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The rising population is increasing food demand, yet actual crop production is limited by the poor efficiency of classical fertilizers. In particular, only about 40–60% of fertilizer nitrogen, 15–20% of phosphorus and 50–60% of potassium are used by crop plants, the rest ending polluting the environment. Nanofertilizers are promising alternatives. Here, we review plant nutrients, synthesis of zinc oxide nanoparticles, encapsulation of nanoparticles in fertilizers, and effect on plants.

Polymer materials are vulnerable to damages, failures, and degradations, making them economically unreliable. Self-healing polymers, on the other hand, are multifunctional materials with superior properties of autonomic recovery from physical damages. These materials are suitable for biomedical and tissue engineering in terms of cost and durability. Schiff base linkages-based polymer materials are one of the robust techniques owing to their simple self-healing mechanism. These are dynamic reversible covalent bonds, easy to fabricate at mild conditions, and can self-reintegrate after network disruption at physiological conditions making them distinguished. Here we review self-healing polymer materials based on Schiff base bonds. We discuss the Schiff base bond formation between polymeric networks, which explains the self-healing phenomenon. These bonds have induced 100% recovery in optimal cases.

Engineered materials are crucial for the higher efficiency of supercapacitors. Current work presents roughly shaped spherical NiFe2O4 nanoparticles dispersed in the SiO2 matrix NiFe2O4/SiO2 as a newfangled electrode material for supercapacitors with remarkable performance. Designing the NiFe2O4/SiO2 nanostructure with a sol-gel method followed by the Stober method to grow silica has instigated NiFe2O4/SiO2 as dynamic material with higher electrochemical activity. Physicochemical aspects of NiFe2O4/SiO2 nanostructures are evaluated using Fourier-transform infrared spectroscopy, X-ray diffraction, scanning electron microscopy, and transmission electron microscopy analysis. The electrochemical activity is evaluated by cyclic voltammetry (CV) and galvanostatic charge-discharge (GCD) representing the comparable efficiency and reversibility of the electrode materials. The prepared electrode shows a capacitance of 925 F/g (154.1 mAh/g or 555 C/g) at 1 A/g, with 95.5% capacitance retention after 5000 cycles at 20 mA/cm2. The improved electrochemical performance of the NiFe2O4/SiO2 electrode can be subjected to prompt diffusion process provided by NiFe2O4/SiO2 and enhanced redox reactions owing to the high surface area. The mentioned features decrease the total impedance of the electrodes as suggested by electrochemical impedance spectroscopy (EIS).

Graphical abstract, Highlights • Taxonomic identification of a native silver-resistant bacterial strain. • Synthesis of silver nanoparticles (AgNPs) by the green method. • Characterization of purified AgNPs by spectroscopic and imaging techniques. • Measurement of antibacterial activity of AgNPs against human pathogens. • Estimation of anticancer potential of AgNPs against liver cancer cell line., Green nanomaterials have gained much attention due to their potential use as therapeutic agents. The present study investigated the production of silver nanoparticles (AgNPs) from a silver-resistant Bacillus safensis TEN12 strain, which was isolated from metal contaminated soil and taxonomically identified through 16S rRNA gene sequencing. The formation of AgNPs in bacterial culture was confirmed by using UV–vis spectroscopy with an absorption peak at 426.18 nm. Fourier transform infrared (FTIR) spectroscopy confirmed the involvement of capping proteins and alcohols for stabilization of AgNPs. Moreover, X-ray diffraction analysis (XRD), scanning and transmission electron microscopy (SEM and TEM) confirmed the crystalline nature and spherical shape of AgNPs with particle size ranging from 22.77 to 45.98 nm. The energy dispersive X-ray spectroscopy (EDX) revealed that 93.54% silver content is present in the nano-powder. AgNPs showed maximum antibacterial activity (20.35 mm and 19.69 mm inhibition zones) at 20 µg mL−1 concentration against Staphylococcus aureus and Escherichia coli, respectively and significantly reduced the pathogen density in broth culture. Furthermore, AgNPs demonstrated significant anticancer effects in the human liver cancer cell line (HepG2) in MTT assay, whereas, no cytotoxic effects were demonstrated by AgNPs on normal cell line (HEK293). The present study suggests that the biogenic AgNPs may substitute chemically synthesized drugs with wider applications as antibacterial and anticancer agents.

5-Fluorouracil (5-FU) being a mainstream anticancer drug is under keen and detailed investigation for prodrugs formulations in order to minimize the associated side effects. Cocrystallization of 5-FU is an innovative technique for the synthesis of 5-FU prodrugs to improve its anticancer effectiveness. The present study is based on the synthesis of 5-FU supramolecular synthons with four coformers: succinic acid, cinnamic acid, malic acid, and benzoic acid utilizing acetone as a solvent. Solid state grinding followed by a slow evaporation solution method was applied. Colorless clear crystals were obtained in all the cases. The cocrystal formation was supported with the help of Fourier transform infrared (FTIR) spectroscopy and powder X-ray diffraction (PXRD). Through FTIR, the main peaks of interest in the spectrum of 5-FU were N–H (3409.02 cm–1) and carbonyl group (1647.80 cm–1), which were prominently shifted in all spectra of the cocrystals demonstrating the replacement as well as the development of already present interactions with the new ones. For 5-FU–cinnamic acid cocrystals, the anticipated peaks were observed at 1673.13 cm–1 (−C═O) and 3566.89 cm–1 (N–H) manifesting a significant change in comparison to 5-FU. Furthermore, with the help of PXRD characterization, the representative peak of 5-FU was recorded at 2θ = 28.80°. The shifting of this specific peak and development of many new ones in the spectra of cocrystals proved the development of new structural entities. Finally, the anticancer activity of all cocrystals was evaluated in comparison to that of API. All cocrystals manifest significantly greater growth inhibition potential than the main active pharmaceutical ingredient. 5-FU–Cinnamic acid (3C) was the one that proved to be the most potent anticancer agent at all four concentrations: 4.82% (12 μg/mL), 34.21% (25 μg/mL), 55.08% (50 μg/mL), and 67.29% (100 μg/mL). In short, this study proved to be a true example to enhance the anticancer potential of 5-FU following fairly easy fabrication requirements of the cocrystallization phenomenon. After the successful synthesis of these supramolecular synthons and subsequent enhancement of growth inhibition potential of 5-FU, these cocrystals can further be evaluated for in vivo trials and membrane crossing potentials in the future.

Membrane-based gas separation has a great potential for reducing environmentally hazardous carbon dioxide (CO

Biogas up-gradation is a useful method to control CO

Currently, the global agriculture productivity is heavily relied on the use of chemical fertilizers. However, the low nutrient utilization efficiency (NUE) is the main obstacle for attaining higher crop productivity and reducing nutrients losses from these fertilizers to the environment. Coating fertilizer with micronutrients and biopolymer can offer an opportunity to overcome these fertilizers associated problems. Here, we coated urea with zinc sulphate (ZnS) and ZnS plus molasses (ZnSM) to control its N release, decrease the ammonia (NH3) volatilization and improve N utilization efficiency by sunflower. Morphological analysis confirmed a uniform coating layer formation of both formulations on urea granules. A slow release of N from ZnS and ZnSM was observed in water. After soil application, ZnSM decreased the NH3 emission by 38% compared to uncoated urea. Most of the soil parameters did not differ between ZnS and uncoated urea treatment. Microbial biomass N and Zn in ZnSM were 125 and 107% higher than uncoated urea, respectively. Soil mineral N in ZnSM was 21% higher than uncoated urea. Such controlled nutrient availability in the soil resulted in higher sunflower grain yield (53%), N (80%) and Zn (126%) uptakes from ZnSM than uncoated fertilizer. Hence, coating biopolymer with Zn on urea did not only increase the sunflower yield and N utilization efficiency but also meet the micronutrient Zn demand of sunflower. Therefore, coating urea with Zn plus biopolymer is recommended to fertilizer production companies for improving NUE, crop yield and reducing urea N losses to the environment in addition to fulfil crop micronutrient demand.

Low nitrogen (N) use efficiency from urea fertilizers due to environmental losses results in high cost of fertilizers for agricultural productions. Coating of urea with biodegradable polymers makes them effective for control and efficient N release. In this study, starch and polyvinyl alcohol (PVA) were used in combination with acrylic acid (AA), citric acid (CA) and maleic acid (MA) for the coating of urea prills. Different formulations of the coating were prepared and applied on urea prills such as urea coated with starch (10%) and PVA (5%) with acrylic acid: 2, 4 and 6% (USP-A2, USP-A4, USP-A6), with citric acid: 2, 4 and 6% (USP-C2, USP-C4, USP-C6), and with maleic acid: 2, 4 and 6% (USP-M2, USP-M4, USP-M6). After urea coating in fluidized bed coater, all uncoated and coated urea samples were characterized by scanning electron spectroscopy (SEM), Fourier transform infrared spectroscopy (FTIR), X-ray diffraction (XRD), crushing strength and UV-Vis spectroscopy. The morphological and XRD analysis indicated that a new uniform coating with no new phase transformation occurred. Among all urea coated samples, USP-A2 and USP-C2 showed the highest crushing strengths: 12.08 and 13.67 N with nitrogen release efficiency of 70.10 and 50.74% respectively. All coated urea samples improved the spinach plants’ foliage yield, chlorophyll content, N-uptake and apparent nitrogen recovery (ANR) than uncoated urea and control plants. However, USP-A2 and USP-C2 provided promising results among all coated samples with dry foliage yield (2208 ± 92 and 2428 ± 83 kg/ha), chlorophyll (34 ± 0.6 and 34 ± 0.4 mg/g), N-uptake (88 ± 4 and 95 ± 6 kg/ha) and ANR (59 ± 4 and 67 ± 6%). Therefore, urea prills coated with a combination of biodegradable polymers can be a better choice for the farmers to enhance agronomical productions by controlling the fertilizer nutrient release rate.

The low nitrogen utilization efficiency (NUE) of commercial fertilizers is one of the main hurdles in higher crop production and reduction of fertilizer N losses to the environment. However, interactions between most the macronutrients could have synergistic outcomes that affect crop NUE. The coating of urea with macronutrients and biopolymers may control N release and synergistically impact its crop NUE. In this study, urea was coated with 3% of different polymers, combined with 5% potassium iodide (KI) (i) Gum Arabica (GA + KI), (ii) polyvinyl alcohol (PVA + KI), and (iii) gelatin (Gelatin + KI) to control its N release, leaching, and increase of wheat NUE. Scanning electron microscopy, Fourier Transform Infrared spectroscopy (FTIR), and X-ray diffraction (XRD) analyses confirmed the successful coating of all KI and biopolymer combinations on urea granules. All coating combinations slowed down urea release in water and reduced its leaching from the soil, but the highest reduction in both parameters was observed with the GA + KI treatment, compared to the uncoated urea. After soil application, GA + KI decreased urea leaching by 26% than the uncoated urea in lysimeter. In the field, soil mineral N remained significantly high with the GA + KI and PVA + KI treatments at the wheat tillering, booting, grain filling and maturity stages, compared to the uncoated urea. However, K content was only high (28%) with the GA + KI treatment at final harvest. Likewise, microbial biomass N was only high with GA + KI at grain filling (20%) and maturity stages (24%) than the uncoated urea. Such synchronized N availability led to high wheat grain yield (28%), N (56%) uptake, and apparent N recovery (130%) with the GA + KI treatment, compared to the uncoated fertilizer. The increment in NUE with GA + KI could be due to the synergistic effect of K on N availability, therefore, we observed higher wheat yield and N utilization efficiency with this treatment. Hence, urea coated with macronutrient (K) plus biopolymer is recommended to improve wheat yield, NUE, and for reduction of environmental N losses.

The design of actively efficient and low-toxicity formulations against virulent bacterial strains causing skin infections remains a challenging task. The aim of the present study was to develop and evaluate in vitro a hydrogel impregnated with a known plant extract for topical applications against major skin bacteria. A poly(vinyl alcohol) (PVA)/gelatin hydrogel, namely HG, was prepared by esterification following the solution casting method. The gelling process was realized by cross-linking the synthetic polymer PVA and the biopolymer gelatin in the presence of hydrochloric acid (HCl). A crude extract of Nigella sativa seeds was then encapsulated in HG, and the resulting HGE was characterized morphologically (by Scanning Electron Microscopy (SEM)), structurally (by X-ray powder diffraction (XRD) and Fourier Transform Infrared (FTIR) spectroscopy), behaviorally (by swelling behavior), and biologically (by the agar well diffusion method). The results of HGE were compared to HG and HG impregnated with 10% acetic acid (HGAA). SEM sections of HGE revealed a dense and porous surface, suggesting a good hydrophilicity. X-ray diffractograms indicated that HGE and HG had a similar degree of crystallinity. FTIR spectra confirmed that esterification occurred between PVA and gelatin suggesting that the amine group is involved in the intercalation of the plant extract components in HG. Further, HGE was found to be as wettable and swellable as HG, suggesting a good biocompatibility. Eventually, HGE exerted a pronounced inhibitory effect against two major skin pathogens, the Gram-negative Pseudomonas aeruginosa and the Gram-positive Staphylococcus aureus, suggesting a good extract release. Taken together, the experimental data indicated that HGE might be a promising wound dressing.

Microfiltration flat sheet membranes of polyether sulfone (PES) were fabricated by incorporating varying concentrations of polymer and investigated the influence of substituting solvents. The membranes were prepared via immersion precipitation method. Different solvents that included NMP (N-methyl-2-pyrrolidone), DMF (dimethylformamide), and THF (tetrahydrofuran) were used to analyse their effect on the performance and morphology of the prepared membranes. Two different coagulation bath temperatures were used to investigate the kinetics of membrane formation and subsequent effect on membrane performance. The maximum water flux of 141 ml/cm2.h was observed using 21% of PES concentration in NMP + THF cosolvent system. The highest tensile strength of 29.15 MPa was observed using membrane prepared with 21% PES concentration in NMP as solvent and coagulation bath temperature of 25°C. The highest hydraulic membrane resistance was reported for membrane prepared with 21% PES concentration in NMP as solvent. Moreover, the lowest contact angle of 67° was observed for membrane prepared with 15% of PES concentration in NMP as solvent with coagulation bath temperature of 28°C. Furthermore, the Hansen solubility parameter was used to study the effect on the thermodynamics of membrane formation and found to be in good correlation with experimental observation and approach in the present work.

Mixed matrix membranes (MMMs) are synthesized for efficient CO

The rise in energy requirements and its shortfall in developing countries have affected socioeconomic life. Communities in remote mountainous regions in Asia are among the most affected by energy deprivation. This study presents the feasibility of an alternate strategy of supplying clean energy to the areas consisting of pristine mountains and forest terrain. Southeast Asia has a much-diversified landscape and varied natural resources, including abundant water resources. The current study is motivated by this abundant supply of streams which provides an excellent environment for run-of-river micro vertical axis water turbines. However, to limit the scope of the study, the rivers and streams flowing in northern areas of Pakistan are taken as the reference. The study proposes a comprehensive answer for supplying low-cost sustainable energy solutions for such remote communities. The suggested solution consists of a preliminary hydrodynamic design using Qblade, further analysis using numerical simulations, and finally, experimental testing in a real-world environment. The results of this study show that the use of microturbines is a very feasible option considering that the power generation density of the microturbine comes out to be approximately 2100 kWh/year/m2, with minimal adverse effects on the environment.

To improve the efficacy of existing classes of antibiotics (ciprofloxacin), allow dose reduction, and minimize related toxicity, this study was executed becausenew target-oriented livestock antimicrobials are greatly needed to battle infections caused by multidrug-resistant (MDR) strains. The present study aims to green synthesize a biocompatible nanohybrid of ciprofloxacin (CIP)-Ag/TiO2/chitosan (CS). Silver and titanium nanoparticles were green synthesized using Moringa concanensis leaves extract. The incorporation of silver (Ag) nanoparticles onto the surface of titanium oxidenanoparticles (TiO2NPs) was done by the wet chemical impregnation method, while the encapsulation of chitosan (CS) around Ag/TiO2 conjugated with ciprofloxacin (CIP) was done by the ionic gelation method. The synthesized nanohybrid (CIP-Ag/TiO2/CS) was characterized using standard techniques. The antibacterial potential, killing kinetics, cytotoxicity, drug release profile, andminimum inhibitory concentration (MIC) were determined. Field emission scanning electron microscopy (FESEM) and transmission electron microscopy (TEM) revealed spherical agglomerated nanoparticles (NPs) of Ag/TiO2 with particle sizes of 47–75 nm, and those of the CIP-Ag/TiO2/CS nanohybrid were in range of 20–80 nm. X-ray diffractometer(XRD)patterns of the hetero system transmitted diffraction peaks of anatase phase of TiO2 and centered cubic metallic Ag crystals. Fourier Transform Infrared spectroscopy (FTIR) confirmed the Ti-O-Ag linkage in the nanohybrid. The zeta potential of CIP-Ag/TiO2/CS nanohybrid was found (67.45 ± 1.8 mV), suggesting stable nanodispersion. The MIC of CIP-Ag/TiO2/CS was 0.0512 μg/mL, which is much lower than the reference value recorded by the global CLSI system (Clinical Laboratory Standards Institute). The CIP-Ag/TiO2/CS nanohybrid was found to be effective against mastitis causing MDR E. coli, killing kinetics showed an excellent reduction of E. coli cells at 6 h of treatment. Flow cytometry further confirmed antibacterial potential by computing 67.87% late apoptosis feature at 6 h of treatment, antibiotic release kinetic revealed a sustained release of CIP. FESEM and TEM confirmed the structural damages in MDR E. coli (multidrug-resistant Escherichia coli). The CIP-Ag/TiO2/CS nanohybrid was found to be biocompatible, as more than 93.08% of bovine mammary gland epithelial cells remained viable. The results provide the biological backing for the development of nanohybrid antibiotics at a lower MIC value to treat infectious diseases of cattle and improve the efficacy of existing classes of antibiotics by conjugation with nanoparticles.

Sadia Abid,1 Bushra Uzair,1 Muhammad Bilal Khan Niazi,2 Fehmida Fasim,3 Syeda Asma Bano,4 Nazia Jamil,5 Rida Batool,5 Shamaila Sajjad6 1Department of Biological Sciences, International Islamic University, Islamabad, Pakistan; 2School of Chemical & Materials Engineering, National University of Sciences and Technology, Islamabad, Pakistan; 3Discipline of Biomedical Science, Sydney Medical School, The University of Sydney, Sydney, NSW, Australia; 4Department of Microbiology, University of Haripur, Haripur, Pakistan; 5Department of Microbiology & Molecular Genetics, Punjab University, Lahore, Pakistan; 6Department of Physics, International Islamic University, Islamabad, PakistanCorrespondence: Bushra UzairDepartment of Biological Sciences, International Islamic University, New Campus, Female Block, Room No. 007, Islamabad, H-10, PakistanTel +92 33 1538 3988Fax +92 901 9815Email bushra.uzair@iiu.edu.pkIntroduction: Candida albicans is a major opportunistic pathogen that causes a wide range of human infections. Currently available therapeutic agents are limited for treating these fungal infections due to multidrug resistance as well as their nonbiodegradability, poor biocompatibility and toxicity. In order to battle these limitations, we have synthesized a polymeric system as microcarriers to deliver the antifungal drug. The objective of the present study was to immobilize MgO/CuO nanocomposite and nystatin-loaded MgO/CuO nanocomposites in nontoxic, nonimmunogenic, biodegradable and biocompatible sodium alginate microspheres for the first time.Materials and Methods: Nanoparticle-loaded sodium alginate microspheres were prepared by ionotropic gelation technique using calcium chloride as a cross-linker. Synthesized microspheres were characterized using standard characterization techniques and were evaluated for biological activity against MDR strain of C. albicans.Results: Characterization of microspheres by Fourier-transform infrared spectroscopy confirmed loading of Nys-MgO/CuO NPs, scanning electron microscopy (SEM) revealed rough spherical beads with a highly porous surface having an average size in the range of 8– 10 μm. X-ray diffraction (XRD) analyzed its semicrystalline structure. Entrapment efficiency of Nys-MgO/CuO NPs was 80% and release kinetic study revealed sustained and prolonged release of drug in pH 5.5. Flow cytometry analysis showed yeast cell death caused by Nys-MgO/CuO MS exhibits late apoptotic features. In cytotoxicity assay 5– 14 mg of microspheres did not cause hemolysis. Microspheres reduced virulence traits of C. albicans such as germ tube and biofilm formation were compromised at concentration of 5 mg/mL. Antimicrobial assessment results revealed a pronounced inhibitory effect against C. albicans.Conclusion: The in vitro experiments have shown promising results based on good stability, Nys-MgO/CuO NP-encapsulated microspheres can be used as a prolonged controlled release system against MDR pathogenic C. albicans.Keywords: microspheres, antimicrobial activity, nystatin, Candida, metal oxides

Methicillin-resistant Staphylococcus aureus (MRSA)-induced mastitis is one of the biggest animal welfare issues and economic burdens worldwide. As a possible effective treatment, ciprofloxacin (CIP)-loaded cerium oxide (CeO2)/chitosan (CS) nanocomposite was synthesized using an eco-friendly approach, characterized, and evaluated. From 350 mastitis-positive milk samples, 35 mecA-positive MRSA strains were confirmed by antibiotic sensitivity testing and PCR. CeO2 nanoparticles (NPs) were synthetized using the seeds' extract of Amomum subulatum (aka black cardamom/BC) as a reducing and capping agent, which was conjugated with CS by ionic gelation before CIP was nanoencapsulated. The resulting NPs were characterized physically (by using FESEM, TEM, EDS, XRD, FTIR, ZP, and UV-Vis spectrophotometry), biologically and pharmacologically (through in-vitro/ex-vivo antibacterial, cytotoxic, and drug release behavior assays). The CIP-nanocomposite was represented by pure, stable, small, pseudospherical NPs of crystalline nature. FTIR confirmed the surface linkage of CS and CIP in CeO2 NPs. CIP-CeO2/CS nanocarrier exerted enhanced antibacterial activity at lower MIC (8 μg/mL) compared to that of free CIP drug alone. Also, they were hemocompatible and not hepatotoxic. CIP release from the nanocarrier was better sustained in physiological-like conditions. Taken together, the phytogenic CIP-CeO2/CS nanocarrier could be considered as a potent and safe therapeutic solution for MRSA-induced mastitis.

Membranes with zeolites are encouraging for performing blood dialysis because zeolites can eliminate uremic toxins through molecular sieving. Although the addition of various pore-gen and adsorbent in the membrane can certainly impact the membrane production along with creatinine adsorption, however, it is not directed which pore-gen along with zeolite leads to better performance. The research was aimed at reducing the adsorption of protein-bound and uremic toxins by using mordenite zeolite as an adsorbent while polyethylene glycol and cellulose acetate as a pore generating agent. Membranes were cast by a phase-inversion technique which is cheap and easy to handle as compared to the electro-spinning technique. Through this strategy, the ability to adsorb creatinine and solute rejection percentage were measured and compared against the pristine PSU, when only PEG was used as a pore-modifier and when PEG along with CA was used as a pore-modifier along with a different concentration of zeolite. The experiments revealed that PEG membranes can give a better solute rejection percentage (93%) but with a low creatinine adsorption capacity that is 7654 μg/g and low bio-compatibility (PRT 392 s, HR 0.46%). However, PEG/CA membranes give maximum creatinine adsorption that is 9643 μg/g and also better bio-compatibility (PRT 490 s, HR 0.37%) but with a low BSA rejection (72%) as compared to the pristine PSU and PEG membranes. The present study finds that the concentration of mordenite zeolite affects the membrane performance because its entrapment and large pore size of the membrane decreases solute rejection but increases creatinine uptake level along with the better bio-compatibility.

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.

Low nitrogen (N) utilization efficiency due to environmental N losses from fertilizers results in high-cost on-farm production. Urea coating with biodegradable polymers can prevent these losses by controlling the N release of fertilizers. We calculated N release kinetics of coated granular with various biodegradable polymeric materials and its impact on spinach yield and N uptake. Different formulations were used, (i) G-1: 10% starch + 5% polyvinyl alcohol (PVA) + 5% molasses, (ii) G-2: 10% starch + 5% PVA + 5% paraffin wax (PW), (iii) G-3: 5% gelatin + 10% gum arabic + 5% PW, (iv) G-4: 5% molasses + 5% gelatin + 10% gum arabic, to coat urea using a fluidized bed coater. The morphological and X-ray diffraction (XRD) analyses indicated that a uniform coating layer with no new phase formation occurred. In the G-2 treatment, maximum crushing strength (72.9 N) was achieved with a slowed-down N release rate and increased efficiency of 31%. This resulted in increased spinach dry foliage yield (47%), N uptake (60%) and apparent N recovery (ANR: 130%) from G-2 compared to uncoated urea (G-0). Therefore, coating granular urea with biodegradable polymers is a good choice to slower down the N release rate and enhances the crop yield and N utilization efficiency from urea.

Because of the heavy reliance of people on limited fossil fuels as energy resources, global warming has increased to severe levels because of huge CO2 emission into the atmosphere. To mitigate this situation, a green method is presented here for the conversion of CO2/H2O into sustainable hydrocarbon fuels via electrolysis in eutectic molten salts [(KCl–LiCl; 41:59 mol %), (LiOH–NaOH; 27:73 mol %), (KOH–NaOH; 50:50 mol %), and (Li2CO3–Na2CO3–K2CO3; 43.5:31.5:25 mol %)] under the conditions of 1.5–2 V and 225–475 °C depending on the molten electrolyte used. Gas chromatography (GC) and GC–mass spectrometry (MS) techniques were employed to analyze the content of gaseous products. The electrolysis results in hydrocarbon production with maximum 59.30, 87.70, and 99% Faraday efficiencies in the case of molten chloride, molten hydroxide, and molten carbonate electrolytes under the temperatures of 375, 275, and 425 °C, respectively. GC with a flame-ionization detector and a thermal conductivity detector and GC–MS analysis confirmed that H2 and CH4 were the main products in the case of molten chlorides and hydroxides at an applied voltage of 2 V, while longer-chain hydrocarbons (>C1) were obtained only in molten carbonates at 1.5 V. In this way, electricity is transformed into chemical energy. The heating values obtained from the produced hydrocarbon fuels are satisfactory for further application. The practice of using molten salts could be a promising and encouraging technology for further fundamental investigation of sustainable hydrocarbon fuel formation with more product concentrations because of their fast electrolytic conversion rate without the use of a catalyst.

The application of urea-based fertilizers in developing countries has gained significant momentum over time. urea usage is to meet demand and supply gap of food resources as world population is increasing at a fast pace. urea contains largest content of nitrogen (46%) among all the solid nitrogenous fertilizers. However, main drawback of urea is its higher dissolution rate. After soil application, most of urea nitrogen is lost through a leaching, runoff, nitrification-denitrification and ammonia volatilization. To tackle urea related environmental pollution, development of slow-release urea fertilizer is a need of the hour and this would also increase product use efficiency in terms of crop productivity and its N uptake. We studied the usage of polymeric materials in combination with inorganic substances like sulfur and plaster of Paris as effective and biodegradable coating substances for urea prills. For coating on urea prills, fluidized bed coater was used whereas paraffin wax and molasses were used as binding agents. The urea was coated with four different formulations, i.e., C-1: PVA 5% + plaster of Paris 10% + sulfur 5% + paraffin wax 2%, C-2: PVA 5% + starch 10% + sulfur 5% + paraffin wax 2%, C-3: gelatin 5% + plaster of Paris 10% + sulfur 5% + paraffin wax 2% and C-4: PVA 5% + starch 10% + sulfur 5% + paraffin wax 2.5% + molasses 2.5%. Each formulation along with uncoated urea prills (C-0) were evaluated for characterization and N release kinetics. All the formulations along with uncoated urea were applied to spinach crop in pot experiment. A control (No N: untreated) was also kept. Spinach biomass yield and N uptake were determined. The formulation C-1 yielded highest urea-N release efficiency and spinach N uptake of6.87% and 1.93 g N/pot, respectively. Themodified Schwarz and Sinclair formula gave the excellent representation of release of nutrient-N from coated urea prills. It is concluded that coating urea prills with organic and inorganic blends is better option to slow down N release kinetics and improve spinach productivity. Therefore, by using coated fertilizers, farmers can improve agro-environmental value of urea, worldwide.

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.

Environmental concerns due to excessive use of synthetic or petroleum-based materials have encouraged scientists to develop novel, sustainable, and multifunctional material using abundant lignocellulosic biomass. In this work, a study was conducted on the isolation of cellulose from wheat straw using two different methods: acidified sodium chlorite and alkaline hydrogen peroxide. A comparative study was carried out based on the yield and properties of extracted cellulose. The final product (after treatments) was characterized by Fourier transform infrared spectroscopy (FT-IR), X-ray diffraction (XRD), and thermogravimetric analysis (TGA) for the identification of properties. Both the treatments isolated pure white color cellulose. However, the yield of cellulose isolated through acidified sodium chlorite treatment (81.4%) was higher than alkaline hydrogen peroxide treatment (79%). Moreover, no huge difference was observed in the crystallinity and thermal properties of extracted cellulose.

Biomaterials are in use for the replacement and reconstruction of several tissues and organs as treatment and enhancement. Metallic, organic, and composites are some of the common materials currently in practice. Metallic materials contribute a big share of their mechanical strength and resistance to corrosion properties, while organic polymeric materials stand high due to their biocompatibility, biodegradability, and natural availability. To enhance the biocompatibility of these metals and alloys, coatings are frequently applied. Organic polymeric materials and ceramics are extensively utilized for this purpose due to their outstanding characteristics of biocompatibility and biodegradability. Hydroxyapatite (HAp) is the material from the ceramic class which is an ultimate candidate for coating on these metals for biomedical applications. HAp possesses similar chemical and structural characteristics to normal human bone. Due to the bioactivity and biocompatibility of HAp, it is used for bone implants for regenerating bone tissues. This review covers an extensive study of the development of HAp coatings specifically for the orthopaedic applications that include different coating techniques and the process parameters of these coating techniques. Additionally, the future direction and challenges have been also discussed briefly in this review, including the coating of HAp in combination with other calcium magnesium phosphates that occur naturally in human bone.

Treatment of pandrug resistant (PDR) Escherichia coli strain is the leading causative agent of bovine mastitis worldwide. Hence, becoming a potential threat to veterinary and public health. Therefore, to control the infection new nontoxic, biocompatible antimicrobial formulation with enhanced antibacterial activity is massively required. Current study was planned to synthesize chitosan coated titanium dioxide nanoparticles (CS-NPs coated TiO2). Coating was being done by chitosan nanoparticles (CS-NPs) using ionic gelation method. Aqueous solution of Moringa concanensis leaf extract was used to synthesize titanium dioxide nanoparticles (TiO2 NPs). The synthesized nanoformulations were characterized by using XRD, SEM, and FTIR. X-ray diffraction (XRD) analysis indicated the crystalline phase of TiO2 NPs and CS-NPs coated TiO2 NPs. Scanning Electron Microscopy (SEM) confirmed spherical shaped nanoparticles size of chitosan NPs ranging from 19–25 nm and TiO2 NPs 35–50 nm. Thesize of CS-NPs coated TiO2 NPs was in the range of 65–75 nm. The UV-Vis Spectra and band gap values illustrated the red shift in CS-NPs coated TiO2 NPs. Fourier transform infrared (FTIR) spectroscopy confirmed the linkages between TiO2 NPs and chitosan biopolymer, Zeta potential confirmed the stability of CS-NPs coated TiO2 NPs by showing 95 mV peak value. In-vitro antibacterial activity of CS-NPs coated TiO2 NPs and Uncoated TiO2 NPs was evaluated by disc diffusion method against PDR strain of E. coli isolated from mastitic milk samples. The antibacterial activity of all the synthesized nanoformulations were noted and highest antibacterial activity was shown by CS-NPs coated TiO2-NPs against pandrug resistant (PDR) E. coli strain with the prominent zone of inhibition of 23 mm. Morphological changes of E. coli cells after the treatment with MIC concentration (0.78 μg/ml) of CS-NPs coated TiO2 NPs were studied by transmission electron microscopy TEM showedrigorous morphological defectand has distorted the general appearance of the E. coli cells. Cytotoxicity (HepG2 cell line) and hemolytic (human blood) studies confirmed nontoxic/biocompatible nature of CS-NPs coated biologically synthesized TiO2 NPs. The results suggested that biologically synthesized and surface modified TiO2 NPs by mucoadhesive polysaccharides (e.g. chitosan) coating would be an effective and non-toxic alternative therapeutic agent to be used in livestock industry to control drug resistant veterinary pathogens.

Deca-dodecasil 3 rhombohedral (DDR3) membrane has received much attention in CO2 separation from small gas molecules because of its molecular sieving property and stable characteristics. Therefore, the present work is focusing on the utilization of previously fabricated membrane (synthesized in 3 days as reported in our previous work) to study the effect of hydrocarbons and its durability at the previously optimized conditions. Subsequently, gas permeation study was conducted on the DDR3 membrane in CO2 separation from small gas molecules and it was found that the permeance of H2, CO2, N2, and CH4 decreased in the order of H2 > CO2 > N2 > CH4, according to the increase in kinetic diameter of these gas molecules. Besides, it was observed that the ideal selectivities of the gas pairs decreased in the sequence of CO2/CH4 > CO2/N2 > H2/CO2. On the other hand, it was found that the presence of hydrocarbon impurities in the gas mixture containing CO2 and CH4 has directly affected the performance of DDR3 membrane and contributed to the losses of CO2 permeability, CH4 permeability, and CO2/CH4 selectivity of 39.1%, 14.8%, and 4.2%, respectively. Consequently, from the stability test, the performance of DDR3 membrane remained stable for 96 h, even after the separation testing using CO2 and CH4 gas mixture containing hydrocarbon impurities.

Hydrogel is the most emblematic soft material which possesses significantly tunable and programmable characteristics. Polymer hydrogels possess significant advantages including, biocompatible, simple, reliable and low cost. Therefore, research on the development of hydrogel for biomedical applications has been grown intensely. However, hydrogel development is challenging and required significant effort before the application at an industrial scale. Therefore, the current work focused on evaluating recent trends and issues with hydrogel development for biomedical applications. In addition, the hydrogel's development methodology, physicochemical properties, and biomedical applications are evaluated and benchmarked against the reported literature. Later, biomedical applications of the nano-cellulose-based hydrogel are considered and critically discussed. Based on a detailed review, it has been found that the surface energy, intermolecular interactions, and interactions of hydrogel adhesion forces are major challenges that contribute to the development of hydrogel. In addition, compared to other hydrogels, nanocellulose hydrogels demonstrated higher potential for drug delivery, 3D cell culture, diagnostics, tissue engineering, tissue therapies and gene therapies. Overall, nanocellulose hydrogel has the potential for commercialization for different biomedical applications.

The effect of the viscosity of the casting suspension on membrane morphology and thickness has been investigated for polyvinyl alcohol (PVA)/crystalline nanocellulose (CNC) nanocomposite membranes used for CO 2 /CH 4 separation. Different concentrations of CNC suspended in dissolved PVA affected the viscosities of resulting suspensions. A methodology was developed to make equal viscosity suspensions with variable CNC content. SEM micrographs show that by increasing the concentration of CNC in PVA, the thickness of the selective layer increased. However, equal thickness was achieved by water dilution for viscosity adjustment. The overall objective of this work was to find the real optimum concentration of CNC in PVA for CO 2 /CH 4 separation independent of the membrane thickness. Furthermore, the effect of the relative humidity (RH) and feed pressure on the selectivity and permeability of the membranes were also investigated as part of this study. For 1.5% CNC in PVA with pH 9 in the casting suspension, tested at feed pressure of 5 bar, CO 2 /CH 4 selectivity was up to 39 and the achieved permeance was 0.27 m 3 (STP)/(m 2 h bar). Above this concentration of CNC, the CO 2 permeation and selectivity decreased. It was also observed that increasing pressure caused a decrease in the performance of the membranes for CO 2 capture in terms of both permeation and selectivity. Moreover, increasing RH causes increasing in CO 2 permeation and selectivity.