Epoxy resin based Unsaturated poly(ester-amide) resins (UPEAs) can be prepared by many methods but here these were prepared by reported method [1]. These UPEAs were then treated with acrylotl chloride to afford acryla...Epoxy resin based Unsaturated poly(ester-amide) resins (UPEAs) can be prepared by many methods but here these were prepared by reported method [1]. These UPEAs were then treated with acrylotl chloride to afford acrylated UPEAs resin (i.e. AUPEAs). Interacting blends of equal proportional AUPEAs and vinyl ester epoxy (VE) resin were prepared. APEAs and AUPEAs were characterized by elemental analysis, molecular weight determined by vapour pressure osmometer and by IR spectral study and by thermogravimetry. The curing of interacting blends was monitored on differential scanning calorimeter (DSC). Based on DSC data in situ glass reinforced composites of the resultant blends have been prepared and characterized for mechanical, electrical and chemical properties. Unreinforced blends were characterized by thermogravimetry (TGA).展开更多
A novel phosphorous-containing acrylated epoxidized soybean oil-based(P-AESO)resin was developed via the ring-opening reaction of epoxidized soybean oil(ESO)with diphenylphosphinic chloride(DPPC),followed by acrylatio...A novel phosphorous-containing acrylated epoxidized soybean oil-based(P-AESO)resin was developed via the ring-opening reaction of epoxidized soybean oil(ESO)with diphenylphosphinic chloride(DPPC),followed by acrylation of the resulting groups.The chemical structure was characterized by Fourier transform infrared spectroscopy(FT-IR),and ^(1)H nuclear magnetic resonance(^(1)H NMR).Subsequently,the viscosity and volumetric shrinkage of the obtained P-AESO resins were studied.Then the oligomer was formulated into UV-curable coatings,and the mechanical,thermal,and coating properties of the resulting UV-cured bioresins were studied by tensile testing,dynamic mechanical thermal analysis(DMA),thermogravimetric analysis(TGA)coupled with FT-IR spectroscopy(TGA-FT-IR),hardness,adhesion,pencil hardness and chemical resistance.Furthermore,the UV-curing behavior of the P-AESO resin was determined by real-time realtime infrared(RT-IR).Meanwhile,compared with coating from acrylated epoxidized soybean oil(AESO),the P-AESO system coatings showed better volumetric shrinkage,excellent adhesion,and enhanced thermal and glass transition temperature(Tg)while maintaining reasonably final C=C conversions and cross-link density.For instance,the obtained P-AESO/trimethylolpropanetriacrylate(TMPTA)20 material possessed a volumetric shrinkage of 4.1%,Tg of 115.6℃,char yield of 9.47%,and final C=C conversions of 81.4%respectively,which exhibited superior values than that of the AESO/TMPTA20 material.The improvement of the P-AESO coating performances could contribute to the architectures that combined the structural features of phosphorous-containing rigid benzene.The developed P-AESO resin is promising for applications in the UV-curable coatings.展开更多
In ultraviolet cured-in-place-pipe(UV-CIPP)pipeline rehabilitation,resin performance critically determines repair effectiveness.Current UV-curable resins exhibit high volatile organic compound(VOC)emissions and inadeq...In ultraviolet cured-in-place-pipe(UV-CIPP)pipeline rehabilitation,resin performance critically determines repair effectiveness.Current UV-curable resins exhibit high volatile organic compound(VOC)emissions and inadequate post-cure toughness,which compromise fatigue resistance during service.To address these issues,we synthesized hydroxyl-terminated polyurethane acrylate prepolymers using diphenylmethane diisocyanate(MDI),polypropylene glycol(PPG),and hydroxyethyl methacrylate(HEMA).Fourier transform infrared spectroscopy(FTIR)confirmed successful prepolymer synthesis.We developed UV-curable resins by incorporating various crosslinking monomers and optimized the formulations through mechanical property analysis.Testing revealed that the polyurethane-acrylic UV-cured resin system combines polyurethane's mechanical excellence with acrylics'high UV-curing activity.The PPG200/MDI/HEMA formulation achieved superior performance,with a tensile strength of 55.31 MPa,an impact toughness of 22.7 kJ/m^(2),and a heat deflection temperature(HDT)of 132℃.The optimized system eliminates volatile components while maintaining high reactivity,addressing critical limitations in trenchless pipeline rehabilitation.The improved mechanical properties meet the operational demands of underground pipes,suggesting practical applicability in trenchless pipeline repair.展开更多
Synergy strategy of photocatalysts and polymer resins are promising technology for marine antifouling.However,it is still a main challenge to obtain a green,safe,and efficient antifouling coatings.Herein,carbon(graphe...Synergy strategy of photocatalysts and polymer resins are promising technology for marine antifouling.However,it is still a main challenge to obtain a green,safe,and efficient antifouling coatings.Herein,carbon(graphene or CNT)modified Ti O_(2)photocatalyst was synthesized via hydrothermal and annealing process and has successfully applied in acrylate fluoroboron polymer(ABFP)composite coating.Morphology and chemical composition were detailed characterized.The graphene or CNT acted as a bridge with supplemental spatial structures(petal gaps,entanglement)and new functional groups(C-O,C-Ti-O,etc.)on Ti O_(2)particle.Carbon nanotube(CNT)modified TiO_(2)-ABFP coatings(BTCP)achieved excellent antibacterial and anti-diatom adhesion rate of 89.3%-96.70%and 99.00%-99.50%,which was 1.84-4.94-fold more than that of the single ABFP.CNT or graphene served as electronic bridges was considered as the crucial mechanism,which significantly improved the light absorption range and capacity,conductivity,and photoelectric response of Ti O_(2),and further accelerated the generation and transfer of free radicals to the surface of BTCP or FTGP.Moreover,the improvement of catalyst activity synergizes with the smooth surface,hydrophilicity,and slow hydrolysis of composite coatings,achieved long-term and efficient antifouling performance.This work provides a new insight into the modification of Ti O_(2)and antifouling mechanism of polymer coating.展开更多
A novel composite material,Poly(IL-AA)@MIL-101(Cr),combining metal-organic framework,polymeric ionic liquid and acrylic acid,was synthesized for the selective and efficient adsorption of rare earths europium(Ⅲ)(Eu3+)...A novel composite material,Poly(IL-AA)@MIL-101(Cr),combining metal-organic framework,polymeric ionic liquid and acrylic acid,was synthesized for the selective and efficient adsorption of rare earths europium(Ⅲ)(Eu3+).Characterization of the materials was carried out using techniques such as X-ray diffraction(XRD),Fourier transform infrared(FTIR),scanning electron microscopy-energy dispersive X-ray spectroscopy(SEM-EDS),thermogravimetric analysis(TGA)and Brunauer-Emmett-Teller(BET).The results demonstrate successful incorporation of the polymeric ionic liquid onto the material surface while preserving the crystal structure and mo rphology of MIL-101(Cr).Adsorption experiments were conducted to explore parameters including equilibrium pH,initial Eu3+concentration,and duration,with comprehensive analyses of adsorption kinetics,isotherms,and mechanisms.Findings reveal that Poly(IL1-AA)@MIL-101(Cr),Poly(IL3-AA)@MIL-101(Cr),and Poly(IL5-AA)@MIL-101(Cr)achieve adsorption equilibrium for Eu3+at approximately 9 h with an equilibrium pH of 6.2.The adso rption of Eu^(3+)predominantly follows a pseudo-second-order kinetic model and Langmuir isotherm adsorption model.Moreover,the prepared composite material exhibits superior adsorption selectivity for Eu^(3+)over other metal ions in the mixture(K^(+),Mg^(2+),Ni^(2+),Co^(2+),Zn^(2+),La^(3+),and Nd^(3+)).Even after five adsorption-desorption cycles,the composite material maintains satis factory adsorption performance.展开更多
Modified activated carbons(AS)were fabricated through the oxidation effect of ammonium persulfate and applied to the dynamic adsorption of different acrylate gas.The pore structures,surface chemical properties and sur...Modified activated carbons(AS)were fabricated through the oxidation effect of ammonium persulfate and applied to the dynamic adsorption of different acrylate gas.The pore structures,surface chemical properties and surface morphology of AS were respectively characterized by N2 adsorption,Boehm titration,X-ray Photoelectron Spectroscopy(XPS)and scanning electron microscopy(SEM)techniques.After modification,the specific surface area increased from 954 to 1154 m^(2)·g^(-1).The contents of oxygen-containing functional groups on the AS surface increase obviously and have a great effect on the adsorption behavior of acrylate gases.According to the results of dynamic adsorption,the adsorption capacities of acrylates are as the following order:methyl acrylate(461.9 mg·g^(-1))>methyl methacrylate(436.9 mg·g^(-1))>butyl acrylate(381.8 mg·g^(-1)),which is attributed to the size adaptability of AS pores and acrylates.The adsorption behavior of AS for acrylate gases conforms to the Bangham model and the Temkin model.展开更多
Flexible wearable electronic devices based on hydrogels have immense potential in a wide range of applications.However,many existing strain sensors suffer from significant limitations including poor mechanical propert...Flexible wearable electronic devices based on hydrogels have immense potential in a wide range of applications.However,many existing strain sensors suffer from significant limitations including poor mechanical properties,low adhesion,and insufficient conductivity.To address these challenges,this study successfully developed an organic-inorganic double-network conductive hydrogel using acrylic-modified bentonite (AABT) as a key component.The incorporation of AABT significantly enhanced the mechanical properties of the ATHG@LiCl hydrogel,achieving an impressive stretchability of 4000% and tensile strength of 250 kPa.Moreover,it improved the electrical conductivity of the hydrogel to a maximum of 1.53 mS/cm.The catechol structure of tannic acid (TA) further augmented the adhesive properties of the ATHG@LiCl hydrogel toward various substrates such as copper,iron,glass,plastic,wood,and pigskin.The addition of lithium chloride (LiCl) and dimethyl sulfoxide(DMSO) endowed the hydrogel with exceptional freezing resistance and flexibility,even at low temperatures of-20℃.Remarkably,the hydrogel maintained a conductivity of 0.53 mS/cm under these conditions,surpassing the performance of many other reported hydrogels.Furthermore,the ATHG@LiCl hydrogel demonstrated outstanding characteristics,such as high sensitivity (gauge factor GF=4.50),excellent transparency (90%),and reliable strain-sensing capabilities,indicating that the ATHG@LiCl hydrogel is a highly promising candidate for flexible wearable soft materials,offering significant advancements in both functionality and performance.展开更多
Vanadium phosphorus oxide(VPO)catalyst is a promising candidate for the condensation reaction of formaldehyde(FA)and acetic acid(HAc)to produce acrylic acid(AA).However,the complexity of the active phases and their dy...Vanadium phosphorus oxide(VPO)catalyst is a promising candidate for the condensation reaction of formaldehyde(FA)and acetic acid(HAc)to produce acrylic acid(AA).However,the complexity of the active phases and their dynamic interconversion under redox conditions has led to controversies regarding the actual active phase in this reaction.To address this,this study systematically investigates the phase transition and underlying mechanism of VPO catalysts under reaction conditions.X-ray diffraction(XRD)patterns,Raman spectra,transmission electron microscopy images and X-ray photoelectron spectroscopy collectively demonstrated that the V^(4+)phase(VO)_(2)P_(2)O_(7)retained the bulk phase structure throughout the reaction,with only minor surface phase transition observed.In contrast,the V^(5+)phase underwent reduction to other phases in both bulk and surface regions.Specifically,theδ-VOPO_(4)phase rapidly transformed into theαII-VOPO_(4)phase,which could reversibly convert into the R1-VOHPO_(4)phase(V^(4+)).Controlled variable experiments,H_(2)-temperature programmed reduction and in-situ XRD experiments in a hydrogen atmosphere further demonstrated that these phase transitions were primarily attributed to the loss of lattice oxygen.The presence of V^(4+)phase in VPO catalysts enhanced the selectivity of acrylic acid,while the existence of V^(5+)phase promoted the activation of acetic acid.This work elucidates the redox-driven phase evolution of VPO catalysts and offers valuable insights for designing efficient catalysts for FA-HAc cross-condensation by balancing phase stability and activity.展开更多
Toray Industries,Inc.announced that from this April,it will im-plement the mass balance approach in manufacturing its TORAY-LON TMacrylic staple fiber.This method attributes properties fromboth biomass and plastic was...Toray Industries,Inc.announced that from this April,it will im-plement the mass balance approach in manufacturing its TORAY-LON TMacrylic staple fiber.This method attributes properties fromboth biomass and plastic waste,contributing to sustainabillty.Thecompany has already secured ISCC(nternational Sustainability&Carbon Certification)PLUScertification for this initiative.展开更多
Power cables are important pieces of equipment for energy transmission,but achieving a good balance between flame retardancy and mechanical properties of cable sheaths remains a challenge.In this work,a novel intumesc...Power cables are important pieces of equipment for energy transmission,but achieving a good balance between flame retardancy and mechanical properties of cable sheaths remains a challenge.In this work,a novel intumescent flame retardant(IFR)system containing silicone-containing macromolecular charring agent(Si-MCA)and ammonium polyphosphate(APP)was designed to synergistically improve the flame retardancy and mechanical properties of ethylene-butyl acrylate copolymer(EBA)composites.The optimal mass ratio of APP/Si-MCA was 3/1 in EBA composites(EBA/APP-Si-31),corresponding to the best flame retardancy with 31.2% of limited oxygen index(LOI),V-0 rating in UL-94 vertical burning test,and 76.4%reduction on the peak of heat release rate(PHRR)in cone calorimeter test.The enhancement mechanism was attributed to the synergistic effect of APP/Si-MCA during combustion,including the radical-trapping effect,the dilution effect of non-flammable gases,and the barrier effect of the intumescent char layer.Meanwhile,the tensile results indicated that EBA/APP-Si-31 also exhibited good mechanical properties with the addition of maleic anhydride-grafted polyethylene(PE-g-MA)as the compatibilizer.Thus,the APP/Si-MCA combination is an effective IFRs system for preparing high-performance EBA composites,and it will promote their applications as cable sheath materials.展开更多
In this study,an amine-reactive poly(pentafluorophenyl acrylate)(PPFPA)platform was developed for advanced surface engineering of next-generation sequencing(NGS)chips.Through post-polymerization modification,PPFPA was...In this study,an amine-reactive poly(pentafluorophenyl acrylate)(PPFPA)platform was developed for advanced surface engineering of next-generation sequencing(NGS)chips.Through post-polymerization modification,PPFPA was functionalized with dual moieties:azide groups for covalent immobilization of DBCO-modified DNA primers via click chemistry and tunable hydrophilic side chains to optimize biocompatibility and surface properties.Systematic screening revealed that hydrophobic azide carriers combined with neutral hydroxyl groups maximized the DNA immobilization efficacy,approaching the performance of commercial polyacrylamide-based polymers.The negatively charged carboxyl groups severely impede DNA primer attachment.Higher molecular weight derivatives further enhance the efficacy of DNA immobilization.In NGS validation,optimized surface modification polymers achieved robust surface density of clustered DNA and high sequencing accuracy,surpassing quality benchmarks and comparable to those of conventional analogs.This platform demonstrates significant potential for tailoring high-sensitivity surfaces for genomic applications,advancing clinical diagnostics,and personalized medicine.展开更多
Different-sized hollow SiO2 spheres of 249–1348 nm in diameter were successfully prepared by using Na2SiO3 as the precursor and using polystyrene and polystyrene-methyl acrylic acid latexes as the templates. The diam...Different-sized hollow SiO2 spheres of 249–1348 nm in diameter were successfully prepared by using Na2SiO3 as the precursor and using polystyrene and polystyrene-methyl acrylic acid latexes as the templates. The diameter and shell thickness of the hollow SiO2 spheres increase with increasing the latex template diameter at a given mass ratio of SiO2 to latex template. The diameter and shell thickness of the hollow SiO2 spheres also increase with increasing the mass ratios of SiO2 to latex template. The presence of carboxylic acid groups on the surfaces of polystyrene-methyl acrylic acid latex templates favors the formation of dense and uniform SiO2 shells. The hollow SiO2 sphere is constructed by mesoporous shell with large specific surface area. When glyphosate is used as a release model chemical, glyphosate release rate is tuned by varying the shell thickness.展开更多
Hydroxyl-epoxy phosphate （HEP） as a reactive corrosion inhibitor was innovatively synthe- sized by the reaction of bisphenol A epoxy resin with phosphoric acid. HEP was mixed with hydroxyl acrylate resin, and crossl...Hydroxyl-epoxy phosphate （HEP） as a reactive corrosion inhibitor was innovatively synthe- sized by the reaction of bisphenol A epoxy resin with phosphoric acid. HEP was mixed with hydroxyl acrylate resin, and crosslinked with waterborne isocyanate curing agent, which was used to form waterborne HEP/acrylic polyurethane composite （HEP-APU） coatings on Q235 steel surfaces. Electrochemical impedance spectroscopy and polarization curves were applied to analyze the corrosion behavior of the HEP-APU coatings in 3.5wt% NaCl solutions. The results indicated that the HEP-APU coatings show a superior passivation property and efficient corrosion protection of Q235 steel. The waterborne acrylic polyurethane coating containing 0.5wt% HEP exhibited the best corrosion performance among all the coating specimens. The improved flash-rust resistance can be attributed to the introduction of the phosphate group which could form phosphate film on the steel substrate.展开更多
Grafting of acrylic acid (AAc) and acrylamide (AAm) onto preirradiated PP film was performed in aqueous solution of AAc and AAm, respectively. Electron beam accelerator was used as irradiation source. The effect of f...Grafting of acrylic acid (AAc) and acrylamide (AAm) onto preirradiated PP film was performed in aqueous solution of AAc and AAm, respectively. Electron beam accelerator was used as irradiation source. The effect of ferrous sulfate, sodium nitrate, methanol and glucose on the degree of grafting was demonstrated. The function of the different additives was compared by the grafting of different monomers (AAc and AAm). The results show that the four of these additives are elective on the grafting of AAc. Only two of these additives, ferrous sulfate and methanol were effective on the grafting of AAm.展开更多
Copolymer of maleic acid and acrylic acid （PMA-100）, combining with polyvinyl butyral （PVB） ultrafiltration membrane was used for the removal of Mn（II） from waste water by complexation-ultrafiltration. The carbo...Copolymer of maleic acid and acrylic acid （PMA-100）, combining with polyvinyl butyral （PVB） ultrafiltration membrane was used for the removal of Mn（II） from waste water by complexation-ultrafiltration. The carboxylic group content of PMA-100 and the rate of complexation reaction were measured. Effects of the mass ratio of PMA-100 to Mn（II） （n）, pH, background electrolyte, etc on the rejection rate （R） and permeate flux （J） were investigated. The results show that carboxylic group content of PMA-100 is 9.5 mmol/g. The complexation of Mn（II） with PMA-100 is rapid and completed within 5 min at pH 6.0. Both R and J increase with pH increasing in the range of 2.5-7.0, and R increases with the increase of n at pH 6.0 while J is little affected. The background electrolyte leads to the decrease of R, and CaCl2 has much greater effect on R than NaCl at the same ionic strength.展开更多
Poly (EA-MAn-APTES)/silica hybrid materials were successfully prepared fromEthyl acrylate (EA), maleic anhydride (MAn) and tetraethoxysilane (TEOS) in the presence of acoupling agent 3-aminopropyltriethoxysilane (APTE...Poly (EA-MAn-APTES)/silica hybrid materials were successfully prepared fromEthyl acrylate (EA), maleic anhydride (MAn) and tetraethoxysilane (TEOS) in the presence of acoupling agent 3-aminopropyltriethoxysilane (APTES),by free-radical solution polymerization and insitu sol-gel process. The mass fraction of TEOS varied from 0 to 25%. The hybrid materials werecharacterized by the methods of FT-IR spectra, solvent extraction, scanning electron microscope (SEM), transmission electron microscope (TEM), differential scanning calorimetry (DSC) andthermogravimetric analysis (TGA) measuring apparatus to get their structures, gel contents,morphologies, particle sizes and thermal performances. The results show that the covalent bonds arebetween organic and inorganic phases, gel contents in the hybrid materials are much higher, theSiO_2 phase is well dispersed in the polymer matrix, silicon dioxide exist at nanoscale in thecomposites and have excellent thermal stability.展开更多
The products of thermal desorption were generated under the temperature of 280 ℃ and were analyzed by gas chromatography-mass spectrometry with capillary column,the residual monomer styrene was no detected.The produc...The products of thermal desorption were generated under the temperature of 280 ℃ and were analyzed by gas chromatography-mass spectrometry with capillary column,the residual monomer styrene was no detected.The products of pyrolysis were generated under the temperature of 550 ℃ and were analyzed by chromatography-mass spectrometry,14 compounds were detected.展开更多
A Aeries of hydroxylic hyperbranched polymers were derived from 2,2-bis(methylol) propionic acid and tris(methylol) propane reacted with acrylic acid to various extents. The obtained acrylated hyperbranched polymers a...A Aeries of hydroxylic hyperbranched polymers were derived from 2,2-bis(methylol) propionic acid and tris(methylol) propane reacted with acrylic acid to various extents. The obtained acrylated hyperbranched polymers alone or with a monofunctional diluent, isobornylene acrylate(IBOA) were further cured by UV radiation. The cured films based on the modified polymers alone all demonstrated poor mechanical properties due to their high network densities and low moving ability of polymer chains. For the composite systems, the cured films demonstrated improved mechanical properties due to the low network densities and high chain moving ability. With more IBOA included in the systems, acrylate groups can react to a higher extent during the curing process.展开更多
An attempt was made in the paper aiming at imparting flame retardancy to polymers by plasma grafting technique Based on EVA copolymers with different VA contents the author tried to use the Ar plasma followed by graf...An attempt was made in the paper aiming at imparting flame retardancy to polymers by plasma grafting technique Based on EVA copolymers with different VA contents the author tried to use the Ar plasma followed by grafting with/without subsequent saponification and metal ion exchange expediting the charring of polymers upon heationg Characterization of the flammability of the plasma treated EVA copolymers grafted with acrylic monomers(MAA,AA and AAm)indicates that this approach turns out to be a promising way and worthy doing whatever in research and/or applications展开更多
文摘Epoxy resin based Unsaturated poly(ester-amide) resins (UPEAs) can be prepared by many methods but here these were prepared by reported method [1]. These UPEAs were then treated with acrylotl chloride to afford acrylated UPEAs resin (i.e. AUPEAs). Interacting blends of equal proportional AUPEAs and vinyl ester epoxy (VE) resin were prepared. APEAs and AUPEAs were characterized by elemental analysis, molecular weight determined by vapour pressure osmometer and by IR spectral study and by thermogravimetry. The curing of interacting blends was monitored on differential scanning calorimeter (DSC). Based on DSC data in situ glass reinforced composites of the resultant blends have been prepared and characterized for mechanical, electrical and chemical properties. Unreinforced blends were characterized by thermogravimetry (TGA).
基金Fundamental Research Funds of CAF(No.CAFYBB2017QA017)Natural Science Foundation of Jiangsu Province(No.BK20161122)。
文摘A novel phosphorous-containing acrylated epoxidized soybean oil-based(P-AESO)resin was developed via the ring-opening reaction of epoxidized soybean oil(ESO)with diphenylphosphinic chloride(DPPC),followed by acrylation of the resulting groups.The chemical structure was characterized by Fourier transform infrared spectroscopy(FT-IR),and ^(1)H nuclear magnetic resonance(^(1)H NMR).Subsequently,the viscosity and volumetric shrinkage of the obtained P-AESO resins were studied.Then the oligomer was formulated into UV-curable coatings,and the mechanical,thermal,and coating properties of the resulting UV-cured bioresins were studied by tensile testing,dynamic mechanical thermal analysis(DMA),thermogravimetric analysis(TGA)coupled with FT-IR spectroscopy(TGA-FT-IR),hardness,adhesion,pencil hardness and chemical resistance.Furthermore,the UV-curing behavior of the P-AESO resin was determined by real-time realtime infrared(RT-IR).Meanwhile,compared with coating from acrylated epoxidized soybean oil(AESO),the P-AESO system coatings showed better volumetric shrinkage,excellent adhesion,and enhanced thermal and glass transition temperature(Tg)while maintaining reasonably final C=C conversions and cross-link density.For instance,the obtained P-AESO/trimethylolpropanetriacrylate(TMPTA)20 material possessed a volumetric shrinkage of 4.1%,Tg of 115.6℃,char yield of 9.47%,and final C=C conversions of 81.4%respectively,which exhibited superior values than that of the AESO/TMPTA20 material.The improvement of the P-AESO coating performances could contribute to the architectures that combined the structural features of phosphorous-containing rigid benzene.The developed P-AESO resin is promising for applications in the UV-curable coatings.
基金Funded by the National Natural Science Foundation of China(No.52473077)China Three Gorges Corporation(No.202403190)。
文摘In ultraviolet cured-in-place-pipe(UV-CIPP)pipeline rehabilitation,resin performance critically determines repair effectiveness.Current UV-curable resins exhibit high volatile organic compound(VOC)emissions and inadequate post-cure toughness,which compromise fatigue resistance during service.To address these issues,we synthesized hydroxyl-terminated polyurethane acrylate prepolymers using diphenylmethane diisocyanate(MDI),polypropylene glycol(PPG),and hydroxyethyl methacrylate(HEMA).Fourier transform infrared spectroscopy(FTIR)confirmed successful prepolymer synthesis.We developed UV-curable resins by incorporating various crosslinking monomers and optimized the formulations through mechanical property analysis.Testing revealed that the polyurethane-acrylic UV-cured resin system combines polyurethane's mechanical excellence with acrylics'high UV-curing activity.The PPG200/MDI/HEMA formulation achieved superior performance,with a tensile strength of 55.31 MPa,an impact toughness of 22.7 kJ/m^(2),and a heat deflection temperature(HDT)of 132℃.The optimized system eliminates volatile components while maintaining high reactivity,addressing critical limitations in trenchless pipeline rehabilitation.The improved mechanical properties meet the operational demands of underground pipes,suggesting practical applicability in trenchless pipeline repair.
基金supported by the National Natural Science Foundation of China(Nos.42277315,22066009)the Scientific Research Startup Fund of Hainan University(Nos.XJ2300005916,kyqd(zr)22185)+1 种基金supported by Scientific Research Project of Hainan Higher Education Institutions(No.Hnky2023-9)Innovational Fund for Scientific and Technological Personnel of Hainan Province(No.KJRC2023C12)。
文摘Synergy strategy of photocatalysts and polymer resins are promising technology for marine antifouling.However,it is still a main challenge to obtain a green,safe,and efficient antifouling coatings.Herein,carbon(graphene or CNT)modified Ti O_(2)photocatalyst was synthesized via hydrothermal and annealing process and has successfully applied in acrylate fluoroboron polymer(ABFP)composite coating.Morphology and chemical composition were detailed characterized.The graphene or CNT acted as a bridge with supplemental spatial structures(petal gaps,entanglement)and new functional groups(C-O,C-Ti-O,etc.)on Ti O_(2)particle.Carbon nanotube(CNT)modified TiO_(2)-ABFP coatings(BTCP)achieved excellent antibacterial and anti-diatom adhesion rate of 89.3%-96.70%and 99.00%-99.50%,which was 1.84-4.94-fold more than that of the single ABFP.CNT or graphene served as electronic bridges was considered as the crucial mechanism,which significantly improved the light absorption range and capacity,conductivity,and photoelectric response of Ti O_(2),and further accelerated the generation and transfer of free radicals to the surface of BTCP or FTGP.Moreover,the improvement of catalyst activity synergizes with the smooth surface,hydrophilicity,and slow hydrolysis of composite coatings,achieved long-term and efficient antifouling performance.This work provides a new insight into the modification of Ti O_(2)and antifouling mechanism of polymer coating.
基金Project supported by the State Key Laboratory of Geohazard Prevention and Geoenvironment Protection(SKLGP2020Z003)。
文摘A novel composite material,Poly(IL-AA)@MIL-101(Cr),combining metal-organic framework,polymeric ionic liquid and acrylic acid,was synthesized for the selective and efficient adsorption of rare earths europium(Ⅲ)(Eu3+).Characterization of the materials was carried out using techniques such as X-ray diffraction(XRD),Fourier transform infrared(FTIR),scanning electron microscopy-energy dispersive X-ray spectroscopy(SEM-EDS),thermogravimetric analysis(TGA)and Brunauer-Emmett-Teller(BET).The results demonstrate successful incorporation of the polymeric ionic liquid onto the material surface while preserving the crystal structure and mo rphology of MIL-101(Cr).Adsorption experiments were conducted to explore parameters including equilibrium pH,initial Eu3+concentration,and duration,with comprehensive analyses of adsorption kinetics,isotherms,and mechanisms.Findings reveal that Poly(IL1-AA)@MIL-101(Cr),Poly(IL3-AA)@MIL-101(Cr),and Poly(IL5-AA)@MIL-101(Cr)achieve adsorption equilibrium for Eu3+at approximately 9 h with an equilibrium pH of 6.2.The adso rption of Eu^(3+)predominantly follows a pseudo-second-order kinetic model and Langmuir isotherm adsorption model.Moreover,the prepared composite material exhibits superior adsorption selectivity for Eu^(3+)over other metal ions in the mixture(K^(+),Mg^(2+),Ni^(2+),Co^(2+),Zn^(2+),La^(3+),and Nd^(3+)).Even after five adsorption-desorption cycles,the composite material maintains satis factory adsorption performance.
基金Funded by the National Natural Science Foundation of China(No.51873167)the Self-determined and Innovative Research Funds of WUT(No.2024-CL-B1-02)。
文摘Modified activated carbons(AS)were fabricated through the oxidation effect of ammonium persulfate and applied to the dynamic adsorption of different acrylate gas.The pore structures,surface chemical properties and surface morphology of AS were respectively characterized by N2 adsorption,Boehm titration,X-ray Photoelectron Spectroscopy(XPS)and scanning electron microscopy(SEM)techniques.After modification,the specific surface area increased from 954 to 1154 m^(2)·g^(-1).The contents of oxygen-containing functional groups on the AS surface increase obviously and have a great effect on the adsorption behavior of acrylate gases.According to the results of dynamic adsorption,the adsorption capacities of acrylates are as the following order:methyl acrylate(461.9 mg·g^(-1))>methyl methacrylate(436.9 mg·g^(-1))>butyl acrylate(381.8 mg·g^(-1)),which is attributed to the size adaptability of AS pores and acrylates.The adsorption behavior of AS for acrylate gases conforms to the Bangham model and the Temkin model.
基金supported by the National Natural Science Foundation of China(No,22271074)Natural Science Foundation of Hebei Province(Nos.B2023208042,B2022208032,B2021208066,E2024208084 , E2024208088)+2 种基金Science Research Project of Hebei Education Department(No.JZX2024013)Special Fund for Local Scientific and Technological Development under the Guidance of the Central Government(No.236Z3704G)Hebei Province High Level Talent Funding(No.A202001010).
文摘Flexible wearable electronic devices based on hydrogels have immense potential in a wide range of applications.However,many existing strain sensors suffer from significant limitations including poor mechanical properties,low adhesion,and insufficient conductivity.To address these challenges,this study successfully developed an organic-inorganic double-network conductive hydrogel using acrylic-modified bentonite (AABT) as a key component.The incorporation of AABT significantly enhanced the mechanical properties of the ATHG@LiCl hydrogel,achieving an impressive stretchability of 4000% and tensile strength of 250 kPa.Moreover,it improved the electrical conductivity of the hydrogel to a maximum of 1.53 mS/cm.The catechol structure of tannic acid (TA) further augmented the adhesive properties of the ATHG@LiCl hydrogel toward various substrates such as copper,iron,glass,plastic,wood,and pigskin.The addition of lithium chloride (LiCl) and dimethyl sulfoxide(DMSO) endowed the hydrogel with exceptional freezing resistance and flexibility,even at low temperatures of-20℃.Remarkably,the hydrogel maintained a conductivity of 0.53 mS/cm under these conditions,surpassing the performance of many other reported hydrogels.Furthermore,the ATHG@LiCl hydrogel demonstrated outstanding characteristics,such as high sensitivity (gauge factor GF=4.50),excellent transparency (90%),and reliable strain-sensing capabilities,indicating that the ATHG@LiCl hydrogel is a highly promising candidate for flexible wearable soft materials,offering significant advancements in both functionality and performance.
文摘Vanadium phosphorus oxide(VPO)catalyst is a promising candidate for the condensation reaction of formaldehyde(FA)and acetic acid(HAc)to produce acrylic acid(AA).However,the complexity of the active phases and their dynamic interconversion under redox conditions has led to controversies regarding the actual active phase in this reaction.To address this,this study systematically investigates the phase transition and underlying mechanism of VPO catalysts under reaction conditions.X-ray diffraction(XRD)patterns,Raman spectra,transmission electron microscopy images and X-ray photoelectron spectroscopy collectively demonstrated that the V^(4+)phase(VO)_(2)P_(2)O_(7)retained the bulk phase structure throughout the reaction,with only minor surface phase transition observed.In contrast,the V^(5+)phase underwent reduction to other phases in both bulk and surface regions.Specifically,theδ-VOPO_(4)phase rapidly transformed into theαII-VOPO_(4)phase,which could reversibly convert into the R1-VOHPO_(4)phase(V^(4+)).Controlled variable experiments,H_(2)-temperature programmed reduction and in-situ XRD experiments in a hydrogen atmosphere further demonstrated that these phase transitions were primarily attributed to the loss of lattice oxygen.The presence of V^(4+)phase in VPO catalysts enhanced the selectivity of acrylic acid,while the existence of V^(5+)phase promoted the activation of acetic acid.This work elucidates the redox-driven phase evolution of VPO catalysts and offers valuable insights for designing efficient catalysts for FA-HAc cross-condensation by balancing phase stability and activity.
文摘Toray Industries,Inc.announced that from this April,it will im-plement the mass balance approach in manufacturing its TORAY-LON TMacrylic staple fiber.This method attributes properties fromboth biomass and plastic waste,contributing to sustainabillty.Thecompany has already secured ISCC(nternational Sustainability&Carbon Certification)PLUScertification for this initiative.
基金supported by the National Natural Science Foundation of China(52473059)Taishan Scholar Constructive Engineering Foundation of Shandong Province(tsqn202103079)Key Research and Development Plan of Shandong Province(2024TSGC0264).
文摘Power cables are important pieces of equipment for energy transmission,but achieving a good balance between flame retardancy and mechanical properties of cable sheaths remains a challenge.In this work,a novel intumescent flame retardant(IFR)system containing silicone-containing macromolecular charring agent(Si-MCA)and ammonium polyphosphate(APP)was designed to synergistically improve the flame retardancy and mechanical properties of ethylene-butyl acrylate copolymer(EBA)composites.The optimal mass ratio of APP/Si-MCA was 3/1 in EBA composites(EBA/APP-Si-31),corresponding to the best flame retardancy with 31.2% of limited oxygen index(LOI),V-0 rating in UL-94 vertical burning test,and 76.4%reduction on the peak of heat release rate(PHRR)in cone calorimeter test.The enhancement mechanism was attributed to the synergistic effect of APP/Si-MCA during combustion,including the radical-trapping effect,the dilution effect of non-flammable gases,and the barrier effect of the intumescent char layer.Meanwhile,the tensile results indicated that EBA/APP-Si-31 also exhibited good mechanical properties with the addition of maleic anhydride-grafted polyethylene(PE-g-MA)as the compatibilizer.Thus,the APP/Si-MCA combination is an effective IFRs system for preparing high-performance EBA composites,and it will promote their applications as cable sheath materials.
基金financially supported by the Science and Technology Commission of Shanghai Municipality(No.24ZR1401400)Shenzhen Salus Bio Med Company for their strong support in this study。
文摘In this study,an amine-reactive poly(pentafluorophenyl acrylate)(PPFPA)platform was developed for advanced surface engineering of next-generation sequencing(NGS)chips.Through post-polymerization modification,PPFPA was functionalized with dual moieties:azide groups for covalent immobilization of DBCO-modified DNA primers via click chemistry and tunable hydrophilic side chains to optimize biocompatibility and surface properties.Systematic screening revealed that hydrophobic azide carriers combined with neutral hydroxyl groups maximized the DNA immobilization efficacy,approaching the performance of commercial polyacrylamide-based polymers.The negatively charged carboxyl groups severely impede DNA primer attachment.Higher molecular weight derivatives further enhance the efficacy of DNA immobilization.In NGS validation,optimized surface modification polymers achieved robust surface density of clustered DNA and high sequencing accuracy,surpassing quality benchmarks and comparable to those of conventional analogs.This platform demonstrates significant potential for tailoring high-sensitivity surfaces for genomic applications,advancing clinical diagnostics,and personalized medicine.
基金Projects (11KJB530002, CX10B-259Z) supported by Research Funds from Jiangsu Provincial Department of Education, ChinaProject (10zxfk35) supported by Sichuan Province Nonmetallic Composites and Functional Materials Key Laboratory Project, China
文摘Different-sized hollow SiO2 spheres of 249–1348 nm in diameter were successfully prepared by using Na2SiO3 as the precursor and using polystyrene and polystyrene-methyl acrylic acid latexes as the templates. The diameter and shell thickness of the hollow SiO2 spheres increase with increasing the latex template diameter at a given mass ratio of SiO2 to latex template. The diameter and shell thickness of the hollow SiO2 spheres also increase with increasing the mass ratios of SiO2 to latex template. The presence of carboxylic acid groups on the surfaces of polystyrene-methyl acrylic acid latex templates favors the formation of dense and uniform SiO2 shells. The hollow SiO2 sphere is constructed by mesoporous shell with large specific surface area. When glyphosate is used as a release model chemical, glyphosate release rate is tuned by varying the shell thickness.
文摘Hydroxyl-epoxy phosphate （HEP） as a reactive corrosion inhibitor was innovatively synthe- sized by the reaction of bisphenol A epoxy resin with phosphoric acid. HEP was mixed with hydroxyl acrylate resin, and crosslinked with waterborne isocyanate curing agent, which was used to form waterborne HEP/acrylic polyurethane composite （HEP-APU） coatings on Q235 steel surfaces. Electrochemical impedance spectroscopy and polarization curves were applied to analyze the corrosion behavior of the HEP-APU coatings in 3.5wt% NaCl solutions. The results indicated that the HEP-APU coatings show a superior passivation property and efficient corrosion protection of Q235 steel. The waterborne acrylic polyurethane coating containing 0.5wt% HEP exhibited the best corrosion performance among all the coating specimens. The improved flash-rust resistance can be attributed to the introduction of the phosphate group which could form phosphate film on the steel substrate.
文摘Grafting of acrylic acid (AAc) and acrylamide (AAm) onto preirradiated PP film was performed in aqueous solution of AAc and AAm, respectively. Electron beam accelerator was used as irradiation source. The effect of ferrous sulfate, sodium nitrate, methanol and glucose on the degree of grafting was demonstrated. The function of the different additives was compared by the grafting of different monomers (AAc and AAm). The results show that the four of these additives are elective on the grafting of AAc. Only two of these additives, ferrous sulfate and methanol were effective on the grafting of AAm.
基金Project (21176264) supported by the National Natural Science Foundation of ChinaProject (11JJ2010) supported by Hunan Provincial Natural Science Foundation of ChinaProject (LC13076) supported by Undergraduate Innovation Foundation of Central South University,China
文摘Copolymer of maleic acid and acrylic acid （PMA-100）, combining with polyvinyl butyral （PVB） ultrafiltration membrane was used for the removal of Mn（II） from waste water by complexation-ultrafiltration. The carboxylic group content of PMA-100 and the rate of complexation reaction were measured. Effects of the mass ratio of PMA-100 to Mn（II） （n）, pH, background electrolyte, etc on the rejection rate （R） and permeate flux （J） were investigated. The results show that carboxylic group content of PMA-100 is 9.5 mmol/g. The complexation of Mn（II） with PMA-100 is rapid and completed within 5 min at pH 6.0. Both R and J increase with pH increasing in the range of 2.5-7.0, and R increases with the increase of n at pH 6.0 while J is little affected. The background electrolyte leads to the decrease of R, and CaCl2 has much greater effect on R than NaCl at the same ionic strength.
文摘Poly (EA-MAn-APTES)/silica hybrid materials were successfully prepared fromEthyl acrylate (EA), maleic anhydride (MAn) and tetraethoxysilane (TEOS) in the presence of acoupling agent 3-aminopropyltriethoxysilane (APTES),by free-radical solution polymerization and insitu sol-gel process. The mass fraction of TEOS varied from 0 to 25%. The hybrid materials werecharacterized by the methods of FT-IR spectra, solvent extraction, scanning electron microscope (SEM), transmission electron microscope (TEM), differential scanning calorimetry (DSC) andthermogravimetric analysis (TGA) measuring apparatus to get their structures, gel contents,morphologies, particle sizes and thermal performances. The results show that the covalent bonds arebetween organic and inorganic phases, gel contents in the hybrid materials are much higher, theSiO_2 phase is well dispersed in the polymer matrix, silicon dioxide exist at nanoscale in thecomposites and have excellent thermal stability.
文摘The products of thermal desorption were generated under the temperature of 280 ℃ and were analyzed by gas chromatography-mass spectrometry with capillary column,the residual monomer styrene was no detected.The products of pyrolysis were generated under the temperature of 550 ℃ and were analyzed by chromatography-mass spectrometry,14 compounds were detected.
基金Supported by the National Natural Science Foundation of China(No.2 0 2 0 4 0 0 5 ,5 0 2 330 30 ) and Basic Research Fund ofTsinghua University(No.JC2 0 0 2 0 30 )
文摘A Aeries of hydroxylic hyperbranched polymers were derived from 2,2-bis(methylol) propionic acid and tris(methylol) propane reacted with acrylic acid to various extents. The obtained acrylated hyperbranched polymers alone or with a monofunctional diluent, isobornylene acrylate(IBOA) were further cured by UV radiation. The cured films based on the modified polymers alone all demonstrated poor mechanical properties due to their high network densities and low moving ability of polymer chains. For the composite systems, the cured films demonstrated improved mechanical properties due to the low network densities and high chain moving ability. With more IBOA included in the systems, acrylate groups can react to a higher extent during the curing process.
文摘An attempt was made in the paper aiming at imparting flame retardancy to polymers by plasma grafting technique Based on EVA copolymers with different VA contents the author tried to use the Ar plasma followed by grafting with/without subsequent saponification and metal ion exchange expediting the charring of polymers upon heationg Characterization of the flammability of the plasma treated EVA copolymers grafted with acrylic monomers(MAA,AA and AAm)indicates that this approach turns out to be a promising way and worthy doing whatever in research and/or applications
