Collectivity and configuration mixing in 186,188Pb and 194Po

Lifetimes of prolate intruder states in 186Pb and oblate intruder states in 194Po have been determined by employing, for the first time, the recoil-decay tagging technique in recoil distance Doppler-shift lifetime measurements. In addition, lifetime measurements of prolate states in 188Pb up to the 8+ state were carried out using the recoil-gating method. The B(E2) values have been deduced from which deformation parameters |beta2|=0.29(5) and |beta2|=0.17(3) for the prolate and the oblate bands, respectively, have been extracted. The results also shed new light on the mixing between different shapes.     

Observation of Runaway Electron Behaviour During Disruptions in LHCD Discharges in the HT‐7 Tokamak

Production of runaway electrons during disruptions has been observed in the HT‐7 Tokamak. The runaway current plateaus, which can carry part of the pre‐disruptive current, are observed in lower‐hybrid current drive (LHCD) limiter discharges. It is found that the runaway current can mitigate the disruptions effectively. We can use gas puffing to increase the line‐averaged density to restrain the runaway electrons and rebuild the plasmas after the disruptions. Detailed observations are presented on the runaway electrons generated following disruptions in the HT‐7 tokamak discharges. The results indicate that the magnetic oscillations play a significant role in the loss of runaway electrons in disruptions. There are two important preconditions to rebuild plasmas by runaway electrons after the disruptions. One of them are weak magnetic oscillations; another one are LHWs (lower‐hybrid waves) (© 2011 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim)     

Separation of Dietary Folates by Gradient Reversed-Phase HPLC: Comparison of Alternative and Conventional Silica-Based Stationary Phases

A study of ten silica-based stationary phases and gradient elution conditions to separate dietary folates by reversed-phase HPLC was performed. Alkyl-bonded stationary phases (both conventional and alternative) were found to be the most promising for the separation of different folate monoglutamates in terms of selectivity and peak shape. These phases were better than phenyl-bonded phases which lacked selectivity when separating 10-formyl-folic acid and 5-formyl-tetrahydrofolate. Polar-bonded (cyano) stationary phase showed similar retention characteristics as the conventional alkyl-bonded phases, but ranked below those in terms of peak shape. Overall, alternative stationary phases exhibited slightly higher retention of late-eluted folates and greater retention variability for early-eluting tetrahydrofolate and 5-methyl-tetrahydrofolate. Best selectivity was achieved on alternative polar endcapped Aquasil C₁₈ followed by conventional Synergy MAX C₁₂ and Genesis C₁₈ stationary phases.     

Biodistribution and bioactivity of tetra-pegylated meta-tetra(hydroxyphenyl)chlorin compared to native meta-tetra(hydroxyphenyl)chlorin in a rat liver tumor model

It has been proposed that the construction of a photosensitizer-polymer conjugate would lead to an increased selective retention of the drug in tumor tissue resulting in an enhancement of selective tumor destruction by light in photodynamic therapy. In this study the kinetics of a tetra-pegylated derivative of meta-tetra(hydroxyphenyl)chlorin (mTHPC-PEG) were compared with those of native meta-tetra(hydroxyphenyl)chlorin (mTHPC) in a rat liver tumor model. In addition, the time course of bioactivity of both drugs was studied in normal liver tissue. Pegylation of mTHPC resulted in a two-fold increase in the plasma half-life time, a five-fold decrease in liver uptake and an increase in the tumor selectivity at early time intervals after drug administration. However, although mTHPC concentrations in liver decrease rapidly with time, mTHPC-PEG liver concentrations increased as a function of time. This led to a loss of tumor selectivity at all but the earliest time points, whereas with mTHPC tumor selectivity increased with time. For both drugs the time course of bioactivity in the liver parallels drug concentration levels with extensive necrosis after irradiation of mTHPC-PEG-sensitized liver tissue up to drug-light intervals of 120 h. It is concluded that on balance mTHPC-PEG does not appear to show any benefits over native mTHPC for the treatment of liver tumors, as normal liver tissue accumulates the compound. However, pegylation is a potentially promising strategy with an increase in tumor selectivity and reduced liver uptake if accumulation in the liver can be prevented.     

In-beam gamma-ray spectroscopy of 190, 197Po

γ -ray transitions in the neutron-deficient nuclei ^{190, 197}Po have been identified using the JUROGAM Ge detector array coupled to the RITU gas-filled separator and the GREAT spectrometer. The yrast band of ¹⁹⁰Po has been firmly established through γ -γ coincidences and extended up to a spin and parity of 14⁺. It displays similar behaviour to its isotones ¹⁸⁶Hg and ¹⁸⁸Pb above the 4⁺ level, thus confirming its prolate nature. In ¹⁹⁷Po the band built upon the 13/2⁺ isomer has been extended up to a spin and parity of 33/2⁺, while the non-yrast band has been observed for the first time. The behaviour of ¹⁹⁷Po is found to be similar to that of the nearby even-mass isotopes, which is consistent with the model in which the i _13/2 neutron is weakly coupled to the states in the even-even core.     

Collectivity in neutron-deficient Pb and Po nuclei

Lifetimes of low-lying yrast states in ¹⁸⁶Pb and ¹⁹⁴Po have been determined by employing, for the first time, the recoil-decay tagging technique in recoil distance Doppler-shift lifetime measurements. In addition, lifetime measurements of prolate states in ¹⁸⁸Pb up to the 8⁺ state were carried out using the recoil gating method. The deformation parameters and for the prolate (^186,188Pb) and the oblate (¹⁹⁴Po) bands, respectively, have been extracted from the measured lifetimes. 27.70.+q–