Dispersion of alkylated graphene in organic solvents and its potential for lubrication applications

石墨烯 材料科学 烷基 色散(光学) 分散稳定性 烷基化 十六烷 化学工程 碳氢化合物 有机化学 化学 纳米技术 纳米颗粒 催化作用 工程类 物理 光学
作者
Shivani Choudhary,Harshal P. Mungse,Om P. Khatri
出处
期刊:Journal of Materials Chemistry [Royal Society of Chemistry]
卷期号:22 (39): 21032-21032 被引量:246
标识
DOI:10.1039/c2jm34741e
摘要

We report on the preparation of alkylated graphenes on a large scale followed by their dispersion in organic solvents. The alkylated graphenes with variable alkyl chain lengths (Cn = 8, 12, 18) are prepared by coupling of alkylamine with carboxylic groups of graphene oxide (GrO). The FTIR, UV-Visible, and TGA results reveal that, during alkylation, the oxygen functionalities of GrO are reduced significantly and the average size of the sp2 carbon domain increased, which is further supported by Raman characteristics. It is observed that the dispersibility of alkylated graphene in hydrocarbon solvents increases on increasing the chain length of (a) hydrocarbon solvents used for the dispersion and (b) alkyl groups attached to the graphene. The van der Waals interaction between methylene units associated with alkylated graphenes and hydrocarbon solvents plays a crucial role in determining their dispersion characteristics, and such an interaction increases with increasing methylene units. Octadecylamine functionalized graphene (ODA-Gr) dispersion in hexadecane is found to have long-term dispersion stability due to its high degree of cohesive interaction. The lubrication characteristics of hexadecane containing ODA-Gr were probed by evaluating its friction and wear properties. The results reveal that hexadecane doped with an optimized dose of 0.06 mg mL−1 ODA-Gr reduced friction and wear by 26% and 9%, respectively, compared to hexadecane. The lubricity enhancement could be attributed to uninterrupted supplies of graphene nanosheets under the rubbing surfaces, where these nanosheets prevent direct contact between the rubbing surfaces, providing low resistance to shear.
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