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.