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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.
A study was performed on dual curing systems based on UV curing of reactive unsaturations (acrylic double bonds) and successive alkoxysilane group condensation. The systems were obtained by mixing a typical epoxy acrylic resin with different amounts of monomers containing alkoxysilane groups (3-methacryloyloxypropyltrimethoxysilane, MEPTS, and 3-mercaptopropyltrimethoxysilane, MPTS) in the presence of a photoinitiator and a condensation catalyst. After UV curing, the kinetics of the alkoxysilane group condensation was followed by Fourier Transform Infrared Spectroscopy (FTIR) analysis at different temperatures and water vapour pressures. Higher condensation rates were obtained in the systems containing MPTS with respect to the MEPTS system. Also the adhesion on glass sheets was better in the presence of MPTS with respect to MEPTS. These results were attributed to the different structures and to the different crosslinking density obtained in the presence of the two monomers. Wetting tension, Attenuated Total Reflectance (ATR-FTIR) and X-Ray Photoelectron Spectroscopy (XPS) measurements are in agreement with these conclusions.  相似文献   
4.
We consider a SDE with a smooth multiplicative non-degenerate noise and a possibly unbounded Hölder continuous drift term. We prove the existence of a global flow of diffeomorphisms by means of a special transformation of the drift of Itô-Tanaka type. The proof requires non-standard elliptic estimates in Hölder spaces. As an application of the stochastic flow, we obtain a Bismut-Elworthy-Li type formula for the first derivatives of the associated diffusion semigroup.  相似文献   
5.
The cationic photopolymerization of oxetane‐based systems containing silicon monomers was investigated. For this purpose, three new silicon‐containing oxetane monomers were synthesized through a simple and straightforward synthetic method. The silicon‐containing monomers were added to a typical oxetane resin, 3,3′‐[oxydi(methylene)]bis(3‐ethyloxetane), in concentrations of 1–5 wt %. They exploited a certain surface tension effect without affecting the rate of polymerization. Enrichment only on the air side was achieved, which induced hydrophobicity in the photocured films, depending on the monomer structure and concentration. © 2004 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 42: 1415–1420, 2004  相似文献   
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New carbazole monomers were synthesized and their cationic photopolymerization investigated. The monomers contain in each molecule two pendant carbazole groups and two functional groups reactive towards cationic photopolymerization. The investigated reactive groups were epoxy, oxetane or vinyl ether. Each type of monomer contains a spacer group namely ethylene oxide segment. The UV curing kinetics of the different monomers was monitored by real time FT-IR (RT-FTIR) analysis and the thermal properties evaluated by DSC.  相似文献   
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9.
This Note is concerned with the properties of solutions to a linear evolution equation perturbed by a cylindrical Lévy process. It turns out that solutions, under rather weak requirements, do not have a càdlàg modification. Some natural open questions are also stated.  相似文献   
10.
In this paper we prove global bounds on the spatial gradient of viscosity solutions to second order linear and nonlinear parabolic equations in (0,T)×RN(0,T)×RN. Our assumptions include the case that the coefficients be both unbounded and with very mild local regularity (possibly weaker than the Dini continuity), the estimates only depending on the parabolicity constant and on the modulus of continuity of coefficients (but not on their LL-norm). Our proof provides the analytic counterpart to the probabilistic proof used in Priola and Wang (2006) [35] (J. Funct. Anal. 2006) to get this type of gradient estimates in the linear case. We actually extend such estimates to the case of possibly unbounded data and solutions as well as to the case of nonlinear operators including Bellman–Isaacs equations. We investigate both the classical regularizing effect (at time t>0t>0) and the possible conservation of Lipschitz regularity from t=0t=0, and similarly we prove global Hölder estimates under weaker assumptions on the coefficients. The estimates we prove for unbounded data and solutions seem to be new even in the classical case of linear equations with bounded and Hölder continuous coefficients. Applications to Liouville type theorems are also given in the paper. Finally, we compare in an appendix the analytic and the probabilistic approach discussing the analogy between the doubling variables method of viscosity solutions and the probabilistic coupling method.  相似文献   
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