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61.
62.
电化学氢化物发生-原子荧光法测定环境样品中的Se(Ⅳ)和Se(Ⅵ) 总被引:1,自引:0,他引:1
设计了一种新的电化学氢化物发生装置, 用于测定不同价态的硒. 通过对传统的平板电解池的改进, 设计了全新的圆盘电解池并采用螺纹密封的方式, 极大地缩短了电解池的装配时间, 提高了电解池的使用寿命和密封性能. 结合热水浴在线还原技术, 将 Se(Ⅵ)在高浓度HCl介质中120 s内还原成Se(Ⅳ), 通过电化学氢化物发生技术生成氢化物, 成功的进行硒的在线价态分析. 对各种实验参数进行了详细的研究, Se(Ⅳ) 和Se(Ⅵ)的相对标准偏差分别为2.6% 和 3.1% (n=11);Se(Ⅳ)和总硒的检出限分别为0.32和0.27 μg/L (3σ). 相似文献
63.
电热原子吸收法测定人发中硒时不同改进剂的研究 总被引:2,自引:0,他引:2
对于生物体中硒的测定,国内外已有大量报道,所用方法也相当广泛。本文利用石墨炉原子吸收对人发中硒的测定进行了研究;对使用较多的两种硒的基体改进剂:铜与镍的作用与效果进行了研究,发现铜较镍在某些方面更为优越。当选用100 μg/mL的铜作改进剂时,硒的特征浓度为0.13 ng/1%abs,测定精度为3.4%~5.4%;线性范围达400 ng。 相似文献
64.
本文对如何从单一二维交换谱提取速率常数进行了理论分析,提出了一种近似处理方法,即把较短混合时间τ_m内在二维平面上磁化强度传递看成是单向进行的,进而导出了二维交换谱中所有峰强随τ_m变化的表达式。所得结果与Ernst的精确结果在一级近似下完全一致,在二级近似下略有不同,但将难以求解的问题转化成简单的代数方程、用这一方法对新近获得的SnCl_4·5H_2O在水溶液中的~(119)Sn二维交换谱进行了处理,得到与实验相吻合的结果,并求得了SnCI_6~(2-)水解体系的动态交换速率常数。 相似文献
65.
Werner Paschinger Kunio Yubuta Yuta Saiga Toshiro Takabatake Gerald Giester Peter Rogl 《ChemInform》2016,47(29):no-no
Single crystals of Ce3Pt4Sn6 (I) and Ce1‐xPt6Al13+2x (x = 0.207, (II)) are isolated by mechanical fragmentation of specimens grown from self‐fluxes (Sn or Al, resp.) by slow cooling from the melt. 相似文献
66.
Shabbir Hussain Saira Shahzadi Muhammad Shahid Asif Ali Tahir Syed Mustansar Abbas 《Journal of Coordination Chemistry》2017,70(24):4070-4092
Bimetallic chlorodi-/triorganotin(IV) derivatives of general formulas R2(H2O)SnLCSSSn(Cl)R2 (R=Me: 1; Ph: 2) and R3Sn(Na)LCSSSnR3·H2O (R=Bu: 3; Ph: 4) were prepared by reaction of iminodiacetic acid disodium salt hydrate (Na2LH) with CS2 and R2SnCl2/R3SnCl in methanol. The reaction between Na2LH, CS2, and PdCl2 produced [Na2LCSS]2Pd·2H2O (5) which was treated with R3SnCl to synthesize the heterobimetallic derivatives [R3Sn(Na)LCSS]2Pd·2H2O (R=Me: 6; Ph: 7). The complexes were characterized by microanalysis, spectroscopic, and thermogravimetric analyses. Elemental analysis data, mass fragmentation, and thermal degradation patterns supported the molecular composition of the complexes. FT-IR data indicated monodentate binding of carboxylate while a chelating coordination mode of the dithiocarboxylate was verified in the solid state. A five-coordinate tin(IV) was demonstrated in the solid state. In solution, a tetrahedral/trigonal bipyramidal configuration around Sn(IV) and a square planar geometry of Pd(II) was indicated by multinuclear NMR (1H and 13C) and UV-visible studies. The Pd(II) derivatives showed interaction with salmon sperm-DNA and caused an inhibition of alkaline phosphatase (ALPs). The antibacterial/antifungal potential of the coordination products varied with the nature of incorporated metal and a substitution pattern at tin(IV); the palladium metallation decreased the antimicrobial activities. The triorganotin(IV) products exhibited more powerful action against bacteria/fungi as compared to their diorganotin(IV) counterparts. The complexes displayed sufficiently lower hemolytic effects in vitro as compared to triton X-100 and slightly higher than PBS. 相似文献
67.
We report the first use of functionalized Ag2Se nanoparticles (NPs) as effective extracting probes for NPs-based liquid-phase microextraction (NPs-LPME) to analyze hydrophobic peptides and proteins from biological samples (urine and plasma) and soybean in matrix-assisted laser desorption/ionization mass spectrometry (MALDI-MS). Surface modified functional groups such as octadecanethiol (ODT) and 11-mercaptoundecanoic acid (MUA) on Ag2Se NPs were found to play an important role for efficient extraction of peptides and proteins from test samples through hydrophobic interactions. The peptides can be efficiently extracted using functionalized Ag2Se NPs as extracting probes in the presence of high concentration of matrix interferences such as 4 M urea, 0.5% Triton X-100 and 3% NaCl. Ag2Se@ODT NPs have shown better extraction efficiency and detection sensitivity for peptides than Ag2Se@MUA NPs, bare Ag2Se NPs and conventional MALDI-MS. The LODs are 20-68 nM for valinomycin and 100-180 nM for gramicidin D using Ag2Se@ODT NPs-LPME in the MALDI-MS. The current approach is highly sensitive and the target analytes can be effectively isolated without sample loss and efficiently analyzed in MALDI-MS. 相似文献
68.
Donato Ercole Conte Abdelmaula Aboulaich Josette Olivier-Fourcade Christian Jordy 《Journal of solid state chemistry》2010,183(1):65-6650
A comparative study of two Sn-based composite materials as negative electrode for Li-ion accumulators is presented. The former SnB0.6P0.4O2.9 obtained by in-situ dispersion of SnO in an oxide matrix is shown to be an amorphous tin composite oxide (ATCO). The latter Sn0.72[BPO4]0.28 obtained by ex-situ dispersion of Sn in a borophosphate matrix consists of Sn particles embedded in a crystalline BPO4 matrix. The electrochemical responses of ATCO and Sn0.72[BPO4]0.28 composite in galvanostatic mode show reversible capacities of about 450 and 530 mAh g−1, respectively, with different irreversible capacities (60% and 29%). Analysis of these composite materials by 119Sn Mössbauer spectroscopy in transmission (TMS) and emission (CEMS) modes confirms that ATCO is an amorphous SnII composite oxide and shows that in the case of Sn0.72[BPO4]0.28, the surface of the tin clusters is mainly formed by SnII in an amorphous interface whereas the bulk of the clusters is mainly formed by Sn0. The determination of the recoilless free fractions f (Lamb-Mössbauer factors) leads to the effective fraction of both Sn0 and SnII species in such composites. The influence of chemical composition and especially of the surface-to-bulk tin species ratio on the electrochemical behaviour has been analysed for several Snx[BPO4]1−x composite materials (0.17<x<0.91). The cell using the compound Sn0.72[BPO4]0.28 as active material exhibits interesting electrochemical performances (reversible capacity of 500 mAh g−1 at C/5 rate). 相似文献
69.
Hemilability and nonrigidity in a series of mixed P^PE donor ligands where E = O, S, or Se have been studied in palladium and platinum complexes of the type [M{κ2-(dimethylamino)ethylnaphthyl-C,N)}(P^PE)][SbF6] where P^PE = Ph2PCH2P(E)Ph2.The role of the donor in hemilability, regioselectivity and the binding preferences of particular donors trans to the metallated carbon atom were also investigated. NMR parameters including couplings to 195Pt and 77Se were investigated for cis and trans isomers. The magnitude of 2J13C-77Se couplings can readily distinguish the cis and trans isomers. A large through-space 13C-77Se 3J coupling was observed in one of the amino methyl groups of the dppm(Se) complexes. 相似文献
70.
R. M. Shalaby 《Crystal Research and Technology》2010,45(4):427-432
The Sn‐Zn alloys have been considered as lead‐free solders. In this paper, the effect of 0.0, 0.5, 1.0, 1.5 and 2.0 wt.% Indium as ternary additions on melting temperature, structure, microhardness and micro‐creep of the Sn‐9Zn lead‐free solders were investigated. It is shown that the alloying additions of Indium to the Sn‐Zn binary system result in a suppression of the melting point to 187.9 °C. From x‐ray diffraction analysis, a new intermetallic compound phase, designated β‐In3Sn is detected. The formation of an intermetallic compound phase causes a pronounced increase in the electrical resistivity and mechanical strength. Also, an interesting connection between dynamic Young's modulus and the axial ratio (c/a) of the unit cell of the β‐Sn was found in which Young's modulus increases with increasing the axial ratio (c/a). The ternary Sn‐9Zn‐xIn exhibits creep resistance superior to Sn‐9Zn binary alloy. The better creep resistance of the ternary alloy is attributed to solid solution effect and precipitation of In3Sn in the Sn matrix. The addition of small amounts of In is found to refine the effective grain size and consequently, improves hardness. The 89%Sn‐9%Zn‐2%In alloy is a lead‐free solder designed for possible drop‐in replacement of Pb‐Sn solders. (© 2010 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim) 相似文献