WO2007053143A1 - Explosive formulation - Google Patents
Explosive formulation Download PDFInfo
- Publication number
- WO2007053143A1 WO2007053143A1 PCT/US2005/039617 US2005039617W WO2007053143A1 WO 2007053143 A1 WO2007053143 A1 WO 2007053143A1 US 2005039617 W US2005039617 W US 2005039617W WO 2007053143 A1 WO2007053143 A1 WO 2007053143A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- component
- formulation
- fuel material
- solid fuel
- explosive
- 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.)
- Ceased
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C06—EXPLOSIVES; MATCHES
- C06B—EXPLOSIVES OR THERMIC COMPOSITIONS; MANUFACTURE THEREOF; USE OF SINGLE SUBSTANCES AS EXPLOSIVES
- C06B31/00—Compositions containing an inorganic nitrogen-oxygen salt
- C06B31/28—Compositions containing an inorganic nitrogen-oxygen salt the salt being ammonium nitrate
- C06B31/285—Compositions containing an inorganic nitrogen-oxygen salt the salt being ammonium nitrate with fuel oil, e.g. ANFO-compositions
-
- C—CHEMISTRY; METALLURGY
- C06—EXPLOSIVES; MATCHES
- C06B—EXPLOSIVES OR THERMIC COMPOSITIONS; MANUFACTURE THEREOF; USE OF SINGLE SUBSTANCES AS EXPLOSIVES
- C06B31/00—Compositions containing an inorganic nitrogen-oxygen salt
- C06B31/28—Compositions containing an inorganic nitrogen-oxygen salt the salt being ammonium nitrate
- C06B31/30—Compositions containing an inorganic nitrogen-oxygen salt the salt being ammonium nitrate with vegetable matter; with resin; with rubber
Definitions
- the present invention relates generally to the field of explosive compositions, and methods of making and using same. More particularly, the present invention is a multi- component explosive formulation which finds versatile use in blasting operations such as, but not limited to, mining operations and the like. Even more particularly, though not exclusively, the present invention relates to the manufacture and use of modified forms of Ammonium Nitrate Fuel Oil (ANFO) explosives which have been modified with the incorporation of a solid fuel material.
- ANFO Ammonium Nitrate Fuel Oil
- ANFO is an appropriate mixture of ammonium nitrate and fuel oil. While ANFO remains a popular explosive in the industry, it has inefficiencies, and is relatively expensive due to continually rising costs of its components.
- the present invention provides a multi-component explosive formulation that is ANFO explosives which has been modified with the incorporation of a solid fuel material.
- the present formulation is characterized by lower velocity of detonation, provides results as good as or better than conventional explosives and is less expensive than presently available explosive compositions.
- the present invention comprises an admixture of ammonium nitrate and less than 4% by weight (decreased from the conventional 6% by weight) of fuei oil.
- the carbon molecules in the fuel oil that are chemically necessary for an optimum blast are replaced in the current formulation with a solid fuel material characterized as (1) having a concentration of iiptinite that is higher than normal coals, and (2) having a concentration of pseudovitrinite that is significantly lower than normal coals.
- an explosive formulation is disclosed.
- the present invention relates generally to a multi- component explosive formulation which finds versatile use in blasting operations such as, but not limited to, mining operations and the like. However, as will be understood, the formulation can be applied to other blasting operations. Specifically, it will be noted that the present invention relates to the application of modified forms of Ammonium Nitrate Fuel Oil (ANFO) explosives which have been modified by the. incorporation of a solid fuel material.
- ANFO Ammonium Nitrate Fuel Oil
- the explosive composition of the present invention consists of components configured and correlated with respect to each other so as to attain the desired objective.
- the present invention provides an explosive formulation consisting of at least three components: a dry granular solid component which is an oxidizer, a liquid high-boiling point fuel oil or diesel or the like, and a solid fuel material.
- Each component of the composition of the invention is individually not an explosive. As such, each component can be handled, shipped and stored as either oxidizers or flammable materials. Such classifications are more easily and less expensively shipped than explosives. However, as will be understood, these components, when mixed, form an explosive formulation which finds versatile use in blasting operations such as, but not limited to, mining operations and the like.
- the first component of the composition of this invention is a dry component, which is an oxidizing compound.
- the preferred oxidizer is ammonium nitrate that is manufactured and delivered as a coated spheroid or prill that is in a typical diameter of about .09 inches.
- the first component can be readily selected from among oxidizers conventionally used in the manufacture of explosive compositions to achieve desired properties.
- the second component of the composition is a high-boiling point liquid component.
- the second component is a liquid fuel.
- Conventional ANFO generally comprises a mixture of ammonium nitrate and 6% by weight of fuel oil.
- the current formulation comprises an admixture of the first dry component and less than 4% by weight of the liquid second component.
- the carbon molecules contained in the fuel oil that are chemically necessary for an optimum blast are replaced in the current formulation with the composition's third component a solid fuel material.
- all weights and percent by weight are based on total weight of the formulation.
- the second component can be readily selected from among high-boiling point liquid components conventionally used in the manufacture of explosive compositions to achieve desired properties.
- the third component of the composition is a solid fuel material.
- the third component's main maceraf component (approximately 75%) is vitrinite and also included are the liptinite macerals sporinite, cutinite and resinite.
- the inert macerals fusinite and semifusinite are also present in the third component.
- maceral means those organic units that compose coal mass. As such, coal is composed of macerals which each have a distinct set of physical and chemical properties that control the behavior of coal.
- the third component is further characterized as follows: (1 j the amount of liptinite macerais, particularly cutinite, are higher than normal, and (2) almost no pseudovitrinite (structured coalified wood) is present in the third component.
- the normal amount of liptinite macerais in coal is between 5 - 15% by weight of the coal.
- the amount of liptinite macerais in the third component is approximately 20%.
- the vitrinite group generally includes two sub-groups namely matrix vitrinite, also known as desmovitrinite, and pseudovitrinite, also known as telovitrinite.
- the normal amount of vitrinite macerais in coal is similar to the amount of vitrinite macerais in the third component, approximately 75% by weight. However, of the total 75% by weight of vitrinite macerais found in coal, the normal amount of sub-group pseudovitrinite present is between 25-35%. In contrast, of the total 75% by weight of vitrinite macerais in the third component, there is little trace, near zero, amount of pseudovifrinite present.
- the inherent chemical and physical properties of the third component, as described and used with the first and second components, allows for blasting velocities that match or closely match the natural resonant frequencies of those materials being blasted thereby utilizing only the energy required to fragment and move the rock, and do so in a safer more efficient manner.
- These components of the present formulation may be packaged in separate containers conventionally employed for the desired purpose. Mixing of the components can be accomplished using mixing means known in the art, and does not require mechanical agitation. As such, a motor-driven mixer is not required. Therefore, mixing these dry and liquid components to produce the explosive formulation can be accomplished just prior to the need for the explosive composition.
- the present invention comprises on admixture of the first component (the dry component) and less than 4% by weight of the liquid second component.
- the approximate 4% by weight in the present formulation represents a significant decrease in volume of the liquid component used when compared with the conventional 6% by weight use of prior art explosives.
- the carbon molecules in the second component chemically necessary for an optimum blast are replaced in the current formulation with the third component.
- Application of a lesser volume of the liquid second component as described reduces the cost of the present explosive formulation compared with presently available explosive compositions.
- inclusion of the third component as discussed depletes the required volume of the first component which further reduces the cost of the present explosive formulation compared with presently available explosive compositions.
- the blend ratio of the third component to ANFO is a calculation based on the estimated natural resonant frequency of the rock, shale or other materia! to be blasted.
- the third component can be blended in ranges of about 5% to 50% of the total weight of the formulation.
- the formulation is loaded and delayed, and the shot is initiated as the conventional ANFO method is known in the art. Examples of the invention will now be given.
- ANFO-4 ammonium nitrate mixed with four percent fuel oil by weight
- raw third component material was used because the third component material provides additional fuel to the blasting agent mixture.
- the third component material samples were minus 3/8 inch In size.
- the blends for each test were made using a powder truck equipped with two separate product bins and augers. The auger speed under each bin could bevaried to achieve the appropriate blend.
- the ANFO-4 was placed in one bin and the third component material was placed in the second bin. Material from each bin was augered to a series of common collection augers that mix the blasting agents as they were transferred to the blast hole.
- All of the blast holes drilled for the testing were 9 7/8 inches in diameter. On average the holes were 99 feet deep with 7 feet of backfill, 17 feet of stemming, and a 75 feet powder column.
- the ANFO-4 and washed third component material test holes were positioned in the first row along the highwall face so that if a misfire occurred there would be a minimal amount of material to re- shoot and move with a conventional shot.
- the raw third component material test holes were incorporated into a production shot and were placed in the first and second rows of the shot.
- the highwall face burdens ranged from 22 to 24 feet and all of the holes were spaced 24 feet apart. Each blast hole was initiated with a non-electric detonator and 16 ounce cast primer.
- the surface delay between holes ranged from 25 to 50 milliseconds with each blast having a 500 millisecond down-hole delay.
- The. configuration of all the blast holes in the test is typical of the designs used in normal production shots. Testing began with a 4-hole shot of 100% ANFO-4, followed by three 4-hole shots with blends of 9.1% washed third component material and 90.9% ANFO-4, 21.1% washed third component material and 79.9% ANFO-4, and 29.8% washed third component material and 70.2% ANFO-4.
- ANFO-4 The 100% ANFO-4 shot well and had an average velocity of detonation (VOD) of 12,584 fps. It was slightly underfueled and orange smoke was present at the end of the shot which is typical of that condition. The fragmentation and movement of shot rock was similar to production blasts using ANFO with 6% fuel. The ANFO-4 test was conducted to establish a bench mark velocity for subsequent shots.
- VOD velocity of detonation
- Washed Third Component Material Blends All of the washed blends tested shot well and had constant detonation velocities. There were no misfires. There was some white smoke or steam present and excess fuel continued to burn for an instant after the 51% blend was detonated. In all of the tests, the fragmentation and movement of shot rock was similar to production blasts using ANFO with 6% fuel oil although it appeared that there was a slight decrease in fragmentation and movement as the percentage of third component material exceeded 40%. As the percentage of third component material in the blend increased, the detonation velocity decreased. This relationship is almost linear. In general terms, a 1% increase in third component material decreased the VOD by 82 feet per second. The highest average velocity recorded was 12,601 fps for the 9.1% washed third component material and 78.9 ANFO-4 blend. The lowest was 9,176 fps for the 51% washed third component material and 49% ANFO-4 test.
- Raw Third Component Material Blends All of the raw third component material blends tested shot well and had constant detonation velocity. There were no misfires nor were there signs of incomplete combustion. The fragmentation and movement of shot rock were similar to the washed third component material results. As the percentage of raw third component material was increased, the detonation velocity decreased. On average, a 1% increase in third component material decreased the VOD by 122 feet per second which was higher than the washed third component material blends. The highest average velocity recorded was 13,318 fps for the 14.9% raw third component material and 85.1% ANFO-4 blend. The lowest was 8,361 fps for the 55.7% raw third component material and 44.3% ANFO-4 test.
Landscapes
- Chemical & Material Sciences (AREA)
- Inorganic Chemistry (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Solid Fuels And Fuel-Associated Substances (AREA)
Abstract
Description
Claims
Priority Applications (7)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CNA2005800520024A CN101309885A (en) | 2005-11-02 | 2005-11-02 | explosive preparation |
| PCT/US2005/039617 WO2007053143A1 (en) | 2005-11-02 | 2005-11-02 | Explosive formulation |
| JP2008538852A JP2009514766A (en) | 2005-11-02 | 2005-11-02 | Explosive formulation |
| MX2008005595A MX2008005595A (en) | 2005-11-02 | 2005-11-02 | Explosive formulation. |
| EP05858286A EP1951642A1 (en) | 2005-11-02 | 2005-11-02 | Explosive formulation |
| AU2005337855A AU2005337855A1 (en) | 2005-11-02 | 2005-11-02 | Explosive formulation |
| CA002628195A CA2628195A1 (en) | 2005-11-02 | 2005-11-02 | Explosive formulation |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| PCT/US2005/039617 WO2007053143A1 (en) | 2005-11-02 | 2005-11-02 | Explosive formulation |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| WO2007053143A1 true WO2007053143A1 (en) | 2007-05-10 |
Family
ID=38006170
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| PCT/US2005/039617 Ceased WO2007053143A1 (en) | 2005-11-02 | 2005-11-02 | Explosive formulation |
Country Status (7)
| Country | Link |
|---|---|
| EP (1) | EP1951642A1 (en) |
| JP (1) | JP2009514766A (en) |
| CN (1) | CN101309885A (en) |
| AU (1) | AU2005337855A1 (en) |
| CA (1) | CA2628195A1 (en) |
| MX (1) | MX2008005595A (en) |
| WO (1) | WO2007053143A1 (en) |
Citations (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5505800A (en) * | 1991-02-11 | 1996-04-09 | Technological Resources Pty Ltd. | Explosives |
Family Cites Families (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS5879895A (en) * | 1981-11-02 | 1983-05-13 | 三菱化学株式会社 | Explosive based on ammonium nitrate-carbon mixture |
| JP2003146787A (en) * | 2001-11-08 | 2003-05-21 | Asahi Kasei Corp | Ammonium nitrate explosive composition and method for producing the same |
-
2005
- 2005-11-02 MX MX2008005595A patent/MX2008005595A/en unknown
- 2005-11-02 CN CNA2005800520024A patent/CN101309885A/en active Pending
- 2005-11-02 CA CA002628195A patent/CA2628195A1/en not_active Abandoned
- 2005-11-02 WO PCT/US2005/039617 patent/WO2007053143A1/en not_active Ceased
- 2005-11-02 AU AU2005337855A patent/AU2005337855A1/en not_active Abandoned
- 2005-11-02 JP JP2008538852A patent/JP2009514766A/en active Pending
- 2005-11-02 EP EP05858286A patent/EP1951642A1/en not_active Withdrawn
Patent Citations (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5505800A (en) * | 1991-02-11 | 1996-04-09 | Technological Resources Pty Ltd. | Explosives |
Also Published As
| Publication number | Publication date |
|---|---|
| JP2009514766A (en) | 2009-04-09 |
| CN101309885A (en) | 2008-11-19 |
| MX2008005595A (en) | 2008-09-03 |
| EP1951642A1 (en) | 2008-08-06 |
| CA2628195A1 (en) | 2007-05-10 |
| AU2005337855A1 (en) | 2007-05-10 |
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