The invention relates to a fire blanket which is used typically to extinguish cooking oil fires. The conventional approach to extinguishing cooking oil fires (and like fires) is to use a fire blanket. Such fire blankets rely on the exclusion of oxygen to extinguish the fire. Such blankets must therefore be made of material which is, or is modified to be (such as by applying a suitable coating), capable of excluding oxygen during the high temperature condition in a fire. It may be difficult to provide suitable material in a sufficiently flexible form to enable effective deployment.
In a cooking oil fire, the burning of the oil can raise its temperature to more than that needed for auto-ignition. When a conventional fire blanket is used, therefore, the fire may re-strike if oxygen is allowed back into contact with the oil (after removal of the blanket).
In order to overcome these problems, it has been proposed to introduce chemically active extinguishing compounds into a fire blanket so that the fire blanket no longer relies entirely on the exclusion of oxygen to extinguish the fire.
United Kingdom Published Patent Application No. 2,359,020 (being the publication of the United Kingdom application corresponding to the above-mentioned parent U.S. application Ser. No. 10/202,697) discloses a fire blanket comprising two superimposed blanket layers (e.g. layers of a suitable fabric) which are stitched together with a suitable chemically active extinguishing compound held between the fabric layers, ready for deployment through the fabric onto the fire. More specifically, there is disclosed an arrangement in which the two blanket layers are stitched together to form a “quilted” configuration comprising a pattern of rectangular pockets or cells, each holding a quantity of the compound. Although such a blanket has been found to be very effective, it is less suitable for conditions where it may be subjected to elevated temperatures during transport or storage. Under such conditions, the chemical compound may soften into the form of a wet paste which then migrates into the fibres of the blanket fabric, rendering the blanket stiff and difficult or impossible to deploy subsequently. The present invention aims to overcome this problem.
Fire blankets are normally mounted in the risk area (such as a kitchen) by being folded up into a shallow box or container which is wall-mounted, the blanket being provided with pull tags attached to it by means of which the blanket can be rapidly pulled out of the container and then deployed on the fire. It is therefore desirable that it should be relatively easy to fold a blanket for insertion into the container or box, not only during the final stage of manufacture of the blanket but also after sale—such as after the blanket has been removed from its container for routine checking and inspection.
It can be difficult to fold the first-proposed blanket in order to match the shape of the mounting container or box into which it is to be inserted, because the blanket can in practice only be folded along the strips of material between the pockets or cells.
U.S. Pat. No. 5,032,446 (Sayles), issued Jul. 16, 1991, shows a fire blanket comprising two sheets of superimposed plastics material secured together so as to form a quilted configuration of an array of pockets, with each pocket containing a chemically active extinguishing agent. When deployed over a fire, the plastics material melts to release the chemical compound onto the fire. Here, the blanket being made only of plastics material, melts substantially immediately in the presence of the fire and there is effectively no oxygen-exclusion function. In addition, such a blanket is very difficult to fold and appears intended for semi-permanent mounting in flat form immediately adjacent to a fire risk area.
According to the invention, there is provided a fire blanket, comprising a fire blanket, comprising a flexible substrate, a chemical compound which reacts endothermically when heated and which melts when heated above a first predetermined temperature which is less than the temperature of a fire to be attacked by the blanket, bag means made of material which ruptures when heated above a second predetermined temperature which is higher than the first predetermined temperature and lower than the temperature of the fire to be attacked, the chemical compound being held in the bag means until the rupture thereof, the bag means being supported on and by the substrate, the substrate being configured to be porous to the melted chemical compound to allow the chemical compound to permeate therethrough towards and onto the fire after rupture of the bag means and melting of the chemical compound.
According to the invention, there is further provided a method of making a fire blanket, comprising the steps of laying out a first layer of blanket material, placing thereon in predetermined positions a plurality of sealed bags of predetermined size made of plastics material which rupture when heated at least to a first predetermined temperature which is lower than the temperature of a fire to be attacked by the blanket, each sealed bag containing a chemically active extinguishing compound which reacts endothermically when heated and which melts at a second predetermined temperature lower than the first predetermined temperature, placing a second blanket layer over the sealed bags on the first layer, and attaching the two blanket layers together along lines of attachment which pass between the sealed bags, some of the lines of attachment being spaced apart and extending in a first predetermined direction and the remainder thereof being spaced apart and extending in a second, transverse direction, whereby the lines of attachment cause the layers to form pockets in which are disposed the sealed bags, the blanket material being porous to the melted chemical compound to allow permeation of the melted chemical compound through the blanket material onto the fire after rupture of the sealed bags.
Fire blankets embodying the invention, and methods according to the invention of making fire blankets, will now be described, by way of example only, with reference to the accompanying diagrammatic drawings in which:
Cooking oil or fat fires are a common source of fire in the home. These fires are particularly dangerous because the burning of the liquid can raise its auto-ignition temperature to more than that needed for auto-ignition. Thus, cooking oil fires have a tendency to reignite or “restrike”. Furthermore, most conventional suppression agents such as water, CO2 foam or multipurpose dry chemicals, are ineffective against cooking oil fires.
The conventional approach to extinguishing cooking oil fires is therefore to use a fire blanket. Such fire blankets rely on the exclusion of oxygen to extinguish the fire. Often, due to the high temperatures involved (up to 360° C.), the blankets are made of woven glass fibres. Optionally, the blankets may be coated to improve exclusion of air.
Existing fire blankets have several problems. Where blankets are uncoated, the exclusion of oxygen relies entirely on the quality of the weave of the blanket. Any defects in the weave renders the blanket less effective in excluding oxygen and may allow oil vapour to escape above the blanket which may then ignite so that flame is presence above the blanket.
Where a coating is used, the blanket tends to become stiffer than a similar blanket without a coating. This reduces the effectiveness of the sealing of the blanket around the periphery of the pan containing the cooking oil fire which therefore reduces the effectiveness of oxygen exclusion. Also, the coating is usually in the form of silicon rubber which is sometimes flammable.
Even if it is possible to extinguish the fire, the burning of the oil may raise its temperature to above its auto-ignition temperature, as noted above, and therefore the fire may readily restrike if oxygen is allowed back into contact with the oil. This problem is exacerbated by the tendency for the oil to degrade during burning and thereby to have a reduced auto-ignition temperature. For example, the typical auto-ignition temperature of cooking oil (which is predominantly composed of fatty acid esters) is about 360° C. After burning, the auto-ignition temperature may become as low as 300° C.
In commercial restaurants, wet chemical agents are sometimes used instead of a fire blanket. These may be deployed either in fixed systems or in specially modified portable hand extinguishers. However, this approach is not suitable for use in the home where the simplicity and easy storage of a fire blanket is advantageous.
The solution proposed to overcome these problems is to introduce chemically active compounds into a fire blanket so that the fire blanket no longer relies entirely on the exclusion of oxygen to extinguish the fire.
Preferably, a wet or low melting temperature chemical agent such as an alkali metal salt, e.g. potassium or sodium acetate, lactate, citrate or carbonate is included in the fire blanket so that the fire blanket operates to exclude oxygen and also extinguishes the fire by chemical means. The chemically acting agent may be in the form of a low temperature melting solid or may be carried in suspension by a carrier solution such as by being in the form of an aqueous solution.
Dry chemical extinguishers have used alkali metal salts such as sodium bicarbonate for some time as described, for example, in Sheinson, RS “Fire Suppression by Fine Solid, Aerosol” proceedings of the International CFC and Halon Alternatives Conference, Washington, D.C., 24-26 Oct. 1994, pages 414-421.
In order to be effective both to exclude oxygen and for chemical suppression of a fire it will be understood that the chemical agent must approach the fire. Thus, the fabric substrate of a fire blanket, although of low permeability to air in order the exclude oxygen, should be configured to allow the melted or aqueous solution to pass through and so enter the fire to extinguish it by chemical means.
By incorporating alkali metal salts (typically sodium or potassium salts) into the blanket, advantage may be taken of the endothermic decomposition of these compounds when heated. Since the decomposition is endothermic, heat is taken out of the fire which improves cooling of the oil and therefore reduces the possibility of the fire restriking. Furthermore, the decomposition may release water which further cools the oil by evaporation. Similarly, any carrier solution may evaporate rather than drip through the blanket. Such evaporation of the carrier solution is generally a very endothermic (heat absorbing) process.
Additionally, if the salt solution is alkaline, the solution reacts chemically with the cooking oil to saponify the oil to produce a crust or lumps of generally inflammable “soap”. This further reduces the chance of re-ignition.
With reference to
The tests have been conducted using a 285 mm aluminium pan. In all other respects the tests followed the test protocol set out in British Standard—European Norm (BSEN) 1869:1997.
Test 1—Wet Blanket
Three litres of oil in a pan were heated to auto-ignition temperature (362° C.) and allowed to burn for two minutes. A pre-soaked blanket was then applied and the pan let to stand. As expected, fire extinction occurred instantly. Control was maintained for 15 minutes thereafter until the blanket was removed. After the blanket was removed, the fire reignited after approximately 20 seconds and so failed the BS 1869:1997 test. Thus, the wet blanket was shown to be inadequate as a fire blanket, not least because it did not reduce the temperature of the oil to below its auto-ignition temperature within a reasonable length of time.
Test 2—Blanket soaked in potassium acetate solutions
The test was conducted as in Test 1. A tea towel was soaked in a 40% aqueous solution of potassium acetate to form a fire blanket before being applied to the pan. The fire was extinguished immediately and remained under control for 15 minutes. After removal at the 15 minute point, the fire did not restrike for at least 3 minutes. This constituted a pass to British/European Standard (BSEN) 1869:1997.
At the end of the test, the towel was slightly charred (but less than in Test 1). It is believed that the high concentration of potassium salts prevented the fire from causing as much damage to the underlying tea towel material.
Test 3—Blanket soaked in potassium acetate solution and then additional potassium acetate solution added after fire suppression
This test was carried out as for Test 2 but additional 40% aqueous solution of potassium acetate was periodically applied to the top of the blanket during the 15 minute control hold time after extinguishing the fire. This was expected to produce additional cooling by evaporation of the water and also more effective saponification of the oil due to the additional quantities of potassium acetate solution. During the additional application of potassium acetate solution, hissing and boiling occurred due to the flash evaporation of the aqueous solution.
The addition of about 150 ml of aqueous potassium acetate solution resulted in a much higher degree of cooling as shown in
Test 4—Sodium Acetate Trihydrate
Sodium acetate trihydrate has a melting point of about 58° C. and thus may be applied to the blanket or secured therein in solid form. During extinguishing, the compound melts and drops into the oil. This test was conducted as with the above tests and the fire was held extinguished for 15 minutes and did not reignite for at least 3 minutes after removal.
An examination of
Thus the tests show that improved extinguishing can be achieved using a “chemically active” fire blanket. The chemically active component is typically an alkali metal salt and preferably a potassium or sodium salt. Preferably, to cause saponification, the solution produced by the compound is alkaline.
Blankets embodying the present invention will now be described in detail, with particular reference to
The blanket comprises two layers 10,12 (see
During manufacture, one blanket layer 12 is placed on a flat surface. Individual “bags”, to be described in detail below, are then placed on the lower blanket layer 12 in a rectangular array of rows and columns as shown in
An enlarged diagrammatic cross-section through one of the bags 14 is shown in
After the bags have been positioned on the lower blanket layer 12, as shown in
The blanket is provided with “handles” 20,22, in the form of fabric strips securely stitched adjacent to one edge of the blanket.
The blanket is normally held in a shallow container or box. The box will be described in more detail with reference to
As already explained, the blanket provides an initial and continuing fire extinguishing action by excluding oxygen from the fire. In addition, however, the heat of the fire melts the extinguishant compound in the bags 14 and causes the plastics material of the bags to melt or burst. The chemical compound thus permeates through the material of the fabric (such as through the weave if the blanket is made of woven material), via a combination of capillary action and gravity. The fabric of the blanket is arranged and selected so that its original structural integrity remains intact without breakage or rupture so as to enable the released chemical compound to permeate through it. Such structural integrity also ensures that a good barrier is presented and continuously presented to stop air or oxygen reaching the hot oil fire.
The extinguishant compound 16 incorporated in the bag 14 will normally melt or liquify at about 60° C., such as in the case of sodium acetate trihydrate (and similar melting or liquifying temperatures apply to the other extinguishants mentioned). The plastics material 15A, 15B of the bags 14 melts at about 120° C. Therefore, even if the blanket should be subjected to temperatures of the order of 60° C. during transport or storage, thus causing the extinguishant compound to melt or liquify, the extinguishant compound will still be securely retained within the bags 14. The extinguishant is therefore ready for release in the manner already indicated when the blanket is deployed over a fire and the plastics material of the bag 14 rises above 120° C. and melts. In this way, the problem mentioned above, of premature release of the extinguishant compound into the blanket fabric layers when subjected to elevated temperatures during transport or storage, is completely overcome, and the risk of such release causing the blanket to become stiff and effectively unusable is therefore avoided.
It will be clear that many modifications may be made. For example, the bags 14 can be larger or smaller in relation to the size of the pockets or cells of the blanket in which they are situated. The bags 14 need not be square or rectangular in configuration but could instead be circular, for example. A particularly advantageous shape is triangular because bags of this shape can be packed very efficiently together in the blanket to give a high density of the chemical compound if required. The stitching in the blanket could be arranged to provide pockets of triangular shape as well.
It may be advantageous for the size of the bags 14 to vary over the region E, so that the bags 14 closest to the centre of this region E contain more of the extinguishant compound than those further away from the centre. In this way, the extinguishing action performed by the extinguishant compound is concentrated in the centre of the blanket, where the fire may be fiercest. The sizes of the pockets can be varied as required—such as being made smaller to increase the density of the chemical compound (for bags of a particular size).
The edge regions A,B,C and D of the blanket can be larger or smaller than shown. They may be devoid of the stitching.
If the material of the blanket layers is suitable, then the pockets or cells could be formed not by stitching along the lines 17,18 but by some other suitable process such as adhesive or welding.
The fabric material of the blanket is advantageously treated with a fire retardant. The thread used to stitch the blanket also needs to be able to withstand high temperature. Suitable material is Kevlar (Trade Mark).
As stated, the blanket is placed in the container 24 in a folded configuration. A feature of the blanket being described facilitates such folding. Ease of folding is clearly advantageous for use during the final stage of manufacture. It is also a desired feature after sale of the blanket. Thus, the blanket may need to be removed from the container 24 in a non-emergency situation, for inspection or training purposes. In such cases, it is necessary of course to re-fold the blanket for insertion back into the container.
In order to facilitate such folding of the blanket, in particular regions on the blanket (see
As shown in
It will be observed that the two blankets according to the invention, producing plots I and III, cause the temperature of the oil to be reduced significantly more rapidly than does the conventional blanket (plot II).
At time=17 minutes, the blanket under test is removed. At this time, it was observed that the conventional blanket (plot II) had reduced the oil temperature to 330° C. This temperature is still above the auto-ignition temperature of the oil, and it was observed that the fire was re-struck. Thus, this blanket failed the test under BS 1869:1997. However, at time=17 minutes, the blankets according to the invention had reduced the oil temperature significantly more (to less than 310° C. in the case of plot I and to slightly above this temperature in the case of plot III). The oil temperature is less than its auto-ignition temperature, and removal of the blanket does not cause the fire to re-strike.
It is important that the fire blanket creates an air-tight barrier to starve the fire of oxygen. Thus, the underlying fabric must be able to remain wetted by the melt or solution in order to provide the air barrier once the chemically active component has dripped through onto the seat of the fire. Clearly, in such circumstances, it is necessary to select the fabric carefully in terms of its weight (gsm), its weave and the fibre denier etc. Typically the fabric will retain some of the melted chemically active component by surface tension and thus seal holes in the weave and so create at least a partially air-tight barrier to starve the fire of oxygen. Although a woven cloth is preferred, it will be understood that in some situations a non-woven felt may be used. The fabric weave density is the key to maintaining air exclusion.
A typical fabric will have a simple 1×1 weave with a 50% cotton/50% polyester thread. A suitable fabric is made by Copland Fabric, Burlington, N.C. 27216 under their style code 10015/1. However, it will be understood that tea towel or bed sheet type materials may be used and, rather than a simple weave, cross woven or bow weave materials could be used. Typically, in the fabric the thread, both in weft and warp, will be about 35/1 denier and there will be around 45 to 50 threads per inch. However, 50 threads per inch is preferred in order to provide a fabric which is tight enough to retain the chemically active agent when stored but sufficiently open to allow the agent to drip through to a fire when melted.
The primary means of fire extinguishing by a fire blanket is by limiting oxygen. However, inclusion of chemically active agents such as sodium acetate trihydrate enhances fire extinguishing action by removing heat and also by reducing fuel (oil) temperatures which also inhibits restrike when the blanket is removed and oxygen is available. The use of the plastic bags 14, for holding the extinguishant, enables the fabric to maintain the oxygen limiting feature whilst acting as a matrix to store, present and distribute the chemically active agent to reduce temperatures. Thus, the specific choice of fabric, the material of the bags 14 and the chemically active agent will depend upon requirements, storage conditions, cost etc.
As alternatives to sodium acetate trihydrate, it may be possible where conditions allow, to use potassium acetate or potassium citrate as the chemically active agent.
Number | Date | Country | Kind |
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0003349.8 | Feb 2000 | GB | national |
0100529.7 | Jan 2001 | GB | national |
This application is a continuation-in-part of Application Ser. No. 10/203,697, filed Nov. 8, 2002, which is a 371 of PCT/GB01/00575, filed Feb. 9, 2001, which claims benefit of Great Britain application 0003349.8, filed Feb. 14, 2000, and Great Britain application 0100529.7, filed Jan. 9, 2001.
Number | Date | Country | |
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Parent | 10203697 | Nov 2002 | US |
Child | 10894959 | Jul 2004 | US |