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91.
Yuri M. Boiko Dmitri V. Lebedev Liubov P. Myasnikova 《Colloid and polymer science》2013,291(6):1519-1523
The isothermal luminescence decay kinetics in near-surface nanolayers of plasma-activated bulk samples of amorphous polystyrene (PS) and poly(2,6-dimethyl-1,4-phenylene oxide) (PPO) and their miscible blends with weight ratios PS/PPO of 75/25 and 50/50 has been studied at 77 K. The intensities of isothermal luminescence (I) of homopolymer and blend surfaces have been compared. It has been found that the ratio between the luminescence intensities for PS and PPO (I(PS)/I(PPO)) may be as high as 50, while the luminescence intensities for the PS–PPO blends are close to I(PPO). The results obtained indicate that the PPO concentration in the surface layers of the blends is higher than that in the bulk. 相似文献
92.
Yuri?E.?GliklikhEmail author Olga?O.?Zheltikova 《Methodology and Computing in Applied Probability》2015,17(1):91-105
The paper is devoted to a brief introduction into the theory of equations and inclusions with mean derivatives and to investigation of a special type of such inclusions called inclusions of geometric Brownian motion type. The existence of optimal solutions maximizing some cost criteria, is proved. 相似文献
93.
94.
Physicochemical and adsorption properties of hypercross‐linked polystyrene with ultimate cross‐linking density 下载免费PDF全文
Maria P. Tsyurupa Zinaida K. Blinnikova Yuri A. Borisov Mikhail M. Ilyin Tamara P. Klimova Kiril V. Mitsen Vadim A. Davankov 《Journal of separation science》2014,37(7):803-810
The paper describes unexpected properties of hypercross‐linked polystyrenes with ultimate cross‐linking degrees of 300, 400, and 500%, where three, four, or five methylene links, respectively, could bind each polystyrene phenyl ring to its spacious neighbors. The polymers exhibit a strong electron spin resonance signal, unusual spectra in IR, UV, and visible ranges, and they are not typical dielectrics. The nonfunctionalized hypercross‐linked polymers absorb significant amounts of inorganic acids, salts, and bases due to interactions of protons or other cations with electron‐donating fragments of the aromatic network with the high extent of mutual connectivity and also due to dispersion interactions of anions with the polymer matrix. 相似文献
95.
96.
Neshev DN Sukhorukov AA Dreischuh A Fischer R Ha S Bolger J Bui L Krolikowski W Eggleton BJ Mitchell A Austin MW Kivshar YS 《Physical review letters》2007,99(12):123901
We present the first observation of spatiospectral control and localization of supercontinuum light through the nonlinear interaction of spectral components in extended periodic structures. We use an array of optical waveguides in a LiNbO3 crystal and employ the interplay between diffraction and nonlinearity to dynamically control the output spectrum of the supercontinuum radiation. This effect presents an efficient scheme for optically tunable spectral filtering of supercontinua. 相似文献
97.
Concentration dependence of nonlinear refractive index n2 in fibers heavily doped with GeO2 is studied by using the D-scan method. Good agreement with an empirical dependence established earlier with lower GeO2 concentrations by the cw dual-frequency beat signal technique is shown for GeO2 concentrations up to approximately 100 mol.%. The highest values of the nonlinear coefficient gamma at 1.25 microm of 47.9, 57.7, and 70.9 W(-1) km(-1) were obtained in fibers doped with 67, 75, and 97 mol.% GeO2, respectively. 相似文献
98.
Efficient Biocatalytic Degradation of Pollutants by Enzyme‐Releasing Self‐Propelled Motors 下载免费PDF全文
Dr. Jahir Orozco Diana Vilela Dr. Gabriela Valdés‐Ramírez Yuri Fedorak Prof. Alberto Escarpa Prof. Rafael Vazquez‐Duhalt Prof. Joseph Wang 《Chemistry (Weinheim an der Bergstrasse, Germany)》2014,20(10):2866-2871
The first example of a self‐propelled tubular motor that releases an enzyme for the efficient biocatalytic degradation of chemical pollutants is demonstrated. How the motors are self‐propelled by the Marangoni effect, involving simultaneous release of SDS surfactant and the enzyme remediation agent (laccase) in the polluted sample, is illustrated. The movement induces fluid convection and leads to the rapid dispersion of laccase into the contaminated solution and to a dramatically accelerated biocatalytic decontamination process. The greatly improved degradation efficiency, compared to quiescent solutions containing excess levels of the free enzyme, is illustrated for the efficient biocatalytic degradation of phenolic and azo‐type pollutants. The high efficiency of the motor‐based decontamination approach makes it extremely attractive for a wide‐range of remediation processes in the environmental, defense and public health fields. 相似文献
99.
Sai Venkatesh Pingali Hugh M. O’Neill Yoshiharu Nishiyama Lilin He Yuri B. Melnichenko Volker Urban Loukas Petridis Brian Davison Paul Langan 《Cellulose (London, England)》2014,21(2):873-878
Morphological changes to the different components of lignocellulosic biomass were observed as they occurred during steam pretreatment by placing a pressure reaction cell in a neutron beam and collecting time-resolved neutron scattering data. Changes to cellulose morphology occurred mainly in the heating phase, whereas changes in lignin morphology occurred mainly in the holding and cooling phases. During the heating stage, water is irreversibly expelled from cellulose microfibrils as the elementary fibrils coalesce. During the holding phase lignin aggregates begin to appear and they increase in size most noticeably during the cooling phase. This experiment demonstrates the unique information that in situ small angle neutron scattering studies of pretreatment can provide. This approach could be useful in optimizing the heating, holding and cooling stages of pretreatments to allow the exact size and nature of lignin aggregates to be controlled in order to enhance enzyme accessibility to cellulose and therefore the efficiency of biomass conversion. 相似文献
100.
Yuri Feldman Alexander Puzenko Paul Ben Ishai Anna Gutina Greenbaum 《Colloid and polymer science》2014,292(8):1923-1932
Water is the universal solvent in nature. Does this imply, however, that its interaction with its environment is also a universal feature? While this question maybe too fundamental to be answered by one method only, we present evidence that the broadening of the dielectric spectra of water presents universal features of dipolar interactions with different types of matrixes. If in aqueous solutions the starting point of water’s state can be considered as bulk, with only partial interactions with the solute, then the state of water adsorbed in heterogeneous materials is determined by various hydration centers of the inhomogeneous material (the matrix) and it is significantly different from the bulk. In both cases, the dielectric spectrum of water is symmetrical and can be described by the Cole–Cole (CC) function. The phenomenological model that describes a physical mechanism of the dipole–matrix interaction in complex systems underlying the CC behavior has been applied to water adsorbed in porous glasses. It was then extended to analyses of the dynamic and structural behavior of water in nonionic and ionic aqueous solutions. The same model is then used to analyze the CC relaxation processes observed in clays, aqueous solutions of nucleotides, and amino acids. 相似文献