SE434752B - Herdbar komposition for anvendning vid framstellning av bundna polyuretandrivbrenslekorn - Google Patents

Herdbar komposition for anvendning vid framstellning av bundna polyuretandrivbrenslekorn

Info

Publication number: SE434752B
Authority: SE; Sweden
Prior art keywords: curable composition; diisocyanate; salicylate; divalent; composition according
Prior art date: 1976-11-15

Application number

SE7712842A

Other languages

English (en)

Swedish (sv)

Other versions

SE7712842L (sv

Inventor

W H Graham

I G Shepard

Original Assignee

Thiokol Corp

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.)

1976-11-15

Filing date

1977-11-14

Publication date

1984-08-13

1977-11-14 Application filed by Thiokol Corp filed Critical Thiokol Corp

1978-05-16 Publication of SE7712842L publication Critical patent/SE7712842L/xx

1984-08-13 Publication of SE434752B publication Critical patent/SE434752B/sv

Links

239000000203 mixture Substances 0.000 title claims description 23
239000004814 polyurethane Substances 0.000 title claims description 5
229920002635 polyurethane Polymers 0.000 title claims description 5
238000004519 manufacturing process Methods 0.000 title description 5
239000000446 fuel Substances 0.000 title description 4
-1 n-octyl Chemical group 0.000 claims description 28
125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 11
229920002857 polybutadiene Polymers 0.000 claims description 9
238000002360 preparation method Methods 0.000 claims description 9
239000005062 Polybutadiene Substances 0.000 claims description 7
150000001875 compounds Chemical class 0.000 claims description 7
229910052739 hydrogen Inorganic materials 0.000 claims description 7
239000001257 hydrogen Substances 0.000 claims description 7
125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 6
125000004432 carbon atom Chemical group C* 0.000 claims description 4
125000000217 alkyl group Chemical group 0.000 claims description 3
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 3
125000003118 aryl group Chemical group 0.000 claims description 2
125000002837 carbocyclic group Chemical group 0.000 claims description 2
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 2
125000000732 arylene group Chemical group 0.000 claims 1
125000004836 hexamethylene group Chemical group [H]C([H])([*:2])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[*:1] 0.000 claims 1
210000000056 organ Anatomy 0.000 claims 1
238000001723 curing Methods 0.000 description 23
239000012948 isocyanate Substances 0.000 description 18
239000003054 catalyst Substances 0.000 description 17
150000002513 isocyanates Chemical class 0.000 description 16
239000003380 propellant Substances 0.000 description 15
238000006243 chemical reaction Methods 0.000 description 11
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 11
239000000463 material Substances 0.000 description 9
102220566099 Antileukoproteinase_R45V_mutation Human genes 0.000 description 8
ISKQADXMHQSTHK-UHFFFAOYSA-N [4-(aminomethyl)phenyl]methanamine Chemical compound NCC1=CC=C(CN)C=C1 ISKQADXMHQSTHK-UHFFFAOYSA-N 0.000 description 8
229960001860 salicylate Drugs 0.000 description 8
101100298295 Drosophila melanogaster flfl gene Proteins 0.000 description 7
239000002981 blocking agent Substances 0.000 description 7
239000004848 polyfunctional curative Substances 0.000 description 7
239000005056 polyisocyanate Substances 0.000 description 6
229920001228 polyisocyanate Polymers 0.000 description 6
GETQZCLCWQTVFV-UHFFFAOYSA-N trimethylamine Chemical compound CN(C)C GETQZCLCWQTVFV-UHFFFAOYSA-N 0.000 description 6
JOYRKODLDBILNP-UHFFFAOYSA-N Ethyl urethane Chemical compound CCOC(N)=O JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 description 5
239000005057 Hexamethylene diisocyanate Substances 0.000 description 5
ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 5
125000005442 diisocyanate group Chemical group 0.000 description 5
IQPQWNKOIGAROB-UHFFFAOYSA-N isocyanate group Chemical group [N-]=C=O IQPQWNKOIGAROB-UHFFFAOYSA-N 0.000 description 5
238000000034 method Methods 0.000 description 5
238000012545 processing Methods 0.000 description 5
239000000047 product Substances 0.000 description 5
239000007787 solid Substances 0.000 description 5
GYCKQBWUSACYIF-UHFFFAOYSA-N Ethyl salicylate Chemical compound CCOC(=O)C1=CC=CC=C1O GYCKQBWUSACYIF-UHFFFAOYSA-N 0.000 description 4
ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 4
230000000903 blocking effect Effects 0.000 description 4
238000010494 dissociation reaction Methods 0.000 description 4
230000005593 dissociations Effects 0.000 description 4
229940005667 ethyl salicylate Drugs 0.000 description 4
RRAMGCGOFNQTLD-UHFFFAOYSA-N hexamethylene diisocyanate Chemical compound O=C=NCCCCCCN=C=O RRAMGCGOFNQTLD-UHFFFAOYSA-N 0.000 description 4
WCJLCOAEJIHPCW-UHFFFAOYSA-N octyl 2-hydroxybenzoate Chemical compound CCCCCCCCOC(=O)C1=CC=CC=C1O WCJLCOAEJIHPCW-UHFFFAOYSA-N 0.000 description 4
239000004014 plasticizer Substances 0.000 description 4
238000003860 storage Methods 0.000 description 4
YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 3
XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 3
YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
239000011230 binding agent Substances 0.000 description 3
LTPCXXMGKDQPAO-UHFFFAOYSA-L calcium;2-ethylhexanoate Chemical compound [Ca+2].CCCCC(CC)C([O-])=O.CCCCC(CC)C([O-])=O LTPCXXMGKDQPAO-UHFFFAOYSA-L 0.000 description 3
238000005266 casting Methods 0.000 description 3
238000002485 combustion reaction Methods 0.000 description 3
229920001971 elastomer Polymers 0.000 description 3
239000007788 liquid Substances 0.000 description 3
238000002156 mixing Methods 0.000 description 3
239000007800 oxidant agent Substances 0.000 description 3
239000005060 rubber Substances 0.000 description 3
150000003902 salicylic acid esters Chemical class 0.000 description 3
239000007858 starting material Substances 0.000 description 3
GDDNTTHUKVNJRA-UHFFFAOYSA-N 3-bromo-3,3-difluoroprop-1-ene Chemical compound FC(F)(Br)C=C GDDNTTHUKVNJRA-UHFFFAOYSA-N 0.000 description 2
KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical compound C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 description 2
UQSXHKLRYXJYBZ-UHFFFAOYSA-N Iron oxide Chemical compound [Fe]=O UQSXHKLRYXJYBZ-UHFFFAOYSA-N 0.000 description 2
OYHQOLUKZRVURQ-HZJYTTRNSA-N Linoleic acid Chemical compound CCCCC\C=C/C\C=C/CCCCCCCC(O)=O OYHQOLUKZRVURQ-HZJYTTRNSA-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
239000000470 constituent Substances 0.000 description 2
230000000694 effects Effects 0.000 description 2
238000005516 engineering process Methods 0.000 description 2
150000002148 esters Chemical class 0.000 description 2
229910052742 iron Inorganic materials 0.000 description 2
229910052751 metal Inorganic materials 0.000 description 2
239000002184 metal Chemical class 0.000 description 2
OOFYUBSXSJUOEF-UHFFFAOYSA-N octyl 2-hydroxy-3-methylbenzoate Chemical compound CCCCCCCCOC(=O)C1=CC=CC(C)=C1O OOFYUBSXSJUOEF-UHFFFAOYSA-N 0.000 description 2
150000002989 phenols Chemical class 0.000 description 2
150000003512 tertiary amines Chemical class 0.000 description 2
229940086542 triethylamine Drugs 0.000 description 2
150000003673 urethanes Chemical class 0.000 description 2
WFUDBPZFGCNRDM-UHFFFAOYSA-N 1-butylcyclopenta-1,3-diene;cyclopenta-1,3-diene;iron(2+) Chemical compound [Fe+2].C=1C=C[CH-]C=1.CCCCC1=CC=C[CH-]1 WFUDBPZFGCNRDM-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
UPMLOUAZCHDJJD-UHFFFAOYSA-N 4,4'-Diphenylmethane Diisocyanate Chemical compound C1=CC(N=C=O)=CC=C1CC1=CC=C(N=C=O)C=C1 UPMLOUAZCHDJJD-UHFFFAOYSA-N 0.000 description 1
OCKGFTQIICXDQW-ZEQRLZLVSA-N 5-[(1r)-1-hydroxy-2-[4-[(2r)-2-hydroxy-2-(4-methyl-1-oxo-3h-2-benzofuran-5-yl)ethyl]piperazin-1-yl]ethyl]-4-methyl-3h-2-benzofuran-1-one Chemical compound C1=C2C(=O)OCC2=C(C)C([C@@H](O)CN2CCN(CC2)C[C@H](O)C2=CC=C3C(=O)OCC3=C2C)=C1 OCKGFTQIICXDQW-ZEQRLZLVSA-N 0.000 description 1
JXSRRBVHLUJJFC-UHFFFAOYSA-N 7-amino-2-methylsulfanyl-[1,2,4]triazolo[1,5-a]pyrimidine-6-carbonitrile Chemical compound N1=CC(C#N)=C(N)N2N=C(SC)N=C21 JXSRRBVHLUJJFC-UHFFFAOYSA-N 0.000 description 1
ORILYTVJVMAKLC-UHFFFAOYSA-N Adamantane Natural products C1C(C2)CC3CC1CC2C3 ORILYTVJVMAKLC-UHFFFAOYSA-N 0.000 description 1
XWNRSWVPALQMQU-UHFFFAOYSA-N CC1=CC=C(N=C=O)C=C1N=C=O.CCCCCCCCOC(=O)C1=CC=CC(C)=C1O Chemical compound CC1=CC=C(N=C=O)C=C1N=C=O.CCCCCCCCOC(=O)C1=CC=CC(C)=C1O XWNRSWVPALQMQU-UHFFFAOYSA-N 0.000 description 1
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
239000005058 Isophorone diisocyanate Substances 0.000 description 1
229930194542 Keto Natural products 0.000 description 1
229920001730 Moisture cure polyurethane Polymers 0.000 description 1
239000006057 Non-nutritive feed additive Substances 0.000 description 1
239000000654 additive Substances 0.000 description 1
125000005907 alkyl ester group Chemical group 0.000 description 1
XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
239000000729 antidote Substances 0.000 description 1
229940075522 antidotes Drugs 0.000 description 1
238000013459 approach Methods 0.000 description 1
UHOVQNZJYSORNB-UHFFFAOYSA-N benzene Substances C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 1
239000007795 chemical reaction product Substances 0.000 description 1
239000003795 chemical substances by application Substances 0.000 description 1
238000001816 cooling Methods 0.000 description 1
229910052802 copper Inorganic materials 0.000 description 1
239000010949 copper Substances 0.000 description 1
229940075144 cylate Drugs 0.000 description 1
230000001419 dependent effect Effects 0.000 description 1
239000012975 dibutyltin dilaurate Substances 0.000 description 1
125000004772 dichloromethyl group Chemical group [H]C(Cl)(Cl)* 0.000 description 1
DROMNWUQASBTFM-UHFFFAOYSA-N dinonyl benzene-1,2-dicarboxylate Chemical compound CCCCCCCCCOC(=O)C1=CC=CC=C1C(=O)OCCCCCCCCC DROMNWUQASBTFM-UHFFFAOYSA-N 0.000 description 1
230000007613 environmental effect Effects 0.000 description 1
238000011049 filling Methods 0.000 description 1
230000009969 flowable effect Effects 0.000 description 1
238000010438 heat treatment Methods 0.000 description 1
JGPMMRGNQUBGND-UHFFFAOYSA-N idebenone Chemical compound COC1=C(OC)C(=O)C(CCCCCCCCCCO)=C(C)C1=O JGPMMRGNQUBGND-UHFFFAOYSA-N 0.000 description 1
230000001939 inductive effect Effects 0.000 description 1
LZKLAOYSENRNKR-LNTINUHCSA-N iron;(z)-4-oxoniumylidenepent-2-en-2-olate Chemical compound [Fe].C\C(O)=C\C(C)=O.C\C(O)=C\C(C)=O.C\C(O)=C\C(C)=O LZKLAOYSENRNKR-LNTINUHCSA-N 0.000 description 1
NIMLQBUJDJZYEJ-UHFFFAOYSA-N isophorone diisocyanate Chemical compound CC1(C)CC(N=C=O)CC(C)(CN=C=O)C1 NIMLQBUJDJZYEJ-UHFFFAOYSA-N 0.000 description 1
125000000468 ketone group Chemical group 0.000 description 1
238000011068 loading method Methods 0.000 description 1
238000013508 migration Methods 0.000 description 1
230000005012 migration Effects 0.000 description 1
GFDBQRBTMHJWCT-UHFFFAOYSA-N nonyl 3-ethyl-2-hydroxybenzoate Chemical compound CCCCCCCCCOC(=O)C1=CC=CC(CC)=C1O GFDBQRBTMHJWCT-UHFFFAOYSA-N 0.000 description 1
239000004033 plastic Substances 0.000 description 1
229920003023 plastic Polymers 0.000 description 1
229920000728 polyester Polymers 0.000 description 1
229920000570 polyether Polymers 0.000 description 1
229920000642 polymer Polymers 0.000 description 1
239000003755 preservative agent Substances 0.000 description 1
238000000746 purification Methods 0.000 description 1
239000000376 reactant Substances 0.000 description 1
230000009257 reactivity Effects 0.000 description 1
230000001105 regulatory effect Effects 0.000 description 1
150000003839 salts Chemical class 0.000 description 1
239000011343 solid material Substances 0.000 description 1
239000004449 solid propellant Substances 0.000 description 1
125000001424 substituent group Chemical group 0.000 description 1
239000004094 surface-active agent Substances 0.000 description 1
231100000331 toxic Toxicity 0.000 description 1
230000002588 toxic effect Effects 0.000 description 1
125000003866 trichloromethyl group Chemical group ClC(Cl)(Cl)* 0.000 description 1
230000007306 turnover Effects 0.000 description 1
238000013022 venting Methods 0.000 description 1

Classifications

- 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
- C08G18/70—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the isocyanates or isothiocyanates used
- C08G18/72—Polyisocyanates or polyisothiocyanates
- C08G18/80—Masked polyisocyanates
- C08G18/8061—Masked polyisocyanates masked with compounds having only one group containing active hydrogen
- C08G18/8064—Masked polyisocyanates masked with compounds having only one group containing active hydrogen with monohydroxy compounds
- C08G18/8067—Masked polyisocyanates masked with compounds having only one group containing active hydrogen with monohydroxy compounds phenolic compounds
- C—CHEMISTRY; METALLURGY
- C06—EXPLOSIVES; MATCHES
- C06D—MEANS FOR GENERATING SMOKE OR MIST; GAS-ATTACK COMPOSITIONS; GENERATION OF GAS FOR BLASTING OR PROPULSION (CHEMICAL PART)
- C06D5/00—Generation of pressure gas, e.g. for blasting cartridges, starting cartridges, rockets
- C06D5/06—Generation of pressure gas, e.g. for blasting cartridges, starting cartridges, rockets by reaction of two or more solids
- 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
- C08L75/00—Compositions of polyureas or polyurethanes; Compositions of derivatives of such polymers
- C08L75/04—Polyurethanes

Landscapes

Chemical & Material Sciences (AREA)
Chemical Kinetics & Catalysis (AREA)
Organic Chemistry (AREA)
Health & Medical Sciences (AREA)
Medicinal Chemistry (AREA)
Polymers & Plastics (AREA)
Engineering & Computer Science (AREA)
Combustion & Propulsion (AREA)
Polyurethanes Or Polyureas (AREA)
Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Compositions Of Macromolecular Compounds (AREA)

SE7712842A 1976-11-15 1977-11-14 Herdbar komposition for anvendning vid framstellning av bundna polyuretandrivbrenslekorn SE434752B (sv)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
US05/741,591 US4098626A (en)	1976-11-15	1976-11-15	Hydroxy terminated polybutadiene based polyurethane bound propellant grains

Publications (2)

Publication Number	Publication Date
SE7712842L SE7712842L (sv)	1978-05-16
SE434752B true SE434752B (sv)	1984-08-13

Family

ID=24981349

Family Applications (2)

Application Number	Title	Priority Date	Filing Date
SE7712842A SE434752B (sv)	1976-11-15	1977-11-14	Herdbar komposition for anvendning vid framstellning av bundna polyuretandrivbrenslekorn
SE8201905A SE457079B (sv)	1976-11-15	1982-03-25	Drivbraenslekorn bundna med polyuretaner baserade paa polybutadiener med hydroxylaendgrupper och ett foerfarande foer dess framstaellning

Family Applications After (1)

Application Number	Title	Priority Date	Filing Date
SE8201905A SE457079B (sv)	1976-11-15	1982-03-25	Drivbraenslekorn bundna med polyuretaner baserade paa polybutadiener med hydroxylaendgrupper och ett foerfarande foer dess framstaellning

Country Status (8)

Country	Link
US (1)	US4098626A (cs)
JP (3)	JPS603330B2 (cs)
CA (1)	CA1111437A (cs)
DE (1)	DE2750701A1 (cs)
FR (1)	FR2370764A1 (cs)
GB (1)	GB1560981A (cs)
IL (1)	IL53186A (cs)
SE (2)	SE434752B (cs)

Families Citing this family (59)

* Cited by examiner, † Cited by third party
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US4165421A (en) *	1976-11-15	1979-08-21	Thiokol Corporation	Hydroxy terminated polybutadiene based polyurethane bound propellant grains
US4263444A (en) *	1977-09-26	1981-04-21	Thiokol Corporation	Hydroxy terminated polybutadiene based polyurethane bound propellant grains
US4391660A (en) *	1981-09-10	1983-07-05	The United States Of America As Represented By The Secretary Of The Air Force	Copper containing ballistic additives
US4482408A (en) *	1983-05-23	1984-11-13	The United States Of Amercia As Represented By The Secretary Of The Air Force	Plasticizer system for propellant compositions
US4482407A (en) *	1983-05-23	1984-11-13	The United States Of America As Represented By The Secretary Of The Air Force	Plasticizer system for propellant compositions
US4803019A (en) *	1984-02-10	1989-02-07	Morton Thiokol, Inc.	Process for forming a liner and cast propellant charge in a rocket motor casing
GB2159811A (en) *	1984-06-06	1985-12-11	Alan Richard Howard Bullock	Composite propellant
US5747603A (en) *	1987-05-19	1998-05-05	Thiokol Corporation	Polymers used in elastomeric binders for high-energy compositions
US5334270A (en) *	1992-01-29	1994-08-02	Thiokol Corporation	Controlled burn rate, reduced smoke, solid propellant formulations
US5771679A (en) *	1992-01-29	1998-06-30	Thiokol Corporation	Aluminized plateau-burning solid propellant formulations and methods for their use
JPH05263323A (ja) *	1992-12-02	1993-10-12	Howa Mach Ltd	カードのシリンダ制動装置
FR2719594A1 (fr) *	1994-05-04	1995-11-10	Rhone Poulenc Chimie	Isocyanates masqués au moyen de composés hydroxyaromatiques.
US6140452A (en) *	1994-05-06	2000-10-31	Advanced Bio Surfaces, Inc.	Biomaterial for in situ tissue repair
JP2002505592A (ja)	1996-11-15	2002-02-19	アドバンストバイオサーフェイシズ，インコーポレイティド	生体内原位置で組織を修復するのに用いる生体用材料システム
US8083745B2 (en)	2001-05-25	2011-12-27	Conformis, Inc.	Surgical tools for arthroplasty
US7468075B2 (en)	2001-05-25	2008-12-23	Conformis, Inc.	Methods and compositions for articular repair
US8545569B2 (en)	2001-05-25	2013-10-01	Conformis, Inc.	Patient selectable knee arthroplasty devices
US9603711B2 (en)	2001-05-25	2017-03-28	Conformis, Inc.	Patient-adapted and improved articular implants, designs and related guide tools
US8771365B2 (en)	2009-02-25	2014-07-08	Conformis, Inc.	Patient-adapted and improved orthopedic implants, designs, and related tools
US8556983B2 (en)	2001-05-25	2013-10-15	Conformis, Inc.	Patient-adapted and improved orthopedic implants, designs and related tools
US8735773B2 (en)	2007-02-14	2014-05-27	Conformis, Inc.	Implant device and method for manufacture
US8882847B2 (en)	2001-05-25	2014-11-11	Conformis, Inc.	Patient selectable knee joint arthroplasty devices
US7534263B2 (en)	2001-05-25	2009-05-19	Conformis, Inc.	Surgical tools facilitating increased accuracy, speed and simplicity in performing joint arthroplasty
US8480754B2 (en)	2001-05-25	2013-07-09	Conformis, Inc.	Patient-adapted and improved articular implants, designs and related guide tools
US20020035232A1 (en) *	1997-07-30	2002-03-21	Jean-Marie Bernard	Mixed masked isocyanate composition and its use in powdered paint
AU772012B2 (en)	1998-09-14	2004-04-08	Board Of Trustees Of The Leland Stanford Junior University	Assessing the condition of a joint and preventing damage
US7239908B1 (en)	1998-09-14	2007-07-03	The Board Of Trustees Of The Leland Stanford Junior University	Assessing the condition of a joint and devising treatment
AU2001290888B8 (en)	2000-09-14	2007-07-26	The Board Of Trustees Of The Leland Stanford Junior University	Assessing the condition of a joint and devising treatment
WO2002022013A1 (en)	2000-09-14	2002-03-21	The Board Of Trustees Of The Leland Stanford Junior University	Assessing condition of a joint and cartilage loss
US9308091B2 (en)	2001-05-25	2016-04-12	Conformis, Inc.	Devices and methods for treatment of facet and other joints
CN100502808C (zh)	2001-05-25	2009-06-24	肯弗默斯股份有限公司	用于关节表面再造的组合物
US8439926B2 (en)	2001-05-25	2013-05-14	Conformis, Inc.	Patient selectable joint arthroplasty devices and surgical tools
US6666934B2 (en)	2001-06-20	2003-12-23	Trw Inc.	Extruded hydroxy terminated polybutadiene gas generating material
WO2004032806A1 (en) *	2002-10-07	2004-04-22	Conformis, Inc.	Minimally invasive joint implant with 3-dimensional geometry matching the articular surfaces
CN1780594A (zh)	2002-11-07	2006-05-31	康复米斯公司	用于确定半月板的大小和形状以及设计治疗的方法
EP2671521A3 (en)	2006-02-06	2013-12-25	ConforMIS, Inc.	Patient selectable joint arthroplasty devices and surgical tools
US8623026B2 (en)	2006-02-06	2014-01-07	Conformis, Inc.	Patient selectable joint arthroplasty devices and surgical tools incorporating anatomical relief
EP2591756A1 (en)	2007-02-14	2013-05-15	Conformis, Inc.	Implant device and method for manufacture
WO2008157412A2 (en)	2007-06-13	2008-12-24	Conformis, Inc.	Surgical cutting guide
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1976
- 1976-11-15 US US05/741,591 patent/US4098626A/en not_active Expired - Lifetime
1977
- 1977-10-21 IL IL53186A patent/IL53186A/xx unknown
- 1977-11-08 CA CA290,446A patent/CA1111437A/en not_active Expired
- 1977-11-09 GB GB46726/77A patent/GB1560981A/en not_active Expired
- 1977-11-12 DE DE19772750701 patent/DE2750701A1/de active Pending
- 1977-11-14 FR FR7734148A patent/FR2370764A1/fr not_active Withdrawn
- 1977-11-14 SE SE7712842A patent/SE434752B/sv unknown
- 1977-11-15 JP JP52137194A patent/JPS603330B2/ja not_active Expired
1982
- 1982-03-25 SE SE8201905A patent/SE457079B/sv not_active IP Right Cessation
1983
- 1983-10-28 JP JP58202469A patent/JPS59193861A/ja active Granted
1984
- 1984-06-21 JP JP59128389A patent/JPS6042290A/ja active Granted

Also Published As

Publication number	Publication date
JPS6251947B2 (cs)	1987-11-02
JPS59193861A (ja)	1984-11-02
JPS5363349A (en)	1978-06-06
CA1111437A (en)	1981-10-27
JPS603330B2 (ja)	1985-01-28
SE8201905L (sv)	1982-03-25
JPS623116B2 (cs)	1987-01-23
US4098626A (en)	1978-07-04
DE2750701A1 (de)	1978-05-18
SE7712842L (sv)	1978-05-16
IL53186A (en)	1982-08-31
JPS6042290A (ja)	1985-03-06
FR2370764A1 (fr)	1978-06-09
SE457079B (sv)	1988-11-28
GB1560981A (en)	1980-02-13

Publication	Publication Date	Title
SE457079B (sv)	1988-11-28	Drivbraenslekorn bundna med polyuretaner baserade paa polybutadiener med hydroxylaendgrupper och ett foerfarande foer dess framstaellning
Bhowmik et al.	2015	An energetic binder for the formulation of advanced solid rocket propellants
US4263444A (en)	1981-04-21	Hydroxy terminated polybutadiene based polyurethane bound propellant grains
AU2003200305B2 (en)	2008-04-03	Semi-continuous two-component process for producing a composite explosive charge comprising a polyurethane matrix
US4775432A (en)	1988-10-04	High molecular weight polycaprolactone prepolymers used in high-energy formulations
SE437523B (sv)	1985-03-04	Forfarande och medel for reglering av brukstid och herdningshastighet av ett drivmedelskorn baserat pa polyuretanbindemedel
US5872328A (en)	1999-02-16	Ferrocene derivatives
US20180290945A1 (en)	2018-10-11	HIGH PERFORMANCE COMPOSITE PYROTECHNIC PRODUCT WITHOUT Pb IN ITS COMPOSITION, AND PREPARATION THEREOF
SU862833A3 (ru)	1981-09-07	Состав дл покрытий
US4165421A (en)	1979-08-21	Hydroxy terminated polybutadiene based polyurethane bound propellant grains
US4234738A (en)	1980-11-18	Hydroxy terminated polybutadiene based polyurethane bound propellant grains
JPS5848882B2 (ja)	1983-10-31	ネツコウカセイポリウレタンセイメガネフレ−ム
IE41439B1 (en)	1980-01-02	A biuret polyisocyanate mixture stabilised against monomer reversion
US6042663A (en)	2000-03-28	Propellant compositions with nitrocellulose and a polymer
AU605314B2 (en)	1991-01-10	Energetic azido curing agents
US3242139A (en)	1966-03-22	Polyurethane compositions based on 3, 11-dioxa-5, 7, 9-trinitraza-1, 13-tridecanediol
US4050969A (en)	1977-09-27	Catalytic system and polyurethane propellants
US4038113A (en)	1977-07-26	Catalyst system for polyurethane propellants
US4482407A (en)	1984-11-13	Plasticizer system for propellant compositions
Gupta et al.	1997	HTPB‐based polyurethanes for inhibition of composite‐modified double‐base (CMDB) propellants
JP3132524B2 (ja)	2001-02-05	コンポジット推進薬
JP2799740B2 (ja)	1998-09-21	ダブルベース系推進薬組成物及び該組成物の製造方法
JPS6071625A (ja)	1985-04-23	無機物充填ポリウレタン系樹脂の製造方法
JPS59128291A (ja)	1984-07-24	ポリジエン系コンポジツト推進薬の粘結剤
GB2257968A (en)	1993-01-27	Preparation of composite double base propellants