Monday, October 17, 2011
Exhibit Hall B (Minneapolis Convention Center)
A nonionic surfactant, namely long-chain alkylbenzenemethanol polyoxyethylene ether (RBMEOn), was synthesized starting from long-chain alkylbenzene through a three-step route including Friedel-Crafts acylation, reductive reaction and alkoxylation. The structures of reaction intermediates, alkyl benzene ethanone and 4-alkyl-α-methyl-benzenemethanol, were identified by FT-IR and 1H-NMR. The distribution of the EO length in RBMEOn was characterized by ESI-MS. Many important surface active parameters were determined at 35±0.1 oC and were compared with those of structurally-related nonionic surfactants nonyl phenol ethoxylates (NPEO10) and fatty alcohol ethoxylates (AEO9). It is found that the surface activity of RBMEO10 is somewhat superior to NPEO10 and AEO9.
Keywords: Alkylbenzenemethanol polyether, synthesis, surface activity
See more of this Session: Poster Session: Interfacial Phenomena
See more of this Group/Topical: Engineering Sciences and Fundamentals
See more of this Group/Topical: Engineering Sciences and Fundamentals