AU715162B2 - Recyclable molded high modulus fiber reinforced thermoplastic structures and process for preparing the same - Google Patents
Recyclable molded high modulus fiber reinforced thermoplastic structures and process for preparing the same Download PDFInfo
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- AU715162B2 AU715162B2 AU19093/97A AU1909397A AU715162B2 AU 715162 B2 AU715162 B2 AU 715162B2 AU 19093/97 A AU19093/97 A AU 19093/97A AU 1909397 A AU1909397 A AU 1909397A AU 715162 B2 AU715162 B2 AU 715162B2
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- 229920005989 resin Polymers 0.000 claims description 23
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- 238000000034 method Methods 0.000 claims description 20
- 239000000758 substrate Substances 0.000 claims description 20
- 239000000463 material Substances 0.000 claims description 13
- 239000002131 composite material Substances 0.000 claims description 12
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- 229920000139 polyethylene terephthalate Polymers 0.000 claims description 10
- 239000005020 polyethylene terephthalate Substances 0.000 claims description 10
- 239000012783 reinforcing fiber Substances 0.000 claims description 10
- 239000003365 glass fiber Substances 0.000 claims description 9
- 239000000203 mixture Substances 0.000 claims description 9
- 239000003973 paint Substances 0.000 claims description 7
- 229920000728 polyester Polymers 0.000 claims description 6
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 claims description 5
- 238000010438 heat treatment Methods 0.000 claims description 4
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- 210000000329 smooth muscle myocyte Anatomy 0.000 description 5
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- 239000000853 adhesive Substances 0.000 description 4
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- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 2
- 229920001634 Copolyester Polymers 0.000 description 2
- OWYWGLHRNBIFJP-UHFFFAOYSA-N Ipazine Chemical compound CCN(CC)C1=NC(Cl)=NC(NC(C)C)=N1 OWYWGLHRNBIFJP-UHFFFAOYSA-N 0.000 description 2
- 229920002292 Nylon 6 Polymers 0.000 description 2
- 239000004696 Poly ether ether ketone Substances 0.000 description 2
- 239000003963 antioxidant agent Substances 0.000 description 2
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- 239000000378 calcium silicate Substances 0.000 description 2
- 229910052918 calcium silicate Inorganic materials 0.000 description 2
- OYACROKNLOSFPA-UHFFFAOYSA-N calcium;dioxido(oxo)silane Chemical compound [Ca+2].[O-][Si]([O-])=O OYACROKNLOSFPA-UHFFFAOYSA-N 0.000 description 2
- 230000032798 delamination Effects 0.000 description 2
- 239000011152 fibreglass Substances 0.000 description 2
- 239000004615 ingredient Substances 0.000 description 2
- 238000010422 painting Methods 0.000 description 2
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- 229920001652 poly(etherketoneketone) Polymers 0.000 description 2
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- 238000002360 preparation method Methods 0.000 description 2
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 2
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- 239000004925 Acrylic resin Substances 0.000 description 1
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- JHWNWJKBPDFINM-UHFFFAOYSA-N Laurolactam Chemical compound O=C1CCCCCCCCCCCN1 JHWNWJKBPDFINM-UHFFFAOYSA-N 0.000 description 1
- 229920000571 Nylon 11 Polymers 0.000 description 1
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- 239000002033 PVDF binder Substances 0.000 description 1
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- 239000004698 Polyethylene Substances 0.000 description 1
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- 239000003677 Sheet moulding compound Substances 0.000 description 1
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 1
- 239000006096 absorbing agent Substances 0.000 description 1
- 230000002411 adverse Effects 0.000 description 1
- 229920000180 alkyd Polymers 0.000 description 1
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- 230000033228 biological regulation Effects 0.000 description 1
- 229910000019 calcium carbonate Inorganic materials 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 239000006229 carbon black Substances 0.000 description 1
- 239000003054 catalyst Substances 0.000 description 1
- 210000004027 cell Anatomy 0.000 description 1
- 239000004927 clay Substances 0.000 description 1
- 229910052570 clay Inorganic materials 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 238000013329 compounding Methods 0.000 description 1
- XCJYREBRNVKWGJ-UHFFFAOYSA-N copper(II) phthalocyanine Chemical compound [Cu+2].C12=CC=CC=C2C(N=C2[N-]C(C3=CC=CC=C32)=N2)=NC1=NC([C]1C=CC=CC1=1)=NC=1N=C1[C]3C=CC=CC3=C2[N-]1 XCJYREBRNVKWGJ-UHFFFAOYSA-N 0.000 description 1
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- JEIPFZHSYJVQDO-UHFFFAOYSA-N iron(III) oxide Inorganic materials O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 0.000 description 1
- VTHJTEIRLNZDEV-UHFFFAOYSA-L magnesium dihydroxide Chemical compound [OH-].[OH-].[Mg+2] VTHJTEIRLNZDEV-UHFFFAOYSA-L 0.000 description 1
- 239000000347 magnesium hydroxide Substances 0.000 description 1
- 229910001862 magnesium hydroxide Inorganic materials 0.000 description 1
- 239000000395 magnesium oxide Substances 0.000 description 1
- CPLXHLVBOLITMK-UHFFFAOYSA-N magnesium oxide Inorganic materials [Mg]=O CPLXHLVBOLITMK-UHFFFAOYSA-N 0.000 description 1
- AXZKOIWUVFPNLO-UHFFFAOYSA-N magnesium;oxygen(2-) Chemical compound [O-2].[Mg+2] AXZKOIWUVFPNLO-UHFFFAOYSA-N 0.000 description 1
- 239000004005 microsphere Substances 0.000 description 1
- 239000006082 mold release agent Substances 0.000 description 1
- 229920001778 nylon Polymers 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 229920002647 polyamide Polymers 0.000 description 1
- 229920001230 polyarylate Polymers 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 229920001155 polypropylene Polymers 0.000 description 1
- 229920002981 polyvinylidene fluoride Polymers 0.000 description 1
- 239000012779 reinforcing material Substances 0.000 description 1
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- OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 description 1
- 229920006337 unsaturated polyester resin Polymers 0.000 description 1
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Landscapes
- Reinforced Plastic Materials (AREA)
Description
P/00/011 Regulation 3.2
AUSTRALIA
PATENTS ACT 1990 COMPLETE SPECIFICATION FOR A STANDARD PATENT
ORIGINAL
S.
*J*
ft S. e r TO BE COMPLETED BY APPLICANT S.
S
I PDNtS m Name of Applicant: Actual Inventor(s): Address for Service: Invention Title: John Michael Fisher; Edward Hatchadoorian CALLINAN LAWRIE, 278 High Street, Kew, 3101, Victoria, Australia "RECYCLABLE MOLDED HIGH MODULUS FIBER REINFORCED THERMOPLASTIC STRUCTURES AND PROCESS FOR PREPARING THE SAME" The following statement is a full description of this invention, including the best method of performing it known to me:- 24/4/97LP9178.CS,1
A
RECYCLABLE MOLDED 11IGH MODULUS FIBER REINFORCED THERMOPLASTIC
STRUCTURES
AND PROCESS FOR PREPARIN~G THE SAME FIELD OF THE INVENTION The present invention relates to providing recyclable high modulus fiber reinforced composite structures having an enhanced surface appearance.
BACKGROUND OF THE INVENTION The use of plastic components in combination with metal parts is common in the production of automobiles. Mixtures of resins and reinforcing materials are used as sheet molding compounds, SMCs, which are molded to form. various shaped articles. Generally in applications requiring high quality painted surfaces, highly filled thermosetting SMCs have been used.' A long standing problem in providing reinforced composite structures resides in manufacturing structures which when painted provide a Class A finish.
These structures such as automotive body panels must be capable of being processed in assembly plants with steel panels. They must be able to survive assembly plant conditions, painting and baking, where maximum metal temperatures can reach 200*C for as long as 30 minutes with surface coatings remai ning firmly adherred to the substrate and retaining their Class A :appearance. The body panels must have, after processing,, an appearance that is comparable to the appearance of an adjoining part made of steel.
They must also have acceptable dimensional stability in order to maintain the highest quality fit and finish over wide temperature extremes found in various geographical market segments. When using SMCs, surface appearance problems such as "paint pops' occur due to emission of low molecular weight monomers in the thermosetting substrate, In addition an ever increasing concern is whether the material is readily recyclable during manufacture and in post manufacture use. For example, can the resin component be remelted or depolymerized. The thermosetting SMCs are not recyclable in the sense that they cannot be remelted or depolymerized.
la- SUMMARY OF THE INVENTION The products of this invention which solve the problems noted above are made by preparing composite structures comprised of a substrate prepared from a plurality of layers on a self-supporting porous web comprised of randomly dispersed high modulus reinforcing fibers held together by solidified thermoplastic resin. The layers are heated to provide a premold form which is then placed in a mold to flow, solidify, and substantially crystallize the thermoplastic resin. The resulting reinforced thermoplastic substrate is coated in the mold with a thin coating of a thermosetting resin-containing composition.
In preparing the composite structures of the invention, the layers of o• porous web are stacked together to form a batt which is heated in a convection oven to convert the batt into a moldable form. The number of layers is determined by weighing the precut shapes to provide a predetermined mold charge mass which is based on the final desired molded part thickness. The ••go moldable form is then placed in a heated mold. The mold is closed and pressure is applied to flow mold the preform to form a consolidated part and to
*S
substantially crystallize the thermoplastic resin component.
Complete crystallization of the thermoplastic resin may occur but is not essential to achieve the invention.
I/8/96LP7810.PGSI -2- Upon completion of the molding operation, the mold halves are separated and/or the pressure is released to permit introduction of a thermosetting resincontaining coating material. The mold is then closed, and under pressure, the material spreads over the surface of the molded preform. Heating under pressure is continued for a time sufficient to set the coating composition.
Surprisingly, the thermosetting composition adheres tenaciously to the reinforced molded thermoplastic substrate and exhibits outstanding surface appearance.
The batts used to prepare the preforms are comprised of from 5 to 0 50 percent by weight glass fibers and from 50 to 95 percent by weight thermoplastic resin. The batts are air permeable and are made from air permeable webs of randomly dispersed high modulus fibers held together at fiber crossover locations by solidified globules of thermoplastic resin enveloping the fibers at the crossover locations. Some of the randomly dispersed fibers have bead-like drops of solidified thermoplastic resin adhered thereto at locations along their length at locations other than at crossovers. The preparation of such webs is disclosed in Geary and Weeks 244/e97LP9178.PGS.2 3 US Patent Application No. 07/606,651, fied October 31, 1990 and European Patent Application 0 341 977, published November 15, 1989.
The products of this invention are composite structures which are warp-free, have very smooth surfaces and exhibit excellent physical properties. Thle thermosetting resin-containing surface coating strongly adheres to the reinforced molded thermoplastic substrate surface. When the structures are used in automotive body panels and inted, the painted surface is rated Class The quality of the surfac,.; coating can be measured using a commercially available distinctness of image (DOI) meter.
Reflected light intensity from a photo detector is measured as a function of the scatterlng angle. If the scattering function is short and wide, the surface is said to have a low DOI. If the scattering is limited, the surface has a high DOI. DOI meters detect the reflected light in a region slightly away from the spectral angle. If the light detected is small, the distinctness is high. DOI is 15 measured on.a scale from 0 to 100 with 100 being the highest level of smoothness.
Painting procedures which are well known in the art may be used with the structures of this invention. They may be painted side by side with steel parts. For example, the surfaces may be primed and topcoa _j o~r optionally a basecoat/clear coat finish may be applied. When placed a drying oven after being painted, no "paint pops' occur whereas in usin& SMCs, due to emission of low molecular weight monomers, "paint pops" are encountered.
BRIEF DESCRIPTION OF THE DRAWINGS :25 FIG. 1 is a schematic illustration of a cross section of a composite structure produced by the process of this invention.
DETAILED DESCRIPTON OF THE INVETIN Referring to the drawing, Fig. 1 shows reinforced thermoplastic substrate 10 which has been coated with thermosetting resin-containing coating 12. The resulting composite part is coated with multiple layers of paint 14.
In carrying out the process of the invention, a porous batt is formed from an intimate homogenous blend of reinforcing fiber and thermoplastic resin fiber components. The reinforcing fiber may be any high modulus fiber, such as polyarnides, glass, carbon, polyesters and high temperature nylons. A modulus of at least 100,000 M Pascals is preferred.
The reinforcing fibers may be of consistent length or a mixture of variable length fibers. Generally, long fibers in the range of one to eight centimeters are preferred.
The thermoplastic resin fibers may be any thermoplastic or combination of several suitable thermoplastics for the application. Examples of suitable thermoplastics include, but are not limited to, polyethylene, polypropylene, polyesters, copolyesters, polyamides, including Nylon 6, Nylon 6/6, Nylon 11, Nylon 12, and J2, polyetheretherketone (PEEK), polyetherketoneketone (PEKK), polymethylphenylene, polyarylates and polyvinylidene fluoride. The denier and length of the thermoplastic fiber is chosen such that the volume of a single fiber is within a range, preferably between 1.5 x 10- 4 to 10 x 10-3 mm 3 which when heated results in a globule volume in the range of approximately 0.5 x 10 4 to 1 x 10-3 mm 3 Given the volume range, the thermoplastic fiber diameter is generally chosen based on 15 economic considerations. For instance, the most economical polyester staple is 1.5 denier per filament (DPF). In general, a length of 1-50 mm and DPF of greater than 0.5 is preferred.
An intimately blended web if formed from the high modulus and thermoplastic fibers. The basis weight of the formed web is in the range 20 of 0.05 0.2 pounds per square foot (0.244 0.98 kg/sq The formed web is passed through a convection heating oven to dry and melt the thermoplastic fiber forming globules which bond the structure together. This melting step produces a web of substantial strength sufficient for normal web handling and is critical to obtaining a web that has the high porosity desired 25 for subsequent convection heating in preparation for molding.
The thermosetting resin-containing coating compositions are unsaturated resins which are rendered insoluble and infusible by crosslinking. Such resins are well known in the art and can be of the type disclosed by Sorenson and Campbell in Chapter 7, "Synthetic Resins", 3 0 published by INTERSCIENCE PUBLISHERS, INC., New York, 1961.
Examples include polyester/acrylic/vinyl monomer resins. The various combinations of polyester, acrylic and vinyl monomers are very great. Also various alkyd and unsaturated polyester resins described in MODERN PLASTICS ENCYCLOPEDIA, 1989 Edition,published by Mc Graw Hill, New York, may be used.
The thermosetting coating compositions can be filled or compounded to give the desired viscosity and flow characteristics for molding and to afford the desired physical properties in the resulting coating.
Examples of such fillers or compounding ingredients are fillers like clay, talc, magnesium oxide, magnesium hydroxide, calcium carbonate and calcium silicate, mold release agents, colorants such as red iron oxide, titanium oxide, carbon black, organic color pigments such as phthalocyanine blue or green, antidegradants, UV absorbers, calcium silicate, hollow glass or resin microspheres, thickening agents, inhibitors and the like. Care should be exercised in the use of high filler contents as this may give high viscosities and result in flow and handling difficulties.
A preferred thermosetting resin-containing composition consists of a styrene containing modified acrylic resin mixture which is sold by GenCorp Inc. under the trademark Genglaze®.
A preferred reinforcing fiber used in the invention is glass fiber which consists of conventional spun glass strand having a diameter between and 50 microns and a cut length of 1 to 8 cm. As is common in the industry, such glass is sized and chopped to length and shipped "wet" in moisture proof containers to the customer. A preferred material is that sold by Owens- Coming Fiberglass (OCF) under the label 133A.
The preferred molding method for practicing the invention is compression molding. A stack of sheets are layered together. The stack is placed in a forced air convection oven and heated above the melting point of the thermoplastic resin component for less than one minute. The heated preform is then placed in a compression mold where the tool temperature is adjusted to a temperature to crystallize the thermoplastic resin component.
Sufficient pressure is applied to flow mold the preform to fill out the mold.
After a dwell time of preferably 30 to 60 seconds the mold is opened. As soon as possible after opening the mold, a thermosetting resin-containing component is introduced into the mold in an amount sufficient to create a layer from 3 to 10 mils (0.076 to 0.254 mm) thick over the upper surface of the preform. The coated structure is held in the mold under pressure for a time sufficient to cure the thermosetting resin-containing component. The coated structure is permitted to cool sufficiently for handling and is then removed from the mold.
In compression molding the mold must be opened enough to place the charge of coating composition in the mold on the surface to be coated. In another type of molding, such as injection molding, the mold is opened enough to insert the charge means, i.e. opening it by an amount equal to the desired thickness of the coating, to permit injection of the component, or injection may be made against the pressure in the mold.
In a preferred embodiment of the process of this invention, a porous web of the type described above comprised of glass fiber and polyethylene terephthalate (PET) fiber is precut into a predetermined shape.
Several layers of the precut material, (15-25 layers) are stacked together to make up a molding charge. The molding charge is then placed in a specially designed convection oven where the thermoplastic resin is remelted. The preheating is accomplished with an air temperature of from 285 -320°C and requires 30-90 seconds. The flow (velocity) of heated air through the charge 15 is in the range from 150 to 400 feet per minute (45.72 to 121.92 meters per minute) which for an average thickness mold charge will create a pressure drop through the thickness of the charge of less than 7 inches of water.
After the resin is remelted, the molding charge is removed from the oven and placed in a compression mold. The mold surface temperature is typically between 150-175°C when using polyethylene terephthalate resin. The charge size is typically between 40 and 100% of the planform area of the part to be molded. As the mold closes on the molding charge, a tool presssure of 2000 psi (13.8 M pascals) or greater should be achieved which is typically maintained through the duration of the part forming step. Mold dwell is typically 30-60 seconds depending on the thickness of the part.
Upon completion of the part forming step, surface enhancement is achieved through use of in-mold-coating using a thermosetting resin-containing material. As disclosed above, the coating can be done manually or by automated injection.
In the manual operation, the mold halves are separated upon completion of the part forming process. It is essential at this stage that the surface of the molded part be free of debris, e.g. molding flash. The in-moldcoating is premixed with a catalyst and then poured onto the part surface to be coated. The amount of coating used is typically 0.06 to 0.22 grams per square inch (0.0093 to 0.0341 gm,/sqcm) of part surface to be coated. This 7 will give a coating thickness from 3 to 10 mils (0.076 to 0.254 mm). The mold is then closed, and a tool pressure of not more than 1000 psi (6.9 M pascals), 500-800 psi is optimal, (3.5 M 5.5 M pascals) is achieved. This tool pressure flows the in-mold coating over the surface of the molded part. The mold dwell is 15-60 seconds depending on the particular coating system used. The mold is then opened, and the part is removed.
The composite part can be assembled with steel parts and painted using well known procedures. Among the many suitable paint compositions which may be used are those disclosed in U.S. Patents to 4,816,500, U.S.4,954,559 and U.S.5,051,209..
In the automated process, upon completion of the part forming step, the pressure is relieved, and the mold halves are separated slightly.
Precatalyzed coating composition is then injected through an injector port across the surface of the tool. Again, the same rule for the amount of coating applies. Immediately after injection, the mold is closed to a tool pressure of not more than 1000 psi (6.9 M pascals), and the mold dwell time is again eoeeo 60 seconds depending on the particular type of coating composition used.
The mold is then opened and the part removed.
The process of the invention can be used to mold automobile 20 parts such as grille and headlamp assemblies, deck hoods, fenders, door panels and roofs as well as in the manufacture of various plastic articles such as food trays, appliance and electrical components and in other applications where surface smoothness is required for subsequent application of paint.
The in-mold-coated products of this invention are recyclable.
2 5 The properties of recovered thermoplastic products are not adversely affected by the presence of the thermosetting resin-containing coatings.
The invention will be further illustrated by the following examples in which parts and percentages are by weight unless otherwise indicated. Units reported throughout the specification and claims in SI units have been converted from the English system to the SI System.
EXAMPLES
EXAMPLE 1 A self-supporting porous batt was prepared from polyethylene terephthalate fiber (PET) having an as spun denier of 1.5. The fiber was covened to a staple length of 1/4 inch (0.635 cm) and intimately mixed with 1 inch long glass fiber having a diameter of about 0.5 mil (0.013 mm). The 8 above ingredients were slurried in water and directed to a moving belt from a paper machine head box, then to a dryer. The mat consisted of 40.7 Wt. glass fiber (Owens Coming Fiberglass 57.2 Wt. PET fiber and 9.1 Wt. of a lower melting copolyester binder fiber Ciba Geigy's antioxidant, Irganox91010, was added to the slurry in an amount of 1.0 Wt. A belt speed of 22 fpm (6.71 mpm) and heater temperature of 195C was used to partially melt the PET fiber. A batt having a basis weight of about 0.171 lb/sqft (8.35 kq/sqcm) and a consistency of 0.54 Wt. was obtained.
The batt was placed in a convection oven and heated at a temperature of 285°C for 30 seconds while circulating hot air through the batt at about 350 feet per minute (106.68 m/min) to melt the PET component. The batt was then placed in a compression mold for 1 minute at a temperature of 150-180°C to crystallize the structure. Mold pressure was controlled at between 1,500 and 2,500 psi (10.34 and 17.24 M pascals). The 15 mold was opened to expose the exterior surface of the molded structure.
As soon as possible after opening the mold, a thermosetting styrene containing modified acrylic resinous coating material sold by GenCorp Inc. under the trademark GENGLAZE ®EC 600 was applied to the exposed surface of the molded structure in an amount of 0.14 20 gram/square inch (217.95 gm/sqm) The mold was reclosed under partial vacuum at a lower pressure of about 200 to 1000 psi (1.4 to 6.9 M pascals) to distribute the coating material over the surface of the molded structure.
After 60 seconds, the mold was opened and the coated structure was removed. The coating was uniformly distributed, having a thickness of 6 25 mils, with a very smooth surface EXAMPLE 2 The procedure described in Example 1 was repeated except that the glass fiber content of the batt was reduced to 25 wt. no binder fiber was used, the polyethylene terephthalate fiber content was increased to 75 wt. and Ciba Geigy's antioxidant, Irganox®1330, was used in an amount of 0.25 wt. the belt speed was increased to 25 fpm (7.62 m/m) and the heater temperature was increased to 280 0 C. The sheet, having a basis weight of 0.091 lb/sqft (0.444 kg/sqm).
A clicker die was used to convert the rolled batt into a form suitable for thermal compression molding. A preform consisting of twenty sheets stacked as a batt gave a part weight of about 1.0 to 1.5 Ibs/sqft (0.488 to 0.732 gm/sqcm) on thermal compression molding.
Before thermal compression molding, the batt was placed in a convection oven and hot air was circulated through the batt at about 350 ft/min (106.68 m/min) for 30 seconds at 285°C to convert the porous batt into a moldable form. The pliable melt was placed into a mold for one minute at a mold temperature of 150 to 180'C to produce a crystallized structure. The mold pressure was controlled at 2000 psi (13.8 M pascals).
As soon as possible after opening the mold, a resinous coating material consisting of GENGLAZE® EC 600 was applied to the exposed surface of the molded structure in an amount of 0.14 grams/sq inch (217.95 gn/sqm). The mold was reclosed under partial vacuum at a lower pressure S• of about 200 to 1000 psi (1.4 to 6.9 M pascals) to distribute the coating material over the surface of the molded structure. After 60 seconds the mold 15 was opened, and the coated structure was removed. The coating had a thickness of 6 mils (0.152mm) A very smooth coated surface was obtained.
Products prepared by the process of this invention were tested using a Bendix Surface Profilometer, Model No. 21, stylus head Bendix T-231 and probe diameter of 0.0004 inch (0.01016 mm) to determine the surface roughness. Products of this invention were found to have a maximum surface roughness deviation of less than 50 micro-inches (0.00127 mm) over a 0.25 inch (6.35 mm) span.
Adhesion of the thermosetting resin-containing coating to the thermoplastic substrate was tested using an Instron tensile tester. Two metal cylinders having a diameter of 1.596 inches (4.05 cm),2 sq inches surface area,(12.9 sqcm) were bonded using Dexter Hysol® adhesive, EA 934NA, a two part past adhesive, to each side of a test sample. When the adhesive was cured, the pieces were pulled apart in the Instron tester. The test samples were prepared by the process described in the Examples. The results of the tests are set forth in the following Table:
MATERIAL
Sample 1
STRENGTH
(psi) (M pascals 2452 16.9 Sample 2 Sample 3 2379 2810 2480 16.4 19.4 17.1 TYPE OF FAILURE Coating separated from the substrate Coating separated from the substrate Delamination of the substrate Delamination of the Substrate Sample 4 (Painted) S. *5S *555
*SSS
For purposes of defining this invention, the term "adhesion value means the tensile strength of the bond between the surface coating and 15 the substrate as measured using an Instron tensile tester, Model No.1127, using a 25,000 kg reversible load cell, or equivalent, and reported in psi (pascals). Products of this invention have adhesion values greater than 1000 psi (6.9 M pascals). This adhesion value must be attained to provide an acceptable product which is useful in industry applications. In conducting 2 0 tests to determine adhesion values any suitable adhesive which has a bonding strength greater than the force required to delaminate the substrate may be used.
Where the terms "comprise", "comprises", "comprised" or "comprising" are used in this specification, they are to be interpreted as specifying the presence of the stated features, integers, steps or components referred to, but not to preclude the presence or addition of one or more other feature, integer, step, component or group thereof.
0 0* 0 :00.00 0* 0 0 0* *0 o* oo* 17/12/97VSAP9178.SPE,10a
Claims (7)
1. A process for preparing a recyclable reinforced composite structure having enhanced surface appearance comprising heating a batt comprised of a plurality of layers of a self- supporting porous web comprised of randomly dispersed high modulus reinforcing fiber held together by solidified thermoplastic resin to convert the batt into a moldable form; placing the moldable form into a heated mold and flowing said moldable form under pressure to substantially crystallize the thermoplastic resin component. introducing a thermosetting resin-containing coating material into the mold adjacent at least one surface of the crystallized structure by 00 separating the sections of said mold and/or releasing the pressure and closing ooe°oo said heated mold under pressure to provide a substantially uniform coating on said one surface. 0 0 dwelling the coated structure in the mold for a time sufficient to set said coating material, and 0 0: recovering a molded part having an enhanced surface 20 appearance.
2. The process of Claim 1 wherein said thermoplastic resin is a polyester.
3. The process of Claim 1 or Claim 2, wherein said high modulus reinforcing fiber is glass fiber comprising from 5 to 50 percent by weight of said moldable form.
4. The process of Claim 3 wherein said glass fiber has a length from 1 to 10 cm and a diameter from 5 to 50 microns and said thermoplastic resin is polyethylene terephthalate. 17/08/99,a191 78.clm,1 1 Ila- A composite structure prepared according to the process of any one of Claims 1 to 4, having a substrate comprised of high modulus reinforcing fibers randomly dispersed in a thermoplastic resin and a thin thermosetting resin-containing coating adhered to a surface of said substrate, said thermoplastic resin being in a substantially crystallized state, said coating having a very smooth surface that when painted produces a Class A rated surface and said coating adherring strongly to the surface of said substrate.
6. A composite structure prepared according to the process of any one of Claims 1 to 4, having a substrate comprised of high modulus reinforcing fibers randomly dispersed in a thermoplastic resin and a thin thermosetting resin-containing coating adhered to a surface of said
12- substrate, said thermoplastic resin being in a substantially crystallized state, said coating having a maximum surface roughness deviation of less than 50 micro- inches (0.00127mm) over a 0.25 inch (6.35mm) span for the coated surface and a coating to substrate adhesion value greater than 1000psi (6.9 M pascals). 7. The structure of Claim 6 wherein said coating has a thickness from about 0.076 to 0.26mm. 8. The structure of Claim 7 wherein said reinforcing fiber is glass fiber and said thermoplastic resin is a polyester resin. 9. The structure of Claim 8 wherein said thermosetting resin is an acrylic based vinyl polymer composition. 10. The structure of Claim 8 having multiple layers of paint on the surface of said thin thermosetting resin-containing coating. 11. The use of the composite structure according to any one of 4 4. 4* 4* io 4 4* 4. 4444 4* 4 4 Claims 5 to 12. as hereinbefore
13. substantially as Examples. A process according to any one of Claims 1 to 4, substantially described and with reference to the accompanying Examples. A composite structure according to any one of Claims 5 to hereinbefore described and with reference to the accompanying DATED this 17TH day of August, 1999 VIRGINIA TECH INTELLECTUAL PROPERTIES, INC. By their Patent Attorney CALLINAN LAWRIE b- Vj y, 17/08/99,a19178.c12,12
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| AU19093/97A AU715162B2 (en) | 1992-02-21 | 1997-04-24 | Recyclable molded high modulus fiber reinforced thermoplastic structures and process for preparing the same |
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| AU20140/92 | 1992-02-21 | ||
| AU20140/92A AU2014092A (en) | 1992-02-21 | 1992-02-21 | Recyclable molded high modulus fiber reinforced thermoplastic structures and process for preparing the same |
| AU19093/97A AU715162B2 (en) | 1992-02-21 | 1997-04-24 | Recyclable molded high modulus fiber reinforced thermoplastic structures and process for preparing the same |
Related Parent Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| AU20140/92A Division AU2014092A (en) | 1992-02-21 | 1992-02-21 | Recyclable molded high modulus fiber reinforced thermoplastic structures and process for preparing the same |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| AU1909397A AU1909397A (en) | 1997-08-14 |
| AU715162B2 true AU715162B2 (en) | 2000-01-20 |
Family
ID=3709497
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| AU19093/97A Ceased AU715162B2 (en) | 1992-02-21 | 1997-04-24 | Recyclable molded high modulus fiber reinforced thermoplastic structures and process for preparing the same |
Country Status (1)
| Country | Link |
|---|---|
| AU (1) | AU715162B2 (en) |
Citations (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0372740A2 (en) * | 1988-12-02 | 1990-06-13 | Ppg Industries, Inc. | Process for coating plastic substrates with powder coating compositions |
-
1997
- 1997-04-24 AU AU19093/97A patent/AU715162B2/en not_active Ceased
Patent Citations (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0372740A2 (en) * | 1988-12-02 | 1990-06-13 | Ppg Industries, Inc. | Process for coating plastic substrates with powder coating compositions |
Also Published As
| Publication number | Publication date |
|---|---|
| AU1909397A (en) | 1997-08-14 |
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