Synthesis and Characterization of Cobalt apatite totally and half substituted by Microwave Irradiation. Antibacterial activity

The present paper investigates the preparation of hydroxyapatite and Cobalt (Co) apatite totally and half substituted through a chemical synthesis process. The synthesized powders were characterized by the following analytical techniques: X-ray diffraction (XRD), FT-IR and Scanning electron microscopy (SEM). We have successfully prepared nano-Hap particles with various shapes by controlling pH and preparation temperature in the precipitation method. The HAp prepared in various conditions. It illustrates that the pH value, preparation temperature and component ratio play an important role in controlling the shape of the synthesized particles. It is interesting that those parameters have insignificant effect on size of the particles. The peak profiles of the XRD patterns may indicate that the crystallinity of the particles varies with the pH value and temperature. For examples, the particles prepared over the pH-9 solution at 60°C have high crystallinity than the particles prepared below pH- 9 solution. XRD analyses results showed that the crystallinity increase with increase the component ratio of cobalt. The antibacterial activity of these complexes against Gram positive and Gram negative has also been studied.Keywords: Hydroxyapatite; Cobalt. FTIR spectroscopy, X-ray diffraction(XRD), Scanning electron microscopy (SEM)

Genesis and petrology of Late Neoproterozoic pegmatites and aplites associated with the Taba metamorphic complex in southern Sinai, Egypt

We present new field, petrographical, mineralogical and geochemical data from late Neoproterozoic pegmatites and aplites in southern Sinai, Egypt, at the northernmost limit of the Arabian-Nubian Shield. The pegmatites cross-cut host rocks in the Taba Metamorphic Complex (TMC) with sharp contacts and are divided into massive and zoned pegmatites. Massive pegmatites are the most common and form veins, dykes and masses of variable dimensions; strikes range mainly from E-W through NW-SE to N-S. Mineralogically, the massive pegmatites are divided into K-feldspar-rich and albite-rich groups. Zoned pegmatites occur as lenses of variable dimensions, featuring a quartz core, an intermediate zone rich in K-feldspars and an outer finer-grained zone rich in albite. All compositions are highly evolved and display geochemical characteristics of post-collisional A-type granites: high SiO2, Na2O+K2O, FeO*/MgO, Ga/Al, Zr, Nb, Ga and Y alongside low CaO, MgO, Ba and Sr. They are rich in Rare Earth Elements (REE) and have extreme negative Eu anomalies (Eu/Eu*= 0.03-0.09). A genetic linkage between the pegmatites, aplites and alkali granite is confirmed by their common mild alkaline affinity and many other geochemical characteristics. These pegmatites and aplites represent the last small fraction of liquid remaining after extensive crystallization of granitic magma, injected along the foliation and into fractures of the host metamorphic rocks. The extensional tectonic regime and shallow depth of emplacement are consistent with a post-collisional environment

Petrogenesis of gold-bearing listvenites from the carbonatized mantle section of the Neoproterozoic Ess ophiolite, Western Arabian Shield, Saudi Arabia

The variably serpentinized mantle peridotites of the Late Neoproterozoic Ess ophiolite (Western Saudi Arabia) are highly altered along shear zones and thrust planes to form erosion-resistant listvenites. The listvenites are distinguished petrographically and geochemically into three types: carbonate, silica-carbonate and silica (birbirite) listvenites. Geochemical analyses are consistent with expectations from petrography: carbonate listvenite is low in SiO₂ content but high in MgO, Fe₂O₃, and CaO relative to silica-carbonate and birbirite, which is remarkably high in SiO₂ at the expense of all other components. The total REE contents are low in silica-carbonate and carbonate listvenites but highly enriched in birbirite, with a large positive Eu anomaly. The host serpentinites have all the characteristics typically associated with highly depleted mantle harzburgite protoliths in supra-subduction fore-arc settings: bulk compositions are low in Al₂O₃ and CaO with high Mg# [molar Mg/(Mg + Fe)], relict Cr-spinel has high Cr# [molar Cr/(Cr + Al)] and low TiO₂, and relict olivine has high Mg# and NiO content. The Cr-spinel relics are also found in the listvenites; those in serpentinite and carbonate listvenites have significantly higher Mg# than those in silica-carbonate and birbirite, suggesting re-equilibration of Cr-spinel in the later phases of listvenitization. The varieties of listvenite capture successive stages of fluid-mediated replacement reactions. The carbonate listvenite appears to have developed syn-contemporaneously with serpentinization, whereas silica-carbonate listvenite and birbirite formed later. The listvenite formation resulted in leaching and removal of some components accompanied by deposition of others in the solid products, notably CO₃, SiO₂, REE (especially Eu), Au, Zn, As, Sb and K. Our data show that listvenitization concentrated gold at sub-economic to economic grades; measured gold concentrations in the host serpentinite are 0.5–1.7 ng/g, versus 4–2569 ng/g in carbonate listvenite, 43–3117 ng/g in silica-carbonate listvenite and 5–281 ng/g in birbirite. The listvenite deposits in the Jabal Ess area merit further exploration for gold

The common origin and alteration history of the hypabyssal and volcanic phases of the Wadi Tarr albitite complex, southern Sinai, Egypt

New data and interpretations are presented for the igneous albitites of the Wadi Tarr area, southern Sinai, Egypt. The albitite masses are isolated in outcrop from any granitic intrusions and have intrusive contacts against the country rocks without any structural control. They have marginal zones of breccias with jigsaw-fit angular clasts suggesting explosive, in-situ formation. The albitites are of two types: the western, medium-grained, hypabyssal albitite and the eastern, fine-grained porphyritic albitite. The field relations suggest emplacement at different levels in a magmatic cupola: the hypabyssal texture and steeply dipping slope of the upper contact of the western albitite imply deeper emplacement whereas the gently dipping contacts and porphyritic texture of the eastern albitite masses indicate that they define the probable location of the cupola apex. Both types of albitites consist of albite (92–97%) with minor amounts of quartz, K-feldspar and biotite. The accessory minerals include Fe-oxides, augite, sulphides, zircon, rutile, xenotime, titanite, allanite and monazite. The whole-rock compositions of the hypabyssal and porphyritic albitites are closely related, but the porphyritic type has lower abundances of Sr, Ba, Y, Nb, Th and Zr. We show that the hypabyssal and porphyritic albitites have a common petrogenetic origin, most likely as late-stage cumulates from a fractionating, strongly alkaline A-type magma, consistent with the compositions of the mafic minerals. The source magma was probably a tephritic liquid; we use MELTS models to show that only a sufficiently alkaline magma follows a differentiation path that both avoids quartz saturation and encounters the alkali feldspar solvus, reaching a residual liquid in equilibrium with highly sodic feldspar. Although the MELTS results show a chemically consistent means of forming igneous albitite, they are incomplete in that physical segregation mechanisms are still required to isolate the albite from mafic minerals and or a low-temperature aqueous alteration stage is needed to leach K from the feldspar. Alteration surrounding the Wadi Tarr albitites is extensive and dominated by alkali metasomatism similar to fenitization. Alteration in the marginal breccia zone of the albitite is dominated by precipitation of amphibole and carbonate in veins and in the breccia matrix, whereas the volcanic country rocks show replacement of feldspars by sericite, carbonate and epidote as well as vein carbonate. The altered volcanic country rocks show lower concentrations of Fe_2O_3, Sr, Cu, Pb, Ba and Ce, accompanied by higher concentrations of Na2O and MgO compared to unaltered equivalent samples

Petrogenesis of gold-bearing listvenites from the carbonatized mantle section of the Neoproterozoic Ess ophiolite, Western Arabian Shield, Saudi Arabia

The variably serpentinized mantle peridotites of the Late Neoproterozoic Ess ophiolite (Western Saudi Arabia) are highly altered along shear zones and thrust planes to form erosion-resistant listvenites. The listvenites are distinguished petrographically and geochemically into three types: carbonate, silica-carbonate and silica (birbirite) listvenites. Geochemical analyses are consistent with expectations from petrography: carbonate listvenite is low in SiO₂ content but high in MgO, Fe₂O₃, and CaO relative to silica-carbonate and birbirite, which is remarkably high in SiO₂ at the expense of all other components. The total REE contents are low in silica-carbonate and carbonate listvenites but highly enriched in birbirite, with a large positive Eu anomaly. The host serpentinites have all the characteristics typically associated with highly depleted mantle harzburgite protoliths in supra-subduction fore-arc settings: bulk compositions are low in Al₂O₃ and CaO with high Mg# [molar Mg/(Mg + Fe)], relict Cr-spinel has high Cr# [molar Cr/(Cr + Al)] and low TiO₂, and relict olivine has high Mg# and NiO content. The Cr-spinel relics are also found in the listvenites; those in serpentinite and carbonate listvenites have significantly higher Mg# than those in silica-carbonate and birbirite, suggesting re-equilibration of Cr-spinel in the later phases of listvenitization. The varieties of listvenite capture successive stages of fluid-mediated replacement reactions. The carbonate listvenite appears to have developed syn-contemporaneously with serpentinization, whereas silica-carbonate listvenite and birbirite formed later. The listvenite formation resulted in leaching and removal of some components accompanied by deposition of others in the solid products, notably CO₃, SiO₂, REE (especially Eu), Au, Zn, As, Sb and K. Our data show that listvenitization concentrated gold at sub-economic to economic grades; measured gold concentrations in the host serpentinite are 0.5–1.7 ng/g, versus 4–2569 ng/g in carbonate listvenite, 43–3117 ng/g in silica-carbonate listvenite and 5–281 ng/g in birbirite. The listvenite deposits in the Jabal Ess area merit further exploration for gold

Petrological Characteristics of the Bou-azzer Ophiolote, Anti-atlas, Morocco : Nature of Proterozoic Oceanic Lithosphere

金沢大学大学院自然科学研究科Promoting Environmental Pesearch in Pan-Japan Sea Area : Young Researchers\u27 Network, Schedule: March 8-10,2006,Kanazawa Excel Hotel Tokyu, Japan, Organized by: Kanazawa University 21st-Century COE Program, Environmental Monitoring and Prediction of Long- & Short- Term Dynamics of Pan-Japan Sea Area ; IICRC(Ishikawa International Cooperation Research Centre), Sponsors : Japan Sea Research ; UNU-IAS(United Nations University Institute of Advanced Studies)+Ishikawa Prefecture Government ; City of Kanazaw

Influence of Nanosilver Synthesis Conditions on its Architecture

Silver nitrate reduction in presence of Ethylene glycol (EG) and Poly Ethylene glycol (PEG) represents one from the simplest techniques for silver nano-powder fabrication. Where EG act as reducing agent and PEG act as stabilizing agent. The impact of presence either the reducing agent or the stabilizing agent at the reaction media on the properties ofsynthesized silver were recorded. Regarding to the chain length of PEG was discovered to play the key role in the formation of nano-silver. Accordingly, the variation in the stabilizing agent (PEG) molecular weight on the morphological structures of produced silver was recorded. The formation of nano-silver was confirmed using UV–Vis spectroscopy. The UV– visiblescanning results for the aqueous reaction medium containing silver ion has been demonstrated characteristics peak at 420nm that corresponding to the plasmon absorbance of silver nanoparticle. X-ray diffraction (XRD) was utilized to determine the crystalline structure of the prepared silver nano-powders.The crystalline structure of prepared nano-silver was producein hexagonal, cubic crystal and face centered cubic configurations with different plane of orientation. Scanning electron micrographs of synthesized silver indicated that nano-silver were prepared in morphological structures as nano-particle.Keywords: Silver, Nano-structures, Nano-material, Reduction, Characterization

Influence of Nanosilver Synthesis Conditions on its Architecture

Silver nitrate reduction in presence of Ethylene glycol (EG) and Polyethylene glycol (PEG) represents one from the simplest techniques for silver nano-powder fabrication. Where EG act as reducing agent and PEG act as stabilizing agent. The impact of presence either the reducing agent or the stabilizing agent at the reaction media on the properties of synthesized silver were recorded. Regarding to the chain length of PEG was discovered to play the key role in the formation of nano-silver. Accordingly, the variation in the stabilizing agent (PEG) molecular weight on the morphological structures of produced silver was recorded. The formation of nano-silver was confirmed using UV–Vis spectroscopy. The UV–visible scanning results for the aqueous reaction medium containing silver ion has been demonstrated characteristics peak at 420nm that corresponding to the plasmon absorbance of silver nanoparticle. X-ray diffraction (XRD) was utilized to determine the crystalline structure of the prepared silver nano-powders. The crystalline structure of prepared nano-silver was produced in hexagonal, cubic crystal and face centered cubic configurations with different plane of orientation. Scanning electron micrographs of synthesized silver indicated that nano-silver were prepared in morphological structures as nanoparticle

Genesis of peculiarly zoned Co, Zn and Mn-rich chromian spinel in serpentinite of Bou-Azzer ophiolite, Anti-Atlas, Morocco

金沢大学大学院自然科学研究科自然計測The peculiar Co, Zn and Mn-rich chromian spinels are hosted by magnetite veins, serpentinites and chromitites of the mantle section of the Proterozoic Bou-Azzer ophiolite, Morocco. The spinel is complexly zoned either optically or chemically, and exhibits anomalously high MnO, ZnO and CoO contents (up to 22, 7.5 and 2 wt%, respectively). It has four distinct optical zones particularly in the magnetite veins and less typically in serpentinites. The highest level of these elements, probably divalent, is recorded within the ferritchromite zone and/or within the core zone if the ferritchromite zone is absent. These elements as well as Fe exhibit enrichment along grain boundaries and fractures of the altered spinels. Fe, Mn, Zn and Co were most probably supplied from olivine upon severe serpentinization during and after obduction of the ophiolite. The enrichment of the Bou-Azzer chromian spinel in Mn, Zn and Co was governed mainly by the fluid/mineral (spinel) ratio and partition coefficient between spinel and the relevant fluid among many factors. The Co-, Zn- and Mn-rich chromian spinels can be used as an exploration guide for Co-Ni-Zn-Cu sulfide mineralization associated with serpentinized peridotites

Late Neoproterozoic layered mafic intrusion of arc-affinity in the Arabian-Nubian Shield : a case study from the Shahira layered mafic intrusion, southern Sinai, Egypt

The Shahira Layered Mafic Intrusion (SLMI), which belongs to the late Neoproterozoic plutonic rocks of the Arabian-Nubian Shield, is the largest layered mafic intrusion in southern Sinai. Field relations indicate that it is younger than the surrounding metamorphic rocks and older han the post-orogenic granites. Based on variation in mineral paragenesis and chemical composition, the SLMI is distinguished into pyroxene-hornblende gabbro, hornblende gabbro and diorite lithologies. The outer zone of the mafic intrusion is characterized by fine-grained rocks (chilled margin gabbroic facies), with typical subophitic and/or microgranular textures. ifferent rock units from the mafic intrusion show gradational boundaries in between. They show some indications of low grade metamorphism, where primary minerals are transformed into secondary ones. Geochemically, the Shahira layered mafic intrusion is characterized by enrichment in LILE relative to HFSE (e.g. Nb, P, Zr, Ti, Y), and LREE relative to HREE [(La/Lu)n= 4.75-8.58], with subalkaline characters. It has geochemical characteristics of pre-collisional arc-type environment. The geochemical signature of the investigated gabbros indicates partial melting of mantle wedge in a volcanic-arc setting, being followed by fractional crystallization and crustal contamination. Fractional crystallization processes played a vital role during emplacement of the Shahira intrusion and evolution of its mafic and intermediate rock units. The initial magma was evolved through crystallization of ornblende which was caused by slight increasing of H2O in the magma after crystallization of iquidus olivine, pyroxene and Ca-rich plagioclase. The gabbroic rocks crystallized at pressures between 4.5 and 6.9kbar (~15-20km depth). Whereas, the diorites yielded the lowest crystallization pressure between 1.0 to 4.4Kbar (<10km depth). Temperature was estimated by several eothermometers, which yielded crystallization temperatures ranging from 835º to 958ºC for the gabbros, and from 665º to 862ºC for the diorites. Field, petrological, geochemical and mineralogical characteristics of the SLMI are akin to the Egyptian layered mafic-ultramafic ntrusions of volcanic-arc setting, not ophiolitic rock