Effect of ion-dipole interaction on the formation of polar extended-chain crystals in high pressure-crystallized poly(vinylidene fluoride). (5th December 2018)
- Record Type:
- Journal Article
- Title:
- Effect of ion-dipole interaction on the formation of polar extended-chain crystals in high pressure-crystallized poly(vinylidene fluoride). (5th December 2018)
- Main Title:
- Effect of ion-dipole interaction on the formation of polar extended-chain crystals in high pressure-crystallized poly(vinylidene fluoride)
- Authors:
- Ren, Jia-Yi
Zhang, Guoqiang
Li, Yue
Lei, Jun
Zhu, Lei
Zhong, Gan-Ji
Li, Zhong-Ming - Abstract:
- Abstract: The manipulation of crystal superstructure and polymorphism of poly(vinylidene fluoride) (PVDF) are of great technical importance to expand its applications in flexible electronics. In this work, strong ion-dipole interaction via the introduction of cetyltrimethylammonium bromide (CTAB) in PVDF induced zig-zag conformers [i.e., the precursor nuclei of β/γ folded chain crystals (FCCs)]. Meanwhile, favorable conditions (i.e., high temperature and high pressure) for the pseudohexagonal (hex) paraelectric (PE) phase with gauche conformers [i.e., the precursor nuclei of extended-chain crystals (ECCs)] are purposely chosen to study whether there is any synergy between the ion-dipole interaction and ECCs. It is interesting to find that the high pressure/high temperature hex PE phase can be substantially affected by the strong ion-dipole interaction between PVDF and CTAB. For the neat PVDF melt, most hexagonal folded-chain (h-FC) nuclei ultimately lead to major β/γ ECCs. For the PVDF melt with 5 wt% CTAB, the β/γ FC nuclei induced by the strong ion-dipole interaction compete with the h-FC nuclei at the initial nucleation stage. The β/γ FC nuclei are found to be more kinetically favorable in the beginning under a high pressure, leading to major β/γ FCCs and minor β/γ ECCs. Furthermore, compared to neat PVDF, addition of 5 wt% CTAB resulted in ECCs of a thinner lamellar thickness. Finally, this new understanding leads to a modified T-P phase diagram, in which the kineticallyAbstract: The manipulation of crystal superstructure and polymorphism of poly(vinylidene fluoride) (PVDF) are of great technical importance to expand its applications in flexible electronics. In this work, strong ion-dipole interaction via the introduction of cetyltrimethylammonium bromide (CTAB) in PVDF induced zig-zag conformers [i.e., the precursor nuclei of β/γ folded chain crystals (FCCs)]. Meanwhile, favorable conditions (i.e., high temperature and high pressure) for the pseudohexagonal (hex) paraelectric (PE) phase with gauche conformers [i.e., the precursor nuclei of extended-chain crystals (ECCs)] are purposely chosen to study whether there is any synergy between the ion-dipole interaction and ECCs. It is interesting to find that the high pressure/high temperature hex PE phase can be substantially affected by the strong ion-dipole interaction between PVDF and CTAB. For the neat PVDF melt, most hexagonal folded-chain (h-FC) nuclei ultimately lead to major β/γ ECCs. For the PVDF melt with 5 wt% CTAB, the β/γ FC nuclei induced by the strong ion-dipole interaction compete with the h-FC nuclei at the initial nucleation stage. The β/γ FC nuclei are found to be more kinetically favorable in the beginning under a high pressure, leading to major β/γ FCCs and minor β/γ ECCs. Furthermore, compared to neat PVDF, addition of 5 wt% CTAB resulted in ECCs of a thinner lamellar thickness. Finally, this new understanding leads to a modified T-P phase diagram, in which the kinetically favorable area for α/β/γ FC nucleation expands to higher temperatures because of the strong ion-dipole interaction. Graphical abstract: Highlights: The β/γ FC nuclei induced by strong ion-dipole interaction are kinetically favorable at the initial nucleation stage. The strong ion-dipole interaction suppressed lamellar thickening resulting in thinner lamellar thickness of β/γ ECCs. A modified T-P phase diagram reveals the effect of ion-dipole interaction on the formation of polar extended-chain crystals. … (more)
- Is Part Of:
- Polymer. Volume 158(2018)
- Journal:
- Polymer
- Issue:
- Volume 158(2018)
- Issue Display:
- Volume 158, Issue 2018 (2018)
- Year:
- 2018
- Volume:
- 158
- Issue:
- 2018
- Issue Sort Value:
- 2018-0158-2018-0000
- Page Start:
- 204
- Page End:
- 212
- Publication Date:
- 2018-12-05
- Subjects:
- Poly(vinylidene fluoride) -- Ion-dipole interaction -- High pressure crystallization -- Extended-chain crystals
Polymers -- Periodicals
Polymerization -- Periodicals
Polymères -- Périodiques
Polymérisation -- Périodiques
547.7 - Journal URLs:
- http://www.sciencedirect.com/science/journal/00323861 ↗
http://www.elsevier.com/journals ↗ - DOI:
- 10.1016/j.polymer.2018.10.063 ↗
- Languages:
- English
- ISSNs:
- 0032-3861
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 6547.700000
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 8754.xml