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Clathrate Hydrates for Production of Potable Water

Published online by Cambridge University Press:  01 February 2011

Robert W. Bradshaw
Affiliation:
rwbrads@sandia.gov, Sandia National Labs, Materials Chemistry, PO Box 969, MS9403, Livermore, 94551-0969, United States, 925-294-3229
Blake A. Simmons
Affiliation:
basimmo@sandia.gov, Sandia National Labs, Nano-Scale Science & Tech, PO Box 969, MS9161, Livermore, 94551-0969, United States
Eric H Majzoub
Affiliation:
ehmajzo@sandia.gov, Sandia National Labs, Analytical Materials Science, PO Box 969, MS9402, Livermore, 94551-0969, United States
W. Miles Clift
Affiliation:
wmclift@sandia.gov, Sandia National Labs, Analytical Materials Science, PO Box 969, MS9402, Livermore, 94551-0969, United States
Daniel E. Dedrick
Affiliation:
dedrick@sandia.gov, Sandia National Labs, Thermal/Fluid Science & Engr, PO Box 969, MS9409, Livermore, 94551-0969, United States
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Abstract

Clathrate hydrates are crystalline inclusion compounds of water and a guest molecule (e.g., methane) that form at temperatures below ambient but above the freezing point of water. There are three known crystalline structures of hydrates (structure I, II, and H) in which cavities within the hydrogen bonded water molecule lattice trap the hydrate-forming species. The clathrate structure excludes dissolved solutes, such as sodium chloride, from the aqueous phase and thereby offers a possible means to produce potable water from seawater or brackish water. The concept of using clathrate hydrates for desalination is not new. However, before clathrate hydrate desalination becomes a viable technology, fundamental issues of controlled hydrate formation, hydrate size and morphology, agglomeration, amount of entrapped salt, and the efficient recovery of hydrates must be understood. This paper will report structural characterization of hydrates formed with several guest molecules over a wide range of conditions in an attempt to further the physicochemical insight needed to address these issues.

Clathrate hydrate formation experiments were performed using a variety of host molecules, including R141b, a commercial refrigerant, C2FCl2H3. Hydrates of R141b were formed at temperatures from 2°C to 6°C and atmospheric pressure from deionized water and 2% - 7% NaCl solutions. Samples of the hydrates were characterized by cold-stage x-ray diffraction and Raman spectroscopy and determined to be structure II. Additional experiments were conducted with a gaseous hydrate former, ethylene, which readily formed hydrates with deionized or saline water at 2°C and several atmospheres of pressure. Experiments with several other hydrate forming molecules were conducted and the results obtained from their structural characterization will be reported. We will also present proof-of-concept experiments demonstrating a novel technique of desalination using these hydrate formers.

Sandia National Laboratories is a multiprogram laboratory operated by Sandia Corporation, a Lockheed Martin company, for the United States Department of Energy under contract DE-AC04-94AL85000.

Type
Research Article
Copyright
Copyright © Materials Research Society 2006

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