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粉末压片-X射线荧光光谱法测定过磷酸钙中氟

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测定过磷酸钙中氟含量,对过磷酸钙生产及质量控制有指导意义.实验将样品充分干燥后粉碎至粒度小于74 μm,采用硼酸镶边,在压力35 t条件下保压30 s,制成样片,选择F-Ka线为分析线,建立了粉末压片-波长色散X射线荧光光谱法(WDXRF)测定过磷酸钙中氟的方法.采用X射线衍射(XRD)对大量过磷酸钙样品进行扫描,结果发现,过磷酸钙中物相组成主要是硫酸钙、氟化钙、二氧化硅,故实验选择以离子选择电极法定值的过磷酸钙样品为基体,加入不同质量的氟化钙后用三维混样仪混匀,配制得到一组氟含量呈一定梯度且能覆盖样品中氟含量范围的系列校准样品用于绘制校准曲线,以使校准样品系列和过磷酸钙样品中氟的谱峰角度始终保持一致,且减少了基体效应、矿物效应等对测定的影响;选取3个不同氟含量的校准样品,用三维混样仪混匀5 min后按照实验方法平行测量5次,氟荧光强度测定结果的相对标准偏差(RSD,n=5)小于3.0%,表明校准样品均匀性满足实验要求.以氟含量为横坐标,对应的氟荧光强度为纵坐标绘制校准曲线,其线性相关系数为0.999 6,方法检出限为3 mg/kg.采用实验方法对3个不同氟含量的过磷酸钙样品中氟进行测定,结果的相对标准偏差(n=10)为1.4%~3.1%;采用氟离子选择电极法对这3个样品进行测定以进行方法比对,结果表明,两种方法测定结果基本一致.
Determination of fluorine in calcium superphosphate by X-ray fluorescence spectrometry with powder pellet preparation
The determination of fluorine content in calcium superphosphate has guiding significance for the production and quality control of calcium superphosphate.In experiments,the samples were thoroughly dried and then crushed until the particle size was less than 74 μm.Boric acid was used for edging,and the sample was prepared at pressure of 35 t for 30 s.F-Kα was selected as the analytical line.The method for the determination of fluorine in calcium superphosphate by wavelength dispersive X-ray fluorescence spec-trometry(WDXRF)with powder pellet preparation was established.A large number of calcium superphos-phate samples were scanned by X-ray diffraction(XRD).The results showed that the phases in calcium su-perphosphate were mainly composed of calcium sulfate,calcium fluoride,and silicon dioxide.Therefore,the calcium superphosphate sample which was certified by ion selective electrode method was use as the matrix in experiments.Various amounts of calcium fluoride were added followed by uniform mixing using a three-dimensional sample mixer.A series of calibration samples with a certain gradient of fluorine content that could cover the range of fluorine content in the sample were obtained for the drawing of calibration curves.Therefore,the spectrum peak angles of fluorine in the calibration sample series and calcium superphosphate sample were always consistent.Moreover,the influence of matrix effect and mineral effect on the determi-nation could be reduced.Three calibration samples with different fluorine contents were selected and then mixed with a three-dimensional sample mixer for 5 min.The samples were determined in parallel for five times according to the experimental method.The results showed that the relative standard deviation(RSD,n=5)of the measurement values of fluorescence intensity was less than 3.0%,indicating that the uniform-ity of the calibration samples could meet the experimental requirements.The calibration curve of fluorine was prepared using the fluorine content as the horizontal axis and the corresponding fluorescence intensity as the vertical axis.The linear correlation coefficient was 0.999 6,and the limit of detection was 3 mg/kg.Three calcium superphosphate samples with different fluorine contents were determined according to the experimental method,and the RSDs(n=10)were between 1.4%and 3.1%.Three samples were also de-termined by fluoride ion selective electrode method for comparison.The results showed that the determina-tion values of two methods were basically consistent.

wavelength dispersive X-ray fluorescence spectrometry(WDXRF)calcium superphosphateflu-orinecalcium fluoridematrix effect

刘林、王勇、邵国庆、施宗友

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攀西钒钛检验检测院,国家钒钛制品质量检验检测中心,四川攀枝花 617000

波长色散X射线荧光光谱法(WDXRF) 过磷酸钙 氟化钙 基体效应

四川省市场监管科研项目

SCSJS2023008

2024

冶金分析
中国钢研科技集团有限公司(钢铁研究总院) 中国金属学会

冶金分析

CSTPCD北大核心
影响因子:1.124
ISSN:1000-7571
年,卷(期):2024.44(4)
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