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51.
The voltammetric response of nitrogen dioxide in aqueous sulfuric acid using an edge plane pyrolytic graphite electrode has been explored and contrasted with that from basal plane pyrolytic graphite, glassy carbon or boron-doped diamond electrodes. Edge plane graphite electrode is found to produce an excellent voltammetric signal in comparison with other carbon-based electrodes exhibiting a well-defined analytically useful voltammetric redox couple in 2.5 M sulfuric acid which is absent on the alternative electrodes. 相似文献
52.
R. J. Gehrke E. W. Killian L. V. East J. M. Hoggan S. G. Goodwin G. D. McLaughlin 《Journal of Radioanalytical and Nuclear Chemistry》1998,233(1-2):225-231
A portable, battery-powered, multichannel analyzer (MCA) for use with Ge spectrometers has been developed for in-field use
for the assay of x-and γ-ray emitting radionuclides. The spectrometer is capable of operating to rates greater than 150,000
counts per second. The analyzer is a Canberra InSpector MCA, that is equipped with the INEEL ultra-stable dual-energy pulser,
and pulse injection with subsequent removal (PISR) circuitry. PCGAP, a set of MCA control and spectral analysis programs,
was developed for use on a PC with a Windows NT Operating System. It includes an interactive peak analysis program as well
as automatic spectral analysis programs for the X- and γ-ray regions, and a number of utility programs. The pulser peaks are
calibrated with radioactive sources in terms of energy (i.e., their energy equivalents are measured) using the PCGAP spectral
analysis package so that energy shifts, including those due to changes in temperature or count rate, do not cause a loss of
energy calibration. The number of injected low- and high-energy-equivalent pulses is known so the stored pulser pulses can
be used for a dead-time and random summing correction. The pulser peaks are also used to monitor any deterioration in spectral
quality caused by noise, ground loops, etc. The results of performance tests to demonstrate the capabilities of this pulser-equipped
InSpector are reported. 相似文献
53.
Summary It is shown that the retention indices of polar solutes are affected by the amount of stationary phase in the column. The retention indices increase with decreasing stationary phase loadings. The reasons for this behavior are most likely due to the existence of mixed retention mechanisms. At low amounts of stationary phases, adsorption on the support or column walls can take place. Studies were made using four supports, two of which were Chromosorb W and the other two Chromosorb P. The effects of changing the liquid phase loadings are more pronounced when using Chromosorb P. 相似文献
54.
55.
56.
Abstract A facile procedure is presented for the synthesis of (E)-1-(3′-hydroxy-2′-furanyl)-3-(3″-hydroxy-4″-methoxyphenyl)-2- propen-1-one (6). Galactosylisomaltol (1) was condensed with isovanillin (2) under strong alkaline conditions at 25 [ddot]C to form (E)-1-(3′-O-β-D-galactopyranosyloxy-2′-furanyl)-3-(3″- hydroxy-4″-methoxyphenyl)-2-propen-1-one (4). (E)-1-(3′-hydroxy-2′-furanyl)-3-(3″-hydroxy-4″-methoxyphenyl)-2-propen-1-one (6) was obtained by acid hydrolysis of 4 in a 53.9% yield. This hetero-cyclic 2-propen-1-one was characterized on the basis of spectral data (IR and 1H NMR), physicochemical properties, and conversion to a mono-O-acetyl derivative. 相似文献
57.
Márcio AF Belo-Filho Franklina MB Toledo Bernardo Almada-Lobo 《The Journal of the Operational Research Society》2014,65(11):1735-1747
Setup operations are significant in some production environments. It is mandatory that their production plans consider some features, as setup state conservation across periods through setup carryover and crossover. The modelling of setup crossover allows more flexible decisions and is essential for problems with long setup times. This paper proposes two models for the capacitated lot-sizing problem with backlogging and setup carryover and crossover. The first is in line with other models from the literature, whereas the second considers a disaggregated setup variable, which tracks the starting and completion times of the setup operation. This innovative approach permits a more compact formulation. Computational results show that the proposed models have outperformed other state-of-the-art formulation. 相似文献
58.
Harvey SD Mong GM Ozanich RM McLean JS Goodwin SM Valentine NB Fredrickson JK 《Analytical and bioanalytical chemistry》2006,386(2):211-219
A novel, affinity-augmented, bacterial spore-imprinted, bead material was synthesized, based on a procedure developed for
vegetative bacteria. The imprinted beads were intended as a front-end spore capture/concentration stage of an integrated biological
detection system. Our approach involved embedding bead surfaces with Bacillus thuringiensis kurstaki (Bt) spores (as a surrogate for Bacillus anthracis) during synthesis. Subsequent steps involved lithographic deactivation using a perfluoroether; spore removal to create imprint
sites; and coating imprints with the lectin, concanavalin A, to provide general affinity. The synthesis of the intended material
with the desired imprints was verified by scanning electron and confocal laser-scanning microscopy. The material was evaluated
using spore-binding assays with either Bt or Bacillus subtilis (Bs) spores. The binding assays indicated strong spore-binding capability and a robust imprinting effect that accounted for 25%
additional binding over non-imprinted controls. The binding assay results also indicated that further refinement of the surface
deactivation procedure would enhance the performance of the imprinted substrate. 相似文献
59.
60.
Kieran W. P. Orr Sean M. Collins Emily M. Reynolds Frank Nightingale Hanna L. B. Bostrm Simon J. Cassidy Daniel M. Dawson Sharon E. Ashbrook Oxana V. Magdysyuk Paul A. Midgley Andrew L. Goodwin Hamish H.-M. Yeung 《Chemical science》2021,12(12):4494
Control over the spatial distribution of components in metal–organic frameworks has potential to unlock improved performance and new behaviour in separations, sensing and catalysis. We report an unprecedented single-step synthesis of multi-component metal–organic framework (MOF) nanoparticles based on the canonical ZIF-8 (Zn) system and its Cd analogue, which form with a core–shell structure whose internal interface can be systematically tuned. We use scanning transmission electron microscopy, X-ray energy dispersive spectroscopy and a new composition gradient model to fit high-resolution X-ray diffraction data to show how core–shell composition and interface characteristics are intricately controlled by synthesis temperature and reaction composition. Particle formation is investigated by in situ X-ray diffraction, which reveals that the spatial distribution of components evolves with time and is determined by the interplay of phase stability, crystallisation kinetics and diffusion. This work opens up new possibilities for the control and characterisation of functionality, component distribution and interfaces in MOF-based materials.Core–shell metal–organic framework nanoparticles have been synthesised in which the internal interface and distribution of components is found to be highly tunable using simple variations in reaction conditions. 相似文献