Search results for "Crystallization"

Chronology of early Archaean granite-greenstone evolution in the Barberton Mountain Land, South Africa, based on precise dating by single zircon evap…

1991

We report precise 207Pb/206Pb single zircon evaporation ages for low-grade felsic metavolcanic rocks within the Onverwacht and Fig Tree Groups of the Barberton Greenstone Belt (BGB), South Africa, and from granitoid plutons bordering the belt. Dacitic tuffs of the Hooggenoeg Formation in the upper part of the Onverwacht Group yield ages between 3445 +/- 3 and 3416 +/- 5 Ma and contain older crustal components represented by a 3504 +/- 4 Ma old zircon xenocryst. Fig Tree dacitic tuffs and agglomerates have euhedral zircons between 3259 +/- 5 and 3225 +/- 3 Ma in age which we interpret to reflect the time of crystallization. A surprisingly complex xenocryst population in one sample documents …

Evidences of magma mixing in the "Daly gap" of the alkaline suites: a case study from the enclaves of Pantelleria (Italy)

2006

The island of Pantelleria consists of trachytes, pantellerites and minor mildly alkaline basalts. Rocks of intermediate composition (falling in the so-called ‘Daly Gap’) such as mugearites, benmoreites and mafic trachytes occur only in the form of enclaves in trachytes and pantellerites inside the main caldera of the island (Caldera ‘Cinque Denti’), which collapsed during the ‘Green Tuff ’ ignimbrite eruption at 50 ka. The enclaves include volcanic, subvolcanic and intrusive rock types. The enclaves in host trachyte contain traces of glass; devitrified glass occurs within enclaves in host pantellerites. Minerals in the enclaves show regular compositional variations with whole-rock silica co…

Animations of dynamic recrystallization with the numerical modelling system Elle

2001

VIEPS/Mainz Microstructure Course

2000

Investigation of the Na2O/Ag2O ratio on the synthesis conditions and properties of the 80TeO2–10ZnO–[(10−x)Na2O–xAg2O] glasses

2019

International audience; Properties of the tellurite glasses 80TeO2–10ZnO–[(10−x)Na2O–xAg2O] are investigated as a function of the substitution ratio x between Na2O and Ag2O. One observe that the variation of glass transition temperature decreases monotonously with x and that surface crystallization mechanism is favored. The assignment of the Raman bands and their relation with the underlying glass structure is discussed. While both Na2O and Ag2O oxides act as glass network modifiers, their progressive equimolar substitution does not lead to a meaningful evolution in the structure of the TZ[Na10-xAgx] glass. The refractive index and the cut-off wavelength are found to increase with x. The co…

Ni-containing spinel aluminates glass-ceramic materials obtained from cordieritic bulk glasses

2003

Monolithic glasses with compositions 2MO � 2Al2O3 � 5SiO2, being M ¼ Ni and equimolar mixtures of Ni and Mg, were prepared at 1650 C by melting mixtures of raw materials. The crystallization of monoliths was produced by heattreatment at several temperatures up to 1200 C. The crystallization sequence was followed by differential thermal analysis (DTA), X-ray powder diffraction (XRD), field emission scanning electron microscopy (FESEM) and energy dispersive X-ray (EDX) and diffuse reflectance spectroscopies. Surprisingly, the only crystalline phase formed after heating up to 1100 C was a nickel-containing aluminate spinel for both compositions. The microstructural characterization indicated t…

Effect of some additives on the development of spinel-based glass-ceramic glazes for floor-tiles

2005

Abstract The feasibility of developing spinel-based glass-ceramic glazes from a glass with composition in the system ZnO–MgO–B 2 O 3 –Al 2 O 3 –SiO 2 was examined. To do it additional fluxes and/or nucleants were added to a parent glass before melting. Pressed pellets of powdered glasses were submitted to standard thermal treatments up to 1200 °C. The crystallization path and the microstructural development at several temperatures were followed by several experimental techniques. The results showed that additions of TiO 2 as nucleant or additional B 2 O 3 as flux to the chosen glass favored the crystallization of cordierite or mullite as main crystalline phase. Glasses which also contained …

Hybrid Organic-Inorganic Nanostructures Fabricated from Layer-by-Layer Self-Assembled Multilayers of Hyperbranched Polyglycerols and Phosphorus Dendr…

2007

Multilayer thin films of cationic phosphorous dendrimers and anionic hyperbranched polyglycerols were fabricated by electrostatic layer-by-layer (LbL) self-assembly (SA). The film formation was monitored by surface plasmon resonance (SPR) spectroscopy and UV-visible spectroscopy, and it was found that the stepwise, alternating deposition results in a linear growth up to four bilayers. Hybrid organic-TiO2 nanostructures were generated by exposing the supramolecular multilayers to TiCl4 precursors. The amounts of TiO2 incorporated inside the scaffolds could be tuned by controlling the porosity of the multilayers with the addition of a small amount of salts. The resulting hybrid films exhibit …

Controlled Crystallization of CaCO3on Hyperbranched Polyglycerol Adsorbed to Self-Assembled Monolayers

2005

The formation of biominerals by living organisms is governed by the cooperation of soluble and insoluble macromolecules with peculiar interfacial properties. To date, most of the studies on mineralization processes involve model systems that only account for the existence of one organic matrix and thus disregard the interaction between the soluble and insoluble organic components that is crucial for a better understanding of the processes taking place at the inorganic-organic interface. We have set up a model system composed of a matrix surface, namely, a self-assembled monolayer (SAM), and a soluble component, hyperbranched polyglycerol. The model mineral calcium carbonate displays diverse…

Glycosylamines of 4,6-O-butylidene-α-d-glucopyranose: synthesis and characterization of glycosylamines, and the crystal structure of 4,6-O-butylidene…

2002

A total of nine glycosylamines of 4,6-O-butylidene-α-D-glucopyranose were synthesized using primary amines having various groups in their ortho- or para-positions. Among these, six are monoglycosylamines, including one primary glycosylamine, and three are bis-glycosylamines. All these compounds were characterized by 1H, 1H–1H COSY, 1H–13C COSY and 13C NMR spectroscopy and FTIR spectra. The FAB mass spectra provided the molecular weights of the products by exhibiting the corresponding molecular ion peaks. The crystal structure of 4,6-O-butylidene-N-(o-chlorophenyl)-β-D-glucopyranosylamine revealed the C-1 glycosylation, the β-anomeric nature, and the 4C1 chair conformation of the saccharide …