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21.
Taha M. Abdel-Rahman 《Phosphorus, sulfur, and silicon and the related elements》2013,188(8):1737-1754
A novel method for the synthesis of 1,3,4-thiadiazole and 1,3,4-thiadiazine derivatives bearing a carbazole moiety is described. Carbazole was transformed into carbazole-9-thiocarbohydrazide in two steps. This compound was allowed to react with various electrophiles to yield 1,3,4-thiadiazole derivatives. The reaction with bifunctional electrophiles led to 1,3,4-thiadiazines. 2-(Carbazol-9-yl)-5,6-dihydro-4H-1,3,4-thiadiazin-5-one reacted with piperidine and formaldehyde to yield the 4-(piperidin-1-ylmethyl) derivative. The reaction with aromatic aldehydes led to the corresponding 6-arylidene derivatives, which were transformed into pyrimidino[4,5-e]-1,3,4-thiadiazines and pyrazolo[3,4-e]-1,3,4-thiadiazines by a reaction with guanidine, acetamidine, or phenylhydrazine, respectively. Structures of the products were confirmed by 1H NMR, 13C NMR, IR, and mass spectrometric measurements. Selected examples of products were screened for anticancer activity. 相似文献
22.
M. M. Ghorab N. E. Amin M. S. A. El Gaby N. M. H. Taha M. A. Shehab I. M. I. Faker 《Phosphorus, sulfur, and silicon and the related elements》2013,188(12):2918-2928
The key intermediate diisothiocyanate 2 was allowed to react with 5-amino-3-methyl-pyrazole-4-carbonitrile 3, ethyl 5-amino-1-phenyl-pyrazole-4-carboxylate 6, 2-amino-tetrahydrobenzo[b]thiophene-3-car-bonitrile 9, ethyl-2-amino-tetra-hydrobenzo[b]thiophene-3-carboxylate 12, and/or 1,2,4-triazole 15 to give the corresponding biscompounds 4, 5, 7, 8, 10, 11, 13, 14, and 16, respectively. The structure of the synthesized compounds was elucidated by elemental analyses and spectral data. Some of the prepared compounds were tested for their antimicrobial and antitumor activities. 相似文献
23.
The complexation equilibria of Fe(III) with two buffer families, which are ubiquitous in biological system studies, were studied by potentiometric measurements at a constant ionic strength of I = 0.1 mol·dm?3 NaNO3 in aqueous solutions at 298.15 K. The members of TRIS family are tris(hydroxymethyl)aminomethane (TRIS), N-[tris(hydroxymethyl)methyl]-2-aminoethanesulfonic acid (TES), N-[tris(hydroxymethyl)methyl]-3-aminopropanesulfonic acid (TAPS), N-[tris(hydroxymethyl)methyl]-3-amino-2-hydroxypropanesulfonic acid (TAPSO), and N-tris(hydroxymethyl)methyl-4-aminobutanesulfonic acid (TABS) buffers. The members of morpholine family are 4-morpholineethanesulfonic acid (MES), 4-morpholinepropanesulfonic acid (MOPS), 3-morpholino-2-hydroxypropanesulfonic acid (MOPSO), and 4-(N-morpholino) butanesulfonic acid (MOBS) buffers. The overall stability constants were determined from pH-metric data using the least-squares curve-fitting program HYPERQUAD 2008. Based on the best-fit results, the species formed at equilibrium are ML, ML2, ML2H?1, and ML3 in the systems with TRIS family buffers. The complex species ML, ML2, ML2H?1, and MLH?1 are formed in the MOPSO-containing system, while ML, ML2, and ML2H?1 are formed in the systems with MES, MOPS, and MOBS. The stabilities of the complexes fall in the order TABS > TRIS > TAPS > TAPSO > TES and MOBS > MOPS > MOPSO > MES for the TRIS family and morpholine families, respectively. 相似文献
24.
The present work deals with uranium removal from a nitric acid raffinate (waste) solution using prepared solvent (tri-butyl phosphate, TBP) immobilizing PVC cement (SIC) as a suitable adsorbent. The studied relevant factors affecting uranium adsorption onto SIC adsorbent involved; contact time, solution molarity, initial uranium concentration and temperature. The obtained adsorption isotherm of uranium onto the SIC adsorbent was fitted to Langmuir, Freundlich and Dubinin–Radushkviech (D–R) adsorption models. The results showed that the obtained equilibrium data fitted well the Langmuir isotherm. Additionally, it was found that the adsorption process obeys the pseudo second-order kinetic model. On the other hand, the calculated theoretical capacity of our prepared SIC adsorbent reached about 17 g U/kg SIC. Uranium adsorption from the studied raffinate solution was carried out applying the attained optimum conditions. The obtained data showed that 58.4 mg U/5 g SIC were adsorbed. However, using of 2 M HNO3 solution as an eluent, 93 (54.3 mg U) from the adsorbed amount were eluted. 相似文献
25.
Mohamed H. Taha Samir A. Abdel Maksoud Mohsen M. Ali Ahmed M. A. El Naggar Asmaa S. Morshedy Amir A. Elzoghby 《International journal of environmental analytical chemistry》2013,93(12):1211-1234
ABSTRACTThis study reports the removal of organic matters from phosphoric acid using waste-produced bio-charcoal structures. Particularly, the freshly made bio-char species via pyrolysis and two sub-driven acids activated charcoals were applied during the removal process. The treated charcoal with hydrochloric and nitric acids had attained a higher adsorption rate for organic matters than that of the non-treated one. Removal percentages of 70% and 60% were, respectively, attained by acid-modified chars. The kinetics of the adsorption process was fitted via pseudo-first/second-order and Morris–Weber models. The thermodynamic parameters of the presented sorption process indicate that organic matter removal has been endothermic, physical and spontaneous. 相似文献
26.
Dielectric spectra of CPVC stabilized with cyanoguanidine were studied in the temperature range 300–450 K and frequency range 10 kHz to 1 MHz. In these conditions, only one clear dielectric relaxation band (α-type) associated with dipolar polarization was observed. Dielectric losses was found to directly proportional to the number of dipoles (N) which reflects the orientational distribution of polymer chains in the amorphous region, at which dielectric losses concerned. Calculations of the dielectric modulus M′(T) at low temperature indicate that there is a role of the electrode polarization in the relaxation process. Dielectric loss data were used to calculate the activation enthalpy by two different methods, the obtained value was 450 kJ/mol. 相似文献
27.
The degradation of the nearby generation of high‐density polyethylene (HDPE) loaded with 2.5% of carbon black (CB) content (ie, HDPE/CB composites) is studied experimentally with the end goal of radiation safety applications. The impact of various γ‐irradiation doses in the air on the nanostructure of free volume and durability has been researched. The free volume was evaluated utilizing the positron annihilation lifetime (PAL) technique while the durability was contemplated by measuring the mechanical properties such as strain, elongation at break, and tear resistance. The electrical conductivity was explored to demonstrate the impact of the irradiation dose on the conductivity of the samples. Surface morphology studies using a scanning electron microscope (SEM) showed the surface fracture of HDPE/CB composites for unirradiated and irradiated samples. The surface roughness of the HDPE/CB GMs increases with increasing the irradiation dose. Among various uses of HDPE/CB composites, sheets are liners of dumps used to dispose of interim storage for Low and Medium Level Waste of NORMs and TENORMs. HDPE Geomembrane liners proved its utilization from the results of present research of electrical, mechanical tests, and SEM morphology to have the required resistance to weather conditions. 相似文献
28.
A complete infrared study of the mixed crystal system of AgNO3 and NaNO3 is carried out in the region 400–4000 cm?1. The study includes internal fundamental normal vibrations of the NO?3 ion in the ordered and disordered phases of AgNO3 at different values of the sodium concentration, the I.R. spectra, spectral band shape intensities, and frequencies of the internal modes as functions of the sodium ion concentration. Special attention is paid to bending mode, combination mode, asymmetric stretching mode, and over-tone. The rotational energy barrier is determined at different concentrations of the sodium ions in the system. 相似文献
29.
The reversible phase transformation of AgNO3 is studied. Dielectric constant, d.c. resistivity, differential thermal analysis (DTA) and dilatometric measurements show the occurrence of a reversible phase transition II→I at 160°C with heat of transformation H = 0.78 kcal/mol. The thermal hysteresis in this reversible transformation is examined, the magnitude of the temperature hysteresis does not exceed 12°C. An acceptable agreement is observed between the measured values of the transition temperature obtained by three different experimental techniques. The dilatometric analysis shows that this transition is accompanied by thermal shrinkage with relative shrinkage coefficient 8 × 10?4. Thermal analysis are also used to get thermodynamic and kinetic data of this phase transition. The temperature dependence of the dielectric constant and d.c. resistivity for single crystals as well as polycrystalline samples of AgNO3 have clearly located and confirm the phase transitions II→I→II with a strong support to its thermal hysteresis character. The conduction mechanism is found to be activated by energy 0.12 eV for phase I and 0.36 eV for phase II. The observed thermal behaviour of the various measured parameters is attributed to orientational disorder of the nitrate group leading to an order-disorder phase transition which is reported here for first time in AgNO3. 相似文献
30.
Taha Sochi 《Transport in Porous Media》2010,85(2):489-503
Yield-stress is a problematic and controversial non-Newtonian flow phenomenon. In this article, we investigate the flow of
yield-stress substances through porous media within the framework of pore-scale network modelling. We also investigate the
validity of the Minimum Threshold Path (MTP) algorithms to predict the pressure yield point of a network depicting random
or regular porous media. Percolation theory as a basis for predicting the yield point of a network is briefly presented and
assessed. In the course of this study, a yield-stress flow simulation model alongside several numerical algorithms related
to yield-stress in porous media were developed, implemented and assessed. The general conclusion is that modelling the flow
of yield-stress fluids in porous media is too difficult and problematic. More fundamental modelling strategies are required
to tackle this problem in the future. 相似文献