引用本文:
【打印本页】   【HTML】   【下载PDF全文】   查看/发表评论  【EndNote】   【RefMan】   【BibTex】
←前一篇|后一篇→ 过刊浏览    高级检索
本文已被:浏览次   下载 本文二维码信息
码上扫一扫!
分享到: 微信 更多
磺甲基酚醛树脂高温交联影响因素及控制方法
孙明波1,张敬春2
(1.中国石油大学石油工程学院,山东青岛 266580;2.山东大学胶体与界面化学教育部重点实验室,山东济南 250100)
摘要:
考察磺甲基酚醛树脂高温交联的机制及影响因素,提出两种控制磺甲基酚醛树脂高温交联的方法。结果表明:体系的pH值越高,矿化度越大,反应温度越高、时间越长,磺甲基酚醛树脂交联越剧烈;磺甲基酚醛树脂分子间的交联反应主要是酚环上羟甲基(苄羟基)与活泼氢发生脱水缩合生成亚甲基桥的反应;氧化剂和磺化剂可以减少酚环上的羟甲基的数量,在聚磺钻井液中可以有效控制磺甲基酚醛树脂的高温交联,提高钻井液的高温稳定性。
关键词:  磺甲基酚醛树脂  交联  钻井液  羟甲基  固体核磁共振
DOI:10.3969/j.issn.1673-5005.2014.06.026
分类号::TQ 323.1
基金项目:
Influence factors and control methods of high-temperature crosslinking for sulphonated methyl phenolic resin
SUN Mingbo1, ZHANG Jingchun2
(1.School of Petroleum Enginnering in China University of Petroleum, Qingdao 266580, China;2.Key Laboratory for Colloid and Interface Chemistry of the Ministry of Education, Shandong University, Jinan 250100, China)
Abstract:
The crosslinking mechanism and the associated influence factors of sulphonated methyl phenolic resin(SMP) at high temperatures were investigated. And two control methods of high-temperature crosslinking for SMP were proposed. It is found that the crosslinking is promoted with higher pH value, bigger salinity, higher reaction temperature and longer time. The solid nuclear magnetic resonance (NMR) and infrared results indicate that the crosslinking is a dehydration condensation reaction between the hydroxymethyl and active hydrogen on the phenol ring, which forms methylene bridge. Hence, oxidant and sulfonating agent can be utilized to reduce the hydroxymethyl amount on the phenol ring. In this way, the crosslinking reaction of SMP at high temperature could be controlled, through which the stability of polysulfonate drilling fluid at high temperature is improved.
Key words:  sulphonated methyl phenolic resin  crosslinking  drilling fluids  hydroxymethyl  solid NMR
版权所有 中国石油大学学报(自然科学版)编辑部 Copyright©2008 All Rights Reserved
主管单位:中华人民共和国教育部 主办单位:中国石油大学(华东)
地址: 青岛市黄岛区长江西路66号中国石油大学期刊社 邮编:266580 电话:0532-86983553 E-mail: journal@upc.edu.cn
本系统由:北京勤云科技发展有限公司设计