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Xiaohui Wu Jingkang Xu Xingyu Huo Junbo Chen Qin Zhang Fangyi Huang Yuanxun Li Hua Su Lezhong Li 《Journal of the European Ceramic Society》2021,41(10):5193-5200
This work investigates the influence of niobium pentoxide (Nb2O5) as dopant, on the structural, magnetic, and dielectric properties of NiZnCo ferrites. The results showed that Nb2O5 was an effective dopant, and the Nb5+ ions entered the B site to replace Fe3+ ions, which altered the electromagnetic properties of the NiZnCo ferrite. In particular, the coercivity (Hc) was 20~24 Oe, and the magnetic quality factor (Q), was more than 200 at x = 0 and x = 0.1 wt%, which is 4~5 times higher than that of NiZn and NiCuZn ferrites. Excellent electromagnetic properties were obtained for 0.1 wt% Nb2O5-doped NiZnCo ferrite, i.e., Ms = 88.3 emu/g, Hc =20.4 Oe, ρ = 2.4 × 105 Ω m and Q = 202 @20 MHz. These excellent electromagnetic properties of Nb2O5-doped NiZnCo ferrites could be potentially applied to resonators and capacitors at high frequency. 相似文献
25.
Yanqing Zhao Yingli Su Wangcai Zou Gang Chen Yiqing Deng Jun Cheng Haisheng Ren Qiang Zhao 《应用聚合物科学杂志》2021,138(38):50971
In order to prepare waterborne polyurethane with excellent water resistance and thermodynamic properties, a series of side chain fluorinated waterborne polyurethane-urea (FWPU-UA) was synthesized with polytetramethylene ether glycol, N-(2-methyl-1,3-propanediol-2′-)-perfluoro-1-butanesulfonyl amine (NPBA), isophorone diisocyanate, and isophoronediamine. With the increase of NPBA content, the weight loss temperature, glass transition temperature, and tensile strength of FWPU-UA were all improved. Gaussian fitting analysis of infrared data and density functional theory simulation proved that the introduction of fluorine side chains increased the interaction of hydrogen bonding in the FWPU-UA. X-ray photoelectron spectroscopy analysis indicated that the aggregation of fluorine atoms on the surface of film were caused by the migration and enrichment of fluorine side chains. Furthermore, the water resistance of polyurethane-urea film could be significantly improved by adding a small amount of NPBA, and the seven-day water absorption rate of polyurethane-urea film was reduced from 30.13% to 12.55%. 相似文献
26.
Katja F. Hellendahl Felix Kaspar Dr. Xinrui Zhou Zhaoyi Yang Prof. Dr. Zhen Huang Prof. Dr. Peter Neubauer Dr. Anke Kurreck 《Chembiochem : a European journal of chemical biology》2021,22(11):2002-2009
Selenium-modified nucleosides are powerful tools to study the structure and function of nucleic acids and their protein interactions. The widespread application of 2-selenopyrimidine nucleosides is currently limited by low yields in established synthetic routes. Herein, we describe the optimization of the synthesis of 2-Se-uridine and 2-Se-thymidine derivatives by thermostable nucleoside phosphorylases in transglycosylation reactions using natural uridine or thymidine as sugar donors. Reactions were performed at 60 or 80 °C and at pH 9 under hypoxic conditions to improve the solubility and stability of the 2-Se-nucleobases in aqueous media. To optimize the conversion, the reaction equilibria in analytical transglycosylation reactions were studied. The equilibrium constants of phosphorolysis of the 2-Se-pyrimidines were between 5 and 10, and therefore differ by an order of magnitude from the equilibrium constants of any other known case. Hence, the thermodynamic properties of the target nucleosides are inherently unfavorable, and this complicates their synthesis significantly. A tenfold excess of sugar donor was needed to achieve 40−48 % conversion to the target nucleoside. Scale-up of the optimized conditions provided four Se-containing nucleosides in 6–40 % isolated yield, which compares favorably to established chemical routes. 相似文献
27.
《Journal of the European Ceramic Society》2021,41(15):7868-7877
In this work, 0.5TRPO•0.5Gd2Zr2O7 ceramic with an average grain size of only ∼15 nm was prepared by a high pressure (5 GPa/520 °C) sintering method. Phase evolutions and microstructure changes of the as-fabricated super nano and micron-grained ceramics under a high-dose displacement damage induced by 300 keV Kr2+ ions were investigated. The results show that the super nano-grained ceramic has low degree of amorphization, obvious grain growth (2–3 times in grain size) and big Kr bubbles (10–68 nm) formation after irradiation. The micron-grained ceramic was severely amorphized after irradiation and many microcracks were formed parallel to its surface. The formation mechanism of Kr bubbles in the super nano-grained ceramic is on account of grain boundary diffusion and migration induced by the accumulation of the injecting Kr ions and irradiation defects. Nevertheless, microcracks formed in the micron-grained sample are caused by the accumulation of Kr atoms. 相似文献
28.
《Journal of the European Ceramic Society》2021,41(14):6983-6990
Ternary 0.552Pb(Ni1/3Nb2/3)O3-xPbZrO3-(0.448-x)PbTiO3 (PNN-PZ-PT) ceramics near the triple point compositions were fabricated by an improved two-step sintering method. The triple point composition 0.552PNN-0.135PZ-0.313PT ceramic has outstanding piezoelectric performance with piezoelectric coefficient d33 = 1200 pC/N. Its easy fabrication and low cost make this piezoelectric material an excellent candidate for high sensitivity sensors and ultrasonic transducers. The evolution of domain structures for ceramics with composition near the triple point provides deeper insight into the mechanism of ultrahigh piezoelectric properties of PNN-PZ-PT ceramics. 相似文献
29.
微波隔离器是微波系统中不可或缺的器件,常见的隔离器都采用了铁氧体旋磁材料配合吸收负载实现电磁波的单向传输。这种器件虽然可以使电磁波单向传输,但是并不能改善能量的浪费问题,还增加了系统的复杂度。针对上述问题,本文基于电磁超材料设计了一种微波单向传输的圆波导,使用波导内壁涂覆折射率逐渐变化的材料来影响电磁波的传输特性,从而实现电磁波单向传输。本文给出了微波单向传输的电磁计算模型和超材料结构及属性,并通过简化这种超材料使其易于实现;最后通过电磁仿真分析了这种材料的电磁特性并给出了这种材料的实现方法。 相似文献
30.
《Ceramics International》2022,48(10):13719-13731
Li0.04Ca0.96-xSiO3:Smx orange?red emitting phosphors were synthesized using the sol-gel method. X-ray diffraction, Rietveld refinement of XRD patterns, Fourier transform infrared spectroscopy and ?uorescence spectrophotometry were used to characterize the crystal structure, sites of cationic Ca and luminescence properties of the prepared phosphors. The relationship of the different Ca sites in the matrix with the luminescence properties was analysed. The results indicate that the prepared phosphors reveal a β-CaSiO3 phase with a monoclinic crystal structure and space Group P21/a. As the Sm3+ concentration increases, the unit cell volume of phosphors and the Ca–O band lengths of different Ca sites decrease due to substitution of Ca2+ by smaller Sm3+ ions. By excitation at 404 nm, Li0.04Ca0.96-xSiO3:Smx phosphors exhibit warm orange?red light, corresponding to the electron transitions from 4G5/2 → 6H5/2 (567 nm), 4G5/2 → 6H7/2 (605 nm) and 4G5/2 → 6H9/2 (651 nm) of Sm3+. The concentration quenching phenomenon appears at Sm3+ concentrations beyond 0.02. The refinement results demonstrate that three cationic Ca sites, named Ca1, Ca2 and Ca3, exist in the β-CaSiO3 host lattice. The Ca2+ ions at Ca1 and Ca2 sites are coordinated with six oxygen ions, leading to the same coordination number (CN). The Ca2+ ion located at Ca3 site has seven coordination numbers. The Ca1 site possesses a smaller lattice distortion and better symmetry than those of Ca2 and Ca3 sites. However, the Ca3 site exhibits the largest lattice distortion and poor symmetry. The Sm3+ present in symmetric Ca1 sites in the matrix illustrates the strong emission intensity, long luminescence lifetimes and good thermal stability. 相似文献