2015
DOI: 10.1039/c5gc01048a
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Chemical recycling of unsaturated polyester resin and its composites via selective cleavage of the ester bond

Abstract: Unsaturated polyester resin (UPR) is recycled by using the AlCl3/CH3COOH degradation system via selectively cleaving the ester bond.

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Cited by 86 publications
(24 citation statements)
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“…The recent development of novel polymers with dynamic exchange reaction (ER) enables thermosets dissolution under mild conditions. [6][7][8][9][10][11][12] The dynamic bonds activated by a specic stimulus or chemicals lead to network rearrangement and selective bond cleavage. [13][14][15][16] These dynamic polymers have the desirable attributes of conventional thermosets, but also have more attractive attributes, such as self-healing and reprocessing of thermosets.…”
Section: Introductionmentioning
confidence: 99%
“…The recent development of novel polymers with dynamic exchange reaction (ER) enables thermosets dissolution under mild conditions. [6][7][8][9][10][11][12] The dynamic bonds activated by a specic stimulus or chemicals lead to network rearrangement and selective bond cleavage. [13][14][15][16] These dynamic polymers have the desirable attributes of conventional thermosets, but also have more attractive attributes, such as self-healing and reprocessing of thermosets.…”
Section: Introductionmentioning
confidence: 99%
“…Increased awareness of environmental impact from plastics has intensied the research into bio-based and recyclable polymeric materials. [1][2][3][4] A class of plastics showing strong potential is polyesters. Polyesters are challenged in high-temperature environments due to their vulnerability to thermally induced mechanical changes which limits service life.…”
Section: Introductionmentioning
confidence: 99%
“…The chemical recovery of anhydride‐cured epoxy thermosets typically included organic solvolysis and hydrolysis [28–40] . Due to the lipophilic wettability of epoxy thermosets, it is more efficient to perform degradation in organic solvents, mostly alcohols, with the assistance of catalysts, such as zinc acetate, 1,5,7‐Triazabicyclo[4.4.0]dec‐5‐ene (TBD), and others [33–38] .…”
Section: Introductionmentioning
confidence: 99%
“…On the one hand, it makes the hydrolysis product easily separated from the aqueous system due to its insolubility; on the other hand, it makes the hydrolysis process more difficult due to nonwettability of the epoxy thermoset to the aqueous reactants. Therefore, harsh conditions, such as higher temperature (190–220 °C) and longer time (5–9 h) are always required [29–31] …”
Section: Introductionmentioning
confidence: 99%