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Synthesis, characterization, and UV curing of acrylate functional hyperbranched polyester resins / Mats Johansson in JOURNAL OF COATINGS TECHNOLOGY (JCT), Vol. 67, N° 849 (10/1995)
[article]
Titre : Synthesis, characterization, and UV curing of acrylate functional hyperbranched polyester resins Type de document : texte imprimé Auteurs : Mats Johansson, Auteur ; Anders Hult, Auteur Année de publication : 1995 Article en page(s) : p. 35-39 Note générale : Bibliogr. Langues : Américain (ame) Catégories : Caractérisation
Couches minces
Dureté (matériaux)
Liants
Polyacrylates
Polyesters
Polymères aliphatiques
Polymères ramifiés
Résistance chimique
Réticulation (polymérisation)
Revêtements
Revêtements -- Propriétés mécaniques:Peinture -- Propriétés mécaniquesIndex. décimale : 667.9 Revêtements et enduits Résumé : A series of different hyperbranched aliphatic polyester resins with acrylate functionality have been synthesized, characterized, and UV cured. The terminal groups have been either benzoates, propionates, or hydroxyls. The glass transition (Tg) and viscosity of the resins have been shown to depend on the polarity of the end groups. The increase in viscosity gives the hydroxy functional resin the highest viscosity, while the propionate functional resin has the lowest Tg and viscosity. The acrylates are all free radically UV cured with little or no oxygen inhibition found. The residual unsaturation in the cured films is not detectable with Raman spectroscopy, i.e., less than five percent. The cured films are all hard with a Tg difference varying with the structure of terminal groups in the resins. Note de contenu : - EXPERIMENTAL : Materials - Technique - Synthesis - Rheology - Curing of the acrylate resins - Film properties
- RESULTS AND DISCUSSION : Synthesis and chemical characterization - Rheology - Curing of the acrylate resins - Film propertiesPermalink : https://e-campus.itech.fr/pmb/opac_css/index.php?lvl=notice_display&id=18561
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Code-barres Cote Support Localisation Section Disponibilité 003495 - Périodique Bibliothèque principale Documentaires Disponible 003507 - Périodique Bibliothèque principale Documentaires Exclu du prêt Synthesis of castor oil/2,4-toluene diisocyanate adduct to impart water repellency and antibacterial properties for cotton/polyester fabric / H. M. Fahmy in JOURNAL OF COATINGS TECHNOLOGY AND RESEARCH, Vol. 16, N° 1 (01/2019)
[article]
Titre : Synthesis of castor oil/2,4-toluene diisocyanate adduct to impart water repellency and antibacterial properties for cotton/polyester fabric Type de document : texte imprimé Auteurs : H. M. Fahmy, Auteur ; A. Amr, Auteur ; A. A. Aly, Auteur ; Sh. M. Sayed, Auteur Année de publication : 2019 Article en page(s) : p. 31-39 Note générale : Bibliogr. Langues : Américain (ame) Catégories : Additifs
Antibactériens
Composés organiques -- Synthèse
CotonLe coton est une fibre végétale qui entoure les graines des cotonniers "véritables"(Gossypium sp.), un arbuste de la famille des Malvacées. Cette fibre est généralement transformée en fil qui est tissé pour fabriquer des tissus. Le coton est la plus importante des fibres naturelles produites dans le monde. Depuis le XIXe siècle, il constitue, grâce aux progrès de l'industrialisation et de l'agronomie, la première fibre textile du monde (près de la moitié de la consommation mondiale de fibres textiles).
Diisocyanate de toluèneLe diisocyanate de toluène (TDI : Toluene diisocyanate) est un composé organique, toxique et allergène, appartenant au groupe des isocyanates.
C'est l'un des monomères de départ utilisés pour la production de polyuréthane par polymérisation.
Le TDI peut réagir avec un polyol ce qui permet de former une structure uréthane.
Le TDI est produit industriellement en faisant réagir du diaminotoluène (en fait un mélange de 2,4-diaminotoluène et de 2,6-diaminotoluène dans un ratio 80:20) avec du phosgène (COCl2), ce qui conduit au TDI avec une production secondaire de chlorure d'hydrogène HCl.
Il sert à fabriquer des mousses expansées, molles, semi-rigides ou rigides de polyuréthane, des adhésifs, peintures, enduits souples, élastomères, etc.
Emulsions
Huile de ricin et constituants
Imperméabilisation
Matériaux -- Propriétés fonctionnelles
Polyesters
Polyuréthanes
Textiles et tissusIndex. décimale : 667.9 Revêtements et enduits Résumé : A new CAO/TDI adduct was synthesized by reacting 2,4-toluene diisocyanate (TDI) with castor oil (CAO) in a molar ratio of 70%, respectively, at 100°C for 90 min. The chemical structure of the synthesized adduct was confirmed by FTIR analysis. Furthermore, such adduct was emulsified in water using stearic acid/triethanol amine system. Moreover, the emulsion was examined as a water-repellent as well as an antibacterial finish for cotton/polyester fabric. The results indicated that the emulsion treated fabric acquires water repellency, softness, stiffness, and antibacterial properties. In addition, the surface of the aforementioned treated fabric was characterized via scanning electron microscopy. Note de contenu : - METHODS : Synthesis of CAO/TDI adduct - Purification of CAO/TDI adduct - Emulsification of CAO/TDI adduct
- FACTORS AFFECTING THE CAO/TDI ADDUCT SYNTHESIS : Reaction time and temperature - TDI/CAO molar ratio
- FTIR ANALYSIS OF THE PURIFIED CAO/TDI ADDUCT
- FACTORS AFFECTING EMULSIFICATION OF THE CAO/TDI ADDUCT IN WATER : Stearic acid concentration - Degree of neutralization of SA with TEA - Type of deactivating metal salt - AlCl3/SA molar ratio
- FACTORS AFFECTING APPLICATION OF THE CAO/TDI ADDUCT AS WATER-REPELLENT FINISH : Adduct concentration
- Table 1 : Effect of SA concentration on the emulsion state and water repellency rating of treated fabric
- Table 2 : Effect of adduct concentration on the emulsion state and water repellency rating of treated fabric
- Table 3 : Some performance and functional properties of the CAO/TDI adduct emulsion treated fabricDOI : 10.1007/s11998-018-0097-9 En ligne : https://link.springer.com/article/10.1007/s11998-018-0097-9 Format de la ressource électronique : Permalink : https://e-campus.itech.fr/pmb/opac_css/index.php?lvl=notice_display&id=31962
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Code-barres Cote Support Localisation Section Disponibilité 20659 - Périodique Bibliothèque principale Documentaires Disponible Synthesis of a curing agent containing trifunctional epoxy groups for powder coatings and its curing reaction kinetics / Qiuping Su in JOURNAL OF COATINGS TECHNOLOGY AND RESEARCH, Vol. 19, N° 3 (05/2022)
[article]
Titre : Synthesis of a curing agent containing trifunctional epoxy groups for powder coatings and its curing reaction kinetics Type de document : texte imprimé Auteurs : Qiuping Su, Auteur ; Zilun Tang, Auteur ; Jiajian He, Auteur ; Yuxin Gu, Auteur ; Yong Li, Auteur ; Jing Xie, Auteur ; Shaoshun Wang, Auteur ; Ruijun Lin, Auteur ; Xiaofeng Lin, Auteur ; Wenjing Lin, Auteur ; Guobin Yi, Auteur Année de publication : 2022 Article en page(s) : p. 907-917 Note générale : Bibliogr. Langues : Américain (ame) Catégories : Caractérisation
Cinétique chimique
Composés organiques -- Synthèse
Morphologie (matériaux)
Polyesters
Polymérisation
Réticulants
Revêtements organiques
Revêtements poudre
Stabilité thermiqueIndex. décimale : 667.9 Revêtements et enduits Résumé : In this work, tris(oxiran-2-ylmethyl) benzene-1,3,5-tricarboxylate (TOTC) was synthesized by a new two-step method without using harmful epichlorohydrin and served as a curing agent for polyester powder coatings. The chemical structure of TOTC was determined by Fourier transform infrared spectroscopy and nuclear magnetic resonance spectroscopy. The curing behavior and the curing reaction kinetics of TOTC/polyester resin (NH-3307) system were studied by dynamic differential scanning calorimetry. The activation energy Ea was 71.75 kJ mol-1 according to Flynn–Wall–Ozawa method, and the curing reaction of TOTC/NH-3307 system was described by Friedman method. It was found that the curing reaction of TOTC/NH-3307 system was a two-parameter autocatalysis which followed the Šestάk–Berggren model. The nonisothermal curing reaction rate was simulated according to the Šestάk–Berggren model and the experimentally parameters. What is more, the thermogravimetric analysis results showed that the TOTC/NH-3307 system had good thermal stability with an initial decomposition temperature of 374.92°C. The TOTC/NH-3307 cured film exhibited excellent leveling performance by SEM. The results demonstrated that TOTC has efficient curing ability and huge market potential. Note de contenu : - Experimental : Materials
- Methods : Synthesis of triallyl benzene-1,3,5-tricarboxylate (TATC)
- Synthesis of tris(oxiran-2-ylmethyl) benzene-1,3,5-tricarboxylate (TOTC)
- Preparation of powder coatings
- Characterization and instrumentation
- Results and discussion : Synthesis and characterization of TOTC
- Curing kinetics and mechanism analysis : Nonisothermal DSC cure
- Curing kinetics
- Curing mechanism
- Thermal stability analysis
- Surface morphology analysis
- Table 1 : Characteristic parameters of TOTC/NH-3307 powder coating system
- Table 2 : Characteristic peak conversion values and calculated kinetic parameters for autocatalytic model at different heating ratesDOI : https://doi.org/10.1007/s11998-021-00578-7 En ligne : https://link.springer.com/content/pdf/10.1007/s11998-021-00578-7.pdf Format de la ressource électronique : Permalink : https://e-campus.itech.fr/pmb/opac_css/index.php?lvl=notice_display&id=38085
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Code-barres Cote Support Localisation Section Disponibilité 23605 - Périodique Bibliothèque principale Documentaires Disponible Synthesis of a novel hyperbranched polyester with carboxyl end groups applied to UV-curable waterborne coating / Jieming Liu in JOURNAL OF COATINGS TECHNOLOGY AND RESEARCH, Vol. 18, N° 1 (01/2021)
[article]
Titre : Synthesis of a novel hyperbranched polyester with carboxyl end groups applied to UV-curable waterborne coating Type de document : texte imprimé Auteurs : Jieming Liu, Auteur ; Shaoshun Wang, Auteur ; Qiuping Su, Auteur ; Jiajian He, Auteur ; Yong Li, Auteur ; Jing Xie, Auteur ; Guobin Yi, Auteur Année de publication : 2021 Article en page(s) : p. 259-269 Note générale : Bibliogr. Langues : Américain (ame) Catégories : Analyse mécanique dynamique
Caractérisation
Groupement carboxyle
Hydrostabilité
Polyesters
Polymères -- Synthèse
Polymères ramifiés
Revêtements -- Propriétés mécaniques
Revêtements -- Propriétés thermiques
Revêtements en phase aqueuse
Revêtements en phase aqueuse -- Séchage sous rayonnement ultraviolet
Revêtements organiques
Rhéologie
SolubilitéIndex. décimale : 667.9 Revêtements et enduits Résumé : A hyperbranched polyester with carboxyl end group (HPC) was synthesized by using trimellitic anhydride and neopentyl glycol as raw materials via A2 + B3 polycondensation. Then, waterborne hyperbranched polyester acrylate (WHPC) was synthesized by partially modifying the carboxylic groups of HPC with glycidyl methacrylate. In order to explore the influence of molecular weight, acrylate groups content, and ion groups content on performances, a series of WHPC films with different molecular weight, acrylate groups content, and ion groups content were prepared. The dynamic light scattering spectrometer analysis shows that the higher ionic groups content and the lower molecular weight cause the smaller particle size. The ionic group content has a positive effect on the solubility. The smaller molecular weight and particle size cause the lower viscosity. The Fourier-transform IR spectrophotometer reveals that the double bond final conversion increased with increasing acrylate groups content. The final conversion is between 69 and 86%. The curing speed is fast, and the curing time is about 70 s due to the numerous end groups owned by the hyperbranched structure. The dynamic mechanical thermal analysis coupled with end-use mechanical property tests illustrates that the crosslink density has a positive effect on the storage modulus and a negative effect on the flexibility. It is also found that glass transition temperature and pencil hardness are determined by the balance between crosslink segment and hyperbranched polyester segment. The thermogravimetric analysis proves that increased crosslink density and molecular weight promote the heat resistance of films. This work utilizes a novel hyperbranched structure that excels in viscosity, flexibility, and water solubility. Furthermore, the preparation process is convenient. Note de contenu : - EXPERIMENTAL : Materials - Synthesis of hyperbranched polyester with carboxyl end groups (HPC) - Synthesis of waterborne hyperbranched polyester acrylate (WHPC) - Neutralization of the prepolymer - Dispersion formation - UV curing - Measurements
- RESULTS AND DISCUSSION : Characterizations of hyperbranched polyester - Gel permeable chromatography (GPC) analysis - Particle size - Rheological behavior - Water solubility and stability - Curing kinetics and boule bond conversion - Dynamic mechanical thermal analysis (DMTA) - Thermal properties
- Table 1 : Sample designation and stoichiometric ration of -COO- and GMA for the preparation of WHPC
- Table 2 : The particle diameter in water and COO- groups content of WHPCs
- Table 3 : Dynamic mechanical properties of the UV-cured coatings
- Table 4 : The mechanical properties and performance of the UV-cured coatings
- Table 5 : The degradation temperature at 5% weight lossDOI : https://doi.org/10.1007/s11998-020-00404-6 En ligne : https://link.springer.com/content/pdf/10.1007/s11998-020-00404-6.pdf Format de la ressource électronique : Permalink : https://e-campus.itech.fr/pmb/opac_css/index.php?lvl=notice_display&id=35368
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Code-barres Cote Support Localisation Section Disponibilité 22605 - Périodique Bibliothèque principale Documentaires Disponible Synthesis of UV-curable polyesters with lateral double bonds by ring-opening polymerization and their properties / Yumei Zhou in JOURNAL OF COATINGS TECHNOLOGY AND RESEARCH, Vol. 18, N° 6 (11/2021)
[article]
Titre : Synthesis of UV-curable polyesters with lateral double bonds by ring-opening polymerization and their properties Type de document : texte imprimé Auteurs : Yumei Zhou, Auteur ; Shujie Ming, Auteur ; Liuyan Tang, Auteur ; Jinqing Qu, Auteur Année de publication : 2021 Article en page(s) : p. 1591-1601 Note générale : Bibliogr. Langues : Américain (ame) Catégories : Anhydrides
Caractérisation
Catalyseurs
Copolymère vinyle ester
Copolymérisation
Epoxydes
Monomères
Oligomères
Photoréticulation
Polyesters
Revêtements -- Séchage sous rayonnement ultraviolet
Revêtements organiques
Stabilité thermique
ViscositéIndex. décimale : 667.9 Revêtements et enduits Résumé : UV-curable coatings have been receiving more and more attention for their high performance and environmentally friendly advantages, which meet the “5 E” requirements of coating development. Vinyl oligomer is the main factor affecting the performance of UV-curable coating, but it is difficult to meet the requirements of high-end UV curing technology due to its high viscosity, low vinyl functionality, and high cost. Herein, polyesters with lateral double bonds were prepared by ring-opening polymerization of acid anhydride and glycidyl methacrylate. The epoxy compound without vinyl groups was used to participate in the polymerization reaction to adjust the viscosity and vinyl functionality of the resin. Furthermore, the molecular structure and molecular weight of the polyesters were characterized by FTIR, 1H NMR, and GPC. The effects of the categories and proportions of acid anhydride and glycidyl ether on the viscosity and hardness of the coating films were studied. The results indicated that the use of acid anhydrides containing phenyl rigid groups could significantly increase the hardness of the paint film, and the long-chain tertiary glycidyl carbonate (E10P) had the best viscosity reduction effect. When the molar ratio of acid anhydride, GMA and E10P was 4:1:3, the viscosity of the prepared vinyl polyester was low to 2755 mPa·s. In this case, the hardness of the paint film was as high as H, and it also exhibited excellent water resistance and alcohol resistance. Note de contenu : - EXPERIMENTAL : Materials - Preparation of UV-curable polyesters with lateral double bonds - Characterization
- RESULTS AND DISCUSSION : Influencing factors of polyester performances - Structural characterization of the polyesters - Analysis of photocuring behavior of the polyesters - Thermal stability of the polyesters - Film properties of the polyesters
- Table 1 : Effect of glycidyl methacrylate content on the properties of the polyesters
- Table 2 : Effect of anhydride type on the properties of the polyesters
- Table 3 : Effect of different epoxy monomers on the properties of the polyesters
- Table 4 : Copolymerization of PA and epoxides
- Table 5 : Selection of different ring-opening catalysts
- Table 6 : GPC results of the polyesters
- Table 7 : The film properties of the polyesterDOI : https://doi.org/10.1007/s11998-021-00513-w En ligne : https://link.springer.com/content/pdf/10.1007/s11998-021-00513-w.pdf Format de la ressource électronique : Permalink : https://e-campus.itech.fr/pmb/opac_css/index.php?lvl=notice_display&id=36818
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PermalinkUtilisation des colles adhésifs et peintures dans la construction et l'entretien des bateaux de plaisance / Association Française des Techniciens des Peintures, Vernis, Encres et Adhésifs / Paris : AFTPVA (1995)
PermalinkUV curing polymers in leather finishing / M. A. Knight in JOURNAL OF THE SOCIETY OF LEATHER TECHNOLOGISTS & CHEMISTS (JSLTC), Vol. 62, N° 1 (01-02/1978)
PermalinkUV curing polymers in leather finishing / M. A. Knight in JOURNAL OF THE SOCIETY OF LEATHER TECHNOLOGISTS & CHEMISTS (JSLTC), Vol. 61 et 62 (Années 1977 et 1978)
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PermalinkWater-dispersible hot melt adhesive formulations / Richard A. Miller in ADHESIVES AGE, Vol. 40, N° 12 (11/1997)
PermalinkWater dispersible hot melt adhesive raw material / Richard A. Miller in ADHESIVES AGE, Vol. 38, N° 13 (12/1995)
PermalinkWater-dispersible raw materials for adhesives / Richard A. Miller in ADHESIVE TECHNOLOGY, Vol. 15, N° 3 (09/1998)
PermalinkWater-dispersible raw materials for hot melt adhesives / Richard A. Miller in ADHESIVES AGE, Vol. 39, N° 12 (11/1996)
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