PL EN


Preferencje help
Widoczny [Schowaj] Abstrakt
Liczba wyników
Tytuł artykułu

Behavior and mechanism of collophane and dolomite separation using alkyl hydroxamic acid as a flotation collector

Autorzy
Treść / Zawartość
Identyfikatory
Warianty tytułu
Języki publikacji
EN
Abstrakty
EN
Flotation response of collophane and dolomite using alkyl hydroxamic acid (AH) (chelating collector) was investigated in the paper. The experiments were performed using pure and artificially mixed minerals as well as a real phosphate ore. Their separation mechanisms were studied by means of zeta potential measurements, infrared analysis, adsorption measurements, thermodynamics, and quantum chemical calculations. The results indicated that AH exhibited an excellent performance in the flotation separation of collophane from dolomite in neutral medium. The P2O5 grade of the concentrate increased from 19.84% to 30.51% without any other reagents when the pH value was about 7. The zeta potential and adsorption studies showed that the adsorption of AH at the cellophane/aqueous interface was greater than that at dolomite surface, which was the essential reason that separation of collophane from dolomite. The results of Fourier Transform Infrared (FTIR) spectrum and thermodynamics calculation indicated that the adsorption of AH at collophane was attributed to the chemical bonding. Moreover, AH molecule formed O-O five-membered ring with calcium ion on the collophane surface.
Słowa kluczowe
Rocznik
Strony
155--169
Opis fizyczny
Bibliogr. 20 poz., rys., tab.
Twórcy
autor
  • School of Resources and Environmental Engineering, Wuhan University of Technology, Wuhan 430070, PR China
autor
  • School of Resources and Environmental Engineering, Wuhan University of Technology, Wuhan 430070, PR China
autor
  • School of Resources and Environmental Engineering, Wuhan University of Technology, Wuhan 430070, PR China
Bibliografia
  • ABOUZEID A.Z.M., NEGM A.T., ELGILLANI D.A., 2009, Upgrading of calcareous phosphate ores by flotation: Effect of ore characteristics, International Journal of Mineral Processing, 90, 81–89.
  • AHMED H.A.M., ALJUHANI M.S., DRZYMALA J., 2013, Flotation after direct contact of flotation reagents with particles. Part I. Model investigations, Physicochemical Problem of Mineral Processing, 49(2), 713–723.
  • AL-FARISS T.F.,ARAFAT Y., ABD EL-ALEEM F.A.E., L-MIDANY A.A., 2014, Investigating sodium sulphate as a phosphate depressant in acidic media, Separation and Purification Technology, 124, 163–169.
  • BOULOS T.R., YEHIA A.,IBRAHIM, S.S. and YASSIN, K.E., 2014, A modification in the flotation process of a calcareous–siliceous phosphorite that might improve the process economics, Minerals Engineering, 69, 97–101.
  • DOS SANTOS M.A., SANTANA R.C., CAPPONI F., ATAIDE C.H., BARROZO M.A.S., 2012, Influence of the water composition on the selectivity of apatite flotation, Separation Science and Technology, 47(4), 606-612.
  • ELMAHDY A.M., EL-MOFTY S.E., ABDEL-KHALEK M.A., ABDEL-KHALEK N.A., EL-MIDANY A.A., 2013, Bacterially induced phosphate–dolomite separation using amphoteric collector, Separation and Purification Technology, 102, 94–102.
  • GE Y.Y., HUANG L., XIONG X.H., YU Y.F., 2014, Mechanism of a new collector alkyl polyamine ether adsorption onjasper and magnetite, Journal of Central South University, 45(5), 1377–1382.
  • JIANG Y., ZHAO B., ZHOU X.H., ZHOU L.Y., 2010, Flotation of diaspore and aluminosilicate minerals applying novel carboxyl hydroxamic acids as collector, Hydrometallurgy, 104(1), 112–118.
  • LIU A., FAN J.C., FAN M.Q., 2014, Quantum chemical calculations and molecular dynamics simulations of amine collector adsorption on quartz (001) surface in the aqueous solution, International Journal of Mineral Processing, 134, 1–10.
  • MERMA A.G., TOREM M.L., MORAN J.J.V., MONTE M.B.M., 2013, On the fundamental aspects of apatite and quartz flotation using a Gram positive strain as a bioreagent, Minerals Engineering, 48, 61–67.
  • MOHAMMADKHANI M., NOAPARAST M., SHAFAEI S.Z., AMINI A., AMINI E., ABDOLLAHI H., 2011, Double reverse flotation of a very low grade sedimentary phosphate rock, rich in carbonate and silicate, International Journal of Mineral Processing, 100(3-4), 157–165.
  • NANTHAKUMAR B., GRIMM D., PAWLIK M., 2009, Anionic flotation of high-iron phosphate ores – Control of process water chemistry and depression of iron minerals by starch and guar gum, International Journal of Mineral Processing, 92(1-2), 49–57.
  • SANTANA R.C., DUARTE C.R., ATAIDE C.H., BARROZO M.A.S., 2011, Flotation selectivity of phosphate ore: Effects of particle size and reagent concentration, Separation Science and Technology, 46(9), 1511–1518.
  • SANTANA R.C., RIBEIRO J.A., SANTOS M.A., REIS A.S., ATAIDE C.H., BARROZO M.A.S., 2012, Flotation of fine apatitic ore using microbubbles, Separation and Purification Technology, 98, 402–409.
  • SANTANA R., FARNESE A., FORTES M., ATAIDE C., BARROZO M., 2008, Influence of particle size and reagent dosage on the performance of apatite flotation, Separation and Purification Technology, 64(1), 8–15.
  • SIS H., CHANDER S., 2003, Reagents used in the flotation of phosphate ores: a critical review, Minerals Engineering, 16(7), 577–585.
  • WANG P., QIN W., REN L.Y., WEI Q., 2013, Solution chemistry and utilization of alkyl hydroxamic acid in flotation of fine cassiterite, Transactions of Nonferrous Metals Society of China, 23 (6), 1789–1796.
  • WANG X., NGUYEN A.V., MILLER J.D., 2006, Selective attachment and spreading of hydroxamic acid–alcohol collector mixtures in phosphate flotation, International Journal of Mineral Processing, 78 (2), 122–130.
  • ZHAO G., ZHONG H., QIU X.Y., WANG S., GAO Y.D., 2013, The DFT study of cyclohexylhydroxamic acid as a collector in scheelite flotation, Minerals Engineering, 49, 54–60.
  • ZHU D., ZHU Y.S., 1993, Dynamic study on adsorption of octylhydroximic acid on the surfaces of cassiterite, Mining and Metallurgical Engineering, 13(4), 41–43.
Typ dokumentu
Bibliografia
Identyfikator YADDA
bwmeta1.element.baztech-bf2b5973-1d53-4bb8-8e69-fb60fb0f94cb
JavaScript jest wyłączony w Twojej przeglądarce internetowej. Włącz go, a następnie odśwież stronę, aby móc w pełni z niej korzystać.