Surfactant Monolayer Bending Elasticity in Lipase Containing Bicontinuous Microemulsions

Lipase-catalyzed reactions offer many advantages among which a high degree of selectivity combined with the possibility to convert even non-natural substrates are of particular interest. A major drawback in the applicability of lipases in the conversion of synthetically interesting, non-natural substrates is the substantial insolubility of such substrates in water. The conversion of substrates, natural or non-natural, by lipases generally involves the presence of a water–oil interface. In the present paper, we exploit the fact that the presence of lipases, in particular the lipase from Candida antarctica B (CalB), changes the bending elastic properties of a surfactant monolayer in a bicontinuous microemulsion consisting of D2O/NaCl -n-(d)-octane-pentaethylene glycol monodecyl ether (C10E5) in a similar manner as previously observed for amphiphilic block-copolymers. To determine the bending elastic constant, we have used two approaches, small angle neutron scattering (SANS) and neutron spin echo (NSE) spectroscopy. The time-averaged structure from SANS showed a slight decrease in bending elasticity, while on nanosecond time scales as probed with NSE, a stiffening has been observed, which was attributed to adsorption/desorption mechanisms of CalB at the surfactant monolayer. The results allow to derive further information on the influence of CalB on the composition and bending elasticity of the surfactant monolayer itself as well as the underlying adsorption/desorption mechanism.

Pt-Co3O4 Superstructures by One-Pot Reduction/Precipitation in Bicontinuous Microemulsion for Electrocatalytic Oxygen Evolution Reaction

Bicontinuous microemulsions (BCME) were used to synthesize hierarchical superstructures (HSs) of Pt-Co3O4 by reduction/precipitation. BCMEs possess water and oil nanochannels, and therefore, both hydrophilic and lipophilic precursors can be used. Thus, PtAq-CoAq, PtAq-CoOi, PtOi-CoAq and PtOi-CoOi were prepared (where Aq and Oi stand for the precursor present in aqueous or oily phase, respectively). The characterization of the Pt-Co3O4-HS confirmed the formation of metallic Pt and Co3O4 whose composition and morphology are controlled by the initial pH and precursor combination, determining the presence of the reducing/precipitant species in the reaction media. The electrocatalytic activity of the Pt-Co3O4-HSs for oxygen evolution reaction (OER) was investigated using linear sweep voltammetry in 0.1 M KOH and compared with Pt-HS. The lowest onset overpotentials for Pt-Co3O4-Hs were achieved with PtOi-CoOi (1.46 V vs. RHE), while the lowest overpotential at a current density of 10 mA cm−2 (η10) was obtained for the PtAq-CoAq (381 mV). Tafel slopes were 102, 89, 157 and 92 mV dec−1, for PtAq-CoAq, PtAq-CoOi, PtOi-CoAq and PtOi-CoOi, respectively. The Pt-Co3O4-HSs showed a better performance than Pt-HS. Our work shows that the properties and performance of metal–metal oxide HSs obtained in BCMEs depend on the phases in which the precursors are present.

Viscosity Modification of Polymerizable Bicontinuous Microemulsion by Controlled Radical Polymerization for Membrane Coating Applications

Membrane modification is becoming ever more relevant for mitigating fouling phenomena within wastewater treatment applications. Past research included a novel low-fouling coating using polymerizable bicontinuous microemulsion (PBM) induced by UV-LED polymerization. This additional cover layer deteriorated the filtration capacity significantly, potentially due to the observed high pore intrusion of the liquid PBM prior to the casting process. Therefore, this work addressed an innovative experimental protocol for controlling the viscosity of polymerizable bicontinuous microemulsions (PBM) before casting on commercial ultrafiltration (UF) membranes. Prior to the coating procedure, the PBM viscosity modulation was carried out by controlled radical polymerization (CRP). The regulation was conducted by introducing the radical inhibitor 2,2,6,6-tetramethylpiperidine 1-oxyl after a certain time (CRP time). The ensuing controlled radical polymerized PBM (CRP-PBM) showed a higher viscosity than the original unpolymerized PBM, as confirmed by rheological measurements. Nevertheless, the resulting CRP-PBM-cast membranes had a lower permeability in water filtration experiments despite a higher viscosity and potentially lower pore intrusion. This result is due to different polymeric structures of the differently polymerized PBM, as confirmed by solid-state nuclear magnetic resonance (NMR) investigations. The findings can be useful for future developments in the membrane science field for production of specific membrane-coating layers for diverse applications.