The present disclosure broadly relates to a process for recovering magnesium as magnesium oxide and fibrous amorphous silica from serpentinite feedstocks. More specifically, but not exclusively, the present disclosure relates to metallurgical and chemical processes for recovering magnesium oxide and fibrous amorphous silica from serpentinite feedstocks. The process broadly comprises applying a sufficient amount of shear deformation force to the serpentine feedstocks to produce a particulate material of reduced size; subjecting the particulate material to magnetic separation to produce a primary magnetic separation product and iron-reduced tailings; and digesting the iron-reduced tailings into nitric acid, producing a magnesium-rich pregnant solution and insoluble solids. The process further comprises adjusting the pH of the pregnant solution to values ranging from about 5.0 to about 7.0.

An improved beta(?)-spodumene (?LiAlSi.sub.2O.sub.6) nitric acid conversion process produces discrete lithium (Li), aluminum (Al) and silica (SiO.sub.2) materials by: (i) converting lithium nitrate, LiNO.sub.3, to lithium carbonate, Li.sub.2CO.sub.3; (ii) creating a Al-rich precipitate either by thermally decomposing aluminum nitrate, Al(NO.sub.3).sub.3, or by reacting Al(NO.sub.3).sub.3 with aqueous and/or solid ammonium carbonate, (NH.sub.4).sub.2CO.sub.3; and (iii) forming a solid SiO.sub.2-rich aluminosilicate residue by selectively leaching Li and Al from ?-spodumene. Three key reactants consumed during processingnitric acid (HNO.sub.3), ammonia (NH.sub.3), and magnesium oxide (MgO)may be regenerated internally by closed-loop chemical cycles, this feature of the process greatly improving its economics in commercial applications.

An improved beta(?)-spodumene (?LiAlSi.sub.2O.sub.6) nitric acid conversion process produces discrete lithium (Li), aluminum (Al) and silica (SiO.sub.2) materials by: (i) converting lithium nitrate, LiNO.sub.3, to lithium carbonate, Li.sub.2CO.sub.3; (ii) creating a Al-rich precipitate either by thermally decomposing aluminum nitrate, Al(NO.sub.3).sub.3, or by reacting Al(NO.sub.3).sub.3 with aqueous and/or solid ammonium carbonate, (NH.sub.4).sub.2CO.sub.3; and (iii) forming a solid SiO.sub.2-rich aluminosilicate residue by selectively leaching Li and Al from ?-spodumene. Three key reactants consumed during processingnitric acid (HNO.sub.3), ammonia (NH.sub.3), and magnesium oxide (MgO)may be regenerated internally by closed-loop chemical cycles, this feature of the process greatly improving its economics in commercial applications.

An improved beta(?)-spodumene (?LiAlSi.sub.2O.sub.6) nitric acid conversion process produces discrete lithium (Li), aluminum (Al) and silica (SiO.sub.2) materials by: (i) converting lithium nitrate, LiNO.sub.3, to lithium carbonate, Li.sub.2CO.sub.3; (ii) creating a Al-rich precipitate either by thermally decomposing aluminum nitrate, Al(NO.sub.3).sub.3, or by reacting Al(NO.sub.3).sub.3 with aqueous and/or solid ammonium carbonate, (NH.sub.4).sub.2CO.sub.3; and (iii) forming a solid SiO.sub.2-rich aluminosilicate residue by selectively leaching Li and Al from ?-spodumene. Three key reactants consumed during processingnitric acid (HNO.sub.3), ammonia (NH.sub.3), and magnesium oxide (MgO)may be regenerated internally by closed-loop chemical cycles, this feature of the process greatly improving its economics in commercial applications.

An improved beta(?)-spodumene (?LiAlSi.sub.2O.sub.6) nitric acid conversion process produces discrete lithium (Li), aluminum (Al) and silica (SiO.sub.2) materials by: (i) converting lithium nitrate, LiNO.sub.3, to lithium carbonate, Li.sub.2CO.sub.3; (ii) creating a Al-rich precipitate either by thermally decomposing aluminum nitrate, Al(NO.sub.3).sub.3, or by reacting Al(NO.sub.3).sub.3 with aqueous and/or solid ammonium carbonate, (NH.sub.4).sub.2CO.sub.3; and (iii) forming a solid SiO.sub.2-rich aluminosilicate residue by selectively leaching Li and Al from ?-spodumene. Three key reactants consumed during processingnitric acid (HNO.sub.3), ammonia (NH.sub.3), and magnesium oxide (MgO)may be regenerated internally by closed-loop chemical cycles, this feature of the process greatly improving its economics in commercial applications.

A method of manufacturing a nanocomposite may include combining a magnesium salt, an aluminum salt, and a ferric salt in stoichiometric proportions within 5 mol. % in an aqueous solvent including menthol or dextrose, to obtain a first mixture, heating the first mixture to remove at least 99.5 wt. % of the aqueous solvent to obtain a first solid, grinding the first solid into a first powder, calcining the first powder at a temperature of about 600 C. to 800 C. for a time of about 2 to 4 hours to obtain a second solid, grinding the second solid and urea, in an amount sufficient to form the nanocomposite, into a second powder, heating the second powder at a temperature of about 550 C. to 650 C. for a time of about 15 minutes to 1.5 hours to obtain the nanocomposite.

A method of manufacturing a nanocomposite may include combining a magnesium salt, an aluminum salt, and a ferric salt in stoichiometric proportions within 5 mol. % in an aqueous solvent including menthol or dextrose, to obtain a first mixture, heating the first mixture to remove at least 99.5 wt. % of the aqueous solvent to obtain a first solid, grinding the first solid into a first powder, calcining the first powder at a temperature of about 600 C. to 800 C. for a time of about 2 to 4 hours to obtain a second solid, grinding the second solid and urea, in an amount sufficient to form the nanocomposite, into a second powder, heating the second powder at a temperature of about 550 C. to 650 C. for a time of about 15 minutes to 1.5 hours to obtain the nanocomposite.