TiB2 powders were synthesized by borothermal reduction in nanoscale TiO2 with boron under vacuum. Reaction processes were investigated, and the effect of by‐product B2O3 was evaluated. Results showed that TiO2 was firstly reduced by boron to form TiBO3 and Ti2O3, and then to produce TiB2 and B2O3 with increasing temperature. The reaction processes of TiB2 powders synthesis included two‐step reduction in TiO2 by boron and the removal of B2O3. The presence of B2O3, which was previously reported as the most important factor in promoting the coarsening of ZrB2 and HfB2 powders by borothermal reduction, did not lead to significant coarsening of TiB2 powders. Due to the minor effect of B2O3, TiB2 powders with small particle size and low oxygen content could be prepared by direct heat treatment of TiO2 and boron at 1550°C under vacuum for 1 h. The particle size and oxygen content of synthesized TiB2 powders were ~0.9 μm and ~1.7 wt%, respectively. 相似文献
Ag2MoO4 ceramic was prepared by using the solid‐state reaction method, which could be sintered at 450°C for 2 h, having a relative permittivity of 8.08, a Qf value of 17 000 GHz, and a temperature coefficient of resonance frequency about ?133 ppm/°C. Ag2MoO4 ceramic was chemically compatible with silver but reacted seriously with aluminum to form (Ag0.5Al0.5)MoO4 during the sintering. The fitting of infrared spectra and the Shannon's additive rule were employed to study intrinsic dielectric behaviors of the ceramics at microwave region. Ionic displacive polarization and the electronic polarization contributed almost equally to the dielectric permittivity of the ceramic at microwave region. The Ag2MoO4 ceramics could be a good candidate for ultra‐low temperature co‐fired microwave devices. 相似文献
以两种人工钠化膨润土为研究对象,探讨了文献胶质价测试方法的不合理性、取土量和MgO量这两个关键因素。实验结果表明:用常规100 mL量筒测胶质价时,取土量和MgO量影响较大,有必要针对具体试样做条件试验,最佳条件是1#钠土为取3.00 g土、0.2 g MgO,2#钠土为取5.00 g土、0.33 g MgO。 相似文献
This study focuses on the effects of the tetrahydrofuran-soluble fraction of direct coal liquefaction residue as a modifier to modify asphalt with formaldehyde. The properties and carbonization behavior of matrix asphalt and the modified asphalts were studied. The results indicate that the ductility properties of modified asphalts have been effectively improved. The morphology of modified asphalts without the addition of formaldehyde is a set of uniform distribution point, and it is converted from linear distribution to clustered distribution observed in fluorescence microscope images with the increase of the adding amount of formaldehyde. 相似文献
By using Cinchona‐derived chiral phosphines as catalytic ligands, enantioenriched cis‐3a,8a‐hexahydropyrrolo[2,3‐b]indoles (ent‐HPIs), which are core scaffolds in a large array of biologically active natural products, can be convergently assembled under mild conditions through the silver(I)‐catalyzed asymmetric domino reaction of readily available isocyanoacetates and 2‐(2‐aminophenyl)acrylates. Various functionalities can be tolerated in the reaction, affording enantioenriched HPIs in high overall yields and good enantioselectivities (up to 92% ees).
Dynamic reductive kinetic resolutions of racemic 3‐arylalkanones have been performed by the proper combination of an alcohol dehydrogenase and a basic anionic resin. The best results were found for the bioreduction with the alcohol dehydrogenase type A from Rhodococcus ruber DSM 44541 overexpressed in Escherichia coli (E. coli/ADH‐A) and the commercially available evo‐1.1.200, while the Amberlite IRA‐440 C and the DOWEX‐MWA‐1 resins allowed efficient in situ racemizations. Reaction conditions were optimized in terms of enzyme source and loading, type and amount of resin, pH, temperature and reaction times, obtaining a series of (R,R)‐substituted propan‐2‐ols with good conversions and both diastereoselectivity and stereoselectivity. As a proof of concept, the subsequent intramolecular cyclization of a selected propan‐2‐ol substrate afforded a valuable isochroman heterocycle without any loss of the optical purity.
Copper‐catalyzed aerobic coupling of thiols and alcohols affords sulfinates and thiosulfonates. These products are assumed to form via sulfinyl radicals which are not commonly found in oxidative coupling reactions of thiols. A reaction mechanism involving sulfinyl radicals is proposed, and mass and electron paramagnetic resonance (EPR) experimental results are provided.