Determination of main components in barite by X-ray fluorescence spectrometry with fusion sample preparation after acetic acid pretreatment
LI Dayong1, WANG Shikui*2, WANG Liang1, ZHANG Zhouwei1
1. Guizhou Central Laboratory of Geology and Mineral Resources,Guiyang 550018,China; 2. No.113 Geological Party,Guizhou Bureau of Geology and Mineral Exploration & Development,Liupanshui 553001,China
Abstract:It is of great significance to determine accurately the main components in barite for the subsequent development and utilization of barite resources. As the determination results of BaSO4 and SrSO4 by X-ray fluorescence spectrometry (XRF) are converted from the determination results of the analysis spectral lines of Ba and Sr, BaCO3 and SrCO3 in the sample will interfere with the determination of BaSO4 and BaSO4. After the carbonate components in the sample were separated by acetic acid pretreatment, the sample was determined by XRF, which successfully avoided the interference of BaCO3 and SrCO3 with BaSO4 and SrSO4. At the same time, the filter slag after acetic acid pretreatment was burned and weighed to calculate the sample loss. The sample mass loss caused by acetic acid pretreatment and burning was compensated by adding mixed flux with the same mass as the sample loss. The sample pellet was prepared by fusion sample preparation with mixed flux of lithium tetraborate and lithium metaborate. Consequently, a method for simultaneous determination of 5 components including BaSO4, Al2O3, SiO2, Fe and BaSO4 in barite was realized by XRF. The national reference material and Guizhou Provincial reference material of barite with a certain level of component content were selected to prepare the calibration curve. The determination coefficients of calibration curves were all not less than 0.999 8. The detection limit of BaSO4 was 0.128%, and detection limits for other components were in range of 0.004%-0.029%. The proposed method was applied to the analysis of barite samples. The results showed that the relative standard deviations (RSD) were not more than 0.2% when the determination results were greater than 5%. The relative standard deviations were not more than 2.0% when the determination results were not more than 5%. The relative errors(RE) were all less than the allowable limits specified in DZ/T 0130-2006 of the specification of testing quality management for geological laboratories.
李大勇, 王士魁, 王亮, 张周位. 醋酸预处理-熔融制样-X射线荧光光谱法测定重晶石中主要组分[J]. 冶金分析, 2023, 43(3): 27-33.
LI Dayong, WANG Shikui, WANG Liang, ZHANG Zhouwei. Determination of main components in barite by X-ray fluorescence spectrometry with fusion sample preparation after acetic acid pretreatment. , 2023, 43(3): 27-33.
[1] 李春阳,田升平,牛桂芝.中国重晶石矿主要矿集区及其资源潜力探讨[J].化工矿产地质,2010,32(2):75-86. LI Chunyang,TIAN Shengping,NIU Guizhi.Discussion on China barite-concentrating area and the resource potential[J].Geology of Chemical Minerals,2010,32(2):75-86. [2] 姜雅,王婷,龙涛.关于将重晶石列为战略性矿产的原则分析[J].地球学报,2021,42(2):297-302. JIANG Ya,WANG Ting,LONG Tao.Research on listing barite as a strategic mineral resource[J].Acta Geoscientica Sinica,2021,42(2):297-302. [3] 矿产资源工业要求手册编委会.矿产资源工业要求手册[M].北京:地质出版社,2014:491-496. [4] 陈思雨,刘四清,陈章鸿.我国重晶石选矿与提纯研究现状及展望[J].矿产保护与利用,2020,40(6):33-40. CHEN Siyu,LIU Siqing,CHEN Zhanghong.Present situation and outlook of barite flotation and purification in China[J].Conservation and Utilization of Mineral Resources,2020,40(6):33-40. [5] 唐书天,殷昕,尹文梅,等.X 射线荧光光谱法测定硫酸钡含量[J].中国有色冶金,2020,6(3):75-78. TANG Shutan,YIN Xin,YIN Wenmei,et al.Determination of barium sulfate content by X-ray fluorescence spectrometry[J].China Nonferrous Metallurgy,2020,6(3):75-78. [6] 陈景伟,宋江涛,陈朝阳.X射线荧光光谱法测定重晶石中的硫酸钡方法研究[J].岩矿测试,2017,36(4):382-387. CHEN Jingwei,SONG Jiangtao,CHEN Zhaoyang.Method research on determination of barium sulfate in barite by X-ray fluorescence spectrometry[J].Rock and Mineral Analysis,2017,36(4):382-387. [7] 孙杨,李冬梅,刘茜,等.X射线荧光光谱法辅助测定重晶石中的硫酸钡[J].吉林化工学院学报,2014,23(10):17-20,24. SUN Yang,LI Dongmei,LIU Qian,et al.Determination of barium sulfate in barite by X-ray fluorescence spectrometry[J].Journal of Jilin Institute of Chemical Technology,2014,23(10):17-20,24. [8] 仵利萍,刘卫.熔融制样-X 射线荧光光谱法测定重晶石中主次量元素[J].岩矿测试,2011,30(2):217-221. WU Liping,LIU Wei.Determination of major and minor elements in baryte ores by X-ray fluorescence spectrometry with fusion sample preparation[J].Rock and Mineral Analysis,2011,30(2):217-221. [9] 岩石矿物分析编委会.岩石矿物分析:第2分册[M].4版.北京:北京地质出版社,2011:351-353. [10] 吴俊,张明杰,任小荣,等.电感耦合等离子体原子发射光谱法测定重晶石中碳酸钡和硫酸钡[J].冶金分析,2017,37(12):38-44. WU Jun,ZHANG Mingjie,REN Xiaorong,et al.Determination of barium carbonate and sulfate in batite by inductively coupled plasma atomic emission spectrometry[J].Metallurgical Analysis,2017,37(12):38-44. [11] 金世兰,郑浩,曾扬,等.天青石及锶矿中硫酸锶的测定[J].干旱环境监测,2022,16(4):205-206. JIN Shilan,ZHEN Hao,ZENG Yang,et al.Determination of strontium sulfate in celestite and strontium ore[J].Arid Environmental Monitoring,2022,16(4):205-206. [12] 袁润蕾,于亚辉,刘军,等.电感耦合等离子体原子发射光谱法测定土壤中8种组分[J].冶金分析,2019,39(11): 55-61. YUAN Runlei,YU Yahui,LIU Jun,et al.Determination of eight components in soil by inductively coupled plasma atomic emission spectrometry[J].Metallurgical Analysis,2019,39(11):55-61. [13] 李大勇,贾双琳,陈菊.X射线荧光光谱法测定锰矿中主次成分技术应用研究[J].贵州地质,2015,32(4):293-297. LI Dayong,JIA Shuanglin,CHEN Ju.Application study of X-ray fluorescence spectrometry in major and minor components determination of manganese ore[J].Guizhou Geology,2015,32(4):293-297. [14] 宋祖峰,陆向东,陈海峰,等.熔融制样-X射线荧光光谱法测定磷铁中磷硅锰钛[J].冶金分析,2020,40(8):55-61. SONG Zufeng,LU Xiangdong,CHEN Haifeng,et al.Determination of phosphorus,silicon,manganese and titanium in ferrophosphorus by X-ray fluorescence spectrometry with fusion sample preparation[J].Metallurgical Analysis,2020,40(8):55-61.