US20180361629A1 - Thermally Expandable Mandrel Sealers - Google Patents

Thermally Expandable Mandrel Sealers Download PDF

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Publication number
US20180361629A1
US20180361629A1 US16/114,809 US201816114809A US2018361629A1 US 20180361629 A1 US20180361629 A1 US 20180361629A1 US 201816114809 A US201816114809 A US 201816114809A US 2018361629 A1 US2018361629 A1 US 2018361629A1
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Prior art keywords
coating
mandrel
thermally expandable
composite
film
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US16/114,809
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Matt Wallen
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Classifications

    • 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
    • B29C41/00Shaping by coating a mould, core or other substrate, i.e. by depositing material and stripping-off the shaped article; Apparatus therefor
    • B29C41/02Shaping by coating a mould, core or other substrate, i.e. by depositing material and stripping-off the shaped article; Apparatus therefor for making articles of definite length, i.e. discrete articles
    • B29C41/20Shaping by coating a mould, core or other substrate, i.e. by depositing material and stripping-off the shaped article; Apparatus therefor for making articles of definite length, i.e. discrete articles incorporating preformed parts or layers, e.g. moulding inserts or for coating articles
    • 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
    • B29C70/00Shaping composites, i.e. plastics material comprising reinforcements, fillers or preformed parts, e.g. inserts
    • B29C70/003Shaping composites, i.e. plastics material comprising reinforcements, fillers or preformed parts, e.g. inserts characterised by the matrix material, e.g. material composition or physical properties
    • 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
    • B29C33/00Moulds or cores; Details thereof or accessories therefor
    • B29C33/56Coatings, e.g. enameled or galvanised; Releasing, lubricating or separating agents
    • 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
    • B29C33/00Moulds or cores; Details thereof or accessories therefor
    • B29C33/56Coatings, e.g. enameled or galvanised; Releasing, lubricating or separating agents
    • B29C33/60Releasing, lubricating or separating agents
    • B29C33/62Releasing, lubricating or separating agents based on polymers or oligomers
    • 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
    • B29C35/00Heating, cooling or curing, e.g. crosslinking or vulcanising; Apparatus therefor
    • B29C35/02Heating or curing, e.g. crosslinking or vulcanizing during moulding, e.g. in a mould
    • 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
    • B29C41/00Shaping by coating a mould, core or other substrate, i.e. by depositing material and stripping-off the shaped article; Apparatus therefor
    • B29C41/02Shaping by coating a mould, core or other substrate, i.e. by depositing material and stripping-off the shaped article; Apparatus therefor for making articles of definite length, i.e. discrete articles
    • B29C41/025Shaping by coating a mould, core or other substrate, i.e. by depositing material and stripping-off the shaped article; Apparatus therefor for making articles of definite length, i.e. discrete articles having hollow walls
    • 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
    • B29C53/00Shaping by bending, folding, twisting, straightening or flattening; Apparatus therefor
    • B29C53/80Component parts, details or accessories; Auxiliary operations
    • B29C53/82Cores or mandrels
    • 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
    • B29C53/00Shaping by bending, folding, twisting, straightening or flattening; Apparatus therefor
    • B29C53/80Component parts, details or accessories; Auxiliary operations
    • B29C53/82Cores or mandrels
    • B29C53/821Mandrels especially adapted for winding and joining
    • B29C53/824Mandrels especially adapted for winding and joining collapsible, e.g. elastic or inflatable; with removable parts, e.g. for regular shaped, straight tubular articles
    • 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
    • B29C70/00Shaping composites, i.e. plastics material comprising reinforcements, fillers or preformed parts, e.g. inserts
    • B29C70/04Shaping composites, i.e. plastics material comprising reinforcements, fillers or preformed parts, e.g. inserts comprising reinforcements only, e.g. self-reinforcing plastics
    • B29C70/28Shaping operations therefor
    • B29C70/30Shaping by lay-up, i.e. applying fibres, tape or broadsheet on a mould, former or core; Shaping by spray-up, i.e. spraying of fibres on a mould, former or core
    • 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
    • B29C70/00Shaping composites, i.e. plastics material comprising reinforcements, fillers or preformed parts, e.g. inserts
    • B29C70/04Shaping composites, i.e. plastics material comprising reinforcements, fillers or preformed parts, e.g. inserts comprising reinforcements only, e.g. self-reinforcing plastics
    • B29C70/28Shaping operations therefor
    • B29C70/40Shaping or impregnating by compression not applied
    • B29C70/42Shaping or impregnating by compression not applied for producing articles of definite length, i.e. discrete articles
    • B29C70/46Shaping or impregnating by compression not applied for producing articles of definite length, i.e. discrete articles using matched moulds, e.g. for deforming sheet moulding compounds [SMC] or prepregs
    • B29C70/462Moulding structures having an axis of symmetry or at least one channel, e.g. tubular structures, frames
    • 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
    • B29C41/00Shaping by coating a mould, core or other substrate, i.e. by depositing material and stripping-off the shaped article; Apparatus therefor
    • B29C41/003Shaping by coating a mould, core or other substrate, i.e. by depositing material and stripping-off the shaped article; Apparatus therefor characterised by the choice of material
    • 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
    • B29C41/00Shaping by coating a mould, core or other substrate, i.e. by depositing material and stripping-off the shaped article; Apparatus therefor
    • B29C41/02Shaping by coating a mould, core or other substrate, i.e. by depositing material and stripping-off the shaped article; Apparatus therefor for making articles of definite length, i.e. discrete articles
    • B29C41/08Coating a former, core or other substrate by spraying or fluidisation, e.g. spraying powder
    • 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
    • B29C41/00Shaping by coating a mould, core or other substrate, i.e. by depositing material and stripping-off the shaped article; Apparatus therefor
    • B29C41/02Shaping by coating a mould, core or other substrate, i.e. by depositing material and stripping-off the shaped article; Apparatus therefor for making articles of definite length, i.e. discrete articles
    • B29C41/14Dipping a core
    • 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
    • B29C70/00Shaping composites, i.e. plastics material comprising reinforcements, fillers or preformed parts, e.g. inserts
    • B29C70/04Shaping composites, i.e. plastics material comprising reinforcements, fillers or preformed parts, e.g. inserts comprising reinforcements only, e.g. self-reinforcing plastics
    • B29C70/28Shaping operations therefor
    • B29C70/30Shaping by lay-up, i.e. applying fibres, tape or broadsheet on a mould, former or core; Shaping by spray-up, i.e. spraying of fibres on a mould, former or core
    • B29C70/34Shaping by lay-up, i.e. applying fibres, tape or broadsheet on a mould, former or core; Shaping by spray-up, i.e. spraying of fibres on a mould, former or core and shaping or impregnating by compression, i.e. combined with compressing after the lay-up operation
    • B29C70/345Shaping by lay-up, i.e. applying fibres, tape or broadsheet on a mould, former or core; Shaping by spray-up, i.e. spraying of fibres on a mould, former or core and shaping or impregnating by compression, i.e. combined with compressing after the lay-up operation using matched moulds
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B29WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29KINDEXING SCHEME ASSOCIATED WITH SUBCLASSES B29B, B29C OR B29D, RELATING TO MOULDING MATERIALS OR TO MATERIALS FOR MOULDS, REINFORCEMENTS, FILLERS OR PREFORMED PARTS, e.g. INSERTS
    • B29K2011/00Use of rubber derived from chloroprene as moulding material
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B29WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29KINDEXING SCHEME ASSOCIATED WITH SUBCLASSES B29B, B29C OR B29D, RELATING TO MOULDING MATERIALS OR TO MATERIALS FOR MOULDS, REINFORCEMENTS, FILLERS OR PREFORMED PARTS, e.g. INSERTS
    • B29K2027/00Use of polyvinylhalogenides or derivatives thereof as moulding material
    • B29K2027/12Use of polyvinylhalogenides or derivatives thereof as moulding material containing fluorine
    • B29K2027/18PTFE, i.e. polytetrafluorethene, e.g. ePTFE, i.e. expanded polytetrafluorethene
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B29WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29KINDEXING SCHEME ASSOCIATED WITH SUBCLASSES B29B, B29C OR B29D, RELATING TO MOULDING MATERIALS OR TO MATERIALS FOR MOULDS, REINFORCEMENTS, FILLERS OR PREFORMED PARTS, e.g. INSERTS
    • B29K2086/00Use of specific polymers obtained by polycondensation or polyaddition, not provided for in a single one of main groups B29K2059/00 - B29K2085/00, as moulding material
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B29WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29KINDEXING SCHEME ASSOCIATED WITH SUBCLASSES B29B, B29C OR B29D, RELATING TO MOULDING MATERIALS OR TO MATERIALS FOR MOULDS, REINFORCEMENTS, FILLERS OR PREFORMED PARTS, e.g. INSERTS
    • B29K2839/00Use of polymers with unsaturated aliphatic radicals and with a nitrogen or a heterocyclic ring containing nitrogen in a side chain or derivatives thereof, as mould material
    • B29K2839/06Polymers of N-vinyl-pyrrolidones
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B29WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29LINDEXING SCHEME ASSOCIATED WITH SUBCLASS B29C, RELATING TO PARTICULAR ARTICLES
    • B29L2009/00Layered products
    • B29L2009/005Layered products coated

Definitions

  • Composite plastic parts are of great value in industry because of their high strength and light weight. Tubular, simple, and complex structures are produced by laying on, wrapping, or coating a core mold, or mandrel, with the composite plastic and curing the composite at appropriately high temperature.
  • Core molds or mandrels, have been made with sand and binders, plaster, plaster mixed with various binders, fillers such as cenospheres or graphite, and other materials.
  • sealers applied to the mandrel prior to coating or wrapping the mandrel with raw composite plastic are easily removable from the cured composite product and produce higher quality composite products. Further, the utilization of expandable coating as sealer reduces the time and energy required for the curing process. The effective materials of such sealers are applied to a mandrel directly as a coating or as a film or tape.
  • Neoprene-based coating overcomes the difficulties and disadvantages of currently used coatings.
  • This coating can be applied to a mandrel as a spray or dip.
  • PTFE polytetrafluoroethylene
  • Adding an effective amount of polyvinylpyrrolidone, for example KV30-PVP, to neoprene creates a hardened surface for the coating when dehydrated. This coating is completely removable from the cured composite plastic product with water.
  • neoprene with PTFE Laurel Products Ultraflon ad10 is added to Chemionics dippable neoprene at about 30% by weight. This mixture is sprayed or the mandrel is dipped to coat the mandrel.
  • PVP K-30 is dispersed into a 30% by weight solution in water and Chemionics dippable neoprene is added at a ratio of 30 grams neoprene to 70 grams of the PVP K-30 solution. This mixture is sprayed on the mandrel and dehydrated or cured. Other molecular weights of PVP can be used, but much higher molecular weight PVP increases the viscosity so it is difficult to spray, but can be used to dip.
  • Composite material is then laid on, wrapped, or coated on the mandrel. The composite is cured in a way appropriate to the composite and the mandrel and coating are easily removed from the finished composite product.
  • a thermally expandable coating on a mandrel can be used in combination with a closed external mold. This is an internal thermally-induced pressurized system.
  • the expansion temperature is that temperature at which the utilized thermally-expandable component in the coating, sealer, film, or tape expands.
  • Azkonobel Expancel DU031 is mixed with PVP K-30 30% solution.
  • Expancel is dispersed into a liquid solution using a surfactant such as Surfynol 485 in the range of about 1-6% surfactant to 50% by weight Expancel in water.
  • This dispersed expansion media is then mixed into the 30% PVP K30 solution at about 1-10% PVP solution to 90-99% Expancel dispersion.
  • This mixed coating is applied to a mandrel.
  • the coating is dehydrated at less than 65° C. so as not to activate the expansion coating.
  • the dehydrated coating is then coated with a flexible coating such as base neoprene or other flexible coating and cured again at low temperature, if needed.
  • the part is then coated or wrapped with raw composite plastic and placed into a closed external mold. This is then heated above the expansion temperature and to appropriate curing conditions for the composite plastic. The thermally-induced expansion of the coating presses outward from the mandrel surface forcing the uncured composite onto the inner surface of the outer mold cavity. After taking the shape of the mold and curing, the composite and tool are all brought to room temperature and the part is ready to be removed from the mold. The entire part (mandrel and composite) is placed into a bath for disintegrating the mandrel. After removing the mandrel the neoprene is simply pulled from the composite producing a hollow continuous fiber, high tolerance article.
  • This method eliminates the necessity for an autoclave, vacuum pumps, bagging materials, release, breather, and also reduces scrap rate as the many of outer bag cured parts, using prior technology, are scrapped due to wrinkle formation or composite movement during vacuum autoclave curing.
  • This technique is good over a range of temperatures that can be tuned to the necessary pressurization curve and temperature defined by the composite system by selecting different grades of Expancel utilized at an effective concentration. Temperature ranges covered by this technique are from 70° C. to 220° C. cure cycles.
  • thermally expandable graphite is utilized at an effective concentration.
  • intercalated graphite expands by separating individual layers of graphite from the bulk graphite flake resulting in a significant volumetric expansion and therefore pressure exertion on any surrounding material, much like the Expancel material utilized in the above embodiment.
  • the invention relates to utilizing expandable graphite (such as Asbury Carbon) dispersed into aqueous solution near 50% with 1-10% surfactant to produce dispersed graphite.
  • any of several binders can be utilized, from PVP to methacrylates to neoprene for lower temperature applications, and polyimide, Kapton, silicone, or rubber can be used for higher temperature, or even soluble silicates can be used.
  • PVP polyvinyl acrylate
  • Kapton polyimide
  • silicone silicone
  • rubber can be used for higher temperature, or even soluble silicates can be used.
  • the majority of the binder ultimately will be destroyed upon heating to such high temperatures, but will allow the coating to survive the layup process, etc. before expanding.
  • the expandable graphite is mixed with a high temperature matrix such as silicone to produce a flexible film that can be applied to any surface that needs to exert pressure from the expansion of the film during thermally processing.
  • a high temperature matrix such as silicone
  • the film with contained expandable graphite is able to increase in size upon the application of sufficient heat.
  • the film can be produced as a controlled thickness film with or without adhesive.
  • the mandrel is subsequently wrapped or coated with raw composite plastic and placed into a closed external mold.
  • the assembly is heated above the expansion temperature of the utilized expandable graphite and cured appropriate to conditions needed to cure the composite.
  • pre-fabricated films or tapes can also be produced and utilized by applying/laying up onto to the mandrel prior to the composite layup.
  • These films/tapes are equally thermally activated like the spray-on/dipped coatings and apply, therefore, similar pressure on the laid up composite matrix when heated.
  • the films are produced by utilization of different carriers such as PTFE, Silicon, PVA, neoprene, latex or others to hold the desired effective charge of expandable materials.
  • Expandable materials can range from low temperature (up to 400° F.) activated to high temperature (over 800° F.) activated materials.

Abstract

It is sometimes advantageous to coat or seal the mandrel before laying on, coating, or wrapping the mandrel with composite plastic material. This invention provides improved coating with improved function that is easily removable from the cured product. The effective coating materials are applied directly to the mandrel as a coat or as a film or tape. Thermally expandable coat or film also reduces manufacturing costs for composite plastic products.

Description

  • This is a divisional of U.S. patent application Ser. No. 14/716,855, filed May 19, 2015.
  • RELATED APPLICATIONS
  • This application claims the benefits of U.S. Provisional Application 62/001,034, filed May 20, 2014.
  • BACKGROUND OF THE INVENTION
  • Composite plastic parts are of great value in industry because of their high strength and light weight. Tubular, simple, and complex structures are produced by laying on, wrapping, or coating a core mold, or mandrel, with the composite plastic and curing the composite at appropriately high temperature.
  • Multiple problems arise, however, in creating a core mold of sufficient strength, appropriate surface characteristics, compatibility with the composite and the curing process, and ease of removing the core from the cured composite structure without damage to the composite or significant additional cost.
  • Core molds, or mandrels, have been made with sand and binders, plaster, plaster mixed with various binders, fillers such as cenospheres or graphite, and other materials.
  • It is sometimes advantageous to apply a coating or sealer on the mandrel prior to laying on, coating, or wrapping the mandrel with the raw composite material. However, there are problems with currently used coatings, including their becoming brittle and/or difficult to remove completely from the cured product.
  • SUMMARY OF THE INVENTION
  • Improved sealers applied to the mandrel prior to coating or wrapping the mandrel with raw composite plastic are easily removable from the cured composite product and produce higher quality composite products. Further, the utilization of expandable coating as sealer reduces the time and energy required for the curing process. The effective materials of such sealers are applied to a mandrel directly as a coating or as a film or tape.
  • Applying the easily removable sealer, coating, film, or tape to an easily removable mandrel for the manufacture of a composite product results in a superior product from which the mandrel and sealer are easily removed, as described herein.
  • DESCRIPTION OF THE INVENTION Neoprene-Based Mandrel Sealing System
  • Neoprene-based coating overcomes the difficulties and disadvantages of currently used coatings. This coating can be applied to a mandrel as a spray or dip. The addition of an effective amount of polytetrafluoroethylene (PTFE) to neoprene, followed by curing, creates a self-releasing surface of the coating. Adding an effective amount of polyvinylpyrrolidone, for example KV30-PVP, to neoprene creates a hardened surface for the coating when dehydrated. This coating is completely removable from the cured composite plastic product with water.
  • All examples are for illustration and not intended to be limiting.
  • As an example of neoprene with PTFE, Laurel Products Ultraflon ad10 is added to Chemionics dippable neoprene at about 30% by weight. This mixture is sprayed or the mandrel is dipped to coat the mandrel.
  • As an example of neoprene with polyvinylpyrrolidone (PVP), PVP K-30 is dispersed into a 30% by weight solution in water and Chemionics dippable neoprene is added at a ratio of 30 grams neoprene to 70 grams of the PVP K-30 solution. This mixture is sprayed on the mandrel and dehydrated or cured. Other molecular weights of PVP can be used, but much higher molecular weight PVP increases the viscosity so it is difficult to spray, but can be used to dip. Composite material is then laid on, wrapped, or coated on the mandrel. The composite is cured in a way appropriate to the composite and the mandrel and coating are easily removed from the finished composite product.
  • Thermally Expandable Coatings
  • A thermally expandable coating on a mandrel can be used in combination with a closed external mold. This is an internal thermally-induced pressurized system. The expansion temperature is that temperature at which the utilized thermally-expandable component in the coating, sealer, film, or tape expands.
  • As an example of thermally expandable coating, Azkonobel Expancel DU031 is mixed with PVP K-30 30% solution. Expancel is dispersed into a liquid solution using a surfactant such as Surfynol 485 in the range of about 1-6% surfactant to 50% by weight Expancel in water. This dispersed expansion media is then mixed into the 30% PVP K30 solution at about 1-10% PVP solution to 90-99% Expancel dispersion. This mixed coating is applied to a mandrel. The coating is dehydrated at less than 65° C. so as not to activate the expansion coating. The dehydrated coating is then coated with a flexible coating such as base neoprene or other flexible coating and cured again at low temperature, if needed. The part is then coated or wrapped with raw composite plastic and placed into a closed external mold. This is then heated above the expansion temperature and to appropriate curing conditions for the composite plastic. The thermally-induced expansion of the coating presses outward from the mandrel surface forcing the uncured composite onto the inner surface of the outer mold cavity. After taking the shape of the mold and curing, the composite and tool are all brought to room temperature and the part is ready to be removed from the mold. The entire part (mandrel and composite) is placed into a bath for disintegrating the mandrel. After removing the mandrel the neoprene is simply pulled from the composite producing a hollow continuous fiber, high tolerance article. This method eliminates the necessity for an autoclave, vacuum pumps, bagging materials, release, breather, and also reduces scrap rate as the many of outer bag cured parts, using prior technology, are scrapped due to wrinkle formation or composite movement during vacuum autoclave curing. This technique is good over a range of temperatures that can be tuned to the necessary pressurization curve and temperature defined by the composite system by selecting different grades of Expancel utilized at an effective concentration. Temperature ranges covered by this technique are from 70° C. to 220° C. cure cycles.
  • High Temperature Thermally Expandable Coating
  • In the same general embodiment of the above, Expancel-based expansion coating system, expansion in excess of 200° C. is difficult, and the pressure exertion duration is short or the material melts too fast to exert pressure. To overcome this limitation, thermally expandable graphite is utilized at an effective concentration. In particular, intercalated graphite expands by separating individual layers of graphite from the bulk graphite flake resulting in a significant volumetric expansion and therefore pressure exertion on any surrounding material, much like the Expancel material utilized in the above embodiment. The invention relates to utilizing expandable graphite (such as Asbury Carbon) dispersed into aqueous solution near 50% with 1-10% surfactant to produce dispersed graphite. To bind the graphite coating, any of several binders can be utilized, from PVP to methacrylates to neoprene for lower temperature applications, and polyimide, Kapton, silicone, or rubber can be used for higher temperature, or even soluble silicates can be used. The majority of the binder ultimately will be destroyed upon heating to such high temperatures, but will allow the coating to survive the layup process, etc. before expanding.
  • In another embodiment of the invention, the expandable graphite is mixed with a high temperature matrix such as silicone to produce a flexible film that can be applied to any surface that needs to exert pressure from the expansion of the film during thermally processing. Just as the coating discussed above is able to produce pressure upon exfoliation of the contained expandable graphite, the film with contained expandable graphite is able to increase in size upon the application of sufficient heat. The film can be produced as a controlled thickness film with or without adhesive.
  • The mandrel is subsequently wrapped or coated with raw composite plastic and placed into a closed external mold. The assembly is heated above the expansion temperature of the utilized expandable graphite and cured appropriate to conditions needed to cure the composite.
  • The advantage to the utilization of an expandable surface coating, as opposed to an expandable mandrel, is that all of these systems require the thermal energy utilized for expansion to originate from the outer mold and pass through the composite and ultimately either into the mandrel or in this case just into the mandrel coating. As the heat flux into the system defines the overall rate of the process, a reduction in the amount of energy needed to input into the system is directly a reduction in the amount of time for processing. As the coating is on the surface of the mandrel it will expand well before the material in the center of the insulating core of the mandrel and as such will significantly reduce the processing time and provides a great advantage.
  • Examples are intended to illustrate the invention and are not limiting.
  • Thermally Expandable Films/Tapes
  • As an alternative to applying direct spray-on or dip coatings onto the unsealed mandrel, pre-fabricated films or tapes can also be produced and utilized by applying/laying up onto to the mandrel prior to the composite layup. These films/tapes are equally thermally activated like the spray-on/dipped coatings and apply, therefore, similar pressure on the laid up composite matrix when heated. The films are produced by utilization of different carriers such as PTFE, Silicon, PVA, neoprene, latex or others to hold the desired effective charge of expandable materials. Expandable materials can range from low temperature (up to 400° F.) activated to high temperature (over 800° F.) activated materials.
  • Many other variations of this invention will be understood by those skilled in the art.

Claims (10)

What is claimed:
1. (canceled)
2. (canceled)
3. The method of manufacturing a composite product comprised of steps:
a. Coating a mandrel with a thermally expandable coating,
b. Further coating or wrapping said coated mandrel with raw composite plastic,
c. Placing said coated mandrel of step b into a closed external mold, and
d. Heating the resulting assembly of step c above the expansion temperature and curing the composite plastic.
4. The method of manufacturing a composite product comprised of steps:
a. Coating a mandrel with a thermally expandable coating or with a pre-fabricated expandable film/tape,
b. Further coating said mandrel with a flexible coating or pre-fabricated film/tape,
c. Coating or wrapping said coated mandrel of step b with raw composite plastic,
d. Placing said coated or wrapped mandrel of step c. into a closed external mold, and
e. Heating the resulting assembly of step d above the expansion temperature and curing the composite material.
5. The method of claim 3 wherein said thermally expandable coating contains a thermally expandable material selected from the group: expandable microspheres, thermally expandable graphite.
6. The method of claim 5 wherein said thermally expandable material is at a concentration of nearly or about 50 percent.
7. The method of claim 3 wherein said thermally expandable coating contains thermally expandable graphite.
8. The method of claim 7 wherein said thermally expandable graphite is at a concentration of nearly 50%.
9. The method of claim 5 wherein said thermally expandable coating is a prefabricated film/tape.
10. The method of claim 6 wherein said said thermally expandable material is in a prefabricated film/tape.
US16/114,809 2014-05-20 2018-08-28 Thermally Expandable Mandrel Sealers Abandoned US20180361629A1 (en)

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US20210308967A1 (en) * 2020-04-07 2021-10-07 Rohr, Inc. Hybrid mandrel for use in tooling methods and the manufacture of thrust reverser cascades and structures susceptible to trapped tooling
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WO2014070381A1 (en) * 2012-10-31 2014-05-08 The Boeing Company System and method for manufacturing monolithic structures using expanding internal tools

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NO167963C (en) * 1983-02-07 1992-01-02 Hercules Inc PROCEDURE FOR MANUFACTURING A ROCKET ENGINE HOUSE.
FR2663258B1 (en) * 1990-06-13 1992-09-25 Aerospatiale MANDREL FOR THE MANUFACTURE OF HOLLOW BODIES OF COMPOSITE MATERIAL AND MANUFACTURE OF SUCH HOLLOW BODIES USING SAID MANDREL.
US20140017558A1 (en) * 2012-07-16 2014-01-16 Nthdegree Technologies Worldwide Inc. Diatomaceous Ionic Gel Separation Layer for Energy Storage Devices and Printable Composition Therefor

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US20120228467A1 (en) * 2007-07-13 2012-09-13 Advanced Ceramic Manufacturing Aggregate-based mandrels for composite part production and composite part production methods
WO2014070381A1 (en) * 2012-10-31 2014-05-08 The Boeing Company System and method for manufacturing monolithic structures using expanding internal tools
US20150137424A1 (en) * 2012-10-31 2015-05-21 The Boeing Company System and method for manufacturing monolithic structures using expanding internal tools

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