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Ultrahigh molecular weight polyethylene (UHMWPE) is an excellent material with high performance, but it is very difficult to covalently introduce functional groups on its surface owing to its inherently inert structure, which constrains its further application. In this study, vinyl triethoxysilane (VTEOS) containing hydrolysable alkoxyl groups was in situ grafted on UHMWPE by air plasma treatment. The plasma treatment conditions for VTEOS grafting were optimized. The structure of the modified UHMWPE was characterized with FTIR and XPS. The relatively high VTEOS content was obtained when the treating conditions were about 20 W, 125 Pa for 10 min. And FTIR results showed that the grafted structure on the surface was stable for long time duration in the ambient environment. After the treatment, the roughness of the surface increased and the water contact angle of the modified sample dropped to 47.5° from 92.8° of the unmodified one. TGA and XRD results indicated that plasma treatment would not change the bulk structure of UHMWPE greatly. Cell culture experiments showed that fibroblasts on the modified samples had notably high viability and proliferation rate with good adhesion shape. Hence, it might be an effective method to improve the surface properties of UHMWPE for biomedical applications by plasma-induced in-situ grafting with VTEOS. © 2017 Wiley Periodicals, Inc. J Biomed Mater Res Part A: 106A: 321-332, 2018. [ABSTRACT FROM AUTHOR]

The fabrication of advanced graphene-based nanocomposites with high-performance polymers requires covalent modification of graphene with aromatic macromolecules. Herein, C-N coupling reactions between fluorinated graphene (FG) and aromatic polyamides containing the benzimidazole moiety are successfully achieved. The optimized conditions are presented based on the nucleophilic behavior of the C-N coupling reaction on graphene. Different from the C-N coupling reaction between two small aromatic molecules, the conformation of grafted aromatic polyamide after reaction changes from torsional to paralleled alignment on graphene with the molecular length increment. Non-covalent interactions between graphene and aromatic polyamides result in this conformational change owing to the extended π systems of graphene and aromatic polyamides, and the synergistic effect of covalent and non-covalent interactions is put forward. As a consequence, graphene dispersibility is greatly enhanced in the solution of aromatic polyamide., (© 2019 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim.)