Ceramics International

All experimental data for all figures represented.

（1) XRD and Raman data (2) Dielectric and ferroelectric data (3)Magnetic data (4)O-Fe-O angle

Excel calculations, raw data, and ImageJ macro from in situ X-ray CT analysis of glass melt.

raw data for all the spectra and thermal imaging

fig.2-a and fig.2-b is MgO and Al2O3 XRD data EDS is the Al2O3/MgO double-layer EDS data Fig1 is the schematic of MgO and Al2O3 atomic layer deposition process

Silica ceramics with opened porosity of 10% was infiltrated with the methyl-phenyl-spirocyclosiloxanol (MPS) acetone solution. Various MPS concentrations in the range of 0.1 – 100% were utilized. The infiltration followed by the polyfunctional condensation to obtain ceramics filled with various volume fractions of the polymethyl-phenyl-spirocyclosiloxane (PMPS). Water absorption capacity, bending strength, dilatometric thermal expansion, optical and structural properties of the obtained materials were analyzed. Water absorption capacity was shown to be less than 0.15% in the range of 1 – 100% MPS fraction in the initial solution. Strength showed logarithmic growth in the range of 45 – 63 MPa with MPS fraction increase. Thermal expansion in comparison to the initial ceramics demonstrated several features that can be correlated to phase transitions and thermal oxidative breakdown of the polymer. Structural properties were analyzed by mercury and gas porometry and spectral scattering technique. Mean size of pores that stay not filled after the infiltration was shown to rise with polymer volume fraction increasing. The obtained results indicate that relatively low fraction of about 1% of the MPS in the initial solution allows one to obtain silica ceramics with low water absorption capacity and sufficient strength. This can be attributed to the polymer tendency to fill predominantly pore throats.

epma results in the CeO2-Sm2O3 System at 1200℃ to 1600℃ in Air

all raw data, images and plots

Data for: Bipolar resistive switching characteristics of PbZrO3/LaNiO3 heterostructure thin films prepared by a sol-gel process

VI characteristics of BN, NiO and BN/NiO nanocomposites