In this work,a series of high strength,thermal stable and antioxidant proton exchange membranes were designed with solution processible polybenzimidazole(PBI)as the matrix and perfluorosulfonic acid(PFSA)as the fortif...In this work,a series of high strength,thermal stable and antioxidant proton exchange membranes were designed with solution processible polybenzimidazole(PBI)as the matrix and perfluorosulfonic acid(PFSA)as the fortifier for proton exchange.Solution processible PBI was successfully synthesized by introducing 4,4’-dicarboxydiphenyl ether into the molecular chains of PBI.PFSA/PBI composite membranes were obtained by solution blending and film casting.PBI and PFSA/PBI composite membranes exhibited greatly enhanced tensile strength and Young’s modulus compared to PFSA.PFSA/PBI composite membranes are stable below 300℃ which are suitable for practical application in proton exchange membrane fuel cells.The PFSA/PBI composite membranes show good dimensional stability with low water uptake and swelling rate.The PFSA/PBI composite membranes also exhibit excellent antioxidation stability with less than 5%initial mass loss over 120 h in Fenton reagent.The proton conductivity of PBI is greatly enhanced by blending with PFSA and the proton conductivities of the composite membranes are increased with the raise of PFSA content and temperature.This work offers valuable insights into the exploration of PBI based high-performance proton exchange membranes.展开更多
High-performance carbon nanofibers are highly dependent on the performance of their precursors,especially polyacrylonitrile(PAN).In this work,the copolymer of PAN(coPAN)was synthesized for electrospinning.A self-assem...High-performance carbon nanofibers are highly dependent on the performance of their precursors,especially polyacrylonitrile(PAN).In this work,the copolymer of PAN(coPAN)was synthesized for electrospinning.A self-assembling set-up was used for the stretching of single coPAN nanofibers.FTIR and Raman spectroscopies were used to characterize the chemical structure of coPAN nanofibers.Scanning electron microscopy(SEM)and atomic force microscopy(AFM)were used to monitor the morphology of single coPAN nanofibers under different drawing times.Micro-tensile test was used to determine the mechanical properties of single coPAN nanofibers.The results indicated that the drawing led to an increase in degree of molecular orientation along the fiber axis from 0.656 to 0.808,tensile strength from 304 MPa to 595 MPa,and modulus from 3.1 GPa to 12.4 GPa.This research would provide fundamental information of high-performance electrospun coPAN nanofibers and offer opportunities for the preparation of high-performance carbon nanofibers.展开更多
基金financially supported by the National Natural Science Foundation of China(Nos.22005147 and 21774053)。
文摘In this work,a series of high strength,thermal stable and antioxidant proton exchange membranes were designed with solution processible polybenzimidazole(PBI)as the matrix and perfluorosulfonic acid(PFSA)as the fortifier for proton exchange.Solution processible PBI was successfully synthesized by introducing 4,4’-dicarboxydiphenyl ether into the molecular chains of PBI.PFSA/PBI composite membranes were obtained by solution blending and film casting.PBI and PFSA/PBI composite membranes exhibited greatly enhanced tensile strength and Young’s modulus compared to PFSA.PFSA/PBI composite membranes are stable below 300℃ which are suitable for practical application in proton exchange membrane fuel cells.The PFSA/PBI composite membranes show good dimensional stability with low water uptake and swelling rate.The PFSA/PBI composite membranes also exhibit excellent antioxidation stability with less than 5%initial mass loss over 120 h in Fenton reagent.The proton conductivity of PBI is greatly enhanced by blending with PFSA and the proton conductivities of the composite membranes are increased with the raise of PFSA content and temperature.This work offers valuable insights into the exploration of PBI based high-performance proton exchange membranes.
基金financially supported by the National Natural Science Foundation of China(Nos.21774053,21975111,and 51903123)Natural Science Foundation of Jiangsu Province(No.BK20190760)+1 种基金Major Special Projects of Jiangxi Provincial Department of Science and Technology(No.20114ABF05100)Technology Plan Landing Project of Jiangxi Provincial Department of Education(No.GCJ2011-24)。
文摘High-performance carbon nanofibers are highly dependent on the performance of their precursors,especially polyacrylonitrile(PAN).In this work,the copolymer of PAN(coPAN)was synthesized for electrospinning.A self-assembling set-up was used for the stretching of single coPAN nanofibers.FTIR and Raman spectroscopies were used to characterize the chemical structure of coPAN nanofibers.Scanning electron microscopy(SEM)and atomic force microscopy(AFM)were used to monitor the morphology of single coPAN nanofibers under different drawing times.Micro-tensile test was used to determine the mechanical properties of single coPAN nanofibers.The results indicated that the drawing led to an increase in degree of molecular orientation along the fiber axis from 0.656 to 0.808,tensile strength from 304 MPa to 595 MPa,and modulus from 3.1 GPa to 12.4 GPa.This research would provide fundamental information of high-performance electrospun coPAN nanofibers and offer opportunities for the preparation of high-performance carbon nanofibers.