Experimental study on the effects of sediment size and porosity on contaminant adsorption/desorption and interfacial diffusion characteristics

The joint effects of the sediment size and porosity on the contaminant adsorption/desorption and interfacial diffusion characteristics were experimentally investigated. The adsorption of Phosphorus （P） on the natural and artificial sediment suspensions was measured with respect to the P adsorption isotherms and kinetics in the experiment. The obtained adsorption isotherms for different grain-sized sediment suspensions fit well with the Langmuir equation, dependent on the initial aqueous concentration and sediment content. The P kinetic adsorption behaviors for cohesive fine-grained and non-cohesive coarse-grained sediment suspensions clearly show the size-dependent feature. On the other hand, the P kinetic release feature of a porous sediment layer is affected by not only the direct desorption of the uppermost sediments, but also the diffusivity in the pore-water within the underlying sediment layer, characterized by the sediment size and porosity, respectively. Furthermore, the temporal contaminant release from the permeable sediment layer into the overlying water column increases with the increasing flow velocity, while this enhancement in mediating the interfacial diffusion flux is somewhat insignificant in an immediate release stage, largely due to the resistance of the diffusive boundary layer on the hydrodynamic disturbance.

The effect of interfacial diffusion on device performance of polymer solar cells: a quantitative view by active-layer doping

The diffusion of constituent materials at interfaces is one of the key factors for device performance and stability. In this work, the effect of interfacial diffusion of a classic interfacial material PFN on device performance of polymer solar cells was studied quantitatively by doping PFN into active layer based on P3HT：PC61BM blend. The PCEs of devices with 550 ppm PFN de- crease to half compared to those of the control devices without PFN, which are mainly attributed to the decrease of short-circuit current （Jsc） and fill factor （FF）. Advanced analyses of equivalent circuit, absorption spectra, and atomic force mi- croscopy indicates that the presence of PFN in the active layer increases the leakage current, decreases the aggregation of P3HT, and reduces the phase separation. This research reveals the physical mechanism of interfacial diffusion in device per- forrnance and provides a basis for further improving the performance and stability of PSCs.

THEORETICAL PREDICTION OF PROEUTECTOID FERRITICTRANSFORMATION IN HYPO-PROEUTECTOID STRUCTRAL STEELS

Proeutectoid ferrite with carbon content xo precipitating from austenite in a multicomponent steel at temperature T is supposed to be equivalent to proeutectoid ferrite with the same carbon content precipitating from austenite in Fe-C binary system at temperature T'.is described as the temperature difference of proeutectiod ferrite formation, and can be calculated from the Fe-X diagrams and the equilibrium temperature A3. By introducing Tf and basing on the thermodynamic model for Fe-C binary alloy, the driving force for phase transformation from austenite to proeutectoid ferrite in multicomponent steels has been successfully calculated. Through the Johnson-Mehl equation and using the data hem known TTT diagrams, the relationship between the chemical composition and the intedecial edenly packeter as well as activation energy for proeutectoid ferrite formation can be calculated. The starting curves of proeutectoid ferritic transformation calculated in this way in some hypo-proeutectoid structural steels agree well with the erperimental data.