{"title":"Degradation of multicomponent phosphate-plasticized PVC under thermal aging at moderate temperature","authors":"Mathilde Larrieu , Nathalie Balcar , Gilles Barabant , Maroussia Duranton , Odile Fichet , Sophie Cantin","doi":"10.1016/j.polymdegradstab.2025.111339","DOIUrl":null,"url":null,"abstract":"<div><div>Given the limited literature on the aging of multicomponent phosphate-plasticized polyvinylchloride (p-PVC), studies are needed to better understand the degradation mechanisms of such materials. To this end, p-PVC was formulated with three plasticizers: 12.5 % phosphate plasticizer, 17.5 % Diisodecyl Phthalate (DIDP), and 1.8 % Epoxidized Soybean Oil (ESBO). An additional 2.5 wt % of pigment paste was also added to half of the samples. To mimic real environment in which such materials can be present, the p-PVC films underwent artificial aging through temperature cycling (48 h at 80 °C, 24 h at 25 °C, with a constant relative humidity of 65 %). Yellowing was observed as the dominant colour change, with the metallic stabilizer contributing to a greenish hue at the start of aging. The study of plasticizer migration demonstrated that mainly the phosphate plasticizer was lost from the samples over 300 days of aging, while the DIDP and ESBO contents remained largely stable. Thus, phosphate diffusion coefficient in PVC of 4–6 × 10<sup>–15</sup> m²/s has been measured, which has not yet been reported in the literature. Finally, the pigment showed no effect on dehydrochlorination nor plasticizer loss, but contributed to conceal the sample yellowing.</div></div>","PeriodicalId":406,"journal":{"name":"Polymer Degradation and Stability","volume":"238 ","pages":"Article 111339"},"PeriodicalIF":6.3000,"publicationDate":"2025-03-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Polymer Degradation and Stability","FirstCategoryId":"92","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0141391025001697","RegionNum":2,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"POLYMER SCIENCE","Score":null,"Total":0}
引用次数: 0
Abstract
Given the limited literature on the aging of multicomponent phosphate-plasticized polyvinylchloride (p-PVC), studies are needed to better understand the degradation mechanisms of such materials. To this end, p-PVC was formulated with three plasticizers: 12.5 % phosphate plasticizer, 17.5 % Diisodecyl Phthalate (DIDP), and 1.8 % Epoxidized Soybean Oil (ESBO). An additional 2.5 wt % of pigment paste was also added to half of the samples. To mimic real environment in which such materials can be present, the p-PVC films underwent artificial aging through temperature cycling (48 h at 80 °C, 24 h at 25 °C, with a constant relative humidity of 65 %). Yellowing was observed as the dominant colour change, with the metallic stabilizer contributing to a greenish hue at the start of aging. The study of plasticizer migration demonstrated that mainly the phosphate plasticizer was lost from the samples over 300 days of aging, while the DIDP and ESBO contents remained largely stable. Thus, phosphate diffusion coefficient in PVC of 4–6 × 10–15 m²/s has been measured, which has not yet been reported in the literature. Finally, the pigment showed no effect on dehydrochlorination nor plasticizer loss, but contributed to conceal the sample yellowing.
期刊介绍:
Polymer Degradation and Stability deals with the degradation reactions and their control which are a major preoccupation of practitioners of the many and diverse aspects of modern polymer technology.
Deteriorative reactions occur during processing, when polymers are subjected to heat, oxygen and mechanical stress, and during the useful life of the materials when oxygen and sunlight are the most important degradative agencies. In more specialised applications, degradation may be induced by high energy radiation, ozone, atmospheric pollutants, mechanical stress, biological action, hydrolysis and many other influences. The mechanisms of these reactions and stabilisation processes must be understood if the technology and application of polymers are to continue to advance. The reporting of investigations of this kind is therefore a major function of this journal.
However there are also new developments in polymer technology in which degradation processes find positive applications. For example, photodegradable plastics are now available, the recycling of polymeric products will become increasingly important, degradation and combustion studies are involved in the definition of the fire hazards which are associated with polymeric materials and the microelectronics industry is vitally dependent upon polymer degradation in the manufacture of its circuitry. Polymer properties may also be improved by processes like curing and grafting, the chemistry of which can be closely related to that which causes physical deterioration in other circumstances.