全文获取类型
收费全文 | 96篇 |
免费 | 0篇 |
国内免费 | 2篇 |
专业分类
化学 | 52篇 |
数学 | 13篇 |
物理学 | 33篇 |
出版年
2023年 | 1篇 |
2021年 | 1篇 |
2018年 | 4篇 |
2017年 | 4篇 |
2016年 | 4篇 |
2014年 | 2篇 |
2013年 | 1篇 |
2012年 | 2篇 |
2011年 | 3篇 |
2010年 | 2篇 |
2009年 | 2篇 |
2008年 | 3篇 |
2007年 | 3篇 |
2006年 | 4篇 |
2005年 | 5篇 |
2004年 | 5篇 |
2003年 | 4篇 |
2002年 | 7篇 |
2001年 | 4篇 |
2000年 | 2篇 |
1999年 | 2篇 |
1996年 | 1篇 |
1993年 | 2篇 |
1991年 | 1篇 |
1990年 | 2篇 |
1987年 | 1篇 |
1986年 | 2篇 |
1985年 | 1篇 |
1983年 | 1篇 |
1981年 | 2篇 |
1980年 | 3篇 |
1978年 | 1篇 |
1977年 | 2篇 |
1976年 | 3篇 |
1975年 | 2篇 |
1969年 | 1篇 |
1967年 | 2篇 |
1964年 | 1篇 |
1955年 | 1篇 |
1948年 | 1篇 |
1937年 | 1篇 |
1923年 | 2篇 |
排序方式: 共有98条查询结果,搜索用时 31 毫秒
1.
The free solution mobility of a high-molecular-weight DNA, linear pUC19, and a 20-bp oligomer called dsA5 have been studied as a function of Tris-acetate-EDTA (TAE) buffer concentration, with and without added NaCl. The two DNAs migrate as separate peaks during capillary electrophoresis, because the mobility of linear pUC19 is higher than that of the 20-bp oligomer. In TAE buffers ranging from 10-400 mM in concentration, the migration times and peak areas of the two DNAs are independent of whether they are electrophoresed separately or in mixtures, indicating that DNA-DNA and DNA-buffer interactions are absent in these solutions. The migration times of the two DNAs vary and the peak areas are not additive when the TAE buffer concentration is reduced to 5 mM or below, indicating that DNA-DNA and DNA-buffer interactions are occurring at very low TAE buffer concentrations. The mobilities of linear pUC19 and dsA5 decrease slowly with increasing conductivity or ionic strength when the conductivity is increased by increasing the TAE buffer concentration. When the Tris buffer concentration is held constant and the conductivity is increased by adding various concentrations of NaCl to the solution, the mobilities of linear pUC19 and dsA5 first increase slightly, then become independent of solution conductivity (or ionic strength), and finally decrease when the NaCl concentration is increased above approximately 50 mM. The mobility variations observed in the various TAE and TAE-NaCl solutions are described qualitatively by Manning's theory, although quantitative agreement is not achieved. The free solution mobilities of single-stranded pUC19 and two 20-base oligonucleotides have also been measured. The free solution mobility of single-stranded pUC19 is approximately 15% lower than that of native pUC19, in agreement with other results in the literature. Somewhat surprisingly, the mobilities of the single- and double-stranded 20-mers are equal to each other in TAE buffers with and without added NaCl. 相似文献
2.
Chynoweth D. P. Bosch G. Earle J. F. K. Legrand Robert Liu Kexin 《Applied biochemistry and biotechnology》1991,(1):421-432
A novel process has been developed and evaluated in a pilotscale program for conversion of the biodegradable fraction of municipal
solid waste (MSW) to methane via anaerobic composting. The sequential batch anaerobic composting (SEBAC) process employs leachate
management to provide organisms, moisture, and nutrients required for rapid conversion of MSW and removal of inhibitory fermentation
products during start-up. The biodegradable organic materials are converted to methane and carbon dioxide in 21–42 d, rather
than the years required in landfills. 相似文献
3.
The enthalpies of transfer of 2-methyl-2-propanol (TBA) from water to mixtures of water with methanol, ethanol and 1,4-dioxane
have been measured. The data are considered in terms of recently developed theory, and it is found that the enthalpies of
transfer can be reproduced quantitatively over most of the composition range in each solvent system. The parameters recovered
from the analyses indicate that the net effect of TBA on the solvent structure is a breaking of solvent-solvent bonds and
that TBA is preferentially hydrated in the aqueous alcohol systems, but randomly solvated in the water+1,4-dioxane system.
It is also found that the model parameters for TBA solvation in the alcohol systems are independent of the alcohol. 相似文献
4.
5.
Ahmed SN Anthony AE Beier EW Bellerive A Biller SD Boger J Boulay MG Bowler MG Bowles TJ Brice SJ Bullard TV Chan YD Chen M Chen X Cleveland BT Cox GA Dai X Dalnoki-Veress F Doe PJ Dosanjh RS Doucas G Dragowsky MR Duba CA Duncan FA Dunford M Dunmore JA Earle ED Elliott SR Evans HC Ewan GT Farine J Fergani H Fleurot F Formaggio JA Fowler MM Frame K Fulsom BG Gagnon N Graham K Grant DR Hahn RL Hall JC Hallin AL Hallman ED Hamer AS Handler WB Hargrove CK Harvey PJ Hazama R Heeger KM Heintzelman WJ 《Physical review letters》2004,92(18):181301
The Sudbury Neutrino Observatory has precisely determined the total active (nu(x)) 8B solar neutrino flux without assumptions about the energy dependence of the nu(e) survival probability. The measurements were made with dissolved NaCl in heavy water to enhance the sensitivity and signature for neutral-current interactions. The flux is found to be 5.21 +/- 0.27(stat)+/-0.38(syst) x 10(6) cm(-2) s(-1), in agreement with previous measurements and standard solar models. A global analysis of these and other solar and reactor neutrino results yields Deltam(2)=7.1(+1.2)(-0.6) x 10(-5) eV(2) and theta=32.5(+2.4)(-2.3) degrees. Maximal mixing is rejected at the equivalent of 5.4 standard deviations. 相似文献
6.
Misra SK Andronenko SI Rinaldi G Chand P Earle KA Freed JH 《Journal of magnetic resonance (San Diego, Calif. : 1997)》2003,160(2):131-138
Multifrequency electron paramagnetic resonance studies on the Mn(2+) impurity ion in a mixed single crystal NH(4)Cl(0.9)I(0.1) were carried out at 9.62 (X-band) in the range 120-295 K, at 35.87 (Q-band) at 77 and 295 K, and at 249.9 GHz (far-infrared band) at 253 K. The high-field EPR spectra at 249.9 GHz are well into the high-field limit leading to a considerable simplification of the spectra and their interpretation. Three magnetically inequivalent, but physically equivalent, Mn(2+) ions with their respective magnetic Z-axes oriented along the crystallographic [100], [010], [001] axes were observed. Simultaneous fitting of EPR line positions observed at X-, Q-, and far infra-red bands was performed using a least-squares procedure and matrix diagonalization to estimate accurately the Mn(2+) spin-Hamiltonian parameters. The temperature variation of the linewidth and peak-to-peak intensities of the EPR lines indicate the presence of lambda-transitions in the mixed NH(4)Cl(0.9)I(0.1) crystal at 242 and 228 K consistent with those observed in the pure NH(4)Cl and NH(4)I crystals, respectively. A superposition-model analysis of the spin-Hamiltonian parameters reveals that the local environment of the Mn(2+) ion is considerably reorganized to produce axially symmetric crystal fields about the respective Z-axes of the three magnetically inequivalent ions as a consequence of the vacancy created due to charge-compensation when the divalent Mn(2+) ion substitutes for a monovalent NH(4)(+) ion in the NH(4)Cl(0.9)I(0.1) crystal. This reorganization is almost the same as that observed in NH(4)Cl and NH(4)I single crystals, although the latter two are characterized by different, simple cubic and face-centered cubic, structures. 相似文献
7.
8.
Capillary zone electrophoresis is employed for the separation and analysis of both fluorescein thiohydantoin and dimethylaminoazobenzene thiohydantoin derivatives of amino acids. Detection of minute amounts of these amino acid derivatives is an important milestone in the development of a high sensitivity protein sequencer. Current detection limits for the fluorescein derivative is on the order of 10(-21) moles whereas detection limits for the dimethylaminoazobenzene derivative is on the order of 10(-16) moles. 相似文献
9.
W. Earle Waghorne 《Journal of solution chemistry》2017,46(9-10):1818-1835
A theorem presented by Professor Ben-Naim (J Phys Chem 82:874–885, 1978) states that the standard state enthalpy and entropy changes arising from changes in the solvent structure that are induced by solvation of a solute cancel exactly in the standard state Gibbs energy. In this paper this is explored by consideration of the thermodynamics of transfer of electrolytes in mixed solvents, using previously developed models of the solvation process. Two cases are considered. One is random solvation, where curvatures in plots of the transfer enthalpies and entropies, which arise from changes in solvent–solvent interactions, exactly compensate in the transfer Gibbs (free) energies, which are sensibly linear with solvent composition. The second type of system are those with strong preferential solvation where it is found that the transfer Gibbs energies can be accounted for quantitatively in terms of changes in the solute–solvent interactions, with no contribution from changes in solvent–solvent interactions. The results are entirely consistent with the Ben-Naim theorem. 相似文献
10.
John Earle Black 《Surface science》1980,100(3):555-560
One atom phonon spectral densities are presented for the vibrations of atoms at the Ni(111) surface both parallel and perpendicular to the surface. They are also presented for perpendicular motion of an adsorbed oxygen atom and the nickel atom immediately below it. The results are obtained using a continued fraction technique. They are compared with recent EELS data obtained by Ibach and Bruchmann. 相似文献