流动注射在线分离富集-火焰原子吸收光谱法测定环境水样中Cr(Ⅲ)和Cr(Ⅵ)的形态

采用单阀阴离子和阳离子交换树脂微柱并联 ,两柱交替采样逆向洗脱流动注射在线分离富集环境水样中Cr(Ⅲ )和Cr(Ⅵ ) ,分别用 15 %HNO3和 8%NH4 NO3洗脱 ,火焰原子吸收光谱法直接检测。富集 1min时Cr(Ⅲ )和Cr(Ⅵ )的特征浓度分别为 :1 5 0 μg·L- 1 和 1 39μg·L- 1 ,Cr(Ⅲ )和Cr(Ⅵ )检出限 (3σ)分别为 1 0 3μg·L- 1 和 0 5 4 μg·L- 1 ;相对标准偏差 (10 μg·L- 1 )分别为 :3 4 1%和 1 80 % ,分析样品加标回收率在 93 5 %～ 10 7 5 %之间。     

Charged-Lepton-Flavour Violation in the light of the Super-Kamiokande data

Motivated by the data from Super-Kamiokande and elsewhere indicating oscillations of atmospheric and solar neutrinos, we study charged-lepton-flavour violation, in particular the radiative decays and , but also commenting on and decays, as well as conversion on nuclei. We first show how the renormalization group may be used to calculate flavour-violating soft supersymmetry-breaking masses for charged sleptons and sneutrinos in models with universal input parameters. Subsequently, we classify possible patterns of lepton-flavour violation in the context of phenomenological neutrino mass textures that accommodate the Super-Kamiokande data, giving examples based on Abelian flavour symmetries. Then we calculate in these examples rates for and , which may be close to the present experimental upper limits, and show how they may distinguish between the different generic mixing patterns. The rates are promisingly large when the soft supersymmetry-breaking mass parameters are chosen to be consistent with the cosmological relic-density constraints. In addition, we discuss conversion on Titanium, which may also be accessible to future experiments. Received: 18 December 1999 / Published online: 6 March 2000     

Note on Signature Change and Colombeau Theory

Recent work alludes to various 'controversies' associated with signature change in general relativity and claims to resolve them. As we have argued previously, these are in fact disagreements about the (often unstated) assumptions underlying various possible approaches. We demonstrate that the issue has not been resolved and the choice between approaches remains open.     

Binary group and Chinese postman polyhedra

A new proof of the characterization of the Chinese postman polyhedra is given. In developing this proof, a theorem of Gomory about homomorphic lifting of facets for group polyhedra is generalized to subproblems. Some results for the Chinese postman problem are generalized to binary group problems. In addition, a connection is made between Fulkerson's blocking polyhedra and a blocking pair of binary group problems. A connection is also developed between minors and lifting of facets for group problems.     

Fragmentation pathways of 2,3‐dimethyl‐2,3‐dinitrobutane cations in the gas phase

2,3‐Dimethyl‐2,3‐dinitrobutane (DMNB) is an explosive taggant added to plastic explosives during manufacture making them more susceptible to vapour‐phase detection systems. In this study, the formation and detection of gas‐phase [M+H]⁺, [M+Li]⁺, [M+NH₄]⁺ and [M+Na]⁺ adducts of DMNB was achieved using electrospray ionisation on a triple quadrupole mass spectrometer. The [M+H]⁺ ion abundance was found to have a strong dependence on ion source temperature, decreasing markedly at source temperatures above 50°C. In contrast, the [M+Na]⁺ ion demonstrated increasing ion abundance at source temperatures up to 105°C. The relative susceptibility of DMNB adduct ions toward dissociation was investigated by collision‐induced dissociation. Probable structures of product ions and mechanisms for unimolecular dissociation have been inferred based on fragmentation patterns from tandem mass (MS/MS) spectra of source‐formed ions of normal and isotopically labelled DMNB, and quantum chemical calculations. Both thermal and collisional activation studies suggest that the [M+Na]⁺ adduct ions are significantly more stable toward dissociation than their protonated analogues and, as a consequence, the former provide attractive targets for detection by contemporary rapid screening methods such as desorption electrospray ionisation mass spectrometry. Copyright © 2009 Commonwealth of Australia. Published by John Wiley & Sons, Ltd.