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111.
Second-derivative synchronous fluorescence spectrometry was used to develop a simple, rapid and sensitive spectrofluorimetric method for the determination of binary mixtures of the nonsteroidal antiinflammatory drugs flufenamic (FFA), meclofenamic (MCFA) and mefenamic (MFA) acids in serum and pharmaceutical formulations. The method is based on the intrinsic fluorescence of these compounds in chloroform. A Deltalambda=105 nm was used for the resolution of FFA-MFA and MFA-MCFA mixtures, whereas the FFA-MCFA mixture was determined at Deltalambda=40 nm. Serum samples are treated with trichloroacetic acid to remove the proteins, and the analytes are extracted in chloroform prior to determination. Pharmaceutical preparations were analysed without prior separation steps. 相似文献
112.
Kinetics of the hydrolysis of bisphenol A diglycidyl ether (BADGE) in water-based food simulants 总被引:1,自引:0,他引:1
P. Paseiro Losada J. Simal Lozano S. Paz Abuín P. López Mahía J. Simal Gándara 《Fresenius' Journal of Analytical Chemistry》1993,345(7):527-532
Summary The first-order degradation kinetics of bisphenol A diglycidyl ether (BADGE; CAS No. 1675-54-3) has been studied in three water-based food simulants (3% (W/V) acetic acid, distilled water and 15% (V/V) ethanol) at various temperatures. BADGE and its first and second hydrolysis products were determined by reversed-phase high-performance liquid chromatography with fluorescence detection. Nonlinear regression was used to fit the experimental data at 40, 50 and 60°C with the proposed kinetic equations; Arrhenius' equation was then fitted to the rate constants obtained and the kinetic models were tested by comparing experimental data obtained at 70°C with the kinetic curves calculated using the rate constants predicted for this temperature. The half-life of BADGE was longest in ethanol and shortest in acetic acid. The rings opening in acetic acid appears to happen by means of active hydrogens whereas in the other simulants it is mainly influenced by the formation of acid/base adducts. The results imply that resins which comply with existing legislation on the migration of unreacted monomer may still contaminate foodstuffs. 相似文献
113.
Supercritical fluid extraction was applied to the determination of naturally contaminated polycyclic aromatic hydrocarbons (PAHs) in bird tissue by liquid chromatography with fluorescence detection (LC-FL). Recoveries (> 90%) and relative standard deviations (< or = 7.7%) were satisfactory. The levels of 10 PAHs were analyzed in 6 classes of tissues (heart, liver, intestine, muscle, lung, and kidney) of 10 buzzards and 2 tawny owls, predatory birds from the Galicia (northwest Spain). The PAHs found most abundantly were pyrene, fluoranthene, benzo[a]anthracene, and anthracene. Chrysene, benzo[b]fluoranthene, benzo[k]fluoranthene, benzo[ghi]perylene, and indeno[1,2,3-cd]pyrene were not detected. Intestine, kidney, and lung were more polluted than other tissues. 相似文献
114.
Carlos Elvira Angel E. Lozano Julio San Romn 《Journal of polymer science. Part A, Polymer chemistry》1999,37(24):4528-4535
The kinetic behavior of the free-radical polymerization of 2-hydroxy-4-N-methacrylamidobenzoic acid (4-HMA) and 2-hydroxy-5-N-methacrylamidobenzoic acid (5-HMA) in a solution of N,N-dimethylformamide is described. The methacrylic monomers 4-HMA and 5-HMA were isomers in which the phenolic and carboxylic functional groups were in different positions on the side aromatic ring with respect to the methacrylamide group. Semiempirical (AM1 and PM3 treatments) and ab initio (6-31G**) quantum mechanical calculations indicated the existence of intramolecular H-bonding between the phenolic and carboxylic groups. These calculations also indicated a slightly higher reactivity of 4-HMA with respect to 5-HMA under the same experimental conditions as obtained from the frontier orbital interactions between the highest molecular orbital of the monomers and the singly occupied molecular orbital of the radical obtained by the reaction of a methyl radical with the corresponding monomer. Gravimetric study of the free-radical polymerization of 4-HMA and 5-HMA at several temperatures ranging from 50 to 150 °C demonstrated this behavior. The kinetic results obtained and the average molecular weights of the polymers prepared at different temperatures indicated that the monomer 4-HMA had a slightly higher reactivity at low temperatures (50–90 °C), whereas at higher temperatures (120–150 °C), the reactivity of both monomers became similar as a consequence of the “dead-end” radical polymerization. © 1999 John Wiley & Sons, Inc. J Polym Sci A: Polym Chem 37: 4528–4535, 1999 相似文献
115.
116.
Lucía Castro-Vzquez María Victoria Lozano Virginia Rodríguez-Robledo Joaquín Gonzlez-Fuentes Pilar Marcos Noemí Villaseca Maria Mar Arroyo-Jimnez Manuel J. Santander-Ortega 《Molecules (Basel, Switzerland)》2021,26(19)
Orange peel by-products generated in the food industry are an important source of value-added compounds that can be potentially reused. In the current research, the effect of oven-drying (50–70 °C) and freeze-drying on the bioactive compounds and antioxidant potential from Navelina, Salustriana, and Sanguina peel waste was investigated using pressurized extraction (ASE). Sixty volatile components were identified by ASE-GC-MS. The levels of terpene derivatives (sesquitenenes, alcohols, aldehydes, hydrocarbons, and esters) remained practically unaffected among fresh and freeze-dried orange peels, whereas drying at 70 °C caused significative decreases in Navelina, Salustriana, and Sanguina peels. Hesperidin and narirutin were the main flavonoids quantified by HPLC-MS. Freeze-dried Sanguina peels showed the highest levels of total-polyphenols (113.3 mg GAE·g−1), total flavonoids (39.0 mg QE·g−1), outstanding values of hesperedin (187.6 µg·g−1), phenol acids (16.54 mg·g−1 DW), and the greatest antioxidant values (DPPH•, FRAP, and ABTS•+ assays) in comparison with oven-dried samples and the other varieties. Nanotechnology approaches allowed the formulation of antioxidant-loaded nanoemulsions, stabilized with lecithin, starting from orange peel extracts. Those provided 70–80% of protection against oxidative UV-radiation, also decreasing the ROS levels into the Caco-2 cells. Overall, pressurized extracts from freeze-drying orange peel can be considered a good source of natural antioxidants that could be exploited in food applications for the development of new products of commercial interest. 相似文献
117.
S Lozano B Adenso-Díaz I Eguia L Onieva 《The Journal of the Operational Research Society》1999,50(5):509-516
As part of the cellular manufacturing design process, machines must be grouped in cells and the corresponding part families must be assigned. Limits on both the number of machines per cell and the number of parts per family can be considered. A weighted sum of intracell voids and intercellular moves is used to evaluate the quality of the solutions. We present a tabu search algorithm that systematically explores feasible machine cells configurations determining the corresponding part families using a linear network flow model. The performance of this tabu search is benchmarked against two simulated annealing approaches, another tabu search approach and three heuristics: (ZODIAC, GRAFICS and MST). 相似文献
118.
Vernica Caldern Flix García Jos L. De la Pea Eva M. Maya ngel E. Lozano Jos G. de la Campa Javier de Abajo Jos Miguel García 《Journal of polymer science. Part A, Polymer chemistry》2006,44(13):4063-4075
This article describes the synthesis and characterization of two diacid monomers, each containing a benzo‐15‐crown‐5 subunit or its dipodal counterpart. Both novel monomers were reacted with technical aromatic diamines with Yamazaki's direct polyamidation method to render modified polyisophthalamides with high molecular weights containing side moieties of cyclic and acyclic ethylene oxide sequences. All the polymers were soluble in aprotic polar solvents and showed high glass‐transition temperatures in the range of 190–345 °C. The polymers with side crown ethers showed much higher glass‐transition temperatures than those with acyclic linear side ethylene oxide arms. The chemical composition, particularly with respect to the diamine and the open or closed character of the pendent ethylene oxide sequence, also affected other general properties such as the mechanical resistance, mechanical modulus, or water absorption. © 2006 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 44: 4063–4075, 2006 相似文献
119.
Simone Cristoni Laura Molin Antonella Lai Luigi Rossi Bernardi Salvatore Pucciarelli Marco Agostini Chiara Bedin Donato Nitti Roberta Seraglia Ombretta Repetto Vincenza Flora Dibari Rosaria Orlandi Pablo Martínez‐Lozano Sinues Pietro Traldi 《Rapid communications in mass spectrometry : RCM》2009,23(17):2839-2845
120.
Juan J. Ferreiro José G. de la Campa Angel E. Lozano J. de Abajo Jack Preston 《Journal of polymer science. Part A, Polymer chemistry》2008,46(22):7566-7577
Novel aromatic polyamides have been prepared by a combination of diacids containing preformed benzimidazole rings and aromatic diamines. By the phosphorylation method of polycondensation, polymers of high molecular weight (inherent viscosities between 0.81 and 2.13 dL/g) were obtained, which showed good solubility in polar aprotic solvents. The combination of aromatic amide linkages and benzimidazole rings along the polymer chain endowed the polymers with high thermal resistance and excellent mechanical properties. Glass transition temperatures fell in the range of 290–330 °C as measured by differential scanning calorimetry, and initial decomposition temperatures under nitrogen were over 480 °C as measured by thermogravimetric analysis. Some polymer films showed outstanding tensile strength (over 150 MPa) and moduli (up to 5 GPa). The presence of benzimidazole rings in the current polyamides greatly enhanced their hydrophilicity in comparison with classical wholly aromatic polyamides; thus, although aromatic polyamide films normally show water sorption values of only 4–8%, some of the current poly(benzimidazole amide)s show water sorption up to 19% in a 65% relative humidity atmosphere. © 2008 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 46: 7566–7577, 2008 相似文献