期刊文献+

磺酸型表面活性剂清洁压裂液的性能研究 被引量:8

The Performance of Sulfonic Surfactant Clean Fracturing Fluid
下载PDF
导出
摘要 为研制新型清洁压裂液,采用脂肪酸甲酯磺酸钠与芥酸酰胺丙基甜菜碱复配得到了一种增稠剂MC-1,研究了MC-1及无机盐加量对压裂液黏度的影响,考察了压裂液(3%MC-1+5%KCl)的耐温性、耐剪切性、悬砂性和破胶性能。结果表明,MC-1与多种无机盐KCl、NH4Cl和Na Cl均有较好的协同性,其中与KCl的协同性最好,压裂液黏度随MC-1和KCl加量增大而增加;该压裂液具有较好的耐温耐剪切性和悬砂性,在80℃、砂比40%的条件下,砂子的沉降速度为1.18 mm/s;与煤油混合后在80℃下2 h内完全破胶,破胶液黏度为4.5 m Pa·s,表面张力为24 m N/m,界面张力为0.8764 m N/m。该压裂液可适用于小于90℃的地层使用。 For the development of a new clean fracturing fluid, a thickener MC-1 was obtained by compounding sodium fatty acid methyl ester sulfonate (MES) and erucyl amidopropyl carboxyl betaine (CAB). The effect of the content of MC-I and inorganic salt on the viscosity of MES fracturing fluid was studied. The temperature and shearing resistance, sand-carrying capacity and gel breaking performances of the clean fracturing fluid (3% MC-1 +4% KCl) were evaluated. The results showed that MC-1 thickener had a good compatibility with ionic salt, such as KCl,NH4Cl and NaCl, among which KCl was the best. The viscosity of fracturing fluid increased with increasing content of MC-1 and KCl. The fracturing fluid possessed good temperature tolerance and shearing resistance. The settling velocity was 1.18 mm/s on the condition of 80℃ and 40% sand ratio, which indicated that the fracturing fluid had a good sand-carrying capacity. The fracturing fluid completely broke down in 2 hrs at 80℃ with the addition of kerosene. The viscosity of the gel breaking liquid was 4.5 mPa. s, and the surface tension and interfacial tension of that was 24 mN/m and 0.8764 mN/m,respectively. The fracturing fluid was adapt to the formation whose temperature was smaller than 90℃.
出处 《油田化学》 CAS CSCD 北大核心 2016年第1期25-28,共4页 Oilfield Chemistry
基金 陕西省科技厅项目"陆相页岩气资源地质研究与勘探开发关键技术攻关/陆相页岩气储层压裂改造工艺技术攻关"(项目编号2012KTZB03) "高固含量聚氨酯-聚丙烯酸酯(PUA)微乳液的制备及其在水性涂料中的应用"(项目编号2014K08-11) "磺酸基高固含量聚氨酯-聚丙烯酸酯微乳液的微观结构及黏结固化机理"(项目编号2014JQ6221)
关键词 脂肪酸甲酯磺酸钠 芥酸酰胺丙基甜菜碱 清洁压裂液 fatty acid methyl ester sulfonate erucyl amidopropyl carboxyl betaine clean fracturing fluid
  • 相关文献

参考文献12

二级参考文献111

共引文献181

同被引文献70

引证文献8

二级引证文献36

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部