Quantifying the effect of grain size on weathering of basaltic powders: Implications for negative emission technologies via soil carbon sequestration

IF 3.1 3区 地球科学 Q1 GEOCHEMISTRY & GEOPHYSICS Applied Geochemistry Pub Date : 2023-08-01 DOI:10.1016/j.apgeochem.2023.105728
Elizabeth Vanderkloot, Peter Ryan
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Abstract

Weathering of basaltic powders was studied experimentally at 35 °C in dilute solutions of oxalic acid and carbonic acid to assess the effect of grain size and reactive surface area for materials under consideration for carbon dioxide reduction (CDR) by enhanced rock weathering (ERW). The basalts chosen for this study (with their mineralogical compositions) are the Blue Ridge (BR) meta-basalt (chlorite > epidote > plagioclase > actinolite) and Pioneer Valley (PV) basalt (plagioclase > augite > quartz > chlorite). Powders of BR and PV basalts were sieved into <45 μ m, 45–150 μ m, and >150 μm fractions, and experiments were performed in open-system reactors designed to simulate a 1 mm thick layer of basalt added to agricultural soil in the humid tropics. Weathering rate was assessed by measuring the flux of base cations leached from silicate minerals and results indicate that silt-dominated basaltic powder (<45 μ m) weathers at approximately double the rate of sand dominated (150–500 μ m) basaltic powder, both for the BR and PV basalts. This study estimates CDR rates between 2.8 and 6.8 t CO2/ha/yr across the range of grain size fractions analyzed. Etched primary mineral grains (e.g. plagioclase, augite, actinolite) with depleted base cations observed by SEM-EDS provide morphological and stoichiometric evidence of dissolution, as do the presence of frayed chlorite grains that contain adsorbed Ca and are compositionally intermediate to end-member chlorite and smectite. Small amounts of micron-scale calcite were also observed as a precipitate on mineral surfaces, likely a consequence of localized saturation of Ca and HCO3 in the matrix of the weathering powders. The results of this study help to constrain differences in weathering flux as a function of grain size, with important implications for effectiveness of CDR via ERW.

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量化粒度对玄武岩粉末风化的影响:通过土壤碳固存对负排放技术的影响
研究了玄武岩粉末在35°C的稀草酸和碳酸溶液中的风化作用,考察了晶粒尺寸和活性表面积对增强岩石风化法(ERW)二氧化碳还原(CDR)材料的影响。本研究选择的玄武岩(及其矿物组成)为蓝岭(BR)变质玄武岩(绿泥石>绿帘石比;斜长石比;放线石)和先锋谷(PV)玄武岩(斜长石);辉石比;石英比;绿泥石)。将BR和PV玄武岩粉末筛分成45 μm、45 - 150 μm和150 μm馏分,在开放系统反应器中模拟在湿润热带地区农业土壤中添加1 mm厚的玄武岩层。通过测量硅酸盐矿物浸出的碱阳离子通量来评估风化速率,结果表明,粉质占主导地位的玄武岩粉(<45 μ m)的风化速率大约是砂质占主导地位的玄武岩粉(150 ~ 500 μ m)的两倍。本研究估计,在所分析的颗粒级分数范围内,CDR率在2.8至6.8吨二氧化碳/公顷/年之间。扫描电镜-能谱仪观察到,碱离子耗尽的原生矿物颗粒(如斜长石、辉长石、放光石)被蚀刻,提供了溶解的形态和化学计量学证据,同时也提供了含有吸附Ca的磨损绿泥石颗粒的存在,这些颗粒的成分介于端元绿泥石和蒙脱石之间。少量的微米级方解石也被观察到作为矿物表面的沉淀,可能是风化粉末基质中Ca和HCO3局部饱和的结果。本研究结果有助于约束风化通量随粒径的差异,对通过ERW进行CDR的有效性具有重要意义。
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来源期刊
Applied Geochemistry
Applied Geochemistry 地学-地球化学与地球物理
CiteScore
6.10
自引率
8.80%
发文量
272
审稿时长
65 days
期刊介绍: Applied Geochemistry is an international journal devoted to publication of original research papers, rapid research communications and selected review papers in geochemistry and urban geochemistry which have some practical application to an aspect of human endeavour, such as the preservation of the environment, health, waste disposal and the search for resources. Papers on applications of inorganic, organic and isotope geochemistry and geochemical processes are therefore welcome provided they meet the main criterion. Spatial and temporal monitoring case studies are only of interest to our international readership if they present new ideas of broad application. Topics covered include: (1) Environmental geochemistry (including natural and anthropogenic aspects, and protection and remediation strategies); (2) Hydrogeochemistry (surface and groundwater); (3) Medical (urban) geochemistry; (4) The search for energy resources (in particular unconventional oil and gas or emerging metal resources); (5) Energy exploitation (in particular geothermal energy and CCS); (6) Upgrading of energy and mineral resources where there is a direct geochemical application; and (7) Waste disposal, including nuclear waste disposal.
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