摘要
本文以CeCl_3·7H_2O、Eu_2O_3、C_2H_2O_4·2H_2O为原料,制备了铈铕草酸盐沉淀,该沉淀经高温煅烧获得铈铕氧化物前驱体;以Ar气为载气、CS_2为硫源对铈铕氧化物前驱体进行硫化合成了Eu^(2+)掺杂的γ-Ce_2S_3。Eu^(2+)掺杂能够明显降低γ-Ce2S3的合成温度,Eu^(2+)/Ce^(3+)为0. 03时,在900℃硫化150min即可获得纯相的γ-Ce_2S_3,与不掺杂时合成γ-Ce_2S_3的温度相比降低了300℃左右;同时,Eu^(2+)掺杂能够提升γ-Ce_2S_3的抗氧化能力,氧化气氛下,Eu^(2+)/Ce^(3+)比例为0. 03的样品其氧化放热峰温度由不掺杂时的490. 6℃提高至553. 3℃。
In this paper,CeCl3·7H2O,Eu2O3 and C2H2O4·2H2O were used as raw materials to prepare europium-doped cerium oxalate by oxalate coprecipitation process.The europium-doped cerium oxalate was calcined into europium-doped cerium oxide precursor.This precursor was vulcanized into europium-dopedγ-Ce2S3 by CS2 with Ar as the carrier gas.The results showed that using Eu2+ion doping can lower the synthesis temperature and improve the temperature stability of europium-dopedγ-Ce2S3.When the ratio of Eu2+and Ce3+was 0.03,the pure phase ofγ-Ce2S3 can be obtained by vulcanized at 900℃for 150 min.The synthesis temperature ofγ-Ce2S3 had decreased by 300℃than that of pureγ-Ce2S3,and the oxidation exothermic peak of europium-dopedγ-Ce2S3 increases from490.6℃to 553.3℃.
作者
王竹梅
马振国
李月明
高轶群
宋福生
沈宗洋
李志科
Wang Zhumei;Ma Zhenguo;Li Yueming;Gao Yiqun;Song Fusheng;Shen Zongyang;Li Zhike(School of Materials Science and Engineering,Jingdezhen Ceramic Institute,China National Light Industry Key Laboratory of Functional Ceramic Materials,Energy Storage and Conversion Ceramic Materials Engineering Laboratory of Jiangxi Province,Jingdezhen 333403)
出处
《化学通报》
CAS
CSCD
北大核心
2019年第5期441-445,共5页
Chemistry
基金
江西省自然科学基金项目(2017ACB20022)
江西省教育厅科技项目(GJJ181527)
景德镇市科技计划项目(2017GYZD019-012)资助