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1.
用电活性分子——硬脂酸二茂铁酯L-B膜修饰了薄膜CdSe电极,在单色光650nm光照下用循环伏安法研究修饰的薄膜电极的光电化学性能。研究结果指出经多层L-B膜修饰后,薄膜CdSe电极的,I-V性能和光稳定性都有明显改善。用界面能级关系讨论了硬脂酸二茂铁酯L-B膜在光照的CdSe薄膜/Fe(CN)_6~(4-)溶液界面起传递电荷的中介作用,加速了界面的电荷转移。  相似文献   
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Chemical physical analysis, photo‐oxidative stability and lipid oxidation of innovative polymeric films based on blends of nylon 6 and ethylene‐co‐vinyl alcohol for use in food packaging have been investigated. Thermal mechanical analysis showed that the presence of an interfacial agent in the blend stabilized the films towards the action of permeants. Synergistic effects of the interfacial agent are reported with respect to UV photostability. Peroxide value (PV) was used to follow the oxidation of the olive oil, and for this parameter also the influence of the interfacial agent was clearly detected. Copyright © 2001 John Wiley & Sons, Ltd.  相似文献   
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辣椒红色素的分离及光稳定性研究   总被引:8,自引:0,他引:8       下载免费PDF全文
利用硅胶柱层析法分离辣椒红色素,得到黄色素酯和辣椒红素二酯,比较它们的光稳定性。结果表明,在光照条件下,辣椒红素二酯稳定性较高,4d后仍有50%未被降解;避光存放3个月,辣椒红素二酯最稳定,降解率不到0.5%,而混合色素的稳定性降低。  相似文献   
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A series of four stable synthetic bacteriochlorins was tested in vitro in HeLa cells for their potential in photodynamic therapy (PDT). The parent bacteriochlorin (BC), dicyano derivative (NC)2BC and corresponding zinc chelate (NC)2BC–Zn and palladium chelate (NC)2BC–Pd were studied. Direct dilution of a solution of bacteriochlorin in an organic solvent (N,N‐dimethylacetamide) into serum‐containing medium was compared with the dilution of bacteriochlorin in Cremophor EL (CrEL; polyoxyethylene glycerol triricinoleate) micelles into the same medium. CrEL generally reduced aggregation (as indicated by absorption and fluorescence) and increased activity up to tenfold (depending on bacteriochlorin), although it decreased cellular uptake. The order of PDT activity against HeLa human cancer cells after 24 h incubation and illumination with 10 J cm?2 of near‐infrared (NIR) light is (NC)2BC–Pd (LD50=25 nM ) > (NC)2BC > (NC)2BC–Zn ≈ BC. Subcellular localization was determined to be in the endoplasmic reticulum, mitochondria and lysosomes, depending on the bacteriochlorin. (NC)2BC–Pd showed PDT‐mediated damage to mitochondria and lysosomes, and the greatest production of hydroxyl radicals as determined using a hydroxyphenylfluorescein probe. The incorporation of cyano substituents provides an excellent motif for the enhancement of the photoactivity and photostability of bacteriochlorins as PDT photosensitizers.  相似文献   
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Significant efforts are dedicated to developing new classes of organic semiconductor materials to achieve electrically pumped lasing. However, further advancements are necessary to understand the relationship between the structure and property for the creation of innovative laser materials with high stability, low triplet yield, ultra-low lasing threshold, and low-efficiency roll-off at ultra-bright electroluminescence. Here, a new design principle is validated for organic semiconductor laser materials, demonstrating simultaneous enhancement in the key figures of merit of low amplified spontaneous emission thresholds (Eth), efficient electroluminescence, and low triplet yields. By applying the Einstein stimulated emission rate equation and Strickler–Berg approximation, Two red-emitting laser dimers of Cibalackrot with different linkers are constructed, leading to giant enhancement (≈250%) in oscillator strengths, and stimulated emission cross-sections. When blended in poly(9,9-dioctylfluorene-alt-benzothiadiazole), the new dimers achieve an ultra-low Eth (4.5 ± 0.3 µJ cm−2) in the deep red region (λASE = 655 nm), among the lowest reported for deep-red emitters. Organic light-emitting diodes (OLEDs) utilizing the dimer blend exhibit low-efficiency roll-off under DC mode. Under pulse operation, the OLEDs achieve high current densities (90 A m−2) and ultrahigh brightness (≈710 000 cd m−2). These findings highlight the dimerization design as an excellent platform to advance organic semiconductor laser materials.  相似文献   
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Au-modified CdS nanorods (100–200 nm × 5–10 nm) are synthesized via two different techniques, namely photodeposition and doping. The prepared samples are characterized by x-ray powder diffraction, transmission electron microscopy (TEM), and UV–vis and fluorescence spectroscopy. X-ray diffraction study confirmed the hexagonal phase of bare and Au-CdS samples, whereas, 5 wt% Au3+ doping into CdS resulted in a slight distortion in the crystal structure toward higher degree side. TEM images revealed the fine distribution of Au nanodeposits of size in the range of 2.5–4.5 nm on to the CdS surface in the photodeposited sample. The optical spectrum shows a significant red-shift in absorption onset (485 nm → 515 nm) and band-edge emission (505 nm → 512 nm) of CdS nanorods with the replacement of certain Cd2+ ions with Au3+. The influence of Au photodeposition and doping in CdS nanorods was comparatively tested by photooxidation of RhB (50 ppm) dye aqueous solution under direct sunlight irradiation (35–40 mWcm?2). Our results point out that 5 wt% Au3+ doping into CdS nanorods remarkably improved its activity and stability due to homogeneous dispersion of charge throughout the crystal, quick Fermi level equilibration, and an improvement in ionic bond formation.  相似文献   
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Ofloxacin (OFX) is a fluorquinolone characterized by photochemical instability. With the goal to improve its photostability in aqueous solutions, the complexation of ofloxacin with β-cyclodextrin was investigated. The complexes showed a water solubility enhancement of approximately 2.6 times; nevertheless, the photodegradation of ofloxacin was not reduced. The complexes obtained were characterized by thermal and 1H nuclear magnetic resonance (NMR) analysis, which revealed an interaction between ofloxacin and β-cyclodextrin. The last analysis indicated that only partial inclusion of the N-methylpiperazinyl moiety occurred, which can explain the fact that photostabilization was not improved. This partial inclusion phenomenon could be explained also by computer-aided molecular modeling.  相似文献   
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