Impact of Al2O3 Particle Size on the Open Porosity of Ni/Al2O3 Composites Prepared by the Thermal Oxidation at Moderate Temperatures

The performance of attractive Ni-based composites can be affected by changing their microstructures, e.g., introducing pores. Here, we report a novel, relatively low-cost process to fabricate Ni/Al2O3 composites with open porosity modified by the size of Al2O3 particles. The mixture of powders was subjected to thermal oxidation twice in air after a maximal temperature of 800 °C was reached in a stepwise manner and maintained for 120 min. The oxidation kinetics were determined thermogravimetrically. The open porosity was evaluated by an Archimedes’ principle-based method. Localization and quantification of NiO, newly formed on the Ni particle surface and acting as a mechanical bonding agent, were explored by scanning electron microscopy with energy dispersive X-ray spectroscopy and X-ray diffractometry. Larger ceramic particles prevented merging of NiO layers on adjacent Ni particles more efficiently; therefore, the open porosity increased from 21% to 24.2% when the Al2O3 particle diameter was increased from 5–20 µm to 32–45 µm. Because both Ni/Al2O3 composites exhibited similar flexural strength, the composite with larger Al2O3 particles and the higher open porosity could be a better candidate for infiltration by molten metal, or it can be directly used in a variety of filtration applications

Properties of a new calcium-permeable single channel from tracheal microsomes

AbstractAfter the incorporation of the tracheal microsomal membrane into bilayer lipid membrane (BLM), a new single channel permeable for calcium was observed. Using the BLM conditions, 53 mM Ca2+ in trans solution versus 200 nM Ca2+ in cis solution, the single calcium channel current at 0 mV was 1.4–2.1 pA and conductance was 62–75 pS. The channel Ca2+/K+ permeability ratio was 4.8. The open probability (P-open) was in the range of 0.7–0.97. The P-open, measured at −10 mV to +30 mV (trans-cis), was not voltage dependent. The channel was neither inhibited by 10–20 μM ruthenium red, a specific blocker of ryanodine calcium release channel, nor by 10–50 μM heparin, a specific blocker of IP3 receptor calcium release channel, and its activity was not influenced by addition of 0.1 mM MgATP. We suggest that the observed new channel is permeable for calcium, and it is neither identical with the known type 1 or 2 ryanodine calcium release channel, nor type 1 or 2 IP3 receptor calcium release channel