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The effects of water vapor and temperature on the phase transition between anhydrous N,N-ethylenebis(acetylacetoniminato) copper (II) and the monohydrate have been studied by a piezoelectric microbalance method. The presence of a branch point and critical deceleration of the phase transition dynamics near that point have been observed.Translated from Teoreticheskaya i Éksperimental'naya Khimiya, Vol. 29, No. 2, pp. 149–153, March–April, 1993.This work was supported by a fundamental research grant from the State Committee on Science and Technology, Ukraine Council of Ministers. 相似文献
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O. V. Kuraev V. N. Grebennikov S. N. Zavodovskii S. B. Grinenko L. I. Budarin 《Theoretical and Experimental Chemistry》1993,28(3):184-187
Using optical microscopy and thermogravimetry, we have established that determination of the kinetic characteristics of dissociation for the monoaquo adduct of copper N,N-ethylene-bis(acetylacetoniminate) with particle size 0.5–2 mm is hindered by self-dispersal processes. Using a piezoquartz microbalance, we have obtained the kinetic parameters for thermolysis for a phase whose crystal sizes are substantially smaller than the minimal size after self-dispersal of a block of a large crystal (0.5–2 m). For thermolysis of the hemiaquo adduct not accompanied by self-dispersal, the kinetic characteristics of the process for phases of dispersity 0.5–2 mm and 0.5–2 m are comparable.Translated from Teoreticheskaya i Éksperimental'naya Khimiya, Vol. 28, No. 3, pp. 226–231, May–June, 1992. 相似文献
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Budarin VL Clark JH Tavener SJ Wilson K 《Chemical communications (Cambridge, England)》2004,(23):2736-2737
The reaction of localised C[double bond, length as m-dash]C bonds on the surface of activated carbons has been shown to be an effective method of chemical modification especially using microwave-assisted reactions. 相似文献
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Aleksandra Borisova Mario De Bruyn Vitaliy L. Budarin Peter S. Shuttleworth Jennifer R. Dodson Mateus L. Segatto James H. Clark 《Macromolecular rapid communications》2015,36(8):774-779
Bio‐derived polysaccharide aerogels are of interest for a broad range of applications. To date, these aerogels have been obtained through the time‐ and solvent‐intensive procedure of hydrogel fomation, solvent exchange, and scCO2 drying, which offers little control over meso/macropore distribution. A simpler and more versatile route is developed, using freeze drying to produce highly mesoporous polysaccharide aerogels with various degrees of macroporosity. The hierarchical pore distribution is controlled by addition of different quantities of t‐butanol (TBA) to hydrogels before drying. Through a systematic study an interesting relationship between the mesoporosity and t‐butanol/water phase diagram is found, linking mesoporosity maxima with eutectic points for all polysaccharides studied (pectin, starch, and alginic acid). Moreover, direct gelation of polysaccharides in aqueous TBA offers additional time savings and the potential for solvent reuse. This finding is a doorway to more accessible polysaccharide aerogels for research and industrial scale production, due to the widespread accessibility of the freeze drying technology and the simplicity of the method.
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V. E. Diyuk A. A. Gorlova V. L. Budarin V. V. Sidorchuk V. K. Yatsimirskii 《Theoretical and Experimental Chemistry》2011,47(3):199-204
We have used the barothermal treatment method (heat and pressure) to modify the surface of activated charcoal with maleic
anhydride. As a result of the modification, about 1 mmol/g of thermally stable carboxyl groups are formed on the surface with
a decomposition temperature range of 330–470°C. We show that the proposed procedure makes it possible to obtain materials
with a uniform coverage of functional groups. 相似文献
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M. R. DE BACKER-BARILLY A. BARBE S. A. TASHKUN VL. G. TYUTEREV A. CHICHERY 《Molecular physics》2013,111(22):3499-3506
The four 5v 3 bands of 18O enriched ozone have been observed and analysed for the first time. Two species (16O18O16O and 18O16O18O) belong to the C2v symmetry group and two other (18O18O16O and 16O16O18O) to the Cs symmetry group. They have been recorded at a resolution of 0.008 cm?1 with a pathlength of 32.16 m. Despite the very weak absorptions observed, almost 250 energy levels have been derived for each of the 4 species, with J ? 35 and K a ? 13, and suitable sets of Hamiltonian parameters have been determined. For 3 species it has been necessary to account for the resonance between the (005) and (311) states to correctly reproduce the spectra observed. These resonances, anharmonic for C2v, and hybrid (both anhar-monic and Coriolis) for Cs symmetry confirm the accidentally extremely strong coupling between the (005) and (311) states for 16O3, due in that case to the very close distance between unperturbed energy levels. This work also confirms the excellent prediction of band centres of these four species derived from the recently determined isotopically invariant molecular potential function. 相似文献
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