WO2000005296A1 - Particules de polymere thermoplastique expansible et procede de fabrication associe - Google Patents

Particules de polymere thermoplastique expansible et procede de fabrication associe Download PDF

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Publication number
WO2000005296A1
WO2000005296A1 PCT/US1999/001256 US9901256W WO0005296A1 WO 2000005296 A1 WO2000005296 A1 WO 2000005296A1 US 9901256 W US9901256 W US 9901256W WO 0005296 A1 WO0005296 A1 WO 0005296A1
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WO
WIPO (PCT)
Prior art keywords
polymer
particles
process according
blowing agent
thermoplastic
Prior art date
Application number
PCT/US1999/001256
Other languages
English (en)
Inventor
Thomas Orr Craig
George B. Klingensmith
Original Assignee
Huntsman Corporation
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
Priority claimed from PCT/US1998/015446 external-priority patent/WO1999006477A1/fr
Priority claimed from US09/158,189 external-priority patent/US5977195A/en
Application filed by Huntsman Corporation filed Critical Huntsman Corporation
Priority to CA002338464A priority Critical patent/CA2338464A1/fr
Priority to JP2000561250A priority patent/JP2003524667A/ja
Priority to AU22399/99A priority patent/AU2239999A/en
Priority to KR1020017000994A priority patent/KR20010071021A/ko
Priority to BR9912681-8A priority patent/BR9912681A/pt
Priority to EP99902414A priority patent/EP1102808A1/fr
Publication of WO2000005296A1 publication Critical patent/WO2000005296A1/fr
Priority to NO20010367A priority patent/NO20010367L/no

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Classifications

    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
    • C08J9/00—Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof
    • C08J9/16—Making expandable particles
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J2/00—Processes or devices for granulating materials, e.g. fertilisers in general; Rendering particulate materials free flowing in general, e.g. making them hydrophobic
    • B01J2/02—Processes or devices for granulating materials, e.g. fertilisers in general; Rendering particulate materials free flowing in general, e.g. making them hydrophobic by dividing the liquid material into drops, e.g. by spraying, and solidifying the drops
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29B—PREPARATION OR PRETREATMENT OF THE MATERIAL TO BE SHAPED; MAKING GRANULES OR PREFORMS; RECOVERY OF PLASTICS OR OTHER CONSTITUENTS OF WASTE MATERIAL CONTAINING PLASTICS
    • B29B9/00—Making granules
    • B29B9/10—Making granules by moulding the material, i.e. treating it in the molten state
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29C—SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
    • B29C44/00—Shaping by internal pressure generated in the material, e.g. swelling or foaming ; Producing porous or cellular expanded plastics articles
    • B29C44/34—Auxiliary operations
    • B29C44/3461—Making or treating expandable particles
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29B—PREPARATION OR PRETREATMENT OF THE MATERIAL TO BE SHAPED; MAKING GRANULES OR PREFORMS; RECOVERY OF PLASTICS OR OTHER CONSTITUENTS OF WASTE MATERIAL CONTAINING PLASTICS
    • B29B9/00—Making granules
    • B29B9/12—Making granules characterised by structure or composition
    • B29B2009/125—Micropellets, microgranules, microparticles
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
    • C08J2203/00—Foams characterized by the expanding agent
    • C08J2203/06—CO2, N2 or noble gases
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
    • C08J2203/00—Foams characterized by the expanding agent
    • C08J2203/12—Organic compounds only containing carbon, hydrogen and oxygen atoms, e.g. ketone or alcohol
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
    • C08J2203/00—Foams characterized by the expanding agent
    • C08J2203/14—Saturated hydrocarbons, e.g. butane; Unspecified hydrocarbons
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
    • C08J2203/00—Foams characterized by the expanding agent
    • C08J2203/14—Saturated hydrocarbons, e.g. butane; Unspecified hydrocarbons
    • C08J2203/142—Halogenated saturated hydrocarbons, e.g. H3C-CF3
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
    • C08J2203/00—Foams characterized by the expanding agent
    • C08J2203/22—Expandable microspheres, e.g. Expancel®

Definitions

  • This invention concerns a novel method for producing expandable thermoplastic particles. More particularly, the invention relates to expandable polymer particles that may be advantageously produced utilizing an atomization technique. Expansion and fusion of the particles so produced may be conducted using means well-known to those skilled in the art of expandable polymers in order to form various molded products from the particles.
  • the prior art provides methods for manufacturing expandable thermoplastic polymeric materials, including both crystalline and amorphous polymers.
  • Production of expandable thermoplastic materials made from crystalline polymers is effected by heat plastifying a normally-solid polymer resin, admixing such heat plastified resin with a volatile blowing agent under heat and pressure to form a flowable gel, and thereafter extruding the gel into a zone of lower pressure and temperature to expand and cool the gel to form the desired solid polymeric foam product.
  • 1 ,2-dichlorotetrafiuoroethane has been widely used as such a blowing agent owing to the sufficient degree of dimensional stability it confers to masses of foamed products during the curing period.
  • a blowing agent is compounded into the starting polymer resin blend in proportions to make the desired degree of expansion in the resulting foamed cellular product, usually up to about a 60-fold volume expansion to produce products having aged foam densities down to about 9.6 kg/m (about 0.6 pounds per cubic foot).
  • the expandable compositions may be prepared by heat plastifying an olefm polymer resin and mixing the resin with a stability control agent and a blowing agent, and finally activating the blowing agent to expand the mixture.
  • Typical processes for producing such materials are outlined in US Patent numbers 4,694,027; 4,894,395; 5,304,580; and 5,605,937, the entire contents of which are herein incorporated by reference thereto.
  • expandable thermoplastic materials produce particles having less than optimal properties.
  • expandable polyolefm particles such as polyethylene must be pre-expanded prior to impregnation with blowing agent, and such pre-expansion requirement is well-known to those skilled in this art. This necessary pre-expansion equates with a proportional increase the warehousing space required to store the finished expandable particles.
  • shelf life of pre-expanded thermoplastic expandable materials made from normally- crystalline polymers is well-known by those skilled in this art to be far less than desirable.
  • amorphous polymers such as polystyrene materials
  • production of expandable compositions comprising amorphous polymers include a commonly-used batch process wherein raw materials including an aqueous suspension containing styrene monomer, a surfactant, catalyst, and other additives are processed by well-known means under conditions of vigorous agitation to yield spherical polystyrene beads having diameters in the range of about 0.3 to 1.5 millimeters.
  • Such beads are subsequently impregnated with a hydrocarbon or other blowing agent, typically pentane or halogenated hydrocarbons, by charging approximately one hundred parts (by weight) of polymer particles, one hundred parts water, and one part of a concentrated surfactant (or a mixture thereof, such as a mixture of an arylalkyl polyether alcohol and dodecyl benzene sulfonate) into an autoclave along with about three to ten parts of pentane. The mixture is heated to about 170 degrees Fahrenheit under pressure for 3 hours and cooled to room temperature to yield expandable polystyrene beads which are subsequently rinsed, dried, and stored for later use.
  • a hydrocarbon or other blowing agent typically pentane or halogenated hydrocarbons
  • the size of the beads can be controlled by advantageously selecting the processing conditions, including: time, agitation, temperature, pressure, and reactant concentration.
  • this process for producing expandable polystyrene beads is not without several inherent disadvantages, one being that large volumes of water are required to suspend the polystyrene beads during both the polymerization and the impregnation steps. This in reality is a two-fold disadvantage. First ofall, the heat energy input to the water to bring it to the required temperature is forfeit at the end of the impregnation when the water is discharged to the environment. Secondly, prior to such discharge the water must be treated, at additional expense, in order to meet the strict regulatory requirements imposed by various governmental entities. These combined energy and treatment costs are a significant portion of the cost of expandable polystyrene which is passed on to the end- users of the polystyrene.
  • stirred tank reactors in which the suspension is reacted are vulnerable to a multiplicity of events which can cause the reactor agitator to cease in its motion, including power and equipment failures.
  • failures represent potential catastrophic occurrences in that coalescence of monomer droplets may lead to formation of a single, large, reactive mass of material undergoing an uncontrollable, strongly exothermic reaction owing to the lack of effective means for heat removal in such instances.
  • fouling of equipment such a scenario represents a significant safety hazard.
  • Expandable thermoplastic polymeric materials including both those prepared from both crystalline and amorphous materials in accordance with the foregoing containing volatile agents are known to be expandable by application of heat under conditions which permit the volatile agent to be vaporized and form large numbers of cells within the bulk of the polymeric material.
  • heating of expandable thermoplastic materials is performed within the confines of a suitable mold, various articles of manufacture may be produced using the expandable polymeric materials mentioned, regardless of whether the materials exist in the form of pellets or beads.
  • the instant invention also relates to a means for producing expandable polymeric particles of reasonable uniformity in size, to reduce and even preclude the necessity for multi-step particle size classification of the spheroids.
  • the spheroid particles produced in the present invention may contain various additives which include but are not limited to: flame retardants, nucleating agents, and other chemical species which are known to impart desirable properties to polymers. Such other chemical species are well-known to those of ordinary skill in the art.
  • the present invention provides continuous processes for producing expandable thermoplastic spheroidal particles and, which is applicable to both crystalline polymers such as polyolefms and amorphous polymers such as polystyrene.
  • crystalline polymers such as polyolefms
  • amorphous polymers such as polystyrene.
  • expandable polyolefms such materials produced in accordance herewith contain more gaseous blowing agent than those materials made using a prior art method.
  • amorphous polystyrenics the production of such is free from the hazards associated with potential formation of a large mass of exothermally reactive material, as well as the pendant costs for treatment of large volumes of water in pursuance of satisfaction of environmental or other regulatory standards.
  • the processes of this invention comprises providing a molten mixture including a thermoplastic polymer and at least one blowing agent, and fo ⁇ riing particles from the thermoplastic polymer.
  • the particles formed are immediately and rapidly thermally quenched in order to hold in place within the solid matrix the blowing agent which was dispersed throughout the polymer melt.
  • a technique involving atomization of the blowing agent-laden thermoplastic is advantageously conducted to effect a deep thermodynamic quench of the nascent particles in order to lock the blowing agent within the particle matrix.
  • Such formation of particles avoids the difficulties of blowing gas rejection normally associated with polymer crystallization, since the cooling is effected more rapidly than possible using other prior art methods.
  • polymers such as isotactic polypropylene and polyethylene
  • adiabatic cooling which takes place immediately following formation of the particles in an atomization nozzle as elsewhere described herein.
  • an extrusion technique in which the fluid polymer mass is immediately quenched in a liquid cooling bath as it emerges from a die in the form of extrudate may be employed to form particles from thermoplastic polymers in which the liquid cooling bath is selected from cold water, liquid nitrogen, or liquid helium, and the process is similar in fashion as those used to produce lead shot or jeweler's casting granules. This process may be carried out preferably, though not necessarily, in a controlled atmosphere containing the blowing agent under pressure.
  • Pellets may be formed by the action of a cutting surface acting on an extrudate emerging from the die of a conventional polymer extruder, and such pellets fall within the meaning of the word "particles" as used in this specification and the claims appended hereto.
  • rapid cooling of the polymer under conditions which inhibit or delay the rate of crystallization of polymer substantially restricts the ability of a gaseous blowing agent to diffuse out from the bulk of the particles upon cooling.
  • the blowing agent becomes and remains entrapped within the particle. This concept is the common thread shared by the methods herein disclosed.
  • the most preferred method for forming particles is to deliver the molten mixture containing a blowing agent to an atomizing nozzle under conditions sufficient to cause atomization of the molten mixture so as to form droplets comprising the molten mixture, and effecting sufficient simultaneous cooling of the droplets to form polymer particles having the blowing agent entrapped therein.
  • the particles are then collected for later use. This method is applicable to both crystalline and amorphous polymers.
  • expandable polystyrene spheroids may be produced by first providing a stream or a reservoir of a molten polymer mass which contains at least one blowing agent in an evenly distributed form under conditions of temperature and pressure sufficient to ensure that a gas phase does not exist in the molten mass.
  • An atomization nozzle is also provided in fluid contact with the molten mass.
  • the molten material from the polymer stream or reservoir is transferred through an orifice in the nozzle to a region of pressure less than that present in the reservoir or stream.
  • the change in pressure encountered, coupled with the physical configuration of the nozzle and the action of the atomizing gas results in atomization of the molten polymer containing the blowing agent evenly distributed throughout its bulk.
  • the Joule/Thompson cooling attendant to the expansion of the atomizing gas accompanying the atomization, along with any external cooling optionally applied causes the molten polymer to form spheroids containing the blowing agent evenly dispersed therein. Following collection, the spheroids are suitable for use in molding various articles of manufacture using techniques known to those of ordinary skill in the art.
  • the drawing is a cutaway view of an atomizing nozzle useful for producing expandable thermoplastic polymer particles according to the invention.
  • the present invention is a process for producing expandable thermoplastic particles from a polymer melt that contains at least one blowing agent. Particles are produced from this melt using either an extrusion technique in combination with a rapid cooling means, or, as is most preferable, by an atomization process which inherently comprises adiabatic cooling or external cooling.
  • the particles produced are spheroids that may be later used in a molding process well-known to those of ordinary skill in this art.
  • the polymeric spheroid particles comprise polypropylene, polyethylene, or polystyrene.
  • the preferred method for forming expandable thermoplastic particles according to this invention is that wherein a molten stream of polymer containing a blowing agent is fed into an atomizing nozzle under conditions sufficient to cause the rapid formation of particles, and simultaneous or immediate subsequent rapid cooling thereof.
  • particles may be formed from crystalline polymers such as polypropylene and polyethylene, and amorphous polymers such as polystyrene.
  • an extrusion technique is employed to form particles from the mixture, including but not being limited to the direction of a stream of molten thermoplastic material into a quench bath such as cold water, liquid nitrogen, or liquid helium in similar fashion as lead shot or jeweler's casting granules are produced, the whole of the quenching being carried out preferably in a controlled atmosphere containing the blowing agent under pressure.
  • the pressure within the controlled atmosphere is sufficient to substantially reduce any tendency of the blowing agent to become separated from the molten mass.
  • Pellets or barrel shaped chunks of polymer formed by the action of a cutting surface acting on an extrudate emerging from the die of a polymer extruder fall within the meaning of the word "particles" as used in this specification and the claims appended hereto.
  • particle fabrication may be carried out using water as a cooling medium in contact with the extrudate, or using other liquid materials such as liquid nitrogen, liquid helium, or a cold pool of metallic mercury.
  • the crystallinity of freshly-prepared (less than 1 minute old) expandable pellets must be lower than 90 % of the crystallinity of the polymer prior to its being rendered molten and injected or otherwise mixed with blowing agent.
  • This reduced crystallinity is the result of the molten polymer stream having been rapidly cooled according to the teachings herein, and is a direct indication of the effective inhibition or delay of the crystallization of the polymer.
  • the crystallinity of the pellets shall increase to the normally observed value (after correcting for the presence of the blowing agent) for the polymer in question.
  • Blowing agents are generally well-known to those of ordinary skill in the polymer art.
  • a blowing agent employed herein may include any of those well-known in the foamed polymer art as being useful for this purpose including, but not limited to gases including: hydrocarbons, nitrogen, carbon dioxide, halogenated hydrocarbons, fluorinated hydrocarbons, chlorocarbons, chlorofluorocarbons.
  • Solid substances such as azo- dicarbonamide and other well-known compounds which similarly evolve gases suitable for use as blowing agents in polymers when subjected to thermal energy are also herein indicated as being suitable blowing agents for inclusion in the polymer melt.
  • the blowing agent comprises n-pentane, butane, or isobutane.
  • the blowing agent comprises n-pentane.
  • the amount of blowing agent present in the melt is between about 0.5 and 7.0 percent by weight, and when n-pentane is selected as the blowing agent it is present at an amount of between 1.0 % and 10 % and most preferably 5.0 % by weight of the total polymer mass.
  • the molten polymer stream is maintained under conditions of temperature and pressure such that no gaseous pentane is present, and the blowing agent is evenly distributed within the polymer stream melt. Any of various means for agitation, as are well-known to those of ordinary skill, may be employed to promote uniformity of the dispersion of blowing agent in the melt.
  • the atomizing nozzle to which the polymer stream laden with blowing agent is fed may be of various configurations provided that the polymer stream is sufficiently atomized that particles in the size range of about 0.3 to 1.5 millimeters are formed upon the cooling of the atomized polymer.
  • the most preferred nozzles for use in atomizing polymer melts according to this invention are those which employ impingement of a gas stream on a stream or film of molten polymer in order to atomize the stream or film.
  • gas atomization nozzles are disclosed in US Patents 4,619,845 and 5,228,620, the entire contents of which are herein incorporated by reference. Referring to the drawing there is shown a cutaway view of a schematic of an atomizing nozzle useful for preparing particles of expandable polymers according to the present invention. In this figure, 75 represents the polymer particle product.
  • 83 represents a co-extensive construction in which is contained a tubular conduit 71 through which the molten polymer stream 26 is conveyed to atomizing zone 69.
  • 42 is a construction which defines the orifice through which the atomizing gas and molten polymer stream pass.
  • the molten polymer stream is caused to be atomized by virtue of the interaction of the high velocity atomizing gas 17 interacting with the molten polymer stream.
  • the atomizing gas 17 is fed in under high pressure at a sub-sonic rate into the atomizing nozzle where it acts upon the molten polymer stream thus causing the latter to be atomized.
  • the portion 30 from which the atomized particles emerge is a region of lower pressure, preferably atmospheric.
  • Adiabatic cooling or Joule-Thompson cooling is a well-known phenomena to those skilled in the art of physical chemistry, and detailed mathematical and practical descriptions thereof are set forth in the book entitled "Physical Chemistry", written by Peter W. Atkins, 3 ed. and published by W.H. Freeman and Company, New York, 1985 (ISBN-0-7167-
  • Suitable atomization apparatus for the process according to the invention may include, for example, rotary atomization discs or plates, single material and multi- material nozzles with or without auxiliary supply of energy (e.g., mechanical vibration) and mixing nozzles with internal or external mixing.
  • auxiliary supply of energy e.g., mechanical vibration
  • Another nozzle anticipated as being useful herein is the one set forth and described in an article appearing in "Materials World” magazine, Vol. 5, No. 7 (July 1997), pages 383 et seq. (the entire contents of which are herein incorporated by reference).
  • Another requisite for making polymer particles in accordance with this invention is the supplying of a stream of molten polymer liquid into the atomization apparatus described above. This may be accomplished by free inflow from a pressurized container or by means of suitable pumps, extruders, or other melt-conveying devices known in the art.
  • the combination of temperature and pressure required to deliver the polymer melt to the atomizing nozzle at a desired flow rate can be readily calculated from the temperature- viscosity dependence data for the polymer or polymer blend employed.
  • the pressure inside the conduits is greater than atmospheric pressure and is most preferably about 200 psig.
  • the temperature of the polymer melt is at least ten (10) degrees centigrade above the melting point or glass transition point of the polymer.
  • the preferable temperature of the melt is 180 degrees centigrade using 5.0 % pentane in the melt.
  • the liquid stream comprising the polymer melt is supplied to the atomizing nozzle, atomization occurs by virtue of the interaction of the atomizing gas with the polymer melt and the simultaneous change in pressure it experiences.
  • the pressure outside the nozzle is atmospheric pressure; however, pressures other than atmospheric may be used provided that the difference between that experienced by the polymer melt and the external pressure is at least 5 psig..
  • the diameter of the particles produced is preferably between about 0.3 to 1.5 millimeters. The preferred size of the particles varies according to the final application in which their employ is desired, with 1.0 mm diameter being typical.
  • sufficient cooling for rendering the nascent polymer particles exiting the atomization nozzle is employed in order to suppress gas generation from the blowing agent during the stage in which the polymer spheroids are formed, in order that no appreciable net expansion of the particles occurs, and to promote retention of the blowing agent within the solidified particles themselves.
  • a continuous mass polymerization plant producing molten polystyrene at 8000 kg/hr is arranged so that a sidestream of molten polymer can be taken from the plant output stream at a rate of 50 kg/hr using a gear pump.
  • the gear pump delivers the polymer to a static mixer equipped with an injector device through which a volatile substance such as pentane at 5.0% (by weight based on the polymer weight) can be admitted to the molten polymer and dissolved therein.
  • the polymer exiting the static mixer is maintained at a temperature of 210 degrees centigrade by heat transfer oil circulating in a jacket surrounding the static mixer.
  • the polymer passes from the static mixer into the throat of a cooling extruder that cools the molten polymer to 170 degrees centigrade.
  • the polymer exiting the extruder passes to an atomizing diehead comprising a heated vertical pour tube having an internal diameter of 10 mm.
  • the molten polymer emerges as a free-falling strand from the lower end of the pour tube and is impinged upon and atomized by a stream of nitrogen gas.
  • the atomizing stream of nitrogen gas is delivered at a pressure of 17 bar through a plurality of orifices arranged in a circular array having the of the pour tube as the center of the circular array.
  • each orifice impinges on the polymer at an angle of 15 degrees with respect to the axis of the polymer stream which in this case is vertical.
  • a resonant cavity which creates a 50 kHz pressure and velocity oscillation in the nitrogen gas stream.
  • the flow rate of nitrogen is set at 5 cubic meters per hour calculated at standard temperature and pressure.
  • the pentane-laden polymer is atomized by the impinging gas to the form of spheroidal particles having a mean diameter of 1.0 mm.
  • Samples of these particles are heated in boiling water and are thereby expanded to provide low-density foamed polystyrene particles having a closed-cell structure, thus demonstrating that an effective amount of pentane is retained within the nascent polymer particles created by the atomization to cause expansion of the particles.
  • Larger quantities of the particles on the order of 100 kilogram lots are pre- expanded by exposure to steam in a pre-expander of the type conventionally used in the manufacture of expandable polystyrene from suspension-polymerized gas-impregnated polymer beads.
  • the expanded beads are left to mature for 5 hours, and then molded to produce insulation boards having a density of 40 kg/Cu meter and a thermal conductivity of 0.03 watts per meter per degree centigrade.

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  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Engineering & Computer Science (AREA)
  • Mechanical Engineering (AREA)
  • Materials Engineering (AREA)
  • Health & Medical Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Manufacture Of Porous Articles, And Recovery And Treatment Of Waste Products (AREA)
  • Processes Of Treating Macromolecular Substances (AREA)
  • Processing And Handling Of Plastics And Other Materials For Molding In General (AREA)
  • Compositions Of Macromolecular Compounds (AREA)

Abstract

La présente invention concerne un procédé de fabrication de particules de polymère expansible. Ce procédé, continu, permet de produire des granulés de polymère expansible en une seule étape, tout en évitant les dangers inhérents aux précédents procédés de production de ces produits. Les polymères produits à l'aide de cette invention présentent une granulométrie uniforme, et peuvent être moulés afin de produire des articles variés par l'utilisation de dispositifs et de procédés connus.
PCT/US1999/001256 1998-07-24 1999-01-21 Particules de polymere thermoplastique expansible et procede de fabrication associe WO2000005296A1 (fr)

Priority Applications (7)

Application Number Priority Date Filing Date Title
CA002338464A CA2338464A1 (fr) 1998-07-24 1999-01-21 Particules de polymere thermoplastique expansible et procede de fabrication associe
JP2000561250A JP2003524667A (ja) 1998-07-24 1999-01-21 発泡性熱可塑性ポリマー粒子及びその製造方法
AU22399/99A AU2239999A (en) 1998-07-24 1999-01-21 Expandable thermoplastic polymer particles and method for making same
KR1020017000994A KR20010071021A (ko) 1998-07-24 1999-01-21 팽창가능한 열가소성 폴리머 입자 및 그 제조방법
BR9912681-8A BR9912681A (pt) 1998-07-24 1999-01-21 Partìculas expansìveis de polìmero termoplástico e método para sua fabricação
EP99902414A EP1102808A1 (fr) 1998-07-24 1999-01-21 Particules de polymere thermoplastique expansible et procede de fabrication associe
NO20010367A NO20010367L (no) 1998-07-24 2001-01-22 Ekspanderbare termoplastiske polymerpartikler og fremgangsmÕte for fremstilling av slike

Applications Claiming Priority (6)

Application Number Priority Date Filing Date Title
US12251298A 1998-07-24 1998-07-24
PCT/US1998/015446 WO1999006477A1 (fr) 1997-08-01 1998-07-24 Particule thermoplastiques extensibles et procede d'atomisation permettant leur fabrication
USPCT/US98/15446 1998-07-24
US09/122,512 1998-07-24
US09/158,189 1998-09-22
US09/158,189 US5977195A (en) 1997-08-01 1998-09-22 Expandable thermoplastic polymer particles and method for making same

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WO2000005296A1 true WO2000005296A1 (fr) 2000-02-03

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EP (1) EP1102808A1 (fr)
JP (1) JP2003524667A (fr)
CN (1) CN1313876A (fr)
AU (1) AU2239999A (fr)
CA (1) CA2338464A1 (fr)
NO (1) NO20010367L (fr)
WO (1) WO2000005296A1 (fr)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2005056654A1 (fr) * 2003-12-12 2005-06-23 Basf Aktiengesellschaft Granules de polymere de styrene expansible

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* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
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EP0588321A1 (fr) * 1992-09-15 1994-03-23 Montell North America Inc. Procédé pour la fabrication d'objets en mousse de polypropylène
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NO20010367D0 (no) 2001-01-22
CN1313876A (zh) 2001-09-19
CA2338464A1 (fr) 2000-02-03
AU2239999A (en) 2000-02-14
NO20010367L (no) 2001-03-23
JP2003524667A (ja) 2003-08-19

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