The precipitation of different forms of magnesium carbonate has been studied at temperatures between 25 and 120 {ring operator} C and at a partial pressure of CO2 between 1 and 100 bar. These conditions are relevant for mineral carbonation applications. Precipitation was triggered by the supersaturation created by mixing Na2CO3 solutions in equilibrium with a CO2 atmosphere with MgCl2 solutions. Experiments were monitored using attenuated total reflection Fourier transform infrared (ATR-FTIR) and Raman spectroscopy as well as a focused beam reflectance measurement (FBRM) probe and a turbidimeter. Solubility and supersaturation were calculated using the software package EQ3/6. Solids were identified using X-ray diffraction (XRD) analysis and scanning electron microscope (SEM) images. At 25 {ring operator} C and PCO2 = 1 bar, only the hydrated carbonate nesquehonite (MgCO3 · 3 H2 O) precipitates, as it has previously been observed. Solutions undersaturated with respect to nesquehonite did not form any precipitates in experiments lasting 16 h. Induction times increased with decreasing supersaturation with respect to nesquehonite. At 120 {ring operator} C and PCO2 = 3 bar, hydromagnesite ((MgCO3)4 · Mg (OH)2 · 4 H2 O) was formed which transformed within 5-15 h into magnesite (MgCO3). Solutions undersaturated with respect to brucite (Mg(OH)2) did not form any precipitates in experiments lasting 19 h. At 120 {ring operator} C and PCO2 = 100 bar, direct formation of magnesite and, at elevated levels of supersaturation, the co-precipitation of magnesite and hydromagnesite has been observed. In the latter case, hydromagnesite transformed within a few hours into magnesite. Solutions undersaturated with respect to hydromagnesite did not form any precipitates in experiments lasting 20 h. © 2007 Elsevier Ltd. All rights reserved.
Precipitation in the Mg-carbonate system-effects of temperature and CO2 pressure
Prigiobbe V.;
2008
Abstract
The precipitation of different forms of magnesium carbonate has been studied at temperatures between 25 and 120 {ring operator} C and at a partial pressure of CO2 between 1 and 100 bar. These conditions are relevant for mineral carbonation applications. Precipitation was triggered by the supersaturation created by mixing Na2CO3 solutions in equilibrium with a CO2 atmosphere with MgCl2 solutions. Experiments were monitored using attenuated total reflection Fourier transform infrared (ATR-FTIR) and Raman spectroscopy as well as a focused beam reflectance measurement (FBRM) probe and a turbidimeter. Solubility and supersaturation were calculated using the software package EQ3/6. Solids were identified using X-ray diffraction (XRD) analysis and scanning electron microscope (SEM) images. At 25 {ring operator} C and PCO2 = 1 bar, only the hydrated carbonate nesquehonite (MgCO3 · 3 H2 O) precipitates, as it has previously been observed. Solutions undersaturated with respect to nesquehonite did not form any precipitates in experiments lasting 16 h. Induction times increased with decreasing supersaturation with respect to nesquehonite. At 120 {ring operator} C and PCO2 = 3 bar, hydromagnesite ((MgCO3)4 · Mg (OH)2 · 4 H2 O) was formed which transformed within 5-15 h into magnesite (MgCO3). Solutions undersaturated with respect to brucite (Mg(OH)2) did not form any precipitates in experiments lasting 19 h. At 120 {ring operator} C and PCO2 = 100 bar, direct formation of magnesite and, at elevated levels of supersaturation, the co-precipitation of magnesite and hydromagnesite has been observed. In the latter case, hydromagnesite transformed within a few hours into magnesite. Solutions undersaturated with respect to hydromagnesite did not form any precipitates in experiments lasting 20 h. © 2007 Elsevier Ltd. All rights reserved.Pubblicazioni consigliate
I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.