Abstract
Phosphoric acid production generates large volumes of industrial wastewater that cannot be treated efficiently by existing processes because of its low pH and high precipitation potential. At present, the wastewater is generally stored in evaporation ponds that are prone to breaches, leakage, and flooding. We developed an alternative three-step process for the treatment of phosphoric acid wastewater including selective electrodialysis, reverse osmosis, and neutralization. Testing the process with synthetic wastewater yielded promising results. An exceptional Na/Ca selectivity (up to 18.3 was observed in low-pH electrodialysis, enabling the separation of concentrated H2SO4 without gypsum scaling. Sulfate removal from the electrodialysis diluate prevented scaling in the subsequent high-recovery (>90%) reverse osmosis step, generating high-quality water. A final reaction between the reverse osmosis concentrate and natural phosphate rock enabled P recovery and neutralization of remaining acidity. The electric-power requirement of the process was estimated to be 4.4 kWh per m3 of wastewater, from which 0.78 m3 of clean water, ~3 kg H2SO4, and ~2.5 kg P were recovered. Overall, lab-scale results indicate that this process would be a sustainable and techno-economically viable solution for the treatment of hazardous wastewater byproducts of the phosphoric acid industry
Supplementary materials
Title
Supporting Information
Description
Properties of the commercial membranes in the ED stack, details of current efficiency and selectivity calculations, the evolution of ED process parameters in the high-recovery experiments including ion transport, pH, EC, and current density variation with time in the diluate compartment, and SEC values are described in the Supporting Information.
Properties of the cross-flow filtration system and feed composition for the RO system, including PHREEQC simulations and related calculations to correct for concentration polarization, SEM imaging, SEM–EDS, and XRD results are also described in the Supporting Information.
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