CA1057504A - Conductor containing explosive gas mixture for initiation of ignition element and explosive charge - Google Patents
Conductor containing explosive gas mixture for initiation of ignition element and explosive chargeInfo
- Publication number
- CA1057504A CA1057504A CA242,221A CA242221A CA1057504A CA 1057504 A CA1057504 A CA 1057504A CA 242221 A CA242221 A CA 242221A CA 1057504 A CA1057504 A CA 1057504A
- Authority
- CA
- Canada
- Prior art keywords
- tubular fuse
- gas
- explosive
- detonation
- tubular
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired
Links
- 239000002360 explosive Substances 0.000 title claims abstract description 56
- 239000004020 conductor Substances 0.000 title claims abstract description 17
- 230000000977 initiatory effect Effects 0.000 title claims abstract description 17
- 239000000203 mixture Substances 0.000 title claims description 45
- 239000007789 gas Substances 0.000 claims description 67
- 238000005474 detonation Methods 0.000 claims description 56
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 22
- 239000001301 oxygen Substances 0.000 claims description 22
- 229910052760 oxygen Inorganic materials 0.000 claims description 22
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 21
- 239000000843 powder Substances 0.000 claims description 13
- 239000001257 hydrogen Substances 0.000 claims description 11
- 229910052739 hydrogen Inorganic materials 0.000 claims description 11
- HSFWRNGVRCDJHI-UHFFFAOYSA-N alpha-acetylene Natural products C#C HSFWRNGVRCDJHI-UHFFFAOYSA-N 0.000 claims description 7
- 125000002534 ethynyl group Chemical group [H]C#C* 0.000 claims description 5
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 claims description 5
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 3
- UGFAIRIUMAVXCW-UHFFFAOYSA-N Carbon monoxide Chemical compound [O+]#[C-] UGFAIRIUMAVXCW-UHFFFAOYSA-N 0.000 claims description 2
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 claims description 2
- 229910002091 carbon monoxide Inorganic materials 0.000 claims description 2
- UZGLIIJVICEWHF-UHFFFAOYSA-N octogen Chemical compound [O-][N+](=O)N1CN([N+]([O-])=O)CN([N+]([O-])=O)CN([N+]([O-])=O)C1 UZGLIIJVICEWHF-UHFFFAOYSA-N 0.000 claims description 2
- 239000011248 coating agent Substances 0.000 claims 2
- 238000000576 coating method Methods 0.000 claims 2
- 230000005540 biological transmission Effects 0.000 abstract description 10
- 239000000126 substance Substances 0.000 abstract description 7
- 239000007787 solid Substances 0.000 abstract description 5
- 230000001105 regulatory effect Effects 0.000 abstract description 2
- 230000035939 shock Effects 0.000 description 16
- 238000006243 chemical reaction Methods 0.000 description 12
- 238000002485 combustion reaction Methods 0.000 description 11
- 238000005422 blasting Methods 0.000 description 8
- 230000000694 effects Effects 0.000 description 8
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 6
- 238000000034 method Methods 0.000 description 5
- 230000008569 process Effects 0.000 description 4
- 230000008901 benefit Effects 0.000 description 3
- 238000003780 insertion Methods 0.000 description 3
- 230000037431 insertion Effects 0.000 description 3
- 239000007788 liquid Substances 0.000 description 3
- HXWLJBVVXXBZCM-UHFFFAOYSA-N 2,3-dihydroxypropyl nitrate Chemical compound OCC(O)CO[N+]([O-])=O HXWLJBVVXXBZCM-UHFFFAOYSA-N 0.000 description 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- OAKJQQAXSVQMHS-UHFFFAOYSA-N Hydrazine Chemical compound NN OAKJQQAXSVQMHS-UHFFFAOYSA-N 0.000 description 2
- 239000000654 additive Substances 0.000 description 2
- 150000001540 azides Chemical class 0.000 description 2
- 230000001419 dependent effect Effects 0.000 description 2
- 229910001873 dinitrogen Inorganic materials 0.000 description 2
- 230000002349 favourable effect Effects 0.000 description 2
- 239000012530 fluid Substances 0.000 description 2
- 230000001737 promoting effect Effects 0.000 description 2
- MRMOZBOQVYRSEM-UHFFFAOYSA-N tetraethyllead Chemical compound CC[Pb](CC)(CC)CC MRMOZBOQVYRSEM-UHFFFAOYSA-N 0.000 description 2
- 239000010409 thin film Substances 0.000 description 2
- 230000007704 transition Effects 0.000 description 2
- 235000006576 Althaea officinalis Nutrition 0.000 description 1
- SNIOPGDIGTZGOP-UHFFFAOYSA-N Nitroglycerin Chemical compound [O-][N+](=O)OCC(O[N+]([O-])=O)CO[N+]([O-])=O SNIOPGDIGTZGOP-UHFFFAOYSA-N 0.000 description 1
- 239000004698 Polyethylene Substances 0.000 description 1
- 239000004411 aluminium Substances 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- 239000003990 capacitor Substances 0.000 description 1
- 230000008859 change Effects 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 238000004880 explosion Methods 0.000 description 1
- 239000011261 inert gas Substances 0.000 description 1
- 229920000554 ionomer Polymers 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 150000002894 organic compounds Chemical class 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- -1 polyethylene Polymers 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 229920000915 polyvinyl chloride Polymers 0.000 description 1
- 239000004800 polyvinyl chloride Substances 0.000 description 1
- 230000009467 reduction Effects 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C06—EXPLOSIVES; MATCHES
- C06C—DETONATING OR PRIMING DEVICES; FUSES; CHEMICAL LIGHTERS; PYROPHORIC COMPOSITIONS
- C06C5/00—Fuses, e.g. fuse cords
- C06C5/06—Fuse igniting means; Fuse connectors
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Air Bags (AREA)
Abstract
ABSTRACT OF THE DISCLOSURE
The invention relates to a conductor for transmission of an initiation to an ignition element. In accordance with the invention, the conductor consists of a plastic tube, filled with explosive gas and made in such a way that turbulence is achieved in the ignition zone for the solid ignition substance.
The velocity with which the initiation is transmitted is regu-lated by a chosen component, by chosen components and their relation to each other, by gas pressure, by temperature, and by the inner diameter of the tube.
The invention relates to a conductor for transmission of an initiation to an ignition element. In accordance with the invention, the conductor consists of a plastic tube, filled with explosive gas and made in such a way that turbulence is achieved in the ignition zone for the solid ignition substance.
The velocity with which the initiation is transmitted is regu-lated by a chosen component, by chosen components and their relation to each other, by gas pressure, by temperature, and by the inner diameter of the tube.
Description
1`057S0~
In all handling of explosives, consideration must be taken to how a detonation is transmitted from one place to an-other. The transmission can take place directly through a co-herent string of explosive or it can take place via a shock wave in the medium surrounding the explosives. These two cases are well known, and investigated. They have contributed towards accidents, but have also been utilized in the practical use of explosives.
The transmission through tubes is difficult to judge.
A closed channel conveys the shock wave and can make a trans-rnission at a long distance possible. If the cross-section area is reduced, the losses are increased, and the transmission can be impeded.
A practical case can serve to illustrate the diffi-culties. Glycerol trinitrate was to be transported from one room to another, through a narrow hose. The glycerol nitrate was desensitized with the aid of a solvent, and such a small inner diameter of the hose was chosen that a detonation could not go through the liquid explosive. However, it proved that the empty hose, because of a thin film of explosive, could transmit the detonation. The detonation wa~ transmitted with a speed of 2000 m/sec. The initiation o~ the thin film of liquid took place via the so-called channel ef~ect, i.e. the shock wave which precedes the detonation wave starts the reaction of the glycerol nitrate. A change from air to nitrogen gas, it proved, did not have any influence on the process. This is natural, as the reaction takes place in an explosive, which is not dependent on the surrounding medium for its supply of energy.
It has been endeavoured to utilize this possibility of transmission via a thin layer of explosive, viz. for the designing of a type of detonating cord, shock tube. A hose is coated on the inside with powder or a high explosive. The shock ~05'7S04 wave passing through the channel starts an exothermic reaction in the powder on the walls. The powder or explosive with which the inner surface of the hose is coated is usually not oxygen balanced, and therefore a conversion can take place between the products formed from the explosive substance and the gas which is present in the channel. However, the detonation, i.e. the transmission, is independent of this chemical reaction, which is proved by the fact that the gas can be replaced by an inert gas which cannot react with the explosive substance or the products arising from this at the reaction in the hose.
The difference, in principle, between a detonating cord, the inner chamber of which is filled with an explosive in powder form without a channel through it and a shock tube, the inside of which is coated with an explosive, keeping a channel open is not very great. In both cases it is a question of a deto-nation consisting of a shock wave supported by a reaction zone.
A single phase string of explosive can hardly have been utilized in a detonating cord. It is difficult to find an appropriate system, as the energy transmission from a shock wave to a homogenious medium, as a fluid, is les9 ~avourable than to a powder with many boundary surfaces. We can leave the solid and fluid explosives and consider the conditions in an explosive gas or a gas mixture. A stoichiometric mixture of hydrogen gas and oxygen in normal condition gave a detonation velocity of 2800 m/sec. At a mol relation of H2/02 = 8 a stable detonation of 3500 m/sec. was measured. The initiation took place by means of a spark from a capacitor. Theoretically and experimentally it is possible to determine how the detonation velocity can be regulated through the choice of reaction sub-stances, composition, the gas pressure, and the inner diameter of the tube. A particularly interesting fact is that it is possible to obtain velocities which are lower, to one half of 1(~5750~
the thermodynamically calculated values. The lower velocities have been obtained by roughing up the inner surface of the tube, or by inserting obstructions, e.g. in the form of a spiral. In contrast to this, the rough surface has an accelerating effect on the movement of a flash in the tube. This increase of the velocity is considerable, and it can be a question of a couple of 10th powers. The velocity of the flash can be increased from a few metres per second to several hundred metres per sec-ond. The rough surface can be of importance at the initiation, and can facilitate the transfer to a detonation.
There is no fundamental difference if the gas filling of the tube consists of a mixture of two gases which react with each other, or of a gaseous chemical compound which in itself is explosive, such as acetylene, or hydrazine.
A transmission via a detonating gas is an effect that has been known for a long time. This process can be heard, for instance, when a Bunsen flame goes back. The detonation in the gas mixture was described by Berthelot & Vielle and Mallard &
Le Chatelier as early as in 1881. The detonation wave attains high velocities, from 1000 to 4000 m/sec. i.e. several times sonic speed, in the normal condition. On the basis of the sit-uation in the normal condition, the detonation velocity in gases is quite independent of temperature and pressure. A higher gas pressure involves an increased density and, accordingly, a higher energy concentration and a higher detonation velocity.
For 2H2+02 the velocity increased 2% when the pressure was increased from 1 atm. to 2. An increase of the temperature reduces the density and, accordingly, gives a reduction of the detonation velocity. For a mixture of C2H4 + 2 2 at 10C a detonation velocity of 2580 m/sec. has been measured. At an increase of the temperature to 100C the velocity was reduced to 2540 m/sec. However, the detonation velocity depends to a great l~)5~SO~
extent on the composition of the gas mixture. Outside of a certain range, the mixtu~e can not be caused to detonate. The lower limit for hydrogen gas and air is at l~/o hydrogen gas.
This mixture can still propagate a combustion wave. The limit for comkustion is at 10% hydrogen gas, The upper limit for capability of detonating is at 60% hydrogen gas, while the upper limit for combustion is at 75% hydrogen gas. If the air is replaced by oxygen, the lower limit for capability of detonating is moved to 15% hydrogen gas and the upper limit to 90% hydrogen gas. Within this range, the detonation velocity increases nearly linearily from 1400 m/sec. at 15% hydrogen gas to 3600 m/sec. at 90% hydrogen gas mixed with oxygen.
It is thus well known that a detonation can be generated in a tube containing an explosive gas mixture and that this detonation can be transmitted through the tube. It is also known that turbulence in the explosive gas mixture promotes the transition from combustion to detonation, and that the detonation velocity can be increased through turbulence promoting measures.
An increase of the diameter of the tube, e.g. through an inser-tion into a container with explosive gas has an impeding effect on the detonation, due to the fact that the shock energy i9 distributed over a larger area, and can have the effect that the detonation dies. Even for explosive gas mixtures certain dif-ficulties will thus arise with a narrow tube with explosive gas for transmission of a detonation. The conditions become much more difficult with solid and liquid explosives, which are usually quite unaffected by a detonating gas mixture. Utilizing a det-onation transmission with explosive gas has been prevented by the necessity of using altogether too sensitive substances as a receiver.
It has proved that these difficulties can be overcome, and that a tube with explosive gas can be made to constitute a ~05750~
safe and reliable detonation transmitter. This is made possible through turbulance in the gas mixture just at the charge which is to be initiated.
In one aæpect the invention comprises a conductor for initiation of an ignition element comprising a tubular member filled with an explosive gas, said tubular member having means formed on at least a portion of an inner surface, for creating turbulence in said explosive gas, the turbulence created by said means aiding in the propagation and continuation 10of a detonation of the ex~osive gas to the ignition element.
In a particular embodiment of the invention the con-ductor is in the form of a tubular fuse for initiation of an ignition element, for example, a detonation cap provided with a solid ignition substance.
~_~ - 5 -~OS750~
The initiation of the gas mixture can take place in many ways, The process commences with a combustion, which under certain conditions is transformed into a detonation. The length of the combustion zone is dependent on the composition of the gas mixture, pressure, temperature, and is longer in a wide tube than in a narrow tube. A strong initiation, e.g. via a strong spark, reduces the distance to the start of the detonation.
An exploder is still more efficient. If the tube is widened, the detonation can again be transformed into a combustion which, if the tube is sufficiently long, can again develop into a detonation. The pre-detonation period can also be influenced by additives, e.g. tetra-ethyl lead, which has an impeding effect on the transition into a detonation. However, small quan-tities of additives usually have little effect on the detonation velocity. An exception to this is CO + 2 where the addition of water vapour has a reaction promoting effect on the setting of the equilibrium. The explosion energy of gas mixtures is utilized in practice in various types of engines. Otherwise, it is endeavoured to avoid explosive gas mixtures. The object of the present invention is to utilize an explosive gas mixture at the initiation of an explosive charge.
A tube or a hose can be filled with an explosive gas mixture, e.g. oxyhydrogen gas. One end of the ho~e or tube can be initiated with an exploder, a fuze head, or a spark. It is also possible to ignite the gas, which after a certain length, develops into a detonation. It has now proved that this det-onation in the gas mixture, in turn, can initiate an exploder, an instantaneous exploder as well as an exploder with a delay device. It is thereby possible to use the tube or hose filled - 5a -~)S7~04 with oxyhydrogen gas as a fuze. Several other gas mixtures can come into question. Methane mixed with oxygen, CH4 + 2 2 gives a detoantion velocity of 2150 m/sec. Carbon monoxide and oxygen, 2CO + 2 has a detonation velocity of 1260 m/sec. With 5% H2O the velocity is increased to 1730 m/sec. Acetylene can be used directly as it is, but can also be mixed with oxygen, as with C2H2 + 2 a detonation velocity of 3000 m/sec. can be attained. The oxygen can be added together with nitrogen gas in air, and the velocities will be somewhat lower, but otherwise the fuze will function in the same way. The advantage of using oxygen is that the upper limit for the detonation is substan-tially higher than when air is used. While hydrogen and oxygen has the range of 15 - 90% hydrogen this is reduced to 18 - 60%
hydrogen for a mixture of hydrogen and air. The fuzes have a comparatively low energy content. It is possible to go par-ticularly far in this direction by using certain organic com-pounds mixed with oxygen or air, for which the lower limit is at a couple of percent of combustible substance. A still lower development of effect is achieved by utilizing combustion in-stead of detonation in the explosive gas. The tube or hose can be closed at both end8. As the inner diameter is small, for practical conditions always less than 10mm and usually less than 5mm, there will be no inconvenient leakage of gases when the hose is handled during a short time. It is possible to work with an open hose. Another possibility is to fill the hose with the explosive gas mixture on the work site directly before use. It is possible to carry out the loading work with a hose which contains only air, This is led to the blasting site, where it can be distributed to various lines by means of connection devices. One hose leads to the exploder down in the drill hole, and another runs from the exploder over to the exploder in the next hole. By filling the system with an explosive gas just ~057504 before the blasting is to take place, the salvo can be initiated with the aid of the explosive mixture from a protected place.
With a detonation velocity of more than 2000 m/sec. the delay in the fuze is insignificant, and interval exploders can be used, in the same way as when electric ignition is used. However, this system has the same disadvantage as the electric system,' inasmuch as there must be two conductors to each exploder. They occupy space in the drill hole and, above all, they involve a risk for incorrect connections. It has now proved to be possible to work with a tube system that has been filled in advance, by the hose with the explosive gas mixture being crimped tightly at the exploders and the connection of the ignition tubes from the different drill holes being made with a small exploder con-taining initiating means, whereby the hose will be closed every-where, The ignition of the gas fuze can appropriately take place by means of an ignition charge which is inserted in the far end of the conductor which transmits the initiation to the blasting site, after which this end is closed gas tight.
The hoses that are inserted into the drill holes are consumed. According to the procedure stated herein, there is only one hose in each drill hole, whereby the cost of ignition hose is reduced, compared with the case when the explosive gas is inserted after the loading. In the same way, it is suf-ficient to have one single conductor to the explosive charge from the protected ignition position. It is an advantage to have the hose leading from the ignition position to the blasting site made with a larger diameter than the hose that is inserted into the drill holes. It corresponds to the ignition cable used for electric ignition and, as in the case of this, can be used a number of times. After a blasting operation, its tightness should be checked, damaged parts removed, and thereafter it should be spliced, if required, and filled with explosive ~057504 gas. Under certain conditions it can be an advantage to ill this conductor corresponding to the ignition cable with explosive gas from the ignition position just before the blasting is to be carried out. A feed conductor and a return conductor can then be used, in order to be able to check that a sufficient quantity of gas has been filled in. It is more simple, and cheaper, to work with a hose which is open in the end that has been laid out to the blasting site, and so much gas being filled in that it will be ensured that it is sufficient to fill the conductor to the first exploder.
The explosive gas fuze is an excellent member for use in combination with shock tubes, as a conductor from the pro-tected ignition position to the blasting site. It is thereby possible to overcome one difficulty with the shock tube, which is too expensive to be used for this purpose, as it cannot be refilled. Electric ignition can be used, but this fails to serve the purpose of the shock fuze, which has an essential pur-pose to fulfill of avoiding risks of unintentional electric ignition. In this respect the fuze with explosive gas fulfills the same severe requirements as a shock tube in a nonelectric conducting material.
The explosive gas mixture can be caused to detonate directly with the aid of a fuze head or through ignition by a sufficiently violent shock wave. The gas can be ignited with a flame, for instance from a match. Depending on the compo-sition of the gas and the inner diameter of the hose, the com-bustion will die, continue at a low speed, or develop into a detonation. The development into a detonation takes place through turbulence in the combustion zone, and this process can therefore be furthered by roughing the walls in the hose by means of rifling or the insertion of a powder. A larger diameter in the vicinity of the ignition point is also favourable, a ~()S7~0~
smaller hose being used for the other parts, to keep the costs down, at the same time as the fuze is made easier to handle.
EXAMPLE 1.
A polyvinyl chloride hose with an inner diameter of 7mm and an outer diameter of lOmm was filled with a stoichio-metric mixture of hydrogen and oxygen, The hose was connected to another one with an inner diameter of 4mm and an outer diam-eter of 7mm, which was filled with the same explosive mixture and the other end of which was inserted in an exploder which was crimped on to the hose. The free end of the larger hose was initiated by means of a fuze head. The detonation was transmitted to the exploder via the conductor. Trials were carried out with instantaneous exploders, the detonation in the gas mixture then igniting lead azide, as well as with exploders with delay devices, the explosive gas mixture then igniting the delay composition which, after the time set, initiated the lead azide in the exploders.
EXAMPLE 2.
An ionomer polymer hose with an inner diameter of 3mm was filled with a mixture of equal parts of acetylene and oxygen.
Initiation took place at one end by means of an exploder. The detonation was conveyed through the hose, down into a drill hole, where an exploder crimped on to the other end was initiated.
EXAMPLE 3.
The larger hose according to example 1 was moistened on the inside with benzene, and after a storage time of 10 min.
the fuze was initiated with a fuze head. After the detonation, the inside of the hose was coated with a very fine-grained carbon powder. The hose was moistened anew on the inside with benzene, after which oxygen was fed through the hose. Initiation was carried out by means of an exploder. A detonation velocity of 3200 m/sec.was measured, and the reaction was clearly stronger _ g _ 105750~
than when air was used instead of oxygen.
When refilled, a hose that has previously been used with a gas mixture which leaves solid particles such as carbon powder is favourable for a development from combustion to det-onation. The insertion of metal powder gives a still better effect. A hose with an inner diameter of 7mm and an outer diameter of lOmm was powdered on the inside with fine-grained aluminium, after which the hose was filled with hydrogen and oxygen in a mol relation of H2/02 = 8. The gas was ignited with a match. The exothermic reaction in the hose started as a combustion, increased in velocity, and developed into a det-onation with a velocity of 3500 m/sec.
A polyethylene hose with an inner diameter of 5mm was filled with a stoichiometric mixture of hydrogen and oxygen, after which one end of it was put on to a shock tube with an inner diameter of 1.5mm. The inside of the shock tube was pow-dered wlth fine-grained tetramethylene tetranitramine. The free end of the gas fuze was ignited with a match. The exothermic reaction in the gas mixture started the detonation in the shoc]c fuze.
In all handling of explosives, consideration must be taken to how a detonation is transmitted from one place to an-other. The transmission can take place directly through a co-herent string of explosive or it can take place via a shock wave in the medium surrounding the explosives. These two cases are well known, and investigated. They have contributed towards accidents, but have also been utilized in the practical use of explosives.
The transmission through tubes is difficult to judge.
A closed channel conveys the shock wave and can make a trans-rnission at a long distance possible. If the cross-section area is reduced, the losses are increased, and the transmission can be impeded.
A practical case can serve to illustrate the diffi-culties. Glycerol trinitrate was to be transported from one room to another, through a narrow hose. The glycerol nitrate was desensitized with the aid of a solvent, and such a small inner diameter of the hose was chosen that a detonation could not go through the liquid explosive. However, it proved that the empty hose, because of a thin film of explosive, could transmit the detonation. The detonation wa~ transmitted with a speed of 2000 m/sec. The initiation o~ the thin film of liquid took place via the so-called channel ef~ect, i.e. the shock wave which precedes the detonation wave starts the reaction of the glycerol nitrate. A change from air to nitrogen gas, it proved, did not have any influence on the process. This is natural, as the reaction takes place in an explosive, which is not dependent on the surrounding medium for its supply of energy.
It has been endeavoured to utilize this possibility of transmission via a thin layer of explosive, viz. for the designing of a type of detonating cord, shock tube. A hose is coated on the inside with powder or a high explosive. The shock ~05'7S04 wave passing through the channel starts an exothermic reaction in the powder on the walls. The powder or explosive with which the inner surface of the hose is coated is usually not oxygen balanced, and therefore a conversion can take place between the products formed from the explosive substance and the gas which is present in the channel. However, the detonation, i.e. the transmission, is independent of this chemical reaction, which is proved by the fact that the gas can be replaced by an inert gas which cannot react with the explosive substance or the products arising from this at the reaction in the hose.
The difference, in principle, between a detonating cord, the inner chamber of which is filled with an explosive in powder form without a channel through it and a shock tube, the inside of which is coated with an explosive, keeping a channel open is not very great. In both cases it is a question of a deto-nation consisting of a shock wave supported by a reaction zone.
A single phase string of explosive can hardly have been utilized in a detonating cord. It is difficult to find an appropriate system, as the energy transmission from a shock wave to a homogenious medium, as a fluid, is les9 ~avourable than to a powder with many boundary surfaces. We can leave the solid and fluid explosives and consider the conditions in an explosive gas or a gas mixture. A stoichiometric mixture of hydrogen gas and oxygen in normal condition gave a detonation velocity of 2800 m/sec. At a mol relation of H2/02 = 8 a stable detonation of 3500 m/sec. was measured. The initiation took place by means of a spark from a capacitor. Theoretically and experimentally it is possible to determine how the detonation velocity can be regulated through the choice of reaction sub-stances, composition, the gas pressure, and the inner diameter of the tube. A particularly interesting fact is that it is possible to obtain velocities which are lower, to one half of 1(~5750~
the thermodynamically calculated values. The lower velocities have been obtained by roughing up the inner surface of the tube, or by inserting obstructions, e.g. in the form of a spiral. In contrast to this, the rough surface has an accelerating effect on the movement of a flash in the tube. This increase of the velocity is considerable, and it can be a question of a couple of 10th powers. The velocity of the flash can be increased from a few metres per second to several hundred metres per sec-ond. The rough surface can be of importance at the initiation, and can facilitate the transfer to a detonation.
There is no fundamental difference if the gas filling of the tube consists of a mixture of two gases which react with each other, or of a gaseous chemical compound which in itself is explosive, such as acetylene, or hydrazine.
A transmission via a detonating gas is an effect that has been known for a long time. This process can be heard, for instance, when a Bunsen flame goes back. The detonation in the gas mixture was described by Berthelot & Vielle and Mallard &
Le Chatelier as early as in 1881. The detonation wave attains high velocities, from 1000 to 4000 m/sec. i.e. several times sonic speed, in the normal condition. On the basis of the sit-uation in the normal condition, the detonation velocity in gases is quite independent of temperature and pressure. A higher gas pressure involves an increased density and, accordingly, a higher energy concentration and a higher detonation velocity.
For 2H2+02 the velocity increased 2% when the pressure was increased from 1 atm. to 2. An increase of the temperature reduces the density and, accordingly, gives a reduction of the detonation velocity. For a mixture of C2H4 + 2 2 at 10C a detonation velocity of 2580 m/sec. has been measured. At an increase of the temperature to 100C the velocity was reduced to 2540 m/sec. However, the detonation velocity depends to a great l~)5~SO~
extent on the composition of the gas mixture. Outside of a certain range, the mixtu~e can not be caused to detonate. The lower limit for hydrogen gas and air is at l~/o hydrogen gas.
This mixture can still propagate a combustion wave. The limit for comkustion is at 10% hydrogen gas, The upper limit for capability of detonating is at 60% hydrogen gas, while the upper limit for combustion is at 75% hydrogen gas. If the air is replaced by oxygen, the lower limit for capability of detonating is moved to 15% hydrogen gas and the upper limit to 90% hydrogen gas. Within this range, the detonation velocity increases nearly linearily from 1400 m/sec. at 15% hydrogen gas to 3600 m/sec. at 90% hydrogen gas mixed with oxygen.
It is thus well known that a detonation can be generated in a tube containing an explosive gas mixture and that this detonation can be transmitted through the tube. It is also known that turbulence in the explosive gas mixture promotes the transition from combustion to detonation, and that the detonation velocity can be increased through turbulence promoting measures.
An increase of the diameter of the tube, e.g. through an inser-tion into a container with explosive gas has an impeding effect on the detonation, due to the fact that the shock energy i9 distributed over a larger area, and can have the effect that the detonation dies. Even for explosive gas mixtures certain dif-ficulties will thus arise with a narrow tube with explosive gas for transmission of a detonation. The conditions become much more difficult with solid and liquid explosives, which are usually quite unaffected by a detonating gas mixture. Utilizing a det-onation transmission with explosive gas has been prevented by the necessity of using altogether too sensitive substances as a receiver.
It has proved that these difficulties can be overcome, and that a tube with explosive gas can be made to constitute a ~05750~
safe and reliable detonation transmitter. This is made possible through turbulance in the gas mixture just at the charge which is to be initiated.
In one aæpect the invention comprises a conductor for initiation of an ignition element comprising a tubular member filled with an explosive gas, said tubular member having means formed on at least a portion of an inner surface, for creating turbulence in said explosive gas, the turbulence created by said means aiding in the propagation and continuation 10of a detonation of the ex~osive gas to the ignition element.
In a particular embodiment of the invention the con-ductor is in the form of a tubular fuse for initiation of an ignition element, for example, a detonation cap provided with a solid ignition substance.
~_~ - 5 -~OS750~
The initiation of the gas mixture can take place in many ways, The process commences with a combustion, which under certain conditions is transformed into a detonation. The length of the combustion zone is dependent on the composition of the gas mixture, pressure, temperature, and is longer in a wide tube than in a narrow tube. A strong initiation, e.g. via a strong spark, reduces the distance to the start of the detonation.
An exploder is still more efficient. If the tube is widened, the detonation can again be transformed into a combustion which, if the tube is sufficiently long, can again develop into a detonation. The pre-detonation period can also be influenced by additives, e.g. tetra-ethyl lead, which has an impeding effect on the transition into a detonation. However, small quan-tities of additives usually have little effect on the detonation velocity. An exception to this is CO + 2 where the addition of water vapour has a reaction promoting effect on the setting of the equilibrium. The explosion energy of gas mixtures is utilized in practice in various types of engines. Otherwise, it is endeavoured to avoid explosive gas mixtures. The object of the present invention is to utilize an explosive gas mixture at the initiation of an explosive charge.
A tube or a hose can be filled with an explosive gas mixture, e.g. oxyhydrogen gas. One end of the ho~e or tube can be initiated with an exploder, a fuze head, or a spark. It is also possible to ignite the gas, which after a certain length, develops into a detonation. It has now proved that this det-onation in the gas mixture, in turn, can initiate an exploder, an instantaneous exploder as well as an exploder with a delay device. It is thereby possible to use the tube or hose filled - 5a -~)S7~04 with oxyhydrogen gas as a fuze. Several other gas mixtures can come into question. Methane mixed with oxygen, CH4 + 2 2 gives a detoantion velocity of 2150 m/sec. Carbon monoxide and oxygen, 2CO + 2 has a detonation velocity of 1260 m/sec. With 5% H2O the velocity is increased to 1730 m/sec. Acetylene can be used directly as it is, but can also be mixed with oxygen, as with C2H2 + 2 a detonation velocity of 3000 m/sec. can be attained. The oxygen can be added together with nitrogen gas in air, and the velocities will be somewhat lower, but otherwise the fuze will function in the same way. The advantage of using oxygen is that the upper limit for the detonation is substan-tially higher than when air is used. While hydrogen and oxygen has the range of 15 - 90% hydrogen this is reduced to 18 - 60%
hydrogen for a mixture of hydrogen and air. The fuzes have a comparatively low energy content. It is possible to go par-ticularly far in this direction by using certain organic com-pounds mixed with oxygen or air, for which the lower limit is at a couple of percent of combustible substance. A still lower development of effect is achieved by utilizing combustion in-stead of detonation in the explosive gas. The tube or hose can be closed at both end8. As the inner diameter is small, for practical conditions always less than 10mm and usually less than 5mm, there will be no inconvenient leakage of gases when the hose is handled during a short time. It is possible to work with an open hose. Another possibility is to fill the hose with the explosive gas mixture on the work site directly before use. It is possible to carry out the loading work with a hose which contains only air, This is led to the blasting site, where it can be distributed to various lines by means of connection devices. One hose leads to the exploder down in the drill hole, and another runs from the exploder over to the exploder in the next hole. By filling the system with an explosive gas just ~057504 before the blasting is to take place, the salvo can be initiated with the aid of the explosive mixture from a protected place.
With a detonation velocity of more than 2000 m/sec. the delay in the fuze is insignificant, and interval exploders can be used, in the same way as when electric ignition is used. However, this system has the same disadvantage as the electric system,' inasmuch as there must be two conductors to each exploder. They occupy space in the drill hole and, above all, they involve a risk for incorrect connections. It has now proved to be possible to work with a tube system that has been filled in advance, by the hose with the explosive gas mixture being crimped tightly at the exploders and the connection of the ignition tubes from the different drill holes being made with a small exploder con-taining initiating means, whereby the hose will be closed every-where, The ignition of the gas fuze can appropriately take place by means of an ignition charge which is inserted in the far end of the conductor which transmits the initiation to the blasting site, after which this end is closed gas tight.
The hoses that are inserted into the drill holes are consumed. According to the procedure stated herein, there is only one hose in each drill hole, whereby the cost of ignition hose is reduced, compared with the case when the explosive gas is inserted after the loading. In the same way, it is suf-ficient to have one single conductor to the explosive charge from the protected ignition position. It is an advantage to have the hose leading from the ignition position to the blasting site made with a larger diameter than the hose that is inserted into the drill holes. It corresponds to the ignition cable used for electric ignition and, as in the case of this, can be used a number of times. After a blasting operation, its tightness should be checked, damaged parts removed, and thereafter it should be spliced, if required, and filled with explosive ~057504 gas. Under certain conditions it can be an advantage to ill this conductor corresponding to the ignition cable with explosive gas from the ignition position just before the blasting is to be carried out. A feed conductor and a return conductor can then be used, in order to be able to check that a sufficient quantity of gas has been filled in. It is more simple, and cheaper, to work with a hose which is open in the end that has been laid out to the blasting site, and so much gas being filled in that it will be ensured that it is sufficient to fill the conductor to the first exploder.
The explosive gas fuze is an excellent member for use in combination with shock tubes, as a conductor from the pro-tected ignition position to the blasting site. It is thereby possible to overcome one difficulty with the shock tube, which is too expensive to be used for this purpose, as it cannot be refilled. Electric ignition can be used, but this fails to serve the purpose of the shock fuze, which has an essential pur-pose to fulfill of avoiding risks of unintentional electric ignition. In this respect the fuze with explosive gas fulfills the same severe requirements as a shock tube in a nonelectric conducting material.
The explosive gas mixture can be caused to detonate directly with the aid of a fuze head or through ignition by a sufficiently violent shock wave. The gas can be ignited with a flame, for instance from a match. Depending on the compo-sition of the gas and the inner diameter of the hose, the com-bustion will die, continue at a low speed, or develop into a detonation. The development into a detonation takes place through turbulence in the combustion zone, and this process can therefore be furthered by roughing the walls in the hose by means of rifling or the insertion of a powder. A larger diameter in the vicinity of the ignition point is also favourable, a ~()S7~0~
smaller hose being used for the other parts, to keep the costs down, at the same time as the fuze is made easier to handle.
EXAMPLE 1.
A polyvinyl chloride hose with an inner diameter of 7mm and an outer diameter of lOmm was filled with a stoichio-metric mixture of hydrogen and oxygen, The hose was connected to another one with an inner diameter of 4mm and an outer diam-eter of 7mm, which was filled with the same explosive mixture and the other end of which was inserted in an exploder which was crimped on to the hose. The free end of the larger hose was initiated by means of a fuze head. The detonation was transmitted to the exploder via the conductor. Trials were carried out with instantaneous exploders, the detonation in the gas mixture then igniting lead azide, as well as with exploders with delay devices, the explosive gas mixture then igniting the delay composition which, after the time set, initiated the lead azide in the exploders.
EXAMPLE 2.
An ionomer polymer hose with an inner diameter of 3mm was filled with a mixture of equal parts of acetylene and oxygen.
Initiation took place at one end by means of an exploder. The detonation was conveyed through the hose, down into a drill hole, where an exploder crimped on to the other end was initiated.
EXAMPLE 3.
The larger hose according to example 1 was moistened on the inside with benzene, and after a storage time of 10 min.
the fuze was initiated with a fuze head. After the detonation, the inside of the hose was coated with a very fine-grained carbon powder. The hose was moistened anew on the inside with benzene, after which oxygen was fed through the hose. Initiation was carried out by means of an exploder. A detonation velocity of 3200 m/sec.was measured, and the reaction was clearly stronger _ g _ 105750~
than when air was used instead of oxygen.
When refilled, a hose that has previously been used with a gas mixture which leaves solid particles such as carbon powder is favourable for a development from combustion to det-onation. The insertion of metal powder gives a still better effect. A hose with an inner diameter of 7mm and an outer diameter of lOmm was powdered on the inside with fine-grained aluminium, after which the hose was filled with hydrogen and oxygen in a mol relation of H2/02 = 8. The gas was ignited with a match. The exothermic reaction in the hose started as a combustion, increased in velocity, and developed into a det-onation with a velocity of 3500 m/sec.
A polyethylene hose with an inner diameter of 5mm was filled with a stoichiometric mixture of hydrogen and oxygen, after which one end of it was put on to a shock tube with an inner diameter of 1.5mm. The inside of the shock tube was pow-dered wlth fine-grained tetramethylene tetranitramine. The free end of the gas fuze was ignited with a match. The exothermic reaction in the gas mixture started the detonation in the shoc]c fuze.
Claims (14)
1. In a tubular fuse for initiation of an ignition element, said tubular fuse being filled with an explosive gas, the improvement which comprises: means formed on at least a portion of the inner surface of said tubular fuse for creating turbulence of said explosive gas, the turbulence created by said means aiding in the propogation and continuation of a detonation of the explosive gas to the ignition element.
2. The tubular fuse according to claim 1, wherein said inner surface is a circumferential surface.
3. The tubular fuse according to claim 1, wherein said means for creating turbulence comprises a powder coating said inner surface of said tubular fuse.
4. The tubular fuse according to claim 2, wherein said means for creating turbulence comprises a powder coating said inner surface of said tubular fuse.
5. The tubular fuse according to claim 3 or 4, wherein said powder is a fine-grained carbon powder.
6. The tubular fuse according to claim 3 or 4, wherein said powder is a fine-grained aluminum powder.
7. The tubular fuse according to claim 3 or 4, wherein said powder is a fine-grained tetramethylene tetranitramine powder.
8. The tubular fuse according to claim 1 or 2, wherein said inner surface comprises a roughened surface, said roughened surface constituting aid means for creating turbulence.
9. The tubular fuse according to claim 1 or 2, wherein said means for creating turbulence of said explosive gas extends the whole length of said tubular fuse.
10. The tubular fuse of claim 1 or 2, wherein said tubular fuse is of plastic.
11. The tubular fuse of claim 1 or 2, wherein the gas is selected from a mixture of oxygen and hydrogen; acetylene;
a mixture of acetylene and oxygen; a mixture of air and hydrogen; a mixture of methane and oxygen; and a mixture of carbon monoxide and oxygen.
a mixture of acetylene and oxygen; a mixture of air and hydrogen; a mixture of methane and oxygen; and a mixture of carbon monoxide and oxygen.
12. The tubular fuse of claim 1 or 2, wherein the gas consists of a mixture of hydrogen and oxygen, having a hydrogen content of 15 to 90 percent by weight.
13. A conductor for initiation of an ignition element comprising a tubular member filled with an explosive gas, said tubular member having means formed on at least a portion of an inner surface, for creating turbulence in said explosive gas, the turbulence created by said means aiding in the propagation and continuation of a detonation of the explosive gas to the ignition element.
14. A conductor according to claim 13, wherein said tubular member is of plastic.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| SE7416111A SE7416111L (en) | 1974-12-20 | 1974-12-20 | LEADER HOLDING EXPLOSIVE GAS MIXTURE FOR INITIATION OF IGNITION ELEMENTS AND EXPLOSIVE CHARGE. |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CA1057504A true CA1057504A (en) | 1979-07-03 |
Family
ID=20323081
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CA242,221A Expired CA1057504A (en) | 1974-12-20 | 1975-12-18 | Conductor containing explosive gas mixture for initiation of ignition element and explosive charge |
Country Status (5)
| Country | Link |
|---|---|
| JP (1) | JPS5188619A (en) |
| CA (1) | CA1057504A (en) |
| GB (1) | GB1527620A (en) |
| SE (1) | SE7416111L (en) |
| ZA (1) | ZA757889B (en) |
Families Citing this family (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| BR8400206A (en) * | 1984-01-13 | 1984-09-11 | Britanite Ind Quimicas Ltd | PERCUSION WAVE CONDUCTING UNIT OR IMPACT |
| RU2151758C1 (en) * | 1998-09-03 | 2000-06-27 | Товарищество с ограниченной ответственностью "Научно-производственный центр "Квазар-ВВ" | Detonating cord and method for manufacture of detonating cord |
| CN108535446B (en) * | 2018-04-19 | 2023-08-22 | 河南工程学院 | Experimental device and method for secondary explosion of deposited coal dust caused by gas explosion of pipeline |
-
1974
- 1974-12-20 SE SE7416111A patent/SE7416111L/en unknown
-
1975
- 1975-12-15 GB GB51212/75A patent/GB1527620A/en not_active Expired
- 1975-12-18 CA CA242,221A patent/CA1057504A/en not_active Expired
- 1975-12-19 JP JP50152680A patent/JPS5188619A/ja active Pending
- 1975-12-19 ZA ZA757889A patent/ZA757889B/en unknown
Also Published As
| Publication number | Publication date |
|---|---|
| ZA757889B (en) | 1977-07-27 |
| GB1527620A (en) | 1978-10-04 |
| JPS5188619A (en) | 1976-08-03 |
| SE7416111L (en) | 1976-06-21 |
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