Comparing the Kinetic Hydrate Inhibition Performance of Linear versus Branched Polymers.

Kinetic hydrate inhibitors (KHIs) are a chemical method of preventing gas hydrate plugging of oil and gas production flow lines. The main ingredient in a KHI formulation is one or more water-soluble amphiphilic polymers. Poly(N-vinyl caprolactam) (PVCap) is an unbranched polymer and a well-known industrial KHI, often used as a yardstick to compare the performance of new polymers. The effect of branching PVCap on KHI performance has been investigated by polymerizing the VCap monomer in the presence of varying amounts of trimethylolpropane triacrylate, pentaerythritol tetraacrylate, or bis-pentaerythritol hexaacrylate cross-linkers to give PVCap polymers with 3, 4, and 6 branches, respectively. If the ratio of cross-linker to VCap was too high (6:1 to 8:1), gelling and/or poor water solubility was observed, giving short polymer chains and poor KHI efficacy. For higher ratios (30:1 to 60:1), it was found that the concentration of the polymer needed to give total inhibition of structure II tetrahydrofuran hydrate crystal growth could be lowered by using tribranched rather than linear PVCap. Slow constant cooling (1 °C/h) gas hydrate experiments with a synthetic natural gas in steel rocking cells at 76 bar were also carried out. A small improvement in KHI performance was observed for one of the branched PVCaps compared with a linear PVCap. Branched and linear poly(N-isopropylmethacrylamide) (PNIPMAm) polymers were also investigated in the gas hydrate system, but there was no benefit observed when branching this polymer class.

Improved Gas Hydrate Kinetic Inhibition for 5-Methyl-3-vinyl-2-oxazolidinone Copolymers and Synergists.

Kinetic hydrate inhibitors (KHIs) are used to prevent deposits and plugging of oil and gas production flow lines by gas hydrates. The key ingredient in a KHI formulation is a water-soluble amphiphilic polymer. Recently, polymers of a new commercially available 5-ring vinylic monomer 5-methyl-3-vinyl-2-oxazolidinone (VMOX) were investigated as KHIs and shown to perform better than some commercial KHI polymers such as poly(N-vinyl pyrrolidone). This initial study using slow constant cooling (SCC) in rocking cells with a synthetic natural gas has now been expanded to further explore low molecular weight PVMOX homopolymers and VMOX copolymers as well as blends with nonpolymeric synergists. A PVMOX homopolymer with improved KHI performance was found using 3-mercaptoacetic acid as a chain transfer agent in the radical polymerization of VMOX. Among a range of copolymers, VMOX:n-butyl acrylate copolymers in particular gave good KHI performance, better than the PVMOX homopolymer. Among the potential synergists, trialkylamine oxides (alkyl = n-butyl or iso-pentyl) and tetra(n-pentyl)ammonium bromide to 2500 ppm were found to be antagonistic with PVMOX at the test concentrations while some alcohols and glycols were synergetic. The best synergist was 2,4,7,9-tetramethyl-5-decyne-4,7-diol (TMDD). For example, a mixture of 2500 ppm TMDD with 2500 ppm PVMOX (Mw 2400 g/mol) performed significantly better than 5000 ppm PVMOX. Addition of 1250 ppm TMDD to 2500 ppm VMOX:n-butyl acrylate 6:4 copolymer lowered the hydrate onset temperature in SCC tests by a further 3 °C compared to the copolymer alone giving hydrate onset at 4.2 °C.

Oxyvinylenelactam Polymers-A New Class of Lactam-Based Kinetic Hydrate Inhibitor Polymers.

The deployment of kinetic hydrate inhibitors (KHIs) is a chemical method for the prevention of gas hydrate plugging in gas, condensate, and oil production flow lines. Polymers made using the monomer N-vinylcaprolactam (VCap) are one of the most common KHI classes. Alternative classes of polymers containing caprolactam groups are rare. Here, we present a study on oxyvinylenelactam polymers and copolymers with pendant piperidone or caprolactam groups. Low-molecular-weight homo- and copolymers were obtained. The nonrotating vinylene groups impart rigidity to the polymer backbone. Poly(oxyvinylenecaprolactam) (POVCap) was insoluble in water, but poly(oxyvinylenepiperidone) (POVPip) and OVPip:OVCap copolymers with 60+ mol % OVPip were soluble with low cloud points. KHI screening tests were carried out using the slow constant cooling method in steel rocking cells. POVPip was water soluble with no cloud point up to 95 °C but showed a poor KHI performance. In contrast, OVPip:OVCap copolymers with about 60-70 mol % OVPip were also water soluble and showed a reasonable KHI performance, better than that of poly(N-vinylpyrrolidone) but not as good as that of poly(N-vinylcaprolactam). Surprisingly, several additives known to be good synergists for VCap-based polymers showed negligible synergy or were antagonistic with the 62:38 OVPip:OVCap copolymer with regard to lowering the onset temperature of hydrate formation. However, a blend with hexabutylguanidinium chloride showed a strong effect to delay the onset of rapid hydrate formation.