Remediation Methods Research Articles

The Effect of Using Error Analysis as a Remedial Teaching Strategy on English Major Students’ Productive Skills

The objective of this study was to examine the impact of employing Error Analysis as a remedial teaching method on the productive skills of English Major Students. The study included thirty-six students enrolled in the Department of English Language and Literature at Al-Isra University during the first semester of the academic year 2022/2023. The study participants were initially divided into two sections: section A, comprising thirty students who registered for the Syntax Course, which was assigned as the experimental group. The material was taught using Error Analysis as a remedial teaching method. Section B comprised sixteen students who enrolled in the Applied Linguistics Course. The control group was chosen and instructed using conventional teaching methods. A pre/post-test was administered to evaluate the impact of utilizing error analysis as a remedial teaching method on enhancing the productive skills of English as a Foreign Language (EFL) students. Both groups of students took a pre-test to determine their equivalence prior to commencing the experiment. Following a duration of eight weeks, the identical test was administered to both groups as a post-test in order to evaluate their progress in the Productive skills. The statistical analysis employed included measures, standard deviation, T-test, One-way ANOVA, and Scheffe. The study's findings demonstrated that implementing Error Analysis as a method of Remedial Teaching had a notable impact on enhancing students' Productive skills. The findings also demonstrated a clear advantage for the experimental group. This could be attributed to the impact of employing Error Analysis as a method of Remedial Teaching. Consequently, a set of recommendations was given at the conclusion of the study to promote the use of Error Analysis as a strategy for Remedial Teaching in order to enhance the development of productive skills in English Major students.

A Novel Cold-Adapted Nitronate Monooxygenase from Psychrobacter sp. ANT206: Identification, Characterization and Degradation of 2-Nitropropane at Low Temperature

Aliphatic nitro compounds cause environmental pollution by being discharged into water with industrial waste. Biodegradation needs to be further explored as a green and pollution-free method of environmental remediation. In this study, we successfully cloned a novel nitronate monooxygenase gene (psnmo) from the genomic DNA library of Psychrobacter sp. ANT206 and investigated its ability to degrade 2-nitropropane (2-NP). Homology modeling demonstrated that PsNMO had a typical I nitronate monooxygenase catalytic site and cold-adapted structural features, such as few hydrogen bonds. The specific activity of purified recombinant PsNMO (rPsNMO) was 97.34 U/mg, rPsNMO exhibited thermal instability and reached maximum catalytic activity at 30 °C. Moreover, rPsNMO was most active in 1.5 M NaCl and remained at 104% of its full activity in 4.0 M NaCl, demonstrating its significant salt tolerance. Based on this finding, a novel bacterial cold-adapted enzyme was obtained in this work. Furthermore, rPsNMO protected E. coli BL21 (DE3)/pET28a(+) from the toxic effects of 2-NP at 30 °C because the 2-NP degradation rate reached 96.1% at 3 h and the final product was acetone. These results provide a reliable theoretical basis for the low-temperature degradation of 2-NP by NMO.

Groundwater Contamination by Heavy Metals in Malaysia: Sources, Transport, and Remediation Strategies

Groundwater contamination by heavy metals is a pressing environmental concern, particularly in regions highly dependent on groundwater as a freshwater source. While Malaysia primarily relies on river water, certain states and islands depend on groundwater for their supply. Research on heavy metal contamination in Malaysia’s groundwater remains limited, making it crucial to study the distribution and mobility of contaminants to develop appropriate remediation strategies. In addition to natural sources, anthropogenic activities such as landfills, mining, and the use of fertilizers contribute significantly to heavy metal pollution in groundwater. Factors like rainfall, fluctuating groundwater levels, and low soil pH can exacerbate heavy metal leaching into aquifers. Various models and techniques, including 2D resistivity imaging and MODFLOW, are used to assess groundwater flow and contaminant transport. These models suggest that contaminant concentrations decrease with increased depth and radial distance from pollution sources such as landfills and mining areas. The health risks associated with heavy metal exposure through groundwater consumption are significant, necessitating effective remediation strategies. Phytoremediation is an economical solution for groundwater containing low concentrations of heavy metals, while permeable reactive barriers may be suitable for more complex cases, pending detailed site investigation. This review aims to examine the current state of knowledge on heavy metal contamination in Malaysia’s groundwater, focusing on sources, distribution patterns, and movement of pollutants. It also seeks to evaluate existing remediation methods, including phytoremediation and permeable reactive barriers, while identifying gaps in research, particularly concerning risk assessments and heavy metal speciation.

Research Progress on Physical and Chemical Remediation Methods for the Removal of Cadmium from Soil

Research Progress on Physical and Chemical Remediation Methods for the Removal of Cadmium from Soil

Diagnostic Ratios and Ecological Risk of Non-carcinogenic Polycyclic Aromatic Hydrocarcarbons (ncPAHs) in Egi Crude Oil Communities, Nigeria

The loadings of PAHs, its diagnostic ratios and ncPAHs at three cluster communities in Egi sub district of Niger-Delta with geographic coordinates of latitude 150 32ʹ 50ʺ N and longitude 60 34ʹ 42ʺ E were ascertained using Gas Chromatography (GC-FID, HP 5890 Series). The diagnostic ratios showed that Obagi had an LMW/HMW ratio of 0.2340, Ibewa's was 0.2222, and Obite's was 0.2549. In Obagi, the proportion of Low Molecular Weight (LMW) PAHs compared to High Molecular Weight (HMW) PAHs was 19%, while in Obite it was 18%, and in the Ibewa cluster it was 20%. The sediments of the Obagi, Obite, and Ibewa cluster sites exhibited a significant abundance of PAHs derived from pyrogenic sources, as evidenced by the presence of LMW/HWM ratios below 1. The identified ncPAHs include: Naphthalene, Acenaphthene, Acenaphthylene, Fluorene, Anthracene, Phenanthrene, Fluoranthene, Pyrene and Benzo(ghi)perylene. According to the results obtained the Obite cluster area exhibited the lowest concentrations (1.503mg/Kg) amongst the ncPAHs, while the Obagi study zone demonstrated the highest concentrations (1.5733mg/Kg). Among the nc(PAHs) examined, benzo (g,h,i) perylene exhibited the highest concentrations (2.086mg/Kg) across all locations, whereas acenaphthylene displayed the lowest concentration (0.123mg/kg) across the three cluster areas. However, none of the three study locations had any ncPAHs that are above the maximum permissible limit. Results from the application of risk quotient models (RQNCs and RQMPCs) to assess the ecological risk of ncPAHs as presented indicated that all the sites where these rivers' sediments were tested had RQNCs values for specific ncPAHs below 1, implying that these ncPAHs pose little or no danger to ecosystems. Also, the RQMPC score is less than 1, it means that the contamination from individual ncPAHs chemicals do not necessitate immediate remediation. Because the RQNCs and RQMPCs for a single PAH molecule are both less than 1, the contamination it generates might be considered low risk. Thus, few measures of control or correction would be required. The ecological risk of non-carcinogenic PAHs using RQMPCs and RQNCs indicated a very negligible risk which could be due to factors like heavy flooding that washed away soil surfaces. Application of Detoxification by chemical reaction technology should be used as future remediation method if there is need.

Nanomaterial-mediated strategies for enhancing bioremediation of polycyclic aromatic hydrocarbons: A systematic review

Polycyclic aromatic hydrocarbons (PAHs) are pervasive organic pollutants in the environment that are formed as an outcome of partial combustion of organic matter. PAHs pose a significant threat to ecological systems and human health due to their cytotoxic and genotoxic effects. Therefore, an immediate need for effective PAH remediation methods is crucial. Although nanomaterials are effective for remediation of PAHs, concerns regarding environmental compatibility and sustainability remains. Therefore, this study emphasizes integration of nanomaterials with bioremediation methods, which might offer a more sustainable and ecofriendly approach to PAHs remediation. A systematic search was conducted through scholarly databases from 2013 to 2023. A total of 360 articles were scrutinized, among which 26 articles were selected that resonated with the application of nano-bioremediation. These literatures comprise both comparative analysis of bioremediation only as well as nano-bioremediation. There is an elevation of 18.9 % in PAHs removal of liquid-phase samples, when comparing bioremediation (52.2 %) with nano-bioremediation (71.1 %). A consistent trend was observed in soil samples, with bioremediation and nano-bioremediation that successfully remove PAHs, with 60.8 % and 75.1 % respectively, indicating a 14.3 % improvement. Furthermore, the review elaborated on the various features of nanomaterials that led to their efficiency in the bioremediation of PAH. The review also discussed the strategies of nano-bioremediation namely nanomaterial-assisted microbial degradation, nanomaterial-assisted enzyme-enhanced microbial activity, nanomaterial-immobilized microbial cells, nanomaterial-facilitated electron transfer, and even some eco-green approaches to remediate PAHs, like biogenic nanomaterial for PAHs.

Enhanced Remediation of Phenanthrene and Naphthalene by Corn-Bacterial Consortium in Contaminated Soil.

The persistent and hazardous nature of polycyclic aromatic hydrocarbons (PAHs) released into the soil has become a critical global concern, contributing to environmental pollution. In this study, the removal efficiency of phenanthrene and naphthalene degradation by complex flora or pure bacteria combined with corn and their effects on the growth of corn, pH, and the number of soil bacteria were investigated using a pot experiment. The results indicate that the corn remediation method (P) outperformed degrading bacteria remediation (B) for phenanthrene, yet the combination (PB) exhibited significantly higher removal efficiency. The degradation efficiency of PB methods increased over time, ranging from 58.40% to 75.13% after 30 days. Naphthalene removal showed a similar trend. Soil pH, influenced by remediation methods, experienced slight but non-significant increases. The number of degrading bacteria increased with combined methods, notably with PB-W1 and PB-W2 treatments. Corn accumulated phenanthrene and naphthalene, with higher concentrations in roots. Remediation by the combined corn and degrading bacteria slightly increased PAH accumulation, indicating potential root protection. Biomass yield analysis revealed the inhibitory effects of PAHs on corn growth, decreased by degrading bacteria. PB-W1 and PB-EF3 demonstrated the highest fresh weight and moisture content for stem and leaf biomass, while PB-F2-6 excelled in root biomass. Overall, combined remediation methods proved more effective, which underscores the potential of the corn and degrading bacteria consortium for efficient PAH remediation in contaminated soil.

Assessment results of sites impacted by accumulated environmental damage along the coastline of the Barents Sea (Eastern Murman)

The article discusses the findings from monitoring sites of accumulated environmental damage (AED) along the East Murman coastline. The area surveyed includes the mouth of the Kharlovka River estuary, which is near the Seven Islands Archipelago within the Kandalaksha State Nature Reserve. During a thorough engineering and environmental assessment of the region, an inventory of AED sites was conducted, along with an evaluation of the amount of accumulated waste and an analysis of pollutant levels in the soil. The survey revealed six unauthorized waste disposal sites, primarily consisting of fuel and lubricant containers and scrap metal. Soil testing at two locations within the Barents Sea’s water protection zone indicated significant contamination with oil products, while the levels of metals (Zn, Cd, Pb, Cu) were found to be acceptable. The analysis of soil conditions revealed that degradation within the Kharlovka River estuary began during the operation of a fuel and lubricants storage facility in the area. At the time of the assessment, over a third of the surveyed area lacked a fertile soil layer, and the remaining soil and vegetation were sparse. The degree of contamination by oil products requires the implementation of highly efficient soil remediation methods.

Microbially Induced Calcium Carbonate Precipitation UsingLysinibacillussp.: A Ureolytic Bacteriumfrom Uttarakhand for Soil Stabilization.

Microbially induced calcium carbonate precipitation (MICP) is a soil remediation method that has emerged as a viable and long-term solution for enhancing soil mechanical qualities. The technique of MICP that has been extensively researched is urea hydrolysis, which occurs naturally in the environment by urease-producing bacteria as part of their fundamental metabolic processes. The objectives of the current study include screening and identifying native ureolytic bacteria from soil in Uttarakhand, optimizing growth factors for increased urease activity, and calcite precipitation by the bacteria using response surface methodology. Additionally, it was assessed how well the isolated bacteria in the medium biomineralized when using synthetic media and cheaper alternatives such as cow urine and eggshell as sources of urea and Ca2+, respectively. The isolated strain identified as Lysinibacillus sp. was found to be the very active strain after soil samples were screened for ureolytic bacteria. It was discovered that optimization studies with values of pH 8, urea concentration (0.8M), inoculum concentration (3%), and incubation time (48h) yielded a higher activity of 33.7 U/mL (threefold increase), and a higher calcium carbonate precipitation (enzyme activity: 10.96 U/mL, pH: 8.92, soluble Ca2⁺: 25.53mM and insoluble Ca2⁺: 0.856g). The calcite precipitation in broth media supplemented with ready-made substrates and alternative sources demonstrated a similar result of increased pH and ammonia release. Thus, the current study successfully paves the way for several possibilities to stabilize the slopy soils prone to landslides and erosion in Uttarakhand and pinpoint an economic approach through biomineralization.

A Critical Review on the Factors Affecting the Bond Strength of Direct Restorative Material Alternatives to Amalgam.

This article comprehensively reviews the performance of simplified direct restorative materials that have the potential to be an alternative to amalgam. Following an understanding of the material structures and clinical performances, this review provides an analysis of the bonding mechanisms and influential factors on the bond strength. These factors include substrate-related variations, involving primary vs. permanent dentin, sound- vs. caries-affected/demineralized dentin comparisons and surface-related factors and pretreatments. Special attention is given to the factors changing the substrate surface, such as different contaminants, remedy methods after contamination and different conditioning methods related to the materials. Variations in sample preparation and bond strength test parameters are also evaluated for the analysis of the outcomes. This review aims to provide an overview of the factors involved in the application procedure of direct restorations together with in vitro testing variations to guide the selection of suitable materials by understanding strengths and shortcomings.

Unexpected increase in microalgal removal of doxylamine induced by bicarbonate addition: synergistic chem-/bio-degradation mechanisms

Microalgae-based approaches serves as promising methods for remediation of pharmaceutical contaminants (PCs) compare to conventional wastewater treatment processes. However, how to decrease hydraulic retention times of the microalgal system currently has been one of the main bottlenecks. This study constructed an unexpected synergistic extra-chem-/intra-bio-degradation system by addition of 5.95 mM bicarbonate in the microalgal system, which achieved complete removal (100%) of a representative PC, doxylamine (DOX) in 96 h compare to that 192 h in the control. Removal capacities and mass balance analyses demonstrated that biodegradation rate per unit microalgal density was significantly increased by 207%. Further analyses using transcriptomic, enzymatic inhibitory test, and high-resolution mass spectrometry revealed that after addition of bicarbonate for metabolism of DOX, a hydrolase (CYP97C1) and a primary amine oxidase (TynA) can catalyze DOX into doxylamine N-oxide and an intermediate (C15H17NO2) with a m/z of 244.1335. Meanwhile, bicarbonate reacted with microalgae-excreted hydrogen peroxide to form more oxidative radicals including superoxide and hydroxyl radicals extracellularly, which promised the extracellular degradation of DOX according to the oxidative radical inhibiting tests. Further investigation showed addition of bicarbonate in microalgal system improved the removal rate of 17 PCs by up to 500.8%. Therefore, this study not only developed an approach to enhance treatment efficiencies of diverse PCs by microalgae within a shorter time, but also carried unique mechanistic insights into the underlying principles.

Optimization of Ecofriendly L-Fe/Ni Nanoparticles prepared using extract of black tea leaves for Removal of tetracycline antibiotics from Groundwater by Response Surface Methodology

This article focuses on employment of nanotechnologies in remediation of tetracycline antibiotics (TC) from groundwater by green synthesized bimetallic Fe/Ni supported by limestone particles. An in-situ green synthesis nanoparticles was prepared using black tea leaves extract to generate a L-Fe/Ni nanocomposite. The synthesized nanocomposite was characterized using several techniques, such as, X-Ray Diffraction (XRD), Scanning Electron microscopy (SEM), transmission electron microscope (TEM), Energy dispersive X-ray (EDX), FTIR (Fourier Transform-Infra Red) spectroscopy and surface area. We then use response surface methodology (RSM) to optimize the synthesis process and evaluate the effectiveness of the prepared nanocomposite for tetracycline remediation. We took different simulated concentrations of the TC contaminant without relying on actual TC concentrations in grounwater, the best removal of the TC contaminant in batch study was investigated with relying on the initial concentrations of TC and other experimental factors such as pH, adsorbent nanomaterial concentration and time. A pilot plant was then constructed to eliminate the TC contaminant from groundwater in different concentrations, where the removal efficiency was found decreased with increasing in the concentration of the TC Many parameters affecting the removal mechanisms in statistical and continuous systems were examined to select the best results that accomplish the maximum elimination rate. With the improved operating conditions, (L-Fe/Ni concentration: 1500 mg/L; concentration of TC: 20 mg/L; pH: 7.2; contact time: 128 min), removal percent of TC was found 87 % based on RSM system. The L-Fe/Ni reactive medium of continuous column has a main role in slowing down the movement of the TC plume. This study showed that the ecofriendly nanocomposite could be an appropriate and novel method for remediation of antibiotics and other contaminants in groundwater.

Multifunctional aluminum 12-hydroxystearate/lignin polyurethane foam for selective gelation and efficient separation of oil and organic solvents

During frequent transportation, the marine environment is continuously exposed to significant threats from crude oil and organic solvent leakage. Non-covalent self-assembly of organogelator on the adsorbent matrix to fix non-polar solvents is an efficient and sustainable remediation method. This contribution proposes an organogelator-adsorbent composite by blending aluminum 12-hydroxystearate (Al HSA) and expanded graphite (EG) during lignin-based polyurethane foaming. Al HSA molecule synergizes with EG to modulate the shape (hexagonal), oil retention, mechanical property, and hydrophobicity (water contact angle = 151.3°) of the lignin-based polyurethane foam (LPUF) skeleton. Al HSA-LPUF (OTS-LPUF/EAH) superhydrophobic foam exhibits sorption capacity up to 13.2–53.0 g g−1 in various oils and organic solvents. From the microscopic morphology, the Al HSA on the skeleton self-assembles into spherical nanoclusters driven by hydrogen bonding, realizing the capturing of oils and organic solvents. Even after 20 cycles, the foam still has a high oil/water separation capacity and mechanical performance. OTS-LPUF/EAH also shows improved flame retardancy and a 61 % reduction in total smoke release (TSR) compared to pristine LPUF.

Efficacy of P-sorbent material combined with aquatic plants in controlling nutrient release from urban lake sediment: Field investigation

The release of stored nutrients from sediments is thought to substantially affect water quality in urban lakes. To explore the efficiency of different in-situ remediation methods on controlling high internal urban lake sediments, 120 days of field-enclosure experiments were conducted to investigate the efficacy of P-sorbent materials combined with aquatic plants in controlling nutrient release from urban-lake sediments. The lanthanum-modified clay (LMC) effectively reduced sediment P release flux and could temporarily lead to a small increase in N concentration in the overlying water. In contrast, Vallisneria spiralis (V. spiralis) has a relatively weak effect on controlling nutrient release and can even cause an increase in P concentration. The combined restoration technique of V. spiralis + LMC can overcome the drawbacks of a single method, reduce the nutrient content in overlying water, and inhibit the sediment internal release. Relative to the control, the V. spiralis + LMC treatment reduced mobile P content by 52.5% and increased Ca-P content by 34.5%. The added lanthanum contained material can quickly bind the readily released P in sediment and porewater, transforming it into intert P over time. Submerged macrophytes can absorb active P in water and sediments and transport oxygen to sediments promoting denitrification and N removal. The combined restoration technique synergistically combines the high P sorption affinity of LMC and the substrate improvement effect of V. spiralis, thus realizing the long-term control of endogenous release in urban lakes. This approach holds great promise for restoring urban lakes with high endogenous nutrient loading.

Efficient visible-light-driven photocatalytic degradation of indoor formaldehyde using an indium-based MOF/graphene oxide composite

Formaldehyde (HCHO) severely degrades indoor air quality, and conventional remediation methods are often inadequate for addressing low concentrations of HCHO indoors. In this study, we synthesized a MIL-68(In)-NH2/graphene oxide (GO) composite using a solvothermal method, aimed specifically at enhancing the photocatalytic degradation of HCHO under visible light. Our results show that the integration of GO enhances visible light absorption and facilitates efficient electron transport, significantly improving photocatalytic performance. The MIL-68(In)-NH2/GO composite achieves a 77 % degradation rate of HCHO, significantly outperforming MIL-68(In)-NH2 (51 %) and GO (22 %) alone. This enhanced activity is attributed to the effective separation of electron-hole pairs and synergistic interactions within the composite. We proposed an enhanced photocatalytic mechanism for the MIL-68(In)-NH2/GO system, identifying h+ and •O2– as the principal active species. Moreover, the MIL-68(In)-NH2/GO composite shows excellent reusability and stability, making it a promising candidate for eco-friendly and efficient indoor air purification using metal–organic frameworks.

Synergistic Release of Cd(II) and As(V) from Ternary Sorption Systems Containing Ferrihydrite Nanoparticles: The Role of Binary and Ternary Surface Complexes

Cadmium (Cd) and arsenic (As) generally exhibit mutually beneficial co-sorption behavior on iron oxyhydroxides through multiple mechanisms, including surface precipitation, ternary surface complexes, and electrostatic interactions. However, the numerous factors that control the immobilization of Cd and As in turn complicated the processes and mechanisms involved in their co-desorption from iron minerals, which hindered the full understanding of their geochemical behaviors. Here, the simultaneous release of Cd(II) and As(V) from newly precipitated ferrihydrite nanoparticles by either Ca or P was investigated through kinetics and isothermal desorption experiments. We showed that the Cd(II) and As(V) present two-phase desorption processes (rapid desorption and slow desorption) in both binary (Fe-Cd or Fe-As alone) and ternary systems (Fe-Cd-As co-presence). Compared to their binary counterparts, Cd(II) and As(V) in the ternary systems are more prone to detachment from ferrihydrite. Further desorption of Cd(II) and As(V) at different co-presence scenarios (different initial concentrations) demonstrated mutual promotion behaviour towards their counterparts; the co-presence of Cd(II) facilitates the desorption of As(V), while the co-presence of As(V) also promotes the desorption of Cd(II). XPS and FTIR results demonstrated that either Ca or P showed minor effects on the binding environment of Cd and As. Further results from the in-situ ATR-FTIR experiment and second derivative peak fitting analysis indicate that the enhanced detachment of Cd(II) and As(V) from the ternary system may be due to the synergistic desorption of the ternary surface complexes and other surface complex species. Our results provide new insights into the prediction of the environmental behaviour of the coexistence of Cd(II) and As(V) in iron-rich geological settings. The potential environmental risks of iron-based remediation methods should be considered due to the enhanced bioavailability of Cd(II) and As(V) in co-presence circumstances.

Enhanced adsorption of aqueous perfluorooctanoic acid on iron-functionalized biochar: Elucidating the roles of inner-sphere complexation

Perfluorooctanoic acid (PFOA) is ubiquitously detected in various water bodies, which raises the urgent need for developing effective and economic remediation methods in response to its health risks. The adsorptive removal of PFOA by biochar (BC) is regarded as a simple, effective, and economical technique. However, engineered BCs, including FeCl3-activated BC, for PFOA removal and adsorption mechanisms have been ill-studied. In this study, a FeCl3-activated dairy manure-derived biochar (Fe@MBC) was prepared via one-step pyrolysis/activation, and its properties and adsorption characteristics were compared with a pristine manure-derived biochar (P-MBC). The FeCl3 activation largely increased the surface area of Fe@MBC and the deposition of FexOy minerals on surface of Fe@MBC while significantly elevating the surface roughness of Fe@MBC. The maximum adsorption capacity of Fe@MBC for PFOA (233 mg·g−1) was five times higher than that of P-MBC (46 mg·g−1). PFOA adsorption was favorable at low solution pH and was independent on ionic strength, which supported the major contribution by inner-sphere complexation rather than out-sphere complexation. This mechanism was further confirmed by the disappearance of FeO peak on Fourier transform infrared spectrum and the blue-shift of Fe binding energies on X-ray photoelectron Fe 2p spectrum of Fe@MBC after PFOA adsorption. Fe@MBC maintained a near 100 % adsorption capacity for PFOA after 3 cycles of chemical regeneration. Fe@MBC also exhibited efficient removal for PFOA and other PFAS compounds at trace levels in the lake water and dairy effluent. Thus, this study highlights a promising insight for selectively eliminating PFASs from water.

N vacancies and OH/C=O co-modified g-C3N4 photoactivated peroxymonosulfate for the degradation of tetracycline: Synergistic promotion effect between excitons and carriers

Activation of peroxymonosulfate (PMS) to generate reactive oxygen species (ROS) for pollutant degradation via metal-free photocatalysts is an important green wastewater treatment and remediation method, but the pathway for generating ROS via exciton effects in catalysts is often overlooked. In this study, OH/C=O co-modified N-defective rod-shaped carbon nitride (Nv-CN-O) was designed and synthesized by soft template and alkali hydrothermal method. In the Nv-CN-O/PMS/Light system, there was a synergistic degradation of tetracycline (TC) by carriers and excitons, with a degradation rate 2.15 times higher than that of CN/PMS/Light. N vacancies and OH/C=O enhanced the adsorption to PMS, accelerated the charge transfer process, and activated PMS to generate ·O2− dominated reactive species. The functional group OH/C=O promoted the production of triplet excitons that through the energy transfer pathway to promote the production of 1O2. Abundant ROS were involved in the TC degradation process, and three possible TC degradation pathways were proposed. Nv-CN-O has strong anti-interference ability in actual water bodies, shows a promoting effect on the degradation of TC, which has practical application potential.

Mechanobiological mechanisms in the remediation of soil lead pollution using two-dimensional carbon materials and Morchella: A molecular-level study

Graphene-based 2D carbon composites and Morchella mushrooms are used in the paper to study the mechanobiological mechanisms of soil lead remediation. Soil is contaminated with lead, which threatens ecosystems and human health, making it even more important to find remedies. To fully comprehend these processes, present-day materials, and organic compounds are needed to improve soil nutrition and eradicate lead. To deal with the challenge of finding effective means of lead removal; limitations associated with traditional soil pollution remediation methods; and merging biology and material sciences. Multifunctional graphene wettability-patterned nanocoated membranes (MGW-PNM) is a novel technique developed to overcome these challenges. Such processes result in membranes with different wettability patterns that take advantage of the properties of graphene. This facilitates better interaction between the membrane itself and the surrounding soil as well as lead contaminants by modifying its hydrophobicity or hydrophilicity characteristics. For effective removal of lead, extensive simulation studies were done using MGW-PNM. In line with this, it can be inferred that MGW-PNM also remediates highly capable soils at high-efficiency levels. This was established when comparing modern techniques to past ones where considerable improvements were made on how much lead is extracted from them. The study suggests new ways of addressing environmental contamination resulting from microbial activities in soils by combining advanced materials with biological substances such as Morchella spp. For this purpose, it investigates various molecular interactions occurring among carbonaceous species called Morchella microbes and environmental pollutants like those including Pb.

PFAS: The Journey from Wonder Chemicals to Environmental Nightmares and the Search for Solutions

Per- and polyfluoroalkyl substances (PFAS) are diverse synthetic chemicals manufactured over seven decades. It is an aliphatic molecule with a basic hydrophobic structure of carbon and fluorine linked to a hydrophilic end group. Due to their physicochemical properties associated with the unique structure, PFAS has been used in a wide variety of applications including aqueous film-forming foams (AFFF), paper, carpets, non-stick cookware, etc. as they make products resistant to water, heat, and stains. These molecules have drawn great attention recently for their unique properties, high stability and low degradability, and so-called “Forever Chemicals”. PFAS has the strongest carbon-fluorine bond which makes them persistent in the environment. Hence it contaminates natural resources and endangers public health. This review discusses the discovery, development, and evolution of PFAS from the wonder chemical era to a nightmare chemical era, exposure and its impacts on human health and the environment, current remediation techniques, and future trends of PFAS molecules and related products. The primary objective of this review is to identify knowledge gaps on PFAS contamination, remediation methods, and possible PFAS alternatives.