EP4267641A1 - Composition contenant un ester d'acide polyaspartique - Google Patents

Composition contenant un ester d'acide polyaspartique

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Publication number
EP4267641A1
EP4267641A1 EP21839529.1A EP21839529A EP4267641A1 EP 4267641 A1 EP4267641 A1 EP 4267641A1 EP 21839529 A EP21839529 A EP 21839529A EP 4267641 A1 EP4267641 A1 EP 4267641A1
Authority
EP
European Patent Office
Prior art keywords
component
acid ester
polyaspartic acid
composition
composition according
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Pending
Application number
EP21839529.1A
Other languages
German (de)
English (en)
Inventor
Fei Xu
Deyong ZHU
Jinqi Li
Yan Deng
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Covestro Deutschland AG
Original Assignee
Covestro Deutschland AG
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Priority claimed from CN202011541617.6A external-priority patent/CN114656866A/zh
Priority claimed from EP21161312.0A external-priority patent/EP4056617A1/fr
Application filed by Covestro Deutschland AG filed Critical Covestro Deutschland AG
Publication of EP4267641A1 publication Critical patent/EP4267641A1/fr
Pending legal-status Critical Current

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G18/00—Polymeric products of isocyanates or isothiocyanates
    • C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
    • C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
    • C08G18/30—Low-molecular-weight compounds
    • C08G18/38—Low-molecular-weight compounds having heteroatoms other than oxygen
    • C08G18/3819—Low-molecular-weight compounds having heteroatoms other than oxygen having nitrogen
    • C08G18/3821—Carboxylic acids; Esters thereof with monohydroxyl compounds
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G18/00—Polymeric products of isocyanates or isothiocyanates
    • C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
    • C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
    • C08G18/30—Low-molecular-weight compounds
    • C08G18/38—Low-molecular-weight compounds having heteroatoms other than oxygen
    • C08G18/3819—Low-molecular-weight compounds having heteroatoms other than oxygen having nitrogen
    • C08G18/3842—Low-molecular-weight compounds having heteroatoms other than oxygen having nitrogen containing heterocyclic rings having at least one nitrogen atom in the ring
    • C08G18/3851—Low-molecular-weight compounds having heteroatoms other than oxygen having nitrogen containing heterocyclic rings having at least one nitrogen atom in the ring containing three nitrogen atoms in the ring
    • C08G18/3853—Low-molecular-weight compounds having heteroatoms other than oxygen having nitrogen containing heterocyclic rings having at least one nitrogen atom in the ring containing three nitrogen atoms in the ring containing cyanurate and/or isocyanurate groups
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G18/00—Polymeric products of isocyanates or isothiocyanates
    • C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
    • C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
    • C08G18/30—Low-molecular-weight compounds
    • C08G18/38—Low-molecular-weight compounds having heteroatoms other than oxygen
    • C08G18/3855—Low-molecular-weight compounds having heteroatoms other than oxygen having sulfur
    • C08G18/3863—Low-molecular-weight compounds having heteroatoms other than oxygen having sulfur containing groups having sulfur atoms between two carbon atoms, the sulfur atoms being directly linked to carbon atoms or other sulfur atoms
    • C08G18/3865—Low-molecular-weight compounds having heteroatoms other than oxygen having sulfur containing groups having sulfur atoms between two carbon atoms, the sulfur atoms being directly linked to carbon atoms or other sulfur atoms containing groups having one sulfur atom between two carbon atoms
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G18/00—Polymeric products of isocyanates or isothiocyanates
    • C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
    • C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
    • C08G18/30—Low-molecular-weight compounds
    • C08G18/38—Low-molecular-weight compounds having heteroatoms other than oxygen
    • C08G18/3855—Low-molecular-weight compounds having heteroatoms other than oxygen having sulfur
    • C08G18/3876—Low-molecular-weight compounds having heteroatoms other than oxygen having sulfur containing mercapto groups
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G18/00—Polymeric products of isocyanates or isothiocyanates
    • C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
    • C08G18/70—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the isocyanates or isothiocyanates used
    • C08G18/72—Polyisocyanates or polyisothiocyanates
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G18/00—Polymeric products of isocyanates or isothiocyanates
    • C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
    • C08G18/70—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the isocyanates or isothiocyanates used
    • C08G18/72—Polyisocyanates or polyisothiocyanates
    • C08G18/77—Polyisocyanates or polyisothiocyanates having heteroatoms in addition to the isocyanate or isothiocyanate nitrogen and oxygen or sulfur
    • C08G18/78—Nitrogen
    • C08G18/79—Nitrogen characterised by the polyisocyanates used, these having groups formed by oligomerisation of isocyanates or isothiocyanates
    • C08G18/797—Nitrogen characterised by the polyisocyanates used, these having groups formed by oligomerisation of isocyanates or isothiocyanates containing carbodiimide and/or uretone-imine groups
    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
    • C09D175/00—Coating compositions based on polyureas or polyurethanes; Coating compositions based on derivatives of such polymers
    • C09D175/04—Polyurethanes
    • C09D175/12—Polyurethanes from compounds containing nitrogen and active hydrogen, the nitrogen atom not being part of an isocyanate group

Definitions

  • the invention relates to a polyaspartic acid ester-containing composition, a two-component coating composition containing the composition, a coating method and application of the coating composition, and a product obtained by applying the coating composition.
  • Polyaspartic acid ester-containing coating compositions and elastomers can be widely used in a variety of substrates to protect them and to improve their performance.
  • polyaspartic acid ester-containing coating compositions are widely used in industrial coating compositions due to their excellent corrosion resistance, wear resistance, chemical resistance and weather resistance.
  • the general disadvantage of polyaspartic acid ester-based coating compositions and elastomers is that polyaspartic acid ester has an obvious yellowing tendency during storage, which is undesirable during formulation design, storage and use.
  • sterically hindered phenol antioxidants such as 3, 5 -di -tert-butyl -4- hydroxytoluene
  • organic phosphite antioxidants such as trinonylphenyl phosphite, triphenyl phosphite, diphenyl isodecyl phosphite, diphenyl isooctyl phosphite, tridodecyl phophite and tris(2,4-di-tert-butyl-phenyl) phosphite are added to increase the color stability of polyaspartic acid ester-containing coating compositions or elastomers.
  • CN104449303B discloses that at least two antioxidants (TPP, BHT, TNPP, TEPA, Irganoxl 135 and triisodecyl phosphite) are used together to significantly improve the color stability of polyaspartic acid ester-containing coating compositions and the transparent coatings formed therefrom.
  • US2002132965A discloses that a thiol can be used as a co-reactant in the reaction of a primary amine and diethyl maleate for the synthesis of polyaspartic acid esters to increase the conversion in the synthesis of polyaspartic acid esters.
  • US2010311890A discloses that the thiol contained in low modulus polyaspartic acid ester- containing coating compositions can be used as a component that provides active hydrogen for other reaction resins (including polyethers, polyols, thiol ethers, polycarbonates and polyesters) in the reaction to generate polyurea coating compositions. It is desired to develop a polyaspartic acid ester-containing coating composition with high color stability and low yellowing tendency.
  • the objects of the present invention are to provide a polyaspartic acid ester-containing composition, a two-component coating composition containing the composition, a coating method and use of the coating composition, and a product obtained by applying the coating composition.
  • the polyaspartic acid ester-containing composition according to the present invention comprises: a. a polyaspartic acid ester; b. a thiol with an active hydrogen group; and c. optionally an antioxidant in an amount of not more than 3% by weight, relative to the total weight of the composition; wherein the molar ratio of mercapto groups of the thiol of component b) to amino groups of the polyaspartic acid ester of component a) is of 0.060-0.720.
  • a coating composition, an adhesive or a sealant comprising the polyaspartic acid ester-containing composition according to the present invention is provided .
  • a two-component coating composition comprising component A and component B is provided, wherein said component A is the polyaspartic acid ester-containing composition according to the present invention, and said component B is a crosslinking agent.
  • a coating method comprising applying the two-component coating composition according to the present invention to a surface of a substrate and then curing and drying is provided.
  • a product comprising a substrate and a coating formed by applying the two-component coating composition of the present invention to the substrate and then curing and drying is provided.
  • a method for preparing the polyaspartic acid ester-containing composition according to the present invention comprises mixing the polyaspartic acid ester of component a), the thiol with an active hydrogen group of component b) and optionally an antioxidant of component c) in any desired manner.
  • the thiol and optionally the antioxidant in the polyaspartic acid ester-containing composition of the present invention can effectively inhibit the yellowing of the composition, and thus the composition has high color stability.
  • a coating composition comprising the composition of the present invention, especially a transparent coating composition, can still have color stability and show unobvious yellowing after being stored for 20 weeks at the temperature of 50°C.
  • the present invention provides a polyaspartic acid ester-containing composition
  • a polyaspartic acid ester-containing composition comprising a. a polyaspartic acid ester; b. a thiol with an active hydrogen group; and c. optionally an antioxidant in an amount of not more than 3% by weight, relative to the total weight of the composition; wherein the molar ratio of mercapto groups of the thiol of component b) to amino groups of the polyaspartic acid ester of component a) is of 0.060-0.720.
  • the present invention also provides a method for preparing the composition, a two-component coating composition comprising the composition, a coating method and use of the coating composition, and a product obtained by applying the coating composition.
  • primary thiol refers to a thiol with a mercapto group attached to the primary position of the end group.
  • thiol used herein refers to an organic sulfur compound corresponding to the general formula R-SH, where R represents an alkyl group or other organic substituent, the sulfur atom being connected to a carbon atom.
  • two-component coating composition used herein refers to a coating composition comprising at least two components, which have to be stored in separate containers due to their reactivity with each other. When these two separate components are mixed and applied to a substrate, the reactive compounds in the two components react with each other to crosslink and form a cured coating.
  • coating composition refers to a chemical composition that can be applied to a surface of an object by a variety of application processes to form a continuous solid coating with firm adhesion and certain strength.
  • curing and drying refers to a process from a liquid state to a cured state of a coating composition.
  • each independently used herein means that the groups may be identical or different.
  • organic group non-reactive toward isocyanate refers to an organic group that is inert to isocyanate groups at a temperature of 100°C or lower.
  • Amino herein refers to -NR2, -NHR, R-NH2, where R is an alkyl group.
  • the polyaspartic acid ester-containing composition is preferably transparent.
  • the molar ratio of mercapto groups of the thiol of component b) to amino groups of the polyaspartic acid ester of component a) refers to the ratio of the mercapto group moles of the thiol of component b) to the amino group moles of the polyaspartic acid ester of component a).
  • the molar ratio of mercapto groups of the thiol of component b) to amino groups of the polyaspartic acid ester of component a) is preferably of 0.070-0.72, more preferably of 0.070-0.240, and most preferably of 0.070-0.200.
  • the calculation method is as follows:
  • the amount of the polyaspartic acid ester is preferably of 40% to 95% by weight, relative to the total weight of the composition.
  • the polyaspartic acid ester has preferably the structure of formula I:
  • R 1 and R 2 are each independently an organic group, which is non-reactive toward isocyanate groups under normal pressure and at a temperature of less than or equal to 100°C, n is an integer of not less than 2.
  • the aliphatic residue is preferably one or more of linear alkyl residues, branched alkyl residues and cycloalkyl residues, and most preferably cycloalkyl residues.
  • the aliphatic residue herein is preferably derived from an alcohol compound which is preferably one or more of ethylene glycol, 1,2-dihydroxypropane, 1,4-dihydroxybutane, 1,6- dihydroxyhexane, 2,2,4-and/or 2,4,4-trimethyl-l,6-dihydroxyhexane, 1 -hydroxy-3, 3,5- trimethyl-5-hydroxymethylcyclohexane, 4, 4'-dihydroxy di cyclohexylmethane, 3,3'- dimethyl-4',4'-dihydroxydicyclohexylmethane, 1,5 -dihydroxy -2 -methylpentane, 1,1,1- trimethylolpropane and 2,2-bis(hydroxymethyl)-l,3-propanediol (pentaerythritol).
  • an alcohol compound which is preferably one or more of ethylene glycol, 1,2-dihydroxypropane, 1,4-dihydroxybutane, 1,6- dihydroxyhexan
  • R 1 and R 2 are each independently preferably an alkyl residue having 1 to 10 carbon atoms, and most preferably one or more of methyl, ethyl and butyl.
  • n is preferably an integer of 2 to 4, and most preferably 2.
  • the polyaspartic acid ester is most preferably one or more of Desm ophen NH 1420, Desmophen 1520, Desmophen 1220, Desmophen 2872, Desmophen 2850, Desmophen 1422 and Desmophen 1521, all available from Covestro Polymers (China) Co., Ltd.
  • the amino equivalent of the polyaspartic acid ester is preferably of 200-500.
  • the viscosity of the polyaspartic acid ester is preferably of 500 to 4000 mPa s.
  • n of the polyaspartic acid ester is 2, it is obtained by the reaction of a polyamine of the following formula and a maleate and/or fumarate of the following formula:
  • the polyamine is preferably one or more of ethylenediamine, 1,2-diaminopropane, 1,4- diaminobutane, 1,3 -diaminopentane, 1,6-diaminohexane, 2,5-diamino-2,5-dimethylhexane,
  • the maleate and/or fumarate is preferably one or more of dimethyl maleate, diethyl maleate, dibutyl maleate, dimethyl fumarate, diethyl fumarate and dibutyl fumarate.
  • the reaction temperature is preferably of 0°C to 100°C.
  • the weight ratio of the maleate and/or fumarate to the polyamine is preferably 2:1.
  • the weight ratio of the olefinic double bonds of the maleate and/or fumarate to the primary amino groups of the polyamine is preferably 1 : 1.
  • the product obtained from the reaction is preferably purified by rectification.
  • the components of the reaction may or may not comprise a solvent, and preferably comprises a solvent.
  • the solvent is preferably one or more of methanol, ethanol, propanol and dioxane.
  • the amount of the thiol with an active hydrogen group of component b) is preferably of 3% by weight to 8% by weight, relative to the total weight of the composition.
  • the thiol of component b) is one or more of tris[2-(3-mercaptopropionyloxy)ethyl] isocyanurate, pentaerythritol tetra(3 -mercaptopropionate), bi s(2 -mercaptoethyl) sulfide, 2,3- bis[(2-mercaptoethyl)thio]-l-propanethiol, trimethylolpropane tri(2-mercaptoacetate), and pentaerythritol tetra(mercaptoacetate) .
  • the amount of the antioxidant is preferably of not more than 2% by weight, relative to the total weight of the composition.
  • composition does not comprise an antioxidant.
  • the antioxidant is preferably one or more of sterically hindered phenolic antioxidants and organic phosphite antioxidants; and most preferably one or more of triphenyl phosphite, trinonylphenyl phosphite, 3,5-di-tert-butyl-4-hydroxytoluene and isooctyl 3, 5 -di -tert-butyl - 4-hydroxyphenylpropionate.
  • the two-component coating composition is preferably transparent.
  • component A and component B of the two-component coating composition are preferably stored separately, and mixed prior to use to give the two-component coating composition.
  • Crosslinking agent of component B is preferably stored separately, and mixed prior to use to give the two-component coating composition.
  • the crosslinking agent is preferably one or more of isocyanate group-containing compounds and carbodiimides.
  • Isocyanate groups of the isocyanate group-containing compounds of the present invention include free and/or potentially free isocyanate groups.
  • the potentially free isocyanate groups can be released by a method well known to those skilled in the art, such as heating.
  • the isocyanate group-containing compound is preferably liquid at room temperature or becomes liquid by adding an organic solvent.
  • the isocyanate group-containing compound may comprise a blocked isocyanate group.
  • the blocked isocyanate group is blocked by reacting with a low molecular weight compound containing active hydrogen.
  • the low molecular weight compound containing active hydrogen may be a aliphatic alcohol, an alicyclic alcohol, a dialkylamino alcohol, oxime, lactam, imide, hydroxyalkyl ester, malonate or acetoacetate.
  • the isocyanate group-containing compound may have hydrophilic groups.
  • the isocyanate group-containing compound is preferably one or more of aliphatic polyisocyanates, alicyclic polyisocyanates, araliphatic polyisocyanates and aromatic polyisocyanates, most preferably one or more of aliphatic polyisocyanates and alicyclic polyisocyanates.
  • the isocyanate group-containing compound may be a prepolymer or an adduct of diisocyanate, for example, a trimer of diisocyanate.
  • the isocyanate group-containing compound may also be an isocyanurate, a biuret group-containing polyisocyanate, a urethane group-containing polyisocyanate, an allophanate group-containing polyisocyanate, an isocyanurate group- and allophanate group-containing polyisocyanate, a carbodiimide group-containing polyisocyanate, and a ureide group-containing polyisocyanate.
  • the equivalent ratio of the isocyanate groups of the isocyanate group-containing compound to the isocyanate-reactive groups of component A is preferably of 0.5: 1-10: 1.
  • the two-component coating composition may further comprise an additive.
  • the additive is selected from one or more of pigments such as organic pigments, inorganic pigments, metallic pigments or pearlescent pigments, wetting agents, matting agents, defoamers, film formers, thickeners, elastic agents, catalysts, UV absorbers, and other additives that can be added to the two-component coating composition as well known to those skilled in the art.
  • the additive may be added in an amount which is well known to those skilled in the art.
  • the two-component coating composition may further comprise a solvent.
  • the solvent may be one that can be added to the two-component coating composition as well known to those skilled in the art, most preferably one or more of n-butyl acetate, xylene and propylene glycol methyl ether acetate.
  • the solvent may be added in an amount which is well known to those skilled in the art.
  • the substrate may be artificial stone, wood, artificial wood, marble, terrazzo, ceramic, felt, metal, plastic, rubber, concrete, composite board, paper, leather or glass, most preferably metal or glass.
  • the substrate may be pre-treated.
  • the pre-treatment may be polishing or coating.
  • the application may be a method well known to those skilled in the art, such as knife coating, brush coating, roller coating, spray coating or curtain coating.
  • the product can be windows, mirrors, furniture, bicycles, cars, road signs, bridges, books or boxes, most preferably cars.
  • the isocyanate group (NCO) content is determined by volume in accordance with DIN-EN ISO 11909.
  • the measured data include free and potentially free NCO contents.
  • Hazen value is measured by using Hazen tester of Hash LICO 690 equipment according to ASTMD1209 standard.
  • Hazen tester of Hash LICO 690 equipment according to ASTMD1209 standard.
  • Desmophen NH1520 polyaspartic acid ester having a solid content of 100% by weight with amino functionality of 2.0 and amino equivalent of 290, available from Covestro Co., Ltd., Germany.
  • TEMPIC tris[2-(3-mercaptopropionyloxy)ethyl] isocyanurate, thiol, from Bruno Bock-DE.
  • PETMP pentaerythritol tetra(3 -mercaptopropionate), thiol, from Bruno Bock-DE.
  • GST 2,3-bis[(2-mercaptoethyl)thio]-l-propanethiol, thiol, from Bruno Bock-DE.
  • DMDS bi s(2 -mercaptoethyl) sulfide, thiol, from Bruno Bock-DE.
  • TPP Triphenyl phosphite, antioxidant, from Shanghai Macklin Biochemical Co., Ltd.
  • BHT 3,5-di-tert-butyl-4-hydroxytoluene, antioxidant, from Sigma-Aldrich (Shanghai), n-butyl acetate: solvent, from Shanghai Ling Feng Chemical reagent Co. Ltd.
  • BYK-333 Surface active agent, from BYK.
  • BYK-141 Defoamer, from BYK.
  • BYK-358N Wetting agent, from BYK.
  • Table 1 shows the TEMPIC content, the initial color value and the color value after several weeks of storage at 50°C of the polyaspartic acid ester-containing compositions from Examples 1-2 and Comparative Examples 1-4.
  • Table 2 shows the PETMP content, the initial color value and the color value after several weeks of storage at 50°C of the polyaspartic acid ester-containing compositions from Examples 3-5 and Comparative Examples 1, 5 and 6.
  • Table 3 shows the GST content, the initial color value and the color value after several weeks of storage at 50°C of the polyaspartic acid ester-containing compositions from Examples 6- 9 and Comparative Examples 1 and 7.
  • Table 4 shows the DMDS content, the initial color value and the color value after several weeks of storage at 50°C of the polyaspartic acid ester-containing compositions from Examples 10-14 and Comparative Example 1.
  • Table 5 shows the composition, the initial color value and the color value after several weeks of storage at 50°C of the polyaspartic acid ester-containing compositions from Examples 14- 15 and Comparative Examples 1, and 8-9.
  • Table 6 shows the composition, the initial color value and the color value after several weeks of storage at 50°C of the polyaspartic acid ester-containing compositions from Examples 14 and 16 and Comparative Examples 1 and 10.
  • the initial Hazen values in the table below refer to the Hazen values obtained by the color value test within 60 minutes after the compositions have been prepared.
  • 6 weeks, 8 weeks, 15 weeks and 20 weeks indicate respectively that the Hazen values were obtained by the color value test after the compositions have been prepared and stored at 50°C for 6 weeks, 8 weeks, 15 weeks and 20 weeks.
  • Table 1 polyaspartic acid ester-containing compositions of Examples 1 to 2 and Comparative Examples 1 to 4 and color values thereof It can be seen from the comparation between Comparative Examples 1-4 with Examples 1- 2 that the color value of the composition after being stored at 50°C for 15 weeks was less than 150, that is, the composition was color stable and not prone to yellowing, when the molar ratio of mercapto groups of the thiol TEMPIC to amino groups of the polyaspartic acid ester in the transparent composition containing polyaspartic acid ester was greater than 0.060.
  • Comparative Examples 1 and 8 It can be seen from Comparative Examples 1 and 8 that the color value of the composition after being stored at 50°C for 15 weeks was much higher than 150, that is, the composition had poor color stability and was prone to yellowing, when the composition comprised no thiol.
  • the 5% by weight of antioxidant in the composition of Comparative Example 8 could not improve the color stability of the composition.
  • Comparative Examples 1 and 10 that the color value of the composition after being stored at 50°C for 15 weeks was much higher than 150, that is, the composition had poor color stability and was prone to yellowing, when the composition comprised no thiol.
  • the 5% by weight of antioxidant in the composition of Comparative Example 10 could not improve the color stability of the composition.
  • the color value of the transparent composition containing polyaspartic acid ester after being stored at 50°C for 15 weeks was much less than 150, that is, the composition was color stable and not prone to yellowing, when the molar ratio of mercapto groups of DMDS to amino groups of the polyaspartic acid ester in the composition was greater than 0.060 and the antioxidant content of the composition was 1.67 % by weight and 0 % by weight.

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  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
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  • Paints Or Removers (AREA)

Abstract

L'invention concerne une composition contenant un ester d'acide polyaspartique, une composition de revêtement à deux constituants contenant ladite composition, un procédé d'application de revêtement et l'utilisation de la composition de revêtement, et un produit obtenu par l'application de la composition de revêtement. La composition contenant un ester d'acide polyaspartique comprend a. un ester d'acide polyaspartique ; b. un thiol comportant un groupe à hydrogène actif ; et c. éventuellement un antioxydant en une proportion inférieure ou égale à 3 % en poids, par rapport au poids total de la composition ; le rapport molaire des groupes mercapto du thiol du constituant b) aux groupes amino de l'ester d'acide polyaspartique du constituant a) est de 0,060 à 0,720. La composition selon la présente invention présente une stabilité de couleur élevée et n'est pas sujette au jaunissement.
EP21839529.1A 2020-12-23 2021-12-17 Composition contenant un ester d'acide polyaspartique Pending EP4267641A1 (fr)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
CN202011541617.6A CN114656866A (zh) 2020-12-23 2020-12-23 一种含聚天门冬氨酸酯的组合物
EP21161312.0A EP4056617A1 (fr) 2021-03-08 2021-03-08 Composition contenant des esters d'acide polyaspartique
PCT/EP2021/086427 WO2022136155A1 (fr) 2020-12-23 2021-12-17 Composition contenant un ester d'acide polyaspartique

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DE10050137A1 (de) 2000-10-11 2002-04-18 Bayer Ag Stabilisierte Mono- und Polyasparaginsäureester
US20100311890A1 (en) 2009-06-05 2010-12-09 Ppg Industries Ohio, Inc. Curable compositions that form a low modulus polyurea
US9790399B2 (en) 2013-07-23 2017-10-17 Axalta Coatings Systems Ip Co. Llc Clear coat component
EP3029129A1 (fr) * 2014-12-04 2016-06-08 HILTI Aktiengesellschaft Composition formant une couche isolante et son utilisation
EP3677609A1 (fr) * 2019-01-03 2020-07-08 Sika Technology Ag Composition de polyurée pulvérisable pour la protection contre la corrosion

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