Effect of Hydration on Silk Film Material Properties

Effects of hydration on silk fibroin film properties were investigated for water‐annealed and MeOH‐treated samples. Hydration increased thickness by 60% for MeOH‐immersed films, while water‐annealed samples remained constant. MeOH‐immersed films showed an 80% mass loss due to water, while water‐annealed lost only 40%. O₂ permeability was higher in MeOH‐immersed films with Dk values of 10^?10 (mL O₂ · cm) · (cm^?1 · s^?1 · mmHg^?1), while those of water‐annealed films reached only one fifth of this value. All films showed a decrease in Young's modulus and increased plastic deformation by two orders of magnitude when submerged in saline solution. FT‐IR showed that β‐sheet content in water‐annealed films increased with increasing water vapor pressure, while MeOH‐immersed films showed no change.

     

Total synthesis of 3,3-difluorinated 1-deoxynojirimycin analogues

Difluorination of 1-deoxynojirimycin at position C(3) creates a competitive inhibitor 15 of 10 times higher activity against an α-glucosidase than the parent compound. Its screening against a panel of human cell lines showed a low cytotoxicity therefore making this compound an interesting candidate for further clinical investigations.     

Isotope ratio monitoring gas chromatography/Mass spectrometry of D/H by high temperature conversion isotope ratio mass spectrometry

Of all the elements, hydrogen has the largest naturally occurring variations in the ratio of its stable isotopes (D/H). It is for this reason that there has been a strong desire to add hydrogen to the list of elements amenable to isotope ratio monitoring gas chromatography/mass spectrometry (irm-GC/MS). In irm-GC/MS the sample is entrained in helium as the carrier gas, which is also ionized and separated in the isotope ratio mass spectrometer (IRMS). Because of the low abundance of deuterium in nature, precise and accurate on-line monitoring of D/H ratios with an IRMS requires that low energy helium ions be kept out of the m/z 3 collector, which requires the use of an energy filter. A clean mass 3 (HD(+.)) signal which is independent of a large helium load in the electron impact ion source is essential in order to reach the sensitivity required for D/H analysis of capillary GC peaks. A new IRMS system, the DELTA(plus)XL(trade mark), has been designed for high precision, high accuracy measurements of transient signals of hydrogen gas. It incorporates a retardation lens integrated into the m/z 3 Faraday cup collector. Following GC separation, the hydrogen bound in organic compounds must be quantitatively converted into H(2) gas prior to analysis in the IRMS. Quantitative conversion is achieved by high temperature conversion (TC) at temperatures >1400 degrees C. Measurements of D/H ratios of individual organic compounds in complicated natural mixtures can now be made to a precision of 2 per thousand (delta notation) or, better, with typical sample amounts of approximately 200 ng per compound. Initial applications have focused on compounds of interest to petroleum research (biomarkers and natural gas components), food and flavor control (vanillin and ethanol), and metabolic studies (fatty acids and steroids). Copyright 1999 John Wiley & Sons, Ltd.     

Mass Measurements of 114–124,130Xe with the ISOLTRAP Penning Trap Spectrometer

The masses of the xenon isotopes with 114≤A≤123 were directly measured for the first time. The experiments were carried out at the ISOLTRAP triple trap spectrometer at the on-line mass separator ISOLDE/CERN. A mass resolving power of the Penning trap spectrometer of m/Δm≈500 000 was chosen and an accuracy of δm≈12keV for all investigated Xe isotopes was achieved. An atomic mass evaluation was performed and the results of this adjustment are compared with theoretical predictions. The new results for the xenon isotopes and their effects on neighboring nuclides are discussed within the two-neutron separation energy picture. This revised version was published online in July 2006 with corrections to the Cover Date.     

Determination of90Sr in environmental samples with resonance ionization spectroscopy in collinear geometry

A new, fast technique for trace analysis of the radioactive isotopes⁸⁹Sr and⁹⁰Sr in environmental samples has been developed. Conventional mass separation is combined with resonance ionization spectroscopy in collinear geometry, which provides high selectivity and sensitivity. In addition, a chemical separation procedure for sample preparation has been developed. The described technique was used to determine the⁹⁰Sr content in 870 m³ air samples collected near Munich during and shortly after the Chernobyl reactor accident in April 1986. The content of⁹⁰Sr was measured to be 1.4 mBq per m³, corresponding to 1.6 × 10⁹ atoms of⁹⁰Sr per sample. This value is in good agreement with the results of radiochemical measurements.This publication comprises part of the Dissertations of J. Stenner and K. Zimmer     

Radical products of the oxidation of 2,2-diacyl-1-arylhydrazines with the system Pb(OAc)4-CF3COOH-CH2Cl2

Summary The oxidation of 2,2-Diacyl-1-arylhydrazines1a–l with the system Pb(OAc)₄-CF₃COOH-CH₂Cl₂ led to the formation of two types of radical products. Phenazinium cation radicals5a–h were formed from 2,2-diacyl-1-arylhydrazines1a–h, while hydrazyl radicals2i–l were observed to be the only radical products of the oxidation of1i–l. The generated radicals are characterized by their EPR parameters.

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Radikalische Produkte der Oxidation von 2,2-Diacyl-1-arylhydrazinen mit dem System Pb(OAc)₄-CF₃COOH-CH₂Cl₂

Zusammenfassung Die Oxidation der 2,2-Diacyl-1-arylhydrazine1a–l mit dem System Pb(OAc)₄-CF₃COOH-CH₂Cl₂ führte zu zwei unterschiedlichen Typen von Radikalen. Aus den 2,2-Diacyl-1-arylhydrazinen1a–h werden die Phenaziniumkationenradikale5a–h gebildet, während nach Oxidation von1i–l die entsprechenden Hydrazyle2i–l als einzige Radikalprodukte nachweisbar waren. Die erzeugten Radikale wurden durch ihre EPR-Parameter charakterisiert.

     

Flavour tagging of parton jets and separation of parton subprocesses in hard proton-proton collisions at the ISR

High energy proton-proton interactions yielding a single trigger particle with large transverse momentum give rise to a four-jet event structure with two transverse jets and two jets along the beam direction. The transverse jets are due to the fragmentation of point like scattered partons. It is shown that the quantum numbers of triggering charged pions and positive kaons are correlated with the flavour of the scattered parent parton; thus one can enhance data samples with a particular flavour of a scattered parton. The analysis, which is independent of detailed model calculations, exploits (a) the identification of the leading particles in the trigger jets (trigger particles), (b) the measurement of their relative production rates, (c) short range quantum number correlations within the trigger jets, and (d) long range correlations between leading particles from different jets. The data were obtained at \(\sqrt s \) =62 GeV with the Split Field Magnet detector at the CERN ISR.     

Highp T hadrons as leading particles in jets produced at the ISR

The density of charged particles near a single highp _T trigger particle in proton-proton collisions has been studied with the SFM detector at the CERN-ISR. It is shown that:—the secondaries cluster in a jet-like manner about the trigger particle; —the momentum distributions in this trigger jet can be unambiguously separated from the spectator background distributions;—the momentum distributions in this trigger jet can be unambiguously separated from the spectator background distributions;—the momentum component transverse to the jet direction is exponentially damped;—the width of the transverse distributions increases with the momentum component along the jet;—the fractional longitudinal momentum density depends strongly on the trigger transverse momentum and scales with \(x_T = {{2p_T } \mathord{\left/ {\vphantom {{2p_T } {\sqrt s }}} \right. \kern-0em} {\sqrt s }}\) . All these findings support the hard constituent scattering origin of highp _T hadrons.