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In this research work, surface-modified nano zerovalent copper (nZVC) was prepared using a simple borohydride reduction method. The spectroscopic and crystallographic results revealed the successful synthesis of surface-modified nano zerovalent copper (nZVC) using solvents such as ethanol (ETOH), ethylene glycol (EG) and tween80 (T80). The as-synthesized material was fully characterized for morphological surface and crystal structural properties. The results indicated that EG provides an excellent synthesis environment to nZVC compared to ETOH and T80 in terms of good dispersion, high surface area and excellent catalytic properties. The catalytic efficiency of nZVC/EG was investigated alone and with peroxymonosulphate (PMS) in the absence of light. The degradation results demonstrated that the involvement of PMS synergistically boosted the catalytic efficiency of synthesized nZVC/EG material. Furthermore, the degradation products (DPs) of CBZ were determined by GC-MS and subsequently, the degradation pathways were proposed. The ecotoxicity analysis of the DPs was also explored. The proposed (nZVC/EG/PMS) system is economical and efficient and thus could be applied for the degradation of CBZ from an aquatic system after altering the degradation pathways in such a way that results in harmless products.

Batch scale removal of arsenic (As) from aqueous media was explored using nano-zero valent iron (Fe 0 ) and copper (Cu 0 ) particles. The synthesized particles were characterized using a Brunauer-Emmett-Teller (BET) surface area analyzer, a scanning electron microscope (SEM), and Fourier transform infrared spectroscopy (FTIR). The BET result showed that the surface area (31.5 m 2 /g) and pore volume (0.0415 cm 3 /g) of synthesized Fe 0 were higher than the surface area (17.56 m 2 /g) and pore volume (0.0287 cm 3 /g) of Cu 0 . The SEM results showed that the morphology of the Fe 0 and Cu 0 was flowery microspheres and highly agglomerated with thin flakes. The FTIR spectra for Fe 0 showed broad and intense peaks as compared to Cu 0 . The effects of the adsorbent dose (1-4 g/L), initial concentration of As (2 mg/L to 10 mg/L) and solution pH (2-12) were evaluated on the removal of As. Results revealed that effective removal of As was obtained at pH 4 with Fe 0 (94.95%) and Cu 0 (74.86%). When the dosage increased from 1 to 4 g L -1 , the As removal increased from 70.59 to 93.02% with Fe 0 and from 67 to 70.59% with Cu 0 . However, increasing the initial As concentration decreased the As removal significantly. Health risk indices, including estimated daily intake (EDI), hazard quotient (HQ), and cancer risk (CR) were employed and a significant decline (up to 99%) in risk indices was observed in As-treated water using Fe 0 /Cu 0 . Among the adsorption isotherm models, the values of R 2 showed that isothermal As adsorption by Fe 0 and Cu 0 was well explained by the Freundlich adsorption isotherm model (R 2  > 0.98) while the kinetic experimental data was well-fitted with the Pseudo second order model. The Fe 0 showed excellent stability and reusability over five sorption cycles, and it was concluded that, compared to the Cu 0 , the Fe 0 could be a promising technology for remediating As-contaminated groundwater., (© 2023. The Author(s), under exclusive licence to Springer Nature B.V.)

Chromium (Cr), due to its greater contamination in aquifers and distinct eco-toxic impacts, is of greater environmental concern. This study aimed to synthesize nanocomposites of almond shells biochar (BC) with zerovalent bismuth and/or copper (Bi 0 /BC, Cu 0 /BC, and Bi 0 -Cu 0 /BC) for the removal of Cr from aqueous solution. The synthesized nanocomposites were investigated using various characterization techniques such as XRD, FTIR spectroscopy, SEM, and EDX. The Cr removal potential by the nanocomposites was explored under different Cr concentrations (25-100 mg/L), adsorbent doses (0.5-2.0 g/L), solution pH (2-8), and contact time (10-160 min). The above-mentioned advanced techniques verified successful formation of Bi 0 /Cu 0 and their composite with BC. The synthesized nanocomposites were highly effective in the removal of Cr. The Bi 0 -Cu 0 /BC nano-biocomposites showed higher Cr removal efficiency (92%) compared to Cu 0 /BC (85%), Bi 0 /BC (76%), and BC (67%). The prepared nanocomposites led to effective Cr removal at lower Cr concentrations (25 mg/L) and acidic pH (4.0). The Cr solubility changes with pH, resulting in different degrees of Cr removal by Bi 0 -Cu 0 /BC, with Cr(VI) being more soluble and easier to adsorb at low pH levels and Cr(III) being less soluble and more difficult to adsorb at high pH levels. The experimental Cr adsorption well fitted with the Freundlich adsorption isotherm model (R 2  > 0.99) and pseudo-second-order kinetic model. Among the prepared nanocomposites, the Bi 0 -Cu 0 /BC showed greater stability and reusability. It was established that the as-synthesized Bi 0 -Cu 0 /BC nano-biocomposite showed excellent adsorption potential for practical Cr removal from contaminated water., (© 2023. The Author(s), under exclusive licence to Springer Nature B.V.)

Organochlorine pesticides (OCPs) have been used extensively as insecticides and herbicides. This study investigates the occurrence of lindane in surface water from the Peshawar valley ( i.e. , Peshawar, Charsadda, Nowshera, Mardan and Swabi districts of Khyber Pakhtunkhwa, Pakistan). Out of 75 samples tested ( i.e. , 15 samples from each district), 13 samples (including 2 from Peshawar, 3 from Charsadda, 4 from Nowshera, 1 from Mardan, and 3 from Swabi) are found to be contaminated with lindane. Overall, the detection frequency is 17.3%. The maximum concentration of lindane is detected in a water sample from Nowshera and found to be 2.60 μg L -1 . Furthermore, the degradation of lindane in the water sample from Nowshera, containing the maximum concentration, is investigated by simulated solar-light/TiO 2 (solar/TiO 2 ), solar/H 2 O 2 /TiO 2 and solar/persulfate/TiO 2 photocatalysis. The degradation of lindane by solar/TiO 2 photocatalysis is 25.77% after 10 h of irradiation. The efficiency of the solar/TiO 2 process is significantly increased in the presence of 500 μM H 2 O 2 and 500 μM persulfate (PS) (separately), represented by 93.85 and 100.00% lindane removal, respectively. The degradation efficiency of lindane is lower in natural water samples as compared to Milli-Q water, attributed to water matrix effect. Moreover, the identification of degradation products (DPs) shows that lindane follows similar degradation pathways in natural water samples as the one in Milli-Q water. The results show that the occurrence of lindane in surface waters of Peshawar valley is a matter of great concern for human beings and the environment. Interestingly, H 2 O 2 and PS assisted solar/TiO 2 photocatalysis is an effective method for the removal of lindane from natural water., Competing Interests: There are no conflicts of interest to declare., (This journal is © The Royal Society of Chemistry.)

Binary composite of zerovalent iron and titanium dioxide (Fe 0 /TiO 2 ) was synthesized for the catalytic removal of dichlorophene (DCP) in the presence of peroxymonosulfate (PMS). The as-prepared composite (Fe 0 /TiO 2 ) exhibits synergistic effect and enhanced properties like improved catalytic activity of catalyst and greater magnetic property for facile recycling of catalyst. The results showed that without addition of PMS at reaction time of 50 min, the percent degradation of DCP by TiO 2 , Fe 0 , and Fe 0 /TiO 2 was just 5%, 11%, and 12%, respectively. However, with the addition of 0.8 mM PMS, at 10 min of reaction time, the catalytic degradation performance of Fe 0 , TiO 2 , and Fe 0 /TiO 2 was significantly improved to 82%, 18%, and 88%, respectively. The as-prepared catalyst was fully characterized to evaluate its structure, chemical states, and morphology. Scanning electron microscopy results showed that in composite TiO 2 causes dispersion of agglomerated iron particles which enhances porosity and surface area of the composites and X-ray diffraction (XRD), energy dispersive X-ray (EDX), and Fourier-transform infrared (FTIR) results revealed successful incorporation of Fe 0 , and oxides of Fe and TiO 2 in the composite. The adsorption-desorption analysis verifies that the surface area of Fe 0 /TiO 2 is significantly larger than bare Fe 0 and TiO 2. Moreover, the surface area, particle size, and crystal size of Fe 0 /TiO 2 was surface area = 85 m 2  g -1 , particle size = 0.35 μm, and crystal size = 0.16 nm as compared to TiO 2 alone (surface area = 22 m 2  g -1 , particle size = 4.25 μm, and crystal size = 25.4 nm) and Fe 0 alone (surface area = 65 m 2  g -1 , particle size = 0.9 μm, and crystal size = 7.87 nm). The as-synthesized material showed excellent degradation performance in synthesized wastewater as well. The degradation products and their toxicities were evaluated and the resulted degradation mechanism was proposed accordingly. The toxicity values decreased in order of DP1 > DP5 > DP2 > DP3 > DP4 and the LC 50 values toward fish for 96-h duration decreased from 0.531 to 67.2. This suggests that the proposed technology is an excellent option for the treatment of antibiotic containing wastewater., (© 2022. The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature.)

Water is obligatory for sustaining life on Earth. About 71% of the Earth's surface is covered in water. However, only one percent of the total water is drinkable. The presence of contaminants in wastewater, surface water, groundwater, and drinking water is a serious threat to human and environmental health. Their toxic effects and resistance towards conventional water treatment methods have compelled the scientific community to search for an environmentally friendly method that could efficiently degrade toxic contaminants. In this regard, visible light active photocatalysts have proved to be efficient in eliminating a wide variety of water toxins. A plethora of research activities have been carried out and significant amounts of funds are spent on the monitoring and removal of water contaminants, but relatively little attention has been paid to the degradation of persistent water pollutants. In this regard, nanoparticles of doped ZnO are preferred options owing to their low recombination rate and excellent photocatalytic and antimicrobial activity under irradiation of solar light. The current article presents the roles of these nanomaterials for wastewater treatment from pollutants of emerging concern.

In this study, biochar was prepared from Sidr plant leaves and used for the treatment of ciprofloxacin (CIP)-contaminated water. CIP is important class of emerging water pollutants from pharmaceutical industries. The biochar showed 65% adsorption efficiency and 43.48 mg/g adsorption capacity of CIP. Adsorption efficiency as well as adsorption capacity were improved to 91% and 62.50 mg/g, respectively, by phosphoric acid (H 3 PO 4 ) modified biochar. Removal of CIP by the prepared biochar was due to different surface functional groups of CIP and biochar as revealed from the study of different characterization analyses. The presence of PO 4 group in modified biochar led to maximum binding of CIP. Also, the modified biochar showed higher reusability potential and less leaching of ions when compared to the raw biochar. Removal of CIP was affected by concentrations of CIP, the amount of biochar and different pH's; the maximum removal of CIP was achieved at pH 4. The Freundlich and 3- group in modified biochar led to maximum binding of CIP. Also, the modified biochar showed higher reusability potential and less leaching of ions when compared to the raw biochar. Removal of CIP was affected by concentrations of CIP, the amount of biochar and different pH's; the maximum removal of CIP was achieved at pH 4. The Freundlich and pseudo-first-order models best fitted the removal of CIP by modified biochar. Advanced characterization techniques were applied to investigate surface and physiological characteristics of the biochar and modified biochar. The modification showed high impact on the performance and stability of biochar. The study showed significant impacts of modification on the potential of the biochar for treatment of CIP-contaminated water.

This study reported Fe doped zinc oxide (Fe-ZnO) synthesis to degrade chlorpyrifos (CPY), a highly toxic organophosphate pesticide and important sources of agricultural wastes. Fourier transform infrared, X-ray diffraction, scanning electron microscope, and energy-dispersive X-ray spectroscopic analyses showed successful formation of the Fe-ZnO with highly crystalline and amorphous nature. Water collected from agricultural wastes were treated with Fe-ZnO and the results showed 67% degradation of CPY by Fe-ZnO versus 39% by ZnO at 140 min treatment time. Detail mechanism involving reactive oxygen species production from solar light activated Fe-ZnO and their role in degradation of CPY was assessed. Use of H 2 O 2 , peroxydisulfate (S 2 O 8 2- ) and peroxymonosulfate (HSO 5 - ) with Fe-ZnO under solar irradiation promoted removal of CPY. The peroxides yielded hydroxyl (OH) and sulfate radical () under solar irradiation mediated by Fe-ZnO. Effects of several parameters including concentration of pollutant and oxidants, pH, co-existing ions, and presence of natural organic matter on CPY degradation were studied. Among peroxides, HSO 5 - revealed to provide better performance. The prepared Fe-ZnO showed high reusability and greater mineralization of CPY. The GC-MS analysis showed degradation of CPY resulted into several transformation products (TPs). Toxicity analysis of CPY as well as its TPs was performed and the formation of non-toxic acetate imply greater capability of the treatment technology., (Copyright © 2021 Elsevier Ltd. All rights reserved.)

In this work, bismuth-doped titania (Bi x TiO 2 ) with improved oxygen vacancies was synthesized by sol-gel protocol as a novel peroxymonosulfate (PMS, HSO 5 - ) activator. HSO 5 - and adsorbed oxygen molecules could efficiently be transformed into their respective radicals through defect ionization to attain charge balance after their trapping on oxygen vacancies of the catalyst. XRD study of Bi x TiO 2 with 5 wt% Bi (5BiT) revealed anatase, crystalline nature, and successful doping of Bi into TiO 2 crystal lattice. The particle size obtained from BET data and SEM observations was in good agreement. PL spectra showed the formation rates of • OH by 3BiT, 7BiT, 5BiTC, and 5BiT as 0.720, 1.200, 1.489, and 2.153 μmol/h, respectively. 5BiT catalyst with high surface area (216.87 m 2 g -1 ) and high porosity (29.81%) was observed the excellent HSO 5 - activator. The catalytic performance of 0BiT, 3BiT, 5BiT, and 7BiT when coupled with 2 mM HSO 5 - for recalcitrant flumequine (FLU) removal under dark was 10, 27, 55, and 37%, respectively. Only 5.4% decrease in catalytic efficiency was observed at the end of seventh cyclic run. Radical scavenging studies indicate that SO 4 •- is the dominant species that caused 62.0% degradation. Moreover, strong interaction between Bi and TiO 2 through Bi-O-Ti bonds prevents Bi leaching (0.081 mg L -1 ) as shown by AAS. The kinetics, degradation pathways, ecotoxicity, and catalytic mechanism for recalcitrant FLU were also elucidated. Cost-efficient, environment-friendly, and high mineralization recommends this design strategy; Bi x TiO 2 /HSO 5 - system is a promising advanced oxidation process for the aquatic environment remediation.

Congo-red (CR), a precursor of textile products and a contaminant of great concern, has contaminated aquatic environments. Here, we explored the synthesis of mesoporous nano-zerovalent manganese (nZVMn) and Phoenix dactylifera leaves biochar (PBC) composite for the removal of CR from water. The nZVMn/PBC adsorbed 117.647 mg/g of CR versus 25.316 mg/g by PBC at [CR] 0 = 20 mg/L and [PBC] 0 = [nZVMn/PBC] 0 = 500 mg/L. Variation of [nZVMn/PBC] 0 , [CR] 0 and pH influenced the adsorption of CR. Freundlich adsorption isotherm and pseudo-first-order kinetic models best fitted CR adsorption. The H 2 O 2 coupling with nZVMn/PBC promoted removal of CR possibly due to the formation of hydroxyl radical ( ● OH) and caused 95 % removal of CR versus 77 % by nZVMn/PBC alone. The ● OH scavengers inhibited the removal of CR. The nZVMn/PBC showed a good reusability and efficient removal of CR up to the seventh cycle of treatment. Results reveal that nZVMn improved performance, thermal stability and reusability of biochar. Degradation products from ● OH-mediated degradation of CR were studied by ultraperformance liquid chromatography with mass spectrometric detector to establish degradation pathways. The ion-chromatographic analysis showed the formation of non-toxic inorganic acetate product, which suggests high potential of the newly fabricated adsorbent in the removal of CR., (Copyright © 2020 Elsevier B.V. All rights reserved.)

In this study, we showed that doping bismuth (Bi) at the surface of Fe 0 (Bi/Fe 0 , bimetallic iron system)-synthesized by a simple borohydride reduction method-can considerably accelerate the reductive degradation of chloramphenicol (CHP). At a reaction time of 12 min, 62, 68, 74, 95, and 82% degradation of CHP was achieved with Fe 0 , Bi/Fe 0 -1 [1% (w/w) of Bi], Bi/Fe 0 -3 [3% (w/w) of Bi], Bi/Fe 0 -5 [5% (w/w) of Bi], and Bi/Fe 0 -8 [8% (w/w) of Bi], respectively. Further improvements in the degradation efficiency of CHP were observed by combining the peroxymonosulfate (HSO 5 - ) with Bi/Fe 0 -5 (i.e., 81% by Bi/Fe 0 -5 and 98% by the Bi/Fe 0 -5/HSO 5 - system at 8 min of treatment). Interestingly, both Fe 0 and Bi/Fe 0 -5 showed effective H 2 production under dark conditions that reached 544 and 712 μM by Fe 0 and Bi/Fe 0 -5, respectively, in 70 mL of aqueous solution containing 0.07 g (i.e., at 1 g L -1 concentration) of the catalyst at ambient temperature., Competing Interests: The authors declare no competing financial interest., (© 2020 American Chemical Society.)

Globally, a large number of school-aged children is suffering from water-borne diseases, particularly in low-income countries. Arsenic (As) is a hazardous and potentially carcinogenic metal(loid) in drinking water. Nowadays, alarming levels of As have been reported in the groundwater of Vehari District, Punjab Pakistan. In this study, drinking water supplies for high and higher secondary schools were examined in Vehari District. A total of 164 water samples were collected from schools and subjected to heavy metal(loid) analysis (As) and basic water physicochemical parameters. The results were analyzed with respect to sampling area, school type, school education level, sources of sample collection, and the depth of the source. The results revealed that As concentration of water samples in boys' and girls' schools was 12.8 μg/L and 9.2 μg/L, respectively. However, when the As concentration in drinking water was evaluated at the school education level, a notable higher concentration of As was observed in the higher secondary schools than the high schools with an average of 19.5 and 9.7 μg/L, respectively. The risk assessment indices were calculated based on education level and different age groups of the children (primary, elementary, high, and higher secondary). High carcinogenic (cancer risk = 0.001) and non-carcinogenic (hazard quotient = 2.0) risks were noted for the children in higher secondary school. The current findings anticipated that the drinking water of schools in Vehari District did not meet the requirement of the World Health Organization (WHO) drinking water quality guidelines. Safe drinking water is crucial for the development and growth of children. Therefore, it is important for educational authorities to take steps for provision of As free safe drinking water to students and local inhabitants.

Removal of cadmium (Cd 2+ ), a highly toxic heavy metal, from aqueous solutions was investigated using nano zerovalent iron (Fe 0 ). Cadmium was efficiently removed by Fe 0 , although reactivity and reusability of Fe 0 was significantly promoted by coupling with bismuth (Bi). At a reaction time of 20 min, 85% and 96% Cd 2+ was removed by Fe 0 and Bi/Fe 0 , respectively, at first cycle using [Cd 2+ ] 0  = 10 mg/L and [Fe 0 ] 0  = [Bi/Fe 0 ] 0  = 1.0 g/L. However, Cd 2+ removal efficiency was reduced to 12% and 80% at sixth cycle by Fe 0 and Bi/Fe 0 , respectively. The X-Ray diffraction and energy dispersive X-Ray spectroscopy analysis proved successful formation of Fe 0 by the chemical reduction method and also confirmed coupling of Bi with Fe 0 to form bimetallic Bi/Fe 0 . The oxidation of Fe 0 and Bi/Fe 0 yielded electron that played significant role in the conversion of toxic Cd 2+ into non-toxic Cd 0 . The reactivity of electron with Cd 2+ was calculated to be 4.3 × 10 9  M -  s 1  s -1 . The pH of solution showed pronounced effects on the reactivity of both Fe 0 and Bi/Fe 0 . Removal of Cd 2+ by both Fe 0 and Bi/Fe 0 followed pseudo-first-order kinetic model. The conversion of Cd 2+ into non-toxic Cd 0 proved Fe 0 and Bi/Fe 0 to be highly efficient and rewarding in detoxification of Cd 2+ and other toxic metals in aqueous environments., (Copyright © 2019 Elsevier B.V. All rights reserved.)

Soil contamination with heavy metals is a global issue confronting the environmental pollution and human/animal health. Much work has been done on physiological and antioxidant responses of wheat in hydroponic experiments and health risks from individual heavy metal contamination to human, but limited information is available on their combined application in soil. Therefore, this pot study delineates the uptake of lead and cadmium, as well as physiological responses of wheat and associated health risks under different levels of alone and combined Cd and Pb treatments. Metal uptake increased with their increasing applied levels. The highest Cd (4.24, 1.38, and 0.92 mg kg -1 ) and Pb (763.33, 39.63, and 16.35 mg kg -1 ) concentrations in root, shoot, and grain, respectively, were observed at highest applied levels (0.4 mM Cd and 10 mM Pb). Furthermore, all the treatments increased lipid peroxidation and activities of superoxide dismutase, catalase, ascorbate peroxidase, and peroxidase, while decreased total chlorophyll contents and membrane stability index. Under combined application of Cd and Pb, the toxicity and detoxification responses of wheat increased compared to alone treatments. Multivariate analysis further confirmed the toxicity and accumulation pattern of metals under alone and combined treatments. Target hazard quotient values of Cd and Pb were < 1 under alone and combined treatments. The health hazard index values of Pb (97.07 and 87.89%) were higher than those of Cd (2.93 and 12.10%) in combined application for human and buffalo, respectively. This study highlights that the multi-metal contamination (Cd and Pb) is detrimental for wheat growth and human/animal health.

This paper comprises a comprehensive kinetic study for the adsorptive removal of As (V) from aqueous medium by mixed oxide (MO) of iron and silicon. The multi-linearity of the intraparticle diffusion model pointed towards the likelihood of both the pore and film diffusion. The Boyd model validated film diffusion to be the principal mechanism responsible for controlling the rate of the arsenate adsorption on MO. The negative entropy of activation (ΔS # ) suggested the adsorption mechanism to be associative in nature. The non-negative values of ΔG # suggested the presence of an energy barrier to be surmounted for the reaction to occur.

The removal of brilliant green (BG), a toxic organic and cationic dye, has been examined by UV/S 2 O 8 2- (PS), UV/HSO 5 - (PMS) and UV/H 2 O 2 processes. BG showed insignificant direct photolysis at 254 nm (i.e., 8.6% after 30 min). However, enhanced BG degradation was observed in UV/PS, UV/PMS and UV/H 2 O 2 systems as revealed from 63.1, 47.0 and 34.8% BG degradation, respectively, at 30 min of reaction time, using 0.05 mM BG and 1.0 mM oxidant initial concentration. The bimolecular rate constants of OH and SO 4 - s 9 and 2.21 × 10 9 M -1 s -1 , respectively. Electrical energy per order (EE/O) values for UV/PS, UV/PMS and UV/H 2 O 2 processes were calculated to be 5.4, 6.8, and 7.8 KWh/m 3 /order, respectively. The addition of humic acid (HA) and inorganic anions inhibited the degradation of BG by UV/PS in the order of NO 2 -  > HA > HCO 3 -  > Cl -   > NO 3 -  ≈ SO 4 2- . The results of frontier electron densities (FEDs) showed that C-atom holding the three rings (C7), and C-atoms at para positions to N-alkyl groups of the two rings (C4 and C14) are the predominant sites for radical addition. Furthermore, nine degradation products (DPs) of BG were detected experimentally using LC/MS/MS., (Copyright © 2018 Elsevier B.V. All rights reserved.)

Despite significant recent advancement in research, biogeochemical behavior of heavy metals with respect to their applied form is still topical. Moreover, metal toxicity to plants may vary with their stage of development/maturity. Therefore, this study for the first time evaluated the influence of ethylenediaminetetraacetic acid (EDTA) and citric acid (CA) on cadmium (Cd) accumulation and toxicity to germinating and young pea seedlings as well as in younger and older leaves. The experimental setup of current study consisted of two separate studies. The first study was performed on germinating seedlings grown in a Cd-contaminated sand media. Pea seeds were treated with two levels of Cd (Cd-25 and Cd-100) alone and combined with different levels of EDTA and CA. The second study was carried out in hydroponic solution. The influence of organic amendments on Cd accumulation and toxicity to pea plants was evaluated by determining Cd contents in pea seedlings, H 2 O 2 contents, chlorophyll contents and lipid peroxidation in younger and older leaves. Cadmium stress caused overproduction of H 2 O 2 in roots and leaves of pea seedlings. Cadmium-induced overproduction of H 2 O 2 caused a decrease in the pigment contents and increased lipid peroxidation. Application of EDTA at higher levels (81 and 200µM) increased Cd accumulation by pea plants. However, CA did not affect Cd accumulation by pea. Both EDTA and CA increased Cd-induced H 2 O 2 production and lipid peroxidation. Younger pea leaves showed more sensitivity to Cd stress compared to older leaves. Similarly, Cd toxicity was more pronounced in germinating seedlings than young seedlings. Moreover, Pearson correlation and principal component analysis (PCA) showed very interesting correlations between treatments and stress responses of germination and young seedlings as well as younger and older leaves. Based on multivariate analysis, it is proposed that the Cd toxicity to pea plants greatly vary with its growth stage and the maturity of organs (younger or older leaves)., (Copyright © 2018 Elsevier Inc. All rights reserved.)

The drug resistant bacteria and textile contaminations of water cause different sever health problem throughout the world. To overcome this issue, new environmental benign materials and methods are needed. Plant metabolites directed synthesis of nanoparticles is considered eco-friendly and easy in synthesis. Therefore, it was explicit for the synthesis of AgNPs. The prepared AgNPs were evaluated for antibacterial, antioxidant, photo-catalytic and electrochemical degradation properties as well as toxicity of degradation products on aquatic life. X-Ray Photoelectron Spectroscopy (XPS) has been used for analyzing the surface chemistry of prepared AgNPs. The particle size determines the interaction of nanoparticles with pathogens. Both Gram positive and negative bacteria (Escherichia coli and Staphylococcus areous) are used to determine the anti-microbial potency of the green synthesized AgNPs. The synthesized silver nanoparticles showed significant anti-bacterial applications against B. subtilus and S. aureus. The anti-oxidant applications of AgNPs also studied on comparison with vitamin C. The toxicity of the phenolic Azo dyes (PDA) has been studied against Fish, Daphnia and Green Algae. The electrode potential was studied in the electrochemical redox reaction of hydroxy phenol in aqueous media. Simple electrolyte was used to determine the current efficiency. For the stability of electrode multi cyclic voltammetry was also studied during redox reaction, which showed stability under the potential 0.4 to 0.2 V., (Copyright © 2018 Elsevier B.V. All rights reserved.)

The present study was conducted to explore arsenic (As) tolerance and phytostabilization potential of the two tree species, buttonwood (Conocarpus erectus) and eastern cottonwood (Populus deltoides). Both plant species were grown in pots and were exposed to various soil As levels (control, 5, 10, 15, and 20 mg kg -1 ). The plants were harvested after 9 months for the evaluation of growth parameters as well as root and shoot As concentrations. With increasing soil As levels, plant height stress tolerance index (PHSTI) was significantly decreased in both tree species, whereas root length stress tolerance index (RLSTI) and dry matter stress tolerance index (DMSTI) were not affected. Root and shoot As concentrations significantly increased in both tree species with increasing soil As levels. Translocation factor and bioconcentration factor were less than 1.0 for both plant species. This study revealed that both tree species are non-hyperaccumulators of As, but they could be used for phytostabilization of As-contaminated soils.

Synthesis of Nobel metal nanoparticles, play a key role in the field of medicine. Plants contain a substantial number of organic constituents, like phenolic compounds and various types of glycosides that help in synthesis of metal nanoparticles. Synthesis of metal nanoparticles by green method is one of the best and environment friendly methods. The major significance of the green synthesis is lack of toxic by-products produced during metal nanoparticle synthesis. The nanoparticles, synthesized by green method show various significant biological activities. Most of the research articles report the synthesized nanoparticles to be active against gram positive and gram negative bacteria. Some of these bacteria include Escherichia coli, Bacillus subtilis, Klebsiella pneumonia and Pseudomonas fluorescens. The synthesized nanoparticles also show significant antifungal activity against Trichophyton simii, Trichophyton mentagrophytes and Trichophyton rubrum as well as different types of cancer cells such as breast cancer cell line. They also exhibit significant antioxidant activity. The activities of these Nobel metal nano-particles mainly depend on the size and shape. The particles of small size with large surface area show good activity in the field of medicine. The synthesized nanoparticles are also active against leishmanial diseases. This research article explores in detail the green synthesis of the nanoparticles and their uses thereof., (Copyright © 2017 Elsevier B.V. All rights reserved.)

In this study, a novel immobilized TiO 2 /Ti film with exposed {001} facets was prepared via a facile one-pot hydrothermal route for the degradation of norfloxacin from aqueous media. The effects of various hydrothermal conditions (i.e., solution pH, hydrothermal time (H T ) and HF concentration) on the growth of {001} faceted TiO 2 /Ti film were investigated. The maximum photocatalytic performance of {001} faceted TiO 2 /Ti film was observed when prepared at pH 2.62, H T of 3 h and at HF concentration of 0.02 M. The as-prepared {001} faceted TiO 2 /Ti films were fully characterized by field-emission scanning electron microscope (FE-SEM), X-ray diffraction (XRD), high resolution transmission electron microscope (HR-TEM), and X-ray photoelectron spectroscopy (XPS). More importantly, the as-prepared {001} faceted TiO 2 /Ti film exhibited excellent photocatalytic performance toward degradation of norfloxacin in various water matrices (Milli-Q water, tap water, river water and synthetic wastewater). The individual influence of various anions (SO 4 2- , HCO 3 - , NO 3 - , Cl - ) and cations (K + , Ca 2+ , Mg 2+ , Cu 2+ , Na + , Fe 3+ ) usually present in the real water samples on the photocatalytic performance of as-prepared TiO 2 /Ti film with exposed {001} facet was investigated. The mechanistic studies revealed that • OH is mainly involved in the photocatalytic degradation of norfloxacin by {001} faceted TiO 2 /Ti film. In addition, norfloxacin degradation byproducts were investigated, on the basis of which degradation schemes were proposed.

This study reports the efficiency of gamma-ray irradiation to degrade quinolone antibiotic, norfloxacin, in aqueous solution. Laboratory batch experiments were conducted to determine the "pseudo-first" order degradation kinetics of norfloxacin in the concentration ranges of 3.4-16.1 mg L(-1) by gamma-ray irradiation. The dose constant was found to be dependent on the initial concentration of norfloxacin and gamma-ray irradiation dose rate (D r). The saturation of norfloxacin sample solutions with N2, air or N2O, and the presence of tert-butanol and 2-propanol showed that (•)OH played more crucial role in the degradation of norfloxacin. The second order rate constants of (•)OH, eaq (-), and (•)H with norfloxacin were calculated to be 8.81 × 10(9), 9.54 × 10(8), and 1.10 × 10(9) M(-1) s(-1), respectively. The effects of various additives including CO3 (2-), HCO3 (-), NO3 (-), NO2 (-), and thiourea and the pH of the medium on the degradation of norfloxacin were also investigated. Norfloxacin degradation was lower in surface water and wastewater than in ultrapure water. Several degradation byproducts of norfloxacin were identified from which the possible degradation pathway was proposed.

The present study elaborates the removal of endosulfan, an emerging water pollutant and potential carcinogenic, in aerated solution. The influence of Cl(-), NO3 (-), NO2 (-), CO3 (2-), HCO3 (-), SO3 (2-), and humic acid was assessed on the radiolytic degradation of endosulfan. A strong inhibition on the radiolytic degradation of endosulfan was observed in the presence of NO3 (-), NO2 (-), and SO3 (2-). Instead, a slight increase in the removal efficiency of endosulfan was observed at high concentrations of CO3 (2-) and HCO3 (-). The formation of CO3 (•-) in radiolytic degradation of endosulfan in the presence of CO3 (2-) and HCO3 (-) was demonstrated by adding SO3 (2-) that rapidly react with CO3 (•-). The results indicate that CO3 (•-) formed from the reactions of CO3 (2-) and HCO3 (-) and commonly found in natural water can play an important role in the degradation of endosulfan and other sulfur containing electron-rich compounds. The study showed faster degradation of endosulfan at lower concentration compared to high concentration and removal was found to follow pseudo-first-order kinetic. Endosulfan ether was found as the main degradation product and degradation pathway was found to be initiated at the S=O bond of endosulfan. The efficiency of gamma irradiation in the removal of endosulfan was examined in terms of formation of short chain organic acids and chloride ion accumulation.

The degradation of atrazine was investigated in aqueous solution by gamma-ray irradiation. 8.11 μM initial atrazine concentration could be completely removed in N₂ saturated solution by applying 3500 Gy radiation dose at a dose rate of 296 Gy h(-1). Significant removal of atrazine (i.e., 39.4%) was observed at an absorbed dose of 1184 Gy in air saturated solution and the removal efficiency was promoted to 50.5 and 65.4% in the presence of N₂O and N₂ gases, respectively. The relative contributions of hydrated electron, hydroxyl radical and hydrogen radical toward atrazine degradation were determined as ratio of observed dose constant (kobs) and found to be 5: 3: 1 for keaq(-): k·OH: kH·, respectively. The degradation efficiency of atrazine was 69.5, 55.6 and 37.3% at pH 12.1, 1.7 and 5.7, respectively. A degradation mechanism was proposed based on the identified degradation by-products by gas chromatography-mass spectrometry. Taking the relative contributions of oxidative and reductive species to atrazine degradation into account, reductive pathway proved to be a better approach for the radiolytic treatment of atrazine contaminated water., (Copyright © 2014 Elsevier B.V. All rights reserved.)

The gamma irradiation was investigated for potential removal of endosulfan sulfate, an emerging water pollutant and central nervous system disruptor. A removal efficiency of 99.5% of initially 1.30 μM endosulfan sulfate was observed at an absorbed dose of 1020 Gy. Aqueous electron (eaq(-)) was found to play primary role in the removal of endosulfan sulfate which was possibly due to greater reactivity of eaq(-) with endosulfan sulfate, considering the second-order rate constant of 8.1×10(9) and 3.4×10(10) M(-1) s(-1) for hydroxyl radical (·OH) and eaq(-), respectively, with endosulfan sulfate. The removal efficiency of endosulfan sulfate was affected by the pH of aqueous solution, with observed removal efficiency of 99.5%, 98.3% and 31.3% at pH 6.2, pH 10.0, and pH 2.6, respectively. The efficiency was also influenced by inorganic anions and humic acid in the order of nitrate>nitrite>bicarbonate>carbonate ≃ humic acid. The initial degradation rate increased while degradation constant decreased with increasing initial concentrations of endosulfan sulfate. The degradation pathways showed that oxidative pathway was initiated at the SO2 bond while reductive pathways at the chlorine attached to the ring of endosulfan sulfate. The mass balance showed removal of 98% chloride and 72% sulfate ions from endosulfan sulfate at an absorbed dose of 1020 Gy. The removal of endosulfan sulfate followed by subsequent loss of by-products under extended treatment showed that gamma irradiation is potential technique for the remediation of organic pollutants from a water environment., (Copyright © 2014. Published by Elsevier Ltd.)

This study aimed to assess the concentrations of heavy metals such as cadmium (Cd), chromium (Cr), copper (Cu), manganese (Mn), nickel (Ni), lead (Pb) and zinc (Zn) in the available foodstuffs (crops, milk and water), their bioaccumulation in human body and potential human health risks in Swat valley, northern Pakistan. Heavy metal concentrations in foodstuffs and human blood (adults (18-above) and children (1-12 years)) were analyzed using atomic absorption spectrometer. The results revealed high level of Mn in foodstuffs followed by Cr>Cu>Zn>Ni>Cd>Pb, which significantly increased the levels of heavy metals in the adult׳s blood as compared to that of children in the order of Cr>Zn>Mn>Ni>Pb>Cu>Cd. Principal component analysis showed that selected foodstuffs were the possible sources of metal contamination in human blood, while correlation analysis revealed that the concentrations of Cr, Cu, Mn, Ni, Pb and Zn in foodstuffs significantly correlated with that in human blood. Moreover, risk assessments for individual metals via foodstuffs were found within safe limits, except for Cd (HQ>1); Whereas, for aggregate multiple metals the risk was calculated as 3.97E+00 (HI>1), in which water and milk were perceived as the greater contributors (81 percent) to HI; while fruits, grains and vegetables contributed 5 percent each, and pulses 4 percent., (Copyright © 2014 Elsevier Inc. All rights reserved.)

The removal of endosulfan, an emerging water pollutant, from water was investigated using gamma irradiation based advanced oxidation and reduction processes (AORPs). A significant removal, 97% of initially 1.0 μM endosulfan was achieved at an absorbed dose of 1020 Gy. The removal of endosulfan by gamma-rays irradiation was influenced by an absorbed dose and significantly increased in the presence of aqueous electron (eaq(-)). However, efficiency of the process was inhibited in the presence of eaq(-) scavengers, such as N2O, NO3(-), acid, and Fe(3+). The observed dose constant decreased while radiation yield (G-value) increased with increasing initial concentrations of the target contaminant and decreasing dose-rate. The removal efficiency of endosulfan II was lower than endosulfan I. The degradation mechanism of endosulfan by the AORPs was proposed showing that reductive pathways involving eaq(-) started at the chlorine attached to the ring while oxidative pathway was initiated due to attack of hydroxyl radical at the SO bond. The mass balance showed 95% loss of chloride from endosulfan at an absorbed dose of 1020 Gy. The formation of chloride and acetate suggest that gamma irradiation based AORPs are potential methods for the removal of endosulfan and its by-products from contaminated water., (Copyright © 2014. Published by Elsevier B.V.)

This study explored the efficiency of UV-C-based advanced oxidation processes (AOPs), i.e., UV/S2O8(2-), UV/HSO5(-), and UV/H2O2 for the degradation of endosulfan, an organochlorine insecticide and an emerging water pollutant. A significant removal, 91%, 86%, and 64%, of endosulfan, at an initial concentration of 2.45 μM and UV fluence of 480 mJ/cm(2), was achieved by UV/S2O8(2-), UV/HSO5(-), and UV/H2O2 processes, respectively, at a [peroxide]0/[endosulfan]0 molar ratio of 20. The efficiency of these processes was, however, inhibited in the presence of radical scavengers, such as alcohols (e.g., tertiary butyl alcohol and isopropyl alcohol) and natural organic matter (NOM). The inhibition was also influenced by common inorganic anions in the order of nitrite > bicarbonate > chloride > nitrate ≈ sulfate. The observed pseudo-first-order rate constant decreased while the degradation rate increased with increasing initial concentration of the target contaminant. The degradation mechanism of endosulfan by the AOPs was evaluated revealing the main by-product as endosulfan ether. Results of this study suggest that UV-C-based AOPs are potential methods for the removal of pesticides, such as endosulfan and its by-products, from contaminated water., (Copyright © 2013 Elsevier B.V. All rights reserved.)