Bifluoride ([HF2]−) formation at the fluoridated aluminium hydroxide/water interface. Issue 22 (25th February 2016)
- Record Type:
- Journal Article
- Title:
- Bifluoride ([HF2]−) formation at the fluoridated aluminium hydroxide/water interface. Issue 22 (25th February 2016)
- Main Title:
- Bifluoride ([HF2]−) formation at the fluoridated aluminium hydroxide/water interface
- Authors:
- Shimizu, Kenichi
Driver, Gordon W.
Lucas, Marie
Sparrman, Tobias
Shchukarev, Andrey
Boily, Jean-François - Abstract:
- Abstract : Bifluoride-type species are formed at fluoride-exchanged aluminium hydroxide surfaces contacted with aqueous solutions. First layer surface species are anchors for growth of multi-layered species towards the solution. Abstract : This study uncovers bifluoride-type (difluorohydrogenate(i ); [HF2 ] − ) species formed at mineral/water interfaces. Bifluoride forms at Al–F surface sites resulting from the partial fluoridation of gibbsite (γ-Al(OH3 )) and bayerite (α-Al(OH3 )) particles exposed to aqueous solutions of 50 mM NaF. Fluoride removal from these solutions is proton-promoted and results in a strongly self-buffered suspensions at circumneutral pH, proceeds at a F : H consumption ratio of 2 : 1, and with recorded losses of up to 17 mM fluoride (58 F nm −2 ). These loadings exceed crystallographic site densities by a factor of 3–4, yet the reactions have no resolvable impact on particle size, shape and mineralogy. X-ray photoelectron spectroscopy (XPS) of frozen (−155 °C) wet mineral pastes revealed coexisting surface F − and HF 0 species. Electron energy loss features pointed to multilayer distribution of these species at the mineral/water interface. XPS also uncovered a distinct form of Na + involved in binding fluoride-bearing species. XPS and solid state magic angle spinning 19 F nuclear magnetic resonance measurements showed that these fluoride species were highly comparable to a sodium-bifluoride (NaHF2 ) reference. First layer surface species areAbstract : Bifluoride-type species are formed at fluoride-exchanged aluminium hydroxide surfaces contacted with aqueous solutions. First layer surface species are anchors for growth of multi-layered species towards the solution. Abstract : This study uncovers bifluoride-type (difluorohydrogenate(i ); [HF2 ] − ) species formed at mineral/water interfaces. Bifluoride forms at Al–F surface sites resulting from the partial fluoridation of gibbsite (γ-Al(OH3 )) and bayerite (α-Al(OH3 )) particles exposed to aqueous solutions of 50 mM NaF. Fluoride removal from these solutions is proton-promoted and results in a strongly self-buffered suspensions at circumneutral pH, proceeds at a F : H consumption ratio of 2 : 1, and with recorded losses of up to 17 mM fluoride (58 F nm −2 ). These loadings exceed crystallographic site densities by a factor of 3–4, yet the reactions have no resolvable impact on particle size, shape and mineralogy. X-ray photoelectron spectroscopy (XPS) of frozen (−155 °C) wet mineral pastes revealed coexisting surface F − and HF 0 species. Electron energy loss features pointed to multilayer distribution of these species at the mineral/water interface. XPS also uncovered a distinct form of Na + involved in binding fluoride-bearing species. XPS and solid state magic angle spinning 19 F nuclear magnetic resonance measurements showed that these fluoride species were highly comparable to a sodium-bifluoride (NaHF2 ) reference. First layer surface species are represented as Al–F–H–F–Al and Al–F–Na–F–Al, and may form multi-layered species into the mineral/water interface. These results consequently point to a potentially overlooked inorganic fluorine species in a technologically relevant mineral/water interfacial systems. … (more)
- Is Part Of:
- Dalton transactions. Volume 45:Issue 22(2016)
- Journal:
- Dalton transactions
- Issue:
- Volume 45:Issue 22(2016)
- Issue Display:
- Volume 45, Issue 22 (2016)
- Year:
- 2016
- Volume:
- 45
- Issue:
- 22
- Issue Sort Value:
- 2016-0045-0022-0000
- Page Start:
- 9045
- Page End:
- 9050
- Publication Date:
- 2016-02-25
- Subjects:
- Chemistry, Inorganic -- Periodicals
Chemistry, Physical and theoretical -- Periodicals
Chemistry, Inorganic -- Periodicals
546.05 - Journal URLs:
- http://pubs.rsc.org/en/journals/journalissues/dt#!issueid=dt043040&type=current&issnprint=1477-9226 ↗
http://www.rsc.org/ ↗ - DOI:
- 10.1039/c5dt04425a ↗
- Languages:
- English
- ISSNs:
- 1477-9226
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 3517.830000
British Library DSC - BLDSS-3PM
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- 250.xml