Urea-rich sodium alginate-based hydrogel fertilizer as a water reservoir and slow-release N carrier for tomato cultivation under different water-deficit levels.

In this study, a new eco-friendly urea-rich sodium alginate-based hydrogel with a slow-release nitrogen property was prepared, and its effectiveness was evaluated in the cultivation of tomato plants under different water stress levels. The structure and performance of the hydrogel were investigated by FTIR, XRD, TGA, DTG, and SEM. The swelling and release experiments showed that prepared urea-rich hydrogel exhibited a high-water holding capacity (412 ± 4 g/g) and showed a sustained and slow nitrogen release property. A greenhouse pot experiment was conducted using two hydrogel levels (0.1 and 0.5 wt%) under two water deficit levels (30 and 70 % based on required water irrigation). Germination tests indicated that the developed hydrogel fertilizer has no phytotoxicity and has a positive impact on the germination rate even under water deficit conditions. The application of hydrogel fertilizer at 0.5 wt% significantly (p > 0.05) enhanced plant growth parameters such as leaf number, chlorophyll content, stem diameter, and plant length compared to the control treatment. The magnitude of the responses to the hydrogel fertilizer application depended on the concentration of applied hydrogel fertilizer and stress severity with the most positive effects on the growth and yield of tomato observed at a level of 0.5 %. Tomato yield was significantly enhanced by 19.58 %-12.81 %, 18.58 %-22.02 %, and 39.38 %-43.18 % for the plant amended with hydrogel at 0.1-0.5 wt% and grown under water deficit levels of 0, 30, and 70 %, respectively, compared to the control treatment.

Nanocellulose: Structure, modification, biodegradation and applications in agriculture as slow/controlled release fertilizer, superabsorbent, and crop protection: A review.

This review investigates the potential of nanocellulose in agriculture, encompassing its structure, synthesis, modification, and applications. Our investigation of the characteristics of nanocellulose includes a comprehensive classification of its structure. Various mechanical, chemical and enzymatic synthesis techniques are evaluated, each offering distinct possibilities. The central role of surface functionalization is thoroughly examined. In particular, we are evaluating the conventional production of nanocellulose, thus contributing to the novelty. This review is a pioneering effort to comprehensively explore the use of nanocellulose in slow and controlled release fertilizers, revolutionizing nutrient management and improving crop productivity with reduced environmental impact. Additionally, our work uniquely integrates diverse applications of nanocellulose in agriculture, ranging from slow-release fertilizers, superabsorbent cellulose hydrogels for drought stress mitigation, and long-lasting crop protection via nanocellulose-based seed coatings. The study ends by identifying challenges and unexplored opportunities in the use of nanocellulose in agriculture. This review makes an innovative contribution by being the first comprehensive study to examine the multiple applications of nanocellulose in agriculture, including slow-release and controlled-release fertilizers.

Superabsorbent hydrogels based on natural polysaccharides: Classification, synthesis, physicochemical properties, and agronomic efficacy under abiotic stress conditions: A review.

Superabsorbent polymers (SAPs) are a class of polymers that have attracted tremendous interest due to their multifunctional properties and wide range of applications. The importance of this class of polymers is highlighted by the large number of publications, including articles and patents, dealing with the use of SAPs for various applications. Within this framework, this review provides an overview of SAPs and highlights various key aspects, such as their history, classification, and preparation methods, including those related to chemically or physically cross-linked networks, as well as key factors affecting their performance in terms of water absorption and storage. This review also examines the potential use of polysaccharides-based SAPs in agriculture as soil conditioners or slow-release fertilizers. The basic aspects of SAPs, and methods of chemical modification of polysaccharides are presented and guidelines for the preparation of hydrogels are given. The water retention and swelling mechanisms are discussed in light of some mathematical empirical models. The nutrient slow-release kinetics of nutrient-rich SAPs are also examined on the basic of commonly used mathematical models. Some examples illustrating the advantages of using SAPs in agriculture as soil conditioners and agrochemical carriers to improve crop growth and productivity are presented and discussed. This review also attempts to provide an overview of the role of SAPs in mitigating the adverse effects of various abiotic stresses, such as heavy metals, salinity, and drought, and outlines future trends and prospects.

Effect of sodium alginate-based superabsorbent hydrogel on tomato growth under different water deficit conditions.

The main challenge facing agriculture today is water scarcity. At present, agriculture consumes around 70 % of the planet's freshwater, much of which is lost through evaporation, leaching and runoff. This wastage, combined with the increased frequency and severity of droughts linked to climate change, is having a considerable negative impact on crops. As a result, the food security of people living in regions with limited water resources is threatened. In this regard, efficient water management using water-saving materials and soil additives such as superabsorbent polymers (SAPs) are recognized as an effective strategy to boost water use efficiency by plants and improve agricultural productivity. The present study fits with this strategy and aims to investigate the effect of new sodium alginate-based hydrogel-treated sandy loam soil on seed emergence and growth of tomatoes as a crop model under different water-deficit stress levels. A set of pot experiments was conducted in a greenhouse chamber using sandy loam soil amended with two levels of hydrogel (0.1 % and 0.5 % by weight) along with untreated control, all under water-deficit stress at three levels: 30 % of the daily amount of required irrigation water (DARW) for different growing cycles (severe stress), 70 % DARW (mild stress), and 100 % DARW (normal irrigation conditions). The germination test showed the absence of phytotoxicity of the developed hydrogel and confirmed its suitability in protecting seedlings from drought stress. Greenhouse experiment results demonstrated that water stress and levels of applied hydrogel significantly (P < 0.05) affected plant growth parameters such as plant height, stem diameter, number of leaves, chlorophyll content, fresh weight, and dry weight compared with the treatments without SAPs. The developed sodium alginate-based SAPs showed relevant agronomical benefits under drought stress by retaining more water and nutrients, thus it had the potential to be used in agriculture for better water management along with significant environmental benefits.

Ultrasound-assisted degradation of organophosphorus pesticide methidathion using CuFe2O4@SiO2-GOCOOH as a magnetic separable sonocatalyst.

Water contamination by pesticides is a critical environmental issue, necessitating the development of sustainable and efficient degradation methods. This study focuses on synthesizing and evaluating a novel heterogeneous sonocatalyst for degrading pesticide methidathion. The catalyst consists of graphene oxide (GO) decorated CuFe2O4@SiO2 nanocomposites. Comprehensive characterization using various techniques confirmed the superior sonocatalytic activity of the CuFe2O4@SiO2-GOCOOH nanocomposite compared to CuFe2O4@SiO2 alone. The enhanced performance is attributed to the combined effects of GO and CuFe2O4@SiO2, including increased surface area, enhanced adsorption capabilities, and efficient electron transfer pathways. Reaction parameters such as time, temperature, concentration, and pH significantly influenced the degradation efficiency of methidathion. Longer reaction times, higher temperatures, and lower initial pesticide concentrations favored faster degradation and higher efficiency. Optimal pH conditions were identified to ensure effective degradation. Remarkably, the catalyst demonstrated excellent recyclability, indicating its potential for practical implementation in pesticide-contaminated wastewater treatment. This research contributes to the development of sustainable methods for environmental remediation, highlighting the promising potential of the graphene oxide decorated CuFe2O4@SiO2 nanocomposite as an effective heterogeneous sonocatalyst for pesticide degradation.

Starch-based controlled release fertilizers: A review.

Starch, as a widely available renewable resource, has the potential to be used in the production of controlled-release fertilizers (CRFs) that support sustainable agriculture. These CRFs can be formed by incorporating nutrients through coating or absorption, or by chemically modifying the starch to enhance its ability to carry and interact with nutrients. This review examines the various methods of creating starch-based CRFs, including coating, chemical modification, and grafting with other polymers. In addition, the mechanisms of controlled release in starch-based CRFs are discussed. Overall, the potential benefits of using starch-based CRFs in terms of resource efficiency and environmental protection are highlighted.

Eco-friendly approach to access of quinoxaline derivatives using nanostructured pyrophosphate Na2PdP2O7 as a new, efficient and reusable heterogeneous catalyst.

In the present study, we report the synthesis of various quinoxaline derivatives from direct condensation of substituted aromatic 1,2-diamine with 1,2-dicarbonyl catalyzed by nanostructured pyrophosphate Na2PdP2O7 as a new highly efficient bifunctionalheterogeneous catalyst. The quinoxaline synthesis was performed in ethanol as a green and suitable solvent at ambient temperature to afford the desired quinoxalines with good to excellent yields in shorter reaction times. Many Quinoxaline derivatives were successfully synthesized using various 1,2-diketones and 1,2-diamines at room temperature. Catalyst reusability showed that the Na2PdP2O7 catalyst exhibited excellent recyclability without significant loss in its catalytic activity after five consecutive cycles.

Surface modification of highly hydrophobic polyester fabric coated with octadecylamine-functionalized graphene nanosheets.

This study focuses on the design of highly hydrophobic polyester fabrics (PET) coated with organophilic graphene nanosheets (G-ODA) through a simple, cost-effective and scalable coating method. The organophilic graphene oxide was successfully synthesized by covalently grafting a long chain fatty amine on its surface and was fully characterized by various physicochemical techniques. G-ODA was coated at different loadings onto the PET fabric ranging from 1 to 7 wt% to produce uniformly dispersed PET@G-ODA fabrics with multifunctional performances. FTIR has confirmed the formation of strong interfacial interaction between the PET and G-ODA functional groups. Moreover, the produced PET@G-ODA fabrics resulted in achieving enhanced thermal stability as well as excellent water repellency compared to the pristine PET. Water contact angle measurements showed a tremendous enhancement of surface hydrophobicity up to 148° with 7 wt% loading of G-ODA. Tensile strength tests revealed that our fabric exhibited excellent mechanical properties compared to neat PET. In addition, the designed PET@G-ODA fabrics demonstrated excellent oil/water separation efficiency for different oil/water mixtures. The obtained results are very promising in terms of designing and producing functional PET fabrics with improved thermal and surface proprieties.

Biodiesel production from rapeseed oil and low free fatty acid waste cooking oil using a cesium modified natural phosphate catalyst.

The present study focuses on the catalytic activity of cesium modified natural phosphate in biodiesel production from rapeseed oil and low free fatty acids (FFA) used in cooking oil. The catalyst was prepared by impregnation of cesium chloride (CsCl) on the natural phosphate followed by calcination up to 800 °C. The phosphate based catalyst was thermally, structurally, morphologically, and texturally characterized in order to determinate the relationship between its physicochemical properties and its catalytic activity. The chosen catalyst was demonstrated to be an active catalyst for the transesterification of rapeseed oil achieving a biodiesel yield of 99.55% under suitable reaction conditions: a methanol to oil molar ratio of 12 : 1, reaction temperature of 70 °C, catalyst amount of 4 wt% based on oil weight and reaction time of 6 h. Results from low FFA waste cooking oil transesterification indicated that a methyl esters yield of 99.52% could be obtained. Furthermore, results from esterification/transesterification of acidified rapeseed oil indicate that a yield of 93% may be obtained, thus giving rise to a potential application in 2nd generation biodiesel production from low acidic oils. Some important physicochemical properties of the obtained biodiesel were evaluated and compared with the EN14214 and ASTM D-6751 standards for biodiesel specifications.

Effective removal of Cu(II) from aqueous solution over graphene oxide encapsulated carboxymethylcellulose-alginate hydrogel microspheres: towards real wastewater treatment plants.

In the current study, the graphene oxide (GO) encapsulated carboxymethyl cellulose-Alginate (CMC-Alg) hydrogel microspheres were prepared via ionotropic gelation method and characterized using FTIR, TGA, SEM-EDS and surface charge by determining pHpzc. The adsorption of Cu2+ ions from aqueous solution on the graphene oxide embedded CMC-Alg was studied under different experimental conditions, and the results showed that embedded beads had high adsorption capacity compared with pure CMC-Alg beads due to synergetic effect between functional groups GO and CMC-Alg matrix. Adsorption capacities at equilibrium were calculated experimentally as 22.10, 39.96, 41.72 and 64 mg/g for pure CMC-Alg, CMC-Alg/GO 1%, CMC-Alg/GO 3% and CMC-Alg/GO 5%, respectively. The adsorption kinetics were found to follow the pseudo-second-order, and the equilibrium data fitted well with the Langmuir adsorption isotherm. Moreover, the intraparticle diffusion model has been inspected pointing that the adsorption process was found to be sequence of surface adsorption and intraparticle diffusion (IPD). The results suggest that graphene oxide embedded CMC-Alg bead matrix can be efficiently used as an adsorbent for metal ions removal from wastewater.

Aqueous-phase catalytic hydroxylation of phenol with H2O2 by using a copper incorporated apatite nanocatalyst.

Copper incorporated apatite (Cu-apatite) nanomaterial was prepared by a co-precipitation method. The obtained material was characterized by thermogravimetric analysis (TGA), X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), Fourier transform infrared (FT-IR) and Raman spectroscopy, scanning electron microscopy (SEM, STEM) and nitrogen adsorption-desorption. The as-prepared Cu-apatite was used to catalyze phenol hydroxylation with hydrogen peroxide as an oxidant. The influencing parameters including reaction time, temperature, H2O2/phenol ratio and catalyst mass have been investigated. Under the optimized conditions, the Cu-apatite catalyst gave a phenol conversion of 64% with 95% selectivity to dihydroxybenzenes. More importantly, the results of catalyst recycling indicated that the same catalytic performance has been obtained after four cycles with a slight loss of activity and selectivity.

Iron oxide encapsulated by copper-apatite: an efficient magnetic nanocatalyst for N-arylation of imidazole with boronic acid.

N-Arylation of imidazole was carried out with various arylboronic acids on iron oxide encapsulated by copper-apatite (Fe3O4@Cu-apatite), producing excellent yields. Firstly, the iron nanoparticles were prepared using a solvothermal method, and then they were encapsulated by copper-apatite to obtain magnetic Fe3O4@Cu-apatite nanocatalysts. Several physico-chemical analysis techniques were used to characterize the prepared nanostructured Fe3O4@Cu-apatite catalyst. The prepared Fe3O4@Cu-apatite was used as a nanocatalyst for N-arylation of imidazole with a series of arylboronic acids with different substituents to reaffirm the effectiveness of this magnetic nanocatalyst. The Fe3O4@Cu-apatite nanocatalyst can also be easily separated from the reaction mixture using an external magnet. More importantly, the as-prepared Fe3O4@Cu-apatite exhibited good reusability and stability properties in successive cycles. However, there was a notable loss of its catalytic activity after multiple cycles.

Response surface methodology for optimization of methylene blue adsorption onto carboxymethyl cellulose-based hydrogel beads: adsorption kinetics, isotherm, thermodynamics and reusability studies.

Environment-friendly composite hydrogel beads based on carboxymethyl cellulose (CMC), alginate (Alg) and graphene oxide (GO) were synthesized by an ionotropic gelation technique and studied as an efficient adsorbent for methylene blue (MB). The chemical structure and surface morphology of the prepared hydrogel beads were characterized by Fourier transform infrared spectroscopy (FTIR), scanning electron microscopy (SEM), thermogravimetric analysis (TGA), differential thermal analysis (DTA) and point of zero charge (pHpzc). A hybrid response surface methodology integrated Box-Behnken design (RSM-BBD) was successfully developed to model, simulate, and optimize the biosorption process. The synergistic effects between three critical independent variables including adsorbent dose (0.3-0.7 g), pH of the MB solution (6.5-9.5) and initial MB concentration (15-45 mg L-1) on the MB adsorption capacity (mg g-1) and removal efficiency (%) were statistically studied and optimized. The performance of the RSM-BBD method was found to be very impressive and efficient. Results proved that the adsorption process follows a polynomial quadratic model since high regression parameters were obtained (R 2-value = 99.8% and adjusted R 2-value = 99.3%). Analysis of variance (ANOVA) further confirms the validity of the suggested model. The optimal conditions for 96.22 ± 2.96% MB removal were predicted to be 0.6 g of CMC-Alg/GO hydrogel beads, MB concentration of 15 mg L-1 and pH of 9.5 within 120 min. The adsorption equilibrium is better described by the Freundlich isotherm, indicating that physisorption is the rate controlling mechanism. The MB adsorption process was thermodynamically spontaneous and endothermic. A reusability study revealed that the prepared adsorbent is readily reusable. The adsorbent still maintains its ability to adsorb MB for up to four cycles. Results reported in this study demonstrated that CMC-Alg/GO hydrogel beads are an effective, promising and recyclable adsorbent for the removal of MB from aqueous solutions.

Highly efficient catalytic/sonocatalytic reduction of 4-nitrophenol and antibacterial activity through a bifunctional Ag/ZnO nanohybrid material prepared via a sodium alginate method.

In this work, a bifunctional nanohybrid silver/zinc oxide material (Ag/ZnO) has been synthesized by a rapid route using sodium alginate simultaneously as a sacrificial template and silver reducing agent. The obtained samples were characterized by X-ray diffraction (XRD) and Fourier transform infrared (FTIR) spectroscopy, scanning electron microscopy (SEM), transmission electron microscopy (TEM), solid diffuse reflectance and liquid state UV-visible spectroscopy (DRS, UV-visible), and nitrogen adsorption-desorption analysis (BET-BJH). The XRD patterns showed that the Ag/ZnO sample is composed of a hexagonal zinc oxide structure with cubic metallic silver (Ag°). SEM micrographs exhibited a porous structure which was confirmed by BET-BJH methods to be mesoporous. The Ag/ZnO material was used as a nanocatalyst in the conversion of 4-nitrophenol (4-NP) to 4-aminophenol (4-AP) as well as an antibacterial agent against Escherichia coli and Staphylococcus aureus. It was found that an efficient 4-NP reduction to 4-AP in the presence of NaBH4 shows a rate constant of 0.418 min-1 under ultrasonic energy and 0.316 min-1 without ultrasonic energy. Both the catalysis reaction and antibacterial activity analysis were conducted in water solution and showed a synergetic effect of metallic silver loading.

Magnetic CoFe2O4 nanoparticles supported on graphene oxide (CoFe2O4/GO) with high catalytic activity for peroxymonosulfate activation and degradation of rhodamine B.

Herein, we report the preparation of magnetic CoFe2O4 nanoparticles and CoFe2O4/graphene oxide (GO) hybrids and evaluate their catalytic activity as heterogeneous peroxymonosulfate (PMS) activators for the decomposition of rhodamine B. The surface morphologies and structures of both CoFe2O4 nanoparticles and CoFe2O4/GO hybrids were investigated by powder X-ray diffraction (XRD), scanning electron microscopy (SEM), energy-dispersive X-ray spectroscopy (EDS), Fourier transform infrared spectroscopy (FTIR) and nitrogen adsorption-desorption isotherms. The magnetic properties of the samples were assessed using a SQUID magnetometer at 298 K. Catalytic oxidation experiments demonstrated that CoFe2O4/GO hybrids exhibited much better catalytic activity than CoFe2O4 nanoparticles or CoFe2O4/reduced graphene oxide (rGO) hybrids, suggesting that GO plays an important role in CoFe2O4/GO hybrids in the decomposition of rhodamine B. The influence of various reaction conditions such as temperature, concentration of PMS, pH and decomposition time of rhodamine B over the CoFe2O4/GO catalyst were investigated and optimized. The rhodamine B degradation process was found to fit a pseudo-first order kinetics model. The catalyst could be easily separated from the reaction mixture by applying an external magnet. In particular, the as-prepared CoFe2O4/GO hybrid exhibited good reusability and stability in successive degradation experiments in PMS solution.

Supercritical CO2 drying of alginate/zinc hydrogels: a green and facile route to prepare ZnO foam structures and ZnO nanoparticles.

In the present study, we investigate a simple and effective synthetic protocol to produce zinc oxide foams by a facile solution-based method using alginate gelation. The influences of the zinc concentration and the drying process on the structural, textural and morphological properties of the synthesized ZnO nanomaterial were studied and discussed. The components of these nanomaterials were characterized by several techniques to demonstrate the effectiveness of the adopted synthetic route in controlling the growth of the ZnO nanoparticles. XRD analysis revealed that the as-prepared ZnO nanomaterial crystallizes in the hexagonal wurtzite structure. The room temperature photoluminescence (PL) spectra of ZnO show ultra-violet (UV) and visible emissions. SEM analysis revealed the porous texture of the prepared zinc oxide. TEM analysis confirmed the nano dimensions of the synthesized zinc oxide nanoparticles. A comparative study of conventional air drying versus supercritical drying was conducted to determine the influence of each mode of drying on the structural, textural and morphological as well as optical properties of the synthesized ZnO nanoparticles.

Graphene Oxide Filled Lignin/Starch Polymer Bionanocomposite: Structural, Physical, and Mechanical Studies.

In this study, graphene oxide (GO) was investigated as a potential nanoreinforcing agent in starch/lignin (ST/L) biopolymer matrix. Bionanocomposite films based on ST/L blend matrix and GO were prepared by solution-casting technique of the corresponding film-forming solution. The structures, morphologies, and properties of bionanocomposite films were characterized by Fourier transform infrared (FTIR), thermal gravimetric analysis (TGA), ultraviolet-visible (UV-vis), SEM, and tensile tests. The experimental results showed that content of GO have a significant influence on the mechanical properties of the produced films. The results revealed that the interfacial interaction formed in the bionanocomposite films improved the compatibility between GO fillers and ST/L matrix. The addition of GO also reduced moisture uptake (Mu) and water vapor permeability of ST/L blend film. In addition, TGA showed that the thermal stability of bionanocomposite films was better than that of neat starch film. These findings confirmed the effectiveness of the proposed approach to produce biodegradable films with enhanced properties, which may be used in packaging applications.