Laboratory tests have been performed using a stirred cell where SI and SII gas hydrates have been formed under the presence of the kinetic inhibitor Poly Vinyl Caprolactam (PVCap) and INHIBEX. The latter is a mixture containing 50wt% PVCap 2k and 50wt% butyl glycol. The effect of PVCap is enhanced by the presence of butyl glycol; the latter acts as a synergist for the former. Dissociation temperatures were obtained and compared for hydrates formed 1) in presence of PVCap and 2) in presence of INHIBEX. The effect of INHIBEX concentration on the temperature of dissociation was also investigated. Systems containing INHIBEX dissociated at lower temperatures than the corresponding systems with only PVCap present. Furthermore, 3000 ppm INHIBEX mixtures were found to have higher dissociation temperatures than 1500 ppm INHIBEX mixtures.

Inhibitor containing systems were investigated for hydrate structures I and II. The kinetic inhibitor PVCap was added to the water phase for each hydrate structure. Dissociation temperatures were determined for various formation temperatures and PVCap concentrations. Obtained dissociation temperatures were compared with corresponding values calculated with CSMHYD. Differences between experimental and calculated values were compared for various formation temperatures and inhibitor concentrations. Comparison revealed that these parameters (formation temperature and concentration) had an effect on the dissociation temperature. Dissociation temperatures for hydrates formed at low degrees of subcooling were higher than for hydrates formed at large subcooling. The effect depended on the system pressure; apparently decreasing or vanishing with increasing pressure. Furthermore, the temperature of dissociation increased with the inhibitor dose.

The kinetic inhibitor Poly Vinyl Caprolactam (PVCap) was added as a kinetic inhibitor to the gas-water system. Different hydrate formers were used in order to obtain formation of the different hydrate structures (sI, sII and sH). All hydrate structures were formed with PVCap. The effect of applying different melting rates was investigated. The isochoric technique was used to obtain dissociation temperatures and corresponding pressures. The melting rate was found to be a parameter influencial for the dissociation temperature. Even for very slow melting rates such as 0.0125 Kelvin per hour, the final dissociation temperature was significantly higher that the dissociation temperature for the corresponding non-inhibited system.