A nonionic surfactant, namely long-chain alkylbenzenemethanol polyoxyethylene ether (RBMEO
n), 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 RBMEO
n 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 (NPEO
10) and fatty alcohol ethoxylates (AEO
9). It is found that the surface activity of RBMEO
10 is somewhat superior to NPEO
10 and AEO
9.
Keywords: Alkylbenzenemethanol polyether, synthesis, surface activity