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 in | Journal of applied polymer science Vol. 91; no. 3; pp. 1525 - 1537 |
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Main Authors | , , |
Format | Journal Article |
Language | English |
Published |
Hoboken
Wiley Subscription Services, Inc., A Wiley Company
05.02.2004
Wiley |
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Online Access | Get full text |
ISSN | 0021-8995 1097-4628 1097-4628 |
DOI | 10.1002/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 |
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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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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. – reference: Barabas, K.; Iring, M.; Kelen, T.; Tüdos, F. J Polym Sci 1976, 57, 65-71. – reference: Holmström, A.; Sörvik, E. J Chromat 1970, 53, 95-108. – reference: Hoff, A.; Jacobsson, S. J Appl Polym Sci 1981, 26, 3409-3423. – volume: 86 start-page: 1580 year: 2002 end-page: 1586 publication-title: J Appl Polym Sci – volume: 82 year: 2000 publication-title: Paper Timber – volume: 61 start-page: 329 year: 1998 end-page: 342 publication-title: Polym Degrad Stabil – volume: 57 start-page: 313 issue: 3 year: 1997 end-page: 324 publication-title: Polym Degrad Stabil – volume: 63 start-page: 41 year: 1998 end-page: 52 publication-title: Polym Degrad Stabil – volume: 57 start-page: 65 year: 1976 end-page: 71 publication-title: J Polym Sci – volume: 26 start-page: 3409 year: 1981 end-page: 3423 publication-title: J Appl Polym Sci – start-page: 55 year: 1973 – volume: 14 start-page: 439 year: 1978 end-page: 442 publication-title: Eur Polym J – volume: 71 year: 2001 publication-title: Borealis, Low Density Polyethylenes for Extrusion Coating – volume: 53 start-page: 95 year: 1970 end-page: 108 publication-title: J Chromat – year: 1978 – volume: 56 start-page: 1 year: 1997 end-page: 9 publication-title: Polym Degrad Stabil – volume: 68 start-page: 337 issue: 3 year: 2000 end-page: 352 publication-title: Polym Degrad Stabil – year: 1990 – year: 1976 – volume: 67 start-page: 35 year: 2000 end-page: 47 publication-title: Polym Degrad Stabil – volume: 16 start-page: 2555 year: 1978 end-page: 2586 publication-title: J Polym Sci, Polym Chem Ed – ident: e_1_2_6_11_2 doi: 10.1520/DS48A-EB – ident: e_1_2_6_18_2 doi: 10.1016/S0141-3910(99)00115-9 – ident: e_1_2_6_19_2 – volume: 82 year: 2000 ident: e_1_2_6_2_2 publication-title: Paper Timber – ident: e_1_2_6_3_2 doi: 10.1002/polc.5070570108 – ident: e_1_2_6_15_2 doi: 10.1016/S0141-3910(96)00193-0 – ident: e_1_2_6_20_2 doi: 10.1002/pol.1978.170161012 – ident: e_1_2_6_17_2 doi: 10.1016/S0141-3910(00)00018-5 – ident: e_1_2_6_8_2 doi: 10.1016/S0021-9673(00)86708-4 – ident: e_1_2_6_7_2 doi: 10.1016/S0141-3910(97)00217-6 – start-page: 55 volume-title: Termisk och termooxidative nedbrytning av polyeten. studium av långkedjeförgreningsgradens och molekylviktsfördelningens inverkan hos LD‐polyeten, in Institutionen för organisk kemi Polymergruppen year: 1973 ident: e_1_2_6_4_2 – ident: e_1_2_6_13_2 doi: 10.1007/978-94-009-2163-4 – ident: e_1_2_6_14_2 doi: 10.1016/B978-0-08-091740-5.50014-4 – ident: e_1_2_6_5_2 doi: 10.1016/S0141-3910(98)00059-7 – ident: e_1_2_6_9_2 doi: 10.1002/app.1981.070261020 – ident: e_1_2_6_6_2 doi: 10.1016/0014-3057(78)90065-4 – volume-title: Rheology in Polymer Processing year: 1976 ident: e_1_2_6_12_2 – ident: e_1_2_6_16_2 doi: 10.1016/S0141-3910(97)00026-8 – ident: e_1_2_6_10_2 doi: 10.1002/app.11030 |
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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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