In this study,a facile method was employed to synthesize strong,yet highly elastic polyurethane-urea(PUU)with typical characteristics and 94% optical transmittance.Graphene platelets(GNPs)were prepared and modified vi...In this study,a facile method was employed to synthesize strong,yet highly elastic polyurethane-urea(PUU)with typical characteristics and 94% optical transmittance.Graphene platelets(GNPs)were prepared and modified via a scalable and eco-friendly mechanochemical approach.The produced GNPs is at 1.6-nm thickness with high electrical conductivity of~950 S/m.The structure-property relations of PUU/GNP nanocomposites were comprehensively investigated through morphology and mechanical properties measurements.The strong interface and high-density hydrogen bonds between modified GNPs(M-GNPs)and PUU significantly enhanced the mechanical properties of the PUU nanocomposite.The PUU composite showed 66.7%and 36.2%increments in tensile and impact strengths,respectively,at 0.2 wt% M-GNPs.The reversible hydrogen bond between M-GNPs and PUU endowed the nanocomposite with self-healing properties achieving 97.8% healing efficiency of the strength after 5 h at 120℃.This study demonstrates the importance of surface modification and provides a simple yet robust approach for preparing high-performance and functional PUU/graphene composites.展开更多
Azobenzene-based polymer actuators show great promise for photoactuation owing to their unique photoisomerization behavior and tailorable molecular programmability.However,conventional systems are limited by inadequat...Azobenzene-based polymer actuators show great promise for photoactuation owing to their unique photoisomerization behavior and tailorable molecular programmability.However,conventional systems are limited by inadequate mechanical robustness,self-healing,and recyclability,hindering their practical implementation.Herein,we present a high-performance azobenzene-functionalized polyurethane(AzoPU)elastomer actuator designed via molecular engineering of photoactive azobenzene moieties and dynamic disulfide bonds.AzoPU exhibits exceptional mechanical properties with retained performance after multiple reshaping cycles,enabled by well-engineered hard-soft segments and synergistic stress dissipation from weak covalent bonds/hierarchical hydrogen bonds.It achieves over 93%self-healing efficiency at room temperature owing to the synergistic interplay of disulfide bonds in the polymer backbone and intermolecular hydrogen bonds.Furthermore,it demonstrates remarkable light-triggered actuation behavior,achieving a phototropic bending angle exceeding 180°toward the light source within 45 s.To showcase its practical potential,proof-of-concept photoactuated devices with flower-,hook-,and gripper-like and local-orientation processed strip-shaped structures were fabricated,which exhibited rapid and reversible light-triggered deformation.This study proposes a novel strategy for the development of intelligent polymeric materials that integrate light responsiveness,self-healing,and recyclability,thus holding great promise for applications in flexible electronics,smart actuators,and sustainable functional materials.展开更多
Recent advancements in developing tannin-based non-isocyanate polyurethane(NIPU)resins have unlocked new possibilities for sustainable and eco-friendly wood adhesives.Unlike conventional polyurethane,NIPUs eliminate h...Recent advancements in developing tannin-based non-isocyanate polyurethane(NIPU)resins have unlocked new possibilities for sustainable and eco-friendly wood adhesives.Unlike conventional polyurethane,NIPUs eliminate hazardous isocyanates,offering safer alternatives for industrial applications.Tannin,a naturally occurring polyphenolic compound,plays a pivotal role in enhancing these resins’fire-resistance and super-hydrophobic properties.This review highlights key developments in synthesizing tannin-based NIPU,focusing on various polymerization techniques such as polyaddition,polycondensation,ring-opening polymerization,and rearrangement.These strategies contribute to improved mechanical strength,thermal stability,and resistance to water absorption.Recent studies demonstrate that tannin-based NIPU adhesives meet or exceed international internal bonding strength,elasticity,and durability standards.Their application in wood-based composites like oriented strand boards(OSB)has shown promising results,offering improved resistance to moisture and superior dimensional stability.Furthermore,the cross-linked polymer network,supported by chemical modifications like the introduction of fluoroalkyl groups,significantly enhances hydrophobicity and fire retardancy.Despite these advancements,challenges remain in terms of scalability,cost,and integration with existing manufacturing processes.Future research should focus on optimizing reaction conditions,improving raw material availability,and developing industrial-scale production methods.This review underscores the potential of tannin-based NIPU resins as a viable and sustainable alternative for various wood composite applications.展开更多
Polyurethane elastomers exhibit high dielectric constants owing to their polar groups,and can be used as energy storage capacitors.Energy storage depends not only on the dielectric constant but also on the dielectric ...Polyurethane elastomers exhibit high dielectric constants owing to their polar groups,and can be used as energy storage capacitors.Energy storage depends not only on the dielectric constant but also on the dielectric loss.However,the relationship between chain structure and dielectric properties is not yet clear.Ketal-containing crosslinked polyurethane elastomers were prepared using cyclic ketal diol as a chain extender.The effect of the soft segment length on the dielectric properties and energy storage was investigated.The cause of the change in the dipolar polarization with the soft segment length was analyzed.As the soft segment length increased,the hard-soft hydrogen bonding decreased,whereas the hard-hard hydrogen bonding increased.Under the action of an electric field,the polar bonds in the ketal-containing polyurethane elastomer overcome the hydrogen bonding between hard-soft segments to produce polarization;meanwhile,they also experience crankshaft motions to generate polarization.The former has a relatively high relaxation activation energy of approximately 10-20 k J·mol^(-1),resulting in a large dielectric loss.The latter has a relatively low relaxation activation energy,approximately 0.7-1.7 kJ·mol^(-1),leading to low dielectric loss.As a result,the dielectric constant showed a decreasing trend,and the dielectric loss gradually decreased.This study provides a theoretical foundation for improving the dielectric properties of polyurethane elastomers.展开更多
Near-infrared(NIR)light-responsive shape memory polymers(SMPs)show great promise for biomedical applications,but conventional photothermal agents suffer from high cost,complex preparation,or poor biocompatibility,whil...Near-infrared(NIR)light-responsive shape memory polymers(SMPs)show great promise for biomedical applications,but conventional photothermal agents suffer from high cost,complex preparation,or poor biocompatibility,while lignin-based alternatives exhibit insufficient photothermal conversion efficiency.Herein,we developed a novel strategy to enhance photothermal performance of lignin through sequential demethylation modification and Fe^(3+)complexation for constructing NIR light responsive SMPs.Dealkaline lignin(DL)was first demethylated using iodocyclohexane to produce demethylated lignin(DDL)with increased catechol content,which was then incorporated into polycaprolactone-based polyurethane synthesis followed by Fe^(3+)complexation.Results showed that DDL-Fe^(3+)complexes have significantly enhanced photothermal conversion performance,and the resulting PU-DDL+Fe^(3+)polyurethane with 0.5 wt%DDL content demonstrated a temperature increases of 39.8℃under 0.33 W·cm-2808 nm NIR irradiation.This excellent photothermal performance enables the shape-fixed PU-DDL+Fe^(3+)polyurethane to rapidly recover to its initial shape under NIR light irradiation.Additionally,PU-DDL+Fe^(3+)polyurethane exhibits good mechanical properties and biocompatibility,demonstrating significant biomedical application potential.展开更多
The development of intrinsically conductive piezoresistive sensors with high strain tolerance has garnered significant interest.While elastomeric polymers exhibit excellent strain capabilities,their utility in sensing...The development of intrinsically conductive piezoresistive sensors with high strain tolerance has garnered significant interest.While elastomeric polymers exhibit excellent strain capabilities,their utility in sensing applications has been limited by inherent challenges such as high electrical resistivity,poor aging resistance,and interfacial incompatibility.To address these limitations,hydroxyl-terminated polybutadiene(HTPB)-based polyurethane was chemically modified with acetylferrocene-polyaniline conductive moieties to enhance charge transport properties.Remarkably,this covalent functionalization endowed the resulting ferrocene-polyaniline hybrid polyurethane(FPHP)with a conductivity of2.33 n A at 1 V bias while preserving piezoresistive functionality.The FPHP demonstrated exceptional mechanical-electrical performance,achieving 254% elongation at break with strain-dependent gauge factors of 7.28(0%-12.5% strain,R^(2)=0.9504)and 19.66(12.5%-35.0% strain,R^(2)=0.9929).Further characterization revealed a rapid 0.60 s response time and stability over 3500 strain-release cycles at compression strain,underscoring its durability under repetitive loading.The FPHP sensor was capable of monitoring various human movements and recognizing writing signals.These advances establish a materials design paradigm for fabricating flexible sensors that synergistically integrate high deformability,tunable sensitivity,and robust operational stability,positioning FPHP as a promising candidate for next-generation wearable electronics and soft robotics.展开更多
Pyrolysis technology has emerged as a promising method for converting waste polyurethane(WPU)from waste refrigerators into high-value chemicals.In this study,the copper(Cu)-assisted pyrolysis strategy was employed to ...Pyrolysis technology has emerged as a promising method for converting waste polyurethane(WPU)from waste refrigerators into high-value chemicals.In this study,the copper(Cu)-assisted pyrolysis strategy was employed to enhance the thermal degradation efficiency and product quality of WPU.Kinetic analysis revealed that the activation energy(E_(a)) of the Cu-assisted pyrolysis was 136.64 kJ·mol^(−1) and Cu-assisted pyrolysis was controlled by the combined processes of diffusion,nucleation and phase boundary reactions.Comprehensive product analysis,including gas chromatography–mass spectrometry and thermogravimetric Fourier transform infrared spectroscopy–mass spectrometry suggested that Cu promoted the cleavage of urethane bonds and accelerated the decarboxylation of isocyanates,increasing the yields of aniline and ethanol at lower temperatures.Meanwhile,Cu effectively suppressed the formation of halogenated and heterocyclic compounds by promoting the cleavage of C–X(X=Cl,F)bonds through electron transfer interactions.Thus,the E_(a) is decreased and the halogenated compounds is reduced.This work provides the theoretical basis for converting waste to high-valued products through co-pyrolysis techniques.展开更多
In view of the problems such as the low utilization efficiency of copper tailings solid waste,which leads to severe environmental pollution,and the easy combustibility of rigid polyurethane foam(RPUF)along with the ge...In view of the problems such as the low utilization efficiency of copper tailings solid waste,which leads to severe environmental pollution,and the easy combustibility of rigid polyurethane foam(RPUF)along with the generation of a large amount of toxic smoke during combustion,copper tailings were combined with melamine polyphosphate to prepare RPUF composites.The flame-retardant properties were investigated,and the structure–property relationship was clarified.It was found that when 16.7 g of copper tailings and 33.3 g of melamine polyphosphate were added,the limiting oxygen index increased to 23.0 vol.%,and the vertical burning rating(UL-94)reached V-0.The peak heat release rate was reduced by 27.79%compared to pure RPUF,and the fire growth index decreased to 4.54 kW/(m^(2)s),representing a 75.42%reduction.The char residue rate at 750℃ increased from 17.6% to 28.51%.Moreover,the addition of copper tailings and melamine polyphosphate effectively promoted the charring of RPUF,forming a dense char layer with good fire resistance performance.展开更多
Airless tires are essential for enhancing the safety,reliability,and convenience of maintenance of electric bicycles.Polyurethane(PU)is considered a promising candidate for such applications owing to its versatile pro...Airless tires are essential for enhancing the safety,reliability,and convenience of maintenance of electric bicycles.Polyurethane(PU)is considered a promising candidate for such applications owing to its versatile properties.However,their use is limited by insufficient heat resistance and excessive dynamic heat generation under cyclic loading.In this study,star-shaped trifunctional polypropylene glycerol(PPG3)was incorporated into conventional poly(tetramethylene glycol)(PTMG)and 4,4'-methylenediphenyl diisocyanate(MDI)-based systems to construct microporous star-shaped casting polyurethanes(SCPU),with water serving as a green foaming agent.Unlike conventional small-molecule trifunctional crosslinkers that create junctions within hard segment domains,PPG3 introduces long flexible arms between the hard segments,anchoring the crosslinking points at its molecular core.The large steric hindrance of PPG3 effectively suppresses soft segment crystallization and lowers the degree of microphase separation,whereas the crosslinked network restricts chain mobility,thereby reducing dynamic heat generation.These structural features also enhance the heat resistance,yielding a softening temperature of 183℃,which is 30.9%higher than that of polyurethane without PPG3.When applied to airless tires by casting SCPU into rubber treads,the fabricated hybrid airless tires achieved a rolling distance of over 3000 km under a load of 65 kg at 25km/h without structural failure,satisfying practical performance requirements.This strategy offers a simple,solvent-free,and environmentally friendly process,underscoring the potential of SCPU for scalable production of high-performance airless tires.展开更多
Background:The development of materials for cardiovascular surgery that would improve the effectiveness of surgical interventions remains an important task.Surgical intervention during the implantation of vascular pro...Background:The development of materials for cardiovascular surgery that would improve the effectiveness of surgical interventions remains an important task.Surgical intervention during the implantation of vascular prostheses and stents,and the body’s reaction to artificial materials,could lead to chronic inflammation,a local increase in the concentration of proinflammatory factors,and stimulation of unwanted tissue growth.The introduction of nonsteroidal anti-inflammatory drugs into implantable devices could be used to obtain vascular implants that do not induce inflammation and do not induce neointimal tissue outgrowth.Methods:The scaffolds were made by electrospinning from mixtures of polyurethane(PU)with diclofenac(DF).The kinetics of DF release from the scaffolds composed of 3%PU/10%HSA/3%DMSO/DF and 3%PU/DF were studied.The biocompatibility and anti-inflammatory effects of the obtained scaffolds on human gingival fibroblasts and umbilical vein endothelial cells were studied.Results:Both types of scaffolds are characterized by fast DF release.The viability of cells cultured on scaffolds is 2 times worse than that of cells cultured on plastic.The level of the proinflammatory cytokine IL-6 in the culture medium of cells cultured on DF-containing scaffolds was lower than that of cells cultured on scaffolds without DF.Conclusion:The introduction of DF into scaffolds minimizes the inflammation caused by cell reactions to an artificial material.展开更多
This study aimed to systematically regulate the performance of 4D printing composites by investigating the synergistic effects of dicumyl peroxide(DCP)and maleic anhydride-grafted polyethylene(MAH-g-PE)on a poly(lacti...This study aimed to systematically regulate the performance of 4D printing composites by investigating the synergistic effects of dicumyl peroxide(DCP)and maleic anhydride-grafted polyethylene(MAH-g-PE)on a poly(lactic acid)/thermoplastic polyurethane(PLA/TPU)matrix.Specifically,using a 70 wt%/30 wt%PLA/TPU matrix and an L_(9)(3^(2))orthogonal design,composites were evaluated via morphology,shape memory,mechanical tests,and multi-criteria analysis.Moderate DCP enhanced crosslinking,improving storage modulus and thermal stability,while excessive DCP caused brittleness.Furthermore,MAH-g-PE effectively improved interfacial compatibility,and its synergy with DCP was dosage-dependent.Consequently,Sample 5 achieved optimal performance,exhibiting uniform fracture morphology,a shape fixation rate of98.8%with the fastest recovery,and balanced strength-ductility.Multi-criteria analysis identified elongation at break and recovery time as the top contributing factors,with consistent rankings validated by Spearman analysis(ρ=0.833,p<0.01).In summary,adjusting DCP and MAH-g-PE contents effectively modulates the crosslinking structure and interfacial properties of PLA/TPU composites,providing a viable strategy for developing high-performance,tunable 4D printing materials.展开更多
A polyacrylate/polyurethane (P(A)/P(U)) composite coating has been prepared by crosslinking an acetoacetylated polyacrylate with a vinylic group terminated polyurethane at room temperature. A model Michael reaction be...A polyacrylate/polyurethane (P(A)/P(U)) composite coating has been prepared by crosslinking an acetoacetylated polyacrylate with a vinylic group terminated polyurethane at room temperature. A model Michael reaction between ethyl acetoacetate (EAA) and methyl acrylate (MA) was designed to study the crosslinking mechanism. It was found that the two active hydrogen atoms in acetoacetyl group can both add to vinylic groups and the yield of mono-and bis-adducts are much affected by the molar ratio of acetoacetyl to vinylic groups. Higher crosslinking degree and better properties could be obtained with decreasing the molar ratio of the two active groups from 1/1 to 0.6/1 in the composite coatings.展开更多
Developing advanced ion-conductive networks is crucial for anion exchange membranes(AEMs).A flexible molecular structure facilitates the formation of ion clusters,resulting in enhanced ionic conductivity.Polyacrylates...Developing advanced ion-conductive networks is crucial for anion exchange membranes(AEMs).A flexible molecular structure facilitates the formation of ion clusters,resulting in enhanced ionic conductivity.Polyacrylates,known for their outstanding flexibility and chemical stability,hold significant potential as polymer electrolyte membranes.In this work,we innovatively constructed a series of polyacrylate-based AEMs decorated with pendant zwitterions(designated as PSBPA-X,BSBPA-X,where X=20,30,40).Specifically,the spacer length between the zwitterions is strategically optimized to enhance the ionic conductivity.Atomic force microscopy reveals that a longer spacer length between the zwitterions promotes the microphase separation and the formation of advanced water channels,which facilitates the OH^(-)transport in the BSBPA-40 membrane.Moreover,the stronger electrostatic potential and lower interaction energy between the BSBPA-40 and OH^(-)further contribute to efficient OH^(-)hopping transmission.Consequently,the BSBPA-40 membrane demonstrates the highest OH^(-)conductivity,achieving 102.1 mS cm^(-1)at 80℃ and 90% relative humidity,significantly surpassing that of the PSBPA-40 membrane(75.2 mS cm^(-1)).Additionally,the BSBPA-40 membrane exhibits remarkable flexibility with an improved breaking elongation of 480.5%due to the ionic cross-linking between the zwitterions.Notably,the BSBPA-40 membrane-based zinc-air battery achieves an outstanding power density of 156.7 mW cm^(-2)at room temperature,while its water electrolysis performance reaches 2.1 A cm^(-2)at 2.0 V.These results indicate that the developed membranes hold great promise for applications in sustainable and clean energy technologies.展开更多
Polyurethane foam,when used as a compressible layer in deep soft rock tunnels,offers a feasible solution to reduce the support pressure on the secondary lining.The foam spraying method using sprayed polyurethane mater...Polyurethane foam,when used as a compressible layer in deep soft rock tunnels,offers a feasible solution to reduce the support pressure on the secondary lining.The foam spraying method using sprayed polyurethane material is convenient for engineering applications;however,the compressive behaviour and feasibility of sprayed polyurethane material as a compressible layer remain unclear.To address this gap,this study conducts uniaxial compression tests and scanning electron microscope(SEM)tests to investigate the compressive behaviour of the rigid foams fabricated from a self-developed polyurethane spray material.A peridynamics model for the composite lining with a polyurethane compressible layer is then established.After validating the proposed method by comparison with two tests,a parametric study is carried out to investigate the damage evolution of the composite lining with a polyurethane compressible layer under various combinations of large deformations and compressible layer parameters.The results indicate that the polyurethane compressible layer effectively reduces the radial deformation and damage index of the secondary lining while increasing the damage susceptibility of the primary lining.The thickness of the polyurethane compressible layer significantly influences the prevention effect of large deformation-induced damage to the secondary lining within the density range of 50e100 kg/m^(3).In accordance with the experimental and simulation results,a simple,yet reasonable and convenient approach for determining the key parameters of the polyurethane compressible layer is proposed,along with a classification scheme for the parameters of the polyurethane compressible layer.展开更多
Bio-polyol is considered as a core material to synthesize eco-friendly polyurethane products.However,one of the popular bio-polyols,polytrimethylene ether glycol(PO3G),is reluctant to crystallize and therefore exhibit...Bio-polyol is considered as a core material to synthesize eco-friendly polyurethane products.However,one of the popular bio-polyols,polytrimethylene ether glycol(PO3G),is reluctant to crystallize and therefore exhibits a cold crystallization behavior.This abnormal behavior causes unstable mechanical properties at low-temperature and limits its applications in shape memory devices where crystallization is an essential mechanism.To analyze the unusual phenomenon,we compared different ether polyols focusing on symmetry characteristics and the evenodd effect of carbon backbones.It is found that PO3G has a slow crystallization rate because its ether linkages require specific chain arrangement for attractive interactions.Consequently,a thermal learning mechanism is developed to restore the normal crystallization behavior of elastomers synthesized from the bio-polyol.Repetitive heating and cooling cycles with high-temperature annealing induce urethane exchange reaction and reconstruct the chain orientations for fast crystallization.Results suggest the degree of crystallizations in polyurethane elastomer can be precisely controlled by introducing repetitive thermal treatments to enhance the potential applications of bio-polyols in polymer industries.展开更多
As a significant branch of smart materials,self-healing polyurethane materials mimic the biological damage repair mechanisms and have been widely applied in flexible electronics,functional coatings,biomedicine,and oth...As a significant branch of smart materials,self-healing polyurethane materials mimic the biological damage repair mechanisms and have been widely applied in flexible electronics,functional coatings,biomedicine,and other fields.This review systematically summarizes the design principles and recent advancements in both extrinsic and intrinsic self-healing polyurethane materials,highlighting their respective self-healing mechanisms and characteristics.For extrinsic system,damage repair is primarily achieved through microcapsules,hollow fibers,nanoparticles,and microvascular networks.However,their healing efficiency remains limited by the stability of carriers and the release kinetics of healing agents.In contrast,intrinsic self-healing polyurethane materials achieve self-healing through the reversibility of dynamic covalent and non-covalent bonds,which confer excellent self-healing capabilities while necessitating a precise balance between mechanical performance and self-healing efficiency.Moreover,their healing behavior is highly dependent on environmental conditions,potentially restricting their practical applications.Recent studies have demonstrated that the synergistic design of dynamic bonding networks can significantly enhance the mechanical properties,self-healing efficiency,and environmental adaptability.These developments offer new insights and theoretical foundations for designing high-performance self-healing polyurethane materials and may broaden their industrial applications.展开更多
This study identified castor oil and phosphate ester as effective retarders through setting time,tensile,and flexural tests,and determined their optimal dosages.The mechanism by which phosphate ester affects the setti...This study identified castor oil and phosphate ester as effective retarders through setting time,tensile,and flexural tests,and determined their optimal dosages.The mechanism by which phosphate ester affects the setting time of polyurethane was further investigated using molecular dynamics simulations.Fourier transform infrared spectroscopy was also employed to systematically study the physical and chemical interactions between phosphate esters and polyurethane materials.The results demonstrate that a 1%concentration of phosphate ester provides the most effective retarding effect with minimal impact on the strength of polyurethane.When phosphate ester is added to the B component of the two-component polyurethane system,its interaction energy with component A decreases,as do the diffusion coefficient and aggregation degree of component B on the surface of component A.This reduction in interaction slows the setting time.Additionally,the addition of phosphate ester to polyurethane leads to the disappearance or weakening of functional groups,indicating competitive interactions within the phosphate ester components that inhibit the reaction rate.展开更多
Shotcrete is one of the common solutions for shallow sliding.It works by forming a protective layer with high strength and cementing the loose soil particles on the slope surface to prevent shallow sliding.However,the...Shotcrete is one of the common solutions for shallow sliding.It works by forming a protective layer with high strength and cementing the loose soil particles on the slope surface to prevent shallow sliding.However,the solidification time of conventional cement paste is long when shotcrete is used to treat cohesionless soil landslide.The idea of reinforcing slope with polyurethane solidified soil(i.e.,mixture of polyurethane and sand)was proposed.Model tests and finite element analysis were carried out to study the effectiveness of the proposed new method on the emergency treatment of cohesionless soil landslide.Surcharge loading on the crest of the slope was applied step by step until landslide was triggered so as to test and compare the stability and bearing capacity of slope models with different conditions.The simulated slope displacements were relatively close to the measured results,and the simulated slope deformation characteristics were in good agreement with the observed phenomena,which verifies the accuracy of the numerical method.Under the condition of surcharge loading on the crest of the slope,the unreinforced slope slid when the surcharge loading exceeded 30 k Pa,which presented a failure mode of local instability and collapse at the shallow layer of slope top.The reinforced slope remained stable even when the surcharge loading reached 48 k Pa.The displacement of the reinforced slope was reduced by more than 95%.Overall,this study verifies the effectiveness of polyurethane in the emergency treatment of cohesionless soil landslide and should have broad application prospects in the field of geological disasters concerning the safety of people's live.展开更多
Doping perylene diimide(PDI)into a polymer matrix is a simple strategy to prepare near-infrared(NIR)reflective materials,but the mechanical properties and NIR reflectance properties are significantly compromised due t...Doping perylene diimide(PDI)into a polymer matrix is a simple strategy to prepare near-infrared(NIR)reflective materials,but the mechanical properties and NIR reflectance properties are significantly compromised due to macro-phase separation.In this study,a novel polymer(denoted as PU-PDI)with intrinsic NIR reflective proper⁃ties was synthesized by covalent incorporation of PDI units into polyurethane chains.Its photophysical characteris⁃tics,mechanical property and NIR reflectance property are investigated in detail.The results show that covalent in⁃corporation reduces the severe aggregation of PDI units,thereby endows PU-PDI with excellent mechanical property.The elongation at break of PU-PDI can reach more than 700%,and the breaking strength is 34.11 MPa.Moreover,compared to the blending system,PU-PDI possesses enhanced NIR reflection ability due to the better dispersion of PDI units.展开更多
Traditional hydrogels are inevitably damaged during practical applications,resulting in a gradual deterioration of their functional efficacy.A primary strategy to address this issue involves developing hydrogels with ...Traditional hydrogels are inevitably damaged during practical applications,resulting in a gradual deterioration of their functional efficacy.A primary strategy to address this issue involves developing hydrogels with inherent self-healing properties.In this study,we report the synthesis of self-healing polyacrylate hydrogels that integrate zwitterions,hydrophilic nano-silica and aluminum ions.Due to the synergistic effect of multiple hydrogen bonds,coordination bonds and electrostatic interactions,the tensile strength of the hydrogel is enhanced from 15.1 to 162.6 kPa.Moreover,the electrical resistance and tensile strength of the hydrogel can almost recover to its initial values after 20 min of healing at room temperature,exhibiting remarkable self-healing performance.Furthermore,the zwitterionic polyacrylate hydrogel serves as a wearable sensor with the capability of accurately response to the bending and stretching of human joints,exhibting a gauge factor of 1.87 under tensile strain ranging from 80% to 100%.Even after being freezed at-20℃ for 3 h,the zwitterionic polyacrylate hydrogel retains its exceptional writing performance.In conclusion,the hydrogels developed in this study demonstrate significant potential for wearable electronics applications.展开更多
基金The National Natural Science Foundation of China(No.52173077)the Liaoning Provincial Department of Education Series Project(No.LJKZ0187)+1 种基金Natural Science Foundation of Liaoning Province(No.2023-MS-239)Liaoning BaiQianWan Talents Program(No.2021921081)。
文摘In this study,a facile method was employed to synthesize strong,yet highly elastic polyurethane-urea(PUU)with typical characteristics and 94% optical transmittance.Graphene platelets(GNPs)were prepared and modified via a scalable and eco-friendly mechanochemical approach.The produced GNPs is at 1.6-nm thickness with high electrical conductivity of~950 S/m.The structure-property relations of PUU/GNP nanocomposites were comprehensively investigated through morphology and mechanical properties measurements.The strong interface and high-density hydrogen bonds between modified GNPs(M-GNPs)and PUU significantly enhanced the mechanical properties of the PUU nanocomposite.The PUU composite showed 66.7%and 36.2%increments in tensile and impact strengths,respectively,at 0.2 wt% M-GNPs.The reversible hydrogen bond between M-GNPs and PUU endowed the nanocomposite with self-healing properties achieving 97.8% healing efficiency of the strength after 5 h at 120℃.This study demonstrates the importance of surface modification and provides a simple yet robust approach for preparing high-performance and functional PUU/graphene composites.
基金financially supported by the National Natural Science Foundation of China(No.52503154)Shandong Provincial Natural Science Foundation(Nos.ZR2022MB034 and ZR2025QC512)。
文摘Azobenzene-based polymer actuators show great promise for photoactuation owing to their unique photoisomerization behavior and tailorable molecular programmability.However,conventional systems are limited by inadequate mechanical robustness,self-healing,and recyclability,hindering their practical implementation.Herein,we present a high-performance azobenzene-functionalized polyurethane(AzoPU)elastomer actuator designed via molecular engineering of photoactive azobenzene moieties and dynamic disulfide bonds.AzoPU exhibits exceptional mechanical properties with retained performance after multiple reshaping cycles,enabled by well-engineered hard-soft segments and synergistic stress dissipation from weak covalent bonds/hierarchical hydrogen bonds.It achieves over 93%self-healing efficiency at room temperature owing to the synergistic interplay of disulfide bonds in the polymer backbone and intermolecular hydrogen bonds.Furthermore,it demonstrates remarkable light-triggered actuation behavior,achieving a phototropic bending angle exceeding 180°toward the light source within 45 s.To showcase its practical potential,proof-of-concept photoactuated devices with flower-,hook-,and gripper-like and local-orientation processed strip-shaped structures were fabricated,which exhibited rapid and reversible light-triggered deformation.This study proposes a novel strategy for the development of intelligent polymeric materials that integrate light responsiveness,self-healing,and recyclability,thus holding great promise for applications in flexible electronics,smart actuators,and sustainable functional materials.
基金funded by the LPDP-RIIM,Research Grant No.18/IV/KS/06/2022 and 4830/IT3.L1/PT.01.03/P/B/2022,titled Pengembangan Produk Oriented Strand Board Unggul dari Kayu Ringan dan Cepat Tumbuh dalam Rangka Pengembangan Produk Biokomposit Prospektif.
文摘Recent advancements in developing tannin-based non-isocyanate polyurethane(NIPU)resins have unlocked new possibilities for sustainable and eco-friendly wood adhesives.Unlike conventional polyurethane,NIPUs eliminate hazardous isocyanates,offering safer alternatives for industrial applications.Tannin,a naturally occurring polyphenolic compound,plays a pivotal role in enhancing these resins’fire-resistance and super-hydrophobic properties.This review highlights key developments in synthesizing tannin-based NIPU,focusing on various polymerization techniques such as polyaddition,polycondensation,ring-opening polymerization,and rearrangement.These strategies contribute to improved mechanical strength,thermal stability,and resistance to water absorption.Recent studies demonstrate that tannin-based NIPU adhesives meet or exceed international internal bonding strength,elasticity,and durability standards.Their application in wood-based composites like oriented strand boards(OSB)has shown promising results,offering improved resistance to moisture and superior dimensional stability.Furthermore,the cross-linked polymer network,supported by chemical modifications like the introduction of fluoroalkyl groups,significantly enhances hydrophobicity and fire retardancy.Despite these advancements,challenges remain in terms of scalability,cost,and integration with existing manufacturing processes.Future research should focus on optimizing reaction conditions,improving raw material availability,and developing industrial-scale production methods.This review underscores the potential of tannin-based NIPU resins as a viable and sustainable alternative for various wood composite applications.
基金financially supported by the Hubei Key Laboratory of Pollutant Analysis&Reuse Technology(No.PA230102)。
文摘Polyurethane elastomers exhibit high dielectric constants owing to their polar groups,and can be used as energy storage capacitors.Energy storage depends not only on the dielectric constant but also on the dielectric loss.However,the relationship between chain structure and dielectric properties is not yet clear.Ketal-containing crosslinked polyurethane elastomers were prepared using cyclic ketal diol as a chain extender.The effect of the soft segment length on the dielectric properties and energy storage was investigated.The cause of the change in the dipolar polarization with the soft segment length was analyzed.As the soft segment length increased,the hard-soft hydrogen bonding decreased,whereas the hard-hard hydrogen bonding increased.Under the action of an electric field,the polar bonds in the ketal-containing polyurethane elastomer overcome the hydrogen bonding between hard-soft segments to produce polarization;meanwhile,they also experience crankshaft motions to generate polarization.The former has a relatively high relaxation activation energy of approximately 10-20 k J·mol^(-1),resulting in a large dielectric loss.The latter has a relatively low relaxation activation energy,approximately 0.7-1.7 kJ·mol^(-1),leading to low dielectric loss.As a result,the dielectric constant showed a decreasing trend,and the dielectric loss gradually decreased.This study provides a theoretical foundation for improving the dielectric properties of polyurethane elastomers.
基金supported by the National Natural Science Foundation of China(Nos.51603005,52403186 and 52573150)Fujian Provincial Natural Science Foundation of China(No.2024J011447)+1 种基金Natural Science Foundation of Xiamen,China(No.3502Z20227305)the Postdoctoral Fellowship Program of CPSF(No.GZC20240095)。
文摘Near-infrared(NIR)light-responsive shape memory polymers(SMPs)show great promise for biomedical applications,but conventional photothermal agents suffer from high cost,complex preparation,or poor biocompatibility,while lignin-based alternatives exhibit insufficient photothermal conversion efficiency.Herein,we developed a novel strategy to enhance photothermal performance of lignin through sequential demethylation modification and Fe^(3+)complexation for constructing NIR light responsive SMPs.Dealkaline lignin(DL)was first demethylated using iodocyclohexane to produce demethylated lignin(DDL)with increased catechol content,which was then incorporated into polycaprolactone-based polyurethane synthesis followed by Fe^(3+)complexation.Results showed that DDL-Fe^(3+)complexes have significantly enhanced photothermal conversion performance,and the resulting PU-DDL+Fe^(3+)polyurethane with 0.5 wt%DDL content demonstrated a temperature increases of 39.8℃under 0.33 W·cm-2808 nm NIR irradiation.This excellent photothermal performance enables the shape-fixed PU-DDL+Fe^(3+)polyurethane to rapidly recover to its initial shape under NIR light irradiation.Additionally,PU-DDL+Fe^(3+)polyurethane exhibits good mechanical properties and biocompatibility,demonstrating significant biomedical application potential.
文摘The development of intrinsically conductive piezoresistive sensors with high strain tolerance has garnered significant interest.While elastomeric polymers exhibit excellent strain capabilities,their utility in sensing applications has been limited by inherent challenges such as high electrical resistivity,poor aging resistance,and interfacial incompatibility.To address these limitations,hydroxyl-terminated polybutadiene(HTPB)-based polyurethane was chemically modified with acetylferrocene-polyaniline conductive moieties to enhance charge transport properties.Remarkably,this covalent functionalization endowed the resulting ferrocene-polyaniline hybrid polyurethane(FPHP)with a conductivity of2.33 n A at 1 V bias while preserving piezoresistive functionality.The FPHP demonstrated exceptional mechanical-electrical performance,achieving 254% elongation at break with strain-dependent gauge factors of 7.28(0%-12.5% strain,R^(2)=0.9504)and 19.66(12.5%-35.0% strain,R^(2)=0.9929).Further characterization revealed a rapid 0.60 s response time and stability over 3500 strain-release cycles at compression strain,underscoring its durability under repetitive loading.The FPHP sensor was capable of monitoring various human movements and recognizing writing signals.These advances establish a materials design paradigm for fabricating flexible sensors that synergistically integrate high deformability,tunable sensitivity,and robust operational stability,positioning FPHP as a promising candidate for next-generation wearable electronics and soft robotics.
基金supported by the Natural Science Foundation of Shandong Province(ZR2022QE042)China Postdoctoral Science Foundation(2023M741856)the National Natural Science Foundation of China(52172093).
文摘Pyrolysis technology has emerged as a promising method for converting waste polyurethane(WPU)from waste refrigerators into high-value chemicals.In this study,the copper(Cu)-assisted pyrolysis strategy was employed to enhance the thermal degradation efficiency and product quality of WPU.Kinetic analysis revealed that the activation energy(E_(a)) of the Cu-assisted pyrolysis was 136.64 kJ·mol^(−1) and Cu-assisted pyrolysis was controlled by the combined processes of diffusion,nucleation and phase boundary reactions.Comprehensive product analysis,including gas chromatography–mass spectrometry and thermogravimetric Fourier transform infrared spectroscopy–mass spectrometry suggested that Cu promoted the cleavage of urethane bonds and accelerated the decarboxylation of isocyanates,increasing the yields of aniline and ethanol at lower temperatures.Meanwhile,Cu effectively suppressed the formation of halogenated and heterocyclic compounds by promoting the cleavage of C–X(X=Cl,F)bonds through electron transfer interactions.Thus,the E_(a) is decreased and the halogenated compounds is reduced.This work provides the theoretical basis for converting waste to high-valued products through co-pyrolysis techniques.
基金supported by the National Natural Science Foundation of China(U23A20605,22075053)Anhui Provincial Natural Science Foundation(No.2108085ME178)Student Research Training Program(No.S202410360232).
文摘In view of the problems such as the low utilization efficiency of copper tailings solid waste,which leads to severe environmental pollution,and the easy combustibility of rigid polyurethane foam(RPUF)along with the generation of a large amount of toxic smoke during combustion,copper tailings were combined with melamine polyphosphate to prepare RPUF composites.The flame-retardant properties were investigated,and the structure–property relationship was clarified.It was found that when 16.7 g of copper tailings and 33.3 g of melamine polyphosphate were added,the limiting oxygen index increased to 23.0 vol.%,and the vertical burning rating(UL-94)reached V-0.The peak heat release rate was reduced by 27.79%compared to pure RPUF,and the fire growth index decreased to 4.54 kW/(m^(2)s),representing a 75.42%reduction.The char residue rate at 750℃ increased from 17.6% to 28.51%.Moreover,the addition of copper tailings and melamine polyphosphate effectively promoted the charring of RPUF,forming a dense char layer with good fire resistance performance.
基金financially supported by the National Natural Science Foundation of China(No.52303063)Hubei Provincial Department of Education Guided Scientific Research Project(No.B2024056)。
文摘Airless tires are essential for enhancing the safety,reliability,and convenience of maintenance of electric bicycles.Polyurethane(PU)is considered a promising candidate for such applications owing to its versatile properties.However,their use is limited by insufficient heat resistance and excessive dynamic heat generation under cyclic loading.In this study,star-shaped trifunctional polypropylene glycerol(PPG3)was incorporated into conventional poly(tetramethylene glycol)(PTMG)and 4,4'-methylenediphenyl diisocyanate(MDI)-based systems to construct microporous star-shaped casting polyurethanes(SCPU),with water serving as a green foaming agent.Unlike conventional small-molecule trifunctional crosslinkers that create junctions within hard segment domains,PPG3 introduces long flexible arms between the hard segments,anchoring the crosslinking points at its molecular core.The large steric hindrance of PPG3 effectively suppresses soft segment crystallization and lowers the degree of microphase separation,whereas the crosslinked network restricts chain mobility,thereby reducing dynamic heat generation.These structural features also enhance the heat resistance,yielding a softening temperature of 183℃,which is 30.9%higher than that of polyurethane without PPG3.When applied to airless tires by casting SCPU into rubber treads,the fabricated hybrid airless tires achieved a rolling distance of over 3000 km under a load of 65 kg at 25km/h without structural failure,satisfying practical performance requirements.This strategy offers a simple,solvent-free,and environmentally friendly process,underscoring the potential of SCPU for scalable production of high-performance airless tires.
基金supported by the Russian state-funded project for ICBFM SB RAS(grant number 125012300656-5)。
文摘Background:The development of materials for cardiovascular surgery that would improve the effectiveness of surgical interventions remains an important task.Surgical intervention during the implantation of vascular prostheses and stents,and the body’s reaction to artificial materials,could lead to chronic inflammation,a local increase in the concentration of proinflammatory factors,and stimulation of unwanted tissue growth.The introduction of nonsteroidal anti-inflammatory drugs into implantable devices could be used to obtain vascular implants that do not induce inflammation and do not induce neointimal tissue outgrowth.Methods:The scaffolds were made by electrospinning from mixtures of polyurethane(PU)with diclofenac(DF).The kinetics of DF release from the scaffolds composed of 3%PU/10%HSA/3%DMSO/DF and 3%PU/DF were studied.The biocompatibility and anti-inflammatory effects of the obtained scaffolds on human gingival fibroblasts and umbilical vein endothelial cells were studied.Results:Both types of scaffolds are characterized by fast DF release.The viability of cells cultured on scaffolds is 2 times worse than that of cells cultured on plastic.The level of the proinflammatory cytokine IL-6 in the culture medium of cells cultured on DF-containing scaffolds was lower than that of cells cultured on scaffolds without DF.Conclusion:The introduction of DF into scaffolds minimizes the inflammation caused by cell reactions to an artificial material.
基金supported by the National Natural Science Foundation of China(No.51905543)。
文摘This study aimed to systematically regulate the performance of 4D printing composites by investigating the synergistic effects of dicumyl peroxide(DCP)and maleic anhydride-grafted polyethylene(MAH-g-PE)on a poly(lactic acid)/thermoplastic polyurethane(PLA/TPU)matrix.Specifically,using a 70 wt%/30 wt%PLA/TPU matrix and an L_(9)(3^(2))orthogonal design,composites were evaluated via morphology,shape memory,mechanical tests,and multi-criteria analysis.Moderate DCP enhanced crosslinking,improving storage modulus and thermal stability,while excessive DCP caused brittleness.Furthermore,MAH-g-PE effectively improved interfacial compatibility,and its synergy with DCP was dosage-dependent.Consequently,Sample 5 achieved optimal performance,exhibiting uniform fracture morphology,a shape fixation rate of98.8%with the fastest recovery,and balanced strength-ductility.Multi-criteria analysis identified elongation at break and recovery time as the top contributing factors,with consistent rankings validated by Spearman analysis(ρ=0.833,p<0.01).In summary,adjusting DCP and MAH-g-PE contents effectively modulates the crosslinking structure and interfacial properties of PLA/TPU composites,providing a viable strategy for developing high-performance,tunable 4D printing materials.
文摘A polyacrylate/polyurethane (P(A)/P(U)) composite coating has been prepared by crosslinking an acetoacetylated polyacrylate with a vinylic group terminated polyurethane at room temperature. A model Michael reaction between ethyl acetoacetate (EAA) and methyl acrylate (MA) was designed to study the crosslinking mechanism. It was found that the two active hydrogen atoms in acetoacetyl group can both add to vinylic groups and the yield of mono-and bis-adducts are much affected by the molar ratio of acetoacetyl to vinylic groups. Higher crosslinking degree and better properties could be obtained with decreasing the molar ratio of the two active groups from 1/1 to 0.6/1 in the composite coatings.
基金financially supported by the National Key Research and Development Program of China(2022YFE0138900)the National Natural Science Foundation of China(21972017)the“Scientific and Technical Innovation Action Plan”Basic Research Field of Shanghai Science and Technology Committee(19JC1410500).
文摘Developing advanced ion-conductive networks is crucial for anion exchange membranes(AEMs).A flexible molecular structure facilitates the formation of ion clusters,resulting in enhanced ionic conductivity.Polyacrylates,known for their outstanding flexibility and chemical stability,hold significant potential as polymer electrolyte membranes.In this work,we innovatively constructed a series of polyacrylate-based AEMs decorated with pendant zwitterions(designated as PSBPA-X,BSBPA-X,where X=20,30,40).Specifically,the spacer length between the zwitterions is strategically optimized to enhance the ionic conductivity.Atomic force microscopy reveals that a longer spacer length between the zwitterions promotes the microphase separation and the formation of advanced water channels,which facilitates the OH^(-)transport in the BSBPA-40 membrane.Moreover,the stronger electrostatic potential and lower interaction energy between the BSBPA-40 and OH^(-)further contribute to efficient OH^(-)hopping transmission.Consequently,the BSBPA-40 membrane demonstrates the highest OH^(-)conductivity,achieving 102.1 mS cm^(-1)at 80℃ and 90% relative humidity,significantly surpassing that of the PSBPA-40 membrane(75.2 mS cm^(-1)).Additionally,the BSBPA-40 membrane exhibits remarkable flexibility with an improved breaking elongation of 480.5%due to the ionic cross-linking between the zwitterions.Notably,the BSBPA-40 membrane-based zinc-air battery achieves an outstanding power density of 156.7 mW cm^(-2)at room temperature,while its water electrolysis performance reaches 2.1 A cm^(-2)at 2.0 V.These results indicate that the developed membranes hold great promise for applications in sustainable and clean energy technologies.
基金financially supported by the National Key Research and Development Program of China(Grant Nos.2023YFB2604005)the National Key Research and Development 451 Program of China(Grant No.2021YFC3100803)the Yangtze River Water Science Research Joint Fund Key Project of National Natural Science Foundation of China(Grant No.U2340231).
文摘Polyurethane foam,when used as a compressible layer in deep soft rock tunnels,offers a feasible solution to reduce the support pressure on the secondary lining.The foam spraying method using sprayed polyurethane material is convenient for engineering applications;however,the compressive behaviour and feasibility of sprayed polyurethane material as a compressible layer remain unclear.To address this gap,this study conducts uniaxial compression tests and scanning electron microscope(SEM)tests to investigate the compressive behaviour of the rigid foams fabricated from a self-developed polyurethane spray material.A peridynamics model for the composite lining with a polyurethane compressible layer is then established.After validating the proposed method by comparison with two tests,a parametric study is carried out to investigate the damage evolution of the composite lining with a polyurethane compressible layer under various combinations of large deformations and compressible layer parameters.The results indicate that the polyurethane compressible layer effectively reduces the radial deformation and damage index of the secondary lining while increasing the damage susceptibility of the primary lining.The thickness of the polyurethane compressible layer significantly influences the prevention effect of large deformation-induced damage to the secondary lining within the density range of 50e100 kg/m^(3).In accordance with the experimental and simulation results,a simple,yet reasonable and convenient approach for determining the key parameters of the polyurethane compressible layer is proposed,along with a classification scheme for the parameters of the polyurethane compressible layer.
基金supported by the Basic Science Research Program through the National Research Foundation of Korea(NRF)funded by the Ministry of Science and ICT(RS-2024-00451587)supported by Post-plastic Specialized Graduate Program through the Korea Environmental Industry&Technology Institute(KEITI)funded by the Ministry of Environment(MOE).
文摘Bio-polyol is considered as a core material to synthesize eco-friendly polyurethane products.However,one of the popular bio-polyols,polytrimethylene ether glycol(PO3G),is reluctant to crystallize and therefore exhibits a cold crystallization behavior.This abnormal behavior causes unstable mechanical properties at low-temperature and limits its applications in shape memory devices where crystallization is an essential mechanism.To analyze the unusual phenomenon,we compared different ether polyols focusing on symmetry characteristics and the evenodd effect of carbon backbones.It is found that PO3G has a slow crystallization rate because its ether linkages require specific chain arrangement for attractive interactions.Consequently,a thermal learning mechanism is developed to restore the normal crystallization behavior of elastomers synthesized from the bio-polyol.Repetitive heating and cooling cycles with high-temperature annealing induce urethane exchange reaction and reconstruct the chain orientations for fast crystallization.Results suggest the degree of crystallizations in polyurethane elastomer can be precisely controlled by introducing repetitive thermal treatments to enhance the potential applications of bio-polyols in polymer industries.
基金sponsored by the National Key Research and Devel-opment Program of China(2023YFD1800105)Guangdong Province Science&Technology Program(2024B1515040004)Guangzhou Sci-ence and Technology Plan Project(2024A04J6354).
文摘As a significant branch of smart materials,self-healing polyurethane materials mimic the biological damage repair mechanisms and have been widely applied in flexible electronics,functional coatings,biomedicine,and other fields.This review systematically summarizes the design principles and recent advancements in both extrinsic and intrinsic self-healing polyurethane materials,highlighting their respective self-healing mechanisms and characteristics.For extrinsic system,damage repair is primarily achieved through microcapsules,hollow fibers,nanoparticles,and microvascular networks.However,their healing efficiency remains limited by the stability of carriers and the release kinetics of healing agents.In contrast,intrinsic self-healing polyurethane materials achieve self-healing through the reversibility of dynamic covalent and non-covalent bonds,which confer excellent self-healing capabilities while necessitating a precise balance between mechanical performance and self-healing efficiency.Moreover,their healing behavior is highly dependent on environmental conditions,potentially restricting their practical applications.Recent studies have demonstrated that the synergistic design of dynamic bonding networks can significantly enhance the mechanical properties,self-healing efficiency,and environmental adaptability.These developments offer new insights and theoretical foundations for designing high-performance self-healing polyurethane materials and may broaden their industrial applications.
基金Funded by the National Natural Science Foundation of China(No.52370128)the Fundamental Research Funds for the Central Universities(No.2572022AW54)。
文摘This study identified castor oil and phosphate ester as effective retarders through setting time,tensile,and flexural tests,and determined their optimal dosages.The mechanism by which phosphate ester affects the setting time of polyurethane was further investigated using molecular dynamics simulations.Fourier transform infrared spectroscopy was also employed to systematically study the physical and chemical interactions between phosphate esters and polyurethane materials.The results demonstrate that a 1%concentration of phosphate ester provides the most effective retarding effect with minimal impact on the strength of polyurethane.When phosphate ester is added to the B component of the two-component polyurethane system,its interaction energy with component A decreases,as do the diffusion coefficient and aggregation degree of component B on the surface of component A.This reduction in interaction slows the setting time.Additionally,the addition of phosphate ester to polyurethane leads to the disappearance or weakening of functional groups,indicating competitive interactions within the phosphate ester components that inhibit the reaction rate.
基金the financial support from the Fujian Science Foundation for Outstanding Youth(2023J06039)the National Natural Science Foundation of China(Grant No.41977259,U2005205,41972268)the Independent Research Project of Technology Innovation Center for Monitoring and Restoration Engineering of Ecological Fragile Zone in Southeast China(KY-090000-04-2022-019)。
文摘Shotcrete is one of the common solutions for shallow sliding.It works by forming a protective layer with high strength and cementing the loose soil particles on the slope surface to prevent shallow sliding.However,the solidification time of conventional cement paste is long when shotcrete is used to treat cohesionless soil landslide.The idea of reinforcing slope with polyurethane solidified soil(i.e.,mixture of polyurethane and sand)was proposed.Model tests and finite element analysis were carried out to study the effectiveness of the proposed new method on the emergency treatment of cohesionless soil landslide.Surcharge loading on the crest of the slope was applied step by step until landslide was triggered so as to test and compare the stability and bearing capacity of slope models with different conditions.The simulated slope displacements were relatively close to the measured results,and the simulated slope deformation characteristics were in good agreement with the observed phenomena,which verifies the accuracy of the numerical method.Under the condition of surcharge loading on the crest of the slope,the unreinforced slope slid when the surcharge loading exceeded 30 k Pa,which presented a failure mode of local instability and collapse at the shallow layer of slope top.The reinforced slope remained stable even when the surcharge loading reached 48 k Pa.The displacement of the reinforced slope was reduced by more than 95%.Overall,this study verifies the effectiveness of polyurethane in the emergency treatment of cohesionless soil landslide and should have broad application prospects in the field of geological disasters concerning the safety of people's live.
文摘Doping perylene diimide(PDI)into a polymer matrix is a simple strategy to prepare near-infrared(NIR)reflective materials,but the mechanical properties and NIR reflectance properties are significantly compromised due to macro-phase separation.In this study,a novel polymer(denoted as PU-PDI)with intrinsic NIR reflective proper⁃ties was synthesized by covalent incorporation of PDI units into polyurethane chains.Its photophysical characteris⁃tics,mechanical property and NIR reflectance property are investigated in detail.The results show that covalent in⁃corporation reduces the severe aggregation of PDI units,thereby endows PU-PDI with excellent mechanical property.The elongation at break of PU-PDI can reach more than 700%,and the breaking strength is 34.11 MPa.Moreover,compared to the blending system,PU-PDI possesses enhanced NIR reflection ability due to the better dispersion of PDI units.
基金financially supported by the National Key Research and Development Program of China(2022YFE0138900)the National Natural Science Foundation of China(21972017)+1 种基金the Fundamental Research Funds for the Central Universities of Ministry of Education of China(D5000240188)the"Scientific and Technical Innovation Action Plan"Basic Research Field of Shanghai Science and Technology Committee(19JC1410500)。
文摘Traditional hydrogels are inevitably damaged during practical applications,resulting in a gradual deterioration of their functional efficacy.A primary strategy to address this issue involves developing hydrogels with inherent self-healing properties.In this study,we report the synthesis of self-healing polyacrylate hydrogels that integrate zwitterions,hydrophilic nano-silica and aluminum ions.Due to the synergistic effect of multiple hydrogen bonds,coordination bonds and electrostatic interactions,the tensile strength of the hydrogel is enhanced from 15.1 to 162.6 kPa.Moreover,the electrical resistance and tensile strength of the hydrogel can almost recover to its initial values after 20 min of healing at room temperature,exhibiting remarkable self-healing performance.Furthermore,the zwitterionic polyacrylate hydrogel serves as a wearable sensor with the capability of accurately response to the bending and stretching of human joints,exhibting a gauge factor of 1.87 under tensile strain ranging from 80% to 100%.Even after being freezed at-20℃ for 3 h,the zwitterionic polyacrylate hydrogel retains its exceptional writing performance.In conclusion,the hydrogels developed in this study demonstrate significant potential for wearable electronics applications.
