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Impact of Organic Acids/Chelating Agents on the Rheological Properties of an Amidoamine Oxide Surfactant

机译:有机酸/螯合剂对酰胺胺氧化物表面活性剂的流变性质的影响

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Surfactant-based acids have been used for acid diversion because they are less damaging to the formation. Amphoteric viscoelastic surfactant is the main type of surfactants being used today. Low viscosity is observed in the live acid systems, whereas significantly increased viscosity is found when HC1 reacts with carbonate and generates divalent salts. The surfactant-acid system can be broken after acid treatments by mixing with reservoir hydrocarbons, or by using an external or internal breaker. Amidoamine oxide, an amphoteric surfactant, was examined in this work. The prepared surfactant-based live acid system contained 20 wt% HC1, 4 wt% surfactant and 1 wt% corrosion inhibitor. Different organic acids/chelating agents were added to live and spent acids. Calcium carbonate particles were used to neutralize live acids. The objective was to examine how these organic acids/chelating agents affected the rheological properties of spent acid systems. Measurements were made at temperatures from 75 to 200 °F, at a shear rate of 10 s~(-1) at 300 psi. Several simple organic acids (formic acid, acetic acid, propionic acid, and butyric acid), chelating agents (glycolic acid, lactic acid, gluconic acid, citric acid, tetrasodium EDTA, tetrasodium GLDA and disodium HEIDA) that are used in the field were examined. Experimental results indicated that the addition of organic acid/chelating agents significantly reduced the viscosity of spent acids. This reduction in viscosity increased with the number of carbon atoms in the acid. The addition of organic acids reduced the temperature range where the surfactant can be used. Chelating agents (a-hydroxyl carboxylic acids and amino acids) also tended to break the surfactant gel if enough acid was used. Based on the results obtained, organic acids can be used to break surfactant gel. TEM tests were first conducted to examine how organic acids/chelating agents interfered with the formation of rod-like micelles in the surfactant-based acid. The results showed that the addition of organic acids to the spent acid generated less elongated micelle structures and resulted in less apparent viscosity. In addition, if chelating agents or simple organic acids are used, then the concentration of the surfactant should be increased to compensate for the loss of viscosity induced by the addition of the organic acids.
机译:基于表面活性剂的酸已被用于酸性转移,因为它们对形成的损害较小。两性粘弹性表面活性剂是今天使用的主要类表面活性剂。在活性酸系统中观察到低粘度,而当HC1与碳酸酯反应并产生二价盐时,发现粘度显着增加。通过用储液烃混合或使用外部或内断路器,可以在酸处理后破裂表面活性剂 - 酸系统。在这项工作中检查了酰胺胺氧化物,两性表面活性剂。所制备的基于表面活性剂的活酸系统含有20wt%HCl,4wt%表面活性剂和1wt%腐蚀抑制剂。加入不同的有机酸/螯合剂以活化和废酸。碳酸钙颗粒用于中和活酸。目的是检查这些有机酸/螯合剂如何影响废酸系统的流变性质。在75至200°F的温度下测量,以300psi的剪切速率为10 s〜(-1)。几种简单的有机酸(甲酸,乙酸,丙酸和丁酸),螯合剂(乙醇酸,乳酸,葡萄糖酸,柠檬酸,四钠EDTA,四钠,四沸石,四沸石和赫达钠)是检查。实验结果表明,添加有机酸/螯合剂的添加显着降低了废酸的粘度。这种粘度的降低随酸中的碳原子的数量增加。加入有机酸降低了可以使用表面活性剂的温度范围。如果使用足够的酸,螯合剂(α-羟基羧酸和氨基酸)也倾向于破坏表面活性剂凝胶。基于所得的结果,有机酸可用于破坏表面活性剂凝胶。首先进行TEM测试以检查有机酸/螯合剂如何干扰表面活性剂基酸中的胶质胶束的形成。结果表明,将有机酸加入到废酸产生的较少细长的胶束结构上,并导致表观较小的粘度。另外,如果使用螯合剂或简单的有机酸,则应增加表面活性剂的浓度以补偿通过加入有机酸诱导的粘度的损失。

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