US1341705A - Detonating-fuse - Google Patents

Detonating-fuse Download PDF

Info

Publication number
US1341705A
US1341705A US301771A US30177119A US1341705A US 1341705 A US1341705 A US 1341705A US 301771 A US301771 A US 301771A US 30177119 A US30177119 A US 30177119A US 1341705 A US1341705 A US 1341705A
Authority
US
United States
Prior art keywords
trinitrotoluene
cordeau
tetryl
detonating
fuse
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 - Lifetime
Application number
US301771A
Inventor
Willard C Cope
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
EIDP Inc
Original Assignee
EI Du Pont de Nemours and Co
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by EI Du Pont de Nemours and Co filed Critical EI Du Pont de Nemours and Co
Priority to US301771A priority Critical patent/US1341705A/en
Application granted granted Critical
Publication of US1341705A publication Critical patent/US1341705A/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C06EXPLOSIVES; MATCHES
    • C06BEXPLOSIVES OR THERMIC COMPOSITIONS; MANUFACTURE THEREOF; USE OF SINGLE SUBSTANCES AS EXPLOSIVES
    • C06B25/00Compositions containing a nitrated organic compound
    • C06B25/04Compositions containing a nitrated organic compound the nitrated compound being an aromatic
    • C06B25/06Compositions containing a nitrated organic compound the nitrated compound being an aromatic with two or more nitrated aromatic compounds present

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Fuses (AREA)

Description

. No Drawing.
WILLARD 0. corner woonB nY, new annsnnnssrencn Ton. I,,Du r on'r ,DE .1 In- M 1135 & some O WILMINGTQM eWfi-B A QQRPORATION OF DELA AR DET-QNATING-FU-SE.
To all whom it may concern:
Be it known that I, WILLARD C. Corn, a citizen of the United States, and a resident of lVoodbury, in the county of Gloucester and State of New Jersey, have invented a certain new and useful Detonating-F use, of which the following is a specification.
This invention relates to new detonating fuses and comprises a detonating fuse (socalled cordeau) in which the detonating composition consists essentially of a mixture of 2.4.(ltrinitrophenyl-methyl-nitramm (tetryl) and trinitrotoluene.
Hitherto, cordeau has been made by filling a metallic (usually lead) pipe of suitable size, say 1}" diameter, with molten trinitrotoluene, allowing this to solidify and subsequently reducing the diameter of the plpe by passing through a series of rolls. In place of the trinitrotoluene, other explosives, such as picric acid, have been suggested. Practically all of these other explosives, however, are diflicult to work with since they melt at a relatively high temperature and hence are not capable of easy manipulation, or they form undesirable sensitive salts with the metallic envelop. T rinitrotoluene alone makes fairly satisfactory cordeau but unless the trinitrotoluene is absolutely pure, the cordeau deteriorates with age, becoming insensitive to detonation and eventually incapable of propagating detonation and hence useless for the various purposes for which cordeau is used. Furthermore, pure trinitrotoluene is difiicult and expensive to make.
I have discovered that by substituting for pure trinitrotoluene a mixture of trinitrotoluene and tetryl, cordeau may be manufactured which has many advantages over cordean made with trinitrotoluene alone. The proportions in which I may use tetryl and trinitrotoluene are capable of wide variation. I may with advantage use as little as 2% tetryl or as much as 75%.
The effect of tetryl is to raise the velocity pf detonation of the cordeau and also to avoid the deterioration which occurs when cordeau is made with trinitrotoluene alone. Another advantage in the use of tetryl is that I am able to use an inferior grade of trinitrotoluene which is more easily and cheaply produced than pure trinitrotoluene.
By varying the percentage of tetryl, I am able to produce cordeau having various ve- 7 Patented June 1, 1920.
Application filed June 4, 1819. Serial 310.801,?71.
locities of detonation. Cordeau made with trinitrotoluene alone will have a velocity of detonation of from 5000 to 5500 meters per second. lVith various percentages of tetryl, velocities of detonation from 5500 to 6800-meters per second are obtainable.
Tetryl alone cannot be used in cordeau with complete satisfaction because it decon1- poses at or slightly above its melting point and hence cannot be easily manipulated in the manufacture of cordeau.
The manufacture of cordeau according to my new process may be illustrated by the following specific example :Trinitrotoluene is melted and tetryl in suitable proportions is thoroughly mixed therewith; if desired the ingredients may be mixed together in the solid condition and then melted. The proportions which I prefer to use ordinarily are 80 parts of trinitrotoluene to 20 parts of tetryl. The resulting fluid mixture is then introduced into a lead pipe of about 111' diameter, and allowed to solidify therein. The pipe is then passed through a series of rolls until the diameter of the pipe has been reduced to the desired extent.
Tetryl is soluble in trinitrotoluene to the extent of somewhat more than 50%. In addition to this 50%, approximately 25% more may be suspended in the solution of tetryl and trinitrotoluene, thus forming a mush, which can still be handled as a liquid and hence can be easily manipulated in the operations incident to the manufacture of cordeau. Increasing the percentage of tetryl has the effect of making the mixture more sensitive to detonation and of raising its velocity of detonation. V
The new cordeau detonant, and especially that containing about 20 of tetryl, has the following advantages: (1) It is safe to work with; (2) it is easier to manipulate during the rolling operation than cordeau made with trinitrotoluene alone; (3) it has a higher velocity than cordeau made with trinitrotoluene alone ;'and (4) it does not deteriorate on storage as is the case when trinitrotoluene alone is used.
I claim:
1. A detonating fuse having a detonating mixture comprising trinitrophenyl-methylnitramin and trinitrotoluene.
2. A detonating fuserconsisting of a metallic tube containing a detonating mixture comprising trinitrotoluene and trinitorphcnyl-methyl-nitramin, the latter forming from 2 to 75% of the mixture.
3. A detonating fuse consisting of a metallic tube containing a detonating mixture comprising about 80 parts of trinitrotoluene and about 20 parts of trinitrophenyl-methylnitramin.
4. A fuse detonant comprising trinitropheny1-methy1-nitramin mixed with trini- 10 trotoluene.
5. A fuse detonant comprising a homogenous mixture of trinitrophenyl-methy1-ni tramin and trinitrotoluene, the amount of the former being from 2 to 75% of the mixture.
6. A fuse detonant comprising a mixture containing trinitrotoluene and about 20% of trinitrophenyl-meth l-nitramin.
In testimony whereo I aflix my signature.
WILLARD G. COPE.
US301771A 1919-06-04 1919-06-04 Detonating-fuse Expired - Lifetime US1341705A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
US301771A US1341705A (en) 1919-06-04 1919-06-04 Detonating-fuse

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US301771A US1341705A (en) 1919-06-04 1919-06-04 Detonating-fuse

Publications (1)

Publication Number Publication Date
US1341705A true US1341705A (en) 1920-06-01

Family

ID=23164798

Family Applications (1)

Application Number Title Priority Date Filing Date
US301771A Expired - Lifetime US1341705A (en) 1919-06-04 1919-06-04 Detonating-fuse

Country Status (1)

Country Link
US (1) US1341705A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2482090A (en) * 1944-03-20 1949-09-20 Us Sec War Method of making a high-density explosive
US2482089A (en) * 1944-03-20 1949-09-20 Us Sec War Method of making a high-density explosive

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2482090A (en) * 1944-03-20 1949-09-20 Us Sec War Method of making a high-density explosive
US2482089A (en) * 1944-03-20 1949-09-20 Us Sec War Method of making a high-density explosive

Similar Documents

Publication Publication Date Title
US2063572A (en) Process of preparing explosive charges
US3212945A (en) Production of detonatable explosive emulsion preparations
US4600452A (en) Eutectic microknit composite explosives and processes for making same
US1341705A (en) Detonating-fuse
US2450892A (en) Delay powder
US1890112A (en) Igniter charge for blasting caps
US3306789A (en) Nitric acid explosive composition containing inorganic nitrate oxidizer and nitrated aromatic compound
US2322416A (en) Flux
US3249476A (en) Composition of low crystalization point and method of preparation
US2371879A (en) Explosive charge
US1964077A (en) Flash composition
US2493551A (en) Production of normal lead dinitroresorcinate
US2131574A (en) Explosive
US2257360A (en) Desensitized pentaerythritol tetranitrate explosive
US1922123A (en) Inulin nitrate and method of producing
DE349724C (en) Process for increasing the density or for gelatinizing explosives
US249701A (en) Explosive compound
US1964755A (en) Explosive composition
US4432819A (en) Priming composition and techniques
DE1771480B1 (en) Water-based explosives mixture
US2021497A (en) Lead salts of dinitrosalicylic acid
GB142898A (en) Improvements in explosives
US1201191A (en) Ignitible compound for matches.
US2038097A (en) Priming mixture
US2081161A (en) Sucrose octanitrate