Allantoin and Natrosulfatourea, Two New Bat-Guano Minerals from the Rowley Mine, Maricopa County, Arizona, USA

2021 ◽  
Author(s):  
Anthony R. Kampf ◽  
Aaron J. Celestian ◽  
Barbara P. Nash ◽  
Joe Marty
Keyword(s):  
Crystal Structure ◽  
Optical Orientation ◽  
Chemical Analyses ◽  
Maricopa County ◽  
Conchoidal Fracture ◽  
Urea Group ◽  
Mohs Hardness ◽  
Quantitative Chemical ◽  
White Streak ◽  
Bat Guano

ABSTRACT The new minerals allantoin (IMA2020–004a), C4H6N4O3, and natrosulfatourea (IMA2019–134), Na2(SO4)[CO(NH2)2], were found in the Rowley mine, Maricopa County, Arizona, USA, where they occur together in bat guano in association with aphthitalite and urea. Allantoin properties: colorless, transparent, untwinned blades to 0.3 mm; white streak; vitreous luster; brittle; Mohs hardness 1½; conchoidal fracture; good {100} cleavage; 1.72(2) g/cm3 density; biaxial (+) with α = 1.558(2), β = 1.593(2), γ = 1.715(3); 2V = 60(1)°; slight r > v dispersion; optical orientation: Y = b, Z ^ a = 30° in obtuse β. Natrosulfatourea properties: colorless, transparent, untwinned prisms to 0.3 mm; white streak; vitreous luster; brittle; Mohs hardness 1½; irregular fracture; perfect {100} cleavage; 1.97(2) g/cm3 density; biaxial (+) with α = 1.456(2), β = 1.464(5), γ = 1.524(2); 2V = 42(1)°; no dispersion; optical orientation: X = a, Y = c, Z = b. Quantitative chemical analyses could not be obtained for allantoin. Electron microprobe analyses provided the empirical formula Na2.02(S0.98O4)[CO(NH2)2] for natrosulfatourea. Allantoin is monoclinic, P21/c, a = 8.0304(9), b = 5.1596(5), c = 14.8011(18) Å, β = 93.017(7)°, V = 612.41(11) Å3, and Z = 4. Natrosufatourea is orthorhombic, Pbcn, a = 5.5918(4), b = 18.1814(14), c = 6.7179(5) Å, V = 682.98(9) Å3, and Z = 4. The crystal structure of allantoin (R1 = 0.0432 for 1073 I > 2σI) is the same as that reported for the equivalent organic compound. In the structure of natrosulfatourea (R1 = 0.0413 for 785 I > 2σI) NaO6 polyhedra and SO4 tetrahedra form polyhedral layers. The O atom of the CO(NH2)2 (urea) group ligates to two Na atoms and projects into the space between polyhedral layers, linking adjacent layers through hydrogen bonds.

Badakhshanite-(Y), Y2Mn4Al(Si2B7BeO24), a new mineral species of the perettiite group from a granite miarolic pegmatite in Eastern Pamir, the Gorno Badakhshan Autonomous Oblast, Tajikistan

2020 ◽  
Vol 58 (3) ◽  
pp. 381-394
Author(s):  
Leonid A. Pautov ◽  
Mirak A. Mirakov ◽  
Fernando Cámara ◽  
Elena Sokolova ◽  
Frank C. Hawthorne ◽  
...  
Keyword(s):  
Crystal Structure ◽  
Close Association ◽  
Coarse Grained ◽  
New Mineral ◽  
Orthorhombic Space Group ◽  
Calculated Density ◽  
Conchoidal Fracture ◽  
New Mineral Species ◽  
Mohs Hardness ◽  
Cation Sites

ABSTRACT Badakhshanite-(Y), ideally Y2Mn4Al(Si2B7BeO24), is a tetrahedral sheet-structure mineral found in the Dorozhny (Road) miarolitic granitic pegmatite within the Kukurt pegmatite field 45 km E of Murghab, Eastern Pamir, Gorno-Badakhshan Autonomous Oblast, Tajikistan. Badakhshanite-(Y) occurs in medium- to coarse-grained non-graphic albite-microcline-quartz pegmatites in close association with smoky quartz, Sc-bearing spessartine, Sc-bearing tusionite, and schorl. It often grows together with Sc-bearing tusionite and occurs as single columnar crystals ranging from 50 to 400 μm in length, as inclusions in spessartine and tourmaline, and rarely as crystals in blebs along boundaries between garnet, tourmaline, and quartz. Badakhshanite-(Y) is yellow brown and has a white streak and a vitreous luster. It is brittle, with a conchoidal fracture, Mohs hardness of 6.5–7, and calculated density of 4.41 g/cm. In thin section it is transparent and pale yellow, non-pleochroic, biaxial (–), with α = 1.805(2), βcalc = 1.827, γ = 1.835(3) (λ = 590 nm); 2V (meas.) = –60(10)°. Dispersion is weak, r > v. Extinction is straight, elongation is negative. FTIR spectra show the absence of (OH) and H2O groups. Chemical analysis by electron microprobe using WDS (6 points), SIMS, and ICP-OES for B and Be gave SiO2 11.96, ThO2 0.12, Sm2O3 0.17, Gd2O3 0.30, Tb2O3 0.10, Dy2O3 0.73, Ho2O3 0.19, Er2O3 1.34, Tm2O3 0.54, Yb2O3 8.82, Lu2O3 2.32, Y2O3 16.60, Sc2O3 1.57, Al2O3 3.06, B2O3 22.06, FeO 0.94, MnO 23.33, CaO 0.58, BeO 2.84, total 97.57 wt.%.The empirical formula based on 24 O apfu is (Y1.21REE0.78Th0.01)Σ2(Mn3.47Y0.34Ca0.11Fe2+0.08)Σ4(Al0.63Sc0.24Fe2+0.06□0.07)Σ1[(Si2.10B6.69Be1.20)Σ9.99O24], where REE = (Yb0.47Lu0.12Dy0.04Er0.07Tm0.03 Ho0.01Gd0.02Sm0.01Tb0.01)Σ0.78. Badakhshanite-(Y) is orthorhombic, space group Pnma, a 12.852(1), b 4.5848(5), c 12.8539(8) Å, V 757.38(7) Å3, Z = 2. The crystal structure was refined to R1 = 4.31% based on 1431 unique [F > 4σF] reflections. In the crystal structure of badakhshanite-(Y), a layer of tetrahedra parallel to (010) is composed of four different tetrahedrally coordinated sites: Si, B(1), B(2), and T (<Si–O> = 1.623 Å, <B(1)–O> = 1.485 Å, <B(2)–O> = 1.479 Å, <T–O> = 1.557 Å), which form four-, five-, and eight-membered rings, having the composition (Si2B7BeO24). Between the sheets of tetrahedra, there are three cation sites: M(1), M(2), and M(3) (<M(1)–O> = 2.346 Å, <M(2)–O> = 2.356 Å, <M(3)–O> = 2.016 Å) occupied by Y(REE), Mn2+(Y, Ca, Fe2+), and Al(Sc), respectively. The M(1,2) sites ideally give Y2Mn4apfu; the M(3) site ideally gives Al apfu. Badakhshanite-(Y) is an Al- and Be-analogue of perettiite-(Y).

Magnesiokoritnigite, Mg(AsO3OH)·H2O, from the Torrecillas mine, Iquique Province, Chile: the Mg-analogue of koritnigite

2013 ◽  
Vol 77 (8) ◽  
pp. 3081-3092 ◽  
Author(s):  
A. R. Kampf ◽  
B. P. Nash ◽  
M. Dini ◽  
A. A. Molina Donoso
Keyword(s):  
Powder Diffraction ◽  
Electron Microprobe ◽  
New Mineral ◽  
Optical Orientation ◽  
Secondary Alteration ◽  
X Ray ◽  
Conchoidal Fracture ◽  
Pale Pink ◽  
Perfect Cleavage ◽  
Mohs Hardness

AbstractThe new mineral magnesiokoritnigite (IMA 2013-049), ideally Mg(AsO3OH)·H2O, was found at the Torrecillas mine, Salar Grande, Iquique Province, Chile, where it occurs as a secondary alteration phase in association with anhydrite, chudobaite, halite, lavendulan, quartz and scorodite. Crystals of magnesiokoritnigite are colourless to pale-pink, thin to thick laths up to 2 mm long. Laths are elongated on [001], flattened on {010} and exhibit the forms {010}, {110}, {10}, {101}, {031} and {01}. The crystals also occur in dense deep-pink intergrowths. Crystals are transparent with a vitreous lustre. The mineral has a white streak, Mohs hardness of ∼3, brittle tenacity, conchoidal fracture and one perfect cleavage on {101}. The measured and calculated densities are 2.95(3) and 2.935 g cm– 3, respectively. Optically, magnesiokoritnigite is biaxial (+) with α = 1.579(1), β = 1.586(1) and γ = 1.620(1) (measured in white light). The measured 2V is 50(2)° and the calculated 2V is 50°. Dispersion is r < v, medium. The optical orientation is Y ≈ b; Z ^ c = 36° in obtuse β (note pseudomonoclinic symmetry). The mineral is non-pleochroic. The empirical formula, determined from electron-microprobe analyses, is (Mg0.94Cu0.03Mn0.02Ca0.01)Σ 1.00As0.96O5H3.19. Magnesiokoritnigite is triclinic, P, with a = 7.8702(7), b = 15.8081(6), c = 6.6389(14) Å, α = 90.814(6), β = 96.193(6), γ = 90.094(7)°, V = 821.06(19) Å3 and Z = 8. The eight strongest X-ray powder diffraction lines are [dobs Å (I)(hkl)]: 7.96(100)(020), 4.80(54)(101), 3.791(85)(10,210,1,31), 3.242(56)(02,1,012), 3.157(92)(21,30,230), 3.021(61)(11,141,21,221), 2.798(41)(02,032) and 1.908(43)(multiple). The structure, refined to R1 = 5.74% for 2360 Fo > 4σF reflections, shows magnesiokoritnigite to be isostructural with koritnigite and cobaltkoritnigite.

Phoxite, (NH4)2Mg2(C2O4)(PO3OH)2(H2O)4, the first phosphate-oxalate mineral

2019 ◽  
Vol 104 (7) ◽  
pp. 973-979 ◽  
Author(s):  
Anthony R. Kampf ◽  
Aaron J. Celestian ◽  
Barbara P. Nash ◽  
Joe Marty
Keyword(s):  
Crystal Structure ◽  
Hydrogen Bonds ◽  
New Mineral ◽  
Maricopa County ◽  
New Mineral Species ◽  
Essential Components ◽  
Agricultural Applications ◽  
Mohs Hardness ◽  
Composite Blades ◽  
Natural Pesticide

Abstract Phoxite, (NH4)2Mg2(C2O4)(PO3OH)2(H2O)4, is a new mineral species from the Rowley mine, Maricopa County, Arizona, U.S.A., and it has potential uses in agricultural applications for soil conditioning, fertilizing, and as a natural pesticide. It was found in an unusual bat-guano-related, post-mining assemblage of phases that include a variety of vanadates, phosphates, oxalates, and chlorides, some containing NH4+. Other secondary minerals found in association with phoxite are antipinite, aphithitalite, bassanite, struvite, thenardite, and weddellite. Crystals of phoxite are colorless composite blades up to about 0.4 mm. The streak is white, and the luster is vitreous to oily. The Mohs hardness is 2½, the tenacity is brittle, fracture is irregular, there is fair {100} cleavage, and the measured density is 1.98(2) g/cm3. Phoxite is optically biaxial (–) with α = 1.499(1), β = 1.541(1), γ = 1.542(1) (white light); 2V = 16(1)°; dispersion r < ν, slight; orientation Y = b, X ^ a ≈ 9° in obtuse β. Electron microprobe analyses yielded the empirical formula [(NH4)1.77K0.23]Σ2Mg2.00(C2O4)(PO3OH)2(H2O)4, with the C and H content inferred from the crystal structure. Raman spectroscopy confirmed the presence of NH4 and C2O4. Phoxite is monoclinic, P21/c, with a = 7.2962(3), b = 13.5993(4), c = 7.8334(6) Å, β = 108.271(8)°, V = 738.07(7) Å3, and Z = 2. In the crystal structure of phoxite (R1 = 0.0275 for 1147 Io > 2σI reflections), bidentate linkages between C2O4 groups and Mg-centered octahedra yield chains, which link to one another via PO3OH tetrahedra to create undulating[Mg2(C2O4)(PO3OH)2(H2O)4]2– sheets. Strong hydrogen bonds link the sheets into a “soft framework,” with channels containing NH4+. The NH4+ forms both ordered hydrogen bonds and electrostatic bonds with O atoms in the framework. Phoxite is the first mineral known to contain both phosphate and oxalate groups as essential components.

Hagstromite, Pb8Cu2+(Te6+O6)2(CO3)Cl4, a new lead–tellurium oxysalt mineral from Otto Mountain, California, USA

2020 ◽  
Vol 84 (4) ◽  
pp. 517-523
Author(s):  
Anthony R. Kampf ◽  
Robert M. Housley ◽  
Stuart J. Mills ◽  
George R. Rossman ◽  
Joe Marty
Keyword(s):  
Crystal Structure ◽  
Raman Spectrum ◽  
Electron Microprobe ◽  
Optical Orientation ◽  
Framework Structure ◽  
Secondary Oxidation ◽  
Orthorhombic Space Group ◽  
Calculated Density ◽  
Light Yellow ◽  
Mohs Hardness

AbstractHagstromite, Pb8Cu2+(Te6+O6)2(CO3)Cl4, (IMA2019-093) is a new tellurate mineral from Otto Mountain near Baker, California, USA. It occurs on quartz in association with cerussite, fuettererite and thorneite. It is a secondary oxidation zone mineral and is presumed to have formed by oxidation of earlier formed tellurides, chalcopyrite and galena. Hagstromite occurs as light yellow–green blades, up to ~100 μm long. Crystals are transparent with adamantine to silky lustre. The mineral is brittle with two cleavages providing splintery fracture; the Mohs hardness is probably between 2 and 3. The calculated density is 7.062 g cm–3. Hagstromite is optically biaxial (+), with calculated indices of refraction for α = 2.045, β = 2.066 and γ = 2.102; 2Vmeas = 76(1)°; and optical orientation X = b, Y = a and Z = c. The Raman spectrum of hagstromite exhibits similarities with those of agaite and thorneite and confirms the presence of CO32–. The electron microprobe analyses provided the empirical formula Pb8.07Cu2+0.98Te6+1.96C1.17Cl3.83O15.34. Hagstromite is orthorhombic, space group Ibam, with a = 23.688(17), b = 9.026(8), c = 10.461(8) Å, V = 2237(3) Å3 and Z = 4. The crystal structure of hagstromite (R1 = 0.0659 for 284 I > 2σI reflections) contains a novel Cu2+Te6+2O12 chain assembled of corner-sharing Cu2+O4 squares and Te6+O6 octahedra. The O atoms in the chains form bonds with Pb2+ cations, which in turn bond to Cl– and CO32– anions, thereby creating a framework structure.

Caseyite, a new mineral containing a variant of the flat-Al13 polyoxometalate cation

2020 ◽  
Vol 105 (1) ◽  
pp. 123-131 ◽  
Author(s):  
Anthony R. Kampf ◽  
Mark A. Cooper ◽  
John M. Hughes ◽  
Barbara P. Nash ◽  
Frank C. Hawthorne ◽  
...  
Keyword(s):  
Crystal Structure ◽  
Electron Probe ◽  
Mixed Valence ◽  
New Mineral ◽  
Optical Orientation ◽  
Secondary Mineral ◽  
Calculated Density ◽  
Mineral Assemblages ◽  
Mineral Belt ◽  
Mohs Hardness

Abstract Caseyite, [(V5+O2)Al10–x(OH)20–2x(H2O)18–2x]2[H2V4+V95+O28][V105+O28]2[(Na,K,Ca)2–y(SO4)2–z⋅(60+8x+y+4z) H2O], where x = 0–2.5, y = 0–2, z = 0–2, is a new mineral (IMA 2019-002) occurring in low-temperature, post-mining, secondary mineral assemblages at the Burro, Packrat, and West Sunday mines in the Uravan Mineral Belt of Colorado, U.S.A. Crystals of caseyite are yellow tapering needles or blades, with a pale yellow streak, vitreous luster, brittle tenacity, curved fracture, no cleavage, Mohs hardness between 2 and 3, and 2.151 g/cm3 calculated density. Caseyite is optically biaxial (+) with α = 1.659(3), β = 1.670(3), γ = 1.720(3) (white light), 2V = 52.6(5)°, has strong r &lt; ν dispersion, optical orientation Z ≈ a (elongation of needles), and no pleochroism. Electron-probe microanalysis provided the empirical formula [(V5+O2)Al8.94(OH)17.88(H2O)15.88]2[H2V4+V95+O28][V105+O28]2[(Na0.82Ca0.35K0.27)Σ1.44 (SO4)1.33⋅70.24H2O] (+0.94 H). Caseyite is monoclinic, P21/n, a = 14.123(8), b = 30.998(15), c = 21.949(11) Å, β = 97.961(8)°, V = 9516(9) Å3, and Z = 2. The crystal structure (R1 = 0.0654 for 9162 Io&gt;2σI reflections) contains both normal [V10O28]6– and doubly protonated mixed-valence [H2V14+V95+O28]5– decavanadate isopolyanions, and a novel vanadoaluminate heteropolycation (“flat-Al10V☐2”), ideally [(V5+O2)Al10(OH)20(H2O)18]11+, closely related to the technologically important flat-Al13 polyoxocation.

scholarly journals Kyawthuite, Bi3+Sb5+O4, a new gem mineral from Mogok, Burma (Myanmar)

2017 ◽  
Vol 81 (3) ◽  
pp. 477-484 ◽  
Author(s):  
Anthony R. Kampf ◽  
George R. Rossman ◽  
Chi Ma ◽  
Peter A. Williams
Keyword(s):  
Monoclinic Space Group ◽  
Optical Orientation ◽  
X Ray Diffraction ◽  
Calculated Density ◽  
Electron Pairs ◽  
X Ray ◽  
Conchoidal Fracture ◽  
Cell Dimensions ◽  
Mohs Hardness ◽  
Unit Cell Dimensions

AbstractKyawthuite, Bi3+Sb5+O4, is a new gem mineral found as a waterworn crystal in alluvium at Chaung-gyi-ah-le-ywa in the Chaung-gyi valley, near Mogok, Burma (Myanmar). Its description is based upon a single sample, which was faceted into a 1.61-carat gem.The composition suggests that the mineral formed in a pegmatite. Kyawthuite is monoclinic, space group I2/c, with unit cell dimensions a = 5.4624(4), b = 4.88519(17), c = 11.8520(8) Å, β = 101.195(7)°, V = 310.25(3) Å3and Z = 4. The colour is reddish orange and the streak is white. It is transparent with adamantine lustre. The Mohs hardness is 5½. Kyawthuite is brittle with a conchoidal fracture and three cleavages: {001} perfect, {110} and {110} good. The measured density is 8.256(5) g cm–3and the calculated density is 8.127 g cm–3. The mineral is optically biaxial with 2V = 90(2)°. The predicted indices of refraction are α = 2.194, β = 2.268, γ = 2.350. Pleochroism is imperceptible and the optical orientation is X = b; Y≈ c; Z ≈ a. Electron microprobe analyses, provided the empirical formula (Bi0.823+Sb0.183+)∑1.00(Sb0.995+Ta0.015+)∑1.00O4. The Raman spectrumis similar to that of synthetic Bi3+Sb5+O4. The infrared spectrum shows a trace amount of OH/H2O. The eight strongest powder X-ray diffraction lines are [dobs in Å(I)(hkl)]: 3.266(100)(112), 2.900(66)(112), 2.678(24)(200), 2.437(22)(020,114), 1.8663(21)(024), 1.8026(43)(116,220,204), 1.6264(23)(224,116) and 1.5288(28)(312,132). In the crystal structure of kyawthuite (R1 = 0.0269 for 593 reflections with Fo > 4σF), Sb5+O6 octahedrashare corners to form chequerboard-like sheets parallel to {001}. Atoms of Bi3+, located above and below the open squares in the sheets, form bonds to the O atoms in the sheets, thereby linking adjacent sheets into a framework. The Bi3+ atom is in lopsided 8 coordination,typical of a cation with stereoactive lone electron pairs. Kyawthuite is isostructural with synthetic β-Sb2O4 and clinocervantite (natural β-Sb2O4).

Hingganite-(Nd), Nd2□Be2Si2O8(OH)2, a new gadolinite-supergroup mineral from Zagi Mountain, Pakistan

2020 ◽  
Vol 58 (5) ◽  
pp. 549-562
Author(s):  
Anatoly V. Kasatkin ◽  
Fabrizio Nestola ◽  
Radek Škoda ◽  
Nikita V. Chukanov ◽  
Atali A. Agakhanov ◽  
...  
Keyword(s):  
New Mineral ◽  
Monoclinic Space Group ◽  
X Ray Diffraction ◽  
Average Chemical Composition ◽  
X Ray ◽  
Conchoidal Fracture ◽  
Icp Ms ◽  
Optical Axes ◽  
Mohs Hardness ◽  
Khyber Pakhtunkhwa Province

ABSTRACT Hingganite-(Nd), ideally Nd2□Be2Si2O8(OH)2, is a new gadolinite group, gadolinite supergroup mineral discovered at Zagi Mountain, near Kafoor Dheri, about 4 km S of Warsak and 30 km NW of Peshawar, Khyber Pakhtunkhwa Province, Pakistan. The new mineral forms zones measuring up to 1 × 1 mm2 in loose prismatic crystals up to 0.7 cm long, where it is intergrown with hingganite-(Y). Other associated minerals include aegirine, microcline, fergusonite-(Y), and zircon. Hingganite-(Nd) is dark greenish-brown, transparent, has vitreous luster and a white streak. It is brittle and has a conchoidal fracture. No cleavage or parting are observed. Mohs hardness is 5½–6. Dcalc. = 4.690 g/cm3. Hingganite-(Nd) is non-pleochroic, optically biaxial (+), α = 1.746(5), β = 1.766(5), γ = 1.792(6) (589 nm). 2Vmeas. = 80(7)°; 2Vcalc. = 84°. Dispersion of optical axes was not observed. The average chemical composition of hingganite-(Nd) is as follows (wt.%; electron microprobe, BeO, B2O3, and Lu2O3 content measured by LA-ICP-MS; H2O calculated by stoichiometry): BeO 9.64, CaO 0.45, MnO 0.10, FeO 3.03, B2O3 0.42, Y2O3 8.75, La2O3 1.63, Ce2O3 12.89, Pr2O3 3.09, Nd2O3 16.90, Sm2O3 5.97, Eu2O3 1.08, Gd2O3 5.15, Tb2O3 0.50, Dy2O3 2.50, Ho2O3 0.33, Er2O3 0.84, Tm2O3 0.10, Yb2O3 0.44, Lu2O3 0.04, ThO2 0.13, SiO2 23.55, H2O 2.72, total 100.25. The empirical formula calculated on the basis of 2 Si apfu is (Nd0.513Ce0.401Y0.395Sm0.175Gd0.145Pr0.096Dy0.068La0.051Ca0.041Eu0.031Er0.022Tb0.014Yb0.011Ho0.009Tm0.003Th0.003Lu0.001)Σ1.979(□0.778Fe2+0.215Mn0.007)Σ1.000(Be1.967B0.062)Σ2.029Si2O8.46(OH)1.54. Hingganite-(Nd) is monoclinic, space group P21/c with a = 4.77193(15), b = 7.6422(2), c = 9.9299(2) Å, β = 89.851(2)°, V = 362.123(14) Å3, and Z = 2. The strongest lines of the powder X-ray diffraction pattern [d, Å (I, %) (hkl)] are: 6.105 (95) (011), 4.959 (56) (002), 4.773 (100) (100), 3.462 (58) (102), 3.122 , 3.028 (61) (013), 2.864 (87) (121), 2.573 (89) (113). The crystal structure of hingganite-(Nd) was refined from single-crystal X-ray diffraction data to R = 0.034 for 2007 unique reflections with I &gt; 2σ(I). The new mineral is named as an analogue of hingganite-(Y), hingganite-(Yb), and hingganite-(Ce), but with Nd dominant among the rare earth elements.

scholarly journals Physicochemical and structural characteristics of HEU-type zeolitic tuff treated by hydrochloric acid

2004 ◽  
Vol 69 (4) ◽  
pp. 273-282 ◽  
Author(s):  
Ana Radosavljevic-Mihajlovic ◽  
Vera Dondur ◽  
Aleksandra Dakovic ◽  
Jovan Lemic ◽  
Magdalena Tomasevic-Canovic
Keyword(s):  
Crystal Structure ◽  
Hydrochloric Acid ◽  
Bosnia And Herzegovina ◽  
Acid Treatment ◽  
Structural Characteristics ◽  
Chemical Analyses ◽  
Zeolitic Tuff ◽  
Zeolitic Tuffs ◽  
Before And After

Samples of natural HEU-type zeolites ? clinoptilolite-Ca, from the Novakovici deposit (near Prijedor, Bosnia and Herzegovina) were treated with the hydrochloric acid of various concentrations (from 10-3Mto 2M). Zeolitic tuffs before and after the acid treatment were examined using IR, XRPD, and chemical analyses. The changes in the crystal structure of acid treated samples showed a significant reduction in the crystallinity of zeolitic tuffs (60?70 %), which were effected by hydrochloric acid with concentrations of 1 M and above.

scholarly journals Chirvinskyite, (Na,Ca)13(Fe,Mn,□)2(Ti,Nb)2(Zr,Ti)3-(Si2O7)4(OH,O,F)12, a New Mineral with a Modular Wallpaper Structure, from the Khibiny Alkaline Massif (Kola Peninsula, Russia)

Minerals ◽  
2019 ◽  
Vol 9 (4) ◽  
pp. 219
Author(s):  
Victor Yakovenchuk ◽  
Yakov Pakhomovsky ◽  
Taras Panikorovskii ◽  
Andrey Zolotarev ◽  
Julia Mikhailova ◽  
...  
Keyword(s):  
Kola Peninsula ◽  
Empirical Formula ◽  
Inorganic Compounds ◽  
Structure Type ◽  
New Mineral ◽  
State University ◽  
Mohs Hardness ◽  
Alkaline Massif ◽  
Khibiny Alkaline Massif ◽  
White Streak

Chirvinskyite, (Na,Ca)13(Fe,Mn,□)2(Ti,Nb)2(Zr,Ti)3(Si2O7)4(OH,O,F)12, is a new wöhlerite–related zirconotitano–sorosilicate. It is triclinic, P1, a = 7.0477(5), b = 9.8725(5), c = 12.2204(9) Å, α = 77.995(5), β = 82.057(6), γ = 89.988(5)°, V = 823.35(9) Å3, Z = 1. The mineral was found in albitized alkaline pegmatites in a foyaite of the Mt. Takhtarvumchorr (Khibiny alkaline massif, Kola Peninsula, Russia, N 67°40’, E 33°33’). Chirvinskyite forms sheaf–like and radiated aggregates (up to 6 mm in diameter) of split fibrous crystals hosted by saccharoidal fluorapatite and albite. The mineral is pale cream in color, with a silky luster and a white streak. The cleavage is not recognized. Mohs hardness is 5. Chirvinskyite is biaxial (–), α 1.670(2), β 1.690(2), γ 1.705(2) (589 nm), 2Vcalc = 80.9°. The calculated and measured densities are 3.41 and 3.07(2) g·cm−3, respectively. The empirical formula based on Si = 8 apfu is (Na9.81Ca3.28K0.01)∑13.10(Fe0.72Mn0.69□0.54Mg0.05)∑2.00 (Ti1.81Nb0.19)∑2.00(Zr2.27Ti0.63)∑2.90(Si2O7)4{(OH)5.94O3.09F2.97}∑12.00. Chirvinskyite belongs to a new structure type of minerals and inorganic compounds and is related to the wöhlerite-group minerals. Its modular “wallpaper” structure consists of disilicate groups Si2O7 and three types of “octahedral walls”. The mineral is named in honor of Petr Nikolaevich Chirvinsky (1880–1955), Russian geologist and petrographer, head of the Petrography Department of the Perm’ State University (1943–1953), for his contributions to mineralogy and petrology, including studies of the Khibiny alkaline massif.

Kihlmanite-(Ce), Ce2TiO2[SiO4](HCO3)2(H2O), a new rare-earth mineral from the pegmatites of the Khibiny alkaline massif, Kola Peninsula, Russia

2014 ◽  
Vol 78 (3) ◽  
pp. 483-496 ◽  
Author(s):  
V. N. Yakovenchuk ◽  
S.V. Krivovichev ◽  
G. Y. Ivanyuk ◽  
Ya. A. Pakhomovsky ◽  
E.A. Selivanova ◽  
...  
Keyword(s):  
Crystal Structure ◽  
Rare Earth ◽  
Powder Diffraction ◽  
Diffraction Data ◽  
X Ray ◽  
Intimate Association ◽  
Mohs Hardness ◽  
Rare Earth Mineral ◽  
Alkaline Massif ◽  
Khibiny Alkaline Massif

AbstractKihlmanite-(Ce), Ce2TiO2[SiO4](HCO3)2(H2O), is a new rare-earth titanosilicate carbonate, closely related to tundrite-(Ce). It is triclinic, P, a = 4.994(2), b = 7.54(2), c = 15.48(4) Å, α = 103.5(4), β = 90.7(2), γ = 109.2(2)o , V = 533(1) Å3, Z = 2 (from powder diffraction data) or a = 5.009(5), b = 7.533(5), c = 15.407(5) Å, α = 103.061(5), β = 91.006(5), γ = 109.285(5)°, V = 531.8(7) Å3, Z = 2 (from single-crystal X-ray diffraction data). The mineral was found in the arfvedsonite-aegirine-microcline vein in fenitized metavolcanic rock at the foot of the Mt Kihlman (Chil’man), near the western contact of the Devonian Khibiny alkaline massif and the Proterozoic Imandra-Varzuga greenstone belt. It forms brown spherulites (up to 2 cm diameter) and sheaf-like aggregates of prismatic crystals, flattened on {010} and up to 0.5 mm diameter. Both spherulites and aggregates occur in interstices in arfvedsonite and microcline, in intimate association with golden-green tundrite-(Ce). Kihlmanite-(Ce) is brown, with a vitreous lustre and a pale yellowish-brown streak. The cleavage is perfect on {010}, parting is perpendicular to c and the fracture is stepped. Mohs hardness is ∼3. In transmitted light, the mineral is yellowish brown; pleochroism and dispersion were not observed. Kihlmanite-(Ce) is biaxial (+), α = 1.708(5), β = 1.76(1), γ = 1.82(1) (589 nm), 2Vcalc = 89°. The optical orientation is Y ^ c = 5°, other details are unclear. The calculated and measured densities are 3.694 and 3.66(2) g cm−3, respectively. The mean chemical composition, determined by electron microprobe, is: Na2O 0.13, Al2O3 0.24, SiO2 9.91, CaO 1.50, TiO2 11.04, MnO 0.26, Fe2O3 0.05, Nb2O5 2.79, La2O3 12.95, Ce2O3 27.33, Pr2O3 2.45, Nd2O3 8.12, Sm2O3 1.67, Gd2O3 0.49 wt.%, with CO2 15.0 and H2O 6.0 wt.% (determined by wet chemical and Penfield methods, respectively), giving a total of 99.93 wt.%. The empirical formula calculated on the basis of Si + Al = 1 atom per formula unit is (Ca0.16Na0.11Mn0.02)∑0.29[(Ce0.98La0.47Pr0.09Nd0.29Sm0.06Gd0.02)∑1.91(Ti0.82Nb0.12)∑0.94O2 (Si0.97Al0.03)∑1O4.02(HCO3)2.01](H2O)0.96. The simplified formula is Ce2TiO2(SiO4)(HCO3)2·H2O. The mineral reacts slowly in cold 10% HCl with weak effervescence and fragmentation into separate plates. The strongest X-ray powder-diffraction lines [listed as d in Å(I) (hkl)] are as follows: 15.11(100)(00), 7.508(20)(00), 6.912(12)(01), 4.993(14)(00), 3.563(15)(01), 2.896(15)(1). The crystal structure of kihlmanite-(Ce) was refined to R1 = 0.069 on the basis of 2441 unique observed reflections (MoKα, 293 K). It is closely related to the crystal structure of tundrite-(Ce) and is based upon [Ce2TiO2(SiO4)(HCO3)2] layers parallel to (001). Kihlmanite-(Ce) can be considered as a cationdeficient analogue of tundrite-(Ce). The mineral is named in honour of Alfred Oswald Kihlman (1858–1938), a remarkable Finnish geographer and botanist who participated in the Wilhelm Ramsay expeditions to the Khibiny Mountains in 1891–1892. The mineral name also reflects its occurrence at the Kihlman (Chil’man) Mountain.

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