Patent Application
20110313082
The following disclosure relates to epoxy-based adhesive compositions, in particular epoxy-based adhesive compositions that exhibit high mechanical strength over a wide temperature range. Such adhesives are useful in structural assembly, such as for example as repair materials in motor vehicles or aircrafts. The disclosure also relates to processes of preparing the adhesives and to applications of the adhesives.
Structural adhesives are adhesive compositions that can bond materials with a mechanical strength comparable to mechanical fasteners. They may be used to replace or augment conventional joining techniques such as welding or mechanical fasteners, such as nuts and bolts, screws and rivets etc. In particular in the transportation industries structural adhesives can present a light weight support of or even an alternative to mechanical fasteners.
Epoxy resin compositions have been long known for their good adhesive and mechanical properties and have been widely used as bonding agents. Many of these compositions contain latent curatives (for example dicyandimides, anhydrides or aromatic amines, such as for example diaminodiphenyl sulfone) and require high temperatures for curing the adhesive composition. Such adhesive systems are referred to as “one-component systems”. Other epoxy adhesive formulations with more reactive curing agents can be cured at lower temperatures. Such systems are referred to as “two-component systems”, because at least the majority of the epoxy resins are kept separated from the curing agents to avoid premature cross-linking. The two parts are combined upon application of the adhesive to initiate the curing reaction.
When used as structural adhesives in transportation applications, such as for example, for bonding components or parts in motor vehicles, aircrafts or watercrafts, the epoxy resins are required to maintain their good mechanical properties not only at room temperature but also at elevated temperatures and low temperatures. Preferably, the curing system is also curable at comparatively low temperatures to save costs.
In US2007/0293603A1 a low temperature curable epoxy adhesive composition comprising an epoxy resin containing part (A) and a part (B) comprising a polyamine and a flexible polyamide is reported to have good bonding strength at room temperature and above (73F and 180F). However, when used as structural adhesives good mechanical bonding strength is required over a wider temperature range and including temperatures below freezing. For example, airplanes can be exposed to temperatures as low as −55° C. in high altitudes. Cars may also be exposed to low temperatures in extreme weather conditions in various areas of the world. Parts of an aircraft or a motor vehicle may also be exposed to elevated temperatures. Therefore, there exists a need to provide structural adhesive compositions that have good mechanical strength (in particular good bond strength) at temperatures far below 0° C. and at room temperature and at elevated temperatures.
It has now been found that certain structural adhesive formulations provide good bonding strength over a wide temperature range below and above freezing. Such adhesive formulations can be cured at temperatures as low as 80° C.
In the following there is provided a precursor composition for a curable adhesive, said precursor composition comprising two parts, part (A) and part (B), which are separated from each other,
wherein part (B) comprises the following components:
(i) one or more epoxy resins,
wherein part (A) comprises the following components:
(ii) a combination of at least two curing agents, the first curing agent comprising a cycloaliphatic amine and the second curing agent being different from the first curing agent comprising a linear aliphatic amine,
the precursor composition further comprising either in part (A) or in part (B) or in both (A) and (B)
(iii) a first core-shell polymer toughening agent
(iv) a second core-shell polymer toughening agent
(v) a filler material selected from particles having a particle size from about 0.5 to about 500 μm.
There is also provided an adhesive composition comprising
(i) the reaction product of an epoxy resins with a linear aliphatic amine and a cycloaliphatic amine,
(ii) a first core-shell polymer toughening agent
(iii) a second core-shell polymer toughening agent
(iv) a filler material selected from particles having a particle size from about 0.5 to about 500 μm.
Furthermore there is provided an article comprising the adhesive composition described above.
In another aspect there is provided the use of the adhesive composition described above for bonding components of an airplane or a motor vehicle or for bonding of components to an airplane or a motor vehicle.
In yet another aspect there is provided a process for joining parts comprising combining the two parts of a precursor composition described above form an adhesive composition, applying the adhesive composition to a first substrate, placing the second substrate that is to be joined with first substrate on the adhesive composition and curing the adhesive composition.
In a further aspect there is provided a process of making an adhesive composition comprising
providing a two part precursor composition described above,
combining the two parts of the precursor composition to form an adhesive composition, curing the adhesive composition,
wherein the components of the two parts precursor compositions are present in amounts such that the cured adhesive composition has a peel strength of at least 80 N at −55° C., 23° C. and 90° C. as measured according to DIN 2243-2 (2005) for a bond thickness of 150 μm on an aluminum substrate.
Before any embodiments of this disclosure are explained in detail, it is to be understood that the disclosure is not limited in its application to the details of construction and the arrangement of components set forth in the following description. The invention is capable of other embodiments and of being practiced or of being carried out in various ways. Also, it is to be understood that the phraseology and terminology used herein is for the purpose of description and should not be regarded as limiting. Contrary to the use of “consisting”, the use of “including,” “containing”, “comprising,” or “having” and variations thereof is meant to encompass the items listed thereafter and equivalents thereof as well as additional items. The use of “a” or “an” is meant to encompass “one or more”. Any numerical range recited herein is intended to include all values from the lower value to the upper value of that range. For example, a concentration range of from 1% to 50% is intended to be an abbreviation and to expressly disclose the values between the 1% and 50%, such as, for example, 2%, 40%, 10%, 30%, 1.5%, 3.9% and so forth.
The adhesive formulations described herein are two part precursor formulations which when combined provide a curable adhesive composition. The first part of the precursor composition, part (A), contains curing agents that are capable to cross-link epoxy resins and the second part of the precursor composition, part (B), contains epoxy resins that can be cured by the curing agents of part (A).
The terms “solid” or “liquid” refer to ambient conditions (20° C., 1 bar)
Particle sizes are number averages. In case of particles that are only substantially spherical the particle size is determined by adding the length of the two main (largest orthogonal) axes of the particle and dividing it by two. “Substantially spherical” means one or all main axes (x-,y- or z-axis) may deviate from the required length to form a perfect sphere by up to 50%, preferably up to 25%.
Epoxy resins are polymers having one or more epoxy-functionality. Typically but not exclusively, the polymers contain repeating units derived from monomers having an epoxy-functionality but epoxy resins can also include, for example, silicone-based polymers that contain epoxy groups or organic polymer particles coated with or modified with epoxy groups or particles coated with, dispersed in, or modified with epoxy-groups-containing polymers. The epoxy-functionalities allow the resin to undertake cross-linking reactions. The epoxy resins may have an average epoxy-functionality of at least 1, greater than one, or of at least 2.
Epoxy resins may be aromatic, aliphatic, cycloaliphatic or mixtures thereof. Preferably, the epoxy resins contain moieties of the glycidyl or polyglycidyl ether type. Such moieties may be obtained, for example, by the reaction of a hydroxyl functionality (for example but not limited to dihydric or polyhydric phenols or aliphatic alcohols including polyols) with an epichlorohydrin-functionality. As referred to herein, dihydric phenols are phenols containing at least two hydroxy groups bonded to the aromatic ring (also referred to as “aromatic” hydroxy groups) of a phenol or in case of polyphenols at least two hydroxy groups are bonded to an aromatic ring. This means the hydroxyl groups can be bonded to the same ring of the polyphenol or to different rings each of the polyphenol. Therefore, the term “dihydric phenols” is not limited to phenols or polyphenols containing two “aromatic” hydroxy groups but also encompasses polyhydric phenols, i.e. compounds having more than two “aromatic” hydroxy groups. Examples of useful dihydric phenols include resorcinol, catechol, hydroquinone, and polyphenols including p,p′-dihydroxydibenzyl, p,p′-dihydroxyphenylsulfone, p,p′-dihydroxybenzophenone, 2,2′-dihydroxyphenylsulfone, p,p′-dihydroxybenzophenone, 2,2-dihydroxy-1,1-dinaphrhylmethane, and the 2,2′, 2,3′, 2,4′, 3,3′, 3,4′, and 4,4′ isomers of dihydroxydiphenylmethane, dihydroxydiphenyldimethylmethane, dihydroxydiphenylethylmethylmethane, dihydroxy-diphenylmethylpropylmethane, dihydroxydiphenylethylphenylmethane, dihydroxydiphenyl-propylenphenylmethane, dihydroxydiphenylbutylphenylmethane, dihydroxydiphenyl-tolylethane, dihydroxydiphenyltolylmethylmethane, dihydroxydiphenyldicyclohexyl-methane, and dihydroxydiphenylcyclohexane.
Preferred epoxy resins include epoxy resins containing or consisting of glycidyl ethers or polyglycidyl ethers of dihydric or polyhydric phenols, such as for example, but not limited to bisphenol A, bisphenol F and combinations thereof. Instead of, or in addition to, using the aromatic epoxy resins described above also their fully or partially hydrogenated derivatives (i.e. the corresponding cycloaliphatic compounds) may be used.
Preferably the epoxy resin is liquid at room temperature but also solid epoxy resins, or resin particles may be used or may be used in dissolved form, for example in dissolved or dispersed in a solvent or another liquid resin.
Examples of commercially available epoxy resins include diglycidylether of bisphenol A (e.g. available under the trade designation EPON 828, EPON 830 or EPON 1001 from Hexion Speciality Chemicals GmbH, Rosbach, Germany, or under the trade designation D.E.R-331 or D.E.R-332 from Dow Chemical Co,); diglycidyl ether of bisphenol F (e.g. EPICLON 830 available from Dainippon Ink and Chemicals, Inc. or D.E.R.-354 from Dow Chemical Co, Schwalbach/Ts., Germany); silicone resins containing diglycidyl epoxy functionalities; flame retardant epoxy resins (e.g. DER 580, a brominated bisphenol type epoxy resin available from Dow Chemical Co.); Other epoxy resins based on bisphenols are commercially available under the trade designations EPIKOTE (Hexion Speciality Chemicals, Rosbach, Germany), D.E.N. (Dow Chemical Co, Schwalbach/Ts., Germany), or EPILOX (Leuna Epilox GmbH, Leuna, Germany).
Toughening agents are polymers, other than the epoxy resins, capable of increasing the toughness of cured epoxy resins compared to the same composition not containing them (the difference in amount in such comparison studies is made up by the epoxy resin) and otherwise treated identically. The toughness can be measured, for example, by the floating roller peel tests of the cured compositions as described in the example section provided herein.
The precursor compositions described herein contain two or more different core-shell polymers as toughening agents. It is believed that a combination of core-shell polymers increases the mechanical properties of the cured adhesives at low temperatures in particular at a temperature range of from about 0° C. to about −60° C. and more particular at −55° C., in particular their mechanical strength, as for example expressed a floating roller peel strength and/or overlap shear strength.
Core-shell polymers have a structure containing an internal part, referred to as core and an exterior part referred to as shell. Core and shell may be made of different polymers. The core of the core-shell polymer may comprise or consist of a polymer or copolymer of a diene, which means the polymer or copolymer comprises repeating units derived from an olefin having two unsaturations. Examples of such olefins include but are not limited to, butadiene and isobutadiene. The core of the core-shell polymer may also comprise a polymer or copolymer comprising repeating units derived from a lower alkyl acrylate (e.g. an alkyl acrylate containing up to 20 carbon atoms). Example of such alkyl acrylates include but are not limited to, n-butyl-, ethyl-, isobutyl- or 2-ethylhexylacrylate. The core of the core-shell polymers may also comprise silicone resins or copolymers thereof. The core of the core-shell polymers may also comprise copolymers of one or more of the afore-mentioned polymers styrene or a styrene-derivative. Examples of such copolymers include, but are not limited to butadiene-styrene copolymers.
The precursor formulations may contain, for example, a first core-shell polymer having a core comprising a silicone polymer or copolymer and a second core-shell polymer having a core comprising a diene polymer or copolymer, such as for example but not limited to a butadiene polymer or copolymer or a butadiene-styrene copolymer. The precursor formulations may also contain, for example, a first core-shell polymer having a core comprising a diene polymer and a second core-shell polymer also comprising a diene polymer but wherein the second core-shell polymer is chemically different than the first core-shell polymer, for example having a different diene polymer or a different comonomer or a different composition of the shell.
The core of the core-shell polymer is typically elastomeric. It typically has a low glass transition temperature (Tg) (e.g. a Tg of less than about −30° C., or preferably less than about −50° C.).
The shell of the core-shell polymer may contain the polymer of the core and one or more further copolymers. Typical copolymer include polymer containing repeating units derivable from unsaturated olefins (for example but not limited to monounsaturated olefins such as for example ethylenes, styrenes and the like), olefinic esters (for example but not limited to vinyl acetates), olefinic acids (for example but not limited to acrylates, methacrylates) or olefinic halogens (for example but not limited to vinyl chloride).
The shell may also not contain the polymer of the core but contains a polymer or copolymer comprising repeating units derivable from unsaturated olefins (for example but not limited to monounsaturated olefins such as for example ethylenes, styrenes and the like), olefinic esters (for example but not limited to vinyl acetates), olefinic acids (for example but not limited to acrylates, methacrylates) or olefinic halogens (for example but not limited to vinyl chloride). The core-shell polymer may or may not have reactive groups which can react with the epoxy resins or curing agents. The reactive groups may include, for example, epoxy groups, such as glycidyl ether groups, which may be introduced into the shell by using glycidyl methacrylate as monomer. In an embodiment of the invention, the core-shell polymer does not contain reactive groups that can react with the epoxy-resin or the curing agents comprised in the formulation, such as epoxy groups and/or amine groups.
Core-shell polymers can be prepared for example by polymerizing monomers until a certain particle size has been generated. The polymerization is then altered for example by changing the monomer feed such that a shell is polymerized around the particles. Alternatively, the shell can be grafted onto the core or introduced by cross-linking reactions. Examples of methods for making core-shell polymers can be found, for instance, in U.S. Pat. Nos. 5,186,993 to Hallden-Alberton and Wills and 4,315,085 to Ozari and Barabas, or European Patent application No 1,632,533 to Katsumi and Masakuni, which are all incorporated herein by reference.
The core-shell polymers may be solid. They may be particulate materials. The core-shell polymers may have an average particle size (number average) of from about 20 nm to about 4,000 nm or from about 50 nm to about 500 nm. The first and second core-shell polymer may have the same or different particle size ranges. The particle sizes may be determined by light diffraction or by electronic microscopy.
The core shell polymers may have several glass transition temperatures (core and shell material may be chemically different). The compositions provided herein preferably contain at least one core-shell polymer having at least one glass transition temperature (Tg) of less than about −30° C., or less than about −50° C. and even more preferably both the first and second core-shell polymer have at least one Tg of less than about −50° C. or even less than about −70° C.
In some embodiments the core-shell polymers at least one of the core-shell polymers contains repeating units derivable from butadiene, butadiene and styrene or butadiene, styrene and methacrylate. In some embodiments the precursor compositions contain one core-shell polymer comprising a silicone polymer or copolymer. In other embodiments the precursor compositions contain a core-shell polymer comprising repeating units derivable from butadiene and a core-shell polymer comprising a silicone polymer or copolymer.
Core shell polymers are commercially available, for example under the trade designation GENIOPERL (silicone-based core-shell polymers from Wacker Chemie, Munich, Germany), ALBIDUR (silicone-based core-shell polymers from Nanoresins, Geesthacht, Germany, PARALOID EXL (methacrylate-butadiene-styrene core-shell polymers from Rohm and Haas, Philadelphia, Pa., USA), or KANE ACE MX (from Kaneka, Brussels, Belgium). Most of the commercially available core-shell rubber products are dispersed in some quantity of epoxy resins, the epoxy equivalent weights are indicated by the suppliers. This introduced amount of epoxy resin has to be considered when making up the precursor composition and when adjusting the epoxy:hardener (curing agent) ratio.
In addition to the combination of core-shell polymers, the compositions may contain further toughening agents. Such toughening agents include liquid rubbers containing repeating units derived from butadiene or isobutadiene. The liquid rubber may be homo or copolymers, for example acrylate-copolymers. A particular example includes liquid butadiene acrylonitrile rubbers. Such liquid rubbers may or may not contain reactive end groups, such as for example amine-terminated rubber (ATBN) or carboxylate-terminated rubber (CTBN) or liquid rubbers containing free epoxy- or methacyrlate end-groups. Rubber means the polymers are elastomeric. The addition of a liquid butadiene rubber is believed to improve the mechanical strength of the cured adhesives at elevated temperatures, in particular at temperatures of 90° C., 120° C. or even 135° C. Liquid butadiene rubbers are commercially available, for example under the trade designation HYPRO from Nanoresins AG, Geesthacht, Germany.
Curing Agent System:
Curing agents suitable in the present invention are compounds which are capable of cross-linking (curing) the epoxy resin. Suitable curing agents according to the present invention are primary or secondary amines. The curing agent system comprises two amine curing agents, a first amine curing agent and a second amine curing agent being chemically different from the first one.
The first amine curing agent is an aliphatic, linear or branched, primary or secondary amine. The first amine curing agent may have the general structure:
wherein
the residues R1, R2, and R4, independently from each other, may represent hydrogen or a hydrocarbon (such as an alkyl) or an alkoxy or a polyoxyalkyl residue containing about 1 to 15 carbon atoms. R3 represents a hydrocarbon, an alkylether or a polyether alkyl residue, preferably containing about 1 to 15 carbon atoms. More preferably R3 is a polyetheralkyl residue. Preferably, the residues R1, R2, and R4 are chosen such that the amine contains at least one or two primary amine groups;
n represents 1, 2, 3, 4, 5, 6, 7, 8, 9 or an integer from 1 to 10.
Examples for suitable curing agents wherein R3 is an alkyl include ethylene diamine, diethylene diamine, triethylene tetraamine, propylene diamine, tetraethylene pentaamine, hexaethylene heptaamine, hexamethylene diamine, 2-methyl-1,5-pentamethylene-diamine, and the like.
Preferably, the first curing agent is a polyether amine having one or tow or more primary amine moieties. The polyether amine may have 1, 2, 3, 4, 5 or 6 or from 1 to 12, or from 1 to 6 catenary ether (oxygen) atoms. Suitable polyether amines include those that can be derived from polypropylene oxide or polyethylene oxide. Suitable polyether amines are commercially available under the trade designation JEFFAMINE from Huntsman Chemicals, or TTD (4,7,10-trioxatridecane-1,13-diamine) commercially available, for example, from BASF, Ludwigshafen Germany.
The second curing agent is a cycloaliphatic amine. The cycloaliphatic amines as used herein mean that the amine contains one or more than one cycloaliphatic residues. The cycloaliphatic amines are preferably primary amines and contain at least one primary amine group More preferably the cycloaliphatic residues contains one or more primary amine groups (e.g. —NH2 group). Typical examples of cycloaliphatic amines include primary amines containing one or two cyclohexyl, cycloheptyl, or cyclopentyl residues or combinations thereof. The cycloaliphatic residue is typically in α-, or β-position to the amine groups (α-position means directly bonded to the amine. (β-position means the position adjacent to the α-position). Particular examples of a cycloaliphatic amine curing agents include methylene dicyclohexylamines, methyl or dimethyl methylene dicyclohexylamines, isophorone amines or diamines. Suitable cycloaliphatic amine curing agents are commercially available under the trade designation ANCAMINE 2264, ANCAMINE 2280, ANCAMINE 2286 from Airproduct and Chemical Inc, Allentown, Pa., USA or BAXXODUR EC331 from BASF, Ludwigshafen, Germany.
The combination of first and second amine curing agents as described above is believed to improve the mechanical strength, as for example expressed as floating roller peel strength and/or overlap shear strength, of the cured adhesive compositions at temperature ranges from about 0° C. to about −55° C., or in particular at −55° C. The presence of the cycloaliphatic amine increase the mechanical strength of the cured compositions at elevated temperatures, such as for example at 120° C. or even 135° C. The first and second amine curing agents described above may typically be used in a amount of from about 3:2 to about 2:3 by equivalent weight (i.e. by their amine content).
Filler include, but are not limited to, talc, coal tar, carbon black, textile fibers, glass fibers, aramid pulp, boron fibers, carbon fibers, sheet silicates or clays (such as, for example, mica, bentonite, wollastonite, kaolin), phosphates, silica, inorganic or organic microspheres or beads or combination thereof. The mechanical strength of the cured compositions can be improved at room temperature, if the filler is a particle and not a fiber. In particular the filler particle is selected from amorphous silica, metal particles or powders, aluminium hydrates or glass spheres. The particles may be preferably spherical or substantially spherical particles. The filler particles may have a particle size of from about 0.5 to about 500 μm, or from about 1 to about 50 μm. Preferably, the majority of the filler particles has an average particle size of from about 0.8 to about 100 μm or from about 5 to about 50 μm. Filler particles include silica particles, in particular amorphous (non-hollow) silica particles, hollow silica particles (hollow glass microspheres), metal particles or aluminium hydrate particles. It has been found that the silica particles as described above may further improve the mechanical strength of the cured composition at elevated temperatures, in particular at a temperature of 135° C. Preferred filler particles include fused silica. In some embodiments the compositions contain amorphous silica particles such as, for example, fused silica and hollow glass microspheres. The presence of amorphous silica particles is believed to improve the mechanical strength of the cured adhesive composition at elevated temperatures, for example at a temperature range from about 120° to about 135° C.
Fused silica is available, for example, under the trade designation MINSIL from Minco Inc., Midway, USA. Hollow glass microspheres are available under the trade designation MICROBUBBLES from 3M Company, St. Paul, Minn., USA.
The precursor compositions contain the above-mentioned ingredients in such amounts that upon curing the desired mechanical strength will be achieved. By using the above-mentioned ingredients cured adhesives having one or more or all of the following properties can be prepared:
a) cured adhesives having a floating roller peel strength on aluminum substrates of at least 80 N/25 mm at −55° C. when using a 150 μm thick bond line (as measured according to DIN EN 2243-2 (2005);
b) cured adhesives having a floating roller peel strength on aluminum substrates of at least 135 N/25 mm at 23° C. when using a 150 μm thick bond line (as measured according to DIN EN 2243-2 (2005);
c) cured adhesives having a floating roller peel strength on aluminum substrates of at least 50 N/25 mm at 90° C. when using a 150 μm thick bond line (as measured according to DIN EN 2243-2 (2005);
d) cured adhesives having a floating roller peel strength on aluminum substrates of at least 20 N/25 mm at 135° C. when using a 150 μm thick bond line (as measured according to DIN EN 2243-2 (2005);
e) cured adhesives having properties a) and b) or a), b) and c);
f) cured adhesives having a floating roller peel strength on aluminum substrates of at least 80 N/25 mm at −55° C., 23° C. and 90° C.;
g) cured adhesives having a floating roller peel strength on aluminum substrates of at least 80 N/25 mm at −55° C., 23° C., 90° C. and of at least 20 N/25 mm, preferably at least 60N/25 mm at 135° C. when using a 150 μm thick bond line (as measured according to DIN EN 2243-2 (2005).
The adhesives can be cured by exposure to 80° C. for two hours.
Typically, the adhesive compositions are prepared from precursor composition containing in the part (B) from 40 to 80% wt of epoxy resins, from 10 to 40% wt. core-shell agents, from 5 to 30% fillers wherein the total amount of ingredients in part (B) gives 100%.
Typically, the part (A) of the precursor contains from 60 to 95% curing agents, and from 2 to 10% filler with the total amounts of ingredients being 100%.
The amount of amine curing agents is typically chosen as described above.
The compositions may further contain liquid polymer comprising repeating units derived from butadiene (liquid butadiene rubbers) in amounts of 5 to 40% wt in either part (B) or part (A) or in both. If the liquid butadiene rubber is reactive, meaning it has end groups that can participate in the curing reaction, such as for example amine-terminated butadiene rubbers they are preferably present in the (A) part of the composition together with the curing agents.
The compositions my further contain other ingredients in minor amounts, typically up to 20% wt or up to 10% wt in part (A) or up to 15 or up to 10% wt in part (B) of ingredients other than the types of ingredients described above.
For preparing the curable adhesive compositions parts (A) and (B) are combined. The ratio of part (A) to part (B) to be used for making the adhesive is preferably determined by their equivalent weights based on epoxy-group content and amine content respectively. Parts (A) and (B) are mixed in an equivalent weight ratio (of amine content to epoxy content) of about 1:1, preferably with a (small) excess of part (A).
The compositions may further contain other ingredients, to optimize the composition or to adapt them to specific applications. The optimum amounts of these ingredients can be identified by routine experimentation.
The compositions may further comprise adjuvants such reactive diluents, pigments, flame retardants, antioxidants, adhesion promoters, thixotropic agents, filler materials other than the filler particles mentioned above, secondary curatives, catalysts and the like.
Reactive diluents and thixotropic agents may be added to control the flow characteristics of the adhesive composition.
Thixotropic agents are added to the compositions to prevent the composition from having a water-like consistency or viscosity. Thixotropic agents typically are particulate materials having particle sizes of less than 50 nm. Preferred thixotropic agents include fumed silica. Thixotropic agents are commercially available under the trade designation Cab-O—Sil from Cabot, Schwalbach im Taunus, Germany, or Aerosil from Degussa Evonik GmbH, Frankfurt, Germany. Thixotropic agents may be present in part (A), part (B) or both. Typically, they may be present in an amount of up to 5% wt or up to 10% wt in part (A), (B) or in both.
Reactive diluents are monomeric epoxy-containing molecules. Preferably, they have a saturated or unsaturated cyclic backbone. Preferred reactive terminal ether portions include glycidyl ether. Examples of suitable diluents include the diglycidyl ether of resorcinol, diglycidyl ether of cyclohexane dimethanol, diglycidyl ether of neopentyl glycol, triglycidyl ether of trimethylolpropane. Commercially available reactive diluents are for example “Reactive Diluent 107” from Hexion or “Epodil 757” from Air Products and Chemical Inc, Allentown, Pa., USA.
Pigments may include inorganic or organic pigments including ferric oxide, brick dust, carbon black, titanium oxide and the like.
Secondary curatives include imidazoles, imidazole-salts, imidazolines or aromatic tertiary amines including those having the structure of formula:
wherein
R1 is H or alkyl, such as, e.g., methyl or ethyl, preferably methyl;
R3 and R4 may be, independently from each other, present or absent and when present
R5 and R6 are, independent from each other, alkyl, preferably CH3 or CH2CH3;
An example for a secondary curative is tris-2,4,6-(dimethylaminomethyl)phenol commercially available under the trade designation ANCAMINE K54 from Air Products and Chemicals Inc.
The composition may optionally contain metal salt catalysts for accelerating the curing reaction. Suitable catalysts which are operable in the present compositions include the group I metal, group II metal or lanthanoid salts wherein the anion is selected from nitrates, iodides, thiocyanates, triflates, alkoxides, perchlorates and sulfonates with the nitrates, iodides, thiocyanates, triflates and sulfonates including their hydrates being preferred. The preferred group I metal (cation) is lithium and the preferred group II metals are calcium and magnesium with calcium being especially preferred. Accordingly, preferred catalyst salts are lanthane nitrate, lanthane triflate, lithium iodide, lithium nitrate, calcium nitrate and their corresponding hydrates. In general, a catalytic amount of salt is employed. For most applications, the catalyst will be used from about 0.05 to less than 3.0 parts by weight based on the total weight of the total composition. Typically, a weight ratio of metal salt catalyst to secondary curing agent of from about 1:1 to about 3:1 may be employed.
The adhesive composition can be applied to the desired substrate by any convenient technique. It can be applied cold or be applied warm if desired. It can be applied by extruding it or it can be applied using mechanical application methods such as a caulking gun, or by pasting it onto the substrate. Generally, the adhesive is applied to one or both substrates. The substrates are contacted such that the adhesive is located between the substrates to be bonded together. After application, the structural adhesive is cured by heating the composition to a temperature at which the curing agent initiates cure of the epoxy resin composition. Generally, this temperature may be about 60° C. or about 80° C.
The adhesive of the invention can be used to bond a variety of substrates together including wood, metal, coated metal, aluminum, a variety of plastic and filled plastic substrates, fiberglass and the like. In one preferred embodiment, the adhesive is used to bond parts of an aircraft together or parts to aircrafts, i.e. the composition are used as a repair material for aircrafts. Such parts can be steel, coated steel, galvanized steel (such as electrogalvanized, hot-dip zinc coated steel or zinc/iron (galvaneal)-coated steel), aluminum, coated aluminum, plastic and filled plastic substrates.
An especially preferred structural adhesive of the invention also exhibits (when cured) mainly cohesive failure when evaluated in peel testing method as described below. It is generally desirable to have structural adhesives fail in a cohesive mode wherein the adhesive splits and portions of the adhesive remain adhered to each of the bonded surfaces. A bond that fails cohesively is referred to as being “robust”. A failure mode wherein an adhesive splits and portions of the adhesive do not remain adhered to each of the surface of the substrate are referred to as “adhesive failure mode”.
The following examples are provided to illustrate the invention but are not intended to limit the scope thereof. All parts and percentages are by weight unless otherwise indicated.
EPIKOTE 828 (Hexion Speciality Chemicals GmbH, Rosbach, Germany): epoxy resin based on diglycidylether of bisphenol-A).
PARALOID EXL 2600 (Rohm and Haas Company, Philadelphia, Pa./USA): methacrylate/butadiene/styrene polymer with core/shell architecture (white powder not dispersed in epoxy resin).
TTD (BASF, Ludwigshafen, Germany): 4,7,10-Trioxa-1,13-tridecane-diamine.
KANE ACE MX-156 (Kaneka, Belgium): butadiene-based core/shell polymer (25% wt) dispersed in epoxy resin (diglycidylether of bisphenol A).
KANE ACE MX-257 (Kaneka, Belgium): butadiene based core/shell polymer (37% wt) dispersed in epoxy resin (diglycidylether of bisphenol A).
CAB-O-SIL TS 720 (Cabot GmbH, Hanau, Germany), hydrophobic fumed silica—treated with polydimethyl-siloxane polymer.
AEROSIL 200 (Evonik Industries, Frankfurt, Germany), hydrophilic fumed silica.
AEROSIL 202 (Evonik Industries, Frankfurt, Germany), hydrophobic fumed silica.
ALBIDUR EP 2240 A (Nanoresins, Geesthacht, Germany), silicone based core-shell toughening agent (40% wt dispersed in epoxy resin).
ANCAMINE 2264 (Airproducts and Chemicals, Allentown, Pa., USA), cycloaliphatic amine curing agent.
ANCAMINE K54 (Airproducts and Chemicals, Allentown, Pa., USA), tertiary amine.
APYRAL 24 (Nabaltec GmbH Schwandorf, Germany), aluminum trihydrate.
BAXXODUR EC 331 (BASF, Ludwigshafen, Germany), cycloaliphatic amine curing agent.
FILLEX 7-AE1, (Osthoff-Petrasch, Norderstedt, Germany), modified wollastonite, filler.
GENIOPERLS P52 (Wacker Chemie, Munich, Germany), silicone based core-shell toughening agent.
HOP-Mix 2303-A0 (Osthoff-Petrasch, Norderstedt, Germany), glass fibers, filler.
HOP-Plastothix (Osthoff-Petrasch, Norderstedt, Germany), inorganic micro fibers, filler.
HYPRO 1300×21 ATBN (Nanoresins, Geesthacht, Germany), liquid nitrile butadiene rubber, toughening agent.
KAOLIN W ultrafine (Erbslöh, Krefeld, Germany) bentonite, filler.
MINSIL SF 20 (Minco Inc, Midway, USA) fused silica
NANOMER I.E30 (Nanocor, Hoffmann Estates, USA), modified bentonite, filler.
SILANE Z6040 (Dow Corning, Seneffe, Belgium), adhesion promoter.
Particle sizes may be determined by light diffraction or by electron microscopy.
Overlap shear strength was determined according to DIN EN 2243-1 (2005) using a tensile tester at a crosshead speed of 10 mm/min. The test-results were reported in MPa. The cohesive strength was measured on aluminium 2024 T3 clad, etched by chromic-sulfuric acid (etching for 15 min. at 70° C., bath composition: 27.5 w/w H2SO4 (density 1,82), 7.5 w/w Na2Cr2O7.2H2O, 65.0 w/w desalinated H2O, additives: 0.5 g/l aluminum, 1.5 g/l CuSO4.5H2O.)
Equipment: Zwick/Roell Z050 tensile-tester with thermal chamber (Zwick GmbH & Co. KG, Ulm, Germany)
Substrate: 100×25×1.6 mm strips of Aluminium 2024 T3 clad (available from Rocholl GmbH, Aglasterhausen, Germany), etched by chromic-sulfuric acid as described above.
Preparation of Test Assembly: the Adhesive is Applied on One End of a Test Strip Using a spatula followed by overlapping the ends of the treated strip with the end of the non-treated strip. The two ends were pressed against each other forming an overlap of 10 mm. Excess adhesive was then removed using a spatula. The overlapped strips were clamped at the adhesive ends using capacity binder clips. The clamped assembly was cured for 2 h at 80° C. in an air circulated oven at ambient humidity prior to being submitted to the overlap shear test according to DIN EN 2243-1.
Adhesive strength was measured on aluminium 2024 T3 clad, etched by chromic-sulfuric acid. The floating roller peel strength was determined according to DIN 2243-2 (2005) using a Zwick/Roell Z050 tensile-tester with thermal chamber (Zwick GmbH & Co. KG, Ulm, Germany) operating at a crosshead speed of 140 mm/min. The test results are reported in N/25 mm.
250×25×1.6 mm and 300×25×0.5 mm aluminium 2024 T3 clad (available from Rocholl GmbH, Aglasterhausen, Germany) were cleaned by immersion in methyl-ethylketone followed by FPL etching as described above. The strips were masked with a Teflon tape (PTFE Tape 3M 5490) leaving a blank area of 200 mm×25 mm in order avoid flow of the adhesive over the extended area during assembly of the strips. This guarantees a defined bondline resulting in a well defined crack during the measurement. The test adhesive is applied on the blank area of the 1.6 mm strip and on the blank area of the corresponding 0.5 m mm strip using a spatula. The strips were pressed against each other and residual adhesive was removed with a spatula. The assembly was clamped on both sides using capacity binder clips over the length of the bondline.
The amine curatives were heated to 80° C. Ancamine K54 was added and the mixture was stirred for further 5 minutes. The remaining ingredients were added at room temperature (23° C.) while stirring for 1 minute using a high speed mixer (DAC 150 FVZ Speedmixer, Hauschild Engineering, Germany) at 3000 rpm. The ingredients were added in small amounts to make sure the temperature does not increase over 100° C.
Epoxy resin and the predispersed core shell particles were mixed at 23° C. with stirring. If used, non-predispersed core-shell polymer (Paraloid EXL 2600) was added in small portions with stirring for 15 minutes. After an additional stirring for 30 minutes, the mixture was heated to 80° C. and held for 90 minutes. The solution was cooled down to room temperature. The remaining ingredients were subsequently added and homogenized with a high speed mixer (a DAC 150 FVZ Speedmixer, Hauschild Engineering, stirring at 3000 rpm for 1 minute after each addition at 23° C.).
Part A and Part B were mixed in a high speed mixer at 3000 rpm for 30 seconds. The compositions were then cured at 80° C. for 2 hours in an air-circulated oven at ambient humidity.
The floating roller peel strength of compositions containing various toughening agents was measured at 55° C. The cured compositions were obtained by combining the A part of table 1 with the different B parts of table 2 (B1-B5). B1 is a composition containing a core-shell toughening agent based on methacrylate-butadiene-styrene polymers. B2 is a composition comprising a silicone-based core-shell toughener. B3 contains a combination of the tougheners used in B1 and B2. B4 comprises a combination of a core-shell toughener with a toughening agent based on a liquid butadiene-nitrile rubber. B5 is a precursor composition comprising a combination of two core-shell polymers. Final adhesive were prepared by combining the B parts with the A parts. A and B parts were combined such that the equivalent weight ratio of A:B was 1.03:1.0.
The results of floating roller peel tests obtained with the cured samples indicate an improved mechanical strength for combinations of core-shell polymers (Ex 3, Ex 5) compared to the use of single core-shell polymers (Ex 1, Ex 2) or of a combination of a single core-shell polymer with another toughening agent (liquid butadiene rubber, Ex 4) at −55° C.
The floating roller peel strength at room temperature of compositions containing a combination of core shell toughening agents with different filler materials was examined. Adhesives were prepared by combining the A-part with the B-part as described above. All adhesive compositions tested were made up of the A-part composed as shown in table 4. The composition of the B-parts is shown in table 5. The results of the floating roller peel tests are shown in table 6.
The results represented in table 6 indicate that the mechanical strength at room temperature of an adhesive composition containing a combination of core-shell polymers can be increased when using filler particles rather than fibers or sheet-like materials such as clays or sheet silicates.
Compositions of example 8 (Ex 8, fused silica filler) and example 11 (Ex 11, aluminium hydrate filler) were measured for their overlap shear strength at high temperature (135° C.). The results shown in table 7 and 8 indicate that both filler materials are comparable at room and elevated temperature but that better mechanical strength at high temperatures (135°) can be obtained with a silica filler than with an aluminium hydrate filler.
The adhesive obtained by combining the precursor composition B7 of table 5 and the A part of table 4 was cured 2 hours at 80° C. The floating roller peel strength of the samples was measured at −55° C., 23° C., 90° C. and 135° C. and show very good mechanical strength over the temperature range from −55° C. up to 90° C. and satisfying mechanical strength even at 135° C.
The adhesive obtained by combining the precursor composition B7 of table 5 and various parts A as shown in table 10 were cured 2 hours at 80° C. The floating roller peel strength of the samples was measured at −55° C., 23° C. and 90° C. The results shown in table 11 show that a combination of curing agents improves the mechanical strength compared to the use of a single curing agent.
The following experiments shows that the mechanical strength of at very high temperatures (135° C.) of the above compositions can be further improved by adding a liquid butadiene rubber to the composition.
Parts A and B were combined (3.97 g of part A and 10.0 g of part B) and cured at 80° C. for 2 hours as described above. Floating roller T-peel tests and overlap shear tests were carried out on aluminum substrates at a 150 μm bond line as described above. The results are shown in table 14 below.
| Number | Date | Country | Kind |
|---|---|---|---|
| 091535922 | Feb 2009 | EP | regional |
| Filing Document | Filing Date | Country | Kind | 371c Date |
|---|---|---|---|---|
| PCT/US10/25345 | 2/25/2010 | WO | 00 | 9/9/2011 |
