This is a National Phase Application in the United States of International Patent Application No. PCT/JP2014/000765 filed Feb. 14, 2014, the entire disclosure of which is hereby incorporated by reference.
The invention relates to a heat-absorbing material using a magnesium phosphate hydrate and a producing method thereof.
It is required for some facilities such as atomic power plants and thermal power plants that cables in the facilities have heat resistance or fire resistance against extraordinary accidents, e.g., fire. The heat resistance or fire resistance of cables is usually realized by covering the cables with a heat-absorbing material.
Conventional heat-absorbing materials include a water-containing polymer absorber and aluminum hydroxide hydrate. When heated, the polymer absorber absorbs heat, and the aluminum hydroxide hydrate absorbs heat by using water molecules (crystal water) contained therein.
However, the conventional heat-absorbing materials are bulky and heavy. Thus it is difficult to replace the covering of cables after laying cables since a working area for the exchange is narrow.
The polymer absorber is usually packed. If the package is broken, water evaporates at room temperature so that the polymer absorber becomes unable to function.
The absorber using aluminum hydroxide hydrate has a defect that cables are damaged before the hydrate decomposes since the decomposition temperature of hydrate is higher than the heatproof temperature of cables.
From the above, a heat-absorbing material is needed which does not require exchange, can be arranged in a small place, is lightweight and can efficiently absorb heat.
Magnesium phosphate hydrates are known as a heat-absorbing material (Patent Documents 1 and 2).
Patent Document 1: JP-A-2008-274253
Patent Document 2: JP-A-2009-191493
An object of the invention is to provide a novel heat-absorbing material.
As a result of diligent research, the inventors have found that a heat-absorbing material using particles containing a magnesium phosphate hydrate is easy to be handled and excellent as a heat-absorbing material, and made the invention based on the finding.
According to the invention, the following heat-absorbing material and production method therefor are provided.
According to the invention, it is possible to provide a novel heat-absorbing material.
The heat-absorbing material of the invention comprises particles that comprise a magnesium phosphate hydrate and a binder.
Magnesium phosphate hydrates include magnesium phosphate tribasic octahydrate (Mg3(PO4)2.8H2O) and 3, 5, 10 and 22 hydrates thereof. Magnesium phosphate tribasic octahydrate is preferred. Magnesium phosphate tribasic octahydrate decomposes and absorbs heat from around 100° C.
Inorganic binders and organic binders can be used as a binder.
Inorganic binders include sodium silicate (liquid glass derivatives, Na2SiO3, Na2O.SiO2 or Na2O.nSiO2.mH2O), colloidal silica and bentonite. Sodium silicate is preferred.
Organic binders include PVA (polyvinylalcohol), CMC (carboxylmethylcellulose) and starch.
The heat-absorbing material of the invention may consist of a magnesium phosphate hydrate and a binder, excluding inevitable impurities.
The particles contain generally 1 to 99 wt % of magnesium phosphate hydrate and 1 to 99 wt % of binder, preferably 50 to 99 wt % of magnesium phosphate hydrate and 1 to 50 wt % of binder, more preferably 70 to 99 wt % of magnesium phosphate hydrate and 1 to 30 wt % of binder.
The invention uses granulated heat-absorbing material. If the heat-absorbing material is used in a state of powder, it is difficult to put the powder into a bag (e.g., difficult to seal the bag) and powder tends to be non-uniformly filled mainly in the bottom of the bag. The average diameter of the particles is preferably 0.01 mm to 20 mm, more preferably 0.1 mm to 15 mm. As the diameter decreases, the surface area increases, so that these become excellent as a heat-absorbing material but difficult to be handled.
The heat-absorbing material of the invention is usually used as being put in a container such as a bag and a case. It is preferred that the heat-absorbing material be put into a bag made of a heat-resistant cloth such as fabric, sheet and film and the bag be closed. Heat-resistant cloths include a glass cloth, a silica cloth and an alumina cloth. A cloth on the surface of which aluminum is deposited is excellent in heat resistance. The container is not required to be airtight.
The particles used for the heat-absorbing material can be obtained by mixing a magnesium phosphate hydrate and a liquid glass (Na2O.nSiO2.mH2O) to form a mixture, granulating the mixture to form hydrous particles, and removing water from the hydrous particles. If necessary, the particles thus obtained are put into a container.
The heat-absorbing material of the invention can be solely used as a heat-insulator. The heat-absorbing material may be used together with other insulators to form more effective insulate structure exhibiting strong insulation and fire resistance.
Magnesium phosphate tribasic octahydrate and liquid glass No. 3 (sodium silicate) (Na2O.nSiO2.mH2O (n=3.0 to 3.4)) were mixed in a weight ratio of 91:9 and granulated to obtain hydrous particles with an average diameter of 2 mm to 7 mm. The water contained in the hydrous particles was removed by drying at 90° C. to obtain particles. The particles thus obtained were accommodated in bags made from glass cloth, thereby producing a heat-absorbing material. The shape of bags was a 160 mm×160 mm rectangle and the bags were connected in series with gussets having a width of 10 mm therebetween as shown in
A refractory structure shown in
As shown in
As shown in
The cable rack 100 was placed in a vertical furnace.
First insulator: composite of aerogel and inorganic fiber (Pyrogel, Aspen Inc.)
Second insulator: bio-soluble fiber blanket (Composition of bio-soluble fiber: SiO2 content, about 73 mass %; CaO content, about 25 mass %; MgO content, about 0.3 mass %; and Al2O3 content, about 2 mass %)
Thermocouples were placed between the second layer and the third layer from the inside of the second insulator 24 (48 in
In the vertical furnace, heating was conducted by a burner for 3 hours according to ISO standard fireproof curve, thereafter cooling by standing for 2 hours. Table 1 shows temperatures (° C.) measured after 1, 2, 3, 5, 8 and 10 hours at the positions of thermocouples.
As shown in Table 1, even when the temperature of the outside exceeded 1000° C., the temperature just above the cable case 40 was about 163° C., thereby confirming continuity of cables. The temperature just above the cable case 40 was maintained to be 100° C. for about 20 minutes after about 3 hours lapsed from the start of heating, which appears to be caused by evaporation of water contained in the heat-absorbing material.
The heat-absorbing material of the invention can be used as a heat-absorbing material in places and equipment such as atomic power plants for which fire resistance is required.
Although only some exemplary embodiments and/or examples of this invention have been described in detail above, those skilled in the art will readily appreciate that many modifications are possible in the exemplary embodiments and/or examples without materially departing from the novel teachings and advantages of this invention. Accordingly, all such modifications are intended to be included within the scope of this invention.
The documents described in the description is incorporated herein by reference in its entirety.
Filing Document | Filing Date | Country | Kind |
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PCT/JP2014/000765 | 2/14/2014 | WO | 00 |
Publishing Document | Publishing Date | Country | Kind |
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WO2015/121894 | 8/20/2015 | WO | A |
Number | Name | Date | Kind |
---|---|---|---|
20040203310 | Watanabe | Oct 2004 | A1 |
20080132594 | Iwase | Jun 2008 | A1 |
20100108434 | Iwase | May 2010 | A1 |
20130034732 | Parker | Feb 2013 | A1 |
20170297298 | Tsumura | Oct 2017 | A1 |
Number | Date | Country |
---|---|---|
9-3778 | Jan 1997 | JP |
2006-160858 | Jun 2006 | JP |
2008-138032 | Jun 2006 | JP |
2008-274253 | Nov 2008 | JP |
2009-191493 | Aug 2009 | JP |
2010-126389 | Jun 2010 | JP |
2010-126961 | Jun 2010 | JP |
Entry |
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Extended European Search Report issued in corresponding application 14882256.2 completed Sep. 7, 2017 and dated Sep. 18, 2017. |
International Search Report issued in corresponding application PCT/JP2014/000765, completed Mar. 11, 2014 and dated Mar. 18, 2014. |
International Preliminary Report on Patentability issued in corresponding application PCT/JP2014/000765 dated Aug. 16, 2016. |
Number | Date | Country | |
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20170009139 A1 | Jan 2017 | US |