Ultraviolet (UV) light has harmful effects on materials used in outdoor applications. Plastics suffer photooxidation when exposed to harsh conditions (high temperature, sunlight for long duration, and humidity) in the presence of oxygen. Plastic degradation, as a result of UV light absorption, leads to discoloration, cracks, and loss of mechanical and physical properties ^[1][2][1,2]. Photooxidation resembles autooxidation due to long-term heat aging, except that the driving force is UV light and not heat [3]. Therefore, during plastic manufacturing, measures should be taken to ensure that the materials will last longer and to inhibit photooxidation and photodegradation processes.

The polymerization technique was developed over the years to allow the production of plastics on an industrial scale. There has been a massive increase in the production of plastics in recent years [4]. The scale of polyvinyl chloride (PVC) production has increased over the years from 3 million tons in 1965 to over 40 million tons in 2018 and is expected to grow further to 60 million tons in 2025 [5]. PVC can be produced in different forms and shapes, using both suspension and emulsion polymerization [6]. Plastic waste is a challenge, and there is a need for not only effective recycling but cutting the waste at the source. Therefore, further developments in plastic are still needed to keep the environment clean and to elongate the lifetime of plastic ^[7][8][7,8].

Plastic contains polymeric chains that are based on carbon, hydrogen, and heteroatoms (e.g., sulfur, oxygen, or nitrogen). Polystyrene (PS), polypropylene (PP), polyethylene (PE), PVC, polyethylene terephthalate (PET), and polyurethane (PU) represent 75–80% of Europe’s plastic consumption (Table 1) ^[9][10][9,10]. These polymers have either C–C or C–heteroatom backbones, and their properties are highly dependent on the repeating units [11].

Plastics are highly involved in our daily lives, from household items to very complex medical equipment. They are used in construction materials (e.g., windows, panels, glazing, coatings, siding, roofing, flooring, fencing, and decoration), furniture, offices, agriculture (e.g., mulch film, materials for greenhouses, and production of sacks), transportation (e.g., bodywork and production of protective coatings), flame and smoke retardants (high content of chlorine; 57% by weight), insulators, and others [6]. Polycarbonate plastic has a low thermal conductivity (k) and, therefore, is better than conventional glazing agents [12]. The demand for plastic has extensively increased due to its unique mechanical and physical properties (e.g., light weight, strength, resistance to corrosion and chemicals) and low manufacturing cost. In addition, the shape and properties of plastics can be manipulated based on the application. However, UV radiation has a negative effect on plastic (e.g., rigid PVC) lifetime and leads to the loss of its strength. The solar irradiation of PVC causes discoloration and the emission of toxic volatiles, which hinders its use in outdoor applications [13]. PVC is still used as a construction material, but it can be replaced by polyolefins, which are less harmful but cost more.

The degradation of plastics is of major concern from an environmental perspective in terms of potential hazards to living organisms. The degradation of plastics takes place under either abiotic or biotic (e.g., biodegradation) conditions [14]. Biodegradation is highly dependent on environmental factors, which vary based on the type of polymer. Color changes and the crazing of plastic are early signs of degradation, followed by surface cracking and the formation of small fragments [15]. Floating plastics in seas and oceans are moderately affected by temperatures, solar radiation, and oxygen through photoinitiated oxidative degradation. For abiotic degradation, the contributing factors are sunlight and oxygen, and they affect the plastic through a hydrolysis process [16].

Three steps (initiation, propagation, and termination) are involved in plastic degradation [17]. The first step is initiated through solar or thermal initiators and leads to the formation of free radicals. Photoinitiation is not likely for both PE and PP, since they do not have unsaturated chromophores in their skeletons that are responsible for the absorption of light [18]. Impurities or abnormalities within plastics allow for the production of free radicals leading to C–H bonds cleavage in the backbone of polymers ^[19][20][19,20]. In the presence of oxygen, free radicals produce peroxy reactive moieties in the propagation step. In addition, hydroperoxides can be produced, leading to the autoxidation of polymers [21]. In the propagation step, crosslinking or chain scission takes place [22]. The deactivation of free radicals occurs in the termination step, leading to stable products. In the presence of oxygen, the formation of oxygen-containing moieties is expected, which leads to a photoinitiated degradation process. The chain scission and crosslinking (termination) of oxygenated species leads to the formation of olefins (unsaturated polymeric chains), aldehydes, and ketones (Figure 1) [23].

Plastic natural degradation is initiated through photodegradation followed by thermo-oxidative degradation [24]. Sun UV light provides the energy needed to initiate the incorporation of oxygen into the polymeric chains [25]. Plastics are degraded to small polymeric fragments and then metabolized by microorganisms in the surrounding environment. Microorganisms tend to convent the polymeric chain carbons to either carbon dioxide or biomolecules ^[26][27][26,27]. However, such a process is very slow (taking up to 50 years) for the complete degradation of plastics [28]. Chromophores present within the skeleton of polymers absorb visible or UV light, and therefore initiate the photodegradation process ^[29][30][29,30]. Photodegradation takes place either in the presence of oxygen (e.g., photooxidation) or in its absence (e.g., chain crosslinking or bond breaking). When polymers (e.g., polyolefins) are exposed to heat, UV light, or mechanical stress in the presence of oxygen, they produce free radicals that initiate the oxidation process. Therefore, plastics should be stabilized to inhibit the oxidative processes to increase the half-life time of materials [31].

Plastic weathering involves changes in the physical, mechanical, and chemical properties of polymers, particularly at the surface [32]. Solar energy, moisture (e.g., rain, snow, or humidity), oxidants (e.g., ozone or atomic or singlet oxygen), and air pollutants (e.g., sulfur dioxide, nitrogen oxides, or polycyclic hydrocarbons) are responsible for these changes [33]. Uneven discoloration, surface cracks, or loss of strength are the most common changes within plastics due to degradation [34]. Climate change and the rise in global temperatures accelerate polymers’ weathering, and impurities (e.g., traces of metals or oxidants) present in additives increase the rate of photodegradation [35].

PVC is a synthetic plastic that is similar to PP, but the backbone carbons are attached to chlorine atoms instead of hydrogens. PVC is one of the most common manufactured plastics [36]. Due to the high content of chlorine, PVC is hard and stiff. In addition, PVC is polar due to the presence of C–Cl bonds and is soluble in many solvents, particularly those containing polar atoms such as ethers (e.g., dioxane, tetrahydrofuran, ketones, or nitrobenzene). It has a low cost, is durable, has excellent performance, is easily molded, and can be obtained in different shapes that are suitable for many applications. PVC is commonly used in packaging, health care devices, toys, construction materials, electrical wire insulation, clothes, and furnishing ^[5][6][5,6]. For outdoor applications, PVC photostability should be enhanced through the addition of suitable additives to inhibit its photodegradation. The dechlorination of PVC is autocatalytic, which leads to the formation of –C=C–. The formation of unsaturated double bonds within the backbone of PVC leads to its photodegradation, in which small fragments and polyene residues are produced (Figure 2) [37].

Plastic recycling has received attention recently due to the large volume of waste that it generates [38]. Pyrolysis and incineration of PVC are not recommended due to the high level of hydrogen chloride (HCl) and other toxic volatiles produced [39]. The most common methods for PVC recycling include chemical and mechanical techniques. Mechanical recycling is preferred when the PVC waste composition is known [40]. On the other hand, the chemical recycling of PVC converts plastics back to chemicals that can be reused in the polymerization process. The development of techniques and instrumentation for the separation of PVC from the waste stream is still important to allow for the recovery of most wasted PVC.

2. Photostabilization of Polymers Using UV Absorbers

UV absorbers play an important role in absorbing harmful radiation from light and dissipating it as harmless thermal energy ^[41][42][43][41,42,43]. In addition, they block the formation of free radicals that are produced at the early stages of degradation. The most common industrial UV absorbers are titanium oxide, carbon black, benzophenones, and triazoles (e.g., hydroxylbenzophenone and hydroxyphenylbenzotriazole), while the most common additives used recently for research include Schiff bases and organometallic complexes (Figure 3).

Figure 3. Structures of some common UV absorbers.

These additives have unique UV absorbance characteristics. For example, benzophenone-containing additives absorb UV strongly in the short-wavelength region through a proton transfer or tautomeric structure equilibrium (Figure 4). They are more efficient compared with the additives containing benzotriazole. Benzophenone-based UV absorbers have unique properties such as low cost, low toxicity, and good resistance to water and acids [44].

Figure 4. Hydroxybenzophenones energy dissipation through a proton transfer.

Triazoles have high molar extinction coefficients (5 × 10⁶ cm⁻¹M⁻¹) and absorb the most destructive wavelength of light (280–370 nm), which is highly involved in polymer degradation. The excitation of benzotriazoles takes place once the UV light is absorbed; the benzotriazoles then dissipate the energy through either heat release, involving a hydrogen transfer, or fluorescence emission ^[45][54]. In addition, UV absorbers act as quenchers (Q) for the triplet excited state of the polymer chromophoric group (P *), followed by the release of energy as harmless heat (Figure 5) [46]. Similarly, metal complexes act as effective UV quenchers due to their low excitation coefficients and quench the triplet state of the carbonyl groups in polyolefins ^[47][48][49][47,48,49].

Figure 5. UV absorbers act as quenchers for the excited state energy of polymers. * Represents the excited state.

Recently, we synthesized a range of UV stabilizers (e.g., aromatics, heterocycles, Schiff bases, organometallic complexes, and polyphosphates) and tested their efficiency for the stabilization of polymers ^{[50][51][52][53][45][54][55][56][57][58][59][60][61][62][63][64][65][66][67][68][69][70][71][72][73][74][75][76][77][78][79][80][81][82][83][84]}[50,51,52,53,54,55,56,57,58,59,60,61,62,63,64,65,66,67,68,69,70,71,72,73,74,75,76,77,78,79,80,81,82,83,84,85]. These additives, at a low concentration of 0.5% by weight, led to a significant improvement in the photostability of polymers. The stabilization effect that the UV absorbers induced in polymers was examined using infrared spectroscopy, the determination of weight and molecular weight, and inspection of the surface of polymers.

In conclusion, polymer stabilization is one of the most important processes that is used to elongate the lifetimes of plastic products. Plastics used in outdoor applications suffer in harsh environments and quickly lose their mechanical and physical properties. The proper solution for inhibiting the photooxidation of plastics due to the inevitable exposure to light and oxygen is through the addition of efficient ultraviolet absorbers that are capable of acting as efficient scavengers for light and blocking the formation of free radicals within the polymeric chains. The additives should absorb irradiation light directly and decompose peroxide species. In addition, they should be very compatible with the polymers, not alter the color, be used at a very low concentration, and be safe for the environment if released. Progress was made with the design and use of safe additives to enhance plastic stability and, in particular, polystyrene and polyvinyl chloride. Polyphosphates, Schiff bases, and organometallic complexes containing aromatic moieties showed the potential to be used as ultraviolet absorbers for plastics. The damage on the surface of irradiated plastics in the presence of ultraviolet absorbers is low compared with the blank films.

Since the additives are not linked to plastic through covalent bonds, they can be leached to the surrounding environments. The leakage of these chemicals followed by their degradation poses a danger to both animals and humans. Therefore, future research should be attention to the design, synthesis, and use of safe, non-toxic, and highly stable polymeric additives to suppress the degradation of plastic. Some progress was made, but there is still room for further improvements and modifications.

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