The balance calculation of zinc and lead of No.1 BF of Baotou Iron and Steel Group Co. was performed in this research. The particle sizes of BF dusts were measured by LS230 laser particle size analyzer. The micrology of sinter and dusts were investigated with scanning electron microscopy (SEM, Hitachi S-3000) coupled with an energy-dispersive X-ray analysis (EDX). The results show that the general burdens of zinc and lead in No. 1 mainly came from sinter and pellet. The burdens of zinc and lead in No.1 BF were 645.45g/t and 370.33 g/t respectively, which were too much to need take some measures. Among the gas ash, the particle size of baghouse dust was minimal, but the contents of lead and zinc were highest. So the BF baghouse dust isn’t appropriate to recover as the sintering materials. The speciation of lead is PbO, PbCl3 and metallic Pb, but zinc never presents as metal in BF dusts.
A new method based on a solution graft technique was used to prepare poly (vinylidene fluoride) grafted polystyrene sulfonated acid (PVDF-g-PSSA) proton exchange membrane. Polystyrene is grafted into PVDF modified by plain sodium silicate (Na4SiO4). There is a linear relationship between the degree of grafting and the content of Na4SiO4. Fourier transform infrared spectroscopy is used to characterize changes of the membrane's microstructures after grafting and sulfonation. The morphology of the membrane's microstructures after grafting and sulfonation is studied by scanning electrolytic microscope (SEM). The effect of plain sodium silicate (Na4SiO4) concentration and relative humidity on the conductivity of the electrolyte was investigated by the impedance at room temperature. The results show that the styrene has been grafted into PVDF. The conductivity of PVDF-g-PSSA electrolyte doped 10% plain sodium silicate (Na4SiO4) is 0.016 S/cm at room temperature. The conductivity of the electrolyte changes slightly at a relative humidity range of 20%-70%. The weightlessness of PVDF-g-PSSA electrolyte heated to 40°C was less than 2%, which indicated that water capacity was good.
A proton exchange membrane of poly (vinylidene fluoride) grafted onto poly (2-acrylamido-2-methylpropane sulfonic acid) (PVDF-g-PAMPS) was prepared as follows: acrylamido-2-methylpropane sulfonic acid (AMPS) was first added to a N-Methyl pyrrolidone (NMP) solution containing poly (vinylidene fluoride) (PVDF) that was modified with plain sodium silicate. Ammonium persulfate was then added as an evocating agent and PAMPS was directly grafted onto the PVDF that was modified with plain sodium silicate. The influences of AMPS contents on the proton conductivity and mechanical properties were studied. The results showed that AMPS is easily grafted into PVDF modified by Plain sodium silicate (Na4SiO4) and mechanical properties were improved, with increasing of the content of 2-acrylamido-2-methylpropane sulfonic acid, the proton conductivity of PVDF-g-PAMPS membranes was increased.
A proton exchange membrane of blended poly (acrylamido-2- methylpropane sulfonic acid) (PAMPS) grafted onto modified poly (vinylidene fluoride) (PVDF) membrane (PVDF-g-PAMPS) was prepared. Fourier transform infrared spectroscopy is used to characterize changes of the membrane's microstructures after grafting. The morphology of the membrane's microstructures after grafting is studied by scanning electrolytic microscope.The results show that 2-acrylamido-2-methylpropane sulfonic acid is easily grafted into PVDF modified by Plain sodium silicate (Na4SiO4).
Cu-based anode has no or little catalytic activity to reaction of precipitating carbon during using carbon-hydrogen fuel, which can avoid failure or disintegration of SOFC caused by catalytically precipitating carbon resulting from Ni-based anode. However, the melting point of CuO, that is 1148°C, is far below the sintering temperature of electrolyte which limits the use of Cu-based anode. So the property of sintering of Cu-based anode between 1050°C and 1150°C was studied by co-pressing and co-sintering Cu-based anode with electrolyte. The result shows that the diffusion of copper in the electrolyte is not apparent when the co-sintering temperature is below 1130°C. At 1140°C, the Matano plane moved to anode side and the diffusion coefficient of copper in the electrolyte is relevant to concentration of copper which is 0.543×10-8-1.74×10-8(cm2•s-1) when the content of copper is 1.51%~18.7%.
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