GB2161424A - Energy absorbant laminates - Google Patents
Energy absorbant laminates Download PDFInfo
- Publication number
- GB2161424A GB2161424A GB08516562A GB8516562A GB2161424A GB 2161424 A GB2161424 A GB 2161424A GB 08516562 A GB08516562 A GB 08516562A GB 8516562 A GB8516562 A GB 8516562A GB 2161424 A GB2161424 A GB 2161424A
- Authority
- GB
- United Kingdom
- Prior art keywords
- laminate
- laminae
- polymeric elastomer
- energy
- elastomer adhesive
- 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
Links
Classifications
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B21/00—Layered products comprising a layer of wood, e.g. wood board, veneer, wood particle board
- B32B21/13—Layered products comprising a layer of wood, e.g. wood board, veneer, wood particle board all layers being exclusively wood
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B21/00—Layered products comprising a layer of wood, e.g. wood board, veneer, wood particle board
- B32B21/14—Layered products comprising a layer of wood, e.g. wood board, veneer, wood particle board comprising wood board or veneer
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B15/00—Layered products comprising a layer of metal
- B32B15/02—Layer formed of wires, e.g. mesh
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B7/00—Layered products characterised by the relation between layers; Layered products characterised by the relative orientation of features between layers, or by the relative values of a measurable parameter between layers, i.e. products comprising layers having different physical, chemical or physicochemical properties; Layered products characterised by the interconnection of layers
- B32B7/04—Interconnection of layers
- B32B7/12—Interconnection of layers using interposed adhesives or interposed materials with bonding properties
-
- 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
- F16F1/3605—Springs made of rubber or other material having high internal friction, e.g. thermoplastic elastomers characterised by their material
-
- 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
- F16F9/00—Springs, vibration-dampers, shock-absorbers, or similarly-constructed movement-dampers using a fluid or the equivalent as damping medium
- F16F9/30—Springs, vibration-dampers, shock-absorbers, or similarly-constructed movement-dampers using a fluid or the equivalent as damping medium with solid or semi-solid material, e.g. pasty masses, as damping medium
- F16F9/306—Springs, vibration-dampers, shock-absorbers, or similarly-constructed movement-dampers using a fluid or the equivalent as damping medium with solid or semi-solid material, e.g. pasty masses, as damping medium of the constrained layer type, i.e. comprising one or more constrained viscoelastic layers
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B2260/00—Layered product comprising an impregnated, embedded, or bonded layer wherein the layer comprises an impregnation, embedding, or binder material
- B32B2260/02—Composition of the impregnated, bonded or embedded layer
- B32B2260/026—Wood layer
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B2260/00—Layered product comprising an impregnated, embedded, or bonded layer wherein the layer comprises an impregnation, embedding, or binder material
- B32B2260/04—Impregnation, embedding, or binder material
- B32B2260/046—Synthetic resin
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B2307/00—Properties of the layers or laminate
- B32B2307/10—Properties of the layers or laminate having particular acoustical properties
Landscapes
- Engineering & Computer Science (AREA)
- General Engineering & Computer Science (AREA)
- Life Sciences & Earth Sciences (AREA)
- Wood Science & Technology (AREA)
- Mechanical Engineering (AREA)
- Laminated Bodies (AREA)
Abstract
Laminate materials are produced from at least two layers of wood veneer and are bonded by and impregnated with a polymeric elastomer adhesive under conditions of heat and pressure. Laminates so produced exhibit energy absorbing, vibration damping properties together with visco elastic behaviour.
Description
SPECIFICATION
Energy absorbant laminates
This invention relates to the field of laminate materials incorporating wood veneer layers.
Laminates constructed of wood Iaminae bonded with thermosetting resins, eg phenolic resins, are well known for example as plywood. Hitherto wood laminates have been produced with strength and rigidity in mind for construction and cladding applications. In contrast, the laminates to which this invention relates exhibit energy absorbant properties in that they are readily deformed in directions across the plane of the laminate and are slow to recover the original configuration when a deforming stress is removed. These are not qualities associated with prior art wooden laminates nor are they desirable qualities in the usual applications for which plywood are intended. Moreover the laminates of the invention are resistant to impact shattering and delamination.Hard impacts exceeding the elastic limits can be absorbed by materials of the invention with only localised indentation damage. It is anticipated that the materials of the invention will find applications in shock and vibration absorbant applications and applications requiring resistance to vandal damage.
Accordingly the invention comprises an energy absorbant laminate comprising at least two laminae of wood veneer each impregnated with, and bonded within the laminate by, a polymeric elastomer adhesive. The term "wood veneer" is intended to cover only natural wood not reconstituted wood nor artificial veneers, and only wood in thicknesses up to approximately 2 mm. The polymeric elastomer adhesive may be based on a natural or a synthetic rubber but it must have sufficient adhesive qualities to bond the laminate together. An attempt to produce satisfactory laminates using unvulcanised rubber in solution was not successful as the laminate became delaminated when flexed.
The number of laminae within the laminate will depend upon the required properties of the material. Moreover the degreeof impregnation of the wood veneer laminae may be varied between a minimal surface impregnation sufficient only to bond the layers, to a much greater degree and depth of impregnation which produces a more flexible'and impact resistant laminate. The grain orientation of the wood veneer laminae within the laminate can be arranged to either an aligned or a distributed pattern so as to respectively enhance or reduce anisotropic properties.
The laminate of the invention may be reinforced by the inclusion of a layer or layers synthetic fibres such as carbon, boron or aramid fibres (aramid is a trade mark) and these can be woven or unwoven, continuous or discontinuous. In laminates so reinforced not all wood veneer layers will be bonded directly to another such layer. Indeed the laminate of the invention may be predominantly based on a fibre-reinforced composite having a number (at least two) of elastomer-impregnated and bonded wood veneer layers as replacement for synthetic fibre layers which might reduce the cost of the laminate and confer enhanced energy absorbant properties.
Furthermore, the.laminate of the invention can include metal wires or foils for either electrical purposes (such as screening) or for reinforcement.
The invention also provides a method for the production of an energy absorbant laminate including at least two laminae of wood veneer, the method comprising impregnating laminae and bonding them together to a desired laminar configuration, with a polymeric elastomer adhesive under conditions of heat and pressure. The Iaminae may be impregnated, and subsequently bonded, with adhesive applied to individual laminae from solution. In this case the impregnation will preceed the layup of the laminae and subsequent bonding.
Alternatively the adhesive may be in the form of thin film material and in this case the impregnation and bonding is likely to be combined as a single step. The degree of impregnation can be increased by impregnating individual wood veneers under pressure prior to lay up. This is principally, but not necessarily solely, applicable to impregnation using adhesives in solution.
The method of the invention may also include a further feature, that of heating the wood Iaminae in a liquid solvent prior to impregnation in order to modify the grain structure of the wood and render it more receptive to subsequent impregnation. For the purposes of this feature water should be considered as a solvent, and glycerol is another suitable liquid. If glycerol is used then there could be advantage in leaving some of the glycerol within the wood structure at the impregnation stage in order to render the wood veneers more flexible. Otherwise the solvent will be extracted from the wood veneers (together with the dissolved constituents of the wood) by evacuation or evaporation prior to impregnation.
Materials of the invention have been produced from veneers of beech, walnut, crown oak, and both striped and crown mahogany. Different woods cbnfir differing combinations of properties and costs. Beech for example is difficult to impregnate with polymeric elastomer adhesive and results in a stiffer less damped material whilst striped mahogany is easy to impregnate and results in a more damped and impact tolerant material.
Where thin films of thermoplastic elastomer adhesives are used the principal method of wood impregnation- and bonding is to heat the stacked laminations and interleaved films to a temperature of about 210 degrees Celcius and to press at temperatures at a pressure of approximately 20 Ib/in2
Coating of the wood veneer with elastomerie adhesive solutions may be by brushing, spraying or immersion. Coated wood veneer laminations may be left to dry before being impregnated and bonded.
In order that the present invention may be more fully understood examples will now be given by way of illustration only.
Example 1
Crown mahogany veneer, 0.5 mm thick, was brush coated on each side with Dunlop S758 (trade mark), a solvent-based tubbery adhesive. Pieces of the coated veneer were placed individually (between sheets of release film) on a vacuum table and pressed at atmospheric pressure for 5 minutes to effect an initial impregnation of the wood. These pieces were then removed from the vacuum table and dried for a further 5 minutes in an oven at 60"C. Three pieces of the veneer so treated were then stacked on top of each other with the grain directions at right angles and were pressed at a pressure of 500 Ib/in2 at room temperature.
The resulting material had a high degree of flexibility and toughness. When bent the material did not spring back to its original shape on release but slowly resumed its original shape exhibiting visco elastic properties.
Example 2
Crown mahogany veneer was again used with
Dunlop S758 (trade mark) adhesive but this time the adhesive was diluted with trichloroethane in a
ratio of approximately 2:1 (solvent:adhesive). The veneer was given four brush coats on each face, drying in an oven at 600C for five minutes between each coat. A final coat of undiluted adhesive was given and dried to a tack-free state. Three pieces of coated veneer were then stacked together and
pressed at a pressure of 500 ib/in2 at room temperature.
The laminate thus produced again exhibited a
high degree of toughness and flexibility with pro
nounced vibration damping qualities and the viscoelastic characteristics mentioned in Example 1.
Example 3
Crown mahogany veneer was again treated in a
similar fashion to Example 1 but in-this case ten
laminations of veneer were stacked and pressed.
The laminate so produced though more rigid than the materials of Examples 1 and 2, again exhibited
visco elastic properties.
It was very noticeable that all-the materials pro
duced were not springy but exhibited energy ab
sorbing, vibration damping properties
In the examples given above densities of the ma
terials produced were measured. In all cases the
measured density was approximately 0.8 gm/ml, a
low density compared to plastics materials.
The method of Example 2 appeared to give better impregnation of the wood veneer due partly to the lower viscosity of the diluted adhesive.
Example 4
Laminates were made from striped and crown
mahogany, beech and teak veneers (all approxi
mately 0.6 mm in thickness) with a thermoplastic
polyester elastomer adhesive. The adhesive used
was Du Pont Hytrel (trade name) in type-designa
tions 4055, 5526, 6346 and 7246 l listed in order of
increasing stiffness. Both 3 and 5 ply laminates
were produced with the grain directions staggered
at right angles between layers.
One partricular laminate of this kind is descri.bed below in more detail to illustrate the method of
preparation and the properties exhibited. This Lam- inate was made from five pieces of striped mahog
any veneer 0.6 mm thick and cut to an overall size
of 10 cm x 6 cm with the grain parallel to the
longer edge in 3 pieces and with the grain parallel to the shorter edge in the others. Hytrel (trade
name) 4055 adhesive, received in the form of grain ules was made into a film of about 0.3 mm thick
ness by pressing the granules between the plates
of a press at about 210 degrees Celcius. Four
pieces of the film were cut, each to dimensions of
11 cm x 7 cm and interleaved between the cut
wood veneers.The veneers were stacked so that
the central and outermost layers were the ones
having grain direction parallel to their longer
edges. The assembly of stacked veneers and adhe
sive films was pressed under pressure of approxi
mately 20 Ib/in2 at about 210 degrees Celcius for 30
seconds, removed from the hot press and cooled
under a similar pressure I to prevent warpage. The flexural modulus of this laminate, when flexed as a
beam across the grain of the surface veneers, was
790 KN/cm2.
All the laminates produced, of this kind, exhibit a
degree of energy absorbance but this is less pro
nounced than in laminates produced from solvent
based adhesives, because the adhesive does not
impregnate the veneers to a similar extent. More
over the laminates exhibited flexure and toughness
dependent I all other parameters being equal I on
the grade of adhesive utilised.
The examples described in this specification
have been of simple flat laminates, however the in
vention is not restricted in application to flat prod
ucts. As will be apparent to one of ordinary skill in
the art, a significant degree of curvature may be
introduced at the lamination stage by conventional
wood processing techniques. Laminates made with
thermoplastic adhesives may also be susceptable
to post-lamination forming by hot pressing. In re
gard to laminates made from thermoplastic adhe-- sive, care needs to be exercised with regard to
selection of a suitable laminating temperature and
a suitable lamination thickness. Otherwise the tem erature gradient established by hot press laminat
ing, between the outside and interior of the
laminate might result in either insufficient melting
of adhesive in the interior region or charring of the
outermost veneers.
Claims (10)
1. An energy absorbant laminate comprising at
least two laminae of wood veneer each impreg
nated with and bonded within the laminate by, a
polymeric elastomer adhesive.
2. An energy absorbant laminate as claimed in
Claim 1 including at least one lamina of synethic
fibre reinforcement material.
3. An energy absorbant laminate as claimed in
Claim 1 or Claim 2 including a metal wire or wires
or a metal foil.
4. A method for production of an energy ab sorbant laminate including at least two Iaminae of wood veneer, the method comprising impregnating and bonding together to a desired laminar configuration, laminae with a polymeric elastomer adhesive under conditions of heat and pressure.
5. A method as claimed in Claim 4 wherein the polymeric elastomer adhesive is applied to laminae from a solvent solution prior to lay up of the laminae.
6. A method as claimed in Claim 4 wherein the polymeric elastomer adhesive is applied to the laminae in film form.
7. A method as claimed in any one of claims 46 in which at least one of the wood veneer Iaminae is impregnated with the polymeric elastomer adhesive under pressure, prior to inclusion in the lay-up of the laminae.
8. A method as claimed in any one of Claims 47 in which at least one wood veneer lamina is heated under liquid solvent prior to impregnation with the polymeric elastomer adhesive.
9. An energy absorbant laminate as claimed in
Claim 1 and substantially as hereinbefore described with reference to the foregoing examples.
10. A method for production of an energy absorbant laminate as claimed in Claim 4 and substantially as hereinbefore described with reference to the foregoing examples.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB848417704A GB8417704D0 (en) | 1984-07-11 | 1984-07-11 | Laminate materials |
Publications (3)
Publication Number | Publication Date |
---|---|
GB8516562D0 GB8516562D0 (en) | 1985-08-07 |
GB2161424A true GB2161424A (en) | 1986-01-15 |
GB2161424B GB2161424B (en) | 1988-02-03 |
Family
ID=10563744
Family Applications (2)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB848417704A Pending GB8417704D0 (en) | 1984-07-11 | 1984-07-11 | Laminate materials |
GB08516562A Expired GB2161424B (en) | 1984-07-11 | 1985-07-01 | Energy absorbant laminates |
Family Applications Before (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB848417704A Pending GB8417704D0 (en) | 1984-07-11 | 1984-07-11 | Laminate materials |
Country Status (1)
Country | Link |
---|---|
GB (2) | GB8417704D0 (en) |
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0384899A1 (en) * | 1989-02-22 | 1990-08-29 | IVECO FIAT S.p.A. | A leaf spring of composite material for vehicle suspensions and a method for its manufacture |
FR2702700A1 (en) * | 1993-03-15 | 1994-09-23 | Rhein Philippe | Flexible and pliable multi-ply structure |
US20160311194A1 (en) * | 2015-04-23 | 2016-10-27 | Goodrich Corporation | Flexible veneer panel with metal mesh layer |
SE1751254A1 (en) * | 2017-10-10 | 2019-04-11 | Manick Intellectual Property Ab | Method and apparatus for manufacturing wooden products |
Citations (11)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB1088136A (en) * | 1965-06-14 | 1967-10-25 | Border Chemical Company Uk Ltd | Improvements in or relating to flush doors and a process for the manufacture of same |
GB1099187A (en) * | 1964-06-04 | 1968-01-17 | Koppers Co Inc | A method of making phenol-resorcinol-formaldehyde resins |
GB1172682A (en) * | 1966-03-04 | 1969-12-03 | Aaronson Bros Ltd | Improvements in or relating to Wood Veneer. |
GB1305288A (en) * | 1970-05-29 | 1973-01-31 | ||
GB1458529A (en) * | 1973-03-27 | 1976-12-15 | Sumitomo Bakelite Co | Method of bonding wet wood with an adhesive composition |
GB1469276A (en) * | 1973-09-17 | 1977-04-06 | Sadashige Fancy Plywood Ind Co | Process for producing sliced veneer |
GB1472629A (en) * | 1973-09-29 | 1977-05-04 | Marukei Mokko Kk | Process for manufacturing a decorative panel impressed with a permanent embossed pattern |
GB1493938A (en) * | 1965-10-22 | 1977-11-30 | Aaronson Bros Ltd | Method of manufacturing fabricated wood veneers |
GB1504451A (en) * | 1974-03-13 | 1978-03-22 | Keskuslaboratorio | Adhesives |
GB1517505A (en) * | 1974-08-28 | 1978-07-12 | Wynn Ltd G | Sectional members |
GB1568285A (en) * | 1976-11-19 | 1980-05-29 | Dehn Holding As | Method of manufacturing surface treated boards from wood veneer or chips |
-
1984
- 1984-07-11 GB GB848417704A patent/GB8417704D0/en active Pending
-
1985
- 1985-07-01 GB GB08516562A patent/GB2161424B/en not_active Expired
Patent Citations (11)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB1099187A (en) * | 1964-06-04 | 1968-01-17 | Koppers Co Inc | A method of making phenol-resorcinol-formaldehyde resins |
GB1088136A (en) * | 1965-06-14 | 1967-10-25 | Border Chemical Company Uk Ltd | Improvements in or relating to flush doors and a process for the manufacture of same |
GB1493938A (en) * | 1965-10-22 | 1977-11-30 | Aaronson Bros Ltd | Method of manufacturing fabricated wood veneers |
GB1172682A (en) * | 1966-03-04 | 1969-12-03 | Aaronson Bros Ltd | Improvements in or relating to Wood Veneer. |
GB1305288A (en) * | 1970-05-29 | 1973-01-31 | ||
GB1458529A (en) * | 1973-03-27 | 1976-12-15 | Sumitomo Bakelite Co | Method of bonding wet wood with an adhesive composition |
GB1469276A (en) * | 1973-09-17 | 1977-04-06 | Sadashige Fancy Plywood Ind Co | Process for producing sliced veneer |
GB1472629A (en) * | 1973-09-29 | 1977-05-04 | Marukei Mokko Kk | Process for manufacturing a decorative panel impressed with a permanent embossed pattern |
GB1504451A (en) * | 1974-03-13 | 1978-03-22 | Keskuslaboratorio | Adhesives |
GB1517505A (en) * | 1974-08-28 | 1978-07-12 | Wynn Ltd G | Sectional members |
GB1568285A (en) * | 1976-11-19 | 1980-05-29 | Dehn Holding As | Method of manufacturing surface treated boards from wood veneer or chips |
Cited By (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0384899A1 (en) * | 1989-02-22 | 1990-08-29 | IVECO FIAT S.p.A. | A leaf spring of composite material for vehicle suspensions and a method for its manufacture |
FR2702700A1 (en) * | 1993-03-15 | 1994-09-23 | Rhein Philippe | Flexible and pliable multi-ply structure |
US20160311194A1 (en) * | 2015-04-23 | 2016-10-27 | Goodrich Corporation | Flexible veneer panel with metal mesh layer |
US10814582B2 (en) * | 2015-04-23 | 2020-10-27 | Goodrich Corporation | Flexible veneer panel with metal mesh layer |
SE1751254A1 (en) * | 2017-10-10 | 2019-04-11 | Manick Intellectual Property Ab | Method and apparatus for manufacturing wooden products |
WO2019074434A1 (en) * | 2017-10-10 | 2019-04-18 | Manick Intellectual Property Ab | Method and apparatus for manufacturing wooden products |
Also Published As
Publication number | Publication date |
---|---|
GB2161424B (en) | 1988-02-03 |
GB8417704D0 (en) | 1984-08-15 |
GB8516562D0 (en) | 1985-08-07 |
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Legal Events
Date | Code | Title | Description |
---|---|---|---|
732 | Registration of transactions, instruments or events in the register (sect. 32/1977) | ||
732E | Amendments to the register in respect of changes of name or changes affecting rights (sect. 32/1977) | ||
PCNP | Patent ceased through non-payment of renewal fee |
Effective date: 20030701 |