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781.
Desloge JG Reed CM Braida LD Perez ZD Delhorne LA 《The Journal of the Acoustical Society of America》2011,129(6):3884-3896
A functional simulation of hearing loss was evaluated in its ability to reproduce the temporal modulation transfer functions (TMTFs) for nine listeners with mild to profound sensorineural hearing loss. Each hearing loss was simulated in a group of three age-matched normal-hearing listeners through spectrally shaped masking noise or a combination of masking noise and multiband expansion. TMTFs were measured for both groups of listeners using a broadband noise carrier as a function of modulation rate in the range 2 to 1024 Hz. The TMTFs were fit with a lowpass filter function that provided estimates of overall modulation-depth sensitivity and modulation cutoff frequency. Although the simulations were capable of accurately reproducing the threshold elevations of the hearing-impaired listeners, they were not successful in reproducing the TMTFs. On average, the simulations resulted in lower sensitivity and higher cutoff frequency than were observed in the TMTFs of the hearing-impaired listeners. Discrepancies in performance between listeners with real and simulated hearing loss are possibly related to inaccuracies in the simulation of recruitment. 相似文献
782.
The micro cutting process of microstructured material is simulated with consideration of the heterogeneities of the microstructure. In the case of cp-titanium with its hcp crystal structure the basal and prismatic slip systems are taken into account. The concept of crystal plasticity for large deformations is applied considering elastic anisotropy, self and latent hardening. The visco-plastic evolution law incorporates rate dependent material behavior. This setup is implemented within the finite element method. The effects of the microstructure are demonstrated by an illustrative example and a comparison to an isotropic von Mises elasto-plastic material. (© 2015 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim) 相似文献
783.
784.
Young Pyo Hong Sophie‐Charlotte Gleber Thomas V. O'Halloran Emily L. Que Reiner Bleher Stefan Vogt Teresa K. Woodruff Chris Jacobsen 《Journal of synchrotron radiation》2014,21(1):229-234
X‐ray fluorescence nanotomography provides unprecedented sensitivity for studies of trace metal distributions in whole biological cells. Dose fractionation, in which one acquires very low dose individual projections and then obtains high statistics reconstructions as signal from a voxel is brought together (Hegerl & Hoppe, 1976), requires accurate alignment of these individual projections so as to correct for rotation stage runout. It is shown here that differential phase contrast at 10.2 keV beam energy offers the potential for accurate cross‐correlation alignment of successive projections, by demonstrating that successive low dose, 3 ms per pixel, images acquired at the same specimen position and rotation angle have a narrower and smoother cross‐correlation function (1.5 pixels FWHM at 300 nm pixel size) than that obtained from zinc fluorescence images (25 pixels FWHM). The differential phase contrast alignment resolution is thus well below the 700 nm × 500 nm beam spot size used in this demonstration, so that dose fractionation should be possible for reduced‐dose, more rapidly acquired, fluorescence nanotomography experiments. 相似文献
785.
Configurational forces can be interpreted as driving forces on material inhomogeneities such as crack tips. In dissipative media the total configurational force on an inhomogeneity consists of an elastic contribution and a contribution due to the dissipative processes in the material. For the computation of discrete configurational forces acting at the nodes of a finite element mesh, the elastic and dissipative contributions must be evaluated at integration point level. While the evaluation of the elastic contribution is straightforward, the evaluation of the dissipative part is faced with certain difficulties. This is because gradients of internal variables are necessary in order to compute the dissipative part of the configurational force. For the sake of efficiency, these internal variables are usually treated as local history data at integration point level in finite element (FE) implementations. Thus, the history data needs to be projected to the nodes of the FE mesh in order to compute the gradients by means of shape function interpolations of nodal data as it is standard practice. However, this is a rather cumbersome method which does not easily integrate into standard finite element frameworks. An alternative approach which facilitates the computation of gradients of local history data is investigated in this work. This approach is based on the definition of subelements within the elements of the FE mesh and allows for a straightforward integration of the configurational force computation into standard finite element software. The suitability and the numerical accuracy of different projection approaches and the subelement technique are discussed and analyzed exemplarily within the context of a crystal plasticity model. (© 2014 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim) 相似文献
786.
787.
Simultaneous detection of stable isotope‐labeled and unlabeled l‐tryptophan and of its main metabolites,l‐kynurenine,serotonin and quinolinic acid,by gas chromatography/negative ion chemical ionization mass spectrometry
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Mitsue Sano Véronique Ferchaud‐Roucher Charlotte Nael Audrey Aguesse Guillaume Poupeau Blandine Castellano Dominique Darmaun 《Journal of mass spectrometry : JMS》2014,49(2):128-135
A method for the detection of unlabeled and 15N2‐labeled l ‐tryptophan (l ‐Trp), l ‐kynurenine (l ‐Kyn), serotonin (5‐HT) and quinolinic acid (QA) in human and rat plasma by GC/MS is described. Labeled and unlabeled versions of these four products were analyzed as their acyl substitution derivatives using pentafluoropropionic anhydride and 2,2,3,3,3‐pentafluoro‐1‐propanol. Products were then separated by GC and analyzed by selected ion monitoring using negative ion chemical ionization mass spectrometry. l ‐[13C11, 15N2]‐Trp, methyl‐serotonin and 3,5‐pyridinedicarboxylic acid were used as internal standards for this method. The coefficients of variation for inter‐assay repeatability were found to be approximately 5.2% for l ‐Trp and 15N2‐Trp, 17.1% for l ‐Kyn, 16.9% for 5‐HT and 5.8% for QA (n = 2). We used this method to determine isotope enrichments in plasma l ‐Trp over the course of a continuous, intravenous infusion of l ‐[15N2]Trp in pregnant rat in the fasting state. Plasma 15N2‐Trp enrichment reached a plateau at 120 min. The free Trp appearance rate (Ra) into plasma was 49.5 ± 3.35 µmol/kg/h. The GC/MS method was applied to determine the enrichment of 15N‐labeled l ‐Trp, l ‐Kyn, 5‐HT and QA concurrently with the concentration of non‐labeled l ‐Trp, l ‐Kyn, 5‐HT and QA in plasma. This method may help improve our understanding on l ‐Trp metabolism in vivo in animals and humans and potentially reveal the relative contribution of the four pathways of l ‐Trp metabolism. Copyright © 2014 John Wiley & Sons, Ltd. 相似文献
788.
Hind El Hadri Julien Gigault Philippe Chéry Martine Potin-Gautier Gaëtane Lespes 《Analytical and bioanalytical chemistry》2014,406(6):1639-1649
The methodological approach used to robustly optimize the characterization of the polydisperse colloidal phase of drain water samples is presented. The approach is based on asymmetric flow field-flow fractionation coupled to online ultraviolet/visible spectrophotometry, multi-angle light scattering, and inductively coupled plasma mass spectrometry. Operating factors such as the amount of sample injected and the ratio between main-flow and cross-flow rates were considered. The evaluation of the injection and fractionation steps was performed considering the polydispersity index and the contribution to the polydispersity of the plate height, the recovery, the retention ratio and the size range of the fractionated colloids. This approach allows the polydispersity of natural colloid samples to be taken into consideration to achieve the most efficient and representative fractionation. In addition to the size characterization, elemental analysis was also evaluated using the recovery, precision, and limits of detection and quantification relative to a trace element of interest (copper) in drain water. To complete this investigation, the potential application of the methodology was assessed using several independent drain water samples from different soils. The contribution of the polydispersity to the plate height ranges from 4.8 to 8.9 cm with a mean precision of 6 %. The mean colloidal recovery was 81?±?3 %, and the mean retention ratio was 0.043–0.062. The limits of detection and quantification for copper were 0.6 and 1.8 μg L?1, respectively. 相似文献
789.
Petra Slabizki Charlotte Legrum Reinhard Meusinger Hans-Georg Schmarr 《Analytical and bioanalytical chemistry》2014,406(25):6429-6439
The three constitutional isomers of dimethyl-substituted methoxypyrazines: 3,5-dimethyl-2-methoxypyrazine 1; 2,5-dimethyl-3-methoxypyrazine 2; and 2,3-dimethyl-5-methoxypyrazine 3 are potent flavor compounds with similar mass spectrometric, gas chromatographic, and nuclear magnetic resonance spectroscopic behavior. Therefore, unambiguous analytical determination is critical, particularly in complex matrices. The unequivocal identification of 1–3 could be achieved by homo- and heteronuclear NMR correlation experiments. The observed mass fragmentation for 1–3 is proposed and discussed, benefitting from synthesized partially deuterated 1 and 2. On common polar and apolar stationary phases used in gas chromatography (GC) 1 and 2 show similar behavior whereas 3 can be separated. In our focus on off-flavor analysis with respect to wine aroma, 1 has been described as a “moldy” off-flavor compound in cork and 2 as a constituent in Harmonia axyridis contributing to the so-called “ladybug taint,” whereas 3 has not yet been described as a constituent of wine aroma. A successful separation of 1 and 2 could be achieved on octakis-(2,3-di-O-pentyl-6-O-methyl)-γ-cyclodextrin as stationary phase in GC. Applying heart-cut multidimensional GC analysis with tandem mass spectrometric detection we could confirm the presence of 1 as a “moldy” off-flavor compound in cork. However, in the case of Harmonia axyridis, a previous identification of 2 has to be reconsidered. In our experiments we identified the constitutional isomer 1, which was also found in Coccinella septempunctata, another species discussed with respect to the “ladybug taint.” The analysis of such structurally related compounds is a demonstrative example for the importance of a chromatographic separation, as mass spectrometric data by itself could not guarantee the unequivocal identification. 相似文献
790.
Functionalized Carbon Nanoparticles,Blacks and Soots as Electron‐Transfer Building Blocks and Conduits
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Dr. Katherine Lawrence Charlotte L. Baker Prof. Tony D. James Dr. Steven D. Bull Dr. Ruth Lawrence Dr. John M. Mitchels Prof. Marcin Opallo Prof. Omotayo A. Arotiba Prof. Kenneth I. Ozoemena Prof. Frank Marken 《化学:亚洲杂志》2014,9(5):1226-1241
Functionalized carbon nanoparticles (or blacks) have promise as novel active high‐surface‐area electrode materials, as conduits for electrons to enzymes or connections through lipid films, or as nano‐building blocks in electroanalysis. With previous applications of bare nanoblacks and composites mainly in electrochemical charge storage and as substrates in fuel cell devices, the full range of benefits of bare and functionalized carbon nanoparticles in assemblies and composite (bio)electrodes is still emerging. Carbon nanoparticles are readily surface‐modified, functionalized, embedded, or assembled into nanostructures, employed in bioelectrochemical systems, and incorporated into novel electrochemical sensing devices. This focus review summarizes aspects of a rapidly growing field and some of the recent developments in carbon nanoparticle functionalization with potential applications in (bio)electrochemical, photoelectrochemical, and electroanalytical processes. 相似文献