DC-Link Capacitor Optimization in AC–DC Converter by Load Current Prediction

Alternating Current–Direct Current(AC–DC)converters require a high value bulk capacitor or afilter capacitor between the DC–DC conversion stages,which in turn causes many problems in the design of a AC–DC converter.The component package size for this capacitor is large due to its high voltage rating and capacitance value.In addition,the high charging current creates more pro-blems during the product compliance testing phase.The shelf life of these specific high value capacitors is less than that of Multilayer Ceramic Capacitors(MLCC),which limits its use for the highly reliable applications.This paper presents a fea-sibility study to overcome these two problems by adding a few sensing mechan-isms to the typical AC–DC converter topology.In majority of the AC–DC converter,Al-Elko capacitor takes approximately 3%to 5%of the converter size.The proposed method reduces this to approximately 50%size and so it effectively approximates 2%to 3%size reduction in converter size.The proposed method basically works based on the load current prediction method and hence it is highly suitable for the constant load application.Moreover,the converter response time increases in this method,which limit its application in high-speed systems.The high temperature application of Al-Elko capacitor is limited because of its poor performance,which is significantly rectified by replacing the Al-Elko with MLCC as it delivers good performance in high temperature.

Removing aluminum from a low-concentration lixivium of weathered crust elution-deposited rare earth ore with neutralizing hydrolysis

Aluminum,the main impurity in the lixivium of weathered crust elution deposited rare earth ore,not only results in an increasing consumption of precipitant in the rare earth precipitation process,but also lowers the purity of final rare earth product.Aluminum in the weathered crust elution-deposited rare earth ore lixivium should be removed.Neutralizing hydrolysis method was employed to remove aluminum from the lixivium.Hexamethylenetetramine was found to be the optimum pH regulator for the removal of aluminum in the low concentration.When used to adjust the pH value of the lixivium to 5.0,aluminum in the lixivium can be effectively removed in the form of aluminum hydroxide precipitation with removal rate of 97.60%.It shows that hexamethylenetetramine has a good effect on the removing of aluminum ions from the lowconcentration lixivium.Moreover,hexamethylenetetramine in removing aluminum from lixivium has little adverse effect on the RE precipitation process.

Fluoride removal by Al,Ti,and Fe hydroxides and coexisting ion effect

Batch experiments were conducted to evaluate fluoride removal by Al,Fe,and Ti-based coagulants and adsorbents,as well as the effects of coexisting ions and formation of aluminum–fluoride complexes on fluoride removal by co-precipitation with alum（Al_2（SO_4）_3·18H_2O）.Aluminum sulfate was more efficient than the other coagulants for fluoride removal in the pH range between 6 and 8.Nano-crystalline TiO_2 was more effective for fluoride removal than Al and Fe hydroxides in a pH range of 3–5.Coexisting anions in water decreased the removal of fluoride in the order：phosphate（2.5 mg/L） 〉 arsenate（0.1 mg/L） 〉 bicarbonate（200 mg/L） 〉sulfate（100 mg/L） = nitrate（100 mg/L） 〉 silicate（10 mg/L） at a pH of 6.0.The effect of silicate became more significant at pH 〉 7.0.Calcium and magnesium improved the removal of fluoride.Zeta-potential measurements determined that the adsorption of fluoride shifted the PZC of Al（OH）_3 precipitates from 8.9 to 8.4,indicating the chemical adsorption of fluoride at the surface.The presence of fluoride in solution significantly increased the soluble aluminum concentration at pH 〈 6.5.A Visual MINTEQ modeling study indicated that the increased aluminum solubility was caused by the formation of AlF^（2＋）,AlF^（＋2）,and AlF_3complexes.The AlF_x complexes decreased the removal of fluoride during co-precipitation with aluminum sulfate.