Optical absorption, Mössbauer, and FTIR spectroscopic studies of two blue bazzites

Two samples of bazzite, a very rare Sc analog of beryl, from Tørdal, Telemark, Norway and Kent, Central Kazakhstan were studied by electron microprobe, optical absorption, and Mössbauer spectroscopies; the latter sample was also studied by FTIR. Electron microprobe results show that the Norway bazzi...

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Veröffentlicht in:Physics and chemistry of minerals 2017-07, Vol.44 (7), p.497-507
Hauptverfasser: Taran, Michail N., Dyar, M. Darby, Khomenko, Vladimir M., Boesenberg, Joseph S.
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description Two samples of bazzite, a very rare Sc analog of beryl, from Tørdal, Telemark, Norway and Kent, Central Kazakhstan were studied by electron microprobe, optical absorption, and Mössbauer spectroscopies; the latter sample was also studied by FTIR. Electron microprobe results show that the Norway bazzite is composed of two bazzites with slightly different FeO contents, viz. 5.66 and 5.43 wt%. The Kazakhstan sample consists of several varieties of bazzite displaying strong differences in iron, manganese, magnesium, and aluminum contents (in wt%): FeO from 2.02 to 6.73, MnO from 0.89 to 2.98, MgO from 0.37 to 1.86, and Al 2 O 3 from 0.30 to 1.30. Mössbauer spectroscopy shows different degrees of iron oxidation. The Norway bazzite is completely Fe 2+ , while the Kazakhstan sample contains roughly equivalent Fe 3+ and Fe 2+ accommodated in the octahedral site. The difference in iron oxidation causes strong variations in the intensity of the broad optical absorption band around 13,850 cm −1 , which is assigned to Fe 2+ → Fe 3+ IVCT; as a result, there are strong differences in the intensity of blue color. Dichroism ( E || c  ≫  E ⊥ c ) is much stronger in the Kazakhstan sample than in the Norway one. Intensities of the electronic spin-allowed bands of [6] Fe 2+ at ~8900 and ~10,400 cm −1 are somewhat higher in the latter than in the former. FTIR spectra of the sample from Kent show the presence of only water type II molecules with the H–H vector perpendicular to the c -axis, in contrast to more typical beryls that always show at least weak minor bands of H 2 O I. This result shows that trapped water molecules in structural channels of studied bazzite occupy only sites next to or between six-membered rings centered by Na atoms. Definite structure can be observed in the vicinities of ν 2 and ν 3 peaks. Peaks at 1621 and 3663 cm −1 are assigned to “doubly coordinated” H 2 O (IId), whereas maximums at 1633 and 3643 cm −1 likely represent “singly coordinated” H 2 O (IIs). Interpretation of the third components in complex ν 2 and ν 3 bands needs further investigations.
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Darby ; Khomenko, Vladimir M. ; Boesenberg, Joseph S.</creator><creatorcontrib>Taran, Michail N. ; Dyar, M. Darby ; Khomenko, Vladimir M. ; Boesenberg, Joseph S.</creatorcontrib><description>Two samples of bazzite, a very rare Sc analog of beryl, from Tørdal, Telemark, Norway and Kent, Central Kazakhstan were studied by electron microprobe, optical absorption, and Mössbauer spectroscopies; the latter sample was also studied by FTIR. Electron microprobe results show that the Norway bazzite is composed of two bazzites with slightly different FeO contents, viz. 5.66 and 5.43 wt%. The Kazakhstan sample consists of several varieties of bazzite displaying strong differences in iron, manganese, magnesium, and aluminum contents (in wt%): FeO from 2.02 to 6.73, MnO from 0.89 to 2.98, MgO from 0.37 to 1.86, and Al 2 O 3 from 0.30 to 1.30. Mössbauer spectroscopy shows different degrees of iron oxidation. The Norway bazzite is completely Fe 2+ , while the Kazakhstan sample contains roughly equivalent Fe 3+ and Fe 2+ accommodated in the octahedral site. The difference in iron oxidation causes strong variations in the intensity of the broad optical absorption band around 13,850 cm −1 , which is assigned to Fe 2+ → Fe 3+ IVCT; as a result, there are strong differences in the intensity of blue color. Dichroism ( E || c  ≫  E ⊥ c ) is much stronger in the Kazakhstan sample than in the Norway one. Intensities of the electronic spin-allowed bands of [6] Fe 2+ at ~8900 and ~10,400 cm −1 are somewhat higher in the latter than in the former. FTIR spectra of the sample from Kent show the presence of only water type II molecules with the H–H vector perpendicular to the c -axis, in contrast to more typical beryls that always show at least weak minor bands of H 2 O I. This result shows that trapped water molecules in structural channels of studied bazzite occupy only sites next to or between six-membered rings centered by Na atoms. Definite structure can be observed in the vicinities of ν 2 and ν 3 peaks. Peaks at 1621 and 3663 cm −1 are assigned to “doubly coordinated” H 2 O (IId), whereas maximums at 1633 and 3643 cm −1 likely represent “singly coordinated” H 2 O (IIs). 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Darby</creatorcontrib><creatorcontrib>Khomenko, Vladimir M.</creatorcontrib><creatorcontrib>Boesenberg, Joseph S.</creatorcontrib><title>Optical absorption, Mössbauer, and FTIR spectroscopic studies of two blue bazzites</title><title>Physics and chemistry of minerals</title><addtitle>Phys Chem Minerals</addtitle><description>Two samples of bazzite, a very rare Sc analog of beryl, from Tørdal, Telemark, Norway and Kent, Central Kazakhstan were studied by electron microprobe, optical absorption, and Mössbauer spectroscopies; the latter sample was also studied by FTIR. Electron microprobe results show that the Norway bazzite is composed of two bazzites with slightly different FeO contents, viz. 5.66 and 5.43 wt%. The Kazakhstan sample consists of several varieties of bazzite displaying strong differences in iron, manganese, magnesium, and aluminum contents (in wt%): FeO from 2.02 to 6.73, MnO from 0.89 to 2.98, MgO from 0.37 to 1.86, and Al 2 O 3 from 0.30 to 1.30. Mössbauer spectroscopy shows different degrees of iron oxidation. The Norway bazzite is completely Fe 2+ , while the Kazakhstan sample contains roughly equivalent Fe 3+ and Fe 2+ accommodated in the octahedral site. The difference in iron oxidation causes strong variations in the intensity of the broad optical absorption band around 13,850 cm −1 , which is assigned to Fe 2+ → Fe 3+ IVCT; as a result, there are strong differences in the intensity of blue color. Dichroism ( E || c  ≫  E ⊥ c ) is much stronger in the Kazakhstan sample than in the Norway one. Intensities of the electronic spin-allowed bands of [6] Fe 2+ at ~8900 and ~10,400 cm −1 are somewhat higher in the latter than in the former. FTIR spectra of the sample from Kent show the presence of only water type II molecules with the H–H vector perpendicular to the c -axis, in contrast to more typical beryls that always show at least weak minor bands of H 2 O I. This result shows that trapped water molecules in structural channels of studied bazzite occupy only sites next to or between six-membered rings centered by Na atoms. Definite structure can be observed in the vicinities of ν 2 and ν 3 peaks. Peaks at 1621 and 3663 cm −1 are assigned to “doubly coordinated” H 2 O (IId), whereas maximums at 1633 and 3643 cm −1 likely represent “singly coordinated” H 2 O (IIs). Interpretation of the third components in complex ν 2 and ν 3 bands needs further investigations.</description><subject>Absorption</subject><subject>Absorption spectra</subject><subject>Aluminum</subject><subject>Aluminum oxide</subject><subject>Atomic structure</subject><subject>Crystallography and Scattering Methods</subject><subject>Dichroism</subject><subject>Earth and Environmental Science</subject><subject>Earth Sciences</subject><subject>Electron probes</subject><subject>Electron spin</subject><subject>Fourier transforms</subject><subject>Geochemistry</subject><subject>Infrared spectroscopy</subject><subject>Iron</subject><subject>Magnesium</subject><subject>Manganese</subject><subject>Mineral Resources</subject><subject>Mineralogy</subject><subject>Mossbauer spectroscopy</subject><subject>Original Paper</subject><subject>Oxidation</subject><subject>Spectrum analysis</subject><subject>Water chemistry</subject><issn>0342-1791</issn><issn>1432-2021</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><sourceid>AFKRA</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><recordid>eNp1kN9KwzAUxoMoOKcP4F3A20VzkrZpLmU4HUwGOq9D0qbSMZuapIh7MF_AFzOjgldenQ_O950_P4QugV4DpeImUMoKSSgIQkshCDtCE8g4I4wyOEYTyjNGQEg4RWchbClNTZFP0PO6j22ld1ib4HzSrpvhx--vEIwerJ9h3dV4sVk-4dDbKnoXKte3FQ5xqFsbsGtw_HDY7AaLjd7v22jDOTpp9C7Yi986RS-Lu838gazW98v57YpozmUklhshq8w2hZFcCmtYnpual41kljdl0pTJChqd2xzqIqupBgZgasu5NrnhU3Q1zu29ex9siGrrBt-llYqxIj3OixKSC0ZXlY4P3jaq9-2b9p8KqDqwUyM7ldipAzvFUoaNmZC83av1f5P_D_0AbYpylA</recordid><startdate>20170701</startdate><enddate>20170701</enddate><creator>Taran, Michail N.</creator><creator>Dyar, M. 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Darby</au><au>Khomenko, Vladimir M.</au><au>Boesenberg, Joseph S.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Optical absorption, Mössbauer, and FTIR spectroscopic studies of two blue bazzites</atitle><jtitle>Physics and chemistry of minerals</jtitle><stitle>Phys Chem Minerals</stitle><date>2017-07-01</date><risdate>2017</risdate><volume>44</volume><issue>7</issue><spage>497</spage><epage>507</epage><pages>497-507</pages><issn>0342-1791</issn><eissn>1432-2021</eissn><abstract>Two samples of bazzite, a very rare Sc analog of beryl, from Tørdal, Telemark, Norway and Kent, Central Kazakhstan were studied by electron microprobe, optical absorption, and Mössbauer spectroscopies; the latter sample was also studied by FTIR. Electron microprobe results show that the Norway bazzite is composed of two bazzites with slightly different FeO contents, viz. 5.66 and 5.43 wt%. The Kazakhstan sample consists of several varieties of bazzite displaying strong differences in iron, manganese, magnesium, and aluminum contents (in wt%): FeO from 2.02 to 6.73, MnO from 0.89 to 2.98, MgO from 0.37 to 1.86, and Al 2 O 3 from 0.30 to 1.30. Mössbauer spectroscopy shows different degrees of iron oxidation. The Norway bazzite is completely Fe 2+ , while the Kazakhstan sample contains roughly equivalent Fe 3+ and Fe 2+ accommodated in the octahedral site. The difference in iron oxidation causes strong variations in the intensity of the broad optical absorption band around 13,850 cm −1 , which is assigned to Fe 2+ → Fe 3+ IVCT; as a result, there are strong differences in the intensity of blue color. Dichroism ( E || c  ≫  E ⊥ c ) is much stronger in the Kazakhstan sample than in the Norway one. Intensities of the electronic spin-allowed bands of [6] Fe 2+ at ~8900 and ~10,400 cm −1 are somewhat higher in the latter than in the former. FTIR spectra of the sample from Kent show the presence of only water type II molecules with the H–H vector perpendicular to the c -axis, in contrast to more typical beryls that always show at least weak minor bands of H 2 O I. This result shows that trapped water molecules in structural channels of studied bazzite occupy only sites next to or between six-membered rings centered by Na atoms. Definite structure can be observed in the vicinities of ν 2 and ν 3 peaks. Peaks at 1621 and 3663 cm −1 are assigned to “doubly coordinated” H 2 O (IId), whereas maximums at 1633 and 3643 cm −1 likely represent “singly coordinated” H 2 O (IIs). Interpretation of the third components in complex ν 2 and ν 3 bands needs further investigations.</abstract><cop>Berlin/Heidelberg</cop><pub>Springer Berlin Heidelberg</pub><doi>10.1007/s00269-017-0877-2</doi><tpages>11</tpages></addata></record>
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subjects Absorption
Absorption spectra
Aluminum
Aluminum oxide
Atomic structure
Crystallography and Scattering Methods
Dichroism
Earth and Environmental Science
Earth Sciences
Electron probes
Electron spin
Fourier transforms
Geochemistry
Infrared spectroscopy
Iron
Magnesium
Manganese
Mineral Resources
Mineralogy
Mossbauer spectroscopy
Original Paper
Oxidation
Spectrum analysis
Water chemistry
title Optical absorption, Mössbauer, and FTIR spectroscopic studies of two blue bazzites
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