Investigation of the Impact of Graphene Nanostructure on the Mechanical Properties of Tires Compounds

Document Type : Original Research Article

Authors

1 MSc, Department of Physics, Faculty of Sciences, University of Mohaghegh Ardabili, Ardabil, Ardabil, Iran

2 Associate Professor, Department of Physics, Faculty of Sciences, University of Mohaghegh Ardabili, Ardabil, Ardabil, Iran

3 Associate Professor, Department of Physics, Faculty of Sciences, Imam Khomeini International University, Qazvin, Qazvin, Iran

4 Associate Professor, Department of Engineering Sciences, Faculty of Advanced Technologies, University of Mohaghegh Ardabili, Namin, Ardabil, Iran

Abstract

Numerous researchers have shown interest in the new technique of adding various nanoparticles to elastic materials in an attempt to improve their properties. Physical qualities such as wear resistance, strength, thermal properties, tear limit, and elastic fracture were improved as a result of the atomic scale bonds between the nanoparticles and elastic compounds. These characteristics will in turn lead to high-quality and market-friendly products that can compete in international markets. According to the literature, various nanoscale materials including graphene, calcium carbonate (CaCO3) nanoparticles, aluminum nanoparticles, diamond nanoparticles, nanoclays, and zinc oxide nanoparticles have been widely used in the rubber industry. Development of significant CaCO3 nanoparticle structures has continued to date. Carbon nanotubes are another type of nanoscale that can be employed in the rubber industry. In this paper, the effect of graphene on the mechanical properties of rubber compounds was studied due to the significance of incorporation of graphene into the composites, especially into the rubber compounds. The obtained results demonstrated that mechanical properties including tensile strength, wear resistance, and elongation percentage could be easily enhanced by adding graphene to rubber materials. The authors hope that these enhanced compounds will be applicable to the industrial production.

Highlights

  • We study the new trend of adding various nanoparticles to elastic materials.
  • The effect of graphene on the mechanical properties of rubber compounds has been studied.
  • The obtained results have demonstrated that mechanical properties including tensile strength, wear resistance, and elongation percentage can be easily enhanced by adding graphene to rubber materials.

Keywords

Main Subjects


Advanced Ceramics Progress: Vol. 8, No. 4, (Autumn 2022) 42-47

Materials and Energy Research Center MERC Contents lists available at ACERP Advanced Ceramics Progress Journal Homepage:www.acerp.ir Original Research Article Investigation of the Impact of Graphene Nanostructure on the Mechanical Properties of Tires Compounds Kazem Jeddi a, Farhad Sattari b,, Seyedeh Zahra Mortazavi c, Soghra Mirershadi d a MSc, Department of Physics, Faculty of Sciences, University of Mohaghegh Ardabili, Ardabil, Ardabil, Iran b Associate Professor, Department of Physics, Faculty of Sciences, University of Mohaghegh Ardabili, Ardabil, Ardabil, Iran c Associate Professor, Department of Physics, Faculty of Basic Sciences, Imam Khomeini International University, Qazvin, Qazvin, Iran d Associate Professor, Department of Engineering Sciences, Faculty of Advanced Technologies, University of Mohaghegh Ardabili, Namin, Ardabil, Iran  Corresponding Author Email: f_sattari@uma.ac.ir (F. Sattari) URL: https://www.acerp.ir/article_161861.html ARTICLE INFO ABSTRACT Article History: Received 14 November 2022 Received in revised form 21 November 2022 Accepted 29 November 2022 Numerous researchers have shown interest in the new technique of adding various nanoparticles to elastic materials in an attempt to improve their properties. Physical qualities such as wear resistance, strength, thermal properties, tear limit, and elastic fracture were improved as a result of the atomic scale bonds between the nanoparticles and elastic compounds. These characteristics will in turn lead to high-quality and market-friendly products that can compete in international markets. According to the literature, various nanoscale materials including graphene, calcium carbonate (CaCO3) nanoparticles, aluminum nanoparticles, diamond nanoparticles, nanoclays, and zinc oxide nanoparticles have been widely used in the rubber industry. Development of significant CaCO3 nanoparticle structures has continued to date. Carbon nanotubes are another type of nanoscale that can be employed in the rubber industry. In this paper, the effect of graphene on the mechanical properties of rubber compounds was studied due to the significance of incorporation of graphene into the composites, especially into the rubber compounds. The obtained results demonstrated that mechanical properties including tensile strength, wear resistance, and elongation percentage could be easily enhanced by adding graphene to rubber materials. The authors hope that these enhanced compounds will be applicable to the industrial production. Keywords: Graphene Tensile Strength Rubber Compound Stress and Strain https://doi.org/10.30501/acp.2022.369482.1111 1. INTRODUCTION The tire industry manufactures a wide variety of tires, including various sized riding tires, motorcycle tires, truck tires, tractor tires, and bicycle tires. Tire tread, grooves, ridges, layers, tire collars, etc. are the basic parts of a tire. Each part of the tire (rubber) is manufactured for a particular purpose with unique properties. In recent years, the characteristics of tires have been significantly improved by adding various nanoparticle combinations. Due to the atomic-scale bonds that exist between the nanoparticles and elastic compounds, the presence of nanoparticles not only enhances the physical properties of the rubber compounds but also increases their wear resistance, strength (improves mechanical properties), thermal properties, and tear and fracture limits [1-3]. These factors come together to produce a high-quality marketable product that can compete on international markets. Numerous nanometer materials such as calcium carbonate (CaCO3) nanoparticles, calcium oxide nanoparticles, alumina nanoparticles, diamond nanoparticles, nanoclays, and fullerenes have reportedly found widespread applications in the rubber industry. However, according to the literature, CaCO3 nanoparticles have recently gained in popularity [4]. Due to the atomic-scale bonds that exist between the nanoparticles and elastic compounds, the presence of nanoparticles enhances the physical properties of rubber compounds. Carbon nanotubes and graphene are two more significant nanostructures that can be used in the rubber industry. In the following, some of the characteristics of graphene will be examined. Pure carbon and graphene atoms are arranged in a regular hexagonal structure, much like graphite but with one-atom thickness, to form graphene. Graphene, one of the carbon allotropes, has a single-sheet structure composed of atoms joined together by strong bonds to form a honeycomb-like crystal network. Graphene is the thinnest, yet strongest, known material discovered so far [5-9]. In this structure, the carbon-carbon bond is 1.42 Å long. One square meter plate of graphene weighs just 0.77 g, making it a lightweight substance. A graphite sheet or crystal is formed of several graphene sheets that are bonded together and are arranged on top of one another at the distance of 3.35 Å. Theoretical physicist Philip Wallace first investigated the theory of graphene in 1947. He made attempts to comprehend the complex electrical characteristics of the three-dimensional graphite at a time when graphene had not yet been given a name. The term graphene, first coined in 1962 by Hans-Peter Boehm, is a combination of the words graphite and its suffix. They employed a transmission electron microscope to examine the single-layer carbon plates; however, graphene had not been yet produced until the 21st century when Professor Andre Geim and Konstantin Novoself in cooperation with their research group from the University of Manchester succeeded in separating single layers of graphene using adhesive tape in 2004 and won the Nobel Prize in Physics in 2010. The Massachusetts Institute of Technology selected graphene as one of the top ten technologies owing to its unique features and the extensive studies conducted on it. Additionally, a scientific journal named it the top-notch scientific achievement of 2009. Graphene is currently the thinnest yet most resistant material in the world. Although it is highly transparent due to its thinness, the smallest gas atom, helium, cannot pass through it due to its high density [10-12]. Single-layer, double-layer, and multi-layer graphene have potential applications in different industries. The hardest and thinnest material ever created by humans is called graphene. Its thinness, which is equal to the thickness of a carbon atom, allows light to pass through it despite its dense structure. Additionally, ease of preparation, conductivity (it is even more conductive than copper), and capacity of graphene to transmit heat and electricity make it a new option to be used in optical screens and computer components. This substance is even harder than diamond with considerble resistance to pressure that causes a disintegration 200 to 300 times greater than that of steel. Owing to its highly desirable lightness and flexibility, graphene is described as a super material which is expected to bring about a revolution in the electronics sector in the future [13]. One of the characteristics that distinguishes graphene from other materials and makes it particularly effective as a reinforcing component in composites is its impressive mechanical properties. The stability of the Sp2 bonds that make up the hexagonal network and resist all types of in-plane deformations are other outstanding mechanical characteristics of graphene [14-16]. 2. MATERIALS AND METHODS A variety of techniques have been employed so far to analyze the investigated graphene including Scanning Electron Microscopy (SEM), Diffusion Reflectance Spectroscopy (DRS), and X-Ray Diffraction (XRD), to name a few, and to evaluate the properties of the crystal structure and determine the network parameters. The following procedure was considered to create the principal compound of 980 KN (2 kg) in a laboratory tank with a nominal capacity of 2.5 liters using a combination of rubber, carbon black, chemicals, oil, and other materials (Table 1). A ram used for pressurization and consiste mixing was employed in conjunction with a laboratory mixer with a volume of 5.2 liters that was made by Samak Iran. The ram is pneumatically operated that works at the pressure of 5 bar. The task of pressurizer is to provide uniform mixing in the mixer chamber. The chemicals, oil, and soot are loaded into the hopper after being weighed and then, the feed door located above the hopper is utilized to feed the materials. The rubbers are poured into the funnel in the first step. Chemicals, carbon, and oil are introduced to the funnel once the temperature reaches 100 °C, with the exception of the chemical curing agents. The temperature serves as the decisive factor of the test. Once the compound was thoroughly mixed and the temperature reached 140 °C, KN compound was discharged until the compound age (rest) time was passed. Once the compound reached its age period, the curing chemical agents were added. Since there was not enough graphene in the lab, 100 g of the initial compound was used. A relatively small laboratory mill was utilized because it was unable to produce 100 g of the chemical in a 2.5-liter beaker. Then, KN compound was softened on the mill as the working technique. Then, in accordance with the instructions given in Table 2, graphene was added to the compound in varying amounts (in the first step, 0.5 g of graphene), and the mixture was thoroughly mixed on a mill (two mills). Next, the curing agents were added to the nano compound, and after 24 hours of aging time, 70 g of the nano compound was baked in a special mold in a laboratory baking press for 30 minutes at the temperature of 155 °C. TABLE 1. Quantities of chemicals required to produce master batch compound or KN Trade name of chemical substances Chemical name The amount of substances (g) The amount of substances (wt. %) SBR1500 Butadiene Starene Rubber 377.2 12.041 PBR1220 Poly Butadiene Rubber 506.5 6.592 SBR1712 Oily Rubber Butadiene Styrene 474.7 15.153 CARBONN375 Carbon 718.4 22.932 AROMATIC OIL Aromatic oil 188.5 6.017 ZNO Zinc Oxide 359.2 11.466 IPPD Antioxidant N-Diparaphenylene isopropyl amine 269.4 8.600 STEARIC ACID Stearic acid 359.2 11.466 TMQ Antioxidant Polymerized 2,2,4-Trimethyl – 1,2- Dihydroquinoline 269.4 5.733 TABLE 2. The fraction of chemicals required to produce the final composition of graphene Baking Factors and Graphene Weight of chemical compounds, Graphene Weight of chemical compounds, Graphene Weight of chemical compounds, Graphene Weight of chemical compounds, Graphene Master Batch (MB) 98.665 98.181 97.701 96.756 CBS Accelerator 0.632 0.629 0.626 0.620 Sulfur 0.637 0.634 0.631 0.625 PVI Anti scorch 0.065 0.065 0.064 0.064 Graphene 0 0.491 0.977 1.935 Following the compound baking step, four samples were created using a punch machine in the shape of dumbbell-shaped strips so that the tests could be performed on the strips. The tensile, wear, and hardness tests are considered the necessary mechanical testing. 3. RESULTS AND DISCUSSION The XRD method was employed to characterize the synthesized graphene and examine the crystal structure properties and establish their lattice parameters. Figure 1 displays the X-ray diffraction spectrum of the synthetic graphene. Figure 1. Graphene's X-ray diffraction spectrum According to the data analysis, the peaks that appear at the angles of 26.3, 43.5, and 54.3 degrees, respectively, refer to the plates with the Miller indices (002), (101), and (004). The observed results, which are consistent with the findings supported by reliable scientific journals, demonstrate that a graphene structure with a lattice constant of 3.34 Å has formed [17–18]. Figure 2 depicts the images captured from the surface of the created graphene samples at different magnifications by scanning electron microscopy that helps examine the surface morphology of the graphene thin layer sample and confirm the creation of graphene nanosheets. As observed in the images, the surface of the created graphene is quite wide, and the folds and bends suggest that the graphene is single-layered. The energy gap of the graphene nanosheets was calculated using the diffusion reflection method. As a result, to determine the energy gap, first, diffuse reflection spectroscopy, capable of measuring the powder samples, was used to determine the reflection spectrum in terms of the wavelength of light. In the diffusion reflectance spectroscopy, the spectrophotometer measures the intensity of the light reflected from the sample and compares it with the that of the light reflected from the surface of the reference sample. The spectrum in Figure 3 depicts the transition of electrons from the valence band to the conduction band as a result of incident photon energy, the cause of light intensity at the relevant wavelength to drop. In other Figure 2. Scanning electron microscope images of graphene nanoparticles magnified by 300 nm in (a), 300 nm in (b), 200 nm in (c), and 100 micrometers in (d) words, there is a decrease in the ratio of the transmitted to the reflected light. As shown in the graphene sample, the amount of light reflection decreased with a decrease in the wavelength of the incident photon from 500 nm to 320 nm. Figure 3. The graphene nanostructure's reflection spectrum as a function of the light's incident wavelength Graphene thin layer energy gap was calculated using Mott and Davis's theory, where the (αhυ)2 curve was drawn in terms of photon energy (hυ). To be specific, the reflection the coefficient R(λ) is considered to derive the absorption coefficient α(υ) = (1 - R)2 / 2R, and the energy gap was then simply calculated by drawing a tangent line on the linear portion of the graph produced from (αhυ)2 in terms of energy [19]. Based on Figure 4, the energy gap for this two-dimensional structure was calculated as approximately 0.8 eV by drawing the tangent line on the graph in the linear region. Figure 4. The curve of changes of (αhν)2 in the two-dimensional graphene nanostructure in terms of photon energy (hν) Following that, the impact of graphene on the mechanical characteristics of the compound was examined in terms of its tensile strength, tearing force, and elongation. This examination in turn had a positive impact on the compound, as shown in Figure 5. Particularly, an increase in the length, tearing force, and tensile strength were all greatly improved by graphene, which accounts for 1.935 wt. % of the material. As the graphene weight increased, the tear force roughly increased proportionally. In diagram (a) attributed to the compound without graphene, the sample is subjected to Figure 5. Compound tension diagram with different amounts of graphene in terms of force-tension the maximum force of 114 N; in other words, the force imposed at the point of rupture was 114 N, and the displacement was 215.54 mm. In addition, the values of stress, strain, and length increase were obtained as 11.4 MPa, 7.18 dimensionless, and 718 %, respectively. Diagram (b) shows a compound containing 0.491 % graphene by weight and the relevant applied force, displacement or stretching, stress, strain, and length increase. In this diagram, the values of the applied force, displacement or stretching, stress, strain, and length increase were obtained as 121.4 N, 215.56 mm, 12.14 MPa, 7.18, and 718.53 %, respectively. The applied force in diagram (c), which represents the compound containing 0.977 % by weight of graphene, is 125.1 N, and the values of displacement or stretching, tension, strain, length increase, and modulus are 212.46 mm, 12.51 MPa, 7.08, 708 %, and 1.69 N/mm2, respectively. In diagram (d), the values of the applied force, displacement, stress, strain, elongation, and modulus in the compound containing 1.935 g of graphene were obtained as 172.9 N, 264.06 mm, 17.29 MPa, 8.88, 880.2 %, and 1.96 N/mm2, respectively. The obtained results are presented in Table 3. TABLE 3. The values obtained from the graph of compound tension with different amounts of graphene in terms of weight percentage Graphene in weight (%) 0 0.491 0.977 1.935 Force (N) 114.0 121.4 125.1 172.9 Tensile (mm) 215.5 215.5 212.4 264.1 Tension (MPa) 11.4 12.1 12.5 17.2 Strain 7.2 7.2 7.1 8.8 Increased length (%) 718.04 718.5 708.0 880.2 Modulus (MPa) 1.5 1.6 1.7 1.9 The A SHORE equipment from Bareiss, Germany, was used to conduct the hardness test, the results of which are given in the following. The reference sample, containing no graphene, yielded 62 ShoreA. In addition, 2, 1, and 0.5 g of graphene yilded ShoreA64.5, ShoreA65, and ShoreA64, respectively, in the samples constructed at various levels of graphene presence. The wear test was completed in two minutes using a wear instrument developed by Bareiss in Germany. The results for the rubber compound containing the nanographene substance are reported in Table 4, and the wear test samples are displayed in Figure 6. The wear test result for graphene with the weight percentages of 0.491 and 0.977 is 80 %, while that for the graphene with the weight percentage of 1.935 is 65 %. Finally, for the reference sample, which is our initial compound without graphene, the result is 145 % TABLE 4. The degree of wear in compounds with a graphene weight fraction The amount of Graphene in compound The amount of wear (%) Without nano 145 0.491 80 0.977 80 1.935 65 Figure 6. Examples of baked mixtures for a hardness test 4. CONCLUSION The current research aims to examine the impact of graphene nanostructure on the elastic compounds, and a summary of the obtained results will be given in the following. The tensile strength, tearing force, and elongation were examined to determine the impact of graphene on the mechanical properties of the compound, and the results showed that graphene had a positive impact on the compound, which was also confirmed in the relevant diagram. Particularly, an increase in the length, tearing force, and tensile strength were all greatly intensified by the presence of graphene, especially the one with the wight percentage of 1.935 %. As graphene weight increased, the tear force was proportionally raised. In the reference compound that contained no graphene, the greatest force imposed on the sample, the amount of force applied at the moment of rupture, was 114 N, and displacement was 215.54 mm. In addition, the values of stress, strain, and length increase were obtained as 11.4 MPa, 7.18 without dimension, and 718 %, respectively. The displacement or amount of tension in the compound with the weight percentage of 0.491 was measured as 215.56 mm, applied force as 121.4 N, stress as 12.14 MPa, strain as 7.18, and length increase as 718.53 %. The modulus of the compound with the weight percentage of 0.977 was 1.76 N/mm2. The values of the applied force, displacement or amount of tension, stress, strain, was and length increase were measured as125.1 N, 212.46 mm, 12.51 MPa, 7.08, and 708 %, respectively. In the compound with an applied force of 172.9 N and the displacement or tension of 264.06 mm, the stress velue of was obtained as17.29 MPa, strain as 8.88, length increase as 880.2 %, and modulus as 1.96 N/mm2, respectively. The results from wear and hardness tests showed that the strength of the elastic compound could be greatly enhanced by adding graphene nanostructure. ACKNOWLEDGEMENTS The authors would like to express their gratitude to the management and personnel of the Artaville Tire Ardabil factory for their cooperation and assistance. REFERENCES 1. Wang, W., Wang, S., Ma, X., Gong, J., “Recent advances in catalytic hydrogenation of carbon dioxide”, Chemical Society Reviews, Vol. 40, No. 7, (2011), 3703-3727. https://doi.org/10.1039/C1CS15008A 2. Yan, L., Wang, J., Han, X., Ren, Y., Liu, Q., Li, F., “Enhanced microwave absorption of Fe nanoflakes after coating with SiO2 nanoshell”, Nanotechnology, Vol. 21, No. 9, (2010), 095708. https://doi.org/10.1088/0957-4484/21/9/095708 3. Lehman, K., “Reviews of science for science Librarians: Graphene”, Science & Technology Libraries, Vol. 30, No. 2, (2011), 132-142. https://doi.org/10.1080/0194262X.2011.575628 4. Shao, H. Q., Wei, H., He, J. 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Please cite this article as: Jeddi, K., Sattari F., Mortazavi S. Z., Mirershadi, S., “Investigation of the Impact of Graphene Nanostructure on the Mechanical Properties of Tires Compounds”, Advanced Ceramics Progress, Vol. 8, No. 4, (2022), 42-47. https://doi.org/10.30501/acp.2022.369482.1111 2423-7485/© 2022 The Author(s). Published by MERC. This is an open access article under the CC BY license (https://creativecommons.org/licenses/by/4.0/).

Open Access

This is an open access article under the CC BY license (https://creativecommons.org/licenses/by/4.0/).

  1. Wang, W., Wang, S., Ma, X., Gong, J., “Recent advances in catalytic hydrogenation of carbon dioxide”, Chemical Society Reviews, 40, No. 7, (2011), 3703-3727. https://doi.org/10.1039/C1CS15008A
  2. Yan, L., Wang, J., Han, X., Ren, Y., Liu, Q., Li, F., “Enhanced microwave absorption of Fe nanoflakes after coating with SiO2 nanoshell”, Nanotechnology, 21, No. 9, (2010), 095708. https://doi.org/10.1088/0957-4484/21/9/095708
  3. Lehman, K., “Reviews of science for science Librarians: Graphene”, Science & Technology Libraries, 30, No. 2, (2011), 132-142. https://doi.org/10.1080/0194262X.2011.575628
  4. Shao, H. Q., Wei, H., He, J. H., “Dynamic properties and tire performances of composites filled with carbon nanotubes”, Rubber Chemistry and Technology, Vol. 91, No. 3, (2018), 609-620. https://doi.org/10.5254/rct.18.82599
  5. Novoselov, K. S., Geim, A. K., Morozov, S. V., Jiang, D., Katsnelson, M. I., Grigorieva, I. V., Dubonos, S. V., Firsov, A. A., “Two-dimensional gas of massless Dirac fermions in graphene”, Nature, Vol. 438, No. 7065, (2005), 197-200. https://doi.org/10.1038/nature04233
  6. Sawangphruk, M. Srimuk, P., Chiochan, P., Sangsri, T., Siwayaprahm, P., “Synthesis and antifungal activity of reduced graphene oxide nanosheets”, Carbon, Vol. 50, No. 14, (2012), 5156-5161. https://doi.org/10.1016/j.carbon.2012.06.056
  7. Meyer, J. C., Geim, A. K., Katsnelson, M. I., Novoselov, K. S., Obergfell, D., Roth, S., Girit, C., Zettl, A., “On the roughness of single-and bi-layer graphene membranes”, Solid State Communications, Vol. 143, No. 1-2, (2007), 101-109. https://doi.org/10.1016/j.ssc.2007.02.047
  8. Raadi, Z., Rahimi, A., Ghanbari, H., Sarpoolaky, H., “2D Materials; Introduction, Classifications, Properties, and Applications”, Journal of Advanced Materials and Technologies, 10, No. 4, (2022), 37-75. https://doi.org/10.30501/jamt.2021.260205.1145
  9. Moniri Javadhesari, S., Jabraili, M., Koohi, M., “A Review on the Application of Nanoparticles for Targeted Gene Delivery”, Advanced Ceramics Progress, Vol. 8, No. 1, (2022), 44-55. https://doi.org/10.30501/acp.2022.345741.1091
  10. Selvam, J. D. R., Smart, D. R., Dinaharan, I., “Microstructure and some mechanical properties of fly ash particulate reinforced AA6061 aluminum alloy composites prepared by compocasting”, Materials and Design, Vol. 49, (2013), 28-34. https://doi.org/10.1016/j.matdes.2013.01.053
  11. Reyhani, A., Mortazavi, S. Z., NozadGolikand, A., Moshfegh, A. Z., Mirershadi, S., “The effect of various acids treatment on the purification and electrochemical hydrogen storage of multi-walled carbon nanotubes”, Journal of Power Sources, Vol. 183, No. 2, (2008), 539-543. https://doi.org/10.1016/j.jpowsour.2008.05.039
  12. Liu, W. W., Xia, B. Y., Wang, X. X., Wang, J. N., “Exfoliation and dispersion of graphene in ethanol-water mixtures”, Frontiers of Materials Science, Vol. 6, (2012), 176-182. https://doi.org/10.1007/s11706-012-0166-4
  13. Ibrahim, K. S., “Carbon nanotubes-properties and applications: a review”, Carbon Letters, Vol. 14, No. 3, (2013), 131-144. http://doi.org/10.5714/CL.2013.14.3.131
  14. Dresselhaus, M. S., Lin, Y. M., Rabin, O., Jorio, A., Souza Filho, A. G., Pimenta, M. A., Saito, R., Samsonidze, G., Dresselhaus, G., “Nanowires and nanotubes”, Materials Science and Engineering: C, Vol. 23, No. 1-2, (2003), 129-140. https://doi.org/10.1016/S0928-4931(02)00240-0
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