Relevant bibliographies by topics / Alkaline earth metals

Academic literature on the topic 'Alkaline earth metals'

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Published: 4 June 2021
Last updated: 29 July 2024

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Journal articles on the topic "Alkaline earth metals"

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Hill, Michael S. "Alkaline and alkaline earth metals." Annual Reports Section "A" (Inorganic Chemistry) 108 (2012): 48. http://dx.doi.org/10.1039/c2ic90011d.

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Hill, Michael S. "Alkaline and alkaline earth metals." Annual Reports Section "A" (Inorganic Chemistry) 106 (2010): 39. http://dx.doi.org/10.1039/b918367c.

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Hill, Michael S. "Alkaline and alkaline earth metals." Annual Reports Section "A" (Inorganic Chemistry) 109 (2013): 18. http://dx.doi.org/10.1039/c3ic90010j.

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Hill, Michael S. "Alkaline and alkaline earth metals." Annual Reports Section "A" (Inorganic Chemistry) 107 (2011): 43. http://dx.doi.org/10.1039/c1ic90016a.

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Hill, Michael S. "ChemInform Abstract: Alkaline and Alkaline Earth Metals." ChemInform 43, no. 43 (September 27, 2012): no. http://dx.doi.org/10.1002/chin.201243224.

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Hill, Michael S. "ChemInform Abstract: Alkaline and Alkaline Earth Metals." ChemInform 44, no. 52 (December 5, 2013): no. http://dx.doi.org/10.1002/chin.201352225.

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Hopkins, Alexander D. "Alkali and alkaline-earth metals." Annual Reports Section "A" (Inorganic Chemistry) 102 (2006): 46. http://dx.doi.org/10.1039/b508351f.

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Hill, Michael S. "Alkali and alkaline-earth metals." Annual Reports Section "A" (Inorganic Chemistry) 105 (2009): 55. http://dx.doi.org/10.1039/b818133k.

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Peterson, David T. "Purification of Alkaline Earth Metals." JOM 39, no. 5 (May 1987): 20–23. http://dx.doi.org/10.1007/bf03258986.

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Hill, Michael S. "Alkali and alkaline-earth metals." Annual Reports Section "A" (Inorganic Chemistry) 103 (2007): 39. http://dx.doi.org/10.1039/b612595f.

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Dissertations / Theses on the topic "Alkaline earth metals"

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Ovchinnikov, Alexander. "Nitridomanganates of alkaline-earth metals." Doctoral thesis, Saechsische Landesbibliothek- Staats- und Universitaetsbibliothek Dresden, 2016. http://nbn-resolving.de/urn:nbn:de:bsz:14-qucosa-215891.

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The main goal of the present work was the synthesis of alkaline-earth nitridomanganates (AExMnyNz) with extended anionic structures and the characterization of their electronic and magnetic properties. Up to now, only compounds with isolated nitridomanganate anions have been reported in the discussed ternary systems. A systematic exploratory synthesis, employing high-temperature treatment of AE nitrides and Mn under controlled N2 pressure, yielded more than ten new nitridomanganates. Their crystal structures contain anionic building blocks of different dimensionalities, ranging from isolated species to three-dimensional frameworks. In general, the formation of Mn-rich compositions was found to be driven by the emergence of Mn-Mn interactions, which creates a link between nitridometalates and transition-metal-rich binary nitrides. The obtained nitridomanganates display a plethora of interesting phenomena, such as large spin-orbit coupling, magnetic frustration, quenching of magnetism due to Mn-Mn interactions, and metal-insulator transition.
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Miller, Stewart Anthony Stephen. "Alkaline earth and cerium compounds." Thesis, University of Liverpool, 1995. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.283730.

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Day, S. "Neutron and optical spectroscopy of alkaline earth metals." Thesis, University of Oxford, 1988. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.234944.

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Elhiyani, Mohamed. "Study of helium clusters doped with alkaline-earth metals." Phd thesis, Université Paris-Est, 2009. http://tel.archives-ouvertes.fr/tel-00584392.

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Ces dernières années, les agrégats d'hélium superfluides ont fait l'objet de nombreuses études aussi bien expérimentales que théoriques. Le fruit de ces études a permis le développement de méthodes spectroscopiques innovantes (HENDI) utilisant les nanogouttes d'hélium comme l'ultime matrice, exploitant ainsi la très faible température de ce milieu particulier et sa faible interaction avec les dopants pour une meilleure résolution spectrale. Cependant, un nombre important de questions subsiste quant aux agrégats d'hélium dopés, particulièrement, ceux dopés par les alcalino-terreux. En effet, la position d'une impureté au sein de la gouttelette d'hélium est loin d'être un problème trivial pour certaines espèces telles les alcalino-terreux. Ceci est particulièrement vrai dans le cas où l'impureté est l'atome de magnésium. Des preuves expérimentales d'un état solvaté du magnésium sont annoncées dans la littérature tandis que de récentes expériences laissent penser à une position plutôt surfacique du magnésium dans les agrégats d'hélium. Du point de vue théorique, la même ambiguïté persiste quant à la position de Mg dans la nanogoutte d'hélium. Dans le but de contribuer à une meilleure compréhension des clusters d'hélium dopés par les métaux alcalino-terreux (Mg et Ca), nous avons, au cours de ce travail, dû déterminer avec précision les énergies d'interactions des états fondamentaux des systèmes van der Waals CaHe et MgHe. Pour ce faire, des méthodes ab initio telles les approches des clusters couplés (CC) mais aussi perturbationnelles (MP2 et MP4) ont été appliquées à ces deux systèmes avec succès. Les meilleurs potentiels d'interaction ont été utilisés par la suite comme potentiels d'interactions de paire dans l'approche Monte Carlo à diffusion (DMC) en combinaison de deux types de potentiel d'interaction pour l'hélium. Aussi bien pour CaHen que pour MgHen, des simulations DMC ont été produites depuis n = 1 jusqu'à n = 220, le résultat principal en est une position surfacique de l'impureté quelque soit l'alcalino-terreux considéré. Dans le cas particulièrement délicat des clusters d'hélium dopés par le magnésium, des calculs de DMC avec des contraintes géométriques montrent que le potentiel radial effectif de Mg dans He20 et He50 est plutôt plat. Enfin, sont présentés également les résultats concernant la recombinaison dynamique de deux atomes de magnésium à l'intérieur d'un agrégat d'environ 2000 atomes d'hélium utilisant une méthode basée sur un potentiel effectif pour l'interaction He-He
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Guino-o, Marites A. "Placing heavy alkaline earth metals on the map Synthetic access, structure evaluation and reactivity studies of heavy alkaline earth organometallics /." Related electronic resource: Current Research at SU : database of SU dissertations, recent titles available full text, 2008. http://wwwlib.umi.com/cr/syr/main.

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Bezougli, Izoldi P. "Insertion reactions of Group 2 metal alkoxides." Thesis, Imperial College London, 1998. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.484172.

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Witherow, Rebecca A. "Minor Alkaline Earth Element and Alkali Metal Behavior in Closed-Basin Lakes." The Ohio State University, 2009. http://rave.ohiolink.edu/etdc/view?acc_num=osu1250628213.

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Caro, Catherine F. "N- and C-centred anionic ligand complexes of the alkaline earth metals." Thesis, University of Sussex, 1998. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.263911.

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Hill, Matthew Roland Chemistry Faculty of Science UNSW. "The single source chemical vapour deposition of alkaline earth metal oxide thin films." Awarded by:University of New South Wales. School of Chemistry, 2006. http://handle.unsw.edu.au/1959.4/32903.

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Metal oxide thin films are dynamic materials that have revolutionised the nature of semiconductor and electronic thin film devices. Recently, progress has stagnated in some aspects due to the increasingly complex deposition apparatus required, and the dearth of suitable precursor complexes of certain ???difficult??? metals. This thesis seeks to address both of these issues. The application of a precursor complex, Mg6(O2CNEt2)12 to the SSCVD of MgO thin films delivered the highest quality films ever reported with this technique. The resultant films were found to be of purely (111) orientation. Due to the nature of the precursor, the chemical reactions occurring at the surface during SSCVD growth result in a high growth rate, low flux environment and films of (111) orientation have been achieved without the amorphous underlayer. This finding has important implications for buffer layers in perovskite thin film devices. The unprecedented precursor chemistry has been used as a basis for the extremely high quality material produced, along with the unusual, yet beneficial structural morphology it possesses. A new range of barium complexes with single encapsulating ligands have been prepared for use in chemical vapour deposition (CVD) of BaTiO3 thin films. A novel pathway to an unprecedented class of barium carbamates is reported, and also new dianionic bis ??-ketoesterates and their barium, strontium, and calcium analogues were synthesised. High resolution mass spectrometry showed the barium bis ??-ketoesterate derivatives to be monomeric, and preliminary testing indicated some volatility in these species. Insights were gained into the likely successful pathways to building a volatile heterobimetallic precursor complex containing an alkaline earth metal. The knowledge of intimate mixing in heterobimetallic precursor complexes was extended by some novel chemistry to develop the first mixed Zn/Mg carbamato cluster complexes. These complexes were found to be excellent SSCVD precursors for ZnxMg1-xO thin films. Thin films were deposited with these precursors and exhibited a single preferred orientation, with a constant amount of magnesium throughout the bulk of the films. Investigation of the light emission properties of the films revealed significant improvements in the structural order commensurate with the incorporation of magnesium, and the formation of the ZnxMg1-xO alloy.
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Al-Terkawi, Abdal-Azim. "Fluorinated and Fluorine-Free Coordination Polymers Based on Alkaline Earth Metals via Mechanochemistry." Doctoral thesis, Humboldt-Universität zu Berlin, 2018. http://dx.doi.org/10.18452/19246.

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Fluorhaltige-Koordinationspolymere (FCPs) wurden durch mechanochemische Reaktionen synthetisiert. Die Erdalkalimetallhydroxide, die in ihrem Wassergehalt variieren, wurden als anorganische Quellen verwendet. Die perfluorierten Benzol Dicarboxylsäuren und ihre fluorfreien Analoga wurden als organische Linker verwendet. Die erhaltenen FCPs werden mit den fluorfreien Verbindungen (CPs) verglichen, die unter den gleichen Mahlbedingungen synthetisiert wurden. Der Austausch von Wasserstoff- durch Fluoratome beeinflusst sowohl die thermischen als auch die strukturellen Eigenschaften der FCPs. Letztere werden auch von den Unterschieden der Geometrien und von der Natur der organischen Linker beeinflusst. Während des Mahlprozesses dient Wasser dabei hauptsächlich als Vermittlermedium und zur Stabilisierung der neuen Strukturen. Die Unterschiede in den Kationengrößen zwischen Ca2+- und Sr2+-Ionen wirken sich geringfügig auf ihre Koordination durch die Dicarboxylatanionen aus. Hier kristallisieren Ca- und Sr-Verbindungen zumeist isomorph. Im Gegensatz dazu beeinflusst der große Ionenradius der Ba2+-Kationen die lokalen Koordinationsumgebungen. Die durch Mahlen erhaltenen Verbindungen sind hydratisiert und weisen eine kleine spezifische Oberfläche auf, die nach der thermischen Behandlung zunehmen kann. Die FCPs sind bis zu 300 °C stabil, während die CPs sich erst oberhalb von 400 °C zersetzen. Die hydratisierten Proben wandeln sich beim Tempern in neue dehydratisierte Phasen um. Die Phasenumwandlung kann reversible ablaufen. Zusätzlich wurde der Effekt des Austausches einer Carboxylgruppe durch eine Aminogruppe in einem organischen Liganden untersucht. In den CPs auf der Basis von Anthranilsäure beeinflussen die unterschiedlichen Kationengrößen der Ca2+-, Sr2+-, und Ba2+-Ionen sowohl die Koordinationsumgebung als auch die Dimensionalität der CPs.Die physikalisch-chemischen Eigenschaften der neuen Materialien wurden systematisch durch verschiedene analytische Techniken.
A series of fluorinated coordination polymers (FCPs) were mechanochemically synthesized using alkaline earth metal hydroxides (M = Ca, Sr, Ba) that vary in their water content as inorganic sources. The perfluorinated benzene-dicarboxylic acids and their fluorine-free analogs were used as organic linkers. The obtained FCPs are compared to their synthesized fluorine-free counterparts (CPs) under the same conditions. The presence of fluorine influences both thermal and structural properties of the resulting FCPs. The latter are also strongly affected by the difference in geometries and nature of organic linkers. Water introduced to grinding acts as a mediator for the milling process and as a reactant for stabilizing the resulting structures. The difference in cation size between Ca2+- and Sr2+-ions has a minor effect on their coordination with perfluorinated or fluorine free benzene-dicarboxylate anions. Here, Ca- and Sr-compounds crystallize isomorphously (an exception was recorded for ortho-phthalate systems). In contrast, the relatively larger size of Ba2+-cation strongly influences the coordination environment. The obtained compounds by milling are hydrated and exhibit small surface areas that can increase after thermal post-treatment. The FCPs are stable up to 300 ˚C. On the other hand, the nonfluorinated CPs begin to decompose above 400 ˚C. The hydrated samples transform into new dehydrated phases upon thermal annealing. The hydrated-dehydrated phase transformation can be reversible. Moreover, the effect of replacement of one carboxylic group by an amino group in an organic ligand was explored. In the CPs based on anthranilic acid, the variations in cation size between Ca2+-, Sr2+-, and Ba2+-ions affect both coordination environment and dimensionality of the resulting CPs. The physicochemical properties of the new materials were systematically investigated applying different analytical techniques.
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Books on the topic "Alkaline earth metals"

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Halka, Monica. Alkali and alkaline earth metals. New York, NY: Facts on File, 2010.

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Brian, Nordstrom, ed. Alkali and alkaline earth metals. New York, NY: Facts on File, 2010.

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Drit͡s, M. E. Splavy shchelochnykh i shchelochnozemelʹnykh metallov: Spravochnik. Moskva: "Metallurgii͡a", 1986.

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Chee-yan, Chan, Khoo Kean H, Lepeshkov I. N, and International Union of Pure and Applied Chemistry., eds. Alkaline earth metal perchlorates. Oxford: Pergamon, 1989.

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Han, Qiyong. Rare earth, alkaline earth and other elements in metallurgy. Tokyo: Japan Technical Information Service, 1998.

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W, Ohse Roland, and International Union of Pure and Applied Chemistry., eds. Handbook of thermodynamic and transport properties of alkali metals. Oxford: Blackwell Scientific, 1985.

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W, Ohse Roland, and International Union of Pure and Applied Chemistry., eds. Handbook of thermodynamic and transport properties of alkali metals. Oxford: Blackwell Scientific, 1985.

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Kuznet︠s︡ova, L. G. (Li︠u︡dmila Georgievna) and Shmakin Boris Matveevich, eds. Geokhimii︠a︡ spodumenovykh pegmatitov i shchelochno-redkometallʹnykh metasomatitiov. Novosibirsk: "Nauka," Sibirskoe otd-nie, 1990.

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G, Walthall Frank, Philpotts John A, and Geological Survey (U.S.), eds. Abundances of Li, Rb, and Sr in W-2, BCR-1, and AC-E determined by isotope dilution mass spectroscopy. [Reston, VA]: U.S. Dept. of the Interior, Geological Survey, 1993.

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Noble, E. G. Solubilities of chloride salts of alkali and alkaline-earth metals when sparged with hydrogen chloride. Pittsburgh, Pa: U.S. Dept. of the Interior, Bureau of Mines, 1985.

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Book chapters on the topic "Alkaline earth metals"

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Arevalo, Ricardo. "Alkali and Alkaline Earth Metals." In Encyclopedia of Earth Sciences Series, 1–4. Cham: Springer International Publishing, 2016. http://dx.doi.org/10.1007/978-3-319-39193-9_211-1.

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Arevalo, Ricardo. "Alkali and Alkaline Earth Metals." In Encyclopedia of Earth Sciences Series, 23–26. Cham: Springer International Publishing, 2018. http://dx.doi.org/10.1007/978-3-319-39312-4_211.

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Roundhill, D. Max. "Alkali and Alkaline Earth Metals." In Extraction of Metals from Soils and Waters, 247–87. Boston, MA: Springer US, 2001. http://dx.doi.org/10.1007/978-1-4757-5204-5_11.

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Borgstedt, Hans Ulrich. "With Alkaline Earth Metals." In U Uranium, 14–81. Berlin, Heidelberg: Springer Berlin Heidelberg, 1989. http://dx.doi.org/10.1007/978-3-662-05671-4_2.

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Papaconstantopoulos, Dimitris A. "The Alkaline Earth Metals." In Handbook of the Band Structure of Elemental Solids, 81–113. Boston, MA: Springer US, 2014. http://dx.doi.org/10.1007/978-1-4419-8264-3_3.

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Akitt, J. W. "The Alkali and Alkaline Earth Metals." In Multinuclear NMR, 189–220. Boston, MA: Springer US, 1987. http://dx.doi.org/10.1007/978-1-4613-1783-8_7.

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Watts, G. R. "Alloys with Alkaline Earth Metals." In Rh Rhodium, 55–57. Berlin, Heidelberg: Springer Berlin Heidelberg, 1991. http://dx.doi.org/10.1007/978-3-662-06411-5_12.

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Tytko, Karl-Heinz, Wolf-Dietrich Fleischmann, Dieter Gras, Eberhard Warkentin, Hartmut Katscher, and Friedrich Schröder. "Molybdate Hydrates with Alkaline Earth Metals." In Mo Molybdenum, 177–213. Berlin, Heidelberg: Springer Berlin Heidelberg, 1985. http://dx.doi.org/10.1007/978-3-662-07836-5_3.

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Meher, S. N., A. K. Rout, and B. K. Padhi. "Extraction of Alumina from Red Mud by Divalent Alkaline Earth Metal Soda Ash Sinter Process." In Light Metals 2011, 231–36. Cham: Springer International Publishing, 2011. http://dx.doi.org/10.1007/978-3-319-48160-9_41.

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Meher, S. N., A. K. Rout, and B. K. Padhi. "Extraction of Alumina from Red Mud by Divalent Alkaline Earth Metal Soda Ash Sinter Process." In Light Metals 2011, 231–36. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2011. http://dx.doi.org/10.1002/9781118061992.ch41.

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Conference papers on the topic "Alkaline earth metals"

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Verdieva, Z. N., I. K. Garkushin, N. N. Verdiev, M. Sh Zeynalov, and P. A. Musaeva. "ENERGY HEAT CARRIERS FROM HALOGENIDES ALKALINE AND ALKALINE EARTH METALS." In RENEWABLE ENERGY: CHALLENGES AND PROSPECTS. ALEF, 2020. http://dx.doi.org/10.33580/2313-5743-2020-8-1-331-339.

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Теоретическими методами рассчитаны температуры плавления и составы эвтектик двух- и трехкомпонентных систем, являющихся элементами малой мерности пятикомпонентной системы сформированной из фторидов и лития, натрия, калия, кальция и бария. Проведен сравнительный анализ теоретически и экспериментально полученных данных с целью определения целесообразности использования расчётных методов. Установлено, что относительная погрешность при определении температур кристаллизации 0,2 -10%, составов нонвариантных точек 0-24,9%. С использованием теории графов произведено разбиение системы на симплексы, сформированы древа фаз и кристаллизаций. Для построения древ использован алгоритм моделирования схем кристаллизации моно-и нонвариантных фазовых равновесий в многокомпонентных системах, правомерность древа фаз подтверждена рентгенофазовым, а температуры кристаллизаций нонвариантных составов выявлены дифференциальным термическим методами физико-химического анализа. Планирование эксперимента осуществлялось проекционно-термографическим методом, опираясь на теоретически рассчитанные эвтектики. Дифференциальным термическим, дифференциальным сканирующим калориметрическим и термогравиметрическим методами физико-химического анализа изучены теплофизические характеристики ряда секущих треугольников четырехкомпонентных систем (квазитройных систем). В результате проведенных исследований выявлены нонвариантные составы и прилегающие к ним области неразделимости термоэффектов при скорости охлаждения 10°С в мин. Все выявленные составы обладают достаточными значениями энтальпий фазовых переходов (кДж/г). и могут быть использованы в качестве теплоносителей и теплонакопителей в устройствах предназначенных для аккумулирования тепла возобновляемых источников энергии. А также полученные эвтектические составы могут быть использованы в качестве электролитов химических источников тока и флюсов при сварке цветных металлов.
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Ekimova, Irina, Tamara Minakova, and Tatyana Ogneva. "Phisicochemistry of alkaline-earth metals oxides surface." In ADVANCED MATERIALS IN TECHNOLOGY AND CONSTRUCTION (AMTC-2015): Proceedings of the II All-Russian Scientific Conference of Young Scientists “Advanced Materials in Technology and Construction”. AIP Publishing LLC, 2016. http://dx.doi.org/10.1063/1.4937869.

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Yamskikh, A. A., and L. A. Ivanova. "Synthesis of chelated compounds of amino acids with metals." In VIII Vserossijskaja konferencija s mezhdunarodnym uchastiem «Mediko-fiziologicheskie problemy jekologii cheloveka». Publishing center of Ulyanovsk State University, 2021. http://dx.doi.org/10.34014/mpphe.2021-251-254.

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The article describes the reactions of glycine synthesis with alkaline, alkaline-earth and divalent 3-d metals, which were carried out during the experiment. Hydroxides or sulfates of lithium, magnesium, calcium, manganese, iron, copper, zinc, cobalt and sodium were used as reagents for the synthesis. The physicochemical properties of the obtained compounds were studied. Keywords: chelates, glycinates of alkaline and alkaline earth metals, glycinates of divalent 3-d metals.
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Thakore, B. Y., P. H. Suthar, S. G. Khambholja, P. N. Gajjar, A. R. Jani, Dinesh K. Aswal, and Anil K. Debnath. "Dynamical Correlation In Some Liquid Alkaline Earth Metals Near Melting." In INTERNATIONAL CONFERENCE ON PHYSICS OF EMERGING FUNCTIONAL MATERIALS (PEFM-2010). AIP, 2010. http://dx.doi.org/10.1063/1.3530458.

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Dvornik, G. P. "QURTZ-EGIRIENE-MICROCLINE METASOMATITES: CONDITIONS BUILDUPS, MINERAGENY." In Проблемы минералогии, петрографии и металлогении. Научные чтения памяти П. Н. Чирвинского. Perm State University, 2023. http://dx.doi.org/10.17072/chirvinsky.2023.20.

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Qurtz-egirine-microcline metasomatites related to independent metasomatic formation. They formed in the conditions display of processes silicon-iron-potassium metasomatism on areas of distribution rocks alkaline-granite and alkaline-syenite series, fenites and microcline-sericite metasomatites. Defined conditions formation and minerageny (precious-metals, rare-metals, rare-earth mineralization) qurtzegirine- microcline metasomatites in the massif of Central Aldan, West Aldan, Urals alkaline province.
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Warner, Nathaniel. "BIOACCUMULATION OF ALKALINE EARTH METALS ASSOCIATED WITH OIL AND GAS OPERATIONS." In 67th Annual Southeastern GSA Section Meeting - 2018. Geological Society of America, 2018. http://dx.doi.org/10.1130/abs/2018se-312905.

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Korkmaz, S. D., Ş Korkmaz, and F. Resuloǧlu. "A Comparative Study of Electrical Resistivity of Liquid Alkaline Earth Metals." In SIXTH INTERNATIONAL CONFERENCE OF THE BALKAN PHYSICAL UNION. AIP, 2007. http://dx.doi.org/10.1063/1.2733390.

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SLÍVA, Aleš, Jaromír DRÁPALA, and Robert BRÁZDA. "Innovation of apparatus for processing metals of loose nature tending to air oxidation, especially alkaline earth metals." In METAL 2019. TANGER Ltd., 2019. http://dx.doi.org/10.37904/metal.2019.929.

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Kazantsev, S. O., and A. S. Lozhkomoev. "Synthesis of nanostructured composites based on alumina oxide and alkaline earth metals." In PROCEEDINGS OF THE INTERNATIONAL CONFERENCE ON PHYSICAL MESOMECHANICS. MATERIALS WITH MULTILEVEL HIERARCHICAL STRUCTURE AND INTELLIGENT MANUFACTURING TECHNOLOGY. AIP Publishing, 2020. http://dx.doi.org/10.1063/5.0034405.

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POZHYVATENKO, V. "Study of the accuracy of first-principle calculations of the properties of chalcogenides of alkaline earth metals." In international scientific-practical conference. MYKOLAYIV NATIONAL AGRARIAN UNIVERSITY, 2024. http://dx.doi.org/10.31521/978-617-7149-78-0-39.

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Reports on the topic "Alkaline earth metals"

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Taylor-Pashow, Kathryn, Thong Hang, and Daniel McCabe. PRELIMINARY DETERMINATION OF THE IMPACT OF ALKALINE EARTH METALS ON CRYSTALLINE SILICOTITANATE. Office of Scientific and Technical Information (OSTI), January 2020. http://dx.doi.org/10.2172/1600709.

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Wang, K., G. S. Chottiner, P. Herrera-Fierro, and D. A. Scherson. Ex-situ and in-situ spectroscopic studies of the passive film on alkali and alkaline earth metals in nonaqueous solvents. Office of Scientific and Technical Information (OSTI), March 1992. http://dx.doi.org/10.2172/7254901.

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Wang, K., G. S. Chottiner, P. Herrera-Fierro, and D. A. Scherson. Ex-situ and in-situ spectroscopic studies of the passive film on alkali and alkaline earth metals in nonaqueous solvents. Final report. Office of Scientific and Technical Information (OSTI), March 1992. http://dx.doi.org/10.2172/10180284.

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Scherson, D., G. Chottiner, P. Herrara-Fierro, and Xuekun Xing. Spectroscopic studies of the passive film on alkali and alkaline earth metals in non-aqueous solvents: A surface science approach: Final report. Office of Scientific and Technical Information (OSTI), October 1987. http://dx.doi.org/10.2172/5554162.

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Chase, M. W. Thermodynamic properties of the alkaline earth metal hydroxides (MOH) I:. Gaithersburg, MD: National Bureau of Standards, 1987. http://dx.doi.org/10.6028/nbs.tn.1243.

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Kim, Hojong, Supathorn Phongikaroon, and James L. Willit. Fundamental Electrochemical Properties of Liquid Metals in LiCl-KCl for Separation of Alkali/Alkaline-Earths (Cs, Sr, and Ba). Office of Scientific and Technical Information (OSTI), December 2018. http://dx.doi.org/10.2172/1490212.

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Dunn, C. E., and N. L. Hastings. Biogeochemical survey of the Fraser Lake area using outer bark of Lodgepole pine (NTS 93K02/03): alkali metals, alkaline earths, manganese and aluminum, central British Columbia. Natural Resources Canada/ESS/Scientific and Technical Publishing Services, 1999. http://dx.doi.org/10.4095/210376.

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Fondeur, F. F. The Effect of Alkaline Earth Metal on the Cesium Loading of Ionsiv(R) IE-910 and IE-911. Office of Scientific and Technical Information (OSTI), January 2001. http://dx.doi.org/10.2172/773568.

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Corriveau, L., and E. G. Potter. Advancing exploration for iron oxide-copper-gold and affiliated deposits in Canada: context, scientific overview, outcomes, and impacts. Natural Resources Canada/CMSS/Information Management, 2024. http://dx.doi.org/10.4095/332495.

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Abstract:
The Geo-mapping for Energy and Minerals (GEM) and Targeted Geoscience Initiative (TGI) programs conducted extensive collaborative research on mineral systems with iron oxide-copper-gold (IOCG) and affiliated deposits in prospective settings of Canada. Regional alteration mapping as well as geochemical and geophysical modelling undertaken under the GEM program documented the evolution of polymetallic metasomatic systems with iron-oxide and alkali-calcic alteration and led to an increased recognition of the mineral potential of poorly explored areas and historic deposits of the Great Bear magmatic zone in the Northwest Territories, thus providing a solid framework for exploration. Early and barren albitite corridors form across the mineral systems and locally host uranium mineralization associated with telescoping of alteration facies by tectonic activity during the metasomatic growth of the systems. Subsequent to albitization, high-temperature Ca-Fe and Ca-K-Fe alteration form iron oxide-apatite (± rare-earth element) mineralization and IOCG variants rich in cobalt and other critical metals, respectively. Systems that further mature to K-Fe alteration form IOCG mineralization and can evolve to mineralized near-surface phyllic alteration and epithermal caps. Transitional facies also host polymetallic skarn mineralization. Rare-earth element enrichments within iron oxide-apatite zones are strongest where remobilization has occurred, particularly along deformation zones. The TGI projects documented the pertinence for a GEM activity in the Great Bear magmatic zone and subsequently synthesized GEM geoscientific data into a system-scale, ore-deposit model, and outlined criteria for mineral resource assessment. This model, and newly developed field-mapping and lithogeochemical tools were shown to be efficient mineral exploration and regional mapping methods in Canada and were also applied to the archetype IOCG deposit, Olympic Dam, and other deposits in the Olympic Cu-Au metallogenic province of Australia. Case examples also include the Romanet Horst in the Trans-Hudson Orogen (second phase of GEM), the Central Mineral Belt in Labrador (TGI), the Wanapitei Lake district in Ontario (private sector exploration results used by TGI), and the Bondy gneiss complex in Quebec (TGI).
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Dunn, C. D., and N. L. Hastings. Biogeochemical survey of the Nechako River area using outer back of Lodgepole pine (NTS 93 F/9, 93 F/10, 93 F/15, 93 F/16 and parts of 93 F/11, 93 F/14, 93 K/1 and 93 K/2), alkali metals, alkaline earths, manganese and aluminum, central British Columbia. Natural Resources Canada/ESS/Scientific and Technical Publishing Services, 2000. http://dx.doi.org/10.4095/211477.

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