NOx degradation by photocatalytic mortars: The underlying role of the CH and C-S-H carbonation

被引:47
作者
Kaja, A. M. [1 ]
Brouwers, H. J. H. [1 ]
Yu, Q. L. [1 ]
机构
[1] Eindhoven Univ Technol, Dept Built Environm, NL-5600 MB Eindhoven, Netherlands
关键词
Photocatalytic mortar; Nitrogen oxides; Carbonation; Pore structure; Selectivity; CEMENT PASTE; ACCELERATED CARBONATION; MICROSTRUCTURE; CONCRETE; ABATEMENT; TITANIA; WATER; OXIDE; DECALCIFICATION; EFFICIENCIES;
D O I
10.1016/j.cemconres.2019.105805
中图分类号
TU [建筑科学];
学科分类号
0813 ;
摘要
This study aims to understand the impact of carbonation mechanism of C-S-H and CH in photocatalytic mortars on NOx removal efficiency. Changes in surface chemistry and microstructure induced by the carbonation of portlandite and C-S-H (AFm/AFt) were correlated with the photocatalytic efficiency of the mortars doped with three types of titania-based photocatalysts. Furthermore, the influence of cementitious matrix on the photo-catalytic selectivity was evaluated by studying the capacity of hydration/carbonation products to adsorb NO2. The study revealed that in terms of both photocatalytic efficiency and selectivity, mortars with microsilica addition exhibit superior properties over the pure cement-based mortars upon carbonation. Carbonation of C-S-H (AFm/AFt) gel results in the formation of capillary pores between10-50 nm, which outbalances the shielding effects of carbonates formed, leading to the enhanced photocatalytic properties. Moreover, C-S-H gel maintains its high NO2 adsorption capacity even after carbonation, resulting in the high selectivity of the photocatalysis.
引用
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页数:11
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