Separation of Adsorbed and Intercalated Hydrazine in Hydrazine-Hydrate Intercalated Kaolinite by Controlled-Rate Thermal Analysis

Kristof, Janos, Frost, Ray L., Martens, Wayde N., & Horvath, Erzsebet (2002) Separation of Adsorbed and Intercalated Hydrazine in Hydrazine-Hydrate Intercalated Kaolinite by Controlled-Rate Thermal Analysis. Langmuir, 18(4), 1244 -1249.

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Abstract

The thermal behavior of a low-defect kaolinite fully expanded with hydrazine-hydrate has been investigated in a nitrogen atmosphere at a constant, preset decomposition rate of 0.15 mg/min. Under controlled-rate thermal analysis (CRTA) conditions, it was possible to distinguish between loosely bonded (adsorbed) and strongly bonded (intercalated) reagent. The loosely bonded reagent is connected to the internal and external surfaces of the expanded mineral and is present as a space filler between the sheets of the delaminated mineral. The strongly bonded hydrazine-hydrate is connected to the kaolinite inner-surface OH groups by the formation of hydrogen bonds. Based on the thermoanalytical results, three different types of bonded reagent could be distinguished in the complex. Type 1 reagent (approximately 0.20 mol hydrazine-hydrate/mol inner-surface OH) is liberated between approximately 50 and 70 C. Type 2 reagent is lost between approximately 70 and 85 C, corresponding to a quantity of 0.12-0.15 mol hydrazine-hydrate/mol inner-surface OH. Type 3 reagent is lost in the 85-130 C range, amounting to some 0.30 mol hydrazine/mol inner-surface OH. The quantity of this third type of reagent is independent of the conditions of sample pretreatment (drying). The liberation of bonded hydrazine-hydrate can be followed by FT-IR (DRIFT) spectroscopy in the OH and NH stretching ranges as well. When the complex is heated to 70 C under CRTA conditions, a new reflection appears in the XRD pattern with a d-value of 9.6 Å, in addition to the 10.3 Å reflection. This new reflection disappears in contact with moist air and the complex re-expands to the original d-value of 10.3 Å. The appearance of the 9.6 Å reflection is interpreted as the expansion of kaolinite with hydrazine alone, while the 10.3 Å one is due to expansion with hydrazine-hydrate.

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ID Code: 9867
Item Type: Journal Article
Refereed: Yes
Additional Information: This article is freely available from the American Chemical Society website 12 months after the publication date. See links to publisher website in this record.
DOI: 10.1021/la011179+
ISSN: 1520-5827
Divisions: Past > QUT Faculties & Divisions > Faculty of Science and Technology
Copyright Owner: Copyright 2002 American Chemical Society
Copyright Statement: The contents of this journal can be freely accessed online via the ACS web page 12 months after publication. See link to ACS website.
Deposited On: 02 Oct 2007 00:00
Last Modified: 10 Aug 2011 15:18

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