Formation mechanism of high apparent porosity ceramics prepared from fly ash cenosphere

IF 5.8 2区 材料科学 Q2 CHEMISTRY, PHYSICAL Journal of Alloys and Compounds Pub Date : 2018-06-15 DOI:10.1016/j.jallcom.2018.03.303
Feng Jiang , Lingling Zhang , Emile Mukiza , Zhongwei Qi , Daqiang Cang
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引用次数: 26

Abstract

Porous ceramics with high apparent porosity have wide applications in various fields. In this work, high apparent porosity ceramics were fabricated from fly ash cenosphere. Effects of sintering temperature and CaCO3 on the apparent porosity were investigated. More importantly, the formation mechanism of high apparent porosity was proposed. Results showed that the sintering temperature decreased the apparent porosity in densification process. The addition of CaCO3 improved the apparent porosity in two ways: one was that CO2 emission from CaCO3 decomposition promoted the formation of pores in ceramics; the other one was that CaO from decomposed CaCO3 was transformed into anorthite with fly ash cenosphere, which generated the porous structure of fly ash cenosphere shell. In this work, the apparent porosity of ceramics with 30 wt% CaCO3 sintered at 1250 °C reached 59.25%, and the corresponding compressive strength was 70 ± 2.58 MPa. Results also indicated that the skeleton structure of interconnected fly ash cenosphere guaranteed a relatively high mechanical strength of this porous ceramics.

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粉煤灰空心球制备高表观孔隙率陶瓷的形成机理
多孔陶瓷具有较高的表观孔隙率,在各个领域有着广泛的应用。本文以粉煤灰空心球为原料制备了高表观孔隙率陶瓷。研究了烧结温度和碳酸钙对表观孔隙率的影响。更重要的是,提出了高表观孔隙度的形成机理。结果表明,烧结温度降低了致密化过程中的表观孔隙率。CaCO3的加入从两个方面改善了表观孔隙率:一是CaCO3分解释放的CO2促进了陶瓷孔隙的形成;二是分解后的CaCO3中的CaO与粉煤灰空心球一起转化为钙长石,形成粉煤灰空心球壳的多孔结构。在1250 ℃下烧结,CaCO3质量分数为30 wt%的陶瓷表观孔隙率达到59.25%,抗压强度为70 ± 2.58 MPa。结果还表明,互连粉煤灰空心球的骨架结构保证了该多孔陶瓷具有较高的机械强度。
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来源期刊
Journal of Alloys and Compounds
Journal of Alloys and Compounds 工程技术-材料科学:综合
CiteScore
11.10
自引率
14.50%
发文量
5146
审稿时长
67 days
期刊介绍: The Journal of Alloys and Compounds is intended to serve as an international medium for the publication of work on solid materials comprising compounds as well as alloys. Its great strength lies in the diversity of discipline which it encompasses, drawing together results from materials science, solid-state chemistry and physics.
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