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Stimulation of high temperature carbonate gas reservoirs using seawater and chelating agents: Reaction kinetics

机译:使用海水和螯合剂刺激高温碳酸盐气体储层:反应动力学

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The use of hydrochloric acid (HCl) in gas well stimulation of high temperature reservoirs is currently facing different challenges. These challenges include rapid corrosion of the well tubulars, face dissolution, very high and uncontrolled reaction rate, and formation damage in high clay content and iron-rich reservoirs. In this study, water-soluble diethylene triamine penta acetic acid (DTPA) chelating agent is introduced as alternative to eliminate the risk associated with HCl at high temperatures. In addition, the potential of using seawater to replace fresh water in the stimulation process is explored to save the cost of fresh water transportation to deep offshore oil and gas wells. The effect of seawater on the reaction kinetics of DTPA with carbonate rocks under high pressure and high temperature conditions is investigated using the rotating disk apparatus. The reactions of DTPA solution diluted with fresh water (DTPA/DI) and seawater (DTPA/SW) with carbonate rocks were carried out at the same conditions. In the case of fresh water, the reaction is controlled by the surface reaction regime. Adding HCl to adjust DTPA pH did not turn the reaction into a mass transfer controlled reaction like the case of using HCl alone. The heavy matrix of seawater increased the resistance of ions diffusion, which resulted in a low reaction rate and transformed the reaction into a mass transfer limited regime. Corrosion tests were carried out on production and coiled tubing coupons obtained from the gas wells and the results of the new DTPA/SW formulation is compared to the standard HCl formulation. DTPA showed very low corrosion rate of 0.0034 g/cm(2) without adding corrosion inhibitors compared to 0.205 g/cm(2) of 15 wt% HCl with 3% corrosion inhibitors while the industry limit is 0.0244 g/cm(2) in 6 h. The reaction regime of DTPA chelating agent with calcite is identified to be mass transfer limited in seawater and surface reaction limited in fresh water. The rate expression for the dissolution of Ca2+ in DTPA/SW solution is obtained. Coreflooding experiments were performed to determine the optimum injection rate using low permeability Indiana limestone core samples. The optimum injection rate required to stimulate a very deep carbonate gas well was found to be 1.4 bbl/min after scaling up the coreflooding results to field scale. The application of the new DTPA/SW formulation in treating deep gas wells is expected to save the cost of fresh water and eliminate the cost of corrosion inhibitors. (C) 2017 Elsevier B.V. All rights reserved.
机译:使用盐酸(HCl)在高温储层的气井刺激中目前面临不同的挑战。这些挑战包括井管的快速腐蚀,面部溶解,非常高,不受控制的反应速率,以及高粘土含量和富含铁储层的形成损伤。在该研究中,引入水溶性二亚乙基三胺五乙酸(DTPA)螯合剂作为在高温下消除与HCl相关的风险。此外,探讨了使用海水取代刺激过程中淡水的潜力,以节省新的陆上石油和天然气井的淡水运输成本。使用旋转盘装置研究了在高压和高温条件下用碳酸盐岩的DTPA反应动力学对DTPA反应动力学的影响。在相同条件下进行用淡水(DTPA / DI)和碳酸盐岩(DTPA / DI)和海水(DTPA / SW)稀释的DTPA溶液的反应。在淡水的情况下,反应由表面反应状态控制。加入HCl以调节DTPA pH没有将反应变成单独使用HCl的壳体的传质控制反应。海水重基质增加了离子扩散的抗性,从而导致反应速率低,并将反应转化为质量转移限制。在从气井获得的生产和盘绕管道优惠券上进行腐蚀试验,并将新DTPA / SW配方的结果与标准的HCl制剂进行比较。 DTPA显示出非常低的腐蚀速率0.0034g / cm(2),而无需加入腐蚀抑制剂,而在0.205g / cm(2)的15wt%HCl中,具有3%的腐蚀抑制剂,而行业限为0.0244g / cm(2) 6小时。 DTPA螯合剂与方解石的反应条件被鉴定为在淡水中的海水和表面反应中的质量转移限制。获得DTPA / SW溶液中Ca2 +溶解的速率表达。进行CoreFlood实验以确定使用低渗透性印第安纳植物核心核心样品的最佳注射率。在将Core-odering结果缩放到现场规模之后,发现刺激非常深碳酸盐气井所需的最佳注射率为1.4 bbl / min。预计新的DTPA / SW配方在处理深气井中的应用将节省淡水的成本,消除腐蚀抑制剂的成本。 (c)2017 Elsevier B.v.保留所有权利。

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