Porous hydrogel microspheres were synthesised and mixed with dry-water forming a colloidal system-Formation of methane gas hydrates in the colloidal system was fast and high in hydration capacity-The system is reusable for methane storage Highlights.docx
Six novel polymer-based kinetic hydrate inhibitors (KHIs)
were synthesized and characterized. Their performance in inhibiting
both tetrahydrofuran (THF) hydrate and the synthetic gas hydrate formation
was examined using two different instruments: a ball-stop apparatus
and a high-pressure automatic lag time apparatus (HP-ALTA). Performance
was benchmarked against two commercially available KHIs, Gaffix VC-713
and Luvicap EG, under the same working conditions. The test results
from the ball-stop rig demonstrated that the new KHIs were as effective
as Gaffix VC-713 and Luvicap EG in preventing the formation of THF
hydrates in 3.5 wt % NaCl solutions. For the synthetic gases, most
new polymers outperformed the reference KHIs at a concentration of
0.05 wt %. Polymers containing a pendant THF functional group in the
side chains showed a substantial 12–16 °C decrease in
the hydrate formation temperature of the gas water mixtures relative
to those containing the same amount of Gaffix VC-713 or Luvicap EG.
The trend of the inhibition performance of the polymers was different
in THF from that measured for gas mixtures. Small amounts of ethanol
added to the hydrate formation mixtures were also shown to have an
effect. Investigation of the inhibition mechanism associated with
these new polymers is under way.
In principle, one might prepare thin polymer membranes in an easy and economic way by generating a wetting layer of a polymerizable oil on a water surface, solidifying it, and transferring it to a solid substrate. However, there is hardly any oil that wets a water surface. One efficient way to assist the wetting of the water surface by an oil is to mix the oil with suitable particles. Theoretically, one expects several scenarios, which depend on the contact angles of the particles with the liquid interfaces. On the basis of these calculations, one can draw phase diagrams of particle-assisted wetting. In the current paper, we verify such a phase diagram of particle-assisted wetting experimentally.
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