Sustainable SMART fertilizers in agriculture systems: A review on fundamentals to in-field applications.

Agriculture will face the issue of ensuring food security for a growing global population without compromising environmental security as demand for the world's food systems increases in the next decades. To provide enough food and reduce the harmful effects of chemical fertilization and improper disposal or reusing of agricultural wastes on the environment, will be required to apply current technologies in agroecosystems. Combining biotechnology and nanotechnology has the potential to transform agricultural practices and offer answers to both immediate and long-term issues. This review study seeks to identify, categorize, and characterize the so-called smart fertilizers as the future frontier of sustainable agriculture. The conventional fertilizer and smart fertilizers in general are covered in the first section of this review. Another key barrier preventing the widespread use of smart fertilizers in agriculture is the high cost of materials. Nevertheless, smart fertilizers are widely represented on the world market and are actively used in farms that have already switched to sustainable technologies. The advantages and disadvantages of various raw materials used to create smart fertilizers, with a focus on inorganic and organic materials, synthetic and natural polymers, along with their physical and chemical preparation processes, are contrasted in the following sections. The rate and the mechanism of release are covered. The purpose of this study is to provide a deep understanding of the advancements in smart fertilizers during the last ten years. Trends are also recognized and studied to provide insight for upcoming agricultural research projects.

MXene-Based Nanocomposites for Piezoelectric and Triboelectric Energy Harvesting Applications.

Due to its superior advantages in terms of electronegativity, metallic conductivity, mechanical flexibility, customizable surface chemistry, etc., 2D MXenes for nanogenerators have demonstrated significant progress. In order to push scientific design strategies for the practical application of nanogenerators from the viewpoints of the basic aspect and recent advancements, this systematic review covers the most recent developments of MXenes for nanogenerators in its first section. In the second section, the importance of renewable energy and an introduction to nanogenerators, major classifications, and their working principles are discussed. At the end of this section, various materials used for energy harvesting and frequent combos of MXene with other active materials are described in detail together with the essential framework of nanogenerators. In the third, fourth, and fifth sections, the materials used for nanogenerators, MXene synthesis along with its properties, and MXene nanocomposites with polymeric materials are discussed in detail with the recent progress and challenges for their use in nanogenerator applications. In the sixth section, a thorough discussion of the design strategies and internal improvement mechanisms of MXenes and the composite materials for nanogenerators with 3D printing technologies are presented. Finally, we summarize the key points discussed throughout this review and discuss some thoughts on potential approaches for nanocomposite materials based on MXenes that could be used in nanogenerators for better performance.

ZnO/Graphene Composite from Solvent-Exfoliated Few-Layer Graphene Nanosheets for Photocatalytic Dye Degradation under Sunlight Irradiation.

ZnO/graphene nanocomposites were prepared using a facile approach. Graphene nanosheets were prepared by ultrasonication-based liquid phase exfoliation of graphite powder in a low boiling point organic solvent, 1,2-Dichloroethane, for the preparation of ZnO/graphene nanocomposites. Structural properties of the synthesized ZnO/graphene nanocomposites were studied through powder XRD and micro-Raman analysis. The characteristic Raman active modes of ZnO and graphene present in the micro-Raman spectra ensured the formation of ZnO/graphene nanocomposite and it is inferred that the graphene sheets in the composites were few layers in nature. Increasing the concentration of graphene influenced the surface morphology of the ZnO nanoparticles and a flower shape ZnO was formed on the graphene nanosheets of the composite with high graphene concentration. The efficiencies of the samples for the photocatalytic degradation of Methylene Blue dye under sunlight irradiation were investigated and 97% degradation efficiency was observed. The stability of the nanocomposites was evaluated by performing five cycles, and 92% degradation efficiency was maintained. The observed results were compared with that of ZnO/graphene composite derived from other methods.

MXene/Ferrite Magnetic Nanocomposites for Electrochemical Supercapacitor Applications.

MXene has been identified as a new emerging material for various applications including energy storage, electronics, and bio-related due to its wider physicochemical characteristics. Further the formation of hybrid composites of MXene with other materials makes them interesting to utilize in multifunctional applications. The selection of magnetic nanomaterials for the formation of nanocomposite with MXene would be interesting for the utilization of magnetic characteristics along with MXene. However, the selection of the magnetic nanomaterials is important, as the magnetic characteristics of the ferrites vary with the stoichiometric composition of metal ions, particle shape and size. The selection of the electrolyte is also important for electrochemical energy storage applications, as the electrolyte could influence the electrochemical performance. Further, the external magnetic field also could influence the electrochemical performance. This review briefly discusses the synthesis method of MXene, and ferrite magnetic nanoparticles and their composite formation. We also discussed the recent progress made on the MXene/ferrite nanocomposite for potential applications in electrochemical supercapacitor applications. The possibility of magnetic field-assisted supercapacitor applications with electrolyte and electrode materials are discussed.

Use of activated carbon and camphor carbon as cathode and clay cup as proton exchange membrane in a microbial fuel cell for the bioenergy production from crude glycerol biodegradation.

This work characterizes two alternative materials to substitute the most expensive microbial fuel cells (MFCs) components: proton exchange membrane (PEM) and cathode. Crude glycerol biodegradation was studied in MFCs using a clay cup as a PEM and activated carbon and camphor carbon mixture (CAC) as a cathode. The cathode performance was compared with Platinum on carbon cloth. Two clay cup single-chamber MFCs were operated with each cathode and fed with 2000 mg/L of crude glycerol. Electrochemical properties were characterized by linear sweep voltammetry, electrochemical impedance spectroscopy, and chronoamperometry. Biodegradation efficiencies were estimated with the chemical oxygen demand (COD) removal percentage. MFCs with CAC showed a maximum power density of 100 mW/m2. This result was a 43.47% power response regarding MFCs with Platinum. COD removal efficiencies of 94% were achieved in 37 days for both cells. The Columbic efficiencies were 24.04% and 22.78% for the MFCs with Platinum and CAC. The economic analysis showed a cost of USD 9.97 for MFCs with CAC. This cost is five times lower than when using Platinum. MFCs utilizing clay cups and CAC showed an acceptable performance for the bioenergy production from crude glycerol biodegradation above all economic advantage in the cell cost.

Improvement of zero waste sustainable recovery using microbial energy generation systems: A comprehensive review.

Microbial energy generation systems, i.e., bioelectrochemical systems (BESs) are promising sustainable technologies that have been used in different fields of application such as biofuel production, biosensor, nutrient recovery, wastewater treatment, and heavy metals removal. However, BESs face great challenges such as large-scale application in real time, low power performance, and suitable materials for their configuration. This review paper aimed to discuss the use of BES systems such as conventional microbial fuel cells (MFCs), as well as plant microbial fuel cell (P-MFC), sediment microbial fuel cell (S-MFC), constructed wetland microbial fuel cell (CW-MFC), osmotic microbial fuel cell (OsMFC), photo-bioelectrochemical fuel cell (PBFC), and MFC-Fenton systems in the zero waste sustainable recovery process. Firstly, the configuration and electrode materials used in BESs as the main sources to improve the performance of these technologies are discussed. Additionally, zero waste recovery process from solid and wastewater feedstock, i.e., energy recovery: electricity generation (from 12 to 26,680 mW m-2) and fuel generation, i.e., H2 (170 ± 2.7 L-1 L-1 d-1) and CH4 (107.6 ± 3.2 mL-1 g-1), nutrient recovery of 100% (PO43-P), and 13-99% (NH4+-N), heavy metal removal/recovery: water recovery, nitrate (100%), sulfate (53-99%), and sulfide recovery/removal (99%), antibiotic, dye removal, and other product recovery are critically analyzed in this review paper. Finally, the perspective and challenges, and future outlook are highlighted. There is no doubt that BES technologies are an economical option for the simultaneous zero waste elimination and energy recovery. However, more research is required to carry out the large-scale application of BES, as well as their commercialization.

Insight into BDD electrochemical oxidation of florfenicol in water: Kinetics, reaction mechanism, and toxicity.

Antibiotics in the environment provoke serious consequences on living beings and can be effectively remediated by prominent advanced oxidation process. In this study, electrochemical advanced oxidation treatment in a lab-scale reactor for the degradation of florfenicol (FLO) was studied with the aid of boron-doped diamond anode (BDD). The results exhibited that the FLO degradation follows pseudo-first-order kinetics. As the current intensity rose from 60 mA to 250 mA, the FLO removal efficiency increased and the corresponding reaction rate constant increased from 0.0213 to 0.0343 min-1, which was likely due to the more efficient participation of free hydroxyl radical (•OH) generated at the BDD anode. Faster degradation and higher mineralization of electrolyzed FLO solution were achieved at higher current intensity as well as in higher SO42- concentration medium, as a consequence of catalytic participation of oxidants (free •OH as well as sulfate radical (SO4•-) and persulfate (S2O82-)). The increase in FLO concentration from 30 to 50 mg L-1 resulted in a reaction rate constant decrease (from 0.0235 to 0.0178 min-1). Eight transformation by-products (m/z = 372.99, 359.8, 338.0, 324.04, 199.00, 185.02, 168.99 and 78.989) and three inorganic ions (NO3-, Cl- and F-) were analyzed by UPLC‒Q‒TOF‒MS/MS and Ion‒chromatography, respectively. The Vibrio fischeri bioluminescence inhibition revealed an increase of toxicity during the electrochemical oxidation that could be attributed mostly to the generated organic chlorinated by-products (m/z = 372.99, 359.8) and inorganic species (ClO2- and ClO3-).

Electricity generation from Nopal biogas effluent using a surface modified clay cup (cantarito) microbial fuel cell.

A modified clay cup (cantarito) microbial fuel cell (C-MFCs) was designed to digest the biomass effluent from a nopal biogas (NBE). To improve the process, commercial acrylic varnish (AV) was applied to the C-MFCs. The experiment was performed as:Both-C-MFCs, painting of AV on both sides of the clay cup; In-C-MFCs, painting of AV on the internal side, and Out-C-MFCs painting of AV on the external side. The order for the maximum volumetric power densities were Both-C-MFCs (1841.99 mW/m3)>Out-C-MFCs (1023.74 mW/m3) >In-C-MFCs (448.90 mW/m3). The control experiment without applied varnish did not show a stable potential, supporting the idea that the acryloyl group in varnish could favor the performance. Finally, a 4-digits clock was powered with two, Both-C-MFCs connected in series; the microbial diversity in this format was explored and a well-defined bacterial community including members of the phyla Actinobacteria, Bacteroidetes, Firmicutes, Proteobacteria, Synergistetes and candidate division TM7 was found.

Synthesis, antibacterial studies, and molecular modeling studies of 3,4-dihydropyrimidinone compounds.

The syntheses of dihydropyrimidinones (DHPMs) using solvent-free grindstone chemistry method. All the synthesized compounds exhibited significant activity against pathogenic bacteria. The current effort has been developed to obtain new DHPM derivatives that focus on the bacterial ribosomal A site RNA as a drug target. Molecular docking simulation analysis was applied to confirm the target specificity of DHPMs. The crystal structure of bacterial 16S rRNA and human 40S rRNA was taken as receptors for docking. Finally, the docking score, binding site interaction analysis revealed that DHPMs exhibit more specificity towards 16S rRNA than known antibiotic amikacin. Accordingly, targeting the bacterial ribosomal A site RNA with potential drug leads promises to overcome the bacterial drug resistance. Even though, anti-neoplastic activities of DHPMs were also predicted through prediction of activity spectra for substances (PASS) tool. Further, the results establish that the DHPMs can serve as perfect leads against bacterial drug resistance.