The thermal decomposition of a kaolinite:dimethyl sulfoxide intercalate has been studied by thermogravimetry. The decomposition is complete by 175°C and has a ΔH of 58 ± 5 kJ/mole of dimethyl sulfoxide. For the first 70–80% of the reaction a plot of log(l — α) vs. time is linear, where α is the reaction fraction complete. A two-dimensional, contracting-circle type of mechanism is consistent with this linearity, provided that the nucleation process is considered to be exponential rather than instantaneous. An activation energy of 105 ± 8 kJ/mole of dimethyl sulfoxide has been derived. This value is inconsistent with the simple assumption that the rate-determining step is the freeing of single organic molecules from their bonding to the clay layers. The mechanism of this decomposition is different from that found for kaolinite: N-methyl formamide, and the activation energy is considerably greater than that found for that material (30 ± 3 kJ/mole).

To explain the large values of the quadrupole splittings and line widths in the Mössbauer spectrum of oxybiotite, a formalized analysis of the distribution of effective charges in the anion network was conducted using an idealized model of the biotite octahedral layer. Based on this analysis, a qualitative physical model has been proposed, according to which the Mössbauer spectrum consists of a superposition of six quadrupole doublets. The proposed model explains the appearance of residual magnetization well below the biotite decomposition temperature. Annealing the biotite at 1070°K leads to the formation of nuclei of the magnetic phase in chains consisting of R3+ and vacancies. This phase is the decomposition product of biotite at 1370°K, i.e., a ferrispinel having Fe2−xMgAlxO4 (x = 0.5–0.6) composition.

The thermal decomposition behavior of hydrotalcite-like compounds (HTlcs) prepared by reconstruction of calcined HTlcs is described. From the results of X-ray diffraction (XRD), it seems that dicarboxylate intercalates of HTlc calcined at 500 °C are completely reconstructed to Mg-Al-CO3 HTlc by exposure to aqueous Na2CO3. However, the Mg-Al-CO3 HTlc reconstructed under particular conditions yields spinel (MgAl2O4) at 400 °C. This temperature is very low, because Mg-Al-CO3 HTlc that has been reported yields spinel at 900 °C after forming a Mg-Al double oxide. The reconstructed Mg-Al-CO3 HTlc that yields spinel at 400 °C is obtained when the following conditions are fulfilled: the crystallites of the starting dicarboxylate intercalates are coagulated tightly and the calcined HTlcs and reconstructed materials are not ground. The Mg-Al-CO3 HTlc reconstructed under these conditions contains only 55–70% of carbonate anions required by stoichiometry. Therefore, we conclude that the transformation of reconstructed Mg-Al-CO3 HTlc to spinel at 400 °C is the result of a reaction occurring between edges of crystallites.

The absolute dating of mortar by accelerator mass spectrometry (AMS) has been the subject of renewed interest for several years. International intercomparison campaigns, called MODIS (MOrtar Dating Intercomparison Study), have been carried out. The first MODIS-1 campaign highlighted limitations in mortar dating, due to the similarity between the primary material to be dated (binder) and the contaminant (exogenous CaCO3). Methods have since emerged to overcome this problem and the need for a good preliminary characterization has been proven. The Laboratoire de Mesure du Carbone 14 (LMC14) took part in the second intercomparison campaign, MODIS2, by applying thermal decomposition increments to distinguish the carbonated binder, the organic matter contaminants (late in formation pyrogenic carbonate, LDH) and limestone. The LMC14 results on MODIS2 are quite conclusive on “pure” re-carbonated lime mortar binders containing little contaminant geological limestone but show their weaknesses for mortars heavily contaminated in Dolomites, which are difficult to discern from the binder. Recommendations for users of radiocarbon (14C) dating on mortar-based materials are made in the conclusion.

Different changes in the structural and thermal properties of various types of talc have been reported in the literature which have made comparison of analytical results difficult. The objective of the present study was to obtain some fundamental insights into the effects of the thermal behavior of talc and to carry out kinetic analyses of the decomposition of talc under high temperature. X-ray diffraction (XRD), Fourier-transform infrared spectroscopy (FTIR), and thermogravimetry-differential scanning calorimetry (TG-DSC) were used to study the thermal decomposition mechanism. The Coats-Redfern decomposition model was used to determine the decomposition mechanism of talc samples. The results showed that the decomposition of talc commenced at ~800°C, peaking at ~895°C, with the formation of enstatite and amorphous silica. An isothermal treatment at 1000°C caused the complete dehydroxylation of talc. The XRD and FTIR results indicated that the enstatite and amorphous silica phases were transformed into clinoenstatite and paracrystalline opal phases, respectively, after the decomposition stage at 1200°C. Good linearity in the Coats-Redfern model was observed from room temperature to 1300°C and the activation energy was calculated to be 69 kcal/mol.

The preparation and characterization of intercalated kaolinite is important for industries such as those using nanocomposites, but the number of compounds that can be intercalated into these clay minerals is rather limited. The purpose of this study was to expand the range of possible intercalants by developing intercalation precursors using both single and multiple (co-intercalation) precursor agents. Characterization of the resulting precursors was by X-ray powder diffraction (XRD), Fourier transform infrared spectroscopy (FTIR), thermogravimetric analysis (TGA), and differential thermal analysis (DTA). The results show that the most successful single intercalation agent was DMSO and, among the co-intercalation agents, the DMSO/CH3OH system was the best. The preparation and characterization of kao-DMSO-KAc showed that the displacement reaction is the most efficient way to expand the interlayer spacing of kaolinite. At the same time, the lateral-bilayer arrangement of the Ac− in the interlayers was proven by study of de-intercalation of kao-KAc under high temperature.

The search for signs of life is a major objective in the exploration of Mars. Of particular interest are chemical biosignatures such as biomolecules. However, molecular biosignatures are susceptible to extreme environmental conditions such as heat, ionising radiation and strong oxidants. Therefore, a knowledge of the stability of possible biosignature molecules under present and past conditions on Mars is important, as well as the nature of possible alteration products. In the light of the long volcanically active history of Mars, we have studied the thermal behaviour of selected biological compounds, namely, haemin (an iron porphyrin closely related to the haem prosthetic group), cytochrome c (a small protein) and lecithin (a mixture of phospholipids). Samples were exposed to temperatures up to 900°C under an inert atmosphere of nitrogen, either in neat form or in mineral matrices. The matrix materials used were sodium chloride, gypsum (CaSO4 ⋅ 2H2O), Ca-montmorillonite (STx-1b), the Martian regolith simulant JSC Mars-1A and some mixtures thereof. Key results are: (1) The onset of significant decomposition for haemin, cytochrome c and lecithin occurs around 240°C. At slightly higher temperatures the disappearance of all characteristic infrared spectral bands indicates complete decomposition and loss of the primary biosignatures. (2) Haemin stoichiometrically releases CO2 and HCl during the initial thermal decomposition phase, at the end of which the iron porphyrin core is still intact. High-temperature products of haemin include graphite, α-iron and cementite (Fe3C). (3) Neat lecithin forms long-chain polyphosphates at 500°C, whereas lecithin‒NaCl mixtures form diphosphate (pyrophosphate). As these anions are absent and rare, respectively, in minerals, they may potentially serve as secondary biosignatures. (4) Heating a mixture of NaCl and JSC Mars-1A at 800°C in the presence of lecithin produces the aluminosilicate mineral sodalite (Na8[AlSiO4]6Cl2), which however appears to be of limited use as a secondary biosignature.

Dating lime mortar samples using the radiocarbon (14C) method can be difficult. This is because the contamination is similar to the primary dating material (CaCO3) and consequently difficult to remove. Mortar can also have late-in-formation pyrogenic carbonate from interactions with the environment after the initial hardening phase, such as recrystallization, fire damage or delayed hardening. When 14C dating a system of primary dating material, contamination and late-in-formation pyrogenic carbonate, one approach is multi-fraction dating with conclusiveness criteria. If a sample has sufficient contamination or late-in-formation pyrogenic carbonate, the criteria evaluate the result inconclusive. To improve inconclusive results from such samples, this study investigates sample preparation by thermal decomposition. Here samples that were inconclusively dated by the authors’ traditional method, sequential dissolution with 85% phosphoric acid, are investigated further. This study finds that CO2 thermally decomposed at low temperatures contains some late-in-formation pyrogenic carbonate. By rejecting CO2 decomposed at low temperatures, Kastelholm castle and Kimito church in Finland are conclusively and accurately dated. Furthermore, a preheating method removes some late-in-formation carbonate, but not enough for a conclusive result. Finally, thermal decomposition finds difficulty in discerning binder carbonate from limestone and marble contamination.

The mortar samples of the Castle of Cannero (Lake Maggiore, Italy) have been characterized and radiocarbon (14C) dated. The presence of LDH phases was identified. The hydraulic reaction was evaluated by a multi-analytical approach. Careful extraction, preparation and purification of the binder fraction have been performed. Contaminations due to LDH phases have been removed allowing reliable absolute dating of the structures.

Non-hydraulic lime-based mortars represent only part of the binding materials found in archaeological and historical structures, and a new challenge is the application of 14C dating techniques on mortars that feature hydraulic reactions. This research work aims at 14C dating a series of Mg-rich hydraulic mortars from the Castle of Cannero (Lake Maggiore, Italy), from which both charcoals and mortar samples were collected. A multi-analytical approach employing X-ray powder diffraction (XRPD), optical microscopy (OM), and scanning electron microscopy/energy-dispersive microanalysis (SEM-EDS) was adopted in order to carefully characterize the samples. A wet gravimetric separation for the extraction of the fine fraction mainly composed by the mortar binder was carried out and the binder fraction was characterized by XRPD in order to investigate the presence of contaminants. The binding fractions are characterized by the widespread occurrence of hydrotalcite-type minerals, considered contaminants in 14C dating of mortars because of their capability to exchange carbonate anions even after the hardening process. A further purification treatment by thermal decomposition was performed before 14C dating by AMS. The obtained dates were consistent with archaeological expectations, confirming the potential of the developed purification methodology for hydraulic mortars dating.

Lead carbonates were used as cosmetic and pigment since Antiquity. The pigment, known as lead white, was generally composed of cerussite and hydrocerussite. Unlike most ancient pigments, lead white was obtained by a synthetic route involving metallic lead, vinegar and organic matter. Fermentation of organic matter produces heat and CO2 emission, leading to the formation of carbonates. As lead white is formed by trapping CO2, radiocarbon (14C) dating can thus be considered. We have developed a protocol to prepare lead white. We selected modern pigments for the experiment implementation and ancient cosmetic and paintings for dating. After characterization of the samples by XRD, thermal decomposition of cerussite at various temperatures was explored in order to select the appropriate conditions for painting samples. CO2 extraction yield, SEM and XPS were used to characterize the process. Thermal decomposition at 400°C was successfully applied to mixtures of lead white with other paint components (oil as binder, calcite as filler/extender) and to historical samples. We obtained radiocarbon measurements in agreement with the expected dates, demonstrating that thermal decomposition at 400°C is efficient for a selective decomposition of lead white and that paintings can be directly 14C-dated by dating lead white pigment.

Data on the dehydration of pentahydroborite, CaB2O(OH)6·2H2O and nifontovite, Ca3B6O6(OH)12·2H2O from the Fuka mine, Japan are presented. Critical temperatures of the dehydration of the borates were determined by thermogravimetric analysis/differential thermal analysis measurements. The untreated mineral samples and their heating products were investigated by X-ray diffraction and Raman spectroscopy. Upon dehydration, both minerals decompose and undergo amorphization, and at greater temperatures crystallize as an orthorhombic calcium borate, CaB2O4 (Pnca). The dehydration paths of the two minerals are different, with nifontovite showing a greater resistance to decomposition and amorphization than pentahydroborite. Differences in the dehydration processes are related to the residuals of the water content and structural accommodation of the borate polyanion.

Previous work on the structural and thermal properties of various types of kaolinite have led to different conclusions, rendering comparison of analytical results difficult. The objectives of the present study were to investigate the thermal behaviour of kaolinite and to carry out a kinetic analysis of the decomposition of kaolinite at high temperatures. X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FTIR) and thermogravimetry-differential scanning calorimetry (TG-DSC) were used to study the mechanism of the thermal decomposition. The modified Coats–Redfern, Friedman, Flynn–Wall–Ozawa and Kissinger decomposition models were used to determine the decomposition mechanism of the kaolinite sample. The dehydroxylation of kaolinite occurred at ∼600°C with the formation of metakaolin, which then transformed into either γ-alumina or aluminium-silicon spinel together with amorphous silica. The results of the XRD and FTIR analyses indicated that the γ-alumina, or aluminium-silicon spinel and amorphous silica phases, transformed into mullite and α-cristobalite, respectively, after decomposition at 900°C. Good linearity was observed with the modified Coats–Redfern, Flynn–Wall–Ozawa and Kissinger models from room temperature to 1400°C and the range of the activation energy determined was 120–180 kJ/mol.

This study examines how to stop the pyrolysis of fir needles, birch leaves, aspen twigs and their mixture using the minimum volumes of water. The combustion of forest fuels is suppressed by spraying water on their surface. The temperature of thermal decomposition is monitored throughout the layer of forest fuel by thermocouples. A high-speed camera and optical techniques allow us to study water spraying and its interaction with forest fuels. Finally, the study specifies the ranges of the minimum water volumes and the times of ending of the thermal decomposition of forest fuels. When analyzing the energy balance in the thermally decomposing forest fuel, a mathematical expression is formulated to predict the water volume sufficient to suppress thermal decomposition of forest fuel. This expression takes into account the ratio between the heat energy spent on water evaporation in pores of forest fuel and the heat energy of the reacting layer of forest fuel. The obtained dimensionless factor considers the main parameters of water spraying and the properties of forest fuel. This factor enables us to apply the research findings to forest fuel in various regions of the world.