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181.
T.J. Holmquist J. Bradley A. Dwivedi D. Casem 《The European physical journal. Special topics》2016,225(2):343-354
This article presents the response of polymethyl methacrylate (PMMA) subjected to large strains, high strain rates, high pressures, a range in temperatures, and variations in the intermediate principal stress. Laboratory data from the literature, and new test data provided here, are used in the evaluation. The new data include uniaxial stress compression tests (at various strain rates and temperatures) and uniaxial stress tension tests (at low strain rates and ambient temperatures). The compression tests include experiments at ?ε= 13,000 s?1, significantly extending the range of known strain rate data. The observed behavior of PMMA includes the following: it is brittle in compression at high rates, and brittle in tension at all rates; strength is dependent on the pressure, strain, strain rate, temperature, and the intermediate principal stress; the shear modulus increases as the pressure increases; and it is highly compressible. Also presented are novel, high velocity impact tests (using high-speed imaging) that provide insight into the initiation and evolution of damage. Lastly, computational constitutive models for pressure, strength, and failure are presented that provide responses that are in good agreement with the laboratory data. The models are used to compute several ballistic impact events for which experimental data are available. 相似文献
182.
Small-angle X-ray scattering and rheological characterization of aqueous lignosulfonate solutions 总被引:1,自引:0,他引:1
Vainio U Lauten RA Serimaa R 《Langmuir : the ACS journal of surfaces and colloids》2008,24(15):7735-7743
Lignosulfonate is a colloidal polyelectrolyte widely used as a dispersant in various industrial applications and produced during chemical pulping of wood chips. Here we present a systematic small-angle X-ray scattering (SAXS) and rheological study of fractionated lignosulfonate (mass weighted molar mass M w 18 000 g/mol) dissolved in water and 0.2 M NaCl. The concentration range varied from semidilute to concentrated regime. SAXS intensity of all solutions followed the Porod law at all concentrations, which is a clear indication of a compact shape of the lignosulfonate particle. In water, below 10 mass % lignosulfonate, the average interparticle distance obtained from SAXS patterns relates to concentration via a power law with exponent -0.28. Deviation of the power law exponent from ideal -0.33 and a linear decrease in volume fraction normalized Porod constant as a function of concentration are taken as indications of self-association of lignosulfonate. In saline solutions at high lignosulfonate mass fractions the average distance between lignosulfonate particles was longer and the average particle size was larger than those in aqueous solutions. The intrinsic viscosity in saline solution also was larger than that in aqueous solution. Lignosulfonate solutions showed Newtonian viscosity, except at very high concentrations. The variation of the relative zero-shear viscosity eta(0),r) with concentration was interpreted with the Krieger-Dougherty equation. An oblate spheroid shape with an axial ratio of 3.5 describes the average shape of the lignosulfonate particles in saline solutions based on SAXS intensities, the size distribution obtained using gel permeation chromatography, and rheological characterization. The largest dimension of the particles was about 8 nm. SAXS and rheology studies as a function of temperature reveal indications of temperature-dependent self-association. 相似文献
183.
This article presents computed results of the U. S. Army Research Laboratory (ARL) 14.5 mm BS41 projectile impacting steel
targets with varying impact conditions. The ARL BS41 is a complex projectile that includes a soft metal jacket, lead filler,
inert powder and a high-strength tungsten carbide (WC) core. The WC core includes a nominal 6 wt% cobalt binder (WC-.06Co)
producing significant ductility in compression but very little in tension. Recent 3D numerical algorithm advancements and
a more accurate material model for WC produce computed results that are in good agreement with experimental results. The computed
results demonstrate the ability to reproduce several key observations: the stripping of the steel jacket, lead filler and
inert powder when impacting thin and thick steel targets; rigid body penetration of the WC core into thin and thick steel
targets for normal impact; severe fracture and fragmentation of the core when impacting obliquely; and core fracture due to
a yaw angle at impact. The computed results may also explain why the core fractures at low obliquities and shatters at high
obliquities. Experimental data are also discussed and compared to the computed results. 相似文献
184.
Ari Lehmusvuori Ulla KarhunenAntti-Heikki Tapio Urpo LamminmäkiTero Soukka 《Analytica chimica acta》2012
We introduce a switchable lanthanide luminescence reporter technology based closed-tube PCR for the detection of specific target DNA sequence. In the switchable lanthanide chelate complementation based reporter technology hybridization of two nonfluorescent oligonucleotide probes to the adjacent positions of the complementary strand leads to the formation of a highly fluorescent lanthanide chelate complex. The complex is self-assembled from a nonfluorescent lanthanide chelate and a light-harvesting antenna ligand when the reporter molecules are brought into close proximity by the oligonucleotide probes. Outstanding signal-to-background discrimination in real-time PCR assay was achieved due to the very low background fluorescence level and high specific signal generation. High sensitivity of the reporter technology allows the detection of a lower concentration of amplified DNA in the real-time PCR, resulting in detection of the target at the earlier amplification cycle compared to commonly used methods. 相似文献
185.
Distribution of counterions around lignosulfonate macromolecules in different polar solvent mixtures
Vainio U Lauten RA Haas S Svedström K Veiga LS Hoell A Serimaa R 《Langmuir : the ACS journal of surfaces and colloids》2012,28(5):2465-2475
Lignosulfonate is a colloidal polyelectrolyte that is obtained as a side product in sulfite pulping. In this work we wanted to study the noncovalent association of the colloids in different solvents, as well as to find out how the charged sulfonate groups are organized on the colloid surface. We studied sodium and rubidium lignosulfonate in water-methanol mixtures and in dimethyl formamide. The number average molecular weights of the Na- and Rb-lignosulfonate fractions were 7600 g/mol and 9100 g/mol, respectively, and the polydispersity index for both was 2. Anomalous small-angle X-ray scattering (ASAXS) was used for determining the distribution of counterions around the Rb-lignosulfonate macromolecules. The scattering curves were fitted with a model constructed from ellipsoids of revolution of different sizes. Counterions were taken into account by deriving an approximative formula for the scattering intensity of the Poisson-Boltzmann diffuse double layer model. The interaction term between the spheroidal particles was estimated using the local monodisperse approximation and the improved Hayter-Penfold structure factor given by the rescaled mean spherical approximation. Effective charge of the polyelectrolyte and the local dielectric constant of the solvent close to the globular polyelectrolyte were followed as a function of the methanol content in the solvent and lignosulfonate concentration. The lignosulfonate macromolecules were found to aggregate noncovalently in water-methanol mixtures with increasing methanol or lignosulfonate content in a specific directional manner. The flat macromolecule aggregates had a nearly constant thickness of 1-1.4 nm, while their diameter grew when counterion association onto the polyelectrolyte increased. These results indicate that the charged groups in lignosulfonate are mostly at the flat surfaces of the colloid, allowing the associated lignosulfonate complexes to grow further at the edges of the complex. 相似文献
186.
Subtype selectivity and flexibility of ionotropic glutamate receptors upon antagonist ligand binding
Pentikäinen U Settimo L Johnson MS Pentikäinen OT 《Organic & biomolecular chemistry》2006,4(6):1058-1070
The binding modes of a set of known ionotropic glutamate receptor antagonist-ligands have been studied using homology modeling, molecular docking, molecular dynamics (MD) simulations and ab initio quantum mechanical calculations. The core structure of the studied ligands is the decahydroisoquinoline ring, which has a carboxylic acid group at position three and different negatively-charged substituents (R) at position six. The binding affinities of these molecules have been reported earlier. From the current study, the carboxylate group of the decahydroisoquinoline ring hydrogen bonds with Arg485, the amino group with Pro478 and Thr480, and the negatively charged substituent R interacts with the positively charged N-terminus of helix-F. The subtype selectivity of these ligands seems to be strongly dependent on the amino acid at position 650 (GluR2: leucine, GluR5: valine), which affects the conformation of the ligand and ligand-receptor interactions, but depends considerably on the size of the R-group of the ligand. In addition, the MD simulations also revealed that the relative positions of the S1 and S2 domains can alter significantly showing different "closure" and "rotational movements" depending on the antagonist-ligand that is bound. Accordingly, molecular docking of antagonist ligands into static crystal structures cannot sufficiently explain ligand binding and subtype selectivity. 相似文献
187.
Brinkmalm G Portelius E Öhrfelt A Mattsson N Persson R Gustavsson MK Vite CH Gobom J Månsson JE Nilsson J Halim A Larson G Rüetschi U Zetterberg H Blennow K Brinkmalm A 《Journal of mass spectrometry : JMS》2012,47(5):591-603
Amyloid precursor protein (APP) is the precursor protein to amyloid β (Aβ), the main constituent of senile plaques in Alzheimer's disease (AD). Endogenous Aβ peptides reflect the APP processing, and greater knowledge of different APP degradation pathways is important to understand the mechanism underlying AD pathology. When one analyzes longer Aβ peptides by low-energy collision-induced dissociation tandem mass spectrometry (MS/MS), mainly long b-fragments are observed, limiting the possibility to determine variations such as amino acid variants or post-translational modifications (PTMs) within the N-terminal half of the peptide. However, by using electron capture dissociation (ECD), we obtained a more comprehensive sequence coverage for several APP/Aβ peptide species, thus enabling a deeper characterization of possible variants and PTMs. Abnormal APP/Aβ processing has also been described in the lysosomal storage disease Niemann-Pick type C and the major large animal used for studying this disease is cat. By ECD MS/MS, a substitution of Asp7 → Glu in cat Aβ was identified. Further, sialylated core 1 like O-glycans at Tyr10, recently discovered in human Aβ (a previously unknown glycosylation type), were identified also in cat cerebrospinal fluid (CSF). It is therefore likely that this unusual type of glycosylation is common for (at least) species belonging to the magnorder Boreoeutheria. We here describe a detailed characterization of endogenous APP/Aβ peptide species in CSF by using an online top-down MS-based method. 相似文献