Andrea Polachova, Jaroslav Cisar, Martin Novak, Miroslava Dusankova, Vladimir Sedlarik
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引用次数: 0
Abstract
This study investigates the effects of repeated reprocessing on polypropylene (PP) and the associated release of low-molecular-weight substances into liquid and gaseous phases. Specifically, virgin polypropylene (Mosten TB 003) was mechanically reprocessed 1, 5, 10, 15, and 18 times to simulate its participation in the mechanical recycling cycle. The mechanical properties of all PP samples were evaluated, along with their potential migration into water. The stability of PP was assessed using differential scanning calorimetry (DSC), while molecular weight distribution was determined via high-temperature gel permeation chromatography (GPC) with refractometric and viscosimetric detection. GPC and DSC analyses of PP's mechanical properties revealed that reprocessing led to chain shortening and reduced thermal stability, evidenced by material yellowing. For PP recycled 18 times—representing the maximum feasible number of reprocessing cycles—the molecular weight decreased by approximately 30 % compared to virgin PP. The potential release of volatile substances (odorants) into the environment during PP processing was monitored using headspace solid-phase microextraction (HS-SPME) combined with gas chromatography-mass spectrometry (GC–MS). Two extraction temperatures were examined: 90 °C, simulating the maximum temperature PP reaches indoors, and 120 °C, representing outdoor conditions. The least volatile substances were detected in the most extensively reprocessed PP (18x). At 120 °C, the most significant compounds identified included phenolic substances such as 2,4-di‑tert-butylphenol, 2,6-di‑tert‑butyl‑p-benzoquinone, 4-hydroxybenzaldehyde, estragole, and 2-phenoxyethanol. The number of reprocessing cycles was indicated by the presence of 4-methyl-1,6-heptadien-4-ol.
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.