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排序方式: 共有1538条查询结果,搜索用时 46 毫秒
41.
Alexander Glozman Efrat Lifshitz Kathrin Hoppe Ahdrey L. Rogach Horst Weller Alexander Echymüller 《Israel journal of chemistry》2001,41(1):39-44
The optical properties of thiol-stabilized CdTe nanocrystals have been examined. The thiol groups -SR generate a CdS shell at the interface, leading to a CdTe/CdS core—shell structure. The present paper describes our efforts to identify the influence of the CdTe–SR interface on the optical properties of the nanocrystals, utilizing photoluminescence and optically detected magnetic resonance (ODMR) spectroscopy. The photoluminescence spectrum consists of an excitonic peak, overlapped by a broad band at lower energies. The ODMR spectrum, in the spectral regime of the broad band, showed two resonance signals. They are associated with a trapped hole at an anisotropic site of a cadmium vacancy at the Cd–SR interface and an electron in the conduction band. 相似文献
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This contribution provides insight on the elimination of heavy metals from water resources using magnetic separation. Nanocomposites based on magnetite and chitosan were prepared. An exhaustive characterization of the magnetic adsorbents was developed. Adsorption assays were performed in batch using Cu, Zn, Cd, and Cr as model heavy metals. The efficiency of magnetic adsorbents followed the order: Cu > Cd > Zn > Cr, with maximum values of 188, 159, 72, and 46 mg of Me/g of nanocomposite, respectively. Kinetics and mechanistic issues were studied. The magnetic materials were efficient for five to eight cycles using Cu(II),Cd(II), and Cr(VI). 相似文献
44.
Michael Herrmann Ulrich Frter‐Barth Manfred A. Bohn Horst Krause Michael Koch Werner Arnold 《Propellants, Explosives, Pyrotechnics》2015,40(6):880-885
Non‐destructive X‐ray diffraction techniques were applied in order to monitor the influence of mechanical and shock‐loading on the microstructure of the plastic‐bonded high explosive KS32. The investigations uncovered damage to embedded coarse HMX crystals and to the binder system HTPB‐IPDI. Damage to the crystals occurred already during the kneading process in terms of deformation twinning. On higher loading between 400 MPa (static) and 480 MPa (dynamic) also crystal fracture was observed. The change in the binder structure was found after both static and dynamic loading, but not in the cured, differently kneaded samples. Moreover, the change in binder structure after dynamic loading was verified by dynamic mechanical analysis, and interpreted as a partial damage of the binder rubber shell around the explosive particles. The results are compared to literature data from imaging techniques. 相似文献
45.
Effect of Constant‐Rate Reduction on the Performance of a Ternary Cu/ZnO/Al2O3 Catalyst in Methanol Synthesis
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A multi‐functional flow set‐up was developed for the rate‐ and temperature‐controlled reduction of copper catalysts, their application in high‐pressure methanol synthesis and the determination of the copper surface area by N2O frontal chromatography. The influence of constant‐rate reduction on the catalytic properties of a ternary Cu/ZnO/Al2O3 catalyst was investigated. The temperature during the constant‐rate reduction was found to decrease, indicating autocatalytic kinetics, but no significant catalytic effect of the milder reduction conditions was observed compared with a slow linear heating ramp. 相似文献
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Horst Hennig Klaus Ritter Roland Billing 《Advanced Synthesis \u0026amp; Catalysis》1996,338(1):604-613
Photocatalytic Hydrogen Formation from Thioles in the Presence of Vitamin-B12 Model Complexes with Azide as Photochemical Sacrificial Ligand The photolysis of [N3Co(chelat)B] complexes ( 1–3 ) (chelat = dimethylglyoxime, dmg; N,N′-o-phynylenebis(salicylidenimine), salphen; N,N′-ethylene-bis(salicylidenimine), salen; B = pyridine) leads by homolytic cleavage of the Co–N3 bond to both coordinatively unsaturated cobalt(II) chelates [Co(chelat)B] and N3 ligand radicals that undergo fast decay to dinitrogen. The photolysis of the cobalt (III) complexes 1–3 in the presence of thiophenole and other thioles proceeds catalytically and yields the corresponding disulphides and dihydrogen. The mechanism of this photocatalytic generation of dihydrogen is due to the catalytic activity of the coordinatively unsaturated cobalt(II) species formed photochemically. A photocatalytic cycle is proposed describing the generation of hydrogen. Possible photochemical and thermal steps of that cycle are discussed. 相似文献
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Photochemistry of Azido and Thiolato Vitamin-B12 Model Complexes as Precursor Compounds for Coordinatively Unsaturated Cobalt(II) Complexes The photolysis of [LCo(chelat)B] complexes ( 1–3 ) (L = azide, N; thiolate, RS−; chelat = dimethylglyoxime, dmg; N,N′-o-phenylene-bis(salicylidenimine), salphen; N,N′-ethylene-bis(salicylidenimine), salen; B = pyridine, imidazole, triphenylphosphine) leads upon the homolytic cleavage of the Co L bond to both coordinatively unsaturated reactive cobalt(II) chelates [Co(chelat)B] and ligand radicals L•. The efficiency of these photochemical redox reactions is described in relation to the structure of the cobalt(III) chelates, the wavelength of irradiation, the light-intensity as well as the solvents and substrates used during the photochemical experiments. Further, sensitization experiments using [Ru(bipy)3]Cl2 as sensitizer are described and the redox potentials of the investigated complexes are discussed. 相似文献