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51.
Using a minimal model based on the phase-field-crystal formalism, we study the coupling between the density and magnetization in ferromagnetic solids. Analytical calculations for the square phase in two dimensions are presented and the small deformation properties of the system are examined. Furthermore, numerical simulations are conducted to study the influence of an external magnetic field on various phase transitions, the anisotropic properties of the free energy functional, and the scaling behaviour of the growth of the magnetic domains in a crystalline solid. It is shown that the energy of the system can depend on the direction of the magnetic moments, with respect to the crystalline direction. Furthermore, the growth of the magnetic domains in a crystalline solid is studied and is shown that the growth of domains is in agreement with expected behaviour.  相似文献   
52.
Two kinds of bio‐resourced reactive diluents have been synthesized from linseed oil. The prepared epoxidized linseed oil (ELO) and the cyclocarbonated linseed oil (CLO) were separately blended with a petroleum‐based tetra‐functional epoxy resin (TGDDM) to improve its processability and to overcome the brittleness of the thermoset network therefrom. The linseed oil modifications were spectrally established, and processability improvement of the resin blends was rheologically confirmed. The curing of samples was studied by differential scanning calorimetry, and their mechanical properties (ie, tensile, flexural, fracture toughness, and adhesion) were investigated as well. Scanning electron microscopy images were obtained to reconfirm the toughness improvement of the modified thermosets. In contrast of the epoxidized soybean oil (ie, the most conventionally studied bio‐based reactive diluent), ELO and CLO had no negative effects on the thermoset material characteristics. They improved properties such as tensile strength (up to 43.2 MPa), fracture toughness (1.1 MPa m1/2), and peel‐adhesion strength (4.5 N/25 mm). It was concluded that ELO and CLO were efficient reactive diluents to be used in formulations of polymer composites, surface coatings, and structural adhesives based on epoxy resins.  相似文献   
53.
A new stereospecific synthesis of lysophosphatidylcholines is reported. The sequence relies on orthogonal protection of hydroxyl groups derived from glyceric acid, using fluorenylmethylcarbonate versus tetrahydropyranyl ether functions, that allow regiospecific introduction of substituents to obtain the target phospholipid compound.  相似文献   
54.
This study proposes a novel and simple in-house design of a nanoparticle tracking analysis (NTA) device for the online characterization of nanoparticles in an aqueous solution. The particle size distribution of two sets of model nanoparticles, for example, transparent (SiO2) and opaque (TiO2) materials with respect to water as a dispersion medium could be successfully analyzed. Experiments are conducted using two different laser wavelengths of 632.8 (red) and 510 nm (green) and a range of concentrations. The accuracy of the green laser is larger compared to the red laser for all particle concentrations used. The measured average diameter using the presented in-house NTA setup is in the acceptable range compared to the electron microscopy data. The average diameter of the transparent (SiO2) and opaque (TiO2) samples is calculated as 36.29 and 27.26 nm using NTA, 36.44 and 27.8 nm analyzing field emission scanning electron microscopy images, and 23.97 and 19.7 nm analyzing transmission electron microscopy images. In the new viewing sample holder, nanoparticles undergo mere Brownian motion with no bulk drift velocity. The effect of solid concentration and wavelength of the laser light on the performance of the NTA sensor is investigated, and the optimal concentration range for model particles is reported.  相似文献   
55.
A protocol has been developed for the diastereoselective synthesis of dispiro[tetrahydroquinoline‐bis(2,2‐dimethyl[1,3] dioxane‐4,6‐dione)] derivatives via a one‐pot domino multicomponent reaction of arylamines, aromatic aldehydes, and Meldrum's acid for the first time. The products, with remarkable diastereoselectivity, were successfully synthesized in acetic acid media in ambient temperature along with the suggested mechanism through combination of domino Knoevenagel, Michael, and Diels–Alder reactions. The products have been characterized by IR, mass, 1H NMR, 13C NMR spectroscopy, and elemental analyses. The stereoselectivity of compounds was established with crystallography and NMR spectroscopy.  相似文献   
56.
A heterogeneous catalyst was synthesized by immobilizing Mo(CO)3 in a UiO‐66 metal–organic framework. The benzene ring of the organic linker in UiO‐66 was modified via liquid‐phase deposition of molybdenum hexacarbonyl, Mo(CO)6, as starting precursor to form the (arene)Mo(CO)3 species inside the framework. The structure of this catalyst was characterized using X‐ray diffraction, and chemical integrity was confirmed using Fourier transform infrared and diffuse reflectance UV–visible spectroscopic methods. The metal content was analysed with inductively coupled plasma. Field emission scanning electron microscopy was used to measure particle size and N2 adsorption measurements to characterize the specific surface area. This catalytic system was efficiently applied for epoxidation of alkenes and oxidation of sulfides. The Mo‐containing metal–organic framework was reused several times without any appreciable loss of its efficiency.  相似文献   
57.
In this article, we present a constructive method for computing the frame coefficients of finite wavelet frames over prime fields using tools from computational harmonic analysis and group theory.  相似文献   
58.
A glassy carbon electrode (GCE) is modified with platinum nanoparticle (PtNPs) decorated multiwalled carbon nanotube (MWCNT). The modified electrode is applied for the determination of ceftriaxone (CFX) in the presence of lidocaine. Different methods were used to characterize the surface morphology of the modified electrode. The electrochemical behavior of CFX was investigated at GCE, MWCNT/GCE and PtNPs/MWCNT/GCE. A factorial-based response-surface methodology was used to find out the optimum conditions with minimum number of experiments. Under the optimized conditions, oxidation peak currents increased linearly with CFX concentration in the range of 0.01–10.00 μM with a detection limit of 9.01 nM. The results prove that the modified electrode is also suitable for the determination of CFX in pharmaceutical and clinical preparations.  相似文献   
59.
The solvent effect has been studied in this research for the interaction of the $ {\text{VO}}_{2}^{ + } $ VO 2 + cation with trans-1,2-diaminocyclohexane-N, N, N′, N′- tetraacetic acid monohydrate at T = 298 K, I = 0.10 mol·dm?3 sodium perchlorate, and in the range of 0–45 % water + methanol mixtures. UV absorbance data as a function of pH and dissociation constants, obtained from potentiometric titrations, were used for the determination of stability constants. The Kamlet–Abboud–Taft (KAT) model has been investigated for a plausible interpretation and calculation of the linear solvation energy relationship coefficient contribution to the formation of three species VO2H2L, VO2HL? and VO2L2?, which were identified in this work.  相似文献   
60.
A novel mixed-ligand complex of [In(Me-phen)Cl3(DMSO)] (1) was acquired and specified via spectral approaches (IR, UV–Vis, 1H-NMR, and luminescence), thermal evaluation such as thermogravimetric, differential thermal analyses, and single-crystal X-ray diffraction. In this study, we have also reported the nanosize of [In(Me-phen)Cl3(DMSO)] (1) that has been synthesized via the sonochemical process. Characterization of nanoparticle (1) was carried out via X-ray powder diffraction, scanning electron microscopy, and Fourier transform infrared spectroscopy. The sample size assembled via the sonochemical approach was approximately 20 nm. Also, a novel screen-printed electrode modified with indium nanocomplex (In NC/SPE) was developed. An electrochemical examination of the adjusted electrode in addition to its efficiency in dopamine electro-oxidation is explained. It was proven that dopamine oxidation at adjusted electrode surface takes place at 150 mV potential less positive compared to an unadjusted screen-printed electrode. The relevant detection limit for dopamine was 2.0 × 10−7 M via differential pulse voltammetry. Moreover, the adjusted electrode was utilized to simultaneously determine dopamine and acetylcholine. Lastly, the adjusted electrode was utilized to determine dopamine and acetylcholine within real specimens.  相似文献   
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