The ever-growing contamination of surface water due to various catchment activities poses threats and stress to downstream water treatment entities. Specifically, the presence of ammonia, microbial contaminants, organic matter, and heavy metals has been an issue of paramount concern to water treatment entities since stringent regulatory frameworks require these pollutants to be removed prior to water consumption. Herein, a hybrid approach that integrates struvite crystallization (precipitation) and breakpoint chlorination (stripping) for the removal of ammonia from aqueous solution was evaluated. To fulfil the goals of this study, batch experimental studies were pursued through the adoption of the well-known one-factor-at-a-time (AFAAT) method, specifically the effects of time, concentration/dosage, and mixing speed. The fate of chemical species was underpinned using the state-of-the-art analytical instruments and accredited standard methods. Cryptocrystalline magnesium oxide nanoparticles (MgO-NPs) were used as the magnesium source while the high-test hypochlorite (HTH) was used as the source of chlorine. From the experimental results, the optimum conditions were observed to be, i.e., Stage 1 - struvite synthesis, 110 mg/L of Mg and P dosage (concentration), 150 rpm of mixing speed, 60 min of contact time, and lastly, 120 min of sedimentation while optimum condition for the breakpoint chlorination (Stage 2) were 30 min of mixing and 8:1 Cl:NH weight ratio. Specifically, in Stage 1, i.e., MgO-NPs, the pH increased from 6.7 to ≥9.6, while the turbidity was reduced from 9.1 to ≤1.3 NTU. Mn removal efficacy attained ≥97.70% (reduced from 174 μg/L to 4 μg/L) and Fe attained ≥96.64% (reduced from 11 mg/L to 0.37 mg/L). Elevated pH also led to the deactivation of bacteria. In Stage 2, i.e. breakpoint chlorination, the product water was further polished by eliminating residual ammonia and TPC at 8:1 Cl-NH weight ratio. Interestingly, ammonia was reduced from 6.51 to 2.1 mg/L in Stage 1 (67.74% removal) and then from 2.1 to 0.002 mg/L post breakpoint chlorination (99.96% removal), i.e., stage 2. Overall, synergistic and complementary effects of integrating struvite synthesis and breakpoint chlorination hold great promise for the removal of ammonia from aqueous solutions thus confirming that this technology could potentially be used to curtail the effects of ammonia in the receiving environments and drinking water.
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http://dx.doi.org/10.1016/j.jenvman.2023.117506 | DOI Listing |
Environ Sci Technol
November 2024
Institute of Environmental Engineering, National Yang Ming Chiao Tung University, Hsinchu city 30010, Taiwan.
Chlorination of ammonia or chloramine-containing waters induces breakpoint chlorination reactions, producing a hydroxyl radical (•OH), but enhances the formation of undesirable -nitrosamines. The prevailing view attributes •OH formation to a nitrosyl intermediate derived from the hydrolysis of dichloramine, but this pathway is unlikely at neutral or acidic pH. This study reveals a novel mechanism where •OH is generated via interactions between trichloramine (NCl) and dichloramine (NHCl), which also form nitrosation agents.
View Article and Find Full Text PDFFront Microbiol
September 2024
Department of Biochemistry, Faculty of Science, University of Geneva, Geneva, Switzerland.
Introduction: (Mtb), the causative agent of tuberculosis, remains a serious threat to human health worldwide and the quest for new anti-tubercular drugs is an enduring and demanding journey. Natural products (NPs) have played a significant role in advancing drug therapy of infectious diseases.
Methods: This study evaluated the suitability of a high-throughput infection system composed of the host amoeba (Dd) and (Mm), a close relative of Mtb, to identify anti-infective compounds.
Sci Rep
September 2024
College of Environment and Safety Engineering, Qingdao University of Science and Technology, Qingdao, 266042, China.
Nitrate can be electrolyzed mainly into N, but the generated ammonia, as its secondary intermediate, is soluble and remained in the wastewater yet, which affects negatively the degradation of nitrate and total nitrogen. In this work, an electrolytic reactor constructed with Ti/RuSn anode and Fe cathode, was applied to electrolyze nitrate, and magnesium chloride was used as electrolyte and precipitant simultaneously, while disodium hydrogen phosphate (DSP) was added only as precipitant of ammonia. The results indicated that, most part of generated ammonia could be precipitated as magnesium ammonium phosphate (MAP) and some residual ammonia may be transformed into N by breakpoint chlorination.
View Article and Find Full Text PDFJ Colloid Interface Sci
December 2024
Institute for Ecological Research and Pollution Control of Plateau Lakes, School of Ecology and Environmental Science, Yunnan University, Kunming 650504, China. Electronic address:
The electrocatalytic reduction of nitrate ions (NO) to nitrogen gas (N) has emerged as an effective approach for mitigating nitrate pollution in water bodies. However, the development of efficient and highly selective cathode materials remains challenging. Conventional copper-based catalysts often exhibit low selectivity because they strongly adsorb oxygen.
View Article and Find Full Text PDFChemosphere
April 2024
Department of Civil and Construction Engineering, Curtin University, GPO Box U1987, Perth, WA, 6845, Australia; School of Engineering, Design and Built Environment, Western Sydney University, Locked Bag 1797, Penrith, NSW, 2751, Australia. Electronic address:
This paper highlights the potential to effectively inhibit nitrification and restore chloramine levels using a low copper concentration in a biofilm-affected (surface-to-volume ratio 16 m) continuous-flow laboratory-scale chloraminated system. High nitrite and low chloramine containing tanks are always recovered with chlorine "burn" by water utilities. The "burn" is not only costly and operationally complex, but also compromises the water quality, public health, and customer relations.
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