Water Resistance Properties Research Articles

Rigid-Flexible Coupled Dendritic Molecule Doping: General Approach to Activate Commercial Polymers into Harsh Condition-Tolerant Multi-Reusable Strong Supramolecular Adhesives.

Developing functional adhesives combining strong adhesion, good recyclability and diverse harsh-condition adaptability is a grand challenge. Here, we introduce a general dendritic molecule doping strategy to activate commercial polymers into a new family of supramolecular adhesives integrating high adhesion strength, ultralow temperature, water resistant and multi-reusable properties. Our method involves rational design of a new rigid-flexible coupled dendritic molecule-M4C8OH as a versatile dopant, while simple M4C8OH doping into commercial polymers can modulate internal and external non-covalent interaction to enable H-bonding enhanced interchain cross-linking for tough cohesion along with enhanced interphase interaction. This endows 20 wt % M4C8OH-doped polycaprolactone (PCL) adhesives (PCL-M4C8OH) with improved adhesion strength on various substrates with the maximum increase up to 2.87 times that of PCL. In particular, the adhesion strengths of PCL-M4C8OH on polymethyl methacrylate at 25 °C and -196 °C reach 4.67 and 3.58 MPa-1.9 and 2.3 times those of PCL and superior to diverse commercial adhesives and most reported adhesives. PCL-M4C8OH also displays markedly-improved multi-usability and tolerance against ultralow temperature and diverse wet environments. Mechanism studies reveal the crucial role of M4C8OH molecular structures toward superior adhesion. Our method can be expanded to other polymer matrices, yielding diverse new supramolecular adhesives.

A sustainable black liquor-based carbon scavenger to promote urea formaldehyde as green wood adhesive with low formaldehyde emission.

The current study focuses on finding an ecological method to dispose of black liquors (BLs), containing lignin macromolecules, which are produced as byproducts of rice straw-based paper production. In addition to maximizing their value as precursors in the preparation of novel formaldehyde scavengers to avoid the environmental risks associated with using urea formaldehyde in agro-wood composites. To optimize the route, various black liquors are prepared from pulping of rice straw by different pulping agents (alkali, neutral, acidic and kraft reagents) used as additions or precursors for carbon compounds. Elemental analysis, thermogravimetric analysis [TGA], Fourier transform infrared [FTIR] and scanning electron microscope (SEM), are the techniques used to characterize the BLs; while the gel time, bond strength, and differential scanning calorimetry (DSC) methodologies are applied to determine the impact of black liquor (BL) and black liquor‑carbon nanostructures (BL-CNSs) on performance of urea formaldehyde (UF) adhesive. The behavior of the investigated BL-CNSs as HCHO-scavengers is assessed from their affinity to capture the HCHO, and reduction of free-HCHO in UF-palm fibers agro-composites. BL-CNSs, as novel scavengers, exhibit promising properties where the bonding strength of BL-CNSs-UF adhesives increased to 19.7 MPa even though the UF was only 8.4 MPa. Moreover, the formaldehyde adsorption capacity ranges from 35.4 to 63.6 mg/g as well as lowering the gel time. It is interesting to note that the investigated scavengers not only reduced the free-HCHO of composites by about 40-91 %, but also enhancement in their mechanical and water resistance properties; where the modulus of rupture (MOR), internal bond (IB) and reduction in thickness swelling improved to about 50 % and 83.3 %, and 38.8 %, respectively. According to the American National Standards Institute (ANSI) standard these new scavengers, especially from BL of neutral pulping, permit the production of an eco-board (E1) with static bending exceeding the H-3 class.

Optimization of a Low Surface Energy Coating for Enhanced Water Resistance and Condensation Suppression

This study focuses on formulating a low-surface-energy, water-resistant, and anti-condensation coating utilizing a fluorocarbon and acrylic resins composite (FAC), enhanced by six functional additives: antistatic agents, water-repellent agents, nanofillers, anti-mold and anti-algae agent, leveling agents, and wetting and dispersing agents. An orthogonal experimental design was implemented to systematically investigate the effects of varying concentrations of these additives on the surface tension of the coating. The results show that the optimized combination of fluorocarbon and acrylic resins composite (OFAC)with functional additives significantly reduces the surface tension, thereby improving both water resistance and anti-condensation properties. This research advances the development of more efficient surface treatment technologies, particularly for applications requiring enhanced water resistance and anti-condensation performance.

Effect of aminolysis treatment on self-healing properties and printing potentialities of banana peel and edible wax based biodegradable film

Cellulose-based materials are a viable alternative to petroleum-based sources; however, the practical applicability of cellulose films is severely limited by their poor hydrophobicity. This study explores the development of hydrophobic films with self-healing properties through the incorporation of natural wax into a cellulose matrix. Different formulations of films were developed varying the concentration of glycerol (0 % to 3.5 % v/v) and aminolysis treatment. Printability property, rubbing, acid, and water resistance property of the film were also evaluated. The self-healing efficiency of the films varied from around 30 % to 80 % based on variations in glycerol and aminolysis treatment provided. Aminolysis-treated films showed enhanced self-healing properties (Self-healing efficiency ~77 %) compared to the control films. The films were characterized for their physical, mechanical, barrier, and thermal properties and it was found that 1.5 % had superior properties compared to other compositions. Printability properties showed that aminolysis-treated films had better wetting properties (WCA ~ 74.46°) with a peak tact force of 8.1 N. This signifies aminolysis-treated films had better ink absorption and adhesion properties, which confirms the printability nature of the films. This study highlights the potential applications of biodegradable self-healing based film, applications with a scope of resolving environmental problems by replacing petrochemical plastics.

Improved interfacial compatibility between unsaturated polyester resin and rice straw fibers after non-washing treatment with Ca(OH)2

The agricultural industry produces a substantial volume of rice straw (RS) annually, highlighting the importance of recycling RS for sustainable materials. However, the poor interfacial compatibility between RS and polymers often leads to drawbacks in their composites, such as water-swelling and limited tensile strength. Here, we propose a novel approach using Ca(OH)2 that offers several distinct advantages: enhancement of interfacial compatibility, elimination of the need for water washing, and formation of calcified hybrid particles on fiber surfaces by capturing CO2 from the atmosphere. The non-washing calcified rice straw (NCRS) fibers were used to fabricate composites with unsaturated polyester resin (UPR), resulting in NCRS/UPR composites exhibiting significant enhancements in water resistance and mechanical properties compared to RS/UPR composites. The NCRS/UPR composites achieved a water absorption rate below 25 %, thickness swelling rate below 10 %, and tensile strength of 19.9 MPa. This work comprehensively explored the mechanism underlying these achievements through experimental studies. Findings suggest that CaCO3 particles involving with released lignin act as an interfacial bridge between RS fiber surface and UPR, resulting in significantly improved properties. This approach demonstrates promising prospects as a simple and eco-friendly methodology for manufacturing RS-based composite materials.

The preparation and construction of biomimetic mineralization compatible interface of wood fiber/foamed magnesium oxychloride lightweight composites

The purpose of this study is to improve the application performance of foamed magnesium oxychloride cement (FMOC) and solve the problem of poor interfacial compatibility between the organic-inorganic interface of traditional inorganic composite materials. Inspired by the adhesion mechanism of barnacles to inorganic substrates through amyloid nanofibers and phosphoprotein, a simple green method was proposed to improve the strength and water resistance of the system. The FMOC composites (30×30×30 mm) were prepared by adding wood flour (WF) and phytic acid (PA) to the mixture of magnesium oxide and magnesium chloride. The influences of WF and PA on the compressive strength, composition, microstructure, pore structure, water resistance and flame retardant properties of FMOC were investigated. WF was used as a skeleton structure to induce cement particle aggregation, the PA molecule was used as a connecting bridge to activate the fiber skeleton to increase the active sites, and promote crystal nucleation and aggregation through hydrogen and ionic bond interactions to construct the biomimetic mineralized structure. The results show that the introduction of PA improves the compressive strength and water resistance of the FMOC/WF/PA composite system. When the PA addition amount is 0.8 %, the compressive strength of FMOC/WF/PA-0.8 % composites reached 6.64 MPa, which was 3 times compared to the FMOC composites. The softening coefficient and water absorption of the obtained FMOC/WF/PA-0.8 % composites were 0.81 and 13.84 %, respectively, which were superior to FMOC composites and presented better behavior in water resistance. Meanwhile, the modified composites have more stable pore structure and flame retardant properties, thus these green FMOC/WF/PA composites displayed potential application value in building energy conservation, aerospace and other fields.

Enhanced performance of low-dielectric siloxane-polyimide copolymers: Synthesis and properties

Low-dielectric polyimides (PI) films with outstanding overall performance are attractive for next generation microelectronic applications. Herein, a series of two different FPIs and BPIs derived from 4,4′-diaminodiphenyl ether (ODA) and two different functional dianhydrides, 4,4'-(hexafluoroisopropylidene) biphthalic anhydride (6FDA) and 4,4′-(4,4′-isopropyldiphenoxy) biphthalic anhydride (BPADA), respectively, were synthesized by a conventional two-step methodology that included thermoimidatization. Additionally, employing aminopropyl-terminated polydimethylsiloxane PDMS (molecular weight = 1000) as the source of siloxane-oxygen bonds, a series of polyimide siloxane (SiFPIs and SiBPIs) copolymers were synthesized by varying the siloxane content (ranging from 0 to 5 wt%) within the copolymer structure. The effects of siloxane bond on the thermal, solubility, water resistance, dielectric and mechanical properties of polyimide were investigated systematically. The integration of siloxane significantly enhanced the solubility of these copolymers in polar aprotic solvents (DMAC, DMF, NMP), expanding their applicability in diverse processing environments. Crucially, these copolymers exhibited remarkably low dielectric constants—2.90 for SiFPI at 3% PDMS and 2.92 for SiBPI at 4% PDMS—coupled with low loss values, positioning them as prime candidates for advanced microelectronic applications. All the composite films have high thermal stability near pure PI. The introduction of PMDS into PI can improve the elongation at break and at the same time, the composite films still remained with higher modulus and tensile strength. Extensive hydrophobicity assessments through contact angle and water absorption studies underscored the copolymers’ superior moisture resistance, a critical parameter for their potential deployment in high-performance, environmentally sensitive electronic components.

Recycling of collagen from solid tannery waste and prospective utilization as adhesives.

Abstract This study explores the innovative potential of recycled collagen derived from tannery waste for use in high-performance adhesive formulations. The leather industry generates significant amounts of solid waste, primarily from chromium-tanned leather, which poses substantial environmental challenges. Recent advancements in recycling techniques have opened new avenues for repurposing this waste, particularly through collagen extraction, which comprises about 30-35% of tannery residues. This research systematically reviews the methods and applications of collagen extraction, highlighting the material’s versatility and environmental benefits when used as a bio-adhesive. The review identifies key challenges such as low water resistance, shear strength, and adhesiveness in collagen-based adhesives compared to synthetic counterparts. However, innovative solutions are emerging, including the incorporation of silane coupling agents and cross-linking technologies that significantly improve the water resistance and mechanical properties of these adhesives. Economic analyses further support the viability of using tannery waste-derived collagen in adhesive production, aligning with global sustainability goals and reducing reliance on petrochemical-based adhesives. Despite these advancements, the transition from laboratory research to commercial applications remains a significant challenge. Current studies primarily focus on small-scale experiments, with limited pilot-scale studies available. Nonetheless, the potential for collagen-based adhesives to replace harmful chemicals in industrial applications is promising, especially in sectors requiring biodegradable and non-toxic materials. This review concludes that while significant progress has been made, further research is necessary to overcome existing limitations and fully realize the commercial potential of collagen-based adhesives derived from tannery waste.

Preparation and characterization of waterborne silicone modified epoxy resin

AbstractSilicone modified epoxy resin was synthesized with bisphenol‐A epoxy resin (E51) and dimethyldichlorosilane (DMDCS), and waterborne silicone modified epoxy resin (WSER) was prepared. The WSER emulsion exhibited good stability with particle size ranging from 0.5 to 2 μm. Compared with waterborne epoxy resin (WER) cured film, the water resistance of WSER cured film was enhanced by the excellent hydrophobicity of DMDCS. Furthermore, the WSER cured film with 6% DMDCS showed better mechanical properties, and Shore hardness and tensile strength of that were greatly increased. Moreover, the corrosion resistance and ultraviolet (UV) aging resistance of WSER cured film were obviously improved compared to WER cured film.Highlights Dimethyldichlorosilane (DMDCS) was employed to modify bisphenol‐A epoxy resin (E51). Waterborne silicone modified epoxy resin (WSER) was prepared by phase inversion method. WSER cured films did better than WER cured film in water resistance and mechanical properties. WSER cured films showed good corrosion resistance and ultraviolet aging resistance.

Consumers’ perceptions of per- and polyfluoroalkyl substances and bio-based treatments on disposable dinnerware

Per- and polyfluoroalkyl substances (PFAS) are forever chemicals that have been used for their heat, grease, and water-resistant properties on disposable dinnerware. However, PFAS pose risks to human health and the environment and alternative treatments are currently being implemented in the disposable dinnerware industry, including bio- or plant-based treatments. To date, consumer perceptions of the practical usage and environment-related attributes of PFAS versus plant-based alternative treatments have not been addressed. An online survey elicited 1304 U S. consumers' perceptions of the attributes from each treatment and factors impacting those perceptions. On average, participants purchased disposable plates 13 times per year with 50 % ± 50 purchasing them for everyday use. Approximately 20 % ± 40 of the sample had heard of PFAS prior to the study while 62 % ± 49 had heard of bio-based products. In general, PFAS treatments were perceived as performing slightly better in the practical usage attributes (i.e., grease resistant, water resistant, durable); however, the plant-based alternative treatments were perceived as more environmentally friendly (i.e., better for the environment, better for personal health, recyclable, compostable). Older participants viewing plant-based treatments as better at grease resistance, water resistance, durability, and microwavable relative to younger participants. Conversely, people with higher education levels viewed plant-based treatments as less resistant to grease but more durable. Interestingly, participants’ perceptions and existing knowledge of PFAS and bio-based products influenced their perceptions of plant-based treatments being more environmentally friendly. Results provide insights for industry stakeholders as they move forward in implementing PFAS alternative treatments.

Improving Water Resistance and Mechanical Properties of Crosslinked Waterborne Polyurethane Using Glycidyl Carbamate

Waterborne polyurethane (WPU) often suffers from poor water resistance and mechanical properties due to hydrophilic emulsifiers. To address these issues, this study introduces glycidyl carbamate (GC) as a crosslinker to improve WPU performance. Three types of GC were synthesized using aliphatic, cycloaliphatic, and aromatic isocyanates, respectively. The crosslinked network was established through a reaction between the epoxide group of GC and the carboxylic acid and amine groups of WPU. Among these, the WPU film utilizing aromatic isocyanate-based GC exhibited the highest crosslink density, modulus, hardness, and water resistance, due to the rigidity of the aromatic molecular structure. However, the film displayed excessive brittleness, resulting in reduced tensile strength, along with yellowing typically associated with aromatic compounds. The WPU crosslinked with cycloaliphatic GC demonstrated the next best mechanical properties and water resistance, with a 2.7-fold increase in tensile strength, a 1.5-fold increase in hardness, and a 66% reduction in the water swelling ratio compared to neat WPU. This study presents a novel and effective strategy to enhance the water resistance and mechanical properties of WPU films, making them suitable for advanced coating applications.

Development of carboxymethyl cellulose/starch films enriched with ZnO-NPs and anthocyanins for antimicrobial and pH-indicating food packaging

Active packaging, which can monitor food freshness and extend the shelf life, has gained significant attention in recent years. This study aims to develop a novel carboxymethyl cellulose (CMC)/starch/anthocyanins/ZnO active films with enhanced properties and specific functionalities. Scanning electron microscopy (SEM) and X-ray diffraction (XRD) revealed that the addition of anthocyanins and nano-ZnO particles (ZnO-NPs) led to heterogeneous microstructures and a slight decrease in the crystallinity. Fourier transform infrared spectroscopy (FTIR) indicated that there were no chemical interactions among film components. Active films containing ZnO-NPs exhibited improved ductility, as well as enhanced light barrier and water resistance properties. Notably, a shift from hydrophilic to hydrophobic behavior of the films was observed with high ZnO-NP content, as evidenced by a significant increase in the water contact angle (from 63.44° to 114.22°). Furthermore, the presence of only 1 % ZnO-NPs resulted in efficient inhibition of Escherichia coli (E. coli) and Staphylococcus aureus (S. aureus) growth. Moreover, active films containing both anthocyanins and ZnO-NPs were highly sensitive to pH changes in buffer solutions (pH 2–11). Based on the results, a recommended film formulation for future active packaging applications is a 80:20 CMC/starch blend with 3 % ZnO-NPs and 0.1 g anthocyanins.

Tannic acid-modified magnesium oxychloride bone cement with high water resistance and osteogenic properties

Magnesium oxychloride bone cement (MOC) is a bone replacement material that exhibits excellent mechanical properties and is non-toxic. However, the material exhibits poor water resistance, as the 5-phase composition of MOC decomposes readily in the presence of water. Tannic acid (TA) is an organic acid with favorable biocompatibility, containing a large amount of -OH that can form chelates with metal ions. Therefore, we plan to control spill Mg2+ in MOC using TA to improve its water resistance. The results demonstrate that the addition of TA resulted in a denser structure of MOC, an improved stability of the 5-phase in solution, a reduced degradation rate and pH value of MOC in body fluids, and the generation of hydroxyapatite in vitro. Furthermore, the MOC modified with TA demonstrated enhanced cell proliferation and increased new bone formation in cellular and animal experiments. This high-strength, highly bioactive material system is adaptable to patient-specific requirements and has significant potential for clinical translation.

Enhanced mechanical, thermal, water and UV aging resistance properties of bamboo fiber/HDPE composites through silane coupling agent modified nano-SiO2-TiO2

Nano-TiO2 is widely employed to enhance the properties of plant fiber reinforced thermoplastic polymer composites due to its chemical inertness, anti-aging, and anti-bacterial properties. However, the enhancement of bamboo fiber/high-density polyethylene (BF/HDPE) composites is limited by the high photocatalytic activity of nano-TiO2 and its poor compatibility with the BF/HDPE matrix. This study employs an organic-inorganic co-modification to prepare BF/HDPE composites reinforced with silane coupling agent KH550 modified nano-SiO2 coated nano-TiO2 (KH550/SiO2-TiO2) by spray coating and melt mixing methods, and the properties of the composites were tested and characterized. The effects of KH550 and KH550/SiO2-TiO2 content on the properties of modified BF/HDPE composites, including mechanical properties, water absorption, thickness swelling rate, water contact angle, thermal stability, and UV aging resistance，which were characterized using methods of mechanical tests, FTIR, UV-Vis, XPS and SEM, both before and after modification. The results indicate that KH550 effectively improves the agglomeration phenomenon and enhances the dispersibility of nano-SiO2-TiO2 in the BF/HDPE composites. The optimal thermal stability is achieved when the BF/HDPE composites modified with a 5 wt% KH550/SiO2-TiO2, while BF/HDPE composites modified with a 3 wt% KH550/SiO2-TiO2 exhibit the better mechanical properties, water resistance, and UV aging resistance compared to other contents. Flexural strength and modulus of KH550/SiO2-TiO2 modified BF/HDPE composites increased by 18.71 % and 17.92 %, tensile strength and modulus increased by 7.74 % and 21.92 %, respectively. The 480-hour water absorption and thickness swelling rate decreased by 18.68 % and 20.73 %, respectively, and the contact angle increased by 19.17°; better thermal stability and color stability was observed. The spray coating method was more effective in improving the properties of the modified BF/HDPE composites than the melt mixing method. Comprehensive analysis indicates that the mechanical properties, water resistance, thermal stability, and UV aging resistance of the BF/HDPE composites reinforced with 3 wt% KH550/SiO2-TiO2 prepared by the spray coating method are significantly enhanced.

Development of high-quality and water-resistant PBG through H-PDMS modification: From experiments to molecular dynamics simulation

The effective treatment and high-value application of phosphogypsum (PG) are of critical importance for the sustainable development of this construction material. However, its poor water-resistance property has limited its application in the construction field. In order to expand the application potential of phosphorous-building gypsum (PBG) as a durable material, potassium hydroxide (KOH) and hydroxyl‑terminated polydimethylsiloxane (H-PDMS) were used as the activating agent, and the water-resistant modifying agent in this study, respectively, to develop a high-quality and water-resistant PBG product. In addition, molecular dynamics was used to reveal the modification mechanism of H-PDMS and the water-resistance mechanism of KOH activating PBG. The study results show that H-PDMS can significantly improve the water-resistance performance of PBG test blocks. KOH can increase the surface activity of PBG by introducing -OH radicals, promote the reaction between H-PDMS and PBG, and form a dense hydrophobic layer on PBG, thus effectively improving its water-resistance performance. The number of surface active -OH radicals in PBG, the clustering effect of H-PDMS, and impurities in PBG can all result in different experimental and simulation outcomes. Meanwhile, the electrostatic force is an important factor influencing the adsorption of water droplets on the surface of PBG, and the reaction of H-PDMS with PBG normally occurs between Si-O and S-O. This study has systematically interpreted the working mechanism of water-resistant PBG, presenting an important significance in the utilization of PG resources.

Synthesis and characterization of bioplastics based on silyated starch and acrylated epoxidized soybean oil

In the study, the bioplastics were prepared by coupling silylated starch with acrylated epoxidized soybean oil (AESO) at various curing temperatures. 3-aminopropyltriethoxy silane (APTES) was grafted onto starch by the condensation between Si-OH and C-OH. As demonstrated by FTIR and silica content analysis, starch was successfully modified by APTES. The compatibility between silylated starch and AESO was weak as observed by FESEM. The appearance of C-N bonds confirmed the reaction between AESO and silylated starch. An apparent increase of tensile strength from 8.03 MPa to 14.12 MPa was discovered when the bioplastics were cured from 80 °C to 120 °C. Opacity of the bioplastics was enhanced remarkably by AESO due to the incompatibility of silylated starch and AESO. Water resistance test showed that the bioplastics were less sensitive to water after the addition of AESO. The bioplastics maintained good biodegradability after the introduction of AESO. However, increasing the curing temperatures of the bioplastics yielded weak effects on the water resistance and enzymatic degradation of the bioplastics. The bioplastics with excellent mechanical and water-resistant properties were synthesized via the incorporation of AESO under high-temperature curing. The property changes are highly desirable for packaging applications.

Characterization and optimization of desulfurized construction gypsum modified with functionalized nanocellulose

This study focuses on the development and characterization of a novel composite material based on flue gas desulfurization (FGD) gypsum modified with functionalized nanocellulose. The incorporation of 0.1 wt% nanocellulose into the FGD gypsum matrix resulted in significant improvements in mechanical strength, water resistance, and thermal insulation properties. The flexural and compressive strength of the optimized composite increased by 32 % and 27 %, respectively, compared to the control sample. The water absorption decreased by 22 %, and the softening coefficient increased from 0.72 to 0.85, indicating enhanced water resistance. The thermal conductivity of the composite was reduced by 31 %, showcasing its potential as an energy-efficient building material. SEM analysis revealed a refined microstructure with improved interfacial bonding between the nanocellulose and gypsum matrix, while FTIR spectroscopy confirmed the presence of chemical interactions between the components. The moisture buffering capacity of the composite was also superior, with a 38 % higher moisture buffering value than the control sample. These findings highlight the potential of functionalized nanocellulose as a reinforcing agent in FGD gypsum-based composites, offering a promising solution for the development of high-performance, eco-friendly building materials.

Advancing sustainable molded packaging: Integrating silica aerogel into recycled paper pulp for the fabrication of thermally and mechanically stable superhydrophobic composites

In recent years, the growing demand for sustainable packaging has significantly fueled the quest to explore novel approaches that enhance the applicability of renewable alternatives. This study leverages the unique properties of silica aerogel (SA) to address the limitations of traditional molded pulp products. By integrating SA into recycled paper pulp (RP), we aimed to improve water resistance, thermal stability, and mechanical properties. Composites were prepared with varying SA concentrations (1–10 %). Contact angle measurements showed enhanced hydrophobicity, with RP/SA3 % achieving a contact angle of 152.09°, compared to 122.39° for neat RP. The tensile index (TI) of RP/SA composites with 3 % SA increased by 21.09 % compared to neat RP, indicating better mechanical strength. Thermal conductivity significantly decreased, with RP/SA10 % reducing from 0.155 W m−1·K−1 in neat RP to 0.088 W m−1·K−1, a 43.2 % improvement in thermal insulation. Additionally, composites with 1 % and 3 % SA maintained high biodegradability, showing over 50 % degradation after six weeks in soil. These results suggest that incorporating SA into RP composites enhances their functionality without compromising biodegradability, offering a promising solution for sustainable packaging. As regulatory bodies emphasize resource management and waste reduction, the potential of these innovative and environmentally friendly packaging solutions becomes increasingly significant.

Influence of hot-pressing temperature and density on the physical and mechanical properties of bamboo scrimber

Bamboo scrimber (BS) has been widely used as a high-performance engineering composite in construction and outdoor applications, typically employing a thermosetting adhesive that requires hot-pressing. Previous studies have focused on the effects of resin content and BS curing temperature, often overlooking the self-bonding of bamboo during the hot-pressing process. This study investigated the impact of hot-pressing temperature and density on the physical and mechanical properties of BS containing phenol–formaldehyde resin, with a particular focus on regulating BS self-bonding by adjusting these parameters. The study also examined the effects on the chemical composition and pore structure of BS. The results showed that increasing the hot-pressing temperature from 140 to 180 °C broke unstable bonds in the hemicellulose, cellulose, and lignin components of the BS, leading to new crosslinks through dehydration and thermal degradation reactions. This process enhanced self-bonding, improved water resistance, and resulted in different surface colors. Raising the density from 0.9 to 1.3 g/cm3 made the density distribution of BS more uniform and reduced the size and number of internal pores. These characteristics promoted interfacial bonding and impeded water flow through the material, thereby enhancing its water resistance and mechanical properties. This study elucidates the mechanism behind the performance enhancement of BS and offers insights for its low-cost and environmentally friendly production.

Eco-friendly and novel tannin-based wood adhesive enhanced with cellulose nanofibrils grafted by hyperbranched polyamides

Tannin-based adhesives, as a natural biobased adhesive, have the potential to expand their application in wood industry as substitutes for traditional adhesives. In this study, cellulose nanofibrils and hyperbranched polyamides (HBPA) were studied to address the challenges associated with the low crosslinking degree and poor water resistance characteristics of condensed tannin-based wood adhesives. The modification strategy focuses on grafting oxidized cellulose nanofibrils with hyperbranched polyamides through the Schiff base reaction. Comprehensive analyses, including FTIR, XPS, XRD, and TG, confirm the successful binding of oxidized cellulose nanofibrils with hyperbranched polyamides, demonstrating their potential to enhance the properties of tannin adhesives. Furthermore, the investigation about bonding strength, and water resistance of tannin adhesives reveal significant improvements in the mechanical and water resistance properties through this modification strategy. In particular, the maximum wet shear strength is 0.7 MPa, meeting the requirements for Class II plywood. This study provides valuable insights into improving the performance of tannin adhesives, offering promising implications for broader applications and contributing to eco-friendly practices in the wood industry.