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      Long-Term Effect of Ultraviolet Irradiation on Poly(vinyl chloride) Films Containing Naproxen Diorganotin(IV) Complexes

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          Abstract

          As poly(vinyl chloride) (PVC) photodegrades with long-term exposure to ultraviolet radiation, it is desirable to develop methods that enhance the photostability of PVC. In this study, new aromatic-rich diorganotin(IV) complexes were tested as photostabilizers in PVC films. The diorganotin(IV) complexes were synthesized in 79–86% yields by reacting excess naproxen with tin(IV) chlorides. PVC films containing 0.5 wt % diorganotin(IV) complexes were irradiated with ultraviolet light for up to 300 h, and changes within the films were monitored using the weight loss and the formation of specific functional groups (hydroxyl, carbonyl, and polyene). In addition, changes in the surface morphologies of the films were investigated. The diorganotin(IV) complexes enhanced the photostability of PVC, as the weight loss and surface roughness were much lower in the films with additives than in the blank film. Notably, the dimethyltin(IV) complex was the most efficient photostabilizer. The polymeric film containing this complex exhibited a morphology of regularly distributed hexagonal pores, with a honeycomb-like structure—possibly due to cross-linking and interactions between the additive and the polymeric chains. Various mechanisms, including direct absorption of ultraviolet irradiation, radical or hydrogen chloride scavenging, and polymer chain coordination, could explain how the diorganotin(IV) complexes stabilize PVC against photodegradation.

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          Surface-modified antibacterial TiO2/Ag+ nanoparticles: Preparation and properties

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            Structural and mechanistic aspects of the thermal degradation of poly(vinyl chloride)

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              Biodegradation of different formulations of polyhydroxybutyrate films in soil

              Background Petroleum polymers contribute to non-degradable waste materials and it would therefore be desirable to produce ecofriendly degradable materials. Biodegradation of polyhydroxybutyrate (PHB) in the presence of oligomer hydrolase and PHB depolymerase gave 3-hydroxybutyric acid which could be oxidized to acetyl acetate. Several bacteria and fungi can degrade PHB in the soil. Results Biodegradation of PHB showed a significant decrease in the molecular weight (Mw), number-average molecular weight (Mn) and the dispersity (Mw/Mn) for all the film formulations. Nanofibers of PHB and its composites showed faster degradation compared to other films and displayed complete degradation after 3 weeks. The SEM micrographs showed various surface morphology changes including alterations in appearance of pores, cavity, grooves, incisions, slots and pointers. Such changes were due to the growth of microorganisms that secreted PHB depolymerase enzyme which lead to the biopolymer films degradation. However, PHB nanofibers and its composites films in the presence of TiO2 demonstrated more surface changes with rupture of most nanofibers in which there was a drop in fibres diameter. Conclusions The degradation of biopolymers help to overcome some of the pollution problems associated with the use of petroleum polymers. PHB nanofiber and its TiO2 composite were degraded faster compared to other PHB film types due to their three dimensional and high surface area structures. The presence of TiO2 nanoparticles in the composite films slowdown the degradation process compared to PHB films. Additionally, the PHB and its composite films that were prepared from UV treated PHB films led to acceleration of the degradation. Graphical abstract Biodegradation of polyhydroxybutyrate films in soil
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                Author and article information

                Journal
                Molecules
                Molecules
                molecules
                Molecules
                MDPI
                1420-3049
                28 June 2019
                July 2019
                : 24
                : 13
                : 2396
                Affiliations
                [1 ]Department of Chemistry, College of Science, Babylon University, Babil 51002, Iraq
                [2 ]Department of Chemistry, College of Science, Al-Nahrain University, Baghdad 64021, Iraq
                [3 ]Department of Optometry, College of Applied Medical Sciences, King Saud University, P.O. Box 10219, Riyadh 11433, Saudi Arabia
                [4 ]Department of Medical Instrumentation Engineering, Al-Mansour University College, Baghdad 64021, Iraq
                [5 ]National Center for Petrochemicals Technology, King Abdulaziz City for Science and Technology, P.O. Box 6086, Riyadh 11442, Saudi Arabia
                [6 ]Department of Physics, College of Science, Al-Nahrain University, Baghdad 64021, Iraq
                Author notes
                [* ]Correspondence: emad_yousif@ 123456nahrainuniv.edu.iq (E.Y.); gelhiti@ 123456ksu.edu.sa (G.A.E.-H.); mhhalotaibi@ 123456kacst.edu.sa (M.H.A.); Tel.: +966-11469-3778 (G.A.E.-H.); Fax: +966-11469-3536 (G.A.E.-H.)
                Author information
                https://orcid.org/0000-0002-5396-7560
                https://orcid.org/0000-0003-1458-4724
                https://orcid.org/0000-0001-6675-3126
                https://orcid.org/0000-0001-5435-5200
                Article
                molecules-24-02396
                10.3390/molecules24132396
                6650850
                31261834
                94eb737a-4160-4726-ad59-04dffaa5acdc
                © 2019 by the authors.

                Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license ( http://creativecommons.org/licenses/by/4.0/).

                History
                : 26 May 2019
                : 28 June 2019
                Categories
                Article

                naproxen,poly(vinyl chloride) films,diorganotin(iv) complexes,photodegradation,photostabilizer,synthesis

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