Why are double network hydrogels so tough

Double-network (DN) gels have drawn much attention as an innovative material having both high water content (ca. 90 wt%) and high mechanical strength and toughness. DN gels are characterized by a special network structure consisting of two types of polymer components with opposite physical natures: the minor component is abundantly cross-linked polyelectrolytes (rigid skeleton) and the major component comprises of poorly cross-linked neutral polymers (ductile substance). The former and the latter components are referred to as the first network and the second network, respectively, since the synthesis should be done in this order to realize high mechanical strength. For DN gels synthesized under suitable conditions (choice of polymers, feed compositions, atmosphere for reaction, etc.), they possess hardness (elastic modulus of 0.1–1.0 MPa), strength (failure tensile nominal stress 1–10 MPa, strain 1000–2000%; failure compressive nominal stress 20–60 MPa, strain 90–95%), and toughness (tearing fracture energy of 100∼1000 J m−2). These excellent mechanical performances are comparable to that of rubbers and soft load-bearing bio-tissues. The mechanical behaviors of DN gels are inconsistent with general mechanisms that enhance the toughness of soft polymeric materials. Thus, DN gels present an interesting and challenging problem in polymer mechanics. Extensive experimental and theoretical studies have shown that the toughening of DN gel is based on a local yielding mechanism, which has some common features with other brittle and ductile nano-composite materials, such as bones and dentins.

[1]  A. Oloyede,et al.  Conceptual fracture parameters for articular cartilage. , 2007, Clinical biomechanics.

[2]  Toshihiro Hirai,et al.  Actuation of Poly(vinyl alcohol) Gel by Electric Field , 1993 .

[3]  T. Kurokawa,et al.  Effect of polymer entanglement on the toughening of double network hydrogels. , 2005, The journal of physical chemistry. B.

[4]  J. Gong,et al.  The molecular origin of enhanced toughness in double-network hydrogels: A neutron scattering study☆ , 2007 .

[5]  J. Gong,et al.  Necking Phenomenon of Double-Network Gels , 2006 .

[6]  Hidemitsu Furukawa,et al.  Swelling-induced modulation of static and dynamic fluctuations in polyacrylamide gels observed by scanning microscopic light scattering. , 2003, Physical review. E, Statistical, nonlinear, and soft matter physics.

[7]  Yoshimi Tanaka,et al.  Importance of entanglement between first and second components in high-strength double network gels , 2007 .

[8]  Yoshihito Osada,et al.  Cultivation of endothelial cells on adhesive protein-free synthetic polymer gels. , 2005, Biomaterials.

[9]  J. Gong,et al.  Large Strain Hysteresis and Mullins Effect of Tough Double-Network Hydrogels , 2007 .

[10]  J. Hedrick,et al.  Synthesis of well-defined hydrogel networks using click chemistry. , 2006, Chemical communications.

[11]  Huajian Gao,et al.  A study of fracture mechanisms in biological nano-composites via the virtual internal bond model , 2004 .

[12]  Xiaobo Hu,et al.  Network chain density and relaxation of in situ synthesized polyacrylamide/hectorite clay nanocomposite hydrogels with ultrahigh tensibility , 2008 .

[13]  H. Brown A Model of the Fracture of Double Network Gels , 2007 .

[14]  Brittle, ductile, paste-like behaviors and distinct necking of double network gels with enhanced heterogeneity , 2009 .

[15]  Fracture energy of gels , 2000, cond-mat/0003474.

[16]  J. Gong,et al.  Thermodynamic interactions in double-network hydrogels. , 2008, The journal of physical chemistry. B.

[17]  Bonn,et al.  Delayed fracture of an inhomogeneous soft solid , 1998, Science.

[18]  Yoshihito Osada,et al.  ELECTRICALLY ACTIVATED MECHANOCHEMICAL DEVICES USING POLYELECTROLYTE GELS , 1985 .

[19]  K. Okumura,et al.  Toughness of double elastic networks , 2004 .

[20]  Yoshihito Osada,et al.  Soft and Wet Materials: Polymer Gels , 1998 .

[21]  A. Metters,et al.  Hydrogels in controlled release formulations: network design and mathematical modeling. , 2006, Advanced drug delivery reviews.

[22]  Y. Tanaka,et al.  A local damage model for anomalous high toughness of double-network gels , 2007 .

[23]  M R Wisnom,et al.  The compressive strength of articular cartilage , 1998, Proceedings of the Institution of Mechanical Engineers. Part H, Journal of engineering in medicine.

[24]  P. Calvert Hydrogels for Soft Machines , 2009 .

[25]  Yoshimi Tanaka,et al.  True Chemical Structure of Double Network Hydrogels , 2009 .

[26]  P. de Gennes,et al.  Why is nacre strong? Elastic theory and fracture mechanics for biocomposites with stratified structures , 2001 .

[27]  T. Kurokawa,et al.  Double‐Network Hydrogels with Extremely High Mechanical Strength , 2003 .

[28]  K. Ito,et al.  The Polyrotaxane Gel: A Topological Gel by Figure‐of‐Eight Cross‐links , 2001 .

[29]  T. Okano,et al.  Comb-type grafted hydrogels with rapid deswelling response to temperature changes , 1995, Nature.

[30]  Jian Ping Gong,et al.  Friction and lubrication of hydrogels-its richness and complexity. , 2006, Soft matter.

[31]  Toru Takehisa,et al.  Nanocomposite Hydrogels: A Unique Organic–Inorganic Network Structure with Extraordinary Mechanical, Optical, and Swelling/De‐swelling Properties , 2002 .

[32]  T. Kurokawa,et al.  A novel double-network hydrogel induces spontaneous articular cartilage regeneration in vivo in a large osteochondral defect. , 2009, Macromolecular bioscience.

[33]  Y. Osada,et al.  A polymer gel with electrically driven motility , 1992, Nature.

[34]  J. Gong,et al.  In vitro differentiation of chondrogenic ATDC5 cells is enhanced by culturing on synthetic hydrogels with various charge densities. , 2010, Acta biomaterialia.

[35]  Fracture and adhesion of elastomers and gels: Large strains at small length scales , 2006 .

[36]  Won-Gun Koh,et al.  Biomimetic strain hardening in interpenetrating polymer network hydrogels , 2007 .

[37]  P. Gennes,et al.  Rubber-rubber adhesion with connector molecules , 1992 .

[38]  H. Brown A molecular interpretation of the toughness of glassy polymers , 1991 .

[39]  A. Thomas,et al.  The strength of highly elastic materials , 1967, Proceedings of the Royal Society of London. Series A. Mathematical and Physical Sciences.

[40]  Yoshihito Osada,et al.  High Mechanical Strength Double‐Network Hydrogel with Bacterial Cellulose , 2004 .

[41]  Huan Li,et al.  Mechanical Properties and Structure of Polymer−Clay Nanocomposite Gels with High Clay Content , 2006 .

[42]  Kohzo Ito,et al.  Novel Cross-Linking Concept of Polymer Network: Synthesis, Structure, and Properties of Slide-Ring Gels with Freely Movable Junctions , 2007 .

[43]  Yoshihito Osada,et al.  Structural Characteristics of Double Network Gels with Extremely High Mechanical Strength , 2004 .

[44]  J. Gong,et al.  Dynamic cell behavior on synthetic hydrogels with different charge densities , 2009 .

[45]  T. Kurokawa,et al.  Determination of fracture energy of high strength double network hydrogels. , 2005, The journal of physical chemistry. B.

[46]  Yuji Yamamoto,et al.  Design and Fabrication of a High-Strength Hydrogel with Ideally Homogeneous Network Structure from Tetrahedron-like Macromonomers , 2008 .

[47]  J. Gong,et al.  Effect of Aspect Ratio on Protein Diffusion in Hydrogels , 2000 .

[48]  L. Leibler,et al.  Large-scale heterogeneities in randomly cross-linked networks , 1988 .

[49]  Tanaka,et al.  Critical kinetics of volume phase transition of gels. , 1985, Physical review letters.

[50]  W. Goddard,et al.  Mechanical and transport properties of the poly(ethylene oxide)-poly(acrylic acid) double network hydrogel from molecular dynamic simulations. , 2007, The journal of physical chemistry. B.

[51]  R O Ritchie,et al.  Crack blunting, crack bridging and resistance-curve fracture mechanics in dentin: effect of hydration. , 2003, Biomaterials.

[52]  Critical stress intensity factors of wet gels , 1988 .

[53]  Jacqueline A. Cutroni,et al.  Sacrificial bonds and hidden length dissipate energy as mineralized fibrils separate during bone fracture , 2005, Nature materials.

[54]  Andrew Gouldstone,et al.  Mechanically strong double network photocrosslinked hydrogels from N,N-dimethylacrylamide and glycidyl methacrylated hyaluronan. , 2008, Biomaterials.

[55]  Effects of chain pull-out on adhesion of elastomers , 1993 .

[56]  T. Kurokawa,et al.  Localized Yielding Around Crack Tips of Double-Network Gels , 2008 .

[57]  R. Wool Self-healing materials: a review. , 2008, Soft matter.

[58]  B. Pogue,et al.  Review of tissue simulating phantoms for optical spectroscopy, imaging and dosimetry. , 2006, Journal of biomedical optics.

[59]  T. Kurokawa,et al.  Ultrathin tough double network hydrogels showing adjustable muscle-like isometric force generation triggered by solvent. , 2009, Chemical communications.

[60]  K Burczak,et al.  Long-term in vivo performance and biocompatibility of poly(vinyl alcohol) hydrogel macrocapsules for hybrid-type artificial pancreas. , 1996, Biomaterials.

[61]  D. Scharp,et al.  Islet immuno-isolation: The use of hybrid artificial organs to prevent islet tissue rejection , 1984, World Journal of Surgery.

[62]  Allan S Hoffman,et al.  Hydrogels for biomedical applications. , 2002, Advanced drug delivery reviews.

[63]  Masaru Yoshida,et al.  High-water-content mouldable hydrogels by mixing clay and a dendritic molecular binder , 2010, Nature.

[64]  J. Gong,et al.  Molecular model for toughening in double-network hydrogels. , 2008, The journal of physical chemistry. B.

[65]  T. Kurokawa,et al.  Direct Observation of Damage Zone around Crack Tips in Double-Network Gels , 2009 .