Standalone Block Copolymer Nanoballoons: Decoupling Self-Assembly from Implementation in Nanomanufacturing AITranslate
Abstract AITranslate
We report a facile method to produce isolatable hollow-core elastomeric vesicles, “nanoballoons”, prepared via block copolymer self-assembly in a polymer blend. Poly(isoprene-block-dimethylsiloxane) (PI–PDMS) diblock copolymers are blended with PDMS homopolymers (h-PDMS) as a “solvent” phase to template the self-assembly of PDMS-tethered vesicles with PI walls. The walls are subsequently crosslinked to yield mechanically stabilized elastomeric vesicles. The h-PDMS inner core and matrix are separated from the vesicles by dialysis to yield the matrix-free nanoballoons. These objects, 0.3–1 μm in diameter, can be further reincorporated into a crosslinkable PDMS. Throughout the self-assembly, recovery, and reincorporation processes we apply several techniques including solvent dispersion/dynamic light scattering (DLS) measurements, transmission electron microscopy (TEM)/energy-dispersive X-ray spectroscopy (EDS), and small-angle X-ray scattering (SAXS) to provide a consilient body of evidence that the nanoballoon morphology is retained. This work presents advanced nanomanufacturing schema that illustrate the decoupling of the thermodynamic and dynamic factors that govern macromolecular self-assembly from the environment in which the self-assembled objects are deployed.
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DOI:https://doi.org/10.1021/acsapm.2c00647
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We report a facile method to produce isolatable hollow-core elastomeric vesicles, “nanoballoons”, prepared via block copolymer self-assembly in a polymer blend. Poly(isoprene-block-dimethylsiloxane) (PI–PDMS) diblock copolymers are blended with PDMS homopolymers (h-PDMS) as a “solvent” phase to template the self-assembly of PDMS-tethered vesicles with PI walls. The walls are subsequently crosslinked to yield mechanically stabilized elastomeric vesicles. The h-PDMS inner core and matrix are separated from the vesicles by dialysis to yield the matrix-free nanoballoons. These objects, 0.3–1 μm in diameter, can be further reincorporated into a crosslinkable PDMS. Throughout the self-assembly, recovery, and reincorporation processes we apply several techniques including solvent dispersion/dynamic light scattering (DLS) measurements, transmission electron microscopy (TEM)/energy-dispersive X-ray spectroscopy (EDS), and small-angle X-ray scattering (SAXS) to provide a consilient body of evidence that the nanoballoon morphology is retained. This work presents advanced nanomanufacturing schema that illustrate the decoupling of the thermodynamic and dynamic factors that govern macromolecular self-assembly from the environment in which the self-assembled objects are deployed.
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| GB/T 7714-2015 | [1] Tungping Wang, Liyang Shen, FangYi Lin, et al. ACS Applied Polymer Materials, 2022(4). DOI:10.1021/acsapm.2c00647. |
| MLA | [1] Tungping Wang, et al., ACS Applied Polymer Materials, no. 4, 2022, https://doi.org/10.1021/acsapm.2c00647. |
| APA | [1] Tungping Wang, Liyang Shen, FangYi Lin, Michael Forrester, Sabrina W. Torres, Thomas W. Robison, TingHan Lee, Shailja Goyal, & Eric W. Cochran. (2022). ACS Applied Polymer Materials(4). https://doi.org/10.1021/acsapm.2c00647 |
| IEEE | [1] Tungping Wang, Liyang Shen, FangYi Lin, Michael Forrester, Sabrina W. Torres, Thomas W. Robison, TingHan Lee, Shailja Goyal, and Eric W. Cochran, ACS Applied Polymer Materials, no. 4, 2022, doi: 10.1021/acsapm.2c00647. keywords: {elastomeric vesicles;nanoballoons;polymer blend;nanocomposite;block copolymers} |
