用粉体表面改性技术制备拒水粉

拒水粉是一种新型建筑防水材料，被称之为神奇的粉末。本文就如何利用粉体表面改性技术制备拒水粉，从理论上和具体的实验方法上作了详尽的说明。     

Silicon doped carbon/Cu joints based on amorphous alloy brazing for first wall application

Amorphous ribbon-type filler-metals represent a promising selection for joining heterogeneous materials together. In this work, rapidly solidified ribbon-type Ti based amorphous filler with a melting temperature of 850 °C and a thickness up to 20 μm is used to join silicon doped carbon to pure copper. SEM examinations demonstrate that a high quality brazed joints could be acquired. The brazed seam has a uniform structure and pore free along its entire length. TiC and ZrC are formed near the interface of carbon and filler-metal when the brazing holds enough time. Using very thin Mo and Cu foil (0.2 mm in thickness) as multiple interlayer are very effective to mitigate the thermal stress occurred in the interface between carbon and copper. The shear strength of this carbon-multiple interlayer-copper joint is more than 20 MPa, and the rupture is mainly occurred on the carbon side.     

Preparation of ultra fine nickel-copper bimetallic powder for BME-MLCC

The preparation of ultra fine nickel-copper bimetallic powder with two-stage chemical reduction method was investigated. Reductive sugar and hydrazine hydrate were employed as reducing agent in different reductive stage, respectively. Reaction of CuSO₄·5H₂O with reductive sugar at 70 °C gives cuprous oxide and copper particles, then as-prepared mixture and nickelous hydroxide were reduced by hydrazine hydrate, and nickel-copper powder having excellent dispersibility was prepared. Influences of nickel added on composition and dispersibility of powder were studied. TG/DTG/DTA of nickel-copper powder, which is stable in room temperature, were discussed with thermal analyzer. Relation of nickel content to oxidation temperature was investigated. Ni-Cu bimetallic powder particles have a fully coated structure when nickel content is up to 30%. As-prepared nickel-copper powder was applied in base metal electrode-multilayer ceramic capacitor (BME-MLCC). The end termination has high adhesion force, fairly good densification, low resistivity, excellent solderibility behavior and resistance behavior to soldering.     

溶胶-凝胶法制备(Sr,Pb)TiO3纳米晶粉及表征

采用溶胶－凝胶法成功地合成了（Sr,Pb)TiO3纳米晶粉，并利用FTIR技术对凝胶的形成过程及350℃，1．5h煅烧获得的粉体材料进行了表征。实验以TG－DSC分析作为拟定煅烧温度的依据，以XRD作为煅烧产物的分析手段，最佳煅烧温度为600℃，所合成的（Sr,Pb)TiO3纳米晶粉的平均晶粒尺寸约为21nm，属钙钛矿型立方顺电相结构。     

Synthesis and microwave characterization of Co-SiC core-shell powders by electroless plating

Co-SiC core-shell powders were prepared by electroless plating. Scanning electron microscopy （SEM） revealed that Co-SiC core-shell powders were of nearly sphere-like shape and were about 0.3 pan. X-ray powder diffraction （XRD） patterns showed that the cobalt powder was hexagonal crystallite. The complex dielectric constant and the complex permeability of Co-SiC core-shell powders-paraffin wax composite were measured by the rectangle wavegnide method. It showed that the dielectric loss was less than 0.1 and the magnetic loss was about 0.2 in 8.2-12.4 GHz for prepared Co-SiC core-shell comoosite oowders.     

稀土钕对激光快速成形TC4合金组织及性能的影响

针对氢化脱氢钛合金粉末氧含量较高的问题，研究了添加稀土钕对激光快速成形TC4合金组织及性能的影响。结果发现，添加稀土Nd后，激光快速成形TC4合金的宏观晶粒尺寸变化不大；但随稀土添加量的增加，初始β列状晶逐渐转化为全β等轴晶，晶粒内部的魏氏α组织逐渐转变为网篮α，粗化α条不断增多，呈现团束聚集趋势，晶界α集束体积分数也不断增大；随稀土添加量的增加，激光快速成形TC4合金的室温塑性先大幅度提高，然后急剧降低；稀土添加量为0．1％～0．2％（质量分数，下同）时，氧含量为0．26％的氢化脱氢TC4合金粉末激光快速成形件沉积态的抗拉强度达975MPa，延伸率9．5％，满足锻件标准要求。     

Ti(C,N)粉末制备技术的研究及进展

概括了国内外Ti(C,N)粉末的制备技术,特别系统地介绍了Ti(C,N)粉末的制备技术的最新进展,分析了这些制备技术的工艺过程和工艺特点,讨论了其存在的问题和发展趋势。     

快速凝固铝硅合金粉末加热过程中硅颗粒的粗化行为

利用差示扫描量热仪(DSC)、电子显微镜等设备对Al-12.8%Si合金粉末的原始状态及热处理后的状态进行了分析。发现其显微组织有两个连续的变化过程:在156℃时,固溶在基体Al中的过饱和Si开始析出,并在340℃发生粗化,随着加热温度的升高,粗化现象仍然存在。另外,对Si颗粒的粗化机理进行了研究,发现其粗化符合经典的LSW理论。     

用相变方法制取高纯度超细钽粉的研究

报导了通过相变热处理使Ｋ２ＴａＦ７晶体参数发生变化，以利于制取高纯度超细钽粉的实验依据和结果。结果表明，Ｋ２ＴａＦ７在２００～２５０℃发生可逆相变；相变后Ｋ２ＴａＦ７晶体的粒径可由原来的１３５１．８μｍ减小至７０．８μｍ，极大地提高了比表面积；相变后，杂质极大挥发，提高了Ｋ２ＴａＦ７的纯度。     

各向异性Sm2Fe17Nx磁粉的结构与磁性能

研究了Sm2Fe12Nx磁粉的制备、结构与磁性能，发现Sm—Fe合金的铸态组织主要由Sm2Fe17、α—Fe和SmFe2三种物相组成，而经过1000℃均匀化退火48h处理后富Sm的SmFe2相基本消失，α—Fe相的品粒变小，数量减少。随着氯化时间延长到10h，Sm2Fe17相始终未改变其Th2Zn17型结构，而氯原子浓度增加，所有的X射线衍射峰均向小角度方向移动；但在氮化时间超过10h后，物相要发生变化，导致磁性能降低。在500℃下流动的氮气氛中对Sm2Fe17合金氮化2、4、6、10h未加磁场取向的磁粉中，以氮化6h的磁性能值最高：σr＝35．44Am^2/kg(emu／g)，Hc＝58kA／m(729．03Oe)。磁性能值偏低的原因与测量磁场较低，粒径分布不均匀及粒径较大有关。