Photodegradation of plasticized poly(vinyl chloride) (PVC) stabilized by different thermal stabilizers including organic calcium complex and mercaptide organotin was investigated. Plasticized PVC sheets prepared by an open twin-roller mill and plate vulcanizing machine were exposed to xenon-arc light with the irradiance of 0.51 W/ (m 2 Ánm) at 658C. A much better color stability displayed by mercaptide organotin than organic calcium complex has been confirmed by digital photos and color difference. This can be explained that the more effective mercaptide organotin minimizes the amount of thermal damage from processing thus favours subsequent UV weathering. Carbonyl index and decomposition activation energy (E a1 ) obtained from attenuated total refection-Fourier transform infrared spectra (ATR-FTIR) and thermogravimetric (TG) analysis, respectively, further indicate that plasticized PVC sheets containing mercaptide organotin have more excellent UV resistance. Mechanical tests reveal that photodegradation of PVC is accompanied by the predominant process of chain scission on the surface of samples. POLYM. ENG. SCI., 51:624-631, 2011. ª
The effect of the combination of a UV absorber (Chimassorb 81) with different types of thermal stabilizers, including an organic calcium complex and an organotin mercaptide, on the photodegradation of poly(vinyl chloride) (PVC) was investigated by color difference measurements, UV-Vis spectroscopy, Fourier-transform infrared spectroscopy, thermogravimetric (TG) analysis, and viscosity-average molecular weight determination. Films of PVC containing 0.5 phr of Chimassorb 81, with and without 2 phr of a thermal stabilizer, were prepared by solution casting. Then the accelerated UV weathering of the films was carried out under xenon light with an irradiance of 0.51 W/(m 2 Á nm) at 658C. The results showed that both Chimassorb 81 and the mixture of Chimassorb 81 with the organic calcium complex showed good behavior in inhibiting the photodehydrochlorination and photooxidation of PVC. In contrast, the combination of Chimassorb 81 and methyltin mercaptide significantly accelerated initial color development during the final 200 h of exposure because of the UV sensitivity of the organotin. Moreover, when Chimassorb 81 and the methyltin mercaptide were used together to stabilize PVC films, the expected antioxidant effect of the mixture was not observed, in contrast to the behavior found with other stabilized systems, perhaps because the Chimassorb 81 had been depleted by the methyltin mercaptide during the UV irradiation. The TG analysis revealed that ultraviolet irradiation had caused severe destruction of the PVC chains. However, addition of Chimassorb 81 or the combination of Chimassorb 81 with the organic calcium complex effectively prevented the destruction, as was demonstrated by changes in the activation energies for thermal degradation.
The combined effect of a basic hindered amine light stabilizer (HALS) and ultraviolet absorbers (UVAs) on casted poly(vinyl chloride) (PVC) films, during photodegradation, was studied by color change, ultraviolet‐visible (UV–vis) spectroscopy, Fourier‐transform infrared (FTIR) spectroscopy, and viscosity‐average molecular weight. It was found that the basic amine groups in the HALS (T770) could promote the dehydrochlorination, thereby accelerating the photooxidation of PVC films. Meanwhile, T770 could scavenge the radicals formed and restrain the aging of PVC to some extent. The above‐mentioned aspects were competing factors: the former played a dominant role during the first 100 h, while the latter counteracted the former effect to some extent between 100 and 300 h. A benzotriazole derivative (UV326) absorbs more UV radiation in the UV‐A region (320–400 nm), which mainly causes the photodegradation of PVC samples, than a benzophenone derivative (UV531). Thus, UV326 is a more efficient UV absorber than UV531 in prohibiting the photooxidation and chain scission of PVC films. The combination of T770 and UV326 effectively protected PVC films from dehydrochlorination and photooxidation. The combination of T770 and UV531 accelerated the dehydrochlorination and discoloration of PVC films. J. VINYL ADDIT. TECHNOL., 2012. © 2012 Society of Plastics Engineers
The photostability of hindered amine light stabilizer (HALS) and ultraviolet absorber (UVA) on the blends of plasticized poly (vinyl chloride) (PVC) and powder nitrile rubber (NBR) has been studied with a Xenon Test Chamber. The digital photos, color differences, attenuated total refection‐Fourier transform infrared (ATR‐FTIR) spectra and mechanical properties of the blends have been determined. HALS combined with UVA effectively protects PVC/NBR blends from yellowing and restrains the decrease of elongation at break of the blends. The synergistic phenomenon is ascribed to the different photostable mechanisms of HALS and UVA at different photo aging stages. The color of PVC/NBR control sample quickly changes into yellow at the first 400 h of irradiation, due to the polyenes structures that induced by the double bonds of butadiene in NBR. From 400 to 800 h, crosslinking dominates and the amount of polyenes decreases, resulting into the decrease of color change. At the early stage of irradiation, chain‐scission of polymer takes the predominant place, and the tensile strength decreases. But during the latter stage, crosslinking takes the predominant place and the tensile strength increases slightly. HALS and UVA have a little effect on the maintaining of elongation at break of PVC/NBR blends. POLYM. ENG. SCI., 2013. © 2013 Society of Plastics Engineers
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