AU2012202891A1 - Method for extinguishing coal mine fires and unit for performing said method - Google Patents
Method for extinguishing coal mine fires and unit for performing said method Download PDFInfo
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- AU2012202891A1 AU2012202891A1 AU2012202891A AU2012202891A AU2012202891A1 AU 2012202891 A1 AU2012202891 A1 AU 2012202891A1 AU 2012202891 A AU2012202891 A AU 2012202891A AU 2012202891 A AU2012202891 A AU 2012202891A AU 2012202891 A1 AU2012202891 A1 AU 2012202891A1
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- water
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- extinguishing
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- 239000003245 coal Substances 0.000 title abstract description 25
- 238000000034 method Methods 0.000 title abstract description 16
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 abstract description 38
- 229920001577 copolymer Polymers 0.000 abstract description 16
- 230000008961 swelling Effects 0.000 abstract description 12
- 229920000642 polymer Polymers 0.000 description 17
- 238000002347 injection Methods 0.000 description 10
- 239000007924 injection Substances 0.000 description 10
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 7
- 238000002485 combustion reaction Methods 0.000 description 7
- 239000000499 gel Substances 0.000 description 7
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 6
- HRPVXLWXLXDGHG-UHFFFAOYSA-N Acrylamide Chemical compound NC(=O)C=C HRPVXLWXLXDGHG-UHFFFAOYSA-N 0.000 description 5
- 239000003431 cross linking reagent Substances 0.000 description 5
- 239000006260 foam Substances 0.000 description 5
- 230000002269 spontaneous effect Effects 0.000 description 5
- 238000001033 granulometry Methods 0.000 description 4
- 238000009434 installation Methods 0.000 description 4
- 150000003839 salts Chemical class 0.000 description 4
- 241000269793 Cryothenia peninsulae Species 0.000 description 3
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 3
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 3
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 238000005516 engineering process Methods 0.000 description 3
- 239000012530 fluid Substances 0.000 description 3
- 238000004519 manufacturing process Methods 0.000 description 3
- 238000002156 mixing Methods 0.000 description 3
- 239000000203 mixture Substances 0.000 description 3
- ZIUHHBKFKCYYJD-UHFFFAOYSA-N n,n'-methylenebisacrylamide Chemical compound C=CC(=O)NCNC(=O)C=C ZIUHHBKFKCYYJD-UHFFFAOYSA-N 0.000 description 3
- 239000001301 oxygen Substances 0.000 description 3
- 229910052760 oxygen Inorganic materials 0.000 description 3
- -1 poly(ethylene oxide) Polymers 0.000 description 3
- 238000007789 sealing Methods 0.000 description 3
- MYRTYDVEIRVNKP-UHFFFAOYSA-N 1,2-Divinylbenzene Chemical compound C=CC1=CC=CC=C1C=C MYRTYDVEIRVNKP-UHFFFAOYSA-N 0.000 description 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- 229920002134 Carboxymethyl cellulose Polymers 0.000 description 2
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 2
- WHNWPMSKXPGLAX-UHFFFAOYSA-N N-Vinyl-2-pyrrolidone Chemical compound C=CN1CCCC1=O WHNWPMSKXPGLAX-UHFFFAOYSA-N 0.000 description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 2
- 125000000746 allylic group Chemical group 0.000 description 2
- 239000000440 bentonite Substances 0.000 description 2
- 229910000278 bentonite Inorganic materials 0.000 description 2
- SVPXDRXYRYOSEX-UHFFFAOYSA-N bentoquatam Chemical compound O.O=[Si]=O.O=[Al]O[Al]=O SVPXDRXYRYOSEX-UHFFFAOYSA-N 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- 239000004202 carbamide Substances 0.000 description 2
- 239000001768 carboxy methyl cellulose Substances 0.000 description 2
- 235000010948 carboxy methyl cellulose Nutrition 0.000 description 2
- 239000008112 carboxymethyl-cellulose Substances 0.000 description 2
- 238000001816 cooling Methods 0.000 description 2
- 239000007789 gas Substances 0.000 description 2
- 229910052739 hydrogen Inorganic materials 0.000 description 2
- 239000011261 inert gas Substances 0.000 description 2
- 229910052500 inorganic mineral Inorganic materials 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 229910052751 metal Inorganic materials 0.000 description 2
- 239000002184 metal Substances 0.000 description 2
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 2
- 239000011707 mineral Substances 0.000 description 2
- 235000010755 mineral Nutrition 0.000 description 2
- 238000005065 mining Methods 0.000 description 2
- 239000000178 monomer Substances 0.000 description 2
- 229920002401 polyacrylamide Polymers 0.000 description 2
- 238000006116 polymerization reaction Methods 0.000 description 2
- 239000011780 sodium chloride Substances 0.000 description 2
- 159000000000 sodium salts Chemical class 0.000 description 2
- 239000002689 soil Substances 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 229920001897 terpolymer Polymers 0.000 description 2
- 229920001285 xanthan gum Polymers 0.000 description 2
- OBRHFMNBWAWJRM-UHFFFAOYSA-N (prop-2-enoylamino) 2-methylpropane-2-sulfonate Chemical compound CC(C)(C)S(=O)(=O)ONC(=O)C=C OBRHFMNBWAWJRM-UHFFFAOYSA-N 0.000 description 1
- GJCOSYZMQJWQCA-UHFFFAOYSA-N 9H-xanthene Chemical compound C1=CC=C2CC3=CC=CC=C3OC2=C1 GJCOSYZMQJWQCA-UHFFFAOYSA-N 0.000 description 1
- 239000005995 Aluminium silicate Substances 0.000 description 1
- 239000004254 Ammonium phosphate Substances 0.000 description 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
- KRKNYBCHXYNGOX-UHFFFAOYSA-K Citrate Chemical compound [O-]C(=O)CC(O)(CC([O-])=O)C([O-])=O KRKNYBCHXYNGOX-UHFFFAOYSA-K 0.000 description 1
- 244000007835 Cyamopsis tetragonoloba Species 0.000 description 1
- 229920002307 Dextran Polymers 0.000 description 1
- MYMOFIZGZYHOMD-UHFFFAOYSA-N Dioxygen Chemical compound O=O MYMOFIZGZYHOMD-UHFFFAOYSA-N 0.000 description 1
- 229920003171 Poly (ethylene oxide) Polymers 0.000 description 1
- 239000004372 Polyvinyl alcohol Substances 0.000 description 1
- 229920002125 Sokalan® Polymers 0.000 description 1
- 229910000831 Steel Inorganic materials 0.000 description 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 150000003926 acrylamides Chemical class 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 230000000996 additive effect Effects 0.000 description 1
- 229920000615 alginic acid Polymers 0.000 description 1
- 235000010443 alginic acid Nutrition 0.000 description 1
- 229910052783 alkali metal Chemical class 0.000 description 1
- 150000001340 alkali metals Chemical class 0.000 description 1
- 229910052784 alkaline earth metal Inorganic materials 0.000 description 1
- 150000001342 alkaline earth metals Chemical class 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- 235000012211 aluminium silicate Nutrition 0.000 description 1
- ZRIUUUJAJJNDSS-UHFFFAOYSA-N ammonium phosphates Chemical class [NH4+].[NH4+].[NH4+].[O-]P([O-])([O-])=O ZRIUUUJAJJNDSS-UHFFFAOYSA-N 0.000 description 1
- 235000019289 ammonium phosphates Nutrition 0.000 description 1
- 239000012736 aqueous medium Substances 0.000 description 1
- 239000011230 binding agent Substances 0.000 description 1
- 239000002981 blocking agent Substances 0.000 description 1
- 230000000903 blocking effect Effects 0.000 description 1
- 239000011449 brick Substances 0.000 description 1
- 229910052791 calcium Inorganic materials 0.000 description 1
- 235000013877 carbamide Nutrition 0.000 description 1
- 239000004568 cement Substances 0.000 description 1
- 239000004927 clay Substances 0.000 description 1
- 238000004939 coking Methods 0.000 description 1
- 239000002131 composite material Substances 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 229920006037 cross link polymer Polymers 0.000 description 1
- 238000004132 cross linking Methods 0.000 description 1
- 229920006035 cross-linked graft co-polymer Polymers 0.000 description 1
- 230000003247 decreasing effect Effects 0.000 description 1
- 229910001882 dioxygen Inorganic materials 0.000 description 1
- 239000012153 distilled water Substances 0.000 description 1
- 239000003651 drinking water Substances 0.000 description 1
- 235000020188 drinking water Nutrition 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 238000004880 explosion Methods 0.000 description 1
- 238000004079 fireproofing Methods 0.000 description 1
- 239000010881 fly ash Substances 0.000 description 1
- 238000005187 foaming Methods 0.000 description 1
- 239000000295 fuel oil Substances 0.000 description 1
- 150000004676 glycans Chemical class 0.000 description 1
- 231100001261 hazardous Toxicity 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 230000002209 hydrophobic effect Effects 0.000 description 1
- NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical compound O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 description 1
- 229910052749 magnesium Inorganic materials 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 239000003921 oil Substances 0.000 description 1
- 239000005416 organic matter Substances 0.000 description 1
- 238000013021 overheating Methods 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 229920000058 polyacrylate Polymers 0.000 description 1
- 229920001282 polysaccharide Polymers 0.000 description 1
- 239000005017 polysaccharide Substances 0.000 description 1
- 229920002451 polyvinyl alcohol Polymers 0.000 description 1
- 235000015497 potassium bicarbonate Nutrition 0.000 description 1
- 229910000028 potassium bicarbonate Inorganic materials 0.000 description 1
- 239000011736 potassium bicarbonate Substances 0.000 description 1
- TYJJADVDDVDEDZ-UHFFFAOYSA-M potassium hydrogencarbonate Chemical compound [K+].OC([O-])=O TYJJADVDDVDEDZ-UHFFFAOYSA-M 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 230000002265 prevention Effects 0.000 description 1
- 238000005086 pumping Methods 0.000 description 1
- 238000001223 reverse osmosis Methods 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 239000010959 steel Substances 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 229910052717 sulfur Inorganic materials 0.000 description 1
- 239000011593 sulfur Substances 0.000 description 1
- 238000012360 testing method Methods 0.000 description 1
- 239000002341 toxic gas Substances 0.000 description 1
- 210000002700 urine Anatomy 0.000 description 1
- 125000002348 vinylic group Chemical group 0.000 description 1
- 239000003643 water by type Substances 0.000 description 1
- 229920003169 water-soluble polymer Polymers 0.000 description 1
- 238000003466 welding Methods 0.000 description 1
Classifications
-
- A—HUMAN NECESSITIES
- A62—LIFE-SAVING; FIRE-FIGHTING
- A62D—CHEMICAL MEANS FOR EXTINGUISHING FIRES OR FOR COMBATING OR PROTECTING AGAINST HARMFUL CHEMICAL AGENTS; CHEMICAL MATERIALS FOR USE IN BREATHING APPARATUS
- A62D1/00—Fire-extinguishing compositions; Use of chemical substances in extinguishing fires
-
- A—HUMAN NECESSITIES
- A62—LIFE-SAVING; FIRE-FIGHTING
- A62C—FIRE-FIGHTING
- A62C3/00—Fire prevention, containment or extinguishing specially adapted for particular objects or places
-
- A—HUMAN NECESSITIES
- A62—LIFE-SAVING; FIRE-FIGHTING
- A62D—CHEMICAL MEANS FOR EXTINGUISHING FIRES OR FOR COMBATING OR PROTECTING AGAINST HARMFUL CHEMICAL AGENTS; CHEMICAL MATERIALS FOR USE IN BREATHING APPARATUS
- A62D1/00—Fire-extinguishing compositions; Use of chemical substances in extinguishing fires
- A62D1/0028—Liquid extinguishing substances
- A62D1/005—Dispersions; Emulsions
-
- E—FIXED CONSTRUCTIONS
- E21—EARTH OR ROCK DRILLING; MINING
- E21F—SAFETY DEVICES, TRANSPORT, FILLING-UP, RESCUE, VENTILATION, OR DRAINING IN OR OF MINES OR TUNNELS
- E21F15/00—Methods or devices for placing filling-up materials in underground workings
- E21F15/005—Methods or devices for placing filling-up materials in underground workings characterised by the kind or composition of the backfilling material
Landscapes
- Emergency Management (AREA)
- Business, Economics & Management (AREA)
- Chemical & Material Sciences (AREA)
- Mining & Mineral Resources (AREA)
- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Geochemistry & Mineralogy (AREA)
- Dispersion Chemistry (AREA)
- Geology (AREA)
- General Life Sciences & Earth Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Health & Medical Sciences (AREA)
- Public Health (AREA)
- Fire-Extinguishing Compositions (AREA)
- Processes Of Treating Macromolecular Substances (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Fireproofing Substances (AREA)
- Solid-Sorbent Or Filter-Aiding Compositions (AREA)
Abstract
The invention relates to a method for extinguishing coal mine shaft fires, consisting in: fully or partially swelling at least one superabsorbent (co)polymer in the presence of water, and subsequently injecting the resulting fully or partially swollen superabsorbent (co)polymer(s) directly into the shaft. The invention also relates to the unit used to perform said method.
Description
1 METHOD OF EXTINGUISHING COAL MINE FIRES AND INSTALLATION FOR IMPLEMENTING THE METHOD Coal mines have always constituted a safety problem. Some unexploited mines have 5 been burning for centuries. However, the number of fires increased considerably starting with the exploitation of coal for the production of steel or energy. These fires are often started by accidents or overheating of equipment (tractors, conveyor belts, welding, etc.), and once started, the fire can be spread by the gases 10 present in the galleries, especially methane and hydrogen. In other cases, fires on the surface spread underground, especially in mines that are not very deep (lightning, forest fires, incineration of refuse). 15 In certain cases, however, spontaneous combustion is observed, through gradual oxidation and build-up of heat, for example in the heaps at the pithead, in the case of coal contaminated with fuel oil, or in the presence of organic matter, for example in the form of wood-coal mixtures. This is in particular the case in the presence of pyrites which, on exposure to the atmosphere, tend to accelerate the phenomenon. 20 These coal fires are also frequent on the surface: heaps of fines or silos, especially in the presence of coal with a high sulfur content. China is a major home of such fires in the provinces of Xinjiang Uygur and Ningxia 25 Hui. These fires consume about 200 million tonnes of coal per year. For example, the Liu Huangou fire has been burning for 20 years and will burn for another 40 years with the extinguishing means currently employed, polluting the town of Urumqi with toxic gases (CO, H 2 S, C0 2 , etc.). 30 These fires cause caving-in and fissures which feed the pits with oxygen. Temperatures can exceed 800'C. The action taken consists in particular of injecting mud and earth for sealing these fissures. However, the latter are spread over wide areas and they are constantly changing, on ground that is often very hot and inaccessible. 35 The second country most affected is the United States of America and especially the large mines of Pennsylvania, where fires started around 1772. The largest fire began 2 in 1869 (Avondale, where the mine fire went out spontaneously after a year, after killing 110 people). There are currently 140 large coal mine fires in the USA. The conventional methods of fire extinguishing consist either of injecting mud for 5 blocking the air inlets and fissures, or of closing the galleries by means of walls of brick, cement or clay. However, the technique most used recently consists of injecting dense chemical foams with inert gas (N 2 - C0 2 ) or nitrogen directly. In certain regions, entire towns have been moved, and roads diverted, for example in Centralia. 10 The third country is India, where fires began in the 18th century. The Jharia mine is the world's largest mine fire, which started in 1916. Today, there are 70 fires in this very large coalfield, which is still in operation (coking coal). 15 The problem of fires in coal mine pits (and some surface mines) is far from being solved. In fact, injection of water is very ineffective as it trickles and infiltrates while evaporating to a slight extent. This does not provide sufficient cooling of the burning 20 coal. Water at the bottom of the mine can also evaporate and cause explosions due to the pressure. 25 The filling of fissures is random. In fact, over very large areas, there are numerous fissures, which are sometimes invisible. It is also dangerous to send trucks carrying earth and mechanical shovels above these combustion zones, which sometimes emit flames several meters high above the ground. 30 Dense foam laden with inert gas has a relatively high angle of repose and, on injection, can block the horizontal galleries, decreasing the horizontal transfers of oxygen. However, the foam does not have an extinguishing effect as it does not contain 35 sufficient water to cool the walls. The foam in fact disappears at relatively low temperatures (50 to 80'C).
3 In the case of injection of mud, for example bentonite mud, the mud has a tendency to flow like water and to separate at the bottom of the pits. Moreover, their very small angle of repose does not permit the sealing of horizontal galleries. 5 Tests were carried out in Australia (Controlling underground heating using Innovative Fire suppressant Injection - Proof of concept study - Shenggen Hu, Sheng Xue - SCIRO project (14021, Feb 2009) using a solution of polymer (polyacrylamide, carboxymethyl cellulose, acrylamide-xanthan acrylate copolymer) mixed with an aluminum complex (citrate in particular). The mixture is injected in 10 liquid form in the presence of a crosslinking agent. In other words, the mixture crosslinks after injection leading to the formation of a gel after a certain time. This liquid does not initially have an angle of repose and only coats the bottom of the galleries unless it is stored between two walls, which is difficult to achieve. Moreover, chemical manipulations consisting of extemporaneous mixing of 15 crosslinking agent and polymer near fires at high temperature are always hazardous. Particularly in China, polymers have been used as binders and water retainers for the production of gels or mineral pastes containing silica, kaolin, bentonite, fly ash, various muds, etc., which serve to seal the air inlets in coal mines that are on fire. 20 We may mention: 1 - Gel retarder for fire prevention and extinguishing - its application for spontaneous combustion of coal seams Wen, Hu; Xu, Jingcai; Dai, Aiping 25 Proceedings - Annual International Pittsburgh Coal Conference (1998), 15th, 593 597 CODEN PICNE4; ISSN. 1075-7961 2 - Thickening colloid for treating coal seam fire Zhu, Hongqing, Suo, Hongli; Zhang, Teng; Liu, Min; Ma, Lin; Wang, Yi; Yuan, 30 Huiping; Guo, Aidong; Zhao, Feng; Liu, Defeng; Zhang, Xinya Faming Zhuanli Shenqing, 6pp. CODEN CNXXEV 4 3 - Extinguishing spontaneous combustion in coal seam with heat-resistant, rich water gel Xu, Jingcai; Deng, Jun; Wen, Hu; Guo, Xingming; Zhang, Xinghai Mining Science and Technology '99, Proceedings of the International Symposium on 5 Mining Science and Technology, Beijing, China, Aug. 29-31, 1999 (1999), 137-140. Editor(s): Xie, Heping; Golosinki, Tad S. Publisher: A. A. Balkema, Rotterdam, Neth. CODEN: 69BDV4 4 - An inorganic foaming gel for preventing spontaneous combustion in a top-coal 10 falling region Yu, Shui-jun; Yu, Ming-gao; Feng-cheng; Pan, Rong-kun; Lu, Lai-xiang; Chang, Xu hua Zhongguo Kuangye Daxue Xuebao (2010), 39(2), 173-177 COden: ZKDXER 15 5 - Production of a composite gel material for the fireproofing and fire-extinguishing of coal seams Suo, Hongli; Zhu, Hongqing; Guo Aidong; Zhang, Teng; Yuan, Huiping; Wu, Ziping; Yan, Binjie Faming Zhuanli Shenqing, 5pp. CODEN: CNXXEV 20 6 - Acrylamide-type copolymer as blocking agent for fire control in coal seams Cao, Dacheng; Wen, Hu; Zhang, Xinhai; Li, Bo; Wang, Jingang; Liu, Qingning; Liu, Guicheng Faming Zhuanli Shenqing Gongkai Shuomingshu, 5pp. CODEN: CNXTEV 25 7 - The technique of fire extinguishing with gel for coal spontaneous combustion in fully mechanized caving face Wen, Hu; Xu, Jingcai; Deng, Jun; Zhang, Xinhai Proceedings in Mining Science and Safety Technology, [International Symposium], 30 Jiaozuo, China, 2002 (2002), 448-452. Editor(s): Zhang, Chuanxiang; Jing, Guoxun; Zhou, Ying. Publisher: Science Press, Beijing, Peop. Rep. China. CODEN: 69DDL4; ISBN: 7-03-010255-X In all these cases, it is the mineral portion, more or less dehydrated by the heat, 35 which serves to seal the oxygen passages to extinguish the fire. However, these methods are effective for small fires but are ineffective for large fires with ground subsidence.
5 There has been very limited success in extinguishing coal mine fires and it is often decided to abandon the regions and leave the fire to spread for decades in view of the costs and the slight chance of success. 5 The objective of the invention is therefore to develop a method of extinguishing coal mine fires combining the following characteristics: - Limited cost, - Application of a large amount of water, - Angle of repose of the injection fluid making it possible to obstruct 10 horizontal galleries, - Storage of injection fluids in intermediate horizontal zones for cooling the walls, - Filling of cavities even of large size, - Mobility of the injection fluids as changes of shape occur within the 15 mine or on the surface. The applicant has developed a method for solving all of these problems by using superabsorbent (co)polymers or SAPs with a high degree of swelling in water. By definition, these polymers are crosslinked. The polymers according to the invention 20 are injected in the form of partially or completely swollen superabsorbents, in contrast to the prior art. There are numerous types of natural or synthetic water soluble polymers that are crosslinked, or that can be crosslinked: polyvinyl alcohol, guar, alginates, carboxymethyl cellulose, dextran, xanthan, poly(ethylene oxide), etc. 25 The superabsorbents are polymers that are well known in specialty chemistry. They are generally in the form of powder. Their structure, based on a three-dimensional network that can be likened to a multitude of small cavities, each of them having the capacity to deform and to absorb water, confers on them the ability to absorb very large amounts of water and therefore to swell. Such polymers are described for 30 example in patent FR 2 559 158, which describes crosslinked polymers of acrylic or methacrylic acid, crosslinked graft copolymers of the polysaccharide / acrylic or methacrylic acid type, crosslinked terpolymers of the acrylic or methacrylic acid / acrylamide / sulfonated acrylamide type and their salts of alkaline-earth metals or alkali metals. 35 6 As already mentioned, the main characteristic of these polymers is a strong capacity to swell in aqueous medium. They can absorb and store large amounts of water up to 100 times their mass or more. They are used notably in agriculture for water retention in soils, in hygiene products for babies intended to contain urine and similar 5 applications. The invention therefore relates to a method of extinguishing fires in coal mine pits consisting of: - partially or completely swelling at least one superabsorbent (co)polymer in the 10 presence of water, - then injecting at least the swollen superabsorbent (co)polymer(s) obtained directly into the mine. Advantageously, the polymers are selected from the group comprising: 15 - crosslinked copolymers obtained by polymerization of acrylamide and of partially or completely salified acrylic acid, preferably in the form of a sodium salt, - crosslinked polyacrylic acids, partially or completely salified, preferably in the form of a sodium salt, which is more sensitive to 20 the salinity of the water and in particular to Ca and Mg 2 +. In a preferred embodiment, the polymers are crosslinked copolymers of acrylamide and of partially or completely salified acrylic acid and contain between 40 and 90 mol% of acrylamide and between 10 and 60 mol% of partially or completely salified 25 acrylic acid. In a particular embodiment, the SAP is a crosslinked terpolymer obtained by polymerization of acrylamide and/or of partially or completely salified acrylic acid and/or of partially or completely salified ATBS (acrylamido tert-butylsulfonate) 30 and/or of NVP (N vinylpyrrolidone). Other hydrophilic monomers, but also monomers of hydrophobic character, can be used for producing the polymers. 35 7 The SAP is partially or completely swollen. A completely swollen SAP is characterized in that all the small cavities of the three-dimensional network are filled with water to saturation, i.e. at a level such that on adding more water, the SAP does not absorb any additional water. 5 The polymers are crosslinked with 100 to 6000 ppm of at least one crosslinking agent selected from the group comprising acrylic compounds for example methylene bis-acrylamide, allylic compounds for example tetra-allylammonium chloride, vinylic compounds for example divinyl benzene, diepoxy, metal salts etc. 10 These polymers have a stability of several years in the ground. It can be improved by carrying out a double crosslinking with an acrylic crosslinking agent, preferably at a rate of 100 to 1000 ppm and an allylic crosslinking agent, 15 preferably at a rate of 1000 to 5000 ppm, for example MBA (methylene bis acrylamide) and tetraallylammonium chloride, which extends the stability of the SAP to more than 5 years. The swelling of these SAPs in distilled water generally reaches 150 to 200 times, but in a standard drinking water, about 100 times and less for very saline waters. 20 Therefore 10 kg of polymer and 990 kg of water are required to make a tonne of "solid water" for swelling of 100 times. The polyacrylamides have the capacity to produce swollen SAPs that are more rigid 25 and less sensitive to divalent metals than the polyacrylates. Advantageously, the water used for swelling the polymer has the lowest possible salinity, so as to obtain the maximum swelling of the SAP for a given amount. The water preferably contains less than 200 g/l, very preferably less than 100 g/l of salts, 30 for example NaCl, CaCl 2 , MgCl 2 . For this purpose, it can be treated by reverse osmosis. When the SAPs are swollen, the angle of repose of the SAPs varies as a function of the initial granulometry of the SAP. With a granulometry of less than 1 mm (less 35 than about 5 mm swollen), the angle of repose is of the order of 10'. With a granulometry of less than 4 mm (less than about 1.5 cm swollen), the angle can reach 15-20'. It is therefore possible to block galleries simply by injection.
8 In contact with a wall that is on fire, the stored water evaporates and the polymer is burnt. However, for 1 g of polymer, 100 g of water has evaporated, or an energy absorption of 226 kJ, to which must be added the heat for temperature rise of the steam generated to 400-600'C. For example, with a flow rate of 1000 1/minute, it is 5 possible to remove 4000 MJ/min, to be compared with the heat of combustion of 1 liter of gas oil of 36 MJ. The swollen superabsorbent therefore has both a mechanical effect like a rigid foam, and a thermal effect like water which has a formation of steam of 1.7 m 3 per liter of 10 water evaporated, and the vapor of which does not dissociate into dioxygen and dihydrogen, explosively, not before 1600'C. Moreover, it can deform as a function of the movements of the ground, maintaining their sealing function. It is also possible to add to the water and/or with the swollen SAP, compounds 15 improving the extinguishing power of this water with additive. It can be ammonium phosphates, potassium bicarbonate, urea etc. However, salts dissolved in the water reduce the swelling. Thus, urea is preferred. Still according to the invention, the swollen SAP is prepared in a zone away from the 20 fire, thus avoiding any dangerous manipulation near flames. The swollen SAP is then transported and then injected by tanker truck under pressure or by pipeline. The partially or completely swollen SAP can be formed continuously or discontinuously. 25 In practice, the partially or completely swollen SAP is injected at the pithead, in vertical or vertical horizontal boreholes or in surface fissures. The invention also relates to an installation employing the method described above 30 and comprising: - a means of storing the superabsorbent (co)polymer, - a means of dosing the superabsorbent (co)polymer, - a means of dosing water, - a means of mixing the water and the superabsorbent (co)polymer, 35 - a means of pumping the partially or completely swollen superabsorbent (co)polymer obtained, 9 - a means of injecting the partially or completely swollen superabsorbent (co)polymer into the mine. Advantageously, the means of mixing the water and the superabsorbent (co)polymer 5 is in the form of two successive tanks, permitting continuous and uniform swelling of the superabsorbent. The invention and the advantages resulting therefrom will be clearer from the following example, together with the appended drawings. 10 Fig. 1 is a representation of an installation employing the method of the invention according to a first embodiment. Fig. 2 is a representation of an installation employing the method of the invention according to a second embodiment. 15 The superabsorbent is supplied in big bags of 750 to 1000 kg, in containers of 2 to 5 tonnes (1) (see Fig. 1) or in a tanker truck (1) (see Fig. 2), then stored in a hopper or a silo (2). It is dosed by a dosing screw (3) in a continuous system with 2 tanks (4, 5) equipped with a powerful propeller or spiral stirrer (6, 7). The superabsorbent (1) and 20 water (8) are metered into the first swelling chamber (4), the water being in excess relative to the swelling of the (co)polymer (e.g. 1200 liters per hour for 10 kg swelling 100 times), which permits more efficient stirring. The residence time required depends on the granulometry and is between 1 hour (less than 1 mm) and 3 hours (less than 4 mm). The second tank (5) operates with a high level-low level 25 stopping the metering screw (3) and water inlet (8) at the top. The swollen SAP is pumped either by means of a pump of the Moineau type (9) up to pressures of about 10 bar or by means of a piston pump up to 200 bar. 30 The swollen SAP is then injected by means of a injection tube (10) at the pithead or in vertical or vertical horizontal boreholes or in surface fissures. The amount of water required for extinguishing is difficult to calculate as a proportion of the volume will be vaporized. But it is hundreds or thousands of tonnes 35 of water, bearing in mind that a tonne of water requires about 10 kg of superabsorbent.
10 A person skilled in the art can adapt these basic conditions to the local characteristics of the fires. In particular, it will be possible to supply the fissures by tanker truck with swollen SAP remaining at a distance from the fire zone. The product can be conveyed from the truck by a pump or by pressurization. The method is much easier 5 to apply than trucks bringing soil, which have to move over ground that is both hot and unstable.
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PCT/FR2012/050050 WO2012063009A2 (en) | 2012-01-09 | 2012-01-09 | Method for extinguishing coal mine fires and unit for performing said method |
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EP (1) | EP2802385A2 (en) |
CN (1) | CN104428038A (en) |
AU (1) | AU2012202891A1 (en) |
CA (1) | CA2858655A1 (en) |
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CN104989444A (en) * | 2015-06-05 | 2015-10-21 | 安徽理工大学 | Colloid foam material for preventing and controlling coal spontaneous combustion and preparing method of colloid foam material |
CN106237563B (en) * | 2016-08-16 | 2021-08-31 | 华电电力科学研究院有限公司 | Intelligent flame retardant spraying system and method based on coal quality |
CN108498998B (en) * | 2018-03-30 | 2021-07-20 | 中煤科工集团重庆研究院有限公司 | Composite fire extinguishing material for coal mine and preparation method thereof |
CN110496343B (en) * | 2018-05-18 | 2021-02-23 | 山东昊月新材料股份有限公司 | Multipurpose fire extinguisher |
RU2763214C1 (en) * | 2021-01-11 | 2021-12-28 | Федеральное государственное автономное образовательное учреждение высшего образования "Сибирский федеральный университет" | Method for extinguishing borehole fires with a powder extinguishing agent |
CN114200043B (en) * | 2021-12-01 | 2023-09-05 | 中煤科工集团沈阳研究院有限公司 | System and method for detecting coal natural ignition sign gas and gas storage device thereof |
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US8096622B2 (en) * | 2007-09-25 | 2012-01-17 | Micon | Method of controlling mine fires with polymeric gel |
CN101392657A (en) * | 2008-10-22 | 2009-03-25 | 河北金牛能源股份有限公司葛泉矿 | Pulping system for preventing coal spontaneous combustion |
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- 2012-01-09 AU AU2012202891A patent/AU2012202891A1/en not_active Abandoned
- 2012-01-09 WO PCT/FR2012/050050 patent/WO2012063009A2/en active Application Filing
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EP2802385A2 (en) | 2014-11-19 |
CN104428038A (en) | 2015-03-18 |
CA2858655A1 (en) | 2012-05-18 |
RU2014125244A (en) | 2016-01-20 |
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