Improving the functionality of biodegradable food packaging materials via porous nanomaterials

Non-biodegradability and disposal problems are the major challenges associated with synthetic plastic packaging. This review article discusses a new generation of biodegradable active and smart packaging based on porous nanomaterials (PNMs), which maintains the quality and freshness of food products while meeting biodegradability requirements. PNMs have recently gained significant attention in the field of food packaging due to their large surface area, peculiar structures, functional flexibility, and thermal stability. We present for the first time the recently published literature on the incorporation of various PNMs into renewable materials to develop advanced, environmentally friendly, and high-quality packaging technology. Various emerging packaging technologies are discussed in this review, along with their advantages and disadvantages. Moreover, it provides general information about PNMs, their characterization, and fabrication methods. It also briefly describes the effects of different PNMs on the functionality of biopolymeric films. Furthermore, we examined how smart packaging loaded with PNMs can improve food shelf life and reduce food waste. The results indicate that PNMs play a critical role in improving the antimicrobial, thermal, physicochemical, and mechanical properties of natural packaging materials. These tailor-made materials can simultaneously extend the shelf life of food while reducing plastic usage and food waste.     

[Hmim][HSO4], a Green and Recyclable Acidic Ionic Liqiud Medium for the One‐Pot Nitration of TADB to HNIW

An efficient and mild procedure for the one‐pot preparation of CL‐20 from TADB in the presence of the Brønsted acidic ionic liquid 1‐methylimidazolium hydrogen sulfate [Hmim][HSO₄] as catalyst was developed. The ionic liquid was stable during the reaction process and could also be reused several times with steady activity. In order to optimize the process parameters to obtain higher yield and purity, a study was carried out with variation of the ionic liquids and some parameters like temperature, mole ratio of [Hmim][HSO₄] and nitric acid. This procedure may be a practical alternative to the existing procedures to meet the nees of academics as well as industry.     

Effect of apple cider vinegar agent on the microstructure,phase evolution,and magnetic properties of CoFe2O4 magnetic nanoparticles

In the present study, spinel structure CoFe₂O₄ nanoparticles were successfully synthesized by the sol-gel auto-combustion technique. The effect of apple cider vinegar (ACV) addition as an organic biocompatible agent on the size, morphology, and magnetic properties of CoFe₂O₄ nanoparticles was investigated in detail. The phase evolution, particle size, and lattice parameter changes of the synthesized phase have been estimated by using Rietveld structure refinement analysis of X-ray powder diffraction data. Also, Fourier transform infrared spectra (FT-IR) of the samples verified the presence of two expected bands correspond to tetrahedral and octahedral metal-oxygen complexes within the spinel structure. Furthermore, microstructural observations revealed that ultrafine particles have a semi-spherical morphology. It was shown that the particles size decreased from ~45 to ~17 nm with an increase in the amount of ACV. Magnetic properties were carried out by vibrating sample magnetometer (VSM) at room temperature. Both the saturation magnetization (M_s) and coercivity (H_c) were found to be significantly dependent on the crystallite size and the amount of ACV.     

Electro-conductivity,bioactivity and UV protection of graphene oxide-treated cellulosic/polyamide fabric using inorganic and organic reducing agents

Here, graphene oxide (GO) was treated on the cellulosic/polyamide fabric reduced with various inorganic and organic compounds and compared the color changes, field emission scanning electron microscopy, energy-dispersive X-ray spectroscopy, X-ray diffraction, electrical resistivity, antibacterial/antifungal and ultraviolet protection properties. The graphite oxide was first synthesized using graphite and sonicated to obtain GO. It was then dissolved in distilled water along with cetyltrimethylammonium bromide (CTAB) to prepare a stable solution for long-time adsorbing more and uniform GO on cellulosic/polyamide fabric through exhaustion method. The GO-treated fabric was reduced to reduced graphene oxide (rGO) with inorganic and organic reducing agents including sodium dithionite with and without sodium hydroxide and dopamine hydrochloride at various temperatures. More fabricated GO reduced to rGO at higher temperature using dopamine produced lower electrical resistance. The antimicrobial activities of various samples were tested against two Gram-negative bacteria, E. coli and P. aeruginosa, two Gram-positive bacteria, S. aureus and E. faecalis and one eukaryotic fungus C. albicans. Ultraviolet protection was examined through reflectance spectra showed no UV transmittance from most of the treated fabrics. Further, CTAB was effective to load more GO on the fabric improved electrical resistance and higher antibacterial properties using both reducing agents.     

Polyvinylpolypyrrolidone-Supported Chlorosulfonic Acid: An Efficient Catalyst for One-Pot Synthesis of Dihydropyrimidinones and Octahydroquinazolin-2,5-diones

Polyvinylpolypyrrolidone-supported chlorosulfonic acid has been successfully applied to perform one-pot reaction of arylaldehydes, urea, ethylacetoacetate, or cyclic 1,3-diketo compounds under solvent-free condition at 70°C to provide a series of dihydropyrimidinones and octahydroquinazolin-2,5-diones in good to excellent yields. The method offers several advantages such as high yield, short reaction time, simple workup, easy preparation, and reusability of the catalyst. The [PVPP-SO₃H]⁺Cl^? catalyst was characterized via Fourier transform infrared spectroscopy (FT-IR) and thermal gravimetric analysis (TGA). Moreover, the catalyst could be recycled several times without significant loss of its catalytic activity. Clean methodologies, easy work-up procedure, high yield, and simple preparation of the catalyst are some advantages of this article.     

Equilibrium and kinetic studies of azo dye (Basic Red 18) adsorption onto montmorillonite: Numerical simulation and laboratory experiments

Adsorption of BR 18 dye onto nano-clay adsorbent was investigated. Nano-clay was characterized by using FTIR, SEM, TEM, XRD and BET analysis. The percent removal increased by increasing nano-clay dose, while pH and stirring speed had no significant effect on the adsorption rate. It was observed that the uptake of dye onto nano-clay initially increased rapidly, and then decreased slowly until the equilibrium was reached. The adsorption capacity rose with an increase in temperature. Moreover, the adsorption kinetics was very fast and followed a pseudo second-order. The intra-particle diffusion was observed to be the rate-controlling step. In addition, equilibrium data fitted well with the Langmuir adsorption model. This paper also presents a numerical simulation incorporating the second-order kinetic expression using COMSOL Multiphysics software. The numerical modelling results and the experimental data were in excellent agreement.     

The sorption of monovalent cations onto norway spruce: Model studies using wood flour and LiCl solution

The transport of chemicals in a porous material such as wood is very complex and involves several processes: the diffusion of chemicals in the cell pores (lumen and pit pores), through the cell walls at certain conditions, and sorption of wood tissue. In the present study, batch sorption experiments were performed to examine the sorption of Li⁺ ions from an aqueous LiCl solution onto Norway spruce wood flour samples. The experimental methodology employed is suitable for differentiating the amount of ions sorbed onto the wood tissue and dissolved in the solution in wood pores. The apparent equilibrium sorption data were analyzed using two widely applied isotherm models: Langmuir and Freundlich. The results suggest that the sorption was spontaneous, and for the experimental conditions studied, probably involved several interaction types between the different functional groups of the wood and the Li⁺/Cl^? ions.     

Application of thermal ultrasound-assisted liquid–liquid micro-extraction coupled with HPLC-UV for rapid determination of synthetic phenolic antioxidants in edible oils

A simple, fast, and reliable liquid–liquid micro-extraction (LLME) method assisted by thermal ultrasound approach was developed for simultaneous determination of synthetic phenolic antioxidants (SPAs) in edible oils by high-performance liquid chromatography equipped with ultraviolet detector (HPLC-UV). The synthetic antioxidants were propyl gallate (PG), butylated hydroxyanisole (BHA), tert-butylhydroquinone (TBHQ), and butylated hydroxyltoluene (BHT). The best extraction conditions were observed were methanol/acetonitrile (1:1, v/v) as the solvent, ultrasound at 4 min, and a temperature of 40°C. The linearity of the calibration curves for the optimum conditions were R² > 0.989 for all of the SPAs in a range from 1–200 μg ml⁻¹. Relative standard deviation (RSD %) for five analysis was in range of 2.83% to 4.21%. Limit of detection (LOD) and limit of quantification (LOQ) were obtained in range of 0.012–0.06 and 0.04–0.2 μg g⁻¹, respectively. With regard to recovery, a range of 91%–116% was calculated for the spiked edible oils.