期刊
MATERIALS
卷 14, 期 22, 页码 -出版社
MDPI
DOI: 10.3390/ma14227072
关键词
lignosulphonate; adhesive; pMDI; polyurethane; adhesion; curing kinetics; PEG; DSC; ABES
类别
资金
- Portuguese Foundation for Science and Technology (FCT)/Ministry of Science, Technology and Higher Education (MCTES) [UIDB/50011/2020, UIDP/50011/2020]
- Laboratory for Process Engineering, Environment, Biotechnology and Energy-LEPABE - national funds through the FCT/MCTES (PIDDAC) [UIDB/00511/2020]
- FCT
- European Social Fund (ESF) [SFRH/BD/121275/2016]
- Fundação para a Ciência e a Tecnologia [SFRH/BD/121275/2016] Funding Source: FCT
The feasibility of using lignosulfonate from acid sulphite pulping of eucalyptus wood as an unmodified polyol in polyurethane adhesives was evaluated. The addition of poly(ethylene glycol) with M-w 200 (PEG(200)) was found to improve the homogenization of the reaction mixture and enhance adhesive strength.
The feasibility of using lignosulfonate (LS) from acid sulphite pulping of eucalyptus wood as an unmodified polyol in the formulation of polyurethane (PU) adhesives was evaluated. Purified LS was dissolved in water to simulate its concentration in sulphite spent liquor and then reacted with 4,4 & PRIME;-diphenylmethane diisocyanate (pMDI) in the presence or absence of poly(ethylene glycol) with M-w 200 (PEG(200)) as soft crosslinking segment. The ensuing LS-based PU adhesives were characterized by infrared spectroscopy and thermal analysis techniques. The adhesion strength of new adhesives was assessed using Automated Bonding Evaluation System (ABES) employing wood strips as a testing material. The results showed that the addition of PEG(200) contributed positively both to the homogenization of the reaction mixture and better crosslinking of the polymeric network, as well as to the interface interactions and adhesive strength. The latter was comparable to the adhesive strength recorded for a commercial white glue with shear stress values of almost 3 MPa. The optimized LS-based PU adhesive formulation was examined for the curing kinetics following the Kissinger and the Ozawa methods by non-isothermal differential scanning calorimetry, which revealed the curing activation energy of about 70 kJ & BULL;mol(-1).
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