Evaluation of etching correction factor for LR115 cellulose nitrate films from track parameters

LR115 cellulose nitrate films efficiency is strongly dependent on the conditions of etching. In this paper a new method to evaluate a correction factor for this effect is given. The film is scanned with an high-resolution scanner, the diameter of the tracks is measured, and the correction factor is calculated from the average diameter of the tracks. The sensitivity of the film is found to have a linear dependence on the average diameter, and the classical correction, based on the residual thickness, can be substituted by a method based on average track diameter.     

Uncertainties evaluation for electrets based devices used in radon detection

In recent years uncertainty evaluation in measurements has achievedgreat importance. National and international standards offerguidelines to evaluate uncertainties, but these procedures are,until now, not well understood by the operators. This is becauseof the fact that a detailed uncertainty evaluation is not aneasy operation and a standard rule to apply in all cases isnot available. Every measurement procedure has its own uncertaintyevaluation. In this work, attention is focused upon the electretion chambers (EIC), widely used in radon concentration measurements.Measurements of gamma radiation sensitivity are performed ina secondary standard calibration laboratory and measurementof radon concentration sensitivity is performed in a radon chamber0.8 m³ in volume. Raw data are analysed to evaluate the calibrationfactors and the combined uncertainties are determined. The aimof the work is to give a practical method to assess the uncertaintyof a radon measurement.     

Transportable automated ammonia sensor based on a pulsed thermoelectrically cooled quantum-cascade distributed feedback laser

A compact ammonia sensor based on a 10-microm single-frequency, thermoelectrically cooled, pulsed quantum-cascade laser with an embedded distributed feedback structure has been developed. To measure NH3 concentrations, we scanned the laser over two absorption lines of its fundamental v2 band. A sensitivity of better than 0.3 parts per million was achieved with just a 1-m optical path length. The sensor is computer controlled and automated to monitor NH3 concentrations continuously for extended periods of time and to store data in the computer memory.     

Variations of the isotopic ratios of uranium in environmental samples containing traces of depleted uranium: theoretical and experimental aspects

The possibility of using conventional analysis, such as gamma spectrometry and alpha spectrometry, for the detection of traces of depleted uranium (DU) in environmental samples has been investigated. The expected values have been compared with the experimental results obtained by using mollusc samples gathered in the Adriatic Sea. The analysis has shown that it is possible to detect DU. if the percentage composition is about 20% depleted uranium and 80% natural uranium, for a sample containing 10 Bq x kg(-1) of 238U. The possibility of extending this approach to samples with any given uranium concentration is investigated.     

Solution structure and stability of tryptophan-containing nucleopeptide duplexes

Covalently linked peptide-oligonucleotide hybrids were used as models for studying tryptophan-DNA interactions. The structure and stability of several hybrids in which peptides and oligonucleotides are linked through a phosphodiester bond between the hydroxy group of a homoserine (Hse) side chain and the 3'-end of the oligonucleotide, have been studied by both NMR and CD spectroscopy and by restrained molecular dynamics methods. The three-dimensional solution structure of the complex between Ac-Lys-Trp-Lys-Hse(p3'dGCATCG)-Ala-OH (p=phosphate, Ac=acetyl) and its complementary strand 5'dCGTAGC has been determined from a set of 276 experimental NOE distances and 33 dihedral angle constraints. The oligonucleotide structure is a well-defined duplex that belongs to the B-form family of DNA structures. The covalently linked peptide adopts a folded structure in which the tryptophan side chain stacks against the 3'-terminal guanine moiety, which forms a cap at the end of the duplex. This stacking interaction, which resembles other tryptophan-nucleobase interactions observed in some protein-DNA complexes, is not observed in the single-stranded form of Ac-Lys-Trp-Lys-Hse(p3'dGCATCG)-Ala-OH, where the peptide chain is completely disordered. A comparison with the pure DNA duplex, d(5'GCTACG3')-(5'CGTAGC3'), indicates that the interaction between the peptide and the DNA contributes to the stability of the nucleopeptide duplex. The different contributions that stabilize this complex have been evaluated by studying other nucleopeptide compounds with related sequences.     

Effect of periodic feeding in sequencing batch reactor on substrate uptake and storage rates by a pure culture of Amaricoccus kaplicensis

A pure culture of Amaricoccus kaplicensis was aerobically cultured at a long culture residence time (Theta(C)>12d), under periodic acetate feeding in a sequencing batch reactor (SBR). The cycle length and, correspondingly, the volumetric organic load rate (vOLR) were varied in the range 4-24h and 0.76-0.12gCODl(-1)d(-1), respectively. The transient response of the microorganism to the acetate spike was investigated throughout batch tests, as a function of SBR cycle length and vOLR. In all tested conditions, a rapid transient response was observed, mainly due to acetate storage in the form of polyhydroxybutyrate, since growth (production of active biomass) played a minor role. Apart from this general trend, the maximum rates under transient conditions increased as the cycle length increased from 4 to 24h. In the SBR, the longest cycle also caused a decrease in floc size and settleability as well as an increase in the observed yield. The observed effect of SBR operating conditions on the physiological state of cells and their related transient response may have great significance on the performance of full scale activated sludge processes.     

Surface modification and patterning using low-energy ion beams: Si-O bond formation at the vacuum/adsorbate interface.

Modification of hydroxyl-terminated self-assembled monolayer (HO-SAM) surfaces by collision of low-energy (15 eV) hyperthermal Si(CH3)3+ ions is shown to lead to Si-O bond formation and terminal trimethylsilyl ether formation. Modification was verified by in situ mass spectrometry using chemical sputtering with CF3+ ions (70 eV), ex situ secondary ion mass spectrometric analysis (12 kV Ga+ primary ion beam), and through X-ray photoelectron spectroscopy by monitoring Si (2s). The nature of the surface modification was further established by analysis of synthetic SAM surfaces made up of mixtures of the trimethylsilyl-11-mercapto-1-undecane ether and various proportions of the hydroxyl-terminated mercaptan (11-mercapto-1-undecanol). These mixed surfaces, as well as the spectroscopic data, indicate that ca. 30% of the hydroxyl chains are covalently modified at saturation coverage. Analogous surface transformations are achieved using Si(CH3)2F+ and Si(CH3)2C6H5+.     

T c as a Function of Electron Doping in Mg10B2 Using Sc for Mg Substitution

We have studied the variation of superconducting critical temperature T _c as a function of electron doping in the Mg¹⁰B₂ system using Sc for Mg substitution. The critical temperature in the¹⁰B isotope substituted system Mg_{1? x} Sc _x ¹⁰B₂ increases by increasing the scandium content x in the range 0<x<0.012 up to 41.4 K, while the T _c of the natural boron system Mg_{1? x} Sc _x B₂ is nearly constant. The overall difference of T _c in Mg_{1? x} Sc _x B₂ as function of x between the natural B and ¹⁰B isotope system seems to indicate that the isotope effect shows large variations with electron doping as expected for the T _c enhancement driven by a shape resonance.