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91.
利用原子转移自由基聚合(Atom Transfer Radical Polymerization, ATRP)合成了分子量分布较窄的聚甲基丙烯酸N, N-二甲氨基乙酯{Poly\[2 (diethylamino)ethylmethacry-late], PDMAEMA}并通过对液体核磁共振氢谱(1H NMR)化学位移以及弛豫时间(T1、T2)的测量,研究了聚合物PDMAEMA的温度敏感、pH敏感以及离子敏感3种环境敏感行为. 发现聚合物链段的运动性,以及温度和离子强度诱导的相变行为,都与体系的pH值具有强依赖关系. 室温下,聚合物链段的运动性随pH值的增大而降低. 酸性条件下,聚合物表现出离子敏感性,而不表现出温度敏感性. 碱性条件下,聚合物表现出温度敏感性,不表现出离子敏感性. 相似文献
92.
为了实时探测离子土固化剂(ISS)在固土过程中的阳离子交换量(CEC),采用激光击穿光谱技术(LIBS),对ISS处理后的土壤溶液中的K、Ca、Na、Mg、Al、Si这6种离子含量进行探测。分别对由不同配比(1∶100、1∶200和1∶300)的ISS处理过的高岭土、膨胀土、红粘土等5种标准土壤进行了研究,结果表明:同一土壤中的各种离子随ISS配比的变化趋势各不相同;不同土壤与ISS作用的效果各不相同;ISS的配比并非越高越好。这些工作为ISS固化机理的研究提供实验依据,而利用激光击穿光谱技术进行探测的方式为ISS固化机理的研究提供了新的思路。 相似文献
93.
Margarida S. Miranda José E. Rodríguez‐Borges Joaquim C. G. Esteves da Silva Xerardo García‐Mera 《Journal of Physical Organic Chemistry》2012,25(6):515-522
The cycloaddition between glyoxylate imines possessing two chiral auxiliaries, N‐(R)‐ or N‐(S)‐1‐phenylethyl and 8‐phenylmenthyl or 8‐phenylneomenthyl, and cyclopentadiene is described. Computational calculations using density functional theory with the Becke, three‐parameter, Lee–Yang–Parr functional and the 6‐31G(d) basis set were performed to better understand the highly diastereoselective mechanism and the exo‐selectivity observed experimentally for these ionic aza‐Diels–Alder reactions. Copyright © 2011 John Wiley & Sons, Ltd. 相似文献
94.
Comments on a recent article on an enhanced polarization mechanism for the metal cations modified amorphous TiO2 based electrorheological materials are presented, based upon an examination of the yield stress, which is a function of electric-field
strength, of the materials. Using the deduced critical electric-field strengths, we find that the universal yield stress equation
proposed collapses the data given by Qing Wu, Bin Yuan Zhao, Chen Fang, Ke Ao Hu, Eur. Phys. J. E 17, 63 (2005), onto a single curve. 相似文献
95.
Subba Reddy ChV Jin AP Zhu QY Mai LQ Chen W 《The European physical journal. E, Soft matter》2006,19(4):471-476
A sodium ion-conducting polymer electrolyte based on polyvinyl pyrrolidone (PVP) complexed with NaClO4 was prepared using the solution-cast technique. The cathode film of V2O5 xerogel modified with polyvinyl pyrrolidone was prepared using the sol-gel method. Investigations were conducted using X-ray
diffractometry (XRD), Fourier transformation infrared (FT-IR) spectroscopy. The ionic conductivity and transference number
measurements were performed to characterize the polymer electrolyte for battery applications. The transference number data
indicated that the conducting species in these electrolytes are the anions. Using the electrolyte, electrochemical cells with
a configuration Na/(PVP + NaClO4)/V2O5 modified by (PVP) were fabricated and their discharge profiles studied. 相似文献
96.
Transport properties of glass-formers near glass transition reflect the varying degrees of the sensitivity of the solid-like dynamics and structures with respect to temperature, depending on their fragility. Notably, however, most glasses resume Arrehenius transport behavior upon onset of vitrification. To address this phenomenon a theory of the self-diffusion coefficient and viscosity is developed on the basis of a model constructed for the generalized excluded volume of glass-formers described by the generic van der Waals equation of state. The molecular clustering behavior of a glass-former is exploited in terms of an order parameter that measures the concentration of glassy, clustered molecules, which is then related to the excluded volume. The formulas arrived therefrom are shown to excellently account for the self-diffusion coefficient and viscosity of various glass-formers over the entire fragility spectrum studied experimentally: e.g., GeO2, silica, ethanol, glycerol, diopside, propylene carbonate, o-terphenyl, tris-napthylbenzene, toluene, and so on. The excluded volume effect thus investigated is shown to essentially characterize the fragility of the glass-formers. The resulting theory not only predicts for fragile glass-formers to resume Arrehenius transport behavior upon the onset of the glass transition, but also explains a crossover between strong and fragile glass-formers in their diffusivity and viscosity profiles as vitrification sets in. 相似文献
97.
We present the results of Monte Carlo simulations of the liquid-vapor interface of sodium-cesium alloys. The longitudinal density profile of each alloy shows that the liquid-vapor interface consists of a well-defined monolayer of cesium sitting on top of a slab of the bulk alloy. Underneath the monolayer there is a slight excess of sodium. A comparison with a van der Waals analog of one of the alloys shows that the presence of the well-defined monolayer of cesium on the outside of the liquid-vapor interface is a feature peculiar to metallic mixtures. The transverse pair correlation functions of the cesium monolayer are insensitive to the composition of the bulk of the slab. 相似文献
98.
S. Pleutin A. Ovchinnikov 《The European Physical Journal B - Condensed Matter and Complex Systems》2001,23(4):521-531
The static polarizability of cylindrical systems is shown to have a strong dependence on a uniform magnetic field applied
parallel to the tube axis. This dependence is demonstrated by performing exact numerical diagonalizations of simple cylinders
(rolled square lattices), armchair and zig-zag carbon nanotubes (rolled honeycomb lattices) for different electron-fillings.
At low temperature, the polarizability as function of the magnetic field has a discontinuous character where plateau-like
region are separated by sudden jumps or peaks. A one to one correspondence is pointed out between each discontinuity of the
polarizability and the magnetic-field induced cross-over between the ground state and the first excited state. Our results
suggest the possibility to use measurements of the static polarizability under magnetic field to get important informations
about excited states of cylindrical systems such as carbon nanotubes.
Received 29 March 2001 and Received in final form 8 August 2001 相似文献
99.
R.N. Bulakhe N.M. Shinde R.D. Thorat S.S. Nikam C.D. Lokhande 《Current Applied Physics》2013,13(8):1661-1667
In this paper, we report structural, morphological, electrical studies of copper iodide (CuI) thin films deposited onto glass substrates by chemical bath deposition (CBD) and successive ionic layer adsorption and reaction (SILAR) methods. CuI thin films were characterized for their structural, morphological and wettability studies by means of X-ray diffraction (XRD), FT-Raman spectroscopy, scanning electron microscopy (SEM), optical absorption, and contact angle measurement methods. Thickness of thin films was 1 ± 0.1 μm measured by gravimetric weight difference method. The CuI thin films were nanocrystalline, with average crystal size of ~60 nm. The FT-IR study confirmed the formation of CuI on the substrate surface. SEM images revealed the compact and cube like structure for CuI thin films deposited by CBD and SILAR methods, respectively. Optical absorption study revealed optical energy gaps as 2.3 and 3.0 eV for CBD and SILAR methods, respectively. Wettability study indicated that CuI thin films deposited by SILAR method are more hydrophobic as compared to CBD method. 相似文献
100.
TCs-Fe(Ⅲ)体系离子液体气浮浮选荧光光谱法分离/富集四环素类抗生素残留的研究 总被引:1,自引:0,他引:1
将离子液体应用于气浮溶剂浮选,建立了一种分离/富集四环素类(tetracyclines, TCs)抗生素的新方法——离子液体气浮溶剂浮选。最优化浮选条件为:以1-己基-3-甲基咪唑六氟磷酸盐([Hmim]PF6)和乙酸乙酯(EA)的混合溶剂(φ=1/0.9)为浮选剂,以Fe(Ⅲ)为捕集剂,pH值为7.6,气体流速为40 mL·min-1,浮选时间为50 min。富集TCs-Fe(Ⅲ)配合物的[Hmim]PF6-EA相用荧光光谱法直接测定,其线性回归方程为F=246.5c+4.32(c: μg·10 mL-1),相关系数r=0.999 1。实测了鱼塘表面水体和沉积物中四环素类抗生素的含量,加标回收率达到94.2%~100.4%,RSD<3.2%(n=5)。红外光谱分析显示TCs-Fe(Ⅲ)配合物没有和离子液体发生反应,离子液体在气浮溶剂浮选中只起到溶剂作用。该方法适合于环境水样中痕量四环素类抗生素的分离/富集及分析。 相似文献