Soil contamination by heavy metals through the application of a phosphate fertilizer is a key issue for sustainable agriculture. Among contaminants, cadmium (Cd) is considered the most hazardous to human beings’ health and the surrounding environment. X-ray diffraction (XRD), combined with binocular mineralogical analysis and chemical analysis, was used to determine the C(I) and C(II) layers’ composition. In the C(II) (+71 µm)-size fraction, the presence of carbonate-fluorapatite, illite, and montmorillonite was revealed, whereas in the C(I) (−71 µm)-size fraction, carbonate-fluorapatite, calcite, quartz, sanidine, clinoptilolite, and taramovite were identified. The P₂O₅ and CaO contents were greater in the C(II) layer than that in the C(I) layer, whereas SiO_2, MgO, CO₂, Cd, Zn, and CO_rg were higher in the C(I) layer than that in the C(II) layer. The bioleaching of Cd from phosphate rock samples from the Kef Eddour deposit was investigated using three bacterial strains isolated from the local phosphate environment. A decrease in cell viability was noticed when the phosphate C(I) and C(II) samples showed toxicity in the samples. In addition, the isolated bacteria, which were initially moderately hydrophobic, changed to strongly hydrophobic. The use of the consortium (S1 + S2 + S3) was the most powerful combination to reduce the Cd content, which increased from 13.31% to 29.07% using S3 and the consortium (S1 + S2 + S3), respectively, when the C(II) (+71 µm)-size fraction sample was added to the medium. The same result was shown when the C(I) (−71 µm)-size fraction sample was used. The isolated strains could be used as a biological tool for bioleaching.

The present study describes the influence of potassium and hydroxyl substitutions on the structural, thermal and mechanical properties of fluorapatite bioceramics. A set of non-stoichiometric ion-substituted compounds, with a chemical formula of Ca_10−xK_x(PO₄)₆F_(2−2x)(OH)_x with 0 ≤ x ≤ 1 synthesized by the wet precipitation method, were found to be single-phase apatites crystallizing in the hexagonal P6₃/m space group. The structural parameters, as well as the crystallite sizes, increased accordingly to the amount of added dopant-ions. The thermal behavior of these compounds, studied within the temperature range 500–1200 °C, indicated a partial decomposition of the apatitic phase and its transformation to tricalcium phosphate β-Ca₃(PO₄)₂ at temperatures exceeding 750 °C. A relative density of the sintered samples achieved the highest value with x = 0.25 and reached about 95% after sintering at 1050 °C for 1 h. The microstructures of the sintered samples were of a trans-granular aspect and experienced an increase in the radius of their pores as x increased. The prepared bioceramic materials were mechanically characterized by means of Young’s modulus, flexural strength and fracture toughness measurements. The overall trend of these parameters evolved comparably to the relative density, and the maximum values obtained for x = 0.25 were measured to be 96 MPa, 47 MPa and 1.14 MPa·m^1/2, respectively.