Re-evaluation of correction factors of a primary standard graphite calorimeter in 60Co gamma ray beams as a basis for the appointment of the BEV absorbed dose rate to water reference value

The graphite calorimeter of the Federal Office of Metrology and Surveying (BEV-Bundesamt für Eich- und Vermessungswesen) was established in the 1980s as the primary standard for the absorbed dose to water for (60)Co gamma ray beams. To maintain the primary standard at an international level the graphite calorimeter and its corresponding components had to undergo a refurbishment and modernisation process. The correction factors of the graphite calorimeter were re-evaluated with Monte Carlo and experimental methods to obtain improved values. These are the correction for the effect of the gaps (1.0061), the scaling correction (0.9998), the correction for the difference in air attenuation (0.9971) and the corrections for the effective measurement depths in the graphite phantom for the graphite calorimeter (0.9886) and the CC01-105 ionisation chamber (0.9913). Consequently, it was necessary to change the reference value for the absorbed dose rate to water of the (60)Co teletherapy unit used for the calibration of secondary standard dosemeters.     

Determination of Caffeine,Myosmine, and Nicotine in Chocolate by Headspace Solid‑Phase Microextraction Coupled with Gas Chromatography‑Tandem Mass Spectrometry

The occurrence of the bioactive components caffeine (xanthine alkaloid), myosmine and nicotine (pyridine alkaloids) in different edibles and plants is well known, but the content of myosmine and nicotine is still ambiguous in milk/dark chocolate. Therefore, a sensitive method for determination of these components was established, a simple separation of the dissolved analytes from the matrix, followed by headspace solid?phase microextraction coupled with gas chromatography‐tandem mass spectrometry (HS?SPME?GC?MS/MS). This is the first approach for simultaneous determination of caffeine, myosmine, and nicotine with a convenient SPME technique. Calibration curves were linear for the xanthine alkaloid (250 to 3000 mg/kg) and the pyridine alkaloids (0.000125 to 0.003000 mg/kg). Residuals of the calibration curves were lower than 15%, hence the limits of detection were set as the lowest points of the calibration curves. The limits of detection calculated from linearity data were for caffeine 216 mg/kg, for myosmine 0.000110 mg/kg, and for nicotine 0.000120 mg/kg. Thirty samples of 5 chocolate brands with varying cocoa contents (30% to 99%) were analyzed in triplicate. Caffeine and nicotine were detected in all samples of chocolate, whereas myosmine was not present in any sample. The caffeine content ranged from 420 to 2780 mg/kg (relative standard deviation 0.1 to 11.5%) and nicotine from 0.000230 to 0.001590 mg/kg (RSD 2.0 to 22.1%).     

Unifying Energetic Disorder from Charge Transport and Band Bending in Organic Semiconductors

Characterizing the density of states (DOS) width accurately is critical in understanding the charge‐transport properties of organic semiconducting materials as broader DOS distributions lead to an inferior transport. From a morphological standpoint, the relative densities of ordered and disordered regions are known to affect charge‐transport properties in films; however, a comparison between molecular structures showing quantifiable ordered and disordered regions at an atomic level and its impact on DOS widths and charge‐transport properties has yet to be made. In this work, for the first time, the DOS distribution widths of two model conjugated polymer systems are characterized using three different techniques. A quantitative correlation between energetic disorder from band‐bending measurements and charge transport is established, providing direct experimental evidence that charge‐carrier mobility in disordered materials is compromised due to the relaxation of carriers into the tail states of the DOS. Distinction and quantification of ordered and disordered regions of thin films at an atomic level is achieved using solid‐state NMR spectroscopy. An ability to compare solid‐state film morphologies of organic semiconducting polymers to energetic disorder, and in turn charge transport, can provide useful guidelines for applications of organic conjugated polymers in pertinent devices.