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1.
Bioresour Technol ; 406: 131003, 2024 Jun 24.
Article in English | MEDLINE | ID: mdl-38925406

ABSTRACT

Integrating algae into constructed wetlands (CWs) enhances wastewater treatment, although the results vary. This review evaluates the role of algae in CWs and the performance of different algae-CW (A-CW) configurations based on literature and meta-analysis. Algae considerably improve N removal, although their impact on other parameters varies. Statistical analysis revealed that 70 % of studies report improved treatment efficiencies with A-CWs, achieving average removal rates of 75 % for chemical oxygen demand (COD), 74 % for total nitrogen and ammonium nitrogen, and 79 % for total phosphorus (TP). This review identifies hydraulic retention times, which average 3.1 days, and their varied impact on treatment efficacy. Mixed-effects models showed a slight increase in COD and TP removal efficiencies of 0.6 % every ten days in the A-CWs. Future research should focus on robust experimental designs, adequate algal storage and separation techniques, and advanced modeling to optimize the treatment potential of algae in CWs.

2.
Water Res ; 249: 120989, 2024 Feb 01.
Article in English | MEDLINE | ID: mdl-38101049

ABSTRACT

Quantitatively identifying the primary sources of organic membrane fouling is essential for the effective implementation of membrane technology and optimal water resource management prior to the treatment. This study leveraged carbon stable isotope tracers to estimate the quantitative contributions of various organic sources to membrane fouling in an ultrafiltration system. Effluent organic matter (EfOM) and aquatic natural organic matter (NOM), two common sources, were combined in five different proportions to evaluate their mixed effects on flux decline and the consequent fouling behaviors. Generally, biopolymer (BP) and low molecular weight neutral (LMWN) size fractions - abundantly present in EfOM - were identified as significant contributors to reversible and irreversible fouling, respectively. Fluorescence spectroscopy disclosed that a protein-like component notably influenced overall membrane fouling, whereas humic-like components were predominantly responsible for irreversible fouling rather than reversible fouling. Fluorescence index (FI) and biological index (BIX), common fluorescence source tracers, showed promise in determining the source contribution for reversible foulants. However, these optical indices were insufficient in accurately determining individual source contributions to irreversible fouling, resulting in inconsistencies with the observed hydraulic analysis. Conversely, applying a carbon stable isotope-based mixing model yielded reasonable estimates for all membrane fouling. The contribution of EfOM surpassed 60 % for reversible fouling and increased with its content in DOM source mixtures. In contrast, aquatic NOM dominated irreversible fouling, contributing over 85 %, regardless of the source mixing ratios. This study emphasizes the potential of stable isotope techniques in accurately estimating the contributions of different organic matter sources to both reversible and irreversible membrane fouling.


Subject(s)
Membranes, Artificial , Ultrafiltration , Ultrafiltration/methods , Carbon , Carbon Isotopes , Spectrometry, Fluorescence
3.
J Environ Manage ; 345: 118895, 2023 Nov 01.
Article in English | MEDLINE | ID: mdl-37659370

ABSTRACT

Over the past decade, there has been a substantial increase in research investigating the potential of graphitic carbon nitride (g-C3N4) for various environmental remediations. Renowned for its photocatalytic activity under visible light, g-C3N4 offers a promising solution for treating water pollutants. However, traditional g-C3N4-based photocatalysts have inherent drawbacks, creating a disparity between laboratory efficacy and real-world applications. A primary practical challenge is their fine-powdered form, which hinders separation and recycling processes. A promising approach to address these challenges involves integrating magnetic or floating materials into conventional photocatalysts, a strategy gaining traction within the g-C3N4-based photocatalyst arena. Another emerging solution to enhance practical applications entails merging experimental results with contemporary computational methods. This synergy seeks to optimize the synthesis of more efficient photocatalysts and pinpoint optimal conditions for pollutant removal. While numerous review articles discuss the laboratory-based photocatalytic applications of g-C3N4-based materials, there is a conspicuous absence of comprehensive coverage regarding state-of-the-art research on improved g-C3N4-based photocatalysts for practical applications. This review fills this void, spotlighting three pivotal domains: magnetic g-C3N4 photocatalysts, floating g-C3N4 photocatalysts, and the application of machine learning to g-C3N4 photocatalysis. Accompanied by a thorough analysis, this review also provides perspectives on future directions to enhance the efficacy of g-C3N4-based photocatalysts in water purification.


Subject(s)
Environmental Pollutants , Environmental Restoration and Remediation , Light , Machine Learning , Water
4.
Sci Total Environ ; 843: 157010, 2022 Oct 15.
Article in English | MEDLINE | ID: mdl-35772558

ABSTRACT

Interactions between microplastics (MPs) and humic substances (HS) are inevitable in MP-contaminated aquatic environment because of the ubiquitous presence of HS. In this study, we explored the effects of abiotic and biotic aging processes on the adsorption behavior of aquatic HS on MPs. Aging experiments were conducted using polyethylene (PE) as a representative MP, in which UV irradiation and microbial incubation were applied for 15 to 18 days to mimic the natural abiotic and biotic aging processes. Surface modifications after the aging treatments were evidenced by the appearance of CO, CO, O-C=O, and -OH groups; the formation of grooves on UV-aged PE; and the formation of biofilms on the surface of bio-aged PE. The specific surface areas of both treated PE MPs increased with aging. Higher HS adsorption on PE surface was observed after the aging treatments, with a highest kinetic rate for UV-aged PE than that for bio-aged PE. The adsorption isotherm models revealed that the aging processes enhanced the HS adsorption tendency, as evidenced by the highest adsorption capacity for UV-aged PE (~187 µg C/m2), followed by bio-aged PE (~157 µg C/m2) and pristine PE (~87.5 µg C/m2) for a comparable extended aging period (15-18 days). The difference was more pronounced at a lower pH. The enhanced HS adsorption was mainly attributed to the formation of hydrogen bonds, whereas HS adsorption on pristine PE was dominated by hydrophobic interactions and weak van der Waals interactions. Among the two identified fluorescent components (terrestrial humic-like C1 and protein-like C2), C1 exhibited a higher affinity for adsorption onto PE irrespective of aging. Our findings provide insights into the substantial changes that occur in the interactions between MPs and aquatic organic matter with aging processes, which may alter the fate and environmental impacts of MPs in many aquatic systems.


Subject(s)
Microplastics , Water Pollutants, Chemical , Adsorption , Humic Substances , Plastics , Polyethylene/chemistry , Water Pollutants, Chemical/analysis
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