Magnetite nanoparticles decorated on cellulose aerogel for p-nitrophenol Fenton degradation: Effects of the active phase loading, cross-linker agent and preparation method.

Magnetite nanoparticles (Fe3O4 NPs) are among the most effective Fenton-Like heterogeneous catalysts for degrading environmental contaminants. However, Fe3O4 NPs aggregate easily and have poor dispersion stability because of their magnetic properties, which seriously decrease their catalytic efficiency. In this study, a novel environmentally friendly method for synthesising Fe3O4@CA was proposed. Fe3O4 NPs were immobilized on the 3D cellulose aerogels (CAs) in order to augment the degradation efficiency of p-nitrophenol (PNP) treatment and make the separation of the catalyst accessible by vacuum filtration method. Besides, CAs were fabricated from a cellulose source extracted from water hyacinth by using different cross-linking agents, such as kymene (KM) and polyvinyl alcohol-glutaraldehyde system (PVA-GA), and other drying methods, including vacuum thermal drying and freeze drying, were evaluated in the synthesis process. As-synthesized samples were analysed by various methods, including Powder X-ray diffraction, Fourier transform infrared spectroscopy, field emission scanning electron microscopy, energy dispersive X-ray analysis and Brunauer-Emmett-Teller. Then, using ultraviolet-visible spectroscopy, the difference in the degradability of PNP of the obtained material samples was also investigated to determine their potential applications. Results highlighted that the Fe3O4-3@CA-KF catalyst with an Fe3O4 loading of 0.40 g/gCA used KM as a cross-linker and the freeze-drying method demonstrated the highest PNP removal efficiency (92.5 %) in all Fe3O4@CA samples with a H2O2 content of 5 g/L. The degradation kinetics and well-fitted pseudo-first-order model were investigated. Notably, after five successive PNP degradation experiments, this catalyst retained ∼80 % of the ability to degrade PNP, indicating its outstanding reusability. In environmental remediation, this study provides valuable insights into the development of simply separated and high-efficiency catalysts for heterogeneous catalytic reactions.

Durian Shell-Mediated Simple Green Synthesis of Nanocopper against Plant Pathogenic Fungi.

The synthesis of fungicides in eco-friendly and cost-effective ways is significantly essential for agriculture. Plant pathogenic fungi cause many ecological and economic issues worldwide, which must be treated with effective fungicides. Here, this study proposes the biosynthesis of fungicides, which combines copper and Cu2O nanoparticles (Cu/Cu2O) synthesized using durian shell (DS) extract as a reducing agent in aqueous media. Sugar and polyphenol compounds contained in DS, as the main phytochemicals acting in the reduction procedure, were extracted under different temperatures and duration conditions to obtain the highest yields. We confirmed the extraction process performed at 70 °C for 60 min to be the most effective in extracting sugar (6.1 g/L) and polyphenols (22.7 mg/L). We determined the suitable conditions for Cu/Cu2O synthesis using a DS extract as a reducing agent for a synthesis time of 90 min, a volume ratio of DR extract/Cu2+ of 15:35, an initial pH solution of 10, a synthesis temperature of 70 °C, and a CuSO4 concentration of 10 mM. The characterization results of as-prepared Cu/Cu2O NP showed a highly crystalline structure of Cu2O and Cu with sizes estimated in the range of 40-25 nm and 25-30 nm, respectively. Through in vitro experiments, the antifungal efficacy of Cu/Cu2O against Corynespora cassiicola and Neoscytalidium dimidiatum was investigated by the inhibition zone. The green-synthesized Cu/Cu2O nanocomposites, which are potential antifungals against plant pathogens, exhibited excellent antifungal efficacy against both Corynespora cassiicola (MIC = 0.25 g/L, the diameter of the inhibition zone was 22.00 ± 0.52 mm) and Neoscytalidium dimidiatum (MIC = 0.0625 g/L, the diameter of the inhibition zone was 18.00 ± 0.58 mm). Cu/Cu2O nanocomosites prepared in this study could be a valuable suggestion for the control of plant pathogenic fungi affecting crop species globally.

Green Orange Peel-Mediated Bioinspired Synthesis of Nanoselenium and Its Antibacterial Activity against Methicillin-Resistant Staphylococcus aureus.

In this study, green orange peel (GOP) was feasibly evidenced in preparing selenium nanoparticles (SeNPs). Acting as reducing agents, polyphenolic compounds were extracted from GOP at the optimal extraction conditions (at 70 °C for 1.5 h, mass ratio of dried orange peel/distilled water of 5/100). The formation of SeNPs was observed at the wavelength range of 250-300 nm by ultraviolet-visible spectroscopy (UV-vis), and their highest yield could be reached at the following conditions: volume ratio of extract/selenious acid solution (V Ext/V Se) of 40/10, synthesis duration of 4 h, selenious acid concentration (C Se) of 80 mM, and reaction temperature of 120 °C. The highly crystalline structure of SeNPs in the hexagonal phase was characterized by powder X-ray diffraction (XRD) with a lattice parameter of 4.3 Å; meanwhile, their spheres with an average crystal size of 18.3 nm were estimated by high-resolution transmission electron microscope (HR-TEM). The rationale of bioreducing agents extracted from green orange peel for the formation of SeNPs was also recognized by Fourier-transform infrared spectroscopy (FT-IR). The antibacterial investigation of the SeNP sample was assessed against antibiotic-resistant bacteria, typically methicillin-resistant Staphylococcus aureus (MRSA), by executing the zone of inhibition and the minimum inhibitory concentration (MIC) tests. The SeNP sample demonstrated excellent antibacterial activity with an average diameter of inhibition zones of 20.0 ± 0.7 mm and an MIC of 4.94 µg/L. A comparison of the physicochemical properties of SeNPs synthesized from GOP extract by the hydrothermal method with SeNP products from other green reducing agents and other methods as well as its antibacterial activity compared with other nanoparticles and some antibiotics was conducted to highlight the superiority of GOP-mediated green-synthesized SeNPs.

Hydroxyapatite Derived from Salmon Bone As Green Ecoefficient Support for Ceria-Doped Nickel Catalyst for CO2 Methanation.

Hydroxyapatite (HA) derived from salmon bone byproducts is used as a green support for the nanostructured nickel catalysts applied in the methanation of carbon dioxide (CO2). Undoped nickel catalysts and various ceria-doped nickel supported on hydroxyapatite (HA) were prepared by coimpregnation. Characteristics of the as-prepared catalysts were investigated by the various techniques, including X-ray diffraction (XRD), scanning electron microscopy (SEM), Brunauer-Emmett-Teller (BET), hydrogen temperature-programmed reduction (H2-TPR), carbon dioxide temperature-programmed desorption (CO2-TPD), and energy-dispersive X-ray spectroscopy (EDX). The catalyst activity was assessed throughout CO2 methanation in the low-temperature range of 225-350 °C with the molar ratio of H2/CO2 = 4/1. The function of HA and ceria provided a high dispersity of nickel particles over the catalyst surface with the size range of 24.5-25.8 nm, leading to improvement in the reduction and CO2 adsorption capacity of the catalysts as well as enhancing the catalytic efficiency in CO2 methanation. The 10Ni/HA catalyst reduced at suitable conditions of 400 °C for 2 h showed the highest catalytic performance among the tested catalysts. CO2 conversion and CH4 selectivity reached 76.6 and 100% at a reaction temperature of 350 °C, respectively. The results show that the Ni/HA sample doped with 6.0 wt % ceria was the best, with the CO2 conversion and the CH4 selectivity reaching 92.5% and 100%, respectively, at a reaction temperature of 325 °C.

Insights into the effects of synthesis techniques and crosslinking agents on the characteristics of cellulosic aerogels from Water Hyacinth.

Aerogel cellulose materials were synthesised from Water hyacinth and different crosslinkers, such as kymene and a mixture of polyvinyl alcohol (PVA) and glutaraldehyde (GA). The effects of using a magnetic stirrer and ultrasonic methods were investigated. The results show that materials prepared using ultrasonic methods have higher porosity and lower density. The thermal conductivity of the synthesised aerogel cellulose could be as low as 0.0281 W m K-1, showing the good heat insulation performance of this material. Absorption capacity was tested using diesel oil (DO), and the highest capacities of 58.82 and 52.03 g g-1 of DO were found with kymene and PVA + GA as crosslinkers, respectively. The reusability of the materials was tested. After 10 cycles, the DO absorption capacity was 62.8% of the value of the first cycle for the aerogel cellulose sample with kymene as the crosslinker and 72.7% for the sample with PVA + GA as the crosslinking agent.