WO1998045343A1 - An unsaturated polyester resin composition - Google Patents

An unsaturated polyester resin composition Download PDF

Info

Publication number
WO1998045343A1
WO1998045343A1 PCT/EP1998/001883 EP9801883W WO9845343A1 WO 1998045343 A1 WO1998045343 A1 WO 1998045343A1 EP 9801883 W EP9801883 W EP 9801883W WO 9845343 A1 WO9845343 A1 WO 9845343A1
Authority
WO
WIPO (PCT)
Prior art keywords
polyester resin
acid
resin composition
foam
polyester
Prior art date
Application number
PCT/EP1998/001883
Other languages
French (fr)
Inventor
Marzio Ligutti
Massimo Montecchi
Original Assignee
C.O.I.M. S.P.A. - Chimica Organica Industriale Milanese
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by C.O.I.M. S.P.A. - Chimica Organica Industriale Milanese filed Critical C.O.I.M. S.P.A. - Chimica Organica Industriale Milanese
Priority to AU73338/98A priority Critical patent/AU726612B2/en
Priority to EP98920494A priority patent/EP0971964A1/en
Priority to CA002296021A priority patent/CA2296021A1/en
Publication of WO1998045343A1 publication Critical patent/WO1998045343A1/en

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
    • C09D167/00—Coating compositions based on polyesters obtained by reactions forming a carboxylic ester link in the main chain; Coating compositions based on derivatives of such polymers
    • C09D167/06—Unsaturated polyesters having carbon-to-carbon unsaturation
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
    • C08F283/00—Macromolecular compounds obtained by polymerising monomers on to polymers provided for in subclass C08G
    • C08F283/01—Macromolecular compounds obtained by polymerising monomers on to polymers provided for in subclass C08G on to unsaturated polyesters

Definitions

  • the present invention relates to an unsaturated polyester resin composition, to its use for applications with foamed plastics materials and to articles comprising a core or layer of a foamed plastic material and a layer or coating obtained from said resin composition.
  • polyester adhesives can be employed for reparations, since it provides joint-less repairs.
  • Polyurethane adhesives would not readily enable such joint-less technique .
  • DE-A-12 36 187 describes protecting coatings for foamed polystyrene articles which are obtained by coating the polystyrene foam with a composition containing 25-75 percent by weight (% wt) of a polymerisable ethylenically unsaturated polyester and 25-75% wt of a polymerisable ethylenically unsaturated monomer of which 50 to 100% wt is an allyl- ether of N-methylol-urea or a derivative thereof.
  • JP-01319547-A describes moulded articles of polystyrene foam onto which an unsaturated polyester resin is applied; the process comprises coating and/or laminating together with a reinforcing material on a polystyrene foam a resin composition containing 100 parts by weight of unsaturated polyester resin and 5-200 parts by weight of a compound, such as di-cyclo-pentenyl oxy ethyl acrylate or di-cyclo- pentenyl oxy ethyl meth-acrylate .
  • JP-63260936-A describes a composite material comprising a core foam material, such as polystyrene foam and a radical polymerised composition impregnated in the core foam; the composition comprises an unsaturated polyester resin, a cross-linking agent, a curing promoting agent and a curing agent; the cross-linking agent is a monofunctional acryl monomer or a multifunctional acryl monomer.
  • JP-49021428-A describes a coating composition for thermoplastic mouldings, particularly of polystyrene foam comprising an unsaturated resin and a monoester from (meth) acrylic acid and a C 2 -C 8 polyol or a C 4 -C 18 ether linkage- containing polyol, or the reaction product of a C 2 -C 18 alkylene oxide and (meth) acrylic acid, such as particularly 2-hydroxyethyl acrylate.
  • styrene monomer can be used as a co-solvent for the unsaturated polyester together with the above-mentioned compounds, as shown by the working examples, even relatively low amounts of styrene in combination with 2-hydroxy ethyl acrylate caused at least partial erosion of the polystyrene foam.
  • a partial erosion of the polystyrene foam takes place with the use of a composition comprising about 60% wt of polyester resin and about 32% wt of hydroxy ethyl acrylate (HEA) and as little as about 8% wt of styrene monomer.
  • HSA hydroxy ethyl acrylate
  • polyester resin composition which contains lower amounts of monomeric styrene without impairing the mechanical properties thereof and which does not dissolve polystyrene foam or styrene-based copolymer foams. It would also be desirable to have coated and/or bonded articles including a foam core or layer, wherein the foam does not undergo surface degradation or chemical attack when in contact with a polyester resin.
  • a first object of the present invention is to provide an improved polyester resin composition which does not dissolve polystyrene foam or styrene-based copolymer foams or in general polymers obtained from the polymerisation of ethylenically unsaturated monomers.
  • Another object of the invention is to provide a polyester resin composition having a reduced amount of styrene monomer, without impairing the mechanical properties of the cured polyester resin.
  • Still another object of the invention is to provide coated and/or bonded articles including a core or layer of a styrene polymer or copolymer foam or in general polymers ob- tained from the polymerisation of ethylenically unsaturated monomers and a coating of an unsaturated polyester resin, wherein the foam does not undergo surface degradation or chemical attack and/or delamination as a result of a contact with the polyester resin.
  • a further object of the invention is to provide a process for coating foams of styrene polymers or copoly-mers or in general polymers obtained from the polymerisation of ethylenically unsaturated monomers with a layer of polyester resin having structural properties or for bonding sheets, such as GRP sheet or plywood sheets, to said polymers by means of a polyester-based adhesive.
  • Still another object is to provide a polyester resin composition which allows application on foamed materials without causing unacceptable styrene-monomer emissions in the working environment.
  • the present invention offers new perspectives to all of the above-described problems .
  • polystyrene-based foam for making articles by bonding sheets, by way of an unsaturated polyester resin composition results in better workability as there is no dust creation during cutting operations of polystyrene- based foams. Further, polystyrene foam is mechanically recyclable, while polyurethane is not; this improves the end product and the manufacturing process from the environmental point of view.
  • the present invention offers even more opportunities to improve the properties of the manufactured articles, because the mechanical properties of extruded polystyrene are superior than those of polyurethane of equal den- sity. This means that articles that have a constructive aspect/role have either an improved performance, or can be optimised.
  • extruded polystyrene foam hardly takes up any water, is to a very high degree resistant to moisture and has a very high resistance to a broad range of chemicals. This results in a superior long term performance of the articles made thereof (e.g. a refrigerated truck body, an insulated container, a pontoon) .
  • the polyester resin composition comprises, as the monomeric solvent, styrene and an hydroxy alkyl acrylate or methacrylate in a defined ratio with respect to the amount of unsaturated polyester.
  • the invention provides an unsaturated polyester resin composition
  • values of the above mentioned ratio lower than 0.12 do not provide a suitable chemical bonding of the polyester onto the styrene polymer or copolymer foam whereas values higher than 0.18 cause an at least partial surface degradation and/or dissolution of the foam; preferred values for the above ratio are between 0.16 to 0.18.
  • polyester resin compositions including an amount of polyester varying in a wide range, preferably from 65% wt to 80% wt and more preferably between 65% and 75% wt, referred to the total amount of unsaturated polyester and monomeric solvent.
  • the amount of monomeric solvent in the composition is preferably from 35 to 20% wt and more preferably from 35 to 25% wt.
  • the amount of styrene monomer in the monomeric solvent is preferably from 10 to 16% wt referred to the amount of polyester and monomeric solvent.
  • the amount of styrene in said polyester resin composition is increased, for example by 1% wt, correspondingly, the amount of hydroxy alkyl (meth) -acrylate is to be increased in the amount of 5.55% wt to 8.33% wt, in order to provide a polyester resin composition which does not detrimentally affect the surface of the styrene polymer or copolymer foam or in general polymers obtained from the polymerisation of ethylenically unsaturated monomers .
  • the unsaturated polyester in the composition is preferably the product of esterification of a glycol, an unsaturated dicarboxylic acid or anhydride and optionally a saturated dicarboxylic acid or anhydride; preferably, in the presence of a chain termination agent which is preferably an allyl ether of a C3-C 10 polyol, most preferably a diallyl ether of C 3 -C 10 aliphatic or cycloaliphatic polyol, such as giycerol, trimethylol propane or ethane.
  • a chain termination agent which is preferably an allyl ether of a C3-C 10 polyol, most preferably a diallyl ether of C 3 -C 10 aliphatic or cycloaliphatic polyol, such as giycerol, trimethylol propane or ethane.
  • Suitable glycols comprise ethylene glycol, diethylene gly ⁇ col, tri-ethylene glycol, polyethylene glycol, propylene glycol, di-propylene glycol, tri-propylene glycol, polypropylene glycol, 2,2-di-methylpropane diol, 1,3-butane diol, 1,2-butylene glycol, 2,3-butylene glycol.
  • the unsaturated acid or anhydride is preferably maleic or fumaric acid or anhydride; however, also itaconic acid and chloromaleic acid or anhydride may conveniently be used. Mixtures of different unsaturated acid or anhydrides may also be used.
  • the saturated acid or anhydride when used, is preferably selected from the group consisting of phthalic acid, tetra- hydrophthalic acid, cyclohexane dicarboxylic acid, adipic acid, sebacic acid, succinic acid, azelaic acid, isophtha- lic acid, terephthalic acid and the corresponding anhydrides, HET acid and chlorendic anhydride and mixtures thereof.
  • glycol is used with respect to the overall amount of the acid, such as preferably a 5 to 20% molar excess.
  • the chain termination agent is preferably trimethylol propane diallyl ether.
  • the unsaturated polyester of the present invention typically has an acid unsaturation index, expressed as the ratio between the number of equivalents of unsaturated acid in the polyester and the total number of equivalents of acid in said polyester, higher than 0.50, more preferably not lower than 0.70, and most preferably not lower than 0.85.
  • the average numerical molecular weight (Mn) of the polyester is preferably from 800 to 1400; and the average weight molecular weight (Mw) is preferably from 1800 to 2300.
  • the polyester resin composition has preferably an overall percentage of unsaturations , expressed as the ratio between the total number of unsaturated moles in the composition (polymer plus solvent) and the total number of moles from which the polyester resin composition is obtained, from 0.55 to 0.75.
  • the polyester resin composition has preferably an acid number of from 30 to 50 mg KOH/ml, an hydroxyl number of from
  • the polyester resin composition of the present invention may further comprise additives which are usually present in conventional unsaturated polyester resin compositions, such as inhibitors, storage stabilisers, curing promoters and inorganic fillers.
  • inhibitors are hydroquinone and toluene hydroquinone.
  • Preferred promoters are the so- called metal soaps, such as cobalt, copper or vanadium oc-rank, naphthenate and acetonate.
  • the resin composition of the present invention is cured by means of the already known unsaturated polyester resin curing methods, preferably by means of peroxide initiators, such as particularly methyl-ethyl-ketone (MEK) peroxide and methyl isobutyl ketone peroxide.
  • peroxide initiators such as particularly methyl-ethyl-ketone (MEK) peroxide and methyl isobutyl ketone peroxide.
  • MEK methyl-ethyl-ketone
  • a typical curing system consists of 0.2% wt cobalt octoate (6% wt Co), 2% wt of a MEK-MEK peroxide solution (50% by weight for each component in the solution), referred to 100 grams polyester resin composition.
  • the resin composition has preferably a curing time of from 8 to 15 minutes, a gel time of from 10 to 90 minutes and an exothermic peak of about 150-170°C.
  • the preferred use of the resin composition of the present invention is for coating the surface of foamed articles.

Landscapes

  • Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Wood Science & Technology (AREA)
  • Macromonomer-Based Addition Polymer (AREA)
  • Laminated Bodies (AREA)

Abstract

An unsaturated polyester resin composition is disclosed, comprising an unsaturated polyester and a monomeric solvent reactive with said polyester, characterised in that the monomeric solvent comprises styrene and hydroxy alkyl acrylate or methacrylate, wherein alkyl is C1 to C4 and wherein the amounts of styrene, hydroxy alkyl (meth)acrylate and unsaturated polyester in said composition comply with the equation (I) in parts by weight. The composition is particularly useful for coating or bonding foamed articles, particularly foamed polystyrene.

Description

An unsaturated polyester resin composition
The present invention relates to an unsaturated polyester resin composition, to its use for applications with foamed plastics materials and to articles comprising a core or layer of a foamed plastic material and a layer or coating obtained from said resin composition.
More particularly, the invention relates to a polyester resin composition comprising an unsaturated polyester and a monomeric solvent which is cross-reactive with said polyester.
Conventional unsaturated polyester resin compositions include relatively high amounts of ethylenically unsaturated monomeric solvents, particularly styrene-based monomeric solvents. The relatively high amount of styrene makes such compositions unsuitable for coating polystyrene foamed plastics materials or generally foamed polymers including styrene as a co-monomer, since the styrene-based solvent attacks and dissolves the polymer containing styrene.
Polystyrene foam is a widely used rigid plastic material; in many cases it is used as an insulation material, in other cases it is used for its structural properties combined with its chemical and water resistance. In many applications, the foam core needs to be covered by a protective layer; reasons therefor might be the need for high impact resistance, fire regulations, improving the long term weathering properties and/or aesthetic reasons. This is the case, for example, in insulated trailers, insulated containers and buoyancy applications.
There are applications where foamed plastics materials, such as polyurethane, are coated with unsaturated polyester resin or are bonded using unsaturated polyester to a plastics or wood material. In this type of application, there are basically two problems, one relating to the polyurethane (i) and one related to the unsaturated polyester resin (ii) .
(i) Polyurethane is not always the most appropriate material for many of these applications. In applications, such as refrigerated transport, the insulation is subject to high moisture loads. However, polyurethane is known to be highly moisture sensitive.
In the past, tests have been carried out on insulated truck bodies or trailers which had been in use for several years. These tests showed that the polyurethane foam cores were soaked with water, while the extruded polystyrene cores still were practically dry. It is obvious that the insulation value of the wet polyurethane cores was reduced substantially and, thus, did not meet the requirements anymore.
(ii)The unsaturated polyester resins typically employed have a high styrene monomer content (35 to 45% wt); this causes high styrene monomer contents in the manufacturing halls creating an unhealthy working environment. The high styrene monomer contents in the working environment cannot be reduced unless manufacturing process is changed or unless the manufacturing units are restructured including the necessary evacuation units. The use of such evacuation units is not economically feasible in most cases.
There are currently applications where extruded polystyrene foam is used as a core for articles wherein the bonding is carried out by using a polyurethane-based adhesive. How- ever, using a polyester resin as adhesive, instead of poly- urethane-based adhesive results in several advantages, one being the fact that polyester resin bonds are less rigid bonds which results in a good mechanical performance to vibrations and dynamic loads . Especially in insulated transport applications this improves the long term performance of the articles.
Another advantage of using polyester resin as adhesive is that polyester adhesives can be employed for reparations, since it provides joint-less repairs. Polyurethane adhesives, however, would not readily enable such joint-less technique .
Furthermore, previous attempts to provide articles including a core of polystyrene foam and a structural surface coating made from conventional unsaturated polyester resin compositions or bonded articles comprising a layer of polystyrene foam and an unsaturated polyester resin sheet reinforced with glass fibres (GRP) bonded to said layer by means of an unsaturated polyester-based glue were unsuccessful, due to the attack of the polystyrene surface by the relatively high amounts of styrene monomer.
DE-A-12 36 187 describes protecting coatings for foamed polystyrene articles which are obtained by coating the polystyrene foam with a composition containing 25-75 percent by weight (% wt) of a polymerisable ethylenically unsaturated polyester and 25-75% wt of a polymerisable ethylenically unsaturated monomer of which 50 to 100% wt is an allyl- ether of N-methylol-urea or a derivative thereof.
JP-01319547-A describes moulded articles of polystyrene foam onto which an unsaturated polyester resin is applied; the process comprises coating and/or laminating together with a reinforcing material on a polystyrene foam a resin composition containing 100 parts by weight of unsaturated polyester resin and 5-200 parts by weight of a compound, such as di-cyclo-pentenyl oxy ethyl acrylate or di-cyclo- pentenyl oxy ethyl meth-acrylate .
JP-63260936-A describes a composite material comprising a core foam material, such as polystyrene foam and a radical polymerised composition impregnated in the core foam; the composition comprises an unsaturated polyester resin, a cross-linking agent, a curing promoting agent and a curing agent; the cross-linking agent is a monofunctional acryl monomer or a multifunctional acryl monomer.
JP-49021428-A describes a coating composition for thermoplastic mouldings, particularly of polystyrene foam comprising an unsaturated resin and a monoester from (meth) acrylic acid and a C2-C8 polyol or a C4-C18 ether linkage- containing polyol, or the reaction product of a C2-C18 alkylene oxide and (meth) acrylic acid, such as particularly 2-hydroxyethyl acrylate. Whereas styrene monomer can be used as a co-solvent for the unsaturated polyester together with the above-mentioned compounds, as shown by the working examples, even relatively low amounts of styrene in combination with 2-hydroxy ethyl acrylate caused at least partial erosion of the polystyrene foam.
According to the examples, a partial erosion of the polystyrene foam takes place with the use of a composition comprising about 60% wt of polyester resin and about 32% wt of hydroxy ethyl acrylate (HEA) and as little as about 8% wt of styrene monomer.
It is reported that when HEA is used as the only monomeric solvent, the surface of polystyrene foam does not appear to be substantially eroded; it has been found however that the use of HEA as the only monomeric solvent causes substantial increase of the curing time necessary to achieve the desirable mechanical properties of the polyester coating and a post-curing treatment appears to be required which is undesirable. An increase of the curing temperature in order to reduce the curing time is not advisable, since higher curing temperatures, such as 70-80°C, would be detrimental to foamed plastics materials, in particular polystyrene foams.
Therefore, it would be highly desirable to provide an improved polyester resin composition which contains lower amounts of monomeric styrene without impairing the mechanical properties thereof and which does not dissolve polystyrene foam or styrene-based copolymer foams. It would also be desirable to have coated and/or bonded articles including a foam core or layer, wherein the foam does not undergo surface degradation or chemical attack when in contact with a polyester resin.
Thus, a first object of the present invention is to provide an improved polyester resin composition which does not dissolve polystyrene foam or styrene-based copolymer foams or in general polymers obtained from the polymerisation of ethylenically unsaturated monomers.
Another object of the invention is to provide a polyester resin composition having a reduced amount of styrene monomer, without impairing the mechanical properties of the cured polyester resin.
Still another object of the invention is to provide coated and/or bonded articles including a core or layer of a styrene polymer or copolymer foam or in general polymers ob- tained from the polymerisation of ethylenically unsaturated monomers and a coating of an unsaturated polyester resin, wherein the foam does not undergo surface degradation or chemical attack and/or delamination as a result of a contact with the polyester resin.
A further object of the invention is to provide a process for coating foams of styrene polymers or copoly-mers or in general polymers obtained from the polymerisation of ethylenically unsaturated monomers with a layer of polyester resin having structural properties or for bonding sheets, such as GRP sheet or plywood sheets, to said polymers by means of a polyester-based adhesive.
Still another object is to provide a polyester resin composition which allows application on foamed materials without causing unacceptable styrene-monomer emissions in the working environment.
The present invention offers new perspectives to all of the above-described problems .
Being able to use polystyrene-based foam for making articles by bonding sheets, by way of an unsaturated polyester resin composition results in better workability as there is no dust creation during cutting operations of polystyrene- based foams. Further, polystyrene foam is mechanically recyclable, while polyurethane is not; this improves the end product and the manufacturing process from the environmental point of view.
Secondly, the present invention offers even more opportunities to improve the properties of the manufactured articles, because the mechanical properties of extruded polystyrene are superior than those of polyurethane of equal den- sity. This means that articles that have a constructive aspect/role have either an improved performance, or can be optimised.
Another aspect of the present invention is that extruded polystyrene foam hardly takes up any water, is to a very high degree resistant to moisture and has a very high resistance to a broad range of chemicals. This results in a superior long term performance of the articles made thereof (e.g. a refrigerated truck body, an insulated container, a pontoon) .
According to the invention, it has been found that such objects are achieved when the polyester resin composition comprises, as the monomeric solvent, styrene and an hydroxy alkyl acrylate or methacrylate in a defined ratio with respect to the amount of unsaturated polyester.
Accordingly, the invention provides an unsaturated polyester resin composition comprising an unsaturated polyester and a monomeric solvent reactive with said polyester, characterised in that the monomeric solvent comprises styrene and a hydroxy alkyl methacrylate or acrylate, wherein alkyl is Ci to C4 and wherein the amount of styrene, hydroxyalkyl (meth)-acrylate and unsaturated polyester in said composition comply with the following equation in parts by weight: (I) Styrene (parts wt) = 0 12 - 0 18
Polyester (parts wt) + hydroxy alkyl (meth) - acrylate (parts wt)
It has been found that values of the above mentioned ratio lower than 0.12 do not provide a suitable chemical bonding of the polyester onto the styrene polymer or copolymer foam whereas values higher than 0.18 cause an at least partial surface degradation and/or dissolution of the foam; preferred values for the above ratio are between 0.16 to 0.18.
The teaching of the invention allows to provide polyester resin compositions including an amount of polyester varying in a wide range, preferably from 65% wt to 80% wt and more preferably between 65% and 75% wt, referred to the total amount of unsaturated polyester and monomeric solvent. Correspondingly, the amount of monomeric solvent in the composition is preferably from 35 to 20% wt and more preferably from 35 to 25% wt. The amount of styrene monomer in the monomeric solvent is preferably from 10 to 16% wt referred to the amount of polyester and monomeric solvent. According to the teaching of the invention, if the amount of styrene in said polyester resin composition is increased, for example by 1% wt, correspondingly, the amount of hydroxy alkyl (meth) -acrylate is to be increased in the amount of 5.55% wt to 8.33% wt, in order to provide a polyester resin composition which does not detrimentally affect the surface of the styrene polymer or copolymer foam or in general polymers obtained from the polymerisation of ethylenically unsaturated monomers .
The unsaturated polyester in the composition is preferably the product of esterification of a glycol, an unsaturated dicarboxylic acid or anhydride and optionally a saturated dicarboxylic acid or anhydride; preferably, in the presence of a chain termination agent which is preferably an allyl ether of a C3-C10 polyol, most preferably a diallyl ether of C3-C10 aliphatic or cycloaliphatic polyol, such as giycerol, trimethylol propane or ethane.
Suitable glycols comprise ethylene glycol, diethylene gly¬ col, tri-ethylene glycol, polyethylene glycol, propylene glycol, di-propylene glycol, tri-propylene glycol, polypropylene glycol, 2,2-di-methylpropane diol, 1,3-butane diol, 1,2-butylene glycol, 2,3-butylene glycol.
The unsaturated acid or anhydride is preferably maleic or fumaric acid or anhydride; however, also itaconic acid and chloromaleic acid or anhydride may conveniently be used. Mixtures of different unsaturated acid or anhydrides may also be used.
The saturated acid or anhydride, when used, is preferably selected from the group consisting of phthalic acid, tetra- hydrophthalic acid, cyclohexane dicarboxylic acid, adipic acid, sebacic acid, succinic acid, azelaic acid, isophtha- lic acid, terephthalic acid and the corresponding anhydrides, HET acid and chlorendic anhydride and mixtures thereof.
Usually, a slight molar excess of glycol is used with respect to the overall amount of the acid, such as preferably a 5 to 20% molar excess.
The chain termination agent, is preferably trimethylol propane diallyl ether.
The unsaturated polyester of the present invention typically has an acid unsaturation index, expressed as the ratio between the number of equivalents of unsaturated acid in the polyester and the total number of equivalents of acid in said polyester, higher than 0.50, more preferably not lower than 0.70, and most preferably not lower than 0.85.
The average numerical molecular weight (Mn) of the polyester is preferably from 800 to 1400; and the average weight molecular weight (Mw) is preferably from 1800 to 2300. The polyester resin composition has preferably an overall percentage of unsaturations , expressed as the ratio between the total number of unsaturated moles in the composition (polymer plus solvent) and the total number of moles from which the polyester resin composition is obtained, from 0.55 to 0.75.
The polyester resin composition has preferably an acid number of from 30 to 50 mg KOH/ml, an hydroxyl number of from
Figure imgf000012_0001
The polyester resin composition of the present invention may further comprise additives which are usually present in conventional unsaturated polyester resin compositions, such as inhibitors, storage stabilisers, curing promoters and inorganic fillers. Preferred inhibitors are hydroquinone and toluene hydroquinone. Preferred promoters are the so- called metal soaps, such as cobalt, copper or vanadium oc- toate, naphthenate and acetonate.
The resin composition of the present invention is cured by means of the already known unsaturated polyester resin curing methods, preferably by means of peroxide initiators, such as particularly methyl-ethyl-ketone (MEK) peroxide and methyl isobutyl ketone peroxide. A typical curing system consists of 0.2% wt cobalt octoate (6% wt Co), 2% wt of a MEK-MEK peroxide solution (50% by weight for each component in the solution), referred to 100 grams polyester resin composition. The resin composition has preferably a curing time of from 8 to 15 minutes, a gel time of from 10 to 90 minutes and an exothermic peak of about 150-170°C.
The preferred use of the resin composition of the present invention is for coating the surface of foamed articles.

Claims

The foamed materials on which the resin composition can be applied include polystyrene foam (extruded and expanded), syndiotactic polystryrene, styrene copolymer foams, such as ABS, polyurethane foam, polyethylene terephtalate (PET) foam, polypropylene foam, polyethylene foam, polyphenyl ether foam and polyvinyl chloride (PVC) foam. The application is carried out by means of conventional methods, such as brushing, rolling, spraying or dipping and other existing known methods. The coating layer may have a thickness higher than 1 mm and preferably in the range of from 2 to 5 mm. After application the coating layer is cured according to conventional methods . The curing temperature is typically with the range of from 15°C (ambient temperature) to 50°C.Additionally, the polyester resin composition according to the invention may be used as an adhesive in order to bond sheets of conventional unsaturated polyester resin to the surface of said foamed articles . The temperature of the press plates, within which the resin composition is cured, may range between 30°C and 60°C. The preferred temperature of the press plates is between 30°C and 40°C.Furthermore, the polyester resin composition of the present invention can be used as a primer coating of foamed articles which can then be either coated or bonded with any conventional unsaturated polyester resin. Accordingly, the invention comprises within its scope articles comprising a core or layer made of a foamed material and at least one layer (either as a coating or as an adhesive) obtained from the polyester resin composition of the present invention.Also comprised within the scope of the invention are articles as above defined having an additional primer coating layer consisting of the polyester resin composition of the present invention which is applied between the surface of said foamed core and any conventional unsaturated polyester resin (either used as a coating or an adhesive).The resin composition may also be used to manufacture composite materials, wherein the polyester resin composition according to the invention is reinforced by fabric, mats and/or fibres.Preferred applications of the polyester resin composition of the present invention are for manufacturing sandwich panels having a core of polystyrene foam, such as panels for thermally insulated trailers or containers. The polyester resin composition of the present invention is also suitable to manufacture coated parts for marine applications, such as pontoons.Example 1 - PREPARATION OF POLYESTER RESIN COMPOSITION 12.55 parts by weight of propylene glycol, 24.25 parts by weight dipropylene glycol, 7.04 parts by weight phthalic anhydride, 8.9 parts by weight trimethylol propane diallyl ether, 31.99 parts by weight fumaric acid, 0.01 parts by weight hydroquinone are charged into a reactor equipped with a mixer, a partial condenser and a shielding gas system. The esterification reaction is carried out under nitrogen gas flow by the conventional fusion method at a temperature of from 175 to 180°C by periodically checking the viscosity into the reactor, until the acid value of the polyester resin has value from 36 to 47 mg KOH/ml. The reaction product was then cooled to 150°C and discharged into a dilutor vessel containing 15 parts by weight styrene and 12 parts by weight hydroxy-ethyl-methacrylate and 0.002 part by weight copper naftenate (6%), while taking care that the internal temperature in the dilutor vessel is not higher than 80°C .The obtained polyester resin composition has a polyester polymer content of about 74% wt. The polyester has an acid unsaturation index of 85%.Tests were carried out in order to confirm that the polyester resin composition of the present invention could be applied onto a polystyrene foam and to check the compatibility, i.e., chemical attack (Example 2) and the tensile bond strength (Example 3) of polystyrene sandwich panels.In all the tests, the polyester resin composition was cured with a curing system consisting of 0.2% wt of cobalt octo- ate (6% wt Co) and 2% wt of a MEK-MEK peroxide solution (50% by weight for each component in the solution), referred to 100 grams polyester resin.Example 2 - COMPATIBILITYIn a first series of laboratory tests, the compatibility of the polyester resin of this invention with the polystyrene foam was evaluated as follows: a first set of samples (Combination 2A) was prepared, wherein the polyester resin composition of Example 1, to which the curing system has been added, was poured on top of a STYROFOAM* RTM polystyrene board (Trademark of The Dow Chemical Company) and distributed uniformly by means of a brush, in order to obtain a layer having a thickness of 2-4 mm. After curing of the polyester resin at ambient temperature(about 25°C), a hardened layer of polyester bonded to the polystyrene surface was obtained.According to the same procedure, another two sets of samples were made, one combining the STYROFOAM* RTM polystyrene with the commercially available polyester resins (EXTER 102S available from COIM S.p.A.) (Combination 2B) and one combining the polyester resin of the invention (Example 1) with polyurethane having a density of 40 kg/m3 (Combination 2C). Visual comparison between the 3 combinations showed that on the set of samples of the Combinations 2A and 2C there was no chemical attack or dissolution and the surface coating was smooth.In addition, the coating layer was removed from the foam of each of the above-described three combinations. Visual inspection and comparison showed again that the surface had not been chemically attacked in the Combinations 2A and 2C, and had not degraded, which was the case in the Combination 2B.Example 3 - BONDING PROPERTIESAnother series of tests was carried out in order to measure the bonding properties and to prove the technical feasibility of the coating process. These tests were carried out by bonding a 2 mm GRP sheet (manufactured by General Plast, Italy) to a foam core by using the unsaturated polyester resin of the present invention. Approximately 1 kg of resin was used per square meter resulting in a 1 mm thick coating layer.The tensile bonding strength and the tensile modulus were measured according to ASTM D-1623. The shear bonding strength and the shear modulus were measured according to ASTM C-273.A set of samples was prepared for each foam type, i.e. polystyrene foam and polyurethane foam. The polystyrene foam used was an extruded polystyrene foam STYROFOAM* RTM, (♦trademark of The Dow Chemical Company), having a density of 40 kg/m3 (set 3A) and was coated with the unsaturated polyester resin of Example 1. For comparison purposes, a polyurethane foam was coated with a commercially available unsaturated polyester resin (EXTER 102S from COIM S.p.A.) (set 3B). The polyurethane used was a 40 kg/m3 density rigid polyurethane foam commercially available.In all samples, the foam cores were 50 mm thick. Curing was done under a pressure of 0.5 kg/cm2 and at 50°C.Average tensile bonding strength values measured on samples according to the present invention (set 3A) were: 424 kPa; and the shear bonding strength tests gave shear bonding strengths of 354 kPa.The measurements on the polyurethane foam samples (set 3B) gave: tensile bonding strength of 337 kPa and the shear strength of 210 kPa.Example 4 - BONDING VS. COATINGFurther mechanical tests were carried out to confirm the above tests and to compare the bonding technique to the coating technique.For this purpose, one set of samples comprising extruded polystyrene foam STYROFOAM* RTM were bonded to a 2 mm GRP sheet (commercially available from General Plast, Italy) using the polyester resin of the invention (set 4A) and another set of samples comprising said polystyrene foam were coated with a 3 mm thick layer of the polyester resin of the present invention (set 4B) . The bonded samples were cured under pressure (0.5 kg/cm2) and at 50°C. The coated samples were cured at room temperature under pressure (0.5 kg/cm2 ) . For the bonded samples (set 4A) , the average tensile bonding strength was of 650 kPa, and the average shear strength was of 493 kPa and the average shear modulus was of 5,836 kPa.For the coated samples (set 4B), the average tensile bonding strength = 600 kPa, the average shear strength = 513 kPa and average shear modulus = 6,219 kPa.The tests also show that the invention applied on extruded polystyrene foam having a density of 40 kg/ provides results typically 30 to 50 percent better than the results obtained by the existing techniques applied on polyurethane rigid foam also having a density of 40 kg/m . CLAIMS
1. An unsaturated polyester resin composition comprising an unsaturated polyester and a monomeric solvent reactive with said polyester, characterised in that the monomeric solvent comprises styrene and hydroxy alkyl acrylate or methacrylate, wherein alkyl is Ci to C and wherein the amounts of styrene, hydroxy alkyl (meth) acrylate and unsaturated polyester in said composition comply with the following equation in parts by weight: (I)
St -y-.rene ( -£p_arts wt) = 0 /1 -0 1R
Polyester (parts wt) + hydroxy alkyl (meth) - acrylate (parts wt)
2 . A composition according to Claim 1, wherein the unsaturated polyester is the product of esterification of a glycol, at least an unsaturated dicarboxylic acid or anhydride, optionally a saturated dicarboxylic acid or anhydride and a chain termination agent consisting of an allyl ether of a C3-C10 polyol.
3. A composition according to Claim 2, wherein said unsaturated dicarboxylic acid or anhydride is selected from the group consisting of maleic acid or anhydride, fumaric acid or anhydride, itaconic acid and chloromaleic acid or anhydride and mixtures thereof.
4. A composition according to Claim 2, wherein said unsaturated acid or anhydride is selected from the group consisting of phthalic acid or anhydride, tetra-hydrophthalic acid or anhydride, cyclohexane dicarboxylic acid or anhydride, adipic acid, sebacic acid, succinic acid, azelaic acid, isophthalic acid, terephthalic acid or anhydrides, HET acid, chlorendic anhydride and mixtures thereof.
5. A composition according to Claim 2, wherein said chain termination agent is trimethylol propane diallyl ether.
6. A composition according to Claim 1, wherein said glycol is selected from the group consisting of ethylene glycol, diethylene glycol, tri-ethylene glycol, polyethylene glycol, propylene glycol, di-propylene glycol, tri-propylene glycol, polypropylene glycol, 2,2-di-methylpropane diol, 1,3-butane diol, 1,2-butylene glycol, 2,3-butylene glycol and mixtures thereof.
7. A composition according to any of Claims 1-6, wherein the unsaturated polyester has an acid unsaturation index, expressed as the ratio between the number of equivalents of unsaturated acid in the polyester and the total number of equivalents of acid in said polyester higher than 0.50.
8. A composition according to any of Claims 1-7, wherein the unsaturated polyester has an acid unsaturation index not lower than 0.70.
9. A composition according to any of Claims 1 to 8, wherein the polyester has an acid unsaturation index not lower than 0.85.
10. A composition according to any of Claims 1 to 9, wherein the polyester resin composition has an overall percentage of unsaturations, expressed as the ratio between the total number of unsaturated moles in the composition (polymer plus solvent) and the total number of moles from which the resin composition is obtained, from 0.55 to 0.75.
11. A composition according to any of the preceding Claims, wherein the resin composition has an acid number of from 30 to 50 mg KOH/ml, and a hydroxyl number of from 50 to 105 mg
12. A composition according to any of the preceding Claims, comprising from 65 to 80% wt of unsaturated polyester and from 35 to 20% wt of monomeric solvent.
13. A composition according to any of the preceding Claims, comprising from 10 to 16% wt styrene referred to the overall composition.
14. A composition according to any of the preceding Claims, comprising inhibitors selected from hydroquinone and toluene hydroquinone.
15. A composition according to any of the preceding Claims, further comprising curing promoters and/or fillers.
16. An unsaturated polyester resin composition according to the preceding Claims, wherein the ratio according to equation (I) is of from 0.16 to 0.18.
PCT/EP1998/001883 1997-04-04 1998-04-01 An unsaturated polyester resin composition WO1998045343A1 (en)

Priority Applications (3)

Application Number Priority Date Filing Date Title
AU73338/98A AU726612B2 (en) 1997-04-04 1998-04-01 An unsaturated polyester resin composition
EP98920494A EP0971964A1 (en) 1997-04-04 1998-04-01 An unsaturated polyester resin composition
CA002296021A CA2296021A1 (en) 1997-04-04 1998-04-01 An unsaturated polyester resin composition

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
ITTO97A000286 1997-04-04
IT97TO000286 IT1291705B1 (en) 1997-04-04 1997-04-04 COMPOSITION OF UNSATURATED POLYESTER RESIN.

Publications (1)

Publication Number Publication Date
WO1998045343A1 true WO1998045343A1 (en) 1998-10-15

Family

ID=11415617

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/EP1998/001883 WO1998045343A1 (en) 1997-04-04 1998-04-01 An unsaturated polyester resin composition

Country Status (5)

Country Link
EP (1) EP0971964A1 (en)
AU (1) AU726612B2 (en)
CA (1) CA2296021A1 (en)
IT (1) IT1291705B1 (en)
WO (1) WO1998045343A1 (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20110020570A1 (en) * 2009-07-02 2011-01-27 Innovative Energy, Inc. Materials and processes for fabricating containers and containers formed therewith
EP2882809A4 (en) * 2012-08-10 2016-01-20 Henkel IP & Holding GmbH Method for improving adhesion of polyurethane adhesive to polyester based laminate without surface preparation

Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR2366330A1 (en) * 1976-10-02 1978-04-28 Hoechst Ag ACRYLIC RESIN COPOLYMER SOLUTIONS, PROCESS FOR THE PREPARATION OF THE SAME AND USE OF THE SAME IN REACTIVE LACQUERS

Patent Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR2366330A1 (en) * 1976-10-02 1978-04-28 Hoechst Ag ACRYLIC RESIN COPOLYMER SOLUTIONS, PROCESS FOR THE PREPARATION OF THE SAME AND USE OF THE SAME IN REACTIVE LACQUERS

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20110020570A1 (en) * 2009-07-02 2011-01-27 Innovative Energy, Inc. Materials and processes for fabricating containers and containers formed therewith
EP2882809A4 (en) * 2012-08-10 2016-01-20 Henkel IP & Holding GmbH Method for improving adhesion of polyurethane adhesive to polyester based laminate without surface preparation

Also Published As

Publication number Publication date
IT1291705B1 (en) 1999-01-21
ITTO970286A1 (en) 1998-10-04
CA2296021A1 (en) 1998-10-15
AU726612B2 (en) 2000-11-16
EP0971964A1 (en) 2000-01-19
AU7333898A (en) 1998-10-30

Similar Documents

Publication Publication Date Title
US6114402A (en) Modified rigid, foamable urethane composition and method
EP1124877B1 (en) Unsaturated polyester resin and the use of it
EP0700419B1 (en) Process for preparing a fiber-reinforced composite and molded articles made therefrom
US5549969A (en) Enhanced surface for glass fiber reinforced plastics
US4529757A (en) Thermosetting resin patching compound
AU726612B2 (en) An unsaturated polyester resin composition
AU729258B2 (en) Foamed articles with unsaturated polyester resin coating and process for their manufacture
US4038342A (en) Low profile additives in polyester systems
US4347170A (en) Unsaturated polyester compositions and their use
KR100201802B1 (en) Low profile additive based on asymmetric glycols and aromatic diacids for polyester resin systems
AU551772B2 (en) Patching compound
JP4149059B2 (en) Radical polymerizable resin composition
JP3294809B2 (en) Lightweight laminate
WO1995009202A1 (en) Additives to improve surface characteristics of unsaturated polyester molding composition
CA1159188A (en) Unsaturated polyester compositions and their use
JPS61287935A (en) Damping material
JP2005179388A (en) Curable resin composition, method for producing the same and method for utilizing the same resin composition
JPH0584759A (en) Thermosetting resin composition for in-mold coating molding and coated molded product
JPH04146913A (en) Resin composition, and coating material and molding material comprising same
JPS61287934A (en) Damping material
JP2004338209A (en) Laminated molded article and method for producing the same
JPS6115898B2 (en)

Legal Events

Date Code Title Description
AK Designated states

Kind code of ref document: A1

Designated state(s): AL AM AT AU AZ BA BB BG BR BY CA CH CN CU CZ DE DK EE ES FI GB GE GH GM GW HU ID IL IS JP KE KG KP KR KZ LC LK LR LS LT LU LV MD MG MK MN MW MX NO NZ PL PT RO RU SD SE SG SI SK SL TJ TM TR TT UA UG US UZ VN YU ZW

AL Designated countries for regional patents

Kind code of ref document: A1

Designated state(s): GH GM KE LS MW SD SZ UG ZW AM AZ BY KG KZ MD RU TJ TM AT BE CH CY DE DK ES FI FR GB GR IE IT LU MC NL PT SE BF BJ CF CG CI CM GA GN ML MR NE SN TD TG

DFPE Request for preliminary examination filed prior to expiration of 19th month from priority date (pct application filed before 20040101)
121 Ep: the epo has been informed by wipo that ep was designated in this application
WWE Wipo information: entry into national phase

Ref document number: 1998920494

Country of ref document: EP

WWE Wipo information: entry into national phase

Ref document number: 73338/98

Country of ref document: AU

WWE Wipo information: entry into national phase

Ref document number: 09402249

Country of ref document: US

ENP Entry into the national phase

Ref document number: 2296021

Country of ref document: CA

Ref country code: CA

Ref document number: 2296021

Kind code of ref document: A

Format of ref document f/p: F

WWP Wipo information: published in national office

Ref document number: 1998920494

Country of ref document: EP

REG Reference to national code

Ref country code: DE

Ref legal event code: 8642

NENP Non-entry into the national phase

Ref country code: JP

Ref document number: 1998542345

Format of ref document f/p: F

WWG Wipo information: grant in national office

Ref document number: 73338/98

Country of ref document: AU

WWW Wipo information: withdrawn in national office

Ref document number: 1998920494

Country of ref document: EP