High purity magnesium is not only an important basic raw material for semiconductor and electronics industries,but also a promising new generation of electrochemical energy storage materials and biomedical materials.I...High purity magnesium is not only an important basic raw material for semiconductor and electronics industries,but also a promising new generation of electrochemical energy storage materials and biomedical materials.Impurities in high-purity magnesium affect material properties,which has become the most critical factor restricting its application.However,accurate analysis of multiple ultra-trace impurity elements in high-purity magnesium is extremely challenging.In this paper,based on the synergistic effect of N_(2)O/H_(2) reaction gas mixture to eliminate spectral interference of inductively coupled plasma tandem mass spectrometry(ICP-MS/MS),a new strategy for the quantification of 45 ultra-trace impurity elements in high-purity magnesium was proposed.The results indicated that the limits of detection(LOD)were in the range of 0.02–18.5 ng L^(−1);the LODs of the challenging non-metallic elements Si and S were 18.5 and 12.2 ng L^(−1),respectively;and the LODs of all the other analytes were less than 10 ng L^(−1).Even under hot plasma conditions,LODs of alkali metal elements were also less than 5 ng L^(−1).The spike recovery of each analyte was 93.6%–107%,and the relative standard deviation(RSD)was 3.2%–6.9%,respectively.At a 95%level of confidence,no significant differences were found between the results obtained under the optimal conditions for the analyte with the developed method and the measurement results of SF-ICP-MS.The developed method indicated low LOD,high sample throughput,and complete interference elimination,demonstrating a new avenue for the rapid determination of ultra-trace elements in high-purity magnesium.展开更多
In this paper,two numerical schemes for the multi-term fractional mixed diffusion and diffusion-wave equation(of order a,with 0<a<2)are developed to solve the initial value problem.Firstly,we study a direct nume...In this paper,two numerical schemes for the multi-term fractional mixed diffusion and diffusion-wave equation(of order a,with 0<a<2)are developed to solve the initial value problem.Firstly,we study a direct numerical scheme that uses quadratic Charles Hermite and Newton(H2N2)interpolation polynomials approximations in the temporal direction and finite element discretization in the spatial direction.We prove the stability of the direct numerical scheme by the energy method and obtain a priori error estimate of the scheme with an accuracy of order 3a.In order to improve computational efficiency,a new fast numerical scheme based on H2N2 interpolation and an efficient sum-of-exponentials approximation for the kernels is proposed.Numerical examples confirm the error estimation results and the validity of the fast scheme.展开更多
The novel copper?complex with salicylaldehyde benzoylhydrazone and pyridine ligands, Cu(C14H10N2O2)(C5H5N), has been synthesized and characterized by elemental analysis, IR and thermal analysis. The crystal structure ...The novel copper?complex with salicylaldehyde benzoylhydrazone and pyridine ligands, Cu(C14H10N2O2)(C5H5N), has been synthesized and characterized by elemental analysis, IR and thermal analysis. The crystal structure of the title complex has been determined by single crystal X ray diffraction techniques. The crystal belongs to monoclinic with space group P21/c. The cell parameters are: a=1.6362(9)nm, b=1.7140(9)nm, c=1.2255(7)nm, β=105.168(9)°, V=3.317(3)nm3, Z=8, Dc=1.525g·cm-3, μ(MoKα)=1.334mm-1, F(000)=1560. The structure wasrefined to final R1=0.0376, wR2=0.0909. The copper?ion lies in a distorted square planar environment composed of two oxygen atoms, one nitrogen atom of tridentate acyhydrazone Schiff base ligand and one nitrogen atom of the pyridine ligand. CCDC: 193111.展开更多
A new zinc hydrogen phosphite C4H8N2H4·Zn（HPO3）2 was prepared by hydrothermal method in the presence of piperazine as a structure-directing agent and the crystal structure was determined by single-crystal X-ray...A new zinc hydrogen phosphite C4H8N2H4·Zn（HPO3）2 was prepared by hydrothermal method in the presence of piperazine as a structure-directing agent and the crystal structure was determined by single-crystal X-ray diffraction analysis and further characterized by X-ray powder diffraction, IR, ICP, elemental analysis and TG analysis. This compound has one-dimensional anionic chains containing four-membered rings built from corner-sharing linked alternating ZnO4 tetrahedra and HPO3 pseudo pyramids. The zinc hydrogen phosphite chains are interacted with the templates of diprotonated piperazine by N—H…O hydrogen bond. Crystal data for C4H8N2H4·Zn（HPO3）2∶monoclinic, space group C2/c. a=1.774 8（2） nm, b=0.724 28（9） nm, c=0.880 87（11） nm, β= 105.345（3）°, V=1.091 9（2） nm 3, Z=4, Dc=1^907 Mg/m 3, R1=0.022 9, wR2=0.058 8.展开更多
基金supported by the Natural Science Foundation of China(52171103 and 21975289).
文摘High purity magnesium is not only an important basic raw material for semiconductor and electronics industries,but also a promising new generation of electrochemical energy storage materials and biomedical materials.Impurities in high-purity magnesium affect material properties,which has become the most critical factor restricting its application.However,accurate analysis of multiple ultra-trace impurity elements in high-purity magnesium is extremely challenging.In this paper,based on the synergistic effect of N_(2)O/H_(2) reaction gas mixture to eliminate spectral interference of inductively coupled plasma tandem mass spectrometry(ICP-MS/MS),a new strategy for the quantification of 45 ultra-trace impurity elements in high-purity magnesium was proposed.The results indicated that the limits of detection(LOD)were in the range of 0.02–18.5 ng L^(−1);the LODs of the challenging non-metallic elements Si and S were 18.5 and 12.2 ng L^(−1),respectively;and the LODs of all the other analytes were less than 10 ng L^(−1).Even under hot plasma conditions,LODs of alkali metal elements were also less than 5 ng L^(−1).The spike recovery of each analyte was 93.6%–107%,and the relative standard deviation(RSD)was 3.2%–6.9%,respectively.At a 95%level of confidence,no significant differences were found between the results obtained under the optimal conditions for the analyte with the developed method and the measurement results of SF-ICP-MS.The developed method indicated low LOD,high sample throughput,and complete interference elimination,demonstrating a new avenue for the rapid determination of ultra-trace elements in high-purity magnesium.
基金supported by the State Key Program of the National Natural Science Foundation of China(No.11931003)by the Grants(Nos.41974133 and 12271233).
文摘In this paper,two numerical schemes for the multi-term fractional mixed diffusion and diffusion-wave equation(of order a,with 0<a<2)are developed to solve the initial value problem.Firstly,we study a direct numerical scheme that uses quadratic Charles Hermite and Newton(H2N2)interpolation polynomials approximations in the temporal direction and finite element discretization in the spatial direction.We prove the stability of the direct numerical scheme by the energy method and obtain a priori error estimate of the scheme with an accuracy of order 3a.In order to improve computational efficiency,a new fast numerical scheme based on H2N2 interpolation and an efficient sum-of-exponentials approximation for the kernels is proposed.Numerical examples confirm the error estimation results and the validity of the fast scheme.
文摘The novel copper?complex with salicylaldehyde benzoylhydrazone and pyridine ligands, Cu(C14H10N2O2)(C5H5N), has been synthesized and characterized by elemental analysis, IR and thermal analysis. The crystal structure of the title complex has been determined by single crystal X ray diffraction techniques. The crystal belongs to monoclinic with space group P21/c. The cell parameters are: a=1.6362(9)nm, b=1.7140(9)nm, c=1.2255(7)nm, β=105.168(9)°, V=3.317(3)nm3, Z=8, Dc=1.525g·cm-3, μ(MoKα)=1.334mm-1, F(000)=1560. The structure wasrefined to final R1=0.0376, wR2=0.0909. The copper?ion lies in a distorted square planar environment composed of two oxygen atoms, one nitrogen atom of tridentate acyhydrazone Schiff base ligand and one nitrogen atom of the pyridine ligand. CCDC: 193111.
文摘A new zinc hydrogen phosphite C4H8N2H4·Zn（HPO3）2 was prepared by hydrothermal method in the presence of piperazine as a structure-directing agent and the crystal structure was determined by single-crystal X-ray diffraction analysis and further characterized by X-ray powder diffraction, IR, ICP, elemental analysis and TG analysis. This compound has one-dimensional anionic chains containing four-membered rings built from corner-sharing linked alternating ZnO4 tetrahedra and HPO3 pseudo pyramids. The zinc hydrogen phosphite chains are interacted with the templates of diprotonated piperazine by N—H…O hydrogen bond. Crystal data for C4H8N2H4·Zn（HPO3）2∶monoclinic, space group C2/c. a=1.774 8（2） nm, b=0.724 28（9） nm, c=0.880 87（11） nm, β= 105.345（3）°, V=1.091 9（2） nm 3, Z=4, Dc=1^907 Mg/m 3, R1=0.022 9, wR2=0.058 8.
