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High-performance and robust high-temperature polymer electrolyte membranes with moderate microphase separation by implementation of terphenyl-based polymers
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作者 Jinyuan Li Congrong Yang +3 位作者 Haojiang Lin Jicai Huang Suli Wang Gongquan Sun 《Journal of Energy Chemistry》 SCIE EI CAS CSCD 2024年第5期572-578,共7页
Acid loss and plasticization of phosphoric acid(PA)-doped high-temperature polymer electrolyte membranes(HT-PEMs)are critical limitations to their practical application in fuel cells.To overcome these barriers,poly(te... Acid loss and plasticization of phosphoric acid(PA)-doped high-temperature polymer electrolyte membranes(HT-PEMs)are critical limitations to their practical application in fuel cells.To overcome these barriers,poly(terphenyl piperidinium)s constructed from the m-and p-isomers of terphenyl were synthesized to regulate the microstructure of the membrane.Highly rigid p-terphenyl units prompt the formation of moderate PA aggregates,where the ion-pair interaction between piperidinium and biphosphate is reinforced,leading to a reduction in the plasticizing effect.As a result,there are trade-offs between the proton conductivity,mechanical strength,and PA retention of the membranes with varied m/p-isomer ratios.The designed PA-doped PTP-20m membrane exhibits superior ionic conductivity,good mechanical strength,and excellent PA retention over a wide range of temperature(80–160°C)as well as satisfactory resistance to harsh accelerated aging tests.As a result,the membrane presents a desirable combination of performance(1.462 W cm^(-2) under the H_(2)/O_(2)condition,which is 1.5 times higher than that of PBI-based membrane)and durability(300 h at 160°C and 0.2 A cm^(-2))in the fuel cell.The results of this study provide new insights that will guide molecular design from the perspective of microstructure to improve the performance and robustness of HT-PEMs. 展开更多
关键词 Fuel cell High-temperature polymer electrolyte membranes microphase separation Poly(terphenyl piperidinium)s Phosphoric acid
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SYNTHESIS AND CHARACTERIZATION OF AMPHIPHILIC GRAFT COPOLYMER CONTAINING MICROPHASE SEPARATED AND LONG POLY(ETHYLENE OXIDE) SIDE CHAIN STRUCTURES 被引量:4
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作者 邱永兴 俞小洁 +1 位作者 封麟先 杨士林 《Chinese Journal of Polymer Science》 SCIE CAS CSCD 1993年第1期67-75,共9页
Acryloyl terminated Poly (ethyleneoxide)macromonomers (PEO-A) with different PEO chain lengths have been prepared by deactivation of PEO alkoxide with acryloyl chloride. A new kind of amphiphilic polystyrene-g-poly (e... Acryloyl terminated Poly (ethyleneoxide)macromonomers (PEO-A) with different PEO chain lengths have been prepared by deactivation of PEO alkoxide with acryloyl chloride. A new kind of amphiphilic polystyrene-g-poly (ethylene oxide)graft copolymer containing both microphase separated and PEO side chain structures has been synthesized from radical copolymerization of PEO-A macromonomer with styrene. After careful purification by a newly-developed method called 'selective dissolution', the well-defined structure of the purified copolymers was confirmed by IR, ~1H-NMR and GPC. Various experimental parameters controlling the copolymerization were studied in detail. The results indicated that the feed ratio of styrene to macromonomer(S/M) was the most important determining factor for the composition of the copolymers. A detailed 'comb- model' was proposed to describe the molecular structure of the graft copolymers. Finally, this amphiphilic graft copolymers may readily form microphase separated structures as clearly indicated by transmission electron microscopy. 展开更多
关键词 PEO AIBN SIDE CHAIN STRUCTURES SYNTHESIS AND CHARACTERIZATION OF AMPHIPHILIC GRAFT COPOLYMER CONTAINING microphase SEPARATED AND LONG POLY ETHYLENE OXIDE PS
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MICROPHASE SEPARATED STRUCTURES AND PROPERTIES OF PDMS-MDIPEG COPOLYMER SURFACE 被引量:1
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作者 方红霞 《Chinese Journal of Polymer Science》 SCIE CAS CSCD 2009年第3期327-334,共8页
A series of poly(dimethylsiloxane)(PDMS)-4,4′-diphenylmethanediisocyanate(MDI)-poly(ethylene glycol)(PEG) multiblock copolymers were synthesized by employing two-step growth polymerization and investigated by AFM,XPS... A series of poly(dimethylsiloxane)(PDMS)-4,4′-diphenylmethanediisocyanate(MDI)-poly(ethylene glycol)(PEG) multiblock copolymers were synthesized by employing two-step growth polymerization and investigated by AFM,XPS. contact angle system,protein adsorption and platelets adhesion measurements,respectively.It was found that as the molecular weight of PDMS increased,the surface of copolymers had increasing phase separation,while the increase in the molecular weight of PEG decreased the phase separation extents of the copolymer surface.XPS and contact angle measurements showed that the greater the phase separation extent was,the lower both the surface enrichment of PDMS and the surface free energy of the copolymer film were.The protein adsorption experiments indicated that the best phase separation did not exhibit the best biocompatibility. 展开更多
关键词 microphase separated structure Multiblock copolymer PDMS-PEG-MDI Protein adsorption
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ORDERED STRUCTURAL EVOLUTION AND RELAXATION BEHAVIORS OF A SERIES MICROPHASE SEPARATED“HAIRY-ROD”POLYIMIDES WITH MULTIPLE ALKYL SIDE CHAINS
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作者 Zhi-haoShen AlexanderJ.Jing +3 位作者 ShiJin Hua-binWang FrankW.Hams StephenZ.D.Cheng 《Chinese Journal of Polymer Science》 SCIE CAS CSCD 2005年第2期171-186,共16页
A series of“hairy-rod”polyimides,BBPA(n),with multiple alkyl side chains was prepared from 3,3',4,4'-biphenyltetracarboxylic dianhydride(BPDA)and 4,4'-biphenyldiamine substituted in the 2,2'-position... A series of“hairy-rod”polyimides,BBPA(n),with multiple alkyl side chains was prepared from 3,3',4,4'-biphenyltetracarboxylic dianhydride(BPDA)and 4,4'-biphenyldiamine substituted in the 2,2'-positions with benzoate,whichwas substituted in the 3,4,5-positions with ether side chains of varying lengths.The number of the methylene units,n,inthese alkyl side chains were in even numbers ranging from 8 to 18.Combining techniques of one-dimensional(1D)and 2Dwide angle x-ray diffraction,1D small angle X-ray scattering,differential scanning calorimetry experiments,it was found thatthis series of“hairy-rod”polyimides possess a micro-phase separation between the backbones and side chains.This led to theformation of ordered structures in two different length scales,of which both are hexagonal packing:one is attributed to thealkyl side chains on the sub-nanometer scale,and another is for the whole polymer chains on the nanometer scale.Thedevelopment of the hexagonal structure on the sub-nanometer scale was critically dependent upon the lengths of the alkylside chains.Three relaxation processes were captured by dynamic mechanical analysis,i.e.,segmental motion of thebackbones,α,the melting of the side chain crystals,β_1,which exits only for the materials with longer side chains(n=18,16);and the subglass relaxation of side chains,β_2.The peak relaxation temperature of the α process decreased withincreasing the length of side chains,while the one of the β_2 process increased.The activation energy of the α relaxation wasrelatively independent on the length of side chain,whereas,β_2 process showed the increasing of activation energy withincreasing the length of side chains. 展开更多
关键词 Polyimides Hairy-rod microphase separation.
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Synthesis, Purification and Characterization of Amphiphilic and Microphase Separated Graft Copolymer Polystyrene-g-Poly(ethylene oxide)
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作者 QIU Yong-xing, YU Xiao-jie, FENG Lin-xian and YANG Shi-lin (Department of Polymer Science and Engineering, ZheJiang University, Hangzhou) 《Chemical Research in Chinese Universities》 SCIE CAS CSCD 1992年第3期278-286,共9页
The present paper covers the poly (ethylene oxide) macromer with vinyl benzyl terminal group (PEO-VB) prepared by deactivation of the alkoxide function of mono-functional 'living' PEO chains with vinyl benzyl ... The present paper covers the poly (ethylene oxide) macromer with vinyl benzyl terminal group (PEO-VB) prepared by deactivation of the alkoxide function of mono-functional 'living' PEO chains with vinyl benzyl chloride (VBC). The obtained macromers were subjected to careful purification and detailed characterization. A new kind of amphiphilic polystyrene-g-poly(ethylene oxide) (PS-g-PEO) with both mi-crophase separated and PEO side chains was synthesized from radical copolymerization of PEO-VB macromer with styrene monomer. An improved purification method, referred as 'selective dissolvation', was established for the isolation of graft copolymers from the grafting products, and the purity and yield of the purified copolymers were satisfactory. The well-defined structure of the purified copolymers was confirmed by IR, 1H NMR and GPC. The bulk composition of the graft copolymers was determined by a well-established first derivative UV spectrometry. Various experimental parameters controlling the copolymerization were also studied. The results indicate that the feed ratio of macromer to styrene (M/S) was the most important factor in determining the composition of the copolymers. Thus a series of PS-g-PEO with a wide range of bulk compositions were obtained simply by adjusting the value of M/S. As clearly indicated by transmission electron microscopy, this amphiphilic graft copolymers may readily form microphase separated structures. 展开更多
关键词 Poly(ethyiene oxide) macromer Polystyrene-g-poly(ethylene oxide) Pu-rification of graft copolymer Amphiphilic and microphase separated structure Biocom-patible polymer
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Reservoir Characteristics and Main Controlling Factors of the Flow III Section of the K Oilfield in the Weixinan Depression
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作者 Shijin Tan 《Open Journal of Yangtze Oil and Gas》 2024年第2期33-47,共15页
In order to clarify the reservoir characteristics and main controlling factors of the flow three section of the K oil field in the Weixinan Depression, a study on the reservoir characteristics and main controlling fac... In order to clarify the reservoir characteristics and main controlling factors of the flow three section of the K oil field in the Weixinan Depression, a study on the reservoir characteristics and main controlling factors of the flow three section of the K oil field in the Weixinan Depression has been carried out by utilizing the data of cores, casting thin sections, physical property tests and logging wells. The results show that the lithology of the reservoir in the flow three section of the study area is dominated by coarse sandstone and medium sandstone, followed by conglomerate-bearing sandstone and sand conglomerate. The porosity is mainly distributed in the range of medium-high porosity, and the permeability is mainly medium seepage, and the overall physical properties are good. The three sections of the stream in the study area mainly include four sedimentary microphases, namely, underwater diversion channel, estuarine dam, mat sand and inter-diversion bay. The underwater diversion channel has the best physical properties, characterized by coarse grains and low mud content. The medium and coarse sand content of various lithologic reservoirs is the main factor in the formation of high-quality reservoirs. Rock-forming action is an important factor affecting the physical properties of local reservoirs, comparing the compaction, cementation and dissolution between different sedimentary microphases, the underwater diverging river has the lowest rate of compaction and pore reduction, the highest rate of pore increase by dissolution, and the best physical properties. Therefore, the weakly cemented-strongly dissolved coarse sandstone phase developed in the microphase of the underwater diversion channel in section 3 of the flow in the study area is the most favorable reservoir. 展开更多
关键词 Weinan Depression Liushagang Formation Reservoir Characteristics Sedimentary microphase DIAGENESIS
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Polymerization-induced microphase separation of polymer-polyoxometalate nanocomposites for anhydrous solid state electrolytes 被引量:1
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作者 Lu Liu Zicheng Wu +3 位作者 Zhao Zheng Qianjie Zhou Kun Chen Panchao Yin 《Chinese Chemical Letters》 SCIE CAS CSCD 2022年第9期4326-4330,共5页
Solid-state electrolytes(SSEs)with high ionic conductivity,mechanical stability,and high thermal stability,as well as the stringent requirement of application in high-temperature fuel cells and lithium-ion batteries i... Solid-state electrolytes(SSEs)with high ionic conductivity,mechanical stability,and high thermal stability,as well as the stringent requirement of application in high-temperature fuel cells and lithium-ion batteries is receiving increasing attention.Polymer nanocomposites(PNCs),combining the advantages of inorganic materials with those of polymeric materials,offer numerous opportunities for SSEs design.In this work,we report a facile and general one-pot approach based on polymerization-induced microphase separation(PIMS)to generate PNCs with bi-continuous microphases.This synthetic strategy transforms a homogeneous liquid precursor consisting of polyoxometalates(POMs,H_(3)PW_(12)O_(40),Li_(7)[V_(15)O_(36)(CO_(3))]),poly(ethylene glycol)(PEG)macro-chain-transfer agent,styrene and divinylbenzene monomers,into a robust and transparent monolith.The resulting POMs are uniformly dispersed in the PEG block(PEG/POM)to form a conducting pathway that successfully realizes the effective transfer of protons and lithium ions,while the highly cross-linked polystyrene domains(P(S-co-DVB))as mechanical support provide outstanding mechanical properties and thermal stability.As the POM loading ratio up to 35 wt%,the proton conductivity of nanocomposite reaches as high as 5.99×10^(-4) S/cm at 100℃ in anhydrous environment,which effectively promotes proton transfer under extreme environments.This study broadens the application of fuel cells and lithium-ion batteries in extreme environments. 展开更多
关键词 Solid-state electrolyte microphase separation Bi-continuous structure POLYMER POLYOXOMETALATE
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EFFECT OF MOLECULAR WEIGHT AND FILM THICKNESS ON THE CRYSTALLIZATION AND MICROPHASE SEPARATION IN POLYSTYRENE-BLOCK-POLY(L-LACTIC ACID) THIN FILMS AT THE EARLY STAGE
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作者 于新红 《Chinese Journal of Polymer Science》 SCIE CAS CSCD 2011年第3期325-335,共11页
We investigated the effects of molecular weight and film thickness on the crystallization and microphase separation in semicrystalline block copolymer polystyrene-block-poly(L-lactic acid) (PS-b-PLLA) thin films, ... We investigated the effects of molecular weight and film thickness on the crystallization and microphase separation in semicrystalline block copolymer polystyrene-block-poly(L-lactic acid) (PS-b-PLLA) thin films, at the early stage of film evolution (when Tg 〈 T 〈 TODT) by in situ hot stage atomic force microscopy. For PS-b-PLLA 1 copolymer which had lower molecular weight and higher PLLA fraction, diffusion-controlled break-out crystallization started easily. For PS-b-PLLA 2 with higher molecular weight, crystallization in nanometer scales occurs in local area. After melting of the two copolymer films, islands were observed at the film surface: PS-b-PLLA 1 film was in a disordered phase mixed state while PS-b-PLLA 2 film formed phase-separated lamellar structure paralleling to the substrate. Crystallization-melting and van der Waals forces drove the island formation in PS-b-PLLA 1 film. Film thickness affected the crystallization rate. Crystals grew very slowly in much thinner film of PS-b-PLLA 1 and remained almost unchanged at long time annealing. The incompatibility between PS and PLLA blocks drove the film fluctuation which subsequently evolved into spinodal-like morphology. 展开更多
关键词 CRYSTALLIZATION microphase separation Molecular weight Film thickness Early stage.
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Synthesis and Microphase Separation Behavior of Random, Mixed Cylindrical Brush Copolymers Bearing Polystyrene and Poly(ε-caprolactone) Side Chains
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作者 Houluo Cong Sen Xu 郑思珣 《Chinese Journal of Polymer Science》 SCIE CAS CSCD 2017年第12期1572-1586,共15页
A series of mixed, random cylindrical brush copolymers bearing polystyrene(PS) and poly(ε-caprolactone)(PCL) side chains were synthesized via the combination of ring-opening polymerization(ROP) and atom trans... A series of mixed, random cylindrical brush copolymers bearing polystyrene(PS) and poly(ε-caprolactone)(PCL) side chains were synthesized via the combination of ring-opening polymerization(ROP) and atom transfer radical polymerization(ATRP). These novel cylindrical brush copolymers have been characterized by means of nuclear magnetic resonance(NMR) spectroscopy, gel permeation chromatography(GPC) and differential scanning calorimetry(DSC). It was found that the mikto-armed cylindrical brush copolymers were microphase-separated in bulks and that the morphologies were dependent on the mass ratios of PS to PCL side chains. One of the cylindrical brush copolymers was employed to incorporate into epoxy thermoset to investigate effect of the mikto-armed cylindrical brush architecture on the reaction-induced microphase separation behavior. Depending on the concentration of the cylindrical brush in epoxy, the thermosets can display the morphologies with the spherical, worm-like and lamellar PS microdomains dispersing in continuous thermosetting matrices. 展开更多
关键词 Cylindrical brush copolymers Block copolyrner EPOXY Reaction-induced microphase separation
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Flexible coatings with microphase separation structure attained by copolymers and ultra-fine nanoparticles for endurable antifouling
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作者 Zhuo Chen Shun Chen +3 位作者 Yufei Xiong Yuping Yang Yang Zhang Lijie Dong 《Journal of Materials Science & Technology》 SCIE EI CAS CSCD 2021年第23期179-186,共8页
Incorporating antibacterial agent into biomimetic coating inspired by natural organisms with micronano structure surface has generated more interest for antifouling applications.In this work,poly(dimethylsiloxane)(PDM... Incorporating antibacterial agent into biomimetic coating inspired by natural organisms with micronano structure surface has generated more interest for antifouling applications.In this work,poly(dimethylsiloxane)(PDMS)-based triblock copolymers and sub-20 nm nanoparticles Ag and heterogeneous Fe_(3)O_(4)-coated Ag(Fe_(3)O_(4)@Ag)were used to construct microphase separation topography with oriented copolymer blocks structure.The artificial surface was verified by atomic force microscopy and scanning electron microscopy images.Meanwhile,the surface exhibited relative stable hydrophobic property,which was demonstrated by the water contact angle and dynamic air-bubble contact angle measurements.Consequently,after immersed in BSA solution 24 h and 720 h,the actual BSA absorption amount of the surface with Fe_(3)O_(4)@Ag nanoparticles was as low as 10%and 27%that of the initial BSA amount,respectively.Moreover,the surface also showed remarkable antibacterial performance,which effectively suppressed the growth rate of Escherichia coli.The strategy of constructing the flexible micro p hase separation structure by introducing heterogeneous inorganic antibacterial nanoparticles into a block copolymer substrate opens up a new way to create an antifouling surface coating. 展开更多
关键词 microphase separation topography Ultra-fine nanoparticles Antifouling surfaces Antibacterial performance
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Influence of Diisocyanate on Polyurethane Elastomers Which Crosslinked by β-Cyclodextrin 被引量:2
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作者 An Xie Ming Zhang Shin-Ichi Inoue 《Open Journal of Organic Polymer Materials》 CAS 2016年第3期99-111,共13页
A series of polyurethane elastomers (PUEs) were synthesized by using β-cyclodextrin (β-CD) as cross-linker from aliphatic, alicyclic, aromatic diisocyanates, and polyol. The PUEs were characterized by Fourier Transf... A series of polyurethane elastomers (PUEs) were synthesized by using β-cyclodextrin (β-CD) as cross-linker from aliphatic, alicyclic, aromatic diisocyanates, and polyol. The PUEs were characterized by Fourier Transform Infrared Spectroscopy (FTIR), Scanning Electron Microscopy (SEM), Differential Scanning Calorimetry (DSC), Dynamic Mechanical Analysis (DMA), swelling test, hardness test and tensile test. The influence of diisocyanate on microphase separation and properties of PUEs was evaluated. 展开更多
关键词 CYCLODEXTRIN Polyurethane Elastomer microphase Separation CROSS-LINKER
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Nanoindentation Measurements of Mechanical Properties of Polyurethane Elastomers Which Crosslinked by β-Cyclodextrin 被引量:1
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作者 An Xie Xiaoyuan Ji +2 位作者 Yingjie Chen Ming Zhang Shin-Ichi Inoue 《Open Journal of Organic Polymer Materials》 CAS 2016年第3期112-118,共7页
A series of PUEs which use β-CD as cross-linker were synthesized. Nanoindentation measurements of mechanical properties of these PUEs were made. Load and depth sensing indentation and nano DMA mode were used to evalu... A series of PUEs which use β-CD as cross-linker were synthesized. Nanoindentation measurements of mechanical properties of these PUEs were made. Load and depth sensing indentation and nano DMA mode were used to evaluate mechanical properties of PUEs in nano-scale. The difference between the results from two modes proved the microphase separation in PUEs and to investigate PUE from hard domains and soft domains was of great significance. 展开更多
关键词 Polyurethane Elastomer microphase Separation Load and Depth Sensing Indentation Nano DMA
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THE VISCOELASTIC EFFECT ON THE FORMATION OF MESO-GLOBULAR PHASE OF DILUTE HETEROPOLYMER SOLUTIONS
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作者 Chi Wu The Open Laboratory of Bond Selective Chemistry Department of Chemical Physics, University of Science and Technology of China, Hefei 230026 China Department of Chemistry The Chinese University of Hong Kong Shatin, Hong Kong 《Chinese Journal of Polymer Science》 SCIE CAS CSCD 2003年第2期117-122,共6页
Linear homopolymer chains in poor solvent exist either as individual crumpled single chain globules or asmacroscopic precipitate, depending on whether the solution is in the one- or the two-phase region. However, line... Linear homopolymer chains in poor solvent exist either as individual crumpled single chain globules or asmacroscopic precipitate, depending on whether the solution is in the one- or the two-phase region. However, linearheteropolymer chains in dilute solution might be able to form stable mesoglobules made up of a limited number of chains ifthe degree of amphiphilicity of the chain is sufficiently high and the experimental conditions are appropriate. The self-assembly of block copolymers in a selective solvent is typical of such examples. In practice, the formation of stablemesoglobules can be directly related to the formation of novel polymeric nanopaticles in solution. In this article, we willaddress the formaton of mesoglobular phase not only on the basis of thermodynamics, but also from a kinetic point of view,which leads to the discussion of how viscoelasticity can affect the phase behavior of heteropolymer chains in dilute solution.The formation and stabilization of several different kinds of novel polymeric nanopedicles will be used to illustrate ourdiscussion. 展开更多
关键词 VISCOELASTICITY Mesoglobular phase Heteropolymer NANOPARTICLE Polymer Dispersion microphase inversion
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The Effect of Interfacial Interactions on a Structure and Properties of Polyurethane Elastomer/Poly(Vinyl Chloride) Blends
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作者 T. L. Malysheva S. V. Golovan D. L. Starokadomsky 《Open Journal of Organic Polymer Materials》 2011年第1期1-7,共7页
The effect of chemical structure of segmented poly(urethane-urea)s on its interfacial interactions with poly(vinyl chloride) as well as supramolecular structure and the properties of prepared composites has been studi... The effect of chemical structure of segmented poly(urethane-urea)s on its interfacial interactions with poly(vinyl chloride) as well as supramolecular structure and the properties of prepared composites has been studied. A direct influence of flexible and rigid segments of elastomers on a compatibility, structure and the physical-mechanical properties of poly(urethane-urea)/poly(vinyl chloride) blends was investigated. A formation of intermolecular hydrogen bonds network in the poly(urethane-urea)/poly(vinyl chloride) systems was evaluated by FTIR analysis. Morphology studies have shown the effect of interfacial interactions on a size of thermoplastic phase dispersed within elastomer matrix. Obtained poly(urethane-urea)/poly(vinyl chloride) micro- and nanocomposites have improved tensile properties. 展开更多
关键词 Polymer Composites Compatibility microphase Separation Glass Transition Hard Domains CRYSTALLITES ASSOCIATES H-BONDS Urethane-Urea Groups Interfacial Interactions
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SYNTHESIS AND FINE STRUCTURE-PROPERTY RELATIONSHIPS OF ION-CONTAINING BIOMEDICAL POLYETHERURETHANES
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作者 Chen Huiying Feng Shiqing Sun Xuehui(Department of Chemistry, Peking University, Beijing 100871,China) 《Chinese Journal of Biomedical Engineering(English Edition)》 1996年第2期47-58,共12页
SYNTHESISANDFINESTRUCTURE-PROPERTYRELATIONSHIPSOFION-CONTAININGBIOMEDICALPOLYETHERURETHANESSYNTHESISANDFINES... SYNTHESISANDFINESTRUCTURE-PROPERTYRELATIONSHIPSOFION-CONTAININGBIOMEDICALPOLYETHERURETHANESSYNTHESISANDFINESTRUCTURE-PROPERTY... 展开更多
关键词 Ion-containing segmented polyetherurethanes Fine structure and propertyrelationships microphase separation ANTICOAGULANT property
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Designing Tough,Printable,and Adaptable Eutectogels with Multinetworks via Synergy of Rapid Orthogonal Photopolymerizations and Solvent Effect in Seconds
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作者 Jupen Liu Lijun Zhou +3 位作者 Ping Zhang Yanxia Zhao Hongqiu Wei You Yu 《CCS Chemistry》 CSCD 2024年第2期390-402,共13页
Achieving a straightforward design of tough,printable,and adaptable polymeric eutectogels is still challenging in related fields due to the uncontrollable polymerization and solvent-exchanging processes,and inherent c... Achieving a straightforward design of tough,printable,and adaptable polymeric eutectogels is still challenging in related fields due to the uncontrollable polymerization and solvent-exchanging processes,and inherent contrasting multiple networks.Here,we report a one-step synergistic strategy based on ruthenium chemistry-catalyzed photopolymerization and solvent effect for preparing high-performance eutectogels.This orthogonal ruthenium photochemistry helps multinetworks formation via phenol-coupling of gelatin and copolymerization of acrylamide(AAm)and[2-(methacryloyloxy)ethyl]trimethylammonium tetrafluoroborate(META)monomers in seconds.The obvious difference in the supramolecular interactions of free AAm monomers and polymerized units in P(AAm-co-META)with deep eutectic solvents(DESs)significantly promotes the microphase-separation behavior in eutectogels.Consequently,the in situ polymerization and microphase-separation behavior enable the as-prepared eutectogel materials to have excellent mechanical properties(stress of∼1.2 MPa),toughness(∼4.0 MJ m^(−3)),elasticity,adaptivity,and conductivity(∼0.5 S m^(−1)at room temperature).Also,the critical strength of the resultant eutectogels can be modulated by varying the DES constituents.This rapid and well-controlled synergistic approach is compatible with extrusion printing techniques to make flexible sensors with high sensitivities and response times to detect pressure in a range of 0–500 kPa.Such a general and simple strategy has application potential in biological,engineering,and material sciences. 展开更多
关键词 orthogonal chemistry visible-light photopolymerization solvent effect microphase separation adaptable polymers printable eutectogels
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Self-assembly Promoted Crystallization of Diblock Copolypeptoids in Solution
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作者 Rongye Li Yue Zhao +1 位作者 Min Lin Jing Sun 《Chinese Journal of Chemistry》 SCIE CAS CSCD 2023年第18期2305-2310,共6页
Comprehensive Summary,Great efforts have been lately devoted to fabricating well-defined nanostructures using crystallization-driven self-assembly(CDSA)strategy.The influence of self-assembly on crystallization is als... Comprehensive Summary,Great efforts have been lately devoted to fabricating well-defined nanostructures using crystallization-driven self-assembly(CDSA)strategy.The influence of self-assembly on crystallization is also of great interest.Here,a series of amphiphilic diblock copolypeptoids poly(N-allylglycine)-b-poly(N-octylglycine)modified with cysteamine hydrochloride((PNAG-g-NH_(2))-b-PNOG)were synthesized by ring-opening polymerization(ROP)and post-polymerization functionalization.The diblock copolypeptoid is comprised of one hydrophobic crystalline PNOG block and one hydrophilic amorphous block,which can aggregate into nanostructured assemblies with soluble PNAG-g-NH_(2) as the corona layer and PNOG as the inner core in aqueous solution.With a systematic study by differential scanning calorimetry(DSC)and wide-angle X-ray scattering(WAXS),we demonstrated that the self-assembly of the block copolymers strengthens the crystallization of the PNOG block. 展开更多
关键词 COPOLYMERS SELF-ASSEMBLY CRYSTALLIZATION Ring-opening polymerization microphase separation/Polypeptoids
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Macroscopic Regulation of Hierarchical Nanostructures in Liquid-crystalline Block Copolymers towards Functional Materials 被引量:3
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作者 Feng Cai Yu-Xuan Chen +1 位作者 Wen-Zhong Wang Hai-Feng Yu 《Chinese Journal of Polymer Science》 SCIE CAS CSCD 2021年第4期397-416,I0004,共21页
The great potential of liquid-crystalline block copolymers(LCBCs)containing photoresponsive mesogens toward novel applications in photonics and nanotechnology has been attracting increasing attention,due to the combin... The great potential of liquid-crystalline block copolymers(LCBCs)containing photoresponsive mesogens toward novel applications in photonics and nanotechnology has been attracting increasing attention,due to the combination of the inherent property of microphase separation of block copolymers and the hierarchically-assembled structures of liquid-crystalline polymers(LCPs).The periodically ordered nanostructures in bulk film of LCBCs can be acquired by supramolecular cooperative motion,derived from the interaction between liquid-crystalline elastic deformation and microphase separation,which are able to improve physical properties of polymer film toward advanced functional applications.Moreover,various micro/nano-patterned structures have been fabricated via light manipulation of photoresponsive LCBCs with good reproducibility and mass production.Thanks to recent developments in synthesis and polymerization techniques,diverse azobenzene-containing LCBCs have been designed,resulting in the creation of a wide variety of novel functions.This review illustrates recent progresses in macroscopic regulation of hierarchical nanostructures in LCBCs towards functional materials.The existing challenges are also discussed,showing perspectives for future studies. 展开更多
关键词 Liquid-crystalline block copolymers microphase separation Hierarchical nanostructures Functional materials
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Characterization of graded polyurethane elastomer by FTIR 被引量:2
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作者 ZHAO PeiZhong WANG Yuan Sheng +2 位作者 ZHU JinHua HUA XingYan WEN QingZhen 《Science China Chemistry》 SCIE EI CAS 2008年第1期58-61,共4页
Polyurethane elastomers with graded structure were prepared in the graded temperature field. The samples were characterized by FTIR technology. The results show that the degree of microphase separation in the samples ... Polyurethane elastomers with graded structure were prepared in the graded temperature field. The samples were characterized by FTIR technology. The results show that the degree of microphase separation in the samples decreases with the decrease of the curing temperature. As far as the molar ratio of NH2 and NCO is concerned, the sample exhibits better graded morphology when the ratio is 0.95. The transparence of the samples prepared also changes gradually, increasing along the direction, in which temperature decreases. 展开更多
关键词 FGM POLYURETHANE GRADED transparence microphase SEPARATION FTIR
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Macroscopic lamellae orientations of diblock copolymer induced by dynamic shear 被引量:1
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作者 张红东 杨玉良 《Science China Chemistry》 SCIE EI CAS 1997年第1期53-60,共8页
Computer simulation based on the coupled map lattices has been carried out for morphologies of the diblock copolymeric system under applied periodic shear deformation.The main effort is concentrated on the influence o... Computer simulation based on the coupled map lattices has been carried out for morphologies of the diblock copolymeric system under applied periodic shear deformation.The main effort is concentrated on the influence of pre-annenling history on the lamellae orientations in dynamically sheared diblock copolymers.It is found that whatever the quenching temperature is,the perpendicular orientation (i.e.the lamellae normal is parallel to the vorticity axis) is always observed if the dynamic shear deformation with shear amplitude F=1.0 and reduced shear frequency=0.005 is applied during annealing.In contrast to that,the parallel orientation (i.e.the lamellae normal is parallel to the velocity gradient direction) is observed if the dynamic shear with the same amplitude and frequency is applied to a thoroughly annealed (with the annealing time t】4 000) diblock copolymer.Therefore,it is pointed out that the selection of lamellar orientations in dynamically sheared diblock copolymers is not solely dependent on 展开更多
关键词 block copolymer microphase separation DYNAMIC SHEAR LAMELLAR morphology coupled map lattices
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