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机构地区:[1]山西太钢不锈钢股份有限公司技术中心,山西太原030003
出 处:《冶金分析》2016年第7期79-82,共4页Metallurgical Analysis
摘 要:采用盐硝混合酸(1+1+1)溶解样品,通过选择27 Al作为测定用同位素和设置中分辨率(R=4 000)消除质谱干扰,以标准加入法绘制校准曲线消除基体效应,避免了对样品基体进行分离的繁琐前处理过程,实现了电感耦合等离子体质谱法(ICP-MS)对铁基非晶合金中痕量铝的测定。实验表明,称取0.100 0g样品于石英三角瓶中,准确加入10.0 mL盐硝混合酸(1+1+1),电热板上低温加热可将样品完全溶解;采用标准加入法建立校准曲线,相关系数为0.999 0,线性范围为0.000 1%~0.005 0%,方法的检出限为0.035μg/g。按照实验方法,对2个铁基非晶合金样品中痕量铝进行测定,测得结果的相对标准偏差(RSD,n=9)为6.1%~7.1%,回收率为96%~106%。将实验方法与电感耦合等离子体原子发射光谱法(ICP-AES)进行方法比对,两种方法对铁基非金合金实际样品中铝的测定结果基本一致。The sample was dissolved with mixed hydrochloric acid and nitric acid(1+1+1).The mass spectrometry interference was eliminated by selecting 27 Al as determination isotope and setting moderate resolution(R=4 000).The calibration curve was prepared by standard addition method to avoid the matrix effect as well as complicated pretreatment process of matrix separation.Thus,the determiantion of trace aluminum in iron-based amorphous alloy was realized by inductively coupled plasma mass spectrometry(ICP-MS).The results showed that 0.100 0g of sample could be fully dissolved in quartz triangular flask by low temperature heating on electric hot plate with 10.0mL of hydrochloric acid-nitric acid(1+1+1)as solvent.The calibration curve was established by standard addition method with correlation coefficient as 0.999 0and linear range of 0.000 1%-0.005 0%.The detection limit of method was 0.035μg/g.The experimental method was applied to the determination of trace aluminum in two iron-based amorphous alloy samples.The relative standard deviations(RSD,n=9)were between 6.1% and 7.1%,and the recoveries were between 96%and 106%.This proposed method was compared with inductively coupled plasma atomic emission spectrometry(ICP-AES),and the determination results of trace aluminum in actual iron-based amorphous alloy sample were consisit.
关 键 词:电感耦合等离子体质谱法(ICP-MS) 铁基非晶合金 铝
分 类 号:TG115.33[金属学及工艺—物理冶金]
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