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副產硫酸鈣室溫固相球磨制備氧化鈣

Preparation of calcium oxide from by-product calcium sulfate by solid-state ball milling reaction at ambient temperature

  • 摘要: 以錳尾礦制備硫酸錳過程中副產硫酸鈣為原料在室溫下與碳酸氫銨進行固相球磨反應,制備出氧化鈣的前驅體碳酸鈣,然后將其煅燒得到氧化鈣.分別考察了物料配比、球磨時間、球料質量比等因素對硫酸鈣轉化率的影響,采用X射線衍射和化學分析方法對產物進行了分析,并對室溫固相球磨反應的機理進行了探討.在物料配比(摩爾比)為3.5:1、球磨時間為40 min以及球料質量比為5:1時,硫酸鈣的轉化率可達到99.8%,將固相產物在1000℃熱解1 h后所制備的氧化鈣純度為99.2%.室溫球磨過程細化了反應物的顆粒尺寸,增加了反應物的接觸面積,為引發反應提供了必要的能量,因此提高了化學反應的有效性.

     

    Abstract: Calcium oxide(CaO) was prepared by directly pyrolyzing the precursor called calcium carbonate (CaCO3),which was synthesized by solid-state ball milling reaction between NH4HCO3 and CaSO4·2H2O,the byproduct generated during the preparation of MnSO4.The effects of NH4HCO3-to-CaSO4·2H2O molar ratio,milling time,and ball-to-feed mass ratio on the conversion of CaSO4·2H2O were investigated respectively.The product was analyzed by X-ray diffraction and chemical analytical method.The reaction mechanism was also discussed.When the NH4HCO3-to-CaSO4·2H2O molar ratio is 3.5:1,the milling time is 40 min,and the ball-to-feed mass ratio is 5:1,the conversion rate of CaSO4·2H2O reaches 99.8%.Calcium oxide,whose purity is 99.2%,can be prepared by pyrolyzing the precursor at 1000℃for 1 h.The effectiveness of the solid-state reaction is improved by refining the reactant size, increasing the contact area,and providing necessary energy during the ball-milling process at ambient temperature.

     

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