IP Library Granted Patent US 12,560,135
Granted Patent B2
US 12,560,135 · App. 18/064,703 · Granted Feb 24, 2026

Precursor compositions for an insulation and related methods

Inventors: Himansu M. Gajiwala (Layton, UT); Steven B. Hall (Perry, UT)
Assignee: Northrop Grumman Systems Corporation
F02K9/346C08K3/04C08L9/00C08L23/083C08L23/145C08L23/16C08L77/10F02K9/34
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Quick Facts
Patent No.
US 12,560,135
App. No.
18/064,703
Granted
Feb 24, 2026
Kind
B2
Abstract

A precursor composition comprising, before curing, ethylene propylene diene monomer (EPDM), an aramid, and a carbon material comprising carbon nanotubes, graphite, or a combination thereof. A rocket motor including a reaction product of the precursor composition and a method of insulating a rocket motor are also disclosed.

Claims (62)

1. A precursor composition, consisting of, before curing:

ethylene propylene diene monomer (EPDM);

an aramid;

multi-walled carbon nanotubes in an amount of from about 15.0 parts by weight to about 30.0 parts by weight of the precursor composition;

expandable graphite in an amount of from about 1.0 parts by weight to about 10.0 parts by weight of the precursor composition;

a plasticizer;

one or more of zinc oxide, silica, or magnesium hydroxide;

a chlorinated organic compound;

trimethylolpropane trimethacrylate or a poly(butadiene) resin;

an antioxidant;

a fatty acid; and

a peroxide,

wherein after curing, the precursor composition provides an insulation material exhibiting an ablative performance suitable for use in various regions of a rocket motor.

2. The precursor composition of claim 1 , wherein the plasticizer is an aliphatic resin.

3. The precursor composition of claim 1 , wherein the plasticizer is a five carbon petroleum hydrocarbon.

4. The precursor composition of claim 1 , wherein the chlorinated organic compound is a solid chlorinated paraffin.

5. The precursor composition of claim 1 , wherein the antioxidant is a hydroquinoline compound, an amine compound, a phenol compound, or a combination thereof.

6. The precursor composition of claim 1 , wherein the antioxidant is a polymerized 1,2 dihydro-2,2,4-trimethylquinoline.

7. The precursor composition of claim 1 , wherein the fatty acid is stearic acid.

8. The precursor composition of claim 1 , wherein the peroxide is 1,1-di-(t-butylperoxy)-3,3,5-trimethylcyclohexane or dicumyl peroxide.

9. A precursor composition, comprising, before curing:

ethylene propylene diene monomer (EPDM);

poly-p-phenylene terephthalamide;

multi-walled carbon nanotubes in an amount of from about 15.0 parts by weight to about 30.0 parts by weight of the precursor composition;

expandable graphite in an amount of from about 1.0 parts by weight to about 10.0 parts by weight of the precursor composition;

a five carbon petroleum hydrocarbon;

magnesium hydroxide;

a solid chlorinated paraffin;

a poly(butadiene) resin;

a hydroquinoline compound;

a fatty acid; and

1,1-di-(t-butylperoxy)-3,3,5-trimethylcyclohexane or dicumyl peroxide,

wherein after curing, the precursor composition provides an insulation material exhibiting an ablative performance suitable for use in various regions of a rocket motor.

10. The precursor composition of claim 9 , wherein the hydroquinoline compound is a polymerized 1,2 dihydro-2,2,4-trimethylquinoline.

11. The precursor composition of claim 9 , wherein the poly-p-phenylene terephthalamide is poly-p-phenylene terephthalamide fibers or poly-p-phenylene terephthalamide pulp.

12. A precursor composition, consisting of, before curing:

ethylene propylene diene monomer (EPDM);

poly-p-phenylene terephthalamide;

multi-walled carbon nanotubes in an amount of from about 15.0 parts by weight to about 30.0 parts by weight of the precursor composition;

expandable graphite in an amount of from about 1.0 parts by weight to about 10.0 parts by weight of the precursor composition;

a five carbon petroleum hydrocarbon;

magnesium hydroxide;

a solid chlorinated paraffin;

a poly(butadiene) resin;

a polymerized 1,2 dihydro-2,2,4-trimethylquinoline;

stearic acid; and

dicumyl peroxide,

wherein after curing, the precursor composition provides an insulation material exhibiting an ablative performance suitable for use in various regions of a rocket motor.

13. The precursor composition of claim 12 , wherein the poly(butadiene) resin is a high vinyl poly(butadiene).

14. A precursor composition, consisting of, before curing:

ethylene propylene diene monomer (EPDM);

an aramid;

multi-walled carbon nanotubes in an amount of from about 15.0 parts by weight to about 30.0 by weight of the precursor composition;

expandable graphite in an amount of from about 1.0 parts by weight to about 10.0 parts by weight of the precursor composition;

a plasticizer;

one or more of zinc oxide, silica, or magnesium hydroxide;

a chlorinated organic compound;

a co-agent;

an antioxidant;

a fatty acid; and

a peroxide,

wherein after curing, the precursor composition provides an insulation material exhibiting an ablative performance suitable for use in various regions of a rocket motor.

Continuity (2)
Continuation 15793862 · Oct 25, 2017
Related Publication 20230287848A1 · Sep 14, 2023
References Cited (67)
US 2303329A · Cyr · 1942 [cited by applicant]
US 4878431A · Herring · 1989 [cited by applicant]
US 5352312A · Guillot · 1994 [cited by applicant]
US 5821284A · Graham et al. · 1998 [cited by applicant]
US 6566420B1 · Guillot et al. · 2003 [cited by applicant]
US 6606852B1 · Harvey et al. · 2003 [cited by applicant]
US 6691505B2 · Harvey et al. · 2004 [cited by applicant]
US 6953823B2 · Fan · 2005 [cited by applicant]
US 7012107B2 · Harvey et al. · 2006 [cited by applicant]
US 7070705B2 · Harvey et al. · 2006 [cited by applicant]
US 7410607B2 · Guillot · 2008 [cited by applicant]
US 7461503B2 · Gajiwala · 2008 [cited by applicant]
US 7485060B2 · Hineno et al. · 2009 [cited by applicant]
US 7767746B2 · Gajiwala · 2010 [cited by applicant]
US 10612492B2 · Gajiwala et al. · 2020 [cited by applicant]
US 20020018847A1 · Guillot · 2002 [cited by applicant]
US 20020189233A1 · Harvey et al. · 2002 [cited by applicant]
US 20030181545A1 · Barboric et al. · 2003 [cited by applicant]
US 20040106732A1 · Tsuji et al. · 2004 [cited by applicant]
US 20070112091A1 · Fan et al. · 2007 [cited by applicant]
US 20070112136A1 · Nakano et al. · 2007 [cited by applicant]
US 20070270540A1 · Kanae et al. · 2007 [cited by applicant]
US 20090137700A1 · Gajiwala · 2009 [cited by applicant]
US 20100210770A1 · Nadeau et al. · 2010 [cited by applicant]
US 20110086735A1 · Takahashi et al. · 2011 [cited by applicant]
US 20110186775A1 · Shah et al. · 2011 [cited by applicant]
US 20120021860A1 · Matsuda · 2012 [cited by applicant]
US 20120153242A1 · Le Bonte et al. · 2012 [cited by applicant]
US 20140011963A1 · Mccauley et al. · 2014 [cited by applicant]
US 20140255635A1 · Morgan et al. · 2014 [cited by applicant]
US 20150203668A1 · Bedard et al. · 2015 [cited by applicant]
US 20180265686A1 · Gajiwala et al. · 2018 [cited by applicant]
US 20180265692A1 · Gajiwala et al. · 2018 [cited by applicant]
US 20190120174A1 · Gajiwala et al. · 2019 [cited by applicant]
CN 105754273A · 2016 [cited by applicant]
CN 107057196A · 2017 [cited by applicant]
CN 104875467B · 2017 [cited by applicant]
EP 0116453A2 · 1984 [cited by applicant]
EP 0569995A1 · 1998 [cited by applicant]
EP 3045770A1 · 2016 [cited by applicant]
EP 3184585A1 · 2017 [cited by applicant]
JP 59174340A · 1984 [cited by applicant]
JP 2002535812A · 2002 [cited by applicant]
JP 2003504474A · 2003 [cited by applicant]
JP 2011174004A · 2011 [cited by applicant]
WO 0104198A1 · 2001 [cited by applicant]
WO 2014168979A1 · 2014 [cited by applicant]
Asbury Carbons “Expandable Graphite”; Accessed Oct. 17, 2017 at https://asbury.com/brochures-literature/brochures-2/; (2 pages); Asbury Carbon Anthracite Industries Division. [cited by applicant]
Corrosionpedia, “Hydrocarbon Solvent”, https://www.corrosionpedia.com/definition/2182/hydrocarbon-solvent#:˜:text=Corrosionpedia%20explains%20Hydrocarbon%20Solvent&text=Frequently%20used%20aliphatic%20hydrocarbon%20solv… [cited by applicant]
Cray Valley USA, LLC, “Use of Polybutadiene Coagents in Peroxide Cured Elastomers for Wire and Cable Compounds”, 01/10, 19 pages, Dec. 1, 1995. [cited by applicant]
DOW Technical Information, Nordel IP 4520 Hydrocarbon Rubber, 2 pages; Form No. 400-00084029en, Rev: Jan. 11, 2012. [cited by applicant]
Encyclopaedia Britannica “Paraffin hydrocarbon Chemical Compound” Article, 1 page; https://www.britannica.com/science/paraffin-hydrocarbon; accessed Nov. 14, 2019. [cited by applicant]
European Communication pursuant to Article 94(3) EPC for European Application No. 18200704.7, dated Jan. 12, 2022, 4 pages. [cited by applicant]
European Extended Search Report and Opinion for European Application No. 18200704.7, dated Mar. 19, 2019, 6 pages. [cited by applicant]
Graphistrength Advanced Materials, Graphistrength EPDM; CNT Masterbatch Technical Data Sheet (2 pages). [cited by applicant]
Lanxess Deutschland GmbH, “KELTAN 2650 Product Data Sheet” Issue No. LX10/Publication issued Sep. 24, 2013, 2 pages. [cited by applicant]
Lanxess Energizing Chemistry, Buna® EP, Ethylene Propylene Rubber, The Versatile Elastomer, Edition May 2007, Publication, May 2007, 24 pages. [cited by applicant]
Martin Marietta Magnesia Specialties, LLC “MagShield (Registered) S Standard Grade Magnesium Hydroxide for Flame Retardant Applications” Copyright (Copyright) 2015 by Martin Marietta Magnesia Specialties, LLC Version Ja… [cited by applicant]
Moore et al., “Reusable Solid Rocket Motor—Accomplishments, Lessons, and a Culture of Success” Article, NASA Marshall Space Flight Center; Huntsville, Alabama, (2011), 28 pages. [cited by applicant]
Nordel EPDM Product Selection Guide, Published Apr. 2014, (Copyright) 2014 The Dow Chemical Company, 8 pages. [cited by applicant]
OxyChem Dechlorane Plus Manual, CAS Registry No. 13560-89-9, 51 Pages; https://www.oxy.com/OurBusinesses/Chemicals/Products/Documents/dechloraneplus/dechlorane_plus.pdf; accessed Nov. 14, 2019. [cited by applicant]
Polymer Properties Database, Hydrocarbon Resins (C5 and C9 Resins), https://polymerdatabase.com/polymer%20classes/Hydrocarbon%20resins.html#:˜:text=These%20resins%20are%20available%20in,100%20to%20150%C2%BOC.&text=C9%20… [cited by applicant]
Prasher et al. “Turning Carbon Nanotubes from Exceptional Heat Conductors into Insulators” Physical Review Letters 102, 105901 (2009) 4 pages. [cited by applicant]
Puyang Ruicheng Checmical Co., Ltd, “Petroleum Resin”, http://pyrchg.com/petroleum-resin/, Last Accessed Jan. 20, 2021, 8 pages. [cited by applicant]
Search Report in European Application No. 18160620.3 dated May 25, 2018, 6 pages. [cited by applicant]
Shell Chemicals, “n-Pentane Data Sheet”, Nov. 21, 2007, https://www.shell.com/business-customers/chemicals/our-products/solvents-hydrocarbon/pentanes/n-pentane/_jcr_content/par/tabbedcontent/tab/textimage.stream/1519786… [cited by applicant]
Teijin “Twaron—a versatile high-performance fiber”, brochure (7 pages) accessed Oct. 17, 2017 at: http://www.teijinaramid.com/wp-content/uploads/2017/07/Twaron-product-brochure-English.pdf. [cited by applicant]