Proton tracks and the formation of pores in poly[diethylene glycol bis-(allyl carbonate)].

Modern dosimetry needs efficient detectors for registering light ions, especially light ions having energies of up to 10 MeV/amu. That is why this research pays attention to the development of materials for such a task. In this work, a CR-39 detector, which is the most efficient detector, was used. It was irradiated with low-energy protons. Using sensitive electrolytic etching and electron scanning microscopy, a complete analysis was carried out of the process of the formation of a pore starting from its opening to the final stage of its formation. The process of sequential track breakthroughs was observed. The data obtained on the shape of the pore and the parameters of its formation allow simulation of the process of etching. The etch rates and sensitivity of etching are determined. The influence of energy losses on the geometry of the pore is considered.

Experience in long-term neutron dose equivalent measurements using etched track detectors with (n,alpha) converters in moderators.

Etched track Makrofol detectors combined with Kodak BN-1 boron (n,alpha) converters were used inside a 30 cm diameter polyethylene (PE) sphere for the measurement of the neutron ambient dose equivalent. We found unexpectedly high values for the neutron dose equivalent of about 250 microSv instead of 25 microSv for 3 months' exposure in the natural environment. Results from such detectors etched in the authors' labortories revealed that the tracks could only be induced by spontaneous particle emission from the converter. This was confirmed by track diameter analysis and additional special etching of deeper detector layers. Eight surface barrier detectors were used simultaneosly for several days to measure the alpha spectra of the converters. The overall count rate in the energy range 2.5-7.5 MeV was 10 alpha particles d(-1) x cm(-2) for most of the converters and about 10 times less than this for some of them. To identify the nuclides responsible for alpha emission within the converters, gamma spectra of converters were measured for 8 days using a highly sensitive low-background gamma spectrometry system The spectra clearly indicated a small contamination (10 +/- 3 mBq) of the converter foils with 225Ra (T(1/2) = 5.7 y) typically originating from 232Th.

Quantitative thin-layer chromatographic determination of dihydroergot alkaloids.

Direct, quantitative, thin-layer chromatographic methods for the determination of dihydroergot alkaloids are described, in particular the determination of dihydroergotamine with dihydroergokryptine as internal standard. The internal standard was added to plasma, which was extracted twice in dichloromethane; the organic phase was removed under nitrogen, the residue resolved in ethanol and applied on a silica gel G-60 plate. Dihydroergotamine and the internal standard can be measured directly by fluorescence, with excitation at 264 nm and with use of a Zeiss remission filter FL 39. The percentage recovery from this method is 49.17 +/- 6.71% (plasma). These methods enable the determination of 10 pmol dihydroergotamine per ml of plasma (ca. 6.8 ng/ml) with a coefficient of variation of 10.3%. They have proved useful in biochemical and pharmaceutical applications.