The mechanical properties of various polymers are well known. The mechanical properties of FDM-printed test specimen have been investigated by tensile tests and differ from injection molded parts [7]. Since the main interest of this work was to investigate the layer adhesion of the printing process in absence and in presence of oxygen, test specimen was printed with the longest side orthogonal to the printing platform (and shortest side parallel to the moving direction of the platform) to maximize the number of layers. The influence of the printing direction on the mechanical properties has been analyzed in detail [8–10]. The print of the test specimen according to EN ISO 527-2 (type 1B) as long and thin objects orthogonal to the printing platform revealed certain difficulties [11]. Smaller test specimen (type 1BB, 30 × 2 × 2 mm) would result in a very small printed layer area (4 mm2). Consequently, test specimens were printed as small plates (30 × 10 × 3 mm). This leads to a layer area of 30 mm2 and allows a more reliable comparative investigation of the layer adhesion. As a consequence, absolute values reported here may not be compared directly to values derived from tensile tests of test specimen of a different geometry.
Figure 2 shows averaged load–strain curves obtained from the tensile tests of the printed plates made of ABS and nylon copolymer (Taulman 910) at air and inside the oxygen-free inert gas atmosphere of the glove box. At first sight, the increased elongation at break is obvious for ABS, while the nylon copolymer shows a significantly increased tensile strength and an increased elastic modulus.
The averaged results obtained from all tensile tests are summarized in Table 1. For plates made of natural ABS a significantly improved elongation at break from ε
B = 4.4 ± 1.5 % to 10.7 ± 2.6 % is obtained. This may be explained by a better layer adhesion of the FDM printed layers. The values for the elastic modulus and the tensile strength are generally quite identical and within the expected range for ABS before and after 3D printing [7, 12]. A slight improvement (+10 %) of the tensile strength is noted for the plates printed under a nitrogen atmosphere. As a comparison, printed test specimen of type 1BB results in an elastic modulus of E = 1.56 ± 0.07 kN mm−2 and a tensile strength of σ
M = 25.5 ± 0.9 N mm−2, which is in good accordance with results reported in literature [7].
Table 1 Summary of averaged results obtained from tensile tests of 3D-printed plates made of ABS and nylon copolymer (Taulman 910) at air and under an inert gas atmosphere
For the nylon copolymer Taulman 910, which is generally more extendible (tearing was not observed during the test conditions) a significant increase in tensile strength from σ
M = 36.0 ± 2.2 N mm−2 to 49.9 ± 13.8 N mm−2 is achieved under exclusion of water and oxygen. The tensile strength generally is in the range expected for the material [2]. Additionally, an increasing elastic modulus was observed (Table 1). Lowering the printing temperature for the dried nylon copolymer to 240 °C (as suggested by the manufacturer) led to a decrease of the tensile strength to σ
M = 33.6 ± 3.8 N mm−2 and to E = 1.01 ± 0.04 kN mm−2 (plates, inert gas). If the nylon copolymer was not dried before printing at air, the tensile strength is reduced to σ
M = 19.9 ± 2.2 N mm−2 and the elastic modulus to E = 0.60 ± 0.11 kN mm−2 (plates, air). This clearly shows the general influence of the water on the mechanical properties of nylon, which is a well-known fact. For all other prints at air and under the nitrogen atmosphere, a rigorous drying procedure of the nylon filament was applied.
For SLS, it is well known that the crystallinity of polyamides changes with the degree of particle melting, which strongly affects the mechanical properties [13, 14]. For polylactide (PLA), the influence of the extruder temperature on the crystallinity and mechanical properties has been investigated [15]. We compared the crystallinity of the nylon copolymer printed at air with samples printed under the inert gas atmosphere. At first look, the X-ray powder diffraction (XRD) measurements show slight differences at the typical signal of semicrystalline polyamide around 2Θ = 21° (see Fig. S4 of the supplementary material) [16]. With the help of differential scanning calorimetry (DSC) measurements, a higher crystallinity for the nylon plates printed at air was determined. According to the DSC measurements, the samples printed at air are 15 % more crystalline (roughly 20 % crystallinity) than the samples printed under a nitrogen atmosphere as shown in Fig. 3, which may explain the improved mechanical properties for prints performed under an inert gas atmosphere.
ABS is a purely amorphous polymer. As a consequence, crystallinity cannot be affected by the printing conditions. Accordingly, the XRD measurements of both samples are identical and in agreement with an amorphous polymer and the DSC heating curves do not show a melting peak (see Fig. S1 of the supplementary material). The second glass transition (T
g) of ABS is found around 110 °C, which is in accordance with the material properties. According to literature, the oxidation of the polybutadiene phase of ABS can be monitored by a large shift of the first glass transition, which is located around −65 °C, to significantly higher temperatures. Unfortunately, the first glass transition is rather broad and gets even broader upon oxidation and it was not possible to determine the first glass transition from the DSC measurements at low temperatures (see Fig. S2 of the supplementary material) [3]. In all cases, the printed plates made of ABS and nylon copolymer printed under inert gas conditions were pure white without the slightest discoloration, while all plates printed at air showed a slight yellow/brownish coloring in direct comparison. This is in accordance with the expected beginning of degradation of the polymers printed at air. Overall, at the current point it may be concluded that the suppression of oxidation processes leads to a better layer adhesion in case of ABS (leading to a higher elongation at break) while the extremely dry atmosphere may affect crystallization of the polyamide and is responsible for the improved tensile strength.