WO1991018048A1 - Utilisation d'un agent de nucleation dans un procede de fabrication d'un materiau de garnissage en vrac - Google Patents

Utilisation d'un agent de nucleation dans un procede de fabrication d'un materiau de garnissage en vrac Download PDF

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Publication number
WO1991018048A1
WO1991018048A1 PCT/EP1990/002150 EP9002150W WO9118048A1 WO 1991018048 A1 WO1991018048 A1 WO 1991018048A1 EP 9002150 W EP9002150 W EP 9002150W WO 9118048 A1 WO9118048 A1 WO 9118048A1
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WO
WIPO (PCT)
Prior art keywords
starch
nucleating agent
extruder
granules
material body
Prior art date
Application number
PCT/EP1990/002150
Other languages
German (de)
English (en)
Inventor
Hans Reichenecker
Original Assignee
Storopack Hans Reichenecker Gmbh + 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
Family has litigation
First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=6407028&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=WO1991018048(A1) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by Storopack Hans Reichenecker Gmbh + Co. filed Critical Storopack Hans Reichenecker Gmbh + Co.
Priority to BR9008025A priority Critical patent/BR9008025A/pt
Priority to JP91502046A priority patent/JPH05506675A/ja
Publication of WO1991018048A1 publication Critical patent/WO1991018048A1/fr

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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
    • C08J9/0061—Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof characterized by the use of several polymeric components
    • 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
    • B29C44/02—Shaping by internal pressure generated in the material, e.g. swelling or foaming ; Producing porous or cellular expanded plastics articles for articles of definite length, i.e. discrete articles
    • B29C44/08—Shaping by internal pressure generated in the material, e.g. swelling or foaming ; Producing porous or cellular expanded plastics articles for articles of definite length, i.e. discrete articles using several expanding or moulding steps
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B65—CONVEYING; PACKING; STORING; HANDLING THIN OR FILAMENTARY MATERIAL
    • B65D—CONTAINERS FOR STORAGE OR TRANSPORT OF ARTICLES OR MATERIALS, e.g. BAGS, BARRELS, BOTTLES, BOXES, CANS, CARTONS, CRATES, DRUMS, JARS, TANKS, HOPPERS, FORWARDING CONTAINERS; ACCESSORIES, CLOSURES, OR FITTINGS THEREFOR; PACKAGING ELEMENTS; PACKAGES
    • B65D81/00—Containers, packaging elements, or packages, for contents presenting particular transport or storage problems, or adapted to be used for non-packaging purposes after removal of contents
    • B65D81/02—Containers, packaging elements, or packages, for contents presenting particular transport or storage problems, or adapted to be used for non-packaging purposes after removal of contents specially adapted to protect contents from mechanical damage
    • B65D81/05—Containers, packaging elements, or packages, for contents presenting particular transport or storage problems, or adapted to be used for non-packaging purposes after removal of contents specially adapted to protect contents from mechanical damage maintaining contents at spaced relation from package walls, or from other contents
    • B65D81/09—Containers, packaging elements, or packages, for contents presenting particular transport or storage problems, or adapted to be used for non-packaging purposes after removal of contents specially adapted to protect contents from mechanical damage maintaining contents at spaced relation from package walls, or from other contents using flowable discrete elements of shock-absorbing material, e.g. pellets or popcorn
    • 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
    • C08J9/04—Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof using blowing gases generated by a previously added blowing agent
    • C08J9/06—Working-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 chemical blowing agent
    • C08J9/08—Working-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 chemical blowing agent developing carbon dioxide
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L3/00—Compositions of starch, amylose or amylopectin or of their derivatives or degradation products
    • C08L3/02—Starch; Degradation products thereof, e.g. dextrin
    • 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
    • C08J2201/00—Foams characterised by the foaming process
    • C08J2201/02—Foams characterised by the foaming process characterised by mechanical pre- or post-treatments
    • C08J2201/03—Extrusion of the foamable blend
    • 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
    • C08J2303/00—Characterised by the use of starch, amylose or amylopectin or of their derivatives or degradation products
    • C08J2303/02—Starch; Degradation products thereof, e.g. dextrin
    • 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
    • C08J2425/00—Characterised by the use of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by an aromatic carbocyclic ring; Derivatives of such polymers
    • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02W—CLIMATE CHANGE MITIGATION TECHNOLOGIES RELATED TO WASTEWATER TREATMENT OR WASTE MANAGEMENT
    • Y02W90/00—Enabling technologies or technologies with a potential or indirect contribution to greenhouse gas [GHG] emissions mitigation
    • Y02W90/10—Bio-packaging, e.g. packing containers made from renewable resources or bio-plastics

Definitions

  • the invention relates to the use of a nucleating agent in a method for producing pourable packaging material bodies.
  • Such packaging material bodies are known. These loose-fill, spherical segment-shaped packaging material bodies, which are referred to as "loose-fill", are widely used for packaging transport goods.
  • the known packaging material bodies have the disadvantageous property that they are made of plastic material - such as polystyrene or other polymerization products of the benzene derivative styrene - which can only be disposed of with difficulty after use. This fact is perceived as an eminent disadvantage, especially from the point of view of the constantly increasing environmental and environmental protection awareness.
  • the object of the invention is to provide a method which enables the efficient and economical production of biodegradable "loose-fill" packaging material bodies.
  • the technologies that are suitable for plastic packaging material bodies should be applicable, which is not to be expected, particularly for reasons of simple production.
  • nucleating agent is applied to the surface of granules of starch finely distributed in an amount of 0.1-0.2% based on the weight of the granules and in a grain size of approximately 50 u, that the such granules with nucleating agent are fed to an extruder in which they are converted from their solid to a viscous-liquid state, and that one by the decomposition of the nucleating agent under
  • Starch foam which arises in the extruder, is extruded from the mold opening of an extruder and immediately at the mold opening, before significant expansion has taken place, is cut off, and that the starch particles formed in this way are taken up in a storage container "and after an intermediate storage in a post-expansion unit are expanded to their final dimensions.
  • the measures according to the invention allow, in a particularly advantageous manner, the production of a ' biodegradable' loose-fill 'packaging material body which is distinguished by its high environmental compatibility.
  • the starch used as the base material is a natural product and can be degraded by environmentally occurring microorganisms and / or by its natural aging process without environmentally harmful residues.
  • Figure 1 is a schematic side view of a
  • Figure 2 is a partial side view of the
  • Figure 3 is a broken partial plan view of the
  • Figure 4 is a partially enlarged portion of a
  • FIG. 5 shows a section along the line V-V in FIG. 4,
  • FIG. 6 shows the development of the screw helix of the grooves
  • Figure 7 shows an embodiment of a
  • Figure 8 shows a second embodiment of a
  • Figure 9 shows a third embodiment of a
  • the device required to carry out the method is shown schematically in FIG. 1.
  • Its essential functional complexes consist of a drum 5, an extrusion device 10, a storage container 22, a post-expansion unit 23 and a further storage container
  • the drum 5 has openings 6 and 7 through which starch granules and a nucleating agent (bubble form) are added.
  • the starch granules used here consist of pure starch material. However, it is also possible to use the starch method described Granules which contain admixtures but which do not interfere with the process described below. In the following description the term "starch granules" is used for both types.
  • the nucleating agent was ground extremely finely before being introduced into the drum 5 and has a grain size of approximately 40 ⁇ .
  • the nucleating agent added in an amount of approximately 0.1-0.2 percent by weight is drummed onto the starch granules in the drum 5. This drumming of the nucleating agent onto the starch granules has the effect that they are coated with a layer of the nucleating agent which is firmly adhered by adhesive forces and is uniformly distributed over the surface.
  • the nucleating agent tumbled onto the starch granules serves as an initiator of bubble nucleation in the subsequent extrusion process: this is done by the solid nucleating agent in the extruder 14 decomposing with gas formation.
  • the released gas forms in the viscous-liquid starch mass (see below) a large number of vesicles, which act as "germ cells" of the expanded cell structure Starch material function and thus influence the fine porosity of the resulting starch packaging material body.
  • the amount of nucleating agent introduced into the drum 5 is essentially determined by the decomposition behavior of the nucleating agent under the action of heat taking place in the subsequent extrusion process.
  • the nucleating agent can particularly advantageously consist of a carbonate and an acid component.
  • the acid component then enables, in addition to the decomposition of the carbonate component due to the heat of the extrusion process, a chemical reaction with the carbonate component, which reinforces it
  • the starch granules treated in this way are fed into a filling funnel 17 connected to the extrusion device 10 by means of a conveying device 8 and a conveying line 9.
  • Color pigments or other desired additives may also be added in the filling funnel 17.
  • the extrusion device 10 consists of a drive motor 11, a gear 12, a material feed zone 13 and an extruder 14 and a cutting device 16 which is arranged in front of a mold opening 15 of the extruder 14.
  • the tumbled starch granules reach the material inlet zone 13 via the filling funnel 17 arranged at the end of the conveying line 9.
  • the mixture consisting of the starch granules with the tumbled nucleating agent and any additives added is fed by an extruder screw (not shown in FIG. 1) drawn into the material feed zone 13 of the extruder 14.
  • the starch granules with the Tumbled nucleating agents are carried along by the driving flanks of the extruder screw rotating at a suitably selected speed and are thereby conveyed in the axial direction from the material feed zone 13 of the extruder 14 to the mold opening 15 arranged at the other end of the extruder 14.
  • the continuously increasing core diameter of the extruder screw in the extruder direction causes the starch granules to be subjected to a constantly increasing pressure as they move forward through the extruder 14.
  • the mixture formed from the compacted starch granules and the nucleating agent tumbled thereon is heated to a higher temperature until it melts and thereby changes into a viscous-liquid state.
  • the nucleating agent is evenly and finely distributed in the viscous-liquid starch-nucleating agent mixture. This is necessary in order to obtain a regular and fine cell structure of the expanded starch material after extrusion.
  • the drumming of the nucleating agent onto the starch granules has the effect that when the individual granules are rubbed against one another, there is only extremely little abrasion of the nucleating agent due to the pushing or rotating movement of the extruder screw. This prevents the nucleating agent from passing through the starch granules Material feed zone 13, in which no phase transition takes place yet, accumulates in the spaces between the individual granules.
  • the squeezing and shearing of the starch granules caused by the rotary movement of the extruder screw also improves the mixing of starch and nucleating agent without the "short-range order" caused by the tumbling of the nucleating agent being destroyed in the microscopic range of the starch-nucleating agent mixture.
  • This has the advantage that even after the starch granules have passed from their solid phase to their viscous-liquid phase, there is still a very fine and very regular spatial distribution of the solid nucleating agent. However, this means that a volume element contains a large number of finely divided nucleating agent granules which act as bubble nucleating agents.
  • the finely divided nucleating agent decomposes due to the heat with the formation of gas.
  • the heat input caused by the temperature prevailing in the extruder of approx. 110 ° -130 ⁇ C results, in conjunction with the frictional heat generated by the friction of the starch granules, in a thermal splitting of the carbonate component of the nucleating agent, as a result of which carbon dioxide gas is released.
  • This gas release of the nucleating agent leads to the above-mentioned formation of bubble nuclei in the viscous liquid starch material. Because of the fine and almost homogeneous Distribution of the nucleating agent is achieved - seen over the entire volume - even distribution of bubble germs. This extensive homogeneity in the spatial distribution of the bubble nuclei caused by the decomposing nucleating agent represents an essential basis for the fine porosity of the packaging material bodies to be produced.
  • a so-called direct gassing with a suitably selected blowing agent gas is carried out while the starch mixture is being heated. This causes the blowing agent to get into the viscous liquid starch mass and to be dissolved therein. This is due to the pressure and temperature conditions prevailing in the extruder 14
  • Starch-nucleating agent mixture supersaturated with propellant gas, i.e. more propellant gas dissolves than under normal conditions.
  • propellant gas i.e. more propellant gas dissolves than under normal conditions.
  • starch granules in which the propellant gas is contained right from the start.
  • the dissolved propellant gas now diffuses into the bubble nuclei caused by the decomposition of the nucleating agent and causes them to expand.
  • the growth of the bubbles is essentially dependent on the
  • Starch-nucleating agent mixture and the pressure difference between the pressure prevailing in the extruder and the Partial pressure of the blowing agent dissolved in the viscous-liquid starch-nucleating agent mixture is determined.
  • the starch-nucleation mixture emerges from the mold opening 15 of the extruder 14 in the form of a mass of melted starch foam.
  • the starch strand emerging from the mold opening 15 is cut off by the cutting device 16 immediately after it emerges.
  • the cut-off starch particles then expand in free fall into a first expanded state, where they already assume their shape. This expansion is accompanied by simultaneous cooling, so that the bodies solidify shortly behind the mold opening 15 or the cutting device 16 - and before they have reached the collecting container 19.
  • the cooled and solidified starch particles 18, which are in their first expanded state, are collected in the collecting container 19 and conveyed by a blower 20 through a collecting line 21 to the storage container 22.
  • the starch particles 18 produced in this way can be used for various purposes - such as Packing material.
  • the starch particles 18 can be conveyed out of the storage container 23 into a post-expansion unit 23.
  • the starch particles 18 expand again after exposure to heat, so that "loose-fill” packaging material bodies of lower mass density are formed, which advantageously have a substantially lower bulk density. It is essential in this post-expansion step that the heat required for renewed expansion is introduced “dry”. It is therefore not allowed to use hot steam to introduce heat. A "wet" treatment would lead to the destruction of the starch packaging material bodies.
  • the re-expanded starch particles 18 are fed to a further storage container 24.
  • This preferably consists of screen fabric or another open-mesh material, so that free air circulation and thus easy drying of the re-expanded starch particles 18 is made possible.
  • starch granules are fed to a specially designed material feed zone 13 of the extruder 14.
  • This "slot entry zone" shown in detail in FIGS. 2-6 has the effect that the material throughput can be approximately doubled with the same speed of rotation of the extruder screw. This increased throughput of starch material brings about an increased production rate of the process in a particularly advantageous manner.
  • the material feed zone 13 is connected on the right-hand side to a reduction gear 25 which is driven by a motor 11.
  • the melting zone 26 adjoins the material feed zone 13, in which the starch material changes from its solid to the viscous-liquid state. It is essential here that the melting zone 26 and the material feed zone 13 are thermally insulated along their connection 27.
  • the extruder screw extends through the material feed zone 13 and the melting zone 26 and is driven by the motor 11 via the reduction gear 25.
  • the extruder screw is guided in the material feed zone 13 in a bushing 28 which is held by a carrier 29.
  • the bushing 28 is provided with an opening 30 through which the starch material is drawn from the hopper 17 into the extruder 14.
  • the underside 31 of the filling funnel 17 is connected to a flange 32 of the carrier 29.
  • the area of the bushing delimited by the opening 30 forms the groove entry zone 33.
  • the area of the bushing 28 adjoining this groove entry zone 33 in the conveying direction of the extruder screw comprises a transition zone 34.
  • the grooves 35 In the area of the groove entrance zone 33, the grooves 35 have a constant incision depth 36.
  • the incision depth 36 decreases to zero in the conveying direction.
  • the opening 30 in the socket 28 has a length of approximately 80 mm and a width of 50 mm.
  • the transition zone 34 has a length of approximately 185 mm.
  • the socket 28 has a wall thickness 37 of approximately 13 mm.
  • FIG. 4 shows an enlarged section of a bushing 28 in the area of the groove entry zone 33 with grooves 35 which have a constant depth of cut 36.
  • the grooves 35 have a cross-sectionally U-shaped profile 38, the two legs 39 of which are inclined outward by an angle Ct.
  • the angle of inclination 0 is 15 ° in the present exemplary embodiment.
  • the depth of cut 36 of the grooves 35 is approximately 1.5 mm.
  • the width 40 of the grooves 35 is approximately 10 mm.
  • the grooves in the exemplary embodiment described here have a constant distance 41 from one another which is approximately 15.5 mm.
  • the distance between the grooves is determined by the diameter of the bushing 28 and the number of incised grooves 35 and their width is determined.
  • FIG. 5 shows a section along the line V-V in FIG. 4, which runs through a groove 35.
  • the grooves 35 viewed in the direction of transport of the extruder screw, have an initial region 42 at the start of the bush 28, after which they reach their maximum incision depth 36, which is then constant in the groove input zone 33.
  • FIG. 6 shows the development of the groove helix in the material feed zone 13.
  • the bushing 28 is cut open in the longitudinal direction and has a rectangular contour in the rolled-out state.
  • Eight grooves 35 are cut at regular intervals around a circumference 43 of the socket 28.
  • the helix helix has made a full 360 "turn in the transport direction after a section 44.
  • the section 44 is approximately 203 mm.
  • “Loose-fill" packaging material body using the device just described is carried out as follows: The starch material is drawn through the opening 30 into the socket 28. The extruder screw pulls the starch granules into the space between the extruder screw and the groove entry zone 33, which is provided with grooves 35 with a constant depth of cut 36. The starch granules, which have an average core diameter of 0.5 mm, for example, can escape into the grooves 35 in the groove entrance zone 33. As a result of this mobility and the possibility of evasion, fewer starch granules simultaneously rotate in a circle with the extruder screw, so that more starch material can be brought into the transition zone 34 through the extruder screw in the direction of transport.
  • the starch granules are packed and consolidated more tightly.
  • cooling fins 45 are arranged around the bushing 28 in the transition zone 34 in order to allow heat to be dissipated.
  • the transition zone 34 is thermally insulated from the melting zone 26.
  • the core size of the starch granules to be processed can be varied within a certain range without significantly reducing the advantageous effect of the method and the device described.
  • the bushing 28 in the groove input zone 33 can also be provided with cooling fins, so that it is always ensured that the starch material does not change into the viscous-liquid state in the entire material feed zone 13. Such a phase transition of the solid starch granules would "smear" the grooves 35 and would not allow their advantageous effect to come into play.
  • Figure 7 shows a preferred form of a
  • Starch packing material body 50 It has the shape of a 25-28 mm long block or rod with the cross-section of two hollow tubes 51, 52 connected via a short web 53. The shape arises with a corresponding design of the mold opening 15. As indicated, the The surface of the starch packaging material body 50 still exhibits a certain irregularity due to the homogenization of the starch extrusion process by using the nucleating agent, but this leads to an increased friction of such Packing material body leads to each other and can therefore be quite advantageous.

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  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Mechanical Engineering (AREA)
  • General Chemical & Material Sciences (AREA)
  • Manufacture Of Porous Articles, And Recovery And Treatment Of Waste Products (AREA)
  • Extrusion Moulding Of Plastics Or The Like (AREA)
  • Compositions Of Macromolecular Compounds (AREA)
  • Polysaccharides And Polysaccharide Derivatives (AREA)

Abstract

On décrit l'utilisation d'un agent de nucléation dans un procédé de fabrication d'un matériau de garnissage en vrac constitué par de l'amidon. L'agent de nucléation est finement réparti à la surface de grenailles d'amidon, en une quantité de 0,1 à 0,2 % du poids de grenailles et appliqué à une granulométrie d'environ 40 νm. Les grenailles ainsi enduites de l'agent de nucléation sont envoyées dans une extrudeuse (14) dans laquelle elles passent de leur état solide à l'état de fluide visqueux, de façon qu'une mousse d'amidon formée par décomposition de l'agent de nucléation par la chaleur dans l'extrudeuse (14) soit extrudée à l'ouverture de la filière (15) de ladite extrudeuse (14), et soit découpée immédiatement au niveau de cette ouverture (15), avant qu'une expansion importante se produise. Les particules d'amidon ainsi formées (18) sont recueillies dans un récipient de stockage (22), puis sont expansées à leurs dimensions définitives après stockage intermédiaire dans une unité d'expansion subséquente (23).
PCT/EP1990/002150 1990-05-23 1990-12-11 Utilisation d'un agent de nucleation dans un procede de fabrication d'un materiau de garnissage en vrac WO1991018048A1 (fr)

Priority Applications (2)

Application Number Priority Date Filing Date Title
BR9008025A BR9008025A (pt) 1990-05-23 1990-12-11 Emprego de um agente de nucleacao em um processo para a producao de corpos de material de embalagem descarregaveis a granel
JP91502046A JPH05506675A (ja) 1990-05-23 1990-12-11 ばらの詰物を製造するための方法における核形成剤の用途

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
DE19904016597 DE4016597A1 (de) 1990-05-23 1990-05-23 Verfahren zur herstellung schuettfaehiger, kugelsegmentfoermiger packmaterialkoerper mit aussen konvexer und innen konkaver oberflaeche
DEP4016597.3 1990-05-23

Publications (1)

Publication Number Publication Date
WO1991018048A1 true WO1991018048A1 (fr) 1991-11-28

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ID=6407028

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/EP1990/002150 WO1991018048A1 (fr) 1990-05-23 1990-12-11 Utilisation d'un agent de nucleation dans un procede de fabrication d'un materiau de garnissage en vrac

Country Status (6)

Country Link
EP (1) EP0530194A1 (fr)
JP (1) JPH05506675A (fr)
AU (1) AU645285B2 (fr)
BR (1) BR9008025A (fr)
DE (3) DE4016597A1 (fr)
WO (1) WO1991018048A1 (fr)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE4317694A1 (de) * 1993-05-27 1994-12-01 Biotec Biolog Naturverpack Formteil aus Stärkeschaumstoff
EP0712883A1 (fr) * 1994-11-10 1996-05-22 National Starch and Chemical Investment Holding Corporation Produits formés à base d'amidon expansé et méthode pour leur préparation

Families Citing this family (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE4317693C2 (de) * 1993-05-27 1998-07-16 Biotec Biolog Naturverpack Variables Formteil insbesondere aus nachwachsenden Rohstoffen
DE4333909A1 (de) * 1993-10-05 1995-04-06 Helmut Nonnenmacher Verfahren zum Herstellen von Hüll- oder Füllstoffen
DE10052543A1 (de) * 2000-10-23 2002-04-25 Artur Fischer Tip Gmbh & Co Kg Formgebungswerkzeug zum Rundformen eines aus einem festen Schaum bestehenden, plastisch verformbaren Spielbausteins und Verfahren zur Herstellung eines Hohlkörpers aus einem aus einem festen Schaum bestehenden Spielbaustein
DE20019715U1 (de) 2000-11-20 2001-02-22 Artur Fischer Tip Gmbh & Co Kg Formgebungswerkzeug zum Rundformen eines aus einem festen Schaum bestehenden, plastisch verformbaren Spielbausteins
DE10154469A1 (de) 2001-11-08 2003-05-22 Artur Fischer Tip Gmbh & Co Kg Verfahren zur Herstellung einer Spiel- und Konstruktionsbauplatte
DE10321616A1 (de) * 2003-05-13 2004-12-02 Artur Fischer Tip Gmbh & Co. Kg Verfahren zur Herstellung von Malfarbe
DE102004048748A1 (de) * 2004-10-05 2006-04-06 Artur Fischer Tip Gmbh & Co. Kg Palette für Farben

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DE2309577A1 (de) * 1973-02-26 1974-09-05 Urban Manurba Plastik Verfahren und vorrichtung zur herstellung von ersatzholzwolle aus kunststoff
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EP0712883A1 (fr) * 1994-11-10 1996-05-22 National Starch and Chemical Investment Holding Corporation Produits formés à base d'amidon expansé et méthode pour leur préparation

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JPH05506675A (ja) 1993-09-30
DE4016597A1 (de) 1991-11-28
BR9008025A (pt) 1993-05-18
DE9017926U1 (de) 1993-02-25
AU645285B2 (en) 1994-01-13
DE4016597C2 (fr) 1992-04-16
AU7050691A (en) 1991-12-10
EP0530194A1 (fr) 1993-03-10
DE9017904U1 (de) 1993-01-21

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