Publications by authors named "Xuedong Xi"

Starch adhesives have gained popularity due to their unique properties, which include a range of raw materials, simplicity of separation and purification, high yield, non-toxicity, and biodegradability. However, starch-based adhesives have weaknesses such as poor bonding effectiveness, poor water resistance, and poor mildew resistance. This study aims to solve these shortcomings and make such adhesives useful in the wood processing industry.

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Conventional wood adhesives such as urea-formaldehyde (UF) resin, phenol-formaldehyde (PF) resin, melamine-formaldehyde (MF) resin, and melamine-urea-formaldehyde (MUF) resin have usually problems in formaldehyde emission and derived from petrochemical products, so developing green and environmentally friendly biomass-based wood adhesives has become a research topic of wide focus. As a biomaterial, cellulose (and its derivatives) is the largest bio-resource in the world, and developing its application in wood adhesives synthesis has outstanding raw material advantage. Therefore, in this study, a formaldehyde-free cellulose-based wood adhesive (OCHU) was prepared from carboxymethyl cellulose (CMC) by oxidizing with NaIO and then cross-linked with a laboratory synthetic polyurea compound (HU).

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Article Synopsis
  • * Key factors affecting adsorption performance included the mass ratio of tannin to chitosan, pH levels, adsorption time, and initial metal ion concentrations, with a maximum adsorption capacity of 37.6 mg/g for Cu and 52.9 mg/g for Pb.
  • * The adsorption process primarily involved single-layer chemical adsorption and demonstrated high removal efficiencies of 82% for Cu and 95% for Pb, with the ability to release the adsorbed ions using a dilute strong acid.
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  • Biomass-based non-isocyanate polyurethane (NIPU) is gaining attention in the polyurethane industry for its sustainable materials and lack of toxic isocyanates.
  • This study focuses on lignin, a renewable natural polymer, to create lignin-based NIPU (L-NIPU) foams using maleic acid as an initiator and glutaraldehyde as a cross-linker, producing lightweight and strong materials.
  • The optimal composition of 18% maleic acid and 25% glutaraldehyde yields foams with significant compressive strength (up to 0.5 MPa) and low thermal conductivity (0.03559 W/m·K), making them suitable for insulation in construction
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Article Synopsis
  • - The study focuses on creating a new wood adhesive called OCHU, made from oxidized cellulose combined with hexamethylene diamine and urea, which shows high bonding strength and excellent water resistance.
  • - To enhance the cellulose, it undergoes enzymatic hydrolysis and oxidation, increasing its solubility and the number of reactive groups, leading to better adhesive properties.
  • - The OCHU adhesive proves its effectiveness with significantly improved wet strength—60% stronger than its predecessor (OCH)—and shows potential for widespread use in the plywood industry due to its superior performance.
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The preparation and application of non-isocyanate polyurethane (NIPU) from biomass raw materials as a substitute for traditional polyurethane (PU) has recently become a research hot topic as it avoids the toxicity and moisture sensitivity of isocyanate-based PU. In the work presented here, self-blowing GNIPU non-isocyanate polyurethane (NIPU) rigid foams were prepared at room temperature, based on glucose, with acids as catalysts and glutaraldehyde as a cross-linker. The effects of different acids and glutaraldehyde addition on foam morphology and properties were investigated.

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Article Synopsis
  • * The improved adhesive system significantly increased the bonding strength of plywood and particleboard, showing percentage increases of 15-17% when dry and up to 82% after boiling for particleboard, and 37% to 90% for plywood at various tests.
  • * Key reasons for increased strength included a more controlled cross-linking process, higher pH shifting the polycondensation equilibrium, and enhanced interaction between the adhesive and wood at the molecular level.
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Starch adhesive is a commonly used bonding glue that is sustainable, formaldehyde-free and biodegradable. However, there are obviously some problems related to its high viscosity, poor water and mildew resistance. Hence, exploring a starch-based adhesive with good properties that satisfies the requirements of wood processing presents the context of the current research.

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Wood-based panels find widespread application in the furniture and construction industries. However, over 90 % of adhesives used are synthesized with formaldehyde, leading to formaldehyde emission and associated health risks. In this study, an entirely bio-based adhesive (OSL) was innovatively proposed through the condensation of multi-aldehyde derived from the oxidization of sucrose (OS) with sodium lignosulfonate (L).

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Non-isocyanate polyurethane (NIPU) as a new type of polyurethane material has become a hot research topic in the polyurethane industry due to its no utilization of toxic isocyanates during the synthesis process. And the developing on recyclable biomass materials has also much attention in the industrial sector, hence the preparation and application of bio-based NIPU has also become a very meaningful study work. So, in this paper, tannin as a biomass material was used to synthesize tannin based non-isocyanate polyurethanes (TNIPU) resin, and then successfully prepared a self-blowing TNIPU foam at room temperature by using formic acid as initiator and glutaraldehyde as cross-linking agent.

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Despite the widespread application prospect of soybean meal flour (SF) as a non-toxic and renewable wood adhesive, the practical application is limited by its poor mechanical properties and water resistance. In this work, a novel SF-based wood adhesive (CSP) was developed using citric acid (CA) as a modifier, which was further designated to produce plywood on a laboratory scale. Moreover, the effects of the mass ratio of CA/SF, hot-pressing temperature, and hot-pressing time on the bonding properties and water resistance of the resulting plywood were investigated in detail.

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Starch is one of the important raw materials for the preparation of biomass adhesives for its good viscosity and low-cost properties. However, the drawbacks of poor water resistance and bonding performance seriously restrict its application in the wood industry. To resolve those problems, an environment-friendly renewable, and high water resistance starch-based adhesive (OSTH) was prepared with oxidized starch and hexanediamine by Schiff base reaction.

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Starch adhesive, as a sustainable biomass-based adhesive, could be used to solve environmental problems from petroleum-derived adhesive. But its application is hindered by poor water resistance, mildew resistance, and storage stability. Here, a fully bio-based citric acid-starch adhesive (CASt) with high properties was successfully introduced by a simple method.

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Condensed tannin copolymerized with hyperbranched tris(2-aminoethyl)amine-urea formed by amine-amido deamination yields a particleboard thermosetting adhesive without any aldehydes satisfying the requirements of relevant standards for the particleboard internal bond strength. The tannin-triamine-urea cures well at 180 °C, a relatively low temperature for today's particleboard hot pressing. As aldehydes were not used, the formaldehyde emission was found to be zero, not even in traces due to the heating of wood.

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As a biomass material, tannins are used in the preparation of wood adhesives, but their poor strength and water resistance has greatly limited their application. Therefore, it is necessary to prepare tannin-based wood adhesives with good water resistance. In the present study, tannin and hexanediamine were simply mixed at room temperature to prepare tannin-hexanediamine (TH) adhesive and then used to prepare plywood.

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Glyoxal is considered to be the most likely substitute for formaldehyde to synthesize resin adhesives for wood bonding due to its reactivity, structural characteristics, being non-toxic, low volatility, and acceptable cost. Regrettably, the performance of the resin synthesized using glyoxal to directly replace all formaldehyde is not totally satisfactory, especially as it has almost no water resistance. This makes such a simple alternative fail to be suitable for industrial production.

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Biomass-based adhesives have attracted much attention due to their eco-friendly, sustainable characteristics compared to formaldehyde-based adhesives; however, their low bonding strength and water resistance restrict their application. Thus, developing a high-performance biomass-based adhesive with excellent bonding strength and water resistance is necessary. In this work, a fully biomass-based citric acid-glucose (CAG) adhesive was produced by the esterification reaction of glucose and citric acid, which was validated by Fourier transform infrared (FT-IR), C nuclear magnetic resonance (C NMR), and liquid chromatography-mass spectrometry (LC-MS).

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Synthetic foams have become an essential industrial product for a great variety of applications. Furfuryl alcohol, as a biomass chemical, was reacted with glyoxal at room temperature to prepare furanic-glyoxal rigid foams, and p-toluenesulfonic acid was used as a catalyst to initiate the reaction. Foams with different molar ratios (furfuryl alcohol/glyoxal) were prepared in this work, and uniform cells foams have been obtained.

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Ambient temperature self-blowing mimosa tannin-based non-isocyanate polyurethane (NIPU) rigid foam was produced, based on a formulation of tannin-based non-isocyanate polyurethane (NIPU) resin. A citric acid and glutaraldehyde mixture served as a blowing agent used to provide foaming energy and cross-link the tannin-derived products to synthesize the NIPU foams. Series of tannin-based NIPU foams containing a different amount of citric acid and glutaraldehyde were prepared.

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A partially biobased self-blowing and self-hardening polyurethane foam from glucose-based non-isocyanate polyurethanes (g-NIPU) was prepared by reaction of glucose with dimethyl carbonate and hexamethylene diamine. However, these foam types generally require a high foaming temperature. In this paper, a self-blowing foam based on g-NIPU was prepared at room temperature by using maleic acid as an initiator and glutaraldehyde as a crosslinker.

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Soy protein isolate (SPI) and insoluble soy flour polymeric carbohydrates have been reacted with sodium periodate for the specific oxidation of vicinal -OH groups to investigate the reactions involved in this approach to soy flour adhesives. The reactions have been shown to generate carbohydrate oligomer fractions presenting one, two or multiple aldehyde groups. With the exception of the small molecular weight heptanedial, the smaller molecular weight aldehydes generated from mono- and disaccharides by the same reaction do not appear to form from the insoluble soy flour carbohydrates, or have already reacted.

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Tannin and lignin were blended with polypropylene (PP) through dynamic vulcanization technique. Their influence of mechanical property, crystallinity, thermal stability, as well as ultraviolet (UV) protection property on the PP matrix was investigated and compared with native tannin and lignin. According to our experimental results, tannin and lignin undergo dynamic vulcanization and were more compatible with the PP matrix.

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Two novel depsipeptides xenematides F and G (1, 2), were isolated from entomopathogenic Xenorhabdus budapestensis SN84 along with a known compound xenematide B. The structures of the two new molecules were elucidated using NMR, MS and Marfey's method. The xenematide G (2) contains α-aminoheptanoic acid, a non-protein amino acid that is rarely found in secondary metabolites from entomopathogenic bacteria.

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Mostly biosourced non-isocyanate polyurethanes (NIPU) were prepared from mono- and disaccharides, namely glucose and sucrose, reacted with dimethyl carbonate and hexamethylene diamine. The main aim of this research was to show that NIPU can be prepared from mono- and disaccharides, this just being an initial exploratory work and its sole main aim. The oligomers obtained were detected by MALDI-ToF, CP-MAS C NMR, and FTIR spectrometries.

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The reaction of citric acid with wood veneers was studied by Cross Polarization Magic Angle Spinning Nuclear Magnetic Resonance (CP MAS C NMR) and matrix assisted laser desorption ionization time of flight (MALDI ToF) mass spectrometry. The analysis showed that reactions of citric acid occurred with both lignin and carbohydrate constituents of wood. The reactions occurring are esterifications between the carboxylic acid functions of citric acid and the numerous aromatic and aliphatic hydroxyl groups of the main wood constituents.

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