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EP4388025A1 - Nouveaux systèmes de revêtement à deux composants contenant des esters d'acide polyaspartique - Google Patents

Nouveaux systèmes de revêtement à deux composants contenant des esters d'acide polyaspartique

Info

Publication number
EP4388025A1
EP4388025A1 EP22765763.2A EP22765763A EP4388025A1 EP 4388025 A1 EP4388025 A1 EP 4388025A1 EP 22765763 A EP22765763 A EP 22765763A EP 4388025 A1 EP4388025 A1 EP 4388025A1
Authority
EP
European Patent Office
Prior art keywords
component
coating
weight
polyaspartic acid
general formula
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
EP22765763.2A
Other languages
German (de)
English (en)
Inventor
Erkan DURGUT
Dorota Greszta-Franz
Matthias Wintermantel
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
Application filed by Covestro Deutschland AG filed Critical Covestro Deutschland AG
Publication of EP4388025A1 publication Critical patent/EP4388025A1/fr
Pending legal-status Critical Current

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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
    • C08G18/70—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the isocyanates or isothiocyanates used
    • C08G18/72—Polyisocyanates or polyisothiocyanates
    • C08G18/73—Polyisocyanates or polyisothiocyanates acyclic
    • 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
    • C09D175/02—Polyureas
    • 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
    • C08G18/08—Processes
    • C08G18/10—Prepolymer processes involving reaction of isocyanates or isothiocyanates with compounds having active hydrogen in a first reaction step
    • 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
    • C08G18/70—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the isocyanates or isothiocyanates used
    • C08G18/72—Polyisocyanates or polyisothiocyanates
    • C08G18/721—Two or more polyisocyanates not provided for in one single group C08G18/73 - C08G18/80
    • 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
    • C08G18/791—Nitrogen characterised by the polyisocyanates used, these having groups formed by oligomerisation of isocyanates or isothiocyanates containing isocyanurate groups
    • C08G18/792—Nitrogen characterised by the polyisocyanates used, these having groups formed by oligomerisation of isocyanates or isothiocyanates containing isocyanurate groups formed by oligomerisation of aliphatic and/or cycloaliphatic isocyanates or isothiocyanates
    • 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
    • C08G18/798—Nitrogen characterised by the polyisocyanates used, these having groups formed by oligomerisation of isocyanates or isothiocyanates containing urethdione 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

Definitions

  • the present invention relates to two-component coating systems containing polyaspartic esters with only small amounts of dialkyl fumarate, a process for their production and their use for the production of coatings, in particular for the construction and wind energy sectors.
  • the use for roof coating, for floor coating and for coating rotor blades in wind turbines, or their leading edges, may be mentioned as an example.
  • Two-component (2K) coating compositions which contain as binder a polyisocyanate component in combination with a reactive component which is capable of reacting with isocyanate groups, in particular a polyhydroxyl component, have been known for a long time. They are suitable for the production of high-quality coatings that can be made hard, elastic, resistant to abrasion and solvents and, above all, weatherproof.
  • Certain secondary polyamines containing ester groups have recently become established within this 2-component polyurethane coating technology.
  • they are particularly suitable as binders in low-solvent or solvent-free (high solids) coating materials and ensure rapid curing of the coatings at low temperatures.
  • amino-functional aspartic acid esters is known per se.
  • the synthesis takes place via an addition of primary polyamines and/or polyetheramines to an activated carbon double bond of vinylogous carbonyl compounds, such as those contained in maleic or fumaric acid e systems, which is adequately described in the literature (Hauben Weyl, Meth. d. Org. Chemie Vol. 11/1, 272 (1957), Usp. Khim. 1969, 38, 1933).
  • a polyaspartic acid ester with primary amino groups can be formed as a by-product if only one amino group of the polyamine/polyetheramine has reacted with the double bond of the vinylogous carbonyl compounds.
  • maleic ester is used as the vinylogous carbonyl compound.
  • retro-Michael addition can occur as another undesirable side reaction, in which elimination of the polyamine as Secondary component fumaric acid dialkyl ester is formed.
  • a typical manufacturing process for a polyaspartic acid ester therefore requires a storage time of 4-6 weeks after the majority of the starting materials have reacted with one another. During this time, the so-called maturation of the product takes place, which manifests itself in the stabilization of the viscosity. Because the conversion continues to increase during this time, the dialkyl fumarate content also decreases.
  • WO2019/057626A1 and WO2019/057627A1 disclose the production of polyaspartic acid esters with a significantly reduced dialkyl fumarate content by means of a special distillation process.
  • polyaspartic acid esters can be used to produce low-solvent or solvent-free (high solids) coating compositions. This is an essential aspect in relation to industrial hygiene, especially when working in closed rooms, for example when coating floors.
  • Polyaspartic acid esters can be divided into those based on (ether group-free) polyamines and those based on polyetheramines. Polyaspartic esters based on polyetheramines have a significantly lower viscosity than polyaspartic esters based on polyamines. Polyetheramine-based polyaspartic esters can therefore be used as diluents for polyamine-based polyaspartic esters. In this way, solvents can be saved or can be dispensed with entirely.
  • the object of the present invention was to provide a coating composition based on polyaspartic acid ester mixtures for producing coatings with improved mechanical properties, such as improved tensile strength and tear propagation strength. Surprisingly, it was found that this object can be achieved by coating compositions based on polyaspartic ester mixtures with a greatly reduced dialkyl fumarate content.
  • the dialkyl fumarate content in the component containing polyaspartic ester is 0.02 to 0.75% by weight, based on the total weight of the component containing polyaspartic ester, and can be reduced to these values by a special distillation process.
  • WO2019/057626A1 describes not only the production of polyaspartic acid esters with a significantly reduced dialkyl fumarate content but also their use in coating compositions.
  • the synthesis of polyamine-based and polyetheramine-based polyaspartic acid esters is shown.
  • the specific use of a mixture of both classes of compounds for the production of coating compositions is not disclosed; even less that a greatly reduced content of fumaric acid dialkyl esters in these mixtures leads to coatings with very high tensile strength and tear propagation strength.
  • WO2020/169700A1 and WO2020/169701A1 also describe coating compositions based on polyaspartic esters with a reduced dialkyl fumarate content.
  • polyaspartic esters with a reduced dialkyl fumarate content.
  • the use of polyamine-based or polyetheramine-based polyaspartic acid esters is described, but not the specific use of mixtures thereof.
  • the present invention relates to two-component coating compositions (2K coating compositions) containing a) at least one polyaspartic acid ester-containing component A, b) at least one polyisocyanate component B c) optionally one or more isocyanate-reactive components C that are different from A, and d) optionally auxiliaries and additives D, where component A corresponds to compositions containing
  • Heteroatom-containing organic radical as can be obtained by removing the primary amino groups from a corresponding polyamine having (cyclo)aliphatic or araliphatic bonded primary amino groups and having a molecular weight in the range from 60 to 6000 g/mol, and the further isocyanate-reactive and/or or can contain inert functional groups at temperatures up to 100°C,
  • R 1 and R 2 are identical or different organic radicals, each having 1 to 18 carbon atoms, m is an integer >1, preferably 2, and optionally one or more polyaspartic esters with a primary amino group of the general formula (II) in which n stands for m-1, and m, X and the radicals R 1 and R 2 have the meanings given above, and
  • Z is a p-valent, optionally one or more
  • Heteroatoms-containing organic radical is, as it is by removing the primary amino groups from a corresponding, aliphatically bonded primary amino groups having polyetherpolyamine of
  • R 3 and R 4 are identical or different organic radicals, each having 1 to 18 carbon atoms, p is an integer >1, preferably 2 or 3, component A2 in a proportion of >1 to ⁇ 80% by weight , based on the total weight of components A1 and A2, is present, and wherein component A contains dialkyl fumarate in an amount of >0.02 to ⁇ 0.75% by weight, based on the total weight of component A.
  • the dialkyl fumarate content is determined as detailed below in the experimental section.
  • polyetherpolyamines do not belong to the class of compounds of polyamines.
  • compositions containing polyaspartic acid esters are preferred, containing as component Al one or more polyaspartic acid esters of the general formulas (I) and optionally (II) in which R 1 and R 2 are identical or different alkyl radicals each having 1 to 18 carbon atoms, preferably identical or various alkyl radicals each having 1 to 8 carbon atoms and very particularly preferably each alkyl radicals such as methyl, ethyl, propyl, isopropyl, butyl or isobutyl radicals. Most preferred is ethyl.
  • Components A containing polyaspartic acid esters are compositions containing one or more polyaspartic acid esters of the general formulas (I) and optionally (II) as component A1, in which X represents organic radicals obtained by removing the primary amino groups from a corresponding polyamine containing primary amino groups are obtained, selected from the following group: all known polyamines with primary amino groups, which have the general formula (IV) match where
  • X is an m-valent organic radical optionally containing one or more heteroatoms, as obtained by removing the primary amino groups from a polyamine having (cyclo)aliphatic or araliphatic bonded primary amino groups and having a molecular weight in the range from 60 to 6000 g/mol and which can contain further functional groups which are reactive towards isocyanate groups and/or are inert at temperatures up to 100° C., and m is an integer >1, preferably 2.
  • ethylenediamine 1,2-diaminopropane, 1,4-diaminobutane, 1,5-diaminopentane, 2,5-diamino-2,5-dimethylhexane, 1,5-diamino-2-methylpentane (Dytek ®A, Invista), 1,6-diaminohexane, 2,2,4- and/or 2,4,4-trimethyl-1,6-diaminohexane, 1,11-diaminoundecane, 1,12-diaminododecane or triaminononane.
  • aliphatic polycyclic polyamines such as tricyclodecanebismethylamine (TCD-diamine) or bis(aminomethyl)norbomane, amino-functional siloxanes, e.g. diaminopropylsiloxane G10 DAS (Momentive), fatty alkyl-based amines, such as e.g. Fentamine from Solvay, dimer fatty acid diamines such as Priamine from Croda.
  • TCD-diamine tricyclodecanebismethylamine
  • amino-functional siloxanes e.g. diaminopropylsiloxane G10 DAS (Momentive)
  • fatty alkyl-based amines such as e.g. Fentamine from Solvay
  • dimer fatty acid diamines such as Priamine from Croda.
  • polyaspartic acid ester-containing components A compositions containing as component Al one or more polyaspartic acid esters of the general formulas (I) and optionally (II) in which X is organic radicals which are obtained by removing the primary amino groups from one of the polyamines of the general formula (IV), selected from the group: 1,2-diaminopropane, 1,4-diaminobutane, 1,5-diaminopentane, 1,6-diaminohexane, 1,5-diamino-2-methylpentane, 2,5-diamino- 2,5-dimethylhexane, 2,2,4- and/or 2,4,4-trimethyl-1,6-diaminohexane, 1,11-diaminounodecane, 1,12-diaminododecane, 1-amino-3,3,5 - trimethyl-5-aminomethylcyclohexane, 2,4- and/or
  • compositions containing polyaspartic acid esters are very particularly preferred, containing one or more polyaspartic acid esters of the general formulas (I) and optionally (II) as component Al, in which X represents organic radicals which are obtained by removing the primary amino groups from one of the polyamines general formula (IV), selected from the group: 3,3'-dimethyl-4,4'diaminodicyclohexylmethane, 2,4'- and/or 4,4'-diaminodicyclohexylmethane, 1,5-diamino-2-methylpentane .
  • X represents organic radicals which are obtained by removing the primary amino groups from one of the polyamines general formula (IV), selected from the group: 3,3'-dimethyl-4,4'diaminodicyclohexylmethane, 2,4'- and/or 4,4'-diaminodicyclohexylmethane, 1,5-diamino-2-methylp
  • Index m stands for an integer >1 and preferably for 2.
  • Component A compositions containing polyaspartic acid esters are preferred, containing as component A2 one or more polyaspartic acid esters of the general formula (III) in which R 3 and R 4 are identical or different alkyl radicals each having 1 to 18 carbon atoms, preferably identical or different alkyl radicals each having 1 up to 8 carbon atoms and very particularly preferably each alkyl radicals such as methyl, ethyl, propyl, isopropyl, butyl or isobutyl radicals. Most preferred is ethyl.
  • Components A containing polyaspartic acid esters are compositions containing, as component A2, one or more polyaspartic acid esters of the general formula (III) in which Z represents organic radicals obtained by removing the primary amino groups from a corresponding polyetherpolyamine containing primary amino groups the following group: all known polyetherpolyamines with primary amino groups, which have the general formula (V)
  • Z is a p-valent organic radical optionally containing one or more heteroatoms, as can be obtained by removing the primary amino groups from a corresponding polyetherpolyamine having aliphatically bonded primary amino groups and having a molecular weight in the range from 200 to 2000 g/mol, and the further, functional groups which are reactive toward isocyanate groups and/or functional groups which are inert at temperatures of up to 100° C., and p is an integer >1, preferably 2 or 3.
  • low molecular weight polyetherpolyamines such as 4,9-dioxadodecane-1,12-diamines and 4,7,10-trioxatridecane-1,13-diamines
  • higher molecular weight polyetherpolyamines with aliphatically bonded primary amino groups include, for example, compounds which have at least one repeating unit of the following general formula (VI): wherein r is a number from 2 to 35 and R 5 and R 6 are independently hydrogen or one
  • Ci - are to C4-alkyl radical.
  • Preferred polyethers containing amino groups of this type correspond to the following general formulas (VII) to (X)
  • polyetherpolyamines which i) have the formula (VIII) in which x is a number from 2 to 8, in particular from 2.5 to 6.1.
  • These polyetherpolyamines correspond, for example, to polyetherpolyamines from the JEFFAMINE® D series from Huntsman Corporation, in particular JEFFAMINE® D-230 and JEFFAMINE® D-400.
  • ii) of the formula (IX) correspond to where y is a number from 5 to 40 and the sum of x + z is a number from 3 to 8.
  • These polyetherpolyamines correspond, for example, to the JEFF AMINE® ED series polyetherpolyamines from Huntsman Corporation.
  • y is about 9.0 and x + z is about 3.6 or y is about 12.5 and x + z is about 6.0 (corresponding to, for example, JEFF AMINE® ED-600 and JEFF AMINE® ED-900, respectively ).
  • Components A containing polyaspartic acid esters are compositions containing a component A1 and a component A2, where component A2 is >1 to ⁇ 80% by weight, preferably >10 to ⁇ 80% by weight, particularly preferably >25 to ⁇ 55% by weight, very particularly preferably >30 to ⁇ 50% by weight, based on the total weight of components A1 and A2.
  • Components A containing polyaspartic acid esters are compositions containing one or more polyaspartic acid esters of the general formula (I) and optionally formula (II) and of the general formula (III) in a proportion >0.02 to ⁇ 0.75% by weight, preferably >0.02 to ⁇ 0.27% by weight, more preferably >0.02 to ⁇ 0.25% by weight, even more preferably >0.02 to ⁇ 0.1% by weight, most preferably >0.01 to ⁇ 0.05% by weight, based on the total weight of component A, of dialkyl fumarates.
  • component A compositions containing polyaspartic acid ester where component A2 is >1 to ⁇ 80% by weight, preferably >10 to ⁇ 80% by weight, particularly preferably >25 to ⁇ 55% by weight, very particularly preferably >30 to ⁇ 50% by weight, based on the total weight of components A1 and A2, and dialkyl fumarate in a proportion >0.02 to ⁇ 0.75% by weight, based on the total weight of component A , are included.
  • Component A compositions containing polyaspartic acid ester are even more preferred, where component A2 is present in a proportion >1 to ⁇ 80% by weight, preferably >10 to ⁇ 80% by weight, particularly preferably >25 to ⁇ 55% by weight, very particularly preferably >30 to ⁇ 50% by weight, based on the total weight of components Al and A2, and dialkyl fumarate with a proportion of >0.02 to ⁇ 0 25% by weight, based on the total weight of component A, are included.
  • Component A compositions containing polyaspartic acid esters are most preferred, with component A2 in a proportion >1 to ⁇ 80% by weight, preferably >10 to ⁇ 80% by weight, particularly preferably >25 to ⁇ 55% by weight, very particularly preferably >30 to ⁇ 50% by weight, based on the total weight of components A1 and A2, is present, and dialkyl fumarate in a proportion >0.02 to ⁇ 0.05% by weight, based on the total weight of the component A, are included.
  • the polyaspartic acid ester-containing component A1 contains one or more polyaspartic acid esters of the general formula (II), this/these are in a proportion of >0%, preferably >0.1%, particularly preferably >1%, very particularly preferably > 4%, and preferably ⁇ 20%, particularly preferably ⁇ 15% of the GC surface (measured as area % in the gas chromatogram), the sum of the GC surfaces of the compounds of the two general formulas (I) and (II) being 100 % amounts to.
  • the specified upper and lower limits can be combined as desired. All possible combinations are considered disclosed.
  • Components A containing polyaspartic acid esters are preferred compositions containing one or more polyaspartic acid esters of the general formula (I) and optionally formula (II) and of the general formula (III), where the esters have a platinum-cobalt color number ⁇ 200, particularly preferably ⁇ 100 exhibit.
  • the platinum-cobalt color number is measured in accordance with DIN EN ISO 6271:2016-05.
  • Components Al containing polyaspartic acid esters, containing one or more polyaspartic acid esters of the general formula (I) and formula (II), can be prepared by the following process: Reaction of polyamines of the general formula (IV), where X is an m-valent organic radical optionally containing one or more heteroatoms, such as can be obtained by removing the primary amino groups from a polyamine having (cyclo)aliphatic or araliphatic bonded primary amino groups and having a molecular weight in the range from 60 to 6000 g/mol , and which may contain other functional groups that are reactive toward isocyanate groups and/or that are inert at temperatures of up to 100° C., m is an integer >1, preferably 2, with compounds of the general formula (XI)
  • R 1 OOC - CH CH - COOR 2 ZVT , where R 1 and R 2 are identical or different organic radicals, preferably identical or different alkyl radicals each having 1 to 18 carbon atoms, particularly preferably identical or different alkyl radicals each having 1 to 8 Carbon atoms, very particularly preferably each alkyl radicals such as methyl, ethyl, propyl, isopropyl, butyl or isobutyl radicals and most preferably ethyl, and a distillative removal of the unreacted portion of the compound of the general formula (XI).
  • R 1 and R 2 are identical or different organic radicals, preferably identical or different alkyl radicals each having 1 to 18 carbon atoms, particularly preferably identical or different alkyl radicals each having 1 to 8 Carbon atoms, very particularly preferably each alkyl radicals such as methyl, ethyl, propyl, isopropyl, butyl or isobutyl radicals and most preferably ethyl
  • the following compounds may be mentioned as examples of compounds of the general formula (XI): dimethyl maleate, diethyl maleate, di-n-maleate or iso-propyl maleate, di-n-butyl maleate, di-2-ethylhexyl maleate or the corresponding fumaric acid esters.
  • Maleic acid diethyl ester is very particularly preferred.
  • the above-described process for preparing the polyaspartic acid ester-containing components A1, containing one or more polyaspartic acid esters of the general type, is preferably carried out Formula (I) and formula (II), in two steps.
  • Components Al containing polyaspartic acid esters which only contain polyaspartic acid esters of the general formula (I), but not of the formula (II), can be prepared analogously, but with a large excess of compounds of the general formula (XI), i.e. in a Ratio of the equivalents of the primary amino groups of the compounds of the general formula (IV) to the C ⁇ C double bond equivalents of the compounds of the general formula (XI) of 1:10, preferably 1:5, particularly preferably 1:2.
  • Suitable conditions during the distillation are a pressure range between 0.01 and 2 mbar and a temperature of the bottom discharge at the exit from the distillation apparatus of ⁇ 170°C and > the temperature that results from the following formula (1):
  • T(bottom outflow) 27 ⁇ ln(p)+150 (1)
  • T(bottom outflow) stands for the temperature of the bottom outflow in °C and p for the pressure in the distillation apparatus in mbar.
  • Maintaining this pressure range ensures that, on the one hand, moderate temperatures in the bottom outflow are sufficient to deplete the desired amount of dialkyl fumarate and, on the other hand, that the process can still be used on an industrial scale. At lower pressures, the gas density is too low and the equipment required is therefore so large that the process becomes disadvantageous from an economic point of view.
  • the temperature of the bottom discharge is preferably ⁇ 170° C., but at least 20 K above the temperature that results from formula (1), it is particularly preferably between 20 K and 40 K above the temperature that results from formula ( 1) does not result above 170°C.
  • Components A2 containing polyaspartic acid ester can be produced analogously to components A1 containing polyaspartic acid ester
  • Z is a p-valent organic radical optionally containing one or more heteroatoms, such as can be obtained by removing the primary amino groups from a corresponding polyetherpolyamine having aliphatically bonded primary amino groups and having a molecular weight in the range from 200 to 2000 g/mol , and which may contain other functional groups that are reactive toward isocyanate groups and/or that are inert at temperatures up to 100° C.
  • p is an integer >1, preferably 2 or 3, with compounds of the general formula (XII)
  • R 3 and R 4 are identical or different alkyl radicals each having 1 to 18 carbon atoms, preferably identical or different alkyl radicals each having 1 to 8 carbon atoms and very particularly preferably each alkyl radicals such as methyl, ethyl, propyl, isopropyl, Butyl or iso-butyl radicals and most preferably ethyl, and a distillative removal of the unreacted portion of the compound of general formula (XII).
  • the following compounds may be mentioned as examples of compounds of the general formula (XII): dimethyl maleate, diethyl maleate, di-n-maleate or iso-propyl maleate, di-n-butyl maleate, di-2-ethylhexyl maleate or the corresponding fumaric acid esters.
  • Maleic acid diethyl ester is very particularly preferred.
  • the unreacted portion of the compound of general formula (XII) is removed by distillation.
  • distillation conditions the statements made above for the preparation of components A1 containing polyaspartic acid esters apply analogously.
  • Component A can be obtained by mixing the individually synthesized components A1 and A2.
  • the mixing ratio of the compounds of general formula (IV) and (V) in the first step is preferably >1 to ⁇ 80% by weight, preferably >10 to ⁇ 80% by weight, particularly preferably >25 to ⁇ 55% by weight. -%, very particularly preferably >30 to ⁇ 50% by weight of the compound of general formula (V), based on the total weight of the compounds of general formula (IV) and (V).
  • the two-component coating compositions according to the invention contain at least one polyisocyanate component B.
  • Suitable polyisocyanate components B are organic polyisocyanates with an average NCO functionality of at least 2 and a molecular weight of at least 140 g/mol. Particularly suitable are unmodified organic polyisocyanates with a molecular weight in the range from 140 to 300 g/mol, paint polyisocyanates with a molecular weight in the range from 300 to 1000 g/mol, and NCO prepolymers containing urethane, urea and/or allophanate groups and having a molecular weight of more than 400 g/mol. mol lying molecular weight or mixtures thereof.
  • backpolyisocyanates is understood to mean compounds or mixtures of compounds which can be obtained by known oligomerization reactions of simple polyisocyanates.
  • suitable oligomerization reactions are carbodiimidization, dimerization, trimerization, biuretization, urea formation, urethanization, allophanatization and/or cyclization with the formation of oxadiazine structures.
  • oligomerization several of the reactions mentioned can take place simultaneously or one after the other.
  • the "Eack polyisocyanates” are preferably biuret polyisocyanates, polyisocyanates containing isocyanurate groups, polyisocyanate mixtures containing isocyanurate and uretdione groups, polyisocyanates containing urethane and/or allophanate groups, or polyisocyanate mixtures containing isocyanurate and allophanate groups and based on simple organic polyisocyanates.
  • polyisocyanate component B are also suitable as polyisocyanate component B.
  • polyisocyanate component B are the known prepolymers containing isocyanate groups based on simple organic polyisocyanates and/or based on bulk polyisocyanates on the one hand and organic polyhydroxy compounds with a molecular weight above 300 g/mol on the other.
  • Eackpolyisocyanates containing urethane groups are derivatives of low molecular weight polyols in the molecular weight range from 62 to 300 g/mol
  • suitable polyols are, for example, ethylene glycol, propylene glycol, trimethylolpropane, glycerol or mixtures of these alcohols
  • Polyhydroxy compounds containing isocyanate groups and having a molecular weight of more than 300 g/mol, preferably more than 400 g/mol, particularly preferably between 400 and 8000 g/mol, are used.
  • Such polyhydroxyl compounds are in particular those which have 2 to 6, preferably 2 to 3, hydroxyl groups per molecule and are selected from the group consisting of ether, ester, thioether, carbonate and polyacrylate polyols and mixtures of such polyols.
  • the higher molecular weight polyols mentioned can also be used in mixtures with the lower molecular weight polyols mentioned, so that mixtures of low molecular weight paint polyisocyanates containing urethane groups and higher molecular weight NCO prepolymers result directly, which are also suitable as polyisocyanate component b) according to the invention .
  • Suitable simple organic polyisocyanates are 1,4-diisocyanatobutane, 1,5-diisocyanatopentane, 1,6-diisocyanatohexane (HDI), 1,5-diisocyanato-2,2-dimethylpentane, 2,2,4- or 2, 4,4-Trimethyl-l,6-diisocyanatohexane, tetramethylxylylene diisocyanate (TMXDI) 1- isocyanato-3,3,5-trimethyl-5-isocyanatomethylcyclohexane (isophorone diisocyanate, IPDI), 1- isocyanato- 1 -methyl -4-(3) -isocyanatomethylcyclohexane, dicyclohexylmethane-2,4'- and/or 4,4'-diisocyanate, 1,10-diisocyanatodecane, 1,12-diisocyanatododecane,
  • the two-component composition according to the invention can contain other components (components C) which are reactive toward isocyanate groups.
  • polystyrene resin can be, for example, low molecular weight polyols in the molecular weight range from 62 to 300 g/mol, for example ethylene glycol, propylene glycol, trimethylolpropane, glycerol or mixtures of these alcohols, or polyhydroxy compounds of more than 300 g/mol, preferably more than 400 g/mol, particularly preferably one between 400 and 8000 g/mol molecular weight.
  • polyhydroxyl compounds are in particular those which have 2 to 6, preferably 2 to 3, hydroxyl groups per molecule and are selected from the group consisting of ether, ester, thioether, carbonate and polyacrylate polyols and mixtures of such polyols.
  • the two-component composition according to the invention can contain auxiliaries and additives D.
  • pigments such as titanium dioxide, zinc oxide, iron oxides, chromium oxides or carbon black
  • fillers such as barite, chalk or talc.
  • the auxiliaries and additives D also include catalysts/activators such as, for example, catalysts containing titanium, zirconium, bismuth, tin and/or iron, as they are, for example, in WO 05058996 are described. It is also possible to add amines or amidines.
  • the proportion of crosslinking catalyst in the composition is preferably >0.001 to ⁇ 5% by weight, preferably >0.005 to ⁇ 2% by weight, particularly preferably >0.01 to ⁇ 1% by weight, based on the total weight of the two-component Composition.
  • auxiliaries and additives D are paint additives, such as light stabilizers such as UV absorbers and sterically hindered amines (HALS), also stabilizers, defoaming, anti-cratering and/or wetting agents, leveling agents, film-forming auxiliaries, reactive diluents, biocides, solvents or substances for rheology control.
  • light stabilizers in particular UV absorbers such as substituted benzotriazoles, S-phenyltriazines or oxalanilides, and sterically hindered amines, in particular with 2,2,6,6-tetramethylpiperidyl structures—referred to as HALS—is described by way of example in A. Valet , Light stabilizers for paints, Vincentz Verlag, Hanover, 1996.
  • Stabilizers such as radical scavengers and other polymerization inhibitors such as sterically hindered phenols stabilize paint components during storage and are intended to prevent discoloration during curing.
  • Wetting and leveling agents improve surface wetting and/or the leveling of paints. Examples are fluorine surfactants, silicone surfactants and special polyacrylates.
  • Rheology-controlling additives are important in order to control the properties of the two-component system during application and in the leveling phase on the substrate and are known, for example, from patent specifications WO 9422968, EP0276501, EP0249201 or WO 9712945.
  • water scavengers such as triethyl orthoformate, toluene sulfoisocyanate, monooxazolidines or molecular sieves, and hydrolysis inhibitors, such as carbodiimides
  • the proportion of paint additives in the composition is preferably >0.5 to ⁇ 15% by weight, preferably >1 to ⁇ 10% by weight, particularly preferably >2 to ⁇ 7% by weight, based on the total weight of the two-component Composition.
  • a detailed overview of paint additives can be found in the "Textbook of Paints and Coatings, Volume III, Solvents, Plasticizers, Additives, Intermediates", H. Kittel, Verlag W.A. Colomb in Heenemann GmbH, Berlin-Oberschwandorf, 1976, pp. 237-398.
  • Solvents also count as auxiliaries and additives D.
  • the solvent can be an organic solvent or a mixture of organic solvents, or water or a mixture of organic solvent(s) and water.
  • Suitable solvents are to be used in a manner known to the person skilled in the art, matched to the composition and the application method. Solvents should dissolve the components used and promote their mixing and avoid incompatibilities. Furthermore, they should match the coating to the crosslinking reaction taking place during application and curing leave, so that a solvent-free coating with the best possible appearance and without defects such as pops or pinholes is created. Solvents used in two-component technology are particularly suitable.
  • organic solvents examples include ketones such as acetone, methyl ethyl ketone or hexanone, esters such as ethyl acetate, butyl acetate, methoxypropyl acetate, substituted glycols and other ethers, aromatics such as xylene or solvent naphtha such as from Exxon-Chemie, and mixtures of the solvents mentioned.
  • ketones such as acetone, methyl ethyl ketone or hexanone
  • esters such as ethyl acetate, butyl acetate, methoxypropyl acetate, substituted glycols and other ethers, aromatics such as xylene or solvent naphtha such as from Exxon-Chemie, and mixtures of the solvents mentioned.
  • water is also suitable as a solvent or diluent.
  • the proportion of solvent in the composition is preferably >0.5 to ⁇ 40% by weight, preferably >1 to ⁇
  • the process according to the invention is preferably carried out without solvents.
  • the ratio of the polyisocyanate component B to the polyaspartic acid ester-containing component A in the composition, based on the amounts of the polyisocyanate groups to the NCO-reactive groups, is preferably from 0.5:1.0 to 3.0:1.0.
  • a ratio of from 0.9:1.0 to 1.5:1.0 is particularly preferred.
  • a ratio of from 1.05:1.0 to 1.25:1.0 is very particularly preferred.
  • the two-component composition according to the invention is preferably not a foamable or foam-forming composition.
  • the composition is preferably not free-radically polymerizable, in particular not photo-polymerizable, i.e. the composition does not cure by free-radical processes, in particular not by free-radical polymerization processes initiated by actinic radiation.
  • the two-component coating composition according to the invention is produced by methods known per se in the technology of paints and coatings.
  • An isocyanate-reactive component (R) and an isocyanate-containing component (H) are first prepared separately by mixing the respective isocyanate-reactive components A and C, or by mixing the respective polyisocyanate components B.
  • the auxiliaries and additives D are preferably added to the isocyanate-reactive component R.
  • the components R and H produced in this way are only mixed immediately before or during application. If the mixing takes place before application, it should be noted that the reaction of the components already starts after mixing. Depending on the selection of the components and the additives, the reaction will take place at different speeds.
  • the processing time within which the composition must be applied also referred to as pot life and defined as the time from mixing the components until the initial viscosity and/or flow time doubles (determined according to DIN EN ISO 2431:2012-03, but using a DIN 4 flow cup), Depending on the selection of the components, this is then in the range from 1 minute to 24 hours, mostly in the range from 10 minutes to 8 hours.
  • pot life is determined by methods known to those skilled in the art.
  • the invention also relates to a method for coating a substrate, which comprises at least the following steps: i) applying the two-component coating composition described above to at least part of a substrate to be coated, and ii) curing the coating composition from step i).
  • the substrates can already be completely or partially coated with one or more layers of lacquer. These paint layers can still be uncured or moist, partially cured or fully cured; the other paint layers on the substrate are preferably partially cured or fully cured.
  • coats of paint are primers, primers, fillers, fillers, base coats or substrates that have already been completely painted, which are coated again after any pre-treatment such as sanding or plasma activation.
  • the two-component coating compositions are used in particular for producing protective coatings in the construction and wind energy sectors.
  • the use for roof coating, for floor coating and for coating rotor blades in wind turbines, or their leading edges, is mentioned as an example
  • the coating composition can be applied by conventional application methods. Examples of application methods are brushing, brushing, squeegeeing, rolling and spraying, spray or roller application is preferred.
  • the application is followed by an optional curing or drying of the composition according to the invention on the substrate or object. This is done using the methods customary in coating technology, either under ambient conditions with regard to temperature and humidity or under forced conditions, for example by increasing the temperature in ovens, using radiation such as infrared or near-infrared or microwave radiation, and using dehumidified and/or heated air or others gases. It is preferable to dispense with the use of devices for forced curing.
  • the applied coating composition is cured, for example, at temperatures from -20 to 100°C, preferably from -10 to 80°C, more preferably from 0 to 60°C and most preferably from 10 to 40°C. Although not preferred, lower cure temperatures can also be used but will result in longer cure times.
  • compositions are also possible, although not preferred, to cure the composition at higher temperatures, e.g. 80 to 160°C or higher.
  • coatings are obtainable with an elongation at break determined according to DIN EN ISO 527 at 23 ° C and a relative humidity of 50% of preferably at least 8.6 MPa, more preferably at least 10 MPa, most preferably at least 15 MPA and with a Tear propagation resistance determined according to DIN ISO 34-1 at 23° C. and a relative atmospheric humidity of 50% of preferably at least 7 N/mm, particularly preferably at least 10 N/mm, very particularly preferably at least 15 N/mm.
  • Fumaric acid diethyl ester contents were determined quantitatively using a GC method with an internal standard.
  • An Agilent 6890 gas chromatograph with a standard GC capillary (100% polysiloxane phase) and an FID detector was used.
  • the temperature of the injector (split outlet) was 180° C., and helium was used as the carrier gas.
  • the limit of quantification of this method was 200 ppm.
  • the tensile strength and the elongation at break were determined according to DIN EN ISO 527.
  • the tear propagation resistance was determined according to DIN ISO 34-1.
  • Desmophen® NH 1420 commercially available polyaspartic acid ester from Covestro. Characteristics:
  • Desmophen® NH 1423 LF commercially available polyaspartic acid ester from Covestro. Characteristics:
  • Desmophen® NH 1720 commercially available polyaspartic acid ester from Covestro. Characteristics:
  • Desmophen® NH 1723 LF commercially available polyaspartic acid ester from Covestro. Characteristics:
  • Desmophen® NH 1420 commercially available polyaspartic acid ester from Covestro.
  • Desmophen® NH 1420 commercially available polyaspartic acid ester from Covestro.
  • Desmophen® NH 1720 commercially available polyaspartic acid ester from Covestro.
  • Desmophen® NH 1720 commercially available polyaspartic acid ester from Covestro.
  • PAS 1, 5 and 6, or PAS 3, 7 and 8 are based on different degrees of ripeness.
  • Desmodur® N3900 commercially available polyisocyanate from Covestro.
  • Desmodur® E 30700 commercially available polyisocyanate from Covestro.
  • the coatings were produced at room temperature by placing the constituents of component A and component B in a beaker (speed mixer beaker) and homogenizing them at about 2100 rpm for about 30 seconds.
  • the coatings used were applied to a polypropylene plate using the application described and at 23° C./50% rel. humidity networked. For the tests, approx. 1mm thick coatings were produced by casting. The coatings were first stored at room temperature for one day and then stored at 50° C. for 3 days. After
  • test specimens were produced by means of a punch.
  • FSDEE fumaric acid diethyl ester content
  • coatings obtained from coating compositions according to the invention with a fumaric acid diethyl ester content of ⁇ 1.5% by weight have a significantly higher tensile strength (Examples 1 to 4) and in some cases also a significantly higher tear resistance (Examples 1, 3 and 4) as coatings which were produced on the basis of conventional polyaspartic acid esters (Examples 5 to 8).

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  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Wood Science & Technology (AREA)
  • Polyurethanes Or Polyureas (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

Abstract

La présente invention concerne des systèmes de revêtement à deux composants contenant des esters d'acide polyaspartique avec seulement de petites quantités d'esters dialkyliques d'acide fumarique, un procédé de préparation de ceux-ci et leur utilisation pour produire des revêtements destinés à être utilisés dans la construction et l'énergie éolienne. Un exemple pour l'utilisation de ces systèmes est le revêtement de toits, pour le revêtement de planchers et pour le revêtement de pales de rotor d'éoliennes, ou les bords d'attaque de leurs pales de rotor.
EP22765763.2A 2021-08-17 2022-08-12 Nouveaux systèmes de revêtement à deux composants contenant des esters d'acide polyaspartique Pending EP4388025A1 (fr)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
EP21191597.0A EP4137524A1 (fr) 2021-08-17 2021-08-17 Nouveaux systèmes de revêtement à deux composants contenant des esters d'acide polyasparagique
PCT/EP2022/072667 WO2023020960A1 (fr) 2021-08-17 2022-08-12 Nouveaux systèmes de revêtement à deux composants contenant des esters d'acide polyaspartique

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EP22765763.2A Pending EP4388025A1 (fr) 2021-08-17 2022-08-12 Nouveaux systèmes de revêtement à deux composants contenant des esters d'acide polyaspartique

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Family Cites Families (24)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0249201A3 (fr) 1986-06-10 1989-07-19 Union Carbide Corporation Revêtement à base d'époxyde cycloaliphatique résistant à l'affaissement, ayant une haute teneur en matières solides qui contient un polymère à bas poids moléculaire et à haute Tg comme additif résistant à l'affaissement
NO170944C (no) 1987-01-24 1992-12-30 Akzo Nv Fortykkede, vandige preparater, samt anvendelse av slike
DE59007601D1 (de) 1989-06-23 1994-12-08 Bayer Ag Verfahren zur Herstellung von Überzügen.
DE4025347A1 (de) 1990-08-10 1992-02-13 Bayer Ag Verwendung von zweikomponenten-bindemittelkombinationen in autoreparaturlacken
US5214086A (en) 1991-09-04 1993-05-25 Basf Corporation Coating compositions which may be ambient cured
US5243012A (en) 1992-06-10 1993-09-07 Miles Inc. Polyurea coating compositions having improved pot lives
DE4237468A1 (de) 1992-11-06 1994-05-11 Bayer Ag Alkoxysilan- und Aminogruppen aufweisende Verbindungen
DE4310413A1 (de) 1993-03-31 1994-10-06 Basf Lacke & Farben Nichtwäßriger Lack und Verfahren zur Herstellung einer zweischichtigen Decklackierung
DE4327853A1 (de) 1993-08-19 1995-02-23 Bayer Ag Verfahren zur Herstellung von Überzügen
EP0667362A1 (fr) 1994-02-09 1995-08-16 Bayer Corporation Compositions de polyurée pour revêtement à entreposage prolongé
DE4415778A1 (de) 1994-05-05 1995-11-09 Bayer Ag Verfahren zur Herstellung von Überzügen
US5489704A (en) 1994-08-29 1996-02-06 Bayer Corporation Polyisocyanate/polyamine mixtures and their use for the production of polyurea coatings
AU7390296A (en) 1995-10-06 1997-04-28 Cabot Corporation Aqueous thixotropes for waterborne systems
DE19701835A1 (de) 1997-01-21 1998-07-23 Huels Chemische Werke Ag Kalthärtende, lösemittelarme oder lösemittelfreie Zweikomponenten-Polyurethan-Polyharnstoff-Massen
DE19731540A1 (de) 1997-07-23 1999-01-28 Herberts Gmbh Überzugsmittel und deren Verwendung bei Verfahren zur Mehrschichtlackierung
GB0329272D0 (en) 2003-12-18 2004-01-21 Johnson Matthey Plc Catalyst and method of making polyurethane materials
US10125290B2 (en) 2014-02-25 2018-11-13 Axalta Coating Systems Ip Co., Llc Coating compositions comprising diisocyanate chain extended bisaspartates
CN106029728B (zh) 2014-02-25 2019-08-06 涂层国外知识产权有限公司 包含二异氰酸酯扩链的二天冬氨酸酯的涂料组合物
EP3456755A1 (fr) 2017-09-19 2019-03-20 Covestro Deutschland AG Compositions d'esters polyaspartiques contenant des esters polyaspartiques contenant des groupes amine primaires et faibles quantités d'ester dialcoylique d'acide fumarique
EP3456706A1 (fr) 2017-09-19 2019-03-20 Covestro Deutschland AG Compositions d'esters d'acide polyaspartique et procédé de nettoyage
EP3699218A1 (fr) 2019-02-22 2020-08-26 Covestro Deutschland AG Nouveaux systèmes de revêtement de plafond bicomposants contenant des esters d'acide polyaspartique
CN113412295B (zh) 2019-02-22 2023-08-25 科思创知识产权两合公司 包含多天冬氨酸酯的新型双组分清漆体系
PL3990553T3 (pl) * 2019-06-28 2023-10-23 Hempel A/S Zastosowanie kompozycji powlekających do łopat turbin wiatrowych
US20210179903A1 (en) * 2019-12-11 2021-06-17 Covestro Llc Adhesive produced using aspartate-terminated prepolymers

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