Relevant bibliographies by topics / IRON HYDRIDES

Contents

  1. Journal articles
  2. Dissertations / Theses
  3. Books
  4. Book chapters
  5. Conference papers
  6. Reports

Academic literature on the topic 'IRON HYDRIDES'

Author: Grafiati
Published: 4 June 2021
Last updated: 1 February 2022

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Journal articles on the topic "IRON HYDRIDES"

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Serovaiskii, A. Yu, A. Yu Kolesnikov, and V. G. Kutcherov. "Formation of iron hydride and iron carbide from hydrocarbon systems at ultra high thermobaric conditions." Геохимия 64, no. 9 (September 20, 2019): 995–1002. http://dx.doi.org/10.31857/s0016-7525649995-1002.

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The chemical interaction of hydrocarbon systems and iron-bearing minerals was investigated under extreme thermobaric conditions, corresponding to the Earth upper mantle. As a result of the reaction, the formation of iron carbide and iron hydride was detected. The experiments were carried out in diamond anvils cells with laser heating. Natural petroleum from the Korchaginskoe deposit and a synthetic mixture of paraffin hydrocarbons were used as hydrocarbon systems, and pyroxene-like glass and ferropericlase (57Fe enriched) as iron bearing minerals. The experiments were carried out in the pressure range of 26–95 kbar and temperature range of 1000–1500°C (±100°C). As a result of the experiments, the formation of iron hydride was detected at pressure of 26–69 kbar (corresponds to a depth of 100–200 km), and a mixture of iron carbide and iron hydride at pressure of 75–95 kbar (corresponds to a depth of 210–290 km). The formation of hydrides and iron carbides as a results of the interaction of hydrocarbon systems with iron-bearing minerals may indicate the possible existence of these compounds in the upper mantle.
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Dufour, Jacques, Xavier Dufour, Fabienne Dioury, and Jenny D. Vinko. "Measurement of the enthalpy of formation of an iron pico-hydride and of its main properties." International Journal of Modern Physics B 31, no. 25 (October 10, 2017): 1745007. http://dx.doi.org/10.1142/s0217979217450072.

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Chemical reactions result from the outside shell electrons of the reacting species being shared in various types of combinations. Typical distances involved are tenths of nm, resulting in binding energies typically in the order of hundreds of kJ/mole (eV/atom). The synthesis of a novel “atomic system” formed from Iron and di-Hydrogen has been achieved. The measured enthalpy of formation is some 40 MJ/moleFe and the distance between the hydrogen proton and the iron nucleus is some 8 pm, hence the proposed name: Iron Pico-Hydride. This compound is a permanent electric dipole of atomic size. Pico-Hydrides could, thus, play a significant role in HT superconductivity and in super-capacitors. The synthesis is compatible with the standard model.
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Haim, Lorraine, François Robert, Laurent Peres, Pierre Lecante, Karine Philippot, Romuald Poteau, Marc Respaud, and Catherine Amiens. "Correlation between surface chemistry and magnetism in iron nanoparticles." Nanoscale Advances 3, no. 15 (2021): 4471–81. http://dx.doi.org/10.1039/d1na00258a.

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Morris, Robert H. "Iron Group Hydrides in Noyori Bifunctional Catalysis." Chemical Record 16, no. 6 (August 15, 2016): 2644–58. http://dx.doi.org/10.1002/tcr.201600080.

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Antonov, V. E., M. Baier, B. Dorner, V. K. Fedotov, G. Grosse, A. I. Kolesnikov, E. G. Ponyatovsky, G. Schneider, and F. E. Wagner. "High-pressure hydrides of iron and its alloys." Journal of Physics: Condensed Matter 14, no. 25 (June 13, 2002): 6427–45. http://dx.doi.org/10.1088/0953-8984/14/25/311.

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Liu, Jianguo, Ailing Zhang, Heng Song, Qingxiao Tong, Chen-Ho Tung, and Wenguang Wang. "Iron(II) hydrides bearing a tetradentate PSNP ligand." Chinese Chemical Letters 29, no. 6 (June 2018): 949–53. http://dx.doi.org/10.1016/j.cclet.2017.09.059.

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Gee, Leland B., Vladimir Pelmenschikov, Hongxin Wang, Nakul Mishra, Yu-Chiao Liu, Yoshitaka Yoda, Kenji Tamasaku, Ming-Hsi Chiang, and Stephen P. Cramer. "Vibrational characterization of a diiron bridging hydride complex – a model for hydrogen catalysis." Chemical Science 11, no. 21 (2020): 5487–93. http://dx.doi.org/10.1039/d0sc01290d.

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Kiernicki, John J., James P. Shanahan, Matthias Zeller, and Nathaniel K. Szymczak. "Tuning ligand field strength with pendent Lewis acids: access to high spin iron hydrides." Chemical Science 10, no. 21 (2019): 5539–45. http://dx.doi.org/10.1039/c9sc00561g.

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Pendent borane Lewis acids provide an avenue for changing a ligand's field strength through acid/base interactions; this strategy was highlighted within a series of biologically-relevant high spin iron hydrides.
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Chang, Guoliang, Peng Zhang, Wenjing Yang, Shangqing Xie, Hongjian Sun, Xiaoyan Li, Olaf Fuhr, and Dieter Fenske. "Correction: Pyridine N-oxide promoted hydrosilylation of carbonyl compounds catalyzed by [PSiP]-pincer iron hydrides." Dalton Transactions 49, no. 32 (2020): 11412. http://dx.doi.org/10.1039/d0dt90147d.

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Correction for ‘Pyridine N-oxide promoted hydrosilylation of carbonyl compounds catalyzed by [PSiP]-pincer iron hydrides’ by Guoliang Chang et al., Dalton Trans., 2020, 49, 9349–9354, DOI: 10.1039/D0DT00392A.
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Chang, Guoliang, Peng Zhang, Wenjing Yang, Shangqing Xie, Hongjian Sun, Xiaoyan Li, Olaf Fuhr, and Dieter Fenske. "Pyridine N-oxide promoted hydrosilylation of carbonyl compounds catalyzed by [PSiP]-pincer iron hydrides." Dalton Transactions 49, no. 27 (2020): 9349–54. http://dx.doi.org/10.1039/d0dt00392a.

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Five [PSiP]-pincer iron hydrides 1–5 were used as catalysts to study the effects of pyridine N-oxide and the electronic properties of [PSiP]-ligands on the catalytic hydrosilylation of carbonyl compounds.
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Dissertations / Theses on the topic "IRON HYDRIDES"

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Helleren, Caroline Anne. "A search for bridging-dinitrogen heterobimetallic complexes containing iron and molybdenum or tungsten." Thesis, University of Sussex, 1998. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.241719.

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Hullah, Daniel Fearnley. "The electronic spectra of FeH and TeO←2." Thesis, University of Oxford, 1999. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.301915.

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FALCAO, RAILSON B. "Síntese por reação do TiFe nanoestruturado para o armazenamento de hidrogênio, a partir da moagem de alta energia de misturas de pós de TiH2 e Fe." reponame:Repositório Institucional do IPEN, 2016. http://repositorio.ipen.br:8080/xmlui/handle/123456789/27135.

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Neste trabalho investigou-se a obtenção do composto TiFe a partir da moagem de alta energia de misturas de pós de TiH2 e Fe, seguida de aquecimento sob vácuo para a reação de síntese. No lugar do Ti, o TiH2 foi escolhido como precursor em razão de sua fragilidade, benéfica para a diminuição da aderência dos pós ao ferramental de moagem. Foram preparados dois lotes de misturas obedecendo-se a relação Ti:Fe de 50:50 e 56:44. Ambos foram processados em um moinho do tipo planetário por tempos que variaram de 5 até 40 horas, sob atmosfera de argônio de elevada pureza. Em todos os experimentos foram mantidos constantes a velocidade de rotação do prato do moinho, a quantidade de amostra, o diâmetro e o número de bolas. As amostras moídas foram caracterizadas por calorimetria exploratória diferencial (DSC), termogravimetria (TG), microscopia eletrônica de varredura (MEV), difração de raios X (DRX) e fluorescência de raios X por dispersão de energia (EDXRF). Apenas TiH2 e Fe foram observados nas amostras moídas, com um grau crescente de mistura em função do tempo de moagem. O composto TiFe nanoestruturado (12,5 a 21,4nm) foi obtido de forma majoritária em todas as amostras após a reação de síntese promovida pelo tratamento térmico a 600ºC (873K). As amostras reagidas foram caracterizadas por microscopia eletrônica de transmissão (MET) e DRX. Um equipamento do tipo Sievert, operando sob um fluxo constante (modo dinâmico), foi utilizado para levantar as curvas termodinâmicas de absorção e dessorção de hidrogênio. Todas as amostras absorveram hidrogênio à temperatura ambiente (~298K) sem a necessidade de ciclos térmicos de ativação. Os melhores resultados foram obtidos com as amostras moídas por 25 e 40 horas, de composição não estequiométrica 56:44. Tais amostras absorveram e dessorveram hidrogênio à temperatura ambiente, sob os platôs de aproximadamente 6,4 e 2,2bar (~0,6 e 0,2MPa), respectivamente. A capacidade máxima de armazenamento foi de 1,06% em massa de hidrogênio (H:M~0,546), sob pressão de até 11bar (1,1MPa), com reversão de até 1,085% em massa de hidrogênio (H:M~0,559), sob pressão de até 1bar (0,1MPa). Estas amostras também apresentaram maior cinética de absorção e dessorção de hidrogênio com fluxos de 1,23 (25h) e 2,86cm3/g.min. (40h). Tais resultados são atribuídos à variação composicional da fase TiFe e à maior quantidade de TiH2 livre.
Tese (Doutorado em Tecnologia Nuclear )
IPEN/D
Instituto de Pesquisas Energéticas e Nucleares - IPEN-CNEN/SP
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GALEGO, EGUIBERTO. "Estudo de ligas e imás preparados pelo processo hidrogenação, desproporção, dessorção e recombinação (HDDR) a base de Pr-Fe-B com adição de dopantes e elementos de liga." reponame:Repositório Institucional do IPEN, 2008. http://repositorio.ipen.br:8080/xmlui/handle/123456789/11611.

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Tese (Doutoramento)
IPEN/T
Instituto de Pesquisas Energéticas e Nucleares - IPEN-CNEN/SP
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Zhu, Kailong. "Iron-catalysed hydride and radical transfer reactions." Thesis, University of Edinburgh, 2017. http://hdl.handle.net/1842/28732.

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Iron-catalysed carbonyl reduction, nitro reduction, formal hydroamination, and the radical alkenylation of alkyl halides have been developed. A Simple, easy-to-make, air- and moisture-stable iron(III) amine-bis(phenolate) complex catalysed the hydrosilylation of carbonyl compounds efficiently using triethoxysilane as the reducing agent. The reaction tolerated a wide range of substrates to give the corresponding alcohol products in good to excellent yields after hydrolysis of the hydrosilylated products (Scheme A1). Scheme A1. Iron-Catalysed Hydrosilylation of Carbonyl Compounds. The same catalyst was also an active catalyst for the chemoselective reduction of nitro arenes into corresponding amines using triethoxysilane as reducing agent. The method exhibited excellent chemoselectivity as other reducible functional groups such as halogen, ester, nitrile all kept unchanged during the reaction. This catalytic system was then successfully applied to the formal hydroamination of alkene to give substituted amine in synthetic useful yields under mild condition. The reaction is hypothesised to proceed through a radical intermediate (Scheme A2). Scheme A2. Iron-Catalysed Nitro Reduction and Alkene Formal Hydroamination. Finally, FeCl2-catalysed formal Heck cross-coupling has been developed between alkyl halides and styrenes. The reaction tolerated both electron-rich and electron-neutral substrates to give the products in moderate to excellent yields. Initial studies revealed that the reaction also proceeds through a radical intermediate (Scheme A3). Scheme A3. Iron-Catalysed Formal Heck Cross-Coupling of Functionalised Alkyl Halides.
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Wilson, Catherine. "Further analysis of the electronic spectrum of FeH." Thesis, University of Oxford, 2001. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.365782.

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Lavender, Mark Harley. "Phosphine stabilised di-iron complexes." Thesis, University College London (University of London), 1995. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.283749.

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Older, Jamie Edward John. "Asymmetric induction of n4-iron diene complexes." Thesis, University of East Anglia, 2001. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.368217.

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The use of tricarbonyliron chemistry in asymmetric synthesis is of increasing importance. With this comes the need for efficient and reliable techniques for the production of enantiopure starting materials. The methods currently available, although effective, are often long winded and wasteful. The development of a chiral hydride abstraction reagent analogous to the triphenylcarbenium species would be of great value in terms of improved yields and simplification of strategy. This thesis details the development of a system based around the dibenzosuberane frame-work. Two different chiral biases have been introduced to the structure leading to a potential double stereodifferentiation effect. Substitution of the 'backbone' of the structure has yielded enantiomeric excesses of up to 54%. The smaller, chiral aryl bias has given e.e.s in the region of 10%. Moreover the synthetic route to the backbone substituted examples has been greatly improved and is now suitable for use on a multigram scale.
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Goodridge, Damian Mark. "The green and red systems of the FeH radical." Thesis, University of Oxford, 1997. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.339345.

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Ghostine, Karine. "Reactivity of Low-Valent Iron and Cobalt Complexes with Fluoroalkenes." Thesis, Université d'Ottawa / University of Ottawa, 2018. http://hdl.handle.net/10393/38558.

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Fluorocarbons are versatile molecules that are used in multiple industries ranging from pharmaceuticals to refrigerants, insecticides and advanced materials. More particularly hydrofluorocarbons (HFCs) and hydrofluoroolefins (HFOs) are current replacements for ozone-depleting chlorofluorocarbons (CFCs) that were used for decades as refrigerants, propellants, solvents and blowing agents. However, syntheses of HFCs and HFOs involve energy-intensive processes and toxic compounds such as heavy metals and anhydrous HF. Development of more sustainable, energy efficient and "greener" synthesis of small fluorocarbons is needed, which draws attention to organometallic catalysis, especially with abundant, inexpensive and non-toxic transition metals. One approach to new organometallic routes to hydrofluorocarbons involves the formation and functionalization of fluorometallacycles. Previous work in the 1990’s by Baker et al. demonstrated the catalytic hydrodimerization of tetrafluoroethylene (TFE) using Ni catalysts with π-acidic phosphite ligands. They also demonstrated the hydrogenolysis of the d6 ferracyclopentane, Fe(CO)4(1,4-C4F8), 2-1, under high pressure and temperature with different additives to give mixtures of different hydrofluorocarbons. Since that time the reactivity of d8 fluorometallacyles has been extensively studied, leading to fundamental understanding and new catalytic applications. However less attention has been paid to d6 systems, the synthesis and reactivity of which are the focus of this Thesis. Following introduction and background in Chapter 1, Chapter 2 presents the synthesis and characterization of a series of new NHC-, phosphine- and nitrogen-ligand-substituted Fe(II) perfluorometallacycles derived from complex 2-1. This led to the discovery of the first example of a fluorinated metallacyclocarbene obtained from in situ Cα–F bond activation that afforded FeF(triphos)(1,4-C4F7), 2-6, (triphos = bis(2-diphenylphosphinoethyl)phenylphosphine) during the P-based linear tridentate ligand substitution reaction. [Fe(triphos)(1,4-C4F7)(NCMe)]+BPh4-, 2-7, and Fe(OTf)(triphos)(1,4-C4F7), 2-8, were derived from 2-6 by treatment with NaBPh4 in acetonitrile and Me3Si-OTf, respectively (Tf = triflate, SO2CF3). The same phenomenon was not observed with hard-donor N-based linear tridentate ligand, terpy’, (terpy’ = 4′-(4-methylphenyl)-2,2′:6′,2′′-terpyridine), presumably because of the less Lewis acidic metal center. Fluoride abstraction from Fe(terpy’)(CO)(1,4-C4F8), 2-9, by a Lewis acid, however allowed for Cα–F bond activation to give the cationic iron monocarbonyl carbene complex, [Fe(terpy’)(CO)(1,4-C4F7)]+OTf–, 2-10. Chapter 3 investigates further the reactivity of these new Fe(II) perfluorometallacycle complexes. The lack of reactivity of the mono- and di-substituted Fe carbonyl perfluorometallacycles with Lewis acids confirmed that Cα–F bond activation only occurs when there is enough π-backbonding into the Cα–F anti-bonding orbital, as π-acceptor phosphines and carbonyl ligands can compete for the metal back-bonding. Indeed, Cα–F abstraction is only observed with Fe(terpy’)(CO)(1,4-C4F8), 2-9, due to the poor acceptor ability of the nitrogen ligand. On the other hand, the lack of electron density on the metal center can cause the Fe center to act as an internal Lewis acid, promoting Cα–F migration as observed in situ during the triphos substitution reaction. These results show that d6 [Fe] perfluorometallacycles do not share similar reactivity with d8 [Ni] perfluorometallacycles. Moreover, the study of the character of the Fe=CF bonds suggests a nucleophilic carbene for 2-6, while 2-7, 2-8 and 2-10 all displayed electrophilic carbene character. Furthermore, hydrogenolysis of Fe(OTf)(triphos)(1,4-C4F7), 2-8, and [Fe(triphos)(1,4-C4F7)(NCMe)]+BPh4-, 2-7, at low pressure and room temperature, generated exclusively H(CF2)3CFH2, HFC-347pcc, and iron hydrides, confirming a previous hypothesis that attributed formation of this hydrofluoroalkane to an Fe carbene intermediate. In contrast, [Fe(terpy’)(CO)(1,4-C4F7)]+OTf–, 2-10, reacts with H2 to yield HF and an unidentified iron complex, showing that the nature of the ancillary ligands greatly influences the reactivity. Chapter 4 explores the reactivity of phosphine-substituted cobalt(I) carbonyl hydride complexes towards TFE to expand our work on d6 perfluorometallacycles. The most electron-rich ligands prevented metallacycle formation or slowed it down possibly due to strong π-backbonding into the CO ligands, making it harder to generate an open coordination site. Indeed, a mixture of the Co-tetrafluoroethyl complex, derived from insertion of TFE into Co–H, and the zerovalent dimer/hydrogenated TFE products, derived from the reaction of the Co–H with the 16e- CoLn(CO)3-n(CF2CF2H) intermediate, were obtained with the bulkiest ligands, CoH(dcppe)(CO)2 and CoH(Pcp3)(CO)3 (dcppe = 1,2-bis(dicyclopentylphosphino)ethane, cp = cyclopentyl). With the slightly less bulky PiBu3 ligand, further reactivity of the insertion product with TFE slowly formed a d6 metallacycle hydride complex. In contrast, with the dppe and tripod cobalt carbonyl hydrides, metallacycle product formation was evident even at short reaction times with insertion/hydrogenation ratios of 1:1, showing that using less electron-rich, steric bulky ligands prevented the bimolecular Co dimer formation, but left enough room for binding a second equivalent of TFE for metallacycle formation. Finally, Chapter 5 summarizes the findings of this Thesis and discusses future directions based on this work.
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Books on the topic "IRON HYDRIDES"

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Cappellani, Paul E. The acid-base properties of iron hydride complexes. Ottawa: National Library of Canada, 1990.

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Book chapters on the topic "IRON HYDRIDES"

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Sokolov, V. M. "The Technological Aspects of the Nickel — Iron Accumulator Batteries Recycling." In Hydrogen Materials Science and Chemistry of Metal Hydrides, 71–74. Dordrecht: Springer Netherlands, 2002. http://dx.doi.org/10.1007/978-94-010-0558-6_8.

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Reilly, J. J., and G. Sandrock. "Iron Titanium Hydride (FeTih1.94)." In Inorganic Syntheses, 90–96. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2007. http://dx.doi.org/10.1002/9780470132531.ch18.

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Chevalier, B., J. Etourneau, and J. M. D. Coey. "Structural and Magnetic Properties of RE2Fe17Hx (RE = Nd,Sm) Hydrides and Iron-Rich Compounds Nd(Co1-xFex)9Si2 and Gd(FexAl1-x)12." In Concerted European Action on Magnets (CEAM), 134–45. Dordrecht: Springer Netherlands, 1989. http://dx.doi.org/10.1007/978-94-009-1135-2_11.

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Arndt, Larry W., Christopher J. Bischoff, Marcetta Y. Darensbourg, and John E. Ellis. "Heterobinuclear Nonacarbonyl Complexes and Hydride Complexes of Iron-Chromium, Iron-Molybdenum, and Iron-Tungsten." In Inorganic Syntheses, 335–41. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2007. http://dx.doi.org/10.1002/9780470132579.ch61.

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Peet, W. G., D. H. Gerlach, and D. D. Titus. "Hydride Complexes of Iron(II) and Ruthenium(II)." In Inorganic Syntheses, 38–42. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2007. http://dx.doi.org/10.1002/9780470132463.ch11.

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Pardasani, R. T., and P. Pardasani. "Magnetic properties of 17-electron iron(III) hydride radical cation." In Magnetic Properties of Paramagnetic Compounds, 51–52. Berlin, Heidelberg: Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-662-53971-2_20.

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Pardasani, R. T., and P. Pardasani. "Magnetic properties of half-sandwich hydride complex of iron containing 1, 2-bis(diisopropylphosphino)ethane." In Magnetic Properties of Paramagnetic Compounds, 58. Berlin, Heidelberg: Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-662-53971-2_24.

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Badding, J. V., H. K. Mao, and R. J. Hemley. "High-Pressure Crystal Structure and Equation of State of Iron Hydride: Implications for the Earth's Core." In High-Pressure Research: Application to Earth and Planetary Sciences, 363–71. Washington, D. C.: American Geophysical Union, 2013. http://dx.doi.org/10.1029/gm067p0363.

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Drabowicz, J., D. Krasowska, and J. Wicha. "Using Nickel, Cobalt, Iron, or Copper Compounds and Metal Hydrides." In Alkanes, 1. Georg Thieme Verlag KG, 2009. http://dx.doi.org/10.1055/sos-sd-048-00131.

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Saito, S. "Lithium Aluminum Hydride with Iron Compounds." In Compounds of Groups 13 and 2 (Al, Ga, In, Tl, Be...Ba), 1. Georg Thieme Verlag KG, 2004. http://dx.doi.org/10.1055/sos-sd-007-00036.

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Conference papers on the topic "IRON HYDRIDES"

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Rebak, Raul B., and Young-Jin Kim. "Hydrogen Diffusion in FeCrAl Alloys for Light Water Reactors Cladding Applications." In ASME 2016 Pressure Vessels and Piping Conference. American Society of Mechanical Engineers, 2016. http://dx.doi.org/10.1115/pvp2016-63164.

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There is a worldwide effort to develop nuclear fuels that are resistant to accidents such as loss of coolant in the reactor and the storage pools. In the United States, the Department of Energy is teaming with fuel vendors to develop accident tolerant fuels (ATF), which will resist the lack of cooling for longer periods of times than the current zirconium alloy - uranium dioxide system. General Electric (GE) and its partners is proposing to replace zirconium alloys cladding with an Iron-Chromium-Aluminum (FeCrAl) alloy such as APMT, since they are highly resistant to attack by steam up to the melting point of the alloy. FeCrAl alloys do not react with hydrogen to form stable hydrides as zirconium alloys do. Therefore, it is possible that more tritium may be released to the coolant with the use of FeCrAl cladding. This work discusses the formation of an alumina layer on the surface of APMT cladding as an effective barrier for tritium permeation from the fuel to the coolant across the cladding wall.
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Yagi, T., T. Hishinuma, M. Yamakata, T. Uchida, W. Utsumi, and Y. Fukai. "Formation and structure of iron hydride under the condition of the Earth’s interior." In High-pressure science and technology—1993. AIP, 1994. http://dx.doi.org/10.1063/1.46190.

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Yamakata, Masaaki, Takehiko Yagi, Wataru Utsumi, and Yuh Fukai. "Electrical conductivity and crystal structure of iron hydride under high pressure and high temperature." In High-pressure science and technology—1993. AIP, 1994. http://dx.doi.org/10.1063/1.46192.

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Reports on the topic "IRON HYDRIDES"

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Jackson, Cynthia R. Thermodynamic properties of halides, hydrides, and deuterides of cobalt, iron, and nickel :. Gaithersburg, MD: National Bureau of Standards, 1987. http://dx.doi.org/10.6028/nbs.tn.1244.

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