Lithium separation technique for three reference materials has been established together with precise determination of lithium isotope using a Neptune multi collector-inductively coupled plasma mass spectrometry (MC-...Lithium separation technique for three reference materials has been established together with precise determination of lithium isotope using a Neptune multi collector-inductively coupled plasma mass spectrometry (MC-ICP-MS). The solutions of lithium element standard reference materials, potassium, calcium, sodium, magnesium and iron single element, were used to evaluate analytical methods applied. Three separate stages of ion-exchange chromatography were carried out using organic cation-exchange resin (AG 50W-X8). Lithium was enriched for the three stages using different eluants, which are 2.8 M HCl, 0.15 M HCl and 0.5 M HCl in 30% ethanol, respectively. The columns for the first and second stages are made of polypropylene, and those for the third stage are made of quartz. Total reagent volume for the entire chemical process was 35 mL for three reference materials. The recovery yielded for the three stages is 98.9-101.2% with an average of 100.0%, 97.6-101.9% with an average of 99.9%, and 99.8-103.3% with an average of 100.6%, respectively. The precision of this technique is conservatively estimated to be ±0.72-1.04‰ (2σ population), which is similar to the precision obtained by different authors in different laboratories with MC-ICP-MS. The δ7 Li values ( 7 Li/ 6 Li relative to the IRMM-016 standard) determined for andesite (AGV-2) and basalt (BHVO-2) are 5.68‰ (n=18), 4.33‰ (n=18), respectively. The δ7 Li value ( 7Li/6Li relative to the L-SVEC standard) determined for IRMM-016 is -0.01‰ (n=15). All these analytical results are in good agreement with those previously reported. In addition, the results for the same kinds of samples analyzed at the MLR Key Laboratory of Metallogeny and Mineral Assessment, Institute of Mineral Resources, Chinese Academy of Geological Sciences, are consistent with those obtained at the Plasma Laboratory, University of Maryland, within analytical uncertainty. According to these experiment results, it is concluded that this proposed procedure is a suitable method for determining the lithium isotopic composition of natural samples.展开更多
目的建立深圳市龙华人民医院院检验科丙氨酸氨基转移酶(ALT)检测系统的溯源性,提高最终检测结果的准确性。方法依据《GB/T 21415-2008/ISO 17511:2003》中的国际标准溯源链式图自建该医院检验科溯源流程图;购买参考物质IRMM ERM AD 454...目的建立深圳市龙华人民医院院检验科丙氨酸氨基转移酶(ALT)检测系统的溯源性,提高最终检测结果的准确性。方法依据《GB/T 21415-2008/ISO 17511:2003》中的国际标准溯源链式图自建该医院检验科溯源流程图;购买参考物质IRMM ERM AD 454,通过测定临床新鲜血清标本进行临床比对确保参考物质具有互通性,同时采用SPSS17.0进行统计学分析,以97%的预测区间和检测项目1/4CL IA'88总允许误差为标准,达到量值传递验证要求,进一步确定不确定度,完成量值溯源工作。结果通过该医院自建的溯源流程实验,证明丙氨酸氨基转移酶试剂盒的产品校准品与IRMM ERM AD 454之间存在互通性,按照不确定度计算公式得到产品校准品的不确定度,赋值表示为135±5U/L。结论该医院检验科自建溯源流程成功对产品校准品进行了赋值修正,提高了试剂检测结果的准确性。展开更多
基金supported by grants from the Natural Science Foundation of China (no. 40973013,41173003)the Ministry of Land and Resources (no.201011027)+2 种基金China Geological Survey (no.1212011120298, 1212010816027)the Ministry of Science and Technology (no. K0802)the Open Foundation of Chinese Academy of Geological Sciences (no. 2009-SYS-06)
文摘Lithium separation technique for three reference materials has been established together with precise determination of lithium isotope using a Neptune multi collector-inductively coupled plasma mass spectrometry (MC-ICP-MS). The solutions of lithium element standard reference materials, potassium, calcium, sodium, magnesium and iron single element, were used to evaluate analytical methods applied. Three separate stages of ion-exchange chromatography were carried out using organic cation-exchange resin (AG 50W-X8). Lithium was enriched for the three stages using different eluants, which are 2.8 M HCl, 0.15 M HCl and 0.5 M HCl in 30% ethanol, respectively. The columns for the first and second stages are made of polypropylene, and those for the third stage are made of quartz. Total reagent volume for the entire chemical process was 35 mL for three reference materials. The recovery yielded for the three stages is 98.9-101.2% with an average of 100.0%, 97.6-101.9% with an average of 99.9%, and 99.8-103.3% with an average of 100.6%, respectively. The precision of this technique is conservatively estimated to be ±0.72-1.04‰ (2σ population), which is similar to the precision obtained by different authors in different laboratories with MC-ICP-MS. The δ7 Li values ( 7 Li/ 6 Li relative to the IRMM-016 standard) determined for andesite (AGV-2) and basalt (BHVO-2) are 5.68‰ (n=18), 4.33‰ (n=18), respectively. The δ7 Li value ( 7Li/6Li relative to the L-SVEC standard) determined for IRMM-016 is -0.01‰ (n=15). All these analytical results are in good agreement with those previously reported. In addition, the results for the same kinds of samples analyzed at the MLR Key Laboratory of Metallogeny and Mineral Assessment, Institute of Mineral Resources, Chinese Academy of Geological Sciences, are consistent with those obtained at the Plasma Laboratory, University of Maryland, within analytical uncertainty. According to these experiment results, it is concluded that this proposed procedure is a suitable method for determining the lithium isotopic composition of natural samples.
文摘目的建立深圳市龙华人民医院院检验科丙氨酸氨基转移酶(ALT)检测系统的溯源性,提高最终检测结果的准确性。方法依据《GB/T 21415-2008/ISO 17511:2003》中的国际标准溯源链式图自建该医院检验科溯源流程图;购买参考物质IRMM ERM AD 454,通过测定临床新鲜血清标本进行临床比对确保参考物质具有互通性,同时采用SPSS17.0进行统计学分析,以97%的预测区间和检测项目1/4CL IA'88总允许误差为标准,达到量值传递验证要求,进一步确定不确定度,完成量值溯源工作。结果通过该医院自建的溯源流程实验,证明丙氨酸氨基转移酶试剂盒的产品校准品与IRMM ERM AD 454之间存在互通性,按照不确定度计算公式得到产品校准品的不确定度,赋值表示为135±5U/L。结论该医院检验科自建溯源流程成功对产品校准品进行了赋值修正,提高了试剂检测结果的准确性。