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Kinetics and Thermodynamic Parameters of the CopperExchange on Na-montmorillonite Clay Mineral inSelected Solvents
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作者 A.A.Zaghlou M.EI-Batouty and Sh.A.Shazly (Chemistry Dept., Faculty of Science, Alexandria University, Alexandria, Egypt) 《Journal of Materials Science & Technology》 SCIE EI CAS CSCD 1995年第4期265-268,共4页
The kinetics of Cu ion exchange on Na-montmorillonite clay mineral has been investigated at three temperatures, in three solvents: H2O, ethylene glycol and glycerol. Solvent effects on the reaction rate have been disc... The kinetics of Cu ion exchange on Na-montmorillonite clay mineral has been investigated at three temperatures, in three solvents: H2O, ethylene glycol and glycerol. Solvent effects on the reaction rate have been discussed. The thermodynamic activation parameters were calculated and discussed in terms of solvation effects. The determined isokinetic temperature indicates that the reaction is enthalpy controlled where the interaction between solvent and clay surface plays an important role. A reaction mechanism which describes the solvent effect on the rate of Cu ion exchange is proposed. 展开更多
关键词 NA Kinetics and Thermodynamic Parameters of the CopperExchange on na-montmorillonite Clay Mineral inSelected Solvents
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Preparation and Photochemical Behavior of a Cationic Azobenzene Dye-Montmorillonite Intercalation Compound 被引量:2
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作者 万涛 《Journal of Wuhan University of Technology(Materials Science)》 SCIE EI CAS 2007年第3期466-469,共4页
Montmorillonite/cationic azobenzene dye(p-(δ-triethylammoniobutoxy)-p'-methyl- azobenzene bromide) intercalation compounds were prepared by the conventional ion exchange method. As compared with that of pure cat... Montmorillonite/cationic azobenzene dye(p-(δ-triethylammoniobutoxy)-p'-methyl- azobenzene bromide) intercalation compounds were prepared by the conventional ion exchange method. As compared with that of pure cationic azo-dye, the thermal stability of the intercalated dye was greatly enhanced, and the absorption band corresponding to azobenzene group in intercalated dye shifted towards longer wave length by 38 nm. This could be ascribed to the strong conjugation of cationic azo-dye supramolecular order structure(J cluster) confined in a nanoscale space of montmorillonite interlayer gallery. UV/vis spectra data show that the intercalated azo dye in the montmorillonite interlayer space exhibited reversible trans-to-cis photoisomerization and daylight cis-to-trans back reaction. FTIR indicates the successful intercalation of cationic azo-dye into the montmorillonite interlayer. 展开更多
关键词 na-montmorillonite AZOBENZENE INTERCALATION PHOTOISOMERIZATION
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Preparation of a cationic azobenzene dye-montmorillonite intercalation compound and its photochemical behavior 被引量:1
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作者 Tao Wan Yi Yuan Wenqiong He 《Journal of University of Science and Technology Beijing》 CSCD 2006年第3期281-286,共6页
Montmorillonite/cationic azobenzene dye (GTL) intercalation compounds were prepared by the conventional ion exchange method. As compared with that of pure GTL, the thermal stability of the intercalated GTL was great... Montmorillonite/cationic azobenzene dye (GTL) intercalation compounds were prepared by the conventional ion exchange method. As compared with that of pure GTL, the thermal stability of the intercalated GTL was greatly enhanced, and the absorption band corresponding to azobenzene group in intercalated GTL shifted towards a longer wavelength by 55 nm, which could be ascribed to the strong conjugation of GTL supramolecular order structure (J cluster) confined in a nanoscale space of montmorillonite interlayer gallery. The microstructures of the resulting intercalation compounds could be successfully controlled by varying the amount of dye loaded as evidenced by the basal spacing of the intercalation compounds. The intercalated azo dye in the montmorillonite interlayer space exhibited reversible trans-to-cis photoisomerization and thermal cis-to-trans reaction. FTIR proved the successful intercalation of GTL into the silicate layer. 展开更多
关键词 na-montmorillonite AZOBENZENE INTERCALATION PHOTOISOMERIZATION
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