Comparative Analysis of Aminopolycarboxylate Chelants Improves Iron Control in Acidizing Operations

Ahmed H. El-Kady, Zheng-Qi Chai, Hisham A. Nasr-El-Din
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Abstract

Aminopolycarboxylate-based chelants are used to control iron precipitation during acidizing operations by interacting directly with the iron, resulting in water-soluble complexes. This paper highlights that, in order to improve the effectiveness of iron control during acidizing operations, the type and the concentration of the chelants should be based on the formation properties and the well characteristics by comparing the cheltors’ performance as iron-control agents at different temperatures and pH environments with different levels of iron concentrations and chelant to iron molar ratios in acid (HCl). This study also addresses the interactions between the tested iron-control additives and acid, as well as the performance of the chelants in carbonate cores. Laboratory experiments were conducted to investigate the performance of nitrilotriacetic acid (NTA), glutamic acid, N, N-diacetic acid (GLDA), diethylenetriaminepentaacetic acid (DTPA), ethylenediamine-tetraacetic acid (EDTA), and hydroxyethylethylenediaminetriacetic acid (HEDTA) as iron control additives in 5 wt% HCl at pH values 0 to 4.5 to simulate carbonate acidizing at temperatures of 70 to 300°F, and initial iron concentrations of 2000 ppm. The performance of NTA and EDTA was also compared at higher initial iron concentration (4000 ppm). This work also quantified the effects of acid additives such as corrosion inhibitor and non-ionic surfactant on the chelation performance. Coreflood experiments using carbonate cores in acid with chelant helped determine its influence on permeability. Testing chelant-to-acid molar ratios of 1:1, 1.1:1, 1.2:1, 1.3:1, 1.4:1, 1.5:1, and 2:1 relative to iron concentration yielded optimal values. Additional tests monitored iron precipitation in solution using an inductively coupled argon plasma (ICAP) emission spectroscopy. Precipitates were filtered and analyzed using X-ray diffraction (XRD), X-ray fluorescence (XRF), and scanning electron microscopy-energy dispersive spectroscopy (SEM-EDS). Without chelant, at 70°F and 2000 ppm initial iron concentration, precipitation began at pH 1.45 and completed by pH 2.42. At 150 and 210°F, iron precipitated at pH 0.68 and 0.3 and completed by pH 1.3 and 1, respectively. At 70°F, NTA showed a minimum of 98% chelation at pH 4.3; however, its performance declined at 150°F to 74% chelation at pH 4.24, and at 210°F to 53% chelation at pH 4.0. Although DTPA dissolves completely in live acid, precipitations occurred at partially spent acid. At pH 0.15, SEM-EDS showed that the precipitate contains as much as 13 wt% iron. Thus, DTPA is not a suitable iron-control agent. HEDTA showed a 90% chelation at 210°F and pH 4.8. GLDA's performance declined to less than 50% at 150°F. At higher iron concentrations of 4000 ppm, Na3NTA kept all iron in solution in a 5 wt% HCl up to pH 4.0 at 70°F and its performance declined to a minimum of 97% at pH 4.7 at same temperature. At 150°F, and 210°F, Na3NTA started to gradually decline at pH values greater than 3.9, and 3.5, respectively. The minimum chelation reached by NTA was 91% at pH 4.4, at 150°F, and 73% at pH 4 at 210°F. Upon comparing the NTA's results at high iron concentrations to the popular EDTA, Na4EDTA at 1-to-1 mole ratio with iron exceeded its maximum solubility in 5 wt% HCl and precipitated in the original solution. For NTA, a molar ratio of 1.4:1 is optimal at 70 and 150°F, showing chelation performance of 95% and 94%, respectively, while a molar ratio of 1.5:1 is optimal at 210°F, showing a chelation performance of 87%. This study's results improve field operations by identifying NTA and HEDTA as having the best iron-control chelation performance of the five additives tested, thus reducing guesswork and streamlining production. The work also provided recommendations for choosing the best type of iron-control agent based on solubility and coreflood analysis. The results can be used to design more efficient acidizing fluids. This work won second place in the Masters division of the 2020 Gulf Coast Regional Student Paper Contest, April 2020.
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氨基聚羧酸螯合剂的对比分析提高了酸化作业中的铁控制
氨基聚羧酸基螯合剂通过直接与铁相互作用,形成水溶性络合物,用于控制酸化操作过程中的铁沉淀。本文指出,为了提高酸化作业中的控铁效果,应根据地层性质和井的特点来选择螯合剂的类型和浓度,比较不同温度和pH环境、不同铁浓度水平和酸(HCl)中螯合剂与铁的摩尔比下螯合剂作为控铁剂的性能。本研究还研究了所测试的铁控制添加剂与酸之间的相互作用,以及碳酸盐岩心中螯合剂的性能。在实验室实验中,研究了硝酸三乙酸(NTA)、谷氨酸、N, N-二乙酸(GLDA)、二乙烯三胺五乙酸(DTPA)、乙二胺四乙酸(EDTA)和羟乙基二胺三乙酸(HEDTA)作为铁控制添加剂在5 wt% HCl条件下的性能,pH值为0 ~ 4.5,模拟了在70 ~ 300°F温度下、初始铁浓度为2000 ppm的碳酸盐酸化。在较高的初始铁浓度(4000ppm)下,比较了NTA和EDTA的性能。本工作还量化了酸性添加剂如缓蚀剂和非离子表面活性剂对螯合性能的影响。碳酸盐岩岩心在酸中加入螯合剂进行岩心驱替实验,确定了其对渗透率的影响。测试螯合剂与酸的摩尔比为1:1、1.1:1、1.2:1、1.3:1、1.4:1、1.5:1和2:1的铁浓度,得到最佳值。附加测试使用电感耦合氩等离子体(ICAP)发射光谱监测溶液中的铁析出。采用x射线衍射(XRD)、x射线荧光(XRF)和扫描电子显微镜-能谱(SEM-EDS)对析出物进行过滤和分析。在没有螯合剂的情况下,在70°F和2000 ppm初始铁浓度下,沉淀从pH 1.45开始,到pH 2.42完成。在150°F和210°F时,铁在pH为0.68和0.3时析出,在pH为1.3和1时完成。在70°F时,NTA在pH 4.3下显示至少98%的螯合;然而,在150°F时,pH值为4.24,螯合率为74%,在210°F时,pH值为4.0,螯合率为53%。虽然DTPA在活性酸中完全溶解,但在部分废酸中会发生沉淀。在pH为0.15时,SEM-EDS显示析出物含铁量高达13%。因此,DTPA不是一种合适的铁控制剂。在210°F和pH 4.8条件下,heta的螯合作用达到90%。在150°F时,GLDA的性能下降到50%以下。当铁浓度为4000 ppm时,Na3NTA在70°F下,在5 wt% HCl中保持所有铁直至pH 4.0,在相同温度下,当pH 4.7时,其性能下降到最低的97%。在150°F和210°F, Na3NTA开始逐渐下降,pH值分别大于3.9和3.5。在pH 4.4, 150°F时,NTA达到的最小螯合率为91%,在pH 4, 210°F时达到73%。将NTA在高铁浓度下的结果与常用的EDTA进行比较,Na4EDTA与铁的摩尔比为1时,超过了其在5 wt% HCl中的最大溶解度,并在原始溶液中沉淀。对于NTA,在70°F和150°F时,摩尔比为1.4:1最优,螯合性能分别为95%和94%,而在210°F时,摩尔比为1.5:1最优,螯合性能为87%。该研究的结果通过确定NTA和HEDTA在五种测试添加剂中具有最佳的铁控制螯合性能,从而减少了猜测并简化了生产,从而改善了现场操作。根据溶解度和岩心驱替分析,为选择最佳类型的铁控制剂提供了建议。研究结果可用于设计更高效的酸化液。该作品于2020年4月在2020年墨西哥湾沿岸地区学生论文竞赛的硕士赛区中获得第二名。
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