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Surface protolytic property characterization of hydroxyapatite and titanium dioxide nanoparticles

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    0506352 - ÚMCH 2020 RIV GB eng J - Journal Article
    Kukleva, E. - Suchánková, P. - Štamberg, K. - Vlk, M. - Šlouf, Miroslav - Kozempel, J.
    Surface protolytic property characterization of hydroxyapatite and titanium dioxide nanoparticles.
    RSC Advances. Roč. 9, č. 38 (2019), s. 21989-21995. E-ISSN 2046-2069
    R&D Projects: GA ČR(CZ) GA17-05007S; GA MŠMT(CZ) LO1507; GA MZd(CZ) NV16-30544A
    Institutional support: RVO:61389013
    Keywords : hydroxyapatite and titanium dioxide nanoparticles * modelling of the sorption mechanism
    OECD category: Polymer science
    Impact factor: 3.119, year: 2019
    Method of publishing: Open access
    https://pubs.rsc.org/en/content/articlepdf/2019/ra/c9ra03698a

    We provide characterization data of hydroxyapatite (nHAp) and titanium dioxide (nTiO2) nanoparticles as potential materials for ion sorption, e.g. in targeted therapy, barrier materials for waste repositories or photovoltaics. The study is focused on the determination of the values of protonation and ion exchange constants and site densities (∑SOH, ∑X [mol kg−1]) of nTiO2 and nHAp for further Ra kinetics and sorption experiments. These data are very important for further investigation of the materials, which can be used e.g. as drug delivery systems or in engineered barriers of deep geological repositories. The characterization was based on the evaluation of the dependence of titrating agent consumption on pH. Titration results were evaluated on the basis of several model combinations, however the combination of the Chemical Equilibrium Model (CEM) and Ion Exchange Model (IExM) fits best to the experimental titration curves. However, the differences between the two sorbents were relatively large. Due to stability in a broad pH range and available surface sites, nTiO2 seems to have a wide application range. The applicability of nHAp is not so wide because of its dissolution under pH 5. Both sorbents are virtually able to sorb cationic species on deprotonated edge and layer sites with different capacities, which can be important for sorption and decontaminating applications.
    Permanent Link: http://hdl.handle.net/11104/0298196

     
     
Number of the records: 1  

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