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排序方式: 共有233条查询结果,搜索用时 31 毫秒
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A. Breakstone G. Claesson H. B. Crawley G. M. Dallavalle K. Doroba D. Drijard F. Fabbri A. Firestone M. A. Faessler H. G. Fischer S. Y. Fung S. Garpman W. Geist G. Giacomelli R. Gokieli M. Gorbics C. R. Gruhn P. Hanke M. Heiden W. Herr T. J. Ketel E. E. Kluge J. W. Lamsa T. Lohse I. Lund R. Mankel W. T. Meyer G. Mornacchi T. Nakada I. Otterlund M. Panter H. Pugh A. Putzer K. Rauschnabel B. Rensch F. Rimondi M. Schmelling G. P. Siroli R. Sosnowski E. Stenlund M. Szczekowski R. Szwed O. Ullaland R. Walczak D. Wegener M. Wunsch 《Zeitschrift fur Physik C Particles and Fields》1986,30(4):507-512
The relative yields of kaons and protons compared with the yield of pions at highp T and polar angles θ away from 90° (in the range from 10° to 45°) are presented forpp, dd, and αα interactions at a centre-of-mass energy \(\sqrt {s_{NN} } = 31\) GeV per nucleon-nucleon collision. The measured particle ratios depend on the atomic mass numberA of the beam particles and on θ. TheA dependence of the ratios becomes stronger for largerp T and is more pronounced at smaller polar angles. 相似文献
3.
For aqueous solutions of sodium oleate, the dynamic surface tension (using the maximum bubble pressure technique) and the equilibrium surface tensions (using the du Noüy ring method) were studied. Experiments were carried out within the pH range 7 to 13 and at temperatures from 20 to 60 degrees C. From the equilibrium surface tension studies at 25 degrees C, a wide variation in surface activity was found to occur in the premicellar concentration range, depending on pH and oleate concentration, and this was explained on the basis of the formation of strongly surface-active premicellar species. It was also shown that the critical micelle concentration (cmc) of the system increased with pH within the pH range 7-12. Dynamic surface tension experiments were carried out from 20 to 60 degrees C at concentrations beyond the cmc in alkaline solutions, and the adsorption kinetics at the air/solution interface were analyzed using established theoretical diffusion models. From these data, the effective diffusion coefficients (D(eff)) for the oleate species were determined and the presence of an interfacial activation barrier in the diffusion process was confirmed. It was found that the D(eff) values obtained within the temperature range from 40 to 60 degrees C at 2-3 mM were in general agreement with previously reported values for the oleate dimer obtained by pulse-gradient FT-NMR. Furthermore, D(eff) significantly increased with temperature and also increased with concentration at higher temperatures (>40 degrees C). Copyright 2001 Academic Press. 相似文献
4.
Hall WL Jeanes YM Pugh J Lodge JK 《Rapid communications in mass spectrometry : RCM》2003,17(24):2797-2803
A method is described for the analysis of deuterated and undeuterated alpha-tocopherol in blood components using liquid chromatography coupled to an orthogonal acceleration time-of-flight (TOF) mass spectrometer. Optimal ionisation conditions for undeuterated (d0) and tri- and hexadeuterated (d3 or d6) alpha-tocopherol standards were found with negative ion mode electrospray ionisation. Each species produced an isotopically resolved single ion of exact mass. Calibration curves of pure standards were linear in the range tested (0-1.5 microM, 0-15 pmol injected). For quantification of d0 and d6 in blood components following a standard solvent extraction, a stable-isotope-labelled internal standard (d3-alpha-tocopherol) was employed. To counter matrix ion suppression effects, standard response curves were generated following identical solvent extraction procedures to those of the samples. Within-day and between-day precision were determined for quantification of d0- and d6-labelled alpha-tocopherol in each blood component and both averaged 3-10%. Accuracy was assessed by comparison with a standard high-performance liquid chromatography (HPLC) method, achieving good correlation (r(2) = 0.94), and by spiking with known concentrations of alpha-tocopherol (98% accuracy). Limits of detection and quantification were determined to be 5 and 50 fmol injected, respectively. The assay was used to measure the appearance and disappearance of deuterium-labelled alpha-tocopherol in human blood components following deuterium-labelled (d6) RRR-alpha-tocopheryl acetate ingestion. The new LC/TOFMS method was found to be sensitive, required small sample volumes, was reproducible and robust, and was capable of high throughput when large numbers of samples were generated. 相似文献
5.
Coleen Pugh Virgil Percec 《Journal of polymer science. Part A, Polymer chemistry》1990,28(5):1101-1126
Several 1,2-(4,4'-dialkoxyaryl)acetylene monomers containing similar or dissimilar substituents were prepared by one of three variations of a one pot phase transfer Pd(O)/Cu(I) catalyzed coupling of aryl halides with a protected acetylene. The three steps within a single flask involved first coupling of the appropriate 1-halo-4-alkoxybenzene derivative with 2-methyl-3-butyn-2-ol, followed by cleavage of the carbinol group to form an aryl acetylide, and finally a second coupling of an aryl halide with the aryl acetylide. Best results were obtained when elevated temperatures and solid-liquid phase transfer reaction conditions were used. Some 1,4-bis[2-(4',4”-dialkoxyphenyl)ethynyl]benzene compounds were also prepared. 相似文献
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To study the influence of the chemical nature of headgroups and the type of counterion on the process of micellization in mixed surfactant systems, the cmc's of several binary mixtures of surfactants with the same length of hydrocarbon tail but with different headgroups have been determined as a function of the monomer composition using surface tension measurements. Based on these results, the interaction parameter between the surfactant species in mixed micelles has been determined using the pseudophase separation model. Experiments were carried out with (a) the nonionic/anionic C(12)E(6)/SDS ((hexa(ethyleneglycol) mono-n-dodecyl ether)/(sodium dodecyl sulfate)), (b) amphoteric/anionic DDAO/SDS ((dodecyldimethylamine oxide)/(sodium dodecyl sulfate)), and (c) amphoteric/nonionic C(12)E(6)/DDAO mixed surfactant systems. In the case of the mixed surfactant systems containing DDAO, experiments were carried out at pH 2 and pH 8 where the surfactant was in the cationic and nonionic form, respectively. It was shown that the mixtures of the nonionic surfactants with different kinds of headgroups exhibit almost ideal behavior, whereas for the nonionic/ionic surfactant mixtures, significant deviations from ideal behavior (attractive interactions) have been found, suggesting binding between the head groups. Molecular orbital calculations confirmed the existence of the strong specific interaction between (1) SDS and nonionic and cationic forms of DDAO and between (2) C(12)E(6) and the cationic form of DDAO. In the case for the C(12)E(6)/SDS system, an alternative mechanism for the stabilization of mixed micelles was suggested, which involved the lowering in the free energy of the hydration layer. Copyright 2000 Academic Press. 相似文献
8.
S. Budak C. SmithM. Pugh K. HeidaryT. Colon R.B. JohnsonC. Muntele D. ila 《Radiation Physics and Chemistry》2012,81(4):410-413
The performance of the thermoelectric materials and devices is shown by a dimensionless figure of merit, ZT=S2σT/K, where S is the Seebeck coefficient, σ is the electrical conductivity, T is the absolute temperature and K is the thermal conductivity. ZT can be increased by increasing S, increasing σ, or decreasing K. We have prepared the thermoelectric generator device of SiO2/SiO2+Ge multilayer superlattice films using the ion beam assisted deposition (IBAD). The 5 MeV Si ion bombardments have been performed using the AAMU Pelletron ion beam accelerator at five different fluences to make quantum structures (nanodots and/or nanoclusters) in the multilayer superlattice thin films to decrease the cross plane thermal conductivity, increase the cross plane Seebeck coefficient and cross plane electrical conductivity. To characterize the thermoelectric generator devices before and after MeV Si ions bombardments at the different fluences we have measured the cross-plane Seebeck coefficient, the cross-plane electrical conductivity, and the cross-plane thermal conductivity, Raman spectra to get some information about the sample structure and bond structures among the used elements in the superlattice thin film systems. 相似文献
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An experimental study of the thermal decomposition of a β‐hydroxy alkene, 3‐methyl‐3‐buten‐1‐ol, in m‐xylene solution, has been carried out at five different temperatures in the range of 513.15–563.15 K. The temperature dependence of the rate constants for the decomposition of this compound in the corresponding Arrhenius equation is given by ln k (s?1) = (25.65 ± 1.52) ? (17,944 ± 814) (kJ·mol?1)·T?1. A computational study has been carried out at the M05–2X/6–31+G(d,p) level of theory to calculate the rate constants and the activation parameters by the classical transition state theory. There is a good agreement between the experimental and calculated rate constants and activation Gibbs energies. The bonding characteristics of reactant, transition state, and products have been investigated by the natural bond orbital analysis, which provides the natural atomic charges and the Wiberg bond indices. Based on the results obtained, the mechanism proposed is a one‐step process proceeding through a six‐membered cyclic transition state, being a concerted and slightly asynchronous process. The results have been compared with those obtained previously by us (Struct Chem 2013, 24, 1811–1816) for the thermal decomposition of 3‐buten‐1‐ol, in m‐xylene solution. We can conclude that in the compound studied in this work, 3‐methyl‐3‐buten‐1‐ol, the effect of substitution at position 3 by a weakly activating CH3 group is the stabilization of the transition state formed in the reaction and therefore a small increase in the rate of thermal decomposition. 相似文献