Ana Rita C. Duarte

Phase equilibrium measurements of single and mixed organic clathrate hydrates with hydrogen were determined within a pressure range of 2.0-14.0. MPa. The organic compounds studied were furan, 2,5-dihydrofuran, tetrahydropyran, 1,3-dioxolane and cyclopentane. These organic compounds are known to form structure II clathrate hydrates with water. It was found that the addition of hydrogen to form a mixed clathrate hydrate increases the stability compared to the single organic clathrate hydrates. Moreover, the mixed clathrate hydrate also has a much higher stability compared to a pure hydrogen structure II clathrate hydrate. Therefore, the organic compounds act as promoter materials. The stabilities of the single and mixed organic clathrate hydrates with hydrogen showed the following trend in increasing order: 1,3-dioxolane {\textless} 2,5-dihydrofuran {\textless} tetrahydropyran {\textless} furan {\textless} cyclopentane, indicating that both size and geometry of the organic compound determine the stability of the clathrate hydrates. © 2011 Elsevier B.V.

In situ ATR-IR spectroscopy was used to simultaneously measure the sorption and swelling of carbon dioxide at high pressures in a biocompatible acrylate copolymer poly(methylmethacrylate-co-ethylhexylacrylate-co- ethyleneglycoldimethacrylate), P(MMA-EHA-EGDMA). The $ν$ 3 band of CO 2 dissolved in the polymer (at 2335 cm -1 ) was used to calculate the sorption data and the polymer swelling was determined by analyzing the changes in the absorbance of the $ν$(CO) band (at 1730 cm -1 ) of the polymer. Transmission spectroscopy in the near-IR region was also used to study the sorption of CO 2 in the polymer using combinational and overtone bands. The experiments were carried out in a pressure range of 2.0-12.0 MPa and in a temperature range of 27-40 °C. The data for CO 2 sorption in this polymer obtained by in situ spectroscopic methods have been compared to the data obtained by the gravimetric technique. © 2005 Elsevier B.V. All rights reserved.