A novel class of segmented copolymers, dimethyldiphenylpolysiloxane/poly (oxytetramethylene)-polyurea (PSPEU), was synthesized from α , ω-bis (γ-aminopropyl) dimethyldiphenylpolysiloxane (APMPS), which was prepared...A novel class of segmented copolymers, dimethyldiphenylpolysiloxane/poly (oxytetramethylene)-polyurea (PSPEU), was synthesized from α , ω-bis (γ-aminopropyl) dimethyldiphenylpolysiloxane (APMPS), which was prepared by means of basic ring-opening copolymerization of octamethylcyclotetrasiloxane, hexaphenylcyclotrisiloxane and 1, 3-bis (γ-aminopropyl) tetramethyl disiloxane. The relationships between the diphenylsiloxy contents and the properties of APMPS, including refractive index, glass transition temperature, solubility parameter as well as thermal stability, were investigated; meanwhile, the thermal stability, dynamic mechanical properties, mechanical properiesas well as the antithrombogenicity in vitro of the PSPEU were also revealed.展开更多
A novel multifunctional macromolecular organolithium initiator （PD-Sn-（RLi）3） was prepared via living anionic polymerization and used for the synthesis of miktoarm star copolymers in cyclohexane. The average molec...A novel multifunctional macromolecular organolithium initiator （PD-Sn-（RLi）3） was prepared via living anionic polymerization and used for the synthesis of miktoarm star copolymers in cyclohexane. The average molecular weight, polydispersity index, microstructure and unit composition of the miktoarm star copolymers were characterized with GPC and 1H-NMR. Performances of the miktoarm star styrene-butadiene rubbers were investigated in comparison with those of the blend rubbers such as the tin-coupled star-shaped random copolymers of styrene-butadiene rubber（S-SBR）/natural rubber （NR） blend rubber and S-SBR/Cis-1, 4-polybutadiene rubber （Cis-BR） blend rubber.展开更多
In order to obtain the optimized structure rubber, a novel miktoarm star styrene-butadiene rubber （MS- SBR） was initiated by a multifunctional macromolecular initiator with polydiene arm and Sn-C bond. The propertie...In order to obtain the optimized structure rubber, a novel miktoarm star styrene-butadiene rubber （MS- SBR） was initiated by a multifunctional macromolecular initiator with polydiene arm and Sn-C bond. The properties of MS-SBR were investigated with respect to the morphology, mechanical properties, and dynamic viscoelasticity in comparison with those of the blends, natural rubber （NR）/star styrene-butadiene random rubber （S-SBR） blend rubber and cis-l,4-polybutadiene rubber （cis-BR）/S-SBR blend rubber. The samples were analyzed using transmission elec- tron microscopy （TEM）, dynamic mechanical thermal analyzer （DMTA）, and mechanical properties test. The analy- sis results show that MS-SBR possesses the desired combination of low rolling resistance and high antiskid resistance, and is promising for application in high performance tire tread.展开更多
The molecular weight of a polymer is of prime importance and greatly influences the processing and mechanical properties of the polymer. Trans-1,4-poly(butadiene-co-isoprene) multi-block copolymer rubbers(TBIR) exhibi...The molecular weight of a polymer is of prime importance and greatly influences the processing and mechanical properties of the polymer. Trans-1,4-poly(butadiene-co-isoprene) multi-block copolymer rubbers(TBIR) exhibit outstanding fatigue resistance, low heat build-up and good abrasion resistance, and are expected to be desirable candidate for high performance tire. Study on the influence of TBIR with different molecular weights on the structure and properties of TBIR and natural rubber(NR)/TBIR blends is essential to understand its contribution to the greatly improved dynamic properties of the rubber vulcanizates. TBIR with different molecular weights characterized by 1H-NMR, 13C-NMR, GPC, and DSC were highly trans-1,4-copolymers with similar chain sequence distribution and crystalline trans-1,4-polyisoprene(TPI) blocks. The green strength and modulus of TBIR increased with the increasing molecular weight.The NR/TBIR compounds filled with 40 phr carbon black were chemically cured by sulfur for the preparation of NR/TBIR vulcanizates.The compatibility between NR and TBIR, filler distribution, crosslinking bond and density, and properties of NR/TBIR vulcanizates were studied. The NR/TBIR vulcanizates showed increasing tensile strength, hardness, modulus, rebound, abrasion resistance, and flexural fatigue properties with increasing molecular weight of TBIR. Furthermore, they presented significant improvement in flexural fatigue resistance when compared with that of NR vulcanizate. The contribution mechanism of TBIR on the NR/TBIR blends was discussed. The TBIR with a wide range of molecular weight are ideal rubbers for high performance tires.展开更多
Ethylene-propylene block copolymer(EbP) is a vital component in impact polypropylene copolymer(IPC), yet its distribution in the multiphase composite material and how it influences the phase structure and the mechanic...Ethylene-propylene block copolymer(EbP) is a vital component in impact polypropylene copolymer(IPC), yet its distribution in the multiphase composite material and how it influences the phase structure and the mechanical properties are not well understood. In this work,four IPCs were investigated by atomic force microscopy-infrared(AFM-IR) to assess the phase compositions in situ, based on which in conjunction with the chain microstructure information obtained ex situ the distributions of the copolymer components were derived for each alloy. For the IPCs whose EbP comprises long P and long E segments, the EbP fraction was found to phase separate from the rubber and the PP matrix to form the cores of the disperse particles with the E-P segmented copolymer(EsP). In contrast, in the IPC with EbP composed of long P and short E segments, the EbP fraction formed an outer shell for the rubber particles with the cores comprising the EsP alone, and this IPC, containing a lower E comonomer content than its counterpart, exhibited both better impact resistance and higher flexural modulus. These results clarify how the chain structure of EbP governs the phase morphology in IPC, which in turn impacts the properties of the composite material.展开更多
通过熔体流动速率、热变形温度和力学性能等指标变化评价了ASA胶含量及用量对PC/ASA合金性能的影响。结果表明,随着ASA用量的增加,合金的热变形温度下降;可以通过ASA胶含量和用量调节合金的流动性;不论合金的组成,ASA胶含量为30%的PC/AS...通过熔体流动速率、热变形温度和力学性能等指标变化评价了ASA胶含量及用量对PC/ASA合金性能的影响。结果表明,随着ASA用量的增加,合金的热变形温度下降;可以通过ASA胶含量和用量调节合金的流动性;不论合金的组成,ASA胶含量为30%的PC/ASA合金的低温冲击强度最高;当PC/ASA比例为7∶3,ASA胶含量为30%时,PC/ASA合金的低温冲击强度最高为36 k J/m^(2)。展开更多
文摘A novel class of segmented copolymers, dimethyldiphenylpolysiloxane/poly (oxytetramethylene)-polyurea (PSPEU), was synthesized from α , ω-bis (γ-aminopropyl) dimethyldiphenylpolysiloxane (APMPS), which was prepared by means of basic ring-opening copolymerization of octamethylcyclotetrasiloxane, hexaphenylcyclotrisiloxane and 1, 3-bis (γ-aminopropyl) tetramethyl disiloxane. The relationships between the diphenylsiloxy contents and the properties of APMPS, including refractive index, glass transition temperature, solubility parameter as well as thermal stability, were investigated; meanwhile, the thermal stability, dynamic mechanical properties, mechanical properiesas well as the antithrombogenicity in vitro of the PSPEU were also revealed.
基金Supported by the National Natural Science Foundation of China(50573005)
文摘A novel multifunctional macromolecular organolithium initiator （PD-Sn-（RLi）3） was prepared via living anionic polymerization and used for the synthesis of miktoarm star copolymers in cyclohexane. The average molecular weight, polydispersity index, microstructure and unit composition of the miktoarm star copolymers were characterized with GPC and 1H-NMR. Performances of the miktoarm star styrene-butadiene rubbers were investigated in comparison with those of the blend rubbers such as the tin-coupled star-shaped random copolymers of styrene-butadiene rubber（S-SBR）/natural rubber （NR） blend rubber and S-SBR/Cis-1, 4-polybutadiene rubber （Cis-BR） blend rubber.
基金Supported by National Natural Science Foundation of China (No.50573005)
文摘In order to obtain the optimized structure rubber, a novel miktoarm star styrene-butadiene rubber （MS- SBR） was initiated by a multifunctional macromolecular initiator with polydiene arm and Sn-C bond. The properties of MS-SBR were investigated with respect to the morphology, mechanical properties, and dynamic viscoelasticity in comparison with those of the blends, natural rubber （NR）/star styrene-butadiene random rubber （S-SBR） blend rubber and cis-l,4-polybutadiene rubber （cis-BR）/S-SBR blend rubber. The samples were analyzed using transmission elec- tron microscopy （TEM）, dynamic mechanical thermal analyzer （DMTA）, and mechanical properties test. The analy- sis results show that MS-SBR possesses the desired combination of low rolling resistance and high antiskid resistance, and is promising for application in high performance tire tread.
基金financially supported by the National Basic Research Program of China(No.2015CB654700(2015CB 654706))Major Program of Shandong Province Natural Science Foundation(No.ZR2017ZA0304)Taishan Scholar Program
文摘The molecular weight of a polymer is of prime importance and greatly influences the processing and mechanical properties of the polymer. Trans-1,4-poly(butadiene-co-isoprene) multi-block copolymer rubbers(TBIR) exhibit outstanding fatigue resistance, low heat build-up and good abrasion resistance, and are expected to be desirable candidate for high performance tire. Study on the influence of TBIR with different molecular weights on the structure and properties of TBIR and natural rubber(NR)/TBIR blends is essential to understand its contribution to the greatly improved dynamic properties of the rubber vulcanizates. TBIR with different molecular weights characterized by 1H-NMR, 13C-NMR, GPC, and DSC were highly trans-1,4-copolymers with similar chain sequence distribution and crystalline trans-1,4-polyisoprene(TPI) blocks. The green strength and modulus of TBIR increased with the increasing molecular weight.The NR/TBIR compounds filled with 40 phr carbon black were chemically cured by sulfur for the preparation of NR/TBIR vulcanizates.The compatibility between NR and TBIR, filler distribution, crosslinking bond and density, and properties of NR/TBIR vulcanizates were studied. The NR/TBIR vulcanizates showed increasing tensile strength, hardness, modulus, rebound, abrasion resistance, and flexural fatigue properties with increasing molecular weight of TBIR. Furthermore, they presented significant improvement in flexural fatigue resistance when compared with that of NR vulcanizate. The contribution mechanism of TBIR on the NR/TBIR blends was discussed. The TBIR with a wide range of molecular weight are ideal rubbers for high performance tires.
基金financially supported by the National Natural Science Foundation of China (No.52073277)the Science and Technology Department of Fujian Province (No.2020HZ06019)。
文摘Ethylene-propylene block copolymer(EbP) is a vital component in impact polypropylene copolymer(IPC), yet its distribution in the multiphase composite material and how it influences the phase structure and the mechanical properties are not well understood. In this work,four IPCs were investigated by atomic force microscopy-infrared(AFM-IR) to assess the phase compositions in situ, based on which in conjunction with the chain microstructure information obtained ex situ the distributions of the copolymer components were derived for each alloy. For the IPCs whose EbP comprises long P and long E segments, the EbP fraction was found to phase separate from the rubber and the PP matrix to form the cores of the disperse particles with the E-P segmented copolymer(EsP). In contrast, in the IPC with EbP composed of long P and short E segments, the EbP fraction formed an outer shell for the rubber particles with the cores comprising the EsP alone, and this IPC, containing a lower E comonomer content than its counterpart, exhibited both better impact resistance and higher flexural modulus. These results clarify how the chain structure of EbP governs the phase morphology in IPC, which in turn impacts the properties of the composite material.
文摘通过熔体流动速率、热变形温度和力学性能等指标变化评价了ASA胶含量及用量对PC/ASA合金性能的影响。结果表明,随着ASA用量的增加,合金的热变形温度下降;可以通过ASA胶含量和用量调节合金的流动性;不论合金的组成,ASA胶含量为30%的PC/ASA合金的低温冲击强度最高;当PC/ASA比例为7∶3,ASA胶含量为30%时,PC/ASA合金的低温冲击强度最高为36 k J/m^(2)。
