全文获取类型
收费全文 | 907篇 |
免费 | 28篇 |
国内免费 | 19篇 |
专业分类
化学 | 598篇 |
晶体学 | 3篇 |
力学 | 38篇 |
数学 | 108篇 |
物理学 | 207篇 |
出版年
2023年 | 8篇 |
2022年 | 15篇 |
2021年 | 13篇 |
2020年 | 14篇 |
2019年 | 11篇 |
2018年 | 11篇 |
2017年 | 8篇 |
2016年 | 20篇 |
2015年 | 21篇 |
2014年 | 27篇 |
2013年 | 39篇 |
2012年 | 63篇 |
2011年 | 94篇 |
2010年 | 45篇 |
2009年 | 40篇 |
2008年 | 58篇 |
2007年 | 43篇 |
2006年 | 51篇 |
2005年 | 48篇 |
2004年 | 45篇 |
2003年 | 32篇 |
2002年 | 26篇 |
2001年 | 21篇 |
2000年 | 37篇 |
1999年 | 19篇 |
1998年 | 9篇 |
1997年 | 6篇 |
1996年 | 8篇 |
1995年 | 7篇 |
1994年 | 4篇 |
1993年 | 12篇 |
1992年 | 9篇 |
1991年 | 8篇 |
1990年 | 7篇 |
1989年 | 3篇 |
1988年 | 7篇 |
1987年 | 3篇 |
1986年 | 4篇 |
1985年 | 6篇 |
1984年 | 7篇 |
1983年 | 2篇 |
1982年 | 4篇 |
1981年 | 4篇 |
1980年 | 3篇 |
1979年 | 5篇 |
1978年 | 6篇 |
1977年 | 5篇 |
1976年 | 2篇 |
1974年 | 2篇 |
1935年 | 4篇 |
排序方式: 共有954条查询结果,搜索用时 10 毫秒
91.
F T Tseng J N D Gupta E F StaffordJr 《The Journal of the Operational Research Society》2006,57(5):541-551
This paper considers the permutation flowshop scheduling problem with sequence-dependent set-up times and develops a penalty-based heuristic algorithm to find an approximately minimum makespan schedule. The proposed algorithm determines the penalty in time associated with a particular sequence and selects the sequence with the minimum time penalty as the best heuristic solution. Computational results comparing the effectiveness and efficiency of the proposed penalty-based heuristic algorithm with an existing savings index heuristic algorithm are reported and discussed. 相似文献
92.
J. H. Chao H. P. Lee C. L. Tseng C. Y. Chen Y. Y. Wei 《Journal of Radioanalytical and Nuclear Chemistry》2002,254(3):577-581
Evaluation of minimal detectable amounts (MDA) of iodine in various or specified irradiation and measurement conditions is described. Interfering contributions due to Na and Cl to the spectral background as well as the dead time of detection system were calculated in details based on an experimental approach. The MDA of iodine for some important biological samples with various Na and Cl concentrations can be evaluated and predicted according to the specified irradiation and measurement arrangements to meet the requirement of analytical purposes. 相似文献
93.
Matrix-assisted laser desorption/ionization (MALDI) mass spectrometry has the potential to become a valuable tool for the compositional analysis of copolymers. For a copolymer composed of structurally very similar building blocks with minor chain length changes, one would expect the relative peak intensities observed in the MALDI mass spectra to reflect its composition, at least within a narrow mass range. However, we show that variations in experimental conditions in MALDI can have a significant effect on the mass spectral appearance of a copolymer. The effects of concentration, laser power, type of matrices and solvents on mass spectra of an ethylene oxide/propylene oxide copolymer are illustrated. These somewhat surprising results show that great care needs to be exercised when interpreting copolymer spectra for compositional analysis, even for copolymers with structurally similar monomers. This work also points out that further studies are needed to better understand and optimize spectral acquisition conditions for reliable copolymer compositional analysis by MALDI. 相似文献
94.
An ordinary plating solution for indium hexacyanoferrate (InHCF) thin film deposition, mainly composed of equal concentrations
of In3+ and [Fe(CN)6]3–, usually forms precipitates rapidly when either concentration is higher than few millimolar. This contributes to the plating
solution's instability. Moreover, electrodeposited capacities are limited accordingly. In this work, the plating solution's
stability and the electrodeposition of InHCF were greatly enhanced by adding a large amount of K+ and/or H+. It was found that a 10-mM plating solution added with 1 M HCl and 1 M KCl could be stored as fresh over a one-week period,
whereas an unmodified plating solution became useless within a couple of minutes. Also, such cationic additions, especially
adding H+, increased the electrodeposited capacity ca. 18 times at least, as compared with that obtained from the unmodified plating
solution. Furthermore, related enhancing mechanisms were proposed and verified. To sum up, this study offers a means for better
InHCF electrodeposition and should promote the applications of InHCF films.
Electronic Publication 相似文献
95.
Ming‐Han Liu Yao‐Hung Tseng Heather F. Greer Prof. Dr. Wuzong Zhou Prof. Dr. Chung‐Yuan Mou 《Chemistry (Weinheim an der Bergstrasse, Germany)》2012,18(50):16104-16113
Mesocrystals of ZnO were synthesized hydrothermally by using gum arabic as a structure‐directing agent. Their hierarchical structure has a unique twin‐brush form consisting of vertically aligned nanorods in a single‐crystal‐like porous form. The formation mechanism of the twin‐brush ZnO was investigated by quenching a series of samples at different times and examining them by TEM, SEM, and XRD. The alignment of ZnO crystal units can be modulated by adding simple salts such as KCl to change the units from nanorods to nanoplates. This can be explained by screening the dipolar force of the polar crystal. Local cathodoluminescence of twin‐brush ZnO was used to follow the local structure changes. 相似文献
96.
The performance of conventional and low-flow nebulizer systems with liquid chromatography in differentiating four arsenic species in urine was evaluated. Two low-flow (DIN and MCN) chamber assemblies and a conventional (CFN) nebulizer-spray chamber assembly were compared in the hyphenation of anion-exchange microbore liquid chromatography with inductively coupled plasma mass spectrometry. Under optimal analytical conditions, the detection limits of the four arsenic species were 0.2-0.6 ng ml(-1) for all the nebulizer systems tested. The chromatographic resolution was best in the case of DIN due to its minimal off-column dead volume and superior transport efficiency. Four arsenic species were determined in the certified reference materials NIST SRM 2670E and 2670N. 相似文献
97.
98.
You-Im Chang Wei-You Cheng Hui-Jen Tseng Keng-Yi Liao 《Colloid and polymer science》2012,290(9):801-816
New correlation equations for the deep-bed filtration, including the term of diffusiophoresis, in addition to the Derjaguin and Landau, Verwey and Overbeek interactions, the Brownian diffusion and the interception, for predicting the initial collection efficiency under the favorable deposition condition and the filter coefficient ratio under the unfavorable deposition condition are derived by using the Brownian dynamics-simulation method. These new correlation equations for predicting the filter coefficient ratio are able to describe previous experimental results especially well for those submicron particles that are at high ionic strength. 相似文献
99.
A 6000-fold rate enhancement has been observed for the hydrolysis of bis(p-nitrophenyl)phosphate (BNPP) in the presence of 0.2 mM Cu(i-Pr(3)[9]aneN(3))(2+) at pH 9.2 and 50 degrees C. In a direct comparison, the rate of hydrolysis of BNPP is accelerated at least 60-fold over the previously reported catalyst Cu([9]aneN(3))(2+). As observed for Cu([9]aneN(3))(2+), hydrolysis is selective for diesters over monoesters. Hydrolysis of BNPP by Cu(i-Pr(3)[9]aneN(3))(2+) is catalytic, exhibiting both rate enhancement and turnover. The reaction is inhibited by both p-nitrophenyl phosphate and inorganic phosphate. The reaction is first-order in substrate and half-order in metal complex, with a k(1.5) of 0.060 +/- 0.004 M(-1/2) s(-1) at 50 degrees C. The temperature dependence of the rate constant results in a calculated activation enthalpy (Delta H(++) of 51 +/- 2 kJ mol(-1) and activation entropy (Delta S(++)) of -110 +/- 6 J mol(-1) K(-1). The kinetic pK(a) of 7.8 +/- 0.2 is close to the thermodynamic pK(a) of 7.9 +/- 0.2, consistent with deprotonation of a coordinated water molecule in the active form of the catalyst. The active catalyst [Cu(i-Pr(3)[9]aneN(3))(OH)(OH(2))](+) is in equilibrium with an inactive dimer, and the formation constant for this dimer is between 216 and 1394 M(-1) at pH 9.2 and 50 degrees C. Temperature dependence of the dimer formation constant K(f) indicates an endothermic enthalpy of formation for the dimer of 27 +/- 3 kJ mol(-1). The time course of anaerobic DNA cleavage by Cu(i-Pr(3)[9]aneN(3))(2+) is presented over a wide range of concentrations at pH 7.8 at 50 degrees C. The concentration dependence of DNA cleavage by Cu([9]aneN(3))(2+) and Cu(i-Pr(3)[9]aneN(3))(2+) reveals a maximum cleavage efficiency at sub-micromolar concentrations of cleavage agent. DNA cleavage by Cu(i-Pr(3)[9]aneN(3))(2+) is twice as efficient at pH 7.8 as at pH 7.2. 相似文献
100.
Ballardini R Balzani V Clemente-León M Credi A Gandolfi MT Ishow E Perkins J Stoddart JF Tseng HR Wenger S 《Journal of the American Chemical Society》2002,124(43):12786-12795
We have designed, synthesized, and investigated a self-assembling supramolecular system which mimics, at a molecular level, the function performed by a macroscopic electrical extension cable. The system is made up of three components, 12+, 2-H3+, and 3. Component 12+ consists of two moieties: a [Ru(bpy)3]2+ unit, which plays the role of an electron donor under light excitation, and a DB24C8 crown ether, which fulfills the function of a socket. The wire-type component 2-H3+ is also composed of two moieties, a secondary dialkylammonium-ion center and a bipyridinium unit, which thread into the DB24C8 crown-ether socket of 12+ and the 1/5DN38C10 crown-ether socket 3, respectively. The photochemical, photophysical, and electrochemical properties of the three separated components, of the 12+ superset 2-H3+ and 2-H3+ subset 3 dyads, and of the 12+ superset 2-H3+ subset 3 triad have been investigated in CH2Cl2 solution containing 2% MeCN. Reversible connection/disconnection of the two plug/socket systems can be controlled independently by acid/base and redox stimulation. The behavior of the various different dyads and triad has been monitored by light absorption and emission spectroscopies, as well as by electrochemical techniques. In the fully connected 12+ superset 2-H3+ subset 3 triad, light excitation of the [Ru(bpy)3]2+ unit of component 12+ is followed by electron transfer (k = 2.8 x 108 s-1) to the bipyridinium unit of component 2-H3+, which is plugged into component 3. Possible schemes to obtain improved molecular-level electrical extension cables are discussed. 相似文献