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End‐of‐Life Treatment of Poly(Vinyl Chloride) and Chlorinated Polyethylene by Dehydrochlorination in Ionic Liquids
Author(s) -
Glas Daan,
Hulsbosch Joris,
Dubois Philippe,
Binnemans Koen,
De Vos Dirk E.
Publication year - 2014
Publication title -
chemsuschem
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.412
H-Index - 157
eISSN - 1864-564X
pISSN - 1864-5631
DOI - 10.1002/cssc.201300970
Subject(s) - vinyl chloride , depolymerization , polymer , polyethylene , ionic liquid , chemistry , chloride , catalysis , polyvinyl chloride , polymer chemistry , chemical engineering , organic chemistry , copolymer , engineering
There is an urgent need for green technologies to remove halogens from halogenated polymers at the end of their lifetime. Ionic liquids (ILs) were used to dehydrochlorinate and/or dissolve the chlorinated polymers poly(vinyl chloride) (PVC) and chlorinated polyethylene (CPE). The dehydrochlorination activity of an IL depends mainly on its anion and is related to the high hydrogen‐bond‐accepting ability ( β value) of the anion. Different phosphonium ILs successfully dissolve and dehydrochlorinate PVC and CPE at temperatures from 80 °C. PVC is dehydrochlorinated up to 98 % after 60 min in tetrabutylphosphonium chloride ([P 4444 ][Cl]) at 180 °C. PVC pieces stabilized by calcium stearate (4 mm 3 ) are dehydrochlorinated more slowly; conversions of 85 and 96 % are reached after 1 and 8 h, respectively. Smaller pieces are dehydrochlorinated faster. High loadings, for example, 0.3 g stabilized PVC in 0.5 g IL, can be applied with only a minor loss of conversion. [P 4444 ][Cl] proved to be stable during several consecutive reactions; after each run more than 99 % of the IL can be recovered. The structure of the dehydrochlorinated PVC was studied by 13 C cross‐polarization magic‐angle spinning NMR and FTIR spectroscopy; the removal of Cl and the formation of double bonds were confirmed. Carefully dehydrochlorinated CPE was processed further by acyclic diene metathesis depolymerization with ethylene and the Hoveyda–Grubbs second‐generation catalyst to yield α,ω‐dienes such as 1,5‐hexadiene and 1,6‐heptadiene.