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Zirconium Containing Periodic Mesoporous Organosilica: The Effect of Zr on CO2 Sorption at Ambient Conditions

期刊

JOURNAL OF COMPOSITES SCIENCE
卷 6, 期 6, 页码 -

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MDPI
DOI: 10.3390/jcs6060168

关键词

CO2 uptake; physisorption; periodic mesoporous organosilica; zirconia; one pot synthesis

资金

  1. Ohio Research Scholars Program Research Cluster on Surfaces in Advanced Materials

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Two series of Zr-PMO materials were synthesized using different precursors, and their structural and surface properties were tailored by controlling the synthesis parameters. The Zr-PMOs showed high CO2 uptake, indicating their potential in capturing CO2 at ambient conditions.
Two series of zirconium-incorporated-periodic-mesoporous-organosilica (Zr-PMO) materials were successfully prepared, via a co-condensation strategy, in the presence of Pluronic P123 triblock copolymer. The first series of Zr-PMO was prepared using tris[3-(trimethoxysilyl)propyl]isocyanurate (ICS), tetraethylorthosilicate (TEOS), and zirconyl chloride octahydrate(ZrCO), denoted as Zr-I-PMO, where I refers to ICS. The second series was synthesized using bis(triethoxysilyl)benzene (BTEE), TEOS, and ZrCO as precursors, named as Zr-B-PMO, where B refers to BTEE. Zr-PMO samples exhibit type (IV) adsorption isotherms, with a distinct H2-hysteresis loop and well-developed structural parameters, such as pore volume, pore width, high surface area, and narrow pore-size distribution. Structural properties were studied by varying the Zr:Si ratio, adding TEOS at different time intervals, and changing the amount of block copolymer-Pluronic P123 used as well as the calcination temperature. Surface characteristics were tailored by precisely controlling the Zr:Si ratio, upon varying the amount of TEOS present in the mesostructures. The addition of TEOS at different synthesis stages, notably, enhanced the pore size and surface area of the resulting Zr-I-PMO samples more than the Zr-B-PMO samples. Changing the amount of block copolymer, also, played a significant role in altering the textural and morphological properties of the Zr-I-PMO and Zr-B-PMO samples. Optimizing the amount of Pluronic P123 added is crucial for tailoring the surface properties of Zr-PMOs. The prepared Zr-PMO samples were examined for use in CO2 sorption, at ambient temperature and pressure (25 degrees C, 1.2 bar pressure). Zr-PMO samples displayed a maximum CO2 uptake of 2.08 mmol/g, at 25 degrees C and 1.2 bar pressure. However, analogous zirconium samples, without any bridging groups, exhibited a significantly lower CO2 uptake, of 0.72 mmol/g, under the same conditions. The presence of isocyanurate- and benzene-bridging groups in Zr-I-PMO and Zr-B-PMO samples enhances the CO2 sorption. Interestingly, results illustrate that Zr-PMO materials show potential in capturing CO2, at ambient conditions.

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