Bioleaching
Bioleaching is a biotechnological hydrometallurgical process that utilizes acidophilic microorganisms to oxidize insoluble metal sulfides in ores, converting them into soluble metal ions through the production of ferric iron and sulfuric acid as oxidizing and complexing agents.[1][2] This method enables the extraction of valuable metals such as copper, uranium, gold, and zinc from low-grade or refractory ores where traditional smelting or roasting is inefficient or prohibitively costly due to high energy demands and emissions.[3][4] The primary microorganisms involved, including Acidithiobacillus ferrooxidans and Leptospirillum ferriphilum, thrive in acidic environments (pH 1-3) and catalyze indirect leaching by regenerating ferric ions from ferrous iron, alongside direct enzymatic attack on mineral lattices.[1][5] Industrial applications, operational since the mid-20th century, predominantly employ heap, dump, and in situ leaching configurations for copper recovery, contributing to 10-20% of global production from sulfide ores, with extraction efficiencies often exceeding 80% under optimized conditions.[6][7] Emerging uses extend to rare earth elements, e-waste, and battery recycling, leveraging bioleaching's lower capital costs and reduced greenhouse gas emissions compared to pyrometallurgy, though process durations can span months, posing scalability challenges.[8][9] Despite its environmental advantages—such as minimal land disturbance and avoidance of high-temperature processing—bioleaching generates acidic leachates requiring neutralization to mitigate risks of acid mine drainage, and microbial inhibition by high metal concentrations or toxins remains a key limitation addressed through strain engineering and process intensification.[10][11] Pioneered in uranium extraction during the 1950s and scaled for copper in Chile and South Africa, bioleaching exemplifies causal integration of microbial metabolism with geochemical cycles for resource recovery, with ongoing research enhancing yields via genetic modifications and hybrid physico-chemical approaches.[6][12]