Please use this identifier to cite or link to this item: https://hdl.handle.net/10356/99142
Title: Structure and surface reactivity of WO42– , SO42– , PO43– modified Ca-hydroxyapatite catalysts and their activity in ethanol conversion
Authors: Ramesh, Kanaparthi
Goh, Eileen Yi Ling
Gwie, C. G.
White, Timothy John
Borgna, Armando
Issue Date: 2012
Source: Ramesh, K., Goh, E. Y. L., Gwie, C. G., White, T. J., & Borgna, A. (2012). Structure and Surface Reactivity of WO42– , SO42– , PO43– Modified Ca-Hydroxyapatite Catalysts and Their Activity in Ethanol Conversion . The Journal of Physical Chemistry C, 116(35), 18736-18745.
Series/Report no.: The journal of physical chemistry C
Abstract: In the current study, we have synthesized calcium hydroxyapatite (CaHAP) from different phosphorus sources namely, NH4H2PO4 and H3PO4. The structure of CaHAP was confirmed by XRD, FT-IR, and Raman characterization methods. The CaHAP was further modified with various anions such as WO42–, SO42–, and PO43– with fixed content of 10 wt %. To understand the textural and structural properties, these samples were thoroughly characterized by N2 physisorption, X-ray diffraction, Fourier transform infrared, Raman and thermogravimetry–differential thermal analysis methods. Ethanol adsorption at various temperatures was studied in detail using diffuse reflectance Fourier transform spectroscopic to unravel the formation and stability of surface species and the interaction of ethanol with CaHAP. The temperature programmed desorption of ethanol (ethanol-TPD) was performed to understand the stability, surface reactivity, and product distribution. The catalytic activity of the above catalysts was tested in ethanol conversion over a temperature range of 300–450 °C.
URI: https://hdl.handle.net/10356/99142
http://hdl.handle.net/10220/17232
DOI: 10.1021/jp304187v
Fulltext Permission: none
Fulltext Availability: No Fulltext
Appears in Collections:MSE Journal Articles

Google ScholarTM

Check

Altmetric

Items in DR-NTU are protected by copyright, with all rights reserved, unless otherwise indicated.