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作 者:吴如云 殷晓伟 居沈贵 WU Ru-yun;YIN Xiao-wei;JU Shen-gui(College of Chemical Engineering, Nanjing Tech University, Nanjing 210009, China;Jiangsu Fangyuan Pharmaceutical Co. , Changzhou 213000, China)
机构地区:[1]南京工业大学化工学院,江苏南京210009 [2]江苏方圆制药有限公司,江苏常州213000
出 处:《应用化工》2018年第4期675-678,683,共5页Applied Chemical Industry
基 金:国家自然科学基金(U1407122);江苏省创新项目(KYLX15_0796)
摘 要:以Mn(NO_3)_2为锰源,LiOH为锂源,H_2O_2为氧化剂,采用复合法制备Li Mn_2O_4,对共沉淀、水热和煅烧三个过程进行考察。结果表明,制备LiMn_2O_4的优化条件为:H_2O_2用量1.5 m L,摩尔比n(Li/Mn)=3,水热温度为170℃,反应时间为10 h,在700℃煅烧10 h,获得的LiMn_2O_4前驱体具有最稳定结构,颗粒粒径在50 nm左右,经酸洗后得到离子筛,其吸附容量达32.4 mg/g。LiMn2O4 was successfully prepared by using Mn(NO3)2 as Mn source,Li OH as lithium source and H2O2 as oxidant. The three processes of co-precipitation,hydrothermal and calcination were investigated. The optimized experiment was carried out to prepare the ion sieve: the amount of H2O2 was 1. 5 m L,n( Li/Mn) = 3,the hydrothermal temperature was 170 ℃,the reaction time was 10 h,and the synthetic sample was calcined at 700 ℃ for 10 h. The LiMn2O4 precursor obtained after the calcination has the most stable structure,the size of which was 50 nm and the adsorption capacity reached 32. 4 mg/g after acid leaching.
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