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A study on MgO-based mineral carbonation kinetics using pressurised thermo-gravimetric analysis

机译:加压热重分析法研究基于MgO的矿物碳酸化动力学

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The carbonation of magnesium silicate mineral appears to be the only option for CO_2 capture and storage (CCS) in Finland. Current research in Finland focuses on the carbonation of silicate minerals and industrial wastes such as slag from iron and steel plants, using both dry (gas/solid) and wet (aqueous solution) methods. The kinetics of MgO (periclase) and Mg(OH)_2 (brucite) particle (75-125 μm) carbonation at temperatures and pressures up to 540°C and 45 bar was measured using pressurised thermogravimetric analysis. Conversion levels of 40 to 60 % after 6 h were obtained. Unreacted shrinking core (USC) modelling allowed for calculating initial reaction rates, showing also that intra-particle diffusion through presumably a MgCO_3 (magnesite) product layer becomes rate-determining after ~5 % conversion.
机译:硅酸镁矿物的碳酸化似乎是芬兰CO_2捕集与封存(CCS)的唯一选择。芬兰目前的研究重点是使用干法(气体/固体)和湿法(水溶液)将硅酸盐矿物和工业废料(如钢铁厂的炉渣)碳化。使用加压热重分析法测量了在高达540°C和45 bar的温度和压力下MgO(过氧化物酶)和Mg(OH)_2(青石)颗粒(75-125μm)碳化的动力学。 6小时后转化率为40%到60%。未反应的收缩核(USC)模型可用于计算初始反应速率,也表明颗粒内通过大概MgCO_3(菱镁矿)产品层的扩散在转化率约为5%之后成为速率确定的。

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