Sulfonated aromatic copoly(ether-amide) membranes II: Influence of chain length and sulfonic groups concentration on membrane ionic conductivity and mechanical properties

被引:4
作者
Elim Sosa-Gonzalez, Wadi [1 ]
del Jesus Pali-Casanova, Ramon [2 ]
Perez-Padilla, Yamile [3 ]
Isabel Loria-Bastarrachea, Maria [4 ]
Luis Santiago-Garcia, Jose [4 ]
de Jesus Aguilar-Vega, Manuel [4 ]
机构
[1] Inst Tecnol Super Champoton, Carretera Champoton Isla Aguada Km, Champoton, Campeche, Mexico
[2] Inst Tecnol Super Los Rios, Tabasco, Mexico
[3] Univ Autonoma Yucatan, Fac Ingn Quim, Merida, Yucatan, Mexico
[4] Ctr Invest Cient Yucatan AC, Lab Membranas, Unidad Mat, Calle 43 130, Merida 97200, Yucatan, Mexico
关键词
Sulfonated copoly(ether-amide)s; proton exchange membranes; mechanical properties; poly(ether-amide); sulfonated aramides; ion exchange capacity; PROTON-EXCHANGE MEMBRANE; FUEL-CELL APPLICATION; ETHER KETONE KETONE); ISOPHTHALIC COPOLYAMIDES; GAS-PERMEABILITY; WATER STABILITY; POLYAMIDES; POLYIMIDES; ACID; POLYELECTROLYTES;
D O I
10.1177/0954008317699863
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
Several aromatic sulfonated copoly(ether-amide)s, based on the aromatic diamines 4,4-(hexafluoroisopropylidene)bis(p-phenyleneoxy)-dianiline (HFD) and 2,4-diaminobenzensulfonic acid (DABS) and 4,4-oxybis(benzoic acid) (OBA), were synthesized through a polycondensation reaction. The sulfonation degree was controlled by introducing different concentrations of 2,4-DABS from 40 mol% up to 80 mol%. Proton nuclear magnetic resonance validated the expected concentrations of sulfonic acid groups in the sulfonated aromatic copoly(ether-amide)s. Thermal decomposition of sulfonic groups was found to initiate at 280 degrees C, while main chain decomposition initiates at 410 degrees C. Proton conductivity between 30 degrees C and 75 degrees C was 19.0 and 45.0 mS/cm, respectively, for the copolymer with the highest concentration of sulfonic groups (-SO3H). Comparison with structurally similar sulfonated copolyamides and copoly(ether-amide)s indicates that these new sulfonated copoly(ether-amide)s based on 4,4-OBA show improved mechanical properties, but a decrease in ion exchange capacity and proton conductivity.
引用
收藏
页码:437 / 445
页数:9
相关论文
共 54 条
  • [11] Gas permeability and selectivity of benzophenone aromatic isophthalic copolyamides
    Carrera-Figueiras, Cristian
    Aguilar-Vega, Manuel
    [J]. JOURNAL OF POLYMER SCIENCE PART B-POLYMER PHYSICS, 2007, 45 (15) : 2083 - 2096
  • [12] Carrette L, 2001, FUEL CELLS, V1, P5, DOI 10.1002/1615-6854(200105)1:1<5::AID-FUCE5>3.0.CO
  • [13] 2-G
  • [14] Partially Fluorinated Sulfonated Poly(ether amide) Fuel Cell Membranes: Influence of Chemical Structure on Membrane Properties
    Chang, Ying
    Lee, Yeong-Beom
    Bae, Chulsung
    [J]. POLYMERS, 2011, 3 (01): : 222 - 235
  • [15] Development and characterization of ion-exchange polymer blend membranes
    Cui, W
    Kerres, J
    Eigenberger, G
    [J]. SEPARATION AND PURIFICATION TECHNOLOGY, 1998, 14 (1-3) : 145 - 154
  • [16] Proton-Conducting Polymer Electrolyte Membranes: Water and Structure in Charge
    Eikerling, Michael
    Kornyshev, Alexei A.
    Spohr, Eckhard
    [J]. FUEL CELLS I, 2008, 215 : 15 - 54
  • [17] New polyamides containing azobenzene unites and hydantoin derivatives in main chain: synthesis and characterization
    Faghihi, K
    Hagibeygi, M
    [J]. EUROPEAN POLYMER JOURNAL, 2003, 39 (12) : 2307 - 2314
  • [18] Novel sulfonated polyimides as polyelectrolytes for fuel cell application.: 1.: Synthesis, proton conductivity, and water stability of polyimides from 4,4′-diaminodiphenyl ether-2,2′-disulfonic acid
    Fang, JH
    Guo, XX
    Harada, S
    Watari, T
    Tanaka, K
    Kita, H
    Okamoto, K
    [J]. MACROMOLECULES, 2002, 35 (24) : 9022 - 9028
  • [19] Gabrielli C., 1984, IDENTIFICATION ELECT, P130
  • [20] Synthesis and characterization of poly(ether sulfone) grafted poly(styrene sulfonic acid) for proton conducting membranes
    Goh, Yoon Taik
    Patel, Rajkumar
    Im, Se Jun
    Kim, Jong Hak
    Min, Byoung Ryul
    [J]. KOREAN JOURNAL OF CHEMICAL ENGINEERING, 2009, 26 (02) : 518 - 522