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By combining frontal polymerization and radical‐induced cationic polymerization, it was possible to cure thick samples of an epoxy monomer bleached by UV light. The effect of the relative amounts of cationic photoinitiator and radical initiator was thoroughly investigated and was related to the front's velocity and its maximum temperature. The materials obtained were characterized by quantitative conversion also in the deeper layers, not reached by UV light. © 2004 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 42: 2066–2072, 2004  相似文献   
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We discuss derivation‐like techniques for transforming one locally Hermitian partial ovoid of the Hermitian surface H(3,q2) into another one. These techniques correspond to replacing a regulus by its opposite in some naturally associated projective 3‐space PG(3,q) over a square root subfield. © 2006 Wiley Periodicals, Inc. J Combin Designs 15: 478–486, 2007  相似文献   
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A proposal for the Hamilton-Jacobi theory in the context of the covariant formulation of Hamiltonian systems is done. The current approach consists in applying Dirac’s method to the corresponding action which implies the inclusion of second-class constraints in the formalism which are handled using the procedure of Rothe and Scholtz recently reported. The current method is applied to the non-relativistic two-dimensional isotropic harmonic oscillator employing the various symplectic structures for this dynamical system recently reported.  相似文献   
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A multi-residue method has been developed for the determination of anabolic steroids in animal tissue. The analytes are extracted from tissue with methanol and the extract is subjected to two solid-phase extractions, one using a non-specific adsorbing material, such as graphitized carbon black (Carbopack B), and the other Amberlite CG-400 I in the OH form. This procedure allowed the neutral anabolics (testosterone, trenbolone and progesterone) to be isolated and separated from the acidic type (phenolic group), such as diethylstilbestrol, oestradiol, zeranol/zearalenone and their respective metabolites. The determination was effected using high-performance liquid chromatography with different detectors (ultraviolet, fluorimetric and electrochemical). Several analytical parameters were studied: chromatographic conditions, recoveries, evaporation step, solvent flow-rate, cartridges reusability, interference of plastic cartridges. For all the anabolics investigated the recoveries were greater than 83.6%.  相似文献   
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The proposal of hunting theH-particle taking advantage of antiproton annihilation at rest on3He is discussed. The obtained K* beam should allow one to obtain a flux ofΞ ? with momentum low enough to optimize the fusion probability (ΞN) to give anH. The experimental apparatus to detectH-events as the only missing mass of the fully reconstructed reaction¯p 3He →KKπ + H is the OBELIX Spectrometer at LEAR. A detailed Monte Carlo simulation of the overall acceptance of OBELIX for the above reaction is performed. The obtained final rate shows the feasibility of the experiment also in a not dedicated detector like OBELIX.  相似文献   
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New fluorinated, polyfunctional propenyl ether functionalized resins were synthesized, and their behavior in cationic photopolymerization was investigated. The photopolymerization proceeded efficiently with a high double‐bond conversion (>90%), giving rise to UV‐cured coatings characterized by low glass‐transition temperatures (?33 °C ≤ glass‐transition temperature ≤ ?15 °C) and hydrophobic surface properties. A fluorinated additive was also employed as a reactive additive in the cationic photopolymerization of trimethylolpropane tripropenyl ether, increasing the double‐bond conversion, polymer network flexibility, thermal stability, and surface hydrophobicity. © 2006 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 44: 6943–6951, 2006  相似文献   
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Summary Mercuric ions may be determined by titration with ethylenedithiodiacetic acid at a wavelength of 260 nm at any pH less than 1. The method is simple, rapid, and selective, and is applicable in solutions of high electrolyte concentration. Mercury(II) can be determined down to 1.5×10–5 M with a relative standard deviation less than 2%.
Zusammenfassung Quecksilber (II) läßt sich mit Äthylendithiodiessigsäure bei 260 nm und pH1 titrieren. Das Verfahren ist einfach, rasch und selektiv. Es läßt sich auch für Lösungen mit hoher Elektrolytkonzentration anwenden. Hg(II)-Konzentrationen über 1,5×10–5 M sind mit einer relativen Standardabweichung unter 2% bestimmbar.
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