journal article·2016-03-02

Grafting PMMA Brushes from α-Alumina Nanoparticles via SI-ATRP

Amir Khabibullin, Karan Bhangaonkar, Clare Mahoney, Zhao Lu, Michael Schmitt, Ali Kemal Sekizkardes, Michael R. Bockstaller, Krzysztof Matyjaszewski

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Abstract

Alumina nanoparticles are widely used as nanofillers for polymer nanocomposites. Among several different polymorphs of alumina, α-alumina has the most desirable combination of physical properties. Hence, the attachment of polymer chains to α-alumina to enhance compatibility in polymeric matrixes is an important goal. However, the chemical inertness and low concentration of surface hydroxyl groups have rendered polymer modification of α-alumina a long-standing challenge. Herein, we report that activation of α-alumina in concentrated or molten NaOH as well as in molten K2S2O7 increased polymer graft density up to 50%, thereby facilitating the synthesis of α-alumina brush particles with uniform grafting density of 0.05 nm(-2) that are readily miscible or dispersible in organic solvents or in chemically compatible polymeric hosts.
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Research context

OpenAlex topics: Polymer Surface Interaction Studies · Polymer Nanocomposites and Properties · Polymer Nanocomposite Synthesis and Irradiation

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

Affiliations

Department of Chemistry, Carnegie Mellon University, 4400 Fifth Ave, Pittsburgh, Pennsylvania 15213, United States

Department of Materials Science and Engineering, Carnegie Mellon University, 5000 Forbes Avenue, Pittsburgh, Pennsylvania, 15213, United States

National Energy and Technology Lab (NETL), U.S. Department of Energy, 626 Cochrans Mill Rd, Pittsburgh, Pennsylvania 15129, United States

Funding

U.S. Department of Energy · Division of Materials Research

References (39)

Show source-provided references
1. 10.1007/12_2014_28510.1007/12_2014_285 ↗
2. 10.1021/cm402363410.1021/cm4023634 ↗
3. 10.1016/j.polymer.2008.04.01710.1016/j.polymer.2008.04.017 ↗
4. 10.1039/c4nr01788a10.1039/c4nr01788a ↗
5. 10.1021/cr068035q10.1021/cr068035q ↗
6. 10.1039/b819615j10.1039/b819615j ↗
7. 10.1021/am405332a10.1021/am405332a ↗
8. 10.1021/cm990537f10.1021/cm990537f ↗
9. 10.1039/C0PY00284D10.1039/C0PY00284D ↗
10. 10.1039/c1jm11443c10.1039/c1jm11443c ↗
11. Advincula R. C. · 2009 · 3417
12. 10.1039/C5CP01032B10.1039/C5CP01032B ↗
13. 10.1016/j.progpolymsci.2015.07.00410.1016/j.progpolymsci.2015.07.004 ↗
14. 10.1021/ma035440010.1021/ma0354400 ↗
15. 10.1002/polb.2029710.1002/polb.20297 ↗
16. Lynch C. T. · 1975
17. 10.1021/la503703710.1021/la5037037 ↗
18. 10.1021/la401522v10.1021/la401522v ↗
19. 10.1016/j.polymer.2014.03.00510.1016/j.polymer.2014.03.005 ↗
20. 10.1002/pat.115710.1002/pat.1157 ↗
21. 10.1007/12_2015_31110.1007/12_2015_311 ↗
22. 10.1021/cm011065j10.1021/cm011065j ↗
23. 10.1021/ma991146p10.1021/ma991146p ↗
24. 10.1021/ja408069v10.1021/ja408069v ↗
25. 10.1021/ma300171910.1021/ma3001719 ↗
26. 10.1021/la063402e10.1021/la063402e ↗
27. 10.1021/ma801643r10.1021/ma801643r ↗
28. 10.1002/marc.20100053110.1002/marc.201000531 ↗
29. 10.1016/j.apsusc.2011.08.12110.1016/j.apsusc.2011.08.121 ↗
30. 10.1021/ja311918z10.1021/ja311918z ↗
31. 10.1021/la304949h10.1021/la304949h ↗
32. 10.1021/ma020809r10.1021/ma020809r ↗
33. 10.1246/cl.2010.119010.1246/cl.2010.1190 ↗
34. 10.1021/acsami.5b0642710.1021/acsami.5b06427 ↗
35. 10.1021/ma048011q10.1021/ma048011q ↗
36. 10.1039/C5PY01521A10.1039/C5PY01521A ↗
37. 10.1134/S002016851014001310.1134/S0020168510140013 ↗
38. 10.1021/acs.macromol.5b0190510.1021/acs.macromol.5b01905 ↗
39. 10.1007/s10904-006-9043-x10.1007/s10904-006-9043-x ↗