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Description  |
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INTRODUCTION
The present invention is directed to heating devices having uses such as
taught in Cambridge, U.S. Pat. No. 3,314,413; Glasser, U.S. Pat. No.
3,301,250; Staples, U.S. Pat. No. 3,906,926; and Chapin, U.S. Pat. No.
3,924,603. All of these patents teach so-called "flameless" heating
devices, generally in the form of blankets that may be laid against an
object to be heated and then activated, as by addition of water. While
each of the prior devices has a certain utility, they all suffer from one
or more important disadvantages: lack of control over heat production;
insufficient length in the heating cycle; inadequate total heat output;
high cost of manufacture; inconvenience and messiness in use; lack of
reliability, etc.
The present invention improves over prior-art heating devices by producing
heat with a unique, particulate or subdivided, electrochemical cell in
which there is an electrical short circuit across the anode and cathode of
the cell. Heating devices based on electrically shorted electrochemical
cells are not new per se, having been suggested, for example, in Kober,
U.S. Pat. No. 3,774,589 (heating blanket) and in McCartney, U.S. Pat. No.
3,884,216 (series of stacked plates, as in a vehicle battery). These
prior-art devices were based on a recognition that the heat-producing
electrochemical cell reactions are accelerated by the shorting paths,
which provide a highly efficient transfer of electrons between the cathode
and anode.
But the prior-art shorted electrochemical cells do not answer several
important needs in flameless heating devices. For example, Kober teaches a
"sandwich" or layered-type of heating blanket that comprises a metal foil
anode layer; an activated carbon cathode layer; a cotton batting separator
layer disposed between the anode and cathode and impregnated with salt;
and shorting members, such as staples or rivets, extending between the
anode and the cathode. This device is deficient in several respects that
limit its utility, e.g. in shelf-stability, because the shorting members
are susceptible to corrosion; in conformability, because of the stiffness
of the metal foil, which leads to imperfect heat transfer; in cost,
because of costly components and assembly methods; and in heat output,
because the layered nature of the structure limits the amount of heat that
can be generated from a heating blanket of given surface area. Similar
deficiencies are found in the rigid stacked-plate device taught in
McCartney; for example, such a device would never be adapted to
conformable wrapping around articles to be heated, which is a major desire
for flameless heating devices.
SUMMARY OF THE INVENTION
A heating device of the present invention includes an electrochemical cell
in which the anode comprises subdivided metal pieces and the cathode
comprises coatings on the metal pieces. The heating device may be
assembled with the cathode layers already coated on the subdivided anode
metal, or the cathode layers can be plated onto the anode metal in situ
after activation of the heating device by inclusion of a plating salt in
the electrolyte of the cell. The latter embodiment of the invention, which
is preferred, especially because of its lower manufacturing cost, may be
briefly summarized as generally comprising a container such as a flexible
envelope in which are disposed 100 mole-parts of a mass of subdivided
pieces of metal adapted to serve as the anode in an electrochemical cell;
a water-soluble electrolyte salt present in an amount sufficient to
provide a solution having a conductivity of at least 0.05 mho/centimeter
when dissolved in 500 mole-parts of water; and at least 0.25 mole-part of
a plating salt that provides metal ions adapted to react with the metal
anode pieces in the conductive solution, whereupon the metal from the
plating salt becomes plated onto the metal anode pieces to form the
cathode of an electrochemical cell.
Such a preferred heating device of the invention is activated by mixing
ingredients so as to envelop the metal anode pieces in the described
conductive solution of electrolyte and plating salts. Typically, the
activation is achieved by adding water, which is preferably either plain
water or water in which the electrolyte salt, plating salt, or both, are
dissolved. As an alternative, activation can be achieved by adding salts
to water in which the metal anode pieces have previously been disposed;
and the water added need not be pure, though many dissolved ingredients
other than the electrolyte and plating salts may impede reaction.
Upon activation, heat is produced at a controlled rate. Although some heat
will be produced simply by the direct reaction of the plating salt and the
metal anode pieces, by far the largest proportion of the heat produced
occurs through electrochemical reactions, including reduction of water to
hydroxyl ions and hydrogen gas at the cathode and oxidation of anode metal
at the anode. In general, at least 60 percent of the heat obtainable from
the heating device (as calculated from thermodynamic equations), and
preferably at least 90 percent, is produced through electrochemical
reactions. The reactions are controlled by the conductivity of the
solution and the availability at the anode and cathode of electrons or
ions necessary for the reaction; the latter availability can in turn be
controlled by the extent of the plating of the cathode on the metal anode.
As a result of this control, heating devices of the invention are capable
of producing a large and useful amount of heat very quickly and of
maintaining that heat for a lengthy period of time such as an hour or more
.
DESCRIPTION OF THE DRAWINGS
FIG. 1 is a sectional view through an illustrative heating blanket of the
invention;
FIGS. 2 and 3 are end views and sectional views, respectively, of the
heating blanket shown in FIG. 1;
FIG. 4 is a cross-sectional view through a different illustrative heating
blanket of the invention; and
FIG. 5 is a plot of heat output and electrical conductivity of heating
devices of the invention which include different amounts of the
electrolyte salt.
DETAILED DESCRIPTION
The illustrative heating blanket of the invention 10 illustrated in FIGS.
1-3 comprises a flexible envelope 11, subdivided or particulate
ingredients 12 within the envelope, and a layer 13 of thermal insulation
such as polymeric foam adhered to one side of the envelope by a layer 14
of adhesive. In use, the uncovered side 15 of the envelope 11 is placed
against or wrapped around an article to be heated; and the layer 13 of
insulation directs heat developed within the envelope to the article being
heated, as well as protects persons handling the envelope.
The envelope 11 is most conveniently made from synthetic polymeric films
such as polyethylene terephthalate; polyethylene; composite films of such
polymers, as described in Charbonneau et al, U.S. Pat. Nos. 3,188,265 and
3,188,266; or polyvinyl chloride. The films may carry a metal film to
reduce moisture penetration during storage. Such a metal film, which is
typically applied by vapor-deposition, may be covered by a protective
film. The polymeric films are typically sealed, welded, or adhesively
bonded around their edges to form a sealed or impermeable structure. In
the blanket shown in FIG. 1, the envelope 11 is shaped to provide a
filling spout 16, and at least the sealed portions at the top of the spout
are adapted to be separated to provide an opening through which the
blanket can be activated, as by addition of water or electrolyte. The
opening also serves as a vent allowing gaseous by-products of reactions in
the blanket to escape.
The invention may take the form of other heating devices besides flexible
blankets. For example, rigid containers can be used, so long as the
container is adapted to be placed against an article and to transfer heat
developed within the container to the article. Typically, the containers
are shallow and rather extensive in surface area.
The ingredients within the blanket 10 shown in FIGS. 1-3 include, as
previously noted, a subdivided metal adapted to serve as the anode in an
electrochemical cell. Such metals have a high electromotive force (greater
than +1) and exhibit a low rate of direct reaction with plain water (on
the order of the rate of reaction of magnesium with water, or slower).
Useful metals include magnesium (preferred), aluminum (somewhat less
preferred), titanium, and zirconium. To permit the best control of the
reaction, the anode pieces should have at least one dimension greater than
about 1 millimeter, though smaller pieces or powder can be used if a fast
reaction is desired. Thin metal chips are preferred, such chips generally
being less than a millimeter in thickness and less than 10 square
centimeters on a side; preferably they are less than about 1 square
centimeter on a side. Thin narrow ribbons, generally no more than a
centimeter in width, can be used, as can wires or wire-segments.
Sufficient metal is used to provide the desired total heat output, and all
together comprises a free-flowing or flexible mass.
The cathode layer on the metal anode pieces comprises a metal that has a
low electromotive force (less than +0.5). Particularly useful cathode
metals are copper, tungsten, iron, and nickel. A convenient method for
plating cathode metal onto the anode metal prior to assembly of the
heating device is to sputter-coat, vapor-deposit, or chemically deposit a
metal onto either the subdivided metal anode pieces, or onto a continuous
sheet of the anode metal which is later cut into chips.
Especially useful metals for in situ plating on the anode metal pieces are
copper, iron, or nickel, and convenient salts of such metals to use as the
plating salt are the sulfates, chlorides, and nitrates. The salt of the
plating metal should be in a particulate form and may be in very finely
divided form in order to assist its dissolving.
Also included in a heating blanket as shown in FIGS. 1-3 is a salt which
will dissolve in water to make a conductive electrolyte. Useful
electrolyte salts for this purpose include sodium chloride, calcium
chloride, and sodium nitrate. In general, these materials dissociate in
water to form high concentrations of mobile ions. Most often, the salt is
included in dry powder form in the heating blanket, though it can be
introduced in solution form at the time of activating the blanket; or be
added to water already present in the blanket.
As shown in FIG. 4, a heating blanket of the invention 20 can be completely
self-contained. In such a heating blanket, the envelope 21 has two
pouches, one pouch, 22, containing at least the metal anode pieces, and
the other pouch, 23, containing at least the electrolyte or water from
which the electrolyte is formed. The blanket 20 is activated by breaking
the seal 24 between the pouches. Envelopes as shown in FIG. 4, in which
two pouches are separated by a rupturable or separable seal, are quite
common and their method of manufacture is known in the art.
The proportions of the various ingredients can be varied to obtain
different results, e.g. different rates of reaction, different amounts of
heat, etc. Where metal anode pieces are used that have been preplated with
a cathode layer, the cathode layer generally covers at least 15 percent,
but less than 85 percent, of the surface of the anode pieces; plating of
50 percent of the surface is conveniently achieved by plating one side of
a sheet that is later cut up, and such a percentage of plating provides a
rate of heating useful for many kinds of jobs for heating devices of the
invention. Where the plating salt is used to provide in situ coating of
the anode pieces, it is generally used in an amount of at least 0.25
mole-part, and preferably at least 0.5 mole-part, per 100 mole-parts of
the metal anode pieces. On the other hand, the amount of plating salt
should be within a range such that at least 60 percent of the heat
obtainable by complete reaction of the ingredients will be produced by
electrochemical cell reactions. The plating salt will generally amount to
less than 50 mole-parts, and preferably less than 5 mole-parts, per 100
mole-parts of anode pieces. Where steady long-term heating is desired,
there is generally no advantage in use of more than 10 mole-parts of
plating salt per 100 mole-parts of anode pieces.
The electrolyte salt in a heating blanket of the invention can also be
varied to obtain different results. Such a variation in results is
indicated in FIG. 5, which provides two plots: first, a plot of the total
amount of heat produced during the first 10 minutes after activation of a
set of heating blankets of the invention as described in Example 5, each
containing a different amount of sodium chloride in the electrolyte (solid
points); and secondly, a plot of the conductivity of the solution at the
different amounts of sodium chloride (hollow points). The values plotted
are per gram of magnesium anode pieces and are for use of 3 milliliters of
water per gram of the magnesium. As may be seen, the greater the amount of
sodium chloride in the solution, the greater the conductivity, and the
greater the output of heat. At a conductivity represented by point A on
the curve, which corresponds to the conductivity of sea water, there is
very little output of heat. This conductivity does not provide
sufficiently rapid reduction of water to hydroxyl ions and hydrogen gas at
the cathode and oxidation of metal at the anode. However, when the
conductivity reaches a level of 0.05 mho/centimeter, then the
electrochemical reactions begin to occur with sufficient rapidity to
produce a desired rate of heating, and highest heat output is generally
obtained with conductivities of 0.1 mho/centimeter or more.
Heating blankets of the invention preferably include porous components that
control diffusion of the reactants within the heating blanket. For
example, the illustrative heating blanket shown in FIGS. 1-3 preferably
includes porous particulate fillers such as vermiculite, which is believed
to control and assure distribution of water in the heating blanket (i.e.
the passage of water is not choked off at folds of the envelope, since the
porous structure is present between the opposite sheets of the envelope).
Particles of manganese dioxide (such as the commercially available
"Manganor," supplied by Combustion Engineering) have also been found a
useful component to increase the heating rate at low temperatures. It is
desired to include such particles in a weight amount equal to at least 10
percent by weight of the metal anode pieces and preferably in an amount
equal to at least 20 percent of the weight of the metal anode pieces. Such
porous fillers preferably account for at least about 10 weight-percent,
and usually less than about 30 weight-percent of the particulate
ingredients within a heating blanket as shown in FIGS. 1-3. The heating
blanket shown in FIG. 4 uses a fibrous fabric, namely an inner sack 25 of
a fabric such as cotton, instead of particulate porous materials to
achieve desired diffusion of ingredients.
The invention will be further illustrated by the following example.
EXAMPLE 1
A heating blanket of the invention was prepared by placing a mixture that
included 40 grams of magnesium chips that averaged about 0.25 millimeter
in thickness and had average surface dimensions of about 4 millimeters by
6 millimeters and 15 grams of sodium chloride salt into a flat
5-inch-by-8-inch (12.5 centimeters by 20 centimeters) cotton pouch, and
then placing the cotton pouch inside a plastic envelope. The magnesium
chips carried a 5-micrometer-thick coating of copper covering about 50
percent of the area of each magnesium chip (i.e. the coating covered all
of one side of a flat chip). The blanket was wrapped around the side of a
sealed, water-filled polyethylene bottle and taped in place, after which a
1/4-inch-thick (0.6 centimeter) layer of foam insulation was adhered over
the exposed side of the blanket. The blanket was activated by adding 150
milliliters of water to the envelope, and the heat output produced in the
blanket and delivered to the water in the bottle was monitored with a
thermocouple immersed in the water. Heat delivered can be calculated from
the measurement of temperature by using the specific heat of water.
As a comparison, another heating blanket like that just described, except
that the magnesium chips were not coated with copper, but were left
uncoated, was prepared and measured for heat output. The heating blanket
of the invention delivered 40 times more heat in 1 hour than the
comparative heating blanket.
EXAMPLE 2
A heating blanket as described in Example 1 was prepared except that the
magnesium chips were coated with tungsten over about 50 percent of their
area instead of with copper. The heat delivered to the load was similar to
that delivered by the copper-coated chips as shown in the following table:
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Heat delivered to load
Example 1 Example 2
Time (calories/gram (calories/gram
(minutes) of magnesium) of magnesium)
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7 350 350
20 700 650
60 800 675
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EXAMPLE 3
A heating blanket was prepared and tested in the manner described in
Example 1, except that the magnesium chips were uncoated and the water
added to the heating blanket included 8 grams of CuCl.sub.2.2H.sub.2 O.
The latter served as a plating salt, with copper ions from the salt
producing an electroless deposition on the magnesium chips; and the
deposited layer then served as a cathode for acceleration of the
electrochemical reaction. The electroless deposition was itself
exothermic, but thermodynamic calculations show that the energy
contributed by that exothermic reaction was no more than 6 percent of the
energy available from the complete electrochemical oxidation of magnesium
by water. The following heating rate was observed:
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Time Heat delivered to load
(minutes) (calories/gram of magnesium)
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7 300
20 675
60 900
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EXAMPLE 4
A heating blanket was prepared that included, per square inch (6.5 square
centimeters) of the surface area of the blanket, 1 gram of magnesium chips
that averaged 4 millimeters by 6 millimeters by 0.25 millimeter in size,
0.4 gram of ferric sulfate, 1.25 gram of sodium chloride, 0.3 gram of
vermiculite, and 0.3 gram of manganese dioxide ("Manganor" supplied by
Combustion Engineering). One-hundred-fifty milliliters of water were added
to the heating blanket to activate the heating blanket, and heat was
generated and delivered to the load in an amount of 525 calories/gram of
magnesium over a period of 20 minutes.
EXAMPLE 5
To illustrate the variation that occurs in heat output depending on the
amount of plating salt present in the blanket, a set of heating blankets
were prepared of the type generally described in Example 4 except that the
blankets had an area of 12 square inches (78 square centimeters) instead
of 40 square inches (260 square centimeters), and the amount of
ingredients was correspondingly reduced (so there was still one gram of
magnesium per 6.5 square centimeters of surface area). The amount of
ferric sulfate in the blankets varied from zero to 0.7 gram per gram of
magnesium chips. To minimize heat losses to the ambient environment and
thus cause more heat to be delivered to the load, each blanket was
attached to two polyethylene bags filled with a total of 200 grams of
water, with the temperature of the water being monitored with a
thermocouple, and the bags then placed in a polystyrene container. The
results are shown in the following table:
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Heat delivered to load
Parts of ferric sulfate
after 10 minutes
(grams) (calories/gram of magnesium)
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0 50
0.05 750
0.1 1500
0.2 1250
0.3 1525
0.4 1575
0.5 1775
0.67 1700
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(When "Manganor" was omitted as well as ferric sulfate from a heating
blanket as described in Example 4, the heat delivered to the load after 10
minutes was only 5 calories per gram of magnesium).
EXAMPLE 6
Two heating blankets were prepared and tested as described in Example 5
except that no vermiculite and no "Manganor" were included in the
formulation and in one of the blankets the magnesium chips were replaced
with an equal weight amount of magnesium powder (100 percent passed a 40
mesh, U.S. Standard screen). The average heating rate obtained from the
two blankets is given in the following table to illustrate that
larger-sized anode metal pieces provide a longer heating cycle.
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Average heating rate during
different time intervals
Time interval
(calories/gram of magnesium/minute)
(minutes) Magnesium powder
Magnesium chips
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0-5 332 227
5-10 5 82
10-20 6.5 33
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