用螯合剂和转化器研究碳酸钙对重晶石溶解度的影响

K. Abdelgawad, M. Mahmoud, S. Elkatatny, S. Patil
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引用次数: 6

摘要

硫酸钡(Barite)是油气田生产设备内部和储层中常见的结垢之一。重晶石也是油气井钻井中常用的加重材料。在碳酸盐地层中也可能存在硫酸钡垢。碳酸钙地层中硫酸钡的脱除是一个具有挑战性的问题,因为碳酸钙在不同酸中的溶解度高于硫酸钡。此外,硫酸钡不溶于常规酸,如盐酸和其他有机酸。本文通过80℃下的溶解度实验,研究了碳酸钙对硫酸钡在螯合剂和转化器催化剂中的溶解度的影响。在pH值为12的条件下,使用20 wt.% DTPA和6 wt.%碳酸钾(转化器)。研究了钙螯合对硫酸钡溶解度的影响。第一种情况是硫酸钡首先溶解,然后溶液与碳酸钙反应。第二种情况是碳酸钙和硫酸钡同时暴露在DTPA溶液中。此外,碳酸钙负荷对硫酸钡溶解度的影响,分别用25%、50%、75%和100wt %的水垢作为碳酸钙进行了测定。采用电感耦合等离子体(ICP)作为评价标准,分析阳离子浓度,确定各垢型的溶解度。在硫酸钡溶解的两种情况下,碳酸钙的存在对硫酸钡的溶解度有显著影响。当DTPA溶液在24h后首先被钡离子饱和时,在溶液中加入碳酸钙,溶液中的钡会立即下降(在50ml溶液中,浓度在30min内从2140 ppm下降到1984 ppm),引起硫酸钡的沉淀。此外,碳酸钙和硫酸钡同时螯合时,硫酸钡的溶解度比碳酸钙低。这可以解释为DTPA对钙的亲和力比钡高。强烈建议在设计使用DTPA去除硫酸钡垢的化学配方时考虑到任何钙源的存在。因此,砂岩地层推荐使用DTPA处理配方。如果忽略碳酸盐岩中的Ca2+螯合作用,现场结果可能与实验室结果完全不同。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Effect of Calcium Carbonate on Barite Solubility Using a Chelating Agent and Converter
Barium Sulfate (Barite) is one of the common oil and gas field scales formed inside the production equipment and in the reservoir. Barite is also a common weighting material used during drilling oil and gas wells. Barium sulfate scale may exist as well in carbonate formations. The removal of barium sulfate from calcium carbonate formation is a challenging problem because of the solubility of calcium carbonate is higher compared to that of barium sulfate in different acids. In addition, barium sulfate is not soluble in the regular acids such as hydrochloric (HCl) acid and other organic acids. In this paper, the effect of calcium carbonate on barium sulfate solubility in a chelating agent and converter catalyst was investigated using solubility experiments at 80°C as a function of time. 20 wt.% DTPA with 6 wt.% potassium carbonate (converter) were used at pH of 12. The effect of calcium chelation on the barium sulfate solubility was studied in two scenarios. The first scenario when Barium sulfate is dissolved first then the solution reacts with calcium carbonate. The second scenario when both calcium carbonate and barium sulfate are exposed to the DTPA solution at the same time. In addition, the effect of calcium carbonate loading on the barium sulfate solubility was determined using 25, 50, 75, and 100 wt.% of the scale as calcium carbonate. As an evaluation criterion, inductively coupled plasma (ICP) was used to analyze the cation concentration and determine the solubility of each scale type. For the two scenarios of barium sulfate dissolution, the presence of calcium carbonate had a significant effect on the solubility of barium sulfate. When DTPA solution got saturated first with barium cations after 24 hours, and the addition of calcium carbonate to the solution will cause immediate barium drop of solution (concentration drop from 2140 to 1984 ppm in 30 min in 50 ml solution) which cause precipitation of barium sulfate. In addition, simultaneous chelation of both calcium carbonate and barium sulfate showed a low barium sulfate solubility compared to calcium carbonate. This can be explained by the high affinity of DTPA to calcium compared to barium. It is highly recommended to account for the presence of any calcium source during the design of the chemical formulation for barium sulfate scale removal using DTPA. Therefore, DTPA treatment formulation is recommended in sandstone formations. Field results can be completely different from laboratory results if Ca2+ chelation from carbonate rocks is ignored.
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