2023
DOI: 10.1016/j.jhazmat.2023.131801
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Melt polycondensation of poly (butylene oxalate-co-succinate) with great potential in curbing marine plastic pollution

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Cited by 12 publications
(6 citation statements)
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“…The 1 H NMR spectra of PESS30, PESS50, and PESS70 before and after degradation are shown in Figure . For PESS30, the Φ SS calculated by integrating the protons g and a ( Φ SS = 2 I g / I a ) increased from 31.3% to 68.0% then decreased to 62.5%, as the main degradation was the ES segment Figure b depicts the 1 H NMR spectra of PESS50 before and after degradation, revealing a similar pattern to that of PESS30.…”
Section: Resultsmentioning
confidence: 73%
See 1 more Smart Citation
“…The 1 H NMR spectra of PESS30, PESS50, and PESS70 before and after degradation are shown in Figure . For PESS30, the Φ SS calculated by integrating the protons g and a ( Φ SS = 2 I g / I a ) increased from 31.3% to 68.0% then decreased to 62.5%, as the main degradation was the ES segment Figure b depicts the 1 H NMR spectra of PESS50 before and after degradation, revealing a similar pattern to that of PESS30.…”
Section: Resultsmentioning
confidence: 73%
“…For PESS30, the Φ SS calculated by integrating the protons g and a (Φ SS = 2I g /I a ) increased from 31.3% to 68.0% then decreased to 62.5%, as the main degradation was the ES segment. 46 Figure 9b depicts the 1 H NMR spectra of PESS50 before and after degradation, revealing a similar pattern to that of PESS30. However, the growth of SS chain segments after acid treatment was smaller than that of PESS30, indicating that the higher spiroglycol unit content was incorporated into the copolyester, and the more acidic degradation was triggered by the acidic environment.…”
Section: ■ Introductionmentioning
confidence: 69%
“…The oxalate group has higher reactivity compared with common ester groups, which can be attributed to the strong electrophilicity caused by the electron-withdrawing effect of the neighbouring carbonyl groups. 9 The reactivity of n -alkyl diols also increased with the increase of carbon chain length. 7,16–18 This inspired us to explore catalyst-free preparation of HWM PAOs.…”
Section: Introductionmentioning
confidence: 99%
“…Wei et al used 0.12 mol% tetrabutyl titanate (TBT) as the catalyst to give yellow PAOs in 8 h with weight-average molecular weights ( M w ) of 40–80 kDa. 7 Miller et al used para -toluene sulfonic acid ( p -TSA) as the catalyst at 2 mol% to prepare PAOs ( M w = 33–71 kDa) in 6 h. 8 Wang and Hu et al adopted antimony oxide as the catalyst to obtain pale yellow poly(butylene oxalate) ( M w ∼ 75 kDa) in 15–22 h. 9 The high loading of metal catalysts is beneficial to shorten the reaction time. Nonetheless, the drawback of catalyst-related discoloration of the products is difficult to avoid, particularly when high-efficiency metal catalysts are used.…”
Section: Introductionmentioning
confidence: 99%
“…The introduction of polyether blocks to synthesize PBS copolyesters could enhance the impact strength. However, the researchers have found that polyether reduces the tensile strength, flexural strength, thermal stability, and hydrolyzing resistance of PBS copolyesters. , To overcome the above defects, there is an urgent need to choose appropriate monomers to enhance the mechanical properties, thermal stability, and hydrophilicity of PBS.…”
Section: Introductionmentioning
confidence: 99%