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Wyświetlanie 1-3 z 3
Tytuł:
Ferrite Decarburization of High Silicon Spring Steel in Three Temperature Ranges
Autorzy:
Zhao, F.
Zhang, C. L.
Liu, Y. Z.
Powiązania:
https://bibliotekanauki.pl/articles/350822.pdf
Data publikacji:
2016
Wydawca:
Polska Akademia Nauk. Czytelnia Czasopism PAN
Tematy:
surface decarburization
steel
oxidation
carbon diffusion
Opis:
Surface decarburization of high silicon spring steel in ambient air was studied. The experimental results confirmed the decarburized mechanism under AC1 temperature, in the temperature range of AC1-AC3 and AC3-G. Under AC1 temperature, pearlite spheroidization and surface decarburization are carried out simultaneously and pearlite spheroidization is reinforced. Considering the oxidation loss depth, the “true ferrite decarburized depth” at 850 °C (AC3-G) is still smaller than that at 760°C (AC1-AC3). That is because an “incubation period” must pass away before ferrite decarburization occurs in the temperature range of AC3-G, and the ferrite decarburized rate is limited to being equal to the partial decarburized rate.
Źródło:
Archives of Metallurgy and Materials; 2016, 61, 3; 1715-1722
1733-3490
Pojawia się w:
Archives of Metallurgy and Materials
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Using an Interdigital Micromixer for Separation of In3+ from Zinc Hydrometallurgical Process with D2EHPA as an Extractant
Autorzy:
Li, C.
Jiang, F.
Ju, S.
Peng, J.
Wei, Y.
Zhang, L.
Powiązania:
https://bibliotekanauki.pl/articles/356090.pdf
Data publikacji:
2017
Wydawca:
Polska Akademia Nauk. Czytelnia Czasopism PAN
Tematy:
interdigital micromixer
solvent extraction
mass transfer coefficient
indium
stripping
Opis:
Experiments were performed in an interdigital micromixer with 30 microchannels (40 μm width of each channel) to separate In3+, Fe3+ and Zn2+ from sulfate solutions using Di-(2-ethylhexyl)phosphoric acid (D2EHPA) as the extractant. The effects of pH, extractant concentration and flow rate on the extraction efficiency and flow rate on mass transfer coefficient of In3+, Fe3+ and Zn2+ were investigated. At a phase flow rate of 7.0 mL/min and initial solution pH of 0.423, the extraction efficiency of In3+, Fe3+ and Zn2+ was 99.29%, 3.43% and 2.54%, respectively and mass transfer coefficient of In3+, Fe3+ and Zn2+ was 144.307 s-1,1.018 s-1 and 0.750 s-1. Then, the loaded organic phase was stripped in an interdigital micromixer. At a phase flow rate of 9.0 mL/min and HCl concentration of 160 g/L, stripping efficiency of In3+ was 98.92% and mass transfer coefficient of In3+ was 169.808 s-1, while concentration of Fe3+ and Zn2+ was lower than 0.005 g/L with good separation of In3+ from Fe3+ and Zn2+.
Źródło:
Archives of Metallurgy and Materials; 2017, 62, 2A; 873-878
1733-3490
Pojawia się w:
Archives of Metallurgy and Materials
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Internal Friction of Li7La3Zr2O12 Based Lithium Ionic Conductors
Autorzy:
Wang, X. P.
Song, L.
Hu, J.
Xia, Y. P.
Xia, Y.
Gao, Y. X.
Zhang, L. C.
Magalas, L. B.
Fang, Q. F.
Powiązania:
https://bibliotekanauki.pl/articles/958222.pdf
Data publikacji:
2016
Wydawca:
Polska Akademia Nauk. Czytelnia Czasopism PAN
Tematy:
lithium ionic conductor
Li7La3Zr2O12
internal friction
Opis:
The diffusion mechanisms of lithium ions in tetragonal phase as well as in Al and Nb stabilized cubic Li7La3Zr2O12 compounds were investigated by low-frequency internal friction technique. In the cubic Li7La3Zr2O12 phase, a remarkable relaxation-type internal friction peak PC with a peak height up to 0.12 was observed in the temperature range from 15°C to 60°C. In the tetragonal phase however, the height of the PT peak dropped to 0.01. The obvious difference of the relaxation strength between the cubic and tetragonal phases is due to the different distribution of lithium ions in lattice, ordered in the tetragonal phase and disordered in the cubic phase. Based on the crystalline structure of the cubic garnet-type Li7La3Zr2O12 compound, it is suggested that the high internal friction peak in the cubic phase may be attributed to two diffusion processes of lithium ions: 96h↔96h and 96h↔24d.
Źródło:
Archives of Metallurgy and Materials; 2016, 61, 1; 21-24
1733-3490
Pojawia się w:
Archives of Metallurgy and Materials
Dostawca treści:
Biblioteka Nauki
Artykuł
    Wyświetlanie 1-3 z 3

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