Degradation of polyethylene during extrusion. II. Degradation of low-density polyethylene, linear low-density polyethylene, and high-density polyethylene in film extrusion

The degradation of different polyethylenes—low‐density polyethylene (LDPE), linear low‐density polyethylene (LLDPE), and high‐density polyethylene (HDPE)—with and without antioxidants and at different oxygen concentrations in the polymer granulates, have been studied in extrusion coating processing....

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Published inJournal of applied polymer science Vol. 91; no. 3; pp. 1525 - 1537
Main Authors Andersson, Thorbjörn, Stålbom, Berit, Wesslén, Bengt
Format Journal Article
LanguageEnglish
Published Hoboken Wiley Subscription Services, Inc., A Wiley Company 05.02.2004
Wiley
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ISSN0021-8995
1097-4628
1097-4628
DOI10.1002/app.13024

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Abstract The degradation of different polyethylenes—low‐density polyethylene (LDPE), linear low‐density polyethylene (LLDPE), and high‐density polyethylene (HDPE)—with and without antioxidants and at different oxygen concentrations in the polymer granulates, have been studied in extrusion coating processing. The degradation was followed by online rheometry, size exclusion chromatography, surface oxidation index measurements, and gas chromatography–mass spectrometry. The degradations start in the extruder where primary radicals are formed, which are subject to the auto‐oxidation when oxygen is present. In the extruder, crosslinking or chain scissions reactions are dominating at low and high melt temperatures, respectively, for LDPE, and chain scission is overall dominating for the more linear LLDPE and HDPE resins. Additives such as antioxidants react with primary radicals formed in the melt. Degradation taking place in the film between the die orifice, and the quenching point is mainly related to the exposure time to air oxygen. Melt temperatures above 280°C give a dominating surface oxidation, which increases with the exposure time to air between die orifice and quenching too. A number of degradation products were identified—for example, aldehydes and organic acids—which were present in homologous series. The total amount of aldehydes and acids for each number of chain carbon atoms were appeared in the order of C5>C4>C6>C7≫C2 for LDPE, C5>C6>C4>C7≫C2 for LLDPE, and C5>C6>C7>C4≫C2 for HDPE. The total amounts of oxidized compounds presented in the films were related to the processing conditions. Polymer melts exposed to oxygen at the highest temperatures and longest times showed the presence dialdehydes, in addition to the aldehydes and acids. © 2003 Wiley Periodicals, Inc. J Appl Polym Sci 91: 1525–1537, 2004
AbstractList The degradation of different polyethylenes-low-density polyethylene (LDPE), linear low-density polyethylene (LLDPE), and high-density polyethylene (HDPE)-with and without antioxidants and at different oxygen concentrations in the polymer granulates, have been studied in extrusion coating processing. The degradation was followed by online rheometry, size exclusion chromatography, surface oxidation index measurements, and gas chromatography-mass spectrometry. The degradations start in the extruder where primary radicals are formed, which are subject to the auto-oxidation when oxygen is present. In the extruder, crosslinking or chain scissions reactions are dominating at low and high melt temperatures, respectively, for LDPE, and chain scission is overall dominating for the more linear LLDPE and HDPE resins. Additives such as antioxidants react with primary radicals formed in the melt. Degradation taking place in the film between the die orifice, and the quenching point is mainly related to the exposure time to air oxygen. Melt temperatures above 280degreesC give a dominating surface oxidation, which increases with the exposure time to air between die orifice and quenching too. A number of degradation products were identified-for example, alclehydes and organic acids-which were present in homologous series. The total amount of aldehydes and acids for each number of chain carbon atoms were appeared in the order of C5>C4>C6>C7much greater thanC2 for LDPE, C5>C6>C4> C7much greater thanC2 for LLDPE, and C5>C6>C7>C4much greater thanC2 for HDPE. The total amounts of oxidized compounds presented in the films were related to the processing conditions. Polymer melts exposed to oxygen at the highest temperatures and longest times showed the presence dialdehydes, in addition to the aldehydes and acids. (C) 2003 Wiley Periodicals, Inc. J Appl Polyrn Sci 91: 1525-1537, 2004.
The degradation of different polyethylenes—low‐density polyethylene (LDPE), linear low‐density polyethylene (LLDPE), and high‐density polyethylene (HDPE)—with and without antioxidants and at different oxygen concentrations in the polymer granulates, have been studied in extrusion coating processing. The degradation was followed by online rheometry, size exclusion chromatography, surface oxidation index measurements, and gas chromatography–mass spectrometry. The degradations start in the extruder where primary radicals are formed, which are subject to the auto‐oxidation when oxygen is present. In the extruder, crosslinking or chain scissions reactions are dominating at low and high melt temperatures, respectively, for LDPE, and chain scission is overall dominating for the more linear LLDPE and HDPE resins. Additives such as antioxidants react with primary radicals formed in the melt. Degradation taking place in the film between the die orifice, and the quenching point is mainly related to the exposure time to air oxygen. Melt temperatures above 280°C give a dominating surface oxidation, which increases with the exposure time to air between die orifice and quenching too. A number of degradation products were identified—for example, aldehydes and organic acids—which were present in homologous series. The total amount of aldehydes and acids for each number of chain carbon atoms were appeared in the order of C5>C4>C6>C7≫C2 for LDPE, C5>C6>C4>C7≫C2 for LLDPE, and C5>C6>C7>C4≫C2 for HDPE. The total amounts of oxidized compounds presented in the films were related to the processing conditions. Polymer melts exposed to oxygen at the highest temperatures and longest times showed the presence dialdehydes, in addition to the aldehydes and acids. © 2003 Wiley Periodicals, Inc. J Appl Polym Sci 91: 1525–1537, 2004
Author Andersson, Thorbjörn
Stålbom, Berit
Wesslén, Bengt
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Issue 3
Keywords Additive
Polyethylene
Low density ethylene polymer
Coating material
Molten state
High density ethylene polymer
Polymer
Crosslinking
Antioxidant
Linear low density ethylene polymer
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References_xml – reference: Holmström, A.; Sörvik, E. M. J Polym Sci, Polym Chem Ed 1978, 16, 2555-2586.
– reference: Borealis, Low Density Polyethylenes for Extrusion Coating, 2001, 71.
– reference: Gugumus, F. Polym Degrad Stabil 2000, 67, 35-47.
– reference: Gugumus, F. Polym Degrad Stabil 1998, 63, 41-52.
– reference: Khabbaz, F.; Albertsson, A.-C.; Karlsson, S. Polym Degrad Stabil 1998, 61, 329-342.
– reference: Boström, M. Termisk och termooxidative nedbrytning av polyeten. studium av långkedjeförgreningsgradens och molekylviktsfördelningens inverkan hos LD-polyeten, in Institutionen för organisk kemi Polymergruppen; Chalmers Tekniska Högskola: Göteborg, 1973; p 55.
– reference: Gugumus, F. Polym Degrad Stabil 2000, 68(3), 337-352.
– reference: Han, C. h. D. Rheology in Polymer Processing; Academic Press: New York, 1976.
– reference: Iring, M.; Laszlo-Hedvig, S.; Barabas, K.; Kelen, T.; Tüdos, F. Eur Polym J 1978, 14, 439-442.
– reference: Fazzalari, F. A. Compilation of Odor and Taste Threshold Values Data; American Society for Testing and Materials; Philadalphia, PA, 1978.
– reference: Andersson, T.; Wesslén, B.; Sandström, J. J Appl Polym Sci 2002, 86, 1580-1586.
– reference: Wiik, K.; Helle, T.; Paper Timber 2000, 82.
– reference: Bikiaris, D.; Prinos, J.; Perrier, C.; Panayiotou, C. Polym Degrad Stabil 1997, 57(3), 313-324.
– reference: Dealy, J. M.; Wissbrun, K. F. Melt Rheology and its Role in Plastics Processing; Library of Congress Cataloguing-in-Publication Data, 1990.
– reference: Colthup, N. B.; Daly, L. H.; Wiberley, S. E. Introduction to Infrared and Raman Spectroscopy, 3rd ed.; Boston: Academic Press, 1990.
– reference: Bikiaris, D.; Pinos, J.; Panayiotou, C. Polym Degrad Stabil 1997, 56, 1-9.
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– reference: Holmström, A.; Sörvik, E. J Chromat 1970, 53, 95-108.
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Snippet The degradation of different polyethylenes—low‐density polyethylene (LDPE), linear low‐density polyethylene (LLDPE), and high‐density polyethylene (HDPE)—with...
The degradation of different polyethylenes-low-density polyethylene (LDPE), linear low-density polyethylene (LLDPE), and high-density polyethylene (HDPE)-with...
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SubjectTerms antioxidants
Applied sciences
Chemical Sciences
degradation products
Exact sciences and technology
extrusion
Kemi
Natural Sciences
Naturvetenskap
oxidation
Physicochemistry of polymers
polyethylene
Polymer industry, paints, wood
Technology of polymers
Title Degradation of polyethylene during extrusion. II. Degradation of low-density polyethylene, linear low-density polyethylene, and high-density polyethylene in film extrusion
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https://onlinelibrary.wiley.com/doi/abs/10.1002%2Fapp.13024
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