Preparation of catalyst from phosphorous rock using an improved wet process for transesterification reaction

Abstract

Gypsum (CaSO4·2H2O) with active catalytic performance was prepared from phosphorous rock through an improved clean wet process. The impact of the preparation conditions was extensively analyzed to identify the statistical significance toward the compositions of the prepared gypsum and catalytic performances during the transesterification reaction. The prepared catalyst predominantly contains CaSO4 (93%) with contaminations of silica (5%), P2O5 (0.25%), Fe2O3 (0.52%), Al2O3 (0.24%), and TiO2 (0.12%). Heavy-metal oxides, that is, Cr2O3, PbO, and CuO, were not detected from the prepared catalyst. The contaminants in gypsum are in the form of complicated composites such as SiO2, (Na2, K2)SiF6, MgF2, AlF3, Ca5(PO4)3F, and Ca3(PO4)2. The significant operational parameters, namely, the crystallization temperature and duration toward the catalytic performance, were identified by ANOVA. The Brönsted acidic sites from the ionic S and O, which might be in the form of S-⃛O or S═O as the surface functional groups, attribute to transesterification catalysis. The theoretical simulation suggests that different ionic sulfates might co-exist on the surface of crystallite gypsum. The transport of reagents to the surface of catalytic sites also plays an important role under the investigated experimental conditions. The reusability study indicates an approximate 10% deactivation after the reaction.

RAS ID

39622

Document Type

Journal Article

Date of Publication

2021

Funding Information

Funding information : https://doi.org/10.1021/acs.iecr.1c01072

School

School of Engineering

Copyright

subscription content

Publisher

ACS

Comments

Wang, Y., Tang, M., Yusuf, A., Wang, Y., Zhang, X., Yang, G., ... Sun, Y. (2021). Preparation of catalyst from phosphorous rock using an improved wet process for transesterification reaction. Industrial & Engineering Chemistry Research, 60(22), 8094-8107. https://doi.org/10.1021/acs.iecr.1c01072

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Link to publisher version (DOI)

10.1021/acs.iecr.1c01072