scholarly journals Ranciéit a doprovodné minerály z Rychaltic u Frýdku-Místku (Morava, Česká republika)

2021 ◽  
Vol 29 (1) ◽  
pp. 41-48
Author(s):  
Dalibor Matýsek ◽  
Jakub Jirásek ◽  
Aneta Minaříková ◽  
Petr Skupien
Keyword(s):  
Manganese Oxides ◽  
Middle Part ◽  
Published Data ◽  
X Ray Diffraction ◽  
Scattered Electron ◽  
The Czech Republic ◽  
Outer Western Carpathians ◽  
Manganese Minerals ◽  
The One ◽  
Dark Pink

Recently described small outcrop of the upper part of the Barnasiówka Formation yielded several manganese oxidic minerals. Outcrop at the bank of the Krnalovice Stream (GPS N 49°38.623’ E 018°14.630’) consists of Lower Turonian greenish to grey-black laminated claystone alternating with grey chert. The whole sequence is a part of the Baška facies of the Silesian Unit, Outer Western Carpathians. In the middle part of the profile occur concretional aggregates containing manganese minerals. The central pale part of these aggregates is composed of quartz (ca. 90 wt.%), albite (ca. 9 wt.%), and muscovite, the darker rim of quartz (ca. 80 wt.%), goethite (ca. 10 wt.%), illite, todorokite, plagioclase, K-feldspar, and pyrite. Occasionally, remains of Mn-rich siderite were preserved in the cores. We suppose that they are in fact weathering products of carbonate-rich silicites. Manganese oxides also enter fissures in form of thin black coatings. Powder X-ray diffraction proved the presence of todorokite, ranciéite, pyrolusite, and possible vernadite. Todorokite forms black coatings with submetallic lustre, often associating with ranciéite. Ranciéite is dark pink to pinkish-brown, with a metallic lustre. Back-scattered electron images reveal its extremely thin tabular, sometimes undulated crystals and hexagonally oriented intergrowths. Powder diffraction data are strongly affected by preferred orientation, with dominating basal reflections of 001 plane at 7.4849 Å and plane 002 at 3.7424 Å. Its average formula from nine WDS spots (Ca0.14Mg0.01Ba0.01K0.01)Σ0.17(Mn4+0.86Si0.02Al0.03Fe0.01)Σ0.92O2.00·0.88H2O (based on 2 anions, water calculated from the ratio of cation sum / H2O in the formula according to Post et al. 2008) and CaO/MnO2 ratio 9 to 12 correspond well to the published data for this phase. Ranciéite is a rather common phyllomanganate from various geological environments, but this locality represents its first unambiguous occurrence in the Czech Republic. It closely resembles the one from Polish flysch Carpathians from Nowa Wieś near Rzesów.

scholarly journals Phase and chemical composition analysis of pigments used in Cucuteni Neolithic painted ceramics

2007 ◽  
Vol 34 ◽  
pp. 281-288 ◽  
Author(s):  
Bogdan Constantinescu ◽  
Roxana Bugoi ◽  
Emmanuel Pantos ◽  
Dragomir Popovici
Keyword(s):  
Manganese Oxides ◽  
Mineralogical Composition ◽  
Composition Analysis ◽  
X Ray Diffraction ◽  
Trade Routes ◽  
X Ray ◽  
Manganese Minerals ◽  
Chemical Composition Analysis ◽  
Main Components ◽  
Phase And Chemical Composition

Two analytical methods – 241Am-based X-Ray Fluorescence (XRF) and Synchrotron Radiation X-ray Diffraction (SR-XRD) – were used to investigate the elemental and mineralogical composition of pigments which decorate some Cucuteni Neolithic ceramic sherds. Local hematite and local calcite were the main components for red and white pigments, respectively. For black pigments, iron oxides (e.g. magnetite) were used. They were often mixed with manganese oxides (e.g. jacobsite), which originated from Iacobeni manganese minerals deposits on the Bistrita River. Taking into account the results of the experiments, several conclusions regarding manufacturing procedures employed, and potential trade routes during the Neolithic were drawn.

scholarly journals ZnOTe Compounds Grown by DC-Magnetron Co-Sputtering

Coatings ◽  
2021 ◽  
Vol 11 (5) ◽  
pp. 570
Author(s):  
Olga Sánchez ◽  
Manuel Hernández-Vélez
Keyword(s):  
Molar Fraction ◽  
Variable Parameter ◽  
Point Of View ◽  
X Ray Diffraction ◽  
X Ray ◽  
Sample Series ◽  
Solid Phases ◽  
The One ◽  
High Bulk ◽  
Substrate Sample

ZnOTe compounds were grown by DC magnetron cosputtering from pure Tellurium (Te) and Zinc (Zn) cathodes in O2/Ar atmosphere. The applied power on the Zn target was constant equal to 100 W, while the one applied on the Te target took two values, i.e., 5 W and 10 W. Thus, two sample series were obtained in which the variable parameter was the distance from the Te targets to the substrate. Sample compositions were determined by Rutherford Backscattering Spectroscopy (RBS) experiments. Structural analysis was done using X-Ray diffraction (XRD) spectrometry and the growth of the hexagonal w-ZnO phase was identified in the XRD spectra. RBS results showed high bulk homogeneity of the samples forming ZnOTe alloys, with variable Te molar fraction (MF) ranging from 0.48–0.6% and from 1.9–3.1% for the sample series obtained at 5 W and 10 W, respectively. The results reflect great differences between the two sample series, particularly from the structural and optical point of view. These experiments point to the possibility of Te doping ZnO with the permanence of intrinsic defects, as well as the possibility of the formation of other Te solid phases when its content increases. The results and appreciable variations in the band gap transitions were detected from Photoluminescence (PL) measurements.

Effects of Film Interfaces on the Properties of Poly-Si Grown by The Metal-Induced Technique for Solar Cell Applications

2003 ◽  
Vol 796 ◽  
Author(s):  
Chunhai Ji ◽  
Wayne A. Anderson
Keyword(s):  
Seed Layer ◽  
Lattice Mismatch ◽  
Xrd Analysis ◽  
Crystal Defects ◽  
Photon Absorption ◽  
X Ray Diffraction ◽  
Lattice Match ◽  
Silicide Layer ◽  
Layer Sample ◽  
The One

ABSTRACTIn the metal-induced growth (MIG) process, the poly-Si layer hetero-epitaxially grows from a thin silicide layer, formed by reaction of a metal seed-layer and sputtered silicon, due to an extremely close lattice match between silicon and the metal silicide. The produced poly-Si has shown a promising device quality for photovoltaic applications. Recent results show that the interface of the silicide and poly-Si has a significant effect on the properties of the poly-Si which works as an active layer for photon absorption. In the study of the MIG process, two metals were used as a seed-layer, i.e. Ni and Co. Although CoSi2has a larger lattice mismatch with Si (1.2%) than does NiSi2(0.4%), the poly-Si growing from Co has a smoother interface between the poly-Si and silicide, while the one for the Ni seed-layer samples is rather rough. Backscattered XSEM shows that the Ni-contained phase extended into the Si layer by forming long spikes. This might cause crystal defects in the Si layer. The Auger depth profile also showed that the Ni atoms diffuse into the Si layer much more than does the Co. This kind of difference in interface structure causes the different properties of the poly-Si layer. X-ray diffraction (XRD) analysis on the Si layer showed that the Co seed-layer sample had a predominant growth orientation of (220) and the FWHM of 0.2°. The Ni seed-layer samples grew mainly in both <111> and <220> direction, with FWHM of 0.3° and 0.4°, respectively. By comparison, the poly-Si from the Co seed-layer had a higher carrier lifetime of 0.458μs compared to 0.305μs from Ni.

The crystal chemistry of the uranyl carbonate mineral grimselite, (K, Na)3Na[(UO2)(CO3)3](H2O), from Jáchymov, Czech Republic

2012 ◽  
Vol 76 (3) ◽  
pp. 443-453 ◽  
Author(s):  
J. Plášil ◽  
K. Fejfarová ◽  
R. Skála ◽  
R. Škoda ◽  
N. Meisser ◽  
...  
Keyword(s):  
Crystal Structure ◽  
Czech Republic ◽  
Structure Refinement ◽  
Unit Cell ◽  
Carbonate Mineral ◽  
X Ray Diffraction ◽  
The Czech Republic ◽  
Cell Parameters ◽  
Uranyl Carbonate ◽  
Diffraction Peaks

AbstractTwo crystals of the uranyl carbonate mineral grimselite, ideally K3Na[(UO2)(CO3)3](H2O), from Jáchymov in the Czech Republic were studied by single-crystal X-ray diffraction and electron-probe microanalysis. One crystal has considerably more Na than the ideal chemical composition due to substitution of Na into KO8 polyhedra; the composition of the other crystal is nearer to ideal, and similar to synthetic grimselite. The presence of Na atoms in KO8 polyhedra, which are located in channels in the crystal structure, reduces their volume, and as a result the unit-cell volume also decreases. Structure refinement shows that the formula for the sample with the anomalously high Na content is (K2.43Na0.57)Σ3.00Na[(UO2)(CO3)3](H2O). The unit-cell parameters, refined in space group P2c, are a = 9.2507(1), c = 8.1788(1) Å, V = 606.14(3) Å3 and Z = 2. The crystal structure was refined to R1 = 0.0082 and wR1 = 0.0185 with a GOF = 1.33, based on 626 observed diffraction peaks [Iobs>3σ(I)].

A Novel Hydroxyapatite Carrier for Enrichment of Hydrocarbon Degradation Bacteria

2007 ◽  
Vol 336-338 ◽  
pp. 1914-1917
Author(s):  
Lei Yang ◽  
Zhen Yi Zhang ◽  
Xiao Shan Ning ◽  
Guang He Li
Keyword(s):  
Activated Carbon ◽  
Sol Gel ◽  
Hydrocarbon Degradation ◽  
Potential Candidate ◽  
X Ray Diffraction ◽  
X Ray ◽  
Bacterial Enrichment ◽  
Bet Method ◽  
The One ◽  
Scanning Electron

In this paper, a novel and highly efficient hydroxyapatite (HA) carrier for cultivating hydrocarbon degradation bacteria (HDB) is introduced. The HA particles synthesized through a sol-gel method and different heat treatments were characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM) and BET method. The microbial amount and activities of HDB cultivated on HA carriers were quantitatively investigated in order to assess their enriching capabilities. The results showed that HA synthesized at 550°C and the one without calcination could enrich HDB 3 and 2 magnitude orders more than the activated carbon, respectively. Mechanisms of bacterial enrichment on HA and activated carbon were also studied, and it is believed that the high bioactivity and the surface morphology of HA were responsible for the efficient reproduction of HDB. It is concluded that HA is a potential candidate to replace the conventionally used activated carbon as a novel carrier applied in the filed of bioremediation for oil contaminated soil.

scholarly journals One-Pot Synthesis of Ru-Doped ZnO Oxides for Photodegradation of 4-Chlorophenol

2018 ◽  
Vol 2018 ◽  
pp. 1-12 ◽  
Author(s):  
Maria E. Manríquez ◽  
Luis Enrique Noreña ◽  
Jin An Wang ◽  
Lifang Chen ◽  
Jose Salmones ◽  
...  
Keyword(s):  
Band Gap ◽  
Mixed Oxides ◽  
Active Surface ◽  
Band Gap Energy ◽  
X Ray Diffraction ◽  
Electron Hole ◽  
One Pot ◽  
Notable Increase ◽  
Doped Zno ◽  
The One

The photocatalytic degradation of 4-chlorophenol in water using Ru-doped ZnO mixed oxides (0, 0.5, 1, and 3 wt% RuO2) synthesized by the one-pot homogeneous coprecipitation method is reported. ZnO with wurtzite structure was present in the mixed oxide as corroborated by Raman spectroscopy and X-ray diffraction analysis. All the samples showed nanorod morphological features. The presence of Ru6+/Ru4+ couples on ZnO modified the band gap of the mixed oxides and led to a shift of the band gap energy from 3.20 eV to 3.07 eV. Ru addition increased the surface area and significantly promoted the formation of active surface oxygen species such as hydroradicals evidenced by the fluorescence spectroscopy measurement. In the photodegradation of 4-chlorophenol solution under UV irradiation, a notable increase in photoactivity was obtained as the amount of RuO2 in the mixed oxides increased to 3 wt%. The charge transfer between Ru6+/Ru4+ couples and ZnO nanoparticles together with the formation of free radical oxidant species effectively inhibits electron-hole recombination rate, thus favoring the photodegradation of 4-chlorophenol.

Spontaneous formation of nanometer-scale self-organized structures in Ag-Cu alloys under irradiation

2000 ◽  
Vol 647 ◽  
Author(s):  
Raúl A. Enrique ◽  
Pascal Bellon
Keyword(s):  
Ion Irradiation ◽  
Ion Beam ◽  
Solute Concentration ◽  
Irradiation Temperature ◽  
Nanometer Scale ◽  
Beam Irradiation ◽  
X Ray Diffraction ◽  
Ion Beam Irradiation ◽  
Self Organized ◽  
The One

AbstractIon-beam irradiation can be used as a processing tool to synthesize metastable materials. A particular case is the preparation of solid solutions from immiscible alloys, which have been achieved for a whole range of systems. In this process, enhanced solute concentration is obtained through the local mixing induced by each irradiation event, which if occurring at a high enough frequency, can outweigh demixing by thermal diffusion. The resulting microstructure forms in far from equilibrium conditions, and theoretical results for these kind of driven alloys have shown that novel microstructures exhibiting self-organization can develop. To test these predictions, we prepare Ag-Cu multilayered thin films that we subject to 1 MeV Kr+-ion irradiation at temperatures ranging from room temperature to 225 °C, and characterize the specimens by x-ray diffraction, TEM and STEM. We observe two different phenomena occurring at different length scales: On the one hand, regardless of the irradiation temperature, grains grow under irradiation until reaching a size limited by film thickness (~200 nm). On the other hand, the distribution of species inside the grains is greatly affected by the irradiation temperature. At intermediate temperatures, a semi-coherent decomposition is observed at a nanometer scale. This nanometer-scale decomposition phenomenon appears as an evidence of patterning, and thus confirms on the possibility of using ion-beam irradiation as a route to synthesize nanostructured materials with novel magnetic and optical properties.

Polysulfonylamine, CXXV [1]. Neue Komplexe von Disulfonylaminen mit Kronenethern - im voraus entworfen oder zufällig entdeckt / Polysulfonylamines, CXXV [1]. New Complexes of Disulfonylam ines with Crown Ethers - Preconceived or Discovered by Serendipity

2000 ◽  
Vol 55 (3-4) ◽  
pp. 299-316 ◽  
Author(s):  
Dagmar Henschel ◽  
Karna Wijaya ◽  
Oliver Moers ◽  
Armand Blaschette ◽  
Peter G. Jones
Keyword(s):  
Hydrogen Bonds ◽  
X Ray Diffraction ◽  
Ladder Structure ◽  
Triclinic Space Group ◽  
One Dimensional ◽  
X Ray ◽  
Bonding System ◽  
Supramolecular Aggregate ◽  
Guest Species ◽  
The One

Abstract In a study aim ed at the „deconstruction“ of the supramolecular aggregate 3(18C6) · 2HN( SO2Me)2 (1,18C6 = 18-crown-6), which is known to display a ladder structure with two isotactic [18C6 - Me SO2N(H)SO2Me···)∞ polymers forming the uprights and symmetrically N - H···O bonded 18C6 rings providing the rungs, the following crystalline complexes were isolated and (except for 2b) characterized by low-temperature X-ray diffraction: 18C6-ClN (SO2Me)2 (2a, triclinic, space group P1̅, Z = 2), 18C6-PhN (SO2Me)2 (2b), 18C6 -MeN(SO2Me)2 (3, monoclinic, P21/c, Z = 8), Bz18C6-HN(SO2Me)2 (4, Bz18C6 = benzo-18-crown-6, monoclinic, P21/n, Z = 4), 18C6-2 MeN (SO2Me)2 (5, triclinic, P1̅, Z = 1), 18C6-Me2SO- HN( SO2Me) (SO2Ph) (13, triclinic, P1̅, Z = 2), and 18C6-H2OMe2SO·2HN(SO2Me)2 (14, triclinic, P1̅, Z = 2). Each of the one-dimensional polymers 2a (syndiotactic), 3 (disyndiotactic) and 4 (isotactic) mimics a single upright of 1; in contrast to 1 and 2a, where the intra-catemer connectivity solely relies on S - Me ··· crow n and crown ··· O = S hydrogen bonds, this bonding system is reinforced in 3 by N -Me ··· crown and in 4 by N - H ··· crown hydrogen bonds. Complex 5 is monomeric and matches a fragment formally extruded from the catemer 3; moreover, 3 and 5 represent a rare case of two structurally characterized 18C6 complexes containing the same uncharged guest species in distinct molecular ratios. The surprising structure of the quaternary adduct 14 exhibits an [18C6 ··· MeSO2N(H)SO2Me ··· ]∞ chain, which can be regarded both as an isolated, though unmodified upright from the ladder 1 and, being syndiotactic, as a stereochemical analogue of 2a; the potentially rung-forming *NH functions in the chain are blocked by hydrogenbonded side chains of the type * N - H ··· water ··· sulfoxide ··· H - N (SO2Me)2. The ternary complex 13 consists of chains [18C6 ··· Me2SO ··· H - N (SO2Ph)SO2Me···]∞ and is not closely related to the other structures

scholarly journals Формирование и трансформация моноклинной и орторомбической фаз в реакторных порошках сверхвысокомолекулярного полиэтилена

2018 ◽  
Vol 60 (9) ◽  
pp. 1847
Author(s):  
М.В. Байдакова ◽  
П.В. Дороватовский ◽  
Я.В. Зубавичус ◽  
Е.М. Иванькова ◽  
С.С. Иванчев ◽  
...  
Keyword(s):  
Mechanical Stress ◽  
Room Temperature ◽  
Monoclinic Phase ◽  
Orthorhombic Phase ◽  
Ultrahigh Molecular Weight Polyethylene ◽  
Polymer Synthesis ◽  
X Ray Diffraction ◽  
Reactor Powder ◽  
X Ray ◽  
The One

AbstractUsing powerful synchrotron X-ray radiation of the beamline “Belok” operated by the National Research Center “Kurchatov Institute,” we perform X-ray diffraction (XRD) study of an intact, virgin (not subjected to any external mechanical loads) particle isolated from reactor powder of ultrahigh molecular weight polyethylene. Along with the peaks originating from the orthorhombic phase, we detect the peaks characteristic of the monoclinic phase that is stable only under mechanical stress, suggesting that the mechanical stress that leads to the formation of the monoclinic phase and persists at room temperature develops during the polymer synthesis. The monoclinic phase gradually disappears when the particle is heated stepwise in increments of 5 K, and its peaks become undetectable when the temperature reaches 340 K. We contrast the results obtained for the phase composition of the virgin particle to those for a tablet prepared by compaction of the same reactor powder at room temperature. XRD analyses of the tablet were performed on D2 Phaser (Bruker) instrument. The monoclinic phase that originates during the polymer synthesis and the one that forms in the tablet during compaction have different parameters. We discuss the mechanisms by which these two different monoclinic phases originate during the processes involved.

scholarly journals The Technical Efficiency of Local Action Groups: a Czech Republic Case Study

2017 ◽  
Vol 65 (3) ◽  
pp. 1065-1074 ◽  
Author(s):  
Iveta Vrabková ◽  
Pavel Šaradín
Keyword(s):  
Czech Republic ◽  
Technical Efficiency ◽  
Comprehensive Evaluation ◽  
Local Action ◽  
Economic Returns ◽  
Evaluation Tool ◽  
The Czech Republic ◽  
The One ◽  
Action Groups

Local Action Groups (LAGs) represent a dynamic platform for inter-municipal cooperation in Europe. Their principal advantages include EU funding and the capacity to generate economic returns and stimulate the development of local communities. The methodology used for the evaluation of the performance of LAGs is defined by the EU on the one hand and by national authorities on the other. Furthermore, there are an entire array of evaluation tools and academic experiments available. The present paper does not aim at a comprehensive evaluation of LAGs, but instead only examines the technical efficiency of LAGs. Using the Czech Republic as an example, the paper introduces an evaluation tool to measure the technical efficiency of LAGs and describes how it can be applied. The adoption of this tool is seen as a means of improving one of the parameters of the performance of LAGs.

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