Heating Ramp Research Articles

Thermo-diffusion of excited photothermal semiconductor under laser pulse and ramp heating with acoustic pressure

The goal of this work is to provide a novel mathematical model that explains how certain physical variables propagate (acoustic-thermal-mechanical diffusive) as waves in a photoexcited non-Gaussian laser pulse semiconductor medium. Under the impact of acoustic pressure, the isotropic and homogeneous semiconductor medium is discussed concerning the fundamental equations according to charge carrier recombination processes with optoelectronic properties. Given the impact that relaxation times have on the governing equations. Laplace transforms were utilized in a one-dimensional (1D) context to examine essential non-dimensional properties such as displacement, stress components, carrier density, temperature, and acoustic pressure in order to mathematically answer the required problem. By imposing specific initial and boundary conditions, inverse Laplace transformations were employed to generate precise solutions for the numerical modeling of different physical quantities depicted graphically. The graphical representation of wave propagation data was followed by a theoretical analysis and interpretation, emphasizing the influence of other factors (such as heat rise time, relaxation times, and laser pulse effects) on the observed occurrences.

Transformations in laser track microstructures for a quasicrystal-reinforced Al-Cu-Fe-Cr alloy

Aluminum-quasicrystal composites are attractive candidate alloys for additive manufacturing, but the cost of evaluating such systems can be prohibitive. Recently, surface laser glazing studies have been used to show that desirable composite microstructures can be formed in an Al85Cu6Fe3Cr6 alloy under a wide range of laser processing parameters. Here the thermal stability of these laser track microstructures has been evaluated by performing in situ scanning transmission electron microscopy heating experiments on specimens produced by focused ion beam milling from the center of the tracks. The initial track microstructures exhibited a uniform phase mixture with 70 % by volume of I-phase quasicrystalline dispersoids in a FCC Al matrix with a film of Al2Cu at the interface. Preliminary ramped heating experiments were used to identify the temperatures at which transformations occurred and then isothermal experiments on fresh samples were used to monitor the progress of these processes. For temperatures of up to 450 °C the only significant changes were a redistribution and coarsening of the Al2Cu phase with a gradual increase in the Fe content of the phase. At higher temperatures, the I-phase decomposed to form a mixture of crystalline ω-Al7Cu2Fe and μ-Al4Cr phases. The I-phase decomposition proceeded by ejection of Cu and Fe with the remaining Cr-rich regions transforming to the Al4Cr approximant phase. The implications of these phenomena for use of the alloy in additive manufacturing are discussed.

Thermal transformations of perfluorooctanoic acid (PFOA): Mechanisms, volatile organofluorine emissions, and implications to thermal regeneration of granular activated carbon

Thermal treatment is effective for the removal of perfluorooctanoic acid (PFOA). However, how temperatures, heating methods, and granular activated carbon (GAC) influence pyrolysis of PFOA, and emission risks are not fully understood. We studied thermal behaviors of PFOA at various conditions and analyzed gaseous products using real-time detection technologies and gas chromatography-mass spectrometry (GC-MS). The thermal decomposition of PFOA is surface-mediated. On the surface of quartz, PFOA decomposed into perfluoro-1-heptene and perfluoro-2-heptene, while on GAC, it tended to decompose into 1 H-perfluoroheptane (C7HF15). Neutral PFOA started evaporating around 100 ℃ without decomposition in ramp heating. During pyrolysis, when PFOA was pre-adsorbed onto GAC, it was mineralized into SiF4 and produced more than 45 volatile organic fluorine (VOF) byproducts, including perfluorocarbons (PFCs) and hydrofluorocarbons (HFCs). The VOF products were longer-chain (hydro)fluorocarbons (C4-C7) at low temperatures (< 500 ℃) and became shorter-chain (C1-C4) at higher temperatures (> 600 ℃). PFOA transformations include decarboxylation, VOF desorption, further organofluorine decomposition and mineralization in ramp heating of PFOA-laden GAC. Decarboxylation initiates at 120 ℃, but other processes require higher temperatures (>200 ℃). These results offer valuable information regarding the thermal regeneration of PFAS-laden GAC and further VOF control with the afterburner or thermal oxidizer.

Synthesis, characterization, and performance evaluation of unsupported tetrametallic CoMoMnAl and CoMoZnAl catalysts for selective hydrodesulfurization (HDS)

New formulations of unsupported tetrametallic catalysts derived from layered double hydroxides (LDH) compounds were synthesized by a constant pH coprecipitation method, characterized, and evaluated in the selective hydrodesulfurization (HDS) of thiophene in the presence of cyclohexene. The layered double hydroxides were prepared using terephthalate (C8H8O2)2- as the interlayer anion with nominal aluminum molar fraction of 0.5, and nominal cobalt to MII (M = Zn or Mn) ratios of 0.2, 0.4 and 0.6. Molybdenum introduction in the LDH precursor was accomplished by an ion exchange process using the heptamolybdate anion. The calcined Mn samples showed a higher surface area than those obtained from Zn. The sulfidation was carried out in situ with a heating ramp up to 673 K and the catalysts were evaluated in a tubular flow reactor. The catalytic evaluation of Zn and Mn-based materials for simultaneous thiophene HDS and cyclohexene hydrogenation (HYD) was conducted at 573 K and 20 bar. The results show that the Zn-based unsupported catalysts synthesized here exhibited higher selectivity for the HDS reaction than an industrial one.

Spark plasma sintering of hard wear‐resistant graphene nanoplatelet–reinforced TiB2 + SiC composites from TiC–B4C–SiC

AbstractGraphene nanoplatelet (GNP)–reinforced TiB2 + SiC composites were fabricated by reactive spark plasma sintering (SPS) from a TiC–B4C–SiC powder mixture with equal‐volume percentages, optimizing their SPS temperature and evaluating their unlubricated sliding wear against diamond. First, it is shown that during the heating ramp of the SPS cycle, TiC and B4C react according to the chemical reaction 2TiC + B4C → 2TiB2 + 3C, and that the thus‐formed C is graphenized as GNPs, leading to composites with microstructures consisting of a ceramic matrix of fine TiB2 and SiC grains with abundant randomly oriented GNPs at grain boundaries. It is also shown that this reactive SPS is optimal at 2000°C (under 75 MPa pressure and 5 min soaking), resulting in a very hard (∼28.5–29.9 GPa) and very tough (∼6.7(3) MPa m1/2) composite. And second, it is shown that these two properties and its proneness to develop an oxide tribolayer make this composite very resistant to unlubricated sliding wear against diamond (∼2.8(1)·108 (N m)/mm3), undergoing only very mild two‐body abrasion. Finally, opportunities for the fabrication of toughened and very hard ceramic composites for contact‐mechanical and tribological applications are discussed.

Monitoring the evolution of optical coatings during thermal annealing with real-time, in situ spectroscopic ellipsometry

Abstract Thermal annealing plays a key role in optimizing the properties of amorphous optical coatings. In the field of gravitational wave detection (GWD), however, the effects of annealing protocols on the interferometry mirror coatings have been explored primarily by ex post analysis. As a result, the dynamics of the coatings properties during annealing is still poorly known, potentially leading to suboptimal performance. Here, using real-time, in situ spectroscopic ellipsometry (SE) we have tracked the refractive index and thickness of a titania-tantala coating during controlled annealing. We have tested the material and the annealing protocol used in&amp;#xD;current GWD mirrors. The annealing cycle consisted of a heating ramp from room temperature to 500 °C, followed by a 10-hour plateau at the same temperature and the final cooling ramp. SE measurements have been run continuously during the entire cycle. Significant variations in the thickness and refractive index, which accompany the coating structural relaxation, have been recorded during the heating ramp. These variations start around 200 °C, slightly above the deposition temperature, and show an increased rate in the range 250-350 °C. A smaller, continuous evolution has been observed during the 10-hour high-temperature plateau. The results offer&amp;#xD;suggestions to modify the current annealing protocol for titania-tantala coatings, for example by increasing the time duration of the high-temperature plateau. They also suggest an increase in the substrate temperature at deposition. The approach presented here paves the way for systematic, real-time investigations to clarify how the annealing parameters shape the properties of optical coatings, and can be leveraged to define and optimize the annealing protocol of new candidate materials for GWD mirrors.

Co3O4@SiO2 3D Monolith Catalysts, Additive Manufactured Structures for Propane Oxidation Reaction

AbstractIn this study, we successfully fabricated a three‐dimensional Co3O4@SiO2 3D Monolith catalyst. This process allowed for the effective and straightforward anchoring of Co3O4 nanoparticles onto SiO2 3D Monoliths. The active Co3O4 phase was primarily identified through XRD and XPS analyses, complemented by Co3O4 loading measurements (1.7 %). This innovative catalyst displayed remarkable proficiency in selectively converting propane to carbon dioxide. Additionally, it was demonstrated that the catalytic activity remained unimpaired even upon the catalyst's reuse in 5 successive reaction cycles. This performance was observed across various heating ramps, showcasing the catalyst's stability over time.

Efficient trihalomethane quantification in drinking water for minimally-equipped water treatment plants labs

Chlorine is a common disinfectant used in water treatment. However, its reaction with organic matter can lead to the formation of harmful byproducts, such as trihalomethanes (THMs), which are potentially carcinogenic. To address this issue, the aim of this work was to enhance a colorimetric method capable of quantifying THMs in drinking water through UV/Vis Spectrophotometry, using cost-effective equipment, and validate this methodology for the first time according to established validation protocols. The method’s innovation involved replacing the solvent pentane with the more common hexane, along with adjusting the heating ramp, elucidating the mechanisms involved in the process. This method involves the reaction between THMs, pyridine, and NaOH to produce a colored compound, which is then monitored through molecular absorption spectroscopy in the visible region. The method was thoroughly validated, achieving a limit of detection of 13.41 μg L−1 and a limit of quantification of 40.65 μg L−1. Recovery assays ranged from 86.1 % to 90.7 %, demonstrating high accuracy. The quality of the linear fit for the analytical curve exceeded R2 > 0.98. The method was applied to real samples, revealing concentrations ranging from 13.58 to 55.46 μg L−1, all way below the legal limit in Brazil (Maximum Contaminant Levels (MCL) = 100 μg L−1). This cost-effective and straightforward method is suitable for integration into water treatment plant laboratories.

Behavior of helium diffusion sinks in apatite: Evidence from continuous ramped heating analysis of borehole and well-characterized samples

Diffusion sinks have been proposed to explain the complex high-temperature 4He release often seen in Continuous Ramped Heating (CRH) analysis of apatites, which often correlates with over-dispersed and anomalously old (U-Th)/He ages. In this work, we first conducted CRH experiments with various ramping rates and cycled CRH experiments that confirm that the high-temperature 4He release from diffusion sinks is systematically temperature sensitive at laboratory time scales. We then analyzed apatite grains from the KTB borehole (German Continental Deep Drilling program) that have well-constrained thermal histories to test whether different thermal histories could alter the trapping of 4He at geologic time scales. The KTB samples show large intra-sample single-grain age dispersion, with most ages being older than predictions from a 4He radiation-damage diffusion model RDAAM. Individual grains from shallower depths show complex 4He outgassing behaviors, including the expected low-temperature volume-diffusion loss, sudden release spikes, and a higher- temperature-dependent component. Grains from the current partial retention zone and greater depths retain considerable helium and exhibit exclusively complex outgassing behavior dominated by high-temperature release in the laboratory. KTB samples show a systematic difference with depth in the proportion of low- and high-temperature gas-release gas components. Deeper samples, having long open-system thermal histories, contain a greater proportion of 4He that appears to have been trapped compared to the simpler volume-diffusion behavior exhibited by shallower samples that experienced a simpler monotonic cooling history. While greatly reduced, the high-temperature component is still present in the highest-temperature samples analyzed, well hotter than the partial retention zone. These observations confirm that in apatite trapping and release of helium from sinks is temperature dependent at geological time scales as well. This supports the suggestion that additional thermal-history information from apatites might be obtained using 4He/3He analysis, with laboratory release of 3He providing information about trap distribution and kinetics and 4He providing information about the geologic thermal history.

Design, development, and performance of a versatile graphene epitaxy system for the growth of epitaxial graphene on SiC.

A versatile graphene epitaxy (GrapE) furnace has been designed and fabricated for the growth of epitaxial graphene (EG) on silicon carbide (SiC) in diverse growth environments ranging from high vacuum to atmospheric argon pressure. Radio-frequency induction enables heating capabilities up to 2000 °C, with controlled heating ramp rates achievable up to 200 °C/s. The details of critical design aspects and temperature characteristics of the GrapE system are discussed. The GrapE system, being automated, has enabled the growth of high-quality EG monolayers and turbostratic EG on SiC using diverse methodologies, such as confinement-controlled sublimation (CCS), open configuration, polymer-assisted CCS, and rapid thermal annealing. This showcases the versatility of the GrapE system in EG growth. Comprehensive characterizations involving atomic force microscopy, Raman spectroscopy, and low-energy electron diffraction techniques were employed to validate the quality of the produced EG.

Evaluation of thermo-fluidic performance of micro pulsating heat pipe with and without evaporator side surface structures

Interfacial behaviour and thermal performance of a 4-loop micro pulsating heat pipe are examined through experiments performed at different filling ratio (30–60 %), working fluid (acetone, ethanol, and methanol), and heat input (0–40 W). During the heat pipe operation, nucleation, growth and merging of bubbles, elongation, and movement of vapor plug, and dry out conditions are noticed upon ramp heating (0–40 W) inside smooth surface evaporator pulsating heat pipe. Experiments show that preparation and boiling inception lead to steady operation of heat pipe. Pulsating heat pipe showed minimum thermal resistance when operated with 40 % filling ratio and acetone as working fluid, which has low viscosity, surface tension and boiling point. Additionally, effect of surface structures (rectangular pillar protrusion and hemispherical dimple cavity) on the evaporator section is tested against base smooth surface micro pulsating heat pipe to understand augmentation of heat transfer. Hemispherical dimple cavities show better nucleation, bubble growth, and vapor plug elongation and thereby reduction in thermal resistance. On the other hand, rectangular pillar protrusions showed clogged bubble, least bubble detachment and vapor plug length in the adiabatic zone which results in higher thermal resistance than even smooth surface.

Screening of Astec® CHIRALDEX™ G-PN and LIPODEX™ D gas chromatography columns for enantioseparation of amphetamine derivatives.

Among different substance classes, New Psychoactive Substances (NPS) comprise chiral amphetamines for stimulant and empathic effects. There is little knowledge in terms of clinical studies about possibly different effects of the two enantiomers of novel amphetamine derivatives. For this reason, there is a big demand for enantioseparation method development of this new substance class. Regarding gas chromatography, cyclodextrins proved to be effective for enantioseparation of NPS. In our attempt, an Astec® Chiraldex™ G-PN column containing 2,6-di-O-pentyl-3-propionyl-γ-cyclodextrin and a Lipodex™ D column containing heptakis-(2,6-di-O-pentyl-O-acetyl)-β-cyclodextrin as chiral selector served as stationary phases in a Shimadzu GCMS-QP2010 SE system. Because of the special coating, maximum temperature is limited to 200 °C isothermal or 220 °C in programmed mode. To ensure detection, trifluoroacetic anhydride (TFAA) was used to increase sample volatility.1 As a result, 35 amphetamines were tested as their TFAA-derivatives. A screening method with a temperature gradient from 140 °C to 200 °C at a heating ramp of 1°C per minute and final time of 5min, showed baseline separation for seven and partial separations for 16 trifluoro acetylated amphetamines using the Chiraldex™ G-PN column. Six baseline and nine partial separations were observed with the Lipodex™ D column, respectively.

A Critical View on the Quantification of Model Catalyst Activity

The conversion of reactants, reaction rate referred to catalyst mass, and turnover frequency (TOF) are values typically employed to compare the activity of different catalysts. However, experimental parameters have to be chosen carefully when systems of different complexity are compared. In order to characterize UHV-based model systems, we use a highly sensitive sniffer setup which allows us to investigate the catalytic activity by combining three different measurement modes: temperature-programmed desorption, continuous flow, and pulsed-reactivity experiments. In this article, we explore the caveats of quantifying catalytic activity in UHV on the well-studied and highly defined reference system of CO oxidation on Pt(111), which we later compare to the same reaction on Pt19 clusters deposited on Fe3O4(001). We demonstrate that we can apply fast heating ramps for TOF quantification, thus inducing as little sintering as possible in the metastable clusters. By changing the reactant ratio, we find transient reactivity effects that influence the TOF, which should be kept in mind when comparing catalysts. In addition, the TOF also depends on the surface coverage that itself is a function of temperature and pressure. At a constant reactant ratio, in the absence of transient effects, however, the TOF scales linearly with total pressure over the entire measured temperature range from 200 to 700 K since the reaction rate is dependent on both reactant partial pressures with temperature-dependent reaction order. When comparing the maximum TOF at this particular reactant ratio, we find a 1.6 times higher maximum TOF for Pt19/Fe3O4(001) than for Pt(111). In addition, pulsed-reactivity measurements help identify purely reaction-limited regimes and allow for a more detailed investigation of limiting reactants over the whole temperature range.

Thermo-mechanical waves in a biological tissue under ramp and oscillatory heat in Atangana–Baleanu fractional theory

Thermo-mechanical waves in a biological tissue under ramp and oscillatory heat in Atangana–Baleanu fractional theory

Pyrolysis of macroalgae: Insight into product yields and biochar morphology and stability

Pyrolysis of biomass residues into biochar is seen as a feasible way to mitigate climate change by biological carbon storage (carbon dioxide removal, CDR) and to substitute fossil fuel with sustainable biofuel. This study applies a combination of flash and ramp heating pyrolysis, and organic petrography to investigate the hydrocarbon (biofuel) potential and biochar stability and morphotypes of eight brown, red, and green macroalgal species of different tissue complexity. The carbon stability of biochar derived from macroalgae has not previously been assessed using organic petrography (reflectance measurements) and evaluated in the context of the geological carbon cycle. The biochar, hydrocarbon, and CO + CO2 yields vary due to different chemical composition of the macroalgal species, but the product yield variations are not related to the brown, red, or green macroalgal groups. The total biofuel yield shows an inverse trend with biochar yield. A slower heating rate produces more biochar and higher CO + CO2 and lower biofuel yields than the combined flash pyrolysis and faster heating rate. The morphotype composition of the biochar was qualitatively examined by reflected light microscopy while carbon stability was assessed by random reflectance (Ro) measurements. The diverse morphotype compositions observed in biochar formed under similar pyrolysis conditions likely stem from variations in the original algal composition. While some biochar samples show morphologies resembling the original macroalgal structure, porous morphotypes predominantly characterize the biochar samples overall. Despite a maximum pyrolysis production temperature (PT) of 650 °C, the highest mean Ro value among all biochar samples is 2.91%, corresponding to a carbonization temperature (CT) of 526 °C. This observation is tentatively related to the less lignocellulosic structure of the macroalgae compared to terrigenous biomass. Four biochar samples have their entire Ro distribution range above the inertinite benchmark (IBRo2%) of Ro = 2% indicating high carbon stability. Conversely, the remaining four biochar samples exhibit Ro distributions extending below IBRo2%, indicating the presence of a carbon fraction with lower long-term stability in soil. The statistically significant inverse relationship observed between the mean Ro values and the peak hydrocarbon generation temperature (Tmax) can be attributed to the behavior of residual macromolecules within the biochar. When these macromolecules reach peak biofuel generation at a lower temperature, they undergo carbonization over a more extended time interval during pyrolysis. Consequently, this prolonged exposure to the pyrolysis process leads to higher degrees of carbonization, as reflected by higher Ro values. In conclusion, the findings from pyrolysis and organic petrography reveal: (1) Macroalgae demonstrate potential for biofuel production, although biofuel yields contingent upon both the species of macroalgal and the heating rate employed, and (2) This study documents for the first time that flash+ramp pyrolysis of macroalgae yields biochar suitable for long-term carbon storage. However, both the carbon stability inferred from Ro frequency distributions and biochar yields show variations across different macroalgal species and heating rate.

Decoupled Crystallization and Particle Growth of BiVO4 via Rapid Thermal Process for Enhanced Charge Separation

AbstractBiVO4 is one of the most promising candidates for photoelectrochemical water oxidation. However, the poor crystallinity and short hole diffusion length limit its charge separation. One bottleneck stems from the contradiction between high crystallinity and small particles via conventional furnace heating processes. This paper describes the design and fabrication of BiVO4 photoanodes via rapid thermal process (RTP), rather than furnace heating, to decouple the constraints between nucleation, crystallization, and growth processes of BiVO4. The higher heating ramp rate of RTP compared with furnace heating promotes the fast diffusion of reactant molecules, which elevates the nucleation rate above the particle growth rate of BiVO4, leading to small particles with high crystallinity. Moreover, the ultra‐high heating temperature makes it possible to crystallize the small BiVO4 particle within a short time. Thus, a high crystallinity can be obtained for the RTP‐treated BiVO4 while maintaining small particle size, achieving a charge separation efficiency of up to 82%, 30% higher than that of furnace‐treated BiVO4 photoanode.

Effect of polyphenols from Ascophyllum nodosum seaweeds on the rheology and digestion of corn starch gels and gluten-free bread features

The main objective of this work is to study the effect of polyphenols, from the brown seaweed Ascophyllum nodosum, on the structure and digestion behaviour of gels at two corn starch concentrations (1.95 and 5.00% w/w) as well as the structure, color and texture features of crumbs from gluten-free breads. Adsorption isotherms of polyphenols on native and gelled starches were carried out and modelled by means of Langmuir and Henry models, respectively. The formation and characteristics of tested gels were rheologically monitored by means of heating ramp, time sweep at high temperature, cooling ramp and frequency sweep at 25 °C. Elastic modulus values decreased with the presence of polyphenols. Additionally, the polyphenols significantly decreased the digestion rate, measured by both chemical and rheological procedures, and the final concentration of digested starch. Finally, the presence of polyphenols in breads increased the hardness and chewiness values and decreased the cohesiveness and resilience values as well as the crumb hardening during storage.

Laser temperature programmed desorption: A flexible technique to study ion-surface interaction.

Understanding the physical-chemical processes ruling the interaction of particles (atoms, molecules, and ions) with surfaces is fundamental in several research fields, such as heterogeneous catalysis, astrochemistry, and nuclear fusion. In particular, the interaction of hydrogen isotopes with plasma facing materials represents a high-priority research task in the fusion community. Such studies are essential to ensure the successful operation of experimental fusion reactors, such as the tokamak ITER. In this work, we present a surface science apparatus developed to study ion-surface interaction in fusion relevant systems. It combines laser-based techniques with contaminant-free ion/molecular beams, mass spectrometry, and surface science tools such as low-energy electron diffraction and Auger electron spectroscopy. It allows to cover a wide range of sample temperatures, from 130 to 2300K, by changing the heating rate of samples from 0.1 to 135 K/s and maintaining the linearity of the heating ramps, a powerful feature to gain insight on adsorption, absorption, and desorption mechanisms. Experimental calibration and performance are presented in detail. Moreover, to provide a factual overview of the experimental capabilities, we focus on two different applications: the protocol used to clean a W(110) single crystal sample and the development of laser temperature programmed desorption to study helium retention in tungsten.

Self-extinguishable, intumescent poly(urethane-triazole)s as halogen-free flame retardant materials via bulk polymerization of azide-alkynes

In the present study, an unexplored class of non-halogenated self-extinguishable and intumescent phosphorous-based poly(urethane-triazole)s (P-PUTs) were achieved through the bulk polymerization of azide-alkynes notably in absence of catalyst. A series of azide-functionalized urethane monomers (tetra azides) were synthesized by the reaction of 1,3-diazido-propan-2-ol with commonly used, but three structurally different diisocyanates, viz, aliphatic, alicyclic, and aromatic. Concurrently, a dialkyne, phenyl di-prop-2-ynyl phosphonate was synthesized and co-polymerized with these urethane tetrazides through bulk polymerization at 80 °C. The curing kinetics of the polymerization was monitored by differential scanning calorimetry (DSC) under non-isothermal conditions with different heating ramps. Thermal behaviour, elemental and morphological properties of the synthesized P-PUTs were comprehensively investigated employing thermogravimetric analysis (TGA), field emission scanning electron microscopy (FE-SEM), and energy-dispersive X-ray spectroscopy (EDX), respectively. The flame retardant properties of P-PUTs were assessed by UL–94 vertical burning test, limiting oxygen index (LOI) and lab-scale flammability test. All the P-PUT compositions were found to self-extinguish immediately after the removal of flame with a V-0 rating of UL-94 V, the LOI value (vol%) are 26.3 %, 28.2 % and 29.0 % for H2P-PUT, I2P-PUT and T2P-PUT, respectively and the corresponding char yields were 26.03 wt%, 25.76 wt% and 39.58 wt% along with significant intumescence. This apart, the films with a transparency of 96.5 %, 96.7 % and 94.3 % in the visible wavelength for H2P-PUT, I2P-PUT and T2P-PUT, respectively, can possibly make these P-PUTs materials attractive as fire retardant top coats on wood substrates.

Soft Computing Model for Inverse Prediction of Surface Heat Flux from Temperature Responses in Short-Duration Heat Transfer Experiments

Abstract Aerodynamic experiments in high speed flow domain mainly rely on precise measurement transient surface temperatures and subsequent quantification of heat flux. These experiments are mainly simulated in high enthalpy short-duration facilities for which test flow duration are in the order of few milliseconds and the thermal loads resemble the nature of step/impulse. This study focuses on a specially designed fast-response coaxial surface junction thermal probe (CSTP) with capability of capturing transient temperature signals. The short-duration calibration experiments are realized to mimic the simulated flow conditions of high enthalpy test facilities. The classical one-dimensional heat conduction modelling has been used to deduce surface heat flux from the acquired temperature responses. It demonstrates a commendable accuracy of 2.5% when compared with known heat loads of calibration experiment. An advanced soft computing technique, the Adaptive Neuro-Fuzzy Inference System (ANFIS), is introduced for short-duration heat flux predictions. This methodology successfully recovers known (step or ramp) heat loads within a specific experimental time frame (0.2s). The results exhibit excellent agreement in prediction of trend and magnitude, carrying uncertainties of 3% for radiative and 5% for convective experiments. Consequently, the CSTP appears as a rapidly responsive transient heat flux sensor; for real-time short-duration experiments. The soft computing approach (ANFIS) offers an alternative means of heat flux estimation from temperature history irrespective of mode of heat transfer and nature of heat load, marked by its prediction accuracy, diminished mathematical intricacies, and reduced numerical requisites.