EP0000523A1 - Cordeau et procédé de fabrication - Google Patents
Cordeau et procédé de fabrication Download PDFInfo
- Publication number
- EP0000523A1 EP0000523A1 EP78100402A EP78100402A EP0000523A1 EP 0000523 A1 EP0000523 A1 EP 0000523A1 EP 78100402 A EP78100402 A EP 78100402A EP 78100402 A EP78100402 A EP 78100402A EP 0000523 A1 EP0000523 A1 EP 0000523A1
- Authority
- EP
- European Patent Office
- Prior art keywords
- fusecord
- improved
- sheath
- strands
- adhesive
- 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.)
- Granted
Links
- 238000000034 method Methods 0.000 title claims description 22
- 230000008569 process Effects 0.000 title claims description 16
- 239000000853 adhesive Substances 0.000 claims abstract description 77
- 230000001070 adhesive effect Effects 0.000 claims abstract description 77
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- 229920001169 thermoplastic Polymers 0.000 claims abstract description 24
- 239000004416 thermosoftening plastic Substances 0.000 claims abstract description 24
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 16
- 239000000306 component Substances 0.000 claims description 39
- 239000000463 material Substances 0.000 claims description 28
- -1 poly(vinyl alcohol) Polymers 0.000 claims description 26
- 239000002360 explosive Substances 0.000 claims description 14
- 229920001577 copolymer Polymers 0.000 claims description 12
- 239000007788 liquid Substances 0.000 claims description 9
- TZRXHJWUDPFEEY-UHFFFAOYSA-N Pentaerythritol Tetranitrate Chemical compound [O-][N+](=O)OCC(CO[N+]([O-])=O)(CO[N+]([O-])=O)CO[N+]([O-])=O TZRXHJWUDPFEEY-UHFFFAOYSA-N 0.000 claims description 6
- 239000000026 Pentaerythritol tetranitrate Substances 0.000 claims description 6
- 239000008358 core component Substances 0.000 claims description 6
- 230000006872 improvement Effects 0.000 claims description 6
- 229960004321 pentaerithrityl tetranitrate Drugs 0.000 claims description 6
- IJFPVINAQGWBRJ-UHFFFAOYSA-N Diisooctyl phthalate Chemical group CC(C)CCCCCOC(=O)C1=CC=CC=C1C(=O)OCCCCCC(C)C IJFPVINAQGWBRJ-UHFFFAOYSA-N 0.000 claims description 5
- 238000005422 blasting Methods 0.000 claims description 5
- 229920000728 polyester Polymers 0.000 claims description 5
- 229920002689 polyvinyl acetate Polymers 0.000 claims description 5
- 239000011118 polyvinyl acetate Substances 0.000 claims description 5
- 238000009987 spinning Methods 0.000 claims description 5
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 claims description 4
- 239000005977 Ethylene Substances 0.000 claims description 4
- 229920012485 Plasticized Polyvinyl chloride Polymers 0.000 claims description 4
- 238000001035 drying Methods 0.000 claims description 4
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- 239000000843 powder Substances 0.000 claims description 4
- 239000005060 rubber Substances 0.000 claims description 4
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 claims description 3
- 230000005540 biological transmission Effects 0.000 claims description 3
- 238000005474 detonation Methods 0.000 claims description 3
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- OFOBLEOULBTSOW-UHFFFAOYSA-N Malonic acid Chemical compound OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 claims description 2
- 125000003118 aryl group Chemical group 0.000 claims description 2
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- LNEPOXFFQSENCJ-UHFFFAOYSA-N haloperidol Chemical compound C1CC(O)(C=2C=CC(Cl)=CC=2)CCN1CCCC(=O)C1=CC=C(F)C=C1 LNEPOXFFQSENCJ-UHFFFAOYSA-N 0.000 claims description 2
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- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 claims description 2
- 229920002554 vinyl polymer Polymers 0.000 claims description 2
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 claims 1
- 229920006163 vinyl copolymer Polymers 0.000 claims 1
- 229920000139 polyethylene terephthalate Polymers 0.000 description 7
- 239000005020 polyethylene terephthalate Substances 0.000 description 7
- 239000004698 Polyethylene Substances 0.000 description 6
- 229920000573 polyethylene Polymers 0.000 description 6
- 230000000694 effects Effects 0.000 description 5
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- 239000004743 Polypropylene Substances 0.000 description 4
- 150000001875 compounds Chemical class 0.000 description 4
- 229920003023 plastic Polymers 0.000 description 4
- 239000004033 plastic Substances 0.000 description 4
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- 240000000491 Corchorus aestuans Species 0.000 description 3
- 235000011777 Corchorus aestuans Nutrition 0.000 description 3
- 235000010862 Corchorus capsularis Nutrition 0.000 description 3
- 229920000742 Cotton Polymers 0.000 description 3
- 239000000295 fuel oil Substances 0.000 description 3
- 239000012943 hotmelt Substances 0.000 description 3
- 238000005065 mining Methods 0.000 description 3
- 230000004048 modification Effects 0.000 description 3
- 238000012986 modification Methods 0.000 description 3
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- 238000003860 storage Methods 0.000 description 3
- 239000004753 textile Substances 0.000 description 3
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
- 229920000297 Rayon Polymers 0.000 description 2
- 230000009471 action Effects 0.000 description 2
- 239000000654 additive Substances 0.000 description 2
- 239000011248 coating agent Substances 0.000 description 2
- 238000000576 coating method Methods 0.000 description 2
- 239000000470 constituent Substances 0.000 description 2
- 239000011521 glass Substances 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 239000000123 paper Substances 0.000 description 2
- 229920000642 polymer Polymers 0.000 description 2
- 229920002635 polyurethane Polymers 0.000 description 2
- 239000004814 polyurethane Substances 0.000 description 2
- 229920000915 polyvinyl chloride Polymers 0.000 description 2
- 239000004800 polyvinyl chloride Substances 0.000 description 2
- FGIUAXJPYTZDNR-UHFFFAOYSA-N potassium nitrate Chemical compound [K+].[O-][N+]([O-])=O FGIUAXJPYTZDNR-UHFFFAOYSA-N 0.000 description 2
- 230000005855 radiation Effects 0.000 description 2
- 239000002964 rayon Substances 0.000 description 2
- 239000007787 solid Substances 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- XTFIVUDBNACUBN-UHFFFAOYSA-N 1,3,5-trinitro-1,3,5-triazinane Chemical compound [O-][N+](=O)N1CN([N+]([O-])=O)CN([N+]([O-])=O)C1 XTFIVUDBNACUBN-UHFFFAOYSA-N 0.000 description 1
- PAWQVTBBRAZDMG-UHFFFAOYSA-N 2-(3-bromo-2-fluorophenyl)acetic acid Chemical compound OC(=O)CC1=CC=CC(Br)=C1F PAWQVTBBRAZDMG-UHFFFAOYSA-N 0.000 description 1
- SIXWIUJQBBANGK-UHFFFAOYSA-N 4-(4-fluorophenyl)-1h-pyrazol-5-amine Chemical compound N1N=CC(C=2C=CC(F)=CC=2)=C1N SIXWIUJQBBANGK-UHFFFAOYSA-N 0.000 description 1
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 1
- 241000196324 Embryophyta Species 0.000 description 1
- JIGUQPWFLRLWPJ-UHFFFAOYSA-N Ethyl acrylate Chemical compound CCOC(=O)C=C JIGUQPWFLRLWPJ-UHFFFAOYSA-N 0.000 description 1
- 244000043261 Hevea brasiliensis Species 0.000 description 1
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
- VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 description 1
- 239000004952 Polyamide Substances 0.000 description 1
- 239000004372 Polyvinyl alcohol Substances 0.000 description 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 1
- 239000005864 Sulphur Substances 0.000 description 1
- 244000223014 Syzygium aromaticum Species 0.000 description 1
- 235000016639 Syzygium aromaticum Nutrition 0.000 description 1
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 description 1
- 239000003929 acidic solution Substances 0.000 description 1
- 238000007605 air drying Methods 0.000 description 1
- 150000001336 alkenes Chemical class 0.000 description 1
- 125000005250 alkyl acrylate group Chemical group 0.000 description 1
- 230000008901 benefit Effects 0.000 description 1
- 239000007767 bonding agent Substances 0.000 description 1
- 238000009954 braiding Methods 0.000 description 1
- CQEYYJKEWSMYFG-UHFFFAOYSA-N butyl acrylate Chemical compound CCCCOC(=O)C=C CQEYYJKEWSMYFG-UHFFFAOYSA-N 0.000 description 1
- 239000003575 carbonaceous material Substances 0.000 description 1
- 230000015556 catabolic process Effects 0.000 description 1
- 230000001413 cellular effect Effects 0.000 description 1
- 210000003850 cellular structure Anatomy 0.000 description 1
- 229920002678 cellulose Polymers 0.000 description 1
- 239000001913 cellulose Substances 0.000 description 1
- 229920002301 cellulose acetate Polymers 0.000 description 1
- 239000003610 charcoal Substances 0.000 description 1
- 238000010276 construction Methods 0.000 description 1
- 238000006731 degradation reaction Methods 0.000 description 1
- 230000001419 dependent effect Effects 0.000 description 1
- 238000001125 extrusion Methods 0.000 description 1
- 239000006260 foam Substances 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 238000007689 inspection Methods 0.000 description 1
- 229920003052 natural elastomer Polymers 0.000 description 1
- 229930014626 natural product Natural products 0.000 description 1
- 229920001194 natural rubber Polymers 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- PNJWIWWMYCMZRO-UHFFFAOYSA-N pent‐4‐en‐2‐one Natural products CC(=O)CC=C PNJWIWWMYCMZRO-UHFFFAOYSA-N 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 239000004014 plasticizer Substances 0.000 description 1
- 229920000058 polyacrylate Polymers 0.000 description 1
- 229920002647 polyamide Polymers 0.000 description 1
- 229920000098 polyolefin Polymers 0.000 description 1
- 235000010333 potassium nitrate Nutrition 0.000 description 1
- 239000004323 potassium nitrate Substances 0.000 description 1
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 1
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 1
- BALXUFOVQVENIU-KXNXZCPBSA-N pseudoephedrine hydrochloride Chemical compound [H+].[Cl-].CN[C@@H](C)[C@@H](O)C1=CC=CC=C1 BALXUFOVQVENIU-KXNXZCPBSA-N 0.000 description 1
- 230000003014 reinforcing effect Effects 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 239000012266 salt solution Substances 0.000 description 1
- 229920002050 silicone resin Polymers 0.000 description 1
- 235000010344 sodium nitrate Nutrition 0.000 description 1
- 239000004317 sodium nitrate Substances 0.000 description 1
- VWDWKYIASSYTQR-UHFFFAOYSA-N sodium nitrate Inorganic materials [Na+].[O-][N+]([O-])=O VWDWKYIASSYTQR-UHFFFAOYSA-N 0.000 description 1
- 239000000758 substrate Substances 0.000 description 1
- 229920001059 synthetic polymer Polymers 0.000 description 1
Images
Classifications
-
- C—CHEMISTRY; METALLURGY
- C06—EXPLOSIVES; MATCHES
- C06C—DETONATING OR PRIMING DEVICES; FUSES; CHEMICAL LIGHTERS; PYROPHORIC COMPOSITIONS
- C06C5/00—Fuses, e.g. fuse cords
Definitions
- This invention relates to fusecord of the kind commonly employed for the transmission of detonation or flame in blasting and seismic prospecting operations.
- the invention also includes methods of manufacturing the fusecord.
- Such fusecord usually comprises a core of incendiary or explosive material surrounded by non-explosive wrapping materials, for example, textile yarns and/or synthetic plastics materials.
- detonating cord usually has a core comprising high explosive particles such as pentaerythritol tetranitrate (PETN) or cyclotrimethylene trinitramine (RDX)
- PETN pentaerythritol tetranitrate
- RDX cyclotrimethylene trinitramine
- safety fuse has a core which burns at a relatively slow rate and which usually comprises the well known black powder which is a mixture of charcoal, sodium or potassium nitrate and sulphur.
- the core is often encased in a thin envelope of paper or plastics film.
- thermoplastics sheath is usually derived from rubbers or polyurethanes or from a polymer or copolymer of vinyl chloride; or from an olefinic polymer such as polyetheylene and may be in a solid or cellular form.
- fusecords were sufficiently water impermeable to be used commercially and did, in fact, experience considerable commercial success.
- thermoplastic sheath component with additional strands of yarn which had been coated by a hot-melt process with wax which adheres the yarns, which may for example be cellulosic yarns such as rayon, to the thermoplastic sheath which very suitably may be polyethylene.
- the fusecords of the prior art and as described generally above are meritorious articles of commerce and for many purposes do not require to be modifed. However under certain conditions the prior art fusecords need modification to ensure that they may be used in a more reliable manner.
- adhesive waxes applied by the hot melt process undergo physical changes so that the surface of e fusecord becomes sticky or tacky, and under very hot conditions such wax components soften sufficiently to make it difficult to thread the fusecord through conventional detonating relay connectors.
- certain wax-treated outer strands tend to disintegrate or unwind and thereby producing an unsatisfactory fusecord.
- krown fusecords may be modified so as to provide improvements in their physical properties such as resistance to ab sion; or in their chemical resistance to the action o salt solutions, such as those obtained by the action of tier on ammonium nitrate; or to the effect of contac with carbonaceous materials such as fuel oil; or to the tackifying or sur- face softening effect induced by comparatively high ambient temperatures; or to the oxidation of the thermoplastic sheath induced by ultraviolet radation.
- Such modifications may be achieved if the coating of wax applied by a hot melt technique to the strands enclosing the thermoplastic sheath is replaced by an adhesive coating derived from a water-based composition and which is applied as a water-bearing adhesive to the strands and/or the enclosing thermoplastic sheath in an amount sufficient, and in a manner such, that adhesion between the said strands and the said sheath is obtained.
- thermoplastic sheath a part at least of which is enclosed by flexible strands the improvement wherein the said strands are adhered to-the said sheath by an adhesive component derived from a water-bearing adhesive compositon.
- the thermoplastic sheath may be derived from natural occurring materials or synthetic plastics materials. Compositions comprising synthetic or natural rubbers.
- thermoplastic sheath may be made from compositions comprising polyvinyl chloride especially plasticized polyvinyl chloride compositions.
- the flexible strands may take a variety of forms. Thus conveniently they may be in the form of fibres, yarns;, braids, tapes, textiles and the like and may be made from one or more components such as in conjugate fibres, or they be in the form of bulked or fibrillated fibres if desired. They may be derived from plant material such as jute or cotton or from cellulosic derivatives such as rayon. It is preferred however that the strands be derived from synthetic plastics material such as for example poly- efins, polyamides, polyacrylates or polyesters. Yarns, fibres, tapes or textiles derived from polyethylene or fibrillated polypropylene are useful and such products made from polyester such as polyethylene terephthalate are particularly useful.
- the flexible strands may be placed in position on the surface of the sheath by conventional means for example by the use of a spun layer and a countering layer of strands or by a braiding operation.
- a treatment such as a radiation treatment
- the strands may also be derived from compositions containing additives, such as for example additives which confer resistance to degradation of the strands to the effect of.heat or the effect of light such as ultraviolet light.
- the surface of the thermoplastic sheath may also be modified such as for example by treatment with radiation or an acidic solution, if desired.
- the adhesive component suitably may comprise polymeric or co-polymeric material inwater-bearing compositions of the structural adhesive type or of the holding adhesive type.
- structural adhesive type is meant a composition wherein the adhesive component holds two adherends and produces high strength in conditions of shear, tension or peel.
- holding adhesive type is meant a composition used primarily for attaching one adherend to another and holding it in place without requiring major significance to external stressing.
- Suitable adhesive compositions include air drying types in which the bonding agents are dispersed or dissolved in a liquid so as to permit the necessary flow during application to the adherend.
- Such adhesive compositions may be in a variety of physical forms, typically solutions, emulsions, dispersions, pastes or latexes, and it is preferred that the liquid contains water as a major constituent, and preferably as the sole constituent, of the liquid component of the adhesive composition.
- the nature of the polymeric or copolymeric material will vary to some extent on the nature of the sheath material and the strand material and in choosing the polymeric adhesive component care should be taken to ensure that a suitable bond can be formed between the adherends and the adhesive.
- Suitable adhesives may be derived from natural products such as gums or rubber, but it is preferred that they comprise synthetic compounds such as synthetic rubbers, epoxy resins, acrylic compounds, and the like.
- adhesives comprising unsaturated compounds are very useful, especially when they contain a vinyl group, and typical compounds of this class include vinyl polymers such as polyvinyl alcohol or polyvinyl acetate or copolymers derived from olefins, typically ethylene, and vinyl acetate.
- vinyl polymers such as polyvinyl alcohol or polyvinyl acetate or copolymers derived from olefins, typically ethylene, and vinyl acetate.
- the amount of adhesive components in the composition should be such that the composition can be applied without difficulty to the adherends; and dependent to some extent on the chemical and physical nature of the adhesive components it has been found that adhesive compositions containing from 10 to 80% w/w, preferably from 40 to 60% w/w, of adhesive component are satisfactory.
- thermoplastic sheath a part at least of which is enclosed by flexible strands the improvement wherein the said strands are adhered to the said sheath by treating the surfaces thereof with a water-bearing adhesive composition and removing the liquid component of the said composition.
- such a drying step may be performed in a drying tunnel wherein the partially completed, wet fusecord is passed through gas at an elevated temperature, for example air at a temperature between 90 and 105 C.
- an amount of adhesive composition can be applied to the surface of the sheath prior to spinning the first layer of strands, and/or subsequent to forming the counter layer of strands.
- the adhesive composition may be applied in various ways such as by pneumatic means using shaped nozzles, or by / guiding the partially completed fusecord through a reservoir of adhesive composition and controlling the rate of application of the composition by the use of one or more wiper dies. Yet again the adhesive composition may be sprayed on to the appropriate surfaces.
- the rate of application of the adhesive composition may be varied so as to provide the desired degree of bonding for a range of sizes of strands enclosing a range of sizes of sheaths. As a guide it has been found that a rate of application that provides from about 0.05 to about 5 grams of adhesive component per metre of length of the enclosed sheath is satisfactory for most fusecords.
- the fusecords of the invention are similar to fusecords of the prior art with the exception that the adhesive component in contact with the thermoplastic sheath and its enclosing strands is derived from a water-bearing adhesive composition.
- This modification has led to improvements in the fusecords as described hereinbefore, and additionally it has provided fusecords which facilitate the operation whereby knots may be tied and maintained in a tied con- dition in the fusecord.
- fusecords which have an economic advantage over similar fusecords of the prior art. In mining operations one of the key features which lead to the choice of a fusecord is the ease with which knots may be tied in fusecords and the extent to which such knots remain tight.
- This example illustrates a detonating cord. according to the invention and having a detonable core component comprising a particulate high explosive material which has been treated with a dialkyl ester of an aromatic dicarboxylic acid and wherein the thermoplastic sheath is derived from a plasticized polyvinyl chloride composition and wherein the flexible strands are polyester yarns.
- a detonable core component was prepared by adding 2 parts by weight of di-isooctyl phthalate (DIOP) to an agitated slurry of PETN (1000 parts) in aqueous acetone and the mixture so obtained was agitated until the di-isooctyl phthalate was mixed uniformly into the slurry and thereafter the diisooctylphthalate-treated PETN was separated from the slurry to provide a particulate high explosive material which contained approximately 0.2% w/w of DIOP.
- DIOP di-isooctyl phthalate
- a detonating cord depicted generally in Fig 1 was manufactured by a process wherein a detonable core component 1 comprising the particulate high explosive material made above was loaded from a hopper exit at a charge rate of 10 grams per metre into a tube 2 formed by convolution of a tape which was 16 millimetres wide and was fabricated from polyethylene terephthalate and available under the registered trade mark of "Melinex".
- a yarn material 3 which was formed from two yarns of twisted 470 decatex cotton was trained through the hopper exit and along the axis of the tube 2 to remain within the core 1.
- the tube 2 was surrounded by a spun layer 4 consisting of 8 yarns of 130 Tex polypropylene helically wound at 30 turns per metre and a countering layer 5 consisting of 10 yarns of 130 Tex polypropylene helically wound at 30 turns per metre.
- a polyvinylchloride composition available from ICI Australia Limited under the designation "Welvic” 50390-000 ("Welvic” is a registered trade mark) and containing a low volatility plasticizer, was extruded so as to coat the layer 5 with a layer of the "Welvic” composition to form a thermoplastic sheath 6 which weighed 3 grams per metre and the sheath was surrounded by a spun layer 7 consisting of 10 yarns of 80 Tex polyethylene terephthalate spun yarn helically wound at 46 turns per metre.
- a water-based adhesive composition having a viscosity of 22 poise and a pH value of 5.3, and available commercially from International Adhesives Pty Ltd of Sydney, Australia under the designation Type 272/1033.
- the adhesive component comprised a copolymer containing polyvinyl acetate and the composition contained 52% w/w of solids and had a density of 1.07 gram per cubic centimetre.
- the composition was applied at a rate of 3 grams per metre length of sheath 6.
- Excess adhesive was removed from the spun layer 7 by passing the partially completed detonating cord through a wiper die, a countering layer 9 consisting of 10 yarns of 80 Tex polyethyleneterephthalate spun yarn helically wound at 46 turns per metre was formed over the applied adhesive composition, and the product so obtained was passed through a drying tunnel, maintained at a temperature in a range from 95 to 105°C, for five minutes to remove the liquid components of the adhesive composition and to leave a bonding amount of adhesive 8 in contact with the sheath 6, and the yarns 7 and 9.
- the detonating cord so prepared had a surface.which was dry to the touch and it could be formed into a reel.
- This reeled detonating cord and a length of the same cord were stored for four weeks at a temperature in a range from 35 to 40°C and after this time the surface of the cord was similar to that of thesurface of the cord when freshly prepared.
- the stored detonating cord was knotted easily and the knots remained tight at an inspection eight hours after being made.
- Example 1 The general procedure of Example 1 was repeated except that in the present example the detonable core component 1 was crystalline PETN loaded at a charge rate of 10 grams per metre of length of tube, and the spun and counter yarns 7 and 9 of Example 1 were replaced by 16 braided yarns of 130 Tex polypropylene which were bonded to the thermoplastic sheath 6 by means of an adhesive component derived from the adhesive composition used in Example 1 and applied to the surface of the sheath 6 at a rate of 5 grams per metre of length of sheath 6. There was thus obtained a detonating cord according to the invention.
- FIG. 1 illustrates a safety fuse according to the invention and having a core comprising black powder and wherein the thermoplastic sheath is fabricated from foamed polyethylene and wherein the flexible strands were polyester yarns.
- a safety fuse depicted generally in Fig 2 was manufactured by a process wherein a core component 16 comprising black powder was loaded from a hopper exit at a charge rate of 4 grams per metre into a casing 20 which is provided by spinning ten fibres 22 of jute about the core 16 and subsequently forming a second layer of casing 20 by cross-spinning five fibres 22 of glass over the jute. Cotton filaments 18 were trained through the hopper exit and along the axis of casing 20 to remain within core 16.
- the partially completed prcduct 12 was coated with a polyethylene sheath 14 which had an internal cellular structure 26 and a substantially continuous outer skin 24.
- the 14 was applied by means used conventionally to extrude polyethylene in the form of a foam on to a substrate.
- the outer skin 24 of the sheath 14 was treated with the water-based adhesive 32 of Example 1 at a rate of 4 grams of composition per metre length of sheath 14 and a spun layer 30 of polyethylene terephthalate yarns was helically wound over the adhesively treated skin 24.
- a similar further application of adhesive 32 was made on to the surface of the yarns of spun layer 30 and a similar counter spun layer 33 of polyethylene terephthalate yarns was located cver the adhesive 32.
- the resultant product was passed through a stream of air heated at a temperature at 105°C to provide a fusecord having a dry surface comprising strands of polyethylene terephthalate bonded to the skin of a thermoplastic sheath by means of a copolymeric component derived from a water-bearing adhesive composition.
- Example 1 In this series of examples the general procedure of Example 1 was repeated except that the adhesive composition of that example was replaced by a range of compositions in which the characterizing adhesive component was as designated in Table 1 and wherein the major ingredient of the carrier component of the composition was water. Table 1 also shows the rate of application of the adhesive composition expressed as grams of composition per metre of sheath length. Each of the detonating cords so produced had surface, reeling, storage and knotting characteristics similar to the corresponding characteristic.of the detonating cord of Example 1.
- thermoplastic sheath was formed from a range of plasticized polyvinyl chloride compositions available from ICI Australia under a designation of "Welvic” followed by a numerical code. These various "Welvic" compositions are referred to in Table 2.
- the detonating cord so produced had a surface which was dry to the touch, it could be formed into a reel, and had storage and knotting characteristics similar to those of the detonating cord of Example 1.
- Example 2 In this series of examples the general procedure of Example 1 was repeated except that the thermoplastic sheath was derived from a composition the major component of which is set out in Table 3, which also describes the type of yarn used to prepare both the spun layer 7 and the countering layer 9 each of which layers contained 3 yarns.
- the detonating cord so produced had a surface which was dry to the touch, it could be formed into a reel and had storage and knotting characteristies similar to those of the detonating cord of Example 1.
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- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Multicomponent Fibers (AREA)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
AU1055/77 | 1977-08-01 | ||
AUPD105577 | 1977-08-01 |
Publications (2)
Publication Number | Publication Date |
---|---|
EP0000523A1 true EP0000523A1 (fr) | 1979-02-07 |
EP0000523B1 EP0000523B1 (fr) | 1982-06-16 |
Family
ID=3767111
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EP78100402A Expired EP0000523B1 (fr) | 1977-08-01 | 1978-07-14 | Cordeau et procédé de fabrication |
Country Status (9)
Country | Link |
---|---|
US (1) | US4230041A (fr) |
EP (1) | EP0000523B1 (fr) |
CA (1) | CA1117820A (fr) |
DE (1) | DE2861900D1 (fr) |
GB (1) | GB2001739B (fr) |
IT (1) | IT1158897B (fr) |
NZ (1) | NZ187824A (fr) |
ZA (1) | ZA784039B (fr) |
ZM (1) | ZM6878A1 (fr) |
Families Citing this family (15)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB9017715D0 (en) * | 1990-08-13 | 1990-09-26 | Ici Plc | Low energy fuse |
US5658414A (en) * | 1995-03-03 | 1997-08-19 | Kraft Foods, Inc. | Organometallic solvent seaming of cellulosic materials |
US5690777A (en) * | 1995-03-03 | 1997-11-25 | Kraft Foods, Inc. | Seamed cellulosic materials using organometallic solvents |
US5939661A (en) * | 1997-01-06 | 1999-08-17 | The Ensign-Bickford Company | Method of manufacturing an explosive carrier material, and articles containing the same |
US5864084A (en) * | 1997-04-16 | 1999-01-26 | American Promotional Events, Inc. | Glow in the dark fuse and method for making same |
US6247410B1 (en) * | 1998-12-10 | 2001-06-19 | The United States Of America As Represented By The Secretary Of The Navy | High-output insensitive munition detonating cord |
GB9913262D0 (en) * | 1999-06-09 | 2002-08-21 | Royal Ordnance Plc | Desensitation of energetic materials |
US6439099B1 (en) | 2000-09-14 | 2002-08-27 | The United States Of America As Represented By The Secretary Of The Navy | Explosive charges braided into a line charge assembly |
JP4342443B2 (ja) * | 2002-09-10 | 2009-10-14 | 株式会社クラベ | コード状温度ヒューズと面状温度ヒューズ |
US20090217811A1 (en) * | 2006-01-17 | 2009-09-03 | David William Leeming | Textile armour |
NL2000406C2 (nl) * | 2006-12-22 | 2008-06-24 | Tno | Werkwijze en inrichting voor het beschermen van objecten tegen raket-aangedreven granaten (RPG's). |
DE102009050084A1 (de) * | 2009-10-20 | 2011-07-28 | Fasel, Albert, 65520 | Mehrschichtiger Schlauch mit einer schlauchförmigen Innenfolie, Vorrichtung und Verfahren zu dessen Herstellung sowie dessen Verwendung |
CN105674807B (zh) * | 2014-11-19 | 2017-08-04 | 南京理工大学 | 一种基于sy导爆索装药的起爆索 |
CN109667007B (zh) * | 2017-10-17 | 2022-03-25 | 喻翠云 | 一种新型微烟引火线外包线的制备方法及应用 |
KR20230102736A (ko) * | 2021-12-30 | 2023-07-07 | 주식회사 한화 | 기폭신호 전달용 쇼크튜브 및 그 제조방법 |
Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB1016404A (en) * | 1963-11-15 | 1966-01-12 | Ensign Bickford Co | Fuse |
FR2198116A1 (fr) * | 1972-09-06 | 1974-03-29 | Ici Ltd | |
US3945320A (en) * | 1973-07-04 | 1976-03-23 | Imperial Chemical Industries Limited | Water-resistant fuse-cord |
Family Cites Families (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB471433A (en) | 1936-03-03 | 1937-09-03 | James Sinton Bruce Fleming | Improvements in or relating to the manufacture of safety fuze |
GB1070660A (en) * | 1964-12-30 | 1967-06-01 | Ici Ltd | Manufacture of granular pentaerythritol tetranitrate |
US3318242A (en) * | 1965-06-23 | 1967-05-09 | Trojan Powder Co | Packaged explosive product |
GB1106396A (en) * | 1965-08-19 | 1968-03-13 | Du Pont | Explosive composition |
US3428502A (en) * | 1966-10-25 | 1969-02-18 | Du Pont | Polyvinyl acetate binder for crystalline explosive |
US3881420A (en) * | 1971-09-23 | 1975-05-06 | Ensign Bickford Co | Smoke cord |
US3908509A (en) * | 1973-10-29 | 1975-09-30 | Eb Ind Inc | Fuse and its method of manufacture |
GB1456281A (en) | 1974-04-22 | 1976-11-24 | Ici Ltd | Detonating fuse-cord |
US3995525A (en) * | 1974-05-20 | 1976-12-07 | Imperial Chemical Industries Limited | Method for manufacturing detonating fuse-cord |
-
1978
- 1978-07-10 NZ NZ187824A patent/NZ187824A/xx unknown
- 1978-07-12 US US05/924,064 patent/US4230041A/en not_active Expired - Lifetime
- 1978-07-14 DE DE7878100402T patent/DE2861900D1/de not_active Expired
- 1978-07-14 EP EP78100402A patent/EP0000523B1/fr not_active Expired
- 1978-07-17 ZA ZA784039A patent/ZA784039B/xx unknown
- 1978-07-24 ZM ZM68/78A patent/ZM6878A1/xx unknown
- 1978-07-25 GB GB787831087A patent/GB2001739B/en not_active Expired
- 1978-07-28 IT IT26283/78A patent/IT1158897B/it active
- 1978-07-28 CA CA000308375A patent/CA1117820A/fr not_active Expired
Patent Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB1016404A (en) * | 1963-11-15 | 1966-01-12 | Ensign Bickford Co | Fuse |
FR2198116A1 (fr) * | 1972-09-06 | 1974-03-29 | Ici Ltd | |
US3945320A (en) * | 1973-07-04 | 1976-03-23 | Imperial Chemical Industries Limited | Water-resistant fuse-cord |
Also Published As
Publication number | Publication date |
---|---|
ZA784039B (en) | 1980-03-26 |
CA1117820A (fr) | 1982-02-09 |
GB2001739A (en) | 1979-02-07 |
US4230041A (en) | 1980-10-28 |
EP0000523B1 (fr) | 1982-06-16 |
ZM6878A1 (en) | 1980-06-20 |
GB2001739B (en) | 1982-01-06 |
IT7826283A0 (it) | 1978-07-28 |
NZ187824A (en) | 1980-08-26 |
IT1158897B (it) | 1987-02-25 |
DE2861900D1 (en) | 1982-08-05 |
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