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Article

Morphology, Mechanical Properties and Shape Memory Effects of Polyamide12/Polyolefin Elastomer Blends Compatibilized by Glycidylisobutyl POSS

by
Dong-Hun Lee
1,
Young-Wook Chang
1,2,* and
Keon-Soo Jang
3
1
Department of Materials & Chemical Engineering, Hanyang University, Ansan, Gyeonggi-do 15588, Korea
2
BK21 FOUR ERICA-ACE Center, Hanyang University, Ansan, Gyeonggi-do 15588, Korea
3
Department of Polymer Engineering, School of Chemical and Materials Engineering, The University of Suwon, Hwaseong, Gyeonggi-do 18323, Korea
*
Author to whom correspondence should be addressed.
Materials 2021, 14(1), 27; https://doi.org/10.3390/ma14010027
Submission received: 14 November 2020 / Revised: 18 December 2020 / Accepted: 21 December 2020 / Published: 23 December 2020
(This article belongs to the Special Issue Polymer Blends: Processing, Morphology, and Properties)
Browse Figures
Versions Notes

Abstract

:
Small amounts of glycidylisobutyl polyhedral oligomericsilsesquioxane (G-POSS) (up to 10 phr) were added into a immiscible polyamide12 (PA12)/polyolefin elastomer (POE) blend (70 wt%/30 wt%) by simple melt mixing. The effects of the G-POSS on phase morphology and mechanical properties were investigated by FE-SEM, tensile testing, Izod impact test and dynamic mechanical analysis. FE-SEM analysis revealed that domain size of the dispersed POE phase in matrix PA12 is decreased significantly by adding the G-POSS, indicating a compatibilization effect of the G-POSS for the immiscible PA12/POE blend. The PA12/POE blend compatibilized with POSS showed simultaneous enhancement in mechanical properties including tensile modulus, strength and toughness. Further, thermally triggered shape memory effect was observed in this compatibilized blend.

1. Introduction

Polymer blending is an efficient and simple way to develop new polymeric materials possessing desirable physical properties and specific functionalities for various end-use applications. Most of the polymer blends are immiscible and need proper compatibilization in order to obtain proper phase separated morphologies which determine the performance properties. The compatibilization induces finer phase morphology by improving interfacial adhesion between the component polymers in the blend, which promotes their synergistic combination [1,2].
Blends of polyamides (PA) with polyolefins (PO) are important class of polymer blends because of their balanced properties of strength, toughness and moisture resistance. For the compatibizations of the immiscible PA/PO blends, functionalized polyolefins, such as maleic anhydride (MA)-grafted polyolefins, have been investigated [3,4,5,6,7,8]. Recently, it has been reported that phase morphology and properties of the immiscible PA/PO blends can be influenced by the addition of inorganic nanoparticles such as clay [9], silica [10], carbon nanotube [11], alumina [12] and POSS [13]. The nanoparticles are located at the interface between the component polymers or in one component selectively, which affect the phase morphology of the blends.
Among various inorganic nanofillers, polyhedral oligomeric silsesquioxane (POSS) is unique which features a well-defined nanosized Si–O cage structure (Si8O12) with additional organic functional groups covalently bonded to each vertex Si on the cage. Due to the organic functional groups, the POSS cage is naturally compatible with polymers, and can be chemically bonded to polymer chain [14,15,16]. The POSS can be added into various thermoplastics such as polyolefins [17,18,19], polyamides [20,21,22] and others [23,24,25] by melt blending using conventional high-shear mixer and induced improved thermal stability and mechanical properties of the matrix polymer. As compared to the POSS nanocomposites with a single polymer matrix, relatively less studies on those with immiscible polymer blends have been reported [13,26,27].
Polyamide12 (PA12) is one of the important engineering plastics with a broad range of applications including oil resistant tubes for automotive, cables, food packaging films and powder coatings for metals. For the improvement in toughness of the PA12, blending it with various rubbers such as styrene/ethylene-butylene/styrene block (SEBS) rubber [28], epoxidized natural rubber (ENR) [29] and natural rubber [30] has been explored However, this decreases the tensile modulus and strength. Polyolefin elastomer (POE), a commercially important rubber developed by Dow Elastomers under the brand name Engage®, has good processibility and thermo-oxidative resistance. To the best of our knowledge, studies on PA12/POE blend with simultaneously improved toughness and strength, which endow the material to have advantages in practical applications, have not been reported yet.
Hence, this work employed glycidylisobutyl POSS (G-POSS) having a cage structure with one glycidyl and seven isobutyl groups at each corner of the cage (Figure 1) as a compatibilizer and reinforcing nanofiller for immiscible PA12/POE blend. The G-POSS was expected to act as a compatibilizer for the blend due to its affinity with both component polymers via reaction of its glycidyl group with end reactive groups (–NH2 or –COOH) of PA12 during melt mixing and van der Waals interaction of isobutyl groups with POE, respectively. The compatibilization and reinforcing effects of the G-POSS for the PA12/POE (70 wt%/30 wt%) blend were investigated by observation of phase morphology and mechanical properties. A thermally-triggered shape memory effect of this blend is also reported.

2. Materials and Methods

2.1. Materials and Sample Preparation

PA12 (Rilsan AESNO TL) was purchased from Arkema (Paris, France). POE (Engage 8842, Dow Chemical Co., Midland, MI, USA) was obtained from Dow Chemical Co., USA. Glycidylisobutyl POSS (G-POSS, EP0418) was purchased from Hybrid Plastics Co (Hattiesburg, MS, USA).
PA12/POE (70 wt%/30 wt%) blends with G-POSS content of up to 10 part per hundred (phr) of the polymers were prepared by melt mixing at 200 °C in a Haake internal mixer equipped with a cam rotor (Haake Polylab Rheomix 600, Karlsruhe, Germany) at a rotor speed of 60 rpm. PA12 was first melted for 1 min followed by addition of POE and mixed for another 1 min, then desired amount of G-POSS was loaded and mixed into the mixture and mixing continued for 10 min till the mixing torque was stabilized. The obtained PA12/POE/G-POSS mixture was formed into a sheet by compression molding at 200 °C in an electrically heated press (Carver 2518, Wabash, IN, USA) for the property measurements.

2.2. Characterization

2.2.1. FE-SEM Analysis

Phase morphologies of the blend were investigated by a field emission-scanning electron microscope (FE-SEM, S-900, Hitachi Co., Tokyo, Japan) at an accelerating voltage of 15 kV. To avoid ductile deformation during fracture, the samples were chilled in liquid nitrogen before breaking to initiate a brittle fracture. The cryogenically fractured surface was sputter-coated with platinum prior to SEM observation.

2.2.2. Tensile Test

Tensile properties were measured at 25 °C using a universal testing machine (STM-10E, United Co., Fullerton, CA, USA) at a crosshead speed of 50 mm/min with an initial gauge length of 20 mm. At least five specimens were used for the test. Elastic moduli were obtained from the initial slope of the stress–strain curves (up to about 1% strain). Tensile toughness of each sample was obtained by calculating the area of the stress–strain curves.

2.2.3. Izod Impact Test

Notched Izod impact strength was measured using a sample with a thickness of 4 mm and width of 10 mm at 25 °C using an impact tester (DYC-103C, Daeyeong MTC, Hwaseong, South Korea) according to ISO 180. The test was conducted using 10 specimens, and the average values are presented here.

2.2.4. Dynamic Mechanical Analysis

Dynamic storage modulus and tan δ as a function of temperature were determined using a dynamic mechanical analyzer (DMA2980, TA Instruments, New Castle, DE, USA) under a cyclic tensile strain with an amplitude of 10% at a frequency of 1 Hz. The temperature increased at a heating rate of 2 °C min−1 from −100 to 200 °C.

2.2.5. Evaluation of Thermally-Triggered Shape Memory Effects

In order to evaluate thermally-triggered shape memory behavior of the samples, temporarily-fixed sample obtained by uniaxial deformation of dogbone-shaped specimen with a thickness of ca. 1 mm to 50% at 70 °C (which is just above Tg and well below Tm of the blend) followed by cooling the deformed shape to 0 °C was heated to 70 °C. The shape fixing ratio (Rf) and shape recovery ratio (Rr) of samples were determined by following equations, respectively.
Shape fixing (%) = εu/εm × 100
Shape recovery (%) = [(εm − εp)/εm] × 100
where εm is an initial strain imposed onto the sample (50% in this case), εu is a strain measured upon cooling the deformed sample at 0 °C and εp is a strain measured upon heating the temporarily deformed shape at 70 °C.

3. Results and Discussions

3.1. Phase Morphology

SEM images of the blend with various amounts of POSS are shown in Figure 2. It can be seen that all blends have phase-separated morphologies, in which POE forms dispersed domain in PA12 matrix, and the dispersed domain size decreased with addition of a small amount of POSS. The dispersed domain size of POE phase with the amount of POSS are shown in Figure 3. It can be seen that the domain size decreased from 34 μm for unfilled blend to about 10 μm for the blend with 5 phr POSS, and then a slow but gradual decrease was observed with further increasing amount of the POSS. Similar trend was also observed in immiscible blend compatibilized with a block (or graft) copolymer [3] which are located at the interface between the component polymers. The G-POSS nanoparticles might have been located at the interface between PA12 and POE through reaction between glycidyl group of G-POSS with amine end group of PA12 during high shear mixing [13] and van der Waals interactions between alkyl group of POSS with POE [17]. This can prevent the coalescence of the dispersed rubber phase, thereby decreasing the rubber diameter. At G-POSS of higher than 5 phr, the competition between break-up and coalescence was maintained at the same level.

3.2. Mechanical Properties

Stress–strain curves of PA12/POE blend with various amounts of G-POSS are presented in Figure 4, and Young’s modulus, tensile strength, elongation-at-break and tensile toughness obtained from the curves are summarized in Table 1. The blend compatibilized by G-POSS reveals higher values in the modulus, tensile strength and elongation at break, as well as tensile toughness as compared to the blend without the POSS. The Izod impact strengths of the blend are also shown in the Table 1. It can also be seen that the Izod impact strength improved upon the loading of G-POSS into the blend. Tensile modulus, tensile toughness and Izod impact strength of the blend with 10 phr POSS increased by about 115%, 60% and 20% as compared to those of the blend without the POSS, respectively.
Such improved toughness of the blends compatibilized by the POSS is attributed to decrease in dispersed rubber particle sizes as observed in the SEM image as well as enhanced interfacial adhesion due to the G-POSS located at the interface between the component polymers. In addition, the rigid POSS nanoparticles acted as a reinforcing filler for the PA12/POE blends and led to enhancement in strength and modulus. In other words, compatibilizing action of the rigid POSS nanoparticles resulted in outstanding simultaneous enhancement in strength and toughness. Similar simultaneous enhancements in reinforcement and toughness were also observed in other rubber toughened polymer blends containing inorganic nanoparticles [31,32].

3.3. Dynamic Mechanical Properties

Figure 5a,b show temperature dependence of dynamic storage moduli and tan δ of the samples, respectively. As shown in Figure 5a, the storage moduli of the blend compatibilized by POSS are higher than those of the neat blend over the whole temperature range examined here, and the modulus increased with increasing G-POSS content. The storage modulus at 30 ℃, for example, was enhanced from 296 MPa for unfilled blend to 564 MPa (about 100% increase) for the blend loaded with 10 phr POSS. Such enhancement is correlated with an increase in tensile modulus, which is attributed to finer dispersion of rubber particle due to the compatibilization by the G-POSS and rigid nature of the POSS nanoparticles in the blend. It is also to be noted that all samples exhibit persistent plateau before the temperature reaches 170 °C at which crystalline domains of PA12 are melted.
Variation of tan δ with temperature is shown in Figure 5b. The two peaks appeared in all samples, which are attributed to glass-to-rubber transition of the POE (lower temperature) and PA12 (higher temperature), respectively. The glass transition temperatures (tan δ peak maximum) of the blend samples are shown in Table 2. It can be seen from the table that Tg of PA12 phase was shifted towards the lower value with the incorporation of POSS into the blend, from 47.1 °C in the neat PA12/POE blend to 41.8 °C in the blend with POSS content of 10 phr. The lowering of Tg of PA12 phase is due to interfacial compatibilization between the PA12 with POE by the G-POSS, which resulted in increased amorphous portion of PA12 [3,4]. Lowering of Tg of POE phase in the presence of POSS was probably due to the plasticization effect of isobutyl group of the G-POSS.

3.4. Shape Memory Effects

We observed a shape memory effect in these blends, as demonstrated in Figure 6 and in Table 3. All the temporarily elongated samples shrank and recovered to their original shape upon heating above Tg of the PA12 phase. The recovery ratio increased with increasing POSS content from 47.5% for the blend without the POSS to 94% for the blend with 10 phr POSS.
Shape memory polymers have two structural features, i.e., the cross-links that determine the permanent shape and the reversible segments acting as a switching phase [33,34]. Blend of semicrystalline PA12 with elastomer studied here have these structural features, in which PA12 crystallites with Tm of about 175 °C act as crosslink points while amorphous chain of PA12 with Tg of about 40~47 °C act as the reversible phase. When the blend was deformed under tensile load above its Tg, amorphous regions are oriented and elastic energy is stored during the deformation. The stored elastic energy is released when the blends are heated above its Tg, which renders the molecules to have an activity and to recover to its original shape instantaneously upon heating above the Tg and well below crystalline melting temperature. The same structural features have been reported for semicrystalline polymers like PLA [35,36] and PVDF [37] with thermally triggered shape memory effects. Amorphous portions of these semicrystalline polymer molecules can be oriented in direction to applied force at temperature higher than its Tg and much lower than its Tm, and the deformed shape can be fixed as a temporary shape upon cooling below T < Tg due to trapping the entropy of the chains. When the temporarily fixed sample is heated above Tg, the shape recovery occurs due to the release of stored entropic energy and the relaxation of the polymer molecular chains to a higher entropic state. Therefore, the driving force of shape recovery mainly stems from the elastic resilience of the elongated polymer molecular chains. This is the molecular mechanism for the inherent shape memory properties of these semicrystalline polymers. It is also to be noted that blending of these semicrystalline polymers with elastomers along with proper compatibilization can promote the orientation and reorganization of polymer chains.
The improved shape recovery of the PA12/POE blend compatibilized by POSS is correlated with the improved interfacial adhesion of PA12 with the elastomer as discussed above. The dispersed elastomer domains having good interfacial adhesion with the matrix PA12 allows the amorphous chains of the PA12 to have higher activity than those in the uncompatibilized blend and to recover to its original shape with the stress releasing instantaneously upon heating its Tg.
It should be emphasized that the PA12 blend with shape memory effect and improved mechanical properties can be processed using conventional methods such as extrusion, melt spinning, injection molding and found diverse applications including heat shrinkable fibers, films, tubes as well as self-deployable and actuating devices. These materials in the form of powder are particularly suitable in metal coatings for corrosion protection as well as in powder-based 3D printing processes such as selective laser sintering (SLS) and high-speed sintering (HSS) for precise manufacturing of parts with complicated shape [38,39]. Further, this blend material can be processed with recently developed modern processing technologies, such as centrifugal spinning and pressurized gyration [40,41,42] to fabricate nonwoven shape memory webs in mass production scale for their applications in smart wearable devices, intelligent tools for biomedical applications, sensors, etc.

4. Conclusions

This study demonstrated that a POSS having both a glycidyl group and several alkyl groups on its cage can act as a compatibilizer for an immiscible PA12/POE (70 wt%/30 wt%) blend system. The incorporation of a small amount of G-POSS reduced the dispersed POE domain size in PA12 matrix of the blend. The combination of the decreased rubber particle size and the presence of rigid POSS nanoparticles in the blend led to interesting simultaneous improvement in modulus and toughness. Moreover, the PA12/POE blend embedded with POSS represented excellent thermally triggered shape memory effect. The PA12 blends with good mechanical properties and shape memory effects may have diverse applications such as smart packaging films, sensors, fast deployable and actuating devices. Further studies on the use of this material for modern processing technologies will be performed.

Author Contributions

Conceptualization, Y.-W.C.; data curation, D.-H.L. and K.-S.J.; formal analysis, D.-H.L. and K.-S.J.; writing—original draft preparation, Y.-W.C.; supervision, Y.-W.C.; writing—review and editing, Y.-W.C. and K.-S.J. All authors have read and agreed to the published version of the manuscript.

Funding

This research was funded by Ministry of Trade, Industry, and Energy, Republic of Korea (Project No: 10050842).

Data Availability Statement

The data presented in this study are available on request from the corresponding author. The data are not publicly available due to technical or time limitations at this time.

Conflicts of Interest

The authors declare no conflict of interest.

References

  1. Barlow, J.W.; Paul, D.R. Polymer blends and alloys-a review of selected considersations. Polym. Eng. Sci. 1981, 21, 985. [Google Scholar] [CrossRef]
  2. Utracki, L.A. Compatibilization of polymer blends. Can. J. Chem. Eng. 2002, 80, 1008–1016. [Google Scholar] [CrossRef] [Green Version]
  3. Favis, B.D. Phase size/interface relationships in polymer blends: The emulsification curve. Polymer 1994, 135, 1552–1555. [Google Scholar] [CrossRef]
  4. Gadekar, R.; Kulkarni, A.; Jog, J.P. Blends of nylon with polyethylene: Effect of compatibilization on mechanical and dynamic mechanical properties. J. Appl. Polym. Sci. 1998, 69, 161. [Google Scholar] [CrossRef]
  5. Okada, O.; Keskkula, H.; Paul, D.R. Mechanical properties of blends of maleated ethylene–propylene rubber and nylon 6. Polymer 2001, 42, 8715–8725. [Google Scholar] [CrossRef]
  6. Komalan, C.; George, K.E.; Jacob, S.; Thomas, S. Reactive compatibilization of nylon copolymer/EPDM blends: Experimental aspects and their comparison with theory. Polym. Adv. Technol. 2008, 19, 351–360. [Google Scholar] [CrossRef]
  7. Gonzalez-Montiel, A.; Keskkula, H.; Paul, D.R. Impact-modified nylon 6/polypropylene blends: 1. Morphology-property relationships. Polymer 1995, 36, 4587–4603. [Google Scholar] [CrossRef]
  8. La Mantia, F.P.; Ceraulo, M.; Mistretta, C.; Botta, L.; Morreals, M. Compatibilization of polypropylene/polyamide 6 blend fibers using photo-oxidized polypropylene. Materials 2019, 12, 81. [Google Scholar] [CrossRef] [Green Version]
  9. Khatua, B.B.; Lee, D.J.; Kim, H.Y.; Kim, J.K. Effect of organoclay platelets on morphology of nylon-6 and poly(ethylene-ran-propylene) rubber blends. Macromolecules 2004, 37, 2454–2459. [Google Scholar] [CrossRef]
  10. Zhang, B.; Wong, J.S.; Shi, D.; Yam, R.C.; Li, R.K. Investigation on the mechanical performances of ternary nylon 6/SEBS elastomer/nano-SiO2 hybrid composites with controlled morphology. J. Appl. Polym. Sci. 2010, 115, 469. [Google Scholar] [CrossRef]
  11. Xiang, F.; Shi, Y.; Li, X.; Huang, T.; Chen, C.; Peng, Y.; Wang, Y. Cocontinuous morphology of immiscible high density polyethylene/polyamide 6 blend induced by multiwalled carbon nanotubes network. Eur. Polym. J. 2012, 48, 350–361. [Google Scholar] [CrossRef]
  12. Ogunniran, E.S.; Sadiku, R.; Ray, S.S.; Luruli, N. Morphology and thermal properties of compatibilized PA12/PP blends with boehmite alumina nanofiller inclusions. Macromol. Mater. Eng. 2011, 29, 627–638. [Google Scholar] [CrossRef]
  13. Kodal, M. Polypropylene/polyamide 6/POSS ternary nanocomposites: Effects of POSS nanoparticles on the compatibility. Polymer 2016, 105, 43. [Google Scholar] [CrossRef]
  14. Wang, F.; Lu, X.; He, C. Some recent developments of polyhedral oligomeric silsesquioxane (POSS)-based polymeric materials. J. Mater. Chem. 2011, 21, 2775–2782. [Google Scholar] [CrossRef]
  15. Kuo, S.-W.; Chang, F.-C. POSS related polymer nanocomposites. Prog. Polym. Sci. 2011, 36, 1649–1696. [Google Scholar] [CrossRef]
  16. Ayandele, E.; Sarkar, B.; Alexandridis, P. Polyhedral oligomeric silsesquioxane (POSS)-containing polymer nanocomposites. Nanomaterials 2012, 2, 445–475. [Google Scholar] [CrossRef] [Green Version]
  17. Grala, M.; Bartczak, A. Morphology and mechanical properties of high density polyethylene-POSS hybrid nanocomposites obtained by reactive blending. Polym. Eng. Sci. 2015, 55, 2058–2072. [Google Scholar] [CrossRef]
  18. Fina, A.; Tabuani, D.; Frache, A.; Camino, G. Polypropylene–polyhedral oligomeric silsesquioxanes(POSS) nanocomposites. Polymer 2005, 46, 7855–7866. [Google Scholar] [CrossRef]
  19. Niemczyk, A.; Dziubek, K.; Sacher-Majewska, B.; Czaja, K.; Dutkiewicz, M.; Marciniec, B. Study of thermal properties of polyethylene and polypropylene nanocomposites with long alkyl chain-substituted POSS fillers. J. Therm. Anal. Cal. 2016, 125, 1287–1299. [Google Scholar] [CrossRef] [Green Version]
  20. Wan, C.; Zhao, F.; Bao, X.; Kandasubramanian, B.; Duggan, M. Effect of POSS on crystalline transitions and physical properties of polyamide 12. J. Polym. Sci. Part B Polym. Phys. 2009, 47, 121–129. [Google Scholar] [CrossRef]
  21. Misra, R.; Fu, B.X.; Plagge, A.; Morgan, S.E. POSS-nylon 6 nanocomposites: Influence of POSS structure on surface and bulk properties. J. Polym. Sci. Part B Polym. Phys. 2009, 47, 1088–1102. [Google Scholar] [CrossRef]
  22. Andrade, R.J.; Weinrich, Z.N.; Ferreira, C.I.; Schiraldi, D.A.; Maia, J.M. Optimization of melt blending process of nylon 6-POSS: Improving mechanical properties of spun fibers. Polym. Eng. Sci. 2015, 55, 1580–1588. [Google Scholar] [CrossRef]
  23. Fina, A.; Monticelli, O.; Camino, G. POSS-based hybrids by melt/reactive blending. J. Mater. Chem. 2010, 20, 9297–9305. [Google Scholar] [CrossRef]
  24. Sirin, H.; Kodal, M.; Ozkoc, G. The influence of POSS type on the properties of PLA. Polym. Comp. 2016, 37, 1497–1506. [Google Scholar] [CrossRef]
  25. Zhao, Y.; Schiraldi, D.A. Thermal and mechanical properties of polyhedral oligomeric silsesquioxane (POSS)/polycarbonate composites. Polymer 2005, 46, 11640–11647. [Google Scholar] [CrossRef]
  26. Li, B.; Zhang, Y.; Wang, S.; Ji, J. Effect of POSS on morphology and properties of poly(2,6-dimethyl-1,4-phenylene oxide)/polyamide 6 blends. Eur. Polym. J. 2009, 45, 2202–2210. [Google Scholar] [CrossRef]
  27. Fu, Z.; Wang, H.; Zhao, X.; Horiuchi, S.; Li, Y. Immiscible polymer blends compatibilized with reactive hybrid nanoparticles: Morphologies and properties. Polymer 2017, 132, 353–361. [Google Scholar] [CrossRef]
  28. Jose, S.; Thomas, S.; Lievana, E.; Karger-Kogsis, J. Morphology and mechanical properties of polyamide 12 blends with styrene/ethylene-butylene/styrene rubbers with and without meleation. J. Appl. Polym. Sci. 2005, 95, 1376. [Google Scholar] [CrossRef]
  29. Narathichat, M.; Kummerlowe, C.; Vennemann, N.; Sahakaro, K.; Nakason, C. Influence of epoxide level and reactive blending on properties of epoxidized natural rubber and nylon 12 blends. Adv. Polym. Technol. 2012, 31, 118–129. [Google Scholar] [CrossRef]
  30. Saengthaveep, S.; Jana, S.C.; Magaraphas, R. Correlation of viscosity ratio, morphology, and mechanical properties of polyamide 12/natural rubber blends via reactive compatibilization. J. Polym. Res. 2016, 23, 1–13. [Google Scholar] [CrossRef]
  31. Yu, F.; Huang, H.-X. Simultaneously toughening and reinforcing poly(lactic acid)/thermoplastic polyurethane blend via enhancing interfacial adhesion by hydrophobic silica nanoparticles. Polym. Test. 2015, 45, 107–113. [Google Scholar] [CrossRef]
  32. Thitsartarn, W.; Fan, X.; Sun, Y.; Yeo, J.; Yuan, D.; He, C. Simultaneous enhancement of strength and toughness of epoxy using POSS-rubber core-shell nanoparticles. Comp. Sci. Technol. 2015, 118, 63–71. [Google Scholar] [CrossRef]
  33. Lendlein, A.; Kelch, S. Shape memory polymers. Angew. Chem. Int. Ed. 2002, 41, 2034. [Google Scholar] [CrossRef]
  34. Ratna, D.; Karger-Kocsis, J. Recent advances in shape memory polymers and composites: A review. J. Mater. Sci. 2008, 43, 254–269. [Google Scholar] [CrossRef]
  35. Liu, C.; Mather, P.T. Thermomechanical characterization of blends of poly(vinyl acetate) with semicrystalline polymer for shape memory applications. Proc. Annu. Tech. Conf-SPE 2003, 2, 1962. [Google Scholar]
  36. Zhang, W.; Chen, L.; Zhang, Y. Surprising shape-memory effect of polylactide resulted from toughening by polyamide elastomer. Polymer 2009, 50, 1311–1315. [Google Scholar] [CrossRef]
  37. Campo, C.J.; Mather, P.T. PVDF/PMMA shape memory blends. Polym. Mater. Sci. Eng. 2005, 93, 933. [Google Scholar]
  38. Parhizkar, M.; Reardon, P.J.T.; Knowles, J.C.; Browning, R.J.; Stride, E.; Pedley, R.B.; Grego, T.; Edirisinghe, M. Performance of novel high throughput multi electrospray systems for forming of polymeric micro/nanoparticles. Mater. Des. 2017, 126, 73. [Google Scholar] [CrossRef]
  39. Zhou, Y.; Xi, S.; Huang, Y.; Kong, M.; Yang, Q.; Li, G. Preparation of near-spherical PA12 particles for selective laser sintering via Plateau-Rayleigh instability of molten fibers. Mater. Des. 2020, 190, 108578. [Google Scholar] [CrossRef]
  40. Alenezi, H.; Muhammet, E.C.; Mohan, E. Experimental and theoretical investigation of the fluid behavior during polymeric fiber formation with and without pressure. Appl. Phys. Rev. 2019, 6, 041401. [Google Scholar] [CrossRef]
  41. Mahalingam, S.; Matharu, R.; Homer-Vanniasinkam, S.; Edirisinghe, M. Current methodologies and approaches for the formation of core–sheath polymer fibers for biomedical applications. Appl. Phys. Rev. 2020, 7, 041302. [Google Scholar] [CrossRef]
  42. Mahalingam, S.; Huo, S.; Homer-Vanniasinkam, S.; Edirisinghe, M. Generation of core–sheath polymer nanofibers by pressurised gyration. Polymers 2020, 12, 1709. [Google Scholar] [CrossRef] [PubMed]
Materials 14 00027 g001 550
Figure 1. Chemical structure of glycidylisobutyl polyhedral oligomericsilsesquioxane (G-POSS).
Figure 1. Chemical structure of glycidylisobutyl polyhedral oligomericsilsesquioxane (G-POSS).
Materials 14 00027 g001
Materials 14 00027 g002 550
Figure 2. FE-SEM images of polyamide12 (PA12)/polyolefin elastomer (POE)/G-POSS blends with different G-POSS contents of (a) 0, (b) 1, (c) 3, (d) 5 and (e) 10 phr.
Figure 2. FE-SEM images of polyamide12 (PA12)/polyolefin elastomer (POE)/G-POSS blends with different G-POSS contents of (a) 0, (b) 1, (c) 3, (d) 5 and (e) 10 phr.
Materials 14 00027 g002
Materials 14 00027 g003 550
Figure 3. Variation of dispersed domain size in blend with G-POSS content.
Figure 3. Variation of dispersed domain size in blend with G-POSS content.
Materials 14 00027 g003
Materials 14 00027 g004 550
Figure 4. Stress–strain curves of samples.
Figure 4. Stress–strain curves of samples.
Materials 14 00027 g004
Materials 14 00027 g005 550
Figure 5. Variation of (a) storage modulus; (b) tan δ with temperature of samples.
Figure 5. Variation of (a) storage modulus; (b) tan δ with temperature of samples.
Materials 14 00027 g005
Materials 14 00027 g006 550
Figure 6. Thermally triggered shape memory procedure of samples with different POSS contents.
Figure 6. Thermally triggered shape memory procedure of samples with different POSS contents.
Materials 14 00027 g006
Table
Table 1. Tensile properties and Izod impact strength of samples.
Table 1. Tensile properties and Izod impact strength of samples.
G-POSS
Contents
(phr)		Young’s
Modulus
(MPa)		Tensile
Strength
(MPa)		Elongation
at Break
(%)		Toughness
(MPa)		Izod Impact Strength
(kJ/m2)
05 ± 0.218 ± 0.350 ± 2853 ± 4030 ± 0.3
17 ± 0.320 ± 0.366 ± 31216 ± 5033 ± 0.3
39 ± 0.320 ± 0.368 ± 31245 ± 5034 ± 0.4
510 ± 0.322 ± 0.371 ± 31323 ± 6035 ± 0.4
1010 ± 0.323 ± 0.463 ± 31365 ± 6036 ± 0.3
Table
Table 2. Glass transition temperature of samples.
Table 2. Glass transition temperature of samples.
G-POSS Contents (phr)Tg of POE (°C)Tg of PA12 (°C)
0−53.947.1
1−56.145.9
3−56.345.8
5−54.343.9
10−56.241.8
Table
Table 3. Shape memory properties of PA12/POE/G-POSS blend with different POSS contents.
Table 3. Shape memory properties of PA12/POE/G-POSS blend with different POSS contents.
G-POSS Contents (phr)Shape Fixity Ratio Rf (%)Shape Recovery Ratio Rr (%)
097.447.5
195.975.8
395.585.7
595.892.6
1095.295.9
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Lee, D.-H.; Chang, Y.-W.; Jang, K.-S. Morphology, Mechanical Properties and Shape Memory Effects of Polyamide12/Polyolefin Elastomer Blends Compatibilized by Glycidylisobutyl POSS. Materials 2021, 14, 27. https://doi.org/10.3390/ma14010027

AMA Style

Lee D-H, Chang Y-W, Jang K-S. Morphology, Mechanical Properties and Shape Memory Effects of Polyamide12/Polyolefin Elastomer Blends Compatibilized by Glycidylisobutyl POSS. Materials. 2021; 14(1):27. https://doi.org/10.3390/ma14010027

Chicago/Turabian Style

Lee, Dong-Hun, Young-Wook Chang, and Keon-Soo Jang. 2021. "Morphology, Mechanical Properties and Shape Memory Effects of Polyamide12/Polyolefin Elastomer Blends Compatibilized by Glycidylisobutyl POSS" Materials 14, no. 1: 27. https://doi.org/10.3390/ma14010027

APA Style

Lee, D. -H., Chang, Y. -W., & Jang, K. -S. (2021). Morphology, Mechanical Properties and Shape Memory Effects of Polyamide12/Polyolefin Elastomer Blends Compatibilized by Glycidylisobutyl POSS. Materials, 14(1), 27. https://doi.org/10.3390/ma14010027

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