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131.
The primary objective of the present article is to understand how the geometric constraints at the surfactant head affect the lipase activity in the reverse micellar interface. To resolve this issue, surfactants were designed and synthesized, and activity was measured in /water/isooctane/n-hexanol reverse micellar systems at z ([alcohol]/[surfactant])=5.6, pH 6.0 (20 mM phosphate), 25 degrees C across a varying range of W0 ([water]/[surfactant]) using p-nitrophenylalkanoates as the substrate. It was observed that lipase activity increases from surfactants to with the increment in surface area per molecule (Amin) because of the substitution by the bulky tert-butyl group at the polar head. However, the activity was found to be similar for despite an enhancement in the hydrophilic moieties at the interface. This unchanged lipase activity is presumably due to the comparable surface area of to originating from the rigidity at the surfactant head. Noticeably, the enzyme activity improved from with the simultaneous increment of both the hydroxyl group and the flexibility of the headgroup whereas that for increased exclusively with the flexibility of the headgroup. The common parameter in both groups of surfactants and is the flexibility of the headgroup, which possibly enhance Amin and consequently the lipase activity. Thus, the geometric constraints at the surfactant headgroup play a crucial role in modulating the lipase activity profile probably because of the variation in interfacial area.  相似文献   
132.
We present a versatile, optical fiber coupled light emitting diode (LED) light source based flow-through optical absorbance detector. The LED source is readily changeable. Optical fibers are used to carry light from the electronics/display unit to a reflective flow-through cell and back. The cell can thus be located remotely from the electronics unit and the umbilical connection is not susceptible to electrical noise. The noise level of this detector with LEDs of different emission maxima were observed to be in the range of 3-20 muAU under actual use conditions, with a maximum short term drift of 4 muAU/min after the initial warm-up period. When the analyte absorbance is well matched with the source emission characteristics, the detector response is linear with concentration over at least two orders of magnitude. The liquid flow path through the cell is linear with a large exit aperture such that bubbles are not trapped in the optical path. The optical arrangement is such that the incident light crosses the liquid flow orthogonally and is reflected back by a rear mirror to the receiver fiber. This arrangement reduces the refractive index sensitivity by an order of magnitude relative to conventional Z-path flow cells.  相似文献   
133.
Ionic liquid 1-ethyl-3-methylimidazolium acetate ([EMIM]oAc) was employed for the pretreatment of sugarcane bagasse (SCB) and extraction of lignin, a potentially valuable by-product of the biofuel industry. Response surface methodology based on central composite design was exploited and thereby an empirical model, exhibiting a coefficient of determination, R2, of 0.9890, was established to optimize lignin recovery. In particular, a maximum lignin yield, equal to 90.1%, was calculated at the optimal pretreatment conditions, namely time: 120 min, temperature: 140 °C, and ionic liquid to bagasse ratio equal to 20:1 (wt/wt). The presence of guaiacyl and syringyl rings in lignin was confirmed by Fourier transform infrared spectroscopy (FTIR); whereas UV–Vis spectrophotometry showed that both p-coumaric acid and ferulic acid were contained in the lignin. Thermal analysis indicated a maximum decomposition rate of 2%/°C at 265 °C while Gel permeation chromatography analysis revealed that the molecular weight (Mw) of recovered lignin was equal to 1769 g/mol. Comparison of FTIR spectra of pretreated and untreated bagasse showed a negligible presence of lignin in the pretreated samples. Maximum delignification of bagasse after pretreatment was thus ensured. Thermal stability of the ionic liquid towards recyclability was proven by thermogravimetric analysis. The present study established adequate performance of neat and recycled ([EMIM]oAc) with regard to lignin recovery from SCB.  相似文献   
134.
We describe a light emitting diode (LED) based multi-reflection capillary scale absorbance detector based on both square and round capillaries and compare their performance with a conventional single-pass on-tube detector. The optical path length is extended by silver coating, the external surface of the capillary. The reflective geometry has been reported to be less prone to artifacts induced by refractive index changes; we do find this to be true. Although the detection volume/illuminated volume is increased some, a multi-reflection cell based on a 180 μm bore capillary with a ∼2-cm long illuminated volume shows over a 50-fold gain in signal-to-noise (S/N) compared to a single-pass on-tube configuration with the same capillary. The limit of detection (LOD) is 4.4 fmol (2.6 pg, 1 μL of 22.0 nM injected dye) BTB under pulseless (pneumatic) flow conditions. The cells behave as multipath devices where the effective path lengths are greater at low absorbance values. In our experiments, where non-coherent light is launched through optical fibers that are large compared to capillary bore dimensions, increase in the effective path length of the cell do not occur in a predictable fashion with the angle of incidence of the light beam. Although the effective path length almost linearly increases with increasing distance between the light entry and exit windows, the absolute values of the effective path lengths are always lower than this physical distance, suggesting that after some passage through the solution, light largely travels through or along the glass wall. Square capillaries have better light transmission and offer some performance advantages. Multi-reflection cells can indeed be of value for sensitive detection in microflow systems.  相似文献   
135.
The authors have used atomistic molecular dynamics (MD) simulations to study the structure and dynamics of water molecules inside an open ended carbon nanotube placed in a bath of water molecules. The size of the nanotube allows only a single file of water molecules inside the nanotube. The water molecules inside the nanotube show solidlike ordering at room temperature, which they quantify by calculating the pair correlation function. It is shown that even for the longest observation times, the mode of diffusion of the water molecules inside the nanotube is Fickian and not subdiffusive. They also propose a one-dimensional random walk model for the diffusion of the water molecules inside the nanotube. They find good agreement between the mean-square displacements calculated from the random walk model and from MD simulations, thereby confirming that the water molecules undergo normal mode diffusion inside the nanotube. They attribute this behavior to strong positional correlations that cause all the water molecules inside the nanotube to move collectively as a single object. The average residence time of the water molecules inside the nanotube is shown to scale quadratically with the nanotube length.  相似文献   
136.
The determination of perchlorate in complex matrices by ion chromatography (IC) with an online preconcentration and preelution technique is discussed. The method was applied to different sample types containing large concentrations of matrix anions that would otherwise interfere with analysis via conventional IC. The present approach was highly effective in removing most of the matrix anions and was thus resistant to the interferences commonly encountered in a high ionic strength background. Method performance was evaluated by analyzing for low-level perchlorate in synthetic high ionic strength solutions, tissue extracts, and hydroponic nitrate fertilizer samples. Not only is it easier to practice the present method compared to USEPA Method 314.0, but for most of these samples the present approach provided equal to or better recovery of perchlorate than Method 314.0. With a sample of specific conductance 12,650 μS cm−1, for example, the present method provided a perchlorate recovery of 101% at the 25 μg L−1 level versus 89% by EPA Method 314.0. Method detection limits of perchlorate in hydroponic fertilizer samples with this method (130-190 μg kg−1) are the lowest thus far reported.  相似文献   
137.
Singlet fission is a process by which two molecular triplet excitons are generated subsequent to the absorption of one photon. Molecules that enable singlet fission have triplet state energy at least half of the bright singlet state energy. This stringent energy criteria have challenged chemists to device new molecular and supramolecular design principles to modulate the singlet–triplet energy gap and build singlet fission systems from a wide range of organic chromophores. Herein, we report for the first time intramolecular singlet fission in the seminal naphthalenediimide (NDI) scaffold constrained in a push–pull cyclophane architecture, while individually the NDI chromophore does not satisfy the energy criterion. The challenging synthesis of this highly contorted push–pull cyclophane is possible from the preorganized pincer-like precursor. The special architecture establishes the shortest co-facial NDI⋯NDI contacts (3.084 Å) realized to date. Using broadband femtosecond transient absorption, we find that the correlated T–T pair forms rapidly within 380 fs of photoexcitation. Electronic structure calculations at the level of state-averaged CASSCF (ne,mo)/XMCQDPT2 support the existence of the multi-excitonic T–T pair state, thereby confirming the first example of singlet exciton fission in a NDI scaffold.

We report for the first-time intramolecular singlet fission (SF) in the naphthalenediimide (NDI) scaffold constrained in a cyclophane architecture, while individually the NDI units does not satisfy the requisite energy criterion for SF.  相似文献   
138.
139.
Headspace solid-phase micro-extraction (HS-SPME) and ultrasonic solvent extraction (USE) were used for red clover honey volatiles extraction. The extracts were analysed using gas chromatography and mass spectrometry (GC-MS). Lilac aldehyde isomers dominated in the headspace (individual range from 7.6 % to 21.4 %) followed by phenylacetaldehyde (10.1–31.2 %) and benzaldehyde (7.0–15.7 %). Higher aliphatic alcohols and hydrocarbons were the predominant constituents of the honey extracts. The honey and its extracts exhibited rather weak anti-radical activity (DPPH assay) and total antioxidant activity (FRAP assay). On the other hand, the honey’s inhibitive properties towards the corrosion of AA 2017A alloy in NaCl solution (potentiodynamic polarisation and potentiostatic pulse measurements) revealed the honey to be a very good anodic inhibitor (efficiency up to 76 %) while the honey extracts (USE) showed better inhibition efficacy.  相似文献   
140.
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