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.

Adsorption and Desorption Mechanism of Aromatic VOCs onto Porous Carbon Adsorbents for Emission Control and Resource Recovery: Recent Progress and Challenges

As is universally acknowledged, the fast advances in industrialization and urbanization have caused the rapid increase in the emission of aromatic volatile organic compounds (VOCs), which has results in not...

Microwave Desorption Mechanism and Microwave Effect based on SO2 Chemical Dissociation and Mass Transfer of Basic Aluminium Sulfate Desulfurization Rich Liquid

A microwave liquid-phase desorption technique for enhancing mass transfer with chemical dissociation had been proposed for the first time. In this paper, the static desorption system of basic aluminium sulfate...

Novel approach to distinguish between vacuum UV-induced ice photodesorption and photoconversion

Context. In cold regions of the interstellar medium with intense ultraviolet radiation fields, photodesorption has been suggested as a nonthermal desorption mechanism promoting the transition of molecules from the solid state to the gas phase. Laboratory experiments measuring photodesorption rates are crucial in attempting to explain high molecular gas phase abundances of species that are expected to form in the solid state, such as methane, methanol, and acetonitrile, and to aid astrochemical modeling. Due to the convoluted competition between photodesorption and photoconversion, it is far from trivial to derive accurate photodesorption rates. Aims. The aim of this study is to apply a new methodology to discriminate between the two processes. The method has been validated using the well-studied case of CO and extended to CH4, CH3OH, and CH3CN. Methods. Vacuum ultraviolet (VUV; photon energy of 7–10.2 eV) irradiated ices at 20 K are studied, first as a pure CH4, CH3OH, or CH3CN ice and subsequently with an Ar coating on top. The latter is transparent to the VUV photons (wavelength below 200 nm), but it quenches the photodesorption process. Comparing the laser desorption post ionization time-of-flight mass spectrometry of the ices with and without the Ar coating provides information on the different interactions of the VUV photons with the ice. Results. The newly developed experimental technique allowed for a derivation of photodesorption rates for ices at 20 K of: CO (3.1 ± 0.3)×10−3 mol. photon−1, CH4 (3.1 ± 0.5)×10−2 mol. photon−1, and upper limits for CH3OH (< 6 × 10−5 mol. photon−1) and CH3CN (< 7.4 × 10−4 mol. photon−1); in the latter case, no literature values have been reported yet. The newly introduced approach provides more insight into the photodesorption process, in particular, for commonly observed complex organic molecules (COMs). Photoconversion cross sections are presented in the 7–10.2 eV range. The possible role of photodesorption and photoconversion in the formation of interstellar COMs is discussed.

Nickel ion removal from aqueous solutions through the adsorption process: a review

Recently, removal of nickel ions has been gaining a lot of attention because of the negative impact of nickel ions on the environment. The aim of this review paper is to organize the scattered available information on removal of nickel ions from aqueous solutions through the adsorption process. Survey on investigated materials suggests that composite- and polymer-based adsorbents have the most effective capability for nickel adsorption. The composite material class, i.e. CaCO3-maltose, followed by biopolymer-based material showed the highest Ni(II) adsorption capacity of 769.23 and 500 mg/g, respectively. The importance of treatment parameters (i.e. pH, temperature, contact time, and metal ion concentration) is discussed, together with their effect on the underlying physicochemical phenomena, giving particular attention to the adsorption/desorption mechanism. It was ascertained that adsorption of nickel ions is pH dependent and the optimal pH range for adsorption of Ni(II) ions was in range of 6–8. In general, nickel adsorption is an endothermic and spontaneous process that mainly occurs by forming a monolayer on the adsorbent (experimental data are often fitted by Langmuir isotherms and pseudo-second-order kinetics). Regeneration (i.e. desorption) is also reviewed, suggesting that acidic eluents (e.g. HCl and HNO3) allow, in most of the cases, an efficacious spent adsorbent recovery. The percentage use of desorption agents followed the order of acids (77%) > chelators (8.5%) > alkalis (8%) > salts (4.5%) > water (2%). Helpful information about adsorption and desorption of nickel ions from aqueous solutions is provided.