Utilizing sludge-based activated carbon for targeted leachate mitigation in wastewater treatment.

Activated carbon (AC) based adsorbents derived from waste sludge were utilized to remediate mixed contaminants in wastewater as an integrated waste-to-resource approach promoting a paradigm shift in management of refuse sludge and wastewater. This review specifically focuses on the remediation of constituents of landfill leachate by sludge-based activated carbon (SBAC). The adsorption effectiveness of SBAC for the exclusion of leachate characters including heavy metals, phenols, dyes, phosphates, and phosphorus were explored with regard to modifiers such as pH, temperature, properties of the adsorbent including functional groups, initial doses of absorbent and adsorbate, and duration of exposure to note the impact of each parameter on the efficiency of adsorption of the sludge adsorbent. Through the works of various researchers, it was noted that the properties of the adsorbent, pH and temperature impact the working of SBACs. The pH of the adsorbent by influencing the functional groups. Temperature was expected to have a paramount effect on the adsorption efficiency of the SBACs. The importance of the regeneration and recycling of the adsorbents as well as their leachability is highlighted. Sludge based activated carbon is recommended as a timely, resource-efficient, and sustainable approach for the remediation of wastewater.

An eco-friendly approach on green synthesis, bio-engineering applications, and future outlook of ZnO nanomaterial: A critical review.

Synthesizing ZnO nanostructures ranging from 1 nm to 4 nm confines the electron cloud and exhibits a quantum effect generally called as quantum confinement effect attracting many researchers in the field of electronics and optics. ZnO nanostructures are used in medical applications to formulate antioxidant, antibacterial, antifungal, anti-inflammatory, wound healing, and anti-diabetic medications. This work is a comprehensive study of green synthesis of ZnO nanomaterials using different biological sources and highlights different processes able to produce nanostructures including nanowires, nanorods, nanotubes and other nano shapes of ZnO nanostructures. Different properties of ZnO nanostructures and their targeted bioengineering applications are also described. The strategies and challenges of the eco-friendly approach to enhance the application span of ZnO nanomaterials are also summarized, with future prospects for greener design of ZnO nanomaterials are also suggested.

Design of tropinium-functionalized anion exchange membranes for acid recovery via diffusion dialysis process.

Diffusion dialysis (DD) process utilizing anion exchange membranes (AEMs) is an environmentally-friendly and energy-efficient technology. From acidic wastewater, DD is needed for acid recovery. This research reports the development of a series of dense tropinium-functionalized AEMs via solution casting method. Fourier Infrared transform (FTIR) spectroscopy verified the successful preparation of AEMs. The developed AEMs exhibited a dense morphology, featuring 0.98-2.42 mmol/g of ion exchange capacity (IEC), 30-81% of water uptake (WR) and 7-32% of linear swelling ratio (LSR). They displayed exceptional mechanical, thermal and chemical stability and were employed for acid waste treatment from HCl/FeCl2 mixtures via DD process. AEMs possessed 20 to 59 (10-3 m/h) and 166 to 362 of acid diffusion dialysis coefficient (UH+) and separation factor (S) respectively at 25 °C. Compared to DF-120 commercial membrane (UH+ = 0.004 m/h, S = 24.3), their DD efficiency was improved under identical experimental conditions.

Assessment of the biochemical methane potential of mono- and co-digested dairy farm wastes.

This study aimed to evaluate the methane potential of mono- and co-digested dairy farm wastes. The tested substrates included manure from lactating, dry, and young cows, as well as waste milk and feed waste. The highest methane yield was achieved from the lactating cow manure, which produced an average of 412 L of CH4 kg-1 volatile solids, followed by young and dry cow manures (332 and 273 L of CH4 kg-1 volatile solids, respectively). Feed and milk yielded an average of 325 and 212 L of CH4 kg-1 volatile solids, respectively. Co-digesting the manures from lactating and young cows with feed improved methane production by 7%. However, co-digesting the dry cow manure with feed achieved only 85% of the calculated methane yield. Co-digesting manure and milk at a ratio of 70:30 enhanced the methane potential from lactating, dry, and young cow manures by 19, 30, and 37%, respectively. Moreover, co-digesting lactating, dry, and young cow manures with milk at a ratio of 30:70 enhanced the methane yield by 60, 30, and 88%, respectively. The cumulative methane production of all samples was accurately described using the Gompertz model with a maximum error of 10%. Carbohydrates contributed the most to methane potential, while proteins and lipids were limiting.

Waste to energy potential in middle income countries of MENA region based on multi-scenario analysis for Kafr El-Sheikh Governorate, Egypt.

The environmental risks of traditional waste disposal methods, together with the resource and energy value of waste, had established the foundation for waste-to-energy (WTE) technologies. WTE is rarely implemented in developing countries, mostly due to the lack of knowledge and experience under their specific local conditions. The present research investigates the feasibility of WTE strategies in middle income developing countries of the Middle East and North Africa (MENA) region. Multiple waste management scenarios, involving incineration and anaerobic digestion, were evaluated based on energy, economic, and environmental parameters. A multi-criteria assessment was conducted for the Governorate of Kafr El-Sheikh (Egypt); a 3.2-million rural-urban agro-industrial population with socio-economic and demographic features similar to those of the selected MENA countries. The actual waste generation rates and characteristics of Kafr El-Sheikh were measured through a comprehensive field study. It was found that anaerobic digestion with recycling is the optimum strategy for Kafr El-Sheikh, with annual energy potential of 1170-kWh per ton of waste and net economic savings of 6.5 million USD. This optimum waste management scenario was extended to the selected MENA countries to investigate potential benefits of shifting to WTE-based waste management strategies. The total annual energy production was estimated to be 103,000-GWh, which translates to 17% of the total energy consumption. Moreover, greenhouse gas emissions were reduced by around 98,500-Gg CO2 annually, which represents around 6.5% of the total annual CO2 footprint generated by the selected countries. Furthermore, the overall economic benefits ranged between -12 and 200 million USD for the selected countries.

Simultaneous Determination of Pharmaceuticals by Solid-phase Extraction and Liquid Chromatography-Tandem Mass Spectrometry: A Case Study from Sharjah Sewage Treatment Plant.

The present work describes the optimization and validation of a highly selective and sensitive analytical method using solid phase extraction and liquid chromatography tandem mass spectrometry (SPE LC-MS/MS) for the determination of some frequently prescribed pharmaceuticals in urban wastewater received and treated by Sharjah sewage treatment plant (STP). The extraction efficiency of different SPE cartridges was tested and the simultaneous extraction of pharmaceuticals was successfully accomplished using hydrophilic-lipophilic-balanced reversed phase Waters® Oasis HLB cartridge (200 mg/ 6 mL) at pH 3. The analytes were separated on an Aquity BEH C18 column (1.7 µm, 2.1 mm × 150 mm) using gradient elution and mass spectrometric analysis were performed in multiple reactions monitoring (MRM) selecting two precursor ions to produce ion transition for each pharmaceutical using positive electrospray ionization (+ESI) mode. The correlation coefficient values in the linear calibration plot for each target compound exceeded 0.99 and the recovery percentages of the investigated pharmaceuticals were more than 84%. Limit of detection (LOD) varied between 0.1⁻1.5 ng/L and limit of quantification (LOQ) was 0.3⁻5 ng/L for all analytes. The precision of the method was calculated as the relative standard deviation (RSD%) of replicate measurements and was found to be in the ranges of 2.2% to 7.7% and 2.2% to 8.6% for inter and intra-day analysis, respectively. All of the obtained validation parameters satisfied the requirements and guidelines of analytical method validation.

Spatio-temporal analysis of urban growth and its impact on floods in Ajman City, UAE.

The negative consequences of urbanisation have been recently recognised despite the social and economic benefits it provides to the community. Effects of urbanisation include increases in surface runoff, frequency and magnitude of floods and urban water harvesting capacity. Accordingly, this study utilised multi-spectral and multi-resolution satellite images combined with field data to conduct a quantitative assessment of the impact of urbanisation on urban flooding for the period of 1975-2015 in Ajman City, United Arab Emirates (UAE). Results showed that urban areas in the city have increased by approximately 12-fold over the period 1975-2015, whilst the population increased by approximately 16-fold. Owing to a substantial increase in urbanisation (as impervious areas expanded), minimum precipitation to generate runoff in built areas dropped from approximately 16.37 mm in 1975 to approximately 13.3 mm in 2015, which caused a substantial increase in the surface runoff. To visualise the flooding potential, urban flooding maps were generated using a well-established decision analysis technique called Analytical Hierarchy Process. The latter adopted three thematic factors, namely excess rain, elevation and slope. Flooding potential was then found to have increased substantially, specifically in the downtown area. Finally, this study is expected to contribute highly to flood protection and sustainable urban storm water management in Ajman City.

Macro and micro geo-spatial environment consideration for landfill site selection in Sharjah, United Arab Emirates.

Waste management involves various procedures and resources for proper handling of waste materials in compliance with health codes and environmental regulations. Landfills are one of the oldest, most convenient, and cheapest methods to deposit waste. However, landfill utilization involves social, environmental, geotechnical, cost, and restrictive regulation considerations. For instance, landfills are considered a source of hazardous air pollutants that can cause health and environmental problems related to landfill gas and non-methanic organic compounds. The increasing number of sensors and availability of remotely sensed images along with rapid development of spatial technology are helping with effective landfill site selection. The present study used fuzzy membership and the analytical hierarchy process (AHP) in a geo-spatial environment for landfill site selection in the city of Sharjah, United Arab Emirates. Macro- and micro-level factors were considered; the macro-level contained social and economic factors, while the micro-level accounted for geo-environmental factors. The weighted spatial layers were combined to generate landfill suitability and overall suitability index maps. Sensitivity analysis was then carried out to rectify initial theoretical weights. The results showed that 30.25% of the study area had a high suitability index for landfill sites in the Sharjah, and the most suitable site was selected based on weighted factors. The developed fuzzy-AHP methodology can be applied in neighboring regions with similar geo-natural conditions.

Solar-matched S-scheme ZnO/g-C3N4 for visible light-driven paracetamol degradation.

In pursuit of an efficient visible light driven photocatalyst for paracetamol degradation in wastewater, we have fabricated the ZnO/g-C3N4 S-Scheme photocatalysts and explored the optimal percentage to form a composite of graphitic carbon nitride (g-C3N4) with zinc oxide (ZnO) for enhanced performance. Our study aimed to address the urgent need for a catalyst capable of environmentally friendly degradation of paracetamol, a common pharmaceutical pollutant, using visible light conditions. Here, we tailored the band gap of a photocatalyst to match solar radiation as a transformative advancement in environmental catalysis. Notably, the optimized composite, containing 10 wt.% g-C3N4 with ZnO, demonstrated outstanding paracetamol degradation efficiency of 95% within a mere 60-min exposure to visible light. This marked enhancement represented a 2.24-fold increase in the reaction rate compared to lower wt. percentage composites (3 wt.% g-C3N4) and pristine g-C3N4. The exceptional photocatalytic activity of the optimized composite can be attributed to the band gap narrowing that closely matched the maximum solar radiation spectrum. This, coupled with efficient charge transfer mechanisms through S-scheme heterojunction formation and an abundance of active sites due to increased surface area and reduced particle size, contributed to the remarkable performance. Trapping experiments identified hydroxyl radicals as the primary reactive species responsible for paracetamol photoreduction. Furthermore, the synthesized ZnO/g-C3N4 composite exhibited exceptional photostability and reusability, underscoring its practical applicability. Thus, this research marks a significant stride towards the development of an effective and sustainable visible light photocatalyst for the removal of pharmaceutical contaminants from aquatic environments.

Assessment of elemental chemistry, spatial distribution, and potential risks of road-deposited dusts in Sharjah, United Arab Emirates.

Road dust is a major source of pollution in the environment, carrying different pollutants, including heavy metals and metalloids, from one location to another. This study assesses the concentrations of eight heavy metals and one metalloid (Zn, Pb, Mn, Fe, Cr, Cu, Cd, Ni, and As) in dust samples collected from sixty-eight streets of Sharjah, United Arab Emirates using ICP-OES, as well as investigates their effects on both the environment and humans. Mean concentrations of the elements in µg/g across the sites were 392 ± 46 (Zn), 68.28 ± 11.3 (Pb), 1437 ± 67 (Mn), 39,481 ± 4611 (Fe), 460 ± 31 (Cr), 150 ± 44 (Cu), 1.25 ± 0.65 (Cd), 856 ± 72 (Ni), and 0.97 ± 0.28 (As). The Cdeg and ERI calculated from the study were 54.79 and 573, respectively, suggesting varying pollution levels. The highest contributions were from Ni, Cd, Zn, Cu, Cr, and Pb, especially in areas with heavy traffic. The non-carcinogenic risk assessments were generally low for the three routes of exposure, except HQoral that was slightly higher for children. Similarly, none of the elements exhibited any carcinogenic risk except chromium. Overall, the cancer risk is considered low. In view of the limited studies from UAE in relation to the metal content of road-deposited dusts, the current study serves as novel knowledge, especially in the context of geographical areas with a higher occurrence of sandstorms and the presence of particulate matter. The study also adds to the global understanding of the contribution of street dust to environmental pollution and its implications for human health.

Smart optical sensing of multiple antibiotic residues from wastewater effluents with ensured specificity using SERS assisted with multivariate analysis.

Surface-enhanced Raman spectroscopy offers great potential for rapid and highly sensitive detection of pharmaceuticals from environmental sources. Herein, we investigated the feasibility of label-free sensing of antibiotic residues from wastewater effluents with high specificity by combining with multivariate analysis. Highly ordered silver nanoarrays with ∼34 nm roughness have been fabricated using a cost-effective electroless deposition technique. As-fabricated Ag arrays showed superior LSPR effects with an enhancement factor of 8 × 107. Excellent reproducibility has also been noticed with RSD values within 11%, whilst the sensor showed good stability and reusability characteristics for being used as a low-cost and reusable sensor. SERS studies demonstrated that antibiotics-spiked wastewater effluents can be detected with high efficiency in a label-free method. The molecular fingerprint bands of antibiotics such as sulfamethoxazole, sulfadiazine, and ciprofloxacin were well analyzed in effluent, tap, and deionized water. It has been found that antibiotics can be detected near picomolar levels; meanwhile, liquid chromatography-mass spectrometry (LC-MS) exhibited a detection limit within nanomolar concentrations only. Furthermore, the specificity of SERS sensing has been further analyzed using a multivariate analysis method, principal component analysis followed by linear discriminant analysis (PCA-LDA); which showed prominent discrimination to distinguish each antibiotic residue from wastewater effluents. The current study presented the potential of Ag nanoarray sensors for rapid, highly specific, and cost-effective analysis of pharmaceutical products for environmental remediation applications.

Adsorption of Eosin B from Wastewater onto the Prepared Porous Anion Exchange Membrane.

This research describes the fabrication of the porous trimethylamine (TMA)-grafted anion exchange membrane (AEM) over a phase inversion process. The synthesis of the generated AEM was verified using Fourier transform infrared (FTIR) spectroscopy. The fabricated porous AEM showed 240% water uptake (WR), 1.45 mg/g ion exchange capacity (IEC), and a 9.0% linear expansion ratio (LER) at 25 °C. It exhibited a porous structure and higher thermal stability. It was utilized to remove eosin B (EB) from wastewater via the process of adsorption. The adsorption capacity of EB increased with time and the starting concentration of EB while decreasing with temperature and the AEM dosage. Adsorption isotherm investigation results showed that EB adsorption onto the porous AEM followed the Langmuir isotherm because the value of correlation coefficient (R2 = 0.992) was close to unity. Because the correlation coefficient was close to one, it was determined through adsorption kinetic experiments that the adsorption of EB on the produced porous AEM was suitable for a pseudo-second-order model. Thermodynamic study about process of EB adsorption on the porous AEM revealed that there was an exothermic (ΔH° = -16.60 kJ/mol) and spontaneous process.

Isotherms, kinetics and thermodynamic mechanism of methylene blue dye adsorption on synthesized activated carbon.

The treatment of methylene blue (MB) dye wastewater through the adsorption process has been a subject of extensive research. However, a comprehensive understanding of the thermodynamic aspects of dye solution adsorption is lacking. Previous studies have primarily focused on enhancing the adsorption capacity of methylene blue dye. This study aimed to develop an environmentally friendly and cost-effective method for treating methylene blue dye wastewater and to gain insights into the thermodynamics and kinetics of the adsorption process for optimization. An adsorbent with selective methylene blue dye adsorption capabilities was synthesized using rice straw as the precursor. Experimental studies were conducted to investigate the adsorption isotherms and models under various process conditions, aiming to bridge gaps in previous research and enhance the understanding of adsorption mechanisms. Several adsorption isotherm models, including Langmuir, Temkin, Freundlich, and Langmuir-Freundlich, were applied to theoretically describe the adsorption mechanism. Equilibrium thermodynamic results demonstrated that the calculated equilibrium adsorption capacity (qe) aligned well with the experimentally obtained data. These findings of the study provide valuable insights into the thermodynamics and kinetics of methylene blue dye adsorption, with potential applications beyond this specific dye type. The utilization of rice straw as an adsorbent material presents a novel and cost-effective approach for MB dye removal from wastewater.

Removal of phosphate from water using six Al-, Fe-, and Al-Fe-modified bentonite adsorbents.

This study was part of a larger effort that involves evaluating alternatives to upgrading secondary treatment systems in the United Arab Emirates for the removal of nutrients. In this study, six modified bentonite (BNT) phosphate adsorbents were prepared using solutions that contained hydroxy-polycations of aluminum (Al-BNT), iron (Fe-BNT), and mixtures of aluminum and iron (Al-Fe-BNT). The adsorption kinetics and capacities of the six adsorbents were evaluated, and the adsorbents were used to remove phosphorus from synthetic phosphate solutions and from treated wastewater. The experimental adsorption kinetics results were well represented by the pseudo-second-order kinetic model, with R(2) values ranging from 0.99 to 1.00. Similarly, the experimental equilibrium adsorption results were well represented by the Freundlich and Langmuir isotherms, with R(2) values ranging from 0.98 to 1.00. The adsorption capacities of the adsorbents were dependent on the BNT preparation conditions; the types, quantities and combination of metals used; BNT particle size; and adsorption pH. The Langmuir maximum adsorption capacities of the six adsorbents ranged from 8.9-14.5 mg P/g-BNT. The results suggested that the BNT preparations containing Fe alone or in combination with Al achieved higher adsorption capacities than the preparations containing only Al. However, the Al-BNT preparations exhibited higher adsorption rates than the Fe-BNT preparation. Three of the six adsorbents were used to remove phosphate from secondarily treated wastewater samples, and the removal results were comparable to those obtained using synthetic phosphate solutions. The BNT adsorbents also exhibited adequate settling characteristics and significant regeneration potential.

Novel composites of activated carbon and layered double oxide for the removal of sulfate from synthetic and brackish groundwater.

Sulfate (SO42-) is a major water and environmental concern that causes severe diarrhea, death of invertebrates and plant species, and clogging of industrial pipes. In the current work, treatment of SO42- from synthetic and real groundwater having 3901 mg(SO42-)/L was investigated for the first time using Zn-Al and Mg-Al layered double oxides doped granular activated carbon (GAC/Mg-Al LDO and GAC/Zn-Al LDO). The co-precipitation method was followed to synthesize the GAC/LDO composites using an Mg or Zn to Al molar ratio of 3:1. The GAC/Mg-Al LDO possessed a higher specific surface area (323.9 m2/g) compared to GAC/Zn-Al LDO (195.1 m2/g). The GAC/Mg-Al LDO demonstrated more than 99% removal of SO42- from synthetic water, while it was 50.9% for GAC/Zn-Al LDO and less than 1% for raw GAC at an initial concentration of 50 mg/L. The GAC/Mg-Al LDO was selected for further batch experiments and modeling investigation. The equilibrium data followed the Redlich-Peterson and Langmuir models with determination coefficients of 0.943 and 0.935, respectively. The maximum Langmuir adsorption capacity was 143.5 mg/g. In the real groundwater adsorption study, the screening experiment revealed high selectivity towards SO42- with 62% removal efficiency. The optimum dosage was found to be 50 g/L with an uptake capacity of 61.5 mg/g. The kinetic data of SO42- removal from synthetic and brackish water were in excellent agreement with the pseudo-second order model, and the equilibrium was attained in 5 h. Accordingly, it can be concluded that the GAC/Mg-Al LDO is an efficient material for treating SO42- from real groundwater and can be utilized as a pretreatment unit for high sulfate water resources.

Application of QPPO/PVA based commercial anion exchange membrane as an outstanding adsorbent for the removal of Eosin-B dye from wastewaters.

Commercially available QPPO/PVA based anion exchange membrane (AEM) BIII was to inquire the percentage discharge of anionic dye Eosin-B (EB) at terrain temperature from wastewater. The impact of EB initial concentration, membrane dosage, ionic strength, contact time and temperature on EB percentage removal was contemplated. The EB percentage removal was increased from 22 to 99.56% and 38.15-99.56% with contact time and membrane dosage respectively while decreased from 99.56 to 29%, 99.56 to 54.61% and 99.56 to 92.22% with enhancing initial concentration of EB, ionic strength and temperature respectively. Nonlinear isotherm models were utilized to demonstrate EB adsorption onto AEM BIII. Attained results exhibited that nonliner Freundlich isotherm model best fitted to EB adsorption onto AEM BIII. For EB adsorption onto AEM BIII, adsorption kinetics were inquired in detail by using several kinetic models but EB adsorption nicely fitted to pseudo-second-order kinetics. Similarly thermodynamic analysis was performed and results pointed to an exothermic adsorption of EB onto AEM BIII. The membrane could be reused for four concecutive cycles with loosing its efficiency.

Oxidized carbide-derived carbon as a novel filler for improved antifouling characteristics and permeate flux of hybrid polyethersulfone ultrafiltration membranes.

Polyethersulfone (PES) is a widely used polymer for ultrafiltration (UF) membrane fabrication. In the current study, carbide-derived carbon (CDC) oxidized by acid treatment was utilized as a filler to fabricate a novel PES composites UF membranes. The successful oxidation of CDC was validated from presence of oxygen containing functional groups and improved oxygen content, from 5.08 at.% for CDC to 26.22 at.% for oxidized CDC (OCDC). The OCDC PES UF membranes were prepared at different loadings of OCDC between 0.5 and 3.0 wt%. The membrane porosity, pore size and surface free energy found to be improved while a noticeable reduction in water contact angle was observed with OCDC loading implying the improved hydrophilicity of PES membranes. Consequently, the pure water flux found to improve from 151.6 to 569.6 (L/(m2. h)) for the 3.0 wt% modified OCDC membrane (M-3) which is 3.8 folds of the bare PES membrane. The antifouling characteristics were evaluated by humic acid (HA) filtration. The results revealed a significant enhancement in HA rejection with OCDC loading, the highest rejection was 96.8% for M-3 membrane. Additionally, the adsorption capacity of OCDC modified membranes found to decrease with OCDC loading indicating improved rejection of HA from the membrane surface. Moreover, M-3 demonstrated the maximum flux recovery ratio (FRR) of 92.3%. Reusability of the fabricated membranes was evaluated by deionized water/humic acid cycling filtration. The FRR was higher than 86.7% over three cycles of pure water/HA filtration for 140 min, indicated the excellent stability and reusability of the membranes. Overall, the OCDC was an effective filler for enhancing the PES UF membranes antifouling and permeability properties.

Tumor micro-environment sensitive release of doxorubicin through chitosan based polymeric nanoparticles: An in-vitro study.

Conventional chemotherapy poses toxic effects to healthy tissues. A therapeutic system is thus required that can administer, distribute, metabolize, and excrete medicine from human body without damaging healthy cells. This is possible by designing a therapeutic system that can release drug at specific target tissue. In current work, novel chitosan (CS) based polymeric nanoparticles (PNPs) containing N-isopropyl acrylamide (NIPAAM) and 2-(di-isopropyl amino) ethyl methacrylate (DPA) are designed. The presence of available functional groups i.e. OH- (3262 cm-1), -NH2 (1542 cm-1), and CO (1642 cm-1), was confirmed by Fourier Transform Infra-red Spectrophotometry (FTIR). The surface morphology and average particle size (175 nm) was determined through Scanning Electron Microscope (SEM). X-Ray Diffractometry (XRD) studies confirmed the amorphous nature and excellent thermal stability of PNPs up to 100 °C with only 2.69% mass loss was confirmed by Thermogravimetric analysis (TGA). The pH sensitivity of such PNPs for release of encapsulated doxorubicin at malignant site was investigated. The encapsulation efficiency of PNPs was 89% (4.45 mg/5 mg) for doxorubicin (a chemotherapeutic) measured by using UV-Vis Spectrophotometer. The drug release profile of loaded PNPs was 88% (3.92 mg/4.45 mg) at pH 5.3, in 96 h. PNPs with varying DPA concentration can effectively be used to deliver chemotherapeutic agents with high efficacy.

Experimental design by response surface methodology for efficient cefixime uptake from hospital effluents using anion exchange membrane.

The excessive use of antibiotics and their ultimate routes to the environment have prompted the drug resistance, which is becoming a major ecological issue. In this work, we have evaluated the performance of quaternary ammonium poly (2, 6-dimethyl-1,4-phenylene oxide) and polyvinyl alcohol (QPPO/PVA) based anion exchange membrane against cefixime (a third generation cephalosporin antibiotic) present in hospital effluents. The membrane's surface morphology was studied through scanning electron microscopy. The optimization of experimental parameters through Response Surface Methodology helped to evaluate the inter parameter dependence and predict maximum uptake capacity (qe). The speculated value of qe (6.72 mg g-1) obtained through central composite design was close to the experimental value of 7.01 mg g-1 with percent relative error of 4.31%. Further, the evaluation of experimental data using isotherms (Langmuir and Freundlich) and kinetic models (pseudo-first-order and second-order) proposed that the interactions between cefixime and the membrane were physisorptive in nature. The intra-day and inter-day assays exhibited lower %RSD values of 0.4% (n = 5) and 0.3% (n = 5). Furthermore, a percentage recovery of 98.2% (n = 9) and limit of detection 1 × 10-5 µg mL-1 was observed. The chromatogram of the treated water samples presented only negligible amount of cefixime indicating a great potential of QPPO/PVA membrane for the removal of cefixime from real water samples. The membrane could be regenerated for three consecutive cycles without any prominent loss in efficiency.

Molecularly imprinted ormosil as a sorbent for targeted dispersive solid phase micro extraction of pyriproxyfen from strawberry samples.

Novel molecularly imprinted organically modified silica was prepared by reacting acrylamide and 3-(tri-methoxysilyl) propyl methacrylate followed by condensation and hydrolysis with tetraethyl ortho-silicate for the determination of pyriproxyfen. The sorbent proved to be highly selective for the template molecule, pyriproxyfen. The characterization of sorbent was carried out using SEM, BET and TGA. The prominent peaks in FTIR at 3700 cm-1 and 1071 cm-1 confirmed the stretching of amide group's N-H and Si-O-Si bond linkage of MIOrmosil. The pseudo-first-order model (R2 0.99) described the adsorption kinetics of the MIOrmosil, whereas among adsorption isotherms, Freundlich model showed the best fit (R2 0.99). The molecularly imprinted silica was applied for the determination of target analytes from strawberries sample using dispersive solid-phase micro extraction (DSPME) followed by high-performance liquid chromatography (HPLC). The LOD (4.93 x10-5 µg mL-1) and LOQ (1.49 x10-4 µg m-1) values were calculated by signal to noise ratio through HPLC. Results show that the maximum binding capacity and percentage recovery values of MIOrmosil were 13 mg g-1 (n = 5) and 97.3% respectively.