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Pressure Dependencies (pressure + dependency)
Selected AbstractsA temperature-dependent kinetics study of the reaction of O(3PJ) with (CH3)2SOINTERNATIONAL JOURNAL OF CHEMICAL KINETICS, Issue 3 2002F. D. Pope A laser flash photolysis,resonance fluorescence technique has been employed to investigate the kinetics of the reaction of ground state oxygen atoms, O(3PJ), with (CH3)2SO (dimethylsulfoxide) as a function of temperature (266,383 K) and pressure (20,100 Torr N2). The rate coefficient (kR1) for the O(3PJ) + (CH3)2SO reaction is found to be independent of pressure and to increase with decreasing temperature. The following Arrhenius expression adequately describes the observed temperature dependence: kR1(T) = (1.68 ± 0.76) × 10,12 exp[(445 ± 141)/T] cm3 molecule,1 s,1, where the uncertainties in Arrhenius parameters are 2, and represent precision only. The absolute accuracy of each measured rate coefficient is estimated to be ±30%, and is limited predominantly by the uncertainties in measured (CH3)2SO concentrations. The observed temperature and pressure dependencies suggest that, as in the case of O(3PJ) reactions with CH3SH and (CH3)2S, reaction occurs by addition of O(3PJ) to the sulfur atom followed by rapid fragmentation of the energized adduct to products. The O(3PJ) + (CH3)2SO reaction is fast enough so that it could be a useful laboratory source of the CH3SO2 radical if this species is produced in significant yield. © 2002 Wiley Periodicals, Inc. Int J Chem Kinet 34: 156,161, 2002; DOI 10.1002/kin.10040 [source] Pressure Dependence of Exchange Parameters and Neel Temperature in La2CuO4ISRAEL JOURNAL OF CHEMISTRY, Issue 3-4 2007Anatolii Ya. Microscopic mechanisms responsible for the observed pressure dependencies of the Neel temperature TN and parameters of isotropic and anisotropic exchange interaction in the orthorhombic antiferromagnet La2CuO4 are investigated. Within the framework of the Anderson microscopic theory of superexchange interaction, the expressions establishing interrelation between parameters of isotropic and anisotropic (both symmetric and antisymmetric) exchange interactions and by the structural parameters describing the Cu-O-Cu bonding angle and the Cu-O bond length in La2CuO4 are obtained. Experimentally determined pressure dependencies of structural parameters by H. Takahashi et al., allow one to present pressure dependencies of exchange parameters and TN in an apparent form. [source] Sorption and permeation behavior for CO2 in NH3 -plasma-treated and untreated polystyrene membranesJOURNAL OF APPLIED POLYMER SCIENCE, Issue 3 2007Y.-S. Yang Abstract In our preceding work, the simultaneous deviation from the conventional dual-mode sorption and mobility model was observed in a case of CO2 in polystyrene (PS) membrane (glass transition temperature of pure polymer = 95°C) at 60 and 70°C. The plasticization effect of sorbed CO2 on both the sorption and diffusion processes tends to be brought about in glassy polymer membranes near the glass transition temperature. The behavior was simulated based on the concept that only one population of sorbed gas molecules of plasticizing ability to the polymer should exist. In the present work, the sorption and permeation behavior for CO2 in NH3 -plasma-treated and untreated PS membranes at 40°C was investigated, where NH3 -plasma treatment was executed at plasma discharge powers of 40, 80, 120, and 160 W for an exposure time of 2 min. The sorption isotherm could be described by the sorption theory of Mi et al. (Macromolecules 1991, 24, 2361), where the glass transition temperature is depressed by a concentration of sorbed CO2 of plasticizing ability. NH3 -plasma treatment on PS membrane had little influence on the sorption behavior of CO2 at plasma discharge powers up to 160 W. The mean permeability coefficients were somewhat increased only at a discharge power of 160 W. At CO2 pressures below 0.9 MPa, the pressure dependencies of mean permeability coefficients for CO2 in both NH3 -plasma-treated and untreated PS membranes at 40°C could also be simulated on the basis of the concept that only one population of sorbed gas molecules of plasticizing ability should exist. At CO2 pressures above 0.9 MPa, however, a plasticization action of sorbed CO2 had much more influence on the diffusion process rather than on the sorption one, and such a combined concept underestimated the mean permeability coefficient. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 103: 1798,1805, 2007 [source] | ||||||||||