U.S. patent number RE34,880 [Application Number 07/638,827] was granted by the patent office on 1995-03-21 for phase change compositions.
This patent grant is currently assigned to The University of Dayton. Invention is credited to Ival O. Salyer.
United States Patent |
RE34,880 |
Salyer |
March 21, 1995 |
**Please see images for:
( Certificate of Correction ) ** |
Phase change compositions
Abstract
Compositions containing crystalline, straight chain, alkyl
hydrocarbons as phase change materials including cementitious
compositions containing the alkyl hydrocarbons neat or in pellets
or granules formed by incorporating the alkyl hydrocarbons in
polymers or rubbers; and polymeric or elastomeric compositions
containing alkyl hydrocarbons.
Inventors: |
Salyer; Ival O. (Dayton,
OH) |
Assignee: |
The University of Dayton
(Dayton, OH)
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Family
ID: |
27417769 |
Appl.
No.: |
07/638,827 |
Filed: |
January 8, 1991 |
Related U.S. Patent Documents
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Application
Number |
Filing Date |
Patent Number |
Issue Date |
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935081 |
Nov 24, 1986 |
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835418 |
Mar 3, 1986 |
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646402 |
Aug 31, 1984 |
4617322 |
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Reissue of: |
88040 |
Aug 19, 1987 |
04797160 |
Jan 10, 1989 |
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Current U.S.
Class: |
106/660; 106/778;
106/802; 106/806; 106/810; 106/18.25; 106/724; 106/696; 106/634;
252/601; 428/920; 428/921; 106/689; 106/18.19 |
Current CPC
Class: |
F28D
20/023 (20130101); C04B 24/00 (20130101); C04B
28/02 (20130101); C04B 41/46 (20130101); C08K
5/01 (20130101); C04B 41/62 (20130101); C04B
28/02 (20130101); C04B 22/06 (20130101); C04B
24/00 (20130101); C04B 24/003 (20130101); C04B
24/005 (20130101); Y02E 60/145 (20130101); C04B
2111/76 (20130101); C04B 2111/00482 (20130101); Y10S
428/921 (20130101); Y02E 60/14 (20130101); C04B
2103/0071 (20130101) |
Current International
Class: |
C04B
41/60 (20060101); C04B 41/62 (20060101); C04B
024/08 () |
Field of
Search: |
;106/634,660,689,696,724,778,802,806,810,18.19,18.25
;428/492,920,921 ;252/601 |
References Cited
[Referenced By]
U.S. Patent Documents
Foreign Patent Documents
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2937712 |
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Aug 1980 |
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DE |
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2087865 |
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Jun 1982 |
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GB |
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Primary Examiner: Green; Anthony
Attorney, Agent or Firm: Killworth, Gottman, Hagan &
Schaeff
Government Interests
GOVERNMENT RIGHTS
The U.S. Government has certain rights under the inventions
disclosed herein.
Parent Case Text
CROSS-REFERENCE TO RELATED APPLICATIONS
This application is a continuation-in-part of U.S. application Ser.
No. 935,081, filed Nov. 24, 1986, now abandoned, which is a
continuation-in-part of U.S. application Ser. No. 835,418, filed
Mar. 3, 1986, now abandoned, which is a continuation-in-part of
U.S. application Ser. No. 646,402, filed Aug. 31, 1984, now U.S.
Pat. No. 4,617,322.
Claims
What is claimed is:
1. A composite useful in thermal energy storage comprising a matrix
having incorporated therein a phase change material, said phase
change material being a crystalline, .[.straight.]. .Iadd.long
.Iaddend.chain, alkyl hydrocarbon having 14 or more carbon atoms
and a heat of fusion greater than 30 cal/g., said composite also
comprising a flame retarding agent selected from the group
consisting of halogenated hydrocarbons and halogenated
phosphates.
2. The composite of claim 1 wherein said matrix material is an
inorganic cementitious material.
3. The composite of claim 2 wherein said inorganic cementitious
material is selected from the group consisting of hydraulic
.[.cements, gypsum, and concrete..]..Iadd.cements and
gypsum..]..Iaddend.
4. The composite of claim 3 wherein said phase change material is
incorporated into said matrix material in the form of a pellet.
5. The composite of claim 4 wherein said pellet comprises a matrix
of a hard wax having a melting point greater than 50.degree. C. and
a penetration hardness less than 10 containing said phase change
material.
6. The composite of claim 3 wherein said phase change material is
pre-mixed with a highly absorptive filler before being introduced
to said matrix material.
7. The composite of claim 1 wherein said flame retarding agent also
includes a polyvalent metal oxide.
8. The composite of claim 2 wherein said composite is formed by
infiltrating said matrix material with said phase change material
in combination a wetting agent.
9. The composite of claim 8 wherein said wetting agent is stearic
acid or stearyl alcohol. .[.10. The composite of claim 1 wherein
said alkyl hydrocarbon is selected from the group consisting of
Shellwax 100, Shellwax 120, Shellwax 200, Shellwax 300, Boron
R-152, Union SR-143, Witco 128, Witco LLN, Witco 45A, Witco K-61,
Witco K-51, Witco 85010-1,
Aristowax 143 and Paraffin 150..]. 11. The composite of claim 2
wherein said alkyl hydrocarbon is a blend of normal alkyl
hydrocarbons containing
16 to 20 carbon atoms. 12. The composite of claim 1 wherein said
halogenated hydrocarbon is selected from the group consisting of
.[.Chlorowax 70-S,.]. tetrabromophthalic anhydride,
tetrabromobisphenol A, and decarbomodiphenyl oxide; and said
polyvalent metal oxide is antimony oxide, the weight ratio of said
halogenated hydrocarbon to said antimony
oxide being about 1:1 to 3:1. 13. A composite of claim 1 wherein
said
composite is a bridge deck. 14. A composite useful in thermal
energy storage comprising a matrix material having incorporated
therein a phase change material, said matrix material being
plasterboard and said phase change material being a crystalline,
.[.straight.]. .Iadd.long .Iaddend.chain, alkyl hydrocarbon having
14 or more carbon atoms and a heat of fusion greater than 30
cal/g., said plasterboard also comprising a flane retardant agent
incorporated therein said flame retarding agent being selected from
the group consisting halogenated hydrocarbons and
halogenated phosphates. 15. A composite useful in thermal energy
storage comprising a matrix material having incorporated therein a
phase change material and a flame retarding agent, said phase
change material being a crystalline .[.straight.]. .Iadd.long
.Iaddend.chain alkyl hydrocarbon having 14 or more carbon atoms and
a heat of fusion greater than 30 cal/g and said flame retarding
agent being a brominated hydrocarbon which is
miscible in said phase change material. 16. The composite of claim
15 wherein said brominated hydrocarbon is a brominated
cycloalkylalkanes.
The composite of claim 16 wherein said brominated cycloalkylalkane
is
dibromoethyldibromocyclohexane. 18. The composite of claim 1
wherein said flame retarding agent is a flame retarding agent
selected from the group consisting of tri(beta-chloroisopropyl)
phosphate and
tri(beta-chloroethyl)phosphate. .Iadd.19. A method of thermal
energy storage comprising providing a composite in thermally stable
form and formed of a first material and a second material which is
different from said first material, and which has a melting point
less than said first material, but which is compatible with said
first material, said first material comprising an inorganic
cementitious matrix which serves as a containment means for said
second material, said second material comprising a crystalline
alkyl hydrocarbon material containing 14 or more carbon atoms or
mixtures thereof and having a heat of fusion greater than about 30
cal/g, said second material being contained within the matrix of
said first material, and subjecting said composite to changes in
temperature whereby said composite either conserves heat or
cool.
.Iaddend. .Iadd.20. The method of claim 19 wherein said inorganic
cementitious matrix comprises a cementitious material selected from
the group consisting of hydraulic cements and gypsum. .Iaddend.
.Iadd.21. The method of claim 20 wherein said inorganic
cementitious matrix is in the form of a dry wall or a cured cement
product. .Iaddend. .Iadd.22. The method of claim 21 wherein said
composite is formed by infiltrating said inorganic cementitious
matrix with neat crystalline alkyl hydrocarbon. .Iaddend. .Iadd.23.
The method of claim 23 wherein said crystalline alkyl hydrocarbon
is used in combination with a wetting agent. .Iaddend. .Iadd.24.
The method of claim 20 wherein neat crystalline alkyl hydrocarbon
is incorporated directly into said inorganic cementitious matrix by
wet or dry mixing. .Iaddend. .Iadd.25. The method of claim 25
wherein said crystalline alkyl hydrocarbon is used in combination
with a
wetting agent. .Iaddend. .Iadd.26. The method of claim 19 wherein
said phase change material comprises from 1 % to 20% by weight of
said composition. .Iaddend.
Description
BACKGROUND OF THE INVENTION
The present invention relates to compositions embodying phase
change materials and, more particularly, to compositions containing
crystalline, long chain alkyl hydrocarbons having at least 14
carbon atoms.
There is a great deal of interest in phase change thermal energy
storage systems due to their inherent ability to store large
amounts of heat and release it to the surrounding environment as
temperatures drop below or exceed predetermined levels. These
systems are of particular interest in the architectural and
building trades where climate control and its concomitant energy
consumption is one of the principal considerations in building
design and material selection.
A variety of building materials and techniques have previously been
used to conserve heat or cool and thereby reduce energy costs.
Included among them are structural elements which incorporate phase
change materials. By incorporating phase change materials into
building materials, energy in excess of that necessary to maintain
comfort conditions is inherently absorbed and released as required
to maintain the comfort range. Thus, in winter months, phase change
materials incorporated into structural elements in the walls or
floors of buildings and the like can absorb solar energy during
daytime hours and release it to the interior at night as
temperatures drop. In summer months, the same phase change
material, due to its thermostatic character, conserves coolness by
absorbing energy.
Structural elements incorporating phase change materials are more
desirable than elements which store only sensible heat because they
have a higher capacity to store energy and they absorb and release
a large quantum of energy over a very narrow temperature range. A
phase change material utilizes its latent heat of fusion as well as
its sensible heat capacity for thermal storage. The latent heat of
fusion is substantially greater than the sensible heat capacity of
the material. That is, the amount of energy a material absorbs upon
melting, or releases upon freezing, is much greater than the amount
of energy it absorbs or releases upon increasing or decreasing in
temperature 1.degree. C. Thus, upon melting and freezing, per unit
weight, a phase change material absorbs and releases substantially
more energy than a sensible heat storage material which is heated
or cooled through the same temperature range. Furthermore, as
contrasted with a sensible heat storage material which absorbs and
releases energy essentially uniformly over a broad temperature
range, a phase change material absorbs and releases a large quantum
of energy in the vicinity of its melting/freezing point. This is
particularly advantageous in buildings where space is at a premium
and energy storage and release are required within a very narrow
comfort range.
It has long been recognized that an effective phase change
material, which could store and release thermal energy within the
temperature range of 10.degree.-65.degree. C. and could be
economically incorporated into common building materials (e.g.
concrete, cement, plaster, rubber, plastics), would have broad
utility for many heating and cooling applications including solar
passive, solar active, off-peak electric load leveling, bridge deck
deicing, etc. Other types of phase change materials have been
investigated that melt and freeze in the above temperature range,
and have a high heat of fusion (e.g., salt hydrates and
clathrates); but widespread use has not been achieved because of
the difficulty of containerizing them, their instability to
repeated thermocycling, corrosion, leakage, etc.
Paraffin waxes have been considered for use in building materials
as phase change materials but until now effective methods of
incorporating them into building materials were not available
and/or they involved prohibitive loss in the physical properties of
the building materials.
Among the teachings which were available in the art prior to the
present invention are those of U.S. Pat. No. 4,259,401 to Chahroudi
et al which discloses both structural and non-structural building
materials incorporating phase change materials. These building
materials are made up of a rigid porous matrix structure which is
impregnated with the phase change material. Three classes of phase
change materials are disclosed, namely, hydrated salts, waxes, and
clathrates. Cements, plasters or thermosetting materials may form
the rigid matrix.
U.S. Pat. No. 4,504,402 to Chen teaches an encapsulated phase
change material which is prepared by forming a shell about a phase
change composition in compacted powder form. One of the
applications of the encapsulated phase change materials is in
concrete or gypsum structures.
SUMMARY OF THE INVENTION
The present invention is broadly directed to compositions which are
useful in thermal energy storage and include crystalline, long
chain, alkyl hydrocarbons having 14 or more carbon atoms, as phase
change materials.
Crystalline alkyl hydrocarbon are particularly advantageous phase
change materials. The melting temperature of the paraffins
increases until a "limiting" melting point of about 130.degree. C.
is reached in products having more than 40 carbon atoms in an
unbranched chain. Consequently, one can select a crystalline
hydrocarbon of any desired melting temperature between 0.degree.
and 80.degree. C. for use as a phase change material for solar
active and passive applications. Depending on the purity of the
compounds, heats of fusion range from about 40 to 60 cal/gm. The
compounds are non-toxic, non-corrosive and non-hygroscopic and
inexpensive. At the same time, they are fairly resistant to thermal
cycling.
It has been found that alkyl hydrocarbons are particularly useful
in the form of blends of two or more crystalline alkyl
hydrocarbons. More particularly, it has been found that crystalline
alkyl hydrocarbon blends obtained at low cost as byproducts of
petroleum refining operations are economically advantageous for use
in the present invention. Depending on the difference in the
melting points of the constituents of the blend, the blend exhibits
thermal storage characteristics intermediate those of the
individual alkyl hydrocarbons without a decrease in heat of
fusion.
By choosing the proper alkyl hydrocarbons, the temperature at which
thermal energy is stored can be varied from -12.degree. C.
(tetradecane) to 95.degree. C. (commercial microcrystalline waxes).
For bridge deck deicing, hexadecane, which melts at about
10.degree. C., is advantageous. For solar passive applications in
climate control octadecane, which melts at about 28.degree. C., is
used. For solar active storage applications commercial paraffin
waxes which melt in the range of 50.degree.-65.degree. C. are
desirable.
In accordance with one embodiment of the present invention,
crystalline, alkyl hydrocarbons are incorporated into polymeric or
inorganic cementitious compositions such as hydraulic cements.
It has been found that alkyl hydrocarbons can be directly
incorporated, by dry or wet mixing, into hydraulic cementitious
compositions such as concrete, cement and plaster, at
concentrations up to 10 percent by weight in the case of certain
cements and 10 to 20 percent by weight in the case of gypsum,
without prohibitive loss in the strength properties of the matrix.
In accordance with more preferred embodiments of the invention
alkyl hydrocarbons are pre-mixed with an absorptive filler or
incorporated into a hard wax, or rubber or plastic pellet, for
incorporation into inorganic cementitious mixes.
In accordance with another embodiment of the present invention,
certain flame-resistant agents are used in combination with the
crystalline alkyl hydrocarbons to confer flame retardancy. Certain
halogenated hydrocarbons are useful for this purpose. These
hydrocarbons are preferably used with a polyvalent metal oxide such
antimony oxide, which reacts with the halogen liberated upon
combustion and generates a dense snuffing gas.
In another embodiment of the invention, the alkyl hydrocarbons are
permeated into inorganic cementitious compositions in combination
with a polar hydrocarbon such as stearyl alcohol which functions
similar to a wetting agent by enhancing the affinity of the
hydrocarbon for the cement and enabling the hydrocarbon to permeate
a clay or cement body. In this embodiment, the alkyl hydrocarbon
not only conveys its thermal storage capacity to the body but may
also water-proof it.
In accordance with another embodiment of the invention, the alkyl
hydrocarbon is incorporated into plastic or rubber carriers, with
or without crosslinking. These composites can be incorporated as
granules or pellets into hydraulic cementitious products or used to
make floor tiles, wall coverings and the like. Additional thermal
storage capacity is gained using crystalline rubber carriers that
melt in the same or a different temperature range as the alkyl
hydrocarbons and exhibit a significant heat of fusion.
A further embodiment of the present invention resides in polymeric
compositions and, more particularly, elastomeric compositions
containing crystalline alkyl hydrocarbon useful in forming
moldings, sheets, films, rods, fibers, as well as pellets. These
compositions can be designed to be useful in the manufacture of
flooring, tiles and wall panels having excellent thermal storage
capability.
BRIEF DESCRIPTION OF THE DRAWINGS
The present invention will be explained by reference to the
accompanying drawings wherein:
FIG. 1 is a differential scanning calorimetry curve for the
cementitious composition of Example 1.
FIG. 2 is a differential scanning calorimetry curve for the
polymeric composition of Example 2.
DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS
In accordance with the present invention, crystalline alkyl
hydrocarbons containing 14 or more carbon atoms are incorporated
into matrix materials where they function as phase change
materials.
A number of commercially available waxes with melting points up to
about 95.degree. C. are useful as phase change materials in the
present invention including Shellwax 100 (mp 42.degree.-44.degree.
C.), Shellwax 120 (mp 44.degree.-47.degree. C.), Shellwax 200 (mp
52.degree.-55.degree. C.), Shellwax 300 (mp 60.degree.-65.degree.
C.), Boron R-152 (mp 65.degree. C.), Union SR-143 (mp about
61.degree. C.), Witco 128 (mp about 53.degree. C.), Witco LLN (mp
40.degree. C.), Witco 45A (mp 31.degree. C.), Witco K-61 (mp
24.degree. C.), Witco K-051 (mp 17.degree. C.,), Witco 85010-1 (mp
7.degree. C.), Aristowax 143 (mp 34.degree.-61.degree. C.), and
Paraffin 150 (mp about 61.degree. C.). These waxes have heats of
fusion greater than 30 cal/g and, by comparison to other phase
change materials, they are inexpensive--many of them costing as
little as 28 U.S. cents per pound when purchased in tank car
quantities. The waxes can be used alone or in combination. For
example, higher melting commercial paraffin waxes such as Shell 100
(mp 42.degree. C.), Shellwax 120 (mp 44.degree.-47.degree. C.),
Shellwax 200 (mp 52.degree.-55.degree. C.), Witco 128 (mp
53.degree. C.), Paraffin 150 (mp 61.degree. C.), can be blended
with lower melting C.sub.16 (mp 10.degree. C.) and C.sub.18 (mp
28.degree. C.) crystalline hydrocarbons to produce phase change
materials with intermediate melting temperatures and these can be
incorporated into structures materials as described above.
A preferred group of waxes for use in the present invention are
mixtures of crystalline alkyl hydrocarbons in which the melting
points of the individual constitutents fall within a range of about
0.degree. to 95.degree. C. and more preferably 5.degree. to
60.degree. C. If the difference in melting points of the waxes
making up the mixture is greater than about 20.degree. C. the blend
will exhibit two distinct melting points and, hence, possess two
heats of fusion.
A particularly preferred class of waxes useful in the present
invention contain a blend of alkyl hydrocarbons and are obtained at
low cost as byproducts of petroleum refining. Because they are
inexpensive, they can be incorporated into building materials at
minimal additional expense and, at the same time, provide high
savings in terms of reduced energy costs. The preferred blends for
passive heating have a melting point in the range of 24.degree. to
32.degree. C. Preferred blends for passive cool store have a
melting point in the range of 28.degree. to 24.degree. C. In many
applications, the blends will be relied upon for heating and
cooling. A blend melting and freezing at 23.degree. to 25.degree.
C. can be used as a thermal mass throughout a building for heating
and cooling. A particularly preferred blend is available from Witco
Chemical Corporation under the designation K-61. This wax has a
melting point of 24.degree. C. and a freezing point of 19.8.degree.
C. (by differential scanning calorimetry at 10.degree. C./min. rate
of heating and cooling). Chromatographic analysis of K-61 shows
that it principally contains normal paraffins of 16 to 21 carbon
atoms with major fractions consisting of 17, 18, 19 and 20 carbon
atoms.
Thermal energy storage data for five products obtained from Witco
Chemical Corporation are shown in the following table which shows
that blends having melting and freezing temperatures which cover
the enire range that is deemed to be of interest for solar passive
heating and cooling are available.
______________________________________ Tm Tc Tm-Tc Hf Hc .degree.C.
.degree.C. .degree.C. cal/gm cal/gm
______________________________________ 1. WITCO LLN 40.0 34.7 5.3
51.1 49.2 2. WITCO 45-A 31.4 26.3 5.1 41.2 40.0 3. WTTCO K-61 24.0
19.8 5.2 48.4 47.8 4. WITCO K-51 17.4 12.3 5.1 47.6 11.2 5. WITCO
85010-1 7.6 4.0 3.6 30.4 31.0
______________________________________
Another important consideration in the selection of the alkyl
hydrocarbons used in the present invention is their tendency for
supercooling or superheating. It is desirable to use alkyl
hydrocarbons which show little or no supercooling even when cooled
at rapid rates such as 10.degree. C./min. In any case, the
difference in observed melting and freezing temperatures due to
supercooling or superheating is preferably less than 10.degree. C.
More preferably this difference is less than 5.degree. C. and most
preferably less than about 3.degree. C.
In addition to providing blends of alkyl hydrocarbons which exhibit
phase change characteristics which are intermediate or
approximately the average of the individual phase change materials
making up the blend, it is also possible to provide blends which
exhibit two or more distinct phase changes. Such blends are useful
in applications where the phase change material is relied upon to
conserve heat in the winter and consume cool in the summer. For
this embodiment of the invention the difference in the melting
points of the phase change materials should be at least 15.degree.
C. Typical examples of such dual temperatures blends is a blend
which freezes at 15.degree. C. and melts at 35.degree. C. on
heating. Many waxes, as commercially obtained, are not preferred
for use in passive energy storage systems as used in climate
control because their melting point is too high. Consequently, in
accordance with the invention, these materials may be combined with
crystalline alkyl hydrocarbons having 14-18 carbon atoms and, more
specifically, 14, 16, or 18 carbon atoms in order to bring the
melting point of the blend within the range of 16.degree. to
42.degree. C.
Stearic acid esters are also useful phase change materials.
Examples of useful stearic acid esters include methyl stearate,
ethyl stearate, propyl stearate, butyl stearate, etc. Butyl
stearate changes phase sharply at about 23.degree. C. and can be
permeated into crosslinked polyolefins and percolated into
plasterboard.
A particularly desirable embodiment of the present invention
utilizes flame-resistant halogenated hydrocarbons and, more
particularly, flame-resistant crystalline chlorinated hydrocarbons
for flame retardancy. Typical examples of flame-resistant
hydrocarbons are halogenated hydrocarbons such as chlorinated,
brominated or fluorinated hydrocarbons. Representative examples
include Chlorowax 80S, available from Diamond Shamrock Corp. Other
halogenated hydrocarbon (which are not phase change materials) can
also be used, several of which are available from Ethyl
Corporation. Included among them are tetrabromophthalic anhydride,
tetrabromobisphenol A, and decabromodiphenyl oxide.
A particularly useful flame-resistant hydrocarbon is a brominated
hydrocarbon which is miscible in the phase change material.
Miscibility is particularly important when permeating the
flame-resistant hydrocarbon into already formed plasterboard along
with the phase change material. Examples of brominated hydrocarbons
which are miscible in the phase change material are brominated
alkanes, and more particularly, brominated cycloalkylalkanes such
as dibromoethyldibromocyclohexane which is available as Saytex
BCL-462 from the Ethyl Corporation.
The flame resistant hydrocarbon is preferably incorporated into the
phase change material in a concentration which provides a
self-extinguishing product. In the case of Saytex BCL-462amounts as
low as 10% by weight based on the phase change material are
sufficient for this purpose.
Halogenated hydrocarbons are preferably used in combination with
conventional flame-resistant fillers such as antimony oxide and
other polyvalent metal oxides. The weight ratio of halogenated
hydrocarbon to oxide may vary, but it is typically about 1:1 to
3:1. Flame-resistant wax formulations have previously been added to
polymers to render them self-extinguishing. Wax formulations used
for this purpose may also be useful as flame-resistant phase change
materials in accordance with the present invention.
Another useful fire retardant is a halogenated phosphate.
Particularly useful flame-resistant halogenated phosphates are
chlorinated phosphates such as tri(beta-chloroisopropyl) phosphate
which is commercially available under the designation FYROL PCF
from Staffer Chemical Company, Specialty Chemical Division and
tri(beta-chloroethyl)phosphate which is commercially available
under the designation PHOSGARD C-22R from Monsanto Chemical
Company. Although insoluble in the phase change material,
tri(beta-chloroisopropyl) phosphate can be dispersed in the phase
change material.
It has been found that alkyl hydrocarbons are compatible with both
cementitious and polymeric materials and, as such, they can be
incorporated into these materials and used in the building trade to
provide structures having desirable thermal energy storage
characteristics.
The inorganic cementitious compositions of the present invention
include an inorganic cementitious material as a rigid
matrix-forming material Typical examples of useful cementitious
materials are hydraulic cements, gypsum, plaster of Paris, lime,
etc. Portland cement is by far the most widely hydraulic cement.
Portland cements are ordinarily used for construction purposes.
Types I, II, III, IV, and V may be used. White cements, air
entrained cements, high alumina cements, masonry cements can also
be used.
Concretes are mixtures of hydraulic cements and aggregates. Typical
aggregates include coarse aggregates such as gravel, granite,
limestone, quartz, etc., as well as so-called fine aggregates such
as sand and fly ash. Conventional hydraulic cement concretes, e.g.,
Portand cement concretes, employ major amounts (e.g., about 50 to
75% by volume) of such aggregates in the set product. These cements
and concretes fall within the term "inorganic cementitious
material" as it is used herein.
The inorganic cementitious compositions of the present invention
also include concrete and plaster compositions useful in the
manufacture of pre-formed materials such as concrete blocks, dry
wall, and the like as well as in forming poured concrete structures
such as used in forming the walls, floors, floor pads and
partitions of buildings. In addition, the compositions of the
present invention also include compositions useful in road, runway
and bridge deck construction where icing can be prevented by
incorporation of the phase change material for thermal energy
storage during the day, and release during the night to prevent
freezing of water on the surface.
Alkyl hydrocarbons can be incorporated into inorganic cementitious
compositions directly by blending the hydrocarbon with the other
components of the cement or concrete prior to shaping the
compositions and allowing them to harden. Another method that can
be used to great advantage is to permeate pre-formed and hardened
porous building materials with the alkyl hydrocarbons. Various
concrete, stone-like, or clay based on elements such as dry wall,
cured cement products, bricks, and concrete blocks can be permeated
with an alkyl hydrocarbon in this manner.
Infiltration is especially adapted for retrofitting applications.
To infiltrate pre-formed building materials it is generally
necessary to heat the material to a temperature in excess of the
melting point of the alkyl hydrocarbon. Of course, in some
applications it may not be necessary to actually penetrate the
underlying substrate with the alkyl hydrocarbon. Rather, the alkyl
hydrocarbon composition can simply be coated on the surface layer
of the substrate such that it penetrates into the surface.
The infiltration with C-18 alkyl hydrocarbon can be used to treat
and saltproof, existing highway bridge decks or airport runways to
prevent the deterioration caused by salt-induced corrosion of the
bridge's reinforcing steel rods. If the alkyl hydrocarbon is
selected to melt and freeze just above 0.degree. C., the safety
hazard, in the snow belt, where the bridge deck freezes before the
rest of the highway can simultaneously be reduced or
eliminated.
When incorporated into inorganic cementitious compositions by
direct blending or by permeation, the alkyl hydrocarbons are
preferably used in combination with a polar hydrocarbon which
functions similar to a wetting agent by enhancing the affinity of
the alkyl hydrocarbon for the cement and/or lowering its surface
tension. In this case the alkyl hydrocarbon permeates the concrete
and, in addition to functioning as a phase change material, also
functions in waterproofing the concrete.
Representative examples of useful polar hydrocarbons include long
chain (i.e., having more than 12 carbon atoms) fatty acids and
alcohols such as stearic acid, stearyl alcohol and poor waxes such
as montan wax or hydrogenated tallow. The polar hydrocarbon used is
also a phase change material and thus may be used in amounts up to
100 parts per 100 parts of alkyl hydrocarbon and preferably about 1
to 25 parts per 100 parts alkyl hydrocarbon. The alkyl hydrocarbon
migrates throughout the concrete, and to the surface whereby it
seals the concrete and renders it waterproof.
It has been found that directly incorporating alkyl hydrocarbons
into cement or concrete compositions prior to hardening tends to
reduce the strength (not the setting time) of the set concrete. The
alkyl hydrocarbon is lubricative and reduces the amount of adhesion
of the cement to the sand and aggregate that can occur in the
concrete matrix. It is generally not desirable to use more than
about 5% dry weight alkyl hydrocarbon in a concrete composition.
However, if the amount of aggregate in the composition is reduced
or the aggregate is completely eliminated, approximately 10% alkyl
hydrocarbon may be added. On the other hand, in gypsum, plaster of
paris, or dry wall compositions, between 10 and 20% by weight of
the alkyl hydrocarbon may be added in the wet mix.
It has also been found that the amount of alkyl hydrocarbon
incorporated into inorganic cementitious compositions such as
Portland cement compositions and the like can also be increased if
the alkyl hydrocarbon is used in combination with a highly
absorptive filler such as a finely divided silica (e.g., CAB-O-SIL
or HiSil). It has been found that pre-mixing the alkyl hydrocarbon
with such a highly absorptive filler, the hydrocarbon resides in
the filler and detracts less from the strength of the concrete or
cement composition.
There is no lower limit on the amount of alkyl hydrocarbon used in
the composition since theoretically any amount will provide some
thermal storage benefit. Typically, the compositions of the present
invention contain at least 1% of the crystalline alkyl
hydrocarbon.
As previously disclosed, the alkyl hydrocarbons maybe used in
combination with other halogenated hydrocarbons and a polyvalent
metal oxide to impart flame retardancy to the composition. If the
polyvalent metal oxide is mixed directly with the alkyl hydrocarbon
and permeated into a concrete block, brick, or the like, the porous
network of the block often strains the oxide from the wax
composition. Consequently, when infiltration concrete and clay
structures with alkyl hydrocarbons, it has been found desirable to
pre-mix metal oxide with the concrete composition and to permeate
the hardened concrete product with the halogenated wax-containing
alkyl hydrocarbon.
Because there is a tendency for alkyl hydrocarbons to detract from
the physical properties of set concrete compositions, it may be
desirable to incorporate the hydrocarbon in the cement compositions
in one of the polymeric or wax compositions described below in the
form of a pellet or granule ranging from about 0.25 to 3.0 mm in
particle size.
Pellets or granules can be produced by incorporating the alkyl
hydrocarbon in a polymer, and grinding or cutting the polymer. For
use in cementitious compositions, the polymeric compositions need
not be cross-linked since the thermal form stability of the pellet
is not important. In this case, the cementitious composition can
include up to 50% by weight of the pellets or granule containing
the hydrocarbon phase change material. To increase the amount of
alkyl hydrocarbon incorporated or imbibed into the pellet and to
hold it in the pellet it is often desirable to include the
aforementioned absorptive silica filler in the pellet.
In accordance with one embodiment of the invention, pellets are
formed using hard waxes instead of polymers. The waxes may be
crystalline or non-crystalline. When they are crystalline,
depending upon the conditions at which they are used, their heat of
fusion may contribute to the thermal storage characteristics of the
pellet. This is particularly useful in active thermal energy
storage where higher temperatures are used.
Representative examples of hard waxes which are useful in the
present invention include Shellwax 300, a product of Shell Oil
Company, Chlorowax 70S, stearic acid, and high melting
mcirocrystalline waxes (e.g., Petrolite waxes available from Barco
Products). These waxes are characterized in that they have a
melting point greater than 50.degree. C. and a penetration hardness
as measured by ASTM D 1321-61T less than about 10.
The cementitious compositions of the present invention can be
designed for use in various passive thermal storage applications by
appropriately selecting the melting point of the alkyl
hydrocarbons. Alkyl hydrocarbons which melt in the range of about
16.degree. to 42.degree. C. are used in passive solar heating such
as in the building materials and structures previously mentioned.
For bridge deck or roadway deicing, alkyl hydrocarbons which melt
at about 5.degree. to 15.degree. C. are preferably used.
In accordance with the present invention, alkyl hydrocarbons can
also be incorporated into thermosetting or thermoplastic,
elastomeric or non-elastomeric polymeric materials to form wall
coverings, floor coverings or the aforementioned pellets. Included
within the scope of the term "polymeric materials" are natural and
synthetic rubbers. The polymeric material must be compatible with
the alkyl hydrocarbons such that the alkyl hydrocarbon can be
incorporated into the polymeric material and remain dispersed
therein upon molding or coating. If the materials are not
sufficiently compatible, the alkyl hydrocarbon will be more
difficult to disperse in the polymer and will be present as
dissolved phase and as a phase of dispersed droplets. Whether the
alkyl hydrocarbon is dissolved or dispersed does not appear to have
a significant effect on the melting and crystallization of the
phase change material.
Crystalline long chain hydrocarbons can be most readily dispersed
in less polar or non-polar rubbers or polymers such as natural
rubber, butyl rubber, polybutadiene, copoly(butadiene/styrene) and
copoly(ethylene/propylene) (EPDM). They can also be dispersed in
polar polymers such as nylons, polyesters, acrylate rubbers,
methacrylate rubbers, polyvinl alcohol, ethylene vinylacetate
copolymers, polyvinyl acetate, vinyl chloride/vinyl acetate
copolymer, Neoprene, butadiene-acrylonitrile rubber, etc. It is
also desirable to use flame resistant halogenated polymers such as
Neoprene, polyvinyl chloride, and polyvinylidene chloride.
The polymeric compositions of the present invention can be used in
a crosslinked or uncrosslinked form depending one end use and the
need for thermal form stability. Crosslinking does not necessarily
interfere with the phase change properties of the crystalline alkyl
hydrocarbon. However, it is essential that the polymer compositions
not be crosslinked to an extent that the phase change material
loses its ability to melt and freeze effectively and results in
reduced least of fusion.
It is particularly advantageous to incorporate the alkyl
hydrocarbon into rubbers and other elastomers having significant
crystallinity so that they can also function as phase change
materials. Natural rubber reportedly has phase transitions at
-6.degree. and 25.degree. C. Neoprene (polychloroprene) reportedly
has a crystalline melting point about 32.degree. C., as is
desirable for comfort heating. Other semi-crystalline rubbers
include some EPDM, and copoly- (ethylene/vinyl acetate) rubbers.
Hence, a crystalline matrix rubber containing an alkyl hydrocarbon
can provide augmented thermal energy storage capacity since both
parts of the composite contribute.
The alkyl hydrocarbon can be incorporated into the aforesaid
polymeric compositions in amounts of up to 50% by weight, depending
on the nature of the hydrocarbon and the polymer used.
Theoretically, there is no lower limit on the amount of phase
change that is used since some thermal energy storage benefit
(although small) accompanies any addition. Usually, the phase
change material is used in an amount of at least 1% by weight.
In forming molded products, the alkyl hydrocarbon can be mixed with
the polymeric material in a conventional manner, e.g., in a Banbury
or on a roll mill. Furthermore, conventional plasticizers, fillers,
pigments, curing agents, accelerators, etc., can be added to the
compositions to adjust their physical properties as desired. It is
advantageous to add fillers such as finely divided silica and
carbon black to the polymer composition. They may be added in
amounts ranging from about 10 to 100 parts per 100 parts of
polymer.
The polymeric compositions of the present invention can be
compounded in an otherwise conventional manner to provide
compositions useful in forming rubber floor tiles, flooring and the
like.
In accordance with another embodiment of the invention, polymeric
thermoset foams such as polyurethane, or thermoplastic polystyrene
foams useful in insulation and other applications may be filled
with an alkyl hydrocarbon to enhance their insulative capacity in
accordance with the present invention. Flexible open celled foams
can be filled with an alkyl hydrocarbon by compressing the foam in
a melt of the hydrocarbon, and removing the excess by
re-compressing the foam after removing it from the melt. Preferred
foams are flexible, low density, open cell foams; however,
substantially any foam in which enhanced thermal storage
characteristics are desired can be impregnated with a phase change
material in accordance with the present invention.
In accordance with still another embodiment of the invention,
pellets formed in accordance with the present invention are used in
active or passive hybrid thermal storage systems such as pellet bed
heat exchanger in which a heat exchange fluid such as air, ethylene
glycol, water or the like is circulated through a pellet bed. In
this use the pellets (the carrier polymer) are preferably
crosslinked and the alkyl hydrocarbon has a melting point in the
range of 10.degree. to 65.degree. C. In one embodiment of the
invention black pellets (e.g., containing carbon black filler) can
be formed and used as a combination collector and storage unit.
These pellets can be used in solar water heaters where they absorb
sunlight and store energy. In this embodiment a phase change
material having a melting point of about 140.degree. F. is used.
Similarly, pellets formed in accordance with the invention can be
used in a coffee or tea cup to keep the drink warm.
A partial listing of building materials which can be modified to
incorporate alkyl hydrocarbons as phase change materials in
accordance with the present invention includes plasterboard,
plaster, cement blocks, cement stucco, cement floors, plastic and
rubber floor tiles, foams insulation and paints.
The present invention is illustrated in more detail by reference to
the following examples.
EXAMPLE 1
A cementitious phase change composition was prepared by adding
octadecane to an aqueous slurry of gypsum in an amount of 10 parts
octadecane per 90 parts gypsum. The composition was allowed to
harden and submitted to differential scanning calorimetry (DSC)
analysis. The temperature scan rate was 10.degree. C. per minute.
The DSC curve is shown in FIG. 1. The figure clearly shows the
melting (32.2.degree. C.) and crystallization (27.4.degree. C.) of
octadecane. Thus, the C-18 alkyl hydrocarbon retains its
advantageous latent heat storage characteristics in gypsum.
EXAMPLE 2
A rubber composition useful in forming sheets or pellets for
passive thermal storage was prepared by compounding 100 parts
natural rubber, 100 parts octadecane, 1 part stearic acid, 40 parts
Cabosil, 2.0 parts Santecure NS, 5.0 parts zinc oxide, 2.5 parts
Flexzone, and 2.5 parts sulfur. The composition was cured at
350.degree. F. for 30 minutes and submitted to DSC analysis. The
DSC curve at a temperature scan rate of 10.degree. C./Min. is shown
in FIG. 2. Melting and crystallization of the octadecane occurred
at 25.8.degree. C. and 18.2.degree. C., respectively. The heat of
fusion of the octadecane was thus retained.
EXAMPLE 3
The follwing rubber (EPDM) compositions were prepared and cured at
350.degree. F. for 30 minutes. The alkyl hydrocarbons employed in
each of the compositions retained their melting point and heat of
fusion characteristics.
______________________________________ Parts by Weight 1 3 7 5 9 11
______________________________________ EPDM 100 100 100 100 100 100
Shell X-100 Paraffin 66 66 50 33 33 33 Wax (Shell Oil Co.) Silica
Filler 50 -- 50 50 -- -- Carbon Black Filler -- 50 -- -- 50 50
Stearic Acid 5 5 5 5 5 5 DiCup R (Hercules 3 3 3 3 3 3 Chemical
Co., vulcan- izing agent) Octadecane -- -- 16 33 -- -- Octadecane
(technical -- -- -- -- 33 -- grade) Hexadecane -- -- -- -- -- 33
______________________________________
EXAMPLE 4
Twelve 2".times.2" squares of plasterboard were dried in a vacuum
dessicator overnight and then weighed and labeled. Separate melt
mixed percolating baths were prepared containing
LLN/BCL-462/stearic acid in the ratios of 85/10/5, 80/15/5 and
75/20/5. Another series was prepared using 45A/BCL-462 /stearic
acid in the same ratios. The blends were weighed into metal beakers
and heated to 80.degree. C. Duplicate plasterboard samples were
immersed in each blend for ten minutes. After ten minutes in the
bath, the samples were immediately removed and weighed to calculate
the percent phase change material (PCM) absorbed which is listed in
Table 1 for each sample.
TABLE I ______________________________________ WITCO
45A/BCL-462/STEARIC ACID PICKUP IN PLASTERBOARD PERCOLATED WITH THE
FIRE RETARDANT POSITIONS Dry Weight Final Sample # Ratio % PCM
Pickup ______________________________________ 45 A/BCL 462/Stearic
Acid 1 85/10/5 33.8 2 85/10/5 34.13 3 80/15/5 35.08 4 80/15/5 34.09
5 75/20/5 33.91 6 75/20/5 33.02 Control 1 95/0/5 32.99 Control 2
95/0/5 32.75 LLN/BCL 462/Stearic Acid 7 85/10/5 34.38 8 85/10/5
34.02 9 80/15/5 34.80 10 80/15/5 34.69 11 75/20/5 34.96 12 75/20/5
34.22 Control 1 95/0/5 35.75 Control 2 95/0/5 34.96
______________________________________
The paper cover was completely removed from one of the squares in
each group. Each sample was mounted horizontally in a hood and
ignited for ten seconds with a Bunsen burner. Table 2 is a
compilation of the fire retardant test data.
TABLE 2
__________________________________________________________________________
FIRE RETARDANCE TESTS OF PERCOLATED PLASTERBOARD Ignite in Time to
Time to Ignite Flame Time to Sample # Ratio 10 sec Extinguish and
Stay Lit Traveled Extinguish Smoke
__________________________________________________________________________
45A/BCL 462/Stearic Acid 1 85/10/5 Yes Immed. 30 sec Yes 375 sec wh
& blk 2 85/10/5 Yes Immed. 29 Yes 390 wh & blk 3 80/15/5
Yes Immed. 26 Yes 341 wh & blk 4 80/15/5 Yes Immed. 25 Yes 201
wh & blk 5 75/20/5 Yes Immed. 30 Yes 160 wh & blk 6 75/20/5
Yes Immed. 30 Yes 130 wh & blk Control 1 95/0/5 Yes 10 min. 10
Yes 10 min. wh & blk Control 2 95/0/5 Yes 10 min. 10 Yes 10
min. wh & blk LLN/BCL 462/Stearic Acid 7 85/10/5 Yes Immed. 12
sec Yes 323 sec wh & blk 8 85/10/5 No Immed. 15 Yes 272 wh
& blk 9 80/15/5 Yes Immed. 20 Yes 237 wh & blk 10 80/15/5
No Immed. 25 Yes 196 wh & blk 11 75/20/5 Yes Immed. 30 Yes 155
wh & blk 12 75/20/5 No Immed. 36 Yes 58 wh & blk Control 1
95/0/5 Yes 10 min. 10 Yes 10 min. wh & blk Control 2 95/0/5 Yes
10 min 10 Yes 10 min. wh & blk
__________________________________________________________________________
NOTE Evennumbered samples had paper covers removed
Controls were included containing LLN/stearic acid and 45A/stearic
acid in the ration of 95/5.
Having described the invention in detail and by reference to
specific embodiments thereof, it will be apparent that numerous
modifications and variation are possible without departing from the
scope of the following claims.
* * * * *