Composite Railroad Tie and Method of Manufacturing Same
20170113423 ยท 2017-04-27
Inventors
- Joshua Lynn McCroskey (Bluff City, TN, US)
- Brian Christopher Lancaster (Bristol, TN, US)
- Bill Joe Harlow (Bristol, TN, US)
- David Edward Gibbs (Bristol, VA, US)
Cpc classification
B29C48/304
PERFORMING OPERATIONS; TRANSPORTING
B29K2031/00
PERFORMING OPERATIONS; TRANSPORTING
B29K2995/0012
PERFORMING OPERATIONS; TRANSPORTING
B29C48/09
PERFORMING OPERATIONS; TRANSPORTING
C08J9/32
CHEMISTRY; METALLURGY
B29C70/66
PERFORMING OPERATIONS; TRANSPORTING
B29C70/523
PERFORMING OPERATIONS; TRANSPORTING
B29C48/16
PERFORMING OPERATIONS; TRANSPORTING
B29C48/32
PERFORMING OPERATIONS; TRANSPORTING
B29K2105/12
PERFORMING OPERATIONS; TRANSPORTING
International classification
B29C70/52
PERFORMING OPERATIONS; TRANSPORTING
C08J9/18
CHEMISTRY; METALLURGY
Abstract
Lightweight composite structural articles having a shell and core comprising a specially-formulated resin, and methods of manufacturing the same. In particular embodiments, the present invention relates to a composite railroad tie comprising an outer fiber-reinforced polymer shell and a unique core formed from a thermoexpandable resin mixture with microcapsules, which railroad tie is manufactured by extruding or pultruding the shell and core through a specially adapted die having a graded cavity, allowing for controlled expansion of the core as the shell and core are passed through the die.
Claims
1. A method of manufacturing a composite structural form, the method comprising: providing a shell comprising a first resin composition; disposing a second resin composition with a different composition than the first resin composition in a cavity of the shell to provide a core; and passing the shell and the core through a die to prepare a composite structural form.
2. The method of claim 1, wherein the first resin composition and the second resin composition are pultruded through a die to prepare a composite structural form.
3. The method of claim 1, wherein the first resin composition and the second resin composition are extruded through a die to prepare a composite structural form.
4. The method of claim 1, wherein the first resin composition and the second resin composition are continuously passed through a die to prepare a composite structural form.
5. The method of claim 1, wherein the cavity is defined by an elongated channel in the shell.
6. The method of claim 1, wherein the shell is disposed in the die with the elongated channel oriented in a direction capable of receiving the second resin during the passing of the shell through the die.
7. The method of claim 1, wherein the shell is three-sided and provides an elongated opening in the shell.
8. The method of claim 1, wherein the shell comprises a tubular shape.
9. The method of claim 1, wherein the second resin composition is allowed to fuse with the first resin composition as the first and second resin compositions are subjected to conditions capable of curing the first and second resin compositions.
10. The method of claim 1, wherein the first resin composition and the second resin composition are subjected to conditions capable of curing the first and second resin compositions.
11. A composite structure comprising: a shell comprising a first resin composition; and a core having a second resin composition comprising: thermosetting resin; a catalyst matrix; reinforcement material; and expandable microcapsules.
12. The composite structure of claim 11, wherein the shell provides an elongated channel in the shell.
13. The composite structure of claim 11, wherein the shell is three-sided and provides an elongated channel in the shell.
14. The composite structure of claim 11, wherein the shell comprises a tubular shape.
15. The composite structure of claim 11, wherein the article is a railroad tie.
16. The composite structure of claim 11, wherein the shell comprises a base and two side walls and the two side walls are parallel to one another.
17. The composite structure of claim 11, wherein the shell comprises a base and only two side walls, wherein the two side walls are parallel to one another and wherein each side wall is disposed perpendicular to the base.
18. A resin composition comprising: a) thermosetting resin; b) a catalyst matrix; c) reinforcement material; and d) expandable microcapsules.
19. The resin composition of claim 18, wherein the expandable microcapsules are thermally expandable microcapsules comprising a polymer shell encapsulating a gas blowing agent.
20. The resin composition of claim 18 comprised of about 50 to 90 weight percent of the thermosetting resin, from about 0.2 to 10 weight percent of the catalyst matrix, from about 15 to 50 weight percent of the reinforcement material, and from about 0.5 to 30 weight percent of the expandable microcapsules based on total weight of the resin composition.
21. The resin composition of claim 18, which is cured and is in the shape of a railroad tie.
22. An article of manufacture comprising a forming die with an interior having a graded change in volume such that the volume of the interior changes from a first section of the die to a second section of the die.
23. A forming die comprising: a housing; an inlet disposed at a proximal end of the housing; a shaping cavity in communication with the inlet and terminating at a distal end of the housing; an outlet disposed at the distal end of the housing and in communication with the shaping cavity; wherein the shaping cavity is configured to provide for a first smaller cross-sectional area at the proximal end of the housing and a second larger cross-sectional area at the distal end of the housing.
24. The forming die of claim 23, wherein the inlet and the outlet each have an opening with an area and the area of the opening of the inlet is 20-45% of the area of the opening of the outlet.
25. The forming die of claim 23, wherein the inlet is a U-shaped inlet and the outlet is square or rectangular.
26. The forming die of claim 23, wherein the shaping cavity is defined by a die floor and a die ceiling and the die ceiling is sloped upwardly relative to the die floor at an angle ranging from 20-50% between the first smaller cross-sectional area and the second larger cross-sectional area.
Description
BRIEF DESCRIPTION OF THE DRAWINGS
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DETAILED DESCRIPTION OF VARIOUS EMBODIMENTS OF THE INVENTION
[0086] Reference will now be made in detail to various exemplary embodiments of the invention. However, the embodiments described in the description and shown in the figures are illustrative only and are not intended to limit the scope of the invention, and changes may be made in the specific embodiments described in this specification and accompanying drawings that a person of ordinary skill in the art will recognize are within the scope and spirit of the invention. The claims include representative embodiments as well.
[0087] In one embodiment, a composite structure is created using pultrusion of an FRP shell and a lower-density, reinforced thermoset core resin. For example, an FRP shell is created by pulling reinforcements into a resin impregnation bath. Those resin saturated reinforcements are formed into an open-shaped three-sided shell. (Open-shaped is a term of art that means a shape whereby at least one of the shape's segments, sides, or edges is not connected to anything at one of its endpoints, such that the shape is not a closed figure.) The shell is pulled into a curing die and the core resin composition is introduced into the cavity of the shell. The core resin expands to take the shape of the cavity and fill the cavity up to or near the upper edge of the open-shaped shell, thereby forming a rectangular, elongated structure suitable for using as a railroad tie. As heat is applied to the die, the fiber-reinforced polymer shell and the core resin harden. Similarly, if a tubular shell is preferred, core resin may be introduced at an opening in the front or back end of the tube as the tube is being pultruded into the die. Alternatively, the shell can be wrapped around the core resin as the shell and core resin are pultruded through the die. In yet another embodiment, the core resin could be extruded, or pushed, into the tubular structure as the tubular structure is being pulled into the die.
[0088] In one preferred embodiment, the FRP shell and the core resin are cured at the same time. During this preferred process, a portion of the FRP shell will bleed into the core resin where the core resin meets the FRP shell. As the FRP shell and the core resin harden together as they are heated, this intermingling of the FRP shell resin and the core resin creates a fusion of the FRP shell resin and the core resin around the areas where the FRP shell resin and the core resin meet and interact, thereby strengthening the bond of the FRP shell resin to the core resin. This process occurs in a continuous pultrusion process. Continuous bears the meaning one of ordinary skill in the art would give to such a term as used in the context of a pultrusion or extrusion, which is effectively that the process is performed in a sequence.
[0089] In a similar manner, this process can be performed by an extrusion method. In a preferred method, a molten resin would be pushed through a die, thereby forming a three-sided shell structure. The resulting structure would be cooled and the core resin would be deposited into the cavity of the three-sided structure. The core resin would be heated as the composite structure of the shell and core pass through a die. In another preferred method, the core resin composition without any shell could be extruded (or pultruded) through a die and cured to form a structure suitable to use as, for example, a railroad tie.
[0090] A preferred shape of the interior of the die used to make the structural article includes a gradient whereby the volume of the interior of the die is increased in a graded manner from a point when the core resin is injected into the cavity to a point where the FRP shell and core resin exit the die. Consequently, when the core resin is inserted into the core of the FRP shell, the die allows it to expand over time until it fills the FRP shell. The core resin preferably moves through the die at a rate that allows for the resin to expand to fill the cavity. Such a die and the corresponding process will result in a varying cross section of the structural article (e.g., railroad tie) over time. Thus, in embodiments, a cross section of the structure viewed at one time during formation will not be identical to a cross section viewed at another time during formation. This is unique in that a pultruded product, for example, is historically made with a continuous cross section that will look identical or substantially identical regardless of when a cross section of the structure during formation is viewed over time, unlike a preferred embodiment of the present invention where the cross section will not be identical when viewed at different times during the formation process.
[0091] In a preferred embodiment of the product resulting from the described manufacturing process, a structure is formed, which may act as a railroad tie, the core of which structure comprises the following ingredients: thermosetting resin, catalyst matrix, reinforcement materials, and expandable microcapsules. The shell of such a preferred embodiment is preferably a U-shaped or three-sided FRP structure with a density equal to or greater than the core. Such a shell is preferably an open-shaped structure whereby one side of the elongated structure in the axial direction is open, and whereby the ends of the elongated structure are open, but the ends may be capped.
[0092] In embodiments, especially for railroad tie embodiments, the finished structure is approximately 9 inches wide and about 7 inches tall and can be any length, such as about 2 feet, 3 feet, 4 feet, 5 feet, 6 feet, 7 feet, 8 feet, 9 feet, 10 feet, 11 feet, 12 feet, 13 feet, 14 feet, 15 feet, 16 feet, 17 feet, 18 feet, 19 feet, or 20 feet and so on. A preferred length is one for which the structure can be used as a railroad tie. The structure can be any width and any height. Some exemplary widths include from about 1 inch to about 60 inches, such as from about 1 inch to about 2 inches, from about 2 inches to about 3 inches, from about 3 inches to about 4 inches, from about 4 inches to about 5 inches, from about 5 inches to about 6 inches, from about 6 inches to about 7 inches, from about 7 inches to about 8 inches, from about 8 inches to about 9 inches, from about 9 inches to about 10 inches and so on. Likewise, the structure can be any height and exemplary heights can include from about 1 inch to about 24 inches, by way of example only. Indeed, any combination of thickness, width or length can be used for the claimed structures, especially one or more of the parameters specified in this specification.
[0093] In embodiments, the finished structure weighs approximately 10% to 75% less than a standard railroad tie made of wood, such as about 10% to 20% less, about 20% to 30% less, about 30% to 40% less, about 40% to 50% less, about 50% to 60% less, about 60% to 70% less, or about 70% to 75% less. In embodiments, the finished structure may last 4-5 times longer than a standard wood railroad tie, by way of example.
[0094] Suitable thermosetting resins for use as the FRP shell include polyester resin, vinyl ester resin, epoxy resin, phenolic resin, and urethane resin. In a preferred embodiment, the resin is an isophthalic polyester or a vinyl ester resin. During pultrusion, for example, the resin may be provided in a mixture that includes one or more catalysts and/or accelerators. Catalysts that may be included in the resin mixture include latent catalysts that have little or no catalytic activity below a certain temperature, above which the catalyst is active. Examples of latent catalysts include phenyl hydrogen maleate, phenyl trifluoroacetate and butadiene sulfone. Other types of catalysts that may be used include acid catalysts, basic catalysts, and peroxide catalysts. Typical acid catalysts are sulfuric acid, sulfonic acids such as phenolsulfonic acid, oxalic acid, boron trifluoride, boric anhydride, boric acid and mixtures of boric acid or boric anhydride with epoxies. Typical basic catalysts include organic amines such as hexamethylenetetramine, trimethylamine, ethanolamines and oxides and hydroxides of metals such as barium, calcium, sodium and potassium. An accelerator may be included to speed up the cure rate of the resin. Typical accelerators are zinc or cobalt salts.
[0095] Suitable reinforcement materials for use as the FRP shell include fiberglass, fiberglass-based material, wood-based materials, or recycled fiber-reinforced polymer. Other reinforcement materials suitable for the shell include carbon, hemp, glass, steel, twine, or anything generally that can be put into tension.
[0096] Particular examples of possible ingredients for a suitable catalyst mixture for the FRP shell include Perkadox 16 (a di(4-tert-butylcyclohexyl) peroxydicarbonate) (www.akzonobel.com/polymer/our_products/perkadox_16-40ps/), Trigonox 121-C75 (a tert-Amylperoxy-2-ethylhexanoate) (www.akzonobel.com/fc/brands_products/product_search/product_finder_detail.aspx?id=12426), Tringonox EHPTS (a Di(2-ethylexyl) peroxydicarbonate, stabilized) (akzonobel.com/polymer), Trigonox 121-BB75 (a tert-Amyl-peroxy-2-ethylhexanoate), and Trigonox C (a tert-Butyl peroxybenzoate).
[0097] Particular examples of suitable resin for the FRP shell include resin supplied by Ashland Performance, such as Polyester 2036 Modified, and as supplied by AOC Solutions, such as P706-500. Particular examples of mats and rovings to reinforce the FRP shell include MatVantage II (a continuous filament mat without binder) and various rovings supplied by PPG, as well as M8643 and equivalents (continuous filament mats with binders) and various rovings supplied by Owens Corning. Some recycled mat and rovings may also be used in the core resin composition. A particular example of filler includes ASP400P supplied by Superior Materials, Inc. A particular example of a veil to, for example, provide a surface protectant from UV light and corrosive environments, includes the veil supplied by Xamax. A particular example of Styrene which may be used in the FRP shell is supplied by Chemsolv. A particular example of a release which may be used in the FRP shell includes SR150 supplied by Technick Products. A particular example of additives BHT which may be used in the FRP shell to inhibit the catalyst and thereby prevent premature curing in the resin bath is supplied by Composites One. Particular examples of fire retardants which may be used in the shell include bromine, antimony, and ATH (alumina trihydrate), such as those supplied by Azalea Color/Omya Distribution.
[0098] A preferred density value for the shell is around 0.07 lbs/in.sup.3. The density value for the shell may be about 0.01 lbs/in.sup.3 to 5 lbs/in.sup.3, such as about 0.01 lbs/in.sup.3 to 0.05 lbs/in.sup.3, about 0.05 lbs/in.sup.3 to 0.1 lbs/in.sup.3, about 0.1 lbs/in.sup.3 to 0.15 lbs/in.sup.3, about 0.15 lbs/in.sup.3 to 0.20 lbs/in.sup.3, about 0.2 lbs/in.sup.3 to 0.25 lbs/in.sup.3, about 0.25 lbs/in.sup.3 to 0.3 lbs/in.sup.3, about 0.3 lbs/in.sup.3 to 0.35 lbs/in.sup.3, about 0.35 lbs/in.sup.3 to 0.4 lbs/in.sup.3, about 0.4 lbs/in.sup.3 to 0.45 lbs/in.sup.3, about 0.45 lbs/in.sup.3 to 0.5 lbs/in.sup.3, and so on. A preferred tensile strength for the shell is around 2.510.sup.6 psi. The tensile strength of the shell may be about 0.510.sup.6 psi to 5.010.sup.6 psi, such as about 0.510.sup.6 psi to 110.sup.6 psi, about 110.sup.6 psi to 1.510.sup.6 psi, about 1.510.sup.6 psi to 210.sup.6 psi, about 210.sup.6 psi to 2.510.sup.6 psi, about 2.510.sup.6 psi to 310.sup.6 psi, and so on.
[0099] Suitable thermosetting resins for use as the matrix of the core resin composite include polyester resin, vinyl ester resin, epoxy resin, phenolic resin, and urethane resin. In a preferred embodiment, the resin is an isophthalic polyester or a vinyl ester resin. During pultrusion, the resin may be provided in a mixture that includes one or more catalysts and/or accelerators. Catalysts that may be included in the resin mixture include latent catalysts that have little or no catalytic activity below a certain temperature, above which the catalyst is active. Examples of latent catalysts include phenyl hydrogen maleate, phenyl trifluoroacetate and butadiene sulfone. Other types of catalysts that may be used include acid catalysts, basic catalysts, and peroxide catalysts. Typical acid catalysts are sulfuric acid, sulfonic acids such as phenolsulfonic acid, oxalic acid, boron trifluoride, boric anhydride, boric acid and mixtures of boric acid or boric anhydride with epoxies. Typical basic catalysts include organic amines such as hexamethylenetetramine, trimethylamine, ethanolamines and oxides and hydroxides of metals such as barium, calcium, sodium and potassium. An accelerator may be included to speed up the cure rate of the resin. Typical accelerators are zinc or cobalt salts.
[0100] Particular examples of suitable resin for the core resin include resin supplied by Ashland Performance, such as Polyester 2036 Modified, and as supplied by AOC Solutions, such as P706-500. Preferable boiling points for resin in the core resin include boiling points between 100 and 400 degrees Fahrenheit, such as about 100 degrees F. to 120 degrees F., about 120 degrees F. to 140 degrees F., about 140 degrees F. to 160 degrees F., about 160 degrees F. to 180 degrees F., about 180 degrees F. to 200 degrees F., about 200 degrees F. to 220 degrees F., about 220 degrees F. to 240 degrees F., about 240 degrees F. to 260 degrees F., about 260 degrees F. to 280 degrees F., about 280 degrees F. to 300 degrees F., about 300 degrees F. to 320 degrees F., about 320 degrees F. to 340 degrees F., about 340 degrees F. to 360 degrees F., about 360 degrees F. to 380 degrees F., or about 380 degrees F. to 400 degrees F. The viscosity of the resins which may be used in the core resin composition may, for example, be from 1,000 to 20,000 centipose (cps), such as about 1,000 cps to 2,000 cps, about 2,000 cps to 3,000 cps, about 3,000 cps to 4,000 cps, about 4,000 cps to 5,000 cps, about 5,000 cps to 6,000 cps, about 6,000 cps to 7,000 cps, about 7,000 cps to 8,000 cps, about 8,000 cps to 9,000 cps, and so on.
[0101] Particular examples of possible ingredients for a suitable catalyst mixture for the core resin include Perkadox 16 (a di(4-tert-butylcyclohexyl) peroxydicarbonate) (www.akzonobel.com/polymer/our_products/perkadox_16-40ps/), Trigonox 121-C75 (a tert-Amyl peroxy-2-ethylhexanoate) (www.akzonobel.com/fc/brands_products/product_search/product_finder_detail.aspx?id=12426), Tringonox EHPTS (a Di(2-ethylexyl) peroxydicarbonate, stabilized) (akzonobel.com/polymer), Trigonox 121-BB75 (a tert-Amyl-peroxy-2-ethylhexanoate), and Trigonox C (a tert-Butyl peroxybenzoate). A preferred embodiment of the catalyst matrix comprises around 60.55% Trigonox 121-BB75 (a tert-Amyl-peroxy-2-ethylhexanoate), 15.6% Trigonox C (a tert-Butyl peroxybenzoate), and 23.85% Perkadox 16 (a di(4-tert-butylcyclohexyl) peroxydicarbonate).
[0102] Suitable reinforcement materials for use in the core resin mixture include fiberglass, fiberglass-based material, wood-based materials, or recycled fiber-reinforced polymer. Other reinforcement materials suitable for the core resin mixture include carbon, hemp, glass, steel, twine, or anything generally that can be put into tension. A preferred embodiment includes glass rovings and glass mat reinforcement materials in the shell, and milled fibers (e.g., ground-up glass), recycled fiber-reinforced polymer, and ground-up wood reinforcements in the core.
[0103] The core resin also includes microcapsules, such as a PMMA/acrylic microcapsules. Expandable microcapsules are used to reduce the weight of products based on thermoplastics and elastomers. Preferably, the microcapsules are thermally expandable, such as thermoplastic hollow microspheres. (Microcapsules are interchangeably referred to as microspheres by those of skill in the art.) The microcapsules as disclosed herein are hollow bodies of plastic (e.g., a copolymer, such as vinylidene chloride, acrylonitrile or methyl methacrylate) encapsulating a substance that is capable of expanding when exposed to heat (such as isobutene or isopentane). Such microcapsules are not known to be in use in any other pultrusion process application. For example, the expandable microcapsules supplied by Kureha, H-1100 and M-330, are suitable acrylic microcapsules for the core resin mixture. The Expancel 461DET lines of microcapsules, products of Expancel Nobel Industries, may also be used. These thermally expandable microcapsules comprise a polymer shell encapsulating a gas blowing agent (for example, aliphatic hydrocarbons). When heated, the gas in the shell expands increasing pressure while the thermoplastic shell softens, resulting in expansion. Upon cooling a hollow and extremely light plastic sphere remains.
[0104] Microcapsules with the trade name Expancel 092 DE may also be used. Examples of other suitable materials may include, but are not limited to, Expancel DU, Expancel MB, Expancel DE, Expancel 551DE, Expancel 091DU, Expancel 461DU, or the product names Matsumoto Microsphere F-85, Matsumoto Microsphere F-100, Microsphere FE, etc. from Matsumoto Yushi-Seiyaku of Japan, the Advancell line from Sekisui Chemical Company, Ltd., or other blowing agent microcapsules may be used without departing from the scope of the present invention.
[0105] These microcapsules can expand by a factor of at least 2, preferably 4 in diameter, resulting in a volume expansion of each particle of 64 or more. It is preferred that the microcapsules expand at the temperatures used to cure the core resin. Microcapsules may be obtained in a range of densities and it is preferred to use expandable microspheres having a density in the range of 15 Kg/m.sup.3 to 85 Kg/m.sup.3, such as about 15 Kg/m.sup.3 to 20 Kg/m.sup.3, about 20 Kg/m.sup.3 to 25 Kg/m.sup.3, about 25 Kg/m.sup.3 to 30 Kg/m.sup.3, about 30 Kg/m.sup.3 to 35 Kg/m.sup.3, about 35 Kg/m.sup.3 to 40 Kg/m.sup.3, about 40 Kg/m.sup.3 to 45 Kg/m.sup.3, about 45 Kg/m.sup.3 to 50 Kg/m.sup.3, about 50 Kg/m.sup.3 to 55 Kg/m.sup.3, about 55 Kg/m.sup.3 to 60 Kg/m.sup.3, about 60 Kg/m.sup.3 to 65 Kg/m.sup.3, about 65 Kg/m.sup.3 to 70 Kg/m.sup.3, about 70 Kg/m.sup.3 to 75 Kg/m.sup.3, about 75 Kg/m.sup.3 to 80 Kg/m.sup.3, or about 80 Kg/m.sup.3 to 85 Kg/m.sup.3. Expansion temperatures range from 80 C. to 190 C., such as about 80 C. to 90 C., about 90 C. to 100 C., about 100 C. to 120 C., about 120 C. to 140 C., about 140 C. to 160 C., about 160 C. to 180 C., or about 180 C. to 190 C. The particle size for expanded microcapsules ranges from 20-150 m, such as about 20 m to 30 m, about 30 m to 40 m, about 40 m to 50 m, about 50 m to 60 m, about 60 m to 70 m, about 70 m to 80 m, about 80 m to 90 m, about 90 m to 100 m, about 100 m to 110 m, about 110 m to 120 m, about 120 m to 130 m, about 130 m to 140 m, or about 140 m to 150 m. When fully expanded, the volume of the microcapsules can increase more than 40 times. Detailed descriptions of various expandable microcapsules and their production can be found in, for example, U.S. Pat. Nos. 3,615,972, 3,945,956, 4,287,308, 5,536,756, 6,235,800, 6,235,394, 6,509,384, 6,617,363 and 6,984,347.
[0106] A particular example of styrene which may be used in the core composition is supplied by Chemsolv. A particular example of a release which may be used in the core composition includes SR150 supplied by Technick Products. A particular example of additives BHT which may be used in the core composition to inhibit the catalyst and thereby prevent premature curing is supplied by Composites One.
[0107] An example of a preferred core mixture composition comprises about 50 to 90 weight percent total of thermosetting resin, such as about 50 to 60 weight percent total of thermosetting resin, about 60 to 70 weight percent total of thermosetting resin, about 70 to 80 weight percent total of thermosetting resin, or about 80 to 90 weight percent total of thermosetting resin. An example of a preferred core mixture composition comprises from about 0.2 to 10 weight percent total of catalyst matrix, such as about 0.2 to 1 weight percent total of catalyst matrix, about 1 to 2 weight percent total of catalyst matrix, about 2 to 3 weight percent total of catalyst matrix, about 3 to 4 weight percent total of catalyst matrix, about 4 to 5 weight percent total of catalyst matrix, about 5 to 6 weight percent total of catalyst matrix, about 6 to 7 weight percent total of catalyst matrix, about 7 to 8 weight percent total of catalyst matrix, about 8 to 9 weight percent total of catalyst matrix, or about 9 to 10 weight percent total of catalyst matrix. An example of a preferred core mixture composition comprises from about 15 to 50 weight percent total of reinforcement material, such as about 15 to 20 weight percent total of reinforcement material, about 20 to 25 weight percent total of reinforcement material, about 25 to 30 weight percent total of reinforcement material, about 30 to 35 weight percent total of reinforcement material, about 35 to 40 weight percent total of reinforcement material, about 40 to 45 weight percent total of reinforcement material, or about 45 to 50 weight percent total of reinforcement material. An example of a preferred core mixture composition comprises from about 0.5 to 30 weight percent total of microcapsules, such as about 0.5 to 5 weight percent total of microcapsules, about 5 to 10 weight percent total of microcapsules, about 10 to 15 weight percent total of microcapsules, about 15 to 20 weight percent total of microcapsules, about 20 to 25 weight percent total of microcapsules, or about 25 to 30 weight percent total of microcapsules.
[0108] In a preferred embodiment, the core resin composition comprises around 73 weight percent total of thermosetting resin, around 0.33 weight percent total of catalyst matrix, around 24 weight percent total of reinforcement material, and around 2 weight percent total of microcapsules. In another preferred embodiment, the core resin composition comprises around 72.85 weight percent total of thermosetting resin, around 0.417 weight percent total of catalyst matrix, around 28.62 weight percent total of reinforcement material, and around 2.43 weight percent total of microcapsules. In another preferred embodiment, the core resin composition comprises around 68.68 weight percent total of thermosetting resin, around 0.442 weight percent total of catalyst matrix, around 24.28 weight percent total of reinforcement material, and around 2.29 weight percent total of microcapsules.
[0109] The density of the core composition is surprisingly dense given its weight. An exemplary specimen might measure 14.8596 cubic inches and weigh 0.3210 lbs. This results in a density of 0.02160 lbs./in.sup.3. Converted to lbs./ft.sup.3, which is the unit used in, for example, Table 1 of prior art patent U.S. Pat. No. 8,342,420 (col. 6, l. 35), the density is 37.3248 lbs./ft.sup.3. By way of example, Table 1 in U.S. Pat. No. 8,342,420 teaches structures with a density ranging from 1 to 5 lbs./ft.sup.3. Therefore, the currently disclosed core composition may be approximately 7.5 times more dense than the core compositions disclosed by U.S. Pat. No. 8,342,420, yet weigh approximately the same as those taught by U.S. Pat. No. 8,342,420 (see column 5, ll. 62-65). One example of a core density to weight ratio of the currently disclosed structural articles includes a core density of 0.025 lbs./in.sup.3 and final weight of a 97102 railroad tie of 186 lbs. Another example of a core density to weight ratio of the currently disclosed structural articles includes a core density of 0.019 lbs./in.sup.3 and final weight of a 97102 railroad tie of 151 lbs. The density of the core resin could, for example, be about 0.005 lbs./in.sup.3 to 5 lbs./in.sup.3, such as about 0.005 lbs./in.sup.3 to 0.01 lbs./in.sup.3, about 0.01 lbs./in.sup.3 to 0.02 lbs./in.sup.3, about 0.02 lbs./in.sup.3 to 0.03 lbs./in.sup.3, about 0.03 lbs./in.sup.3 to 0.04 lbs./in.sup.3, about 0.04 lbs./in.sup.3 to 0.05 lbs./in.sup.3, about 0.05 lbs./in.sup.3 to 0.06 lbs./in.sup.3, about 0.06 lbs./in.sup.3 to 0.07 lbs./in.sup.3, about 0.07 lbs./in.sup.3 to 0.08 lbs./in.sup.3, and so on.
[0110] The viscosity of the core resin composition may, for example, be from 1,000 to 20,000 centipose (cps), such as about 1,000 cps to 2,000 cps, about 2,000 cps to 3,000 cps, about 3,000 cps to 4,000 cps, about 4,000 cps to 5,000 cps, about 5,000 cps to 6,000 cps, about 6,000 cps to 7,000 cps, about 7,000 cps to 8,000 cps, about 8,000 cps to 9,000 cps, and so on.
[0111] Now turning to the figures,
[0112] Alternatively, the structural article of the present invention may be made using an extrusion process.
[0113] Referring to
[0114] The resulting pre-formed reinforced shell is pulled into the die 350, and lower density core resin is introduced into the open cavity of the three-sided shell (designated by the arrows at die 350 in
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[0117]
[0118] Conventional pultrusion dies can be provided with a cavity for heat expanding resin, but are not provided with such a cavity wherein an internal sloping apparatus is used to increase the volume of the cavity over the entire length of the cavity, or a portion of the length of the cavity, so that the expanding resin rises in a controlled manner and can be done in a continuous fashion. Preferably, the end result is a rectangular shaped structure that is light but dense and can be used as a railroad tie. Accordingly, the exit of the die is preferably a rectangular shape 653.
[0119]
[0120]
[0121]
EXAMPLES
Example 1
[0122] Railroad ties of the present invention that are of significant value are those capable of passing one or more of the American Railway Engineering and Maintenance-of-Way Association Manual for Railway Engineering specifications (AREMA specifications) for Engineered Polymer Composites. (See, e.g., AREMA specifications at pp. 30-5-4 to 30-5-7 (Table 30-5-1. Physical and Mechanical Properties) (2013).)
[0123] For example, railroad ties of the present invention are preferred to meet one or more of the following physical and mechanical properties:
[0124] a. The tie shall permit the application of standard rail, tie plate, and hold-down fasteners, such as screw spikes or cut spikes, without requiring special procedures for installation other than ordinary predrilling of the tie per the manufacturer's requirements.
[0125] b. The tie shall provide an adequate flexural response to absorb train induced vibrations, while possessing sufficient vertical compressibility to withstand rail seat loading. Tie must support imposed railroad-type loadings while maintaining surface, line, and gage. Tie must transmit traffic loads to the ballast with diminished contact pressures and anchor the rail-tie structure against lateral and longitudinal movements.
[0126] c. Material surfaces shall have slip resistance equal to or better than a standard treated wood tie.
[0127] d. The tie shall not be prone to failure (e.g., cracking or fracture) due to weather-related changes in temperature.
[0128] e. The tie shall not warp or sag to the level of permanent deformation that would require replacement of the tie.
[0129] f. The tie shall not split or crack in any way requiring the tie to be replaced.
[0130] g. Material surface degradation due to solar ultraviolet (UV) radiation exposure shall not exceed 0.003 inch (0.076 mm) per year.
Example 2
[0131] The railroad ties of the present invention are preferred to meet one or more of the dimensional requirements according to the AREMA specifications; specifically:
[0132] a. All measurements performed for quality assurance purposes shall be made at 73.4+/2 F. (23+/1.1 C.) and relative humidity of 50+/5%. Alternatively, measurements may be made at ambient temperature and humidity conditions and then corrected to the specified temperature and humidity. In case of dispute, the standard conditions shall govern.
[0133] b. For a standard gage track tie, the rail-bearing areas are those sections between 20 inches (510 mm) and 40 inches (1020 mm) from the center of the tie. Tie surface flatness in the area of the tie plate shall be within 0.125 inch (3.18 mm).
[0134] c. Tie dimensions as specified shall be full size. All ties, without surface texturing, shall have a thickness tolerance+ inch (6.4 mm), 0 inch (0 mm); width tolerance+/ inch (6.4 mm); length tolerance+ inch (19 mm), 0 inch (0 mm). Ties with surface texturing shall meet nominal specified dimensions as required for the application.
[0135] d. Standard ties, 7 inch (178 mm) by 9 inch (229 mm) by 8.5 to 9 foot (2.6 m to 2.7 m) long, without surface texturing, will be considered straight when a straight line along each tie face from the middle of one end to the middle of the other end is no closer to the edge of the tie than one-half the tie face dimension, plus inch (6.4 mm) or minus inch (6.4 mm). For ties surface textured for increased track stability, this tolerance shall be a maximum plus inch (19 mm) or minus inch (19 mm).
Example 3
[0136] The railroad ties of the present invention are preferred to meet one or more Physical and Mechanical Properties according to the AREMA specifications in Table 30-5-1; specifically:
TABLE-US-00001 Polymer Test Method Composites Modulus of Elasticity Part 2, Minimum, 170,000 (in bending - center Section 2.2.3, (1,170) negative) - MOE, psi Test 1C (MPa) Modulus of Rupture Part 2, Minimum, (in bending - center Section 2.2.3, 2,000 negative) - MOR, psi Test 1C (13.8) (MPa) Rail Seat Part 2, Section 2.3, Minimum, Compression, psi Test 2 900 (MPa) (6.2) Single Tie Lateral Part 2, Section 2.9, Minimum, Push, lbf (kN), after Test 8 2,500 100,000 gross tons of (11.1) Traffic Spike/Screw Pullout, Part 2, Minimum, lbf (kN) Section 2.4.1, 1,900/5,000 Test 3A (8.5/22.2) Coefficient of ASTM D6431 Maximum, Thermal Expansion, 7.5 105 in/in/ F. (cm/cm/ C.) (1.35 10.sup.4) Electrical Impedance, Part 2, Section 2.8, Minimum, Ohms Test 7 20,000
Example 4
[0137] The railroad ties of the present invention are preferred to meet one or more Mechanical Properties according to the AREMA specifications in Table 30-A-1; specifically:
TABLE-US-00002 Dimensions (in.): Length 102 Width 9 Depth 7 Volume (ft.sup.2) 3.72 Density, pcf (lbs/ft.sup.2) 50-86 Weight (lbs) 186-320 Moment of Inertia (in.sup.4) Seat 257 Center 257 Section Modulus (in.sup.3) RS+ RS C 73.5 C+ Modulus of Elasticity (MOE) (10.sup.6 psi) 40 F. +72 F. 140 F. 0.17 Modulus of Rupture (MOR) (psi) 40 F. +72 F. 2,000 140 F. Rail Seat Compression Test (psi) 900 Material Surface Hardness Test Janka Ball 5,000 (lbs) Single Tie Lateral Push Test (lbs) 1,500-4,000+
[0138] The present invention has been described with reference to particular embodiments having various features. It will be apparent to those skilled in the art that various modifications and variations can be made in the practice of the present invention without departing from the scope or spirit of the invention. One skilled in the art will recognize that these features may be used singularly or in any combination based on the requirements and specifications of a given application or design. Embodiments comprising various features may also consist of or consist essentially of those various features. Other embodiments of the invention will be apparent to those skilled in the art from consideration of the specification and practice of the invention. The description of the invention provided is merely exemplary in nature and, thus, variations that do not depart from the essence of the invention are intended to be within the scope of the invention. All references cited in this specification are hereby incorporated by reference in their entireties.