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Journal articles on the topic 'Aromatic polyesters'

Author: Grafiati

Published: 4 June 2021

Last updated: 6 September 2023

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1

Deokar, Satish S., Makarand D. Joshi, Asiya M. Tamboli, et al. "Aromatic Polyesters Containing Ether and a Kinked Aromatic Amide Structure in the Main Chain: Synthesis and Characterisation." Coatings 12, no. 2 (2022): 181. http://dx.doi.org/10.3390/coatings12020181.

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A novel bisphenol containing preformed multiple ether and amide linkages, N, N′-Bis (4-hydroxyphenoxyphenylene) isophthalamide (IPCD), was prepared and analysed by spectroscopic methods. New aromatic polyesters were prepared by polycondensation of IPCD with 1, 3-benzene diacidchloride and/or 1, 4-benzene diacidchloride. These obtained polyesters were structurally analysed by infra-red spectroscopy, measurements of inherent viscosity, wide-angle X-ray diffraction patterns, and thermal techniques such as differential scanning calorimetry (DSC), thermogravimetric analysis (TGA), and solubility te

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2

Vasava, Dilipkumar V., and Saurabh K. Patel. "Synthesis, Characterization and Study of Thermally Stable Fluorescent Polyesters." International Letters of Chemistry, Physics and Astronomy 70 (September 2016): 48–62. http://dx.doi.org/10.18052/www.scipress.com/ilcpa.70.48.

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Abstract: Numerous polyesters containing heterocyclic ring have been synthesized by the polycondensation method. Ten Polyesters were synthesised having different aliphatic-aromatic diols in the chain having s-triazine ring as main moiety. The polyesters were synthesized by polycondensation of 6-(N-Piperidinyl)-2,4-bis-(7-Hydroxy-Coumarin-3-carbonyl Chloride)-1,3,5-triazine [PCTC] with aliphatic and aromatic diols. Dark brown, light brown, golden and maroon colour showed by novel synthesized polyesters. The solubility of synthesized polyesters was observed in different solvents. The viscosity w

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3

Vasava, Dilipkumar V., and Saurabh K. Patel. "Synthesis, Characterization and Study of Thermally Stable Fluorescent Polyesters." International Letters of Chemistry, Physics and Astronomy 70 (September 29, 2016): 48–62. http://dx.doi.org/10.56431/p-033o63.

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Abstract: Numerous polyesters containing heterocyclic ring have been synthesized by the polycondensation method. Ten Polyesters were synthesised having different aliphatic-aromatic diols in the chain having s-triazine ring as main moiety. The polyesters were synthesized by polycondensation of 6-(N-Piperidinyl)-2,4-bis-(7-Hydroxy-Coumarin-3-carbonyl Chloride)-1,3,5-triazine [PCTC] with aliphatic and aromatic diols. Dark brown, light brown, golden and maroon colour showed by novel synthesized polyesters. The solubility of synthesized polyesters was observed in different solvents. The viscosity w

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4

Walczak, Małgorzata, Jaromir B. Lechowicz, and Henryk Galina. "Hyperbranched Aromatic Polyesters." Macromolecular Symposia 256, no. 1 (2007): 112–19. http://dx.doi.org/10.1002/masy.200751013.

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5

Bazin, Alfred, Luc Avérous, and Eric Pollet. "Ferulic Acid as Building Block for the Lipase-Catalyzed Synthesis of Biobased Aromatic Polyesters." Polymers 13, no. 21 (2021): 3693. http://dx.doi.org/10.3390/polym13213693.

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Enzymatic synthesis of aromatic biobased polyesters is a recent and rapidly expanding research field. However, the direct lipase-catalyzed synthesis of polyesters from ferulic acid has not yet been reported. In this work, various ferulic-based monomers were considered for their capability to undergo CALB-catalyzed polymerization. After conversion into diesters of different lengths, the CALB-catalyzed polymerization of these monomers with 1,4-butanediol resulted in short oligomers with a DPn up to 5. Hydrogenation of the double bond resulted in monomers allowing obtaining polyesters of higher m

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6

Bazheva, R. Ch, A. M. Kharaev та A. Z. Bazhev. "Modified aromatic со-polyesters". Scientific Medical Bulletin 2, № 2 (2015): 52–60. http://dx.doi.org/10.17117/nm.2015.02.052.

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7

Austin, Harry P., Mark D. Allen, Bryon S. Donohoe, et al. "Characterization and engineering of a plastic-degrading aromatic polyesterase." Proceedings of the National Academy of Sciences 115, no. 19 (2018): E4350—E4357. http://dx.doi.org/10.1073/pnas.1718804115.

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Poly(ethylene terephthalate) (PET) is one of the most abundantly produced synthetic polymers and is accumulating in the environment at a staggering rate as discarded packaging and textiles. The properties that make PET so useful also endow it with an alarming resistance to biodegradation, likely lasting centuries in the environment. Our collective reliance on PET and other plastics means that this buildup will continue unless solutions are found. Recently, a newly discovered bacterium, Ideonella sakaiensis 201-F6, was shown to exhibit the rare ability to grow on PET as a major carbon and energ

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8

Leitão, Ana Lúcia, and Francisco J. Enguita. "Structural Insights into Carboxylic Polyester-Degrading Enzymes and Their Functional Depolymerizing Neighbors." International Journal of Molecular Sciences 22, no. 5 (2021): 2332. http://dx.doi.org/10.3390/ijms22052332.

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Esters are organic compounds widely represented in cellular structures and metabolism, originated by the condensation of organic acids and alcohols. Esterification reactions are also used by chemical industries for the production of synthetic plastic polymers. Polyester plastics are an increasing source of environmental pollution due to their intrinsic stability and limited recycling efforts. Bioremediation of polyesters based on the use of specific microbial enzymes is an interesting alternative to the current methods for the valorization of used plastics. Microbial esterases are promising ca

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9

Short, Gabriel N., Ha T. H. Nguyen, Patricia I. Scheurle, and Stephen A. Miller. "Aromatic polyesters from biosuccinic acid." Polymer Chemistry 9, no. 30 (2018): 4113–19. http://dx.doi.org/10.1039/c8py00862k.

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10

Han, H. "Wholly aromatic liquid-crystalline polyesters." Progress in Polymer Science 22, no. 7 (1997): 1431–502. http://dx.doi.org/10.1016/s0079-6700(96)00028-7.

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11

Zhang, Li, and Wei-Yuan Huang. "Synthesis of polyfluorinated aromatic polyesters." Journal of Fluorine Chemistry 102, no. 1-2 (2000): 55–59. http://dx.doi.org/10.1016/s0022-1139(99)00245-6.

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12

Economy, J. "Aromatic Polyesters ofp-Hydroxybenzoic Acid." Molecular Crystals and Liquid Crystals Incorporating Nonlinear Optics 169, no. 1 (1989): 1–22. http://dx.doi.org/10.1080/00268948908062731.

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13

Kricheldorf, Hans R., Lars Wahlen, and Thomas Stukenbrook. "Biodegradable liquid-crystalline aromatic polyesters." Macromolecular Symposia 130, no. 1 (1998): 261–70. http://dx.doi.org/10.1002/masy.19981300123.

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14

Kultys, Anna. "Polyesters containing sulfur. VII. New aliphatic-aromatic polyesters for synthesis of polyester-sulfur compositions and polyurethanes." Journal of Polymer Science Part A: Polymer Chemistry 37, no. 6 (1999): 835–48. http://dx.doi.org/10.1002/(sici)1099-0518(19990315)37:6<835::aid-pola19>3.0.co;2-y.

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15

Wagner-Egea, Paula, Virginia Tosi, Ping Wang, Carl Grey, Baozhong Zhang, and Javier A. Linares-Pastén. "Assessment of IsPETase-Assisted Depolymerization of Terephthalate Aromatic Polyesters and the Effect of the Thioredoxin Fusion Domain." Applied Sciences 11, no. 18 (2021): 8315. http://dx.doi.org/10.3390/app11188315.

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Terephthalate polyesters such as poly(ethylene terephthalate) (PET) have been massively produced over the last few decades due to their attractive properties in multiple applications. However, due to their limited biodegradability, they have accumulated in landfills and oceans, posing an environmental threat. Enzymatic recycling technologies are predicted to generate long-term socioeconomic benefits. In the present work, we compared the IsPETase (from Ideonella sakaiensis 201-F6) activity on a series of polyesters, including poly(butylene) terephthalate (PBT), poly(hexamethylene) terephthalate

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16

SASANUMA, Yuji, and Nobuaki SUZUKI. "Structure—Property Relationships of Aromatic Polyesters." KOBUNSHI RONBUNSHU 67, no. 1 (2010): 1–9. http://dx.doi.org/10.1295/koron.67.1.

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17

Müller, Rolf-Joachim, Ilona Kleeberg, and Wolf-Dieter Deckwer. "Biodegradation of polyesters containing aromatic constituents." Journal of Biotechnology 86, no. 2 (2001): 87–95. http://dx.doi.org/10.1016/s0168-1656(00)00407-7.

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18

Kricheldorf, H. R. "Star shaped and hyperbranched aromatic polyesters." Pure and Applied Chemistry 70, no. 6 (1998): 1235–38. http://dx.doi.org/10.1351/pac199870061235.

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19

Wu, X. Y., Y.-Y. Linko, J. Sepp�l�, M. Leisola, and P. Linko. "Lipase-catalyzed synthesis of aromatic polyesters." Journal of Industrial Microbiology and Biotechnology 20, no. 6 (1998): 328–32. http://dx.doi.org/10.1038/sj.jim.2900533.

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20

Sinta, R., R. A. Minns, R. A. Gaudiana, and H. G. Rogers. "Soluble, amorphous, para-linked aromatic polyesters." Journal of Polymer Science Part C: Polymer Letters 25, no. 1 (1987): 11–17. http://dx.doi.org/10.1002/pol.1987.140250103.

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21

Wang, Ping, and Baozhong Zhang. "Sustainable aromatic polyesters with 1,5-disubstituted indole units." RSC Advances 11, no. 27 (2021): 16480–89. http://dx.doi.org/10.1039/d1ra02197d.

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22

Kausar, Ayesha. "Review of fundamentals and applications of polyester nanocomposites filled with carbonaceous nanofillers." Journal of Plastic Film & Sheeting 35, no. 1 (2018): 22–44. http://dx.doi.org/10.1177/8756087918783827.

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Polyester is a versatile commercially significant polymer (thermoplastic/thermoset) well-known for its biodegradability and excellent thermal, mechanical, and chemical properties. Synthetic aromatic polyester resins usually have better moisture resistance, nonflammability, liquid crystal, strength, thermal, and environmental features compared with natural/aliphatic polyesters. Nanofillers can reinforce these important polymers to further enhance the final nanocomposite structural and physical characteristics. This review presents research devoted to polyester nanocomposites with essential nano

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23

Wagner-Egea, Paula, Lucía Aristizábal-Lanza, Cecilia Tullberg, et al. "Marine PET Hydrolase (PET2): Assessment of Terephthalate- and Indole-Based Polyester Depolymerization." Catalysts 13, no. 9 (2023): 1234. http://dx.doi.org/10.3390/catal13091234.

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Enzymatic polyethylene terephthalate (PET) recycling processes are gaining interest for their low environmental impact, use of mild conditions, and specificity. Furthermore, PET hydrolase enzymes are continuously being discovered and engineered. In this work, we studied a PET hydrolase (PET2), initially characterized as an alkaline thermostable lipase. PET2 was produced in a fusion form with a 6-histidine tag in the N-terminal. The PET2 activity on aromatic terephthalate and new indole-based polyesters was evaluated using polymers in powder form. Compared with IsPETase, an enzyme derived from

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24

D’Auria, Ilaria, Sara D’Aniello, Gianluca Viscusi, et al. "One-Pot Terpolymerization of Macrolactones with Limonene Oxide and Phtalic Anhydride to Produce di-Block Semi-Aromatic Polyesters." Polymers 14, no. 22 (2022): 4911. http://dx.doi.org/10.3390/polym14224911.

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The synthesis of novel block copolymers, namely poly(limonene-phthalate)-block-poly(pentadecalactone) and poly(limonene-phthalate)-block-poly(pentadecalactone) is here described. To achieve this synthesis, a bimetallic aluminum based complex (1) was used as catalyst in the combination of two distinct processes: the ring-opening polymerization (ROP) of macrolactones such as ω-pentadecalactone (PDL) and ω-6-hexadecenlactone (HDL) and the ring-opening copolymerization (ROCOP) of limonene oxide (LO) and phthalic anhydride (PA). The synthesis of di-block polyesters was performed in a one-pot proced

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25

SUEOKA, Kenji, Yoshimi NAGAI, Masatoshi NAGATA, and Sadao SEGAWA. "Compositional analysis of liquid crystalline aromatic polyesters." Analytical Sciences 6, no. 3 (1990): 371–74. http://dx.doi.org/10.2116/analsci.6.371.

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26

Hall, Henry, Samiul Ahad, Robert Bates, et al. "Structural Analysis of Aromatic Liquid Crystalline Polyesters." Polymers 3, no. 1 (2011): 367–87. http://dx.doi.org/10.3390/polym3010367.

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27

Kim, Hee Joong, Yernaidu Reddi, Christopher J. Cramer, Marc A. Hillmyer, and Christopher J. Ellison. "Readily Degradable Aromatic Polyesters from Salicylic Acid." ACS Macro Letters 9, no. 1 (2020): 96–102. http://dx.doi.org/10.1021/acsmacrolett.9b00890.

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28

Chung, Sung-Jae, Kong-Kyum Kim, and Jung-Il Jin. "Fluorescing wholly aromatic polyesters containing diphenylanthracene fluorophores." Polymer 40, no. 8 (1999): 1943–53. http://dx.doi.org/10.1016/s0032-3861(98)00420-0.

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29

Yoon, H. N. "Strength of fibers from wholly aromatic polyesters." Colloid & Polymer Science 268, no. 3 (1990): 230–39. http://dx.doi.org/10.1007/bf01490247.

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30

Lautenschlaeger, P., J. Brickmann, Jippe Van Ruiten, and Robert J. Meier. "Conformations and rotational barriers of aromatic polyesters." Macromolecules 24, no. 6 (1991): 1284–92. http://dx.doi.org/10.1021/ma00006a012.

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31

Zhang, Xinli. "Hyperbranched aromatic polyesters: From synthesis to applications." Progress in Organic Coatings 69, no. 4 (2010): 295–309. http://dx.doi.org/10.1016/j.porgcoat.2010.08.007.

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32

Cai, Rubing, and Edward T. Samulski. "Liquid-crystalline aromatic polyesters containing isophthalic acid." Macromolecules 27, no. 1 (1994): 135–40. http://dx.doi.org/10.1021/ma00079a020.

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33

Lodha, A., R. S. Ghadage, and S. Ponrathnam. "Polycondensation reaction kinetics of wholly aromatic polyesters." Polymer 38, no. 25 (1997): 6167–74. http://dx.doi.org/10.1016/s0032-3861(97)00183-3.

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34

Shin, Sei-Moon, Dong-Keun Shin, and Dong-Choo Lee. "Toughening of epoxy resins with aromatic polyesters." Journal of Applied Polymer Science 78, no. 14 (2000): 2464–73. http://dx.doi.org/10.1002/1097-4628(20001227)78:14<2464::aid-app50>3.0.co;2-5.

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35

Choi, Woon-Seop, Anne Buyle Padias, and H. K. Hall. "LCP aromatic polyesters by esterolysis melt polymerization." Journal of Polymer Science Part A: Polymer Chemistry 38, no. 19 (2000): 3586–95. http://dx.doi.org/10.1002/1099-0518(20001001)38:19<3586::aid-pola140>3.0.co;2-j.

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36

Coussensa, Betty, K. Pierloot, and Robert J. Meier. "Conformations and rotational barriers of aromatic polyesters." Journal of Molecular Structure: THEOCHEM 259 (July 1992): 331–44. http://dx.doi.org/10.1016/0166-1280(92)87023-s.

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37

Fodor, Csaba, Milad Golkaram, Albert J. J. Woortman, Jur van Dijken, and Katja Loos. "Enzymatic approach for the synthesis of biobased aromatic–aliphatic oligo-/polyesters." Polymer Chemistry 8, no. 44 (2017): 6795–805. http://dx.doi.org/10.1039/c7py01559c.

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38

Ma, Meng Meng, Lian Yuan Wang, and Hai Yan Zhu. "Enzymatic Degradation of Polyester-Nanoparticles by Lipases and Adsorption of Lipases on the Polyester-Nanoparticles." Advanced Materials Research 418-420 (December 2011): 2302–7. http://dx.doi.org/10.4028/www.scientific.net/amr.418-420.2302.

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Enzymatic degradation tests of polymer in form of nanoparticle (NP) were used to study the biodegradation of two different types of polymers polytetramethylene adipitate (SP4/6) and polybutylene isophthalate (PBI) by two commercially available lipases. The two lipases, which are from the yeast Candida cylindracea (CcL) and Pseudomonas species (PsL) respectively, exhibited sufficient degradation activities both for the aliphatic model polyester SP4/6 and the aromatic model polyester PBI and the use of polyester NPs has dramatically shortened the duration of enzymatic degradation tests. It has a

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39

Guan, Xing-Hua, He-Ran Nie, Hong-Hua Wang, et al. "High-solubility aromatic polyesters with fluorene and phthalein groups: Synthesis and property." High Performance Polymers 32, no. 8 (2020): 933–44. http://dx.doi.org/10.1177/0954008320912314.

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A series of aromatic polyesters bearing fluorene and phthalein groups were synthesized from commercially available 9,9-bis(4-hydroxyphenyl)fluorene (BPF), phenolphthalein, and terephthaloyl chloride through an interfacial polymerization method. The microstructure, molecular weight, morphology, thermal properties, and thermal decomposition mechanism of these aromatic polyesters were investigated. Their mechanical properties were also evaluated. The results suggested that the copolymer compositions were approximately equal to the feed compositions. Moreover, the increase in the BPF unit content

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40

Vayshbeyn, Leonid Ilyich, Elena Evgenyevna Mastalygina, Anatoly Aleksandrovich Olkhov, and Maria Victorovna Podzorova. "Poly(lactic acid)-Based Blends: A Comprehensive Review." Applied Sciences 13, no. 8 (2023): 5148. http://dx.doi.org/10.3390/app13085148.

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Aliphatic and aromatic polyesters of hydroxycarboxylic acids are characterized not only by biodegradability, but also by biocompatibility and inertness, which makes them suitable for use in different applications. Polyesters with high enzymatic hydrolysis capacity include poly(lactic acid), poly(ε-caprolactone), poly(butylene succinate) and poly(butylene adipate-co-terephthalate), poly(butylene succinate-co-adipate). At the same time, poly(lactic acid) is the most durable, widespread, and cheap polyester from this series. However, it has a number of drawbacks, such as high brittleness, narrow

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41

Nagasawa, Masayuki, Tatsuya Ishii, Daisuke Abe, and Yuji Sasanuma. "Structure–property relationships of aromatic polyamides and polythioamides: comparative consideration with those of analogous polyesters, polythioesters and polydithioesters." RSC Advances 5, no. 117 (2015): 96611–22. http://dx.doi.org/10.1039/c5ra17883e.

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42

Didenko, A. L., A. G. Ivanov, V. E. Smirnova, et al. "Comparative characteristics of products of processing of fusible copoly (urethane-imides) from the solutions and melts formed by them." Plasticheskie massy, no. 9-10 (November 29, 2022): 20–24. http://dx.doi.org/10.35164/0554-2901-2022-9-10-20-24.

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Self-supporting films and thick-walled moldings (blades) were obtained from solutions and melts of multiblock (segmental) copoly(urethane-imides). The initial copoly(urethane-imides) were obtained on the basis of aliphatic polyesters: poly(propyleneglycol), poly(diethyleneglycoladipinate) and polycaprolactone, dianhydride of 1,3-bis(3’,4-dicarboxyphenoxy) benzene and aromatic diamines: 4,4’-bis-(4”-aminophenoxy)biphenyl and 1,4-bis(4’-aminophenoxy)diphenylsulfone. Samples of films and moldings were studied by IR spectroscopy, TGA, DSC and mechanical analysis under static and dynamic (DMA) expe

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43

Koelewijn, S. F., C. Cooreman, T. Renders, et al. "Promising bulk production of a potentially benign bisphenol A replacement from a hardwood lignin platform." Green Chemistry 20, no. 5 (2018): 1050–58. http://dx.doi.org/10.1039/c7gc02989f.

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44

Llevot, Audrey, Etienne Grau, Stéphane Carlotti, Stéphane Grelier, and Henri Cramail. "Renewable (semi)aromatic polyesters from symmetrical vanillin-based dimers." Polymer Chemistry 6, no. 33 (2015): 6058–66. http://dx.doi.org/10.1039/c5py00824g.

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Two symmetrical biphenyl monomers derived from vanillin, a methylated divanillyl diol and a methylated dimethylvanillate dimer, were synthesized and employed as (co)monomers for the design of renewable (semi)aromatic polyesters.

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45

Sokołowska, Martyna, Jagoda Nowak-Grzebyta, Ewa Stachowska, et al. "Enzymatically catalyzed furan-based copolyesters containing dilinoleic diol as a building block." RSC Advances 13, no. 32 (2023): 22234–49. http://dx.doi.org/10.1039/d3ra03885h.

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Enzymatically-catalyzed polycondensation as more environmentally friendly method for creating sustainable alternatives to traditional aromatic–aliphatic polyesters is a valuable step towards resource-efficiency optimization.

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46

Fu, Teng, De-Ming Guo, Jia-Ning Wu, et al. "Inherent flame retardation of semi-aromatic polyesters via binding small-molecule free radicals and charring." Polymer Chemistry 7, no. 8 (2016): 1584–92. http://dx.doi.org/10.1039/c5py01938a.

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47

Хараев, Арсен Мухамедович, and Рима Чамаловна Бажева. "STUDY OF RELAXATION TRANSITIONS IN SOME AROMATIC POLYESTERS." Physical and Chemical Aspects of the Study of Clusters, Nanostructures and Nanomaterials, no. 13 (December 23, 2021): 928–36. http://dx.doi.org/10.26456/pcascnn/2021.13.928.

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Методом спинового зонда проведено систематическое изучение основных релаксационных переходов жесткоцепных стеклообразных полимеров в широком интервале температур с применением спиновых зондов разного размера на примере полисульфона. В главной области релаксации ароматических полиэфиров с помощью метода спинового зонда обнаружены два перегиба. Два перегиба, обнаруженные на температурной зависимости времени корреляции вращения, являются следствием размораживания сегментальной подвижности в областях с различной упаковкой сегментов. Показано, что высокотемпературный перегиб соответствует разморажи

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48

Nakayama, Atsushi, Ryosuke Takahashi, Tsubasa Hamano, Taiyo Yoshioka, and Masaki Tsuji. "Morphological Study on Electrospun Nanofibers of Aromatic Polyesters." FIBER 64, no. 1 (2008): 32–35. http://dx.doi.org/10.2115/fiber.64.32.

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49

Mikitaev, A. K., A. Yu Bedanokov, and M. A. Mikitaev. "New approaches to the synthesis of aromatic polyesters." Russian Journal of General Chemistry 79, no. 9 (2009): 1998–2005. http://dx.doi.org/10.1134/s107036320909031x.

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50

Xueqiu, Wang, Wu Hojung, and Li Shijin. "Synthesis and mesomorphic behaviour of some aromatic polyesters." Liquid Crystals 3, no. 9 (1988): 1267–74. http://dx.doi.org/10.1080/02678298808086583.

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