全文获取类型
收费全文 | 1089篇 |
免费 | 20篇 |
国内免费 | 4篇 |
专业分类
化学 | 595篇 |
晶体学 | 12篇 |
力学 | 59篇 |
数学 | 60篇 |
物理学 | 387篇 |
出版年
2022年 | 18篇 |
2021年 | 15篇 |
2020年 | 26篇 |
2019年 | 14篇 |
2018年 | 22篇 |
2017年 | 27篇 |
2016年 | 30篇 |
2015年 | 18篇 |
2014年 | 21篇 |
2013年 | 79篇 |
2012年 | 45篇 |
2011年 | 57篇 |
2010年 | 36篇 |
2009年 | 39篇 |
2008年 | 53篇 |
2007年 | 47篇 |
2006年 | 59篇 |
2005年 | 41篇 |
2004年 | 43篇 |
2003年 | 27篇 |
2002年 | 33篇 |
2001年 | 14篇 |
2000年 | 22篇 |
1999年 | 9篇 |
1998年 | 9篇 |
1997年 | 6篇 |
1996年 | 7篇 |
1995年 | 7篇 |
1994年 | 14篇 |
1993年 | 15篇 |
1992年 | 9篇 |
1991年 | 15篇 |
1990年 | 11篇 |
1989年 | 10篇 |
1988年 | 10篇 |
1987年 | 6篇 |
1986年 | 8篇 |
1985年 | 14篇 |
1984年 | 18篇 |
1983年 | 8篇 |
1982年 | 16篇 |
1981年 | 16篇 |
1980年 | 12篇 |
1979年 | 13篇 |
1978年 | 14篇 |
1977年 | 12篇 |
1976年 | 14篇 |
1973年 | 16篇 |
1972年 | 4篇 |
1956年 | 7篇 |
排序方式: 共有1113条查询结果,搜索用时 15 毫秒
1.
The spin-1 Ising model, which is equivalent to the three-component lattice gas model, is used to study wetting transitions in three-component surfactant systems consisting of an oil, water, and a nonionic surfactant. Phase equilibria, interfacial profiles, and interfacial tensions for three-phase equilibrium are determined in mean field approximation, for a wide range of temperature and interaction parameters. Surfactant interaction parameters are found to strongly influence interfacial tensions, reducing them in some cases to ultralow values. Interfacial tensions are used to determine whether the middle phase, rich in surfactant, wets or does not wet the interface between the oil-rich and water-rich phases. By varying temperature and interaction parameters, a wetting transition is located and found to be of the first order. Comparison is made with recent experimental results on wetting transitions in ternary surfactant systems.This paper is dedicated to J. K. Percus in honor of his 65th birthday. 相似文献
2.
3.
We have initiated a search for a new type of nuclear matter, theη-mesic nucleus, using beams from the multi-GeV hadron facility, COSY at Juelich, Germany. A large acceptance scintillator detector, ENSTAR has been designed and built at BARC, Mumbai and fully assembled and tested at COSY. A test run for calibration and evaluation has been completed. In this contribution we present the design and technical details of the ENSTAR detector and how it will be used to detect protons and pions (the decay products ofη-mesic bound state). The detector is made of plastic scintillators arranged in three concentric cylindrical layers. The readout of the detectors is by means of optical fibres. The layers are used to generate ΔE –E spectra for particle identification and total energy information of stopped particles. The granularity of the detector allows for position (θ and ?ø determination making the event reconstruction kinematically complete 相似文献
4.
5.
J. S. Shukla R. K. Tiwari 《Journal of polymer science. Part A, Polymer chemistry》1981,19(6):1517-1524
The aqueous polymerization of methacrylamide (I) initiated by KBrO3–thioglycolic acid (TGA) has been studied at 30 ± 0.2°C in nitrogen. The rate is given by K[M]1.19 [thioglycolic acid]1 [KBrO3]0.53 for 10–15% conversion. Activation energy was found to be 53.96 kJ/mole (12.92 kcal/mole) in the investigated range of temperature 30–45°C. The role of addition of a series of aliphatic alcohols and some salts was also determined. The kinetics of polymerization was followed iodometrically. 相似文献
6.
A. K. Shukla S. Saini P. Kumar J. S. P. Rai A. K. Srivastava 《Journal of polymer science. Part A, Polymer chemistry》1989,27(3):807-815
Polymerization of vinyl acetate initiated by β-picolinium p-chlorophenacylide was carried out at 30, 35, and 40°C, using conventional dilatometric technique. The initiator and the monomer exponent values were 0.80 ± 0.15 and unity, respectively. The polymerization was inhibited in the presence of hydroquinone, but was favored by nonpolar solvent and polymerization temperature. The energy of activation was 90.3 KJ mol?1. An average value of k/kt for the present system was found to be 0.37 × 10?2. The results are explained in terms of a radical mode of polymerization with degradative initiator transfer; the principal mode of termination, however, was bimolecular. 相似文献
7.
Shukla AK 《European journal of mass spectrometry (Chichester, England)》2004,10(2):221-224
We have measured relative abundances of fragment ions resulting from collision-induced dissociation of OCS(+) ions in collision with xenon neutrals as a function of ion kinetic energy and scattering angle. The lowest energy dissociation product, S(+), dominates at all energies up to 53 eV kinetic energy studied here. Surprisingly, the second most abundant dissociation channel is CS(+) and not CO(+) even though the thermochemical threshold for CO(+) is lower than that for CS(+) and CO(+) is more abundant than CS(+) in the normal mass spectrum of OCS. We do not observe any significant abundance of CO(+) in this energy range, suggesting that collision-induced excitation and dissociation of OCS(+) is significantly different to that of symmetric triatomic ions. A possible role of asymmetry in the molecular ion's collisional activation via neutral collision is suggested for the different behavior. 相似文献
8.
The association of many classes of surface-active molecules into micellar aggregates is a well-known phenomenon. Micelles are in dynamic equilibrium, constantly disintegrating and reforming. This relaxation process is characterized by the slow micellar relaxation time constant, tau(2), which is directly related to the micellar stability. Theories of the kinetics of micelle formation and disintegration have been discussed to identify the gaps in our complete understanding of this kinetic process. The micellar stability of sodium dodecyl sulfate micelles has been shown to significantly influence technological processes involving a rapid increase in interfacial area, such as foaming, wetting, emulsification, solubilization, and detergency. First, the available monomers adsorb onto the freshly created interface. Then, additional monomers must be provided by the breakup of micelles. Especially when the free monomer concentration is low, which is the case for many nonionic surfactant solutions, the micellar breakup time is a rate-limiting step in the supply of monomers. The Center for Surface Science & Engineering at the University of Florida has developed methods using stopped flow and pressure jump with optical detection to determine the slow relaxation time of micelles of nonionic surfactants. The results showed that the ionic surfactants such as SDS exhibit slow relaxation times in the range from milliseconds to seconds, whereas nonionic surfactants exhibit slow relaxation times in the range from seconds (for Triton X-100) to minutes (for polyoxyethylene alkyl ethers). The slow relaxation times are much longer for nonionic surfactants than for ionic surfactants, because of the absence of ionic repulsion between the head groups. The observed relaxation times showed a direct correlation with dynamic surface tension and foaming experiments. In conclusion, relaxation time data of surfactant solutions correlate with the dynamic properties of the micellar solutions. Moreover, the results suggest that appropriate micelles with specific stability or tau(2) can be designed by controlling the surfactant structure, concentration, and physicochemical conditions (e.g., salt concentration, temperature, and pressure). One can also tailor micelles by mixing anionic/cationic or ionic/nonionic surfactants for a desired stability to control various technological processes. 相似文献
9.
J. S. Shukla P. K. Misra 《Journal of polymer science. Part A, Polymer chemistry》1984,22(11):3401-3405
Novel polyhydrazides having inherent viscosities in the range of 0.24–0.38 dL g?1 were prepared by polymerizing a series of hydrazides with different diacid chlorides in polar aprotic solvents. These polymers display a wide range of solubility in a number of solvents. They start decomposing at about 200°C in air. Results of differential thermal and thermogravimetric analysis show that a steep weight loss takes place mainly in the range of 300–440°C. 相似文献
10.
Binil Itty Ipe Anuj Shukla Huachang Lu Bo Zou Heinz Rehage Christof M Niemeyer 《Chemphyschem》2006,7(5):1112-1118
Currently, there is great interest in the development of methods suitable for determining the stoichiometry of biomolecules attached to nanoparticles. We describe the use of the dynamic light-scattering technique (DLS) to determine the stoichiometry of the protein cytochrome P450(BSbeta) attached to CdS and CdSe quantum dots (QDs). The enzyme-conjugated QDs have different diffusion characteristics compared to the QD and enzyme precursors, expressed in their size, scattering intensity as well as zeta-potential values. The significant enhancement of the scattering intensity of QDs observed upon conjugation with the P450(BSbeta) due to the refractive-index increment and the systematic variation in zeta potential resulting from charge neutralization of the anionic QDs by the cationic histidine-tagged P450(BSbeta) have been used for stoichiometry determination. 相似文献