Synthesis and characterization of aminated Lignin-based Hydrogel

Document Type : Research Paper

Authors

1 ....

2 Associate Professor, Department of wood and paper science and technology, faculty of natural resources, university of Tehran, Karaj, Alborz, Iran

3 Associate Prof. at University of Tehran

Abstract

Conversion of renewable and sustainable materials to valuable products is a known way to replace synthetic polymers with natural polymers. lignin is a bio-renewable material and it is the second most abundant biopolymer from biomass. In this work, lignin-based hydrogel was synthesized by crosslinking reactions between dialdehyde cellulose and aminated lignin. Lignin was subjected to amination by Mannich reaction and cellulose was oxidized by sodium metaperiodate, which has been confirmed by FTIR spectroscopy too. The FTIR spectroscopy of the produced hydrogel showed that aldehyde groups of oxidized cellulose react with the amino groups of aminated lignin through a Schiff base, which provide the successfully crosslinking for construction of a hydrogel network. SEM revealed a porous architecture of hydrogel with different pore size distributions. The surface Properties of hydrogel was determined by BET analysis, which indicated the internal porosity of the hydrogel. The results confirmed that the aminated lignin-based hydrogel prepared in this research is a sustainable green hydrogel, which would be beneficial for different applications.
Conversion of renewable and sustainable materials to valuable products is a known way to replace synthetic polymers with natural polymers. Lignin, bio-renewable material, is the second most abundant biopolymer from biomass. In this work, the lignin-based hydrogel was synthesized by crosslinking reactions between dialdehyde cellulose and aminated lignin. So lignin was subjected to amination by Mannich reaction and cellulose was oxidized by sodium metaperiodate, which has been confirmed by FTIR spectroscopy results. The FTIR spectroscopy of the produced hydrogel showed that aldehyde groups of oxidized cellulose react with the amino groups of aminated lignin through a Schiff base, which provides the successful crosslinking for the construction of a hydrogel network. SEM revealed a porous architecture of hydrogel with different pore size distributions. The surface properties of hydrogel were determined by BET analysis, which indicated the internal porosity of the hydrogel. The results confirmed that the aminated lignin-based hydrogel prepared in this research was a sustainable green hydrogel, which would be beneficial for different applications (hygiene, agriculture, etc).

Keywords


[1]   Adebajo, M.O., Frost, R.L., Kloprogge, J.T., Carmody, O. and Kokot, S., 2003. Porous Materials for Oil Spill Cleanup: A Review of Synthesis and Absorbing Properties. Porous Materials, 10: 159-170.
[2]   Nishida, M., Uraki, Y. and Sano, Y., 2003. Lignin gel with unique swelling property. Bioresource Technology, 88: 81-83.
[3]   Quraishi, S., Martins, M., Barros, A., Gurikov, P., Raman, S.P., Smirnova, I., Duarte, A. and Reis, R., 2015. Novel non-cytotoxic alginate–lignin hybrid aerogels as scaffolds for tissue engineering. Supercritical Fluids, 105: 1-8.
[4]   Mahinroosta, M., Farsangi, Z., Allahverdi, A. and Shakoori, Z., 2018. Hydrogels as intelligent materials: A brief review of synthesis, properties and applications. Materials Today Chemistry, 8: 42-55.
[5]   Farhat, W., Venditti, R., Mignard, N., Taha, M., Becquart, F. and Ayoub, A., 2017. Polysaccharides and lignin based hydrogels with potential pharmaceutical use as a drug delivery system produced by a reactive extrusion process. Biological Macromolecules, 104: 564–575.
[6]   Ciolacu, D., Doroftei, F., Cazacu, G. and Cazacu, M., 2013. Morohological and surface aspects of cellulose-lignin hydrogels. Cellulose chemistry and technology, 47: 377-386.
[7]   Sathawong, S., Sridach, W. and Techato, k., 2018. Lignin: Isolation and preparing the lignin based hydrogel. Environmental Chemical Engineering, 6(5): 5655-6760.
[8]   Yu, C., Wang, F., Zhang, C., Fu, S. and Lucia, L., 2016. The synthesis and absorption dynamics of a lignin-based hydrogel for remediation of cationic dye-contaminated effluent. Reactive and Functional Polymer, 106: 137–142.
[9]   Passauer, L., 2012. Highly Swellable Lignin Hydrogels: Novel Materials with Interesting Properties. ACS Symposium Series; American Chemical Society, 1107: 211-228.
[10] Li, X. and Pan, X., 2010. Hydrogels Based on Hemicellulose and Lignin from Lignocellulose Biorefinery: A Mini-Review. Biobased Materials and Bioenergy, 4: 289-297.
[11] Thakur, S., Sharma, B., Verma, A., Chaudhary, J., Tamulevicius, S. and Thakur, V., 2018. Recent progress in sodium alginate based sustainable hydrogels for environmental applications. Cleaner Production, 198: 143-159.
[12] Sathawong, S., Sridach, W. and Techato, k., 2018. Recovery of Kraft Lignin from OPEFB and Using for Lignin–Agarose Hydrogel. Polymers and the Environment, 26: 3307–3315.
[13] Jiang, X., Yang, Z., Peng, Y., Han, B., Li, Z., Li, X. and Liu, W., 2016. Preparation, characterization and feasibility study of dialdehyde carboxymethyl cellulose as a novel crosslinking reagent. Carbohydrate Polymers, 137: 632-641.
[14] Lucia, A., Bacher, M., Herwijnen, H. and Rosenau, T., 2020. A Direct Silanization Protocol for Dialdehyde Cellulose. Molecules, 25(2458): 1-12.
[15] Wang, M., Sjöholm, E. and Li, J., 2017. Fast and reliable quantification of lignin reactivity via reaction with dimethylamine and formaldehyde (Mannich reaction). Holzforschung, 71(1): 27-34.
[16] Xu, C., Zhan, W., Mo, X., Fu, L. and Lin, B., 2018. Self-healing chitosan/vanillin hydrogels based on Schiff-base bond/ hydrogen bond hybrid linkages. Polymer Testing, 66: 155-163.
[17] Isobe, N., Lee, D., Kwon, Y., Kimura, S., Kuga, S., Wada, M. and Kim, U., 2011. Immobilization of protein on cellulose hydrogel. Cellulose, 18: 1251-1256.
[18] Domínguez-Robles, J., Peresin, M., Tamminen, T., Rodríguez, A., Larrañeta, E. and Jääskeläinen, A., 2018. Lignin-based hydrogels with “super-swelling” capacities for dye removal. Biological Macromolecules, 115: 1249–1259.