CO2-Switchable Multi-Stimuli-Responsive Polymer Nanoparticle Dispersion
Source abstract
Abstract
CO2-switchable multi-stimuli-responsive polymer nanoparticles (MSPNs), a combination of protonated poly(2-dimethylamino-ethyl methacrylate) (PDMAEMA) and hydrophobic poly(methyl methacrylate) (PMMA), were prepared by carbon-dioxide-assisted (CO2-assisted) emulsion polymerization. These MSPNs exhibited excellent thermal properties and unique temperature-/pH-responsive and CO2-/nitrogen-switchable (CO2-/N2-switchable) abilities, making them highly attractive multifunctional polymer nanoparticles with potential for many applications. Importantly, dispersion experiments and morphological studies clearly confirmed that these newly developed nanoparticles not only possess efficient, reversible CO2-/N2-switchable aggregation/redispersion ability, but also can remain in stable colloidal dispersion at low pH and promote rapid precipitation of nanoparticles at high pH. With simple preparation and high reproducibility, this approach provides a potentially novel pathway for the development of next-generation multifunctional MSPNs.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Advanced Polymer Synthesis and Characterization · Covalent Organic Framework Applications · Membrane Separation and Gas Transport
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Department of Chemical and Materials Engineering, National University of Kaohsiung, 700 Kaohsiung University Road, Nanzih District, Kaohsiung 81148, Taiwan
Graduate Institute of Applied Science and Technology, National Taiwan University of Science and Technology, 43 Keelung Road, Sec. 4, Da’an District, Taipei 10607, Taiwan
Funding
Ministry of Science and Technology, Taiwan
References (35)
Show source-provided references
1. 10.1038/nmat261410.1038/nmat2614 ↗
2. 10.1039/c2cs35091b10.1039/c2cs35091b ↗
3. 10.1038/nmat377610.1038/nmat3776 ↗
4. 10.1016/j.biomaterials.2013.01.08410.1016/j.biomaterials.2013.01.084 ↗
5. 10.1021/ar500045610.1021/ar5000456 ↗
6. 10.1002/tcr.20150028110.1002/tcr.201500281 ↗
7. 10.1039/C3PY00880K10.1039/C3PY00880K ↗
8. 10.1016/j.biomaterials.2009.11.07710.1016/j.biomaterials.2009.11.077 ↗
9. 10.1016/S1369-7021(12)70165-710.1016/S1369-7021(12)70165-7 ↗
10. 10.1021/ma302648w10.1021/ma302648w ↗
11. 10.1021/acs.langmuir.5b0344810.1021/acs.langmuir.5b03448 ↗
12. 10.1021/ma062199r10.1021/ma062199r ↗
13. 10.1021/mz200017510.1021/mz2000175 ↗
14. 10.1126/science.112814210.1126/science.1128142 ↗
15. 10.1038/4361102a10.1038/4361102a ↗
16. 10.1021/ma301518910.1021/ma3015189 ↗
17. 10.1039/C4SM02242D10.1039/C4SM02242D ↗
18. 10.1021/jp100714j10.1021/jp100714j ↗
19. 10.1016/j.polymer.2015.01.01710.1016/j.polymer.2015.01.017 ↗
20. 10.1021/mz300321510.1021/mz3003215 ↗
21. 10.1021/ma102936a10.1021/ma102936a ↗
22. 10.1021/ma200249q10.1021/ma200249q ↗
23. 10.1021/ma202748410.1021/ma2027484 ↗
24. 10.1021/ma800544v10.1021/ma800544v ↗
25. 10.1021/ma200592610.1021/ma2005926 ↗
26. 10.1021/acs.macromol.5b0185310.1021/acs.macromol.5b01853 ↗
27. 10.1021/acs.macromol.6b0211110.1021/acs.macromol.6b02111 ↗
28. 10.1002/marc.20120003310.1002/marc.201200033 ↗
29. 10.1002/mren.20160003510.1002/mren.201600035 ↗
30. 10.1039/C4CC03412K10.1039/C4CC03412K ↗
31. 10.1016/j.polymer.2016.08.06710.1016/j.polymer.2016.08.067 ↗
32. 10.1039/C5CS00873E10.1039/C5CS00873E ↗
33. 10.1021/jacs.7b0730310.1021/jacs.7b07303 ↗
34. 10.1002/adsu.20170005110.1002/adsu.201700051 ↗
35. 10.1021/ma980689g10.1021/ma980689g ↗