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  • 1
    Online Resource
    Online Resource
    Royal Society of Chemistry (RSC) ; 1959
    In:  Journal of the Chemical Society (Resumed) ( 1959), p. 2303-
    In: Journal of the Chemical Society (Resumed), Royal Society of Chemistry (RSC), ( 1959), p. 2303-
    Type of Medium: Online Resource
    ISSN: 0368-1769
    RVK:
    Language: English
    Publisher: Royal Society of Chemistry (RSC)
    Publication Date: 1959
    detail.hit.zdb_id: 215831-0
    detail.hit.zdb_id: 2197229-1
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  • 2
    Online Resource
    Online Resource
    Mineralogical Society ; 2005
    In:  Mineralogical Magazine Vol. 69, No. 2 ( 2005-04), p. 145-153
    In: Mineralogical Magazine, Mineralogical Society, Vol. 69, No. 2 ( 2005-04), p. 145-153
    Abstract: Tiny green crystals from Kabwe, Zambia, associated with hopeite and tarbuttite (and probably first recorded in 1908 but never adequately characterized because of their scarcity) have been studied by X-ray diffraction, microchemical and electron probe microanalysis, infrared spectroscopy, and synthesis experiments. They are shown to be orthorhombic, stoichiometric CuZnPO 4 OH, of species rank, forming the end-member of a solid-solution series to libethenite, Cu 2 PO 4 OH, and are named zincolibethenite. The libethenite structure is unwilling to accommodate any more Zn substituting for Cu at atmospheric pressure, syntheses using Zn-rich solutions precipitating a mixture of zincolibethenite with hopeite, Zn 3 (PO 4 ) 2 .4H 2 O. Single-crystal X-ray data confirm that the Cu(II) occupies the Jahn-Teller distorted 6-coordinate cation site in the libethenite lattice, and the Zn(II) occupies the 5-coordinate site. The space group of zincolibethenite is Pnnm , the same as that of libethenite, with unit-cell parameters a = 8.326, b = 8.260, c = 5.877 Å , V = 404.5 Å 3 , Z = 4, calculated density = 3.972 g/cm 3 (libethenite has a = 8.076, b = 8.407, c = 5.898 Å , V = 400.44 Å 3 , Z = 4, calculated density = 3.965 g/cm 3 ). Zincolibethenite is biaxial negative, with 2V α (calc.) of 49°, r 〈 v , and α = 1.660, β = 1.705, and γ = 1.715 The mineral is named for its relationship to libethenite.
    Type of Medium: Online Resource
    ISSN: 0026-461X , 1471-8022
    RVK:
    Language: English
    Publisher: Mineralogical Society
    Publication Date: 2005
    detail.hit.zdb_id: 2034522-7
    SSG: 13
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  • 3
    Online Resource
    Online Resource
    Mineralogical Society ; 1973
    In:  Mineralogical Magazine Vol. 39, No. 304 ( 1973-12), p. 401-411
    In: Mineralogical Magazine, Mineralogical Society, Vol. 39, No. 304 ( 1973-12), p. 401-411
    Abstract: ‘Blue John’ andother purple fluorites have been studied by a wide range of techniques. Hydrocarbons are not the cause of the colour of these fluorites. No significant difference in the concentrations of 73 elements between the purple and colourless zones of Blue John has been detected. The spectroscopic and thermal bleaching behaviour of the purple zones is consistent with the presence of ‘colloidal’ calcium as colouring agent, and coloration of fluorites with calcium vapour gives material showing similar properties. The distribution of colour suggests trapping of the calcium in lattice defects along {111} (cleavage) planes through {001} (growth) zones. The ‘colloids’ could be produced by aggregation of calcium atoms liberated by irradiation from sources found in the geological environment of Blue John. The banding could arise from variations in the concentration of lattice defects caused by variations in growth rates of the fluorite.
    Type of Medium: Online Resource
    ISSN: 0026-461X , 1471-8022
    RVK:
    Language: English
    Publisher: Mineralogical Society
    Publication Date: 1973
    detail.hit.zdb_id: 2034522-7
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  • 4
    Online Resource
    Online Resource
    Mineralogical Society ; 1994
    In:  Mineralogical Magazine Vol. 58, No. 390 ( 1994-03), p. 79-85
    In: Mineralogical Magazine, Mineralogical Society, Vol. 58, No. 390 ( 1994-03), p. 79-85
    Abstract: Iowaite has been re-examined using new, well crystallized material from the Palabora open pit mine, Transvaal. Microprobe, carbon analyser and thermal analyses, powder and single-crystal X-ray diffraction, infrared, UV-visible and mass spectroscopic and optical studies were made. The ideal formula is (OH) 16 Cl 2 ·4H 2 O. It is trigonal, R 3̄ m , a = 3.1183(9), c = 24.113(8) Å, V = 203.1(2) Å 3 , Z = 3/8; D obs 2.09 g/cm 3. ; D calc 2.04 g/cm 3 ; hardness (Mohs)=2 1/2. The interlayer Cl − ions are displaced from the threefold axis. It is uniaxial negative, with ω = 1.561 ± 0.002, ε = 1.543 ± 0.002; coloured crystals are intensely pleochroic, due to intervalence charge transfer between the Fe 3+ and Fe 2+ substituting for Mg 2+ , with O pale yellow, E deep blue-green.
    Type of Medium: Online Resource
    ISSN: 0026-461X , 1471-8022
    RVK:
    Language: English
    Publisher: Mineralogical Society
    Publication Date: 1994
    detail.hit.zdb_id: 2034522-7
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  • 5
    Online Resource
    Online Resource
    Springer Science and Business Media LLC ; 1992
    In:  Mineralogy and Petrology Vol. 47, No. 2-4 ( 1992), p. 255-261
    In: Mineralogy and Petrology, Springer Science and Business Media LLC, Vol. 47, No. 2-4 ( 1992), p. 255-261
    Type of Medium: Online Resource
    ISSN: 0930-0708 , 1438-1168
    RVK:
    Language: English
    Publisher: Springer Science and Business Media LLC
    Publication Date: 1992
    detail.hit.zdb_id: 1462900-8
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  • 6
    Online Resource
    Online Resource
    Mineralogical Society ; 2009
    In:  Mineralogical Magazine Vol. 73, No. 5 ( 2009-10), p. 871-881
    In: Mineralogical Magazine, Mineralogical Society, Vol. 73, No. 5 ( 2009-10), p. 871-881
    Abstract: Daliranite, ideally PbHgAs 2 S 6 , a new sulphosalt from the Zarshouran Au-As deposit, Takab region, Iran, occurs as a rare sulphosalt species at the Carlin-type Zarshouran Au-As deposit North of the town of Takab in the Province of West Azarbaijan, Iran. The new species is associated with orpiment, rarely with galkhaite, hutchinsonite and cinnabar. The strongly silicified matrix of the specimens has veinlets of sphalerite, with rare inclusions of galena and various (Cu)-Pb-As(Sb) sulphosalts. Daliranite occurs as matted nests of acicular and flexible fibres up to 200 μm in length and a width less than a few μm. The colour is orange-red with a pale orange-red streak and the lustre is adamantine. The mineral is transparent and does not fluoresce. The Mohs hardness is 〈 2. Electron microprobe analyses give the empirical formula Pb 0.95 Tl 0.01 Hg 1.04 As 2.10 S 5.91 , ideally PbHgAs 2 S 6 , a new sulphosalt from the Zarshouran Au-As deposit, Takab region, Iran; the calculated density is 5.93 g cm –3 . Unit-cell parameters were determined by an electron-diffraction study and refined from X-ray powder data. Daliranite is monoclinic primitive with a = 19.113(5) Å, b = 4.233(2) Å, c = 22.958(8) Å, β = 114.78(5)°, V = 1686.4 Å 3 and Z = 8, a:b:c = 4.515:1:5.424, space group P 2, Pm or P 2/ m . The strongest X-ray powder-diffraction lines [ d in Å, ( I ), ( hkl )] are: 8.676, (80), (200); 4.654, (50), (401); 3.870, (40), (211); 3.394, (50), (113); 3.148, (40b), (602); 2.892, (50), (600); 2.724, (100), (703); 2.185, (50), (319). The formula shows a sulphur excess which may correspond to S—S bonding (persulphide). The new sulphosalt is a late phase in the crystallization sequenc e, and was formed after orpiment, contemporaneously with quartz II, at a temperature between 157 and 193°C. The name honours Dr Farahnaz Daliran (University of Karlsruhe, Germany) in recognition of her outstanding contributions to research on ore deposits, especially Au, Zn and Fe, in Iran.
    Type of Medium: Online Resource
    ISSN: 0026-461X , 1471-8022
    RVK:
    Language: English
    Publisher: Mineralogical Society
    Publication Date: 2009
    detail.hit.zdb_id: 2034522-7
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  • 7
    Online Resource
    Online Resource
    Mineralogical Society ; 1986
    In:  Mineralogical Magazine Vol. 50, No. 355 ( 1986-03), p. 129-135
    In: Mineralogical Magazine, Mineralogical Society, Vol. 50, No. 355 ( 1986-03), p. 129-135
    Abstract: Chenite, a new lead-copper secondary mineral, has been found on specimens from the Leadhills area, Scotland. It is associated with caledonite, linarite, leadhillite, susannite, and other species, on oxidized galena with chalcopyrite. Electron microprobe analysis yielded PbO 74.5, CuO 7.8, SO 3 13.3, H 2 O 4.4 (by difference), sum = 100 wt. %. The empirical formula (based on 14 oxygens) is Pb 3.98 Cu 1.17 S 1.98 O 14 H 5.82 ; the ideal formula is Pb 4 Cu(SO 4 ) 2 (OH) 6 , which requires PbO 75.2, CuO 6.7, SO 3 13.5, H 2 O 4.6, sum = 100 wt. %. Infra-red spectroscopy showed the presence of only and OH − ions, with no H 2 O. Chenite is triclinic, P 1 or P ̄, with a = 5.791(1), b = 7.940(1), c = 7.976(1) Å, α = 112.02(1), β = 97.73(1), γ = 100.45(1)°, V = 326.0 Å 3 , Z = 1. The strongest lines in the X-ray powder diffraction pattern ( d, I/I o , hkl ) are: 5.55, 7, 100; 4.32, 6, 1 1; 3.60, 10 002; 3.41, 9, 1 0; 3.30, 5, 02 ; 3.00, 5, 111; 2.80, 7, 12 ; 2.07, 6, 211/21 /1 3; 1.778, 5, 3 /2 3. Chenite forms minute, singly terminated, transparent to translucent sky-blue crystals from 0.1 to over 1 mm long, elongated approximately [032]. Twenty different forms (pinacoids) have been identified on the four crystals studied. A good cleavage on {100}, and traces of a second on {001}, can be observed. Optically, chenite is biaxial negative, 2 V(measured) = 67±1°, 2 V(calc.) = 68° (Na). The refractive indices are α 1.871±0.005, β 1.909±0.005, γ 1.927±0.005 (Na). Dispersion is strong, r≫v. The mineral is weakly pleochroic. H (Mohs) ∼ 2½. D = 5.98, and calculated D x = 6.044 g cm −3 .
    Type of Medium: Online Resource
    ISSN: 0026-461X , 1471-8022
    RVK:
    Language: English
    Publisher: Mineralogical Society
    Publication Date: 1986
    detail.hit.zdb_id: 2034522-7
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  • 8
    Online Resource
    Online Resource
    Mineralogical Society ; 2004
    In:  Mineralogical Magazine Vol. 68, No. 3 ( 2004-06), p. 527-539
    In: Mineralogical Magazine, Mineralogical Society, Vol. 68, No. 3 ( 2004-06), p. 527-539
    Abstract: One in four of the Cu-filled cation sites in clinoatacamite, the monoclinic polymorph of atacamite and botallackite, is angle- rather than Jahn-Teller-distorted. Experiments show that this site alone is susceptible to substitution by a non-Jahn-Teller distorting cation of suitable radius and charge, such as Zn 2+ , and also Ni 2+ , Co 2+ , Fe 2+ , Cd 2+ and Mg 2+ . The crystal symmetry changes to rhombohedral when ∼⅓ of the Cu in this site is substituted by e.g. Zn, thus giving paratacamite; the Zn is essential for stability and forms, with larger proportions of Zn, a series to the end-member in which the site is fully occupied by Zn. This end-member, rhombohedral stoichiometric Cu 3 Zn(OH) 6 Cl 2 , has been characterized using natural specimens from Chile and Iran and is named herbertsmithite. The other cations mentioned behave similarly, producing stabilized rhombohedral paratacamites and end-members analogous to herbertsmithite, which if found in nature, as the Ni analogue has been, should be named species. Clinoatacamite, paratacamite and herbertsmithite have rather similar X-ray powder diffraction patterns, but are readily distinguished by infrared spectroscopy. Zn-stabilized paratacamite forms blue-green crystals of rhombohedral habit, with vitreous lustre, e = 1.828-1.830, o = 1.835, uniaxial negative, weakly pleochroic O 〉 E, density: 3.75 g cm -3 , Mohs hardness: 3-3½; space group R , a = 13.654(5), c = 14.041(6) Å, Z = 24, with pronounced R m substructure; six strongest XRD lines 5.452 (100), 2.895 (20), 2.760 (74), 2.262 (52), 1.817 (18), 1.708 (21). Herbertsmithite forms dark green crystals of rhombohedral habit, with vitreous lustre, e = 1.817, o = 1.825, uniaxial negative, weakly pleochroic O 〉 E, density: 3.95 g cm -3 , Mohs hardness: 3-3½;; space group R m with no superstructure observed, a = 6.834(1), c = 14.075(2) Å, Z = 3; six strongest XRD lines 5.466 (55), 4.702 (14), 2.764 (100), 2.266 (36), 1.820 (13), 1.709 (18).
    Type of Medium: Online Resource
    ISSN: 0026-461X , 1471-8022
    RVK:
    Language: English
    Publisher: Mineralogical Society
    Publication Date: 2004
    detail.hit.zdb_id: 2034522-7
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  • 9
    Online Resource
    Online Resource
    Mineralogical Society ; 1989
    In:  Mineralogical Magazine Vol. 53, No. 373 ( 1989-12), p. 583-589
    In: Mineralogical Magazine, Mineralogical Society, Vol. 53, No. 373 ( 1989-12), p. 583-589
    Abstract: Yellow blades on joint surfaces in granite from Merrivale quarry, Dartmoor, Devon, are shown to be of a slightly aresenatian variety of phurcalite by X-ray powder diffraction, infrared spectroscopy, electron microprobe and thermal analyses and optical methods. The results from these techniques are tabulated, including assignments for infrared absorption bands. Comparison of X-ray powder diffraction, infrared spectroscopic and optical data with those obtained from samples of ‘nisaite’, an incompletely described mineral from Nisa, Portugal, indicates that the latter is also phurcalite.
    Type of Medium: Online Resource
    ISSN: 0026-461X , 1471-8022
    RVK:
    Language: English
    Publisher: Mineralogical Society
    Publication Date: 1989
    detail.hit.zdb_id: 2034522-7
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  • 10
    Online Resource
    Online Resource
    Royal Society of Chemistry (RSC) ; 1967
    In:  Journal of the Chemical Society B: Physical Organic ( 1967), p. 1113-
    In: Journal of the Chemical Society B: Physical Organic, Royal Society of Chemistry (RSC), ( 1967), p. 1113-
    Type of Medium: Online Resource
    ISSN: 0045-6470
    Language: English
    Publisher: Royal Society of Chemistry (RSC)
    Publication Date: 1967
    detail.hit.zdb_id: 2194432-5
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