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Coordination of Boron in Nominally Boron-Free Rock Forming Silicates: Evidence for Incorporation of BO3 groups in Clinopyroxene

Hålenius, Ulf (author)
Naturhistoriska riksmuseet,Enheten för geovetenskap
Edén, Mattias (author)
Stockholms universitet,Avdelningen för fysikalisk kemi,Mattias Edén,Stockholm universitet
Skogby, Henrik (author)
Naturhistoriska riksmuseet,Enheten för geovetenskap
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Nazzareni, Sabrina (author)
Università di Perugia
Kristiansson, Per (author)
Lund University,Lunds universitet,Kärnfysik,Fysiska institutionen,Institutioner vid LTH,Lunds Tekniska Högskola,Nuclear physics,Department of Physics,Departments at LTH,Faculty of Engineering, LTH
Resmark, Jeppa (author)
Lunds universitet
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 (creator_code:org_t)
Elsevier BV, 2010
2010
English.
In: Geochimica et Cosmochimica Acta. - : Elsevier BV. - 0016-7037 .- 1872-9533. ; 74, s. 5672-5679
  • Journal article (peer-reviewed)
Abstract Subject headings
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  • To explore mechanisms of B-incorporation in common chain silicates we have investigated synthetic diopside samples produced under boron-saturated conditions by 11B and 29Si magic-angle spinning (MAS) NMR and single-crystal NRA, FTIR, EMP and XRD/SREF techniques. Our samples contain 0.14–0.65 wt.% B2O3. NMR reveals that B is predominantly present in trigonal coordination in the clinopyroxene structure. This observation is supported by vibrational bands characteristic for B–O stretching in BO3 groups in the range 1250–1400 cm−1 in polarised single crystal FTIR-spectra. Single crystal structure refinements suggest that boron replaces Si at the T site. Combined, these results suggest that boron replacement for Si at the T-site leads to disruption of one of the T–O bonds of the nominal clinopyroxene structure resulting in replacement of SiO4 tetrahedra by BO3 groups. Our results show that high concentrations of boron can be incorporated in the nominally boron-free diopside. Elevated B-concentrations in the present calcic clinopyroxenes are accompanied by modifications of the diopside crystal structure involving the breaking of one T–O bond and simultaneous formation of vacancies at the octahedral M2 site. These structural modifications destabilize the structure and constitute thereby limiting factors for incorporating higher boron concentrations in diopside.    

Subject headings

NATURVETENSKAP  -- Kemi -- Oorganisk kemi (hsv//swe)
NATURAL SCIENCES  -- Chemical Sciences -- Inorganic Chemistry (hsv//eng)
NATURVETENSKAP  -- Fysik -- Subatomär fysik (hsv//swe)
NATURAL SCIENCES  -- Physical Sciences -- Subatomic Physics (hsv//eng)
NATURVETENSKAP  -- Geovetenskap och miljövetenskap -- Geokemi (hsv//swe)
NATURAL SCIENCES  -- Earth and Related Environmental Sciences -- Geochemistry (hsv//eng)

Keyword

Inorganic chemistry
Oorganisk kemi
The changing Earth

Publication and Content Type

ref (subject category)
art (subject category)

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