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The thermal decomposition characteristics of microwave liquefied rape straw residues with respect to liquefaction condition and pyrolysis conversion were investigated using a thermogravimetric (TG) analyzer at the heating rates of 5, 20, 50 °C min−1. The hemicellulose decomposition peak was absent at the derivative thermogravimetric analysis (DTG) curve of liquefied residues, because it had been decomposed during the liquefaction. Furthermore, among the liquefied residues, the one from the reaction condition of 180 °C/15 min had the highest thermal stability under a high temperature (>700 °C). The DTG profiles revealed that raising the temperature heating rate could result in an increase in the maximum decomposition temperature. The apparent activation energy (Eα) values of the liquefied residues were lower than that of non-liquefied raw rape straw, whereas the recondensation reaction occurred at 180 °C/15 min remarkably increased the Eα. A noticeable increase in the Eα was observed for the liquefied residue from the 180 °C/10 min samples as the pyrolysis conversion increased from 0.15 to 0.55, suggesting a complex decomposition process with the increasing pyrolysis temperature. The liquefaction process could decrease the thermal decomposition temperature of biomass, which means higher reactivity and lower operational costs during pyrolysis. [ABSTRACT FROM AUTHOR]

In this work, both the bio-polyol and cellulose nanocrystals (CNCs) used to produce high bio-content polyurethane (PU) foams were prepared from microwave liquefaction of rape straw. As high as 40% petro-based polyol was replaced by bio-polyol and the bio-foams containing 40% bio-polyol (PU40) were further reinforced by incorporating 1 to 6% CNCs. GC–MS, 1 H NMR and FTIR observations demonstrated that the bio-polyol is a hydroxyl-rich source consisting of C5, C6 sugars and aromatics. The maximum physico-mechanical performance of bio-foam without CNCs was observed from the bio-foam containing 20% bio-polyol. When further increasing bio-polyol content from 20 to 40%, these properties dramatically decreased. This result was possibly due to the complex polyurethane crosslinking reactions with C5, C6 sugars and aromatics. As compared with reference (PU40), the Young's modulus and compressive stress in the optimal 4% CNCs reinforced bio-foam increased by 590% and 150%, respectively. It was noteworthy that these values were highly superior to those of the petro-based foam. Solid state 13 C NMR and FTIR analysis of CNC reinforced bio-foam evidenced that the hydroxyl-rich structure in CNCs participated in the cross-linking reactions, resulting in an increase of the polyurethane crosslinking density, which contributes to the increased physico-mechanical performance of bio-foam. [ABSTRACT FROM AUTHOR]

Microwave-assisted liquefaction of rape straw in methanol was conducted to collect the liquefied residues for the extraction of cellulose nanocrystals (CNCs). The liquefied residue with content of 23.44% from 180°C/7.5 min was used to fibrillate CNCs with dilute alkali (2% NaOH) and hydrogen peroxide (5% H2O2) treatments, followed by ultrasonication for 15 min. The FT-IR spectra and SEM images revealed that the liquefied residue from 180°C/7.5 min exhibited a relatively homogeneous texture and a huge surface with cellulose as core structure. The retained hemicelluloses and other impurities in the liquefied residue were eliminated by 2% NaOH treatment, and the surface and accessibility of the alkali treated sample were significantly increased by 5% H2O2 treatment. The TEM images confirmed the CNCs had an average diameter of 12.59 nm. The CNCs had good thermal stability with a maximum weight loss temperature of 376.5°C. [ABSTRACT FROM AUTHOR]

Filament fused fabrication (FFF) is an extrusion-based 3D printing technology for manufacturing thermoplastic components. One major obstacle facing 3D printed thermoplastic material is the reduced crystallinity resulting from a fast quench when material exiting the 3D printer hot nozzle solidifies quickly at the low-temperature platform, leading to weak mechanical performance. Here, we report an accelerated annealing strategy with the assistance of microwave heating, aiming to enhance crystallinity and mechanical performance of FFF 3D printed polylactic acid (PLA) composite. We selected naturally abundant cellulose fibers as precursors for producing carbonized cellulose nanofibers (CCNFs), and compounded CCNFs with PLA to produce bi-component filament for 3D printing final composite. After being irradiated with microwave, the embedded CCNFs in composite selectively absorbed microwave energy and generated heat. Subsequently, the localized heat transferred to the adjacent PLA regions, triggering amorphous PLA chains to repack and convert to new crystallites. In this work, annealing conditions, including heating method (i.e., oven annealing vs. microwave annealing), time (0–120 min), and temperature (80 vs. 120 °C), were systematically studied to understand the relevant effects on the resulting parameters including composite crystallinity and tensile strength. Microwave annealing method was also compared with conventional oven annealing method and results shows that microwave annealing significantly reduced the required annealing time to reach the maximum crystallinity and tensile strength. Notably, microwave annealing performed below cold crystallization temperature was exceptionally suitable to develop an optimized crystallinity and tensile strength for 3D printed PLA composite. Image 1 [ABSTRACT FROM AUTHOR]

Zeolitic imidazolate frameworks (ZIFs) can be used as an adsorbent to efficiently adsorb organic pollutants. However, ZIF nanoparticles are easy to form aggregates, hampering the effective and practical application in practical adsorption. In this study, the ZIF-8 was successfully loaded onto lignocellulose (LC) to further produce ZnO/LC by in situ growth method and hydrothermal treatment, and then Fe3O4 nanoparticles (Fe3O4 NPs) were loaded onto ZnO/LC to prepare magnetic Fe3O4/ZnO/LC adsorbent for removing tetracycline (TC) and congo red (CR) pollutants from aqueous solution. The adsorption properties of the adsorbent were systematically analyzed for different conditions, such as adsorbent dosage, solution pH, contact time, temperature and initial concentration. The experimental data were fitted using adsorption kinetic and isotherm models. The results showed that the pseudo-second-order model and Sips model were well fitted to the adsorption kinetic and adsorption isotherm, respectively. The adsorption capacities of TC and CR reached the maximum value of 383.4 mg/g and 409.1 mg/g in experimental conditions. The mechanism of the removal mainly includes electrostatic interaction, hydrogen bonding and π-π stacking. This novel adsorbent could be rapidly separated from the aqueous solution, suggesting its high potential to remove pollutants in wastewater. [ABSTRACT FROM AUTHOR]

Plant essential oils are widely used in food, medicine, cosmetics, and other fields because of their bacteriostatic properties and natural sources. However, the bacteriostatic range of unilateral essential oils is limited, and compound essential oil has become an effective way to improve the antibacterial properties of unilateral essential oils. In this study, based on the analysis of the antibacterial properties of Chinese cinnamon bark oil and oregano oil, the proportion and concentration of the compound essential oil were optimized and designed, and the antibacterial activity of the compound essential oil was studied. The results showed that the antibacterial activity of Chinese cinnamon bark oil was higher than that of oregano oil. The compound essential oil prepared by a 1:1 ratio of Chinese cinnamon bark oil and oregano oil with a concentration of 156.25 ppm showed an excellent antibacterial activity against Escherichia coli and Staphylococcus aureus. The GC-MS results showed that cinnamaldehyde was the main antibacterial component of Chinese cinnamon bark essential oil, and carvacrol and thymol in oregano oil were the main antibacterial components. [ABSTRACT FROM AUTHOR]

Since natural cellulose is mostly cellulose I and has a fibrous form, most cellulose-based adsorbents are fibrous/rod-shaped and exhibit the cellulose I crystal structure. This study reports a cellulose II-based spherical nanoparticle microcluster adsorbent (SNMA), synthesized from biomass by a bottom-up approach, for removing toxic hexavalent chromium (Cr(VI)). The basic structure of SNMA was investigated. Notably, the prepared adsorbent was a microcluster composed of spherical nanoparticles, while exhibiting cellulose II crystal structure, resulting in higher thermal stability and significantly enhanced adsorption performance. The adsorption process and mechanism of SNMA on Cr(VI) were studied in detail. The SNMA achieved a high adsorption capacity (225.94 mg/g) and receptor site density. The SNMA is expected to be used as a bio-based spherical nanoparticle microcluster adsorbent platform for the adsorption of different toxic substances by changing the surface functional groups of its components, spherical nanoparticles. [Display omitted] • The prepared adsorbent from biomass has a spherical nanoparticle microcluster morphology. • The obtained adsorbent exhibits cellulose II crystal structure. • The obtained adsorbent has good adsorption performance for Cr(VI). • It offered a strategy in preparing bio-based spherical nanoparticle microcluster adsorbent platform. [ABSTRACT FROM AUTHOR]

With the increase of sustainable development goal, the bio-based adsorption materials with high and selective dye removal are important for water treatment in the dyeing industry. In this paper, a bio-based adsorption foam composed of metal-organic frameworks (MOF) and polyethyleneimine (PEI)-modified cellulose was prepared by a three-step process, i.e., PEI modification of cellulose fibers (PC), MOF decoration of PEI-modified cellulose (MIL-53@PC), and in-situ foaming with polyurethane. PEI modification provides cellulose fiber with more active sites for both dye adsorption and MOF bonding. We found that MIL-53 crystals were tightly bonded on the surface of PC through hydrogen bonding. Because of the abundant adsorption sites (e.g., amines, iron oxide group), the MIL-53@PC demonstrated high adsorption capacity and selectivity for anionic dye (e.g., 936.5 mg/g for methyl orange) through electrostatic interaction and hydrogen bonding. Finally, MIL-53@PC particles were blended with a waterborne polyurethane prepolymer to prepare a three-dimensional hydrophilic foam (MIL-53@PC/PUF), which not only maintained high adsorption capacity and selectivity of MIL-53@PC and also improved its recyclability and reusability. The MIL-53@PC/PUF offers a promising solution for dye wastewater treatment. [Display omitted] • MIL-53@PC was fabricated via the ultrasonic method. • The maximum adsorption capacity of MIL-53@PC for MO was 936.5 mg/g. • The MIL-53@PC could selectively remove the anionic dyes from wastewater. • The MIL-53@PC/PUF broadened the practical application of powder adsorbent. [ABSTRACT FROM AUTHOR]

Polyvinyl alcohol (PVA) has been widely applied in industries for its low cost, nontoxicity, biodegradability, and renewable advantages. However, its unstable structure may not meet some strong physical and mechanical needs. In order to enhance the performances of the PVA film, cellulose nanocrystals (CNCs), tannic acid (TA), and chitosan (CS), working as a reinforcer, a crosslinker, and an antimicrobial agent, respectively, were introduced into the PVA matrix. The results indicated that CNCs, TA, and CS were evenly distributed and cohesively incorporated within the PVA matrix, which contributed to the good mechanical properties and thermal stabilities of biocomposite PVA films. Besides, the addition of TA remarkably improved the antiultraviolet and antioxidant capabilities of PVA films, although the light transmittance declined slightly. It was also observed that the pure PVA film and PVA reinforced with CNCs were incapable of protecting against bacteria, while the ones with CS had prominent antibacterial properties to Escherichia coli and Staphylococcus aureus. Overall, the resulting film presented a high potential utilization as a food packaging material for its outstanding physical and mechanical performances. [ABSTRACT FROM AUTHOR]

Background and Objectives. The development of network medicine provides new opportunities for disease research. Ischemic stroke has a high incidence, disability, and recurrence rate, and one of the reasons is that it is often accompanied by other complex diseases, including risk factors, complications, and comorbidities. Network medicine was used to try to analyze the characteristics of IS-related diseases and find out the differences in genetic pathways between Chinese herbs and Western drugs. Methods. Individualized treatment of traditional Chinese medicine (TCM) provides a theoretical basis for the study of the personalized classification of complex diseases. Utilizing the TCM clinical electronic medical records (EMRs) of 7170 in patients with IS, a patient similarity network (PSN) with shared symptoms was constructed. Next, patient subgroups were identified using community detection methods and enrichment analyses were performed. Finally, genetic data of symptoms, herbs, and drugs were used for pathway and GO analysis to explore the characteristics of pathways of subgroups and to compare the similarities and differences in genetic pathways of herbs and drugs from the perspective of molecular pathways of symptoms. Results. We identified 34 patient modules from the PSN, of which 7 modules include 98.48% of the whole cases. The 7 patient subgroups have their own characteristics of risk factors, complications, and comorbidities and the underlying genetic pathways of symptoms, drugs, and herbs. Each subgroup has the largest number of herb pathways. For specific symptom pathways, the number of herb pathways is more than that of drugs. Conclusion. The research of disease classification based on community detection of symptom-shared patient networks is practical; the common molecular pathway of symptoms and herbs reflects the rationality of TCM herbs on symptoms and the wide range of therapeutic targets. [ABSTRACT FROM AUTHOR]

In this work, tea powder was used as a filler to produce low-formaldehyde-emission tea-based melamine-modified urea–formaldehyde resin (TMUF). The thermal stabilities of TMUF and the resin without tea powder (MUF0) were characterized using thermogravimetry. The optimal amount of tea powder m(tea)/m(tea + urea) was equal to 0.15. The formaldehyde emission of the three-layer plywood produced by TMUF was reduced by 75.43%, and the wet bonding strength of the plate was increased by 26.67% as compared with the plywood prepared by MUF0. Compared with MUF0, the thermal degradation peak temperature of TMUF resin was shifted to higher temperature, while the carbon residue was increased. The thermal degradation activation energies of TMUF and MUF0 were similar, while TMUF had a lower pre-exponential A. The Flynn–Wall–Ozawa model-free method is used to estimate various activation energy values at different conversion rates and to predict possible reaction mechanisms. Judging the reaction mechanism according to the slope of the straight line fitted by different models, the best model was based on random nucleation. [ABSTRACT FROM AUTHOR]

Herein, a novel magnetic adsorbent (BC/AA/MN@Fe 3 O 4) was successfully prepared from waste bamboo fiber tissue and montmorillonite, and subsequently applied for the highly selective removal of malachite green (MG, removal efficiency = 97.3 %) from the mixed dye solution of MG with methyl orange (MO, removal efficiency = 4.5 %). The magnetic adsorbent has a high porosity with abundant mesopores. In the single dye MG solution, the adsorbent could effectively remove MG over a wide pH range from 4 to 10, and the maximum adsorption capacity (q max) was 2282.3 mg/g. Moreover, the magnetic adsorbent could remove MG from various solutions including mixed dye solution, high salinity solution, and real river water dye solution. The thermodynamic results proved that the adsorption process of MG was spontaneous and endothermic. The adsorption of MG was due to the comprehensive effects of electrostatic attraction, hydrogen bonding interactions and ions exchange, between the adsorbent and MG. Furthermore, the BC/AA/MN@Fe 3 O 4 exhibited an excellent reusability with adsorption efficiency above 53.4 % after five consecutive cycles. Therefore, the prepared magnetic nanocellulose-based adsorbent was expected to be a promising material for highly selective adsorption and separation of MG from mixed dye solution. • A novel magnetic adsorbent (BC/AA/MN@Fe 3 O 4) was successfully prepared. • It showed prominent uptake capability toward MG over a wide pH range from 4 to 10. • The calculated maximum adsorption capacity of BC/AA/MN@Fe 3 O 4 for MG was 2282.3 mg/g. • It can be effectively reused to selectively adsorb and separate MG from wastewater. [ABSTRACT FROM AUTHOR]

Herein, a novel magnetic adsorbent (BC/AA/MN@Fe 3 O 4) was successfully prepared from waste bamboo fiber tissue and montmorillonite, and subsequently applied for the highly selective removal of malachite green (MG, removal efficiency = 97.3 %) from the mixed dye solution of MG with methyl orange (MO, removal efficiency = 4.5 %). The magnetic adsorbent has a high porosity with abundant mesopores. In the single dye MG solution, the adsorbent could effectively remove MG over a wide pH range from 4 to 10, and the maximum adsorption capacity (q max) was 2282.3 mg/g. Moreover, the magnetic adsorbent could remove MG from various solutions including mixed dye solution, high salinity solution, and real river water dye solution. The thermodynamic results proved that the adsorption process of MG was spontaneous and endothermic. The adsorption of MG was due to the comprehensive effects of electrostatic attraction, hydrogen bonding interactions and ions exchange, between the adsorbent and MG. Furthermore, the BC/AA/MN@Fe 3 O 4 exhibited an excellent reusability with adsorption efficiency above 53.4 % after five consecutive cycles. Therefore, the prepared magnetic nanocellulose-based adsorbent was expected to be a promising material for highly selective adsorption and separation of MG from mixed dye solution. • A novel magnetic adsorbent (BC/AA/MN@Fe 3 O 4) was successfully prepared. • It showed prominent uptake capability toward MG over a wide pH range from 4 to 10. • The calculated maximum adsorption capacity of BC/AA/MN@Fe 3 O 4 for MG was 2282.3 mg/g. • It can be effectively reused to selectively adsorb and separate MG from wastewater. [ABSTRACT FROM AUTHOR]

In this study, the prepolymers (TYF) were prepared by formaldehyde and l -tyrosine, different amounts of TYF were added to prepare TYF modified urea-formaldehyde adhesives (LUF), and the gel time of resin, formaldehyde emission and wet shear strength of the plywood were tested. This result indicated that the optimal addition amount was 3 wt%, and the formaldehyde emission of plywood decreased by 23% to 0.57 mg/L, and the wet shear strength increased by 47% to 1.47 MPa. The thermal degradation and curing characteristics of urea-formaldehyde (UF) and LUF resins were characterized by thermogravimetric (TG) and differential scanning calorimetry (DSC), and the kinetic parameters were analyzed. The results showed that TYF could reduce the formaldehyde emission and improve the wet shear strength significantly. Moreover, the thermal degradation activation energy (E α) of UF resin was increased, and the thermal stability was enhanced. Although the initial and peak curing temperatures of LUF were higher, but the LUF cured more easily than the UF once the curing temperature was reached. [Display omitted] [ABSTRACT FROM AUTHOR]

Metal-organic frames (MOFs) have been recognized as one of the best candidates in the remediation of aqueous contaminants, while the fragile powder shape restricts the practical implementation. In this work, a shapeable, rebuildable, and multifunctional MOF composite (MIL-53@CF) was prepared from MIL-53 (Fe) and cellulose fiber (CF) using a simple ultrasonic method for adsorption and photocatalytic degradation of organic pollutants in wastewater. The results showed MIL-53(Fe) crystals were uniformly growth on CF surfaces and bonded with surface nanofibrils of CF through physical crosslinking and hydrogen bonding. Because of the high bonding strength, the MIL-53@CF composite exhibited an excellent compressive strength (3.53 MPa). More importantly, the MIL-53@CF composite was rebuildable through mechanical destruction followed by re-ultrasonication, suggesting the excellent reusability of MIL-53@CF for water remediation. The MIL-53@CF composite also had high adsorption capacities for methyl orange (884.6 mg·g−1), methylene blue (198.3 mg·g−1), and tetracycline (106.4 mg·g−1). MIL-53@CF composite could degrade TC through photocatalysis. The photocatalytic degradation mechanism was attributed to the Fe(II)/Fe(III) transform cycle reaction of MIL-53 crystal located on MIL-53@CF. Furthermore, the mechanical property and remoldability of MIL-53@CF composite increased its practicability. Comprehensively, MIL-53@CF composite provided a possible strategy to practically apply MOF in the remediation of aqueous contaminants. [Display omitted] • Shapeable, rebuildable, and multifunctional MIL-53@CF composite was synthesized using a simple ultrasonication method. • The MIL-53@CF is effective for adsorption and photocatalytic degradation of organic pollutants. • The mechanical properties, remoldability and recyclability of MIL-53@CF improved the practical application. • The synthesis, adsorption and catalytic mechanisms of MIL-53@CF composite were studied. [ABSTRACT FROM AUTHOR]

Applications of eco-friendly soy protein (SP) adhesives in the wood industry are restricted by their poor wet bonding strength and mold resistance. In this study, we noted that epoxy crosslinking agents not only have cross-linking properties, but also antifungal properties and can be used as cross-linkable antifungal agents to simultaneously improve the mold resistance and strength of SP adhesives. In order to develop sustainable and highly active epoxy cross-linkable antifungal agents, biomass-derived oxalic acid (OA) was converted into epoxy oxalic acid (EOA) with two electron-withdrawing ester groups, with 99.93% antifungal activity. The 1% ultra-low amount of EOA (when used as crosslinking agent) was uniformly dispersed in the uncured adhesive, prompting the anti-mold life of the adhesive to increase from 2 to 26 days. After curing, the tighter and more stable cross-linked network structure of the adhesive was constructed by the reaction of low reactive groups such as amide II bonds with ultra-low amounts of EOA, and the dry and wet shear strengths were increased by 49.0% and 139.7%, respectively, compared with pure adhesives. In addition, the anti-mold life of the cured adhesive increased from 4 to more than 30 days under the action of residual EOA. This work demonstrates the novel antifungal effect of epoxy crosslinkers, providing a controllable, green, and sustainable idea for the high-efficient improvement of mold resistance and strength of bio-based adhesives. • Epoxy crosslinkers generally have antifungal properties and can act as antifungal agents. • Epoxy oxalic acid (EOA) exhibited 99.93% antifungal activity, derived from inexpensive bio-based oxalic acid. • Soy protein functional groups cross-linked with EOA to construct a stable cross-linked network structure of the adhesive. • The bonding strength and mold resistance of the adhesive were efficiently enhanced by ultra-low levels of EOA. [ABSTRACT FROM AUTHOR]

Soy-based adhesives are considered to be a substitute for toxic petroleum-based adhesives in wood industry because of its environmentally-friendly property. However, their application range is limited by the lack of high wet bond strength and high toughness. While it is possible to impart these properties to soy-based adhesives by adding a variety of corresponding modifiers, it is difficult to do so by adding a single modifier. In this work, a multifunctional cross-linking agent dodecanedioic acid diglycidyl ester (DADE) with high reactivity, toughening, and hydrophobic effects was synthesized and incorporated into soy-based adhesive to ameliorate the bonding performance of the adhesives. The reaction process between DADE and protein was confirmed by instrumental analyses. Results revealed that the introduction of 4% DADE increased the wet bond strength of the soy protein adhesive by 140% to 1.57 MPa, whereas the wet bond strength (1.11 MPa) of soybean meal adhesive containing 4% DADE was comparable to that of MUF resin. The micrographs of the fracture surface and the force-distance curves of the shear strength test showed that the toughness of the adhesives was significantly improved by DADE. These improvements were attributed to the long hydrophobic aliphatic chains and highly reactive groups from DADE. This modification method avoided using large amounts of chemical additives. This work may provide an efficient and low-consumption method for producing bio-based adhesives with excellent bonding properties. [Display omitted] • The resulting soy-based adhesive was an environmentally-friendly wood adhesive. • A multifunctional crosslinker with toughening and hydrophobic effects was developed. • The use of DADE avoided the addition of additional hydrophobic and toughening agents. • The strength of the SPD adhesive was higher than that of formaldehyde-based resin. [ABSTRACT FROM AUTHOR]

Supramolecular structure of cellulosic materials from microwave treatment were throughly investigated for production of lignin-containing nanocellulose. The results revealed that both the intermolecular and intramolecular hydrogen bonds were altered by microwave irradiation. Cellulose I β was the main component in microwave treated bamboo (MTB) with smaller interplanar spacing, and the cellulose molecules were loosely connected resulting in a loose structure. Thereafter, MTB was used to produce lignin-containing nanocellulose by using oxalic acid dihydrate (OAD) to test the feasibility on its efficiency. The chemical consumed for the preparation of lignin-containing nanocellulose (LCN) with a comparable yield (68.08–82.33 %) from MTB was merely 1/10 that from conventional cellulosic materials, indicating the supramolecular structural changes of bamboo cellulose induced by microwave treatment provided suitable conditions for the subsequent hydrolysis of OAD to prepare LCN. The LCN was further added into the polyvinyl alcohol (PVA) matrix endowed excellent UV shielding property and thermal stability for the PVA/LCN films. This study was aimed to provide an environmentally friendly method on the production and application of LCN from bamboo by employing microwave treatment from the perspective of supramolecular level. [Display omitted] • Both the intermolecular and intramolecular hydrogen bonds were altered. • Cellulose molecules were loosely connected with smaller interplanar spacing. • LCN was produced from MTB with lower chemical consumption. [ABSTRACT FROM AUTHOR]

Sand blasting was proposed as a surface modification approach on the small diameter and thin culm wall bamboo species of Neosinocalamus affinis for the fabrication of laminated bamboo composites. The results revealed that sand blasting modification could almost wipe off the wax and silicons deposited on the green and yellow surfaces by removing or damaging the suberized and siliceous cells, pith membrane, and compact arranged sclereid, resulting in the uncovering of the porous structure. Meanwhile, the surface roughness was also increased by the sand blasting modification, which provided appropriate surface characteristics for resin permeability. The weight loss after sand blasting modification was merely 4.3%, and the internal structure was mostly preserved. Average modulus of rupture, modulus of elasticity, and compressive strength of the laminated bamboo composites fabricated from Neosinocalamus affinis were comparable to previous reported similar products and were higher than those from Phyllostachys pubescens and Phyllostachys bissetii. The findings in this study revealed that sand blasting modification could be used as an efficient and environmentally friendly approach on the high yield production of laminated bamboo composites from small diameter and thin culm wall bamboo species. • Sand blasting was efficient in cleaning up non-lignocellulosic substances on bamboo surfaces. • Laminated bamboo composites with yield of 96% was successfully fabricated. • The composites showed comparable mechanical strength with previously reported products. • Sand blasting surface modification was suitable for small diameter bamboo utilization. [ABSTRACT FROM AUTHOR]

Soy protein-based adhesives are biodegradable and renewable and are widely used in wood based products. However, the application of soy protein (SP) adhesives is also limited by its poor mildew resistance, water resistance and bonding strength, so it is necessary to find ways to promote the comprehensive performance of SP adhesives. In this study, hydroxymethyl l -tyrosine (TYF) synthesized from l -tyrosine and formaldehyde was used to enhance the mildew resistance and bonding strength of the SP adhesive. The results showed that the cross-linking reactions of TYF and SP molecules and the condensation reactions between an appropriate amount of TYF molecules enhanced the force between SP molecules and made the cross-linked structure more stable and compact, resulting in a significant increase in the bonding strength of the SP adhesive modified by TYF. Compared with the plywood prepared by the SPI adhesive, the SP adhesive modified with 6 wt% TYF had the best bonding performance, and its dry and wet shear strength were increased by 49.3% and 110.1%, respectively. In addition, l -tyrosine Schiff base, which had antibacterial, bactericidal and antiviral effects, was produced by dehydration of TYF molecules, so the mildew resistance of SP adhesives modified by TYF was effectively enhanced. [ABSTRACT FROM AUTHOR]

Although soy protein (SP) adhesives have shown great potential in promoting the green and sustainable development of the wood industry, the practical application of SP adhesives is limited by poor performance (bonging strength, mold resistance and water resistance). Cross-linking modification is considered to be the most effective modification method for SP adhesives. In this work, non-antibacterial l -tyrosine (TYR) was treated with epichlorohydrin to graft multiple epoxy groups and transformed into tetraepoxy l -tyrosine (ETY). Interestingly, ETY exhibited obvious antifungal properties with a bacteriostatic rate as high as 98.3%. Adding a low amount (3 wt%) of ETY, the wet shear strength of the modified adhesive was 169.1% higher than that of the pristine SP adhesive, reaching 1.83 MPa. Moreover, in an environment of 28 °C and 80% humidity, both uncured and cured SP adhesives (with 3 wt% ETY) exhibited an anti-mold period of more than 30 days. Therefore, this work reveals that non-antibacterial bio-based materials may be endowed with antibacterial properties through epoxidation and transformed into multifunctional modifiers, and provides a new way for the development of high-strength antibacterial bio-based adhesives. • Non-antibacterial bio-based materials may be endowed with antibacterial properties through epoxidation. • The antibacterial rate of tetraepoxy l -tyrosine is as high as 98.3%. • High performance adhesive modified by low amount of ETY. • The wet shear strength of the adhesive (with 3 wt% ETY) increased by 169.1% to 1.83 MPa. • Modified adhesives (with 3 wt% ETY) showed an anti-mold period of more than 30 days. [ABSTRACT FROM AUTHOR]

[Display omitted] • The fracture toughness of bamboo increased with the water content. • One function of water in bamboo was to soften the cell wall, which increased the plastic deformation of bamboo and impeded the propagation of cracks. • The other function of water in bamboo was to make the fracture surface smooth, which indicates that cracks propagated easily. • These two functions of water also affected the fracture toughness of other materials. Most engineering materials are chosen based on their fracture toughness rather than their strength. However, water molecules in air would interact with these materials and affect their fracture toughness, especially for the biomass materials. Bamboo is an excellent engineering material, and the effect of water content on its fracture toughness was still unknown. Thus, in this study, the effect of water on bamboo's fracture toughness was investigated, and the mechanism behind it was discussed. The results showed that the growth fracture toughness increased by 7.6 J/m2 per 1 % increase of environmental relative humidity. The effect of the water includes both promoting and impeding crack growth. The hydrated amorphous layer in cell wall impeded the propagation of cracks, while the water layer on cell wall promoted the propagation of cracks. The former effect was the stronger one in bamboo, and thus the fracture toughness increased. This competition mechanism stemmed from water was also found useful to explain the fracture properties of other kinds of materials, such as wood, stone, and clay. Therefore, a reasonable hypothesis to explain the mechanism of water content on fracture toughness of bamboo and even other materials was concluded in this study. [ABSTRACT FROM AUTHOR]

This work prepared a double-cross-linked biohybrid aerogel (DCBA) bead biosorbent from waste bamboo paper and chitosan by sequential physical (hydrogen bonding and electrostatic interaction between -COO- and -NH 3 + groups) and chemical (polymerization reaction between -COOH and -NH 2 , dehydration condensation between Si-OH and -OH) cross-linkings. The resulting DCBA bead was applied to remove cationic (Methylene blue, MB) and anionic (Congo red, CR) dyes in both single and binary systems. The MB and CR adsorption capacities of DCBA bead increased with increasing adsorbent dosage, contact time, temperature and initial dye concentration. With increasing solution pH, the MB adsorption capacity increased, while that for CR increased first and then decreased. The maximal adsorption capacities for MB and CR were 653.3 and 559.6 mg/g, respectively, in the single system. The thermodynamic analysis results showed a spontaneous and endothermic adsorption process. DCBA bead had a good stability and reusability with the removal efficiencies of 49.4% and 60.6% for MB and CR, respectively, after five cycles of adsorption-desorption. In the binary system, the adsorption of MB was inhibited by CR, while the removal of CR was enhanced by MB. • DCBA biosorbent was prepared using double cross-linking method. • The DCBA bead exhibited excellent stability and recyclability. • The maximum adsorption capacities of MB was 653.3 mg/g. • The maximum adsorption capacities of CR was 559.6 mg/g. • The adsorption mechanisms in single and binary systems were investigated. [ABSTRACT FROM AUTHOR]

In this work, ethyl acetate (EA) and trichloromethane (TR) extracts were extracted from Phoebezhennan wood residues and the extracts were then applied to the preparation of UV shielding films (UV-SF). The results revealed that substances including olefins, phenols and alcohols were found in both EA and TR extracts, accounting for about 45% of all the detected substances. The two extracts had similar thermal stability and both had strong UV shielding ability. When the relative percentage of the extract is 1 wt% in solution, the extract solution almost blocked 100% of the UV-B (280–315 nm), and UV-A (315–400 nm). Two kinds of UV-SF were successfully prepared by adding the two extracts into polylactic acid (PLA) matrix. The UV-SF with the addition of 24 wt% of the extractive blocked 100% of the UV-B (280–315 nm) and more than 80% of the UV-A (315–400 nm). Moreover, the UV shielding performance of the UV-SF was still stable even after strong UV irradiation. Though the addition of extracts could somewhat decrease the thermal stability of the film, its effect on the end-use of the film was ignorable. EA extracts had less effect on the tensile properties of the films than TR extracts as the content of the extract reached 18%. The results of this study could provide fundamental information on the potential utilization of the extracts from Phoebe zhennan wood residues on the preparation of biobased UV shielding materials. [ABSTRACT FROM AUTHOR]