Tough and Thermosensitive Poly(N-isopropylacrylamide)/Graphene Oxide Hydrogels with Macroscopically Oriented Liquid Crystalline Structures.
نویسندگان
چکیده
Bulk graphene oxide (GO) nanocomposite materials with macroscopically oriented GO liquid crystalline (LC) structures exhibit interesting anisotropic properties, but their facile preparations remain challenging. This work reports for the first time the facile preparation of poly(N-isopropylacrylamide) (PNIPAM)/GO nanocomposite hydrogels with macroscopically oriented LC structures with the assistance of a flow field induced by vacuum degassing and the in situ polymerization accelerated by GO. The hydrogel prepared with a GO concentration of 5.0 mg mL(-1) exhibits macroscopically aligned LC structures, which endow the gels with anisotropic optical, mechanical properties, and dimensional changes during the phase transition. The hydrogels show dramatically enhanced tensile mechanical properties and phase transition rates. The oriented LC structures are not damaged during the phase transition of the PNIPAM/GO hydrogels, and hence their LC behavior undergoes reversible change. Moreover, highly oriented LC structures can also be formed when the gels are elongated, even for the gels which do not have macroscopically oriented LC structures. Very impressively, the oriented LC structures in the hydrogels can be permanently maintained by drying the gel samples elongated to and then kept at a constant tensile strain. The thermosensitive nature of PNIPAM and the angle-dependent nature of the macroscopically aligned GO LC structures allow the practical applications of the PNIPAM/GO hydrogels as optical switches, soft sensors, and actuators and so on.
منابع مشابه
Effect of the initiator on thermosensitive rate of poly(N-isopropylacrylamide) hydrogels
As the main of thermosensitive polymeric materials, poly(N-isopropylacrylamide) (PNIPAM) undergoes volume changes in response to external temperature changes. While in some potential applications, a fast response rate is needed. In this article, effect of the initiator on thermosensitivity of PNIPAM hydrogels was carried out. The characterization of the resulting hydrogels was gravimetrically m...
متن کاملIn situ-forming hydrogels--review of temperature-sensitive systems.
In the past few years, an increasing number of in situ-forming systems have been reported in the literature for various biomedical applications, including drug delivery, cell encapsulation, and tissue repair. There are several possible mechanisms that lead to in situ gel formation: solvent exchange, UV-irradiation, ionic cross-linkage, pH change, and temperature modulation. The thermosensitive ...
متن کاملGraphene-containing thermoresponsive nanocomposite hydrogels of poly(N-isopropylacrylamide) prepared by frontal polymerization
Frontal polymerization has been successfully used to synthesize poly(N-isopropylacrylamide) nanocomposite hydrogels containing graphene. The latter was directly achieved by ultrasound treatment of a dispersion of graphite inN-methylpyrrolidone. The dispersion, having the concentration of 2.21 g L , was characterized by TEM analysis and mixed with suitable amounts of N-isopropylacrylamide for th...
متن کاملDual Nano-Carriers using Polylactide-block-Poly(N-isopropylacrylamide-random-acrylic acid) Polymerized from Reduced Graphene Oxide Surface for Doxorubicin Delivery Applications
The stimuli-responsive nanocomposites were designed as drug delivery nanocarriers. Thanks to promising properties such as large surface area and easy chemical functionalization, the graphene derivatives can be used for the drug delivery applications. For this purpose, in the current work, the poly(L,D-lactide)-block-poly(N-isopropylacrylamide-rand-acrylic acid) grafted from reduced graphene oxi...
متن کاملAn infrared-light responsive graphene-oxide incorporated poly(N-isopropylacrylamide) hydrogel nanocomposite
We demonstrate a new light-responsive poly(N-isopropylacrylamide) (PNIPAAm) hydrogel nanocomposite incorporating glycidyl methacrylate functionalized graphene oxide (GO–GMA) instead of metallic nanoparticle fillers. GO–GMA is synthesized by esterification with glycidyl methacrylate. GO–GMA incorporated hydrogels are synthesized by photopolymerization of NIPAAm including 4-dimethylaminopyridine ...
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:
- ACS applied materials & interfaces
دوره 8 24 شماره
صفحات -
تاریخ انتشار 2016