Thermal Scanning Research Articles

Effect of al content on microstructure and corrosion resistance of Zn-Al-Mg alloy

In order to solve the solidification microstructure of Zn-1.7Al-1.1Mg alloy on the surface of steel plate during hot dip plating, the solidification path and microstructure of Zn-1.7Al-1.1Mg alloy were studied by Thermo-Calc thermodynamic software, differential thermal analysis (DSC) and scanning electron microscopy (SEM). The results show that during cooling from melting to room temperature, Zn-1.7Al-1.1Mg alloy begins to precipitate Zn-rich η phase at 386.5 °C, binary eutectic structure consisting of η phase and Mg2Zn11 at 350.0 °C, and ternary eutectic structure consisting of η phase, Al-rich metastable β phase and Mg2Zn11 at 343.4 °C,at 276.7 °C, β phase transforms into stable aluminum-rich α and η phases.

Enhanced lead adsorption by eco-hydroxyapatite derived from marble sludge: Optimization and kinetic study

In this study, eco-hydroxyapatite (e-HAP) was synthesized from marble sludge via a hydrothermal process for utilization as an adsorbent in the removal of Pb2+ ions from wastewater. X-ray powder diffraction (XRD) and thermal field emission scanning electron microscope (FE-SEM) revealed that increasing the Ca/P molar ratio (CPMR) and hydrothermal temperature (HT) increased crystallinity and that the influence of HT was more apparent. An increase in crystallinity, crystal length, and peak intensity was observed following an increase in the CPMR. Adsorption studies show that when the HT was 393 K, the CPMR was 0.67, the initial Pb2+ ion concentration was 100 mg/L, the equilibrium time was 20 min, and the adsorbent dosage was 0.6 g/L. The resulting removal efficiency (99.99 %) and maximum adsorption capacity (166.65 mg/g) are both very high. Adsorption kinetics are well described using a pseudo-second-order kinetic model. This paper presents a facile and economically sustainable approach to the synthesis of e-HAP from marble sludge for use in removing of Pb2+ from wastewater.

Synthesis of copper-doped nanocrystalline tin stannate by thermal decomposition of a precursor

Zinc hydroxostannate ZnSn(OH)6, containing 5 mol.% Cu, was obtained from hydrochloric acid solutions of tin(IV), zinc and copper by adding sodium hydroxide to pH = 8–9. The thermolysis process of the obtained sample and the phase composition of the decomposition products were studied using thermal analysis, X-ray diffraction, and scanning electron microscopy. It was shown that the main stages of dehydration are completed at a temperature of about 350 °C and, as a result of thermolysis, an X-ray amorphous product is formed, from which a solid solution of copper in zinc stannate is obtained at an annealing temperature above 650 °C. At an annealing temperature of 800 °C, a mixture of nanocrystalline tin dioxide SnO2 with a cassiterite structure and copper-doped zinc orthostannate Zn2SnO4 with a spinel structure is formed. The room temperature sensors based on ZnSnO3 and carbon nanofibers as a conductive additive showed high response to NO2 (–6.1% to 2 ppm NO2).

Unlocking the secrets of Neapolitan pizza: A concise review of wood-fired, electric, and gas pizza ovens.

This review explores the Neapolitan pizza baking process in a traditional wood-fired oven, employing visual color analysis and IR thermal scanning to detail heat exchange mechanisms. During cooking, the oven floor temperature in the pizza area decreased proportionally to the pizza's mass, whereas the free area maintained a constant temperature of 439±3°C. An IR thermal camera indicated that the oven dome temperature reached approximately 480°C with a weak flame and 500°C with a strong flame. The pizza's bottom achieved a maximum temperature of 100±9°C, facilitated by the Pizzaiolo's skill in lifting and rotating the pizza for uniform cooking. Top temperatures varied: up to 180°C for white pizza and 84°C and 67°C for tomato and Margherita pizzas, respectively. IRIS electronic eye analysis revealed more browning and blackening on the pizza's top compared to its bottom, with peaks of about 26% and 8% for white pizza, respectively. Rapid baking is pivotal in Neapolitan pizza-making, necessitating precise heat and mass transfer management to influence sensory attributes. European Commission Regulation No. 97/2010 mandates wood-fired ovens for true Neapolitan pizza, but environmental concerns prompted the Associazione Verace Pizza Napoletana to certify gas or electric ovens when wood-fired ovens are impractical. Operating costs vary: liquefied petroleum gas ovens are the costliest, with costs ranging from €5.38 to €6.19/h, whereas natural gas and electric ovens have operating costs between €2.70 and €4.10/h. At €0.15/kg, firewood is the most economical, supporting traditionalist views. However, natural gas and electric ovens present competitive costs under stringent antipollution laws, making them viable alternatives.

Enhanced Sinterability and Mechanical Strength of Beta-type Tricalcium Phosphates Ceramics through Reaction Sintering with Hydroxyapatite

Beta-tricalcium phosphate (β-TCP) ceramics were fabricated via reaction sintering at 1100 °C, utilizing various phosphate salts and calcium compounds as raw materials. The sintering characteristics, reaction sintering behavior and mechanical properties of the resulting β-TCP ceramics were investigated. Reaction sintering with a Ca/P molar ratio of 1.50 consistently generated β-TCP. In addition, a notable variance in physical properties was observed contingent on the presence or absence of stoichiometric hydroxyapatite (HAp; Ca10(PO4)6(OH)2) in raw materials. Sintered bodies produced with HAp−β-Ca2P2O7 (β-CPP), HAp− CaHPO4·2H2O (DCPD) and HAp−(NH4)2H(PO4) all exhibited densification and enhanced mechanical strength, correlated with higher bulk densities. In contrast, conventional sintered bodies prepared from β-TCP and reaction sintered bodies prepared using β-CPP−Ca(OH)2 or β-CPP−CaCO3 were not as dense. Comprehensive assessments by thermogravimetry-differential thermal analysis, X-ray diffraction and scanning electron microscope together with the evaluation of shrinkage behavior were used to monitor the sintering of β-TCP with HAp. This process was found to involve thermal decomposition of HAp and crystal transitions leading to the formation and sintering of β-TCP with significant shrinkage. These findings underscore the efficacy of employing HAp as a raw material in reaction sintering. This technique allows the formation of sintered β-TCP bodies exhibiting exceptional sintering characteristics, superior bulk density and high mechanical strength.

A General Method for Calibration of Active Scanning Thermal Probes

Scanning thermal microscopy (SThM) is a scanning probe technique aimed at quantitative characterization of local thermal properties at the length scale down to tens of nanometers. With many probe designs and approaches to interpretation of probe responses, there is a need for a universal framework, which would allow probe calibration and comparison of probe performance. Herein, a calibration framework based on an abstracted, formal, probe model for active SThM probes is developed. The calibration can be accomplished through measurements with two or three calibration samples. Requirements for calibration samples are described with examples of structures of suitable samples identified in published literature. A link to a published experimental work indirectly verifying the proposed procedure is provided. The calibration does not require knowledge of internal probe properties and yields a small and universal set of parameters that can be used to quantify thermal resistance presented to the probe by samples as well as to characterize active‐mode SThM probes of any type and at any measurement frequency. How the probe calibration parameters can be used to guide probe design is illustrated. When the calibration approach can be used directly to measure the thermal conductivity of unknown samples is also analyzed.

Antifouling ultrafiltration membranes based on acrylic fibers waste/nanochitosan for Congo red and crystal violet removal

AbstractIn this study, acrylic fibers waste blended with different ratios of nanochitosan (0.5%, 1%, 2% and 4%, in weight) were converted into antifouling ultrafiltration nanocomposite membranes using a phase separation technique for the remediation of Congo red (CR) and crystal violet (CV) dyes from water. The fabricated nanocomposite membranes were investigated using Fourier Transform Infrared (FTIR), thermal gravimetric analysis (TGA), X-ray diffraction (XRD) and scanning electron microscope (SEM). The membrane hydrophilicity was estimated using contact angle measurements, which revealed that the 4% loaded nanochitosan had the highest hydrophilicity. Additionally, the water uptake, porosity, water contact angle and water flux of the nanocomposite membranes were assessed. The membrane filtration performances were explored for the removal of CR and CV as anionic and cationic dyes, respectively, at different concentrations and various applied pressures (1 bar to 4 bar). The experimental data revealed a high rejection (R) performance for CR (R≃100%) with a high water flux of about 150 L/(m2·h) to 183 L/(m2·h) for the optimized membrane with 2% nanochitosan at an applied pressure of 4 bar. The rejection for CV showed a variant rejection (70%–99%) at different dye concentrations with fluxes ranging from 93.6 L/(m2·h) to 149.5 L/(m2·h) for the same composite membrane. The composite membrane showed enhanced flux recovery after fouling by bovine serum albumin and was resistant to widespread gram-positive (Staphylococcus aureus) bacteria. Graphical abstract

Assembly and Bilayer Liftoff of Periodic Nanostructures with Sub-20 nm Resolution Using Thermal Scanning Probe Lithography

Assembly and Bilayer Liftoff of Periodic Nanostructures with Sub-20 nm Resolution Using Thermal Scanning Probe Lithography

Geothermal Nano-SiO2 Waste as a Supplementary Cementitious Material for Concrete Exposed at High Critical Temperatures.

The partial replacement effect of Portland cement by geothermal nano-SiO2 waste (GNSW) for sustainable Portland-cement-based concrete was investigated to improve the properties of concrete exposed at high critical temperatures. Portland cement was partially replaced by 20 and 30 wt.% of GNSW. The partial replacement effect on Portland-cement-based concrete subjected to 350, 550, and 750 °C was evaluated by measuring the weight changes, ultrasonic pulse velocity, thermogravimetric and differential thermal analysis, X-ray diffraction, surface inspection, and scanning electron microscopy under residual conditions. The ultrasonic pulse velocity results showed that the GNSW specimens maintained suitable stability after being heated to 350 °C. The SEM analysis revealed a denser microstructure for the 20 wt.% of partial replacement of Portland cement by GNSW specimen compared to the reference concrete when exposed to temperatures up to 400 °C, maintaining stability in its microstructure. The weight losses were higher for the specimens with partial replacements of GNSW than the reference concrete at 550 °C, which can be attributed to the pozzolanic activity presented by the GNSW, which increases the amounts of CSH gel, leading to a much denser cementitious matrix, causing a higher weight loss compared to the reference concrete. GNSW is a viable supplementary cementitious material, enhancing thermal properties up to 400 °C due to its high pozzolanic activity and filler effect while offering environmental benefits by reducing industrial waste.

Autonomous post‐disaster indoor navigation and survivor detection using low‐cost micro aerial vehicles

AbstractThis paper introduces an innovative autonomous survivor detection pipeline tailored for low‐cost micro aerial vehicles (MAVs) operating in post‐disaster indoor environments. This consists of three main components: (1) a novel pipeline for survivor geotagging, which includes autonomous navigation, mapping, and detection of survivors using thermal images; (2) a navigation strategy to ensure complete thermal scanning coverage for survivor detection using low‐cost commercial grade thermal camera; and (3) robust and accurate survivor detection using YOLOv8x and thermal imaging. To demonstrate the effectiveness of the proposed framework, first, the autonomous navigation algorithm is simulated in Robotic Operating System (ROS) and experimentally validated under different layouts. Second, the YOLOv8x algorithm is pretrained and achieves high accuracy. Finally, a real‐world implementation was conducted with partially covered survivors in a simulated post‐disaster environment. The results demonstrated the proposed pipeline can accurately map the layout of the environment and identify all survivors. This study demonstrates that affordable MAVs with basic thermal cameras can be effectively used to geotag survivors to support rescue missions during post‐disaster events.

Exploring of new Poly(Thiourea-Amide) as a prospective bismarck Brown Y dye adsorbent: Synthesis via ultrasound irradiation, isotherms, kinetic, thermodynamic, and DFT studies

In this work, a facial ultrasound technique was employed to synthesize poly (N1-((6-aminopyridin-2-yl)carbamothioyl)-N3-carbamothioylisophthalamide) (PTUA) as a new polymer from a condensation reaction of isophthaloyl diisothiocyanate and 2, 6-diaminopyridine. Different techniques were utilized to identify the chemical structure of the synthesized polymer including FTIR spectra, 1HNMR spectra, thermal gravimetric analysis (TGA), Brunauer-Emmett-Teller (BET), and field emission scanning electron microscopy (FESEM). The capability of the synthesized polymer to adsorb Bismarck brown Y (BBY) dye from an aqueous solution was analytically evaluated. Several effective parameters on the adsorption process including contact time, pH, dye concentration, adsorbent dose, and temperature were extensively investigated. The adsorption process was found to be completed with a contact time of 45 min. The results indicated that the optimal adsorption pH was 8 with removal efficiency of 85.331 % and the adsorbed amount of BBY dye increased when the temperature was increased. The adsorption isotherms analysis revealed that the Langmuir model with a correlation coefficient (R2 = 0.9982) was the most relevant to describe the adsorption process compared with the Freundlich model (R2 = 0.9863). By applying the Langmuir isotherm, the maximum adsorption capacity was obtained with a value of 132.39 mg/g. The study of adsorption kinetics showed that the adsorption model of BBY dye onto the polymer surface significantly correlated with a pseudo-second-order model. Based on the thermodynamic studies, the calculated ΔG was negative, ΔH was endothermic, and ΔS was positive, verifying the adsorption process is spontaneous. The desorption percentage of BBY dye was calculated with a value of 81.574 % utilizing methanol as an optimal solvent. The density functional theory (DFT) approach was applied to acquire good understanding for the adsorption process.

Nanoscale Heat Transport of Vertically Aligned Carbon Nanotube Bundles for Thermal Management Applications.

Electronic devices continue to shrink in size while increasing in performance, making excess heat dissipation challenging. Traditional thermal interface materials (TIMs) such as thermal grease and pads face limitations in thermal conductivity and stability, particularly as devices scale down. Carbon nanotubes (CNTs) have emerged as promising candidates for TIMs because of their exceptional thermal conductivity and mechanical properties. However, the thermal conductivity of CNT films decreases when integrated into devices due to defects and bundling effects. This study employs a novel cross-sectional approach combining high-vacuum scanning thermal microscopy (SThM) with beam-exit cross-sectional polishing (BEXP) to investigate the nanoscale morphology and thermal properties of vertically aligned CNT bundles at low and room temperatures. Using appropriate thermal transport models, we extracted effective thermal conductivities of the vertically aligned nanotubes and obtained 4 W m-1 K-1 at 200 K and 37 W m-1 K-1 at 300 K. Additionally, non-negligible lateral thermal conductance between CNT bundles suggests more complex heat transfer mechanisms in these structures. These findings provide unique insights into nanoscale thermal transport in CNT bundles, which is crucial for optimizing novel thermal management strategies.

Synthesis and characterization of novel double perovskite K2AgBiBr6

Over the past few years, Lead-free halide double perovskites have attracted a tremendous attention such that it is demonstrated by the power conversion efficiency's sharp increase of over 25 %. It has also stimulated a widespread application of halide metal perovskites in other fields, such as light-emitting diodes, field-effect transistors, detectors, and lasers. Double perovskites have been put forth as an alternative to hybrid lead halide perovskites in the last decade because of their efficiency in doing away with the existing toxicity and instability. It is probably the first attempt, to date, that lead-free halide double perovskite K2AgBiBr6 has been made with a cheap, easy-to-use solution-state reaction method. To determine their structure, single crystal X-ray diffraction and PXRD analysis have been employed. The synthesized K2AgBiBr6 adopts the cubic structure with Fm‾3m symmetry and lattice parameters of a = 6.606 (9) Å at room temperature, according to the diffraction result. Energy dispersive X-ray spectroscopy (EDX), elemental mapping, and scanning electron microscopy (SEM) have all been employed to analyze the morphology and elemental composition. Elements including K, Bi, Ag, and Br have been confirmed to be present in the synthesized sample by the EDX technique. For K2AgBiBr6, the 2.859 eV (indirect) and 3.076 eV (direct) bandgaps have been estimated by employing the UV–Vis absorption spectra. Furthermore, the K2AgBiBr6 double perovskite nanocrystal's thermogravimetric analysis/differential thermal and differential scanning analysis (TG/DTA and DSC) curves at 20–800 °C have been measured. An analysis has been conducted on the mechanism of thermal decomposition of synthesized double perovskite. This work demonstrates great promise for future band gap engineering-based photovoltaic and other optoelectronic applications, and it offers a novel path to obtaining premium K2AgBiBr6 double perovskite.

Study on microstructure and thermal shock resistance of plasma sprayed Cr2O3/8YSZ composite coating

In order to explore the high temperature performance of Cr2O3/8YSZ composite coating, four kinds of Cr2O3/8YSZ composite coatings were prepared on the surface of Q235 steel by using the plasma spraying technology (the content of 8YSZ is 50%, 30%, 20% and 0%, respectively). The morphology of the coating was characterized through thermal field emission scanning electron microscopy, and the distribution of elements in the section of the coating was scanned by using EDS line. The phase composition of the composite coating was analyzed by using X-ray diffractometer, and the surface roughness of the composite coating was measured by using surface profilometer. The microhardness of the coating was measured by using automatic micro-Vickers hardness tester, and the scratch resistance of the coating was compared by using scratch tester. The thermal shock resistance of the coating was tested in Gleeble-3800 thermal physical simulator, and the cross section morphology after thermal shock was observed and analyzed. The results show that when the ratio of Cr2O3 to 8YSZ is 7∶3, the sample coating has good thermal shock resistance due to the deflection effect of 8YSZ on the vertical cracks and the thermal stress release effect of the pores and cracks in the coating.

Comparison of hand, rotary, reciprocating and self-adjusting files in cleaning mesio-buccal canals of maxillary first molars.

The smear layer removal capability of different instrumentation techniques on the mesio-buccal root canals of maxillary first molars is of interest to dentists. Sixty extracted maxillary first molars with fully developed apices, curved root canals, and curvatures between 30 to 45 degrees were selected. The teeth were divided into four groups (n=15) based on the instrumentation technique used. The samples were analyzed using a thermal field emission scanning electron microscope to assess smear layer removal at the apical, middle, and coronal thirds of the canals. The Wave One file system showed superior performance in smear layer removal across all three regions of the canal compared to hand files, Hyflex CM rotary files and SAF.

Effect of Alkyl Side Chains in BDT and 2D‐BDT Small‐Molecules as Donor Materials for Vacuum‐Processed Organic Photovoltaic Devices

Nine molecules based on benzo[1,2‐b:4,5‐b′]dithiophene (BDT) and 2D‐BDT derivatives are studied as donor materials in organic photovoltaic (OPV) devices fabricated by thermal evaporation, aiming to understand how different alkyl lateral substituents affect the molecular packing, the charge transport, and, subsequently, the device performance. Synthesis of the molecules is followed by a comprehensive characterization using thermal and differential scanning calorimetry analyses, which confirm their thermal stability and suitability for vacuum‐processed OPV devices. Thermal analysis also demonstrates a strong correlation between the melting point reduction of the molecules and the disorder caused by the alkyl chains. As the synthesized molecules present similar optical properties, the differences in the device performance are caused by the different substituents. BDT derivatives with low melting point temperatures produce reduced current density, hole mobility, and overall device performance, which are attributed to poor molecular packing. Additionally, energy‐dispersive X‐ray spectroscopy analysis suggests phase separation with fullerene, further impacting the efficiency of the devices. The findings indicate that the photovoltaic performance of BDT‐based molecules can be modulated by avoiding aliphatic substituents, providing a strategy for the design of more efficient materials, with thermal evaporation as an ideal method to evaluate and decouple molecular packing from solubility.

The Relation between Soil Moisture Phase Transitions and Soil Pore Structure under Freeze–Thaw Cycling

The process of soil moisture phase transitions (SMPT) under freeze–thaw cycling is considered a key factor driving changes in soil pore structure. However, there is still no consensus on which indicators related to SMPT affect the soil pore structure. The objectives of this study were to compare SMPT and soil pore characteristics under freeze–thaw cycling, and to analyze the inherent relationship between them as affected by different bulk densities. Hence, we employed thermal pulse time-domain reflection technology (T-TDR) and X-ray CT scanning technology (X-CT) to quantitatively study the process of SMPT and pore characteristics of soil core samples (60 mm diameter, 100 mm height) repacked with three different bulk density levels: 1.10 g·cm−3 (NC), 1.30 g·cm−3 (LC) and their combination (1.10 g·cm−3 for upper half, 1.30 g·cm−3 for lower half, SC) under freeze–thaw cycling. Our results showed that compared with NC, the porosity of LC’s 0–5 cm soil column decreased by 0.070 cm3·cm−3, the imaged porosity (ϕ>60μm) decreased by 0.034 cm3·cm−3, and the maximum soil ice content (MIC) decreased by 0.030 cm3·cm−3. The pores within the range of 200−300 mm (ϕ2) and 300–400 mm (ϕ3) contribute the most significantly to ϕ>60μm (50–60%). Soil initial moisture content (IMC) and MIC explained 50.1% of the change in ϕ2, and the bulk density explained 49.3% of the change in ϕ3. During the melting process, higher moisture content promotes the thaw collapse of soil particles, resulting in a decrease in ϕ>60μm. The mean pore radius of the limiting layer (MRLL) and the hydraulic radius (HR) show that changes in bulk density from 1.10 g·cm−3 to 1.30 g·cm−3 do not have significant differences. Our results show the relationship between SMPT and pore structure change during freeze–thaw cycles as affected by initial soil bulk density and moisture condition.

Thermal energy storage performance of liquid polyethylene glycol in core–shell polycarbonate and reduced graphene oxide fibers

Thermal energy storage is a promising, sustainable solution for challenging energy management issues. We deploy the fabrication of the reduced graphene oxide (rGO)–polycarbonate (PC) as shell and polyethylene glycol (PEG) as core to obtain hydrophobic phase change electrospun core–shell fiber system for low-temperature thermal management application. The encapsulation ratio of PEG is controlled by controlling the core flow rate, and ~ 93% heat energy storage efficacy is apparent for 1.5 mlh−1 of core flow rate. Moreover, the prepared fiber possesses maximum latent melting and freezing enthalpy of 30.1 ± 3.7 and 25.6 ± 4.0 Jg−1, respectively. The transient dynamic temperature vs. time curve of the rGO-loaded phase change fiber demonstrates the delay of fiber surface temperature change compared to pristine fiber. We indeed show that the tunable heat transfer and thermal energy storage efficacy of phase change fiber is achieved via controlled liquid PEG delivery and the addition of rGO in shell architecture. Notably, the effectiveness of unique phase change material (PCM)–based core–shell fibers is concluded from advanced scanning thermal microscopy (SThM) and self-thermoregulation tests.

Unraveling the Impact of Boron Nitride and Silicon Nitride Nanoparticles on Thermoplastic Polyurethane Fibers and Mats for Advanced Heat Management.

The urgent challenges posed by the energy crisis, alongside the heat dissipation of advanced electronics, have embarked on a rising demand for the development of highly thermally conductive polymer composites. Electrospun composite mats, known for their flexibility, permeability, high concentration and orientational degree of conductive fillers, stand out as one of the prime candidates for addressing this need. This study explores the efficacy of boron nitride (BN) and its potential alternative, silicon nitride (SiN) nanoparticles, in enhancing the thermal performance of the electrospun composite thermoplastic polyurethane (TPU) fibers and mats. The 3D reconstructed models obtained from FIB-SEM imaging provided valuable insights into the morphology of the composite fibers, aiding the interpretation of the measured thermal performance through scanning thermal microscopy for the individual composite fibers and infrared thermography for the composite mats. Notably, we found that TPU-SiN fibers exhibit superior heat conduction compared to TPU-BN fibers, with up to a 6 °C higher surface temperature observed in mats coated on copper pipes. Our results underscore the crucial role of arrangement of nanoparticles and fiber morphology in improving heat conduction in the electrospun composites. Moreover, SiN nanoparticles are introduced as a more suitable filler for heat conduction enhancement of electrospun TPU fibers and mats, suggesting immense potential for smart textiles and thermal management applications.

Supramolecular interactions in cocrystals of benzoic acid derivatives with selective COX-2 inhibitor etoricoxib.

The structures of three 1:1 cocrystal forms of etoricoxib {ETR; systematic name: 5-chloro-2-(6-methylpyridin-3-yl)-3-[4-(methylsulfonyl)phenyl]pyridine, C18H15ClN2O2S} have been synthesized and characterized by single-crystal X-ray diffraction; these are etoricoxib-benzoic acid (1/1), C18H15ClN2O2S·C7H6O2 (ETR-Bz), etoricoxib-4-fluorobenzoic acid (1/1), C18H15ClN2O2S·C7H5FO2 (ETR-PFB), and etoricoxib-4-nitrobenzoic acid (1/1), C18H15ClN2O2S·C7H5NO4 (ETR-PNB). Powder X-ray diffraction and thermal differential scanning calorimetry-thermogravimetry (DSC-TG) techniques were also used to characterize these multicomponent systems. Due to the influence of the corresponding acids, ETR shows different conformations. Furthermore, the energetic contributions of the supramolecular motifs have been established by energy framework studies of the stabilizing interaction forces and are consistent with the thermal stability of the cocrystals.