WO2012121970A2 - Cycle time reduction masterbatches and their use in thermoplastic compounds - Google Patents

Cycle time reduction masterbatches and their use in thermoplastic compounds Download PDF

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Publication number
WO2012121970A2
WO2012121970A2 PCT/US2012/027277 US2012027277W WO2012121970A2 WO 2012121970 A2 WO2012121970 A2 WO 2012121970A2 US 2012027277 W US2012027277 W US 2012027277W WO 2012121970 A2 WO2012121970 A2 WO 2012121970A2
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WO
WIPO (PCT)
Prior art keywords
masterbatch
plastic article
cinders
fly ash
thermoplastic resin
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.)
Ceased
Application number
PCT/US2012/027277
Other languages
French (fr)
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WO2012121970A3 (en
Inventor
Jason D. PIUNTI
Jack R. Prince
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.)
Revolutionary Plastics LLC
Avient Corp
Original Assignee
Polyone Corp
Revolutionary Plastics LLC
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 Polyone Corp, Revolutionary Plastics LLC filed Critical Polyone Corp
Priority to US14/002,629 priority Critical patent/US9290645B2/en
Publication of WO2012121970A2 publication Critical patent/WO2012121970A2/en
Publication of WO2012121970A3 publication Critical patent/WO2012121970A3/en
Anticipated expiration legal-status Critical
Ceased legal-status Critical Current

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Classifications

    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L23/00Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers
    • C08L23/02Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers not modified by chemical after-treatment
    • C08L23/04Homopolymers or copolymers of ethene
    • C08L23/06Polyethene
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B29WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29CSHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
    • B29C43/00Compression moulding, i.e. applying external pressure to flow the moulding material; Apparatus therefor
    • B29C43/22Compression moulding, i.e. applying external pressure to flow the moulding material; Apparatus therefor of articles of indefinite length
    • B29C43/24Calendering
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B29WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29CSHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
    • B29C45/00Injection moulding, i.e. forcing the required volume of moulding material through a nozzle into a closed mould; Apparatus therefor
    • B29C45/0013Injection moulding, i.e. forcing the required volume of moulding material through a nozzle into a closed mould; Apparatus therefor using fillers dispersed in the moulding material, e.g. metal particles
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B29WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29CSHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
    • B29C48/00Extrusion moulding, i.e. expressing the moulding material through a die or nozzle which imparts the desired form; Apparatus therefor
    • B29C48/001Combinations of extrusion moulding with other shaping operations
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B29WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29CSHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
    • B29C48/00Extrusion moulding, i.e. expressing the moulding material through a die or nozzle which imparts the desired form; Apparatus therefor
    • B29C48/022Extrusion moulding, i.e. expressing the moulding material through a die or nozzle which imparts the desired form; Apparatus therefor characterised by the choice of material
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08JWORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
    • C08J3/00Processes of treating or compounding macromolecular substances
    • C08J3/20Compounding polymers with additives, e.g. colouring
    • C08J3/22Compounding polymers with additives, e.g. colouring using masterbatch techniques
    • C08J3/226Compounding polymers with additives, e.g. colouring using masterbatch techniques using a polymer as a carrier
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B29WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29CSHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
    • B29C48/00Extrusion moulding, i.e. expressing the moulding material through a die or nozzle which imparts the desired form; Apparatus therefor
    • B29C48/03Extrusion moulding, i.e. expressing the moulding material through a die or nozzle which imparts the desired form; Apparatus therefor characterised by the shape of the extruded material at extrusion
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B29WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29CSHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
    • B29C48/00Extrusion moulding, i.e. expressing the moulding material through a die or nozzle which imparts the desired form; Apparatus therefor
    • B29C48/03Extrusion moulding, i.e. expressing the moulding material through a die or nozzle which imparts the desired form; Apparatus therefor characterised by the shape of the extruded material at extrusion
    • B29C48/07Flat, e.g. panels
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B29WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29CSHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
    • B29C48/00Extrusion moulding, i.e. expressing the moulding material through a die or nozzle which imparts the desired form; Apparatus therefor
    • B29C48/03Extrusion moulding, i.e. expressing the moulding material through a die or nozzle which imparts the desired form; Apparatus therefor characterised by the shape of the extruded material at extrusion
    • B29C48/07Flat, e.g. panels
    • B29C48/08Flat, e.g. panels flexible, e.g. films
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B29WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29CSHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
    • B29C48/00Extrusion moulding, i.e. expressing the moulding material through a die or nozzle which imparts the desired form; Apparatus therefor
    • B29C48/03Extrusion moulding, i.e. expressing the moulding material through a die or nozzle which imparts the desired form; Apparatus therefor characterised by the shape of the extruded material at extrusion
    • B29C48/09Articles with cross-sections having partially or fully enclosed cavities, e.g. pipes or channels

Definitions

  • This invention relates to use of a master batch to deliver a functional filler of fly ash and/or cinders into plastic articles made of thermoplastic compounds.
  • Fly ash and cinders are by-products of combustion. Fly ash and cinders can be separated into specific particle sizes. Revolutionary Plastics, LLC is a supplier of fly ash and cinders having specific particles sizes and the owner of U.S. Pat. No. 7,879,939 (Prince et al.), which is incorporated by reference as if fully rewritten herein.
  • thermoplastic compounds such as identified in Table 1, in which the fly ash and/or cinders component constitutes 1-40 weight percent of the compound for a foamed article and in which the fly ash and/or cinders component can constitute 1-70 weight percent of the compound for an un-foamed article.
  • fly ash and/or cinders can be an excellent functional filler for all the reasons described therein. But fly ash and cinders can also be abrasive, and without special handling equipment and care during manufacture, conventional compounding equipment handling fly ash and cinders particulates can become worn more quickly.
  • fly ash and/or cinders filler in a pelletized form at the time of molding, extruding, or calendering to shape the final plastic article.
  • Fly ash and/or cinders particulate is not suitable for molding equipment, especially injection molding equipment.
  • the present invention solves these problems by providing a masterbatch comprising functional filler of any of (a) fly ash, (b) cinders, or (c) fly ash and cinders, which functional filler can be used to reduce molding cycle time or extruding or calendering throughput without loss of physical properties of the polymer compound. Also the fly ash and/or cinders, products of combustion, are consumed in a sustainable manner.
  • One aspect of the invention is a masterbatch for a thermoplastic compound having a first thermoplastic resin, comprising (a) fly ash and/or cinders and (b) a second thermoplastic resin, compatible with or the same as the first thermoplastic resin, to serve as a carrier for the fly ash and/or cinders, wherein the fly ash and/or cinders comprises at least 50 percent by weight of the masterbatch.
  • Another aspect of the invention is a method of using the masterbatch identified in the paragraph above.
  • thermoplastic resin is a candidate for use with fly ash and/or cinders according of the invention.
  • large volume commercial thermoplastic resins include polyolefins, polyamides, polyesters, poly (meth)acrylates, polycarbonates, poly(vinyl halides), polyvinyl alcohols, polynitriles, polyacetals, polyimides, polyarylketones, polyetherketones, polyhydroxyalkanoates, polycaprolactones, polystyrenes, polyurethanes, polysulfones, polyphenylene oxides, polyphenylene sulfides, polyacetates, liquid crystal polymers, fluoropolymers, ionomeric polymers, and copolymers of any of them and combinations of any two or more of them.
  • thermoplastic resins include acrylonitrile butadiene styrene (ABS), polymethyl methacrylate (PMMA), cellulose acetate, cyclic olefin copolymer (COC), ethylene-vinyl acetate (EVA), ethylene vinyl alcohol (EVOH), polytetrafluoroethane (PTFE), ionomers, polyoxymethylene (POM or Acetal), polyacrylonitrile (PAN), polyamide 6, polyamide 6,6, polyamide-imide (PAI), polyaryletherketone (PAEK), polybutadiene (PBD), polybutylene (PB), polybutylene terephthalate (PBT), polycaprolactone (PCL),
  • PCTFE polychlorotrifluoroethylene
  • PET polyethylene terephthalate
  • PCT polycyclohexylene dimethylene terephthalate
  • PCT polycarbonate
  • PHB polyhydroxybutyrate
  • PE polyethylene
  • PEEK polyetheretherketone
  • PEKK polyetherketoneketone
  • PEI polyethersulfone
  • CPE chlorinated polyethylene
  • PI polyimide
  • PLA polylactic acid
  • PMP polymethylpentene
  • PPO polyphenylene oxide
  • PPS polyphenylene sulfide
  • PPS polyphthalamide
  • PPA polypropylene
  • PP polysulfone
  • PSU polytrimethylene terephthalate
  • PPU polyurethane
  • PU polyvinyl acetate
  • PVDC polyvinylidene chloride
  • SAN styrene-acrylonitrile
  • thermoplastic resin can be prime or reprocessed via recycling.
  • the use of recycled thermoplastic resin further can reduce costs for the manufacturer and provides additional sustainable solutions for the environment.
  • fly ash and/or cinders means that the functional filler can be selected from the group consisting of fly ash, cinders, and both fly ash and cinders.
  • Fly ash and/or cinders are by-products of coal combustion and have been found in this invention to be an unexpectedly valuable filler to perform the function of reducing of molding cycle times without loss of physical properties.
  • Fly ash useful in this invention is registered as CAS No. 71243-67-9.
  • fly ash constitutes a multiplicity of spheres of a mineral composite formed during coal combustion.
  • cinders are other residue particulates formed during coal combustion, such as fused or vitrified matter.
  • Preferred grades of fly ash and/or cinders have been processed to result in the following properties: a melting point or greater than about 1090°C; a specific gravity of from about 2.2 to about 2.8; less than 100 parts per million of lead, hexavalent chromium, mercury or cadmium, a moisture content of 1% or less; a polycyclic aromatic hydrocarbon content of less than about 200 parts per million; a crystalline silica content of below about 0.5%; and a particle size range in which about 85% of the particles fall within 0.2 ⁇ - 280 ⁇ , and remainder are less than about 850 ⁇ .
  • the masterbatch of the present invention can include
  • plastics additives in an amount that is sufficient to obtain a desired processing or performance property for the masterbatch or the final molded, extruded, or calendered compound.
  • the amount of additive(s) should not be wasteful of the additive nor detrimental to the processing or performance of the compound.
  • Those skilled in the art of thermoplastics compounding without undue experimentation but with reference to such treatises as Plastics Additives Database (2004) from Plastics Design Library (www.williamandrew.com), can select from many different types of additives for inclusion into the compounds of the present invention.
  • Non-limiting examples of optional additives include adhesion promoters; biocides (antibacterials, fungicides, and mildewcides), anti-fogging agents; anti-static agents; bonding, blowing and foaming agents; dispersants; fillers and extenders; fire and flame retardants and smoke suppresants; impact modifiers; initiators; lubricants; micas; pigments, colorants and dyes;
  • plasticizers processing aids; release agents; silanes, titanates and zirconates; slip and anti-blocking agents; stabilizers; stearates; ultraviolet light absorbers; viscosity regulators; waxes; and combinations of them.
  • the fly ash and/or cinders to be prepared into the form of a masterbatch with weight percent of the fly ash and/or cinders being at least 50 percent, desirably from about 72 to about 90 percent, and preferably from about 75 to about 85 percent by weight of the masterbatch.
  • the weight percent of fly ash and/or cinders desirably can be any percentage between 72 and 90 percent, stated in any range of two percents within that range.
  • the carrier for the fly ash and/or cinders in the form of a masterbatch can be any plastic resin which is compatible with the plastic resin into which the masterbatch will be added, including any of the thermoplastic polymers identified above.
  • LLDPE linear low density polyethylene
  • MDPE medium density polyethylene
  • any of the additives identified above can be added to the masterbatch for later melt mixing with the plastic resin and other ingredients to be used to make the final plastic compound, whether molded, extruded, or calendered.
  • mixing in a continuous process typically occurs in an extruder that is elevated to a temperature that is sufficient to melt the polymer matrix with addition either at the head of the extruder or downstream in the extruder of the solid ingredient additives.
  • Extruder speeds can range from about 50 to about 500 revolutions per minute (rpm), and preferably from about 100 to about 300 rpm.
  • the output from the extruder is pelletized for later extrusion, molding, or calendering into polymeric articles.
  • mixing in a batch process typically occurs in a Banbury or other batch mixer that is also elevated to a temperature that is sufficient to melt the polymer matrix to permit addition of the solid ingredient additives.
  • the mixing speeds range from 60 to 1000 rpm.
  • the output from the mixer is chopped into smaller sizes for later extrusion, molding, or calendering into polymeric articles.
  • Masterbatches of carrier resin and fly ash and/or cinders can be purchased from PolyOne Corporation, as a distributor of Revolutionary Plastics, under the brand of Nano P.E.A.TM nano-sized polymer enhancing agent.
  • the melt flow rate can range from about 5 to about 9 and preferably from about 5 to about 7 g/10 min.
  • Moisture can range from about 100 to about 1000 ppm.
  • the specific gravity can range from about 1.6 to about 1.8 and preferably from about 1.74 to about 1.78.
  • the masterbatches are typically cut into pellets in a diameter of from about 2.5 mm to about 3.8 mm.
  • a presently preferred grade of Nano P.E.A. is LLH7506 concentrate, which uses about 25 weight percent MDPE as a carrier and has about 75 weight percent of fly ash and cinders.
  • the reshaping step includes pressurized injecting, holding, and cooling steps before the plastic article is ejected, the cycle of which the time is being measured to determine cycle time. More specifically, the reshaping step comprises four substeps of (1) injecting the compound into a mold; (2) holding the compound in the mold to form the plastic article in the shape of the mold; (3) cooling the plastic article to permit the plastic article to be released from the mold while retaining shape of the mold; and (4) ejecting the plastic article.
  • the time between commencement of the injecting substep (1) and commencement of the ejecting substep (4) is one cycle time, and the cycle time of the compound is reduced from about 5 percent to about 30 percent for a plastic article of the compound as compared with a cycle time between commencement of substep (1) and commencement substep (4) for a plastic article that only contains the plastic resin without the masterbatch present.
  • the amount of masterbatch in the final polymer compound can range from about 1 to about 65 and preferably from about 20 to about 40 weight percent.
  • the weight percent of the fly ash and/or cinders functional filler in the final polymer compound can range from about 1 to about 58, desirably from about 5 to about 44, and preferably from about 10 to about 32 weight percent.
  • Masterbatches of the present invention mixed with thermoplastic resin can be molded, extruded, or calendered with surprising efficiency and result in plastic articles having excellent physical properties and appearance.
  • molding cycle times can be reduced by from about 5 percent to about 30 percent and preferably at least about 14 percent merely because of the presence of the fly ash and/or cinders as functional fillers, all other factors being equal.
  • the fly ash and/or cinders functional filler can replace as much as about 65% of the plastic resin without unacceptable loss of physical properties. With the cost of the fly ash and/or cinders possibly being less than the cost of the plastic resin being replaced, less expensive molded, extruded, or calendered plastic articles can be made, without unacceptable loss of physical properties or sacrifice of ultimate surface appearance.
  • any number of plastic articles can be benefit from the use of fly ash and/or cinders in the preparation of the polymer compound.
  • final plastic articles which can benefit from the invention include appliances (refrigerators, freezers, washers, dryers, toasters, blenders, vacuum cleaners, coffee makers, mixers); building and construction articles (fences, decks and rails, floors, floor covering, pipes and fittings, siding, trim, windows, window shutters, doors, molding, plumbing products, toilet seats, and wall coverings); consumer goods (power hand tools, rakes, shovels, lawn mowers, shoes, boots, golf clubs, fishing poles, and watercraft); electrical/electronic (printers, computer housings, business equipment, LCD projectors, mobile phones, connectors, chip trays, circuit breakers, and plugs); healthcare products (wheelchairs, beds, testing equipment, and packaging); industrial products (containers, bottles, drums, material handling, gears, bearings, gaskets and seals, valves, wind
  • a preferred means of using masterbatches of the invention is to have them introduced into the core sections of an extruded or molded article.
  • Prince et al. identified above describes how a fly-ash- and/or cinders-containing compound can be used in an extruded core section, which is full enclosed by a protective cladding, by manufacture using a co-extruder, to make a window shutter frame, louvers, or stiles or other elongated articles.
  • Example 1 below proves successful injection molding of a core section.
  • a commercially available plastic article was molded in a two component mold having a core section of regrind/recycled polyolefins ( a mixture of polypropylene and polyethylene resins) and other ingredients comprising 40 weight percent of the article and a capstock section of prime polypropylene, enveloping the core section, comprising 60 weight percent of the article.
  • the injection molding machine was operated in accordance with standard operating conditions for the molding of that particular style and shape of that plastic article.
  • the applicable cycle time measured from commencement of the injecting step to commencement of the ejecting step was 116.5 seconds.
  • Example 1 The same plastic article was molded in the same injection molding machine operated in accordance with the same operating conditions with the same capstock section but with a core section comprising 37 weight percent of a masterbatch of LLH 7506 Nano P.E.A.TM polymer enhancing agent from Revolutionary Plastics LLC and the remaining 63 weight percent of the same regrind/recycled polyolefins and the other ingredients as contained in the core section of Comparative Example A. Overall, the masterbatch comprised 14.8% of the entire plastic article. The applicable cycle time measured was 99.5 seconds, a startling 14.59 percent improvement over the cycle time of
  • Example 1 plastic article The properties and appearance of the Example 1 plastic article were determined by the molder to be acceptable for commercial production and sale. In other words, to a skilled observer, no change in appearance or end-use properties was noticeable.
  • Example 1 over Comparative Example A, over only 24 hours, 127 more plastic articles could be made, all other factors being equal. That greater productivity extrapolates into 889 more plastic articles per week, 3,810 per 30-day month, and 46,355 more per year.

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Abstract

A masterbatch for a thermoplastic compound is disclosed, comprising fly ash and/or cinders and a carrier thermoplastic resin, compatible with or the same as the thermoplastic resin used in the compound. The amount of fly ash and/or cinders comprises at least 50 percent by weight of the masterbatch. Presence of the fly ash and/or cinders can reduce cycle time for molding of the compound into a plastic article by from about 5 percent to about 30 percent merely because of the presence of the fly ash and/or cinders.

Description

CYCLE TIME REDUCTION MASTERBATCHES AND THEIR USE IN THERMOPLASTIC COMPOUNDS
CLAIM OF PRIORITY
[0001] This application claims priority from U.S. Provisional Patent
Application Serial Number 61/449,613 bearing Attorney Docket Number 12011005 and filed on March 4, 2011, which is incorporated by reference.
FIELD OF THE INVENTION
[0002] This invention relates to use of a master batch to deliver a functional filler of fly ash and/or cinders into plastic articles made of thermoplastic compounds.
BACKGROUND OF THE INVENTION
[0003] Fly ash and cinders are by-products of combustion. Fly ash and cinders can be separated into specific particle sizes. Revolutionary Plastics, LLC is a supplier of fly ash and cinders having specific particles sizes and the owner of U.S. Pat. No. 7,879,939 (Prince et al.), which is incorporated by reference as if fully rewritten herein.
[0004] Prince et al. discloses preparation of fully formulated
thermoplastic compounds, such as identified in Table 1, in which the fly ash and/or cinders component constitutes 1-40 weight percent of the compound for a foamed article and in which the fly ash and/or cinders component can constitute 1-70 weight percent of the compound for an un-foamed article.
SUMMARY OF THE INVENTION
[0005] What is needed is a functional filler for polymer compounds that reduces cycle time of molding operations and reduces unit production costs but maintains physical properties of the unfilled plastic compound. [0006] As explained by Prince et al., fly ash and/or cinders can be an excellent functional filler for all the reasons described therein. But fly ash and cinders can also be abrasive, and without special handling equipment and care during manufacture, conventional compounding equipment handling fly ash and cinders particulates can become worn more quickly.
[0007] Therefore, what is especially needed is a masterbatch to introduce the functional fly ash and/or cinders filler in a pelletized form at the time of molding, extruding, or calendering to shape the final plastic article. Fly ash and/or cinders particulate is not suitable for molding equipment, especially injection molding equipment.
[0008] The present invention solves these problems by providing a masterbatch comprising functional filler of any of (a) fly ash, (b) cinders, or (c) fly ash and cinders, which functional filler can be used to reduce molding cycle time or extruding or calendering throughput without loss of physical properties of the polymer compound. Also the fly ash and/or cinders, products of combustion, are consumed in a sustainable manner.
[0009] One aspect of the invention is a masterbatch for a thermoplastic compound having a first thermoplastic resin, comprising (a) fly ash and/or cinders and (b) a second thermoplastic resin, compatible with or the same as the first thermoplastic resin, to serve as a carrier for the fly ash and/or cinders, wherein the fly ash and/or cinders comprises at least 50 percent by weight of the masterbatch.
[00010] Another aspect of the invention is a method of using the masterbatch identified in the paragraph above.
[00011] The following embodiments explain some attributes of the invention.
EMBODIMENTS OF THE INVENTION
[00012] Thermoplastic Resins for Polymer Compounds [00013] Any thermoplastic resin is a candidate for use with fly ash and/or cinders according of the invention. Non-limiting examples of large volume commercial thermoplastic resins include polyolefins, polyamides, polyesters, poly (meth)acrylates, polycarbonates, poly(vinyl halides), polyvinyl alcohols, polynitriles, polyacetals, polyimides, polyarylketones, polyetherketones, polyhydroxyalkanoates, polycaprolactones, polystyrenes, polyurethanes, polysulfones, polyphenylene oxides, polyphenylene sulfides, polyacetates, liquid crystal polymers, fluoropolymers, ionomeric polymers, and copolymers of any of them and combinations of any two or more of them.
[00014] Published literature exists to identify many commercial species of these categories of thermoplastic resins. Non-limiting examples of specific commercial thermoplastic resins include acrylonitrile butadiene styrene (ABS), polymethyl methacrylate (PMMA), cellulose acetate, cyclic olefin copolymer (COC), ethylene-vinyl acetate (EVA), ethylene vinyl alcohol (EVOH), polytetrafluoroethane (PTFE), ionomers, polyoxymethylene (POM or Acetal), polyacrylonitrile (PAN), polyamide 6, polyamide 6,6, polyamide-imide (PAI), polyaryletherketone (PAEK), polybutadiene (PBD), polybutylene (PB), polybutylene terephthalate (PBT), polycaprolactone (PCL),
polychlorotrifluoroethylene (PCTFE), polyethylene terephthalate (PET), polycyclohexylene dimethylene terephthalate (PCT), polycarbonate (PC), polyhydroxybutyrate (PHB), polyethylene (PE), polyetheretherketone (PEEK), polyetherketoneketone (PEKK), polyetherimide (PEI), polyethersulfone (PES), chlorinated polyethylene (CPE), polyimide (PI), polylactic acid (PLA), polymethylpentene (PMP), polyphenylene oxide (PPO), polyphenylene sulfide (PPS), polyphthalamide (PPA), polypropylene (PP), polysulfone (PSU), polytrimethylene terephthalate (PTT), polyurethane (PU), polyvinyl acetate (PVA), polyvinyl chloride (PVC), polyvinylidene chloride (PVDC), and styrene-acrylonitrile (SAN). [00015] These specific thermoplastic resins can be substituted or unsubstituted and mixed in any combination suitable to any person having ordinary skill in the art.
[00016] The quality of the thermoplastic resin can be prime or reprocessed via recycling. The use of recycled thermoplastic resin further can reduce costs for the manufacturer and provides additional sustainable solutions for the environment.
[00017] Functional Filler
[00018] As used herein, "fly ash and/or cinders" means that the functional filler can be selected from the group consisting of fly ash, cinders, and both fly ash and cinders.
[00019] Fly ash and/or cinders are by-products of coal combustion and have been found in this invention to be an unexpectedly valuable filler to perform the function of reducing of molding cycle times without loss of physical properties. Fly ash useful in this invention is registered as CAS No. 71243-67-9.
[00020] Stated most generally, fly ash constitutes a multiplicity of spheres of a mineral composite formed during coal combustion. Stated most generally, cinders are other residue particulates formed during coal combustion, such as fused or vitrified matter. Preferred grades of fly ash and/or cinders have been processed to result in the following properties: a melting point or greater than about 1090°C; a specific gravity of from about 2.2 to about 2.8; less than 100 parts per million of lead, hexavalent chromium, mercury or cadmium, a moisture content of 1% or less; a polycyclic aromatic hydrocarbon content of less than about 200 parts per million; a crystalline silica content of below about 0.5%; and a particle size range in which about 85% of the particles fall within 0.2 μιη - 280 μιη, and remainder are less than about 850 μιη.
[00021] Fly ash and/or cinders of a variety of grades and treatments can be purchased from Revolutionary Plastics LLC of Las Vegas, Nevada. [00022] Optional Additives
[00023] The masterbatch of the present invention can include
conventional plastics additives in an amount that is sufficient to obtain a desired processing or performance property for the masterbatch or the final molded, extruded, or calendered compound. The amount of additive(s) should not be wasteful of the additive nor detrimental to the processing or performance of the compound. Those skilled in the art of thermoplastics compounding, without undue experimentation but with reference to such treatises as Plastics Additives Database (2004) from Plastics Design Library (www.williamandrew.com), can select from many different types of additives for inclusion into the compounds of the present invention.
[00024] Non-limiting examples of optional additives include adhesion promoters; biocides (antibacterials, fungicides, and mildewcides), anti-fogging agents; anti-static agents; bonding, blowing and foaming agents; dispersants; fillers and extenders; fire and flame retardants and smoke suppresants; impact modifiers; initiators; lubricants; micas; pigments, colorants and dyes;
plasticizers; processing aids; release agents; silanes, titanates and zirconates; slip and anti-blocking agents; stabilizers; stearates; ultraviolet light absorbers; viscosity regulators; waxes; and combinations of them.
[00025] Masterbatch Production
[00026] It has been found that it is possible to load a high percentage of fly ash and/or cinders into a carrier plastic resin to make a masterbatch.
Consequently, it is possible for the fly ash and/or cinders to be prepared into the form of a masterbatch with weight percent of the fly ash and/or cinders being at least 50 percent, desirably from about 72 to about 90 percent, and preferably from about 75 to about 85 percent by weight of the masterbatch. Indeed, the weight percent of fly ash and/or cinders desirably can be any percentage between 72 and 90 percent, stated in any range of two percents within that range. The carrier for the fly ash and/or cinders in the form of a masterbatch can be any plastic resin which is compatible with the plastic resin into which the masterbatch will be added, including any of the thermoplastic polymers identified above. Currently, linear low density polyethylene (LLDPE) or medium density polyethylene (MDPE) are identified as suitable carriers to make a masterbatch for use with polyolefin resins of the final thermoplastic compound.
[00027] Optionally, any of the additives identified above can be added to the masterbatch for later melt mixing with the plastic resin and other ingredients to be used to make the final plastic compound, whether molded, extruded, or calendered.
[00028] One can form the masterbatch using continuous or batch techniques, using extruders or mixers, respectively. Regardless of the manner of production, one having ordinary skill in the art should recognize that precautions may need to be taken against unnecessary wear of the equipment caused by the ceramic nature of the fly ash and/or cinders. Specialized surfaces can be used in those parts of the equipment against the fly ash and/or cinders particulate contacts when making the masterbatch. It has been found that once into the form of a masterbatch, the possibility of undue wear and tear on production molding or extruding equipment can be reduced, placing the care of equipment more upon the processor of the masterbatch and less on the purchaser of the masterbatch for subsequent compounding and final article formation.
[00029] The preparation of compounded pellets of fully let-down compound is explained in U.S. Pat. No. 7,879,939 (Prince et al.). The techniques described in Prince et al. can be used with fly ash and/or cinders in higher concentrations, in order to make the masterbatch.
[00030] Alternatively to what is explained in Prince et al., mixing in a continuous process typically occurs in an extruder that is elevated to a temperature that is sufficient to melt the polymer matrix with addition either at the head of the extruder or downstream in the extruder of the solid ingredient additives. Extruder speeds can range from about 50 to about 500 revolutions per minute (rpm), and preferably from about 100 to about 300 rpm. Typically, the output from the extruder is pelletized for later extrusion, molding, or calendering into polymeric articles.
[00031] Alternatively to what is explained in Prince et al., mixing in a batch process typically occurs in a Banbury or other batch mixer that is also elevated to a temperature that is sufficient to melt the polymer matrix to permit addition of the solid ingredient additives. The mixing speeds range from 60 to 1000 rpm. Also, the output from the mixer is chopped into smaller sizes for later extrusion, molding, or calendering into polymeric articles.
[00032] Masterbatches of carrier resin and fly ash and/or cinders can be purchased from PolyOne Corporation, as a distributor of Revolutionary Plastics, under the brand of Nano P.E.A.™ nano-sized polymer enhancing agent.
[00033] Commercial grades of these masterbatches can have from about
73 to about 85 weight percent of fly ash and/or cinders to the weight of the masterbatch, desirably 74 to 81 weight percent, and preferably 75 to 80 weight percent. The melt flow rate can range from about 5 to about 9 and preferably from about 5 to about 7 g/10 min. Moisture can range from about 100 to about 1000 ppm. The specific gravity can range from about 1.6 to about 1.8 and preferably from about 1.74 to about 1.78. The masterbatches are typically cut into pellets in a diameter of from about 2.5 mm to about 3.8 mm. A presently preferred grade of Nano P.E.A. is LLH7506 concentrate, which uses about 25 weight percent MDPE as a carrier and has about 75 weight percent of fly ash and cinders.
[00034] Subsequent Processing
[00035] Let-down of the masterbatch of the invention into a plastic resin during subsequent steps of reshaping by extrusion, molding, or calendering depends on the amount of functional filler desired by a person having ordinary skill in the art, without undue experimentation. Processing begins with melt- mixing the masterbatch with the plastic resin followed by reshaping by extrusion, molding, or calendering, followed by natural or accelerated cooling to form the final plastic article desired.
[00036] In the case of molding, particularly injection molding, the reshaping step includes pressurized injecting, holding, and cooling steps before the plastic article is ejected, the cycle of which the time is being measured to determine cycle time. More specifically, the reshaping step comprises four substeps of (1) injecting the compound into a mold; (2) holding the compound in the mold to form the plastic article in the shape of the mold; (3) cooling the plastic article to permit the plastic article to be released from the mold while retaining shape of the mold; and (4) ejecting the plastic article. The time between commencement of the injecting substep (1) and commencement of the ejecting substep (4) is one cycle time, and the cycle time of the compound is reduced from about 5 percent to about 30 percent for a plastic article of the compound as compared with a cycle time between commencement of substep (1) and commencement substep (4) for a plastic article that only contains the plastic resin without the masterbatch present.
[00037] Depending on whether the plastic compound into which the masterbatch is let down is a final plastic article or a core section of the final plastic article, the amount of masterbatch can vary. The desire for reduction of cycle time may need to be balanced the desire for a particular surface appearance of the final plastic article. Therefore, generally, the amount of masterbatch in the final polymer compound can range from about 1 to about 65 and preferably from about 20 to about 40 weight percent. As such, the weight percent of the fly ash and/or cinders functional filler in the final polymer compound can range from about 1 to about 58, desirably from about 5 to about 44, and preferably from about 10 to about 32 weight percent.
[00038] Subsequent extrusion or molding techniques are well known to those skilled in the art of thermoplastics polymer engineering. Without undue experimentation but with such references as "Extrusion, The Definitive Processing Guide and Handbook"; "Handbook of Molded Part Shrinkage and Warpage"; "Specialized Molding Techniques"; "Rotational Molding
Technology"; and "Handbook of Mold, Tool and Die Repair Welding", all published by Plastics Design Library (www.williamandrew.com), one can make articles of any conceivable shape and appearance using compounds of the present invention.
USEFULNESS OF THE INVENTION
[00039] Masterbatches of the present invention mixed with thermoplastic resin can be molded, extruded, or calendered with surprising efficiency and result in plastic articles having excellent physical properties and appearance.
[00040] It is possible that molding cycle times can be reduced by from about 5 percent to about 30 percent and preferably at least about 14 percent merely because of the presence of the fly ash and/or cinders as functional fillers, all other factors being equal.
[00041] Moreover, it has been found that comparable physical properties to a more expensive mineral-filled polyamide compound can be obtained with a less expensive fly ash- and/or cinders -filled polypropylene compound.
[00042] The fly ash and/or cinders functional filler can replace as much as about 65% of the plastic resin without unacceptable loss of physical properties. With the cost of the fly ash and/or cinders possibly being less than the cost of the plastic resin being replaced, less expensive molded, extruded, or calendered plastic articles can be made, without unacceptable loss of physical properties or sacrifice of ultimate surface appearance.
[00043] Any number of plastic articles can be benefit from the use of fly ash and/or cinders in the preparation of the polymer compound. Non-limiting examples of final plastic articles which can benefit from the invention include appliances (refrigerators, freezers, washers, dryers, toasters, blenders, vacuum cleaners, coffee makers, mixers); building and construction articles (fences, decks and rails, floors, floor covering, pipes and fittings, siding, trim, windows, window shutters, doors, molding, plumbing products, toilet seats, and wall coverings); consumer goods (power hand tools, rakes, shovels, lawn mowers, shoes, boots, golf clubs, fishing poles, and watercraft); electrical/electronic (printers, computer housings, business equipment, LCD projectors, mobile phones, connectors, chip trays, circuit breakers, and plugs); healthcare products (wheelchairs, beds, testing equipment, and packaging); industrial products (containers, bottles, drums, material handling, gears, bearings, gaskets and seals, valves, wind turbines, and safety equipment); packaging (food and beverage, cosmetic, detergents and cleaners, personal care, pharmaceutical and wellness); and transportation articles (automotive aftermarket parts, bumpers, window seals, instrument panels, consoles, under hood electrical, and engine covers).
[00044] A preferred means of using masterbatches of the invention is to have them introduced into the core sections of an extruded or molded article. For example, Prince et al. identified above describes how a fly-ash- and/or cinders-containing compound can be used in an extruded core section, which is full enclosed by a protective cladding, by manufacture using a co-extruder, to make a window shutter frame, louvers, or stiles or other elongated articles. Example 1 below proves successful injection molding of a core section.
EXAMPLES
[00045] Comparative Example A
[00046] A commercially available plastic article was molded in a two component mold having a core section of regrind/recycled polyolefins ( a mixture of polypropylene and polyethylene resins) and other ingredients comprising 40 weight percent of the article and a capstock section of prime polypropylene, enveloping the core section, comprising 60 weight percent of the article. The injection molding machine was operated in accordance with standard operating conditions for the molding of that particular style and shape of that plastic article. The applicable cycle time measured from commencement of the injecting step to commencement of the ejecting step was 116.5 seconds.
[00047] Example 1 [00048] The same plastic article was molded in the same injection molding machine operated in accordance with the same operating conditions with the same capstock section but with a core section comprising 37 weight percent of a masterbatch of LLH 7506 Nano P.E.A.™ polymer enhancing agent from Revolutionary Plastics LLC and the remaining 63 weight percent of the same regrind/recycled polyolefins and the other ingredients as contained in the core section of Comparative Example A. Overall, the masterbatch comprised 14.8% of the entire plastic article. The applicable cycle time measured was 99.5 seconds, a startling 14.59 percent improvement over the cycle time of
Comparative Example A.
[00049] The properties and appearance of the Example 1 plastic article were determined by the molder to be acceptable for commercial production and sale. In other words, to a skilled observer, no change in appearance or end-use properties was noticeable.
[00050] Achieving 14% reduction in cycle time is a major advantage for the molder over the competition still making the plastic articles according to the composition of Comparative Example A.
[00051] Considering the 14% improvement of applicable cycle time of
Example 1 over Comparative Example A, over only 24 hours, 127 more plastic articles could be made, all other factors being equal. That greater productivity extrapolates into 889 more plastic articles per week, 3,810 per 30-day month, and 46,355 more per year.
[00052] In a commercial world where time is money and commercial production requires continuous improvement to remain competitive in a global economy, any reduction in cycle time without loss of physical properties is tremendous advantage to the molder who uses the masterbatch of the present invention containing functional filler of fly ash and/or cinders. Almost 15% of cycle time improvement is gigantic.
[00053] The invention is not limited to the above embodiments. The claims follow.

Claims

What is claimed is:
1. A masterbatch for thermoplastic compounds of a first thermoplastic resin, comprising:
(a) fly ash and/or cinders and
(b) a second thermoplastic resin, compatible with or the same as the first thermoplastic resin, to serve as a carrier for the fly ash and/or cinders, wherein the fly ash and/or cinders comprises at least 50 percent by weight of the masterbatch.
2. The masterbatch of Claim 1, wherein the first thermoplastic resin and the second thermoplastic resin are selected from the group consisting of polyolefins, polyamides, polyesters, poly (meth)acrylates, polycarbonates, poly(vinyl halides), polyvinyl alcohols, polynitriles, polyacetals, polyimides, polyarylketones, polyetherketones, polyhydroxyalkanoates, polycaprolactones, polystyrenes, polyurethanes, polysulfones, polyphenylene oxides,
polyphenylene sulfides, polyacetates, liquid crystal polymers, fluoropolymers, ionomeric polymers, and copolymers of any of them and combinations of any two or more of them.
3. The masterbatch of Claim 1 or Claim 2, wherein the fly ash and/or cinders has a melting point or greater than about 1090°C; a specific gravity of from about 2.2 to about 2.8; less than 100 parts per million of lead, hexavalent chromium, mercury or cadmium, a moisture content of 1% or less; a polycyclic aromatic hydrocarbon content of less than about 200 parts per million; a crystalline silica content of below about 0.5%; and a particle size range in which about 85% of the particles fall within 0.2 μιη - 280 μιη, and remainder are less than about 850 μιη.
4. The masterbatch of any of Claims 1-3, wherein the masterbatch further comprises adhesion promoters; biocides, anti-fogging agents; anti-static agents; bonding, blowing and foaming agents; dispersants; fillers and extenders; fire and flame retardants and smoke suppresants; impact modifiers; initiators;
lubricants; micas; pigments, colorants and dyes; plasticizers; processing aids; release agents; silanes, titanates and zirconates; slip and anti-blocking agents; stabilizers; stearates; ultraviolet light absorbers; viscosity regulators; or waxes; or combinations of them.
5. The masterbatch of Claim 1 or Claim 2, wherein the fly ash and/or cinders comprises from about 72 to about 90 weight percent of the masterbatch.
6. The masterbatch of Claim 3, wherein the fly ash and/or cinders comprises from about 72 to about 90 weight percent of the masterbatch.
7. The masterbatch of any of the above Claims mixed with the first thermoplastic resin to form a thermoplastic compound.
8. A compound comprising the masterbatch of any of Claims 1-6 and the first thermoplastic resin.
9. The compound of Claim 8, in the shape of a molded plastic article, an extruded plastic article, or a calendered plastic article.
10. A method of using the masterbatch of any of Claims 1-6, comprising the steps of:
(a) melt-mixing the masterbatch and the first thermoplastic resin reshaping by extrusion, molding, or calendering a mixture of; and
(b) reshaping the compound to form a plastic article,
wherein the masterbatch has a weight percent in the plastic article ranging from about 1 to about 65 weight percent, and wherein the fly ash and/or cinders has a weight percent in the plastic article ranging from about 1 to about 58 weight percent.
11. The method of Claim 10, wherein the reshaping step comprises four substeps of:
(1) injecting the compound into a mold;
(2) holding the compound in the mold to form the plastic article in the shape of the mold;
(3) cooling the plastic article to permit the plastic article to be released from the mold while retaining shape of the mold; and
(4) ejecting the plastic article,
wherein time between commencement of the injecting substep (1) and commencement of the ejecting substep (4) is one cycle time, and
wherein the cycle time of the compound is reduced from about 5 percent to about 30 percent for a plastic article of the compound as compared with a cycle time between commencement of substep (1) and commencement of substep (4) for a plastic article of the first thermoplastic resin.
12. The method of Claim 11, wherein the first thermoplastic resin comprises polyethylene and the second thermoplastic resin comprises polyethylene, and wherein the cycle time of the compound is about 14 percent faster than the cycle time of the first thermoplastic resin.
13. The method of Claim 11 or Claim 12, wherein the plastic article is a core section about which a capstock section is also molded.
14. A molded plastic article made by the method of any Claims 10-13.
15. An extruded plastic article made by the method of Claim 10. A calendered plastic article made by the method of Claim 10.
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