In this study, imidazole derivative-based new ionic liquids were investigated as corrosion inhibitors. These new ionic liquids (ILs) are 1,3-dipropyl-2-(2-propoxyphenyl)-4,5-diphenylimidazole iodide (IL1) and 1,3-dibutyl-2-(2-butoxyphenyl)-4,5-diphenylimidazole iodide (IL2). The corrosion inhibition effects of two new ILs were observed on carbon steel in brackish water media (1% NaCl solution). Carbon steel coupons were exposed to 1% NaCl solution with various concentrations of ILs. Corrosion inhibition effects were tested by the electrochemical impedance spectroscopy (EIS) method and the Tafel method at various temperatures ranging from 25 °C to 55 °C. The results showed that ILs have potential as corrosion inhibitors and the adsorption mechanisms of IL1 and IL2 on carbon steel surfaces were also determined, which followed the Langmuir adsorption isotherm model. Acquisition of ∆G_ads values of IL1 and IL2 were −35.04 and −34.04 kJ/mol, respectively. The thermodynamic data of the ILs show that semi-chemical and or physical adsorptions occurred on carbon steel surfaces.

The separation process between 5-hydroxymethylfurfural (HMF) and trace glucose in glucose conversion is important in the biphasic system (aqueous–organic phase), due to the partial solubility property of HMF in water. In addition, the yield of HMF via the dehydration reaction of glucose in water is low (under 50%) with the use of Brønsted acid as a catalyst. Therefore, this study was conducted to optimize the production and separation of products by using a new hydrophobic ionic liquid (IL), which is more selective than water. The new IL (1,3-dibutyl-2-(2-butoxyphenyl)-4,5-diphenyl imidazolium iodide) [DBDIm]I was used as a solvent and was optimized for the dehydration reaction of glucose to make a more selective separation of HMF, levulinic acid (LA), and formic acid (FA). [DBDIm]I showed high performance as a solvent for glucose conversion at 100 °C for 120 min, with a yield of 82.2% HMF, 14.9% LA, and 2.9% FA in the presence of sulfuric acid as the Brønsted acid catalyst.

Trade-off issue and membrane fouling remain two major issues in the utilization of membrane technology for the water treatment due to reduced membrane permeability and lifetime. In our study, we employed 3-aminopropyltriethoxysilane modified bentonite (BNTAPS) as an anti-fouling modifier to prepare polyvinylidene fluoride (PVDF)-based membranes via the phase inversion method. The effects of BNTAPS concentration on the physical, mechanical, morphological, and filtration performance of the hybrid membranes have been investigated. It was found that the addition of BNTAPS improved the hydrophilicity of the membrane revealed by the decreased water contact angle. Consequently, the pure water flux of PVDF membrane containing 0.5% BNTAPS (PVDF/BNTAPS0.5%) increased to 35.5 L m^-2 h^-1. Moreover, the PVDF/BNTAPS membrane showed a smaller pore diameter and porosity compared to pristine PVDF. The membrane performance evaluation was carried out using cationic and anionic dyes, i.e., methylene blue (MB) and acid yellow (AY17), respectively. Our study revealed that the rejection of each dye was slightly increased for the PVDF/BNTAPS0.5%. However, the flux recovery rate of the PVDF/BNTAPS membrane significantly improved, which directly prolonged the membrane lifetime.

Immobilization of enzymes is one of the most promising methods in enzyme performance enhancement, including stability, recovery, and reusability. However, investigation of suitable solid support in enzyme immobilization is still a scientific challenge. Polyethersulfone (PES) and aminated PES (PES–NH₂) were successfully synthesized as novel materials for immobilization. Membranes with various pore sizes (from 10–600 nm) based on synthesized PES and PES–NH₂ polymers were successfully fabricated to be applied as bioreactors to increase the immobilized lipase performances. The influence of pore sizes, concentration of additives, and the functional groups that are attached on the PES backbone on enzyme loading and enzyme activity was studied. The largest enzyme loading was obtained by Mucor miehei lipase immobilized onto a PES–NH₂ membrane composed of 10% of PES–NH₂, 8% of dibutyl phthalate (DBP), and 5% of polyethylene glycol (PEG) (872.62 µg/cm²). Hydrolytic activity of the immobilized lipases indicated that the activities of biocatalysts are not significantly decreased by immobilization. From the reusability test, the lipase immobilized onto PES–NH₂ showed a better constancy than the lipase immobilized onto PES (the percent recovery of the activity of the lipases immobilized onto PES–NH₂ and PES are 97.16% and 95.37%, respectively), which indicates that this novel material has the potential to be developed as a bioreactor for enzymatic reactions.

Given the desirable outcomes to organic synthesis afforded by the use of ionic liquids1–4 there is a need for the development of more efficient techniques for their preparation. The microwave-assis...