1. Introduction
The preservation of cultural heritage is directly related to the interaction of monuments with their surroundings. This includes the environmental conditions they are subjected to and also aspects of a social and economic nature [
1,
2,
3]. Considering the particular interaction of buildings with environmental conditions, the chemical and physical behavior of the materials used represents a key factor for the definition of preservation actions. It is known that climatic factors, such as wind, rainfall, changes in temperature and humidity, and pollutants, can accelerate processes of deterioration of materials in constant exposure to these factors, as is the case of built heritage [
4]. In the context of the HERACLES project, the analysis of the materials that constitute the chosen monuments/assets as a study case is part of a set of strategies aimed at promoting the resilience of this heritage facing climatic changes. In the case of the Town Walls in Gubbio, the study emphasis was given to the mortars.
Mortars can be used for different functions in a construction, such as a binding element of stone blocks, for filling the gap zones, or as a coating [
5,
6]. When used as a binding element between stone blocks, the physical and chemical integrity of this material is fundamental for maintaining the structure. The main objective of this study is to minerochemically and morphologically characterize the samples of mortars collected in different areas of the medieval walls of Gubbio, since understanding their characteristics can help to answer current issues that may contribute to the preservation strategies for this monument.
1.1. Lime Mortars
Mortars are complex materials, composed of the mix of a binder and aggregates, both inorganic raw materials, and may contain other additives, including organic materials [
7]. Several types of binders have been used historically. However, during the medieval period, the most common binder used was based on calcium carbonate (CaCO
3), obtained from stones rich in calcite. The process of preparation of the mortar involves the calcination and decomposition of calcite (CaCO
3) to lime (CaO). Portlandite [Ca(OH)
2], resulting from the hydration of the lime, was usually mixed with inorganic aggregates, typically sand in defined proportions, and water [
7,
8]. When applied, the carbonation process of Portlandite begins, through the reaction with atmospheric CO
2 conferring hardness and mechanical resistance to the material (aerial lime). If the process of hardening of the mortar occurs through reaction with water, the mortar is considered hydraulic. This type of material can be obtained from natural hydraulic lime or produced by adding grinded ceramics (
cocciopesto), ash, and pozzolan in nonhydraulic lime. However, the hydraulic properties of a mortar also depend on the preparation conditions of the material [
9]. The aggregates also have a relevant role in the performance of the material, its dimension, shape, and distribution in the binder matrix being important. In addition, in the case of air lime mortars, the environmental conditions of temperature, humidity, and the methods of preparation and application can be decisive for the process of carbonation of the mortar [
5,
10]. The use of both aerial and hydraulic lime mortars was widely disseminated in the Middle Ages, falling into disuse during the nineteenth century, after the development of Portland cement [
5,
9].
1.2. The Case Study: Gubbio Town Walls
Inserted in the urban landscape, the Town Walls of Gubbio are a fundamental part of the city. Archaeological remains indicate that the construction of the walls dates from before the medieval period and that at least part of its structure may have initially been built as a protection system of the village against the floods of the river Camignano [
11]. The Middle Ages were marked by the strong expansion of several cities in the central and northern regions of Italy, in which the expansion and adaptation of the walls assumed both the functions of defense of the village and urban planning [
12,
13]. Gubbio was an important city in the medieval period and its walls accompanied its development, mainly from the beginning of the 14th century, when the walls also played a protective role of the village against the attacks of enemies and invaders [
13]. The tracing of the medieval walls accompanied the old walls along the slope of Ingino Mount, in the N–NE direction. The extension located in the lower part corresponds to the expanded territory. The construction of this extension of the walls was completed before 1350 [
14] (
Figure 1).
The medieval town walls of Gubbio extend for 2.8 km. The dimensions are varied and can reach a height of 12.0 m at the highest point and a thickness ranging between 0.5 and 3.0 m. In addition, the walls of Gubbio include gates and a defense tower.
At least three types of stones were used in the construction of the oldest part of the walls, namely, limestone, travertine, and sandstone joined by mortar. The medieval walls also present apparent material differences, resulting from successive construction additions, reinforcement of the structure, and restoration/renovations that occurred over the centuries. For the HERACLES Project, five zones of the walls were chosen as the focus for sample collection and material characterization in the laboratory (ex-situ analysis). However, the materials collected in Zone 1 do not correspond to mortar samples, and therefore are not included in this study. The location of the sampling zones shown in
Figure 2 are: Zone 1—“Forte di Parco Ranghiasci”; Zone 2—“Cassero”; area between Zone 3—“Torre”—and Zone 4—“Porta S. Ubaldo”; area between Zone 4—“Porta S. Ubaldo”—and Zone 5—“Bughetto”; Zone 5—“Bughetto”.
It is estimated that the oldest part of the walls corresponds to Zone 1, completed in 1301. Zone 2, also built in the Middle Ages, underwent several changes in the late 14th and early 15th centuries and was largely destroyed in the nineteenth century. Zone 3 does not present signs of recent intervention. Zones 4 and 5 correspond to the same period of construction of Zone 1 but suffered the largest interventions in relation to the removal of accumulated land against the walls and actions of restoration and preventive conservation.
As referred before, the degree of preservation of the medieval walls is directly related to the surroundings and environmental conditions. Rainfall particularly affects the Town Walls of Gubbio due to its location in relation to the topography of the terrain, since it increases the transport of soil and rubble from the hillside, which eventually accumulates near the walls. Zones 3, 4, and 5 are the most affected, where the accumulation of soil along the walls causes an intensification of the pressure sustained by the structure, leading to a higher risk of collapse, especially in the most fragile parts. Furthermore, it also causes alteration in moisture retention and circulation within the materials constituting the walls, which can negatively affect the materials and contribute to the weakening of the structure. Another factor that should be considered is the presence of vegetation in the surrounding area, since it stimulates the growth of primary microorganisms, which develop in inorganic substrates, causing chemical and physical alterations in the materials. In the case of plant development in the wall structure, the roots can cause physical deterioration of mortars and stones.
Considering the abovementioned factors and the way they can affect mortars and compromise the structure of the walls, the materials’ morphological, mineralogical, and chemical characterization is an important step to determine its degree of conservation and also to define the future actions to preserve this heritage.
2. Materials and Methods
Mortars are materials composed of raw materials of a very diverse nature and with a composition that can vary considerably. This study was carried out using a set of ex-situ analytical techniques in samples collected in different areas of the medieval walls. The mortar samples were collected according to the period of construction and/or intervention, as shown in
Table 1.
For the morphological, mineralogical, and chemical characterization, a small portion of the samples were grinded with an agate mortar and pestle to perform chemical analysis or assembled in epoxy resin and mechanically polished (mainly for surface observation). A set of analytical techniques where preferentially used, such as optical microscopy (OM), X-ray diffraction (XRD), and X-ray fluorescence spectrometry in wavelength dispersive mode (WDXRF). Although these techniques require some sample preparation, such as grinding, after performing the measurements the samples are recovered, remaining available for conducting new tests, if necessary. Other methodologies used that do not allow sample recovery include scanning electron microscopy (SEM) and simultaneous thermogravimetry and differential thermal analysis (TG–DTA).
The direct observation of samples was done using an Olympus BX51 Optical Microscope with reflected light in darkfield observation mode. The polished section observation of samples was done using a reflected light (optical) microscope Leica DMI5000M, also in darkfield observation mode. The sample was also observed at the optical and metallurgical microscope (Nikon Epiphot TME).
SEM observation and EDS analysis for morphology and microstructure evaluation were performed by field emission scanning electron microscopy (FEG–SEM, Zeiss LEO Supra 35), coupled with energy dispersive spectroscopy (EDS) (INCAx-sight, Oxford instruments) on petrographic thin sections of mortars and/or stones. Samples were coated with a 10 nm thick chromium layer before observation.
XRD analyses for the identification of mineralogical phases were performed using a Rigaku Diffractometer, model DMAX III-C 3kW, with copper Kα radiation at 40 kV and 30 mA settings, in the 2θ range 10° to 65°, with a step of 0.08° and an acquisition time of 1 s, in continuous scan mode. The crystalline phase identification was done using the EVA software (DIFFRAC Plus EVA) [
16].
WDXRF analyses for samples’ elemental composition determination were performed using a 4.0 kW Panalytical Axios sequential spectrometer. Standardless semiquantitative analysis was performed under an He flow with the SuperQ IQ+ software package [
17].
Simultaneous TG–DTA for assessing the thermal behavior of the samples was performed with a Setaram TGDTA 92 apparatus using an Ar flow. The heating rate up to 1100 °C was 10°/min.
3. Results and Discussion
Considering the morphology of the material, the mortar samples show a great variation of granulometry of aggregates. Through optical microscopy, it was possible to note that two of the samples exhibit relatively homogeneous dimension of grains, approximately 75 µm (GTW 2 and GTW 4), well distributed in the binder matrix. The regular size of the grains can be related with the quality of the mortar and the homogeneous distribution of aggregates suggests a good mixing process during mortar preparation [
18]. However, for the remaining samples, the size, shape, and color of the grains are quite varied, as is the dispersion of aggregates in the binder. In general, the binder shows a pink homogeneous coloration but in some samples appears mixed with portions of lighter color.
Figure 3 illustrates the main characteristics observed for the mortars of the medieval walls of Gubbio. The OM direct observation was performed on disaggregated parts of the samples, while the polished section observation was performed on fragments of these same samples. This variation of the observed morphology is not, apparently, reflected in the results of the chemical analysis.
In general, the mortar contains coarse aggregate grains of calcareous lithotypes and, in some cases, the aggregates are in the range from 1 to 2 mm, angular to sub-rounded in shape. Fine aggregate grains consist of dominant limestone, polycrystralline sparite and chert and subordinate arenite, calcarenite, andmetamorphic and igneous rocks. Monocrystalline grains include quartz, plagioclase, K-feldspar, biotite, white mica, and sparry calcite. Foraminifera skeletons along with rare vegetable fibers and
cocciopesto fragments are also present. The binder is a poorly homogeneous micritic lime matrix with uncarbonated lumps of lime and ca. 5–10%vol porosity due to irregular-shaped voids and fissures (
Figure 4b). The internal cracks in the binder can have different causes, which may result from the process of hardening of the mortar, freezing and thawing cycles, mechanical movement processes, crystallization of salts, lack of adhesion between aggregates and binder, tensions caused by expansion and retraction of the components, and low quality of mortar preparation, among other factors [
18,
19].
From the elemental chemical analysis by wavelength dispersive X-ray fluorescence, samples of mortars from the Gubbio Town Walls show a higher amount of calcium and silica than other elements, which matches the results of other techniques and confirms that the mortar samples from the Gubbio Town Walls were lime mortars (
Table 2).
Despite the observations made by polarized light microscopy (PLM) of the assorted nature of the aggregate, X-ray diffraction results did not reflect this variety. The resulting data indicate that calcite and quartz are the main crystalline components for all samples, with very slight differences (
Figure 5). Other crystalline phases have been identified based on very low intensity peaks only in a few samples, being attributed to gypsum and possibly some feldspar. Gypsum was identified in samples presenting the highest sulphur content (
Table 2). It is important to note that XRD and WDXRF assays were performed in macerated samples, without the separation of the binder and aggregate. WDXRF results showed calcium and silicon as the components with the highest concentration for all samples. As observed by PLM, most of the aggregates, especially the coarser grains, are calcitic in nature, while the finer grains were identified as noncalcitic. Considering that the ligand is also composed of calcite, XRD results reflect the predominance in intensity of the crystalline phases of the main components.
Based on the results obtained, a relationship was established between the two main components identified, calcium and silicon (
Table 3) [
20,
21]. Although this relationship cannot correspond directly to a value of the ligand/aggregate ratio once calcium is included in components other than the ligand, as identified by polarized light microscopy (
Figure 4b), it may assist in the perception of a compositional trend between samples (
Figure 6). It is possible to perceive that the two samples that present Ca/Si ratio values close to or greater than 5 correspond to the samples collected in areas where the mortars were considered recent.
Despite the visible differences in the appearance of specimens observed in OM, the results obtained with TG-DTA showed a similar trend for all samples (
Figure 7), with calculated mass loss between 19% and 24%. Mass loss below 110 °C is not considered, because samples were kept in a drying oven for 1 h at that temperature before the start of the measurement for the elimination of the adsorbed water. For this study, the water loss of hydrated compounds was considered from the difference between the total mass loss and loss due to CO
2 during decarbonation. The main mass loss was observed in the endothermic peak starting at 600 °C associated with the release of CO
2, due to the process of decomposition of carbonates. The maximum processing temperature of the carbonate occurs between 750 °C and 850 °C [
6,
22]. In the case of the medieval wall samples, the maximum transformation takes place between 800 °C and 850 °C (
Figure 7).
Two of the samples present a DTA curve with a double endothermic peak near 130 °C, attributed to the loss of hydrated water from gypsum [
6,
23], which confirms the presence of this component in samples GTW4 and GTW9, also identified by XRD. This gypsum may be associated with the deterioration of the mortar, arising from the reaction with pollutants, or may have been added in the formulation of the mortar [
6]. The calculated values for mass loss and water loss resulting from TG analysis are presented in
Table 4. Water loss occurring below 200 °C corresponds to some water adsorbed and the loss of water from hydrated salts. Between 200 °C and 600 °C, that loss corresponds to the structural water of hydraulic compounds present in the samples [
6,
23,
24].
The degree of hydraulicity of a sample can be calculated by the ratio between the CO
2 loss above 600 °C and the water loss of the hydraulic compounds, occurring between 200 °C and 600 °C. The higher the value obtained by the CO
2/H
2O ratio, the lower the hydraulicity of the mortar is, being referenced that ratios greater than 10 are considered as typical lime mortars, values between 4 and 10 are hydraulic mortars, and values below 3 can be considered as pozzolan; sometimes, rations between 3.5 and 6 are considered as moderately hydraulic [
6,
9,
23].
Table 4 shows the CO
2/H
2O ratio calculated for the samples of the medieval walls. Only the GTW9 sample has a ratio greater than 10, which could be considered an aerial mortar. The other mortar samples can be considered as moderately hydraulic or with some hydraulic characteristic.