Lattice anisotropy in uranium ternary compounds: UTX

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Standard

Lattice anisotropy in uranium ternary compounds : UTX. / Maskova, S.; Adamska, A.M.; Havela, L.; Kim-Ngan, NTH ; Przewoznik, J.; Danis, S.; Kothapalli, K.; Kolomiets, A.V. ; Heathman, S.; Nakotte, H.; Bordallo, Heloisa N.

I: Journal of Alloys and Compounds, Bind 522, 05.05.2012, s. 130-135.

Publikation: Bidrag til tidsskriftTidsskriftartikelfagfællebedømt

Harvard

Maskova, S, Adamska, AM, Havela, L, Kim-Ngan, NTH, Przewoznik, J, Danis, S, Kothapalli, K, Kolomiets, AV, Heathman, S, Nakotte, H & Bordallo, HN 2012, 'Lattice anisotropy in uranium ternary compounds: UTX', Journal of Alloys and Compounds, bind 522, s. 130-135. https://doi.org/10.1016/j.jallcom.2012.01.122

APA

Maskova, S., Adamska, A. M., Havela, L., Kim-Ngan, NTH., Przewoznik, J., Danis, S., Kothapalli, K., Kolomiets, A. V., Heathman, S., Nakotte, H., & Bordallo, H. N. (2012). Lattice anisotropy in uranium ternary compounds: UTX. Journal of Alloys and Compounds, 522, 130-135. https://doi.org/10.1016/j.jallcom.2012.01.122

Vancouver

Maskova S, Adamska AM, Havela L, Kim-Ngan NTH, Przewoznik J, Danis S o.a. Lattice anisotropy in uranium ternary compounds: UTX. Journal of Alloys and Compounds. 2012 maj 5;522:130-135. https://doi.org/10.1016/j.jallcom.2012.01.122

Author

Maskova, S. ; Adamska, A.M. ; Havela, L. ; Kim-Ngan, NTH ; Przewoznik, J. ; Danis, S. ; Kothapalli, K. ; Kolomiets, A.V. ; Heathman, S. ; Nakotte, H. ; Bordallo, Heloisa N. / Lattice anisotropy in uranium ternary compounds : UTX. I: Journal of Alloys and Compounds. 2012 ; Bind 522. s. 130-135.

Bibtex

@article{7033d37c68254fb1a9a5567043e5c7f1,
title = "Lattice anisotropy in uranium ternary compounds: UTX",
abstract = "Several U-based intermetallic compounds (UCoGe, UNiGe with the TiNiSi structure type and UNiAl with the ZrNiAl structure type) and their hydrides were studied from the point of view of compressibility and thermal expansion. Confronted with existing data for the compounds with the ZrNiAl structure type a common pattern emerges. The direction of the U-U bonds with participation of the 5f states is distinctly the {"}soft{"} crystallographic direction, exhibiting also the highest coefficient of linear thermal expansion. The finding leads to an apparent paradox: the closer the U atoms are together in a particular direction the better they can be additionally compressed together by applied hydrostatic pressure. ",
author = "S. Maskova and A.M. Adamska and L. Havela and NTH Kim-Ngan and J. Przewoznik and S. Danis and K. Kothapalli and A.V. Kolomiets and S. Heathman and H. Nakotte and Bordallo, {Heloisa N.}",
year = "2012",
month = may,
day = "5",
doi = "10.1016/j.jallcom.2012.01.122",
language = "English",
volume = "522",
pages = "130--135",
journal = "Journal of Alloys and Compounds",
issn = "0925-8388",
publisher = "Elsevier",

}

RIS

TY - JOUR

T1 - Lattice anisotropy in uranium ternary compounds

T2 - UTX

AU - Maskova, S.

AU - Adamska, A.M.

AU - Havela, L.

AU - Kim-Ngan, NTH

AU - Przewoznik, J.

AU - Danis, S.

AU - Kothapalli, K.

AU - Kolomiets, A.V.

AU - Heathman, S.

AU - Nakotte, H.

AU - Bordallo, Heloisa N.

PY - 2012/5/5

Y1 - 2012/5/5

N2 - Several U-based intermetallic compounds (UCoGe, UNiGe with the TiNiSi structure type and UNiAl with the ZrNiAl structure type) and their hydrides were studied from the point of view of compressibility and thermal expansion. Confronted with existing data for the compounds with the ZrNiAl structure type a common pattern emerges. The direction of the U-U bonds with participation of the 5f states is distinctly the "soft" crystallographic direction, exhibiting also the highest coefficient of linear thermal expansion. The finding leads to an apparent paradox: the closer the U atoms are together in a particular direction the better they can be additionally compressed together by applied hydrostatic pressure.

AB - Several U-based intermetallic compounds (UCoGe, UNiGe with the TiNiSi structure type and UNiAl with the ZrNiAl structure type) and their hydrides were studied from the point of view of compressibility and thermal expansion. Confronted with existing data for the compounds with the ZrNiAl structure type a common pattern emerges. The direction of the U-U bonds with participation of the 5f states is distinctly the "soft" crystallographic direction, exhibiting also the highest coefficient of linear thermal expansion. The finding leads to an apparent paradox: the closer the U atoms are together in a particular direction the better they can be additionally compressed together by applied hydrostatic pressure.

U2 - 10.1016/j.jallcom.2012.01.122

DO - 10.1016/j.jallcom.2012.01.122

M3 - Journal article

VL - 522

SP - 130

EP - 135

JO - Journal of Alloys and Compounds

JF - Journal of Alloys and Compounds

SN - 0925-8388

ER -

ID: 38006163