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71.
Solution polymerization of MMA, with pyridine as the solvent and BZ2O2 and AIBN as thermal initiators, was studied kinetically at 60°C. The monomer exponent varied from 0.45 to 0.91 as [BZ2O2] was increased from 1 × 10?2 to 30 × 10?2 mole/liter in a concentration range of 8.3-4.6 mole/liter for MMA. For AIBN-initiated polymerization the monomer exponent remained constant at 0.69 as [AIBN] varied from 0.4 × 10?2 to 1.0 × 10?2 mole/liter in the same concentration range for MMA. The k2p/kt Value increased in both cases with an increase in pyridine concentration in the system. This was explained in terms of an increase in the kp value, which was due presumably to the increased reactivity of the chain radicals by donor-acceptor interaction between the molecules of solvent pyridine and propagating PMMA radicals and in terms of lowering the kt value for the diffusion-controlled termination reaction due to an increase in the medium viscosity and pyridine content. 相似文献
72.
73.
Errey JC Mukhopadhyay B Kartha KP Field RA 《Chemical communications (Cambridge, England)》2004,(23):2706-2707
Enzymatic and chemo-enzymatic approaches provide straightforward access to uridine diphospho sugars irrespective of the relative and absolute configuration of the sugar, its ring size and substitution pattern. 相似文献
74.
A stochastic model is developed describing a service system subject to inhomogeneous Poisson interruptions with age dependent interruption periods. By studying the probabilistic flow of the underlying multivariate Markov process, the Laplace transform of the effective service time is explicitly obtained. For general renewal interruptions, only the expected effective service time is derived. As an application, an optimal checkpoint policy is examined for database management. It is shown that an optimal policy maximizing the ergodic availability of the database is to implement a checkpoint as soon as the cumulative uptime of the database reaches a prespecified constantk
*. A computational procedure is then developed for findingk
* and numerical results are exhibited.This work was supported in part by the National Science Foundation under Grant No. ECS-8600992 and by the IBM Program of Support for Education in the Management of Information Systems. 相似文献
75.
Fatima Flores-Galicia Alexander Eden Antoine Pallandre Sumita Pennathur Anne-Marie Haghiri-Gosnet 《Electrophoresis》2022,43(5-6):741-751
We report on the investigation of electropreconcentration phenomena in micro-/nanofluidic devices integrating 100 μm long nanochannels using 2D COMSOL simulations based on the coupled Poisson–Nernst–Planck and Navier–Stokes system of equations. Our numerical model is used to demonstrate the influence of key governing parameters such as electrolyte concentration, surface charge density, and applied axial electric field on ion concentration polarization (ICP) dynamics in our system. Under sufficiently extreme surface-charge-governed transport conditions, ICP propagation is shown to enable various transient and stationary stacking and counter-flow gradient focusing mechanisms of anionic analytes. We resolve these spatiotemporal dynamics of analytes and electrolyte ICP over disparate time and length scales, and confirm previous findings that the greatest enhancement is observed when a system is tuned for analyte focusing at the charge, excluding microchannel, nanochannel electrical double layer (EDL) interface. Moreover, we demonstrate that such tuning can readily be achieved by including additional nanochannels oriented parallel to the electric field between two microchannels, effectively increasing the overall perm-selectivity and leading to enhanced focusing at the EDL interfaces. This approach shows promise in providing added control over the extent of ICP in electrokinetic systems, particularly under circumstances in which relatively weak ICP effects are observed using only a single channel. 相似文献
76.
The present method utilizes a simple pretreatment step, cleanup on polyamide SPE cartridges, and HPLC resolution on reversed-phase C18 for the detection of the three basic nonpermitted dyes encountered in food matrixes. Polyamide cartridges were chosen because both acidic and basic dyes can be cleaned up due to their amphoteric nature. Analysis was performed on a reversed-phase C18 micro-Bondapak column using the isocratic mixture of acetonitrile-sodium acetate with a flow rate of 1.5 mL/min and a programmable lambda(max) specific visible detection to monitor colors, achieving higher sensitivity and expanded scope to test multicolor blends. All the colors showed linearity with the regression coefficient, from 0.9983 to 0.9995. The LOD and LOQ ranged between 0.107 and 0.754 mg/L and 0.371 and 2.27 mg/L or mg/kg, respectively. The intraday and interday precision gave good RSDs, and percentage recoveries in different food matrixes ranged from 75 to 96.5%. The study demonstrates that the use of a combination of a simple SPE cleanup and HPLC resolution with UV-Vis end point detection was successful in screening the presence of these three basic nonpermitted dyes individually or in blend, in a variety of food matrixes. 相似文献
77.
Kinetic and mechanistic studies of the displacement of aqua ligands from cis-[Cr(BigH)2(H2O)2]3+ (BigH = H2NC(NH)CHC(NH)NH2) by pyridine-2-aldoxime (LH) in EtOH-H2O mixtures, in the 30–45° C range, obey the following rate law over the 3.5–6.0 pH range,
相似文献
78.
I. Mukhopadhyay R. M. Lees W. Lewis-Bevan J. W. C. Johns F. Strumia G. Moruzzi 《International Journal of Infrared and Millimeter Waves》1987,8(11):1483-1502
High-resolution infrared (IR) and far infrared (FIR) Fourier transform absorption spectra have been employed to investigate assignments of FIR laser lines reported from optically-pumped13CH3OH. The spectroscopic measurements are used in conjunction with the reported IR pump and FIR laser frequencies to form closed combination loops for several systems, serving to confirm the assignments and in some cases to improve the accuracy of the FIR laser frequencies. Frequency predictions from combination differences are also presented for a number of potential new FIR laser lines. 相似文献
79.
Arsenic(III) sorption on nanostructured cerium incorporated manganese oxide (NCMO): a physical insight into the mechanistic pathway 总被引:1,自引:0,他引:1
Gupta K Bhattacharya S Nandi D Dhar A Maity A Mukhopadhyay A Chattopadhyay DJ Ray NR Sen P Ghosh UC 《Journal of colloid and interface science》2012,377(1):269-276
Arsenic(III) sorption was investigated with nanostructured cerium incorporated manganese oxide (NCMO). The pH between 6.0 and 8.0 was optimized for the arsenic(III) sorption. Kinetics and equilibrium data (pH=7.0±0.2, T=303±1.6 K, and I=0.01 M) of arsenic(III) sorption by NCMO described, respectively, the pseudo-second order and the Freundlich isotherm equations well. The sorption process was somewhat complicated in nature and divided into two different segments, initially very fast sorption followed by slow intraparticle diffusion process. Sorption reaction of arsenic(III) on NCMO was endothermic (ΔH°=+13.46 kJ mol(-1)) and spontaneous (ΔG°=-24.75 to -30.15 kJ mol(-1) at T=283-323 K), which took place with increasing entropy (ΔS°=+0.14 kJ mol(-1)K(-1)) at solid-liquid interface. Energy of arsenic(III) sorption estimated by analyzing the equilibrium data using the D-R isotherm model was 15.4 kJ mol(-1), indicating the ion-exchange type mechanism. Raman, FT-IR, pH effect, desorption, etc. studies indicated that arsenic(III) was oxidized to arsenic(V) during the sorption process. 相似文献
80.
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