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US4156700A Expired / Lapsed US ⏱️ 0.0 years remaining

Solid propellants containing polyether or polyester binders

Assignee: Department of National Defence
•
Filing: 1976-07-21
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Granted: 1979-05-29
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Expires: 1996-07-21
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Abstract

Abstract Useful hydroxyl-terminated polyolefin prepolymers, e.g. polybutadiene prepolymers, are provided which may be cross-linked with an epoxide to yield a polyether elastomeric material or with a mixture of an anhydride and an epoxide to form a polyester material. One such prepolymer is a carboxyl-terminated polyolefin, e.g. polybutadiene prepared by reacting a hydroxy-terminated polyolefin, e.g. polybutadiene with solid or liquid anhydrides. Polyether and polyester propellants containing up to about 88% of solid ammonium perchlorate in the powder form and aluminum powder may be prepared from the above two materials (binders). The physical and mechanical properties from these propellants depend on the ratios and on the order of addition of each ingredient, the curing temperature and the presence of surface-active agents. Polyester propellants may be made either by using the hydroxy-terminated polyolefin, e.g. polybutadiene prereacted with anhydrides or by mixing simultaneously all ingredients with the solids. Polyester propellants made by the former procedure have superior properties to those made from the latter. Polyether propellants have slightly lower mechanical and physical properties than those of polyesters. These properties are strongly dependent on the catalytic activity of ammonium perchlorate.

Inventors

  • 👤 Meude Tremblay
  • 👤 Guy Perrault
  • 👤 Gonzague Duchesne

Bibliographic Details

Application Number —
Jurisdiction US
Data Source google_patents
Last Synchronized 2026-11-07 12:24
CPC Classifications
C; C08; C08F; C08F8/00; C08F8/02; C06; C06B; C06B21/00; C06B21/0008; C06B21/0025; C06B45/00; C06B45/04; C06B45/06; C06B45/10; C08C; C08C19/00; C08C19/30; C08C19/34; C08L; C08L63/00

Claims Analysis

Total Claims: 13
Claim 1
Independent Claim 85 words
A process for preparing a cross-linked elastomer which comprises: (A) preparing a carboxyl-terminated polyolefin by reacting a hydroxyl-terminated polyolefin selected from the group consisting of polypentadiene, polyheptadiene and polyisoprene, each having hydroxyl end groups, and polyethylene, polybutylene, and polypropylene, each having hydroxyl end groups, with an acid anhydride; and (B) reacting the carboxyl derivative so formed with an epoxide containing at least two epoxide groups in the presence of a metallic salt catalyst selected from the group consisting of the monocarboxylic acid salts of chromium.
Claim 2
Dependent Claim 85 words
A process for preparing a cross-linked elastomer which comprises: (A) preparing a carboxyl-terminated polyolefin by reacting a hydroxyl-terminated polyolefin selected from the group consisting of polypentadiene, polyheptadiene and polyisoprene, each having hydroxyl end groups, and polyethylene, polybutylene, and polypropylene, each having hydroxyl end groups, with an acid anhydride; and (B) reacting the carboxyl derivative so formed with an epoxide containing at least two epoxide groups in the presence of a metallic salt catalyst selected from the group consisting of the monocarboxylic acid salts of chromium.
Claim 3
Dependent Claim 33 words
The process of claim 1 wherein, in step (A), the reaction is carried out in a solvent selected from the group consisting of benzene, toluene, methyl and ethyl acetate, dioxane, hexane and cyclohexane.
Claim 4
Dependent Claim 40 words
The process of claim 1 wherein, in step (A), the acid anhydride is selected from the group consisting of succinic anhydride, methylsuccinic anhydride, benzene dicarboxylic anhydride, phthallic anhydride, cyclobutanedicarboxylic anhydride, 3-methylglutaric anhydride, hexahydro-4-methylphthallic anhydride, 3-methylglutaric anhydride and cis-1,2 cyclohexane-dicarboxylic anhydride.
Claim 5
Dependent Claim 26 words
The process of claim 1 wherein said carboxyl-terminated polyolefin comprises carboxyl-terminated polybutadienes, which have been prepared by reacting hydroxyl-terminated polybutadienes with solid or liquid acid anhydrides.
Claim 6
Dependent Claim 18 words
The process of claim 4 wherein, in step (A), the reaction is carried out in benzene or toluene.
Claim 7
Dependent Claim 15 words
The process of claim 4 wherein, in step (A), the acid anhydride is cis-1,2-cyclohexanedicarboxylic acid.
Claim 8
Dependent Claim 37 words
The process of claim 1 wherein, in step (B), the metallic catalyst is selected from the group consisting of chromium diisopropyl salicylate, chromium naphthenate, chromium stearate, chromium acetylacetonate, chromium acetate, chromium oleate, chromium octanoate and chromium octoate.
Claim 9
Dependent Claim 23 words
The process of claim 4 wherein the metallic salt is selected from the group consisting of chromium oleate, chromium octanoate and chromium octoate.
Claim 10
Dependent Claim 51 words
The process of claim 1 wherein, in step (B), the epoxide is selected from the group consisting of: a diglycidyl ether of polyoxypropylene glycol; an epoxide derivative of triglycidyl glycerol; 3,4-epoxycyclohexymethyl-3',4'-epoxycyclohexane carboxylate; bis(3,4-epoxy-6-methylcyclohexylmethyl) adipate; N,N-diglycidyl-p-aminophenyl glycidyl ether; the epoxy derivative of sebacic acid, and the condensation product of epichlorohydrin and bisphenol-A.
Claim 11
Dependent Claim 51 words
The process of claim 4 wherein, in step (B), the epoxide is selected from the group consisting of: a diglycidyl ether of polyoxypropylene glycol; an epoxy derivative of triglycidyl glycerol; 3,4-epoxycyclohexylmethyl-3',4'-epoxycyclohexane carboxylate; bis(3,4-epoxy-6-methylcyclohexylmethyl) adipate; N,N-diglycidyl-p-aminophenyl glycidyl ether; the epoxy derivative of sebacic acid, and the condensation product of epichlorohydrin and bisphenol-A.
Claim 12
Dependent Claim 19 words
The process of claim 4 wherein, in step (B), the epoxide is a condensation product of epichlorohydrin and bisphenol-A.
Claim 13
Dependent Claim 17 words
The process of claim 4 wherein, in step (A) the anhydride is succinic anhydride or methylsuccinic anhydride.

References Cited (Backward Citations)

US3902935A Cited
US3427255A Cited
US3734786A Cited
US3975314A Cited

USPTO Annuity & Maintenance Windows

Annuity Stage Window Opens Payment Deadline Surcharge Period Until Estimated Fee Status
3.5 Years (Year 4) 1982-05-28 1982-11-27 1983-05-29 $2000.00 Window Closed / Lapsed
7.5 Years (Year 8) 1986-05-28 1986-11-27 1987-05-29 $3760.00 Window Closed / Lapsed
11.5 Years (Year 12) 1990-05-28 1990-11-27 1991-05-29 $7700.00 Window Closed / Lapsed

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