The microparticle content of 37 common facial and body scrubs commercially available in the United Arab Emirates was analyzed. The chemical composition, ash content, physical characteristics, loading, particle size and shape of the microparticles were determined. Only 11 out of 37 products were found to have microplastic content. Many of the remaining products exhibited microparticles composed of microcrystalline cellulose and crushed walnut shells. Differential scanning calorimetry showed that microplastic products had softening points as low as 84 °C. Plastic microbeads of 2 products were found to fuse at 100 °C. The fusion altered the flotation characteristics of the microbeads of one product. Heat treatment of the product at 100 °C in the presence of silica gel led to entrainment of the silica and partial fragmentation of the beads upon cooling. This may be understood as one mechanism of fragmentation of a microplastic with a low softening point in the presence of hard soil particles under temperature cycling.

It is necessary to better characterize plastic marine debris in order to understand its fate in the environment and interaction with organisms, the most common type of debris being made of polyethylene (PE) and polypropylene (PP). In this work, plastic debris was collected in the North Atlantic sub-tropical gyre during the Expedition 7th Continent sea campaign and consisted mainly in PE. While the mechanisms of PE photodegradation and biodegradation in controlled laboratory conditions are well known, plastic weathering in the environment is not well understood. This is a difficult task to examine because debris comes from a variety of manufactured objects, the original compositions and properties of which vary considerably. A statistical approach was therefore used to compare four sample sets: reference PE, manufactured objects, mesoplastics (5–20 mm) and microplastics (0.3–5 mm). Infrared spectroscopy showed that the surface of all debris presented a higher oxidation state than the reference samples. Differential scanning calorimetry analysis revealed that the microplastics were more crystalline contrarily to the mesoplastics which were similar to references samples. Size exclusion chromatography showed that the molar mass decreased from the references to meso- and microplastics, revealing a clear degradation of the polymer chains. It was thus concluded that the morphology of marine microplastic was much altered and that an unambiguous shortening of the polymer chains took place even for this supposedly robust and inert polymer.

Microplastic pollution has gained significant attention, and there are growing concerns about its potential effects on aquatic environments. The lack of proper solid waste management in Egypt has resulted in the accumulation of plastic litter and its deposition in waterways. However, no attempts have been made to identify or assess marine plastic litter in Egypt. We provide, for the first time, a precise, simple, and cost-effective method to identify microplastics in Eastern Harbor by using differential scanning calorimetry (DSC). This screening revealed the presence of ten polymers in seawater and shoreline sediments. Most of the extracted microplastics are secondary microplastics, as they appear to be remnants of larger plastic fragments.

Fibrous mats of polymer/clay were obtained by electrospinning method, and their capacity for heavy metals removal from water was evaluated. Four different fibrous mats were prepared from a corresponding polymer/clay solutions. The precursor materials employed were poly-ε-caprolactone, polyvinyl alcohol polymers, kaolin, and metakaolin clays. Raw materials and the prepared fiber mats characterization were carried out using scanning electron microscopy, Fourier transformed infrared spectroscopy, X-ray diffraction, termogravimetric analysis, differential thermal analysis, and differential scanning calorimetry. Elemental composition of the materials was obtained using energy-dispersive X-ray spectroscopy. The environmental applications of polymer/clay materials were tested for water treatment by heavy metals (cadmium (Cd⁺²), chromium (Cr⁺³), copper (Cu⁺²), and lead (Pb⁺²)) sorption. Kinetic adsorption studies were conducted employing heavy metal solutions with initial concentration of 200 mg/L, and the amount of heavy metal adsorbed and kinetics parameters was determined using inductively coupled plasma-optical emission spectroscopy (ICP-OES). According to the kinetic data, the adsorption process of Cd⁺², Cr⁺³, Cu⁺², and Pb⁺² onto polymer/clay is favorable for the prepared materials and they follow a pseudo-first-order model according to the kinetic analysis. Additionally, the intraparticle diffusion was evaluated by applying the Morris and Weber model; in order to investigate the contribution of film resistance to the kinetics of the heavy metals adsorption, the adsorption kinetic data was further analyzed by Boyd’s film-diffusion model.

A series of aluminum oxyhydroxide-incorporated titania composites were prepared by a one-pot synthetic procedure using aluminum tri-sec-butoxide as a precursor. The as-synthesized samples were characterized by Fourier transform infrared spectrophotometer, X-ray diffraction, thermogravimetry and differential scanning calorimetry, nitrogen physisorption, and scanning electron microscopy. It was identified that aluminum oxyhydroxide (γ-AlOOH, or boehmite) was produced as aluminum matrix into which titania, commercially available P25, was incorporated. Photocatalytic activity of all nanocomposites was evaluated with respect to the photodecolorization of methyl orange under UV irradiation and almost complete decolorization was eventually achieved under optimum experimental conditions.

Biodegradable polymer poly(3-hydroxybutyrate) (P3HB) has been used as a matrix to construct slow-release formulations of the fungicide tebuconazole (TEB). P3HB/TEB systems constructed as films and pellets have been studied using differential scanning calorimetry, X-ray structure analysis, and Fourier transform infrared spectroscopy. TEB release from the experimental formulations has been studied in aqueous and soil laboratory systems. In the soil with known composition of microbial community, polymer was degraded, and TEB release after 35 days reached 60 and 36 % from films and pellets, respectively. That was 1.23 and 1.8 times more than the amount released to the water after 60 days in a sterile aqueous system. Incubation of P3HB/TEB films and pellets in the soil stimulated development of P3HB-degrading microorganisms of the genera Pseudomonas, Stenotrophomonas, Variovorax, and Streptomyces. Experiments with phytopathogenic fungi F. moniliforme and F. solani showed that the experimental P3HB/TEB formulations had antifungal activity comparable with that of free TEB.

Use of sodium chloride to preserve animal skins and hides is becoming increasingly untenable due to stringent environmental regulations. In the present research work, a combination of sparingly soluble alkali and water-soluble polymer of ethylene oxide has been used to preserve skins with an objective of total elimination of common salt for preservation. A comprehensive study has been made for evaluating various parameters, such as dehydration and rehydration behaviours of skins, microbial growth, emission loads and physico-chemical characteristics of the cured skin to validate the salt-free preservation system developed. The shrinkage temperature, denaturation temperature and mechanical strength of tanned leather were analysed by using shrinkage, differential scanning calorimetric and thermomechanical analysis techniques. The new curing system has been found to be effective in preserving the skin as indicated by the various parameters studied and the final leather quality. The significant reduction in total solids content such as dissolved solids and suspended solids present in the effluent compared to conventional preservation method is evident from environmental impact assessment studies.

There are several techniques used to analyze microplastics. These are often based on a combination of visual and spectroscopic techniques. Here we introduce an alternative workflow for identification and mass quantitation through a combination of optical microscopy with image analysis (IA) and differential scanning calorimetry (DSC). We studied four synthetic polymers with environmental concern: low and high density polyethylene (LDPE and HDPE, respectively), polypropylene (PP), and polyethylene terephthalate (PET). Selected experiments were conducted to investigate (i) particle characterization and counting procedures based on image analysis with open-source software, (ii) chemical identification of microplastics based on DSC signal processing, (iii) dependence of particle size on DSC signal, and (iv) quantitation of microplastics mass based on DSC signal. We describe the potential and limitations of these techniques to increase reliability for microplastic analysis. Particle size demonstrated to have particular incidence in the qualitative and quantitative performance of DSC signals. Both, identification (based on characteristic onset temperature) and mass quantitation (based on heat flow) showed to be affected by particle size. As a result, a proper sample treatment which includes sieving of suspended particles is particularly required for this analytical approach.

Sulfur extraction from fuel is essential to be done for environmental and industrial point of view. Extractive desulfurization (EDS) is one of the most promising techniques in order to achieve legislative sulfur content requirements. Among numerous extractants and solvents, ionic liquids (ILs) are more capable due to their desirable green solvent properties. This work demonstrated that trihexyl(tetradecyl)phosphonium tetrafluoroborate ([THTDP]BF₄) was synthesized, characterized, and employed as extraction solvent for extraction of dibenzothiophene (DBT), thiophene, benzothiophene, and other alkyl-substituted derivatives of sulfur from liquid fuel. Molecular confirmation and purity of synthesized ([THTDP]BF₄) were analyzed with FTIR, Raman, NMR, EPR, UV, TG/DSC, and XRD analyses. Also, physical properties of ([THTDP]BF₄) were carried out. The effects of extraction time, temperature, sulfur compounds, ultra-sonication, and ([THTDP]BF₄) recycling/regeneration on DBT removal from liquid fuel were also examined. DBT removal in n-dodecane was 92.6% using EDS with mass ratio (1:1) in 30 min at 30 °C under the mild reaction conditions. ([THTDP]BF₄) could be reused up to ten cycles for sulfur extraction and regenerated for few more cycles with good DBT removal ability. Also, the sulfur extraction from real fuels and multistage extraction performance were tested. The experimental data and results provided in this article discover the remarkable understandings of tetrafluoroborate-based phosphonium ionic liquids as promising solvent for EDS.