Tough interpenetrating Pluronic F127/polyacrylic acid hydrogels

被引:37
作者
Baskan, Tuba [1 ]
Tuncaboylu, Deniz C. [2 ]
Okay, Oguz [1 ]
机构
[1] Istanbul Tech Univ, Dept Chem, TR-34469 Istanbul, Turkey
[2] Bezmialem Vakif Univ, Fac Pharm, TR-34093 Istanbul, Turkey
关键词
Hydrogels; Toughness; Hydrophobic associations; DOUBLE-NETWORK HYDROGELS; SELF-HEALING HYDROGELS; TRIBLOCK COPOLYMER; DRUG-DELIVERY; AGGREGATION BEHAVIOR; POLY(ACRYLIC ACID); AQUEOUS-SOLUTIONS; POLYELECTROLYTE; MICROGELS; DYNAMICS;
D O I
10.1016/j.polymer.2013.03.066
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
Tough interpenetrating polymer network (IPN) hydrogels with pH- and temperature sensitivity were prepared by crosslinking copolymerization of acrylic acid (AAc) and N,N'-methylenebis(acrylamide) in 20 w/v% aqueous solutions of F127 (PEO99-PPO65-PEO99). The presence of F127 within the gel network slightly decreases the elastic modulus while the loss factor significantly increases, revealing increasing energy dissipation in IPN hydrogels. Cyclic compression tests show large mechanical hysteresis in IPN hydrogels due to the reversible formation of ionic clusters and hydrophobic associations of F127 molecules. The dissipative mechanisms created by F127 lead to the improvement in the mechanical performance of IPN hydrogels when compared to the polyacrylic acid (PAAc) gel controls. PAAc hydrogel formed at 10% AAc fractures under a compression of 0.2 MPa at 78% strain, while the corresponding IPN hydrogel sustains up to 7 MPa compressions at 98% strain, leading to an increase of toughness from 31 to 335 kJ/m(3). IPN hydrogels subjected to the heating-cooling cycles between below and above the micellization temperature of F127 show characteristic features of F127 solutions, i.e., increase of the dynamic moduli on raising the temperature, and thermal hysteresis behavior. (c) 2013 Elsevier Ltd. All rights reserved.
引用
收藏
页码:2979 / 2987
页数:9
相关论文
共 43 条
  • [31] CYCLIZATION AND REDUCED PENDANT VINYL GROUP REACTIVITY DURING THE FREE-RADICAL CROSS-LINKING POLYMERIZATION OF 1,4-DIVINYLBENZENE
    OKAY, O
    KURZ, M
    LUTZ, K
    FUNKE, W
    [J]. MACROMOLECULES, 1995, 28 (08) : 2728 - 2737
  • [32] Structure and rheology studies of poly(oxyethylene-oxypropylene-oxyethylene) aqueous solution
    Prudhomme, RK
    Wu, GW
    Schneider, DK
    [J]. LANGMUIR, 1996, 12 (20) : 4651 - 4659
  • [33] Stabilization of pluronic P-105 micelles with an interpenetrating network of N,N-diethylacrylamide
    Pruitt, JD
    Husseini, G
    Rapoport, N
    Pitt, MG
    [J]. MACROMOLECULES, 2000, 33 (25) : 9306 - 9309
  • [34] Ethoxysilane-capped PEO-PPO-PEO triblocks: a new family of reverse thereto-responsive polymers
    Sosnik, A
    Cohn, D
    [J]. BIOMATERIALS, 2004, 25 (14) : 2851 - 2858
  • [35] STAFFORD JW, 1970, MAKROMOLEKUL CHEM, V134, P71
  • [36] Rheological Behavior of Responsive DNA Hydrogels
    Topuz, Fuat
    Okay, Oguz
    [J]. MACROMOLECULES, 2008, 41 (22) : 8847 - 8854
  • [37] Treloar RG., 1975, PHYS RUBBER ELASTICI, V3
  • [38] Structure optimization of self-healing hydrogels formed via hydrophobic interactions
    Tuncaboylu, Deniz C.
    Argun, Aslihan
    Sahin, Melahat
    Sari, Murat
    Okay, Oguz
    [J]. POLYMER, 2012, 53 (24) : 5513 - 5522
  • [39] Dynamics and Large Strain Behavior of Self-Healing Hydrogels with and without Surfactants
    Tuncaboylu, Deniz C.
    Sahin, Melahat
    Argun, Aslihan
    Oppermann, Wilhelm
    Okay, Oguz
    [J]. MACROMOLECULES, 2012, 45 (04) : 1991 - 2000
  • [40] Associating behaviour of polyacrylamides hydrophobically modified with dihexylacrylamide
    Volpert, E
    Selb, J
    Candau, F
    [J]. POLYMER, 1998, 39 (05) : 1025 - 1033