CA2209563C - Extruded polymer foam and method - Google Patents

Extruded polymer foam and method Download PDF

Info

Publication number
CA2209563C
CA2209563C CA002209563A CA2209563A CA2209563C CA 2209563 C CA2209563 C CA 2209563C CA 002209563 A CA002209563 A CA 002209563A CA 2209563 A CA2209563 A CA 2209563A CA 2209563 C CA2209563 C CA 2209563C
Authority
CA
Canada
Prior art keywords
extruder
polyol
isocyanate
filler particles
foam
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.)
Expired - Fee Related
Application number
CA002209563A
Other languages
French (fr)
Other versions
CA2209563A1 (en
Inventor
James H. Burgess
Sammie J. Glorioso
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.)
IP Rights LLC
Original Assignee
Apache Building Products Co
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 Apache Building Products Co filed Critical Apache Building Products Co
Publication of CA2209563A1 publication Critical patent/CA2209563A1/en
Application granted granted Critical
Publication of CA2209563C publication Critical patent/CA2209563C/en
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

Links

Classifications

    • 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
    • C08J9/00Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof
    • C08J9/0066Use of inorganic compounding ingredients
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B29WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29BPREPARATION OR PRETREATMENT OF THE MATERIAL TO BE SHAPED; MAKING GRANULES OR PREFORMS; RECOVERY OF PLASTICS OR OTHER CONSTITUENTS OF WASTE MATERIAL CONTAINING PLASTICS
    • B29B7/00Mixing; Kneading
    • B29B7/30Mixing; Kneading continuous, with mechanical mixing or kneading devices
    • B29B7/58Component parts, details or accessories; Auxiliary operations
    • B29B7/60Component parts, details or accessories; Auxiliary operations for feeding, e.g. end guides for the incoming material
    • B29B7/603Component parts, details or accessories; Auxiliary operations for feeding, e.g. end guides for the incoming material in measured doses, e.g. proportioning of several materials
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B29WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29BPREPARATION OR PRETREATMENT OF THE MATERIAL TO BE SHAPED; MAKING GRANULES OR PREFORMS; RECOVERY OF PLASTICS OR OTHER CONSTITUENTS OF WASTE MATERIAL CONTAINING PLASTICS
    • B29B7/00Mixing; Kneading
    • B29B7/74Mixing; Kneading using other mixers or combinations of mixers, e.g. of dissimilar mixers ; Plant
    • B29B7/7476Systems, i.e. flow charts or diagrams; Plants
    • B29B7/748Plants
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B29WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29BPREPARATION OR PRETREATMENT OF THE MATERIAL TO BE SHAPED; MAKING GRANULES OR PREFORMS; RECOVERY OF PLASTICS OR OTHER CONSTITUENTS OF WASTE MATERIAL CONTAINING PLASTICS
    • B29B7/00Mixing; Kneading
    • B29B7/80Component parts, details or accessories; Auxiliary operations
    • B29B7/82Heating or cooling
    • B29B7/823Temperature control
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B29WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29BPREPARATION OR PRETREATMENT OF THE MATERIAL TO BE SHAPED; MAKING GRANULES OR PREFORMS; RECOVERY OF PLASTICS OR OTHER CONSTITUENTS OF WASTE MATERIAL CONTAINING PLASTICS
    • B29B7/00Mixing; Kneading
    • B29B7/80Component parts, details or accessories; Auxiliary operations
    • B29B7/82Heating or cooling
    • B29B7/826Apparatus therefor
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B29WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29BPREPARATION OR PRETREATMENT OF THE MATERIAL TO BE SHAPED; MAKING GRANULES OR PREFORMS; RECOVERY OF PLASTICS OR OTHER CONSTITUENTS OF WASTE MATERIAL CONTAINING PLASTICS
    • B29B7/00Mixing; Kneading
    • B29B7/80Component parts, details or accessories; Auxiliary operations
    • B29B7/88Adding charges, i.e. additives
    • B29B7/90Fillers or reinforcements, e.g. fibres
    • 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
    • B29C44/00Shaping by internal pressure generated in the material, e.g. swelling or foaming ; Producing porous or cellular expanded plastics articles
    • B29C44/34Auxiliary operations
    • B29C44/3442Mixing, kneading or conveying the foamable 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
    • B29C44/00Shaping by internal pressure generated in the material, e.g. swelling or foaming ; Producing porous or cellular expanded plastics articles
    • B29C44/34Auxiliary operations
    • B29C44/36Feeding the material to be shaped
    • B29C44/46Feeding the material to be shaped into an open space or onto moving surfaces, i.e. to make articles of indefinite length
    • B29C44/50Feeding the material to be shaped into an open space or onto moving surfaces, i.e. to make articles of indefinite length using pressure difference, e.g. by extrusion or by spraying
    • B29C44/505Feeding the material to be shaped into an open space or onto moving surfaces, i.e. to make articles of indefinite length using pressure difference, e.g. by extrusion or by spraying extruding the compound through a flat die
    • 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
    • C08J9/00Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof
    • C08J9/04Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof using blowing gases generated by a previously added blowing agent
    • C08J9/12Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof using blowing gases generated by a previously added blowing agent by a physical blowing agent
    • C08J9/14Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof using blowing gases generated by a previously added blowing agent by a physical blowing agent organic
    • C08J9/143Halogen containing compounds
    • C08J9/144Halogen containing compounds containing carbon, halogen and hydrogen only
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B29WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29BPREPARATION OR PRETREATMENT OF THE MATERIAL TO BE SHAPED; MAKING GRANULES OR PREFORMS; RECOVERY OF PLASTICS OR OTHER CONSTITUENTS OF WASTE MATERIAL CONTAINING PLASTICS
    • B29B7/00Mixing; Kneading
    • B29B7/30Mixing; Kneading continuous, with mechanical mixing or kneading devices
    • B29B7/34Mixing; Kneading continuous, with mechanical mixing or kneading devices with movable mixing or kneading devices
    • B29B7/38Mixing; Kneading continuous, with mechanical mixing or kneading devices with movable mixing or kneading devices rotary
    • B29B7/40Mixing; Kneading continuous, with mechanical mixing or kneading devices with movable mixing or kneading devices rotary with single shaft
    • B29B7/42Mixing; Kneading continuous, with mechanical mixing or kneading devices with movable mixing or kneading devices rotary with single shaft with screw or helix
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B29WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29BPREPARATION OR PRETREATMENT OF THE MATERIAL TO BE SHAPED; MAKING GRANULES OR PREFORMS; RECOVERY OF PLASTICS OR OTHER CONSTITUENTS OF WASTE MATERIAL CONTAINING PLASTICS
    • B29B7/00Mixing; Kneading
    • B29B7/30Mixing; Kneading continuous, with mechanical mixing or kneading devices
    • B29B7/34Mixing; Kneading continuous, with mechanical mixing or kneading devices with movable mixing or kneading devices
    • B29B7/38Mixing; Kneading continuous, with mechanical mixing or kneading devices with movable mixing or kneading devices rotary
    • B29B7/46Mixing; Kneading continuous, with mechanical mixing or kneading devices with movable mixing or kneading devices rotary with more than one shaft
    • B29B7/48Mixing; Kneading continuous, with mechanical mixing or kneading devices with movable mixing or kneading devices rotary with more than one shaft with intermeshing devices, e.g. screws
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B29WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29BPREPARATION OR PRETREATMENT OF THE MATERIAL TO BE SHAPED; MAKING GRANULES OR PREFORMS; RECOVERY OF PLASTICS OR OTHER CONSTITUENTS OF WASTE MATERIAL CONTAINING PLASTICS
    • B29B7/00Mixing; Kneading
    • B29B7/74Mixing; Kneading using other mixers or combinations of mixers, e.g. of dissimilar mixers ; Plant
    • B29B7/7404Mixing devices specially adapted for foamable substances
    • 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
    • C08J2201/00Foams characterised by the foaming process
    • C08J2201/02Foams characterised by the foaming process characterised by mechanical pre- or post-treatments
    • C08J2201/03Extrusion of the foamable blend
    • 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
    • C08J2375/00Characterised by the use of polyureas or polyurethanes; Derivatives of such polymers
    • C08J2375/04Polyurethanes

Abstract

Process of extrusion of high levels of filler which is contained in a polyol and an isocyanate in a screw extruder (32) along with a catalyst, a surfactant and a blowing agent and the mixture is extruded to produce a thermoset onto a conveyor (2) and subsequently foamed.

Description

EXTRUDED POLYMER FOAM AND METHOD
Field Of The Inventian The invention relates to foamed polymer material, methods for producing polymer foams, and, particularly, to a method for extruding polymer foam material, such as poiyisocyanurate and polyurethane foams, using a screw-type extruder. The extruded polymer foams contain substantial amounts of filler particles.
Background Of The Invention Polymer foams, ~;uch as poly_socyanurate a::d polyurethane foams, have not previously been able to be produced using an extruder. The foaming material "firms" in the extruder and blocks the equipment. Additiona--ly, use of f,_ller materials has been limited using conventional methods to produce foam sheets.
U.5. Patent nio. 3,465,70, (Richie) describes an apparatus for extruding foamable thermoplastic material, such as polystyrene, preferably ir: tui:ular corm. Richie discloses that the apparatus c:an be used for thermosetting materials, such as polyurethanes, but that steam or hot water would have a damaging effect and therefore are not used. A foam-augmenting gas such as freon is used as the foaming agent.
Richie use an expansion space o~ transverse cross-sectional area which increases in size gradually in the direction of travel of the extruded product.
U.S. Patent No. 5,149,722 (Soukup) and U.S. Patent No.
4,795,763 (Gluck) describes the use of about 1-10% by weight of carbon black as a filler material. Gluck specifically recites the problem of cell rupture which can occur with the addition of too much filler materials.
Summary Of The Invention Polymer foam board is disclosed which preferably includes high levels of filler material, such as 15%-20% by weight filler particles, or higher. Polyisocyanurate or polyurethane foam is made using a screw-type extruder for l0 mixing the components of the composition. Isocyanate and polyol are introduced into a screw of an extruder. Filler particles are also preferably introduced in the extruder screw. The isocyanate, polyol, and filler particles (if employed) are mixed together with a foaming agent and, optionally, a surfactant with the extruder to produce a high quality dispersion. The mixture is cooled via a cooling manifold of the screw extruder and the addition of the various components in the mixture. Cooling inhibits reaction of the mixed components within the screw.
Catalyst is added and mixed with the polyol/isocyanate/filler particle mixture in the extruder screw as a final mixing step. After the catalyst is introduced, the mixture is almost immediately extruded onto a conveyor so that the firming occurs outside of the extruder to avoid clogging. The mixture is foamed and firmed on the conveyor in a conventional manner and, preferably, formed into a continuous flat sheet which is thereafter cut to produce boards of standard sizes.

WO 96120966 PCTlUS95/OOI75 The filler particles included in the thermoset foams produced in accordance with the invention maintain the mechanical or insulative characteristics of the resultant extruded foam as compared to the properties of the extruded foam without filler particles. However, with some fillers improved characteristics result. For example, carbon black can improve the insulation properties of the foam as set forth in the Soukup and Gluck patents, supra. Overall, the addition of filler particles make the resultant foam more economical to produce and the process enables the use of more filler materials in the production of suitable foam board insulation.
Different filler particles can be used in the same foam.
For example, carbon black and another type filler particle, which is less expensive, can be used to gain the insulative effect of the carbon black while increasing costs savings.
Aluminum trihydrate, perlite and calcium carbonate are preferred filler materials, used either as the sole filler material or with carbon black. Other filler materials include carbon black, diatomaceous earth, polyiso powder, and barium sulfate and calcium silicate. The filler particles added to the polyol/isocyanate mixture in the extruder reduce the cost of the resultant extruded thermoset foam, since the filler particles are lower in cost than polyol and/or polyisocyanate .
The filler particles and/or dispersant and/or foaming agent and/or surfactant may be mixed with the isocyanate or with the polyol before introduction thereof to the extruder screw. If multiple fillers are used, they can be mixed prior to entering the extruder screw or can be introduced, simultaneously.or separately, into the extruder screw and mixed therein. Entry of the filler particles, or a filler particle mixture can occur simultaneously or separately from entry of dispersing agent and/or surfactant and/or the polyol and/or the isocyanate.
The foaming agent, which is preferably a hydrochloro-fluorocarbon (HCFC) or water, is preferably introduced directly into the extruder or may be mixed with one of the components, preferably the polyol, before introduction thereof to the extruder screw. If water is the -foaming agent, the water is vaporized for foaming the mixture and reacts with the isocyanate to form carbon dioxide, which further foams the mixture. Other foaming agents may alternatively be used.
Foam cell size is generally decreased when extruder speed is increased.
A filler particle dispersion may be made in the extruder using filler particles, dispersant, optional surfactant, and isocyanate or polyol. Preferably, a catalyst is added to this dispersion for immediate extrusion and foaming. Alternatively the dispersion can be stored for future use. An extruder provides better quality dispersion, measuring 8 or more on the Hegman scale, than a dispersion made in a Kady (kinetic dispersion) mill. , It is an object of the invention to provide an improved method for making polymer foams containing filler particles. ' It is another obj ect of the invention to provide a method for extruding filler particle-containing thermosetting foams, -5_ such as polyisocyanurate and polyurethane foams, using a screw-type extruder, such as a twin-screw extruder.
It is yet another object of the invention to provide a method for making a filler particle dispersion in an extruder.
It is a further object of the invention to combine preparation of a filler particle dispersion and production of a foam using the filler particle dispersion, in a single operation.
It is a further object of the invention to provide a thermoset polymer foam formed by mixing polyol, foaming agent and isocyanate with a catalyst in an extruder and immediately extruding the reactants wherein the filler particles comprise at least 12% by weight of the thermoset polymer foam.
Brief Description Of The Drawings Figure 1 is a schematic illustration of an apparatus for extruding polymer foam onto a conveyor.
Figure 2 is a schematic illustration of an extruder for an integrated process including preparation of a polymer premix before extruding the polymer mixture for foaming.
Figure 3 is a cross-sectional view of a preferred extruder outlet.
Figure 4 is a front elevational view of the outlet shown in Figure 3.

-5a-Detailed Description Of The Invention Thermosetting foams, such as polyisocyanurate or polyurethane foams, are made using an extruder for mixing the foamable mixture before extruding onto a belt conveyor.
Through such a continuous process, thermosetting foams are made much faster than previously possible without any decrease in quality., Additionally, the process enables the dispersion of filler particles with the polymer mixture to produce foams which include 12-15o by weight or more filler particles thereby reducing the production cost of the thermoset foams.
The extruder enhances the dispersion of the polymer , mixture. A twin-screw extruder is preferred. However, a single screw extruder with multiple mixing sections can also be used. The extruder can process materials for making a thermosetting polymer, such as an isocyanate polymer, in a controlled manner with independent catalyst addition and variable reactivity. High quality filler particle dispersions in isocyanate or polyol media are obtained. These dispersions exceed 8 on the Hegman scale. Moreover, higher levels of filler particles can be handled than on conventional foam mixing equipment.
The foams may be blown with blowing agents such as hydro chlorofluorocarbons (HCFC), CFC, HFC, HC and/or water which produces CO2. Typical examples of hydrochlorofluorocarbon blowing agents are HCFC 141b and HCFC 22 which can be advantageously combined in preferred proportions. High viscosity isocyanates and polymer premix, which cannot be processed using a conventional Kady mill and conventional foam mixing equipment, may be used in the process described.
The extruder is cooled downstream of the dispersion section of the extruder to prevent premature reaction of the foam ingredient. The low torque requirements permit use of virtually any size extruder. Flocculation of filler particle/polyol dispersions can be avoided by maintaining a high shear rate on the dispersion, through the foaming section, producing a foam with excellent filler particle WO 96120966 PCTlL1S95/001~5 dispersion.

In general, the quality of the dispersion increases with increased filler particle loading and with viscosity of the starting medium. Addition of the polyol or isocyanate in the dispersion section may be accomplished in several staged injections. This is preferred for keeping the viscosity and shear high enough to ensure a high quality dispersion.

The preferred dispersions were obtained when the charge of filler particles was added with the first injection of the dispersion medium to form a mixture. The final preferred filler percentage of 12% to 20o was then obtained by subsequent liquid injections in the dispersion section of the extruder. Maximum temperatures of about 50C. in the dispersion section do not present an operational problem. The dispersion is actively cooled by cold water circulating in the barrel jackets and screws and passively cooled by injection of the remaining foam ingredients into the dispersion.

A preferred extruder screw speed to provide a good foam mix i s about 3 0 0 - 6 0 0 rpm . Speeds may range t o 10 0 0 rpm or higher. For extended use at high speed, a special hardening treatment is advantageously used on the screw element in the dispersion section due to the abrasiveness of the filler particles. Throughput is a function of both screw speed and extruder size. A desired throughput for a 30-40mm extruder is about 450-600 lb./hr.

One method of extruding polyisocyanurate foam includes adding a blend of isocyanate, and filler particles at a first position of the extruder, adding polyol blend to mix with the _g_ isocyanate blend at a second position of the extruder closer to the extrusion position than the first position, adding catalyst blend to the mixed polyol and isocyanate blend at a third position of the extruder proximate the extrusion position, and extruding the catalyzed mixture onto a belt conveyor for foaming.
With reference to Figure 1, an extruder apparatus 2 suitable for practicing the invention is illustrated. The apparatus 2 includes an extruder 4 which has barrels, B1-B9.
A single or twin screw extruder may be used. A twin screw extruder provides better mixing and is preferred. The barrels of the extruder are preferably separated by sheets of Graphoil paper, which aids in taking down the apparatus.
Isocyanate solution is mixed and provided to reservoir 6 having a large capacity, preferably a 30 gallon capacity.
A suspension of filler particles in the isocyanate may be fed to reservoir 6 or the filler particles can be fed into barrel Bl via a hopper 8. Solution from reservoir 6 is fed, in a non-limiting example, to barrel B7 of extruder 4. Polyol is mixed with water (foaming agent), for example in Lightning mixer 10, and fed to extruder 4 at location 12, between barrels B7 and B8. Alternatively, the isocyanate and the filler particles may be fed, for example, to hopper 8 feeding into barrel Bl, and the isocyanate and/or filler particles mixed together in the extruder before the polyol is added.
The polyol and isocyanate containing filler particles are ' mixed in the extruder. Thereafter catalyst is fed from a reservoir 14 to barrel B9 and mixed therewith. The catalyzed mixture is fed through the discharge end of the extruder onto a belt conveyor. The discharge end 16 of the extruder - suitably has an inclined discharge piece 18 or a flat discharge piece (Figure 4), for directing the foam downward onto a conveying/forming apparatus 11.
The temperature in the extruder is controlled by cooling the barrels and screws, as known in the art. Barrels B7 through B9 (at least) are cooled, generally by water cooling, to facilitate mixing the components of the reaction mixture without clogging the extruder.
The conveying/forming apparatus 11 includes a conveyor 20, onto which the foam is discharged from end 16 of extruder 2. The foam, passes between a pair of rolls 23 which rotate in opposite directions and then onto a slat conveyor 24, 26 through a heated area 28 in which the foam rises.
Optionally the foam is introduced between upper and lower paper liners. Appropriate location of the lining paper rolls (not shown) is apparent to one skilled in the art. The resultant product is a laminated insulation sheet.
Slat conveyors typically vary from 20-100 feet in length.
T L, ~ ~, l -, +- 7 d h o ~ +- o .a t r, ~ l-, r" , t ~ ~ n o ~ m ~, ; o r, ~
r t i r, r, 1116 .71Q4 conveyor 4Z 1s llccLV.cW .v cuJJVUL 1-JV 1 . .111.x..7 lrv.W .lvla of the conveyor is substantially closed in by enclosure 28 to conserve heat. Doors (not shown) are placed about every 10 ft . along the enclosure to allow access to the equipment . The mixture foams and firms as it passes at about 30 to 150 ' ft./min. along the conveyor. Thefoam passes onto a roller conveyor 30 about 20 to 100 ft. in length, substantially at room temperature, for curing before being cut into panels for use . A typical apparatus of this type is shown in Gluck, U. S .
Patent No. 4,795,763, discussed above.
In another example, shown in Figure 2, an extruder 32 _ having 12 barrels A1-A12 is used. Filler particles are fed to barrel Al from hopper 34, a premix of polyol and surfactant is fed from mixer 36 between barrels Al and A2 and mixed together with the filler particles in the extruder screw. The remainder of the polyol is added from a reservoir 38 to barrel A6 and mixed with the filler particle and polyol premix.
Isocyanate is fed from a reservoir 40 to barrel A9 and mixed with the ingredients already in the screw of the extruder.
In this example, hydro-chlorofluorocarbon blowing agent (HCFC-141b) is used, and is added from a reservoir 42 to barrel A11.
Catalyst, such as potassium octoate, is added from a reservoir 44 to barrel-A12 of the extruder, and mixed into the reaction mix immediately before extrusion. The mixture is extruded from die 46 onto a conveying/forming apparatus, such as illustrated in Figure 1_ Where more than one type of filler material is to be used, separate feed bins 48 for each type of material are provided . The amount of f filler fed to the hopper 34 f rom each bin is controlled to provide a desired proportion. A
preferred combination of filler materials is carbon black and aluminum trihydrate, relative proportions are dependent upon the R value and physical properties desired. For making dispersions without foaming, the fillers are added via hopper 34 and the isocyanate is added from mixer 36 and reservoir 38.
It is well known in the art of thermosetting foams that, in the process of making polyisocyanurate or polyurethane foams, when the mixture is prepared, there is an exothermic foaming reaction. The speed of this reaction is controllable according to the temperature at which the reaction takes place . The foaming action is described as having a "cream time," during which foaming is initiated and the material reaches a consistency of a soft creamy foam, and a "firm time"
at which the foam sets up and hardens. In a typical non-limiting example, the cream time may be 7 to 12 seconds and the firm time may be 35 to 60 - seconds . The properties of the product may be changed by adjusting the concentrations of the materials, temperatures of the barrels, etc.
In prior attempts to extrude thermosetting resins of this type, extrusion has not been successful because the reaction mechanism has not been controlled within the extruder and the mixture has creamed and/or foamed within the extruder and blocked the extruder, preventing extrusion.
A typical extruder die which is useful in avoiding . excessive build-up of foam on the die is shown in Figures 4 and 5. Discharge plate 50 of extruder 52 is attached to barrel 54. Screw 56 has a flat tip 58 and discharged material 60 falls directly between rolls 62,64 carrying lining paper 66, 68 for the conveyor (as shown in Figure 1) on which the isocyanate polymer is foamed.
In making insulation boards, the extrusion process described herein allows fast, economical production. Filler particle addition reduces the cost of the insulation boards so produced. The thermal conductivity of insulation board is R'O 96/20966 PCT/LTS95/00175 reduced by adding carbon black. This advantageously reduces board thickness. The thermal conductivity of polyisocyanurate foams, based on different foaming agents, in BTU per cu.ft., per hr., per °F, are as follows:
isocyanurate/HCFC 0.12 isocyanurate/carbon black/HCFC 0.09-0.1 isocyanurate/water 0.14-0.19 isocyanurate/carbon black/water 0.135-0.17 isocyanurate/carbon black/HCFC/water 0.09-0.135 Use of HCFC (hydrochlorofluorocarbon) foaming agent advantageously reduces the foam's thermal conductivity.
Carbon black also reduces the thermal conductivity, compensating for increased thermal conductivity when water is the foaming agent. The formulation may also include inorganic flame retardants. Inorganic flame retardants increase the isocyanurate and polyol components' viscosities. A screw extruder allows thorough mixing of higher. viscosity components with better dispersion for use of higher percentage of filler materials. The mix is discharged from the extruder prior to the start of the firming reaction.
A filler particle dispersion may be made in the extruder using the filler particles, carbon black, optional surfactant and isocyanate or polyol. Dispersi-ons may be used immediately or stored for future use. Isocyanate dispersions are preferred where storage is intended, since polyol dispersions tend to become less disperse when stored.

WO 96/20966 pcTirJS9siooi75 Examples 1 to 33 Carbon black dispersion made in the extruder screw Table 1 shows the composition used for each formulation and Table 2 shows the composition of each polyol premix, used as indicated in Table 1. Pelron P-344 dispersant and Cabot Black Pearls 280 carbon black were used in all the examples.
The catalyst was a 3:1 blend, by weight, of potassium octoate and DMP-30. A catalyst blend of 3:1 to 6:1 may be used. The ratio of the catalyst blend is dependent upon how close the catalyst is added to the extruder outlet. The average equivalent weight of BASF 226 prepolymer (polymerJisocyanate mix) and ICI high viscosity isocyanate is about 152.
The operating run schedule is shown in Table 3 and operating parameters of the extruder are shown in Table 4.
The torque developed was higher for the carbon black dispersions when compared with the white controls, but was still very low relative to the capabilities of the extruder, and is not a limiting factor. Exit temperatures of the foam mix are shown to be a function of the level of carbon black and the original viscosity of the dispersion medium. The preferred exit temperature is about 25° to 32°C.
Table 5 shows properties of selected test foams.
Example 34 Carbon black dispersion made outside the extruder screw Component A: Polymeric methyldiisocyanate (MDI) 91a carbon black 90 (viscosity: 20,000 cps) (dispersion quality: Hegman bar - 50 microns) Component B: polyol 91%
silicone surfactant 50 water 4%

Comt~onent C: preblended catalyst (potassium octoate) 2%

Components A, B and C were mixed in the percentage ratio A:B:C of 74:24:2, by weight.
Table 1 FormulationComponent Parts ~ Index by Trimer Weight I Premix I 40.6 11.8 2.74 12.4 2852E Polyol 59.4 17.2 MR-200 Isocyanate192.0 55.7 Catalyst 7.5 2.2 HCFC - 141b 45.0 13.1 II Premix II 40.6 11.2 2.93 12.8 Carbon Black 17.4 4.8 (C/B) 2852E Polyol 59.4 16.4 MR-200 Isocyanate192.0 53.0 Catalyst 7.5 2.1 HCFC - 141b 45.0 12.4 III Premix III 63.5 17.0 3.00 12.9 Carbon Black 27.2 7.3 (C/B) 2852E Polyol 36.5 9.8 MR-200 Isocyanate192.0 51.5 Catalyst 7.5 2.0 HCFC-141b 46.3 12.4 IV Premix IV 40.6 11.5 2.97 12.7 Carbon Black 17.4 4.9 (C/B) 2852E Polyol 50.0 14.2 Isocyanate (ICI,192.0 54.5 or BASF 226 Prepolymer) Catalyst 7.5 2.1 HCFC-141b 45.0 12.8 Table 2 Polyol Premix I II III IV

pbw % pbw % pbw % pbw %

2852E Polyol 37.1 91.4 33.9 83.5 55.0 86.6 33.9 83.5 Y10222 3.5 8.6 3.5 8.6 3.5 5.5 3.5 8.6 Surfactant P-344 Dispersant- - 3.2 7.9 5.0 7.9 3.2 7.9 Table 3 - RUN SCHEDULE
Run No. FormulationFoam Key Variable Type 1 5 1 I White Control Density Check 1.65 2 I White Control Lower 141b 1.67 3 I White Control Higher 141b 1.51 4 II Black Control Hegman 7 5 II Black Control Lower 141b 2 0 6 II Black Control ISO Adjustment 7 II Black Control Mix/Rate Study600RPM
~

8 II Black Control Mix/Rate Study500RPM
Q

9 II Black Control Mix/Rate Study600RPM
Q

10 III Black Control Mix/Rate Study600RPM
c~

2 5 11 III Black Control Mix/Rate Study500RPM
~

12 III Black Control Mix/Rate Study500RPM
C~

13, 13A IV Black,Prepol. Mix C~ 500 RPM, 13A Higher ISO

14 IV Black,Prepol. Mix C~ 600 RPM

15 IV Black,Prepol. Mix/Rate Study600RPM
@

3 0 16 IV Black,Prepol. Mix/Rate Study500RPM
~

17 IV Black,Prepol. Mix/Rate Study500RPM
Q

18 IV Black,ICI Mix Q 500 RPM

19 IV Black,ICI Mix Q 600 RPM

20 ' IV Black,ICI Catalyst Adjustment 3 5 21 IV Black,ICI 141b Adjustment 22 IV Black,ICI 141b Adjustment 23 IV White,Prepol. Control 24 IV Black,Prepol. Prepol + C/B

25 IV Black,Prepol. Higher C/B RPM
~ 500 4 0 26 IV Black,Prepol. Higher C/B RPM
Ca7 600 27 IV Black,Prepol. Low Rate, Low Matl.
on 28 IV White Control ICI High Visc.
ISO

29 IV Black Control Std. % C/B

30 IV Black Control Higher C/B
~

4 5 31 IV Black Control C/B
Higher 32 IV Black Control Higher C/B

33 IV TnThiteControl R-22 Froth SUBSTITUTf SHEET (RULE 26) Table 4 - OPERATING PARAMETERS
Run RPM ~ lbs/hr Exit ~ C/B Foam No. Torque Temp. Quality 'C

1 50D 5.1 300 28 0 Good 2 500 5 300 27 0 Good 3 500 4.9 300 28 0 Good 4 500 16 300 27 4.8 Good 500 15.9 300 28 4.8 Good 6 500 15.8 300 28 4.8 Good 7 600 15.2 300 29 4.8 Good 8 500 17.7 400 29 4.8 Good 9 600 16.4 4D0 29 4.8 Good 600 16.7 450 29 7.3 Good 11 500 22 450 29 7.3 Good 12 500 24 400 29 7.3 Good 13 500 14.3 300 30, 31 4.8 Good, Sl.
Soft 14 600 13.7 300 33 4.8 Fair 600 16.1 450 35 4.8 Fair 16 500 16.8 450 34 4.8 Fair 17 500 21.0 600 32 4.8 Fair 18 500 20.6 300 31 4.8 V. Good 19 600 19.8 300 32 4.8 V. Good 600 18.0 300 32 4.8 V. Good 21 600 17.6 300 33 4.8 V. Good 22 600 17.4 300 32 4.8 V. Good 23 500 7.0 300 7 4.8 V. Good 24 500 14.0 300 14 4.7 V. Good 500 27.0 300 27 7 V. Good 26 600 24.8 300 25 7 V. Good 27 600 24.0 190 24 7 V. Good 28 5D0 6.4 300 34 0 V. Good 29 600 13.5 300 37 4.7 V. Good 600 14.7 450 34 7 V. Good 31 60D 29.0 300 39 7 V. Good 32 600 27.6 300 40 7 V. Good 33 600 26 300 33 0 V. Good Table 5 Run k-Init. k-Aged ~ Closed ~ Density No. Cell Friability 1 .136 - - - 1.62 2 .140 - _ - 1.69 ' 4 - .167 79 29 7 .128 - _ -9 .124 - - -10 .131 - - -12 .134 - - -13 - .141 81 8 13A - .136 81 13 14 .123 - - -15 .121 .145 86 12 16 - .138 85 13 17 - .148 87 35 18 - .155 85 18 19 .123 .146 - -20 - .146 86 20 21 .128 - - -22 .139 - - -23 .132 .139 84 8 28 - .149 90 20 29 - .132 - -33 - .177 81 12 Using apparatus of Figure 1, the process was started by injecting component A into barrel B7 until it was observed exiting the extruder. Component B was then injected to the spacer between barrels B7 and B8, followed by injection of catalyst to barrel 739. Shutdown was performed in reverse order. The machine was purged with methylene chloride.
The product had a compression strength of 26 psi, a density of 2.3 lb./cu. ft. and a K factor (thermal conductivity) of 0.168 BTU/sq.- ft. /°F.
When the machine was taken apart, it was easy to remove the barrels separated by Graphoil paper. The internal surfaces of the barrel in the process section were coated with a thin hard layer of cured material but this was readily removable.
Substantially higher concentration of isocyanate (component A) leads to hard and brittle foam. Substantially higher concentration of polyol (component B) leads to rubbery, soft foam and increased exotherm of reaction.
As the speed of the machine is increased, the cell size of the foam is decreased. Variation of these parameters to provide foam having certain characteristics will be apparent to one skilled in the art.
Example 35 Carbon black dispersion made in the extruder screw Component A: polymeric methyldiisocyanate (MDI) 100.00 parts carbon black 9.29 parts dispersant 1_93 parts surfactant l.7parts Using apparatus of Figure 1, the process was started by inj ecting the ingredients for component A into barrel B7 until it was observed exiting the extruder. The dispersion produced was of better quality than that produced in a Kady mill and registered more than 8 on the Hegman scale.
In a further embodiment of the invention, polyisocyanurate bunstock may be made using an extruder. The bun is cut from an extrudate which is passed from the die of SEP. 18. 2000 2:50PM KIRBY EADES 613 237 0045 ND, 4239 P, 2 the extruder to a conveyor belt having release-coated paper liners on the top, bottom and sides. A kraft paper liner having a polymer coating is suitable for use as a release paper. A 20 ft. conveyor may be used, moving at about 9 to 10 ft./min. The bunstock may be from 4 in. to 2 ft. or more in thickness. The foam is warm as it exits the extruder and is allowed to cure for 4 to 6 days. In a typical example of making bunstock on an extruder, the following formulation was used:
Example 36 Huuatocls made in the Extruder Material nnm Tsocyanare (Miles - Mondur MR) 101 Polymer resin (Iso-ShieldT"' - Plo1) ~8 R-~11 (Atochem - Isotron~" 11 or 141H) 13.81 Catalyst #1 (Air Products - TMR-3) 1.1'7 Catalyst #2a (Air Products - DMEA) .312 Cataxyst #2b (Ashland - DEG) .312 The foam was extruded from a die of an extruder, having a large cross-section, as shown in figures 3 and 4, onto a conveyer lined with paper on the top, bottom and sides, to form bunstock having dimensions of about 27" high x 51~"
wide. The cream time was 28 sec., the gel time was 2 min. 34 sec., the rise time was 3 min. 55 sec. and the tack free time was 4 min. 31. The conveyor speed was about 9 to 10 ft./min.
Bunstock may be extruded at a speed of about 200 lb./min. A
typical bun may be about 2'7" x 51~"x 10 ft. in size and may be cut to smaller blocks, as required. Different levels of carbon black may be used, providing different K-values.
The extruder may alternatively be used to make the filler particle dispersion only, which is then fed to a tank for storage and later use.
When the extruder is used for making both the dispersion and the foam, the cream time and gel time are relatively slow due to the size of the bunstock. The bunstock which is liquid at extrusion onto the conveyor, is firm after reaching the end of the conveyor and being released from the paper liners . The process described allows for large volume bunstock to be made, of very high quality.
Examples 37-48 High Filler Particle Content Foam A number of examples of foams having a high filler particle content were produced using the process explained in conjunction with Figure 2 above.
Table 6 presents the various formulations of materials which were used in the examples and Tables 7a and 7b provide a tabulation of the characteristics of the resultant thermoset foam. The examples illustrate how polymer foams can be made using the extrusion process which can contain in excess of 15 0 filler material.
Test runs were conducted using a ZSK-40 extruder having a 40mm wide extruder. Depending upon the type and size of the ' sheet to be produced, larger capacity extruders are used for commercial production such as extruders having diameters 58mm, 70mm, 92mm, or 120mm. Table 8 provides ranges of preferred processing rates for the various size extruders.

WO 96120966 PCTlUS95100175 Table 6 FORMUhP.TION A B C D E

pbw % pbw % pbw % pbw % pbw %

Polyol Cape 100 24.8100 26 100 22.8100 22.6 100 22.7 Surfact-D.C. 0.8 3 .78 2 .5 2 .5 2 .5 ant 9342 lowing Water 0.5 0.1 0.5 .13 1.40 .3 1.40 .3 1.40 .3 gent Forane 47.5 11.838 9.9 3 9.8 47 10.6 40 9.1 141b HCFC 0 0 0 0 0 0 0 0 6 1.4 CatalystTMR-30 0.84 .2 0.45 .12 0.96 .2 1.25 .3 1.25 .3 OMG 977 2.51 0.6 2.2 .58 .65 .6 3.40 .8 3.40 .8 Polycat 0.54 0.1 0.39 .11 0.57 .1 0.65 .2 0.65 .2 1 0 Filler Alumina 76 19 72.2718.70 0 0 0 77.4017.6 Tri-hydrate Calcium 0 0 0 0 73.8016.80 0 0 0 Carbonate Non- 0 0 0 0 0 0 77.8017.6 0 0 expanded Perlite ISOCYANATE 171.842.7 168.44 14.198.8 208.457.2 208.457.3 ~ Table 7a EXAMPLE

Formulation TypeA A A A B B

Iso Index 2.30 2.50 2.50 2.50 2.50 2.20 2 0 . Average 1.53" 1.56" 1.56" 2.12" 1.28" 1.44"
Thickness Board Density 2.29 2.45 2.54 2.09 2.83 2.48 Core Density 2.10 2.39 2.39 1.86 2.61 2.17 K-Value 0.138 0.136 0.138 O.I35 0.133 0.13 2 5 Compressive 22.41psi19.6psi26.44psi19.34psi32.62psi30.4psi % Closed Cell 82.00% 84.20% 83.30% 83.30% 81.00% 77.30%

Hot Dip good good good good good good Cold Aging 0.00%/ 0.58%/ 0.42%/ 0.00%/ 0.00%/ 0.00%/
(% shrink) 0.42% 0.00% 0.00% 0.00% 0.00% 0.00%
0 machine/crosscut Humid Aging 0.93%/ 0.37%/ 0.37%/ 0.56%/ 0.37%/ 0.37%/
(% growth) 0.45% 0.69% 0.45% 0.00% 0.34% 0.34%
machine/crosscut SUBSTITUTE SHEET (RUIE 26) Table 7b Formulation Type C C D D E E

Iso Index 2.60 2.60 2.50 2.50 2.50 2.50 -Avg. Thickness 1.33 2.50 1.44 2.43 1.44 2.44 Board Density 2.42 2.33 2.38 2.33 2.89 1.99 Core Density 2.28 2.28 2.14 2.14 2.59 1.86 K-Value 0.141 0.141 0.138 0.135 0.138 0.134 Compressive 14.6ps l8.Ops 22.04ps21.82ps22.50p 20.66ps i i i i si i Closed Cell 81.13% 82.17% 83.37% 82.00% 84.19% 82.63%

Hot Dip good good good good good good Cold Aging (% 0.00%/ 0.09%/ 0.17%/ 0.11%/ 0.00%/ 0.08%/
shrink) 0.00% 0.120 0.00% 0.08% 0.00% 0.00%
machine/cross cut Humid Aging (% 0.06%/ 0.12%/ 0.06%/ 0.13%/ 0.00%/ 0.06%/
growth) 0.17% 0.11% 0.12% 0.17% 0.00% 0.17%
machine/cross cut Table 8 Extruder Output Ranaesl Extruder ZSK-40 ZSK-92 C-120 High Range lbs/hr 450 1350 2411 5500 12150 lbs/min 7.5 22.5 40 92 202.5 Low Range lbs/hr 600 1800 3215 7300 16200 lbs/min 10 30 54 ~ 122 270 ft/min - 33-44 58-78 134-177 276-391 -c:alculatea zor 1° tnicx zoam proauct 4y° m ae ana ~.u Ips~cu.
=L. a.n-place density.
while the invention has been described with reference to certain embodiments thereof, it will ba appreciated that variations and modifications may be made without departing , from the spirit and scope of the invention.

Claims (25)

What is claimed is:
1. A method for preparing a thermosetting polymer foam product characterized by:
introducing polyol to a screw of an extruder (4);
introducing isocyanate to the screw of the extruder;
mixing the polyol and the isocyanate in the screw of the extruder;
introducing foaming agent to the screw of the extruder;
introducing catalyst to the extruder at a position proximate to the extruder head of the extruder;
mixing the catalyst with the foaming agent, the isocyanate and the polyol in the extruder to form a composite mixture, thereby reacting the isocyanate and polyol and initiating a foaming reaction in the composite mixture in the extruder in conjunction with extrusion whereby expansion of the composite mixture into a foam takes place outside the extruder.
2. A method according to claim 1 further characterized by introducing filler particles chosen from a group including aluminum trihydrate, perlite, carbon black, diatomaceous earth, polyiso powders, barium sulfate, calcium silicate, and calcium carbonate to the screw of the extruder for inclusion in the composite mixture.
3. A method according to claim 2 further characterized by mixing the filler particles with the isocyanate to prepare a particle/isocyanate mixture before introducing, the particle/isocyanate mixture to the screw of the extruder.
4. A method according to claim 2 further characterized by mixing finely divided carbon black with the isocyanate and filler particles to form a carbon/particle/isocyanate mixture before introducing the carbon/particle/isocyanate mixture so formed to the screw of the extruder.
5. A method according to claim 1 further characterized by mixing surfactant with the polyol to prepare a surfactant/polyol mixture before introducing the surfactant/polyol mixture so formed to the screw of the extruder.
6. A method according to claim 5 further characterized by mixing dispersant with the polyol and surfactant to prepare a dispersant/surfactant/polyol mixture before introducing the dispersant/surfactant/polyol mixture so formed to the screw of the extruder.
7. A method according to claim 2 characterized in that finely divided carbon black is mixed with the filler particles to prepare a filler particle/carbon black mixture before introducing the filler particle/carbon black mixture to the screw of the extruder.
8. A method according to claim 1 characterized in that the foaming agent is chosen from the group consisting of hydrochlorofluorocarbon (HCFC), HC, HFC, CFC and water.
9. A method according to claim 8 characterized in that the foaming agent comprises water and HCFC.
10. A method according to claim 2 characterized in that said filler particles comprise at least 12% by weight of said thermoset polymer foam.
11. A method according to claim 2 characterized in that said filler particles comprise from 15-50% by weight of said thermoset polymer foam.
12. A method according to claim 2 characterized in that said filler particles are introduced at a first position in the extruder, a premix of said polyol and a surfactant is mixed with said filler particles at a second position in the extruder, additional polyol is mixed at a third position in the extruder downstream from said second position, said isocyanate is introduced at a fourth position in the extruder downstream from the third position, said foaming agent is introduced at a fifth position in the extruder downstream from the fourth position, and said catalyst is introduced at a sixth position downstream from said fifth position in the extruder.
13. A method according to claim 2 characterized in that said polyol and filler particles are added at a first position of the extruder, said isocyanate is added at a second position of the extruder, downstream of the first position, said foaming agent is added to the extruder at a third position, downstream of the second position, and said catalyst is added to the mixed polyol, filler particles, isocyanate, and foaming agent at a fourth position of the extruder proximate the extrusion die to forth a catalyzed mixture, and extruding the catalyzed mixture so formed for foaming.
14. A method according to claim 1 characterized by cooling the composite mixture before extruding to maintain temperature below 50°C.
15. A method according to claim 1 characterized in that the extruder is a twin screw extruder and is operated at 300-600 rpm.
16. A method according to claim 1, wherein the catalyst is introduced into a barrel (A12) of the extruder adjacent the extruder head (A46).
17. A method according to claim 1 further characterized by the step of laminating the extruder composite mixture between an upper paper liner and a lower paper liner and thereby forming a laminated insulation sheet.
18. Thermoset polymer product including a foam characterized in that the foam is formed by mixing filler particles, polyol, foaming agent and isocyanate with a catalyst in an extruder and immediately extruding the reactants wherein the filler particles comprise at least 12%
by weight of the thermoset polymer foam.
19. Thermoset polymer foam according to claim 18 wherein the filler particles are chosen from a group consisting of aluminum trihydrate, perlite, carbon black, diatomaceous earth, polyiso powders, barium sulfate, calcium silicate, and calcium carbonate.
20. Thermoset polymer foam according to claim 18 wherein the filler particles comprise between 15%-20% by weight of the thermoset polymer foam.
21. Thermoset polymer foam according to claim 18 wherein the filler particles consist essentially of carbon black and aluminum trihydrate.
22. Thermoset polymer foam according to claim 18 wherein the filler particles comprise at least 15% by weight of the thermoset polymer foam and are chosen from a group consisting of aluminum trihydrate, calcium carbonate and perlite.
23. Thermoset polymer foam according to claim 18 wherein the foam is formed into bunstock.
24. Thermoset polymer foam according to claim 18 wherein the foam is formed into sheets.
25. Thermoset polymer product according to claim 18 further comprising upper and lower paper liners characterized in that said foam is laminated between said upper and said lower paper liners.
CA002209563A 1993-11-01 1995-01-06 Extruded polymer foam and method Expired - Fee Related CA2209563C (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US08/144,621 US5424014A (en) 1992-09-18 1993-11-01 Method for extruding foamable polymer material
PCT/US1995/000175 WO1996020966A1 (en) 1993-11-01 1995-01-06 Extruded polymer foam with filler particles and method

Publications (2)

Publication Number Publication Date
CA2209563A1 CA2209563A1 (en) 1996-07-11
CA2209563C true CA2209563C (en) 2002-06-25

Family

ID=26789444

Family Applications (1)

Application Number Title Priority Date Filing Date
CA002209563A Expired - Fee Related CA2209563C (en) 1993-11-01 1995-01-06 Extruded polymer foam and method

Country Status (10)

Country Link
US (1) US5424014A (en)
EP (1) EP0801660B1 (en)
JP (1) JP3226927B2 (en)
AT (1) ATE206443T1 (en)
AU (1) AU1598995A (en)
CA (1) CA2209563C (en)
DE (1) DE69523070T2 (en)
ES (1) ES2164760T3 (en)
MX (1) MX9704957A (en)
WO (1) WO1996020966A1 (en)

Families Citing this family (38)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
USRE37095E1 (en) * 1992-09-18 2001-03-13 Apache Products Company Extruded polymer foam with filler particles and method
US5723506A (en) * 1992-09-18 1998-03-03 Apache Products Company Extruded polymer foam with filler particles and method
US5846461A (en) * 1996-11-26 1998-12-08 National Foam Cushion Manufacturing, Inc. Method of manufacturing carpet pads from a polyurethane foam composition
US5981611A (en) * 1997-11-24 1999-11-09 Prince Corporation Thermoformable foam with infrared receptors
US6022912A (en) * 1998-09-22 2000-02-08 Bayer Corporation Expansion of polymeric microspheres insitu in a rigid PUR/PIR foam formulation using a twin screw extruder
US6403663B1 (en) 1999-09-20 2002-06-11 North Carolina State University Method of making foamed materials using surfactants and carbon dioxide
ATE362012T1 (en) * 1999-12-20 2007-06-15 Advanced Plastics Technologies HYDROXY-PHENOXYETHER POLYMERS IN PAPER PRODUCTION
AU2001249453A1 (en) * 2000-03-27 2001-10-08 Apache Products Company Fire resistant foam and foam products, method and dispersions for making same
DE10056251B4 (en) * 2000-11-14 2006-06-08 Basf Ag Process for the production of polyurethane foams
WO2002081818A2 (en) 2001-04-04 2002-10-17 Advanced Plastics Technologies, Ltd. Process for coating paper, paperboard, and molded fiber with a water-dispersible polyester polymer
DE10123002C1 (en) * 2001-05-11 2002-08-08 Basf Ag Reaction apparatus for the production of reaction plastics
US7363244B2 (en) * 2002-11-08 2008-04-22 Palo Alto Research Center Incorporated Methods, apparatus, and program products for inferring service usage
US20040102830A1 (en) * 2002-11-22 2004-05-27 Williams Terrell M. System for coupling an implanatable medical device to an epicardial site
US20040219317A1 (en) * 2003-01-22 2004-11-04 Wellstream International Limited Process for manufacturing a flexible tubular pipe having extruded layers made of crosslinked polyethylene
US7763341B2 (en) 2004-01-23 2010-07-27 Century-Board Usa, Llc Filled polymer composite and synthetic building material compositions
US7316559B2 (en) 2004-06-24 2008-01-08 Century-Board Usa, Llc Continuous forming apparatus for three-dimensional foam products
US7794224B2 (en) 2004-09-28 2010-09-14 Woodbridge Corporation Apparatus for the continuous production of plastic composites
US7329374B2 (en) * 2004-12-15 2008-02-12 Lung-Wen Chou Method for manufacturing resing films
JP4694191B2 (en) * 2004-12-17 2011-06-08 住化バイエルウレタン株式会社 Production method of polyurethane foam moldings
WO2007112105A2 (en) * 2006-03-24 2007-10-04 Century-Board Usa, Llc Extrusion of polyurethane composite materials
ES2429171T3 (en) * 2007-12-19 2013-11-13 Sika Technology Ag Monocomponent polymer foam that hardens with moisture
JP5879034B2 (en) * 2007-12-28 2016-03-08 ボスティック,インコーポレイテッド Continuous manufacturing process of moisture curable polyurethane sealants and adhesives
US8846776B2 (en) 2009-08-14 2014-09-30 Boral Ip Holdings Llc Filled polyurethane composites and methods of making same
US9481759B2 (en) 2009-08-14 2016-11-01 Boral Ip Holdings Llc Polyurethanes derived from highly reactive reactants and coal ash
JP2013072038A (en) * 2011-09-28 2013-04-22 Nitto Denko Corp Method for producing thermoplastic resin foam
US9745224B2 (en) 2011-10-07 2017-08-29 Boral Ip Holdings (Australia) Pty Limited Inorganic polymer/organic polymer composites and methods of making same
US9932457B2 (en) 2013-04-12 2018-04-03 Boral Ip Holdings (Australia) Pty Limited Composites formed from an absorptive filler and a polyurethane
TWI667285B (en) 2013-10-18 2019-08-01 德商巴斯夫歐洲公司 Production of expanded thermoplastic elastomer
JP6321404B2 (en) * 2014-02-26 2018-05-09 株式会社ジェイテクト Electric storage material manufacturing apparatus and manufacturing method
US10138341B2 (en) 2014-07-28 2018-11-27 Boral Ip Holdings (Australia) Pty Limited Use of evaporative coolants to manufacture filled polyurethane composites
WO2016022103A1 (en) 2014-08-05 2016-02-11 Amitabha Kumar Filled polymeric composites including short length fibers
WO2016118141A1 (en) 2015-01-22 2016-07-28 Boral Ip Holdings (Australia) Pty Limited Highly filled polyurethane composites
WO2016195717A1 (en) 2015-06-05 2016-12-08 Boral Ip Holdings (Australia) Pty Limited Filled polyurethane composites with lightweight fillers
WO2017082914A1 (en) 2015-11-12 2017-05-18 Boral Ip Holdings (Australia) Pty Limited Filled polyurethane composites with size-graded fillers
KR102154867B1 (en) * 2020-02-07 2020-09-10 최규술 Polyurethane Foam And Manufacturing Method of the Same
EP4001335A1 (en) 2020-11-18 2022-05-25 Covestro Deutschland AG Method for producing polyurethane foams
JP2022159929A (en) * 2021-04-05 2022-10-18 積水化学工業株式会社 Polyol composition, polyurethane resin composition, and polyurethane foam
CN113563555A (en) * 2021-08-17 2021-10-29 长虹美菱股份有限公司 Polyurethane foaming material and foaming process thereof

Family Cites Families (16)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3466705A (en) * 1966-03-07 1969-09-16 Owens Illinois Inc Apparatus for extruding foamable plastic materials in tubular form
DE2649996A1 (en) * 1976-10-30 1978-05-03 Bayer Ag PROCESS AND APPARATUS FOR PRODUCING A FILLER-CONTAINING REACTION MIXTURE FROM AT LEAST TWO FLOWABLE COMPONENTS, IN PARTICULAR FOR PRODUCING POLYURETHANE
DE2707026A1 (en) * 1977-02-18 1978-08-24 Bayer Ag METHOD AND DEVICE FOR CONTINUOUSLY EXTRUDING PLASTIC PROFILES FROM POLYURETHANE RAW MATERIALS
DE2828506C2 (en) * 1978-06-29 1980-04-17 Bayer Ag, 5090 Leverkusen Method and device for producing a foamable mixture of at least two flowable, foam-forming reaction components and additives
DE2854406A1 (en) * 1978-12-16 1980-06-26 Bayer Ag THERMOPLASTIC CHEMICAL MATERIALS AND METHOD FOR THEIR PRODUCTION
DE2854409A1 (en) * 1978-12-16 1980-06-26 Bayer Ag METHOD FOR PRODUCING THERMOPLASTIC CHEMICAL MATERIALS
US4395214A (en) * 1981-08-27 1983-07-26 U.C. Industries Foam extrusion apparatus having downstream upper and lower hinged shaping means and side restraining means
DE3224324A1 (en) * 1982-06-30 1984-01-05 Basf Ag, 6700 Ludwigshafen TWO-STAGE PROCESS FOR PRODUCING THERMOPLASTIC POLYURETHANE ELASTOMERS
DK157908C (en) * 1982-12-22 1990-09-03 John Schmidt BUILDING MATERIAL FOR BUILDING ELEMENTS AND PROCEDURES AND PLANTS FOR PRODUCING IT.
US4496625A (en) * 1983-10-12 1985-01-29 The Celotex Corporation Alkoxylated aromatic amine-aromatic polyester polyol blend and polyisocyanurate foam therefrom
US4795763A (en) * 1988-04-18 1989-01-03 The Celotex Corporation Carbon black-filled foam
US4948859A (en) * 1988-10-28 1990-08-14 Minnesota Mining And Manufacturing Company Extruder polymerization of polyurethanes
US5192607A (en) * 1991-08-28 1993-03-09 The Celotex Corporation Dispersant for carbon black-filled foam
US5149722A (en) * 1991-08-28 1992-09-22 The Celotex Corporation Dispersant for carbon black-filled foam
US5137930A (en) * 1991-08-28 1992-08-11 The Celotex Corporation Dispersant for carbon black-filled foam
US5373026A (en) * 1992-12-15 1994-12-13 The Dow Chemical Company Methods of insulating with plastic structures containing thermal grade carbon black

Also Published As

Publication number Publication date
CA2209563A1 (en) 1996-07-11
ES2164760T3 (en) 2002-03-01
EP0801660A4 (en) 1998-04-08
WO1996020966A1 (en) 1996-07-11
DE69523070T2 (en) 2002-07-04
AU1598995A (en) 1996-07-24
DE69523070D1 (en) 2001-11-08
EP0801660B1 (en) 2001-10-04
ATE206443T1 (en) 2001-10-15
JPH10502415A (en) 1998-03-03
EP0801660A1 (en) 1997-10-22
US5424014A (en) 1995-06-13
MX9704957A (en) 1998-02-28
JP3226927B2 (en) 2001-11-12

Similar Documents

Publication Publication Date Title
CA2209563C (en) Extruded polymer foam and method
US5723506A (en) Extruded polymer foam with filler particles and method
USRE37095E1 (en) Extruded polymer foam with filler particles and method
CA2445076C (en) Low-density cellular wood plastic composite and process for formation
US4795763A (en) Carbon black-filled foam
CA2543712C (en) Apparatus and method for low-density cellular wood plastic composites
Zhang et al. Development of an extrusion system for producing fine‐celled HDPE/wood‐fiber composite foams using CO2 as a blowing agent
AU2002259018A1 (en) Low-density cellular wood plastic composite and process for formation
CA2386282A1 (en) Process and apparatus for making a thermoset foam
KR20160073996A (en) Production of expanded thermoplastic elastomer
CN110283438B (en) Base resin for blow molding degradable film and blow molding degradable film
EP2271695B1 (en) Extruded foams made with polylactides that have high molecular weights and high intrinsic viscosities
US5798064A (en) Process and apparatus for fabrication of flexible foam
CN1054099C (en) Process for the production of products of light cellular plastic with closed cells
EP0376671A2 (en) Method and apparatus for preparing thermoplastic foam
CN103270094A (en) High strength extruded thermoplastic polymer foam
CA1188048A (en) Process for the manufacture of foamed structures
WO1988001934A1 (en) A method for producing cellular pvc plastic
US20070023946A1 (en) Continuous method for producing solid, hollow or open profiles
US20080161437A1 (en) Novel polyisocyanurate foam materials containing CaCO3 filler
RU2167061C2 (en) Method for production of foamed plates with high compressive strength
US20080161434A1 (en) Novel polyisocyanurate foam materials
US9920177B2 (en) Continuous method for producing solid, hollow or open profiles
WO2000017248A1 (en) Process for making rigid polyurethane and polyisocyanurate foams
JP2002530497A (en) Microporous polyvinyl chloride foam

Legal Events

Date Code Title Description
EEER Examination request
MKLA Lapsed