Table 2.
Functionalizations of CNTs and MLG.
| entry | process | description | advantages | ref. |
| chemical or covalent functionalization | ||||
| 1 | organic hydrazine functionalization | reaction with organic hydrazine in an aqueous surfactant solution under argon | improved purity, solubility, and physical properties | [36,117] |
| 2 | silane functionalization | silanization in a (3-glycidoxypropyl)trimethoxysilane solution at 60–65 °C for about 6 h | Functional groups attached at the defect sites can undergo further chemical reactions | [53] |
| 3 | strong acids | treatment of MLG and CNTs with a mixture of sulfuric acid and nitric acid causes functionalization of MLG and sidewalls of CNTs | Oxygenated side groups exert electrostatic repulsive forces causing exfoliation. | [40] |
| 4 | oxidation | surface oxidization by heat treatment in oxygen or air, plasma treatment, chemical treatment, and ozone treatment | decrease of contact angle | [55,58] |
| physical or non-covalent functionalization | ||||
| 5 | surfactant functionalization | Surfactants are physically absorbed on the surface of the filler. | lowers surface tension of filler, avoids filler segregation | [40] |
| 6 | endothermal | atoms or molecules are inserted inside the CNTs by capillary action through defect sites | can significantly improve thermal and electrical conductivities | [40] |