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
  • C08G59/00—Polycondensates containing more than one epoxy group per molecule; Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups
  • C08G59/18—Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups ; e.g. general methods of curing
  • C08G59/40—Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups ; e.g. general methods of curing characterised by the curing agents used
  • C08G59/50—Amines
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
  • C08L63/00—Compositions of epoxy resins; Compositions of derivatives of epoxy resins
• • 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
  • C09D163/00—Coating compositions based on epoxy resins; Coating compositions based on derivatives of epoxy resins
• • C—CHEMISTRY; METALLURGY
  • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
  • C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
  • C09J163/00—Adhesives based on epoxy resins; Adhesives based on derivatives of epoxy resins
• • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
  • Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
  • Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
  • Y10T428/00—Stock material or miscellaneous articles
  • Y10T428/31504—Composite [nonstructural laminate]
  • Y10T428/31511—Of epoxy ether

Definitions

• the present invention is directed to methods of benzylation and benzylated compositions from polyamines for curing epoxy resin.
• U.S. Patent No. 7,396,902 B2 which is hereby incorporated by reference in its entirety, discloses a curing agent for epoxy resin that is produced from styrenation of meta xylylene diamine or 1 ,3-BAC (1 ,3-bis(aminomethyl)cyclohexane.
• the 7,396,902 Patent suffers from the drawback that the styrenation process is complicated and arduous.
• U.S. Patent No. 3,634,316 which is hereby incorporated by reference in its entirety, discloses a method for forming antiozonant xylylenediamine derwative. The method includes dehydrohalogenationof halogenated alkyls with xylylenediamine.
• An exemplary relevant claim is claim 2, where an antiozonant is claimed that is ⁇ , ⁇ '- dibenzyl-m, and p-xylylenediamine.
• the product from the 3,634,316 Patent for example, in claim 2, is a dibenzylated product, the manufacture of which is not specified.
• the 3,634,316 Patent does not disclose the formed compounds use in crosslinking agents to crosslink and harden epoxy resins.
• the 3,634,316 Patent does not disclose or provide a method in which the properties are adjustable or tailorable.
• the present disclosure includes a curing agent composition.
• the curing agent composition includes at least one benzylated polyamine compound.
• the benzylated polyamine compound is a reaction product of a benzaidehyde compound or benzyl halide compound and a polyamine according to the following formula:
• A is a phenylene group or a cyclohexylene group.
• the present disclosure includes a method for forming a curing agent composition.
• the method includes contacting a benzaidehyde compound or benzyl halide compound and a polyamine compound according to the following formula:
• A is a phenylene group or a cyclohexylene group.
• the benzaidehyde compound or benzyl halide compound is reacted with the polyamine compound under conditions sufficient to form a benzylated polyamine compound.
• the present disclosure includes an amine- epoxy composition.
• the amine-epoxy composition includes the contact product of a curing agent composition including at least one benzylated polyamine compound, the benzylated polyamine compound being a reaction product of a benzaidehyde compound or benzyl halide compound and a polyamine according to the following formula:
• A is a phenylene group or a cyclohexylene group; and an epoxy composition comprising at least one multifunctional epoxy resin.
• Epoxy curing agents have a low viscosity, a good miscibility with the resin and develops desirable properties when utilized as a crosslinker for epoxy resin.
• Curing agent compositions can maintain single phase uniformity for extended periods of time, which can be required for storage of the product and its subsequent use in its intended application. Additional ⁇ , if these compositions are substantially free of solvents, they can have substantially no VOCs, which can be beneficial for environmental, health and safety issues, as will be appreciated by those skilled in the art.
• Embodiments of the present disclosure diminish the amount of carbamation in a cured system, particularly when the cured system is in the presence of high humidity.
• the epoxy curing agents according to the present disclosure, provide at or about 100% cure, at room temperature, reducing or eliminating the need for the use of benzyl alcohol or other similar compounds to overcome the B stage cure.
• the epoxy curing agents according to the present disclosure, provide a desirably slow cure.
• the method according to the present disclosure, is a simpler process which delivers curing agents for epoxy resin, having good compatibility with the resin.
• embodiments of the present disclosure result in components that are mixable with other amines for easy formulation.
• Embodiments of the present disclosure include epoxy curing agents that result in a percentage of epoxy conversion and crosslinking, including conversion rates of 95-98% or more.
• EPIKOTE® 828 EPON® 8278
• liquid epoxy resin with EEW approximately 184 -192 EPIKOTE® and EPON® are registered trademarks of Momentive Specialty Chemicals Inc., New Jersey.
• IPDA - isophoronediamine, AHEW 43
• the term "contact product”, as utilized herein, describes compositions wherein the components are contacted together in any order, in any manner, and for any length of time.
• the components can be contacted by blending or mixing.
• contacting of any component can occur in the presence or absence of any other component of the compositions or formulations described herein.
• two or more of the components of the contact product may react to form other components composing the composition. Combining additional materials or components can be done by any method known to one of skill in the art.
• Embodiments of the present disclosure include curing agent compositions and methods of making such compositions. These curing agent compositions can be used to cure, harden, and/or crosslink an epoxy resin.
• One embodiment includes curing agent compositions comprising at least one benzylated polyamine compound, the benzylated polyamine compound being a reaction product of a benzaldehyde compound or a benzyl halide compound and a polyamine according to the following formula:
• the benzylated compounds include the reaction product of the reductive amination of a benzaldehyde compound with a diamine of formula (I).
• the benzylated polyamine compounds include the reaction product of a benzyl halide with a polyamine of formula (I).
• the at least one of the polyamines from formula (I) have been benzylated.
• curing agent compositions according to embodiments of the present disclosure, have an amine hydrogen equ ' valent weight (AHEW) based on 100% solids from about 40 to about 200 or about 75 to about 150.
• the curing agent composition comprises a benzylated polyamine of formula (I) component comprising polyamine molecules having one, or two, or three, or four benzyl groups, or any combination thereof.
• benzylated polyamine of formula (I) component for the present invention comprises at least 20 wt% benzylated polyamine of formula (I) having at least two benzyl groups, i.e., having two or more benzyl groups.
• the benzylated polyamine of formula (I) component comprises 20 to 90 wt%, especially 30 to 80 wt%, benzylated polyamine of formula (I) having at leasttwo benzyl groups.
• this curing agent composition has an amine hydrogen equivalent weight (AHEW) based on 100% solids from about 50 to about 160.
• the curing agent composition has an AHEW based on 100% solids from about 80 to about 120.
• the curing agent composition can have an AHEW based on 100% solids from about 30 to about 100.
• the preferred embodiment comprises a benzylated polyamine of formula (I).
• the present invention provides a curing agent composition comprising the contact product of (i) at least one benzylated polyamine compound and (ii) at least one multifunctional amine having three or more active amine hydrogens.
• the at least one benzylated polyamine compound has the formula:
• RA is a substituted or unsubstituted benzyl group
• RB, RC, and RD are independently RA or a hydrogen atom
• A is a phenylene group or a cyclohexylene group, provided that the benzylated polyamine of formula (I) has more than two active amine hydrogen atoms.
• RA and RC are benzyl or vanillyl, or preferably benzyl.
• A is phenylene.
• the benzylated polyamine of formula (I) compound is of the above formula (II), wherein R A is benzyl or vanillyl; R B , R c , and R D are hydrogen atoms.
• R A and R c are benzyl or vanillyl, especially benzyl, and R B and R D are hydrogen atoms.
• A is phenylene.
• benzaldehyde compound or from the reaction with a benzyl halide is necessarily a mixture of many different species, where some of the R B , R c and R D groups are hydrogen and others are benzyl groups. Which and how many of the "R" groups are converted from hydrogen to benzyl groups depends on many factors, among those being the reaction conditions, catalyst selection, reactants ratio, choice of reactant (specific halide compound or benzaldehyde compound), and the like.
• the major component of the reaction product is where is benzyl, R c is benzyl or a hydrogen atom, and R B and R D are hydrogen atoms.
• curing agent compositions described herein can be solvent-based.
• these compositions can further comprise at least one diluent, such as, for example, an organic solvent, or an organic or inorganic acid.
• diluent such as, for example, an organic solvent, or an organic or inorganic acid.
• organic solvent are well known to those skilled in the art of amine formulation chemistry.
• Exemplary organic solvents suitable for use in the present invention include, but are not limited to, benzyl alcohol, butanol, toluene, xylene, methyl ethyl ketone, and the like, or combinations thereof.
• Non-limiting examples of organic and inorganic acids are acetic acid, sulfamic acid, lactic acid, salicylic acid, sebacic acid, boric acid, phosphoric acid, and the like, or combinations thereof. Such acids can increase the curing speed of the curing agent composition.
• the curing agent compositions also can be further modified with monofunctional epoxides, such as, for example, phenyl glycidyl ether, o-cresyl glycidyl ether, p-tert-butyl phenyl glycidyl ether, n-butyl glycidyl ether, and other similar glycidyl ethers or esters.
• curing agent compositions disclosed herein can be blended with other commercially available curing agents.
• Such commercially available curing agenfe include, but are not limited to, solvent based, solvent free or water-based curing agents, which can be employed in a blend to target specific properties, such as cure rate, drying speed, hardness development, clarity, and gloss.
• the method for forming the benzylated polyamine compound includes addition of an aliphatic polyamine represented by formula (I) and benzaldehyde followed by a reduction with H 2 in presence of a catalyst, such as a Pd/C catalyst.
• the benzylated polyamine of formula (I) of the present invention can be prepared by the reductive amination of at least one polyamine of formula (I) compound with the benzaldehyde compound. Procedures for the reductive amination of benzaldehyde are generally known to those of skill in the art. Generally, these procedures involve condensing the benzaldehyde with the amine, then reducing the intermediate Schiff base.
• benzylated mXDA is prepared by reacting mXDA with benzaldehyde, followed by reduction of the system in presence of a suitable catalyst.
• the benzylation of mXDA was carried out at a value of less than two mole benzyldehyde per mole mXDA, preferably 1.2 to 1.3 mole benzaldehyde per mole of amine, therefore having a product with a small amount of free amine.
• the molar reactant ratio of the benzaldehyde compound to the at least one polyamine of formula (I) compound is in a range from about 0.8:1 to about 1.98:1.
• the molar reactant ratio of the benzaldehyde compound to the at least one polyamine of formula (I) compound is about 0.9:1 , about 1 :1 , about 1.1 :1 , about 1.2:1 , about 1.3:1 , about 1.4: 1 , about 1.5:1 , about 1.6:1 , about 1.7:1 , about 1.8:1 , or about 1.9:1.
• the molar reactant ratio is in a range from about 0.9:1 to about 1.8:1 , or from about 1 :1 to about 1.6:1.
• the molar reactant ratio of the benzaldehyde compound to the at least one polyamine of formula (I) compound is in a range from about 1.2:1 to about 1.5:1.
• the product should retain more than two reactive amine hydrogen, to allow a proper cross- linking of the epoxy resin. Even at molar reactant ratios of the benzaldehyde compound to the at least one polyamine of formula (I) compound, less than 1 :1 dibenzylated aminopropylatedalkylenediamine APADAs are produced in minor amounts.
• molar reactant ratios of the benzaldehyde compound to the at least one polyamine of formula (I) compound of 1 :1 to 1.6:1 is preferably used.
• the benzylated polyamine of formula (I) of the present disclosure can also be prepared by the reaction of at least one polyamine of formula (I) compound with a benzyl halide.
• molar reactant ratios of the at least one benzyl halide compound to the at least one APADA compound are within a range from about 0.8:1 to about 2:1.
• the molar reactant ratio is about 0.9:1 , about 1 :1 , about 1.1 :1 , about 1.2:1 , about 1.3:1 , about 1.4:1 , about 1.5:1 , about 1.6:1 , about 1.7:1 , about 1.8:1 , or about 1.9:1.
• the molar reactant ratio of the at least one benzyl halide to the at least one polyamine of formula (I) compound is in a range from about 1.2:1 to about 1.5:1.
• the curing agent composition comprises a benzyiated polyamine of formula (I) component comprising polyamine molecules having one, or two, or three, or four benzyl groups, or any combination thereof.
• benzyiated poiyamines of formula (I) component for the present invention comprise at least 20 wt% benzyiated poiyamines of formula (I) having at least two benzyl groups, i.e., having two or more benzyl groups.
• the benzyiated poiyamines of formula (I) component comprise 20 to 90 wt%, especially 30 to 80 wt%, benzyiated poiyamines of formula (I) having at least two benzyl groups.
• the curing agent composition in this aspect of the present invention, can have an AHEW based on 100% solids from about 50 to about 160. Further, such curing agent composition can have an AHEW based on 100% solids in the range from about 80 to about 120. In a different aspect, the curing agent composition has an AHEW based on 100% solids from about 30 to about 100.
• the preferred embodiment comprises benzyiated poiyamines of formula (I).
• the curing agent composition comprises a benzyiated poiyamines of formula (I) component comprising polyamine molecules having one, or two, or three, or four alkyl groups or any combination thereof.
• benzyiated poiyamines of formula (I) component for the present invention comprise at least 20 wt% benzyiated poiyamines of formula (I) having one or more benzyl groups, preferably 20 to 90 wt%, especially 30 to 80 wt% poiyamines of formula (I) having one or more benzyl groups.
• an amine-epoxy composition in accadance with the present disclosure, includes the reaction product of A) at least one benzyiated polyamine compound; and B) an epoxy composition comprising at least one multifunctional epoxy resin.
• an amine-epoxy composition includes the reaction product of A) a curing agent composition comprising the contact product of (i) at least one benzyiated; and (ii) at least one multifunctional amine having three or more active amine hydrogens; and B) an epoxy composition comprising at least one multifunctional epoxy resin.
• various additives can be present in the compositions or formulations used to produce fabricated articles, dependent upon the desired properties.
• additives can include, but are not limited to, solvents (including water), accelerators, plasticizeis, fillers, fibers such as glass or carbon fibers, pigments, pigment dispersing agents, rheology modifiers, thixotropes, flow or leveling aids, surfactants, defoamers, biocides, or any combination thereof.
• polyamine compounds that are useful in producing the benzylated polyamine compounds according to the present disclosure include, but are not limited to, diamines represented by formula (I).
• Other suitable polyamines include
• orthoxylyienediamine metaxylylenediamine, paraxylylenediamine, 1.2- bis(aminomethyl)cyclohexane, 1 ,3-bis (aminomethyl)cyclohexane, 1,4-bis
• Metaxylylenediamine, 1 ,3-bis (aminomethyl)cyclohexane are particularly suitable. These amines can be used individually or mixed with one another.
• the benzylated polyamine compound is a benzylated polyamine, the polyamine having a structure according to formula (I).
• the benzylated amines can be a benzylated orthoxylyienediamine,
• the benzylated amine is a mixture of benzylated polyamine
• Benzaldehyde compounds suitable for use in the benzylation of the polyamines include unsubstituted benzaldehyde and substituted benzaldehydes.
• Suitable substituted benzaldehydes include, but are not limited to, compounds of the formula PhCHO, where Ph is a moiety including an aromatic ring, in which Ph is unsubstituted or substituted with one or more of halogen atoms, Ci-C 4 alkyl, methoxy, ethoxy, amino, hydroxyl or cyano groups.
• the benzaldehyde compound is benzaldehyde and in another embodiment, the benzaldehyde compound is vanilin.
• Benzyl halide compounds suitable for use in the benzylation of the polyamines include benzyl fluoride, benzyl chloride, benzyl bromide or benzyl iodide.
• the benzyl group may comprise unsubstituted benzyl or a substituted benzyl group.
• Substituted benzyl groups include, but are not limited to, radicals of the formula PhCH 2 - , where Ph is a moiety including an aromatic ring, in which Ph is unsubstituted or substituted with one or more of halogen atoms, C C 4 alkyl, methoxy, ethoxy, amino, hydroxyl or cyano groups.
• the benzyl group is benzyl and in another embodiment the benzyl is vanillyl.
• the resultant product has a lower viscosity which allows benzylation to a point where there is little or no free amine is present in the final product. While not wishing to be bound by theory, it is believed that the removal of the free amine helps in reducing the carbamation of the film caused by the reaction of the primary amine in the presence of water and carbon dioxide. The decrease/absence of smoking or fuming; the improved compatibility with epoxy resin; the lower tendency to carbamate; and the low level of free, unreacted amine in the final product result in improved handling properties.
• the polyamines of formula (I) such as metaxylylenediamine
• Curing agent compositions in accordance with the present disclosure can comprise at least one multifunctional amine.
• Multifunctional amine describes compounds with amine functionality and which contain three (3) or more active amine hydrogens.
• Non-limiting examples of multifunctional amines that are within the scope of the present invention include, but are not limited to, an aliphatic amine, a cycloaliphatic amine, an aromatic amine, a poly(alkylene oxide) diamine or triamine, a Mannich base derivative of an aliphatic amine, a cycloaliphalic amine, or an aromatic amine, a polyamide derivative of an aliphatic amine, a cycloaliphaic amine, or an aromatic amine with a dimer fatty acid or a mixture of a dimer fatty acid and fatty acid, an amidoamine derivative of an aliphatic amine, a cycloaliphatic amine, or an aromatic amine with a fatty acid, an amine adduct derivative of an aliphatic amine, a cycloaliphatic amine, or an aromatic amine with a glycidyl ether of bisphenol A or bisphenol F or an epoxy novolac resin, and
• AHEW can be calculated based on its chemical structure, or is often provided by the supplier of the amine in case of a mixture.
• the AHEW for the benzylated polyamines of formula (I) compound, AHEW B is determined using the following formula, assuming the polyamines of formula (I) is the reductive amination product of x moles of benzaldehyde, for example, with 1 mole of a polyamines of formula (I) compound, Forml (the polyamines of formula (I) compound and the benzaldehyde are discussed in greater detail below):
• AHEW MW Fo m . + * ( M W A.d - 1 6 )
• MWForml is the average molecular weight of the polyamines of formula (I);
• MWAId is the molecular weight of the benzaldehyde
• f is the average amine hydrogen functionality of the polyamines of formula (I); and x is the number of moles benzaldehyde used;
• MWBforml is the average molecular weight of Ihe benzylated polyamines of formula (I) and can be calculated as follows:
• MWsforml MWForml + X ⁇ (MW A
• the at least one multifunctional amine can comprise an aliphatic amine and a Mannich base derivative of a cycloaliphalic amine.
• the at least one multifunctional amine can comprise one aliphatic amine and one different aliphatic amine.
• Exemplary aliphatic amines include polyethyleneamines (EDA, DETA, TETA, TEPA, PEHA, and the like), polypropyleneamines, aminopropylated ethylenediamines (Am3, Am4, Am5, and the like), aminopropylated propylenediamines, 1 ,6- hexanediamine, 3,3,5-trimethyl-l ,6-hexanediamine, 3,5,5-trimethyM ,6-hexanediamine, 2-methyl-1 ,5-pentanediamine, and the like, or combinations thereof.
• EDA polyethyleneamines
• DETA DETA
• TETA TETA
• TEPA TEPA
• PEHA polypropyleneamines
• aminopropylated ethylenediamines Am3, Am4, Am5, and the like
• aminopropylated propylenediamines 1 ,6- hexanediamine, 3,3,5-trimethyl-l ,6-hexanediamine, 3,5,5-trime
• the at least one multifunctional amine is EDA, DETA, TETA, TEPA, PEHA, propylenediamine, dipropylenetriamine, tripropylenetetramine, Am3, Am4, Am5, N-3- aminopropyM ,3-diaminopropane, N,N'-bis(3-aminopropyl)-1 ,3-diaminopropane, ⁇ , ⁇ , ⁇ '- tris(3-aminopropyl)-1 ,3-diaminopropane, or any combination thereof.
• the poly(alkylene oxide) diamines and triamines commercially available underthe
• JEFFAMINE ® trademark from Huntsman Corporation are useful in the present invention. Illustrative examples include, but are not limited to, JEFFAMINE D-230, JEFFAMINE D-400, JEFFAMINE ® D-2000, JEFFAMINE ® D-4000, JEFFAMINE ® T-403, JEFFAMINE ® EDR-148, JEFFAMINE ® EDR-192, JEFFAMINE ® C-346, JEFFAMINE ® ED-600, JEFFAMINE ® ED-900, JEFFAMINE ® ED-2001 , and the like, or combinations thereof.
• JEFFAMINE ® is a registered trademark of Huntsman Petrochemical LLC.
• Cycloaliphatic and aromatic amines include, but are not limited to, 1 ,2- diaminocyclohexane, 1 ,3-diaminocyclohexane, 1 ,4-diaminocyclohexane, hydrogenated orf/70-toluenediamine, hydrogenated mefa-toluenediamine, metaxylylene diamine, hydrogenated mefaxylylene diamine (referred to commercially as 1 ,3-BAC), isophorone diamine, norbornane diamines, 3,3'-dimethyl-4,4'-diaminodicyclohexyl methane, 4,4'- diaminodicyclohexyl methane, 2,4'-diaminodicyclohexyl methane, a mixture of methylene bridged poly(cyclohexyl-aromatic)amines, and the like, or combinations thereof.
• the mixture of methylene bridged poly(cyclohexyl-aromatic)amines is abbreviated as either MBPCAA or MPCA, and is described in U.S. Patent Number 5,280,091 , which is incorporated herein by reference in its entirety.
• the at least one multifunctional amine is a mixture of methylene bridged poly(cyclohexyl- aromatic)amines (MPCA).
• Mannich base derivatives can be made by the reaction of the above described aliphatic amines, cycloaliphatic amines, or aromatic amines with phenol or a substituted phenol and formaldehyde.
• An exemplary substituted phenol used to make Mannich bases with utility in the present invention is cardanoi, which is obtained from cashew nut shell liquid.
• Mannich bases can be prepared by an exchange reaction of a multifunctional amine with a tertiary amine containing a Mannich base, such as tris- dimethylaminomethylphenol (commercially available as ANCAMINE ® K-54 from Air Products and Chemicals, Inc.) or Jb/s-dimethylaminomethylphenol.
• Polyamide derivatives can be prepared by the reaction of an aliphatic amine, cycloaliphatic amine, or aromatic amine with dimer fatty acid, or mixtures of a dimer fatty acid and a fatty acid.
• Amidoamine derivatives can be prepared by the reaction of an aliphatic amine, cycloaliphatic amine, or aromatic amine with fatty acids.
• Amine adducts can be prepared by the reaction of an aliphatic amine, cycloaliphatic amine, or aromatic amine with an epoxy resin, for example, with the diglycidyl ether of bisphenol-A, the diglycidyl ether of bisphenol-F, or epoxy novolac resins.
• Amine-epoxy compositions of the present invention comprise the reactbn product of a curing agent composition and an epoxy composition comprising at least one multifunctional epoxy resin.
• Multifunctional epoxy resin as used herein, describes compounds containing 2 or more 1 ,2-epoxy groups per molecule. Epoxide compounds of this type are well known to those of skill in the art and are described in Y. Tanaka,
• the relative amount chosen for the epoxy composition versus that of the curing agent composition, or hardener can vary depending upon, for example, the end-use article, its desired properties, and the fabrication method and conditions used to produce the end-use article. For instance, in coating applications using certain amine-epoxy compositions, incorporating more epoxy resin relative to the amount of the curing agent composition, can result in coatings which have hcreased drying time, but with increased hardness and improved appearance as measured by gloss.
• Amine-epoxy compositions of the present invention generally have stoichiometric ratios of epoxy groups in the epoxy composition to amine hydrogens in the curing agent composition ranging from about 1.5:1 to about 0.7:1. For example, such amine-epoxy compositions can have
• stoichiometric ratios of about 1.5:1 , about 1.4:1 , about 1.3:1 , about 1.2:1 , about 1.1 :1 , about 1 :1 , about 0.9:1 , about 0.8:1 , or about 0.7:1.
• the stoichiometric ratio ranges from about 1.3:1 to about 0.7:1.
• the stoichiometric ratio ranges from about 1.2:1 to about 0.8:1.
• the stoichiometric ratio ranges from about 1.1 :1 to about 0.9:1.
• One class of epoxy resins suitable for use in the present invention comprises the glycidyl ethers of polyhydric phenols, including the glycidyl ethers of dihydric phenols.
• Illustrative examples include, but are not limited to, the glycidyl ethers of resorcinol, hydroquinone, bis-(4-hydroxy-3,5-difluorophenyl)-methane, 1 ,1-bis-(4-hydroxyphenyl)- ethane, 2,2-bis-(4-hydroxy-3-methylphenyl)-propane, 2,2-bis-(4-hydroxy-3,5- dichlorophenyi) propane, 2,2-bis-(4-hydroxyphenyl)-propane (commercially known as bisphenol A), bis-(4-hydroxyphenyl)-methane (commercially known as bisphenol F, and which may contain varying amounts of 2-hydroxyphenyl isomers), and the like, or any combination thereof.
• m is an integer
• R is a divalent hydrocarbon radical of a dihydric phenol, such as those dihydric phenols listed above.
• Materials according to this formula can be prepared by polymerizing mixtures of a dihydric phenol and epichlorohydrh, or by advancing a mixture of a diglycidyl ether of dihydric phenol. While in any given molecule the value of m is an integer, the materials are invariably mixtures which can be characterized by an average value of m, which is not necessarily a whole number. Polymeric materials with an average value of m between 0 and about ? can be used in one aspect of the present invention.
• epoxy novolac resins which are the glycidyl ethers of novolac resins
• the at least one multifunctional epoxy resin is a diglycidyl ether of bisphenol-A (DGEBA), an advanced or higher molecular weight version of DGEBA, a diglycidyl ether of bisphenokF, an epoxy novolac resin, or any combination thereof.
• DGEBA diglycidyl ether of bisphenol-A
• EW epoxy equivalent weights
• DGEBA or advanced DGEBA resins are often used in coating formulations due to a combination of their low cost and generally high performance properties.
• DGEBA Commercial grades of DGEBA having an EEW ranging from about 174 to about 250, and more commonly from about 185 to about 195, are readily available. At these low molecular weights, the epoxy resins are iquids and are often referred to as liquid epoxy resins. It is understood by those skilled in the art that most grades of liquid epoxy resin are slightly polymeric, since pure DGEBA has an EEW of 174. Resins with EEW's between 250 and 450, also generally prepared by the advancement process, are referred to as semi-solid epoxy resins because they are a mixture of solid and liquid at room temperature. Generally, multifunctional resins with EEW's based on solids of about 160 to about 750 are useful in the prevent invention. In another aspectthe
• multifunctional epoxy resin has an EEW in a range from about 170 to about 250.
• the viscosity of the compositions of the present invention can be reduced to allow an increase in the level of pigment in a formulation or composition while still permitting easy application, or to allow the use of a higher molecular weight epoxy resin.
• the epoxy component which comprises at least one multifunctional epoxy resin, to further comprise a monofunctional epoxide.
• monoepoxides include, but are not limited to, styrene oxide, cyclohexene oxide, ethylene oxide, propylene oxide, butylene oxide, and the glycidy!
• the multifunctional epoxy resin can also be present in a solution or emulsion, with the diluent being water, an organic solvent, or a mixture thereof.
• compositions of the present invention can be used to produce various articles of manufacture.
• various additives can be employed in the formulations and compositions to tailor specific properties.
• additives include, but are not limited to, solvents (includingwater), accelerators, plasticizers, fillers, fibers such as glass or carbon fibers, pigments, pigment dispersing agents, rheology modifiers, thixotropes, flow or leveling aids, surfactants, defoamers, biocides, or any combination thereof. It is understood that other mixtures or materials that are known in the art can beincluded in the compositions or formulations and are within the scope of the present invention.
• an article can comprise an amine-epoxy composition which comprises the reaction product of a curing agent composition and an epoxy composition.
• Articles of manufacture produced from amine-epoxy compositions disclosed herein include, but are not limited to, adhesives, coatings, primers, sealants, curing compounds, construction products, flooring products, and composite products. Further, such coatings, primers, sealants, or curing compounds can be applied to metal or cementitious substrates. Coatings based on these amine-epoxy compositions can be solvent-free or can contain diluents, such as water or organic solvents, as needed for the particular appication.
• Coatings can contain various types and levels of pigments for use in paint and primer applications.
• Amine-epoxy coating compositions comprise a layer having a thickness ranging from 40 to 400 pin (micrometer), preferably 80 to 300 pm, more preferably 100 to 250 pm, for use in a protective coating applied on to metal substrates.
• coating compositions for use in a flooring product or a construction product, comprise a layer having a thickness ranging from 50 to 10,000 pm, depending on the pe of product and the required end-properties.
• a coating product that delivers limited mechanical and chemical resistances comprises a layer having a thickness ranging from 50 to 500 pm, preferably 100 to 300 pm; whereas a coating product such as, for example, a self-leveling floor that delivers high mechanical and chemical resistances comprises a layer having a thickness ranging from 1 ,000 to 10,000 pm, preferably 1 ,500 to 5,000 urn.
• substrates are suitable for the applicatbn of coatings of this inventbn with proper surface preparation, as is well known to one of ordinary skill in the art.
• substrates include, but are not limited to, concrete and various types of metals and alloys, such as steel and aluminum.
• Coatings of the present invention are suitable for the painting or coating of large metal objects or cementitious substrates including ships, bridges, industrial plants and equipment, and floors.
• Coatings of this invention can be applied by any number of techniques including spray, brush, roller, paint mitt, and the like.
• plural component spray application equipment can be used, in which the amine and epoxy components are mixed in the lines leading to the spray gun, in the spray gun itself, or by mixing the two components together as they leave the spray gun.
• Heated plural component equipment can be employed to reduce the viscosity of the components, thereby improving ease of application.
• Construction and flooring applications include compositions comprising the amine-epoxy compositions of the present invention in combination with concrete or other materials commonly used in the construction industry.
• Applications of compositions of the present invention include, but are not limited to composition's use as a primer, a deep penelrating primer, a coating, a curing compound, and/or a sealant for new or old concrete, such as referenced in ASTM C309-97, which is incorporated herein by reference.
• a primer or a sealant the amine-epoxy compositions of the present invention can be applied to surfaces to improve adhesive bonding prior to the application of a coating.
• a coating is an agent used for application on a surface to create a protective or decorative layer or a coat. Crack injection and crack filling products also can be prepared from the
• compositions disclosed herein can be mixed with cementitious materials such as concrete mix to form polymer or modified cements, tile grouts, and the like.
• cementitious materials such as concrete mix to form polymer or modified cements, tile grouts, and the like.
• composite products or articles comprising amine-epoxy compositions disclosed herein include tennis rackets, skis, bike frames, airplane wings, glass fiber reinforced composites, and other molded products.
• these curing agent compositions will have applicability in making epoxy filament-wound tanks, infusion composites such as windmill blades, aerospace adhesives, industrial adhesives, as well as other related applications.
• a composite is a material made of different substances, and in the case of resin technologies, composites refer to resin impregnated systems where the resin is reinforced by the addition of reinforcing materials such as fillers and fibers for improving general properties of the resulting product. These materials work together but are not soluble in one another.
• the binder component comprises the epoxy resin and epoxy curing agen3 ⁇ 4s).
• Resin infusion is a process by which resin is introduced to the composite mold, the reinforcement material having already been placed into the mold and closed prior to resin introduction. There are variations on this process such as those that are vacuum assisted.
• An advantage of 1he use of benzylated polyamine of formula (I) in amine-epoxy compositions for making composites is the longer pot life and improved compatibility versus the unmodified polyamines.
• the advantage in adhesives is again longer pot life, in this case, so there is no skin-over before the parts are glued together, which is a major concern for large aircraft and windmill blades, when it takes a long time to place the adhesive beads across the entire part.
• Lower blush due to the benzyl group adds to the lower skin-over.
• the low viscosity allows for high filler levels.
• the benzylated curing agenfe of the invention show good physical properties, comparable to amines like isophoronediamine (IPDA), which are used in composites for mechanical strength and compatibility with epoxy resin (see table below).
• IPDA isophoronediamine
• these benzylated polyamine of formula (I) curing agents are lower Tg than IPDA so do not need as extensive a cure time/temperature in order to fully cure, resulting in lower processing costs.
• IPDA- EPON ® 828 is known to be brittle when it does not fully cure, which is one of the reasons why formulators use high levels of plasticizers (benzyl alcohol) with IPDA in room- temperature cure coatings and why IPDA needs to be fully cured in composite applications.
• epoxy resins which are cured, hardened, and/or crosslinked with amine-based curing agents are well known. These amine-epoxy materials are widely used in applications ranging from coatings, where they can be used in various applications such as primers, tie-coats, and finishes. They can be applied on many substrates. They can be used in laminates, adhesives, floorings, dust free finishes, secondary containment, linings, reinforcement, repair formulations, tooling, potting, and casting.
• curing agents for epoxy resins they can be used in a wide range of applicatbns such as coatings, where they can be used in various applicafons such as primers, tie-coats, and finishes. They can be applied on many substrates. They can be used in laminates, adhesives, floorings, dust free finishes, secondary containment, linings, reinforcement, repair formulations, tooling, potting, and casting.
• the present invention also includes articles of manufacture comprising an amine-epoxy composition as described above.
• articles can include, but are not limited to, an adhesive, a coating, a primer, a sealant, a curing compound, a construction product, a flooring product, a composite product, laminate, potting compounds, grouts, fillers, cementitious grouts, or self-leveling flooring. Additional components or additives can be used together with the compositions of the present invention to produce articles of manufacture. Further, such coatings, primers, sealants, curing compounds or grouts can be applied to metal or cementitious substrates.
• Example 1 Synthesis of benzylated metaxylylenediamine 1.15/1.0 molar ratio.
• benzylated metaxylylenediamine is a one-batch process. 416 g of mXDA (3.06 moles) and 4.2 g of Pd/C catalyst were placed in a 1 -liter autoclave bateh reactor. The reactor was sealed and subsequently purged with nitrogen and then with hydrogen to remove any air from the reactor. Over about 15 to 20 minutes, 372.4 g of benzaldehyde (3.51 moles) were added to the reactor. After the addition of the benzaldehyde was complete, the reactor contents were stirred for an additional 15 minutes or until the reaction was complete, at which time the reaction exotherm began to subside.
• the reactor was pressurized to 8.17 atm (120 psi) with hydrogen and the reactor was heated b 80 °C.
• the pressure was increased to 54.4 atm (800 psi) and the temperature was increased to 120 °C.
• the hydrogenatbn process continued until the rate of hydrogen uptake fell bebw 0.0034 MPaAnin (0.5 psi/min).
• the total hydrogenation time was about 5 hours.
• the reactor was cooled to 60 °C and depressurized, and the reaction product was filtered to remove the catalyst. Water was removed using a rotary-evaporator operating under 20 mm Hg vacuum and temperatures up to 120 °C.
• the resulting reaction product was benzylated mXDA, with viscosity, AHEW and amine value (measured). The properties are shown in Table 1.
• benzylated metaxylylenediamine is a one-batch process. 750 g of mXDA (5.51 moles) and 7.5 g of Pd/C catalyst were placed in a 1 -gallon autoclave batch reactor. The reactor was sealed and subsequently purged with nitrogen and then with hydrogen to remove any air from the reactor. Over about 15 to 20 minutes, 758.6 g of benzaldehyde (7.15 moles) were added to the reactor. After the addition of the benzaldehyde was complete, the reactor contents were stirred for an additional 15 minutes or until the reaction was complete, at which time the reaction exotherm began to subside.
• the reactor was pressurized to 8.17 atm (120 psi) with hydrogen and the reactor was heated b 80 °C.
• the pressure was inaeased to 54.4 atm (800 psi) and the temperature was increased to 120 °C.
• the hydrogenatton process continued until the rate of hydrogen uptake fell bebw 0.0034 MPaAnin (0.5 psi/min).
• the total hydrogenation time was about 5 hours.
• the reactor was cooled to 60 °C and depressurized, and the reaction product was filtered to remove the catalyst. Water was removed using a rotary-evaporator operating under 20 mm Hg vacuum and temperatures up to 120 °C.
• the resulting reaction product was benzylated mXDA, with viscosity, AHEW and amine value (measured). The properties are shown in Table 2.
• Comparative example 3 Synthesis of styrenated metaxylylenediamine at about 1.30/1.0 molar ratio.
• Example 4 summarizes the amine-epoxy compositions used in Examples 4, 5 and 6.
• the composition of Example 4 was 100 g of EPIKOTETM 828 epoxy resin, and 44.2 g of the curing agent composition of Example 1.
• Example 1 was a curing agent composition comprising the reaction product of mXDA with benzaldehyde followed by reductive hydrogenation.
• the curing agents and their respective quantities shown in Examples 4, 5 and 6 were used as per Tables 4 and 5.
• Table 4 shows that benzylation had a slightly favorable influence on the degree of cross-linking of the resin. The Tg was slightly higher. The same brittleness was encountered. Table 4
• Drying times for the amine-epoxy compositions are summarized in Table 5.
• the drying time was determined at 23 °C and 65% relative humidity (RH) using a Beck-Koller recorder, in accordance with ASTM D5895.
• the procedure involved coatingglass panels with the amine-epoxy compositions at approximately 6 mils wet film thickness.
• the selection of a coating composition with either a long or short drying time depends upon the requirements of the end-use application.
• the results in Table 5 indicated that the coatings of inventive Examples 4, 5 and 6 had various drying times depending on the degree of benzylation/styrenation used.
• Table 5 also lists the Persoz Hardness test results after 1 day, 3 days, and 7 days, respectively, at 23 °C and 50% RH. Coatings were applied to glass panels at a wet film thickness of about 8 mils and tested in accordance with ISO 1522. As shown in Table 5, the formulations of inventive Examples 4 and 5 have similar Persoz hardness development to that of the styrenated curing agent. Additionally, the coatings of inventive Examples 4 and 5 had faster hardness development after 24 hours than the styrenated amine example.
• Table 5 lists the 60° Gloss test results after 1 day, 3 days, and 7 days, respectively, at 23 °C and 50% RH. Results shown are the average of 10
• Example 4 has a lower gloss than Example 5 due to the higher content in free amine.
• Example 5 compares favorably with Example 6 with a high gloss value, this is due in both cases to the good miscibility of the curing agent with the resin.
• Example 4 has a lower resistance to blush than Example 5 due to the higher content in free amine.
• Example 5 compares favorably with Example 6 with a high resistance to blush, this is due in both cases to the low free amine value and also the good miscibility of the curing agents with the resin.

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