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871.
The reaction between the thionine (Th) and the ribose was observed spectrophotometrically and changes in absorbance of Th were recorded at variable concentration of dye, reductant and pH. A pseudo first order rate of reaction was found to establish the reduction kinetics of the dye, studied at a pH range of 0.34 to 12.8. Absorption spectrum of Th at different pH, with ribose showed a pH (12.8) dependent introversion. The reduction most probably took place with enediol intermediate of the sugar at high pH. A full geometry optimization of predominant species of Th namely, mono‐deprotonated, di‐deprotonated Th, and LTh (leuco thionine) respectively, at low and high pH, was performed at B3LYP level of theory. The data obtained from the energy minimization were in excellent agreement with other experimental and theoretical observations. The calculated enthalpies of formation for both reduction reactions (mono‐deprotonated Th+H+→leucothionine and di‐deprotonated Th+2H+→leucothionine) provided evidences for maximum reduction of the dye at high pH. 相似文献
872.
Albahily K Fomitcheva V Gambarotta S Korobkov I Murugesu M Gorelsky SI 《Journal of the American Chemical Society》2011,133(16):6380-6387
Reaction of the divalent [(t-Bu)NP(Ph)(2)N(t-Bu)]CrCl(2)Li(THF)(2) (1) with 1 equiv of vinyl Grignard (CH(2)=CH)MgCl reproducibly afforded the triangulo {π-[(t-Bu)N-P(Ph)(2)-N(t-Bu)]Cr}(2)(μ,μ',η(4),η(4)'-C(4)H(4)){σ-[(t-Bu)N-P(Ph)(2)-N(t-Bu)]Cr} (2) containing a σ-/π-bonded butadiene-diyl unit. The diene-diyl moiety was generated by an oxidative coupling and deprotonation of two vinyl anions. The crystal structure revealed that of the three chromium atoms, each bearing one NPN ligand, two are perpendicularly bonded to the two sides of the π-system of the butadiene-diyl residue in a sort of inverted sandwich type of structure. The third is instead coplanar with the doubly deprotonated C(4) unit and σ-bonded to the two terminal carbon atoms. Despite the appearance as a Cr(II)/Cr(I) mixed valence species, DFT calculations have revealed that the structure of 2 consists of three divalent chromium atoms, while the additional electron resides on the π-system of the bridging organic residue. Complex 2 behaves as a single component selective catalyst for ethylene trimerization. 相似文献
873.
The blood glucose monitoring devices (BGMDs) are an integral part of diabetes management now-a-days. They have evolved tremendously within the last four decades in terms of miniaturization, rapid response, greater specificity, simplicity, minute sample requirement, painless sample uptake, sophisticated software and data management. This article aims to review the developments in the technologies behind commercial BGMD, especially those in the areas of chemistries, mediators and other components. The technology concerns, on-going developments and future trends in blood glucose monitoring (BGM) are also discussed. 相似文献
874.
Adamou R Coly A Abdoulaye A Soumaila M Moussa I Ikhiri K Tine A 《Journal of fluorescence》2011,21(4):1409-1415
An analytical method based on the use of UV-irradiation to produce fluorescent derivatives from Etofenprox a non-fluorescent
pyrethroid insecticide is described. The impact of cetyltrimethylammonium chloride (CTAC) micellar medium on the Etofenprox
photochemically-induced fluorescence (PIF) is reported. Parameters influencing the sensitivity and repeatability of the PIF
method have been optimized. The alkaline medium (NaOH 6 × 10−2 M) + CTAC surfactant molecules (3.84 mg/ml) in acetonitrile is found to be very suitable for this pyrethroid insecticide
analysis in environment matrices. Linear dynamic range is established over more than two orders of magnitude. The limit of
detection is lower than 5 ng/ml. The method seems to be suitable for environmental matrices quality control. Application to
the analysis of spiked natural waters gave recoveries rate ranged from 94 to 104% and 107 to 115% respectively for river and
pound water. 相似文献
875.
Muhammad Tariq Saeed Chani Kh. S. Karimov F. A. Khalid S. Z. Abbas M. B. Bhatty 《中国物理 B》2013,22(1):10701-010701
This study presents the fabrication and investigation of humidity sensors based on orange dye (OD) and polyaniline (PANI) composite films. A blend of 3 wt.% OD with 1 wt.% PANI was prepared in 1 ml water. The composite films were deposited on glass substrates between pre-deposited silver electrodes. The gap between the electrodes was 45 μm. The sensing mechanism was based on the impedance and capacitance variations due to the absorption/desorption of water vapor. It was observed that with the increase in relative humidity (RH) from 30% to 90%, the impedance decreases by 5.2 × 10 4 and 8.8 × 10 3 times for the frequencies of 120 Hz and 1 kHz, respectively. The impedance-humidity relationship showed a more uniform change compared to the capacitance-humidity relationship in the RH range of 30% to 90%. The consequence of annealing, measuring frequency, response and recovery time, and absorption-desorption behavior of the humidity sensor were also discussed in detail. The annealing resulted in an increase in sensitivity of up to 2.5 times, while the measured response time and recovery time were 34 s and 450 s, respectively. The impedance-humidity relationship was simulated. 相似文献
876.
Hongwei Ge Kui Zhang Huan Yu Ji Yue Long Yu Xinfeng Chen Tianxin Hou Khalid A. Alamry Hadi M. Marwani Suhua Wang 《Journal of fluorescence》2018,28(6):1405-1412
This paper reported a dual-mode probe for D-penicillamine on the basis of pH-mediated gold nanoparticles aggregation and fluorescence resonance energy transfer (FRET) from carbon dots. D-penicillamine is a zwitterionic compound and has different forms depending on specific pH ranges. The thiol group of D-penicillamine has high affinity towards the surface of gold nanoparticles and can replace other surface ligands. When pH values were close to its isoelectrical point (pH(I)), the D-penicillamine capped gold nanoparticles aggregated through hydrogen bonding or electrostatic interactions, resulting in the releasing of carbon dots from gold nanoparticles. The dual-mode probe consisted of fluorescent carbon dots and gold nanoparticles, and the fluorescence of carbon dots was quenched by the attached gold nanoparticles due to the FRET. Then, the fluorescence can be recovered in presence of D-penicillamine due to the gold nanoparticles aggregation in specific pH range. Under the optimum conditions, the probe has linear response for D-penicillamine in the 0.25–1.5 μM concentration range with a detection limit of 0.085 μM. This method provides a potential application in sensitive detection of D-penicillamine. 相似文献
877.
878.
Yu Xia Khalid Hadi Genya Hashimoto Nozomu Hashimoto Osamu Fujita 《Proceedings of the Combustion Institute》2021,38(3):4043-4052
Because ammonia is one of the most promising candidates for energy carrier in the future, various applications of ammonia as a fuel are currently considered. One medium for utilizing ammonia is by introducing it to coal-fired boilers. To the best of our knowledge, this paper is the first to report the fundamental mechanism of the flame propagation phenomenon for pulverized coal/ammonia co-combustion. The effects of the equivalence ratio of the ammonia-oxidizer mixture on the flame propagation velocity of pulverized coal/ammonia co-combustion in turbulent fields were clarified by the experiments employing a unique fan-stirred constant volume chamber. The flame propagation velocities of pulverized coal/ammonia co-combustion, pure ammonia combustion, and pure pulverized coal combustion were compared. As expected, the flame propagation velocity of pulverized coal/ammonia was higher than that of the pure pulverized coal combustion for all conditions. However, the comparison of the flame propagation velocities of pulverized coal/ammonia co-combustion and that of the pure ammonia combustion, revealed that whether the flame propagation of the pulverized coal/ammonia was higher than that of the pure ammonia combustion was dependent on the equivalence ratio of the ammonia-oxidizer. This unique feature was explained by a mechanism including three competing effects proposed by the authors. In the ammonia lean condition, the positive effects, which are the strong radiation from the luminous flame and the increment of local equivalence ratio by the addition of volatile matter, are larger than the negative effect, which is the heat absorption by coal particles in preheat zone. In the ammonia rich condition, the effect of an increment of the local equivalence ratio by the addition of volatile matter turns into a negative effect. Consequently, the negative effects overcome the positive effect in the ammonia rich condition resulting in a lower flame propagation velocity of pulverized coal/ammonia co-combustion. 相似文献
879.
Mohammed F. Hamza Eric Guibal Khalid Althumayri Thierry Vincent Xiangbiao Yin Yuezhou Wei Wenlong Li 《Molecules (Basel, Switzerland)》2022,27(20)
Sulfonic resins are highly efficient cation exchangers widely used for metal removal from aqueous solutions. Herein, a new sulfonation process is designed for the sulfonation of algal/PEI composite (A*PEI, by reaction with 2-propylene-1-sulfonic acid and hydroxylamine-O-sulfonic acid). The new sulfonated functionalized sorbent (SA*PEI) is successfully tested in batch systems for strontium recovery first in synthetic solutions before investigating with multi-component solutions and final validation with seawater samples. The chemical modification of A*PEI triples the sorption capacity for Sr(II) at pH 4 with a removal rate of up to 7% and 58% for A*PEI and SA*PEI, respectively (with SD: 0.67 g L−1). FTIR shows the strong contribution of sulfonate groups for the functionalized sorbent (in addition to amine and carboxylic groups from the support). The sorption is endothermic (increase in sorption with temperature). The sulfonation improves thermal stability and slightly enhances textural properties. This may explain the fast kinetics (which are controlled by the pseudo-first-order rate equation). The sulfonated sorbent shows a remarkable preference for Sr(II) over competitor mono-, di-, and tri-valent metal cations. Sorption properties are weakly influenced by the excess of NaCl; this can explain the outstanding sorption properties in the treatment of seawater samples. In addition, the sulfonated sorbent shows excellent stability at recycling (for at least 5 cycles), with a loss in capacity of around 2.2%. These preliminary results show the remarkable efficiency of the sorbent for Sr(II) removal from complex solutions (this could open perspectives for the treatment of contaminated seawater samples). 相似文献
880.
Rao RN Venkateswarlu N Khalid S Narsimha R Sridhar S 《Journal of chromatography. A》2006,1113(1-2):20-31
Three different sample preparation techniques (i) solid-phase extraction, (ii) reverse osmosis and (iii) vacuum distillation have been investigated and the recoveries were compared for determination of highly water-soluble benzene and stilbene sulfonic acids in aqueous environment by liquid chromatography with photodiode array (PDA) and electrospray ionization tandem mass spectrometry (LC-ESI-MS/MS). The recoveries were quite high using vacuum distillation (>90%) compared to solid phase extraction and reverse osmosis. The negative ion ESI mass spectra containing the peaks of quasimolecular ion [M-H]- allow the molecular mass determination of unknown compounds whereas the structures were proposed using fragments obtained from MS/MS analysis of [M-H]- ions. At lower fragmentation voltages only the quasimolecular ion [M-H]- was observed and as fragmentation voltages increased, it led to the formation of fragment ions corresponding to [M-H-SO3]-, [M-H-SO2]-, and SO3-. The detection limits were 1-28 microg/L with LC-ESI-MS. The sample collected from wastewater treatment plant was found to contain 21.1, 13.3, 12.1, 41.8 and 9.9 microg/L of cis-4,4(l)-diaminostilbene-2,2(l)-disulfonic acid (cis-DASDA), trans-4,4(l)-diaminostilbene-2,2(l)-disulfonic acid (trans-DASDA), 3-amino acetanilide-4-sulfonic acid (3-AASA), 4-chloroaniline-2-sulfonic acid (4-CASA), 2-chloroaniline-5-sulfonic acid (2-CASA), respectively. 相似文献