Login| Sign Up| Help| Contact|

Patent Searching and Data


Title:
VENEER-BASED PRODUCT AND METHOD OF MANUFACTURE
Document Type and Number:
WIPO Patent Application WO/2002/006042
Kind Code:
A1
Abstract:
A veneer-based product is made of a plurality of veneer layers, a resin biding the layers, and a filler having a high thermal conductivity.

Inventors:
MATUANA LAURENT MALANDA
KING JULIA A
Application Number:
PCT/US2001/022220
Publication Date:
January 24, 2002
Filing Date:
July 13, 2001
Export Citation:
Click for automatic bibliography generation   Help
Assignee:
UNIV MICHIGAN TECH (US)
International Classes:
B27D1/00; B27D1/04; B32B21/08; B32B21/14; (IPC1-7): B32B5/16; B32B18/00; B32B9/04; B32B27/38; B32B27/40; B32B27/00; B32B27/06; B32B23/04; B32B21/04; B05D3/00; B05D5/06; B29C7/02
Foreign References:
US4533589A1985-08-06
US4615936A1986-10-07
Attorney, Agent or Firm:
Gemignani, Joseph A. (WI, US)
Download PDF:
Claims:
CLAIMS We claim :
1. A veneerbased product comprising: a plurality of veneer layers having a thermal conductivity; a resin binding said plurality of veneer layers, the resin having a thermal conductivity; and a filler having a high thermal conductivity mixed with said resin, the thermal conductivity of the filler being greater than the thermal conductivity of the veneer layers and resin.
2. The veneerbased product of claim 1, wherein said filler is selected from the group consisting of carbon fiber, metal coated carbon fiber, carbon nanotubes, natural graphite, coke, synthetic graphite, scrap graphite carbon black, silicon carbide, silicon nitride, boron nitride, metals and mixtures thereof.
3. The veneerbased product of claim 2, wherein the filler is a natural graphite, synthetic graphite or combination thereof.
4. The veneerbased product of claim 1, wherein said filler is about 5% by weight of said resin.
5. The veneerbased product of claim 1, wherein said resin is selected from the group consisting of phenolic resin, urea resin, melamine resin, epoxy resin, urethane resin and mixtures thereof.
6. The veneerbased product of claim 1, wherein said filler is selected from the group consisting of carbon fiber, metal coated carbon fiber, carbon nanotubes, natural graphite, coke, synthetic graphite, carbon black, silicon carbide, silicon nitride, boron nitride, metals and mixtures thereof; said resin is selected from the group consisting of phenolic resin, urea resin, melamine resin, epoxy resin, urethane resin and mixtures thereof; and said filler is about 5% by weight of said resin.
7. The veneerbased product of claim 1 further comprising a wood composite core between the veneer layers.
8. The veneerbased product of claim 1, wherein the thermal conductivity of the filler is greater than. 2 W/mK.
9. The veneerbased product of claim 1, wherein the veneerbased product comprises 4099.5 % by weight veneer layers,. 5050 % by weight resin and. 0550 % by weight filler and further comprises 05 % by weight catalyst.
10. A method for manufacturing veneerbased product comprising: applying an adhesive comprising a resin having a thermal conductivity and a filler having a thermal conductivity to a plurality of veneer layers, the thermal conductivity of the filler being greater than the thermal conductivity of the resin; stacking said plurality of veneer layers with said adhesive; and applying elevated temperature and elevated pressure to said veneer layers to form the veneerbased product.
11. The method of claim 10, wherein said filler is about 5% by weight of said resin.
12. The method of claim 10, wherein said filler is selected from the group consisting of carbon fiber, metal coated carbon fiber, carbon nanotubes, coke, natural graphite, synthetic graphite, scrap graphite carbon black, silicon carbide, silicon nitride, boron nitride, metals and mixtures thereof.
13. The method of claim 10, wherein said resin is selected from the group consisting of phenolic resin, urea resin, melamine resin, epoxy resin, urethane resin and mixtures thereof.
14. The method of claim 10, wherein said filler is selected from the group consisting of carbon fiber, metal coated carbon fiber, carbon nanotubes, coke, natural graphite, synthetic graphite, scrap graphite, carbon black, silicon carbide, silicon nitride, boron nitride, metals and mixtures thereof; said resin is selected from the group consisting of phenolic resin, urea resin, melamine resin, epoxy resin, urethane resin and mixtures thereof; and said filler is about 5% by weight of said resin.
15. The method of claim 10 further comprising incorporating a wood composite core between said veneer layers.
16. The method of claim 10, wherein the thermal conductivity of the filler is greater than. 2 W/mK.
17. The method of claim 1, wherein the veneerbased product comprises 40 99.5 % by weight veneer layers,. 5050 % by weight resin and. 0550 % by weight filler and further comprises 05 % by weight catalyst.
18. A method of reducing press time in the manufacture of a veneerbased product, the method comprising: applying an adhesive comprising a resin having a thermal conductivity and a filler having a thermal conductivity to a plurality of veneer layers, the filler having a thermal conductivity greater than the thermal conductivity of the resin; stacking said plurality of veneer layers with said adhesive; and applying elevated temperature and elevated pressure to said veneer layers to form the veneerbased product.
19. The method of claim 18, wherein the wood composite board comprises 40 99.5 % by weight veneer layers,. 5050 % by weight resin and. 0550 % by weight filler and further comprises 05 % by weight catalyst.
20. The method of claim 19, wherein the filler is a synthetic graphite, natural graphite or combination thereof.
Description:
VENEER-BASED PRODUCT AND METHOD OF MANUFACTURE CROSS-REFERENCE TO RELATED APPLICATIONS This application claims priority under 35 U. S. C. § 119 to provisional patent application no. 60/218,463 filed July 14,2000.

FIELD OF THE INVENTION The present invention relates generally to veneer-based products such as plywood products, laminated veneer lumber (LVL), and parallel strand lumber (PSL). More particularly the present invention relates to the method of manufacture, and products made therefrom, thereof of using a filler having high thermal conductivity, such as metals, carbides, nitrides and carbons in the manufacture of such plywood boards and panels.

BACKGROUND OF THE INVENTION Plywood is a panel product manufactured by gluing together one or more veneers to both sides of a veneer, solid wood, or reconstituted wood core. In the case of solid- wood-core plywood and reconstituted-wood-core plywood, an additional intermediate step is the production of cores, which are made by lateral gluing of blocks or strips of wood or by gluing oriented wood chips or flakes with resin adhesives. Plywood has many advantages over natural wood, an important one being greater dimensional stability. Its uniformity of strength, resistance to splitting, panel form, and decorative value make it adaptable to various uses.

In plywood, both structural and decorative plywood, the grain of alternate layers is typically crossed, in general at right angles ; species, thickness, and grain direction of each layer are matched with those of their opposite number on the other side of the core. The total number of layers of veneers is typically odd (three, five, or more) so that the panel is

balanced around its central axis. This makes plywood stable and less likely to cup, warp, shrink or swell. Thus assembled, the panels are brought to presses, most often hot presses, for gluing with either natural (animal, casein, soybean, starch) or more recently synthetic resins, such as phenol-formaldehyde, urea-formaldehyde, tannin-formaldehyde and urethanes. Certain synthetic resins, such as phenol-formaldehyde, properly used, may produce joints more durable than the natural wood itself-highly resistant to weather, microorganisms, cold, hot and boiling water, and steam and dry heat.

Laminated veneer lumber (LVL) is also produced using the same technology, but unlike plywood, the laminant in LVL are oriented parallel to the longitudinal axis of the panel or beam.

Veneer used for plywood usually varies in thickness from 1/28 to 1/8 inch (0.09 to 0.32 centimeters), but both thinner and thicker veneers often are used. Thin veneers have an advantage, especially for the outer or face plies, in that they set up less severe transverse stresses with changes in moisture content thereby reducing warping and surface checking (superficial cracking) of panels. The use of thin veneer also makes valuable wood go farther. Since successively cut layers of thin veneers are similar in appearance, identical areas from adjacent sheets can be matched to make highly symmetrical ornamental patterns. In lumber-core panels, the plies next to the faces of the crossbands usually are thicker than the face plies and largely control the stability of the panel.

As already mentioned earlier, in a typical veneer-based product manufacturing process, thin sheets of veneer are cross-laminated and glued together with a hot press.

Generally, a resin is used as an adhesive between the plies or veneers which bonded under heat and pressure in a hot press. In addition to high press temperatures, the use of an external catalyst may also accelerate the resin cure rate to shorten the press times. Usually a dilute acid or an acid salt (ammonium sulfate and chloride) in a 20 to 30% solution are

used as external catalysts. Sodium hydroxide, carbonates, and others are also used to promote fast cure of the resins by accelerating the curing of the resin. The external catalyst is generally acceptable only if it will produce shorter press times at lower concentration in the range of 0.25 to 1% by weight of the resin.

Higher pressing temperatures are generally not preferred, at least partly due to higher energy consumption. More importantly, higher press temperatures tend to generate more volatile organic compounds (VOCs) that may adversely affect the environment.

Additional equipment may be needed to prevent the escape of such VOCs. Although press times have been shortened dramatically through these approaches, there is still need to develop cost-effective and environmentally friendly approaches to reduce the press times.

SUMMARY OF THE INVENTION The present invention relates to a plywood comprising a plurality, preferably an odd number, of wood layers, with or without a core ; a resin binding these plurality of wood layers ; and a filler having a high thermal conductivity mixed in with the resin. The resin is preferred to comprise one or more thermoset resin. Examples of preferred resins include, but are not limited to phenolic resins, urea resins, melamine resins, epoxy resins, urethane resins and mixtures thereof.

The present invention also relates to a method for manufacturing plywood comprising: applying an adhesive comprising a resin and a filler having a high thermal conductivity to a plurality of wood layers; stacking the plurality of wood layers with the adhesive ; and applying elevated temperature and elevated pressure to the wood layers to form into the plywood.

BRIEF DESCRIPTION OF THE DRAWINGS Figure 1 is a chart displaying the effects of pressing time on the sheer strength of plywood (3 plies) bonded with phenol-formaldehyde and carbon/phenol-formaldehyde resins.

DETAILED DESCRIPTION OF THE INVENTION In view of the current plywood or panels, products and method thereof, the present invention provides a different plywood board or panels and method of producing such.

The present invention uses an adhesive comprising a resin with a filler having a high thermal conductivity to with resin to bond the plywood veneer or layers. The stacked wood layers are then subjected to hot press at elevated temperature and elevated pressure to produce the plywood product.

Before explaining at least one embodiment of the invention in detail, it is to be understood that the invention is not limited in this application to the details of construction and to the arrangement of the components set forth in the following description. Also, it is to be understood that the phraseology and terminology employed herein are for the purpose of description and should not be regarded as limiting. As such, those skilled in the art will appreciate that the conception, upon which this disclosure is based, may readily be utilized as a basis for the designing of other structures, methods, and systems for carrying out the several purposes of the present invention.

It is an object of the present invention to provide a plywood board or panel product and method thereof which reduces the press time during plywood manufacturing.

These, together with other objects of the invention, along with the various features of novelty which characterize the invention, are pointed out with particularity in the claims annexed to and forming a part of the disclosure. For a better understanding of the

invention, its operating advantages and the specific objects attained by its uses, reference should be made to the accompanying descriptive matter in which there is illustrated preferred embodiments of the invention.

The present invention can be applied to all kinds of veneer-based products including, but not limited to, plywood, plywood product, plywood panels, plywood boards, corrugated plywood products, LVL and PSL. Both structural and decorative plywood products may be produced in accordance with the teachings of the present invention.

A preferred adhesive used herein to bind the various layers, preferred to be an odd number, comprises a filler and a resin. Thermoset resins are preferred resins.

The thermoset resin, which also may be referred to as a binder, includes, but is not limited to, phenolic resin, urea resin (such as urea-formaldehyde), melamine resin, epoxy resin, tannin-formaldehyde, urethane resin and mixtures thereof. A common and preferred phenolic resin is phenol-formaldehyde (PF) resin. Both slow curing and fast curing PF resins may be used. Urethane resins, such as MDI (diphenylmethane diisocyanate) or TDI (toluene diisocyanate) based resins, may be foaming, non-foaming or mixtures thereof.

Non-foaming urethane resins are preferred urethane resins. Foaming urethane resins may be used to impart desired properties either alone or with other thermoset resins disclosed here. A foaming agent may be needed for foaming resins such as foaming urethanes.

Many different materials are suitable for use in the present invention as the"filler." In order to improve heat transfer, a suitable filler should have a thermal conductivity that is higher than the thermal conductivity of the wood pieces or the thermoset resin. Typical thermal conductivity values for some common materials are 0.2 for wood or veneer, 0.2 for resins, 1 for carbon black, 10 for carbonized polyacrylonitrile (PAN) based carbon fibers, 234 for aluminum, 400 for copper, and 600 for graphite (all values in W/mK).

Thus, carbon fillers will act as heat transfer medium by transferring heat from the faces to

the core of the panel quicker. This faster heat transfer will shorten the press time. Carbon is also less hygroscopic than wood ; therefore, carbon improves the dimensional stability, reduce water absorption, reduce linear expansion, and reduce thickness swelling of wood based composites.

Suitable fillers generally have a thermal conductivity greater than the thermal conductivity of the veneer layers and the resins. Suitable fillers having high thermal conductivity include, but are not limited to, a material selected from the group consisting of carbon filler, carbides, nitrides, metals, conducting polymers and mixtures thereof. A carbon filler may be selected from carbon fiber, metal (such as nickel) coated carbon fiber, carbon nanotubes, natural graphite, synthetic graphite (including high purity synthetic graphite), scrap graphite, various forms of coke, carbon black, and mixtures thereof.

Carbides may be selected from the group consisting of silicon carbide, tungsten carbide, and mixtures thereof. Non-limiting examples of nitrides include boron nitride, various forms of silicon nitride and mixtures thereof. Suitable metals include, but are not limited to, aluminum, zinc, tungsten, iron, copper, titanium, tin, metal alloys and mixtures thereof.

Many different types of known conducting polymers also may be used as the filler for the present invention. Non-limiting examples include doped or non-doped polyaniline, polypyrrole, and mixtures thereof.

The adhesive may further comprise an situ or ex-situ"catalyst."A catalyst here means a small amount of a material which can be used to increase curing of the thermoset resin, increase forming of the board or panel under the conditions, or both. Accordingly, any catalyst that is known to accelerate curing of any type of the thermoset resins disclosed herein is included, such as acid, base, etc. It should be understood that not every catalyst will work for all of the disclosed thermoset resins.

The overall plywood has a general composition, by weight percent, as follows:

wood layers, 40 to 99.9; resin, 0.1 to 50; filler, 0.05 to 50 ; catalyst, 0 to 5. It is preferred that the weight of the filler is about 5% of the weight of the resin.

In a accordance with an exemplary embodiment of the invention, a plywood board or panel, such as but not limited to 3 ply construction, is formed with the addition of a carbon filler. A preferred embodiment being carbon fibers, such as but not limited to carbon fibers available from Conoco, Inc. with the trademark THERMOCARB@.

THERMOCARBs is a high purity synthetic graphite, which has the general properties as listed in Table 1 below.

Table 1 Ash <0. 1 wt% Sulfur 0. 02 wt% Vibrated Bulk Density 0. 66 g/cc Density 2. 24 g/cc Particle Sizing, vol% (by Sieve Method) +48Tyler Mesh* 4 -48/+80 Tyler Mesh 22 -80/+200Tyler Mesh 48 -200/+325TylerMesh 16 -325TylerMesh 10 Thermal Conductivity at 23C 600. W/mK on a 1/4"particle Electrical Resistivity 10-4 ohm-cm (approximate) Particle Aspect Ratio 2. 0 Particle Shape Irregular "-4S iyler Mesh = 297 Microns 80 Tyler Mesh = 177 Microns 200 Tyler Mesh = 74 Microns 325 Tyler Mesh = 44 Microns It will be understood that various types of graphite or various types of carbon may be utilized with the scope of the invention.

According to the invention, carbon is added to a thermoset resin, such as liquid phenol formaldehyde (PF) resin to form a satisfactory glue bond during the manufacture of plywood products. The liquid PF resin used was GP 3121 ResiStran from Georgia-Pacific.

Table 2 lists the properties of this resin.

Table 2 pH approx. 10 Specific Gravity @ 25°C, g/cc 1. 22 Wt% Volatile Matter 46.

Veneers, such as but not limited to Aspen (5 wt% moisture content), are bonded using pure liquid PF (as a control) and a mixture of PF synthetic graphite adhesive. The concentration of synthetic graphite in the adhesive mixture was fixed at 5% by weight of total amount of the resin. Plywood was generally formed as follows: first, 60 g/m2 per single glue line of the adhesive was spread on the surface of the veneers. Second, three veneers were laid up together with the grain direction of adjacent veneers perpendicular to one another (0°/90°/0°) to form a mat. Finally, the formed mat was hot pressed at 320°F (160°C) using 250 psi (1725 kPa) pressure. The press closing time to full pressure was 15 seconds and the assembly times for resin curing were 1,1.5 and 2 minutes.

The glueline performance of the manufactured product was measured using plywood shear specimens according to the procedure outlined in ASTM D906, Standard Test Method for Strength Properties of Adhesives in Plywood Type Construction in Shear by Tension Loading, to determine the failure load and percentage of wood failure.

The shear strength results in pounds per square inch (glue line performance, mean and standard deviation) are summarized in Table 3. For each material and each press time, 10 tests were conducted. These results are illustrated in Figure 1, with 95% confidence intervals illustrated as brackets.

Table 3 Composites Shear stress (psi) 1 min 1. 5 min 2 min PF Resin Only Used 334 50 370 24 434 18 PF + 5% THERMOCARB 280 : L 66 343 47 411 20

Figure 1 shows that the 95% confidence intervals overlap for all 3 pressing times for the control plywood and the plywood containing synthetic graphite.

Table 4 lists the percentage of wood failures (versus resin failure) in these samples.

The results show that a press time of 1 minute did not allow sufficient time for the resin to cure. The control and the plywood containing synthetic graphite both demonstrated resin layer interface failures. For the 1.5 minute press time, the synthetic graphite containing plywood exhibited improved adhesion as indicated by the higher percentage of wood failure (versus resin failure). For the 2 minute press time, the opposite was observed.

Table 4 shows the effects of pressing time on the percentage of wood failure of plywood (3 plies) bonded with phenol-formaldehyde and phenol-formaldehyde resins.

Table 4 Composites Percentage of wood failure Imin1.5 min 2 min Pure PF resin 0 0-5 100 PF + 5% Synthetic Graphite 0 15 70

The present invention has been described in relation to the drawings and examples attached hereto. They are intended for illustration purposes only. It should be understood that other and further modifications, apart from those shown or suggested herein, may be made within the spirit and scope of this invention, which is defined by the above written description and the claims below.