Molecular Hydrogen in Natural Mayenite

In the last 15 years, zeolite-like mayenite, Ca12Al14O33, has attracted significant attention in material science for its variety of potential applications and for its simple composition. Hydrogen plays a key role in processes of electride material synthesis from pristine mayenite: {Ca12Al14O32}2+(O2)!{Ca12Al14O32}2+(e)2. Apresence of molecular hydrogen in synthetic mayenite was not confirmed by the direct methods. Spectroscopy investigations of mayenite group mineral fluorkyuygenite, with empirical formula (Ca12.09Na0.03)P 12.12(Al13.67Si0.12Fe3+ 0.07Ti4+ 0.01)P 12.87O31.96 [F2.02Cl0.02(H2O)3.22(H2S)0.15 0.59]P 6.00, show the presence of an unusual band at 4038 cm1, registered for the first time and related to molecular hydrogen, apart from usual bands responding to vibrations of mayenite framework. The band at 4038 cm1 corresponding to stretching vibrations of H2 is at lower frequencies in comparison with positions of analogous bands of gaseous H2 (4156 cm1) and H2 adsorbed at active cation sites of zeolites (4050–4100 cm1). This points out relatively strong linking of molecular hydrogen with the fluorkyuygenite framework. An appearance ofH2 in the fluorkyuyginite with ideal formula Ca12Al14O32[(H2O)4F2], which formed after fluormayenite, Ca12Al14O32[ 4F2], is connected with its genesis. Fluorkyuygenite was detected in gehlenite fragments within brecciaed pyrometamorphic rock (Hatrurim Basin, Negev Desert, Israel), which contains reduced mineral assemblage of the Fe-P-C system (native iron, schreibersite, barringerite, murashkoite, and cohenite). The origin of phosphide-bearing associations is connected with the e ect of highly reduced gases on earlier formed pyrometamorphic rocks

New Mineral with Modular Structure Derived from Hatrurite from the Pyrometamorphic Rocks of the Hatrurim Complex: Ariegilatite, BaCa12(SiO4)4(PO4)2F2O, from Negev Desert, Israel

Ariegilatite, BaCa12(SiO4)4(PO4)2F2O (R3m, a = 7.1551(6) Å, c = 41.303(3) Å, V = 1831.2(3) Å3, Z = 3), is a new member of the nabimusaite group exhibiting a modular intercalated antiperovskite structure derived from hatrurite. It was found in a few outcrops of pyrometamorphic rocks of the Hatrurim Complex located in the territories of Israel, Palestine and Jordan. The holotype specimen is an altered spurrite marble from the Negev Desert near Arad city, Israel. Ariegilatite is associated with spurrite, calcite, brownmillerite, shulamitite, CO3-bearing fluorapatite, fluormayenite-fluorkyuygenite and a potentially new mineral, Ba2Ca18(SiO4)6(PO4)3(CO3)F3O. Ariegilatite is overgrown and partially replaced by stracherite, BaCa6(SiO4)2[(PO4)(CO3)]F. The mineral forms flat disc-shaped crystals up to 0.5 mm in size. It is colorless, transparent, with white steaks and vitreous luster. Optically, ariegilatite is uniaxial, negative: ! = 1.650(2), " = 1.647(2) ( = 589 nm). The mean composition of the holotype ariegilatite, (Ba0.98K0.01Na0.01)S1(Ca11.77Na0.08Fe2+ 0.06Mn2+ 0.05Mg0.04)S12(Si3.95Al0.03Ti0.02)S4(P1.70C0.16Si0.10S6+ 0.03 V0.01)S2F2.04O0.96, is close to the end-member formula. The structure of ariegilatite is described as a stacking of the two modules {F2OCa12(SiO4)4}4+ and {Ba(PO4)2}4 along (001). Ariegilatite, as well as associated stracherite, are high-temperature alteration products of minerals of an early clinker-like association. These alterations took place under the influence of pyrometamorphism by-products, such as gases and fluids generated by closely-spaced combustion foci

International and russian experience in monitoring maternal near-miss cases

Maternal mortality continues to be an important population indicator that characterizes the level of development of the obstetric and gynecological service, as well as the entire healthcare system. World Health Organization (WHO) recommends to pay more attention to the analysis of obstetric near-miss cases in developed countries with low maternal mortality. The review presents methodological frameworks for WHO near-miss case management, as well as features of registration of such cases in Brazil, the United States of America, New Zealand, Canada, Europe, China and the Russian Federation. There is a system created in the Russian Federation that has the following main differences: 1) real-time coverage of life-threatening obstetric events in the whole country and all medical organizations; 2) registration of life-threatening obstetric events and maternal deaths in unified system; 3) all-day monitoring performed by the largest national obstetric and gynecological institution; 4) the possibility of consulting patients in life-threatening obstetric emergencies by the leading specialists of the country in obstetrics, gynecology and anesthesiology using telemedicine technologies. Conclusion. A unique system of recording and monitoring life-threatening obstetric conditions has been developed in the Russian Federation

New Mineral with Modular Structure Derived from Hatrurite from the Pyrometamorphic Rocks of the Hatrurim Complex: Ariegilatite, BaCa12(SiO4)4(PO4)2F2O, from Negev Desert, Israel

Ariegilatite, BaCa12(SiO4)4(PO4)2F2O (R 3 ¯ m, a = 7.1551(6) Å, c = 41.303(3) Å, V = 1831.2(3) Å3, Z = 3), is a new member of the nabimusaite group exhibiting a modular intercalated antiperovskite structure derived from hatrurite. It was found in a few outcrops of pyrometamorphic rocks of the Hatrurim Complex located in the territories of Israel, Palestine and Jordan. The holotype specimen is an altered spurrite marble from the Negev Desert near Arad city, Israel. Ariegilatite is associated with spurrite, calcite, brownmillerite, shulamitite, CO3-bearing fluorapatite, fluormayenite-fluorkyuygenite and a potentially new mineral, Ba2Ca18(SiO4)6(PO4)3(CO3)F3O. Ariegilatite is overgrown and partially replaced by stracherite, BaCa6(SiO4)2[(PO4)(CO3)]F. The mineral forms flat disc-shaped crystals up to 0.5 mm in size. It is colorless, transparent, with white steaks and vitreous luster. Optically, ariegilatite is uniaxial, negative: ω = 1.650(2), ε = 1.647(2) (λ = 589 nm). The mean composition of the holotype ariegilatite, (Ba0.98K0.01Na0.01)Σ1(Ca11.77Na0.08Fe2+0.06Mn2+0.05Mg0.04)Σ12(Si3.95Al0.03Ti0.02)Σ4(P1.70C0.16Si0.10S6+0.03V0.01)Σ2F2.04O0.96, is close to the end-member formula. The structure of ariegilatite is described as a stacking of the two modules {F2OCa12(SiO4)4}4+ and {Ba(PO4)2}4− along (001). Ariegilatite, as well as associated stracherite, are high-temperature alteration products of minerals of an early clinker-like association. These alterations took place under the influence of pyrometamorphism by-products, such as gases and fluids generated by closely-spaced combustion foci

Crystal Chemistry and Structural Complexity of Natural and Synthetic Uranyl Selenites

Comparison of the natural and synthetic phases allows an overview to be made and even an understanding of the crystal growth processes and mechanisms of the particular crystal structure formation. Thus, in this work, we review the crystal chemistry of the family of uranyl selenite compounds, paying special attention to the pathways of synthesis and topological analysis of the known crystal structures. Comparison of the isotypic natural and synthetic uranyl-bearing compounds suggests that uranyl selenite mineral formation requires heating, which most likely can be attributed to the radioactive decay. Structural complexity studies revealed that the majority of synthetic compounds have the topological symmetry of uranyl selenite building blocks equal to the structural symmetry, which means that the highest symmetry of uranyl complexes is preserved regardless of the interstitial filling of the structures. Whereas the real symmetry of U-Se complexes in the structures of minerals is lower than their topological symmetry, which means that interstitial cations and H2O molecules significantly affect the structural architecture of natural compounds. At the same time, structural complexity parameters for the whole structure are usually higher for the minerals than those for the synthetic compounds of a similar or close organization, which probably indicates the preferred existence of such natural-born architectures. In addition, the reexamination of the crystal structures of two uranyl selenite minerals guilleminite and demesmaekerite is reported. As a result of the single crystal X-ray diffraction analysis of demesmaekerite, Pb2Cu5[(UO2)2(SeO3)6(OH)6](H2O)2, the H atoms positions belonging to the interstitial H2O molecules were assigned. The refinement of the guilleminite crystal structure allowed the determination of an additional site arranged within the void of the interlayer space and occupied by an H2O molecule, which suggests the formula of guilleminite to be written as Ba[(UO2)3(SeO3)2O2](H2O)4 instead of Ba[(UO2)3(SeO3)2O2](H2O)3

Vorlanite, (CaU6+)O4, from Jabel Harmun, Palestinian Autonomy, Israel

Vorlanite (CaU6+)O4 Fm3̄m, a = 5.3647(9) Å, V = 154.40(4) Å3, Z = 2 was found in larnite pyrometamorphic rocks of the Hatrurim formation at the Jabel Harmun locality, Judean Desert, Palestinian Autonomy. Vorlanite crystals from these larnite rocks are dark-gray with greenish hue in transmitted light. This color in transmitted light is in contrast to dark-red vorlanite Fm3̄m, a = 5.3813(2) Å, V = 155.834(10)Å3, Z = 2 from the type locality Upper Chegem caldera, Northern Caucasus. Heating above 750 °C of dark-gray vorlanite from the Jabel Harmun, as well as dark-red vorlanite from Caucasus, led to formation of yellow trigonal uranate CaUO4. The unusual color of vorlanite from Jabel Harmun is assumed to be related to small impurities of tetravalent uranium