Biogas and calcite handling in calcium fluoride precipitation from aqueous solution guided by thermodynamic simulation with PHREEQC.

In this innovative study, biogas has been associated with calcium carbonate [CaCO3] to promote the precipitation of fluorite, aiming at the treatment of wastewater with high content of fluoride. The work associates distinct sources of calcium and CO2 for the precipitation of fluorite according to previous simulation with the free software PHREEQC. Considering the reaction at equilibrium, the minimal predicted Ca dosage was 215 mg/L, lower than the 430 mg/L that was experimentally determined, independent of Ca source. The simultaneous use of CaCO3 and CO2 from distinct gas sources (pure CO2, 1:1 CO2:N2, and biogas) exhibited high performance permitting the reduction of fluoride content from 134 to 10 mg/L, with low gas consumption. The biogas consumption of 66.0 mmol/L, equivalent to 33.4 mmol/L of CO2 (1.47 kgCO2/m3treated wastewater) was predicted, indicating that the biogas storage bag of 700 L would be able to treat 469 L of wastewater. Furthermore, the inert fraction of biogas (CH4) did not impact the reaction and it may be used after the reaction as an alternative source of power, equivalent to 8.25 kWh/m3treated wastewater. Final solids were composed by fluorite and non-dissolved calcite, confirming the predictions obtained by PHREEQC.

Cow bones char as a green sorbent for fluorides removal from aqueous solutions: batch and fixed-bed studies.

Cow bone char was investigated as sorbent for the defluoridation of aqueous solutions. The cow bone char was characterized in terms of its morphology, chemical composition, and functional groups present on the bone char surface using different analytical techniques: SEM, EDS, N2-BET method, and FTIR. Batch equilibrium studies were performed for the bone chars prepared using different procedures. The highest sorption capacities for fluoride were obtained for the acid washed (q = 6.2 ± 0.5 mg/g) and Al-doped (q = 6.4 ± 0.3 mg/g) bone chars. Langmuir and Freundlich models fitted well the equilibrium sorption data. Fluoride removal rate in batch system is fast in the first 5 h, decreasing after this time until achieving equilibrium due to pore diffusion. The presence of carbonate and bicarbonate ions in the aqueous solution contributes to a decrease of the fluoride sorption capacity of the bone char by 79 and 31 %, respectively. Regeneration of the F-loaded bone char using 0.5 M NaOH solution leads to a sorption capacity for fluoride of 3.1 mg/g in the second loading cycle. Fluoride breakthrough curve obtained in a fixed-bed column presents an asymmetrical S-shaped form, with a slow approach of C/C 0 â†’ 1.0 due to pore diffusion phenomena. Considering the guideline value for drinking water of 1.5 mg F-/L, as recommended by World Health Organization, the service cycle for fluoride removal was of 71.0 h ([F-]feed âˆ¼ 9 mg/L; flow rate = 1 mL/min; m sorbent = 12.6 g). A mass transfer model considering the pore diffusion was able to satisfactorily describe the experimental data obtained in batch and continuous systems.