Uraninite alteration / Uranyl phosphates / Uranyl sulfates / E h -pH diagrams / Natural fission reactor / Oklo / BangombéSummary. The mineralogy of the supergene-weathered Bangombé natural fission reactor (RZB) and surrounding uranium deposit has been analyzed and compared with the thermodynamically predicted minerals based on groundwater compositions. The primary U-minerals are uraninite UO 2+x and minor coffinite (U[SiO 4 ]·nH 2 O); sometimes with phosphorous. The U 6+ miner-has also been reported. Thermodynamic equilibrium modeling was completed using Geochemist's Workbench with an expanded data base and the groundwater composition (−112 mV ≤ E h ≤ 143 mV; pH = 5.96) at the base of RZB in drill-hole BAX03. The new ∆G 0 f, 298.15 data were obtained from the literature or estimated using the polyhedral contribution method. Based on the updated database, E h −pH diagrams predict that coffinite, U(HPO 4 ) 2 ·H 2 O and UOF 2 ·H 2 O are the only stable U 4+ phases and that uranopilite, torbernite and bassetite will become stable during oxidative alteration. Except from UOF 2 ·H 2 O, this is in accord with mineralogical observations. The role of Cu was predicted from log a Cu -pH diagrams, which predicts that torbernite is stable at log a Cu = 3.98 × 10 −14 and pH ≥ 2.2 at E h = 143 mV in BAX03 groundwaters. At E h = −112 mV, torbernite is stable at pH > 5.5. Soddyite ((UO 2 ) 2 SiO 4 ·2H 2 O) was predicted to form at the expense of coffinite, but soddyite has not been identified at Bangombé. Previous blind prediction modeling, often omitting P and S, had only predicted soddyite and haiweeite (Ca(UO 2 ) 2 [Si 5 O 12 (OH) 2 ]·4−5H 2 O) and hence, failed to predict the U 6+ minerals observed at Bangombé. The results stress the importance of SO 4 2− and PO 4 3− resulting from dissolution of accessory apatite, monazite and sulfides in the retardation of U owing to the formation of U 6+ sulfates and phosphates.