عنوان المقالة:Prediction of the metastable zone in “CaCO3-CO2-H2O” system Prediction of the metastable zone in “CaCO3-CO2-H2O” system
حمزة الفيل | Hamza Elfil | 3922
- نوع النشر
- مجلة علمية
- المؤلفون بالعربي
- حمزة الفيل، هونري روك
- المؤلفون بالإنجليزي
- Hamza Elfil, Henri Roques
- الملخص العربي
- The surpassing of the solubility product of the anhydrous forms of calcium carbonate calcite, aragonite, and vaterite is not sufficient to induce spontaneous precipitation. The existence of a metastable zone, in the nucleation of the calcium carbonate, is still an experimental phenomenon. A thermodynamic demarcation of the metastable zone in the “CaCO3–CO2–H2O” system, where only a secondary nucleation can occur, has been delimited for the first time. Through experimental exploration of a large supersaturation field, results obtained by the bubbling method are treated with the use of thermodynamic data of different varieties of CaCO3. At temperatures ranging between 25 and 60°C, a primary nucleation (spontaneous precipitation) occurs when the ionic activity product of the calco– carbonic solution surpasses the solubility product of CaCO3_H2O. No spontaneous nucleation occurs when the ionic activity product stabilizes between the solubility products of calcite and monohydrated calcium carbonate, which means that the solution remains in a metastable state. The metastability can be broken by seeding with calcium carbonate crystals (aragonite in this case) and then the germination is a secondary one. A model for the prediction of the limit of the metastable zone, presented in this report, is in agreement with experimental results.
- تاريخ النشر
- 24/08/2004
- الناشر
- AIChE Journal
- رقم المجلد
- 5
- رقم العدد
- 8
- رابط DOI
- DOI: 10.1002/aic.10160
- الصفحات
- 1908-1916
- رابط الملف
- تحميل (149 مرات التحميل)
- الكلمات المفتاحية
- metastability, secondary nucleation, crystallization, Monohydrated calcium carbonate, calcite