Effects of synthesis-solvent polarity on the physicochemical and rheological properties of poly(N-isopropylacrylamide) (PNIPAm) hydrogels

被引:30
|
作者
Rana, Md Mohosin [1 ]
Rajeev, Ashna [2 ]
Natale, Giovanniantonio [2 ]
Siegler, Hector De la Hoz [1 ,2 ]
机构
[1] Univ Calgary, Schulich Sch Engn, Biomed Engn Grad Program, Calgary, AB T2N 1N4, Canada
[2] Univ Calgary, Schulich Sch Engn, Dept Chem & Petr Engn, Calgary, AB T2N 1N4, Canada
基金
加拿大创新基金会;
关键词
Synthesis-solvent; Polarity; PNIPAm; Swelling behavior; Microstructure; Rheology; FREE-RADICAL POLYMERIZATION; N-ISOPROPYLACRYLAMIDE; RATE CONSTANTS; THERMORESPONSIVE POLYMERS; DRUG-DELIVERY; CROSS-LINKING; TRANSITION TEMPERATURE; ABSTRACTION REACTIONS; SWELLING BEHAVIOR; MIXED-SOLVENTS;
D O I
10.1016/j.jmrt.2021.05.009
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
Thermoresponsive poly(N-isopropylacrylamide) (PNIPAm) microgels were synthesized via free radical polymerization using four synthesis-solvents with varying polarity index: dioxane, tetrahydrofuran (THF), toluene, and cyclohexane. Characterization by FTIR, NMR, and XRD confirmed the chemical structure of synthesized PNIPAm microgels. Microgels synthesized in polar solvents have a lower degree of porosity and display lower swelling values (around 275% and 314% for THF and dioxane, respectively). In contrast, microgels synthesized in the nonpolar solvents toluene and cyclohexane have a higher degree of porosity and a higher degree of swelling (about 900% for cyclohexane). From the dynamic rheology study, the best mechanical performance was obtained with the microgels synthesized in dioxane and toluene due to their unique crosslinked structure. Considering their higher porosity, degree of swelling, thermal stability, and mechanical properties, this study confirms that microgels synthesized in nonpolar solvent like toluene can be an attractive option for multiple applications. (c) 2021 The Author(s). Published by Elsevier B.V. This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
引用
收藏
页码:769 / 786
页数:18
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