Comparing the reactivity of different natural clays under thermal and alkali activation
Auteur(s): |
Ahmed Zohair Khalifa
Yiannis Pontikes Jan Elsen Özlem Cizer |
---|---|
Médium: | article de revue |
Langue(s): | anglais |
Publié dans: | RILEM Technical Letters, février 2020, v. 4 |
Page(s): | 74-80 |
DOI: | 10.21809/rilemtechlett.2019.85 |
Abstrait: |
Metakaolin is one of the most popular solid aluminosilicate precursors for the synthesis of geopolymers. Despite its high reactivity and availability, there is a noticeable move towards the use of other natural clays as alternative precursors, due to their plentiful supply and widespread availability. Natural clays usually consist of a combination of 1:1 and 2:1 layer silicates reactivity of which vary. In this work, four different natural clays (SS, BS, MS and WS) composed of 1:1 and 2:1 clay minerals at different proportions were studied for the synthesis of geopolymers. To increase their reactivity prior to alkali activation, the clays were calcined in a laboratory oven at different temperatures (700, 750, 800, 850, 900 °C) and different holding times (10 seconds to 60 minutes). The reactivity of the calcined clays was assessed by the dissolution test and isothermal conduction calorimetry. NaOH and a mix of NaOH and Na2SiO3 were used as alkaline activators. The results show that the optimum calcination temperature of SS, BS and MS is 800 °C with a holding time of 10 minutes. WS is sufficiently calcined at a higher temperature of 900 °C for 20 minutes. Kaolinite-rich clays (SS) present more reactivity towards alkali activation than clays dominated by smectite or illite. |
License: | Cette oeuvre a été publiée sous la license Creative Commons Attribution 4.0 (CC-BY 4.0). Il est autorisé de partager et adapter l'oeuvre tant que l'auteur est crédité et la license est indiquée (avec le lien ci-dessus). Vous devez aussi indiquer si des changements on été fait vis-à-vis de l'original. |
1.2 MB
- Informations
sur cette fiche - Reference-ID
10412154 - Publié(e) le:
08.02.2020 - Modifié(e) le:
02.06.2021