Natural Gas Hydrate Equilibria in Brine Including the Effect of Inhibitors on Hydrate Formation

Farzan Sahari Moghaddam, M. Mahmoodi, M. Zare, F. Goodarzi, M. Abdi, L. James
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引用次数: 1

Abstract

Preventing hydrate formation is critical to safely and economically manage subsea tiebacks. Thermodynamic Hydrate Inhibitors (THI) and Low Dosage Hydrate Inhibitors (LDHI) help manage hydrate formation. Here, we use a novel isothermal approach using a PVT cell to experimentally find the hydrate equilibrium point of natural gas and brine. In addition, a constant temperature and pressure condition is used to compare hydrate formation with and without hydrate inhibitors. First, to better understand the novel isothermal technique, natural gas-brine equilibrium experiments were conducted. Secondly, a constant pressure and temperature approach is used to investigate Kinetic Hydrate Inhibitors (KHIs) and low dosage methanol performance on hydrate formation. The formation and dissociation points are detected through a sudden drop or peak in the pressure profile, respectively, and by visual observation. To evaluate inhibitor performance, the experiments were conducted at challenging temperatures between -0.5°C to 3°C, applicable to the environment offshore Newfoundland and Labrador. Two commercial KHIs and one THI were tested. Both KHIs showed good performance up to certain level of subcooling according to their concentration. However, KHI-B performed better at inhibiting hydrates compared to KHI-A despite its lower concentrations compared to KHI-A. The induction time for 1 wt% KHI-A under 10°C subcooling at a temperature of 0.75°C was 311 min. The induction time for 1 wt% KHI-B under 12°C subcooling at a temperature of 2.66°C was 184 min. Yet, in the case of KHI B, with half the concentration (0.5 wt%), no hydrate formed at temperature of 1.21°C and 10°C subcooling. Low dosage methanol (a common THI) was also assessed. Although the induction time under 10.36°C subcooling and constant temperature of −0.43°C was only 47 min, no hydrate formed within 22 hours at −0.12°C under 7.5°C subcooling. This work uses a novel experimental isothermal approach by PVT cell to investigate hydrate equilibrium and the effectiveness of different inhibitors. Hence, a better understanding of natural gas hydrate equilibrium in brine is developed. Based on significant costs associated with injecting high quantities of THI (e.g., methanol) to prevent hydrate formation, this work also compares the performance of KHIs and low dosage THI (methanol).
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卤水中天然气水合物平衡及抑制剂对水合物形成的影响
防止水合物形成对于安全、经济地管理海底回接至关重要。热力学水合物抑制剂(THI)和低剂量水合物抑制剂(LDHI)有助于控制水合物的形成。本文采用一种新颖的等温方法,利用PVT池实验寻找天然气和盐水的水合物平衡点。此外,在恒温常压条件下,比较了有水合物抑制剂和没有水合物抑制剂的水合物形成情况。首先,为了更好地理解新的等温技术,进行了天然气-盐水平衡实验。其次,采用恒压恒温方法研究了动力学水合物抑制剂(KHIs)和低剂量甲醇对水合物形成的影响。形成点和解离点分别通过压力剖面的突然下降或峰值和目视观察来检测。为了评估抑制剂的性能,实验在-0.5°C至3°C之间的挑战性温度下进行,适用于纽芬兰和拉布拉多海上环境。测试了两架商用khe和一架THI。两种khe在一定过冷程度下均表现出良好的性能。然而,与KHI-A相比,KHI-B在抑制水合物方面表现更好,尽管其浓度低于KHI-A。1 wt% kh - a在10°C过冷条件下,在0.75°C过冷条件下的诱导时间为311 min。1 wt% kh -B在12°C过冷条件下,在2.66°C过冷条件下的诱导时间为184 min。然而,对于KHI B,当浓度为0.5 wt%时,在1.21°C和10°C过冷条件下没有形成水合物。低剂量甲醇(一种常见的THI)也进行了评估。虽然在10.36℃过冷和- 0.43℃恒温条件下的诱导时间仅为47 min,但在- 0.12℃过冷条件下,在7.5℃过冷条件下的22 h内未形成水合物。本研究采用一种新颖的PVT细胞等温实验方法来研究水合物平衡和不同抑制剂的有效性。从而对卤水中天然气水合物平衡有了更好的认识。考虑到注入大量THI(如甲醇)以防止水合物形成的巨大成本,本研究还比较了KHIs和低剂量THI(甲醇)的性能。
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