Thermal analyis of hexadecyltrimethylammonium–montmorillonites: Part 1. Thermogravimetry, carbon and hydrogen analysis and thermo-IR spectroscopy analysis
Na-montmorillonite (Na-MONT) was loaded with hexadecyltrimethylammonium cations (HDTMA) by replacing 41 and 90% of the exchangeable Na with HDTMA, labeled OC-41 and OC-90, respectively. Na-MONT, OC-41, and OC-90 were heated in air up to 900 °C. Unheated and thermally treated organoclays heated at 15...
Gespeichert in:
Veröffentlicht in: | Journal of thermal analysis and calorimetry 2011-09, Vol.105 (3), p.921-929 |
---|---|
Hauptverfasser: | , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
Zusammenfassung: | Na-montmorillonite (Na-MONT) was loaded with hexadecyltrimethylammonium cations (HDTMA) by replacing 41 and 90% of the exchangeable Na with HDTMA, labeled OC-41 and OC-90, respectively. Na-MONT, OC-41, and OC-90 were heated in air up to 900 °C. Unheated and thermally treated organoclays heated at 150, 250, 360, and 420 °C are used in our laboratory as sorbents of different hazardous organic compounds from waste water. In order to get a better knowledge about the composition and nature of the thermally treated organoclays Na-MONT and the two organo-clays were studied by thermogravimetry (TG) in air and under nitrogen. Carbon and hydrogen contents in each of the thermal treated sample were determined and their infrared spectra were recorded. The present results showed that at 150 °C both organoclays lost water but not intercalated HDTMA cations. At 250 °C, many HDTMA cations persisted in OC-41, but in OC-90 significant part of the cations were air-oxidized into H
2
O and CO
2
and the residual carbon formed charcoal. After heating both samples at 360 °C charcoal was present in both organo clays. This charcoal persisted at 420 °C but was gradually oxidized by air with further rise in temperature. TG runs under nitrogen showed stepwise degradation corresponding to interlayer water desorption followed by decomposition of the organic compound, volatilization of small fragments and condensation of non-volatile fragments into quasi-charcoal. After dehydroxylation of the clay the last stages of organic matter pyrolysis and volatilization occurred. |
---|---|
ISSN: | 1388-6150 1588-2926 1572-8943 |
DOI: | 10.1007/s10973-011-1304-4 |