Modifications of Polymers through the Addition of Ultraviolet Absorbers to Reduce the Aging Effect of Accelerated and Natural Irradiation.

The photooxidative degradation process of plastics caused by ultraviolet irradiation leads to bond breaking, crosslinking, the elimination of volatiles, formation of free radicals, and decreases in weight and molecular weight. Photodegradation deteriorates both the mechanical and physical properties of plastics and affects their predicted life use, in particular for applications in harsh environments. Plastics have many benefits, while on the other hand, they have numerous disadvantages, such as photodegradation and photooxidation in harsh environments and the release of toxic substances due to the leaching of some components, which have a negative effect on living organisms. Therefore, attention is paid to the design and use of safe, plastic, ultraviolet stabilizers that do not pose a danger to the environment if released. Plastic ultraviolet photostabilizers act as efficient light screeners (absorbers or pigments), excited-state deactivators (quenchers), hydroperoxide decomposers, and radical scavengers. Ultraviolet absorbers are cheap to produce, can be used in low concentrations, mix well with polymers to produce a homogenous matrix, and do not alter the color of polymers. Recently, polyphosphates, Schiff bases, and organometallic complexes were synthesized and used as potential ultraviolet absorbers for polymeric materials. They reduced the damage caused by accelerated and natural ultraviolet aging, which was confirmed by inspecting the surface morphology of irradiated polymeric films. For example, atomic force microscopy revealed that the roughness factor of polymers' irradiated surfaces was improved significantly in the presence of ultraviolet absorbers. In addition, the investigation of the surface of irradiated polymers using scanning electron microscopy showed a high degree of homogeneity and the appearance of pores that were different in size and shape. The current work surveys for the first time the use of newly synthesized, ultraviolet absorbers as additives to enhance the photostability of polymeric materials and, in particular, polyvinyl chloride and polystyrene, based mainly on our own recent work in the field.

Sorption and degradation of ranitidine in soil: Leaching potential assessment.

Pharmaceuticals have been categorized as emerging contaminants that may be hazardous to the environment. To assess their environmental risk, understanding their fate and behaviour is highly needed, particularly in soil where little is known. This study investigated sorption, degradation and mobility potential of ranitidine (RAN) from soil to groundwater in two soils with different physicochemical properties. Sorption resulted in data were found to fit well to isotherm models following the order: linear model > Freundlich > Langmuir with R2 of up to 0.98. RAN showed low sorption affinity to soils with maximum adsorption coefficient (Kd) of 21.47 L kg-1. Physicochemical properties for soil and RAN showed insignificant positive correlation to Kd values except the sand%, which showed significant negative correlation. Degradation of RAN was fitted to the first order exponential decay model with minimum DT50 (time for a 50% dissipation in RAN concentration) values of 31.6 d under non-sterile conditions. Prolonged DT50 of 62.4 d was obtained in soils from sterile treatments indicating the microbial activity role in dissipation of RAN process. To predict potential leaching of RAN in soil, this study experimentally obtained values of Kd, Koc and DT50 were implemented in mathematical screening models. Results showed different but moderate leaching potential of RAN in soils.

Impact of stabilizer on the environmental behavior of PVC films reinforced 1,2,4-triazole moiety.

A new Schiff base containing 1,2,4-triazole ring system (L) was synthesized and confirmed by 1HNMR, FTIR spectroscopy. The chemical modification of PVC with a new Schiff base (L) was synthesized to produce a homogenous blend (PVC-L). A homogenous blend (PVC-L) was added to copper chloride to produce PVC-L-Cu (II). The PVC films had been irradiated with ultraviolet light for a long period and confirmed by FTIR spectroscopy and weight loss; the surface morphology was inspected by scanning electron microscopy.

Light-Switchable Self-Healing Dynamic Linear Polymers: Reversible Cycloaddition Reactions of Thymine-Containing Units.

A dynamic linear polymer was formed by the [2π+2π] reversible cycloaddition reaction of a thymine-based monomer under topochemical conditions and was used in self-healing applications. The reversible polymerisation of the thymine monomer was confirmed by UV and GPC analysis. Irradiation at 302 nm resulted in polymerisation of the monomer, and irradiation with wavelengths lower than 240 nm resulted in depolymerisation and the production of oligomeric units. This leads to a reduction in the glass transition temperature, and promoted healing of surface scratches due to the increased chain mobility. The self-healing ability of scratched samples was assessed based on the visual disappearance of the damage. In addition, the mechanical properties of the polymer before and after healing were found to be similar.