Experimental Cremation of Bone: Crystallite Size and Lattice Parameter Evolution
In this study we investigate pristine and experimentally incinerated bovine bone material with differing annealing times and temperatures from 100 to 1000 °C to analyse the crystallographic change of natural bone mineral during cremation. We used X-ray powder diffraction (XRPD) and Fourier transform infrared (FTIR) spectroscopy as complementary methods. We observe a structural change of bone mineral during cremation. Our study highlights that there are only few or even no hydroxyl ions in pristine bone mineral (bioapatite), which is a carbonate-hydro-apatite rather than a hydroxyapatite. A significant recrystallization reaction from bioapatite to hydroxyapatite takes place at elevated temperatures from 700 °C (after 30 min cremation time). This process is associated with a significant increase of crystallite size, and it involves an increase of hydroxyl in the apatite lattice that goes along with a depletion of water and carbonate contents during cremation. Our first results highlight the importance of both time and temperature on the recrystallization reaction during cremation.
KeywordsCarbonated apatite Calcium phosphate Bioapatite Bone X-ray diffraction FTIR Rietveld refinement
The Forschergruppe FOR 1670 project on human transalpine mobility in the Late Bronze Age to Early Roman times performs isotope studies on archaeological bone finds. During that age, cremating the deceased was the primary burial custom (Grupe et al. 2015). To understand bone alteration by cremation, we study the evolution of bone crystallography and crystallite size as a function of cremation temperature and annealing time for bovine bone by FTIR and X-ray diffraction. Mammal bone mineral is a nanocrystalline material consisting of an apatite mineral that is chemically far more complex than hydroxyapatite and can be approximated as (Ca,Mg,Na)10-x((PO4)6-x(CO3)x)(OH1-y-z, (CO3)y, (H2O)z)2 (Elliott 2002; Rey et al. 2007). It comprises between 5 and 8 wt% carbonate, which substitutes in the [OH]− site (A-type substitution) as well as the [PO]43- site (B-type substitution) of the apatite structure (LeGeros et al. 1969; Wopenka and Pasteris 2005; Pasteris et al. 2012; Yi et al. 2013). Previous studies showed that recrystallization of the bioapatite and crystallite growth mainly sets in from about 600 °C (Piga et al. 2009; Schmahl et al. 2017), but small changes are already apparent at low temperatures of 100 °C (Harbeck et al. 2011). In this study, we want to define more precisely the cremation temperature and annealing time where hydroxyapatite crystallization sets in.
3.2 Materials and Methods
Pieces of compact bone were cut from the tubular part of bovine femur; the endosteal and periosteal surfaces were mechanically removed. Samples were ultrasonically washed in deionized H2O. After air-drying, the bones were defatted for 5 days with diethyl ether in a Soxhlet and air-dried. Finally, the samples were homogenized to a fine powder and passed through a 100 μm sieve.
Cremation experiments were carried out between 100 and 1000 °C in air (oxidizing conditions) in steps of 100 °C with 150 min annealing time. After data analysis of the initial results, we focussed on the temperatures of 650 and 700 °C and used shorter exposure times between 10 and 60 min in intervals of 10 min.
X-ray diffractograms were collected on a General Electric 3003 powder diffractometer in Bragg-Brentano reflection geometry. Cu-Kα1 radiation was selected with an exposure time of 1000s.
All samples were mixed with NIST 660b LaB6 as internal standard (2–5 wt%). The FULLPROF code (Rodríguez-Carvajal 1993; Rodríguez-Carvajal and Roisnel 2004) was applied for data evaluation and Rietveld refinement (Rietveld 1969). The Thompson-Cox-Hastings method for convolution of instrumental resolution with size and isotropic microstrain broadening (Thompson et al. 1987) was applied. For refinement, a hexagonal symmetry model for carbonated apatite was used (Wilson et al. 2004).
Infrared spectra were measured on a Bruker Equinox FTIR instrument with a resolution of 4 cm−1 with 128 scans.
3.3.1 X-Ray Diffraction: 100 °C Intervals
Exemplary Rietveld refinements of samples cremated at 600 °C and 700 °C for 150 min annealing time are shown in Fig. 3.1b, c. Enlarged images of the 31–35° 2θ section show overlapping apatite diffraction peaks in Fig. 3.1b, whereas peaks in Fig. 3.1c can clearly be distinguished from each other. The lattice parameters and crystallite sizes obtained by Rietveld refinement of diffractograms measured at room temperature for the 150 min heat-treated samples are shown in Fig. 3.1d, e. Note the sharp rise of the crystallite size setting in at 700 °C. The lattice parameters show an initial increase with annealing treatment and then sharply drop at temperatures where the grain size sharply increases.
3.3.2 X-Ray Diffraction: 10 Min Intervals
X-ray diffractograms of bovine bone cremated at 700 °C from 10 to 60 min show a broad diffraction peak shape from 10 to 30 min annealing time. Samples annealed for 40 min or longer depict sharper peaks. Bovine bone incinerated at 700 °C shows a steady increase of the crystallite size up to 30 min experimental cremation. From 30 to 40 min elapsing time, we observe a significant jump from 117.85(2) Å to 294.8(3) Å (2.5 times larger) (Fig. 3.2f). Moreover, we observe a decrease of lattice parameters a and c until 40 min annealing times. This trend is reversed after 50 min annealing (Fig. 3.2e, f).
Absorption bands at 873–879 cm−1 and 1400–1458 cm−1 were attributed to ν2CO32− and ν3CO32− (Fleet 2009; Grunenwald et al. 2014; Rey et al. 1989). The intensity of carbonate bands begins to decrease from 400 °C with increasing annealing temperatures and can barely be observed for the sample cremated at 1000 °C (see Fig. 3.3a). For untreated bovine bone, we observe broad H2O absorption bands from ~3000 to 3600 cm−1 (Brubach et al. 2005). These peaks lose intensity with heat treatment and disappear for the 700 °C and higher heat treatments (Fig. 3.3c).
The OH- stretch vibration gives a sharp peak at 3570 cm−1 (González-Díaz and Hidalgo 1976; González-Díaz and Santos 1977; Vandecandelaere et al. 2012). The band at ~632 cm−1 was assigned to the OH− libration mode (Destainville et al. 2003). In the untreated bone spectra and for low annealing temperatures, neither the OH− libration peak near 630 cm−1 nor the sharp and distinct OH− stretching vibration peak at 3570 cm−1 is present. However, these OH− signals emerge with annealing at 400 °C and significantly increase and become well-differentiated for samples annealed at temperatures of 700 °C or higher (see Fig. 3.3b, c).
In the original bone, we observe broad diffraction peaks (Figs. 3.1a and 3.2a, b) due to the nanoscale dimension of the bone apatite crystallites. Further, the high intensity of the carbonate and H2O vibration bands and absence of OH− bands quite clearly indicate that bone apatite is a carbonate-hydro-apatite rather than a hydroxyapatite (Fig. 3.3a–c). Loong et al. (2000) using inelastic neutron scattering and Pasteris et al. (2004) using Raman spectroscopy came to similar conclusions.
With extended annealing treatment, the diffraction peaks of the bone mineral get sharper; the (CO3)2− infrared signals decrease, while the OH− infrared peaks increase. Within the broad water band, one can clearly see the rising of the OH− stretching is a function of increasing annealing temperature (Fig. 3.3c). This indicates a reaction from bioapatite (carbonate-hydro-apatite) to hydroxyapatite with heat treatment, as the material approaches stoichiometric chemistry. This reaction is associated with growth of the crystallites; the growth becomes more rapid at temperatures from 700 °C and higher (Figs. 3.1a and 3.2d). At the same time, loss of carbonate and water and their replacement by OH− in the structure lead to a decrease of unit cell parameters (Figs. 3.1d, e and 3.2b–f).
While observing these structural changes occurring, it cannot be simply concluded that the process occurs homogeneously within the apatite lattice. It is just as likely that the bioapatite decomposes and that hydroxyapatite is formed in a heterogeneous reaction at the expense of the decomposing bioapatite. It must be borne in mind that our techniques integrate over the whole volume of the sample, and the diffraction peak positions as well as IR frequencies of both mineral phases (bioapatite and hydroxyapatite) are very close and initially severely broadened. Thus our techniques might well record a superposition of the signals of both phases coexisting. Here it is important to note that the distinct increase of the crystallite size for temperatures of and above 700 °C sets in after 30 min of annealing time (Fig. 3.2e, f). This may be indicative of a heterogeneous rather than a homogeneous reaction from bioapatite to hydroxyapatite. For an increase of crystallite size of only one homogeneous apatite phase by Ostwald ripening, the evolution of crystallite size with time (Fig. 3.2f) should have the opposite curvature than observed.
The time dependence (Fig. 3.2) of the reaction process becomes important when concluding from bone crystallinity to cremation temperature. Up to 40 min cremation time, we see the same trend for lattice parameters when comparing 650 and 700 °C: a decrease of lattice parameters a and c and therefore a shrinkage of the unit cell coupled with an increase of the crystallite size (Fig. 3.2b–f). After more than 30 min annealing at 700 °C, we see more rapidly increasing lattice parameters, an effect which is not observable in the 650 °C temperature experiments. Moreover, at 700 °C after 30 min annealing, we observe also a significant change in crystallite size which we attribute to a progressive recrystallization reaction of bioapatite to hydroxyapatite. At that time, the decomposition products (essentially carbon) of organics such as collagen, which comprise about 35 wt% of the original bone material (Rogers and Zioupos 1999), are almost completely gone, and the hydroxyapatite crystallites can grow without being impeded by films of organics or their residues which separate the crystallites.
Note that bone annealed at 400 °C for 150 min displays essentially the same crystallite sizes as bone treated for 20 min at 700 °C (~97 Å), and bone annealed at 600 °C for 150 min displays similar crystallite sizes as bone treated at 650 °C for 50 min (~133 Å). Our experiments reveal that it is important to consider the influence of time when concluding from material state on cremation conditions.
We thank the Deutsche Forschungsgemeinschaft (DFG) for funding the project in Forschergruppe FOR1670 under Schm930/12-1 and Gr 959/20-1,2.
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