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International Journal of Bioprinting                  High-performance SrCS scaffolds via vat photopolymerization

























            Figure 2. SEM images, element distribution, and particle size distributions of (a–b) SrCS powders, and (c–d) SrCS-40BTA composite powders.

            be difficult to fabricate the green body by VPP due to the   energy should allow the curing depth 2–3 times as thick as
            ceramic suspensions with ideal viscosity below 3 Pa·s at a   the sliced layer, which can ensure excellent layer-to-layer
            high shear rate for deposition and stereolithography [44-46] .   bonding to prevent cracking during sintering. However,
            Therefore, we selected SrCS-BTA ceramic suspensions with   the excess exposure energy would cause poor forming
            a solid loading of 40 vol.% and a viscosity less than 1 Pa·s at   accuracy. Therefore, based on the Beer–Lambert model, the
            a shear rate of 100 s  for VPP process (shown in Figure 3b).   exposure energy of 9, 20, 28, and 32 mJ/cm  were selected
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               We investigated the UV light absorption of SrCS-BTA   for curing SrCS, SrCS-20BTA, SrCS-30BTA, and SrCS-
            composite powders. As shown in Figure 4a, the SrCS-BTA   40BTA suspensions, and the corresponding curing depth
            composites revealed a strong UV light absorption at a   is shown in Table 1, respectively. In addition, the exposure
                                                               accuracy test also shows that the selected exposure energy
            wavelength below 350 nm, while the absorption decreased   is appropriate (shown in Figure S2 in Supplementary File).
            substantially at a wavelength of 350–400 nm. Therefore, the
            405 nm wavelength of the UV source was selected to cure   Further, we evaluated the UV-curing kinetics of
            the SrCS-BTA ceramic suspensions. Exposure energy is the   ceramic suspensions by tracking the absorption intensity
            most principal factor for VPP, which directly determines   of the C=C bond (shown in  Figure 4c). Upon UV
            the curing depth and forming precision of samples . As   irradiation, the unsaturated C=C bonds of HDDA reacted
                                                     [40]
            shown in Figure 4b, the curing depth varied linearly with   with  free  radicals  from the  dissociation  of  TPO  and
            LnE , and the slope of the fitting equation (D ) gradually   transformed into saturated single bonds . Therefore, the
                                                                                               [47]
               i
                                                 p
            decreased with increasing BTA content. Therefore, as the   infrared absorption intensity of unsaturated C=C bonds
            BTA content increased, more exposure energy was required   gradually weakened with the curing reaction. The infrared
            for a certain curing depth. Generally, the desired exposure   absorption intensity at around 1636 cm-1 was attributed



















            Figure 3. Viscosities of (a) SrCS suspensions with different solid loading and (b) 40 vol.% SrCS suspensions with different BTA contents at variable shear
            rates of 0–1000 s  and a constant shear rate of 100 s .
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            Volume 9 Issue 6 (2023)                        528                          https://doi.org/10.36922/ijb.1233
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