Intermolecular interactions in mixed dye systems and the effects on dye wastewater treatment processes.

Dye wastewater discharge is a critical concern across textiles, paper, cosmetics, and other industries. This study explores the impact of dye-dye interactions on chemical coagulation and ultrafiltration process. Using basic and reactive dyes, representing cationic and anionic compounds, the intricate interplay between these dyes was examined through spectroscopic analysis. Remarkably, interactions between dyes of opposite charges exhibited significant effects on both techniques. Electrostatic attractions played a key role. Positive coagulant hydrolysates selectively attracted negative dyes, while negatively charged membranes effectively captured positive dyes. Combining dyes with opposite charges resulted in enhanced removal efficiency, addressing challenging dyes collectively. This discovery offers a novel approach to improving dye removal, utilizing opposite-charged dye mixtures can tackle stubborn dyes unmanageable by conventional methods.

Fully Physically Crosslinked Conductive Hydrogel with Ultrastretchability, Transparency, and Self-Healing Properties for Strain Sensors.

Currently, conductive hydrogels have received great attention as flexible strain sensors. However, the preparation of such sensors with integrated stretchability, transparency, and self-healing properties into one gel through a simple method still remains a huge challenge. Here, a fully physically crosslinked double network hydrogel was developed based on poly(hydroxyethyl acrylamide) (PHEAA) and κ-carrageenan (Car). The driving forces for physical gelation were hydrogen bonds, ion bonding, and electrostatic interactions. The resultant PHEAA-Car hydrogel displayed stretchability (1145%) and optical transparency (92%). Meanwhile, the PHEAA-Car hydrogel exhibited a self-healing property at 25 °C. Additionally, the PHEAA-Car hydrogel-based strain sensor could monitor different joint movements. Based on the above functions, the PHEAA-Car hydrogel can be applied in flexible strain sensors.

Efficiently Removing Heavy Metals from High-Salinity Wastewater via Ionic Liquid-Based Aqueous Biphasic Systems.

For the separation of metal ions, ionic liquid-based aqueous biphasic systems (IL-ABSs) offer a promising alternative to solvent extraction. However, the incorporation of an extensive quantity of inorganic salts restricts their practical application. Because heavy metal wastewater often contains high concentrations of inorganic salts, it offers good prospects for the application of IL-ABSs in the separation of heavy metals. In this work, an IL-ABS was formed by tributyltetradecylphosphonium chloride ([P44414]Cl), and simulated high-salinity wastewater (NaCl and Na2SO4 as the main inorganic salts) was used for the separation of heavy metals. The phase diagram results indicated that the formation of a two-phase system required a relatively high salt concentration. The extraction process followed the mechanism of anion exchange; thus, heavy metals such as zinc and cadmium that formed complexes with chloride ions could be effectively extracted (extraction rate >99.5%) with a very fast rate (extraction time <1 min) at a wide pH range (pH = 2-7). After extraction, the metals could be stripped well (stripping rate >99.5%) after contact with the NaOH solution. This research provided a new approach for treating heavy metals in high-salinity effluents, which has the advantages of IL-ABS and avoids the disadvantages of adding large amounts of inorganic salts at the same time.

Dual Lewis Base Functionalization of Ionic Liquids for Highly Efficient and Selective Capture of H2 S.

Three dual Lewis base functionalized ionic liquids (DLB-ILs) tethered with both carboxyl and tertiary amine groups on their anions were designed for highly efficient and selective absorption of H2 S. It was found that the DLB-ILs could reversibly absorb 0.39-0.84 mol of H2 S per mole of IL at 1 bar and 60 °C, which is significantly higher than that of other ILs. On the contrary, the CO2 absorption in this class of DLB-ILs was shown to be quite limited relative to H2 S owing to the coupling effect of the two Lewis base groups. It is the dual Lewis base functionalization that enables the significantly high values calculated for the ideal absorption selectivity for H2 S/CO2 , that is, 13-26 at 1 bar and 29-70 at 0.1 bar (60 °C). The selectivity even goes up to >100 at low pressures and high temperatures. It was further illustrated from DFT calculations and spectroscopy studies that the cooperation interaction of carboxyl⋅⋅⋅H2 S⋅⋅⋅amine and the reduced binding with CO2 were the major contributions to the high H2 S absorption capacity and H2 S/CO2 selectivity.