3.1.1 The discovery of brass
Table 1 Chemical composition of supporting components of Temples and Dian ornaments, obtained using the portable XRF spectrometer.
Table 1
Chemical composition of supporting components of Temples and Dian ornaments, obtained using the portable XRF spectrometer.
Sample | Composition (wt%) a |
Sn | Pb | Zn | Cu | Fe |
TBB-1 | 4.8 ± 0.1 | 3.1 ± 0.1 | 5.6 ± 0.1 | 80.3 ± 0.2 | 1.6 ± 0.3 |
TBB-2 | 5.2 ± 0.1 | 3.0 ± 0.5 | 7.7 ± 0.4 | 78.2 ± 0.4 | 1.7 ± 0.2 |
SD-1 | 4.0 ± 0.1 | 3.5 ± 0.3 | 5.2 ± 0.1 | 86.3 ± 0.2 | 1.2 ± 0.2 |
SD-2 | 4.2 ± 0.1 | 5.5 ± 0.7 | 6.2 ± 1.0 | 79.0 ± 1.9 | 0.8 ± 0.1 |
SD-3 | 4.2 ± 0.4 | 1.8 ± 0.1 | 5.4 ± 0.3 | 83.6 ± 2.3 | 0.8 ± 0.1 |
a: The average value of multiple test values due to the systematic error of the portable XRF device. |
Based on the rarity of cultural relics, the nondestructive XRF method was first selected for their analysis. In particular, all the metal wires on the back of the temples and Dian ornaments labeled TBB1, TBB2, SD1, SD2, and SD3 were scanned using a portable XRF spectrometer. The surface chemical composition of all the samples was similar in component proportions, and the results are given in Table 1. Among all the components, the copper content was predominant, being more than 78 wt%, followed by zinc (5.2–7.7 wt%). In addition, other elements such as tin, lead, and iron were detected on the surface of the wires. Among these elements, copper, tin and lead were the main components of Chinese ancient bronze wares, making part of Chinese ancient metal relics [32]. The iron concentration was found to be less than 2 wt%, which might have come from soil elements or impurities of raw ore during smelting. However, zinc was very rare in ancient metalworks. According to the literature, zinc smelting technology was first dated to only the Ming dynasty epoch in China, condensing that the appropriate equipment hadn't been invented before this historical period. Although brass was discovered earlier than elemental zinc and thus became technically feasible[33], the method of smelting brass with copper and zinc in China had been unknown until the Ming dynasty period, according to the unearthed relics [34]. Up to now, only a few brass products related to a historical period of the Sui to Tang dynasty have been found in the Central Plains. Therefore, the presence of zinc in metal wares of the late Sui dynasty in Xi'an was unexpected, and further research was needed to verify whether this element was indeed making part of the above relics.
3.1.2 The determination of brass
To obtain the internal composition information about the copper alloy, the cross-sections of S1, S2, and S3 were probed via SEM-EDS technique.
Figure 2 (a) Cross-sectional BSE images of S1 sample. (b) Severe corrosion area at the edge of the cross-section. (c) Environmentally unaffected area at the center of the cross-section. (d) Grayish-white agglomeration areas in the cross-section. (e) Bright white particles in the cross-section. (f) Corrosion grain boundaries in the cross-section.
Table 2 Cross-sectional EDS results for S1 sample.
Table 2
Cross-sectional EDS results for S1 sample.
Analyzed area | Average composition |
Cu | | Zn | | Sn | | Fe | | Pb | | S | | O | | Cl | |
| wt% | at% | wt% | at% | wt% | at% | wt% | at% | wt% | at% | wt% | at% | wt% | at% | wt% | at% |
A (Fig. 2a) | 83.7 | 85.3 | 11.3 | 11.2 | 3.8 | 2.1 | 1.3 | 1.5 | | | | | | | | |
B (Fig. 2c) | 82.4 | 84.2 | 12.1 | 12.0 | 4.2 | 2.3 | 1.3 | 1.5 | | | | | | | | |
C (Fig. 2e) | 82.2 | 83.8 | 12.6 | 12.5 | 3.4 | 1.8 | 1.2 | 1.4 | | | | | | | | |
D (Fig. 2f) | 83.8 | 85.4 | 12.0 | 11.8 | 3.6 | 2.0 | 1.6 | 1.9 | | | | | | | | |
E (Fig. 2a) | 80.7 | 82.8 | | | 8.6 | 4.7 | 10.7 | 12.5 | | | | | | | | |
F (Fig. 2b) | 92.2 | 94.9 | | | 6.5 | 3.6 | 1.4 | 1.6 | | | | | 22.5 | 54.3 | 0.5 | 0.5 |
G (Fig. 2a) | 2.9 | 0.8 | | | | | | | | | | | 90 | 95.8 | 7.1 | 3.4 |
H (Fig. 2d) | 15.1 | 21.8 | | | | | | | 68.1 | 30.1 | 16.9 | 48.2 | | | | |
I (Fig. 2e) | 6.8 | 18.7 | 1.1 | 2.9 | | | | | 92.2 | 78.3 | | | | | | |
J (Fig. 2f) | 87.1 | 89.3 | 6.4 | 6.4 | 5.4 | 3.0 | 1.1 | 1.3 | | | | | | | | |
Cross-sectional BSE images of the S1 sample and the corresponding EDS results are shown in Figs. 2a-2f and Table 1. Since the area marked G in Fig. 2a was found to be composed of copper, chlorine, and oxide, this indicated that it was seriously eroded by soil elements under a long-term burial environment, and the corrosion products were mainly chlorides and oxides of copper [35]. To eliminate the influence of soil elements, the central regions labeled A, B, C, and D of the cross-section were analyzed. The components of A, B, C, and D were consistent with each other, being copper, zinc, tin, and a small amount of iron. The content of zinc was 12 wt% and that of tin was 3–4 wt%, meaning that the copper wire had a tin brass structure [36]. The iron content was stable across different areas, arising presumably from impurities in the smelting ore raw material.
Several grey regions (denoted as E in Fig. 2a and F in Fig. 2b) located between the severely corroded parts and the center of the cross-section were also examined. And their main elements were copper, iron, and tin. Zinc was not detected in these areas as compared to the central part of the cross-section. In the long-term burial environment, the metallic elements in cultural relics had been undergoing electrochemical reactions, leading to selective corrosion of the components, and the active elements in the alloy were more likely to be corroded and dissolved [37]. In brass, zinc is easy to be dissolved by preferential corrosion [38]. Therefore, E and F areas were formed by dezincification corrosion. With the increase of corrosion rate, tin was also corroded and dissolved. Finally, only the residual copper corrosion products (oxides and chlorides of copper) were detected in region D. Furthermore, compared with a central region of the cross-section under examination, the dezincification corrosion led to zinc depletion at the grain boundary marked J in Fig. 2f. Therefore, the elemental analysis of J, E, and F areas suggested that the corrosion of the cross-section diffused from the surface to the interior along the grain boundaries [39].
Many bright white particles denoted I in Fig. 2e were observed in the cross-section. The main components of the particles were copper and lead, with a small amount of zinc, indicating that the lead existed in the alloy in the form of particles. The gray-white agglomerations marked H in Fig. 2d were accumulated at the corroded grain boundaries of the sample, being composed of mainly copper, lead, and sulfur. Presumably, the brass contained trace amounts of sulfur, and lead aggregated near the copper-zinc sulfide in the form of particles[28]. When brass was corroded, the zinc in the copper-zinc sulfide was lost due to dezincification corrosion. And in the oxygen-free state, the affinity of lead to sulfur was greater than that of copper to sulfur, so the gray-white lead sulfide was formed and accumulated near the corrosion products.
Figure 3 Cross-sectional BSE images for: (a), (b) S2 and (c), (d) S3 samples.
Table 3 Cross-sectional EDS results obtained on S2 and S3 samples.
Table 3
Cross-sectional EDS results obtained on S2 and S3 samples.
Analyzed area | Average composition |
Cu | | Zn | | Sn | | Fe | | Pb | | S | | Cl | |
| wt% | at% | wt% | at% | wt% | at% | wt% | at% | wt% | at% | wt% | at% | wt% | at% |
A (Fig. 3a) | 83.6 | 84.9 | 12.5 | 12.3 | 2.9 | 1.6 | 1.0 | 1.2 | | | | | | |
B (Fig. 3b) | 83.4 | 84.9 | 12.0 | 11.9 | 3.4 | 1.8 | 1.2 | 1.4 | | | | | | |
C (Fig. 3c) | 84.0 | 85.7 | 10.7 | 10.6 | 4.0 | 2.2 | 1.4 | 1.6 | | | | | | |
D (Fig. 3d) | 82.8 | 84.2 | 12.4 | 12.2 | 3.2 | 1.8 | 1.6 | 1.9 | | | | | | |
E (Fig. 3c) | 98.5 | 97.3 | | | | | | | | | | | 1.5 | 2.7 |
F (Fig. 3c) | 91.2 | 93.8 | | | 6.6 | 3.6 | 2.2 | 2.6 | | | | | | |
G (Fig. 3d) | 92.8 | 94.0 | 3.7 | 3.6 | 2.9 | 1.6 | 0.7 | 0.8 | | | | | | |
H (Fig. 3d) | 9.9 | 14.9 | 1.6 | 2.4 | 3.2 | 2.6 | | | 69.4 | 32.3 | 15.9 | 47.9 | | |
I (Fig. 3b) | 13.3 | 32.4 | 2.0 | 4.6 | | | | | 84.7 | 78.3 | | | | |
Figure 3 and Table 3 display the SEM-EDS results acquired on the cross-sections of S2 and S3 samples. The four BSE images in Fig. 3 include the matrix regions corresponding to the uncorroded zone, the section with copper corrosion products formed by the environmental corrosion, the dezincification area, and the lead sulfide accumulated domain, respectively. The central area of the copper wire, which was less affected by the environment, was composed of copper, tin, zinc, and lead particles. According to these data, S2 and S3 were made of tin brass, which was consistent with S1 sample. Therefore, the supporting parts of the coronet were all of brass which was the first confirmation of the brass application in the Central Plains during the Sui-Tang-dynasty period. Moreover, the brass products exhibited their uniform composition without obvious segregation, which might be the new evidence that brass smelting technology was at a stage of steady development in the Sui-Tang-dynasty epoch.
3.1.3 Production process
Figure 4 Optical micrographs and SEM images showing the cross-sectional metallographic structure of S1 sample. (a) The structure consisting of twinned α-grains. (b) Grains at the edge filled with numerous slip lines, indicating that the sample was given multiple mechanical treatments. (c) Lead particles and lead sulfide (PbS). (d) Slip lines.
The metallographic structure was obtained, as shown in the Fig. 4. The zinc content of brass was stable at 12 wt%, and the microstructure of brass at room temperature was composed of single-phase α-copper-zinc solid solution (see in Fig. 4a), consisting exclusively of twinned α grains, which was an unmistakable indication of thermomechanical treatment applied to the sample [40]. α-phase brass had excellent mechanical properties due to its good plasticity and ability to withstand hot and cold processing. In Fig. 4b, grains at the edge of the sample were filled with numerous slip lines in different directions, which indicated that the sample underwent multiple cold processing in different directions [41]. Lead particles were randomly distributed in the cross-section, and lead sulfide (PbS) emerged at the Cu-Zn grain boundaries where the dezincification corrosion occurred [42]. The brass was assumed to be processed by integral hot forging into brass wires with diameters of 2 mm, which were afterwards fixed on the crown after surface cold shaping such as cutting and hammering during the production of the supporting parts.