US2068759A - Method of making plywood - Google Patents
Method of making plywood Download PDFInfo
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- US2068759A US2068759A US35884A US3588435A US2068759A US 2068759 A US2068759 A US 2068759A US 35884 A US35884 A US 35884A US 3588435 A US3588435 A US 3588435A US 2068759 A US2068759 A US 2068759A
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- Prior art keywords
- core
- moisture content
- coating
- plywood
- binder
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- 239000011120 plywood Substances 0.000 title description 19
- 238000004519 manufacturing process Methods 0.000 title description 10
- 238000000576 coating method Methods 0.000 description 28
- 239000011230 binding agent Substances 0.000 description 25
- 239000011248 coating agent Substances 0.000 description 25
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 24
- 239000000243 solution Substances 0.000 description 18
- 239000000463 material Substances 0.000 description 16
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 15
- 239000007859 condensation product Substances 0.000 description 12
- 238000001035 drying Methods 0.000 description 11
- 239000000203 mixture Substances 0.000 description 10
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 9
- 239000007864 aqueous solution Substances 0.000 description 8
- 235000011121 sodium hydroxide Nutrition 0.000 description 8
- QTWJRLJHJPIABL-UHFFFAOYSA-N 2-methylphenol;3-methylphenol;4-methylphenol Chemical compound CC1=CC=C(O)C=C1.CC1=CC=CC(O)=C1.CC1=CC=CC=C1O QTWJRLJHJPIABL-UHFFFAOYSA-N 0.000 description 7
- 239000002023 wood Substances 0.000 description 7
- 244000068988 Glycine max Species 0.000 description 6
- 235000010469 Glycine max Nutrition 0.000 description 6
- 238000006243 chemical reaction Methods 0.000 description 6
- 239000004615 ingredient Substances 0.000 description 6
- 235000013312 flour Nutrition 0.000 description 5
- 238000000034 method Methods 0.000 description 5
- 229920005989 resin Polymers 0.000 description 5
- 239000011347 resin Substances 0.000 description 5
- GSEJCLTVZPLZKY-UHFFFAOYSA-N Triethanolamine Chemical compound OCCN(CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-N 0.000 description 4
- 239000006185 dispersion Substances 0.000 description 4
- 238000007731 hot pressing Methods 0.000 description 4
- 238000003825 pressing Methods 0.000 description 4
- 238000003756 stirring Methods 0.000 description 4
- 238000010276 construction Methods 0.000 description 3
- 238000004880 explosion Methods 0.000 description 3
- 125000002485 formyl group Chemical class [H]C(*)=O 0.000 description 3
- 238000001556 precipitation Methods 0.000 description 3
- 229920003002 synthetic resin Polymers 0.000 description 3
- 239000000057 synthetic resin Substances 0.000 description 3
- 235000017060 Arachis glabrata Nutrition 0.000 description 2
- 244000105624 Arachis hypogaea Species 0.000 description 2
- 235000010777 Arachis hypogaea Nutrition 0.000 description 2
- 235000018262 Arachis monticola Nutrition 0.000 description 2
- 108010082495 Dietary Plant Proteins Proteins 0.000 description 2
- 239000000470 constituent Substances 0.000 description 2
- 235000020232 peanut Nutrition 0.000 description 2
- 239000007921 spray Substances 0.000 description 2
- 238000003892 spreading Methods 0.000 description 2
- 235000013311 vegetables Nutrition 0.000 description 2
- HZAXFHJVJLSVMW-UHFFFAOYSA-N 2-Aminoethan-1-ol Chemical compound NCCO HZAXFHJVJLSVMW-UHFFFAOYSA-N 0.000 description 1
- -1 36 parts Chemical compound 0.000 description 1
- 241000196324 Embryophyta Species 0.000 description 1
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
- 244000046052 Phaseolus vulgaris Species 0.000 description 1
- 235000010627 Phaseolus vulgaris Nutrition 0.000 description 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 239000004202 carbamide Substances 0.000 description 1
- 150000001720 carbohydrates Chemical class 0.000 description 1
- 235000014633 carbohydrates Nutrition 0.000 description 1
- 210000002421 cell wall Anatomy 0.000 description 1
- 239000001913 cellulose Substances 0.000 description 1
- 229920002678 cellulose Polymers 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 229940051043 cresylate Drugs 0.000 description 1
- 230000007547 defect Effects 0.000 description 1
- 238000007865 diluting Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 239000003995 emulsifying agent Substances 0.000 description 1
- 239000000839 emulsion Substances 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- 239000012467 final product Substances 0.000 description 1
- 239000003292 glue Substances 0.000 description 1
- 230000005484 gravity Effects 0.000 description 1
- 239000012535 impurity Substances 0.000 description 1
- 238000010030 laminating Methods 0.000 description 1
- 238000003475 lamination Methods 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 230000035515 penetration Effects 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 229920000136 polysorbate Polymers 0.000 description 1
- 239000011148 porous material Substances 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- 108090000623 proteins and genes Proteins 0.000 description 1
- 102000004169 proteins and genes Human genes 0.000 description 1
- 239000011541 reaction mixture Substances 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 239000006228 supernatant Substances 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
- C09J161/00—Adhesives based on condensation polymers of aldehydes or ketones; Adhesives based on derivatives of such polymers
- C09J161/04—Condensation polymers of aldehydes or ketones with phenols only
- C09J161/06—Condensation polymers of aldehydes or ketones with phenols only of aldehydes with phenols
Definitions
- the moisture content of the veneers going through the hot press is greater than about 4%, steam explosions and surface checks are very likely to occur on removing the plywood panels from the press. Furthermore, where the moisture content is above 4%, it is necessary for the veneers to remain in the press for a longer period of time to permit the excess of moisture to escape as steam through the edges of the veneer under the action of the heat of the presses.
- the natural wood veneer to be used in the manufacture of the plywood of my invention is prepared in the usual way by peeling the wood on the lathe and then drying. I' have found, however, that it is desirable to dry the veneer to a moisture content of from 2 to 3 and preferably not over 4%, and then use the veneer in the manufacture of plywood as soon as possible after it leaves the drier. Excess core or cross-banding should be stored in low humidity chambers to maintain as constant a moisture content as possible, since varying moisture contents in the veneers cause delay in the pressing operation. This is particularly true in plants 10- o cated in areas where the climate ofiers a high humidity such that the dry core will take on enough moisture, if left around exposed to the air, to I cause steam pockets in the plywood. Such steam pockets not only tend to produce checks in the finished veneers but make necessary a much longer period of time in the hot presses to counteract.
- the coatings of binder material are preferably sprayed on to the surface of the core under pressure. Due to the roughness of the veneer in peeling on the lathe, especially in the case of the softer wood, and due to the natural defects, such as knots, pitch pockets, checks, and the like, it is very difiicult to produce a uniform film of the binder material by the use of the roll type of spreader. In the spray system of spreading the binder over the core, however, the resulting film is practically uniform and can be dried in properly constructed humidity controlled driers to the correct moisture content.
- the coated core is dried, preferably at a temperature of between and 160 F., to a low moisture content, say from 2 to 4%.
- the second coating of binder material is then sprayed on and the coated core again dried to a low moisture content and thereafter humidified.
- the treated cores are placed in. a humidifier at a temperature, preferably, of from 90 to F., with a relative humidity of from 90% to 100%, and for a period of from 10 to 30 minutes, varying with the thickness of the binder film.
- Humidification of the treated cores in this manner makes it possible to obtain a low moisture content in the body of the core while at the same time securing a uniform and correct moisture content in the surface coating or film of the binder material.
- the body of the core should have a moisture content of preferably between 2 and 4% and thebinder film or coating should contain from 15 to 40% moisture. This result is made possible through the use of a two step coating process, with the intermediate drying of the first coating to cause the second coating to be largely confined to the surface and not penetrate the body of the core.
- the substantial moisture content of the binder film or coating is desirable for the reason that it has a plasticizing effect in the hot pressing operation.
- the core should be laid up between the veneers and placed in the press as quickly as possible.
- the temperature range is preferably from 275 to 300 F. While it is advantageous to use temperatures in the lower range, this naturally means increasing the time of the pressing operation, so that for practical purposes, temperatures of between 315 and 335 F. will generally be found most expedient.
- the pressure ranges between 100 pounds per square inch and 250 pounds per square inch, depending upon the kind of wood from which the veneers are made.
- the hot panels Upon leaving the press, the hot panels contain from 2 to ti /2% of moisture and more moisture must be introduced into them to make the panels suitable for commercial use. Since thermal expansion has taken place in the panels while in the hot presses, sudden cooling would produce checks in the surface veneer. Consequently, the hot panels coming from the presses should be immediately taken to a humidifier, where the panels are stacked between racks and weighted to keep them fiat and subjected to a relative humidity of from 80 to 90% and a temperature of about F.
- the time required for proper humidiflcation of the plywood will, of course, depend upon the thickness, but in general varies between 6 and 12 hours.
- the humidification should be continued until the moisture content of the plywood is between 8 and 12%. This is the normal range for the moisture content of finished plywood, after delivery, for the range of relative humidity occurring in most localities where the .plywood panels are used.
- the aqueous dispersion of the binding material may be prepared from various ingredients capable of forming synthetic resins of a hard, infusible character.
- suitable synthetic resins are those of the phenolic-aldehyde and urea-aldehyde type, or mixtures of a urea and of a phenol with an aldehyde, or polymer of an aldehyde, as described in my copending application above referred to.
- Example 1 Parts by weight I Cresylic acid 1000 Formaldehyde (40% aqueous solution)- 1000 Vegetable protein 200 Caustic soda 160 Soya bean oil 10 Triethanolamine 2 Water "-2400
- the vegetable protein may be a dry extracted soya bean flour, peanut flour, or the like. Such flour is first added to the cresylic acid with constant stirring until a smooth homogeneous mass results.
- the mass is then cooled to 60 F., at which temperature the formaldehyde is added and the whole mixture agitated for 5 minutes.
- the heat of reaction between the various ingredients normally brings the mass up to about 70 to 85 C., where the mass is maintained for about 25 to 35 minutes-Next a cold, 10 B. solution of 60 parts of caustic soda in 2400 parts of water is added to the mass. If desired, the solution may be further diluted by the addition of water without causing a precipitation of the partial condensation product and will remain stable for a long period of time without any increase in viscosity.
- An improved binder solution may be prepared in accordance vith the following example:
- Example 3 After the reaction mixture has been prepared, but before its diluting with the additional water, the partial condensation-product is precipitated by the addition of acidulated water, with constant stirring, and then allowed to settle. After decanting off the supernatant liquor, the soft resin material remaining is washed by the further addition of water' until the mixture shows no acid reaction, after which the resinous mass is dissolved in the caustic soda solution with comstant stirring.
- soya beanflour or peanut flour are incorporated for the purpose of increasing the bonding strengthof the synthetic resin resulting from the reaction between cresylic acid and formaldehyde.
- Other vegetable products rich in protein, cellulose and carbohydrates may be used.
- the caustic soda used aids in increasing the solubility of the initial condensation product producedby the reaction between formaldehyde and cresylic acid, or sodium cresylate.
- the triethanolamine which may be a commercial mixture of tri-, diand mono-ethanolamine, acts as an emulsifying agent to prevent precipitation of the partial condensation product. It is important to note, however, that the final solution of the binder material is a true aqueous solution and not an emulsion or colloidal suspension. The reaction is not carried beyond the point at which the partial condensation product is still water soluble.
- the amount of the aqueous binding solution to be applied to the veneer will depend upon the results desired. Excellent results have been obtained using 0.33 ounce of aqueous binding solution per sq. ft. foreach glue line. In general, it is sufllcient to use between 5 and 15 lbs. of resin forming ingredients, on a dry basis, per M sq. ft. of veneer surface being coated.
- the application of the binding solution in two steps by a pressure spray process, as described, makes it possible to use nearer the minimum amount of binding solution and still obtain a satisfactory bond. 2
- the method of making plywood which comprises applying successive coats of an aqueous solution of a. resinous partial condensation product to a core surface, drying said core after each coating to a moisture content of not substantially over 4%, humidifying the final coating to impart to the coating itself a moisture content of from 15 to 40% and uniting said coated core with a veneer by the application of heat and pressure.
- the method of making plywood which comprises applying a light coating of an aqueous so lution of a resinous condensation product to a core surface, drying said coated core, applying a heavier coating of said aqueous solution to the surface only of said coated core, drying said coated core to a moisture content of between 2 and 4%, humidifying said coated core to impart a substantially increased moisture content to said coating but not to the body of the core and uniting said coated core with a veneer by the application of heat and pressure.
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical And Physical Treatments For Wood And The Like (AREA)
- Veneer Processing And Manufacture Of Plywood (AREA)
Description
Patented Jan. 26, 1937 UNITED STATES METHOD OF MAKING PLYWOOD James V. Nevin, Aberdeen, Wash.
No Drawing. Application August 12, 1935, Serial No. 35,884
4 Claims.
gust 27, 1934, wherein is disclosed a method of making plywood using an aqueous solution of a partial condensation product as the binder.
I have found that in the making of hot pressed plywood, it is very important to control the moisture content of the constituent laminations, and
particularly the core or cross-banding, prior to the hot pressing operation. If the moisture content of the veneers going through the hot press is greater than about 4%, steam explosions and surface checks are very likely to occur on removing the plywood panels from the press. Furthermore, where the moisture content is above 4%, it is necessary for the veneers to remain in the press for a longer period of time to permit the excess of moisture to escape as steam through the edges of the veneer under the action of the heat of the presses.
It is also important to maintain a substantial percentage of moisture in the binder coating on the core, while keeping the moisture content of the body of the core at not over about 4% moisture, at the time of charging the veneers into the hot presses. I have found that this may be best accomplished by applying the aqueous solution of the binder material in successive steps, first applying a light coat and drying rapidly, and then applying a heavier final coat, drying the same and finally humidifying the surface coating to impart thereto a substantial moisture content. By the application of the aqueous binder material in successive steps, penetration of the binder material to the body of the core occurs only during the first coating operation and the second coating of binder material is thereby confined largely to the surface, where it can be most effectively used in the laminating operations.
It is therefore an important object of this invention to provide a method of making nlywood that more effectively utilizes the binding qualities of an aqueous dispersion ofa resin forming partial condensation product, and wherein moisture content of the coated core, or cross-banding, prior to the hot pressing operation is carefully controlled.
It is 'a further important object of this invention to provide an improved method for the manufacture of plywood, using an aqueous dispersion of a partial condensation product and by careful control of the moisture content of the constituent veneers, eliminating the likelihood of steam explosions and surface checks, as well as warping of the finished plywood.
Other and further important objects of this invention will become apparent from the following description and appended claims.
The natural wood veneer to be used in the manufacture of the plywood of my invention is prepared in the usual way by peeling the wood on the lathe and then drying. I' have found, however, that it is desirable to dry the veneer to a moisture content of from 2 to 3 and preferably not over 4%, and then use the veneer in the manufacture of plywood as soon as possible after it leaves the drier. Excess core or cross-banding should be stored in low humidity chambers to maintain as constant a moisture content as possible, since varying moisture contents in the veneers cause delay in the pressing operation. This is particularly true in plants 10- o cated in areas where the climate ofiers a high humidity such that the dry core will take on enough moisture, if left around exposed to the air, to I cause steam pockets in the plywood. Such steam pockets not only tend to produce checks in the finished veneers but make necessary a much longer period of time in the hot presses to counteract.
Where veneers having a higher moisture content than about 4% are used in the hot presses, there is not only a tendency for steam explosions and surface checks to occur, but the cell walls of the wood are rendered much more collapsible, so that when pressure is applied the thickness of the plywood panel is likely to be reduced in varying proportions. It is therefore important to use low moisture content veneers, both in or der to reduce the period of time required in the pressing operation and also to secure a maximum' and more uniform thickness of the final product at identical pressures.
In the preparation of the wood veneers .for the pressing operation, I prefer to apply an aqueous dispersion of the binding material in successive coatings, drying the first applied coating prior to the application of the second coating in order to confine the second coating of the binder material as much as possible to the surface. If only 50 one full coat is applied, it takes longer to dry and permits the binder to penetrate further into the core, resulting in a less effective use of the binder material. Moreover, where a roll type of spreader is used in applying the liquid binder material, the pressure of the rolls tends to force the binder into the wood and leave dry spots.
I have found that by first spreading a light coat of the binder material and drying the coating rapidly, it acts as a filler to close up the pores and crevices of the core, so that when the second coat is applied, it will tend to stay on the surface. Areas not entirely covered by the first coat will be covered by the second coat of binder.
The coatings of binder material are preferably sprayed on to the surface of the core under pressure. Due to the roughness of the veneer in peeling on the lathe, especially in the case of the softer wood, and due to the natural defects, such as knots, pitch pockets, checks, and the like, it is very difiicult to produce a uniform film of the binder material by the use of the roll type of spreader. In the spray system of spreading the binder over the core, however, the resulting film is practically uniform and can be dried in properly constructed humidity controlled driers to the correct moisture content.
After the application of the first light coatin of aqueous binder solution, the coated core is dried, preferably at a temperature of between and 160 F., to a low moisture content, say from 2 to 4%. The second coating of binder material is then sprayed on and the coated core again dried to a low moisture content and thereafter humidified. For this purpose the treated cores are placed in. a humidifier at a temperature, preferably, of from 90 to F., with a relative humidity of from 90% to 100%, and for a period of from 10 to 30 minutes, varying with the thickness of the binder film. Humidification of the treated cores in this manner makes it possible to obtain a low moisture content in the body of the core while at the same time securing a uniform and correct moisture content in the surface coating or film of the binder material. After the humidlfication, the body of the core should have a moisture content of preferably between 2 and 4% and thebinder film or coating should contain from 15 to 40% moisture. This result is made possible through the use of a two step coating process, with the intermediate drying of the first coating to cause the second coating to be largely confined to the surface and not penetrate the body of the core. The substantial moisture content of the binder film or coating is desirable for the reason that it has a plasticizing effect in the hot pressing operation.
After the humidifying treatment is finished, the core should be laid up between the veneers and placed in the press as quickly as possible. There are three main factors to be controlled in hot pressing the cross-banded veneers, namely, temperature, pressure and time. The temperature range is preferably from 275 to 300 F. While it is advantageous to use temperatures in the lower range, this naturally means increasing the time of the pressing operation, so that for practical purposes, temperatures of between 315 and 335 F. will generally be found most expedient. The pressure ranges between 100 pounds per square inch and 250 pounds per square inch, depending upon the kind of wood from which the veneers are made.
On fir, for example, it has been found best to use between and lbs. per sq. in. of pressure on the presses, although the pressure may be increased to as high as 500 lbs. per sq. in. Time, of course, varies with the temperature used and with the thickness of the plywood panel being made. At 330 F. a 15th inch construction requires 2 minutes, a iii/44th inch construction about 20 minutes and an flth inch construction about 36 minutes.
Upon leaving the press, the hot panels contain from 2 to ti /2% of moisture and more moisture must be introduced into them to make the panels suitable for commercial use. Since thermal expansion has taken place in the panels while in the hot presses, sudden cooling would produce checks in the surface veneer. Consequently, the hot panels coming from the presses should be immediately taken to a humidifier, where the panels are stacked between racks and weighted to keep them fiat and subjected to a relative humidity of from 80 to 90% and a temperature of about F.
The time required for proper humidiflcation of the plywood will, of course, depend upon the thickness, but in general varies between 6 and 12 hours. The humidification should be continued until the moisture content of the plywood is between 8 and 12%. This is the normal range for the moisture content of finished plywood, after delivery, for the range of relative humidity occurring in most localities where the .plywood panels are used.
The aqueous dispersion of the binding material may be prepared from various ingredients capable of forming synthetic resins of a hard, infusible character. Examples of suitable synthetic resins are those of the phenolic-aldehyde and urea-aldehyde type, or mixtures of a urea and of a phenol with an aldehyde, or polymer of an aldehyde, as described in my copending application above referred to.
In addition to the examples of aqueous binder solutions given in the aforesaid application, the following will serve to illustrate methods of preparing suitable binder solutions:
Example 1 Parts by weight I Cresylic acid 1000 Formaldehyde (40% aqueous solution)- 1000 Vegetable protein 200 Caustic soda 160 Soya bean oil 10 Triethanolamine 2 Water "-2400 The vegetable protein may be a dry extracted soya bean flour, peanut flour, or the like. Such flour is first added to the cresylic acid with constant stirring until a smooth homogeneous mass results. A 38 B. solution of caustic soda, containing about 100 parts of caustic soda, is added to the mixture of cresylic acid and soya bean or the vegetable flour. Then the soya. bean oil and triethanolamine are added and the mixture agitated until a smooth homogeneous mass results. The mass is then cooled to 60 F., at which temperature the formaldehyde is added and the whole mixture agitated for 5 minutes. The heat of reaction between the various ingredients normally brings the mass up to about 70 to 85 C., where the mass is maintained for about 25 to 35 minutes-Next a cold, 10 B. solution of 60 parts of caustic soda in 2400 parts of water is added to the mass. If desired, the solution may be further diluted by the addition of water without causing a precipitation of the partial condensation product and will remain stable for a long period of time without any increase in viscosity.
In making up this second formula, 60 parts of caustic soda are dissolved in order to form a 30 B. solution and this solution then added to the cresylic acid and mixed thoroughly therewith. The mixtureis allowed to cool to 60 F., at which temperature the soya bean oil and triethanolamine are added. The formaldehyde is next added and the' mixture agitated. The heat of reaction between the-various ingredients brings the mass up to a temperature of normally from 70 to 90 'C. After maintaining the mass at this temperature for about 25 to 35 minutes, the remaining portion of caustic soda; namely 36 parts, dissolved in 1500 parts of water and having a specific gravity of about 10 B., is added to the mixture with constant stirring until -cold. As before, the solution may be diluted further by the addition of water without causing a precipitation of the partial condensation product. The final mixture is a clear amber colored solution and will remain stable for a long period of time without any increase in viscosity.
An improved binder solution may be prepared in accordance vith the following example:
Example 3 After the reaction mixture has been prepared, but before its diluting with the additional water, the partial condensation-product is precipitated by the addition of acidulated water, with constant stirring, and then allowed to settle. After decanting off the supernatant liquor, the soft resin material remaining is washed by the further addition of water' until the mixture shows no acid reaction, after which the resinous mass is dissolved in the caustic soda solution with comstant stirring.
By the method of Example 3, all the impurities are removed from the resin, so that when the resin is brought back into solution, the mixture is much lighter in color and holds for a much longer period of time without any increase in viscosity.
In Examples 1 and 2, soya beanflour or peanut flour are incorporated for the purpose of increasing the bonding strengthof the synthetic resin resulting from the reaction between cresylic acid and formaldehyde. Other vegetable products rich in protein, cellulose and carbohydrates may be used.
It. will be understood that the proportions of the various ingredients in the formulae of Examples 1 and 2 may. be varied considerably and other ingredients substituted for those enumerated, as more fully explained in my copending application above referred to. The caustic soda used aids in increasing the solubility of the initial condensation product producedby the reaction between formaldehyde and cresylic acid, or sodium cresylate. The triethanolamine, which may be a commercial mixture of tri-, diand mono-ethanolamine, acts as an emulsifying agent to prevent precipitation of the partial condensation product. It is important to note, however, that the final solution of the binder material is a true aqueous solution and not an emulsion or colloidal suspension. The reaction is not carried beyond the point at which the partial condensation product is still water soluble.
The amount of the aqueous binding solution to be applied to the veneer will depend upon the results desired. Excellent results have been obtained using 0.33 ounce of aqueous binding solution per sq. ft. foreach glue line. In general, it is sufllcient to use between 5 and 15 lbs. of resin forming ingredients, on a dry basis, per M sq. ft. of veneer surface being coated. The application of the binding solution in two steps by a pressure spray process, as described, makes it possible to use nearer the minimum amount of binding solution and still obtain a satisfactory bond. 2
I am aware that numerous details of the process may be varied through a wide range without departing from the principles of this invention, and I, therefore, do not purpose limiting the patent granted hereon otherwise than necessitated by the prior art.
I claim as my invention:
1. The method of making plywood which comprises applying successive coats of an aqueous solution of a. resinous partial condensation product to a core surface, drying said core after each coating to a moisture content of not substantially over 4%, humidifying the final coating to impart to the coating itself a moisture content of from 15 to 40% and uniting said coated core with a veneer by the application of heat and pressure.
2. The method of making plywood which comprises applying a light coating of an aqueous so lution of a resinous condensation product to a core surface, drying said coated core, applying a heavier coating of said aqueous solution to the surface only of said coated core, drying said coated core to a moisture content of between 2 and 4%, humidifying said coated core to impart a substantially increased moisture content to said coating but not to the body of the core and uniting said coated core with a veneer by the application of heat and pressure.
3. The method of making plywood which com-- prises applying a light coating of aqueous solution of a partial condensation product of cresylic acid and an aldehyde to a core surface, drying said coated core, applying a heavier coating of said aqueous solution to the surface only,of said coated core, drying said coated core to a moisture content of between 2 and 4%, humidiiying said coating on the core to impart a substantially increased moisture content to said coating, but not to the body of the core, uniting said coated core with a veneer by the application of heat and surface coating thereof a moisture content of be tween 15 and 40% and uniting said coated core with a veneer by the application of heat and pressure.
JAMES V. NEVIN.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US35884A US2068759A (en) | 1935-08-12 | 1935-08-12 | Method of making plywood |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US35884A US2068759A (en) | 1935-08-12 | 1935-08-12 | Method of making plywood |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US2068759A true US2068759A (en) | 1937-01-26 |
Family
ID=21885356
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US35884A Expired - Lifetime US2068759A (en) | 1935-08-12 | 1935-08-12 | Method of making plywood |
Country Status (1)
| Country | Link |
|---|---|
| US (1) | US2068759A (en) |
Cited By (13)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2459851A (en) * | 1941-12-31 | 1949-01-25 | Masonite Corp | Ligno-cellulose die-stock and process of making |
| US2563821A (en) * | 1945-07-25 | 1951-08-14 | Koppers Co Inc | Laminating wood |
| US2565251A (en) * | 1948-04-30 | 1951-08-21 | Paper Patents Co | Plywood panel |
| US2574784A (en) * | 1944-12-26 | 1951-11-13 | Weyerhaeuser Timber Co | Phenolic adhesive and method of bonding wood plies |
| US2626934A (en) * | 1948-11-17 | 1953-01-27 | Penick & Ford Ltd Inc | Alkaline-setting resin adhesive and method of making same |
| US2631097A (en) * | 1948-11-04 | 1953-03-10 | American Marietta Co | Method of producing cellulose mass and product |
| US2631098A (en) * | 1948-11-04 | 1953-03-10 | American Marietta Co | Production of thermosetting phenol-aldehyde resin condensation products |
| US2635066A (en) * | 1949-11-21 | 1953-04-14 | Plywood Res Foundation | Method of producing plywood |
| US2946713A (en) * | 1955-10-06 | 1960-07-26 | Gen Motors Corp | Process for embossing decorative articles |
| US3005743A (en) * | 1957-08-09 | 1961-10-24 | Dow Chemical Co | Method for joining wood articles with resinous coal acids adhesives |
| US3052587A (en) * | 1957-10-08 | 1962-09-04 | Gen Motors Corp | Dielectric embossing |
| USD739739S1 (en) | 2014-09-11 | 2015-09-29 | Mary Kay Inc. | Cosmetic container |
| USD739741S1 (en) | 2013-06-20 | 2015-09-29 | Mary Kay Inc. | Cosmetic container |
-
1935
- 1935-08-12 US US35884A patent/US2068759A/en not_active Expired - Lifetime
Cited By (18)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2459851A (en) * | 1941-12-31 | 1949-01-25 | Masonite Corp | Ligno-cellulose die-stock and process of making |
| US2574784A (en) * | 1944-12-26 | 1951-11-13 | Weyerhaeuser Timber Co | Phenolic adhesive and method of bonding wood plies |
| US2563821A (en) * | 1945-07-25 | 1951-08-14 | Koppers Co Inc | Laminating wood |
| US2565251A (en) * | 1948-04-30 | 1951-08-21 | Paper Patents Co | Plywood panel |
| US2631097A (en) * | 1948-11-04 | 1953-03-10 | American Marietta Co | Method of producing cellulose mass and product |
| US2631098A (en) * | 1948-11-04 | 1953-03-10 | American Marietta Co | Production of thermosetting phenol-aldehyde resin condensation products |
| US2626934A (en) * | 1948-11-17 | 1953-01-27 | Penick & Ford Ltd Inc | Alkaline-setting resin adhesive and method of making same |
| US2635066A (en) * | 1949-11-21 | 1953-04-14 | Plywood Res Foundation | Method of producing plywood |
| US2946713A (en) * | 1955-10-06 | 1960-07-26 | Gen Motors Corp | Process for embossing decorative articles |
| US3005743A (en) * | 1957-08-09 | 1961-10-24 | Dow Chemical Co | Method for joining wood articles with resinous coal acids adhesives |
| US3052587A (en) * | 1957-10-08 | 1962-09-04 | Gen Motors Corp | Dielectric embossing |
| USD739741S1 (en) | 2013-06-20 | 2015-09-29 | Mary Kay Inc. | Cosmetic container |
| USD795074S1 (en) | 2013-06-20 | 2017-08-22 | Mary Kay Inc. | Cosmetic container |
| USD843835S1 (en) | 2013-06-20 | 2019-03-26 | Mary Kay Inc. | Cosmetic container |
| USD739739S1 (en) | 2014-09-11 | 2015-09-29 | Mary Kay Inc. | Cosmetic container |
| USD795075S1 (en) | 2014-09-11 | 2017-08-22 | Mary Kay Inc. | Cosmetic container |
| USD844441S1 (en) | 2014-09-11 | 2019-04-02 | Mary Kay Inc. | Cosmetic container |
| USD865525S1 (en) | 2014-09-11 | 2019-11-05 | Mary Kay Inc. | Cosmetic container |
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