 nm nanocrystals were about 100 nm to several micrometers in outer diameter. The hollow nanofibers were detected by means of SEM, TEM, TG, DSC, FTIR, and XRD techniques. 相似文献
132.
Using a coaxial capillary spinneret electrospinning technique combined with the sol-gel method, the nickelic xerogel hollow nanofibers first were prepared and the polycrystalline LiNiO2 hollow nanofibers were obtained after sintering. The obtained hollow nanofibers were about 500 nm to 4 µm in outer diameter, and were made up of 20 ~ 30 nm nanocrystals. The xerogel hollow nanofibers and those calcined at different temperatures were characterized by thermogravimetric (TG) analysis, Fourier transform infrared (FTIR) spectrum, x-ray diffractometry (XRD), transmission electron microscopy (TEM), and scanning electron microscopy (SEM). 相似文献
133.
微米及纳米丝光沸石分子筛上二甲醚羰基化反应的积碳分析 总被引:1,自引:0,他引:1
对比研究了在传统微米尺寸和新结构纳米丝光沸石催化剂上二甲醚羰基化合成乙酸甲酯的反应行为.结果表明,通过减小分子筛的尺寸到纳米水平,可以有效提高反应物和产物到达或者脱离反应活性位的效率,从而提高了二甲醚的转化率;更重要的是,抑制了硬积碳的生成,使催化剂保持了更高的稳定性. 相似文献
134.
Biodegradable poly(butylene succinate) (PBS) and layered double hydroxide (LDH) nanocomposites were prepared via melt blending in a twin-screw extruder. The morphology and dispersion of LDH nanoparticles within PBS matrix were characterized by transmission electron microscopy (TEM), which showed that LDH nanoparticles were found to be well distributed at the nanometer level. The nonisothermal crystallization behavior of nanocomposites was extensively studied using differential scanning calorimetry (DSC) technique at various cooling rates. The crystallization rate of PBS was accelerated by the addition of LDH due to its heterogeneous nucleation effect; however, the crystallization mechanism and crystal structure of PBS remained almost unchanged. In kinetics analysis of nonisothermal crystallization, the Ozawa approach failed to describe the crystallization behavior of PBS/LDH nanocomposites, whereas both the modified Avrami model and the Mo method well represented the crystallization behavior of nanocomposites. The effective activation energy was estimated as a function of the relative degree of crystallinity using the isoconversional analysis. The subsequent melting behavior of PBS and PBS/LDH nanocomposites was observed to be dependent on the cooling rate. The POM showed that the small and less perfect crystals were formed in nanocomposites. 相似文献
135.
136.
Dr. Hui Cai Zhan‐Yi Sun Zhi‐Hua Huang Lei Shi Prof. Dr. Yu‐Fen Zhao Prof. Dr. Horst Kunz Prof. Dr. Yan‐Mei Li 《Chemistry (Weinheim an der Bergstrasse, Germany)》2013,19(6):1962-1970
Glycopeptides of tumor‐associated mucin MUC1 are promising target structures for the development of antitumor vaccines. Because these endogenous structures were weakly immunogenic, they were coupled to immune‐response‐stimulating T‐cell epitopes and the Pam3Cys lipopeptide to induce strong immune responses in mice. A new thioether‐ligation method for the synthesis of two‐ and three‐component vaccines that contain MUC1 glycopeptides as the B‐cell epitopes, a T‐cell epitope peptide, and the Pam3CSK4 lipopeptide is described. The resulting fully synthetic vaccines were used for the vaccination of mice, either in a liposome with Freund′s adjuvant or in aqueous PBS buffer. The three‐component vaccines that contained the Tetanus Toxoid P2 T‐cell epitope peptide induced strong immune responses, even when administered just in PBS. By activation of the complement‐dependent cytotoxicity (CDC) complex, the antisera induced the killing of tumor cells. 相似文献
137.
Yihao Luan Jin Wu Maosheng Zhan Jinming Zhang Jun Zhang Jiasong He 《Cellulose (London, England)》2013,20(1):327-337
Using native cellulose as the starting material, cellulose acetate-graft-ploy (l-lactide) (CA-g-PLA) copolymers were successfully synthesized by “one-pot” process in an ionic liquid 1-allyl-3-methylimidazolium chloride (AmimCl). In this process, cellulose was first reacted with acetic anhydride, yielding cellulose acetate (CA), and then ring opening graft copolymerization of l-lactide was carried out from the residual hydroxyl groups of CA in the same solution using 4-dimethylaminopridine (DMAP) as the catalyst. Both acetyl and ploy (l-lactide) contents in CA-g-PLA copolymers could be well controlled by changing reaction conditions. The structures and thermal properties of CA-g-PLA copolymers were characterized. The glass transition temperature Tg of copolymers decreased with increasing PLA content. Compared to the pure PLA and cellulose-graft-PLA copolymers, the CA-g-PLA copolymers possessed better thermo mechanical properties in a temperature range of 60–130 °C. When the molar substitution of PLA (MSPLA) was above 1.71, the CA-g-PLA copolymers exhibited thermoplastic behavior and could be processed by conventional thermal processing methods, such as injection molding and melt spinning. 相似文献
138.
Dapeng Zhan 《Probability Theory and Related Fields》2015,161(3-4):561-618
139.
Qing‐Hui Guo Zhan‐Da Fu Liang Zhao Mei‐Xiang Wang 《Angewandte Chemie (Weinheim an der Bergstrasse, Germany)》2014,126(49):13766-13770
O6‐Corona[3]arene[3]tetraazines, a new class of macrocyclic compounds, were synthesized efficiently in a one‐pot reaction from the nucleophilic aromatic substitution reaction between 1,4‐dihydroxybenzene derivatives and 3,6‐dichlorotetrazine in warm acetonitrile. In the crystalline structure, the resulting macrocycles adopt highly symmetric structures of a regular hexagonal cavity with all bridging oxygen atoms and tetrazine rings located on the same plane with phenylene units orthogonally orientated. The constitutional aromatic rings are able to rotate around the macrocyclic annulus, depending on the steric effect of the substituents and temperature, in solution. The electron‐deficient nature revealed by cyclic voltammetry, differential pulse voltammetry, and characteristic absorbances at a visible region show the O6‐corona[3]arene[3]tetrazines to be suitable macrocyclic receptors for electron‐rich guests. 相似文献
140.
Multi‐walled carbon nanotube modified dummy‐template magnetic molecularly imprinted microspheres as solid‐phase extraction material for the determination of polychlorinated biphenyls in fish 下载免费PDF全文
Ning Gan Xidong Chen Yuting Cao Tianhua Li Pan Zhan 《Journal of separation science》2014,37(13):1591-1600
Novel multi‐walled carbon nanotube modified dummy‐template molecularly imprinted microspheres (MWCNTs@DMMIPs) were successfully synthesized as adsorbents for six kinds of polychlorinated biphenyls (PCBs). MWCNTs@DMMIPs were prepared by a surface molecular imprinting technique. Core–shell Fe3O4@SiO2 nanoparticles were employed as magnetic support. 3,4‐Dichlorobenzene acetic acid was used as a dummy template instead of PCBs, methacrylic acid was used as functional monomer and ethylene glycol dimethacrylate was used as the cross‐linker. The resulting absorbent was characterized by various methods. The adsorbent was employed for extracting PCBs and exhibited good selectivity and high adsorption efficiency. Furthermore, it was reusable and capable of magnetic separation. Adsorption kinetics fit well with a pseudo‐second‐order kinetic equation and also exhibited a three‐stage intra‐particle diffusion model. The Freundlich model was used to describe the adsorption isotherms. The materials were successfully applied to the magnetic dispersive solid‐phase extraction of six kinds of PCBs followed by gas chromatography with mass spectrometry determination in fish samples, the limit of detection of six kinds of PCBs were 0.0028–0.0068 μg/L and spiked recoveries ranged between 73.41 and 114.21%. The prepared adsorbent was expected to be a new material for the removal and recovery of PCBs from contaminated foods. 相似文献