Affiliations 

  • 1 Department of Chemical Engineering, Faculty of Technical Engineering, Bright Star University, El-Brega 218645, Libya
  • 2 Department of Biological and Chemical Engineering, Aarhus University, Universitetsbyen 36, 8000 Aarhus, Denmark
  • 3 Chemical Engineering Department, Universiti Teknologi PETRONAS, Bandar Seri Iskandar 32610, Perak, Malaysia
  • 4 PETRONAS Research Sdn Bhd, Kawasan Institusi Bangi, Lot 3288 3289 Off Jalan Ayer Itam, Kajang 43000, Selangor, Malaysia
  • 5 U.S. Pakistan Centre for Advance Studies in Energy, Department of Thermal Energy Engineering, National University of Science and Technology, Islamabad 44000, Pakistan
Materials (Basel), 2022 Dec 05;15(23).
PMID: 36500166 DOI: 10.3390/ma15238670

Abstract

Hydrate-based technology has yet to find its way to commercial applications due to several issues, including formation conditions and slow kinetics. Several solid particles were introduced to speed up hydrate formation. However, these solid compounds have given contradictory results. This study investigated the effect of high thermal conductive metallic nanofluids of silver (Ag) and copper (Cu) on CH4 and CO2 hydrates. The solid particles were suspended in a 0.03 wt% SDS aqueous solution, and the results were compared with the 0.03 wt% SDS and deionized water samples. A stirred tank batch reactor was used to conduct the thermodynamic and kinetic experiments. The thermodynamic study revealed that 0.1 wt% of solid particles do not shift the equilibrium curve significantly. The kinetic evaluation, including induction time, the initial rate of gas consumption, half-completion time, t50 and semi-completion time, t95, gas uptake, and storage capacity, have been studied. The results show that the Ag and Cu promote CH4 hydrates while they inhibit or do not significantly influence the CO2 hydrates formation. A predictive correlation was introduced to get the apparent rate constant of hydrate formation in the presence of metal-based fluid at the concentrations range of 0.005-0.1 wt%.

* Title and MeSH Headings from MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.