MoS2-mesoporous LaFeO3 hybrid photocatalyst: Highly efficient visible-light driven photocatalyst

Perovskite type materials have high potential photocatalytic application towards both hydrogen energy generation and organic dye degradation due to their high stability and good reusability. Here, it is the first analysis of photocatalytic degradation of RhB and hydrogen energy evolution under visible light over MoS₂/LaFeO₃ nanocomposite. The physicochemical properties of the materials were characterized using a range of techniques such as XRD, TEM, XPS, FTIR, PL, photocurrent, etc. The optical properties of the nanocomposite show good absorption in UV-Vis spectra as compared to the bare LaFeO₃. In this study, MoS₂/LaFeO₃ nanocomposite was synthesized through single step in situ hydrothermal processes with a narrow bandgap, enhanced photocatalytic application under visible light. This novel MoS₂/LaFeO₃ nanocomposite is an efficient and promising photocatalyst for both hydrogen energy evolution and organic dye degradation.     

Magnetic field coupling microfluidic synthesis of Fe2Pt/C nanocatalysts for enhanced electrochemical catalytic oxidation of alcohol

The influence of magnetic field (MF) on electrochemical catalytic properties of carbon supported Fe₂Pt nanocatalysts is investigated. Nanocatalysts are produced through an external MF coupled microfluidic process. X-ray diffraction (XRD) measurements show that Fe₂Pt nanocrystals (NCs) with larger sizes are synthesized when an external MF of 1.4 T is applied. X-ray photoelectron spectroscopy (XPS) and transmission electron microscopy (TEM) characterizations confirm that more Pt²⁺ reduces to Pt⁰ and NCs grow larger under magnetic fields (MFs) than those without MFs. The increased coercivity indicates that more surface unpaired electrons are present and the surface spin configuration changes under MFs. NCs synthesized under MFs show better catalytic performance in alcohol electrochemical catalytic oxidation reactions compared to samples synthesized without MFs. The mass activities significantly increase by 1.10 and 1.24 times and the specific activity increases up to 1.11 and 1.26 times for methanol and ethanol oxidation, respectively, compared to those without MFs.     

简析变压器油的生产工艺及质量

本文简要介绍了变压器油的运用价值,同时分析如何实现对变压器油生产工艺的优化,并从物理性能以及化学性能两个方面分析生产工艺改良后变压器油整体质量,以期为变压器油生产工作提供一定的参考与帮助。     

浅谈国际工程项目的技术标编制流程

本文将重点从阅读业主招标文件开始,以及参与业主组织的现场勘查和投标会议,成立投标组、会标、审标直至最后标书递交等各个阶段,并结合近几年参与国际工程项目投标的经验和体会去分析和探讨。     

SFEP文本因果关系提取及其与SFN转化研究

为将系统故障演化过程(system fault evolution process，SFEP)的文本描述转化为空间故障网络(space fault network，SFN)结构，用于故障分析，本文提出SFEP文本因果关系提取方法，及其与SFN基本结构的转化方法。首先给出SFEP中事件的几种典型因果关系。随后提出因果关系与SFN基本结构的转化流程。本文方法围绕着关键字和因果关系组模式展开，通过模型的不断学习补充和丰富关键字和组模式。最终使方法具备将SFEP文本转化为SFN结构的能力。以飞机起落架故障发生过程文本为例进行了应用，实验结果表明该方法可用于SFEP文本中的因果关系分析，并得到了理想的SFN。完善的关键字和组模式有利于使用计算机智能处理SFEP的SFN。     

引入气相对D类颗粒间歇卸料过程特性的影响

通过测量并分析引入气相前后D类颗粒间歇卸料过程中示踪颗粒的流动状态、压力分布和颗粒流率，发现床体内气固两相流动特性不仅随时间变化，还受到气速（正负压差）的影响。据此将卸料过程按时间分为3个阶段：初始蓄压（PS）阶段、稳定卸料（SD）阶段和非满管流（PP）阶段；并给出各卸料阶段不同正、负压差和重力条件下的气固流动特性。在时间较长、流场较为稳定的SD阶段，发现卸料口颗粒阻力是影响颗粒流率的关键参数，通过修正De Jong公式、Beverloo公式，依次建立卸料口颗粒阻力、D类颗粒卸料流率预测模型，与实验值吻合较好，有望为引入气相调控D类颗粒卸料流率的方法提供参考。     

煤与不同原料重整气化制甲醇对CO2排放的影响

通过介绍煤制甲醇对整个煤化工行业CO2排放的影响,选择以煤制甲醇工艺CO2排放为研究对象,分别叙述了煤气化制合成气,煤与天然气、煤与焦炉气以及煤与重质油重整气化制合成气联合生产甲醇过程中,吨甲醇产品工艺CO2排放情况,探讨不同煤气化形式对工艺CO2排放的影响因素,为如何通过气化工艺选型,降低煤制甲醇生产过程中工艺CO2排放量提供理论判断依据。     

海藻化工以氢氧化钙作为钙化剂的新型钙化工艺研究

研究了海藻化工中以氢氧化钙作为钙化剂的新型钙化工艺,使用氢氧化钙+氯化钙作为褐藻酸钠的钙化剂替代传统的单一氯化钙。确定的双钙钙化工艺条件：每升褐藻酸钠胶液（褐藻酸钠质量浓度为2.5 g/L）,添加氯化钙溶液29.0 mL（质量分数为5%）,添加氢氧化钙溶液13.75 mL（质量分数为5%）,复合钙化剂中氯化钙与氢氧化钙物质的量比为1.19∶1。与传统工艺相比,新型钙化工艺褐藻酸钠的产率未有明显变化,得到的褐藻酸钠粘度稍有降低,粘度由275.1 mPa·s降低至241.3 mPa·s;氯化钙使用量降低40%以上,总钙添加量减少19%。双钙钙化工艺实现了对钙化废水的再利用,废水中钙质量浓度经处理由483 mg/L降到20 mg/L左右,电导率由6.84 mS/cm降至4.28 mS/cm;经脱钙处理的钙化废水回用后对产品褐藻酸钠的产率和粘度没有显著影响。新工艺操作简单,不仅有效减少了钙化废水中离子的引入,同时可以实现低成本地脱钙,脱钙后的废水可以作为冲稀水回收利用,减少了水资源的消耗,为海藻化工行业的减排提供了一条新的工艺途径。     

Thermodynamic and economic analyses of a coal and biomass indirect coupling power generation system

The coal and biomass coupling power generation technology is considered as a promising technology for energy conservation and emission reduction. In this paper, a novel coal and biomass indirect coupling system is proposed based on the technology of biomass gasification and co-combustion of coal and gasification gas. For the sake of comparison, a coal and biomass direct coupling system is also introduced based on the technology of co-combustion of coal and biomass. The process of the direct and the indirect coupling system is simulated. The thermodynamic and economic performances of two systems are analyzed and compared. The simulation indicates that the thermodynamic performance of the indirect coupling system is slightly worse, but the economic performance is better than that of the direct coupling system. When the blending ratio of biomass is 20%, the energy and exergy efficiencies of the indirect coupling system are 42.70% and 41.14%, the internal rate of return (IRR) and discounted payback period (DPP) of the system are 25.68% and 8.56 years. The price fluctuation of fuels and products has a great influence on the economic performance of the indirect coupling system. The environmental impact analysis indicates that the indirect coupling system can inhibit the propagation of NO_x and reduce the environmental cost.     

中锰Q&P钢连续退火过程碳元素分配行为

采用扫描电镜、X射线衍射等研究了连续退火工艺中退火、淬火和配分等关键过程参数对中锰Q&P钢碳元素分配行为的影响,并分析了相应工艺条件下残留奥氏体量与碳含量的关系。结果表明:两相区退火温度的提高会导致奥氏体中的碳含量下降,微观组织表现为奥氏体含量增加,渗碳体量减少;退火时间10~60 s时,随着退火时间的延长,奥氏体含量和碳含量急剧增加,60 s后基本保持稳定;试验条件下淬火温度对残留奥氏体及碳含量的影响不显著;配分温度350~500℃时,随着配分温度的提高,奥氏体含量和碳含量呈现先增加后减小的趋势,配分温度450℃时均达到最大值;延长配分时间,残留奥氏体含量呈现先减少后增大再减少的趋势,残留奥氏体中的碳含量先减小后增加。