前苏联专利SU1190995A3 Method of tightening and sealing geological rock and soil formations and coal deposits

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专利摘要:
Waterglass solutions are mixed with polyisocyanates and these emulsions are then left to harden in the formations. Introduction of the mixture into the formations which are required to be consolidated, e.g. deposits of coal, is mainly carried out by forcing the mixture under pressure into bore-holes in the formations. According to one variation of the process, the components of the mixture are introduced into the multi-chamber cartridges which are introduced into the bore-holes and then destroyed as the components are mixed. Certain additives such as accelerators, blowing agents, polyols, stabilizers and/or thixotropic agents are advantageous for the quality of the composite masses formed by hardening of the mixture.
公开号:SU1190995A3
申请号:SU802890299
申请日:1980-03-05
公开日:1985-11-07
发明作者:МЕЙЕР Франк；Мехеш Ханс；Кубенс Рольф；Винкельманн Мартин
申请人:Бергверксфербанд Гмбх (Фирма)；Байер Аг (Фирма)；
IPC主号:

专利说明:

1 The invention relates to the development of coal deposits and can be used to strengthen various stone and earth formations and coal deposits. The aim of the invention is to increase the strength of the seal. The polyisocyanates used in this process as a curing agent can, in principle, be any organic polyisocyanates having aliphatic, cycloaliphatic, araliphatic, aromatic or heterocyclic related poly isocyanate groups, but it is preferable to use polysocyanates. aromatic bound polyisocyanate groups are commonly used in polyurethane chemistry that are liquid at room temperature, for example 2,4-diisocyanatotoluene 2 b-diisocyanatotoluene and any mixtures of these isomers (TDI), polyphenyl polymethylene polyisocyanates which can be prepared by the condensation of aniline / formaldehyde followed by phosgeneration (MDI), and derivatives of these polyisocyanates which contain carbodium, biuret, urethane, or allophanate groups and are liquid at room temperature. emperatzfe .. Preferred for use herein are CDI poliizotsiaiatna mixture obtained fosgenatsiey comrade condensation of aniline and formaldehyde, and isocyanate-containing; Products of interaction with polyhydric alcohols (polyols). Solutions of liquid glass are understood to be solutions of sodium silicate and / or potassium hydroxide in water. Commercial raw materials may also be used, possibly containing, for example, calcium silicate, magnesium silicate, borates and aluminates. The molar ratio of SiO: N20 (M -) can vary from 0.5: 1-4: 1, 1: 1-2.5: 1. The concentration of the liquid glass solution can be selected in a diagonal range of 25–55 wt.% 5, preferably 40–50 wt.%. . The preparation of mixtures of polyisocyanates and liquid glass solutions is a simple procedure5 it is only necessary to mix the two liquids uniformly, i.e. manual method. using blades for mixing or conventional 952 stirrs with an ohm drive. Emulsions can also be prepared in mixing or metering devices, in this case, two liquids are fed to the mixer with a through flow from the metering pump. Dosing pumps can be, for example, gear, piston or diaphragm. The through-flow mixers are, for example, mixing chambers with driven agitators or static mixers, for example tubes with differently mounted partitions. The mixture is mainly pumped into the deposit or holes in the deposit through a lance or pipe. The holes should be closed immediately after the mixture is injected, since gelatination and the subsequent solidification of the mixture occurs only after 30-60 seconds. If the mixture is to be introduced into the holes, it is recommended to insert through the holes holes that act as valves. Depending on the nature of the polyisocyanate, the blending method chosen, the desired degree of foaming of the sealing agent and its consistency, you can add a trace of the polyisocyanate or to the liquid glass diluent or to the mixture of half a half of the cyanate and liquid glass solution, 1, catalysts commonly used in polyurethane chemistry, for example, organo-metagenic compounds — dcbutyldylate tin and tertiary amines (triethylamine) in the amount of di% by weight, based on SMYA.Yuy: shelves of a cyanate and a solution of liquid glass, .2, Gas section disintegrating agents, for example acetone, methylene chloride, monofluorochloromethane, dichlorodifluoromethane and butane,: in amounts up to 30%. by weight, based on a mixture of polyisocyanate and liquid glass solution, 3, Compounds having at least one group reactive with respect to polyisocyanate, to the reaction mixture in amounts up to 30% by weight, based on a liquid glass solution. Organic polyamines, such as ethylene diamine, dystilenetriamine 5, triethylentetramine, 4,4-diaminodiphenylmethane, or 2,4-diaminotoluene, can be used, but organic compounds having alcoholic and hydroxyl groups are preventative. They include simple
monohydric or polyhydric, preferably polyhydric, alcohols (mol. wt. 32-200, preferably 62-200) or common polyhydroxyl compounds with a relatively high molecular weight (mol. wt. 200-500, preferably 200 1000), commonly used polyesters or polyhydroxy polymers of ethers. Among low molecular weight alcohols, methanol, ethanol, propanol, ethylene glycol, diethylene glycol, triethylene glycol, glycerin, and trimethylolpropane can be used, and alcohols of relatively high molecular weight — polyethers of dicarboxylic acids, such as phthalic, adipic acid, such as phthalic, adipic acid, such as phthalate, adipine, hexadequate, adipine, hexane, adipine, adipine, polyester, such as phthalate, adipic acid, glycol, and trimethylol propane. acids and / or maleic acid and said simple alcohols or polyethers of polyhydric alcohols, such as can be obtained by the introduction of the alkoxy group, t. that is, in particular by chemically adding propylene oxide and / or ethylene oxide to the starting molecules with low molecular weight. Water and, for example, said low molecular weight amines or alcohols, which have at least 2 active hydrogen atoms, are suitable as starting molecules. I
Preferably the use of these polyesters of polyhydric alcohols with the number of hydroxyl groups 50600. Alcohols can be added to a liquid glass solution or to a polyisocyanate or as a third component to the mixture of polyisocyanate and liquid glass.
4. Emulsifiers, for example, the reaction products of stearylamine and ethylene oxide, polyether esters of abietic acid or oleic acid and ethylene oxide, polyglycol ethers fatty alcohols, alkylphenol polyglycol ethers, emulsifiers, based on liquid glass, for example Tegosivin, made by the company’s amphogenic seeds, for example, Tego - Retain 27 from Goldschmit AG, and fatty acid amidoalkyldimethylamine oxides, for example amino acid WS 25 from Goldschmit AG. These emulsifiers in particular contribute to the emulsification of the compound according to item 3 in the liquid glass component and, therefore, contribute to the complete mixing of all the components.
Emulsifiers are generally added in amounts of up to 15% by weight, based on a mixture of MDI and a solution of water glass.
5.Tixotropic agents, such as powdered asbestos or other surfactants alone or mixed with emulsifiers as specified in paragraph A. These thixotropic agents are preferred when using mixtures of liquid glass solution and the compounds mentioned in paragraph 3. They also make it possible for emulsions remain stable for a significant period so that two-component systems containing the packaging of a solution of liquid glass and additives in paragraphs 1-4 and the packaging of the polyisocyanate can be discharged from Stach sealing. Thixotropic agents generally add
in amounts up to 5% by weight, based on a mixture of polyisocyanate and a solution of liquid glass.
6. Foam stabilizers, for example organo-polysiloxanes, known from the chemistry of polyurethanes.
Any of these additives can be added alone or in combination with the other, both to the mixture and to the components, before they are mixed.
Multi-chamber capsules containing polyisocyanate, a solution of liquid glass and, if necessary, additives in separate containers can also be introduced into these holes. After the mechanical destruction of the capsules and the mixing of the liquid components, for example, by rotating a wooden or metal rod or anchor blade mixer, the hardening foam mixture enters under its own foam pressure into the formations intended for sealing and sealing, and at the same time also completely have a hole.
Used in examples 1-9 is a liquid glass 44% aqueous solution of sodium silicate
(Sic 2; Naj.0 2: 1);
MDI is a polyisocyanate obtained by phosgenation of formaldehydaniline condensate and containing more than 50% dinocyanatoiphenyl methane and 41% isocyanate, viscosity 95 mPa at 25 s.
Example 1. The edge of the used secondary wall passage should be strengthened during recessing, because, due to the strong loosening in the transition from the bottom to the driftway, mining can be prevented from causing the roof to collapse, which can lead to accidents when the coal falls.
At a distance of 3 m, a 2.5 m long well is drilled. These wells are injected with a mixture of liquid -glass and polyisocyanate, 300 kg each per well, both components of which the Ahydrous 44% component, the component Vopoliisocyanate MDI) are used in a ratio of Q: A 3: 1. After the resin has cured, the hardening of the roof is achieved. Roof collapse no longer occurs
PRI mme R 2. With the collapse of the reservoir & a parallel layer with a thickness of 20 cm begins to collapse. The layer of a layer 0.5 to 0.6 m thick collapses into large pieces, sometimes over a length of 15-2t) m. By injecting a mixture of liquid glass and polyistate () into the reinforced zone of the layer hardening of the entire parallel formation.
Example 3. In a layer of fat coal prone to spinning, at a distance of 4.5 m, a 4-meter-deep hole is drilled. To prevent slope formation in the coal face and roof collapse, a mixture of liquid glass and the product obtained by the exchange reaction of VDI with a polybasic alcohol (prepolymer, NCO - OH - molar ratio 1: 0.005; 180 kg of the mixture per well). Both components (liquid glass and prepolymer) are used in a 1: 1 ratio. After half an hour after the injection, coal can be dredged, without meeting the formation of slopes in the coal seam.
EXAMPLE 4 A similar coal face after the tests of Example 3 was strengthened with a mixture consisting of 44% liquid glass AND an exchange reaction product of MDI with a polybasic alcohol, the molar ratio
NCO: OH 1: 0.3
Both components are used in a 1: 1 ratio. Already 15 minutes after the end of the injection, you can start
Take a coal seizure without meeting the formation of slopes in the coal seam.
EXAMPLE 5 Hardening experiments were carried out on a coal-prone (gas-flame coal) 40 m long prone to creep. To this end, using a drilling machine, drill holes with a depth of 3.30-4.70 m per distance Q from SRI 4-4.5 m from each other at an angle of about 15 to the vertical and a mixture of 44% water glass and polyisocyanate solution is introduced through these wells, the mass ratio
5 components 1: 1. The mixture consumption per well is approximately 200 kg. After 2 hours after the mixture is introduced, coal mining can begin. Osypani ang. it is not observed.
0 Approx. The same coal seam after testing in Example 5 is reinforced with. using a mixture of 44% liquid glass and the product of the interaction of MDI with many
5 atomic alcohol (MDI-prepolymer), in an amount less equivalent. Molar ratio
NCO: OH G: 0.005. Both components are mass-based.
0 ratio of 1: 3. The mixture consumption per well is about 150 kg. Already after 20 minutes after the introduction of the mixture, it is necessary to start coal mining. No osteanide coal is observed. Same
a positive result is also achieved when using the product of the interaction of ALI with polyhydric alcohol, taken in an amount less than the equivalent, at a molar ratio
NCO: OH 1: 0.3.
The mass ratio of both components is 1: 3.
I. ,
Example 7. The hardening tests were carried out in the same coal seam as in examples 5 and 6. For hardening, a mixture consisting of 44% of liquid glass and the product of the reaction of MDI with hnogoatom alcohol was used in an amount less equivalent. Molar ratio;
NCO: OH 1: 0.3.
The mass ratio of both components is 5 17: 3. Mixture consumption per well is about 130 kg. 30 minutes after the completion of the hardening process, i.e. the introduction of the mixture into the wells, coal mining can begin. The grazing coal is not observed. The same positive result on the strengthening of the formation was obtained when using a mixture consisting of liquid glass and the product of the interaction of MDI with a polyhydric alcohol, in an amount less than the equivalent, at a molar ratio of NCO: OH 1: 0.005. The mass ratio of both components is 17: 3. After conducting the hardening experiments described in Examples 5-7, comparative tests were carried out in the same bottomhole using 44% water glass and known hardeners, namely a 33% calcium chloride solution and ethyl acetate. Example In the coal bed, which is prone to crawling, a hole is drilled 4.5 m deep at a distance of 3 m from one another. A mixture consisting of 44% water glass and a 33% calcium chloride solution is introduced into the drilled wells at a mass ratio of 1: 3. Extraction of coal begins 4 hours after the end of the introduction of the mixture. At the same time, it has been established that hardening of the formation does not occur; coal cannot be prevented from falling off. And with a different weight ratio of both components, the desired result is not achieved. Example 9. Three tests were carried out in which ethyl acetate was used as an opening for curing 44% water glass. In the first experiment, a mixture consisting of liquid glass and ethyl acetate, taken in a weight ratio of 1: 3, was used for strengthening. In the second experiment, the mass ratio of liquid glass and ethyl acetate is 17: 3, in the third - 1: 1. The development of coal begins 5 hours after the start of the introduction of the mixture. There is no formation hardening. Thus, precipitation of the coal cannot be prevented. The table gives the results of the seal strength test. As can be seen from the table, prepared from liquid glass and calcium chloride, respectively, liquid. glass and ethyl acetate, the samples do not have the strength (expressed in terms of compressive strength) -. These mixtures do not provide a setting (expressed through the strength of setting) with a rock and a charcoal. This explains the negative results obtained in practice. To determine the compressive strength of the proposed and known mixtures, samples were prepared for tests measuring 4x4x4 cm, which were subjected to a compression test. To determine the strength of the setting, pieces of natural stone or coal, size 4x4x4, are broken, the fragments of the broken piece are fixed in shape at a distance of 5 mm: between fracture surfaces and poured with the proposed or known mixtures. After 24 hours, the strength of the glued prisms for bending is determined, which is taken as a measure of the gluing capacity. The adhesiveness of these mixtures is judged by the strength of the setting with stone and coal.
eleven
Sun + MDI 1: 3
17: 3 1: 1
Sun + MDI for.1
0.15
0.2 0.2 0.3 0.15 0.15 3.9
4.2
1: 3
17: 3
Sun + VDI-form.2
1: 1
1: 3
Sun-MDI-form.2
17: 3
1: 3 BC + H1
17: 3
1: 1
Sun + H2
1: 3
17: 3
1: 1 P
2 0.2
2.2
0.3
4.1
4.9 6
2.5
1.9
0.7
0.3
ABOUT
ABOUT
ABOUT
ABOUT
ABOUT
ABOUT
ABOUT
Ltd
ABOUT
A: BC-liquid glass 44% solution, MDI-For. 1 The product of the interaction of MDI with a polyhydric alcohol, which is taken in an amount less than the equivalent, MSO: OH - molar ratio equal to 1: 0.005, MDI-forma.2 - the product of the interaction of MDI with a polyhydric alcohol, which is taken in a quantity less than the equivalent, HCO: OH is the molar ratio equal to G: 0.3, HI is the hardener: 33% calcium chloride solution, H2 is the hardener: ethyl acetate.

权利要求:
Claims (1)
[1]
. METHOD OF SEALING AND HERMIZATION OF GEOLOGICAL STONE ROCK AND EARTH FORMATIONS AND COAL DEPOSITS by treating them with a mixture of liquid glass and hardener, characterized in that, in order to increase the strength of the seal, a mixture of polyisocyanates obtained by condensation is used as a hardener aniline and formaldehyde, or containing isocyanate groups or the product of the interaction of this mixture with polyols at a _β weight ratio of hardener and S of water glass of 3: 1-17.
56606 N ^{, D} Ti ^

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同族专利:

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公开号 | 申请日 | 公开日 | 申请人 | 专利标题

BE556490A|1956-04-16|

DE1784458U|1957-10-02|1959-03-05|Ind Companie Kleinewefers Kons|TEMPERATURE SENSORS, IN PARTICULAR FOR HEAT EXCHANGERS.|

DE1758185U|1957-10-18|1957-12-19|Schanzenbach & Co Gmbh|DEVICE FOR FIXING THE ENDS OF ELECTRICAL CABLES, COMBINED IN HOLE, SLOTTED OR BLOCK TERMINALS.|

US3181611A|1961-06-29|1965-05-04|Dow Chemical Co|Selective prevention of water and brine intrusion into mineral producing strata|

GB1186771A|1967-05-12|1970-04-02|Conteki Dev Ltd|Silicious Products|

DE1914554C3|1968-03-21|1978-10-12|Kabushiki Kaisha Takenaka Komuten, Osaka |Method for sealing ground formations and civil engineering structures|

US3637019A|1970-03-16|1972-01-25|Dalton E Bloom|Method for plugging a porous stratum penetrated by a wellbore|

US3719050A|1970-06-01|1973-03-06|Toho Chem Ind Co Ltd|Soil stabilization method|

US3805531A|1970-12-21|1974-04-23|Minnesota Mining & Mfg|Consolidation of mineral aggregate|

DE2310559C3|1973-03-02|1975-09-11|Bayer Ag, 5090 Leverkusen|Foam concrete, a process for its manufacture and its use for the manufacture of building elements|

DE2325090C3|1973-05-17|1980-11-06|Bayer Ag, 5090 Leverkusen|Process for the production of an inorganic-organic polymer-polysilicic acid composite material in the form of a colloidal xerosol|

US3882684A|1973-09-12|1975-05-13|Bergwerksverband Gmbh|Two-compartment cartridge adapted for use in strengthening coal or stone walls|

DE2346740B2|1973-09-17|1978-11-30|Bergwerksverband Gmbh, 4300 Essen|Process for sealing the gas space of salt caverns against soil salt solutions|

US4139676A|1974-02-12|1979-02-13|Minnesota Mining And Manufacturing Company|Consolidation of aggregate material|

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US4056937A|1976-01-08|1977-11-08|Kyokado Engineering Co. Ltd.|Method of consolidating soils|

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法律状态:

优先权:

申请号 | 申请日 | 专利标题

DE2908746A|DE2908746C2|1979-03-06|1979-03-06|Process for consolidating and sealing geological and poured rock and earth formations|

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