An understanding of the mechanism for hydrate formation from water-in-oil emulsions is integral for progressing from preventing hydrate formation through expensive thermodynamic means to hydrate blockage prevention. This work presents hydrate formation and agglomeration in a stirred system studied using two complementary particle size analysis techniques, a Particle Video Microscope (PVM) and a Focused Beam Reflectance Measurement (FBRM). The PVM provides qualitative visual information through digital images in the black oil illuminated by a series of lasers. The FBRM provides a quantitative chord length distribution of the particles/droplets in the system. Three sets of experiments were performed using two different Crude oils, Conroe with a very small asphaltene content and poor emulsion stability, and Caratinga with a much higher asphaltene content and emulsion stability. The first experiments looked at ice as an analogy to hydrates, studying the morphology with both the PVM and FBRM. The second experiments looked at the effect of droplet size on hydrate formation and agglomeration, and the third set of experiments studied the dissociation process using a combination of the PVM and in situ conductivity measurements to determine the continuous phase. For hydrate formation, droplet size was found to have a major effect on whether or not agglomeration will occur. During dissociation agglomeration is extremely dramatic due to the creation of surface water on the particles. The dissociation of these agglomerates results in a significant destabilization of the suspension into a water/hydrate phase at the bottom of the cell until dissociation is complete. The dissociation conceptual picture presented illustrates an important implication when operating a flow line with hydrates present; dissociation within the pipeline should be prevented until the hydrates are out of the flow line.

An understanding of the blockage potential for an oil dominated system is an important step in moving from hydrate prevention to hydrate management. To better understand this problem a series of experiments were performed by varying the water cut, fluid velocity, and gas-liquid volume fraction using the ExxonMobil (XoM) flow loop in Houston, Texas, USA. The XoM large loop is a three pass, four inch internal diameter flow loop with a sliding vane pump capable of generating liquid velocities of up to 4 m/s. The systems that were studied include a range of water cuts from 5%-50% in a light crude oil (Conroe crude) and a gas phase of either pure methane for sI or 75% methane and 25% ethane which has sII as the thermodynamically stable phase. The results are compared with the hydrate plug prediction tool, CSMHyK, integrated into the multiphase flow simulator OLGA5®. The comparison between the model and the flow loop results serve as a basis for improving hydrate formation and plug prediction. In addition, the experimental variables that promote plug formation in the flow loop and how these may translate into the field are discussed.

Dissociation of gas hydrates has been the primary concern of the oil and gas industry for flow assurance, mainly in an offshore environment. There is also a growing interest in the rapid formation of gas hydrates for gas storage, transport of natural gas and carbon sequestration. In this thesis, we experimentally measure the kinetics of formation and dissociation of methane hydrates and the effect of various anionic and cationic surfactants such as sodium dodecyl sulfate (SDS), cetyl trimethylammonium bromide (CTAB) and alpha olefin sulfonate (AOS) on the association/dissociation rate constants. The importance and necessity of micelle formation in these surfactants has been studied. The effect of foam generation on the rate of formation of these hydrates has also been measured. SDS was found to significantly decrease the induction time for hydrate formation. There was an added decrease in the induction time when a foamed mixture of water and SDS was used. On the other hand CTAB and AOS had an inhibiting effect. The contribution of micelles towards promoting hydrate formation was demonstrated with a series of experiments using SDS. The micelles formed by these surfactants appear to serve as nucleation sites for the association of hydrates. New experimental data is presented to show that some surfactants and the use of foam can significantly increase the rate of hydrate formation. Other surfactants are shown to act as inhibitors. A new experimental setup is presented that allows us to distinguish between surfactants that act as promoters and inhibitors for hydrate formation. / text

Studying clathrate hydrates is, ideally, a simple task: one just have to keep water under a gas pressure. However, when trying to collect measurements in an accurate and repeatable way, things mess up. When, in particular, kinetic characterizations are required, not only pressure and temperature have to be measured: also particular parameters such as gas evolved/trapped during time, heat released/adsorbed during time, critical phenomena related to additive addition, etc, should be collected in a finer way. In the last years a growing interest has been devoted to investigations on the effects of a wide range of compounds capable to affect the thermodynamics and, in particular, kinetics of clathrate hydrate formation. The study of the effects of these compounds, called conditioners, requires an improvement of the performances of usual lab facilities by introducing a new strategy for the measurement of further characterizing parameters. Presently no standardization of the apparatus designed for clathrate hydrate studies exists, nor any commercial instrumentations are available. Generally, apparatus used are custom-made by the same research team according with the peculiar research requirements To do this we have designed, built, calibrated and tested a novel apparatus that, in addition to the ability of measuring usually unexplored parameters, is based on the idea of obtaining as many parameters as possible in a single formation batch. This in order to solve the problem of collecting a dataset that can be processed homogeneously, thus minimizing errors due stochastic behaviours. Using such an apparatus, several kinds of measurement are presented here, which are related directly to the clathrate hydrate investigation fields, but also more generally related to the study of equilibrium phases involving gaseous components.