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891.
《先进技术聚合物》2018,29(1):497-506
A novel phosphorus‐containing, nitrogen‐containing, and sulfur‐containing reactive flame retardant (BPD) was successfully synthesized by 1‐pot reaction. The intrinsic flame‐retardant epoxy resins were prepared by blending different content of BPD with diglycidyl ether of bisphenol‐A (DGEBA). Thermal stability, flame‐retardant properties, and combustion behaviors of EP/BPD thermosets were investigated by differential scanning calorimetry (DSC), thermogravimetric analysis (TGA), limited oxygen index (LOI) measurement, UL94 vertical burning test, and cone calorimeter test. The flame‐retardant mechanism of BPD was studied by TGA/infrared spectrometry (TGA‐FTIR), pyrolysis‐gas chromatography/mass spectrometry (Py‐GC/MS), morphology, and chemical component analysis of the char residues. The results demonstrated that EP/BPD thermosets not only exhibited outstanding flame retardancy but also kept high glass transition temperature. EP/BPD‐1.0 thermoset achieved LOI value of 39.1% and UL94 V‐0 rating. In comparison to pure epoxy thermoset, the average of heat release rate (av‐HRR), total heat release (THR), and total smoke release (TSR) of EP/BPD‐1.0 thermoset were decreased by 35.8%, 36.5% and 16.5%, respectively. Although the phosphorus content of EP/BPD‐0.75 thermoset was lower than that of EP/DOPO thermoset, EP/BPD‐0.75 thermoset exhibited better flame retardancy than EP/DOPO thermoset. The significant improvement of flame retardancy of EP/BPD thermosets was ascribed to the blocking effect of phosphorus‐rich intumescent char in condensed phase, and the quenching and diluting effects of abundant phosphorus‐containing free radicals and nitrogen/sulfur‐containing inert gases in gaseous phase. There was flame‐retardant synergism between phosphorus, nitrogen, and sulfur of BPD. 相似文献
892.
Rachel Quarrell Timothy D. W. Claridge George W. Weaver Gordon Lowe 《Molecular diversity》1996,1(4):223-232
Summary In view of the widespread use of TentaGel resin beads for the synthesis of combinatorial libraries, the properties of TentaGel resin have been examined using a combination of confocal laser microscopy and NMR spectroscopy. Evidence is presented that trypsin, a 23.5-kDa enzyme, can penetrate to the core of 90-m TentaGel beads, and that the matrix of such beads permits molecular motion at a similar rate to that in solution. The beads act as a separate gel phase rather than as a porous solid. These conclusions have important implications for the bioassay of on-bead combinatorial chemical libraries. 相似文献
893.
N. N. Ezhova G. A. Korneeva E. V. Slivinsky R. A. Aronovich 《Russian Chemical Bulletin》1995,44(1):69-73
Hydroformylation of formaldehyde to give glycolaldehyde (GA) in the presence of RhCl(PPh3)3, RhCl(CO)(PPh3)2, or the RhCl3 + PPh3 system inN,N-dimethylacetamide was studied. The hydroformylation is accompanied by the Cannizzaro-Tishchenko reaction, condensation of CH2O with GA to give C3-C16 polyoxyaldehydes (POA), and dimerization of GA. The formation of POA, which probably occurs through coordination of GA with a Rh atom, predominates among the side reactions. The optimum conditions for hydroformylation of CH2O were found to be: RhCl3 + PPh3 as the catalyst,T 383 K,
12MPa, [H2O] 1.8 mol L–1, [Rh] 2.5 · 10–3 g-at. L–1, and [CH2O] 0.03 g L–1. At a substrate conversion of 62–67 %, the selectivity of GA formation reaches 96 %, and the yield is 60–65 %.Translated fromIzvestiya Akademii Nauk. Seriya Khimicheskaya, No. 1, pp. 75–78, January, 1995. 相似文献
894.
895.
用芳烷基酚树脂与玻璃纤维布制成纤维增强材料,研究了引材料的高温热老化性能和在30-50%热沸太航热醋和含氯离子的热沸醋酸下的腐蚀性能。 相似文献
896.
N. N. Yarmukhamedov N. Z. Baibulatova V. A Dokichev T. V. Khakimova L. V. Spirikhin Yu. V. Tomilov M. S. Yunusov 《Russian Chemical Bulletin》2005,54(2):414-420
1,5-Dinitro-3,7-diazabicyclo[3.3.1]nonane derivatives were synthesized in up to 83%yields by the Mannich reaction of 1,3-dinitropropanes with excess formaldehyde and primary amines. In some cases, for instance, when 2,2-dimethyl-1,3-dinitropropane and benzylamine or monoethanolamine are used, the reaction occurs with low yields or stops at the step of formation of 3,5-dinitropiperidines. The influence of the structure of the starting compounds and reaction conditions on the yields of 1,5-dinitro-3,7-diazabicyclo[3.3.1]nonanes and 3,5-dinitropiperidines was studied.__________Published in Russian in Izvestiya Akademii Nauk. Seriya Khimicheskaya, No. 2, pp. 405–411, February, 2005. 相似文献
897.
环氧树脂微粒化水基化体系 总被引:25,自引:0,他引:25
本文系统介绍了环氧树脂微粒化水基化体系的特点及用途,制备方法和反映体系特性的一些重要参数。 相似文献
898.
Thermodynamic characteristics of adsorption of organic compounds on semiinterpenetrating networks based on polybenzimidazoles and polyaminoimide resin with different compositions were studied at small coverages using inverse gas chromatography. The following characteristics were determined: adsorption equilibrium constants (specific retention volumes) of substances of different classes (n-alkanes, aromatic hydrocarbons, ethers, ketones, alcohols, and nitrogen- and halogen-containing compounds), appropriate changes in differential molar internal energy and Helmholtz potential, and changes in standard molar entropy of the sorbates. The contributions of the molecular fragments to the heat of adsorption were calculated. The adsorption properties of the semiinterpenetrating networks based on polybenzimidazoles and polyaminoimide resin differ from those of the starting polymeric materials and their physical mixtures with the similar composition. Unlike graphitized thermal carbon black (nonspecific adsorbent), the network and starting materials manifest the specific properties (electron-donating and electron-accepting). The difference in the thermodynamic characteristics of adsorption on the semiinterpenetrating polymeric networks with different compositions is determined by the size and geometry of interphase regions. 相似文献
899.
Acid treatment for functionalizing polyethylene fiber surfaces for enhanced adhesion to epoxy resins
The utility of high-strength, high-modulus polyethylene fibers in fiber-reinforced composites is limited due to its poor interfacial adhesion to various polymeric matrices. One way to overcome this limitation is to introduce reactive functionalities on the fiber surface capable of covalently bonding to matrix resins. Ultra high-strength polyethylene (UHSPE) fibers were treated with chlorosulfonic acid. The surface acid groups were found to considerably improve the interfacial adhesion between polyethylene fibers and epoxy resins as shown by the microbond test. These surface functionalities were found to improve the fiber wettability, as shown by contact angle measurements using the Wilhelmy balance method. Colorimetric measurements of methylene blue absorption were used to quantify the surface concentrations of the acid groups. It was possible to functionalize the UHSPE fiber surfaces using this method to obtain fibers that formed a stronger adhesive bond with epoxy resins; this was achievable without sacrificing other fiber mechanical properties. 相似文献
900.