Patent Application
20160146587
The present invention relates to the manufacture of explosive compositions, in particular emulsion explosive compositions that are tailored to provide desired blasting properties. The present invention also relates to the integration of such manufacture in a blasting operation in which the explosive composition that is manufactured is provided in a blasthole.
Detonation energy of commercial explosives can be broadly divided into two forms—shock energy and heave energy. Shock energy fractures and fragments rock. Heave energy moves blasted rock after fracture and fragmentation. In general the higher the velocity of detonation (VOD) of an explosive the higher proportion of shock energy the explosive is likely to exhibit.
Certain mining applications require the use of explosives that exhibit a combination of low shock energy and high heave energy. This allows fragmentation to be controlled (high shock energy produces significant amounts of dust sized fines) and in turn reduces excavation costs. In softer rock and coal mining applications, for example, the use of explosives that provide a relatively high proportion of heave energy can lead to significant savings downstream for the mine operation because collection of blasted rock then becomes easier. In quarry applications, fragmentation control and reduction of fines is also very attractive.
Current commercial explosives offer a range of shock and heave energies. For example, ANFO (ammonium nitrate/fuel oil) tends to provide a particular balance between shock and heave energies (low shock energy and high heave energy), and is frequently used as a reference point for assessing blast performance. In fact, ANFO with all of its ammonium nitrate present as prill exhibits what is conventionally believed to be an excellent combination of shock (fragmentation) and heave properties for many rock blasting and collection situations.
In contrast, homogeneous fluid explosive compositions, such as ammonium nitrate emulsion explosives tend to provide high shock energy and low heave energy. It is well known that such emulsion explosives tend to have relatively high velocities of detonation and correspondingly high pressure in the chemical reaction zone. This results in a high shock explosive that is well suited to fragmenting rock, but that has relatively low heave energy to move fragmented rock. Various water gel explosives provide a similar range of performance to emulsion explosives.
In practice, materials that modify explosive characteristics, such as ammonium nitrate (AN) prill are conventionally added to emulsion explosives to enhance their overall heave properties. Prills are understood to contribute to a late burn in the post detonation zone and this manifests itself as heave energy rather than shock energy.
The explosive properties of prill-containing explosive compositions are closely related to the explosive characteristics of the prill itself and, in turn, the explosive characteristics are influenced by factors including the physical features, internal structures and chemical composition of the prill. However, such factors may vary within a wide range depending on such things as the manufacturing technology used to produce the prill, the type and/or content of additives (and/or contaminants) present in the prill, the manner in which the prill is stored and/or transported, and the context of use of the explosive, including the degree of confinement and environmental factors, such as temperature and humidity. As a result, the detonation performance (including the energy release characteristics) of conventional prill-containing explosives tends to be highly variable. Explosive formulations with a high concentration of prill are also very difficult to pump into a blasthole. In contrast, emulsion explosives and slurry formulations are readily pumped and particularly useful in wet conditions. ANFO based formulations can only be used in wet conditions after dewatering of the boreholes.
A further consideration in relation to the use of ANFO and AN prill-containing emulsion explosives is the cost of manufacture of AN prill. AN prill manufacturing towers represent a significant fraction of capital expenditure associated with an ammonium nitrate production facility. Prilling is also a highly energy intensive process that adds significantly to the carbon footprint associated with these type of explosives.
Against this background, the Applicant has devised an explosive for commercial blasting operations that does not require the use of ammonium nitrate prill and that therefore does not suffer the potential problems associated with the use of prill, but that can achieve at least comparable rock blasting performance as currently used ANFO and AN prill-containing explosives. The explosive composition devised by the Applicant exhibits the desirable features of conventional ANFO and AN prill-containing explosives in terms of detonation energy ratio as between shock and heave energies, but that is free of the practical (and economic) constraints associated with the use of such prill-containing conventional explosives.
More specifically, the Applicant has devised an explosive composition comprising a liquid energetic material and sensitizing voids, wherein the sensitizing voids are present in the liquid energetic material with a non-random distribution, and wherein the liquid energetic material comprises (a) regions in which the sensitizing voids are sufficiently concentrated to render those regions detonable and (b) regions in which the sensitizing voids are not so concentrated. The explosive composition is therefore defined with reference to its internal structure. Explosive compositions that have this particular internal structure/void distribution exhibit desirable features of conventional ANFO and AN prill-containing explosives in terms of detonation energy ratio as between shock and heave energies, but that is free of the practical (and economic) constraints associated with the use of such prill-containing conventional explosives. For ease of reference the explosive compositions that may be produced in accordance with the present invention are referred to in general terms as having a non-random distribution of sensitizing voids in a liquid energetic material. Such explosive compositions are described in the Applicant's International patent application nos. PCT/AU2012/001527 and PCT/AU2012/001528, the contents of which are incorporated herein by reference. The invention may have particular applicability to such explosive compositions. The contents of Applicant's International patent application nos. PCT/AU2012/001527 and PCT/AU2012/001528 are set out in detail.
Moreover, with explosive compositions that have a non-random void distribution, blast performance/characteristics can be adjusted in order to suit an array of different blasting requirements. For example, it may be desired to vary explosive performance across a blast field by loading individual blastholes with an explosive formulation that is most well suited to the characteristics of each blasthole, the prevailing geological conditions and/or the intended blast outcome. Conventional blasting practice has generally been to deliver the same explosive formulation to each blasthole in a blast field irrespective of blasthole characteristics. This approach can yield acceptable results but there is scope for improvement by designing or matching the explosive formulation used on a hole-by-hole basis. However, this brings with it certain practical challenges, not least how to undertake formulation manufacture, formulation variation and blasthole loading in a manner that is convenient and economical to implement. The present invention seeks to provide solutions that meet these practical challenges.
Accordingly, in one embodiment, the present invention provides a mobile manufacturing and delivery platform (MMDP) that is adapted to provide in a blasthole an explosive composition comprising a liquid energetic material and sensitizing voids, the sensitizing voids being present in the liquid energetic material with a non-random distribution. In an embodiment of the invention the manufacturing methodology employed in the MMDP is suitably flexible so that the characteristics of the explosive composition (e.g. the distribution and/or the concentration of voids), and thus the blasting performance, can be varied with ease so that tailored blasting solutions can be provided between different blastholes in a blastfield.
In an embodiment the present invention also provides a portable module (PM) that is adapted to provide in a blasthole an explosive composition comprising a liquid energetic material and sensitizing voids, the sensitizing voids being present in the liquid energetic material with a non-random distribution. The PM will include the necessary componentry to undertake manufacturing and delivery of explosive compositions as required in the context of the invention.
The componentry required in the MMDP and PM and the working inter-relationship of componentry will become apparent as the invention is explained in greater detail. As will be evident, preferably the MMDP/PM allows manufacture and loading into blastholes of explosive compositions without the use of augers or other heavy solid explosives handling equipment. This enables process functionality, loading capacity and safety to be enhanced. The intention is to provide a seamless on-site manufacturing and blasthole loading system that is integrated in mobile form.
The present invention also provides a method of providing in a blasthole an explosive composition comprising a liquid energetic material and sensitizing voids, the sensitizing voids being present in the liquid energetic material with a non-random distribution, which method comprises manufacturing and delivering the explosive composition using a MMDP (or PM) in accordance with the present invention.
In another embodiment the present invention provides a method of (commercial) blasting in which an explosive composition is manufactured and delivered into a blasthole using a MMDP (or PM) in accordance with the present invention, and the explosive composition subsequently initiated/detonated. The explosive composition is used in exactly the same manner as conventional explosive compositions. The explosive compositions are intended to be detonated using conventional initiating systems, for example using a detonator and a booster and/or primer.
In another embodiment the present invention may be applied to achieve specific (designed) bulk detonation energy output in an explosives material by determining a distribution function (DF) template that is representative of that energy output and then formulating an explosive composition consistent with that DF template. This formulation is undertaken in accordance with the present invention by suitable placement and distribution of sensitizing voids within a liquid energetic material. DF templates and related aspects are disclosed in the Applicant's International patent application no. PCT/AU2012/001528.
Notably, the internal structure of the explosive composition is such that the two energetic materials are present as discrete regions. These regions may be distributed uniformly or randomly throughout the composition. The volume proportion, size and spatial arrangement of the regions define the bulk explosive structure. It has been found that the nature of the energetic liquids used and the bulk structure of the resultant explosive composition influence the energy release characteristics of the explosive composition. Thus, the voids, after their reaction determine the amount of shock energy and the regions of void-free liquid energetic material determine the heave energy. Quantitatively, the amount of shock energy is a function of the “total voidage volume” and the amount of heave energy is a function of the void-free component volume fraction.
Importantly, this allows the energy release characteristics of an explosive composition to be understood and controlled by varying the combination of energetic liquids used and/or the arrangement of the energetic liquids within the bulk of the explosive composition. In turn this enables the detonation properties of the explosive composition to be tailored to particular rock/ground types and to particular mining applications. As will become clear, the formulations that may be produced in accordance with the present invention may be varied by components selection and/or by manipulating process parameters, such as flow rates of components, and/or by varying hardware componentry that is used. The invention may thus be readily applied to vary explosive formulation design, even between individual blastholes.
Broadly speaking, the design aspect of the present invention is likely to involve the following sequence of steps.
Throughout this specification and the claims which follow, unless the context requires otherwise, the word “comprise”, and variations such as “comprises” and “comprising”, will be understood to imply the inclusion of a stated integer or step or group of integers or steps but not the exclusion of any other integer or step or group of integers or steps.
The reference in this specification to any prior publication (or information derived from it), or to any matter which is known, is not, and should not be taken as an acknowledgment or admission or any form of suggestion that that prior publication (or information derived from it) or known matter forms part of the common general knowledge in the field of endeavour to which this specification relates.
Also included are FIGS. 1-8 from PCT/AU2012/001527 and FIGS. 1-19 from PCT/AU2012/001528, and these are clearly identified as such.
The present invention seeks to provide tailored blasting solutions by use of equipment (MMDP or PM) that has the capability to manufacture and deliver to a blasthole an explosive composition having a non-random distribution of sensitizing voids distributed in a liquid energetic material. The explosive characteristics of such explosive compositions are directly related to the distribution of sensitizing voids present and the invention provides methodologies by which this internal structure may be adjusted in a batch-wise fashion so that the characteristics and thus the blasting performance of explosive composition may be varied between blastholes, as required. This would be done in a pre-determined manner in accordance with an overall blast design. In allowing such variation to be achieved in a practical and economic manner, the present invention may provide a further parameter that can be used to optimize the performance of a blast.
In the context of the present invention, the term “explosive composition” means a composition that is detonable per se by conventional initiation means at the charge diameter being employed.
Herein the term “liquid energetic material” is intended to mean a liquid explosive that has stored chemical energy that can be released when the material is detonated. Typically, a liquid energetic material would require some form of sensitization to render it per se detonable. Thus, the term excludes materials that are inherently benign and that are non-detonable even if sensitized, such as water. The energetic materials used in the invention are in liquid form, and here specific mention may be made of explosive emulsions and water gels. Such emulsions and water gels are well known in the art in terms of components used and formulation. The invention is believed to have particular applicability in the context of producing emulsion explosive compositions by sensitizing emulsion compositions.
The explosive compositions manufactured in accordance with the present invention have a characteristic structure with respect to the distribution of sensitizing voids in a liquid energetic material. One skilled in the art will readily understand what is meant by sensitizing voids in this context. The sensitizing voids may be glass micro-balloons, plastic micro-balloons, expanded polystyrene beads, or any other conventionally used (solid) sensitizing agent. However, it is possible to implement the present invention using gas as the sensitizing agent. For example, this may achieved using a chemical gassing solution that reacts with one or more components of a liquid energetic material to generate gas bubbles, and it is these gas bubbles that have a sensitizing effect. It will be appreciated that when such chemical gassing solutions are used in the method of the present invention, sensitizing voids per se are not being delivered into the liquid energetic material. Rather, droplets of chemical gassing solution would be delivered into the liquid energetic material with chemical gassing of the liquid energetic material taking place subsequently since the gas-generating reaction is not instantaneous but rather slow. The effect is still the same in terms of achieving the desired arrangement of voids in the explosive composition that is produced but the mechanism of void production is obviously different.
Herein unless explicitly stated or context clearly dictates otherwise, the term sensitizing voids is intended to embrace the use of solid and/or gaseous sensitizing agents as are commonly used in the art. Likewise, unless explicitly stated or context clearly dictates otherwise, reference to the delivery of sensitizing voids into a liquid energetic material is intended to embrace the delivery of sensitizing agents per se and also the delivery of chemical gassing solution that will give rise to gas bubbles that provide a sensitizing effect. Generally, when a chemical gassing solution is used the present invention should be implemented so that the gassing reaction yields gas bubbles after blasthole loading. Attempts to pump a pre-gassed liquid energetic material are likely to result in loss of gas bubbles and/or coalescence of gas bubbles, and these effects are undesirable with respect to sensitization.
The MMDP described above is mobile in the sense that it may readily be moved between blastholes in a blast field. The MMDP usually takes the form of a vehicle (truck) that is equipped with the necessary componentry to undertake manufacturing and delivery of explosive compositions as required in the context of the invention.
The MMDP may comprise: a source for supplying the liquid energetic material; at least two delivery lines for conveying respective streams of the liquid energetic material; a void delivery system for producing sensitizing voids in at least one of the streams of liquid energetic material; a mixer for mixing the streams of liquid energetic material to produce the explosive composition; and a blasthole loading hose. In this embodiment the explosive composition is formed before being delivered into the blasthole.
The PM may comprise: at least two delivery lines for conveying respective streams of the liquid energetic material from a source for supplying the liquid energetic material; a void delivery system for producing sensitizing voids in at least one of the streams of liquid energetic material; a mixer for mixing the streams of liquid energetic material to produce the explosive composition; and a loading hose for delivery of the explosive composition into a blasthole. In this embodiment the explosive composition is formed before being delivered into the blasthole.
Related to these embodiments the MMDP or PM may further comprising a device for bringing respective streams of liquid energetic material together prior to entry to the mixer, the device being adapted to minimize mixing of the streams before they enter the mixer.
In another embodiment the MMDP may comprise a source for supplying the liquid energetic material; at least two delivery lines for conveying respective streams of liquid energetic material from the source; a void delivery system for producing sensitizing voids in at least one of the streams of liquid energetic material; a blasthole loading hose for the simultaneous delivery of the streams of liquid energetic material into a blasthole; and a mixer provided at the end of the loading hose for mixing the streams of liquid energetic material to produce the explosive composition.
In a related embodiment the PM may comprise: at least two delivery lines for conveying respective streams of a liquid energetic material from a source for supplying the liquid energetic material; a void delivery system for producing sensitizing voids in at least one of the streams of liquid energetic material; a loading hose for the simultaneous delivery of the streams of liquid energetic material into a blasthole; and a mixer provided at the end of the loading hose for mixing the streams of liquid energetic material to produce the explosive composition.
In these embodiments it will be understood that the individual components (i.e. the streams of liquid energetic material) used for forming the explosive composition are delivered into the blasthole with mixing of the components to form the explosive composition taking place in the blasthole. The streams of liquid energetic material may be delivered into the blasthole for mixing using a single loading hose with a mixer provided at its end. In this case the MMDP or PM may comprise a device for bringing respective streams of liquid energetic material together prior to entry to the loading hose, the device being adapted to minimize mixing of the streams before they enter the loading hose. The device may comprise inlets for respective streams of the liquid energetic material, one or more baffles to minimize mixing of the streams and a single outlet. The baffles may combine the respective streams as discrete layers to provide a single stream at the outlet. In an alternative the baffles combine the respective streams in an annular arrangement to provide a single stream at the outlet.
In an alternative embodiment each stream of liquid energetic material may be delivered into the blasthole through respective loading hoses with each loading hose feeding a stream into a mixer for forming the explosive composition. This approach may be advantageous as it will ensure that there is no mixing of the streams in the loading hose before entry into the mixer.
The source for supplying the liquid energetic material may be a storage tank containing the liquid energetic material. However, in an embodiment, the liquid energetic material may be supplied directly as it is being produced. In this case the source would be a facility, system or device that produces the liquid energetic material. Thus, the MMDP or PM may also be equipped with chemicals and componentry to produce the liquid energetic material as it is required.
When the liquid energetic material is supplied from a storage tank the individual streams of liquid energetic material may be provided in a number of ways. In one embodiment individual delivery lines, i.e. at least two delivery lines, may extend directly from the storage tank. In this case each delivery line will have its own associated pump in order to convey the respective streams. In this embodiment the storage tank may comprise a number of independent compartments and one or more valves for controlling which compartment feeds the respective delivery lines. For example, the storage tank may comprise at least two independent compartments and a valve for controlling which compartment feeds each of the delivery lines. Thus, a single storage tank may be equipped to provide multiple types of liquid energetic material each having different characteristics. This provides increased flexibility in terms of the range of explosive compositions that can be produced with the valve(s) regulating which liquid energetic material is being supplied to each delivery line.
In another embodiment the individual streams of liquid energetic material may be derived from a single delivery line that extends directly from the storage tank. In this case a flow divider may be used for dividing the stream of liquid energetic material into respective individual streams of liquid energetic material. In this case the same pump may be used for conveying the liquid energetic material and for delivery of liquid energetic materials or explosive composition into the blasthole.
Related to this embodiment the storage tank may comprise a number of independent compartments and a valve for controlling which compartment feeds the delivery line running off the storage tank. For example, the storage tank may comprise at least two independent compartments and a valve for controlling which compartment feeds the delivery line. Thus, a single storage tank may be equipped to provide multiple types of liquid energetic material each having different characteristics. This provides increased flexibility in terms of the range of explosive compositions that can be produced with the valve(s) regulating which liquid energetic material is being supplied to the delivery line.
In an embodiment the MMDP has a high volume storage tank (for example 10,000 to 35,000 litres) for liquid energetic material. The MMDP may be constructed by suitable modification of a vehicle equipped with a large volume storage tank and associated pump componentry for delivery from the tank. This modification will involve fitting to the vehicle the various componentry required to implement the methodology of the invention so that manufacture and delivery into a blasthole of explosive composition can be undertaken using liquid energetic material from the storage tank. It may be preferred that the storage tank is of high volume, such as 10,000 to 35,000 litres.
In an embodiment of the invention, the PM is adapted to be retro-fitted to an existing mobile manufacturing unit (MMU). This embodiment allows existing MMUs to be modified in order to undertake manufacturing and loading of explosive compositions in accordance with the present invention.
In another embodiment, the PM is provided in a container, on a trailer or on a skid, pallet, flat tray or the like. In this case the PM is not self-propelling and it must be moved from location to location. The PM may be adapted to co-operate with an existing (conventional) MMU and here it may be convenient for the PM to be provided on a trailer that can be pulled by such an MMU.
In another variant, the PM may be provided for use in applications where vehicle access is not readily possible, such as in underground or tunneling applications. In this case the PM may be conveniently provided in a container or on a skid, pallet, flat tray or the like, that can be lifted and taken to the site of intended use, for example using a forklift.
The MMDP and PM will invariably also include a control system to regulate the function of hardware components and their interaction.
A motor will be used to drive pumps and ancillary componentry of the MMDP/PM. The motor may be hydraulic, pneumatic or electric, preferably hydraulic.
The liquid energetic material is typically sourced and supplied from a centralised, dedicated facility and transported to the site of its actual use, where it may be stored under suitably controlled conditions in large bulk hoppers. This is consistent with the typical approach for supply of a liquid energetic material for manufacture of a conventional bulk emulsion explosive. In accordance with the invention, liquid energetic material is transferred from the bulk hopper to a storage hopper provided on the mobile MMDP (or conventional MMU equipped with PM). This may be done using an onboard gear pump or the like, or a bulk hopper service pump.
In an embodiment of the invention the internal structure required in the explosive composition is achieved by suitable blending of individual streams that have different void concentrations. Typically, this would involve combining together a first liquid energetic material and a second liquid energetic material to provide regions of the first liquid energetic materials and regions of the second liquid energetic material, wherein the first liquid energetic material is sensitized with sufficient sensitizing voids to render it detonable and wherein the second energetic liquid has different detonation characteristics from the sensitized first liquid energetic material. In this embodiment, usually the first liquid energetic material is void sensitized and the second liquid energetic material is not void sensitized or void sensitized but to a lower extent than the first liquid energetic material. In the following, for simplicity, reference will be made to blending together of a void sensitized stream of liquid energetic material with a liquid energetic material that is not void sensitized. However, it will be appreciated that this is not essential and that the invention may be implemented by blending together of a void sensitized liquid energetic material with another liquid energetic material that is void sensitized but to a lower extent. In this case the intention is to produce an explosive composition having a non-random distribution of differentially sensitized regions.
Typically, the liquid energetic material is supplied from a storage container or hopper and pumped though a line (tube/pipe) using a suitable pump. The flow rate of the liquid energetic material is generally in the range of 50 to 1000 kg/min, more preferably 50-450 kg/min. The exact flow rate will depend upon application and the specifics of the methodology being applied in accordance with the invention.
The individual streams may be derived from a common source (e.g. a single hopper or tank) of liquid energetic material. Independent streams of liquid energetic material are generated from the source with one stream being void sensitized and the other not, followed by blending of the streams to provide an explosive composition having the desired internal void structure. Usually, for simplicity, this embodiment is carried out by generating two independent streams. However, this is not essential and more than two streams may be generated and subsequently combined to produce an explosive composition with requisite internal structure.
In an embodiment the hopper or tank may include independent compartments for storage and supply of different types of formulation of liquid energetic material, thereby increasing flexibility in the range of explosive compositions that may be produced. The compartments may be provided by internal partitioning of the hopper or tank, each compartment having a delivery hose running off it and valves to control flow of liquid energetic material.
It is possible for the independent streams to be derived from independent sources of liquid energetic materials having different characteristics and this may give increased flexibility in terms of formulation design. Equally, the invention may be implemented with multiple sources of liquid energetic material with the capability of generating independent streams from either source or from each source of liquid energetic material. In such cases, valves will be used to select the source(s) of liquid energetic material from which the independent streams are generated.
In the following discussion reference will be made to using a single source of liquid energetic material, but unless context dictates, this should not be regarded as limiting. Likewise, in the following various aspects of design and componentry combination will be discussed and again this should not be regarded as limiting, unless context dictates otherwise. One skilled in the art will appreciate that certain design features that are discussed may readily be combined with other design features to produce a suitably operative system.
The (single) source of liquid energetic material may have one or two outlets (i.e. conduits) for conveying liquid energetic material for manufacture and blasthole loading of explosive composition. When the source includes a single outlet line, a single pump may be used to generate a flow of liquid energetic material with a downstream device splitting the flow into two independent streams that flow in parallel with each other. One of the parallel streams is processed to introduce sensitizing voids. The resultant void sensitized stream is suitably combined with the parallel flowing stream of non-sensitized liquid energetic material to produce an explosive composition having the desired internal structure. This arrangement has the advantage of requiring a single pump to generate the two flow streams of liquid energetic material making the process easier and thus safer to monitor and control flow. The use of a single pump may also reduce capital costs and enable the system to be retrofitted to existing mobile manufacturing units (MMUs) at low cost.
In the case of a single outlet line and single pump, the flow splitting device may include some form of flow control valve(s) to regulate flow of the independent streams produced, or a flow control valve may be included in one or both of the independent outlet lines running off of the flow splitting device. Regulation of the flow of one or both independent flow streams of liquid energetic material will give enhanced process control and flexibility in terms of product design.
In an alternative embodiment, the source of liquid energetic material (i.e. the hopper, bin, etc.) may include two outlet lines for liquid energetic material. In this case each line will require its own pump to generate a flow stream of liquid energetic material. One stream will be processed to introduce sensitizing voids with the resultant void sensitized stream then being suitably combined with the stream of non-sensitized liquid energetic material to produce an explosive composition having the desired internal structure. Whilst requiring multiple pumps, this design allows for easier, more precise control of the relative flow rates of the independent streams, providing more flexibility in the explosive compositions that may be produced.
In the foregoing embodiments, the pumps used are of conventional design and one skilled in the art would be aware of the types and sizes of pumps to be used to achieve required flow rates, as well as how the pumps are operated in the field. The delivery lines used to convey liquid energetic material/void sensitized liquid energetic material may include flowmeters and flow control componentry, but again these would be of conventional design.
In an embodiment of the invention sensitizing voids are delivered into a liquid energetic material and the resultant void sensitized liquid energetic material blended with an unsensitized liquid energetic material to form an explosive composition before delivery of the explosive composition into the blasthole. In this case, it is important that the distribution of voids in the liquid energetic material is retained following blasthole loading. When a chemical gassing solution is added prior to loading in the blasthole, gassing should take place in the blasthole. In this case, it is important that the required distribution of (droplets of) chemical gassing solution in the liquid energetic material is retained following blasthole loading so that gas bubbles will then be generated with the required distribution.
In another embodiment of the invention sensitizing voids are delivered into a liquid energetic material and the resultant void sensitized liquid energetic material then blended with an unsensitized liquid energetic material to form an explosive composition during delivery of these individual components into the blasthole. When a chemical gassing solution is used gassing should take place in the blasthole. In this case, it is important that the required distribution of (droplets of) chemical gassing solution in the liquid energetic material is produced during blasthole loading so that gas bubbles will be then be generated with the required distribution.
As noted above, formation of the explosive composition can involve blending of a void sensitized liquid energetic material (or liquid energetic material containing droplets of chemical gassing solution) with a liquid energetic material that is unsensitized. In embodiments of the present invention an explosive composition having the desired internal structure is formed before delivery into a loading hose that conveys the explosive composition into a blasthole. Thus, it is important that the internal structure of the explosive composition with respect to void distribution is retained during blasthole loading.
This blending may be achieved by use of a mixer that is capable of layering the void sensitized liquid energetic material (or liquid energetic material containing droplets of chemical gassing solution) into a continuum of the unsensitized liquid energetic material. Alternating layers of void (or gasser solution) rich component and unsensitized component may be achieved by repeated division, transposition and recombination of liquid layers. It has been found that suitable mixing may be achieved using an in-line static mixer, such as an SMX mixer or a helical static mixer with multiple elements. The use of one or more additional static mixers arranged in series may reduce the dimensions of void sensitized and unsensitized regions that are produced.
It may be convenient for the mixer to be provided with integrated inlets (delivery lines/ports) for the individual components. For example, the mixer may have a Y-shaped configuration having respective inlets for these components and a single outlet for the resultant blended product.
In a further embodiment, the inlets of the mixer may be configured to deliver a stream comprising a core flow of one liquid energetic material surrounded by an annular flow of the other liquid energetic material. Delivering this type of concentric stream of components to the mixer may assist in the production of a uniform product of mixing.
In a further embodiment of the invention, the MMDP (or PM) is adapted to deliver respective streams of the components to a variety of different mixers that have different sizes and volume outputs. The size of the mixer used to formulate an explosive composition may thus be varied depending upon the size of blasthole loading hose being used. This will also give application flexibility as the same equipment may then be employed to service different blasting contexts that use different borehole sizes. For example, allowing for use of different mixers with various sizes on the same MMDP (or PM) may enable the same equipment to be used in both quarrying and mining applications. In this embodiment, multiple mixers of different sizes are used with flow control valves being used to control flow of respective streams of void sensitized and unsensitized liquid energetic material to the desired mixer. These flow control valves are positioned upstream of the mixers in the component delivery lines to the mixers.
Once produced, the blend having the required internal void distribution is loaded into a blasthole through a loading hose. To minimize shearing, an annular layer/stream of water may be provided around the blend. This approach and suitable water injection systems are known in the art.
In yet another embodiment, mixing of respective streams of the respective components takes place in the blasthole itself. In this case, individual streams of the components may be delivered through respective loading hoses that deliver the individual streams to a mixer provided at the end of the hoses. The mixer is thus provided in the blasthole during loading. Each loading hose may be lubricated with an annular layer/stream of water to enhance delivery of the individual streams of the components to the mixer. The mixer may have the same characteristics as set out above. The loading hoses will typically be lowered and raised into and out of the blasthole using a reel system.
Care should be taken when delivering components or a blend of components into a blasthole so that the desired distribution of components is achieved or maintained. Various factors may influence this including, for example, the rate of pumping and the rate at which the loading hose is withdrawn from the blasthole as loading progresses. Preferably, the hose is initially lowered to the base of the blasthole before starting the pump. Upon starting the pump, the hose may remain stationary until the end of the hose becomes submerged in components/blend being pumped. The hose is then raised in a controlled manner such that the end of the hose remains below the surface of the rising column of component/blend delivered. For this purpose, the hose reel may be powered by a variable speed motor, the speed of which can be matched to the velocity of the rising column.
Various specific embodiments of how the present invention may be implemented are now presented. For the purposes of illustration the liquid energetic material used in these specific embodiments is an emulsion of an oxidiser salt (ammonium nitrate) in oil (referred to as ANE in the related figures). This emulsion is sensitized by delivering into it a chemical gassing solution prior to blasthole loading with gas bubbles being subsequently generated in the emulsion following blasthole loading. It will be appreciated however that variations are possible whilst maintaining the fundamental design features of each specific embodiment. For example, different means of sensitization may be employed. The various embodiments are described in the context of a mobile manufacturing and delivery platform but the fundamental design of each embodiment may have wider applicability.
The specific embodiments described may be capable of being retrofitted to existing MMU designs, thereby allowing conventional ANFO/heavy ANFO and void sensitized explosive compositions to be delivered from the same truck.
This specific embodiment is illustrated within
Into one of the streams of liquid energetic material is delivered a chemical gassing solution before that stream is combined with the other stream of unsensitized liquid energetic material. At least one dedicated (gasser) pump will be used to deliver the chemical gassing solution. Optionally, a second pump may be used to deliver a second component for the gassing system Subsequently, the stream to which gassing solution has been added is combined within the other flow stream (unsensitized liquid energetic material) in a suitable mixing device that will blend the two streams in a manner so as to achieve the desired internal structure.
In the specific embodiment shown, flow control valves are provided that allow the flow streams to be directed, depending upon intended application and loading hose diameter, to different sized mixers. For example, the flow control valves may be arranged to cause the two streams to be mixed in a 1″ or 2″ mixer. This allows greater flexibility of use of the MMDP or the PM. This approach is not restricted to this particular embodiment and the use of an array of different mixers may be applied to other embodiments. Optionally, flowmeters can be installed on the emulsion lines for monitoring purposes. A quick release mechanism may be used to allow the size and/or type of mixer to be interchanged.
After blending/mixing, the blend can be delivered into a blasthole through a loading hose. An annular layer of water may be provided in the loading hose to aid lubrication, reducing unwanted shearing as the product is delivered through the hose. A water delivery line and associated pump and valve componentry is shown in
The height of the explosive column increases as the explosive is loaded into the hole. Preferably, the hose is initially lowered to the base of the borehole before starting the pump. Upon starting the pump, the hose remains stationary until the end of the hose becomes submerged in the explosive. The hose is then raised in a controlled manner such that the end of the hose remains below the surface of the rising column of explosive. For this purpose, the hose reel may be powered by a variable speed motor, the speed of which can be matched to the velocity of the rising explosive column. The aim is to ensure that the product in the blasthole retains the desired structure with respect to the positioning and dimensions of the discrete regions of sensitized and unsensitized liquid energetic material.
This specific embodiment is illustrated in
A flow splitting device downstream of the pump can be used to produce two independent flow streams of liquid energetic material. One of the streams produced by flow splitting is processed by delivering into it a chemical gassing solution. Thereafter this stream is blended with the other stream of unsensitized liquid energetic material, previously produced by flow splitting, to achieve the desired (precursor) structure with respect to distribution of (droplets of) chemical gassing solution. Flowmeters on each of the lines, through which the streams flow, may be connected to a control system that drives one or more proportioning valves to control the flow rate of each stream to the mixer.
As a generally applicable feature, the proportioning valve(s) may contain a position indicator, allowing the system to be pre-calibrated to determine the valve position required to produce the desired ratio of flow rates of the two streams, avoiding the requirement for a flowmeter.
Once formed, the explosive composition may be delivered into a blasthole using a single loading hose that has a water injection system for lubricating the flow. This arrangement is the same as described in relation to specific embodiment 1.
Although not shown, the arrangement in
This specific embodiment is illustrated in
As noted above, the mixer may have a Y-shaped configuration having respective inlets for components and a single outlet. The outlet contains a central baffle to prevent unintended mixing of the two components prior to entering a static mixer or loading hose. According to one option (
In a variant, the streams are combined in a Y-piece prior to flowing down a hose, with blending occurring at the end of the hose. This may reduce unintentional mixing occurring during delivery through the hose. This arrangement is shown in
Specific embodiment 5 is related to specific embodiment 4, and here the Y-piece may be provided as an injector to produce concentric streams of differentially sensitized liquid energetic material, for example gassed and ungassed liquid energetic material. The injector is designed so that one stream flows down a central inner tube to provide a core stream, whilst a second stream of liquid energetic material is injected in an annular fashion, i.e. around the core stream. This generates concentric streams and this may be advantageous when blended using a mixer. There may be reduced risk of unintended mixing in the delivery hose when this injector design is used to feed components to a mixer provided at the end of a loading hose. Moreover, the final structure may be independent of mixer orientation when using a helical mixer.
As noted, the present invention may be applied to produce explosive compositions of the type described in PCT/AU2012/001527 and PCT/AU2012/001528. For reference the content of each of these International patent applications is discussed in more detail below.
In an embodiment of the invention, the MMDP/PM is also adapted to provide, in a blasthole, a conventional void-sensitized explosive composition, that is an explosive composition in which the void distribution is random. This may be done by generating a void-containing stream of liquid energetic material using relevant componentry of the MMDP/PM and by-passing the step of blending/mixing that stream with a stream of unsensitized liquid energetic material. This embodiment provides enhanced flexibility with respect to the type of explosive compositions that may be produced using the MMDP/PM of the invention.
This embodiment may actually give rise to an entirely new approach to manufacturing and delivery. Here it may be noted that a single, conventional MMUs may be adapted to provide multiple different types of product depending upon the blast performance required. Thus conventional MMUs may be adapted to provide a “dry” product such as ANFO that must be loaded into a blasthole using augers or other heavy solid explosives handling equipment and pumpable products such as emulsion explosives and blends of emulsion explosives and prill. The fact that the explosive compositions of the invention can be produced to provide the same type of blasting performance as ANFO and prill-containing emulsions means that the same level flexibility in terms of blasting performance can be achieved using fewer products. For example, in the case that a single MMU is adapted to deliver (a) ANFO, (b) a conventional void sensitized emulsion explosive and (c) a conventional void-sensitized emulsion explosives dosed with prill, using the present invention the same flexibility in terms of blasting performance can be achieved by providing (a) a void-sensitized emulsion explosive in which the void distribution is non-random and (b) a conventional void sensitized emulsion explosives. This may give raise to advantages in terms of enabling process functionality, loading capacity and safety. Furthermore, it allows the use of augers or other heavy solid explosives handling equipment to be avoided.
Embodiments of the invention are now illustrated with reference to the following prophetic examples.
A mobile manufacture and delivery platform (MMDP) is used for manufacture and delivery of an explosive with non-random void distribution in accordance with Specific Embodiment 1. The MMDP includes raw material hoppers for ammonium nitrate emulsion, two pumps for producing two streams of emulsion, flowmeters for measuring the emulsion flow rates, a gasser delivery system for supplying gasser solution to one of the emulsion streams and static mixers for dispersing the gasser. The MMDP also includes three-way valves to direct the emulsion streams to two different sized helical static mixers for blending, and separate outlet hoses from each helical static mixer arrangement for loading blastholes. One of the hoses is contained on a motorized hose reel to lower and retract the hose whilst the second hose is hand operated. A water injection system is included for lubricating the flow of emulsion through the delivery hoses and a control system is used to regulate the speed of the pumps and hose reel.
Ammonium nitrate emulsion (ANE) is drawn from hopper 1 by progressive cavity pump 1 (PC1) at a flow rate of 100 kg/min measured with a coriolis flowmeter. A second stream of ANE is drawn from hopper 2 by a second progressive cavity pump, PC2, at a flow rate of 300 kg/min measured by a coriolis flowmeter. The flow rates of the two streams are monitored on the control system and the pump speeds adjusted to obtain the correct flow rates. A gasser solution comprising 30% wt sodium nitrite is supplied at a rate of 750 g/min to the ANE stream from PC1 by means of a gasser delivery system comprising a supply tank, pump and flowmeter. Six 25 mm diameter SMX static mixers disperse the gasser solution as droplets in the emulsion stream. Three way valves are positioned to direct the emulsion streams from PC1 and PC2 to a series of three 75 mm diameter helical static mixers producing a structure containing discrete regions of unsensitized emulsion and regions in which the emulsion includes droplets of gasser solution. A water injector is located downstream of the helical mixers to lubricate the flow of emulsion down a 50 mm internal diameter hose. The hose is lowered down a 20 m deep, 230 mm diameter blasthole by means of a motorized hose reel. PC1, PC2 and the gassing system are started simultaneously, and after a period of 10 seconds the hose reel begins withdrawing the hose at a steady rate, keeping the end of the hose below the surface of the rising column of explosive. The explosive is loaded to a collar height of 6 m and allowed to gas for 1 hour before stemming. The charge is initiated with a conventional 400 g primer.
A mobile manufacture and delivery platform is used for manufacture and delivery of an explosive with non-random void distribution in accordance with Specific Embodiment 2. The MMDP includes a raw material hopper for ammonium nitrate emulsion, a pump to convey the emulsion, a flow splitter for splitting the flow of emulsion into two streams, a gassing system for delivering gasser solution to one of the emulsion streams, static mixers to disperse the gasser solution into one of the streams, a flowmeter to measure the flow rate of the two emulsion streams, a valve to control the flow-rate of the two emulsion streams, helical mixers for blending the two emulsion streams, a water injection system for lubricating the flow of emulsion through a delivery hose, a motorized hose reel to lower and retract the hose, and a control system to regulate the speed of the pumps and hose reel.
Ammonium nitrate emulsion (ANE) is drawn from a hopper by a progressive cavity pump at a flow rate of 250 kg/min. The flow from the pump is split in a T-shaped piece to produce two separate flow streams. One stream remains unsensitized and the second stream is sensitized by chemical gassing. The flow rate of each stream is measured with an ultrasonic flowmeter, and a globe valve located in the unsensitized emulsion line is adjusted such that the flow of unsensitized emulsion is 190 kg/min, resulting in a flow of 60 kg/min of emulsion to be sensitized. A chemical gassing system, consisting of a supply tank, triplex plunger pump and flowmeter is used to supply a 33% sodium nitrite gassing solution at a rate of 500 g/min to the 60 kg/min emulsion stream. The sodium nitrite solution is dispersed as droplets in the emulsion stream using a series of eight 25 mm diameter SMX static mixers. These mixers also provide resistance to the flow of emulsion, allowing the flow ratio of the two streams to be controlled by means of a single valve located in the unsensitized emulsion line.
The two emulsion streams are blended in a series of four helical static mixers with a diameter of 50 mm to produce a structure containing discrete regions of unsensitized emulsion and regions in which the emulsion includes droplets of gasser solution. The blended product is conveyed to a 15 m deep, 230 mm diameter blasthole by means of a 50 mm internal diameter hose mounted on a motorized hose reel with variable speed motor. The hose is lowered to the base of the blasthole and remains stationary for the first 10 seconds of delivery. After 10 seconds the hose reel motor is activated to withdraw the hose at a constant rate, maintaining the end of the hose below the surface of the rising column of explosive. The explosive is loaded to a collar height of 6 m and allowed to gas for 1 hour before stemming. The charge is initiated with a conventional 400 g primer.
A mobile manufacture and delivery platform is used for manufacture and delivery of an explosive with non-random void distribution in accordance with Specific Embodiment 3. The MMDP includes raw material hoppers for ammonium nitrate emulsion, two pumps for producing two streams of emulsion, flowmeters for measuring the emulsion flow rates, a gasser delivery system for supplying gasser solution to one of the emulsion streams, static mixers for dispersing the gasser, two hoses for conveying the two emulsion streams to the blasthole, a hose reel to lower and retract the two hoses, a water injection system to lubricate the two hoses and a blending head connected to the ends of the hoses containing helical static mixers for blending the two emulsions in the blasthole.
Ammonium nitrate emulsion (ANE) is drawn from hopper 1 by progressive cavity pump 1 (PC1) at a flow rate of 40 kg/min. A second stream of ANE is drawn from hopper 2 by a second progressive cavity pump, PC2, at a flow rate of 120 kg/min. Pumps are pre-calibrated to determine the operating speed required to achieve the desired flow-rates. A chemical gassing system, consisting of a supply tank, pump and flowmeter is used to supply a 30% sodium nitrite gassing solution at a rate of 300 g/min to the emulsion stream delivered by PC1. The sodium nitrite solution is dispersed as droplets in the emulsion stream using a series of eight 25 mm diameter SMX static mixers. Emulsion streams from PC1 and PC2 are delivered down separate 25 mm diameter hoses lubricated with water at rates of 0.5 and 1.5 kg/min, respectively. A blending head is connected to the outlets of the emulsion hoses and contains a series of five 50 mm diameter helical static mixers to produce a structure containing discrete regions of unsensitized emulsion and regions in which the emulsion includes droplets of gasser solution. The hoses are simultaneously lowered to the base of a 10 m deep, 200 mm diameter blasthole by means of a dual hose reel. PC1, PC2 and the gasser pump are started simultaneously, and the emulsions are delivered down the separate hoses and blended at the hose outlets in the blending head, initially positioned at the base of the blasthole. After 20 seconds of loading, the hose reel motor is started and the hoses are withdrawn simultaneously at a constant rate, with the outlet of the blending head remaining below the surface of the rising column of explosive. The explosive is loaded to a collar height of 4 m and is allowed to gas for 1 hour before stemming and initiating with a standard 400 g primer.
The mobile manufacture and delivery platform described in Example 1 is modified to incorporate a Y-piece static mixer inlet in accordance with Specific Embodiment 4. The Y-piece contains inlets for sensitized and unsensitized emulsion and produces a single output with the components separated by a central baffle to prevent unintended mixing of the two streams prior to entering the helical static mixers. The Y-piece baffle is aligned perpendicular to the first helical mixer element blade.
Ammonium nitrate emulsion (ANE) is drawn from hopper 1 by progressive cavity pump 1 (PC1) at a flow rate of 20 kg/min measured with a coriolis flowmeter. A second stream of ANE is drawn from hopper 2 by a second progressive cavity pump, PC2, at a flow rate of 60 kg/min measured by a coriolis flowmeter. The flow rates of the two streams are monitored on the control system and the pump speeds adjusted to obtain the correct flow rates. A gasser solution comprising 30% wt sodium nitrite is supplied at a rate of 100 g/min to the ANE stream from PC1 by means of a gasser delivery system comprising a supply tank, pump and flowmeter. Six 25 mm diameter SMX static mixers disperse the gasser solution as droplets in the emulsion stream. Three way valves are positioned to direct the emulsion streams from PC1 and PC2 to a Y-piece connected to a series of three 25 mm diameter helical static mixers producing a structure containing discrete regions of unsensitized emulsion and regions in which the emulsion includes droplets of gasser solution. A water injector is located downstream of the helical mixers, delivering water at a rate of 0.8 kg/min to lubricate the flow of emulsion down a 25 mm internal diameter hose. The hose is lowered by hand down a 10 m deep, 150 mm diameter blasthole. PC1, PC2 and the gassing system are started simultaneously, and after a period of 20 seconds the hose is withdrawn by the operator at a steady rate, keeping the end of the hose below the surface of the rising column of explosive. The explosive is loaded to a collar height of 4 m and allowed to gas for 1 hour before stemming. The charge is initiated with a conventional 400 g primer.
The mobile manufacture and delivery platform described in Example 2 is modified to incorporate a Y-piece to provide concentric streams of sensitized and unsensitized emulsion. The Y-piece contains inlets for sensitized and unsensitized emulsion and produces a single output with a core of sensitized emulsion and an annulus of unsensitized emulsion. The Y-piece is connected to the delivery hose, and the helical static mixers are relocated to a blending head mounted on the end of the delivery hose for blending the emulsion.
Ammonium nitrate emulsion (ANE) is drawn from a hopper by a progressive cavity pump at a flow rate of 250 kg/min. The flow from the pump is split in a T-shaped piece to produce two separate flow streams. One stream remains unsensitized and the second stream is sensitized by chemical gassing. The flow rate of each stream is measured with an ultrasonic flowmeter, and a globe valve located in the unsensitized emulsion line is adjusted such that the flow of unsensitized emulsion is 190 kg/min, resulting in a flow of 60 kg/min of emulsion to be sensitized. A chemical gassing system, consisting of a supply tank, triplex plunger pump and flowmeter is used to supply a 30% sodium nitrite gassing solution at a rate of 500 g/min to the 60 kg/min emulsion stream. The sodium nitrite solution is dispersed as droplets in the emulsion stream using a series of eight 25 mm diameter SMX static mixers. These mixers also provide resistance to the flow of emulsion, allowing the flow ratio of the two streams to be controlled by means of a single valve located in the unsensitized emulsion line.
The two emulsion streams are combined in a Y-piece to produce a single stream with an inner core of emulsion containing droplets of gasser solution and an annulus of unsensitized emulsion. The stream of emulsion is conveyed to a 15 m deep, 230 mm diameter blasthole by means of a 50 mm internal diameter hose mounted on a motorized hose reel with variable speed motor. A blending head containing four 50 mm diameter helical static mixers is located on the hose outlet to create a product structure containing discrete regions of unsensitized emulsion and regions in which the emulsion includes droplets of gasser solution. The hose is lowered to the base of the blasthole and remains stationary for the first 10 seconds of delivery. After 10 seconds the hose reel motor is activated to withdraw the hose at a constant rate, maintaining the end of the hose below the surface of the rising column of explosive. The explosive is loaded to a collar height of 6 m and allowed to gas for 1 hour before stemming. The charge is initiated with a conventional 400 g primer.
The following information is taken from the disclosure of PCT/AU2012/001527. This information should be read in this context. For example, in this section when reference is made to “the invention” or “the present invention”, this is a reference to the invention described in PCT/AU2012/001527.
In accordance with a first embodiment of the invention there is provided an explosive composition comprising a liquid energetic material and sensitizing voids, wherein the sensitizing voids are present in the liquid energetic material with a non-random distribution, and wherein the liquid energetic material comprises (a) regions in which the sensitizing voids are sufficiently concentrated to render those regions detonable and (b) regions in which the sensitizing voids are not so concentrated, wherein the explosive composition does not contain ammonium nitrate prill.
The explosive composition of the present invention is defined with reference to its internal structure. The liquid energetic material comprising (a) regions in which the sensitizing voids are sufficiently concentrated to render those regions detonable and (b) regions in which the sensitizing voids are not so concentrated, rendering different detonation characteristics. Thus, a charge made up (entirely) of liquid energetic material in which the sensitizing voids are sufficiently concentrated to render the liquid energetic material detonable will have different detonation characteristics when compared with a charge made up (entirely) of liquid energetic material in which the sensitizing voids are not so concentrated. The (regions of) liquid energetic material having lower concentration of sensitizing voids (i.e. those regions “in which the sensitizing voids are not so concentrated” may be per se detonable but with reduced detonation sensitivity when compared with (those regions of) liquid energetic material including higher concentration of sensitizing voids. Alternatively, (the regions of) liquid energetic material having lower concentration of sensitizing voids may be per se non-detonable.
Herein differences in detonation sensitivity relate to the intrinsic sensitivity of the individual regions, and also concentration of the sensitizing voids present within the regions, of liquid energetic material. It is generally accepted that the sensitivity of an energetic material to shock wave initiation is governed by the presence of the sensitizing voids. Shock-induced void collapse due to application of a shock wave is a typical mechanism for hot spot formation and subsequent detonation initiation in energetic materials. The generation of the shock induced hotspots, or regions of localized energy release, are crucial processes in shock initiation of energetic materials. The effectiveness of the shock initiation further depends on the amplitude and duration of the shock wave.
It is to be appreciated that the explosive composition of this first embodiment is distinguished from conventional explosive compositions that are formulated by blending sensitizing voids with a liquid energetic material to provide a sensitized explosive product. In that case the voids will be distributed in the liquid energetic material with a random distribution (no amount of mixing will result in a uniform (non-random) spaced distribution of voids). With this random arrangement of voids it may be possible to identify regions in which voids are present in greater concentrations than in others, but the void distribution is nevertheless random in character and there is no structural or systematic consistency within the energetic material with respect to void distribution.
This is to be contrasted with the present invention in which the voids are present with a non-random distribution to provide regions that are void rich and regions that are void deficient. In accordance with this aspect of the invention the voids are present in the liquid energetic material as clusters, and in this respect the explosive compositions of the invention have some structural and systematic consistency with respect to the organization of the voids. In the context of the present invention the term “clusters” is intended to denote a deliberate, grouped arrangement of voids. This arrangement is non-random in character and is not arbitrary in nature.
In relation to this first embodiment of the invention it will be appreciated that regions of liquid energetic material having a high concentration of voids, i.e. including clusters of voids, will per se have different detonation characteristics form regions which have a lower concentration of voids, or no voids at all. It is a requirement of the invention that the explosive composition includes regions in which the sensitizing voids are sufficiently concentrated to render those regions detonable, and this means that those regions would be per se detonable. In other words an explosive composition having a bulk structure corresponding to that of these regions would be detonable in its own right. As voidage influences detonation characteristics, it follows that those regions in the explosive compositions of the invention that have a lower concentration of voids will per se exhibit different detonation characteristics from those regions in which the voids are more highly concentrated. In accordance with the invention it has been found that providing in a single formulation regions of liquid energetic material that per se have different detonation characteristics allows the bulk detonation characteristics of the explosive composition to be influenced and controlled.
In accordance with a second embodiment of the invention regions having different detonation characteristics due to void concentrations can be provided by the use of distinct liquid energetic materials that are sensitized to different extents and that are combined to form an explosive composition. In this embodiment the explosive composition comprises regions of a first liquid energetic material and regions of a second liquid energetic material, wherein the first liquid energetic material is sensitized with sufficient sensitizing voids to render it detonable and wherein the second energetic liquid has different detonation characteristics from the sensitized first liquid energetic material. The (base) liquid energetic materials may be the same or different, although typically the same liquid energetic material is used. When different they will have different physical and chemical properties, such as density and composition.
In embodiments of the invention the explosive compositions of the present invention do not need to rely on ammonium nitrate prill or like material to modify the blasting properties of the explosive composition. Rather, the blasting properties of the explosive composition are directly attributable to the individual regions (and possibly to the liquid energetic material used in those regions where multiple energetic liquids are employed) from which the composition is made up. In accordance with the present invention this approach allows explosive compositions to be formulated that have energy release characteristics (in terms of shock and heave energies) that are at least comparable to conventional prill-containing explosive formulations.
In an embodiment the explosive compositions of the invention do not need to contain any solid oxidiser components or fuels, such as prill, and this means that they can be pumped with relative ease. Thus, related to the first embodiment of the invention, the invention provides an explosive composition consisting of, or consisting essentially of, a liquid energetic material and sensitizing voids, wherein the sensitizing voids are provided in the liquid energetic material with a non-random distribution, and wherein the liquid energetic material comprises (a) regions in which the sensitizing voids are sufficiently concentrated to render those regions detonable and (b) regions in which the sensitizing voids are not so concentrated.
Related to the second embodiment of the invention, the explosive composition may consist of, or consist essentially of, regions of a first liquid energetic material and regions of a second liquid energetic material, wherein the first liquid energetic material is sensitized with sufficient sensitizing voids to render it detonable and wherein the second energetic liquid has different detonation characteristics from the sensitized first liquid energetic material.
In these embodiments the expressions “consisting of” and variations thereof are intended to mean that the explosive composition contains the stated components and nothing else. The expressions “consisting essentially of” and variations thereof are intended to mean that the explosive composition must contain the stated components but that other components may be present provided that these components do not materially affect the properties and performance of the explosive composition.
The present invention also provides a method of producing an explosive composition, the method comprising providing sensitizing voids in a liquid energetic material, wherein the sensitizing voids are provided in the liquid energetic material with a non-random distribution, and such that the liquid energetic material comprises (or consists of or consists essentially of) (a) regions in which the sensitizing voids are sufficiently concentrated to render those regions detonable and (b) regions in which the sensitizing voids are not so concentrated.
Consistent with the second embodiment of the invention, there is also provided a method of producing an explosive composition, the method comprising (or consisting of or consisting essentially of) combining together a first liquid energetic material and a second liquid energetic material to provide regions of the first liquid energetic materials and regions of the second liquid energetic material, wherein the first liquid energetic material is sensitized with sufficient sensitizing voids to render it detonable and wherein the second energetic liquid has different detonation characteristics from the sensitized first liquid energetic material.
As another variant, the present invention enables explosive compositions to be formulated with reduced quantities of ammonium nitrate prill when compared with conventional prill-containing explosives, whilst achieving the same detonation energy balance as such conventional explosives. Accordingly, the present invention also provides an explosive composition comprising a liquid energetic material and sensitizing voids, wherein the sensitizing voids are present in the liquid energetic material with a non-random distribution, wherein the liquid energetic material comprises (a) regions in which the sensitizing voids are sufficiently concentrated to render those regions detonable and (b) regions in which the sensitizing voids are not so concentrated, and wherein the composition further comprises no more than 25 weight %, preferably no more than 15 weight % and, most preferably, no more than 10 weight %, of solid ammonium nitrate (as AN prill or ANFO) based on the total weight of composition. This represent somewhere between 20 to 50% of the amount of solid AN or ANFO used in conventional explosive compositions.
In this embodiment the solid (prill) component should generally be provided in higher density regions of the liquid energetic material making up the explosive composition, i.e. those regions that do not include sensitizing voids or a reduced level of sensitizing voids when compared with other regions that (are designed to) have a higher concentration of sensitizing voids. For example, this embodiment may be implemented by premixing solid AN prill or ANFO with an unsensitized liquid energetic material prior to blending the unsensitized liquid energetic material with a sensitized liquid energetic material consistent with the general principles underlying the invention.
In this embodiment the detonation characteristics of the explosive composition can be tailored in accordance with the underlying principles of the invention by controlling how voids are placed and concentrated within the liquid energetic material so it is possible to achieve an intended detonation energy outcome without needing to include as much prill as one would do normally. The inclusion of relatively small amounts of AN prill may also be applied to influence detonation characteristics, however. Some applications may benefit from the generation of additional energy from decomposition of the solid component or/and utilizing its free oxygen in further reactions with available fuels. Inclusion of the solid component in void-free regions of liquid energetic material may lead to an increase in the total energy of the composition through reduction of the water content in those regions of liquid energetic material.
The present invention also provides a method of varying the energy release characteristics of a first liquid energetic material sensitized with sufficient sensitizing voids to render it detonable which comprises formulating an explosive composition comprising (or consisting of or consisting essentially of) regions of the first liquid energetic material and regions of a second liquid energetic material, wherein the second energetic liquid has different detonation characteristics from the sensitized first liquid energetic material.
The present invention also provides a method of (commercial) blasting using an explosive composition in accordance with the present invention. The explosive composition is used in exactly the same manner as conventional explosive compositions. The explosive compositions of the invention are intended to be detonated using conventional initiating systems, for example using a detonator and a booster and/or primer.
The context of use of the explosive composition of the present invention will depend upon the blasting properties of the composition, especially with regard to the heave and shock energies of the composition. It will be appreciated however that it is envisaged that, in view of their desirable energy release characteristics, the present invention will provide explosive compositions that can be used instead of conventional ANFO or AN prill-containing formulations. Explosive compositions of the invention may have particular utility in mining and quarrying applications.
Herein the term “liquid energetic material” is intended to mean a liquid explosive that has stored chemical energy that can be released when the material is detonated. Typically, a liquid energetic material would require some form of sensitization to render it per se detonable. Thus, the term excludes materials that are inherently benign and that are non-detonable even if sensitized, such as water. It should be noted however that this does not mean that each liquid energetic material in the explosive compositions of the invention are in fact sensitized. Indeed, in embodiments of the invention, one of the liquid energetic materials is sensitized and another liquid energetic material is not sensitized at all. That said, in other embodiments one of the liquid energetic materials is sensitized and another liquid energetic material is sensitized to a lesser extent.
The energetic materials used in the invention are in liquid form, and here specific mention may be made of explosive emulsions, water gels and slurries. Such emulsions, water gels and slurries are well known in the art in terms of components used and formulation.
In the context of the present invention, the term “explosive composition” means a composition that is detonable per se by conventional initiation means at the charge diameter being employed.
Throughout this specification and the claims which follow, unless the context requires otherwise, the word “comprise”, and variations such as “comprises” and “comprising”, will be understood to imply the inclusion of a stated integer or step or group of integers or steps but not the exclusion of any other integer or step or group of integers or steps.
The reference in this specification to any prior publication (or information derived from it), or to any matter which is known, is not, and should not be taken as an acknowledgment or admission or any form of suggestion that that prior publication (or information derived from it) or known matter forms part of the common general knowledge in the field of endeavour to which this specification relates.
FIGS. 1-8 of PCT/AU2012/001527 are included as part of the present specification are included as part of the present specification and clearly identified as such in the legend to the figure.
In accordance with the present invention it has been found that the detonation characteristics of a void sensitized liquid energetic material can be controlled by controlling how the voids are arranged within the liquid energetic material. In particular it has been found that the ratio of heave energy to shock energy delivered by detonation of liquid energetic materials sensitized with voids can be significantly increased, compared with existing void sensitized “all liquid” energetic materials, by controlling how the voids are distributed with respect to each other. It is also possible to achieve a high heave to shock energy ratio whilst maintaining higher total energy densities than is available from conventional “all liquid” systems.
Prior to the present invention much has been reported on the use of different types of voids and voidage levels, but there is not believed to have been any systematic investigation of the effect of relative void spatial distribution. Existing void sensitized liquid energetic materials have a similar (random) spatial distribution of the voids with respect to each other. Only by using voids which provide fuel, such as expanded polystyrene, and with void diameters of 500 μm or more, have higher heave energies been achieved. With the present invention unconventionally high ratios of heave to shock energies with voids sizes from 20 μm to 5 mm can be achieved, and high total energies similar to solid AN prill-containing formulations, can be achieved.
Without wishing to be bound by theory, the mechanisms involved when an explosive composition of the invention is initiated are believed to be as follows. Distribution of the explosive energy between shock and heave is governed by the speed of reactions within the individual sensitized and unsensitized regions. The chemical reactions within the hot spots are fast and exothermic and thus enable detonations by large number of interconnected, small thermal explosions. The number and size of the hot spots controls the sensitivity and speed of detonation reactions within the sensitized region. In this way the sensitized region contributes to the magnitude of the shock energy output. The insufficient number or total absence of hot spots leads to relatively slow reactions (burning) in unsensitized region of energetic liquid. The grain burning mechanism controls the rate of energy release within unsensitized regions of the energetic material. The process hence determines output of the heave energy. Importantly, in accordance with the invention, the energy release characteristics of the explosive composition can be controlled and tailored by varying the void distribution, void volume, the combination of liquid energetic components used and/or the arrangement of the liquid energetic components within the bulk of the explosive composition. In turn, this enables the detonation properties of the explosive composition to be tailored to particular rock/ground types and to particular mining applications.
The present invention may be of particular interest when applied to the use of emulsion explosives as liquid energetic materials. Emulsion-based bulk explosives do not have blasting characteristics, such as velocity of detonation (VOD), equivalent to conventional ANFO or AN prill-containing explosives. However, emulsion explosives do have desirable properties in terms of water resistance and the ability to be pumped. Accordingly, emulsion-based explosive compositions of the present invention may be used as an alternative to ANFO and AN-containing products. This will allow such conventional explosives compositions to be replaced with products that are emulsion-only based. Accordingly, the present invention also provides the use of an emulsion explosive composition in accordance with the present invention in a blasting operation as an alternative to ANFO or AN-containing product.
In this context the emulsion explosives are typically water-in-oil emulsions comprising a discontinuous oxidizer salt solution (such as ammonium nitrate) dispersed in a continuous fuel phase and stabilized with a suitable emulsifier. Sensitization is achieved in conventional manner by inclusion of “voids” such as gas bubbles or micro-balloons, e.g. glass or polystyrene micro-balloons. This will influence the density of the emulsion.
Central to the present invention is the arrangement with which voids are distributed within a liquid energetic material. Thus, the explosive compositions of the present invention include regions that are void rich (i.e. relatively concentrated) and regions that are void deficient (i.e. not so concentrated), these regions per se having different detonation characteristics. Combining such regions results in a bulk product having novel detonation characteristics as compared to the detonation characteristics of the individual regions that are present. As will become apparent there is great scope for modifying the internal structure of the bulk product based on its constituent components/regions and in turn this advantageously provides great scope for tailoring the explosive characteristics of the product.
In accordance with the present invention it may be possible to achieve one or more of the following practical benefits otherwise not attainable with a homogeneous emulsion-only void sensitized explosive compositions:
When compared with solid AN-containing formulations, explosive compositions of the invention that are prill-free offer the following benefits:
In the first embodiment of the invention the explosive composition comprises a liquid energetic material and sensitizing voids, wherein the sensitizing voids are present in the liquid energetic material with a non-random distribution, and wherein the liquid energetic material comprises (a) regions in which the sensitizing voids are sufficiently concentrated to render those regions detonable and (b) regions in which the sensitizing voids are not so concentrated. In this embodiment the internal structure of the explosive composition is characterized by the distribution of voids, the volume ratio of the various regions and the arrangement of the regions. The void distribution may broadly be understood with reference to
In another (second) embodiment of the invention the explosive composition comprises regions of a first liquid energetic material and regions of a second liquid energetic material, wherein the first liquid energetic material is sensitized with sufficient sensitizing voids to render it detonable and wherein the second energetic liquid has different detonation characteristics from the sensitized first liquid energetic material. It will be appreciated that this embodiment is related to the first embodiment in that in the second embodiment individual liquid energetic materials are combined to provide the regions having the requisite void concentrations referred to in the first embodiment.
With respect to the second embodiment of the invention, the (internal) structure of the explosive composition is characterized by the volume ratio of each component (liquid energetic material) and the structural arrangement/distribution of the components relative to each other. In the explosive compositions of this embodiment the two components are generally present as (discrete) regions.
In accordance with this embodiment the first and second liquid energetic materials have different detonation characteristics, such as VOD and detonation sensitivity. In one embodiment the first and second liquid energetic materials (e.g. emulsion explosives) are derived from the same base source (e.g. emulsion). For example, in this case, the first emulsion may be produced by void sensitizing a base emulsion, thereby reducing its density, and the second emulsion may be the base emulsion itself. In this case the explosive composition will include discrete regions of basic (unsensitized) emulsion and regions of the sensitized emulsion. The density and blasting characteristics of the resultant explosive composition will be determined and influenced by the individual components from which the composition is formed.
Advantageously, in this second embodiment of the invention the make up and structural characteristics of the explosive composition may be varied in a number of ways and this may provide significant flexibility in terms of achieving particular blast outcomes that have otherwise not been achievable using conventional emulsion-based void sensitized explosive products. Thus, in the embodiment described, where an unsensitized emulsion is provided in combination with a sensitized emulsion, numerous possibilities exist within the spirit of the present invention. The following are given by way of example. It will be appreciated that combinations of the following variants may be employed.
It will be appreciated from this that the formulation flexibility associated with the present invention allows the production of explosive compositions that have detonation characteristics, such as VOD, to be substantially different from homogeneous emulsion-only void sensitized explosive products having similar composition in terms of liquid energetic material and void sensitization.
The sensitizing voids may be gas bubbles, glass micro-balloons, plastic micro-balloons, expanded polystyrene beads, or any other conventionally used sensitizing agent. The density of the sensitizing agent is typically below 0.25 g/cc although polystyrene spheres may have a density as low as 0.03-0.05 g/cc, and the voids generally have mean diameters in the range 20 to 2000 μm, for example in the range 40 to 500 μm.
Noting the scope for variation in composition formulation that exists, it would in fact be possible to provide a comprehensive suite of explosive compositions tailored to meet different blasting requirements using only a limited number of base emulsion formulations. In turn this may lead to more streamlined logistics, while at the same time possibly lead to lower formulation and operational costs.
Furthermore, the present invention may render useful products that have previously been thought to be unsuitable in the explosives context. For example, by using ammonium nitrate as melt grade only, a range of previously unacceptable ammonium nitrate sources could be used, leading to lower cost explosives.
The present invention also provides a method of (commercial) blasting using an explosive composition in accordance with the present invention. The explosive compositions of the invention are intended to be detonated using conventional initiating systems, for example comprising a detonator and a booster and/or primer. The present invention may be applied to produce explosive composition that detonate at a steady predetermined velocity, with a minimum VOD of 2000 m/s, for example from 2000-6000 m/s in either a confined bore hole, or under unconfined conditions. It will be appreciated that the VOD of an explosive composition in accordance with the invention will be less than the VOD of the component (or region) of the composition having the highest VOD. It is well known that the amount of shock energy at a given explosive density is proportional to the VOD, and as such, reduction in the VOD results in a decrease in shock energy and corresponding increase in heave energy.
Advantageously, the present invention may be used to provide an emulsion-based explosive composition that matches ANFO or an AN prill based product with respect to density and velocity of detonation. For example, if a commercially available product containing AN prill has a density of 1.2 g/cc, this same density could be achieved by using an explosive composition in accordance with the invention in which a non-sensitized emulsion having a density of 1.32 g/cc is used in combination with a void-sensitized emulsion having a density of 0.8 g/cc at a volume ratio of 78:22. The same density could of course be achieved using different volume proportions of emulsions having different densities. For example, a density of 1.32 g/cc could be achieved using the following combinations of densities and volume ratios for the non-sensitized and sensitized emulsions respectively: 1.32 g/cc and 1.0 g/cc at 67:33; 1.32 g/cc and 0.9 g/cc at 73:27; and 1.32 g/cc and 0.8 g/cc at 78:22. The VOD of each explosive composition will be different, and a target VOD may be achieved by varying the volume ratio and density of the emulsion components whilst maintaining density matching with the prill-containing product. In proceeding in this way it is possible to provide emulsion-based explosive compositions that offer similar blasting performance to prill-based products.
Explosive compositions in accordance with the present invention may be made by blending together a first liquid energetic material and a second liquid energetic material to provide regions of the first liquid energetic materials and regions of the second liquid energetic material, wherein the first liquid energetic material is sensitized with sufficient sensitizing voids to render it detonable and wherein the second energetic liquid has different detonation characteristics from the sensitized first liquid energetic material. Blending of the individual liquid energetic materials may take place during loading into a blasthole but this is not essential and blending may be undertaken in advance provided that delivery into a blasthole does not disrupt the intended structure of the explosive composition. The liquid energetic materials used may be the same or different.
In an embodiment of the invention an explosive composition may be prepared by mixing of streams of individual components using a static mixer (see
By way of example, in the fluid stream (1), a void-free ammonium nitrate emulsion (ANE1) is mixed in line with an aqueous solution of sodium nitrite in a gasser mixing point using an arrangement of SMX type static mixers. After completion of the gassing reaction the emulsion stream (1) will have a particular density. The second fluid stream (2) may consist of a void-free ammonium nitrate emulsion having a higher density than the gassed emulsion stream (1).
The inter-changeable mixing head is comprised of two parts. The first part has two separate inlet channels for the entry of each emulsion stream and a baffle just before the entrance to the first static mixer element to ensure separation of the individual streams in the mixing section. The inter-changeable mixing head is 50 mm diameter and length of 228 mm.
A helical static mixer (having 3 elements; see
Embodiments of the present invention are illustrated with reference to the following non-limiting examples.
In the absence of AN prill, bulk emulsion explosives rely on the inclusion of voids for sensitization. In such emulsions the oxidizer salt used is typically ammonium nitrate. When an ammonium nitrate emulsion (ANE) is sensitized with voids, for example by chemical gassing or by using micro-balloon (mb) inclusion, the void size is approximately 20-500 μm in diameter. When voids are used to sensitize such emulsion explosives they reduce the formulation density. However, homogeneous sensitization of emulsions with voids will result in much higher velocity of detonation (VOD) than corresponding formulations of a similar density containing AN prill.
This example details explosive compositions made up of two emulsion components: a non-sensitized ammonium nitrate emulsion (n-ANE) and a sensitized ammonium nitrate emulsion (s-ANE). The non-sensitized emulsion in this example has an ammonium nitrate concentration of approximately 75 wt % and a density of approximately 1.32 g/cc. The s-ANE has an ammonium nitrate concentration of approximately 75 wt % and a variable density from 0.8-1.2 g/cc using either chemical gassing or micro-balloons of a diameter of approximately 40 p.m. Various explosive compositions in accordance with the invention can be formed by blending these emulsions and by adjusting the ratio of n-ANE:s-ANE in the formulation. As the ratio is adjusted from the extremes of 100% n-ANE to 100% s-ANE in a 200 mm diameter cardboard cylinder, the VOD ranges from a failure to detonate for the non-sensitized emulsion to over 6000 m/s for 100% s-ANE. However, the ability to isolate discrete regions of s-ANE (or n-ANE) within a bulk charge of n-ANE (or s-ANE) allows a geometric formulation variable to control detonation velocity and blasting characteristics between these extremes.
The method of manufacturing explosive compositions in accordance with the invention is based on blending two liquid energetic materials. The first phase is conventionally sensitized with voids, the second phase with no or very few added voids, the blending being such that the two phases remain largely distinct from each other, and the diameter, sheet thickness, etc. of the distinct phases are typically in the range from 0.2 mm to 100 mm.
Examples of Homogeneous s-ANE Charges
To identify how homogeneous s-ANE would perform without any n-ANE inclusions, a series of control charges were measured for VOD. The control shots contained ammonium nitrate emulsion and plastic Expancel micro-balloons of approximate 40 μm average diameter. The emulsion and micro-balloons were mixed to form a homogeneous blend ranging in density from 0.8 g/cc to 1.2 g/cc based on the amount of micro-balloons used. The VOD results can be seen in Table 1 below. A standard VOD measurement technique was used in which compositions were submitted for a detonation test in various unconfined diameters. Charges were detonated using Pentolite primers that were initiated with a No8 industrial strength detonator. The velocity of detonation (VOD) of the charges was measured by utilising a micro-timer unit and optical fibres.
As the density increased from 0.8 to 1.2 g/cc the VOD increased from 4.5-6.3 km/s. Clearly, the homogeneous sensitization of emulsion with 40 μm diameter voids produces an emulsion explosive of higher velocity of detonation at increasing densities as would be expected.
In accordance with the present invention it is possible to reduce the VOD of these emulsion only explosives for each of the above densities, using the same size voidage, i.e. 40 μm diameter micro-balloons. To do this, regions of non-sensitized emulsion (n-ANE) were introduced into the sensitized emulsion to reduce the bulk VOD. The non-sensitized ammonium nitrate emulsion has a density of approximately 1.32 g/cc and consequently increases the overall density of the charge upon simple addition. Therefore to compare charges of equal density to the controls, sensitized emulsion (s-ANE) density must be sufficiently low that subsequent to n-ANE inclusion, the overall charge density is that desired.
The experimental arrangement is shown schematically in
The charge labeled M1.0,S0.9 in Table 2 below has an overall charge density of 1.0 g/cc, and contains two discrete emulsion phases as per the present invention. A continuous phase of s-ANE (emulsion+micro-balloons, density of 0.9 g/cc) occupying a total of 76.2% of the charge volume, and within this continuous phase are dispersed regions of n-ANE (density of 1.32 g/cc) which occupy the remaining 23.8% of the charge volume. For the purposes of laboratory testing these dispersed regions are in fact 120 ml cardboard cups filled with the n-ANE and placed randomly within the continuous emulsion, thus allowing a physical boundary for isolation of discrete emulsion phases. The combined density of the s-ANE and n-ANE in the charge was 1.0 g/cc. However, the VOD was found to be 4.9 km/s. This is a 13.2% reduction in VOD compared with control 1.0. Indeed, the VOD of charge M1.0,S0.9 is closer to the VOD of the Control 0.9 detailed above in Table 1 which is the same density as the continuous emulsion phase of this charge.
The charge labeled M1.0,S0.8 has an overall charge density of 1.0 g/cc, and a continuous s-ANE of 0.8 g/cc (61.5 vol %). Again, the charge has distributed cups (120 ml each) of n-ANE (38.5 vol %). The VOD of this charge was found to be 4.2 km/s, which is a 25% reduction in VOD compared to control 1.0. Once again the VOD for charge M1.0,S0.8 more closely matches the control shot at the same density as the continuous emulsion phase, i.e. Control 0.8 (Table 1) 4.5 km/s.
Also shown in Table 2 is the VOD for heavy ANFO (HANFO 1.0). This heavy ANFO is a homogeneous blend of emulsion (23 wt %) and ANFO (77 wt %), and as such does not have discrete continuous or dispersed emulsion phases as described for the mixtures of emulsion systems in accordance with the present invention. However, similar to the mixtures of emulsion and control 1.0 charges the heavy ANFO, HANFO 1.0, also has an overall charge density of 1.0 g/cc. Heavy ANFO charges rely on porous nitropril for sensitization, and the resulting VOD recorded was found to be 3.6 km/s. The last charge listed in Table 2 gives the results for VG100 which consists of emulsion (99.62 wt %) homogeneously mixed with expanded polystyrene (EPS, 0.38 wt %) of approximately 4 mm diameter for sensitization. As with heavy ANFO, the emulsion and expanded polystyrene are a homogeneous blend throughout the bulk charge and therefore have no discrete dispersed or continuous phases. The VOD for this product was found to be 3.6 km/s.
An important feature of the above charges is that the Control 1.0, M1.0,S0.9 and M1.0,S0.8 charges all have the same total quantity of emulsion and small 40 μm voids in the overall charges. Naturally, having equivalent formulation, they also have the same density, 1.0 g/cc. However, when the internal structure of the explosive charge contains two distinct phases of s-ANE and n-ANE, the VOD of the charge is reduced from the homogeneously mixed analogue such as Control 1.0. One important aspect of the invention is that emulsion only explosives utilizing small 40 μm voids can be formulated to have VOD characteristics of prill and EPS containing products.
Mixture of Emulsion (MOE) Charges of Overall Density 1.1 g/cc
As shown in Table 3 below, all charges have an overall density of 1.1 g/cc. The Control 1.1 was a single phase of s-ANE having a density of 1.1 g/cc. The VOD of this control shot was found to be 6.0 km/s. The charge labeled M1.1, S1.0 has a continuous s-ANE phase of density 1.0 g/cc occupying 68.4% of the total charge volume. The remaining volume of the charge was made up of n-ANE in 120 ml cups distributed throughout the charge. The VOD for charge M1.1,S1.0 was found to be 5.1 km/s. Similarly, charge M1.1, S0.9 was made up of a continuous emulsion phase of s-ANE having a density of 0.9 g/cc occupying 52.4% of the total charge volume and distributed therein 120 ml cups of n-ANE accounting for the remaining 47.6% of total charge volume. Charge M1.1, S0.9 was found to have a VOD of 4.6 km/s.
Charge M1.1,S0.8 was the first charge loaded with n-ANE as the continuous emulsion phase. Therefore, charge M1.1,S0.8 has non-sensitized continuous emulsion phase accounting for 58.8% of the total charge volume. Distributed within this charge was s-ANE having a density of 0.8 g/cc contained in 120 ml cups and accounting for the remaining 41.2 vol % of the total charge. The VOD for charge M1.1,S0.8 was found to be 3.2 km/s. This is a significant reduction to Control 1.1 charge. In addition this low VOD is also lower than heavy ANFO charge HANFO 1.1, thus confirming that mixtures of emulsions in accordance with the invention can achieve low detonation velocities down to levels not previously achievable by small 20-100 μm diameter voids, and comparable to nitropril containing emulsion products.
Mixture of Emulsion (MOE) Charges of Overall Density 1.2 g/cc
A series of charges all having an overall density of 1.2 g/cc is detailed in Table 4 below. The control charge was a homogenous blend of ammonium nitrate emulsion and micro-balloons of density 1.2 g/cc, and having a VOD of 6.3 km/s. The remaining charges detailed in Table 4 had a continuous emulsion phase of n-ANE. Charge M1.2,S1.0 had a continuous n-ANE phase accounting for 63.9% of the total charge volume. The s-ANE used had a density of 1.0 g/cc and was distributed within the n-ANE in 120 ml cups occupying remaining 36.1% of the total charge volume. Charge M1.2,S1.0 had a measured VOD of 4.3 km/s.
Charge M1.2,S0.9 included a continuous emulsion phase of n-ANE. This accounted for 73.1 vol % of the total charge. The remaining 26.9 vol % was made up of a s-ANE of density 0.9 g/cc. M1.2,S0.9 had a VOD of only 2.3 km/s. This low VOD could be close to failure as a consequence of such a high volume of n-ANE. Indeed M1.2,S0.8 with 78.0 vol % of n-ANE failed to initiate and over half of the test charge remained after attempted initiation with a 400 g Pentolite booster.
Although not experimentally measured, there are clearly opportunities to incorporate solid oxidizers, such as AN prill, in one or both of the phases to further fine tune the total energy available and the heave energy/shock energy balance. There are also clearly opportunities to incorporate sub-mm energetic solid fuels, such as aluminum, in one or both of the phases to further significantly enhance the heave energy while achieving exceptionally low shock energies.
This example serves as a baseline to demonstrate the features of the invention.
Experimental samples were prepared in a specially designed emulsion experimental rig. The corresponding process diagram is shown in
The inter-changeable mixing head is comprised of two parts. The first part has two separate inlet channels for the entry of each emulsion stream and a baffle just before the entrance to the first static mixer element to ensure separation of the individual streams in the mixing section. The inter-changeable mixing head is 50 mm diameter and length of 228 mm.
A Kenics static mixer (having 3 elements; see
The starting emulsion at a density of 1.32 g/cm3 was delivered by a progressive cavity pump at a rate of 3 kg/min. A 4% mass sodium nitrite solution was injected into the flowing emulsion stream at a rate of 16 g/min by means of a gasser (gear) pump and dispersed in a series of static mixers. 1 m long cardboard tubes with internal diameters ranging from 40 to 180 mm were loaded with emulsion and allowed to gas.
The density change of the gassing emulsion was determined in a plastic cup of known mass and volume. The emulsion was initially filled to the top of the cup and leveled off. As the gassing reaction progressed, the emulsion rose out of the top of the cup and was leveled off periodically and weighed. The density was determined by dividing the mass of emulsion in the cup by the cup volume. Charges were fired once the sample cup reached the target density of 1.22 g/cm3.
Charges larger than 70 mm were initiated with a single 400 g Pentex PPP booster, whist smaller charges were initiated with a 150 g Pentex H booster. Velocity of detonation (VOD) was determined using an MREL Handitrap VOD recorder. The VOD ranged from 2.9 km/s for the 70 mm diameter charge to 4.3 km/s at 180 mm. Charges smaller than 70 mm failed to sustain detonation. The results are shown in
This example demonstrates the performance of MOE25, i.e. a mixture of emulsion with 25% mass gassed and 75% ungassed emulsion.
MOE25 was prepared using the apparatus mentioned in Example 2. The base emulsion (density 1.32 g/cm3) was delivered by two progressive cavity pumps, PC1 and PC2. The base emulsion formulation was identical to Example 2 and was the same for both pumps. PC1 pumped ungassed emulsion at a flow rate of 4 kg/min. PC2 delivered emulsion at 1.3 kg/min with gasser (4% NaNO2 solution) injected by a gasser (gear) pump. The emulsion was blended by a static mixer consisting of three helical mixing elements and loaded into cardboard tubes with internal diameters ranging from 70 to 180 mm. The gassed emulsion target density was 0.99 g/cm3 providing an overall density of 1.22 g/cm3 for the mixture of gassed and ungassed emulsion.
Charges were initiated with a single 400 g Pentex PPP booster with VOD measured with an MREL handitrap VOD recorder. The VOD ranged from 2.5 km/s for the 90 mm charge to 3.7 km/s at 180 mm, a significant reduction relative to the regular gassed emulsion described in Example 2. Charges with diameters smaller than 90 mm failed to sustain detonation. The results are shown in
This example demonstrates the performance of MOE50, i.e. a mixture of emulsion with 50% mass gassed and 50% ungassed emulsion.
MOE50 was prepared using the apparatus mentioned in Example 2. The base emulsion (density 1.32 g/cm3) was delivered by two progressive cavity pumps, PC1 and PC2 and was identical to the previous two examples. PC1 pumped ungassed emulsion at a flow rate of 3 kg/min. PC2 delivered emulsion at 3 kg/min with gasser (4% NaNO2 solution) injected by a gasser (gear) pump. The void rich and void free emulsions were blended by a static mixer consisting of three helical mixing elements and loaded into cardboard tubes with internal diameters ranging from 70 to 180 mm. The gassed emulsion target density was 1.13 g/cm3 providing an overall density of 1.22 g/cm3 for the mixture of gassed and ungassed emulsion.
Charges were initiated with a single 400 g Pentex PPP booster with VOD measured with an MREL handitrap VOD recorder. The VOD ranged from 2.8 km/s for the 80 mm charge to 3.9 km/s at 180 mm. Charges with diameters smaller than 80 mm failed to sustain detonation. The results are shown in
The following information is taken from the disclosure of PCT/AU2012/001528. This information should be read in this context. For example, in this section when reference is made to “the invention” or “the present invention”, this is a reference to the invention described in PCT/AU2012/001528.
The present invention focuses on void-sensitized liquid energetic materials, such as emulsion explosives. This type of explosive formulation is well known and commonly used in the art. Emulsion explosives include voids distributed in a liquid energetic material, the voids rendering the explosive detonable. The voids may be in the form of gas bubbles, glass microballoons, plastic microballoons, expanded polystyrene spheres, and indeed any cavities that produce a low density region in the liquid explosive. For commercial mining explosives the average mean diameter of the voids can range from 25 microns to 500 microns. The lower end of void size is limited by the need for the void to act as an ignition point in the explosive and the upper end is limited by the need for the explosive to fully react. Preferably, an optimum voidage is incorporated in order to achieve satisfactory detonation propagation in terms of a critical diameter of the explosive charge and critical velocity of detonation. By using the minimum amount of voids it is possible to retain relatively high density of the resultant composition.
Typically, the total volume (voidage) occupied by the voids in the composition is at least 3% based on the total volume of the composition. Usually, the total volume of the voids is at least 10% by volume, for instance up to about 20% by volume. Inclusion of an amount of voids (or cavities) over and above the critical amount required for sensitization will unnecessarily reduce the density of the composition and lead to reduced energy-density of the resultant explosive material.
In the context of the present invention sensitizing voids may be gas bubbles, glass microballoons, plastic microballoons, expanded polystyrene beads, or any other material with a density below 0.25, with the voids having a mean diameter in the range 20 to 2000, preferably in the range 40 to 500 microns.
In accordance with the present invention it has been found that this type of explosive composition possesses structural features that can readily be tailored to influence detonation characteristics. The present invention provides a new way of defining the structure of an explosive material that comprises sensitizing voids distributed in a continuum of liquid energetic material. Specifically, in accordance with the present invention it has been found that the structure can be represented by a statistical/mathematical model. Moreover, it has been found that this model can be related to the bulk detonation properties of the explosive materials in terms of detonation and burning reactions. These reactions are related to the energy release profile associated with explosive materials in terms of the partitioning between shock and heave energies. Shock energy is related to detonation reactions and heave energy is related to (the efficiency of) burning reactions. This approach can be applied to characterize the structure and to understand the detonation behavior of known void sensitized liquid energetic materials. It may also be applied to characterize the structure and to understand/predict the detonation behavior of newly designed and formulated void sensitized liquid energetic materials.
In accordance with an embodiment of the invention it is possible to relate desirable bulk detonation properties of this type of explosives material to a statistical/mathematical model that represents the distribution of sensitizing voids within a (continuum of) liquid energetic material, and from that model to derive structural templates (in terms of void distribution) that will yield those detonation properties. This embodiment may therefore be regarded as a design tool for the formulation of void-sensitized liquid energetic materials.
The present invention uses what is referred to herein as a “distribution function” (DF) to characterize an explosives material in terms of its internal structure with respect to the distribution of sensitizing voids within a (continuum of) liquid energetic material. The “distribution function” (DF) is the fraction of liquid energetic material that is within a given distance from any void surface. Accordingly, in one embodiment the present invention provides a method of characterising the structure of a void sensitized liquid energetic material, which comprises determining for the material (defining the material in terms of) the fraction of liquid energetic material that occurs at a given distance from any void surface within the void sensitized liquid energetic material. This determination results in a distribution function template for the void-sensitized liquid energetic material. The distribution functions are believed to be new per se and the invention also relates to them as such.
Those skilled in the art of statistical mechanics may see similarities between the distribution function as used in the present invention and the concept of radial distribution function (DF) or pair correlation function that has been applied to describe how the atomic density in a material varies as a function of the distance from a particular atom. One of the uses of the radial distribution function is in providing mathematical relationships that define thermodynamic properties of a material in terms of the positions of atoms in that material.
As will be explained, the bulk detonation energy output for a void-sensitized liquid energetic material can be related to the DF template of the material. Accordingly, in another embodiment the present invention provides a method of achieving a designed bulk detonation energy output in an explosives material comprising sensitizing voids distributed within a liquid energetic material, which method comprises determining a distribution function template that is representative of the designed detonation energy output for the explosives material and formulating an explosive material consistent with that distribution function template by suitable placement and distribution of sensitizing voids within a liquid energetic material. In an embodiment of the invention this may be done by suitable combination of a void-sensitized liquid energetic material with a void-free liquid energetic material. In accordance with the present invention it has been found that structure and detonation properties of the resultant composition is related to the volume ratio of each energetic liquid and the structural arrangement of the energetic liquids relative to each other.
In this embodiment the internal structure of the explosive composition is such that the two energetic materials are present as discrete regions. These regions may be distributed uniformly or randomly throughout the composition. The volume proportion, size and spatial arrangement of the regions define the bulk explosive structure. It has been found that the nature of the energetic liquids used and the bulk structure of the resultant explosive composition influences the energy release characteristics of the explosive composition. Thus, the voids, after their reaction determine amount of shock energy and the regions of void-free liquid energetic material determine the heave energy. Quantitatively, the amount of shock energy is a function of the “total voidage volume” and the amount of heave energy is a function of the void-free component volume fraction.
Importantly, this embodiment allows the energy release characteristics of an explosive composition to be understood and controlled by varying the combination of energetic liquids used and/or the arrangement of the energetic liquids within the bulk of the explosive composition. In turn this enables the detonation properties of the explosive composition to be tailored to particular rock/ground types and to particular mining applications.
While this invention is concerned with the design of liquid explosives, and the detonation performance is determined by the distribution of the voids in the liquid, this does not preclude the addition of small quantities of energetic solids such as aluminium and/or ammonium nitrate prills to further modify the detonation performance.
The present invention also relates to the design of new liquid explosive compositions with novel geometrical distributions of sensitizing voids. A method of mathematically characterizing the internal structure of these explosive compositions is presented. Also an empirical relationship between the internal structure and the bulk detonation properties has been found. A particular advantage of these liquid explosives is the higher energy densities and much higher heave energies that are achievable compared with conventional liquid explosives.
Throughout this specification and the claims which follow, unless the context requires otherwise, the word “comprise”, and variations such as “comprises” and “comprising”, will be understood to imply the inclusion of a stated integer or step or group of integers or steps but not the exclusion of any other integer or step or group of integers or steps.
The reference in this specification to any prior publication (or information derived from it), or to any matter which is known, is not, and should not be taken as an acknowledgment or admission or any form of suggestion that that prior publication (or information derived from it) or known matter forms part of the common general knowledge in the field of endeavour to which this specification relates.
FIGS. 1-19 of PCT/AU2012/001528 are included as part of the present specification and clearly identified as such in the legend to the figure.
As noted above, in the context of the present specification, the distribution function (DF) for a void-sensitized liquid energetic material is a statistical representation of the fraction of liquid energetic material that is within a given distance from any void surface. This can be illustrated with reference to
In
In practice, the randomness of the distribution of the voids will depend on the mixing procedure used, and the corresponding DF may vary from the DF1 template slightly. Nevertheless, it is believed that such changes would not be dramatic: the curve would still be sigmoid in nature and there would be no abrupt changes in the slope of the curve. In relation to such conventional void-sensitized liquid energetic materials the present invention resides in the application of DF to describe/represent the internal structure of the material. The application of statistical modeling involving DF to explosives is unique in this regard.
The present invention is also concerned however with characterizing the internal structure of explosives materials that are new with respect to how voids are distributed within a liquid energetic material, and to the corresponding DF templates associated with such new explosives materials. Noting the random manner in which voids are present in conventional void-sensitized explosive materials, in general terms this new internal structure may be described as involving a non-random (or designed) distribution of voids. In view of this fundamental difference in void distribution, these new explosive materials will have different DF templates when compared with the DF templates associated with conventional materials.
This embodiment of the present invention may be illustrated with reference to unique forms of explosive formulation that have a non-random distribution of voids in a liquid energetic material. Specifically, this explosive is manufactured by blending a void-free energetic liquid with conventional void sensitized energetic liquid. These formulations are referred to as mixtures of emulsion, designated MoE. Careful blending is undertaken to ensure that the finished formulation includes discrete regions of the individual component liquid energetic materials. The explosive can be conveniently prepared by laminar mixing of streams of the individual components using a static mixer (see for example
In relation to
It will be noted that the formulations in which the voids are provided with a non-random (designed) distribution give rise to DFs that have increasingly different shapes from those for conventional emulsions, i.e. DF0 and DF1. For formulations having a non-random void distribution, the plot of DF against radial distance (r) departs from that of conventional formulations with this departure becoming more exaggerated as the dimensions of the void-free emulsion increases.
For DF2, DF3, DF4 and DF6 the exact shape of the curve will vary depending on such factors as the voidage level of the sensitized emulsion and the void distribution of that emulsion.
An alternative method of displaying the differences between DFs for the conventional and non-random void sensitized formulations is to plot the differential of the DF with respect to the distance from the nearest void surface “r”, against the “DF”. This produces a graph that is similar in form to the conventional way of displaying reaction kinetics in the modelling of detonation. In this the reaction rate is plotted against the fraction of material reacted.
Such a DF rate plot is shown in
In relation to
Various aspects are worthy of comment:
Experimental measurements of the distribution functions (DFs) of conventional emulsions (random distribution of voids) were carried out using an X-ray tomography method to record the positions and sizes of voids in a 10 mm×10 mm×1 mm sample of a gassed emulsion. The two dimensional digital record of this was analyzed using commercial image analysis software that identified the outer edges of all the voids, and provided a digital output of the coordinates of the centre and length of the circumference of each void. This data was then used to generate templates for the “DF rate” plots. An X-ray tomography image and analysis of a conventional gas-void emulsion is shown in
The data from this two dimensional analysis was also used to generate “DF rate” graphs. This was done by calculating the distance of each pixel of the digital image that corresponds to emulsion, from the nearest void surface, a computationally intensive operation. The resultant graph of the experimental DF is shown in
It will be noted that DFex and DFsim in
From the foregoing it should be apparent how to generate DF profile templates for void sensitized formulations. The approach may be especially useful for generating DF templates for non-conventional formulations that are typically prepared by blending a conventional void sensitized emulsion with a void-free (or differently sensitized) continuum of liquid energetic material.
The conventional charges were samples of AN-based emulsion explosives prepared by a conventional methodology at densities equal to 1.22 and 1.02 g/cm3 for EM 100 both exhibiting a random distribution of sensitizing voids. The total sensitizing voids volume was equal to about 5.3% for EM 100 at 1.22 g/cm3 and 23% for EM 100 of the AN-based liquid energetic material continuum. The latter was the same for both formulations. With regard to VOD data the solid lines in
The main point to note from this experiment is that the emulsion prepared by a conventional method as per DFsim/DFex templates exhibits an approximately straight line relationship of VOD/idealVOD against inverse diameter. The DF rate profiles for these conventional formulations are reasonably matched to be in line with the DFsim/DFex template in
A non-conventional emulsion explosive formulation (denoted MOE 25) was prepared according to a selected DF rate design template produced in accordance with the present invention. The non-conventional formulation was a blend of 25% mass void sensitized liquid energetic material (density 1.02 g/cc) and 75% mass void-free liquid energetic material continuum (density 1.32 g/cc). The liquid energetic material used was the same as used in formulating the conventional EM 100 control samples. The resulting explosive charges of MOE 25 had a density of 1.23 g/cc.
Experimental samples were prepared in a specially designed emulsion experimental rig shown in
Notably, the relationship between VOD against inverse diameter for this non-conventional formulation was very different from that of the conventional control sample. Indeed, considering that the liquid energetic material continuum used is identical, it is remarkable to see the vast difference between the VOD characteristics for these formulations.
More importantly, the non-conventional formulation shows a characteristic highly concave variation of unconfined normalised detonation velocity (VOD/idealVOD) versus inverse diameter. In contrast, the formulations prepared by conventional methodology exhibit an approximately straight or slightly concave shape from the critical diameter to the ideal VOD.
It is well known to those skilled in the art that at a given explosive density, the shock energy increases with increasing VOD, and that a reduction in VOD corresponds to an increase in heave energy.
For a given liquid energetic material, it is important to note that lower VODs can be obtained in conventional formulations by reducing density, i.e. by increasing the level of voidage include in the liquid energetic material. However, an undesirable effect of this is reduced energy density output and thus lower heave and shock energy.
In distinct contrast, the formulation provided in the present invention enables reduced VOD to be achieved without reducing overall energy density. Thus, such non-conventional formulations may provide a remarkable enhancement in energy density as well as enhanced and unique partitioning of heave energy to shock energy.
In practice implementation of the design aspect of the present invention is likely to involve the following sequence of steps, given by way of illustration with reference to a particular example:
Embodiments of the present invention are illustrated with reference to the following non-limiting examples.
Experimental samples were prepared in a specially designed emulsion experimental rig.
The corresponding process diagram is shown in
The inter-changeable mixing head is comprised of two parts. The first part has two separate inlet channels for the entry of each emulsion stream and a baffle just before the entrance to the first static mixer element to ensure separation of the individual streams in the mixing section. The inter-changeable mixing head is 50 mm diameter and length of 228 mm.
A Kenics static mixer (having 3 elements; see
The density change of the gassing emulsion was determined in a plastic cup of known mass and volume. The emulsion was initially filled to the top of the cup and leveled off. As the gassing reaction progressed, the emulsion rose out of the top of the cup and was leveled off periodically and weighed. The density was determined by dividing the mass of emulsion in the cup by the cup volume. Charges larger than 70 mm in diameter were initiated with a single 400 g Pentex PPP booster, whist smaller charges were initiated with a 150 g Pentex H booster. Velocity of detonation (VOD) was determined using an MREL Handitrap VOD recorder.
Product samples were delivered from the pump rig described above into a 100 mm diameter cylindrical plastic container consisting of a 150 mm tall base, a 10 mm sample slice and a 30 mm tall top slice, as shown in
The photograph of the product structure was analysed using the ImageJ program. A rectangular section of the image was selected for distribution function analysis.
The distribution function (DF) plots the fraction of emulsion that is within a given distance of a void surface. The DF procedure involved calculating the distance from each emulsion pixel to the nearest bubble surface. This program calculated the distance between a pixel and all of the bubble surfaces and returned the distance to the nearest bubble surface. The procedure was then repeated for all emulsion pixels. The frequency of emulsion points residing within a given distance to a bubble surface was then determined and plotted as a cumulative distribution. The differential of the cumulative fraction with respect to distance was also plotted against the cumulative fraction (also referred to as distribution function rate).
This example demonstrates the performance of conventional gassed emulsion with random void distribution at a density of 1.22 g/cm3.
The starting emulsion at a density of 1.32 g/cm3 was delivered by a progressive cavity pump at a rate of 3 kg/min. A 4% mass sodium nitrite solution was injected into the flowing emulsion stream at a rate of 16 g/min by means of a gasser (gear) pump and dispersed in a series of static mixers. 1 m long cardboard tubes with internal diameters ranging from 40 to 180 mm were loaded with emulsion and allowed to gas. Charges were fired once the sample cup reached the target density of 1.22 g/cm3.
A sample of the emulsion was taken for DF analysis according to the procedure described above.
The VOD ranged from 2.9 km/s for the 70 mm diameter charge to 4.3 km/s at 180 mm. Charges smaller than 70 mm failed to sustain detonation. The VOD results are illustrated in
This example demonstrates the performance of MOE25, i.e. a mixture of emulsion with 25% mass sensitized and 75% unsensitized emulsion and was prepared using the apparatus described above.
The base emulsion (density 1.32 g/cm3) was delivered by two progressive cavity pumps, PC1 and PC2. The base emulsion formulation was identical to Example 1 and was the same for both pumps. PC1 pumped ungassed emulsion at a flow rate of 4 kg/min. PC2 delivered emulsion at 1.3 kg/min with gasser (4% NaNO2 solution) injected by a gasser (gear) pump. The emulsion was blended by a static mixer consisting of three helical mixing elements and loaded into cardboard tubes with internal diameters ranging from 70 to 180 mm. The gassed emulsion target density was 0.99 g/cm3 providing an overall density of 1.22 g/cm3 for the mixture of gassed and ungassed emulsion.
A sample of the emulsion was taken for DF analysis according to the procedure described above. The void positions in this sample are shown in
These changes in the distribution function and differential distribution function are reflected in the VOD measurements, shown in
This example demonstrates the performance of MOE50, i.e. a mixture of emulsion with 50% mass gassed and 50% ungassed emulsion.
MOE 50 was prepared using the apparatus mentioned in Example 2. The base emulsion (density 1.32 g/cm3) was delivered by two progressive cavity pumps, PC1 and PC2 and was identical to the previous two examples. PC1 pumped ungassed emulsion at a flow rate of 3 kg/min. PC2 delivered emulsion at 3 kg/min with gasser (4% NaNO2 solution) injected by a gasser (gear) pump. The emulsion was blended by a static mixer consisting of three helical mixing elements and loaded into cardboard tubes with internal diameters ranging from 70 to 180 mm. The gassed emulsion target density was 1.13 g/cm3 providing an overall density of 1.22 g/cm3 for the mixture of gassed and ungassed emulsion.
A sample of the emulsion was taken for DF analysis according to the procedure described above. The void positions in this sample are shown in
The VOD ranged from 2.8 km/s for the 80 mm charge to 3.9 km/s at 180 mm and is illustrated in
The DF of an emulsion with a perfectly random distribution of voids, and that of two idealized (simulated) MoEs with the sensitized and unsensitized regions arranged as alternating flat sheets in which no voids have strayed into the unsensitized region, is shown in
Noting the results obtained in the examples, the present invention also provides explosive compositions comprising sensitizing voids distributed in a liquid energetic materials that are believed to be new per se and that exhibit a characteristic distribution function that is different from known void-sensitized explosive formulations, such as emulsions, watergels and slurry formulations. More specifically, for the explosive compositions of the inventions a plot of distribution function rate versus distribution function includes a point of inflexion, and possibly a concave portion. In contrast corresponding plots for conventional explosive formulations exhibit a characteristic domed profile. As explained above, in this context the “distribution function” (or “distance from void” function) is defined as “the fraction of the liquid that is within a given distance from any void surface”, and the “distribution function rate” is defined as the differential of the “distribution function” with respect to the distance from any void surface.
In an embodiment, for the explosive compositions a plot of distribution function rate versus distribution function comprises a region extending from a distribution function value of 0% to between 10% and 90%, and wherein after the dome region the “distribution function rate” is between 1% and 50% of the peak of the dome. Preferably, the dome region extends from a “distribution function” value of 0% to between 15% and 85%, and in the region after the dome the “distribution function rate” is between 1.5% and 35% of the peak of the dome. Even more preferably the dome region extends from a “distribution function” value of 0% to between 20% and 80%, and in the region after the dome the “distribution function rate” is between 2% and 20% of the peak of the dome.
| Number | Date | Country | Kind |
|---|---|---|---|
| 2013048368 | Jun 2013 | SG | national |
| Filing Document | Filing Date | Country | Kind |
|---|---|---|---|
| PCT/AU2014/050086 | 6/20/2014 | WO | 00 |
