Understanding the Hydration Thermodynamics of Cationic Quaternary Ammonium and Charge-Neutral Amine Surfactants

Abstract

Aqueous solubility and interfacial adsorption of surfactants are important for numerous applications. Using molecular dynamics, we have studied the effect of the type of the polar headgroup (cationic quaternary ammonium and charge-neutral amine) and length of the alkyl tail on the hydration free energy of surfactants in infinite dilution. In addition, we have studied the effect of replacing the terminal methyl group of the alkyl tail with a more polar hydroxyl group on the hydration free energy. Quaternary ammonium surfactants have strongly favorable hydration free energies, whereas charge-neutral amine surfactants have unfavorable hydration free energies. The contribution of the quaternary ammonium group in reducing the hydration free energy is estimated to be as large as ∼63 k B T and that of the charge-neutral amine group to be 3 k B T. Both surfactants and their corresponding alkanes have minima in the free energy at the air−water interface. The quaternary ammonium group contributes to a 6 k B T decrease in the free energy of transfer from air−water interface to bulk aqueous phase (termed henceforth as interface transfer free energy). The amine group, on the other hand, has a net zero interface transfer free energy. The interface transfer free energies of surfactants are both enthalpically and entropically unfavorable. The enthalpic penalty is attributed to the loss of water−water interactions. Interestingly, surfactant molecules gain entropy upon their transfer from the air−water interface to the aqueous phase, but this increase is more than compensated by the loss in the entropy of water molecules, presumably due to the ordering of water molecules around the surfactants. Replacing the terminal methyl group of the alkyl tail with a hydroxyl group in quat surfactants reduces their hydration free energy by 10 k B T, thus making them more soluble in water. Attaching a hydroxyl group to the alkyl tail also inhibits their micelle forming tendency in the bulk aqueous phase. Overall, this work reveals how tuning the molecular characteristics of surfactants can help to achieve the desirable aqueous solubility, interfacial properties, and micellization tendency of surfactants.

Recent Trends and Progress in Corrosion Inhibitors and Electrochemical Evaluation

“…In the presence of O 2 , CO 2 inhibitors exhibit a significant decrease in inhibition performance. According to Singh et al [33] in the presence of 100 ppb O 2 at 40 • C (1 bar CO 2 , pH 5.5), the inhibitory efficacies of all imidazoline-based, quaternary ammonium-based, and amine-based processes were significantly reduced because the N atoms interact with oxygen and the inhibitor volatilizes from the metal surface. According to Wang et al [34], in a coexisting O 2 and CO 2 environment, the corrosion prevention efficacy of 8 × 10 −5 mol L −1 amides was only 80.3%, whereas it was 98.3% in a CO 2 -saturated solution.…”