Four modified starches with selected charge characteristics including cationic starch(CAS),carboxymethyl starch(CMS),amphoteric starch(AMS) and soluble starch(SS) were investigated as depressants for diaspore in reverse flotation test using cationic collector(dodecylamine).Adsorption examination,Zeta potential measurement and Fourier transform infrared(FTIR) spectroscopy were used to clarify the role of the surface charge characteristics of starches in determining the adsorption behavior and depression performance as well as the mineral-starch interaction.Results show that the positively charged starches(CAS and AMS) display higher adsorption amounts and also better depression performance compared with the non-ionic(SS) and anionic starch(CMS),benefiting from the favorable electrostatic attraction with diaspore and also electrostatic repulsion with collector.FTIR spectroscopy proves the presence of hydrogen bonds and chemical complexation between mineral and starches in an integrated manner.
The adsorption of dedecyltrimethylammoium chloride(DTAC) and hexadecyltrimethylammoium chloride(CTAC) on muscovite mica substrates was examined using atomic force microscopy(AFM). Adsorption morphology images and interaction forces of cationic surfactants at solid-solution interfaces were measured in tapping mode and Pico Force mode, respectively. The images demonstrated that the adsorbed structure was varied by a variety of surfactant concentrations. The adsorbed layer on mica was monolayer at first, and then became bilayer. A striped adsorbed structure was observed in a higher concentration of CTAC,which could not be found in any other concentrations of DTAC. For force measurements, the repulsive force was exponentially decreasing with the concentration increasing till a net attractive force appeared. A largest attractive force could be observed at a certain concentration, which was close to the point of charge neutralization. The results also showed a significant impact of hydrocarbon chain length on adsorption. An adsorption simulation was established to give a clear understanding of the interaction between cationic surfactants and mica.
Carboxymethyl starchs（CMS） with low and high degrees of substitution（CMSL and CMSH in short,respectively） were employed as depressants of diaspore in cationic reverse flotation using dodecylamine（DDA） as collector.The effect of degree of substitution of CMS on its depression performance was examined and the interaction mode and behavior were investigated in a comparative manner.Micro-flotation test showed that CMSL exhibited better performance in depressing diaspore than CMSH in a broad pH range.The adsorption of CMS on diaspore was studied by adsorption test,zeta potential measurement,and atomic force microscopy.It was found that CMSH corresponds to lower adsorption amount,thinner adsorption layer,and more negative charge than CMSL,resulting from the more chelating sites brought by the high degree of substitution.The surface tension measurement and DDA adsorption test further revealed that CMSL/DDA system gives a better depressing performance benefiting from the trapping effect by enveloping some DDA molecules inside the loop chains,while CMSH/DDA system is likely considered a quasi-surfactant.
The flotation behaviors of decyltrimethylammonium (103C), dodecyltrimethylammonium chloride (DTAC), tetradecyltrimethylammonium chloride (TTAC) and cetyltrimethylammonium chloride (CTAC) on kaolinite of different particle size fraction were studied. The adsorbed amount and adsorption isotherms of collectors on kaolinite were determined for painstaking investigation into the adsorption of quaternary amines at kaolinite-water interface by ultraviolet spectrophotometer methods. The flotation results show that the flotation recovery of kaolinite of different particle fraction increases with an increase in pH when 103C, DTAC, TTAC and CTAC are used as collectors. As the concentration of collectors increases, the flotation recovery increases. Particle size of kaolinite has a strong effect on flotation. The flotation recovery of fine kaolinite decreases with the carbon chain of quaternary ammonium salts collectors increasing, while coarse kaolinite is on the contrary. The adsorbed amount tests and adsorption isotherms show that adsorbed amount increases when the particle size of kaolinite increases or when the carbon chain length of quaternary ammonium salts increases. Within the range of flotation collector concentration, the longer the hydrocarbon chain, the more probable to be absolutely adsorbed by fine kaolinite particles and then the lower the collector concentration in the bulk, which leds to lower flotation recovery.
The flotation and adsorption behaviors of dodecyltrimethylammonium chloride（DTAC） and cetyltrimethylammonium chloride（CTAC） on diaspore and kaolinite were studied.Solution depletion methods were used to determine adsorption isotherms.Fluorescence probe test along with Zeta potential measurement was also conducted for further investigation into the adsorption of quaternary amines at the mineral-water interface.The results show that the flotation recovery of kaolinite decreases with an increase in pH when DTAC and CTAC are used as collectors,while diaspore is on the contrary.As the carbon chain length of the collectors increases,the flotation recoveries of minerals increase.However,the increment rate of kaolinite is significantly lower than that of diaspore.In the low surfactant concentration range,the cationic surfactants adsorb readily on diaspore surfaces just due to electrostatic interactions.As for kaolinite surfaces,ion exchange process also exists.With a further increase in surfactant concentration,the adsorption was ascribed to the hydrophobic association of chain-chain interactions.Micro-polarity of mineral surfaces study shows that CTAC has a better hydrophobic characteristic than DTAC.Larger aggregates are formed with CTAC on diaspore than on kaolinite in the same solution concentration.The results also indicate that the chain length of cationic surfactants has a greater influence on the adsorption of diaspore than on kaolinite,which is consistent with the flotation result.
