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61.
We investigate the nature of the ordered phase and the orientational correlations between adjacent layers of the confined three-dimensional self-assembled rigid rod model, on the cubic lattice. We find that the ordered phase at finite temperatures becomes uniaxial in the thermodynamic limit, by contrast to the ground state (partial) order where the orientation of the uncorrelated layers is perpendicular to one of the three lattice directions. The increase of the orientational correlation between layers as the number of layers increases suggests that the unconfined model may also exhibit uniaxial ordering at finite temperatures. 相似文献
62.
A fast and sensitive method for the simultaneous determination of Sudan dyes (I, II, III, and IV) in food samples was developed for the first time using partial filling micellar electrokinectic chromatography-mass spectrometry (MEKC-MS). The use of MEKC was essential to achieve the separation of these neutral analytes, while the partial filling technique was necessary to avoid the contamination of the ion source with non-volatile micelles. MEKC separation and MS detection conditions were optimized in order to achieve a fast, efficient, and sensitive separation of the four dyes. Filling 25% of the capillary with an MEKC solution containing 40 mM ammonium bicarbonate, 25 mM SDS, and 32.5% (v/v) acetonitrile, a baseline separation of the four azo-dyes was obtained in 10 min. Tandem MS was investigated in order to improve the sensitivity and selectivity of the analysis. Limits of detection (LOD) values 5, 8, 15, and 29 times better were obtained for Sudan III, I, II, and IV, respectively, using partial filling MEKC-MS/MS instead of partial filling MEKC-MS. Under optimized conditions, LOD from 0.05 to 0.2 μg/mL were obtained. The suitability of the developed method was demonstrated through the fast and sensitive determination of Sudan I, II, III, and IV in spiked chilli powder samples. This determination could not be achieved by MEKC-UV due to the existence of several interfering compounds from the matrix. 相似文献
63.
Gisele C. X. Valle Maria I. B. Tavares Leandro Luetkmeyer Giovanni C. Stael 《Macromolecular Symposia》2007,258(1):113-118
Summary: In the last decades, the growing environmental awareness has resulted in a renewed interest in the use of natural materials for different applications. In this context, the use of wood in plastic to obtain composites has grown significantly. In the present work, heartwood and sapwood from Angelim Pedra (Hymenolobiun petraeum) were used to prepare PVC/wood composites. To study the composites with different wood types and filler contents the molecular dynamic was investigated through low field NMR by poton spin- lattice relaxation time measurements (T1H) and the thermal behavior was characterized by means of differential scanning calorimetry (DSC) focusing the glass transition temperature and thermogravimetric analyses (TGA) observing the changes in the thermal stability. It was found that increasing addition of wood flour (sapwood and heartwood) caused a small but progressive improvement of the decomposition temperature of the composites, whereas the glass transition temperature remains practically unchanged. In the molecular dynamic behavior, a gradual decrease in T1H values was observed with increasing sapwood and heartwood content, indicating that the composites became less rigid. The distribution curves of the domains showed a better interaction and phase dispersion between the composite components with higher filler content. 相似文献
64.
A. C. Tavares M. A. M. Cartaxo M.I. da Silva Pereira F. M. Costa 《Journal of Solid State Electrochemistry》2001,5(1):57-67
Studies on the electrochemical behaviour of Ni1−
x
Cu
x
Co2O4 (x ≤ 0.75) and NiCo2−
y
Cu
y
O4 (y ≤ 0.30) electrodes in 5 mol dm−3 KOH aqueous solutions are presented. The oxide layers have been prepared by thermal decomposition of aqueous nitrate solutions
on nickel supports at 623 K. Powder samples were also prepared by thermal decomposition under the same conditions. The powder
samples and the oxide layers were characterised by X-ray powder diffraction. The influence of the copper content on the voltammetric
response of the electrodes and activity towards oxygen evolution reaction is analysed and correlated with the surface composition
of the electrodes by means of X-ray photoelectron spectroscopy data. The analysis of the results reveals that the presence
of Cu affects the electrode behaviour and its influence depends on which cation has been replaced.
Received: 22 February 1999 / Accepted: 26 October 1999 相似文献
65.
M. Teresa S. R. Gomes Karina S. Tavares João A. B. P. Oliveira 《Analytical and bioanalytical chemistry》2001,369(7-8):616-619
A new sensor for calcium based on a piezoelectric quartz crystal is presented. The selectivity depends on the ratio lipophilic salt/ionophore of the composition of the coating of the quartz crystal. A crystal coated with a THF solution of PVC (34.5% w/w), DOS (62.1% w/w) and 10,19-bis[(octadecylcarbamoyl) methoxyacetyl]-1,4,7,13,16-pentaoxa-10,19-diaza cycloheneicosane (3.4% w/w) and a salt/ionophore molar proportion of 60%, corresponding to a frequency decrease of the dry crystal of 6.0 kHz, showed a detection limit to calcium of 2.2 mg/L. Both a standard calcium chloride solution and a commercially balanced salt solution for tissue culture were analyzed subsequent to ion chromatographic separation. The results obtained with the sensor developed were compared with those obtained with a conductivity detector. Although the results from both detectors agreed for the standard solution, only the quartz crystal sensor was able to give reliable results for the tissue culture solution. 相似文献
66.
In memoriam Jen? Paulik 相似文献
67.
L. C. R. Andrade M. J. M. de Almeida J. A. Paixo F. M. Fernandes Roleira E. J. Tavares da Silva 《Acta Crystallographica. Section C, Structural Chemistry》2007,63(6):o330-o331
The title compound, C21H28O4, has a 4‐acetoxy substituent positioned on the steroid α face. The six‐membered ring A assumes a conformation intermediate between 1α,2β‐half chair and 1α‐sofa. A long Csp3—Csp3 bond is observed in ring B and reproduced in quantum‐mechanical ab initio calculations of the isolated molecule using a molecular‐orbital Hartree–Fock method. Cohesion of the crystal can be attributed to van der Waals interactions and weak C—H...O hydrogen bonds. 相似文献
68.
Study of phenolic resin/EVA blends by thermal analysis 总被引:2,自引:0,他引:2
The properties of polymeric blends originate from the synergistic association of their components. In this investigation, phenolic resins obtained by the reaction of cashew-nut shell liquid (CNSL) and aldehyde are used in several applications. Mixtures of CNSL with industrial reject ethylene-co-vinyl acetate (EVA reject) were prepared with an EVA reject content up to 70%. The thermal compatibility and stability were evaluated by means of thermogravimetry (TG), derivative thermogravimetry (DTG) and differential scanning calorimetry (DSC). For blends containing a high percentage of EVA reject, the TG curves clearly show two decomposition stages, one at 350C and the other at 450C (onset 467C). The DIG curves of the blend containing 70% CNSL exhibit decomposition at 240C. The DSC curves show that the samples containing a high percentage of EVA reject are incompatible, withT
g values around –30C.The authors would like to thank PETROBRAS/CENPES/DIQUIM for the NMR facilities and thermal measurements. 相似文献
69.
A method is described for separation of impurities in uranium yellow cakes from Urgeiriça (Portugal). The trace metals are separated and concentrated by solvent extraction from 6M nitric acid into 100% TBP. The raffinate is then analysed directly by flame spectrometry. Uranium is determined gravimetrically after stripping of the organic phase. The method is fast and economic, and the results are in good agreement with those obtained by specific methods for each element after prior separation of uranium by precipitation or solvent extraction with various solvents. 相似文献
70.
Joo C. F. Nunes Raquel O. Cristvo Mara G. Freire Valria C. Santos-Ebinuma Joaquim L. Faria Cludia G. Silva Ana P. M. Tavares 《Molecules (Basel, Switzerland)》2020,25(24)
l-asparaginase (ASNase, EC 3.5.1.1) is an aminohydrolase enzyme with important uses in the therapeutic/pharmaceutical and food industries. Its main applications are as an anticancer drug, mostly for acute lymphoblastic leukaemia (ALL) treatment, and in acrylamide reduction when starch-rich foods are cooked at temperatures above 100 °C. Its use as a biosensor for asparagine in both industries has also been reported. However, there are certain challenges associated with ASNase applications. Depending on the ASNase source, the major challenges of its pharmaceutical application are the hypersensitivity reactions that it causes in ALL patients and its short half-life and fast plasma clearance in the blood system by native proteases. In addition, ASNase is generally unstable and it is a thermolabile enzyme, which also hinders its application in the food sector. These drawbacks have been overcome by the ASNase confinement in different (nano)materials through distinct techniques, such as physical adsorption, covalent attachment and entrapment. Overall, this review describes the most recent strategies reported for ASNase confinement in numerous (nano)materials, highlighting its improved properties, especially specificity, half-life enhancement and thermal and operational stability improvement, allowing its reuse, increased proteolysis resistance and immunogenicity elimination. The most recent applications of confined ASNase in nanomaterials are reviewed for the first time, simultaneously providing prospects in the described fields of application. 相似文献