建筑玻璃检测

采用266 nm飞秒激光烧蚀(fLA)系统连接多集电极ICP-MS (MC-ICP-MS)，通过严格控制分析程序，获得了具有良好精度和准确性的铅同位素比值数据。266nm飞秒激光烧蚀诱导的质量分馏率约比193nm准分子激光烧蚀(eLA)诱导的质量分馏率低28%。摘要采用调优Tl比的Tl归一化指数律校正方法，获得了具有较好精度和准确度的Pb同位素数据。NIST SRM 610、612、614玻璃参考材料的Pb同位素比值;USGS bhvog - 2g、BCR-2G、GSD-1G、bir1 g;采用fa - mc - icp - ms法测定MPI-DING GOR132-G、KL2-G、T1-G、StHs60/80-G、ATHO-G、ML3B-G。在2s测量不确定度范围内，测得的铅同位素比值与参考值或公布值吻合较好。利用飞秒激光消融MC-ICP-MS分析获得了GSE- 1G、GSC-1G、GSA-1G、CGSG-1、CGSG-2、CGSG-4、CGSG-5玻璃基准材料的高精度铅同位素资料技术。

采用Ekspla公司的纳秒工业YAG激光器，型号Baltic对钠钙玻璃的微加工过程进行了研究。给出了激光加工参数和加工质量之间关系的重要信息。

The relatively clean spectrum of glass constituents enables the use of the JY 2000-2 without the need of the high resolution of the ULTIMA 2. The results show excellent agreement with expected results for all element, both major constituents and traces. The use of sequential internal standard has been shown to compensate for any viscosity differences between the samples and standards. The speed of analysis of less than 2 minutes for the 10 elements determined, and the detection limits achieved, are more than adequate for laboratories doing ordinary glass analysis. Although both acid and fusion methods were tried, afusion would appear to fulfil the requirements of full analysis in one sample preparation. If lower detection limits are required for some of the trace elements, then an HF acid digestion will be required as well.

The relatively clean spectrum of glass constituents enables the use of the JY 2000-2 without the need of the high resolution of the ULTIMA 2. The results show excellent agreement with expected results for all element, both major constituents and traces. The use of sequential internal standard has been shown to compensate for any viscosity differences between the samples and standards. The speed of analysis of less than 2 minutes for the 10 elements determined, and the detection limits achieved, are more than adequate for laboratories doing ordinary glass analysis. Although both acid and fusion methods were tried, afusion would appear to fulfil the requirements of full analysis in one sample preparation. If lower detection limits are required for some of the trace elements, then an HF acid digestion will be required as well.

The relatively clean spectrum of glass constituents enables the use of the JY 2000-2 without the need of the high resolution of the ULTIMA 2. The results show excellent agreement with expected results for all element, both major constituents and traces. The use of sequential internal standard has been shown to compensate for any viscosity differences between the samples and standards. The speed of analysis of less than 2 minutes for the 10 elements determined, and the detection limits achieved, are more than adequate for laboratories doing ordinary glass analysis. Although both acid and fusion methods were tried, afusion would appear to fulfil the requirements of full analysis in one sample preparation. If lower detection limits are required for some of the trace elements, then an HF acid digestion will be required as well.

The relatively clean spectrum of glass constituents enables the use of the JY 2000-2 without the need of the high resolution of the ULTIMA 2. The results show excellent agreement with expected results for all element, both major constituents and traces. The use of sequential internal standard has been shown to compensate for any viscosity differences between the samples and standards. The speed of analysis of less than 2 minutes for the 10 elements determined, and the detection limits achieved, are more than adequate for laboratories doing ordinary glass analysis. Although both acid and fusion methods were tried, afusion would appear to fulfil the requirements of full analysis in one sample preparation. If lower detection limits are required for some of the trace elements, then an HF acid digestion will be required as well.

The relatively clean spectrum of glass constituents enables the use of the JY 2000-2 without the need of the high resolution of the ULTIMA 2. The results show excellent agreement with expected results for all element, both major constituents and traces. The use of sequential internal standard has been shown to compensate for any viscosity differences between the samples and standards. The speed of analysis of less than 2 minutes for the 10 elements determined, and the detection limits achieved, are more than adequate for laboratories doing ordinary glass analysis. Although both acid and fusion methods were tried, afusion would appear to fulfil the requirements of full analysis in one sample preparation. If lower detection limits are required for some of the trace elements, then an HF acid digestion will be required as well.

The relatively clean spectrum of glass constituents enables the use of the JY 2000-2 without the need of the high resolution of the ULTIMA 2. The results show excellent agreement with expected results for all element, both major constituents and traces. The use of sequential internal standard has been shown to compensate for any viscosity differences between the samples and standards. The speed of analysis of less than 2 minutes for the 10 elements determined, and the detection limits achieved, are more than adequate for laboratories doing ordinary glass analysis. Although both acid and fusion methods were tried, afusion would appear to fulfil the requirements of full analysis in one sample preparation. If lower detection limits are required for some of the trace elements, then an HF acid digestion will be required as well.

The relatively clean spectrum of glass constituents enables the use of the JY 2000-2 without the need of the high resolution of the ULTIMA 2. The results show excellent agreement with expected results for all element, both major constituents and traces. The use of sequential internal standard has been shown to compensate for any viscosity differences between the samples and standards. The speed of analysis of less than 2 minutes for the 10 elements determined, and the detection limits achieved, are more than adequate for laboratories doing ordinary glass analysis. Although both acid and fusion methods were tried, afusion would appear to fulfil the requirements of full analysis in one sample preparation. If lower detection limits are required for some of the trace elements, then an HF acid digestion will be required as well.

The relatively clean spectrum of glass constituents enables the use of the JY 2000-2 without the need of the high resolution of the ULTIMA 2. The results show excellent agreement with expected results for all element, both major constituents and traces. The use of sequential internal standard has been shown to compensate for any viscosity differences between the samples and standards. The speed of analysis of less than 2 minutes for the 10 elements determined, and the detection limits achieved, are more than adequate for laboratories doing ordinary glass analysis. Although both acid and fusion methods were tried, afusion would appear to fulfil the requirements of full analysis in one sample preparation. If lower detection limits are required for some of the trace elements, then an HF acid digestion will be required as well.

The relatively clean spectrum of glass constituents enables the use of the JY 2000-2 without the need of the high resolution of the ULTIMA 2. The results show excellent agreement with expected results for all element, both major constituents and traces. The use of sequential internal standard has been shown to compensate for any viscosity differences between the samples and standards. The speed of analysis of less than 2 minutes for the 10 elements determined, and the detection limits achieved, are more than adequate for laboratories doing ordinary glass analysis. Although both acid and fusion methods were tried, afusion would appear to fulfil the requirements of full analysis in one sample preparation. If lower detection limits are required for some of the trace elements, then an HF acid digestion will be required as well.

The relatively clean spectrum of glass constituents enables the use of the JY 2000-2 without the need of the high resolution of the ULTIMA 2. The results show excellent agreement with expected results for all element, both major constituents and traces. The use of sequential internal standard has been shown to compensate for any viscosity differences between the samples and standards. The speed of analysis of less than 2 minutes for the 10 elements determined, and the detection limits achieved, are more than adequate for laboratories doing ordinary glass analysis. Although both acid and fusion methods were tried, afusion would appear to fulfil the requirements of full analysis in one sample preparation. If lower detection limits are required for some of the trace elements, then an HF acid digestion will be required as well.

玻璃通常按主要成分分为氧化物玻璃和非氧化物玻璃。非氧化物玻璃分为硫系玻璃（阴离子多为硫、硒、碲等）和卤化物玻璃；氧化物玻璃分为硅酸盐玻璃、硼酸盐玻璃、磷酸盐玻璃等。 X 荧光光谱仪对玻璃行业的进厂原料、玻璃成品的元素组成成份具有很好的分析效果。这里以 WDX 系列 X 荧光光谱仪对玻 璃行业进厂原料（石灰石、白云石）及玻璃成品的重复性测试为例，介绍玻璃行业的应用解决方案。

玻璃通常按主要成分分为氧化物玻璃和非氧化物玻璃。非氧化物玻璃分为硫系玻璃（阴离子多为硫、硒、碲等）和卤化物玻璃；氧化物玻璃分为硅酸盐玻璃、硼酸盐玻璃、磷酸盐玻璃等。 X 荧光光谱仪对玻璃行业的进厂原料、玻璃成品的元素组成成份具有很好的分析效果。这里以 WDX 系列 X 荧光光谱仪对玻 璃行业进厂原料（石灰石、白云石）及玻璃成品的重复性测试为例，介绍玻璃行业的应用解决方案。

玻璃通常按主要成分分为氧化物玻璃和非氧化物玻璃。非氧化物玻璃分为硫系玻璃（阴离子多为硫、硒、碲等）和卤化物玻璃；氧化物玻璃分为硅酸盐玻璃、硼酸盐玻璃、磷酸盐玻璃等。 X 荧光光谱仪对玻璃行业的进厂原料、玻璃成品的元素组成成份具有很好的分析效果。这里以 WDX 系列 X 荧光光谱仪对玻 璃行业进厂原料（石灰石、白云石）及玻璃成品的重复性测试为例，介绍玻璃行业的应用解决方案。荧光分析玻璃的主要成分Na

玻璃通常按主要成分分为氧化物玻璃和非氧化物玻璃。非氧化物玻璃分为硫系玻璃（阴离子多为硫、硒、碲等）和卤化物玻璃；氧化物玻璃分为硅酸盐玻璃、硼酸盐玻璃、磷酸盐玻璃等。 X 荧光光谱仪对玻璃行业的进厂原料、玻璃成品的元素组成成份具有很好的分析效果。这里以 WDX 系列 X 荧光光谱仪对玻 璃行业进厂原料（石灰石、白云石）及玻璃成品的重复性测试为例，介绍玻璃行业的应用解决方案。玻璃中Mg检测

玻璃通常按主要成分分为氧化物玻璃和非氧化物玻璃。非氧化物玻璃分为硫系玻璃（阴离子多为硫、硒、碲等）和卤化物玻璃；氧化物玻璃分为硅酸盐玻璃、硼酸盐玻璃、磷酸盐玻璃等。 X 荧光光谱仪对玻璃行业的进厂原料、玻璃成品的元素组成成份具有很好的分析效果。这里以 WDX 系列 X 荧光光谱仪对玻 璃行业进厂原料（石灰石、白云石）及玻璃成品的重复性测试为例，介绍玻璃行业的应用解决方案。玻璃中Fe检测

玻璃通常按主要成分分为氧化物玻璃和非氧化物玻璃。非氧化物玻璃分为硫系玻璃（阴离子多为硫、硒、碲等）和卤化物玻璃；氧化物玻璃分为硅酸盐玻璃、硼酸盐玻璃、磷酸盐玻璃等。 X 荧光光谱仪对玻璃行业的进厂原料、玻璃成品的元素组成成份具有很好的分析效果。这里以 WDX 系列 X 荧光光谱仪对玻 璃行业进厂原料（石灰石、白云石）及玻璃成品的重复性测试为例，介绍玻璃行业的应用解决方案。玻璃中Al检测

This application report shows that the ICP-AES is an appropriate technique for the analysis of glass samples due to the very large dynamic range. The high reproducibility of the ULTIMA was shown and enables a high throughput with less time needed for re-slope of the calibration curves. The accuracy for major elements was obtained using the internal standard.

This application report shows that the ICP-AES is an appropriate technique for the analysis of glass samples due to the very large dynamic range. The high reproducibility of the ULTIMA was shown and enables a high throughput with less time needed for re-slope of the calibration curves. The accuracy for major elements was obtained using the internal standard.

This application report shows that the ICP-AES is an appropriate technique for the analysis of glass samples due to the very large dynamic range. The high reproducibility of the ULTIMA was shown and enables a high throughput with less time needed for re-slope of the calibration curves. The accuracy for major elements was obtained using the internal standard.

This application report shows that the ICP-AES is an appropriate technique for the analysis of glass samples due to the very large dynamic range. The high reproducibility of the ULTIMA was shown and enables a high throughput with less time needed for re-slope of the calibration curves. The accuracy for major elements was obtained using the internal standard.

This application report shows that the ICP-AES is an appropriate technique for the analysis of glass samples due to the very large dynamic range. The high reproducibility of the ULTIMA was shown and enables a high throughput with less time needed for re-slope of the calibration curves. The accuracy for major elements was obtained using the internal standard.

The relatively clean spectrum of glass constituents enables the use of the JY 2000-2 without the need of the high resolution of the ULTIMA 2. The results show excellent agreement with expected results for all element, both major constituents and traces. The use of sequential internal standard has been shown to compensate for any viscosity differences between the samples and standards. The speed of analysis of less than 2 minutes for the 10 elements determined, and the detection limits achieved, are more than adequate for laboratories doing ordinary glass analysis. Although both acid and fusion methods were tried, afusion would appear to fulfil the requirements of full analysis in one sample preparation. If lower detection limits are required for some of the trace elements, then an HF acid digestion will be required as well.

The relatively clean spectrum of glass constituents enables the use of the JY 2000-2 without the need of the high resolution of the ULTIMA 2. The results show excellent agreement with expected results for all element, both major constituents and traces. The use of sequential internal standard has been shown to compensate for any viscosity differences between the samples and standards. The speed of analysis of less than 2 minutes for the 10 elements determined, and the detection limits achieved, are more than adequate for laboratories doing ordinary glass analysis. Although both acid and fusion methods were tried, afusion would appear to fulfil the requirements of full analysis in one sample preparation. If lower detection limits are required for some of the trace elements, then an HF acid digestion will be required as well.

The relatively clean spectrum of glass constituents enables the use of the JY 2000-2 without the need of the high resolution of the ULTIMA 2. The results show excellent agreement with expected results for all element, both major constituents and traces. The use of sequential internal standard has been shown to compensate for any viscosity differences between the samples and standards. The speed of analysis of less than 2 minutes for the 10 elements determined, and the detection limits achieved, are more than adequate for laboratories doing ordinary glass analysis. Although both acid and fusion methods were tried, afusion would appear to fulfil the requirements of full analysis in one sample preparation. If lower detection limits are required for some of the trace elements, then an HF acid digestion will be required as well.

The relatively clean spectrum of glass constituents enables the use of the JY 2000-2 without the need of the high resolution of the ULTIMA 2. The results show excellent agreement with expected results for all element, both major constituents and traces. The use of sequential internal standard has been shown to compensate for any viscosity differences between the samples and standards. The speed of analysis of less than 2 minutes for the 10 elements determined, and the detection limits achieved, are more than adequate for laboratories doing ordinary glass analysis. Although both acid and fusion methods were tried, afusion would appear to fulfil the requirements of full analysis in one sample preparation. If lower detection limits are required for some of the trace elements, then an HF acid digestion will be required as well.

The relatively clean spectrum of glass constituents enables the use of the JY 2000-2 without the need of the high resolution of the ULTIMA 2. The results show excellent agreement with expected results for all element, both major constituents and traces. The use of sequential internal standard has been shown to compensate for any viscosity differences between the samples and standards. The speed of analysis of less than 2 minutes for the 10 elements determined, and the detection limits achieved, are more than adequate for laboratories doing ordinary glass analysis. Although both acid and fusion methods were tried, afusion would appear to fulfil the requirements of full analysis in one sample preparation. If lower detection limits are required for some of the trace elements, then an HF acid digestion will be required as well.

The relatively clean spectrum of glass constituents enables the use of the JY 2000-2 without the need of the high resolution of the ULTIMA 2. The results show excellent agreement with expected results for all element, both major constituents and traces. The use of sequential internal standard has been shown to compensate for any viscosity differences between the samples and standards. The speed of analysis of less than 2 minutes for the 10 elements determined, and the detection limits achieved, are more than adequate for laboratories doing ordinary glass analysis. Although both acid and fusion methods were tried, afusion would appear to fulfil the requirements of full analysis in one sample preparation. If lower detection limits are required for some of the trace elements, then an HF acid digestion will be required as well.

The relatively clean spectrum of glass constituents enables the use of the JY 2000-2 without the need of the high resolution of the ULTIMA 2. The results show excellent agreement with expected results for all element, both major constituents and traces. The use of sequential internal standard has been shown to compensate for any viscosity differences between the samples and standards. The speed of analysis of less than 2 minutes for the 10 elements determined, and the detection limits achieved, are more than adequate for laboratories doing ordinary glass analysis. Although both acid and fusion methods were tried, afusion would appear to fulfil the requirements of full analysis in one sample preparation. If lower detection limits are required for some of the trace elements, then an HF acid digestion will be required as well.