CA2198755A1 - Radiation curable resins comprising hyperbranched polyesters - Google Patents
Radiation curable resins comprising hyperbranched polyestersInfo
- Publication number
- CA2198755A1 CA2198755A1 CA 2198755 CA2198755A CA2198755A1 CA 2198755 A1 CA2198755 A1 CA 2198755A1 CA 2198755 CA2198755 CA 2198755 CA 2198755 A CA2198755 A CA 2198755A CA 2198755 A1 CA2198755 A1 CA 2198755A1
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- Canada
- Prior art keywords
- anhydride
- meth
- hydroxyl groups
- acrylate
- hyperbranched polyester
- 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.)
- Abandoned
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-
- 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
- C08G83/00—Macromolecular compounds not provided for in groups C08G2/00 - C08G81/00
- C08G83/002—Dendritic macromolecules
- C08G83/005—Hyperbranched macromolecules
-
- 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
- C08G63/00—Macromolecular compounds obtained by reactions forming a carboxylic ester link in the main chain of the macromolecule
- C08G63/02—Polyesters derived from hydroxycarboxylic acids or from polycarboxylic acids and polyhydroxy compounds
- C08G63/12—Polyesters derived from hydroxycarboxylic acids or from polycarboxylic acids and polyhydroxy compounds derived from polycarboxylic acids and polyhydroxy compounds
- C08G63/123—Polyesters derived from hydroxycarboxylic acids or from polycarboxylic acids and polyhydroxy compounds derived from polycarboxylic acids and polyhydroxy compounds the acids or hydroxy compounds containing carbocyclic rings
- C08G63/127—Acids containing aromatic rings
-
- 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
- C08G63/00—Macromolecular compounds obtained by reactions forming a carboxylic ester link in the main chain of the macromolecule
- C08G63/02—Polyesters derived from hydroxycarboxylic acids or from polycarboxylic acids and polyhydroxy compounds
- C08G63/12—Polyesters derived from hydroxycarboxylic acids or from polycarboxylic acids and polyhydroxy compounds derived from polycarboxylic acids and polyhydroxy compounds
- C08G63/16—Dicarboxylic acids and dihydroxy compounds
- C08G63/20—Polyesters having been prepared in the presence of compounds having one reactive group or more than two reactive groups
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G63/00—Macromolecular compounds obtained by reactions forming a carboxylic ester link in the main chain of the macromolecule
- C08G63/02—Polyesters derived from hydroxycarboxylic acids or from polycarboxylic acids and polyhydroxy compounds
- C08G63/12—Polyesters derived from hydroxycarboxylic acids or from polycarboxylic acids and polyhydroxy compounds derived from polycarboxylic acids and polyhydroxy compounds
- C08G63/16—Dicarboxylic acids and dihydroxy compounds
- C08G63/20—Polyesters having been prepared in the presence of compounds having one reactive group or more than two reactive groups
- C08G63/21—Polyesters having been prepared in the presence of compounds having one reactive group or more than two reactive groups in the presence of unsaturated monocarboxylic acids or unsaturated monohydric alcohols or reactive derivatives thereof
-
- 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
- C08G63/00—Macromolecular compounds obtained by reactions forming a carboxylic ester link in the main chain of the macromolecule
- C08G63/02—Polyesters derived from hydroxycarboxylic acids or from polycarboxylic acids and polyhydroxy compounds
- C08G63/12—Polyesters derived from hydroxycarboxylic acids or from polycarboxylic acids and polyhydroxy compounds derived from polycarboxylic acids and polyhydroxy compounds
- C08G63/52—Polycarboxylic acids or polyhydroxy compounds in which at least one of the two components contains aliphatic unsaturation
- C08G63/56—Polyesters derived from ester-forming derivatives of polycarboxylic acids or of polyhydroxy compounds other than from esters thereof
- C08G63/58—Cyclic ethers; Cyclic carbonates; Cyclic sulfites ; Cyclic orthoesters
-
- 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]
- Y10T428/31786—Of polyester [e.g., alkyd, etc.]
-
- 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]
- Y10T428/31786—Of polyester [e.g., alkyd, etc.]
- Y10T428/31794—Of cross-linked polyester
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Macromonomer-Based Addition Polymer (AREA)
- Polyesters Or Polycarbonates (AREA)
- Polymerisation Methods In General (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
Abstract
Hyperbranched polyester of a polyol with 3 to 10 reactive hydroxyl groups, preferably of equivalent reactivity, and an aromatic polycarboxylic anhydride with 2 to 4 carboxyl groups, preferably 3 carboxyl groups, each hydroxyl group of the polyol forming an ester linkage with one anhydride group of the polycarboxylic anhydride, and further glycidyl (meth)acrylate or allyl glycidyl ether forming ester linkages with the remaining carboxyl groups of the anhydride and free hydroxyl groups. Further in the hyperbranched polyester (meth)acrylic anhydride and/or an aliphatic carboxylic anhydride form ester linkages with the free hydroxyl groups. The invention also comprises a process for the production of hyperbranched polyesters and such polyesters obtainable by the process. The hyperbranched polyesters can be used as resins, curable by UV irradiation, for the production of coatings, adhesives, laminates, foils and thin films and fibre-reinforced composites.
Description
~ W096/07688 ~ ~ ~ 9 8 7 g 5 PCTISE9~1013 ~ 1 Radiation curable resins comprising hyperbranched polyesters The present invention relates to new hyperbranched polyesters and a process for the production thereof and curable resins comprising the polyesters.
Radiation-curable resins are increasingly used in various industrial applications, replacing conventional thermally cured and solvent based coatings and adhesives. The radiation-curable resins have favourable properties, e.g., high speed and low energy consumption of cure, solvent-free formulations, room temperature operation and high quality end-products. The principal components of a radiation-curable resin are oligomers (or prepolymers) and comonomers. The oligomers constitute the backbone of the three-dimensional polymer network formed by curing. Important types of oligo-mers commonly used for coating are acrylated epoxies, acryla-ted polyurethanes, unsaturated polyesters and acrylated polyesters (or polyethers) which give desired properties of the final cured films. However, those oligomers usually consist of linear molecular ch~; n.q . The viscosity of the resin increases rapidly with increasing chain length of the oligomer. To obtain an operational viscosity of the formula for spraying, dipping, roll coating, etc., large amounts of multifunctional comonomer are required for the primary func-tion of viscosity control. In addition, the comonomers have important effects on the cure reaction and the properties of the final product. Some of the comonomers have low cure rate, cause shrinkage of the film during curing, and have high costs and a limited shelf life. Multifunctional acrylates are the preferred monomers in radiation-curable systems because of their rapid curing rates and low prices. The common acrylate monomers are volatile and toxic, and have strong odour. Therefore, the trend is to use radiation-curable oligomers with viscosity close to the required application viscosity in order to reduce or eliminate the use of comono-mers.
An object of the present invention therefore was toobtain oligomers with reduced viscosity compared to known CONFlR~ TlON
COPY
W096/076~ 2 ~ ~ 8 7 5 ~ P~ 0l3 oligomers with similar molecular weight.
A further object of the invention was to present oligomers which in resin applications needs a lower amount of multifunctional comonomers or none at all, while the resins still have a low viscosity, a high cure rate, an acceptable degree of curing and the final products have good mechanical properties.
A further object of the invention was to offer a process for the production of such oligomers.
The objects of the invention was solved by the hyperbranched polyester, the process for the production of these hyperbranched polyesters and resin comprising them, as claimed in the claims.
Oligomers with a strongly branched structure are a new family of polymers which has been attracting increasing interest for many applications, e.g., in agriculture, medi-cine, cosmetics, adhesives and coatings. The oligomers are referred to as hyperbranched polyesters with a three-dimen-sional molecular architecture and possessing starburst topology (D.A. O'Sullivan, Chem. Eng. News, 20 (1993); D.A.
Tomalia, A.M. Naylor, and W.A. Goddard III, Angew.Chem. Int.
Ed.Engl., 29, 138 (1990). An important structural difference between linear oligomers and hyperbranched polyesters is that a linear oligomer of sufficient molecular weight contains an entanglement of flexible molecular ch~;n-q, while a hyperbran-ched polyester is a compact molecule with many branches which carry a high number of terminal functional groups on each molecule.
With the present invention it was found that hyper-branched polyesters with reactive acrylate double bonds atchain extremities canbe used to reduce viscosity, increase reaction rate, and improve adhesion to substrates due to their very special molecular structures. This new kind of molecules modifies the physical and chemical properties both of the resin system and of the final product after curing, thereby facilitating their use in coating and adhesive sys-tems. Further, with the present invention hyperbranched W096/07688 ~ 9 8 7 5 5 PCT/~E9S/01013 polyesters with high molecular weight can be obtained in a simple proceæs from readily available and inexpensive raw materials.
Hyperbranched polyester research is still fairly new, and to date no commercial products are available. The main difficulties in preparing three-dimensional and ordered hyperbranched polyesters are preserving the regularity and order in the structures, characterization of the products, and separating the products from the excess of reactants.
Little work has been performed to prepare adhesive and coat-ing systems with hyperbranched polyesters, especially for radia~ion curing applications. A series of work on allyl ether maleate hyperbranched polyesters for W curing coatings have been reported (M.Johansson, E. Malmstrom, and A.Hult, J.Polym.Sci., Part A: Polym.Chem., 31, 619 (1993); E.Malm-strom and A.Hult ~Hyperbranched polyesters and their Degree of Branching as Determined by l3C-NMR", Proceedings of Nordic Polymer Days 1994.).
With the present invention it has been possible to synthesize a series of new hyperbranched (meth)acrylated polyesters with different number of terminal double bonds per molecule. The rheological properties of the resins prepared from the polyesters and the mechanical properties of W cured films are improved in a pronounced manner compared with known polymers.
Thus, the present invention relates to a hyperbran-ched polyester of a polyol with 3 to 10 reactive hydroxyl groups, preferably of equivalent reactivity, and an aromatic polycarboxylic anhydride with 2 to 4 carboxyl groups, prefer-ably with 3 carboxyl groups, each hydroxyl group of the polyol forming an esterlinkage with one anhydride group of the polycarboxylic anhydride, and further glycidyl (meth)acrylate or allyl glyci-dyl ether forming ester linkages with the remaining carboxylgroups of the anhydride and free hydroxyl groups.
The invention further relates to a hyperbranched W096/07688 ~ ~ ~ 9 ~ 7 ~ 9 PCT/SEgS/01013 polyester as defined above in which (meth)acrylic anhydride and/or an aliphatic carboxylic anhydride form/s ester link-ages with the free hydroxyl groups.
The present invention further relates to a process for the production of a hyperbranched polyester, and hyper-branched polyester obtainable by the process characterized in that it comprises the following steps:
a) reacting an aromatic polycarboxylic anhydride with 2 to 4 carboxyl groups, preferably 3 carboxyl groups, with a polyol with 3 to lO reactive hydroxyl groups, preferably of equival-ent reactivity, in the presence of an activating agent, the amount of anhydride being at least one mole of anhydride per hydroxyl group in the polyol, b) reacting the product from a) with glycidyl (meth)acrylate or allyl glycidyl ether in an amount at least corresponding to one mole of glycidyl (meth)acrylate or allyl glycidyl ether per free carboxylic acid group of the product of a).
The process and the polyester obtainable by the process can further comprise the following step:
c) the product from step b) is further reacted with (meth)-acrylic anhydride in an amount sufficient to esterify a part or all of the free hydroxyl groups of the product from step b). The products from step b) or c) can further be reacted with an aliphatic carboxylic anhydride in an amount to esterify a part of or all of the rem~;n;ng hydroxyl groups of the products.
Two principally different methods have been devel-oped for the synthesis of hyperbranched polymers: a conver-gent growth approach, where growth begins at the chain ends, and a divergent growth approach, where growth begins at a central core. In the present invention, the hyperbranched polyesters with terminal double bonds were synthesized by controlled stepwise divergent preparation, i.e., the syn-thesis started at the centre of the hyperbranched polyester.
Two or three steps were needed to obtain hyperbranched polyesters with a predetermined number of terminal double bonds located at the surface of the oligomeric sphere. The W096/~76~8 ~ 2 ~ 9 8 7 5 ~ PCT/SE95/01~13 reaction scheme for the synthesis of the hyperbranched polyester can be illustrated for a polyol with 4 hydroxyl groups as shown in Figure 1 (B is hydroxyl groups, and D is unsaturated groups). New nomenclature developed by K. L.
Wooley, J. M. J. Fréchet and C. J. Hawker, Polymer vol. 35, No. 21, 1994, names the starburst hyperbranched molecule of Figure 1 a dendritic polymer.
In the first reaction step an aromatic carboxylic anhydride with 2 to 4 carboxyl groups, preferably 3 carboxyl groups, and a polyol with 3 to 10 hydroxyl groups and an activating agent were heated to temperatures about or below 100C, preferably initially to 70 to 80C and gradually increasing to about 100C at the end of the reaction, in the presence of a solvent and under inert gas atmosphere, prefer-ably nitrogen atmosphere. The aromatic carboxylic anhydrideis most preferably 1,2,4-benzenetricarboxylic anhydride.
Suitable polyols are all polyols having 3 to 10 hydroxyl groups and the hydroxyl groups are preferably of equivalent reactivity, which means that the esterification of each hydroxyl group will proceed equally easy to start the build-ing up of the regular molecule. Examples of such polyols are trimethylolpropane, pentaerythritol or a dimer thereof, mono-and disaccharides, with pentaerythritol as a preferred embod-iment. The amount of added anhydride is at least one mole of 25 anhydride per hydroxyl group of the polyol, but preferably the anhydride is added in an excess amount. An excess of 20 -50 mol ~ is suitable. An activating agent is used to activate the anhydride group. The activating agent is present in a catalytic amount. As activating agent stannous chloride is a preferred embodiment. A suitable solvent is for example N,M-dimethylformamide (DMF).
For a product mixture of 1~2~4-benzenetricarboxylic anhydride with pentaerythritol the IR spectrum with residual 1,2,4-benzenetricarboxylic anhydride is shown by curve 1 in 3 5 Figure 2 . Toluene was used to wash the reaction product to remove the excess of 1, 2, 4 -benzenetricarboxylic anhydride until no peaks at 1760 and 1850 cm~l for anhydride groups could be observed, shown as curve 2 in Figure 2. The wide absorption bands at the range of 2750 to 3400 cm~1 in the IR
spectrum indicate the terminal carboxyl groups on the benzene ring. For this product mixture each polyolester of the poly-carboxylic acid anhydride has two carboxyl end groups. Threeisomer products could be obtained in this system, and the molecular structures are shown in Figure 3. The product is largely a mixture of meta and para isomers of the ester according to the relative reactivity of the anhydride and the carboxyl groups at low reaction temperature. A small amount of ortho isomer is expected to be a hydrolysis and reesteri-fication product of para and meta polyolester formed. The reaction of carboxyl and hydroxyl groups is favoured at elevated temperatures.
The polyolester was further reacted with glycidyl (meth)acrylate or allyl glycidyl ether in an amount at least corresponding to one mole of glycidyl (meth)acrylate or allyl glycidyl ether per free carboxylic acid group of the formed polyester, preferably in an excess amount, i.e. about 5 wt~.
Glycidyl acrylate is the preferred reactant. The reaction is carried out in a solvent, such as a mixture of DMF and toluene in the presences of a basic catalyst and an inhibitor for radical polymerization until no carboxyl groups could be detected by end-group titration. As basic catalysts common bases can be used, but benzyl dimethyl amine is preferred.
Conventional inhibitors such as hydroquinone is used. The reaction temperature is below 100C, preferably about 70C.
The IR spectrum of the product is shown as curve 3 in Figure 2. The appearance of the wide absorption at around 3460 cm~
means the formation of hydroxyl groups on the molecular ch~; nR due to reaction of epoxy and carboxyl groups. Finally, residual solvent was removed by evacuation at low tempera-ture. The ~inal "starburst" hyperbranched polyester products with double bonds at the end groups are translucent viscous liquids with one hydroxyl group at each end group. The mol-ecular structure, when started with pentaerythritol, is ideally sphere-like, with about 8 end-double bonds. The W096/07688 ~ 7 5 5 PCT/SE9S/01013 principal formula is shown in Figure 4.
The hydroxyl groups of the hyperbranched polyester with terminal double bonds were reacted further by ester formation with (meth)acrylic anhydride in an amount suffi-cient to esterify a part of or all of the free hydroxyl , ~ groups in order to prepare the hyperbranched polyester mol-ecules with further end-double bonds. Of the two acrylic anhydrides, the methacrylic anhydride is preferred. The hyperbranched polyester started from pentaerythritol with about 16 end-double bonds with the idealized formula is shown in Figure 5. The IR spectrum of the hyperbranched polyester with about 16 double bonds is shown by curve 4 in Figure 2.
Almost no peak for hydroxyl group could be observed.
In a last step the product with end-double bonds is reacted with an aliphatic carboxylic anhydride, preferably acetic anhydride to esterify a part of or all of the remain-ing hydroxyl groups on the molecular ch~; nR for decreasing molecular polarity of the hyperbranched polyester, and im-proving its compatibility with multifunctional comonomers.
This esterification can also be made of the hydroxyl groups of the hyperbranched polyester before the previous reaction with (meth)acrylic anhydride, thus omitting the further introduction of (meth)acrylic double bonds. The final hyper-branched polyester products with terminal double bonds after modifying, prepared in the present invention are fairly transparent colourless viscous li~uids. As shown in Figure 4 and 5 the double bonds are in end groups, located at the surface of the oligomeric sphere, which is highly favourable for W cure.
The polydispersity measured by GPC analysis (Figure 6) varied from 1,4 to l,9 at different reactant ratios and reaction temperatures with molecular weights of m~; m~lm 2500 obtained, which corresponds to a modified polyester molecule with four main branches. The wide molecular weight distribu-35 tion is mainly attributed to incomplete reaction between 1, 2, 4-benzenetricarboxylic anhydride and pentaerythritol, hyperbranched polyester fragmentation during hyperbranched . ;
8 7 5 ~ 8 polyester growth, and to the small excess of glycidyl (meth)acrylate monomer which react further with by-products in the system, responsive to W irradiation.
The hyperbranched polyester according to the inven-tion can be used as curable resins. The resins are preferablycured by W or EB radiation and most preferably by W radi-ation. The resins have lower viscosity than known oligomer resins and can be used without a comonomer or with lower amounts of comonomer than for conventional oligomer resins.
The W curing of the resin according to the invention is very rapid, down to parts of a second at room temperatur oper-ation. This means a high speed of cure and low energi con-sumption. The obtained products have a high glass transition temperature, resulting in products of high hardness, for example coatings or laminates with high surface hardness.
The resins are solvent free and can be prepared from 100 ~ of the hyperbranched polyester according to the invention. The resins can however, also comprise multifunc-tional monomers. A suitable amount of comonomer is 5 - 20 wt ~ and the rest 80 - 95 wt ~ being the hyberbranched polyester. The resins preferably comprise a photofragmenting initiator. The amount of photofragmenting initiator used is in the range 1 - 5 wt ~ based on the resin. Conventional photofragmenting initiators can be used and a preferred initiator is benzoyl dimethylketol. As multifunctional mono-mers compounds with reactive double bonds can be used, such as trimethylolpropane tri(meth)acrylate, he~n~;ol diacryla-te, trimethylolpropane triallylether, pentaerythritol tri/te-tra-allylether, triallylcyanurate, trimethylolpropane tri-acrylether, pentaerythritol tetraacrylether. Trimethylolpro-pane triacrylate being a preferred embodiment.
The resin according to the invention can be used in many different fields of whick could be mentioned coatings, adhesives, laminates, foils and thin films and fibre-rein-forced composites.
The invention will now be illustrated withthe following examples which however, are not intended to W096/07688 PcTISE9S/01013 ~ 2 ~ ~ 8 7~ ~
restrict the invention. With parts and per cent are meant parts per weight and weight-~, if nothing else is mentioned.
The followinq chemicals are used:
Pentaerythritol [PETL]
1,2,4-Benzenetricarboxylic Anhydride [BTCA]
Glycidyl Acrylate [GA]
Methacrylic Anhydride [MAA]
Acetic Anhydride [AA]
Stannous Chloride [SC]
Benzyldimethylamine [BDMA]
Hydroquinone [HQ]
Dimethyl Formamide [DMF]
Trimethylolpropane Triacrylate (TMPTA) senzoyldimethylketol (BDK) Exam~le 1 92,2 g (0.48 mol) BTCA is dissolved in 100 ml DMF
at 80C. 10.9 g (0.08 mol) PETL and 0.1 g (0.1 wt~) SC are added, and the solution is kept at 80C for 8 hours, and then heated to 100C for 10 hours under N2. Most of DMF is distilled off in vacuum and toluene is poured into the prod-uct to dissolve the residual BTCA. The product is washed with toluene until no BTCA is detected in IR spectra (1760 and 1850 cm~l for anhydride groups). 57.2 g polyolester is obtained, as a white powder, with the yield of about 79 ~
after completely removing the solvents. The acid number of 475 mg KOH/g polyester is determined by titration with 0.1 N
KOH. 65.09 g (0.508 mol with a 5 ~ excess) GA is added slowly drop by drop at 70C together with 5 g (2.5 ~) BDMA as cata-lyst and 1000 ppm HQ as inhibitor, dissolved in 70 ml DMF.
After 7 hours at 70C no carboxyl groups can be detected by titration. DMF is distilled off in vacuum. The product is a viscous liquid with maximum 8 acrylate and 8 hydroxyl groups per molecule. This product is called D-lOH.
12.4 g (0.121 mol) AA is added to 40.8 g D-lOH in 50 ml DMF which reacts with about 6 hydroxyl groups per .
8 7 ~ 5 lo ~olecule (averaged about 2 OH groups per molecule remain).
The product solution is then heated for 2 hours at 70C and DMF i8 distilled off in vacuum. The obtained product, called D-1, is a viscous liquid with about 8 acrylate groups and 2 hydroxyl groups per molecule.
Exam~le 2 40.8 g D-lOH is dissolved in 50 ml DMF with 500 ppm HQ and 12.4 g (0.08 mol) MAA and 4.1 g (0.04 mol) AA are added slowly, drop by drop at 70C for two hours to react with the hydroxyl groups. DMF is removed by vacuum distilla-tion. The product, called D-2, is a viscous liquid with about 12 (meth)acrylate groups and 2 hydroxyl groups per molecule.
Exam~le 3 40.8 g D-lOH is dissolved in 50 ml DMF with 500 ppm HQ as inhibitor. 24.8 g MAA (0.161 mol) is added and heated to 70C. After 2 hours the reaction is complete. DMF is removed by vacuum distillation. The product, called D-3, is a viscous liquid with about 8 acrylate and 8 methacrylate groups per molecule.
The dynamic viscosity for the products from Examples 1 to 3 was measured as a function of frequency for the hyperbranched polyesters with different numbers of double bonds, as shown in Figure 7. The hyperbranched polyester D-1-OH, according to Example 1, with about 8 double bonds and without acetic anhydride modification, has the highest vis-cosity due to the many hydroxyl groups in the system, resul-ting in intermolecular hydrogen bonding (hyperbranched polyester aggregation). At decreasing hydroxy functionality, the dynamic viscosities of the hyperbranched polyester large-ly decrease in order of D-1, D-2 and D-3, according to Examples 1 to 3, at lower frequency. D-3 has the lowest viscosity compared with D-1 and D-2 because of the high number of double bonds (no remaining hydroxyl groups) at the surface of the spherical molecule. This results in increasing symmetry of the hyperbranched molecule, apart from less W096/07688 ~ 2 ~ 9 PCT/SE9S/01013 influence from the hydrogen bonding.
Low viscosity is particularly important in control-ling the levelling time of a coating and for evaluation of the processability of a radiation curable coating and adhes-ive. This is especially the case for lO0~ solid coatingsystems for thin films. The oligomer is the principal consti-tuent and primarily responsible for the basic properties of the coating. The viscosity of the oligomer is, therefore, an important parameter since it determines the amount of oligomer required in the final product. For control of the viscosity of the radiation curable resin there are only two parameters, namely the viscosity of the oligomer and the amount of comonomer added.
The principal rheological difference between the branched and the linear polyester molecules lies in the smaller spatial extension of the branched molecule at a glven molecular mass. The viscosity of the resin is related to the dynamic extension in space and the segment density within the volume of the molecule. Therefore, the sphere-like starburst (meth)acrylated polyester according to the invention has lower viscosity than the linear polyester.
Flow time measurements are another evaluation of the relative viscosity of various coatings and adhesives, using a viscosimetric cup. The viscosities of the hyperbran-ched (meth)acrylated polyesters containing 15 wt~ tri-methylolpropane triacrylate (TMPTA), as comonomer and a conventional epoxy acrylate modified unsaturated polyester (MUP) containing 35 wt~ TMPTA at 21C are compared in Figure 8. It can be seen that the flow times through the viscosimet-ric cup for hyperbranched polyester resins are much shorterthan for MUP resin. This means that the viscosity of MUP is much higher than that of hyperbranched polyester. A practical consequence is that the processability of hyperbranched polyester containing resins i8 improved due to lower viscos-ity.Exam~le 4:
Radiation-curable resins are increasingly used in various industrial applications, replacing conventional thermally cured and solvent based coatings and adhesives. The radiation-curable resins have favourable properties, e.g., high speed and low energy consumption of cure, solvent-free formulations, room temperature operation and high quality end-products. The principal components of a radiation-curable resin are oligomers (or prepolymers) and comonomers. The oligomers constitute the backbone of the three-dimensional polymer network formed by curing. Important types of oligo-mers commonly used for coating are acrylated epoxies, acryla-ted polyurethanes, unsaturated polyesters and acrylated polyesters (or polyethers) which give desired properties of the final cured films. However, those oligomers usually consist of linear molecular ch~; n.q . The viscosity of the resin increases rapidly with increasing chain length of the oligomer. To obtain an operational viscosity of the formula for spraying, dipping, roll coating, etc., large amounts of multifunctional comonomer are required for the primary func-tion of viscosity control. In addition, the comonomers have important effects on the cure reaction and the properties of the final product. Some of the comonomers have low cure rate, cause shrinkage of the film during curing, and have high costs and a limited shelf life. Multifunctional acrylates are the preferred monomers in radiation-curable systems because of their rapid curing rates and low prices. The common acrylate monomers are volatile and toxic, and have strong odour. Therefore, the trend is to use radiation-curable oligomers with viscosity close to the required application viscosity in order to reduce or eliminate the use of comono-mers.
An object of the present invention therefore was toobtain oligomers with reduced viscosity compared to known CONFlR~ TlON
COPY
W096/076~ 2 ~ ~ 8 7 5 ~ P~ 0l3 oligomers with similar molecular weight.
A further object of the invention was to present oligomers which in resin applications needs a lower amount of multifunctional comonomers or none at all, while the resins still have a low viscosity, a high cure rate, an acceptable degree of curing and the final products have good mechanical properties.
A further object of the invention was to offer a process for the production of such oligomers.
The objects of the invention was solved by the hyperbranched polyester, the process for the production of these hyperbranched polyesters and resin comprising them, as claimed in the claims.
Oligomers with a strongly branched structure are a new family of polymers which has been attracting increasing interest for many applications, e.g., in agriculture, medi-cine, cosmetics, adhesives and coatings. The oligomers are referred to as hyperbranched polyesters with a three-dimen-sional molecular architecture and possessing starburst topology (D.A. O'Sullivan, Chem. Eng. News, 20 (1993); D.A.
Tomalia, A.M. Naylor, and W.A. Goddard III, Angew.Chem. Int.
Ed.Engl., 29, 138 (1990). An important structural difference between linear oligomers and hyperbranched polyesters is that a linear oligomer of sufficient molecular weight contains an entanglement of flexible molecular ch~;n-q, while a hyperbran-ched polyester is a compact molecule with many branches which carry a high number of terminal functional groups on each molecule.
With the present invention it was found that hyper-branched polyesters with reactive acrylate double bonds atchain extremities canbe used to reduce viscosity, increase reaction rate, and improve adhesion to substrates due to their very special molecular structures. This new kind of molecules modifies the physical and chemical properties both of the resin system and of the final product after curing, thereby facilitating their use in coating and adhesive sys-tems. Further, with the present invention hyperbranched W096/07688 ~ 9 8 7 5 5 PCT/~E9S/01013 polyesters with high molecular weight can be obtained in a simple proceæs from readily available and inexpensive raw materials.
Hyperbranched polyester research is still fairly new, and to date no commercial products are available. The main difficulties in preparing three-dimensional and ordered hyperbranched polyesters are preserving the regularity and order in the structures, characterization of the products, and separating the products from the excess of reactants.
Little work has been performed to prepare adhesive and coat-ing systems with hyperbranched polyesters, especially for radia~ion curing applications. A series of work on allyl ether maleate hyperbranched polyesters for W curing coatings have been reported (M.Johansson, E. Malmstrom, and A.Hult, J.Polym.Sci., Part A: Polym.Chem., 31, 619 (1993); E.Malm-strom and A.Hult ~Hyperbranched polyesters and their Degree of Branching as Determined by l3C-NMR", Proceedings of Nordic Polymer Days 1994.).
With the present invention it has been possible to synthesize a series of new hyperbranched (meth)acrylated polyesters with different number of terminal double bonds per molecule. The rheological properties of the resins prepared from the polyesters and the mechanical properties of W cured films are improved in a pronounced manner compared with known polymers.
Thus, the present invention relates to a hyperbran-ched polyester of a polyol with 3 to 10 reactive hydroxyl groups, preferably of equivalent reactivity, and an aromatic polycarboxylic anhydride with 2 to 4 carboxyl groups, prefer-ably with 3 carboxyl groups, each hydroxyl group of the polyol forming an esterlinkage with one anhydride group of the polycarboxylic anhydride, and further glycidyl (meth)acrylate or allyl glyci-dyl ether forming ester linkages with the remaining carboxylgroups of the anhydride and free hydroxyl groups.
The invention further relates to a hyperbranched W096/07688 ~ ~ ~ 9 ~ 7 ~ 9 PCT/SEgS/01013 polyester as defined above in which (meth)acrylic anhydride and/or an aliphatic carboxylic anhydride form/s ester link-ages with the free hydroxyl groups.
The present invention further relates to a process for the production of a hyperbranched polyester, and hyper-branched polyester obtainable by the process characterized in that it comprises the following steps:
a) reacting an aromatic polycarboxylic anhydride with 2 to 4 carboxyl groups, preferably 3 carboxyl groups, with a polyol with 3 to lO reactive hydroxyl groups, preferably of equival-ent reactivity, in the presence of an activating agent, the amount of anhydride being at least one mole of anhydride per hydroxyl group in the polyol, b) reacting the product from a) with glycidyl (meth)acrylate or allyl glycidyl ether in an amount at least corresponding to one mole of glycidyl (meth)acrylate or allyl glycidyl ether per free carboxylic acid group of the product of a).
The process and the polyester obtainable by the process can further comprise the following step:
c) the product from step b) is further reacted with (meth)-acrylic anhydride in an amount sufficient to esterify a part or all of the free hydroxyl groups of the product from step b). The products from step b) or c) can further be reacted with an aliphatic carboxylic anhydride in an amount to esterify a part of or all of the rem~;n;ng hydroxyl groups of the products.
Two principally different methods have been devel-oped for the synthesis of hyperbranched polymers: a conver-gent growth approach, where growth begins at the chain ends, and a divergent growth approach, where growth begins at a central core. In the present invention, the hyperbranched polyesters with terminal double bonds were synthesized by controlled stepwise divergent preparation, i.e., the syn-thesis started at the centre of the hyperbranched polyester.
Two or three steps were needed to obtain hyperbranched polyesters with a predetermined number of terminal double bonds located at the surface of the oligomeric sphere. The W096/~76~8 ~ 2 ~ 9 8 7 5 ~ PCT/SE95/01~13 reaction scheme for the synthesis of the hyperbranched polyester can be illustrated for a polyol with 4 hydroxyl groups as shown in Figure 1 (B is hydroxyl groups, and D is unsaturated groups). New nomenclature developed by K. L.
Wooley, J. M. J. Fréchet and C. J. Hawker, Polymer vol. 35, No. 21, 1994, names the starburst hyperbranched molecule of Figure 1 a dendritic polymer.
In the first reaction step an aromatic carboxylic anhydride with 2 to 4 carboxyl groups, preferably 3 carboxyl groups, and a polyol with 3 to 10 hydroxyl groups and an activating agent were heated to temperatures about or below 100C, preferably initially to 70 to 80C and gradually increasing to about 100C at the end of the reaction, in the presence of a solvent and under inert gas atmosphere, prefer-ably nitrogen atmosphere. The aromatic carboxylic anhydrideis most preferably 1,2,4-benzenetricarboxylic anhydride.
Suitable polyols are all polyols having 3 to 10 hydroxyl groups and the hydroxyl groups are preferably of equivalent reactivity, which means that the esterification of each hydroxyl group will proceed equally easy to start the build-ing up of the regular molecule. Examples of such polyols are trimethylolpropane, pentaerythritol or a dimer thereof, mono-and disaccharides, with pentaerythritol as a preferred embod-iment. The amount of added anhydride is at least one mole of 25 anhydride per hydroxyl group of the polyol, but preferably the anhydride is added in an excess amount. An excess of 20 -50 mol ~ is suitable. An activating agent is used to activate the anhydride group. The activating agent is present in a catalytic amount. As activating agent stannous chloride is a preferred embodiment. A suitable solvent is for example N,M-dimethylformamide (DMF).
For a product mixture of 1~2~4-benzenetricarboxylic anhydride with pentaerythritol the IR spectrum with residual 1,2,4-benzenetricarboxylic anhydride is shown by curve 1 in 3 5 Figure 2 . Toluene was used to wash the reaction product to remove the excess of 1, 2, 4 -benzenetricarboxylic anhydride until no peaks at 1760 and 1850 cm~l for anhydride groups could be observed, shown as curve 2 in Figure 2. The wide absorption bands at the range of 2750 to 3400 cm~1 in the IR
spectrum indicate the terminal carboxyl groups on the benzene ring. For this product mixture each polyolester of the poly-carboxylic acid anhydride has two carboxyl end groups. Threeisomer products could be obtained in this system, and the molecular structures are shown in Figure 3. The product is largely a mixture of meta and para isomers of the ester according to the relative reactivity of the anhydride and the carboxyl groups at low reaction temperature. A small amount of ortho isomer is expected to be a hydrolysis and reesteri-fication product of para and meta polyolester formed. The reaction of carboxyl and hydroxyl groups is favoured at elevated temperatures.
The polyolester was further reacted with glycidyl (meth)acrylate or allyl glycidyl ether in an amount at least corresponding to one mole of glycidyl (meth)acrylate or allyl glycidyl ether per free carboxylic acid group of the formed polyester, preferably in an excess amount, i.e. about 5 wt~.
Glycidyl acrylate is the preferred reactant. The reaction is carried out in a solvent, such as a mixture of DMF and toluene in the presences of a basic catalyst and an inhibitor for radical polymerization until no carboxyl groups could be detected by end-group titration. As basic catalysts common bases can be used, but benzyl dimethyl amine is preferred.
Conventional inhibitors such as hydroquinone is used. The reaction temperature is below 100C, preferably about 70C.
The IR spectrum of the product is shown as curve 3 in Figure 2. The appearance of the wide absorption at around 3460 cm~
means the formation of hydroxyl groups on the molecular ch~; nR due to reaction of epoxy and carboxyl groups. Finally, residual solvent was removed by evacuation at low tempera-ture. The ~inal "starburst" hyperbranched polyester products with double bonds at the end groups are translucent viscous liquids with one hydroxyl group at each end group. The mol-ecular structure, when started with pentaerythritol, is ideally sphere-like, with about 8 end-double bonds. The W096/07688 ~ 7 5 5 PCT/SE9S/01013 principal formula is shown in Figure 4.
The hydroxyl groups of the hyperbranched polyester with terminal double bonds were reacted further by ester formation with (meth)acrylic anhydride in an amount suffi-cient to esterify a part of or all of the free hydroxyl , ~ groups in order to prepare the hyperbranched polyester mol-ecules with further end-double bonds. Of the two acrylic anhydrides, the methacrylic anhydride is preferred. The hyperbranched polyester started from pentaerythritol with about 16 end-double bonds with the idealized formula is shown in Figure 5. The IR spectrum of the hyperbranched polyester with about 16 double bonds is shown by curve 4 in Figure 2.
Almost no peak for hydroxyl group could be observed.
In a last step the product with end-double bonds is reacted with an aliphatic carboxylic anhydride, preferably acetic anhydride to esterify a part of or all of the remain-ing hydroxyl groups on the molecular ch~; nR for decreasing molecular polarity of the hyperbranched polyester, and im-proving its compatibility with multifunctional comonomers.
This esterification can also be made of the hydroxyl groups of the hyperbranched polyester before the previous reaction with (meth)acrylic anhydride, thus omitting the further introduction of (meth)acrylic double bonds. The final hyper-branched polyester products with terminal double bonds after modifying, prepared in the present invention are fairly transparent colourless viscous li~uids. As shown in Figure 4 and 5 the double bonds are in end groups, located at the surface of the oligomeric sphere, which is highly favourable for W cure.
The polydispersity measured by GPC analysis (Figure 6) varied from 1,4 to l,9 at different reactant ratios and reaction temperatures with molecular weights of m~; m~lm 2500 obtained, which corresponds to a modified polyester molecule with four main branches. The wide molecular weight distribu-35 tion is mainly attributed to incomplete reaction between 1, 2, 4-benzenetricarboxylic anhydride and pentaerythritol, hyperbranched polyester fragmentation during hyperbranched . ;
8 7 5 ~ 8 polyester growth, and to the small excess of glycidyl (meth)acrylate monomer which react further with by-products in the system, responsive to W irradiation.
The hyperbranched polyester according to the inven-tion can be used as curable resins. The resins are preferablycured by W or EB radiation and most preferably by W radi-ation. The resins have lower viscosity than known oligomer resins and can be used without a comonomer or with lower amounts of comonomer than for conventional oligomer resins.
The W curing of the resin according to the invention is very rapid, down to parts of a second at room temperatur oper-ation. This means a high speed of cure and low energi con-sumption. The obtained products have a high glass transition temperature, resulting in products of high hardness, for example coatings or laminates with high surface hardness.
The resins are solvent free and can be prepared from 100 ~ of the hyperbranched polyester according to the invention. The resins can however, also comprise multifunc-tional monomers. A suitable amount of comonomer is 5 - 20 wt ~ and the rest 80 - 95 wt ~ being the hyberbranched polyester. The resins preferably comprise a photofragmenting initiator. The amount of photofragmenting initiator used is in the range 1 - 5 wt ~ based on the resin. Conventional photofragmenting initiators can be used and a preferred initiator is benzoyl dimethylketol. As multifunctional mono-mers compounds with reactive double bonds can be used, such as trimethylolpropane tri(meth)acrylate, he~n~;ol diacryla-te, trimethylolpropane triallylether, pentaerythritol tri/te-tra-allylether, triallylcyanurate, trimethylolpropane tri-acrylether, pentaerythritol tetraacrylether. Trimethylolpro-pane triacrylate being a preferred embodiment.
The resin according to the invention can be used in many different fields of whick could be mentioned coatings, adhesives, laminates, foils and thin films and fibre-rein-forced composites.
The invention will now be illustrated withthe following examples which however, are not intended to W096/07688 PcTISE9S/01013 ~ 2 ~ ~ 8 7~ ~
restrict the invention. With parts and per cent are meant parts per weight and weight-~, if nothing else is mentioned.
The followinq chemicals are used:
Pentaerythritol [PETL]
1,2,4-Benzenetricarboxylic Anhydride [BTCA]
Glycidyl Acrylate [GA]
Methacrylic Anhydride [MAA]
Acetic Anhydride [AA]
Stannous Chloride [SC]
Benzyldimethylamine [BDMA]
Hydroquinone [HQ]
Dimethyl Formamide [DMF]
Trimethylolpropane Triacrylate (TMPTA) senzoyldimethylketol (BDK) Exam~le 1 92,2 g (0.48 mol) BTCA is dissolved in 100 ml DMF
at 80C. 10.9 g (0.08 mol) PETL and 0.1 g (0.1 wt~) SC are added, and the solution is kept at 80C for 8 hours, and then heated to 100C for 10 hours under N2. Most of DMF is distilled off in vacuum and toluene is poured into the prod-uct to dissolve the residual BTCA. The product is washed with toluene until no BTCA is detected in IR spectra (1760 and 1850 cm~l for anhydride groups). 57.2 g polyolester is obtained, as a white powder, with the yield of about 79 ~
after completely removing the solvents. The acid number of 475 mg KOH/g polyester is determined by titration with 0.1 N
KOH. 65.09 g (0.508 mol with a 5 ~ excess) GA is added slowly drop by drop at 70C together with 5 g (2.5 ~) BDMA as cata-lyst and 1000 ppm HQ as inhibitor, dissolved in 70 ml DMF.
After 7 hours at 70C no carboxyl groups can be detected by titration. DMF is distilled off in vacuum. The product is a viscous liquid with maximum 8 acrylate and 8 hydroxyl groups per molecule. This product is called D-lOH.
12.4 g (0.121 mol) AA is added to 40.8 g D-lOH in 50 ml DMF which reacts with about 6 hydroxyl groups per .
8 7 ~ 5 lo ~olecule (averaged about 2 OH groups per molecule remain).
The product solution is then heated for 2 hours at 70C and DMF i8 distilled off in vacuum. The obtained product, called D-1, is a viscous liquid with about 8 acrylate groups and 2 hydroxyl groups per molecule.
Exam~le 2 40.8 g D-lOH is dissolved in 50 ml DMF with 500 ppm HQ and 12.4 g (0.08 mol) MAA and 4.1 g (0.04 mol) AA are added slowly, drop by drop at 70C for two hours to react with the hydroxyl groups. DMF is removed by vacuum distilla-tion. The product, called D-2, is a viscous liquid with about 12 (meth)acrylate groups and 2 hydroxyl groups per molecule.
Exam~le 3 40.8 g D-lOH is dissolved in 50 ml DMF with 500 ppm HQ as inhibitor. 24.8 g MAA (0.161 mol) is added and heated to 70C. After 2 hours the reaction is complete. DMF is removed by vacuum distillation. The product, called D-3, is a viscous liquid with about 8 acrylate and 8 methacrylate groups per molecule.
The dynamic viscosity for the products from Examples 1 to 3 was measured as a function of frequency for the hyperbranched polyesters with different numbers of double bonds, as shown in Figure 7. The hyperbranched polyester D-1-OH, according to Example 1, with about 8 double bonds and without acetic anhydride modification, has the highest vis-cosity due to the many hydroxyl groups in the system, resul-ting in intermolecular hydrogen bonding (hyperbranched polyester aggregation). At decreasing hydroxy functionality, the dynamic viscosities of the hyperbranched polyester large-ly decrease in order of D-1, D-2 and D-3, according to Examples 1 to 3, at lower frequency. D-3 has the lowest viscosity compared with D-1 and D-2 because of the high number of double bonds (no remaining hydroxyl groups) at the surface of the spherical molecule. This results in increasing symmetry of the hyperbranched molecule, apart from less W096/07688 ~ 2 ~ 9 PCT/SE9S/01013 influence from the hydrogen bonding.
Low viscosity is particularly important in control-ling the levelling time of a coating and for evaluation of the processability of a radiation curable coating and adhes-ive. This is especially the case for lO0~ solid coatingsystems for thin films. The oligomer is the principal consti-tuent and primarily responsible for the basic properties of the coating. The viscosity of the oligomer is, therefore, an important parameter since it determines the amount of oligomer required in the final product. For control of the viscosity of the radiation curable resin there are only two parameters, namely the viscosity of the oligomer and the amount of comonomer added.
The principal rheological difference between the branched and the linear polyester molecules lies in the smaller spatial extension of the branched molecule at a glven molecular mass. The viscosity of the resin is related to the dynamic extension in space and the segment density within the volume of the molecule. Therefore, the sphere-like starburst (meth)acrylated polyester according to the invention has lower viscosity than the linear polyester.
Flow time measurements are another evaluation of the relative viscosity of various coatings and adhesives, using a viscosimetric cup. The viscosities of the hyperbran-ched (meth)acrylated polyesters containing 15 wt~ tri-methylolpropane triacrylate (TMPTA), as comonomer and a conventional epoxy acrylate modified unsaturated polyester (MUP) containing 35 wt~ TMPTA at 21C are compared in Figure 8. It can be seen that the flow times through the viscosimet-ric cup for hyperbranched polyester resins are much shorterthan for MUP resin. This means that the viscosity of MUP is much higher than that of hyperbranched polyester. A practical consequence is that the processability of hyperbranched polyester containing resins i8 improved due to lower viscos-ity.Exam~le 4:
3 parts of BDK were dissolved in 100 parts of a .
W096/07688 . PCT/SE95/01013 oa9 9~7~
mixture of 15 ~ by weight of TMPTA and 85 ~ by weight of D-1, D-2 or D-3, the resultant resins were coated on a polyethylene terephtalate (PET) sheet. The test samples were cured in air on a conveyer belt with variable speed by W
irradiation for 0,15 seconds under a 300 W/in (120 W/cm) Model F300 D bulb (Fusion W Curing Systems) in the exposure chamber.
Example 5:
The procedure of Example 4 was repeated except that 100 parts of D-1, D-2 or D-3 polyesters are used instead of the mixture of the polyesters and TMPTA.
The irradiation time is varied by changing the speed of the conveyor belt. The polymerization rate of the hyperbranched polyester resins was determined by measuring the irradiation time required to obtain fully tack-free state for the cured film using a cotton bar. The data are given in Figure 9. The resin with oligomer D-3 needs the shortest curing time to get tack-free state.
The glass transition temperatures of the crosslin-ked (meth)acrylated hyperbranched polyesters D-1, D-2 and D-3 according to Example 5 from Dynamic Mechanical Thermal Analy-sis (DMTA) measurements are given in Figure 10. It can be seen that the glass transition temperature increases rapidly with increasing functionality of the cured hyperbranched oligomer.
The physical properties of the cured material are related to the structure of the crosslinked network. The glass transition temperature, Tg, is a function of the flexi-bility of the polymeric chains. If the flexibility decreases,the transition temperature increases. Flexibility is a func-tion of chain structure, crosslinked structure and crosslink density. For the hyperbranched polyesters the spherical shape of the molecules and the high crosslink density due to its high functionality decreases the flexibility of the cured films. Therefore, crosslinked hyperbranched polyester give higher glass transition temperature than crosslinked linear WO 96/07688 - ~ a 9 ~ 8 7 ~ ~ PCI~/SE9S/01013 oligomers as an effect of the structural difference.
The measurements made in the present invention were performed accordingly:
Molecular Weiqht Distribution Measurements of molecular weight distribution were performed on a WATERS 410 GPC system equipped with a WISP 712 automated injector. The columns used were ~-Styragel of pore sized: 500, 105, 104, 103, and 100 Angstrom with polystyrene standards for calibration and tetrahydrofuran (THF) as sol-vent.
Dynamic Mechanical S~ectrosco~
The dynamic mechanical properties of the hyperbran-ched polyesters were measured by shear rheometry (Dynamic Analyser RDAII). Viscous liquid samples were ~m; ned at 25C
using two parallel plates of 12.5 mm radius with 0.62 to 0.76 ~m gap over a wide range of frequencies.
Flow Time Flow time of the resins with multifunctional mono-mer added was measured using a viscometric cup of number 68 for comparison of the viscosity of the hyperbranched polyesters with that of modified linear unsaturated polyester.
IR s~ectra Infra-red spectra of the polyesters at different reaction stages were recorded on a Perkin-Elmer Model 1710 Fourier Transform Spectrometer prepared as pressed KBr solid disk or smeared as an acetone solution of the resin on a NaCl prism to form a thin film.
Thermomechanical analysis Dynamic Mechanical Thermal Analyser (DMTA, Polymer ~aboratories MK II) was used to measure glass transition temperature (Tg) at the range of 40 to 250C and 1 Hz fre-quency of completely W cured films without TMPTA added.
W096/07688 . PCT/SE95/01013 oa9 9~7~
mixture of 15 ~ by weight of TMPTA and 85 ~ by weight of D-1, D-2 or D-3, the resultant resins were coated on a polyethylene terephtalate (PET) sheet. The test samples were cured in air on a conveyer belt with variable speed by W
irradiation for 0,15 seconds under a 300 W/in (120 W/cm) Model F300 D bulb (Fusion W Curing Systems) in the exposure chamber.
Example 5:
The procedure of Example 4 was repeated except that 100 parts of D-1, D-2 or D-3 polyesters are used instead of the mixture of the polyesters and TMPTA.
The irradiation time is varied by changing the speed of the conveyor belt. The polymerization rate of the hyperbranched polyester resins was determined by measuring the irradiation time required to obtain fully tack-free state for the cured film using a cotton bar. The data are given in Figure 9. The resin with oligomer D-3 needs the shortest curing time to get tack-free state.
The glass transition temperatures of the crosslin-ked (meth)acrylated hyperbranched polyesters D-1, D-2 and D-3 according to Example 5 from Dynamic Mechanical Thermal Analy-sis (DMTA) measurements are given in Figure 10. It can be seen that the glass transition temperature increases rapidly with increasing functionality of the cured hyperbranched oligomer.
The physical properties of the cured material are related to the structure of the crosslinked network. The glass transition temperature, Tg, is a function of the flexi-bility of the polymeric chains. If the flexibility decreases,the transition temperature increases. Flexibility is a func-tion of chain structure, crosslinked structure and crosslink density. For the hyperbranched polyesters the spherical shape of the molecules and the high crosslink density due to its high functionality decreases the flexibility of the cured films. Therefore, crosslinked hyperbranched polyester give higher glass transition temperature than crosslinked linear WO 96/07688 - ~ a 9 ~ 8 7 ~ ~ PCI~/SE9S/01013 oligomers as an effect of the structural difference.
The measurements made in the present invention were performed accordingly:
Molecular Weiqht Distribution Measurements of molecular weight distribution were performed on a WATERS 410 GPC system equipped with a WISP 712 automated injector. The columns used were ~-Styragel of pore sized: 500, 105, 104, 103, and 100 Angstrom with polystyrene standards for calibration and tetrahydrofuran (THF) as sol-vent.
Dynamic Mechanical S~ectrosco~
The dynamic mechanical properties of the hyperbran-ched polyesters were measured by shear rheometry (Dynamic Analyser RDAII). Viscous liquid samples were ~m; ned at 25C
using two parallel plates of 12.5 mm radius with 0.62 to 0.76 ~m gap over a wide range of frequencies.
Flow Time Flow time of the resins with multifunctional mono-mer added was measured using a viscometric cup of number 68 for comparison of the viscosity of the hyperbranched polyesters with that of modified linear unsaturated polyester.
IR s~ectra Infra-red spectra of the polyesters at different reaction stages were recorded on a Perkin-Elmer Model 1710 Fourier Transform Spectrometer prepared as pressed KBr solid disk or smeared as an acetone solution of the resin on a NaCl prism to form a thin film.
Thermomechanical analysis Dynamic Mechanical Thermal Analyser (DMTA, Polymer ~aboratories MK II) was used to measure glass transition temperature (Tg) at the range of 40 to 250C and 1 Hz fre-quency of completely W cured films without TMPTA added.
Claims (29)
1. Hyperbranched polyester of a polyol with 3 to 10 reactive hydroxyl groups, preferably of equivalent reactivity, and an aromatic polycarboxylic anhydride with 2 to 4 carboxyl groups, preferably 3 carboxyl groups, each hydroxyl group of the polyol forming an ester linkage with one anhydride group of the polycarboxylic anhydride, and further glycidyl (meth)acrylate or allyl glycidyl ether forming ester linkages with the remaining carboxyl groups of the anhydride and free hydroxyl groups.
2. Hyperbranched polyester of a polyol with 3 to 10 reactive hydroxyl groups, preferably of equivalent reactivity, and an aromatic polycarboxylic anhydride with 2 to 4 carboxyl groups, preferably 3 carboxyl groups, each hydroxyl group of the polyol forming an ester linkage with one anhydride group of the polycarboxylic anhydride, and glycidyl (meth)acrylate or allyl glycidyl ether forming ester linkages with the remaining carboxyl groups of the anhydride and free hydroxyl groups, and further (meth)acrylic anhydride and/or an aliphatic carboxylic anhydride forming ester linkages with the free hydroxyl groups.
3. Hyperbranched polyester obtainable by a process comprising the following steps:
a) reacting an aromatic polycarboxylic anhydride with 2 to 4 carboxyl groups, preferably 3 carboxyl groups, with a polyol with 3 to 10 reactive hydroxyl groups, preferably of equivalent reactivity, in the presence of an activating agent, the amount of anhydride being at least one mole of anhydride per hydroxyl group in the polyol, b) reacting the product from a) with glycidyl (meth)acrylate or allyl glycidyl ether in an amount at least corresponding to one mole of glycidyl (meth)acrylate or allyl glycidyl ether per free carboxylic acid group of the product of a).
a) reacting an aromatic polycarboxylic anhydride with 2 to 4 carboxyl groups, preferably 3 carboxyl groups, with a polyol with 3 to 10 reactive hydroxyl groups, preferably of equivalent reactivity, in the presence of an activating agent, the amount of anhydride being at least one mole of anhydride per hydroxyl group in the polyol, b) reacting the product from a) with glycidyl (meth)acrylate or allyl glycidyl ether in an amount at least corresponding to one mole of glycidyl (meth)acrylate or allyl glycidyl ether per free carboxylic acid group of the product of a).
4. Hyperbranched polyester according to claim 3, characterized in that activating agent is present in a catalytic amount.
5. Hyperbranched polyester according to claim 3, characterized in that the activating agent is SnCl2.
6. Hyperbranched polyester obtainable by a process comprising the steps a) and b) of claim 3 and the further step:
c) the product from step b) is further reacted with (meth)acrylic anhydride in an amount sufficient to esterify a part or all of the free hydroxyl groups of the product from step b).
c) the product from step b) is further reacted with (meth)acrylic anhydride in an amount sufficient to esterify a part or all of the free hydroxyl groups of the product from step b).
7. Hyperbranched polyester obtainable by a process comprising the steps a) and b) of claim 3 or the steps a), b) and c) from claim 6 and the further step that the product from step b) or c) is further reacted with an aliphatic carboxylic anhydride in an amount to esterify a part of or all of the remaining hydroxyl groups of the products.
8. Hyperbranched polyester according to claims 2, 6 and 7, characterized in that the (meth)acrylic anhydride and the aliphatic carboxylic anhydride forming ester linkages with the free hydroxyl groups is methacrylic anhydride and acetic anhydride.
9. Hyperbranched polyester according to any of claims 1 to 8, characterized in that the polyol is pentaerythritol and the aromatic polycarboxylic anhydride is 1,2,4-benzenetricarboxylic anhydride and the glycidyl(meth)acrylate is glycidyl acrylate.
10. Hyperbranched polyester according to any of claims 1 to 9, characterized in that the hyperbranched polyester is a dendritic polyester or a crosslinked dendritic polyester.
11. A process for the production of a hyperbranched polyester, characterized in that it comprises the following steps:
a) reacting an aromatic polycarboxylic anhydride with 2 to 4 carboxyl groups, preferably 3 carboxyl groups, with a polyol with 3 to 10 reactive hydroxyl groups, preferably of equivalent reactivity, in the presence of an activating agent, the amount of anhydride being at least one mole of anhydride per hydroxyl group in the polyol, b) reacting the product from a) with glycidyl (meth)acrylate or allyl glycidyl ether in an amount at least corresponding to one mole of glycidyl (meth)acrylate or allyl glycidyl ether per free carboxylic acid group of the product of a).
a) reacting an aromatic polycarboxylic anhydride with 2 to 4 carboxyl groups, preferably 3 carboxyl groups, with a polyol with 3 to 10 reactive hydroxyl groups, preferably of equivalent reactivity, in the presence of an activating agent, the amount of anhydride being at least one mole of anhydride per hydroxyl group in the polyol, b) reacting the product from a) with glycidyl (meth)acrylate or allyl glycidyl ether in an amount at least corresponding to one mole of glycidyl (meth)acrylate or allyl glycidyl ether per free carboxylic acid group of the product of a).
12. A process according to claim 11, characterized in that the activating agent is present in a catalytic amount.
13. A process according to claim 11, characterized in that the activating agent is SnCl2.
14. A process according to claim 11, characterized in that in step a) the reaction mixture is heated to a temperature below 100°C.
15. A process according to claim 11, characterized in that the amount of anhydride in step a) and of acrylate in step b) are in excess of the stated amount.
16. A process according to claim 11, characterized in that the reaction of step b) is made in the presence of a basic catalyst and an inhibitor for radical polymerization.
17. A process according to claim 16, characterized in that the basic catalyst is benzyldimethyldiamine.
18. A process according to claim 11, characterized in that it further comprises the following step:
c) the product from step b) is further reacted with (meth)acrylic anhydride in an amount sufficient to esterify a part or all of the free hydroxyl groups of the product from step b).
c) the product from step b) is further reacted with (meth)acrylic anhydride in an amount sufficient to esterify a part or all of the free hydroxyl groups of the product from step b).
19. A process according to claim 18, characterized in that the anhydride is methacrylic anhydride.
20. A process according to claims 11 or 18, characterized in that the product from step b) or c) is further reacted with an aliphatic carboxylic anhydride in an amount to esterify a part of or all of the remaining hydroxyl groups of the products.
21. A process according to claim 20, characterized in that the aliphatic carboxylic anhydride is acetic anhydride.
22. A process according to any of claims 11 to 21, characterized in that the polyol is pentaerythritol and the aromatic polycarboxylic anhydride is 1,2,4-benzene-tricarboxylic anhydride and the glycidyl(meth)acrylate is glycidyl acrylate.
23. A process according to any of claims 11 to 22, characterized in that the hyperbranched polyester is a dendritic polyester or a crosslinked dendritic polyester.
24. A curable resin characterized in that it comprises a hyperbranched polyester as defined in any of claims 1 to 10.
25. A curable resin according to claim 24, characterized in that it further comprises a photofragmenting initiator.
26. A curable resin according to claim 24 or 25, characterized in that it comprises a multifunctional monomer.
27. A curable resin according to claim 26 characterized in that the multifunctional monomer is trimethylolpropane triacrylate.
28. A curable resin according to any of claims 24 to 27, characterized in that it is curable with UV
irradiation.
irradiation.
29. Use of a curable resin according to any of claims 24 to 28 for the production of coatings, adhesives, laminates, foils and thin films and fibre-reinforced composites.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| SE9402994A SE503559C2 (en) | 1994-09-08 | 1994-09-08 | Radiation curable hyperbranched polyester, its method of preparation and its use |
| SE9402994-9 | 1994-09-08 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CA2198755A1 true CA2198755A1 (en) | 1996-03-14 |
Family
ID=20395166
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CA 2198755 Abandoned CA2198755A1 (en) | 1994-09-08 | 1995-09-08 | Radiation curable resins comprising hyperbranched polyesters |
Country Status (16)
| Country | Link |
|---|---|
| US (1) | US5834118A (en) |
| EP (1) | EP0779908B1 (en) |
| JP (1) | JP3459647B2 (en) |
| CN (1) | CN1070878C (en) |
| AT (1) | ATE187467T1 (en) |
| AU (1) | AU704344B2 (en) |
| CA (1) | CA2198755A1 (en) |
| DE (1) | DE69513840T2 (en) |
| DK (1) | DK0779908T3 (en) |
| ES (1) | ES2140704T3 (en) |
| GR (1) | GR3032356T3 (en) |
| NO (1) | NO311300B1 (en) |
| PT (1) | PT779908E (en) |
| RU (1) | RU2162861C2 (en) |
| SE (1) | SE503559C2 (en) |
| WO (1) | WO1996007688A1 (en) |
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| GB1481131A (en) * | 1974-03-22 | 1977-07-27 | Nat Starch Chem Corp | Actinic radiation curable materials |
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1994
- 1994-09-08 SE SE9402994A patent/SE503559C2/en not_active IP Right Cessation
-
1995
- 1995-09-08 DE DE1995613840 patent/DE69513840T2/en not_active Expired - Fee Related
- 1995-09-08 JP JP50943696A patent/JP3459647B2/en not_active Expired - Fee Related
- 1995-09-08 DK DK95931499T patent/DK0779908T3/en active
- 1995-09-08 PT PT95931499T patent/PT779908E/en unknown
- 1995-09-08 EP EP19950931499 patent/EP0779908B1/en not_active Expired - Lifetime
- 1995-09-08 ES ES95931499T patent/ES2140704T3/en not_active Expired - Lifetime
- 1995-09-08 CN CN95194947A patent/CN1070878C/en not_active Expired - Fee Related
- 1995-09-08 WO PCT/SE1995/001013 patent/WO1996007688A1/en active IP Right Grant
- 1995-09-08 AT AT95931499T patent/ATE187467T1/en not_active IP Right Cessation
- 1995-09-08 AU AU34893/95A patent/AU704344B2/en not_active Ceased
- 1995-09-08 RU RU97105770A patent/RU2162861C2/en not_active IP Right Cessation
- 1995-09-08 US US08/793,611 patent/US5834118A/en not_active Expired - Fee Related
- 1995-09-08 CA CA 2198755 patent/CA2198755A1/en not_active Abandoned
-
1997
- 1997-03-07 NO NO19971061A patent/NO311300B1/en not_active IP Right Cessation
-
2000
- 2000-01-13 GR GR20000400053T patent/GR3032356T3/en not_active IP Right Cessation
Also Published As
| Publication number | Publication date |
|---|---|
| SE503559C2 (en) | 1996-07-08 |
| RU2162861C2 (en) | 2001-02-10 |
| AU704344B2 (en) | 1999-04-22 |
| DE69513840D1 (en) | 2000-01-13 |
| AU3489395A (en) | 1996-03-27 |
| JP3459647B2 (en) | 2003-10-20 |
| ATE187467T1 (en) | 1999-12-15 |
| NO971061L (en) | 1997-04-30 |
| DK0779908T3 (en) | 2000-05-08 |
| NO311300B1 (en) | 2001-11-12 |
| SE9402994D0 (en) | 1994-09-08 |
| CN1070878C (en) | 2001-09-12 |
| US5834118A (en) | 1998-11-10 |
| ES2140704T3 (en) | 2000-03-01 |
| CN1163626A (en) | 1997-10-29 |
| SE9402994L (en) | 1996-03-09 |
| NO971061D0 (en) | 1997-03-07 |
| EP0779908B1 (en) | 1999-12-08 |
| GR3032356T3 (en) | 2000-04-27 |
| PT779908E (en) | 2000-05-31 |
| DE69513840T2 (en) | 2000-07-27 |
| EP0779908A1 (en) | 1997-06-25 |
| WO1996007688A1 (en) | 1996-03-14 |
| JPH10505377A (en) | 1998-05-26 |
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