Sara Tahan Latibari

Synthesis, mechanical properties, and in vitro biocompatibility with osteoblasts of calcium silicate-reduced graphene oxide composites.

Calcium silicate (CaSiO3, CS) ceramics are promising bioactive materials for bone tissue engineering, particularly for bone repair. However, the low toughness of CS limits its application in load-bearing conditions. Recent findings indicating the promising biocompatibility of graphene imply that graphene can be used as an additive to improve the mechanical properties of composites. Here, we report a simple method for the synthesis of calcium silicate/reduced graphene oxide (CS/rGO) composites using a hydrothermal approach followed by hot isostatic pressing (HIP). Adding rGO to pure CS increased the hardness of the material by ∼40%, the elastic modulus by ∼52%, and the fracture toughness by ∼123%. Different toughening mechanisms were observed including crack bridging, crack branching, crack deflection, and rGO pull-out, thus increasing the resistance to crack propagation and leading to a considerable improvement in the fracture toughness of the composites. The formation of bone-like apatite on a range of CS/rGO composites with rGO weight percentages ranging from 0 to 1.5 has been investigated in simulated body fluid (SBF). The presence of a bone-like apatite layer on the composite surface after soaking in SBF was demonstrated by X-ray diffraction (XRD) and field emission scanning electron microscopy (FESEM). The biocompatibility of the CS/rGO composites was characterized using methyl thiazole tetrazolium (MTT) assays in vitro. The cell adhesion results showed that human osteoblast cells (hFOB) can adhere to and develop on the CS/rGO composites. In addition, the proliferation rate and alkaline phosphatase (ALP) activity of cells on the CS/rGO composites were improved compared with the pure CS ceramics. These results suggest that calcium silicate/reduced graphene oxide composites are promising materials for biomedical applications.

Mechanical and in vitro biological performance of graphene nanoplatelets reinforced calcium silicate composite.

Calcium silicate (CaSiO3, CS) ceramic composites reinforced with graphene nanoplatelets (GNP) were prepared using hot isostatic pressing (HIP) at 1150°C. Quantitative microstructural analysis suggests that GNP play a role in grain size and is responsible for the improved densification. Raman spectroscopy and scanning electron microscopy showed that GNP survived the harsh processing conditions of the selected HIP processing parameters. The uniform distribution of 1 wt.% GNP in the CS matrix, high densification and fine CS grain size help to improve the fracture toughness by ∼130%, hardness by ∼30% and brittleness index by ∼40% as compared to the CS matrix without GNP. The toughening mechanisms, such as crack bridging, pull-out, branching and deflection induced by GNP are observed and discussed. The GNP/CS composites exhibit good apatite-forming ability in the simulated body fluid (SBF). Our results indicate that the addition of GNP decreased pH value in SBF. Effect of addition of GNP on early adhesion and proliferation of human osteoblast cells (hFOB) was measured in vitro. The GNP/CS composites showed good biocompatibility and promoted cell viability and cell proliferation. The results indicated that the cell viability and proliferation are affected by time and concentration of GNP in the CS matrix.

From rice husk to high performance shape stabilized phase change materials for thermal energy storage

A novel shape-stabilized phase change material (SSPCM) was fabricated by using a vacuum impregnation technique. The lightweight, ultra-high specific surface area and porous activated carbon was prepared from waste material (rice husk) through the combination of an activation temperature approach and a sodium hydroxide activation procedure. Palmitic acid as a phase change material was impregnated into the porous carbon by a vacuum impregnation technique. Graphene nanoplatelets (GNPs) were employed as an additive for thermal conductivity enhancement of the SSPCMs. The attained composites exhibited exceptional phase change behavior, having a desirable latent heat storage capacity of 175 kJ kg−1. When exposed to high solar radiation intensities, the composites can absorb and store the thermal energy. An FTIR analysis of the SSPCMs indicated that there was no chemical interaction between the palmitic acid and the activated carbon with GNPs. The thermal conductivity of the prepared composites improved by more than 97% for the highest loading of GNPs (6 wt%) compared with that of pure palmitic acid. Moreover, the SSPCMs exhibit high thermal stability, with a stable melting–freezing enthalpy and excellent reversibility. The prepared SSPCMs with enhanced heat transfer and phase change properties provide a beneficial option for building energy conservation and solar energy applications owing to the low cost of raw materials and the simple synthetic technique.

Facile Preparation of Carbon Microcapsules Containing Phase-Change Material with Enhanced Thermal Properties

This study describes the hydrothermal synthesis of a novel carbon/palmitic acid (PA) microencapsulated phase change material (MEPCM). The field emission scanning electron microscopy (FESEM) and high resolution transmission electron microscopy (HRTEM) images confirm that spherical capsules of uniform size were formed with a mean diameter of 6.42 μm. The melting and freezing temperature were found to be slightly lower than those of pure PA with little undercooling. The composite retained 75% of the latent heat of pure PA. Thermal stability of the MEPCM was found to be better than that of pure PA. The thermal conductivity of MEPCM was increased by as much as 41% at 30°C. Due to its good thermal properties and chemical and mechanical stability, the carbon/PA MEPCM displays a good potential for thermal energy storage systems.

Investigation of fracture toughness parameters of epoxy nanocomposites for different crack angles

Abstract The effects of single-walled carbon nanotubes (SWCNTs) on the mechanical properties of nanocomposites with epoxy matrix were studied, with the emphasis on fracture toughness under tensile loading conditions. It has been demonstrated that adding CNTs into polymer-based materials can improve the mechanical properties of this material. CNTs possess a certain potential to improve the fracture toughness of epoxy systems due to their mechanical properties and increase the fracture toughness of nanocomposites. Since the fracture toughness parameters were best manifested in the scaling properties and were the main parameters, the angles of different cracks have been simulated in a 3D finite element framework and the effects of different angles of crack, on the fracture toughness of polymers, have been modeled and investigated. The simulations are run for different bias angles. The influence of angle, the crack lengths and the variations of different lengths of nanocomposite in different volume fractions (vol%) are investigated. That is to say, at first, nanocomposites had a significantly higher fracture toughness compared to the pure epoxy. We found that nanocomposites, in the presence of SWCNTs, had a greater effect on fracture toughness of nanocomposites in a greater volume of fractions. Also, the nanocomposites exhibited a significant increase in fracture toughness, with zero angle of crack compared with greater angles. In addition, it is found that at a constant volume fracture, fracture toughness, increases by increasing crack lengths.