Have a personal or library account? Click to login
Photophysical Investigations of the Organic Compounds Synthesised from Waste Poly(Ethylene Terephthalate) Cover

Photophysical Investigations of the Organic Compounds Synthesised from Waste Poly(Ethylene Terephthalate)

Open Access
|Jul 2024

References

  1. Nistico R. Polyethylene terephthalate (PET) in the packaging industry. Polymer Testing. 2020;90:106707. DOI: 10.1016/j.polymertesting.2020.106707.
  2. Chen S, Xie S, Guang S, Bao J, Zhang X, Chen W. Crystallization and thermal behaviors of poly(ethylene terephthalate)/bisphenols complexes through melt post-polycondensation. Polymers. 2020;12:3053. DOI: 10.3390/polym12123053.
  3. Suhaimi NAS, Muhamad F, Razak NAA, Zeimaran E. Recycling of polyethylene teraphthalate wastes: A review of technologies, routes, and applications. Polymer Eng Sci. 2022:1-21. DOI: 10.1002/pen.26017.
  4. Barber NA. Polyethylene Teraphthalate Uses, Properties and Degradation. New York: Nova Science Publishers, Inc; 2017. ISBN: 9781536119916.
  5. Qian K, Kumar A. Recent advances in utilization of biochar. Renew Sust Energy Rev. 2015;42:1055-64. DOI: 10.1016/j.rser.2014.10.074.
  6. Rabek JF. Polimery i ich zastosowanie interdyscyplinarne (Polymers and their interdisciplinary applications). Warszawa: Wydawnictwo Naukowe PWN; 2020. ISBN: 9788301210007.
  7. Saebea D, Ruengrit P, Arpornwichanop A, Patcharavorachot Y. Gasification of plastic waste for synthesis gas production. Energy Reports. 2020;6:202-07. DOI: 10.1016/j.egyr.2019.08.043.
  8. Soong YHV, Sobkowicz MJ, Xie D. Recent advances in biological recycling of polyethylene. Bioengineering. 2022;9:1-27. DOI: 10.3390/bioengineering9030098.
  9. Dissanayake L, Jayakody LN. Engineering microbes to bio-upcycle polyethylene terephthalate. Front Bioeng Biotechnol. 2021;2:656465. DOI: 10.3389/fbioe.2021.656465.
  10. Sabu T, Kanny K, Thomas MG, Rane A, Abitha VK. Recycling of Polyethylene Terephthalate Bottles. New York: Elsevier Inc; 2018. ISBN: 9780128113615. DOI: 10.1016/C2016-0-01084-7.
  11. Yue H, Zhao Y, Ma X, Gong J. Ethyleneglycol: properties, synthesis, and applications. Chem Soc Rev. 2012;41:4218-44. DOI: 10.1039/C2CS15359A.
  12. Larocca JP, Sharkawi MAY. Synthesis of some substituted amides of terephthalic and isophthalic acids. J Pharmaceutical Sci. 1967;56:916-8. DOI: 10.1002/jps.2600560732.
  13. Sellarajah S, Lekishvili T, Bowring C, Thompsett AR, Rudyk H, Birket ChR, et al. Synthesis of analogues of congo red and evaluation of their anti-prion activity. J Med Chem. 2004;47:5515-34. DOI:10.1021/jm049922t.
  14. Kurandina D, Huang B, Xu W, Hanikiel N, Daru A, Stroscio GD, et al. A porous crystalline nitrone-linked covalent organic framework. Communications. 2023;62:202307674. DOI: 10.1002/anie.202307674.
  15. Wang XL, Mu B, Lin HY, Yang S, Liu GCh. Two novel 3D copper(II) complex based on a rigid bis-pyridyl-bis-amide and two polycarboxylates mixed ligands: assembly, structures and properties. J Mol Structure. 2013;1036:380-5. DOI: 10.1016/j.molstruc.2012.12.001.
  16. Cheng H, Shang M, He Y, Shentu B, Gao Z. Synthesis and effect on N,N’-diphenylterephthalamide on crystallization of isotactic polypropylene. Polymer Sci. 2020;62:473-82. DOI: 10.1134/S1560090420050036.
  17. Kotowicz S, Korzec M, Siwy M, Golba S, Małecki JG, Janeczek H, et al. Novel 1,8-naphthalimides substituted at 3-C position: Synthesis and evaluation of thermal, electrochemical and luminescent properties. Dyes Pig. 2018;158:65-78. DOI: 10.1016/j.dyepig.2018.05.017.
  18. Bujak P, Kulszewicz-Bajer I, Zagorska M, Maurel V, Wielgus I, Proń A. Polymers for electronics and spintronics. Chem Soc Rev. 2013;42:8895-999. DOI: 10.1039/C3CS60257E.
  19. Pezz N, Janiska MCh, Imhof W. The first application of quantitative 1H NMR spectroscopy as a simple and fast method of identification and quantification of microplastic particles (PE, PET and PS). Anal Bio Chem. 2018;411:823-33. DOI: 10.1007/s00216-018-1510-z.
  20. Dian HL, Meng FL, Yang ChX, Yan XP. Irreverible amide-linked covalent organic framework for selective and ultrafast gold recovery. Angew Chemie. 2020;59:17607-13. DOI: 10.1002/a.nie.202006535.
  21. Ackermann SM, Lachenmeier DW, Kuballa T, Schutz B, Spraul M, Bunzel M. NMR-based differentiation of conventionally from organically produced chicken eggs in Germany. Magn Reson Chem. 2019;57:579-88. DOI: 10.1002/mrc.3920143.
  22. Wilsens CHRM, Deshmukh YS, Noordover BAJ, Rastogi S. Influence of the 2,5-furandicarboxamide moiety on hydrogen bonding in aliphatic-aromatic poly(ester amide)s. Macromolecules. 2014;47:6196-206. DOI: 10.1021/ma501310f.
  23. Lima JC, Costa ARM, Sousa JC, Arruda SA, Almeida YMB. Thermal behavior of polyethylene terephthalate/organoclay nanocomposites: investigating copolymers as metrices. Polymer Composites. 2021;42:849-64. DOI: 10.1002/pc.25870.
  24. Cheng N, Yan Q, Liu S, Zhao D. Probing the intermolecular interactions of aromatic amides containing N-heterocycles and triptycene. CrystEngComm. 2014;16:4265-73. DOI: 10.1039/C4CE00089G.
  25. Kotowicz S, Korzec M, Pająk AK, Golba S, Małecki JG, Siwy M, et al. New acceptor-donor-acceptor systems based on bis-(imino-1,8-naphthalimide). Materials. 2021;14:2714-32. DOI: 10.3390/ma14112714.
  26. Espinoza EM, Clark JA, Derr JB, Bao D, Georgieva B, Quina FH, et al. How do amides affect the electronic properties of pyrene? ACS Omega. 2018;3:12857-67. DOI: 10.1021/acsomega.8b01581.
  27. Alonso-Navarro MJ, Harbuzaru A, Martinez-Fernandez M, Camero PP, Navarrere JTL, Ramos MM, et al. Synthesis and electronic properties of nitrogen-doped π-extended polycyclic aromatic dicarboximides with multiple redox processes. J Mater Chem C. 2021;9:7936-49. DOI: 10.1039/D1TC01239H.
  28. Amin MF, Gnida P, Kotowicz S, Małecki JG, Siwy M, Nitschke P, et al. Spectroscopic and physicochemical investigations of azomethines with triphenylamine core towards optoelectronics. Materials. 2022;15:7197-214. DOI: 10.3390/ma15207197.
  29. Kaim A, Piotrowski P, Zarębska K, Bogdanowicz KA, Przybył W, Kwak A, et al. Thermal imaging and deep optical and electrochemical study of C70 fullerene derivatives with thiophene, pyrrolidine or indene moieties along with electropolymerization with thiophene substituted imine: Blends with P3HT and PTB7. Electrochim Acta. 2022;426:140741. DOI: 10.1016/j.electacta.2022.140741.
DOI: https://doi.org/10.2478/eces-2024-0018 | Journal eISSN: 2084-4549 | Journal ISSN: 1898-6196
Language: English
Page range: 253 - 266
Published on: Jul 10, 2024
In partnership with: Paradigm Publishing Services
Publication frequency: 4 issues per year

© 2024 Sonia Kotowicz, Mateusz Korzec, Maciej Kapkowski, Agnieszka Katarzyna Pająk, published by Society of Ecological Chemistry and Engineering
This work is licensed under the Creative Commons Attribution-NonCommercial-NoDerivatives 3.0 License.