EP0131015A1 - Anordnung, kunststoffingredienten und eine verstärkung enthaltend - Google Patents

Anordnung, kunststoffingredienten und eine verstärkung enthaltend

Info

Publication number
EP0131015A1
EP0131015A1 EP84900317A EP84900317A EP0131015A1 EP 0131015 A1 EP0131015 A1 EP 0131015A1 EP 84900317 A EP84900317 A EP 84900317A EP 84900317 A EP84900317 A EP 84900317A EP 0131015 A1 EP0131015 A1 EP 0131015A1
Authority
EP
European Patent Office
Prior art keywords
arrangement
ingredients
reinforcement
accordance
plastic
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.)
Withdrawn
Application number
EP84900317A
Other languages
English (en)
French (fr)
Inventor
Jan Christensen
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.)
Rovac AB
Original Assignee
Rovac AB
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 Rovac AB filed Critical Rovac AB
Publication of EP0131015A1 publication Critical patent/EP0131015A1/de
Withdrawn legal-status Critical Current

Links

Classifications

    • BPERFORMING OPERATIONS; TRANSPORTING
    • B29WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29CSHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
    • B29C44/00Shaping by internal pressure generated in the material, e.g. swelling or foaming ; Producing porous or cellular expanded plastics articles
    • B29C44/02Shaping 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
    • B29C44/04Shaping 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 consisting of at least two parts of chemically or physically different materials, e.g. having different densities
    • B29C44/06Making multilayered articles
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B29WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29CSHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
    • B29C37/00Component parts, details, accessories or auxiliary operations, not covered by group B29C33/00 or B29C35/00
    • B29C37/006Degassing moulding material or draining off gas during moulding
    • B29C37/0064Degassing moulding material or draining off gas during moulding of reinforced 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
    • B29C44/02Shaping 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
    • B29C44/12Incorporating or moulding on preformed parts, e.g. inserts or reinforcements
    • 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
    • B29C44/20Shaping by internal pressure generated in the material, e.g. swelling or foaming ; Producing porous or cellular expanded plastics articles for articles of indefinite length
    • B29C44/32Incorporating or moulding on preformed parts, e.g. linings, inserts or reinforcements
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B29WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29CSHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
    • B29C70/00Shaping composites, i.e. plastics material comprising reinforcements, fillers or preformed parts, e.g. inserts
    • B29C70/04Shaping composites, i.e. plastics material comprising reinforcements, fillers or preformed parts, e.g. inserts comprising reinforcements only, e.g. self-reinforcing plastics
    • B29C70/06Fibrous reinforcements only
    • B29C70/10Fibrous reinforcements only characterised by the structure of fibrous reinforcements, e.g. hollow fibres
    • B29C70/12Fibrous reinforcements only characterised by the structure of fibrous reinforcements, e.g. hollow fibres using fibres of short length, e.g. in the form of a mat
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B29WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29CSHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
    • B29C70/00Shaping composites, i.e. plastics material comprising reinforcements, fillers or preformed parts, e.g. inserts
    • B29C70/04Shaping composites, i.e. plastics material comprising reinforcements, fillers or preformed parts, e.g. inserts comprising reinforcements only, e.g. self-reinforcing plastics
    • B29C70/28Shaping operations therefor
    • B29C70/40Shaping or impregnating by compression not applied
    • B29C70/50Shaping or impregnating by compression not applied for producing articles of indefinite length, e.g. prepregs, sheet moulding compounds [SMC] or cross moulding compounds [XMC]
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B29WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29CSHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
    • B29C70/00Shaping composites, i.e. plastics material comprising reinforcements, fillers or preformed parts, e.g. inserts
    • B29C70/04Shaping composites, i.e. plastics material comprising reinforcements, fillers or preformed parts, e.g. inserts comprising reinforcements only, e.g. self-reinforcing plastics
    • B29C70/28Shaping operations therefor
    • B29C70/54Component parts, details or accessories; Auxiliary operations, e.g. feeding or storage of prepregs or SMC after impregnation or during ageing
    • B29C70/542Placing or positioning the reinforcement in a covering or packaging element before or during moulding, e.g. drawing in a sleeve

Definitions

  • the present invention relates to an arrangement comprising plastic ingredients and reinforcement enclosed inside a tightly sealed plastic film cover in which the ingredients are intended to assume a de-activated condition, in which a chemical process for the transformation of the ingredients into a finished plastic material is not initiated, and an activated condition, in which the process is initiated.
  • the principal object of the present invention is to propose an arrangement which, amongst other things, will solve the problem outlined in the foregoing.
  • the plastic ingredients consist of a base material contained inside the plastic film cover in a moisture-proof fashion together with the appropriate initiator and activator for polymerization to nylon-6 or nylon-6 copolymers, whereby polymerization is capable of being initiated only at a temperature, for instance of about 150oC, which is considerably higher than the temperature or the temperatures achieved during the manufacture and storage of the arrangement.
  • the reinforcement preferably being glass fibre reinforcement
  • the reinforcement should then preferably account for about 30 per cent by weight of the total weight of the arrangement.
  • the arrangement should preferably also be of relatively thin execution, for example 1-3 mm in thickness.
  • the plastic film cover is made of nylon.
  • the cover is made of polyolefine, polyester or fluorinated vinyl polymer.
  • the plastic film is comparatively thin, preferably between 0.02 and 0.2 mm in thickness.
  • the base material is also metered in order to compensate for shrinkage due to polymerization.
  • the composition of the ingredients of the unit, the geometrical position of the ingredients inside the unit and the external form of the unit must be determined with great accuracy in the course of the manufacture of the unit, which may be achieved by the use of a computer-controlled production process.
  • the plastic cover may be part of or may be separated from the unit when it is activated or transformed into a finished product.
  • the unit may be executed with internal walls or with internal pockets and/or may be provided with an inner unit which, for the purpose of separation, encloses those ingredients which are to form part of said chemical process when the unit is activated.
  • the base material is liquid at temperatures in excess of 69oC, and polymerization will only occur at a temperature of about 140oC.
  • the base material may be brought during manufacture to a temperature, for instance of about 70-75oC, which is not critical from the point of view of polymerization.
  • a glass fibre mat for example, may be dipped into or sprayed with the base material containing an initiator and an activator.
  • ambient temperature (20-25°C) the material will have solidified, and an essentially dry and rigid filling can then be enclosed by the thin plastic film cover. Transport and storage are simplified in this way.
  • the proposed arrangement also enables a finished product to be produced in nylon-6 or nylon-6 copolymers with long fibres (glass fibre) or continuous and possibly braided fibre mats (in glass). Until now it has been possible to execute the reinforcement in nylon-6 products only in the form of millimetre-thick glass fibres.
  • Moisture-proof enclosure can be provided with the help of a vacuum chamber inside which the humidity level is kept down by the use of low pressure, for example 0.1-0.3 bar. Enclosure can also make use of an inert gas (nitrogen gas), if necessary in combination with the use of a vacuum chamber.
  • an inert gas nitrogen gas
  • the finished product is then conditioned in order to produce increased tenacity (toughness) in the material.
  • a very advantageous external structure can be achieved which does not require any further processing, for example in the form of grinding, washing and/or cleaning, but which may be painted or finished in some other way directly.
  • the characteristics built into the unit in the course of its manufacture mean that it can be stored for lengthy periods (in some cases for a number of months).
  • Figure 1 shows a perspective view seen from above and from the right of a first arrangement or a semi-manufactured item, and of an identical arrangement joined to said first arrangement and illustrated in part only;
  • Figures 2a-2b show respectively a horizontal and a side view of a second arrangement
  • Figure 3 shows in vertical longitudinal section a low-pressure chamber inside which the production of a semi-manufactured item can take place
  • Figures 4a-4b show in diagrammatic form the underlying principle of a production line for a third arrangement.
  • Figure 1 shows two arrangements or units 1 and 2 applied to a base U , said arrangements or units being joined together by means of a connecting piece 3 and 4 along one edge of each unit.
  • the units may also be separate or connected to other units.
  • Each unit is represented as a polygon, in particular as a square or rectangular unit having a length L , a width 8 and a thickness H .
  • the thickness is selected so as to permit thin finished products to be produced having a thickness preferably of between 0.5 and 5.0 mm, and in particular of between 1 and 3 mm.
  • the unit may, however, be tailor-made (pre-moulded) for each particular application and may accordingly exhibit other shapes depending on the intended application.
  • Each unit comprises a thin (e.g. 0.02 - 0.2 mm) cover of plastic material, referred to here as a plastic film cover 5 , and ingredients 6 contained inside the plastic cover and so arranged that, with the unit in its storage or transport position, they do not take part in a mutual chemical reaction for the purpose of producing a finished plastic material, and that, with the unit in an activation and utilization position initiated by means of an activation process, they take part in said chemical reaction.
  • a thin (e.g. 0.02 - 0.2 mm) cover of plastic material referred to here as a plastic film cover 5
  • ingredients 6 contained inside the plastic cover and so arranged that, with the unit in its storage or transport position, they do not take part in a mutual chemical reaction for the purpose of producing a finished plastic material, and that, with the unit in an activation and utilization position initiated by means of an activation process, they take part in said chemical reaction.
  • each unit When viewed from the outside, each unit may be executed in a more or less rigid form depending, amongst other things, on the viscosity of the enclosed ingredients and on any reinforcement.
  • the plastic cover 5 encloses the ingredients 6 in an essentially air-tight condition and, in the embodiment shown here, in an air-evacuated condition.
  • the type of the plastic cover may vary depending on whether the cover is to be included as part of the finished plastics material or is to be used as a means of protection in, amongst other things, moulds which will possibly be used for the final moulding of and/or for combination with some other part of the unit.
  • the cover which, as a general rule, will be wished to be flexible, may be selected from amongst the following groups of materials, for example: the polyolefins, the polyamides, the polyesters or the fluorinated vinyl polymers.
  • the plastic cover is welded or is joined in some other fashion (e.g. by glueing) around its outside edges, of which 3, 3a and 3b are shown here.
  • the plastic film must be capable of being glued or welded and must as a rule be capable of being stretched and must exhibit low permeability by liquid ingredients.
  • the plastic cover may in a typical embodiment be executed with barrier walls and pockets for the purpose of forming various spaces inside the unit. This will enable different ingredients to be kept separate inside the various spaces.
  • a barrier wall of this kind is indicated as a broken line by the reference designation 7 .
  • the plastic cover itself may also be double, whereby the first (outer) plastic cover is given a first characteristic and the second (inner) plastic cover is given a second characteristic.
  • Each unit is a geometrical fit with, or can be made to fit the shape of the object or the addition to said object which the unit is to form.
  • Figures 2a and 2b illustrate typical examples of the unit E which has been pre-moulded during manufacture so as to provide a good fit with the final shape of, for example, a chair.
  • the edge E' may be welded or glued together in a previously disclosed manner using previously disclosed welding or glueing organs S .
  • the quantity of material which the unit represents or includes is in itself sufficient to form the object or the addition. It will be necessary to waste only a small amount of material.
  • the distribution of the ingredients inside the unit is provided (controlled) preferably at an optimum level in the course of manufacture, which is also true of the composition of the ingredients.
  • Figure 3 illustrates a more detailed example of the construction and manufacture of the unit.
  • the unit should be produced in an essentially moisture-free environment preferably inside a chamber 8 at a pressure well below atmospheric pressure, e.g. about 10-30 kpa (0.1 - 0.3 bar) or below. The entrapment of moisture and air is eliminated to a very great extent in this way.
  • the unit in accordance with the invention will form a reinforced (glass fibre-reinforced) semi-manufactured product in nylon-6 or in a nylon-6 copolymer
  • a film 9 of nylon-6 or a similar material are laid one or more thin glass fibre mats prepared beforehand in an appropriate manner.
  • Said mat or mats are impregnated with monomer/monomers, an initiator and an activator for the polymerization reaction.
  • the materials are heated to bring them to a suitable viscosity, for example to a temperature of 70-75oC. Impregnation may then take place by spraying, for example by means of the sprayer organ 12 , or by dipping.
  • the glass fibre mat Once the glass fibre mat has been coated with the aforementioned ingredients it is cooled, causing the coated material to solidify, thereby producing a relatively dry and rigid, impregnated glass fibre mat. It is, of course, possible to build up in accordance with the above several layers of the impregnated glass fibre mat. Similarly, the impregnation of the fibre-glass fabric or the glass fibre mat may take place before the preparation operation.
  • a film 13 of nylon-6 (in accordance with the above) is laid on top.
  • Said upper and lower sheets 9, 13 are then joined together, either by welding or by glueing, so as to form a tightly sealed cover.
  • the welding organs and/or the glueing organs 14a, 14b and 15a, 15b may be executed from previously disclosed elements and are so arranged as to be capable of being moved around the peripheral edge of each semi-manufactured item.
  • the organs 14a, 14b and 15a, 15b are also capable of being moved in other directions towards and away from each other.
  • a base for the film 9 is indicated by the reference designation 16 and clamping organs for the films are indicated by the reference designations 17a, 17b and 18a, 18b .
  • the film 13 is capable of being unrolled over the finished laminate by means of an organ 19 , for example an unrolling organ capable of being moved over the laminate.
  • the flow of material leaving the application organ 12 is indicated by the reference designation 20 .
  • the end 13 of the film is shown by means of a broken line.
  • the chamber is provided with air evacuation equipment 21 and 22 which also incorporates air de-humidification organs 21a, 22a and temperature-controlling equipment 21b and 22b of a previously disclosed kind.
  • the parts of the equipment 21 and 22 are joined together via a line 23 which extends through the wall of the chamber 8 .
  • Material containers 24 for the base material and for the initiator and the activator are connected via the line 25 .
  • the organ 12 can be controlled by a robot 26 in a previously disclosed fashion in various directions 27a, 27b .
  • Fibre mats 10, 11 and film 9, 13 can be introduced via a door 8a in the chamber.
  • the finished material can be made to contain only very small quantities of entrapped gas, for example not more than of the order of 0.5 per cent by volume, and for example 0.2-0.3 per cent by volume of the total volume of the unit.
  • the chamber is able, as an alternative to the moisture-free enclosure environment, to form by means of negative pressure and the air evacuation organ an enclosure environment containing an inert gas, for example nitrogen gas, which eliminates the problems associated with entrapped moisture.
  • the equipment 21,22 may, either as an alternative or in addition, incorporate organs 21c, 22c to guarantee the supply of the nitrogen environment into the chamber.
  • the initial temperature at which said polymerization will usually begin is about 130-150°C.
  • the expression monomer used in connection with nylon-6 shall be understood to denote ⁇ -caprolactam in this context.
  • the expression initiator denotes a compound from one of the following groups: the alkali metals; the alkali earth metals; the oxides, hydrides or alcolates of the last-mentioned metals; or their compounds with the lactams, in this case sodium caprolactamate.
  • the expression activator is used in this context to dunote an acylating compound, in this case a prepolymer isocyanate.
  • nylon-6 copolymers When using nylon-6 copolymers, use may be made of the complete systems which are generally available on the market, for example a system marketed by Monsanto under the name Nyrim 2025 MG.
  • the unit may, in accordance with Figures 4a-4d, also be used in the production of a semi-manufactured item, for example for a door with windows.
  • a sheet 28 of nylon-6 (Capran ER 20) is vacuum-formed to the appropriate initial dimensions of a semi-manufactured blank for a door 29 , the outline for the window of which is indicated by the reference designation 30 .
  • This operation may be performed at a first station.
  • the reinforcement material 31 which has been given a shape corresponding to the shape of the door is applied to the vacuum-formed sheet at a second station.
  • the pre-forming of the reinforcements 31 may be done separately by means of stamping or by layer cutting or by some other previously disclosed method.
  • Hoses 32, 33 or similar are applied to the components in question at a third station.
  • a covering sheet 48' of the same nature as the bottom sheet is then positioned over the components and the hoses 32, 33 .
  • the top and bottom sheets are then welded or glued along their edges 39 .
  • the sheets are then stamped or cut in such a way that the unit in accordance with Figure 4c is produced.
  • the hose 33 is then connected to a vacuum pump 34 and the hose 32 is connected to a connector unit 35 for a nylon monomer containing an initiator and an activator.
  • the hoses 32, 33 are sealed, for example by welding, so that the cover formed by the top and the bottom sheets encloses the ingredients contained therein under essentially moisture-proof and, if necessary, air-evacuated conditions.
  • the sheet may simply be caused to weld together with the laminate contained inside it by raising the temperature during hardening to 200-220oC.
  • double sheets may be used, whereby the outer sheet shall exhibit a melting temperature in excess of the last-mentioned temperature.
  • the proportion of the reinforcement present may assume values of up to about 30 per cent by weight.
  • use may be made of long fibres, for example of glass, of about 25 cm in length or longer.
  • the arrangement or the semi-manufactured item may be given a lengthy storage capacity, for example several months, enabling the arrangement or the semi-manufactured item to be stored and handled under ordinary ambient temperature conditions. Finish-formed plastic material is conditioned so as to produce a certain amount of toughness in the material.
  • the present invention is not restricted to the embodiments specified above by way of example, but may undergo modifications within the context of the following Patent Claims and the idea of invention.

Landscapes

  • Engineering & Computer Science (AREA)
  • Chemical & Material Sciences (AREA)
  • Composite Materials (AREA)
  • Mechanical Engineering (AREA)
  • Textile Engineering (AREA)
  • Moulding By Coating Moulds (AREA)
  • Laminated Bodies (AREA)
  • Reinforced Plastic Materials (AREA)
  • Packging For Living Organisms, Food Or Medicinal Products That Are Sensitive To Environmental Conditiond (AREA)
  • Casting Or Compression Moulding Of Plastics Or The Like (AREA)
  • Buildings Adapted To Withstand Abnormal External Influences (AREA)
  • Cookers (AREA)
  • Processing And Handling Of Plastics And Other Materials For Molding In General (AREA)
EP84900317A 1982-12-23 1983-12-14 Anordnung, kunststoffingredienten und eine verstärkung enthaltend Withdrawn EP0131015A1 (de)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
SE8207378 1982-12-23
SE8207378 1982-12-23

Publications (1)

Publication Number Publication Date
EP0131015A1 true EP0131015A1 (de) 1985-01-16

Family

ID=20349131

Family Applications (2)

Application Number Title Priority Date Filing Date
EP84900316A Withdrawn EP0134218A1 (de) 1982-12-23 1983-12-14 Anordnung kunststoffkomponenten eingeschlossen in einem deckel enthaltend und deren herstellungsverfahren
EP84900317A Withdrawn EP0131015A1 (de) 1982-12-23 1983-12-14 Anordnung, kunststoffingredienten und eine verstärkung enthaltend

Family Applications Before (1)

Application Number Title Priority Date Filing Date
EP84900316A Withdrawn EP0134218A1 (de) 1982-12-23 1983-12-14 Anordnung kunststoffkomponenten eingeschlossen in einem deckel enthaltend und deren herstellungsverfahren

Country Status (11)

Country Link
EP (2) EP0134218A1 (de)
JP (2) JPS60500440A (de)
KR (1) KR840006930A (de)
ES (1) ES285338Y (de)
FI (1) FI843318A (de)
IL (1) IL70501A0 (de)
IT (2) IT1170063B (de)
NO (1) NO842890L (de)
OA (1) OA07785A (de)
WO (2) WO1984002490A1 (de)
ZA (1) ZA839492B (de)

Families Citing this family (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0549110A1 (de) * 1991-12-23 1993-06-30 Ford Motor Company Limited Verfahren zur Herstellung von faserverstärkten Artikeln
DE19814039A1 (de) * 1998-03-30 1999-10-07 Koegel Fahrzeugwerke Ag Sandwichelemente aus Kunststoff-Deckschichten und einem Kern zur Herstellung mobiler, temperaturgeführter Container
EP1156080A1 (de) * 2000-05-15 2001-11-21 Atofina Coextrudierter Film, enthaltend zwei äussere Lagen aus Polyamid oder Polyamid/Polyolefinlegierungen und eine Mittellage aus Polyolefin oder Polyamid oder Polyamid/Polyolefinlegierung
KR100537761B1 (ko) * 2002-10-25 2005-12-19 김수웅 거푸집용 코팅합판의 제조방법
EP1724098A1 (de) 2005-05-20 2006-11-22 Carbo Tech Composites GmbH Verfahren zur Herstellung eines laminierten Verbundwerkstoffprodukts und durch den Laminierungsverfahren hergestellter Verbundwerkstoff
EP2676780B1 (de) * 2012-06-18 2017-08-02 Technische Universität Dresden Verfahren zur Herstellung eines schichtförmigen Halbzeuges
JP6098483B2 (ja) * 2013-11-13 2017-03-22 トヨタ自動車株式会社 繊維強化樹脂材の製造方法
KR20190132364A (ko) 2017-02-08 2019-11-27 사이텍 인더스트리얼 머티어리얼즈(더비) 리미티드 복합 재료의 이중 다이어프램 성형, 이러한 성형을 위한 조립체 및 산출된 복합 재료

Family Cites Families (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CA575881A (en) * 1959-05-12 Scovill Manufacturing Company Check valve
US2588493A (en) * 1947-09-16 1952-03-11 Stefano John De Valve for stems of pneumatic tires
GB890304A (en) * 1959-07-23 1962-02-28 British Transp Commission Improvements relating to boards of resin-impregnated material
US3040764A (en) * 1960-07-20 1962-06-26 Alan R Feinberg Temperature and pressure relief valve
BE607271A (de) * 1960-08-17
EP0017452A1 (de) * 1979-03-30 1980-10-15 STOREY BROTHERS & COMPANY LIMITED Verfahren zur Herstellung eines gewölbten Körpers
AU532845B2 (en) * 1979-11-20 1983-10-13 Albert Fradin Moulding slow setting material

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
See references of WO8402491A1 *

Also Published As

Publication number Publication date
ES285338Y (es) 1986-12-01
EP0134218A1 (de) 1985-03-20
KR840006930A (ko) 1984-12-04
ES285338U (es) 1986-04-16
IT8324381A0 (it) 1983-12-23
IL70501A0 (en) 1984-03-30
WO1984002491A1 (en) 1984-07-05
FI843318A0 (fi) 1984-08-22
IT8324380A0 (it) 1983-12-23
JPS60500440A (ja) 1985-04-04
FI843318A (fi) 1984-08-22
OA07785A (en) 1986-11-20
ZA839492B (en) 1984-08-29
WO1984002490A1 (en) 1984-07-05
JPS60500284A (ja) 1985-03-07
NO842890L (no) 1984-07-13
IT1170063B (it) 1987-06-03
IT1170064B (it) 1987-06-03

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