Ti K-edge XANES (X-ray absorption near edge structure) spectroscopy has been used to study the local coordination of titanium in biocompatible and bioresorbable TiO2-CaO-Na2O-P2O5 glasses. Both conventional melt-quenched glasses of composition (TiO2)x(CaO)0.30(Na2O)0.20-x(P2O5)0.50, where x = 0.01, 0.03 and 0.05, and sol-gel derived (TiO2)0.25(CaO)0.25(P2O5)0.50 glass have been studied. The results show that in all the materials studied, titanium is surrounded by an octahedron of oxygen atoms. Further analysis reveals that the TiO6 site in the amorphous samples is not heavily distorted relative to that in rutile, anatase or CaSiTiO5. The spectra from the (TiO2)0.25(CaO)0.25(P2O5)0.50 sol-gel samples reveal greater distortion in the TiO6 site in the dried gel compared to the heat-treated sol-gel glass. The XANES spectra from melt-quenched glass samples soaked in distilled water for various times do not shown any evidence of degradation of the titanium site over periods of up to 14 days.

Download full-text PDF

Source
http://dx.doi.org/10.1007/s10856-007-3342-9DOI Listing

Publication Analysis

Top Keywords

k-edge xanes
8
study local
8
bioresorbable tio2-cao-na2o-p2o5
8
tio2-cao-na2o-p2o5 glasses
8
tio6 site
8
xanes study
4
local environment
4
titanium
4
environment titanium
4
titanium bioresorbable
4

Similar Publications

Elucidation of the Off-Center Displaced Mo in Octahedral Coordination in BaMoO.

Inorg Chem

January 2025

Radiation Science & Technology Department, Faculty of Applied Sciences, Delft University of Technology, Mekelweg 15, Delft 2629JB, The Netherlands.

The detailed crystal structure as well as the heat capacity at low temperature and standard entropy of BaMoO are reported for the first time. High-resolution X-ray and neutron diffraction were employed to reveal the structural features of this compound. BaMoO has a six-coordinated Mo and a strongly negative excess volume with respect to the binary oxides.

View Article and Find Full Text PDF

Effects of dimethylarsenate coprecipitation with ferrihydrite on Fe(II)-induced mineral transformation and the release of dimethylarsenate.

Environ Pollut

December 2024

Key Laboratory of Arable Land Conservation (Middle and Lower Reaches of Yangtse River), Ministry of Agriculture and Rural Affairs, College of Resources and Environment, Huazhong Agricultural University, Wuhan, 430070, China; Hubei Key Laboratory of Soil Environment and Pollution Remediation, College of Resources and Environment, Wuhan, 430070, China. Electronic address:

Organoarsenicals are toxic pollutants of global concern, and their environmental geochemical behavior might be greatly controlled by iron (Fe) (hydr)oxides through coprecipitation, which is rarely investigated. Here, the effects of the incorporation of dimethylarsenate (DMAs(V)), a typical organoarsenical, into the ferrihydrite (Fh) structure on the mineral physicochemical properties and Fe(II)-induced phase transformation of DMAs(V)-Fh coprecipitates with As/Fe molar ratios up to 0.0876 ± 0.

View Article and Find Full Text PDF

Nickel and nitrogen co-doped carbon (Ni-N-C) catalysts are attracting attention due to their exceptionally high performance in the electrocatalytic reduction of CO_{2}(CO_{2}RR) to CO. However, the direct experimental insight into the working mechanism of these catalysts is missing, hindering our fundamental understanding and their further improvement. This work sheds light on the nature of adsorbates forming under CO_{2}RR at singly dispersed Ni sites.

View Article and Find Full Text PDF

We analyze the structures of the low-spin (LS) ground state and the high-spin (HS) lowest excited state of the iron-(II)-tris bipyridine complex ([Fe(bpy)]) using density functional theory PBE methods, modeling the solvent interactions with conductor-like polarizable continuum model. These calculations are globally benchmarked against a wide range of experimental observables that include ultraviolet-visible linear absorption and circular dichroism (CD) spectra and Fe K-edge x-ray absorption near edge spectra (XANES). The calculations confirm the already established D geometry of the LS state, as well as a departure from this geometry for the HS state, with the appearance of inequivalent Fe-N bond elongations.

View Article and Find Full Text PDF

Formation and Segregation of the Ru- and Rh-MgO Solid Solutions.

ACS Omega

November 2024

Department of Applied Chemistry, School of Advanced Engineering, Kogakuin University, 2665-1 Nakano-machi Hachioji-city, 192-0015 Tokyo, Japan.

Structural changes in Ru- and Rh-loaded magnesium oxide (MgO) subjected to thermal treatment were investigated by using X-ray absorption spectroscopy. The thermal treatment of the MgO-loaded Ru and Rh nanoparticles led to the formation of Ru-MgO and Rh-MgO solid solutions, respectively. The valences of Ru and Rh in the solutions were 4+ and 3+, respectively, as determined by the Ru and Rh K-edge X-ray absorption near-edge structure (XANES).

View Article and Find Full Text PDF

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!