SE444808B - Herdbart bindemedel, for anvendning vid framstellning av ett gjutbart drivmedel, baserat pa en butadienpolymer med hydroxyl i endstellning - Google Patents

Herdbart bindemedel, for anvendning vid framstellning av ett gjutbart drivmedel, baserat pa en butadienpolymer med hydroxyl i endstellning

Info

Publication number: SE444808B
Authority: SE; Sweden
Prior art keywords: binder; weight; amount; polyester; antioxidant
Prior art date: 1977-12-13

Application number

SE7812668A

Other languages

English (en)

Swedish (sv)

Other versions

SE7812668L (sv

Inventor

G L Duchesne

G Perrault

Original Assignee

Ca Minister Nat Defence

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.)

1977-12-13

Filing date

1978-12-08

Publication date

1986-05-12

1977-12-13 Priority claimed from CA292,954A external-priority patent/CA1086955A/en

1978-12-08 Application filed by Ca Minister Nat Defence filed Critical Ca Minister Nat Defence

1979-06-14 Publication of SE7812668L publication Critical patent/SE7812668L/xx

1986-05-12 Publication of SE444808B publication Critical patent/SE444808B/sv

Links

239000011230 binding agent Substances 0.000 title claims description 76
239000000446 fuel Substances 0.000 title description 50
238000002360 preparation method Methods 0.000 title description 8
229920002587 poly(1,3-butadiene) polymer Polymers 0.000 title description 3
TUJKJAMUKRIRHC-UHFFFAOYSA-N hydroxyl Chemical class [OH] TUJKJAMUKRIRHC-UHFFFAOYSA-N 0.000 title 1
239000000203 mixture Substances 0.000 claims description 96
239000003963 antioxidant agent Substances 0.000 claims description 62
JZODKRWQWUWGCD-UHFFFAOYSA-N 2,5-di-tert-butylbenzene-1,4-diol Chemical compound CC(C)(C)C1=CC(O)=C(C(C)(C)C)C=C1O JZODKRWQWUWGCD-UHFFFAOYSA-N 0.000 claims description 47
239000003380 propellant Substances 0.000 claims description 45
230000003078 antioxidant effect Effects 0.000 claims description 35
229920000728 polyester Polymers 0.000 claims description 34
NOWKCMXCCJGMRR-UHFFFAOYSA-N Aziridine Chemical compound C1CN1 NOWKCMXCCJGMRR-UHFFFAOYSA-N 0.000 claims description 24
239000007795 chemical reaction product Substances 0.000 claims description 16
150000001412 amines Chemical class 0.000 claims description 13
229920000642 polymer Polymers 0.000 claims description 13
239000002253 acid Substances 0.000 claims description 12
125000005442 diisocyanate group Chemical group 0.000 claims description 11
239000004014 plasticizer Substances 0.000 claims description 10
239000004848 polyfunctional curative Substances 0.000 claims description 10
125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims description 9
239000002131 composite material Substances 0.000 claims description 7
229920002857 polybutadiene Polymers 0.000 claims description 7
WYFRCNZIOOYQHH-UHFFFAOYSA-N N1(CC1)[PH2]=O Chemical compound N1(CC1)[PH2]=O WYFRCNZIOOYQHH-UHFFFAOYSA-N 0.000 claims description 6
WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 claims description 6
CXMXRPHRNRROMY-UHFFFAOYSA-N sebacic acid Chemical compound OC(=O)CCCCCCCCC(O)=O CXMXRPHRNRROMY-UHFFFAOYSA-N 0.000 claims description 6
239000005062 Polybutadiene Substances 0.000 claims description 5
125000001931 aliphatic group Chemical group 0.000 claims description 5
229910052739 hydrogen Inorganic materials 0.000 claims description 4
238000004519 manufacturing process Methods 0.000 claims description 4
FEWJPZIEWOKRBE-JCYAYHJZSA-N Dextrotartaric acid Chemical compound OC(=O)[C@H](O)[C@@H](O)C(O)=O FEWJPZIEWOKRBE-JCYAYHJZSA-N 0.000 claims description 3
239000001361 adipic acid Substances 0.000 claims description 3
235000011037 adipic acid Nutrition 0.000 claims description 3
-1 diethyl butylhydroquinone Chemical compound 0.000 claims description 3
ZZMVLMVFYMGSMY-UHFFFAOYSA-N 4-n-(4-methylpentan-2-yl)-1-n-phenylbenzene-1,4-diamine Chemical compound C1=CC(NC(C)CC(C)C)=CC=C1NC1=CC=CC=C1 ZZMVLMVFYMGSMY-UHFFFAOYSA-N 0.000 claims description 2
GBLPOPTXAXWWPO-UHFFFAOYSA-N 8-methylnonyl nonanoate Chemical compound CCCCCCCCC(=O)OCCCCCCCC(C)C GBLPOPTXAXWWPO-UHFFFAOYSA-N 0.000 claims description 2
229960001270 d- tartaric acid Drugs 0.000 claims description 2
CRVGTESFCCXCTH-UHFFFAOYSA-N methyl diethanolamine Chemical compound OCCN(C)CCO CRVGTESFCCXCTH-UHFFFAOYSA-N 0.000 claims description 2
AUONHKJOIZSQGR-UHFFFAOYSA-N oxophosphane Chemical compound P=O AUONHKJOIZSQGR-UHFFFAOYSA-N 0.000 claims description 2
VJIDDJAKLVOBSE-UHFFFAOYSA-N 2-ethylbenzene-1,4-diol Chemical compound CCC1=CC(O)=CC=C1O VJIDDJAKLVOBSE-UHFFFAOYSA-N 0.000 claims 2
MDDUHVRJJAFRAU-YZNNVMRBSA-N tert-butyl-[(1r,3s,5z)-3-[tert-butyl(dimethyl)silyl]oxy-5-(2-diphenylphosphorylethylidene)-4-methylidenecyclohexyl]oxy-dimethylsilane Chemical compound C1[C@@H](O[Si](C)(C)C(C)(C)C)C[C@H](O[Si](C)(C)C(C)(C)C)C(=C)\C1=C/CP(=O)(C=1C=CC=CC=1)C1=CC=CC=C1 MDDUHVRJJAFRAU-YZNNVMRBSA-N 0.000 claims 1
125000000383 tetramethylene group Chemical group [H]C([H])([*:1])C([H])([H])C([H])([H])C([H])([H])[*:2] 0.000 claims 1
230000032683 aging Effects 0.000 description 16
230000000694 effects Effects 0.000 description 16
GDDNTTHUKVNJRA-UHFFFAOYSA-N 3-bromo-3,3-difluoroprop-1-ene Chemical compound FC(F)(Br)C=C GDDNTTHUKVNJRA-UHFFFAOYSA-N 0.000 description 14
229920002121 Hydroxyl-terminated polybutadiene Polymers 0.000 description 14
125000002887 hydroxy group Chemical group [H]O* 0.000 description 14
238000002156 mixing Methods 0.000 description 13
KEQFTVQCIQJIQW-UHFFFAOYSA-N N-Phenyl-2-naphthylamine Chemical compound C=1C=C2C=CC=CC2=CC=1NC1=CC=CC=C1 KEQFTVQCIQJIQW-UHFFFAOYSA-N 0.000 description 11
239000007787 solid Substances 0.000 description 8
239000007800 oxidant agent Substances 0.000 description 7
238000012545 processing Methods 0.000 description 7
125000000217 alkyl group Chemical group 0.000 description 6
150000001875 compounds Chemical class 0.000 description 6
238000000034 method Methods 0.000 description 6
239000002245 particle Substances 0.000 description 6
AVUYXHYHTTVPRX-UHFFFAOYSA-N Tris(2-methyl-1-aziridinyl)phosphine oxide Chemical compound CC1CN1P(=O)(N1C(C1)C)N1C(C)C1 AVUYXHYHTTVPRX-UHFFFAOYSA-N 0.000 description 5
125000004432 carbon atom Chemical group C* 0.000 description 5
239000003795 chemical substances by application Substances 0.000 description 5
238000005259 measurement Methods 0.000 description 5
UQSXHKLRYXJYBZ-UHFFFAOYSA-N Iron oxide Chemical compound [Fe]=O UQSXHKLRYXJYBZ-UHFFFAOYSA-N 0.000 description 4
239000000654 additive Substances 0.000 description 4
230000000996 additive effect Effects 0.000 description 4
XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 4
239000003054 catalyst Substances 0.000 description 4
238000010586 diagram Methods 0.000 description 4
239000000463 material Substances 0.000 description 4
MVAOEXBRERPGIT-UHFFFAOYSA-N octamine Chemical compound N.N.N.N.N.N.N.N MVAOEXBRERPGIT-UHFFFAOYSA-N 0.000 description 4
239000000047 product Substances 0.000 description 4
238000012360 testing method Methods 0.000 description 4
239000004593 Epoxy Substances 0.000 description 3
OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 3
229910052782 aluminium Inorganic materials 0.000 description 3
238000005266 casting Methods 0.000 description 3
238000002485 combustion reaction Methods 0.000 description 3
150000001991 dicarboxylic acids Chemical class 0.000 description 3
238000010438 heat treatment Methods 0.000 description 3
239000001257 hydrogen Substances 0.000 description 3
239000007788 liquid Substances 0.000 description 3
230000003647 oxidation Effects 0.000 description 3
238000007254 oxidation reaction Methods 0.000 description 3
238000011417 postcuring Methods 0.000 description 3
239000000126 substance Substances 0.000 description 3
229930185605 Bisphenol Natural products 0.000 description 2
241000566113 Branta sandvicensis Species 0.000 description 2
KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical compound C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 description 2
XZMCDFZZKTWFGF-UHFFFAOYSA-N Cyanamide Chemical compound NC#N XZMCDFZZKTWFGF-UHFFFAOYSA-N 0.000 description 2
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 2
ZFMQKOWCDKKBIF-UHFFFAOYSA-N bis(3,5-difluorophenyl)phosphane Chemical compound FC1=CC(F)=CC(PC=2C=C(F)C=C(F)C=2)=C1 ZFMQKOWCDKKBIF-UHFFFAOYSA-N 0.000 description 2
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 description 2
238000006243 chemical reaction Methods 0.000 description 2
230000006866 deterioration Effects 0.000 description 2
239000006185 dispersion Substances 0.000 description 2
238000009826 distribution Methods 0.000 description 2
150000002148 esters Chemical class 0.000 description 2
RRAMGCGOFNQTLD-UHFFFAOYSA-N hexamethylene diisocyanate Chemical compound O=C=NCCCCCCN=C=O RRAMGCGOFNQTLD-UHFFFAOYSA-N 0.000 description 2
125000004435 hydrogen atom Chemical group [H]* 0.000 description 2
239000012948 isocyanate Substances 0.000 description 2
150000002513 isocyanates Chemical class 0.000 description 2
229910052751 metal Inorganic materials 0.000 description 2
239000002184 metal Substances 0.000 description 2
NDLPOXTZKUMGOV-UHFFFAOYSA-N oxo(oxoferriooxy)iron hydrate Chemical group O.O=[Fe]O[Fe]=O NDLPOXTZKUMGOV-UHFFFAOYSA-N 0.000 description 2
239000000843 powder Substances 0.000 description 2
230000001105 regulatory effect Effects 0.000 description 2
KDYFGRWQOYBRFD-UHFFFAOYSA-N succinic acid Chemical compound OC(=O)CCC(O)=O KDYFGRWQOYBRFD-UHFFFAOYSA-N 0.000 description 2
230000002195 synergetic effect Effects 0.000 description 2
MHCVCKDNQYMGEX-UHFFFAOYSA-N 1,1'-biphenyl;phenoxybenzene Chemical group C1=CC=CC=C1C1=CC=CC=C1.C=1C=CC=CC=1OC1=CC=CC=C1 MHCVCKDNQYMGEX-UHFFFAOYSA-N 0.000 description 1
RBACIKXCRWGCBB-UHFFFAOYSA-N 1,2-Epoxybutane Chemical compound CCC1CO1 RBACIKXCRWGCBB-UHFFFAOYSA-N 0.000 description 1
CBCKQZAAMUWICA-UHFFFAOYSA-N 1,4-phenylenediamine Chemical compound NC1=CC=C(N)C=C1 CBCKQZAAMUWICA-UHFFFAOYSA-N 0.000 description 1
229940008841 1,6-hexamethylene diisocyanate Drugs 0.000 description 1
DMYOHQBLOZMDLP-UHFFFAOYSA-N 1-[2-(2-hydroxy-3-piperidin-1-ylpropoxy)phenyl]-3-phenylpropan-1-one Chemical compound C1CCCCN1CC(O)COC1=CC=CC=C1C(=O)CCC1=CC=CC=C1 DMYOHQBLOZMDLP-UHFFFAOYSA-N 0.000 description 1
ZRMMVODKVLXCBB-UHFFFAOYSA-N 1-n-cyclohexyl-4-n-phenylbenzene-1,4-diamine Chemical compound C1CCCCC1NC(C=C1)=CC=C1NC1=CC=CC=C1 ZRMMVODKVLXCBB-UHFFFAOYSA-N 0.000 description 1
ZNRLMGFXSPUZNR-UHFFFAOYSA-N 2,2,4-trimethyl-1h-quinoline Chemical compound C1=CC=C2C(C)=CC(C)(C)NC2=C1 ZNRLMGFXSPUZNR-UHFFFAOYSA-N 0.000 description 1
XRCRJFOGPCJKPF-UHFFFAOYSA-N 2-butylbenzene-1,4-diol Chemical compound CCCCC1=CC(O)=CC=C1O XRCRJFOGPCJKPF-UHFFFAOYSA-N 0.000 description 1
FESXASKNNCELJT-UHFFFAOYSA-N 2-methylprop-1-ene;n-phenylaniline Chemical group CC(C)=C.CC(C)=C.C=1C=CC=CC=1NC1=CC=CC=C1 FESXASKNNCELJT-UHFFFAOYSA-N 0.000 description 1
BBCLXYJRPRRZQW-UHFFFAOYSA-N 2-phenylnaphthalen-1-amine Chemical compound C1=CC2=CC=CC=C2C(N)=C1C1=CC=CC=C1 BBCLXYJRPRRZQW-UHFFFAOYSA-N 0.000 description 1
238000012935 Averaging Methods 0.000 description 1
FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 1
239000004698 Polyethylene Substances 0.000 description 1
GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 description 1
FEWJPZIEWOKRBE-UHFFFAOYSA-N Tartaric acid Natural products [H+].[H+].[O-]C(=O)C(O)C(O)C([O-])=O FEWJPZIEWOKRBE-UHFFFAOYSA-N 0.000 description 1
229920001079 Thiokol (polymer) Polymers 0.000 description 1
239000007983 Tris buffer Substances 0.000 description 1
230000003679 aging effect Effects 0.000 description 1
AZDRQVAHHNSJOQ-UHFFFAOYSA-N alumane Chemical compound [AlH3] AZDRQVAHHNSJOQ-UHFFFAOYSA-N 0.000 description 1
125000003118 aryl group Chemical group 0.000 description 1
230000009286 beneficial effect Effects 0.000 description 1
125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 description 1
230000015572 biosynthetic process Effects 0.000 description 1
210000000988 bone and bone Anatomy 0.000 description 1
239000001506 calcium phosphate Substances 0.000 description 1
239000003183 carcinogenic agent Substances 0.000 description 1
125000003636 chemical group Chemical group 0.000 description 1
230000000052 comparative effect Effects 0.000 description 1
239000007859 condensation product Substances 0.000 description 1
JGDFBJMWFLXCLJ-UHFFFAOYSA-N copper chromite Chemical compound [Cu]=O.[Cu]=O.O=[Cr]O[Cr]=O JGDFBJMWFLXCLJ-UHFFFAOYSA-N 0.000 description 1
230000001419 dependent effect Effects 0.000 description 1
150000004985 diamines Chemical class 0.000 description 1
235000014113 dietary fatty acids Nutrition 0.000 description 1
238000006471 dimerization reaction Methods 0.000 description 1
AXZAYXJCENRGIM-UHFFFAOYSA-J dipotassium;tetrabromoplatinum(2-) Chemical compound [K+].[K+].[Br-].[Br-].[Br-].[Br-].[Pt+2] AXZAYXJCENRGIM-UHFFFAOYSA-J 0.000 description 1
125000003700 epoxy group Chemical group 0.000 description 1
239000003822 epoxy resin Substances 0.000 description 1
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
238000011156 evaluation Methods 0.000 description 1
238000002474 experimental method Methods 0.000 description 1
239000000194 fatty acid Substances 0.000 description 1
229930195729 fatty acid Natural products 0.000 description 1
150000004665 fatty acids Chemical class 0.000 description 1
AOGQPLXWSUTHQB-UHFFFAOYSA-N hexyl acetic acid ester Natural products CCCCCCOC(C)=O AOGQPLXWSUTHQB-UHFFFAOYSA-N 0.000 description 1
238000010348 incorporation Methods 0.000 description 1
239000004615 ingredient Substances 0.000 description 1
LIKBJVNGSGBSGK-UHFFFAOYSA-N iron(3+);oxygen(2-) Chemical compound [O-2].[O-2].[O-2].[Fe+3].[Fe+3] LIKBJVNGSGBSGK-UHFFFAOYSA-N 0.000 description 1
JEIPFZHSYJVQDO-UHFFFAOYSA-N iron(III) oxide Inorganic materials O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 0.000 description 1
238000009533 lab test Methods 0.000 description 1
VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 1
239000011976 maleic acid Substances 0.000 description 1
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
SYSQUGFVNFXIIT-UHFFFAOYSA-N n-[4-(1,3-benzoxazol-2-yl)phenyl]-4-nitrobenzenesulfonamide Chemical class C1=CC([N+](=O)[O-])=CC=C1S(=O)(=O)NC1=CC=C(C=2OC3=CC=CC=C3N=2)C=C1 SYSQUGFVNFXIIT-UHFFFAOYSA-N 0.000 description 1
FBUKVWPVBMHYJY-UHFFFAOYSA-M nonanoate Chemical compound CCCCCCCCC([O-])=O FBUKVWPVBMHYJY-UHFFFAOYSA-M 0.000 description 1
150000002894 organic compounds Chemical class 0.000 description 1
150000002902 organometallic compounds Chemical class 0.000 description 1
230000001590 oxidative effect Effects 0.000 description 1
150000004989 p-phenylenediamines Chemical class 0.000 description 1
VLTRZXGMWDSKGL-UHFFFAOYSA-M perchlorate Inorganic materials [O-]Cl(=O)(=O)=O VLTRZXGMWDSKGL-UHFFFAOYSA-M 0.000 description 1
VLTRZXGMWDSKGL-UHFFFAOYSA-N perchloric acid Chemical compound OCl(=O)(=O)=O VLTRZXGMWDSKGL-UHFFFAOYSA-N 0.000 description 1
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
229920000647 polyepoxide Polymers 0.000 description 1
229920000573 polyethylene Polymers 0.000 description 1
238000006116 polymerization reaction Methods 0.000 description 1
230000000379 polymerizing effect Effects 0.000 description 1
229910001487 potassium perchlorate Inorganic materials 0.000 description 1
239000002243 precursor Substances 0.000 description 1
239000000376 reactant Substances 0.000 description 1
239000000523 sample Substances 0.000 description 1
239000011343 solid material Substances 0.000 description 1
239000004449 solid propellant Substances 0.000 description 1
238000003756 stirring Methods 0.000 description 1
239000001384 succinic acid Substances 0.000 description 1
238000003786 synthesis reaction Methods 0.000 description 1
229960001367 tartaric acid Drugs 0.000 description 1
239000011975 tartaric acid Substances 0.000 description 1
235000002906 tartaric acid Nutrition 0.000 description 1
DVKJHBMWWAPEIU-UHFFFAOYSA-N toluene 2,4-diisocyanate Chemical compound CC1=CC=C(N=C=O)C=C1N=C=O DVKJHBMWWAPEIU-UHFFFAOYSA-N 0.000 description 1
VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 1
QORWJWZARLRLPR-UHFFFAOYSA-H tricalcium bis(phosphate) Chemical compound [Ca+2].[Ca+2].[Ca+2].[O-]P([O-])([O-])=O.[O-]P([O-])([O-])=O QORWJWZARLRLPR-UHFFFAOYSA-H 0.000 description 1
229940078499 tricalcium phosphate Drugs 0.000 description 1
229910000391 tricalcium phosphate Inorganic materials 0.000 description 1
235000019731 tricalcium phosphate Nutrition 0.000 description 1
125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
229920002554 vinyl polymer Polymers 0.000 description 1
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L75/00—Compositions of polyureas or polyurethanes; Compositions of derivatives of such polymers
- C08L75/04—Polyurethanes
- C08L75/14—Polyurethanes having carbon-to-carbon unsaturated bonds
- C—CHEMISTRY; METALLURGY
- C06—EXPLOSIVES; MATCHES
- C06B—EXPLOSIVES OR THERMIC COMPOSITIONS; MANUFACTURE THEREOF; USE OF SINGLE SUBSTANCES AS EXPLOSIVES
- C06B45/00—Compositions or products which are defined by structure or arrangement of component of product
- C06B45/04—Compositions or products which are defined by structure or arrangement of component of product comprising solid particles dispersed in solid solution or matrix not used for explosives where the matrix consists essentially of nitrated carbohydrates or a low molecular organic explosive
- C06B45/06—Compositions or products which are defined by structure or arrangement of component of product comprising solid particles dispersed in solid solution or matrix not used for explosives where the matrix consists essentially of nitrated carbohydrates or a low molecular organic explosive the solid solution or matrix containing an organic component
- C06B45/10—Compositions or products which are defined by structure or arrangement of component of product comprising solid particles dispersed in solid solution or matrix not used for explosives where the matrix consists essentially of nitrated carbohydrates or a low molecular organic explosive the solid solution or matrix containing an organic component the organic component containing a resin
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
- C08G18/40—High-molecular-weight compounds
- C08G18/42—Polycondensates having carboxylic or carbonic ester groups in the main chain
- C08G18/46—Polycondensates having carboxylic or carbonic ester groups in the main chain having heteroatoms other than oxygen
- C08G18/4615—Polycondensates having carboxylic or carbonic ester groups in the main chain having heteroatoms other than oxygen containing nitrogen
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
- C08G18/67—Unsaturated compounds having active hydrogen
- C08G18/69—Polymers of conjugated dienes
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L67/00—Compositions of polyesters obtained by reactions forming a carboxylic ester link in the main chain; Compositions of derivatives of such polymers
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D161/00—Coating compositions based on condensation polymers of aldehydes or ketones; Coating compositions based on derivatives of such polymers
- C09D161/04—Condensation polymers of aldehydes or ketones with phenols only
- C09D161/06—Condensation polymers of aldehydes or ketones with phenols only of aldehydes with phenols

Landscapes

Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
Health & Medical Sciences (AREA)
Chemical Kinetics & Catalysis (AREA)
Medicinal Chemistry (AREA)
Polymers & Plastics (AREA)
Life Sciences & Earth Sciences (AREA)
Materials Engineering (AREA)
Engineering & Computer Science (AREA)
Wood Science & Technology (AREA)
Dispersion Chemistry (AREA)
Molecular Biology (AREA)
Crystallography & Structural Chemistry (AREA)
Compositions Of Macromolecular Compounds (AREA)
Polyurethanes Or Polyureas (AREA)
Adhesives Or Adhesive Processes (AREA)
Sealing Material Composition (AREA)

SE7812668A 1977-12-13 1978-12-08 Herdbart bindemedel, for anvendning vid framstellning av ett gjutbart drivmedel, baserat pa en butadienpolymer med hydroxyl i endstellning SE444808B (sv)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
CA292,954A CA1086955A (en)	1977-01-04	1977-12-13	Polyester bonding agents for htpb propellants

Publications (2)

Publication Number	Publication Date
SE7812668L SE7812668L (sv)	1979-06-14
SE444808B true SE444808B (sv)	1986-05-12

Family

ID=4110270

Family Applications (2)

Application Number	Title	Priority Date	Filing Date
SE7812668A SE444808B (sv)	1977-12-13	1978-12-08	Herdbart bindemedel, for anvendning vid framstellning av ett gjutbart drivmedel, baserat pa en butadienpolymer med hydroxyl i endstellning
SE8304823A SE451068B (sv)	1977-12-13	1983-09-08	Drivmedel av typen polybutadien med hydroxylgrupper i endstellning samt forfarande for dess framstellning

Family Applications After (1)

Application Number	Title	Priority Date	Filing Date
SE8304823A SE451068B (sv)	1977-12-13	1983-09-08	Drivmedel av typen polybutadien med hydroxylgrupper i endstellning samt forfarande for dess framstellning

Country Status (10)

Country	Link
JP (1)	JPS5484016A (da)
BE (1)	BE869617A (da)
DE (1)	DE2830495A1 (da)
DK (1)	DK539078A (da)
FR (1)	FR2411872A1 (da)
GB (1)	GB1604197A (da)
IT (1)	IT1106293B (da)
NL (1)	NL7812148A (da)
NO (1)	NO146492C (da)
SE (2)	SE444808B (da)

Families Citing this family (9)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US4352397A (en) *	1980-10-03	1982-10-05	Jet Research Center, Inc.	Methods, apparatus and pyrotechnic compositions for severing conduits
NO831850L (no) *	1982-05-28	1997-02-26	Royal Ordnance Plc	Fremgangsmåte for fremstilling av en formet gummiaktig drivmiddelladning for raketter og liknende
JPS5973489A (ja) *	1982-10-20	1984-04-25	日本油脂株式会社	固体推進薬用の粘結剤
JPS5973488A (ja) *	1982-10-20	1984-04-25	日本油脂株式会社	固体推進薬用粘結剤
EP0266973A3 (en) *	1986-11-06	1990-01-10	Thiokol Corporation	Pcp/htpb block copolymer and propellant binder prepared therefrom
FR3051188B1 (fr) *	2016-05-12	2022-04-22	Herakles	Explosif composite a vitesse de detonation lente et generateur d'onde plane ou lineaire en renfermant
JP7775574B2 (ja) *	2021-03-31	2025-11-26	日油株式会社	コンポジット推進薬
CN114591363B (zh) *	2022-02-28	2024-01-23	武汉理工大学	一种多官能度支化磷酸酰胺键合剂、其制备方法及复合固体推进剂
CN115746766A (zh) *	2022-11-25	2023-03-07	天元航材(营口)科技股份有限公司	一种环氧橡胶胶粘剂及其制备方法和应用

Family Cites Families (2)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
CA243659A (en) *		1924-10-14	Frans Wilhelmi Dirk	Rubber sole
CA1056984A (en) *	1976-01-16	1979-06-19	Her Majesty The Queen In Right Of Canada As Represented By The Minister Of National Defence Of Her Majesty's Canadian Government	Curable binding systems

1978
- 1978-05-16 GB GB19718/78A patent/GB1604197A/en not_active Expired
- 1978-07-11 DE DE19782830495 patent/DE2830495A1/de not_active Withdrawn
- 1978-07-31 FR FR7822599A patent/FR2411872A1/fr active Granted
- 1978-08-08 BE BE189782A patent/BE869617A/xx not_active IP Right Cessation
- 1978-08-31 IT IT50927/78A patent/IT1106293B/it active
- 1978-10-04 JP JP12249878A patent/JPS5484016A/ja active Pending
- 1978-10-13 NO NO783480A patent/NO146492C/no unknown
- 1978-11-30 DK DK539078A patent/DK539078A/da not_active Application Discontinuation
- 1978-12-08 SE SE7812668A patent/SE444808B/sv unknown
- 1978-12-13 NL NL7812148A patent/NL7812148A/xx not_active Application Discontinuation
1983
- 1983-09-08 SE SE8304823A patent/SE451068B/sv unknown

Also Published As

Publication number	Publication date
FR2411872A1 (fr)	1979-07-13
DE2830495A1 (de)	1979-06-21
IT7850927A0 (it)	1978-08-31
SE451068B (sv)	1987-08-31
SE7812668L (sv)	1979-06-14
FR2411872B1 (da)	1983-10-07
BE869617A (fr)	1978-12-01
NO146492C (no)	1982-10-13
GB1604197A (en)	1981-12-02
NL7812148A (nl)	1979-06-15
JPS5484016A (en)	1979-07-04
IT1106293B (it)	1985-11-11
NO783480L (no)	1979-06-14
SE8304823L (sv)	1983-09-08
DK539078A (da)	1979-07-06
NO146492B (no)	1982-07-05
SE8304823D0 (sv)	1983-09-08

Legal Events

Date

Code

Title

Description

1995-01-31

NAL

Patent in force

Ref document number: 7812668-7

Format of ref document f/p: F

Publication	Publication Date	Title
SE444808B (sv)	1986-05-12	Herdbart bindemedel, for anvendning vid framstellning av ett gjutbart drivmedel, baserat pa en butadienpolymer med hydroxyl i endstellning
JP4999228B2 (ja)	2012-08-15	押出可能な熱可塑性エラストマー性尿素鎖延長ポリウレタン
CN109952333B (zh)	2022-04-05	聚碳化二亚胺共聚物
US4427468A (en)	1984-01-24	Curable propellant binding systems with bonding agent combination
JP2002532292A5 (da)	2007-02-08
US4090893A (en)	1978-05-23	Bonding agent system for improved propellant aging and low temperature physical properties
US4517035A (en)	1985-05-14	Method of making a castable propellant
CA1056984A (en)	1979-06-19	Curable binding systems
KR101101218B1 (ko)	2012-01-04	기계적 특성이 우수한 ｇａｐ/니트라민계 고에너지 추진제 조성물
US4412875A (en)	1983-11-01	Nitramine composite propellant compostion
EP0523709A1 (en)	1993-01-20	Polyurethane composition
CA1086955A (en)	1980-10-07	Polyester bonding agents for htpb propellants
JP7291609B2 (ja)	2023-06-15	熱可塑性ポリウレタンエラストマー組成物
US3715246A (en)	1973-02-06	Propellants derived from crosslinking of polybutadiene elastomers
Kohga et al.	2013	Viscoelastic and thermal decomposition behaviors of polytetrahydrofuran binder prepared using glycerin as a crosslinking modifier
JP2014101502A (ja)	2014-06-05	ポリアミドイミド樹脂組成物
FR2489815A1 (fr)	1982-03-12	Liant pour propergols reticules a simple ou double base
JP2012219107A (ja)	2012-11-12	ポリアミドイミド樹脂組成物、その製造法、それを用いた硬化性樹脂組成物及び塗料
Smith et al.	1971	HTPB propellants for large booster applications
US3252819A (en)	1966-05-24	N-vinyl amides and lactams as plasticizers for polyurethane potting and adhesive compositions
EP0096700B1 (en)	1985-08-07	Method for extension of pot life in curing reactions
JP3548585B2 (ja)	2004-07-28	爆薬組成物
JPH0425565A (ja)	1992-01-29	樹脂組成物
UST908011I4 (en)	1973-03-27	Defensive publication
WO2025186093A1 (en)	2025-09-12	Star-shaped polymers