CO2 sequestration with serpentinite and metaperidotite from Northeast Portugal

被引:26
作者
Romao, Ines S. [1 ,2 ]
Gando-Ferreira, Licinio M. [2 ]
da Silva, M. Manuela V. G. [3 ,4 ]
Zevenhoven, Ron [1 ]
机构
[1] Abo Akad Univ, Thermal & Flow Engn Lab, Turku, Finland
[2] Univ Coimbra, Dept Chem Engn, Coimbra, Portugal
[3] Univ Coimbra, Dept Earth Sci, Coimbra, Portugal
[4] CEMUC, Coimbra, Portugal
基金
芬兰科学院;
关键词
CO2; sequestration; Mineral carbonation; Ammonium salts; Portugal; MAGNESIUM-SILICATE; MINERALIZATION; CARBONATION; SALTS;
D O I
10.1016/j.mineng.2016.05.009
中图分类号
TQ [化学工业];
学科分类号
0817 ;
摘要
The application of a staged process for CO2 sequestration by mineralisation, studied at Abo Akademi University (angstrom A), to abundant minerals from Northeast Portugal, is presented. Mg is extracted from magnesium silicates using recoverable ammonium salts (ammonium sulphate - AS and ammonium bisulphate - ABS), precipitated in the form of Mg(OH)(2) and subsequently carbonated at 20 bar CO2 partial pressure. The concept of the process is promising since the Mg extraction requires heat at similar to 450 degrees C while the Mg (OH)(2) carbonation produces heat at similar to 500 degrees C. Samples of serpentinite and metaperidotite were collected from Braganca and their theoretical capacity for CO2 mineralisation, in Northeast Portugal, was estimated to be 3.4 Gt of CO2. All the samples were mineralogically and physically characterized using X-ray diffraction and ICP-OES techniques and microscopic observation of thin sections. The reactivity of the samples, for Mg(OH)(2) production, was tested at different temperatures (350-500 degrees C) with AS and ABS, in different mixing conditions and both in the presence and absence of water. Metaperidotite was shown to be more reactive than serpentinite. The produced Mg(OH)(2) was carbonated in a pressurized fluidized bed at AA. The maximum Mg extraction (using ABS) and Mg(OH)(2) carbonation levels reached were 80% and 70%, respectively. (C) 2016 Elsevier Ltd. All rights reserved.
引用
收藏
页码:104 / 114
页数:11
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