Redox Flow Capacitive Deionization in a Mixed Electrode Solvent of Water and Ethanol

In the redox flow electrode capacitive deionization (FCDI), the solubility of redox electrolyte and flowability of carbon slurry have great influence on the salt removal rate and energy consumption. In this work, a mixed solvent electrolyte is proposed in FCDI, which consists of iodide/triiodide redox couples and carbon slurry in the mixed solvent of water and ethanol (1:1). At the current density of 5 mA cm-2, the salt removal rate can reach up to 2.72 μg cm-2 s-1 in a mixed solvent, which is much higher than 1.74 μg cm-2 s-1 in aqueous solution and 2.37 μg cm-2 s-1 in the ethanol solution. This may be owing to the fast transport of ions during redox reaction in organic solvent and the excellent flowability of carbon slurry in the aqueous condition, which can provide more reaction sites for iodide/triiodide redox reaction and faster electron transportation. This unique FCDI with organic and aqueous mixed solvent electrolyte will provide a new perspective for the development of redox flow electrochemical desalination.

Synthesis of Novel (S)-3-(1-Aminoethyl)-8-pyrimidinyl-2-phenylisoquinolin-1(2H)-ones by Suzuki–Miyaura Coupling and Their Cell Toxicity Activities

A series of (S)-3-(1-aminoethyl)-8-pyrimidinyl-2-phenylisoquinoline-1(2H)-ones 3a–3k was synthesized in 40–98% yield through Suzuki–Miyaura coupling using Pd(PPh3)2Cl2, Sphos, and K2CO3 in THF/H2O mixed solvent. All newly synthesized compounds were evaluated for cell viability (IC50) against MDA-MB-231, HeLa, and HepG2 cells. The antitumor activities of 3a–3k were improved when various pyrimidine motifs were introduced at position C-8 of the isoquinolinone ring.

Neutralization of solvent vapors of brand 650 by the adsorption‑catalytic method

The purpose of this work is to study the process of neutralization of vapors of a mixed solvent of the brand 650 by the adsorption‑catalytic method. The essence of the method consists in the concentration of solvent components on the sorbent, thermal desorption followed by periodic flameless catalytic oxidation of accumulated organic substances to carbon dioxide and water. Synthetic zeolite of the NaX brand was used as a sorbent, and a porous material based on foam ceramics of the Al2O3/SiO2 composition with a highly developed modified surface with an active catalytic phase was used as a catalyst. The mixed solvent contains, xylenes, ethylcellosol, n‑butanol. It is shown that the value of the sorption volume of zeolite for each class of the considered compounds is influenced by certain factors: the length and structure of the carbon skeleton, the position of the hydroxyl group (for alcohols and esters), the number of methyl groups in the composition of molecules (for the production of benzene). The conversion rate of the mixed solvent components was 65.4–90.1 %.

Synthesis of Vinylene-Linked Covalent Organic Frameworks by Monomer-Self-Catalyzed Activation of Knoevenagel Condensation

Reticular chemistry on the basis of thermodynamically controlled linking modes and numerous organic building blocks has constituted versatile crystalline frameworks in molecular-level precision. However, vinylene-linked organic frameworks (COFs) are still quite far from flexible tailoring either in their structures or topologies, due to the lack of monomers with sufficient activities. Herein, we established a strategy to synthesize vinylene-linked COFs via Knoevenagel condensation of a tetratopic monomer 2,2’,6,6’-tetramethyl-4,4’-bipyridine (TMBP) with linear aromatic dialdehydes in a mixed solvent of benzoic anhydride and benzoic acid. Mechanism investigation suggested that the condensation was promoted by a pyridine-self-catalyzed benzoylation upon the cleavage of benzoic anhydride solvent molecules. The layered structures of the resultant COFs were highly crystallized into orthorhombic lattice with vertically aligned AA stacking mode, delivering high surface areas up to 1560 m2 g-1. The pi-extended conjugated skeletons comprising para-bipyridyl units and vinylene linkages endow these COFs with substantial semiconducting properties, releasing visible light-stimulated catalytic activity in water-splitting hydrogen evolution with a rate as high as 3300 μmol g-1 h-1.

Mixed Solvents in Multi-Layer Ceramic Capacitors (MLCC) Elec-Tronic Paste and Their Effects on the Properties of Organic Vehicle

The copper end paste used in multilayer ceramic capacitors sintered in nitrogen atmosphere will lead to carbon residue of organic vehicle, which will lead to the reduction of electrode conduc-tivity and high scrap rate. With an attempt to leave no residue in the sintering, the compatibility of solvents and thickeners should be improved because it has an important influence on the hi-erarchical volatilization and carbon residue of organic vehicles. In this work, the volatility of different solvents was compared and several solvents were mixed in a definite proportion to prepare an organic vehicle with polyacrylate resins. The hierarchical volatility and solubility parameters of mixed solvents were adjusted effectively by changing proportions of different components, the thermogravimetric curves of resins and organic vehicles were measured by thermogravimetric analyzer, the effect of solubility parameter on the dissolvability of resins in the solvent and the residual of organic vehicles were studied. Results showed that the hierar-chical volatilization of solvents can be obtained by mixing different solvents; the intrinsic vis-cosity of the organic vehicle is higher and the thermal decomposition residue of polyacrylate resins is lower when the solubility parameters of mixed solvents and polyacrylate resins are closer. The low residual sintering of organic vehicles can be achieved by using the mixed solvent with hierarchical volatility and approximate solubility parameters as resins.