Flotation separation of wolframite from calcite using a new trisiloxane surfactant as collector

Since wolframite is usually associated with calcite,the separation and enrichment of wolframite by froth flotation remains a great challenge.Herein,a novel trisiloxane surfactant N-(2-aminoethyl)-3-ami nopropyltrisiloxane(AATS)was successful synthesized,which was used for the separation of wolframite from calcite for the first time.The flotation separation performance of AATS was studied by flotation test,and its adsorption mechanism was explored based on contact angle,infrared spectrum analysis(FTIR),zeta potential and density functional theory(DFT)calculation.The results of microflotation test and binary mixed ore flotation test pointed that AATS had excellent selectivity and more prominent collection capacity for the flotation of wolframite when compared with industrial reagent sodium oleate(NaOL).The measurement results of contact angle proved that AATS improved the hydrophobicity of the wolframite surface.The highly selective adsorption mechanism of AATS surfactant on mineral surfaces were further researched and analyzed by FTIR and zeta potential.The results revealed that AATS surfactant had significant adsorption effect on wolframite,yet almost no adsorption on calcite.DFT calculation indicated that AATS produced electrostatic adsorption with wolframite surface through—N+H3 group.

Recovery of vanadium and molybdenum from spent petrochemical catalyst by microwave-assisted leaching

The study of the leaching of vanadium(V) and molybdenum(Mo) from spent petrochemical catalysts in sodium hydroxide(NaO H) medium was performed using two approaches, namely, conventional leaching and microwave-assisted leaching methods. The influence of microwave power, leaching time, leaching temperature, and NaOH concentration on the leaching efficiency of spent petrochemical catalyst was investigated. Under microwave-assisted conditions(600 W, 10 min, 90°C, 2.0 mol·L^(-1) NaOH, and 0.20 g·mL^(-1) solid–liquid ratio), the leaching efficiencies of V and Mo reached 94.35% and 96.23%, respectively. It has been confirmed that microwave energy has considerable potential to enhance the efficiency of the leaching process and reduce the leaching time. It is suggested that the enhancement of the leaching efficiencies of V and Mo can be attributed to the existence of a thermal gradient between solid and liquid and the generation of cracks on the mineral surface.

Flotation performance and adsorption mechanism of novel 1-(2-hydroxyphenyl)hex-2-en-1-one oxime flotation collector to malachite

A novel collector 1-(2-hydroxyphenyl)hex-2-en-1-one oxime(HPHO)was synthesized from 2-hydroxy acetophenone and butyraldehyde.Its flotation performance and adsorption mechanism to malachite were investigated by flotation test,zeta potential,Fourier transform infrared(FTIR)and X-ray photoelectron spectroscopy(XPS)analysis techniques.Compared with benzohydroxamic acid(BA),1-(2-hydroxyphenyl)ethan-1-one oxime(HPEO)and sodium isobutyl xanthate(SIBX),HPHO exhibited excellent collecting power to malachite without additional reagents,such as Na2S regulator and methyl isobutyl carbinol(MIBC)frother.Results of zeta potential indicated that HPHO was coated on malachite surfaces through a chemisorption process.FTIR and XPS data gave clear evidence for the formation of Cu−oxime complex on malachite surfaces after HPHO adsorption through the linkage between C=C,—OH,N—OH group and Cu species.

Mechanism of sodium sulfide on flotation of cyanide-depressed pyrite

The mechanism of sodium sulfide(Na2S)on the flotation of cyanide-depressed pyrite using potassium amyl xanthate(PAX)as collector was investigated by flotation test and electrochemical measurements.The flotation results show that both PAX and Na2S can promote the flotation recovery of cyanide-depressed pyrite and their combination can further improve the pyrite flotation recovery.Electrochemical measurements show that PAX and Na2S interacted with cyanide-depressed pyrite through different mechanisms.PAX competed with cyanide and was adsorbed on the pyrite surface in the form of dixanthogen,thus enhancing the hydrophobicity and flotation of cyanide-depressed pyrite.Unlike PAX,Na2S rendered the pyrite surface hydrophobic through the reduction of ferricyanide species and the formation of elemental sulfur S0 and polysulfide Sn2-.The combined application of PAX and Na2S induced superior pyrite flotation recovery because of a synergistic effect between PAX and Na2S.

Flotation performance of a novel Gemini collector for kaolinite at low temperature

How to sustainably produce bauxite by effective reverse froth flotation of kaolinite at low temperature is an urgent problem to be solved in the field of mineral processing.In this work,a novel amino-based Gemini surfactant butadiyl-1,4-bis(dimethyl dodecylammonium bromide)(BBDB) was prepared and first utilized as a novel collector for kaolinite flotation.Its flotation performance for kaolinite was compared with that of the common monomolecular surfactant 1-dodecylamine(DDA) by micro-flotation tests.The tests results indicated that 95% kaolinite recovery was obtained using 2.0×10^(-4) mol/L BBDB at 25℃ which was half of the dosage when DDA obtained the maximum kaolinite recovery of81%.At extremely low temperature(0℃),3.0×10^(-4) mol/L BBDB could still collect 91% kaolinite,while DDA showed a frustrating ability.The contact angle tests indicated that BBDB could still significantly improve the hydrophobicity of the kaolinite surface(contact angle 71.7°) than DDA(contact angle only25.8°) at 0℃.The Krafft point comparison tests indicated that BBDB had a much lower Krafft point(below0℃) than DDA.Fourier transform infrared spectroscopy(FTIR)-spectrum analysis and zeta potential measurements showed that BBDB was physically adsorbed on the surface of kaolinite through electrostatic interaction.

Cu^2+-catalyzed mechanism in oxygen-pressure acid leaching of artificial sphalerite

The potential autoclave was used to study the catalytic mechanism of Cu^2+during the oxygen pressure leaching process of artificial sphalerite.By studying the potential change of the system at different temperatures and the SEM–EDS difference of the leaching residues,it was found that in the temperature range of 363–423 K,the internal Cu^2+formed a Cu S deposit on the surface of sphalerite,which hindered the leaching reaction,resulting in a zinc leaching rate of only 51.04%.When the temperature exceeds 463 K,the system potential increases steadily.The increase in temperature leads to the dissolution of the CuS,which is beneficial to the circulation catalysis of Cu^2+.At this time,the leaching rate of Zn exceeds 95%.In addition,the leaching kinetics equations at 363–423 and 423–483 K were established.The activation energy of zinc leaching at 363–423 and 423–483 K is 38.66 and 36.25 kJ/mol,respectively,and the leaching process is controlled by surface chemical reactions.

Effect of sintering temperature on microstructure and properties of glass-ceramics synthesized from waste cathode ray tubes funnel glass

Waste cathode ray tube(CRT)funnel glass(FG)is an important part in the disposal of electrical and electronic waste(e-waste).A novel approach for efficient lead extraction and glass-ceramics synthesized from waste FG through collaboratively smelting FG with coal fly ash(CFA)is proposed.Glass-ceramics materials with 40 wt%-80 wt%FG additions were produced under sintering temperatures of 900-1000℃.The microstructure and phase composition of the produced glass-ceramics were studied using X-ray diffraction(XRD)and scanning electron microscopy(SEM).The density,water absorption,Vicker hardness,chemical resistance and heavy metal leaching characteristics of the glassceramics were measured.The experimental results indicate that the samples can be crystallized at sintering temperatures of 900-1000℃.An elevated sintering temperature is favorable for enhancing the degree of crystallization,while the crystallization process is inhibited at excessively high temperatures.Increasing FG addition can lead to the transformation of the main crystalline phase from diopside to gehlenite.Well-crystallized crystals were generated in the specimens with 50 wt%-70 wt%FG additions.The samples with 40 wt%,50 wt%,60 wt%,70 wt%,80 wt%FG addition exhibit the optimal chemical and physical properties at 975,925,950,925 and 900℃,respectively.Overall results demonstrate that this study provides a feasible strategy for reliably detoxifying and reusing waste FG and CFA.