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Examines the fourteenth published year of the ITCRR. Runs the whole gamut of textile innovation, research and testing, some of which investigates hitherto untouched aspects. Subjects discussed include cotton fabric processing, asbestos substitutes, textile adjuncts to cardiovascular surgery, wet textile processes, hand evaluation, nanotechnology, thermoplastic composites, robotic ironing, protective clothing (agricultural and industrial), ecological aspects of fibre properties – to name but a few! There would appear to be no limit to the future potential for textile applications.

Gourd fibres (GF) are a natural biodegradable fibre material with excellent mechanical properties and high tensile strength. The use of natural fibres in composite materials has gained popularity in recent years due to their various advantages, including renewability, low cost, low density and biodegradability. Gourd fibre is one such natural fibre that has been identified as a potential reinforcement material for composites. However, it has low surface energy and hydrophobic nature, which makes it difficult to bond with matrix materials such as polyester. To overcome this problem, chemically adapted gourd fibre has been proposed as a solution. Chemical treatment is one of the most widely used methods to improve the properties of natural fibres. This research evaluates the feasibility and effectiveness of incorporating chemically adapted gourd fibre into polyester composites for industrial fabrication. The purpose of this study is to examine the application of chemically modified GF in the production of polyester composite engineering materials.

This work aims to evaluate the effectiveness of chemically adapted gourd fibre in improving the adhesion of gourd fibre with polyester resin in composite fabrication by varying the GF from 5 to 20 wt.%. The study involves the preparation of chemically treated gourd fibre through surface modification using sodium hydroxide (NaOH), permanganate (KMnO₄) and acetic acid (CH₃COOH) coupling agents. The mechanical properties of the modified fibre and composites were investigated. It was then characterized using scanning electron microscopy (SEM) and Fourier transform infrared spectroscopy (FTIR) to determine the changes in surface morphology and functional groups.

FTIR characterization showed that NaOH treatment caused cellulose depolymerization and caused a significant increase in the hydroxyl and carboxyl groups, showing improved surface functional groups; KMnO₄ treatment oxidized the fibre surface and caused the formation of surface oxide groups; and acetic acid treatment induced changes that primarily affected the ester and hydroxyl groups. SEM study showed that NaOH treatment changed the surface morphology of the gourd fibre, introduced voids and reduced hydrophilic tendencies. The tensile strength of the modified gourd fibres increased progressively as the concentration of the modification chemicals increased compared to the untreated fibres.

This work presents the designed composite with density, mechanical properties and microstructure, showing remarkable improvements in the engineering properties. An 181.5% improvement in tensile strength and a 56.63% increase in flexural strength were got over that of the unreinforced polyester. The findings from this work will contribute to the understanding of the potential of chemically adapted gourd fibre as a reinforcement material for composites and provide insights into the development of sustainable composite materials.

The paper discusses broadly electronic publishing and types of electronic publications. An attempt has been made to group the select electronic resources of chemical information into portals, patents and dissertations, full‐text files with backfiles and e‐books, abstracting and indexing services, encyclopaedias and handbooks, periodic tables, property databases and specialty databases. The paper concludes that in delivering electronic information two major developments are gaining momentum as archives from major publishers and preprints from academic circles are used as alternative methods of accessing research information. Also, scholarly publication of chemical information in electronic form will continue to grow, adapting to meet changing needs of authors and readers alike.

The aim of this paper is to conduct a real time evaluation of polypyrrole as an anti‐corrosive pigment in epoxy polyamide coating.

This study deals with synthesis of polypyrrole (PPy) by chemical oxidative polymerisation in laboratory conditions. The synthesised PPy was characterised by employing FT‐IR, XRD, SEM and EDX analysis. Epoxy film of bisphenol type hardened with polyamide based curing agent was used as the binder. PPy was used as anti‐corrosive pigment in concentrations varying from 0 to 5 wt% in the coating. In addition to anti‐corrosive property, mechanical, chemical and weathering properties of the coating containing PPy were studied and compared with epoxy polyamide coating without PPy.

The result obtained through various tests showed that the coating with 1 and 2% PPy exhibited excellent weathering resistance, mechanical properties and improved chemical resistance.

The anti‐corrosion property of the coating can be tested by means of atmospheric exposure such as Florida test or by means of electrochemical impedance spectroscopy.

The results find application in anti‐corrosive paints for industrial application.

This research paper presents the results of anti‐corrosion behaviour of PPy in epoxy‐polyamide coating. Based on this result, a highly effective anti‐corrosive coating can be formulated by addition of small percentage of PPy in combination with other conventional pigments, thereby enhancing corrosion protection.

Urethane Acrylate Oligomer with 100% solids was synthesised and characterised in order to study the application in electron beam curing with varying ratio of Trimethylol propane triacrylate (TMPTA). The purpose of this paper is to study effect of TMPTA addition on the crosslink density and different coating properties.

Polyester polyol was synthesised by reacting single diacid, adipic acid (AA), with Pentaerythritol (PENTA) and 1,6‐hexanediol (HD). Further, Urethane acrylate resin was synthesised by using Isophorone diisocyanate (IPDI), hydroxy ethyl acrylate (HEA) and Polyester polyol. The polyester polyol and urethane acrylate oligomer were characterised by 1H NMR, 13C NMR, FTIR and GPC. Further, TMPTA was added as a crosslinker to the urethane acrylate oligomer and cured by electron beam radiation. The cured UA films having varying concentration of TMPTA were employed to evaluate thermal property, contact angle analysis, mechanical and chemical properties.

The obtained results showed improvement in their chemical properties, mechanical properties, thermal properties and water contact angle at 20% of TMPTA iconcentration. The TMPTA also reduced the dose required for the curing.

The resin can be synthesised from different isocyanates as TDI, MDI and HMDI, etc. The study can also be done with different multi or mono functional monomers such as methacrylate, hexanediol diacrylate, ethylene glycol diacrylate, etc.

The paper provides the better solution to reduce the cost of the electron beam radiation required for the curing.

The method presented in the paper could be very useful for controlling environmental pollution; as the conventional method of curing releases volatile organic compounds (VOC).

In this paper, urethane acrylate and TMTPA cured with electron beam are shown to offer good coating properties. A high‐solid urethane acrylate coating would find numerous industrial applications in surface coatings.

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.

The paper's aim is to synthesise ultraviolet (UV) curable polyurethane acrylate based on polyester polyol and to study change in its mechanical, chemical, optical and weather resistance properties with varying amount of nanosilica. It also seeks to determine its optimum loading levels for property maximisation.

New UV curable polyurethane acrylate has been synthesised using polyester polyol, blend of isophorone diisocyanate and toluene diisocyanate and hydroxyl ethyl acrylate. This resin was incorporated with nanosilica (1‐3 per cent) on the basis of total solids. The newly synthesised material was characterised by fourier transform infrared spectroscopy, gel permeation chromatography, X‐ray diffraction and scanning electron microscopy. The mechanical, chemical and optical properties of the coating films were studied and compared.

The hardness, tensile strength and abrasion resistance show significant enhancement with increasing amount of nanosilica. It is also found that UV cured polyurethane acrylate nanocoating exhibited improved weather resistance. The optimum concentration of nanosilica for better performance is found to be 3 per cent of total solids. The improvement is the result of inherent nature of nanosilica.

Nanosilica used in present context is having 10 nm mean diameter and near about 600 m²/g surface area. Nanosilica having different particle size, surface area and surface modification can be used to improve more specific properties.

Addition of nanosilica particles to polyurethane acrylate coating is a simple and inexpensive method resulting in phenomenal increase in properties.

The new organic‐inorganic hybrid nanocoating with improved weather resistance was synthesised. These coatings could find applications in demanding fields such as automotive topcoats.

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.

The purpose of this paper is to explore the application of triglycidyl resin (TGC) prepared from cardanol as partial replacement of conventional bis-phenol A (BPA) based epoxy resin for zinc rich primers (ZRPs).

The synthesis of new platform chemicals that are based on renewable resources has been accepted as a strategy to contribute to sustainable development due to the anticipated depletion of fossil oil reserves and rising oil prices. We prepared a tri-functional epoxy resin from cardanol which can be used as partial replacement of BPA based epoxy. The ZRPs were prepared using 50:50 ratio of TGC:BPA epoxy, and the coatings were evaluated for mechanical, chemical and anticorrosive properties.

The 50 per cent replacement of BPA based epoxy by TGC resulted in at par mechanical, chemical and anticorrosive properties as evaluated by various methods. The successful implementation can thus contribute to sustainable development by “green chemistry” route.

The prepared TGC resin in the current work was studied for application in ZRPs. This can also be explored for high performance coatings, adhesives and other engineering applications.

The TGC binder was prepared by simple two-step reaction. This can successfully be used as binder for coating application without any modifications.

A novel approach of using green and ecofriendly TGC resin as replacement of high cost BPA based epoxy was explored and can be implemented for numerous applications.

Solutions of the twin plane jets HF chemical laser flow based on a turbulent kinetic theory, due to a modified Green’s function method, are presented. The calculated results of probability density function (PDF) of various chemical species in velocity space, and mass fraction concentration distributions of various reactants and products in the flow field, are revealed and discussed in this analysis. The transport phenomena of different pumping rate, collisional deactivation rate, and radiative deactivation rate in the interaction between the twin plane jets HF chemical laser show that the properties of species mass fraction concentrations, collisional reaction rate, and radiative incident intensity are the dominant factors. The present study provides the fundamentals for theoretical understanding of twin plane jets HF chemical laser and further application to multiple‐jet HF chemical laser analysis.