This article is about the plastic. For the Radiohead song, see Polyethylene (Parts 1 & 2).
"Polythene" redirects here. For the Feeder album, see Polythene (album).
This article's lead section may be too short to adequately summarize the key points. Please consider expanding the lead to provide an accessible overview of all important aspects of the article.(July 2023)
Polyethylene
Names
IUPAC name
Polyethene or poly(methylene)[1]
Other names
Polyethylene Polythene
Identifiers
CAS Number
9002-88-4Y
Abbreviations
PE
ChemSpider
none
ECHA InfoCard
100.121.698
KEGG
C19503Y
MeSH
Polyethylene
PubChem CID
6325
UNII
3W404QE89SY
CompTox Dashboard (EPA)
DTXSID8031946
Properties
Chemical formula
(C2H4)n
Density
0.88–0.96 g/cm3[2]
Melting point
115–135 °C (239–275 °F; 388–408 K)[2]
Solubility in water
Not soluble
log P
1.02620[3]
Magnetic susceptibility (χ)
−9.67×10−6 (HDPE, SI, 22 °C)[4]
Thermochemistry
Std enthalpy of formation (ΔfH⦵298)
−28 to −29 kJ/mole[5]
Heat of combustion, higher value (HHV)
650-651 kJ/mole, 46 MJ/kg[5]
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Infobox references
Chemical compound
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Polyethylene or polythene (abbreviated PE; IUPAC name polyethene or poly(methylene)) is the most commonly produced plastic.[7] It is a polymer, primarily used for packaging (plastic bags, plastic films, geomembranes and containers including bottles, etc.). As of 2017[update], over 100 million tonnes of polyethylene resins are being produced annually, accounting for 34% of the total plastics market.[8][9]
Many kinds of polyethylene are known, with most having the chemical formula (C2H4)n. PE is usually a mixture of similar polymers of ethylene, with various values of n. It can be low-density or high-density and many variations thereof. Its properties can be modified further by crosslinking or copolymerization. All forms are nontoxic as well as chemically resilient, contributing to polyethylene‘s popularity as a multi-use plastic. However, polyethylene‘s chemical resilience also makes it a long-lived and decomposition-resistant pollutant when disposed of improperly.[10] Being a hydrocarbon, polyethylene is colorless to opaque (without impurities or colorants) and combustible.[11]
^Compendium of Polymer Terminology and Nomenclature – IUPAC Recommendations 2008(PDF). Retrieved 28 August 2018.
^ abBatra, Kamal (2014). Role of Additives in Linear Low Density Polyethylene (LLDPE) Films. p. 9. Retrieved 16 September 2014.
^"poly(ethylene)". ChemSrc.
^Wapler, M. C.; Leupold, J.; Dragonu, I.; von Elverfeldt, D.; Zaitsev, M.; Wallrabe, U. (2014). "Magnetic properties of materials for MR engineering, micro-MR and beyond". JMR. 242: 233–242. arXiv:1403.4760. Bibcode:2014JMagR.242..233W. doi:10.1016/j.jmr.2014.02.005. PMID 24705364. S2CID 11545416.
^ abPaul L. Splitstone and Walter H. Johnson (20 May 1974). "The Enthalpies of Combustion and Formation of Linear Polyethylene" (PDF). Journal of Research of the National Bureau Af Standards.
^Hemakumara, G. P. T. S.; Madhusankha, T. G. Shamal (2023). "Challenges of Reducing Polythene and Plastic in Sri Lanka: A Case Study of Attanagalla Secretariat Division". Socially Responsible Plastic. Developments in Corporate Governance and Responsibility. 19: 59–73. doi:10.1108/S2043-052320230000019004. ISBN 978-1-80455-987-1.
^Cite error: The named reference Ullmann was invoked but never defined (see the help page).
^Geyer, Roland; Jambeck, Jenna R.; Law, Kara Lavender (1 July 2017). "Production, use, and fate of all plastics ever made". Science Advances. 3 (7): e1700782. Bibcode:2017SciA....3E0782G. doi:10.1126/sciadv.1700782. PMC 5517107. PMID 28776036.
^"Plastics: The Facts" (PDF). Plastics Europe. Archived from the original (PDF) on 4 February 2018. Retrieved 29 August 2018.
^Yao, Zhuang; Jeong Seong, Hyeon; Jang, Yu-Sin (2022). "Environmental toxicity and decomposition of polyethylene". ScienceDirect: 1, 3. Retrieved 25 April 2024.
^Sepe, Michael. "Understanding the 'Science' of Color". Plastics Technology. Retrieved 25 April 2024.
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