Uneven distribution of minor metals and migration of isotopes in polymeric material （polypropylene） - originating under certain physical and chemical conditions-could possibly affect the stability and bio-compatibil...Uneven distribution of minor metals and migration of isotopes in polymeric material （polypropylene） - originating under certain physical and chemical conditions-could possibly affect the stability and bio-compatibility of such material. Unusually high levels of embedded surface metal isotopes from migration effects could affect studies such as tissue engineering and biospecific adhesion of cells to polymeric surfaces. There is, therefore, a general need to know the distribution of metal isotopes in such polymeric materials. We have developed an ultrasensitive technique for assessing the isotopic distribution in polymer matrices, and studying migration of metal isotopes. The technique uses laser ablation linked to an ICP-MS instrument. It is semi-quantitative and capable of high-resolution detection over a wide range of elemental levels. Polymers usually contain catalytic residues and other minor metal impurities. Some of the isotopes of these metals migrate to the surface, while others remain embedded deep in the polymeric product. Such unwanted metallic residues and isotopes could be a potential hazard, and ablative laser technology has the ability to study homogeneity of such distributions in the polymer matrix. The aim of this paper, therefore, is to explore the potential of our method for studying isotope migration using suitable polypropylene samples.展开更多
Depth profiling studies (laser ICP-MS) of ions (Cl-, Na+, Mg2+) in concrete-based material can be used to provide useful information on the migration paths of these ionic species. In particular, deterioration of concr...Depth profiling studies (laser ICP-MS) of ions (Cl-, Na+, Mg2+) in concrete-based material can be used to provide useful information on the migration paths of these ionic species. In particular, deterioration of concrete through infiltration of chloride could lead to costly corrosion problems with serious impact on the environment. Many modeling studies on concrete matrices depend on the tortuosity of these transport paths. Our work showed that dispersion paths of ionic species in concrete are intermittent and sporadic, suggesting that applications of simplifying assumptions in treatment of such data could lead to appreciable perturbations in related mathematical models. This paper examines the capability of using a high resolution ICP-MS laser ablation technique to track Cl– migration in concrete samples in the presence of other ions such as Na+ and Mg2+. Cationic migration in such materials is underexplored and data in this particular area could contribute to modeling studies. Concrete bricks (with and without surface coatings) were specially prepared in cubic configurations and allowed to saturate in a ponding medium (sea water). The study subsequently examined the distribution of Cl– , Na+ and Mg2+ with depth in protected (epoxy coated) and unprotected cored concrete slivers (5 mm diameter;2 mm thick) using an 80 μm- diameter laser beam coupled to an ICP-MS instrument. The laser (213 nm) was programmed to ablate a total depth of 50 μm at each point at 5-μm intervals. The results in unprotected samples indicated that chloride intensity showed a general decline with depth, suggesting that mobility of the chloride is a function of its interaction with the concrete matrix. In some cases ‘hotspots’ were observed at certain points indicating that transport of the intruding ion was limited. No significant mobility was observed in coated samples. The depth-profiling results for Na+ and Mg2+ were somewhat unexpected. Strong similarities in their spectra purported that the matrix was indifferent to charge and size of the ion. Our experimental data further showed that the matrix itself offers natural protection to the reinforced steel rebars by limiting chloride and metal diffusion at certain locations. Clearly, if the composition of these protective environments within the concrete could be simulated on a larger scale and introduced into the matrix it would offer scope for extended research in this area. Our work would be of definite interest to materials and environmental research;and mechanistic studies on aggregates.展开更多
目的 建立电感耦合等离子体质谱法(inductively coupled plasma-mass spectrometry,ICP-MS)测定注射用亚锡甲氧异腈中元素杂质的含量。方法 样品溶解后,采用ICP-MS半定量测定模式对注射用亚锡甲氧异腈中元素杂质进行初步筛查,结合国际...目的 建立电感耦合等离子体质谱法(inductively coupled plasma-mass spectrometry,ICP-MS)测定注射用亚锡甲氧异腈中元素杂质的含量。方法 样品溶解后,采用ICP-MS半定量测定模式对注射用亚锡甲氧异腈中元素杂质进行初步筛查,结合国际人用药品注册技术协调会(International Council for Harmonisation of Technical Requirements for Pharmaceuticals for Human Use,ICH)Q3D元素杂质指导原则的要求,确定16种元素:锂(Li)、镁(Mg)、铝(Al)、硅(Si)、钾(K)、钒(V)、铁(Fe)、钴(Co)、镍(Ni)、锌(Zn)、砷(As)、镉(Cd)、铟(In)、锑(Sb)、汞(Hg)和铅(Pb)作为定量考察和控制的元素杂质研究对象。ICP-MS采集模式选择动能歧视模式进行定量方法研究,分别以钪(Sc)、锗(Ge)、钇(Y)、铋(Bi)作为内标,测定16种元素杂质的含量。结果 16种元素杂质在各自线性范围内响应与浓度相关性良好(r≥0.999 3);方法精密度(RSD≤3.53%)和重复性(RSD≤3.69%)均较好;各元素平均回收率为95.86%~105.64%(RSD≤5.06%,n=9),方法准确性良好。注射用亚锡甲氧异腈样品中16种元素均未超出限度,Mg、K、Zn 3种元素含量相对较高。结论 金属盐类制剂产品可能引入ICH Q3D原则要求以外的元素杂质。本研究建立的ICP-MS定量方法简便、快速,可用于注射用亚锡甲氧异腈中元素杂质的筛查、检测和风险评估。展开更多
文摘Uneven distribution of minor metals and migration of isotopes in polymeric material （polypropylene） - originating under certain physical and chemical conditions-could possibly affect the stability and bio-compatibility of such material. Unusually high levels of embedded surface metal isotopes from migration effects could affect studies such as tissue engineering and biospecific adhesion of cells to polymeric surfaces. There is, therefore, a general need to know the distribution of metal isotopes in such polymeric materials. We have developed an ultrasensitive technique for assessing the isotopic distribution in polymer matrices, and studying migration of metal isotopes. The technique uses laser ablation linked to an ICP-MS instrument. It is semi-quantitative and capable of high-resolution detection over a wide range of elemental levels. Polymers usually contain catalytic residues and other minor metal impurities. Some of the isotopes of these metals migrate to the surface, while others remain embedded deep in the polymeric product. Such unwanted metallic residues and isotopes could be a potential hazard, and ablative laser technology has the ability to study homogeneity of such distributions in the polymer matrix. The aim of this paper, therefore, is to explore the potential of our method for studying isotope migration using suitable polypropylene samples.
文摘Depth profiling studies (laser ICP-MS) of ions (Cl-, Na+, Mg2+) in concrete-based material can be used to provide useful information on the migration paths of these ionic species. In particular, deterioration of concrete through infiltration of chloride could lead to costly corrosion problems with serious impact on the environment. Many modeling studies on concrete matrices depend on the tortuosity of these transport paths. Our work showed that dispersion paths of ionic species in concrete are intermittent and sporadic, suggesting that applications of simplifying assumptions in treatment of such data could lead to appreciable perturbations in related mathematical models. This paper examines the capability of using a high resolution ICP-MS laser ablation technique to track Cl– migration in concrete samples in the presence of other ions such as Na+ and Mg2+. Cationic migration in such materials is underexplored and data in this particular area could contribute to modeling studies. Concrete bricks (with and without surface coatings) were specially prepared in cubic configurations and allowed to saturate in a ponding medium (sea water). The study subsequently examined the distribution of Cl– , Na+ and Mg2+ with depth in protected (epoxy coated) and unprotected cored concrete slivers (5 mm diameter;2 mm thick) using an 80 μm- diameter laser beam coupled to an ICP-MS instrument. The laser (213 nm) was programmed to ablate a total depth of 50 μm at each point at 5-μm intervals. The results in unprotected samples indicated that chloride intensity showed a general decline with depth, suggesting that mobility of the chloride is a function of its interaction with the concrete matrix. In some cases ‘hotspots’ were observed at certain points indicating that transport of the intruding ion was limited. No significant mobility was observed in coated samples. The depth-profiling results for Na+ and Mg2+ were somewhat unexpected. Strong similarities in their spectra purported that the matrix was indifferent to charge and size of the ion. Our experimental data further showed that the matrix itself offers natural protection to the reinforced steel rebars by limiting chloride and metal diffusion at certain locations. Clearly, if the composition of these protective environments within the concrete could be simulated on a larger scale and introduced into the matrix it would offer scope for extended research in this area. Our work would be of definite interest to materials and environmental research;and mechanistic studies on aggregates.
文摘目的 建立电感耦合等离子体质谱法(inductively coupled plasma-mass spectrometry,ICP-MS)测定注射用亚锡甲氧异腈中元素杂质的含量。方法 样品溶解后,采用ICP-MS半定量测定模式对注射用亚锡甲氧异腈中元素杂质进行初步筛查,结合国际人用药品注册技术协调会(International Council for Harmonisation of Technical Requirements for Pharmaceuticals for Human Use,ICH)Q3D元素杂质指导原则的要求,确定16种元素:锂(Li)、镁(Mg)、铝(Al)、硅(Si)、钾(K)、钒(V)、铁(Fe)、钴(Co)、镍(Ni)、锌(Zn)、砷(As)、镉(Cd)、铟(In)、锑(Sb)、汞(Hg)和铅(Pb)作为定量考察和控制的元素杂质研究对象。ICP-MS采集模式选择动能歧视模式进行定量方法研究,分别以钪(Sc)、锗(Ge)、钇(Y)、铋(Bi)作为内标,测定16种元素杂质的含量。结果 16种元素杂质在各自线性范围内响应与浓度相关性良好(r≥0.999 3);方法精密度(RSD≤3.53%)和重复性(RSD≤3.69%)均较好;各元素平均回收率为95.86%~105.64%(RSD≤5.06%,n=9),方法准确性良好。注射用亚锡甲氧异腈样品中16种元素均未超出限度,Mg、K、Zn 3种元素含量相对较高。结论 金属盐类制剂产品可能引入ICH Q3D原则要求以外的元素杂质。本研究建立的ICP-MS定量方法简便、快速,可用于注射用亚锡甲氧异腈中元素杂质的筛查、检测和风险评估。
