It is important to understand the evolution of the matter on the polymer membrane surface.The in situ and real-time monitoring of the membrane surface will not only favor the investigation of selective layer formation...It is important to understand the evolution of the matter on the polymer membrane surface.The in situ and real-time monitoring of the membrane surface will not only favor the investigation of selective layer formation but can also track the fouling process during operation.Herein,an aggregation-induced emission(AIE)-active polymer membrane was prepared by the interfacial polymerization of a cyclodextrin-based glycocluster(CD@Glucose)and a tetraphenylethylene derivative modified with boronic acid groups(TPEDB)on the surface of a polyacrylonitrile(PAN)ultrafiltration membrane.This interfacial polymerization method can be stacked layer-by-layer to regulate the hydrophilicity and pore structure of the membrane.With the increase in the number of polymer layers,the separation and antifouling properties of the membrane gradually improved.Owing to the AIE property of the crosslinking agent TPEDB,the occurrence of interfacial polymerization and the degree of fouling during membrane operation can be monitored by the fluorescence distribution and intensity.With the aggravation of membrane fouling,the fluorescence decreased gradually,but recovered after cleaning.Therefore,this AIE effect can be used for real-time monitoring of interfacial polymerization as well as membrane fouling.展开更多
The preparation of composite charge-mosaic membrane included spinning of hollow fiber as the supporting membrane, preparing a selective layer on the inside surface of the fiber by interfacial polymerization. The char...The preparation of composite charge-mosaic membrane included spinning of hollow fiber as the supporting membrane, preparing a selective layer on the inside surface of the fiber by interfacial polymerization. The charge-mosaic membranes show a high salt permeability while retaining sucrose. The charge-mosaic membrane can be effectively used to separate multivalent salts with organic matter of molecular weight great than 300 g/mol in industry.展开更多
The high-efficiency fabrication of high-quality microcapsules containing epoxy is crucial to the further development of the potential practical self-healing epoxy systems based on microencapsulated two-part epoxy-amin...The high-efficiency fabrication of high-quality microcapsules containing epoxy is crucial to the further development of the potential practical self-healing epoxy systems based on microencapsulated two-part epoxy-amine chemistry.Herein,a novel microencapsulation technique based on non-equilibrium droplets via integrating electrospraying and interfacial polymerization(ES-IP)was established to efficiently microencapsulate epoxy monomers.The ES-IP technique,consisting of three continuous steps,i.e.electrospraying to massively generate droplets,enwrapping every single droplet through instant interfacial polymerization,and thickening shell at an elevated temperature,has great flexibility to regulate the microencapsulation process and the microcapsule quality.The fabricated core-shell structured epoxy microcapsules(Ep-MCs)were comprehensively characterized for their properties,showing that they have high cleanness with rare impurities,controllable and tunable size,good thermal stability and tightness,and high effective core fraction.The high-quality Ep-MCs were adopted to formulate a self-healing epoxy based on the microencapsulated epoxy-amine chemistry.The highest healing efficiency,in terms of the recovered mode I fracture toughness,of 110±17%was achieved after being healed at room temperature(~25℃)for 48 h.While the developed ES-IP technique facilitates the microencapsulation technique based on non-equilibrium droplets,the fabricated high-quality Ep-MCs greatly promote the further developments of the practical self-healing materials.展开更多
Polyamide(PA)-based thin-film composite membranes exhibit enormous potential in water purification,owing to their facile fabrication,decent performance and desirable stability.However,the thick PA active layer with hi...Polyamide(PA)-based thin-film composite membranes exhibit enormous potential in water purification,owing to their facile fabrication,decent performance and desirable stability.However,the thick PA active layer with high transport resistance from the conventional interfacial polymerization hampers their applications.The controllable fabrication of a thin PA active layer is essential for high separation efficiency but still challenging.Herein,a covalent organic framework TpPa-1 interlayer was firstly deposited on a polyethersulfone(PES)substrate to reduce the thickness of PA active layer in interfacial polymerization.The abundant pores of TpPa-1 increase the local concentration of amine monomers by adsorbing piperazine molecules,while hydrogen bonds between hydrophilic groups of TpPa-1 and piperazine molecules slow down their diffusion rate.Arising from those synergetic effects,the PA active layer is effectively reduced from 200 nm to 120 nm.By optimizing TpPa-1 interlayer and PA active layer,the water flux of resultant membranes can reach 171.35 L·m^-2·h^-1·MPa^-1,which increased by 125.4%compared with PA/PES membranes,while the rejection rates of sodium sulfate and dyes solution remained more than 90%and 99%,respectively.Our strategy may stimulate rational design of ultrathin PA-based nanofiltration membranes with high performances.展开更多
Carbon dioxide(CO_2) is greenhouse gas which originates primarily as a main combustion product of biogas and landfill gas. To separate this gas, an inside coated thin film composite(TFC) hollow fiber membrane was deve...Carbon dioxide(CO_2) is greenhouse gas which originates primarily as a main combustion product of biogas and landfill gas. To separate this gas, an inside coated thin film composite(TFC) hollow fiber membrane was developed by interfacial polymerization between 1,3–cyclohexanebis–methylamine(CHMA) and trimesoyl chloride(TMC). ATR-FTIR, SEM and AFM were used to characterize the active thin layer formed inside the PSf hollow fiber. The separation behavior of the CHMA-TMC/PSf membrane was scrutinized by studying various effects like feed gas pressure and temperature. Furthermore, the influence of CHMA concentration and TMC concentration on membrane morphology and performance were investigated. As a result, it was found that mutually the CHMA concentration and TMC concentration play key roles in determining membrane morphology and performance. Moreover, the CHMA-TMC/PSf composite membrane showed good CO_2/CH_4 separation performance. For CO_2/CH_4 mixture gas(30/70 by volume) test, the membrane(PD1 prepared by CHMA 1.0% and TMC 0.5%) showed a CO_2 permeance of 25 GPU and the best CO_2/CH_4 selectivity of 28 at stage cut of 0.1. The high CO_2/CH_4 separation performance of CHMA-TMC/PSf thin film composite membrane was mostly accredited to the thin film thickness and the properties of binary amino groups.展开更多
A new aromatic diamine,3,5-diaminobenzoylpiperazine （3,5-DABP）,was synthesized from 3,5-diaminobenzoic acid and 1-formyl piperazine.The structure of 3,5-DABP was identified by FT-IR spectra and 1H NMR spectra.With 3...A new aromatic diamine,3,5-diaminobenzoylpiperazine （3,5-DABP）,was synthesized from 3,5-diaminobenzoic acid and 1-formyl piperazine.The structure of 3,5-DABP was identified by FT-IR spectra and 1H NMR spectra.With 3,5-DABP as aqueous monomer and trimesoyl chloride （TMC） as organic monomer,thin film composite （TFC） nanofiltration membranes were prepared by interfacial polymerization technology.The salt rejection order of these TFC membranes is Na2SO4MgSO4MgCl2NaCl.This sequence indicates that the membranes are negatively charged.展开更多
Thin film composite(TFC)membranes with nanofillers additives for CO_(2)separation show promising applications in energy and environment-related fields.However,the poor compatibility between nanofillers and polymers in...Thin film composite(TFC)membranes with nanofillers additives for CO_(2)separation show promising applications in energy and environment-related fields.However,the poor compatibility between nanofillers and polymers in TFC membranes is the main problem.In this work,covalent organic frameworks(COFs,TpPa-1)with rich ANHA groups were incorporated into polyamide(PA)segment via in situ interfacial polymerization to prepare defect-free TFC membranes for CO_(2)/N_(2)separation.The formed covalent bonds between TpPa-1 and PA strengthen the interaction between nanofillers and polymers,thereby enhancing compatibility.Besides,the incorporated COFs disturb the rigid structure of the PA layer,and provide fast CO_(2)transfer channels.The incorporated COFs also increase the content of effective carriers,which enhances the CO_(2)facilitated transport.Consequently,in CO_(2)/N_(2)mixed gas separation test,the optimal TFC(TpPa_(0.025)-PIP-TMC/m PSf)membrane exhibits high CO_(2)permeance of 854 GPU and high CO_(2)/N_(2)selectivity of 148 at 0.15 MPa,CO_(2)permeance of 456 GPU(gas permeation unit)and CO_(2)/N_(2)selectivity of 92 at 0.5 MPa.In addition,the Tp Pa_(0.025)-PIP-TMC/m PSf membrane also achieves high permselectivty in CO_(2)/CH_(4)mixed gas separation test.Finally,the optimal TFC membrane showes good stability in the simulated flue gas test,revealing the application potential for CO_(2)capture from flue gas.展开更多
A novel NF membrane prepared with poly（amidoamine） （PAMAM） dendrimer and trimesoyl chloride （TMC） by interfacial polymerization on polysulfone （PSF） ultrafiltration membrane was investigated. Field emission sc...A novel NF membrane prepared with poly（amidoamine） （PAMAM） dendrimer and trimesoyl chloride （TMC） by interfacial polymerization on polysulfone （PSF） ultrafiltration membrane was investigated. Field emission scanning electron microcopy （ FESEM）, atomic force micrograph （ AFM ） and contact angle （CA） of pure water on PA and PSF substrate were employed to characterize the chemical and physical properties of membranes. The PAMAM concentration, retention of salt solutions and organics were studied on the performance of the NF membrane. From the analyses of SEM and AFM, the polyamide active skin layers of the composite membranes are dense, rough, and finely dispersed nodular structures, packed tightly by the spherical globules. The contact angle of PA nanofitration membrane decreased after polymerization. The higher PAMAM concentra- tion can result in lower flux and higher rejection. The salt rejection of PA membranes decreases in the order K2 SO4 〉 Na2 SO4 〉 MgSQ 〉 MgC12 〉 CaC12 〉 NaC1, which indicates that the resulting membranes is nagatively charged. The pH increases from 3 to 10 in the feed resulting in the decrease of the flux and the increase of the rejection for NazSO4 solution. The molecular weight cut off （MWCO） of the composite NF membrane is nearly 860 kg/mol. The resulted PA membrane can be used to seoarate small organics and salt solutions.展开更多
A polyurea-chlorocyclophosphazene microcapsule flame retardant is prepared by an interfacial polymerization process using 2,4-toluene diisocyanate (TDI) and hexanediamine as the raw materials. TG tests show that the t...A polyurea-chlorocyclophosphazene microcapsule flame retardant is prepared by an interfacial polymerization process using 2,4-toluene diisocyanate (TDI) and hexanediamine as the raw materials. TG tests show that the thermal decomposition temperature of chlorocyclophosphazene in microcapsule obviously rises. The flame retardancy of HDPE/chlorocyclophosphazene in microencapsules is better than that of HDPE/chlorocyclophosphazene. Mechanical properties of HDPE/chlorocyclophosphazene microencapsule turn out to be superior to those of HDPE/chlorocyclophosphazene.展开更多
Enhancing the water permeation while maintaining high salt rejection of existing reverse osmosis(RO)membranes remains a considerable challenge.Herein,we proposed to introduce polymer of intrinsic microporosity,PIM-1,i...Enhancing the water permeation while maintaining high salt rejection of existing reverse osmosis(RO)membranes remains a considerable challenge.Herein,we proposed to introduce polymer of intrinsic microporosity,PIM-1,into the selective layer of reverse osmosis membranes to break the trade-off effect between permeability and selectivity.A water-soluble a-LPIM-1 of low-molecular-weight and hydroxyl terminals was synthesized.These designed characteristics endowed it with high solubility and reactivity.Then it was mixed with m-phenylenediamine and together served as aqueous monomer to react with organic monomer of trimesoyl chloride via interfacial polymerization.The characterization results exhibited that more“nodule”rather than“leaf”structure formed on RO membrane surface,which indicated that the introduction of the high free-volume of a-LPIM-1 with three dimensional twisted and folded structure into the selective layer effectively caused the frustrated packing between polymer chains.In virtue of this effect,even with reduced surface roughness and unchanged layer thickness,the water permeability of prepared reverse osmosis membranes increased 2.1 times to 62.8 L·m^(-2)·h^(-1) with acceptable Na Cl rejection of 97.6%.This attempt developed a new strategy to break the trade-off effect faced by traditional polyamide reverse osmosis membranes.展开更多
Although a great progress has been achieved for the development of NF membranes and technologies and SRNF do show a great potential in the separation of organic components, an NF membrane with good separation performa...Although a great progress has been achieved for the development of NF membranes and technologies and SRNF do show a great potential in the separation of organic components, an NF membrane with good separation performance and good resistance to organic solvents are urgently needed for a more complicated situation in practical. In this study, a kind of solvent-resistant nanofiltration (SRNF) membrane was fabricated via interfacial polymerization on a laboratory optimized cellulose acetate (CA) basic membrane. The effects of interfacial polymerization parameters, such as water phase concentration, immersed time in the water phase and in the organic phase, on the pure water flux and rejection rate of C-2R yellow dyestuffs were investigated. A highest dye rejection rate of 72.9% could be obtained by water phase solution containing 1% m-xylylenediamine (mXDA) and organic phase solution with 0.2% trimesoyl chloride (TMC) under immersed time in water phase of 6 minutes and in organic phase of 40 seconds. This membrane demonstrated better resistance to methyl alcohol compared to commercial membrane. This study may offer an avenue to develop a solvent-resistant nanofiltration membrane.展开更多
The surface and interfacial properties of polymeric bonding agents and nitramine crystal fillers were studied. The surface free energy and adhesion work of polymeric bonding agents and nitramine fillers were calculate...The surface and interfacial properties of polymeric bonding agents and nitramine crystal fillers were studied. The surface free energy and adhesion work of polymeric bonding agents and nitramine fillers were calculated by using Kaeble′s equations. It was observed that the hydroxyl values of neutral polymeric bonding agents (NPBA) correlate well with the polar components of surface free energies. On the basis of the measurements of swelling ratio and initial modulus, the interfacial bonding through highly crosslinked polymeric shell formation around the nitramine particles and generating interfacial reinforcement were rationalized. The application of Tapping Mode AFM (atomic force micro scope) to observing the surface morphology of NPBA reveals that methyl acrylate monomer appears to play a role for aiding the formation of network like structure when nanometer scale images of NPBA are created.展开更多
Rapid development of energy,electrical and electronic technologies has put forward higher requirements for the thermal conductivities of polymers and their composites.However,the thermal conductivity coefficient(λ)va...Rapid development of energy,electrical and electronic technologies has put forward higher requirements for the thermal conductivities of polymers and their composites.However,the thermal conductivity coefficient(λ)values of prepared thermally conductive polymer composites are still difficult to achieve expectations,which has become the bottleneck in the fields of thermally conductive polymer composites.Aimed at that,based on the accumulation of the previous research works by related researchers and our research group,this paper proposes three possible directions for breaking through the bottlenecks:(1)preparing and synthesizing intrinsically thermally conductive polymers,(2)reducing the interfacial thermal resistance in thermally conductive polymer composites,and(3)establishing suitable thermal conduction models and studying inner thermal conduction mechanism to guide experimental optimization.Also,the future development trends of the three above-mentioned directions are foreseen,hoping to provide certain basis and guidance for the preparation,researches and development of thermally conductive polymers and their composites.展开更多
Poly(p-phenylene-2,6-benzobisoxazole)(PBO)fibers possess excellent dielectric,mechanical properties and heat resistance.However,the surface of PBO fibers is smooth and highly chemical inert,resulting in poor interfaci...Poly(p-phenylene-2,6-benzobisoxazole)(PBO)fibers possess excellent dielectric,mechanical properties and heat resistance.However,the surface of PBO fibers is smooth and highly chemical inert,resulting in poor interfacial compatibility to polymer matrix,which severely limits its wider application in high-performance fiber-reinforced resin matrix composites.In this work,random copolymers(P(S-co-BCB-co-MMA))containing benzocyclobutene in the side-chain were synthesized by reversible addition-fragmentation chain transfer(RAFT)polymerization,which were then utilized to form dense random copolymer membrane on the surface of PBO fibers by thermally cross-linking at 250°C(PBO@P fibers).Four kinds of synthesized P(S-co-BCB-co-MMA)with different number-average molar mass(Mn)were well controlled and possessed narrow dispersity.When the Mnwas 32300,the surface roughness of PBO@P fibers was increased from 11 nm(PBO fibers)to 39 nm.In addition,PBO@P fibers presented the optimal interfacial compatibility with bisphenol A cyanate(BADCy)resins.And the single fiber pull-out strength of PBO@P fibers/BADCy micro-composites was 4.5 MPa,increasing by 45.2%in comparison with that of PBO fibers/BADCy micro-composites(3.1 MPa).Meantime,PBO@P fibers still retained excellent tensile strength(about 5.1 GPa).Overall,this work illustrates a simple and efficient surface functionalization method,which would provide a strong theoretical basis and technical support for controlling the surface structure&chemistry of inert substrates.展开更多
H+ doped polyaniline nanofibre(PH) was synthesized by interfacial polymerization and polyanilines doped with Li salt(PLI and PHLI) were prepared by immersing emeraldine base(EB) and H+ doped polyaniline in 1 mol/L LiP...H+ doped polyaniline nanofibre(PH) was synthesized by interfacial polymerization and polyanilines doped with Li salt(PLI and PHLI) were prepared by immersing emeraldine base(EB) and H+ doped polyaniline in 1 mol/L LiPF6/(EC-EMC-DMC),respectively.PH,PLI and PHLI were all characterized by scanning electron microscopy(SEM) and Fourier transform infrared(FT-IR) spectrometry.With 1 mol/L LiPF6/(EC-EMC-DMC) as electrolyte,PH,PHLI and PLI were used as the active materials of symmetric non-aqueous redox supercapacitors.PLI shows the highest initial specific capacitance of 120 F/g(47 F/g for PH and 66 F/g for PHLI) among three samples.After 500 cycles,the specific capacitance of PLI remains 75 F/g,indicating the good cycleability.展开更多
The stability of ultrathin polymer films plays a crucial role in their technological applications.Here,we systematically investigated the influence of interfacial adsorption in physical aging and the stability of thin...The stability of ultrathin polymer films plays a crucial role in their technological applications.Here,we systematically investigated the influence of interfacial adsorption in physical aging and the stability of thin polymer films in the solvent-induced process.We further identify the stability mechanism from the theory of thin film stability.Our results show that the aging temperature and film thickness can strongly influence the stability of thin PS films in acetone vapor.Physical aging can greatly improve the stability of thin polymer films when the aging temperature T_(aging1)>T_(g).A thinner PS film more quickly reaches a stable state via physical aging.At short aging time,the formation of the adsorbed layer can reduce the polar interaction;however,it slightly influences the stability of thin polymer films in the solvent-induced process.At later aging stage,the conformational rearrangement of the polymer chains induced by the interfacial effect at the aging temperature Taging1 plays an important role in stabilizing the thin polymer films.However,at T_(aging2)<T_(g),the process of physical aging slightly influences the stability of the thin polymer films.The formation of the adsorbed layer at Taging2 can reduce the short-range polar interaction of the thin film system and cannot suppress the instability of thin polymer films in the solvent-induced process.These results provide further insight into the stable mechanism of thin polymer films in the solvent-induced process.展开更多
Immiscible polymer blends are an important family of polymer materials.The interfacial thickness between different phases is a very important parameter that dictates,to a great extent,the morphology and properties of ...Immiscible polymer blends are an important family of polymer materials.The interfacial thickness between different phases is a very important parameter that dictates,to a great extent,the morphology and properties of such a blend.This work explores and optimizes an up-to-date atomic force microscopy(AFM)of type NanoIR2^(TM) system in order to quantitatively measure the interfacial thickness of immiscible polymer blends.This system is equipped with two nano-probes capable of detecting the response of a material to an infrared pulse called AFM-infrared spectroscopy mode(AFM-IR)or conducting resonance called AFM-Lorentz Contact Resonance mode(AFM-LCR),respectively.Its potential for quantitatively measuring the interfacial thickness of immiscible polymer blends is evaluated using blends composed of polyamide 6(PA6)and polyolefin elastomer(POE)in the presence or absence of a POE containing maleic anhydride(POE-g-MAH)as a compatibilizer.Surface roughness affects adversely the signal intensity and consequently an accurate measurement of the interfacial thickness.Optimum sample surface preparation procedures are proposed.展开更多
The solid-state lithium battery is considered as an ideal next-generation energy storage device owing to its high safety,high energy density and low cost.However,the poor ionic conductivity of solid electrolyte and lo...The solid-state lithium battery is considered as an ideal next-generation energy storage device owing to its high safety,high energy density and low cost.However,the poor ionic conductivity of solid electrolyte and low interfacial stability has hindered the application of solid-state lithium battery.Here,a flexible polymer/garnet solid electrolyte is prepared with poly(ethylene oxide),poly(vinylidene fluoride),Li6.75La3 Zr1.75Ta0.25O12,lithium bis(trifluoromethanesulfonyl)imide and oxalate,which exhibits an ionic conductivity of 2.0 ×10^(-4) S cm^(-1) at 55℃,improved mechanical property,wide electrochemical window(4.8 V vs.Li/Li+),enhanced thermal stabilities.Tiny acidic OX was introduced to inhibit the alkalinity reactions between Li6.75La3 Zr1.75Ta0.25O12 and poly(vinylidene fluoride).In order to improve the interfacial stability between cathode and electrolyte,an Al2 O3@LiNi0.5Co0.2Mn0.3O2 based composite cathode framework is also fabricated with poly(ethylene oxide) polymer and lithium salt as additives.The solid-state lithium battery assembled with polymer/garnet solid electrolyte and composite cathode framework demonstrates a high initial discharge capacity of 150.6 mAh g^(-1) and good capacity retention of 86.7% after 80 cycles at 0.2 C and 55℃,which provides a promising choice for achieving the stable electrode/electrolyte interfacial contact in solid-state lithium batteries.展开更多
The weak interface interaction and solid-solid phase transition have long been a conundrum for 1,3,5,7-tetranitro-1,3,5,7-tetraazacyclooctane(HMX)-based polymer-bonded explosives(PBX).A two-step strategy that involves...The weak interface interaction and solid-solid phase transition have long been a conundrum for 1,3,5,7-tetranitro-1,3,5,7-tetraazacyclooctane(HMX)-based polymer-bonded explosives(PBX).A two-step strategy that involves the pretreatment of HMX to endow—OH groups on the surface via polyalcohol bonding agent modification and in situ coating with nitrate ester-containing polymer,was proposed to address the problem.Two types of energetic polyether—glycidyl azide polymer(GAP)and nitrate modified GAP(GNP)were grafted onto HMX crystal based on isocyanate addition reaction bridged through neutral polymeric bonding agent(NPBA)layer.The morphology and structure of the HMX-based composites were characterized in detail and the core-shell structure was validated.The grafted polymers obviously enhanced the adhesion force between HMX crystals and fluoropolymer(F2314)binder.Due to the interfacial reinforcement among the components,the two HMX-based composites exhibited a remarkable increment of phase transition peak temperature by 10.2°C and 19.6°C with no more than 1.5%shell content,respectively.Furthermore,the impact and friction sensitivity of the composites decreased significantly as a result of the barrier produced by the grafted polymers.These findings will enhance the future prospects for the interface design of energetic composites aiming to solve the weak interface and safety concerns.展开更多
Mixing two or more polymers to produce the“polymer alloy”is one of the most versatile and economical strategies for developing new polymeric materials.The compatibility between polymer components largely determines ...Mixing two or more polymers to produce the“polymer alloy”is one of the most versatile and economical strategies for developing new polymeric materials.The compatibility between polymer components largely determines the comprehensive performance of polymer blend.More recently,a type of unique surface partitioned materials,Janus particles,has been proposed to act as a novel interfacial compatibilizer for polymer blends.Such Janus particles integrates the amphipathicity of diblock copolymer and interfacial stabilization of nanoparticles,displaying a significant superiority in comparison with molecular compatibilizers for a wide range of polymer blends.In this review,we mainly focus on the compatibilizing effects of Janus nanofillers of various morphologies,including spherical,snowman-like,and two-dimensional nanosheets,on polymer blends.We shed light on the impacts of compatibilization of Janus particles on phase morphologies,mechanical properties,and functionalities of polymer blends.This review could provide a guidance for designing an effective Janus particle compatibilizer to develop high-performance polymer blends.展开更多
基金supported by the Fundamental Research Funds for Central Universities(No.30922010811).
文摘It is important to understand the evolution of the matter on the polymer membrane surface.The in situ and real-time monitoring of the membrane surface will not only favor the investigation of selective layer formation but can also track the fouling process during operation.Herein,an aggregation-induced emission(AIE)-active polymer membrane was prepared by the interfacial polymerization of a cyclodextrin-based glycocluster(CD@Glucose)and a tetraphenylethylene derivative modified with boronic acid groups(TPEDB)on the surface of a polyacrylonitrile(PAN)ultrafiltration membrane.This interfacial polymerization method can be stacked layer-by-layer to regulate the hydrophilicity and pore structure of the membrane.With the increase in the number of polymer layers,the separation and antifouling properties of the membrane gradually improved.Owing to the AIE property of the crosslinking agent TPEDB,the occurrence of interfacial polymerization and the degree of fouling during membrane operation can be monitored by the fluorescence distribution and intensity.With the aggravation of membrane fouling,the fluorescence decreased gradually,but recovered after cleaning.Therefore,this AIE effect can be used for real-time monitoring of interfacial polymerization as well as membrane fouling.
文摘The preparation of composite charge-mosaic membrane included spinning of hollow fiber as the supporting membrane, preparing a selective layer on the inside surface of the fiber by interfacial polymerization. The charge-mosaic membranes show a high salt permeability while retaining sucrose. The charge-mosaic membrane can be effectively used to separate multivalent salts with organic matter of molecular weight great than 300 g/mol in industry.
基金financially supported by the National Natural Science Foundation of China(No.51903090)the Science and Technology Program of Guangzhou(No.202102020632)Fundamental Research Funds for the Central Universities(No.2020ZYGXZR046)。
文摘The high-efficiency fabrication of high-quality microcapsules containing epoxy is crucial to the further development of the potential practical self-healing epoxy systems based on microencapsulated two-part epoxy-amine chemistry.Herein,a novel microencapsulation technique based on non-equilibrium droplets via integrating electrospraying and interfacial polymerization(ES-IP)was established to efficiently microencapsulate epoxy monomers.The ES-IP technique,consisting of three continuous steps,i.e.electrospraying to massively generate droplets,enwrapping every single droplet through instant interfacial polymerization,and thickening shell at an elevated temperature,has great flexibility to regulate the microencapsulation process and the microcapsule quality.The fabricated core-shell structured epoxy microcapsules(Ep-MCs)were comprehensively characterized for their properties,showing that they have high cleanness with rare impurities,controllable and tunable size,good thermal stability and tightness,and high effective core fraction.The high-quality Ep-MCs were adopted to formulate a self-healing epoxy based on the microencapsulated epoxy-amine chemistry.The highest healing efficiency,in terms of the recovered mode I fracture toughness,of 110±17%was achieved after being healed at room temperature(~25℃)for 48 h.While the developed ES-IP technique facilitates the microencapsulation technique based on non-equilibrium droplets,the fabricated high-quality Ep-MCs greatly promote the further developments of the practical self-healing materials.
基金supported by the Open Project Program of State Key Laboratory of Petroleum Pollution Control(Grant No.PPC2017014)CNPC Research Institute of Safety and Environmental Technology。
文摘Polyamide(PA)-based thin-film composite membranes exhibit enormous potential in water purification,owing to their facile fabrication,decent performance and desirable stability.However,the thick PA active layer with high transport resistance from the conventional interfacial polymerization hampers their applications.The controllable fabrication of a thin PA active layer is essential for high separation efficiency but still challenging.Herein,a covalent organic framework TpPa-1 interlayer was firstly deposited on a polyethersulfone(PES)substrate to reduce the thickness of PA active layer in interfacial polymerization.The abundant pores of TpPa-1 increase the local concentration of amine monomers by adsorbing piperazine molecules,while hydrogen bonds between hydrophilic groups of TpPa-1 and piperazine molecules slow down their diffusion rate.Arising from those synergetic effects,the PA active layer is effectively reduced from 200 nm to 120 nm.By optimizing TpPa-1 interlayer and PA active layer,the water flux of resultant membranes can reach 171.35 L·m^-2·h^-1·MPa^-1,which increased by 125.4%compared with PA/PES membranes,while the rejection rates of sodium sulfate and dyes solution remained more than 90%and 99%,respectively.Our strategy may stimulate rational design of ultrathin PA-based nanofiltration membranes with high performances.
基金Supported by the National Research Council of Science&Technology(NST)grant by the Korea government(MSIP)(No.CRC-15-07-KIER)
文摘Carbon dioxide(CO_2) is greenhouse gas which originates primarily as a main combustion product of biogas and landfill gas. To separate this gas, an inside coated thin film composite(TFC) hollow fiber membrane was developed by interfacial polymerization between 1,3–cyclohexanebis–methylamine(CHMA) and trimesoyl chloride(TMC). ATR-FTIR, SEM and AFM were used to characterize the active thin layer formed inside the PSf hollow fiber. The separation behavior of the CHMA-TMC/PSf membrane was scrutinized by studying various effects like feed gas pressure and temperature. Furthermore, the influence of CHMA concentration and TMC concentration on membrane morphology and performance were investigated. As a result, it was found that mutually the CHMA concentration and TMC concentration play key roles in determining membrane morphology and performance. Moreover, the CHMA-TMC/PSf composite membrane showed good CO_2/CH_4 separation performance. For CO_2/CH_4 mixture gas(30/70 by volume) test, the membrane(PD1 prepared by CHMA 1.0% and TMC 0.5%) showed a CO_2 permeance of 25 GPU and the best CO_2/CH_4 selectivity of 28 at stage cut of 0.1. The high CO_2/CH_4 separation performance of CHMA-TMC/PSf thin film composite membrane was mostly accredited to the thin film thickness and the properties of binary amino groups.
基金Supported by the National Natural Science Foundation of China（21076176） the Research and Development Project of Tangshan（10140201C-3）+1 种基金 the Research and Development Project of Hebei Province（07275113） the Research Fund of Tangshan Normal College
文摘A new aromatic diamine,3,5-diaminobenzoylpiperazine （3,5-DABP）,was synthesized from 3,5-diaminobenzoic acid and 1-formyl piperazine.The structure of 3,5-DABP was identified by FT-IR spectra and 1H NMR spectra.With 3,5-DABP as aqueous monomer and trimesoyl chloride （TMC） as organic monomer,thin film composite （TFC） nanofiltration membranes were prepared by interfacial polymerization technology.The salt rejection order of these TFC membranes is Na2SO4MgSO4MgCl2NaCl.This sequence indicates that the membranes are negatively charged.
基金supported by the National Key Research&Development Program of China(2017YFB0603400)the National Natural Science Foundation of China(21938007)。
文摘Thin film composite(TFC)membranes with nanofillers additives for CO_(2)separation show promising applications in energy and environment-related fields.However,the poor compatibility between nanofillers and polymers in TFC membranes is the main problem.In this work,covalent organic frameworks(COFs,TpPa-1)with rich ANHA groups were incorporated into polyamide(PA)segment via in situ interfacial polymerization to prepare defect-free TFC membranes for CO_(2)/N_(2)separation.The formed covalent bonds between TpPa-1 and PA strengthen the interaction between nanofillers and polymers,thereby enhancing compatibility.Besides,the incorporated COFs disturb the rigid structure of the PA layer,and provide fast CO_(2)transfer channels.The incorporated COFs also increase the content of effective carriers,which enhances the CO_(2)facilitated transport.Consequently,in CO_(2)/N_(2)mixed gas separation test,the optimal TFC(TpPa_(0.025)-PIP-TMC/m PSf)membrane exhibits high CO_(2)permeance of 854 GPU and high CO_(2)/N_(2)selectivity of 148 at 0.15 MPa,CO_(2)permeance of 456 GPU(gas permeation unit)and CO_(2)/N_(2)selectivity of 92 at 0.5 MPa.In addition,the Tp Pa_(0.025)-PIP-TMC/m PSf membrane also achieves high permselectivty in CO_(2)/CH_(4)mixed gas separation test.Finally,the optimal TFC membrane showes good stability in the simulated flue gas test,revealing the application potential for CO_(2)capture from flue gas.
基金Sponsored by the National Natural Science Foundation of China (Grant No.50978068)International Cooperation Program (Grant No.2010DFA92460)+1 种基金the National High Technology Research and Development Program (863 Program,Grant No.2008AA06Z304)the Research Fund of Tianjin Key Laboratory of Aquatic Science and Technology
文摘A novel NF membrane prepared with poly（amidoamine） （PAMAM） dendrimer and trimesoyl chloride （TMC） by interfacial polymerization on polysulfone （PSF） ultrafiltration membrane was investigated. Field emission scanning electron microcopy （ FESEM）, atomic force micrograph （ AFM ） and contact angle （CA） of pure water on PA and PSF substrate were employed to characterize the chemical and physical properties of membranes. The PAMAM concentration, retention of salt solutions and organics were studied on the performance of the NF membrane. From the analyses of SEM and AFM, the polyamide active skin layers of the composite membranes are dense, rough, and finely dispersed nodular structures, packed tightly by the spherical globules. The contact angle of PA nanofitration membrane decreased after polymerization. The higher PAMAM concentra- tion can result in lower flux and higher rejection. The salt rejection of PA membranes decreases in the order K2 SO4 〉 Na2 SO4 〉 MgSQ 〉 MgC12 〉 CaC12 〉 NaC1, which indicates that the resulting membranes is nagatively charged. The pH increases from 3 to 10 in the feed resulting in the decrease of the flux and the increase of the rejection for NazSO4 solution. The molecular weight cut off （MWCO） of the composite NF membrane is nearly 860 kg/mol. The resulted PA membrane can be used to seoarate small organics and salt solutions.
基金Natural Science Foundation of Shanxi Province (20041029)Project of Science and Technology of Shanxi Province (012078)
文摘A polyurea-chlorocyclophosphazene microcapsule flame retardant is prepared by an interfacial polymerization process using 2,4-toluene diisocyanate (TDI) and hexanediamine as the raw materials. TG tests show that the thermal decomposition temperature of chlorocyclophosphazene in microcapsule obviously rises. The flame retardancy of HDPE/chlorocyclophosphazene in microencapsules is better than that of HDPE/chlorocyclophosphazene. Mechanical properties of HDPE/chlorocyclophosphazene microencapsule turn out to be superior to those of HDPE/chlorocyclophosphazene.
基金supported by Zhejiang Provincial Natural Science Foundation of China (LZ20B060001)National Natural Science Foundation of China (22008208&21908192)China Postdoctoral Science Foundation (2019TQ0276)。
文摘Enhancing the water permeation while maintaining high salt rejection of existing reverse osmosis(RO)membranes remains a considerable challenge.Herein,we proposed to introduce polymer of intrinsic microporosity,PIM-1,into the selective layer of reverse osmosis membranes to break the trade-off effect between permeability and selectivity.A water-soluble a-LPIM-1 of low-molecular-weight and hydroxyl terminals was synthesized.These designed characteristics endowed it with high solubility and reactivity.Then it was mixed with m-phenylenediamine and together served as aqueous monomer to react with organic monomer of trimesoyl chloride via interfacial polymerization.The characterization results exhibited that more“nodule”rather than“leaf”structure formed on RO membrane surface,which indicated that the introduction of the high free-volume of a-LPIM-1 with three dimensional twisted and folded structure into the selective layer effectively caused the frustrated packing between polymer chains.In virtue of this effect,even with reduced surface roughness and unchanged layer thickness,the water permeability of prepared reverse osmosis membranes increased 2.1 times to 62.8 L·m^(-2)·h^(-1) with acceptable Na Cl rejection of 97.6%.This attempt developed a new strategy to break the trade-off effect faced by traditional polyamide reverse osmosis membranes.
文摘Although a great progress has been achieved for the development of NF membranes and technologies and SRNF do show a great potential in the separation of organic components, an NF membrane with good separation performance and good resistance to organic solvents are urgently needed for a more complicated situation in practical. In this study, a kind of solvent-resistant nanofiltration (SRNF) membrane was fabricated via interfacial polymerization on a laboratory optimized cellulose acetate (CA) basic membrane. The effects of interfacial polymerization parameters, such as water phase concentration, immersed time in the water phase and in the organic phase, on the pure water flux and rejection rate of C-2R yellow dyestuffs were investigated. A highest dye rejection rate of 72.9% could be obtained by water phase solution containing 1% m-xylylenediamine (mXDA) and organic phase solution with 0.2% trimesoyl chloride (TMC) under immersed time in water phase of 6 minutes and in organic phase of 40 seconds. This membrane demonstrated better resistance to methyl alcohol compared to commercial membrane. This study may offer an avenue to develop a solvent-resistant nanofiltration membrane.
文摘The surface and interfacial properties of polymeric bonding agents and nitramine crystal fillers were studied. The surface free energy and adhesion work of polymeric bonding agents and nitramine fillers were calculated by using Kaeble′s equations. It was observed that the hydroxyl values of neutral polymeric bonding agents (NPBA) correlate well with the polar components of surface free energies. On the basis of the measurements of swelling ratio and initial modulus, the interfacial bonding through highly crosslinked polymeric shell formation around the nitramine particles and generating interfacial reinforcement were rationalized. The application of Tapping Mode AFM (atomic force micro scope) to observing the surface morphology of NPBA reveals that methyl acrylate monomer appears to play a role for aiding the formation of network like structure when nanometer scale images of NPBA are created.
基金National Natural Science Foundation of China(51773169 and 51973173)Guangdong Basic and Applied Basic Research Foundation(2019B1515120093)+2 种基金Technological Base Scientific Research ProjectsNatural Science Basic Research Plan for Distinguished Young Scholars in Shaanxi Province(2019JC-11)Polymer Electromagnetic Functional Materials Innovation Team of Shaanxi Sanqin Scholars.
文摘Rapid development of energy,electrical and electronic technologies has put forward higher requirements for the thermal conductivities of polymers and their composites.However,the thermal conductivity coefficient(λ)values of prepared thermally conductive polymer composites are still difficult to achieve expectations,which has become the bottleneck in the fields of thermally conductive polymer composites.Aimed at that,based on the accumulation of the previous research works by related researchers and our research group,this paper proposes three possible directions for breaking through the bottlenecks:(1)preparing and synthesizing intrinsically thermally conductive polymers,(2)reducing the interfacial thermal resistance in thermally conductive polymer composites,and(3)establishing suitable thermal conduction models and studying inner thermal conduction mechanism to guide experimental optimization.Also,the future development trends of the three above-mentioned directions are foreseen,hoping to provide certain basis and guidance for the preparation,researches and development of thermally conductive polymers and their composites.
基金support and funding from National Scientific Research ProjectSpace Supporting Fund from China Aerospace Science and Industry Corporation(2019-HT-XG)+1 种基金Fundamental Research Funds for the Central Universities(310201911qd003)China Postdoctoral Science Foundation(2019M653735)。
文摘Poly(p-phenylene-2,6-benzobisoxazole)(PBO)fibers possess excellent dielectric,mechanical properties and heat resistance.However,the surface of PBO fibers is smooth and highly chemical inert,resulting in poor interfacial compatibility to polymer matrix,which severely limits its wider application in high-performance fiber-reinforced resin matrix composites.In this work,random copolymers(P(S-co-BCB-co-MMA))containing benzocyclobutene in the side-chain were synthesized by reversible addition-fragmentation chain transfer(RAFT)polymerization,which were then utilized to form dense random copolymer membrane on the surface of PBO fibers by thermally cross-linking at 250°C(PBO@P fibers).Four kinds of synthesized P(S-co-BCB-co-MMA)with different number-average molar mass(Mn)were well controlled and possessed narrow dispersity.When the Mnwas 32300,the surface roughness of PBO@P fibers was increased from 11 nm(PBO fibers)to 39 nm.In addition,PBO@P fibers presented the optimal interfacial compatibility with bisphenol A cyanate(BADCy)resins.And the single fiber pull-out strength of PBO@P fibers/BADCy micro-composites was 4.5 MPa,increasing by 45.2%in comparison with that of PBO fibers/BADCy micro-composites(3.1 MPa).Meantime,PBO@P fibers still retained excellent tensile strength(about 5.1 GPa).Overall,this work illustrates a simple and efficient surface functionalization method,which would provide a strong theoretical basis and technical support for controlling the surface structure&chemistry of inert substrates.
基金Project(2008AA03Z207) supported by the National Hi-tech Research and Development Program of China
文摘H+ doped polyaniline nanofibre(PH) was synthesized by interfacial polymerization and polyanilines doped with Li salt(PLI and PHLI) were prepared by immersing emeraldine base(EB) and H+ doped polyaniline in 1 mol/L LiPF6/(EC-EMC-DMC),respectively.PH,PLI and PHLI were all characterized by scanning electron microscopy(SEM) and Fourier transform infrared(FT-IR) spectrometry.With 1 mol/L LiPF6/(EC-EMC-DMC) as electrolyte,PH,PHLI and PLI were used as the active materials of symmetric non-aqueous redox supercapacitors.PLI shows the highest initial specific capacitance of 120 F/g(47 F/g for PH and 66 F/g for PHLI) among three samples.After 500 cycles,the specific capacitance of PLI remains 75 F/g,indicating the good cycleability.
基金supported by the Science Challenge Project(No.TZ2018004)the Fundamental Research Funds for the Central Universities(No.2232019D3-10)+1 种基金the National Natural Science Foundation of China(Nos.51473168,21674113,21334007,21790340)the Programs of Chinese Academy of Sciences(Nos.QYZDY-SSW-SLH027,YJKYYQ20190084).
文摘The stability of ultrathin polymer films plays a crucial role in their technological applications.Here,we systematically investigated the influence of interfacial adsorption in physical aging and the stability of thin polymer films in the solvent-induced process.We further identify the stability mechanism from the theory of thin film stability.Our results show that the aging temperature and film thickness can strongly influence the stability of thin PS films in acetone vapor.Physical aging can greatly improve the stability of thin polymer films when the aging temperature T_(aging1)>T_(g).A thinner PS film more quickly reaches a stable state via physical aging.At short aging time,the formation of the adsorbed layer can reduce the polar interaction;however,it slightly influences the stability of thin polymer films in the solvent-induced process.At later aging stage,the conformational rearrangement of the polymer chains induced by the interfacial effect at the aging temperature Taging1 plays an important role in stabilizing the thin polymer films.However,at T_(aging2)<T_(g),the process of physical aging slightly influences the stability of the thin polymer films.The formation of the adsorbed layer at Taging2 can reduce the short-range polar interaction of the thin film system and cannot suppress the instability of thin polymer films in the solvent-induced process.These results provide further insight into the stable mechanism of thin polymer films in the solvent-induced process.
基金The authors thank the National Natural Science Foundation of China(No.51973193)the State Key Laboratory of Chemical Engineering(No.SKL-ChE-13D)for their financial support.
文摘Immiscible polymer blends are an important family of polymer materials.The interfacial thickness between different phases is a very important parameter that dictates,to a great extent,the morphology and properties of such a blend.This work explores and optimizes an up-to-date atomic force microscopy(AFM)of type NanoIR2^(TM) system in order to quantitatively measure the interfacial thickness of immiscible polymer blends.This system is equipped with two nano-probes capable of detecting the response of a material to an infrared pulse called AFM-infrared spectroscopy mode(AFM-IR)or conducting resonance called AFM-Lorentz Contact Resonance mode(AFM-LCR),respectively.Its potential for quantitatively measuring the interfacial thickness of immiscible polymer blends is evaluated using blends composed of polyamide 6(PA6)and polyolefin elastomer(POE)in the presence or absence of a POE containing maleic anhydride(POE-g-MAH)as a compatibilizer.Surface roughness affects adversely the signal intensity and consequently an accurate measurement of the interfacial thickness.Optimum sample surface preparation procedures are proposed.
基金Financial supports from the National Natural Science Foundation of China (51575030, 51532002 and 51872027)Beijing Natural Science Foundation (L172023)National Basic Research Program of China (2017YFE0113500)。
文摘The solid-state lithium battery is considered as an ideal next-generation energy storage device owing to its high safety,high energy density and low cost.However,the poor ionic conductivity of solid electrolyte and low interfacial stability has hindered the application of solid-state lithium battery.Here,a flexible polymer/garnet solid electrolyte is prepared with poly(ethylene oxide),poly(vinylidene fluoride),Li6.75La3 Zr1.75Ta0.25O12,lithium bis(trifluoromethanesulfonyl)imide and oxalate,which exhibits an ionic conductivity of 2.0 ×10^(-4) S cm^(-1) at 55℃,improved mechanical property,wide electrochemical window(4.8 V vs.Li/Li+),enhanced thermal stabilities.Tiny acidic OX was introduced to inhibit the alkalinity reactions between Li6.75La3 Zr1.75Ta0.25O12 and poly(vinylidene fluoride).In order to improve the interfacial stability between cathode and electrolyte,an Al2 O3@LiNi0.5Co0.2Mn0.3O2 based composite cathode framework is also fabricated with poly(ethylene oxide) polymer and lithium salt as additives.The solid-state lithium battery assembled with polymer/garnet solid electrolyte and composite cathode framework demonstrates a high initial discharge capacity of 150.6 mAh g^(-1) and good capacity retention of 86.7% after 80 cycles at 0.2 C and 55℃,which provides a promising choice for achieving the stable electrode/electrolyte interfacial contact in solid-state lithium batteries.
基金the support for this work by National Natural Science Foundation of China(Grant Nos.22175139 and 22105156)。
文摘The weak interface interaction and solid-solid phase transition have long been a conundrum for 1,3,5,7-tetranitro-1,3,5,7-tetraazacyclooctane(HMX)-based polymer-bonded explosives(PBX).A two-step strategy that involves the pretreatment of HMX to endow—OH groups on the surface via polyalcohol bonding agent modification and in situ coating with nitrate ester-containing polymer,was proposed to address the problem.Two types of energetic polyether—glycidyl azide polymer(GAP)and nitrate modified GAP(GNP)were grafted onto HMX crystal based on isocyanate addition reaction bridged through neutral polymeric bonding agent(NPBA)layer.The morphology and structure of the HMX-based composites were characterized in detail and the core-shell structure was validated.The grafted polymers obviously enhanced the adhesion force between HMX crystals and fluoropolymer(F2314)binder.Due to the interfacial reinforcement among the components,the two HMX-based composites exhibited a remarkable increment of phase transition peak temperature by 10.2°C and 19.6°C with no more than 1.5%shell content,respectively.Furthermore,the impact and friction sensitivity of the composites decreased significantly as a result of the barrier produced by the grafted polymers.These findings will enhance the future prospects for the interface design of energetic composites aiming to solve the weak interface and safety concerns.
基金the National Natural Science Foundation of China (Nos. 52173076 and 52042302)China Postdoctoral Science Foundation (No. 2021M701825)+1 种基金Tsinghua-Foshan Innovation Special Fund (TFISF) (No. 2021THFS0212)Joint Agency Affiliate Projects of China Petroleum & Chemical Corporation (No. 20212930037)。
文摘Mixing two or more polymers to produce the“polymer alloy”is one of the most versatile and economical strategies for developing new polymeric materials.The compatibility between polymer components largely determines the comprehensive performance of polymer blend.More recently,a type of unique surface partitioned materials,Janus particles,has been proposed to act as a novel interfacial compatibilizer for polymer blends.Such Janus particles integrates the amphipathicity of diblock copolymer and interfacial stabilization of nanoparticles,displaying a significant superiority in comparison with molecular compatibilizers for a wide range of polymer blends.In this review,we mainly focus on the compatibilizing effects of Janus nanofillers of various morphologies,including spherical,snowman-like,and two-dimensional nanosheets,on polymer blends.We shed light on the impacts of compatibilization of Janus particles on phase morphologies,mechanical properties,and functionalities of polymer blends.This review could provide a guidance for designing an effective Janus particle compatibilizer to develop high-performance polymer blends.
