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Title: Hybrid inorganic-organic adsorbents, Part 1: synthesis and characterization of mesoporous zirconium titanate frameworks containing coordinating organic functionalities.
Authors: Griffith, CS
Reyes, MDL
Scales, N
Hanna, JV
Luca, V
Keywords: Zirconium
Adsorbents
Hybridization
Nuclear Magnetic Resonance
Organic Acids
Isotopes
Issue Date: 22-Dec-2010
Publisher: American Chemical Society
Citation: Griffith, C. S., Reyes, M. D. L., Scales, N., Hanna, J. V., & Luca, V. (2010). Hybrid inorganic−organic adsorbents, Part 1: synthesis and characterization of mesoporous zirconium titanate frameworks containing coordinating organic functionalities. ACS Applied Materials & Interfaces, 2(12), 3436-3446.
Abstract: A series of functional hybrid inorganic−organic adsorbent materials have been prepared through postsynthetic grafting of mesoporous zirconium titanate xerogel powders using a range of synthesized and commercial mono-, bis-, and tris-phosphonic acids, many of which have never before been investigated for the preparation of hybrid phases. The hybrid materials have been characterized using thermogravimetric analysis, diffuse reflectance infrared (DRIFT) and 31P MAS NMR spectroscopic techniques and their adsorption properties studied using a 153Gd radiotracer. The highest level of surface functionalization (molecules/nm2) was observed for methylphosphonic acid (3 molecules/nm2). The level of functionalization decreased with an increase in the number of potential surface coordinating groups of the phosphonic acids. Spectral decomposition of the DRIFT and 31P MAS NMR spectra showed that each of the phosphonic acid molecules coordinated strongly to the metal oxide surface but that for the 1,1-bis-phosphonic acids and tris-phosphonic acids the coordination was highly variable resulting in a proportion of free or loosely coordinated phosphonic acid groups. Functionalization of a porous mixed metal oxide framework with the tris-methylenephosphonic acid (ATMP-ZrTi-0.33) resulted in a hybrid with the highest affinity for 153Gd3+ in nitric acid solutions across a wide range of acid concentrations. The ATMP-ZrTi-0.33 hybrid material extracted 153Gd3+ with a Kd value of 1 × 104 in 0.01 M HNO3 far exceeding that of the other hybrid phases. The unfunctionalized mesoporous mixed metal oxide had negligible affinity for Gd3+ (Kd < 100) under identical experimental conditions. It has been shown that the presence of free or loosely coordinated phosphonic acid groups does not necessarily translate to affinity for 153Gd3+. The theoretical cation exchange capacity of the ATMP-ZrTi-0.33 hybrid phase for Gd3+ has been determined to be about 0.005 mmol/g in 0.01 M HNO3. This behavior and that of the other hybrid phases suggests that the surface-bound ATMP ligand functions as a chelating ligand toward 153Gd3+ under these acidic conditions. © 2010, American Chemical Society
URI: http://dx.doi.org/10.1021/am100891u
http://apo.ansto.gov.au/dspace/handle/10238/2934
ISSN: 1944-8244
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