Non-aldehyde resins based on resorcinol and natural alkylresorcinols modified with styrene
The use of natural alkylresorcinols produced in Estonia (5-methylresorcinol, HONEYOL80 fraction) instead of the expensive resorcinol reduces the cost of the synthesized resins while maintaining their high technological characteristics. Resins based on resorcinol (R), 5-methylresorcinol (5-MR), HONEY...
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IOP Publishing
2023-01-01
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Series: | Materials Research Express |
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Online Access: | https://doi.org/10.1088/2053-1591/acfd12 |
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author | Ana Jurkeviciute Larisa Grigorieva Kaia Tõnsuaadu Tamara Yashicheva Dmitrij Bondarev |
author_facet | Ana Jurkeviciute Larisa Grigorieva Kaia Tõnsuaadu Tamara Yashicheva Dmitrij Bondarev |
author_sort | Ana Jurkeviciute |
collection | DOAJ |
description | The use of natural alkylresorcinols produced in Estonia (5-methylresorcinol, HONEYOL80 fraction) instead of the expensive resorcinol reduces the cost of the synthesized resins while maintaining their high technological characteristics. Resins based on resorcinol (R), 5-methylresorcinol (5-MR), HONEYOL80, dicyclopentadiene (DCPD), and styrene (S) were synthesized in the presence of an acid catalyst. Their physical and chemical characteristics have also been studied. It was shown that depending on the mole ratio of the components of the formulation, resins with different softening temperatures (66 to 97 °C), ash content of 0.04 to 0.39 wt%, and a low content of volatile components at 105 °C, including moisture, were obtained. The best conditions for the synthesis of resins with a softening point of 94 °C–97 °C are molar ratio of R (5-MR): DCPD: S = 1: 0.5: 0.3 at temperature 135 °C–170 °C, synthesis time 5 h 30 min. The synthesized resins did not require additional processing under a vacuum. The presence of unreacted resorcinol and 5-methylresorcinol (quantitatively and qualitatively) in the final product, the homogeneity, and molecular weight characteristics of the resin composition (qualitatively) were determined by TLC and GPC. |
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issn | 2053-1591 |
language | English |
last_indexed | 2024-03-11T19:42:19Z |
publishDate | 2023-01-01 |
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series | Materials Research Express |
spelling | doaj.art-429dcccc8a91480ba7e21d84884ebb1c2023-10-06T07:35:05ZengIOP PublishingMaterials Research Express2053-15912023-01-01101010530110.1088/2053-1591/acfd12Non-aldehyde resins based on resorcinol and natural alkylresorcinols modified with styreneAna Jurkeviciute0https://orcid.org/0000-0002-9175-1963Larisa Grigorieva1https://orcid.org/0000-0002-2409-1061Kaia Tõnsuaadu2Tamara Yashicheva3Dmitrij Bondarev4Department of Materials and Environmental Technology, Tallinn University of Technology , Ehitajate tee 5, 19086 Tallinn, EstoniaLaboratory of Fuels Technology, Virumaa College of Tallinn University of Technology , Järveküla tee 75, 30322, Kohtla-Järve, EstoniaDepartment of Materials and Environmental Technology, Tallinn University of Technology , Ehitajate tee 5, 19086 Tallinn, EstoniaVirumaa College of Tallinn University of Technology , Järveküla tee 75, 30322, Kohtla-Järve, EstoniaPolymer Institute SAS, Dúbravská cesta 9, 84541 Bratislava, SlovakiaThe use of natural alkylresorcinols produced in Estonia (5-methylresorcinol, HONEYOL80 fraction) instead of the expensive resorcinol reduces the cost of the synthesized resins while maintaining their high technological characteristics. Resins based on resorcinol (R), 5-methylresorcinol (5-MR), HONEYOL80, dicyclopentadiene (DCPD), and styrene (S) were synthesized in the presence of an acid catalyst. Their physical and chemical characteristics have also been studied. It was shown that depending on the mole ratio of the components of the formulation, resins with different softening temperatures (66 to 97 °C), ash content of 0.04 to 0.39 wt%, and a low content of volatile components at 105 °C, including moisture, were obtained. The best conditions for the synthesis of resins with a softening point of 94 °C–97 °C are molar ratio of R (5-MR): DCPD: S = 1: 0.5: 0.3 at temperature 135 °C–170 °C, synthesis time 5 h 30 min. The synthesized resins did not require additional processing under a vacuum. The presence of unreacted resorcinol and 5-methylresorcinol (quantitatively and qualitatively) in the final product, the homogeneity, and molecular weight characteristics of the resin composition (qualitatively) were determined by TLC and GPC.https://doi.org/10.1088/2053-1591/acfd12resorcinol5-methylresorcinolnatural alkylresorcinolsfraction HONEYOL80dicyclopentadienestyrene |
spellingShingle | Ana Jurkeviciute Larisa Grigorieva Kaia Tõnsuaadu Tamara Yashicheva Dmitrij Bondarev Non-aldehyde resins based on resorcinol and natural alkylresorcinols modified with styrene Materials Research Express resorcinol 5-methylresorcinol natural alkylresorcinols fraction HONEYOL80 dicyclopentadiene styrene |
title | Non-aldehyde resins based on resorcinol and natural alkylresorcinols modified with styrene |
title_full | Non-aldehyde resins based on resorcinol and natural alkylresorcinols modified with styrene |
title_fullStr | Non-aldehyde resins based on resorcinol and natural alkylresorcinols modified with styrene |
title_full_unstemmed | Non-aldehyde resins based on resorcinol and natural alkylresorcinols modified with styrene |
title_short | Non-aldehyde resins based on resorcinol and natural alkylresorcinols modified with styrene |
title_sort | non aldehyde resins based on resorcinol and natural alkylresorcinols modified with styrene |
topic | resorcinol 5-methylresorcinol natural alkylresorcinols fraction HONEYOL80 dicyclopentadiene styrene |
url | https://doi.org/10.1088/2053-1591/acfd12 |
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