GB2538060A

GB2538060A - Improving fire retardant properties of wood

Info

Publication number: GB2538060A
Application number: GB1507324.0A
Authority: GB
Inventors: Arbache Simon
Original assignee: PFS COATINGS Ltd
Current assignee: PFS COATINGS Ltd
Priority date: 2015-04-29
Filing date: 2015-04-29
Publication date: 2016-11-09
Anticipated expiration: 2035-04-29
Also published as: GB201507324D0; GB2538060B; WO2016173743A1; EP3288732A1; GB2538060A8

Abstract

A method for improving fire retardant properties of an item of wood including the steps of: a) providing an item of wood to be treated; b) if the wood has a moisture content of greater than 20%, drying the wood so that it has a moisture content no greater than 20%; c) coating a first major surface of the item of wood with a first coating formulation including an aqueous solution containing boric acid or a salt thereof, an amine or ammonium salt, and a phosphate; d) repeating steps b) and c) and b); e) coating the first major surface with a second coating formulation including a film-forming polymer material in an aqueous carrier. The first coating may include an adjuvant such as a glycol. The film-forming polymer may be a styrene butadiene copolymer. The second coat may include a UV-protecting agent, a material such as silicon dioxide for increasing surface hydrophobicity and a crosslinking agent such as a zinc salt.

Description

IMPROVING FIRE RETARDANT PROPERTIES OF WOOD

BACKGROUND

a. Field of the Invention

The invention relates to a method for improving fire retardant properties of an item of wood, and to an item of wood having at least a major surface with fire-retardant properties.

Various standards are recognised in the timber and building industries for fire retardant properties of timber for use in building. It is particularly desirable that wood meet the Class B fire retardancy standard, as tested under BS EN 13823:2010. This Single Burning Item (SBI) test simulates the conditions experienced by a construction product in the corner of a room, when exposed to the thermal attack of a single burning item positioned in that corner. BS EN 13823:2010 is included within the testing protocol EN 13501-1:2007+A1:2009, Fire Classification of Construction Products and Building Elements.

European legislation around the Construction Products Regulation, using EN 13986 has mandated that for a product to carry a CE mark it must be supported by a Declaration of Performance (DoP) Certificate which lists the relevant performance of that product in terms usable by the builder/engineer/specifier/architect. The DoP is created and owned by the manufacturer and passed on to any subsequent owners so long as the product itself has not been changed in any way.

EN 13986:2004 is the harmonised European standard for wood-based panels. It defines the performance characteristic and test methods for wood-based panels (including plywood, oriented strand board, and laminated veneer lumber) enabling their use in construction applications. A series of tables lists the relevant performance characteristics for load-bearing (structural) and non-structural applications in the three service environments: dry, humid and exterior. -2 -

With pressure treatment to improve fire retardant (FR) properties, the wood owner who has made the change to the FR of the product can improve the EN13501-1 class on the DoP from usually Class D s2 dO to whatever they have achieved though independently verified testing, for instance Class B or C, 51 or 2, dO. As it is not then known how the product has been changed in terms of strength, bonding quality etc, the wood owner must remove all other data on the DoP and replace it with NPD (No Performance Declared). This removes any claim of structural use. If the panel was CE marked as suitable for structural use with a AVCP Class 2+ (CE2+) before hand, it will be dropped down to Class 1 which is non-structural and they must legally declare as such to the next owner.

The only way that the owner can return the product to being defined as CE2+ structural is to prove to the original manufacturer that they have not changed the properties of the boards, which given the aggressive physics involved, is highly improbable. It may well be that the manufacturer can introduce FR into their own production process and therefore do their own testing with the improved fire resistance already present, but it is not possible for a post-production pressurised treatment to do this.

b. Related Art Various treatments are known for improving fire retardant properties of wood, including pressure treatments, often in conjunction with improvements to other properties such as mould resistance or insect resistance. US 2005/0217537 discloses a composition for rendering a material flame retardant and resistant to moulds and insects. The composition comprises a metallic borate, a methyl donor, an acid, an alcohol, and an ammonium base. -3 -

SUMMARY OF THE INVENTION

Aspects of the invention are specified in the independent claims. Preferred features are specified in the dependent claims.

We have surprisingly found that by using a double coating of borate, amine or ammonium ions, and phosphate ions, in combination with a top coat of a film-forming polymer material, it is possible to improve flame retardant properties of wood, and to achieve Class B fire retardancy standard, as tested under BS EN 13823:2010. The use of an adjuvant is particularly beneficial because this promotes homogenous spreading and penetration of the fire retardant treatment into the wood.

The boric acid or borate may be provided in an ammoniated salt, which is particularly water soluble and also provides an ammonium source.

The adjuvant may comprise one or more of: a glycol, a hydrotrope, and a surfactant. The term 'hydrotropei is used herein to refer to a compound that solubilises hydrophobic compounds in aqueous solutions. Typically, hydrotropes consist of a hydrophilic part and a hydrophobic part (like surfactants) but the hydrophobic part is generally too small to cause spontaneous self-aggregation The second coating formulation provides a film which we refer to as a MicroBarrier. Without wishing to be bound by theory, we believe that application of the MicroBarrier seals salts therein by creating a hydrophobic and moisture-resistant film, aiding retention of salts within a matrix in the wood.

The first formulation and the second formulation may be coated onto the wood surface by any suitable application techniques, notably by spray application or by roller application. -4 -

DETAILED DESCRIPTION

Solution 1, containing boric acid and diammonium phosphate was prepared a follows.

Chemical name EC /CAS Number Content per Litre Boric Acid EC: 233-139-2 63.45 g Diammonium Phosphate EC: 231-987-8 405.2 g Water 760g Solution 1 Manufacturing Method 1. To a clean tank charge with required amount warm (ca. 30°C) water; 2 Begin stirring; 3 Add required amount of Boric Acid and stir; 4 Add Diammonium Phosphate and stir; 5 Continue stirring until product fully dissolved, clear and free from insoluble material; 6. When filling, filter with a 100 pm filter.

Solution 2, containing adjuvant materials to promote wetting and aid penetration of wood, was made up as follows. -5 -

Formulation Chemical name EC /CAS Number Content EC: 203-905-0 Butyl Glycol 500 grams CAS: 111-76-2 Phenol ethoxylate (4 Mol) Phosphate Ester, Potassium Salt CAS: 72283-31-9 250 grams Solution 65% Solution d-glucopyranose, oligomers, CAS: 68515-73-1 250 grams decyl -octyl glycosides Solution 2 Manufacturing Method 1. To a clean tank charge with Butyl Glycol and Phenol Ethoxylate Phosphate Ester Salt in that order and stir; 2. Stir until homogenous and add remaining ingredients; 3. Stir a final time for 20 minutes.

First Coating Formulation A first coating formulation was prepared by mixing Solution 1 and Solution 2 in a 95:5 volume ratio (116.7:4.85 weight ratio). Moderate agitation was maintained throughout the process to prevent phase separation.

Second Coating Formulation A second coating formulation was prepared as follows. -6 -

Chemical name EC /CAS Number Content Styrene Butadiene Copolymer CAS: 9003-55-8 500 grams Solution, Grade CLI 3008 Butyl Glycol EC: 203-905-0 100 grams CAS: 111-76-2 Phenol ethoxylate (4 Mol) CAS: 72283-31-9 25 grams Phosphate Ester, Potassium Salt Solution 65% Solution Zinc Oxide CAS: 1314-13-2 1 gram Titanium Oxide CAS: 236-675-5 1 gram Silicon Oxide CAS: 231-545-4 1 gram Water 375 grams Second Coating Formulation Manufacturing Method 1. To a clean tank charge with required amount cool (ca. 20°C) water; 2. Begin stirring; 3. Add CLI 3008, Butyl Glycol and Phenol Ethoxylate Phosphate Ester Salt in that order and stir; 4. Stir until homogenous and add remaining ingredients; 5. Stir a final time for 20 minutes. -7 -

Example 1

The first coating formulation was spray coated onto a substrate of Wisa Finnish Spruce Plywood 2440 mm x 1220 mm (8' x 4') 18 mm thick, 7 veneer, under the conditions summarised in Table 1.

Equipment running 3 metres! minute speed Pre-heat oven 6 x IR lamps at 80 °C each Combination dryer Gas at 64°C 2 x IR @ 70 °C; IR @ 80 °C; 2 x IR @ 90°C UV Curing None

Table

Ambient temperature and relative humidity may require the specifications to be changed. Increase / modify the combination dryer as necessary to yield a dry wood at the end.

1 Calibrate machine to apply 260 g/m2 ± 5 g/m2 of the first coating formulation described above. This equates to 32.5 grams on an 1/8th m2 tester board 2. Verify scale-up on first board passed, record weight.

Weight increase of a 2440 mm x 1220 mm (8' x 4') board is 772.95 g / board ± 14.9 grams 3. Allow the machine to warm up to the specifications above 4. Once verified, load the wood into the machine and run through to apply the fire retardant.

Surface 1, Pass 1 Before proceeding, the operator checks that the wood is dry. Randomised wood moisture content must be no more than 20% measured using a wood moisture meter. If necessary, the wood is dried to a moisture content of no more than 20%, preferably about 15%.

Surface 1, Pass 2 After the first coating pass, the same process is repeated for the second pass, with measured moisture content of the wood being no more than 20%, preferably about 15%, prior to the second coating pass.

Typically after drying in a rack for at least 24 hours (or longer depending on ambient temperature and humidity) the panel is rotated, and Surface 2 is treated with the same two-pass coating process as was done for Surface 1.

In this embodiment, each coating pass applies the first coating formulation at a 20 rate of about 260 g/m2.

After further drying, until the measured wood moisture content is no greater than 20%, preferably about 15%, the second coating formulation is applied to each major surface of the wood, in this example using the process conditions summarised in Table 2. It is important to control the moisture content, because we have found that high surface moisture hinders the MicroBarrier from adhering to the surface. With too high a moisture content prior to coating, the MicroBarrier may flake off after drying. -9 -

Machine specifications:

Equipment running 5 metres! minute speed Pre-heat oven None Combination dryer Gas at 60°C x IR @ 60°C UV Curing None

Table 2

1. Calibrate machine to apply 100 g/m2 ± 5 g/m2 of the combined solution described above. This equates to 12.5 grams on an 1/8th m2 tester board; 2. Verify scale-up on first board passed, record weight.

Weight increase of 2440 mm x 1220 mm (8' x 4') board is 297.3 g / board ± 14.9 grams; 3. Once verified, load the treated wood into the machine and run through to apply the MicroBarrier 4. Flip 1800; Return to the start for treatment, 6. Load the panel and run through to apply the MicroBarrier on the second side; 7. Stack with spacers and allow 2 days for final drying/curing.

Samples of the treated wood were tested at an independent laboratory as detailed in Table 3. Results are summarised in Table 4 and Table 5.

-10 -

Table 3

Table 4

Two tests were performed on each layer The worst performing layer was identified and four further tests were performed on that layer in accordance with EGOLF recommendation ER 07:2003.

Test Reports Extended poication results PFS Coatings Ltd BMT/RFP/ F14116/01 PFS Coatings Ltd BMT/RFP/ F14116/02 BS EN ISO 11925-2:2010

BM TRADA

BS EN 13823:2010

BM TRADA

Numbe of tests and report number ults Compliance with ameters for classification arneter -mean BS EN ISO 11925-2:2010 BMT/RFP/ F14116/01 Fs (flame spread) Flaming droplets/ particles Fs 150mm within 60s No ignition of filter paper compliant compliant 305 exposure surface test Clause 7.3.3.1 30s exposure edge test Clause 7.3.3.2.2 BMT/RFP/ F14116/01 Fs (flame spread) Flaming droplets/ particles Fs 150mm within 60s No ignition of filter paper compliant compliant 30s exposure edge test Clause 7.3.3.2.3 BMT/RFP/ F14116/01 Fs (flame spread) Flaming droplets/ particles Fs 150mm within 60s No ignition of filter paper compliant compliant BS EN 13823:2010 BS EN 3 FIGRA 0.2 MJ 110.5 compliant 13823:2010 BMT/RFP/ F14116/02 LFS None compliant (to edge of specimen) THR 600s 7.5 compliant SMOGRA 7.5 compliant TSP 600s 48.0 compliant Flaming droplets/ None compliant particles

Table 5

Wood treated in accordance with the method of the invention was compliant with BS EN 13823:2010 and also with BS EN ISO 11925-2:2010, which describes methods of test for evaluating linear joint (gap) seals.

It will be appreciated that the invention is not limited to the use of only two applications of the first coating formulation. If desired, further coatings of the first coating formulation may be applied, with drying between the further applications if necessary, to ensure that the moisture content of the wood is no more than 20%, prior to application of the second coating formulation.

It will also be appreciated that more than one application of the second coating formulation may be made, with drying before the second application if necessary, to reduce the moisture content of the wood to no more than 20%.

The preferred first coating formulation is a blend of about 0.9 % B, about 7.0 % N and about 7.73 % P, though the invention is not limited to these ratios. The relative ratios make a significant impact on the fire retardant performance.

We have found that styrene-butadiene copolymers as the MicroBarrier provide an 25 optimum performance compared to all other options.

-12 -Polyacrylate adhesives for example can impart the binding and durability properties required; however the wood panels will be glued together and prevent use. Polyurethanes could also be used; however this was not a viable option for the methods of use of the present examples.

Vinyl chloride was also tested; however this was grossly incompatible with all chemistry tested. It was also on a list of restricted substances. Additives could have been added to impart fire retardance by making use of the halogen; however this would have increased smoke output and made the product not suitable for indoor use.

Styrene-Butadiene copolymers can have a range of properties depending on the ratio of styrene to butadiene monomers, as well as whether the product is post-modified. The grade chosen provides a non-tacky finish, hydrophobic finish and good adhesion into the wood, without increasing smoke output. It also did not cause flaming droplets, something that foaming MicroBarriers such as polyurethane could have caused.

It is desirable to incorporate a zinc salt, notably zinc oxide in the second coating 20 formulation as it promotes the crosslinking of the butadiene component of the styrene-butadiene copolymers upon drying, and reduces tackiness.

Silicon dioxide has reported uses in providing surface hydrophobicity, and further improving the durability of the fire retardant.

Titanium dioxide, albeit in small quantities, provides UV protection and prevents the long term photolysis of the styrene-butadiene copolymer. Styrene-butadiene is a very large chromophore, conjugated or not depending on the molecular construct, and some protection against UV damage is desirable.

-13 -Mechanisms of action Without wishing to be bound by theory, we believe that the following proposed mechanisms are involved in the fire retardant performance of the invention. Boron

Boron will react with hydroxyl (-OH) functional groups of cellulose in wood. The chemical reaction (endothermic) will form a glassy ester that coats the surface and reduces degradation into flammable gases whilst simultaneously releasing water (H20) which provides a cooling effect. Boron (as boric or borate species) will also catalyse the dehydration of wood, catalysing the char formation if synergistic substances (e.g phosphate, P043-) are present.

Phosphorus Phosphate species (e.g. ammonium phosphate) will thermally decompose to release phosphoric acid. Ammonium phosphate will also release ammonia gas (see below). The phosphoric acid will extract water from the pyrolysing substrate, causing char build-up. This mechanism is a combination of dehydration of cellulose (-OH groups) by forming ester bonds, similar to boron, decomposition and release of char (i.e. carbon material). Phosphate-based fire retardants act directly in the pyrolysing stage of fire, reducing the available flammable gas to continue propagation and forming a protective char layer.

The char layer provides a non-combustible thermally insulating layer.

Nitrogen Nitrogen is present in the formulation in its ammoniacal (NH4) form. Unlike the other components, ammonia has a diluent property only. Exposure to high temperatures will cause degradation of the ammonia salts (endothermic) and release of ammonia gas which dilutes the flammable gases. The nitrogen could be present as an amine group, such as those found in Melamine, which can then decompose to yield ammonia.

-14 -Structural Integrity With the present invention, we have created a product that is balanced in terms of FR efficacy, lifetime durability of the coating against weathering/humidity AND retains the structural integrity as CE2+ that is lost to pressure treatment. Due to the chemistry and low/no pressure factory production application method, the boards are not physically damaged by the ingress and we have had BM TRADA as a UKAS body perform extensive testing to ensure that the key numbers have not been changed significantly. The chemistry and its application method do not affect the structural properties of the structural engineered wood-based panels; something which is unique in the industry.

Non-factory production FR 'systems' such as intumescent paints are able to claim FR efficacy but these coatings are applied after the boards have been used within the build environment over which there is far less control in the application and the actual classification offered is usually flawed by this.

Durability Durability is determined by TS 15912:2012 -Durability of reaction to fire performance -Classes of fire-retardant wood-based product in interior and exterior end use applications. This standard is due to be adopted as EN16755 after a public consultation period has been completed. Wood treated according to the present invention has been tested and demonstrated INT2 Durability: for permanent use in interior applications and certain protected exterior applications, service class 2 (eg wall and ceiling products).

Claims

-15 -CLAIMS: 1. A method for improving fire retardant properties of an item of wood, the method comprising: a) providing an item of wood to be treated; b) if the wood has a moisture content of greater than 20%, drying the wood so that it has a moisture content no greater than 20%; c) coating a first major surface of the item of wood with a first coating formulation comprising an aqueous solution containing boric acid or a salt thereof, 10 an amine or ammonium salt, and phosphate; d) repeating steps b) and c) and b); and then e) coating the first major surface with a second coating formulation comprising a film-forming polymer material in an aqueous carrier.
2. A method according to claim 1, wherein the first coating formulation further comprises an adjuvant to promote wetting and aid penetration of the wood by the aqueous solution, the adjuvant preferably comprising one or more of: a glycol, a hydrotrope, and a surfactant.
3. A method according to claim 2, wherein the surfactant is a non-ionic surfactant, preferably selected from alcohol ethyoxylate, alkyl polyglucoside, ethylene oxide-propylene oxide block copolymer, alkyl ethoxylate propoxylate, ethoxylated sorbitan monooleate, alkyl aryl alcohol ethoxylate 4. A method according to claim 2, wherein the hydrotrope is an aryl ethoxylate phosphate ester salt or an alkyl ethoxylate phosphate ester salt.5. A method according to any one of the preceding claims, wherein the film-forming polymer material is a styrene butadiene copolymer.6. A method according to any one of the preceding claims, wherein the second coating formulation further comprises an agent to promote keying of the -16 -polymer material into the surface of the wood the agent preferably being a glycol, particularly preferably butyl glycol.7. A method according to any one of the preceding claims, wherein the second coating formulation further comprises a crosslinking agent, preferably a zinc salt, to promote crosslinking of the polymer material.8. A method according to any one of the preceding claims, wherein the second coating formulation further comprises a UV-protecting agent, preferably titanium dioxide, to reduce UV damage of the polymer material.9. A method according to any one of the preceding claims, wherein the second coating formulation further comprises a material for increasing surface hydrophobicity, said material preferably being silicon dioxide.10. A method according to any one of the preceding claims, wherein the first coating formulation contains boric acid or borate ions in the range 48-72 g/L, ammonium or amine ions in the range 88-132 g/L and phosphate ions in the range 236-354 g/L.11. A method according to any one of the preceding claims, wherein the first coating formulation contains boric acid in the range 48-72 g/L and ammonium phosphate in the range 324 486 g/L.12. A method according to any one of the preceding claims, wherein step c) comprises applying the first coating formulation at a rate of 260±10 g/m2.13. A method according to any one of the preceding claims, wherein the film-forming polymer material makes up about 20-32%, preferably about 26%, of the second coating formulation by weight.14. A method according to any one of the preceding claims, wherein step e) -17 -comprises applying the second coating formulation at a rate of 100±10 g/m2.15. A method according to any one of the preceding claims, wherein the item of wood is a piece of timber which further comprises a second major surface opposed to the first major surface, the method further comprising: f) if the wood has a moisture content of greater than 20%, drying the wood so that it has a moisture content no greater than 20%; g) coating the second major surface with a first coating formulation comprising an aqueous solution containing boric acid or a salt thereof, an amine or 10 ammonium salt, and phosphate; h) repeating steps f) and g) and f); and then i) coating the second major surface with a second coating formulation comprising a film-forming polymer material in an aqueous carrier.16. An item of wood having at least a first major surface with fire retardant properties, wherein the first major surface is coated with a base coat containing boric acid or a salt thereof, an amine or ammonium salt, and phosphate, and with a top coat comprising a film of a polymer material, preferably a styrene butadiene copolymer.Amendments to the claims have been made as follows CLAIMS: 1. A method for improving fire retardant properties of an item of wood, the method comprising: a) providing an item of wood to be treated; b) if the wood has a moisture content of greater than 20%, drying the wood so that it has a moisture content no greater than 20%; c) coating a first major surface of the item of wood with a first coating formulation comprising an aqueous solution containing boric acid or a salt thereof, 10 an amine or ammonium salt, and phosphate; d) repeating steps b) and c) and b); and then e) coating the first major surface with a second coating formulation comprising a film-forming polymer material in an aqueous carrier.LC, 15 2. A method according to claim 1, wherein the first coating formulation further O comprises an adjuvant to promote wetting and aid penetration of the wood by the aqueous solution CNI 3. A method according to claim 2, wherein the adjuvant comprises one or more of: a glycol, a hydrotrope, and a surfactant.
4. A method according to claim 3, wherein the surfactant is a non-ionic surfactant.
5. A method according to claim 4, wherein the surfactant is selected from alcohol ethyoxylate, alkyl polyglucoside, ethylene oxide-propylene oxide block copolymer, alkyl ethoxylate propoxylate, ethoxylated sorbitan monooleate, alkyl aryl alcohol ethoxylate.
6. A method according to claim 3, wherein the hydrotrope is an aryl ethoxylate phosphate ester salt or an alkyl ethoxylate phosphate ester salt.
7. A method according to any one of the preceding claims, wherein the film-forming polymer material is a styrene butadiene copolymer.
8. A method according to any one of the preceding claims, wherein the second coating formulation further comprises an agent to promote keying of the polymer material into the surface of the wood.A method according to claim 8, wherein the agent is a glycol.10. A method according to claim 9, wherein the agent is butyl glycol.11. A method according to any one of the preceding claims, wherein the second coating formulation further comprises a crosslinking agent to promote LCD crosslinking of the polymer material. r 15o 12. A method according to claim 11, wherein the crosslinking agent is a zinc salt.C\I 13. A method according to any one of the preceding claims, wherein the second coating formulation further comprises a UV-protecting agent to reduce UV damage of the polymer material.14. A method according to claim 13, wherein the UV-protecting agent is titanium dioxide.15. A method according to any one of the preceding claims, wherein the second coating formulation further comprises a material for increasing surface hydrophobicity.16. A method according to claim 15, wherein the material for increasing surface hydrophobicity comprises silicon dioxide.17. A method according to any one of the preceding claims, wherein the first coating formulation contains boric acid or borate ions in the range 48-72 g/L, ammonium or amine ions in the range 88-132 g/L and phosphate ions in the range 236-354 g/L.18. A method according to any one of the preceding claims, wherein the first coating formulation contains boric acid in the range 48-72 g/L and ammonium phosphate in the range 324 486 g/L.19. A method according to any one of the preceding claims, wherein step c) comprises applying the first coating formulation at a rate of 260±10 g/m2.20. A method according to any one of the preceding claims, wherein the film- !" forming polymer material makes up about 20-32% of the second coating formulation by weight.21. A method according to claim 20, wherein the film-forming polymer material makes up about 26% of the second coating formulation by weight.22. A method according to any one of the preceding claims, wherein step e) comprises applying the second coating formulation at a rate of 100±10 g/m2.23. A method according to any one of the preceding claims, wherein the item of wood is a piece of timber which further comprises a second major surface opposed to the first major surface, the method further comprising: f) if the wood has a moisture content of greater than 20%, drying the wood so that it has a moisture content no greater than 20%; 9) coating the second major surface with a first coating formulation comprising an aqueous solution containing boric acid or a salt thereof, an amine or 30 ammonium salt, and phosphate; h) repeating steps f) and g) and f); and then i) coating the second major surface with a second coating formulation comprising a film-forming polymer material in an aqueous carrier. V) 0 CV