Epoxy resins are widely employed in wind turbine blades,drone rotors,and automotive interiors due to their excel-lent mechani-cal proper-ties and long service life.However,their insoluble and infusible cross-linked ne...Epoxy resins are widely employed in wind turbine blades,drone rotors,and automotive interiors due to their excel-lent mechani-cal proper-ties and long service life.However,their insoluble and infusible cross-linked networks pose a significant re-cycling challenge,particularly with the impending retirement of the first generation of wind turbine blades.In this work,we reported a fully bio-based epoxy Vitrimer(FEP)incorporat-ing a dual-dynamic covalent network design and systematically investigated the influence of the 1,5,7-triazabicyclo[4.4.0]dec-5-ene(TBD)catalyst on its curing kinetics,thermal/mechan-ical properties,dynamic exchange behavior,and degradation performance in a mild alkaline solution.Compared to conventional epoxy resins,FEP exhibited superior tensile strength and elongation at break at an optimal TBD concentration(2 wt%),achieving an excellent strength-toughness balance.The presence of TBD accelerated the exchange rates of both disulfide and ester bonds,endowing FEP with notable stress relaxation at elevated tempera-tures.Moreover,FEP demonstrated complete dissolution in 1 mol/L NaOH within 6 h at 25℃.These results underscored the exceptional strength,toughness,and recyclability of FEP,positioning it as a promising,environmentally friendly matrix resin for next-generation appli-cations in the new energy sector.展开更多
Developing green and efficient methods to acquire lignocellulose-based chemicals with high added value is beneficial for facilitating green chemistry and sustainable development.The goal of this study is to demonstrat...Developing green and efficient methods to acquire lignocellulose-based chemicals with high added value is beneficial for facilitating green chemistry and sustainable development.The goal of this study is to demonstrate that bio-based benzaldehyde,a noteworthy high-value chemical,is able to be directionally prepared from lignocellulosic biomass.This new control-lable transformation was materialized by uniting catalytic-pyrolysis of lignocellulose to toluene intermediate and catalytic oxidation of toluene intermediate to bio-based benzalde-hyde.This work also developed a highly active magnetic catalyst(CoFe_(2)O_(4)@Biochar(HTR)),achieving 77.1%benzaldehyde selectivity and 46.7%benzaldehyde yield using this catalyst.It was found that introducing the biochar carrier into the cobalt iron composite metal oxide cat-alyst enhanced hydroxyl radical formation and bio-based benzaldehyde synthesis.Based on catalyst characterizations and hydroxyl radical analysis,potential reaction mechanism for bio-based benzaldehyde synthesis was proposed.This strategy may provide a beneficial pathway for developing high-value bio-based chemical(benzaldehyde)using renewable lignocellulosic biomass.展开更多
This study aims to develop highly hygroscopic bio-based co-polyamides(CPs)by melt co-polycondensation of polyamide(PA)56 salt and PA66 salt with varying molar fractions.The functional groups and the chemical structure...This study aims to develop highly hygroscopic bio-based co-polyamides(CPs)by melt co-polycondensation of polyamide(PA)56 salt and PA66 salt with varying molar fractions.The functional groups and the chemical structure of the prepared samples were determined by Fourier transform infrared(FTIR)spectroscopy and proton nuclear magnetic resonance(^(1)H-NMR)spectroscopy.The relative viscosity was determined with an Ubbelohde viscometer.The melting behavior and the thermal stability of CPs were investigated by differential scanning calorimetry(DSC)and thermogravimetric analysis(TGA).Furthermore,the water absorption behavior of CP hot-pressed film was studied.The results reveal that the melting point,the crystallization temperature and the crystallinity of CPs firstly decrease and then increase with the molar fraction of PA66 in CPs.The copolymerization of PA56 with PA66 leads to an obvious increase in water absorption.The CPs with PA66 molar fraction of 50%possess a high saturated water absorption rate of 17.6%,compared to 11.6%for pure PA56 and 7.8%for pure PA66.展开更多
Novel bio-based and biodegradable block copolymers were synthesized by "click" reaction between poly(L-lactide)(PLLA) and polyamide 4(PA4). Upon tuning the molar mass of PLLA block, the properties of copolym...Novel bio-based and biodegradable block copolymers were synthesized by "click" reaction between poly(L-lactide)(PLLA) and polyamide 4(PA4). Upon tuning the molar mass of PLLA block, the properties of copolymers and electrospun ultrafine fibers were investigated and compared with those of PLLA and PA4 blends. PLLA and PA4 were found incompatible and formed individual crystalline regions, along with reciprocal inhibition in crystallization. Electrospun fibers were highly hydrophobic, even if hydrophilic PA4 was the rich component. The crystallinity of either PLLA or PA4 decreased after electrospinning and PLLA-rich as-spun fibers were almost amorphous. Immersion tests proved that fibers of block copolymers were relatively homogeneous with micro-phase separation between PLLA and PA4. The fibrous structures of copolymers were different from those of the fibers electrospun from blends, for which sheath-core structure induced by macro-phase separation between homopolymers of PLLA and PA4 was confirmed by TEM, EDS, and XPS.展开更多
The objective of this study was to improve the toughness of bio based brittle poly(ethylene 2,5-furandicarboxylate)(PEF)by melt blending with bio based polyamide11(PA11)in the presence of a reactive multifunctional ep...The objective of this study was to improve the toughness of bio based brittle poly(ethylene 2,5-furandicarboxylate)(PEF)by melt blending with bio based polyamide11(PA11)in the presence of a reactive multifunctional epoxy compatibilizer(Joncryl ADR-4368).The morphological,thermal,rheological,and mechanical properties of PEF/PA11 blends were investigated.Compared with neat PEF,the toughness of PEF/PA11 blend was not improved in the absence of the reactive compatibilizer due to the poor compatibility between the two polymers.When Joncryl was incorporated into PEF/PA11 blends,the interfacial tension between PEF and PA11 was obviously reduced,reflecting in the fine average particle size and narrow distribution of PA11 dispersed phase as observed by scanning electron microscopy(SEM).The complex viscosities of PEF/PA11 blends with Joncryl were much higher than that of PEF/PA11 blend,which could be ascribed to the formation of graft copolymers through the epoxy groups of Joncryl reacting with the end groups of PEF and PA11 molecular chains.Thus,the compatibility and interfacial adhesion between PEF and PA11 were greatly improved in the presence of Joncryl.The compatibilized PEF/PA11 blend with 1.5 phr Joncryl exhibited significantly improved elongation at break and unnotch impact strength with values of 90.1%and 30.3kJ/m2,respectively,compared with those of 3.6%and 3.8 kJ/m2 for neat PEF,respectively.This work provides an effective approach to improve the toughness of PEF which may expand its widespread application in packaging.展开更多
With the escalating global emphasis on environmental conservation and sustainable development,enhancing the service quality and durability of road surfaces and facilitating the green development of highways have comma...With the escalating global emphasis on environmental conservation and sustainable development,enhancing the service quality and durability of road surfaces and facilitating the green development of highways have commanded considerable attention.Bio-based polyurethane,on account of its remarkable physical and chemical properties,green,sustainable and renewable capacity,as well as its structural design capabilities,has drawn widespread attention and numerous studies have been carried out.It has gradually started to substitute traditional petroleum-based polyurethane materials in road engineering.Nevertheless,the application of bio-based polyurethane materials in road engineering remains in the exploratory phase.To stimulate the application research of bio-based polyurethane materials in road engineering and offer additional research directions,this paper reviews the research advancements of bio-based polyurethane materials and their applications in road engineering.The fundamental classification of bio-based polyurethane is introduced.The characteristics and challenges associated with various preparation methods for bio-based polyurethane are described.The influence of bio-based polyurethane on road engineering materials are analyzed.The evaluation indicators of bio-based polyurethane within the life cycle of road engineering are investigated.Finally,the development tendency towards in road engineering applications are forecasted.This paper provides a reference for the study of bio-based polyurethane materials in road engineering applications.展开更多
The current global shortage of oil resources and the pollution problems caused by traditional barrier materials urgently require the search for new substitutes.Biodegradable bio-based barrier materials possess the cha...The current global shortage of oil resources and the pollution problems caused by traditional barrier materials urgently require the search for new substitutes.Biodegradable bio-based barrier materials possess the characteristics of being renewable,environmentally friendly,and having excellent barrier properties.They have become an important choice in fields such as food packaging,agricultural film covering,and medical protection.This review systematically analyzes the design and research of this type of material,classifying biobased and biodegradable barrier materials based on the sources of raw materials and synthesis pathways.It also provides a detailed introduction to the latest research progress of biobased and biodegradable barrier materials,discussing the synthesis methods and improvement measures of their barrier properties.Subsequently,it analyzes the related technologies for enhancing the barrier properties of biobased and biodegradable barrier materials,and finally looks forward to the directions that future research should focus on,promoting the transition of biobased and biodegradable barrier materials from the laboratory to industrial applications.展开更多
The demand for energy-efficient and environmental-friendly power grid construction has made the exploitation of bio-based electrical epoxy resins with excellent properties increasingly important.This work developed th...The demand for energy-efficient and environmental-friendly power grid construction has made the exploitation of bio-based electrical epoxy resins with excellent properties increasingly important.This work developed the bio-based electrotechnical epoxy resins based on magnolol.High-performance epoxy resin(DGEMT)with a double crosslinked points and its composites(Al_(2)O_(3)/DGEMT)were obtained taking advantages of the two bifunctional groups(allyl and phenolic hydroxyl groups)of magnolol.Benefitting from the distinctive structure of DGEMT,the Al_(2)O_(3)/DGEMT composites exhibited the advantages of intrinsically high thermal conductivity,high insulation,and low dielectric loss.The AC breakdown strength and thermal conductivity of Al_(2)O_(3)/DGEMT composites were 35.5 kV/mm and 1.19 W·m-1·K-1,respectively,which were 15.6%and 52.6%higher than those of petroleum-based composites(Al_(2)O_(3)/DGEBA).And its dielectric loss tanδ=0.0046 was 20.7%lower than that of Al_(2)O_(3)/DGEBA.Furthermore,the mechanical,thermal and processing properties of Al_(2)O_(3)/DGEMT are fully comparable to those of Al_(2)O_(3)/DGEBA.This work confirms the feasibility of manufacturing environmentally friendly power equipment using bio-based epoxy resins,which has excellent engineering applications.展开更多
By investigating the performance characteristics of the bio-based surfactant 8901A,a composite decontamination and injection system was developed using 8901A as the primary agent,tailored for application in low-permea...By investigating the performance characteristics of the bio-based surfactant 8901A,a composite decontamination and injection system was developed using 8901A as the primary agent,tailored for application in low-permeability and heavy oil reservoirs under varying temperature conditions.The results demonstrate that this system effectively reduces oil–water interfacial tension,achieving an ultra-low interfacial tension state.The static oil washing efficiency of oil sands exceeds 85%,the average pressure reduction rate reaches 21.55%,and the oil recovery rate improves by 13.54%.These enhancements significantly increase the system’s ability to dissolve oilbased blockages,thereby lowering water injection pressure caused by organic fouling,increasing the injection volume of injection wells,and ultimately improving oil recovery efficiency.展开更多
Aging plays a critical role in determining the durability and long-term performance of asphalt pavements,as it is influenced by both external factors(e.g.,temperature,ultraviolet(UV)radiation,moisture,oxidative gases)...Aging plays a critical role in determining the durability and long-term performance of asphalt pavements,as it is influenced by both external factors(e.g.,temperature,ultraviolet(UV)radiation,moisture,oxidative gases)and internal factors such as binder composition.Although laboratory simulations of aging are well established for conventional bituminous binders,limited attention has been paid to replicating and evaluating aging processes in bio-based binders.This review provides a comprehensive analysis of current laboratory techniques for simulating and assessing binder aging,with a focus on two key areas:aging simulation protocols and evaluation methodologies.The analysis shows that although several efforts have been made to incorporate external aging factors into lab simulations,significant challenges persist,especially in the case of bio-based binders,which are characterized by a high variability in composition and limited understanding of their aging behavior.Current evaluation approaches also exhibit limitations.Improvements are needed in the molecular-level analysis of oxidation(e.g.,through more representative oxidation modelsin molecular dynamicssimulations),in the separation and quantification of binder constituents,and in the application of advanced techniques such as fluorescence microscopy to better characterize polymer dispersion.To enhance the reliability of laboratory simulations,future research should aim to improve the correlation between laboratory and field aging,define robust aging indexes,and refine characterization methods.These advancements are particularly critical for bio-based binders,whose performance is highly sensitive to aging and for which standard test protocols are still underdeveloped.A deeper understanding of aging mechanisms in both polymer-modified and biobased binders,along with improved analytical tools for assessing oxidative degradation and morphological changes,will be essential to support the development of sustainable,high-performance paving materials.展开更多
In the context of transitioning toward more sustainable construction materials,this study explores the impact of incorporating millet husks as an alternative to sand on the physical,mechanical,and thermal performance ...In the context of transitioning toward more sustainable construction materials,this study explores the impact of incorporating millet husks as an alternative to sand on the physical,mechanical,and thermal performance of lightweight concrete.Through a mixture design approach,five formulations were selected and thoroughly characterized.The analysis of iso-response curves enabled an in-depth assessment of the cross-effects between formulation parameters and their interactions on the final properties of the material.The results show that integrating millet husks leads to a significant reduction in density,reaching up to 21%,while maintaining notable mechanical performance.A balanced formulation of sand and fibers achieved a maximum compressive strength of 12.11 MPa,demonstrating that,under specific conditions,plant fibers actively contribute to the structural integrity of the composite.In tensile strength,the positive influence of fibers is even more pronounced,with a maximum resistance of 8.62 MPa,highlighting their role in enhancing material cohesion.From a thermal perspective,millet husks reduce both thermal conductivity and effusivity,thereby limiting heat transfer and accumulation within the composite.Iso-response curve analysis reveals that these effects are directly linked to the proportions of the constituents and that achieving an optimal balance between sand,fibers,and cement is key to maximizing performance.These findings demonstrate that the adopted approach allows moving beyond conventional substitution methods by identifying optimal configurations for the design of lightweight bio-based concretes that are both strong and insulating,thereby confirming the potential of millet husks in developing lightweight concretes suitable for sustainable construction applications.展开更多
An efficient and novel approach is proposed for oxidative arylation of bio-based furfuryl alcohol(FA)to aryl furans(AFs),a versatile monomer of photoelectric materials,in the presence of UiO-67-Pd(F)with phenanthrolin...An efficient and novel approach is proposed for oxidative arylation of bio-based furfuryl alcohol(FA)to aryl furans(AFs),a versatile monomer of photoelectric materials,in the presence of UiO-67-Pd(F)with phenanthroline/bipyridine,and poly-F substituted phenyl ligands as the mixture linkers.The results of control experiments and theoretical calculations reveal that the–F on the phenyl linkers efficiently tunes the electron-deficient nature of Pd through the Zr_(6) clusters bridges,which favors the adsorption and activation of the furan ring.Furthermore,the conjugation of different nitrogen-containing ligands facilitates Pd coordination for the Heck-type insertion and subsequent electrophilic palladation,respectively.As a result,the oxidative arylation of FA derivatives is substantially enhanced because of these electronic and steric synergistic effects.Under the optimized conditions,72.2%FA conversion and 74.8%mono aryl furan(MAF)selectivity are shown in the Heck-type insertion.Meanwhile,85.3%of MAF is converted,affording 74.8%selectivity of final product(AFs)in the subsequent electrophilic palladation reaction.This process efficiency is remarkably higher than that with homogeneous catalysts.In addition,furan-benzene polymer obtained from the halogen-free synthesis catalyzed by UiO-67-Pd(F)show significantly better properties than that from conventional Suzuki coupling method.Therefore,the present work provides a new insight for useful AFs synthesis by oxidative arylation of bio-furan via rational tunning the metal center micro-environment of heterogeneous catalyst.展开更多
Nanofiltration(NF) technology,with its capacity for nanoscale filtration and controllable selectivity,holds significant promise in diverse applications.However,the current upper bound of permeance and selectivity of N...Nanofiltration(NF) technology,with its capacity for nanoscale filtration and controllable selectivity,holds significant promise in diverse applications.However,the current upper bound of permeance and selectivity of NF membranes is intrinsically constrained by the morphology and structure of the polyamide(PA) selective layer.This issue arises because NF membranes typically exhibit relatively smooth nodular structures,which theoretically impede efficient water transport.In this study,we enhanced the formation of nanobubbles by synergistically regulating with surfactant and low temperatures,resulting in the fabrication of PA NF membranes with a crumpled morphology.We observed that lower temperatures promote enhanced gas solubility in the aqueous phase,facilitating increased nanobubble formation through the foaming effect of surfactant sodium dodecylbenzene sulfonate(SDBS).Consequently,this resulted in the creation of PA NF membranes with more crumpled structures and superior performance,with pure water permeance reaching 36.25 ± 0.42 L m^(-2)h^(-1)bar^(-1),representing an improvement of 14.47 L m^(-2)h^(-1)bar^(-1)compared to the control group.Additionally,it maintains a high Na_(2)SO_(4) rejection rate of97.00 % ± 0.58 %.The PA NF membranes produced by eliminating nanobubbles and free interfaces exhibited a smooth structure,whereas introducing nanobubbles(through Na HCO_(3) addition,N_(2) pressurization,and ultrasonication) resulted in the formation of crumpled membranes.This emphasized that the large amount of nanobubbles generated by SDBS and low temperature in the interfacial process played a critical role in shaping crumpled PA NF membranes and enhancing membrane performance.This approach has the potential to provide valuable insights into customizing the structural design of TFC PA NF membranes,contributing to further advancements in this field.展开更多
The chemical structure of polyamide 6(PA6)dictates that only 50%of hydrogen bonds participate in crystallization during the crystallization process,resulting in the properties of its products being significantly depen...The chemical structure of polyamide 6(PA6)dictates that only 50%of hydrogen bonds participate in crystallization during the crystallization process,resulting in the properties of its products being significantly dependent on the molding process.Therefore,the design and development of nucleating agents suitable for PA6 holds great practical significance for high-performance PA6 materials.Amide-based nucleating agents can effectively improve the crystallization rate by increasing intermolecular hydrogen bond density.Further introduction of hydroxyl groups can enhance the hydrogen bonding interactions between the nucleating agent and PA6.In this study,a hydroxyl-containing amidebased nucleating agent,BHT,was designed and synthesized using a tyramine-based biomass as the raw material.These results demonstrated that BHT exhibited good structural compatibility with PA6.After adding 1 wt%BHT,the crystallization temperature of PA6 increased from 170.9℃to 193.3℃,the crystallinity increased 16.6%,the heat distortion temperature and Vicat softening temperature rose to 89.5 and 187.8℃,respectively,the haze decreased to 46%,achieving the synergistic optimization of mechanical,thermal,and optical properties.The in situ time-resolved FTIR results indicated that the addition of BHT increased the enthalpy of hydrogen bond formation during the nucleation stage,facilitated the segmental conformation adjustment of PA6,and enhanced the molar concentration of trans-conformations,ultimately leading to an improvement in the crystallization rate.展开更多
A diamine containing ether and ester units, as basic monomer for the preparation of polyamides, was prepared via three consecutive reactions. Nucleophilic substitution reaction of 1,4-dihydroxy benzene with 4-nitroben...A diamine containing ether and ester units, as basic monomer for the preparation of polyamides, was prepared via three consecutive reactions. Nucleophilic substitution reaction of 1,4-dihydroxy benzene with 4-nitrobenzoyl chloride produced 4-hydroxyphenyl 4-nitrobenzoate （HPNB）. Reduction of nitro groups to amino groups using Fe and HC1 resulted in preparation of 4-hydroxyphenyl 4-aminobenzoate （HPAB）. The diamine was synthesized through nucleophilic substitution reaction of HPAB with 2,6-dichloropyridine. The precursors and diamine were fully characterized by common methods, and the diamine was polycondensed with different diacid chlorides in the presence of an acid scavenger to prepare new polyamides. The polyamides were characterized, and their physical properties including thermal stability and behavior, inherent viscosity and solubility were studied.展开更多
Long chain semiaromatic polyamides with high molecular weight were synthesized by the reactions of undecanediamine with various aromatic diacids,and characterized by fourier transform infrared spectra（FT-IR） and nuc...Long chain semiaromatic polyamides with high molecular weight were synthesized by the reactions of undecanediamine with various aromatic diacids,and characterized by fourier transform infrared spectra（FT-IR） and nuclear magnetic resonance（1H-NMR）.The thermal behaviors were determined by differential scanning calorimetry（DSC） and thermogravimetric analysis（TGA）.The solubility,dynamic mechanical,physical and mechanical properties of the polyamides were also investigated.The experimental results show that the polyamides with high molecular weights are obtained only the PH value of the polyamides salt are in the range of 7.2-7.4.The melting temperatures and the glass transition temperatures of the polyamides increase with the increase of the rigidity of aromatic diacids,and are near to those of poly（nonamethylenetere-phthalamide）（PA9T）.展开更多
Enabling thermoplastic polyamides with significant room temperature phosphorescent(RTP)performance holds great application potential,but remains challenging.Herein,we develop an efficient crystallization-mediated appr...Enabling thermoplastic polyamides with significant room temperature phosphorescent(RTP)performance holds great application potential,but remains challenging.Herein,we develop an efficient crystallization-mediated approach to fabricate RTP-active bio-based polyamide 56(PA56)that simultaneously achieves an exceptional phosphorescence lifetime of 1.214 s and maintains robust mechanical properties with a tensile yield strength exceeding 80 MPa.Comprehensive characterization demonstrates that the material's RTP characteristics can be precisely tuned through controlled crystallization,where the synergistic effects of electron-rich carbonyl group aggregation(functioning as phosphorescent centers)and interchain hydrogen-bonding networks effectively suppress non-radiative decay pathways.This crystallization-dependent modulation enables systematic optimization of PA56's phosphorescent properties.Furthermore,we successfully demonstrate practical applications leveraging these unique RTP features,including advanced information encryption/anti-counterfeiting systems and innovative visualization techniques for real-time moisture monitoring and mechanical load assessment in PA56 products.This work establishes a general design strategy for engineering thermoplastic polyamides with tailorable phosphorescence,opening new avenues for smart material development.展开更多
It is essential to design economic and efficient tougheners to prepare high-performance epoxy resin;however,this has remained a huge challenge.Herein,an eco-friendly,low-cost,and facile-fabricated bio-based hyperbranc...It is essential to design economic and efficient tougheners to prepare high-performance epoxy resin;however,this has remained a huge challenge.Herein,an eco-friendly,low-cost,and facile-fabricated bio-based hyperbranched toughener,carboxylic acid-functionalized tannic acid(CATA),was successfully prepared and applicated to the preparation of solvent-free epoxy resins.The mechanical performance,morphology,structural characterization,and thermal characterization of toughened epoxy resin system were studied.The toughened epoxy resin system with only 1.0wt%CATA reached the highest impact strength,111%higher than the neat epoxy resin system.Notably,the tensile strength and elongation at break of toughened epoxy resin systems increased moderately with increasing CATA loading.Nonphase-separated hybrids with significant toughening effect were obtained.Additionally,the thermal stabilities of toughened epoxy resin systems decreased with increasing CATA loading.This study provides an eco-friendly,cost-effective,and facile approach for the preparation of high-performance,solvent-free epoxy resins with potential for practical applications in sealing integrated circuits and electrical devices fields.展开更多
Five new optically active polyamides （PAs） 6a-6e were prepared by direct polycondensation reaction of 2-（1,3- isoindolinedione-2-yl）-glutaric acid 4 as a new chiral diacid with various aromatic diamines 5a-Se in a...Five new optically active polyamides （PAs） 6a-6e were prepared by direct polycondensation reaction of 2-（1,3- isoindolinedione-2-yl）-glutaric acid 4 as a new chiral diacid with various aromatic diamines 5a-Se in a medium consisting of triphenyl phosphite （TPP）, calcium chloride, pyridine （Py） and N-methyl-2-pyrrolidone （NMP）. The polycondensation reaction produced a series of polyamids 6a-6e in quantitative yields with inherent viscosities of 0.26-0.39 dL/g. The resulting polymers were fully characterized by means of ^1H-NMR, FT-1R spectroscopy, elemental analysis, inherent viscosity and specific rotation. Thermal properties of these polymers were investigated using thermal gravimetric analysis （TGA） and differential thermal gravimetry （DTG）. Phthalimide rings as a bulky pendent group in the polymer chains disturb the interchain and intrachain interactions and make these PAs readily soluble in polar, aprotic solvents such as N,N-dimethyl acetamide （DMAc）, N,N-dimethyl formamide （DMF）, dimethyl sulfoxide （DMSO）, N-methyl-2-pyrrolidone （NMP） and sulfuric acid.展开更多
Long chain semiaromatic polyamides were synthesized by the reactions of decanediamine with various aromatic diacids and characterized by Fourier transform infrared spectroscopy （FT-IR） and nuclear magnetic resonance...Long chain semiaromatic polyamides were synthesized by the reactions of decanediamine with various aromatic diacids and characterized by Fourier transform infrared spectroscopy （FT-IR） and nuclear magnetic resonance （^1H-NMR）. The thermal behaviors were determined by differential scanning calorimetry （DSC） and thermogravimetric analysis （TGA）. The solubility, dynamic mechanical, physical and mechanical properties of the polyamides have also been investigated. The resultant polyamides have intrinsic viscosity ranging from 1.7 dL/g to 2.1 dL/g. Their melting temperatures range from 305℃ to 343℃, and the glass transition temperatures fall in the range of 125-130℃. The tensile strength of the polyamides is above 100 MPa.展开更多
基金support from the National Natural Science Foundation of China(Nos.22293011,T2341001)the Major Science and Technology Project of Anhui Province(202203a06020010).
文摘Epoxy resins are widely employed in wind turbine blades,drone rotors,and automotive interiors due to their excel-lent mechani-cal proper-ties and long service life.However,their insoluble and infusible cross-linked networks pose a significant re-cycling challenge,particularly with the impending retirement of the first generation of wind turbine blades.In this work,we reported a fully bio-based epoxy Vitrimer(FEP)incorporat-ing a dual-dynamic covalent network design and systematically investigated the influence of the 1,5,7-triazabicyclo[4.4.0]dec-5-ene(TBD)catalyst on its curing kinetics,thermal/mechan-ical properties,dynamic exchange behavior,and degradation performance in a mild alkaline solution.Compared to conventional epoxy resins,FEP exhibited superior tensile strength and elongation at break at an optimal TBD concentration(2 wt%),achieving an excellent strength-toughness balance.The presence of TBD accelerated the exchange rates of both disulfide and ester bonds,endowing FEP with notable stress relaxation at elevated tempera-tures.Moreover,FEP demonstrated complete dissolution in 1 mol/L NaOH within 6 h at 25℃.These results underscored the exceptional strength,toughness,and recyclability of FEP,positioning it as a promising,environmentally friendly matrix resin for next-generation appli-cations in the new energy sector.
基金supported by the National Natural Sci-ence Foundation of China(Nos.U21A20288 and 21978280).
文摘Developing green and efficient methods to acquire lignocellulose-based chemicals with high added value is beneficial for facilitating green chemistry and sustainable development.The goal of this study is to demonstrate that bio-based benzaldehyde,a noteworthy high-value chemical,is able to be directionally prepared from lignocellulosic biomass.This new control-lable transformation was materialized by uniting catalytic-pyrolysis of lignocellulose to toluene intermediate and catalytic oxidation of toluene intermediate to bio-based benzalde-hyde.This work also developed a highly active magnetic catalyst(CoFe_(2)O_(4)@Biochar(HTR)),achieving 77.1%benzaldehyde selectivity and 46.7%benzaldehyde yield using this catalyst.It was found that introducing the biochar carrier into the cobalt iron composite metal oxide cat-alyst enhanced hydroxyl radical formation and bio-based benzaldehyde synthesis.Based on catalyst characterizations and hydroxyl radical analysis,potential reaction mechanism for bio-based benzaldehyde synthesis was proposed.This strategy may provide a beneficial pathway for developing high-value bio-based chemical(benzaldehyde)using renewable lignocellulosic biomass.
基金National Key Research and Development Program of China(No.2017YFB0309400).
文摘This study aims to develop highly hygroscopic bio-based co-polyamides(CPs)by melt co-polycondensation of polyamide(PA)56 salt and PA66 salt with varying molar fractions.The functional groups and the chemical structure of the prepared samples were determined by Fourier transform infrared(FTIR)spectroscopy and proton nuclear magnetic resonance(^(1)H-NMR)spectroscopy.The relative viscosity was determined with an Ubbelohde viscometer.The melting behavior and the thermal stability of CPs were investigated by differential scanning calorimetry(DSC)and thermogravimetric analysis(TGA).Furthermore,the water absorption behavior of CP hot-pressed film was studied.The results reveal that the melting point,the crystallization temperature and the crystallinity of CPs firstly decrease and then increase with the molar fraction of PA66 in CPs.The copolymerization of PA56 with PA66 leads to an obvious increase in water absorption.The CPs with PA66 molar fraction of 50%possess a high saturated water absorption rate of 17.6%,compared to 11.6%for pure PA56 and 7.8%for pure PA66.
基金financially supported by the National Key Research and Development Program of China (Nos. 2017YFB0309301 and 2017YFB0309302)the Natural Science Foundation of Shanghai, China (No. 17ZR1407200)
文摘Novel bio-based and biodegradable block copolymers were synthesized by "click" reaction between poly(L-lactide)(PLLA) and polyamide 4(PA4). Upon tuning the molar mass of PLLA block, the properties of copolymers and electrospun ultrafine fibers were investigated and compared with those of PLLA and PA4 blends. PLLA and PA4 were found incompatible and formed individual crystalline regions, along with reciprocal inhibition in crystallization. Electrospun fibers were highly hydrophobic, even if hydrophilic PA4 was the rich component. The crystallinity of either PLLA or PA4 decreased after electrospinning and PLLA-rich as-spun fibers were almost amorphous. Immersion tests proved that fibers of block copolymers were relatively homogeneous with micro-phase separation between PLLA and PA4. The fibrous structures of copolymers were different from those of the fibers electrospun from blends, for which sheath-core structure induced by macro-phase separation between homopolymers of PLLA and PA4 was confirmed by TEM, EDS, and XPS.
基金This work was financially supported by the National Natural Science Foundation of China(No.51803224).
文摘The objective of this study was to improve the toughness of bio based brittle poly(ethylene 2,5-furandicarboxylate)(PEF)by melt blending with bio based polyamide11(PA11)in the presence of a reactive multifunctional epoxy compatibilizer(Joncryl ADR-4368).The morphological,thermal,rheological,and mechanical properties of PEF/PA11 blends were investigated.Compared with neat PEF,the toughness of PEF/PA11 blend was not improved in the absence of the reactive compatibilizer due to the poor compatibility between the two polymers.When Joncryl was incorporated into PEF/PA11 blends,the interfacial tension between PEF and PA11 was obviously reduced,reflecting in the fine average particle size and narrow distribution of PA11 dispersed phase as observed by scanning electron microscopy(SEM).The complex viscosities of PEF/PA11 blends with Joncryl were much higher than that of PEF/PA11 blend,which could be ascribed to the formation of graft copolymers through the epoxy groups of Joncryl reacting with the end groups of PEF and PA11 molecular chains.Thus,the compatibility and interfacial adhesion between PEF and PA11 were greatly improved in the presence of Joncryl.The compatibilized PEF/PA11 blend with 1.5 phr Joncryl exhibited significantly improved elongation at break and unnotch impact strength with values of 90.1%and 30.3kJ/m2,respectively,compared with those of 3.6%and 3.8 kJ/m2 for neat PEF,respectively.This work provides an effective approach to improve the toughness of PEF which may expand its widespread application in packaging.
基金supported by the Key R&D Project in Shaanxi Province(No.2024GX-YBXM-371)Shaanxi Qinchuangyuan Scientists+Engineers Team Construction Project(2025QCY-KXJ-141).
文摘With the escalating global emphasis on environmental conservation and sustainable development,enhancing the service quality and durability of road surfaces and facilitating the green development of highways have commanded considerable attention.Bio-based polyurethane,on account of its remarkable physical and chemical properties,green,sustainable and renewable capacity,as well as its structural design capabilities,has drawn widespread attention and numerous studies have been carried out.It has gradually started to substitute traditional petroleum-based polyurethane materials in road engineering.Nevertheless,the application of bio-based polyurethane materials in road engineering remains in the exploratory phase.To stimulate the application research of bio-based polyurethane materials in road engineering and offer additional research directions,this paper reviews the research advancements of bio-based polyurethane materials and their applications in road engineering.The fundamental classification of bio-based polyurethane is introduced.The characteristics and challenges associated with various preparation methods for bio-based polyurethane are described.The influence of bio-based polyurethane on road engineering materials are analyzed.The evaluation indicators of bio-based polyurethane within the life cycle of road engineering are investigated.Finally,the development tendency towards in road engineering applications are forecasted.This paper provides a reference for the study of bio-based polyurethane materials in road engineering applications.
基金supported by the Science and Technology Research Project of Henan Province(222102230031)Key Scientific Research Projects of Colleges and Universities in Henan Province(23A430018)Natural Science Foundation of Henan(252300420267).
文摘The current global shortage of oil resources and the pollution problems caused by traditional barrier materials urgently require the search for new substitutes.Biodegradable bio-based barrier materials possess the characteristics of being renewable,environmentally friendly,and having excellent barrier properties.They have become an important choice in fields such as food packaging,agricultural film covering,and medical protection.This review systematically analyzes the design and research of this type of material,classifying biobased and biodegradable barrier materials based on the sources of raw materials and synthesis pathways.It also provides a detailed introduction to the latest research progress of biobased and biodegradable barrier materials,discussing the synthesis methods and improvement measures of their barrier properties.Subsequently,it analyzes the related technologies for enhancing the barrier properties of biobased and biodegradable barrier materials,and finally looks forward to the directions that future research should focus on,promoting the transition of biobased and biodegradable barrier materials from the laboratory to industrial applications.
基金supported by the China Postdoctoral Science Foundation(No.2023M743622)Natural Science Foundation of Ningbo City(No.2024J109)+2 种基金National Natural Science Foundation of China(Nos.E52307038 and U23A20589)Ningbo 2025 Key Scientific Research Programs(Nos.2022Z111,2022Z160 and 2022Z198)the Leading Innovativeand Entrepreneur Team Introduction Program of Zhejiang(No.2021R01005).
文摘The demand for energy-efficient and environmental-friendly power grid construction has made the exploitation of bio-based electrical epoxy resins with excellent properties increasingly important.This work developed the bio-based electrotechnical epoxy resins based on magnolol.High-performance epoxy resin(DGEMT)with a double crosslinked points and its composites(Al_(2)O_(3)/DGEMT)were obtained taking advantages of the two bifunctional groups(allyl and phenolic hydroxyl groups)of magnolol.Benefitting from the distinctive structure of DGEMT,the Al_(2)O_(3)/DGEMT composites exhibited the advantages of intrinsically high thermal conductivity,high insulation,and low dielectric loss.The AC breakdown strength and thermal conductivity of Al_(2)O_(3)/DGEMT composites were 35.5 kV/mm and 1.19 W·m-1·K-1,respectively,which were 15.6%and 52.6%higher than those of petroleum-based composites(Al_(2)O_(3)/DGEBA).And its dielectric loss tanδ=0.0046 was 20.7%lower than that of Al_(2)O_(3)/DGEBA.Furthermore,the mechanical,thermal and processing properties of Al_(2)O_(3)/DGEMT are fully comparable to those of Al_(2)O_(3)/DGEBA.This work confirms the feasibility of manufacturing environmentally friendly power equipment using bio-based epoxy resins,which has excellent engineering applications.
文摘By investigating the performance characteristics of the bio-based surfactant 8901A,a composite decontamination and injection system was developed using 8901A as the primary agent,tailored for application in low-permeability and heavy oil reservoirs under varying temperature conditions.The results demonstrate that this system effectively reduces oil–water interfacial tension,achieving an ultra-low interfacial tension state.The static oil washing efficiency of oil sands exceeds 85%,the average pressure reduction rate reaches 21.55%,and the oil recovery rate improves by 13.54%.These enhancements significantly increase the system’s ability to dissolve oilbased blockages,thereby lowering water injection pressure caused by organic fouling,increasing the injection volume of injection wells,and ultimately improving oil recovery efficiency.
文摘Aging plays a critical role in determining the durability and long-term performance of asphalt pavements,as it is influenced by both external factors(e.g.,temperature,ultraviolet(UV)radiation,moisture,oxidative gases)and internal factors such as binder composition.Although laboratory simulations of aging are well established for conventional bituminous binders,limited attention has been paid to replicating and evaluating aging processes in bio-based binders.This review provides a comprehensive analysis of current laboratory techniques for simulating and assessing binder aging,with a focus on two key areas:aging simulation protocols and evaluation methodologies.The analysis shows that although several efforts have been made to incorporate external aging factors into lab simulations,significant challenges persist,especially in the case of bio-based binders,which are characterized by a high variability in composition and limited understanding of their aging behavior.Current evaluation approaches also exhibit limitations.Improvements are needed in the molecular-level analysis of oxidation(e.g.,through more representative oxidation modelsin molecular dynamicssimulations),in the separation and quantification of binder constituents,and in the application of advanced techniques such as fluorescence microscopy to better characterize polymer dispersion.To enhance the reliability of laboratory simulations,future research should aim to improve the correlation between laboratory and field aging,define robust aging indexes,and refine characterization methods.These advancements are particularly critical for bio-based binders,whose performance is highly sensitive to aging and for which standard test protocols are still underdeveloped.A deeper understanding of aging mechanisms in both polymer-modified and biobased binders,along with improved analytical tools for assessing oxidative degradation and morphological changes,will be essential to support the development of sustainable,high-performance paving materials.
文摘In the context of transitioning toward more sustainable construction materials,this study explores the impact of incorporating millet husks as an alternative to sand on the physical,mechanical,and thermal performance of lightweight concrete.Through a mixture design approach,five formulations were selected and thoroughly characterized.The analysis of iso-response curves enabled an in-depth assessment of the cross-effects between formulation parameters and their interactions on the final properties of the material.The results show that integrating millet husks leads to a significant reduction in density,reaching up to 21%,while maintaining notable mechanical performance.A balanced formulation of sand and fibers achieved a maximum compressive strength of 12.11 MPa,demonstrating that,under specific conditions,plant fibers actively contribute to the structural integrity of the composite.In tensile strength,the positive influence of fibers is even more pronounced,with a maximum resistance of 8.62 MPa,highlighting their role in enhancing material cohesion.From a thermal perspective,millet husks reduce both thermal conductivity and effusivity,thereby limiting heat transfer and accumulation within the composite.Iso-response curve analysis reveals that these effects are directly linked to the proportions of the constituents and that achieving an optimal balance between sand,fibers,and cement is key to maximizing performance.These findings demonstrate that the adopted approach allows moving beyond conventional substitution methods by identifying optimal configurations for the design of lightweight bio-based concretes that are both strong and insulating,thereby confirming the potential of millet husks in developing lightweight concretes suitable for sustainable construction applications.
文摘An efficient and novel approach is proposed for oxidative arylation of bio-based furfuryl alcohol(FA)to aryl furans(AFs),a versatile monomer of photoelectric materials,in the presence of UiO-67-Pd(F)with phenanthroline/bipyridine,and poly-F substituted phenyl ligands as the mixture linkers.The results of control experiments and theoretical calculations reveal that the–F on the phenyl linkers efficiently tunes the electron-deficient nature of Pd through the Zr_(6) clusters bridges,which favors the adsorption and activation of the furan ring.Furthermore,the conjugation of different nitrogen-containing ligands facilitates Pd coordination for the Heck-type insertion and subsequent electrophilic palladation,respectively.As a result,the oxidative arylation of FA derivatives is substantially enhanced because of these electronic and steric synergistic effects.Under the optimized conditions,72.2%FA conversion and 74.8%mono aryl furan(MAF)selectivity are shown in the Heck-type insertion.Meanwhile,85.3%of MAF is converted,affording 74.8%selectivity of final product(AFs)in the subsequent electrophilic palladation reaction.This process efficiency is remarkably higher than that with homogeneous catalysts.In addition,furan-benzene polymer obtained from the halogen-free synthesis catalyzed by UiO-67-Pd(F)show significantly better properties than that from conventional Suzuki coupling method.Therefore,the present work provides a new insight for useful AFs synthesis by oxidative arylation of bio-furan via rational tunning the metal center micro-environment of heterogeneous catalyst.
基金the National Natural Science Foundation of China (Nos.52430001,52470091,52200108) for the financial support。
文摘Nanofiltration(NF) technology,with its capacity for nanoscale filtration and controllable selectivity,holds significant promise in diverse applications.However,the current upper bound of permeance and selectivity of NF membranes is intrinsically constrained by the morphology and structure of the polyamide(PA) selective layer.This issue arises because NF membranes typically exhibit relatively smooth nodular structures,which theoretically impede efficient water transport.In this study,we enhanced the formation of nanobubbles by synergistically regulating with surfactant and low temperatures,resulting in the fabrication of PA NF membranes with a crumpled morphology.We observed that lower temperatures promote enhanced gas solubility in the aqueous phase,facilitating increased nanobubble formation through the foaming effect of surfactant sodium dodecylbenzene sulfonate(SDBS).Consequently,this resulted in the creation of PA NF membranes with more crumpled structures and superior performance,with pure water permeance reaching 36.25 ± 0.42 L m^(-2)h^(-1)bar^(-1),representing an improvement of 14.47 L m^(-2)h^(-1)bar^(-1)compared to the control group.Additionally,it maintains a high Na_(2)SO_(4) rejection rate of97.00 % ± 0.58 %.The PA NF membranes produced by eliminating nanobubbles and free interfaces exhibited a smooth structure,whereas introducing nanobubbles(through Na HCO_(3) addition,N_(2) pressurization,and ultrasonication) resulted in the formation of crumpled membranes.This emphasized that the large amount of nanobubbles generated by SDBS and low temperature in the interfacial process played a critical role in shaping crumpled PA NF membranes and enhancing membrane performance.This approach has the potential to provide valuable insights into customizing the structural design of TFC PA NF membranes,contributing to further advancements in this field.
文摘The chemical structure of polyamide 6(PA6)dictates that only 50%of hydrogen bonds participate in crystallization during the crystallization process,resulting in the properties of its products being significantly dependent on the molding process.Therefore,the design and development of nucleating agents suitable for PA6 holds great practical significance for high-performance PA6 materials.Amide-based nucleating agents can effectively improve the crystallization rate by increasing intermolecular hydrogen bond density.Further introduction of hydroxyl groups can enhance the hydrogen bonding interactions between the nucleating agent and PA6.In this study,a hydroxyl-containing amidebased nucleating agent,BHT,was designed and synthesized using a tyramine-based biomass as the raw material.These results demonstrated that BHT exhibited good structural compatibility with PA6.After adding 1 wt%BHT,the crystallization temperature of PA6 increased from 170.9℃to 193.3℃,the crystallinity increased 16.6%,the heat distortion temperature and Vicat softening temperature rose to 89.5 and 187.8℃,respectively,the haze decreased to 46%,achieving the synergistic optimization of mechanical,thermal,and optical properties.The in situ time-resolved FTIR results indicated that the addition of BHT increased the enthalpy of hydrogen bond formation during the nucleation stage,facilitated the segmental conformation adjustment of PA6,and enhanced the molar concentration of trans-conformations,ultimately leading to an improvement in the crystallization rate.
文摘A diamine containing ether and ester units, as basic monomer for the preparation of polyamides, was prepared via three consecutive reactions. Nucleophilic substitution reaction of 1,4-dihydroxy benzene with 4-nitrobenzoyl chloride produced 4-hydroxyphenyl 4-nitrobenzoate （HPNB）. Reduction of nitro groups to amino groups using Fe and HC1 resulted in preparation of 4-hydroxyphenyl 4-aminobenzoate （HPAB）. The diamine was synthesized through nucleophilic substitution reaction of HPAB with 2,6-dichloropyridine. The precursors and diamine were fully characterized by common methods, and the diamine was polycondensed with different diacid chlorides in the presence of an acid scavenger to prepare new polyamides. The polyamides were characterized, and their physical properties including thermal stability and behavior, inherent viscosity and solubility were studied.
文摘Long chain semiaromatic polyamides with high molecular weight were synthesized by the reactions of undecanediamine with various aromatic diacids,and characterized by fourier transform infrared spectra（FT-IR） and nuclear magnetic resonance（1H-NMR）.The thermal behaviors were determined by differential scanning calorimetry（DSC） and thermogravimetric analysis（TGA）.The solubility,dynamic mechanical,physical and mechanical properties of the polyamides were also investigated.The experimental results show that the polyamides with high molecular weights are obtained only the PH value of the polyamides salt are in the range of 7.2-7.4.The melting temperatures and the glass transition temperatures of the polyamides increase with the increase of the rigidity of aromatic diacids,and are near to those of poly（nonamethylenetere-phthalamide）（PA9T）.
基金supported by the Young Elite Scientists Sponsorship Program by Beijing Association for Science and Technology(BAST)(BYESS2023086)the Fundamental Research Funds for the Central Universities(buctrc202225)the Scientific Research Projects of China National Petroleum Corporation(PRIKY23093)。
文摘Enabling thermoplastic polyamides with significant room temperature phosphorescent(RTP)performance holds great application potential,but remains challenging.Herein,we develop an efficient crystallization-mediated approach to fabricate RTP-active bio-based polyamide 56(PA56)that simultaneously achieves an exceptional phosphorescence lifetime of 1.214 s and maintains robust mechanical properties with a tensile yield strength exceeding 80 MPa.Comprehensive characterization demonstrates that the material's RTP characteristics can be precisely tuned through controlled crystallization,where the synergistic effects of electron-rich carbonyl group aggregation(functioning as phosphorescent centers)and interchain hydrogen-bonding networks effectively suppress non-radiative decay pathways.This crystallization-dependent modulation enables systematic optimization of PA56's phosphorescent properties.Furthermore,we successfully demonstrate practical applications leveraging these unique RTP features,including advanced information encryption/anti-counterfeiting systems and innovative visualization techniques for real-time moisture monitoring and mechanical load assessment in PA56 products.This work establishes a general design strategy for engineering thermoplastic polyamides with tailorable phosphorescence,opening new avenues for smart material development.
基金from the Special Fund for the Program for Zhejiang Provincial Natural Science Foundation of China(LZ16C160001)National Key Research and Development Program(2017YFD0601105),the National Natural Science Foundation of China(Grant No.21806142)the Zhejiang Provincial Natural Science Foundation of China(Grant No.LY20B070002).
文摘It is essential to design economic and efficient tougheners to prepare high-performance epoxy resin;however,this has remained a huge challenge.Herein,an eco-friendly,low-cost,and facile-fabricated bio-based hyperbranched toughener,carboxylic acid-functionalized tannic acid(CATA),was successfully prepared and applicated to the preparation of solvent-free epoxy resins.The mechanical performance,morphology,structural characterization,and thermal characterization of toughened epoxy resin system were studied.The toughened epoxy resin system with only 1.0wt%CATA reached the highest impact strength,111%higher than the neat epoxy resin system.Notably,the tensile strength and elongation at break of toughened epoxy resin systems increased moderately with increasing CATA loading.Nonphase-separated hybrids with significant toughening effect were obtained.Additionally,the thermal stabilities of toughened epoxy resin systems decreased with increasing CATA loading.This study provides an eco-friendly,cost-effective,and facile approach for the preparation of high-performance,solvent-free epoxy resins with potential for practical applications in sealing integrated circuits and electrical devices fields.
文摘Five new optically active polyamides （PAs） 6a-6e were prepared by direct polycondensation reaction of 2-（1,3- isoindolinedione-2-yl）-glutaric acid 4 as a new chiral diacid with various aromatic diamines 5a-Se in a medium consisting of triphenyl phosphite （TPP）, calcium chloride, pyridine （Py） and N-methyl-2-pyrrolidone （NMP）. The polycondensation reaction produced a series of polyamids 6a-6e in quantitative yields with inherent viscosities of 0.26-0.39 dL/g. The resulting polymers were fully characterized by means of ^1H-NMR, FT-1R spectroscopy, elemental analysis, inherent viscosity and specific rotation. Thermal properties of these polymers were investigated using thermal gravimetric analysis （TGA） and differential thermal gravimetry （DTG）. Phthalimide rings as a bulky pendent group in the polymer chains disturb the interchain and intrachain interactions and make these PAs readily soluble in polar, aprotic solvents such as N,N-dimethyl acetamide （DMAc）, N,N-dimethyl formamide （DMF）, dimethyl sulfoxide （DMSO）, N-methyl-2-pyrrolidone （NMP） and sulfuric acid.
文摘Long chain semiaromatic polyamides were synthesized by the reactions of decanediamine with various aromatic diacids and characterized by Fourier transform infrared spectroscopy （FT-IR） and nuclear magnetic resonance （^1H-NMR）. The thermal behaviors were determined by differential scanning calorimetry （DSC） and thermogravimetric analysis （TGA）. The solubility, dynamic mechanical, physical and mechanical properties of the polyamides have also been investigated. The resultant polyamides have intrinsic viscosity ranging from 1.7 dL/g to 2.1 dL/g. Their melting temperatures range from 305℃ to 343℃, and the glass transition temperatures fall in the range of 125-130℃. The tensile strength of the polyamides is above 100 MPa.
