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ABSTRACT

A modified hyaluronic acid (HA) biopolymer was synthesized that can be photocrosslinked to form a stable hydrogel. The chemical and physical properties including the amount of modification of the polymer with methacrylate anhydride, the viscosity of the modified biopolymer, and the solute diffusion characteristics of the polymer have been determined.  相似文献   
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Abstract Complete information is usually assumed in harvesting models of marine and terrestrial resources. In reality, however, complete information never exists. Fish and wildlife populations often fluctuate unpredictably in numbers, and measurement problems are frequent. In this paper, we analyze a time‐discrete fishery model that distinguishes between uncertain natural growth and measurement error and in which exploitation takes place in an unregulated manner. Depending on the parameterization of the model and at which point of time uncertainty is resolved, it is shown that expected harvest under ecological uncertainty may be below or above that of the benchmark model with no uncertainty. On the other hand, when stock measurement is uncertain, expected harvest never exceeds the benchmark level. We also demonstrate that the harvesting profit, or rent, under uncertainty may be above that of the benchmark situation of complete information. In other words, less information may be beneficial for the fishermen.  相似文献   
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A flash photolysis–resonance fluorescence technique was used to investigate the kinetics of the OH(X2Π) radical and O(3P) atom‐initiated reactions with CHI3 and the kinetics of the O(3P) atom‐initiated reaction with C2H5I. The reactions of the O(3P) atom with CHI3 and C2H5I were studied over the temperature range of 296 to 373 K in 14 Torr of helium, and the reaction of the OH (X2Π) radical with CHI3 was studied at T = 298 K in 186 Torr of helium. The experiments involved time‐resolved resonance fluorescence detection of OH (A2Σ+ → X2Π transition at λ = 308 nm) and of O(3P) (λ = 130.2, 130.5, and 130.6 nm) following flash photolysis of the H2O/He, H2O/CHI3/He, O3/He, and O3/C2H5I/He mixtures. A xenon vacuum UV (VUV) flash lamp (λ > 120 nm) served as a photolysis light source. The OH radicals were produced by the VUV flash photolysis of water, and the O(3P) atoms were produced by the VUV flash photolysis of ozone. Decays of OH radicals and O(3P) atoms in the presence of CHI3 and C2H5I were observed to be exponential, and the decay rates were found to be linearly dependent on the CHI3 and C2H5I concentrations. Measured rate coefficients for the reaction of O(3P) atoms with CHI3 and C2H5I are described by the following Arrhenius expressions (units are cm3 s?1): kO+C2H5I(T) = (17.2 ± 7.4) × 10?12 exp[?(190 ± 140)K/T] and kO+CHI3(T) = (1.80 ± 2.70) × 10?12 exp[?(440 ± 500)K/T]; the 298 K rate coefficient for the reaction of the OH radical with CHI3 is kOH+CHI3(298 K) = (1.65 ± 0.06) × 10?11 cm3 s?1. The listed uncertainty values of the Arrhenius parameters are 2σ‐standard errors of the calculated slopes by linear regression.  相似文献   
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DFT calculations on a [N(SiH2CH2PH2)2]MH3 model (M = Ru and Os) of experimentally known compounds show that the three H have different bonding modes for Ru (H + H2) and for Os (three independent H). Calculation shows that the Ru(H)(H2) compound adds H2 to give an RuH(H2)2 substructure; the Os(H)2 species adds H2 to give the Os(H)3(H2) substructure. The impact of these intramolecular redox processes on bond lengths is discussed, as are attempts to provide an improved computational model of P(alkyl) n without the introduction of additional alkyl atoms.  相似文献   
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