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Effect of alkali content and synthesis duration on the properties of lignin-phenol-formaldehyde resins prepared with technical lignosulfonates

https://doi.org/10.21266/2079-4304.2025.253.341-359

Abstract

The structure and properties of lignin-phenol-formaldehyde resins prepared using technical sodium lignosulfonates were researched. At the first stage, highly alkaline resins were synthesized by replacing up to 40% of phenol with lignosulfonates; at the second stage, medium alkaline resins were synthesized with 30% phenol substituted by lignosulfonates, varying the duration of the polycondensation stage from 15 to 35 min. Based on the results of 13C NMR spectroscopy method it was suggested that highly alkaline resins contain predominantly phenol-formaldehyde oligomers of low molecular weight; the interaction of formaldehyde with lignosulfonates occurs mainly at the first stage of synthesis (at 55–60 °C). Highly alkaline lignin-phenolformaldehyde resins with 20% phenol replaced by lignosulfonates provide the highest physical and mechanical properties among all highly alkaline resins. However, boards manufactured using highly alkaline lignin-phenol-formaldehyde are significantly inferior to boards manufactured using industrial phenol-formaldehyde resin SFZh3014. Reducing the alkali content and increasing the duration of resin holding at 96– 98 °C (second stage) allows to significantly increase the molecular weight of phenolformaldehyde oligomers and improve the properties of lignin-phenol-formaldehyde resins-based particleboard. Phenol-formaldehyde oligomers of medium alkaline resins have a relatively high molecular weight. Particleboards based on medium alkaline resins synthesized with a second stage duration of 25 min meet all the requirements of the state standard. However, boards based on medium alkaline lignin-phenolformaldehyde resins are still inferior to boards based on SFZh-3014.

About the Authors

M. G. Glazunova
St.Petersburg State Forestry University
Russian Federation

GLAZUNOVA Margarita G. – PhD student of the Department of Technology of Wood and Cellulose Composite Materials

194021. Institutskiy per. 5. St. Petersburg



D. V. Ivanov
St.Petersburg State Forest Technical University
Russian Federation

IVANOV Daniil V. – PhD (Technical), Associate Professor of the Department of Wood and Cellulose Composite Materials Technology

194021. Institutskiy per. 5. St. Petersburg

ResearcherID: ABF-7853-2020

SCOPUS Author ID: 57211013094



References

1. Alonso M.V., Oliet M., Rodrı́ guez F., Garcı́ a J., Gilarranz M.A., Rodrı́ guez J.J. Modification of ammonium lignosulfonate by phenolation for use in phenolic resins. Bioresour. Technol., 2005, vol. 96, iss. 9, pp. 1013–1018. DOI: 10.1016/j.biortech.2004.09.009.

2. Aro T., Fatehi P. Production and Application of Lignosulfonates and Sulfonated Lignin. ChemSusChem., 2017, vol. 10, iss. 9, pp. 1861–1877. DOI: 10.1002/cssc.201700082.

3. Christjanson P., Pehk T., Siimer K., Paju J. Structure of polycondensates from hydroxymethylphenols. J. Appl. Polym. Sci., 2007, vol. 107, pp. 1226–1234. DOI: 10.1002/app.27171.

4. Christjanson P., Pehk T., Paju J. Structure and curing mechanism of resol phenol-formaldehyde prepolymer resins. Proc. Estonian Acad. Sci., 2010, vol. 59, pp. 225–232. DOI: 10.3176/proc.2010.3.05.

5. Evstigneyev E.I. Lignin valorization problems. Khimiya Rastitel'nogo Syr'ya, 2022, no. 1, pp. 11–33. DOI: 10.14258/jcprm.2022019211. (In Russ.)

6. Furniture makers restrain price growth. LesPromInform, 2024, vol. 4 (182). URL: https://lesprominform.ru/jarticles.html?id=6733 (accessed January 17, 2025). (In Russ.)

7. Ghorbani M., Konnerth J., van Herwijnen H.W.G., Zinovyev G., Budjav E., Requejo Silva A., Liebner F. Commercial lignosulfonates from different sulfite processes as partial phenol replacement in PF resole resins. J. Appl. Polym. Sci., 2017, vol. 135, iss. 8, art. no. 45893. DOI: 10.1002/app.45893.

8. Gonçalves S., Ferra J., Paiva N., Martins J., Carvalho L.H., Magalhães F.D. Lignosulphonates as an Alternative to Non-Renewable Binders in Wood-Based Materials. Polymers, 2021, vol. 13(23), art. no. 4196. DOI: 10.3390/polym13234196.

9. Kozhevnikov A.Yu., Shestakov S.L., Sypalova Yu.A. Issues of the structural organization of lignin and prospects for its processing. Khimiya Rastitel'nogo Syr'ya, 2023, no. 2, pp. 5–26. DOI: 10.14258/jcrm.20230211737. (In Russ.)

10. Mantanis G.I., Athanassiadou E.Th., Barbu M.C., Wijnendaele K. Adhesive systems used in the European particleboard, MDF and OSB industries. Wood Mater. Sci. Eng., 2017, vol. 13, iss. 2, pp. 104–116. DOI: 10.1080/17480272.2017.1396622.

11. Ogorodnikov S.K. Formaldehyde. Leningrad: Chemistry, 1984. 280 p. (In Russ.)

12. Paju J., Pehk T., Christjanson P. Structure of phenol-formaldehyde polycondensates. Proc. Estonian Acad. Sci., 2009, vol. 58, pp. 45–52. DOI: 10.3176/proc.2009.1.08.

13. Pizzi A., Papadopoulos A.N., Policardi F. Wood Composites and Their Polymer Binders. Polymers, 2020, vol. 15, iss. 5, art. no. 1115. DOI: 10.3390/polym12051115.

14. Vasiliev V.V. Rapid method for determining formaldehyde content in wood boards. Bulletin of the LESTECH Association, 2024, no. 3(17), pp. 32–35. (In Russ.)

15. Zakusilo D.N., Evstigneyev E.I., Ivanov A.Y., Mazur A.S., Bessonova E.A., Mammeri O.A., Vasilyev A.V. Structure of oxidized hydrolysis lignin. J. Wood Chem. Technol., 2023, vol. 43, iss. 2, pp. 103–115. DOI: 10.1080/02773813.2023.2187064.


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For citations:


Glazunova M.G., Ivanov D.V. Effect of alkali content and synthesis duration on the properties of lignin-phenol-formaldehyde resins prepared with technical lignosulfonates. Izvestia Sankt-Peterburgskoj lesotehniceskoj akademii. 2025;(253):341-359. (In Russ.) https://doi.org/10.21266/2079-4304.2025.253.341-359

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ISSN 2079-4304 (Print)
ISSN 2658-5871 (Online)