Accueil
Détail de l'indexation
667.3 : Teinture et impression des tissus 667.1 Nettoyage
667.2 Colorants et pigments 667.4 Encres 667.5 Encres d'imprimerie 667.6 Peintures 667.7 Cires, laques, vernis 667.9 Revêtements et enduits |
Ouvrages de la bibliothèque en indexation 667.3
Ajouter le résultat dans votre panier Affiner la recherche
3-Hydroxy-2-[1'-phenyl-3'-(p-chlorophenyl)-4'-pyrazolyl]-4-oxo-4H-1-benzopyran as a spectrophotometric reagent for trace determination of tungsten(vi) / R. Agnihotri in COLORATION TECHNOLOGY, Vol. 124, N° 6 (2008)
[article]
Titre : 3-Hydroxy-2-[1'-phenyl-3'-(p-chlorophenyl)-4'-pyrazolyl]-4-oxo-4H-1-benzopyran as a spectrophotometric reagent for trace determination of tungsten(vi) Type de document : texte imprimé Auteurs : R. Agnihotri, Auteur ; R. Kamal, Auteur ; N. Agnihotri, Auteur ; J. R. Mehta, Auteur Année de publication : 2009 Article en page(s) : p. 379-384 Note générale : Bibliogr. Langues : Anglais (eng) Index. décimale : 667.3 Teinture et impression des tissus Résumé : 3-Hydroxy-2-[1'-phenyl-3'-(p-chlorophenyl)-4'-pyrazolyl]-4-oxo-4H-1-benzopyran solution in acetone forms a yellow-coloured complex with tungsten(vi) in perchloric acid medium which is extractable into chloroform after equilibration. In this study, tests were carried out on this compound and it was found to be quite stable and to obey Beer's law. Interactions with various ions were studied and the molar absorptivity, Sandell's sensitivity and relative standard deviation were also investigated. Job's method, the mole ratio method and the equilibrium-shift method were also used. The ratio of metal to ligand was measured using a method that was simpler, more accurate, sensitive, rapid and selective as compared with existing methods. This method is applicable to the analysis of various samples of varied composition. DOI : 10.1111/j.1478-4408.2008.00167.x En ligne : http://onlinelibrary.wiley.com/doi/10.1111/j.1478-4408.2008.00167.x/pdf Format de la ressource électronique : Permalink : https://e-campus.itech.fr/pmb/opac_css/index.php?lvl=notice_display&id=3248
in COLORATION TECHNOLOGY > Vol. 124, N° 6 (2008) . - p. 379-384[article]Réservation
Réserver ce document
Exemplaires (1)
Code-barres Cote Support Localisation Section Disponibilité 010992 - Périodique Bibliothèque principale Documentaires Disponible 4,5-Dinitrosulfonefluorescein and related dyes : Kinetics of reversible rupture of the pyran ring and their interaction with lysozyme / Nika N. Kriklya in COLORATION TECHNOLOGY, Vol. 137, N° 6 (12/2021)
[article]
Titre : 4,5-Dinitrosulfonefluorescein and related dyes : Kinetics of reversible rupture of the pyran ring and their interaction with lysozyme Type de document : texte imprimé Auteurs : Nika N. Kriklya, Auteur ; Taras Yu. Gromovoy, Auteur ; Nicolay O. Mchedlov-Petrossyan, Auteur Année de publication : 2021 Article en page(s) : p. 658-667 Note générale : Bibliogr. Langues : Anglais (eng) Catégories : Caractérisation
Colorants -- Analyse
Dynamique moléculaire
Fluorescence
LysozymeLe lysozyme est une protéine globulaire formée de 129 acides aminés (chez l'être humain), que l'on rencontre dans un certain nombre de sécrétions (larmes, salive, lait maternel, mucus...) et dans le blanc d'œuf, chez de nombreuses espèces d'animaux, dont insectes et acariens1.
Il s'agit d'une hydrolase acide (EC 3.2.1.17) sécrétée par les granulocytes et les monocytes. Elle détruit la paroi bactérienne en catalysant l'hydrolyse des peptidoglycanes la constituant.
Spectrométrie de masseIndex. décimale : 667.3 Teinture et impression des tissus Résumé : Fluorescein and sulfonefluorescein dyes are stable in solution within a wide pH range. Nucleophilic addition of the hydroxide (HO–) group to the nodal carbon atom is not typical of these compounds. They are also not prone to rupture of the pyran cycle under the action of alkali. However, the last-named heterocycle readily opens at high pH values in the case of derivatives containing nitro groups in the xanthene moiety. Moreover, while in the case of nitrofluoresceins, for example, 4,5-dinitrofluorescein, this reaction is irreversible, with 4,5-dinitrosulfonefluorescein acidification of the alkaline solution immediately returns the visible absorption spectrum to that of the original hydroxyxanthene dye. We present a quantitative study of the kinetics of the pyran cycle rupture in aqueous alkali without and with micelles of a cationic surfactant. Also, both initial dye and reaction product were studied via the matrix-assisted laser desorption/ionisation time-of-flight (MALDI-ToF) technique. The second part of the article is devoted to the interaction of 4,5-dinitrosulfonefluorescein and other dyes of similar structure with lysozyme basing on the MALDI-ToF mass spectrometry. This made it possible to arrange the dyes according to their affinity for the protein and draw some conclusions about the nature of the association of the dye with lysozyme. Note de contenu : - EXPERIMENTAL : Materials - Mass spectrometry - Characterisation of the colloidal species - Procedure of the kinetics study
- RESULTS AND DISCUSSION : Alkaline rupture of the pyrancycle of 4,5-dinitrosulfonefluorescein - Kinetic data processing : Aqueous NaOH solutions - Surfactant effect : 4,5-dinitrosulfonefluorescein in the aqueous CTAB/NaOH system - The behaviour of 2,4,5,7-tetranitrosulfonefluorescein in alkaline aqueous media - Interaction of the dyes with lysozymeDOI : https://doi.org/10.1111/cote.12565 En ligne : https://onlinelibrary.wiley.com/doi/epdf/10.1111/cote.12565 Format de la ressource électronique : Permalink : https://e-campus.itech.fr/pmb/opac_css/index.php?lvl=notice_display&id=36795
in COLORATION TECHNOLOGY > Vol. 137, N° 6 (12/2021) . - p. 658-667[article]Réservation
Réserver ce document
Exemplaires (1)
Code-barres Cote Support Localisation Section Disponibilité 23068 - Périodique Bibliothèque principale Documentaires Disponible 6-pyridinium benzo[a]phenazine-5-oxide derivatives as visible photosensitisers for polymerisation / Karolina Podemska in COLORATION TECHNOLOGY, Vol. 130, N° 4 (08/2014)
[article]
Titre : 6-pyridinium benzo[a]phenazine-5-oxide derivatives as visible photosensitisers for polymerisation Type de document : texte imprimé Auteurs : Karolina Podemska, Auteur ; Radoslaw Podsiadly, Auteur ; Agnieszka Orzel, Auteur ; Anna Kowalska, Auteur ; Andrzej Marcinek, Auteur ; Jolanta Sokolowska, Auteur Année de publication : 2014 Article en page(s) : p. 250-259 Note générale : Bibliogr. Langues : Anglais (eng) Catégories : Colorants -- Synthèse
Décoloration
Photo-oxydation
Photoamorceurs (chimie)
Photochimie
Polyaddition
Triacrylate de triméthylolpropaneIndex. décimale : 667.3 Teinture et impression des tissus Résumé : Several 6-pyridinium benzo[a]phenazine-5-oxide derivatives have been synthesised and characterised by proton nuclear magnetic resonance spectroscopy and mass spectrometry. The spectroscopic and electrochemical properties of these dyes were examined. The dyes were used as reducible sensitisers for selected electron donors (phenylthioacetic acid, phenoxyacetic acid, N-phenylglycine, and ethyl 4-N,N-dimethylaminobenzoate) and as oxidisable sensitisers for electron acceptors (onium and N-alkoxypyridinium salts). These photoredox pairs were found to be effective visible-wavelength photoinitiators for the free radical polymerisation of trimethylolpropane triacrylate under visible light. The cationic photopolymerisation of cyclohexene oxide by the studied dyes and the onium salt photoredox pairs was ineffective. The obtained results are discussed on the basis of both free energy change for electron transfer to or from the benzo[a]phenazine dyes and the photochemical properties of the dyes, particularly their photobleaching. The proposed mechanism of dye fading is supported by density functional theory calculations and spectroscopic characterisation of the radical cation of the dye. Note de contenu : - Synthesis of 6-pyridinium benzo[a]phenzzine-5-oxide (2a)
- Quantum chemical calculations
- Photochemical experimentsDOI : 10.1111/cote.12096 En ligne : https://onlinelibrary.wiley.com/doi/epdf/10.1111/cote.12096 Format de la ressource électronique : Permalink : https://e-campus.itech.fr/pmb/opac_css/index.php?lvl=notice_display&id=21776
in COLORATION TECHNOLOGY > Vol. 130, N° 4 (08/2014) . - p. 250-259[article]Réservation
Réserver ce document
Exemplaires (1)
Code-barres Cote Support Localisation Section Disponibilité 16443 - Périodique Bibliothèque principale Documentaires Disponible Absorption of nanoparticles by wool / David G. King in COLORATION TECHNOLOGY, Vol. 125, N° 2 (2009)
[article]
Titre : Absorption of nanoparticles by wool Type de document : texte imprimé Auteurs : David G. King, Auteur ; Anthony P. Pierlot, Auteur Année de publication : 2009 Article en page(s) : p. 111-116 Note générale : Bibliogr. Langues : Anglais (eng) Index. décimale : 667.3 Teinture et impression des tissus Résumé : Wool was treated with inorganic and polymer-based nanoparticles. The diffusion of nanoparticles into wool appears to be dependent on electrostatic interactions. In particular, it is optimised at low pH in which there are very few anionic groups on the wool fibre; the nanoparticles also need to have sufficient charge to maintain their stability as dispersion. The findings support the view that the cell membrane complex and other low sulphur regions are the main route of entry for both molecular and macromolecular treatment chemicals. The use of this technique to treat wool may lead to new coloration effects and other functions such as antimicrobial action. DOI : 10.1111/j.1478-4408.2009.00182.x En ligne : http://onlinelibrary.wiley.com/doi/10.1111/j.1478-4408.2009.00182.x/pdf Format de la ressource électronique : Permalink : https://e-campus.itech.fr/pmb/opac_css/index.php?lvl=notice_display&id=4856
in COLORATION TECHNOLOGY > Vol. 125, N° 2 (2009) . - p. 111-116[article]Réservation
Réserver ce document
Exemplaires (1)
Code-barres Cote Support Localisation Section Disponibilité 011226 - Périodique Bibliothèque principale Documentaires Disponible Acrylic/keratin composite of enhanced dyeability towards cationic and anionic dyes / Lamiaa El-Gabry in COLORATION TECHNOLOGY, Vol. 132, N° 1 (02/2016)
[article]
Titre : Acrylic/keratin composite of enhanced dyeability towards cationic and anionic dyes Type de document : texte imprimé Auteurs : Lamiaa El-Gabry, Auteur ; Amira Abou El-Kheir, Auteur Année de publication : 2016 Article en page(s) : p. 83-91 Note générale : Bibliogr. Langues : Anglais (eng) Catégories : Colorants acides
Colorants cationiques
Colorants réactifs
Couches minces
Déchets industriels -- Recyclage
Dissolution (chimie)
kératinesLa kératine est une protéine, synthétisée et utilisée par de nombreux êtres vivants comme élément de structure, et également l'exemple-type de protéine fibreuse.
La kératine est insoluble, et peut être retrouvée sur l'épiderme de certains animaux, notamment les mammifères, ce qui leur garantit une peau imperméable. Parfois, lors d'une friction trop importante, la kératine se développe à la surface de la peau formant une callosité. Les cellules qui produisent la kératine meurent et sont remplacées continuellement. Les morceaux de kératine qui restent emprisonnés dans les cheveux sont couramment appelés des pellicules.
La molécule de kératine est hélicoïdale et fibreuse, elle s'enroule autour d'autres molécules de kératine pour former des filaments intermédiaires. Ces protéines contiennent un haut taux d'acides aminés à base de soufre, principalement la cystéine, qui forment un pont disulfure entre les molécules, conférant sa rigidité à l'ensemble. La chevelure humaine est constituée à 14 % de cystéine.
Il y a deux principales formes de kératines : l'alpha-kératine, ou α-keratin, présente chez les mammifères notamment, dont l'humain, et la bêta-kératine, ou β-keratin, que l'on retrouve chez les reptiles et les oiseaux. Ces deux types de kératines ne présentent clairement pas d'homologie de séquence.
Chez l'être humain, la kératine est fabriquée par les kératinocytes, cellules se trouvant dans la couche profonde de l'épiderme. Les kératinocytes absorbent la mélanine (pigment fabriqué par les mélanocytes), se colorent et ainsi cette pigmentation de l'épiderme permet de protéger les kératinocytes des rayons ultraviolets du Soleil. (Wikipedia)
Polyacryliques
Poudres
Teinture -- Fibres textilesIndex. décimale : 667.3 Teinture et impression des tissus Résumé : Acrylic and keratin industrial wastes were dissolved, each separately, in their respective proper solvents. The soluble keratin was regenerated into powder and then mixed with the soluble acrylic to form an acrylic/keratin composite that was finally cast into film. The topography of the acrylic/keratin film was studied using scanning electron microscopy. The chemical composition of the obtained film was assigned using elemental analysis and infrared spectroscopy. The substantivity of the prepared acrylic/keratin film towards anionic (acid and reactive) and cationic (basic) dyes was studied. The obtained film exhibited high dyeability towards both acid and reactive dyes even at relatively low dyeing temperatures. Hydrazine hydrate was used to enhance the dyeability of the said film with acid and reactive dyes. Kinetic studies of the dyeing of the film with anionic dyes were also conducted. Note de contenu : - EXPERIMENTAL : Materials - Chemicals - Dyestuff - Method - Dyeing process - Analysis and testing
- RESULTS AND DISCUSSION : Surface morphology - Dyeing - Kinetic study - Infrared spectroscopy - Elemental analysisDOI : 10.1111/cote.12190 Permalink : https://e-campus.itech.fr/pmb/opac_css/index.php?lvl=notice_display&id=25579
in COLORATION TECHNOLOGY > Vol. 132, N° 1 (02/2016) . - p. 83-91[article]Réservation
Réserver ce document
Exemplaires (1)
Code-barres Cote Support Localisation Section Disponibilité 17865 - Périodique Bibliothèque principale Documentaires Disponible Acryloyl esters of emodin for waterless dyeing and toxicological studies / Gabriel Rampazzo Magalhães in COLORATION TECHNOLOGY, Vol. 140, N° 4 (08/2024)
PermalinkAdsorption and fixation behaviour of CI Reactive Red 195 on cotton woven fabric in a nonionic surfactant Triton X-100 reverse micelle / Shixiong Yi in COLORATION TECHNOLOGY, Vol. 128, N° 4 (2012)
PermalinkAdsorption behaviour of azo disperse dyes on polyurethane fibre / Hong-Fei Qian in COLORATION TECHNOLOGY, Vol. 125, N° 3 (2009)
PermalinkAdsorption behaviour of carbon black/latex by cationised cotton fabrics / Chunxia Wang in COLORATION TECHNOLOGY, Vol. 131, N° 6 (12/2015)
PermalinkAdsorption characteristics of CI Basic Blue 3 from aqueous solution onto Aleppo pine-tree sawdust / Naima Ouazene in COLORATION TECHNOLOGY, Vol. 128, N° 1 (2012)
PermalinkAdsorption characteristics of ionic and nonionic surfactants on hydrophobic pigment in aqueous medium / Hikmet Sis in COLORATION TECHNOLOGY, Vol. 128, N° 3 (2012)
PermalinkAdsorption equilibrium studies of a simulated textile effluent containing a wool reactive dye on gallinaceous feathers / Olga M. Freitas in COLORATION TECHNOLOGY, Vol. 132, N° 5 (10/2016)
PermalinkAdsorption of basic dyes from model aqueous solutions onto novel spherical silica support / Teofil Jesionowski in COLORATION TECHNOLOGY, Vol. 124, N° 3 (2008)
PermalinkAdsorption of a spent reactive dyebath by a chitosan bed : study of water reuse, bed regeneration, and UV/Fenton oxidation / Chunhui Li in COLORATION TECHNOLOGY, Vol. 130, N° 2 (04/2014)
PermalinkAdsorption removal of Brilliant green and Safranin-O contaminants from water using a hydrogel based on carboxymethyl cellulose and sodium alginate crosslinked by epichlorohydrin / Khushbu in COLORATION TECHNOLOGY, Vol. 139, N° 4 (08/2023)
PermalinkAdsorption studies on the treatment of textile dyeing effluent by activated carbon prepared from olive stone by ZnCl2 activation / Mehmet Ugurlu in COLORATION TECHNOLOGY, Vol. 123, N° 2 (2007)
PermalinkAfterclearing of disperse dyed polyester with gaseous ozone / Hüseyin Aksel Eren in COLORATION TECHNOLOGY, Vol. 128, N° 2 (2012)
PermalinkAldehyde-functionalised distyrylbenzene : Photophysical properties and primary amine sensitivity evaluation in solution and solid state / Fateme Sadat Miri in COLORATION TECHNOLOGY, Vol. 138, N° 6 (12/2022)
PermalinkAlizarin old and new : Extraction techniques for coloration, advances in detection methods for historical textiles and novel applications as a functional dye / Khai Ly Do in COLORATION TECHNOLOGY, Vol. 140, N° 1 (02/2024)
PermalinkAlkali dissolution behaviour of sea–island-type polyethylene terephthalate ultramicrofibre knitted fabrics / Hyun Sung Kim in COLORATION TECHNOLOGY, Vol. 130, N° 5 (10/2014)
Permalink