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Cyclohexanone–formaldehyde resin (CFR) was in situ modified with isocyanuric acid (ICA) in the presence of hydrochloric acid or p-toluenesulfonic acid by condensation polymerization. The purpose of this study is to produce isocyanuric acid-modified ketonic resins that have higher melting and decomposition temperature, and to use the produced resin in the production of fire-retardant polyurethane.

Two methods were used for in situ preparation of ICA-modified CFR in the presence of an acid catalyst. Method I: cyclohexanone, paraformaldehyde and ICA were mixed, and then an acid catalyst was added to form the modified CFR. Method II: ICA and formalin were mixed to produce N, N, N-trihydroxymethyl isocyanurate, and then water was removed under vacuum. The produced N, N, N-trihydroxymethyl isocyanurate solution was mixed with cyclohexanone and paraformaldehyde, then an acid catalyst was slowly added to this mixture to obtain ICA-modified CFR.

CFR was prepared in the presence of an acid catalyst. The product, CFR, has a dark red colour. The resulting resins have similar physical properties with the resin prepared in the presence of a basic catalyst. The solubility of ICA-modified CFR is much different than CFR in organic solvents.

This study focuses on obtaining an ICA-modified ketonic resin. Cyanuric acid has the form of an enolic structure under a basic condition; therefore, it cannot give a product with formaldehyde under basic conditions. The modification experiments were carried out in acidic conditions.

This study provides technical information for in situ modification of ketonic resin in the presence of acid catalysts. The resins may also promote the adhesive strength of the coating and provide corrosion inhibition on metal surfaces for a coating. The modified resins may also be used in the field of fire-retardant polyurethane applications.

These resins may be used for the preparation of non-toxic fire-retardant polyurethane foam. Polyurethane containing ICA-modified resin may exhibit better fire-retardant performance because of the incorporation of ICA molecule into the polyurethane structure.

ICA-modified CFRs have been synthesized in the presence of an acid catalyst, and the ICA-modified resin was used to produce fire-retardant polyurethane.

The purpose of this paper is to describe how lignosulphonate modified ketone formaldehyde resins containing functional groups such as hydroxyl, carbonyl, phenol, were produced via in situ modification of ketone/formaldehyde resins. Cyclohexanone‐formaldehyde (CF‐R), acetophenone‐formaldehyde (AF‐R) and methyl ethyl ketone‐formaldehyde (MEKFR) resins were in situ modified with lignosulphonate in the presence of sodium hydroxide. The paper reports the synthesis of lignosulphonate‐modified resins with a one step method of in situ modification of ketonic resin. The roles of the types of the ketone, lignosulphonate concentration, the solubility, molecular weight and thermal properties of the product were investigated.

Ketone, formalin (37 per cent aqueous solution), lignosulphonate were mixed and 20 per cent aqueous NaOH solution was added to produce the resin.

There was improvement of the properties of the lignosulphonate modified ketonic resins produced from waste black liquor. The lignosulphonate modified ketone‐formaldehyde resins were soluble in common organic solvents.

The reaction mixture must be stirred continuously. Subsequently, 37 per cent formalin was added dropwise in total while refluxing. The amount of aqueous NaOH solution is limited since the formed resin may become insoluble in common organic solvents. The water was removed from MEKFR, successively by evaporating with rotary evaporator.

This study provides the application of ketonic resins. The modified ketonic resins containing lignosulphonate groups may also promote the adhesive strength of a coating. The cell walls of various cell types of plants, for example, wood fibres, vessels, and tracheid, have lignin as an important constituent. It constitutes 20‐30 per cent of the weight of wood.

Lignosulphonate modified ketonic resins have been synthesized in the presence of a base catalyst. These resins have higher Tg or Tm values and molecular weight than CFR and AFR alone and also have thermoset property. Environmental and ecological concerns have increased the attention paid by the chemical industry to renewable raw materials.

This paper aims to investigate the prepared modified alkyd and poly(ester-amide) (PEA) resins as antimicrobial and insecticide binders for surface coating applications.

Salicylic diethanolamine and 4-(N, N-dimethylamino) benzylidene glutamic acid were prepared and used as new sources of polyol and dibasic acid for PEA and alkyd resins, then confirmed by: acid value, FT-IR and 1H-NMR. The coating performance of the resins was determined using measurements of physico-mechanical properties. The biological and insecticide activities of the prepared resins were investigated.

The tests carried out revealed that the modified PEA and alkyd enhanced both phyisco-mechanical and chemical properties in addition to the biological and insecticide activities. The results of this paper illustrate that the introduction of salicylic diethanolamine and 4-(N, N-dimethylamino) benzylidene glutamic acid within the resin structure improved the film performance and enhanced the antimicrobial activity performance of PEA and alkyd resins.

The modified alkyd and PEA organic resins can be used as biocidal binders when incorporated into paint formulations for multiple surface applications, especially those that are exposed to several organisms.

Modified alkyd and PEA resins based on newly synthesized modifiers have a significant potential to be promising in the production and development of antimicrobial and insecticide paints, allowing them to function to restrict the spread of insects and microbial infection.

The purpose of this paper is to report the synthesis of resins having conducting and fluorescence properties, with carbazole and oligocarbazole with a one step method of in situ modification of ketonic resin. Cyclohexanone‐formaldehyde (CFR), and acetophenone‐formaldehyde (AFR) resins were in situ modified with carbazole in the presence of sodium hydroxide.

Carbazole modified ketonic resins were synthesised by the condensation reaction of Cz, formaldehyde and ketone. Oligo carbazole was synthesised by redox reaction of carbazole and ceric ammonium nitrate (CAN). Then, for the in situ modification of oligo carbazole modified ketonic resin, reaction mixture of oligocarbazole carbazole was added to the cyclohexanone/formaldehyde solution.

The carbazole modified cyclohexanone‐formaldehyde and acetophenone formaldehyde resins have conductivity values of 10⁻⁵‐10⁻⁶ S/cm and may be considered as semi‐conductive ketonic resins. These new carbazole modified ketonic resins (CCzFR, ACzFR) have fluorescence properties.

This study focused on obtaining a conductive and fluorescence resin using a carbazole monomer which is an insulator.

This study provides technical information for the synthesis of fluorescence comonomer.

New CCzFR, ACzFR comonomers were synthesised. These comonomers have higher Tm values than CFR and AFR alone and also have fluorescence property.

The purpose of this paper is to investigate in situ modification of cyclohexanone‐formaldehyde resins (CFR) by 4‐vinyl aniline (Van). The roles of the reaction temperature, the conductivity, thermal properties, and molecular weight of the product were investigated. CFR was in situ modified with VAn in the presence of sodium hydroxide. Ketonic resin‐bound 4‐vinyl aniline was synthesised with a one‐step method of in situ modification of ketonic resin. The roles of the reaction temperature and the conductivity of the product were investigated.

Ketone, formalin (37% aqueous solution), vinyl aniline were mixed and then 20% aqueous NaOH solution was added to produce the resin. The solubility, molecular weight and thermal properties of the products were investigated.

The 4‐vinyl aniline modified cyclohexanone‐formaldehyde resins were found to have conductivity values of 10⁻⁴ and 10⁻² S/cm and may be considered as conductive ketonic resin. Soluble and processable conductive ketonic resins were developed.

The reaction mixture of CFR must be stirred continuously at low temperature. Subsequently, 37% formalin was added dropwise in equal portions while refluxing. Temperature should be controlled to prevent the thermal polymerisation of vinyl group and higher branching of amino groups. The amount of vinyl aniline used in reaction mixture is limited since the formed resin may become insoluble in common organic solvents.

This study provides technical information for the synthesis of conducting resins. The modified resins contain vinyl groups. The chemical redox or radical system can be used to polymerise these vinyl groups and resins with much higher molecular weight may be produced. The resins may also promote the adhesive strength of a coating and corrosion inhibition to metal surfaces of a coating.

Vinyl aniline modified cyclohexanone formaldehyde resins have been synthesised in the presence of a basice catalyst. These soluble and conductive resins may overcome difficulties in the applications of conducting polymers and open new application areas. Therefore, the vinyl aniline modified resin may find a number of new application areas, as well as existing conducting resin and polymer applications.

This paper aims to prepare a new modified poly(ester amide) (PEA) resins and use it as a binder for anticorrosive and antimicrobial coatings.

New modified PEA compositions were prepared based on 4-amino-N, N-bis(2-hydroxyethyl) benzamide (AHEB) as the ingredient source of the polyol used and evaluated as vehicles for surface coating. The structure of the modifier and PEA resin was confirmed by FT-IR, H¹-NMR, MW, thermogravimetric analysis and scanning electron microscope studies. Coatings of 50±5 µm thickness were applied to the surface of glass panels and mild steel strips by means of a brush. The coating performance of the resins was evaluated using international standard test methods and involved the measurement of phyisco-mechanical properties and chemical resistance.

The tests carried out revealed that the modified PEA based on AHEB enhanced both phyisco-mechanical and chemical properties. Also, the resins were incorporated within primer formulations and evaluated as anti-corrosive and antimicrobial single coatings. The results illustrate that the introduction of AHEB, within the resin structure, improved the film performance and enhances the corrosion resistance and antimicrobial activity performance of PEA resins.

The modified PEA compounds can be used as binders in paint formulations to improve the chemical, physical, corrosion resistance and antimicrobial activity properties.

Modified PEA resins are cheaper and can be used to replace other more expensive binders. These modified PEA resins can compensate successfully for the presence of many the anticorrosive and antimicrobial paint formulations, and thus, lower the costs. The main advantage of these binders is that they combine the properties of both polyester and polyamide resins based on nitrogenous compound, are of lower cost and they also overcome the disadvantages of both its counterparts. Also, they can be applied in other industrial applications.

Modifies short and medium alkyd resins using perfluori‐nated urethane toluene isocyanate (PFUTI), and incorporates the modified resins in a set of paint formulations containing different ratios of zinc phosphate as an inhibitive pigment. Achieves promising results and illustrates corrosion‐protective properties in various paint formulations and also a paint formulation free of the inhibitive pigment. Shows enhancement of the corrosion protection efficiencies by the improvement in the hydrophobicity of alkyd resin modified with PFUTI. In view of these results, minimizes or neglects the most expensive inhibitive pigments from an economical standpoint.

This paper aims to report the synthesis of resins having fluorescence properties, with the help of phenylacetylene (PhAc) by one-step method of in situ modification of ketonic resin. Cyclohexanone-formaldehyde resin (CFR) and acetophenone formaldehyde resin (AFR) were in situ modified with PhAc, in presence of sodium hydroxide (NaOH) by condensation polymerisation.

Ketone, formalin and phenylacetylene were mixed and then 20% aqueous NaOH solution was added to produce the phenylacethylene modified ketonic resin. The solubility, molecular weight and thermal properties of the products were investigated.

These new PhAc-modified ketonic resins (PAc-CFR and PAc-AFR) have fluorescence properties.

This study focuses on obtaining a fluorescence resin using a cyclohexanone, acetophenone and PhAc monomer which is an insulator.

This study provides technical information for the synthesis of fluorescence comonomers. The modified resins contain acetylene groups. A chemical redox or radical system can be used to polymerise these acetylene groups and resins with much higher molecular weight. The resins may also promote the adhesive strength of a coating and corrosion inhibition to metal surfaces of a coating.

The resins will be used for the preparation of AB- and ABA-type block copolymers. These block copolymers may exhibit different properties due to incorporation of monomer into the block copolymer structure.

PAc-CFR and PAc-AFR have been synthesised in the presence of a basic catalyst. Higher solubility and fluorescence intensity of the modified ketonic resins may increase their applications in the field of electroactive polymers and open new areas. These comonomers have fluorescence property.

To reduce the cost of epoxy adhesive without affecting the properties of epoxy adhesive in two pack system.

For effective toughening, adhesion, chemical resistance, etc. various compositions were made by incorporating flow modified solid epoxy resin. The impact, adhesive strengths and some other properties of the unmodified and modified epoxy networks were characterised.

The modification of epoxy resin using flow modified solid epoxy resin showed significant enhancement of impact and adhesive strengths and chemical resistance over the unmodified one. The optimum results were obtained at 13.66 parts per hundred parts of epoxy resin (phr) of modifier by replacing 4.33 phr of aerosil.

The modifier, 7004 FM, used in the present context was high molecular weight flow modified epoxy resin. Besides, these results could be obtained from other grades of flow modified high molecular weight epoxy resin. In addition, the efficiency of modification of epoxy resin using this could also be studied.

The method developed provided a simple and practical solution to removing the costly aerosil without affecting properties such as toughness, adhesive strength and chemical resistance of the cured epoxy.

The method for enhancing toughness, adhesive strength and chemical resistance of cured epoxy was novel and could find numerous applications in surface coating and adhesive.

Cyclohexanone‐formaldehyde resins (CF‐Rs) were in situ modified with aniline, 4‐aminodiphenylamine, and N‐N′‐diphenyl‐1,4‐phenylene diamine in presence of sodium hydroxide. The purpose of this paper is to report the synthesis of conducting resins with aniline, dimer and trimer aniline, with a one‐step method of in situ modification of ketonic resin. The roles of ketone, aniline concentration, the conductivity of the product are investigated.

Ketone, formalin (37 per cent aqueous solution), aniline or oligoaniline were mixed and 20 per cent aqueous NaOH solution was added to produce the resin.

The aniline‐modified (CF‐Rs) were found to have conductivity values of 10⁻³‐10⁻⁵ S/cm and may be considered as conductive ketonic resin.

The reaction mixture must be stirred continuously. Amount of aniline and oligoaniline is limited. Subsequently, 37 per cent formalin was added dropwise in total while refluxing. The amount of aniline is limited since the formed resin may become insoluble in common organic solvents.

This work provides the application of conducting resins. The modified resins containing aniline groups may also promote the adhesive strength of a coating and corrosion inhibition to metal surfaces.

Aniline formaldehyde, N‐N′‐diphenyl‐1,4‐phenylenediamine‐formaldehyde, aniline‐ and oligoaniline‐modified (CF‐Rs) have been synthesised in the presence of a base catalyst. These resins are conductive resins and the ketonic resins formed have physical properties of both aniline‐formaldehyde resins such as conductivity.