三维碗状结构CoS2/C复合材料的制备及其在超级电容器中的应用

以二氧化硅为硬模板,采用碳化和硫化工艺制备出具有三维碗状结构的CoS_2/C复合材料.利用XRD,Raman和XPS研究了所制备材料的相组成,晶体结构,元素组成和价态.利用SEM和TEM对其微观形貌进行了表征,并采用电化学工作站分析了CoS_2/C作为超级电容器电极材料的电化学性能.结果表明:三维碗状结构CoS_2/C复合材料具有优良的电化学性能,在1 A/g的电流密度下比容量可以达到466 F/g.将CoS_2/C和N-rGO分别作为正极和负极组装的水系非对称超级电容器器件的电压窗口可以拓宽到1.6 V.该器件在0.5 A/g的电流密度下能量密度可以达到13.6 wh/kg,功率密度达到374.5 w/kg.在3 A/g的电流密度下经过5000次循环充放电后容量保持率达到了87%.     

Highly active sites of low spin FeⅡN4species:The identification and the ORR performance

Over recent years,catalytic materials of Fe-N-C species have been recognized being active for oxygen reduction reaction(ORR).However,the identification of active site remains challenging as it generally involves a pyrolysis process and mixed components being obtained.Herein Fe₃C/C and Fe₂N/C samples were synthesized by temperature programmed reduction of Fe precursors in 15%CH₄/H₂and pure NH₃,respectively.By acid leaching of Fe₂N/C sample,only single sites of FeN₄species were presented,providing an ideal model for identification of catalytic functions of the single sites of FeN₄in ORR.A correlation was conducted between the concentration of Fe^ⅡN₄in low spin state by Mossbauer spectra and the kinetic current density at 0.8 V in alkaline media,and such a structure-performance correlation assures the catalytic roles of low spin Fe^ⅡN₄ species as highly active sites for the ORR.     

基于统计软件R的安全壳泄漏率试验数据有效性分析

安全壳泄漏率计算过程中，最重要的环节是以不同时刻测量数据对时间进行线性回归分析。对回归的显著性检验以及方差分析是评价试验结果有效性的重要手段。本文基于统计软件R对某电厂调试阶段安全壳泄漏率试验的数据进行分析，通过对线性回归模型的独立性、正态性和异方差性检验以及极端样本点的剔除等方式，探讨泄漏率计算前的回归诊断对计算结果可靠性的影响。通过回归诊断的实例分析发现，在安全壳泄漏率计算的数据样本中，可能存在自相关、非正态和异方差性等问题影响回归结果，进而影响泄漏率的最终结果。因此，在计算泄漏率结果时，须通过回归诊断方法评价数据的有效性，对不能通过检验的样本应通过适当方法对最终结果进行修正。      

The formation of fibrous structure of polyamide 6 induced by the three-step forming process and its prominent reinforcement in nitrile rubber

Nitrile rubber (NBR) blends with excellent performance have always been a hot research topic in petroleum field. Due to the excellent performance and compatibility of polyamide 6 (PA6), it provides an opportunity for the preparation of high-performance NBR/PA6 blends. In this article, NBR/PA6 blends were prepared by the three-step molding process. Experimentally, it was found that PA6 has a prominent reinforcement effect in NBR matrix. The variation of this mechanical property was investigated from different aspects of the crystal structure, crystallinities, phase morphology, and so on. It can be cleared that the formation of fibrous structure of PA6 phase is the main factor for reinforcement of the polymer blends. Meanwhile, the formation mechanism of the special phase structure induced by the three-step process is deeply expounded and its structural evolution schematic is established. © 2019 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2019 , 136, 47472.     

盐酸氨溴索有关物质的合成

为控制盐酸氨溴索质量,以外购的有关物质E(2-氨基-3,5-二溴苯甲醛)为起始原料,合成了4个有关物质:2-氨基-3,5-二溴苯甲醇(有关物质A)、反式-4-(6,8-二溴-1,4-二氢喹唑啉-3(2H)-基)环己醇(有关物质B)、反式-4-[[(E)-2-氨基-3,5-二溴苯亚甲基]氨基]环己醇(有关物质C)和顺式-4-[(2-氨基-3,5-二溴苯甲基)氨基]环己醇(有关物质D),通过~1HNMR、~(13)CNMR和MS对产物结构进行了确证,并优化了醛胺缩合和还原反应条件。合成的这4个有关物质可作为盐酸氨溴索质量控制的杂质对照品。     

稀土石膏常压酸化法制备硫酸钙晶须的研究

以含稀土的石膏为原料运用常压酸化法合成硫酸钙晶须,探讨了不同工艺条件对生成的硫酸钙晶须形貌的影响,同时还考察了晶型助长剂的种类和晶型助长剂的含量对硫酸钙晶须生长的影响,利用SEM和XRD分别对硫酸钙晶须的表面形貌、物相特征做了表征分析。实验得到制备硫酸钙晶须的最佳的反应条件：稀土石膏质量浓度为0.22 g/mL、反应时间为25 min、盐酸浓度为2.8 mol/L、反应温度为70 ℃、陈化时间为4 h,在此条件下合成的硫酸钙晶须平均长度为61 μm,平均长径比为30.5;通过对比实验选出了CuCl₂作为促进硫酸钙晶须生长的助长剂,在添加5%（质量分数）的CuCl₂的情况下可使硫酸钙晶须长径比从30.5增至41,长度从61 μm增至81 μm。     

Effects of B2O3 on Crystallization,Structure, and Heat Transfer of CaO-Al2O3-Based Mold Fluxes

Metallurgical and Materials Transactions B - The reaction between traditional CaO-SiO2-based mold fluxes and high-Al steel inevitably changes flux composition, and, consequently, flux properties....     

Evaluation of bismuth doped La2-xBixNiO4+δ (x = 0, 0.02 and 0.04) as cathode materials for solid oxide fuel cells

Bismuth doped La_2-xBi_xNiO_4+δ (x = 0, 0.02 and 0.04) oxides are investigated as SOFC cathodes. The effects of Bi doping on the phase structure, thermal expansion, electrical conduction behavior as well as electrochemical performance are studied. All the samples exist as a tetragonal Ruddlesden-Popper structure. Bi-doped LBNO-0.02 and LBNO-0.04 have good chemical and thermal compatibility with LSGM electrolyte. The average TEC over 20–900°С was 13.4 × 10^?6 and 14.2 × 10^?6 K^?1 for LBNO-0.02 and LBNO-0.04, respectively. The electrical conductivity was decreasing with the rise of Bi doping content. EIS measurement indicates Bi doping can decrease the ASR values. At 750 °C, the obtained ASR for LBNO-0.04 is 0.18 Ωcm², which is 56% lower than that of the sample without Bi doping, suggesting Bi doping is beneficial to the electrochemical catalytic activity of LBNO cathodes.