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1.
Using Stuart's energy method, the torque on the inner cylinder, for a second order fluid, in the supercritical regime is calculated. It is found that when the second normal stress difference is negative, the flow is more stable than for a Newtonian fluid and the torque is reduced. If the second normal stress difference is positive, then the flow is more stable and there is no torque reduction. Experimental data related to the present work are discussed.Nomenclature a amplitude of the fundamentals - A ij (1) , A ij (2) first and second Rivlin-Ericksen tensors - d r 2r 1 - D d/dx - E - F - g ij metric tensor - G torque on the inner cylinder in the supercritical regime - h height of the cylinders - k 0 /d 2 - k 1 /d 2 - I 1 - I 2 - I 3 - I 4 - r 1, r 2 radii of inner and outer cylinders respectively - r 0 1/2(r 1+r 2) - R Reynolds number 1 r 1 d/ 0 - R c critical Reynolds number - T Taylor number r 1 1 2 d 3 2/ 0 2 *) - T c critical Taylor number - u 1, v 1, w 1 Fundamentals of the disturbance - u i , v i , w i , (i>1) harmonics - mean velocity (not laminar velocity) - u –u 1/ar 1 1 - v v 1/Rar 1 1 - x (r–r 0)/d - , material constants - 0 viscosity - wave number d - density - 1 angular velocity of inner cylinder - tilde denotes complex conjugate  相似文献   
2.
In the present paper we describe surjective Lie and Jordan maps onto left ideals of prime noncommutative rings. Further, we describe bijective linear maps of left ideals of centrally closed prime algebras preserving commutativity.  相似文献   
3.
Amphiphilic double‐brush copolymers (DBCs) with each graft site quantitatively carrying both a hydrophilic poly(ethylene oxide) (PEO) graft and a hydrophobic polystyrene (PSt) graft are synthesized by sequential reversible addition‐fragmentation chain transfer (RAFT) polymerization and ring‐opening metathesis polymerization (ROMP). These DBCs are used as both surfactants and polyfunctional RAFT agents in the radical polymerization of St in aqueous dispersed media. Miniemulsions with narrowly dispersed St‐based nanodroplets are readily obtained after ultrasonication of the reaction mixtures. Without the presence of crosslinker, chain‐extension polymerization of St from the DBCs yields well‐defined polymeric latexes with narrow size distributions. However, with the presence of divinylbenzene (DVB) as the crosslinker, vesicular polymeric nanoparticles are formed as the major product. Such crosslinking‐induced change in morphology of the resulting latex nanomaterials may be ascribed to the increase of interfacial curvature in the heterophase systems during crosslinking polymerization. © 2014 Wiley Periodicals, Inc. J. Polym. Sci., Part A: Polym. Chem. 2014 , 52, 3250–3259  相似文献   
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It has been shown in this study that {CisPt@[n]CD} complexes formed from the anti-cancer drug cisplatin (CisPt) and cyclodextrins ([n]CD) can be a source of Pt based free radicals such as (H3N)2PtCl· and (H3N)2Pt·· species in water within a radiation environment which can produce hydrated electrons. Encapsulating CisPt within the [n]CD host takes advantage of the previously described drug delivery and reduced side effect advantages of CDs. Based on quantum mechanical modelling and literature results from other studies, it is predicted that {CisPt@[γ]CD} and the analogous 2-hydroxypropyl[β]cyclodextrin (HPBCD) complex {CisPt@HPBCD} may interact with serum albumin and engage in an enhanced permeation and retention mechanism in solid tumours, offering further synergistic advantages for radiation-{CisPt@[γ]CD} or -{CisPt@HPBCD} regimens over that of the conventional radiation-CisPt regimens in current use in anti-cancer chemoradiotherapies. Comparisons and possible advantages are made with the previously documented chemoradiosensitizing properties of the analogous cucurbit[7]uril based{CisPt@[7]CB} complex with the {CisPt@[γ]CD} and {CisPt@HPBCD} complexes suggest that all three complexes may have different and tailorable anti-tumour uses for a range of different chemotherapeutic environments or protocols.  相似文献   
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Data describing the insertion of sulphur dioxide into the carbon―tin bond of a range of substituted phenyltrimethyltin compounds in methanol and benzene solvents have been reconsidered. The reaction in methanol is cleanly second order, but the reaction in benzene has both a second‐order and third‐order component, the latter ascribable to an initial equilibrium formation of a SO2 complex with the phenyl ring followed by the insertion of a second SO2 molecule into the carbon–tin bond. Molecular orbital calculations have identified the transition states (TS) and the favoured reaction pathways for the second‐order and third‐order reaction pathways in benzene. The effects of solvents on TS and enthalpies of reaction have also been examined. New insights into the types of TS involved in electrophilic substitution reactions are revealed. Copyright © 2013 John Wiley & Sons, Ltd.  相似文献   
8.
This paper reports the synthesis and characterization of gallium nitride (GaN) thin films deposited on p-type silicon (100) substrates by using low cost spin coating method under various nitridation temperatures. This work demonstrated that spin coating with the new prepared precursor solution can be used as a versatile method for the successfully growth of GaN thin films. Furthermore, the influence of varying nitridation temperatures on the structural, morphological, and optical properties of synthesized GaN thin films were studied in this work. The GaN thin films were characterized by X-ray diffraction, field-emission scanning electron microscopy, atomic force microscopy, photoluminescence and Raman spectroscopy. All the characteristics of the GaN thin films were effectively improved with the increasing of the nitridation temperatures from 750 to 950 °C and degraded at temperature of 1,050 °C. The measured results show that nitridation temperature plays an important role in improving the crystalline quality of the GaN thin films and the most efficient nitridation temperature was at 950 °C.  相似文献   
9.
A PEG‐modified reversed migration MEEKC method was developed for simultaneous determination of six polyynes, including oplopandiol, falcarindiol, oplopandiol acetate, (11S, 16S, 9Z)‐9,17‐octadecadiene‐12,14‐diyne‐1,11,16‐triol,1‐acetate, oplopantriol B, and oplopantriol A, in Oplopanax horridus and Oplopanax elatus. The running buffer containing 0.8% v/v ethyl acetate, 3.8% w/v SDS, 6.6% v/v n‐butanol in 20 mM phosphate buffer (pH 2.5), followed by mixing with propan‐2‐ol at 30% v/v and PEG‐1000 at 15% w/v, was applied in the analysis. The proposed method was successfully applied to determine the six polyynes in five samples of Oplopanax horridus and one of O. elatus. The result showed that the types and amounts of polyynes present were obviously different when comparing the two herbs. Besides, the developed PEG‐modified reversed MEEKC method might be suitable for the analysis of hydrophobic analytes in herbal medicines.  相似文献   
10.
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