Influence of Surface modified Graphene Oxide on Mechanical and Thermal Properties of Epoxy Resin

The principal aim of this work is to investigate the mechanical and thermal properties of graphene oxide reinforced epoxy composites. Surface modification was carried out by 3-aminopropyltriethoxysilane (APTS) with aqueous solution method. Surface modified graphene oxide was mixed in epoxy matrix by sonication process and composites were prepared by compression moulding technique. Three different formats: graphene (G), graphene oxide (GO) and APTS graphene oxide (APTS-GO) were incorporated respectively in an epoxy matrix to form composites. The tensile and impact tests show that the surface modified graphene oxide reinforced epoxy composites gives better results than unmodified graphene oxide reinforced epoxy composites. Scanning electron microscope images revealed that the dispersion of the surface modified graphene oxide on epoxy matrix was better at high frequency sonication than unmodified graphene oxide on epoxy system. The thermal properties of composites were analysed by Differential Scanning Calorimetry (DSC). keywords: Graphene, Graphene Oxide, APTS-GO, SEM, DSC.


INTROdUCTION
Epoxy resin is genetically brittle and this problem can be mitigated by the incorporation of nanoadditives.Although may successful attempts have been made for the development of novel nanocomposites for epoxy resins, however challenges still exist in selection of material and fulfil the potential to achieve a level of performance.So many researches have been conducted to brittle epoxy using additive like block copolymer, rubbers, silicates, liquid crystals, clays, CNT, carbon fiber etc [1][2][3][4] .So, these entire additives generally reinforced the toughness of the composites at the cost of its thermal decomposition temperature or glass transition temperature (tg).Unalike other additives, functionalized graphene oxide reinforced the fracture toughness of composites without altering its thermal decomposition temperature or glass transition temperature (tg) [5][6] .
A single layer graphene is sp 2-hybridized carbon and two dimensional honeycomb lattice structures.It has attracted amazing growing attention in the past several years, As a result of its outstanding behaviour in optic, mechanical, thermal, electrical and other properties 7 .According, polymer composites have various uses like adhesive, coating, electronic, automobile, aircraft, aerospace etc. Pure form of graphene and graphene oxide is not adaptable with either polymers or organic solvents and does not form comparable composites [8][9][10] .To improve the distribution of graphene oxide in a polymer, reduction, oxidation and various functionalization of the carbonaceous surface is required.Graphene oxide has been mainly synthesised by the Hummer's methods and modified hummer's methods [11][12][13] .The surface functional groups of Graphene oxide are carboxylic acids, alcohols, epoxides and other ketone groups.The percentage of these functional groups can vary significantly, depending on the initial material.
Polymer/graphene oxide nanocomposites obtain superior thermal, mechanical, morphological and electrical properties as compared to neat polymers, observed by Jiacheng Wei et al., 14 .Le et al., 15 in composition 0.5 wt% silane graphene oxide/epoxy composites by bath sonication and mechanical mixing enhance 16% and 20% in tensile strength and elastic modulus as compared to neat epoxy.Equivalently, Rafiee et al., 16 recorded a significant increment in Young's modulus at 0.1 wt% of graphene/epoxy composites fabricated by sonication.Qi et al., 17 reported thermotropic liquid crystalline epoxy functionalize graphene oxide and the assemble composites enhance 42.5% and 100% at 1 wt% in tensile strength and impact strength.
In this work, researcher investigates the surface functionalize graphene oxide with APTS (3-aminopropyltriethoxysilane) using aqueous solution method.The epoxy composites with Graphene, Graphene oxide (GO) and APTS graphene oxides (APTS-GO) were prepared.Researcher observed improved dispersion of APTS-GO in epoxy resin when compared to that of GO and Graphene prepared with similar process with epoxy resin.Moreover, the thermal and mechanical properties were measured and compared to further understand the role of APTS onto GO surface of composites.

Preparation of Graphene Oxide
For synthesis of graphene oxide modified Hummer's method was used 18 .Graphene (3 g), sodium nitrate (1.5 g) and 70 ml sulphuric acid were added in beaker on an ice bath.Gradually KMnO 4 was added to maintaining the temperature under 20 o C for 1 hour.The mixture was kept on an ice bath for 2 h, followed by keeping at room temperature for next 2 hours.Drop by drop deionized water was added when the mixture turned into a highly-viscous liquid, maintaining mixture temperature around 50 o C. 300 ml water and 10 ml hydrogen peroxide (30 wt% aqueous solutions) was added to for terminate the reaction.The mixture was centrifuged and washed by deionized water till pH become ~7.The product obtained was dried in a vacuum oven.

Preparation of Functionalized Graphene Oxide
Around 4g NaOH was added into GO solution (600 mg GO in 500 ml water) under stirring.After complete dissolve of NaOH, the mixture was refluxed at 80 o C for 3 h followed by centrifugation.The black particle obtained was re-acidified with 600 ml HCl (0.1M) and again refluxed for one hour again.The suspension was washed using distilled water till it become neutral and product was filtered and dried in a vacuum oven.About 2g APTS was first diffuse in ethanol and water (75:25 by volume).Around 200 mg above product was mix in to the mixture with sonication for 1 h and refluxed for 4 h with heating.For removable the residual coupling agents mixture was centrifuged and washed by same mixture of ethanol/water.Obtained functionalised GO particles were vacuum drying overnight.

Preparation of Nanocomposites
S o l u t i o n s o f g r a p h e n e, g r a p h e n e oxide and APTS-GO in acetone were sonicated for 1 hour.Liquid epoxy was added in above f i l l e r / a c e t o n e s o l u t i o n a n d s o n i c a t e d fo r one hour.When homogenous mixture was obtained, the mixture was stirred at 70 o C for 4 hours.The mixtue solution was kept in a vacuum oven at 80 o C for till assure of complete removal of acetone.Amine hardener (TETA) was mixed thoroughly for approximately 5 min., by mechanical stirring.The mixture was kept in vacuum oven to degas for 1 h and poured into silicon moulds for various specimen and cured at room temperature for 24 h and post curing for 8 h at 100 o C.

Characterization
T h e m e c h a n i c a l p r o p e r t i e s o f nanocomposites were measured on a universal testing machine (Zwick 010) with a 5kN load cell and tests were performed at 27 o C and 50% humidity and dumbbell-shaped samples with crosshead speed of 2mm/minute.The at least five specimen were tested for each composite.Differential scanning calorimetric (Mettler Toledo, DSC instrument) analysis was carried out with a heating rate of 10 O C/min. in nitrogen (40 mL/minute).Field emission scanning electron microscopy (FESEM) (SIGMA, CARL ZEISS, Germany) was used for surface morphology and fractographic study.Earlier to imaging the composite were coated with gold-palladium sputtering.Fourier transform infrared (FTIR) spectra were reported using a powder in KBr pellets using vertex 70V, Bruker Optik in the transmission mode.Raman spectra were recorded using STR 500 CONFOCAL MICRO RAMAN SPECTRO with 50x objective lens at room temperature, a 633 nm He-Ne laser beam.

Characterization of Graphene, Graphene Oxide and APTS-GO
Figure 1 present FTIR spectra of graphene, graphene oxide and APTS-GO, show that there is a clear change in Graphene, GO and APTS-GO.Several absorption bands can be found for Graphene Oxide: an intense and broad band at 3450-3600 cm -1 attributed to O-H stretching vibration, at 1723 cm -1 band assigned to carboxyl groups or C=O stretching of carbonyl, a band detect at 1620 cm -1 assigned to un-oxidized graphitic domain and at 1401cm -1 and 1098 cm -1 band equivalent to in plane -COH bending and epoxy C-O-C bond, respectively.These results confirm the successful preparation of Graphene Oxide (GO).Besides, an important peak appear in GO indicating the affluence hydroxyl, carboxyl and epoxy group which can act as active sites to implant functional molecules into the board of graphene oxide.
After salinization of APTS, new spectral features view in APTS-GO spectrum (Fig. 1).The band at 2920 and 2850 cm -1 are assigned to stretching vibration of -CH 2 groups, Stretching vibration of the -CO-group is attributed to an absorption band at 1720 cm -1 .A strong band at 1075 cm -1 and 1395 are due to the stretching vibration of SiO and SiCH 2 bands, respectively.The band corresponding to the amine groups of the APTS units on the graphene sheets at 2830 cm -1 , indicates that amine group has been strongly imported into the surface of the graphene oxide.Usually, the characteristic peaks of hydrophilic group (eg -COOH and -OH) can be shown with high intensity, which show that the whole process of modification did not lead to the modification of the graphene oxide.
Raman spectroscopy is helpful to study the defect and disorder in structure of crystal and characterization study of graphene and derivatives of graphene.Intensity ratio between the disorder induced D band (Id) and Raman allowed G band (IG) is used to determine disorder.Fig. 2 presents Raman spectra of graphene, graphene oxide and APTS-GO.The G band is at 1597 cm -1 , 1607 cm -1 and 1595 cm -1 and D band is at 1365 cm -1 , 1364 cm -1 and 1355 cm -1 for Graphene, Graphene Oxide and APTS-GO respectively.In graphene oxide D band is broadened arises to decreases in size of the sp 2 domains by the formation of vacancies, distortion and defects during oxidation.For all sp 2 carbon from, G band is common and it due to C-C band stretch and make by first order Raman scattering.In graphene oxide spectrum, the G band is switch to higher wavenumber as a result oxygenation of graphene that leads to formation of sp 3 carbon atoms.The decreases of intensity ratio from 1.03 (Graphene Oxide) to 0.7 (Graphene) prove the implant of functional groups consisting oxygen to the graphene.In the APTS-GO, number of sp 2 carbon atoms increases so G band shifted to lower wavenumber.During reduction D band intensity is lowered, but not enough as comparison to graphene and graphene oxide.The intensity ratio becomes 0.93 for APTS-GO which reveals that removal of almost all the functional groups consisting oxygen.The ratio of Id/IG in APTS-GO is higher than that of graphene oxide and graphene because of the newly formed sp 2 domains during reduction process.resin and its composites also exhibit brittle behaviour.Stress-strain curve of the epoxy composites obtained in tensile testing are shown in Fig. 3(A).Fig. 3(B) present tensile strength was varied with the filler contents.All composites show linear stress-stain character up to failure, without plastic deformation and all specimen exhibit similar curve shape.The results also show an increment in tensile strength and young's modulus of composites as compared to neat epoxy.In other word, the dispersion of amine functionalized graphene oxide in epoxy resin show high reinforcement in the mechanical properties as compared to neat epoxy.Figure 3 (B,D) present the variation in tensile strength and impact strength of the composites.Clearly, the tensile strength and impact strength of the composites are improved effectively on addition of fillers.As shown in figure, for neat epoxy tensile strength and impact strength are 54MPa and 26.15KJ/m -2 respectively.The composite with APTS-GO show the highest values of tensile strength (76 MPa) and impact strength (54.43 KJ/m -2 ), around 41% and 97% larger than that of neat epoxy resin.This is attributed to the large surface area and multiple interactions between the matrix and functional groups of the fillers in the composites.
However, a little increment in toughness and ductility was shown upon the addition of Graphene, Graphene Oxide and APTS-GO probably due to the energy dissipation at the interface between the matrix and the filler.Such increment in ductility is comparably significant for Graphene Oxide/epoxy composites.Fig. 3(C) shows the Young's Modulus (E).The addition of nanoparticles improves the modulus without leading to reduction in strain to failure.The nanocomposite with APTS-GO shows best mechanical properties with 37.5% increment of Young's Modulus.In general, the characteristic improvement in the mechanical properties is ascribed to a powerful interaction between surface modified graphene oxide and matrix.So, the effective load transfer between nanoparticle and the matrix can take place.Additionally, the nanoparticles may play as connecting bridges to avoid the matrix from fracturing upon mechanical deformation hence improving the mechanical properties of epoxy.

Mechanical Properties of Composites
T h e m e c h a n i c a l p r o p e r t i e s o f nanocomposites are summarized in Figure 3 and Table 1.The toughness of composites was calculated by the area of the stress-strain curve.The epoxy For analysis of composites, it is essential to notice that there are any other overlapping transitions.Kinetic events are functions of both temperature and time like decomposition, cure, evaporation etc.The transition will be shifted to a higher temperature at higher heating rates as a result of the epoxy achieves minimum time for transitioning at a particular temperature.Hence, higher heating rate increases the resolution because composites achieve sufficient time to transition at a particular temperature.There is only one exothermic peak for all four specimens as show in Fig. 4. So, epoxy composites with graphene, graphene oxide and APTS-GO as compare to neat epoxy lower the exothermic peak height which signifies enhanced degree of interaction as well as physical hindrance.The effect of graphene, graphene oxide and APTS-GO on epoxy can be confirmed by peak temperature (Tp) and onset temperature (Ti) and the total heat of reaction (ΔH), listed in Table 2. Table show that heat of reaction is decreasing because well distributed fillers can act as physical hindrance to the movability of polymeric molecule and lower movability of polymeric chain may conclusion in  Fracture Mechanisms via Fractography Figure 5 presents the FESEM images of fracture surface of composites.The fracture surfaces of all composites show the river mark like design.
These river marks like designs were expectably to be developed at the time of the crack propagation.
So, these designs suggest the fracture to be a mix manner (shear and tensile) of failure.As shown in Fig. 5, neat epoxy comparably less in number of river like design with flat fracture surface.This indicates restricted plasticity on the crack tips and very quick crack propagation.In comparison to neat epoxy, sample with nanofiller show higher number of river like design with fracture rougher surface.Furthermore, the composites with fractured surfaces show ductile and coarser morphology as compared to neat epoxy.This manner can be interrupted by deflection phenomena in which nanofiller show in a way of propagating crack, the crack is expectedly to deflect and taken lengthy way in order to propagate again, which is surely visible from higher magnify fractographs.Hence, as a result of crack deflection, higher energy is possible to absorb than when in the way of crack show no obstacle.

CONCULSION
In this paper, we have demonstrated the advantage of functional group attached to graphene oxide and upon their addition to an epoxy resin.In comparison to neat epoxy, the young's modulus, tensile strength and impact strength of composites were increased and the best increments were observed for APTS-GO, which can be attributed to the strong covalent bonding between the APTS-GO and epoxy resin leading to good load transfer.Fractography recommended that the primary toughing mechanism in composites was primarily due to the mutual effects of expanded plastic deformation near the crack deflection and crack tip.Thus, the amine functionality of GO is able to manipulate the specific characterization of GO, indicating the potential to design modification of GO to make it more suitable for applications in a variety of polymer-based nanocomposites, not only for mechanical performance, but also for controlling barrier and other function properties.