Simulation studies on a rotating ring disk electrode: Effects of ionic migration with kinetic complication-disk results

In continuation to my previous work (Guha S. AIChE J. 2013;59(4):1390-1399), in this work, effects of ionic migration are evaluated for disk region of a rotating ring disk electrode system by numerically solving complex differential equations, developed for mass transfer along with kinetic complication in presence of ionic migration under limiting current condition. The system for simulation is 0.01 M Fe₂(SO₄)₃ solution with H₂SO₄ as supporting electrolyte. Simulation cases are presence and absence of ionic migration with kinetic complication (oxidation of Fe²⁺ to Fe³⁺ under O₂ pressure). Results show that concentration boundary layer thickness of reactant Fe³⁺ reduces appreciably and steady-state disk current reduces substantially in presence of migration. Simulated steady-state disk current in absence of migration case agrees well with published data. Results indicate higher Fe²⁺ concentration in presence of migration and thereby higher rate of oxidation of Fe²⁺ to Fe³⁺ at all rate constant values.     

《物理化学》课程思政建设的探索与实践

"立德树人"是高等教育的根本任务,思政教育能培养青年大学生树立正确的价值观。以近三年的《物理化学》课程教学实践为基础,举例说明《物理化学》课程的思政元素提炼,讨论了如何在授课教学环节有机融入课程思政内容。结果表明,思政元素的融入不仅能有效提高教学质量,更能激发学生的爱国热情,培养学生的辩证思维,有利于培养有理想、有素养的高素质人才。     

Improvement in the properties of low carbon MgO-C refractories through the addition of graphite-SiC micro-composite

Graphite–SiC micro-composites have been prepared in–house by carbothermal reduction process. Controlling the process parameters including the weight ratio of SiO₂ to graphite as well as carbothermal reduction temperature during the micro-composite preparation favors the homogeneous formation of SiC with preferred morphologies like ribbons and whiskers/fibers. The micro-composite modified low carbon MgO-C refractories have exhibited significantly improved bulk properties over the standard composition. To understand the beneficial role of SiC reinforcement on hot strength performance under air oxidizing conditions, we propose a scaling parameter known as strength factor (fs) based on the ratio of hot strength (HMOR) to cold strength (CCS). Correlating the strength factor data (fs) with oxidative damage provides new insights into the reinforcing effects of distinct SiC morphologies in this new class of micro-composite fortified refractory systems over the standard compositions.     

Effect of sintering temperature on the transport properties of La2Ce2O7 ceramic materials

La₂Ce₂O₇ (LCO) based materials are of a paramount importance since they can be utilized for ammonium production, thermal barrier application, catalysts, hydrogen production and solid oxide fuel cells (SOFCs). In this work, a nano crystalline LCO powder was prepared using glycine-nitrate combustion method and then its properties were comprehensively characterized. The structural analysis of the synthesized LCO was carried out using conventional X-ray diffraction (XRD) and Raman spectroscopy. In a disordered phase, LCO is a biphasic mixture composed of C- and F-type phases. Densification studies were performed by sintering LCO pellets at different sintering temperatures. A densification of ≥95% was observed in all the samples with a very little variation. Sintering temperature had a marked effect on the electrical conductivity of LCO. The LCO sintered at 1100 °C showed the highest conductivity (3.68 mS/cm at 700 °C in air). The electrical conductivity was found to be decreasing with an increase in sintering temperature from 1100 to 1400 °C. To understand the behavior, the analysis of distribution function of relaxation times (DFRTs) utilized for correct separation of grain and grain boundary resistances. The presence of C- and F- type phases calculated from Raman spectra plays a crucial role in deciding conduction behavior of LCO. The results suggest a strong relationship between history of the ceramics preparation and their electrical properties.     

Notwendigkeit und Vermarktung von Flexibilitätsoptionen im Energiesystem der Zukunft

Demands on production, distribution and consumption of electrical energy change fundamentally with the energy revolution. Energy purchasing costs for inflexible consumers are rising and proceeds of inflexible producers are sinking. Companies are able to reduce costs by marketing operational flexibility options. This article sets out the need of flexibility in the energy system and the new marketing options. Flexibility potentials within infrastructure plants of a chemical park are analyzed, evaluated regarding marketing and activated in the presented research project FlexChemistry.     

Chemical Bonding by the Chemical Orthogonal Space of Reactivity

The fashionable Parr–Pearson (PP) atoms-in-molecule/bonding (AIM/AIB) approach for determining the exchanged charge necessary for acquiring an equalized electronegativity within a chemical bond is refined and generalized here by introducing the concepts of chemical power within the chemical orthogonal space (COS) in terms of electronegativity and chemical hardness. Electronegativity and chemical hardness are conceptually orthogonal, since there are opposite tendencies in bonding, i.e., reactivity vs. stability or the HOMO-LUMO middy level vs. the HOMO-LUMO interval (gap). Thus, atoms-in-molecule/bond electronegativity and chemical hardness are provided for in orthogonal space (COS), along with a generalized analytical expression of the exchanged electrons in bonding. Moreover, the present formalism surpasses the earlier Parr–Pearson limitation to the context of hetero-bonding molecules so as to also include the important case of covalent homo-bonding. The connections of the present COS analysis with PP formalism is analytically revealed, while a numerical illustration regarding the patterning and fragmentation of chemical benchmarking bondings is also presented and fundamental open questions are critically discussed.     

渣油催化临氢热转化钼铁双金属催化剂的研究

Replacement of precious single metal catalysts with cost-effective, highly-dispersed composite catalysts for catalytic hydrothermal conversion of residue holds tremendous promise for the residue upgrading technologies. Organic metals were added to the feed as the oil-soluble precursors, and transformed into the catalytic active phases in this work. Physical properties and structures of the composite catalysts had been investigated by X-ray fluorescence spectroscopy, X-ray photoelectron spectroscopy, X-ray diffraction, scanning electron microscope and transmission electron microscopy. The composite catalysts were found to be highly efficient in the catalytic hydrothermal conversion of both model compound and residue. Increased metal dispersion and synergistic effects of two metals played indispensable roles in such catalytic system. Results showed that under the test conditions in the article, the catalyst had the best catalytic performance when the mass ratio of molybdenum to iron was 1.5.     

基于QoE感知的星地一体化网络公平资源分配策略

星地一体化网络是卫星网络和地面网络互联，实现卫星网络和地面网络优势互补的一体化网络。随着无线通信的快速发展，卫星网络和地面网络的同频复用技术可有效提升资源利用效率，满足日益增长的无线数据业务需求。但由于无线数据业务类型的多样化和频谱资源的稀缺性，如何实现用户数据服务的服务体验质量（Quality of experience， QoE）和公平性提升也成为星地一体化网络亟待解决的关键问题。本文综合考虑信道时变性、服务体验多样性和服务公平性，提出了一种基于QoE感知的星地一体化网络资源分配策略。为此，将目标问题描述为基于时间平均的服务体验质量的网络公平效用最大化，并利用李雅普诺夫优化理论，将复杂的动态原始优化问题进一步转化并分解为3个瞬时优化子问题，每个子问题可以在每个时隙独立求解。同时，由于无线资源分配为典型的非凹混合组合优化问题，推导了一个低复杂度的两步算法来求解第三个资源分配子问题。仿真结果揭示了在不同的公平性参数下用户的长时QoE与公平性之间的折衷情况。     

基于深度EPG的智能导航平台建设

随着三网融合的大力推进以及双向互动业务的大力开展,运营商使用原有简单的EPG不足以支撑开展更多的增值业务,不能主动为用户推荐节目,不能为运营商带来新的收入机会。作为重要的创新能力支撑系统,介绍了江苏有线智能导航平台的设计与应用,为相关广电运营商提供一定的设计参考。     

Controlled synthesis of Ag2O/g-C3N4 heterostructures using soft and hard templates for efficient and enhanced visible-light degradation of ciprofloxacin

Pluronic 31R1 surfactant and MCM-41 silica were used to fabricate mesoporous Ag₂O/g-C₃N₄ heterostructures with improved surface areas. The fabricated mesoporous nanocomposite was used to photo oxidize ciprofloxacin. The TEM images of Ag₂O/g-C₃N₄ indicated a uniform dispersion of spherical approximately 4-nm Ag₂O nanoparticles on g-C₃N₄. The mesoporous 0.9% Ag₂O@g-C₃N₄ heterostructure exhibited 100% efficiency in ciprofloxacin oxidation within 60 min when compared with the 25% efficiency in 120 min of pure mesoporous Ag₂O and 10% efficiency in 120 min of pure g-C₃N₄. The highest ciprofloxacin oxidation efficiency achieved was 100%, which was four and ten times better than those of Ag₂O and g-C₃N₄, respectively. This superior performance of the mesoporous Ag₂O/g-C₃N₄ was attributed to the high dispersion of nano-sized mesoporous Ag₂O particles on the g-C₃N₄ surface, narrow bandgap, and significantly high surface areas. The powerful interaction between Ag₂O and g-C₃N₄ ensured robust durability of Ag₂O/g-C₃N₄ heterostructures, which is evident in the fact that five recycling trials of the photocatalyst rendered a minimal loss of efficiency.