Lignosulfonate-Based Polyurethane Adhesives

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′-diphenylmethane diisocyanate (pMDI) in the presence or absence of poly(ethylene glycol) with Mw 200 (PEG200) 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 PEG200 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·mol−1.

Alkali-treated wheat gluten cross-linked with sodium alginate as a bio-based wood adhesive for interior grade particleboard

A bio-based wood adhesive formulation free of formaldehyde and made from alkali-treated wheat gluten (WG) and sodium alginate (SA) was developed. Its formulation was optimised, and it was characterised by Fourier Transform Infrared (FT-IR) spectroscopy. The bio-adhesive was utilized to make particleboards both with virgin wood particles and recycled wood particles. A dry bio-adhesive content of 35% (w/w) was used to make samples with both type of particles. Single-layer samples of 10 mm thickness were obtained using wood particles of 1 mm (both virgin and recycled). These samples then were subjected to 3-point bending tests. Whereas the bending strength of samples made with recycled wood particles was 18.09 N/m2 and therefore satisfied Type 18 of the Japanese industrial standards (JIS A 5908:2015), the bending strength of the samples made with virgin wood particles was 8.08 N/m2 and satisfied ‘Type 8 Base particleboard Decorative particleboard’ of the Japanese standards. The density of particleboard samples made from recycled wood particles was 916 kg/m3, while that of samples made from virgin wood particles was 732 kg/m3. The alkali-treated WG and SA bio-adhesive has the potential to be used to re-manufacture particleboards, which can then be recycled and not disposed in landfills.

Keteguhan Rekat Kayu Lapis Sengon Menggunakan Perekat Lignin-Formaldehida dengan Dua Macam Bahan Pengisi (Bonding Strength of Sengon Plywood Using Lignin-Formaldehyde Adhesive with Two Types of Fillers)

Various efforts have been done to reduce the cost, such as finding a suitable mixture of fillers in the adhesive formulation. The aim of this study was to determine the characteristic of lignin-formaldehyde (LF) adhesive and the effect of different content of coconut shell flour and kaolin in the adhesive of lignin on the bonding strength of sengon plywood. Coconut shell flour and kaolin filler content were varied, i.e. 0%, 10%, 20%, 30%, and 40%. The plywood of (20x20x1.5) cm3 size was prepared using a liquid lignin-formaldehyde (LF) with a glue spread of 170 g m-2 surfaces. Bonding strength of plywood was tested to determine the quality of sengon plywood. The results showed that LF adhesive was appeared as a reddish-brown liquid and there were no foreign substances, solid resin content ranges from 31.85 to 35.68%, viscosity of 1.2 poise, acidity (pH) of 11.5, and gelatinized time ranges from 24.20-25.96 minutes. The type and filler content had a significant effect on the bonding strength of sengon plywood. Increasing of the filler content tended to increase the bonding strength of sengon plywood to 30%. The bonding strength of sengon plywood produced using the content of either coconut shell or kaolin flour fillers up to 30% complied with German Standards requirement. The maximum bonding strength value was obtained on adhesives using both types of fillers as much as 10 %.

Peptide Mediated Antimicrobial Dental Adhesive System

The most common cause for dental composite failures is secondary caries due to invasive bacterial colonization of the adhesive/dentin (a/d) interface. Innate material weakness often lead to an insufficient seal between the adhesive and dentin. Consequently, bacterial by-products invade the porous a/d interface leading to material degradation and dental caries. Current approaches to achieve antibacterial properties in these materials continue to raise concerns regarding hypersensitivity and antibiotic resistance. Herein, we have developed a multi-faceted, bio-functionalized approach to overcome the vulnerability of such interfaces. An antimicrobial adhesive formulation was designed using a combination of antimicrobial peptide and a ε-polylysine resin system. Effector molecules boasting innate immunity are brought together with a biopolymer offering a two-fold biomimetic design approach. The selection of ε-polylysine was inspired due to its non-toxic nature and common use as food preservative. Biomolecular characterization and functional activity of our engineered dental adhesive formulation were assessed and the combinatorial formulation demonstrated significant antimicrobial activity against Streptococcus mutans. Our antimicrobial peptide-hydrophilic adhesive hybrid system design offers advanced, biofunctional properties at the critical a/d interface.

Colloidal Lignin Particles as Adhesives for Soft Materials

Lignin has interesting functionalities to be exploited in adhesives for medicine, foods and textiles. Nanoparticles (NPs) < 100 nm coated with poly (L-lysine), PL and poly(L-glutamic acid) PGA were prepared from the laccase treated lignin to coat nanocellulose fibrils (CNF) with heat. NPs ca. 300 nm were prepared, β-casein coated and cross-linked with transglutaminase (Tgase) to agglutinate chamois. Size exclusion chromatography (SEC) and Fourier-transform infrared (FTIR) spectroscopy were used to characterize polymerized lignin, while zeta potential and dynamic light scattering (DLS) to ensure coating of colloidal lignin particles (CLPs). Protein adsorption on lignin was studied by quartz crystal microbalance (QCM). Atomic force microscopy (AFM) was exploited to examine interactions between different polymers and to image NPs with transmission electron microscopy (TEM). Tensile testing showed, when using CLPs for the adhesion, the stress improved ca. 10 and strain ca. 6 times compared to unmodified Kraft. For the β-casein NPs, the values were 20 and 8, respectively, and for the β-casein coated CLPs between these two cases. When NPs were dispersed in adhesive formulation, the increased Young’s moduli confirmed significant improvement in the stiffness of the joints over the adhesive alone. Exploitation of lignin in nanoparticulate morphology is a potential method to prepare bionanomaterials for advanced applications.

Colloidal Lignin Particles as Adhesives for Soft Materials

Lignin has interesting functionalities to be exploited in adhesives for medicine, foods and textiles. Nanoparticles (NPs) &lt;100 nm coated with poly(L-lysine), PL and poly(L-glutamic acid) PGA were prepared from the laccase treated lignin to coat nanocellulose fibrils (CNF) with heat. NPs ca. 300 nm were prepared, &beta;-casein coated and cross-linked with transglutaminase (Tgase) to agglutinate chamois specimens. Size exclusion chromatography (SEC) and Fourier-transform infrared (FTIR) spectroscopy were used to characterize polymerized lignin, zetapotential and dynamic light scattering (DLS) to ensure coating of colloidal lignin particles (CLPs). Protein adsorption on lignin was studied by quartz crystal microbalance (QCM). Atomic force microscopy (AFM) was exploited to examine interactions between different polymers and to image NPs with transmission electron microscopy (TEM). Tensile testing showed, when using CLPs for the adhesion, the stress improved ca. 10 and strain ca. 6 times compared to polymeric lignin. For the &beta;-casein NPs the values were 20 and 8, respectively, and for the &beta;-casein coated CLPs between these two cases. When NPs were dispersed in adhesive formulation, the Young's moduli confirmed significant improvement in the elasticity of the joints over the adhesive alone. Exploitation lignin in nanoparticulate morphology is a potential method to prepare bionanomaterials for advanced applications.