Preparation and properties of a self-crosslinking styrene acrylic emulsion using amino-functional graphene oxide as a crosslinking agent and anti-corrosion filler

Bio-nanocomposite hydrogels based on sodium alginate (SA) as polymer matrix and graphene oxide (GO) nanosheets with zinc as crosslinking agent were synthesized with the aim of incorporating the intrinsic properties of their constituents (bioactivity and antimicrobial activity). Thus, stable and highly interconnected networks were obtained from GO nanosheets dispersed in SA matrices through interactions with low amounts of zinc. The GO nanosheets were successfully incorporated into the alginate matrix in the form of a complex nano-network involving different interactions: Bonds between alginate chains induced by Zn ions (egg box structure), interactions between GO nanosheets through Zn ions and hydrogen bonds between alginate chains, and GO nanosheets. The molecular interactions and morphology were confirmed by Fourier-transform infrared spectroscopy and transmission electron microscopy. The composite’s structural organization showed enhanced thermal stability. The glass transition temperature shifted to a higher temperature due to the reduced mobility induced by additional crosslinking bonds after incorporating the GO nanosheets and Zn into the polymer matrix. Finally, the dielectric behavior revealed that charge carrier mobility was hampered by the compact structure of the nanonetwork, which reduced conductivity. The combined properties of these nanocomposite hydrogels make them attractive biomaterials in the field of regenerative medicine and wound care since both surface bioactivity and antibacterial behavior are two critical factors involved in the success of a biomaterial.

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Achieving high-performance epoxy nanocomposites with trifunctional poly(oxypropylene)amines functionalized graphene oxide

High Performance Polymers ◽

10.1177/0954008319832353 ◽

2019 ◽

Vol 31 (5) ◽

pp. 557-569 ◽

Cited By ~ 3

Author(s):

Tong Sun ◽

Huawei Zou ◽

Ya Zhou ◽

Rui Li ◽

Mei Liang ◽

...

Keyword(s):

Mechanical Properties ◽

Graphene Oxide ◽

High Performance ◽

Flexural Modulus ◽

Covalent Bonds ◽

Spectra Analysis ◽

Functionalized Graphene Oxide ◽

Ep Matrix ◽

Functional Graphene Oxide ◽

The Relationship

In this article, two types of functional graphene oxide (GO) with amine-rich surface were synthesized through chemically grafting two different molecular chain length trifunctional poly(oxypropylene)amines T5000 and T403, which were named as T5000-GO and T403-GO, respectively. The functionalized GO was then added to epoxy (EP) resin. Fourier transform infrared spectra analysis confirmed successful chemical functionalization on GO. Both T403-GO and T5000-GO were tightly embedded in the EP, because the amine-rich surface of functionalized-GO could form covalent bonds with the EP matrix, thereby contributing to the enhancement of mechanical properties. Particularly, T5000-GO, which has longer grafting molecule chains, achieved better compatibility and dispersibility in the EP matrix, resulting in a better reinforcing efficiency in mechanical properties. For example, the T5000-GO/EP composites showed an incremental enhancement in tensile strength with increasing filler concentrations, whereas their T403-GO/EP counterparts failed to follow the same trend. Meanwhile, the T5000-GO/EP composites with only 0.1-wt% T5000-GO achieved a prominent increase in flexural strength (approximately 50%) and flexural modulus (approximately 26.8%), which were higher than those of T403-GO-filled counterparts. This work indicated that the compatibility and interphase between GO and EP could be designed by manipulating the length of grafting molecule chains, thereby providing a better understanding of the relationship between the structure and mechanical properties of the graphene/EP nanocomposites.

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