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.
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.
Hollow particles were prepared by the treatment of styrene-metbacrylic acid copolymer particles with alkali/cooling method. The influences of stirring position （in aqueous phase or at the interface of O/W） and stirring speed （90, 110 and 240 r/min） on the formation of hollow particles were investigated. It is found that the soft stirring in aqueous phase at 90 r/min leads to the formation of monohollow particles, while the violent stirring at the interface of O/W and 240 r/min gives non-hollow products. In contrast, the weak stirring in aqueous phase at 110 r/min results in sterically heterogeneous dispersion of methacrylic acid-rich regions within the original particles, and hence the formation of multihollow particles. Further investigation indicates that the change of stirring efficiency provides a way to tune the diffusion behavior of monomer styrene, and therefore influences the distribution of methacrylic acid units in the original particles as well as the morphology of the treated particles.
