New precise determination of the \tau lepton mass at KEDR detector

The status of the experiment on the precise $\tau$ lepton mass measurement running at the VEPP-4M collider with the KEDR detector is reported. The mass value is evaluated from the $\tau^+\tau^-$ cross section behaviour around the production threshold. The preliminary result based on 6.7 pb$^{-1}$ of data is $m_{\tau}=1776.80^{+0.25}_{-0.23} \pm 0.15$ MeV. Using 0.8 pb$^{-1}$ of data collected at the $\psi'$ peak the preliminary result is also obtained: $\Gamma_{ee}B_{\tau\tau}(\psi') = 7.2 \pm 2.1$ eV.Comment: 6 pages, 8 figures; The 9th International Workshop on Tau-Lepton Physics, Tau0

Design of quinonoid-enriched humic materials with enhanced rediox properties.

The primary goal of this work was to develop quinonoid-enriched humic materials with enhanced redox properties that could be used as potentially effective redox mediators and reducing agents for in situ remediation of soil and aquatic environments. Two different strategies were formulated and tested to derive these materials. The first strategy called for the oxidation of phenolic fragments associated with the humic aromatic core. In a second strategy, polycondensation of these phenolic fragments was carried out with hydroquinone and catechol. The oxidized derivatives and copolymers obtained were characterized using elemental and functional group analyses, and capillary zone electrophoresis. The redox properties were evaluated using ESR spectrometry and reducing capacity determinations. The reducing capacities of copolymers ranged between 1 and 4 mmol/g, which were much higher than the parent material and the oxidized derivatives. Hence, preference should be given to the copolycondensation approach. The quinonoid-enriched humics are nontoxic, water soluble, and resistant to biodegradation; thus, they could be applied as soil amendments to reduce highly mobile oxoanions of heavy metals and radionuclides, or as redox mediators to enhance in situ bioremediation. Otherwise, cross-linked copolymers could be created to serve as inexpensive reductants in permeable reactive barriers designed to remove highly oxidized contaminants from polluted groundwaters

Quantitative and qualitative precision improvements by effective mobility-scale data transformation in capillary electrophoresis analysis.

By transforming the time-based x-axis of electropherograms in capillary zone electrophoresis (CZE) into the corresponding effective mobility-scale, we propose a simple and robust data representation for a better qualitative and quantitative capillary electrophoresis (CE) analysis. The time scale of the raw electrophoretic data (detection signal versus time) is transformed into an effective electrophoretic mobility scale (mu eff-scale) with account of the electroosmotic flow (EOF) peak or of an internal standard of known effective mobility. With the new scaling (detection signals versus effective mobility), the obtained electropherograms are more representative of the velocity-based electrophoretic separation and the comparison of complete electropherograms is directly possible. This is of importance when tracking peaks in real samples where alteration in EOF stability can occur or when comparing electrophoretic runs from different experimental setups (independence in column length and voltage). Beside the qualitative possibilities, a quantitative improvement is achieved in the mu eff-scale with significant better peak area reproducibility and equal to more precision in quantitative analysis than with the primary time-scale integration