Catalytic Disproportionation of Indonesian Gum Rosin over Pd/C Catalyst: GC–MS Analysis and Reaction Mechanism
DOI:
https://doi.org/10.31315/eksergi.v23i1.15831Keywords:
gum rosin, disproportionation, resin acids, mercusic acid, Pd/C catalystAbstract
Indonesian gum rosin is a renewable natural resource with a unique composition characterized by the presence of mercusic acid. This study investigates its catalytic disproportionation over a Pd/C catalyst in a sealed batch reactor at 200 °C and 240 °C to improve chemical stability and explore its reactivity. The reaction products were analyzed using FTIR and GC–MS after methylation. Abietic acid was identified as the most reactive resin acid, undergoing typical disproportionation into hydrogenated (e.g., dihydroabietic) and dehydrogenated (dehydroabietic) derivatives. The formation of dehydroabietic acid was favored at 200 °C, while higher temperature (240 °C) promoted hydrogenation and isomerization side reactions. In contrast, mercusic acid followed a distinct pathway, undergoing selective double-bond isomerization to form structural isomers without changes in molecular weight, as confirmed by identical molecular ions (m/z 364) in the mass spectra. These findings clarify the temperature-dependent reaction behavior of major resin acids and reveal the unique mechanistic role of mercusic acid in Indonesian gum rosin.
References
Comyn, J. (1994). Surface characterization of pentaerythritol rosin ester. Int. J. Adhes. Adhes, 15, 9–14. https://doi.org/https://doi.org/10.1016/0143-7496(95)93637-Z
Gu, Y., Li, Y., Zhang, J., Zhang, H., Wu, C., Lin, J., Zhou, J., Fan, Y., Murugadoss, V., & Guo, Z. (2020). Effects of pretreated carbon supports in Pd/C catalysts on rosin disproportionation catalytic performance. Chemical Engineering Science, 216. https://doi.org/10.1016/j.ces.2020.115588
Hardhianti, M. P. W., Rochmadi, & Azis, M. M. (2022). Kinetic studies of esterification of rosin and pentaerythritol. Processes, 10(1). https://doi.org/10.3390/pr10010039
Hartanto, D. T., Rochmadi, Hardhianti, M. P. W., & Kusumawati, D. (2021). Characteristics and Kinetics Study of Glycerolabietate from Glycerol and Abietic Acid from Rosin. Jurnal Rekayasa Proses, 15(2), 170. https://doi.org/10.22146/jrekpros.69206
Kugler, S., Ossowicz, P., Malarczyk-Matusiak, K., & Wierzbicka, E. (2019). Advances in rosin-based chemicals: The latest recipes, applications and future trends. Molecules, 24(9). https://doi.org/10.3390/molecules24091651
Kumar, R., Chattopadhyay, K., Bhasker, B., Mondal, S., Christopher, J., & Kapur, G. S. (2018). Rapid method for determination of dehydro abietic acid in gum rosin and disproportionate rosin by proton nuclear magnetic resonance spectroscopy. European Journal of Sciences (EJS), 35–42. https://doi.org/10.29198/ejs1804
Ladero, M., de Gracia, M., Trujillo, F., & Garcia-Ochoa, F. (2012). Phenomenological kinetic modelling of the esterification of rosin and polyols. Chemical Engineering Journal, 197, 387–397. https://doi.org/10.1016/j.cej.2012.05.053
Maiti, S., Ray, N., & Kundu, A. K. (1989). Rosin: A Renewable Resource for Polymers and Polymer Chemicals. Prog. Polym. Sci, 14, 297–338. https://doi.org/https://doi.org/10.1016/0079-6700(89)90005-1
Mostafalu, R., Heydari, A., Banaei, A., Ghorbani, F., & Arefi, M. (2017). The use of palladium nanoparticles supported on active carbon for synthesis of disproportionate rosin (DPR). Journal of Nanostructure in Chemistry, 7(1), 61–66. https://doi.org/10.1007/s40097-017-0220-y
Pathak, Y. V., & Dorle, A. K. (1987). Study of Rosin and Rosin Derivatives as Coating Materials for Controlled Release of Drug. Journal of Controlled Release, 5, 63–68. https://doi.org/https://doi.org/10.1016/0168-3659(87)90038-1
Silvestre, A. J. D., & Gandini, A. (2008). Rosin: Major Sources, Properties and Applications. In Monomers, Polymers and Composites from Renewable Resources (pp. 67–88). Elsevier. https://doi.org/https://doi.org/10.1016/B978-0-08-045316-3.00004-1
Souto, J. C., Yustos, P., Garcia-Ochoa, F., & Ladero, M. (2024). Disproportionation of Rosin Driven by 4,4′-Thio-bis(3-Methyl-6-Tert-Butylphenol): Kinetic Model Discrimination. Catalysts, 14(4). https://doi.org/10.3390/catal14040235
Souto, J. C., Yustos, P., Ladero, M., & Garcia-Ochoa, F. (2011). Disproportionation of rosin on an industrial Pd/C catalyst: Reaction pathway and kinetic model discrimination. Bioresource Technology, 102(3), 3504–3511. https://doi.org/10.1016/j.biortech.2010.11.022
Tanaka, R., Tokuda, H., & Ezaki, Y. (2008). Cancer chemopreventive activity of “rosin” constituents of Pinus spez. and their derivatives in two-stage mouse skin carcinogenesis test. Phytomedicine, 15(11), 985–992. https://doi.org/10.1016/j.phymed.2008.02.020
Wang, L., Chen, X., Liang, J., Chen, Y., Pu, X., & Tong, Z. (2009). Kinetics of the catalytic isomerization and disproportionation of rosin over carbon-supported palladium. Chemical Engineering Journal, 152(1), 242–250. https://doi.org/10.1016/j.cej.2009.04.052
Wang, L., Chen, X., Sun, W., Liang, J., Xu, X., & Tong, Z. (2013). Kinetic model for the catalytic disproportionation of pine oleoresin over Pd/C catalyst. Industrial Crops and Products, 49, 1–9. https://doi.org/10.1016/j.indcrop.2013.04.015
Wiyono, B., Tachibana, S., & Tinambunan, D. (2006). Chemical Composition of Indonesian Pinus merkusii Turpentine Oils, Gum Oleoresins and Rosins from Sumatra and Java. Pakistan Journal of Biological Sciences, 9, 7–14. https://doi.org/https://doi.org/10.3923/pjbs.2006.7.14
Xu, Z., Lou, W., Zhao, G., Zhang, M., Hao, J., & Wang, X. (2019). Pentaerythritol rosin ester as an environmentally friendly multifunctional additive in vegetable oil-based lubricant. Tribology International, 135, 213–218. https://doi.org/10.1016/j.triboint.2019.02.038
Zhang, D., Zhou, D., Wei, X., Liang, J., Chen, X., & Wang, L. (2017). Green catalytic conversion of hydrogenated rosin to glycerol esters using subcritical CO2 in water and the associated kinetics. Journal of Supercritical Fluids, 125, 12–21. https://doi.org/10.1016/j.supflu.2017.01.009
Downloads
Published
How to Cite
Issue
Section
License
Copyright (c) 2026 Meiga Putri Wahyu Hardhianti

This work is licensed under a Creative Commons Attribution-ShareAlike 4.0 International License.
Authors who publish with this journal agree to the following terms:
Authors retain copyright and grant the journal right of first publication with the work simultaneously licensed under a Creative Commons Attribution-ShareAlike 4.0 International License(CC BY SA 4.0) that allows others to share the work with an acknowledgement of the work's authorship and initial publication in this journal.
Authors are able to enter into separate, additional contractual arrangements for the non-exclusive distribution of the journal's published version of the work (e.g., post it to an institutional repository or publish it in a book), with an acknowledgement of its initial publication in this journal.
Authors are permitted and encouraged to post their work online (e.g., in institutional repositories or on their website) prior to and during the submission process, as it can lead to productive exchanges, as well as earlier and greater citation of published work (See The Effect of Open Access).
Eksergi allows authors retain the copyright and full publishing rights without restrictions.



