Chlorite and serpentine are common magnesium-containing gangue minerals in copper sulfide flotation. In this study, sodium alginate, a natural hydrophilic polysaccharide, was introduced as a selective depressant for these gangue minerals. Micro-flotation tests were conducted on both single minerals and synthetic mixtures. The flotation results showed that sodium alginate could simultaneously depress the flotation of chlorite and serpentine effectively, but seldom influenced the floatability of chalcopyrite at pH 9. In the ternary mixture flotation, a concentrate with a Cu grade of 31% could be achieved at Cu recovery of 90%. The selective depression of chlorite and serpentine was also validated by the real ore flotation experiments. The selective depression mechanism was investigated through adsorption tests, zeta potential measurements, and FTIR analyses. The adsorption density results implied that sodium alginate selectively adsorbed on the surface of phyllosilicates, but no adsorption on the chalcopyrite surface was observed. The zeta potential results showed that the sodium alginate could selectively decrease the surface charge of chlorite and serpentine. The FTIR results revealed the chemical adsorption of sodium alginate on the chlorite and serpentine surface and no form of adsorption on chalcopyrite, agreeing well with the adsorption density results. On the basis of these results, a selective adsorption model of sodium alginate on the mineral surface was proposed.

Development of active and earth-abundant catalysts is pivotal to render hydrazine monohydrate (N₂H₄·H₂O) viable as a hydrogen carrier. Herein, we report the synthesis of noble-metal-free Ni–W–O-derived catalysts using a hydrothermal method in combination with reductive annealing treatment. Interestingly, the thus-prepared Ni-based catalysts exhibit remarkably distinct catalytic properties toward N₂H₄·H₂O decomposition depending upon the annealing temperature. From a systematic phase/microstructure/chemical state characterization and the first-principles calculations, we found that the variation of the apparent catalytic properties of these Ni-based catalysts should stem from the formation of different Ni–W alloys with distinct intrinsic activity, selectivity, and distribution state. The thereby chosen Ni–W alloy nanocomposite catalyst prepared under an optimized condition showed high activity, nearly 100% selectivity, and excellent stability toward N₂H₄·H₂O decomposition for hydrogen production. Furthermore, this noble-metal-free catalyst enables rapid hydrogen production from commercially available N₂H₄·H₂O solution with an intriguingly high hydrogen capacity of 6.28 wt % and a satisfactory dynamic response property. These results are inspiring and momentous for promoting the use of the N₂H₄·H₂O-based H₂ source systems.

In industrial practice, hydrodynamic cavitation (HC) is commonly triggered by jetting either reagent solution or pulp. Although both methods can enhance mineral flotation, are their roles the same? There are few research studies in the field, which severely limits our understanding on mineral flotation combined with HC. Therefore, in this study, the flotation of ultrafine scheelite with HC pretreatments of reagent solution and pulp (abbreviated to be HCPS and HCPP, respectively) was studied and compared through flotation tests, zeta potential analysis, microscope tests, and shear yield stress measurements. The results of flotation tests show that both HCPS and HCPP can enhance the final flotation performance, but in general, HCPP leads to greater improvements on the final flotation recovery. The presence of (hydrophobized) scheelite particles brings extra gas nuclei for the cavitation–flotation system, suggesting that more NBs may be produced in the case of HCPP compared with HCPS. These tiny bubbles remarkably reduce the size distribution of bubbles in the flotation system, thus increasing the particle–bubbles collision probability. Increase in particle aggregation may be another reason why flotation with HCPP results in a higher flotation recovery. The adherence of NBs on hydrophobized particles decreases the (absolute) surface charge of the solids, resulting in a smaller repulsive force among particles and more significant particle aggregation, which is confirmed by the microscope tests and shear yield stress measurements.

The influence of conditioning on the flotation of pyrrhotite in the presence of chlorite was investigated through flotation tests, sedimentation tests, and X-ray photoelectron spectroscopy (XPS) analysis. The flotation results show that chlorite slimes dramatically impair the flotation of pyrrhotite. Sedimentation and flotation tests reveal that conditioning can effectively remove chlorite slimes from pyrrhotite surfaces, resulting in an enhanced flotation recovery of pyrrhotite. When mixed minerals were conditioned under the natural atmosphere, a faster conditioning speed and longer conditioning time decreased the flotation recovery of pyrrhotite. However, when mixed minerals were conditioned under a nitrogen atmosphere, a more intensive conditioning process provided better flotation results. XPS analyses illustrate that a faster conditioning speed and longer conditioning time under the natural atmosphere accelerates the oxidation of pyrrhotite, leading to a decrease in the flotation recovery of pyrrhotite.