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141.
Spin-lattice relaxation mechanisms in kaolinite have been reinvestigated by magic-angle spinning (MAS) of the sample. MAS is useful to distinguish between relaxation mechanisms: the direct relaxation rate caused by the dipole-dipole interaction with electron spins is not affected by spinning while the spin diffusion-assisted relaxation rate is. Spin diffusion plays a dominant role in 1H relaxation. MAS causes only a slight change in the relaxation behavior, because the dipolar coupling between 1H spins is strong. 29Si relaxes directly through the dipole-dipole interaction with electron spins under spinning conditions higher than 2 kHz. A spin diffusion effect has been clearly observed in the 29Si relaxation of relatively pure samples under static and slow-spinning conditions. 27Al relaxes through three mechanisms: phonon-coupled quadrupole interaction, spin diffusion and dipole-dipole interaction with electron spins. The first mechanism is dominant, while the last is negligibly small. Spin diffusion between 27Al spins is suppressed completely at a spinning rate of 2.5 kHz. We have analyzed the relaxation behavior theoretically and discussed quantitatively. Concentrations of paramagnetic impurities, electron spin-lattice relaxation times and spin diffusion rates have been estimated. 相似文献
142.
We study the large-time behavior and rate of convergence to the invariant measures of the processes dX
(t)=b(X)
(t)) dt + (X
(t)) dB(t). A crucial constant appears naturally in our study. Heuristically, when the time is of the order exp( – )/2 , the transition density has a good lower bound and when the process has run for about exp( – )/2, it is very close to the invariant measure. LetL
=(2/2) – U · be a second-order differential operator on d. Under suitable conditions,L
z has the discrete spectrum
- \lambda _2^\varepsilon ...and lim \varepsilon ^2 log \lambda _2^\varepsilon = - \Lambda \hfill \\ \varepsilon \to 0 \hfill \\ \end{gathered} $$
" align="middle" vspace="20%" border="0"> 相似文献
143.
D. Ugolini M. -H. Tuilier J. Eitle S. Schelz J. Q. Wang P. Oelhafen 《Applied Physics A: Materials Science & Processing》1990,51(6):526-536
Polymeric styrene films with thicknesses ranging from about one nm up to a few m have been deposited by means of a direct ion beam deposition (IBD) technique. The deposition energy, which can be chosen independently of the parameters which govern the plasma conditions, has been varied between few eV and 1000 eV. The correlation between the deposition parameters and the resulting film properties in terms of the electronic structure is discussed. The in situ characterization by electron spectroscopy has proved to be a very useful characterization method and ultraviolet photoelectron spectroscopy in particular revealed an extremely high sensitivity to structural differences in the deposited films. The polymeric films have also been characterized by scanning electron microscopy and optical spectroscopy. These techniques have also served to compare films prepared by the direct IBD technique with films obtained by standard rf plasma polymerization (RFPP) in a tubular reactor. Significant differences have been found which are dependent on the deposition parameters; these are discussed in detail.Department of Chemical Engineering, Beijing Institute of Technology, P.O. Box 327 Beijing, 100081 Beijing, P.R. China 相似文献
144.
Summary As shown in preceding papers of the authors, the verification of anR-convergence order for sequences coupled by a system (1.1) of basic inequalities can be reduced to the positive solvability of system (3.3) of linear inequalities. Further, the bestR-order
implied by (1.1) is equal to the minimal spectral radius of certain matrices composed from the exponents occuring in (1.1). Now, these results are proven in a unified and essentially simpler way. Moreover, they are somewhat extended in order to facilitate applications to concrete methods. 相似文献
145.
J. Hastad 《Combinatorica》1988,8(1):75-81
We prove that given a point
outside a given latticeL then there is a dual vector which gives a fairly good estimate for how far from the lattice the vector is. To be more precise, there is a set of translated hyperplanesH
i, such thatL
iHi andd(
iHi)(6n
2+1)–1
d(
,L).Supported by an IBM fellowship. 相似文献
146.
G. Carelli N. Ioli A. Moretti D. Pereira F. Strumia R. Densing 《Applied physics. B, Lasers and optics》1988,45(2):97-100
FIR laser lines close to the N+
3
P
2–3
P
1 transition at 122 m can be used as a local oscillator for heterodyne detectors. The frequencies of some candidate laser lines from CH2F2,13CH3OH, CD3OD, and CD3OH have been measured and the output power of the most interesting lines has been optimized. 相似文献
147.
蚕蛹甲壳素的脱色方法与机理探讨 总被引:10,自引:0,他引:10
研究了从粗甲壳素 (分离蚕蛹蛋白质后的残渣 )中提取蚕蛹甲壳素的工艺条件 ,探索了H2 O2 氧化脱色方法。实验结果表明 ,在 70℃的水浴中 ,按照m(蚕蛹渣 )∶m(5 %氢氧化钠 ) =30∶80的质量比处理 2h ,可脱净残余蛋白 ,得到黑褐色的粗蚕蛹甲壳素。用H2 O2 脱色漂白 ,工艺条件为 :6 5~ 70℃ ,pH值为 8 5± 0 5 ,时间 5h ,m (蚕蛹渣 )∶m(30 %H2 O2 ) =5 0∶130。所得甲壳素白度为 30 % ,收率为 2 5 %。双氧水脱除蚕蛹甲壳素颜色的机理可能是H2 O2 分解的O2 -2 作用于铁硫蛋白与细胞色素复合物体系中的硫 ,将体系中半胱氨酸硫氧化成亚砜 ,使得色蛋白与甲壳素相连的键断开 ,从而使色素从甲壳素上分离下来。 相似文献
148.
W. Fleischhacker K. Florkova B. Richter 《Monatshefte für Chemie / Chemical Monthly》1994,125(3):345-353
Summary Following our concept of rather new structural variations in the nitrogen region of morphine alkaloids we describe the first synthesis of N/C-10-bridged tertiary bases. 相似文献
149.
镀铜铁屑-H_2O_2催化氧化降解含酚废水 总被引:2,自引:0,他引:2
采用镀铜铁屑代替传统Fenton体系中的FeSO4作为催化剂,通过改变H2O2与镀铜铁屑的投加量、溶液的pH值、反应温度、反应时间等条件,研究了该体系对处理苯酚废水的影响。结果表明,常温下处理实际含酚印染废水,在pH值为4~6,30%H2O2 12mL/L,镀铜铁屑5g/L,反应时间为45min时,COD去除率可达96%,其CODCr从5827mg/L降至419mg/L,色度从2000降至30,符合国家三级排放标准。 相似文献
150.
Gáti T Simon A Tóth G Magiera D Moeller S Duddeck H 《Magnetic resonance in chemistry : MRC》2004,42(7):600-604
Adducts of four phosphine chalcogenides with the chiral dirhodium complex ([Rh-Rh]) were investigated by variable-temperature 1H and 31P NMR spectroscopy in order to compare their properties as axial ligands. Whereas the selenide (1) and the sulfide (2) are strong ligands with electrostatic attraction and, in addition, a significant orbital (HOMO-LUMO) interaction, the phosphine oxide compounds (P=O) bind primarily via electrostatic attraction and are relatively weak donors. Moreover, the overall bond strength in these adducts depends on steric congestion around the P=O group. 相似文献
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