For groundwater treatment, the technologies involving oxidation on MnOx filter bed are beneficial, common, and effectively used. The presence of MnOx is the mutual feature of filter media, both MnOx-coated mineral materials like quartz sand and gravel, chalcedonite, diatomite, glauconite, zeolite, or anthracite along with consisting of MnOx manganese ores. This review is based on the analysis of research and review papers, commercial data sheets, and standards. The paper aimed to provide new suggestions and useful information for further investigation of MnOx filter media for groundwater treatment. The presented compilations are based on the characteristics of coatings, methods, and conditions of its obtaining and type of filter media. The relationship between the properties of MnOx amendments and the obtained purification effects as well as the commonly used commercial products, their features, and applications have been discussed. The paper concludes by mentioning about improving catalytic/adsorption properties of non-reactive siliceous media opposed to ion-exchange minerals and about possible significance of birnessite type manganese oxide for water treatment. Research needs related to the assessment of the use MnOx filter media to heavy metals removal from groundwater in field operations and to standardize methodology of testing MnOx filter media for water treatment were identified.
A high concentration of aggressive carbon dioxide disturbs many technological processes in water treatment. It also causes the development of corrosion in steel and concrete. De-acidification of groundwater by means of air bubbles alters pH and the concentration of aggressive carbon dioxide. This was investigated for the variables of air flow (Q = 20–50 L h−1) and height of water layer (H = 25–75 cm) as well as aeration time (t = 0–20 min). The obtained three-parameter models showed good correlation with the experimental results, except in a few cases where r2 was bigger than 0.9. Furthermore, they allow for prediction of an increase of pH and a decrease in concentration of aggressive carbon dioxide in aerated water. The effectiveness of de-acidification of groundwater was evaluated using indices of water stability (Langelier Saturation Index, Precipitation Index, Ryznar Stability Index, Aggressiveness Index and Index of Aggressiveness). Although as a result of aeration an increase of pH over 7 was observed, the non-corrosive values of the indices were not reached. This was due to a very low alkalinity of water, which was 0.7 meq L−1.
The study aimed to determine the nature of the kinetics of the manganese sorption process on Ukrainian tuff and basalt at different temperatures characteristic of the natural water environment. The scope of the research included manganese sorption kinetic test on natural mineral sorbents at temperatures of 10, 17.5 and 25 °C in slightly acidic conditions. Sorption (pseudo-first order, pseudo-second order and Elovich models) and diffusion kinetic models (liquid film diffusion and intraparticle diffusion) were used in the analysis of test results. The manganese sorption process on both tuff and basalt proceeded quickly. The dynamic equilibrium state of manganese sorption settled after 35 and 45 min on tuff and basalt respectively. Although the process took place in a slightly acidic environment and below pHPZC of the sorbents, possible electrostatic repulsion did not inhibit the removal of Mn. The Mn sorption on both materials followed the PSO kinetics model. Based on the diffusion kinetic models, it was determined that Mn sorption process on both materials was influenced by diffusion through the boundary layer and intraparticle diffusion. The differences in removal efficiency and rate of Mn sorption in the temperature range of 10–25 °C were not found.
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