Recent Progress on Synthesis and Properties of Black Phosphorus and Phosphorene As New-Age Nanomaterials for Water Decontamination.

Concerted efforts have been made in recent years to find solutions to water and wastewater treatment challenges and eliminate the difficulties associated with treatment methods. Various techniques are used to ensure the recycling and reuse of water resources. Owing to their excellent chemical, physical, and biological properties, nanomaterials play an important role when integrated into water/wastewater treatment technologies. Black phosphorus (BP) is a potential nanomaterial candidate for water and wastewater treatment, especially its monolayer 2D derivative called phosphorene. Phosphorene offers relative adjustability in its direct bandgap, high charge carrier mobility, and improved in-plane anisotropy compared to the most extensively studied 2D nanomaterials. In this study, we examined the physical and chemical characteristics and synthetic processes of BP and phosphorene. We provide an overview of the latest advancements in the main applications of BP and phosphorene in water/wastewater treatment, which are categorized as photocatalytic, adsorption, and membrane filtration processes. Additionally, we explore the existing difficulties in the integration of BP and phosphorene into water/wastewater treatment technologies and prospects for future research in this field. In summary, this review highlights the ongoing necessity for significant research efforts on the integration of BP and phosphorene in water and wastewater applications.

Cerium-Doped CuFe-Layered Catalyst for the Enhanced Oxidation of o-Xylene and N,N-Dimethylacetamide: Insights into the Effects of Temperature and Space Velocity.

Volatile organic compounds (VOCs) are among the most potential pollutant groups that cause air quality degradation because of their toxic effects on human health. Although catalytic oxidation is an effective method for VOC removal, further studies are required to develop more efficient and affordable catalysts. In this study, cerium (Ce) was doped into a CuFe-layered material (Ce-CuFe) to improve the catalytic oxidation efficiencies of N,N-dimethylacetamide (DMAC) and o-xylene. The synthesized catalyst was characterized using X-ray diffraction (XRD), scanning electron microscopy (SEM), high-resolution transmission electron microscopy (HR-TEM), energy-dispersive X-ray spectroscopy (EDS), Fourier-transform infrared spectroscopy (FTIR), and X-ray photoelectron spectroscopy (XPS) analysis. XRD analysis confirmed the successful doping of Ce atoms into the CuFe-layered structure, while in the SEM and TEM images the catalyst appeared as uniformly distributed two-dimensional plate-like particles. The catalytic oxidation performance of the Ce-CuFe was investigated at six temperatures between 200 and 450 °C and three space velocities in the range of 31000-155000 mLh-1g-1 for the oxidation of DMAC and o-xylene, which functioned as polar and nonpolar solvents, respectively. At 200 °C, the Ce-CuFe catalyst performed 50% greater when oxidizing o-xylene while exhibiting a DMAC oxidation efficiency that was 42% greater than that achieved using undoped CuFe. The Ce-CuFe could remove DMAC and o-xylene with an efficiency higher than 95% at 450 °C. Furthermore, Ce-doped CuFe exhibited high resistance against moisture and outstanding reusability performance with only a 5.6% efficiency loss after nine reuse cycles. Overall, the incorporation of Ce into a CuFe-layered material is a promising strategy for the oxidation of various VOCs.

Enhanced generation of reactive radicals and electrocatalytic oxidation of levofloxacin using a trimetallic CuFeV layered double hydroxide-containing electrode.

In Electro-Fenton (EF) processes, the use of iron as a catalyst under acidic conditions results in increased costs and potential secondary pollution. To address these issues, we developed a CuFeV layered double hydroxide (LDH) coating on graphite felt (GF) (CuFeV LDH@GF) that offers an effective performance across a broad pH range without causing metal pollution. The CuFeV LDH@GF cathode exhibited a good oxygen reduction performance, high stability, and an efficient removal of levofloxacin (LEV) over a wide pH range (pH = 3-10). The simultaneous presence of Cu2+/Cu3+, Fe2+/Fe3+, and V4+/V5+ redox pairs played a crucial role in facilitating interfacial electron transfer, thereby enhancing the production and subsequent activation of H2O2 within the system. The apparent rate constant (kapp) of LEV removal under neutral conditions with the CuFeV LDH@GF electrode was more than twice that of the raw GF electrode. This improvement can be attributed to the CuFeV LDH coating, which increased the generation of hydroxyl radicals (•OH) from 0.64 to 1.27 mM. Importantly, the CuFeV LDH@GF electrode maintained its efficiency and stability even after 10 reuse cycles. Additionally, GC-MS analyses revealed the degradation of intermediate compounds, which included cyclic and aliphatic compounds. This study provides significant insights into the synergistic effects of trimetallic LDHs, contributing to the development of high-performance cathodes.

Evaluation of vertical distribution characteristics of microplastics under 20 µm in lake and river waters in South Korea.

Following the alarming reports of microplastic pollution in the marine environment, increased attention has been given to microplastics in other environmental media. Despite the attention, there is limited research available on the depth-distribution of microplastics in freshwater. Specifically, in the case of water sources used for drinking or tap, the height of intake facilities varies, and it is highly likely that there is a correlation between the vertical distribution of microplastics and these water intake structures. Further, because the size of microplastics varies widely in the environment, the commonly used sampling devices are not suitable for selectively extracting microplastics without causing cross-contamination. Thus, we developed a suitable device for microplastics of size 5-20 µm and studied microplastic distribution in freshwater at various depths by considering various types of microplastics and aqueous systems. Lake and river, two major water sources, were selected for the study of microplastics distribution in water system. The microplastic distribution characteristics in both water systems showed that polypropylene and polyethylene were the most abundant across all depths because of their production volume. Plastic types with higher density were found only at the lower layers, and polystyrene was found in the upper layers because of the environmental effects on its buoyancy caused pore diameter and surface area. The lake and river had higher microplastic distribution in the lower layer and upper layer, respectively. This was because the flow rate in river was higher than that of lake. The higher flow rate reduced the settling velocity in river. Thus, hydrodynamic stability influences the vertical distribution and concentrations of microplastics in the water systems. These results are expected to be used for understanding the behavioral characteristics of microplastics in water systems and to manage water sources.

Ultrasonic-assisted photocatalytic degradation of various organic contaminants using ZnO supported on a natural polymer of sporopollenin.

Water resource pollution by organic contaminants is an environmental issue of increasing concern. Here, sporopollenin/zinc oxide (SP/ZnO) was used as an environmentally friendly and durable catalyst for sonophotocatalytic treatment of three organic compounds: direct blue 25 (DB 25), levofloxacin (LEV), and dimethylphtalate (DMPh). The resulting catalyst had a 2.65 eV bandgap value and 9.81 m2/g surface area. The crystalline structure and functional groups of SP/ZnO were confirmed by X-ray diffraction (XRD) and Fourier transforms infrared spectroscopy (FTIR) analyses. After 120 min of the sonophotocatalysis, the degradation efficiencies of DB 25, LEV, and DMPh by SP/ZnO were 86.41, 75.88, and 62.54%, respectively, which were higher than that of the other investigated processes. The role of reactive oxygen species were investigated using various scavengers, enhancers, photoluminescence, and o-phenylenediamine. Owing to its stability, the catalyst exhibited good reusability after four consecutive cycles. In addition, the high integrity of the catalyst was confirmed by scanning electron microscopy (SEM), XRD, and FTIR analyses. After four consecutive examinations, the leaching of zinc in the aqueous phase was < 3 mg/L. Moreover, gas chromatography-mass spectrometry (GC-MS) analyses indicated that the contaminants were initially converted into cyclic compounds and then into aliphatic compounds, including carboxylic acids and animated products. Thus, this study synthesized an environmentally friendly and reusable SP/ZnO composite for the degradation of various organic pollutants using a sonophotocatalytic process.

Microplastics in water systems: A review of their impacts on the environment and their potential hazards.

Microplastics, the microscopic plastics, are fragments of any type of plastic that are being produced today as plastic waste originating from anthropogenic activities. Such microplastics are discharged into the environment, and they enter back into the human body through different means. The microplastics spread in the environment due to environmental factors and the inherent properties of microplastics, such as density, hydrophobicity, and recalcitrance, and then eventually enter the water environment. In this study, to better understand the behavior of microplastics in the water environment, an extensive literature review was conducted on the occurrence of microplastics in aquatic environments categorized by seawater, wastewater, and freshwater. We summarized the abundance and distribution of microplastics in the water environment and studied the environmental factors affecting them in detail. In addition, focusing on the sampling and pretreatment processes that can limit the analysis results of microplastics, we discussed in depth the sampling methods, density separation, and organic matter digestion methods for each water environment. Finally, the potential hazards posed by the behavior of aging microplastics, such as adsorption of pollutants or ingestion by aquatic organisms, due to exposure to the environment were also investigated.

Insights into engineered graphitic carbon nitride quantum dots for hazardous contaminants degradation in wastewater.

Increased environmental pollution is a critical issue that must be addressed. Photocatalytic, adsorption, and membrane filtration methods are suitable in environmental governance because of their high selectivity, low cost, environment-friendly nature, and excellent treatment efficiency. Graphitic carbon nitride (g-C3N4) quantum dots (QDs) have been considered as photocatalysts, adsorbents, and membrane materials for wastewater treatments, owing to their stability, adsorption capacity, photochemical properties, and low toxicity and cost. This review summarizes g-C3N4 QD synthesis techniques, operating parameters affecting the removal performance in the treatment process, modification effects with other semiconductors, and benefits and drawbacks of g-C3N4 QD-based materials. Furthermore, this review discusses the practical applications of g-C3N4 QDs as adsorbents, photocatalysts, and membrane materials for organic and inorganic contaminant treatments and their value-added product formation potential. Modified g-C3N4 QD-based material adsorbents, photocatalysts, and membranes present potentially applicable effects, such as removal of most waterborne contaminants. Excellent results were obtained for the reduction of methyl orange, bisphenol A, tetracycline, ciprofloxacin, phenol, rhodamine B, E. coli, and Hg. Overall, this paper provides comprehensive background on g-C3N4 QD-based materials and their diverse applications in wastewater treatment, and it presents a foundation for the enhancement of similar unique materials in the future.

Catalytic activation of hydrogen peroxide by Cr2AlC MAX phase under ultrasound waves for a treatment of water contaminated with organic pollutants.

This study aims to investigate the sonocatalytic activation of hydrogen peroxide (H2O2) using Cr2AlC MAX phase prepared by the reactive sintering process. The hexagonal structure of the crystalline MAX phase was confirmed by X-ray diffraction. Moreover, the compacted layered structure of the MAX phase was observed via scanning electron microscopy and high-resolution transmission electron microscopy. Under the desired operating conditions, Cr2AlC MAX phase (0.75 g/L) showed suitable potential to activate H2O2 (1 mmol/L) under sonication, thereby allowing a considerable removal efficiency for various organic pollutants, including dimethyl phthalate (69.1%), rifampin (94.5%), hydroxychloroquine (100%), and acid blue 7 (91.5%) with initial concentration of 15 mg/L within 120 min of treatment. Kinetic analysis proved that the degradation reaction followed pseudo-first-order kinetics. Scavenging tests demonstrated that hydroxyl radicals and singlet oxygen were effective species during degradation. Furthermore, a probable mechanism for dimethyl phthalate degradation was suggested according to gas chromatography-mass spectroscopy and nuclear magnetic resonance analyses. The obtained results confirmed the capability of the triple Cr2AlC/H2O2/US process as a promising method for treating contaminated water.

Titanium-based MAX-phase with sonocatalytic activity for degradation of oxytetracycline antibiotic.

In light of growing environmental concerns over emerging contaminants in aquatic environments, antibiotics in particular, have prompted the development of a new generation of effective sonocatalytic systems. In this study, a new type of nano-laminated material, Ti2SnC MAX phase, is prepared, characterized, and evaluated for the sonocatalytic degradation of oxytetracycline (OTC) antibiotic. A variety of identification analyses, including X-ray diffraction, scanning electron microscopy, energy-dispersive X-ray spectrometry, Brunauer-Emmett-Teller, and diffuse reflectance spectroscopy, were conducted to determine the physicochemical properties of the synthesized catalyst. By optimizing the operating factors, total degradation of OTC occurs within 120 min with 1 g L-1 catalyst, 10 mg L-1 OTC, at natural pH of 7.1 and 150 W ultrasonic power. The scavenger studies conclude that the singlet oxygen and superoxide ions are the most active species during the sonocatalytic reaction. Based on the obtained data and GC-MS analysis, a possible sonocatalytic mechanism for the OTC degradation in the presence of Ti2SnC is proposed. The catalyst reusability within eight consecutive runs reveals the proper stability of Ti2SnC MAX phase. The results indicate the prospect for MAX phase-based materials to be developed as efficient sonocatalysts in the treatment of antibiotics, suggesting a bright future for the field.

Direct and selective determination of p-coumaric acid in food samples via layered Nb4AlC3-MAX phase.

Phenolic compounds that are naturally found in food samples are not only an important part of the human diet but also useful bioactive substances for health. Among these, para-coumaric acid (p-CA) has antibacterial and antioxidant properties and is used in many industrial processes. In this study, the novel MAX-phase material, Nb4AlC3, was successfully prepared and characterized in detail with various spectroscopic, microscopic and thermal techniques. The sensor performance of Nb4AlC3 modified glassy carbon electrode (Nb4AlC3@GCE) was evaluated and analytical parameters were calculated. Experimental conditions such as pH and amount of modifier were optimized with differential pulse voltammetry (DPV) measurements. The real samples analyses of lemon, apple and pomegranate were applied for determination of p-CA with Nb4AlC3@GCE sensing system under the optimized conditions. The accuracy was evaluated by spike/recovery and high-performance liquid chromatography analysis, which accounted for high accuracy of the Nb4AlC3@GCE sensing system. The limit of detection, limit of quantification, linear working range and relative standard deviation (%) of the Nb4AlC3@GCE sensing system were determined as 0.28 and 0.85 µmol/L, 0.8-80.0 µmol/L, 3.17 %, respectively. The results showed that the proposed sensing system has the high precision at lower concentration of p-CA.

Treatment of Water Contaminated with Non-Steroidal Anti-Inflammatory Drugs Using Peroxymonosulfate Activated by Calcined Melamine@magnetite Nanoparticles Encapsulated into a Polymeric Matrix.

In the present study, calcined melamine (CM) and magnetite nanoparticles (MNPs) were encapsulated in a calcium alginate (CA) matrix to effectively activate peroxymonosulfate (PMS) and generate free radical species for the degradation of ibuprofen (IBP) drug. According to the Langmuir isotherm model, the adsorption capacities of the as-prepared microcapsules and their components were insignificant. The CM/MNPs/CA/PMS process caused the maximum degradation of IBP (62.4%) in 30 min, with a synergy factor of 5.24. Increasing the PMS concentration from 1 to 2 mM improved the degradation efficiency from 62.4 to 68.0%, respectively, while an increase to 3 mM caused a negligible effect on the reactor effectiveness. The process performance was enhanced by ultrasound (77.6% in 30 min), UV irradiation (91.6% in 30 min), and electrochemical process (100% in 20 min). The roles of O•H and SO4•- in the decomposition of IBP by the CM/MNPs/CA/PMS process were 28.0 and 25.4%, respectively. No more than 8% reduction in the degradation efficiency of IBP was observed after four experimental runs, accompanied by negligible leachate of microcapsule components. The bio-assessment results showed a notable reduction in the bio-toxicity during the treatment process based on the specific oxygen uptake rate (SOUR).

Peroxydisulfate-assisted sonocatalytic degradation of metribuzin by La-doped ZnFe layered double hydroxide.

Metribuzin is an herbicide that easily contaminates ground and surface water. Herein, La-doped ZnFe layered double hydroxide (LDH) was synthesized for the first time and used for the degradation of metribuzin via ultrasonic (US) assisted peroxydisulfate (PDS) activation. The synthesized LDH had a lamellar structure, an average thickness of 26 nm, and showed mesoporous characteristics, including specific surface area 110.93 m2 g-1, pore volume 0.27 cm3 g-1, and pore diameter 9.67 nm. The degradation efficiency of the US/La-doped ZnFe LDH/PDS process (79.1 %) was much greater than those of the sole processes, and the synergy factor was calculated as 3.73. The impact of the reactive species on the sonocatalytic process was evaluated using different scavengers. After four consecutive cycles, 10.8 % loss occurred in the sonocatalytic activity of the La-doped LDH. Moreover, the efficiency of the US/La-doped LDH/PDS process was studied with respect to the degradation of metribuzin in a wastewater matrix. According to GC-MS analysis, six by-products were detected during the degradation of metribuzin. Our results indicate that the US/La-doped ZnFe LDH/PDS process has great potential for efficient degradation of metribuzin-contaminated water and wastewater.

MOF-Based Mycotoxin Nanosensors for Food Quality and Safety Assessment through Electrochemical and Optical Methods.

Mycotoxins in food are hazardous for animal and human health, resulting in food waste and exacerbating the critical global food security situation. In addition, they affect commerce, particularly the incomes of rural farmers. The grave consequences of these contaminants require a comprehensive strategy for their elimination to preserve consumer safety and regulatory compliance. Therefore, developing a policy framework and control strategy for these contaminants is essential to improve food safety. In this context, sensing approaches based on metal-organic frameworks (MOF) offer a unique tool for the quick and effective detection of pathogenic microorganisms, heavy metals, prohibited food additives, persistent organic pollutants (POPs), toxins, veterinary medications, and pesticide residues. This review focuses on the rapid screening of MOF-based sensors to examine food safety by describing the main features and characteristics of MOF-based nanocomposites. In addition, the main prospects of MOF-based sensors are highlighted in this paper. MOF-based sensing approaches can be advantageous for assessing food safety owing to their mobility, affordability, dependability, sensitivity, and stability. We believe this report will assist readers in comprehending the impacts of food jeopardy exposure, the implications on health, and the usage of metal-organic frameworks for detecting and sensing nourishment risks.

Synthesis of visible light responsive ZnCoFe layered double hydroxide towards enhanced photocatalytic activity in water treatment.

In this study, a ternary layered double hydroxide containing Zn, Co, and Fe transition metals (ZnCoFe LDH) was developed using a co-precipitation procedure. The as-synthesized photocatalyst was evaluated for its performance in the degradation of methylene blue (MB) under visible light irradiation. The effects of various process conditions including photocatalyst dosage, pollutant concentration, pH, lamp distance, and lamp power were investigated. The ZnCoFe LDH achieved approximately 74% photodegradation efficiency owing to the narrow bandgap of 2.14 eV. The Langmuir-Hinselwood rate constants were calculated as 1.17 min-1 and 3.55 min-1 for photolysis by LED lamp alone and for photocatalysis by LED/ZnCoFe LDH, respectively. The photocatalytic ability of the LDH was attributed to the generation of radical species like •OH and O2•-. The photocatalytic degradation intermediates of MB were determined by GC-MS analysis. The catalyst retained its performance throughout seven reuse cycles with only a 4.17% reduction in removal efficiency. The energy per order EEO of the ZnCoFe/LED process in 180 min treatment time was determined as 5.41 kWh.m-3. order-1. This study shows that ZnCoFe LDH has sufficient activity and photostability for long-term application in photocatalytic water treatment.

Advances in layered double hydroxide based labels for signal amplification in ultrasensitive electrochemical and optical affinity biosensors of glucose.

Since the development of enzyme electrodes, the research area of glucose biosensing has seen outstanding progress and improvement. Numerous sensing platforms have been developed based on different immobilization techniques and improved electron transfer between the enzyme and electrode. Interestingly, these platforms have consistently used innovative nanostructures and nanocomposites. In recent years, layered double hydroxides (LDHs) have become key tools in the field of analytical chemistry owing to their outstanding features and benefits, such as facile synthesis, cost-effectiveness, substantial surface area, excellent catalytic performance, and biocompatibility. LDHs are often synthesized as nanomaterial composites or manufactured with specific three-dimensional structures. The purpose of this review is to illustrate the biosensing prospects of LDH-based glucose sensors and the need for improvement. First, various clinical and conventional approaches for glucose determination are discussed. The definitions, types, and various synthetic methodologies of LDHs are then explained. Subsequently, we discuss the various research studies regarding LDH-based electrochemical and optical assays, focusing on modified systems, improved electron transfers pathways (through developments in surface science), and different sensing designs based on nanomaterials. Finally, a summary of the current limitations and future challenges in glucose analysis is described, which may facilitate further development and applications.

Effect of dibutyl phthalate on microalgal growth kinetics, nutrients removal, and stress enzyme activities.

The dibutyl phthalate (DPB) is an emerging plasticizer contaminant that disrupts the biological processes of primary producers, especially phytoplankton. In this study, two microalgal species (Chlorella sp. GEEL-08 and Tetradesmus dimorphus GEEL-04) were exposed to various concentrations of DBP extending from 0 to 100 mg/L. The growth kinetics, N-nitrate, and P-phosphate removal efficiency were assessed. The response enzymes such as malonaldehyde (MDA) and superoxide dismutase (SOD) were also investigated. The results revealed that the Chlorella sp. GEEL-08 at 10 mg/L concentration of DBP exhibited higher growth (0.88 OD680nm) compared to T. dimorphus GEEL-04 (0.80 OD680nm). More than 94% of N and P were removed from culture media by both microalgal species. The DBP (>50 mg/L) significantly exacerbates the growth of both microalgae species and the growth inhibition ratio was in the range of 3.6%-25.9%. The SOD activity and MDA were higher in T. dimorphus culture media than in the culture media of Chlorella sp. The results reflect the hazard and the risk of plasticizers on primary producers in the ecosystem.

MOF-based sensor platforms for rapid detection of pesticides to maintain food quality and safety.

Pesticides are primarily used in agriculture to increase crop yield because of their highly lucrative, stable structure and agricultural benefits such as eliminating fungi, plant diseases, pests and insects to regulate the growth of crops. Apart from their rebel design and agricultural benefits, pesticides have severe toxicity to a variety of other living organisms. Therefore, developing effective pesticide detection systems is an ongoing challenge. Multiple technologies that for the rapid, easy, sensitive, and selective detection of these neurotoxic compounds are in demand. This paper reviews the recent advances in sensing assays based on the metal-organic framework (MOF) structure for pesticide detection. We have reviewed state-of-the-art optical biosensors for in-place sensing that have the advantages of a simple protocol, simple manipulation, super sensitivity, wide linear range, and cost-effectiveness. These biosensors use chemiluminescence with a short sensing time and a highly sensitive luminescence sensor that enables real-time detection by easy smartphone pairing. For profitable platforms, the obstacles related to sample preparation and equipment cost can be overcome by employing electrochemical sensors. The intensity, impedance, and potential difference measurement techniques used in these biosensors allow for low detection limits and observable durations in water, agricultural, and food samples containing high levels of pesticides.

State-of-the-art progress of metal-organic framework-based electrochemical and optical sensing platforms for determination of bisphenol A as an endocrine disruptor.

Considering the low concentration levels of bisphenol compounds present in environmental, food, and biological samples, and the difficulty in analyzing the matrices, the main challenge is with the cleanup and extraction process, as well as developing highly sensitive determination methods. Recent advances in the field of metal-organic frameworks (MOFs) due to their large surface area, low weight, and other extraordinary physical, chemical, and mechanical features have made these porous materials a crucial agent in developing biosensing assays. This review focuses on MOFs across their definition, structural features, various types, synthetic routes, and their significant utilization in sensing assays for bisphenol A (BPA) determination. Additionally, recent improvements in characteristics and physio-chemical features of MOFs and their functional applications in developing electrochemical and optical sensing assays via different recognition elements for detecting BPA are comprehensively discussed. Finally, the existing boundaries of the current advances including future challenges concerning successful construction of sensing approaches by employing functionalized MOFs are addressed.

Synthesis of flower-like MoS2/CNTs nanocomposite as an efficient catalyst for the sonocatalytic degradation of hydroxychloroquine.

Contamination of water resources by pharmaceutical residues, especially during the time of pandemics, has become a serious problem worldwide and concerns have been raised about the efficient elimination of these compounds from aquatic environments. This study has focused on the development and evaluation of the sonocatalytic activity of a flower-like MoS2/CNTs nanocomposite for the targeted degradation of hydroxychloroquine (HCQ). This nanocomposite was prepared using a facile hydrothermal route and characterized with various analytical methods, including X-ray diffraction and electron microscopy, which results confirmed the successful synthesis of the nanocomposite. Moreover, the results of the Brunauer-Emmett-Teller and diffuse reflectance spectroscopy analyses showed an increase in the specific surface area and a decrease in the band gap energy of the nanocomposite when compared with those of MoS2. Nanocomposites with different component mass ratios were then synthesized, and MoS2/CNTs (10:1) was identified to have the best sonocatalytic activity. The results indicated that 70% of HCQ with the initial concentration of 20 mg/L could be degraded using 0.1 g/L of MoS2/CNTs (10:1) nanocomposite within 120 min of sonocatalysis at the pH of 8.7 (natural pH of the HCQ solution). The dominant reactive species in the sonocatalytic degradation process were identified using various scavengers and the intermediates generated during the process were detected using GC-MS analysis, enabling the development of a likely degradation scheme. In addition, the results of consecutive sonocatalytic cycles confirmed the stability and reusability of this nanocomposite for sonocatalytic applications. Thus, our data introduce MoS2/CNTs nanocomposite as a proficient sonocatalyst for the treatment of pharmaceutical contaminants.

Electrochemical layered double hydroxide (LDH)-based biosensors for pesticides detection in food and environment samples: A review of status and prospects.

The need for food and agricultural resources is constantly rising, resulting in pesticide poisoning and environmental hazards. Diverse technologies collaborate to develop effective biosensors for detecting different pesticides, as it is difficult to achieve an efficient mechanism to detect pesticides. Novel solutions to reduce the cost and time for preparing samples in pesticide detection are being developed using new technologies. Moreover, methods like electrochemical techniques and fluorescence spectroscopy are now being improved to increase the sensitivity and make the operation more convenient. This article reviews the remarkable evolution in the structure of various Layered Double Hydroxides (LDHs), their various synthesis techniques, and their uses in various fields, especially in biological applications to detect pesticides in diverse contaminated samples. LDHs are layered materials with special characteristics favorable for pesticide detection. LDHs, have recently aroused increasing interest in research. We also discuss the latest advances made in the emergent strategies for improving the antimicrobial activity of LDHs.