Aeronautics and astronautics – Aircraft structure – Fuel supply
Reexamination Certificate
1999-05-11
2002-01-01
Barefoot, Galen L. (Department: 3644)
Aeronautics and astronautics
Aircraft structure
Fuel supply
C244S158700, C220S495040, C220S003940
Reexamination Certificate
active
06334589
ABSTRACT:
REFERENCE TO A “MICROFICHE APPENDIX”
Not applicable
BACKGROUND OF THE INVENTION
1. Field of the Invention:
This invention relates in general to oxygen containment tanks and feedline systems for use with a launch vehicle herein the tanks is of composite material construction and more specifically to resins whose chemical structure contains cyanate linkages.
2. General Background:
The development of polymer composite liquid oxygen tanks is a critical step in creating the next generation of launch vehicles. Future reusable launch vehicles need to minimize the gross liftoff weight (GLOW) by reducing the dry mass fraction. The (dry) mass fraction is the weight of the launch vehicle without fuel divided by the weight of the vehicle with fuel.
FIG. 1
is graph showing the effect of mass fraction on GLOW. Indicated on the graph are the RLV mass fraction target region as well as the mass fraction of the RLV without the weight reduction that composites could provide. It is clear that composite tanks are critical to enable future launch vehicles to meet required mass fractions.
The required mass fraction is possible due to the reduction of weight that composite materials can provide. Traditional oxygen tanks are usually made from metals. The space shuttle external tank (ET) has historically been made from 2219 aluminum and more recently 2195 aluminum/lithium alloy.
FIG. 2
shows a comparison between these two aluminum alloys and a typical composite material for a liquid oxygen tank for a launch vehicle. The chart shows that a composite tank provides up to 41% and 28% weight savings when compared to 2219 and 2195 aluminum tanks, respectively.
Although a composite lox tank makes RLV mass fractions feasible, a liquid oxygen tank must be compatible with oxygen. The ASTM definition for oxygen compatibility is the “ability of a substance to coexist with both oxygen and a potential source(s) of ignition within the acceptable risk parameter of the user.” It is imperative that materials are selected that will resist any type of detrimental, combustible reaction when exposed to usage environments. Typically, non-metallic materials are not used in these applications because most are easily ignited in the presence of oxygen. However, there are some polymeric materials with inert chemistries that may be used for this application and resist ignition. These chemistries were evaluated by fabricating coupons and testing them with various ignition mechanisms in the presence of liquid and gaseous oxygen. The testing performed reflected situations in launch vehicles that could be potential sources of ignition in composite. These tests included pressurized mechanical impact, particle impact, puncture, puncture of damaged, oxygen-soaked samples, electrostatic discharge, friction, and pyrotechnic shock. An example of a polymeric material system that resisted reaction to these mechanisms were cyanate ester composites.
Applications include liquid oxygen for future launch vehicles, such as the Lockheed Martin Reusable Launch Vehicle (RLV). They could also potentially be used in other aerospace applications, including but not limited to, RFP (rocket fuel propellant) tanks and crew vehicle cabins. Other industries that may be interested in composite oxygen tanks include the air handling and medical industries. The ability to resist ignition may also useful in chemical storage tanks and NGV (natural gas vehicle) tanks.
The following U.S. Patents are incorporated herein by reference: 5,056,367; 5,251,487; 5,380,768; 5,403,537; 5,419,139; and all references cited in those patents.
The following international applications published under the PCT are incorporated herein by reference: International Publication Nos. WO 97/18081 and WO 97/28401 and all references cited in those publications.
SUMMARY OF INVENTION
Inifo on Resins and Fibers
A fiber-reinforced composite is defined as a material consisting of fibers of high strength and modulus embedded in or bonded to a matrix with distinct interfaces or boundaries between them. In this form, both fibers and matrix retain their physical and chemical identities, yet they produce a combination of properties that cannot be produced by either constituent alone. In general, fibers are the principal load carrying members, while the surrounding matrix keeps them in desired location and orientation, transfers loads between fibers, and protects the fibers. The matrix material may be a polymer, a metal, or a ceramic. This patent focuses on polymer matrix composites.
The fibers can be made from a variety of materials. These materials include glass, graphite or carbon, polymers, boron, ceramics, or metals. Glass fibers include E-glass (electrical) and S-glass (structural) types. Carbon fibers include those made from different precursors, such as polyacrylonitrile (PAN) or pitch. Polymer fibers include, but are not limited to, aramid (Kevlar®), polyethylene (Spectra(®), or PBO (Zylon(®). Ceramic fibers may include silicon carbide (SiC) or aluminum oxide (Al203).
For cryogenic tanks, the preferred matrix material is a polymer. The preferred fiber is carbon fiber, more preferably PAN-based fibers, more preferably high strength (over 500 ksi) and high modulus (over 30 Msi) fibers. The most preferred fibers are ultra high modulus fibers (over 60 Msi), specifically M55J fiber by Toray.
Info on Toughness/Microcracking
Another critical parameter for a composite tank is the ability to withstand repeated temperature changes (thermal cycles) without microcracking. One factor that contributes to microcrack resistance is toughness.
The present invention provides a liquid oxygen tank of composite material, a fiber-reinforced cyanate ester composite. A cyanate ester material is one that is made from cyanate monomers or oligomers. A cyanate monomer or oligimer is characterized by a reactive cyanate end group, which is an OCN on an aromatic ring. See
FIG. 3
for a characteristic cyanate monomer.
Cyanate polymer networks are formed by applying energy, usually heat, to the monomers. The polymer structure consists of oxygen-linked triazine rings (cyanurates) and ester groups. This unique structure results from the cyclotrimerization (ring made of three monomers) of the R-OCN group of atoms. See
FIG. 4
for a diagram of this process.
Cyanate ester resins may also contain bonds with halogens, such as bromine, to further enhance their O2 compatibility performance.
Several cyanate resins and composites have been subjected to an extensive battery of tests for their sensitivity to reaction in the presence of oxygen. Historically, the approach was to test the material in the standard mechanical impact test in liquid oxygen (LOX). The mechanical impact threshold is preferably between 10 and 72 foot pounds. Ideally, if the material had an impact threshold of 72 foot-pounds, it was acceptable for use in oxygen environments, such as launch vehicle LOX tanks. If the material's threshold was less than 72 foot-pounds, it typically was not used. Due to limitations in the testing as well as differences in the material structures between metals and composites, standard high-strength composite materials typically have not been able to pass at this level at RLV tank wall thicknesses. The approach taken here, which was developed in conjunction with NASA, was to use the standard mechanical impact test to rank composites with respect to each other. Furthermore, an evaluation of the compatibility of composites in oxygen environments would only be determined after testing composite materials with respect to specific ignition mechanisms while in the presence of oxygen. The ignition mechanisms tested included pressurized mechanical impact, particle impact, puncture, puncture of damaged, oxygen-soaked samples, electrostatic discharge, friction, and pyrotechnic shock. If the material could withstand ignition in these environments, it could possibly be considered oxygen compatible.
Several cyanate ester materials have been evaluated in the standard mechanical impact test. Many of these cyanate ester materials were tested in b
Ely Kevin Wilbur
Graf Neil Anthony
Kirn Elizabeth P.
Barefoot Galen L.
Garvey, Smith, Nehrbass & Doody, L.L.C.
Lockheed Martin Corporation
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