Informacja

Drogi użytkowniku, aplikacja do prawidłowego działania wymaga obsługi JavaScript. Proszę włącz obsługę JavaScript w Twojej przeglądarce.

Wyszukujesz frazę "Cao, Yang" wg kryterium: Autor


Wyświetlanie 1-2 z 2
Tytuł:
A first-principle study of the effect of Fe/Al impurity defects on the surface wettability of dolomite
Autorzy:
Chen, Hong
Ao, Xianquan
Cao, Yang
Li, Cuiqin
Jiang, Chunyan
Powiązania:
https://bibliotekanauki.pl/articles/2146916.pdf
Data publikacji:
2022
Wydawca:
Politechnika Wrocławska. Oficyna Wydawnicza Politechniki Wrocławskiej
Tematy:
density functional theory
phosphate rock flotation
dolomite
surface wettability
density of states
Opis:
The presence of Fe and Al atoms in large quantities in phosphate ores can significantly affect the surface properties of the minerals during flotation. In this study, the effects of Fe/Al impurities on the adsorption of H2O molecules on dolomite, including the density of states (DOS), Mulliken bond group values, and charge groups, were investigated and the adsorption energy was analyzed using density functional theory. The results show that the adsorption of H2O molecules on perfect and Fe/Al-substituted dolomites is weak chemisorption, and the Fe and Al impurities weaken and enhance the adsorption capacity of H2O molecules, respectively. Therefore, the hydrophilicity of the dolomite surface increases in the following order: Fe-substituted dolomite < perfect dolomite < Al-substituted dolomite. The Mulliken charge and bond group analysis shows that the adsorption of H2O molecules on dolomite is primarily through the interaction between Ow and Ca atoms, where the d orbitals of Ca atoms provide charges for Ow atoms to form ionic bonds, which related to the poor electronegativity of Ca atoms and their weak valence electron binding ability. The DOS analysis shows that, during the adsorption of H2O molecules on dolomite, Mg and Al atoms have less influence on the dolomite surface, whereas Fe and Ca atoms undergo competitive adsorption, which inhibits the interaction between Ca atoms and H2O molecules on the dolomite surface.
Źródło:
Physicochemical Problems of Mineral Processing; 2022, 58, 4; art. no. 150702
1643-1049
2084-4735
Pojawia się w:
Physicochemical Problems of Mineral Processing
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Separation and purification of light rare earth elements from chloride media using P204 and Cyanex272 in sulfonated kerosene under non-saponification conditions
Autorzy:
Fan, Peiqiang
Zhang, Wenjie
Tong, Xiong
Xie, Xian
Xie, Ruiqi
Song, Qiang
Du, Yunpeng
Cao, Yang
Powiązania:
https://bibliotekanauki.pl/articles/27323661.pdf
Data publikacji:
2023
Wydawca:
Politechnika Wrocławska. Oficyna Wydawnicza Politechniki Wrocławskiej
Tematy:
P 204
Cyanex 272
light rare earths
extraction
mechanism
Opis:
The extraction of light rare earths (Pr and Nd) from chloride medium was investigated using a mixture of di(2-ethylhexyl) phosphoric acid (P204) and bis(2,4,4-trimethylpentyl) phosphinic acid (Cyanex272) in sulfonated kerosene. The P204+Cyanex272 system exerted a synergistic effect on the separation of light rare earths, and the separation coefficient was higher than when P204 and Cyanex272 were used as extractants alone. The separation coefficient of Pr and Nd in the extraction system reached 1.75 when the pH of the aqueous phase material solution was approximately 2.5, and 1.5 mol/L hydrochloric acid as a stripping agent effectively eluted the rare earth ions in the loaded organic phase. Combining the slope method, infrared spectroscopy, and nuclear magnetic resonance spectroscopy, we explored the mechanism of the extracted Nd and Pr into the organic phase complex, and finally entered the organic phase with Re(HA2)2B. The P-O-H bond and P=O bond in the extractant P204 and Cyanex272 formed a coordination bond with Re3+. Therefore, this extraction method also provides a reference for a more environmentally friendly and efficient procedure for separation and purification of light rare earth elements Pr and Nd.
Źródło:
Physicochemical Problems of Mineral Processing; 2023, 59, 6; art. no. 172444
1643-1049
2084-4735
Pojawia się w:
Physicochemical Problems of Mineral Processing
Dostawca treści:
Biblioteka Nauki
Artykuł
    Wyświetlanie 1-2 z 2

    Ta witryna wykorzystuje pliki cookies do przechowywania informacji na Twoim komputerze. Pliki cookies stosujemy w celu świadczenia usług na najwyższym poziomie, w tym w sposób dostosowany do indywidualnych potrzeb. Korzystanie z witryny bez zmiany ustawień dotyczących cookies oznacza, że będą one zamieszczane w Twoim komputerze. W każdym momencie możesz dokonać zmiany ustawień dotyczących cookies