Kinetics Study on O2 Adsorption and OHad Desorption at Pt（111）, Its Implication to Oxygen Reduction Reaction Kinetics

Kinetics of dissociative O2 adsorption, OHad desorption, and oxygen reduction reaction （ORR） at Pt（111） electrode in 0.1 mol/L HClO4 has been investigated. Reversible OHad adsorption/desorption occurs at potentials from 0.6 V to 1.0 V （vs. RHE） with the exchange current density of ca. 50 mA/cm^2 at 0.8 V, the fast kinetics of OHad desorption indicates that it should not be the rate determining step for ORR. In the kineticor kinetic-mass transport mix controlled potential region, ORR current at constant potential displays slight decrease with reaction time. ORR current in the positive-going potential scan is slightly larger than that in the subsequent negative-going scan with electrode rotation speed （〉800 r/min） and slow potential scan rate （〈100 mV/s）. The open circuit potential of Pt/0.1 mol/L HClO4 interface increases promptly from 0.9 V to 1.0 V after switch from O2 free- to O2-saturated solution. The increase of open circuit potential as well as ORR current decays under potential control due to the accumulation of OHad from dissociative adsorption of O2. It indicates that at Pt（111） the net rate for O2 decomposition to OHad is slightly faster than that for OHad removal, one cannot simply use the assumption of rate determining step to discuss ORR kinetics. Instead, the ORR kinetics is determined by both the kinetics for O2 decomposition to OHad as well as the thermo-equilibrium of OHad＋H^＋＋e→←H2O.

The Soret and Dufour Effects in Non-thermal Equilibrium Packed Beds with Forced Convection and Endothermic Reactions＊

To study the influence of the Soret and Dufour effects on the reactive characteristics of a porous packed bed with endothermic reactions and forced convection, a two-dimensional mathematical model considering the cross-diffusion effects was developed in accordance with the thermodynamics of irreversible processes and the local thermal non-equilibrium model. The simulation results were validated by comparing with experimental data. The influence of the Soret and Dufour effects on the heat transfer, mass transfer and endothermic chemical reaction in the non-thermal equilibrium packed bed is discussed. It was found that when the Peclet number reaches 1865, the maximum relative error of the concentration of gas product induced by the Soret effect is 34.7% and that of the solid fractional conversion caused by the Dufour effect is 10.8% at reaction time 160 s and initial temperature 1473 K. The differences induced by the Soret and Dufour effects are demonstrated numerically to increase gradually with the initial temperature of feeding gas and the Peclet number.

Impact of cold indoor thermal environmental conditions on human thermal response

To explore the thermal responses under the non-thermal equilibrium cold environmental conditions,a laboratory study was conducted in climate chamber.The local skin temperatures and thermal sensation of 20 subjects were recorded at 10 min intervals for 90 min under air temperatures of 7.4,9.1,11 and 15 °C.The results show that both local skin temperatures and mean skin temperature decrease not only with the drop of ambient air temperature but also with the exposure time.Local thermal sensation and overall the thermal sensation have the similar temperature-varying and time-varying characteristics.Predicted mean vote(PMV) model cannot correctly predict the thermal sensation under non-thermal equilibrium cold environment.The correlation between local thermal sensation and local skin temperatures shows that thermal sensation is closely related to skin temperature.Skin temperature is an effective indicator of thermal sensation.A linear relationship model between overall thermal sensation and mean skin temperature,considering both ambient temperature and exposure time,was established in the non-thermal equilibrium cold environment,which makes the evaluation of thermal sensation more objective.

Hydrogenation reaction characteristics and properties of its hydrides for magnetic regenerative material HoCu_2

The hydrogenation reaction characteristics and the properties of its hydrides for the magnetic regenerative material HoCu_2(CeCu_2-type) of a cryocooler were investigated. The XRD testing reveals that the hydrides of HoCu_2 were a mixture of Cu, unknown hydride Ⅰ, and unknown hydride Ⅱ. Based on the PCT(pressure-concentration-temperature) curves under different reaction temperatures, the relationships among reaction temperature, equilibrium pressure, and maximum hydrogen absorption capacity were analyzed and discussed. The enthalpy change ΔH and entropy change ΔS as a result of the whole hydrogenation process were also calculated from the PCT curves. The magnetization and volumetric specific heat capacity of the hydride were also measured by SQUID magnetometer and PPMS, respectively.

Effect of hydrogen combustion reaction on the dehydrogenation of ethane in a fixed-bed catalytic membrane reactor

A two-dimensional non-isothermal mathematical model has been developed for the ethane dehydrogenation reaction in a fixed-bed catalytic membrane reactor. Since ethane dehydrogenation is an equilibrium reaction,removal of produced hydrogen by the membrane shifts the thermodynamic equilibrium to ethylene production.For further displacement of the dehydrogenation reaction, oxidative dehydrogenation method has been used.Since ethane dehydrogenation is an endothermic reaction, the energy produced by the oxidative dehydrogenation method is consumed by the dehydrogenation reaction. The results show that the oxidative dehydrogenation method generated a substantial improvement in the reactor performance in terms of high conversions and signi ficant energy saving. It was also established that the sweep gas velocity in the shell side of the reactor is one of the most important factors in the effectiveness of the reactor.

攀枝花钛渣熔盐氯化特性研究

开展了攀枝花74%品位钛渣、78%钛渣和85%钛渣的化学成分、物相及矿物结构研究,考察了三种钛渣熔盐氯化时反应差异、放热量差异和氯化系统热平衡控制差异。研究表明:74%渣、78%渣和85%渣在物相组成上无较大差异,但黑钛石、金红石及其过渡相含量存在差异,导致74%渣熔盐氯化放热量比78%渣多21.9%、85%渣熔盐氯化放热量比78%渣少9.9%,氯化炉热平衡计算所需的返炉矿浆量与实际氯化应用所需矿浆量结果一致。