Nanoscale mineralogical evolution of pyrite and secondary phases during and after spontaneous coal combustion in coal reject deposits.

IF 4.2 3区 环境科学与生态学 Q1 CHEMISTRY, ANALYTICAL Environmental Science: Processes & Impacts Pub Date : 2026-10-15 DOI:10.1039/d6em00572a
Luis F O Silva, Tito J Crissien, Marcos L S Oliveira, Tobias K Misicko, Xiao-Ying Yu, Sisara Samaradiwakara, Michael Schindler
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Abstract

Spontaneous coal combustion (SCC) occurs globally and releases particulate matter, acid gases (e.g., SO2 and NOx), and metals into the environment. This study characterizes nanometer-scale processes that occur during and after SCC in Urussanga, Santa Catarina, Brazil. A multi-analytical approach using various surface- and electron-microscopy techniques allowed the identification of secondary mineral processes and the formation of secondary minerals. Weathering of thermally altered pyrite and coal rejects forms secondary weathering crusts composed predominantly of Fe-oxides (hematite and spinel-group minerals), amorphous silica, clay minerals (illite-smectite, I-S, and kaolinite), sulfides (pyrite), and sulfates (gypsum and jarosite-alunite group minerals). The crusts are enriched in metals common in pyrite, form efflorescent minerals, or show high structural compatibility with Fe-oxides. Pyrite transforms into pyrrhotite, mikasaite, Fe2(SO4)3, and hematite under different O2 and hydrocarbon activities. Porous coal matrices allowed inferred meteoric water to infiltrate pyrite-coal-clay mineral associations. This promoted the non-stoichiometric dissolution of I-S into amorphous silica and the weathering of pyrite to nanometer-thick secondary Fe-sulfate layers in confined pore spaces along pyrite-coal interfaces. The high abundance of clay minerals and amorphous silica resulted in the entrapment/armoring of pyrite-, TiO2-, and jarosite-alunite nanoparticles and the heterogeneous nucleation of jarosite on the (001) basal surface of kaolinite. These findings indicate complex interactions between the original minerals in coal rejects (pyrite and I-S), thermal alteration products (pyrrhotite, mikasaite, and TiO2), and post-combustion weathering products (amorphous silica, Fe-sulfates and -(hydr)oxides), as well as the geochemical redistribution of environmentally significant elements during and after SCC.

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矸石煤自燃过程中及燃烧后黄铁矿及次生相的纳米级矿物学演化。
煤炭自燃(SCC)在全球范围内发生,并向环境中释放颗粒物、酸性气体(如二氧化硫和氮氧化物)和金属。本研究表征了在巴西圣卡塔琳娜州乌鲁桑加发生的SCC期间和之后的纳米尺度过程。使用各种表面和电子显微镜技术的多分析方法可以识别次生矿物过程和次生矿物的形成。热蚀黄铁矿和煤矸石风化形成次生风化壳,主要由铁氧化物(赤铁矿和尖晶石群矿物)、无定形二氧化硅、粘土矿物(伊利石-蒙脱石、I-S和高岭石)、硫化物(黄铁矿)和硫酸盐(石膏和黄钾矾石-明矾石群矿物)组成。地壳富含黄铁矿中常见的金属,形成荧光矿物,或与铁氧化物具有较高的结构相容性。黄铁矿在不同的O2和烃类活性下转化为磁黄铁矿、辉kasaite、Fe2(SO4)3和赤铁矿。多孔煤基质允许推断的大气水渗透到黄铁矿-煤-粘土矿物组合中。这促进了I-S在无定形二氧化硅中的非化学计量溶解,并促进了黄铁矿沿黄铁矿-煤界面在密闭孔隙中风化成纳米厚的次生硫酸铁层。高丰度的粘土矿物和无定形二氧化硅导致黄铁矿-、TiO2-和黄钾铁矾-明矾纳米颗粒的包裹/装甲,以及黄钾铁矾在高岭石(001)基表面的非均质成核。这些发现表明,煤渣中的原始矿物(黄铁矿和硫化物)、热蚀变产物(磁黄铁矿、云母铁矿和TiO2)和燃烧后风化产物(无定形二氧化硅、铁硫酸盐和-(氢)氧化物)之间存在复杂的相互作用,以及SCC期间和之后环境重要元素的地球化学再分配。
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来源期刊
Environmental Science: Processes & Impacts
Environmental Science: Processes & Impacts CHEMISTRY, ANALYTICAL-ENVIRONMENTAL SCIENCES
CiteScore
9.50
自引率
3.60%
发文量
202
审稿时长
1 months
期刊介绍: Environmental Science: Processes & Impacts publishes high quality papers in all areas of the environmental chemical sciences, including chemistry of the air, water, soil and sediment. We welcome studies on the environmental fate and effects of anthropogenic and naturally occurring contaminants, both chemical and microbiological, as well as related natural element cycling processes.
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High roughness and porosity of indoor surfaces increases sorption capacity and may impact indoor air quality. Evaluating emission rate estimation methods for ecological exposure and safety assessment: a case study for cyclic volatile methyl siloxanes. Nanoscale mineralogical evolution of pyrite and secondary phases during and after spontaneous coal combustion in coal reject deposits. Water quality assessment in two agricultural streams in the pampas region, Argentina: an integrated landscape, physicochemical, chemical, and ecotoxicological approach. A mechanistic model for gas transfer velocity in the Damodar river.
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