Scalable Manufacturing of Environmentally Stable All-Solid-State Plant Protein-Based Supercapacitors with Optimal Balance of Capacitive Performance and Mechanically Robust.

The development of advanced biomaterial with mechanically robust and high energy density is critical for flexible electronics, such as batteries and supercapacitors. Plant proteins are ideal candidates for making flexible electronics due to their renewable and eco-friendly natures. However, due to the weak intermolecular interactions and abundant hydrophilic groups of protein chains, the mechanical properties of protein-based materials, especially in bulk materials, are largely constrained, which hinders their performance in practical applications. Here, a green and scalable method is shown for the fabrication of advanced film biomaterials with high mechanical strength (36.3 MPa), toughness (21.25 MJ m-3 ), and extraordinary fatigue-resistance (213 000 times) by incorporating tailor-made core-double-shell structured nanoparticles. Subsequently, the film biomaterials combine to construct an ordered, dense bulk material by stacking-up and hot-pressing techniques. Surprisingly, the solid-state supercapacitor based on compacted bulk material shows an ultrahigh energy density of 25.8 Wh kg-1 , which is much higher than those previously reported advanced materials. Notably, the bulk material also demonstrates long-term cycling stability, which can be maintained under ambient condition or immersed in H2 SO4 electrolyte for more than 120 days. Thus, this research improves the competitiveness of protein-based materials for real-world applications such as flexible electronics and solid-state supercapacitors.

Nacre-Inspired Strong and Multifunctional Soy Protein-Based Nanocomposite Materials for Easy Heat-Dissipative Mobile Phone Shell.

Inspired by the hierarchically ordered "brick and mortar" (BM) architecture of natural nacre, in this study a rational assembly of boron nitride (BN) nanosheets was introduced into a mixture of trimethylolpropane triglycidyl ether (TTE) and soy protein isolate (SPI), and a strong and multifunctional SPI-based nanocomposite film with multinetwork structure was synthesized. At a low BN loading (<0.5%), the resulting multifunctional film was flexible, antiultraviolet, and nearly transparent and also displayed good thermal diffusion ability and exhibited an excellent combination of high tensile strength (36.4 MPa) and thermal conductivity (TC, 2.40 W·m-1·K-1), surpassing the performances of various types of petroleum-based plastics (displayed a tensile strength ranging from 1.9 to 21 MPa and TC ranging from 0.55-2.13 W·m-1·K-1), including nine different types of materials currently utilized for mobile phone shells, suggesting its vast potential in practical applications.

Pecan Shell-Derived Activated Carbon for High-Electrochemical Performance Supercapacitor Electrode.

Carbon nanomaterials-based electric double-layer capacitors (EDLCs) are reliable and appealing energy-storage systems offering high power density and long cycling stability. However, these energy storage devices are plagued with critical shortcomings, such as low specific capacitance, inefficient physical/chemical activation process, and self-discharge of electrode materials, hindering their future application. In this work, we use a self-activation process, an environmentally benign and low-cost process, to produce high-performance activated carbon (AC). Novel activated carbon from pecan shells (PS) was successfully synthesized through a single-step self-activation process, which combines the carbonization and activation processes. The as-synthesized pecan shell-derived activated carbon (PSAC) provides a high-porosity, low-resistance, and ordered pore structure with a specific pore volume of 0.744 cm3/g and BET surface area of 1554 m2/g. The supercapacitors fabricated from PSAC demonstrate a specific capacitance of 269 F/g at 2 A/g, excellent cycling stability over 15,000 cycles, and energy and power density of 37.4 Wh/kg and of 2.1 kW/kg, respectively. It is believed that the high-efficiency PSAC synthesized from the novel self-activation method could provide a practical route to environmentally friendly and easily scalable supercapacitors.

Programmable and Shape-Color Synchronous Dual-Response Wood with Thermal Stimulus.

Stimuli-responsive materials exhibit huge potential in sensors, actuators, and electronics; however, their further development for reinforcement, visualization, and biomass-incorporation remains challenging. Herein, based on the impregnation of thermochromic microcapsule (TCM)-doped dynamic covalent vitrimers, a programmable shape-color dual-responsive wood (SRW-TC) was demonstrated with robust anisotropic structures and exchangeable covalent adaptable networks. Under mild conditions, the resultant SRW-TC displays feasible shape memorability and programmability, resulting from the rigidity-flexibility shift induced by the glass-transition temperature (34.99 °C) and transesterification reaction triggered by the topology freezing transition temperature (149.62 °C). Furthermore, the obtained SRW-TC possesses satisfactory mechanical performance (tensile strength of 45.70 MPa), thermal insulation (thermal conductivity of 0.27 W/m K), anisotropic light management, and benign optical properties (transmittance of 51.73% and haze of 99.67% at 800 nm). Importantly, the incorporation of compatible TCM enables SRW-TC to visualize shape memory feasibility and rigidity/flexibility switching and respond to the external thermal stimulus through the thermal-induced shape-color synchronous dual-responsiveness, which successfully demonstrates the applications of sensing temperature, grasping objects, encrypting/decoding icon messages, and so on. The proposed facile and highly effective strategy could serve as a guideline for developing high-performance multifunctional wood composite with promising intelligent applications in performance visualization, environmental sensing, materials interactivity, information dual-encryption, local precision shape and color regulation, etc.

A strong and tough supramolecular assembled ß-cyclodextrin and chitin nanocrystals protein adhesive: Synthesis, characterization, bonding performance on three-layer plywood.

The development of a biomass adhesive as a substitute for petroleum-derived adhesives has been considered a viable option. However, achieving both superior bonding strength and toughness in biomass adhesives remains a significant challenge. Inspired by the human skeletal muscles structure, this study reveals a promising supramolecular structure using tannin acid (TA) functionalized poly-ß-cyclodextrin (PCD) (TA@PCD) as elastic tissues and chitin nanocrystals (ChNCs) as green reinforcements to strengthen the soybean meal (SM) adhesive crosslinking network. TA@PCD acts as a dynamic crosslinker that facilitates reversible host-guest interactions, hydrogen bonds, and electrostatic interactions between adjacent stiff ChNCs and SM matrix, resulting in satisfactory strength and toughness. The resulting SM/TA@PCD/ChNCs-2 adhesive has demonstrated satisfactory wet and dry shear strength (1.25 MPa and 2.57 MPa, respectively), toughness (0.69 J), and long-term solvents resistance (80 d). Furthermore, the adhesive can exhibit desirable antimildew characteristics owing to the phenol hydroxyl groups of TA and amino groups of ChNCs. This work showcases an effective supramolecular chemistry strategy for fabricating high-performance biomass adhesives with great potential for practical applications.

Guar gum, a low-cost sustainable biopolymer, for wastewater treatment: A review.

Rapid population growth and the resultant pollution of freshwater resources have created a water stress condition reducing the availability of safe and affordable water. Guar gum, a biocompatible macromolecule obtained from the endosperm of the seeds of Cyamopsis tetragonolobus, is a fascinating raw material for multifunctional adsorbents. This review assembled the work conducted by various researchers over the past few decades and discussed the structure, properties, and different modifications methods employed to develop versatile guar gum-based adsorbent. The paper also summarized the recent progress of guar gum-based nanocomposites for the remediation of multiple hazardous substances such as organic dyes, toxic heavy metal ions, oil-water separation as well as inhibiting the growth of bacterial pathogens. Thus, the important contribution of guar gum composites to safeguard the water quality is highlighted which will overcome the limitations and streamline the future course of innovative research.

The potential of self-activated carbon for adsorptive removal of toxic phenoxyacetic acid herbicide from water.

Phenoxyacetic acid herbicides are widely used in agriculture for controlling weeds. These organic compounds are persistent and recalcitrant, often contaminating water and soil. Therefore, we studied five pristine biochars (BCs), and southern yellow pine (SYP) based self-activated carbon (SAC) for the adsorptive removal of 2,4-Dichlorophenoxyacetic acid (2,4-D) herbicide. Among the tested adsorbents, SYP-SAC-15 demonstrated higher (>90%) 2,4-D removal from water. The SYP-SAC-15 was produced using a facile and green route where the biomass pyrolysis gases worked as activating agents creating a highly porous structure with a surface area of 1499.79 m2/g. Different adsorption kinetics and isotherm models were assessed for 2,4-D adsorption on SYP-SAC-15, where the data fitted best to pseudo-second order (R2 > 0.999) and Langmuir (R2 > 0.991) models, respectively. Consequently, the adsorption process was mainly dominated by the chemisorption mechanism with monolayer coverage of SYP-SAC-15 surface with 2,4-D molecules. At the optimum pH of 2, the maximum 2,4-D adsorption capacity of SYP-SAC-15 reached 471.70 mg/g. Furthermore, an increase in the water salinity demonstrated a positive influence on 2,4-D adsorption, whereas humic acid (HA) showed a negative impact on 2,4-D adsorption. The regeneration ability of SYP-SAC-15 showed excellent performance by retaining 71.09% adsorption capability at the seventh adsorption-desorption cycle. Based on the operating pH, surface area, spectroscopic data, kinetics, and isotherm modeling, the adsorption mechanism was speculated. The 2,4-D adsorption on SYP-SAC-15 was mainly governed by pore filling, electrostatic interactions, hydrogen bonding, hydrophobic and π-π interactions.

Bioinspired Synthesis of Silver Nanoparticles for the Remediation of Toxic Pollutants and Enhanced Antibacterial Activity.

This research presents a novel and environmentally friendly approach for the synthesis of multifunctional nanobiocomposites for the efficient removal of toxic heavy metal and dye, as well as the disinfection of wastewater microorganisms. The nanobiocomposites (KAC-CS-AgNPs) were prepared by incorporating photochemically generated silver nanoparticles (AgNPs) within a chitosan (CS)-modified, high-surface-area activated carbon derived from kenaf (KAC), using a unique self-activation method. The even distribution of AgNPs was visible in the scanning electron microscopy images and a Fourier transform infra red study demonstrated major absorption peaks. The experimental results revealed that KA-CS-AgNPs exhibited exceptional adsorption efficiency for copper (Cu2+), lead (Pb2+), and Congo Red dye (CR), and showed potent antibacterial activity against Staphylococcus aureus and Escherichia coli. The maximum adsorption capacity (mg g-1) of KAC-CS-AgNPs was 71.5 for Cu2+, 72.3 for Pb2+, and 75.9 for CR, and the adsorption phenomena followed on the Freundlich and Langmuir isotherm models and the second-order kinetic model (R2 > 0.99). KAC-CS-AgNPs also exhibited excellent reusability of up to four consecutive cycles with minor losses in adsorption ability. The thermodynamic parameters indicated that the adsorption process was spontaneous and endothermic in nature. The bacterial inactivation tests demonstrated that KAC-CS-AgNPs had a strong bactericidal effect on both E. coli and S. aureus, with MIC calculated for E. coli and S. aureus as 32 µg mL-1 and 44 µg mL-1, respectively. The synthesized bioinspired nanocomposite KAC-CS-AgNPs could be an innovative solution for effective and sustainable wastewater treatment and has great potential for commercial applications.

Oyster-inspired carbon dots-functionalized silica and dialdehyde chitosan to fabricate a soy protein adhesive with high strength, mildew resistance, and long-term water resistance.

Developing multifunctional adhesives with exceptional cold-pressing strength, water resistance, toughness, and mildew resistance remains challenging. Herein, inspired by oysters, a multifunctional organic-inorganic hybrid soybean meal (SM)-based adhesive was fabricated by incorporating amino-modified carbon dots functionalized silica nanoparticles (CDs@SiO2) and dialdehyde chitosan (DCS) into SM matrix. DCS effectively enhanced the interface interactions of organic-inorganic phases and the rigid nanofillers CDs@SiO2 uniformly dispersed in the SM matrix, which provided energy dissipation to improve the adhesive's toughness. Owing to the stiff skeleton structure and enhanced crosslinking density, the crosslinker-modified SM (MSM)/DCS/CDs@SiO2-2 wood adhesive exhibited outstanding cold-pressing strength (0.74 MPa), wet shear strength (1.36 MPa), and long-term water resistance (49 d). Additionally, the resultant adhesive showed superior antimildew and antibacterial properties benefiting from the introduction of DCS. Intriguingly, the fluorescent properties endowed by carbon dots further broadened the application of adhesives for realizing security testing. This study opens a new pathway for the synthesis of multifunctional biomass adhesives in industrial and household applications.

Achieving strong, stable, and durable underwater adhesives based on a simple and generic amino-acid-resembling design.

Developing underwater adhesives is important in many applications. Despite extensive progress, achieving strong, stable, and durable underwater adhesion via a simple and effective way is still challenging, mainly due to the conflict between the interfacial and bulk properties. Here, we report a unique bio-inspired strategy to facilely construct superior underwater adhesives with desirable interfacial and bulk properties. For adhesive design, a hydrophilic backbone is utilized to quickly absorb water for effective dehydration, and a novel amino acid-resembling functional block is developed to provide versatile molecular interactions for high interfacial adhesion. Moreover, the conjunction of these two components enables the generation of abundant covalent crosslinks for robust bulk cohesion. Such a rational design allows the adhesive to present a boosted underwater adhesion (3.92 MPa to glass), remarkable durability (maintaining high strength after one month), and good stability in various harsh environments (pH, salt, high temperature, and organic solvents). This strategy is generic, allowing the derivation of more similar adhesive designs easily and triggering new thinking for designing bio-inspired adhesives and beyond.

Biomimetic lignin-protein adhesive with dynamic covalent/hydrogen hybrid networks enables high bonding performance and wood-based panel recycling.

Exploring the reusability of wood-based panels is imperative in the wood industry for sustainable development and carbon balance. Non-reusable adhesives make wood-based panel recycling difficult. In this study, inspired by the adhesion and de-adhesion behavior of snail slime, we built dynamic covalent/hydrogen hybrid networks into adhesive system for achieving both high bonding performance and reusability. Specifically, the softwood lignin was purified and pretreated by ultrasonication to form a catechol structure (UAL) and then combined with soybean protein to develop a 100 % bio-based wood adhesive. The catechol structure of UAL formed dynamic covalent bonds (CN) with the amino groups of the protein to improve the water resistance and formed multiple hydrogen bonds as a sacrificial network to improve the toughness of the adhesive. Thus, the wet shear strength of plywood bonded by the resultant adhesive improved by 101.4 % to 1.37 MPa. The adhesive also exhibited flame retardancy (LOI = 37.7 %), mildew resistance (60 h), and antibacterial performance (inhibition zone = 8 mm). Notably, owing to the rearrangement of dynamic covalent/hydrogen hybrid networks and the thermoplastic property of UAL, the resultant adhesive was reusable (3 cycles) and degradable (2 months), which provides a potential method for the reuse of wood-based panels.

Lignocellulosic-Based Activated Carbon-Loaded Silver Nanoparticles and Chitosan for Efficient Removal of Cadmium and Optimization Using Response Surface Methodology.

The cadmium-contaminated water body is a worldwide concern for the environment and toxic to human beings and the removal of cadmium ions from drinking and groundwater sustainably and cost-effectively is important. A novel nano-biocomposite was obtained by impregnating silver nanoparticles (AgNPs) within kenaf-based activated carbon (KAC) in the presence of chitosan matrix (CS) by a simple, facile photoirradiation method. The nano-biocomposite (CS-KAC-Ag) was characterized by an environmental scanning electron microscope equipped with energy dispersive X-ray spectroscopy (ESEM-EDX), Fourier-transform infrared spectroscopy (FTIR), and Brunauer−Emmett−Teller (BET) method. A Box−Behnken design of response surface methodology (RSM) was used to optimize the adsorption of Cd2+. It was found that 95.1% of Cd2+ (10 mg L−1) was eliminated at pH 9, contact time of 120 min, and adsorbent dosage of 20 mg, respectively. The adsorption of Cd2+ by CS-KAC-Ag is also in agreement with the pseudo-second-order kinetic model with an R2 (coefficient of determination) factor greater than 99%. The lab data were also corroborated by tests conducted using water samples collected from mining sites in Mexico. Along with Cd2+, the CS-KAC-Ag exhibited superior removal efficiency towards Cr6+ (91.7%) > Ni2+ (84.4%) > Co2+ (80.5%) at pH 6.5 and 0.2 g L−1 dose of the nano-adsorbent. Moreover, the adsorbent was regenerated, and the adsorption capacity remained unaltered after five successive cycles. The results showed that synthesized CS-KAC-Ag was a biocompatible and versatile porous filtering material for the decontamination of different toxic metal ions.

Preparation of a high bonding performance soybean protein-based adhesive with low crosslinker addition via microwave chemistry.

Human health and environmental protection demand wood-based panel industry for innovative soy-based adhesives with high production efficiency, straightforward synthesis processes, non-toxicity, and high bonding performance. A simple and efficient microwave pretreatment process and low addition of bio-derived crosslinking agent was used in this study to prepare a non-toxic and high-bonding performance soybean protein-based adhesive. After 4 min of microwave pretreatment time, the complex quaternary structure of soybean protein molecule unfolds, the soybean protein disperses evenly and stably, and active groups of soybean protein molecules are exposed. After adding 3.85% crosslinking agent, the moisture absorption rate of the soybean protein-based adhesive decreases by 41.77%, the residual rate increases by 3.68%, and the wet shear strength of the resultant plywood increases to 1.12 MPa, which satisfies requirement of interior use plywood. Compared with previously reported soy-based adhesives, this adhesive is dependent on fewer chemical reagents, but has good bonding performance. The 204.41% of relative cell viability indicates the resultant adhesive was non-toxic. The proposed high-efficiency, high-performance, non-toxic biomass adhesive has great prospects for the industrial application.

Bioinspired phenol-amine chemistry for developing bioadhesives based on biomineralized cellulose nanocrystals.

Inspired by the phenol-amine chemistry and biomineralization of insect cuticles, we developed a green and facile strategy for preparing a bio-adhesive with excellent adhesion properties, mildew resistance, and antibacterial activity. This biomimetic strategy incorporates functional catechol-modified ε-polylysine and vanillin via grafting and Schiff base reactions. The biomineralized cellulose nanocrystals were prepared using a cellulose nanocrystal bio-template by regulating the in-situ biomineralization of inorganic nanoparticles, thereby building an optimized organic-inorganic mineralization framework in the polymer. The bonding strength of composite adhesive was significantly improved by multiple cross-linking networks through sacrificial hydrogen bonds, electrostatic interactions, and dynamic covalent bonds. The adhesion strength of the composite adhesive reached 1.13 MPa, which was 151% higher than the pristine adhesive. As a result of the synergistic effect of the catechol component, cationic ε-polylysine, and aldehyde group, the bio-adhesive also exhibited favorable anti-mildew and anti-bacterial properties.

Optically Transparent Bamboo with High Strength and Low Thermal Conductivity.

The objective of this study is to convert bamboo into a transparent material with great optical transmittance and good strength. Bamboo has a much faster regeneration rate than wood, but its high density and high extractive content make it challenging to produce transparent products. This study presents a simple and effective approach that could address this challenge. Pretreatment of bamboo with low concentration sodium hydroxide greatly improved the preparation efficiency of transparent bamboo. The transparent bamboo with a thickness of 1 mm and cellulose volume fraction of 22% made from the pretreated bamboo exhibited an improved total optical transmissivity up to 80%, which was 60% higher than that of untreated bamboo. Compared to transparent wood (TW), although the transmissivity of transparent bamboo was slightly lower, its mechanical strength was almost doubled. Besides, the developed transparent bamboo exhibited a low heat conductivity of 0.203 W m-1 K-1, being about 10% lower than that of TW (0.225 W m-1 K-1) and approximately 80% lower than that of common glass material (0.974 W m-1 K-1). The transparent bamboo would significantly enhance energy-saving performance, being a promising alternative to traditional glass.

Mesoporous activated carbon as a green adsorbent for the removal of heavy metals and Congo red: Characterization, adsorption kinetics, and isotherm studies.

In this study, an effective and green adsorbent was prepared by the self- activation of kenaf fiber and then the kenaf-based activated carbon (KAC) was applied for the removal of lead Pb(II), copper Cu(II), and Congo red (CR) dye from an aqueous solution by the process of adsorption. The surface morphology of mesoporous adsorbent was characterized. The KAC showed good capacity of adsorption of as Pb(II), Cu(II), and anionic dye CR in very short period of agitation. The adsorbent efficiency of metal ions and dye was estimated by varying the adsorbent dose, pH, contact time, initial metals and dye concentration, and temperature. Optimum adsorption of metal ions and CR dye was observed at pH 6, and at pH 4 at 120 min, respectively. The adsorption isotherm was described by the Langmuir and Freundlich isotherm equations. The green adsorbent followed the pseudo-second-order kinetic model with correlation coefficients R2 value >0.99. The increase in adsorption temperature enhanced the adsorption efficiency for both heavy metals and dye. The KAC showed no significant loss of the adsorption capacity after 3 cycles of reuse.

"Green" Flexible Electronics: Biodegradable and Mechanically Strong Soy Protein-Based Nanocomposite Films for Human Motion Monitoring.

Soy protein isolate (SPI) is envisioned as a promising alternative to fabricate "green" flexible electronics, showing great potential in the field of flexible wearable electronics. However, it is challenging to simultaneously achieve conductive film-based human motion-monitoring strain sensors with reliable fatigue resistance, robust mechanical property, environmental degradability, and sensing capability of human motions. Herein, we prepared a series of SPI-based nanocomposite films by embedding a surface-hydroxylated high-dielectric constant inorganic filler, BaTiO3, (HBT) as interspersed nanoparticles into a biodegradable SPI substrate. In particular, the fabricated film comprising 0.5 wt % HBT and glycerin (GL), namely, SPI-HBT0.5-GL0.5, presents multifunctional properties, including a combination of excellent toughness, tensile strength, conductivity, translucence, recyclability, and excellent thermal stability. Meanwhile, this multifunctional film could be simply degraded in phosphate buffered saline solution and does not cause any pollution to the environment. Attractively, wearable sensors prepared with this particular material (SPI-HBT0.5-GL0.5) displayed excellent biocompatibility, prevented the occurrence of an immune response, and could accurately monitor various types of human joint motions and successfully remain operable after 10,000 cycles. These properties make the developed SPI-based film a great candidate in formulating biobased and multifunctional wearable electronics.

Sandcastle worm-inspired phytic acid and magnesium oxychloride cement copolymerization for performance enhancement.

The development of magnesium oxychloride cement (MOC) can convert wastes in the potash industry into valuable products and reduce CO2 emission. The use of acid radicals has the potential to enhance the water resistance of MOC. However, because of the internal stress formed during the crystallization process, the occurrence of cracks accompanied by a significant decrease in the mechanical properties is inevitable. Inspired by the sandcastle worm and organic-inorganic copolymerization, a novel strategy was proposed, which employed phytic acid (PA) to copolymerize with phase 5 crystals to reduce the internal stress and prevent crack generation. XPS and TG-DSC analyses revealed that organic-inorganic copolymers were successfully produced. Furthermore, the compressive strength (CS) and water resistance of MOC-PA were significantly enhanced. The enhanced properties were associated with the coordination bonds and high tension of the rigid rings in phytic acid, which was sufficient to overcome the internal stress. Additionally, the repeated hydrolysis of rod-like phase 5 generated a gel-like phase from the outside inward, enhancing their water resistance. Compared with MOC-0, MOC-0.6 showed a 17.8% increase in CS and a 102.3% increase in water resistance. The microscopic mechanisms of the enhanced CS and water resistance of high-performance greener cements were proposed.

Lightweight, strong, moldable wood via cell wall engineering as a sustainable structural material.

Wood is a sustainable structural material, but it cannot be easily shaped while maintaining its mechanical properties. We report a processing strategy that uses cell wall engineering to shape flat sheets of hardwood into versatile three-dimensional (3D) structures. After breaking down wood's lignin component and closing the vessels and fibers by evaporating water, we partially re-swell the wood in a rapid water-shock process that selectively opens the vessels. This forms a distinct wrinkled cell wall structure that allows the material to be folded and molded into desired shapes. The resulting 3D-molded wood is six times stronger than the starting wood and comparable to widely used lightweight materials such as aluminum alloys. This approach widens wood's potential as a structural material, with lower environmental impact for buildings and transportation applications.

A Tough and Mildew-Proof Soybean-Based Adhesive Inspired by Mussel and Algae.

Despite the recent advances in protein-based adhesives, achieving strong adhesion and mold resistance in wet environment is challenging. Herein, a facile fabrication technology of preparing tough bio-adhesive by incorporating soybean meal and blood meal is presented. Inspired by the marine mussel byssi and brown algae, metal coordination was introduced into a loosely bound protein system to construct multiple chemical cross-linking networks. Mixed alkali-modified blood meal (mBM) was mixed with soybean meal, then 1,6-hexane dioldiglycidyl ether (HDE) and zinc ion were introduced to fabricate soybean meal and blood meal-based adhesives. The attained adhesives exhibited good thermal stability, water resistance (the wet shear strength is 1.1 MPa), and mold resistance, with appropriate solid content (34.3%) and relatively low moisture uptake (11.9%). These outstanding performances would be attributed to the reaction of 1,6-hexane dioldiglycidyl ether with protein to form a preliminary cross-linking network; subsequently, the coordination of zinc ions with amino or carboxyl strengthened and toughened the adhesive. Finally, the calcium ions gelled the adhesives, providing cohesion force and making the network structure more compact. This study realized the value-added utilization of protein co-products and developed a new eco-friendly bio-based adhesive.