Sofia Treccani, Jenny Alongi, Paolo Ferruti, Elisabetta Ranucci
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引用次数: 0
Abstract
Arginine- (M-ARG), glycine- (M-GLY), serine‑ (M-SER), histidine- (M-HIS) and tyrosine/arginine- (M-TYR30-ARG70) derived polyamidoamines (PAAs) were studied as cotton photostabilizers. Cotton strips with a 6 wt. % PAA add-on were subjected to accelerated photoaging in a solar chamber under UVA–UVB exposure at 40 % relative humidity and 30–35 °C. Colorimetric analysis was conducted at 15-minute intervals during irradiation. Virgin cotton exhibited significantly more yellowing than PAA-treated fabrics, except for those treated with M-TYR30-ARG70. Scanning electron microscopy revealed slight surface erosion on untreated cotton (COT) fibers after prolonged UV exposure, whereas PAA-treated cotton (COT/PAA) showed uniform PAA coatings with only minor surface wrinkles and localized fractures. Colorimetric analysis enabled ranking the photostability of COT/PAA samples as follows: COT/M-ARG > COT/M-GLY > COT/M-SER > COT/M-HIS > COT > COT/M-TYR30-ARG70. These results demonstrate that all PAAs enhanced UV protection, except for M-TYR30-ARG70. Nuclear magnetic resonance analysis of PAA coatings extracted from photoaged cotton showed no detectable structural degradation. The results confirm that α-amino acid-derived PAAs effectively protect cotton from photoaging, although formulations containing UVB-absorbing residues exhibit increased susceptibility to irradiation. The effectiveness of PAAs was attributed to the radical scavenging activity of tert‑amine groups and the side-chain residues within their repeat units.
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.