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Materials Science in Additive Manufacturing                          Alumina platelets additive manufacturing

























                               Figure 3. Fabrication process of the nacre-inspired samples for the three-point bending test.

            each print was 100 μm. The dimensions of the samples   First, the sintering temperature at 1600°C did not fully
            for bending test measure 45 mm × 3 mm × 4 mm. In the   densify the printed part, which resulted in poor or little
            second part of this study, we sintered the samples at 1600°C   bonding between the alumina platelets and nanoparticles.
            before infiltration.                               Moreover, the presence of nanoparticles between the
              Figure 4A illustrates a simple three-point bending test   platelets also prevented a full densification of the printed
            with the applied load perpendicular to the aligned platelets   part. Furthermore, obtaining a fully dense part would likely
            until failure. The flexural stress and strain (Figure 4B) were   restrict the infiltration of a secondary phase. Nevertheless,
            then calculated from the applied load and displacement   sintering at a higher temperature or reducing the amount
            with Equations II and III, respectively.           of nanopowder may improve the flexural strength of the
                                    3FL                        part due to greater mass diffusion and, hence, sintering of
                                 s=                    (II)    the powders.
                                    2bd 2
                                                                 The second reason for the low strength is due to the type
                                                               of polymer used for the secondary phase. Aside from the
                                    6Dd
                                 ε =  2                                    (III)  weaker mechanical properties of HDDA, we suspect that
                                     L                         the weak interfacial bonding between the alumina phase
              Observations from the composite (Figure  4C) under   and the polymer phase led to the peeling of the platelets.
            the SEM revealed several types of defects that contributed   This failure mode is shown in Figure 4D and F. In general,
            to the failure of the sample, as depicted in Figure 4D–F.   the  interface  damage  mechanism  is  governed  by  the
            The majority of these defects included platelets pull-out,   attraction forces to polymer chains from the alumina phase
            platelets peeled away from the polymer phase, and severed   19. When compared to the polymer phase, these attraction
            bridges that formed from the sintering of the nanoparticles.   forces from the alumina phase to the polymer chains
            The absence of fractured platelets suggests that only  the   are found to be weaker. Therefore, this weak interfacial
            platelet-polymer interface and bridges sustained the load,   bonding possibly served as a preferential manner of energy
            which contributed to the flexural strength of the composite.   dissipation and failure when loaded despite there being no
            However, since the flexural strength of  the HDDA was   obvious defects at the interface, as shown in Figure 2F.
            reported to be approximately 20 MPa, the calculated stress of
            more than 50 MPa suggested that there are other toughening   The last probable cause of the weak composite is
            mechanisms.  For instance, in addition to the energy   attributed to the defects from additive manufacturing, such
                      19
            dissipation from the fracturing of the bridges, cracks from   as delamination between layers. The delamination between
            the polymer phase could be seen deflected by the platelets   layers would create huge pores in the part after sintering,
            in Figure 4F, which prevented crack propagation directly   which would then be filled with the polymer, as depicted in
            through the sample. According to the bending tests, the   Figure 4G. This resulted in a composite consisting more of a
            fabrication of this composite based on the above-described   weaker polymer, hence lowering the strength. Furthermore,
            additive manufacturing method yielded a strength lower   the greater surface contact area between the polymer
            than expected. We consider a couple of factors that may   and ceramic phase as a result of this defect also offered
            have contributed to the low flexural strength.     a preferential location for failure, such as peeling of the


            Volume 3 Issue 1 (2024)                         6                       https://doi.org/10.36922/msam.2711
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