山东栖霞—大柳行地区金矿找矿靶区地质评价及优选

栖霞—大柳行地区位于胶东中部栖霞—蓬莱金矿成矿带内，是胶东重要的金成矿区，成矿条件优越。为了对圈定靶区进行优选分类，通过对该区地质背景、找矿靶区评价、找矿靶区优选方面展开综合研究，并结合勘查工作程度和矿业权设置情况，划分出3类预测区，选定了5个靶区为今后优先部署勘查工作的方向。     

安徽省铜陵市铁山头铜矿床地质特征及找矿潜力

铁山头铜矿床处于铜陵矿集区的中东部，属于扬子陆块下扬子凹陷中的铜陵隆起。矿床位于凤凰山矿田北侧，成矿潜力较大。综合研究分析认为：①接触交代作用使得岩体接触带及附近变质形成矽卡岩矿化带；②区内凤凰山岩体（花岗闪长岩）系成矿母岩；③矿体主要赋存于花岗闪长岩与三叠系下统南陵湖组石灰岩接触带上；④矿床成因类型为高—中温热液交代矽卡岩型矿床。     

广西箭猪坡矿床首次发现的石英脉型锡矿体特征及 锡石微量元素地球化学意义

箭猪坡矿床是丹池成矿带南端的一个以铅锌锑为主的矿床，随着2012-2014年在箭猪坡矿床钻孔中石英脉型锡矿体的首次发现，打开了箭猪坡矿床新的找矿空间。新发现的锡矿体矿石矿物组合类型主要为锡石+闪锌矿+脆硫锑铅矿+黄铁矿+石英及锡石+脆硫锑铅矿+石英+方解石。箭猪坡矿床锡石呈自形-半自形粒状，锡石粒径多在0.1～0.2mm，少数0.02～0.05mm，分布在含硫化物的石英脉裂隙中。物相分析显示箭猪坡矿床锡主要赋存在锡石中，锡石物相占83.33%～100%。阴极发光（CL）图像显示箭猪坡矿床中的锡石经历了两期结晶作用：早期锡石（Ⅰ）和晚期锡石(Ⅱ），早期锡石CL荧光亮度较小，呈暗灰色至黑色；晚期CL荧光亮度较大，呈白色至浅灰色。锡石单矿物SnO2含量91.623%～96.288%，平均94.03%，杂质主要有Fe、W、In等，其中FeO含量0.02%～0.52%，WO3含量多在0.02～1.34%，In2O3含量在0.476%～0.954%，Sn与FeO、In2O3呈负相关，锡石中FeO、WO3、Ta2O5、Nb2O5、MnO含量指示箭猪坡锡形成于中低-中温热液环境，成矿热液来源于高度分异演化的花岗质岩浆。通过与大厂矿田西矿带上部脉状锡矿体的类比分析，具有相似的成矿条件及矿物组合，推测所揭露到的脉状锡矿（化）体相当于西矿带上部脉状锡矿（化）体，而下部的网脉状、似层状锡矿体尚未揭露到，由此预测箭猪坡矿床深部找矿空间及找矿潜力大。     

Measurement of residual stresses in dissimilar friction stir-welded aluminium and copper plates using the contour method

The longitudinal residual stresses in the friction stir-welded plates of 5A06 aluminium and pure copper were determined using the contour method. The results revealed the presence of high tensile and compressive residual stresses on the aluminium and copper sides, respectively. The residual stresses were detected on the weld zone as well as the thermo-mechanically affected zone (TMAZ) of the aluminium plate. In contrast, the compressive residual stresses in the copper plate had a much narrower width along the weld line. Peak tensile stresses up to 240?MPa were found in the TMAZ of the aluminium plate.     

Cf/C复合材料与纯铜的胶接辅助钎焊连接

采用胶接辅助钎焊方法,以TiH_2粉为活性元素源,环氧树脂为粘性载体,Ag-Cu共晶合金为钎料,Cu箔为应力缓冲层材料,实现了C_f/C复合材料与纯铜的钎焊连接,结果表明,接头界面处产生TiC,TiCu,Ag(s,s),Cu(s,s)等反应产物,其结构可表示为(C_f/C)/TiC+Ag(s,s)+Cu(s,s)+TiCu/Cu。通过钎焊工艺试验得出,在930℃保温25 min钎焊条件下接头的抗剪强度达到最大值30 MPa。     

Thermal stability of CaCu3Ti4O12: Simultaneous thermal analysis and high-temperature mass spectrometric study

Thermal stability of calcium copper titanate was studied by differential scanning calorimetry, thermogravimetry and high-temperature mass spectrometry. Calcium copper titanate (CCTO) had no thermal effects and mass losses caused by thermal dissociation or any phase transitions, besides melting, in the temperature range of 298–1423?K. The melting point of calcium copper titanate is 1398?K. The endothermic effect at 1250?K was associated with the decomposition of copper (II) oxide segregated in the intergrain space of the CaCu₃Ti₄O₁₂-CuO ceramics. In this connection, we proposed a simple method for estimating the content of copper oxide in the CaCu₃Ti₄O₁₂-CuO composite. The processes of evaporation of CaCu₃Ti₄O₁₂ in the temperature range of 1500–2100?K were studied by high-temperature mass spectrometry. In the temperature range of 1500–1750?K, easily volatilized copper oxide was evaporated selectively from the calcium copper titanate. At the temperature of 2100?K, atomic calcium and titanium oxides, TiO and TiO₂, were present in the vapor.     

Surface structural and solar absorptance features of nitrate-based copper-cobalt oxides composite coatings: Experimental studies and molecular dynamic simulation

The copper and cobalt oxides composites coatings on aluminum substrates have been successfully synthesized via sol-gel method using nitrate-based sol precursors. The composites were characterized by X-ray Diffraction (XRD), X-ray photoelectron spectroscopy (XPS), Field Emission Scanning Electron Microscopy (FESEM), Atomic Force Microscopy (AFM), and UV–Vis–NIR spectrophotometry. The sol-gel reactions were discussed and Molecular Dynamics (MD) simulation was integrated into the study to predict molecules assembly properties. The XRD analyses revealed that the CuO and the Co₃O₄ composites were formed after the annealing process with the average difference of the calculated lattice parameters compared to ICDDs was 1.17%. The surface electronic structure was mainly consisted of tetrahedral Cu(I), octahedral Cu(II), tetrahedral Co(II), octahedral Co(III) as well as surface, sub-surface and lattice oxygen O^?. The XRD, XPS and MD simulation results showed that there was minimal (or possibly non-existing) indication of copper-cobalt mixed phase oxides formations. FESEM and AFM surveys revealed that the coating had a porous surface composed of interlinked nanoparticles in the range of ~?10 to ~?40?nm. UV–Vis–NIR reflectance spectra showed that the sol precursors concentration and the dip-drying cycle significantly influenced the absorptance value with optimum absorptance (α) of 88.7% exhibited by coating synthesized using sol concentration of 0.1?M and 10 dip-drying cycles. High absorptance value and simplicity in the synthesis process render the coatings to be very promising candidates for solar selective absorber (SSA) applications.     

Numerical study of flow distribution uniformity for the optimization of gradient porosity configuration of porous copper fiber sintered felt for hydrogen production through methanol steam reforming micro-reactor

A macroscopic numerical method is proposed to study the flow distribution uniformity of a novel porous copper fiber sintered felt (PCFSF), which has gradient porosities and was developed as the methanol steam reforming micro-reactor catalyst support for hydrogen production for fuel cell applications. The macroscopic porous media developed by the ANSYS/FLUENT software is used to represent the PCFSF. Our results indicate that the gradient porosity can reshape the flow distribution of PCFSFs greatly, thus producing significant influence on their performance. It is further revealed that, for a PCFSF with a determined gradient porosity configuration but different reactant feed directions, the velocity uniformity can be used as a quantitative criterion to evaluate the performance of hydrogen production. Furthermore, new gradient PCFSFs are produced according to the flow distribution of original gradient PCFSFs. The preliminary experimental results of the new gradient PCFSFs of 0.8-0.9-0.7 and 0.7-0.9-0.8 exhibit better methanol conversion and H₂ flow rate. This indicates that the numerical method can be used for the optimization of PCFSFs' gradient porosity configuration, which consists of the shape and position of the interfaces between different porosity portions, the number of interfaces and the porosity distribution in different portions.     

Carbon supported bimetallic Ru‐Co catalysts for H2 production through NaBH4 and NH3BH3 hydrolysis

This work investigates the effect of the addition of small amounts of Ru (0.5‐1 wt%) to carbon supported Co (10 wt%) catalysts towards both NaBH₄ and NH₃BH₃ hydrolysis for H₂ production. In the sodium borohydride hydrolysis, the activity of Ru‐Co/carbon catalysts was sensibly higher than the sum of the activities of corresponding monometallic samples, whereas for the ammonia borane hydrolysis, the positive effect of Ru‐Co systems with regard to catalytic activity was less evident. The performances of Ru‐Co bimetallic catalysts correlated with the occurrence of an interaction between Ru and Co species resulting in the formation of smaller ruthenium and cobalt oxide particles with a more homogeneous dispersion on the carbon support. It was proposed that Ru^°, formed during the reduction step of the Ru‐Co catalysts, favors the H₂ activation, thus enhancing the reduction degree of the cobalt precursor and the number of Co nucleation centers. A subsequent reduction of cobalt and ruthenium species also occurs in the hydride reaction medium, and therefore the state of the catalyst before the catalytic experiment determines the state of the active phase formed in situ. The different relative reactivity of the Ru and Co active species towards the two investigated reactions accounted for the different behavior towards NaBH₄ and NH₃BH₃ hydrolysis.