The analog signal processor of the Auger fluorescence detector prototype

The Auger Fluorescence Detector will allow to determine the longitudinal development of atmospheric showers in the range 10 19 –10 21 eV. A detector module comprises an array of 20 � 22 PMTs at the focal surface of a large-aperture telescope. Thirty such modules will be used. The PMTs pixel signal is variable in shape depending on the shower-eye geometry. The sky background light (BL) is also variable. We have developed an analog signal processor to obtain best energy and timing resolution despite those constrains. The Head Electronics (HE) bias the PMTs and keeps its pulsegain constant even for large BL. This is measured using a current-monitor of novel design. Both the signal pulse and the BL DC level are sent via a single twisted pair to the Analog Board (AB). The AB performs the compression of the 15–16 bit signal dynamic range into 12 bits of the FADC which follows the AB. A three-pole Bessel filter was adopted for antialiasing. The AB includes 16 bit sigma-delta chips to readout the BL DC level, and a test-pulse distribution system. # 2001 Elsevier Science B.V. All rights reserved. PACS: 29.4

Liquid krypton electromagnetic calorimeter

Abstract A calorimeter using 30 tons of liquid krypton for the KEDR detector is being constructed. The main effects which determine the energy and space resolution have been studied. An energy resolution of 1.7% at 1.2 GeV was obtained with the prototype. A space resolution of 0.4 mm for relativistic particles has been reached with the prototype

Unsubstituted phenothiazine as a superior water-insoluble mediator for oxidases

The mediation of oxidases glucose oxidase (GOx), lactate oxidase (LOx) and cholesterol oxidase (ChOx) by a new electron shuttling mediator, unsubstituted phenothiazine (PTZ), was studied. Cyclic voltammetry and rotating-disk electrode measurements in nonaqueous media were used to determine the diffusion characteristics of the mediator and the kinetics of its reaction with GOx, giving a second-order rate constant of 7.6×103–2.1×104 M−1 s−1 for water–acetonitrile solutions containing 5–15% water. These values are in the range reported for commonly used azine-type mediators, indicating that PTZ is able to function as an efficient mediator. PTZ and GOx, LOx and ChOx were successfully co-immobilised in sol–gel membrane on a screen-printed electrode to construct glucose, lactate and cholesterol biosensors, respectively, which were then optimised in terms of stability and sensitivity. The electrocatalytic oxidation responses showed a dependence on substrate concentration ranging from 0.6 to 32 mM for glucose, from 19 to 565 mM for lactate and from 0.015 to 1.0 mM for cholesterol detection. Oxidation of substrates on the surface of electrodes modified with PTZ and enzyme membrane was investigated with double-step chronoamperometry and the results showed that the PTZ displays excellent electrochemical catalytic activities even when immobilised on the surface of the electrode

Creatinine and urea biosensors based on a novel ammonium ion-selective copper-polyaniline nano-composite

The use of a novel ammonium ion-specific copper-polyaniline nano-composite as transducer for hydrolase-based biosensors is proposed. In this work, a combination of creatinine deaminase and urease has been chosen as a model system to demonstrate the construction of urea and creatinine biosensors to illustrate the principle. Immobilisation of enzymes was shown to be a crucial step in the development of the biosensors; the use of glycerol and lactitol as stabilisers resulted in a significant improvement, especially in the case of the creatinine, of the operational stability of the biosensors (from few hours to at least 3 days). The developed biosensors exhibited high selectivity towards creatinine and urea. The sensitivity was found to be 85±3.4 mA M−1 cm−2 for the creatinine biosensor and 112±3.36 mA M−1 cm−2 for the urea biosensor, with apparent Michaelis–Menten constants (KM,app), obtained from the creatinine and urea calibration curves, of 0.163 mM for creatinine deaminase and 0.139 mM for urease, respectively. The biosensors responded linearly over the concentration range 1–125 µM, with a limit of detection of 0.5 µM and a response time of 15 s. The performance of the biosensors in a real sample matrix, serum, was evaluated and a good correlation with standard spectrophotometric clinical laboratory techniques was found