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排序方式: 共有137条查询结果,搜索用时 15 毫秒
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R. Spatz und K. H. Lieser 《Fresenius' Journal of Analytical Chemistry》1977,288(4):267-272
Zusammenfassung Bei Verwendung einer Röntgenröhre mit Sekundärtargets kann durch geeignete Wahl des Sekundärtargets eine hohe Nachweisempfindlichkeit im Bereich bestimmter Ordnungszahlen erreicht werden. Für schwere Elemente ist die Messung der L-Linien vorteilhaft. Bei Verwendung von Radionuklidquellen werden etwa die gleichen Nachweisgrenzen erreicht. Im Bereich hoher Energien sind Radionuklidquellen besonders günstig.
Critical comparison of the measuring range and detection limits in energy-dispersive X-ray fluorescence analysis with tube excitation (secondary target) and with radionuclide excitation (Cd-109 and Am-241), by means of bulk powder samples on silicagel basis as an example
Summary Using a X-ray tube in combination with secondary targets by proper choice of the secondary target high detection limits for ranges of certain atomic numbers are obtained. In the case of heavy elements measurement of L-lines is more favourable. By use of radionuclides as X-ray sources nearly the same detection limits are obtained. In the range of high energies the application of radionuclides has distinct advantages.
Wir danken dem BMFT für finanzielle Unterstützung. 相似文献
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The analysis of dust samples by X-ray fluorescence using Cd-109 as X-ray source is described. For calibration silica gel standards are used. The correction for matrix effects is carried out by means of the Compton peaks. Besides the elements K, Ca, Ti, Fe, Rb, Sr, Y, Zr, which may be considered to be natural components of the ground, the elements Cr, Mn, Ni, Cu, Zn, Br and Pb are determined in the dust samples. 相似文献
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Le Faou JH Suomijärvi T Blumenfeld Y Piattelli P Agodi C Alamanos N Alba R Auger F Bellia G Chomaz P Coniglione R Del Zoppo A Finocchiaro P Frascaria N Gaardhoje JJ Garron JP Gillibert A Lamehi-Rachti M Liguori-Neto R Maiolino C Migneco E Russo G Roynette JC Santonocito D Sapienza P Scarpaci JA Smerzi A 《Physical review letters》1994,72(21):3321-3324
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Akiba Y Beavis D Beery P Britt HC Budick B Chasman C Chen Z Chi CY Chu YY Cianciolo V Cole BA Costales JB Crawford HJ Cumming JB Debbe R Engelage J Fung SY Gonin M Gushue S Hamagaki H Hansen O Hayano RS Hayashi S Homma S Kaneko H Kang J Kaufman S Kehoe WL Kurita K Ledoux RJ Levine MJ Miake Y Morrison DP Morse RJ Moskowitz B Nagamiya S Namboodiri MN Nayak TK Olness J Parsons CG Remsberg LP Roehrich D Rothschild P Sakurai H Sangster TC Seto R Soltz R Stankus P Steadman SG Stephans GS Sung T 《Physical review letters》1996,76(12):2021-2024
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Lenhart JL van Zanten JH Dunkers JP Zimba CG James CA Pollack SK Parnas RS 《Journal of colloid and interface science》2000,221(1):75-86
Silane coupling agents are commonly applied to glass fibers to promote fiber/resin adhesion and enhance durability in composite parts. In this study, a coupling agent multilayer on glass was doped with trace levels of the dimethylaminonitrostilbene (DMANS) fluorophore. The fluorophore was immobilized on the glass surface by tethering the molecule to a triethoxy silane coupling agent, creating the DMANS/silane coupling agent molecule (DMSCA). DMSCA was then diluted with commonly used coupling agents and grafted to a glass microscope coverslip to create a model composite interface. A 53-nm blue shift in fluorescence from the immobilized DMSCA can be followed during cure of an epoxy resin overlayer, giving this technique potential to monitor the properties of the fiber/resin interface during composite processing. Contact angle measurements on these coupling agent layers were similar in the presence or absence of the DMSCA molecule, suggesting that trace levels of the fluorescent probe did not affect the structure of the layer. The immobilized DMSCA molecule behaved similarly to the DMANS precursor in solution. Both showed longer wavelength fluorescence in more polar environments. Copyright 2000 Academic Press. 相似文献
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Garcia Ruano JL Alemparte C Martin Castro AM Adams H Rodriguez Ramos JH 《The Journal of organic chemistry》2000,65(23):7938-7943
The behavior of (Z)-3-p-tolylsulfinylacrylonitrile (1) as a chiral dienophile has been evaluated from its reactions with furan and acyclic dienes. Electrostatic interactions of the cyano group with the sulfinyl one restrict the conformational mobility around the C-S bond, thus controlling the pi-facial selectivity, which is almost complete in all cases, the approach of the diene from the less-hindered face of the dienophile (that bearing the lone electron pair) in the predominant rotamer being the favored one. The regioselectivity is also completely controlled by the cyano group. Additionally, the reactivity of compound 1 as well as its endo-selectivity are both higher than those observed for the corresponding (Z)-3-sulfinylacrylates, thus proving the potential of sulfinylnitriles as chiral dienophiles. 相似文献
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