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Article

Petrographic and Chemical–Mineralogical Characterization of Mortars from the Cistern at Amaiur Castle (Navarre, Spain)

by
Graciela Ponce-Antón
1,*,
Maria Cruz Zuluaga
1,
Luis Angel Ortega
1 and
Juantxo Agirre Mauleon
2
1
Department of Mineralogy and Petrology, Faculty of Science and Technology, University of the Basque Country (UPV/EHU), Sarriena s/n, 48940 Leioa, Bizkaia, Spain
2
Aranzadi Society of Sciences, Zorroagagaina 11, 20014 Donostia-San Sebastián, Gipuzkoa, Spain
*
Author to whom correspondence should be addressed.
Minerals 2020, 10(4), 311; https://doi.org/10.3390/min10040311
Submission received: 11 March 2020 / Revised: 26 March 2020 / Accepted: 30 March 2020 / Published: 31 March 2020
(This article belongs to the Special Issue Mineralogy in Archaeometry and Cultural Heritage)
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Abstract

:
Mortars from the cistern in Amaiur Castle (Navarre, Spain) were analysed to assess the mortar manufacturing process and application techniques. To this end, optical microscopy, scanning electron microscopy (SEM), thermogravimetric analysis, X-ray fluorescence (XRF), X-ray diffraction (XRD), Raman microspectroscopy, and Fourier transform infrared spectroscopy (FTIR) were performed. The study of both structural and plaster mortars from Amaiur Castle cistern show patterns/rules in the mortar manufacture according to the specific construction requirements. A multilayer application technique was used for the construction of the cistern tank. Deliberate selection of the aggregate nature and grading contributed to mortar impermeability. Ceramic and silico-aluminous rock fragments were used as aggregates in the cistern tank to confer hydraulicity to the mortars, instead of carbonated aggregates as used in the vault. Aluminosilicated phases present in the aggregates led to the formation of amesite, which is a magnesium aluminosilicate hydrate (M-A-S-H) phase conferring hydraulicity to the mortar. Two types of additives were identified in the outer pigmented layer of plaster. Beeswax was the identified organic additive used to improve the impermeability of mortar, while hematite was the identified inorganic additive giving rise to the reddish colour of the layer.

1. Introduction

Cisterns have been essential structures for water storage since the Neolithic period not only to guarantee a regular and independent water supply in regions with water shortages but also to ensure the supply during drought or siege periods, particularly in castles or fortified sites [1,2,3,4]. The need to store and supply water required improvements in the hygienic conditions of the cisterns and led to structural and technological advances in the structures [5].
The great deteriorating capacity of water constitutes one of the main causes of construction material deterioration [6]. Cistern mortars are continuously in contact with water. Therefore, to ensure the impermeability and durability of mortars in the cistern tank, specific requirements are necessary compared with other building structures, in both the mortar manufacture and application technology practices [7].
Mortar impermeability is strictly related to mortar hydraulicity [8]. In hydraulic mortars, the hardening occurs mainly by the chemical reaction with water rather than by exposure to carbon dioxide as happens in non-hydraulic mortars. The amount of reactive silicates and aluminates present in the mixture will determine the hydraulicity degree of mortar [9]. To obtain the waterproofing of mortars, a reactive additive, mainly pozzolanic components such as crushed bricks or calcined clays, have been added to the mixture to provide hydraulic properties to non-hydraulic mortars, improving their resistance to moisture [10,11,12,13,14]. Pozzolans are highly reactive materials mainly composed of aluminosilicate phases that in the presence of water react with the calcium hydroxide [Ca(OH)2] and form stable aluminosilicate hydrated products that confer hydraulic properties to mortars [8,15]. Due to this reaction, a reaction rim can be formed surrounding the aggregates [16]. Moreover, natural organic compounds have also been added to the mixture to achieve specific behaviours in mortars [17].
The present study aims to perform petrographic and chemical–mineralogical characterisation of the structural and plaster mortars of the cistern from Amaiur Castle to assess the mortar manufacturing process and application technology used according to the specific requirements for the construction of this structure.

2. Geological and Archaeological Setting

Amaiur Castle (Navarre, Spain) is located geologically on Triassic limestones and dolostones, although Paleozoic and Mesozoic materials outcrop in the regional geology. The Paleozoic is characterized by Ordovician to Carboniferous metamorphic materials, consisting mainly of schist and quartzites and scarce limestones and dolomites, and by Permian carbonated and slaty breccias, limestones, and sandstones. Regionally, Triassic materials are characterised by conglomerates and sands in the Buntsandstein Facies, dolomitic limestones and dolostones in the Muschelkalk Facies, mottled clays with gypsum in the Keuper Facies, and subvolcanic basic rocks associated with the Keuper Facies [18,19].
The strategic emplacement of Amaiur Castle in the western Pyrenees allowed it to control the pass across this mountain range during the Middle Ages. Although the castle was first mentioned by written sources in the 12th century, the archaeological evidence showed an occupation period from the 13th century to the 17th century (Figure 1). Amaiur Castle defences were reinforced during the 14th century due to artillery development in that same century. Also in the 14th–15th century, a second wall reinforced the 13th–14th century medieval wall. During the 16th and 17th centuries, the castle was largely remodelled, owing to the conflicts occurring in the region at that time. In the 16th century, a circular bastion was added to the 14th–15th century medieval wall. The studied cistern was built at this time between the two medieval walls, giving rise to a rectangular-based tank cistern (Figure 2), and much of the space between the two medieval walls was filled with lime mortar. Later, in the 17th century, the fortification was transformed into a trace italienne bastion with the addition of diamond-shaped structures [20,21,22].

3. Materials and Methods

3.1. Materials

Seven representative lime mortar samples were collected from the preserved remains of the cistern (Table 1, Figure 1 and Figure 2). A total of six samples of structural mortar were collected, three from the walls of the tank (Samples CA-AL-7 and CA-AL-8 from the SE wall and Sample CA-AL-9 from the SW wall), two from the base of the barrel vault (Samples CA-AL-5 and CA-AL-6), and one from the vault lunette (CA-AL-2). Sample CA-AL-8 has been subdivided into two different samples (CA-AL-8a and CA-Al-8b) due to the granulometric differences observed on a macroscopic scale. Since both the tank walls and lunette are covered with the same plaster, an additional sample of plaster was collected from the lunette (CA-AL-1) in the area where the plastering is best preserved.

3.2. Methods

Petrographic characteristics of mortars were studied by polarized light microscopy (PLM) (JEOL, Tokyo, Japan) on polished thin sections and in both transmitted and reflected polarized light modes using a Nikon Eclipse LV100POL polarizing microscope equipped with a DS F-11 digital camera and DS L2 camera control unit.
Scanning electron microscopy (SEM) analysis was carried out on carbon-coated polished thin sections using a JEOL JSM-7000F Schottky-type field emission scanning electron microscope (JEOL, Tokyo, Japan) equipped with an INCA EDX detector X-sight Series Si (Li) Oxford pentaFET microanalysis system.
Thermogravimetric analysis (TGA) was performed using a TA SDT 2960 TG-DSC simultaneous instrument (TA Instruments, New Castle, DE, USA). A 5 to 7 mg of sample were heated in Pt crucibles at 2 °C min−1 from room temperature to 900 °C under a dry oxidizing atmosphere.
The semiquantitative chemical composition of major elements of the mortar binder fraction <2 µm was determined by means of X-ray fluorescence (XRF). A Wavelength Dispersive X-ray Fluorescence (WDXRF) PANalytical Axios Advanced PW4400 XRF spectrometer (with 4 kW Rh anode SST-mAX X-ray tubes) (Malvern PANalytical, Almelo, The Netherlands) was used to perform the analyses on a powder sample. The detection limit was of 0.01 wt%. The loss on ignition (LOI) was calculated after heating the powder sample at 900 °C.
The X-ray diffraction (XRD) analysis was performed to determine the mineralogy of powder polycrystalline samples using a Philips X’Pert diffractometer (Malvern PANalytical, Almelo, The Netherlands) equipped with a monochromatic Cu-ka1 X-radiation in a continuous scan from 5° to 70° 2θ operating at 40 kV and 20 mA conditions with an acquisition rate of 0.02° per second. X’Pert HighScore Plus 3.0 software by PANalytical (Malvern PANalytical, Almelo, The Netherlands) and the experimental patterns of the International Centre for Diffraction Data (ICDD) and the Inorganic Crystal Structure Database (ICSD) diffraction databases were used for the mineral phase identification.
Micro-Raman analyses were performed using a Renishaw inVia confocal microRaman spectrometer (Renishaw inVia, Gloucestershire, UK). Spectra were acquired between 1000 and 1120 cm−1 with a 1 cm resolution and the data acquisition was carried out using Renishaw’s WireTM 3.2 software package (Renishaw, Gloucestershire, UK). Raman spectra of pure standard compounds collected in the e-VISNICH dispersive Raman database were used to interpret the results.
Fourier transform infrared spectroscopy (FTIR) by the potassium bromide pellet technique was carried out to determine the nature of the organic compounds using a JASCO 4200 FTIR spectrometer (JASCO INTERNATIONAL CO., Hachioji, Tokyo, Japan) and acquiring spectra between 400 and 4000 cm−1.
To improve the FTIR signal of the organic components, an extraction was conducted using 200 µL of dichloromethane organic solvent.
Hydraulicity Index (HI) (Equation (1)) and Cementation Index (CI) (Equation (2)) values were calculated to assess the hydraulicity of the binder according to Boynton formula [24,25]. Indices were calculated as below:
HI = SiO 2 +   Al 2 O 3   CaO   +   MgO ,
CI = 2.8 SiO 2 + 1.1 Al 2 O 3 + 0.7 Fe 2 O 3 CaO   + 1.4 MgO .

4. Results

4.1. Petrographic and Chemical–Mineralogical Characterization

Macroscopically, a difference in the nature of aggregates was observed between the plaster (Figure 3a), mortars from the tank (Figure 3b–d), and the mortars from the vault (Figure 3e,f). Sample CA-AL-2 from the lunette of the vault and Samples CA-AL-5 and CA-AL-6 from the base of the barrel vault (structural mortars) show carbonated aggregates, whereas Samples CA-AL-7, CA-AL-8 and CA-AL-9 (structural mortars), and Sample CA-AL-1 (plaster) show siliceous aggregates. Mortars from the tank also show increasing aggregate grading, from structural mortars (inner part; Samples CA-AL-7, CA-AL-8, and CA-AL-9) to the plaster (outer part; Sample CA-AL-1) (Figure 3).
Microscopically, all samples show a heterogeneous binder matrix-supported texture with aggregates embedded in a micritic calcite matrix. Petrographic observations of mortar identified the carbonated aggregates of samples from the vault as poorly sorted fine-grained dolostone fragments with angular to subangular shape (Figure 4a). The grain sizes of aggregates from the vault base (Samples CA-AL-5 and CA-AL-6) range from 0.2 mm up to 3 mm, whereas aggregates from the lunette (CA-AL-2) reach 8 mm in size. Dolostone aggregates show a pronounced reaction zone (Figure 4a). Scarce ceramic fragments can also be observed dispersed in the binder matrix.
The nature of the aggregates from the cistern tank mortars is the same in both structural mortars (Samples CA-AL-7, CA-AL-8, and CA-AL-9) and plaster (Samples CA-AL-1). Mortars are mainly composed of subangular to rounded ceramic fragments (s.l.), and the siliceous aggregates observed macroscopically have been identified as well-rounded quartz grains and phyllite, schist, quartzite, sandstone, and subvolcanic rocks (Figure 4b–e). Dolostone fragments were also observed in minor amounts, and also some charcoal fragments were dispersed in the binder matrix. Heterometric lime lumps up to 4 mm were also observed (Figure 4e).
The grain size of aggregates decreases and aggregate sorting increases from the inner layer of the structural mortar (Sample CA-AL-7) to the outer part (CA-AL-8 and CA-AL-9). Sample CA-AL-7 shows very poorly sorted aggregates from 0.7 mm to 2 cm in size. The outer part of Sample CA-AL-8 (CA-AL-8a) is very similar to Sample CA-AL-9, with smaller and more sorted aggregates than the inner part of Sample CA-AL-8 (CA-AL-8b). Both Subsample CA-AL-8b and Sample CA-AL-9 show moderately sorted aggregates ranging from 0.2 mm up to 3 mm in grain size, whereas Subsample CA-AL-8a shows better sorted aggregates from 0.1 to 1.3 mm in size.
Sample CA-AL-1 corresponding to the plaster mortar consists of two different layers (Figure 4f). The inner layer of the plaster is also composed by the well-rounded and sorted ceramic and polygenic rock aggregates, as observed in the structural mortars of the cistern, which are up to 0.3 mm in size. The outer layer of the plaster is a reddish pigmented layer around 0.15 mm thick showing a scarce amount of mica-like phyllosilicates and quartz grains.
Binder/aggregate ratios were defined by the comparison of the chart for volume percentage estimation [26]. Samples show a binder/aggregate ratio between 1:2 and 1:1, except for Sample CA-AL-7, which shows a binder/aggregate ratio of 1:1 and the inner layer of plaster, which shows a binder/aggregates ratio of 2:1.
To determine the composition of the mortar binders, Sample CA-AL-2 from the vault lunette, Sample CA-AL-9 from the structural mortars of the tank, and both inner and pigmented layers of plaster (Sample CA-AL-1) were selected for X-ray diffraction (XRD) analysis.
A binder fraction <2 µm of Samples CA-AL-2 and CA-AL-9 was extracted in order to avoid the interference of the aggregate composition following the procedures described by Ortega et al. [27] and Ponce-Anton et al. [28]. The small amount of Sample CA-AL-1 from the plaster made it impossible to extract the binder fraction <2 µm, and thus the bulk fraction of both inner and pigmented layers was analysed. For the analysis of the inner layer, the aggregates observable with the naked eye were removed.
The XRD results are shown in Figure 5. All samples are mainly composed of magnesium calcite [(Ca, Mg)CO3], and in minor amounts, hydrotalcite [Mg6Al2(CO3)(OH)16·4(H2O)] was also detected in all samples, except in the pigmented layer where only traces were detected. Quartz [SiO2] and illite-like phyllosilicates were detected in samples from the cistern tank in both structural and plaster mortars. Reflection peaks at 7.03 Å and 3.51 Å allowed to detect small amounts of the amesite mineral phase [Mg2Al2SiO5(OH)4] in Sample CA-AL-9 and in the inner layer of the plaster. Hematite [Fe2O3] was also identified in the pigmented outermost layer of the plaster.
Both hydrotalcite and amesite have been the Mg-hydrated phases detected by XRD. Hydrotalcite is a layered double hydroxide phase (LDHs) [29], whereas amesite is a magnesium aluminosilicate hydrate phase (M-A-S-H).
To confirm the presence of the Mg-hydrated phases detected by XRD, the binder fraction <2 µm of Samples CA-AL-2 (vault mortar) and CA-AL-9 (tank mortar) were analysed by thermogravimetric analysis (TGA). The TGA results are shown in Figure 6.
Sample CA-AL-2 shows a total weight loss of 38.14%, whereas Sample CA-AL-9 shows a total weight loss of 28.17%. Since the total weight loss of pure calcium carbonate is 44%, these lower weight losses indicate the presence of other mineral phases in the binder as indicated by the XRD results (Figure 5).
The TGA curves show four main weight loss regions. The first weight loss (<120 °C) and the second weight loss (120 to 200 °C) are attributed to the adsorption water and poorly bonded interlayer water, respectively. The third weight loss (200 to 600 °C) is attributed to dehydration caused by the loss of hydroxyl groups (OH−). The last fourth weight loss (600 to 800 °C) is related to the decomposition of the carbonates [30,31,32]. No weight loss is observed over 800 °C. Considering the DSC curve, between 200 and 600 °C, two endothermic peaks are observed in both Sample CA-AL-2 and Sample CA-AL-9. These two endothermic peaks correspond to the hydrotalcite (LDHs), which decomposes in two steps in this range of temperatures [33,34]. Nevertheless, the second endothermic peak between 450 and 600 °C can also be related to the decomposition of the amesite (M-A-S-H) and illite-like phyllosilicates [35,36,37,38] present in Sample CA-AL-9, and therefore, they appear to overlap. Between 800 and 900 °C, an endothermic peak is only detected in Sample CA-AL-9, confirming the presence of amesite and illite in the tank mortar sample, since the breakdown of both phases takes place in this temperature range [35,36,37].
X-ray fluorescence was performed to determine the chemical composition of the binder fraction <2 µm of Samples CA-AL-2 and CA-AL-9. Chemical results of both vault and tank mortars (Samples CA-AL-2 and CA-AL-9, respectively) were used to calculate the Hydraulicity Index (HI) and Cementation Index (CI) in order to assess and compare the hydraulicity degree of binders from the vault and tank (Table 2). Hydraulicity is classified as weak (HI = 0.1–0.2, CI = 0.3–0.5), moderate (HI = 0.2–0.4, CI = 0.5–0.7), and eminent (HI < 0.4, CI = 0.7–1.1) [24,25]. According to the HI and CI values, the mortar binder from the cistern tank is eminently hydraulic, whereas the mortar binder from the vault is weakly hydraulic.

4.2. Study of the Pigmented Layer of Plaster

Scanning electron microscopy (SEM) was performed on Sample CA-AL-1 for better characterization of the plaster. SEM observations show that the pigmented layer of plaster is less porous than the inner layer and that the contact surface between both layers is rough (Figure 7).
The outermost pigmented layer of the plaster was also analysed by Raman spectroscopy and Fourier transform infrared spectroscopy (FTIR) in order to determine whether any other type of additive was used in the manufacture. Raman spectroscopy confirmed that the pigmented layer of plaster is mainly composed of a mixture of calcite and hematite (Figure 8a).
Raman spectra show intense bands at 282 cm−1, 712 cm−1, and 1087 cm−1 attributed to calcite and less intense bands at 226 cm−1, 294 cm−1, and 410 cm−1 attributed to hematite [39,40]. Broad bands at 355 and 464 cm−1 related to quartz are also observed. The broad band identified in the region of 1150–1450 cm−1 is attributed to an organic compound, but due to the low quality of the spectrum, it was difficult to identify (Figure 8b).
Infrared spectroscopy (FTIR) analysis was performed in order to identify the organic compound detected by Raman spectroscopy. FTIR spectra show bands at 2864 cm−1, 2514 cm−1, 1794 cm−1, 1428 cm−1, 871 cm−1, and 711 cm−1 attributed to calcite and bands at 1027 cm−1, 642 cm−1 and 528 cm−1 attributed to the hematite (red earth pigment) (Figure 9a) [41,42,43]. Nevertheless, the strong absorption of the inorganic phases hides the signal of the organic compound, hindering its identification. To improve the FTIR signal of the organic component, an extraction was conducted using 200 µL of dichloromethane. The resulted supernatant was evaporated on a potassium bromide disk to be then analysed. The intense bands detected at 2955 cm−1, 2916 cm−1, 2848 cm−1, 1736 cm−1, and 1472 cm−1 were attributed to beeswax organic compound (Figure 9b) [43].

5. Discussion

Petrological study suggests a careful process in both the mortar manufacture and mortar application technique for the cistern construction according to the specific characteristics needed for this structure. The impermeability of the cistern tank is an essential requirement for appropriate water storage. Mortar impermeability is strictly related to mortar hydraulicity, which is favoured by the use of silico-aluminous aggregates working as reactive materials in the mixture [8,10,11,12,13]. The use of silico-aluminous rocks and ceramic fragments as aggregates in the tank mortar manufacture, instead of the carbonated aggregates used for the vault mortars, indicates a deliberate selection of aggregates in order to confer hydraulicity to the mortar to obtain waterproof mortars. Furthermore, the use of silico-aluminous aggregates adds greater cohesion and mechanical strength to the mortar [44,45].
The raw materials that were used as aggregates to manufacture both the lime mortars from the vault and cistern tank correspond to the surrounding geological materials. Not only the selection of aggregates was important but also the aggregate sorting. The grain size of aggregates in the tank mortars becomes smaller and better sorted from the first layer of the structural mortar toward the outermost pigmented layer of the plaster. Besides, aggregate size also contributes to material reactivity, since the smaller the size, the higher the specific surface area and thus the higher the reaction rate [8,46,47,48]. Furthermore, mortar porosity is lower in mortars with better-sorted aggregates since they produce a better-packed system [49,50,51,52].
The mineralogical analyses allowed identifying additives in the pigmented layer. The XRD, Raman, and FTIR analyses indicate that hematite was used as an inorganic additive, which led to the reddish colour of the pigmented layer (Figure 5, Figure 8 and Figure 9). Hematite would not be related to ceramic fragments, since they were not observed either in the petrographic study or by XRD (Figure 4f and Figure 5d). Therefore, the hematite may have been deliberately added. FTIR analyses allowed identifying the beeswax as the organic additive in the pigmented layer (Figure 9). Beeswax was the most common natural wax used as an organic additive to provide impermeability and sealing property to the materials [53]. Since organic compounds are more susceptible to degradation than inorganic compounds, knowledge of the composition of ancient additives is essential for appropriate interventions on archaeological structures [53,54].
Therefore, to ensure the impermeability of the cistern tank, a multilayer application of different mortars was performed using silico-aluminous aggregates and decreasing their grain size from the first layer of the structural mortar toward the inner layer and applying a final plaster with a beeswax-bearing pigmented layer (Figure 10).
Furthermore, the reaction zones observed in dolomitic aggregates resulted from the dedolomitization of dolomitic aggregates, and the presence of hydrotalcite in the binder has been related to the use of the traditional hot-mixing method in mortar manufacture [23]. In the manufacture of cistern tank mortars, the use of this traditional hot-mixing method would also be expected since reaction zones were not only observed at the edge of the dolomitic aggregates, but they also stand out in the ceramic fragments and some silico-aluminous aggregates (Figure 4a–d).
Quartz and phyllosilicates are attributed to the ceramic fragments and silico-aluminous rocks used as aggregates, whereas magnesium calcite, hydrotalcite, and amesite are mineral phases formed during mortar manufacture (Figure 5). Magnesium calcite is formed in the setting of mortar as a result of the lime cycle [24,55], and hydrotalcite is a carbonated mineral formed during the slaking process in the presence of available magnesium content [28].
Hydrotalcite has been identified in all analysed mortar binders (Figure 5). Magnesium released from the dedolomitization process, leading to the formation of the reaction zone in the edge of dolomitic aggregates, and the aluminium released from the breakdown of phyllosilicates favours the formation of hydrotalcite [23,56,57,58]. Nevertheless, some amount of magnesium and aluminium can also come from the lime used for the mortar manufacture when impure limestones or partially dolomitized limestones have been used as the raw material for lime production [28,59]. Therefore, the presence of hydrotalcite and the absence of dolomitic aggregates in the pigmented layer of plaster (Figure 4 and Figure 5) would indicate the use of impure limestones or partially dolomitized limestones for the production of lime for the cistern construction.
The aluminosilicate phases present in the silico-aluminous aggregates of the tank mortars are highly reactive materials that in the presence of alkalis react with water, forming a wide family of hydration products that induce hydraulic properties to the mortars [8,15,46]. Reaction zones observed in the edge of the silico-aluminous aggregates suggest the development of this reaction (Figure 4b–d). The reaction between aluminosilicate phases and an alkaline solution is known as an alkali-silicate reaction (ASSR), which is a specific type of alkali-silica reaction (ASR) [60,61,62].
Amesite has been the only aluminosilicate hydrated phase detected in the tank mortars. This mineral phase has also been described in some mortars with pozzolanic aggregates [48,63]. Amesite is a magnesium aluminosilicate hydrate (M-A-S-H) phase, and although it is chemically related to chlorites, it displays a similar structure to serpentine with alternating tetrahedral and trioctahedral layers [37]. The amesite has only been detected in samples containing silico-aluminous aggregates, indicating that it would have formed as a result of the reaction between the aluminosilicate phases and the putty alkalis.
Magnesium silicate hydrate (M-S-H) phases have been described during the hydration of MgO-bearing lime materials and formed by the reaction between magnesium and silicate ions [64,65,66]. The M-S-H phases show a layered structure and have been related to poorly crystalline phyllosilicates [64,66,67,68,69]. The reaction zone of the dolomitic aggregates of the structural mortars from Amaiur Castle showed the presence of M-S-H phases, which are suggested as a result of an ASSR, although the presence of the M-S-H phases could not be confirmed [23]. According to Mackenzie and Bowden [37], amesite is formed by the substitution of the Si4+ in the tetrahedral layers and the Mg2+ in the octahedral layers by the Al3+. Therefore, the amesite detected in the mortars from the cistern tank could also have been formed as a result of the ASSR, since the kinetic formation of M-A-S-H phases has been described as similar to M-S-H phases, incorporating aluminium into the structure [63,70].
Besides, the phases formed as a result of the reaction between the aluminosilicate phases of the silico-aluminous aggregates and the putty alkalis contribute to decreasing the porosity and therefore favour the waterproofing of the cistern tank [45,71,72,73].
The study of both structural and plaster mortars from Amaiur Castle cistern show patterns/rules in the mortar manufacture according to the specific construction requirements, distinguishing two kinds of mortars with aggregates of different nature. Mortars from the cistern tank acquired hydraulicity by the addition of silico-aluminous rocks and ceramic fragments as aggregates.

6. Conclusions

The study of the mortars from the Amaiur Castle cistern has allowed assessing the knowledge of the mortar manufacturing process and the mortar application techniques to ensure the structure waterproofing necessary for the correct storage of water.
The cistern shows three types of lime mortars with different compositional characteristics related to the specific function within the structure: structural mortars from the barrel vault, structural mortars from the tank, and plaster.
The nature of the aggregates used in the manufacture of cistern mortars was different, according to specific construction requirements. Carbonated aggregates were used in the vault mortar and silicious and silico-aluminous aggregates in the tank mortars and plaster, suggesting the specific selection of raw materials.
The raw materials of the surrounding geological materials were used for the manufacture of the lime mortars of the cistern of the Amaiur Castle.
To confer hydraulicity to the mortars of the cistern tank and achieve the waterproofing of the structure, ceramic fragments and silico-aluminous rocks were used as aggregates in the manufacture.
Besides, the reaction zones on the edge of silico-aluminous rocks and ceramic aggregates resulted from an alkali silicate reaction (ASSR) that favoured the formation of amesite, the magnesium aluminosilicate hydrated (M-A-S-H) phase detected in the binder of the tank mortars.
A multilayering application technique was performed in the construction of the cistern tank. Two/three layers have been differentiated in the structural mortar from the tank, with a decrease in grain size and an improvement in sorting of aggregates from the inner part to the outer part. The plaster is formed by two layers: an inner layer and an outer pigmented layer.
The pigmented layer of plaster is composed by two types of additives. Hematite was identified as an inorganic additive giving rise to the reddish colour of the layer. Additionally, beeswax was identified as an organic additive used to confer impermeability to the pigmented layer.
The presence of hydrotalcite and the absence of dolomitic aggregates in the pigmented layer point to the use of impure limestones or partially dolomitized limestones as the raw material for the production of lime at Amaiur Castle.

Author Contributions

Conceptualization, G.P.-A., M.C.Z. and L.A.O.; Data Curation, G.P.-A. and M.C.Z.; Writing—Original Draft Preparation, G.P.-A.; Writing—Review and Editing, G.P.-A., M.C.Z.; Funding Acquisition, L.A.O. and J.A.M. All authors have read and agreed to the published version of the manuscript.

Funding

This research was funded by the IT1193-13 project of the Basque Government.

Acknowledgments

G.P.-A. acknowledges the PhD research grant of the Basque Government 2015-1-02-35. The authors would like to thank Peter Smith for reviewing the use of English in the manuscript.

Conflicts of Interest

The authors declare no conflict of interest.

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Figure 1. Geographic location of Amaiur Castle (Navarre, Spain). Studied samples are marked by red circles. Modified from Ponce-Antón et al. [23].
Figure 1. Geographic location of Amaiur Castle (Navarre, Spain). Studied samples are marked by red circles. Modified from Ponce-Antón et al. [23].
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Figure 2. Location of the studied samples within the cistern. Cistern tank in green, vault lunette in blue, barrel vault in yellow, and 14th–15th centuries wall in black.
Figure 2. Location of the studied samples within the cistern. Cistern tank in green, vault lunette in blue, barrel vault in yellow, and 14th–15th centuries wall in black.
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Figure 3. Macroscopic texture of the lime mortars from the Amaiur Castle cistern. (a) CA-AL-2, plaster sample. (b) CA-AL-8a, (c) CA-AL-8b, and (d) CA-AL-7, samples from the tank mortars. (e) CA-AL-2 and (f) CA-AL-5, mortars from the vault. Mortars from the tank show an increase in aggregate grading from the inner part (d) to the outer part (a).
Figure 3. Macroscopic texture of the lime mortars from the Amaiur Castle cistern. (a) CA-AL-2, plaster sample. (b) CA-AL-8a, (c) CA-AL-8b, and (d) CA-AL-7, samples from the tank mortars. (e) CA-AL-2 and (f) CA-AL-5, mortars from the vault. Mortars from the tank show an increase in aggregate grading from the inner part (d) to the outer part (a).
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Figure 4. Photomicrographs showing the most representative microtextures of the lime mortars from Amaiur Castle cistern. (a), (b)-left, (c) and (d)-left: plane polarized light mode (PPL). (b)-right, (d)-right, (e,f): crossed-polarized light mode (XPL). C: ceramic; DRx: dolostone; L: lime lump; PhRx: phyllite; PL: pigmented layer; QRx: quartzite; Qz: quartz; R: reaction zone; ScRx: Schist; SvRx: subvolcanic rock.
Figure 4. Photomicrographs showing the most representative microtextures of the lime mortars from Amaiur Castle cistern. (a), (b)-left, (c) and (d)-left: plane polarized light mode (PPL). (b)-right, (d)-right, (e,f): crossed-polarized light mode (XPL). C: ceramic; DRx: dolostone; L: lime lump; PhRx: phyllite; PL: pigmented layer; QRx: quartzite; Qz: quartz; R: reaction zone; ScRx: Schist; SvRx: subvolcanic rock.
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Figure 5. X-ray diffraction patterns of the lime mortars from Amaiur Castle cistern. (a) Binder fraction <2 µm from the lunette. (b) Binder fraction <2 µm from the structural mortar of the tank. (c) Bulk fraction from the inner layer of the plaster mortar. (d) Bulk fraction from the pigmented layer of the plaster mortar. Ame: amesite, Hem: hematite, HT: hydrotalcite; Mg-cal: magnesium calcite, Phy: phyllosilicates s.l., Qz: quartz.
Figure 5. X-ray diffraction patterns of the lime mortars from Amaiur Castle cistern. (a) Binder fraction <2 µm from the lunette. (b) Binder fraction <2 µm from the structural mortar of the tank. (c) Bulk fraction from the inner layer of the plaster mortar. (d) Bulk fraction from the pigmented layer of the plaster mortar. Ame: amesite, Hem: hematite, HT: hydrotalcite; Mg-cal: magnesium calcite, Phy: phyllosilicates s.l., Qz: quartz.
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Figure 6. Thermogravimetric analyses of the binder fraction <2 µm from the vault mortar (Sample CA-AL-2 in black) and tank mortar (Sample CA-AL-9 in green).
Figure 6. Thermogravimetric analyses of the binder fraction <2 µm from the vault mortar (Sample CA-AL-2 in black) and tank mortar (Sample CA-AL-9 in green).
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Figure 7. SEM image of the cistern plaster. A: pigmented layer; B: inner layer. Rough contact surface in red.
Figure 7. SEM image of the cistern plaster. A: pigmented layer; B: inner layer. Rough contact surface in red.
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Figure 8. Raman spectroscopy of the bulk fraction of the pigmented layer of the cistern plaster. (a) Raman spectra showing the highest intensities bands of calcite, hematite, and quartz. (b) Raman spectra showing an organic compound in the region of 1150–1450 cm−1. Calcite bands at 282 cm−1, 712 cm−1, and 1087 cm−1; hematite bands at 226 cm−1, 294 cm−1, and 410 cm−1; quartz bands at 355 cm−1 and 464 cm−1.
Figure 8. Raman spectroscopy of the bulk fraction of the pigmented layer of the cistern plaster. (a) Raman spectra showing the highest intensities bands of calcite, hematite, and quartz. (b) Raman spectra showing an organic compound in the region of 1150–1450 cm−1. Calcite bands at 282 cm−1, 712 cm−1, and 1087 cm−1; hematite bands at 226 cm−1, 294 cm−1, and 410 cm−1; quartz bands at 355 cm−1 and 464 cm−1.
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Figure 9. Fourier transform infrared spectroscopy (FTIR) analysis of the pigmented layer of the cistern plaster. (a) FTIR spectra showing the highest intensities bands of calcite and hematite (red earth). (b) FTIR spectra showing the highest intensities bands of the organic compound identified as beeswax. Calcite bands at 2864 cm−1, 2514 cm−1, 1794 cm−1, 1428 cm−1, 871 cm−1, and 711 cm−1; hematite (red earth) bands at 1027 cm−1, 642 cm−1, and 528 cm−1. Beeswax bands at 2955 cm−1, 2916 cm−1, 2848 cm−1, 1736 cm−1, and 1472 cm−1.
Figure 9. Fourier transform infrared spectroscopy (FTIR) analysis of the pigmented layer of the cistern plaster. (a) FTIR spectra showing the highest intensities bands of calcite and hematite (red earth). (b) FTIR spectra showing the highest intensities bands of the organic compound identified as beeswax. Calcite bands at 2864 cm−1, 2514 cm−1, 1794 cm−1, 1428 cm−1, 871 cm−1, and 711 cm−1; hematite (red earth) bands at 1027 cm−1, 642 cm−1, and 528 cm−1. Beeswax bands at 2955 cm−1, 2916 cm−1, 2848 cm−1, 1736 cm−1, and 1472 cm−1.
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Figure 10. Schematic image of the multilayer application technique for mortars in Amaiur Castle cistern. The cistern tank is shown in green, the vault lunette is shown in blue, the barrel vault is shown in yellow, and the 14th–15th centuries wall is shown in black.
Figure 10. Schematic image of the multilayer application technique for mortars in Amaiur Castle cistern. The cistern tank is shown in green, the vault lunette is shown in blue, the barrel vault is shown in yellow, and the 14th–15th centuries wall is shown in black.
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Table
Table 1. Lime mortar samples from the different locations in Amaiur Castle cistern.
Table 1. Lime mortar samples from the different locations in Amaiur Castle cistern.
Mortar TypeStructureLocationSample
Structural Barrel vaultLunetteCA-AL-2
BaseCA-AL-5
CA-AL-6
TankInner layerCA-AL-7
Outer layerCA-AL-8CA-AL-8b
CA-AL-8a
CA-AL-9
PlasterInner layerCA-AL-1
Pigmented layer
Table
Table 2. Semiquantitative results of the major elements of the binder fraction <2 µm in powder samples from the lunette of the barrel vault and tank samples determined by X-ray fluorescence, the hydraulicity index (HI), and the cementation index (CI). Chemical results are expressed as oxides in wt%. Iron content is expressed as total Fe2O3t. LOI: loss on ignition (%).
Table 2. Semiquantitative results of the major elements of the binder fraction <2 µm in powder samples from the lunette of the barrel vault and tank samples determined by X-ray fluorescence, the hydraulicity index (HI), and the cementation index (CI). Chemical results are expressed as oxides in wt%. Iron content is expressed as total Fe2O3t. LOI: loss on ignition (%).
SampleStructureMgOAl2O3SiO2K2OCaOTiO2MnOFe2O3tLOIHICI
CA-AL-2Lunette6.162.435.550.2344.730.200.052.4038.140.200.37
CA-AL-9Tank6.708.1521.121.0829.200.350.154.8828.170.951.85

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Ponce-Antón, G.; Zuluaga, M.C.; Ortega, L.A.; Agirre Mauleon, J. Petrographic and Chemical–Mineralogical Characterization of Mortars from the Cistern at Amaiur Castle (Navarre, Spain). Minerals 2020, 10, 311. https://doi.org/10.3390/min10040311

AMA Style

Ponce-Antón G, Zuluaga MC, Ortega LA, Agirre Mauleon J. Petrographic and Chemical–Mineralogical Characterization of Mortars from the Cistern at Amaiur Castle (Navarre, Spain). Minerals. 2020; 10(4):311. https://doi.org/10.3390/min10040311

Chicago/Turabian Style

Ponce-Antón, Graciela, Maria Cruz Zuluaga, Luis Angel Ortega, and Juantxo Agirre Mauleon. 2020. "Petrographic and Chemical–Mineralogical Characterization of Mortars from the Cistern at Amaiur Castle (Navarre, Spain)" Minerals 10, no. 4: 311. https://doi.org/10.3390/min10040311

APA Style

Ponce-Antón, G., Zuluaga, M. C., Ortega, L. A., & Agirre Mauleon, J. (2020). Petrographic and Chemical–Mineralogical Characterization of Mortars from the Cistern at Amaiur Castle (Navarre, Spain). Minerals, 10(4), 311. https://doi.org/10.3390/min10040311

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