687 research outputs found

    Raman spectroscopy, a non-destructive solution to the study of glass and its alteration

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    This paper presents the potential of Raman spectroscopy, a non-destructive technique which can be applied in-situ, for the analyses of glass and their alteration. Recent analytical developments are summarised for different glass composition and practical examples are given. The paper describes how to extract compositional information from the glass, first based on the spectra profile to distinguish rapidly alkali silicate from alkaline-earth alkali silicate and lead alkali silicate glass, then using the spectral decomposition and correlations to extract quantitative data. For alkali silicate glasses, that are most prone to alteration, the spectral characteristics are described to interpret the alteration process (selective leaching or dissolution of the glass) from the Raman spectra of the altered glass. These developments have greatly widened the potential of the technique and supplement well its ability to measure the thickness of the altered layer and identify the crystalline deposits

    Low Energy States of 3181Ga50^{81}_{31} Ga_{50} : Elements on the Doubly-Magic Nature of 78^{78}Ni

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    Excited levels were attributed to 3181^{81}_{31}Ga50_{50} for the first time which were fed in the β\beta-decay of its mother nucleus 81^{81}Zn produced in the fission of nat^{nat}U using the ISOL technique. We show that the structure of this nucleus is consistent with that of the less exotic proton-deficient N=50 isotones within the assumption of strong proton Z=28 and neutron N=50 effective shell effects.Comment: 4 pages, REVTeX 4, 5 figures (eps format

    Photodegradation and biodegradation of poly(lactic) acid containing orotic acid as a nucleation agent

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    Orotic acid is a natural heterocyclic compound that acts as a nucleation agent in poly(lactic acid) (PLA). PLA materials with increasing orotic acid content were prepared and characterized. It was found that crystallinity of about 28% was reached with 0.3% content of the agent. Further enhancement in the content of the agent did not provoke any additional significant increase of crystallinity. Subsequently, it was investigated whether the orotic acid content affected photodegradation of PLA and, in the next phase, its biodegradation. The results of rheological measurements showed that the compound slightly accelerates photodegradation of the material, which was accompanied by the cleavage of PLA chains. Previous photodegradation was shown to accelerate the subsequent biodegradation by shortening the lag phase of the process, where the explanation is probably in the reduction of the polymer molecular weight during the photodegradation. Moreover, the presence of orotic acid in both initial and photodegraded samples was found to influence biodegradation positively by shortening the lag phase and increasing the observed maximal rate of the biodegradation. © 2019 by the authors.Tomas Bata University in Zlin, Internal Grant Agency [IGA/FT/2018/009, IGA/FT/2019/011

    Natural deep eutectic solvents as thermostabilizer for Humicola insolens cutinase

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    As a new generation of green solvents, deep eutectic solvents (DESs) are considered a promising alternative to current harsh organic solvents and find application in many chemical processing methods such as extraction and synthesis. DESs, normally formed by two or more components via various hydrogen bond interactions, offer high potential as medium for biocatalysis reactions where they can improve efficiency by enhancing substrate solubility and the activity and stability of the enzymes. In the current study, the stabilization of Humicola insolens cutinase (HiC) in natural deep eutectic solvents (NADESs) was assessed. The best hydrogen bond donor among sorbitol, xylitol, erythritol, glycerol and ethylene glycol, and the best acceptor among betaine, choline chloride, choline acetate, choline dihydrogen citrate and tetramethylammonium chloride, were selected, evaluating binding energies and molecular orientations through molecular docking simulations, and finally used to prepare NADES aqueous solutions. The effects of component ratio and NADES concentration on HiC thermostability at 90 degrees C were also investigated. The choline dihydrogen citrate:xylitol, in a 1:1 ratio with a 20 wt% concentration, was selected as the best combination in stabilizing HiC, increasing its half-life three-fold

    Search for Fingerprints of Tetrahedral Symmetry in 156Gd^{156}Gd

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    Theoretical predictions suggest the presence of tetrahedral symmetry as an explanation for the vanishing intra-band E2-transitions at the bottom of the odd-spin negative parity band in 156Gd^{156}Gd. The present study reports on experiment performed to address this phenomenon. It allowed to determine the intra-band E2 transitions and branching ratios B(E2)/B(E1) of two of the negative-parity bands in 156Gd^{156}Gd.Comment: presented by Q.T. Doan at XLII Zakopane School of Physics: Breaking Frontiers: Submicron Structures in Physics and Biology, May 2008. 5 pages, minor corrections. To be published in the proceeding

    Study of the N=50 major shell effect close to 78^{78}Ni : First evidence of a weak coupling structure in 83_32^{83}\_{32}Ge_51\_{51} and three-proton configuration states in 81_31^{81}\_{31}Ga_50\_{50}

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    New levels were attributed to 81_31^{81}\_{31}Ga_50\_{50} and 83_32^{83}\_{32}Ge_51\_{51} which were fed by the β\beta-decay of their respective mother nuclei 81_30^{81}\_{30}Zn_51\_{51} and 83_31^{83}\_{31}Ga_52\_{52} produced by fission at the "PARRNe" ISOL set-up installed at the Tandem accelerator of the Institut de Physique Nucl\'eaire, Orsay. We show that the low energy structure of 81_31^{81}\_{31}Ga_50\_{50} and 83_32^{83}\_{32}Ge_51\_{51} can easily be explained within the natural hypothesis of a strong energy gap at N=50 and a doubly-magic character for 78^{78}Ni.Comment: 2 pages, pdf file, To be published in the Proceedings of "International Symposium on Structure of Exotic Nuclei and Nuclear Forces (SENUF 06)", March 2006, Tokyo, Japa
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