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Novel bleach activator compounds derived from the reaction of isocyanic acid with selected nucleophiles / David M. Lewis in COLORATION TECHNOLOGY, Vol. 139, N° 4 (08/2023)
[article]
Titre : Novel bleach activator compounds derived from the reaction of isocyanic acid with selected nucleophiles Type de document : texte imprimé Auteurs : David M. Lewis, Auteur ; Jamie A. Hawkes, Auteur Année de publication : 2023 Article en page(s) : p. 355-368 Note générale : Bibliogr. Langues : Anglais (eng) Catégories : Agents de blanchiment
Chimie textile
Composés organiques -- Synthèse
Détergents
Textiles et tissusIndex. décimale : 668.1 Agents tensioactifs : savons, détergents Résumé : Laundry detergents commonly contain bleach activators that react with the perhydroxy anion produced from perborate or percarbonate anions to form activated peroxy compounds; these enhance bleaching and stain removal capacity especially at lower temperatures, hydrogen peroxide being an inefficient bleach below 60°C. The most commonly used activators are N, N, N′, N′-tetraacetylethylenediamine (TAED) and sodium nonanoyloxybenzenesulphonate (SNOBS) the former being used across Europe whereas the latter is used widely in the United States and Japan. This research studies the preparation of novel activator compounds which are carbamylated derivatives of selected nucleophiles using either solid or aqueous reactions of nucleophilic carboxylate anions with the highly reactive isocyanic acid entity derived from the acidification of sodium cyanate. The novel activator compounds were then assessed as bleach activators by testing against tea and bilberry-stained cotton reference fabrics at 40°C in the presence of hydrogen peroxide at pH values ranging from 4 to 10; bleaching efficiency was assessed visually and colorimetrically. Results showed that all of the synthesised compounds were more effective bleach activators across the pH range tested than the standard TAED system. Note de contenu : - EXPERIMENTAL : Materials - Methods
- RESULTS AND DISCUSSION : Synthesis of sodil amino(oxo) methanesulphonate "monomer" (SAMS-M) - Synthesis of sodio amino(oxo) methanesulphonate "allophonate" (SAMS-A) - Synthesis of 4-[(aminocarbonyl)oxy]benzenesulphonic acid “monomer” (ACOBS-M) - Synthesis of 4-[(aminocarbonyl)oxy]benzenesulphonic acid “allophonate” (ACOBS-A) - Synthesis of benzoate-O-carbamate (BOCM) - Synthesis of citrate-O-(carboxy) carbamate (COCM) - Activated bleach testing
- Table 1 : Percentage reduction in colour (% Red) after treatment with bleaching solutions
- Table 2 : Conditions used to evaluate varying SAMS-A/hydrogen peroxide concentrations
- Table 3 : Percentage reduction in colour (% Red) after treatment with SAMS-A bleaching solutionsDOI : https://doi.org/10.1111/cote.12662 En ligne : https://onlinelibrary.wiley.com/doi/epdf/10.1111/cote.12662 Format de la ressource électronique : Permalink : https://e-campus.itech.fr/pmb/opac_css/index.php?lvl=notice_display&id=39675
in COLORATION TECHNOLOGY > Vol. 139, N° 4 (08/2023) . - p. 355-368[article]Réservation
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Code-barres Cote Support Localisation Section Disponibilité 24152 - Périodique Bibliothèque principale Documentaires Disponible The reaction of sodium cyanate with wool and nylon and its effect on subsequent dyeing / David Lewis in COLORATION TECHNOLOGY, Vol. 130, N° 2 (04/2014)
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Titre : The reaction of sodium cyanate with wool and nylon and its effect on subsequent dyeing Type de document : texte imprimé Auteurs : David Lewis, Auteur ; Jamie A. Hawkes, Auteur ; Yong Lu, Auteur Année de publication : 2014 Article en page(s) : p. 127-132 Note générale : Bibliogr. Langues : Anglais (eng) Catégories : Carbamoylation
Carboxylate
Chimie textile
Cyanate de sodium
Isocyanates
Laine
Polyamide 66
Teinture -- Fibres textilesIndex. décimale : 667.3 Teinture et impression des tissus Résumé : This paper describes the reaction of the simplest isocyanate, isocyanic acid, conveniently generated in situ from sodium cyanate, with nucleophilic carboxylate and amino residues in polyamide fibres. Changing the pH conditions greatly affects the outcome of these reactions: under acidic conditions the carboxylate residues are selectively carbamoylated, whereas under neutral conditions both residues are carbamoylated. Such modifications greatly change the dyeing behaviour of the treated substrates. The carboxylate carbamoylation reaction leads to the formation of amides rather than the carbamoylcarboxylate, which is a reactive intermediate. DOI : 10.1111/cote.12072 En ligne : https://onlinelibrary.wiley.com/doi/epdf/10.1111/cote.12072 Format de la ressource électronique : Permalink : https://e-campus.itech.fr/pmb/opac_css/index.php?lvl=notice_display&id=20868
in COLORATION TECHNOLOGY > Vol. 130, N° 2 (04/2014) . - p. 127-132[article]Réservation
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Code-barres Cote Support Localisation Section Disponibilité 16129 - Périodique Bibliothèque principale Documentaires Disponible