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41.
Thomas B. Goudoulas Eleftherios G. Kastrinakis Stavros G. Nychas 《Rheologica Acta》2007,46(3):357-367
Aspects of dense lignite–water slurries (LWS) rheology were investigated using controlled stress and controlled strain rheometers
with parallel disks and Couette geometries. During the preparation of the slurries, the achieved solids volume fractions were
up to 0.425 and the particle size distributions were polydispersed with sizes up to 300 μm. In the ascending parts of consecutive
flow loops, a slope transition of the flow curve was observed and studied in relation to the solids volume fraction. The obtained
results with the different geometries and rheometers were qualitatively the same. By following the model proposed by Cheng
(Rheol Acta 42:372–382, 2003) for thixotropic fluids, and taking into account the yield stress appearance, a suitable correlation for LWS is proposed,
which is consistent with the experimental flow curves. 相似文献
42.
Andrew W. Smyth Sami F. Masri Elias B. Kosmatopoulos Anastassios G. Chassiakos Thomas K. Caughey 《International Journal of Non》2002,37(8):378-1451
Adaptive estimation procedures have gained significant attention by the research community to perform real-time identification of non-linear hysteretic structural systems under arbitrary dynamic excitations. Such techniques promise to provide real-time, robust tracking of system response as well as the ability to track time variation within the system being modeled. An overview of some of the authors’ previous work in this area is presented, along with a discussion of some of the emerging issues being tackled with regard to this class of problems. The trade-offs between parametric-based modeling and non-parametric modeling of non-linear hysteretic dynamic system behavior are discussed. Particular attention is given to (1) the effects of over- and under-parameterization on parameter convergence and system output tracking performance, (2) identifiability in multi-degree-of-freedom structural systems, (3) trade-offs in setting user-defined parameters for adaptive laws, and (4) the effects of noise on measurement integration. Both simulation and experimental results indicating the performance of the parametric and non-parametric methods are presented and their implications are discussed in the context of adaptive structures and structural health monitoring. 相似文献
43.
We develop the axisymmetric Synthetic Schlieren technique to study the wake of a microscale sphere settling through a density
stratification. A video-microscope was used to magnify and image apparent displacements of a micron-sized random-dot pattern.
Due to the nature of the wake, density gradient perturbations in the horizontal greatly exceed those in the vertical, requiring
modification of previously developed axisymmetric techniques. We present results for 780 and 383 μm spheres, and describe
the limiting role of noise in the system for a 157 μm sphere. This technique can be instrumental in understanding a range
of ecological and environmental oceanic processes on the microscale.
相似文献
King-Yeung Yick (Corresponding author)Email: |
Roman StockerEmail: |
Thomas PeacockEmail: |
44.
Pretransitional fluctuations in the isotropic phase of liquid crystalline and non‐liquid crystalline alkyl cyanobiphenyls have been investigated using light scattering and magnetic birefringence measurements. We find evidence for a virtual isotropic‐nematic phase transition in short‐chain alkyl cyanobiphenyls with no observable nematic phase. The measured temperature dependence of fluctuations is well‐described by mean‐field theory. Virtual phase transition temperatures extrapolated from separate light scattering and magnetic birefringence experiments are in good agreement. Landau–de Gennes model parameters for the compounds investigated are calculated from the experimental results. 相似文献
45.
Devrishi Goswami Srikripa Devarakonda Michael J. Chalmers Bruce D. Pascal Bruce M. Spiegelman Patrick R. Griffin 《Journal of the American Society for Mass Spectrometry》2013,24(10):1584-1592
Application of typical HDX methods to examine intrinsically disordered proteins (IDP), proteins that are natively unstructured and highly dynamic at physiological pH, is limited because of the rapid exchange of unprotected amide hydrogens with solvent. The exchange rates of these fast exchanging amides are usually faster than the shortest time scale (10 s) employed in typical automated HDX-MS experiments. Considering the functional importance of IDPs and their association with many diseases, it is valuable to develop methods that allow the study of solution dynamics of these proteins as well as the ability to probe the interaction of IDPs with their wide range of binding partners. Here, we report the application of time window expansion to the millisecond range by altering the on-exchange pH of the HDX experiment to study a well-characterized IDP; the activation domain of the nuclear receptor coactivator, peroxisome proliferator-activated receptor gamma coactivator-1 alpha (PGC-1α). This method enabled mapping the regions of PGC-1α that are stabilized upon binding the ligand binding domain (LBD) of the nuclear receptor peroxisome proliferator-activated receptor gamma (PPARγ). We further demonstrate the method’s applicability to other binding partners of the IDP PGC-1α and pave the way for characterizing many other biologically important ID proteins. Figure
? 相似文献
46.
Simultaneous grafting of 2-hydroxyethyl methacrylate and methyl methacrylate (3:1 and 3:2 mole ratios) onto insoluble collagen with ceric ammonium nitrate as initiator was attempted with a view to optimizing conditions for the preparation of hydrogels. The influence of monomer and initiator concentrations on the grafting reactions was investigated. The grafting results are discussed in the light of grafting efficiency and percentage of grafting. They were found to be lower when the 3:1 mole ratio of monomers was used. 相似文献
47.
The cure kinetics of epoxy based on the diglycidyl ether of bisphenol A (DGEBA) modified with different amounts of poly(acrylonitrile-butadiene-styrene) (ABS) and cured with 4,4′-diaminodiphenylsulfone (DDS) was investigated by employing differential scanning calorimetry (DSC). The curing reaction was followed by using an isothermal approach over the temperature range 150–180°C. The amount of ABS in the blends was 3.6, 6.9, 10 and 12.9 wt%. Blending of ABS in the epoxy monomer did not change the reaction mechanism of the epoxy network formation, but the reaction rate seems to be decreased with the addition of the thermoplastic. A phenomenological kinetic model was used for kinetic analysis. Activation energies and kinetic parameters were determined by fitting the kinetic model with experimental data. Diffusion control was incorporated to describe the cure in the latter stages, predicting the cure kinetics over the whole range of conversion. The reaction rates for the epoxy blends were found to be lower than that of the neat epoxy. The reaction rates decreased when the ABS contents was increased, due to the dilution effect caused by the ABS on the epoxy/amine reaction mixture. 相似文献
48.
The performance of four different reversed-phase columns which included a conventional C18 phase, a C18 polar-endcapped phase, an ether-linked phenyl polar-endcapped phase and a calixarene-bonded phase has been systematically compared for the separation of mixture of some water-soluble vitamins containing basic, neutral and acidic compounds of different polarities, as well as different functional groups at three pH levels and different proportions of buffer/methanol. The characteristics of water-soluble vitamins make this combination of compounds very useful as a test mixture to check column performance with real samples. Due to the physical and chemical differences between these compounds, the type of chosen column has a significant influence on the chromatographic behavior. Results of this comparison show that the C18 polar-endcapped phase was the most suitable for the separation of this group of vitamins. The presence of a polar group as an endcapping agent does not seem to influence the overall hydrophobic nature of the polar-endcapped stationary phases. At the same time, these phases displayed enhanced hydrogen bonding and silanol activity. 相似文献
49.
Chiara Saggese Charlotte M. Thomas Scott W. Wagnon Goutham Kukkadapu Song Cheng Dongil Kang S. Scott Goldsborough William J. Pitz 《Proceedings of the Combustion Institute》2021,38(1):415-423
Propanol and butanol isomers have received significant research attention as promising fuel additives or neat biofuels. Robust chemical kinetic models are needed that can provide accurate and efficient predictions of combustion performance across a wide range of engine relevant conditions. This study seeks to improve the understanding of ignition and combustion behavior of pure C3-C4 linear and iso-alcohols, and their blends with gasoline at engine-relevant conditions. In this work, a kinetic model with improved thermochemistry and reaction kinetics was developed based on recent theoretical calculations of H-atom abstraction and peroxy radical reaction rates. Kinetic model validations are reported, and the current model reproduces the ignition delay times of the C3 and C4 alcohols well. Variations in reactivity over a wide range of temperatures and other operating conditions are also well predicted by the current model. Recent ignition delay time measurements from a rapid compression machine of neat iso-propanol and iso-butanol [Cheng et al., Proc. Combust Inst. (2020)] and blends with a research grade gasoline [Goldsborough et al., Proc. Combust Inst. (2020)] at elevated pressure (20–40 bar) and intermediate temperatures (780–950 K) were used to demonstrate the accuracy of the current kinetic model at conditions relevant to boosted spark-ignition engines. The effects of alcohol blending with gasoline on the autoignition behavior are discussed. The current model captures the suppression of reactivity in the low-temperature and negative-temperature-coefficient (NTC) region when either isopropanol and isobutanol are added to a research grade gasoline. Sensitivity and reaction flux analysis were performed to provide insights into the relevant fuel chemistry of the C3-C4 alcohols. 相似文献
50.
Jorge R. Virus-Segovia Fernando Reyes Sandra Ruíz Jesús Martín Ignacio Fernndez-Pastor Carlos Justicia Mercedes de la Cruz Caridad Díaz Thomas A. Mackenzie Olga Genilloud Ignacio Gonzlez Jos R. Tormo 《Molecules (Basel, Switzerland)》2022,27(19)
Current needs in finding new antibiotics against emerging multidrug-resistant superbugs are pushing the scientific community into coming back to Nature for the discovery of novel active structures. Recently, a survey of halophilic actinomyectes from saline substrates of El Saladar del Margen, in the Cúllar-Baza depression (Granada, Spain), led us to the isolation and identification of 108 strains from the rhizosphere of the endemic plant Limonium majus. Evaluation of the potential of these strains to produce new anti-infective agents against superbug pathogens was performed through fermentation in 10 different culture media using an OSMAC approach and assessment of the antibacterial and antifungal properties of their acetone extracts. The study allowed the isolation of two novel antibiotic compounds, kribbellichelin A (1) and B (2), along with the known metabolites sandramycin (3), coproporphyrin III (4), and kribelloside C (5) from a bioassay-guided fractionation of scaled-up active extracts of the Kribbella sp. CA-293567 strain. The structures of the new molecules were elucidated by ESI-qTOF-MS/MS, 1D and 2D NMR, and Marfey’s analysis for the determination of the absolute configuration of their amino acid residues. Compounds 1–3 and 5 were assayed against a panel of relevant antibiotic-resistant pathogenic strains and evaluated for cytotoxicity versus the human hepatoma cell line HepG2 (ATCC HB-8065). Kribbellichelins A (1) and B (2) showed antimicrobial activity versus Candida albicans ATCC-64124, weak potency against Acinetobacter baumannii MB-5973 and Pseudomonas aeruginosa MB-5919, and an atypical dose-dependent concentration profile against Aspergillus fumigatus ATCC-46645. Sandramycin (3) confirmed previously reported excellent growth inhibition activity against MRSA MB-5393 but also presented clear antifungal activity against C. albicans ATCC-64124 and A. fumigatus ATCC-46645 associated with lower cytotoxicity observed in HepG2, whereas Kribelloside C (5) displayed high antifungal activity only against A. fumigatus ATCC-46645. Herein, we describe the processes followed for the isolation, structure elucidation, and potency evaluation of these two new active compounds against a panel of human pathogens as well as, for the first time, the characterization of the antifungal activities of sandramycin (3). 相似文献