Patrícia
Pereira
a,
Phillip E.
Savage
*a and
Christian W.
Pester
*ab
aDepartment of Chemical Engineering, The Pennsylvania State University, University Park, PA 16802, USA. E-mail: psavage@psu.edu; pester@psu.edu
bDepartment of Chemistry and Department of Materials Science and Engineering, The Pennsylvania State University, University Park, Pennsylvania 16802, USA
First published on 27th January 2025
Correction for ‘Acid catalyst screening for hydrolysis of post-consumer PET waste and exploration of acidolysis’ by Patrícia Pereira et al., Green Chem., 2024, 26, 1964–1974, https://doi.org/10.1039/D3GC03906D.
The reaction temperature used to generate the data in Fig. 6 of the published paper was not 200 °C, as was reported. The authors have not been able to verify definitively the reaction temperature used, so they conducted a new set of polyethylene terephthalate (PET) depolymerization experiments in acetic acid and in propanoic acid. The yields of terephthalic acid (TPA) at 200 °C were always less than 3% in these new experiments. Experiments at 230 °C provided the yields in the figure below. The figure and associated caption shown below should replace Fig. 6 in the published article.
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Fig. 6 Effect of PET/HOAc or propanoic acid ratio on TPA yield from PET acidolysis (230 °C, 2 h, 0.2 gPET). |
Several sentences in the published article require updating in consideration of the new reaction temperature and TPA yields.
In the second paragraph in section 3.3, “YTPA was above 80% at low PET/acetic acid ratios, but it decreased to almost zero as the ratio increased.” should now read “YTPA was above 80% at low PET/acetic acid ratios, but it decreased to about 30% as the ratio increased.” In addition, the sentence “Similar to acetic acid, the TPA yield with propanoic acid decreased from a high of 71 ± 13% at 0.1 gPET gacid−1 to 34 ± 4% at 0.48 gPET gacid−1.” has been changed to “Similar to acetic acid, the TPA yield with propanoic acid decreased as the PET/acetic acid ratio increased.”
The entry in Table 1 for acetolysis has been updated, as shown below. Instead of 200 °C, the temperature should be 230 °C. The environmental energy impact value in the final column has been updated from 3.1 to 2.5.
Ref. | Reaction | Catalyst | Temp (°C) | Time (min) | gPET gsolvent−1 | ξ 104 (°C min) |
---|---|---|---|---|---|---|
a Additional solvent [Bmim]Cl/water. | ||||||
Below PET melting temperature | ||||||
This study | Hydrolysis | None | 200 | 120 | 0.1 | 587 |
Hydrolysis | Nitric acid, pH = 1.4 | 200 | 120 | 0.1 | 8.5 | |
Hydrolysis | TPA, 0.005 molTPA gPET−1 | 200 | 180 | 0.1 | 4.5 | |
Hydrolysis | 4-FBA, 0.01 mol4-FBA gPET−1 | 200 | 120 | 0.1 | 10.2 | |
Hydrolysis | Benzoic acid, 0.07 molBA gPET−1 | 200 | 120 | 0.1 | 7.0 | |
Hydrolysis | Acetic acid, 0.17 molAA gPET−1 | 200 | 120 | 0.1 | 4.4 | |
Hydrolysis | ZnI2, pH = 5.0 | 200 | 120 | 0.1 | 4.0 | |
Acetolysis | None | 230 | 120 | 0.2 | 2.5 | |
Yang et al.25 | Hydrolysis | PTSA, 16 gcatalyst gPET−1 | 150 | 90 | 0.05 | 6.1 |
Liu et al.22 | Hydrolysis | [HSO3-pmin][HSO4]a 1/5 gcatalyst gPET−1 | 170 | 270 | 0.75 | 2.4 |
W. Yang et al.7 | Hydrolysis | TPA, 0.005 molTPA gPET−1 | 220 | 180 | 0.125 | 5.6 |
Above PET melting temperature | ||||||
This study | Hydrolysis | None | 270 | 30 | 0.1 | 5.7 |
Hydrolysis | HY | 270 | 30 | 0.1 | 1.3 | |
Peng et al.26 | Acetolysis | None | 280 | 120 | 0.2 | 2.4 |
In the second paragraph of section 3.4, “The use of acetic acid as a solvent (with no catalyst) led to a value of ξ = 3.1 × 104 °C min from acetolysis at 200 °C.” should now read “The use of acetic acid as a solvent (with no catalyst) led to a value of ξ = 2.5 × 104 °C min from acetolysis at 230 °C.”
In the fifth paragraph of the Conclusions, “The present preliminary examination of acidolysis of PET showed that TPA yields of over 80% can be achieved at 200 °C from solid PET.” has been changed to “The present preliminary examination of acidolysis of PET showed that TPA yields of over 80% can be achieved at 230 °C from solid PET.”
The authors declare that neither the new data nor the updated text affects the primary conclusion from this portion of the article: acidolysis using acetic acid and propanoic acid shows promising results that merit further exploration.
The Royal Society of Chemistry apologises for these errors and any consequent inconvenience to authors and readers.
This journal is © The Royal Society of Chemistry 2025 |