RESUMO
The extraction and recovery of valuable metals from various spent catalysts via bioleaching represents a green, low-carbon and eco-friendly process. However, the pulp density of spent catalysts is usually 1.0% or lower owing to their toxicity, denoting low process capacity and poor practical potential. In this study, an intensified bioleaching strategy was used for the first time to promote the release efficiencies of both Co and Mo from a spent Co-Mo catalyst at a high pulp density of 10% by supplementing extracellular polymeric substances (EPSs). The results showed that the addition of 0.6 g L-1 EPSs harvested a maximum release of 73.6% for Co and 72.5% for Mo after 9 days of contact, with an evident elevation of 22.6% for Co and 24.4% for Mo, in contrast to no addition, respectively. The added EPS not only promoted the growth of plankton cells to produce more active molecules but also boosted the adhesion of leaching cells to the spent catalyst to form stable aggregates. Moreover, the resulting aggregates allowed for the gathering and confinement of the active small molecules, including Fe3+ and Fe2+, inside the micro-areas between the spent catalysts and the cells for quick electronic transfer as an interface oxidation/reduction reaction to free both Co and Mo from the spent catalyst.
RESUMO
Waste copper-containing paint residue (WCPR) represents a typical hazardous waste containing both toxic organic substances and toxic heavy metals, but there are few reports on the recycling of heavy metals. The recovery of Cu from WCPR by H2SO4 leaching-extraction-stripping has the advantages of eco-friendliness, simplicity of operation, and high value-added product. The results show that under the optimal conditions, the leaching rate of Cu in WCPR is 94.31% (18.02 g/L), while the extraction and stripping rates of Cu in the leaching solution are 99.46 and 95.32%, respectively. Due to the high concentration of Cu2+ with fewer impurities in the stripping solution, the stripping solution is heated, evaporated, cooled, and crystallized to successfully produce high-purity dark blue CuSO4 crystal, accomplishing the high-value recycling of Cu in WCPR. In addition, the leach residue of WCPR contains acrylic resin and SiO2, which can be used in cement kilns for incineration, thus realizing the overall recycling and utilization of WCPR.
Assuntos
Cobre , Metais Pesados , Dióxido de Silício , Metais Pesados/química , Reciclagem , PinturaRESUMO
Waste zinc-rich paint residue (WZPR) represents a typical hazardous waste containing both toxic organic substances and heavy metals. The extraction of Zn from WZPR by traditional direct bioleaching has been attracting attention owing to its eco-friendliness, energy conservation and low cost. However, a long bioleaching time and a low Zn release cast a shadow on the reputed bioleaching. To shorten the bioleaching time, the spent medium (SM) process was first used to free Zn from WZPR in this study. The results showed that the SM process had a much higher performance in Zn extraction. Zn removals of 100% and 44.2% (8.6 g/L and 15.2 g/L in the released concentration) were gained within 24 h under pulp densities of 2.0% and 8.0%, respectively, being over 1000 times of the release performance of Zn by previously reported direct bioleaching. On the one hand, the biogenic H+ in SM attacks ZnO to liberate Zn (â ¡) via quick acid dissolution. On the other hand, the biogenic Fe3+ not only highly oxidizes Zn0 in WZPR to generate and release Zn2+ but also intensely hydrolyzes to produce H+ to attack ZnO for further dissolution of Zn2+. Both biogenic H+ and Fe3+ contribute to over 90% of Zn extraction as the leading indirect bioleaching mechanism. Due to the high concentration of released Zn2+ and fewer impurity, the bioleachate was used to successfully produce high-purity ZnCO3/ZnO using a simple precipitation, thus achieving the high-value recycling of Zn in WZPR.