Prospects for reducing energy consumption in zinc oxide technology

The heat-technological scheme for the production of zinc oxide from metallic zinc is considered. It is shown that the thermal efficiency factor of the existing industrial process is very low and is equal to 5%. The technological process thermodynamics analysis showed that the zinc vapor combustion exothermic reaction heat is sufficient to provide heat for all endothermic technology stages. The conditions and design of the installation, which make it possible to use this heat for all stages of the technological process, are considered. This provides an increase efficiency factor up to 44%.

Enhanced Performance of Zn/Br Flow Battery Using N-Methyl-N-Propylmorpholinium Bromide as Complexing Agent

Redox flow batteries (RFB) are one of the most interesting technologies in the field of energy storage, since they allow the decoupling of power and capacity. Zinc–bromine flow batteries (ZBFB) are a type of hybrid RFB, as the capacity depends on the effective area of the negative electrode (anode), on which metallic zinc is deposited during the charging process. Gaseous bromine is generated at the positive electrode (cathode) during the charging process, so the use of bromine complexing agents (BCA) is very important. These BCAs are quaternary amines capable of complexation with bromine and generating an organic phase, immiscible with the aqueous electrolyte. One of the most commonly used BCAs in RFB technology is 4-methylethylmorpholinium bromide (MEM-Br). In this work, an alternative quaternary amine 4-methylpropylmorpholinium bromide (MPM-Br) was studied. MPM-Br was integrated into the electrolyte, and 200 charge–discharge cycles were performed on the resulting ZBFBs. The obtained results were compared with those when MEM-Br was used, and it was observed that the electrolyte with MPM-Br displays a higher resistance in voltage and higher energy efficiency, making it a promising alternative to MEM-Br.

Synthesis of Metallic Zinc Nanoparticles by Reduction of Zinc Ions in Protonic Solvent

Simple and low environmental impact methods for producing chemically-stable nanoparticles of metallic zinc (Zn) are asked to be developed, because metallic Zn nanoparticles are easily oxidized in air, and organic solvents, which can be used for the fabrication of metallic Zn particles, give a great environmental impact. The present work focuses on the chemical reaction in protonic solvents containing aqueous solvents, of which the use will give a smaller environmental load, and proposes a method for producing metallic Zn nanoparticles by reduction of Zn ions in the protonic solvent. Two kinds of hydrophilic solvents were examined: water and ethylene glycol (EG). The use of water and EG as the solvents produced Zn oxide. Though the addition of aluminum salt to EG also produced Zn oxide, the crystallinity of Zn oxide was lower than that for with no addition of aluminum salt. In the case of the aluminum salt addition, nanoparticles with a size of 27. 5±13.3 nm were fabricated, and not only bonds of Zn-O-Zn and Zn-OH but also a bond of Zn-Zn were confirmed to be formed, which indicated the production of low crystallinity metallic Zn nanoparticles.

Indoor and Outdoor Performance Study of Metallic Zinc Particles in Black Paint to Improve Solar Absorption for Solar Still Application

In this study, the effects of metallic zinc (Zn) particles were studied to increase surface temperature on a solar-still absorber, which is a major component of increased production. Various concentrations of Zn particles were mixed in black paint and applied to the absorber plate. SEM and XRD were used to examine and confirm the surface morphology and phase identification of as-received powder. UV-Vis spectroscopy was used to examine light-absorption properties. Finally, extensive indoor testing (using an improvised solar emulator) and outdoor testing were conducted to optimize the concentration. The specimens containing 10 wt% Zn in black paint showed the highest increase in temperature, i.e., 103.53 °C in indoor conditions at 1000 W/m2 irradiation, which is 59.17% higher than a bare aluminum plate and 17.57% higher than an only black-paint-coated aluminum plate. On the other hand, specimens containing 10 wt% Zn reached just 87.53 °C, compared to 80.00 °C for an only black-paint-coated aluminum plate and 60.62 °C for bare aluminum.

2,2-difluorovinyl benzoates for diverse synthesis of gem-difluoroenol ethers by Ni-catalyzed cross-coupling reactions

Abstractgem-Difluoroalkene is a bioisostere of carbonyl group for improving bioavailability of drug candidates. Herein we develop structurally diverse 2,2-difluorovinyl benzoates (BzO-DFs) as versatile building blocks for modular synthesis of gem-difluoroenol ethers (44 examples) and gem-difluoroalkenes (2 examples) by Ni-catalyzed cross coupling reactions. Diverse BzO-DFs derivatives bearing sensitive functional groups (e.g., C = C, TMS, strained carbocycles) are readily prepared from their bromodifluoroacetates and bromodifluoroketones precursors using metallic zinc as reductant. With Ni(COD)2 and dppf [1,1’-bis(diphenylphosphino)ferrocene] as catalyst, reactions of BzO-DFs with arylboronic acids and arylmagnesium/alkylzinc reagents afforded the desired gem-difluoroenol ethers and gem-difluoroalkenes in good yields. The Ni-catalyzed coupling reactions features highly regioselective C(vinyl)–O(benzoate) bond activation of the BzO-DFs. Results from control experiments and DFT calculations are consistent with a mechanism involving initial oxidative addition of the BzO-DFs by the Ni(0) complex. By virtue of diversity of the BzO-DFs and excellent functional group tolerance, this method is amenable to late-stage functionalization of multifunctionalized bioactive molecules.