Informacja

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

Wyszukujesz frazę "Zhao, Kaile" wg kryterium: Autor


Wyświetlanie 1-4 z 4
Tytuł:
Dispersion of sodium phytate on muscovite and the implications for arsenopyrite flotation
Autorzy:
Zou, Dan
Wang, Zhen
Zhao, Kaile
Xu, Ying
Powiązania:
https://bibliotekanauki.pl/articles/2175449.pdf
Data publikacji:
2022
Wydawca:
Politechnika Wrocławska. Oficyna Wydawnicza Politechniki Wrocławskiej
Tematy:
cassiterite
chlorite
sodium oleate
carboxymethyl cellulose
selective inhibition
Opis:
The effective flotation separation of sulfides and sliming silicate minerals is always a difficult problem. In this paper, the selective flotation of arsenopyrite from muscovite was studied by using sodium phytate (SP) as dispersant, and the mechanism was investigated through SEM/EDS, zeta potential, FTIR and XPS measurements. Single mineral flotation results showed that with the increasing isoamyl xanthate (IAX) dosage the recovery of arsenopyrite increased, until 8×10−5 mol/L IAX (79.40% recovery, pH=7), after that it decreased slightly. While muscovite floated poorly at any IAX concentration. For the mixed minerals, arsenopyrite recovery was only 54.63% while that of muscovite was 42.70%, which was attributed to the coverage of muscovite on arsenopyrite surface. When 6×10−5 mol/L SP was added into the mixed minerals system, the recovery of arsenopyrite recovered to 68.26% while that of muscovite was 8.48% (approximate the value of the single mineral). SEM/EDS results showed that SP could disperse muscovite and prevented its coverage on arsenopyrite surface. Zeta potential results showed that the electrokinetic potential of muscovite and arsenopyrite decrease from -26.60mV to -39.01 mV and from -26.90 mV to -27.84 mV at pH=7, respectively. It was obvious that the negatively charged phytate ions selectively adsorbed on the surface of muscovite. FTIR and XPS resulted co-proved the chemisorption of SP with active sites on muscovite while arsenopyrite spectrum did not change significantly, which was consistent with flotation and zeta potential results. The selective adsorption of SP on muscovite compared to arsenopyrite was responsible for the effective separation of them.
Źródło:
Physicochemical Problems of Mineral Processing; 2022, 58, 6; art. no. 154951
1643-1049
2084-4735
Pojawia się w:
Physicochemical Problems of Mineral Processing
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Adsorption of yeast dextran on clinochlore surface and the implications for pyrite/clinochlore separation
Autorzy:
Wang, Zhen
Zou, Dan
Zhao, Kaile
Safarov, Sayfidin
Xu, Ying
Powiązania:
https://bibliotekanauki.pl/articles/2146917.pdf
Data publikacji:
2022
Wydawca:
Politechnika Wrocławska. Oficyna Wydawnicza Politechniki Wrocławskiej
Tematy:
clinochlore
pyrite
flotation
yeast dextran
adsorption
Opis:
Silicate minerals with a certain degree of flotability are often easy to mix into sulfide ore concentrate in mineral processing industry. In this paper, the adsorption of yeast dextran on clinochlore and its application in pyrite/clinochlore separation were investigated. The adsorbed amount and micro polarity measurement results displayed that the yeast dextran molecules selectively adsorbed onto clinochlore surface compared with pyrite. The adsorbed yeast dextran resulted in the increase in the surface polarity of clinochlore surface, and inhibited the further adsorption of xanthate, thus keep it hydrophilic and depressed. Quantum chemical computation results indicated that yeast dextran was mainly adsorbed on mineral surface by the chelation with the surface metal active sites, and the chelating strength of yeast dextran with three ions was in the sequence of Fe3+ > Mg2+ > Fe2+. While Mg2+, Fe2+ and Fe3+ are the main metal ions on the surface of clinochlore, and Fe2+ is the unique metal ions on pyrite surface. This is the reason of the selectivity of the yeast dextran depressant for pyrite/clinochlore flotation system. The flotation results demonstrated that yeast dextran was qualified to selectively depress clinochlore in pyrite flotation.
Źródło:
Physicochemical Problems of Mineral Processing; 2022, 58, 4; art. no. 151635
1643-1049
2084-4735
Pojawia się w:
Physicochemical Problems of Mineral Processing
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
The effect of a novel depressant on the separation of talc and copper –nickel sulfide ore
Autorzy:
Gu, Guohua
Chen, Zhixiang
Zhao, Kaile
Song, Siyu
Li, Shuangke
Wang, Chongqing
Powiązania:
https://bibliotekanauki.pl/articles/110492.pdf
Data publikacji:
2019
Wydawca:
Politechnika Wrocławska. Oficyna Wydawnicza Politechniki Wrocławskiej
Tematy:
Sodium alginate
talc
copper–nickel sulfide
polysaccharide depressant
flotation
Opis:
This paper researched the influence of the polysaccharide polymer sodium alginate (SAG) on the depression of talc at a fixed room temperature about 25 °C through micro flotation and batch flotation experiments, zeta potential and contact angle measurements as well as infrared spectroscopy analysis. The flotation results displayed that the SAG had a significant influence on the flotation of talc but less influence on sulphide flotation. Compared with the depressant carboxymethyl cellulose (CMC) and guar gum, using of the SAG gave the highest copper recovery. It could not only eliminate a talc removal step, but also significantly decrease in the depressant consumption by half at least. Sodium alginate apparently adsorbs on the talc surface and promotes hydrophilization, as revealed by contact angle tests (contact angle decreased from 75 to 33° after treating with SAG). It is demonstrated that the SAG obviously absorbed at the surface of talc but rarely for chalcopyrite through the results of zeta potential measurements and infrared spectroscopy analysis.
Źródło:
Physicochemical Problems of Mineral Processing; 2019, 55, 1; 116-127
1643-1049
2084-4735
Pojawia się w:
Physicochemical Problems of Mineral Processing
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Improved flotation of auriferous arsenopyrite by using a novel mixed collector in weakly alkaline pulp
Autorzy:
Wang, Xiaohui
Zhao, Kaile
Bo, Hui
Yan, Wu
Wang, Zhen
Gu, Guohua
Gao, Zhiyong
Powiązania:
https://bibliotekanauki.pl/articles/1845220.pdf
Data publikacji:
2020
Wydawca:
Politechnika Wrocławska. Oficyna Wydawnicza Politechniki Wrocławskiej
Tematy:
gold mine
arsenopyrite
mixed collector
flotation
Opis:
The purpose of using a mixed collector is to increase both flotation efficiency and selectivity. The mixed collector of potassium isopentyldithiocarbonate and N-dodecyl mercaptan exhibits high efficiency for the flotation of auriferous arsenopyrite, and the 2:1 mixing mass ratio of potassium isopentyldithiocarbonate and N-dodecyl mercaptan is preferred. Batch flotation tests indicate that a concentrate with the grade of 47.58 g/Mg Au and the recovery of 86.45% Au is achieved by using the mixed potassium isopentyldithiocarbonate/N-dodecyl mercaptan in weakly alkaline pulp. The collector mixture potassium isopentyldithiocarbonate + N-dodecyl mercaptan has greater adsorption density on the arsenopyrite surface than other conventional mixed collectors. The mixed potassium isopentyldithiocarbonate/N-dodecyl mercaptan can adsorb onto the arsenopyrite surface by intense chemisorptions, and the Sulfur-Iron chemical complexation is considered as the main adsorption mode. This is the reason why mixed potassium isopentyldithiocarbonate and N-dodecyl mercaptan collector can improve the flotation efficiency of auriferous sulfides.
Źródło:
Physicochemical Problems of Mineral Processing; 2020, 56, 5; 996-1004
1643-1049
2084-4735
Pojawia się w:
Physicochemical Problems of Mineral Processing
Dostawca treści:
Biblioteka Nauki
Artykuł
    Wyświetlanie 1-4 z 4

    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