Solvothermal synthesis of graphene oxide and its composites with poly(ε-caprolactone). Issue 40 (7th October 2019)

• Record Type: Journal Article
• Authors: Chin, Seow Jecg; Doherty, Matthew; Vempati, Sesha; Dawson, Paul; Byrne, Cormac; Meenan, Brian J.; Guerra, Valentina; McNally, Tony
• Is Part Of: Nanoscale. Volume 11:Issue 40(2019)
• Page Start: 18672
• Page End: 18682
• Publication Date: 2019-10-07
• Subjects: Nanoscience -- Periodicals; Nanotechnology -- Periodicals; 620.505
• DOI: 10.1039/c9nr04202d
• Languages: English
• ISSNs: 2040-3364

Abstract

Abstract : Graphene oxide (GO) was prepared by a solvothermal synthesis method using sodium and ethanol. Abstract : Graphene oxide (GO) was prepared by a solvothermal synthesis method using sodium and ethanol. A sequence of pyrolysis, washing and purification steps was developed for the total removal of all by-products. The first pyrolysis step is essential to obtain graphitic forms of carbon while a washing and a second pyrolysis step further improved the graphenic structures obtained via the reduction of OH/COOH and C–O groups and the attendant increase in CC bonding (sp 2 hybridization). Two purification processes were employed to remove sodium carbonate (by-product), i.e. vacuum filtration and centrifugation, but the latter produced a more stable GO product, typically with a few-layer ( ca. 3 nm) stack and relatively long platelets (up to ca. 1.3 μm). The functionality of this GO was demonstrated by preparing composites of it with poly(ε-caprolactone) (PCL). Some of the GO was arranged in flower-like domains dispersed in the PCL matrix. The crystalline content of PCL decreased on addition of GO, though the dynamic modulus of PCL increased and an electrical percolation at 0.5 vol% GO was obtained, manifest by a ∼10 4 increase in electrical conductivity (in an overall increase of ∼10 5 achieved at >1 vol%), more than sufficient for anti-static applications.