Characteristics and Kinetics Study of Glycerolabietate from Glycerol and Abietic Acid from Rosin

https://doi.org/10.22146/jrekpros.69206

Danang Tri Hartanto(1*), Rochmadi Rochmadi(2), Meiga Putri Wahyu(3), Diastari Kusumawati(4)

(1) Faculty of Engineering Universitas Gadjah Mada, Yogyakarta
(2) Faculty of Engineering Universitas Gadjah Mada, Yogyakarta
(3) Faculty of Engineering Universitas Gadjah Mada, Yogyakarta
(4) Faculty of Engineering Universitas Gadjah Mada, Yogyakarta
(*) Corresponding Author

Abstract


Rosin is a natural resin from the coniferous tree sap, which separated from its oil content (terpenes). Rosin is brittle. Therefore modifications are needed to improve its mechanical properties. The main content of rosin is abietic acid which has a carboxylic group, so it can form an ester group when reacted with polyhydric alcohol (polyalcohol) such as glycerol. The research aimed to study the kinetics of the esterification reaction between the hydroxyl group in glycerol and the carboxylic group in abietic acid from rosin at various reaction temperatures and reactant compositions. This reaction is carried out in a three-neck flask at atmospheric pressure without a catalyst. The reaction temperatures used were 180˚C, 200˚C, and 220˚C, and the ratio of rosin and glycerol was 1:1, 1:3, and 1:5. The reaction kinetics calculations were analyzed with acid number data over the reaction time using three different models. The calculations showed that this reaction involves positioning a hydroxyl group on glycerol, which the primary and secondary hydroxyl groups contribute to forming a rosin ester (glycerolabietate). The rate of reaction constants of primary hydroxyl of glycerol and abietic acid were in the range 6.25x10-4 - 3.90x10-3 g/(mgeq.min), while reaction rate constants of secondary hydroxyl and abietic acid were in the range 1.06x10-5 - 1.15x10-4 g/(mgeq.min). FTIR analysis showed a change in the hydroxyl, carboxylate, and ester groups which were assigned by a shift of wavenumber and a difference of intensity at 3200-3570 cm-1, 1697.36 cm-1, and 1273.02 cm-1.


Keywords


acid number; glycerol; glycerolabietate; hydroxyl group; rosin-ester;

Full Text:

PDF


References

Bayu, A., Nandiyanto, D., Oktiani, R. and Ragadhita, R., 2019, Indonesian Journal of Science & Technology How to Read and Interpret FTIR Spectroscope of Organic Material, Indones. J. Sci. Technol., 4 (1), 97–118. Domene-López, D., Guillén, M.M., Martin-Gullon, I., García-Quesada, J.C. and Montalbán, M.G., 2018, Study of the behavior of biodegradable starch/polyvinyl alcohol/rosin blends, Carbohydr. Polym., Elsevier, 202 (September), 299–305. Gandini, A. and Lacerda, T.M., 2015, From monomers to polymers from renewable resources: Recent advances, Prog. Polym. Sci., Elsevier Ltd, 48, 1–39. García, D.F., Bustamante, F., Villa, A.L. and Alarcón, E.A., 2021, Esterification of rosin with methyl alcohol for fuel applications, Redin (100), 10–20. Hartanto, D. T., Rochmadi, Budhijanto, 2020, Mechanism and kinetic model for glycerolysis of shellac, IOP Conf. Ser. Mater. Sci. Eng., 778, 012053. Hsieh, C.C. and Chen, Y.C., 2020, Synthesis of bio-based polyurethane foam modified with rosin using an environmentally-friendly process, J. Clean. Prod., Elsevier Ltd, 276, 124203. Kugler, S., Ossowicz, P., Malarczyk-Matusiak, K. and Wierzbicka, E., 2019, Advances in rosin-based chemicals: The latest recipes, applications and future trends, Molecules, 24 (9), available at:https://doi.org/10.3390/molecules24091651. Kumooka, Y., 2008, analysis of rosin and modified rosin esters in adhesives by matrix-assisted laser desorption/ionization time-of-flight mass spectrometry (MALDI-TOF-MS), Forensic Sci. Int., 176 (2–3), 111–120. Ladero, M., de Gracia, M., Tamayo, J.J., Ahumada, I.L. de, Trujillo, F. and Garcia-Ochoa, F., 2011, Kinetic modelling of the esterification of rosin and glycerol: Application to industrial operation, Chem. Eng. J., Elsevier B.V., 169 (1–3), 319–328. Ladero, M., de Gracia, M., Trujillo, F. and Garcia-Ochoa, F., 2012, Phenomenological kinetic modelling of the esterification of rosin and polyols, Chem. Eng. J., Elsevier B.V., 197, 387–397. Lin, R., Li, H., Long, H., Su, J. and Huang, W., 2014, Synthesis of Rosin Acid Starch Catalyzed by Lipase, 2014. Mumtaz, I., Majeed, Z., Ajab, Z., Ahmad, B., Khurshid, K. and Mubashir, M., 2019, Optimized tuning of rosin adduct with maleic anhydride for smart applications in controlled and targeted delivery of urea for higher plant's uptake and growth efficiency, Ind. Crops Prod., Elsevier, 133 (March), 395–408. Satriana, S. and Supardan, M.D., 2008, Kinetic Study of Esterification of Free Fatty Acid in Low Grade Crude Palm Oil using Sulfuric Acid, ASEAN J. Chem. Eng., 8 (1 & 2), 1. Su, N., Fang, C., Zhou, H., Tang, T., Zhang, S. and Fei, B., 2021, Hydrophobic treatment of bamboo with rosin, Constr. Build. Mater., 271, available at:https://doi.org/10.1016/j.conbuildmat.2020.121507. Sun, S., Cheng, X., Ma, M., Liu, Y., Wang, G., Yu, H., Liu, S., et al., 2021, High-efficient esterification of rosin and glycerol catalyzed by novel rare earth Lewis acidic ionic liquid: Reaction development and mechanistic study, J. Taiwan Inst. Chem. Eng., Elsevier B.V., 000, available at:https://doi.org/10.1016/j.jtice.2021.07.026. Xu, Z., Lou, W., Zhao, G., Zhang, M., Hao, J. and Wang, X., 2019, Pentaerythritol rosin ester as an environmentally friendly multifunctional additive in vegetable oil-based lubricant, Tribol. Int., Elsevier Ltd, 135 (February), 213–218. Zhou, D., Chen, X., Liang, B., Fan, X., Wei, X., Liang, J. and Wang, L., 2019, Embedding MIL-100(Fe) with magnetically recyclable Fe3O4 nanoparticles for highly efficient esterification of diterpene resin acids and the associated kinetics, Microporous Mesoporous Mater., 289 (July), available at:https://doi.org/10.1016/j.micromeso.2019.109615.



DOI: https://doi.org/10.22146/jrekpros.69206

Article Metrics

Abstract views : 2026 | views : 1321

Refbacks

  • There are currently no refbacks.




Copyright (c) 2021 The authors

Creative Commons License
This work is licensed under a Creative Commons Attribution-ShareAlike 4.0 International License.