Investigation of functionalized carbon nanotubes' performance on carbon dioxide hydrate formation

被引:55
作者
Nashed, Omar [1 ,2 ]
Partoon, Behzad [1 ]
Lal, Bhajan [1 ,2 ]
Sabil, Khalik M. [3 ]
Shariff, Azmi Mohd [1 ,2 ]
机构
[1] Univ Teknol PETRONAS, Chem Engn Dept, Bandar Seri Iskandar 32610, Perak, Malaysia
[2] Univ Teknol PETRONAS, Res Ctr CO2, Tronoh 31750, Perak, Malaysia
[3] Heriot Watt Univ Malaysia, Sch Energy Geosci Infrastruct & Soc, Inst Petr Engn, 1 Jalan Venna P5-2, Putrajuya 62200, Malaysia
关键词
Gas hydrates; Kinetic hydrate promoters; Multi-wall carbon nanotubes; Enhancement ratio; Induction time; Functionalized carbon nanotubes; GAS HYDRATE; GRAPHITE NANOPARTICLES; CO2; DISSOCIATION; INHIBITION; STABILITY; KINETICS; RECOVERY; BROMIDE; WATER;
D O I
10.1016/j.energy.2019.02.193
中图分类号
O414.1 [热力学];
学科分类号
摘要
In this work, the impact of functional group on the thermodynamics and kinetics of CO2 hydrates are investigated experimentally. The hydroxylated multi-wall carbon nanotubes (OH-MWCNT) and carboxylated carbon nanotubes (COOH-MWCNT) along with pristine carbon nanotubes (MWCNT) are selected for this study. The carbon nanotubes are suspended in a 0.03 wt% sodium dodecyl sulfate (SDS) aqueous solution and the results are compared with SDS aqueous solution at the same concentration of 0.03 wt% and deionized water. The CO2 hydrate phase boundary and kinetic parameters of CO2 hydrate formation including induction time, the initial rate and amount of gas consumed, gas uptake, storage capacity, and water to hydrates conversion are studied. The results show that the nanofluids studied do not affect the equilibrium conditions of CO2 hydrates. In addition, 0.01 and 0.05 wt% of COOH-MWCNT mixed with 0.03 wt% SDS showed highest initial hydrate formation rate and gas uptake. Furthermore, a comparison between SDS and COOH-MWCNT (without stabilizer SDS) at 0.03 wt% revealed that addition of COOH-MWCNT to the water enhance the initial hydrates formation rate compared to SDS. (C) 2019 Elsevier Ltd. All rights reserved.
引用
收藏
页码:602 / 610
页数:9
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