Abstract

In this work, we report the preparation, structural and electrical characterization, morphological analysis and hardness measurements of ceramic materials composed of kaolinite Al2(Si2O5(OH)4 and alumina AL2O3. Samples were prepared from mixtures of precursor oxides starting with 100% alumina and increased the kaolinite concentration on steps of 10% up to complete 100% of kaolinite. The samples were sintered by the method of solid state reaction at temperatures of 1150, 1250 and 1350 °C. We found that the alumina samples are stable at the different temperatures of synthesis. The samples of kaolinite at 100% suffer a change phase depending on the sinterization temperature, noting that at 1350 °C yields 87% mullite and 13% cristobalite. The presence of quartz was only detected in samples with 100% kaolinite for sinterization temperatures of 1150 and 1250 °C. All samples with a mixture of alumina and kaolinite showed the presence of mullite, which is increased when the content of kaolínite is high or when the sinterization temperature is increased. This allows us to infer that the introduction of alumina optimizes the process of mullite formation hy their reaction with the SiO2 that remainder from the kaolinite. The sample with 100% alumina has a Mohs hardness of about 5, and this is increased with the content of kaolinite, until a Mohs hardness of about 6 to the sample with 100% kaolinite. The dielectric constant of these materials is around 27.82.

Full Text
Paper version not known

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.