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The purpose of this paper is to evaluate the fire resistance of an innovative carbon-reinforced PEKK composite for aeronautical applications. To this end, thermal degradation analysis under inert and oxidative atmosphere is carried out. Moreover, a linear model fitting approach is compared to a generally used isoconversional method to validate its reliability for kinetic triplet estimation.

Thermogravimetric analysis carried out under inert and oxidative atmospheres, between 25 and 1000°C for three different heating rates (5, 15, 25°C/min), followed by a qualitative SEM observation of the samples before and after thermal treatment. After the reaction identification by TG/DTG curves, an isoconversional analysis is carried out to estimate the activation energy as a function of the reaction conversion rate. For the identified reactions, the kinetic triplet is estimated by different methods and the results are compared to evaluate their reliability.

In inert case, one global reaction, observed between 500-700°C, seems able to describe the degradation of carbon-PEKK resin. Under oxidative atmosphere, three main reactions are identified, besides the resin degradation, the other two are attributed to char and fiber oxidation. Good agreement achieved between isoconversional and linear model fitting methods in activation energy calculation. The achieved results demonstrate the high thermal resistance of PEKK associated with the ether and ketone bonds between the three aromatic groups of its monomer.

This paper provides a possible degradation model useful for numerical implementation in CFD calculations for aircraft components design, when exposed to high temperatures and fire conditions.

The purpose of this paper is to study thermal stability, curing kinetics and physico‐chemical properties of polyurethanes systems for application in in‐mould decoration (IMD) ink.

The thermal stability of three Polyurethane (Pu) systems A, B, C were evaluated by thermogravimetric analysis (TGA). The kinetic parameters of the curing reaction of Pu system C were calculated using non‐isothermal curing kinetics analysis, including the activation energy Ea, the reaction rate constant K(T), the reaction order n, the initial curing temperature (Ti), the peak temperature (Tp), and the finishing temperature (Tf). Additionally, physico‐chemical properties were also evaluated such as flexibility, impact resistance, pencil hardness, adhesive attraction and solvent resistance.

TGA showed that thermal decomposition temperature T5 (5 wt.% weight loss), T10 (10 wt.% weight loss) and Tend (decomposition termination temperature) of Pu system C was 344°C, 363°C, and 489°C, respectively. T5, T10, Tend increased by 77°C, 61°C, 4°C, respectively, and the char yield at 600°C increased by 25.1 wt.% comparing with Pu system B. Curing kinetics analysis showed that Ea of Pu system C was 62.29 KJ/mol, 65.98 KJ/mol and 65.95 KJ/mol by Kissinger, Flynn‐Wall‐Ozawa and Ozawa method, respectively. The order of the curing reaction (n=0.90) demonstrated that it was a complex reaction. Moreover, Pu system C exhibited good physico‐chemical properties. The results showed that Pu system C was suitable to apply into IMD ink.

The TGA analysis, curing kinetics analysis and evaluation of physico‐chemical properties provided a simple and practical solution to study suitable resins for IMD ink application.

IMD ink for heat transfer printing technology is highly efficient, relatively low cost, clean and environmentally safe. It has been widely applied into medical and pharmaceutical products, electronic devices, telecommunication equipment, computer parts, appliance panels, automotive parts, etc.

In this paper, the thermal stability and curing kinetics of Pu for IMD ink are reported for the first time. The paper gives very interesting and important information about thermal stability, curing kinetics and properties of Pu coating system for IMD ink application.

In order to study its cure response and to understand its kinetic behaviour, this paper seeks to examine how a multifunctional epoxy resin, N,4‐bis(4‐(bis(2‐oxiranylmethyl)amino)‐2‐chlorobenzyl)‐3‐chloro‐N‐(2‐oxiranylmethyl)benzenamine (BCCOMB), synthesised from amine functional chloroaniline formaldehyde condensate (AFCFC) and epichlorohydrine, is cured with AFCFC as curing agent.

For effective curing, AFCFC (12.5 phr, part per 100 resin) was added to BCCOMB resin and mixed thoroughly for 15 minutes. The clear viscous solution was then subjected to DSC analyses for kinetics study of the curing reaction.

The AFCFC was successfully utilised as curing agents for BCCOMB as the DSC curves show complete curing exotherm. The presence of oxirane group in the BCCOMB was able to react with active hydrogen atoms of amine. This led to conversion of liquid monomers of thermoset resin into three‐dimensional network.

In the present discussion, the curing study of BCCOMB had been done using AFCFC as a curing agent. However, other curing agents, synthesised from other amine and aldehyde, could also be used to see whether they would be effective for curing study of BCCOMB.

The method for curing study of multifunctional epoxy resin (BCCOMB) was novel and the cured epoxy network could find numerous applications as surface coating and adhesive on to an intricate structure.

The silicone modifications of two-component epoxy resin coatings are commonly built on epoxy resins rather than on epoxy curing agents. The silicone-modified epoxy curing agent system is rarely reported yet. This study aims to prepare the polysiloxane (PS)-modified waterborne epoxy coatings based on aqueous curing agents technology.

Waterborne epoxy curing agents with different contents of terminal epoxy PS were synthesized by reacting with triethylenetetramine, followed by incorporating of epoxy resin (NPEL-128) and polyethylene glycol diglycidyl ether. The waterborne epoxy coatings were prepared with the above curing agents, and their performance was investigated through thermogravimetric analysis, scanning electron microscopy, mechanical characterization, gloss measurement, chemical resistance test and ultraviolet (UV) aging experiment.

The results showed that the epoxy coating prepared by silicon-modified curing agent has higher gloss, better chemical resistance and UV resistance than the coating from unmodified curing agent with terminal epoxy PS and commercially available waterborne epoxy curing agent (Aradur 3986), as well as the competitive mechanical properties and heat resistance. Reduced water absorption on fibrous paper was also obtained with the help of silicon-modified curing agent.

These findings will be valuable for resin researchers in addressing the modification issues about waterborne epoxy resin and curing agent.

Reliable modeling of induction hardening requires a multi-physical approach, which makes it time-consuming. In designing an induction hardening system, combining such model with an optimization technique allows managing a high number of design variables. However, this could lead to a tremendous overall computational cost. This paper aims to reduce the computational time of an optimal design problem by making use of multi-fidelity modeling and parallel computing.

In the multi-fidelity framework, the “high-fidelity” model couples the electromagnetic, thermal and metallurgical fields. It predicts the phase transformations during both the heating and cooling stages. The “low-fidelity” model is instead limited to the heating step. Its inaccuracy is counterbalanced by its cheapness, which makes it suitable for exploring the design space in optimization. Then, the use of co-Kriging allows merging information from different fidelity models and predicting good design candidates. Field evaluations of both models occur in parallel.

In the design of an induction heating system, the synergy between the “high-fidelity” and “low-fidelity” model, together with use of surrogates and parallel computing could reduce up to one order of magnitude the overall computational cost.

On one hand, multi-physical modeling of induction hardening implies a better understanding of the process, resulting in further potential process improvements. On the other hand, the optimization technique could be applied to many other computationally intensive real-life problems.

This paper highlights how parallel multi-fidelity optimization could be used in designing an induction hardening system.

The purpose of this paper is to evaluate the efficiency of acrylated guar gum (AGG) as an additive in alkyd resin for improved mechanical properties and to optimize the results of such an addition.

For studying the effect of AGG on coating properties, guar gum was modified to various degrees of esterification and various compositions of alkyd systems were made by incorporating different concentrations of AGG. The mechanical and solvent absorption of the unmodified and modified alkyd systems were characterized.

The incorporation of AGG into alkyd coating showed significant improvement of mechanical properties over the unmodified one. The modification caused an additional crosslink site through its unsaturation which led to increased crosslink density without phase separation of additive from the alkyd system which was confirmed by SEM scans.

The reactive additive, AGG used in the present study was synthesised using acryloyl chloride. Besides, it could also be synthesised from methacryloyl chloride and the effect of methyl substitution on water and solvent absorption could be studied.

The method developed provided a simple and practical solution to improving the mechanical properties of alkyd coatings.

The method for enhancing mechanical properties of cured alkyd system was novel and could find numerous applications in surface coatings.

The purpose of this study is to synthesize structurally different phenalkamines based on cardanol, a renewable material obtained from cashew nut shell liquid, and to evaluate their effect on performance properties of the coatings.

For this purpose, the Mannich reaction between cardanol, formaldehyde and various diamines such as diaminodiphenyl methane (DDM), hexamethylene diamine, Jeffamine D400 and Jeffamine T403 were carried out to produce novel phenalkamines. Resultant phenalkamines were used as curing agents for commercial DGEBPA epoxy resin and were evaluated for performance properties.

The mechanical, optical, chemical, thermal and anticorrosive properties were evaluated and compared with those of commercial phenalkamine AG141. It was observed that anticorrosive properties evaluated using a salt spray test and electrochemical impedance spectroscopy revealed significant improvement in anticorrosive performance of coatings cured with synthesized phenalkamines based on DDM and T403 as compared to the coatings based on commercial phenalkamine AG141.

To obtain optimum performance properties of the coatings, a combination of phenalkamines can be used.

Curing time and gel times of all the phenalkamines can be further studied under wet and humid conditions. In addition, the variation in coating properties under humid conditions can be investigated.

In this study, newer phenalkamines were synthesized and used as curing agents for epoxy coatings. So far, there have been no reports indicating the synthesis and application of phenalkamines based on polyetheramines, namely, Jeffamine D400 and Jeffamine T403, in coating applications.

This paper aims to deal with the experimental and numerical investigations of the fire protection performance of a waterborne intumescent coating (IC) on structural steel in case of natural fires. Based on own small-scale laboratory tests, an advanced numerical model is developed to simulate the fire protection performance of the investigated coating in case of arbitrary fire scenarios. The insulation efficiency of the coating is described within the model by temperature and heating rate-dependent material properties, such as expansion factors, thermal conductivity and heat capacity. The results of the numerical model are compared to own large-scale fire tests of an unloaded I-section beam and column.

As natural fires can show arbitrary regimes, the material properties of the waterborne IC are investigated for various heating rates. Based on these investigations, a material model for the IC is implemented in the finite element program ABAQUS. With the help of user subroutines, the material properties of the coating are introduced for both the heating and cooling phase of natural fires, allowing for two- and three-dimensional thermomechanical analyses of coated steel elements.

The results of the performed small-scale laboratory tests show a heating rate-dependent behavior of the investigated coating. The mass loss as well as the expansion of the coating change with the heating rate. Moreover, the material properties obtained on small scale are valid for large scale. Therefore, a material model could be developed that is suitable to reproduce the results of the large-scale fire tests. Additionally, with the help of the numerical model, a dimensioning approach for the dry film thickness (DFT) of the investigated coating is derived for arbitrary natural fires.

The material properties presented in this paper are only valid for the investigated waterborne IC and the parameter area that was chosen. However, the developed modeling approach for the fire protection performance of ICs is general and can be applied for every coating that is part of the intumescent product family.

Until now, only few research works have been carried out on the fire protection performance of ICs under non-standard fire exposure. This paper deals extensively with the material properties and the material modeling of a waterborne IC exposed to natural fires. Especially, the laboratory examinations and the numerical simulations are unique and allow for new evaluation possibilities of ICs.