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Porous geopolymer precursors were firstly prepared by the direct foaming method using bauxite, fly ash (FA), and metakaolin (MK) as raw materials, and porous mullite ceramics were prepared after ammonium ion exchange and then high-temperature sintering. The effects of chemical foaming agent concentration, ion-exchange time, and sintering temperature on porous geopolymer-derived mullite ceramics were studied, and the optimal preparation parameters were found. Studies have shown that the concentration of blowing agent had great influence on open porosity (q) and porosity and cell size distributions of geopolymer samples, which in turn affected their compressive strength (σ). Duration of the ion exchange had no obvious effect on the sintered samples, and the amount of mullite phase increased with the increase in the sintering temperature. Mullite foams, possessing an open-celled porous structure, closely resembling that of the starting porous geopolymers produced by directly foaming, were obtained by firing at high temperatures. Stable mullite (3Al2O3·2SiO2) ceramic foams with total porosity (ε) of 83.52 vol%, high open porosity of 83.23 vol%, and compressive strength of 1.72 MPa were produced after sintering at 1400 ℃ for 2 h in air without adding any sintering additives using commercial MK, bauxite, and FA as raw materials.


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Open-cell mullite ceramic foams derived from porous geopolymer precursors with tailored porosity

Show Author's information Jiahuan ShaoaChengying Baia( )Xinyu Lia( )Kun YangaTing ZhengaYingjie QiaoaLili ZhangaHongqiang LibPaolo Colomboc,d
Key Laboratory of Superlight Materials and Surface Technology, Ministry of Education, College of Materials Science and Chemical Engineering, Harbin Engineering University, Harbin 150001, China
College of Civil Engineering, Hunan University, Changsha 410082, China
Department of Industrial Engineering, University of Padova, via Marzolo, Padova 35131, Italy
Department of Materials Science and Engineering, The Pennsylvania State University, State College 16802, USA

Abstract

Porous geopolymer precursors were firstly prepared by the direct foaming method using bauxite, fly ash (FA), and metakaolin (MK) as raw materials, and porous mullite ceramics were prepared after ammonium ion exchange and then high-temperature sintering. The effects of chemical foaming agent concentration, ion-exchange time, and sintering temperature on porous geopolymer-derived mullite ceramics were studied, and the optimal preparation parameters were found. Studies have shown that the concentration of blowing agent had great influence on open porosity (q) and porosity and cell size distributions of geopolymer samples, which in turn affected their compressive strength (σ). Duration of the ion exchange had no obvious effect on the sintered samples, and the amount of mullite phase increased with the increase in the sintering temperature. Mullite foams, possessing an open-celled porous structure, closely resembling that of the starting porous geopolymers produced by directly foaming, were obtained by firing at high temperatures. Stable mullite (3Al2O3·2SiO2) ceramic foams with total porosity (ε) of 83.52 vol%, high open porosity of 83.23 vol%, and compressive strength of 1.72 MPa were produced after sintering at 1400 ℃ for 2 h in air without adding any sintering additives using commercial MK, bauxite, and FA as raw materials.

Keywords: porosity, direct foaming, porous mullite ceramic, porous geopolymer precursor, nanophase strengthening

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Received: 14 July 2022
Revised: 23 September 2022
Accepted: 18 October 2022
Published: 10 January 2023
Issue date: February 2023

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© The Author(s) 2022.

Acknowledgements

This work was supported by the National Natural Science Foundation of China (52002090), the Heilongjiang Postdoctoral Science Foundation Funded Project (LBH-Z19051), the Fundamental Research Funds for the Central Universities (XK21000210), the Scientific Research Foundation for the Returned Overseas Chinese Scholars of Heilongjiang Province (2019QD0002), and the open fund from Key Laboratory of Superlight Materials and Surface Technology, Ministry of Education (XK2100021044).

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