Materials Map

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The Materials Map is an open tool for improving networking and interdisciplinary exchange within materials research. It enables cross-database search for cooperation and network partners and discovering of the research landscape.

The dashboard provides detailed information about the selected scientist, e.g. publications. The dashboard can be filtered and shows the relationship to co-authors in different diagrams. In addition, a link is provided to find contact information.

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The Materials Map is still under development. In its current state, it is only based on one single data source and, thus, incomplete and contains duplicates. We are working on incorporating new open data sources like ORCID to improve the quality and the timeliness of our data. We will update Materials Map as soon as possible and kindly ask for your patience.

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in Cooperation with on an Cooperation-Score of 37%

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Publications (11/11 displayed)

  • 2022Polytypism in mcalpineite: a study of natural and synthetic Cu3TeO610citations
  • 2021Kernowite, Cu<sub>2</sub>Fe(AsO<sub>4</sub>)(OH)<sub>4</sub>⋅4H<sub>2</sub>O, the Fe<sup>3+</sup>-analogue of liroconite from Cornwall, UK1citations
  • 2021Oscillatory- and sector-zoned pyrochlore from carbonatites of the Kerimasi volcano, Gregory rift, Tanzania13citations
  • 2021Elucidating the natural–synthetic mismatch of Pb2+Te4+O3: The redefinition of fairbankite to Pb122+(Te4+O3)11(SO4)2citations
  • 2021Native tungsten from the Bol'shaya Pol'ya river valley and Mt Neroyka, Russiacitations
  • 2021Wildcatite, CaFe3+Te6+O5(OH), the second new tellurate mineral from the Detroit district, Juab County, Utah1citations
  • 2021Hybridization of Alkali Basaltic Magmas: a Case Study of the Ogol Lavas from the Laetoli Area, Crater Highlands (Tanzania)1citations
  • 2019Dokuchaevite, Cu<sub>8</sub>O<sub>2</sub>(VO<sub>4</sub>)<sub>3</sub>Cl<sub>3</sub>, a new mineral with remarkably diverse Cu<sup>2+</sup> mixed-ligand coordination environments14citations
  • 2019The crystal structures of the mixed-valence tellurium oxysalts tlapallite, (Ca,Pb)<sub>3</sub>CaCu<sub>6</sub>[Te<sup>4+</sup><sub>3</sub>Te<sup>6+</sup>O<sub>12</sub>]<sub>2</sub>(Te<sup>4+</sup>O<sub>3</sub>)<sub>2</sub>(SO<sub>4</sub>)<sub>2</sub>·3H<sub>2</sub>O, and carlfriesite, CaTe<sup>4+</sup><sub>2</sub>Te<sup>6+</sup>O<sub>8</sub>8citations
  • 2015Barrydawsonite-(Y), Na<sub>1.5</sub>CaY<sub>0.5</sub>Si<sub>3</sub>O<sub>9</sub>H: a new pyroxenoid of the pectolite–serandite group8citations
  • 2013Diegogattaite, Na<sub>2</sub>CaCu<sub>2</sub>Si<sub>8</sub>O<sub>2</sub>0·H<sub>2</sub>O: a new nanoporous copper sheet silicate from Wessels Mine, Kalahari Manganese Fields, Republic of South Africa9citations

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Mills, Stuart J.
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Hadermann, Joke
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Missen, Owen P.
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Libowitzky, Eugen
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Rumsey, Michael S.
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Artner, Werner
1 / 1 shared
Housley, Robert M.
1 / 1 shared
Canossa, Stefano
1 / 3 shared
Weil, Matthias
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Dunstan, Maja
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Nénert, Gwilherm
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Mccormack, John K.
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Kampf, Anthony R.
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Marty, Joe
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Raudsepp, Mati
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Najorka, Jens
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Coolbaugh, Mark F.
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Zaitsev, Anatoly N.
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Marks, Michael A. W.
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Markl, Gregor
1 / 1 shared
Wenzel, Thomas
1 / 1 shared
Braunger, Simon
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Salge, Tobias
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Co-Authors (by relevance)

  • Mills, Stuart J.
  • Hadermann, Joke
  • Missen, Owen P.
  • Libowitzky, Eugen
  • Rumsey, Michael S.
  • Artner, Werner
  • Housley, Robert M.
  • Canossa, Stefano
  • Weil, Matthias
  • Dunstan, Maja
  • Nénert, Gwilherm
  • Mccormack, John K.
  • Kampf, Anthony R.
  • Marty, Joe
  • Raudsepp, Mati
  • Najorka, Jens
  • Coolbaugh, Mark F.
  • Zaitsev, Anatoly N.
  • Marks, Michael A. W.
  • Markl, Gregor
  • Wenzel, Thomas
  • Braunger, Simon
  • Salge, Tobias
OrganizationsLocationPeople

article

Barrydawsonite-(Y), Na<sub>1.5</sub>CaY<sub>0.5</sub>Si<sub>3</sub>O<sub>9</sub>H: a new pyroxenoid of the pectolite–serandite group

  • Spratt, John
Abstract

<jats:title>Abstract</jats:title><jats:p>The new pyroxenoid barrydawsonite-(Y) occurs at the Merlot Claim, North Red Wine Pluton, Labrador, Canada (62°32'38.54'' W; 54°08'1.37'' N). The host rock is a metamorphosed eudialyte syenite consisting of eudialyte, potassic arfvedsonite, jadeitic aegirine, nepheline, albite and potassium feldspar with accessory Y-bearing pectolite, britholite and steenstrupine. Barrydawsonite-(Y) crystals commonly have discrete thin rims of Y-bearing pectolite. The average empirical formula (based on nine anions p.f.u.) is Na<jats:sub>1.54</jats:sub>Ca<jats:sub>0.74</jats:sub>Mn<jats:sub>0.15</jats:sub>Fe<jats:sub>0.07</jats:sub>Y<jats:sub>0.38</jats:sub>Nd<jats:sub>0.01</jats:sub>Sm<jats:sub>0.01</jats:sub>Gd<jats:sub>0.02</jats:sub>Tb<jats:sub>0.01</jats:sub>Dy<jats:sub>0.04</jats:sub>Ho<jats:sub>0.01</jats:sub>Er<jats:sub>0.02</jats:sub>Yb<jats:sub>0.01</jats:sub>Si<jats:sub>3.00</jats:sub>O<jats:sub>9</jats:sub>H. The simplified formula is Na<jats:sub>1.5</jats:sub>Y<jats:sub>0.5</jats:sub>CaSi<jats:sub>3</jats:sub>O<jats:sub>9</jats:sub>H. Barrydawsonite-(Y) is related to pectolite by the substitution ½[Na<jats:italic>M</jats:italic><jats:sup>3+</jats:sup>Ca<jats:sub>–2</jats:sub>] (<jats:italic>M</jats:italic><jats:sup>3+</jats:sup>= Y,<jats:italic>REE</jats:italic>), and is exceptional in being the only member of the pectolite group that has the structure of the monoclinic<jats:italic>M2abc</jats:italic>polytype. The crystal structure has been determined in monoclinic space group<jats:italic>P</jats:italic>2<jats:sub>1</jats:sub>/<jats:italic>a: a</jats:italic>= 15.5026(2),<jats:italic>b</jats:italic>= 7.0233(1),<jats:italic>c</jats:italic>= 6.9769(1) Å, β = 95.149(1)°,<jats:italic>V</jats:italic>= 756.58(2) Å<jats:sup>3</jats:sup>(<jats:italic>Z</jats:italic>= 4). Final agreement indices are<jats:italic>R</jats:italic><jats:sub>1</jats:sub>= 0.038,<jats:italic>wR</jats:italic><jats:sub>2</jats:sub>= 0.068, Goof = 1.136. The asymmetric unit of barrydawsonite-(Y) has three metal sites:<jats:italic>M</jats:italic>(1) = Ca,<jats:italic>M</jats:italic>(2) = Na0.5(Y,REE)0.5,<jats:italic>M</jats:italic>(3) = Na.<jats:italic>M</jats:italic>(1) and<jats:italic>M</jats:italic>(2) are octahedrally-coordinated sites, whereas<jats:italic>M</jats:italic>(3) is [8]-coordinated as in pectolite and serandite. The structural formula for the empirical composition is<jats:sup><jats:italic>M</jats:italic>(3)</jats:sup>Na<jats:sub>1.00</jats:sub><jats:sup><jats:italic>M</jats:italic>(2)</jats:sup>(Na<jats:sub>0.50</jats:sub>Y<jats:sub>0.38</jats:sub><jats:italic>REE</jats:italic><jats:sub>0.13</jats:sub>)<jats:sub>Σ=1.01</jats:sub><jats:sup><jats:italic>M</jats:italic>(1)</jats:sup>(Na<jats:sub>0.04</jats:sub>Ca<jats:sub>0.74</jats:sub>Mn<jats:sub>0.15</jats:sub><jats:sup>2+</jats:sup>Fe<jats:sub>0.07</jats:sub><jats:sup>2+</jats:sup>)<jats:sub>Σ=1.00</jats:sub>Si<jats:sub>3</jats:sub>O<jats:sub>9</jats:sub>H. There is excellent agreement between the refined site-scattering values and those calculated based upon the structural formula.</jats:p><jats:p>Barrydawsonite-(Y) is biaxial (+) with α = 1.612(1), β = 1.617(1), γ = 1.630(1) (white light) and 2V = 63(1)°. The five strongest peaks in the X-ray powder diffraction pattern are [<jats:italic>d</jats:italic><jats:sub>obs</jats:sub>(Å),<jats:italic>I</jats:italic><jats:sub>obs</jats:sub>%, (hkl)]: [2.905, 100, (023)], [3.094, 30, (210,211,121,202)], [1.7613, 29, (127,323,040)], [3.272, 27, (202,104)], [1.7016, 27, (140,227,325)].</jats:p>

Topics
  • impedance spectroscopy
  • Potassium
  • space group