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Cost-effective and environmental-friendly substrates are essential for the constructed wetlands (CWs). In this study, the column test was used to explore the differences in pollutant purification performance, microbial community structure and abundance between non-burning compound filler and conventional CWs substrates (i.e. gravel and ceramsite) at low temperature (0–15℃). It was found that the maximum phosphorus removal efficiency of compound filler (99%) was better than gravel (18%) and ceramsite (21%). Besides, the proportion of aerobic heterotrophic bacteria capable of ammonium oxidation, nitrification and denitrification (i.e. Pseudomonas, Acinetobacter, and Acetoanaerobium) was enhanced by compound filler, which has an excellent potential for nitrogen removal in the subsequent purification process. These results demonstrated that the self-made non-burning compound filler was a potential substrate for CWs, which was of great significance for the resource utilization of solid wastes such as polyaluminum chloride residue. [ABSTRACT FROM AUTHOR]

The novel iron-based reductive particles, functionalized with amino and carboxylic functional groups, were synthesized to remove Cr(VI) and Cd(II) ions from aqueous solutions. The morphological structure and surface functional groups of new composites were characterized with SEM, XRD, FTIR, BET, and other techniques. The influence of pH, initial concentration, adsorbent dosing, and temperature on removal efficiencies were explored by batch experiments. The adsorption capacity of Cr(VI) and Cd(II) increased by 159.95% and 76.60%, respectively, compared with Fe0, reaching 47.638 and 62.047 mg/g. EDS and XPS analysis showed most of Cr(VI) was reduced to Cr(III) and precipitated as ferrochrome oxide, and Cd(II) was mainly precipitated as hydroxide. Reduction-precipitation and complexation may predominate in the removal process of Cr(VI), which fitted well with Langmuir and Freundlich models and pseudo-second-order kinetics. While hydrolysis and complexation may prevail for Cd(II), which was suited with Langmuir model and pseudo-second-order kinetics. Having good magnetic properties, the A/C-Fe@SiO2 particles exhibited excellent reusable stability after four times regeneration experiments, promising a prospect for in-situ remediations of groundwater contaminated by Cr(VI) and Cd(II). [ABSTRACT FROM AUTHOR]

As an inevitable industrial by-product, polyaluminum chloride residue (PACR) will cause serious harm to the environment if directly buried and dumped. The aim of this paper was searched a new economical, environmental, and practical way of utilization for PACR. In this paper, a novel non-burning PACR compound filler was made from mainly PACR. The prepared compound filler has excellent physical properties and phosphate adsorption efficiency of up to 99.9%. Static adsorption experiments showed that the adsorption process of phosphorus by the compound filler conformed to the pseudo-second-order kinetic model and intra-particle diffusion model. Langmuir and Freundlich isotherm models described the phosphorus adsorption process well, and the maximum phosphate adsorption capacity arrived at 42.55 mg/g. The phosphate adsorption by the compound filler is a spontaneous endothermic process. The main mechanisms are ligand exchange and Lewis acid-base interactions; calcium and aluminum play important roles in the adsorption of phosphorus by the compound filler. Dynamic column experiments showed that as much as 90% of the phosphorus removal by compound filler, and the phosphorus concentration decreased from 1 to ~0.1mg/L. The results provide a new waste resource utilization method for PACR and show the good application potential of prepared compound filler in constructed wetlands. [ABSTRACT FROM AUTHOR]

In this study, the degradation performance of nutrients in zeolite trickling filter (ZTF) with different influent C/N ratios and aeration conditions was investigated. Microaeration was beneficial for enhancing NH4+-N removal performance. Due to the sufficient carbon source supply under a C/N ratio of 8, a high removal efficiency of NH4+-N and TN was simultaneously observed in ZTF. In addition, TN removal mainly occurred at the bottom, which might be explained by the sufficient nutrients available for bacteria to multiply in this zone. The abundant genera were Acinetobacter, Gemmobacter, Flavobacterium, and Pseudomonas, all of which are heterotrophic nitrification-aerobic denitrification (HNAD) bacteria. In addition, biofilm only slowed down the adsorption rate but did not significantly reduce the adsorption capacity of zeolite. Bio-zeolite had NH4+-N well adsorption capacity and bio-desorption capacity. Biological nitrogen removal performance was superior to physicochemical absorption of zeolite. The results suggested that the physicochemical of zeolite and biochemical reactions of microorganism coupling actions may be the main nitrogen transformation pathway in ZTF. Our research provides a reference for further understanding the nitrogen removal mechanism of zeolite bioreactors. [ABSTRACT FROM AUTHOR]