US20070087181A1 - Variegated composites and related methods of manufacture - Google Patents

Variegated composites and related methods of manufacture Download PDF

Info

Publication number
US20070087181A1
US20070087181A1 US11/544,567 US54456706A US2007087181A1 US 20070087181 A1 US20070087181 A1 US 20070087181A1 US 54456706 A US54456706 A US 54456706A US 2007087181 A1 US2007087181 A1 US 2007087181A1
Authority
US
United States
Prior art keywords
polymer
composite
color
wood fibers
amorphous
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Abandoned
Application number
US11/544,567
Inventor
Blair Dolinar
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Trex Co Inc
Original Assignee
Trex Co Inc
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 Trex Co Inc filed Critical Trex Co Inc
Priority to US11/544,567 priority Critical patent/US20070087181A1/en
Publication of US20070087181A1 publication Critical patent/US20070087181A1/en
Assigned to BRANCH BANKING AND TRUST COMPANY, AS COLLATERAL AGENT reassignment BRANCH BANKING AND TRUST COMPANY, AS COLLATERAL AGENT SECURITY AGREEMENT Assignors: TREX COMPANY, INC.
Abandoned legal-status Critical Current

Links

Images

Classifications

    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L97/00Compositions of lignin-containing materials
    • C08L97/02Lignocellulosic material, e.g. wood, straw or bagasse
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10TTECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T428/00Stock material or miscellaneous articles
    • Y10T428/249921Web or sheet containing structurally defined element or component
    • Y10T428/249924Noninterengaged fiber-containing paper-free web or sheet which is not of specified porosity
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10TTECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T428/00Stock material or miscellaneous articles
    • Y10T428/249921Web or sheet containing structurally defined element or component
    • Y10T428/249924Noninterengaged fiber-containing paper-free web or sheet which is not of specified porosity
    • Y10T428/249925Fiber-containing wood product [e.g., hardboard, lumber, or wood board, etc.]
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10TTECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T428/00Stock material or miscellaneous articles
    • Y10T428/25Web or sheet containing structurally defined element or component and including a second component containing structurally defined particles
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10TTECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T428/00Stock material or miscellaneous articles
    • Y10T428/25Web or sheet containing structurally defined element or component and including a second component containing structurally defined particles
    • Y10T428/254Polymeric or resinous material
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10TTECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T428/00Stock material or miscellaneous articles
    • Y10T428/31504Composite [nonstructural laminate]
    • Y10T428/31971Of carbohydrate
    • Y10T428/31989Of wood

Definitions

  • the invention is directed to variegated wood-plastic composites and methods of manufacturing the same.
  • the surfaces of the wood-plastic composites may be variegated by varying the polymer composition of the wood-plastic composite.
  • the invention also includes a method of manufacturing the wood-plastic composites such that one polymer is shifted in the composite relative to the other polymer.
  • Wooden components are commonly used in manufacturing decks and related assemblies. Wooden components includes strings of wood fibers having various colors (e.g., rings on trees) that give the surface of the wooden component a streaked appearance. The streaked appearance imparts an aesthetically pleasing look and feel to the deck component.
  • a more environmentally friendly alternative to using wooden components in manufacturing decks and related assemblies is to use a wood-plastic composite made of crystalline polymers.
  • suitable wood-plastic composites made of crystalline polymers and related methods of manufacture are disclosed in co-owned U.S. Pat. Nos. 5,851,469 and 6,527,532, co-pending and co-owned U.S. patent application Ser. No. 10/292,672 filed Nov. 12, 2002, and co-pending and co-owned U.S. patent application Ser. No. 10/668,368 filed Sep. 24, 2003, the entirety of all of which are incorporated herein by reference.
  • Wood-plastic composites made of crystalline polymers tend to have solid one color surfaces. This is at least partially due to the sharp melting point temperatures of crystalline polymers and the tendency of crystalline polymers to easily blend together. Thus, even if a plurality of crystalline polymers having a plurality of different colors are used to manufacture a wood-plastic composites, the plurality of different colors will blend together in the manufacturing process and the composite will emerge having a surface with one solid color. In any case, the resultant composite does not have a streaked appearance.
  • An exemplary embodiment of the invention includes a composite.
  • the composite comprises a crystalline polymer, a plurality of wood fibers blended with the crystalline polymer, an outer surface, and an amorphous polymer visible on the outer surface.
  • the amorphous polymer has a first color and the blend of the crystalline polymer and the plurality of wood fibers has a second color different from the first color.
  • the invention may include one or more of the following aspects: the crystalline polymer may be at least one of polypropylene and polyethylene; the amorphous polymer may be a styrenic polymer; the outer surface may include streaks of the first color; the amorphous polymer may have a melting temperature that is substantially the same as a melting temperature of the crystalline polymer; the outer surface may be variegated; a first portion of the outer surface may have the first color and a second portion of the outer surface may have the second color; another amorphous polymer visible on the outer surface; the another amorphous polymer may have a third color different from the first color and the second color; the composite may be at least one of a building material, a decking material, and a decking board; a colorant may be blended with one of the crystalline polymer and the amorphous polymer.
  • the composite may include a first polymer, a plurality of wood fibers blended with the first polymer, an outer surface, and a second polymer configured to resist blending with the first polymer.
  • the composite may be manufactured such that the second polymer is deliberately visible on the outer surface.
  • the blend of the first polymer and the plurality of wood fibers may have a first color and the second polymer may have a second color different from the first color.
  • the second polymer may not be substantially soluble in the first polymer.
  • the invention may include one or more of the following aspects: the first polymer may be at least one of polypropylene and polyethylene; the second polymer may be a styrenic polymer; the outer surface may include streaks of the second color; the first polymer may have a melting temperature that is substantially the same as a melting temperature of the second polymer; the outer surface may be variegated; a first portion of the outer surface may have the first color and a second portion of the outer surface has the second color; a third polymer may be configured to resist blending with the first polymer; the composite may be manufactured such that the third polymer is deliberately visible on the outer surface; the third polymer may have a third color different from the first color and the second color; the composite may be at least one of a building material, a decking material, and a decking board; a colorant blended with one of the first polymer and the second polymer.
  • a further embodiment of the invention may include a method of manufacturing a wood-plastic composite.
  • the method may include providing a crystalline polymer, providing a plurality of wood fibers, providing an amorphous polymer, melting the crystalline polymer, melting the amorphous polymer, mixing the amorphous polymer with the crystalline polymer and the plurality of wood fibers to form a feed, and forming a profile body from the feed, the profile body including an outer surface evincing a first color and a second color different from the first color.
  • the invention may include one or more of the following aspects: forming streaks of the first color on the outer surface; forming streaks of the amorphous polymer on the outer surface; shifting the amorphous polymer towards the outer surface; variegating the outer surface; providing at least one of a single screw extruder and a double screw extruder; the step of extruding may include extruding the feed via the at least one of the single-screw extruder and the double screw extruder; the step of mixing may include forming the first color from the amorphous polymer and forming the second color from a blend of the crystalline polymer and the plurality of wood fibers; providing another amorphous polymer, melting the another amorphous polymer; mixing the another amorphous polymer with the amorphous polymer, the crystalline polymer, and the plurality of wood fibers; the step of extruding may include forming the profile body such that the outer surface evinces a third color different from the first color and
  • Yet another embodiment of the invention may include a method of manufacturing a wood-plastic composite.
  • the method may include providing a first polymer, providing a plurality of wood fibers, providing a second polymer not substantially soluble in the first polymer, melting the first polymer, melting the second polymer, mixing the second polymer with the first polymer and the plurality of wood fibers to form a feed, and forming a profile body from the feed, the profile body including an outer surface deliberately evincing a first color and a second color different from the first color.
  • the invention may include one or more of the following aspects: forming streaks of the first color on the outer surface; forming streaks of the first polymer on the outer surface; shifting the first polymer towards the outer surface; variegating the outer surface; providing at least one of a single screw extruder and a double screw extruder; the step of extruding may include extruding the feed via the at least one of the single-screw extruder and the double screw extruder; the step of mixing may include forming the first color from the first polymer and forming the second color from a blend of the second polymer and the plurality of wood fibers; providing a third polymer not substantially soluble in the first polymer; melting the third polymer; mixing the third polymer with the first polymer, the second polymer, and the plurality of wood fibers; the step of extruding may include forming the profile body such that the outer surface deliberately evinces a third color different from the first color and the second color; providing a core; the step of forming
  • a yet further embodiment of the invention may include a method of manufacturing a wood-plastic composite.
  • the method may include providing a first polymer, a plurality of wood fibers, a second polymer not substantially soluble in the first polymer, and an additive, melting the first polymer and the second polymer, blending the additive with the second polymer to form a blend, mixing the blend with the first polymer and the plurality of wood fibers to form a feed, forming a profile body with an outer surface from the feed, and shifting the blend towards the outer surface such that at least a portion of the blend is visible on the outer surface.
  • the invention may include one or more of the following aspects: the additive may be one or more of a pigment, a mold inhibitor, and a mildew inhibitor; the blend may substantially cover an entire side of the profile body; the additive may not be blended with either of the first polymer or the wood fibers; the additive may be soluble in the second polymer and not be soluble in the first polymer.
  • FIG. 1 is a perspective view of a composite according to an embodiment of the invention.
  • FIG. 2A is a schematic view of the composite of FIG. 1 .
  • FIG. 2B is a top schematic view of a composite according to another embodiment of the invention.
  • FIG. 2C is a top schematic view of a composite according to a further embodiment of the invention.
  • FIG. 3A is a side schematic view of the composite of FIG. 1 .
  • FIG. 3B is a side schematic view of a composite according to yet another embodiment of the invention.
  • FIG. 3C is a side schematic view of a composite according to still another embodiment of the invention.
  • FIG. 4A is a schematic view of a process of manufacturing the composite of FIG. 1 .
  • FIG. 4B is a schematic view of a process of manufacturing a composite according to a yet further embodiment of the invention.
  • FIG. 4C is a schematic view of a process of manufacturing a composite according to still another embodiment of the invention.
  • composite 1 may include a first polymer 2 , a plurality of wood fibers 3 blended with first polymer 2 to form a blend 4 , an outer surface 5 , and a second polymer 6 configured to resist blending with first polymer 2 (e.g., second polymer 6 is not substantially soluble in first polymer 2 ). Second polymer 6 may be visible on outer surface 5 .
  • Blend 4 of first polymer 2 and wood fibers 3 may have a first color and second polymer 6 may have a second color different from the first color.
  • Composite 1 may be used as a decking component or any other suitable building material.
  • composite 1 may be used as a decking board, railing, railing post, and/or decking beam.
  • composite 1 may be used to construct any portions of homes, walkways, shelters, and/or any other desirable structure.
  • Composite 1 may include a first polymer 2 which may be a crystalline polymer 2 .
  • Crystalline polymer 2 is preferably at least one of high density polyethylene (HDPE), low density polyethylene (LDPE), linear low density polyethylene (LLDPE), and polypropylene (PP).
  • the polypropylene may be a homo- and/or a co-polymer polypropylene.
  • any crystalline polymer may be used, such as one or more polyamides (PA), nylons, polyoxymethylenes, polybutylene terephthalates (PBT), polyethylene terephthalates (PET), and/or acetals.
  • Crystalline polymer 2 may have any suitable size, shape, and/or configuration to be melted, mixed with wood fibers 3 , and/or extruded into a dimensionally stable profile. Crystalline polymer 2 may have any suitable size, shape, and/or configuration to be used in any of the apparatuses or methods disclosed in co-owned U.S. Pat. Nos. 5,851,469 and 6,527,532, co-pending and co-owned U.S. patent application Ser. No. 10/292,672 filed Nov. 12, 2002, and co-pending and co-owned U.S. patent application Ser. No. 10/668,368 filed Sep. 24, 2003, the entirety of all of which are incorporated herein by reference.
  • crystalline polymer 2 may be in the form of a pellet, a flake, a film, and/or a scrap form.
  • crystalline polymer 2 may range in size from reactor powder having a diameter of about 0.01650 inches to pieces of plastic having dimensions (e.g., length, width, height, depth, and/or diameter) between about 1 inch and about 100 feet. More typically, however, crystalline polymer 2 is film scrap having dimensions (e.g., length, width, height, depth, and/or diameter) between about 0.0787 inches and 0.25 inches.
  • Composite 1 may include a second polymer 6 which may be an amorphous polymer 6 .
  • Amorphous polymer 6 is preferably a styrenic polymer such as polystrene (PS).
  • PS polystrene
  • any amorphous polymer may be used in composite 1 , such as one or more of Impact PS, polymethylmethacrylates (PMMA), polyvinyl chlorides (PVC), acrylonitrile-butadine-styrene copolymers (ABS), thermoplastic polyurethanes (TPU), styrene acrylonitrile copolymers (SAN), polyphenyl oxide (PPO), acryla-styrene butyl-acrylate or acrylate styrene acrylonitrile (either of which may be abbreviated as ASA), and/or polycarbonates (PC).
  • PMMA polymethylmethacrylates
  • PVC polyvinyl chlorides
  • ABS acrylonitrile-but
  • Amorphous polymer 6 may have any suitable size, shape, and/or configuration.
  • amorphous polymer 6 may be in the form of pellets and/or flakes.
  • amorphous polymer 6 has a high polarity and/or decreased melt flow relative to crystalline polymer 2 .
  • the size of the amorphous polymer 6 used may be dependent on these and other properties of amorphous polymer 6 .
  • amorphous polymer 6 may be a substantially solid chunk having dimensions (e.g., length, width, diameter, depth, and/or height) between about 0.25 inches and 0.0165 inches or may have a substantially spherical shape having an average diameter of about 0.0165 inches.
  • polymers In its solid form, polymers generally are capable of forming different structures depending on the structure of the polymer chain as well as the processing conditions.
  • amorphous polymers 6 the polymer chain is substantially random and unordered in structure, while in crystalline polymers 2 , the structure of the polymer backbone is a substantially regular, ordered structure such that the polymer can be tightly packed, although in general most crystalline polymer 2 are only semicrystalline. This is because the exact make up and details of the polymer backbone will determine whether the polymer is capable of crystallizing.
  • PVC depending on the characteristics of its backbone, may be either crystalline (isotactic or syndiotactic structures) or amorphous (atactic structure).
  • amorphous polymers 6 generally cannot fit into the semicrystalline structures of crystalline polymers 2 (e.g., like incompatible puzzle pieces), and amorphous polymers 6 may also exhibit polarities that prevent it from being integrated into the semicrystalline structures of crystalline polymers 2 (e.g., like oil and water).
  • amorphous polymer 6 has a different solubility parameter then crystalline polymer 2 .
  • the polarities of amorphous polymer 6 may also allow it to retain polar pigments (e.g., which may be background color 9 ) that may not bind as well to crystalline polymer 2 which is either devoid and/or has a lower polarity than amorphous polymer 6 .
  • Composite 1 may include a plurality of wood fibers 3 .
  • Wood fibers 3 may be from any type of suitable wood, for example, one or more hardwoods and/or softwoods. Wood fibers 3 may be of any suitable shape and/or size, and may be configured to be suitably blended with crystalline polymer 2 such that a mixture or blend 4 of wood fibers 3 and crystalline polymer 2 appears substantially homogenous in color and/or consistency.
  • wood fibers 3 may have dimensions (e.g., length, width, depth, diameter, and/or height) ranging from about 6 inches to about 0.25 inches, all the way down to substantially spherical shapes having an average diameter of about 0.00079 inches.
  • wood fibers 3 may range in size from substantially spherical shapes having an average diameter of about 0.07870 inches to substantially spherical shapes having an average diameter of about 0.007 inches.
  • the wood fibers 3 may be mixed with and/or be replaced with any suitable organic or inorganic filler material, including one or more of grass, wheat hulls, corn stocks, corn ears, nuts, nut shells, peanuts, peanut shells, walnut, walnut shells, sand, clay, dirt, and concrete.
  • Second polymer 6 may resist blending with first polymer 2 (e.g., second polymer 6 may not be soluble in first polymer 2 and vice versa).
  • second polymer 6 is an amorphous polymer and first polymer 2 is a crystalline polymer, even when both polymers are in a melted state, the two polymers may resist blending with each other.
  • amorphous polymer 6 may be somewhat dispersed throughout crystalline polymer 2
  • amorphous polymer 6 may not be evenly distributed or blended throughout crystalline polymer 2 (e.g., amorphous polymer 6 may migrate to the outer surface 5 ).
  • amorphous polymer 6 may form “clumps” and/or “pockets” in crystalline polymer 2 , and thus regions of amorphous polymer 6 may be clearly discernible in the otherwise substantially homogenous blend of crystalline polymer 2 and wood fibers 3 .
  • amorphous polymer 6 may have a different color and/or consistency than any combination of crystalline polymer 2 and wood fibers 3 .
  • Composite 1 may have a variegated outer surface 5 (i.e., a first portion of outer surface 5 may have a first color and a second portion of outer surface 5 may have a second color different from the first color).
  • outer surface 5 may include streaks 16 .
  • Streaks 16 may run in any direction, may have any size and/or shape, may be disposed in and/or on any portion of composite 1 , may have any configuration, and/or may have a color different from the rest of composite 1 .
  • streaks 16 may assist composite 1 in obtaining a more aesthetically pleasing wood-like appearance.
  • Streaks 16 are preferably present toward outer surface 5 . Any surface of composite 1 , for example inner surfaces of composite 1 , may have streaks 16 .
  • amorphous polymer 6 may be responsible for streaks 16 on outer surface 5 of composite 1 .
  • amorphous polymer 6 may be dispersed in the blend (e.g., mixed but not blended with the blend) such that streaks 16 correspond to the location of amorphous polymer 6 .
  • amorphous polymer 6 is preferably disposed toward outer surface 5 of composite 1 .
  • Composite 1 may have an outer surface 5 that includes 50% or more of second polymer 6 (e.g., more than 50% of the surface area of outer surface 5 of composite 1 may be second polymer 6 ).
  • substantially entire portions of outer surface 5 e.g., one or more of the top, bottom, sides, and/or ends of composite 1
  • composite 1 may appear as is if it was coextruded such that second polymer 6 substantially surrounds first polymer 2 .
  • entire portions of outer surface 5 may appear to have substantially one color (e.g., the color of second polymer 6 after it has been extruded using any of the exemplary methods set forth herein), even though composite 1 may include one or more components (e.g., first polymer 2 , wood fibers 3 , blend 4 , second polymer 6 , background color 9 , and/or blend 18 ) having different colors either prior to, during, or following processing.
  • first polymer 2 wood fibers 3 , blend 4 , second polymer 6 , background color 9 , and/or blend 18
  • Amorphous polymer 6 may have a melting temperature that is substantially the same as a melting temperature of crystalline polymer 2 , as shown in the following table: Polymer Melting Temperature Range (° C.) HDPE 125°-132° LLDPE 110°-125° LDPE 103°-110° PP-Homo 160°-175° PP-Copolymer 150°-175° PS 74°-105° ABS 88°-125° SAN 100°-200° PS-Rubber Mod. 93°-105°
  • non-melting mixing e.g., mixing without blending
  • the present invention has the advantage that even though the polymers used (e.g., crystalline polymer 2 and amorphous polymer 6 ) may have substantially the same melting temperature, the two polymers will still resist blending.
  • Composite i may include a third polymer 7 .
  • third polymer 7 may be an amorphous polymer.
  • Third polymer 7 may be the same amorphous polymer as second polymer 6 , or may be a different amorphous polymer.
  • Third polymer 7 may have the same color as second polymer 6 , or may have a different color.
  • Third polymer 7 may behave similarly to second polymer 6 .
  • third polymer 7 may form streaks 16 on outer surface 5 of composite 1 that have a color different from the rest of outer surface 5 .
  • composite 1 may have a plurality of streaks against a base background color of composite 1 , with a first set 16 A of streaks 16 having a first color and second set 16 B of streaks 16 having a second color different from the first color.
  • composite 1 may include any suitable number of crystalline polymers, wood fiber types, and/or amorphous polymers.
  • amorphous polymers cover substantially entire portions of composite 1 (e.g., as set forth in FIG. 3C )
  • composite 1 may still evince more than color, for example, one color may correspond to the presence of amorphous polymer 6 on some portions of outer surface 5 while another color may correspond to the presence of amorphous polymer 7 on other portions of outer surface 5 .
  • composite 1 may include a core 8 .
  • Core 8 may have any suitable size, shape, configuration, and/or composition. Core 8 may be configured to impart strength or any other suitable property to composite 1 .
  • Core 8 may itself be a wood-plastic composite.
  • the mixture of crystalline polymer 2 , amorphous polymer 6 , and/or wood fibers 3 may be disposed around core 8 and/or integrated (e.g., fused) with core 8 .
  • Composite 1 may include a background color 9 and/or pigment.
  • Background color 9 may be configured to color one or more of crystalline polymer 2 , amorphous polymer 6 , amorphous: polymer 7 , and/or wood fibers 3 .
  • background color 9 may be processed with crystalline polymer 2 and/or wood fiber 3 such that background color 9 permeates crystalline polymer 2 and/or wood fiber 3 and forms blend 4 (e.g., background color 9 may permeate associate/engage with portions of the polymer chain of crystalline polymer 2 ).
  • blend 4 may then be processed with amorphous polymer 6 in a suitable manner such that background color 9 does not substantially permeate amorphous polymer 6 .
  • the processing of blend 4 and amorphous polymer 6 may occur at a lower temperature than the processing of background color 9 , crystalline polymer 2 , and/or wood fiber 3 .
  • the aforementioned structures of the respective polymer chains of crystalline polymer 2 and amorphous polymer 6 may be substantially incompatible and/or resistant to blending (e.g., at any temperature). Accordingly, background color 9 may substantially remain attached to/within crystalline polymer 2 and/or blend 4 and not appreciably permeate amorphous polymer 6 .
  • background color 9 may be added to amorphous polymer 6 in addition to and/or instead of crystalline polymer 2 , and any of the aforementioned characteristics may be applicable to amorphous polymer 6 (e.g., because amorphous polymer 6 and crystalline polymer 2 are configured to resist blending, background color 9 will substantially remain associated with amorphous polymer 6 and not crystalline polymer 2 ). Indeed, adding background color 9 to amorphous polymer 6 and then mixing amorphous polymer 6 (which already has been mixed with background color 9 ) with either a colored or uncolored blend 4 is the preferred embodiment. Background color 9 may have a polarity that increases the likelihood that background color 9 will remain associated with amorphous polymer 6 .
  • background color 9 and amorphous polymer 6 may have polarities that may cause them to be attracted to each other like magnets with opposing polarities
  • crystalline polymer 2 e.g., background color 9 and crystalline polymer 2 may have polarities that may cause them to repel each other like magnets with substantially the same polarities
  • composite 1 may include another material, compound, and/or additive intermixed with at least one of crystalline polymer 2 and amorphous polymer 6 , for example, in substantially the same way as background color 9 is intermixed with at least one of crystalline polymer 2 and amorphous polymer 6 as set forth herein, and especially in the previous paragraph.
  • the another material may include a compound that, either on its own or when mixed with at least one of crystalline polymer 2 and amorphous polymer 6 , causes at least portions of composite 1 (and preferably outer surface 5 of composite 1 ) to be resistant to molding and/or mildewing (e.g., keeps the level of microorganisms, mildew, and/or mold in and/or on a composite 1 lower than about 0.1 parts per million).
  • Such a material may include a dichloro-octyl-isothiazolone (DCOIT) biostabilizer (e.g., biocide), such as certain grades of VINYZENETM manufactured by ROHM AND HAASTM (or other isothiazolones), however, any other suitable material (e.g., biostabiliter or biocide) that prevents and/or reduces molding and/or mildewing either alone or when mixed with at least one of crystalline polymer 2 and amorphous polymer 6 is also acceptable.
  • DCOIT dichloro-octyl-isothiazolone
  • Examples of acceptable methods for determining whether a particular material may include American Association for Testing Materials (ASTMTM) standards ASTMTM D-1413-99 SOIL-BLACK, ASTMTM D-4445-91 SAP STAIN, ASTMTM E-1428-99 PINK STAIN, ASTMTM G-21-96 MIXED FUNGI, ASTMTM D-5583-00 SINGLE CULTURE, and/or MILITARY STANDARD 810-E HUMIDITY CHAMBER, and/or their equivalents.
  • ASTMTMTM D-1413-99 SOIL-BLACK ASTMTM D-4445-91 SAP STAIN
  • ASTMTM E-1428-99 PINK STAIN ASTMTM G-21-96 MIXED FUNGI
  • ASTMTM D-5583-00 SINGLE CULTURE ASTMTM D-5583-00 SINGLE CULTURE
  • MILITARY STANDARD 810-E HUMIDITY CHAMBER and/or their equivalents.
  • the another material such as the DCOIT biostabilizer
  • the another material such as the DCOIT biostabilizer
  • the DCOIT biostabilizer (examples of which may include VINYZENETM IT 4000 Series, VINYZENETM IT 4010 Series, and VINYZENETM SB 27, all of which are manufactured by ROHM AND HAASTM) may be dispersed throughout the crystalline polymer 2 , but preferably the amorphous polymer 6 , in any concentration suitable to prevent or reduce mold or mildew growth on the composite 1 , for example, between about 800 parts per million and about 2000 parts per million and/or between about 1000 parts per million and 1200 parts per million.
  • the DCOIT biostabilizer may have a thermal stability of about 220° C. and/or a solubility in water of about 6 parts per million.
  • a suitable biostabilizer may be 10.10′-oxybisphenoxarsine (OBPA), examples of which may include VINYZENETM BP 5-2 Series, VINYZENETM BP 5-5 Series, VINYZENETM SB 1, and VINYZENETM SB 1 Series.
  • the OBPA biostabilizer may be dispersed throughout the crystalline polymer 2 , but preferably the amorphous polymer 6 , in any concentration suitable to prevent or reduce mold or mildew growth on the composite 1 , for example, between about 200 parts per million and about 500 parts per million.
  • the OBPA biostabilizer may have a thermal stability of about 300° C. and/or a solubility in water of about 6 parts per million.
  • a further example of a suitable biostabilizer may be octyl-isothiazoline (OIT), examples of which may include VINYZENETM IT 3000 Series, VINYZENETM IT 3010 Series, VINYZENETM IT 3025 DIDP, and VINYZENETM SB 8.
  • the OIT biostabilizer may be dispersed throughout the crystalline polymer 2 , but preferably the amorphous polymer 6 , in any concentration suitable to prevent or reduce mold or mildew growth on the composite 1 , for example, between about 800 parts per million and about 1200 parts per million.
  • the OIT biostabilizer may have a thermal stability of about 220° C. and/or a solubility in water of about 500 parts per million.
  • a suitable biostabilizer may be trichlorophenoxyphenol (TCPP), examples of which may include VINYZENETM SB 30.
  • TCPP biostabilizer may be dispersed throughout the crystalline polymer 2 , but preferably the amorphous polymer 6 , in any concentration suitable to prevent or reduce mold or mildew growth on the composite 1 , for example, between about 800 parts per million and about 1200 parts per million.
  • the TCPP biostabilizer may have a thermal stability of about 230° C. and/or a solubility in water of about 10 parts per million.
  • a yet further example of a suitable biostabilizer includes biostabilizers that prevent and/or reduce the growth of any of the following exemplary fungi, bacteria, and/or actinomycetes on composite 1 : Alternaria, Aureobasidium, Curvularia, Aspergillus, Penicillium, Fusarium, Bigrospora, Chaetomium, Gliocladium, Helminthsporium, and/or all of the subspecies of the aforementioned fungi, bacteria, and/or actinomycetes.
  • biostabilizer e.g., biocide
  • biostabilizers having one or more of the following features: substantially non-toxic; safe and environmentally friendly; broad spectrum; compatibility with formulation; leach and ultraviolet resistant; has sufficient thermal stability; and ease of use and handling.
  • a still further example of a suitable biostabilizer may include zinc borate, which may be in the form of a crystalline powder having a solubility in water of about 2800 parts per million and a particle sizes between about 1-2 microns.
  • biostabilizers e.g., biocides
  • methods for determining suitable biostabilizers for wood-plastic and other composites were disclosed in a presentation entitled Maintaining the Aesthetic Quality of WPC Decking with Isothiazolone Biocide by Peter Dylingowski, which was presented on May 20, 2003 at the 7 th International Conference on Wood-Fiber Plastic Composites, the entirety of which is incorporated herein by reference.
  • An exemplary embodiment of the invention includes a method of manufacturing a wood-plastic composite. As shown in FIGS. 4A-4C , the method may include providing a first polymer 2 , providing a plurality of wood fibers 3 , providing a second polymer 6 configured to resist blending with first polymer 2 , melting first polymer 2 , melting second polymer 6 , mixing second polymer 6 with first polymer 2 and wood fibers 3 to form a feed 10 , and forming a profile body 1 .
  • Profile body 1 may include an outer surface 5 deliberately evincing a first color and a second color different from the first color.
  • Profile body 1 may also include an outer surface 5 being substantially composed of second polymer 6 , with a cross-sectional profile of profile body 1 showing that a layer of second polymer 6 may be substantially disposed around blend 4 of first polymer 2 and wood fibers 3 .
  • First polymer 2 may include a crystalline polymer 2 .
  • Crystalline polymer 2 is preferably at least one of high density polyethylene (HDPE), low density polyethylene (LDPE), linear low density polyethylene (LLDPE), and polypropylene (PP), however, any crystalline polymer may be used in composite 1 , such as one or more polyamides (PA), nylons, polyoxymethylenes, polybutylene terephthalates (PBT), polyethylene terephthalates (PET);.and/or acetals.
  • First polymer 2 may be provided in any suitable form (e.g., pellets, flakes, sheets, etc.) to be melted, mixed with wood fibers 3 , and/or extruded into a dimensionally stable profile.
  • First polymer 2 may have any suitable size, shape, and/or configuration to be used in any of the apparatuses or methods disclosed in co-owned U.S. Pat. Nos. 5,851,469 and 6,527,532, co-pending and co-owned U.S. patent application Ser. No. 10/292,672 filed Nov. 12, 2002, and co-pending and co-owned U.S. patent application Ser. No. 10/668,368 filed Sep. 24, 2003, the entirety of all of which are incorporated herein by reference.
  • First polymer 2 may be processed prior to extruding the feed 10 using any suitable method. For example, first polymer 2 may be chopped, purified, shredded, heated, and/or demoistured. In various embodiments, first polymer 2 may be heated (e.g., by shear friction with the apparatus or by the application of external thermal energy) to completely melt, partially melt, and/or improve processability.
  • Crystalline polymers 2 may be selected because they have a specific color (e.g., be mixed with a certain color dye) and/or composition (e.g., allows background color 9 to suitable permeate its structure). However, because crystalline polymers 2 (and/or its additives such as background color 9 ) tend to blend and form a substantially homogenous color, the specific colors and/or compositions of crystalline polymers 2 used in the process need not be tightly controlled. Some specific dyes may affect the resulting color of profile body 1 more than other dyes.
  • One of ordinary skill in the art may control crystalline polymers 2 input into the process in order to achieve the desired resultant color for outer surface 5 .
  • Crystalline polymer 2 may have any suitable size, shape, and/or configuration, exemplary parameters for which have already been set forth herein.
  • Second polymer 6 may include an amorphous polymer.
  • Amorphous polymer 6 is preferably a styrenic polymer such as polystrene (PS), however, any amorphous polymer may be used in composite 1 , such as one or more of Impact PS, polymethylmethacrylates (PMMA), polyvinyl chlorides (PVC), acrylonitrile-butadine-styrene copolymers (ABS), thermoplastic polyurethanes (TPU), styrene acrylonitrile copolymers (SAN), polyphenyl oxide (PPO), acryla-styrene butyl-acrylate or acrylate styrene acrylonitrile (either of which may be abbreviated as ASA), and/or polycarbonates (PC).
  • PMMA polymethylmethacrylates
  • PVC polyvinyl chlorides
  • ABS acrylonitrile-butadine-styrene copolymers
  • TPU
  • Second polymer 6 may be provided in any suitable form (e.g., pellets, flakes, sheets, films, etc.) Second polymer 6 may be processed prior to extruding the feed 10 using any suitable method. For example, second polymer 6 may be chopped, shredded, heated, purified, and/or demoistured. In another example, background color may be added to second polymer 6 , and then second polymer 6 may introduced into a processing apparatus, such as extruder 15 , substantially cold (e.g., without processing) to be mixed with blend 4 and/or into the processing apparatus as close to the extruder die 19 of the processing apparatus as possible to be extruded with blend 4 .
  • a processing apparatus such as extruder 15 , substantially cold (e.g., without processing) to be mixed with blend 4 and/or into the processing apparatus as close to the extruder die 19 of the processing apparatus as possible to be extruded with blend 4 .
  • Amorphous polymer 6 used may be selected based on its color and/or composition.
  • Amorphous polymer 6 may have an initial color and/or resultant color that is different from the initial color and/or resultant color of the one or more crystalline polymers (with or without wood fibers 3 ) that amorphous polymer 6 is being mixed with.
  • crystalline polymers 2 after processing (with or without wood fibers 3 and/or background color 9 ), may result in a substantially gray color
  • amorphous polymer 6 after processing, may result in a substantially black color.
  • Amorphous polymer 6 may have any suitable size, shape, and/or configuration.
  • amorphous polymer 6 may be provided in flake or pellet form.
  • Crystalline polymer 2 and/or amorphous polymer 6 may be melted using any suitable method.
  • crystalline polymer 2 and/or amorphous polymer 6 may be heated using in an external heat source (e.g., a flame in a heater 13 ) or may be heated through kinetic energy (e.g., by passing through a barrel 12 with a rotating screw 11 , or passing through extruder die 19 ).
  • Crystalline polymer 2 and/or amorphous polymer 6 may be melted at any point in the composite manufacturing process prior to forming profile body 1 .
  • Crystalline polymer 2 and/or amorphous polymer 6 may be heated separately and/or together.
  • crystalline polymer 2 and/or wood-fibers 3 may be heated and blended to form blend 4 .
  • Crystalline polymer 2 may be heated substantially throughout crystalline polymer 2 and/or enough to improve processability (e.g., mixing and/or blending).
  • Wood fibers 3 may be from any type of suitable wood, for example, one or more hardwoods and/or softwoods. Wood fibers 3 may also be mixed with and/or replaced by any organic or inorganic filler such as those set forth herein. Wood fibers 3 may be of any suitable shape and/or size, and may be configured to be suitably blended with crystalline polymer 2 such that a mixture of wood fibers. 3 and crystalline polymer 2 appears substantially homogenous in color. Wood fibers 3 may be processed prior to forming profile body 1 using any suitable method. For example, wood fibers 3 may be chopped, shredded, heated, purified, and/or demoisturized. Wood fibers 3 may be dried prior to being blended with crystalline polymer 2 to form blend 4 . In some cases, pieces of wood fiber 3 may be discernible in blend 4 , however, wood fiber 3 will still typically have the same homogenous color as the rest of blend 4 .
  • Crystalline polymer 2 may be blended in a processor 13 with wood fibers 3 such that blend 4 is substantially homogenous.
  • blend 4 may have one substantially solid color and/or have a substantially uniform consistency.
  • Blend 4 may be formed using any suitable method.
  • Crystalline polymer 2 and wood fibers 3 may be blended by placing them together either before, during, or after crystalline polymer 2 and/or wood fibers 3 are dried.
  • Crystalline polymer 2 and wood fibers 3 may be blended using applied heat and/or mechanical agitation. Such blending may be accomplished by an extruder, high shear device, and/or a low shear mixer with or without the application of heat.
  • Second polymer 6 may be mixed with first polymer 2 and wood fibers 3 to form a feed 10 in any suitable order, any suitable ratio, and using any suitable method.
  • first polymer 2 , second polymer 6 , and plurality of wood fibers 3 may be mixed as they are advanced by one or more screws 11 in a barrel 12 and/or extruded through die 19 .
  • Second polymer 6 may be mixed with first polymer 2 and wood fibers 3 at any time prior to extruding the feed and in any relative order.
  • first polymer 2 may be blended with wood fibers 3 , the blend may be heated, and then second polymer 6 may be added to the blend.
  • first polymer 2 , second polymer 6 , and wood fibers 3 may be combined at substantially the same time and mixed simultaneously.
  • Second polymer 6 may be mixed with first polymer 2 and wood fibers 3 such that the mixture does not blend.
  • the mixture may be heated to a temperature that allows mixing but not blending.
  • second polymer 6 may be added to blend 4 to form feed 10 just prior to extruding feed 10 through extruder die 19 .
  • heating of second polymer 6 may only occur just after introducing second polymer 6 into blend 4 and/or during extrusion of feed 10 through extruder die 19 .
  • second polymer 6 may experience less of a heat history than any of first polymer 2 , wood fibers 3 , and/or blend 4 , which may assist in preventing blending.
  • first polymer 2 and second polymer 6 may assist in preventing the polymers 2 , 6 , from substantially blending.
  • Exemplary percentages of first polymer 2 , second polymer 6 , and wood fibers. 3 are listed herein, however, generally, the percentage of first polymer 2 will exceed the percentage of second polymer 6 .
  • composite 1 may include between about 100% and about 20% of crystalline polymer 2 , between about 5% and about 0% of amorphous polymer 6 , and between about 0% and about 80% wood fiber or other filler. In a preferred embodiment, composite 1 may include between about 60% and about 53% of crystalline polymer 2 , about 2% of amorphous polymer 6 , and between about 45% and about 38% wood fiber or other filler
  • composites 1 discussed herein may have other advantages.
  • composite 1 may be less susceptible to mold and mildew and/or may be more durable.
  • Crystalline polymer 2 and amorphous polymer 6 do not blend in composites 1 .
  • the minor component in this case, amorphous polymer 6
  • the minor component may migrate to the outer surface 5 of composite 1 .
  • the minor component may tend to coat at least portions of outer surface 5 (e.g., top, bottom, and/or side surfaces) with a polymer rich coating that does not absorb moisture, and thus allows outer surface 5 to resist molding and/or mildewing.
  • additional additives such as mold and mildew resistant compounds (e.g., DCOIT biostabilizers or other suitable anti-fungi bacteria materials/compounds, examples of which are set forth herein, or other materials having other desirable properties for composite 1 ), may be added to amorphous polymer 6 at any point before or during the manufacturing process of composite 1 .
  • the additive and amorphous polymer 6 may be processed so as to substantially disperse the additive through the matrix of amorphous polymer 6 .
  • amorphous polymer 6 may migrate to outer surface 5 of composite 1 , amorphous polymer 6 with mildew resistant additives (or other materials) may coat at least portions of outer surface 5 .
  • This type of delivery of the mold and mildew resistant materials and/or compounds, examples of which are set forth herein, (or other compounds with other desirable properties) to specific portions of composite 1 may have many advantages.
  • the compounds themselves may be relatively expensive and/or including too much of the compound in composite 1 may compromise some structural and/or aesthetic properties of composite 1 .
  • mildew and/or mold resistant compounds examples of which are set forth herein
  • such compounds may be most effective on at least portions of outer surface 5 of composite 1 .
  • first polymer 2 e.g., crystalline polymer
  • second polymer 6 e.g., amorphous polymer
  • second polymer 6 may be used as a vehicle to deliver desirable compounds on and/or toward outer surface 5 .
  • second polymer 6 with the desirable compound may be disposed along entire portions of outer surface 5 , for example, as set forth in FIG. 3C .
  • Profile body 1 with an outer surface 5 may be formed using any suitable method.
  • the mixture including first polymer 2 (e.g., crystalline polymer), second polymer 6 (e.g., amorphous polymer), and wood fibers 3 may be extruded through a die 19 to form profile body 1 .
  • Feed 10 may be extruded using either a single screw extruder or a double screw extruder to form profile body 1 .
  • Feed 10 may also be formed into profile body 1 using any suitable method.
  • Outer surface 5 of profile body 1 may be variegated.
  • Streaks 16 may be formed on outer surface 5 of profile body 1 .
  • the chemical properties of the two polymers and/or the processing conditions e.g., temperature, extrusion rate, mixing rate that the two polymers are subjected to
  • the processing conditions e.g., temperature, extrusion rate, mixing rate that the two polymers are subjected to
  • clumps” or “pockets” of amorphous polymer 6 may be dispersed through crystalline polymer 2 and vice versa.
  • amorphous polymer 6 may tend to go towards outer surface 5 of profile body 1 , for example, due the pressures exerted on feed 10 during extrusion.
  • the polymer chain of amorphous polymer 6 cannot interlock easily with the polymer chain and/or matrix of crystalline polymer 2 . Accordingly, amorphous polymer 6 may tend to separate from the polymer matrix of crystalline polymer 2 and go to outer surface 5 so as to form its own solid polymer matrix of amorphous polymer 6 .
  • amorphous polymer 6 may have a different initial color and/or different resultant color as the rest of profile body 1 (i.e., blend 4 of crystalline polymer 2 and wood fibers 3 ), streaks 16 of amorphous polymer 6 may be readily discernible on outer surface 5 .
  • Streaks 16 may be generally perpendicular to a cross-section of die 19 through which profile body 1 is extruded. However, streaks 16 may be in any direction, and have any other shape and/or configuration, for example, similar to those set forth in FIGS. 2A-2C .
  • entire portions of outer surface 5 may be composed of amorphous polymer 6 , for example, as shown in FIG. 3C .
  • the processing may have been such that amorphous polymer 6 forms “clumps” or “pockets” (e.g., as set forth in the previous paragraph) around substantially all of blend 4 so as to form a substantially solid matrix around blend 4 (e.g., with or without wood fibers 3 ).
  • Any suitable proportions of amorphous polymer 6 , crystalline polymer 2 , wood-fibers 3 , blend 4 , blend 18 , background color 9 , and another other material or compound set forth herein are contemplated as being discernible on outer surface 5 .
  • the method may also include providing another amorphous polymer 7 , melting another amorphous polymer 7 , and mixing another amorphous polymer 7 with amorphous polymer 6 , crystalline polymer 2 , and/or wood fibers 3 .
  • the step of extruding may include forming profile body 1 such that outer surface 5 deliberately evinces a third color different from the first color and the second color due to additional amorphous polymer 7 .
  • Another amorphous polymer 7 may be selected because its initial color and/or resultant color may be different from an initial color and/or resultant color of one or more of crystalline polymer 2 and/or wood fibers 3 .
  • Another amorphous polymer 7 may processed and/or behave similarly to other amorphous polymers 6 , thus, streaks 16 B of another amorphous polymer 7 may be formed on outer surface 5 of profile body 1 .
  • Streaks 16 B from another amorphous polymer 7 may be of a color different from either the base color of profile body 1 and/or the color of streaks 16 A from amorphous polymer 6 .
  • the method may also include providing a core 8 and forming profile body 1 around at least a portion of core 8 .
  • Core 8 may be a wood-plastic composite or any other suitable composite.
  • Core 8 may have a cross-sectional area smaller than a cross-sectional area of die 19 .
  • Core 8 may be fed by extruder 15 through die 19 such that core 8 advances through substantially the center of die 19 without contacting any portion of die 19 itself.
  • Extruder 15 and/or die 19 may then deposit an outer surface 5 on core 8 that has more than one color (e.g., variegated and/or streaked) using one or more of the methods set forth herein.
  • the variegated surface 5 may be bonded to core 8 using any suitable method, for example, when variegated surface 5 is co-extruded onto core 8 , a portion of core 8 may melt and intermix with variegated surface 5 such that core 8 and the variegated surface 5 are substantially fused. Accordingly, the resultant product may be a building material with a core 8 having a wood-plastic composite having a deliberately variegated outer surface 5 formed around it. Such a resultant product may be desirable, for example, to impart strength to the component (e.g., by providing a core component having a high strength such as aluminum or steel).
  • the method also may include the use of a background color 9 .
  • background color 9 may be added to crystalline polymer 2 and/or wood fiber 3 (e.g., blend 4 ) to impart a color to blend 4 different from an initial color of blend 4 , crystalline polymer 2 , and/or wood fiber 3 .
  • Background color 9 , crystalline polymer 2 , wood fibers 3 , and/or blend 4 may be processed by processor 13 using any suitable apparatus and/or method to form resultant blend 4 .
  • Resultant blend 4 may then be transferred to extruder 15 and processed with amorphous polymer 6 to form profile body 1 with streaks 16 or other variations of outer surface 5 as set forth herein.
  • Background color 9 may be added to any step of the process and/or any component or subcomponent of the process at any time prior to extrusion through die 19 .
  • background color 9 may be added to amorphous polymer 6 to impart a color to amorphous polymer 6 different from an initial color of amorphous polymer 6 .
  • Background color 9 and/or amorphous polymer 6 may be processed by processor 17 using any suitable apparatus and/or method to form resultant blend 18 of amorphous polymer 6 and background color 9 .
  • Resultant blend 18 may then be transferred to extruder 15 and processed with crystalline polymer 2 , wood fibers 3 , and/or blend 4 to form profile body 1 with streaks 16 or other variations of outer surface 5 as set forth herein.
  • background color 9 may be added to any step of the process and/or any component or subcomponent of the process at any time prior to extrusion through die 19 .
  • composite 1 with streaks having multiple colors may also include a core.
  • crystalline polymer 2 and wood fibers need not be blended prior to mixing them with amorphous polymer 6 .

Landscapes

  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Wood Science & Technology (AREA)
  • Materials Engineering (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Organic Chemistry (AREA)
  • Compositions Of Macromolecular Compounds (AREA)
  • Dry Formation Of Fiberboard And The Like (AREA)

Abstract

Embodiments of the invention include a composite. The composite includes a crystalline polymer, a plurality of wood fibers blended with the crystalline polymer, an outer surface, and an amorphous polymer visible on the outer surface. The amorphous polymer has a first color and the blend of the crystalline polymer and the plurality of wood fibers has a second color different from the first color. The invention also includes a method of manufacturing the wood-plastic composites such that one polymer is shifted in the composite relative to the other polymer.

Description

    DESCRIPTION OF THE INVENTION
  • 1. Field of the Invention
  • The invention is directed to variegated wood-plastic composites and methods of manufacturing the same. For example, the surfaces of the wood-plastic composites may be variegated by varying the polymer composition of the wood-plastic composite. The invention also includes a method of manufacturing the wood-plastic composites such that one polymer is shifted in the composite relative to the other polymer.
  • 2. Background of the Invention
  • Wooden components are commonly used in manufacturing decks and related assemblies. Wooden components includes strings of wood fibers having various colors (e.g., rings on trees) that give the surface of the wooden component a streaked appearance. The streaked appearance imparts an aesthetically pleasing look and feel to the deck component. One disadvantage of using wooden components, however, is that the wood may be susceptible to rotting, weather, insects, and/or wear and tear, and may require the acquisition and processing of wood which may involve environmentally unfriendly processing techniques, such as the clear cutting of forests and the use of hazardous chemicals.
  • A more environmentally friendly alternative to using wooden components in manufacturing decks and related assemblies is to use a wood-plastic composite made of crystalline polymers. Examples of suitable wood-plastic composites made of crystalline polymers and related methods of manufacture are disclosed in co-owned U.S. Pat. Nos. 5,851,469 and 6,527,532, co-pending and co-owned U.S. patent application Ser. No. 10/292,672 filed Nov. 12, 2002, and co-pending and co-owned U.S. patent application Ser. No. 10/668,368 filed Sep. 24, 2003, the entirety of all of which are incorporated herein by reference.
  • Wood-plastic composites made of crystalline polymers, however, tend to have solid one color surfaces. This is at least partially due to the sharp melting point temperatures of crystalline polymers and the tendency of crystalline polymers to easily blend together. Thus, even if a plurality of crystalline polymers having a plurality of different colors are used to manufacture a wood-plastic composites, the plurality of different colors will blend together in the manufacturing process and the composite will emerge having a surface with one solid color. In any case, the resultant composite does not have a streaked appearance.
  • SUMMARY OF THE INVENTION
  • An exemplary embodiment of the invention includes a composite. The composite comprises a crystalline polymer, a plurality of wood fibers blended with the crystalline polymer, an outer surface, and an amorphous polymer visible on the outer surface. The amorphous polymer has a first color and the blend of the crystalline polymer and the plurality of wood fibers has a second color different from the first color.
  • In various embodiments, the invention may include one or more of the following aspects: the crystalline polymer may be at least one of polypropylene and polyethylene; the amorphous polymer may be a styrenic polymer; the outer surface may include streaks of the first color; the amorphous polymer may have a melting temperature that is substantially the same as a melting temperature of the crystalline polymer; the outer surface may be variegated; a first portion of the outer surface may have the first color and a second portion of the outer surface may have the second color; another amorphous polymer visible on the outer surface; the another amorphous polymer may have a third color different from the first color and the second color; the composite may be at least one of a building material, a decking material, and a decking board; a colorant may be blended with one of the crystalline polymer and the amorphous polymer.
  • Another embodiment of the invention includes a composite. The composite may include a first polymer, a plurality of wood fibers blended with the first polymer, an outer surface, and a second polymer configured to resist blending with the first polymer. The composite may be manufactured such that the second polymer is deliberately visible on the outer surface. The blend of the first polymer and the plurality of wood fibers may have a first color and the second polymer may have a second color different from the first color. The second polymer may not be substantially soluble in the first polymer.
  • In various embodiments, the invention may include one or more of the following aspects: the first polymer may be at least one of polypropylene and polyethylene; the second polymer may be a styrenic polymer; the outer surface may include streaks of the second color; the first polymer may have a melting temperature that is substantially the same as a melting temperature of the second polymer; the outer surface may be variegated; a first portion of the outer surface may have the first color and a second portion of the outer surface has the second color; a third polymer may be configured to resist blending with the first polymer; the composite may be manufactured such that the third polymer is deliberately visible on the outer surface; the third polymer may have a third color different from the first color and the second color; the composite may be at least one of a building material, a decking material, and a decking board; a colorant blended with one of the first polymer and the second polymer.
  • A further embodiment of the invention may include a method of manufacturing a wood-plastic composite. The method may include providing a crystalline polymer, providing a plurality of wood fibers, providing an amorphous polymer, melting the crystalline polymer, melting the amorphous polymer, mixing the amorphous polymer with the crystalline polymer and the plurality of wood fibers to form a feed, and forming a profile body from the feed, the profile body including an outer surface evincing a first color and a second color different from the first color.
  • In various embodiments, the invention may include one or more of the following aspects: forming streaks of the first color on the outer surface; forming streaks of the amorphous polymer on the outer surface; shifting the amorphous polymer towards the outer surface; variegating the outer surface; providing at least one of a single screw extruder and a double screw extruder; the step of extruding may include extruding the feed via the at least one of the single-screw extruder and the double screw extruder; the step of mixing may include forming the first color from the amorphous polymer and forming the second color from a blend of the crystalline polymer and the plurality of wood fibers; providing another amorphous polymer, melting the another amorphous polymer; mixing the another amorphous polymer with the amorphous polymer, the crystalline polymer, and the plurality of wood fibers; the step of extruding may include forming the profile body such that the outer surface evinces a third color different from the first color and the second color; providing a core; the step of forming the profile body may include forming the profile body around at least a portion of the core; providing a colorant; blending the colorant with one of the crystalline polymer and the amorphous polymer.
  • Yet another embodiment of the invention may include a method of manufacturing a wood-plastic composite. The method may include providing a first polymer, providing a plurality of wood fibers, providing a second polymer not substantially soluble in the first polymer, melting the first polymer, melting the second polymer, mixing the second polymer with the first polymer and the plurality of wood fibers to form a feed, and forming a profile body from the feed, the profile body including an outer surface deliberately evincing a first color and a second color different from the first color.
  • In various embodiments, the invention may include one or more of the following aspects: forming streaks of the first color on the outer surface; forming streaks of the first polymer on the outer surface; shifting the first polymer towards the outer surface; variegating the outer surface; providing at least one of a single screw extruder and a double screw extruder; the step of extruding may include extruding the feed via the at least one of the single-screw extruder and the double screw extruder; the step of mixing may include forming the first color from the first polymer and forming the second color from a blend of the second polymer and the plurality of wood fibers; providing a third polymer not substantially soluble in the first polymer; melting the third polymer; mixing the third polymer with the first polymer, the second polymer, and the plurality of wood fibers; the step of extruding may include forming the profile body such that the outer surface deliberately evinces a third color different from the first color and the second color; providing a core; the step of forming the profile body may include forming the profile body around at least a portion of the core; providing a colorant; blending the colorant with one of the first polymer and the second polymer.
  • A yet further embodiment of the invention may include a method of manufacturing a wood-plastic composite. The method may include providing a first polymer, a plurality of wood fibers, a second polymer not substantially soluble in the first polymer, and an additive, melting the first polymer and the second polymer, blending the additive with the second polymer to form a blend, mixing the blend with the first polymer and the plurality of wood fibers to form a feed, forming a profile body with an outer surface from the feed, and shifting the blend towards the outer surface such that at least a portion of the blend is visible on the outer surface.
  • In various embodiments, the invention may include one or more of the following aspects: the additive may be one or more of a pigment, a mold inhibitor, and a mildew inhibitor; the blend may substantially cover an entire side of the profile body; the additive may not be blended with either of the first polymer or the wood fibers; the additive may be soluble in the second polymer and not be soluble in the first polymer.
  • Additional objects and advantages of the invention will be set forth in part in the description which follows, and in part will be obvious from the description, or may be learned by practice of the invention. The objects and advantages of the invention will be realized and attained by means of the elements and combinations particularly pointed out in the appended claims.
  • It is to be understood that both the foregoing general description and the following detailed description are exemplary and explanatory only and are not restrictive of the invention, as claimed.
  • BRIEF DESCRIPTION OF THE DRAWINGS
  • The accompanying drawings, which are incorporated in and constitute a part of this specification, illustrate several embodiments of the invention and together with the description, serve to explain the principles of the invention.
  • FIG. 1 is a perspective view of a composite according to an embodiment of the invention.
  • FIG. 2A is a schematic view of the composite of FIG. 1.
  • FIG. 2B is a top schematic view of a composite according to another embodiment of the invention.
  • FIG. 2C is a top schematic view of a composite according to a further embodiment of the invention.
  • FIG. 3A is a side schematic view of the composite of FIG. 1.
  • FIG. 3B is a side schematic view of a composite according to yet another embodiment of the invention.
  • FIG. 3C is a side schematic view of a composite according to still another embodiment of the invention.
  • FIG. 4A is a schematic view of a process of manufacturing the composite of FIG. 1.
  • FIG. 4B is a schematic view of a process of manufacturing a composite according to a yet further embodiment of the invention.
  • FIG. 4C is a schematic view of a process of manufacturing a composite according to still another embodiment of the invention.
  • DESCRIPTION OF THE EMBODIMENTS
  • Reference will now be made in detail to the exemplary embodiments of the invention, examples of which are illustrated in the accompanying drawings. Wherever possible, the same reference numbers will be used throughout the drawings to refer to the same or like parts.
  • An exemplary embodiment of the invention includes a composite. As shown in FIGS. 1, 2A-2C, and 3A-3C, composite 1 may include a first polymer 2, a plurality of wood fibers 3 blended with first polymer 2 to form a blend 4, an outer surface 5, and a second polymer 6 configured to resist blending with first polymer 2 (e.g., second polymer 6 is not substantially soluble in first polymer 2). Second polymer 6 may be visible on outer surface 5. Blend 4 of first polymer 2 and wood fibers 3 may have a first color and second polymer 6 may have a second color different from the first color.
  • Composite 1 may be used as a decking component or any other suitable building material. For example, as shown in FIG. 1, composite 1 may be used as a decking board, railing, railing post, and/or decking beam. In another example, composite 1 may be used to construct any portions of homes, walkways, shelters, and/or any other desirable structure.
  • Composite 1 may include a first polymer 2 which may be a crystalline polymer 2. Crystalline polymer 2 is preferably at least one of high density polyethylene (HDPE), low density polyethylene (LDPE), linear low density polyethylene (LLDPE), and polypropylene (PP). The polypropylene may be a homo- and/or a co-polymer polypropylene. However, any crystalline polymer may be used, such as one or more polyamides (PA), nylons, polyoxymethylenes, polybutylene terephthalates (PBT), polyethylene terephthalates (PET), and/or acetals. Crystalline polymer 2 may have any suitable size, shape, and/or configuration to be melted, mixed with wood fibers 3, and/or extruded into a dimensionally stable profile. Crystalline polymer 2 may have any suitable size, shape, and/or configuration to be used in any of the apparatuses or methods disclosed in co-owned U.S. Pat. Nos. 5,851,469 and 6,527,532, co-pending and co-owned U.S. patent application Ser. No. 10/292,672 filed Nov. 12, 2002, and co-pending and co-owned U.S. patent application Ser. No. 10/668,368 filed Sep. 24, 2003, the entirety of all of which are incorporated herein by reference. For example, crystalline polymer 2 may be in the form of a pellet, a flake, a film, and/or a scrap form. In another example, crystalline polymer 2 may range in size from reactor powder having a diameter of about 0.01650 inches to pieces of plastic having dimensions (e.g., length, width, height, depth, and/or diameter) between about 1 inch and about 100 feet. More typically, however, crystalline polymer 2 is film scrap having dimensions (e.g., length, width, height, depth, and/or diameter) between about 0.0787 inches and 0.25 inches.
  • Composite 1 may include a second polymer 6 which may be an amorphous polymer 6. Amorphous polymer 6 is preferably a styrenic polymer such as polystrene (PS). However, any amorphous polymer may be used in composite 1, such as one or more of Impact PS, polymethylmethacrylates (PMMA), polyvinyl chlorides (PVC), acrylonitrile-butadine-styrene copolymers (ABS), thermoplastic polyurethanes (TPU), styrene acrylonitrile copolymers (SAN), polyphenyl oxide (PPO), acryla-styrene butyl-acrylate or acrylate styrene acrylonitrile (either of which may be abbreviated as ASA), and/or polycarbonates (PC). In a preferred embodiment, ABS is used. Amorphous polymer 6 may have any suitable size, shape, and/or configuration. For example, amorphous polymer 6 may be in the form of pellets and/or flakes. In a preferred embodiment, amorphous polymer 6 has a high polarity and/or decreased melt flow relative to crystalline polymer 2. The size of the amorphous polymer 6 used may be dependent on these and other properties of amorphous polymer 6. For example, amorphous polymer 6 may be a substantially solid chunk having dimensions (e.g., length, width, diameter, depth, and/or height) between about 0.25 inches and 0.0165 inches or may have a substantially spherical shape having an average diameter of about 0.0165 inches.
  • In its solid form, polymers generally are capable of forming different structures depending on the structure of the polymer chain as well as the processing conditions. In amorphous polymers 6, the polymer chain is substantially random and unordered in structure, while in crystalline polymers 2, the structure of the polymer backbone is a substantially regular, ordered structure such that the polymer can be tightly packed, although in general most crystalline polymer 2 are only semicrystalline. This is because the exact make up and details of the polymer backbone will determine whether the polymer is capable of crystallizing. For example, PVC, depending on the characteristics of its backbone, may be either crystalline (isotactic or syndiotactic structures) or amorphous (atactic structure). Accordingly, due to these differences in polymer structures, amorphous polymers 6 generally cannot fit into the semicrystalline structures of crystalline polymers 2 (e.g., like incompatible puzzle pieces), and amorphous polymers 6 may also exhibit polarities that prevent it from being integrated into the semicrystalline structures of crystalline polymers 2 (e.g., like oil and water). Thus, amorphous polymer 6 has a different solubility parameter then crystalline polymer 2. The polarities of amorphous polymer 6 may also allow it to retain polar pigments (e.g., which may be background color 9) that may not bind as well to crystalline polymer 2 which is either devoid and/or has a lower polarity than amorphous polymer 6.
  • Composite 1 may include a plurality of wood fibers 3. Wood fibers 3 may be from any type of suitable wood, for example, one or more hardwoods and/or softwoods. Wood fibers 3 may be of any suitable shape and/or size, and may be configured to be suitably blended with crystalline polymer 2 such that a mixture or blend 4 of wood fibers 3 and crystalline polymer 2 appears substantially homogenous in color and/or consistency. For example, wood fibers 3 may have dimensions (e.g., length, width, depth, diameter, and/or height) ranging from about 6 inches to about 0.25 inches, all the way down to substantially spherical shapes having an average diameter of about 0.00079 inches. More typically, however, wood fibers 3 may range in size from substantially spherical shapes having an average diameter of about 0.07870 inches to substantially spherical shapes having an average diameter of about 0.007 inches. In various embodiments, the wood fibers 3 may be mixed with and/or be replaced with any suitable organic or inorganic filler material, including one or more of grass, wheat hulls, corn stocks, corn ears, nuts, nut shells, peanuts, peanut shells, walnut, walnut shells, sand, clay, dirt, and concrete.
  • Second polymer 6 may resist blending with first polymer 2 (e.g., second polymer 6 may not be soluble in first polymer 2 and vice versa). For example, if second polymer 6 is an amorphous polymer and first polymer 2 is a crystalline polymer, even when both polymers are in a melted state, the two polymers may resist blending with each other. Thus, while amorphous polymer 6 may be somewhat dispersed throughout crystalline polymer 2, amorphous polymer 6 may not be evenly distributed or blended throughout crystalline polymer 2 (e.g., amorphous polymer 6 may migrate to the outer surface 5). Accordingly, amorphous polymer 6 may form “clumps” and/or “pockets” in crystalline polymer 2, and thus regions of amorphous polymer 6 may be clearly discernible in the otherwise substantially homogenous blend of crystalline polymer 2 and wood fibers 3. For example, amorphous polymer 6 may have a different color and/or consistency than any combination of crystalline polymer 2 and wood fibers 3.
  • Composite 1 may have a variegated outer surface 5 (i.e., a first portion of outer surface 5 may have a first color and a second portion of outer surface 5 may have a second color different from the first color). For example, outer surface 5 may include streaks 16. Streaks 16 may run in any direction, may have any size and/or shape, may be disposed in and/or on any portion of composite 1, may have any configuration, and/or may have a color different from the rest of composite 1. For example, streaks 16 may assist composite 1 in obtaining a more aesthetically pleasing wood-like appearance. Streaks 16 are preferably present toward outer surface 5. Any surface of composite 1, for example inner surfaces of composite 1, may have streaks 16.
  • Due to the properties of the amorphous polymer 6 set forth above, and especially with regard to its possible tendency to resist blending with crystalline polymers, amorphous polymer 6 may be responsible for streaks 16 on outer surface 5 of composite 1. For example, when melted and mixed with crystalline polymer 2 and wood fiber blend, amorphous polymer 6 may be dispersed in the blend (e.g., mixed but not blended with the blend) such that streaks 16 correspond to the location of amorphous polymer 6. As shown in FIG. 3A, amorphous polymer 6 is preferably disposed toward outer surface 5 of composite 1.
  • Composite 1 may have an outer surface 5 that includes 50% or more of second polymer 6 (e.g., more than 50% of the surface area of outer surface 5 of composite 1 may be second polymer 6). For example, as shown in FIG. 3C substantially entire portions of outer surface 5 (e.g., one or more of the top, bottom, sides, and/or ends of composite 1) may be composed of second polymer 6. Thus, in some configurations, composite 1 may appear as is if it was coextruded such that second polymer 6 substantially surrounds first polymer 2. In such a configuration, entire portions of outer surface 5 may appear to have substantially one color (e.g., the color of second polymer 6 after it has been extruded using any of the exemplary methods set forth herein), even though composite 1 may include one or more components (e.g., first polymer 2, wood fibers 3, blend 4, second polymer 6, background color 9, and/or blend 18) having different colors either prior to, during, or following processing.
  • Amorphous polymer 6 may have a melting temperature that is substantially the same as a melting temperature of crystalline polymer 2, as shown in the following table:
    Polymer Melting Temperature Range (° C.)
    HDPE 125°-132°
    LLDPE 110°-125°
    LDPE 103°-110°
    PP-Homo 160°-175°
    PP-Copolymer 150°-175°
    PS  74°-105°
    ABS  88°-125°
    SAN 100°-200°
    PS-Rubber Mod.  93°-105°

    Thus, for polymers listed above, non-melting mixing (e.g., mixing without blending) of amorphous polymer 6 and crystalline polymer 2 may occur between about 140° C. and about 180° C., depending on the exact polymers used. Thus, the present invention has the advantage that even though the polymers used (e.g., crystalline polymer 2 and amorphous polymer 6) may have substantially the same melting temperature, the two polymers will still resist blending.
  • Composite i may include a third polymer 7. For example, third polymer 7 may be an amorphous polymer. Third polymer 7 may be the same amorphous polymer as second polymer 6, or may be a different amorphous polymer. Third polymer 7 may have the same color as second polymer 6, or may have a different color. Third polymer 7 may behave similarly to second polymer 6. For example, third polymer 7 may form streaks 16 on outer surface 5 of composite 1 that have a color different from the rest of outer surface 5. Thus, composite 1 may have a plurality of streaks against a base background color of composite 1, with a first set 16A of streaks 16 having a first color and second set 16B of streaks 16 having a second color different from the first color. One of ordinary skill in the art would realize that composite 1 may include any suitable number of crystalline polymers, wood fiber types, and/or amorphous polymers. In the example where amorphous polymers cover substantially entire portions of composite 1 (e.g., as set forth in FIG. 3C), composite 1 may still evince more than color, for example, one color may correspond to the presence of amorphous polymer 6 on some portions of outer surface 5 while another color may correspond to the presence of amorphous polymer 7 on other portions of outer surface 5.
  • As shown in FIG. 3B, composite 1 may include a core 8. Core 8 may have any suitable size, shape, configuration, and/or composition. Core 8 may be configured to impart strength or any other suitable property to composite 1. Core 8 may itself be a wood-plastic composite. The mixture of crystalline polymer 2, amorphous polymer 6, and/or wood fibers 3 may be disposed around core 8 and/or integrated (e.g., fused) with core 8.
  • Composite 1 may include a background color 9 and/or pigment. Background color 9 may be configured to color one or more of crystalline polymer 2, amorphous polymer 6, amorphous: polymer 7, and/or wood fibers 3. For example, background color 9 may be processed with crystalline polymer 2 and/or wood fiber 3 such that background color 9 permeates crystalline polymer 2 and/or wood fiber 3 and forms blend 4 (e.g., background color 9 may permeate associate/engage with portions of the polymer chain of crystalline polymer 2). However, blend 4 may then be processed with amorphous polymer 6 in a suitable manner such that background color 9 does not substantially permeate amorphous polymer 6. For example, the processing of blend 4 and amorphous polymer 6 may occur at a lower temperature than the processing of background color 9, crystalline polymer 2, and/or wood fiber 3. In another example, the aforementioned structures of the respective polymer chains of crystalline polymer 2 and amorphous polymer 6 may be substantially incompatible and/or resistant to blending (e.g., at any temperature). Accordingly, background color 9 may substantially remain attached to/within crystalline polymer 2 and/or blend 4 and not appreciably permeate amorphous polymer 6.
  • In various embodiments, background color 9 may be added to amorphous polymer 6 in addition to and/or instead of crystalline polymer 2, and any of the aforementioned characteristics may be applicable to amorphous polymer 6 (e.g., because amorphous polymer 6 and crystalline polymer 2 are configured to resist blending, background color 9 will substantially remain associated with amorphous polymer 6 and not crystalline polymer 2). Indeed, adding background color 9 to amorphous polymer 6 and then mixing amorphous polymer 6 (which already has been mixed with background color 9) with either a colored or uncolored blend 4 is the preferred embodiment. Background color 9 may have a polarity that increases the likelihood that background color 9 will remain associated with amorphous polymer 6. (e.g., background color 9 and amorphous polymer 6 may have polarities that may cause them to be attracted to each other like magnets with opposing polarities) and not become associated with crystalline polymer 2 (e.g., background color 9 and crystalline polymer 2 may have polarities that may cause them to repel each other like magnets with substantially the same polarities).
  • In another embodiment, composite 1 may include another material, compound, and/or additive intermixed with at least one of crystalline polymer 2 and amorphous polymer 6, for example, in substantially the same way as background color 9 is intermixed with at least one of crystalline polymer 2 and amorphous polymer 6 as set forth herein, and especially in the previous paragraph. For example, the another material may include a compound that, either on its own or when mixed with at least one of crystalline polymer 2 and amorphous polymer 6, causes at least portions of composite 1 (and preferably outer surface 5 of composite 1) to be resistant to molding and/or mildewing (e.g., keeps the level of microorganisms, mildew, and/or mold in and/or on a composite 1 lower than about 0.1 parts per million). An example of such a material may include a dichloro-octyl-isothiazolone (DCOIT) biostabilizer (e.g., biocide), such as certain grades of VINYZENE™ manufactured by ROHM AND HAAS™ (or other isothiazolones), however, any other suitable material (e.g., biostabiliter or biocide) that prevents and/or reduces molding and/or mildewing either alone or when mixed with at least one of crystalline polymer 2 and amorphous polymer 6 is also acceptable. Examples of acceptable methods for determining whether a particular material (e.g., biostabilizer, biocide) suitably prevents and/or reduces mold and/or mildew on composite 1 may include American Association for Testing Materials (ASTM™) standards ASTM™ D-1413-99 SOIL-BLACK, ASTM™ D-4445-91 SAP STAIN, ASTM™ E-1428-99 PINK STAIN, ASTM™ G-21-96 MIXED FUNGI, ASTM™ D-5583-00 SINGLE CULTURE, and/or MILITARY STANDARD 810-E HUMIDITY CHAMBER, and/or their equivalents. Indeed, in any of the embodiments set forth herein, the another material, such as the DCOIT biostabilizer, may be substituted for background color 9 and may exhibit any of the properties of background color 9 relative to the crystalline polymer 2, amorphous polymer 6, and/or blend 4 in any portion of the process.
  • The DCOIT biostabilizer (examples of which may include VINYZENE™ IT 4000 Series, VINYZENE™ IT 4010 Series, and VINYZENE™ SB 27, all of which are manufactured by ROHM AND HAAS™) may be dispersed throughout the crystalline polymer 2, but preferably the amorphous polymer 6, in any concentration suitable to prevent or reduce mold or mildew growth on the composite 1, for example, between about 800 parts per million and about 2000 parts per million and/or between about 1000 parts per million and 1200 parts per million. The DCOIT biostabilizer may have a thermal stability of about 220° C. and/or a solubility in water of about 6 parts per million.
  • Another example of a suitable biostabilizer may be 10.10′-oxybisphenoxarsine (OBPA), examples of which may include VINYZENE™ BP 5-2 Series, VINYZENE™ BP 5-5 Series, VINYZENE™ SB 1, and VINYZENE™ SB 1 Series. The OBPA biostabilizer may be dispersed throughout the crystalline polymer 2, but preferably the amorphous polymer 6, in any concentration suitable to prevent or reduce mold or mildew growth on the composite 1, for example, between about 200 parts per million and about 500 parts per million. The OBPA biostabilizer may have a thermal stability of about 300° C. and/or a solubility in water of about 6 parts per million.
  • A further example of a suitable biostabilizer may be octyl-isothiazoline (OIT), examples of which may include VINYZENE™ IT 3000 Series, VINYZENE™ IT 3010 Series, VINYZENE™ IT 3025 DIDP, and VINYZENE™ SB 8. The OIT biostabilizer may be dispersed throughout the crystalline polymer 2, but preferably the amorphous polymer 6, in any concentration suitable to prevent or reduce mold or mildew growth on the composite 1, for example, between about 800 parts per million and about 1200 parts per million. The OIT biostabilizer may have a thermal stability of about 220° C. and/or a solubility in water of about 500 parts per million.
  • Yet another example of a suitable biostabilizer may be trichlorophenoxyphenol (TCPP), examples of which may include VINYZENE™ SB 30. The TCPP biostabilizer may be dispersed throughout the crystalline polymer 2, but preferably the amorphous polymer 6, in any concentration suitable to prevent or reduce mold or mildew growth on the composite 1, for example, between about 800 parts per million and about 1200 parts per million. The TCPP biostabilizer may have a thermal stability of about 230° C. and/or a solubility in water of about 10 parts per million.
  • A yet further example of a suitable biostabilizer includes biostabilizers that prevent and/or reduce the growth of any of the following exemplary fungi, bacteria, and/or actinomycetes on composite 1: Alternaria, Aureobasidium, Curvularia, Aspergillus, Penicillium, Fusarium, Bigrospora, Chaetomium, Gliocladium, Helminthsporium, and/or all of the subspecies of the aforementioned fungi, bacteria, and/or actinomycetes.
  • Still another example of a suitable biostabilizer (e.g., biocide) includes biostabilizers having one or more of the following features: substantially non-toxic; safe and environmentally friendly; broad spectrum; compatibility with formulation; leach and ultraviolet resistant; has sufficient thermal stability; and ease of use and handling.
  • A still further example of a suitable biostabilizer may include zinc borate, which may be in the form of a crystalline powder having a solubility in water of about 2800 parts per million and a particle sizes between about 1-2 microns.
  • Other examples of suitable biostabilizers (e.g., biocides) and methods for determining suitable biostabilizers for wood-plastic and other composites were disclosed in a presentation entitled Maintaining the Aesthetic Quality of WPC Decking with Isothiazolone Biocide by Peter Dylingowski, which was presented on May 20, 2003 at the 7th International Conference on Wood-Fiber Plastic Composites, the entirety of which is incorporated herein by reference.
  • An exemplary embodiment of the invention includes a method of manufacturing a wood-plastic composite. As shown in FIGS. 4A-4C, the method may include providing a first polymer 2, providing a plurality of wood fibers 3, providing a second polymer 6 configured to resist blending with first polymer 2, melting first polymer 2, melting second polymer 6, mixing second polymer 6 with first polymer 2 and wood fibers 3 to form a feed 10, and forming a profile body 1. Profile body 1 may include an outer surface 5 deliberately evincing a first color and a second color different from the first color. Profile body 1 may also include an outer surface 5 being substantially composed of second polymer 6, with a cross-sectional profile of profile body 1 showing that a layer of second polymer 6 may be substantially disposed around blend 4 of first polymer 2 and wood fibers 3.
  • First polymer 2 may include a crystalline polymer 2. Crystalline polymer 2 is preferably at least one of high density polyethylene (HDPE), low density polyethylene (LDPE), linear low density polyethylene (LLDPE), and polypropylene (PP), however, any crystalline polymer may be used in composite 1, such as one or more polyamides (PA), nylons, polyoxymethylenes, polybutylene terephthalates (PBT), polyethylene terephthalates (PET);.and/or acetals. First polymer 2 may be provided in any suitable form (e.g., pellets, flakes, sheets, etc.) to be melted, mixed with wood fibers 3, and/or extruded into a dimensionally stable profile. First polymer 2 may have any suitable size, shape, and/or configuration to be used in any of the apparatuses or methods disclosed in co-owned U.S. Pat. Nos. 5,851,469 and 6,527,532, co-pending and co-owned U.S. patent application Ser. No. 10/292,672 filed Nov. 12, 2002, and co-pending and co-owned U.S. patent application Ser. No. 10/668,368 filed Sep. 24, 2003, the entirety of all of which are incorporated herein by reference. First polymer 2 may be processed prior to extruding the feed 10 using any suitable method. For example, first polymer 2 may be chopped, purified, shredded, heated, and/or demoistured. In various embodiments, first polymer 2 may be heated (e.g., by shear friction with the apparatus or by the application of external thermal energy) to completely melt, partially melt, and/or improve processability.
  • Crystalline polymers 2 may be selected because they have a specific color (e.g., be mixed with a certain color dye) and/or composition (e.g., allows background color 9 to suitable permeate its structure). However, because crystalline polymers 2 (and/or its additives such as background color 9) tend to blend and form a substantially homogenous color, the specific colors and/or compositions of crystalline polymers 2 used in the process need not be tightly controlled. Some specific dyes may affect the resulting color of profile body 1 more than other dyes. One of ordinary skill in the art may control crystalline polymers 2 input into the process in order to achieve the desired resultant color for outer surface 5. Moreover, the resultant color of crystalline polymers 2 after processing (e.g., heating and/or extrusion) may be different from the initial colors of crystalline polymers 2. Crystalline polymer 2 may have any suitable size, shape, and/or configuration, exemplary parameters for which have already been set forth herein.
  • Second polymer 6 may include an amorphous polymer. Amorphous polymer 6 is preferably a styrenic polymer such as polystrene (PS), however, any amorphous polymer may be used in composite 1, such as one or more of Impact PS, polymethylmethacrylates (PMMA), polyvinyl chlorides (PVC), acrylonitrile-butadine-styrene copolymers (ABS), thermoplastic polyurethanes (TPU), styrene acrylonitrile copolymers (SAN), polyphenyl oxide (PPO), acryla-styrene butyl-acrylate or acrylate styrene acrylonitrile (either of which may be abbreviated as ASA), and/or polycarbonates (PC). Second polymer 6 may be provided in any suitable form (e.g., pellets, flakes, sheets, films, etc.) Second polymer 6 may be processed prior to extruding the feed 10 using any suitable method. For example, second polymer 6 may be chopped, shredded, heated, purified, and/or demoistured. In another example, background color may be added to second polymer 6, and then second polymer 6 may introduced into a processing apparatus, such as extruder 15, substantially cold (e.g., without processing) to be mixed with blend 4 and/or into the processing apparatus as close to the extruder die 19 of the processing apparatus as possible to be extruded with blend 4.
  • Amorphous polymer 6 used may be selected based on its color and/or composition. Amorphous polymer 6 may have an initial color and/or resultant color that is different from the initial color and/or resultant color of the one or more crystalline polymers (with or without wood fibers 3) that amorphous polymer 6 is being mixed with. For example, crystalline polymers 2, after processing (with or without wood fibers 3 and/or background color 9), may result in a substantially gray color, while amorphous polymer 6, after processing, may result in a substantially black color. Amorphous polymer 6 may have any suitable size, shape, and/or configuration. For example, amorphous polymer 6 may be provided in flake or pellet form.
  • Crystalline polymer 2 and/or amorphous polymer 6 may be melted using any suitable method. For example, crystalline polymer 2 and/or amorphous polymer 6 may be heated using in an external heat source (e.g., a flame in a heater 13) or may be heated through kinetic energy (e.g., by passing through a barrel 12 with a rotating screw 11, or passing through extruder die 19). Crystalline polymer 2 and/or amorphous polymer 6 may be melted at any point in the composite manufacturing process prior to forming profile body 1. Crystalline polymer 2 and/or amorphous polymer 6 may be heated separately and/or together. In a preferred embodiment, crystalline polymer 2 and/or wood-fibers 3 may be heated and blended to form blend 4. Crystalline polymer 2 may be heated substantially throughout crystalline polymer 2 and/or enough to improve processability (e.g., mixing and/or blending).
  • Wood fibers 3 may be from any type of suitable wood, for example, one or more hardwoods and/or softwoods. Wood fibers 3 may also be mixed with and/or replaced by any organic or inorganic filler such as those set forth herein. Wood fibers 3 may be of any suitable shape and/or size, and may be configured to be suitably blended with crystalline polymer 2 such that a mixture of wood fibers. 3 and crystalline polymer 2 appears substantially homogenous in color. Wood fibers 3 may be processed prior to forming profile body 1 using any suitable method. For example, wood fibers 3 may be chopped, shredded, heated, purified, and/or demoisturized. Wood fibers 3 may be dried prior to being blended with crystalline polymer 2 to form blend 4. In some cases, pieces of wood fiber 3 may be discernible in blend 4, however, wood fiber 3 will still typically have the same homogenous color as the rest of blend 4.
  • Crystalline polymer 2 may be blended in a processor 13 with wood fibers 3 such that blend 4 is substantially homogenous. For example, blend 4 may have one substantially solid color and/or have a substantially uniform consistency. Blend 4 may be formed using any suitable method. Crystalline polymer 2 and wood fibers 3 may be blended by placing them together either before, during, or after crystalline polymer 2 and/or wood fibers 3 are dried. Crystalline polymer 2 and wood fibers 3 may be blended using applied heat and/or mechanical agitation. Such blending may be accomplished by an extruder, high shear device, and/or a low shear mixer with or without the application of heat.
  • Second polymer 6 may be mixed with first polymer 2 and wood fibers 3 to form a feed 10 in any suitable order, any suitable ratio, and using any suitable method. For example, first polymer 2, second polymer 6, and plurality of wood fibers 3 may be mixed as they are advanced by one or more screws 11 in a barrel 12 and/or extruded through die 19. Second polymer 6 may be mixed with first polymer 2 and wood fibers 3 at any time prior to extruding the feed and in any relative order. For example, first polymer 2 may be blended with wood fibers 3, the blend may be heated, and then second polymer 6 may be added to the blend. In another example, first polymer 2, second polymer 6, and wood fibers 3 may be combined at substantially the same time and mixed simultaneously. Second polymer 6 may be mixed with first polymer 2 and wood fibers 3 such that the mixture does not blend. For example, the mixture may be heated to a temperature that allows mixing but not blending.
  • In another example, second polymer 6 may be added to blend 4 to form feed 10 just prior to extruding feed 10 through extruder die 19. Thus, heating of second polymer 6 may only occur just after introducing second polymer 6 into blend 4 and/or during extrusion of feed 10 through extruder die 19. Accordingly, second polymer 6 may experience less of a heat history than any of first polymer 2, wood fibers 3, and/or blend 4, which may assist in preventing blending.
  • In a further example, the structures (e.g., crystalline structures, lack of crystalline structures, polymer backbones, polarity, compositions, etc.) of first polymer 2 and second polymer 6 may assist in preventing the polymers 2, 6, from substantially blending. Exemplary percentages of first polymer 2, second polymer 6, and wood fibers. 3 are listed herein, however, generally, the percentage of first polymer 2 will exceed the percentage of second polymer 6.
  • In various embodiments, composite 1 may include between about 100% and about 20% of crystalline polymer 2, between about 5% and about 0% of amorphous polymer 6, and between about 0% and about 80% wood fiber or other filler. In a preferred embodiment, composite 1 may include between about 60% and about 53% of crystalline polymer 2, about 2% of amorphous polymer 6, and between about 45% and about 38% wood fiber or other filler
  • Besides having a more natural, smooth, non-monolithic, and/or three-dimensional looking surface, composites 1 discussed herein may have other advantages. For example, composite 1 may be less susceptible to mold and mildew and/or may be more durable. Crystalline polymer 2 and amorphous polymer 6 do not blend in composites 1. Accordingly, the minor component (in this case, amorphous polymer 6) may migrate to the outer surface 5 of composite 1. When the minor component migrates to outer surface 5 of composite 1, the minor component may tend to coat at least portions of outer surface 5 (e.g., top, bottom, and/or side surfaces) with a polymer rich coating that does not absorb moisture, and thus allows outer surface 5 to resist molding and/or mildewing. Moreover, additional additives, such as mold and mildew resistant compounds (e.g., DCOIT biostabilizers or other suitable anti-fungi bacteria materials/compounds, examples of which are set forth herein, or other materials having other desirable properties for composite 1), may be added to amorphous polymer 6 at any point before or during the manufacturing process of composite 1. During the addition of the additive to amorphous polymer 6, the additive and amorphous polymer 6 may be processed so as to substantially disperse the additive through the matrix of amorphous polymer 6. Once again, because amorphous polymer 6 may migrate to outer surface 5 of composite 1, amorphous polymer 6 with mildew resistant additives (or other materials) may coat at least portions of outer surface 5. Some exemplary reasons why amorphous polymer 6 may migrate toward outer surface 5 of composite 1 are set forth herein, and especially below.
  • This type of delivery of the mold and mildew resistant materials and/or compounds, examples of which are set forth herein, (or other compounds with other desirable properties) to specific portions of composite 1 may have many advantages. For example, the compounds themselves may be relatively expensive and/or including too much of the compound in composite 1 may compromise some structural and/or aesthetic properties of composite 1. Thus, there may be a need to minimize the amount of the compound in composite 1 by delivering the compound to portions of the composite 1 where the compound may be most effective. In the case of mildew and/or mold resistant compounds (examples of which are set forth herein), such compounds may be most effective on at least portions of outer surface 5 of composite 1. Accordingly, because the properties (e.g., crystalline structure, solubility, or other properties like or similar to those set forth herein) of first polymer 2 (e.g., crystalline polymer) and second polymer 6 (e.g., amorphous polymer) causes second polymer 6, when extruded, to migrate away from first polymer 2 (e.g., with or without wood fibers 3) and/or toward outer surface 5 of composite 1, second polymer 6 may be used as a vehicle to deliver desirable compounds on and/or toward outer surface 5. In some cases, if the property of the compound is desirable along large portions of outer surface 5, then second polymer 6 with the desirable compound may be disposed along entire portions of outer surface 5, for example, as set forth in FIG. 3C.
  • Profile body 1 with an outer surface 5 may be formed using any suitable method. For example, the mixture including first polymer 2 (e.g., crystalline polymer), second polymer 6 (e.g., amorphous polymer), and wood fibers 3 may be extruded through a die 19 to form profile body 1. Feed 10 may be extruded using either a single screw extruder or a double screw extruder to form profile body 1. Feed 10 may also be formed into profile body 1 using any suitable method.
  • Outer surface 5 of profile body 1 may be variegated. Streaks 16 may be formed on outer surface 5 of profile body 1. For example, if crystalline polymer 2 and amorphous polymer 6 are mixed, the chemical properties of the two polymers and/or the processing conditions (e.g., temperature, extrusion rate, mixing rate that the two polymers are subjected to) may prevent them from blending with each other and forming a homogenous color. Accordingly, “clumps” or “pockets” of amorphous polymer 6 may be dispersed through crystalline polymer 2 and vice versa. As the mixture of amorphous polymer 6 and crystalline polymer 2 (with or without wood fibers 3) is extruded through the die 19, amorphous polymer 6 may tend to go towards outer surface 5 of profile body 1, for example, due the pressures exerted on feed 10 during extrusion. In another example, due to the molecular structure of both crystalline polymer 2 and amorphous polymer 6, the polymer chain of amorphous polymer 6 cannot interlock easily with the polymer chain and/or matrix of crystalline polymer 2. Accordingly, amorphous polymer 6 may tend to separate from the polymer matrix of crystalline polymer 2 and go to outer surface 5 so as to form its own solid polymer matrix of amorphous polymer 6. As amorphous polymer 6 reaches surface 5, because amorphous polymer 6 may have a different initial color and/or different resultant color as the rest of profile body 1 (i.e., blend 4 of crystalline polymer 2 and wood fibers 3), streaks 16 of amorphous polymer 6 may be readily discernible on outer surface 5. Streaks 16 may be generally perpendicular to a cross-section of die 19 through which profile body 1 is extruded. However, streaks 16 may be in any direction, and have any other shape and/or configuration, for example, similar to those set forth in FIGS. 2A-2C.
  • In another example, entire portions of outer surface 5 may be composed of amorphous polymer 6, for example, as shown in FIG. 3C. In such an example, the processing may have been such that amorphous polymer 6 forms “clumps” or “pockets” (e.g., as set forth in the previous paragraph) around substantially all of blend 4 so as to form a substantially solid matrix around blend 4 (e.g., with or without wood fibers 3). Any suitable proportions of amorphous polymer 6, crystalline polymer 2, wood-fibers 3, blend 4, blend 18, background color 9, and another other material or compound set forth herein are contemplated as being discernible on outer surface 5.
  • The method may also include providing another amorphous polymer 7, melting another amorphous polymer 7, and mixing another amorphous polymer 7 with amorphous polymer 6, crystalline polymer 2, and/or wood fibers 3. With the addition of additional amorphous polymer 7, the step of extruding may include forming profile body 1 such that outer surface 5 deliberately evinces a third color different from the first color and the second color due to additional amorphous polymer 7.
  • Another amorphous polymer 7 may be selected because its initial color and/or resultant color may be different from an initial color and/or resultant color of one or more of crystalline polymer 2 and/or wood fibers 3. Another amorphous polymer 7 may processed and/or behave similarly to other amorphous polymers 6, thus, streaks 16B of another amorphous polymer 7 may be formed on outer surface 5 of profile body 1. Streaks 16B from another amorphous polymer 7 may be of a color different from either the base color of profile body 1 and/or the color of streaks 16A from amorphous polymer 6.
  • As shown in FIG. 4B, the method may also include providing a core 8 and forming profile body 1 around at least a portion of core 8. Core 8 may be a wood-plastic composite or any other suitable composite. Core 8 may have a cross-sectional area smaller than a cross-sectional area of die 19. Core 8 may be fed by extruder 15 through die 19 such that core 8 advances through substantially the center of die 19 without contacting any portion of die 19 itself. Extruder 15 and/or die 19 may then deposit an outer surface 5 on core 8 that has more than one color (e.g., variegated and/or streaked) using one or more of the methods set forth herein. The variegated surface 5 may be bonded to core 8 using any suitable method, for example, when variegated surface 5 is co-extruded onto core 8, a portion of core 8 may melt and intermix with variegated surface 5 such that core 8 and the variegated surface 5 are substantially fused. Accordingly, the resultant product may be a building material with a core 8 having a wood-plastic composite having a deliberately variegated outer surface 5 formed around it. Such a resultant product may be desirable, for example, to impart strength to the component (e.g., by providing a core component having a high strength such as aluminum or steel).
  • The method also may include the use of a background color 9. As shown in FIG. 4B, background color 9 may be added to crystalline polymer 2 and/or wood fiber 3 (e.g., blend 4) to impart a color to blend 4 different from an initial color of blend 4, crystalline polymer 2, and/or wood fiber 3. Background color 9, crystalline polymer 2, wood fibers 3, and/or blend 4 may be processed by processor 13 using any suitable apparatus and/or method to form resultant blend 4. Resultant blend 4 may then be transferred to extruder 15 and processed with amorphous polymer 6 to form profile body 1 with streaks 16 or other variations of outer surface 5 as set forth herein. Background color 9 may be added to any step of the process and/or any component or subcomponent of the process at any time prior to extrusion through die 19.
  • In a preferred embodiment, as shown in FIG. 4C, background color 9 may be added to amorphous polymer 6 to impart a color to amorphous polymer 6 different from an initial color of amorphous polymer 6. Background color 9 and/or amorphous polymer 6 may be processed by processor 17 using any suitable apparatus and/or method to form resultant blend 18 of amorphous polymer 6 and background color 9. Resultant blend 18 may then be transferred to extruder 15 and processed with crystalline polymer 2, wood fibers 3, and/or blend 4 to form profile body 1 with streaks 16 or other variations of outer surface 5 as set forth herein. Once again, background color 9 may be added to any step of the process and/or any component or subcomponent of the process at any time prior to extrusion through die 19.
  • One of ordinary skill in the art will recognize that some aspects of the invention may be multiplied so as to form different embodiments of the invention. For example, there may be a plurality of crystalline polymers, a plurality of types of wood fibers, and/or a plurality of amorphous polymers used.
  • One of ordinary skill of art will further recognize that some of the aspects of set forth herein may be combined with other aspects set forth herein to form different embodiments of the invention. For example, composite 1 with streaks having multiple colors may also include a core.
  • One of ordinary skill in the art will also recognize that some of the aspects set forth herein may be removed to form different embodiments of the invention. For example, crystalline polymer 2 and wood fibers need not be blended prior to mixing them with amorphous polymer 6.
  • Other embodiments of the invention will be apparent to those skilled in the art from consideration of the specification and practice of the invention disclosed herein. It is intended that the specification and examples be considered as exemplary only, with a true scope and spirit of the invention being indicated by the following claims.

Claims (50)

1-10. (canceled)
11. A composite, comprising:
a first polymer;
a plurality of wood fibers blended with the first polymer to form a substantially homogenous blend;
an outer surface of the composite; and
a second polymer substantially immiscible with the first polymer;
wherein the composite includes an substantially immiscible mixture of the substantially homogenous blend and the second polymer;
wherein the outer surface of the composite is defined by the substantially immiscible mixture of the substantially homogenous blend and the second polymer;
wherein the substantially homogenous blend of the first polymer and the plurality of wood fibers has a first color and the second polymer has a second color different from the first color,
wherein the first color and the second color are separately discernible on the other outer surface.
12. The composite of claim 11, wherein the first polymer is at least one of polypropylene and polyethylene.
13. The composite of claim 11, wherein the second polymer is a styrenic polymer.
14. The composite of claim 11, wherein the outer surface includes streaks of the second color.
15. The composite of claim 11, wherein the first polymer has a melting temperature that is substantially the same as a melting temperature of the second polymer.
16. The composite of claim 11, wherein the outer surface of the composite is variegated by the first color and the second color.
17. The composite of claim 11, wherein a first portion of the outer surface has the first color and a second portion of the outer surface has the second color.
18. The composite of claim 11, further comprising a third polymer substantially immiscible with the first polymer;
wherein the third polymer is visible on the outer surface of the composite,
wherein the third polymer has a third color different from the first color and the second color,
wherein the composite includes an substantially immiscible mixture of the substantially homogenous blend, the second polymer, and the third polymer;
wherein the outer surface of the composite is defined by the substantially immiscible mixture of the substantially homogenous blend, the second polymer, and the third polymer.
19. The composite of claim 11, wherein the composite is at least one of a building material, a decking material, a railing component, and a decking board.
20. The composite of claim 11, further comprising a colorant blended with one of the first polymer and the second polymer.
21-45. (canceled)
46. The composite of claim 11, wherein the plurality of wood fibers are substantially free of the second polymer.
47. The composite of claim 11, wherein the second polymer of the composite is substantially free of the plurality of wood fibers.
48. The composite of claim 11, wherein at least one of the substantially homogenous blend and the second polymer is miscibly blended with at least one of a biostabilizer and a biocide.
49. The composite of claim 11, wherein the second polymer makes up between about 5% and about 0% of the composite by weight.
50. The composite of claim 11, wherein the second polymer makes up about 2% of the composite by weight.
51. A composite, comprising:
a substantially homogenous blend including a first polymer and a plurality of wood fibers; and
an substantially immiscible mixture of the substantially homogenous blend and a second polymer,
wherein the substantially homogenous blend is of a first color and the second polymer is of a second color different from the first color, and
wherein the composite includes a variegation of the first color and the second color.
52. The composite of claim 51, wherein the first polymer is at least one of polypropylene and polyethylene.
53. The composite of claim 51, wherein the second polymer is a styrenic polymer.
54. The composite of claim 51, further comprising an outer surface defined by the substantially immiscible mixture including the substantially homogenous blend and the second polymer.
55. The composite of claim 54, wherein the outer surface includes streaks of the second color.
56. The composite of claim 51, wherein the second polymer has a melting temperature that is substantially the same as a melting temperature of the first polymer.
57. The composite of claim 54, wherein the outer surface of the composite is variegated by the first color and the second color.
58. The composite of claim 54, wherein a first portion of the outer surface has the first color and a second portion of the outer surface has the second color.
59. The composite of claim 51, wherein the substantially immiscible mixture includes another second polymer different from the second polymer,
wherein the another second polymer is substantially immiscible with the substantially homogenous blend, and
wherein the another second polymer has a third color different from the first color and the second color.
60. The composite of claim 51, wherein the composite is at least one of a building material, a decking material, a railing component, and a decking board.
61. The composite of claim 51, further comprising a colorant blended with one of the first polymer and the second polymer,
wherein the colorant has a color different from a color of the one of the first polymer and second polymer, and
wherein a substantially homogenous blend of the colorant and the one of the first polymer and second polymer has the color of the colorant.
62. The composite of claim 51, wherein the plurality of wood fibers are substantially free of the second polymer.
63. The composite of claim 51, wherein the second polymer of the composite is substantially free of the plurality of wood fibers.
64. The composite of claim 51, wherein at least one of the substantially homogenous blend and the second polymer is miscibly blended with at least one of a biostabilizer and a biocide.
65. The composite of claim 51, wherein the second polymer makes up between about 5% and about 0% of the composite by weight.
66. The composite of claim 51, wherein the second polymer makes up about 2% of the composite by weight.
67. A composite, comprising:
an substantially immiscible mixture of a first polymer and a second polymer; and
a plurality of wood fibers dispersed throughout the first polymer,
wherein the first polymer is of a first color and the second polymer is of a second color different from the first color, and
wherein the second polymer is substantially free of the plurality of wood fibers.
68. The composite of claim 67, wherein the first polymer is at least one of polypropylene and polyethylene.
69. The composite of claim 67, wherein the second polymer is a styrenic polymer.
70. The composite of claim 67, further comprising an outer surface defined by the substantially immiscible mixture of the first polymer and the second polymer.
71. The composite of claim 70, wherein the outer surface includes streaks of the second color.
72. The composite of claim 67, wherein the second polymer has a melting temperature that is substantially the same as a melting temperature of the first polymer.
73. The composite of claim 70, wherein the outer surface of the composite is variegated.
74. The composite of claim 70, wherein a first portion of the outer surface has the first color and a second portion of the outer surface has the second color.
75. The composite of claim 67, wherein the substantially immiscible mixture includes another second polymer different from the second polymer,
wherein the another second polymer is substantially immiscible with the first polymer, and
wherein the another second polymer has a third color different from the first color and the second color.
76. The composite of claim 67, wherein the composite is at least one of a building material, a decking material, a railing component, and a decking board.
77. The composite of claim 67, further comprising a colorant blended with one of the first polymer and the second polymer,
wherein the colorant has a color different from a color of the one of the first polymer and second polymer,
wherein a substantially homogenous blend of the colorant and the one of the first polymer and second polymer has the color of the colorant.
78. The composite of claim 67, wherein at least one of the first polymer and the second polymer is miscibly blended with at least one of a biostabilizer and a biocide.
79. The composite of claim 67, wherein the second polymer makes up between about 5% and about 0% of the composite by weight.
80. The composite of claim 67, wherein the second polymer makes up about 2% of the composite by weight.
81. The composite of claim 13, wherein the second polymer is one of a polycarbonate and a polystyrene.
82. The composite of claim 53, wherein the second polymer is one of a polycarbonate and a polystyrene.
83. The composite of claim 69, wherein the second polymer is one of a polycarbonate and a polystyrene.
US11/544,567 2004-06-08 2006-10-10 Variegated composites and related methods of manufacture Abandoned US20070087181A1 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
US11/544,567 US20070087181A1 (en) 2004-06-08 2006-10-10 Variegated composites and related methods of manufacture

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US10/862,448 US7410687B2 (en) 2004-06-08 2004-06-08 Variegated composites and related methods of manufacture
US11/544,567 US20070087181A1 (en) 2004-06-08 2006-10-10 Variegated composites and related methods of manufacture

Related Parent Applications (1)

Application Number Title Priority Date Filing Date
US10/862,448 Division US7410687B2 (en) 2004-06-08 2004-06-08 Variegated composites and related methods of manufacture

Publications (1)

Publication Number Publication Date
US20070087181A1 true US20070087181A1 (en) 2007-04-19

Family

ID=35449313

Family Applications (4)

Application Number Title Priority Date Filing Date
US10/862,448 Expired - Fee Related US7410687B2 (en) 2004-06-08 2004-06-08 Variegated composites and related methods of manufacture
US11/094,795 Abandoned US20060068215A2 (en) 2004-06-08 2005-03-31 Improved variegated composites and related methods of manufacture
US11/544,566 Abandoned US20070087180A1 (en) 2004-06-08 2006-10-10 Variegated composites and related methods of manufacture
US11/544,567 Abandoned US20070087181A1 (en) 2004-06-08 2006-10-10 Variegated composites and related methods of manufacture

Family Applications Before (3)

Application Number Title Priority Date Filing Date
US10/862,448 Expired - Fee Related US7410687B2 (en) 2004-06-08 2004-06-08 Variegated composites and related methods of manufacture
US11/094,795 Abandoned US20060068215A2 (en) 2004-06-08 2005-03-31 Improved variegated composites and related methods of manufacture
US11/544,566 Abandoned US20070087180A1 (en) 2004-06-08 2006-10-10 Variegated composites and related methods of manufacture

Country Status (2)

Country Link
US (4) US7410687B2 (en)
MX (1) MXPA06014301A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20080093763A1 (en) * 2006-10-06 2008-04-24 Douglas Mancosh Multi-color fiber-plastic composites and systems and methods for their fabrication

Families Citing this family (45)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20080010924A1 (en) 2006-07-12 2008-01-17 Pietruczynik Christopher B Exterior building material having a hollow thin wall profile and an embossed low gloss surface
US7258913B2 (en) * 2002-10-28 2007-08-21 Certainteed Corp. Plastic fencing system reinforced with fiberglass reinforced thermoplastic composites
US20050255305A1 (en) * 2001-11-19 2005-11-17 Jo Byong H Thermoplastic composite building product having continuous fiber reinforcement
US20030096096A1 (en) * 2001-11-19 2003-05-22 Jo Byeong H. Plastic rail system reinforced with fiberglass thermoplastic composites
US20070235705A1 (en) * 2003-02-27 2007-10-11 Crane Plastics Company Llc Composite fence
JP4343223B2 (en) * 2004-04-15 2009-10-14 ポリプラスチックス株式会社 Method for producing resin composition pellets with controlled length of fibrous filler
US20060068053A1 (en) * 2004-09-30 2006-03-30 Crane Plastics Company Llc Integrated belt puller and three-dimensional forming machine
US20060100466A1 (en) 2004-11-08 2006-05-11 Holmes Steven A Cycloalkane base oils, cycloalkane-base dielectric liquids made using cycloalkane base oils, and methods of making same
US7473722B2 (en) * 2004-11-08 2009-01-06 Certain Teed Corp. Polymer-fiber composite building material with bulk and aesthetically functional fillers
US8074339B1 (en) 2004-11-22 2011-12-13 The Crane Group Companies Limited Methods of manufacturing a lattice having a distressed appearance
US7111408B2 (en) * 2005-02-02 2006-09-26 Cooper Brands, Inc. Folding rule
CA2609517A1 (en) * 2005-05-22 2006-11-30 U.S. Borax Inc. Co-biocidal formulation for polymeric materials
US8167275B1 (en) 2005-11-30 2012-05-01 The Crane Group Companies Limited Rail system and method for assembly
US7875655B2 (en) 2006-01-20 2011-01-25 Material Innovations, Llc Carpet waste composite
US7743567B1 (en) 2006-01-20 2010-06-29 The Crane Group Companies Limited Fiberglass/cellulosic composite and method for molding
DE102006018277B4 (en) * 2006-04-20 2008-04-17 Kronotec Ag Building board and method for producing a building board
CN101657308B (en) * 2006-11-22 2013-06-19 材料革新公司 Plastic composites using recycled carpet waste and systems and methods of recycling carpet waste
US8460797B1 (en) 2006-12-29 2013-06-11 Timbertech Limited Capped component and method for forming
US20080172981A1 (en) * 2007-01-22 2008-07-24 Crawford Industries Llc Non-organic composite lumber
US7913960B1 (en) 2007-08-22 2011-03-29 The Crane Group Companies Limited Bracketing system
US8431242B2 (en) 2007-10-26 2013-04-30 Global Oled Technology, Llc. OLED device with certain fluoranthene host
US8420229B2 (en) * 2007-10-26 2013-04-16 Global OLED Technologies LLC OLED device with certain fluoranthene light-emitting dopants
US8076009B2 (en) 2007-10-26 2011-12-13 Global Oled Technology, Llc. OLED device with fluoranthene electron transport materials
US20090258208A1 (en) * 2008-04-10 2009-10-15 Martin Brad J Compositions And Composite Articles Suitable For High Heat Applications
WO2009152026A1 (en) * 2008-06-10 2009-12-17 Dow Global Technologies Inc. Surface color patterning while drawing polymer articles
US7931975B2 (en) 2008-11-07 2011-04-26 Global Oled Technology Llc Electroluminescent device containing a flouranthene compound
US8088500B2 (en) 2008-11-12 2012-01-03 Global Oled Technology Llc OLED device with fluoranthene electron injection materials
US7968215B2 (en) 2008-12-09 2011-06-28 Global Oled Technology Llc OLED device with cyclobutene electron injection materials
KR20110123240A (en) 2008-12-19 2011-11-14 파이버 콤포지트 엘엘씨. Wood-plastic composites utilizing ionomer capstocks and methods of manufacture
EP2547505A1 (en) * 2010-03-16 2013-01-23 Andersen Corporation Sustainable compositions, related methods, and members formed therefrom
KR101379544B1 (en) 2011-06-17 2014-03-28 (주)엘지하우시스 Window profile provided with skin layer having wood fiber
WO2013123364A1 (en) 2012-02-17 2013-08-22 Andersen Corporation Polylactic acid containing building component
US9023455B2 (en) * 2013-01-30 2015-05-05 Ford Global Technologies, Llc Method of making reinforced composite articles with reduced fiber content in local areas and articles made by the method
US8826510B1 (en) 2013-02-15 2014-09-09 Ford Global Technologies, Llc Method of making assemblies including reinforced composite parts with pre-formed rivet receiving buttons and articles made by the method
CN103642121A (en) * 2013-11-01 2014-03-19 界首市天翔塑料制品有限公司 Hot-pressing wood plastic composite material for toy
US20160075866A1 (en) 2014-09-12 2016-03-17 Teknor Apex Company Compositions for capstock applications
US10981350B1 (en) 2015-08-24 2021-04-20 Tangent Technologies Llc Wood-grained polymer substrate
USD819234S1 (en) 2016-08-24 2018-05-29 Tangent Technologies Llc Wood-grained polymer board
USD819236S1 (en) 2016-08-24 2018-05-29 Tangent Technologies Llc Wood-grained polymer board
USD819235S1 (en) 2016-08-24 2018-05-29 Tangent Technologies Llc Wood-grained polymer board
USD827869S1 (en) 2016-08-24 2018-09-04 Tangent Technologies Llc Wood-grained polymer board
CN111703155A (en) * 2020-04-28 2020-09-25 安徽昊森新材料科技有限公司 Wood-plastic composite material and preparation method thereof
JP7437106B2 (en) * 2020-06-25 2024-02-22 トヨタ車体株式会社 Method for producing fiber reinforced resin composition
US11572646B2 (en) 2020-11-18 2023-02-07 Material Innovations Llc Composite building materials and methods of manufacture
WO2023038856A1 (en) 2021-09-08 2023-03-16 Greentech Composites Llc Non-polar thermoplastic composite having a dye sublimation printed image and method to form them

Citations (93)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US1700208A (en) * 1926-11-19 1929-01-29 Paisseau Jean Process and apparatus for production of a substance having a nacreous and chatoyant aspect
US2067012A (en) * 1933-10-09 1937-01-05 Emil C Loetscher Composite building material
US2149066A (en) * 1936-12-09 1939-02-28 Nixon Nitration Works Method for obtaining luster, color, pattern, and complicated shape effects
US2702408A (en) * 1950-07-27 1955-02-22 Union Carbide & Carbon Corp Extrusion of thermoplastic materials
US2736064A (en) * 1956-02-28 rubin
US2744013A (en) * 1952-05-09 1956-05-01 Rodger M Dorland Artificial board
US2832993A (en) * 1952-05-13 1958-05-06 Western Electric Co Apparatus for extruding and cooling plastics
US3023136A (en) * 1956-12-17 1962-02-27 Himmelbeber Max Chipwood articles of high compressive strength and processes for producing the same
US3243327A (en) * 1961-05-16 1966-03-29 Hoppeler Walter Method of making a pressed plate
US3651187A (en) * 1969-10-16 1972-03-21 Hercules Inc Extrusion process
US3798294A (en) * 1972-02-10 1974-03-19 Grace W R & Co Method for producing battery separator sheet
US3875088A (en) * 1971-07-16 1975-04-01 Hasbro Industries Inc Pencil sheath compositions
US4003866A (en) * 1974-01-22 1977-01-18 Etablissements Paturle S.A. Construction material and a process for producing the same
US4008858A (en) * 1972-05-12 1977-02-22 Mitsubishi Petrochemical Company Limited Treating device for synthetic resin waste
US4011292A (en) * 1974-04-04 1977-03-08 Rowland, Incorporated Method for producing sheet material with multicolor striated pattern and sheet material produced thereby
US4013616A (en) * 1971-11-22 1977-03-22 Wallace Richard A Mixed polymeric structural material and method
US4018722A (en) * 1975-03-10 1977-04-19 Elizabeth I. Bellack Reclaimed plastic material
US4138534A (en) * 1977-02-07 1979-02-06 Lifetime Foam Products, Inc. Production of structural members from reclaimed polyolefins
US4150185A (en) * 1974-11-05 1979-04-17 Joachim Zur Verth Building materials in the form of woodstone panels or sheets and processes for their production
US4187352A (en) * 1977-04-19 1980-02-05 Lankhorst Touwfabrieken B.V. Method and apparatus for producing synthetic plastics products, and product produced thereby
US4250222A (en) * 1974-12-31 1981-02-10 Institut National De Recherche Chimique Appliquee Process for manufacturing finished and semi-finished products from mixtures of various synthetic resin scrap materials
US4260573A (en) * 1980-02-07 1981-04-07 Kenneth Overman Method for pelletizing wood particulate matter
US4323625A (en) * 1980-06-13 1982-04-06 Monsanto Company Composites of grafted olefin polymers and cellulose fibers
US4326854A (en) * 1979-03-09 1982-04-27 Tanner John D Synthetic firelog
US4376144A (en) * 1981-04-08 1983-03-08 Monsanto Company Treated fibers and bonded composites of cellulose fibers in vinyl chloride polymer characterized by an isocyanate bonding agent
US4379525A (en) * 1981-08-06 1983-04-12 Owens-Illinois, Inc. Process for recycling plastic container scrap
US4510278A (en) * 1981-04-07 1985-04-09 Methanol Chemie Nederland V.O.F. Manufacture of chipboard and a novel suitable bonding agent
US4656722A (en) * 1983-07-25 1987-04-14 Larry Armstrong Method of forming a decorative panel of molded plastic
US4717742A (en) * 1985-05-29 1988-01-05 Beshay Alphons D Reinforced polymer composites with wood fibers grafted with silanes - grafting of celluloses or lignocelluloses with silanes to reinforce the polymer composites
US4738808A (en) * 1985-11-18 1988-04-19 Hammer Floyd V Method of forming articles from a plastic material
US4797242A (en) * 1983-03-29 1989-01-10 Mitsui Toatsu Chemicals, Incorporated Method for shaping thermosetting resins
US4812368A (en) * 1987-01-07 1989-03-14 Basf Aktiengesellschaft Process for the preparation of lightweight, planar molded articles
US4822826A (en) * 1986-09-04 1989-04-18 La Cellulose Du Pin Composite material and method of manufacturing same
US4824627A (en) * 1985-11-18 1989-04-25 Floyd V. Hammer Method of making a molded plastic product
US4913863A (en) * 1989-01-30 1990-04-03 Hoechst Celanese Corporation Split extrusion die assembly for thermoplastic materials and methods of using the same
US4915764A (en) * 1987-05-23 1990-04-10 Mario Miani Method of making panels
US4999390A (en) * 1987-02-16 1991-03-12 Novopan Traeindustri A/S Composite board and a method and a composition for its production
US5082605A (en) * 1990-03-14 1992-01-21 Advanced Environmental Recycling Technologies, Inc. Method for making composite material
US5084135A (en) * 1990-03-27 1992-01-28 Advanced Environmental Recycling Technologies, Inc. Recycling plastic coated paper product waste
US5088910A (en) * 1990-03-14 1992-02-18 Advanced Environmental Recycling Technologies, Inc. System for making synthetic wood products from recycled materials
US5096046A (en) * 1990-03-14 1992-03-17 Advanced Environmental Recycling Technologies, Inc. System and process for making synthetic wood products from recycled materials
US5096406A (en) * 1990-03-14 1992-03-17 Advanced Environmental Recycling Technologies, Inc. Extruder assembly for composite materials
US5277758A (en) * 1990-03-27 1994-01-11 Advanced Environmental Recycling Technologies, Inc. Method for recycling plastic coated paper product waste and polymeric film
US5387381A (en) * 1989-12-07 1995-02-07 Alcan Aluminum Corporation Method for extruding plastic with accent color pattern
US5406768A (en) * 1992-09-01 1995-04-18 Andersen Corporation Advanced polymer and wood fiber composite structural component
US5480602A (en) * 1994-06-17 1996-01-02 Nagaich; Laxmi Extruded particle board
US5486553A (en) * 1992-08-31 1996-01-23 Andersen Corporation Advanced polymer/wood composite structural member
US5502088A (en) * 1991-12-18 1996-03-26 Hododi; Andrei Wood substitute based on lignocellulosic and inorganic materials, method for obtaining the same and use
US5603883A (en) * 1995-04-19 1997-02-18 Lenzing Aktiengesellschaft Process of and apparatus for making celluose products
US5620642A (en) * 1993-03-05 1997-04-15 Misawa Homes Co., Ltd. Simulated wood product manufacturing method and simulated wood product
US5624620A (en) * 1995-05-03 1997-04-29 Turner; James E. Process for making non-extruded molded boards and sheet products
US5725939A (en) * 1994-02-10 1998-03-10 Ein Engineering Co., Ltd. Synthetic wood meal, method and apparatus for manufacturing the same; synthetic wood board including the synthetic wood meal, method and apparatus of extrusion molding therefor
US5866264A (en) * 1996-10-22 1999-02-02 Crane Plastics Company Limited Partnership Renewable surface for extruded synthetic wood material
US5869176A (en) * 1996-04-03 1999-02-09 M. A. Hannacolor, A Division Of M. A. Hanna Company Composition and method for extruding plastic articles having accent color pattern and comprising poly-α-methylstyrene pellets
US5882564A (en) * 1996-06-24 1999-03-16 Andersen Corporation Resin and wood fiber composite profile extrusion method
US6011091A (en) * 1996-02-01 2000-01-04 Crane Plastics Company Limited Partnership Vinyl based cellulose reinforced composite
US6015612A (en) * 1992-08-31 2000-01-18 Andersen Corporation Polymer wood composite
US6015611A (en) * 1992-08-31 2000-01-18 Andersen Corporation Advanced polymer wood composite
US6035588A (en) * 1996-11-21 2000-03-14 Crane Plastics Company Limited Partnership Deck plank
US6054207A (en) * 1998-01-21 2000-04-25 Andersen Corporation Foamed thermoplastic polymer and wood fiber profile and member
US6180257B1 (en) * 1996-10-29 2001-01-30 Crane Plastics Company Limited Partnership Compression molding of synthetic wood material
US6207729B1 (en) * 1997-10-31 2001-03-27 Xyleco, Inc. Texturized cellulosic and lignocellulosic materials and compositions and composites made therefrom
US6210792B1 (en) * 1992-08-31 2001-04-03 Andersen Corporation Advanced compatible polymer wood fiber composite
US6337138B1 (en) * 1998-12-28 2002-01-08 Crane Plastics Company Limited Partnership Cellulosic, inorganic-filled plastic composite
US20020005602A1 (en) * 1998-07-20 2002-01-17 Jacobsen William W. Lignocellulose fiber filler for thermoplastic composite compositions
US6344509B1 (en) * 1994-12-22 2002-02-05 Taiyo Kagaku Co., Ltd. Thermoplastic resin compositions
US6344268B1 (en) * 1998-04-03 2002-02-05 Certainteed Corporation Foamed polymer-fiber composite
US6344504B1 (en) * 1996-10-31 2002-02-05 Crane Plastics Company Limited Partnership Extrusion of synthetic wood material
US6357197B1 (en) * 1997-02-05 2002-03-19 Andersen Corporation Polymer covered advanced polymer/wood composite structural member
US20020033563A1 (en) * 1998-11-12 2002-03-21 Certainteed Corporation. Apparatus for continuous forming shaped polymeric articles
US6376582B1 (en) * 1999-03-29 2002-04-23 Yamaha Corporation Wood fiberboard and manufacturing method therefor
US20020049266A1 (en) * 2000-08-22 2002-04-25 Ajinomoto Co., Inc. Woody thermoplastic resin composition
US6379815B1 (en) * 1997-10-20 2002-04-30 Syntech Holdings B.V. Moulded element, in particular in the shape of a plate, which is a compressed mixture of binder and filler, a method and a device for manufacturing such a moulded elements, as well as floor plates, a sports hall provided with such floor
US20030004232A1 (en) * 2001-06-28 2003-01-02 Certainteed Corporation Non-staining polymer composite product
US20030021915A1 (en) * 2001-06-15 2003-01-30 Vivek Rohatgi Cellulose - polymer composites and related manufacturing methods
US20030025233A1 (en) * 1997-09-05 2003-02-06 Crane Plastics Company Llc In-line compounding and extrusion system
US20030030176A1 (en) * 2001-07-13 2003-02-13 Monovoukas Yiannis A. Cellulose-reinforced thermoplastic composite and methods of making same
US20030032702A1 (en) * 1997-09-02 2003-02-13 Marshall Medoff Compositions and composites of cellulosic and lignocellulosic materials and resins, and methods of making the same
US20030036589A1 (en) * 2000-04-26 2003-02-20 Archuletta Phil T. Method for making wood and plastic composite material
US6526712B2 (en) * 2001-05-21 2003-03-04 Advanced Environmental Recycling Technologies, Inc. Extruded composite interlocking corner assembly
US6531010B2 (en) * 1997-03-28 2003-03-11 Andersen Corporation Thermoplastic resin and fiberglass fabric composite and method
US20030071389A1 (en) * 2000-05-14 2003-04-17 Manning Mark J. Lignocellulosic composites
US6680090B2 (en) * 1999-04-16 2004-01-20 Andersen Corporation Polyolefin wood fiber composite
US6682814B2 (en) * 1997-05-30 2004-01-27 Andersen Corporation Fiber-polymeric composite siding unit and method of manufacture
US6695874B2 (en) * 1998-08-24 2004-02-24 Radiant Medical, Inc. Method and system for control of a patient's body temperature by way of transluminally insertable heat exchange catheter
US20040038002A1 (en) * 2002-08-21 2004-02-26 Sandro Franco Extruded wood imitation component and process
US6708504B2 (en) * 2001-01-19 2004-03-23 Crane Plastics Company Llc Cooling of extruded and compression molded materials
USD488243S1 (en) * 2001-07-06 2004-04-06 Andersen Corporation Door sill portion
US6718704B2 (en) * 2000-11-01 2004-04-13 Andersen Corporation Attachment system for a decorative member
US6722082B1 (en) * 2000-06-28 2004-04-20 Andersen Corporation Window having a hinged weatherstrip
US6726464B1 (en) * 1997-12-04 2004-04-27 Misawa Homes Co. Mixing device for manufacturing molding
US6865849B1 (en) * 2002-01-24 2005-03-15 Crane Plastics Company Llc Top course molding
US6984676B1 (en) * 1996-10-22 2006-01-10 Crane Plastics Company Llc Extrusion of synthetic wood material

Family Cites Families (76)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US942852A (en) 1907-07-13 1909-12-07 Leo H Baekeland Indurated product and method of preparing same.
US1981848A (en) * 1932-08-04 1934-11-27 Walter J Sugden Refrigerating machine
US2332829A (en) * 1939-10-04 1943-10-26 American Plastics Corp Process of making casein plastic products and apparatus therefor
US2617148A (en) 1950-09-07 1952-11-11 Redding Mfg Company Inc Means for forming filamentary articles
US2682031A (en) * 1952-03-11 1954-06-22 Edison Swan Electric Co Ltd Voltage stabilizer circuits
US2759222A (en) 1952-05-07 1956-08-21 Mathew F Kritchever Manufacture of fiber board by extrusion
US3095608A (en) 1959-12-09 1963-07-02 Cabot Corp Process and apparatus for extruding and curing polymeric compositions
US3210451A (en) 1960-12-01 1965-10-05 Celanese Corp Spinnerettes
US3096297A (en) 1961-03-15 1963-07-02 Sun Oil Co Artificial board and process for preparing same
US3328501A (en) * 1962-07-02 1967-06-27 Johns Manville Extrusion process for orienting fibers in molding material
US3222719A (en) 1962-07-27 1965-12-14 Phillips Petroleum Co Extrusion apparatus
US3360462A (en) 1963-09-23 1967-12-26 Mobil Oil Corp Thermosetting resin-thermal asphalt binder composition and fiber board produced therefrom
US3511750A (en) * 1965-10-20 1970-05-12 Owens Illinois Inc Laminates including pulp-thermoplastic boards
US3461496A (en) 1965-11-08 1969-08-19 Thomas W Winstead Apparatus for extruding a skin covered,foamed thermoplastic
US3478138A (en) * 1966-12-01 1969-11-11 Charles E Friesner Method of making thermoplastic articles having non-planar surface contours
US3671615A (en) * 1970-11-10 1972-06-20 Reynolds Metals Co Method of making a composite board product from scrap materials
DE2105998C3 (en) * 1971-02-09 1979-02-15 Furnier- Und Sperrholzwerk J.F. Werz Jr. Kg Werzalit-Pressholzwerk, 7141 Oberstenfeld Device for the production of molded parts from a mixture of lignocellulose-containing fibers and a thermosetting binder
US3769380A (en) * 1971-05-03 1973-10-30 Cosden Oil & Chem Co Method for extruding synthetic thermoplastic sheet material having a variegated colored pattern
DE2148773B2 (en) 1971-09-30 1975-07-31 W.C. Heraeus Gmbh, 6450 Hanau Spinneret plate for spinning organic polymers
JPS55211B2 (en) * 1972-03-23 1980-01-07
JPS5654335B2 (en) * 1972-07-11 1981-12-24
US4154893A (en) * 1972-09-15 1979-05-15 Conrad Goldman Production of thermoplastic billets and preforms
US3890077A (en) * 1973-01-05 1975-06-17 John A Holman Apparatus for manufacturing artificial boards and shapes
CH570869A5 (en) 1973-03-23 1976-05-14 Icma San Giorgio S R L Ind Cos
US4050978A (en) * 1973-05-14 1977-09-27 Moore Alvin E Method for producing light-weight construction member
SE403067B (en) * 1973-07-30 1978-07-31 Svensk Hardbetongteknik Ab FORM FOR THE MANUFACTURE OF PLASTIC MASS PRODUCTS, INCLUDED IN HIGH DEGREE ADDED WITH FINE-DISTRIBUTED FILLING MATERIAL, PREFERABLY WOOD MATERIAL
US3908902A (en) * 1973-10-26 1975-09-30 Collins Synthetics Inc Molded or extruded synthetic railroad ties, beams and structural members
JPS5087439A (en) 1973-12-07 1975-07-14
US4056591A (en) * 1973-12-26 1977-11-01 Monsanto Company Process for controlling orientation of discontinuous fiber in a fiber-reinforced product formed by extrusion
US3927235A (en) * 1974-03-18 1975-12-16 Poo Chow Reconstituted board products from plant-fiber residues
US3956541A (en) * 1974-05-02 1976-05-11 Capital Wire & Cable, Division Of U. S. Industries Structural member of particulate material and method of making same
US4028448A (en) * 1974-11-21 1977-06-07 The Furukawa Electric Co., Ltd. Method of molding plastics material
US4065413A (en) 1975-10-08 1977-12-27 Gte Sylvania Incorporated Fire resistance wood-based boards, process for producing same and compositions useful therefor
US4045603A (en) * 1975-10-28 1977-08-30 Nora S. Smith Construction material of recycled waste thermoplastic synthetic resin and cellulose fibers
DE2610721C3 (en) * 1976-03-13 1978-12-21 Rehau-Plastiks Gmbh, 8673 Rehau Use of a plastic-wood flour mixture for the production of insulation material for the electrical industry
US4100328A (en) 1976-06-04 1978-07-11 Basf Wyandotte Corporation Binder composition and process for preparing pressure molded cellulosic articles
DE2657808C2 (en) * 1976-12-21 1984-05-30 Basf Ag, 6700 Ludwigshafen Low-shrinkage curable polyester molding compositions and process for their production
US4225649A (en) 1978-09-27 1980-09-30 The Flamemaster Corporation Fire retardant composition and cables coated therewith
FI70385C (en) 1978-04-28 1991-08-27 Casco Ab SAETT ATT FRAMSTAELLA CELLULOSABASERADE SKIVMATERIAL OCH KOMPOSITION HAERFOER. AL OCH COMPOSITION HAERFOER
US4225640A (en) * 1978-05-04 1980-09-30 Redmar Investors, Inc. Method of reclaiming thermoplastic materials from municipal waste and product produced thereby
US4225318A (en) * 1978-05-11 1980-09-30 Wrigley Jr Hank J Method of making hydrocarbon composition
US4179270A (en) * 1978-07-27 1979-12-18 Mobil Oil Corporation Aid for kindling fires
US4209561A (en) 1978-07-28 1980-06-24 The United States Of America As Represented By The Administrator Of The National Aeronautics And Space Administration Structural wood panels with improved fire resistance
US4279790A (en) 1979-07-05 1981-07-21 Kabushiki Kaisha Mikuni Seisakusho Composite material compositions using wasterpaper and method of producing same
JPS5856534B2 (en) 1979-08-28 1983-12-15 チッソ株式会社 Polyolefin resin composition
JPS56501053A (en) 1979-08-29 1981-07-30
IN154932B (en) 1979-11-12 1984-12-22 Isaac Dutton Edward
US4302210A (en) * 1979-12-27 1981-11-24 Duncan Norman B Fireplace log
US4328320A (en) * 1980-05-12 1982-05-04 Reszniak Waldemar B Thermoplastic constructional-and-insulating material
US4632795A (en) 1982-11-26 1986-12-30 Wenger Manufacturing, Inc. Method and apparatus for extrusion processing of cellulose bearing materials
US4663103A (en) 1983-08-09 1987-05-05 Collins & Aikman Corporation Apparatus and method of extrusion
DE3485470D1 (en) 1983-10-05 1992-03-05 Nippon Petrochemicals Co Ltd METHOD FOR PRODUCING THERMOPLASTIC PLASTIC FILMS OR PLASTIC FILMS CONTAINING FILLERS.
IT8420722V0 (en) * 1984-02-03 1984-02-03 Francesco Canziani TROLLEY IN PARTICULAR FOR SORTING MACHINES WITH INDEPENDENT OPERATING PLATE.
JPS61151266A (en) 1984-12-25 1986-07-09 Chisso Corp Cellulosic filler for thermoplastic resin
US4772430A (en) * 1985-01-11 1988-09-20 Jgc Corporation Process for compacting and solidifying solid waste materials, apparatus for carrying out the process and overall system for disposal of such waste materials
JPS62169604A (en) * 1985-07-08 1987-07-25 Dai Ichi Kogyo Seiyaku Co Ltd Manufacture of sheet and molded form
US4751034A (en) * 1986-03-14 1988-06-14 Delong Edward A Method of molding using dissociated lignocellulosic material and the product so produced
US4832882A (en) * 1986-11-06 1989-05-23 Synthetics International Corp. Method of removing impurities from a material
US4791020A (en) * 1987-02-02 1988-12-13 Novacor Chemicals Ltd. Bonded composites of cellulose fibers polyethylene
JPS63295800A (en) * 1987-05-22 1988-12-02 株式会社 ヤマトランス Wood powder molded product utilizing pulp and its production
DE3720325A1 (en) * 1987-06-19 1989-01-12 Werner & Pfleiderer DEVICE FOR MIXING AND CONTINUOUSLY EXTRUDING PLASTIC MEASURES
US4885203A (en) * 1987-07-01 1989-12-05 Applied Ultralight Technologies, Inc. Lightweight fired building products
DE3728123A1 (en) * 1987-08-22 1989-03-02 Hoechst Ag METHOD FOR THE PRODUCTION OF FRINGED CELLULOSE MATERIAL, IN PARTICULAR WOOD FIBERS, FOR THE PRODUCTION OF FIBER PANELS
DE3731067A1 (en) * 1987-09-16 1989-04-06 Basf Ag INGREDIENT MOLDING
US4888573A (en) 1988-12-21 1989-12-19 Cooper Industries, Inc. Fuse construction
US5053176A (en) * 1989-11-01 1991-10-01 Variform, Inc. Method and apparatus for creating controlled color patterns in formed vinyl sheet article
US5269991A (en) * 1990-01-17 1993-12-14 L'oreal Process for obtaining mouldings with the appearance of natural stones
US5213021A (en) * 1990-03-14 1993-05-25 Advanced Environmental Recycling Technologies, Inc. Reciprocating cutter assembly
DE4029254A1 (en) * 1990-09-14 1992-03-19 Benecke Ag J H METHOD FOR PRODUCING MULTICOLORED SLUSH SKINS AND FORM AND SEPARATING DEVICE FOR CARRYING OUT THE METHOD
US5413746A (en) * 1992-06-10 1995-05-09 Birjukov; Mikhail V. Method for molding shaped products and an apparatus for carrying out same
US6367197B1 (en) * 1999-08-12 2002-04-09 Quintin W. Saye Irrigation apparatus
US6579605B2 (en) * 2000-07-31 2003-06-17 Crane Plastics Company Llc Multilayer synthetic wood component
US6881367B1 (en) * 2000-11-06 2005-04-19 Elk Composite Building Products, Inc. Composite materials, articles of manufacture produced therefrom, and methods for their manufacture
JP2003026941A (en) * 2001-07-11 2003-01-29 Ajinomoto Co Inc Composition for composite lumber and composite lumber
US6780359B1 (en) * 2002-01-29 2004-08-24 Crane Plastics Company Llc Synthetic wood composite material and method for molding
US6670012B2 (en) * 2002-03-18 2003-12-30 Polyone Corporation Multi-colored coverstock

Patent Citations (99)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2736064A (en) * 1956-02-28 rubin
US1700208A (en) * 1926-11-19 1929-01-29 Paisseau Jean Process and apparatus for production of a substance having a nacreous and chatoyant aspect
US2067012A (en) * 1933-10-09 1937-01-05 Emil C Loetscher Composite building material
US2149066A (en) * 1936-12-09 1939-02-28 Nixon Nitration Works Method for obtaining luster, color, pattern, and complicated shape effects
US2702408A (en) * 1950-07-27 1955-02-22 Union Carbide & Carbon Corp Extrusion of thermoplastic materials
US2744013A (en) * 1952-05-09 1956-05-01 Rodger M Dorland Artificial board
US2832993A (en) * 1952-05-13 1958-05-06 Western Electric Co Apparatus for extruding and cooling plastics
US3023136A (en) * 1956-12-17 1962-02-27 Himmelbeber Max Chipwood articles of high compressive strength and processes for producing the same
US3243327A (en) * 1961-05-16 1966-03-29 Hoppeler Walter Method of making a pressed plate
US3651187A (en) * 1969-10-16 1972-03-21 Hercules Inc Extrusion process
US3875088A (en) * 1971-07-16 1975-04-01 Hasbro Industries Inc Pencil sheath compositions
US4013616A (en) * 1971-11-22 1977-03-22 Wallace Richard A Mixed polymeric structural material and method
US3798294A (en) * 1972-02-10 1974-03-19 Grace W R & Co Method for producing battery separator sheet
US4008858A (en) * 1972-05-12 1977-02-22 Mitsubishi Petrochemical Company Limited Treating device for synthetic resin waste
US4003866A (en) * 1974-01-22 1977-01-18 Etablissements Paturle S.A. Construction material and a process for producing the same
US4011292A (en) * 1974-04-04 1977-03-08 Rowland, Incorporated Method for producing sheet material with multicolor striated pattern and sheet material produced thereby
US4150185A (en) * 1974-11-05 1979-04-17 Joachim Zur Verth Building materials in the form of woodstone panels or sheets and processes for their production
US4250222A (en) * 1974-12-31 1981-02-10 Institut National De Recherche Chimique Appliquee Process for manufacturing finished and semi-finished products from mixtures of various synthetic resin scrap materials
US4018722A (en) * 1975-03-10 1977-04-19 Elizabeth I. Bellack Reclaimed plastic material
US4138534A (en) * 1977-02-07 1979-02-06 Lifetime Foam Products, Inc. Production of structural members from reclaimed polyolefins
US4187352A (en) * 1977-04-19 1980-02-05 Lankhorst Touwfabrieken B.V. Method and apparatus for producing synthetic plastics products, and product produced thereby
US4326854A (en) * 1979-03-09 1982-04-27 Tanner John D Synthetic firelog
US4260573A (en) * 1980-02-07 1981-04-07 Kenneth Overman Method for pelletizing wood particulate matter
US4323625A (en) * 1980-06-13 1982-04-06 Monsanto Company Composites of grafted olefin polymers and cellulose fibers
US4510278A (en) * 1981-04-07 1985-04-09 Methanol Chemie Nederland V.O.F. Manufacture of chipboard and a novel suitable bonding agent
US4376144A (en) * 1981-04-08 1983-03-08 Monsanto Company Treated fibers and bonded composites of cellulose fibers in vinyl chloride polymer characterized by an isocyanate bonding agent
US4379525A (en) * 1981-08-06 1983-04-12 Owens-Illinois, Inc. Process for recycling plastic container scrap
US4797242A (en) * 1983-03-29 1989-01-10 Mitsui Toatsu Chemicals, Incorporated Method for shaping thermosetting resins
US4656722A (en) * 1983-07-25 1987-04-14 Larry Armstrong Method of forming a decorative panel of molded plastic
US4717742A (en) * 1985-05-29 1988-01-05 Beshay Alphons D Reinforced polymer composites with wood fibers grafted with silanes - grafting of celluloses or lignocelluloses with silanes to reinforce the polymer composites
US4738808A (en) * 1985-11-18 1988-04-19 Hammer Floyd V Method of forming articles from a plastic material
US4824627A (en) * 1985-11-18 1989-04-25 Floyd V. Hammer Method of making a molded plastic product
US4822826A (en) * 1986-09-04 1989-04-18 La Cellulose Du Pin Composite material and method of manufacturing same
US4812368A (en) * 1987-01-07 1989-03-14 Basf Aktiengesellschaft Process for the preparation of lightweight, planar molded articles
US4999390A (en) * 1987-02-16 1991-03-12 Novopan Traeindustri A/S Composite board and a method and a composition for its production
US4915764A (en) * 1987-05-23 1990-04-10 Mario Miani Method of making panels
US4913863A (en) * 1989-01-30 1990-04-03 Hoechst Celanese Corporation Split extrusion die assembly for thermoplastic materials and methods of using the same
US5387381A (en) * 1989-12-07 1995-02-07 Alcan Aluminum Corporation Method for extruding plastic with accent color pattern
US5082605A (en) * 1990-03-14 1992-01-21 Advanced Environmental Recycling Technologies, Inc. Method for making composite material
US5088910A (en) * 1990-03-14 1992-02-18 Advanced Environmental Recycling Technologies, Inc. System for making synthetic wood products from recycled materials
US5096046A (en) * 1990-03-14 1992-03-17 Advanced Environmental Recycling Technologies, Inc. System and process for making synthetic wood products from recycled materials
US5096406A (en) * 1990-03-14 1992-03-17 Advanced Environmental Recycling Technologies, Inc. Extruder assembly for composite materials
US5084135A (en) * 1990-03-27 1992-01-28 Advanced Environmental Recycling Technologies, Inc. Recycling plastic coated paper product waste
US5277758A (en) * 1990-03-27 1994-01-11 Advanced Environmental Recycling Technologies, Inc. Method for recycling plastic coated paper product waste and polymeric film
US5502088A (en) * 1991-12-18 1996-03-26 Hododi; Andrei Wood substitute based on lignocellulosic and inorganic materials, method for obtaining the same and use
US6210792B1 (en) * 1992-08-31 2001-04-03 Andersen Corporation Advanced compatible polymer wood fiber composite
US6015611A (en) * 1992-08-31 2000-01-18 Andersen Corporation Advanced polymer wood composite
US5486553A (en) * 1992-08-31 1996-01-23 Andersen Corporation Advanced polymer/wood composite structural member
US6015612A (en) * 1992-08-31 2000-01-18 Andersen Corporation Polymer wood composite
US5497594A (en) * 1992-09-01 1996-03-12 Andersen Corporation Advanced polymer and wood fiber composite structural component
US5406768A (en) * 1992-09-01 1995-04-18 Andersen Corporation Advanced polymer and wood fiber composite structural component
US5620642A (en) * 1993-03-05 1997-04-15 Misawa Homes Co., Ltd. Simulated wood product manufacturing method and simulated wood product
US5725939A (en) * 1994-02-10 1998-03-10 Ein Engineering Co., Ltd. Synthetic wood meal, method and apparatus for manufacturing the same; synthetic wood board including the synthetic wood meal, method and apparatus of extrusion molding therefor
US5480602A (en) * 1994-06-17 1996-01-02 Nagaich; Laxmi Extruded particle board
US6344509B1 (en) * 1994-12-22 2002-02-05 Taiyo Kagaku Co., Ltd. Thermoplastic resin compositions
US5603883A (en) * 1995-04-19 1997-02-18 Lenzing Aktiengesellschaft Process of and apparatus for making celluose products
US5624620A (en) * 1995-05-03 1997-04-29 Turner; James E. Process for making non-extruded molded boards and sheet products
US6011091A (en) * 1996-02-01 2000-01-04 Crane Plastics Company Limited Partnership Vinyl based cellulose reinforced composite
US5869176A (en) * 1996-04-03 1999-02-09 M. A. Hannacolor, A Division Of M. A. Hanna Company Composition and method for extruding plastic articles having accent color pattern and comprising poly-α-methylstyrene pellets
US5882564A (en) * 1996-06-24 1999-03-16 Andersen Corporation Resin and wood fiber composite profile extrusion method
US6984676B1 (en) * 1996-10-22 2006-01-10 Crane Plastics Company Llc Extrusion of synthetic wood material
US5866264A (en) * 1996-10-22 1999-02-02 Crane Plastics Company Limited Partnership Renewable surface for extruded synthetic wood material
US6180257B1 (en) * 1996-10-29 2001-01-30 Crane Plastics Company Limited Partnership Compression molding of synthetic wood material
US6511757B1 (en) * 1996-10-29 2003-01-28 Crane Plastics Company Llc Compression molding of synthetic wood material
US6344504B1 (en) * 1996-10-31 2002-02-05 Crane Plastics Company Limited Partnership Extrusion of synthetic wood material
US6035588A (en) * 1996-11-21 2000-03-14 Crane Plastics Company Limited Partnership Deck plank
US6357197B1 (en) * 1997-02-05 2002-03-19 Andersen Corporation Polymer covered advanced polymer/wood composite structural member
US6531010B2 (en) * 1997-03-28 2003-03-11 Andersen Corporation Thermoplastic resin and fiberglass fabric composite and method
US6682814B2 (en) * 1997-05-30 2004-01-27 Andersen Corporation Fiber-polymeric composite siding unit and method of manufacture
US20030032702A1 (en) * 1997-09-02 2003-02-13 Marshall Medoff Compositions and composites of cellulosic and lignocellulosic materials and resins, and methods of making the same
US6685858B2 (en) * 1997-09-05 2004-02-03 Crane Plastics Company Llc In-line compounding and extrusion system
US20030025233A1 (en) * 1997-09-05 2003-02-06 Crane Plastics Company Llc In-line compounding and extrusion system
US6379815B1 (en) * 1997-10-20 2002-04-30 Syntech Holdings B.V. Moulded element, in particular in the shape of a plate, which is a compressed mixture of binder and filler, a method and a device for manufacturing such a moulded elements, as well as floor plates, a sports hall provided with such floor
US6207729B1 (en) * 1997-10-31 2001-03-27 Xyleco, Inc. Texturized cellulosic and lignocellulosic materials and compositions and composites made therefrom
US6726464B1 (en) * 1997-12-04 2004-04-27 Misawa Homes Co. Mixing device for manufacturing molding
US6054207A (en) * 1998-01-21 2000-04-25 Andersen Corporation Foamed thermoplastic polymer and wood fiber profile and member
US6342172B1 (en) * 1998-01-21 2002-01-29 Andersen Corporation Method of forming a foamed thermoplastic polymer and wood fiber profile and member
US6344268B1 (en) * 1998-04-03 2002-02-05 Certainteed Corporation Foamed polymer-fiber composite
US20020005602A1 (en) * 1998-07-20 2002-01-17 Jacobsen William W. Lignocellulose fiber filler for thermoplastic composite compositions
US6695874B2 (en) * 1998-08-24 2004-02-24 Radiant Medical, Inc. Method and system for control of a patient's body temperature by way of transluminally insertable heat exchange catheter
US20020033563A1 (en) * 1998-11-12 2002-03-21 Certainteed Corporation. Apparatus for continuous forming shaped polymeric articles
US6337138B1 (en) * 1998-12-28 2002-01-08 Crane Plastics Company Limited Partnership Cellulosic, inorganic-filled plastic composite
US6376582B1 (en) * 1999-03-29 2002-04-23 Yamaha Corporation Wood fiberboard and manufacturing method therefor
US6680090B2 (en) * 1999-04-16 2004-01-20 Andersen Corporation Polyolefin wood fiber composite
US6682789B2 (en) * 1999-04-16 2004-01-27 Andersen Corporation Polyolefin wood fiber composite
US20030036589A1 (en) * 2000-04-26 2003-02-20 Archuletta Phil T. Method for making wood and plastic composite material
US20030071389A1 (en) * 2000-05-14 2003-04-17 Manning Mark J. Lignocellulosic composites
US6722082B1 (en) * 2000-06-28 2004-04-20 Andersen Corporation Window having a hinged weatherstrip
US20020049266A1 (en) * 2000-08-22 2002-04-25 Ajinomoto Co., Inc. Woody thermoplastic resin composition
US6718704B2 (en) * 2000-11-01 2004-04-13 Andersen Corporation Attachment system for a decorative member
US6708504B2 (en) * 2001-01-19 2004-03-23 Crane Plastics Company Llc Cooling of extruded and compression molded materials
US6526712B2 (en) * 2001-05-21 2003-03-04 Advanced Environmental Recycling Technologies, Inc. Extruded composite interlocking corner assembly
US20030021915A1 (en) * 2001-06-15 2003-01-30 Vivek Rohatgi Cellulose - polymer composites and related manufacturing methods
US20030004232A1 (en) * 2001-06-28 2003-01-02 Certainteed Corporation Non-staining polymer composite product
USD488243S1 (en) * 2001-07-06 2004-04-06 Andersen Corporation Door sill portion
US20030030176A1 (en) * 2001-07-13 2003-02-13 Monovoukas Yiannis A. Cellulose-reinforced thermoplastic composite and methods of making same
US6865849B1 (en) * 2002-01-24 2005-03-15 Crane Plastics Company Llc Top course molding
US20040038002A1 (en) * 2002-08-21 2004-02-26 Sandro Franco Extruded wood imitation component and process
US20050053767A1 (en) * 2002-08-21 2005-03-10 Sandro Franco Extruded wood imitation component and process

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20080093763A1 (en) * 2006-10-06 2008-04-24 Douglas Mancosh Multi-color fiber-plastic composites and systems and methods for their fabrication

Also Published As

Publication number Publication date
MXPA06014301A (en) 2007-05-04
US20050271872A1 (en) 2005-12-08
US20060068215A2 (en) 2006-03-30
US7410687B2 (en) 2008-08-12
US20050271889A1 (en) 2005-12-08
US20070087180A1 (en) 2007-04-19

Similar Documents

Publication Publication Date Title
US7410687B2 (en) Variegated composites and related methods of manufacture
CA2708664C (en) Method of making cellulosic - thermoplastic composites of an anhydride containing copolymer
US7473722B2 (en) Polymer-fiber composite building material with bulk and aesthetically functional fillers
US20070154689A1 (en) Composite products contaning a transparent or translucent capstock
US8088840B2 (en) Polymer-fiber composite building material with bulk and aesthetically functional fillers
US11370894B2 (en) Composite product and a process for producing said product
US20080299351A1 (en) Non-wood building materials with simulated wood-grain surface appearance
AU2004249706A1 (en) Biopolymer structures and components
US9394432B1 (en) Composite members and methods for producing same
KR101859142B1 (en) Anti fungal synthetic wood composition and preparing method thereof
CN103351632A (en) Anti-termite-type wood plastic composite material and preparation process therefor
CA2568873A1 (en) Improved variegated composites and related methods of manufacture
CA2653722A1 (en) Microbial resistant composites
EP1816160B1 (en) Method of fabricating light-stabilized coloured wood-polymer composite materials suitable for structural members
US9382398B1 (en) Composite members and methods for producing same
CA2914994A1 (en) Wood-plastic composite material
KR20120009093A (en) A tining method for prevention discolor of synthetic wood
ZA200510128B (en) Biopolymer structures and components
US20200385553A1 (en) Composite building materials
KR101854866B1 (en) synthetic wood composition with discoloration-resistance and preparing method thereof
US20060061004A1 (en) Extrusion process and decorative synthetic lumber produced therefrom
WO2006019517A2 (en) Thermal stabilization of biocides in matrix compositions processed at elevated temperatures
Pilarski Durability of wood-plastic composites exposed to freeze-thaw cycling
TWM587172U (en) Composite plastic alloy structure
BG1454U1 (en) Composition for cellulose-polymer composite

Legal Events

Date Code Title Description
STCB Information on status: application discontinuation

Free format text: ABANDONED -- FAILURE TO RESPOND TO AN OFFICE ACTION

AS Assignment

Owner name: BRANCH BANKING AND TRUST COMPANY, AS COLLATERAL AG

Free format text: SECURITY AGREEMENT;ASSIGNOR:TREX COMPANY, INC.;REEL/FRAME:023620/0786

Effective date: 20091104