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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Main Authors: Ana Jurkeviciute, Larisa Grigorieva, Kaia Tõnsuaadu, Tamara Yashicheva, Dmitrij Bondarev
Format: Article
Language:English
Published: IOP Publishing 2023-01-01
Series:Materials Research Express
Subjects:
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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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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AT kaiatonsuaadu nonaldehyderesinsbasedonresorcinolandnaturalalkylresorcinolsmodifiedwithstyrene
AT tamarayashicheva nonaldehyderesinsbasedonresorcinolandnaturalalkylresorcinolsmodifiedwithstyrene
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