广东微量元素科学
廣東微量元素科學
엄동미량원소과학
GUANGDONG TRACE ELEMENTS SCIENCE
2014年
8期
23-28
,共6页
梁群珍%李元尊%王生%肖国军
樑群珍%李元尊%王生%肖國軍
량군진%리원존%왕생%초국군
饮用水%金属元素%快速检测%ICP-MS法
飲用水%金屬元素%快速檢測%ICP-MS法
음용수%금속원소%쾌속검측%ICP-MS법
drinking water%metal elements%rapid determine%ICP-MS
目的:建立了电感耦合等离子体质谱法( ICP-MS)同时测定饮用水中铝、铜、锌、硒、砷、汞、镉、铅、铁、锰、钼、锡、铍、锑、镍、钡、银、铬、铊等19种金属元素含量的快速检测方法。方法对仪器工作参数进行优化,选取7 Li,45 Sc,72 Ge,115 In,209 Bi作为测定元素的内标元素,有效克服了基体效应、接口效应及仪器波动所产生的影响,利用八极杆碰撞/反应池技术,消除多原子离子对待测元素的干扰。结果19种金属元素在测定的含量范围内标准曲线线性关系良好,相关系数都在0.9992以上,方法检出限为0.002~0.444μg/L,定量限为0.006~1.480μg/L,低、中、高含量水样加标回收率为85.9%~105.5%,相对标准偏差( RSD)为0.60%~5.65%( n=6)。结论该法具有操作简便、干扰少、分析速度快、灵敏度高、结果准确可靠等优点,是测定饮用水中金属元素含量的理想方法。
目的:建立瞭電感耦閤等離子體質譜法( ICP-MS)同時測定飲用水中鋁、銅、鋅、硒、砷、汞、鎘、鉛、鐵、錳、鉬、錫、鈹、銻、鎳、鋇、銀、鉻、鉈等19種金屬元素含量的快速檢測方法。方法對儀器工作參數進行優化,選取7 Li,45 Sc,72 Ge,115 In,209 Bi作為測定元素的內標元素,有效剋服瞭基體效應、接口效應及儀器波動所產生的影響,利用八極桿踫撞/反應池技術,消除多原子離子對待測元素的榦擾。結果19種金屬元素在測定的含量範圍內標準麯線線性關繫良好,相關繫數都在0.9992以上,方法檢齣限為0.002~0.444μg/L,定量限為0.006~1.480μg/L,低、中、高含量水樣加標迴收率為85.9%~105.5%,相對標準偏差( RSD)為0.60%~5.65%( n=6)。結論該法具有操作簡便、榦擾少、分析速度快、靈敏度高、結果準確可靠等優點,是測定飲用水中金屬元素含量的理想方法。
목적:건립료전감우합등리자체질보법( ICP-MS)동시측정음용수중려、동、자、서、신、홍、력、연、철、맹、목、석、피、제、얼、패、은、락、사등19충금속원소함량적쾌속검측방법。방법대의기공작삼수진행우화,선취7 Li,45 Sc,72 Ge,115 In,209 Bi작위측정원소적내표원소,유효극복료기체효응、접구효응급의기파동소산생적영향,이용팔겁간팽당/반응지기술,소제다원자리자대대측원소적간우。결과19충금속원소재측정적함량범위내표준곡선선성관계량호,상관계수도재0.9992이상,방법검출한위0.002~0.444μg/L,정량한위0.006~1.480μg/L,저、중、고함량수양가표회수솔위85.9%~105.5%,상대표준편차( RSD)위0.60%~5.65%( n=6)。결론해법구유조작간편、간우소、분석속도쾌、령민도고、결과준학가고등우점,시측정음용수중금속원소함량적이상방법。
Objective To establish a rapid determination method of 19 metal elements in drinking water by ICP-MS.Methods Optimizing the operating parameters of instrument , The 7 Li, 45 Sc, 72 Ge, 115 In, 209 Bi were chosen as internal standard elements so that the effect of matrix , interface and instrument fluctuation was overcome effectively , collision/reaction technology was used to eliminate the interference because of more atomic ion . Results Satisfactory linearity of working curves of 19 elements was obtained , the correlation coefficients were all more than 0.999 2 , detection limits were between 0.002~0.444 μg/L, the RSD of parallel samples were between 0.60%to 5.65% ( n=6 ) , spiked recoveries of samples were between 85.9%to 105.5%.Conclusion The method is simple, quick, less interference, sensitive and accurate , it can be used as perfect method to determine metal elements content in drinking water.