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Structural studies of thallium containing germanate and borate glasses and crystalline phases
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Laorodphan, Nattapol (2012) Structural studies of thallium containing germanate and borate glasses and crystalline phases. PhD thesis, University of Warwick.
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Official URL: http://webcat.warwick.ac.uk/record=b2685731~S1
Abstract
The structure of glasses and devitrified phases, in Tl2O⋅GeO2 and Tl2O⋅B2O3 systems, have been
investigated using solid-state nuclear magnetic resonance (NMR), neutron diffraction and
Raman spectroscopy. Gas pycnometry, thermal analysis and powder X-ray diffraction (XRD)
have also been used to characterise and measure properties of glasses and devitrified phases.
The crystallisation study showed that metastable crystalline phases were obtained from lowtemperature
heat-treatment. X-ray diffraction of devitrification products, obtained at higher
temperature, indicates crystallisation of the corresponding, more stable, stoichiometric
compounds from the glass but with one or more second phases. Thallium NMR studies reveal
that various chemical environments of thallium are present in the heat-treated samples. For the
Tl2Ge4O9 sample, whose crystal structure is known, magic angle spinning NMR reveals the
presence of one thallium site, the [Ge3O9] ring structure was observed using Raman
spectroscopy.
A germanate anomaly is present in the thallium germanate glasses indicated by a minimum
value of molar volume at x ~ 0.15. Neutron diffraction and Raman spectroscopy confirm the
change in the coordination number of germanium from [GeO4] to [GeO6 or 5]. Tl solid-state
NMR suggests that at least two thallium sites are also present in the glass, low and high
coordinated thallium. Tl-NMR spectra are broad and shifted mainly due to the chemical shift
dispersion and chemical shift anisotropy interaction, respectively. T2 measurements confirmed
that dipole-dipole and pseudodipole or exchange interactions are stronger in high thallium
content glasses. A 203Tl enrichment study determined that the broadening due to the exchange
interaction is ~ 10 kHz.
Only three crystalline thallium borate phases were obtained, either singly or in combination
with each other. Density data, X-ray diffraction patterns and solid-state NMR results of the
three phases formed support what structural information exists in the literature. Chemical shift
interaction and chemical shift dispersion contribute to the line broadening and lineshape of Tl
NMR of TlB5O8 and TlB3O5 containing sample. Dipolar interaction and the Tl…Tl exchange
interaction are stronger in the Tl2B4O7 sample. The chemical shift anisotropy parameters of
TlB5O8 and TlB3O5 are presented.
A borate anomaly is present in thallium borate glasses with a minimum value of molar volume
at x ~ 0.28. Neutron diffraction and solid-state NMR spectroscopy confirm the change in the
coordination number of boron to oxygen atoms from [BO3] to [BO4]. N4 values obtained from
both techniques are very close and are larger than found for alkali borate glasses. Raman
spectroscopy also reveals the changes in boron-oxygen superstructural units. 205Tl solid-state
NMR suggests that at least two thallium sites are present in the glass, low and high coordinated
thallium. Tl-NMR spectra are broad and shifted mainly due to the chemical shift dispersion and
chemical shift anisotropy interaction, respectively. T2 measurement confirmed that
dipole-dipole and exchange interactions occur in glasses throughout the range of studied
compositions.
Item Type: | Thesis (PhD) | ||||
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Subjects: | Q Science > QD Chemistry | ||||
Library of Congress Subject Headings (LCSH): | Thallium -- Structure, Thallium -- Spectra, Glass, Borates, Germanium compounds, Nuclear magnetic resonance | ||||
Official Date: | September 2012 | ||||
Dates: |
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Institution: | University of Warwick | ||||
Theses Department: | Department of Physics | ||||
Thesis Type: | PhD | ||||
Publication Status: | Unpublished | ||||
Supervisor(s)/Advisor: | Holland, Diane | ||||
Sponsors: | Thailand; Institute of Physics (Great Britain) | ||||
Extent: | xv, 160 leaves : illustrations. | ||||
Language: | eng |
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