Investigation of the microwave dielectric properties of the Li4x/3Zn2−2xTi1+2x/3O4 system by P–V–L theory and vibration spectroscopy

Li_4x/3Zn_2–2xTi_1+2x/3O₄ microwave dielectric ceramics with a spinel phase were prepared via a high-temperature solid-phase method. P–V–L theory, vibration spectra, and XPS were utilized to establish the links between the intrinsic and extrinsic factors and the microwave dielectric properties. According to the characterization, the change in permittivity (ε_r) was ascribed to the increase in the average bond ionicity of Ti–O(Af_iTi-O) and the polar mode of the lattice vibration; the change in quality factor(Q × f) resulted from the change in the Ti–O lattice energy (AU_Ti-O) and existence of oxygen vacancy; the increase in temperature coefficient of the resonance frequency (τ_f) was triggered by the increase in the Ti–O bond energy. The Li_0.6Zn_1.1Ti_1.3O₄ ceramics (x = 0.45) sintered at 1125 °C finally obtained optimal microwave dielectric constants of ε_r = 17.3, Q × f = 76,318 GHz and τ_f = -58 ppm/°C.     

Microstructure and some properties of powder-pack borided Ti–5Mo–5V–8Cr–3Al alloy with special attention to the microstructure at the interface TiB/substrate

The borided layer was prepared on the surface of the Ti–5Mo–5V–8Cr–3Al alloy by powder-pack boriding at 1000°C-10h. SEM, EPMA and TEM were used to investigate the effects of alloying elements (Al, V, Mo and Cr) on the growth of TiB whiskers in the borided Ti–5Mo–5V–8Cr–3Al alloy. Wear properties of borided Ti–5Mo–5V–8Cr–3Al alloy were investigated using dry reciprocating friction tests. SEM results show that the thickness of boride layer in Ti–5Mo–5V–8Cr–3Al alloy is thinner than that in the Cp-Ti. This is attributed to the enrichment of alloying elements especially V in TiB/substrate by TEM, which hinders the diffusion of B atoms, thus resulting in the short and thick TiB whiskers in Ti–5Mo–5V–8Cr–3Al alloy. Borided Ti–5Mo–5V–8Cr–3Al alloy has the better wear resistance than as-received alloy.     

退火工艺对激光选区熔化成形Ti6Al4V合金组织及室温力学性能的影响

以Ti6Al4V球形粉末为原料,利用激光选区熔化成形方法制备了Ti6Al4V合金试样,采用光学显微镜、扫描电镜及力学性能测试等手段,研究了退火工艺对Ti6Al4V合金室温力学性能及组织的影响规律。结果表明: SLM成形沉积态Ti6Al4V合金室温抗拉强度超过1200 MPa,而平均断后伸长率仅为4.0%;在650 ℃下进行真空退火处理,合金的抗拉强度仍保持在1200 MPa左右,规定塑性延伸强度R_p0.2高于1150 MPa,但试样的断后伸长率<10%;而在750及800 ℃下进行真空退火处理,合金试样的抗拉强度降至1100 MPa左右,规定塑性延伸强度高于1050 MPa,伸长率达到甚至超过10%,材料的综合强韧性得到明显提升。随着真空退火加热温度和保温时间的增加,SLM成形Ti6Al4V合金原始β晶界逐渐变模糊,晶粒趋向于等轴化。与此同时,快速冷却转变的α′针状马氏体未出现明显地粗化。     

Effect of Different Restorative Materials on Microleakage of Ozone Gas and Traditional Cavity Disinfectant Applied Teeth

The aim of this in vitro study is to investigate the effects of ozone and conventional cavity disinfectant on microleakage at the cavities which are restorated with different restorative materials. Ninety human molar teeth were used in this study. Black V cavities are prepared on buccal surfaces of teeth. Teeth are divided to 3 groups which contains 30 teeth. Group 1: ozone applied; Group 2: 2% chlorhexidine applied; Group 3: any disinfectant is not applied. And then all groups are divided to three subgroups. All subgroups are restored with silorane, ormocer, and traditional composite according to the manufacturer’s directions. Sections were examined under a microscope. Occlusal and gingival microleakage values by a separate researcher and scores were recorded. Statistically results were reviewed with ANOVA and Kruskal–Wallis Tests. Statistically significant difference of microleakage between cavity disinfectant and control groups’ occlusal and gingival lines was not found (p > 0.05). There was no differences at occlusal lines of composite subgroups (p > 0.05) but also significant difference at gingival lines was found (p < 0.05). Statistically significant difference was found among the composite materials, between chlorhexidine and control groups’ gingival lines. The most successful results at gingival lines were found with silorane.     

Investigation on the mechanism of charge generation in organic heterojunctions: Analysis of I–V and C–V characteristics

The charge generation mechanism of organic heterojunction (OHJ) consisted of 1,4,5,8,9,11-hexaazatriphenylene-hexacarbonitrile (HAT-CN) and different hole transporting materials (HTMs) are studied systematically by current-voltage (I–V) and capacitance-voltage measurements. The analysis of I–V characteristics of the devices based on OHJs at forward and reverse voltages by comparing the thickness of HTM layers finds that a forward and reverse symmetrical I–V curve is observed at thin HTM layers and the forward current becomes larger than the reverse current with the increase of HTM thickness, fully illustrating the effectiveness of OHJ charge generation. Moreover, the I–V characteristics at different temperatures indicate that the efficient charge generation is originated from electron tunneling rather than diffusion. And the C–V and capacitance-frequency (C–F)characteristics further illustrate the highly efficient charge generation ability of OHJs so that the charge density is as high as 4.5 × 10¹⁷ cm⁻³, guaranteeing the high conductivity of OHJs, which is very beneficial to developing highly efficient OLEDs using OHJs as charge injector and generator.     

多级深度还原法制备Ti6Al4V合金粉体的基础研究

目前Ti6Al4V合金粉体的生产方法主要有雾化法、机械合金法和氢化脱氢法,它们都以Kroll法生产海绵钛为基础。使用钛的氧化物作为原料的熔盐电解法和金属热还原法仍处于研究阶段。本文依据变价金属Ti和V的氧化物在还原过程中逐级还原的特性,提出使用金属氧化物(TiO₂, V₂O₅)作为原料的多级深度还原法制备Ti6Al4V合金粉体的新思路。首先计算了TiO₂-V₂O₅-Mg-Ca体系的吉布斯自由能变,结果表明先进行镁热自蔓延反应,后进行钙热深度还原反应制备Ti6Al4V合金粉体在热力学上具备可行性。然后通过实验进行了的验证。镁热自蔓延反应产物酸浸后除去MgO可得到氧含量为15.84%的多孔Ti-Al-V-O前驱体。配入金属Ca后进行深度脱氧可得到低氧Ti6Al4V合金粉体(Al: 6.2wt.%, V: 3.64wt.%, O: 0.24wt.%, Mg: 0.01wt.%, Ca: < 0.01wt.%)。     

Reaction between methanol and acetic acid catalyzed by SiO2‐supported V‐P‐O catalyst in oxygen atmosphere

SiO₂‐supported V‐P‐O catalysts prepared by the incipient‐wetness impregnation method beginning with ammonium metavanadate and phosphoric acid were used in the catalytic reaction between methanol and acetic acid in an oxygen atmosphere. The SiO₂‐supported V‐P‐O catalysts were composed of VOPO₄ and (VO)₂P₂O₇ phases. Both the acidic and alkaline sites were co‐present in the catalysts. The vanadium species catalyzed the oxidation of methanol to formaldehyde. The V‐P‐O(20–30 wt%)/SiO₂ catalysts with a P/V mole ratio of 2:1 exhibited higher catalytic activity for the formation of acrylic acid and methyl acrylate with a total selectivity of ～28 % at 380 °C. The acid sites of the catalysts also catalyzed the formation of methyl acetate with a selectivity of ～65 %. Methanol can be an alternative to formaldehyde for the synthesis of both acrylic acid and methyl acrylate through the aldol condensation reaction.     

柴油加氢装置掺炼沸腾床渣油加氢柴油馏分生产国Ⅴ柴油可行性研究

进行了柴油加氢装置掺炼沸腾床渣油加氢装置生产的柴油馏分(简称沸腾床加氢柴油),生产满足GB19147—2016车用柴油(Ⅴ)标准(国Ⅴ车用柴油标准)柴油的可行性研究。结果表明,常规柴油加氢装置掺炼一定比例的沸腾床加氢柴油馏分,可以生产出国Ⅴ车用柴油调合组分;直馏柴油掺炼30%沸腾床加氢柴油,在反应压力6.5MPa、体积空速1.5h~(-1)、反应温度360℃、氢油体积比500的条件下,精制柴油满足国Ⅴ车用柴油标准;混合柴油(直馏柴油、焦化柴油和催化裂化柴油的质量比为62∶25∶13)掺炼30%沸腾床加氢柴油,在反应压力7.3 MPa、体积空速1.0h~(-1)、反应温度355℃、氢油体积比500的条件下,可以生产出硫含量满足国Ⅴ标准的车用柴油调合组分。本研究结果可为沸腾床加氢柴油馏分的加工路线提供理论依据。     

ETSI EN 301893 V2.1.1中自适应测试方法及要点

介绍了ETSI EN 301893 V2.1.1:2017中的新增自适应测试参数,该测试是5G WiFi测试中的一个难点。通过对测试中遇到的常见问题及测试结果分析,指出了测试中需要注意的测试环境搭建细节。     

多孔石墨烯/碳纳米管@V2O5柔性电极材料制备及性能研究

以氧化石墨、碳纳米管、三异丙氧基氧化钒为原料,采用化学刻蚀法、水热法、真空抽滤法制备一种具有三维离子扩散通道和整体导电网络结构的致密多孔石墨烯/碳纳米管@五氧化二钒(PGNs/CNT@V2O5)复合薄膜材料。电化学性能测试结果表明,在1 mol/L LiNO3水系条件中,电流密度为1 A/g时,比容量高达187 F/g,在100 mV/s扫描速度下,循环5000次后,容量保持率仍为83.4%。