EP0148885A1 - Materiaux composites a zones de raidissement - Google Patents
Materiaux composites a zones de raidissementInfo
- Publication number
- EP0148885A1 EP0148885A1 EP84902524A EP84902524A EP0148885A1 EP 0148885 A1 EP0148885 A1 EP 0148885A1 EP 84902524 A EP84902524 A EP 84902524A EP 84902524 A EP84902524 A EP 84902524A EP 0148885 A1 EP0148885 A1 EP 0148885A1
- Authority
- EP
- European Patent Office
- Prior art keywords
- stiffening
- fibres
- stiffening material
- composite article
- elastomeric matrix
- 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- Withdrawn
Links
- 239000002131 composite material Substances 0.000 title claims abstract description 38
- 239000000463 material Substances 0.000 claims abstract description 60
- 239000011159 matrix material Substances 0.000 claims abstract description 57
- 238000010168 coupling process Methods 0.000 claims abstract description 31
- 238000005859 coupling reaction Methods 0.000 claims abstract description 31
- 230000008878 coupling Effects 0.000 claims abstract description 29
- 230000007704 transition Effects 0.000 claims abstract description 21
- 229920000647 polyepoxide Polymers 0.000 claims description 31
- 239000003822 epoxy resin Substances 0.000 claims description 29
- JOYRKODLDBILNP-UHFFFAOYSA-N Ethyl urethane Chemical compound CCOC(N)=O JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 claims description 28
- 230000003014 reinforcing effect Effects 0.000 claims description 28
- 229920000728 polyester Polymers 0.000 claims description 9
- KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical compound C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 claims description 8
- 229910052799 carbon Inorganic materials 0.000 claims description 8
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 7
- 239000004642 Polyimide Substances 0.000 claims description 6
- 239000004645 polyester resin Substances 0.000 claims description 6
- 229920001225 polyester resin Polymers 0.000 claims description 6
- 229920001721 polyimide Polymers 0.000 claims description 6
- 229920001971 elastomer Polymers 0.000 claims description 5
- 239000000806 elastomer Substances 0.000 claims description 5
- 239000011521 glass Substances 0.000 claims description 5
- LNEPOXFFQSENCJ-UHFFFAOYSA-N haloperidol Chemical compound C1CC(O)(C=2C=CC(Cl)=CC=2)CCN1CCCC(=O)C1=CC=C(F)C=C1 LNEPOXFFQSENCJ-UHFFFAOYSA-N 0.000 claims description 5
- -1 polyethylene, ethylene propylene Polymers 0.000 claims description 5
- 229920002635 polyurethane Polymers 0.000 claims description 5
- 239000004814 polyurethane Substances 0.000 claims description 5
- ZOXJGFHDIHLPTG-UHFFFAOYSA-N Boron Chemical compound [B] ZOXJGFHDIHLPTG-UHFFFAOYSA-N 0.000 claims description 4
- 239000004677 Nylon Substances 0.000 claims description 4
- 239000004760 aramid Substances 0.000 claims description 4
- 229920003235 aromatic polyamide Polymers 0.000 claims description 4
- 229910052796 boron Inorganic materials 0.000 claims description 4
- 239000002184 metal Substances 0.000 claims description 4
- 229910052751 metal Inorganic materials 0.000 claims description 4
- 229920001778 nylon Polymers 0.000 claims description 4
- 230000002787 reinforcement Effects 0.000 claims description 4
- 239000000203 mixture Substances 0.000 claims description 3
- 239000005011 phenolic resin Substances 0.000 claims description 3
- 229920001568 phenolic resin Polymers 0.000 claims description 3
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 claims description 3
- 239000004709 Chlorinated polyethylene Substances 0.000 claims description 2
- BRLQWZUYTZBJKN-UHFFFAOYSA-N Epichlorohydrin Chemical compound ClCC1CO1 BRLQWZUYTZBJKN-UHFFFAOYSA-N 0.000 claims description 2
- 244000043261 Hevea brasiliensis Species 0.000 claims description 2
- VHOQXEIFYTTXJU-UHFFFAOYSA-N Isobutylene-isoprene copolymer Chemical compound CC(C)=C.CC(=C)C=C VHOQXEIFYTTXJU-UHFFFAOYSA-N 0.000 claims description 2
- 239000004952 Polyamide Substances 0.000 claims description 2
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Natural products C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 claims description 2
- 239000002174 Styrene-butadiene Substances 0.000 claims description 2
- 150000001336 alkenes Chemical class 0.000 claims description 2
- MTAZNLWOLGHBHU-UHFFFAOYSA-N butadiene-styrene rubber Chemical compound C=CC=C.C=CC1=CC=CC=C1 MTAZNLWOLGHBHU-UHFFFAOYSA-N 0.000 claims description 2
- YACLQRRMGMJLJV-UHFFFAOYSA-N chloroprene Chemical compound ClC(=C)C=C YACLQRRMGMJLJV-UHFFFAOYSA-N 0.000 claims description 2
- 229920001577 copolymer Polymers 0.000 claims description 2
- 150000002739 metals Chemical class 0.000 claims description 2
- 229920003052 natural elastomer Polymers 0.000 claims description 2
- 229920001194 natural rubber Polymers 0.000 claims description 2
- 150000002825 nitriles Chemical class 0.000 claims description 2
- 229920002647 polyamide Polymers 0.000 claims description 2
- 229920002379 silicone rubber Polymers 0.000 claims description 2
- 239000011115 styrene butadiene Substances 0.000 claims description 2
- 229920003048 styrene butadiene rubber Polymers 0.000 claims description 2
- 229920001567 vinyl ester resin Polymers 0.000 claims description 2
- 229920001195 polyisoprene Polymers 0.000 claims 1
- 239000000126 substance Substances 0.000 abstract description 5
- 239000012783 reinforcing fiber Substances 0.000 abstract 2
- 229960005088 urethane Drugs 0.000 description 26
- 239000000835 fiber Substances 0.000 description 22
- 229920002803 thermoplastic polyurethane Polymers 0.000 description 20
- 206010052904 Musculoskeletal stiffness Diseases 0.000 description 18
- 229920005989 resin Polymers 0.000 description 18
- 239000011347 resin Substances 0.000 description 18
- 238000013461 design Methods 0.000 description 12
- 230000033001 locomotion Effects 0.000 description 12
- 239000003795 chemical substances by application Substances 0.000 description 8
- 230000005540 biological transmission Effects 0.000 description 7
- 238000010276 construction Methods 0.000 description 7
- 238000009826 distribution Methods 0.000 description 6
- 238000000034 method Methods 0.000 description 6
- 238000005452 bending Methods 0.000 description 5
- 150000002924 oxiranes Chemical class 0.000 description 5
- 238000009954 braiding Methods 0.000 description 4
- 125000004122 cyclic group Chemical group 0.000 description 4
- 239000004744 fabric Substances 0.000 description 4
- 238000011065 in-situ storage Methods 0.000 description 4
- 238000002347 injection Methods 0.000 description 4
- 239000007924 injection Substances 0.000 description 4
- 229920000271 Kevlar® Polymers 0.000 description 3
- 229910000831 Steel Inorganic materials 0.000 description 3
- 238000004132 cross linking Methods 0.000 description 3
- 238000013016 damping Methods 0.000 description 3
- 150000004985 diamines Chemical class 0.000 description 3
- 238000009730 filament winding Methods 0.000 description 3
- 239000004761 kevlar Substances 0.000 description 3
- 238000004519 manufacturing process Methods 0.000 description 3
- 239000010959 steel Substances 0.000 description 3
- 238000012546 transfer Methods 0.000 description 3
- 238000004804 winding Methods 0.000 description 3
- 229920002430 Fibre-reinforced plastic Polymers 0.000 description 2
- 238000004026 adhesive bonding Methods 0.000 description 2
- 238000010382 chemical cross-linking Methods 0.000 description 2
- 230000007797 corrosion Effects 0.000 description 2
- 238000005260 corrosion Methods 0.000 description 2
- 239000011151 fibre-reinforced plastic Substances 0.000 description 2
- 239000006260 foam Substances 0.000 description 2
- 238000000465 moulding Methods 0.000 description 2
- 239000012466 permeate Substances 0.000 description 2
- 239000003351 stiffener Substances 0.000 description 2
- 238000006467 substitution reaction Methods 0.000 description 2
- 229920001187 thermosetting polymer Polymers 0.000 description 2
- 150000003673 urethanes Chemical class 0.000 description 2
- 229930185605 Bisphenol Natural products 0.000 description 1
- 101100536354 Drosophila melanogaster tant gene Proteins 0.000 description 1
- 239000004593 Epoxy Substances 0.000 description 1
- 229910001209 Low-carbon steel Inorganic materials 0.000 description 1
- 239000004698 Polyethylene Substances 0.000 description 1
- 239000006096 absorbing agent Substances 0.000 description 1
- 230000009471 action Effects 0.000 description 1
- 230000001154 acute effect Effects 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 229920005549 butyl rubber Polymers 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 230000032798 delamination Effects 0.000 description 1
- 238000006073 displacement reaction Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 239000013536 elastomeric material Substances 0.000 description 1
- 238000009787 hand lay-up Methods 0.000 description 1
- 238000010348 incorporation Methods 0.000 description 1
- 230000002401 inhibitory effect Effects 0.000 description 1
- 230000000977 initiatory effect Effects 0.000 description 1
- 238000001746 injection moulding Methods 0.000 description 1
- 238000003780 insertion Methods 0.000 description 1
- 230000037431 insertion Effects 0.000 description 1
- 238000009940 knitting Methods 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 229920001084 poly(chloroprene) Polymers 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 239000004848 polyfunctional curative Substances 0.000 description 1
- 229920001228 polyisocyanate Polymers 0.000 description 1
- 239000005056 polyisocyanate Substances 0.000 description 1
- 230000008569 process Effects 0.000 description 1
- 238000005096 rolling process Methods 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 238000010008 shearing Methods 0.000 description 1
- 230000035939 shock Effects 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 229920002554 vinyl polymer Polymers 0.000 description 1
Classifications
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B60—VEHICLES IN GENERAL
- B60B—VEHICLE WHEELS; CASTORS; AXLES FOR WHEELS OR CASTORS; INCREASING WHEEL ADHESION
- B60B5/00—Wheels, spokes, disc bodies, rims, hubs, wholly or predominantly made of non-metallic material
- B60B5/02—Wheels, spokes, disc bodies, rims, hubs, wholly or predominantly made of non-metallic material made of synthetic material
-
- 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
- B29C70/00—Shaping composites, i.e. plastics material comprising reinforcements, fillers or preformed parts, e.g. inserts
- B29C70/04—Shaping composites, i.e. plastics material comprising reinforcements, fillers or preformed parts, e.g. inserts comprising reinforcements only, e.g. self-reinforcing plastics
- B29C70/06—Fibrous reinforcements only
- B29C70/08—Fibrous reinforcements only comprising combinations of different forms of fibrous reinforcements incorporated in matrix material, forming one or more layers, and with or without non-reinforced layers
-
- 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
- B29C70/00—Shaping composites, i.e. plastics material comprising reinforcements, fillers or preformed parts, e.g. inserts
- B29C70/04—Shaping composites, i.e. plastics material comprising reinforcements, fillers or preformed parts, e.g. inserts comprising reinforcements only, e.g. self-reinforcing plastics
- B29C70/28—Shaping operations therefor
- B29C70/40—Shaping or impregnating by compression not applied
- B29C70/42—Shaping or impregnating by compression not applied for producing articles of definite length, i.e. discrete articles
- B29C70/46—Shaping or impregnating by compression not applied for producing articles of definite length, i.e. discrete articles using matched moulds, e.g. for deforming sheet moulding compounds [SMC] or prepregs
- B29C70/48—Shaping or impregnating by compression not applied for producing articles of definite length, i.e. discrete articles using matched moulds, e.g. for deforming sheet moulding compounds [SMC] or prepregs and impregnating the reinforcements in the closed mould, e.g. resin transfer moulding [RTM], e.g. by vacuum
-
- 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
- B29C70/00—Shaping composites, i.e. plastics material comprising reinforcements, fillers or preformed parts, e.g. inserts
- B29C70/88—Shaping composites, i.e. plastics material comprising reinforcements, fillers or preformed parts, e.g. inserts characterised primarily by possessing specific properties, e.g. electrically conductive or locally reinforced
- B29C70/887—Shaping composites, i.e. plastics material comprising reinforcements, fillers or preformed parts, e.g. inserts characterised primarily by possessing specific properties, e.g. electrically conductive or locally reinforced locally reinforced, e.g. by fillers
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29D—PRODUCING PARTICULAR ARTICLES FROM PLASTICS OR FROM SUBSTANCES IN A PLASTIC STATE
- B29D99/00—Subject matter not provided for in other groups of this subclass
- B29D99/0032—Producing rolling bodies, e.g. rollers, wheels, pulleys or pinions
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29D—PRODUCING PARTICULAR ARTICLES FROM PLASTICS OR FROM SUBSTANCES IN A PLASTIC STATE
- B29D99/00—Subject matter not provided for in other groups of this subclass
- B29D99/0046—Producing rods
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B60—VEHICLES IN GENERAL
- B60C—VEHICLE TYRES; TYRE INFLATION; TYRE CHANGING; CONNECTING VALVES TO INFLATABLE ELASTIC BODIES IN GENERAL; DEVICES OR ARRANGEMENTS RELATED TO TYRES
- B60C7/00—Non-inflatable or solid tyres
- B60C7/10—Non-inflatable or solid tyres characterised by means for increasing resiliency
- B60C7/101—Tyre casings enclosing a distinct core, e.g. foam
- B60C7/1015—Tyre casings enclosing a distinct core, e.g. foam using foam material
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B60—VEHICLES IN GENERAL
- B60R—VEHICLES, VEHICLE FITTINGS, OR VEHICLE PARTS, NOT OTHERWISE PROVIDED FOR
- B60R19/00—Wheel guards; Radiator guards, e.g. grilles; Obstruction removers; Fittings damping bouncing force in collisions
- B60R19/02—Bumpers, i.e. impact receiving or absorbing members for protecting vehicles or fending off blows from other vehicles or objects
- B60R19/03—Bumpers, i.e. impact receiving or absorbing members for protecting vehicles or fending off blows from other vehicles or objects characterised by material, e.g. composite
-
- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F16—ENGINEERING ELEMENTS AND UNITS; GENERAL MEASURES FOR PRODUCING AND MAINTAINING EFFECTIVE FUNCTIONING OF MACHINES OR INSTALLATIONS; THERMAL INSULATION IN GENERAL
- F16C—SHAFTS; FLEXIBLE SHAFTS; ELEMENTS OR CRANKSHAFT MECHANISMS; ROTARY BODIES OTHER THAN GEARING ELEMENTS; BEARINGS
- F16C3/00—Shafts; Axles; Cranks; Eccentrics
- F16C3/02—Shafts; Axles
- F16C3/026—Shafts made of fibre reinforced resin
-
- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F16—ENGINEERING ELEMENTS AND UNITS; GENERAL MEASURES FOR PRODUCING AND MAINTAINING EFFECTIVE FUNCTIONING OF MACHINES OR INSTALLATIONS; THERMAL INSULATION IN GENERAL
- F16D—COUPLINGS FOR TRANSMITTING ROTATION; CLUTCHES; BRAKES
- F16D3/00—Yielding couplings, i.e. with means permitting movement between the connected parts during the drive
- F16D3/50—Yielding couplings, i.e. with means permitting movement between the connected parts during the drive with the coupling parts connected by one or more intermediate members
- F16D3/72—Yielding couplings, i.e. with means permitting movement between the connected parts during the drive with the coupling parts connected by one or more intermediate members with axially-spaced attachments to the coupling parts
- F16D3/725—Yielding couplings, i.e. with means permitting movement between the connected parts during the drive with the coupling parts connected by one or more intermediate members with axially-spaced attachments to the coupling parts with an intermediate member made of fibre-reinforced resin
-
- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F16—ENGINEERING ELEMENTS AND UNITS; GENERAL MEASURES FOR PRODUCING AND MAINTAINING EFFECTIVE FUNCTIONING OF MACHINES OR INSTALLATIONS; THERMAL INSULATION IN GENERAL
- F16F—SPRINGS; SHOCK-ABSORBERS; MEANS FOR DAMPING VIBRATION
- F16F1/00—Springs
- F16F1/36—Springs made of rubber or other material having high internal friction, e.g. thermoplastic elastomers
- F16F1/366—Springs made of rubber or other material having high internal friction, e.g. thermoplastic elastomers made of fibre-reinforced plastics, i.e. characterised by their special construction from such materials
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29K—INDEXING 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
- B29K2021/00—Use of unspecified rubbers as moulding material
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29K—INDEXING 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
- B29K2101/00—Use of unspecified macromolecular compounds as moulding material
- B29K2101/10—Thermosetting resins
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29L—INDEXING SCHEME ASSOCIATED WITH SUBCLASS B29C, RELATING TO PARTICULAR ARTICLES
- B29L2031/00—Other particular articles
- B29L2031/06—Rods, e.g. connecting rods, rails, stakes
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29L—INDEXING SCHEME ASSOCIATED WITH SUBCLASS B29C, RELATING TO PARTICULAR ARTICLES
- B29L2031/00—Other particular articles
- B29L2031/30—Vehicles, e.g. ships or aircraft, or body parts thereof
- B29L2031/3044—Bumpers
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29L—INDEXING SCHEME ASSOCIATED WITH SUBCLASS B29C, RELATING TO PARTICULAR ARTICLES
- B29L2031/00—Other particular articles
- B29L2031/32—Wheels, pinions, pulleys, castors or rollers, Rims
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29L—INDEXING SCHEME ASSOCIATED WITH SUBCLASS B29C, RELATING TO PARTICULAR ARTICLES
- B29L2031/00—Other particular articles
- B29L2031/32—Wheels, pinions, pulleys, castors or rollers, Rims
- B29L2031/322—Wheels, pinions, pulleys, castors or rollers, Rims made wholly of plastics
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29L—INDEXING SCHEME ASSOCIATED WITH SUBCLASS B29C, RELATING TO PARTICULAR ARTICLES
- B29L2031/00—Other particular articles
- B29L2031/748—Machines or parts thereof not otherwise provided for
- B29L2031/75—Shafts
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29L—INDEXING SCHEME ASSOCIATED WITH SUBCLASS B29C, RELATING TO PARTICULAR ARTICLES
- B29L2031/00—Other particular articles
- B29L2031/774—Springs
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B60—VEHICLES IN GENERAL
- B60R—VEHICLES, VEHICLE FITTINGS, OR VEHICLE PARTS, NOT OTHERWISE PROVIDED FOR
- B60R19/00—Wheel guards; Radiator guards, e.g. grilles; Obstruction removers; Fittings damping bouncing force in collisions
- B60R19/02—Bumpers, i.e. impact receiving or absorbing members for protecting vehicles or fending off blows from other vehicles or objects
- B60R19/18—Bumpers, i.e. impact receiving or absorbing members for protecting vehicles or fending off blows from other vehicles or objects characterised by the cross-section; Means within the bumper to absorb impact
- B60R2019/1806—Structural beams therefor, e.g. shock-absorbing
- B60R2019/1833—Structural beams therefor, e.g. shock-absorbing made of plastic material
- B60R2019/1853—Structural beams therefor, e.g. shock-absorbing made of plastic material of reinforced plastic material
Definitions
- Fibre reinforced plastics composites are conventionally fabricated using epoxide or polyester resins which normally have a low strain to failure of the order of 2-6 per cent for epoxides, and 2-8 per cent for polyesters. Special purpose epoxide and polyester resins are available which can be capable of up to 100 per cent strain and even more, but these are not widely used. Conventional fibre reinforced plastics materials are thus, in the main, limited to applications which do not require great flexibility, or the ability to absorb impacts or tolerate large strains.
- Composites comprising an elastromeric matrix incorporating reinforcing fibres give the designer some increased versatility, in that such a matrix can offer the possibility of much greater strains to failure, and considerably higher capacity for energy absorbency.
- a urethane resin matrix has the potential for elongation of the order of 700%.
- a composite article comprising an elastomeric matrix incorporating reinforcing fibres, and at least one distinct zone of a polymeric stiffening material, said stiffening material being co-polymerised with the elastomeric matrix material within a transition region between the matrix and the stiffening zone.
- the co-polymerisation provides a chemical bond between matrix and stiffening material, and a graded transition from one material to the other. The bond can thus be extremely strong, and the absence of an abrupt transition leads to efficient load transfer with more even stress distribution within the structure of the article. Crack formation and propagation is thus inhibited, and fracture toughness is increased.
- the polymeric stiffening material will itself also incorporate reinforcing fibres. In this case it is then important to arrange for continuity of the fibre reinforcement from matrix to stiffening zone through the transition region. This also contributes greatly to efficient load transfer, even stress distribution etc.
- elastomeric matrix material and polymeric stiffening material can be used, provided that they are mutually compatible, and capable of co-polymerisation.
- co-polymerisation is meant that by an appropriate curing process the matrix and stiffening materials form a chemically cross-linked structure in the transition region, within which molecules of the elastomeric material combine chemically with molecules of the polymeric stiffening material.
- Suitable elastomeric matrix materials include polyurethanes silicone elastomers , natural rubber, polyisopre ⁇ e, styrene butadiene, butadiene, polyacrylics , isobutene isop rene ( butyl rubber) , chloroprene ( neoprene) , nitrile butadiene , chlorosulphonated polyethylene , chlorinated polyethylene , ethylene propylene , flourocarbons , epichlorohydrin, flourosilic ⁇ nes , co-polyesters, styrene co-polymers and olefins.
- Suitable polymeric stiffening materials are normally stiffer than the elastomeric matrix material, and include epoxy resins , polyester resins, phenolic resins , vinyl esters , polyamides , and polyimides.
- One combination which has been found particularly effective is a poly ure thane as the elastomeric matrix material together with an epoxy resin stiffening material.
- Suitable fibres for reinforcement of the elastomer matrix and/ or the polymeric stiffening material are those which are compatible with the respective matrix in which they are incorporated, and include fibres of carbon, boron, glass, nylon, polyester, polyimides, aromatic polyamides (eg Kevlar - Trade Mark), metals and mixtures of fibres of these materials.
- the fibres may be aligned within the elastomer matrix or the stiffening material in one or more preferred directions or planes, so that the article can tolerate enormous elastic linear or shear strains in one or more directions or planes, whilst possessing controlled stiffness as desired in others.
- the invention also resides in numerous articles of specific form in accordance with the invention.
- One such article is an automobile bumper wherein the elastomeric matrix incorporates reinforcing fibres aligned in the plane of the impact face of the bumper, and the polymeric stiffening material is in the form of one or more stiffening strips extending longitudinally within the elastomeric matrix.
- Fixing holes for the bumper should preferably pass through a stiffening strip, and further reinforcement eg in the form of a mass of metal or fibre-reinforced resin is preferably provided around the fixing holes and in contact with the stiffening material.
- Another article which can very advantageously be formed in accordance with the invention is a coupling which is able to transmit torque from a driving member to a driven member, whilst accommodating flexural and/or longitudinal or other movements and possibly misalignment therebetween.
- a very satisfactory design comprises a tubular or cylindrical structure made up of reinforcing fibres inclined symmetrically with respect to the tube or cylinder axis within the elastomeric matrix, and wherein the polymeric stiffening material is provided as a number of longitudinal reinforcing strips parallel to the said axis and within the structure.
- the fibres can be suitably orientated in the elastomeric matrix, for example, by braiding or filament 'winding.
- polymeric stiffening material in the end regions of the structure.
- This can conveniently be in the form of an annulus continuous with or integral with the longitudinal reinforcing strips.
- One such coupling which the invention also makes possible is an automotive constant velocity joint, or a drive shaft replacing two such joints.
- Another very advantegous application for a coupling of this kind is a drive coupling for a helicopter rotor.
- the invention also makes possible an entirely new concept in the form of an integral tyre and wheel,in which the elastomeric matrix forms an outer portion constituting the tyre, and the polymeric stiffening material forms at least part of an inner portion constituting the wheel.
- the reinforcing fibres within the outer portion can be arranged in similar orientations to radial or cross-ply tyres, and might include or consist of conventional reinforcing cords eg of polyester, nylon or steel.
- the polymeric stiffening material may be in the form of a homogeneous material which may contain randomly aligned fibres, or directionally aligned fibures such as layers of square weave or angled ply cloth.
- the polymeric stiffening material may be in the form of radially aligned zones (equivalent to spokes) with other material or voids between the zones. These may contain, for example, radially aligned reinforcing fibres.
- stiffening material in such a design can increase compliance in the rim support so that the wheel rim can act in effect as a spring.
- the integral tyre and wheel offers considerably increased safety as compared with a conventional tubeless tyre/wheel combination.
- the latter can deflate suddenly on impact with an obstacle, because the tyre separates from the wheel rim.
- this is exceeding unlikely to happen, because of the strong chemical bond extending across the transition region between tyre and wheel portions.
- a still further specific article in accordance with the invention is a spring element of zig-zag form (described by the
- Applicant as being of sulcated form), comprising an elongate strip of the elastomeric matrix material incorporating longitudinal zones of polymeric stiffening material, the strip being formed as a zig-zag structure.
- a composite spring comprises a plurality of such zig-zag spring elements.
- a spring assembly may comprise two or more such composite springs, nested one within another.
- Fig 1 is a perspective view of an automobile bumper
- Fig 2 is a sectional perspective view on the line A-A of Fig 1
- Fig 3 is a detailed view of a part of Fig 2, showing the arrangement of a stiffening strip
- Fig 4 is a perspective view of a section of an automobile drive shaft
- Fig 5 shows a insert stiffener for use with the drive shaft of
- Fig 6, 7 and 8 show various ways in which an end fixing can be accomplished
- Fig 9 shows a complete drive shaft assembled in an automobile engine
- Fig 10, 11 and 12 show various possible cross-sections for a helicopter rotor coupling
- Fig 13 shows in section a mould for a helicopter rotor coupling, such as those shown in Figs 10 to 12, Fig 14 and 15 are respectively side and end sectional views of a part of a helicopter rotor coupling,
- Fig 16 is a perspective view of an integral tyre and wheel, partially cut away,
- Fig 17 is a side elevation of a zig-zag spring, partially cut away
- Fig 18 is a plan view of the spring shown in Fig 17, Fig 19 is a perspective view, partially broken away, of a composite spring comprising four spring elements of the kind shown in Figs 17 and 18, and Fig 20 shows a spring assembly comprising two nested spring of the kind shown in Fig 19.
- an automobile bumper 1 comprises a number of layers 2 of continuous long reinforcing fibres in an elastomeric matrix of polyurethane. With the layers 2 of the impact face of the bumper, the continuous reinforcing fibres are aligned in the intended plane of impact, some longitudinally (ie to be horizontal in use) and some inclined at an angle, eg ⁇ 45° or ⁇ 20° to ⁇ 70° to the horizontal.
- the bumper is of generally U-shaped cross-section, and the lay-up of the fibres continued into the limbs of the 'U'.
- the longitudinal fibres provide stiffness to limit distortion to a desirable level on impact of the bumper with a rigid object.
- the inclined fibres also contribute to stiffness, but at the same time provide shear resistance and fracture toughness.
- one, two or more longitudinal stiffening strips 3 which are of a polymeric material such as fibre reinforced epoxy resin or polyester resin, each incorporating longitudinally aligned reinforcing fibres.
- These stiffening strips provide further transverse stiffness where desired, and in particular provide a stiff mounting for reinforcing blocks 4 which are provided with fixing holes for mounting the bumper to a vehicle.
- the reinforcing blocks can also be of fibre-reinforced epoxy resin, and should be assembled in contact with the respective reinforcing strip 3.
- the epoxy resin of the stiffening strip 3 and reinforcing blocks 4 can be cured in situ with the components in their final positions in the bumper, and simultaneously with the curing of the urethane matrix.
- the layers 2 are laid up in a mould as dry fibre layers, with the stiffening strips 3 and reinforcing blocks 4 in position as fibre pre-impregnated with a B-staged epoxy resin.
- Urethane resin together with curing agent is then injected into the mould at a suitable temperature, eg 120-135°C.
- the B-staged epoxy resin is relatively viscous, and remains in position, whilst the urethane resin by virtue of its lower viscosity can easily penetrate the dry layers 2, and surround the strips 3.
- the urethane and epoxy resin materials cure together at the injection temperature, and a transition region Is created between these two materials in which molecular cross-linking occurs between the two resins.
- the fibre reinforced elastomer Tallows the flexibility and high energy absorbency which are highly desirable in an automobile bumper, whilst the fibre reinforced epoxy resin provides added stiffness where needed for impact strength and toughness against front impact, plus a firm anchor for the mounting blocks 4.
- the transition region between the urethane and epoxy resin matrices provides an excellent chemical bond which can tolerate large strains with considerable resistance to debonding.
- Fig 4 there is shown a composite structure suitable for use in an automobile drive joint.
- the structure comprises a plurality of concentric tubular braids 10 of low-angled continuous fibre. The precise angle may be up to ⁇ 60° depending upon the application.
- the continuous fibre can alternatively be filament wound.
- one or more longitudinal stiffening strips 11 (in this instance, four equispaced), each comprising longitudinally aligned and/or angled fibres in an epoxy resin matrix.
- the structure is fabricated by laying up the braids 10 in a mould, together with stiffening strip 11 preimpregnated with a B-staged epoxy resin.
- Urethane resin mixed together with diamine curing agent at 120-135°C is injected into the mould, and the braids are thus thoroughly impregnated on account of the low viscosity of the urethane resin, whilst the epoxy resin is relatively undisturbed.
- Chemical crosslinking between the urethane and epoxy resins occurs in a transition region, as a result of their simultaneous curing in situ.
- a two stage resin injection method can be employed.
- epoxide or another suitable resin system eg polyester
- Urethane resin is then injected so that the areas not penetrated by epoxide are fully impregnated with urethane resin, and the whole is then cured.
- the stiffening strips 11 can be provided as a unitary structure which also includes annular portions 12 at the ends, linking the strips 11.
- the fibres are orientated either longitudinally, or at predetermined positive and negative angles to the longitudinal (eg ⁇ 45° as illustrated) - or in a combination of these orientations.
- the stiffened rings 12 can be employed in various ways, for example as shown in Figs 6, 7 and 8, to facilitate end fixings by means of which torque can be transferred to and from the shaft.
- a metallic end fitting 14 eg of mild steel, can be attached by adhesive bonding.
- the end fitting 14 is of annular form, and the outer layer of braiding 10 is removed so that the annular portion provides a spigot upon which the end fitting 14 is received and s ecured by adhesive bonding.
- the urethaneimpregnated braid deforms to fill the spaces 13 between the stiffening strips 11.
- Fixing holes 15 passing through the end-fitting 14, annular portion 12, and the Inner layer of composite incorporating braid 10, permit attachment to another component.
- Fig 7 shows an alternative arrangement in which the endfittings 14 is provided with a lip 16 , which can be of serrated form.
- the end-fittings 14 is In this case attached by moulding in situ with the remainder of the joint so that the inner braided layer 10, and the annular portion 12 conform to the lip 16.
- Fig 8 shows another arrangement in which the end-fitting 14 is attached by means of mechanical fastenings 17, eg nuts and bolts (as Illustrated) , rivets , etc.
- the end-fittings 14 can alternatively be of fibre reinforced resin such as epoxy resin, and in thise case the resin is advantageously co-cured with the urethane, to provide chemical cross-linking in a transition region.
- Fig 9 shows an automobile engine/ transmission unit 20. On one side of the unit there is shown a conventional drive shaft 21 incorporating a conventional constant velocity joint 22 (one of a pair, the other not shown) . On the other side of the unit, for comparison, the conventional drive shaft and constant velocity joints are all replaced by a drive coupling 23 of construction as described with reference to Fig 4 and 5 and including end f ittings 14 as decribed with reference to any one of Figs 6 to 8.
- the function of the automotive constant velocity joint is to act as a universal joint drive-coupling between the flexibly mounted engine/ transmission unit 20 , and the flexibly mounted road wheels .
- the input velocity must match the output shaft velocity
- the conventional pivoting universal joint must therefore cope with large angular displacements ( ⁇ 22° articulation) since the angle between the wheel axles and the drive shafts changes more than that between the drive shafts and the transmission output shafts.
- a cyclic variation must not occur between the input and output shaft velocities.
- the joint coupling must allow ftfr relative longitudinal movement (by sliding grooves on traditional joints) between the input and output shafts owing to the axle movement, engine mounting (flexibly mounted) movement and chassis flexing movement.
- Torque is transferred to and from the shaft via the end fittings 14 as already described.
- the angled braid 10 provides the torsional stiffness needed for transmitting torque from end to end, whilst the elastomeric nature of the urethane matrix permits considerable transverse flexibility to take up articulation between wheel axles and the transmission output. No cyclic variation in speed is introduced between the two.
- the braided structure in the urethane matrix also provides a substantial degree of longitudinal flexibility so as to accommodate relative longitudinal movements between transmission output and road wheels.
- the longitudinal stiffening strips inhibit "wind-up" due to the applied torque and provide additional torque transmission capability, fracture toughness and impact resistance without unduly inhibiting longitudinal and transverse flexibility.
- FIG. 10 to 12 there are shown various possible crosssections for a helicopter rotor coupling incorporating composite material in accordance with the invention.
- a conventional helicopter main rotor assembly requires a complicated bearing-coupling system to withstand the large shear force components arising from gyroscopic precession and other dynamic rotor changes.
- the present invention makes possible a relatively simple design in which a single composite coupling avoids the need for the conventional complex bearingcoupling system.
- the material for the coupling must have an unusually high ratio of extensional to shear modulus. As shown in Figs 10 to 12, this requirement can be met by a hollow-section coupling comprising tubular braids 30 of continuous fibres (eg carbon fibres) having a low angle of inclination to the longitudinal, the braids being incorporated in a matrix of urethane resin. Longitudinal stiffening strips 31 comprising longitudinally aligned fibres (eg carbon fibres) in an epoxide resin matrix are included between the layers of braid/ urethane. Various configurations of the stiffening zones are possible, as illustrated by way of example in the three figures (Figs 10 to 12) . The urethane and expoxy resins are cured together in situ to provide a chemical bond in a transition region, the bond being highly resistant to delamination.
- the urethane and expoxy resins are cured together in situ to provide a chemical bond in a transition region, the bond being highly resistant to delamination.
- the arrangement shown in Fig 10 enables a good bond to be obtained between urethane and epoxy resin layers , and provides smooth stress distribution through the thickness of the structure.
- the arrangement shown in Fig 11 permits easier fabrication by the insertion of monolithic rib stiffeners 31 , although bonding between layers need to be of a particularly high quality, and stress distribution is less smooth.
- the structure shown in Fig 12 has the advantages of Fig 10, and in addition, the overlapping of layers 31 leads to increased resistance to layer shearing.
- the stiffening zones 31 are made circ ⁇ mf erentially discontinuous in order to permit a degree of flexural movement . Where lower flexural movement is desired, the zones 31 could be made circumf erentially continuous.
- the braided f ibre/urethane structure by virtue of the low fibre angle (normally 1° ⁇ lc 20° ) and elastomeric matrix material Is able to transmit torque to the rotor, but with reduced torsional stiffness so that lagging and torsional motions can be accommodated whilst maintaining manageable control loads.
- the angled braid construction also increases transverse and longitudinal shear toughnes s .
- the strips 31 give increased flexural rigidity ( to withstand precession forces) without significantly increasing tor sional stif fness.
- the . increased rigidity can be controlled by appropriate design of chord length 1. and thickness of the strips t c ( Fig 10) .
- End fixings f or the coupling can be designed along similar lines to those described with reference to Figs 5 to 8 , and the coupling is conveniently fabricated by laying up the dry tubular braids 30 in a mould with the stiffening strips 31 , the latter being impregnated with B-staged epoxy resin. Urethane resin including curing agent is then Injected into the mould at a temperature of about 120-135°C , at which both resin systems cure.
- Figure 13 there is shown a suitable mould for making components of the kind described in relation to Figs 4 to 12.
- the mould casing is constructed in two halves 40 , 41 which split along a parting line 42.
- the casing contains a cylindrical mandrel core 43.
- the upper half 40 of the mould casing is provided along its length with a number of Injection feed holes 45 , and the lower half 41 has likewise a number of outlet ports 46.
- fibre 47 in braided or other f orm is laid up dry on the mandrel 43 and shaped end pieces 44 , longitudinal stiffening strips (not shown) pre-impregnated with epoxy resin being laid up according to design between the dry fibre layers , and end fittings 14 including shaped spigot portions 44 being incorporated according to design.
- Urethane resin with curing agent is injected through ports 46 at a temperature in the range 120° to 135°C.
- the urethane resin owing to its low viscosity readily permeates around the dry fibres and excess urethane resin escapes through ports 46.
- the urethane and expoxy resins both cure rapidly, with a transition region in which the two resins are chemically cross-linked , and the stif fness of the matrix material thus varies progressively. Af ter curing the two mould sections are parted along the line 42, and the core 43 and 44 is removed to leave a finished article , such as a one-piece automotive drive coupling, complete with end f itting.
- Figs 14 and 15 show in greater detail how an end fitting 14 which is especially suitable for connecting between a helicopter rotor blade and the main drive bearing system can be built into the coupling in a mould as described with reference to Fig 13.
- Steel wires 51 are looped through pairs of holes 52 in the fitting, and interleaved with layers of braided fibres 47 and stiffening strips (not shown).
- the end fitting is provided with a spigot 44 having enlarged serrations 55,. by which the end fitting can be firmly located against twisting or longitudinal movements relative to the composite structure.
- the wires 51 looped through the holes 52 provide added security against separation of the end fitting 14 from the remainder of the coupling.
- the coupling After laying the wires 51 in place in the dry condition, the coupling can be finished as previously described in relation to Fig 13.
- a non-symmetrical coupling cross-section such as an aerofoil section, may be more appropriate, as the blade does not rotate about its axis to any great degree.
- Fig 16 illustrates a tyre and wheel of integral construction made possible by use of composite material in accordance with the invention.
- the outer zone 60 constituting the tyre section comprising a urethane matrix incorporating long (continuous) fibres of materials such as carbon, nylon, glass or aromatic polyamide laid up in configurations corresponding to the reinforcing cords in conventional radial or cross-ply tyres. Reinforcing cords of conventional materials such as polyester or steel can also be included in the tyre zone in conventional orientations.
- the tyre tread 61 is moulded in the same urethane material.
- An integral foam core 62 is included during moulding to maintain the tyre in a "inflated" condition.
- the internal volume can be sealed to permit pneumatic Inflation.
- the inner zone 63 of the wheel comprising rim and hub is formed of a fibre-reinforced epoxy resin composite in which the alignment of the fibres Is important for strength and stiffness. Layer combinations of square weave or angled ply cloth, or similar structures derived by machine or hand lay-up would be suitable.
- Fixing holes 64 are provided in the hub area, and fibre reinforced urethane elastomeric matrix material can be included around the fixing holes, cured simultaneously with the expoxy resin. This can lead to reduced stress concentrations as a result of the flexibility, of the urethane, where wheel bolts are tightened.
- the whole assembly is moulded together by laying a pre-preg of the Inner zone 63 in a mould, the pre-preg comprising reinforcing fibres In a B-staged epoxy resin matrix. Dry long fibres are laid according to design around the fixing hole positions and in the tyre z one , and a foam core is introduced.
- the mould i s closed and urethane res in plus diamine curing agent is introduced at a temperature in the range 120-150°C , so that the urethane and expoxy resin materials cure together.
- the urethane resin readily permeates the long fibres in the tyre and fixing hole areas.
- the combined curing creates a transition region in which cross-linking occurs between the two matrix materials, so that stress distribution between the flexible tyre material and the stiff rim, and in the area of the fixing holes , is gradual and smooth.
- the novel structure leads to numerous advantages , including the following :- a. Since there is no tyre/wheel rim interface as is normal with a conventional wheel as sembly , s tress distribution is gradual and smooth , hence there is less chance of catastrophic failure such as an ins tant air loss when tyre and rim are impacted. Also , no damage is transmitted between tyre and rim which is often the case when a metal or plastic wheel rim is accidentally abraded due to tyre fitting or curb impact damage. b.
- a single-element spring 70 of z ig-zag form composed of a matrix of urethane 71 incorporating long (continuous) fibres, and stif fening strips 72 of longitudinally aligned fibres in an epoxy resin matrix. Fixing holes 73 are included at top and bottom.
- the z ig-zag spring differs from the conventional helical spring in that deflections occur as a result of bending rather than torsional deformation of the spring material.
- the long fibres within the urethane matrix are thus aligned so as to resist bending, ie if the spring is imagined as a folded sheet, the fibres are oriented to follow the plane of the sheet.
- these fibres can be laid up by many automated techniques such as braiding, filament winding, tape winding, or woven or knitted cloths can be used.
- the spring is moulded by laying up the stiffening strips as fibres in a B-staged epoxy resin, within a lay-up of the dry continuous fibres.
- Urethane resin plus curing agent in introduced at 120-150° to achieve simultaneous curing of the two resins with a transition zone, as with other embodiments.
- each of four segments 70 has an arcuate lip 74 moulded to its inner edges at top and bottom. These are designed to co-operate with similar lips 74 on other segments so that when fitted together, an annular groove is formed, into which a retaining ring 75 can be snap-fitted at top and bottom to retain the four segments together.
- two ( or possibly more) such complex springs can be nested to achieve performance desired for some applications , eg a non-linear spring rate.
- varying degrees of damping can be incorporated into the spring segments to provide a combined shock absorber/spring system which can cope with varying x-y velocity components.
- the stiffening zones, the thickness, width, angle and length of the limbs can all be designed to obtain large variations in the bending stiffness and torsional stiffness.
- the damping mass of the fibre/elastomeric matrix can be maximised by the increasing number of limbs and their length, thickness and width.
- Large strains are possible due to the use of elastomeric urethane composite, directional stiffness can be 'tailored' by incorporation of co-cured fibre/ epoxy resin strips creating stiff zones, with smooth stress fields in the transition region.
- Non-linear spring rates can be achieved also with the hybrid composite configuration.
- Many fibre fabrication systems can be used in conjunction with resin injection techniques such as braiding, filament winding, tape winding, woven cloth and knitted cloth, on account of the ease of injection moulding with low viscosity urethane. Since the spring's principal mode of operation relies on bending stiffness rather than torsional stiffness which is the principal mode with helical spring construction, the geometrical variables in the zig-zag spring mentioned can be varied to achieve large variations in bending resistance. h.
- a non-linear spring rate characteristic can also be achieved. i. Low weight is possible, j. Low corrosion.
- fibres which are compatible with the matrix concerned and the design requirements.
- Fibres the use of which are within the scope of the invention include carbon, aromatic polyamide such as Kevlar (Trade Mark) , polyimides , glass , and boron.
- epoxy resin Is als o well unders tood in the art to encompass thermosetting resin systems based on polyglycidyl resins which may be cured by homopolymerising (with a catylyst) or co-polymerising (with a hardener) .
- polyglycidyl resins which may be cured by homopolymerising (with a catylyst) or co-polymerising (with a hardener) .
- A Bisphenol
- Epoxidised Novalacs - for good heat resistance Epoxidised Novalacs - for good heat resistance
- epoxy resins can be replaced by other stiffening materials , such as polyester resins , phenolic resins , vinyl es ters , and polyimides in embodiments of the invention, and such a substitution is also considered to be within the scope of the invention.
- the term "urethane” is well understood in the art. In their thermosetting form the urethanes are produced by the reaction of a polyisocyanate with a polyester or polyes ter-bas ed resin. Two general class es of curing agent commonly used are po lyo ls and diamines to give a wide range of physical properties .
- urethane resin includes urethanes which are either homopolymerised or co-polymerised with other suitable materials , for example by the action of a suitable curing agent.
- urethene resins can be replaced in embodiments of the invention by other elastomeric materials , and such a substitution is considered to be within the scope of the invention.
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Abstract
Un article composite comprend une matrice élastomère incorporant des fibres de renforcement, et au moins une zone distincte d'un matériau polymère de raidissement. La matrice élastomère et le matériau polymère sont co-polymérisés à l'intérieur d'une région de transition afin d'obtenir une liaison chimique exceptionnellement forte ainsi qu'une transition graduelle d'un matériau à l'autre. Le matériau de raidissement peut également contenir des fibres de renforcement. Un certain nombre de matériaux possibles sont décrits, ainsi que plusieurs articles de forme spécifique selon l'invention. Les articles décrits sont un pare-choc de voiture (Figures 1-3), des accouplements d'entraînement (Figures 4-8), un joint homocynétique de véhicule automobile (Figure 9), des accouplements de rotor d'hélicoptère (Figures 10-15), un pneu et une roue monobloc (Figure 16) ainsi qu'un ressort en zigzag (Figures 18-20).
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB8316732 | 1983-06-20 | ||
GB838316732A GB8316732D0 (en) | 1983-06-20 | 1983-06-20 | Zone-stiffened composites |
Publications (1)
Publication Number | Publication Date |
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EP0148885A1 true EP0148885A1 (fr) | 1985-07-24 |
Family
ID=10544499
Family Applications (2)
Application Number | Title | Priority Date | Filing Date |
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EP84304110A Withdrawn EP0133340A1 (fr) | 1983-06-20 | 1984-06-18 | Matière composite raidie localement |
EP84902524A Withdrawn EP0148885A1 (fr) | 1983-06-20 | 1984-06-18 | Materiaux composites a zones de raidissement |
Family Applications Before (1)
Application Number | Title | Priority Date | Filing Date |
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EP84304110A Withdrawn EP0133340A1 (fr) | 1983-06-20 | 1984-06-18 | Matière composite raidie localement |
Country Status (4)
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EP (2) | EP0133340A1 (fr) |
JP (1) | JPS60501598A (fr) |
GB (2) | GB8316732D0 (fr) |
WO (1) | WO1985000141A1 (fr) |
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US4812348A (en) * | 1986-06-11 | 1989-03-14 | Volkswagen Ag | Torsion-stressed component part of superposed fiber layers |
US5012028A (en) * | 1986-07-11 | 1991-04-30 | The Standard Oil Company | Process for upgrading light hydrocarbons using oxidative coupling and pyrolysis |
FR2626218B1 (fr) * | 1988-01-27 | 1990-05-25 | Sardou Max | Train de roulement pour vehicule du type automobile |
US5053577A (en) * | 1988-01-15 | 1991-10-01 | The Standard Oil Company | Oxidation catalyst and processes using same |
US4929789A (en) * | 1988-01-15 | 1990-05-29 | The Standard Oil Company | Process for pyrolyzing or thermal cracking a gaseous or vaporized hydrocarbon feedstock using a novel gas-solids contacting device and an oxidation catalyst |
US4836117A (en) * | 1988-01-15 | 1989-06-06 | The Standard Oil Company | Oxidation catalyst and processes using same |
US4968661A (en) * | 1988-01-15 | 1990-11-06 | The Standard Oil Company | Oxidation catalyst amended by examiner |
EP0340818A1 (fr) * | 1988-04-05 | 1989-11-08 | Dsm N.V. | Article moulé à base de polyamide et procédé pour sa fabrication |
GB8822520D0 (en) * | 1988-09-26 | 1988-11-02 | Tech Textiles Ltd | Process for continuously forming reinforced plastics articles |
GB8822521D0 (en) * | 1988-09-26 | 1988-11-02 | Tech Textiles Ltd | Method of producing formable composite material |
FR2645792B1 (fr) * | 1989-04-13 | 1991-10-25 | Aerospatiale | Tube en materiau composite a revetement thermoplastique fibre et procede de fabrication d'un tel tube |
GB8915369D0 (en) * | 1989-07-04 | 1989-08-23 | 3 D Composites | Moulding method |
US5213555A (en) * | 1990-02-27 | 1993-05-25 | Hood Robert L | Exercise equipment information, communication and display system |
FR2661720B1 (fr) * | 1990-05-04 | 1995-04-28 | Hutchinson | Dispositif d'accouplement elastique amorti entre deux parties tournantes coaxiales. |
EP0469364B1 (fr) * | 1990-07-30 | 1996-04-10 | Eaton Corporation | Procédé pour fabriquer et pour la mise sous tension de ressort en matières composites |
MX9206033A (es) * | 1991-10-22 | 1993-05-01 | Univ Brigham Young | Amortiguamiento mejorado en estructuras compuestas a traves de acoplamiento por esfuerzo. |
US5322582A (en) * | 1992-11-27 | 1994-06-21 | Omniglass Ltd. | Pultruded part with localized regions of different resin materials |
US5591104A (en) * | 1993-01-27 | 1997-01-07 | Life Fitness | Physical exercise video system |
FR2749796B1 (fr) * | 1996-06-13 | 1998-07-31 | Plastic Omnium Cie | Procede pour realiser une piece en matiere thermoplastique renforcee, poutre de pare-chocs et pare-chocs comprenant une telle poutre |
WO1998021034A1 (fr) | 1996-11-15 | 1998-05-22 | Brigham Young University | Structures composites amorties presentant des motifs de vagues de fibres et procede et dispositif de fabrication associes |
FR2761434B1 (fr) * | 1997-03-26 | 2000-11-03 | Nantes Ecole Centrale | Dispositif d'absorption d'energie programmable, pour l'attenuation d'un choc |
ATE252989T1 (de) * | 1999-01-25 | 2003-11-15 | Scambia Ind Dev Ag | Anhängevorrichtung und kupplungshaken |
WO2005105417A1 (fr) * | 2004-04-29 | 2005-11-10 | Technische Universität Dresden | Structure creuse realisee en matiere plastique renforcee avec des elements d'introduction de charge |
FR2890591B1 (fr) * | 2005-09-12 | 2012-10-19 | Eads | Procede de fabrication d'une piece composite rtm et piece composite obtenue selon ce procede |
FR2908080B1 (fr) * | 2006-11-06 | 2009-06-26 | Peugeot Citroen Automobiles Sa | Roue gonflage pour vehicule automobile |
DE102007026453A1 (de) * | 2007-06-05 | 2008-12-24 | Technische Universität Dresden | Mehrzellige Verbundstruktur mit Wagenradprofil für Achsen und Wellen |
DE102013221172A1 (de) * | 2013-10-18 | 2015-04-23 | Bayerische Motoren Werke Aktiengesellschaft | Verfahren zum Herstellen eines verstärkten Faserverbundbauteils |
DE102014117571B3 (de) * | 2014-12-01 | 2016-02-18 | Ott-Jakob Spanntechnik Gmbh | Spannvorrichtung |
WO2018125197A1 (fr) * | 2016-12-30 | 2018-07-05 | Compagnie Generale Des Etablissements Michelin | Support structural composite élastique |
JP7223261B2 (ja) * | 2019-02-15 | 2023-02-16 | 三菱ケミカル株式会社 | 自動車用バンパービーム |
JP7178286B2 (ja) * | 2019-02-15 | 2022-11-25 | 三菱ケミカル株式会社 | 自動車用バンパービーム |
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DE1945248A1 (de) * | 1969-01-13 | 1970-07-23 | Fuerstenwalde Reifen Veb K | Verfahren zur haftfesten Bindung von vulkanisierbaren Elastomermischungen an ungesaettigte Polyesterharze |
ZA713222B (en) * | 1970-05-22 | 1972-02-23 | Dunlop Holdings Ltd | Composite structures |
US4076891A (en) * | 1971-11-18 | 1978-02-28 | Dunlop Limited | Product and method of molding plastic-rubber composites |
FR2221930A5 (fr) * | 1973-03-13 | 1974-10-11 | Peugeot & Renault | |
GB1485361A (en) * | 1974-08-05 | 1977-09-08 | Goodwin P | Structures |
GB1511692A (en) * | 1976-02-23 | 1978-05-24 | Secr Defence | Shock absorbing mounts |
FR2513567A1 (fr) * | 1981-09-30 | 1983-04-01 | Peugeot Aciers Et Outillage | Materiau a haute resistance mecanique et thermique a base de polyurethanne et son application a la fabrication de pieces pour vehicules automobiles |
-
1983
- 1983-06-20 GB GB838316732A patent/GB8316732D0/en active Pending
-
1984
- 1984-06-18 GB GB08504111A patent/GB2152429A/en not_active Withdrawn
- 1984-06-18 EP EP84304110A patent/EP0133340A1/fr not_active Withdrawn
- 1984-06-18 WO PCT/GB1984/000214 patent/WO1985000141A1/fr not_active Application Discontinuation
- 1984-06-18 EP EP84902524A patent/EP0148885A1/fr not_active Withdrawn
- 1984-06-18 JP JP59502541A patent/JPS60501598A/ja active Pending
Non-Patent Citations (1)
Title |
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See references of WO8500141A1 * |
Also Published As
Publication number | Publication date |
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GB8504111D0 (en) | 1985-03-20 |
GB2152429A (en) | 1985-08-07 |
WO1985000141A1 (fr) | 1985-01-17 |
JPS60501598A (ja) | 1985-09-26 |
EP0133340A1 (fr) | 1985-02-20 |
GB8316732D0 (en) | 1983-07-20 |
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