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Amino-Alkylphosphonate-Grafted TiO(2): How the Alkyl Chain Length Impacts the Surface Properties and the Adsorption Efficiency for Pd
[Image: see text] Amino-alkylphosphonic acid-grafted TiO(2) materials are of increasing interest in a variety of applications such as metal sorption, heterogeneous catalysis, CO(2) capture, and enzyme immobilization. To date, systematic insights into the synthesis–properties–performance correlation...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2022
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9753204/ https://www.ncbi.nlm.nih.gov/pubmed/36530305 http://dx.doi.org/10.1021/acsomega.2c06020 |
Sumario: | [Image: see text] Amino-alkylphosphonic acid-grafted TiO(2) materials are of increasing interest in a variety of applications such as metal sorption, heterogeneous catalysis, CO(2) capture, and enzyme immobilization. To date, systematic insights into the synthesis–properties–performance correlation are missing for such materials, albeit giving important know-how towards their applicability and limitations. In this work, the impact of the chain length and modification conditions (concentration and temperature) of amino-alkylphosphonic acid-grafted TiO(2) on the surface properties and adsorption performance of palladium is studied. Via grafting with aminomethyl-, 3-aminopropyl-, and 6-aminohexylphosphonic acid, combined with the spectroscopic techniques (DRIFT, (31)P NMR, XPS) and zeta potential measurements, differences in surface properties between the C1, C3, and C6 chains are revealed. The modification degree decreases with increasing chain length under the same synthesis conditions, indicative of folded grafted groups that sterically shield an increasing area of binding sites with increasing chain length. Next, all techniques confirm the different surface interactions of a C1 chain compared to a C3 or C6 chain. This is in line with palladium adsorption experiments, where only for a C1 chain, the adsorption efficiency is affected by the precursor concentration used for modification. The absence of a straightforward correlation between the number of free NH(2) groups and the adsorption capacity for the different chain lengths indicates that other chain-length-specific surface interactions are controlling the adsorption performance. The increasing pH stability in the order of C1 < C3 < C6 can possibly be associated to a higher fraction of inaccessible hydrophilic sites due to the presence of folded structures. Lastly, the comparison of adsorption performance and pH stability with 3-aminopropyl(triethoxysilane)-grafted TiO(2) reveals the applicability of both grafting methods depending on the envisaged pH during sorption. |
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