AU2002312503A1 - Novel phenol-aldehyde/wax emulsion adhesive - Google Patents
Novel phenol-aldehyde/wax emulsion adhesiveInfo
- Publication number
- AU2002312503A1 AU2002312503A1 AU2002312503A AU2002312503A AU2002312503A1 AU 2002312503 A1 AU2002312503 A1 AU 2002312503A1 AU 2002312503 A AU2002312503 A AU 2002312503A AU 2002312503 A AU2002312503 A AU 2002312503A AU 2002312503 A1 AU2002312503 A1 AU 2002312503A1
- Authority
- AU
- Australia
- Prior art keywords
- wax
- phenol
- emulsion
- formaldehyde
- aldehyde
- 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.)
- Abandoned
Links
Description
NOVEL PHENOL- ALDEHYDE/WAX EMULSION ADHESIVE
BACKGROUND OF THE INVENTION
1. Field of the Invention
This invention relates generally to the field of adhesives and, more specifically, to a
nonionic surfactant for producing stable emulsions in a phenol-aldehyde/wax emulsion
environment.
2. Description of the Related Art
The use of adhesives, especially phenol-aldehyde resole resins, to bind wood particles
into a unitary mass is generally well known. Many useful wood products, including oriented
strandboard (OSB), chipboard or particle board can be made by coating the wood particles
with a phenol-aldehyde resin, and consolidating the particles, usually under heat and pressure,
into a unitary mass.
However, the need has been recognized to impart water resistance to such wood
products, such as by the incorporation of a wax into the product. However, wax does not
form a stable emulsion in the presence of a phenol-aldehyde resin.
Recently, it has been discovered that phenol-aldehyde resins can be made into a stable
emulsion if an anionic emulsifier, such as a lignosulfonate, e.g., sodium lignosulfonate, is
added to the blend of wax and phenol-aldehyde. This anionic emulsifier is shear sensitive, as
well as resin sensitive. Furthermore, anionic emulsifiers do not exhibit storage stability beyond
a short term, e.g., on the order of one day.
The first attempt to solve long-term stability problems of a phenol-aldehyde/wax
emulsion was to modify the pH of the phenol-aldehyde, wax emulsion by forming an adjusted pH resin of between 9 and 12, adjusting the pH of the wax emulsion to within 1 pH unit of the
resin, and combining the same, with mixing, at a temperature of the resin above 40°C; See,
U.S. Patent 6,132,885.
Further attempts to solve the problem of phenol-aldehyde, wax emulsion stability can
be found in U.S. Patent 6,028,133, which incorporates a cationic surfactant, such as an alkali
salt of sulfite or bisulfite, into a phenolic resin so as to obtain a resin with anionic character.
However, this process also proved not to be fully effective as it was both resin and wax
sensitive. The disclosures of the above-mentioned U.S. Patents are herein incorporated by
reference in their entirety.
However, despite these attempts to provide a stable emulsion, there continues to be a
need for a phenol-aldehyde wax emulsion that is much more shear stable than a lignin based
emulsion and which provides long term stability, nor use the ionic surfactants of the above-
mentioned systems with their attendant disadvantages.
SUMMARY OF THE INVENTION
The present inventors have developed non-lignin based and non-ionic emulsion
systems that provide stability to phenol-aldehyde, wax emulsions.
The present invention permits the use of a wider variety of phenolic resins than that
permitted in the aforementioned U.S. Patents, as well as a wider variety of raw waxes, with improved shear stability.
These and other attributes of the invention will be seen in connection with the
following detailed description of the preferred embodiments.
DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS
The various resins suitable for use in the invention are termed phenol-aldehydes which
is meant to describe thermosetting resins formed from a phenol or phenol contributing
substance and a methylene donor, such as formaldehyde.
Generally, the phenol or phenol contributing substance includes phenol, resorcinol,
hydroquinone, cresols and other phenol derivatives, such as xylenols, catechol, cresylic acids,
urea, melamine and combinations thereof.
The methylene donor can be formaldehyde, paraformaldehyde, formalin, acetaldehyde,
propionaldehyde, and similar substances.
Suitable resins include phenol-formaldehyde, phenol-resorcinol-formaldehyde, urea-
melamine formaldehyde, melamine-formaldehyde, phenol-melamine-formaldehyde, melamine- urea-resorcinol formaldehyde, resorcinol-formaldehyde and combinations thereof.
The wax emulsion (also known as a paraffin emulsion) can be formed from a variety of
naturally occurring waxes, such as slack wax, shale wax, poppy wax, honey wax and Chinese
wax or from synthetic waxes such as esters of fatty acids, such as n-octadecyl palmitate and
cetyl stearate. Slack wax, a byproduct of petroleum refining, is preferred.
Typical formulations can be seen in the following exemplary compositions. All
percentages are in parts by weight unless otherwise indicated.
Example 1
Raw Material %
1) 100% phenol 25.0
2) Water 15.28
3) 50% sodium hydroxide 2.50
4) 50% formaldehyde 31.92
5) 50% sodium hydroxide 6.00
6) 50% sodium hydroxide 3.50
7) Urea 2.50
8) Cascowax EW-58NI 13.30
1) Charge phenol (1), water (2) and sodium hydroxide (3). Exotherm to 55-60°C
2) At > 55°C, program formaldehyde (4) over 35-45 minutes while exotherming to 81°C
3) Hold at 81°C for 10 minutes after formaldehyde is in
4) Charge sodium hydroxide (5) over 8-10 minutes while exotherming to 92°C
5) Condense at 92°C to a Gardner viscosity "D/E" of about 110 cps.
6) At "D/E" cool to 81°C and charge sodium hydroxide (6)
7) Hold at 81°C to "M/N" viscosity
8) Cool to 75°C and react to a Gardner viscosity "W/X" of about 1180 cps.
9) At "W/X" cool to 70°C and charge Urea. Let mix 5-10 minutes
10) Charge EW-58NI wax emulsion between 63 and 65°C
11) Cool to shipping or storage temp.
Solids = 49-51% Alkalinity = 5.8-6.2% 100°C Gel time = 30-34 minutes Viscosity = 400-600 cps.
In the foregoing example, "Cascowax EW58NI" is the description for a non-ionic wax
emulsion formed of the following composition.
Example 2
Slack wax (paraffin) 53.22%
Protachem SG Blend 4.68%
Water 42.00%
Nopco NXZ 0.10%
The emulsifier, Protachem SG Blend, is a blend of POE (20) Stearyl Alcohol (CAS #9005-00- 0) and Glyceryl Monostearate (CAS # 123-94-4). The wax emulsion is made in the same process used for our other wax emulsions, with the new emulsifier. This produces a non-ionic emulsion that is stable when mixed with phenolic resin. The Nopco NXZ is a defoamer, one of several that could be used.
Although we have described the phenol-aldehyde/wax emulsion as providing utility for forming OSB or other particle board, the adhesive is not to be construed as so limited. The adhesive of the invention has general utility for any lignocellulose based substrate such as plywood, laminated veneer lumber (LVL), high density fiber board(HDF) and medium density fiber board (MDF) and other composites.
Claims (20)
1. An emulsion of a phenol-aldehyde and wax comprising:
phenol-aldehyde, wax; and an emulsion stabilizing effective amount of a non-ionic surfactant.
2. The emulsion of claim 1, wherein the non-ionic surfactant comprises
polyoxyethylene (POE), stearyl alcohol and glyceral monostearate.
3. The emulsion of claim 1, further comprising an aqueous portion.
4. The emulsion of claim 3 , wherein the aqueous portion comprises water and at least
one component selected from the group consisting of a defoamer and pH regulating agents.
5. The emulsion of claim 1, wherein the phenol-aldehyde consists of at least one
material selected from the group consisting of phenol-formaldehyde, phenol-resorcinol-
formaldehyde, urea-melamine formaldehyde, melamine-formaldehyde, phenol-melamine-
formaldehye, melamine-urea-resorcinol formaldehyde, and resorcinol-formaldehyde.
6. The emulsion of claim 5, wherein the wax is selected from natural and synthetic
waxes.
7. The emulsion of claim 6, wherein the wax is one selected from the group
consisting of slack wax, shale wax, poppy wax, honey wax, Chinese wax, and esters of fatty acids.
8. An adhesive comprising the emulsion of claim 1.
9. Bonded wood products comprising particles of a lignocellulosic material bond
together with the adhesive of claim 8.
10. The bonded wood products of claim 9, wherein the wood products are at least one
selected from the group consisting of oriented strandboard, particle board, chipboard, laminated
veneer lumber, plywood, high density fiberboard and medium density fiberboard.
11. A method of stabilizing a phenol-aldehyde/wax emulsion, said method comprising:
combining a non-ionic surfactant with a phenol-aldehyde and wax to form a stabilized
phenol-aldehyde/wax emulsion.
12. The method of claim 11, wherein the non-ionic surfactant comprises
polyoxyethylene (POE), stearyl alcohol and glyceryl monostearate.
13. The method of claim 11 , wherein the phenol-aldehyde is at least one selected from
the group consisting of phenol-formaldehyde, phenol-resorcinol-formaldehyde, urea-melamine
formaldehyde, melamine-formaldehyde, phenol-melamine-formaldehyde, melamine-urea-
resorcinol formaldehyde, and resorcinol-formaldehyde.
14. The method of claim 13, wherein the wax is a natural or synthetic wax.
15. The method of claim 14, wherein the wax is at least one selected from the group
consisting of slack wax, shale wax, poppy wax, honey wax, Chinese wax, and esters of fatty acids.
16. The method of claim 13, wherein the wax is slack wax.
17. The method of claim 11 , further comprising binding wood particles together with
an adhesive formed from the stabilized emulsion.
18. The method of claim 17, wherein the wood particles are formed into at least one
product selected from the group consisting of oriented strandboard, particle board, chipboard,
laminated veneer lumber, plywood, high density fiberboard and medium density fiberboard.
19. The emulsion of claim 5, wherein the wax is slack wax.
20. Bonded wood products made by the method of claim 17.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US60/298,125 | 2001-06-15 |
Publications (1)
Publication Number | Publication Date |
---|---|
AU2002312503A1 true AU2002312503A1 (en) | 2003-01-02 |
Family
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