循环流化床锅炉快速床流体动力学结构研究

论述了快速床区流体动力学的结构，研究了快速床区纵向和横向悬浮密度分布的规律及相应的计算公式。对影响快速床区动力学结构的主要因素，如固体颗粒的循环率、气体速度等进行了试验研究，对循环流化床锅炉的设计和运行有一定的指导意义。     

一元弱酸表观离解常数pKa的测定

本文依据Ｈｅｌｍｋａｍｐ和Ｊｏｈｎｓｏｎ所提出的实验方法，通过选择易溶于水的弱酸，采用电位滴定法准确测定滴定ＨＡ至一半时溶液的氢离子浓度，得到表观离解常烤ｐＫａ，并通过数学方法计算出经对ｐＫａ，该方法不仅能用于ｐＫａ〈１１．３弱酸，也可以用于ｐＫａ≥１１．３的极弱酸离解常数的测定，具有简单，快速，准确的特点。     

Composition-dependent xBa(Zr0.2Ti0.8)O3-(1-x)(Ba0.7Ca0.3)TiO3 bulk ceramics for high energy storage applications

This work reports the composition dependent microstructure, dielectric, ferroelectric and energy storage properties, and the phase transitions sequence of lead free xBa(Zr_0.2Ti_0.8)O₃-(1-x)(Ba_0.7Ca_0.3)TiO₃ [xBZT-(1-x)BCT] ceramics, with x?=?0.4, 0.5 and 0.6, prepared by solid state reaction method. The XRD and Raman scattering results confirm the coexistence of rhombohedral and tetragonal phases at room temperature (RT). The temperature dependence of Raman scattering spectra, dielectric permittivity and polarization points a first phase transition from ferroelectric rhombohedral phase to ferroelectric tetragonal phase at a temperature (T_R-T) of 40?°C and a second phase transition from ferroelectric tetragonal phase - paraelectric pseudocubic phase at a temperature (T_T-C) of 110?°C. The dielectric analysis suggests that the phase transition at T_T-C is of diffusive type and the BZT-BCT ceramics are a relaxor type ferroelectric materials. The composition induced variation in the temperature dependence of dielectric losses was correlated with full width half maxima (FWHM) of A₁, E(LO) Raman mode. The saturation polarization (P_s) ≈8.3?μC/cm² and coercive fields ≈2.9?kV/cm were found to be optimum at composition x?=?0.6 and is attributed to grain size effect. It is also shown that BZT-BCT ceramics exhibit a fatigue free response up to 10⁵ cycles. The effect of a.c. electric field amplitude and temperature on energy storage density and storage efficiency is also discussed. The presence of high T_T-C (110?°C), a high dielectric constant (ε_r ≈?12,285) with low dielectric loss (0.03), good polarization (P_s ≈?8.3?μC/cm²) and large recoverable energy density (W?=?121?mJ/cm³) with an energy storage efficiency (η) of 70% at an electric field of 25?kV/cm in 0.6BZT-0.4BCT ceramics make them suitable candidates for energy storage capacitor applications.     

高密度聚乙烯导电复合材料介电性能的研究

用熔融共混和热压工艺制备了CB/HDPE,MWNT/HDPE聚合物基复合材料,研究了填料体积含量,测试电压,填料形貌尺寸对复合体系介电性能的影响.实验表明,当导电填料含量达到渗流阈值附近时复合材料的介电常数达到最大,测试电压达到一定值时,渗流阈值附近的复合材料介电损耗会迅速增加,相同填料体积含量的MWNT/HDPE复合体系比CB/HDPE体系具有更高的介电常数,利用渗流理论、Maxwell-Wagner界面极化效应和微电容模型解释了实验现象.     

常压液相法一步合成铌掺杂二氧化钛

采用四氯化钛为钛源,常压下在离子液体（1-乙基-3-甲基咪唑四氟化硼酸盐）中一步合成掺杂铌的二氧化钛粉末。采用X射线衍射、扫描电子显微镜、紫外–可见漫反射光谱对产物的结晶、掺杂、表面形貌进行表征,并测试了掺杂量的改变对光吸收性及表观介电常数的影响。结果表明：制备的掺杂TiO2粉末为锐钛矿晶型且结晶完善;Nb5＋掺杂使粉末光吸收带边发生蓝移;掺杂后粉末的介电常数增大,当掺杂Nb量为5%（摩尔分数）时表观介电常数达到最高值。     

铬酸酐掺杂V2O5制备高红外反射率氧化铬绿颜料

研究了铬酸酐热分解制备高性能红外反射氧化铬绿颜料,在优化现有铬酸酐热分解工艺的基础上,详细探讨了掺杂制备红外反射氧化铬绿颜料的工艺条件和相关机理。借助UV-vis-NIR、FT-IR、SEM、XRD和CIE-L^*a^*b^*等手段发现:在铬酸酐热分解过程中,不同的热分解温度导致粒径变化,从而影响红外反射率;优化的制备工艺条件(热分解温度1250℃、热分解时间0.5 h)下,氧化铬绿的红外反射率达到90%。在掺杂过程中,V₂O₅的添加可使氧化铬绿的最高红外反射率达到98%。随着V₂O₅添加量的增加,红外反射率先增加后减少;当V/Cr摩尔比为0.004时,红外反射率、电导率、介电常数都达到极值,三者呈现一致的规律性变化。初步机理探索表明,氧化铬本征导电类型为空穴导电,掺杂V₂O₅以后导电类型发生改变,伴随着电阻率的变化,氧化铬吸收和反射光子能力改变,从而影响红外反射性能。     

硫酸盐对聚羧酸减水剂吸附量及吸附动力学的影响

在研究聚羧酸减水剂在水泥颗粒表面的吸附量、吸附速率的基础上,运用不同吸附动力学模型对试验结果进行拟合。吸附量测试结果表明:掺0.5%、1.0%Na2SO4会显著降低聚羧酸减水剂在水泥颗粒表面的吸附量,但掺0.1%、0.2%的Na2SO4有利于聚羧酸减水剂的吸附;CaSO4·2H2O对聚羧酸减水剂的吸附量影响不显著。吸附速率测试及拟合结果表明:硫酸盐对聚羧酸减水剂在水泥颗粒表面吸附动力学的影响规律符合Langmuir准二级吸附动力学模型,Na2SO4通过改变聚羧酸减水剂在水泥颗粒表面的准二级吸附速率常数影响聚羧酸减水剂吸附达到平衡的时间,0.2%、1.0%掺量的Na2SO4均延迟了聚羧酸减水剂达到吸附平衡的时间。掺0.2%Na2SO4使准二级吸附速率常数较不掺硫酸盐时有所提高;掺1.0%Na2SO4的准二级吸附速率常数较不掺硫酸盐时大大降低;CaSO4·2H2O对准二级吸附速率常数的影响较Na2SO4要小。     

微波技术在压电陶瓷材料中的研究进展及应用前景

本文简要介绍了微波水热和微波烧结技术的作用机理和特点,综述了微波水热与微波烧结在制备压电陶瓷方面的研究进展。在合成压电陶瓷材料上的应用上对微波制备技术与传统工艺进行比较,表明微波制备技术是一种极具潜力的技术;最后对微波水热结合微波烧结技术在提高压电陶瓷性能方面的前景作了展望并提出微波制备工艺在未来发展中亟待解决的若干问题。     

Synthesis of highly soluble and transparent polyimides

A novel aromatic diamine, 3,3′‐diisopropyl‐4,4′‐diaminophenyl‐4″‐methyltoluene with a 4‐methylphenyl pendant group and isopropyl side groups, was designed and synthesized in this study. Then it was polymerized with various aromatic dianhydrides including pyromellitic dianhydride, 3,3′,4,4′‐biphenyltetracarboxylic dianhydride, 4,4′‐oxydiphthalic anhydride, 3,3′,4,4′‐benzophenone tetracarboxylic dianhydride and 4,4′‐(hexafluoroisopropylidene)diphthalic anhydride via a one‐pot high temperature polycondensation procedure to produce a series of aromatic polyimides. These polyimides exhibited excellent solubility even in common organic solvents, such as chloroform and tetrahydrofuran. The flexible and tough films can be conveniently obtained by solution casting. The films were nearly colorless and exhibited high optical transparency, with the UV cutoff wavelength in the range 302–365 nm and the wavelength of 80% transparency in the range 385–461 nm. Moreover, they showed low dielectric constants (2.73–3.23 at 1 MHz) and low moisture absorption (0.13%–0.46%). Furthermore, they also possessed good thermal and thermo‐oxidative stability with 10% weight loss temperatures (T_10%) in the range 489–507 °C in a nitrogen atmosphere. The glass transition temperatures of all polyimides are in the range 262–308 °C. Copyright © 2012 Society of Chemical Industry     

Effects of lithium perchlorate on poly(ethylene oxide) spherulite morphology and spherulite growth kinetics

Effects of lithium perchlorate (LiClO₄) on the crystallization behaviors of poly(ethylene oxide) (PEO) were investigated by differential scanning calorimetry (DSC), Fourier transform infrared spectroscopy (FTIR), and polarized optical microscopy (POM) in PEO/LiClO₄ system. DSC results indicate that there are nucleation effects of LiClO₄ on the crystallization of PEO. But, on the other hand, the coordination of lithium ion with the oxygen ether atoms of PEO can obviously reduce the crystallinity and spherulite growth rate of PEO. This contrary effect of LiClO₄ on the crystallization of PEO in PEO/LiClO₄ complexes system was analyzed and discussed in detail. The Laurizen–Hoffman theory was used to describe the Li‐coordinated crystallization kinetics of PEO spherulite. It showed that the nucleation constant (K_g) and folding surface free energy (σ_e) decreased with increasing LiClO₄ contents, and the energy necessary for the transport of segments across the liquid–solid interface (ΔE) increased on increasing the contents of LiClO₄. © 2011 Wiley Periodicals, Inc. J Appl Polym Sci, 2012