全文获取类型
收费全文 | 2043篇 |
免费 | 415篇 |
国内免费 | 219篇 |
专业分类
化学 | 1400篇 |
晶体学 | 6篇 |
力学 | 113篇 |
综合类 | 21篇 |
数学 | 279篇 |
物理学 | 858篇 |
出版年
2024年 | 2篇 |
2023年 | 49篇 |
2022年 | 50篇 |
2021年 | 83篇 |
2020年 | 86篇 |
2019年 | 87篇 |
2018年 | 72篇 |
2017年 | 64篇 |
2016年 | 80篇 |
2015年 | 90篇 |
2014年 | 115篇 |
2013年 | 127篇 |
2012年 | 190篇 |
2011年 | 213篇 |
2010年 | 157篇 |
2009年 | 115篇 |
2008年 | 143篇 |
2007年 | 120篇 |
2006年 | 129篇 |
2005年 | 110篇 |
2004年 | 73篇 |
2003年 | 63篇 |
2002年 | 78篇 |
2001年 | 51篇 |
2000年 | 43篇 |
1999年 | 38篇 |
1998年 | 37篇 |
1997年 | 28篇 |
1996年 | 23篇 |
1995年 | 16篇 |
1994年 | 14篇 |
1993年 | 10篇 |
1992年 | 22篇 |
1991年 | 13篇 |
1990年 | 14篇 |
1989年 | 7篇 |
1988年 | 7篇 |
1987年 | 12篇 |
1986年 | 6篇 |
1985年 | 4篇 |
1984年 | 3篇 |
1983年 | 3篇 |
1982年 | 4篇 |
1981年 | 4篇 |
1980年 | 5篇 |
1977年 | 2篇 |
1976年 | 2篇 |
1969年 | 2篇 |
1957年 | 2篇 |
1906年 | 1篇 |
排序方式: 共有2677条查询结果,搜索用时 78 毫秒
71.
纳米氧化铝微柱富集-等离子体发射光谱法测定植物中痕量稀土元素 总被引:1,自引:0,他引:1
以负载了1-苯基-3-甲基-4-苯甲酰基-吡唑酮[5](PMBP)的纳米氧化铝为微柱吸附材料,采用等离子体原子发射光谱法(ICP-AES),系统地研究了其在动态条件下对稀土离子Sc^3 、Y^3 和La^3 的吸附性能,并确定了最佳吸附及解脱条件。实验结果表明:在pH为4.5时,分析物均可被上述吸附材料定量吸附;用0.5moL/L盐酸溶液可将吸附在微柱上的稀土离子完全解脱。本法对Sc^3 、Y^3 和La^3 的检出限分别为0.16、0.19和0.39μg/L;相对标准偏差(RSD)分别为2.7%、3.2%和1.6%(n=9,C=0.5mg/L)。方法应用于植物标样中痕量Sc、Y和La的测定,其测定值与标样值吻合很好。 相似文献
72.
106Ru chloro and nitrosyl-nitrato complexes in sea water were separated into several species by continuous electrophoresis on
a filter paper curtain. Biological uptake experiments were carried out on sea algae Fucus virsoides with fractionated106Ru chloro and nitrosyl-nitrato complex species in sea water. The biological uptake of106Ru chloro complex species was about 8 times higher than the uptake of106Ru nitrosyl-nitrato species. Electrophoretically most mobile electrically positively charged cationic species in both systems
also showed about 8 times higher biological uptake than the most mobile negatively charged anionic species. A close relation
of the biological uptake to the sign of the electrical charge and the electrophoretic mobility of the species is demonstrated.
The results are discussed with respect to possible danger to the biological environment as a consequence of the aging of ruthenium
species in sea water resulting from106Ru waste disposal to the sea from a nuclear reprocessing plant.
On leave of absence from the National Institute of Radiological Sciences, 9-1, 4-chome, Anagawa, Chiba-shi, Japan, on a fellowship
from The Science and Technology Agency of the Japanese Govemment. 相似文献
73.
Nanosized aluminum nitride hollow spheres were synthesized by simply heating aluminum nanoparticles in ammonia at 1000 °C. The as-synthesized sphere shells are polycrystalline with cavity diameters ranging from 15 to 100 nm and shell thickness from 5 to 15 nm. The formation mechanism can be explained by the nanoscale Kirkendall effect, which results from the difference in diffusion rates between aluminum and nitrogen. The Al nanoparticles served as both reactant and templates for the hollow sphere formation. The effects of precursor particle size and temperature were also investigated in terms of product morphology. Room temperature cathode luminescence spectrum of the nanosized hollow spheres showed a broad emission band centered at 415 nm, which is originated from oxygen related luminescence centers. The hollow structure survived a 4-h heat treatment at 1200 °C, exhibiting excellent thermal stability. 相似文献
74.
Amidinothiourea immobilized glass bead (AGB) was applied as the microcolumn packing for the flow-injection online separation
and preconcentration of Au(III) and Pd(II) coupled with FAAS determination. The peak-area absorbance (A) and the peak-height
absorbance (H) were all used as the evaluating modes. Au(III) and Pd(II) in 0.50 M HCl solution were absorbed onto AGB completely
and then eluted into AAS with thiourea solution. Base metal ions with a concentration of 2.0 mg/mL and anions with a concentration
of 20.0 mg/mL caused no interference in the determination of Au(III) and Pd(II). The LODs of Au(III) and Pd(II) for a preconcentration
time of 60 s with a sampling flow rate of 5.0 mL/min for 0.20 μg/mL of Au(III) and 0.30 μg/mL of Pd(II) were 2.7 and 6.5 ng/mL
with the H mode and 4.6 and 10.2 ng/mL with the A mode, respectively. The RSD of seven replicate determinations of 0.20 μg/mL
of Au(III) and 0.30 μg/mL of Pd(II) were 0.018 and 0.024 for the H mode and 0.013 and 0.018 for the A mode, respectively.
The method was successfully applied to the determination of Au and Pd in real samples.
__________
From Zhurnal Analiticheskoi Khimii, Vol. 60, No. 10, 2005, pp. 1023–1029.
Original English Text Copyright ? 2005 by Liu, Pu, Su.
The text was submitted by the authors in English. 相似文献
75.
76.
A method is presented that allows novel measurement of the effect of microstructure on the oxygen permeability of highly condensed, polycrystalline phospholipid monolayers. Oxygen permeability of the polycrystalline shell coating a stationary microbubble is measured directly using an apposing microelectrode in the induced transfer mode and modeling oxygen flux through the shell and intervening aqueous medium. Varying cooling rate through the phospholipid main phase transition permits control of shell microstructure by manipulation of crystalline domain size and shape. Domain boundary density, defined as the ratio of the mean domain perimeter to the mean domain area, of the microbubble shell is determined by fluorescence microscopy. Oxygen permeability was shown to increase linearly with domain boundary density at a constant phospholipid acyl chain length and, accordingly, was shown to decrease exponentially with increasing chain length at a constant domain boundary density. Modification of the energy barrier theory to account for microstructural effects, in terms of the domain boundary density, provides a general equation to model passive transport through polycrystalline monolayer films. Results from this method show promise in determining the gas transport kinetics of medical microbubbles and the gas exchange characteristics of biological monolayers. 相似文献
77.
Yun Gong Changwen Hu Hui Li Wanlong Pan Xueli Niu Zhifa Pu 《Journal of Molecular Structure》2005,740(1-3):153-158
Two nickel (imidazole) complexes, Ni(im)6Cl2·4H2O (1) and Ni(im)6(NO3)2 (2) (im=imidazole) have been synthesized and characterized by elemental analysis, IR, UV, TG and single crystal X-ray diffraction. 1 crystallizes in the triclinic space group P-1 with a=8.800(6) Å, b=9.081(6) Å, c=10.565(7) Å, =75.058(9)°, β=83.143(8)°, γ=61.722(8)°, V=718.3(8) Å3, Z=1 and R1 (wR2)=0.0469 (0.1497). 2 crystallizes in the trigonal space group R-3 with a=12.370(6) Å, b=12.370(6) Å, c=14.782(14) Å, =90.00°, β=90.00°, γ=120.00°, V=1959(2) Å3, Z=3 and R1 (wR2)=0.0358 (0.0955). 1 and 2 exhibit different supramolecular network due to their different counter anions and different hydrogen bonding connection. In compound 1, [Ni(im)6]2+ cation and counter anions Cl− alternatively array in an ABAB fashion via N–HCl hydrogen bonding. In compound 2, the plane of each NO32− is almost parallel and each NO32− connect three different [Ni(im)6]2+ cations via N–HO hydrogen bonding. 相似文献
78.
In pH 6.0-11.2 Britton-Robinson buffer solution, binding of heparin with crystal violet (CV) can result in a significant enhancement of resonance Rayleigh scattering (RRS) and resonance non-linear scattering, such as frequency doubling scattering (FDS) and second-order scattering (SOS). Their maximum scattering wavelengths, λex/λem, appear at 492 nm/492 nm for RRS, 984 nm/492 nm for FDS and 492 nm/984 nm for SOS, respectively. The optimum conditions of the reaction, the influencing factors and the relationship between the three scattering intensities and the concentration of heparin have been investigated. New methods for the determination of trace amounts of heparin based on the RRS, FDS and SOS methods have been developed. The methods exhibit high sensitivities, the detection limit for heparin is 2.9 ng ml−1 for the RRS method, 3.5 ng ml−1 for the FDS method and 3.3 ng ml−1 for the SOS method. The methods have good selectivity and were applied to the determination of heparin in heparin sodium injection samples with satisfactory results. 相似文献
79.
Chou HC Hsu CH Cheng YM Cheng CC Liu HW Pu SC Chou PT 《Journal of the American Chemical Society》2004,126(6):1650-1651
A molecular recognition concept exploiting multiple-hydrogen-bond fine-tuned excited-state proton-transfer (ESPT) was conveyed using 3,4,5,6-tetrahydrobis(pyrido[3,2-g]indolo)[2,3-a:3',2'-j]acridine (1a). The catalytic type 1a/carboxylic acids hydrogen-bonding (HB) complexes undergo ultrafast ESPT, resulting in an anomalously large Stokes shifted tautomer emission (lambdamax approximately 600 nm). Albeit forming a quadruple HB complex, ESPT is prohibited in the noncatalytic-type 1a/urea complexes (lambdamax approximately 430 nm). The HB configuration tuning ESPT properties lead to a feasible design for sensing multiple-HB-site analytes of biological interest. 相似文献
80.
Research on Chemical Intermediates - We report a novel method for fabrication of a nano-TiO2/polyimide (PI)/Ni foam photoanode. Characterization results indicated that porous nanostructured TiO2... 相似文献