2001
DOI: 10.1002/1521-3935(20010401)202:7<1246::aid-macp1246>3.0.co;2-5
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Time Evolution of the Concentration Profiles of HALS Stabilizers and of the Corresponding Oxidation Forms across Poly(propylene) Plaques Irradiated with UV-Visible Light

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Cited by 17 publications
(11 citation statements)
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“…The higher nitroxide content in HPEC1 in the early stages of thermal treatment can be explained by the expected higher diffusion of oxygen, HAS, and 2.7 × 10 -10 cm 2 /sec in the temperature range 298-348 K, and much higher in PE (74 × 10 -10 cm 2 /sec) in a similar temperature range (328-353 K). [24][25][26] The lower nitroxide content in HPEC1 as the treatment time increased cannot be explained if the only difference between the two HPEC samples is the rate of diffusion of oxygen and the mobility of other reactants. The explanation we offer is a higher consumption of nitroxides due to a higher degradation rate in HPEC1, as compared to HPEC2.…”
Section: Effect Of Stressmentioning
confidence: 99%
“…The higher nitroxide content in HPEC1 in the early stages of thermal treatment can be explained by the expected higher diffusion of oxygen, HAS, and 2.7 × 10 -10 cm 2 /sec in the temperature range 298-348 K, and much higher in PE (74 × 10 -10 cm 2 /sec) in a similar temperature range (328-353 K). [24][25][26] The lower nitroxide content in HPEC1 as the treatment time increased cannot be explained if the only difference between the two HPEC samples is the rate of diffusion of oxygen and the mobility of other reactants. The explanation we offer is a higher consumption of nitroxides due to a higher degradation rate in HPEC1, as compared to HPEC2.…”
Section: Effect Of Stressmentioning
confidence: 99%
“…The different radical profile found in the pigmented and not-pigmented samples is related to the different rates of degradation since, when the degradation is fast compared to oxygen diffusion, [12] as in the not-pigmented samples, where the light is capable of crossing the whole plaque, the nitroxide formation is observed only in the proximity of the surfaces. [5,9] On the other hand, when the rate of degradation is slow as in thermally treated samples, a large nitroxide concentration is observed also in the inner part of the plaque. The different results obtained in our experiments with respect to those reported by Schlick and coworkers, [9] should be attributed to the different temperatures of the sample during the irradiation, 362 K and 318 K, respectively.…”
Section: Radical Distribution Inside the Polymermentioning
confidence: 99%
“…[5][6][7][8] The joined use of EPR and EPRI provides information not only on the nature of the radical present in a given sample and on its concentration in the bulk, but also on its distribution at various depths of the sample. These information may be very important both in clarifying the mechanism of polymer stabilization as well as in the technological search of better additives or of mixtures of additives exhibiting a synergetic protective action for polymers.…”
Section: Introductionmentioning
confidence: 99%
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“…They originated from hindered amines used as stabilizers. Lucarini et al carried out detailed studies on PP using 1D EPRI [23][24][25], Marek et al extended the work to polystyrene [26], while Schlick and collaborators used both 1D EPRI and 2D SSI to study the degradation of heterophasic system such as poly(acrylonitrile-butadiene-styrene) and propylene-ethylene copolymers [27,28], or very recently to measure diffusion coefficients of nitroxide radicals in propylene-ethylene copolymers [29] (for review on this topic see Refs. [30][31][32] by Schlick).…”
Section: Introductionmentioning
confidence: 99%