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Wyszukujesz frazę "crystal structures" wg kryterium: Temat


Wyświetlanie 1-3 z 3
Tytuł:
Comparison study of crystal and electronic structures for chalcopyrite $(CuFeS_2)$ and pyrite $(FeS_2)$
Autorzy:
Li, Yuqiong
Liu, Yingchao
Chen, Jianhua
Zhao, Cuihua
Cui, Weiyong
Powiązania:
https://bibliotekanauki.pl/articles/1448811.pdf
Data publikacji:
2021
Wydawca:
Politechnika Wrocławska. Oficyna Wydawnicza Politechniki Wrocławskiej
Tematy:
chalcopyrite
pyrite
crystal structures
electronic structures
Opis:
Chalcopyrite $(CuFeS_2)$ and pyrite $(FeS_2)$ are commonly associated with each other, and they both belong to semiconductor minerals. The difference in crystal and electronic structures is an important factor for their flotation separation. Using the density functional method (DFT) combined with Hubbard U correction, their crystal and electronic properties are comparatively studied. The calculated results suggest that the use of antiferromagnetic calculations and Hubbard U correction are very important to the accuracy of the chalcopyrite results. Antiferromagnetic calculations combined with a U value of 2.0 eV on chalcopyrite show a band gap of 0.53 eV, which is very consistent with the experimental results of ~0.5 eV. The density of states (DOS) and Mulliken bond population results indicate that stronger hybridization between Fe 3d and S 3p states in chalcopyrite than in pyrite leads to a stronger covalency of Fe-S bonds in chalcopyrite, causing a reduction in the spin magnetic moment (3.5 μB) from the ideal value. In addition, the greater covalency of bonds in chalcopyrite results in greater hydrophobicity of chalcopyrite than pyrite. The DOS results suggest that S has similar electronic properties in pyrite and chalcopyrite. The oxidation states of Fe and Cu ions in chalcopyrite are discussed based on the coordination field theory according to the calculation results, which confirms an oxidation state of $Fe^{3+}Cu^{1+}S_2$.
Źródło:
Physicochemical Problems of Mineral Processing; 2021, 57, 1; 100-111
1643-1049
2084-4735
Pojawia się w:
Physicochemical Problems of Mineral Processing
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Highly Energetic Salts of 3,6-Bishydrazino-1,2,4,5-tetrazine
Autorzy:
Klapötke, T. M.
Preimesser, A.
Schedlbauer, S.
Stierstorfer, J.
Powiązania:
https://bibliotekanauki.pl/articles/358026.pdf
Data publikacji:
2013
Wydawca:
Sieć Badawcza Łukasiewicz - Instytut Przemysłu Organicznego
Tematy:
1,2,4,5-tetrazine
energetic materials
explosives
sensitivities
crystal structures
Opis:
3,6-Bishydrazino-1,2,4,5-tetrazine was synthesized as described by hydrazinolysis of 3,6-bis-(3,5-dimethylpyrazolyl)-1,2,4,5-tetrazine. Doubly protonated 1:1 and 1:2 salts of the highly energetic anions were synthesized. These are bishydrazinium-tetrazine dichloride dihydrate (1:2) (BHT-2HCl•2H2O) (2), bishydrazinium-tetrazine (5,5´-azotetrazolate) dihydrate (1:1) (BHT-ATz•2H2O) (3), bishydrazinium-tetrazine bis (3,5-dinitrotriazolate) dihydrate (1:2) (BHT(DNT)2•2H2O) (4), bishydrazinium-tetrazine bis (5-nitrotetrazolate) (1:2) (BHT(NT)2) (5), bishydrazinium-tetrazine (5,5´-bistetrazolate) dihydrate (1:1) (BHTBT•2H2O) (6), bishydrazinium-tetrazine bistetrazolylamine (1:1) (BHT-BTA) (7), bishydrazinium-tetrazine bis (3-amino-5-nitrotriazolate) (1:2) (BHT-(ANTA)2) (8) and bishydrazinium-tetrazine 4,4´,5,5´-tetranitro-2,2´-bisimidazolate (1:1) (9). Compounds 2-6 could be characterized by low temperature X-ray diffraction. All of the compounds were suffciently analyzed by 1H and {1H}13C and 14N NMR spectroscopy, elemental analysis (CHN), mass spectroscopy (FAB)) and vibrational spectroscopy (IR and Raman). The detonation parameters of the most promising candidates 5 and 9 in terms of energetic applications were calculated using the EXPLO5 V5.05 computer code. The energies of formation were calculated using CBS-4M electronic enthalpies and the atomization method. Furthermore, since all of the compounds are energetic materials, sensitivity tests towards impact (IS), friction (FS) and electrostatical discharge (ESD) were carried out. In addition their thermal stabilities were determined using a differential scanning calorimeter with a heating rate of 5 °C min-1.
Źródło:
Central European Journal of Energetic Materials; 2013, 10, 2; 151-170
1733-7178
Pojawia się w:
Central European Journal of Energetic Materials
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Study on Synthesis and Modification of Conical Ni Structures by One-Step Method
Autorzy:
Skibińska, K.
Semeniuk, S.
Kutyła, D.
Kołczyk-Siedlecka, K.
Jędraczka, A.
Żabiński, P.
Powiązania:
https://bibliotekanauki.pl/articles/2049399.pdf
Data publikacji:
2021
Wydawca:
Polska Akademia Nauk. Czytelnia Czasopism PAN
Tematy:
electrodeposition
one-step method
crystal modifier
nickel cones
free-standing structures
Opis:
In this work the conical Ni structures were obtained from an electrolyte containing NH4Cl as a crystal modifier. This process is called one-step method and allows to cover large areas with micro- and nanostructures during a single electrodeposition. Presence of NH4Cl promotes a vertical direction of structure growth in order to block a horizontal one. Additionally, this method does not require using chromic acid solution, which is dangerous for the environment. Due to the ferromagnetic properties of Ni, obtained coatings could be applied as magnetic devices. The influence of the parameters such as a preparation of copper substrate, a composition of electrolyte and electrodeposition conditions (time, the electrolyte temperature and current density) was investigated in this work.
Źródło:
Archives of Metallurgy and Materials; 2021, 66, 3; 861-869
1733-3490
Pojawia się w:
Archives of Metallurgy and Materials
Dostawca treści:
Biblioteka Nauki
Artykuł
    Wyświetlanie 1-3 z 3

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