Abstract
Tin(IV) oxide catalysts, pure and surface-doped with different loading levels of sulfate, have been prepared and characterized by means of thermal analysis (TGA and DTA), X-ray powder diffraction (XRD), nitrogen adsorption at 77 K, FT-IR spectroscopy using KBr pellets and potentiometric titration using n-butylamine. The catalysts were prepared from aqueous solutions of ammonia and tin(IV) chloride, with production of an amorphous precipitate that calcined at 873 K for 3 h to give tin(IV) oxide (SnO 2). The sulfation was carried out by impregnation of sulfuric acidic 0.5 M with tin(IV) hydroxide with different amounts of sulfate (6%, 12% and 18% SO 4 - 2 by weight). Structural investigation of the catalysts by TGA, XRD and N 2-sorption revealed that tin(IV) gel has at least two molecules of water to give the formula SnO 2·2H 2O and the addition of sulfate does not modify the crystalline structure of tin(IV) oxide (tetragonal phase) but decreases the crystallite size and, consequently, increase the specific surface area. The increase in loading level of sulfate resulted in increase in specific surface area of the catalysts. Acidity measurement by potentiometric titration using n-butylamine show that the addition of sulfate can increase the acidity of tin(IV) oxide and all sulfated tin(IV) oxide having strong acid sites. Moreover, FT-IR spectra expose that sulfated tin(IV) oxide has two different structures of sulfates.
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
More From: Journal of the Association of Arab Universities for Basic and Applied Sciences
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.