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41.
E. Ya. Davydov I. S. Gaponova T. V. Pokholok G. B. Pariiskii G. E. Zaikov 《应用聚合物科学杂志》2008,108(1):128-133
The features of initiation of free radical reactions in polymers by dimers of nitrogen dioxide are considered. The conversion of planar dimers into nitrosyl nitrate in the presence of amide groups of macromolecules has been revealed. Nitrosyl nitrate initiates radical reactions in oxidative primary process of electron transfer with formation of intermediate radical cations and nitric oxide. As a result of subsequent reactions, nitrogen‐containing radicals are produced. The dimer conversion has been exhibited by estimation of the oxyaminoxyl radical yield in characteristic reaction of p‐benzoquinone with nitrogen dioxide on addition of aromatic polyamide and polyvinylpyrrolidone to reacting system. The isomerization of planar dimers is efficient in their complexes with amide groups, as confirmed by ab initio calculations. © 2007 Wiley Periodicals, Inc. J Appl Polym Sci, 2008 相似文献
42.
Anodic oxidation of mecoprop herbicide at lead dioxide 总被引:1,自引:0,他引:1
The electrochemical oxidation of an aqueous solution containing mecoprop (2-(2-methyl-4-chlorophenoxy)propionic acid) has
been studied at PbO2 anodes by cyclic voltammetry and bulk electrolysis. The influence of current density, hydrodynamic conditions, temperature
and pH on the degradation rate and current efficiency is reported. The results obtained show that the use of PbO2 leads to total mineralization of mecoprop due to the production of oxidant hydroxyl radical electrogenerated from water discharge.
The current efficiency for the electro-oxidation of mecoprop is enhanced by low current density, high recycle flow-rates and
high temperature. In contrast, the pH effect was not significant. It has also been observed that mecoprop decay kinetics follows
a pseudo-first-order reaction and the rate constant increases with rising current density. 相似文献
43.
44.
Erdogan Kiran 《Polymer》2008,49(7):1853-1859
Morphological changes that take place in poly(?-caprolactone) upon exposure to carbon dioxide at high pressures have been explored as a function of pressure and temperature. SEM and DSC results point to a competition between CO2-modulated crystallization and pressure-induced phase separation which leads to unique morphologies. At 293 K, exposure to CO2 at pressures up to 45 MPa leads to recrystallization resulting in higher level of crystallinity and higher melting temperatures. Highest crystallinity levels along with distinct crystal morphology were observed after exposure to CO2 at 308 K and 21 MPa. At a higher pressure at this temperature (308 K/34 MPa) polymer undergoes melting, and foaming is achieved during depressurization prior to solidification. At 323 K, the polymer is found to display unique crystal morphology with concave crystal geometry as well as porous domains. The results are discussed in terms of the crystallization and phase separation paths that are followed during exposure to CO2 and the depressurization stages. 相似文献
45.
研究了不同热处理温度和不同测试温度下,纳米CeO2基薄膜的电性能.结果表明,纳米CeO2基薄膜在热处理温度为600℃和900℃时,其伏安特性曲线近似为线性特征;在热处理温度为700℃和800℃时,其伏安特性曲线中存在VCNR现象.结合纳米CeO2基薄膜的XRD图,对纳米CeO2基薄膜的电性能进行了理论分析和讨论. 相似文献
46.
G. Scalabrin L. Piazza M. Condosta 《International Journal of Heat and Mass Transfer》2003,46(23):4413-4425
In a previous work, convective heating of carbon dioxide was studied with neural networks (NN), obtaining a totally heuristical heat transfer equation from the direct regression of experimental data. In the present work, the analysis focuses on the cooling process, which has a technical relevance in various applications, as for example in transcritical refrigeration cycles. Heat transfer around the critical zone presents a marked enhancement, that follows the peaks in thermophysical properties like thermal conductivity and heat capacity. Similarly, other properties like density and enthalpy, present a strong variation in narrow temperature intervals around the critical point.This constitutes then a highly non-linear phenomenon, for which it is advisable to use a very flexible function approximator like the NNs. NN models were applied both in terms of dimensionless numbers and of physical quantities, obtaining the two corresponding NN architectures. The choice of the optimal number of neurons in the NN hidden layer is discussed. The NN models are then compared with a recent correlation from literature, for which the validation results present an AAD of 27% and a bias of −26% with an evident prediction shifting. On the other hand the NN models in terms of dimensionless numbers and of physical quantities have AAD and bias of 14% and −4%, and of 7% and −2%, respectively, showing a largely better performance. 相似文献
47.
用二氧化硫法处理贫软锰矿,得到含硫酸锰和连二硫酸锰的溶液,继而将该溶液进行净化,除杂,浓缩,结晶处理即得工业级硫酸锰,结晶母液用碳铵沉淀即得碳酸锰产品 相似文献
48.
David Lloyd Suzie Morrell Helle N. Carlsen Hans Degn Phillip E. James Christopher C. Rowlands 《Yeast (Chichester, England)》1993,9(8):825-833
Saccharomyces cerevisiae HSc was grown with ethanol at concentrations up to 10% (v/v). The immediate effects of additions of externally added ethanol on CO2 production and O2 consumption of washed organisms were studied by stopped-flow membrane inlet quadrupole mass spectrometry. Fermentative activities of organisms grown with ethanol (0–5% v/v) showed similar sensitivities to inhibition by ethanol, whereas those grown with 10% (v/v) ethanol had become protected and were markedly less sensitive. The fluidity of subcellular membrane fractions was measured by determination of the temperature dependence of the rotational order parameter of the spin label 5-doxyl stearic acid (free radical) by electron spin resonance. Mitochondria prepared from yeasts grown with 0, 7 and 9% (v/v) ethanol showed similar overall fluidity, although differences in temperature-dependent behaviour indicate altered lipid composition or lateral phase separations. On the other hand the microsomal fraction from organisms grown with 9% ethanol showed a remarkable increase in fluidity. These data suggest that the protective effects of growth with ethanol near the limit of tolerance on fermentative activities may arise from altered plasma membrane fluidity properties. 相似文献
49.
Forest and bioenergy strategies offer the prospect of reduced CO2 emissions to the atmosphere. Such strategies can affect the net flux of carbon to the atmosphere through 4 mechanisms: storage of C in the biosphere; storage of C in forest products; use of biofuels to displace fossil-fuel use; use of wood products which often displaces other products that require more fossil fuel for their production. We use the mathematical model GORCAM (Graz/Oak Ridge Carbon Accounting Model) to examine these mechanisms for 16 land-use scenarios. Over long time intervals the amount of C stored in the biosphere and in forest products reaches a steady state and continuing mitigation of C emissions depends on the extent to which fossil fuel use is displaced by the use of bioenergy and wood products. The relative effectiveness of alternative forest and bioenergy strategies and their impact on net C emissions strongly depend, for example, on the productivity of the site, its current usage, and the efficiency with which the harvest is used. When growth rates are high and harvest is used efficiently, the dominant opportunity for net reduction in C emissions is seen to be fossil-fuel displacement. At the growth rates and efficiencies of harvest utilization adopted in many of our base scenarios, the net C balance at the end of 100 years is very similar whether trees are harvested and used for energy and traditional forest products, or reforestation and forest protection strategies are implemented. The C balance on a plantation system that provides a constant output of biomass products can look different than the balance of a single parcel of land. 相似文献
50.
Zakaria Chajar Michel Primet Hélène Praliaud Michèle Chevrier Catherine Gauthier Frédéric Mathis 《Catalysis Letters》1994,28(1):33-40
The role of nitrogen dioxide in the selective reduction of NO by propane over a Cu-MFI zeolite is investigated. NO2 and NO reductions were carried out under similar conditions of reaction. In the presence of oxygen, the reduction of NO by C3H8 does not differ significantly from that of NO2. In the absence of oxygen, the reduction of NO2 by propane occurs with a partial decomposition of the nitric dioxide molecule. Such a decomposition leads to the formation of oxygen, which is responsible for the increase in catalytic activity by comparison with the same reaction performed with NO. NO2 formed and released in the gas phase during the reduction of NO by propane in the presence of oxygen does not play a predominant role in the catalytic process. 相似文献