Pub Date : 2024-01-31DOI: 10.1177/09540083241229209
Xuhai Xiong, Lei Yao, Rong Ren, Donghui Liu, Na Li
A new series of high-temperature resistant bisphthalonitrile resins containing trifluoromethyl groups were prepared based on 4,4’-(hexafluoroisopropylidene) bisphthalonitrile (BFPh), which was toughened by hexafluoroisopropylidene-containing poly (aryl ether nitrile) oligomer capped by phthalonitrile (FPEN-Ph) in the different content. In addition, glass fiber reinforced composites were prepared by hot pressing process. The structure of the oligomer was characterized by FTIR and 1HNMR. The curing behavior of the blends was studied by DSC. Thermal stability and mechanical properties were also studied. The results showed that the introduction of appropriate content of FPEN-Ph could improve the reactivity of the curing reaction. TGA and DMA results showed that the cured polymers and composites had excellent thermal properties. The residual mass of FPEN-Ph content of 10% at 800°C was 72.4%, and the 5% thermal degradation temperature (T5%) under inert atmosphere was 530°C. The flexural strength of glass fiber reinforced composites was about 592.7 MPa, and the shear strength was about 61.6 MPa, showing excellent mechanical properties. The high-tech thermosetting resin was toughened and enhanced at the same time without reducing heat resistance.
{"title":"Preparation and properties of high-temperature resistant bisphthalonitrile resins containing trifluoromethyl groups reinforced by poly (aryl ether nitrile) capped by phthalonitrile and composites","authors":"Xuhai Xiong, Lei Yao, Rong Ren, Donghui Liu, Na Li","doi":"10.1177/09540083241229209","DOIUrl":"https://doi.org/10.1177/09540083241229209","url":null,"abstract":"A new series of high-temperature resistant bisphthalonitrile resins containing trifluoromethyl groups were prepared based on 4,4’-(hexafluoroisopropylidene) bisphthalonitrile (BFPh), which was toughened by hexafluoroisopropylidene-containing poly (aryl ether nitrile) oligomer capped by phthalonitrile (FPEN-Ph) in the different content. In addition, glass fiber reinforced composites were prepared by hot pressing process. The structure of the oligomer was characterized by FTIR and 1HNMR. The curing behavior of the blends was studied by DSC. Thermal stability and mechanical properties were also studied. The results showed that the introduction of appropriate content of FPEN-Ph could improve the reactivity of the curing reaction. TGA and DMA results showed that the cured polymers and composites had excellent thermal properties. The residual mass of FPEN-Ph content of 10% at 800°C was 72.4%, and the 5% thermal degradation temperature (T5%) under inert atmosphere was 530°C. The flexural strength of glass fiber reinforced composites was about 592.7 MPa, and the shear strength was about 61.6 MPa, showing excellent mechanical properties. The high-tech thermosetting resin was toughened and enhanced at the same time without reducing heat resistance.","PeriodicalId":12932,"journal":{"name":"High Performance Polymers","volume":null,"pages":null},"PeriodicalIF":2.1,"publicationDate":"2024-01-31","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"139949557","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2024-01-03DOI: 10.1177/09540083231225284
Xinjia Yang, Keru Song, Dongyu Zhao
The graphene/nanonickel composites(Ni/RGO) were prepared by liquid phase reduction method, and the graphene/nanonickel epoxy composites(Ni/RGO/EP) were prepared by in-situ polymerization method. The glass transition temperature (Tg) of the modified epoxy resin was increased by 19°C compared to EP with 2.1 wt% Ni/RGO loading. The tensile strength and hardness increased by 65% and 18%, the impact strength is increased by 10.053 KJ·m−2 compared to EP, and the shear strength reaches 34.78 MPa for the Ni/RGO/EP with 1.7 wt% Ni/RGO loading. It can be seen, that the addition of Ni/RGO greatly improves the heat resistance and mechanical properties of epoxy resin when the Ni/RGO are evenly dispersed into the epoxy resin by emulsion dispersion method.
{"title":"Preparation and mechanical properties of Ni/RGO reinforced epoxy resin composites","authors":"Xinjia Yang, Keru Song, Dongyu Zhao","doi":"10.1177/09540083231225284","DOIUrl":"https://doi.org/10.1177/09540083231225284","url":null,"abstract":"The graphene/nanonickel composites(Ni/RGO) were prepared by liquid phase reduction method, and the graphene/nanonickel epoxy composites(Ni/RGO/EP) were prepared by in-situ polymerization method. The glass transition temperature (Tg) of the modified epoxy resin was increased by 19°C compared to EP with 2.1 wt% Ni/RGO loading. The tensile strength and hardness increased by 65% and 18%, the impact strength is increased by 10.053 KJ·m<jats:sup>−2</jats:sup> compared to EP, and the shear strength reaches 34.78 MPa for the Ni/RGO/EP with 1.7 wt% Ni/RGO loading. It can be seen, that the addition of Ni/RGO greatly improves the heat resistance and mechanical properties of epoxy resin when the Ni/RGO are evenly dispersed into the epoxy resin by emulsion dispersion method.","PeriodicalId":12932,"journal":{"name":"High Performance Polymers","volume":null,"pages":null},"PeriodicalIF":2.1,"publicationDate":"2024-01-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"139949424","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2023-12-30DOI: 10.1177/09540083231225290
Huanhuan Gao, Xiaozhou Zhang, X. Jian, Jinyan Wang
In this study, the melt polycondensation reaction of 9,9’- bis(4-hydroxyphenyl)fluoride (BHPF) and diphenyl carbonate (DPC) was catalyzed using three ionic liquids (ILs) and a conventional alkali metal as catalysts. The optimal IL catalysts were determined to be [BMmim][BF4] ionic liquid catalysts, and the catalytic mechanism was investigated. Furthermore, the optimum process conditions were identified: the optimal amount of [BMmim][BF4] was 0.05 mol% based on DPC, the polycondensation temperature was set at 200°C for a duration of 3 h, followed by polymerization at 280°C for another 3 h. As a result, the Mn value of poly(9,9-bis(4-hydroxyphenyl) carbonate) (PFC) reached up to 41387 g/mol with a glass transition temperature band of approximately 254°C and Td-5% value of around 436°C.
{"title":"Preparation of high temperature resistant polycarbonate via ionic liquid activation of bisphenol fluorene under mild conditions","authors":"Huanhuan Gao, Xiaozhou Zhang, X. Jian, Jinyan Wang","doi":"10.1177/09540083231225290","DOIUrl":"https://doi.org/10.1177/09540083231225290","url":null,"abstract":"In this study, the melt polycondensation reaction of 9,9’- bis(4-hydroxyphenyl)fluoride (BHPF) and diphenyl carbonate (DPC) was catalyzed using three ionic liquids (ILs) and a conventional alkali metal as catalysts. The optimal IL catalysts were determined to be [BMmim][BF4] ionic liquid catalysts, and the catalytic mechanism was investigated. Furthermore, the optimum process conditions were identified: the optimal amount of [BMmim][BF4] was 0.05 mol% based on DPC, the polycondensation temperature was set at 200°C for a duration of 3 h, followed by polymerization at 280°C for another 3 h. As a result, the Mn value of poly(9,9-bis(4-hydroxyphenyl) carbonate) (PFC) reached up to 41387 g/mol with a glass transition temperature band of approximately 254°C and Td-5% value of around 436°C.","PeriodicalId":12932,"journal":{"name":"High Performance Polymers","volume":null,"pages":null},"PeriodicalIF":2.1,"publicationDate":"2023-12-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"139140332","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2023-12-28DOI: 10.1177/09540083231224608
Mukesh Kumar, R. Goyal, S. Sharma
Poly(ether-ketone)/fly ash (FA) composites reinforced with 0-30 wt% FA were fabricated using ball milling followed by hot compaction. The composites were investigated for mechanical and viscoelastic properties. Scanning electron microscopy revealed excellent dispersion and good adhesion of FA particles with the matrix. The addition of FA increased the microhardness by 70% and the storage modulus (below glass transition) by 75%. The reinforcing efficiency was better above the glass transition, which increased to around 177% at 250°C. This research indicates that the FA can be used as an alternative reinforcement of costly ceramic powder for the electronic packaging substrate or printed circuit board applications.
采用球磨法和热压实法制造了 0-30 wt% FA 增强的聚（醚酮）/粉煤灰（FA）复合材料。对复合材料的机械和粘弹性能进行了研究。扫描电子显微镜显示，FA 颗粒的分散性极佳，与基体的粘附性良好。添加 FA 后，微硬度提高了 70%，储存模量（低于玻璃化转变）提高了 75%。玻璃化转变以上的强化效率更高，在 250°C 时增至约 177%。这项研究表明，在电子封装基板或印刷电路板应用中，FA 可用作昂贵陶瓷粉末的替代增强材料。
{"title":"Viscoelastic behaviour of poly(ether-ketone)/fly ash composites fabricated by powder metallurgical route","authors":"Mukesh Kumar, R. Goyal, S. Sharma","doi":"10.1177/09540083231224608","DOIUrl":"https://doi.org/10.1177/09540083231224608","url":null,"abstract":"Poly(ether-ketone)/fly ash (FA) composites reinforced with 0-30 wt% FA were fabricated using ball milling followed by hot compaction. The composites were investigated for mechanical and viscoelastic properties. Scanning electron microscopy revealed excellent dispersion and good adhesion of FA particles with the matrix. The addition of FA increased the microhardness by 70% and the storage modulus (below glass transition) by 75%. The reinforcing efficiency was better above the glass transition, which increased to around 177% at 250°C. This research indicates that the FA can be used as an alternative reinforcement of costly ceramic powder for the electronic packaging substrate or printed circuit board applications.","PeriodicalId":12932,"journal":{"name":"High Performance Polymers","volume":null,"pages":null},"PeriodicalIF":2.1,"publicationDate":"2023-12-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"139149910","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Polyimide (PI) film have been synthesized and used extensively in energy transmission, wind power generation, new energy vehicles, lidar, and high-power weapons, et al. Nevertheless, it is still challenge to further improve the breakdown strength and dielectric constant of PI film. After the powders of Al0.5xNb0.5xSi1-xO2 (NASO (x mol%)) have been fabricated, it was analyzed that the effect of doping elements Al3+ and Nb5+ on the surface chemistry and microstructure of the NASO powder. And then a small amount of NASO powder was polymerized in situ with PI matrix material, and the effects of NASO on dielectric properties and breakdown strength of the NASO/PI composites were analyzed. The results showed that the introduction of the doping elements Al3+ and Nb5+ favors could be conductive to the formation of oxygen vacancies on the surface of the NASO particle, which improved the surface activity and chemical reactivity of the NASO particle. The PI matrix can efficiently capture additional charges and enhance the insulating characteristics of the NASO/PI composite by properly doping NASO fillers with specific defect concentrations. In the results the breakdown strength of 1 vol% NASO (1 mol%)/PI composites reaches 334.38 kV/mm, which is a 19.6% higher than that of PI. Because the traps in the fillers capture and suppress the carrier transport to enhance the insulating properties of the composites. This work offers a novel synthesis method to simultaneously produce polymer dielectrics with high insulation and high polarization.
{"title":"Preparation and dielectric properties of polyimide-based composites with Al-Nb co-doped SiO2","authors":"Wenchao Zhang, Qiang Fu, Qixin Yuan, Han Li, Dong Yue, Yu Feng, Qingguo Chen, Jinghua Yin","doi":"10.1177/09540083231224158","DOIUrl":"https://doi.org/10.1177/09540083231224158","url":null,"abstract":"Polyimide (PI) film have been synthesized and used extensively in energy transmission, wind power generation, new energy vehicles, lidar, and high-power weapons, et al. Nevertheless, it is still challenge to further improve the breakdown strength and dielectric constant of PI film. After the powders of Al0.5xNb0.5xSi1-xO2 (NASO (x mol%)) have been fabricated, it was analyzed that the effect of doping elements Al3+ and Nb5+ on the surface chemistry and microstructure of the NASO powder. And then a small amount of NASO powder was polymerized in situ with PI matrix material, and the effects of NASO on dielectric properties and breakdown strength of the NASO/PI composites were analyzed. The results showed that the introduction of the doping elements Al3+ and Nb5+ favors could be conductive to the formation of oxygen vacancies on the surface of the NASO particle, which improved the surface activity and chemical reactivity of the NASO particle. The PI matrix can efficiently capture additional charges and enhance the insulating characteristics of the NASO/PI composite by properly doping NASO fillers with specific defect concentrations. In the results the breakdown strength of 1 vol% NASO (1 mol%)/PI composites reaches 334.38 kV/mm, which is a 19.6% higher than that of PI. Because the traps in the fillers capture and suppress the carrier transport to enhance the insulating properties of the composites. This work offers a novel synthesis method to simultaneously produce polymer dielectrics with high insulation and high polarization.","PeriodicalId":12932,"journal":{"name":"High Performance Polymers","volume":null,"pages":null},"PeriodicalIF":2.1,"publicationDate":"2023-12-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"139162135","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2023-12-18DOI: 10.1177/09540083231222593
Xiaolu Wu, Zhaolu Qin, Wenchao Zhang, Rongjie Yang
Fully condensed polyphenylsilsesquioxanes have been prepared via the hydrolysis and condensation of the same phenyltrimethoxysilane (PTMS) monomer in different concentrations. The effect of monomer concentration on molecular structure of the final products has been thoroughly investigated. Cage structured polyphenylsilsesquioxane (OPS) and ladder-like structured polyphenylsilsesquioxane (L-PPSQ) can be selectively synthesized from the same starting materials at lower and higher initial monomer concentrations. Meanwhile, online infrared detector, React IR TM15 was used to monitor the real time variation of the concentration and characteristic absorption peaks of any intermediate products that may exist. Then, React IR TM15 coupled with 29Si nuclear magnetic resonance spectroscopy (NMR), gel permeation chromatography (GPC) and matrix-assisted laser desorption/ionization-time of flight mass spectrometry (MALDI-TOF-MS) were used to monitor and identify the intermediate species during the reaction. Mechanism studies indicated that the condensation reaction of OPS and L-PPSQ both proceed through a T1 structure dimer, which was formed by the quick hydrolysis of the PTMS monomer. As confirmed by 29Si-NMR, GPC and MALDI-TOF-MS, the synthesis mechanisms of OPS and L-PPSQ during the hydrolysis-condensation reactions were delineated.
{"title":"Influence of monomer concentration on structures of fully condensed polyphenylsilsesquioxanes","authors":"Xiaolu Wu, Zhaolu Qin, Wenchao Zhang, Rongjie Yang","doi":"10.1177/09540083231222593","DOIUrl":"https://doi.org/10.1177/09540083231222593","url":null,"abstract":"Fully condensed polyphenylsilsesquioxanes have been prepared via the hydrolysis and condensation of the same phenyltrimethoxysilane (PTMS) monomer in different concentrations. The effect of monomer concentration on molecular structure of the final products has been thoroughly investigated. Cage structured polyphenylsilsesquioxane (OPS) and ladder-like structured polyphenylsilsesquioxane (L-PPSQ) can be selectively synthesized from the same starting materials at lower and higher initial monomer concentrations. Meanwhile, online infrared detector, React IR TM15 was used to monitor the real time variation of the concentration and characteristic absorption peaks of any intermediate products that may exist. Then, React IR TM15 coupled with 29Si nuclear magnetic resonance spectroscopy (NMR), gel permeation chromatography (GPC) and matrix-assisted laser desorption/ionization-time of flight mass spectrometry (MALDI-TOF-MS) were used to monitor and identify the intermediate species during the reaction. Mechanism studies indicated that the condensation reaction of OPS and L-PPSQ both proceed through a T1 structure dimer, which was formed by the quick hydrolysis of the PTMS monomer. As confirmed by 29Si-NMR, GPC and MALDI-TOF-MS, the synthesis mechanisms of OPS and L-PPSQ during the hydrolysis-condensation reactions were delineated.","PeriodicalId":12932,"journal":{"name":"High Performance Polymers","volume":null,"pages":null},"PeriodicalIF":2.1,"publicationDate":"2023-12-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"138963720","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
High-performance co-polyimide (co-PI) fibers derived from 3,3`4,4`-biphenyldianhydride (BPDA), p-phenylenediamine (p-PDA) and 2-(4-aminophenyl)-5-amino-benzimidazole (BIA) were prepared via the wet spinning and dry-jet wet spinning method, respectively. The distinctions between wet spinning and dry-jet wet spinning processes on the structures and properties of co-PI fibers were systematically investigated. The co-PI fibers prepared by dry-jet wet spinning exhibited smoother surface morphology and higher mechanical properties than those of co-PI prepared by wet spinning. Wide-angle X-ray diffraction (WAXD) results showed that the co-PI fibers prepared by dry-jet wet spinning exhibited highly oriented structure along the fiber direction along with a low degree of lateral packing order in the transverse direction. Small-angle X-ray scattering (SAXS) revealed that the radius, length, misorientation and internal surface roughness of the microvoids in the co-PI fibers prepared by the dry-jet wet spinning are lower than those in co-PI fibers prepared by wet spinning. Moreover, the effect of air layer height, as well as the heat treatment on the structure and properties of fibers during the dry-jet wet spinning process, was also studied. The tensile strength and modulus of co-PI fibers prepared by dry-jet wet spinning reached 2.72 GPa and 114.29 GPa, respectively, with an air layer height of 10 mm and a heat stretching temperature of 440°C.
通过湿法纺丝和干法喷气湿法纺丝，分别制备了由3,3,4,4'-联苯二酐（BPDA）、对苯二胺（p-PDA）和2-(4-氨基苯基)-5-氨基苯并咪唑（BIA）衍生的高性能共聚酰亚胺（co-PI）纤维。系统研究了湿法纺丝和干法喷气湿法纺丝工艺对共PI纤维结构和性能的影响。与湿法纺丝相比，干喷湿法纺丝制备的共 PI 纤维表面形态更光滑，机械性能更高。广角 X 射线衍射（WAXD）结果表明，干喷湿纺制备的共 PI 纤维沿纤维方向呈现出高度取向结构，横向上的横向堆积有序度较低。小角 X 射线散射（SAXS）显示，干喷湿法纺丝制备的共 PI 纤维中微空洞的半径、长度、错向度和内表面粗糙度均低于湿法纺丝制备的共 PI 纤维。此外，还研究了干喷湿纺过程中空气层高度以及热处理对纤维结构和性能的影响。在空气层高度为 10 毫米、热拉伸温度为 440°C 的条件下，干喷湿纺制备的共 PI 纤维的拉伸强度和模量分别达到了 2.72 GPa 和 114.29 GPa。
{"title":"Fabrication of high performance polyimide fibers by dry-jet wet spinning technology","authors":"Xiaowei Wang, Mengying Zhang, Hongqing Niu, Dezhen Wu","doi":"10.1177/09540083231221248","DOIUrl":"https://doi.org/10.1177/09540083231221248","url":null,"abstract":"High-performance co-polyimide (co-PI) fibers derived from 3,3`4,4`-biphenyldianhydride (BPDA), p-phenylenediamine (p-PDA) and 2-(4-aminophenyl)-5-amino-benzimidazole (BIA) were prepared via the wet spinning and dry-jet wet spinning method, respectively. The distinctions between wet spinning and dry-jet wet spinning processes on the structures and properties of co-PI fibers were systematically investigated. The co-PI fibers prepared by dry-jet wet spinning exhibited smoother surface morphology and higher mechanical properties than those of co-PI prepared by wet spinning. Wide-angle X-ray diffraction (WAXD) results showed that the co-PI fibers prepared by dry-jet wet spinning exhibited highly oriented structure along the fiber direction along with a low degree of lateral packing order in the transverse direction. Small-angle X-ray scattering (SAXS) revealed that the radius, length, misorientation and internal surface roughness of the microvoids in the co-PI fibers prepared by the dry-jet wet spinning are lower than those in co-PI fibers prepared by wet spinning. Moreover, the effect of air layer height, as well as the heat treatment on the structure and properties of fibers during the dry-jet wet spinning process, was also studied. The tensile strength and modulus of co-PI fibers prepared by dry-jet wet spinning reached 2.72 GPa and 114.29 GPa, respectively, with an air layer height of 10 mm and a heat stretching temperature of 440°C.","PeriodicalId":12932,"journal":{"name":"High Performance Polymers","volume":null,"pages":null},"PeriodicalIF":2.1,"publicationDate":"2023-12-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"139002795","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
A series of modified aromatic oxadiazole polymers were synthesized via condensation reactions of terephthalic dihydrazide (TPH) and varying amounts of Trimesic acid (H3BTC) in polyphosphoric acid (PPA). Pentaerythritol was introduced to construct intermolecular hydrogen bonds among polymeric chains, resulting in a three-dimensional network structure, and correlations between H-bonds and mechanic properties are discussed. Structures and mechanic properties of the polymers were characterized and analyzed. By investigation of molecular structure and membrane formation process of chemically modified and hydrogen bond-regulated polymer membranes, it was found that the modified polymer membranes retain the unique thermal stability, chemical stability, and good hydrophobicity of the POD rigid polymer. Additionally, hydrogen bonds not only significantly improve the overall quality of the membrane, but also play an important role in enhancing the mechanical properties of the membrane, as demonstrated in the highest observed of up to a maximum of 167.19 MPa. Furthermore, impact of H3BCT modification on light absorption and fluorescence performance of T-PODx is also analyzed and discussed in this paper.
{"title":"Fabrication and characterization of modified POD membranes with ultra-high tensile strength through hydrogen bonding functioning and copolymerization","authors":"Mengxiang Huang, Lihong Li, Wen-Guang Xie, Ni Yan, Limin Yuan, Zhiqiang Zhu, Zhenlin Jiang","doi":"10.1177/09540083231219780","DOIUrl":"https://doi.org/10.1177/09540083231219780","url":null,"abstract":"A series of modified aromatic oxadiazole polymers were synthesized via condensation reactions of terephthalic dihydrazide (TPH) and varying amounts of Trimesic acid (H3BTC) in polyphosphoric acid (PPA). Pentaerythritol was introduced to construct intermolecular hydrogen bonds among polymeric chains, resulting in a three-dimensional network structure, and correlations between H-bonds and mechanic properties are discussed. Structures and mechanic properties of the polymers were characterized and analyzed. By investigation of molecular structure and membrane formation process of chemically modified and hydrogen bond-regulated polymer membranes, it was found that the modified polymer membranes retain the unique thermal stability, chemical stability, and good hydrophobicity of the POD rigid polymer. Additionally, hydrogen bonds not only significantly improve the overall quality of the membrane, but also play an important role in enhancing the mechanical properties of the membrane, as demonstrated in the highest observed of up to a maximum of 167.19 MPa. Furthermore, impact of H3BCT modification on light absorption and fluorescence performance of T-PODx is also analyzed and discussed in this paper.","PeriodicalId":12932,"journal":{"name":"High Performance Polymers","volume":null,"pages":null},"PeriodicalIF":2.1,"publicationDate":"2023-12-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"138606691","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
In this study, 4-biphenyl-3,5-diaminobenzoate (E- m-PDA) was synthesized by three steps using 3,5-dinitrobenzoic acid as a starting material. Two series of colorless polyimides (CPIs) PI-(1a-1d) and PI-(2a-2d) were prepared by traditional two-step polycondensation of m-phenylenediamine ( m-PDA) based diamines with different pendant groups (-H, CF 3 , COOH and biphenyl ester) with aromatic dianhydrides BPADA and 6FDA, respectively. All of the prepared CPIs exhibited high thermal stability with 5% weight loss at temperatures ranging from 428 to 539°C in nitrogen, and glass transition temperatures ( T g s) ranging from 228 to 332°C. These PI films displayed a UV-vis absorption cut-off wavelength at 338–376 nm and transparency of 76%–89% at a wavelength of 450 nm. Both series of colorless PI films also showed low birefringence values of 0.0021–0.0100. In addition, the optical retardations of these CPIs were extremely low (48–220 nm), indicating low optical anisotropy of these CPI films. Colorless PI film PI-2d prepared based on E- m-PDA and 6FDA had good comprehensive properties of low birefringence ([Formula: see text] n of 0.0064), high T g (319°C) and excellent transparency ( T 450 of 88%).
{"title":"Synthesis and characterization of low retardation colorless polyimides containing <i>m</i>-phenylenediamine with different pendant groups","authors":"Xiaohong Li, Nafeesa Mushtaq, Jinglei Xing, Guofei Chen, Xingzhong Fang","doi":"10.1177/09540083231208019","DOIUrl":"https://doi.org/10.1177/09540083231208019","url":null,"abstract":"In this study, 4-biphenyl-3,5-diaminobenzoate (E- m-PDA) was synthesized by three steps using 3,5-dinitrobenzoic acid as a starting material. Two series of colorless polyimides (CPIs) PI-(1a-1d) and PI-(2a-2d) were prepared by traditional two-step polycondensation of m-phenylenediamine ( m-PDA) based diamines with different pendant groups (-H, CF 3 , COOH and biphenyl ester) with aromatic dianhydrides BPADA and 6FDA, respectively. All of the prepared CPIs exhibited high thermal stability with 5% weight loss at temperatures ranging from 428 to 539°C in nitrogen, and glass transition temperatures ( T g s) ranging from 228 to 332°C. These PI films displayed a UV-vis absorption cut-off wavelength at 338–376 nm and transparency of 76%–89% at a wavelength of 450 nm. Both series of colorless PI films also showed low birefringence values of 0.0021–0.0100. In addition, the optical retardations of these CPIs were extremely low (48–220 nm), indicating low optical anisotropy of these CPI films. Colorless PI film PI-2d prepared based on E- m-PDA and 6FDA had good comprehensive properties of low birefringence ([Formula: see text] n of 0.0064), high T g (319°C) and excellent transparency ( T 450 of 88%).","PeriodicalId":12932,"journal":{"name":"High Performance Polymers","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2023-11-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"135272892","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2023-10-31DOI: 10.1177/09540083231212148
Lu Shen, Jian Xing
Polyphenylene sulfide (PPS) with unique performance advantages and development potential is widely used in electronics, aerospace, environmental protection, automobile, machinery, textile, chemical, pharmacy, environmental protection and other industries. The researches on PPS material are constantly advancing and improving in both quantity and quality. To clarify the progress and status, and to explore current focus and development trend of PPS at a global level, the bibliometric analysis was used based on Web of Science Core Collection database. 1118 papers were retrieved, and countries or regions, institutions, journals, authors, research areas, author keywords, and highly cited articles were discussed in detail. The results of bibliometric analysis show that China was the dominant country in terms of contributions of paper output, followed by the USA, South Korea, Japan, India, and Germany. Germany and China both were the most active partner which worked with other high productive countries. “Polymer science” was the most attractive research area with 451 papers involved in. “Journal of Applied Polymer Science” was the most comprehensive source of PPS material publications and with the highest h-index. The author keywords “mechanical property”, “behavior”, “composite”, “morphology”, “kinetics”, “friction”, “tribological property” and “crystallization” reflected a high level attention and hot topics for PPS. Based on the results of bibliometric analysis, the research progress and achievements of preparation, performance improvement and application field expansion in recent years were summarized and explained. To achieve more comprehensive performance and to be suitable for more special applications in various fields, the enhancement and toughening of PPS, the modification by blending or alloying with other polymers or other reinforcing materials, the production of PPS ultrafine fiber and PPS membrane were shownas the research emphasis.
聚苯硫醚(PPS)以其独特的性能优势和发展潜力，广泛应用于电子、航空航天、环保、汽车、机械、纺织、化工、制药、环保等行业。PPS材料的研究在数量和质量上都在不断推进和提高。基于Web of Science Core Collection数据库，采用文献计量学分析方法，明确PPS的研究进展和现状，探讨PPS在全球范围内的研究重点和发展趋势。检索论文1118篇，详细讨论了国家或地区、机构、期刊、作者、研究领域、作者关键词、高被引文章等。文献计量分析结果显示，中国是论文产出贡献最大的国家，其次是美国、韩国、日本、印度和德国。德国和中国都是与其他高生产率国家合作最积极的伙伴。“高分子科学”是最具吸引力的研究领域，共涉及451篇论文。《Journal of Applied Polymer Science》是PPS材料出版物最全面的来源，h指数最高。关键词“力学性能”、“行为”、“复合”、“形貌”、“动力学”、“摩擦”、“摩擦学性能”和“结晶”反映了PPS的高度关注和热门话题。在文献计量分析的基础上，对近年来在制备、性能改进和应用领域拓展等方面的研究进展和成果进行了总结和说明。为了使聚苯乙烯具有更全面的性能和更广泛的应用领域，聚苯乙烯的增强增韧、与其他聚合物或增强材料共混或合金化改性、聚苯乙烯超细纤维和聚苯乙烯膜的生产是研究的重点。
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