球磨对超重力下自蔓延离心熔铸Ti-B-W-C系复相陶瓷微观形貌及力学性能的影响

采用行星式球磨机对超重力离心熔铸Ti-B-W-C复相陶瓷的原始粉料进行球磨,通过对球磨转速的控制得到不同研磨程度的粉料,通过对制得的复相陶瓷进行微观结构和力学性能分析,发现随着球磨机转速的提高,球磨效率大大改善,粉料大幅度细化,Al粉以团絮状均匀附着在片状Ti和WO3晶粒周围.对粉料进行烧制,成功得到宏观致密、微观夹杂和气孔等缺陷明显减少、硬度等力学性能明显提升的复相陶瓷.     

Heterogeneous sono-Fenton-like process using martite nanocatalyst prepared by high energy planetary ball milling for treatment of a textile dye

High energy planetary ball milling was applied to prepare sono-Fenton nanocatalyst from natural martite (NM). The NM samples were milled for 2–6 h at the speed of 320 rpm for production of various ball milled martite (BMM) samples. The catalytic performance of the BMMs was greater than the NM for treatment of Acid Blue 92 (AB92) in heterogeneous sono-Fenton-like process. The NM and the BMM samples were characterized by XRD, FT-IR, SEM, EDX and BET analyses. The particle size distribution of the 6 h-milled martite (BMM₃) was in the range of 10–90 nm, which had the highest surface area compared to the other samples. Then, the impact of main operational parameters was investigated on the process. Complete removal of the dye was obtained at the desired conditions including initial pH 7, 2.5 g/L BMM₃ dosage, 10 mg/L AB92 concentration, and 150 W ultrasonic power after 30 min of treatment. The treatment process followed pseudo-first order kinetic. Environmentally-friendly modification of the NM, low leached iron amount and repeated application at milder pH were the significant benefits of the BMM₃. The GC–MS was successfully used to identify the generated intermediates. Eventually, an artificial neural network (ANN) was applied to predict the AB92 removal efficiency based upon the experimental data with a proper correlation coefficient (R² = 0.9836).     

Microstructural characterisation of nanoparticles using, XRD line profiles analysis, FE-SEM and FT-IR

In this investigation, the structural characteristics of α- Fe₂O₃ nanoparticles synthesised by a mechanical milling have been explored. The structure and morphology of samples were characterized by X-ray powder diffraction, field-emission scanning electron microscope (FE-SEM) and FT-IR measurements. The crystallite size and internal strain were evaluated by XRD patterns using Williamson-Hall and Scherrer methods. The results did not reveal any phase change during the milling. The average particle size decreases with a prolongation of milling times, while the lattice parameters and internal strain increase. It was found that using this method allowed the formation of hematite nanoparticles.     

球磨法对不同基质上转换发光的影响

分别利用高温固相法和高能球磨法,在反应温度为1 100℃、反应时间为2 h的条件下合成了以Y2O3、La2O3、LiTaO3为基质的双掺和三掺Tm3+、Er3+、Yb3+发光粉。XRD测试结果表明,高能球磨法制备的Y2O3、La2O3、LiTaO3材料的相纯度高于高温固相法。用980 nm红外激光分别对两种合成方法制得的样品粉末进行发光性质的检测,结果表明高能球磨法制得样品的发光强度高于高温固相法样品。不同基质样品的上转换发光性质表现为:Tm3+、Yb3+掺杂呈蓝光;Er3+、Yb3+掺杂呈黄光;Tm3+、Er3+、Yb3+三掺样品的发光减弱,颜色可调。     

球磨法对不同基质上转换发光的影响

分别利用高温固相法和高能球磨法,在反应温度为1 100 ℃、反应时间为2 h的条件下合成了以Y₂O₃、La₂O₃、LiTaO₃为基质的双掺和三掺Tm³⁺、Er³⁺、Yb³⁺发光粉。XRD测试结果表明,高能球磨法制备的Y₂O₃、La₂O₃、LiTaO₃材料的相纯度高于高温固相法。用980 nm红外激光分别对两种合成方法制得的样品粉末进行发光性质的检测,结果表明高能球磨法制得样品的发光强度高于高温固相法样品。不同基质样品的上转换发光性质表现为：Tm³⁺、Yb³⁺掺杂呈蓝光;Er³⁺、Yb³⁺掺杂呈黄光;Tm³⁺、Er³⁺、Yb³⁺三掺样品的发光减弱,颜色可调。     

固体颗粒的结构演化与机械力化学效应

干法、室温振动研磨制备铝超微颗粒, 分别将研磨2 h, 4 h和8 h的铝粉, 在常温下超声水解得到白色Al(OH)₃胶体, 水解产品经干燥、研磨、焙烧后制备出多孔、片状γ -Al₂O₃纳米颗粒, 粒度分布在30---50 nm之间. 借助于X射线衍射(XRD)分析方法和透射电子显微镜(TEM), 研究固体颗粒在细化过程中的能量转换, 分析颗粒的微结构演化与机械力化学反应的关系, 确定理想的研磨时间. 研究结果表明: 固体颗粒在机械力的作用下产生大量的应变和位错缺陷, 使材料处于亚稳、高能活性状态, 易于诱发机械力化学反应, 在一定条件下晶体的表面能、应变能和层错能相互转化; 研磨2 h的铝颗粒内部, 晶格畸变和位错概率最大, 材料显示出极高的化学反应活性, 在超声波激发下, 储存在材料内部的能量被充分释放, 在较短的时间内, 水解生成Al(OH)₃纳米颗粒.     

Ultra-fine grained Nd–Fe–B by high pressure reactive milling and desorption

This paper reports on the grain refinement in dynamic hydrogenation disproportionation desorption and recombination (d-HDDR) processed Nd-rich Nd₂Fe₁₄B and stoichiometric Nd₂Fe₁₄B powders using high pressure reactive milling (HPRM) followed by a subsequent desorption and recombination. In contrast to the dynamic-HDDR processed anisotropic powder with a grain size of the Nd₂Fe₁₄B phase of 300 nm, the new approach yields a further reduction of the Nd₂Fe₁₄B₁ grain size to less than 70 nm. Nd-rich Nd₂Fe₁₄B powder produced by HPRM and subsequent desorption exhibits a coercivity μ_0iH_c=1.35 T and a remanence of 0.80 T. In the stoichiometric material, the reduction of the Nd-content leads to an increase in remanence to 0.85 T. Additionally, it is demonstrated that highly anisotropic powders can also be obtained by dynamic-HDDR processing of stoichiometric Nd₂Fe₁₄B powders.     

Dry modification of electrode materials by roller vibration milling at room temperature

For the first time dry roller vibration milling at room temperature was used to prepare active carbon （AC） nano-particles and to modify MnO2 powder as electrode materials. In 30 min AC was milled to a mean particle size of 30-50 nm with increased crystallinity and higher specific surface area, predominantly mesoporous and with improved pore diameter distribution. Then, AC nano-particles were incorporated with MnO2 or bismuth-doped MnO2 nano-particles synthesized by sol-gel methods to prepare nano-composite electrode materials for studying their electrochemical performance. The AC nano-particles combined with 10 wt.% bismuth-doped MnO2 nano-particles were found to possess excellent electrochemical property with specific capacitance up to 308 F/g and without obvious attenuation with increasing current. Our method seems to ooen a new way to imorove AC based electrode materials used for clean energy such as suner capacitors.     

Raman microspectroscopic mapping or thermal system used to investigate milling‐induced solid‐state conversion of famotidine polymorphs

Confocal Raman microspectroscopy was used to nondestructively determine the polymorphic conversion of famotidine in the course of the milling process. A mapping system was applied to assess the blending uniformity of each polymorphic component in the milled mixture. Raman microspectroscopy combined with a thermal analyzer was also used to investigate the synergistic co‐effects of milling and heating on the polymorphic conversion of famotidine polymorphs. Famotidine has two polymorphs, forms A and B, the raw material of famotidine used was proved to be of form B. The Raman peak intensity ratio of the 2920 cm⁻¹ band for form A and 2897 cm⁻¹ band for form B was used to act as an indicator to evaluate the polymorphic conversion of famotidine form B to form A after different milling courses. The results indicate that the peak intensity at 2897 cm⁻¹ gradually decreased with the milling time, whereas the peak intensity at 2920 cm⁻¹ slowly enlarged, suggesting the polymorphic conversion of famotidine from form B to form A. The longer milling process might strongly induce and promote this polymorphic conversion of famotidine. Both polymorphic forms of famotidine were found to be well uniformly distributed within the milled samples due to their smaller varieties by using the Raman microscopic mapping system. The temperature effect could synergistically accelerate the polymorphic conversion of famotidine from form B to form A in the milled sample. The thermal‐dependent critical temperature for sharply enhancing the content of famotidine form A in each milled sample was also identified. Copyright © 2007 John Wiley & Sons, Ltd.