CH4 purification and CO2 removal by hydrate-based separation method from the simulated
biogas (64 mol % CH4/CO2) were investigated
in tetrabutylammonium bromide (TBAB) solution. Three different hydrate
additives were combined with TBAB to study the synergistic influence
on thermodynamics and kinetics of hydrate formation. These additives
were 1-butyl-3-methylimidazolium hexafluorophosphate ([EMIM]BF4), sodium dodecyl benzene sulfonate (SDBS), and propylene
carbonate (PC). The thermodynamic experiment results showed that [EMIM]BF4 and PC have an inhibition effect on CO2 and CO2/CH4 hydrate formation. SDBS has a little influence
on phase equilibrium. As for the results of hydrate kinetic and biogas
hydrate separation, CH4 mole fraction in the remaining
gas could reach 79.20 mol % from the initial 64.0 mol %, and CH4 recovery was 94.21% in TBAB + [EMIM]BF4 solution
when the operation conditions were 3.5 MPa and 277.15 K. CO2 mole fraction in the hydrate phase could reach 50 mol % or even
higher from the initial 36.0 mol %. The gas storage in the hydrate
phase did not change dramatically. Basically, the gas storage in the
hydrate phase was 0.07 mol on account of addition of TBAB. The CO2 hydrate ratio was about 55%, and it did not change widely.
On the whole, the overall effect of biogas hydrate separation in TBAB
solution was [EMIM]BF4 > PC > SDBS.
CH 4 concentration and CO 2 separation from biogas (CH 4 /CO 2 ) by an one-stage hydrate formation was supposed to be a prospective and economical practicable technology compared with traditional gas separation methods. We investigated the influence of 1-butyl-3-methylimidazolium hexafluorophosphate ([BMIM] PF 6 ) on simulated biogas (64.0 mol %CH 4 /CO 2 ) hydrate separation in this work. The thermodynamic promoter TBAB was combined with [BMIM] PF 6 to investigate binary gas hydrate formation and separation efficiency. Different parameters which affected hydrate formation were investigated. The concentration of [BMIM] PF 6 was 1000/2000/3000 ppm, and the optimized concentration of TBAB was 4 wt %. With respect to the hydrate gas separation results, the addition of TBAB can decrease CH 4 /CO 2 hydrate formation pressure greatly and the hydrate formation induction time. CH 4 in the remaining gas can be increased from 64.0 to 79.90 mol %, and CH 4 recovery can arrive at 95.83%. Meanwhile, the addition of [BMIM] PF 6 could increase the CO 2 mole friction in hydrate from 36.0 to 58.63 mol %. So it was demonstrated that the combination of TBAB + [BMIM] PF 6 would have a great application prospect on biogas purification technology.
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