Skip to main content
U.S. flag

An official website of the United States government

Official websites use .gov
A .gov website belongs to an official government organization in the United States.

Secure .gov websites use HTTPS
A lock ( ) or https:// means you’ve safely connected to the .gov website. Share sensitive information only on official, secure websites.

N-Pyrrolidine Functionalized C60-Fullerenes/Epoxy Nanocomposites

Published

Author(s)

Mickey Richardson, Eun S. Park, Jaehyun Kim, Gale A. Holmes

Abstract

A small series of functionalized C60-fullerene/epoxy nanocomposites were prepared, and their respective ultimate tensile strengths were determined. The functionalization route of the fullerenes was performed using the well-known Prato reaction, with modified amino acids, resulting in the formation of N-pyrrolidine rings across the [6,6] junctions. Characterization of the functionalized fullerenes was done using LDI-TOF mass spectrometry. By the type of modified amino acid, the degree of functional group attachment, and the consequent degree of dispersion into the epoxy matrix, the mechanical properties of the nanocomposites were affected. We used a specially blended epoxy matrix by using a lower molecular weight diglycidyl ether, in conjunction with the more recognized diglycidyl ether of bisphenol A (DGEBA). The viscosity of the overall epoxy matrix was decreased by blending the more recognized diglycidyl ether of bisphenol A (DGEBA) with this lower molecular mass diglycidyl ether, thereby allowing easier mixing conditions.
Citation
Journal of Applied Polymer Science
Volume
117

Keywords

C60-Fullerenes, Prato Reaction, Epoxy Nanocomposites

Citation

Richardson, M. , Park, E. , Kim, J. and Holmes, G. (2010), N-Pyrrolidine Functionalized C<sub>60</sub>-Fullerenes/Epoxy Nanocomposites, Journal of Applied Polymer Science, [online], https://tsapps.nist.gov/publication/get_pdf.cfm?pub_id=901134 (Accessed April 20, 2024)
Created March 25, 2010, Updated October 12, 2021