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Title: Flexible thermal control
composite
United States Patent: 7,067,580
Issued: June 27, 2006
Inventors: Hayes; Claude Q. C.
(San Diego, CA)
Appl. No.: 831948
Filed: April 26, 2004
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Woodbury College's
Master of Science in Law
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Abstract
A flexible thermal control composite
comprising a natural or synthetic polymer and an endotherm dispersed,
distributed and suspended within said natural or synthetic polymer i.e. "P"olymer
"C"ontaining an "E"ndothermic "A"gent (PCEA). The PCEA can be formed into
thin and thick films. It can be drawn, molded, extruded and spun into
fibers or all dimensions. It can be formed and chopped into PCEA mulch.
Irrespective its final form, the PCEA can be used in insulating,
thermoprotecting, heat absorbing applications on the one hand, and heat
maintenance applications of all types on the other.
SUMMARY OF THE
INVENTION
The inventive composition of matter is a
flexible thermal control composite. Said composite comprises a polymer and
an endothermic agent. The endothermic agent is dispersed, distributed, and
suspended in the polymer. Thereafter it is cured to form a "P"olymer "C"ontaining
an "E"ndothermic "A"gent (PCEA) composite. This composite now has thermal
control properties that make it suitable for a multitude of thermal
control applications.
Natural or synthetic polymer may be softened or liquified by being (1)
heated, (2) dissolved or (3) suspended in a plasticizer or solvent. When
the polymer treated in any of these manners has an endothermic agent added
to it, in very specific concentrations, distributed, dispersed, suspended
therein and cured, a thermal control composite i.e. a PCEA is formed. Such
PCEA is in essence capable of thermal control through its ability to
absorb and store heat or through its ability to first absorb heat and then
release it. It does so through the use of its endothermic compounds' own
inherent thermodynamic, physical and chemical properties, i.e. their
latent heats of fusion, hydration, formation, decomposition, vaporization,
sublimation, or its allotropic and phase change reactions; while
simultaneously completely eliminating any possibility of leakage of its
endothermic compounds into the environment, as said agents become an
integral part of the PCEA overall physical structure.
Thus, according to the present invention there is provided a PCEA thermal
control composite comprising a natural or synthetic polymer and an
endothermic agent. The PCEA thermal control composite can be thin, as for
example a thin or a thick film, or molded as a thick PCEA brick. When the
PCEA is a thin film, then the effective distribution of the endothermic
agents within said polymer is 0.0001 to 1.2 gram of endothermic or thermal
storage compound per square inch of PCEA, the PCEA having a thickness of
0.05 to 2.0 mil. On the other hand, where the PCEA is a thick film or
molded structure, then the effective concentration of endotherm will be
0.05% 60% by weight endotherm in PCEA.
DETAILED DESCRIPTION
OF THE PREFERRED EMBODIMENT
The inventive thermal control composite
i.e. the PCEA material 10 of FIG. 1, FIG. 2, FIG. 3, and FIG. 4 (see Original Patent)
shows the endothermic agent 11 dispersed, distributed and suspended within
a polymer or plastic 12.
(a) The Polymer or Plastic.
The plastic or polymer 12 of the PCEA material 10 may comprise any natural
or synthetic polymer or a mixture thereof. Such natural and synthetic
polymers comprise: all latexes including those used in paint;
fluoropolymers such as various TEFLON.RTM. species, specifically
polytetrafluoroethylene (PTFE), polyfluoroacetate (PFA) and
fluoroethylpropylene(FEP) and other fluorinated plastic films having
similar thermal stability, i.e. FEP: -200 DEGREES C. TO 200 DEGREES C. and
PFA: -200 DEGREES C. TO 250 DEGREES C., that are well known in the art;
expanded TEFLON.RTM.; high temperature fluoroelastomers such as VITON.RTM.
and other highly thermoresistant polymers and plastics well known in the
art; elastomers such as SILICONE.RTM. species specifically
polydimethylsiloxane and polymethylphenylsiloxane and other siloxanes well
known in the art; polyimides such as KAPTON.RTM.; POLYESTERS.RTM. such as
MYLAR.RTM.; high density polymers such as TIVAR.RTM. and SPECTRA.RTM.; and
other polyamides, polyarylates, polyetherimides, polyketones,
polyphenylene oxides or sulfides, polyphenylsulfones, polystilfones,
acetals, nylons, ABS, polyetherketones, phenolics, polystyrenes,
cellulose, polycarbonates, polyethylenes, polypropylenes, acrylics,
polyurethanes, polyvinyls, polyvinylchlorides, BRICKLITE.RTM., polymeric
and plastic materials well known to those skilled in the art of plastic
materials. Preferably though the carrier plastic or polymer 13 should be
TEFLON.RTM., SILICONE.RTM., or VITON.RTM..
These polymers can be photo, thermally or chemically cured. More
importantly however, they have a molecular structure consisting of long
chains of mostly linear molecules, which after being relaxed by either
controlled heating, dissolution or suspension in a plisticizer or solvent,
provide the interstitial spaces, through which the endothermic or thermal
storage compounds weave and are distributed prior to curing and the final
formation of the PCEA.
(b) The Endothermic Agent.
An endothermic compound or agent is by definition a compound that absorbs
heat. The endothermic agents of the present invention can be strict
endotherms, i.e. they absorb and retain heat without releasing it into the
surrounding environment. Or they can be recyclable endotherms, such as
phase change materials, where they absorb heat initially and then they
release the heat, if they are subjected to an environmental temperature
differential.
The endothermic agents of the present invention comprise the following:
oxidized and unoxidized polymers; oxidized and unoxidized homopolymers of
ethylene polymer compounds; carbon monoxide-bonded copolymers; micronized
polyethylene waxes such as stearic acid; waxes derived from petroleum;
ethylene-bis-stearamide; N,N-ethylene-bis-stearamide; various tars; high
molecular weight oils and hydrocarbons; polyvinyl alcohols; oxidized and
unoxidized polyethylene homopolymers; carnauba wax; aluminum hydroxide,
calcium hydroxide, potassium hydroxide, lithium hydroxide and the mixtures
thereof; boric acid; dodecaborane, paraldehyde, paraformaldehyde, trioxane
and the mixtures thereof; lithium formate, lithium acetate, lithium
carbonate, calcium carbonate, silicon carbonate, magnesium carbonate,
sodium bicarbonate and the mixtures thereof; salts of acetic acid, salts
of formic acid, salts of boric acid and the mixtures thereof; lithium
chloride trihydrate, lithium nitrate trihydrate, sodium carbonate
decahydrate, sodium borate decahydrate, hydrated epsom salts, magnesium
nitrate hexahydrate, beryllium sulfate tetrahydrate, sodium phosphate
dodecahydrate, calcium chloride hexahydrate, zinc sulfate heptahydrate,
magnesium chloride hexahydrate, sodium sulfate decahydrate, aluminum oxide
trihydrate, aluminum sulfate decaoctahydrate, aluminum fluoride trihydrate,
and the mixtures thereof; and any eutectic mixtures of any of these
materials or families of materials including salts with melting points
below 550 degrees Celsius.
These endothermic agents may be micronized and added to the polymer(s)
after said polymer(s) have been relaxed by either controlled heating,
dissolution or suspension in a plasticizer or solvent. The endothermic
agents are then subjected to a mixing process by which they are
distributed through and suspended in the polymer(s)' interstitial spaces,
or in the interstitial spaces of the outer surface of the polymer(s), and
fixed therein through final curing steps which result in the inventive
thermal control composite i.e. the PCEA.
The ultimate effective concentration of the endotherm in the PCEA is
determined on a case by case application basis by such factors as: the
particular application i.e. whether the application requires the
absorption of heat or the release of heat, the needed heat capacity of the
application, the type of polymer used, the particulate size of the
endotherm, and the needed flexibility and use of the novel PCEA. Thus,
when seeking a drapeable PCEA having a thickness of 0.3 to 1.0 mil for a
heat absorbing/heat protective clothing application the carrier plastic or
polymer may be a fluoroelastomer, and the concentration of the endothermic
agent or thermal storage compound may range from 0.0001 to 1.2 grams of
endotherm per square inch of PCEA; with a preferred concentration of 0.01
to 0.06 grams of endotherm per square inch of PCEA.
On the other hand, when seeking a flexible PCEA having an observable
thickness of, for example 1 inch, then the carrier polymer may be a
silicone and the effective concentration of the endotherm in the PCEA will
be 0.05% 60% by weight endotherm in PCEA; with a preferred concentration
of 20% by weight endotherm in PCEA, for extreme maximum flexibility
relative to the highest heat capacity.
The heat absorption/heat protective and/or the heat release/heat
preservation properties of the present inventive PCEA materials become
readily apparent in the Test Examples below, which represent various
embodiments of the inventive PCEAs.
(c) Embodiments of the Invention.
A series of different PCEAs were prepared in accordance with the
principles and requirements as described above. Specifically, natural or
synthetic polymers were selected from the group of polymers set forth
above. These polymers in turn were softened or liquified by (i) heat, (ii)
solution in a solvent or (iii) suspension in a plasticizer, using
conventional methods of softening and liquification already known in the
art of polymer handling and processing.
To these softened or liquified polymers, in turn, were added an
endothermic or a recyclable endothermic agent, preferably micronized,
selected from the group of endotherms or thermal storage compounds set
forth above, in specific concentrations. The polymer and endotherm
combinations were then mixed thoroughly to insure the distribution,
dispersal, and suspension of the endotherms in the polymers's interstitial
spaces; said spaces being formed during the softening of the polymers'
long chains of mostly linear molecules. The mixtures were then molded and
cured into PCEA thin and thick films, PCEA bricks, various shaped PCEA
mulches or extruded, or extruded and spun into PCEA fibers. Alternatively,
the PCEA mixtures were contacted, painted and cured onto a polymer
substrate, so that upon cooling, or evaporation of the solvent or the
plasticizer, the PCEA is literally adsorbed only on the surface of the
underlying polymer substrate.
Claim 1 of 17 Claims
1. A cured flexible thermal
control composite comprising boric acid distributed, dispersed and suspended
in a polymer having a molecular structure consisting of long chains of
mostly linear molecules which prior to curing provide interstitial spaces
through which the boric acid is distributed, dispersed and suspended and
defines a fixed state therein on curing; and a thermally conductive
substrate adhered to said boric-acid containing polymeric material; wherein
said boric acid functions as an endothermic agent to effect heat absorption
at least in part based on liquefaction or decomposition of said boric acid
in said fixed state.
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