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Aliphatic epoxy emulsion crosslinker for waterborne coatings / Delano R. Eslinger in JOURNAL OF COATINGS TECHNOLOGY (JCT), Vol. 67, N° 850 (11/1995)
[article]
Titre : Aliphatic epoxy emulsion crosslinker for waterborne coatings Type de document : texte imprimé Auteurs : Delano R. Eslinger, Auteur Année de publication : 1995 Article en page(s) : p.45-50 Note générale : Bibliogr. Langues : Américain (ame) Catégories : Epoxydes
Formulation (Génie chimique)
Groupement carboxyle
Polyacryliques
Réticulants
Revêtements en phase aqueuse:Peinture en phase aqueuseIndex. décimale : 667.9 Revêtements et enduits Résumé : Many waterborne polymers and dispersions have carboxyl functionality in their structure. These carboxyl groups are multifaceted in their utility. They are often necessary to introduce water solubility or water dispersibility characteristics to waterborne resins, impart stability to waterborne vahicles, and often offer advantages in dried film properties, especially with respect to substrate adhesion. However, due to the hydrophilic nature of these carboxyl groups, fims from waterborne coatings often exhibit high water vapor permeability and poor wet adhesion properties. Note de contenu : - Epoxy crosslinkers
- Nature of the carboxylic group
- Acrylic emulsions and dispersions
- Epoxy index
- Evaluation of commercially available acrylic emulsions
- Effect of catalyst
- Pot life considerations
- Formaldehyde free baking enamelsPermalink : https://e-campus.itech.fr/pmb/opac_css/index.php?lvl=notice_display&id=18577
in JOURNAL OF COATINGS TECHNOLOGY (JCT) > Vol. 67, N° 850 (11/1995) . - p.45-50[article]Réservation
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Code-barres Cote Support Localisation Section Disponibilité 003496 - Périodique Bibliothèque principale Documentaires Disponible 003508 - Périodique Bibliothèque principale Documentaires Exclu du prêt Application of carboxyl-functionalized epoxy resin in the leather tanning process / Bin Lyu in JOURNAL OF THE AMERICAN LEATHER CHEMISTS ASSOCIATION (JALCA), Vol. CXIII, N° 7 (07/2018)
[article]
Titre : Application of carboxyl-functionalized epoxy resin in the leather tanning process Type de document : texte imprimé Auteurs : Bin Lyu, Auteur ; Li Yajuan, Auteur ; Dangge Gao, Auteur ; Jianzhong Ma, Auteur ; Lv Leihong, Auteur Année de publication : 2018 Article en page(s) : p. 225-231 Note générale : Bibliogr. Langues : Américain (ame) Catégories : Cuir -- Teneur en chrome hexavalent
Cuirs et peaux -- Propriétés mécaniques
Cuirs et peaux -- Propriétés physiques
Détérioration enzymatique
Douceur (toucher)
Eaux usées -- Teneur en chrome hexavalent
Epoxydes
Groupement carboxyle
Polymères -- Synthèse
Réactions chimiques
Stabilité hydrothermale
Tannage
Température de retraitIndex. décimale : 675.2 Préparation du cuir naturel. Tannage Résumé : Chrome tanning is widely used in the tanning process ; however, it can cause environmental pollution. Leather tanned with epoxy resin was considered as a more environmentally friendlyprocess, but it takes as long as five days for reaction, and results in poor performance of leather. The aim of the present study was to tan leather collagen with a carboxyl-functionalized epoxy resin, which was thought to be an eco-friendly tanning process and the reaction time was shortened to 12h. The reaction between carboxyl-functionalized epoxy resin and leather collagen can be divided into two stages, the reaction of epoxy group with leather collagen and the reaction of carboxyl group with leather collagen. The influences of tanning conditions (medium pH, epoxy resin amount and reaction time) on the properties of tanned leather were also discussed. In the first stage, the epoxy group was reacted with leather collagen in basic conditions. The results showed that the carboxyl-functionalized epoxy resin could better penetrate into the leather fibers when the pH value was 8.5, and the best effect of tanned leather collagen was found using reaction condition of pH 7.0. In the second stage, it was the reaction of carboxyl group to leather collagen in acid conditions, and the best effect was found under the condition of pH was 3.5. Meanwhile, it provided a better tanning effect when the carboxyl-functionalized epoxy resin amount was 6% and the reaction time was 12h. The chrome-less tanning process that carboxyl-functionalized epoxy resin combination with 3% chrome was studied. The results showed that the hydrothermal stability and strength properties of leather tanned by carboxyl-functionalized epoxy resin with 3% chrome were close, even superior, to those of the leather produced by conventional chrome tanning with 8% chrome. Note de contenu : - MATERIALS AND METHODS :
- Material
- Methods : Synthesis of the carboxyl-functionalized epoxy resin - Tanning methodology
- Testing and characterization : Shrinkage temperature - Thickness increment ratio - Mechanical properties - Softness - Enzymatic degradation - Chrome content in leather and waste water - Calculation
- RESULTS :
- Tanning conditions of carboxyl-functionalized epoxy resin pH : The amount of tanning agent
- Chrome-less tanning results : SEM topography of the leather - Physical properties - Mechanical properties - Softness - Enzymatic degradation - Chrome content in leather and waste waterEn ligne : https://drive.google.com/file/d/1zAn7Cgd6nhD2xonUrhpGkK5uE09EybTG/view?usp=drive [...] Format de la ressource électronique : Permalink : https://e-campus.itech.fr/pmb/opac_css/index.php?lvl=notice_display&id=30830
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Code-barres Cote Support Localisation Section Disponibilité 20080 - Périodique Bibliothèque principale Documentaires Disponible Balancing adhesion and cohesion in WB packaging adhesives / Bradley A. Jacobs in ADHESIVES AGE, Vol. 39, N° 12 (11/1996)
[article]
Titre : Balancing adhesion and cohesion in WB packaging adhesives Type de document : texte imprimé Auteurs : Bradley A. Jacobs, Auteur Année de publication : 1996 Article en page(s) : p. 40-44 Note générale : Bibliogr. Langues : Américain (ame) Catégories : Adhésifs en phase aqueuse
Adhésion
Copolymère acrylique acétate de vinyle
Groupement carboxyle
Pelage
Polyacétate de vinyle
Résistance à l'arrachement
Résistance au cisaillement
Résistance au fluage
Réticulation (polymérisation)
ThermogravimétrieIndex. décimale : 668.3 Adhésifs et produits semblables Résumé : Challenges posed by low energy substrates, environmental regulations, product integrity and economic pressure place demands on adhesive performance that are increasingly difficult to meet using traditional technologies. PVOH-stabilized vinyl acetate/acrylics present a new approach to satisfying these demands. While VAAs have found initial acceptance in applications requiring Tgs below the range accessible with VAE technology, this work has demonstrated that VAAs offer advantages even at higher Tgs. Rovace HP-3442 exhibits an attractive combination of adhesion to a wide range of difficult-to-bond substrates, cohesive strength comparable to VAEs and good creep resistance. The scope of this study has been the performance of the copolymer backbones, but other advantages of using VAAs become apparent when compounding begins. PVOH stabilization gives the VAAs excellent mechanical stability and compatibility with common formulating raw materials. The incorporation of carboxyl functionality provides reactive groups for crosslinking chemistry. And the vinyl acrylic copolymers are compatible with a range of tackifiers and other additives that provide added versatility and flexibility for formulating to meet specific performance requirements (3). Couple these benefits with the economics of vinyl acetate copolymers and one can see low VAAS are the-state-of-the-art in waterborne adhesive emulsions. Note de contenu : - ADHESION VS.COHESION
- EXPERIMENTAL : Quantitative adhesive strength - Quantitative cohesive strength - 180° peel adhesion - Hot shear strength - Thermogravimetric analysis (TGA)
- RESULTS AND DISCUSSION : Peel adhesion - Shear adhesionEn ligne : https://drive.google.com/file/d/1SJqmHAC8Nj95GNliW1XCmKH_fQtbEo33/view?usp=drive [...] Format de la ressource électronique : Permalink : https://e-campus.itech.fr/pmb/opac_css/index.php?lvl=notice_display&id=20547
in ADHESIVES AGE > Vol. 39, N° 12 (11/1996) . - p. 40-44[article]Exemplaires (1)
Code-barres Cote Support Localisation Section Disponibilité 001069 - Périodique Bibliothèque principale Documentaires Exclu du prêt Crosslinking of waterborne polyurethane dispersions / Valentino J. Tramontano in JOURNAL OF COATINGS TECHNOLOGY (JCT), Vol. 67, N° 848 (09/1995)
[article]
Titre : Crosslinking of waterborne polyurethane dispersions Type de document : texte imprimé Auteurs : Valentino J. Tramontano, Auteur ; Werner J. Blank, Auteur Année de publication : 1995 Article en page(s) : p. 89-99 Note générale : Bibliogr. Langues : Américain (ame) Catégories : Agents d'expansion (chimie)
Contraintes (mécanique)
Déformations (mécanique)
Dispersions et suspensions
Groupement carboxyle
HydroxyleEn chimie organique, un hydroxyle (ou oxhydryle) peut désigner deux entités.
Un groupement -OH, appelé aussi hydroxy, qui se rencontre en particulier dans les alcools et les phénols.
Un radical : HO^{\bullet}. Il est produit par exemple lors de réactions de dissociation de peroxydes, en présence d'ions de métaux de transition (Fe(II), Cu(I), réaction de Fenton), de chauffage ou de rayonnement.
MélamineLa mélamine, de nom chimique 1,3,5-triazine-2,4,6-triamine, est parfois dénommée cyanuramide ou cyanurotriamine. Sa formule brute est C3H6N6.
Les "résines mélamine-formaldéhyde" ou "mélamine-formol" (sigle MF) sont appelées "mélamine" dans le langage courant. Elles font partie de la famille des aminoplastes qui regroupe des résines thermodurcissables aminées, issues d'un comonomère tel l'urée ou la mélamine, parfois le thiocarbamide, le cyanamide hydrogène ou le dicyandiamide ; le second comonomère étant le formaldéhyde.
Polymères en émulsion
Polyuréthanes
Réticulation (polymérisation)
Revêtements en phase aqueuse:Peinture en phase aqueuse
Revêtements sans isocyanatesIndex. décimale : 667.9 Revêtements et enduits Résumé : A hydroxyl/carboxyl functional low molecular weight polyurethane dispersion was prepared by a nonisocyanate process. It was compared to a conventional high molecular weight polyurethane dispersion in films cured with melamine-formaldehyde resins. Stress-strain studies and solvent swelling experiments were used to characterize network formation and determine crosslink density. The morphology of the films prepared from the two types of polyurethanes were different, and coatings performance advantages were found with the low molecular weight polyurethane dispersion. Surface analysis by FTIR ATR indicates a more uniform distribution of melamine crosslinker in the cured low molecular weight polyurethane coating. Note de contenu : - EXPERIMENTAL: Materials - Coating formulations - Stress-strain measurements - Swelling experiments - FIT ATR surface analysis - Stain testing of coatings
- RESULTS AND DISCUSSION: Coating test results - Swelling experiments - Stress strain analysis of the free films - FTIR ATR analysis of free films - Stain test results of coatingsPermalink : https://e-campus.itech.fr/pmb/opac_css/index.php?lvl=notice_display&id=18553
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Code-barres Cote Support Localisation Section Disponibilité 003494 - Périodique Bibliothèque principale Documentaires Disponible 003506 - Périodique Bibliothèque principale Documentaires Exclu du prêt Effect of acid groups in hydroxyl functional resins on the properties of polyester-urethane powder coating / Bin Wu in JOURNAL OF COATINGS TECHNOLOGY (JCT), Vol. 72, N° 906 (07/2000)
[article]
Titre : Effect of acid groups in hydroxyl functional resins on the properties of polyester-urethane powder coating Type de document : texte imprimé Auteurs : Bin Wu, Auteur ; Sanjay Padaki, Auteur Année de publication : 2000 Article en page(s) : p. 55-62 Note générale : Bibliogr. Langues : Américain (ame) Catégories : Acidité
Couches minces
Essais de brouillard salin
Formulation (Génie chimique)
Groupement carboxyle
HydroxyleEn chimie organique, un hydroxyle (ou oxhydryle) peut désigner deux entités.
Un groupement -OH, appelé aussi hydroxy, qui se rencontre en particulier dans les alcools et les phénols.
Un radical : HO^{\bullet}. Il est produit par exemple lors de réactions de dissociation de peroxydes, en présence d'ions de métaux de transition (Fe(II), Cu(I), réaction de Fenton), de chauffage ou de rayonnement.
Liants
Polyesters
Polyuréthanes
Résistance aux conditions climatiques
Réticulation (polymérisation)
Revêtements -- Propriétés mécaniques:Peinture -- Propriétés mécaniques
Revêtements poudre:Peinture poudreIndex. décimale : 667.9 Revêtements et enduits Résumé : Hydroxyl-terminated polyester resins with different acid numbers were synthesized and used in powder coating formulations. Coatings were formulated with isophorone diisocyanate (IPDI)-based hardeners and tested for mechanical performance, appearance, and weathering. This study found that resins containing a high concentration of residual acid groups (also referred to as undercondensed resins) had to be formulated according to their total reactive number, the sum of acid and hydroxyl numbers, in order to achieve complete cure. High acid numbers also caused poor overbake and salt spray resistance. The addition of adipic or benzoic acids to the powder formulation accelerated cure. Note de contenu : - RESULTS AND DISCUSSION: Resins - Powder formulation - Curing chemistry - Effect of AN and crosslinker stoichiometry on curing - Acid catalysis - Effect of residual acid groups on coating properties - Overbake resistance - Salt fog testing (ASTM B 117) - Curing residual carboxyl groups Permalink : https://e-campus.itech.fr/pmb/opac_css/index.php?lvl=notice_display&id=17986
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