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Hydrogels with high mechanical strength, good crack resistance, and good adhesion are highly desirable in various areas, such as soft electronics and wound dressing. Yet, these properties are usually mutually exclusive, so achieving such hydrogels is difficult. Herein, we fabricate a series of strong, tough, and adhesive composite hydrogels from polyampholyte (PA) gel reinforced by nonwoven cellulose-based fiber fabric (CF) via a simple composite strategy. In this strategy, CF could form a good interface with the relatively tough PA gel matrix, providing high load-bearing capability and good crack resistance for the composite gels. The relatively soft, sticky PA gel matrix could also provide a large effective contact area to achieve good adhesion. The effect of CF content on the mechanical and adhesion properties of composite gels is systematically studied. The optimized composite gel possesses 35.2 MPa of Young's modulus, 4.3 MPa of tensile strength, 8.1 kJ m−2 of tearing energy, 943 kPa of self-adhesive strength, and 1.4 kJ m−2 of self-adhesive energy, which is 22.1, 2.3, 1.8, 6.0, and 4.2 times those of the gel matrix, respectively. The samples could also form good adhesion to diverse substrates. This work opens a simple route for fabricating strong, tough, and adhesive hydrogels. [ABSTRACT FROM AUTHOR]

The adhesion strength and water resistance of stainless steel and adhesive resin composites determine the long‐term performance of wires and cables; however, adhesion at stainless steel interfaces is difficult. Herein, we prepared ethylene acrylic acid/linear low‐density polyethylene (EAA/LLDPE) blends with good mechanical and adhesive properties. Silane was anchored to the surface of stainless steel. The effects of silane functionalization on the adhesion surface were investigated by X‐ray photoelectron spectroscopy and Fourier transform infrared spectroscopy. The reaction mechanism between the stainless steel, silane, and EAA/LLDPE revealed adhesion was optimized when a 3:7 volume ratio of 3‐methacryloxypropyltrimethoxysilane (MEMO): 3‐aminopropyltrimethoxysilane (A‐1110) was used to modify the stainless steel substrate. SEM images of EAA/LLDPE film peel surfaces found the silane‐treated stainless steel substrates produced rough surfaces with a uniform void indicating the silane treatment enhanced the stainless steel and EAA/LLDPE film interaction. The stainless steel and EAA/LLDPE film adhesion and water resistance improved and the peel strength after water resistance testing at 68°C for 168 h increased from 3.18 N/cm to 9.37 N/cm compared to untreated stainless steel. Silane‐modified stainless steel and EAA/LLDPE blend film composite materials demonstrate potential for application in wires and cables used in environmental corrosion‐resistant applications. POLYM. ENG. SCI., 59:1866–1873, 2019. © 2019 Society of Plastics Engineers [ABSTRACT FROM AUTHOR]

Polyampholyte (PA) hydrogels in general possess excellent mechanical properties, but their underwater applications are largely limited due to swelling induced dramatically reduced strength and poor wet adhesion, especially in high salinity environments. Here, we report our approach to fabricating an anti-swelling poly(acryloyloxyethyltrimethyl ammonium chloride (DAC) -co- sodium p-styrenesulfonate (NaSS) -co- 2-Vinyl-4,6-diamino-1,3,5-triazine (VDT), or P(DAC -co- NaSS -co- VDT), PA hydrogel by introducing multi-hydrogen bonding capable functional VDT moieties into the DAC/NaSS coexisting and cation/anion ratio easily tunable PA network. The mechanical properties of the P(DAC -co- NaSS -co- VDT) hydrogel in bulk and at interface were controllable with dimethyl sulfoxide (DMSO)/H 2 O solvent displacement and Hofmeister effect in a wide salinity range, exhibiting maximum tensile strength, Young's modulus, and wet adhesion toughness of 7.6 MPa, 200 MPa, and 350 J m−2, respectively. The anti-swelling and strong P(DAC -co- NaSS -co- VDT) PA hydrogel developed in this work may find great potential in underwater sensing and sewage treatment as well as for many biomedical applications. • Polyelectrolyte P(DAC -co- NaSS -co- VDT) hydrogels can maintain volume stability in different salt solutions. • Hofmeister effect improves the mechanical properties of hydrogels. • The underwater adhesion of hydrogel can be regulated by solvent exchange. [ABSTRACT FROM AUTHOR]

Naturally occurring polysaccharide-based polyelectrolyte complex (PEC) physical hydrogels have broad applications in biomedicine. Yet, obtaining high-strength, strong-adhesion, and antibacterial PEC hydrogels via physically crosslinking of natural polysaccharides still remains a challenge. In this work, a chitosan (CS)/sodium alginate (SA) PEC physical hydrogel film was developed by using two oppositely charged natural polysaccharides, CS and SA, of equivalently high molecular weight (M w , approx. 105 Da), the tensile stress of which was achieved as high as 12.3 MPa due to CS-CS intermolecular hydrogen bonding and CS-SA electrostatic interaction. In addition, the hydrogel films, upon protonation at acidic conditions (e.g. pH 2.6), exhibited excellent antibacterial activity against Escherichia coli (E. coli) and the CS/SA hydrogel films also demonstrated strong adhesion to biological tissue. The high M w -matching, two-component natural polysaccharide approach presented in this work to preparing high-strength, strong-adhesion, and antibacterial PEC hydrogels may shed some lights on converting renewable biomass to value-added biomaterials. The hydrogel films (CS/SA) prepared by self-assembly of chitosan (CS) and sodium alginate (SA) with high molecular weight have a large number of hydrogen bonds and electrostatic interactions, the synergistic effect of those two makes the hydrogel have excellent mechanical properties. This hydrogel films also have strong tissue adhesion and bacteriostatic properties, with which the hydrogel films could be used for converting renewable biomass to value-added biomaterials. [Display omitted] • The hydrogen bonds and electrostatic interactions of CS/SA gel made it have excellent mechanical properties. • Ag+ made the CS/SA hydrogel films exhibited excellent mechanical properties and antibacterial activity. • The CS/SA hydrogels demonstrated excellent adhesion to biological tissues and promptly closed a wound. [ABSTRACT FROM AUTHOR]

Hydrogels that possess adequate toughness in bulk and at soft interface are highly desirable. We report a fully physically crosslinked dual Amylopectin (Amy, the first network)/poly(N-hydroxyethyl acrylamide) (PHEAA, the second network) hydrogel, where both networks were hydrogen bonding (H-bonding) crosslinked, with super toughness in bulk and tunable adhesion at hydrogel-soft tissue interface. Through adjustment of hydrogen bond density, strong and tough hydrogels were prepared that exhibited different levels of adhesion strength and three adhesive failure mechanisms. We replaced Amy with oxidized starch (OSA) to synthesize dual and hybrid chemically/physically crosslinked OSA/PHEAA double network (DN) hydrogels that were capable of forming Schiff's bases at hydrogel-hydrogel or hydrogel-tissue interfaces, aside from interfacial H-bonding, incurring sustained, high interfacial toughness (1850 J m−2 hydrogel-hydrogel and 610 J m−2 hydrogel-tissue) in wet environments. Such tough and adhesive DN hydrogels have great potential in various applications such as engineering of artificial soft tissues or implantable devices that are intended to adhere to internal organs or tissues. • Fully physically crosslinked hydrogels via H-bonding. • Tunable adhesion and three adhesive failure mechanisms of hydrogels. • The sacrificial bonds including H-bonds and reversible Schiff's bases at the interface. • High interfacial toughness at hydrogel-hydrogel or hydrogel-tissue interfaces in wet environments. [ABSTRACT FROM AUTHOR]