Synthesis and characterization of inherently radiopaque nanocomposites using biocompatible iodinated poly(methyl methacrylate-co-acrylamide) and graphene oxide (original) (raw)
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Journal of Polymer Research
New radiopaque nanocomposites were prepared using iodinated copolymers and cloisite 20A, as reinforcement agent. Iodinated copolymers were prepared through copolymerization of Methyl methacrylate and acrylic acid and subsequently modification of the P(MMA-co-AA) via 4iodophenyl isocynate and 3,4,5-triiophenyl isocyanate for synthesis of 1I-P(MMA-co-AA) and 3I-P(MMA-co-AA) respectively. Preparation of the nanocomposites was carried out by the solution method using various amounts of organoclay. In order to investigate the effect of iodinated substituents on the morphology and thermal characteristics of the composite samples, the P(MMA-co-AA) was modified via phenyl isocyanate (PIC-P(MMA-co-AA)) and then the nanocomposites were prepared using cloisite 20A. All the nanocomposite samples were characterized by X-ray diffraction (XRD), scanning electron microscopoy (SEM), and thermogravimetric analysis (TGA). The X-ray visibility of the radiopaque nanocomposites was also explored using X-radiography. The results obtained indicated that the iodinated nanocomposites had an excellent radiopacity, and due to their biocompatibility, they could be used for medical applications.
Journal of Materials Science
New radiopaque nanocomposites were prepared based on iodinated polyurethane-urea (PUU) and graphene oxide (GO). The iodinated PUU was synthesized using 4,4 0-methylenediphenyl diisocyanate (MDI), polyethylene glycol (PEG, Mn = 1000), and 4-(4-iodophenyl)-1,2,4-triazolidine-3,5-dione (IUr) as a novel chain extender and radiopacifying agent. The synthesized urazole, PUU, and the related nanocomposites are characterized by fourier transform infrared spectrum, nuclear magnetic resonance, X-ray diffraction, field-emission scanning electron microscopy, elemental analysis (CHNO), thermogravimetric analysis, and dynamic mechanical thermal analysis (DMTA). The X-ray visibility of the radiopaque PUU and nanocomposites was investigated using X-radiography. To evaluate the biocompatibility of the samples, the indirect MTT [3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide] assay was carried out on the non-cancerous mouse fibroblast cell line NIH3T3 D4 according to the ISO10993-5 standard. The DMTA results proved introduction of the GO layers into the iodinated PUU matrix, and has improved mechanical properties of the nanocomposites compared to the pure polymer. The X-ray images showed significant radiopacity of the pure polymer and the nanocomposites.
Journal of Nanotechnology, 2016
We describe the synthesis of acid functionalized graphene (GE) which is grafted to chitosan (CH) by first reacting the oxidized GE with thionyl chloride to form acyl-chlorinated GE. This product is subsequently dispersed in chitosan and covalently grafted to form GE-chitosan. GE-chitosan is further grafted onto polymetanitroaniline (PMNA) by free radical polymerization conditions to yield GE-CH-PMNA. We have characterized the structure of synthesized GE-CH-PMNA composites by X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FTIR), thermogravimetric analysis (TGA), scanning electron microscopy, and conductivity measurements. XRD data suggest the strongly crystalline character of the prepared specimen. Our measurement shows that the dielectric constants of these nanocomposites are remarkably enhanced due to interfacial polarization effect. This study demonstrates that functionalized graphene sheets are ideal nanofillers for the development of new polymer composites wit...
Research Updates on Graphene Oxide-Based Polymeric Nanocomposites
Graphene oxide (GO) is a carbon-based material, which is one atom thick sheet of graphite. The nanofillers have exceptional stiffness and strength owing to the presence of two-dimensional graphene backbone. Especially owing to this reason, nanocomposites have been developed using GO for several applications. This review article explores the synthesis of GO from flake graphite. Main emphasis has been afforded on the preparation and characterization of GO nanocomposites, utilizing various industrial polymers for wide application in aerospace, biomedical, military, supercapacitors, electrical, sensor, and so on. Morphological characterization exploring the interaction and extent of dispersion of GO nanosheets in the polymer matrices is extensively accounted. From the reports, it is clear that exfoliation and strong interaction of GO tremendously improved the physical, mechanical, thermal, electrochemical, biocompatibility, and tribological properties of the added polymer.
Journal of Thermoplastic Composite Materials, 2018
Reduced graphene oxide (RGEO) and N-[4-(chlorocarbonyl)phenyl]maleimide-functionalized reduced graphene oxide (MFRGEO) were used as nanofillers for poly-methyl methacrylate (PMMA) matrix nanocomposites to enhance thermal stability. Methyl methacrylate containing nanofiller of four different weight percent (0.2, 0.4, 0.6, and 0.8) was polymerized using ultrasonic radiation-assisted bulk polymerization. The Fourier-transform infrared spectra showed the absence of chemical interaction between the filler and the matrix phase. Morphology of nanocomposites studied using scanning electron microscope confirmed the assistance aided by ultrasonication in the uniform dispersion of nanofiller in the PMMA matrix. Thermogravimetric (TG) study revealed the presence of MFRGEO enhanced the thermal stability of PMMA by shifting the entire degradation to higher temperature. The thermal stability of PMMA nanocomposite was improved by as much as 40 C at just 0.8 wt% loading of MFRGEO. Differential TG study also supported the role of maleimide functionalization on RGEO in the enhancement of thermal stability of PMMA by means of retarding the degradation rate of unsaturated chain ends in the PMMA matrix. Unlike MFRGEO, RGEO failed to enhance the thermal stability of PMMA.
The effect of modified graphene (MG) and microwave irradiation on the interaction between graphene (G) and poly(styrene-comethyl meth acrylate) [P(S-co-MMA)] polymer matrix has been studied in this article. Modification of graphene was performed using nitric acid. P(S-co-MMA) polymer was blended via melt blending with pristine and MG. The resultant nanocomposites were irradiated under microwave at three different time intervals (5, 10, and 20 min). Compared to pristine graphene, MG showed improved interaction with P(S-co-MMA) polymer (P) after melt mixing and microwave irradiation. The mechanism of improved dispersion and interaction of modified graphene with P(S-co-MMA) polymer matrix during melt mixing and microwave irradiation is due to the presence of oxygen functionalities on the surface of MG as confirmed from Fourier transform infrared spectroscopy. The formation of defects on modified graphene and free radicals on P(S-co-MMA) polymer chains after irradiation as explained by Raman spectroscopy and X-Ray diffraction studies. The nanocomposites with 0.1 wt% G and MG have shown a 26% and 38% increase in storage modulus. After irradiation (10 min), the storage modulus further improved to 11.9% and 27.6% of nanocomposites. The glass transition temperature of nanocomposites also improved considerably after melt mixing and microwave irradiation (but only for polymer MG nanocomposite). However, at higher irradiation time (20 min), degradation of polymer nanocomposites occurred. State of creation of crosslink network after 10 min of irradiation and degradation after 20 min of irradiation of nanocomposites was confirmed from SEM studies.
Polish Journal of Chemical Technology, 2014
This work is the continuation and refi nement of already published communications based on PET/EG nanocomposites prepared by in situ polymerization 1, 2 . In this study, nanocomposites based on poly(ethylene terephthalate) with expanded graphite were compared to those with functionalized graphite sheets (GO). The results suggest that the degree of dispersion of nanoparticles in the PET matrix has important effect on the structure and physical properties of the nanocomposites. The existence of graphene sheets nanoparticles enhances the crystallization rate of PET. It has been confi rmed that in situ polymerization is the effective method for preparation nanocomposites which can avoid the agglomeration of nanoparticles in polymer matrices and improve the interfacial interaction between nanofi ller and polymer matrix. The obtained results have shown also that due to the presence of functional groups on GO surface the interactions with PET matrix can be stronger than in the case of exfoliated graphene (EG) and matrix.
Poly(urethane-co-vinyl imidazole)/graphene nanocomposites
Polymer Composites, 2012
Poly(urethane-co-vinyl imidazole) (PUVI)/graphene nanocomposites were facilely prepared by a kind of noncovalent way. Herein, the 1-vinylimidazole acted as dispersion agent as well as monomer, graphene was uniformly dispersed in the copolymer matrix without obviously agglomeration. A significant enhancement of mechanical and thermal properties of the PUVI/graphene nanocomposites were obtained at low graphene loading; specifically, a 147% improvement of tensile strength, a nearly 10 times increase of elastic modulus and a 128C enhancement of thermal decomposition temperature were achieved at a graphene loading of 1.5 wt%. Moreover, the volume resistivity of the PUVI/graphene nanocomposites decreased by an order of magnitude after adding 0.5 wt% graphene, demonstrating an obvious change in the electrical property of the nanocomposites prepared.
2013
In the present study, graphene-based nanocomposites containing different amounts of nanofiller dispersed into Bis-GMA/tetraethyleneglycol diacrylate (Bis-GMA/TEGDA) polymer matrix have been prepared. In particular, the graphene dispersions, produced at high concentration (up to 6 mg/ml) by simple sonication of graphite in TEGDA monomer, have been used for the direct preparation of nanocomposite copolymers with Bis-GMA. The morphology of the obtained nanocomposites has been investigated as well as their thermal and mechanical properties. SEM analyses have clearly shown that graphene deeply interacts with the polymer matrix, thus resulting in a reinforcing effect on the material as proved by compression and hardness tests; at variance, graphene does not seem to affect the glass transition temperature of the obtained polymer networks.
Recent Advances in Fabrication and Characterization of Graphene-Polymer Nanocomposites
Graphene has attracted considerable interest over recent years due to its intrinsic mechanical, thermal and electrical properties. Incorporation of small quantity of graphene fillers into polymer can create novel nanocomposites with improved structural and functional properties. This review introduced the recent progress in fabrication, properties and potential applications of graphene-polymer composites. Recent research clearly confirmed that graphene-polymer nanocomposites are promising materials with applications ranging from transportation, biomedical systems, sensors, electrodes for solar cells and electromagnetic interference. In addition to graphene-polymer nanocomposites, this article also introduced the synergistic effects of hybrid graphene-carbon nanotubes (CNTs) on the properties of composites. Finally, some technical problems associated with the development of these nanocomposites are discussed. D. GALPAYA ET AL. 31 the 90% transmittance group is 8.5, 5.0, 2.9 and 8.1 nm from left to right. The corresponding thickness averages are 55.3, 30.9, 66.9 nm for the films in the 30% transmittance group. Reprinted with the permission from reference [29].