离子液体［bmim］HSO4中合成的苯胺与环氧丙烷共聚物的电催化性能

 采用恒电流电解法,在1-丁基-3-甲基咪唑硫酸氢盐(［bmim］HSO4)离子液体中合成了苯胺与环氧丙烷共聚物(PAN-PPO). 扫描电镜观察表明, PAN-PPO由直径小于80 nm的纳米纤维组成. PAN-PPO对草酸氧化具有较好的电催化活性. 采用电化学原位红外光谱技术对草酸的电催化氧化进行了简单的分析.     

一种提高铂电催化氧化甲酸性能的简单方法

在离子液体1-乙基咪唑三氟乙酸盐(HElmTfa)中,采用循环伏安法在铂电极表面修饰聚吡咯(PPY),制得PPy-HEImTfa/Pt,并研究了其对甲酸的电催化氧化性能.与相同条件下的铂基底电极相比,PPy-HEImTfa/Pt对甲酸的电催化氧化性能有很大的提高.原位红外光谱表明,PPy-HElmTfa能降低中间体CO等对铂电极的毒化作用,促进甲酸直接氧化生成CO_2.     

混凝土断裂过程的力学模型与数值模拟

混凝土是一种典型的非均匀准脆性材料,其断裂过程是非常复杂的.评述了混凝土断裂以及断裂过程研究的进展状况,主要总结了一些研究混凝土断裂的宏观力学方法和模型,介绍了从混凝土的细观层次出发模拟其断裂过程的数值模型.最后,简单介绍了作者用细观数值方法模拟混凝土宏观断裂过程的研究成果.      

NUMERICAL STUDY ON PROPERTIES OF WEAK INTERLAYER OF LAMINATED COMPOSITE

<正>With assumption of material inhomogeneity on meso level,a three-point bending beam model has been adopted to simulate crack propagation in two dimensional laminated composite and to verify the toughening mechanism of energy dissipation and crack deflection along the weak interlayer.Moreover,the effect of strength,elastic modulus and thickness of the weak interlayer on both strength and toughness of the laminated composite have also been investigated in this paper.     

岩石声发射Kaiser效应的数值模拟试验研究

运用岩石破裂过程分析RFPA^2D系统,对岩石破裂过程中声发射Kaiser效应进行了数值模拟试验研究,得到了与物理试验现象十分吻合的模拟结果。     

基于数字图像处理的岩石细观破裂力学分析

将数字图像处理技术引入到岩石破裂过程分析RFPA2D(Rock Failure Process Analysis)系统,建立了岩石细观结构破坏过程分析方法．首先提取岩石的细观结构图像,再转化成RFPA2D的前处理数据和数值分析网格,然后进行应力求解和破坏分析．以花岗岩细观结构为例,阐述了运用基于数字图像处理技术的RFPA2D方法进行岩石细观结构破坏分析的过程．结果表明,在岩石破裂过程数值模拟分析中引入数字图像处理技术是岩石细观结构破坏力学行为研究的一种方便而有效的方法．     

超细碳化钨及其复合粉末的制备

超细碳化钨(WC)是近年发展起来的硬质合金材料，本文根据超细碳化钨粉末在还原碳化过程中是否连续，将其制备方法分成一步法和两步法进行综述。同时，归纳了超细WC-Co复合粉末的主要制备方法，其中喷雾干燥-流化床法具有操作过程连续、复合粉与反应气体接触充分、复合粉末的活性高、反应温度低和最终粉末的晶粒细小均匀等优点，可望作为制备超细碳化钨及其复合粉末的重要方法。     

Investigation of Platinum Dispersed on Reduced Graphene Oxide‐supported Tungsten Carbide via Sacrificial Cu Adlayers for Methanol Oxidation

Reduced graphene oxide‐supported tungsten carbide composite (WC/RGO) was prepared by program‐controlled reduction‐carburization technique. Scanning electron microscope (SEM) and transmission electron microscope (TEM) show that WC nanoparticles with a narrow distribution (10–20 nm) are highly dispersed both on the edge and between the layers of RGO. And then it was used as a support to load different low contents (no more than 0.4 wt%) of Pt via sacrificial Cu adlayers. The morphology and the electrocatalytic activity of the prepared catalysts were characterized by TEM and cyclic voltammograms (CV), respectively. The results indicate that a small amount of isolated Pt atoms show low or even no activity for methanol oxidation. With the increasing deposition cycles, the content of Pt and the ensembles of neighboring Pt atoms are increased, which makes the onset potential shift negatively and mass current density increase. The results demonstrate that controllable amount of Pt can be deposited on WC/RGO by galvanic displacement with Cu, and the extent and domain of Pt loading affect the electrochemical performance. Meanwhile, this research also provides another route to prepare a catalyst with ultra low noble metal on WC/RGO for solving the problem of high cost of the catalyst.     

Pd-Mn/Stainless Steel Wire Mesh Catalyst for Catalytic Oxidation of Toluene,Acetone and Ethyl Acetate

A new 0.1%Pd‐6%Mn/stainless steel wire mesh catalyst was prepared and used for volatile organic compounds (VOC) elimination. The supported palladium and manganese catalyst over the stainless steel wire mesh was prepared by using an impregnation method. When an anodic oxidation technology was employed, an anodic oxidation membrane appeared on the stainless steel wire mesh. On the 0.1%Pd‐6%Mn/stainless steel wire mesh catalyst calcined at 500°C, the total oxidation of toluene, acetone and ethyl acetate was respectively at 260, 220 and 320°C. The activity could be stable for over 700 h for toluene oxidation. The scanning electron microscopy (SEM) investigation of the Pd‐Mn/stainless steel wire mesh catalyst shows that the presence of anodic oxidation membrane on the support surface is important for better dispersion of active phases.     

活性炭表面性质对氧气扩散电极电催化性能的影响

 分别采用硝酸和空气氧化处理制得具有不同表面性质的粉末活性炭,并以此为催化层材料制成炭基氧气扩散电极,测定了不同电极的极化曲线和电化学阻抗谱. N2物理吸附和He程序升温脱附(He-TPD)研究表明,硝酸处理对活性炭孔结构的影响较小,但可使其表面含氧基团明显增加; 而空气氧化处理则会导致活性炭的中孔面积和孔容显著增大,但对表面含氧基团的影响较小. 极化曲线和电化学阻抗谱研究发现,当活性炭的孔结构相近时,电极的催化性能随着表面含氧基团的增多而急剧下降; 当活性炭表面含氧基团的量相近时,中孔孔容增大将导致电极催化性能的恶化. 与活性炭表面含氧基团相比,孔结构对氧气扩散电极的电化学性能具有更显著的影响.