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Preparation and characteristic research of anhydrous magnesium chloride with dehydrated ammonium carnallite

机译:脱水铵盐红岩制备无水氯化镁及其特性研究

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Taking the saline lake bischofite and NH4Cl that was removed with the ammonia method and continuwas synthesized. And then the ammonium carnallite was dehydrated to some extent at 160℃ for 4 h. Ammonium carnallite reacted with ammonia at 240℃ for 150 min and the ammonation ammonium carnallite was produced. Finally, the ammonation ammonium carnallite was calcined at 750℃ into anhydrous magnesium chloride containing only 0.1% (mass fraction) of MgO. On the other hand, dehydrated ammonium carnallite was mixed with the solid ammonium chloride at mass ratio 1:4 at high temperature and with the differential pressure of HN3 above 30.5 kPa. The dehydrated ammonium carnallite of mixture was dehydrated at 410℃, and then calcined at 700℃ into anhydrous magnesium chloride with only 0. 087% (mass fraction) of MgO. X-ray diffraction and electron microscopy analysis results prove that anhydrous magnesium chloride obtained by both methods hasn't mixed phases, the particle is large and even has good dispersion, which is suitable for preparation of metal magnesium in the electrolysis.
机译:取盐湖重铬铁矿和氨水法脱除的NH4Cl,继续合成。然后在160℃下将香石碱铵脱水至一定程度4小时。氨水钠盐在240℃下与氨反应150min,制得氨化水钠盐。最后,将氨化钠盐钠盐在750℃煅烧成仅含有0.1%(质量分数)MgO的无水氯化镁。另一方面,在高温和HN3的压差高于30.5 kPa的条件下,将脱水铵盐卤钠盐与固体氯化铵以质量比1:4混合。混合物的脱水铵盐卤钠盐在410℃下脱水,然后在700℃下煅烧成仅含0. 087%(质量分数)MgO的无水氯化镁。 X射线衍射和电子显微镜分析结果表明,两种方法制得的无水氯化镁没有混合相,颗粒大,分散性好,适用于电解制备金属镁。

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