Effect of Ti on crystal transition and solid solution characteristics of white Portland cement clinker
Source abstract
Abstract
Titanium (Ti) is a common trace element in white Portland cement clinker. Ti4+ generally replaces Si4+ to form a solid solution in silicate minerals, which has an important influence on the mineral crystal form of white cement clinker. In this paper, the effects of Ti on the mineral composition and solid solution characteristics of white Portland cement clinker were studied by X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), scanning electron microscopy–energy dispersive X-ray spectroscopy (SEM-EDS) and Rietveld quantitative analysis. The results showed that the incorporation of titanium dioxide (TiO2) stabilised the highly active α′H-belite (C2S), but over 1% will form calcium titanate (CaTiO3) The crystal form of alite (C3S) was T3→M1→M3→R with the increase of titanium dioxide content. Ti elements tended first to be solid soluble in the intermediate phase, then C2S, and finally C3S. The content of Ti in α′H-C2S was higher than that in β-C2S. With the increase of titanium dioxide content, the calcium–silicon ratio of C2S decreased first and then increased. In silicate minerals, Ti4+ replaced Si4+ to form titanate [TiO4]. The Ca2+ ion in α′H-C2S was placed in a more electronegative environment, resulting in a larger binding energy of electrons in the 2p orbit.
Source: crossref · Quality: baseline
Research context
OpenAlex topics: Concrete and Cement Materials Research · Rock Mechanics and Modeling · Drilling and Well Engineering
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
School of Materials Science and Engineering, Nanchang University, Nanchang Jiangxi, P. R. China
School of Materials Science and Engineering, Nanchang University, Nanchang Jiangxi, P. R. China (corresponding author: )
References (24)
Show source-provided references
1. 10.1016/j.mseb.2017.12.02010.1016/j.mseb.2017.12.020 ↗
2. 10.1154/1.152307910.1154/1.1523079 ↗
3. 10.1107/S002188980100248510.1107/S0021889801002485 ↗
4. 10.1016/j.cemconres.2004.12.00310.1016/j.cemconres.2004.12.003 ↗
5. 10.1111/j.1151-2916.1995.tb07982.x10.1111/j.1151-2916.1995.tb07982.x ↗
6. 10.1016/j.cemconcomp.2012.12.00310.1016/j.cemconcomp.2012.12.003 ↗
7. 10.1016/j.cemconres.2003.10.02010.1016/j.cemconres.2003.10.020 ↗
8. Li J · ACS Sustainable Chemistry & Engineering · 2018 · 7 · 231610.1021/acssuschemeng.8b05060 ↗
9. Liu X · Physics and Chemistry of Minerals · 1993 · 20 · 171
10. 10.1007/s11595-009-5830-x10.1007/s11595-009-5830-x ↗
11. 10.1016/0008-8846(82)90103-X10.1016/0008-8846(82)90103-X ↗
12. 10.1016/0008-8846(84)90054-110.1016/0008-8846(84)90054-1 ↗
13. 10.1107/S002188989800985610.1107/S0021889898009856 ↗
14. 10.1016/j.ceramint.2009.02.00610.1016/j.ceramint.2009.02.006 ↗
15. 10.1016/j.conbuildmat.2019.05.04510.1016/j.conbuildmat.2019.05.045 ↗
16. 10.2138/am-1999-11-120410.2138/am-1999-11-1204 ↗
17. 10.1107/S002188986900655810.1107/S0021889869006558 ↗
18. 10.1063/1.35146510.1063/1.351465 ↗
19. 10.1016/j.cemconres.2016.09.01210.1016/j.cemconres.2016.09.012 ↗
20. 10.1016/j.conbuildmat.2017.03.12910.1016/j.conbuildmat.2017.03.129 ↗
21. 10.1016/j.jclepro.2015.09.12710.1016/j.jclepro.2015.09.127 ↗
22. Wumme WG · Neues Jahrbuch für Mineralogie Abhandlungen · 1995 · 169 · 35
23. 10.1016/j.carbon.2008.09.04510.1016/j.carbon.2008.09.045 ↗
24. 10.1016/j.cemconres.2018.10.01910.1016/j.cemconres.2018.10.019 ↗