Exploring acid mine drainage treatment through adsorption: a bibliometric analysis.

Discharge of acidic wastewater from mining activities (acid mine drainage (AMD)) is a major global environmental and public health issue. Although several approaches, including chemical precipitation and membrane technology, have been developed to treat AMD, adsorption has emerged as the most promising technology due to its cost-effectiveness and efficacy. Despite the wide adoption of adsorption in treating AMD, the evolution of research in this area remains poorly understood. To address this gap, a bibliometric analysis of the most recent literature involving the application of adsorption in AMD remediation was conducted by merging datasets of articles from Scopus (1127) and the Web of Science Core Collection (1422), over the past decade (2013-2022). This analysis revealed a yearly increase of 11% in research publications, primarily contributed by China, the United States, and South Africa. Keyword analysis revealed that natural schwertmannites and their transformations, activated carbon, zeolites, and clay minerals, are the most extensively employed adsorbents for the removal of common metals (arsenic, chromium, iron, manganese, among others). The findings underscore the need for future focuses on recovering rare earth elements, using nanoparticles and modified materials, pursuing low-cost, sustainable solutions, integrating hybrid technologies, pilot-scale studies, exploring circular economic applications of AMD sludges, and inter-continental collaborations. These insights hold significant future implications, serving as a valuable reference to stakeholders in the mining industry.

CFD-Assisted Process Optimization of an Integrated Photocatalytic Membrane System for Water Treatment.

An integrated photocatalytic membrane system (IPMS) was developed for potential use in the remediation of naproxen using real water samples from a drinking water treatment plant. Key parameters such as time, pH, water matrix, mixing speeds, flow rate, and light intensity undeniably affected photocatalytic and membrane separation processes. The system optimization was based on improving irradiation to generate a more reactive species and mass transfer to increase the reaction rate. Upon optimization, IPMS achieved 99% naproxen removal efficiency. Computational fluid dynamics (CFD) simulated the flow patterns and radiation distribution inside the photocatalytic membrane reactor to improve irradiation and mass transfer during operation. The simulated flow field revealed the presence of dead zones with different velocities in the photocatalytic membrane reactor; this limited the mass transfer of reactive species in the reactor, resulting in uneven distribution of reactive radicals. The dead zones were mitigated by increasing the mixing speed, and as a result, convective mass flow improved process performance. The governing parameters (flow patterns and radiation distribution) of the simulated and experimental data were in agreement. The absorption of irradiation by the active site of the membranes improved with light intensity; at higher light intensities, the light irradiated deeper into the membrane. As such, the CoFe2O4 nanoparticles incorporated inside the membrane pores became highly activated, thus enhancing degradation. The obtained space-time yield (STY) (1.23 × 1011 mol/cm2.s) and photocatalytic space-time yield (PSTY) (4.39 × 1011 mol/W.s) showed that the developed IPMS was efficient regarding energy intensiveness and throughput for treatment of pollutants in water.

Role of Membrane-Solute Affinity Interactions in Carbamazepine Rejection and Resistance to Organic Fouling by Nano-Engineered UF/PES Membranes.

In this study, polyethersulfone (PES) ultrafiltration (UF) membranes were modified with GO, Ag, ZnO, Ag-GO and ZnO-GO nanoparticles to improve carbamazepine removal and fouling prevention by making membrane surfaces more hydrophilic. The fabricated membranes were characterized for surface and cross-sectional morphology, surface roughness and zeta potential, as well as hydrophilicity, functional groups, surface tension parameters and water permeability Thereafter, the membranes were evaluated for their efficiency in removing MgSO4 and carbamazepine as well as antifouling properties. To understand the role of affinity interactions in rejection and fouling, membrane-solute adhesion energies (∆Gslm) were quantified based on the Lifshitz-van der Waals/acid-base method. Unlike previous studies, which have generalized fouling prevention to be due to improvements in hydrophilicity upon adding nanoparticles, this work further explored the role of surface tension components on rejection and fouling prevention. The addition of nanoparticles improved membrane hydrophilicity (77-62°), water permeability (11.9-17.7 Lm-2 h-1 bar-1), mechanical strength (3.46-4.11 N/mm2), carbamazepine rejection (30-85%) and fouling prevention (60-23% flux decline). Rejection and antifouling properties increased as ∆Gslm became more repulsive (i.e., less negative). Membrane modification reduced irreversible fouling, and the fouled membranes were cleaned by flushing with water. Fouling related more to membrane electron donor components (γ-), while the roles of electron acceptor (γ+) and Lifshitz-van der Waals components (γLW) were less important. This work provides more insights into the role of affinity interactions in rejection and fouling and how rejection and fouling mechanisms change with nanoparticle addition.

The synergistic effect of peracetic acid activated by graphene oxide quantum dots in the inactivation of E. coli and organic dye removal with LED reactor light.

This study presents a low-impact process that uses the synergy of peracetic acid (PAA) and graphene oxide quantum GQDs to degrade poorly biodegradable organic compounds and potentially substitute chlorination in wastewater treatment. The role of GQDs in GQDs/PAA activity and the effect of GQDs loading were examined. The results showed that increasing GQDs loading in the GQDs/PAA system greatly improved the photodegradation efficiency. Conversely, increasing the PAA concentration slightly enhanced efficiency due to few active sites being available. GQDs acted as catalysts and radical scavenging experiments confirmed that the degradation occurred via generation of hydroxyl (•OH) and peroxy (CH3C(=O)OO•)) radicals. A probable degradation mechanism of the organic dye was presented based on the reaction by-products detected after HPLC-MS studies. The E. coli inactivation mechanism was elucidated by monitoring the morphological changes of E. coli using scanning microscopy. The proposed antimicrobial mechanism includes the initial diffusion of PAA through the cell membrane which caused damage and induced cellular matter leakage, resulting in cell death. Bacterial regrowth studies confirmed GQDs/PAA were able to bypass the natural mechanisms of microorganisms that enables them to repair any damages in their DNA.

A review on water treatment technologies for the management of oxoanions: prospects and challenges.

Oxoanions are a class of contaminants that are easily released into the aquatic systems either through natural or anthropogenic activities. Depending on their oxidation states, they are highly mobile, resulting in the contamination of underground water. Above the permissible level in groundwater, they pose as threats to mammals when the contaminated water is consumed. Some of the health challenges caused are cancer, neurological, cardiac, gastrointestinal, and skin disorders. Several treatment technologies have been adopted over the years for the management of these oxoanions present in the aquatic systems. However interesting these treatment technologies might be, they also have their limitations such as cost-effectiveness, the complexity of the process, and generation of secondary pollutants. This work focused on some of the water treatment technologies applied for the removal of oxoanions. Some of the advantages and disadvantages of these treatment technologies are also highlighted. Amongst all the treatment technologies, adsorption is the most applied method for the removal of oxoanions. However, photocatalysis has a higher prospect since it is non-selective and secondary pollutants are not generated after the treatment process. Also, photocatalysis can simultaneously reduce and oxidise oxoanions as well as organic pollutants respectively.

Interdependence of Contributing Factors Governing Dead-End Fouling of Nanofiltration Membranes.

Cake-enhanced concentration polarization (CECP) has been ascribed as the main cause of flux decline in dead-end filtration. An unfamiliar approach was used to investigate the role of CECP effects in the fouling of a nanofiltration membrane (NF-270) that poorly reject salts. Membrane-foulant affinity interaction energies were calculated from measured contact angles of foulants and membrane coupons based on the van der Waals/acid-base approach, and linked to resistance due to adsorption (Ra ). In addition, other fouling mechanisms and resistance parameters were investigated using model organic and colloidal foulants. After selection, the foulants and membranes were characterized for various properties, and fouling experiments were conducted under controlled conditions. The fouled membranes were further characterized to gain more understanding of the fouling layer properties and flux decline mechanisms. Sodium alginate and latex greatly reduced membrane permeate flux as the flux declined by 86% and 59%, respectively, while there was minor flux decline when aluminum oxide was used as model foulant (<15% flux decline). More flux decline was noted when fouling was conducted with a combination of organic and colloidal foulants. Contrary to other studies, the addition of calcium did not seem to influence individual and combined fouling trends. Foulants adsorbed more on the membrane surface as the membrane-foulant affinity interactions became more attractive and pore blocking by the foulants was not important for these experiments. Hydraulic resistance due to cake formation (Rc ) had a higher contributing effect on flux decline, while CECP effects were not substantial.

Unraveling bacterial diversity in oil refinery effluents.

Oil refinery effluents are among stressful environments, and they are characterized by alkaline pH, high concentrations of dissolved solids, electrical conductivity, and metals (mainly Fe, Al, B, Sr, Mn, Cu, Ni). In this study, bacterial diversity in these habitats was inferred from full-length 16S rRNA gene sequences obtained from the PacBio® sequencing platform. The results have shown low bacterial diversity in both raw and treated effluents, with sequences representing only two phyla: Firmicutes and Proteobacteria. Sequences from the raw effluents represent four major genera: Bacillus, Wenzhouxiangella, Rhodabaculum, and Halomonas. Whilst bacterial communities from the treated effluents are relatively more diverse as sequences represent five dominant genera: Pseudoxanthomonas, Brevundimonas, Pseudomonas, Rhodobaculum and Rhizobium. Most of the genera represented in the dataset are halophilic or halotolerant microbes known to have the competency to catabolize a broad spectrum of organic and inorganic pollutants. Hypothetically, these bacteria may be relevant for biotechnological and industrial applications, particularly for the remediation of saline industrial wastes.

Novel hybrid metal loaded chelating resins for removal of toxic metals from acid mine drainage.

Iron (Fe), zirconium (Zr) and titanium (Ti) oxides nanoparticles were each embedded onto a weak acid chelating resin for support using the precipitation method to generate three hybrid adsorbents of hydrated Fe oxide (HFO-P), hydrated Zr oxide (HZO-P) and hydrated Ti oxide (HTO-P). This paper reports on the characterization, performance and potential of these generated nanoadsorbents in the removal of toxic metal ions from acid mine drainage (AMD). The optimum contact time, adsorbent dose and pH for aluminium (Al) (III) adsorption were established using the batch equilibrium technique. The metal levels were measured using inductively coupled plasma-optical emission spectrometry. The scanning electron microscopy-energy dispersive X-ray spectroscopy results confirmed the presence of the metal oxides within the hybrid resin beads. HFO-P, HZO-P and HTO-P adsorbed Al(III) rapidly from synthetic water with maximum adsorption capacities of 54.04, 58.36 and 40.10 mg/g, respectively, at initial pH 1.80 ± 0.02. The adsorption of Al(III) is of the second-order in nature (R2 > 0.98). The nanosorbents removed ten selected metals from environmental AMD and the metal removal efficiency was in the order HTO-P > HZO-P > HFO-P. All three hybrid nanosorbents can be used to remove metals from AMD; the choice would be dependent on the pH of the water to be treated.

Polymeric ion exchanger supported ferric oxide nanoparticles as adsorbents for toxic metal ions from aqueous solutions and acid mine drainage.

BACKGROUND: Acid mine drainage (AMD) is a worldwide industrial pollution of grave concern. AMD pollutes both water sources and the environment at large with dissolved toxic metals which are detrimental to human health. This paper reports on the preparation of polymeric ion exchange resins decorated with hydrated iron oxides and their application for the ecological removal of toxic metals ions from AMD. METHODS: The hydrated iron oxide particles were incorporated within commercial chelating ion exchange resins using the precipitation method. The synthesised hybrid resins were then characterized using appropriate spectroscopic and solid-state techniques. The metal ion levels were measured using the inductively coupled plasma-optical emission spectrometer (ICP-OES). The optimization of contact time, pH, and adsorbent dosage were conducted to enhance the efficiency of adsorption of toxic metals onto the hybrid organic/inorganic nanosorbents. Kinetics and adsorption isotherms were constructed to study the adsorption mechanisms of the adsorbents. RESULTS: The results showed that the dispersed Fe-O is hydrated and amorphous within the hybrid materials. The adsorption kinetics followed the pseudo-second-order shown by the high R2 values. The hybrid adsorbents were finally tested on environmental AMD samples and were able to remove toxic metals Al, Cd, Co, Cr, Cu, Fe, Mn, Ni, Pb and Zn at various removal degrees. CONCLUSION: Solution pH played a crucial role in the adsorption of toxic metals on hybrid iron oxide adsorbents. The hybrid TP-260 HFO had higher affinity for toxic metals than other prepared adsorbents thus has a potential for acidic mine water pollution remediation. The adsorbed Al(III) can be recovered using NaCl-NaOH binary solution from the loaded resins.

PAMAM templated N,Pt co-doped TiO2 for visible light photodegradation of brilliant black.

This study examined the photocatalytic degradation of an azo dye brilliant black (BB) using non-metal/metal co-doped TiO2. N,Pt co-doped TiO2 photocatalysts were prepared by a modified sol-gel method using amine-terminated polyamidoamine dendrimer generation 0 (PG0) as a template and source of nitrogen. Structural, morphological, and textural properties were evaluated using scanning electron microscopy coupled to energy-dispersive X-ray spectroscopy (SEM/EDX), high-resolution transmission electron microscopy (HRTEM), X-ray diffraction spectroscopy (XRD), X-ray photoelectron spectroscopy (XPS), thermal gravimetric analysis (TGA), Fourier transform infrared (FTIR), Raman spectroscopy (RS), photoluminescence (PL) and ultra-violet/visible spectroscopy (UV-Vis). The synthesized photocatalysts exhibited lower band gap energies as compared to the Degussa P-25, revealing a red shift in band gap towards the visible light absorption region. Photocatalytic activity of N,Pt co-doped TiO2 was measured by the reaction of photocatalytic degradation of BB dye. Enhanced photodegradation efficiency of BB was achieved after 180-min reaction time with an initial concentration of 50 ppm. This was attributed to the rod-like shape of the materials, larger surface area, and enhanced absorption of visible light induced by N,Pt co-doping. The N,Pt co-doped TiO2 also exhibited pseudo-first-order kinetic behavior with half-life and rate constant of 0.37 and 0.01984 min-1, respectively. The mechanism of the photodegradation of BB under the visible light irradiation was proposed. The obtained results prove that co-doping of TiO2 with N and Pt contributed to the enhanced photocatalytic performances of TiO2 for visible light-induced photodegradation of organic contaminants for environmental remediation. Therefore, this work provides a new approach to the synthesis of PAMAM templated N,Pt co-doped TiO2 for visible light photodegradation of brilliant black.

The impact of microbial ecology and chemical profile on the enhanced biological phosphorus removal (EBPR) process: a case study of Northern Wastewater Treatment Works, Johannesburg.

The impact of polyphosphate-accumulating organism (PAO) and glycogen-accumulating organism (GAO) populations as well as of the chemical profile on the performance of Unit-3 (open elutriation tanks) and Unit-5 (covered elutriation tank) of the City of Johannesburg Northern Wastewater Treatment Works was determined. Physicochemical parameters of wastewater samples were measured using standard methods. Bacterial diversity was determined using 16S rRNA gene amplicon pyrosequencing of the variable region V1-3. Results showed soluble COD concentrations from settled sewage for Unit-3 at 192.8 mg COD/L and for Unit-5 at 214.6 mg COD/L, which increased to 301.8 mg COD/L and 411.6 mg COD/L in the overflow from elutriation tanks and decreased to 170.9 mg COD/L and 256.3 mg COD/L at the division boxes, respectively. Both long-chain volatile fatty acids (heptanoic acid, isobutyric acid, 3-methylbutanoic acid, pentanoic acid, 4-methylpentanoic acid, methylheptanoic acid) and short-chain volatile fatty acids (acetic acid, propionic acid, isobutyric acid) were present within concentration ranges of 17.19 mg/L to 54.98 mg/L and 13.64 mg/L to 87.6 mg/L for Unit 3 and 38.61 mg/L to58.85 mg/L and 21.63 mg/L to 92.39 mg/L for Unit 5, respectively. In the secondary settling tanks, the phosphate-removal efficiency in Unit-5 appeared to be slightly higher (0.08 mg P/L) compared to that of Unit-3 (0.11 mg P/L). The average DO concentrations (2.1 mg/L and 2.2 mg/L) as well as the pH values (pH 7 to pH 7.5) were found to be slightly higher in Unit-5 in the aerobic zones. The high presence of PAOs in the bioreactors (Unit-5: Dechloromonas (14.96%), Acinetobacter (6.3%), Zoogloea (4.72%) in the anaerobic zone and Dechloromonas (22.37 %) in the aerobic zone; Unit-3: Dechloromonas (37.25%) in the anaerobic zone and Dechloromonas (23.97%) in the aerobic zone) confirmed the phosphate-removal efficiencies of both units. Negligible GAOs were found in the aerobic zones (Defluviicoccus spp.: 0.33% for Unit-5 and 0.68% for Unit-3) and in the anaerobic zones (Defluviicoccus: 9.8% for Unit-3). The high microbial diversity and a negligible percentage of GAOs in Unit-5 could contribute to its high phosphate-removal efficiency, although results did not indicate statistically significant differences between the unit with a covered elutriation tank (Unit-5) and that with open elutriation tanks (Unit-3).