Tailoring graphene reinforced thermoset and biothermoset composites

2020 ◽  
Vol 36 (5) ◽  
pp. 623-652 ◽  
Author(s):  
Nur Bazilah Thalib ◽  
Siti Noor Hidayah Mustapha ◽  
Chong Kwok Feng ◽  
Rohani Mustapha

AbstractThe surge of knowledge among researchers pertaining to the excellent properties of graphene has led to the utilisation of graphene as a reinforced filler in polymer composites. Different methods of graphene preparation, either bottom-up or top-down methods, are important requirements of starting materials in producing reinforced properties in the composites. The starting graphene material produced is either further functionalised or directly used as a filler in thermoset polymer matrixes. An effective interaction between graphene and polymer matrixes is important and can be achieved by incorporating graphene into a thermoset polymer matrix through melt mixing, solution mixing or in situ polymerisation processes. In addition, by taking into consideration the importance of green and sustainable composites, the details of previous work on graphene reinforced bio-thermoset polymer matrixes is discussed. The resultant mechanical and thermal properties of the composites were associated to the chemical interaction between the graphene filler and a thermoset matrix. Exploration for further variations of graphene polymer composites are discussed by taking the reinforcement properties in graphene composite as a starting point.

e-Polymers ◽  
2010 ◽  
Vol 10 (1) ◽  
Author(s):  
Alexander Tolstov ◽  
Vitaliy Matyushov ◽  
Dmytro Klymchuk

AbstractThe novel approach for in situ preparation of polymer/TiO2 composites via low-temperature in-matrix crystallization of sol-gel prepared titania was developed and successfully applied. Rigid aromatic polyimide (PI) and flexible poly(ether-urethane)acrylate (PEUA) were used as polymer matrices and the templates for titania crystallization. Structure and morphology of prepared hybrids have been characterized by WAXD, FTIR and SEM. Chemical interaction between functional groups of the polymers and reactive inorganic component were studied. It was found that the rigid PI is more perspective matrix (instead of flexible PEUA) for carrying out the low-temperature crystallization of TiO2. Developed crystallization technique allowed to decrease the temperature of TiO2 crystallization from 350-500 °C to 250 °C (at atmosphere pressure) and to prepare functional crystalline TiO2-based polymer composites as perspective photoactive materials. Moreover, proposed approach gives also the possibility to obtain the polymer composites with enhanced compatibility between dispersed titania and continuous polymer phases.


2021 ◽  
Vol 594 ◽  
pp. 531-539
Author(s):  
Liang Wu ◽  
Shaozhuan Huang ◽  
Wenda Dong ◽  
Yan Li ◽  
Zhouhao Wang ◽  
...  

2021 ◽  
pp. 096739112110080
Author(s):  
Yelda Meyva Zeybek ◽  
Cevdet Kaynak

The main purpose of this study was to investigate influences of three parameters on the mechanical and thermal properties of the polylactide (PLA) matrix nanocomposites filled with polyhedral oligomeric silsesquioxane (POSS) particles. For the first parameter of “Filler Content”, nanocomposites with 1, 3, 5, 7 wt% basic POSS structure were compared. For the second parameter of “Functional Group,” basic POSS structure having only nonpolar isobutyl groups were compared with three other functionalized POSS structures; i.e. aminopropylisobutyl-POSS (ap-POSS), propanediolisobutyl-POSS (pd-POSS) and octasilane-POSS (os-POSS). Finally, for the third parameter of “Copolymer Compatibilization,” all specimens were compared before and after their maleic anhydride (MA) grafted copolymer compatibilization. Specimens were produced with twin-screw extruder melt mixing and shaped under compression molding. Various tests and analyses indicated that the optimum filler content for the improved mechanical properties was 1 wt%; while the optimum structure for strength and modulus was pd-POSS structure, in terms of fracture toughness it was basic POSS structure. Additional use of MA compatibilization was especially effective for the basic POSS and os-POSS particles.


Materials ◽  
2021 ◽  
Vol 14 (12) ◽  
pp. 3198
Author(s):  
Justyna Frączyk ◽  
Sylwia Magdziarz ◽  
Ewa Stodolak-Zych ◽  
Ewa Dzierzkowska ◽  
Dorota Puchowicz ◽  
...  

It was shown that carbon nonwoven fabrics obtained from polyacrylonitrile fibers (PAN) by thermal conversion may be modified on the surface in order to improve their biological compatibility and cellular response, which is particularly important in the regeneration of bone or cartilage tissue. Surface functionalization of carbon nonwovens containing C–C double bonds was carried out using in situ generated diazonium salts derived from aromatic amines containing both electron-acceptor and electron-donor substituents. It was shown that the modification method characteristic for materials containing aromatic structures may be successfully applied to the functionalization of carbon materials. The effectiveness of the surface modification of carbon nonwoven fabrics was confirmed by the FTIR method using an ATR device. The proposed approach allows the incorporation of various functional groups on the nonwovens’ surface, which affects the morphology of fibers as well as their physicochemical properties (wettability). The introduction of a carboxyl group on the surface of nonwoven fabrics, in a reaction with 4-aminobenzoic acid, became a starting point for further modifications necessary for the attachment of RGD-type peptides facilitating cell adhesion to the surface of materials. The surface modification reduced the wettability (θ) of the carbon nonwoven by about 50%. The surface free energy (SFE) in the chemically modified and reference nonwovens remained similar, with the surface modification causing an increase in the polar component (ɣp). The modification of the fiber surface was heterogeneous in nature; however, it provided an attractive site of cell–materials interaction by contacting them to the fiber surface, which supports the adhesion process.


2021 ◽  
Vol 79 (3) ◽  
pp. 121-147
Author(s):  
George Veronis

Hydrographic station data, consisting principally of temperature and salinity determinations, have been used by physical oceanographers to develop a climatological picture of the distribution of these quantities in the oceans of the world. Density as determined by Knudsen's formula, taken together with hydrostatic and geostrophic dynamics, also provides a crude picture of oceanic flow. However, the data probably contain substantially more information than has been derived from them in the past.The quantity that is orthogonal to potential-density curves in the S plane is suggested as a useful variable to complement the information contained in potential density. The derivation of this quantity, denoted by τ in this paper, is straightforward. A polynomial expression for τ that is suitable for computer calculations of τ from hydrographic station data is given. Shown are examples of hydrographic station data from the Atlantic plotted on the τσ diagram. The information contained in the τσ diagram shows many of the features exhibited in the TS plane. Vertical sections of τ appear to provide information about mixing in different parts of the Atlantic. The distribution of τ for abyssal waters at selected stations in the oceans of the world resembles the distribution of abyssal density as plotted by Lynn and Reid (1968). From the data presented, it appears that τ may serve as a good tracer for abyssal water movements.Since τ is defined to be orthogonal to σ, the expectation is that τ is a dynamically passive variable. However, since σ does not correlate with abyssal densities, it appears to lose dynamical significance at great depth, and τ assumes dynamical significance because of its orthogonality to σ. This unexpected feature leads to an exploration of the dynamical significance of σ. A natural starting point is the question of stability of abyssal water.A distinction is made between stability as determined by in situ determinations and as determined by the potential-density (σ) distribution. Simple examples are presented to show that analysis based on σ alone can lead to incorrect conclusions about gravitational stability of the water in the abyssal ocean. The reason is that seawater is a multicomponent thermodynamic system, and the thermodynamic coefficients are functions of pressure, salinity, and temperature. This functional dependence leads to adjustments in density as a water particle moves adiabatically in the vertical direction so that a layer of water that appears to be unstable near the surface may be stable (as determined by in situ determination) at great depth. A local potential density, which is simply the vertical integral of the in situ stability, is derived. This quantity gives a precise picture of gravitational stability in the vertical direction. Some distributions of local potential density are shown.Originally published May 15, 1972, in the Journal of Marine Research 30(2), 227???255.


Nanomaterials ◽  
2018 ◽  
Vol 8 (11) ◽  
pp. 894 ◽  
Author(s):  
Hongjiao Lin ◽  
Hejun Li ◽  
Qingliang Shen ◽  
Xiaohong Shi ◽  
Tao Feng ◽  
...  

An in-situ, catalyst-free method for synthesizing 3C-SiC ceramic nanowires (SiCNWs) inside carbon–carbon (C/C) composites was successfully achieved. Obtained samples in different stages were characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), and Raman scattering spectroscopy. Results demonstrated that the combination of sol-gel impregnation and carbothermal reduction was an efficient method for in-situ SiCNW synthesis, inside C/C composites. Thermal properties and mechanical behaviors—including out-of-plane and in-plane compressive strengths, as well as interlaminar shear strength (ILLS) of SiCNW modified C/C composites—were investigated. By introducing SiCNWs, the initial oxidation temperature of C/C was increased remarkably. Meanwhile, out-of-plane and in-plane compressive strengths, as well as interlaminar shear strength (ILLS) of C/C composites were increased by 249.3%, 109.2%, and 190.0%, respectively. This significant improvement resulted from simultaneous reinforcement between the fiber/matrix (F/M) and matrix/matrix (M/M) interfaces, based on analysis of the fracture mechanism.


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