Epoxy resin is widely used in electronic packaging due to its exceptional performance,particularly the low-temperature curable thiol/epoxy system,which effectively minimizes thermal damage to sensitive electronic comp...Epoxy resin is widely used in electronic packaging due to its exceptional performance,particularly the low-temperature curable thiol/epoxy system,which effectively minimizes thermal damage to sensitive electronic components.However,the majority of commercial thiol curing agents contain hydrolysable ester bonds and lack rigid structures,which induces most of thiol/epoxy systems still suffering from unsatisfactory heat resistance and hygrothermal resistance,significantly hindering their application in electronic packaging.In this study,we synthesized a tetrafunctional thiol compound,bis[3-(3-sulfanylpropyl)-4-(3-sulfanylpropoxy)phenyl]sulfone(TMBPS)with rigid and ester-free structures to replace traditional commercial thiol curing agents,pentaerythritol tetra(3-mercaptopropionate)(PETMP).Compared to the PETMP/epoxy system,the TMBPS/epoxy system exhibited superior comprehensive properties.The rigid structures of bisphenol S-type tetrathiol enhanced the heat resistance and mechanical properties of TMBPS/epoxy resin cured products,outperforming those of PETMP/epoxy resin cured products.Notably,the glass transition temperature of TMBPS/epoxy resin cured products was 74.2℃which was 11.8°C higher than that of PETMP cured products.Moreover,the ester-free structure in TMBPS contributed to its enhanced resistance to chemicals and hygrothermal conditions.After undergoing 1000 h of hightemperature and high-humidity aging,the tensile strength and adhesion strength of TMBPS-cured products were 73.33 MPa and 3.39 MPa,respectively exceeding 100%and 40%of their initial values,while PETMP-cured products exhibited a complete loss of both tensile strength and adhesion strength.This study provides a strategy for obtaining thermosetting polymers that can be cured at low temperatures and exhibit excellent comprehensive properties.展开更多
This work investigated the effect of Na_(2)CO_(3)on the char structures of cellulose and lignin,respective-ly,and examined the electrochemi-cal performance of the char by act-ing as an active material for coin cells.T...This work investigated the effect of Na_(2)CO_(3)on the char structures of cellulose and lignin,respective-ly,and examined the electrochemi-cal performance of the char by act-ing as an active material for coin cells.The morphology of char can be significantly steered by the con-centration of Na_(2)CO_(3).Scanning electron microscopy analysis demonstrated that the intro-duction of Na_(2)CO_(3)into cellulose at an appropriate concentration led to the formation of tubular structure on its surface after pyrolysis,whereas the tubular structure was absent in the lignin char with the addition of Na_(2)CO_(3)at any concentrations.X-ray diffraction and Ra-man spectroscopy characterizations revealed that all the obtained chars from both cellulose and lignin,with or without Na_(2)CO_(3),were ascribed to non-crystalline graphite.Nevertheless,the crystal orientation of graphite from cellulose and lignin changed after the catalysis of Na_(2)CO_(3).Further electrochemical tests showed that cellulose char had a higher sodium stor-age capacity than that of lignin char.The excellent electrochemical performance of carbon materials derived from cellulose might hold a prospective application in the field of energy storage.展开更多
Developing of economic and efficient catalysts is critical for the application of electroreduction of carbon dioxide to highly valuable chemicals.Herein,we present a facile method to synthesize N-doped hieratically po...Developing of economic and efficient catalysts is critical for the application of electroreduction of carbon dioxide to highly valuable chemicals.Herein,we present a facile method to synthesize N-doped hieratically porous carbon through pyrolysis of petroleum pitch followed by ammonia etching.We found mesopores are favored formation by removing of asphaltene from petroleum pitch during the carbonation process.Simultaneously,ammonia etching can not only increase the pyridinic-N content,but also upgrade the ratio of meso-to micro-pores of carbon materials.Using the N-doped hieratically porous carbon as catalyst for carbon dioxide electroreduction,the Faradaic efficiency of carbon monoxide reaches 83%at-0.9 V vs.the reversible hydrogen electrode(RHE)in 0.1 M KHCO_(3).This superior performance is attributed to the synergistic effects of highly pyridinic-N content in conjunction with the hieratically porous architecture,rendering abundant exposed and accessible active sites for electroreduction of CO_(2).Our work provides a new strategy for the large-scale preparation of high-performance,low-cost catalysts for CO_(2) electroreduction.展开更多
基金the support of the Science and Technology Commission of Shanghai Municipality(STCSM,No.20dz1203600)the Experimental Center of Materials Science and Engineering in Tongji University。
文摘Epoxy resin is widely used in electronic packaging due to its exceptional performance,particularly the low-temperature curable thiol/epoxy system,which effectively minimizes thermal damage to sensitive electronic components.However,the majority of commercial thiol curing agents contain hydrolysable ester bonds and lack rigid structures,which induces most of thiol/epoxy systems still suffering from unsatisfactory heat resistance and hygrothermal resistance,significantly hindering their application in electronic packaging.In this study,we synthesized a tetrafunctional thiol compound,bis[3-(3-sulfanylpropyl)-4-(3-sulfanylpropoxy)phenyl]sulfone(TMBPS)with rigid and ester-free structures to replace traditional commercial thiol curing agents,pentaerythritol tetra(3-mercaptopropionate)(PETMP).Compared to the PETMP/epoxy system,the TMBPS/epoxy system exhibited superior comprehensive properties.The rigid structures of bisphenol S-type tetrathiol enhanced the heat resistance and mechanical properties of TMBPS/epoxy resin cured products,outperforming those of PETMP/epoxy resin cured products.Notably,the glass transition temperature of TMBPS/epoxy resin cured products was 74.2℃which was 11.8°C higher than that of PETMP cured products.Moreover,the ester-free structure in TMBPS contributed to its enhanced resistance to chemicals and hygrothermal conditions.After undergoing 1000 h of hightemperature and high-humidity aging,the tensile strength and adhesion strength of TMBPS-cured products were 73.33 MPa and 3.39 MPa,respectively exceeding 100%and 40%of their initial values,while PETMP-cured products exhibited a complete loss of both tensile strength and adhesion strength.This study provides a strategy for obtaining thermosetting polymers that can be cured at low temperatures and exhibit excellent comprehensive properties.
基金supported by Foundation Project of Jihua Laboratory(X200191TL200).
文摘This work investigated the effect of Na_(2)CO_(3)on the char structures of cellulose and lignin,respective-ly,and examined the electrochemi-cal performance of the char by act-ing as an active material for coin cells.The morphology of char can be significantly steered by the con-centration of Na_(2)CO_(3).Scanning electron microscopy analysis demonstrated that the intro-duction of Na_(2)CO_(3)into cellulose at an appropriate concentration led to the formation of tubular structure on its surface after pyrolysis,whereas the tubular structure was absent in the lignin char with the addition of Na_(2)CO_(3)at any concentrations.X-ray diffraction and Ra-man spectroscopy characterizations revealed that all the obtained chars from both cellulose and lignin,with or without Na_(2)CO_(3),were ascribed to non-crystalline graphite.Nevertheless,the crystal orientation of graphite from cellulose and lignin changed after the catalysis of Na_(2)CO_(3).Further electrochemical tests showed that cellulose char had a higher sodium stor-age capacity than that of lignin char.The excellent electrochemical performance of carbon materials derived from cellulose might hold a prospective application in the field of energy storage.
基金financially supported by the National Natural Science Foundation of China(21808242)the Shandong Provincial Natural Science Foundation(ZR2018BB070)+1 种基金the Fundamental Research Funds for the Central Universities of China(19CX02042A)the Foundation of State Key Laboratory of Highefficiency Utilization of Coal and Green Chemical Engineering(2020-KF-31)。
文摘Developing of economic and efficient catalysts is critical for the application of electroreduction of carbon dioxide to highly valuable chemicals.Herein,we present a facile method to synthesize N-doped hieratically porous carbon through pyrolysis of petroleum pitch followed by ammonia etching.We found mesopores are favored formation by removing of asphaltene from petroleum pitch during the carbonation process.Simultaneously,ammonia etching can not only increase the pyridinic-N content,but also upgrade the ratio of meso-to micro-pores of carbon materials.Using the N-doped hieratically porous carbon as catalyst for carbon dioxide electroreduction,the Faradaic efficiency of carbon monoxide reaches 83%at-0.9 V vs.the reversible hydrogen electrode(RHE)in 0.1 M KHCO_(3).This superior performance is attributed to the synergistic effects of highly pyridinic-N content in conjunction with the hieratically porous architecture,rendering abundant exposed and accessible active sites for electroreduction of CO_(2).Our work provides a new strategy for the large-scale preparation of high-performance,low-cost catalysts for CO_(2) electroreduction.
