CO2 Hydrate:  Synthesis, Composition, Structure, Dissociation Behavior, and a Comparison to Structure I CH4 Hydrate

水合物 笼状水合物 离解(化学) 甲烷 微晶 熔点 化学 分析化学(期刊) 相界 材料科学 结晶学 相(物质) 物理化学 色谱法 有机化学
作者
Susan Circone,Laura A. Stern,S. H. Kirby,W. B. Durham,Bryan C. Chakoumakos,Claudia J. Rawn,Adam J. Rondinone,Yoshinobu Ishii
出处
期刊:Journal of Physical Chemistry B [American Chemical Society]
卷期号:107 (23): 5529-5539 被引量:234
标识
DOI:10.1021/jp027391j
摘要

Structure I (sI) carbon dioxide (CO2) hydrate exhibits markedly different dissociation behavior from sI methane (CH4) hydrate in experiments in which equilibrated samples at 0.1 MPa are heated isobarically at 13 K/h from 210 K through the H2O melting point (273.15 K). The CO2 hydrate samples release only about 3% of their gas content up to temperatures of 240 K, which is 22 K above the hydrate phase boundary. Up to 20% is released by 270 K, and the remaining CO2 is released at 271.0 ± 0.5 K, where the sample temperature is buffered until hydrate dissociation ceases. This reproducible buffering temperature for the dissociation reaction CO2·nH2O = CO2(g) + nH2O(l to s) is measurably distinct from the pure H2O melting point at 273.15 K, which is reached as gas evolution ceases. In contrast, when sI CH4 hydrate is heated at the same rate at 0.1 MPa, >95% of the gas is released within 25 K of the equilibrium temperature (193 K at 0.1 MPa). In conjunction with the dissociation study, a method for efficient and reproducible synthesis of pure polycrystalline CO2 hydrate with suitable characteristics for material properties testing was developed, and the material was characterized. CO2 hydrate was synthesized from CO2 liquid and H2O solid and liquid reactants at pressures between 5 and 25 MPa and temperatures between 250 and 281 K. Scanning electron microscopy (SEM) examination indicates that the samples consist of dense crystalline hydrate and 50−300 μm diameter pores that are lined with euhedral cubic hydrate crystals. Deuterated hydrate samples made by this same procedure were analyzed by neutron diffraction at temperatures between 4 and 215 K; results confirm that complete conversion of water to hydrate has occurred and that the measured unit cell parameter and thermal expansion are consistent with previously reported values. On the basis of measured weight gain after synthesis and gas yields from the dissociation experiments, approximately all cages in the hydrate structure are filled such that n ≈ 5.75.
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