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1.
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   
2.
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   
3.
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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4.
Stable polyacrylamide (polyAA)–montmorillonite adducts were prepared by two distinct processes: (1) free radical copolymerization of AA with alkaline clay previously treated with 2-(N-methyl-N,N-diethyl ammonium iodide)ethylacrylate (QD1) and (2) direct interactions of alkaline montmorillonite with various preformed copolymers of AA with QD1. The structure of the adducts as determined by Fourier transform infrared spectroscopy, thermogravimetric analysis, differential scanning calorimetry and X-ray diffraction was shown to consist of AA macromolecules inserted between lamellar layers whose spacing was larger than in the polymer-free clay. The polymer was strongly attached to the inorganic surfaces, probably due to cooperative formation of electrostatic bonding. The thermal stability of the organic polymers in the resulting complexes was substantially enhanced while the mobility of macromolecules decreased.  相似文献   
5.
Reaction of 1-oxo-2-formyl-3-dimethylamino-1H-naphtho[2,1-b]pyran with amidines, guanidine, O-methylisourea, S-methylisothiourea afforded 9-substituted 12-oxo-12H-naphtho[1′,2′:5,6]pyrano[2,3-d]pyrimidines. When the reaction with O-methylisourea was carried out in anhydrous pyridine, 10,20-dioxo-10H,20H-dinaphtho[1,2-e:1′,2′-e′][1,5]diazocino[2,3-b:6,7-b′]dipyran was formed.  相似文献   
6.
Communicated by Dominique Perrin  相似文献   
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8.
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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10.
Summary An ionized gas whose dynamics is dominated by charge exchange is considered. The following two problems are studied: the time behaviour of sinusoidal waves in a uniform equilibrium; the propagation in a bounded equilibrium of sinusoidal oscillations forced to the wall. It is shown, in particular, that the equilibria considered, not necessarily thermal equilibria, are stable for any form of the distribution function.
Sommario Si considera un gas ionizzato, non necessariamente in equilibrio termico, la cui dinamica sia dominata dal processo di scambio di carica, e si studiano i seguenti due problemi: evoluzione temporale di onde sinusoidali su un equilibrio uniforme; propagazione di oscillazioni sinusoidali forzate alla parete in un equilibrio spazialmente limitato. Si mostra in particolare la stabilitá degli equilibri per qualunque forma della funzione di distribuzione.


Research supported in part by C.N.R., G.N.F.M.  相似文献   
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