Synthetic possibility of polystyrene functionalization based on hydroxyl groups of graphene oxide as nucleophiles

2015 ◽  
Vol 39 (7) ◽  
pp. 5096-5099 ◽  
Author(s):  
Rongbing Yu ◽  
Shupeng Zhang ◽  
Yuting Luo ◽  
Ruofei Bai ◽  
Jiangfang Zhou ◽  
...  
Keyword(s):  
Graphene Oxide ◽  
Nucleophilic Substitution ◽  
Hydroxyl Groups ◽  
Chemical Functionalization ◽  
Wet Chemical ◽  
Heterogeneous Phase

The successful wet chemical functionalization of graphene oxide with polystyrene offered the possibility of nucleophilic substitution in heterogeneous phase reactions.

Enhancement of Hydrophobility and Thermal Property of Graphene Oxide by Paratoluidine Chemical Functionalization

2014 ◽  
Vol 809-810 ◽  
pp. 243-247
Author(s):  
Zhi Jia Luo ◽  
Hong Zhang Geng ◽  
Song Ting Zhang ◽  
Bao Tan Du ◽  
Xing Zhang ◽  
...  
Keyword(s):  
Drug Delivery ◽  
Graphene Oxide ◽  
Thermal Property ◽  
Functional Groups ◽  
Drug Delivery Systems ◽  
Graphite Powder ◽  
Hydroxyl Groups ◽  
Chemical Functionalization ◽  
Hummers Method ◽  
Modified Hummers Method

Graphene oxide (GO) is typically synthesized by graphite powder under strong oxidizing reaction, possessing with the same set of functional groups: epoxy and hydroxyl in basal plane and carboxyl and hydroxyl groups existence on the flake edges which endow GO with amphipathy. GO and its functionalized derivatives have been successfully tested in many domains, such as polymer composites, biosensors, drug delivery systems, etc. In this paper, GO was prepared by a modified Hummers method employing improved process (preparation and separation), aiming at industrialization with the lowest cost. Moreover, some novel functional groups with different properties were controlled chemically grafted onto GO to modify the wettability and reaction activity with other materials. The hydrophobicity and the thermal property of graphene oxide were enhanced by chemical functionalization.

Controlled Functionalization of Graphene by Oxo-addends

2017 ◽  
Vol 2 (3) ◽  
Author(s):  
Siegfried Eigler ◽  
Andreas Hirsch
Keyword(s):  
Graphene Oxide ◽  
Carbon Layer ◽  
Lattice Defects ◽  
Hydroxyl Groups ◽  
Functionalized Graphene ◽  
Chemical Functionalization ◽  
Layer Graphene ◽  
Number Of Layers ◽  
Carbon Framework ◽  
Derivatives Of

AbstractThe single carbon layer graphene and especially its oxidized derivatives, such as graphene oxide (GO), are in the focus of research that started already 150 years ago [1–6]. GO is a collective term for various single layers of graphene (with lattice defects) functionalized by oxo-addends. The type of oxo-groups is not defined, but epoxy and hydroxyl groups dominate the structure in addition to in-plane lattice defects on the percent scale. Those defects are rarely considered in chemical functionalization approaches and it is impossible to distinguish between functionalization of surface oxo-groups and in-plane oxo-groups.This chapter focuses on functionalized derivatives of graphene with an almost intact carbon framework, termed “oxo-functionalized graphene” (oxo-G1, index indicates the number of layers). Avoiding in-plane defects further allows the development of a controlled chemistry of graphene with oxo-addends. However, general approaches of conventional GO chemistry are summarized in a separate section.

scholarly journals Mechanical Properties of Graphene Oxide Coupled by Multi-Physical Field: Grain Boundaries and Functional Groups

Crystals ◽  
2021 ◽  
Vol 11 (1) ◽  
pp. 62
Author(s):  
Xu Xu ◽  
Zeping Zhang ◽  
Wenjuan Yao
Keyword(s):  
Mechanical Properties ◽  
Graphene Oxide ◽  
Grain Boundaries ◽  
Functional Groups ◽  
Oxygen Content ◽  
Tensile Fracture ◽  
Hydroxyl Groups ◽  
Molecular Configuration ◽  
Spatial Design ◽  
Out Of Plane

Graphene and graphene oxide (GO) usually have grain boundaries (GBs) in the process of synthesis and preparation. Here, we “attach” GBs into GO, a new molecular configuration i.e., polycrystalline graphene oxide (PGO) is proposed. This paper aims to provide an insight into the stability and mechanical properties of PGO by using the molecular dynamics method. For this purpose, the “bottom-up” multi-structure-spatial design performance of PGO and the physical mechanism associated with the spatial structure in mixed dimensions (combination of sp2 and sp3) were studied. Also, the effect of defect coupling (GBs and functional groups) on the mechanical properties was revealed. Our results demonstrate that the existence of the GBs reduces the mechanical properties of PGO and show an “induction” role during the tensile fracture process. The presence of functional groups converts in-plane sp2 carbon atoms into out-of-plane sp3 hybrid carbons, causing uneven stress distribution. Moreover, the mechanical characteristics of PGO are very sensitive to the oxygen content of functional groups, which decrease with the increase of oxygen content. The weakening degree of epoxy groups is slightly greater than that of hydroxyl groups. Finally, we find that the mechanical properties of PGO will fall to the lowest values due to the defect coupling amplification mechanism when the functional groups are distributed at GBs.

scholarly journals Graphene oxide chemically decorated with hybrid Ag-Ru/chitosan nanoparticles: fabrication and properties

2015 ◽  
Author(s):  
Murugan Veerapandian ◽  
Suresh Neethirajan
Keyword(s):  
Graphene Oxide ◽  
Chitosan Nanoparticles ◽  
Hybrid Nanoparticles ◽  
Spectroscopic Techniques ◽  
Wet Chemical ◽  
Amine Groups ◽  
Oxygenated Functional Groups ◽  
Coordination Reaction

Hybridization of distinct materials into a single nanoplatform is relevant to advance material’s properties for functional application such as biosensor platform. We report the synthesis and characterization of nanosheets of graphene oxide decorated with hybrid nanoparticles of silver-ruthenium bipyridine complex (Ag@[Ru(bpy)3]2+) core and chitosan shell. Hybrid nanoparticles were first obtained through a sequential wet-chemical approach using in situ reduction, electrostatic and coordination reaction. Oxygenated functional groups of graphene oxide and abundant amine groups of chitosan layer on the surface of hybrid nanoparticles allowed the functionalization reaction. Changes in intrinsic optical, chemical and structural properties of graphene oxide due to hybrid nanoparticles were studied in depth using spectroscopic techniques and an electron microscope. Electrodes modified with nanosheets of graphene oxide-hybrid nanoparticles retain the biocompatibility and displayed an amplified redox property suitable for a broad range of sensing studies.

scholarly journals Effect of Graphene oxide or Functionalized Graphene Oxide on the Copolymerization Kinetics of Styrene/n-butyl Methacrylate

Polymers ◽  
2019 ◽  
Vol 11 (6) ◽  
pp. 999 ◽  
Author(s):  
Ioannis Tsagkalias ◽  
Afrodite Vlachou ◽  
George Verros ◽  
Dimitris Achilias
Keyword(s):  
Graphene Oxide ◽  
Radical Copolymerization ◽  
Butyl Methacrylate ◽  
Side Reactions ◽  
Hydroxyl Groups ◽  
Functionalized Graphene ◽  
Functionalized Graphene Oxide ◽  
Molecular Weights ◽  
Diffusion Controlled ◽  
Kinetic Rate Constants

Nanocomposite materials based on copolymers of styrene and n-butyl methacrylate with either graphene oxide (GO) or functionalized graphene oxide (F-GO) were synthesized using the in-situ bulk radical copolymerization technique. Reaction kinetics was studied both experimentally and theoretically using a detailed kinetic model also taking into account the effect of diffusion-controlled phenomena on the reaction kinetic rate constants. It was found that the presence of GO results in lower polymerization rates accompanied by the synthesis of copolymers having higher average molecular weights. In contrast, the presence of F-GO did not seem to significantly alter the conversion vs time curves, whereas it results in slightly lower average molecular weights. The first observation was attributed to side reactions of the initiator primary radicals with the hydroxyl groups on the surface of GO, resulting in lower initiator efficiency, whereas the second to grafted structures formed from copolymer macromolecules on the F-GO surface. The copolymerization model predictions including MWD data were found to be in satisfactory agreement with the experimental data. At least four adjustable parameters were employed and their best-fit values were provided.

scholarly journals Chemical and structural properties of reduced graphene oxide—dependence on the reducing agent

2020 ◽  
Vol 56 (5) ◽  
pp. 3738-3754
Author(s):  
B. Lesiak ◽  
G. Trykowski ◽  
J. Tóth ◽  
S. Biniak ◽  
L. Kövér ◽  
...  
Keyword(s):  
Graphene Oxide ◽  
Reduced Graphene Oxide ◽  
Sodium Borohydride ◽  
Reduction Rate ◽  
Graphite Powder ◽  
Hydroxyl Group ◽  
Hydroxyl Groups ◽  
Vacancy Defects ◽  
Group Reduction ◽  
Reduced Graphene

AbstractGraphene oxide (GO) prepared from graphite powder using a modified Hummers method and reduced graphene oxide (rGO) obtained from GO using different reductants, i.e., sodium borohydride, hydrazine, formaldehyde, sodium hydroxide and L-ascorbic acid, were investigated using transmission electron microscopy, X-ray diffraction, Raman, infrared and electron spectroscopic methods. The GO and rGOs’ stacking nanostructure (flake) size (height x diameter), interlayer distance, average number of layers, distance between defects, elementary composition, content of oxygen groups, C sp3 and vacancy defects were determined. Different reductants applied to GO led to modification of carbon to oxygen ratio, carbon lattice (vacancy) and C sp3 defects with various in-depth distribution of C sp3 due to oxygen group reduction proceeding as competing processes at different rates between interstitial layers and in planes. The reduction using sodium borohydride and hydrazine in contrary to other reductants results in a larger content of vacancy defects than in GO. The thinnest flakes rGO obtained using sodium borohydride reductant exhibits the largest content of vacancy, C sp3 defects and hydroxyl group accompanied by the smallest content of epoxy, carboxyl and carbonyl groups due to a mechanism of carbonyl and carboxyl group reduction to hydroxyl groups. This rGO similar diameter to GO seems to result from a predominant reduction rate between the interstitial layers. The thicker flakes of a smaller diameter than in GO are obtained in rGOs prepared using remaining reductants and result from a higher rate of reduction of in plane defects.

scholarly journals Optical Nonlinear Refractive Index of Laser-Ablated Gold Nanoparticles Graphene Oxide Composite

2014 ◽  
Vol 2014 ◽  
pp. 1-8 ◽  
Author(s):  
Amir Reza Sadrolhosseini ◽  
A. S. M. Noor ◽  
Nastaran Faraji ◽  
Alireza Kharazmi ◽  
Mohd. Adzir Mahdi
Keyword(s):  
Particle Size ◽  
Gold Nanoparticles ◽  
Refractive Index ◽  
Graphene Oxide ◽  
Gold Nanoparticle ◽  
Spherical Shape ◽  
Refractive Indices ◽  
Hydroxyl Groups ◽  
Uv Visible ◽  
Laser Ablation Technique

Gold nanoparticles were prepared in graphene oxide using laser ablation technique. The ablation times were varied from 10 to 40 minutes, and the particle size was decreased from 16.55 nm to 5.18 nm in spherical shape. The nanoparticles were capped with carboxyl and the hydroxyl groups were obtained from Fourier transform infrared spectroscopy. Furthermore, the UV-visible peak shifted with decreasing of nanoparticles size, appearing from 528 nm to 510 nm. The Z-scan technique was used to measure the nonlinear refractive indices of graphene oxide with different concentrations and a gold nanoparticle graphene oxide nanocomposite. Consequently, the optical nonlinear refractive indices of graphene oxide and gold nanoparticle graphene oxide nanocomposite were shifted from1.63×10-9 cm2/W to4.1×10-9 cm2/W and from1.85×10-9 cm2/W to5.8×10-9 cm2/W, respectively.

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