USH925H - Encapsulated signal illumination flare composition - Google Patents
Encapsulated signal illumination flare composition Download PDFInfo
- Publication number
- USH925H USH925H US07/440,065 US44006589A USH925H US H925 H USH925 H US H925H US 44006589 A US44006589 A US 44006589A US H925 H USH925 H US H925H
- Authority
- US
- United States
- Prior art keywords
- weight percent
- flare
- composition
- comprised
- capsules
- 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.)
- Abandoned
Links
- 239000000203 mixture Substances 0.000 title claims abstract description 39
- 238000005286 illumination Methods 0.000 title 1
- 239000002775 capsule Substances 0.000 claims abstract description 23
- 239000011230 binding agent Substances 0.000 claims abstract description 22
- 230000001070 adhesive effect Effects 0.000 claims abstract description 18
- 239000000853 adhesive Substances 0.000 claims abstract description 17
- 239000004615 ingredient Substances 0.000 claims abstract description 15
- VWDWKYIASSYTQR-UHFFFAOYSA-N sodium nitrate Chemical compound [Na+].[O-][N+]([O-])=O VWDWKYIASSYTQR-UHFFFAOYSA-N 0.000 claims abstract description 14
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 claims abstract description 12
- 238000002156 mixing Methods 0.000 claims abstract description 12
- 108010010803 Gelatin Proteins 0.000 claims abstract description 11
- 235000010489 acacia gum Nutrition 0.000 claims abstract description 11
- 239000001785 acacia senegal l. willd gum Substances 0.000 claims abstract description 11
- 229920000159 gelatin Polymers 0.000 claims abstract description 11
- 239000008273 gelatin Substances 0.000 claims abstract description 11
- 235000019322 gelatine Nutrition 0.000 claims abstract description 11
- 235000011852 gelatine desserts Nutrition 0.000 claims abstract description 11
- IISBACLAFKSPIT-UHFFFAOYSA-N bisphenol A Chemical compound C=1C=C(O)C=CC=1C(C)(C)C1=CC=C(O)C=C1 IISBACLAFKSPIT-UHFFFAOYSA-N 0.000 claims abstract description 10
- 210000002421 cell wall Anatomy 0.000 claims abstract description 10
- 239000000843 powder Substances 0.000 claims abstract description 9
- 239000011777 magnesium Substances 0.000 claims abstract description 8
- 229910052749 magnesium Inorganic materials 0.000 claims abstract description 8
- 239000004317 sodium nitrate Substances 0.000 claims abstract description 7
- 235000010344 sodium nitrate Nutrition 0.000 claims abstract description 7
- 229920000728 polyester Polymers 0.000 claims abstract description 5
- 239000004342 Benzoyl peroxide Substances 0.000 claims abstract description 4
- OMPJBNCRMGITSC-UHFFFAOYSA-N Benzoylperoxide Chemical compound C=1C=CC=CC=1C(=O)OOC(=O)C1=CC=CC=C1 OMPJBNCRMGITSC-UHFFFAOYSA-N 0.000 claims abstract description 4
- 235000019400 benzoyl peroxide Nutrition 0.000 claims abstract description 4
- GYZLOYUZLJXAJU-UHFFFAOYSA-N diglycidyl ether Chemical compound C1OC1COCC1CO1 GYZLOYUZLJXAJU-UHFFFAOYSA-N 0.000 claims abstract description 4
- 239000011344 liquid material Substances 0.000 claims abstract description 4
- 229920001225 polyester resin Polymers 0.000 claims abstract description 4
- 239000004645 polyester resin Substances 0.000 claims abstract description 4
- 229920000642 polymer Polymers 0.000 claims abstract description 4
- 229920006332 epoxy adhesive Polymers 0.000 claims abstract 4
- 238000004519 manufacturing process Methods 0.000 claims description 11
- 238000000034 method Methods 0.000 claims description 10
- 238000005029 sieve analysis Methods 0.000 claims description 3
- 238000003801 milling Methods 0.000 claims 1
- 239000002245 particle Substances 0.000 claims 1
- 238000005303 weighing Methods 0.000 claims 1
- 230000035945 sensitivity Effects 0.000 description 5
- 238000010586 diagram Methods 0.000 description 4
- 239000000463 material Substances 0.000 description 3
- KUBDPQJOLOUJRM-UHFFFAOYSA-N 2-(chloromethyl)oxirane;4-[2-(4-hydroxyphenyl)propan-2-yl]phenol Chemical compound ClCC1CO1.C=1C=C(O)C=CC=1C(C)(C)C1=CC=C(O)C=C1 KUBDPQJOLOUJRM-UHFFFAOYSA-N 0.000 description 2
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 2
- 239000008188 pellet Substances 0.000 description 2
- 238000012545 processing Methods 0.000 description 2
- 238000012360 testing method Methods 0.000 description 2
- BRLQWZUYTZBJKN-UHFFFAOYSA-N Epichlorohydrin Chemical compound ClCC1CO1 BRLQWZUYTZBJKN-UHFFFAOYSA-N 0.000 description 1
- 239000004593 Epoxy Substances 0.000 description 1
- 238000004140 cleaning Methods 0.000 description 1
- 238000005354 coacervation Methods 0.000 description 1
- 239000007859 condensation product Substances 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 231100001261 hazardous Toxicity 0.000 description 1
- 238000012423 maintenance Methods 0.000 description 1
- 239000002861 polymer material Substances 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000004408 titanium dioxide Substances 0.000 description 1
Images
Classifications
-
- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F42—AMMUNITION; BLASTING
- F42B—EXPLOSIVE CHARGES, e.g. FOR BLASTING, FIREWORKS, AMMUNITION
- F42B4/00—Fireworks, i.e. pyrotechnic devices for amusement, display, illumination or signal purposes
- F42B4/26—Flares; Torches
-
- C—CHEMISTRY; METALLURGY
- C06—EXPLOSIVES; MATCHES
- C06B—EXPLOSIVES OR THERMIC COMPOSITIONS; MANUFACTURE THEREOF; USE OF SINGLE SUBSTANCES AS EXPLOSIVES
- C06B21/00—Apparatus or methods for working-up explosives, e.g. forming, cutting, drying
- C06B21/0008—Compounding the ingredient
- C06B21/0025—Compounding the ingredient the ingredient being a polymer bonded explosive or thermic component
-
- C—CHEMISTRY; METALLURGY
- C06—EXPLOSIVES; MATCHES
- C06C—DETONATING OR PRIMING DEVICES; FUSES; CHEMICAL LIGHTERS; PYROPHORIC COMPOSITIONS
- C06C15/00—Pyrophoric compositions; Flints
Definitions
- the present method for signal flare manufacture involves using a high-shear muller type mixer because the binder is viscous and highly adhesive.
- the use of a cured Laminac 4116 type binder even with mixing performed with a muller type mixer makes mixing difficult, and particularly, homogeneity of the ingredients is difficult to achieve.
- the mixing problems are attributed to the highly viscous and adhesive properties of the Laminac 4116 type binder. Because of the employment of this method of mixing, loss of materials due to hang-ups, time consumed in cleaning and equipment, and batch mixing due to the short potlife of the binder are contributing factors to substantial capital expenditures.
- the object of this novel method for the manufacture of signal illuminant flare compositions is to provide an encapsulated binder whereby the flare ingredients of magnesium powder, sodium nitrate, and an capsulated adhesive are blended to achieve homogeneity of ingredients prior to feeding into a flare press.
- the binder capsules are crushed and the other ingredients, sodium nitrate and magnesium are bonded into a solid flare mass.
- the instant invention involves the use of PEF-12 capsular adhesive without the titanium dioxide filer.
- This material is manufactured by the National Cash Register Company.
- the adhesive consists of two separate capsules which are blended together.
- One capsule contains the condensation products of epichlorohydrin and Bisphenol A or diglycidyl ether of Bisphenol A (EPON 828) 79% with 12% benzoyl peroxide.
- the second capsule contains Aropol 72-40-MC polyester resin with 5% N,N'-dimethyl-o-toluidine as the cure accelerator.
- the cell walls of both capsules are composed of Arabic gum and gelatin. They are produced using the coacervation technique.
- the capsules are blended in the order of one part epoxy capsule to two parts polyester capsule. The capsule sizes range from 300-1000 micrometers. When blended together, the capsules form a blend which performs as a free-flow powder containing 91% liquid materials with cell walls composed of about 9% Arabic gum and gelatin.
- the encapsulated illuminant compositions are manufactured by dry blending magnesium powder, sodium nitrate and the encapsulating binder.
- a quantity of flare increment is supplied by a flare increment feeder to a compacting flare press.
- the force of the compacting press causes rupture of the capsules, and the hydrualic force causes the polymers to mix, and surround the powders resulting in a very homogeneous mass.
- the illuminant compositions are compacted into paper containers (31-mm in diameter and 64-mm long) similarly to the standard M127A1 Hand-Held Signal Illuminants.
- the candles were compacted in two increments, 14,000 psi and cured for 16 hours at a minimum temperature of 170° F.
- FIG. 1 depicts flare burning rate, inches per second (ips), as influenced by magnesium and binder content.
- FIG. 2 depicts candlepower output as influenced by magnesium and binder content.
- FIG. 3 depicts a flow diagram for manufacture of M127A1 illuminant flares in accordance with prior art manufacturing sequences.
- FIG. 4 depicts a flow diagram for the manufacture of encapsulated signal illuminant flares.
- the signal illuminant flare composition prepared in accordance with this invention employs a capsular adhesive composition as the binder in two separate capsules which are blended in equal amounts together to form blend which performs as a free-flow powder containing 91% liquid material.
- the capsules are ruptured when subjected to the force of the compacting press used to consolidate the flare composition, and the resulting hydraulic forces causes the curable polymer to mix and surround the powders resulting in a very homogeneous mass.
- a crush resistant strength test was used to compare the mechanical properties of this illuminant. This involved the preparation of 20-gram samples which are consolidated at 14,000 psi in a 1.0 inch diameter die.
- the reference for evaluation was the standard illuminant composition which had been cured for 10 days at ambient temperature. Ballistic compositions of illuminant ammunition which had been cured under these conditions have performed satisfactorily, and, therefore, the crush strength measured on these standards has been defined as adequate.
- the encapsulated binder pellets demonstrated better crush strength over the temperature range of -65° F. to +160° F. than the standard pellets based on Laminac 4116.
- Friction and drop sensitivity tests were conducted to determine the safety characteristics of these Illuminants.
- the drop sensitivity of the illuminant containing the encapsulated ingredients were determined to be less sensitive than the standard M127A1 illuminant.
- the M127A1 illuminant had a drop sensitivity of 19 inches with a 4 pound ball.
- the illuminant containing the encapsulated binder had a drop sensitivity of 30 inches with a 4 pound ball.
- FIG. 3 A flow diagram for the manufacture of M127A1 signal illuminant flares is depicted in FIG. 3, and the flow diagram for the manufacture of encapsulated signal illuminant flares is depicted in FIG. 4.
Landscapes
- Engineering & Computer Science (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- General Engineering & Computer Science (AREA)
- Metallurgy (AREA)
- Dental Tools And Instruments Or Auxiliary Dental Instruments (AREA)
Abstract
An encapsulated signal illuminant flare composition is comprised of powde magnesium from about 45 to about 60 weight percent, of powdered sodium nitrate from about 32 to about 49 weight percent, and of capsular adhesives containing about 91 weight liquid materials contained within capsules having cell walls of equal parts Arabic gum and gelatin of about 9 weight percent to yield a binder from about 6 to about 12 weight percent. The composition ingredients are blended in a dry mixer to achieve a homogeneously, blended signal illuminant flare composition. The blended signal illuminant flare composition is incrementally fed into a flare press for compacting into cartridges in two increments at about 14,000 psi pressure which ruptures the capsular adhesives by hydraulic forces to achieve polymer mixing and the surrounding of the powder ingredients with the binder ingredients to form a very homogenous signal illuminant flare composition mass. The flare composition mass is cured for about 16 hours at a minimum temperature of about 170° F. The capsular adhesives are blended of about one part of an epoxy adhesive to two parts of a polyester adhesive. The capsular epoxy adhesive is comprised of about 79 weight percent diglycidyl ether of Bisphenol A and of about 12 weight percent of benzoyl peroxide contained in capsules having cell walls comprised of Arabic gum and gelatin of about 9 weight percent. The capsular polyester adhesive is comprised of about 86 weight percent polyester resin, of about 5 weight percent N, N'-dimethyl-o-toluidine contained in capsules having cell walls comprised of Arabic gum and gelatin of about 9 weight percent.
Description
The invention described herein may be manufactured, used, and licensed by or for the Government for governmental purposes without the payment to me of any royalties thereon.
The present method for signal flare manufacture involves using a high-shear muller type mixer because the binder is viscous and highly adhesive. The use of a cured Laminac 4116 type binder even with mixing performed with a muller type mixer makes mixing difficult, and particularly, homogeneity of the ingredients is difficult to achieve. The mixing problems are attributed to the highly viscous and adhesive properties of the Laminac 4116 type binder. Because of the employment of this method of mixing, loss of materials due to hang-ups, time consumed in cleaning and equipment, and batch mixing due to the short potlife of the binder are contributing factors to substantial capital expenditures.
The object of this novel method for the manufacture of signal illuminant flare compositions is to provide an encapsulated binder whereby the flare ingredients of magnesium powder, sodium nitrate, and an capsulated adhesive are blended to achieve homogeneity of ingredients prior to feeding into a flare press. When the specified ingredients are pressed in the flare-producing press, the binder capsules are crushed and the other ingredients, sodium nitrate and magnesium are bonded into a solid flare mass.
The instant invention involves the use of PEF-12 capsular adhesive without the titanium dioxide filer. This material is manufactured by the National Cash Register Company. The adhesive consists of two separate capsules which are blended together. One capsule contains the condensation products of epichlorohydrin and Bisphenol A or diglycidyl ether of Bisphenol A (EPON 828) 79% with 12% benzoyl peroxide. The second capsule contains Aropol 72-40-MC polyester resin with 5% N,N'-dimethyl-o-toluidine as the cure accelerator. The cell walls of both capsules are composed of Arabic gum and gelatin. They are produced using the coacervation technique. The capsules are blended in the order of one part epoxy capsule to two parts polyester capsule. The capsule sizes range from 300-1000 micrometers. When blended together, the capsules form a blend which performs as a free-flow powder containing 91% liquid materials with cell walls composed of about 9% Arabic gum and gelatin.
The encapsulated illuminant compositions are manufactured by dry blending magnesium powder, sodium nitrate and the encapsulating binder. A quantity of flare increment is supplied by a flare increment feeder to a compacting flare press. The force of the compacting press causes rupture of the capsules, and the hydrualic force causes the polymers to mix, and surround the powders resulting in a very homogeneous mass.
The illuminant compositions are compacted into paper containers (31-mm in diameter and 64-mm long) similarly to the standard M127A1 Hand-Held Signal Illuminants. The candles were compacted in two increments, 14,000 psi and cured for 16 hours at a minimum temperature of 170° F.
FIG. 1 depicts flare burning rate, inches per second (ips), as influenced by magnesium and binder content.
FIG. 2 depicts candlepower output as influenced by magnesium and binder content.
FIG. 3 depicts a flow diagram for manufacture of M127A1 illuminant flares in accordance with prior art manufacturing sequences.
FIG. 4 depicts a flow diagram for the manufacture of encapsulated signal illuminant flares.
The signal illuminant flare composition prepared in accordance with this invention employs a capsular adhesive composition as the binder in two separate capsules which are blended in equal amounts together to form blend which performs as a free-flow powder containing 91% liquid material. The capsules are ruptured when subjected to the force of the compacting press used to consolidate the flare composition, and the resulting hydraulic forces causes the curable polymer to mix and surround the powders resulting in a very homogeneous mass.
TABLE 1 ______________________________________ CAPSULAR ADHESIVE COMPOSITION* Capsule No Content Weight Percent ______________________________________ 1 Diglycidyl ether 79.0 of Bisphenol A** Benzoyl peroxide 12.0 Arabic gum and gelatin (1:1) 9.0 100.0 2 Polyester resin*** 86.0 .sub.-- N, .sub.-- N'-dimethyl- -o-toluidine 5.0 Arabic gum and gelatin (1:1) 9.0 100.0 ______________________________________ *PEF-12- Manufactured hy National Cash Register Company **EPON 828 ***Aropol 7240-MC
The percentage of binder, and the magnesium content, which are incorporated in the illuminant compositions influence the burning rate and the candlepower output thereof. These data are presented in Table 2 below and illustrated graphically in FIGS. 1 and 2.
TABLE 2 ______________________________________ EFFECT OF BINDER AND MAGNESIUM CONTENTS ON FLARE BURNING RATE AND CANDLEPOWER Binder Mg Density Burning Mix No. (%) (%) (gm/cc) Rate (IPS)* Candlepower ______________________________________ 1 6 45 1.808 0.0640 137,400 2 6 50 1.762 0.0799 173,300 3 6 55 1.707 0.0996 202,400 4 6 57 1.686 0.1119 201,400 5 8 45 1.847 0.0573 127,400 6 8 50 1.794 0.0748 151,100 7 8 55 1.754 0.0966 161,400 8 8 60 1.696 0.1110 161,700 9 10 45 1.858 0.0580 101,800 10 10 50 1.815 0.0730 119,500 11 10 55 1.764 0.0870 130,900 12 10 60 1.728 0.0996 126,600 13 12 50 1.863 0.0548 115,100 14 12 55 1.787 0.0752 103,800 ______________________________________ Notes: *IPS = inches per second 1. Illuminant weight = 85 grams 2. Magnesium powder -30/50 micrometers weightmeans-diameter by sieve analysis 3. Sodium nitrate -20micrometers weightmean-diameter by Fisher Subsieve sizer; 55micrometers weightmean-diameter by sieve analysis
A crush resistant strength test was used to compare the mechanical properties of this illuminant. This involved the preparation of 20-gram samples which are consolidated at 14,000 psi in a 1.0 inch diameter die. The reference for evaluation was the standard illuminant composition which had been cured for 10 days at ambient temperature. Ballistic compositions of illuminant ammunition which had been cured under these conditions have performed satisfactorily, and, therefore, the crush strength measured on these standards has been defined as adequate. The encapsulated binder pellets demonstrated better crush strength over the temperature range of -65° F. to +160° F. than the standard pellets based on Laminac 4116.
Friction and drop sensitivity tests were conducted to determine the safety characteristics of these Illuminants. The drop sensitivity of the illuminant containing the encapsulated ingredients were determined to be less sensitive than the standard M127A1 illuminant. The M127A1 illuminant had a drop sensitivity of 19 inches with a 4 pound ball. The illuminant containing the encapsulated binder had a drop sensitivity of 30 inches with a 4 pound ball. Thus, the safety aspects which would result from the adoption of the illuminant containing the encapsulated binder would be lower impact sensitivity, reduced safety hazards in manufacture, significant capital cost savings and manufacturing costs.
A flow diagram for the manufacture of M127A1 signal illuminant flares is depicted in FIG. 3, and the flow diagram for the manufacture of encapsulated signal illuminant flares is depicted in FIG. 4.
The mechanism of capsular rupturing of the two component capsular adhesive or the curable polymer materials defined in Table I provides a unique means for mixing and consolidating materials for signal illuminant flares. In addition to the fact that this new process offers ease of manufacture, other benefits derived include the following:
a. Savings in capital equipment,
b. Improved safety,
c. Reduced exposure of personnel to hazardous operations,
d. Continuous processing instead of bath processing, and
e. Lower operating/maintenance costs.
Claims (2)
1. A method for the manufacture of a signal illuminant utilizing a signal illuminant flare composition wherein the binder composition of said signal illuminant flare composition is formed from ingredients released from ruptured capsules during the mixing procedure, said capsules having cell walls comprised of Arabic gum and gelatin for containing the ingredients for forming said binder composition and wherein said capsules flow as a free-flow powder until subjected to a compacting force which ruptures the cell walls during a mixing procedure to thereby release said ingredients, said method comprising:
(i) feeding milled sodium nitrate into a hammer mill and milling the same to a powder to achieve a particle size from about 20 micrometers to about 55 micrometers weight-mean-diameter by sieve analysis;
(ii) admitting said milled sodium nitrate from a weighing feeder to an operating dry mixer in a weight percent range from about 32 to about 49 of said signal illuminant flare compositions which is additionally comprised of magnesium powder of about 30 to about 50 weight-mean-diameter in an amount from about 45 weight percent to about 60 weight percent of said signal illuminant flare composition and said binder composition from about 6 to about 12 weight percent of said signal illuminant flare composition;
(iii) admitting said magnesium powder to said operating dry mixer in a weight percent range from about 45 to about 60 of said signal illuminant flare composition;
(iv) blending capsular adhesives ranging in sizes from about 300 to about 1000 micrometers in a ratio of one part of an epoxy adhesive to two parts of a polyester adhesive to achieve when blended, a blend which performs as a free-flow powder containing 91% liquid materials contained within capsules having cell walls composed of about 9% Arabic gum and gelatin in equal ratio amounts, said epoxy adhesive comprised of about 79.0 weight percent diglycidyl ether of Bisphenol A and of about 12.0 weight percent of benzoyl peroxide contained in capsules having cell walls comprised of said Arabic gum and gelatin of about 9.0 weight percent, said polyester adhesive comprised of about 86.0 weight percent polyester resin and of about 5.0 weight percent N,N'-dimethyl-o-toluidine contained in capsules having cell wall comprised of said Arabic gum and gelatin of about 9.0 weight percent;
(v) admitting said capsular adhesive blend to said operating dry mixer in a weight percent range from about 6 to about 12 weight percent of said signal illuminant flare composition ingredients to achieve homogeneity;
(vi) feeding said homogeneously, blended signal illuminant flare composition into a flare increment feeder for incremental feeding the same into a flare press for compacting into paper cartridges;
(vii) compacting said blended signal illuminant flare composition into a paper cartridge in two increments while employing 14,000 psi pressure which ruptures said capsular adhesives by hydraulic forces to achieve polymer mixing and the surrounding of the powder ingredients with said binder ingredients to thereby form a very homogeneous signal illuminant flare composition mass; and
(viii) curing said homogeneous signal illuminant flare composition mass for about 16 hours at a maximum temperature of about 170° F. to yield said signal illuminant flare.
2. The signal illuminant flare manufactured by the method of claim 1 wherein said flare has a density in grams per cubic centimeter, a burning rate in inches per second, and a candlepower which varies in a accordance with said binder weight percent and said magnesium weight percent as set forth below for said signal illuminant flare composition having mix numbers 1-4 as follows:
______________________________________ Mix Density Burning No. Binder % Mg (%) (gm/cc) Rate (ips) Candlepower ______________________________________ 1 6 45 1.808 0.0640 137,400 2 6 50 1.762 0.0799 173.300 3 6 55 1.707 0.0996 202.400 4 6 57 1.686 0.1119 201,400 5 8 45 1.847 0.0748 151,100 6 8 50 1.794 0.0748 151,100 8 8 60 1.696 0.1110 161,700 9 10 45 1.858 0.0580 101,800 10 10 50 1.815 0.0730 119,500 11 10 55 1.764 0.0870 130,900 12 10 60 1.728 0.0996 126,600 13 12 50 1.863 0.0548 115.100 14 12 55 1.787 0.0752 103,800 ______________________________________
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US07/440,065 USH925H (en) | 1989-11-22 | 1989-11-22 | Encapsulated signal illumination flare composition |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US07/440,065 USH925H (en) | 1989-11-22 | 1989-11-22 | Encapsulated signal illumination flare composition |
Publications (1)
Publication Number | Publication Date |
---|---|
USH925H true USH925H (en) | 1991-06-04 |
Family
ID=23747272
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US07/440,065 Abandoned USH925H (en) | 1989-11-22 | 1989-11-22 | Encapsulated signal illumination flare composition |
Country Status (1)
Country | Link |
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US (1) | USH925H (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US20160273897A1 (en) * | 2013-03-12 | 2016-09-22 | Wendell Diller | Shotgun Shell Tracer and Tracer Manufacturing Device |
US10155700B2 (en) | 2011-11-04 | 2018-12-18 | Northrop Grumman Innovation Systems, Inc. | Consumable weight components for flares and methods of formation |
-
1989
- 1989-11-22 US US07/440,065 patent/USH925H/en not_active Abandoned
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US10155700B2 (en) | 2011-11-04 | 2018-12-18 | Northrop Grumman Innovation Systems, Inc. | Consumable weight components for flares and methods of formation |
US10647620B2 (en) | 2011-11-04 | 2020-05-12 | Northrop Grumman Innovation Systems, Inc. | Consumable weight components for flares and related flares |
US20160273897A1 (en) * | 2013-03-12 | 2016-09-22 | Wendell Diller | Shotgun Shell Tracer and Tracer Manufacturing Device |
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Owner name: UNITED STATES OF AMERICA, THE, AS REPRESENTED BY T Free format text: ASSIGNMENT OF ASSIGNORS INTEREST.;ASSIGNOR:SAYLES, DAVID C.;REEL/FRAME:005637/0372 Effective date: 19891025 |
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STCF | Information on status: patent grant |
Free format text: PATENTED CASE |