GB2181998A - Method of providing a foamed mass in a hollow vehicle section - Google Patents

Method of providing a foamed mass in a hollow vehicle section Download PDF

Info

Publication number
GB2181998A
GB2181998A GB08619747A GB8619747A GB2181998A GB 2181998 A GB2181998 A GB 2181998A GB 08619747 A GB08619747 A GB 08619747A GB 8619747 A GB8619747 A GB 8619747A GB 2181998 A GB2181998 A GB 2181998A
Authority
GB
United Kingdom
Prior art keywords
composition
bag
cavity
foamed
polysiloxane
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.)
Granted
Application number
GB08619747A
Other versions
GB2181998B (en
GB8619747D0 (en
Inventor
Gareth Matthew Jones
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.)
Dow Silicones UK Ltd
Dow Silicones Corp
Original Assignee
Dow Corning Ltd
Dow Corning Corp
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 Dow Corning Ltd, Dow Corning Corp filed Critical Dow Corning Ltd
Publication of GB8619747D0 publication Critical patent/GB8619747D0/en
Priority to NL8602548A priority Critical patent/NL8602548A/en
Priority to IT21994/86A priority patent/IT1197836B/en
Priority to ES8602641A priority patent/ES2003886A6/en
Priority to SE8604481A priority patent/SE8604481L/en
Priority to FR8614649A priority patent/FR2592332A1/en
Priority to BE0/217319A priority patent/BE905637A/en
Priority to DE19863636113 priority patent/DE3636113A1/en
Publication of GB2181998A publication Critical patent/GB2181998A/en
Application granted granted Critical
Publication of GB2181998B publication Critical patent/GB2181998B/en
Expired 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
    • B29C44/12Incorporating or moulding on preformed parts, e.g. inserts or reinforcements
    • B29C44/18Filling preformed cavities
    • B29C44/182Filling flexible bags not having a particular shape
    • B29C44/184Filling flexible bags not having a particular shape and inserting the bags into preformed cavities
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B62LAND VEHICLES FOR TRAVELLING OTHERWISE THAN ON RAILS
    • B62DMOTOR VEHICLES; TRAILERS
    • B62D65/00Designing, manufacturing, e.g. assembling, facilitating disassembly, or structurally modifying motor vehicles or trailers, not otherwise provided for
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B29WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29KINDEXING SCHEME ASSOCIATED WITH SUBCLASSES B29B, B29C OR B29D, RELATING TO MOULDING MATERIALS OR TO MATERIALS FOR MOULDS, REINFORCEMENTS, FILLERS OR PREFORMED PARTS, e.g. INSERTS
    • B29K2083/00Use of polymers having silicon, with or without sulfur, nitrogen, oxygen, or carbon only, in the main chain, as moulding material
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B29WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29LINDEXING SCHEME ASSOCIATED WITH SUBCLASS B29C, RELATING TO PARTICULAR ARTICLES
    • B29L2031/00Other particular articles
    • B29L2031/30Vehicles, e.g. ships or aircraft, or body parts thereof

Landscapes

  • Engineering & Computer Science (AREA)
  • Manufacturing & Machinery (AREA)
  • Chemical & Material Sciences (AREA)
  • Combustion & Propulsion (AREA)
  • Transportation (AREA)
  • Mechanical Engineering (AREA)
  • Manufacture Of Porous Articles, And Recovery And Treatment Of Waste Products (AREA)
  • Casting Or Compression Moulding Of Plastics Or The Like (AREA)
  • Molding Of Porous Articles (AREA)

Abstract

A foamed mass is provided in a cavity of a hollow section of a vehicle body using a room temperature curable foam forming silicone composition. Flow of the composition as it foams and cures is restricted by a bag. The bag is inserted in the cavity and the composition introduced to the bag in liquid form. The composition is held in the bag and the composition expands therein and the bag is urged into conformity with the shape of the cavity. By this means inhibition of the cure of the silicone composition by materials in the section is prevented, and the composition is held in place until it has cured so that even heightwise disposed sections with open ended cavities may be satisfactorily treated. The bag remains as a sheath for the cured foam and serves to isolate the mass from its environment.

Description

SPECIFICATION Method of providing a foamed mass in a cavity This invention is concerned with a method of providing a foamed mass in a cavity.
In the manufacture of vehicle bodies including a hollow section, for example of metal, it is sometimes desired to include within the hollow section a material intended to contribute sound deadening, flame retardant or other properties. The shape, size and disposition of those cavities within the hollow section into which the material is to be placed may render the use of blocks e.g. of preformed foam inappropriate. In those cases where it is desired to fill a cavity having a complex shape or one of non-uniform cross section on a production line basis it is likely to be appropriate to introduce to the cavity a liquid material which flows to the desired shape and then hardens or cures to provide a suitable filling. In those cases where light weight or sound deadening properties are desired, it is appropriate to employ a material which also foams when introduced to the cavity.For the avoidance of corrosion of metal sections it is desirable to employ as the material a product which does not encourage corrosion of metal sections or other degradation of items within the section, for example wires or sheathed cables, and equally it is desirable to employ as the material a product which is not adversely affected by other materials present within the hollow section for example waxes, drawing oils, wires and sheaths of cables.
These and other requirements have restricted the choice of materials which may be employed.
Liquid, foam forming, curable compositions based on silicone materials are available which flow and foam readily at room or sightly elevated temperatures to provide a cured product which is light in weight, and has sound absorbing and heat resistant properties and may also have flame retardant properties. Known compositions generally require several minutes to cure to a selfsupporting condition. When these compositions are used within hollow metal sections in contact therewith, the cure may be inhibited due, for example, to the influence of materials within the section upon catalysts used in the composition and so the cure within hollow metal sections may require a significant period.Attempts to use such compositions for filling hollow sections which have significant openings at their lower ends are thus frustrated by flow of composition from the opening before the composition becomes sufficiently cured to be self-supporting.
Whilst it is possible to dam the flow in some cases, this is not always conveniently achieved, and also does not remove difficulties associated with inhibition of the cure.
We have now found that a liquid, foam forming, ambient temperature curable, silicone based composition may be filled rapidly into a cavity in a hollow section of a vehicle body without undesirable loss of the fluid from openings in the section, to provide a cured foam filling if there is first inserted into the hollow section a bag which serves to restrict flow of the liquid composition within the hollow section, is capable of being urged into conformity with the surface of the cavity by the composition as it foams and thereafter serves as a sheath for the cured foam.
The invention provides in one of its aspects a method of providing a foamed mass within a cavity in a section of a vehicle body comprising the steps of introducing to the cavity a bag of flexible material and introducing into the bag a liquid, foam forming, curable silicone composition capable of curing to a foamed elastomeric mass at ambient temperatures, the bag and composition being so chosen that the bag is urged into conformity with the shape of the cavity by the composition as it foams.
In a method according to the invention the bag serves to provide a membrane in the cavity to limit flow of the liquid composition, to provide a container for the composition as it is converted to its cured condition to provide a barrier between the foamable composition and any cure inhibiting substances that may be present in the cavity and to provide a membrane or sheath for the cured foam disposed between the composition and the cavity walls. The bag is chosen so that it may have a perimeter not smaller than the perimeter of a cross section of the cavity to be filled and so that it is flexible enough to be spread out and pressed by the expanding foam into conformity with walls of the cavity.The bag may be of a material which is elastic, inelastic or capable of being enlarged under the influence of the foaming composition but should not act to reduce the volume of the foam after the foam has cured to the shape of the cavity. A method according to the invention may be used to fill or partially fill hollow sections of various sizes and dispositions in vehicle bodies and is principally intended for use in the filling or blocking of hollow sections of vehicles for sound deadening purposes and for restriction of ingress of unwanted materials during use of the vehicle.When using a method according to the invention to block a cavity in a widthwise extending hollow section the bag may be selected to restrict outward flow of the composition whilst permitting heightwise expansion of the foaming composition to urge the bag into conformity with the downward facing interior of the cavity.
When using a method according to the invention to block a cavity in a heightwise extending hollow section the bag may be selected to restrict downward flow of the composition whilst permitting widthwise expansion of the foaming mass to urge the bag into conformity with the interior of the cavity.
The mouth of the bag may be closed before the curing reaction is complete, so that the cured foam is totally enclosed by the bag and this may be particularly advantageous in those cases where it is desired to form a short barrier across a hollow section, or to separate the composition from the surroundings. Alternatively, the foamed mass may be permitted to extend beyond the open mouth of the bag, for example in those cases where it is desirable or permissible for the foamed mass to extend from the hollow section. Materials suitable for providing the bag are those which do not deleteriously influence the curable composition, and which are able to provide bag walls which are sufficiently cohesive to hold the foam as it forms and are flexible enough to allow the bag to be opened out by pressure from the foaming mass and pressed into conformity with the cavity.Bags which are impervious to the curable composition are preferred.
Suitable materials include flexible plastics materials for example polyethylene and cellophane.
Particularly suitable are bags formed from a tubular extrusion of polyethylene about 0.003mm to about 0.015mm thick.
In a method according to the invention, a liquid foam forming, curable silicone composition is used. The composition chosen is one which is curable at ambient temperature i.e. the temperature in the hollow section at the time of installation which may be in the range from about 1 50C to about 300C for example. Materials which require significant application of heat in order to effect cure in an acceptable period of time impose additional limitations on various aspects of the method, including the choice of a suitable heat resistant material for the bag.
Room temperature curable compositions which foam by virtue of in situ production of gases during curing are particularly preferred. The curable silicone compositions preferably comprise a polysiloxane having alkylhydrogen-siloxane units and a hydroxylated material so that the composition is curable to form a polysiloxane matrix which is foamed by evolution of hydrogen gas under the influence of a suitable catalyst (for example a tin salt of a carboxylic acid as referred to in G.B. Patent Specification 798 669 or a platinum catalyst as referred to in G.B. Patent Specification 1 522 637) according to the schemesSiH+HOQ ,eSiOQ+H2 as is known in the art. For example curable, foam forming silicone compositions are disclosed in G.B. Patent Specifications 798 669, 867 619 and 1 522 637.Hydrogen gas generated during the reaction causes foaming and expansion of the composition as it cures, resulting in an outward pressure from the composition exerted upon the bag. If desired, foaming of the composition and thus the pressure to expand the bag may be augmented for example by use of additional foaming agent, for example compressed air, nitrogen and the liquefied gases known for use in aerosols, including hydrocarbons, for example methane, ethylene, ethane, propane, neopentane and the many fluorinated hydrocarbons for example methyl fluoride, trifluoromethane, monochlorodifluoromethane and dichlorodifluoromethane. The hydroxylated material (QOH) may be an organic material or a silicon compound and preferably comprises two or more hydroxyl groups per molecule in order to provide a suitable elastomeric foam mass.Preferably the hydroxylated material comprises a polysiloxane having silicon-bonded hydroxyl groups. If desired one may also include in the composition a polysiloxane having alkenyl e.g. vinyl groups, which is particularly beneficial if a platinum catalyst is employed for the addition reaction between the alkylhydrogensiloxane and alkenyl groups, due to flame retardant properties conferred by the platinum compound.
Suitable polysiloxanes having alkylhydrogensiloxane units include polymers having units according to the general formula RpHS#0(3#p) 2 in which each R represents a lower alkyl or phenyl group e.g. a methyl group, and p is 1 or 2.
The alkylhydrogen polysiloxanes may also comprise units RnSiO4-n 2 in which R is as referred to above and n is 1, 2 or 3. Curing reactions of the preferred compositions are dependant on presence of appropriate quantities of the interactive functionalities and the alkylhydrogen polysiloxane may be selected accordingly. We prefer that each R represents a methyl group. Preferably terminal groups of the alkylhydrogen polysiloxane have the formula R3SiOI where each R represents a methyl group. Suitable alkylhydrogen polysiloxanes include those comprising MeHSiO units with or without the presence of Me2SiO units and having viscosities of the order of from about 10-6 to about 10-4 m2/s more preferably from about 10-6 to about 5x10-5 m2/s.
Suitable polysiloxanes having silicon-bonded hydroxyl or alkenyl groups include polymers which include units according to the general formula Rm(Q)SiO3-m 2 in which each Q represents an OH group or an alkenyl group having 2 to 4 carbon atoms inclusive, for example a -CH=CH2 or a -CH2-CH=CH2 group, each R represents a lower alkyl or phenyl radical e.g. a methyl radical and m is 1 or 2. These polysiloxanes also comprise units RnSiO4-n 2 in which R and n are as referred to above. These materials are preferably liquids and are chosen so that their functionality is appropriate in relation to the degree of chain extension and crosslinking required during curing of the composition.The polysiloxanes having silicon-bonded hydroxyl groups are preferably silanol terminated polydiorganosiloxanes according to the general formula
in which each R represents a methyl group and n has a value such that the polysiloxane has a viscosity of about 5x10--4 to 2.5x to2.5 > < 10-2 m2/s i.e. a number average molecular weight of the order of about 20,000 to about 80,000. Preferred materials have viscosities of the order of about 1.5x103 to about 1.5x102 m2/s and comprise, per molecule, primarily units according to the general formula R2SiO and two units according to the general formula R2(0H)Si01. Preferred polysiloxanes having silicon-bonded alkenyl groups include those in which the alkenyl groups provide less than about 5% of the total silicon-bonded organic groups of the polymer.The alkenyl groups may be attached to terminal silicon atoms of the polysiloxane chain or to silicon atoms along the chain or both. Suitable alkenyl polysiloxanes include dimethylvinyl end blocked polysiloxanes for example those having viscosities up to about 8.5 x 10- 2 m2/s and phenylmethylvinyl end blocked polydimethylsiloxanes for example those having viscosities of about 2.5x 10-4 to about 102 to about 10 2 m2/s. In the preferred materials, each R represents a methyl radical. In preferred compositions according to the invention, the preferred hydroxy and alkenyl functional polysiloxanes thus provide polysiloxane chains of significant length and this is desirable in view of flexibility and elastomeric properties required of the product resulting from curing of the composition.If desired, comparatively low molecular weight, i.e. short chained, organodifunctional polysiloxanes may also be included in the composition. Suitable materials include a,w, dihydroxy polydimethylsiloxanes having up to twenty five dimethylsiloxane units in the molecular chain.
One may also include in the composition appropriate quantities of higher functional materials as crosslinking agents. Suitable crosslinking agents include materials having three or more functional e.g. hydroxy groups per molecule. Preferred crosslinking agents include an alkoxysilane and/or a condensation product thereof capable of combining with three or more hydroxy polysiloxane molecules with release of the corresponding alcohol of the alkyl radicals, e.g. methyl trimethoxysilane, n-propylorthosilicate and ethyl polysilicate.
Compositions for use in the invention preferably include monofunctional hydroxy silicon compounds effective as chain terminators. Such materials influence the structure of foams formed by use of the composition and their use is highly preferred where predominantly open-celled foams are desired. Suitable monofunctional hydroxy compounds include triorganosilanols and organosiloxanols which may be for example short chain siloxanes having for example up to about 25 siloxane units per molecule and having a terminal or pendant hydroxyl group, or a material of the general formula R3SiOH where each R may be for example a lower alkyl group e.g. a methyl group or a phenyl group. Examples of such materials include
(nonamethyltetrasiloxan- 1 -ol) (heptamethyltrisiloxan-2-ol) and (diphenylmethylsilanol) Preferably fillers are incorporated in compositions used in the invention.Any desired filler may be employed for example metal oxides, clays, fume silicas, hydrophobic silicas e.g. those prepared by treatment of finely divided silica with organochlorosilanes, organosiloxanes, organosilazanes or alkylsilanols and powdered glass.
Advantages which flow from use of the invention stem primarily from the control of flow of the composition before it has cured to a self supporting condition and from the separation of the composition and hollow section by means of the bag. Thus one may, for example, apply a prescribed quantity of composition to a heightwise extending hollow section without the composition flowing from the section before it cures. One may disregard the possibility of inhibiting the cure of the composition and other deleterious effects which may be caused by materials of or on the hollow section. Equally, one may employ a composition which, in the absence of the bag, might bring about unwanted effects on the hollow section or its other contents.Furthermore one may achieve repetitively uniform filling of cavities in hollow sections with minimal operator attention after introduction of the bag and the liquid composition to the cavity. Further advantages achieved by use of the invention include an improved resistance to moisture transmission via the foam when a moisture impervious bag is used.
A method according to the invention may be employed for the partial or complete filling of cavities in hollow sections of vehicle bodies and is principally of value in the sound deadening of cars and vans which have substantial lengths of open-ended tubular sections. It is of value primarily in those situations where it is important to minimise wastage of material from heightwise extending hollow sections or to ensure satisfactory results without prolonged attention by operatives. Thus it is envisaged as of particular value in the manufacture of vehicles on a production line basis, for example in the treatment of door pillars, "A posts" and the like.
In order that the invention may become more clear, there now follows a description of example method according to the invention and illustrative thereof.
In the example methods the following liquid, foam forming, curable compositions A and B based on silicone materials were used. Compositions A was a two part room temperature curable silicone composition formed by mixing in equal volumes Parts 1 and 2 composed of the following materials.
Material Parts by Weight Part 1 Part 2 a, hydroxypolydimethylsiloxane viscosity about 1.35 x 10-2 m2/s 22 30 a hydroxypolydimethylsiloxane viscosity about 4.2x 10-5 m2/s - 6 Trimethylsiloxy end-blocked polymethyl hydrogensiloxane, viscosity 3 x 10-5 m2/s - 4 Copolymer of polydimethyl and polymethyl hydrogen siloxanes of viscosity 5x10-6 m2/s 1 Dimethylvinyl end-blocked polydimethyl siloxane of viscosity 4.5 x 10-4 m2/s 17 Methylvinyl cyclic polysiloxane - .04 Silica filler 8 8 Platinum catalyst compound 0.25 Pigment 2.8 When mixed, the composition foamed and cured at room temperature to provide a medium density (about 170 to 220 kg/m3) foam having for example good heat resistant, thermal insulation and sound insulation properties.
Composition B was a two part room temperature curable silicone composition formed by mixing 7 parts by weight stannous octoate with a composition comprising Material Parts by Weight a,w, hydroxypolydimethylsiloxane MW about 21,000 (viscosity about 2x 10-3 m2/s) 100 or,~, hydroxypolydimethylsiloxane MW about 900 (viscosity about 4.2 x 10-5 m2/s) 10 Diphenylmethylsilanol 10 Trimethylsiloxy endblocked methyl hydrogensiloxane, (viscosity about 3x10-5 m2/s) 10 Finely divided filler 25 n-propylorthosilicate 4 When mixed, the composition foamed and cured at room temperature to provide a low density (about 120 to 200 kg/m3) foam having for example good sound insulation properties.
Example 1 A bag formed from a tube of circumference 230mm of polyethylene film 0.006mm thick sealed at one end to form a rectangular bag closed at three of its edges and having a width of 115mm was placed in a 250ml beaker (circumference 203mm, radius 32.3mm and height 77mm) with its open mouth at the mouth of the beaker. Composition A was mixed and poured into the bag in the flask. The composition foamed, pressed the bag firmly against the inner wall of the beaker and cured to a medium density in the bag. Observations revealed no evidence of inhibition of the cure due to the polyethylene. Similar results were obtained when composition B was used instead of composition A.
Example 2 A bag formed from a tube of 280mm circumference of polyethylene film 0.006mm thick sealed at one end to form a rectangular bag closed at three of its edges and having a width of 140mm was placed in a rectangular transparent Perspex tube having a cross section of 76.2mm x 50.8mm and a height of 200mm. The Perspex tube was open at both ends. The tube was placed with the length of its cavity extending heightwise and the bag was placed in the upper half of the tube with the mouth of the bag adjacent the upper opening of the Perspex tube. Composition A was mixed and poured into the mouth of the bag, sufficient mixed composition being used to ensure the foam produced extended above the mouth of the bag. A lower surface of the bag prevented downward flow of the composition from the bag.The composition foamed, pressing the bag into conformity with the shape of the rectangular tube and cured to trap the bag against the interior walls of the Perspex tube.
Example 3 A Perspex tube as described in Example 2 but having a lOmm diameter hole cut in one wall approximately 100mm from the lower end of the tube was employed. A bag formed from a tube of 330mm circumference of polyethylene film 0.006mm thick sealed at one end to form a rectangular bag closed at three of its edges was inserted in the Perspex tube via the hole. The mouth of the bag was retained on the outside of the Perspex tube. Composition B was mixed and injected through the mouth of the bag to the interior of the bag. The composition foamed, and as it expanded, the bag was urged into conformity with the cavity in the tube and along the tube to an extent permitted by the bag. The composition cured to provide a foam mass trapping the bag against the interior of the tube to effect sealing of the tube.
Example 4 In this Example a cavity in a vertical door pillar of a car body was filled with a foamed mass during manufacture of the car. The door pillar was of conventional construction and presented a hollow section of a generally rectangular shaped cross section of perimeter about 150mm which was open at its base. The hollow section contained a wiring harness comprising pvc coated wires and residue of the usual drawing oils and other contaminants. A bag 200mm long and as used in Example 3 was introduced to the cavity defined by the interior surfaces of the hollow section and exterior surfaces of the wiring harness via a hole in the pillar. The mouth of the bag was retained outside the pillar. Composition B was mixed and injected through the mouth of the bag into the cavity. The composition flowed downward in the bag in the cavity to an extent permitted by the bag and foamed and cured to block the pillar, with the bag trapped by the cured foam against the pillar walls and wiring harness. The mouth of the bag was trimmed off.

Claims (9)

1. A method of providing a foamed mass within a cavity in a section of a vehicle body comprising the steps of introducing to the cavity a bag of flexible material and introducing into the bag a liquid, foam forming, curable silicone composition capable of curing to a foamed elastomeric mass at ambient temperatures, the bag and composition being so chosen that the bag is urged into conformity with the shape of the cavity by the composition as it foams.
2. A method according to Claim 1 wherein the composition comprises a polysiloxane having alkylhydrogensiloxane units, a hydroxylated material and a catalyst.
3. A method according to Claim 2 wherein the hydroxylated material comprises a polysiloxane having silicon-bonded hydroxyl groups.
4. A method according to Claim 3 wherein the catalyst comprises a tin salt of a carboxylic acid.
5. A method according to either one of Claims 2 and 3 wherein the composition also comprises a polysiloxane having silicon-bonded alkenyl groups and the catalyst comprises a platinum compound.
6. A method according to Claim 1 wherein the composition is substantially as hereinbefore described, particularly with reference to composition A or composition B.
7. A method according to any one of the preceding claims wherein the bag is formed from polyethylene film having a thickness from about 0.003mm to 0.015mm.
8. A method according to Claim 1 substantially as hereinbefore described with reference to any one of the examples.
9. A vehicle body having a hollow section containing a foamed composition provided by a method according to any one of the preceding claims.
GB08619747A 1985-10-24 1986-08-13 Method of providing a foamed mass in a cavity in a vehicle body Expired GB2181998B (en)

Priority Applications (7)

Application Number Priority Date Filing Date Title
NL8602548A NL8602548A (en) 1985-10-24 1986-10-10 METHOD FOR PROVIDING A FOAMED MASS IN A CAVITY
IT21994/86A IT1197836B (en) 1985-10-24 1986-10-14 METHOD FOR MAKING A FOAM MASS INSIDE A CAVITY
ES8602641A ES2003886A6 (en) 1985-10-24 1986-10-17 Process for forming an alveolate mass in a cavity by expansion of a silicone composition introduced in a bag placed in the cavity
SE8604481A SE8604481L (en) 1985-10-24 1986-10-21 WAY TO arrange an expanded mass in a room
FR8614649A FR2592332A1 (en) 1985-10-24 1986-10-22 Process for forming an alveolate mass in a cavity by expansion of a silicone composition introduced in a bag placed in the cavity
BE0/217319A BE905637A (en) 1985-10-24 1986-10-22 PROCESS FOR FORMING A MASS OF FOAM IN A CAVITY.
DE19863636113 DE3636113A1 (en) 1985-10-24 1986-10-23 METHOD FOR FORMING A FOAMED DIMENSION IN A CAVITY

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB858526292A GB8526292D0 (en) 1985-10-24 1985-10-24 Foam filled elements

Publications (3)

Publication Number Publication Date
GB8619747D0 GB8619747D0 (en) 1986-09-24
GB2181998A true GB2181998A (en) 1987-05-07
GB2181998B GB2181998B (en) 1988-12-21

Family

ID=10587214

Family Applications (2)

Application Number Title Priority Date Filing Date
GB858526292A Pending GB8526292D0 (en) 1985-10-24 1985-10-24 Foam filled elements
GB08619747A Expired GB2181998B (en) 1985-10-24 1986-08-13 Method of providing a foamed mass in a cavity in a vehicle body

Family Applications Before (1)

Application Number Title Priority Date Filing Date
GB858526292A Pending GB8526292D0 (en) 1985-10-24 1985-10-24 Foam filled elements

Country Status (3)

Country Link
JP (1) JPS62119011A (en)
GB (2) GB8526292D0 (en)
ZA (1) ZA866939B (en)

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE3838655A1 (en) * 1988-11-15 1990-05-17 Bayerische Motoren Werke Ag Process and apparatus for filling vehicle body cavities with foam
WO1995025005A1 (en) * 1994-03-14 1995-09-21 Ymos Aktiengesellschaft Industrieprodukte Composite material with foamable core
EP1389604A1 (en) * 2001-05-23 2004-02-18 Bridgestone Corporation BAG CAPABLE OF PREVENTING PERMEATION OF LIQUID&comma; CUSHION AND CLEARANCE FILLING STRUCTURE
EP1426273A2 (en) * 2002-12-02 2004-06-09 ArvinMeritor Technology, LLC A reinforced structural member

Cited By (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE3838655A1 (en) * 1988-11-15 1990-05-17 Bayerische Motoren Werke Ag Process and apparatus for filling vehicle body cavities with foam
WO1995025005A1 (en) * 1994-03-14 1995-09-21 Ymos Aktiengesellschaft Industrieprodukte Composite material with foamable core
EP0679501A1 (en) * 1994-03-14 1995-11-02 YMOS AKTIENGESELLSCHAFT Industrieprodukte Composite material with foamable core
US5766719A (en) * 1994-03-14 1998-06-16 Magna Exterior Systems Gmbh Composite material
EP1389604A1 (en) * 2001-05-23 2004-02-18 Bridgestone Corporation BAG CAPABLE OF PREVENTING PERMEATION OF LIQUID&comma; CUSHION AND CLEARANCE FILLING STRUCTURE
EP1389604A4 (en) * 2001-05-23 2004-09-29 Bridgestone Corp Bag capable of preventing permeation of liquid, cushion and clearance filling structure
EP1426273A2 (en) * 2002-12-02 2004-06-09 ArvinMeritor Technology, LLC A reinforced structural member
EP1426273A3 (en) * 2002-12-02 2004-07-28 ArvinMeritor Technology, LLC A reinforced structural member
US7341317B2 (en) 2002-12-02 2008-03-11 Arvinmeritor Technology, Llc Locally reinforced hollow structural assembly

Also Published As

Publication number Publication date
ZA866939B (en) 1987-04-29
JPH0318807B2 (en) 1991-03-13
GB2181998B (en) 1988-12-21
JPS62119011A (en) 1987-05-30
GB8526292D0 (en) 1985-11-27
GB8619747D0 (en) 1986-09-24

Similar Documents

Publication Publication Date Title
FI66896C (en) FOERFARANDE FOER FRAMSTAELLNING AV ORGANOPOLYSILOXANFORMMASSORAV VILKA ERHAOLLES FINPORIGA GUMMIELASTISKA FORMSKUMKROPP AR
Warrick et al. Silicone elastomer developments 1967–1977
US5162397A (en) Silicone foams
CA1270096A (en) Lower density silicone elastomeric foam
US4802068A (en) Sealed chambers
JPS62114560A (en) Production of cover material
KR100890599B1 (en) Microwave foam
CA1302217C (en) Method of providing a foamed mass in a cavity
CA1274947A (en) Organosiloxane foams
CA2344941A1 (en) Silicone rubber sponge composition, sponge, and process for making
JPH036175B2 (en)
GB2181998A (en) Method of providing a foamed mass in a hollow vehicle section
US5051224A (en) Method for molding composite articles
NL8602548A (en) METHOD FOR PROVIDING A FOAMED MASS IN A CAVITY
EP0338693A2 (en) Method for making silicone foam masses
EP0291197B1 (en) Non-settling foams
KR20010092410A (en) Silicone rubber sponge composition and sponge articles therefrom
JPH11130963A (en) Expandable polyorganosiloxane composition and foam
JP2563155B2 (en) Flame-retardant coated heat-insulating pipe, heat-insulating coated pipe used therefor, and method for producing the same
US4567212A (en) Nonslumping, foamable polyorganosiloxane compositions containing organosiloxane graft copolymers
US4973642A (en) High temperature crumb rubber for use in composite manufacture
US5126083A (en) Silicone foams of improved fire resistance
US4552901A (en) Nonslumping, foamable polyorganosiloxane compositions containing organosiloxane graft copolymers
EP0287230A2 (en) Method of providing a foamed mass in a cavity
JPH0344577B2 (en)

Legal Events

Date Code Title Description
PCNP Patent ceased through non-payment of renewal fee