Abstract
Natural gas hydrate plugging is one of the costly and challenging problems for the oil and gas industry, especially for subsea fields. One way to prevent gas hydrate formation at low cost is the use of low-dosage hydrate inhibitors (LDHI). Poly(N-isopropylmethacrylamide) (PNIPAM) with amide group have previously been shown to be an outstanding low-dosage hydrate inhibitor (LDHI). PNIPAMs are usually polymerized via radical polymerization, which can allow control over the molecular weight. We have synthesized PNIPAMs using control radical polymerization giving a fairly high degree of polymerization control. Additionally various Kinetic Hydrate Inhibitors (KHIs) were tested as CH4 hydrate inhibitors with polymeric hydrate inhibitor, PNIPAM. Furthermore, to check the synergetic effects of tetra butyl phosphonium bromide (TBPB), PNIPAM and their mixture TBPB-PNIPAM were tested as KHIs for methane gas hydrate formation. In this paper we present results on the performance of various polymeric inhibitors in KHI tests on methane gas in stirred autoclaves and on structure I hydrate formation. When PNIPAM alone was used as a single KHI, PNIPAM exhibited worst performance among the KHIs tested in this study. However the mixing of TBPB with PNIPAM further extended the induction time and reduced the CH4 hydrate growth rate. TBPB was an excellent synergist in blends with PNIPAM for kinetic hydrate inhibition of structure I forming CH4 hydrate. In summary, the mixture TBPB-PNIPAM was proven that great synergist for prevent the CH4 hydrate and good potential in achieving the industrial application of Oil & Gas production technology and therefore was a significantly meaningful discovery in the field of energy production.
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