Journal articles on the topic 'Barium sulfide'

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1

Li, Pei Xin, Feng Qing Zhao, and Shao Jie Liu. "Preparation of Ultrafine Barium Sulfate Using Sodium Sulfate Content Wastewater." Advanced Materials Research 718-720 (July 2013): 96–101. http://dx.doi.org/10.4028/www.scientific.net/amr.718-720.96.

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The wastewater from folic acid production contains a large amount of sodium sulfate. In this paper, this sodium sulfate wastewater was used to react with the industry black salt (barium sulfide) to prepare barium sulfate. By adjusting the feeding mode, reaction temperature, reactant concentration and stirring speed, the optimal experimental condition was determined. The barium sulfates particle size under this condition was 320 nm, with good whiteness but low energy consumption. The product not only turns the waste to useful product successfully, but also meets Chinese policy of energy-saving, emission reduction and sustainable development.
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2

Kabdasli, Isik, Olcay Tünay, and Derin Orhon. "Sulfate removal from indigo dyeing textile wastewaters." Water Science and Technology 32, no. 12 (December 1, 1995): 21–27. http://dx.doi.org/10.2166/wst.1995.0451.

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Sulfate is an important parameter especially for discharges to sewer systems. The textile industry is a major source of sulfate. Some sulfate sources in the industry have material replacement alternatives. However in some sources, sulfate or species convertible to sulfate are the main materials. The indigo dyeing process involves sulfur species as main materials. In this study, indigo dyeing wastewaters which contain significant concentrations of oxidized and non-oxidized sulfur components are evaluated in terms of sulfate removal. The approach is a pretreatment at the source before being mixed with other wastewaters. The study is conducted in two steps. In the first step, conversion of species to either sulfide or sulfate is experimentally evaluated. While reduction to sulfide poses problems, oxidation of all species to sulfate is found to be applicable. In the second step sulfate precipitation using calcium, barium and lead is practiced. Calcium precipitation provides up to 30% sulfate removal and these results are supported with existing literature data. Barium sulfate and lead sulfate precipitation provided practically complete removal. Economical evaluation of alternative methods is also given.
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3

Yang, G. Y., Y. Bando, M. Saeki, and M. Onoda. "Structural characterizations of 6H-barium niobium sulfide." Acta Materialia 46, no. 17 (November 1998): 5985–92. http://dx.doi.org/10.1016/s1359-6454(98)00289-4.

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4

Tang, Yongjun, Darren R. Dunphy, and Richard A. Kemp. "Low-temperature preparation of crystalline barium sulfide." Applied Organometallic Chemistry 19, no. 6 (2005): 803–5. http://dx.doi.org/10.1002/aoc.890.

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5

Downs, James C. U., Deborah Milling, and Clay A. Nichols. "Suicidal Ingestion of Barium-Sulfide-Containing Shaving Powder." American Journal of Forensic Medicine and Pathology 16, no. 1 (March 1995): 56–61. http://dx.doi.org/10.1097/00000433-199503000-00013.

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6

Magnall, Joseph M., Sarah A. Gleeson, Robert A. Creaser, Suzanne Paradis, Johannes Glodny, and J. Richard Kyle. "The Mineralogical Evolution of the Clastic Dominant-Type Zn-Pb ± Ba Deposits at Macmillan Pass (Yukon, Canada)—Tracing Subseafloor Barite Replacement in the Layered Mineralization." Economic Geology 115, no. 5 (August 1, 2020): 961–79. http://dx.doi.org/10.5382/econgeo.4730.

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Abstract Clastic dominant-type massive sulfide deposits are well preserved in Upper Devonian carbonaceous mudstones in the Macmillan Pass district (Yukon, Canada). The Macmillan Pass deposits have been considered to be type examples of sedimentary exhalative Zn-Pb mineralization, whereby sulfides precipitated when hydrothermal fluids were vented into a euxinic (H2S-bearing) water column. We propose a new mineralization model, documenting the mineralogical evolution of layered mineralization. We show that textures previously interpreted to form via depositional processes actually formed by subseafloor replacement of diagenetic barite. Mineral assemblages associated with barite dissolution in the layered mineralization include (1) barium carbonate phases (witherite, barytocalcite, and norsethite), which are intergrown with Zn-Pb sulfides and represent localized Ba mass transfer, and (2) barium feldspar (celsian, hyalophane) that is abundant in the mudstones surrounding the layered mineralization. The barium feldspar formed following transport of Ba in low-sulfate fluids on the margins of the subseafloor replacement system. This resulted in whole-rock Ba enrichments (up to 5 wt %) in mudstones 15 m below and above the layered mineralization. High Ba in these surrounding mudstones is coupled with decreasing K/Al ratios, indicative of secondary illite and kaolinite. The source(s) of fluids related to the diagenetic (barite, barytocalcite) and hydrothermal (ankerite) assemblages can be constrained using Sr isotopes. Whereas highly radiogenic 87Sr/86Sr values (>0.714) in ankerite correspond with host-rock alteration within the vent complex, the overlying barite and barytocalcite preserve lower 87Sr/86Sr values (<0.714), providing evidence of mixing between a radiogenic fluid (likely a formation water) and Late Devonian seawater. The complex mineralogy and paragenesis contained within the layered mineralization are linked to a protracted history of diagenetic and hydrothermal fluid events, all of which took place in and peripheral to a subseafloor replacement hydrothermal system.
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7

Gaikwad, Amit A., Niyantha Challapalli, and Ashok N. Bhaskarwar. "CARBONATION OF BARIUM SULFIDE IN A FOAM-BED REACTOR." Chemical Engineering Communications 197, no. 6 (February 22, 2010): 804–29. http://dx.doi.org/10.1080/00986440903359103.

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8

Nozaki, Hiroshi, Masanobu Saeki, and Mitsuko Onoda. "Superconducting and Normal State Properties of Barium Tantalum Sulfide." Journal of Solid State Chemistry 116, no. 2 (May 1995): 392–99. http://dx.doi.org/10.1006/jssc.1995.1231.

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9

Lin, Yu-Feng, Yen-Hwei Chang, Yee-Shin Chang, Bin-Siang Tsai, and Yu-Chun Li. "Luminescent Properties of Trivalent Praseodymium-Doped Barium Zinc Sulfide." Journal of The Electrochemical Society 153, no. 6 (2006): G543. http://dx.doi.org/10.1149/1.2189968.

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10

Pathak, C. S., D. D. Mishra, V. Agarwala, and M. K. Mandal. "Blue light emission from barium doped zinc sulfide nanoparticles." Ceramics International 38, no. 7 (September 2012): 5497–500. http://dx.doi.org/10.1016/j.ceramint.2012.03.063.

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11

Matsuura, Kiyotaka, Takahiro Wada, Takashi Nakamizo, H. Yamauchi, and Shoji Tanaka. "Physical properties of a new barium niobium sulfide, BaNb2S5." Journal of Solid State Chemistry 94, no. 2 (October 1991): 294–97. http://dx.doi.org/10.1016/0022-4596(91)90194-m.

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12

Maskaeva, Larisa N., Ekaterina E. Lekomtseva, Anastasia D. Kutyavina, and Vyacheslav F. Markov. "Effect of barium salt on deposition kinetics, morphology and composition of chemically precipitated PbS films." Butlerov Communications 58, no. 5 (May 31, 2019): 90–97. http://dx.doi.org/10.37952/roi-jbc-01/19-58-5-90.

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Thin films of lead sulfide obtained by various physicochemical methods are widely used as IR detectors, ion-selective sensors, sensors of temperature and humidity, in solar radiation converters due to a high absorption coefficient in the infrared spectrum of 1-3 μm. Researchers note technological simplicity, the absence of high temperatures and vacuum, as well as the possibility of light doping of lead sulfide films during their production by chemical bath deposition from aqueous media. In the present work, we studied the kinetics of hydrochemical deposition of the solid PbS phase from the ammonium citrate reaction mixture. The introduction of barium chloride BaCl2 into the reactor in the concentration range from 0.5∙10-5 to 5∙10-3 mol/l has led to an increase in the induction deposition period from 5 to 30 minutes. In this work, polycrystalline films of individual lead sulfide were synthesized, as well as PbS layers doped with iodine and additionally barium with salt content in the last mixtures from 0.5∙10-5 to 5∙10-3 mol/l. The film thickness varied from 350 to 210 nm. An elemental EDX analysis of the obtained PbS films was performed. For the main components contained in the layers (Pb and S), insignificant non-stoichiometry in composition was established. The morphology of films of PbS during their doping with iodine and barium undergoes significant changes. Thus, if an individual PbS is formed from particles whose average size is 250 nm, then introduction of ammonium iodide into the solution leads to the appearance of grains with an average size of 150-200 nm, and adding the barium salt results a slight increase in the grain size up to 150-300 nm. The share of nanoparticles in these layers is 1-4%. The histograms of the distribution of particles in the films, both for individual and doped PbS, are monomodal.
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13

Mukdeeprom-Burckel, Pannee, and Jimmie G. Edwards. "Chemistry and thermodynamics of solid and vapor phases in the barium-sulfide, gallium-sulfide system." Materials Research Bulletin 25, no. 2 (February 1990): 163–72. http://dx.doi.org/10.1016/0025-5408(90)90042-z.

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14

Maeda, Kouji, Nao Kawaida, Ryutaro Tsudome, Kentaro Sakai, and Tetsuo Ikari. "X-ray and photoluminescence properties of Sm3+ doped barium sulfide." physica status solidi (c) 9, no. 12 (November 9, 2012): 2271–74. http://dx.doi.org/10.1002/pssc.201200321.

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15

Plichta, Edward J., and Wishvender K. Behl. "High rate molten salt cells employing barium nickel sulfide cathodes." Journal of Power Sources 37, no. 3 (February 1992): 325–33. http://dx.doi.org/10.1016/0378-7753(92)85016-4.

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16

Rino, José Pedro. "An interaction potential for barium sulfide: A molecular dynamics study." Computational Materials Science 92 (September 2014): 334–42. http://dx.doi.org/10.1016/j.commatsci.2014.05.053.

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17

Saeki, Masanobu, and Mitsuko Onoda. "Preparation and Crystal Structure of a New Barium Niobium Sulfide, Ba9Nb4S21." Bulletin of the Chemical Society of Japan 64, no. 10 (October 1991): 2923–25. http://dx.doi.org/10.1246/bcsj.64.2923.

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18

Addadi, Zoubida, Bendouma Doumi, Allel Mokaddem, Mohammed Elkeurti, Adlane Sayede, Abdelkader Tadjer, and Fethallah Dahmane. "Electronic and Ferromagnetic Properties of 3d(V)-Doped (BaS) Barium Sulfide." Journal of Superconductivity and Novel Magnetism 30, no. 4 (November 7, 2016): 917–23. http://dx.doi.org/10.1007/s10948-016-3894-3.

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19

Bouznit, Y., and Y. Beggah. "Comment on “Blue light emission from barium doped zinc sulfide nanoparticles”." Ceramics International 39, no. 8 (December 2013): 9845–46. http://dx.doi.org/10.1016/j.ceramint.2013.05.037.

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20

Stinn, Caspar, Katsuhiro Nose, Toru Okabe, and Antoine Allanore. "Experimentally Determined Phase Diagram for the Barium Sulfide-Copper(I) Sulfide System Above 873 K (600 °C)." Metallurgical and Materials Transactions B 48, no. 6 (October 4, 2017): 2922–29. http://dx.doi.org/10.1007/s11663-017-1107-5.

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21

Kosheleva, E. V., M. A. Pentin, L. A. Kalinina, T. V. Mikhailichenko, T. A. Lapteva, and Yu N. Ushakova. "Heterogeneous doping of sulfide-conducting phases based on calcium and barium thiolanthanates." Russian Journal of Electrochemistry 53, no. 7 (July 2017): 790–98. http://dx.doi.org/10.1134/s1023193517070059.

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22

Zilevu, Daniel, and Sidney E. Creutz. "Shape-Controlled Synthesis of Colloidal Nanorods and Nanoparticles of Barium Titanium Sulfide." Chemistry of Materials 33, no. 13 (June 22, 2021): 5137–46. http://dx.doi.org/10.1021/acs.chemmater.1c01193.

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23

Zhang, Wei, Yong Zhou, Jiahua Zhu, and Yanlin Pan. "New Clean Process for Barium Sulfide Preparation by Barite Reduction with Elemental Sulfur." Industrial & Engineering Chemistry Research 53, no. 14 (March 28, 2014): 5646–51. http://dx.doi.org/10.1021/ie4042356.

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24

SAEKI, M., and M. ONODA. "ChemInform Abstract: Preparation and Crystal Structure of a New Barium Niobium Sulfide, Ba9Nb4S21." ChemInform 23, no. 1 (August 22, 2010): no. http://dx.doi.org/10.1002/chin.199201033.

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25

Zagorac, Dejan, Jelena Zagorac, Klaus Doll, Maria Cebela, and Branko Matovic. "Extreme pressure conditions of bas based materials: Detailed study of structural changes, band gap engineering, elastic constants and mechanical properties." Processing and Application of Ceramics 13, no. 4 (2019): 401–10. http://dx.doi.org/10.2298/pac1904401z.

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A Density Functional Theory (DFT) study has been performed in order to investigate behaviour of barium sulfide (BaS) at high pressures, and relationship between computed properties, in great detail. Novel predicted and previously synthesized BaS modifications have been calculated using Local Density Approximations (LDA) and Generalized Gradient Approximation (GGA) functionals. In particular, a detailed investigation of structural changes and its corresponding volume effect up to 100GPa, with gradual pressure increase, has been performed from the first principles. Band gap engineering of the experimentally observed BaS phases at high pressures has been simulated and structure-property relationship is investigated. For each of the predicted and experimentally observed BaS structures, elastic constants and mechanical properties under compression have been investigated (e.g. ductility/brittleness, hardness, anisotropy). This study offers a new perspective of barium sulphide as a high pressure material with application in ceramics, optical and electrical technologies.
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26

Qin, Chengbing, and Timothy C. Steimle. "Optical Stark spectroscopy of the (3,0) A1Σ+–X1Σ+ band system of barium sulfide, BaS." Journal of Molecular Spectroscopy 281 (November 2012): 1–3. http://dx.doi.org/10.1016/j.jms.2012.09.003.

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27

Zhang, Zemin, Xiaodong Li, Caitian Gao, Feng Teng, Youqing Wang, Lulu Chen, Weihua Han, Zhenxing Zhang, and Erqing Xie. "Synthesis of cadmium sulfide quantum dot-decorated barium stannate nanowires for photoelectrochemical water splitting." Journal of Materials Chemistry A 3, no. 24 (2015): 12769–76. http://dx.doi.org/10.1039/c5ta01948f.

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28

Maskaeva, L. N., E. V. Mostovshchikova, V. I. Voronin, E. E. Lekomtseva, P. S. Bogatova, and V. F. Markov. "Structure, Optical, and Photoelectric Properties of Lead-Sulfide Films Doped with Strontium and Barium." Semiconductors 54, no. 10 (October 2020): 1230–40. http://dx.doi.org/10.1134/s1063782620100231.

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29

Sifi, C., F. Chouit, H. Bendjeddou, H. Meradji, and S. Ghemid. "Results of optical and thermal study of lead sulfide (PbS), Barium sulfide (BaS) and their ternary (Pb1-xBaxS) (0≤x≤1)alloys." Computational Condensed Matter 21 (December 2019): e00398. http://dx.doi.org/10.1016/j.cocom.2019.e00398.

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30

Absike, H., H. Labrim, B. Hartiti, and H. Ez-Zahraouy. "Effects of Si Doping on the Structural, Electronic and Optical Properties of Barium Chalcogenide BaS: A First-Principles Study." SPIN 10, no. 02 (June 2020): 2050014. http://dx.doi.org/10.1142/s2010324720500149.

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In this work, the structural, electronic and optical properties of Si-doped barium chalcogenide [barium sulfide (BaS)] with different Si concentrations ([Formula: see text]) are investigated by the first-principles calculations based on the density functional theory (DFT). The band structures, charge densities and complex dielectric functions of the pure as well as Si-doped BaS were presented and analyzed in detail using TB-mBJ approach by WIEN2k package. It is found that silicon concentration can control the bandgap by reducing it to values around 1.4[Formula: see text]eV and 1.6[Formula: see text]eV for 12.5% and 6.25% of Si-doped BaS, respectively. The electron charge density indicates the ionic bonding between silicon and sulfur atoms due to the high electronegativity between them. In fact, the results show that the absorption peaks of Si-doped BaS are enhanced compared with pure BaS. These results suggest that the Ba[Formula: see text]SixS original structure displays excellent physical properties thereby revealing that it is a promising material in advanced optoelectronic and solar cell applications.
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Nakamura, Takato, Masato Kamiya, Hiromichi Watanabe, and Yoichiro Nakanishi. "Preparation and Characterization of Zinc Sulfide Phosphors Coated with Barium Titanate Using Sol‐Gel Method." Journal of The Electrochemical Society 142, no. 3 (March 1, 1995): 949–52. http://dx.doi.org/10.1149/1.2048564.

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32

Konieczna, Monika, Ewa Markiewicz, and Jan Jurga. "Dielectric properties of polyethylene terephthalate/polyphenylene sulfide/barium titanate nanocomposite for application in electronic industry." Polymer Engineering & Science 50, no. 8 (April 6, 2010): 1613–19. http://dx.doi.org/10.1002/pen.21687.

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33

Dempsey, E. D., R. E. Holdsworth, D. Selby, A. Bird, B. Young, and C. Le Cornu. "A revised age, structural model and origin for the North Pennine Orefield in the Alston Block, northern England: intrusion (Whin Sill)-related base metal (Cu–Pb–Zn–F) mineralization." Journal of the Geological Society 178, no. 4 (February 4, 2021): jgs2020–226. http://dx.doi.org/10.1144/jgs2020-226.

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Mineralization and associated fluid migration events in the c. 1500 km2 North Pennine Orefield (NPO) are known to be associated with tectonic activity, but the age of these tectonic events and origins of the base metal sulfide mineralization remain unresolved. New fieldwork in the Alston Block shows that mineralization post-dates a weakly developed phase of north–south shortening consistent with far-field Variscan basin inversion during the late Carboniferous. New observations of field relationships, coupled with microstructural observations and stress inversion analyses, together with Re–Os sulfide geochronology show that the vein-hosted mineralization (apart from barium minerals) was synchronous with a phase of north–south extension and east–west shortening coeval with emplacement of the Whin Sill (c. 297–294 Ma). Thus the development of the NPO was related to an early Permian regional phase of transtensional deformation, mantle-sourced hydrothermal mineralization and magmatism in northern Britain. Previously proposed Mississippi Valley Type models, or alternatives relating mineralization to the influx of Mesozoic brines, can no longer be applied to the development of the NPO in the Alston Block. Our findings also mean that existing models for equivalent base metal sulfide fields worldwide (e.g. Zn–Pb districts of Silesia, Poland and Tennessee, USA) may need to be reassessed.
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Zhang, Wei, Fengzhen Zhang, Liping Ma, Jie Yang, Jing Yang, and Huaping Xiang. "Reaction mechanism study of new scheme using elemental sulfur for conversion of barite to barium sulfide." Powder Technology 360 (January 2020): 1348–54. http://dx.doi.org/10.1016/j.powtec.2019.10.088.

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35

Spangenberg, Jorge E., Nicolas J. Saintilan, and Sabina Strmić Palinkaš. "Safe, accurate, and precise sulfur isotope analyses of arsenides, sulfarsenides, and arsenic and mercury sulfides by conversion to barium sulfate before EA/IRMS." Analytical and Bioanalytical Chemistry 414, no. 6 (January 23, 2022): 2163–79. http://dx.doi.org/10.1007/s00216-021-03854-y.

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AbstractThe stable isotope ratios of sulfur (δ34S relative to Vienna Cañon Diablo Troilite) in sulfates and sulfides determined by elemental analysis and isotope ratio mass spectrometry (EA/IRMS) have been proven to be a remarkable tool for studies of the (bio)geochemical sulfur cycles in modern and ancient environments. However, the use of EA/IRMS to measure δ34S in arsenides and sulfarsenides may not be straightforward. This difficulty can lead to potential health and environmental hazards in the workplace and analytical problems such as instrument contamination, memory effects, and a non-matrix-matched standardization of δ34S measurements with suitable reference materials. To overcome these practical and analytical challenges, we developed a procedure for sulfur isotope analysis of arsenides, which can also be safely used for EA/IRMS analysis of arsenic sulfides (i.e., realgar, orpiment, arsenopyrite, and arsenian pyrite), and mercury sulfides (cinnabar). The sulfur dioxide produced from off-line EA combustion was trapped in an aqueous barium chloride solution in a leak-free system and precipitated as barium sulfate after quantitative oxidation of hydrogen sulfite by hydrogen peroxide. The derived barium sulfate was analyzed by conventional EA/IRMS, which bracketed the δ34S values of the samples with three international sulfate reference materials. The protocol (BaSO4-EA/IRMS) was validated by analyses of reference materials and laboratory standards of sulfate and sulfides and achieved accuracy and precision comparable with those of direct EA/IRMS. The δ34S values determined by BaSO4-EA/IRMS in sulfides (arsenopyrite, arsenic, and mercury sulfides) samples from different origins were comparable to those obtained by EA/IRMS, and no sulfur isotope fractionations were introduced during sample preparation. We report the first sulfur isotope data of arsenides obtained by BaSO4-EA/IRMS. Graphical abstract
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Liu, Wenguo, Xiangdong Xing, and Haibin Zuo. "Effect of TiO2 on Viscosity and Sulfide Capacity of Blast Furnace Slag Containing Barium." ISIJ International 60, no. 9 (September 15, 2020): 1886–91. http://dx.doi.org/10.2355/isijinternational.isijint-2019-627.

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Zagorac, Dejan, Klaus Doll, Jelena Zagorac, Dragana Jordanov, and Branko Matović. "Barium Sulfide under Pressure: Discovery of Metastable Polymorphs and Investigation of Electronic Properties on ab Initio Level." Inorganic Chemistry 56, no. 17 (August 24, 2017): 10644–54. http://dx.doi.org/10.1021/acs.inorgchem.7b01617.

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Li, He, and Shiou-Jyh Hwu. "Electrochemical Synthesis of Ba2Ag8S7, a Quasi-One-Dimensional Barium Silver(I) Sulfide Containing Mixed S2−/S22− Ligands." Angewandte Chemie International Edition 38, no. 20 (October 18, 1999): 3067–70. http://dx.doi.org/10.1002/(sici)1521-3773(19991018)38:20<3067::aid-anie3067>3.0.co;2-b.

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39

NAKAMURA, T., M. KAMIYA, H. WATANABE, and Y. NAKANISHI. "ChemInform Abstract: Preparation and Characterization of Zinc Sulfide Phosphors Coated with Barium Titanate Using Sol-Gel Method." ChemInform 26, no. 29 (August 17, 2010): no. http://dx.doi.org/10.1002/chin.199529328.

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40

Klochkova, N. V., A. V. Ananyev, N. Yu Pozdnyakova, and A. A. Savelyev. "USING AEROBIC SYNTROPHIC ASSOCIATIONS OF MICROORGANISMS FOR THE DECONTAMINATION OF LIQUID RADIOACTIVE WASTE." Fine Chemical Technologies 13, no. 6 (December 28, 2018): 52–59. http://dx.doi.org/10.32362/2410-6593-2018-13-6-52-59.

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The primary objective of the study was to test the possibility of cesium-137 transmutation into a stable barium isotope in contact with an aerobic syntrophic association (SA - a conglomerate of several thousands of different species of bacteria, protozoa and fungi living in symbiosis with each other) together with a set of macro- and microelements. The study was performed sequentially on two different SA. In the course of the work, the transmutation of cesium-137 into stable barium with the use of SA was not experimentally revealed, but the phenomenon of cesium-137 biosorption by both SA was detected to different degrees. In the course of the experiment the possibility of cesium-137 sorption by SA from the solution in the pH range of 7.7 - 8.6 was shown. In the process of the work, the time dependence of cesium-137 distribution in the liquid phase and the phase of SA was determined. The time dependence of the sorption capacity of the syntrophic association was revealed. With further continuation of the study, it is possible to obtain a mixture of SA capable of selectively extracting and concentrating prescribed radionuclides from the liquid phase.The result of this work may be the development of a technology for processing and conditioning low-level liquid radioactive waste (RW) by transferring the bulk of radioisotopes in the phase of SA (the so-called "nanosorbent of biological origin"), with multiple volume reduction.The cost of such a technology compared to existing technologies using synthetic sorbents should be several times less due to the cheapness of the SA and the reagents required for it. Besides, the new technology is more environmentally friendly. The process of biotechnologyoxidation of sulfide ores and concentrates based on the activity of chemolitotrophic bacteria that translate insoluble metal sulfides into soluble metal sulfates can serve as analogue for hardware design of RW purification technology using nanosorbent of biological origin.
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41

Subedi, Kamala Khanal, Ebin Bastola, Indra Subedi, Sandip S. Bista, Suman Rijal, Manoj K. Jamarkattel, Rasha A. Awni, et al. "Semi-transparent p-type barium copper sulfide as a back contact interface layer for cadmium telluride solar cells." Solar Energy Materials and Solar Cells 218 (December 2020): 110764. http://dx.doi.org/10.1016/j.solmat.2020.110764.

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42

Snyder, G. Jeffrey, Michael E. Badding, and F. J. DiSalvo. "Synthesis, structure, and properties of barium cobalt sulfide (Ba6Co25S27) a perovskite-like superstructure of Co8S6 and Ba6S clusters." Inorganic Chemistry 31, no. 11 (May 1992): 2107–10. http://dx.doi.org/10.1021/ic00037a024.

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Kim, Doory. "Recent Developments in Lanthanide-Doped Alkaline Earth Aluminate Phosphors with Enhanced and Long-Persistent Luminescence." Nanomaterials 11, no. 3 (March 13, 2021): 723. http://dx.doi.org/10.3390/nano11030723.

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Lanthanide-activated alkaline earth aluminate phosphors are excellent luminescent materials that are designed to overcome the limitations of conventional sulfide-based phosphors. The increasing research attention on these phosphors over the past decade has led to a drastic improvement in their phosphorescence efficiencies and resulted in a wide variety of phosphorescence colors, which can facilitate applications in various areas. This review article discusses the development of lanthanide-activated alkaline earth aluminate phosphors with a focus on the various synthesis methods, persistent luminescence mechanisms, activator and coactivator effects, and the effects of compositions. Particular attention has been devoted to alkaline earth aluminate phosphors that are extensively used, such as strontium-, calcium-, and barium-based aluminates. The role of lanthanide ions as activators and coactivators in phosphorescence emissions was also emphasized. Finally, we address recent techniques involving nanomaterial engineering that have also produced lanthanide-activated alkaline earth aluminate phosphors with long-persistent luminescence.
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44

Li, He, and Shiou-Jyh Hwu. "ChemInform Abstract: Electrochemical Synthesis of Ba2Ag8S7, a Quasi-One-Dimensional Barium Silver(I) Sulfide Containing Mixed S2-/S22- Ligands." ChemInform 31, no. 1 (June 12, 2010): no. http://dx.doi.org/10.1002/chin.200001026.

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45

Kravchishina, M. D., A. Yu Lein, A. G. Boev, V. Y. Prokofiev, D. P. Starodymova, O. M. Dara, A. N. Novigatsky, and A. P. Lisitzin. "Hydrothermal mineral associations on 71° n of Mid-Atlantic ridge (first results)." Океанология 59, no. 6 (December 22, 2019): 1039–57. http://dx.doi.org/10.31857/s0030-15745961039-1057.

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We discuss the preliminary results of the plume and bottom sediments studies of the Trollveggen hydrothermal vent field based on data from the 68th cruise of the RV Akademik Mstislav Keldysh. The hydrothermal vent field is located to the east of the axial zone of the slow-spreading Mohn Ridge close to the Jan Mayen hotspot at a depth of about 550 m (7118 'N, Norwegian-Greenland Basin). The plume of the hydrothermal vent field was characterized by a weak distribution in the water column, anomalies of temperature, density and salinity, a moderate concentration of methane and a low concentration of suspended particulate matter near the bottom. The enrichment of bottom sediments with barium, strontium and some sulfide forming elements (zinc, lead, copper, molybdenum) was shown. Two mineral associations of hydrothermally modified bottom sediments were revealed: pyrite and barite-marcasite. The temperature of hydrothermal fluids was established by the method of thermal and cryometric studies of gas-liquid fluid inclusions in barite (128260C) and using the FeSZnS equilibrium diagram of sulfide minerals (130290C). Our data were close to the data of direct measurements of fluid temperature [28]. We made a comparison of the hydrothermal mineralization of the Trollveggen vent field and the previously studied fields of the Mid-Atlantic Ridge located near the Azores hotspot. As a result we confirmed the influence of ocean depth and PT-conditions on the formation of hydrothermal deposits.
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Smirnov, A. N., and V. G. Solomonik. "Spectroscopic Properties of the Barium Sulfide Molecule in Its Low-Lying Electronic States X1Σ+, a3Π, A'1Π, b3Σ+, and A1Σ+." Russian Journal of Physical Chemistry A 94, no. 5 (May 2020): 956–62. http://dx.doi.org/10.1134/s0036024420050210.

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47

Al-Ghamdi, Rasha A., and Husin Sitepu. "Characterization of Sludge Deposits from Refineries and Gas Plants: Prerequisite Results Requirements to Facilitate Chemical Cleaning of the Particular Equipment." International Journal of Corrosion 2018 (September 2, 2018): 1–8. http://dx.doi.org/10.1155/2018/4121506.

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In this paper, the method developed by the authors to separate the inorganic materials from the hydrocarbon of the sludge deposits, which is fast and can accurately identify very small quantities of inorganic materials, has been extended to characterize the 12 types of sludge samples collected from (a) a regeneration overhead acid gas condenser, (b) water draw-off pump’s suction strainer in a gas plant, and (c) condenser, inside vessels of inlet head, and head coiler tube equipment at gas plants. The results revealed that the major phases are (a) iron sulfide corrosion products with the hydrocarbon type of mixture of diesel and lube oil for a condenser and (b) carbonate scale in the form of calcium carbonate with the hydrocarbon type of lubricant oil for sludge deposits from a suction strainer for pumps, and drilling mud in the form of barium sulfate with no organic hydrocarbon or polymer for sludge samples from a water recycling pump. Moreover, the major phases for inorganic materials built up in a condenser, inside the vessel’s inlet head, and the head coiler tube revealed that iron oxide corrosion products are found in the steam drum, and iron sulfate corrosion products are built up in the condenser. The presence of dissolved oxygen in the boiler feed water is indicated by a high wt% of iron oxide corrosion product in the form of magnetite (Fe3O4), which appeared in the inorganic materials built up in the condenser steam drum. Knowing accurately which phases and their wt% were involved in the inorganic materials can guide the field engineers to facilitate efficient cleaning of the equipment by drawing up the right procedures and taking preventive action to stop the generation of those particular sludge deposits.
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Xie, Rui, Daidai Wu, Jie Liu, Tiantian Sun, Lihua Liu, and Nengyou Wu. "Geochemical Evidence of Metal-Driven Anaerobic Oxidation of Methane in the Shenhu Area, the South China Sea." International Journal of Environmental Research and Public Health 16, no. 19 (September 23, 2019): 3559. http://dx.doi.org/10.3390/ijerph16193559.

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Anaerobic oxidation of methane (AOM) is a common biochemical process in the ocean and it plays an important role in global climate change, elemental circulation, and atmospheric evolution over geological time. In this paper, we analyzed of δ34S, Fe, Mn, Ca/Ti, and Sr/Ti ratios, and the date of carbon and sulfur from the site SH3 of Shenhu area. Result showed that (1) 0–6 mbsf (meter blow the sea floor) was mainly affected by OSR (anaerobic oxidation of organic matters) and 7–15 mbsf was a paleo-SMTZ (sulfate–methane transition zone) position. The modern SMTZ was mainly distributed at 19–25 mbsf. The barium sulfate precipitation above the modern SMTZ indicating that the current methane leakage was stable and lasted longer during geological history. (2) By studying the change of magnetic and the different carbonate minerals, results showed that there were two AOM stages. During the early stage, Fe2+ were mainly produced by sulfide abiotic reductive dissolution. During the later stage, Fe2+ were mainly produced by the metal-AOM. (3) Study of the mineral characteristics of the paleo-SMTZ and the modern SMTZ showed that the modern SMTZ carbonate minerals were mainly low-Mg calcite and aragonite, while the paleo-SMTZ carbon minerals were mainly high Mg minerals. The reason for this difference is that the modern SMTZ layer was only experienced the first stage of anaerobic oxidation of methane. In the paleo-SMTZ layer, it has experienced two stage of anaerobic oxidation of methane. During the last stage of metal-AOM, the low Mg carbonate minerals were converted into high Mg carbonate minerals. This research confirms the presence of metal-driven methane anaerobic oxidation at the bottom of sulfate-driven methane anaerobic oxidation and during the metal-driven methane anaerobic oxidation, methane and metal oxides or hydroxides would couple to convert the in situ metal oxides or hydroxides into metal ions, meanwhile the phosphorus adsorbed on the surface of the metal oxides is released into adjacent pore water, and convert to new P-bearing minerals under suitable conditions.
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Jones, Franca, Mark I. Ogden, and Tomoko Radomirovic. "The impact of sulfite ions on barium sulfate crystallization." Journal of Crystal Growth 507 (February 2019): 213–19. http://dx.doi.org/10.1016/j.jcrysgro.2018.11.022.

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&NA;. "Barium sulfate." Reactions Weekly &NA;, no. 1215 (August 2008): 10. http://dx.doi.org/10.2165/00128415-200812150-00030.

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