全文获取类型
收费全文 | 132篇 |
免费 | 3篇 |
专业分类
化学 | 78篇 |
晶体学 | 1篇 |
力学 | 6篇 |
数学 | 8篇 |
物理学 | 42篇 |
出版年
2020年 | 3篇 |
2019年 | 3篇 |
2015年 | 1篇 |
2014年 | 2篇 |
2013年 | 2篇 |
2012年 | 3篇 |
2011年 | 8篇 |
2010年 | 5篇 |
2009年 | 3篇 |
2008年 | 14篇 |
2007年 | 7篇 |
2006年 | 4篇 |
2005年 | 5篇 |
2004年 | 1篇 |
2003年 | 2篇 |
2002年 | 1篇 |
2001年 | 3篇 |
2000年 | 3篇 |
1999年 | 2篇 |
1998年 | 2篇 |
1996年 | 1篇 |
1994年 | 4篇 |
1993年 | 4篇 |
1992年 | 6篇 |
1991年 | 2篇 |
1989年 | 4篇 |
1988年 | 1篇 |
1987年 | 1篇 |
1986年 | 1篇 |
1985年 | 2篇 |
1984年 | 1篇 |
1983年 | 1篇 |
1982年 | 4篇 |
1981年 | 4篇 |
1980年 | 2篇 |
1978年 | 1篇 |
1977年 | 2篇 |
1976年 | 2篇 |
1975年 | 3篇 |
1974年 | 1篇 |
1973年 | 6篇 |
1972年 | 2篇 |
1971年 | 2篇 |
1966年 | 1篇 |
1957年 | 1篇 |
1929年 | 1篇 |
1899年 | 1篇 |
排序方式: 共有135条查询结果,搜索用时 15 毫秒
1.
2.
A dense-phase latex rubber tube and a polyporous propylene hollow-fiber membrane module (HFMM) were investigated for control
of benzene-contaminated gas streams. The abiotic mass flux observed through the latex tube was 3.9–13 mg/(min·m2) for 150 ppm of benzene at various gas and liquid flow rates, while a 100-fold lower mass flux was observed in the HFMM.
After seeding with an aromatic-degrading culture enriched from activated sludge, the observed removal was 80% of 150 ppm,
corresponding toa mass flux of 45 mg/(min·m2). The observed mass flux through the HFMM during biofiltration also rose, to 0.4 mg/(min·m2). Because the HFMM had a 50-fold higher surface area than the latex tube, the observed ben zene removal was 99.8%. Compared
to conventional biofilters, the two reactors had modest elimination capacities, 2.5–18 g/(m3·h) in the latex tube membrane bioreactor and 4.8–58 g/(m3·h) in the HFMM. Although the HFMM had a higher elimination capacity, the gas-phase pressure drop was much greater. 相似文献
3.
4.
5.
Wong KL Bitter M Hammett GW Heidbrink W Hendel H Kaita R Scott S Strachan JD Tait G Bell MG Budny R Bush C Chan A Coonrod J Efthimion PC England AC Eubank HP Fredrickson E Furth HP Goldston RJ Grek B Grisham L Hawryluk RJ Hill KW Johnson D Kamperschroer J Kugel H Ma C Mansfield D Manos D McCune DC McGuire K Medley SS Mueller D Nieschmidt E Owens DK Paré VK Park H Ramsey A Rasmussen D Roquemore AL Schivell J Sesnic S Taylor G Williams MD Zarnstorff MC 《Physical review letters》1985,55(23):2587-2590
6.
Some reactions of amines with a perfluorovinylsulfide, (CF3)2CFSC(CF3)CFCF(CF3)2, prepared from hexafluoropropene (HFP) and sulfur [1] are compared to reactions of the same amines with the thermodynamic dimer of HFP, (CF3)2CCFCF2CF3. Many new ketenimines, eneamines, amidines, nitriles, and quinoline derivatives are reported. 相似文献
7.
N-arylsulfonyl quinone monoimines undergo smooth cycloadditions in a [4+2] sense to yield the expected cycloadducts. The crude cycloadducts, when subjected to a short series of simple transformations, produce synthetically useful quantities of 5-triflyloxyindoles in excellent overall yields. Such compounds are excellent participants in cross-coupling chemistry. 相似文献
8.
Thomas E. Sorensen Walter B. England David M. Silver E. Otto Steinborn 《Theoretical chemistry accounts》1992,84(1-2):1-19
Summary Many-body perturbation theory is derived for chemical bonds. Paired quasiparticles represent the bonds. Products of the paired quasiparticles define a model Bardeen-Cooper-Schrieffer function. The pairing force is added as a model interaction to the self-consistent problem. The starting model is based on valency and adiabatic symmetry correlation. Symmetries are enforced by the model Hamiltonian. Perturbative corrections are expressed as ordinary Feynman diagrams. The number of diagrams needed is the same as for particle-hole theory.This work was supported in part by the U.S. Department of the Navy, Space and Naval Warfare Systems Command under Contract N00039-89-C-0001, and in part by NATO Research Grant 1861. It was presented, in part, at the A.C. Wahl Memorial Session, Molecular Spectroscopy Symposium, Columbus, Ohio, 1984; and Midwest Theoretical Chemistry Conference, Milwaukee, Wisconsin, 1985. 相似文献
9.
A series of iron(II) bis(triflate) complexes containing tripodal tetradentate nitrogen ligands with pyridine and dimethylamine donors of the type [N(CH(2)Pyr)(3-n)()(CH(2)CH(2)NMe(2))(n)] [n = 0 (tpa, 1), n = 1 (iso-bpmen, 3), n = 2 (Me(4)-benpa, 4), n = 3 (Me(6)-tren, 5)] and the linear tetradentate ligand [(CH(2)Pyr)MeN(CH(2)CH(2))NMe(CH(2)Pyr), (bpmen, 2)] has been prepared. The preferred coordination geometry of these complexes in the solid state and in CH(2)Cl(2) solution changes from six- to five-coordinate in the order from 1 to 5. In acetonitrile, the triflate ligands of all complexes are readily displaced by acetonitrile ligands. The complex [Fe(1)(CH(3)CN)(2)](2+) is essentially low spin at room temperature, whereas ligands with fewer pyridine donors increase the preference for high-spin Fe(II). Both the number of pyridine donors and the spin state of the metal center strongly affect the intensity of a characteristic MLCT band around 400 nm. The catalytic properties of the complexes for the oxidation of alkanes have been evaluated, using cyclohexane as the substrate. Complexes containing ligands 1-3 are more active and selective catalysts, possibly operating via a metal-based oxidation mechanism, whereas complexes containing ligands 4 and 5 give rise to Fenton-type chemistry. 相似文献
10.
Britovsek GJ England J Spitzmesser SK White AJ Williams DJ 《Dalton transactions (Cambridge, England : 2003)》2005,(5):945-955
A series of Fe(II), Mn(II), Co(II) and Ru(II) complexes containing bis(imino)pyridine or bis(amino)pyridine ligands and weakly coordinating triflate (OTf-) or non-coordinating SbF6- anions have been prepared. The complexes have been fully characterized including several solid-state structure analyses. Two unusual mono-chelate six-coordinate bis(imino)pyridine Fe(II) and Mn(II) complexes have been observed. The catalytic properties of the complexes for the oxidation of cyclohexane with H2O2 have been evaluated. Only the Fe(II) complexes have shown catalytic activity, which is mainly due to Fenton-type free radical auto-oxidation. 相似文献