Ferrini Vincenzo, De Vito Caterina, Mignardi Silvano
Dipartimento di Scienze della Terra, Università degli Studi di Roma La Sapienza, 00185 Roma, Italy.
J Hazard Mater. 2009 Sep 15;168(2-3):832-7. doi: 10.1016/j.jhazmat.2009.02.103. Epub 2009 Feb 26.
In this paper is reported a novel method to synthesize nesquehonite, MgCO(3) x 3H(2)O, via reaction of a flux of CO(2) with Mg chloride solution at 20+/-2 degrees C. The reaction rate is rapid, with carbonate deposition almost complete in about 10 min. The full characterization of the product of synthesis has been performed to investigate its potential role as a "CO(2)-sequestering medium" and a means of disposing Mg-rich wastewater. We investigated the nesquehonite synthesized using SEM, XRD, FTIR and thermal analysis. The thermodynamic and chemical stability of this low-temperature hydrated carbonate of Mg and its possible transformation products make our method a promising complementary solution to other methods of CO(2) sequestration. Carbonation via magnesium chloride aqueous solutions at standard conditions represents a simple and permanent method of trapping CO(2). It could be applied at point sources of CO(2) emission and could involve rejected brine from desalination plants and other saline aqueous wastes (i.e., "produced water"). The likelihood of using the resulting nesquehonite and the by-products of the process in a large number of applications makes our method an even more attractive solution.
本文报道了一种通过在20±2℃下使二氧化碳流与氯化镁溶液反应来合成三水碳酸镁(MgCO₃·3H₂O)的新方法。反应速率很快,约10分钟内碳酸盐沉积几乎完成。对合成产物进行了全面表征,以研究其作为“二氧化碳封存介质”的潜在作用以及处理富镁废水的一种手段。我们使用扫描电子显微镜(SEM)、X射线衍射仪(XRD)、傅里叶变换红外光谱仪(FTIR)和热分析对合成的三水碳酸镁进行了研究。这种镁的低温水合碳酸盐及其可能的转化产物的热力学和化学稳定性使我们的方法成为其他二氧化碳封存方法的一种有前景的补充解决方案。在标准条件下通过氯化镁水溶液进行碳酸化是一种简单且永久的捕获二氧化碳的方法。它可应用于二氧化碳排放的点源,并且可能涉及来自海水淡化厂的废盐水和其他含盐废水(即“采出水”)。在大量应用中使用所得三水碳酸镁及该过程副产物的可能性使我们的方法成为更具吸引力的解决方案。