Biochar usage for removing heavy metals from aqueous environments has emerged as a promising research area with significant environmental and economic benefits. Using the PICO approach, the research question aimed to explore using biochar to remove heavy metals from aqueous media. We merged the data from Scopus and the Web of Science Core Collection databases to acquire a comprehensive perspective of the subject. The PRISMA guidelines were applied to establish the search parameters, identify the appropriate articles, and collect the bibliographic information from the publications between 2010 and 2022. The bibliometric analysis showed that biochar-based heavy metal remediation is a research field with increasing scholarly attention. The removal of Cr(VI), Pb(II), Cd(II), and Cu(II) was the most studied among the heavy metals. We identified five main clusters centered on adsorption, water treatment, adsorption models, analytical techniques, and hydrothermal carbonization by performing keyword co-occurrence analysis. Trending topics include biochar reusability, modification, acid mine drainage (AMD), wastewater treatment, and hydrochar. The reutilization of heavy metal-loaded spent biochar includes transforming it into electrodes for supercapacitors or stable catalyst materials. This study provides a comprehensive overview of biochar-based heavy metal remediation in aquatic environments and highlights knowledge gaps and future research directions.

Acid mine drainage (AMD) is a major environmental problem caused by the release of acidic, toxic, and sulfate-rich water from mining sites. This study aimed to develop novel adsorbents for the removal of chromium (Cr(VI)), cadmium (Cd(II)), and lead (Pb(II)) from simulated and actual AMD using hybrid ion-exchange resins embedded with hydrous ferric oxide (HFO). Two types of resins were synthesized: anionic exchange resin (HAIX-HFO) for Cr(VI) removal and cationic exchange resin (HCIX-HFO) for Cd(II) and Pb(II) removal. The resins were characterized using scanning electron microscopy and Raman spectroscopy, which confirmed the presence of HFO particles. Batch adsorption experiments were conducted under acidic and sulfate-enhanced conditions to evaluate the adsorption capacity and kinetics of the resins. It was found that both resins exhibited high adsorption efficiencies and fast adsorption rates for their respective metal ions. To explore the potential adsorption on actual AMD, HCIX-HFO demonstrated significant removal of some metal ions. The saturated HCIX-HFO resin was regenerated using NaCl, and a high amount of the adsorbed Cd(II) and Pb(II) was recovered. This study demonstrates that HFO-embedded hybrid ion-exchange resins are promising adsorbents for treating AMD contaminated with heavy metals.

Arid areas often contain brackish groundwater that has a salinity exceeding 500 mg/L. This poses several challenges to the users of the water such as a salty taste and damage to household appliances. Desalination can be one of the key solutions to significantly lower the salinity and solute content of the water. However, the technology requires high energy inputs as well as managing waste products. This paper presents the fabrication of ultrafiltration heterogeneous ion exchange membranes for brackish groundwater treatment. Scanning electron microscopy (SEM) images showed a relatively uniform resin particle distribution within the polymer matrix. The mean roughness of the cation exchange membrane (CEM) and anion exchange membrane (AEM) surfaces increased from 42.12 to 317.25 and 68.56 to 295.95 nm, respectively, when resin loading was increased from 1 to 3.5 wt %. Contact angle measures suggested a more hydrophilic surface (86.13 to 76.26° and 88.10 to 74.47° for CEM and AEM, respectively) was achieved with greater resin loading rates. The ion exchange capacity (IEC) of the prepared membranes was assessed using synthetic groundwater in a dead-end filtration system and removal efficiency of K⁺, Mg²⁺, and Ca²⁺ were 56.0, 93.5, and 85.4%, respectively, for CEM with the highest resin loading. Additionally, the anion, NO₃⁻ and SO₄²⁻ removal efficiency was 84.2% and 52.4%, respectively, for the AEM with the highest resin loading. This work demonstrates that the prepared ultrafiltration heterogeneous ion exchange membranes have potential for selective removal for of ions by ion exchange, under filtration conditions at low pressure of 0.05 MPa.

Microplastics have emerged as pervasive contaminants in various ecosystems, raising considerable concerns regarding their impact on environmental health and public safety. The degradation of microplastics is thus recognized as a pressing global challenge. Photocatalytic degradation has emerged as a promising approach due to its potential for efficiency and environmental sustainability. Nevertheless, there remains a need to investigate emerging trends and advancements to understand and fully optimize this technique. Consequently, PRISMA guidelines were employed to define the search parameters, enable the identification of pertinent scholarly articles, and systematically gather bibliographic data from the published literature from 2005 to October 2024. A bibliometric analysis of 204 research articles derived from merged Scopus and Web of Science datasets was conducted to map the field’s research landscape. The analysis showed a robust annual publication growth rate of 17.94%, with leading contributions from China, India, Mexico, and the United Kingdom. Keyword analysis revealed that the commonly applied photocatalysts are titanium dioxide and zinc oxide in the photocatalytic degradation of polyethylene terephthalate, polypropylene, polystyrene, polyvinyl chloride, high-density polyethylene, and low-density polyethylene. Advances in collaboration across Asia and Europe have bolstered the research landscape. However, challenges persist in achieving cost-effective scalability, ensuring the safety of degradation byproducts, and translating laboratory findings into real-world applications. Emerging trends include the development of visible-light-responsive catalysts, advanced nanocomposites, and sustainable photocatalytic technologies. This study underscores the utility of bibliometric tools in identifying knowledge gaps and guiding the development of innovative approaches for microplastic degradation as part of environmental remediation efforts.

Industries frequently discharge elevated levels of lead and cadmium into the environment, posing significant threats to ecological balance and public health. This study developed a novel polycaprolactone–chitosan–montmorillonite (PCL/CS/MMT) composite to adsorb Pb(II) and Cd(II) from aqueous solutions. The composite was synthesized via twin‐screw melt extrusion and subsequently characterized using X‐ray diffraction (XRD), scanning electron microscopy (SEM), energy‐dispersive X‐ray spectroscopy (EDS), Fourier transform infrared spectroscopy (FTIR), and thermogravimetric analysis (TGA), revealing a crystalline structure, cracked surface morphology, functionalized surface groups, and thermal stability. Under optimal batch conditions, the adsorbent achieved maximum adsorption capacities of 12.35 mg/g for Pb(II) and 16.92 mg/g for Cd(II). Adsorption behavior followed the Langmuir isotherm model, and kinetic data aligned with the pseudo second‐order model, indicating a chemisorption‐driven mechanism. The composite demonstrated effective regeneration, retaining over 55% adsorption efficiency after seven desorption cycles with 0.1 M (pH 8). These findings position the PCL/CS/MMT composite as a promising, sustainable adsorbent for wastewater treatment, offering a viable solution to heavy metal pollution and advancing the development of eco‐friendly materials for environmental remediation.