SYNTACTIC FOAM

20180155519 ยท 2018-06-07

    Inventors

    Cpc classification

    International classification

    Abstract

    A fire resistant syntactic foam material, the material comprising the reaction product of a reaction mixture including a resole cold curing phenolic resin and incorporating a plurality of hollow spheres, the reaction mixture also including a solution of a partial phosphate ester, a low viscosity phosphate plasticiser, a reinforcing filler and a particulate filler.

    Claims

    1. A fire resistant syntactic foam material, the material comprising the reaction product of a reaction mixture including a resole cold curing phenolic resin and incorporating a plurality of hollow spheres, the reaction mixture also including a solution of a partial phosphate ester, a low viscosity phosphate plasticiser, a reinforcing filler and a particulate filler, characterised in that the particulate filler is any of cork, graphite or vermiculite.

    2. A fire resistant foam material according to claim 1, characterised in that the low viscosity phosphate plasticiser is present in an amount up to 8.5% by weight of the phenolic resin.

    3. (canceled)

    4. A fire resistant foam material according to claims 1, characterised in that the proportion by weight of the partial phosphate ester to the phenolic resin in the reaction mixture is in the range of 5% to 15%.

    5-6. (canceled)

    7. A fire resistant foam material according to claims 1, characterised in that the hollow spheres are present in a concentration in the range of plus or minus 15% of the volume concentration.

    8. A fire resistant foam material according to claims 1, characterised in that the reaction mixture includes sulphonic acid.

    9. A fire resistant foam material according to claim 8, characterised in that the amount of sulphonic acid in the reaction mixture is up to 6% of the weight of the partial phosphate ester.

    10. A fire resistant foam material according to claims 1, characterised in that the reaction mixture includes trifluoromethanesulfonic acid in an amount up to 6% of the weight of the partial phosphate ester.

    11. A fire resistant foam material according to claims 1, characterised in that the concentration of the hollow spheres is such that the effective specific gravity of the material is between 0.2 and 0.6.

    12. A fire resistant foam material according to claims 1, characterised in that the hollow spheres are formed from a material selected from glass, thermoplastic copolymers of polyacrylonitrile, a refractory material, or a ceramic material.

    13. A fire resistant foam material according to claims 1, characterised in that the reinforcing filler is selected from basalt fibres, ceramic fibres, glass fibres and glass flake.

    14. A fire resistant foam material according to claims 1, characterised in that the reaction mixture includes a surfactant.

    15. A fire resistant foam material according to claim 14, characterised in that the surfactant is a fluorinated surfactant.

    16. A fire resistant foam material according to claim 14 or 15, characterised in that the surfactant is acid resistant.

    17. A fire resistant foam material according to claims 1, characterised in that the reaction mixture includes an accelerator.

    18. A fire resistant foam material according to claim 17, characterised in that the accelerator is para-toluene sulfonic acid.

    19. A two-part system for the production of a fire resistant syntactic foam material, the system comprising a first reactant including a resole cold curing phenolic resin and a second reactant, one or both of which reactants incorporate a plurality of hollow spheres, the second reactant comprising a partial phosphate ester, the spheres being incorporated in one or both of the reactants and the system also incorporating a low viscosity phosphate plasticiser, a reinforcing filler and a particulate filler, characterised in that the particulate filler is any of cork, graphite or vermiculite.

    20-21. (canceled)

    22. A two-part system according to claim 19, characterised in that the particulate filler is incorporated in the first reactant.

    23-28. (canceled)

    29. A two-part system according to claim 19, characterised in that the reinforcing filler is incorporated in the first reactant.

    30-32. (canceled)

    33. A method of producing a fire resistant syntactic foam material comprising mixing a resole cold curing phenolic resin incorporating hollow spheres with a further constituent and allowing the mixture to cure at ambient temperature, with the further constituent comprising a solution of a partial phosphate ester, a low viscosity phosphate plasticiser, a reinforcing filler, and a particulate filler, characterised in that the particulate filler is any of cork, graphite or vermiculite.

    34-46. (canceled)

    47. A fire resistant component or structure, the surface thereof being coated with a fire resistant syntactic foam material according to any of the preceding claims 1.

    48-60. (canceled)

    Description

    EXAMPLES

    [0057] Examples 1 to 4 below are typical formulations according to the invention.

    TABLE-US-00001 Example Example Example Example 1 2 3 4 First Part Resole cold curing phenolic 60.05 60.05 62.5 63 resin Phosphate Plasticiser 5.1 5.1 3 5 Silane Adhesion Promoter 0.67 0.67 0.55 0.7 Surfactant 0.30 0.3 0.3 0.35 Glass fibres 1.51 0 0 1.75 Basalt fibres 0 1.51 2 1 Ceramic Fibres 1.51 1.51 1 1.5 Thermoplastic Spheres 3.44 3.44 0 0 Hollow glass spheres 10.85 10.85 14.27 14.41 3 mm Cork Granules 8.24 8.24 0 0 Vermiculite 0 0 8.2 0 Graphite 0 0 0 2 Second Part Para-toluene sulphonic acid 0.42 0.42 0.45 0.5 Partial Phosphate Ester 7.49 7.69 7.34 9.49 Trifluromethanesulphonic 0.42 0.22 0.39 0.3 acid

    [0058] Regarding example 1 above, the specific gravity of the cured material is 0.35.

    [0059] After mixing the first and second parts as per step 3 of the manufacturing process described above, the mixture is cast and cured at ambient temperature. The resulting fire resistant syntactic foam material was used to prepare a fire resistant enclosure (10) and subjected to a two hour jet fire test according to ISO 22899-1. The maximum temperature observed was 145.5 C. (Maximum temperature rise allowable is 400 C.).

    [0060] The material of the enclosure (10) was made up of three layers as shown in FIG. 1. The inner layer (12) is a 2 mm thick phenolic laminate system. The outer layer (14) is a 3 mm thick phenolic laminate system, and the internal layer (16) is the syntactic foam material of example 1. The thickness of the internal layer is a 50 mm.

    [0061] The main components of the examples of the present invention provide at least the following functions.

    [0062] (1) Phenolic resins. The cold curing resins are resoles. For the purposes of the present application the lowest possible viscosity resin used is typically below 500 c.poise.

    [0063] (2) Phosphate plasticiser. The viscosity of the mixture of the uncured syntactic foam is adjusted with up to 8.5% of the weight of the phenolic resin with a phosphate triester plasticiser. Any low viscosity phosphate plasticiser may be used such as di methyl methyl phosphonate, or Trichloroethyl phosphate.

    [0064] (3) Surfactant. The incorporation of the hollow spheres into the phenolic resins is improved by the addition of a fluorinated surfactant. The efficacy of the formulation both in terms of cohesion and adhesion and the ease of incorporation and of flow is greatly aided by the presence of suitable surfactants. These must be both temperature and acid stable and soluble in aqueous media.

    [0065] (4) Hollow glass spheres. As the effectiveness of the product in terms of thermal conductivity depends on providing a low thermal conductivity path through the foam then the lightest hollow glass sphere, consistent with durability in mixing and application is satisfactory. That the sphere shatters when exposed to stress or stain is irrelevant with respect to the prevention of incipient cracks, which depends only on the sphere diameter. Further, the careful adjustment of the resin viscosity, the incorporation of suitable wetting agents and the control of the mixer speed are necessary to prevent the rupture of the very light filler incorporated in this invention. Typically the preferred sphere will expanded from borosillicate glass with an effective specific gravity of 0.15-0.35 and have a mean particle diameter of 30-200 microns.

    [0066] Within the prescribed materials the effective specific gravity of the foam is adjusted by varying the rate of addition of the hollow glass spheres to between 0.30 and 0.6. The examples provided utilise hollow spheres composed of glass, although hollow spheres composed of refractory or ceramic materials would be equally efficacious.

    [0067] (5) Conventionally, the acid curing agents used with cold curing phenolic resins have been partially neutralised phosphoric acid. Esters of ortho and higher condensed phosphoric acids suitably accelerated with other acids such as para-toluene sulphonic acids give a slower more thorough cure to the cold curing resins specified herein.

    [0068] Further, because the acid value of the partial phosphate esters is lower than for the neutralised phosphoric acids but the pKa value of the residual oxyphosphorous functionality is similar a greater quantity of such partial phosphate ester curing agent is required to react with the methalol functionality of the resin. In the present application the greater quantity of curing agent added is critical in reducing the mix viscosity to allow the paste to both flow and be sprayed.

    [0069] The quantity of partial phosphate ester required to cure the phenolic resin is dependent on the methalol functionality of the phenolic resin. This functionality defines a concentration of partial phosphate ester of between 5 and 15% of partial phosphate ester calculated on the solids of both the partial phosphate ester and the phenolic resin.

    [0070] (6) Accelerators. The cure rate of the curing system is controlled by the addition of para-toluene sulphonic acid or triflouromethanesulfonic acid of up to 5% of the weight of the partial phosphate ester.

    [0071] (7) Reinforcing filler. Additionally the strength of the foam under fire conditions is advantageously modified by the addition of reinforcing fillers such as basalt fibres, ceramic fibres, glass fibres or glass flake. These materials control the mode of thermal decomposition of the structure and can reduce cracking. Reinforcing fillers therefore provide a material with enhanced durability.

    [0072] (8) Particulate filler. The composition also includes discrete particles in the form of particulate fillers. Examples of suitable particulate fillers include cork, graphite and vermiculite. Particulate fillers improve the integrity of the syntactic foam material during a fire regime and improve the physical properties of the syntactic foam material.

    [0073] Particulate fillers substantially prevent the syntactic foam material explosively decomposing during a fire regime, which would otherwise lead to a reduction or complete loss of the ability of the material to resist fire and intense heat and to provide thermal insulation. This phenomenon occurs in closed cell insulation materials at or above the temperature at which steam forms, leading to back pressure building within the material which back pressure causes the material to explode.

    [0074] Particulate fillers also reduce shrinkage and crack formation of the syntactic foam material and allow for out-gassing during a fire regime. Graphite, for instance, expands when heated reducing shrinkage of the syntactic foam material during a fire regime.

    [0075] There is thus described a fire resistant syntactic foam material with a number of advantages. As indicated above the addition of a particulate filler to the material provides a material with an improved performance by being resistant to explosive decomposition, shrinkage and cracking during a fire regime.

    [0076] Although embodiments of the present invention have been described in the preceding paragraphs with reference to various examples, it should be appreciated that modifications to the examples given can be made without departing from the scope of the invention as claimed. For example, different materials or different proportions of materials may be used.

    [0077] Features described in the preceding description may be used in combinations other than the combinations explicitly described.

    [0078] Although functions have been described with reference to certain features, those functions may be performable by other features whether described or not.

    [0079] Although features have been described with reference to certain embodiments, those features may also be present in other embodiments whether described or not.

    [0080] Whilst endeavoring in the foregoing specification to draw attention to those features of the invention believed to be of particular importance it should be understood that the Applicant claims protection in respect of any patentable feature or combination of features hereinbefore referred to and/or shown in the drawings whether or not particular emphasis has been placed thereon.