Multi-Stimuli-Responsive Polymer/Inorganic Janus Composite Nanoparticles
Source abstract
Abstract
Multi-stimuli-responsive Janus composite nanoparticles (JNPs) of poly(N-isopropylacrylamide)–Fe3O4–poly(2-(dimethylamino)ethyl methacrylate)) (PNIPAM–Fe3O4–PDMEAMA) are synthesized by sequential reversible addition–fragmentation chain-transfer grafting of the polymer PNIPAM and atom-transfer radical polymerization grafting of the polymer PDMEAMA from the corresponding sides of modified Fe3O4 nanoparticles of ∼10 nm size. The hydrophilic/amphiphilic/hydrophobic reversible transition of the JNP can be triggered by pH and temperature since the wettability of the two polymers on the opposite sides is tunable accordingly. At a high pH value and a low surrounding temperature, applying near-infrared irradiation will induce the amphiphilic/hydrophobic transition owing to the photothermal effect of Fe3O4 NPs. The JNP can serve as a responsive solid emulsifier, and the stability and microstructure of the emulsions can be easily controlled by external stimuli such as the pH, temperature, and magnetic field.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Pickering emulsions and particle stabilization · Surfactants and Colloidal Systems · Advanced Polymer Synthesis and Characterization
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Department of Materials Science, Fudan University, Shanghai 200433, China
Zhuhai Fudan Innovation Institute, Zhuhai 518057, China
School of Light Industry and Engineering, South China University of Technology, Guangzhou 510641, China
Funding
Guangdong Basic and Applied Basic Research Foundation · Zhuhai Basic and Applied Basic Research Foundation
References (25)
Show source-provided references
1. 10.1007/s00396-020-04601-y10.1007/s00396-020-04601-y ↗
2. 10.1007/s00396-017-4192-810.1007/s00396-017-4192-8 ↗
3. 10.1016/j.progpolymsci.2017.07.00510.1016/j.progpolymsci.2017.07.005 ↗
4. 10.1002/marc.20170003010.1002/marc.201700030 ↗
5. 10.1002/ppsc.20130014610.1002/ppsc.201300146 ↗
6. 10.1021/jacs.9b1020510.1021/jacs.9b10205 ↗
7. 10.1016/j.nantod.2018.08.00910.1016/j.nantod.2018.08.009 ↗
8. 10.1021/acsmacrolett.5b0032110.1021/acsmacrolett.5b00321 ↗
9. 10.1016/j.jconrel.2018.07.04110.1016/j.jconrel.2018.07.041 ↗
10. 10.1021/acs.chemrev.5b0029010.1021/acs.chemrev.5b00290 ↗
11. 10.31635/ccschem.019.2019003510.31635/ccschem.019.20190035 ↗
12. 10.1021/acs.macromol.9b0238810.1021/acs.macromol.9b02388 ↗
13. 10.1021/acs.macromol.6b0200410.1021/acs.macromol.6b02004 ↗
14. 10.1021/acs.macromol.0c0010910.1021/acs.macromol.0c00109 ↗
15. 10.1016/j.nantod.2011.04.00810.1016/j.nantod.2011.04.008 ↗
16. 10.1039/c9cc03067k10.1039/c9cc03067k ↗
17. 10.1021/acs.langmuir.6b0056210.1021/acs.langmuir.6b00562 ↗
18. 10.1021/ja804192e10.1021/ja804192e ↗
19. 10.1021/jacs.5b0979010.1021/jacs.5b09790 ↗
20. 10.1016/j.polymer.2017.09.06810.1016/j.polymer.2017.09.068 ↗
21. 10.1021/nn800089z10.1021/nn800089z ↗
22. 10.1021/ja074052110.1021/ja0740521 ↗
23. 10.1016/0021-9797(68)90272-510.1016/0021-9797(68)90272-5 ↗
24. 10.1016/j.apsusc.2008.01.16710.1016/j.apsusc.2008.01.167 ↗
25. 10.1021/ma400261y10.1021/ma400261y ↗