含水层
溶解有机碳
铀
化学
地下水
有机质
环境化学
浸出(土壤学)
傅里叶变换离子回旋共振
质谱法
地质学
土壤科学
土壤水分
色谱法
有机化学
冶金
岩土工程
材料科学
作者
Chongsheng Lu,Wei Xiu,Bing Yang,Guoxi Lian,Tianjing Zhang,Erping Bi,Huaming Guo
摘要
Abstract Dissolved organic matter (DOM) is widespread in uranium (U) hosting aquifer, a key substance affecting CO 2 + O 2 in situ leaching (ISL) of U by consuming injected O 2 . However, molecular composition and molecular transformation of DOM are poorly understood in this aquifer during the U mining. To address this issue, Fourier transform ion cyclotron resonance mass spectrometry was applied to investigate DOM molecules in groundwater samples and rock samples collected from a U mining aquifer. The high proportion of labile tyrosine‐like component and BIX value in monitoring wells (BM) indicated the biological origin of DOM. CHOS and aliphatic were the major components of water‐soluble organic matter (WSOM) in U‐bearing rocks, but CHO and highly unsaturated structures with high oxygen (HUSHO) were the main components of DOM in BM. The ISL led to the release of WSOM and the oxidation of DOM, which accounted for 24.5%–57.4% and 39.1%–65.7% of expected DOM, respectively. Potential molecular transformations (PMTs) results showed that the intragroup transformations dominated, and remarkable transformations from CHON and CHONS to CHO occurred during ISL. The positive net PMTs of condensed aromatic structure (CAS), aromatic structures (AS), and aliphatic suggested that they were transformed from HUSLO and HUSHO. A gradual decrease in (DBE−O)/C wa and a gradual increase in NOSC wa indicated that the saturated degree and oxidation state of DOM increased during mining. This work successfully identified molecular characteristics of DOM in U hosting aquifer, and proposed a paradigm of DOM transformation pathways during ISL.
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