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US4806613A
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Method of producing thermoplastic elastomers having alternate crystalline structure for use as binders in high-energy compositions
Assignee: Northrop Grumman Innovation Systems LLC
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Filing: 1988-03-29
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Granted: 1989-02-21
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Expires: 2008-03-29
Abstract
Abstract A method of preparing a thermoplastic elastomer having A blocks and at least one B block, wherein said A blocks are crystalline at temperatures below about 60° C. and said B block(s) is amorphous at temperatures above about -20° C., said A blocks each being polyethers derived from monomers of oxetane and its derivatives and/or tetrahydrofuran and its derivatives, the method comprising providing hydroxyl terminated A blocks which are crystalline at temperatures below about 60° C. and separately providing hydroxyl terminated B blocks which are amorphous at temperatures above about -20° C., end-capping said A blocks and said B blocks by separately reacting each of said A blocks and B blocks with a diisocyanate in which one isocyanate moiety is at least about five times as reactive with the terminal hydroxyl groups of each of the blocks as the other isocyanate moiety, whereby the more reactive isocyanate moiety tends to react with terminal hydroxyl groups of the blocks, leaving the less reactive isocyanate moiety free and unreacted, mixing said end-capped A blocks and said end-capped B blocks together at approximately the stoichiometric ratios that they are intended to be present in the thermoplastic elastomer, and reacting said mixture with a linking compound having two isocyanate-reactive groups which are sufficiently unhindered to react with the free isocyanate groups of said end-capped polymer.
Inventors
- 👤 Robert B. Wardle
Bibliographic Details
Application Number
—
Jurisdiction
US
Data Source
google_patents
Last Synchronized
2026-10-23 20:18
CPC Classifications
C; C08; C08G; C08G18/00; C08G18/06; C08G18/70; C08G18/72; C08G18/74; C08G18/76; C08G18/7614; C08G18/7621; C08G18/08; C08G18/10; C08G18/12; C08G18/28; C08G18/40; C08G18/48; C08G18/4854; C08G18/4858; C08G18/50; C08G18/5003; C08G18/5021; C08G18/67; C08G18/6795; C08G18/75; C08G18/751; C08G18/752; C08G18/753; C08G18/755; C08G2250/00
Claims Analysis
Total Claims: 17
Claim 1
Independent Claim
221 words
A method of preparing a thermoplastic elastomer having A blocks and at least one B block, wherein said A blocks are crystalline at temperatures below about 60° C. and said B block(s) is amorphous at temperatures above about -20° C., said A blocks each being polyethers derived from monomers of oxetane and its derivatives and/or tetrahydrofuran and its derivatives, the method comprising providing hydroxyl terminated A blocks which are crystalline at temperatures below about 60° C. and separately providing hydroxyl terminated B blocks which are amorphous at temperatures above about -20° C., end-capping said A blocks and said B blocks by separately reacting each of said A blocks and B blocks with a diisocyanate in which one isocyanate moiety is at least about five times as reactive with the terminal hydroxyl groups of each of the blocks as the other isocyanate moiety, whereby the more reactive isocyanate moiety tends to react with terminal hydroxyl groups of the blocks, leaving the less reactive isocyanate moiety free and unreacted, mixing said end-capped A blocks and said end-capped B blocks together at approximately the stoichiometric ratios that they are intended to be present in the thermoplastic elastomer, and reacting said mixture with a linking compound having two isocyanate-reactive groups which are sufficiently unhindered to react with the free isocyanate groups of said end-capped polymer.
Claim 2
Independent Claim
221 words
A method of preparing a thermoplastic elastomer having A blocks and at least one B block, wherein said A blocks are crystalline at temperatures below about 60° C. and said B block(s) is amorphous at temperatures above about -20° C., said A blocks each being polyethers derived from monomers of oxetane and its derivatives and/or tetrahydrofuran and its derivatives, the method comprising providing hydroxyl terminated A blocks which are crystalline at temperatures below about 60° C. and separately providing hydroxyl terminated B blocks which are amorphous at temperatures above about -20° C., end-capping said A blocks and said B blocks by separately reacting each of said A blocks and B blocks with a diisocyanate in which one isocyanate moiety is at least about five times as reactive with the terminal hydroxyl groups of each of the blocks as the other isocyanate moiety, whereby the more reactive isocyanate moiety tends to react with terminal hydroxyl groups of the blocks, leaving the less reactive isocyanate moiety free and unreacted, mixing said end-capped A blocks and said end-capped B blocks together at approximately the stoichiometric ratios that they are intended to be present in the thermoplastic elastomer, and reacting said mixture with a linking compound having two isocyanate-reactive groups which are sufficiently unhindered to react with the free isocyanate groups of said end-capped polymer.
Claim 3
Dependent Claim
100 words
The method according to claim 1 wherein said oxetane momomers have the general formula: ##STR5## wherein the R groups are the same or different and are selected from moieties having the general formulae: --(CH 2 ) n X, where n is 0-10 and X is selected from the group consisting of --H, --NO 2 , --CN, --Cl, F, --O-alkyl, --OH, --I, --ONO 2 , --N(NO 2 )-alkyl, --C.tbd.CH, --Br, --CH═CH(H or alkyl), --O--CO--(H or alkyl), --CO 2 --(H or alkyl), --N(H or alkyl) 2 , --O--(CH 2 ) 1-5 --O--(CH 2 ) 0-8 --CH 3 , and --N 3 .
Claim 4
Dependent Claim
100 words
A method according to claim 1 wherein said THF monomers have the general formula: ##STR6## wherein the R groups are the same or different and are selected from moieties having the general formulae: --(CH 2 ) n X, where n is 0-10 and X is selected from the group consisting of --H, --NO 2 , --CN, --Cl, F, --O--alkyl, --OH, --I, --ONO 2 , --N(NO 2 )-alkyl, --C.tbd.CH, --Br, --CH═CH(H or alkyl), --O--CO--(H or alkyl), --CO 2 --(H or alkyl), --N(H or alkyl) 2 , --O--(CH 2 ) 1-5 --O--(CH 2 ) 0-8 --CH 3 , and --N 3 .
Claim 5
Dependent Claim
38 words
A method according to claim 1 wherein said B block(s) has a molecular weight of between about 5000 and about 50,000 and each of said A blocks has a molecular weight of between about 3000 and about 12,500.
Claim 6
Dependent Claim
36 words
A method according to claim 1 wherein said A blocks together have a molecular weight between about 1/3 and about 1 times the molecular weight of said B block or total weight of said B blocks.
Claim 7
Dependent Claim
22 words
A method according to claim 1 wherein said A block is selected from the group consisting of poly(3,3-bis(ethoxymethyl)oxetane), poly(3,3-bis(methoxymethyl)oxetane), poly(3,3-bis(fluromethyl)oxetane), and poly(3,3-bis(azidomethyl)oxetane).
Claim 8
Dependent Claim
33 words
A method according to claim 1 wherein said B block is selected from poly(3-azidomethyl-3-methyloxetane, (3-azidomethyl-3-methyloxetane)/3,3-bis(azidomethyl)oxetane copolymer, tetrahydrofuran/3,3-bis(azidomethyl)oxetane copolymer, tetrahydrofuran/3-azidomethyl-3-methyloxetane copolymer, tetrahydrofuran/3-octoxymethyl-3-methyloxetane copolymer, tetrahydrofuran/3,3-bis(methyoxyethoxymethyl)oxetane copolymer, tetrahydrofuran/3,3-bis(ethoxymethyl)oxetane copolymer, tetrahydrofuran/3,3-bis(methoxymethyl)oxetane copolymer, tetrahydrofuran/3,3-bis(fluromethyl)oxetane copolymer, poly(3-nitratomethyl-3-methyloxetane), and 3,3-bis(azidomethyl)oxetane/3-nitratomethyl-3-methyloxetane)coploymer.
Claim 9
Dependent Claim
37 words
A method according to claim 1 wherein said oxetane monomers are selected from the group consisting of: 3,3-bis(ethoxymethyl)oxetane, 3,3-bis(chloromethyl)oxetane, 3,3-bis(methoxymethyl)oxetane, 3,3-bis(fluromethyl)oxetane, 3-hydroxymethyl-3-methyloxetane, 3,3-bis(acetoxymethyl)oxetane, 3,3-bis(hydroxymethyl)oxetane, 3-octoxymethyl-3-methyloxetane, 3,3-bis(methoxyethoxymethyl)oxetane, 3-chloromethyl-3-methyloxetane, 3-azidomethyl-3-methyloxetane, 3-3-bis(iodomethyl)oxetane, 3-iodomethyl-3-methyloxetane, 3-propynomethylmethyloxetane, 3,3-bis(nitratomethyl)oxetane, 3-nitratomethyl-3-methyloxetane, 3,3-bis(methylnitraminomethyl)oxetane, 3-methylnitraminomethyl-3-methyloxetane, and 3,3-bis(azidomethyl)oxetane.
Claim 10
Dependent Claim
8 words
The product of the process of claim 1.
Claim 11
Dependent Claim
10 words
(3,3-bis(ethoxymethyl)oxetanetetrahydrofuran/3,3-bis(methoxymethyl)oxetane) n produced according to the method of claim 1.
Claim 12
Dependent Claim
9 words
(3,3-bis(ethoxymethyl)oxetane-3,3-bis(azidomethyl)oxetane/3-azidomethyl-3-methyloxetane).sub.n prepared according to the method of claim 1.
Claim 13
Dependent Claim
12 words
A method according to claim 1 wherein said diisocyanate is toluene diisocyanate.
Claim 14
Dependent Claim
12 words
A method according to claim 1 wherein said diisocyanate is isophorone diisocyanate.
Claim 15
Dependent Claim
27 words
A method according to claim 1 wherein said end-capping reaction and said reaction with said linking compound are each conducted in the presence of a urethane catalyst.
Claim 16
Dependent Claim
46 words
A method according to claim 1 wherein each of said A blocks and said B blocks are difunctional and said linking compound is provided at about a 0.4 to 0.6 molar ratio relative to total A and B blocks, whereby an (AB) n polymer is produced.
Claim 17
Dependent Claim
38 words
A method according to claim 1 wherein in said end-capping reaction, when either of said blocks has a pair of terminal hydroxyl groups, said diisocyanate is provided at between about a 1.75 and about a 2.2 molar ratio.
References Cited (Backward Citations)
USPTO Annuity & Maintenance Windows
| Annuity Stage | Window Opens | Payment Deadline | Surcharge Period Until | Estimated Fee | Status |
|---|---|---|---|---|---|
| 3.5 Years (Year 4) | 1992-02-21 | 1992-08-22 | 1993-02-21 | $2000.00 | Window Closed / Lapsed |
| 7.5 Years (Year 8) | 1996-02-21 | 1996-08-22 | 1997-02-21 | $3760.00 | Window Closed / Lapsed |
| 11.5 Years (Year 12) | 2000-02-21 | 2000-08-22 | 2001-02-21 | $7700.00 | Window Closed / Lapsed |