Numerical Study on the Homogeneous Reactions of Mercury in a 600 MW Coal-Fired Utility Boiler

The homogeneous oxidation of elemental mercury (Hg0) can promote Hg pollution control in coal-fired power plants, while the mechanisms and quantitative contributions of homogeneous reactions in Hg0 oxidation, especially the reactions between Hg and chlorine (Cl), are still unclear. Here, a numerical study on the homogeneous reactions of Hg was conducted within a 600 MW tangentially fired boiler for the first time. A novel Hg sub-model was established by coupling the thermodynamics, reaction kinetics and fluid dynamics. The results showed that the higher Cl content in coal was beneficial to the oxidation of Hg0. The homogeneous reactions of Hg mainly occurred in the vertical flue pass at low temperature. Hg0 was still the dominant Hg-containing species at the boiler exit, and the concentration of mercury chloride (HgCl2) was the highest among the oxidized mercury. When low-Cl coal was fired, the addition of a small amount of chlorine species into the boiler at the burnout area increased the ratio of HgCl2 by over 16 times without causing serious chlorine corrosion problems.

Hypervalent Bromine(III) Compounds: Synthesis, Applications, Prospects

Hypervalent compounds play a prominent role in homogeneous oxidation catalysis. Despite the higher reactivity of the hypervalent bromine compounds when compared to their isoelectronic iodine analogues, the corresponding λ3-bromanes are much less explored. This can be attributed to the discernible lack of convenient strategies for their synthesis. This short review highlights the available methods for the synthesis of various organo-λ3-bromanes, with a major focus on the recent developments and reactivities in the last few years. Additionally, limitations and future prospects of hypervalent bromine chemistry is being discussed.

Influence of Amino Acids and Alcohols on Catalytic Oxidation of Cyclohexane

Conducted experiments and collected data show that use of catalytic systems that contain individual amino acids and industrial catalyst – solution of cobalt naphtenate with cyclohexanone – have certain influence on the process of liquid-phase homogeneous oxidation of cyclohexane. The results of spectral studies of binary catalytic systems based on NC using additives of different nature (alcohols and nitrogen-containing modifiers) allow us to propose structural formulas of catalytic complexes.

Efficient Homogeneous TEMPO-mediated Oxidation of Cellulose in Lithium Bromide Hydrates

An appropriate cellulose-dissolving solvent is critical for the homogeneous oxidation of cellulose using TEMPO (2, 2, 6, 6-tetramethylpiperidine-1-oxyl)-mediated system. Herein, TEMPO/NaClO/NaClO2 system in lithium bromide hydrates (LBHs) was developed for the homogeneous selective-oxidation of cellulose, which was two-stage protocol involving cellulose dissolution and homogeneous oxidation. Specifically, cellulose was firstly dissolved in LiBr⋅3.5H2O and offered the optimal pH (5.6) for the subsequent TEMPO/NaClO/NaClO2 oxidation without precipitation of the cellulose chains. Effect of reaction conditions on cellulose oxidation was investigated. The results showed that high degree of oxidation (DO) and evenly distributed carboxyl could be achieved. The particle size gradually decreased with DO, and oxidized cellulose with high water solubility and amorphous structure could be obtained. Furthermore, FT-IR, 13C NMR and fractionation analysis verified that cellulose was successfully converted and the carboxyl uniformly distributed onto the cellulose chains. This TEMPO-mediated system using LBHs as solvent presented an efficient method on the homogeneous selective oxidation of primary hydroxyl in cellulose.

High-performance flexible resistive random access memory devices based on graphene oxidized with a perpendicular oxidation gradient

The conventional strategy of fabricating resistive random access memory (RRAM) based on graphene oxide is limited to a resistive layer with homogeneous oxidation, and the switching behavior relies on its...

Drinking water treatment and chemical well clogging by iron(II) oxidation and hydrous ferric oxide (HFO) precipitation

Removal of iron(II) from groundwater by aeration and rapid sand filtration (RSF) with the accompanying production of drinking water sludge in the preparation of drinking water from groundwater, and chemical well clogging by accumulation of hydrous ferric oxide (HFO) precipitates and biomass after mixing of oxygen containing and of iron(II) containing groundwater, are identical processes. Iron(II) may precipitate from (ground)water by homogeneous, heterogeneous and/or biological oxidation, where the contribution of these processes, and thus the characteristics of the corresponding HFO precipitates, is a function of pH and process-conditions. Under current conditions in drinking water treatment, homogeneous oxidation dominates above pH ≈ 7.75, and heterogeneous and biological oxidation below this value. In chemical well clogging, this transition occurs at pH ≈ 7.0. This information is relevant for the optimization of removal of iron(II) from groundwater by aeration and RSF and the corresponding quality of the produced drinking water sludge, and for the operation of wells clogging by accumulation of HFO precipitates and biomass.