85
Views
0
CrossRef citations to date
0
Altmetric
Article

Nanocrystalline La0.84Sr0.16MnO3 and NiO-YSZ by Combustion of Metal Nitrate-Citric Acid/Glycine Gel – Phase Evolution and Powder Characteristics

, , , , , , & show all
Pages 182-190 | Received 07 Nov 2012, Accepted 03 May 2013, Published online: 07 Oct 2013
 

Abstract

Phase evolution behaviour of lanthanum strontium manganite (LSM) and nickel oxide-yttria stabilized zirconia (NiO-YSZ) composite from the respective oven dried fuel – metal nitrate gels (citrate-metal nitrate for LSM and glycine-metal nitrate for NiO-YSZ) was studied using TG-DTA, XRD and FTIR. The TG-DTA revealed sharp exotherms around 200° and 221°C attributed to the setting in of combustion of gels of LSM and NiO-YSZ respectively. The XRD results indicated formation of nanocrystalline LSM and NiO-YSZ phases above 200° and 221°C respectively. The FTIR spectra of LSM and NiO-YSZ gels heated above 200° and 221°C exhibited characteristic absorption bands corresponding to metal-oxygen vibrations in LSM and NiO-YSZ indicating formation of the respective compounds. However, chemical and phase pure LSM and NiO formed above 700°C indicate the minimum calcination temperature to be used in the processing. The role of calcination treatment on powder characteristics in the temperature range of 700° to 1350°C was studied. With increasing calcination temperature of the as-formed powders, the characteristics such as crystallite size, median particle size (D50), green density of the compacts increased while specific surface area decreased. Typical sintering studies at 1400° and 1450°C revealed that sinterability and per cent linear shrinkage decreased with increasing calcination temperature. However, the required amount of porosity for SOFC application could be obtained with incorporation of a pore former in case of LSM and varying the sintering time in case of NiO-YSZ composite.

Reprints and Corporate Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

To request a reprint or corporate permissions for this article, please click on the relevant link below:

Academic Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

Obtain permissions instantly via Rightslink by clicking on the button below:

If you are unable to obtain permissions via Rightslink, please complete and submit this Permissions form. For more information, please visit our Permissions help page.