The present invention relates generally to fiber-reinforced materials and more specifically to a conformable surfacing veil or reinforcement mat.
Surfacing veils are used extensively in the reinforced plastics industry to provide improved appearance and corrosion resistance. These veils essentially act as sponges that support a resin-rich layer at the surface of the reinforced plastic article. Surfacing veils help prevent print-through of contours of the bundles of reinforcing fibers that lay beneath the surface.
Most commonly used surfacing veils consist of either glass or polyester fibers. Glass surfacing veils are usually produced by either a dry-laid or wet-laid process and typically employ a resin binder to hold the fibers together. Polyester surfacing veils are generally formed using a spun bonded or woven construction process.
Glass surfacing veils are generally less costly than polyester surfacing veils and typically offer better compatibility with a wide variety of resins because the glass fibers have a higher surface energy that allows them to be more easily wet out within the matrix resin.
The principal disadvantage of glass surfacing veils is that they have difficulty conforming to complex shapes. The glass fibers themselves do not elongate significantly under stress and have much higher bending stiffness compared to polyester fibers. Thus, if a glass-surfacing veil is placed in a recessed region with compound curvature, the glass veil will likely form a crease. Further, if glass veils are placed over a protruding region such as a boss, the lack of elongation will likely cause the surfacing veil to tear.
It is therefore highly desirable to introduce a new surfacing veil that combines most of the positive attributes of glass-fiber and polyester-fiber surfacing veils without the associated deficiencies.
It is a further object of the present invention to create plastic articles having the new surfacing veil that offers desired surface appearance and desired reinforcing properties.
A conformable surfacing veil having an improved soft feel is formed by admixing a thermoplastic sheath-core bicomponent fiber with a structural fiber to form a core composition for the mat.
The bicomponent fiber is formed from a core material and a sheath material. Suitable core materials include thermoplastic polymers such as polyethylene terephthalate (PET) that have a higher melting point than the sheath material. Suitable sheath materials include polyethylene, polypropylene, and copolyesters having softening points lower than PET. Thus, when the mixture of glass fibers and bicomponent fibers is heated above the softening point of the sheath materials, the bicomponent fiber will fuse to the glass fibers. The non-woven structures produced are tough and stretchy and have a much softer feel than standard glass veils.
In an alternative preferred embodiment, a plurality of crimped fibers, some or all of which may be hollow, can replace a portion of the wet use chop strands in the veil. The crimped fibers increase the loft of the nonwoven structure, providing a thicker reinforcing layer without increasing the weight of the surfacing veil.
In another alternative preferred embodiment, a plurality of spiral or randomly coiled fibers may replace some or all of the wet use chop strands in the veil. Similar to the crimped fibers, these coiled fibers add loft to the veil, therein forming a lighter veil per unit volume without degrading strength characteristics.
In another alternative preferred embodiment, a plurality of polymeric expandable microspheres may be added to the conformable veil. These microspheres expand when heated, and thus provide additional loft to the conformable veil.
The conformable veils of the present invention may be introduced into the reinforced plastic article independently of the primary reinforcements. Alternatively, the conformable veils may be combined with other reinforcing mats or fabrics by stitching or heat laminating.
Other objects and advantages of the present invention will become apparent upon considering the following detailed description and appended claims, and upon reference to the accompanying drawings.
The present invention is directed to a improved surfacing veil for use extensively in the reinforced plastics industry. The surfacing veils support the resin-rich surface layer of the reinforced plastic articles to improve surface appearance and improve corrosion resistance. The surfacing veils of the present invention can be produced using either a wet-laid or dry-laid process and is described below.
Referring now to
As best shown in
The bi-component fibers 24 have linear densities in the range of about 1 to 10 denier (corresponding to a fiber diameter of approximately 10 to 35 microns) and more preferably about 2 to 4 denier (approximately 15 to 20 microns). Length of the bi-component fibers 24 may range from less than about 0.25 inch to 3 inches and longer.
It should be understood that the melting/bonding temperatures recited directly above will be inherent features of the particular sheath and core polymers chosen. Accordingly, they may vary greatly from the temperatures given. What is important is that there be a significant difference between the melting point of the core 26 and the melting temperature of the sheath 28 and furthermore that the melting temperature of the sheath 28 be the lower of the two values. So configured, the sheath 28 will melt/bond at a lower temperature than the core 26, the features and benefits thereof within the context of the present invention being more fully described subsequently.
The structural fibers 22 preferably consist of high strength fibrous materials compatible with the plastics within which they are used. Two preferred structural fibers include glass fibers and polyester fibers. One preferred structural fiber 22 consists of Owens Corning's Advantex® glass fibers in the form of wet-used chopped strands. However, other preferred glass fibers that may be utilized include other E-type glass filaments, S-type glass filaments, alkaline resistant glass filaments, C-glass filaments or ECR-type glass filaments. Preferably, the glass fibers will have a diameter of 6 to 25 microns, and more preferably 10 to 23 microns. The length of the fibers may vary from less than 0.125 inch to more than 3 inches.
Preferred polyester fibers include straight, round, cut staple filaments of poly(ethylene terephthalate) such as Type 100 polyester staple manufactured and sold by KoSa. Other preferred polyester fibers include staple fibers with hollow, trilobal, or pentalobal cross-sections. These preferred fibers may have a linear density of less than 0.5 denier to more than 15 denier, and more preferably 1.5 denier to 6 denier. The length of the fibers may vary from less than 0.25 inch to more than 3 inches.
Other preferred structural fibers include carbon fibers and metal fibers. These fibers are electrically conductive and when introduced near the surface of a plastic article as part of the surfacing veil will increase the surface conductivity of the part. An electrically conductive surface facilitates the painting of the plastic article by electrostatic techniques.
In alternative preferred embodiments, as shown in
As shown in
As shown in
In another alternative preferred embodiment, as shown in
While not shown if
The whitewater chemical dispersion 52 is used to obtain reasonable filamentation of structural fibers 22 and the bicomponent fibers 24 through steric, thermodynamic, and charge colloidal interactions. The preferred whitewater dispersion 52 includes a viscosity modifier, a defoamer and a surfactant.
The viscosity modifiers used in the whitewater dispersion 52 are commonly used in nonwoven-type applications. One preferred class of viscosity modifiers is a polyacrylamide viscosity modifier such as Nalco 7768, Magnifloc 1886A, and HyChem AE 874. Another preferred viscosity modifier is a hydroxyethylcellulose, such as Natrosol 250HHBR. However, other possible viscosity modifiers or flocculants that may be used include high molecular weight, water-soluble polymers that are well known to those of ordinary skill in the art.
The surfactants, or cationic dispersants, used in the whitewater dispersion 52 aid in the wetting of the structural fibers 22 and bicomponent fibers 24 so that bundles of the fibers 22, 24 will disperse into individual filaments. One class of surfactants utilized are ethoxylated alkylamine dispersants such as Schercopol DS-140, Nalco 8493, or Rhodameen VP532. However, other dispersants may be used as well, including fatty acid amine oxides and polyethoxylated derivatives of amide condensation of fatty acid products.
Also, preferred defoamers utilized in the whitewater dispersion 52 include Nalco PP04-3840 and GEO FM LTX.
The thick slurry 54 is then delivered through a control valve 58 and combined with a whitewater stream 76 from a silo 78 to form a lower consistency slurry 80 in the former 82. The ratio of thick slurry 54 to the silo stream 78 in the lower consistency slurry 80 will typically be in the range of 1:10 and 1:40.
The former 82, or headbox, functions to equally distribute and randomly align the fibers 22, 24 onto a moving woven fabric, or forming wire 96, therein forming the filament network 14. Formers 82 that can accommodate the initial fiber formation include Fourdrinier machines, Stevens Former, Roto Former, Inver Former, cylinder, and VertiFormer machines. These formers offer several control mechanisms to control fiber orientation within the network 14 such as drop leg and various pond regulator/wall adjustments.
Deposited fibers forming the network 14 are partially dried over a suction box 94. The dewatered network 14 is then run through a drying oven 97 at a temperature sufficient to remove any excess water and sufficient to melt the sheath 28 without melting the core 26 of the bicomponent fiber, typically about 150-200 degrees Celsius. Upon removal from the oven 97, the sheath 28 material cools and adheres to both the core 26 and to the structural fibers 22, therein forming a conformable surfacing veil 20. The conformable veil 20 formed herein produces a tough, stretchy product with a much softer feel than standard glass surfacing veils.
While a wet laid process as described above is one preferred process for forming the conformable veil 20 because of its greater weight uniformity and fast production rate (up to about 1200 feet per minute), a wet laid process is best suited for use with shorter fibers to form light, thin nonwoven mats.
To form heavier mats having a basis weight of greater than 300 grams per square meter, a dry laid process is preferred. Dry laid processes can be used to create loftier veils (and mats) formed from longer fibers, but utilize slower line speeds (about 50-200 feet per minute maximum). One preferred dry-laid process, as shown in
Referring now to
While not shown, the bonding area 114 processes the filament network 14 in a manner similar to oven 97 in
One feature of the conformable veil 20 is that upon reheating of the veil 20, the sheath 28 of the bicomponent fiber 24 will again soften. This allows the conformable veil 20 to be thermally laminated to other materials. For example, stitched multilayer or multi-axial fabrics are commonly used as a reinforcement in plastic articles, such as boat hulls, manufactured by a vacuum infusion process. Generally, surfacing veils cannot be stitched to the reinforcing fabric because the depressions created by the stitch would print-through to the surface of the part. By laying the conformable veil 20 onto a reinforcing fabric and applying heat and light pressure, the veil 20 will bond to the fabric to yield a single structure. This avoids the need to lay the surfacing veil into the mold separately from the reinforcing fabric, reducing the chance for the formation of wrinkles or voids in the molded part.
In a preferred embodiment, a veil with a basis weight of 50 g/m2 was prepared on wet process machine by mixing 540 pounds of 13 micron×18 mm Owens Corning 9501 wet chop glass fibers and 220 pounds of 3.3 dtex×12 mm KoSa Type 105 bicomponent fibers in 20000 gallons of whitewater. The slurry was mixed with vigorous agitation for approximately 10 minutes and was then transferred to the machine chest. A 1000 gallon per minute stream of this thick stock slurry was delivered into a 20000-gallon per minute white water flow and the resulting thin stock was delivered to the headbox of a Sandy Hill inclined-wire Fourdrinier machine, operating at a line speed of 350 feet per minute. The dewatered sheet is then run through a drying oven at 170 degrees Celsius without the addition of any other binder, thereby producing a tough, stretchy product with a must softer feel than standard glass veils.
In another preferred embodiment, veil with a basis weight of 200 g/m2 was prepared on the same machine as in Example 1 by mixing 1625 pounds of Owens Corning 9501 glass fibers (23 micron×37 mm) and 160 pounds of KoSa Type 105 bicomponent fibers (3.3 dtex×12 mm) in 20,000 gallons of whitewater. In a manner similar to Example 1, this thick stock slurry was used to form a nonwoven web at a line speed of 250 feet per minute. This mat was dewatered and dried at a temperature of 170 degrees Celsius. The mat formed here is much more flexible and has a much softer feel than Owens Corning VL8101 reinforcement mat, which is comprised of the same glass fibers but bonded with an amount of thermosetting acrylic binder, equivalent to the amount of bicomponent fiber in the present example.
Potential applications for the conformable veil 20 formed in accordance with the present invention include a surfacing veil for the molding of reinforced plastic articles with compound curvature such as cafeteria trays; a surfacing veil for the pultrusion of thin-walled parts with complex shapes such as window lineals; a surfacing veil that can be thermally laminated to a multi-axial reinforcing fabric used in vacuum-infusion molding of boat hulls and rotor blades of wind energy turbines; and as the core of a multi-axial reinforcing fabric for vacuum infusion molding where the use of crimped fibers for loft and recovery will provide an enhanced flow medium for the infused resin.
Prior to its incorporation into the reinforced plastic articles, the conformable veil 20 may also be printed with designs, logos, or text. These designs may be directly printed onto the veil by a technique such as offset lithography or by transfer printing using a technique such as dye-sublimation. When incorporated into a reinforced plastic article using a clear or translucent matrix resin or a clear gel coat, a printed conformable surfacing veil allows the introduction of a design, logo, or text that is integral to the article and eliminates the need to apply such designs by painting or affixing a label to the article.
While the invention has been described in terms of preferred embodiments, it will be understood, of course, that the invention is not limited thereto since modifications may be made by those skilled in the art, particularly in light of the foregoing teachings.