High performance electrochemical CO2 reduction over Pd decorated cobalt containing nitrogen doped carbon.

Efficient electrocatalytic CO2 reduction reaction (eCO2RR) to various products, such as carbon monoxide (CO), is crucial for mitigating greenhouse gas emissions and enabling renewable energy storage. In this article, we introduce Pd nanoparticles which are deposited over in-house synthesized nitrogen doped tubular carbon (NC) whose ends are blocked with cobalt oxide (CoOx). This composite material is denoted as Pd@CoOx/NC. Among the series of synthesized electrocatalysts, the optimum ratio (Pd@CoOx/NC1) within this category exhibits exceptional performance, manifesting an 81% faradaic efficiency (FE) for CO generation which was quantitatively measured using a gas chromatograph. This remarkable efficiency can be attributed to several scientific factors. Firstly, the presence of Pd nanoparticles provides active sites for CO2 reduction. Secondly, the NC offer enhanced electrical conductivity and facilitate charge transfer during the reaction. Thirdly, the CoOx capping at the ends of the NC serves to stabilize the catalyst, favoring the formation of CO. The remarkable selectivity of the catalyst is further confirmed by the qualitative CO detection method using PdCl2 strips. Pd@CoOx/NC1 exhibits a high current density of 55 mA cm-2 and a low overpotential of 251 mV, outperforming Pd decorated multiwalled carbon nanotubes (Pd@MWCNTs) which shows a higher overpotential of 481 mV. Pd@CoOx/NC1 shows long-term stability at different potentials and rapid reaction kinetics. These findings highlight Pd@CoOx/NC1 as promising CO2 reduction catalysts, with implications for sustainable energy conversion techniques.

Comparative analysis of the equilibrium, kinetics, and characterization of the mechanism of rapid adsorption of Congo red on nano-biosorbents based on agricultural waste in industrial effluents.

This study aims to remove Congo red dye from industrial effluent using economical agriculturally-based nano-biosorbents like magnetic orange peel, peanut shells, and tea waste. The nano-biosorbents were characterized by various analytical techniques like SEM, FT-IR, BET and XRD. The highest adsorption capacity was obtained under the following ideal conditions: pH = 6 (orange peel and peanut shells), pH = 3 (tea waste), and dosages of nano-biosorbents with varying timeframes of 50 min for tea waste and peanut shells and 30 min for orange peel. The study found that tea waste had the highest removal rate of 94% due to its high porosity and responsible functional groups, followed by peanut shells at 83% and orange peel at 68%. The Langmuir isotherm model was found to be the most suitable, with R2 values of 0.99 for tea waste, 0.92 for orange peel, and 0.71 for peanut shells. On the other hand, a pseudo-second-order kinetic model was very feasible, showing an R2 value of 0.99 for tea waste, 0.98 for peanut shells and 0.97 for orange peel. The significance of the current study lies in its practical application, enabling efficient waste management and water purification, thereby preserving a clean and safe environment.

Recent trends in wastewater treatment by using metal-organic frameworks (MOFs) and their composites: A critical view-point.

Respecting the basic need of clean and safe water on earth for every individual, it is necessary to take auspicious steps for waste-water treatment. Recently, metal-organic frameworks (MOFs) are considered as promising material because of their intrinsic features including the porosity and high surface area. Further, structural tunability of MOFs by following the principles of reticular chemistry, the MOFs can be functionalized for the high adsorption performance as well as adsorptive removal of target materials. However, there are still some major concerns associated with MOFs limiting their commercialization as promising adsorbents for waste-water treatment. The cost, toxicity and regenerability are the major issues to be addressed for MOFs to get insightful results. In this article, we have concise the current strategies to enhance the adsorption capacity of MOFs during the water-treatment for the removal of toxic dyes, pharmaceuticals, and heavy metals. Further, we have also discussed the role of metallic nodes, linkers and associated functional groups for effective removal of toxic water pollutants. In addition to conformist overview, we have critically analyzed the MOFs as adsorbents in terms of toxicity, cost and regenerability. These factors are utmost important to address before commercialization of MOFs as adsorbents for water-treatment. Finally, some future perspectives are discussed to give directions for potential research.

Linker Engineering of Sandwich-Structured Metal-Organic Framework Composites for Optimized Photocatalytic H2 Production.

While the microenvironment around catalytic sites is recognized to be crucial in thermocatalysis, its roles in photocatalysis remain subtle. In this work, a series of sandwich-structured metal-organic framework (MOF) composites, UiO-66-NH2 @Pt@UiO-66-X (X means functional groups), is rationally constructed for visible-light photocatalytic H2 production. By varying the ─X groups of the UiO-66-X shell, the microenvironment of the Pt sites and photosensitive UiO-66-NH2 core can be simultaneously modulated. Significantly, the MOF composites with identical light absorption and Pt loading present distinctly different photocatalytic H2 production rates, following the ─X group sequence of ─H > â”€Br > â”€NA (naphthalene) > â”€OCH3  > â”€Cl > â”€NO2 . UiO-66-NH2 @Pt@UiO-66-H demonstrates H2 production rate up to 2708.2 µmol g-1  h-1 , ≈222 times that of UiO-66-NH2 @Pt@UiO-66-NO2 . Mechanism investigations suggest that the variation of the ─X group can balance the charge separation of the UiO-66-NH2 core and the proton reduction ability of Pt, leading to an optimal activity of UiO-66-NH2 @Pt@UiO-66-H at the equilibrium point.

Flow injection assays for NADH and ethanol using photosensitized rose bengal and luminol-copper (II) chemiluminescence system.

The online photoreaction of the rose bengal photosensitized luminol-copper (II) chemiluminescence (CL) system was used for the determination of ß-nicotinamide adenine dinucleotide (NADH) and ethanol (EtOH) in pharmaceutical formulations combined with a flow injection technique. NADH can significantly enhance the CL emission of the reaction. For EtOH, alcohol dehydrogenase in soluble form was utilized in the presence of nicotinamide adenine dinucleotide resulting in NADH production. The limit of detection (3σ blank, 𝑛 = 3) of 4.0 × 10-8 and 2.17 × 10-5  M, and linear range 1.3 × 10-7 to 2.5 × 10-5  M (R2  = 0.9998, n = 6) and 0.11-2.17 × 10-3  M (R2  = 0.9996, n = 6) were obtained for NADH and EtOH respectively. The injection rate was 100 h-1 with a relative standard deviation (n = 3) of 1.5-4.8% in the range studied for both analytes. The procedure was satisfactorily applied to pharmaceutical formulations with recoveries in the range 91.6 ± 3.0% to 110 ± 2.0% for NADH and 88 ± 3.0% to 95.4 ± 4.0% for EtOH. The results obtained were very consistent and did not differ considerably from the reported approaches at a 95% confidence limit. The possible mechanism of the CL reaction is also explained briefly.

Perovskite LaNiO3/Ag3PO4 heterojunction photocatalyst for the degradation of dyes.

Pristine lanthanum nickelate (LaNiO3), silver phosphate (Ag3PO4) and perovskite lanthanum nickelate silver phosphate composites (LaNiO3/Ag3PO4) were prepared using the facile hydrothermal method. Three composites were synthesized by varying the percentage of LaNiO3 in Ag3PO4. The physical properties of as-prepared samples were studied by powder X-ray diffraction (pXRD), Fourier-transform infrared (FT-IR), Scanning electron microscopy (SEM) and Energy-dispersive X-ray (EDX). Among all synthesized photocatalysts, 5%LaNiO3/Ag3PO4 composite has been proved to be an excellent visible light photocatalyst for the degradation of dyes i.e., rhodamine B (RhB) and methyl orange (MO). The photocatalytic activity and stability of Ag3PO4 were also enhanced by introducing LaNiO3 in Ag3PO4 heterojunction formation. Complete photodegradation of 50 mg/L of RhB and MO solutions using 25 mg of 5%LaNiO3/Ag3PO4 photocatalyst was observed in just 20 min. Photodegradation of RhB and MO using 5%LaNiO3/Ag3PO4 catalyst follows first-order kinetics with rate constants of 0.213 and 0.1804 min-1, respectively. Perovskite LaNiO3/Ag3PO4 photocatalyst showed the highest stability up to five cycles. The photodegradation mechanism suggests that the holes ( h +) and superoxide anion radicals O 2 • - plays a main role in the dye degradation of RhB and MO.

Three-dimensional Ni4O4-cubane metal-organic framework as a high-performance electrocatalyst for urea oxidation.

The urea oxidation reaction (UOR) is considered to be a replacement of the sluggish anodic oxygen evolution reaction (OER) in overall water-splitting. A three-dimensional (3D) nickel-containing metal-organic framework {[NiII 2(pdaa)(OH)2(H2O)] n (MOF 1) (where, H2pdaa = 1,4-phenylene diacetic acid) was investigated as a robust and highly efficient electrocatalyst for the UOR. MOF 1 comprised 1D nickel(ii) chains crosslinked through Ni4O4 cubane units to form a 3D extended network. Dangling Ni⋯OH- groups were exposed in the MOF 1 structure, and could act as active catalytic centers for the UOR. MOF 1 required a very small onset potential of 1.18 V for urea oxidation in KOH (1 M) and urea (0.33 M) and had a low Tafel slope of 38.8 mV dec-1 (in contrast to 1.84 V for the oxygen evolution reaction). The overpotential required to attain a catalytic current density of 10 mA cm-2 was 1.24 V, which is much lower than that for many materials. Controlled potential electrolysis, powder X-ray diffraction, and X-ray photoelectron spectroscopy affirmed the physicochemical integrity of the catalyst over a 17 h test reaction. This work not only addresses the problem of urea contamination, it also helps to utilize it in an energy-conversion process.

Recent progress in use of MXene in perovskite solar cells: for interfacial modification, work-function tuning and additive engineering.

The use of perovskites in photovoltaic and related industries has achieved tremendous success over the last decade. However, there are still obstacles to overcome in terms of boosting their performance and resolving stability issues for future commercialization. The introduction of a new 2D material of halide perovskites is now the key advancement in boosting the solar energy conversion efficiency. The implication of a new 2D material (MXene) in perovskite solar cells has been initiated since its first report in 2018, showing excellent transparency, electrical conductivity, carrier mobility, superior mechanical strength, and tunable work function. Based on distinctive features at the hetero-interface, halide perovskite and MXene heterostructures (HPs/Mx) have recently exhibited exceptional improvements in both the performance and stability of perovskite solar cells. Furthermore, the wide families of HPs and MXene materials allow playing with the composition and functionalities of HP/Mx interfaces by applying rational designing and alterations. In this review a comprehensive study of implementing MXenes in perovskite solar cells is presented. First, the implementation of MXenes in perovskites as an additive, and then in charge extraction layers (HTL/ETL), is described in detail. It is worth noting that still only Ti3C2Tx, Nb2CTx,V2CTx MXene is being incorporated into perovskite photovoltaics. Finally, the present obstacles in the use of MXenes in PSCS are discussed, along with the future research potential. This review is expected to provide a complete and in-depth description of the current state of research and to open up new opportunities for the study of other MXenes in PSCs.

Silane-Grafted MXene (Ti3C2T X ) Membranes for Enhanced Water Purification Performance.

The current communication describes the modifications of MXene (Ti3C2T x ) with silane grafting reaction for membrane preparation for enhanced water purification. The MXene was successfully grafted with n-octadecyltrichlorosilane (MODCS), n-octyltrichlorosilane (MNOCS), and triphenylchlorosilane (MTPCS) in order to make a hydrophobic MXene that could be able to bind with the organic matrix/polymers. The modified MXenes were transformed into thin membranes by forming an MXene/polyvinyl alcohol (PVA) composite over a filter paper support, that is, MCE (mixed cellulose ester filter paper). MXene membranes were also formed without the MCE support by using PVA and glutaraldehyde (PVA/GA) where GA was used as a cross-linker to stabilize PVA and make it water-resistant. The conditions of membrane formation were optimized to investigate optimum compatible conditions with the modified materials. The resulting membranes were tested for the removal of various organic pollutants that included mesitylene (or trimethylbenzene); polyaromatic hydrocarbons (chrysene, as a model); biphenyl; bisphenol A; benzene, toluene, ethylbenzene, and styrene; methylene blue; and Sudan II dyes. The MTPCS PVA/GA cross-linked membrane showed the best results for a pollutant removal efficiency up to 98%. Overall, all six types of membranes showed the removal efficiency in the range of 52-98%. It was observed that the membrane exhibits reusability up to five cycles.

Linker engineering in metal-organic frameworks for dark photocatalysis.

Dark reactions featuring continuous activity under light off conditions play a critical role in natural photosynthesis. However, most artificial photocatalysts are inactive upon the removal of the light source, and the artificial photocatalysts with dark photocatalysis abilities have been rarely explored. Herein, we report a Ti-based metal-organic framework (MOF), MIL-125, exhibiting the capability of dark photocatalytic hydrogen production. Remarkably, the introduction of different functional groups onto the linkers enables distinctly different activities of the resulting MOFs (MIL-125-X, X = NH2, NO2, Br). Dynamic and thermodynamic investigations indicate that the production and lifetime of the Ti3+ intermediate are the key factors, due to the electron-donating/-withdrawing effect of the functional groups. As far as we know, this is the first report on dark photocatalysis over MOFs, providing new insights into the storage of irradiation energy and demonstrating their great potential in dark photocatalysis due to the great MOF diversity.

Synthesis, characterization and application of organoclays for adsorptive desulfurization of fuel oil.

The present study encompasses the application of cost effective, organo-modified bentonite material for efficient desulfurization of model oil and real fuel. For the adsorptive desulfurization of oil, dibenzothiophene (DBT) was used as model compound. Various experimental parameters (time, temperature, adsorbent-amount and DBT concentration) were thoroughly investigated. The synthesized material was characterized via X-ray diffraction (XRD), X-ray Fluorescence (XRF), Scanning electron microscopy (SEM), Energy dispersive x-ray (EDX), Thermogravimetric analysis (TGA) and Fourier transform infrared spectroscopy (FT-IR). The modification exhibits the increase in interlayer spacing of clay as confirmed from XRD and modified material shows interesting morphology as compared to unmodified bentonite. The results showed that > 90% of DBT removal was achieved under optimized conditions for B-BTC, B-BTB and B-DSS and > 80% for B-BEHA, for model fuel oil which are greater than unmodified clay (< 45%). Additionally, the findings from desulfurization of real fuel oil declare that 96.76% and 95.83% removal efficiency was achieved for kerosene and diesel oil respectively, at optimized conditions and fuel properties follow ASTM specifications. The obtained findings well fitted with thermodynamic, isothermal (Langmuir) with adsorption capacity (70.8 (B-BTC), 66 (B-BTB), 61.2 (B-DSS) and 55.2 (B-BEHA) in mg/g) and pseudo-second-order kinetics. In thermodynamic studies, negative sign ([Formula: see text] specifies the spontaneity whereas, [Formula: see text] endothermic and positive sign [Formula: see text] show randomness after DBT adsorption onto organoclay.

Facile Synthesis of a Novel Ni-WO3@g-C3N4 Nanocomposite for Efficient Oxidative Desulfurization of Both Model and Real Fuel.

The current study comprises the successful synthesis of a Ni-WO3@g-C3N4 composite as an efficient and recoverable nanocatalyst for oxidative desulfurization of both model and real fuel oils. The physiochemical characterization of the synthesized composite was confirmed via Fourier transform infrared spectroscopy, X-ray diffraction, scanning electron microscopy (SEM), energy-dispersive X-ray spectroscopy, and thermogravimetric analysis. SEM results showed that Ni-WO3 particles were well-decorated on the g-C3N4 surface with an interesting morphology as appeared on the surface like spherical particles. The obtained findings revealed that 97% dibenzothiophene (DBT) removal can be achieved under optimized conditions (0.1 g of the catalyst, 1 mL of an oxidant, 100 mg/L DBT-based model fuel, a time duration of 180 min, and a temperature of 40 °C). Additionally, the catalytic activity for real fuel was also investigated in which 89.5 and 91.2% removal efficiencies were achieved for diesel and kerosene, respectively, as well as fuel properties following ASTM specifications. A pseudo first-order kinetic model was followed well for this reaction system, and the negative value of ΔG was due to the spontaneous process. Additionally, the desulfurization study was optimized via a response surface methodology (RSM/Box-Behnken design) for predicting optimum removal of sulfur species by drawing three-dimensional RSM surface plots. The Ni-WO3@g-C3N4 proved to be a promising catalyst for desulfurization of fuel oil by exhibiting reusability of five times with no momentous decrease in efficiency.

Exploration of microplastic pollution with particular focus on source identification and spatial patterns in riverine water, sediment and fish of the Swat River, Pakistan.

Microplastics (MPs) have been reported as an emerging xenobiotic organic pollutant in freshwater ecosystems and a universal hazard for ecosystems because of the rapid increase in global demand. The present study was conducted to explore MPs' occurrence, abundance and spatial distribution in sediment, water and Schizothorax plagiostomus samples, collected from the Swat River. ATR-FTIR spectroscopy was used for chemical characterization of visually identified MPs by using standard protocols such as digestion using H2O2, density separation using ZnCl2, vacuum filtration with borosilicate glass micro filter papers and digital microscopy using a stereomicroscope connected with a camera. Range of mass abundance of identified MPs in river sediments, river water, tributaries sediment and tributary water was found to be 0.6-2.5 mg kg-1, 0.7-3.8 mg L-1, 0.9-4.5 mg kg-1 and 0.6-1.1 mg L-1 respectively. Meanwhile, in Schizothorax plagiostomus digestive tracts samples, it was 0.6-1.9 mg per fish. Numeric abundance of MPs in all matrices was found to be tributary sediment (202 items per kg) > river water (192 items per L) > river sediment (182 items per kg) > fish (153 items per fish) > tributary water (92 items per L). MPs identified on the basis of morphology in all matrices were found to be fragments > fibers > pellets > films > foams. MPs were dominant in all urban stations while their spatial distribution along with the study site was heterogeneous due to the surroundings such as tourist spots, hydrodynamic conditions, and proximity to urban areas, plastic industries and due to recharge by the highly contaminated tributaries. The MPs identified on the basis of size dimensions show that S1 (0.5-1 mm) in all matrices was highest while S2 (1-5 mm) was the lowest. Primary source MPs identified were fibers, films, fragments and foams particles while secondary sources were pellets. Results of ATR-FTIR showed that PE was the most common plastic type identified in all samples followed by PVC, PET, PP and PS. This is the first study exploring the MPs' occurrence, numeric and mass abundance and spatial distribution in the SR ecosystem. The present study may be a valuable reference for better understanding the MPs' pollution in Pakistan. The findings of the present study can help to identify the potential sources (i.e., primary and secondary) of MPs to improve waste management in the Swat District and model the transport fluxes of these microplastics in other rivers using water quality parameters and basin characteristics.

Coumarin based thiosemicarbazones as effective chemosensors for fluoride ion detection.

Anion sensing have attained immense importance as these charged ions are prevailing in agriculture industry and in heavy industry and therefore in the environment around us, chemosensors are commencing to claim several applications as their role is being better perceived day by day. In the current study, coumarin based thiosemicarbazone R-1 (phenyl moiety) and R-2 (benzyl moiety) were synthesized. It was observed that there were variations in the sensing patterns of compound bearing benzyl group, as compared to the simple phenyl group bearing receptor. Different techniques were used to confirm the interaction of coumarin based receptors with anions. These techniques included naked-eye test, UV-visible, 1H NMR, and fluorescence spectroscopic techniques. The synthesized receptors showed selectivity for fluoride ions. Benesi-Hildebrand equation was employed for determining the detection limits and binding constants values. The synthesized receptors were employed as efficient chemosensors in real life samples and satisfactory results were obtained.

Occurrence, influencing factors, toxicity, regulations, and abatement approaches for disinfection by-products in chlorinated drinking water: A comprehensive review.

Disinfection is considered as a vital step to ensure the supply of clean and safe drinking water. Various approaches are adopted for this purpose; however, chlorination is highly preferred all over the world. This method is opted owing to its several advantages. However, it leads to the formation of certain by-products. These chlorination disinfection by-products (DBPs) are genotoxic, carcinogenic and mutagenic. Still chlorination is being practiced worldwide. Present review gives insights into the occurrence, toxicity and factors affecting the formation of regulated (THMs, HAAs) and emerging DBPs (N-DBPs, HKs, HAs and aromatic DBPs) found in drinking water. Furthermore, remediation techniques used to control DBPs have also been summarized here. Key findings are: (i) concentration of regulated DBPs surpassed the permissible limit in most of the regions, (ii) high chlorine dose, high NOM, more reaction time (up to 3 h) and high temperature (up to 30 °C) enhance the formation of THMs and HAAs, (iii) high pH favors the formation of THMs while low pH is suitable of the formation of HAAs, (iv) high NOM, low temperature, low chlorine dose and moderate pH favors the formation of unstable DBPs (N-DBPs, HKs and HAs), (v) DBPs are toxic not only for humans but for aquatic fauna as well, (vi) membrane technologies, enhanced coagulation and AOPs remove NOM, (vii) adsorption, air stripping and other physical and chemical methods are post-formation approaches (viii) step-wise chlorination is assumed to be an efficient method to reduce DBPs formation without any treatment. Toxicity data revealed that N-DBPs are found to be more toxic than C-DBPs and aromatic DBPs than aliphatic DBPs. In majority of the studies, merely THMs and HAAs have been studied and USEPA has regulated just these two groups. Future studies should focus on emerging DBPs and provide information regarding their regulation.

A practical approach for synthesis of biodiesel via non-edible seeds oils using trimetallic based montmorillonite nano-catalyst.

The potential of new trimetallic (Ce, Cu, La) loaded montmorillonite clay catalyst for synthesizing biodiesel using novel non-edible Celastrus paniculatus Willd seed oil via two-step transesterification reaction has been reported along with catalyst characterization. Transesterification reaction was optimized and maximum biodiesel yield of 89.42% achieved under optimal operating reaction states like; 1:12 oil to methanol ratio, 3.5% of catalyst amount, 120 °C of reaction temperature for 3 h. The predicted and experimental biodiesel yields under these reaction conditions were 89.42 and 89.40%, which showing less than 0.05% variation. Additionally, optimum biodiesel yield can be predicted by drawing 3D surface plots and 2D contour plots using MINITAB 17 software. For the characterization of the obtained biodiesel, analysis including the GC/MS, FT-IR, 1H NMR and 13C NMR were applied. The fuel properties of obtained biodiesel agrees well with the different European Union (EU-14214), China (GB/T 20828), and American (ASTM-951, 6751) standards.

Novel surfactant stabilized PLGA cisplatin nanoparticles for drug delivery applications.

In the current study, cisplatin loaded (Poly(lactic-co-glycolicacid)) (PLGA) stabilized with 4-phenylphenacylbromide based surfactants nanoparticles were developed for drug delivery applications. For the course of this study four new 4-phenylphenacylbromide based compounds abbreviated as PA(C2)3, PA(C8)3, PAC16 and PAC18 have been synthesized by the reaction of 4-phenylphenacylbromide with various long chain amines. The new surfactants were characterized with 1H and 13C NMR and FTIR spectroscopy. The critical micelle concentration (CMC) of newly synthesized surfactants are in the range of 0.024-0.091 mM. The newly synthesized surfactants have been incorporated in PLGA based nanoparticles and are used for drug encapsulation and delivery of cisplatin. The drug encapsulation efficiency for newly fabricated nanoparticles was found to be in the range of 65 ± 1.5 to 67 ± 1.6%, the drug loading was observed in the range of 1.96 ± 0.11 to 2.31 ± 0.19%, whereas the maximum drug release was found to be 85.1 ± 1.1%.

Dechlorane Plus as an emerging environmental pollutant in Asia: a review.

Dechlorane Plus (DP) is an unregulated, highly chlorinated flame retardant. It has been manufactured from past 40 years but its presence in the environment was initially reported in 2006. Later, it has been found in various biotic and abiotic environmental matrices. However, little attention has been paid to monitor its presence in Asia. Many studies have reported the occurrence of DP in the environment of Asia, yet the data are scarce, and studies are limited to few regions. The objective of present review is to summarize the occurrence, distribution, and toxicity of this ubiquitous pollutant in various environmental matrices (biotic and abiotic). DP has also been reported in the areas with no emission sources, which proves its long-range transport. Moreover, urbanization and industrialization also affect the distribution of DP, i.e., high levels of DP have been found in urban areas relative to the rural. Tidal movement also incorporates in transport of DP across the aquatic system. Further, bioaccumulation trend of DP in various tissues is kidney > liver > muscle tissues, whereas, blood brain barrier resists its accumulation in brain tissues. Additionally, gender-based accumulation trends revealed high DP levels in females in comparison to males due to strong metabolism of males. Furthermore, methodological aspects and instrumental analysis used in previous studies have also been summarized here. However, data on biomagnification in aquatic ecosystem and bioaccumulation of DP in terrestrial food web are still scarce. Toxicity behavior of syn-DP and anti-DP is still unknown which might gain the interest for future studies.

Comparative efficacy of mitigation techniques for the detoxification of Prunus persica (L.) from selected pesticide residues.

Fruits are the valuable and important components of human diet. Among them, Prunus persica is a rich source of different minerals and dietary fibers. In Pakistan, the total annual production of P. persica is approximately 837,000 tons. In order to enhance agricultural yield and quality, the plant protection agents are employed during fruit production. Ultimately, this in turn leads to the incorporation of pesticide residues in fruits. In present study, an effort has been made for the determination of three selected pesticide residues, i.e., chlorpyrifos (CPF), difenoconazole (DFN), and carbendazim (CRB) in samples of P. persica collected from Swat territory. Samples were analyzed through high performance liquid chromatography (HPLC). Results revealed the occurrence of all three pesticides in studied samples; however, levels of CPF and DFN were found to be higher than MRLs. Moreover, the effects of different mitigation techniques revealed that highest reduction of CPF, DFN, and CRB (86%, 97%, 89%) residues was obtained by treatment with 10% CH3COOH followed by 10% NaCl (74%, 78%, 84%). The lowest reduction was obtained by treatment with 10% solution of NaOH (52%, 55%, 63%).

Environmental risk assessment of diclofenac residues in surface waters and wastewater: a hidden global threat to aquatic ecosystem.

Pharmaceuticals are chemical compounds employed as medicinal drugs. They have severe physic-chemical properties which make them destructive for non-target species. Consequently, their continuous addition in the environment may pose hazardous effects. Among these, diclofenac (DCF), a non-steroidal anti-inflammatory drug (NSAID), is extensively used in Pakistan which may lead to its accumulation in both terrestrial and aquatic environment. Present study aims to assess the presence and concentration of pharmaceutically active drug (DCF) in surface water and wastewater of twin cities of Pakistan (Rawalpindi and Islamabad). For this purpose, a validated high-performance liquid chromatography (HPLC) method was adopted involving solid-phase extraction procedure. Wastewater samples were collected from various sites of Rawalpindi and Islamabad. Results of HPLC analysis revealed that DCF was extant with considerably high concentration, not only in wastewater but also in surface water samples. Concentrations as high as 216 µg L-1 was detected in Rawat industrial area and low as 8 µg L-1 was detected in dairy farm wastewater samples collected from Taramri. However, maximum DCF levels in residential wastewater and hospital wastewater were detected to be 105 µg L-1 and 34 µg L-1, respectively. Moreover, the highest detected level (116 µg L-1) was found in surface water of Sawan River. Further, results of ecological risk assessment revealed its possible toxic effects of DCF on various aquatic organisms.