AU2013206316A1 - Improved Low Energy Breaking Agent - Google Patents
Improved Low Energy Breaking Agent Download PDFInfo
- Publication number
- AU2013206316A1 AU2013206316A1 AU2013206316A AU2013206316A AU2013206316A1 AU 2013206316 A1 AU2013206316 A1 AU 2013206316A1 AU 2013206316 A AU2013206316 A AU 2013206316A AU 2013206316 A AU2013206316 A AU 2013206316A AU 2013206316 A1 AU2013206316 A1 AU 2013206316A1
- Authority
- AU
- Australia
- Prior art keywords
- breaking agent
- formulation
- detonator
- breaking
- agent
- 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.)
- Abandoned
Links
- 239000000203 mixture Substances 0.000 claims abstract description 87
- 239000003795 chemical substances by application Substances 0.000 claims abstract description 74
- 238000009472 formulation Methods 0.000 claims abstract description 70
- 239000002360 explosive Substances 0.000 claims abstract description 50
- 238000005474 detonation Methods 0.000 claims abstract description 44
- 239000011435 rock Substances 0.000 claims abstract description 28
- 230000035939 shock Effects 0.000 claims abstract description 25
- 230000000977 initiatory effect Effects 0.000 claims abstract description 9
- 239000000843 powder Substances 0.000 claims description 61
- 238000000034 method Methods 0.000 claims description 41
- 239000000446 fuel Substances 0.000 claims description 39
- 239000004411 aluminium Substances 0.000 claims description 24
- 229910052782 aluminium Inorganic materials 0.000 claims description 24
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 claims description 24
- 239000000020 Nitrocellulose Substances 0.000 claims description 20
- 241000269319 Squalius cephalus Species 0.000 claims description 20
- 229920001220 nitrocellulos Polymers 0.000 claims description 20
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 15
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 claims description 14
- 239000000295 fuel oil Substances 0.000 claims description 14
- 238000004078 waterproofing Methods 0.000 claims description 9
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 8
- 238000007514 turning Methods 0.000 claims description 8
- 239000003610 charcoal Substances 0.000 claims description 7
- 239000008187 granular material Substances 0.000 claims description 7
- 229910002804 graphite Inorganic materials 0.000 claims description 7
- 239000010439 graphite Substances 0.000 claims description 7
- 239000004922 lacquer Substances 0.000 claims description 7
- 238000002156 mixing Methods 0.000 claims description 7
- 229910000029 sodium carbonate Inorganic materials 0.000 claims description 7
- 238000004806 packaging method and process Methods 0.000 claims description 6
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical class [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 claims description 5
- 229940069428 antacid Drugs 0.000 claims description 5
- 239000003159 antacid agent Substances 0.000 claims description 5
- 230000001458 anti-acid effect Effects 0.000 claims description 5
- 239000002216 antistatic agent Substances 0.000 claims description 5
- 239000004615 ingredient Substances 0.000 claims description 5
- 239000004593 Epoxy Substances 0.000 claims description 4
- 239000005662 Paraffin oil Substances 0.000 claims description 4
- 229920002367 Polyisobutene Polymers 0.000 claims description 4
- 239000011230 binding agent Substances 0.000 claims description 4
- 239000012530 fluid Substances 0.000 claims description 4
- 229910001220 stainless steel Inorganic materials 0.000 claims description 4
- 239000010935 stainless steel Substances 0.000 claims description 4
- 238000002360 preparation method Methods 0.000 claims description 3
- 238000005507 spraying Methods 0.000 claims description 3
- 238000002309 gasification Methods 0.000 claims description 2
- 239000012188 paraffin wax Substances 0.000 claims description 2
- PAWQVTBBRAZDMG-UHFFFAOYSA-N 2-(3-bromo-2-fluorophenyl)acetic acid Chemical compound OC(=O)CC1=CC=CC(Br)=C1F PAWQVTBBRAZDMG-UHFFFAOYSA-N 0.000 description 12
- 239000000463 material Substances 0.000 description 12
- 239000007800 oxidant agent Substances 0.000 description 7
- 238000005422 blasting Methods 0.000 description 6
- 239000007789 gas Substances 0.000 description 6
- 238000004519 manufacturing process Methods 0.000 description 6
- FGIUAXJPYTZDNR-UHFFFAOYSA-N potassium nitrate Chemical compound [K+].[O-][N+]([O-])=O FGIUAXJPYTZDNR-UHFFFAOYSA-N 0.000 description 6
- 239000003721 gunpowder Substances 0.000 description 5
- VWDWKYIASSYTQR-UHFFFAOYSA-N sodium nitrate Chemical compound [Na+].[O-][N+]([O-])=O VWDWKYIASSYTQR-UHFFFAOYSA-N 0.000 description 5
- 239000011324 bead Substances 0.000 description 4
- 230000008901 benefit Effects 0.000 description 4
- 239000004794 expanded polystyrene Substances 0.000 description 4
- 239000003380 propellant Substances 0.000 description 4
- 244000007835 Cyamopsis tetragonoloba Species 0.000 description 3
- 239000002585 base Substances 0.000 description 3
- 238000004200 deflagration Methods 0.000 description 3
- 239000000839 emulsion Substances 0.000 description 3
- 235000010333 potassium nitrate Nutrition 0.000 description 3
- 239000004323 potassium nitrate Substances 0.000 description 3
- 235000010344 sodium nitrate Nutrition 0.000 description 3
- 239000004317 sodium nitrate Substances 0.000 description 3
- 239000004575 stone Substances 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 2
- 230000009471 action Effects 0.000 description 2
- 238000009412 basement excavation Methods 0.000 description 2
- 239000004202 carbamide Substances 0.000 description 2
- 238000010276 construction Methods 0.000 description 2
- 238000005336 cracking Methods 0.000 description 2
- YADSGOSSYOOKMP-UHFFFAOYSA-N dioxolead Chemical compound O=[Pb]=O YADSGOSSYOOKMP-UHFFFAOYSA-N 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 238000002474 experimental method Methods 0.000 description 2
- 238000004880 explosion Methods 0.000 description 2
- 238000013467 fragmentation Methods 0.000 description 2
- 238000006062 fragmentation reaction Methods 0.000 description 2
- 238000005065 mining Methods 0.000 description 2
- VLTRZXGMWDSKGL-UHFFFAOYSA-N perchloric acid Chemical class OCl(=O)(=O)=O VLTRZXGMWDSKGL-UHFFFAOYSA-N 0.000 description 2
- 239000004033 plastic Substances 0.000 description 2
- 229920005652 polyisobutylene succinic anhydride Polymers 0.000 description 2
- BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 2
- BAZAXWOYCMUHIX-UHFFFAOYSA-M sodium perchlorate Chemical compound [Na+].[O-]Cl(=O)(=O)=O BAZAXWOYCMUHIX-UHFFFAOYSA-M 0.000 description 2
- 229910001488 sodium perchlorate Inorganic materials 0.000 description 2
- IDCPFAYURAQKDZ-UHFFFAOYSA-N 1-nitroguanidine Chemical compound NC(=N)N[N+]([O-])=O IDCPFAYURAQKDZ-UHFFFAOYSA-N 0.000 description 1
- UHBVTTDRNVAOJD-UHFFFAOYSA-N 1-nitropropane-1,2,3-triol Chemical group OCC(O)C(O)[N+]([O-])=O UHBVTTDRNVAOJD-UHFFFAOYSA-N 0.000 description 1
- GDDNTTHUKVNJRA-UHFFFAOYSA-N 3-bromo-3,3-difluoroprop-1-ene Chemical compound FC(F)(Br)C=C GDDNTTHUKVNJRA-UHFFFAOYSA-N 0.000 description 1
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 1
- ZOXJGFHDIHLPTG-UHFFFAOYSA-N Boron Chemical compound [B] ZOXJGFHDIHLPTG-UHFFFAOYSA-N 0.000 description 1
- 244000303965 Cyamopsis psoralioides Species 0.000 description 1
- 229920002907 Guar gum Polymers 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
- 229910002651 NO3 Inorganic materials 0.000 description 1
- NHNBFGGVMKEFGY-UHFFFAOYSA-N Nitrate Chemical compound [O-][N+]([O-])=O NHNBFGGVMKEFGY-UHFFFAOYSA-N 0.000 description 1
- SNIOPGDIGTZGOP-UHFFFAOYSA-N Nitroglycerin Chemical compound [O-][N+](=O)OCC(O[N+]([O-])=O)CO[N+]([O-])=O SNIOPGDIGTZGOP-UHFFFAOYSA-N 0.000 description 1
- 239000004793 Polystyrene Substances 0.000 description 1
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 1
- 235000017899 Spathodea campanulata Nutrition 0.000 description 1
- 229910000831 Steel Inorganic materials 0.000 description 1
- FJWGYAHXMCUOOM-QHOUIDNNSA-N [(2s,3r,4s,5r,6r)-2-[(2r,3r,4s,5r,6s)-4,5-dinitrooxy-2-(nitrooxymethyl)-6-[(2r,3r,4s,5r,6s)-4,5,6-trinitrooxy-2-(nitrooxymethyl)oxan-3-yl]oxyoxan-3-yl]oxy-3,5-dinitrooxy-6-(nitrooxymethyl)oxan-4-yl] nitrate Chemical compound O([C@@H]1O[C@@H]([C@H]([C@H](O[N+]([O-])=O)[C@H]1O[N+]([O-])=O)O[C@H]1[C@@H]([C@@H](O[N+]([O-])=O)[C@H](O[N+]([O-])=O)[C@@H](CO[N+]([O-])=O)O1)O[N+]([O-])=O)CO[N+](=O)[O-])[C@@H]1[C@@H](CO[N+]([O-])=O)O[C@@H](O[N+]([O-])=O)[C@H](O[N+]([O-])=O)[C@H]1O[N+]([O-])=O FJWGYAHXMCUOOM-QHOUIDNNSA-N 0.000 description 1
- 229910052783 alkali metal Inorganic materials 0.000 description 1
- 229910001514 alkali metal chloride Inorganic materials 0.000 description 1
- 229910000272 alkali metal oxide Inorganic materials 0.000 description 1
- 150000001340 alkali metals Chemical class 0.000 description 1
- DVARTQFDIMZBAA-UHFFFAOYSA-O ammonium nitrate Chemical class [NH4+].[O-][N+]([O-])=O DVARTQFDIMZBAA-UHFFFAOYSA-O 0.000 description 1
- 150000001540 azides Chemical class 0.000 description 1
- 229910052796 boron Inorganic materials 0.000 description 1
- 239000013590 bulk material Substances 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 239000004568 cement Substances 0.000 description 1
- 150000001805 chlorine compounds Chemical class 0.000 description 1
- 239000000084 colloidal system Substances 0.000 description 1
- 238000002485 combustion reaction Methods 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 230000001934 delay Effects 0.000 description 1
- 230000003292 diminished effect Effects 0.000 description 1
- AXZAYXJCENRGIM-UHFFFAOYSA-J dipotassium;tetrabromoplatinum(2-) Chemical compound [K+].[K+].[Br-].[Br-].[Br-].[Br-].[Pt+2] AXZAYXJCENRGIM-UHFFFAOYSA-J 0.000 description 1
- 238000005553 drilling Methods 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 229960003711 glyceryl trinitrate Drugs 0.000 description 1
- 239000000665 guar gum Substances 0.000 description 1
- 229960002154 guar gum Drugs 0.000 description 1
- 235000010417 guar gum Nutrition 0.000 description 1
- 235000010299 hexamethylene tetramine Nutrition 0.000 description 1
- 239000004312 hexamethylene tetramine Substances 0.000 description 1
- VKYKSIONXSXAKP-UHFFFAOYSA-N hexamethylenetetramine Chemical compound C1N(C2)CN3CN1CN2C3 VKYKSIONXSXAKP-UHFFFAOYSA-N 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 239000003921 oil Substances 0.000 description 1
- 238000012856 packing Methods 0.000 description 1
- 238000000059 patterning Methods 0.000 description 1
- VLTRZXGMWDSKGL-UHFFFAOYSA-M perchlorate Inorganic materials [O-]Cl(=O)(=O)=O VLTRZXGMWDSKGL-UHFFFAOYSA-M 0.000 description 1
- 239000002985 plastic film Substances 0.000 description 1
- 229920006255 plastic film Polymers 0.000 description 1
- 239000011092 plastic-coated paper Substances 0.000 description 1
- 229920002223 polystyrene Polymers 0.000 description 1
- 229910000027 potassium carbonate Inorganic materials 0.000 description 1
- VKJKEPKFPUWCAS-UHFFFAOYSA-M potassium chlorate Chemical compound [K+].[O-]Cl(=O)=O VKJKEPKFPUWCAS-UHFFFAOYSA-M 0.000 description 1
- 229910001487 potassium perchlorate Inorganic materials 0.000 description 1
- 230000008569 process Effects 0.000 description 1
- 238000012163 sequencing technique Methods 0.000 description 1
- 229910052710 silicon Inorganic materials 0.000 description 1
- 239000010703 silicon Substances 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 239000010959 steel Substances 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
Landscapes
- Drilling And Exploitation, And Mining Machines And Methods (AREA)
Abstract
- 38 A breaking agent for use in boreholes and other rock or concrete breaking operations; said breaking agent operable with commercial detonating systems; said breaking agent 5 comprising a cartridged or poured volume of an explosive formulation, so formulated as to maintain a low velocity detonation in conditions of borehole confinement; velocity of said detonation being between 1200 and 2000 metres per second; characterised in that initiation of said low 10 velocity detonation of one, or an interconnected series, or a poured column of said breaking agent, may be initiated by any one of, an electric detonator, a shock tube detonator or an electronic detonator. p13 Signal tube or lead-wires r g t -. B h . Br h. e - -. ........... . .. .. .. . .. ... .... ......i
Description
P/00/009 Regulation 3.2 AUSTRALIA Patents Act 1990 COMPLETE SPECIFICATION Invention Title: IMPROVED LOW ENERGY BREAKING AGENT The invention is described in the following statement, including the best method of performing it known to us: Our Ref: aj - - 2 IMPROVED LOW ENERGY BREAKING AGENT This invention relates to improvements in rock and concrete breaking and has particular but not exclusive application for excavation, mining, construction and 5 demolition industries. BACKGROUND Conventional high explosive when placed in a borehole in rock or concrete and initiated by a commercial 10 detonator, will detonate, producing a strong shock wave, shattering the rock or concrete in close proximity to the borehole, blasting high speed, shocked gas through cracks and micro-cracks radiating axially from the near borehole shattered zone, and breaking and throwing rock or concrete 15 with great violence from the blast site. The detonation of conventional high explosive in a borehole drilled into rock or concrete shatters the surrounding rock or concrete and supersonic gas from the detonation propagates through cracks emanating from the 20 shattered zone of material immediately surrounding the detonation. The rock or concrete material is broken and displaced by a combination of shock action and heave imparted by the expanding gasses produced by detonation. A conventional, detonating high explosive needs no 25 confinement to detonate, providing the initial shock stimulus is enough to initiate detonation, although - 3 confinement will generally increase detonation pressure and velocity. Examples of conventional, detonator sensitive high explosives are Dynamite, Detonator sensitive emulsion, Ammonium Nitrate/Fuel Oil (ANFO), T.N.T and Plastic 5 Explosive. There are many other commercial and military high explosives known in the art. A onventionally detonating high explosive in commercial use, will detonate at velocities generally between 2500 meters per second and 6200 meters per second, depending on column height, 10 diameter and confinement conditions. In contrast to the behaviour of a conventionally detonating high explosive as described above, an explosive formulated to undergo a very low velocity, low pressure detonation, will, when initiated, explode in confinement as 15 described above, but will generate a very weak, low order shock wave during the low velocity detonation process, breaking and displacing the rock or concrete material surrounding the stemmed borehole containing the explosive by expansion of the explosion gasses and crack propagation 20 induced by the hot, expanding gasses. There is little or no shattered zone around the bore hole, in contradistinction to the shattered zone produced by conventionally detonating explosives as a general rule. A weakly detonating material or, for the purposes of 25 this explanation, a low order detonating material will, when initiated unconfined in small diameters, usually not - 4 support detonation, needing confinement to properly explode, whereas a conventional high explosive, as above described, will usually detonate without confinement provided the initiation stimulus is powerful enough. 5 A low order detonating explosive may detonate at speeds between 1200 and 2000 meters per second, compared to the higher velocities of conventionally detonating explosives in common commercial use. It is well known in the explosives art to lower the 10 detonation velocity of, for example, ammonium nitrate fuel oil mixtures (ANFO) by admixing, for example, expanded polystyrene beads with the prilled ANFO. This explosive is known as ANFOPS (Ammonium Nitrate Fuel Oil Polystyrene) . By Way of example an Orica product " Amex LD " has three 15 grades of ANFOPS, the 50 ANFO/50 Expanded Polystyrene Beads mix is quoted as detonating at between 2300 to 4000 meters per second, the 40 ANFO/60 Expanded Polystyrene Beads mix as detonating between 2100 and 3300 meters per second, and the 30 ANFO / 70 expanded Polystyrene Beads mix at between 20 2000 and 2900 meters per second. A minimum diameter for free poured Amex LD to detonate reliably is quoted as being 75 mm. ANFOPS requires a booster (a secondary, high velocity charge attached to a detonator which provides a very much 25 more powerful shock impulse necessary to detonate many - 5 commercial ammonium nitrate based commercial bulk explosives). In contradistinction, ANFO alone may detonate at between 2500 and 4800 meters per second (with a booster 5 attached to the detonator providing adequate shock stimulus) depending on borehole diameter and column height and confinement conditions. A non detonating, deflagrating explosive has uses when vibration is an issue or excessive fly rock is a 10 possibility. Deflagrating explosives, such as black powder or smokeless powder are usually described by those skilled in the art as having explosion velocities of below 1000 meters/second under severe confinement, although some very high velocity deflagrations can resemble low speed 15 detonations in effect. As deflagrating explosives produce little or no shock wave, they impart reduced vibration to surrounding rock strata. This diminished vibration can be very important in inner city construction sites or near critical infrastructure for example, where excessive 20 vibration can damage surrounding properties or equipment. Another use of non detonating explosives is the production of dimensional stone. A low velocity non detonating explosive will enable the operator to win large 25 unfractured blocks of dimensional stone without cracking or micro-cracking of the valuable rock.
- 6 It is known in the art that certain deflagrating materials are capable of detonation under sufficient conditions of confinement and with sufficient shock 5 stimulus, for example those which are donated by a detonator. An example of such a material is smokeless powder, a common propellant used for the bullets and shells fired from rifles, handguns and shotguns. Smokeless powder is composed of nitrocellulose, 10 combined with stabilisers and anti static agents, and provided as small flakes or grains. This type of smokeless powder is called Single Base powder. Another common smokeless powder is called Double Base powder, and contains a proportion of nitro-glycerine as well as nitrocellulose. 15 The nitrocellulose and nitro-glycerine form a solid colloid when combined which is safe to handle and use. Both types of powder do not detonate when used correctly for their intended purpose, that is, propulsion of projectiles from gun, rifle or handgun barrels. 20 Rather it is the case that these smokeless powders undergo a very fast, controlled burn, thus propelling the bullet or shot at a controllable velocity. If either type of powder was to detonate in a gun barrel, the results would be catastrophic, as the shock wave generated would 25 shatter the breech of the weapon, probably killing or injuring the firer. The reason this does not happen is that -7 the powder is ignited by a spit of flame from the cartridge or shot shell primer, and proceeds to burn, under the conditions of confinement existing within the breech and barrel, in a highly controllable and extremely rapid 5 manner. However it is also the case that both types of smokeless powder can be induced to detonate, given sufficient conditions of confinement and an adequate shock input, for example that provided by a commercial detonator, 10 or detonator booster assembly, particularly in the case of double base smokeless powders. By further way of example, there have been a number of bombing incidents where smokeless powder has been used as a high explosive. The Atlantic City bombing during the 15 Olympics of 1996 was one such. It is well known in the art that if a cartridge containing smokeless powder is placed into a borehole in rock or concrete, primed with a commercial detonator and well stemmed, the powder may detonate. This means that 20 smokeless powder can perfectly well be used as a high explosive if initiated with a commercial detonator or booster. If the same assembly is provided with an igniter, rather than a detonator, the confined smokeless powder will 25 burn rapidly under confinement, thus breaking the rock in a non detonating manner as above described. An igniter is usually an electric igniter or a shock tube igniter that generates a hot flame and sparks, well known to those skilled in the art. Igniters may contain, among many other compounds, lead 5 mono nitro resorcinate, potassium chlorate, boron, lead dioxide, silicon. All being, in various combinations, igniferous and formulated to produce a hot flame and/or copious sparks. In contrast with an igniter, a detonator contains a 10 high explosive such as penta erythrytol tetranitrate, as well as a primary explosive such as lead azide and, when functioned, detonates, producing an intense localized shock wave, sufficient to detonate most substances capable of detonation. 15 US Patent 5765923 describes the use of the above described nitrocellulose based propellant powder in a rock or concrete breaking role; the powder is ignited rather than detonated. US application 2003/0015112 describes a deflagrating 20 composition that may be composed of "a group consisting of nitrocellulose, nitroguanidine, sodium nitrate, ammonium nitrate and mixtures thereof" or "any suitable energetic material that deflagrates" housed in a cartridge and ignited by "a high energy igniter", and that this 25 composition has a "burn rate ranging from about 100 to about 400mm/sec".
- 9 US application 2005/0132921 describes "propellant coated with ammonium nitrate" as a deflagrating composition for use in rock breaking. All the above cited patents claim deflagrating 5 compositions ignited by an igniter. A disadvantage of igniters is that it is usually electrically initiated, and must be affixed to the cartridge containing the above described propellant in a manner that is secure and completely waterproof. 10 A disadvantage of this system is that the above -described electric igniters are instantaneous in action; each cartridge must be provided with an igniter, and there may be many cartridges required in any one rock or concrete breaking shot, and the cartridges are not interconnectable. 15 The operator therefore has to connect in series all the lead wires appending from the igniters embedded in the cartridges, wherever the cartridges may be in a series of boreholes. This leads to very complicated wiring procedures and frequently results in misfires. Because all the shots 20 must be fired instantaneously the operator cannot avail himself of the wide range of delay shock tube and electronic detonators available from commercial explosives suppliers. Another disadvantage of this product is that the 25 deflagration of the smokeless powder, or other deflagrating compositions, under conditions of cartridge in borehole - 10 confinement is so slow that, unless all holes are fired practically simultaneously, flaming combustion products vent from cracks developed by other fired holes, thus wasting the energy developed by the smokeless powder, or 5 other deflagrating composition, leading to poor breakage. This means frequently sub optimal breakage patterns are common due to the lack of ability to control fragmentation through the skilled use of delays between explosive events. 10 Vibration can also become a problem due to the necessity to fire all the charges in a round simultaneously. Even if the charges are not detonating, the sheer mass of rock or concrete being moved can impart unacceptable vibration levels to a critical site. 15 There exist electro-mechanical or electronic delay systems for instantaneous igniters but they are complicated and very expensive. These types of delay systems are more usually encountered in the fireworks display industry, where precise timing of individual firework shots is 20 critical. They are not suited to routine excavation and demolition operations. It is an aim of the current invention to provide a system for those engaged in drilling and blasting rock or concrete that is amenable to the use of commercial 25 detonating systems, for example Orica Exceldet products.
- 11 Currently commercial non-detonating breaking agents must rely on the use of an igniter to initiate deflagration. It is known in the art that gunpowder (black powder) is an explosive that is a reliable deflagrant, will not 5 detonate, and has been used for centuries as a blasting explosive. It has long been supplanted by high explosives for most rock breaking tasks, but is still used for production of dimensional stone, particularly in Italy. A disadvantage of black powder is that it is not very 10 powerful (about a fifth as powerful as ammonium nitrate/fuel oil, as above described) and does not produce much gas compared to other explosive materials. Another disadvantage is that it is also extremely sensitive to flame, sparks and friction, and will explode with a very 15 hot fireball unconfined. It is regarded worldwide as an extremely dangerous substance, with good reason. It is an object of the current invention to address or at least ameliorate the above mentioned disadvantages of 20 the above described contemporary commercial products. Notes 1. The term "comprising" (and grammatical variations thereof) is used in this specification in the inclusive sense of "having" or "including", and not in the 25 exclusive sense of "consisting only of".
- 12 2. The above discussion of the prior art in the Background of the invention, is not an admission that any information discussed therein is citable prior art or part of the common general knowledge of persons skilled 5 in the art in any country. BRIEF DESCRIPTION OF INVENTION In a first broad form of the invention there is provided a formulation of an oxidiser in prill form in combination with an effective amount of gasifier or fuel; the 10 formulation when activated adapted to deflagrate. Preferably, said prill is provided in granules in diameters ranging between 0.25mmm and 3.5mm. Preferably, said prill is provided in granules in diameters ranging between 1mm and 3mm. 15 Preferably, said prill acts as a fuel or gassifier. Preferably, said formulation further including a graphite or charcoal powder; said graphite or charcoal powder acting as a fuel and an antistatic agent. Preferably, said formulation further including an aluminium 20 powder; said aluminium powder acting as a fuel. Preferably, said formulation further including aluminium fine turnings or aluminium swarf; said aluminium fine turnings or aluminium swarf acting as a fuel.
- 13 Preferably, said formulation further including a sodium carbonate; said sodium carbonate acting as an antacid. Preferably, said formulation further including a nitrocellulose; said nitrocellulose acting as a fuel. 5 Preferably, said nitrocellulose acts as waterproofing agent. Preferably, said formulation further including a Guar Gum; said Guar Gum acting as fuel. Preferably, Guar Gum acts as a waterproofing agent and 10 binder. Preferably, said formulation further including water; said water acting as a working fluid enabling binding and Guar Gum gelling. In a further broad form of the invention there is provided 15 a method for the preparation of the formulation described above; said method including the steps of: (a) adding ingredients one by one or part premixed to an epoxy coated or stainless steel mixing drum or ribbon blender. 20 (b) spraying in nitrocellulose lacquer and/or water, (c) letting the product dry by air circulation during rotation of the drum.
- 14 Preferably, said method includes the further step of packaging said formulation into cartridges. Preferably, said method includes the further step of packaging said formulation into chubs. 5 Preferably, said method includes the further step of transferring said formulation into bulk carrier dispenser units by means of an auger. In still a further broad form of the invention there is provided a method of applying a low energy breaking agent 10 to a bore hole; said method including the steps of: (a) providing a formulation according to the formulation described above in at least one cartridge, (b) providing said at least one cartridge with a 15 detonator or igniter at one end of said cartridge, (c) lowering said at least one cartridge with detonator end first to the bottom of said bore hole, 20 (d) Stemming an area of said bore hole above said at least one cartridge.
- 15 In a further broad form of the invention there is provided a method of applying a low energy breaking agent to a bore hole; said method including the steps of: (a) providing a formulation according to the 5 formulation described above in the form of a chub, (b) providing said chub with a detonator or igniter at one end of said chub, (c) lowering said chub with detonator end first to 10 the bottom of said bore hole, (d) Stemming an area of said bore hole above said at least one cartridge. In a further broad form of the invention there is provided a method of applying a low energy breaking agent to a bore 15 hole; said method including the steps of: (a) Lowering a igniferous primer with a detonator or igniter into said bore hole, (b) pouring a formulation according to any one of claims 1 to 14 into said bore hole, 20 (c) Stemming an upper portion of said bore hole. In a further broad form of the invention, there is provided a breaking agent for use in boreholes and other - 16 rock or concrete breaking operations; said breaking agent operable with commercial detonating systems; said breaking agent comprising a cartridged or poured volume of an explosive formulation, so formulated as to maintain 5 a low velocity detonation in conditions of borehole confinement; velocity of said detonation being between 1200 and 2000 metres per second; characterised in that initiation of said low velocity detonation of one, or an interconnected series, or a poured column of said 10 breaking agent, may be initiated by any one of, an electric detonator, a shock tube detonator or an electronic detonator. Preferably, said formulation includes one or more oxidisers in powder or prill form in combination with an 15 effective amount of gasification or fuel; said formulation when activated adapted to said low velocity detonation. Preferably, said powder or prill is provided in granules in diameters ranging between 0.001mm and 3.5mm. 20 Preferably, said powder or prill is provided in granules in diameters ranging between 0.001 and 3mm. Preferably, said powder or prill acts as a fuel or gasifier.
- 17 Preferably, said formulation further includes fuel oil or paraffin as a fuel. Preferably, said formulation further includes a graphite or charcoal powder; said graphite or charcoal powder 5 acting as a fuel and an antistatic agent. Preferably, said formulation further includes an aluminium powder; said aluminium powder acting as a fuel. Preferably, said formulation further includes aluminium fine turnings or aluminium swarf; said aluminium fine 10 turnings or aluminium swarf acting as a fuel. Preferably, said formulation further includes a sodium carbonate; said sodium carbonate acting as an antacid. Preferably, said formulation further includes a nitrocellulose; said nitrocellulose acting as a fuel. 15 Preferably, said nitrocellulose acts as waterproofing agent. Preferably, said breaking agent further includes fuel oil, preferably diesoline. Preferably, said breaking agent further includes fuel 20 oil, preferably paraffin oil. Preferably, said breaking agent further including polyisobutylene.
- 18 Preferably, said breaking agent further includes a Guar Gum; said Guar Gum acting as fuel. Preferably, said Guar Gum acts as a waterproofing agent and binder. 5 preferably, said breaking agent further including water; said water acting as a working fluid enabling binding and Guar Gum gelling. In still a further broad form of the invention, there is provided a method for the preparation of the breaking 10 agent of any one of claims 1 to 13; said method including the steps of: (a) adding ingredients one by one or part premixed to an epoxy coated or stainless steel mixing drumor ribbon blender, 15 (b) spraying in nitrocellulose lacquer and/or water, (c) letting the product dry by air circulation during rotation of the drum. Preferably, said method includes the further step of 20 packaging said breaking agent into cartridges. Preferably, said method includes the further step of packaging said breaking agent into chubs.
- 19 Preferably, said method includes the further step of transferring said breaking agent into bulk carrier dispenser units by means of an auger. In another broad form of the invention, there is provided 5 a method of applying a low energy breaking agent to a bore hole; said method including the steps of: (a) providing a formulation according to any one of claims 1 to 14 in at least one cartridge, (b) providing said at least one cartridge with a 10 detonator at one end of said cartridge, (c) lowering said at least one cartridge with detonator end first to the bottom of said bore hole, (d) Stemming an area of said bore hole above said 15 at least one cartridge. In yet a further broad form of the invention, there is provided a method of applying a low energy breaking agent to a bore hole; said method including the steps of: (a) providing a formulation according to any one of 20 claims 1 to 14 in the form of a chub, (b) providing said chub with a detonator at one end of said chub, - 20 (c) lowering said chub with detonator end first to the bottom of said bore hole, (d) stemming an area of said bore hole above said at least one cartridge. 5 In one more broad form of the invention, there is provided a method of applying a low energy breaking agent to a bore hole; said method including the steps of: (a) lowering a detonator into said bore hole, (b) pouring a formulation according to any one of 10 claims 1 to 14 into said bore hole, (c) stemming an upper portion of said bore hole. 15 BRIEF DESCRIPTION OF DRAWINGS Embodiments of the present invention will now be described with reference to the accompanying drawings wherein: Figure 1 is a cross section of an area of strata and a 20 bore hole showing a first preferred embodiment of the invention using a cartridge form of the breaking agent, Figure 2 is a cross section of an area of strata and a bore hole showing a second preferred embodiment of the invention using a chub form of the breaking agent, - 21 Figure 3 is a cross section of a an area of strata and a bore hole showing a third preferred embodiment of the invention using a loose poured form of the breaking agent. 5 DETAILED DESCRIPTION OF PREFERRED EMBODIMENTS The present invention comprises a cartridged or bulk series of formulations for the explosive breaking of rock or concrete that, when exposed to the shock of the detonation of a commercial detonator, will detonate only at 10 a very low detonation pressure and velocity in the range of 1200 to 1900 meters per second, generating a very weak shock wave through the material to be blasted, not shattering rock or concrete in close proximity to the borehole, but generating gas at high temperature and 15 pressure to aid break up, heave and throw of the rock or concrete. The present invention is of particular utility for blasting tasks requiring a very low level of vibration so as to protect critical infrastructure, property and 20 structures in close proximity to the blast. The invention comprises a cartridged or bulk explosive, each cartridge being able to be connected to the other, and a commercial electric, shock tube or electronic detonator which can be inserted into in each cartridge. The 25 cartridges may be conveniently fashioned from waxed or plastic coated paper or plastic film, and tamped together - 22 in a borehole, much the same way as for ordinary commercial packaged high explosives, such as dynamite or cap sensitive emulsion. 5 The bulk material can be poured directly into a borehole and initiated with a commercial detonator. Turning now to the drawings, with reference to Figure 1, the breaking agent formulation described above may, in a first preferred embodiment, be encapsulated in suitable 10 packing to form cartridges 12. One or more cartridges 12 interconnected by a joiner 14 are lowered into a pre drilled bore-hole 16 in strata 10. A detonator 18 is located at the lower end of the lower cartridge with a signal tube or lead wires 20 exiting the bore-hole and 15 connected to some suitable detonation point (not shown) . The bore-hole is then provided with stemming material 22 and the low velocity detonation initiated. In a second preferred embodiment of the invention with 20 reference to Figure 2, the formulation is formed as a chub or cartridge 112. The chub or cartridge is likewise provided with a detonator 118 at its lower end and a signal tube or lead wires 120 led from the bore-hole to a detonation point. 25 In a third preferred embodiment with reference to Figure 3, a low velocity detonating formulation as - 23 described above, may be poured as a loose mixture 212 into a bore hole 216, after first lowering a correctly oriented detonator 218 to the bottom of the bore hole. Again the upper portion of the bore-hole is filled with a suitable 5 stemming 222. The advantages of the breaking agent of the present invention over any other non detonating or detonating products in use currently, is that the operator can treat the low detonation velocity between 1200 and 2000 metres 10 per second, low detonation pressure cartridged product exactly the same as a cartridged high explosive like dynamite. Likewise, the bulk product can be treated in much the same way as a bulk, pourable high explosive like Ammonium 15 Nitrate/Fuel Oil (the most commonly used commercial explosive in the world), and users can fully avail themselves of the advantages offered by modern detonating systems, while retaining the advantages of using a low power explosive to drastically reduce vibration and throw 20 when compared to a conventional high explosive. This means better rock or concrete breakage due to more control over the sequencing of shots and also greatly reduced vibration by virtue of the low order detonation nature of the novel explosive. 25 The current invention is safer and more powerful than gunpowder and similar deflagrants, has very reduced - 24 shattering effect in comparison to conventional high explosives. Furthermore, it burns with difficulty, is extremely insensitive to external stimuli such as friction and impact, only detonates when supplied with stimulus from 5 a commercial detonator. As well, it produces more than adequate amounts of gas for efficient breaking of rock or concrete, and may be contained in easy to use, easy to link together cartridges or as a bulk poured material. It can also be initiated to low velocity detonation of 10 between 1200 and 2000 meters per second by any commercial detonating system, offering great advantage to the skilled shot-firer who can minimize vibration and maximize breakage by skilled use of modern mining delay products such as shock tube and electronic delay detonators and shot plan 15 computer programmes. This is in contrast to existing deflagrating products that only offer instantaneous, fixed, ignition, with no possibility of efficient delay patterning and extremely cumbersome, time consuming and inefficient wiring up procedures. 20 The Formulation The general formulation components of the novel explosive and their functions are as follows; * Ammonium Nitrate powder or prill (oxidizer), * Sodium Nitrate powder or prill (oxidizer), 25 * Potassium Nitrate powder or prill (oxidizer), - 25 * Potassium Perchlorate powder or prill (oxidizer), " Sodium Perchlorate powder or prill (oxidizer), e Ammonium Perchlorate powder or prill (oxidizer), * Gunpowder (black powder) granular (ignition aid), 5 * Fuel Oil, Paraffin Oil, Polyisobutylene, * Urea powder or prill (fuel, gassifier), * Hexamine powder or prill (fuel, gassifier), * Graphite or charcoal powder (fuel, antistatic agent), * Aluminium Powder (fuel), 10 * Aluminium fine turnings or swarf (fuel), * Sodium Carbonate powder (antacid), * Potassium Carbonate (antacid), * Nitrocellulose lacquer (fuel and waterproofing agent), * Guar Gum (fuel ,waterproofing agent and binder), 15 e Water (working fluid enabling binding and guar gelling) Preferably *the formulation may further include a surfactant such as PIBSA (poly isobutylene succinic anhydride) dissolved in the above fuel or paraffin oil, 20 with the Polyisobutylene acts as a water proofing agent and fuel. The specific formulations may vary according to job requirements, as some components can be interchanged for various purposes, such as bulk loading into a borehole, use - 26 in wet boreholes, or small diameter cartridging for use in small diameter boreholes. A dry formulated formulation may be cartridged or bulk poured into a borehole. 5 The use of guar gum confers a degree of water resistance to the formulation mixtures, as does nitrocellulose lacquer, if the lacquer, with an evaporating solvent, is introduced to the dry mix during mixing operations. The addition of water to a formulation containing guar 10 gum can result in a rubbery gel or granules coated with a waterproof guar/water gel that can be either cartridged or provided as large diameter chubs or pumped directly into a borehole. In general, the ammonium nitrate content will be kept 15 below 60% if the formulation is to be initiated with a detonator. This is to prevent the tendency of Ammonium Nitrate (A.N) fuel mixtures to detonate at a relatively high velocity compared to the detonation velocity of the present invention, even if heavily diluted with other 20 substances when exposed to a severe shock from a commercial detonator or high explosive booster for example. The low A.N formulation will detonate with a low detonation velocity of between 1200 to 2000 metres per second depending on formulation with more than adequate generation 25 of the high pressure gasses to crack and heave rock or concrete.
- 27 The A.N will, along with the other oxidizers and fuels generally described above, undergo low velocity detonation as described above, with the attendant production of large quantities of gas, predominantly nitrogen, with carbon 5 dioxide and water vapour, as well as alkali metal oxides and chlorides. Generally, the ratio of alkali metal and ammonium nitrates, perchlorates and gunpowder will be between 60 and 95 percent of the total formulation mix, depending on 10 application, borehole diameter and method of initiation. The ratio of the "fuel" components will vary from between 40 to 5 percent depending on the conditions elucidated above. In all cases, the formulation will be blended to 15 promote low velocity detonation in large, medium or small diameter boreholes, The formulations will vary according to the job requirements. For example, a small diameter cartridged product formulation may have more A.N, Perchlorate, aluminium and 20 gunpowder in it than a medium or large diameter application, in which the ratio of AN will drop in relation to Sodium or Potassium Nitrate, and the fuel and gassifier content will be increased, because of the tendency of medium to large diameter masses of AN/fuel containing 25 formulations to transit from low velocity detonation to high order detonation and small diameters of AN/fuel - 28 formulations having difficulty detonating , especially when the AN is in prill form, and not finely divided. There is a limit to this tendency to low velocity detonation, probably around less than 30 percent AN, so the 5 formulation will be optimized for the conditions, preventing the A.N/fuel from transiting to high velocity detonation, that is, to above 2000 metres per second, and tailored for the formulation to undergo a low velocity detonation in conditions of borehole confinement. 10 Manufacture Manufacture is relatively simple, ingredients may simply be added one by one (or part premixed) to an epoxy coated or stainless steel cement mixer type, rotating open ended mixing drum, rotating the drum. Alternatively a 15 ribbon blender may be employed for mixing the ingredients. Either nitrocellulose lacquer or water or both may be sprayed in if required. After sufficient mixing, the product dry is allowed to dry by air circulation during rotation of the drum, and then packaged either in 20 cartridges, chubs or loaded by auger into bulk carrier dispenser units, in much the same way as into ANFO (ammonium nitrate/fuel oil) loading trucks. The present invention comprises a general formulation from which specific formulations can be derived, tailored 25 to detonate with low velocity of between 1200 to 2000 metres per second, rather than detonate with higher - 29 velocities above 2000 metres per second with detonator initiation in all desired circumstances, providing a valuable and flexible addition to safe and efficient blasting practice. 5 The particular formulation will very much depend on application; extensive trialing before commercial production will indicate what the best formulae are for given work conditions, so a body of specialist knowledge built up during the pre commercial stage will indicate what 10 specific formulations are best for specific job conditions. In Use It will be understood that the above described product will be offered to users with a linkable, joinable 15 cartridge system for use in small diameter boreholes, enabling one detonator to initiate an entire column of linked cartridges. The aim of this linkable cartridging system is to supply a product as much like a conventional high explosive product as possible, for example resembling 20 any one of a number of joinable or linkable cartridge systems as used by the seismic explosives industry. This functionality is in marked contrast to the above described existing commercial smokeless powder or other deflagrating composition containing cartridge system, each 25 cartridge with a separate instantaneous electric or shock tube detonator, which obliges the shot-firer to engage in - 30 complicated and misfire prone large series circuit hook-ups or instantaneous initiation of a large number of shock tube initiated units, sacrificing the ability to adequately delay between shots, and thus being unable to optimize 5 blasting practice. Experiments In experiments conducted by the inventors, cartridges of breaking agent according to the current invention, in diameters ranging from 25 to 40 mm and quantities up to 300 10 grams, were placed in varying levels of confinement. These included placement in conditions of mild confinement (plastic pipe), medium confinement (aluminium pipe) and severe confinement (steel pipe. All were reliably detonated at 1600 meters per second, plus or minus 100 meters per 15 second, with a commercial No8* detonator as shock stimulus. In contradistinction, crushed ANFO displayed a detonation velocity of 2750 meters per second in a diameter of 30 mm when confined in an aluminium pipe with a No8* detonator shock stimulus. 20 The exemplary formulation utilised in both the velocity determinations and in quarry trial were the following: Crushed ammonium nitrate - 58 Fuel Oil - 3.3 25 Crystalline potassium nitrate - 29 Urea prill - 6.5 - 31 Guar - 1.5 Coated aluminium powder - 3.7 Sodium perchlorate - 3.7 The inventors also conducted comparative trials of the 5 current invention in comparison with the above described deflagrating smokeless powder product in a sandstone quarry. Because the current invention enables the use of modern delay detonation systems, vibration was reduced and fragmentation was better. The "half barrels" left in the 10 free face after the shots, indicated that there was no shattering around the cartridge locations, in contradistinction to a conventional high explosive such as ANFO or a cartridged dynamite or emulsion. "Hooking Up", (the attachment, connection and running out of initiation 15 systems) was in all cases much faster and simpler in comparison to the deflagrating smokeless powder product, which relies on instantaneous electric igniters for initiation, necessitating a time consuming and complex "hook up". 20 The above describes only some embodiments of the present invention and modifications, obvious to those skilled in the art, can be made thereto without departing from the scope of the present invention. 25
Claims (25)
1. A breaking agent for use in boreholes and other rock or concrete breaking operations; said breaking agent operable with commercial detonating systems; said 5 breaking agent comprising a cartridged or poured volume of an explosive formulation, so formulated as to maintain a low velocity detonation in conditions of borehole confinement; velocity of said detonation being between 1200 and 2000 metres per second; 10 characterised in that initiation of said low velocity detonation of one, or an interconnected series, or a poured column of said breaking agent, may be initiated by any one of, an electric detonator, a shock tube detonator or an electronic detonator. 15
2. The breaking agent of claim 1 wherein said formulation includes one or more oxidisers in powder or prill form in combination with an effective amount of gasification or fuel; said formulation when activated adapted to said low velocity detonation. 20
3. The breaking agent of claim 2 wherein said powder or prill is provided in granules in diameters ranging between 0.001mm and 3.5mm. - 33
4. The breaking agent of claim 2 wherein said powder or prill is provided in granules in diameters ranging between 0.001 and 3mm.
5. The breaking agent of any one of claims 2 to 4 wherein 5 said powder or prill acts as a fuel or gasifier.
6 The breaking agent of any one of claims 1 to 5 wherein said formulation further includes fuel oil or paraffin as a fuel.
7. The breaking agent of any one of claims I to 6 wherein 10 said formulation further includes a graphite or charcoal powder; said graphite or charcoal powder acting as a fuel and an antistatic agent.
8. The breaking agent of any one of claims 1 to 7 wherein said formulation further includes an aluminium powder; 15 said aluminium powder acting as a fuel.
9. The breaking agent of any one of claims 1 to 8 wherein said formulation further includes aluminium fine turnings or aluminium swarf; said aluminium fine turnings or aluminium swarf acting as a fuel. 20
10. The breaking agent of any one of claims 1 to 9 wherein said formulation further includes a sodium carbonate; said sodium carbonate acting as an antacid. - 34
11. The breaking agent of any one of claims 1 to 10 wherein said formulation further includes a nitrocellulose; said nitrocellulose acting as a fuel.
12. The breaking agent of claim 11 wherein said 5 nitrocellulose acts as waterproofing agent.
13. The breaking agent of any one of claims 1 to 12 wherein said breaking agent further includes fuel oil, preferably diesoline.
14. The breaking agent of any one of claims 1 to 13 10 wherein said breaking agent further includes fuel oil, preferably paraffin oil.
15. The breaking agent of any one of -claims 1 to 14 wherein said breaking agent further including polyisobutylene. 15
16. The breaking agent of any one of claims 1 to 15 wherein said breaking agent further includes a Guar Gum; said Guar Gum acting as fuel.
17. The breaking agent of claim 16 wherein said Guar Gum acts as a waterproofing agent and binder. 20
18. The breaking agent of any one of claims I to 17 wherein said breaking agent further including water; said water acting as a working fluid enabling binding and Guar Gum gelling. - 35
19. A method for the preparation of the breaking agent of any one of claims 1 to 13; said method including the steps of: (a) adding ingredients one by one or part premixed 5 to an epoxy coated or stainless steel mixing drum or ribbon blender, (b) spraying in nitrocellulose lacquer and/or water, (c) letting the product dry by air circulation 10 during rotation of the drum.
20, The method of claim 19 wherein said method includes the further step of packaging said breaking agent into cartridges.
21. The method of claim 19 wherein said method 15 includes the further step of packaging said breaking agent into chubs.
22. The method of claim 19 wherein said method includes the further step of transferring said breaking agent into bulk carrier dispenser units by 20 means of an auger.
23. A method of applying a low energy breaking agent to a bore hole; said method including the steps of: - 36 (a) providing a formulation according to any one of claims 1 to 14 in at least one cartridge, (b) providing said at least one cartridge with a detonator at one end of said cartridge, 5 (c) lowering said at least one cartridge with detonator end first to the bottom of said bore hole, (d) Stemming an area of said bore hole above said at least one cartridge. 10
24. A method of applying a low energy breaking agent to a bore hole; said method including the steps of: (a) providing a formulation according to any one of claims 1 to 14 in the form of a chub, (b) providing said chub with a detonator at one end 15 of said chub, (c) lowering said chub with detonator end first to the bottom of said bore hole, (d) stemming an area of said bore hole above said at least one cartridge. 20
25. A method of applying a low energy breaking agent to a bore hole; said method including the steps of: - 37 (a) lowering a detonator into said bore hole, (b) pouring a formulation according to any one of claims 1 to 14 into said bore hole, (c) stemming an upper portion of said bore hole.
Priority Applications (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| AU2013206316A AU2013206316A1 (en) | 2007-05-28 | 2013-06-13 | Improved Low Energy Breaking Agent |
| AU2014203265A AU2014203265B2 (en) | 2007-05-28 | 2014-06-16 | Improved low energy breaking agent |
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| AU2007902823 | 2007-05-28 | ||
| AU2008202291A AU2008202291A1 (en) | 2007-05-28 | 2008-05-26 | Improved Low Energy Breaking Agent |
| AU2013206316A AU2013206316A1 (en) | 2007-05-28 | 2013-06-13 | Improved Low Energy Breaking Agent |
Related Parent Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| AU2008202291A Division AU2008202291A1 (en) | 2007-05-28 | 2008-05-26 | Improved Low Energy Breaking Agent |
Related Child Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| AU2014203265A Division AU2014203265B2 (en) | 2007-05-28 | 2014-06-16 | Improved low energy breaking agent |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| AU2013206316A1 true AU2013206316A1 (en) | 2013-07-04 |
Family
ID=48700189
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| AU2013206316A Abandoned AU2013206316A1 (en) | 2007-05-28 | 2013-06-13 | Improved Low Energy Breaking Agent |
Country Status (1)
| Country | Link |
|---|---|
| AU (1) | AU2013206316A1 (en) |
-
2013
- 2013-06-13 AU AU2013206316A patent/AU2013206316A1/en not_active Abandoned
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| Fordham | High explosives and propellants | |
| Zou | Explosives | |
| Meyer et al. | Explosives | |
| US3062147A (en) | Igniter for solid propellant grains | |
| Stoycheva et al. | Innovative formulations for a new generation of low-speed explosive compositions, designed for blasting in tender conditions and for extraction of rock-cladding materials | |
| CN101629795A (en) | Detonating of ignition booster device | |
| NO310349B1 (en) | Method of preventing sulfide dust explosions in connection with blasting | |
| AU2014203265B2 (en) | Improved low energy breaking agent | |
| AU2008202291A1 (en) | Improved Low Energy Breaking Agent | |
| CA1331935C (en) | Multi-directional initiator for explosives | |
| WO2000026603A1 (en) | Non-primary detonators | |
| US5608184A (en) | Alternative use of military propellants as novel blasting agents | |
| KR100508230B1 (en) | Cast explosive composition with microballoons | |
| AU2013206316A1 (en) | Improved Low Energy Breaking Agent | |
| CA3031356A1 (en) | A method of and a cartridge for disarming an unexploded blasting charge in a drill hole | |
| Naik et al. | High energy materials: A brief history and chemistry of fireworks and rocketry | |
| CA2252353C (en) | Non-primary detonator | |
| Lee | Explosives development and fundamentals of explosives technology | |
| Yusof et al. | PREDICTION OF AIR BLAST PRESSURE FOR MILITARY AND COMMERCIAL EXPLOSIVE USING ANSYS AUTODYN. | |
| Todd | Energetic Materials Fundamentals and Applications. | |
| Cranney et al. | Chemical explosives | |
| Shishkov et al. | Rock splitting with pyrotechnic compositions and secondary propellants | |
| Sharma et al. | A Review: Developments In Commercial Explosives Over The Years | |
| RU2233426C2 (en) | Method for destruction by group action of ammunitions | |
| Homburg | R. Meyer J. Köhler |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| MK1 | Application lapsed section 142(2)(a) - no request for examination in relevant period |