scholarly journals Inhibition Effect of Kinetic Hydrate Inhibitors on the Growth of Methane Hydrate in Gas–Liquid Phase Separation State

Energies ◽  
2019 ◽  
Vol 12 (23) ◽  
pp. 4482
Author(s):  
Liwei Cheng ◽  
Limin Wang ◽  
Zhi Li ◽  
Bei Liu ◽  
Guangjin Chen

The effect of kinetic hydrate inhibitors (KHIs) on the growth of methane hydrate in the gas–liquid phase separation state is studied at the molecular level. The simulation results show that the kinetic inhibitors, named PVP and PVP-A, show good inhibitory effects on the growth of methane hydrate under the gas–liquid phase separation state, and the initial position of the kinetic hydrate inhibitors has a major effect on the growth of methane hydrates. In addition, inhibitors at different locations exhibit different inhibition performances. When the inhibitor molecules are located at the gas–liquid phase interface, increasing the contact area between the groups of the inhibitor molecules and methane is beneficial to enhance the inhibitory performance of the inhibitors. When inhibitor molecules are located at the solid–liquid phase interface, the inhibitor molecules adsorbed on the surface of the hydrate nucleus and decreased the direct contact of hydrate nucleus with the surrounding water and methane molecules, which would delay the growth of hydrate nucleus. Moreover, the increase of hydrate surface curvature and the Gibbs–Thomson effect caused by inhibitors can also reduce the growth rate of methane hydrate.

1985 ◽  
Vol 40 (7) ◽  
pp. 693-698 ◽  
Author(s):  
M. Woznyj ◽  
H.-D. Lüdemann

The phase diagram t-butanol/water is studied in the temperature range between 200 and 450 K at pressures up to 200 MPa. No liquid/liquid phase separation is observed in this range. The solid/liquid phase diagram reveals the presence of a stable t-butanol/dihydrate at all pressures. At the t-butanol rich side of the diagram solid mixtures with compositions t-butanol/water ~ 5 :1 and ~ 6 : 1 are observed.


1997 ◽  
Vol 36 (4) ◽  
pp. 103-110 ◽  
Author(s):  
István Licskó

The processes leading from coagulant feed to the development of flocs suited to solid-liquid phase separation are examined and analyzed in the light of available information and experimental data. It is concluded that at the relatively high buffering capacity (HCO3− concentration above 1.8 meg/L) and close to neutral pH values (7.0<pH<8.4) typically found in the surface waters of Hungary, flocs suited to solid-liquid phase separation develop from the coagulant added within a very short period of time (10-20 seconds). These flocs are not capable of changing the charge of the particles on the colloidal, quasi-colloidal, or destabilizing the dispersion. Between the hydrolysis of the coagulant and the development of large flocs, “short-lived” water soluble aluminium and iron(III) hydroxide complexes, metal hydroxide sols are formed, which also carry a positive charge. These latter two metal hydroxide types (which also exist for a brief period - a few seconds - only) are the ones capable of destabilizing the dispersion. The bond between the suspended solids to be removed and the metal hydroxide sols and water soluble metal hydroxide complexes must be established within this short period. Rapid mixing of the coagulant will ensure rapid hydrolysis of the coagulant, contact between the sols and the suspended solids and will retard the development of large flocs which are inactive in destabilizing the dispersion.


2013 ◽  
Vol 48 (1) ◽  
pp. 664-673 ◽  
Author(s):  
D. K. Villa-Gomez ◽  
E. D. van Hullebusch ◽  
R. Maestro ◽  
F. Farges ◽  
S. Nikitenko ◽  
...  

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