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41.
L.K. Herrera S. Montalbani M. Cotte V.A. Solé A. Duran J.L. Perez-Rodriguez 《Talanta》2009,80(1):71-8428
The process of investigating paintings includes the identification of materials to solve technical and historical art questions, to aid in the deduction of the original appearance, and in the establishment of the chemical and physical conditions for adequate restoration and conservation. In particular, we have focused on the identification of several samples taken from six famous canvases painted by Pedro Atanasio Bocanegra, who created a very special collection depicting the life of San Ignacio, which is located in the church of San Justo y Pastor of Granada, Spain. The characterization of the inorganic and organic compounds of the textiles, preparation layers, and pictorial layers have been carried out using an XRD diffractometer, SEM observations, EDX spectrometry, FT-IR spectrometry (both in reflection and transmission mode), pyrolysis/gas chromatography/mass spectrometry and synchrotron-based μ-X-ray techniques. In this work, the advantages over conventional X-ray diffraction of using combined synchrotron-based μ-X-ray diffraction and μ-X-ray fluorescence in the identification of multi-layer paintings is demonstrated. 相似文献
42.
Prados-Rosales RC Herrera MC Luque-García JL de Castro L 《Journal of chromatography. A》2002,946(1-2):133-140
A fast microwave-assisted dansylation procedure has been developed for the derivatization of N-nitrosamines prior to high-performance liquid chromatography determination. N-Nitrosomorpholine, N-nitrosodimethylamine, N-nitrosodiethylamine, N-nitrosopyrrolidine and N-nitrosopiperidine are first denitrosated by hydrobromic acid-acetic acid to produce secondary amines, which are then quantitatively dansylated in 5 min using radiation power of 378 W and a maximum pressure of 1.4 bar inside the reactor. The reaction mixture is separated on a C18 column with acetonitrile-water (55:45, v/v) as mobile phase with fluorimetric detection at 531 nm (excitation at 339 nm). The detection limits range from 8 to 75 pg for N-nitrosomorpholine and N-nitrosodiethylamine, respectively. The method was applied to study the recoveries of N-nitrosamines in beer and their determination in cigarette smoke. 相似文献
43.
44.
Cuadra P Herrera R Fajardo V 《Journal of photochemistry and photobiology. B, Biology》2004,76(1-3):61-68
Treatment of Jaborosa magellanica with artificial UV-B radiation caused changes in plant growth, plant chemistry and increase DNA polymorphisms. Spectrophotometric analysis showed that UV-B radiation decreases the chlorophylls content, and increases the amount of UV-B absorbing compounds (e.g., phenylpropanoids). Other UV-induced alterations include reduction in leaf area, alterations in plant architecture, and DNA damage. Using random primers and PCR amplification procedure, a high degree of polymorphism was detected when treated plants were compared to non-irradiated plants. These biochemical changes may be interpreted as plant response to UV-B radiation stress and as an indicator of DNA damage. 相似文献
45.
J. M. Hernndez Ana M. Herrera J. García‐Serrano J. F. Rivas‐Silva 《International journal of quantum chemistry》2002,88(3):342-346
Conformations of p‐methacryloylaminophenylarsonic acid (p‐MAPHA) are determined through molecular mechanics and DFT/B3LYP calculations. Solvation effects are studied within the self‐consistent isodensity continuum model (SCI‐PCM). The stationary points were found to correspond to minima as verified by the analysis of vibrational frequencies in the molecule. The molecular optical absorption was obtained by using different solvent environments. The present results are in good agreement with the available experimental data. © 2002 Wiley Periodicals, Inc. Int J Quantum Chem, 2002 相似文献
46.
Investigation of pyrolysis of chinese coals using thermal analysis/mass spectrometry 总被引:2,自引:0,他引:2
Li X. Matuschek G. Herrera M. Wang H. Kettrup A. 《Journal of Thermal Analysis and Calorimetry》2003,71(2):601-612
TA/MS (thermal analysis coupled with mass spectrometry) was applied to the pyrolysis of Chinese coals with different ranks.
A total of 13 Chinese coals were investigated. The samples were deliberately chosen to represent the 13 types of Chinese coals
according to the Chinese coal classification system. The experiments were carried out in an argon atmosphere with a flow rate
of 150 ml min-1. The samples were heated from 40 up to 1200°C with a constant heating rate of 10 k min-1. The main evolved pyrolysis products were identified through the on-line recorded mass spectra. The thermal and evolution
behavior was compared between the coals. The results showed a strong thermal and evaluation behavior dependence on the coal
rank. Different aliphatic fragments and also some aromatic substances, which are of environmental concern (BTX, PAHs), were
found to be released depending on the different types of coal.
This revised version was published online in July 2006 with corrections to the Cover Date. 相似文献
47.
Vladimir A Escobar Barrios Alain Petit Rafael Herrera Nájera 《European Polymer Journal》2003,39(6):1151-1167
Three types of butadiene-styrene copolymers, diblock, triblock and random, were partially hydrogenated in their elastomeric units in order to determine the influence of hydrogenation extent on their thermal properties. The hydrogenation reactions were carried out using a Ziegler-Natta type catalyst and the extent of hydrogenation was evaluated by FTIR spectroscopic technique. The percentage of crystallinity was determined by differential scanning calorimetry (DSC), considering the low density polyethylene (LDPE) as reference since the saturation of elastomeric units with low content of 1,2-vinyl bonds gives a structure which resembles to LDPE, thus semi-crystalline polymers were obtained. On the other hand, the glass transition temperature (Tg) for the hydrogenated and non-hydrogenated copolymers as well as their heat of fusion, were also determined by DSC. An equation to evaluate the Tg of partially hydrogenated random copolymers is proposed considering both the saturated and unsaturated fractions. The thermo-oxidative behaviour of certain hydrogenated and non-hydrogenated copolymers was evaluated by thermogravimetric analyses (TGA). The results obtained by TGA suggest that a minimum saturation level is necessary in order to improve the thermo-oxidative resistance of the polymers. 相似文献
48.
Determination of estrogens in environmental water samples using 1,3‐dipentylimidazolium hexafluorophosphate ionic liquid as extraction solvent in dispersive liquid–liquid microextraction 下载免费PDF全文
Bárbara Socas‐Rodríguez Javier Hernández‐Borges María Asensio‐Ramos Antonio V. Herrera‐Herrera Jose A. Palenzuela Miguel Ángel Rodríguez‐Delgado 《Electrophoresis》2014,35(17):2479-2487
In this work, the potential of a symmetric dialkyl‐substituted ionic liquid (IL), 1,3‐dipenthylimidazolium hexafluorophosphate ([PPIm][PF6]), as extraction solvent in dispersive liquid–liquid microextraction (DLLME) has been studied for the analysis of a group of three natural (estriol, 17β‐estradiol, and 17α‐estradiol) and four synthetic (17α‐ethynylestradiol, diethylstibestrol, dienestrol, and hexestrol) estrogenic compounds as well as one mycotoxin with estrogenic activity (zearalenone) in different types of water samples (Milli‐Q, mineral, and wastewater). Separation, determination, and quantification were developed by HPLC‐DAD and a fluorescence detector (FD) connected in series. Factors influencing the IL‐DLLME procedure (sample pH, amount of IL, type and volume of disperser solvent, ionic strength, and assistance of vortex agitation) were investigated and optimized by means of a step‐by‐step approach. Once the optimum extraction conditions were established (10 mL of water at pH 8, 60 mg of [PPIm][PF6], 500 μL of ACN as disperser solvent and vortex agitation for 1 min), the calibration curves of the whole method (IL‐DLLME‐HPLC‐DAD/FD) were obtained and precision and accuracy were evaluated. It was demonstrated that the developed methodology was repeatable, accurate, and selective with limits of detection in the 0.30–0.57 μg/L and 13.8–37.1 μg/L range for FD and DAD, respectively. Relative recovery values were higher than 85% for the different types of water samples and the Student's t test demonstrated that there were not significant differences between the added and the found concentration. 相似文献
49.
Influence of substrate temperature and N2/Ar flow ratio on the stoichiometry,structure and hardness of TaNx coatings deposited by DC reactive sputtering 下载免费PDF全文
K. Valdez D. G. Espinosa‐Arbeláez J. E. García‐Herrera J. Muñoz‐Saldaña M. H. Farias W. De la Cruz 《Surface and interface analysis : SIA》2015,47(11):1015-1019
The effect of substrate temperature and N2/Ar flow ratio on the stoichiometry, structure and hardness of TaNx coatings prepared on (111) Si substrates by DC reactive sputtering was investigated. For the structural, chemical and morphological analysis, X‐ray diffraction (XRD), Auger electron scanning and atomic force microscopy were respectively used. Hardness values of thin films were determined using the work of indentation model from nanoindentation measurements. TaN stoichiometric coatings were obtained for samples deposited at room temperature. The stoichiometric TaN phase was not obtained by increasing the temperature up to 773 K, even when increasing the N2/Ar flow ratio. Even when a saturation in nitrogen content was achieved, nitrogen vacancies are still present in those samples. For coatings prepared at 773 K and low N2/Ar flow ratio, a phase mixture between TaNx and cubic α‐Ta was observed, while a cubic structure δ‐TaN was formed by increasing the N2/Ar flow ratio. A maximum in hardness and (38 GPa) was obtained for the sample deposited at 773 K and a N2/Ar flow ratio of 0.2, which presented a δ‐TaN cubic crystalline structure and a roughness value of 1.6 nm. Copyright © 2015 John Wiley & Sons, Ltd. 相似文献
50.
Asymmetric Synthesis of Fluorinated Isoindolinones through Palladium‐Catalyzed Carbonylative Amination of Enantioenriched Benzylic Carbamates 下载免费PDF全文
Dr. Pablo Barrio Ignacio Ibáñez Lidia Herrera Dr. Raquel Román Dr. Silvia Catalán Prof. Dr. Santos Fustero 《Chemistry (Weinheim an der Bergstrasse, Germany)》2015,21(32):11579-11584
The asymmetric synthesis of fluorinated isoindolinones has been achieved by a palladium‐catalyzed aminocarbonylation reaction of the corresponding α‐fluoroalkyl o‐iodobenzylamines. A base‐mediated anti β‐hydride elimination process was suggested to explain the partial erosion of the optical purity observed in some cases. This mechanistic rationale enabled the minimization of this partial racemization by fine‐tuning the pKa of the base. 相似文献