scholarly journals Direct determination of layer packing for a phospholipid solid solution at 0.32-nm resolution.

1994 ◽  
Vol 91 (11) ◽  
pp. 4920-4924 ◽  
Author(s):  
D. L. Dorset
1987 ◽  
Vol 42 (6) ◽  
pp. 746-749 ◽  
Author(s):  
Jenő Juhász ◽  
Sarolta Igaz ◽  
Béla Jóvér ◽  
Zoltán G. Szabó

Abstract Defect Sites of CdO, Reducibility, Analysis Three procedures of chemical analysis are proposed for the direct determination of excess Cd in CdO: a spectrophotometric, a titrimetric and a gravimetric one, for 0-1500 ppm, 500-50,000 ppm and above 5%, respectively. The good reproducibility and reliability is illustrated by results referring to CdO samples heat-treated in H 2 and in air between 100 and 350 °C. Reduction in H2 increases the concentration of excess Cd up to 4000 ppm, above that separate Cd phase forms. The excess Cd in solid solution (interstitial sites) is more resistant against re-oxidation, than the bulk Cd phase.


1998 ◽  
Vol 62 (1) ◽  
pp. 93-111 ◽  
Author(s):  
Eugene E. Foord ◽  
Joseph E. Taggart

AbstractThe turquoise group has the general formula:A0–1B6(PO4)4−x(PO3OH)x(OH)8.4H2O, wherex= 0–2, and consists of six members: planerite, turquoise, faustite, aheylite, chalcosiderite and an unnamed Fe2+-Fe3+analogue. The existence of ‘coeruleolactite’ is doubtful. Planerite is revalidated as a species and is characterized by a dominantA-site vacancy. Aheylite is established as a new member of the group, and is characterized by having Fe2+dominant in theA-site.Chemical analyses of 15 pure samples of microcrystalline planerite, turquoise, and aheylite show that a maximum of two of the (PO4) groups are protonated (PO3OH) in planerite. Complete solid solution exists between planerite and turquoise. Other members of the group show variableA-site vacancy as well. Most samples of ‘turquoise’ are cation-deficient or are planerite. Direct determination of water indicates that there are 4 molecules of water.Planerite, ideally ☐Al6(PO4)2(PO3OH)2(OH)8.4H2O, is white, pale blue or pale green, and occurs as mamillary, botryoidal crusts as much as several mm thick; may also be massive; microcrystalline, crystals typically 2–4 micrometres, luster chalky to earthy, H. 5, somewhat brittle, no cleavage observed, splintery fracture, Dm2.68(2), Dc2.71, not magnetic, not fluorescent, mean RI about 1.60.a7.505(2),b9.723(3),c7.814(2) Å, α 111.43°, β 115.56°, γ 68.69°, V 464.2(1) Å3, Z = 1.Aheylite, ideally Fe2+Al6(PO4)4(OH)8.4H2O, is pale blue or green, and occurs as isolated and aggregate clumps of hemispherical or spherical, radiating to interlocked masses of crystals that average 3 micrometres in maximum dimension; porcelaneous-subvitreous luster, moderate to brittle tenacity, no cleavage observed, hackly to splintery fracture, not magnetic, not fluorescent, biax. (+), mean RI is about 1.63, Dm2.84(2), Dc2.90.a7.400(1),b9.896(1),c7.627(1) Å, α 110.87°, β 115.00°, γ 69.96°, V 460.62(9) Å3, Z = 1.


1961 ◽  
Vol 41 (4) ◽  
pp. 380-384 ◽  
Author(s):  
Arthur F. Dratz ◽  
James C. Coberly
Keyword(s):  

2002 ◽  
Vol 721 ◽  
Author(s):  
Monica Sorescu

AbstractWe propose a two-lattice method for direct determination of the recoilless fraction using a single room-temperature transmission Mössbauer measurement. The method is first demonstrated for the case of iron and metallic glass two-foil system and is next generalized for the case of physical mixtures of two powders. We further apply this method to determine the recoilless fraction of hematite and magnetite particles. Finally, we provide direct measurement of the recoilless fraction in nanohematite and nanomagnetite with an average particle size of 19 nm.


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