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排序方式: 共有602条查询结果,搜索用时 31 毫秒
1.
Rizwan Ahmad Niyaz Ahmad Fatimah AlOthman Haya Mohammad Fatimah AlZahrani 《Biomedical chromatography : BMC》2020,34(1):e4712
Coffee and tea are the most widely consumed beverages worldwide. However, the consumer may be unaware of the exact amount of methyl xanthine (MX, i.e. caffeine [C], theobromine [TB] and theophylline [TH]) consumed, as most of the products do not list the proper amounts. This may lead to serious risks including cardiovascular, kidney and stimulant effects. The aim of the study was to determine the MX amount in ready-to-use beverages (coffee and tea) collected from various outlets in the city of Al-Khobar, Saudi Arabia. Forty different samples of espresso, black coffee and red tea were collected. A fast, reliable and efficient UHPLC–DAD method was developed and validated for MX determination. Total lipids were extracted and fractionated in order to determine glycolipids, phospholipids and neutral lipids. The r2 value for the method was 0.980–0.988 in a linearity range of 0.5–200 ppm. The range for MX (C [0.02–2.39 mg/ml], TB [0.00–0.10 mg/ml] and TH [0.00–0.004 mg/ml]) and total lipids was 1–5 g. The amount of glycolipids (3.1 g) was higher among the lipid fractions followed by phospholipids (1.8 g) and neutral lipids (0.25 g). In general, espresso beverages (20–30 ml) contained high amounts of MX whereas black coffee beverages contained high amount of lipids. Most of the beverages expressed C, TB, TH, lipids or their fractions; however, the product with high amounts of MX and lipids at the same time was espresso (brands Chemistry and Wogard). Although the MX and lipid levels in these beverages well below the allowed limits, care must still be taken, especially when using the beverages with high serving volumes (200–250 ml) or coffee prepared via the filter method i.e. black coffee, using a high temperature for a longer time. 相似文献
2.
Yu. F. Dolgii E. V. Ul’yanov 《Proceedings of the Steklov Institute of Mathematics》2007,259(2):S95-S110
To obtain sufficient conditions for the asymptotic stability of linear periodic systems with fixed delay commensurable with the period of coefficients, singular numbers of the monodromy operator are used. To find these numbers, a self-adjoint boundary value problem for ordinary differential equations is applied. We study the motion of eigenvalues of this boundary value problem under a variation of a parameter. Obtaining sufficient conditions for the asymptotic stability is reduced to finding the bifurcation value of the parameter for the boundary value problem. 相似文献
3.
O. V. Okatova N. N. Ul’yanova E. G. Bulycheva L. B. Elshina A. L. Rusanov P. N. Lavrenko 《Polymer Science Series A》2007,49(6):716-721
The molecular properties of a number of new poly(naphthylimides) derived from naphthalene-1,4,5,8-tetracarboxylic dianhydride and bis(naphthalic anhydrides) have been studied. On the basis of hydrodynamic studies of the polymers at various stages of their thermal degradation in 96% H2SO4 and thermogravimetric measurements, the hydrolytic stability and thermooxidative resistance of the polymers have been compared. A correlation between the experimental data and the chemical structure of molecular chains has been established. 相似文献
4.
Humblot V Lorenzo MO Baddeley CJ Haq S Raval R 《Journal of the American Chemical Society》2004,126(20):6460-6469
A detailed comparison of tartaric acid (HOOC-CHOH-CHOH-COOH) and succinic acid (HOOC-CH(2)-CH(2)-COOH) molecules on a Cu(110) surface is presented with a view to elucidate how the two-dimensional chirality exhibited by such robust, chemisorbed systems is affected when both OH groups of the former molecule are replaced with H groups, a stereochemical change that leaves the metal-bonding functionalities of the molecule untouched but destroys both chiral centers. It is found that this change does not significantly affect the thermodynamically preferred chemical forms that are adopted, namely the doubly deprotonated bicarboxylate at low coverages (theta = (1)/(6) ML) and the singly deprotonated monocarboxylate at higher coverage. However, the kinetics of phase formation are significantly affected so that the conditions required for self-assembling pertinent two-dimensional chiral phases alter substantially. For both molecules, two-dimensional assembly is found to depend strongly on the nature of the local adsorption motif created, with each motif essentially acting as a "synthon" for the supramolecular assembly. In this respect, it seems that molecule-metal bonding interactions define the general self-assembly structure. The presence/absence of the OH groups, instead, cause a subtler, second-order effect on the finer details of the self-assembled structure. Finally, the creation of chirality in the achiral succinate system is shown to arise from adsorption-induced asymmetrization, inducing point chirality via molecular distortion and/or metal reconstruction of the local adsorption unit. This chiral adsorption unit is then responsible for creating chiral supramolecular through-space and through-metal interactions that propagate a chiral organization. However, the achirality of the succinate ensures that nucleation points of either chirality are equally created, producing a racemic conglomerate of coexisting mirror domains. It is in this aspect that the uniquely aligned OH groups of the rigid bitartrate system wield the greatest effect, by favoring one distortion/reconstruction for the (R,R)-bitartrate and its mirror image distortion/reconstruction for the (S,S)-enantiomer, creating surfaces that are globally chiral on the macroscopic scale. So overall, the OH groups do not dictate the general nature of the assembly but are critical as chiral propagators, breaking the degeneracy and thus promoting asymmetry to chirality. 相似文献
5.
When water is adsorbed on Pt(111) above 135 K several different ice structures crystallize, depending on the thickness of the ice layer. At low coverage water forms extended islands of ice with a (square root(37) x square root(37))R25(o) unit cell, which compresses as the monolayer saturates to form a (square root(39) x square root(39))R16(o) structure. The square root(39) low-energy electron diffraction (LEED) pattern becomes more intense as the second layer grows, remaining bright for films up of 10-15 layers and then fading and disappearing for films more than ca. 40 layers thick. The ice multilayer consists of an ordered square root(39) wetting layer, on which ice grows as a crystalline film which progressively loses its registry to the wetting layer. Ice films more than ca. 50 layers thick develop a hexagonal LEED pattern, the entire film and wetting layer reorienting to form an incommensurate bulk ice. These changes are reflected in the vibrational spectra which show changes in line shape and intensity associated with the different ice structures. Thin amorphous solid water films crystallize to form the same phases observed during growth, implying that these structures are thermodynamically stable and not kinetic phases formed during growth. The change from a square root(39) registry to incommensurate bulk ice at ca. 50 layers is associated with a change in crystallization kinetics from nucleation at the Pt(111) interface in thin films to nucleation of incommensurate bulk ice in amorphous solid water films more than 50 layers thick. 相似文献
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8.
Yu. M. Samchenko I. D. Atamanenko T. P. Poltoratskaya Z. R. Ul’berg 《Colloid Journal》2006,68(5):613-616
The sorption capacity (upon water sorption from the bulk and vapor phases) of copolymeric hydrogels based on acrylamide and acrylic acid and the state of water in the hydrogels are studied. It is established that, for hydrogels prepared in the form of fine powders, pore sizes vary from 90 to 770 Å and the pore radius of hydrogels obtained as monolithic plates ranges from 27 to 200 Å. The acrylamide-to-acrylic acid unit ratio in the hydrogels is found to affect both the amount and the state of sorbed water. It is shown that the properties of water sorbed by hydrogels are governed by carboxyl group concentration rather than by the density of macromolecular chains. 相似文献
9.
The influence of various reclamation agents (montmorillonite, peat, activated sludge microbocenosis) on the stability of dispersions of the colloidal fraction of meadow chernozem soil is studied. It is established that biocolloids possess the strongest coagulating action in the aforementioned series of reclamation agents. It is shown that, in the process of microorganism growth involving glucose or polypeptides as a carbon source, exopolymers are synthesized that caused the coagulation of soil dispersions. Upon the growth of microorganisms on polypeptides (alkaligeneous metabolism), precipitates are formed that are denser and less peptized by water than those grown on glucose (acidogeneous metabolism). The addition of montmorillonite and peat intensifies the aggregation processes in soil-microbe heterodispersions. The inverse relationship between the content of an organic substance in a colloidal system and the stability of aggregates of soil colloids is revealed. 相似文献
10.