Dual physically crosslinked double network hydrogels with high toughness and self-healing properties.
نویسندگان
چکیده
Toughness and self-healing properties are desirable characteristics in engineered hydrogels used for many practical applications. However, it is still challenging to develop hydrogels exhibiting both of these attractive properties in a single material. In this work, we present the fabrication of fully physically-linked Agar/PAAc-Fe3+ DN gels. These hydrogels exhibited dual physical crosslinking through a hydrogen bonded crosslinked agar network firstly, and a physically linked PAAc-Fe3+ network via Fe3+ coordination interactions secondly. Due to this dual physical crosslinking, the fabricated Agar/PAAc-Fe3+ DN gels exhibited very favorable mechanical properties (tensile strength 320.7 kPa, work of extension 1520.2 kJ m-3, elongation at break 1130%), fast self-recovery properties in Fe3+ solution (100% recovery within 30 min), in 50 °C conditions (100% recovery within 15 min), and under ambient conditions (100% recovery of the initial properties within 60 min), as well as impressive self-healing properties under ambient conditions. All of the data indicate that both the hydrogen bonds in the first network and the ionic coordination interactions in the second network act as reversible sacrificial bonds to dissipate energy, thus conferring high mechanical and recovery properties to the prepared Agar/PAAc-Fe3+ DN gels.
منابع مشابه
Engineering mechanical dissipation in solid poly ( ethylene glycol ) hydrogels
Growing evidence supports that the unique mechanical behavior of mussel byssal threads, such as high toughness and self-healing, rely on an intricate balance of permanent covalent and reversible metal coordination bonds. Inspired by this material crosslink chemistry balance, we synthesized polyethylene glycol (PEG) hydrogels with two crosslinked networks; a primary permanent network composed of...
متن کاملAcrylamide Polymer Double-Network Hydrogels
Background: In focal repair of joint cartilage and meniscus, initial stiffness and strength of repairs are generally much less than surrounding tissue. This increases early failure potential. Secure primary fixation of the repair material is also a problem. Acrylamide polymer double-network (DN) hydrogels are candidate-improved repair materials. DN gels have exceptional strength and toughness c...
متن کاملInvestigation of synthesis of PVP hydrogel by irradiation
Background: A dressing often covers the wound to accelerate its healing. Hydrocolloid-type dressing to give better conditions for healing has been developed consisting of gelatin, pectin, water and hydrophilic polymer which promote healing. In recent years, much attention has been focused on the research and development of polymer hydrogels as biomaterials, such as contact lenses, wound dressin...
متن کاملSelf-healing hydrogels containing reversible oxime crosslinks.
Self-healing oxime-functional hydrogels have been developed that undergo a reversible gel-to-sol transition via oxime exchange under acidic conditions. Keto-functional copolymers were prepared by conventional radical polymerization of N,N-dimethylacrylamide (DMA) and diacetone acrylamide (DAA). The resulting water soluble copolymers (P(DMA-stat-DAA)) were chemically crosslinked with difunctiona...
متن کاملTransparent crosslinked ultrashort peptide hydrogel dressing with high shape-fidelity accelerates healing of full-thickness excision wounds
Wound healing is a major burden of healthcare systems worldwide and hydrogel dressings offer a moist environment conducive to healing. We describe cysteine-containing ultrashort peptides that self-assemble spontaneously into hydrogels. After disulfide crosslinking, the optically-transparent hydrogels became significantly stiffer and exhibited high shape fidelity. The peptide sequence (LIVAGKC o...
متن کاملذخیره در منابع من
با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید
برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید
ثبت ناماگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید
ورودعنوان ژورنال:
- Soft matter
دوره 13 5 شماره
صفحات -
تاریخ انتشار 2017