{"title":"纳米粒子增强聚合物凝胶的制备与耐温机理","authors":"Mingjia Liu, Jijiang Ge, Guicai Zhang, Meijie Wang, Dengya Chen, Ping Jiang, Haihua Pei, Weixiong Chen, Jiasu Li","doi":"10.1007/s00396-024-05253-y","DOIUrl":null,"url":null,"abstract":"<div><p>In order to solve the problem of poor stability of HPAM (partially hydrolyzed polyacrylamide) gel as a plugging agent at 150 °C, this paper investigates the preparation of a polymer gel strengthened with nano-SiO<sub>2</sub>, exhibiting good thermal stability, using a low-cost, low-hydrolysis anionic polymer. The experimental results indicated that when the gel was prepared with 1 wt% HPAM, 1 wt% water-soluble phenolic resin (WSPR) as a crosslinker, and 1 wt% nano-SiO<sub>2</sub> as a stabilizer, the dehydration rate of the gel was less than 5 wt% after 180 days of aging at 150 °C. In order to identify the stability mechanism of nano-SiO<sub>2</sub>-strengthened polymer gel, we conducted rheological tests, Cryo-SEM analysis, Fourier transform infrared (FTIR) spectroscopy, and solid-state nuclear magnetic resonance (NMR) analysis on the polymer gel before and after adding nanoparticles. The methods described in the study demonstrate the excellent long-term thermal stability of the polymer gel strengthened with nano-SiO<sub>2</sub> from both chemical bonding and microscopic perspectives. The results of rheological experiments indicated that the addition of nanoparticles improved the yield stress and long-term thermal stability of the gel. The scanning electron microscope (SEM) microstructure analysis confirmed that the addition of nanoparticles resulted in high-density cavities between the microscopic network structures of the gel. This facilitated the trapping of a significant amount of free water and the formation of a stable spatial mechanical support structure, ultimately enhancing the macro-mechanical strength of the gel. Additionally, FTIR and NMR experiments demonstrated that the nanoparticles effectively inhibited the hydrolysis of amide groups to carboxylate, thereby significantly preventing the high-temperature degradation of the gel and maintaining its strength after prolonged aging.</p><h3>Graphical abstract</h3>\n<div><figure><div><div><picture><source><img></source></picture></div></div></figure></div></div>","PeriodicalId":520,"journal":{"name":"Colloid and Polymer Science","volume":null,"pages":null},"PeriodicalIF":2.2000,"publicationDate":"2024-04-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Preparation and temperature resistance mechanism of nanoparticle-enhanced polymer gel\",\"authors\":\"Mingjia Liu, Jijiang Ge, Guicai Zhang, Meijie Wang, Dengya Chen, Ping Jiang, Haihua Pei, Weixiong Chen, Jiasu Li\",\"doi\":\"10.1007/s00396-024-05253-y\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><p>In order to solve the problem of poor stability of HPAM (partially hydrolyzed polyacrylamide) gel as a plugging agent at 150 °C, this paper investigates the preparation of a polymer gel strengthened with nano-SiO<sub>2</sub>, exhibiting good thermal stability, using a low-cost, low-hydrolysis anionic polymer. The experimental results indicated that when the gel was prepared with 1 wt% HPAM, 1 wt% water-soluble phenolic resin (WSPR) as a crosslinker, and 1 wt% nano-SiO<sub>2</sub> as a stabilizer, the dehydration rate of the gel was less than 5 wt% after 180 days of aging at 150 °C. In order to identify the stability mechanism of nano-SiO<sub>2</sub>-strengthened polymer gel, we conducted rheological tests, Cryo-SEM analysis, Fourier transform infrared (FTIR) spectroscopy, and solid-state nuclear magnetic resonance (NMR) analysis on the polymer gel before and after adding nanoparticles. The methods described in the study demonstrate the excellent long-term thermal stability of the polymer gel strengthened with nano-SiO<sub>2</sub> from both chemical bonding and microscopic perspectives. The results of rheological experiments indicated that the addition of nanoparticles improved the yield stress and long-term thermal stability of the gel. The scanning electron microscope (SEM) microstructure analysis confirmed that the addition of nanoparticles resulted in high-density cavities between the microscopic network structures of the gel. This facilitated the trapping of a significant amount of free water and the formation of a stable spatial mechanical support structure, ultimately enhancing the macro-mechanical strength of the gel. Additionally, FTIR and NMR experiments demonstrated that the nanoparticles effectively inhibited the hydrolysis of amide groups to carboxylate, thereby significantly preventing the high-temperature degradation of the gel and maintaining its strength after prolonged aging.</p><h3>Graphical abstract</h3>\\n<div><figure><div><div><picture><source><img></source></picture></div></div></figure></div></div>\",\"PeriodicalId\":520,\"journal\":{\"name\":\"Colloid and Polymer Science\",\"volume\":null,\"pages\":null},\"PeriodicalIF\":2.2000,\"publicationDate\":\"2024-04-14\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Colloid and Polymer Science\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://link.springer.com/article/10.1007/s00396-024-05253-y\",\"RegionNum\":4,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q3\",\"JCRName\":\"CHEMISTRY, PHYSICAL\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Colloid and Polymer Science","FirstCategoryId":"92","ListUrlMain":"https://link.springer.com/article/10.1007/s00396-024-05253-y","RegionNum":4,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"CHEMISTRY, PHYSICAL","Score":null,"Total":0}
Preparation and temperature resistance mechanism of nanoparticle-enhanced polymer gel
In order to solve the problem of poor stability of HPAM (partially hydrolyzed polyacrylamide) gel as a plugging agent at 150 °C, this paper investigates the preparation of a polymer gel strengthened with nano-SiO2, exhibiting good thermal stability, using a low-cost, low-hydrolysis anionic polymer. The experimental results indicated that when the gel was prepared with 1 wt% HPAM, 1 wt% water-soluble phenolic resin (WSPR) as a crosslinker, and 1 wt% nano-SiO2 as a stabilizer, the dehydration rate of the gel was less than 5 wt% after 180 days of aging at 150 °C. In order to identify the stability mechanism of nano-SiO2-strengthened polymer gel, we conducted rheological tests, Cryo-SEM analysis, Fourier transform infrared (FTIR) spectroscopy, and solid-state nuclear magnetic resonance (NMR) analysis on the polymer gel before and after adding nanoparticles. The methods described in the study demonstrate the excellent long-term thermal stability of the polymer gel strengthened with nano-SiO2 from both chemical bonding and microscopic perspectives. The results of rheological experiments indicated that the addition of nanoparticles improved the yield stress and long-term thermal stability of the gel. The scanning electron microscope (SEM) microstructure analysis confirmed that the addition of nanoparticles resulted in high-density cavities between the microscopic network structures of the gel. This facilitated the trapping of a significant amount of free water and the formation of a stable spatial mechanical support structure, ultimately enhancing the macro-mechanical strength of the gel. Additionally, FTIR and NMR experiments demonstrated that the nanoparticles effectively inhibited the hydrolysis of amide groups to carboxylate, thereby significantly preventing the high-temperature degradation of the gel and maintaining its strength after prolonged aging.
期刊介绍:
Colloid and Polymer Science - a leading international journal of longstanding tradition - is devoted to colloid and polymer science and its interdisciplinary interactions. As such, it responds to a demand which has lost none of its actuality as revealed in the trends of contemporary materials science.