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991.
周期性结构热动力时间-空间多尺度分析 总被引:1,自引:0,他引:1
研究一种时间-空间多尺度渐近均匀化分析方法,模拟不同的极端热和动力载荷下微尺度多
相周期性结构中热动力响应问题,并建立一个广义的波动函数场控制方程描述热动力响应.
通过引入一个放大空间尺度和两个缩小时间尺度,在不同时间尺度上获得由空间非均匀性引
起的波动效应和非局部效应. 根据高阶均匀化理论在空间和时间上进行均匀化,获得高阶非
局部函数场波动方程. 并进一步用C0连续修正了高阶非局部函数场波动方程的有限元近
似解,使问题的求解避免了对有限元离散的C1连续性要求. 并与经典的空间均匀化方法
相比较,指出了经典的空间均匀化方法的局限性,进一步以一维非傅立叶热传导和热动力问
题为例,讨论了各种情况下方法的正确性与有效性. 相似文献
992.
993.
微波热致超声成像技术通过向物体发射微波脉冲, 导致物体吸收电磁波温度迅速升高, 产生瞬时压力波, 从而激发产生超声波信号, 通过传感器对产生的超声波信号进行采集并成像, 最终还原了反映物体吸收电磁波能量特性的图像, 由于此方法兼具了微波成像的高对比性和超声成像的高分辨率特点, 理论上验证了热声成像技术对早期乳腺肿瘤检测的可行性. 本实验兼顾系统成像深度和分辨率, 采用S波段的微波脉冲信号源对物体进行辐射, 利用圆形扫描方式对待测物体进行检测, 同时为了更好的验证成像性能, 本实验同时使用了肿瘤仿体及实际生物组织进行成像实验. 通过实验分析, 验证了该系统对肿瘤仿体和生物组织检测的有效性, 以及系统的高分辨率和高对比度特性, 为早期乳房肿瘤检测提供了进一步的理论支撑. 相似文献
994.
理论研究分子结构与双光子吸收性质之间的关系对于指导实验者设计与合成功能分子材料具有重要意义. 在杂化密度泛函水平上, 利用响应函数方法, 计算了一类以二乙烯硫/砜基为中心的新型电荷转移分子的双光子吸收截面, 并在相同计算水平上, 与联苯乙烯类强双光子吸收分子做了比较; 以新型电荷转移分子为基础, 利用异构效应, 设计出了可以增强双光子吸收强度的分子结构. 研究表明, 在可应用波长范围内, 该系列分子表现出较强的双光子吸收响应, 与相似共轭长度的强双光子吸收分子具有相同量级的双光子吸收截面; 二乙烯硫/砜基在分子中心作为吸电子基团可以形成有效的电荷转移分子; 改变咔唑基的连接方式可以有效提高双光子吸收截面. 该研究为实验合成新型双光子吸收分子材料提供了理论依据. 相似文献
995.
996.
997.
Cemal Özeroğlu Emine Doğan Gönül Keçeli 《Journal of Radioanalytical and Nuclear Chemistry》2011,289(2):577-586
In this study, a crosslinked copolymer bearing sodium methacrylate functional groups has been proposed to remove Cs(I) ions
from aqueous solutions. For this purpose, the crosslinked copolymer of ethylene glycol dimethacrylate (EGDM) and methacrylic
acid (MA) containing 25% MA as weight percentage was synthesized by using benzoyl peroxide (BPO)-N,N-dimethyl aniline initiator system. The available carboxyl groups in copolymer were converted to the groups of sodium methacrylate
using 2 N NaOH. The adsorption behavior of cesium ions on the densely crosslinked poly(sodium methacrylate) from aqueous solutions
were investigated by the technique of ICP-MS measurements of cesium ions in solutions. Batch adsorption method was used to
analyze the Cs(I) adsorption as a function of parameters such as the amount of adsorbent, contact time, pH of solution, initial
Cs(I) concentration and temperature. The adsorption data were evaluated by the Freundlich, Langmuir and Dubinin–Radushkevich
(D–R) isotherms. The adsorption capacity and free energy change were calculated by using D–R isotherm. The adsorption data
obtained from experimental results have been tested by the fractional power, the Elovich, the pseudo-first order and the pseudo-second
order kinetic models. 相似文献
998.
Ke D Wang X Yang Q Niu Y Chai S Chen Z An X Shen W 《Langmuir : the ACS journal of surfaces and colloids》2011,27(23):14112-14117
The interaction between dodecyltrimethylammonium bromide (DTAB) and curcumin has been studied in pH 5.0 sodium phosphate buffer using absorption and fluorescence measurements. With increasing DTAB concentration (C(DTAB)) from 0 to 20 mM, the absorption peak of curcumin at 430 nm, corresponding to the conjugated structure of curcumin, first weakens gradually into a shoulder but increases back into one peak with much higher absorption intensity. On the contrary, as C(DTAB) increases, the initial small absorption shoulder of curcumin at 355 nm, corresponding to the feruloyl unit of curcumin, first increases gradually into a clear peak but decreases back into one shoulder until almost disappeared finally. By remaining at nearly the same wavelength, the fluorescence of curcumin first decreases at C(DTAB) lower than 5 mM and then increases gradually up to C(DTAB) = 10 mM, which is followed by sharp increases of fluorescence intensity with marked blue-shifts at higher C(DTAB). The values of anisotropy and microviscosity of curcumin obtained from the fluorescence polarization technique also showed pronounced changes at different surfactant concentrations. The interaction mechanisms of DTAB with curcumin have been presented at low, intermediate, and high surfactant concentrations, which is relating to interaction forces, surfactant aggregations, as well as structural alterations of curcumin. 相似文献
999.
Hong-lin Zhang Chang-qing Kong Shu-juan Yang Hong-yan Bi Jing Li 《Journal of solution chemistry》2011,40(4):632-642
The power-time curves of the micelle formation process were determined for the nonionic surfactant Tween80/nonaqueous solvent
(DMF)/long-chain alcohol (n-heptanol, n-octanol, n-nonanol, and n-decanol) systems by titration microcalorimetry at temperatures of (298.15, 303.15, 308.15, and 313.15) K. From the power-time
curves, the CMC and
DHm\uptheta\Delta H_{\mathrm{m}}^{\uptheta} values were obtained. The corresponding values of
DGm\uptheta\Delta G_{\mathrm{m}}^{\uptheta} and
DSm\uptheta\Delta S_{\mathrm{m}}^{\uptheta} were also calculated. The relationships of the CMC with the carbon number of the alcohol, the concentration of alcohol, and
the temperature, along with the thermodynamic functions, are discussed. 相似文献
1000.
Thin wall samples of high density polyethylene (HDPE) were prepared via injection molding with different injection speeds ranging from 100 mm/s to 1200 mm/s. A significant decrease in the tensile strength and Young??s modulus was observed with increasing injection speed. In order to investigate the mechanism behind this decrease, the orientation, molecular weight, molecular weight distribution, melt flow rate, crystallinity and crystal morphology of HDPE were characterized using two-dimensional wide-angle X-ray diffraction (2D-WAXD), gel permeation chromatography (GPC), capillary rheometry and differential scanning calorimetry (DSC), respectively. It is demonstrated that the orientation, molecular weight, molecular weight distribution, melt flow rate and crystallinity have no obvious change with increasing injection speed. Nevertheless, the content of extended chain crystals or large folded chain crystals was found to decrease with increasing injection speed. Therefore, it is concluded that the decrease in tensile properties is mainly contributed by the reduced content of extended chain crystals or large folded chain crystals. This study provides industry with valuable information for the application of high speed injection molding. 相似文献