GB1576943A - Filling cavities underground - Google Patents
Filling cavities underground Download PDFInfo
- Publication number
- GB1576943A GB1576943A GB26327/79A GB2632779A GB1576943A GB 1576943 A GB1576943 A GB 1576943A GB 26327/79 A GB26327/79 A GB 26327/79A GB 2632779 A GB2632779 A GB 2632779A GB 1576943 A GB1576943 A GB 1576943A
- Authority
- GB
- United Kingdom
- Prior art keywords
- cement
- agent
- concrete
- slurry
- cavity
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired
Links
- 239000002002 slurry Substances 0.000 claims description 52
- 239000003795 chemical substances by application Substances 0.000 claims description 46
- 239000000463 material Substances 0.000 claims description 44
- 239000004568 cement Substances 0.000 claims description 42
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 claims description 29
- BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 claims description 25
- 230000003319 supportive effect Effects 0.000 claims description 21
- GSEJCLTVZPLZKY-UHFFFAOYSA-N Triethanolamine Chemical compound OCCN(CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-N 0.000 claims description 18
- 239000000203 mixture Substances 0.000 claims description 16
- 229910000029 sodium carbonate Inorganic materials 0.000 claims description 15
- 238000000034 method Methods 0.000 claims description 14
- 239000003245 coal Substances 0.000 claims description 13
- 229910000027 potassium carbonate Inorganic materials 0.000 claims description 12
- 239000011396 hydraulic cement Substances 0.000 claims description 6
- 239000002699 waste material Substances 0.000 claims description 4
- 238000007789 sealing Methods 0.000 claims description 2
- 229960004418 trolamine Drugs 0.000 description 16
- ONCZQWJXONKSMM-UHFFFAOYSA-N dialuminum;disodium;oxygen(2-);silicon(4+);hydrate Chemical compound O.[O-2].[O-2].[O-2].[O-2].[O-2].[O-2].[O-2].[O-2].[O-2].[O-2].[O-2].[O-2].[Na+].[Na+].[Al+3].[Al+3].[Si+4].[Si+4].[Si+4].[Si+4] ONCZQWJXONKSMM-UHFFFAOYSA-N 0.000 description 10
- 229940080314 sodium bentonite Drugs 0.000 description 10
- 229910000280 sodium bentonite Inorganic materials 0.000 description 10
- 238000012360 testing method Methods 0.000 description 9
- 239000000126 substance Substances 0.000 description 8
- 239000011398 Portland cement Substances 0.000 description 7
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 5
- 229910000288 alkali metal carbonate Inorganic materials 0.000 description 4
- 150000008041 alkali metal carbonates Chemical class 0.000 description 4
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- 229940092782 bentonite Drugs 0.000 description 3
- 229910000278 bentonite Inorganic materials 0.000 description 3
- 239000000440 bentonite Substances 0.000 description 3
- SVPXDRXYRYOSEX-UHFFFAOYSA-N bentoquatam Chemical compound O.O=[Si]=O.O=[Al]O[Al]=O SVPXDRXYRYOSEX-UHFFFAOYSA-N 0.000 description 3
- 239000000470 constituent Substances 0.000 description 3
- 239000011440 grout Substances 0.000 description 3
- 230000003245 working effect Effects 0.000 description 3
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- VSCWAEJMTAWNJL-UHFFFAOYSA-K aluminium trichloride Chemical compound Cl[Al](Cl)Cl VSCWAEJMTAWNJL-UHFFFAOYSA-K 0.000 description 2
- 239000003518 caustics Substances 0.000 description 2
- VCJMYUPGQJHHFU-UHFFFAOYSA-N iron(3+);trinitrate Chemical compound [Fe+3].[O-][N+]([O-])=O.[O-][N+]([O-])=O.[O-][N+]([O-])=O VCJMYUPGQJHHFU-UHFFFAOYSA-N 0.000 description 2
- XGZVUEUWXADBQD-UHFFFAOYSA-L lithium carbonate Chemical compound [Li+].[Li+].[O-]C([O-])=O XGZVUEUWXADBQD-UHFFFAOYSA-L 0.000 description 2
- 231100000331 toxic Toxicity 0.000 description 2
- 230000002588 toxic effect Effects 0.000 description 2
- CWYNVVGOOAEACU-UHFFFAOYSA-N Fe2+ Chemical compound [Fe+2] CWYNVVGOOAEACU-UHFFFAOYSA-N 0.000 description 1
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
- 239000004115 Sodium Silicate Substances 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 238000002485 combustion reaction Methods 0.000 description 1
- 230000001419 dependent effect Effects 0.000 description 1
- 239000002360 explosive Substances 0.000 description 1
- 229940104869 fluorosilicate Drugs 0.000 description 1
- 230000003400 hallucinatory effect Effects 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 238000011065 in-situ storage Methods 0.000 description 1
- 229910052500 inorganic mineral Inorganic materials 0.000 description 1
- 238000009434 installation Methods 0.000 description 1
- 239000002085 irritant Substances 0.000 description 1
- 231100000021 irritant Toxicity 0.000 description 1
- 229910052808 lithium carbonate Inorganic materials 0.000 description 1
- 239000011707 mineral Substances 0.000 description 1
- 238000005065 mining Methods 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 231100000252 nontoxic Toxicity 0.000 description 1
- 230000003000 nontoxic effect Effects 0.000 description 1
- 239000011435 rock Substances 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 238000009416 shuttering Methods 0.000 description 1
- NTHWMYGWWRZVTN-UHFFFAOYSA-N sodium silicate Chemical compound [Na+].[Na+].[O-][Si]([O-])=O NTHWMYGWWRZVTN-UHFFFAOYSA-N 0.000 description 1
- 229910052911 sodium silicate Inorganic materials 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
- C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
- C04B18/00—Use of agglomerated or waste materials or refuse as fillers for mortars, concrete or artificial stone; Treatment of agglomerated or waste materials or refuse, specially adapted to enhance their filling properties in mortars, concrete or artificial stone
- C04B18/04—Waste materials; Refuse
- C04B18/12—Waste materials; Refuse from quarries, mining or the like
-
- C—CHEMISTRY; METALLURGY
- C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
- C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
- C04B40/00—Processes, in general, for influencing or modifying the properties of mortars, concrete or artificial stone compositions, e.g. their setting or hardening ability
- C04B40/06—Inhibiting the setting, e.g. mortars of the deferred action type containing water in breakable containers ; Inhibiting the action of active ingredients
- C04B40/0641—Mechanical separation of ingredients, e.g. accelerator in breakable microcapsules
- C04B40/065—Two or more component mortars
-
- 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
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02W—CLIMATE CHANGE MITIGATION TECHNOLOGIES RELATED TO WASTEWATER TREATMENT OR WASTE MANAGEMENT
- Y02W30/00—Technologies for solid waste management
- Y02W30/50—Reuse, recycling or recovery technologies
- Y02W30/91—Use of waste materials as fillers for mortars or concrete
Landscapes
- Engineering & Computer Science (AREA)
- Chemical & Material Sciences (AREA)
- Ceramic Engineering (AREA)
- Mining & Mineral Resources (AREA)
- Organic Chemistry (AREA)
- Materials Engineering (AREA)
- Structural Engineering (AREA)
- Civil Engineering (AREA)
- Environmental & Geological Engineering (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Life Sciences & Earth Sciences (AREA)
- Geochemistry & Mineralogy (AREA)
- Geology (AREA)
- Analytical Chemistry (AREA)
- Curing Cements, Concrete, And Artificial Stone (AREA)
- Lining And Supports For Tunnels (AREA)
Description
(54) FILLING CAVITIES UNDERGROUND
(71) We, COAL INDUSTRY (PATENTS)
LIMITED, a company organised in accordance with the laws of Great Britain of Hobart House,
Grosvenor Place, London, S.W.1X 7AE
England, do hereby declare the invention, for which we pray that a patent may be granted to us, and the method by which it is to be performed, to be particularly described in and by the following statement:
This invention concerns a method of preparing a supportive concrete-like material for at least partially filling a cavity in an underground mine.
In an underground mining installation, mine roadways are formed by tunnelling machines and subsequently supported by a series of roof supports arranged along their length. In order to further support the mine roadways, it is common practice to position a plurality of mine packs adjacent to the mine roadways. These packs conveniently comprise a concrete-like material and are positioned consecutively as the mine roadway advances. The concrete-like material has to set so that it can provide sufficient strength
to support the mine roadway within a pre
selected time, which is dependent upon the
rate of advance of mineral workings since
these workings are not permitted to progress
more than a prescribed distance beyond the
supported roadway.
Hitherto, quick setting cement has been
used as a constituent of a concrete-like
material so that the material sets or hardens
at a sufficiently rapid rate, ordinary Portland
cement not setting quickly enough to provide
sufficient strength sufficiently soon to support
the mine roadway.
Unfortunately, such quick setting cement is
expensive and moreover its operational setting
procedure may commence undesirably quickly
with respect to the supply of the remaining
constituents of the concrete-like material.
Furthermore, if operators using the quick
setting cement omit to wash pipes soon enough after passage of the quick setting cement therethrough, then the pipes will be blocked and unusable for subsequent operations owing to the presence of set cement therein.
One of the objects of the present invention is to mitigate the above mentioned problems.
According to the invention, the present invention provides a method of preparing a supportive concrete-like material for at least partially filling a cavity in an underground mine comprising adding a first aqueous slurry including hydraulic cement to the cavity and concurrently adding a second aqueous slurry including an agent for accelerating hardening of the cement and leaving the slurries to harden into a supportive concrete-like material in the cavity.
Preferably, the second slurry contains a dirt aggregate although the first slurry may
contain the dirt aggregate or it may be
apportioned between the first and second
slurries. The agent is preferably constituted
as defined above.
The dirt aggregate conveniently com
prises run-of-mine coal or it may contain
pit waste.
The accelerating agent for accelerating
hardening of cement preferably comprises
triethanolamine and at least one alkali metal
carbonate, and may be described and
claimed in our co-pending application Nos.
19554/77 and 33327/77 (Serial No.
1 576 942).
A preferred agent constitutes by weight
one and a half parts triethanolamine, five
parts sodium carbonate and one part
potassium carbonate.
In operation the agent preferably reacts
with cement in a ratio by weight of three
parts agent to forty parts weight of cement.
According to another aspect of the
invention, the present invention provides a
supportive concrete-like material for at least partially filling a cavity in an underground mine comprising a first aqueous slurry including hydraulic cement and a second aqueous slurry including an agent for accelerating hardening of the cement, the slurries after being combined together and hardening, forming the supportive concrete-like material within the cavity. The agent is preferably constituted as defined above.
The second slurry conveniently includes sodium bentonite.
The invention will now be described with reference to the accompanying drawings in which:
Figure 1 is a graph showing performance characteristics of cement including an accelerator, and
Figure 2 is a diagrammatic drawing of equipment installed in an underground mine.
In an underground coal mine, it is necessary to provide permanent support for roadways leading to and from workings in the mine. The permanent support conveniently comprises a concrete-like material including run-of-mine coal and a cementitious mixture.
The concrete-like material to support a particular roadway is required to harden or set sufficiently rapidly as to ensure that a coal face associated with the particular roadway does not advance further and a prescribed distance ahead of sufficiently hardened concrete-like material, since the concretelike material cannot support the roadway until it is sufficiently hardened. Operators in the roadway would be placed in jeopardy if the coal face were to advance further than the prescribed distance ahead of the support roadway without adequate supports.
The hardening rate of the concrete-like material outlined above is a constraint in ensuring that the roadway is safely supported apart from a portion thereof which is not sufficiently large as to be susceptible to breakage by forces exerted by neighbouring rock strata.
In order to achieve the required hardening rate a first slurry containing cement is added to a second slurry containing an agent for accelerating hardening of cement, the agent suitably being suspended in sodium bentonite as will be described subsequently in connection with Figure 2.
The suitability of an accelerating agent for use in the application outlined above and described in more detail subsequently is determined by testing as the agent must satisfy the parameters set out below.
The accelerating agent must meet stringent requirements before being allowed underground. For example, the agent must not be inflammable; it must have non-toxic combustion products, it must not be explosive or toxic itself or in combination with other materials employed underground.
Moreover the accelerating agent must not react with sodium bentonite so as to affect its gel properties to remove effective pumpability of the second slurry and of course the agent must accelerate the hardening of cement to the desired degree.
The following substances were tested inter alia for suitability as constituents of an agent for accelerating hardening of cement; (a) anhydrous sodium silicate or fluorosilicate, (b) aluminium chloride, (c) sodium hydroxide, (d) lithium carbonate, (e) ferrous or ferric nitrate, (f) a mixture of triethanolamine, sodium
carbonate and potassium carbonate, (g) mixtures of acetic acid or its salts and
triethanolamine.
It was found that substance (a) was an irritant to operators and also that it slowly solidified slurries of sodium bentonite to which it was added and was therefore not suitable. Substance (b) causes a rapid hardening of cement but reacts dangerously exbthermically and also destroys the gel structure of sodium bentonite and in consequence is also unsatisfactory. Substance (c), although an accelerator is unsuitable because it is highly caustic and destroys the gel properties of sodium bentonite. Substance (d) is a good accelerating agent and also does not affect the gel properties of sodium bentonite, but unfortunately it can exhibit hallucinogenic effects so that care would be required if using it. Substance (e) is suitable except that upon heating it releases toxic oxides of nitrogen and so cannot be used.
Substance (f) was suitable. Substance (g) is a very effective cement accelerator when used in controlled conditions. However in an uncontrolled mine environment, too much accelerator might be used and testing showed that this would cause the early strength of the concrete-like material to be severely reduced.
In view of the foregoing triethanolamine, sodium carbonate and potassium carbonate comprise the preferred accelerating agent for accelerating hardening of cement.
The testing indicated the quantity of alkali metal carbonate when added to the triethanolamine increased the early and later strength of the ordinary Portland cement. Several blends of agent of type (f) accelerating the hardening of ordinary Portland cement were tested with the following grout: 1000 parts coal fines up to half inch in size
400 parts of a 15:1 ratio of water to
bentonite
250 parts of ordinary Portland cement and
150 parts of water.
A representative four agents A, B, C and D of those tested are given overleaf as a percentage by weight of the cement in the above grout.
A. 7% sodium carbonate, 0.25% triethanol
amine
B. 2% sodium carbonate, 5% triethanol
amine
C. 7% sodium carbonate, and
D. 5% sodium carbonate, 1% potassium
carbonate and 1.5% triethanolamine.
The results of the four tests are given below in terms of uniaxial crushing strength after four hours and after twenty four hours:
4 Hours 24 Hours
A 28 kNm-2 1210 kNm-2 B 35' kNm 50 kNm-2 C 20 kNm 193 kNm D 72 kNm-2 248 kNm From the above tests, it can be seen that a high concentration of alkali metal carbonate gives a high later strength and a high concentration of triethanolamine gives a relatively high early strength.
As has been mentioned, triethanolamine does not affect the gel properties of sodium bentonite in the grout and testing shows that the alkali metal carbonates do not affect the gel properties to a degree sufficient to impair pumpability of slurries including bentonite, provided that sodium bentonite is pre-wetted.
Testing of the relative effectiveness of sodium and potassium carbonate is effected in the following manner. An agent comprising 5% triethanolamine and 2% sodium carbonate when used with a 0.8 water to cement ratio by weight of cement paste gives an initial set in 85 minutes and a final set of 115 minutes. An agent comprising 5% triethanolamine and 2% potassium carbonate gives an initial set in 41 minutes and a final set in 58 minutes. The testing is performed with a vicat apparatus.
Although potassium carbonate is more effective than sodium carbonate.at attaining early strength, the latter is preferred in the larger quantity because it is less caustic.
From performance testing and from price considerations a composition of agent which has tended to be most effective is by weight one and a half parts triethanolamine, five parts sodium carbonate and one part potassium carbonate. (i.e. D. above). The preferred agent is prepared by being crystallised out from aqueous solution.
This constitution of agent represents a compromise between fast setting and high strength at one day, which is particularly suitable for accelerating ordinary Portland cement used in coal mines.
Referring now to Figure 1 a performance graph is shown with compressive strength in
Megapascals plotted as ordinate and age in hours as abscissa. Four curves,1, 2, 3 and 4 are shown on the graph each representing a mix comprising ordinary Portland cement and a different quantity of accelerator the quantities being in the case of curve 1, 3.75% by weight of cement; in the case of curve 2, 7.5% by weight of cement; in the case of curve 3, 11.25% by weight of cement and in the case of curve 4, 15% by weight of cement.
A study of the graph of Figure 1 shows that the mix of curve 2 gives a similar compressive strength to the mixes of curves 3 and 4 after about 4 hours despite less agent being used.
Consequently, the ratio of agent to cement which is preferred is that of curve 2 i.e. three parts by weight of agent to forty parts by weight of ordinary Portland cement.
In practice, the quantity of agent added to the second slurry is governed by the type of cement which it will have to accelerate, the type and quality of dirt aggregate in the slurry and the quantity of water therein. These latter may vary considerably, because for example a band of dirt may have existed in the coal seam mined, thereby increasing the quantity of dirt in the aggregate. Consequently, it is found that the ratio by weight of accelerator can vary between about one and eight parts in forty parts of cement in the slurry. Nonetheless, the above mentioned figure of 7.5% (i.e.
three parts in forty) represents the desired proportion.
Turning now to Figure 2, formation of the concrete-like material shown at 1, is described in more detail. The concrete-like material is formed in situ in a cavity 12, defined by shuttering, which cavity can comprise a mine packhole arranged adjacent to a mine roadway (not shown). As the coal face advances, a succession of packholes is formed one after the other as new roadway is formed. Two pipes indicated at 14 and 15 respectively are adapted to feed into the packhole 12 via a mixing means 16. The first slurry comprising a mixture of cement and water is pumped through the pipe 14 by a pump 17. The first slurry is added to the pipe at a point generally indicated at F.The second slurry comprising a suspension of dirt aggregate, e.g. run-of-mine coal or pit waste and an agent for accelerating hardening of cement both suspended in sodium bentonite is pumped through the pipe 15 by a pump 18. The second slurry is added to the pipe 15 at a point generally indicated at G.
The first slurry does not set quickly so that after passage thereof through the pipe 14 has been effected, there is time for operators to wash out the pipe. The second slurry does not set at all since it comprises a dirt aggregate and the agent for hardening cement suspended in bentonite. Consequently, there is little danger of the pipes being filled with set cement and thereby being damaged.
The mixing means 16, which is not shown in detail, is provided to ensure that as far as possible material added to the packhole 12 is of a homogeneous nature. Of course, the provision of mixing means 16 is not essential to the invention as spattering of the first and second slurries upon entry into the packhole causes sufficient mixing. The mixing means merely enhances the mixing caused by spattering.
Furthermore the first slurry does not act so quickly as to prevent addition thereto of the second slurry if supply of the latter is interrupted through operational difficulties.
However, when the second slurry and the first slurry are mixed together in the packhole, then the agent for accelerating hardening of the cement acts upon the cement.
Consequently the two slurries harden into the concrete-like material 11. The concrete-like material 11 attains sufficient strength to support the mine roadway within the prescribed time mentioned above.
The material of the present invention finds alternative application including the sealing off of mine roadways. In such an application the first and second slurries are added to a cavity defined by containing means such as boards, which containing means are positioned so as to block the mine roadway. When the boards are filled with the mixture, the mixture sets and thereby seals off the roadway.
From the above description it can be seen that the present invention mitigates the disadvantages found hitherto in supporting a mine roadway.
WHAT WE CLAIM IS:
1. A method of preparing a supportive concrete-like material for at least partially filling a cavity in an underground mine comprising adding a first aqueous slurry including hydraulic cement to the cavity and concurrently adding a second aqueous slurry including an agent for accelerating hardening of the cement and leaving the slurries to harden into a supportive concrete-like material in the cavity.
2. A method as claimed in claim 1, wherein the second slurry contains a dirt aggregate.
3. A method as claimed in claim 1, wherein the first slurry contains a dirt aggregate.
4. A method as claimed in claim 2 or 3, wherein the dirt aggregate comprises run-ofmine coal or pit waste.
5. A supportive concrete-like material for at least partially filling a cavity in an underground mine the supportive concrete-like material being formed within the cavity by combining together and hardening, a first aqueous slurry including hydraulic cement and a second aqueous slurry including an agent for accelerating hardening of the cement.
6. A supportive concrete-like material as claimed in claim 5, wherein the agent is a mixture of triethanolamine and one or both of sodium carbonate and potassium carbonate.
7. A supportive concrete-like material according to claim 6, wherein the agent is a mixture of by weight, one and a half parts of triethanolamine, five parts sodium carbonate and one part potassium carbonate.
8. A supportive concrete-like material as claimed in claim 6 or 7, wherein the agent is present in the ratio by weight of one to eight parts agent to forty parts cement.
9. A method according to claim 1 of preparing material substantially as hereinbefore described and as shown in the accompanying drawings.
10. A supportive concrete-like material according to claim 5, substantially as hereinbefore described.
**WARNING** end of DESC field may overlap start of CLMS **.
Claims (10)
1. A method of preparing a supportive concrete-like material for at least partially filling a cavity in an underground mine comprising adding a first aqueous slurry including hydraulic cement to the cavity and concurrently adding a second aqueous slurry including an agent for accelerating hardening of the cement and leaving the slurries to harden into a supportive concrete-like material in the cavity.
2. A method as claimed in claim 1, wherein the second slurry contains a dirt aggregate.
3. A method as claimed in claim 1, wherein the first slurry contains a dirt aggregate.
4. A method as claimed in claim 2 or 3, wherein the dirt aggregate comprises run-ofmine coal or pit waste.
5. A supportive concrete-like material for at least partially filling a cavity in an underground mine the supportive concrete-like material being formed within the cavity by combining together and hardening, a first aqueous slurry including hydraulic cement and a second aqueous slurry including an agent for accelerating hardening of the cement.
6. A supportive concrete-like material as claimed in claim 5, wherein the agent is a mixture of triethanolamine and one or both of sodium carbonate and potassium carbonate.
7. A supportive concrete-like material according to claim 6, wherein the agent is a mixture of by weight, one and a half parts of triethanolamine, five parts sodium carbonate and one part potassium carbonate.
8. A supportive concrete-like material as claimed in claim 6 or 7, wherein the agent is present in the ratio by weight of one to eight parts agent to forty parts cement.
9. A method according to claim 1 of preparing material substantially as hereinbefore described and as shown in the accompanying drawings.
10. A supportive concrete-like material according to claim 5, substantially as hereinbefore described.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB26327/79A GB1576943A (en) | 1978-05-09 | 1978-05-09 | Filling cavities underground |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB26327/79A GB1576943A (en) | 1978-05-09 | 1978-05-09 | Filling cavities underground |
Publications (1)
Publication Number | Publication Date |
---|---|
GB1576943A true GB1576943A (en) | 1980-10-15 |
Family
ID=10241926
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB26327/79A Expired GB1576943A (en) | 1978-05-09 | 1978-05-09 | Filling cavities underground |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB1576943A (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE3322492A1 (en) * | 1982-06-24 | 1983-12-29 | Foseco International Ltd., Birmingham | CEMENT COMPOSITIONS AND METHOD FOR THE PRODUCTION THEREOF |
FR2589388A1 (en) * | 1985-11-01 | 1987-05-07 | Coal Industry Patents Ltd | PROCESS FOR THE PREPARATION AND USE OF A CURABLE CEMENT COMPOSITION COMPRISING COAL FINS |
-
1978
- 1978-05-09 GB GB26327/79A patent/GB1576943A/en not_active Expired
Cited By (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE3322492A1 (en) * | 1982-06-24 | 1983-12-29 | Foseco International Ltd., Birmingham | CEMENT COMPOSITIONS AND METHOD FOR THE PRODUCTION THEREOF |
FR2529192A1 (en) * | 1982-06-24 | 1983-12-30 | Foseco Int | CEMENT COMPOSITION BASED ON ALUMINA AND ANHYDRITE FOR THE PRODUCTION OF CURED CEMENT AND ADDITIVE THEREOF |
US4481037A (en) * | 1982-06-24 | 1984-11-06 | Fosroc International Limited | Cement compositions |
FR2589388A1 (en) * | 1985-11-01 | 1987-05-07 | Coal Industry Patents Ltd | PROCESS FOR THE PREPARATION AND USE OF A CURABLE CEMENT COMPOSITION COMPRISING COAL FINS |
GB2182323A (en) * | 1985-11-01 | 1987-05-13 | Coal Ind | Settable compositions |
US4770708A (en) * | 1985-11-01 | 1988-09-13 | Coal Industry (Patents) Limited | Method of disposing of mining tailings |
AU585662B2 (en) * | 1985-11-01 | 1989-06-22 | Coal Industry (Patents) Ltd. | Settable compositions and methods of use thereof |
GB2182323B (en) * | 1985-11-01 | 1989-10-25 | Coal Ind | Settable compositions and methods of use thereof |
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