FIELD OF THE INVENTION
[0001] This invention relates to an improved, eocnomical, efficient process for generating
an acetylene base fuel gas of enhanced stability and safety and of high BTU content
that will burn, for example, to heat boilers or power internal combustion engines,
with a minimum amount of deleterious emissions. The invention also relates to a process
for producing an acetylene base fuel gas with no undesirable by-products, such as
calcium hydroxide, which create disposal problems. Instead, the by-product of this
process is an excellent top cylinder lubricant (TCL) when the gas is used as a fuel
for internal combustion engines.
BACKGROUND OF THE INVENTION
[0002] The making of acetylene gas from the reaction of water with calcium carbide has long
been known. There are in fact two processes, one known as the "wet" process and the
other as the "dry", both being disclosed in the U.S. patent to Osborg, No. 2,785,052,
granted March 12, 1957. In both processes the industry has long been plagued with
the disposal of the unwanted residue, namely, calcium hydroxide or lime. In the wet
process, the residue is a wet slurry of hydrated lime. In the dry process, the residue
is in the form of a substantially dry powder, some of which becomes entrained with
the acetylene gas and desirably is filtered out before the gas is burned, as disclosed
in U.S. Patent to Foster No. 3,498,767. In any event, disposal of the unwanted residue
of lime is a considerable problem in the industry. Furthermore, both processes are
exothermic and develop considerable heat so that cooling means must be provided to
maintain the acetylene at a safe temperature.
[0003] Moreover, the acetylene produced by both processes is thermodynamically unstable
even at room temperatures and even in the absence of air, as is well known in the
art. The thermal decomposition of acetylene can proceed so rapidly that explosions
and detonations may result. Consequently, governmental safety regulations prescribe
detailed procedures for handling, storage, and shipment of acetylene.
[0004] An old Belgian Patent No. 132,113, dated November 26, 1897, suggests that acetylene
can be produced without an unwanted wet lime by-product by reacting an acid, e.g.,
hydrochloric acid, with calcium carbide to produce acetylene and calcium chloride.
The patent states that the main success of such reaction is the slow release of the
gas. That patent discloses that the acid is sprayed onto a bed of carbide. According
to applicant's experience, however, the reaction of calcium carbide with hydrochloric
acid is quite violent and extremely difficult to regulate, particularly when the carbide
is added to the liquid acid. Furthermore, and contrary to the teachings of the Belgian
patent, it has been found that the addition of acid to calcium carbide results in
a frothy and unworkable mass which inhibits the release of the gas. It also has been
suggested, e.g., U.S. Patent to Mackusick No. 588,230, August 17, 1897, that the reaction
of calcium carbide with water to produce acetylene can be slowed and made more uniform
by the addition of glycerine or other substances, e.g., dextrine, sugar, glucose,
etc. to the water. The above-mentioned Osborg patent also suggests the addition of
an inert "carrier" liquid, e.g., an alcohol, an amine, or a glycol, to the water to
have better control and reduce the exothermic heat of the reaction. The addition of
a glycol to the water for anti-freeze purposes also is suggested in "Acetylene, Its
Properties, Manufacture and Uses" by Miller, VoL I, 1965, Academic Press, pages 291-192.
Unfortunately, each of the processes of Mackusick, Osborg and the publication "Acetylene,
etc." remain plagued by the formation of unwanted lime as a by-product.
[0005] With the advent of shortages of common liquid fuels for internal combustion engines
such as gasoline, diesel fuel and the like, increased attention has been directed
recently toward operation of internal combustion engines on gaseous fuels which are
not in such short supply and/or which may be produced by refining techniques which
are less complicated and expensive than those employed in the production of conventional
liquid fuels. For example, much effort has been directed recently to the use of normally
gaseous fuels, such as propane, hydrogen, natural gas, ammonia, and the like. Prior
workers, however, have concluded that acetylene, which can be produced by relatively
simple technology in low-pressure generators by reacting calcium carbide with water,
cannot be employed practically to power internal combustion engines because of the
particulate reaction product, i.e., calcium hydroxide, which, if not filtered out,
is carried into the engine from the generator and also because the high combustion
temperatures of acetylene create problems in obtaining adequate cylinder lubrication.
In fact, an internal combustion engine fueled by acetylene produced by conventional
processesd will soon "burn out".
[0006] Thus, despite the fact that acetylene is a very clean burning fuel, having a relatively
high thermal energy content, little attention has been directed to its use as an automotive
fuel or for use in firing steam boilers, etc.
[0007] Economic studies reveal that plentiful sources of raw materials, e.g., coal and limestone,
are currently available in the United States for the production of solid calcium carbide,
these sources being independent of the world petroleum supply. Further studies have
now indicated that improved methods are available for producing solid calcium carbide
readily and inexpensively from these sources. In the substantial quantities of the
raw materials which would be required for use in producing acetylene gas, for powering
internal combustion engines for automobiles and other vehicles (see, for example,
U.S. Patent No. 3,664,134), firing boilers, heating residences and office buildings,
etc., it appears that improved processes for producing calcium carbide, together with
the process for producing an improved fuel gas therefrom as disclosed herein, can
compete most effectively with other conventional processes for producing fuels from
conventional fuel materials such as petroleum, coal, oil shale, etc.
[0008] One disadvantage attendant the use of calcium carbide as a fuel source is its great
tendency to hydrolize readily in air. To overcome this problem calcium carbide presently
is stored and shipped in sealed drums, a considerable expense when large amounts are
involved. The U.S. Patent to Lancaster, No. 683,562, dated October 1, 1901, suggests
coating the carbide with various water impervious substances, such as mixtures of
petroleum, glucose and carbonate of lime, a mixture of paraffin wax, cocoa butter
and sugar. Before use, however, the coated carbide must be broken up to provide access
of water thereto. That patent also suggests saturating the carbide with creosote,
plain or diluted, to protect it from air or water. If the creosote is undiluted, however,
it must be neutralized with potassium hydrate or other suitable alkali before the
carbide is used to produce acetylene by contact with water. If the creosote is diluted,
the protection from air or water is weakened greatly, although the carbide may be
used without neutralization but with the acetylene- generating reaction with water
slowed considerably. These prior processes for avoiding premature hydrolysis of carbide
suffer from the problem that pretreatment of the carbide prior generation of acetylene
is required or else the generation slowed to an impractical rate.
[0009] Accordingly, it is an object of this invention to provide an improved, economical,
efficient process for the production of an acetylene base, more stable, safer fuel
gas of high BTU content by the reaction of calcium carbide with an inexpensive liquid
reagent, which gas can be directly utilized as an efficient gaseous fuel for internal
combustion engines and in other applications, such as production of electricity, etc.,
with a minimum of deleterious emissions.
[0010] It is another object of this invention to provide such a process which does not produce
an undesirable by-product residue which could create problems of waste disposal and
use of the gas in internal combustion engines.
[0011] It is another object of this invention to provide such a process which will produce
an acetylene base fuel gas which contains by-product compounds that form an advantageous
top cylinder lubricant for an internal combustion engine.
[0012] A further object of the present invention is to provide a novel top cylinder lubricant
composition which forms a part of an acetylene base fuel gas for an internal combustion
engine.
[0013] These and other objects of the present invention will become more apparent from the
following detailed description.
SUMMARY OF THE INVENTION
[0014] In accordance with the present invention, there is provided an improved process for
producing an acetylene base relatively safe fuel gas of enhanced stability which comprises
reacting a metal carbide (preferably an alkylene earth metal carbide) with an aqueous
liquid activator reagent comprising water, a water-soluble reaction-rate-controlling
substance (preferably a lower alkylene glycol) and a strong inorganic acid, such as
hydrochloric, sulfuric, phosphoric, carbonic or nitric or mixtures thereof. Attendant
to this process is the production of an acetylene base fuel gas which contains a top
cylinder lubricant composition. In the preferred embodiment of the present invention,
calcium carbide is reacted with a liquid aqueous activator reagent which comprises
water, a lower alkylene glycol (preferably ethylene glycol) and a strong inorganic
acid (preferably hydrochloric acid).
[0015] In order to provide a more stable reactant which has a longer storage life, the invention
further provides a means for stablizing calcium carbide so as to render it impermeable
to air and moisture by coating particles of calcium carbide with an air and moisture
impermeable film, preferably of nitrocellulose and a polyester resin, which is attacked
and dissolved when brought in contact with the aqueous liquid activator reagent of
the present invention.
[0016] The acetylene base fuel produced according to the present invention is a gaseous
reaction product which further includes vaporized or entrained by-product compounds
which are a most effective top cylinder lubricant for an internal combustion engine.
[0017] The advantages attendant to the processes and fuel of the present invention are many.
Thus utilizing the activator reagent of the present invention, one obtains an unexpected
amount of acetylene base fuel produced over what has been obtained in the art heretofore.
Thus utilizing the reaction of the present invention, one is able to obtain up to
8 cubic feet of fuel gas for each pound of calcium carbide reacted which contrasts
to the approximately 4.5 cubic feet of actylene obtained by conventional water and
carbide reaction processess. Furthermore, the acetylene base fuel gas produced according
to the present invention exhibits enhanced BTU output over that of natural gas, i.e.,
up to about 1447 per cubic foot for the gas of the present invention as contrasted
to about 1448 BTU for pure acetylene and about 879 BTU for natural gas.
[0018] A significant advantage which resides in the process herein disclosed is the elimination
of lime waste disposal problems attendant the conventional reaction of calcium carbide
with water. Utilizing the aqueous liquid activator of the present invention the formation
of lime waste by-product is eliminated and provides for a reagent medium which can
be used for extended periods of time without replenishment.
[0019] Furthermore, the acetylene base fuel gas which is produced in accordance with the
present invention is characterized by having enhanced storage capabilities. Previously,
acetylene produced according to conventional methods from carbide needs be made in
a reactor and stored in the presence of a flammable solvent filler, such as acetone,
at a pressure not to exceed 15 psi. The acetylene base fuel gas obtained according
to the present invention may be stored at relatively high pressures (e.g., up to 250
psi) without the presence of a solvent filler such as acetone, thereby permitting
high storage capabilities. Storage in the presence of the activator actually enhances
the ability of the gas to be stored at high pressures. Furthermore, the acetylene
base fuel gas obtained in accordance with the present invention is relatively stable
and will not decompose readily at room temperatures, even in the presence of air.
As a result, in generating the acetylene base fuel gas according to the present invention
one need not purge the reaction vessel of air prior to reaction.
[0020] A further advantage of the process of this invention is that the reaction is far
less exothermic than that of calcium carbide with water alone. In fact, the amount
of heat generated in the reaction is so low as to require no cooling of the generator.
The reaction of calcium carbide in water results in a heat of reaction of 215° F whereas
the heat of reaction utilizing the reagent of the present invention is 140° F.
DETAILED DESCRIPTION OF THE INVENTION
[0021] The present invention provides a process for producing an acetylene base fuel gas
which comprises the steps of reacting carbide, preferably an alkaline earth metal
carbide, with an aqueous liquid activator reagent composed of water, a water-soluble
reaction-rate-controlling substance (preferably a water-soluble lower alkylene glycol)
and an inorganic strong acid.
[0022] The preferred carbide is calcium carbide. It will be appreciated by those skilled
in the art, however, that other carbides can be employed, such as aluminum carbide
and iron carbide, at a resulting increase in cost.
[0023] Suitable inorganic strong acids include hydrochloric, sulfuric, phosphoric, carbonic
and nitric acids, or mixtures thereof, with hydrochloric acid being preferred for
ready availability, low cost and lack of unpleasant side reactions.
[0024] The reaction-rate-controlling substance not only retards the rate of reaction but
also contributes to the stability of the gas produced. In addition the substance serves
to lower the reaction temperature. Suitable reaction-rate-controlling substances are
water-soluble alkylene glycols and water-soluble alcohols, or mixtures thereof, with
the glycols being preferred because of their inflammability.
[0025] Preferably, the liquid activator reagent is prepared by mixing the water and substance
components and then introducing the acid, such as hydrochloric acid, into the water-substance
mixture. The carbide then is added, at a controlled rate, to the reagent, rather than
vice-versa, for better control of the release of gas.
[0026] The reaction of the liquid activator reagent with calcium carbide can be carried
out at atmospheric pressure or at moderate pressures, say on the order of 18 psi,
and produces a fuel gas containing upwards of 89%, or even more, acetylene, which
fuel gas also contains vaporized and/or entrained compounds which form a most effective
top cylinder lubricant for an internal combustion engine.
[0027] Acceptable ranges of weight proportions of the components of the liquid activator
reagent are about

[0028] A decrease in the proportion of the glycol in the reagent increases the reaction
rate and vice-versa. Similarly, an increase in the proportion of the acid increases
the reaction rate and vice-versa. In the preferred proportion ranges of the reagent,
the reaction proceeds uniformly and relatively slowly without foaming (which occurs
in the conventional "wet" method of producing acetylene and which inhibits release
of the gas) and without the formation of a by-product hydroxide percipitate. If the
glycol proportion is decreased below the minimum level, the gas tends to become unstable
and hazardous like acetylene generated by the reaction of calcium carbide with water
only. Consequently, the glycol proportion should be large enough to insure stability
of the gas with the attendant advantage of being subjectable to higher pressures without
danger, and so that the reaction can be better controlled, i.e., uniformly regulated.
Further, a decrease in the glycol proportion results in a decrease in the TCL by-product,
so it would seem that the glycol enters into the reaction. If the acid proportion
is decreased below the minimum level, an undesirable hydroxide by-product precipitate
is formed which presents a disposal problem.
[0029] In the preferred ranges, however, and in even the acceptable ranges, the gas is produced
at a uniform rate leaving a greasy oily by-product residue, having some particulate
matter, floating on the liquid reagent. This residue can be removed easily by circulating
the reagent through an appropriate filtering system. When heated and filtered, the
by-product residue forms an excellent lubricant for moving parts. The reagent can
be used for long periods of time without replenishment. Thus, the main reactant is
the carbide.
[0030] Some of the by-product residue is entrained and/or vaporized with the gas and will
burn therewith. When the gas is used as a fuel for an internal combustion engine,
the by-product residue mixed therewith forms an excellent top cylinder lubricant (TCL)
which is drawn into each cylinder on the fuel intake stroke of the piston and burned
with the gas on the power stroke. Thus, the TCL is constantly replenished in the cylinder.
The efficacy of the by-product residue as TCL has been demonstrated by use of the
gas as fuel for a Tecumseh air-cooled, one cylinder, 3 HP internal combustion engine.
The engine has been so fueled and operated for at least 1000 hours, sometimes at over
rated RPMs, with no signs of cylinder, piston, piston ring, or valve wear. Examination
of the cylinder shows no build-up or hardening of the TCL by-product and that its
lubricating qualities are most efficacious under the cylinder's high temperature operating
conditions. The gaseous fuel also has been used to power several automobile engines
with similar beneficial lubricating results. This is in marked contrast to an engine
which when fueled by substantially pure acetylene will "burn out" after a few hours
of operation without addition of lubricant to the cylinder.
[0031] Moreover, the gaseous fuel of this invention mixes with air more readily than gasoline
and when burned produces far less undesirable and deleterious emissions than the burning
of gasoline and air. In fact, a 1974 Dodge van with no catalytic converter was equipped
to be selectively powered with gasoline or the gaseous fuel of this invention and
the emissions were measured by a State of Arizona vehicle inspection station. The
maximum emissions allowed at that inspection were 400 parts per million (PPM) of hydrocarbon
(HC) and 5.5% carbon monoxide (CO). When powered with gasoline the inspection emission
results were 410 HC (PPM) and 14.5% CO and the vehicle failed to pass inspection.
When powered with the gaseous fuel of this invention, however, the inspection emission
results were 60 HC (PPM) and 0.14% CO and the vehicle passed the inspection by a large
margin.
[0032] More recent comparative tests with a 1974 Chevrolet 350 V-8 engine not equipped with
a post combustion emission control device, e.g., a catalytic converter, when idling
at 850 RPM produced emissions when selectively powered with three types of fuels as
follows:

Preparation of Liquid Activator Reagent
[0033] As distinguished from prior art production of acetylene by hydrolysis of calcium
carbide, the process of the present invention employs a special 3-component liquid
activator reagent which reacts with the calcium carbide to achieve the results described.
The liquid activator reagent comprises water, a water-soluble alkylene glycol or alcohol
and a strong inorganic acid, preferably hydrochloric acid.
[0034] The term "water-soluble alkylene glycol", as used herein, is intended to include
all glycols having substantial solubility in water. For example, in the practice of
my invention, one can employ ethylene glycol, propylene glycol, 1,3-propanediol, meso-2,3-butanediol,
1,4-butanediol, glycerol (1,2,3-propanetriol), cis-1,3-cyclopentanediol and 2-methyl-l,2-pentanediol.
[0035] Preferably, from the standpoint of each of handling, cost and availability, ethylene
glycol is employed in the formation of the liquid activator reagent.
[0036] The term "water-soluble alcohols", as used herein, is intended to include all alcohols
(primary, secondary and tertiary) having substantial solubility in water and generally
includes those having from 1 to 8 carbon atoms. Suitable alcohols include methanol,
ethanol, isopropanol, butanol and mixtures thereof. Alcohols are not preferred, however,
because in general they make the activator reagent flammable.
[0037] According to the presently preferred practice of the present invention, the glycol
component is merely mixed with the water component of the activator, for example,
in a vessel containing an appropriate agitator, and the acid is then added to the
water-glycol mixture. The relative proportions of water, glycol and acid in the liquid
activator reagent will have an effect on the rate of the reaction, the final composition
of the fuel gas, and the by-product residue or top cylinder lubricant which are produced
when the liquid activator reagent is reacted with calcium carbide.
[0038] The water present in the aqueous liquid activator reagent may be added separately
or obtained from the acid employed. The amount of water present must be sufficient
to provide the necessary reaction with the carbide material. The presence of the alkylene
glycol serves to control the rate of reaction and hence rate of formation of the acetylene
base fuel gas, as well as the amount of the TCL by-product, and should be sufficient
to provide a smooth even generation of safer more stable gas and an adequate amount
of TCL when the gas is used to fuel an internal combustion engine.
[0039] The presence of the strong inorganic acid should be sufficient to eliminate the formation
of a lime (calcium hydroxide) by-product.
[0040] In commercial usage, the liquid reagent of this invention can be prepared and shipped
as a two-component concentrate composition, namely, a mixture of a water-soluble alkylene
glycol or alcohol and a strong inorganic acid in proper proportions, the mixture to
be added to the appropriate amount of water at the reaction site. This procedure avoids
the cost of shipping the water component of the reagent. A suitable concentrate contains
from about 35 to 82% by weight of the glycol or alcohol component, e.g., ethylene
glycol, and from about 18 to 65% by weight of the acid. Such a concentrate when mixed
with water forming about 30 to 60% by weight of the mixture results in the desired
activator reagent.
[0041] In order to enhance the capability of calciuim carbide used in the reaction of the
present invention to be stored without deterioration, it is preferred to stabilize
the calcium carbide particles so as to render the same impermeable to air and moisture.
This is accomplished by coating the particles of calcium carbide with a film, impervious
to air and moisture but dissoluble by the reagent, preferably composed of nitrocellulose
and a polyester resin. In carrying out such a process, one merely contacts the particles
of calcium carbide with a slurry of nitrocellulose and polyester resin in a suitable
organic solvent such as acetone, isopropyl alcohol or mixtures thereof. After contacting
the calcium carbide particles with the slurry, the excess slurry is drained and the
particles may be dried, for example in a convection dryer, to yield particles having
a film thereon impermeable to air and moisture. While the resulting coated particles
are impermeable to air and moisture, upon contact with the aqueous liquid activator
reagent of the present invention, the coating is broken down or dissolved and reaction
occurs to generate the desired acetylene base fuel gas.
[0042] An example of a suitable slurry for coating the carbide granules is:

Fuel Gas and TCL Formation
[0043] The fuel gas and associated by-product residue which is an excellent top cylinder
lubricant (TCL), are formed by reacting the liquid activator reagent, described above,
with granular calcium carbide. The calcium carbide is metered, as required, into a
closed reactor or generator containing the liquid activator reagent to produce the
requisite quantity of the gaseous acetylene base fuel. The generator desirably is
operated at approximately 15-20 psi, preferably aboaut 1.8 psi. The reaction goes
to completion when the quantity of water in the liquid activator reagent in the generator
is approximately stoichiometrically equivalent to the calcium carbide metered and
charged to the generator, according to the theoretical equation

Any calcium hydroxide produced by the reaction is converted to a soluble salt, e.g.,
CaCl, by reaction with the acid and goes into solution in the reagent. Experiments
have shown that the reagent is not consumed appreciably during prolonged practice
of the process and needs to be replaced or replenished only after prolonged use. It
is desirable, however, to periodically or continuously filter out the by-product floating
residue.
Production of TCL
[0044] The mechanism of the formation of and the exact identity of TCL in the gaseous acetylene
base fuel is not yet fully understood, but it would appear that the ethylene glycol
enters into the reaction. All that is presently known is that at least a portion of
the calcium moiety of the solid calcium carbide fuel appears to react with the glycol
and acid components of the liquid activator reagent to form a compound which is at
least transiently volatile, or is entrained, and some of which passes from the generator
along with the gaseous fuel. The mixture of the compound and gaseous fuel then can
be fed into the carburetor of an internal combustion engine or to a fuel burner for
a boiler or the like. Experimental observation has determined that the TCL compound
is present in a substantially constant amount in the upper portion of the combustion
cylinders of an engine when fueled by the gas of this invention.
[0045] As indicated, the step of production of the liquid activator reagent consists of
two sub-steps involving the mixing of water and the alkylene glycol component. The
mixed water-glycol composition is then further mixed by addition of the acid thereto
followed by additional mixing. In the event the acid and alkylene glycol components
are mixed first and this reagent concentrate shipped for a reduction in shipping costs,
this concentrate is added to the appropriate amount of water at the reaction site.
The resulting liquid activator reagent is then charged into a gas production generator
into which solid calcium carbide granules are metered. The reaction product from the
generator, comprising the acetylene base gas-TCL composition mixture is then metered
to its point of use, i.e., a burner for a boiler or the like or the carburetion system
of an internal combustion engine, where it is burned to provide power.
[0046] It has been found that with a liquid reagent having proportions within the preferred
ranges, about 8 cu. ft. of gaseous fuel is produced from each pound of calcium carbide,
with the gaseous fuel having a molecular weight of about 26.3, specific gravity of
.908 and BTU content of up to at least 1447 per cubic foot (dry basis) at 14.695 psia
and 62°F. This compares most favorably with the production of acetylene gas from the
reaction of calcium carbide with water alone of only about 4.5 cubic feet of gas per
pound of carbide with the acetylene having a BTU content of about 1448 per cubic foot.
[0047] The following examples are offered to more fully illustrate the invention but are
not to be construed as limiting the scope thereof:
EXAMPLE ONE
[0048] Into an eight gallon pressure steel reactor was placed 4 gallons of activator having
the following composition:

Thereafter, one pound of calcium carbide granules (0.25 inch mesh) was metered in
quarter pound increments into the activator solution at a rate so as to maintain the
reactor pressure at 15 psia. After purging, a sample of the gas produced was collected,
analyzed and found to have the following composition:

[0049] The gaseous product had a molecular weight of 26.3, specific gravity of 0.909 (calculated)
and a heating value (BTU-calculated) of 1358 per cubic foot (dry basis) at 14.696
psia at 60" F.
[0050] The presence of the sulfide undoubtedly was due to impurities in the calcium carbide.
EXAMPLE TWO
[0051] The procedure of Example One was repeated using an activator having the following
composition (parts by weight):

The resulting gas was collected in a collection tube at 16 psia and upon analysis,
found to have the following composition:

The gaseous product had a specific gravity of 0.894 (calculated) and a heating value
(BTU-calculated) of 1424 per cubic foot (dry basis) at 14.696 psia at 60°F.
EXAMPLE THREE
[0052] In the same manner as Example One, fuel gas was generated by reacting calcium carbide
with an activator having the following composition (parts by weight):

The resulting gas was collected in a collection tube at 25 psia and upon analysis
found to have the following composition:

[0053] The gaseous product had a specific gravity of 0.892 (calculated) and a heating value
(BTU-calculated) of 1437 per cubic foot (dry basis) at 14.696 psia at 60°F.
[0054] The gas produced as described can fuel the internal combustion engine of an automobile
without detectable atmospheric pollution, with about one-half the amount of acetylene
base gas being required to power the engine as compared to natural gas.
[0055] It thus will be seen that the objects and advantages of this invention have been
fully and effectively achieved. It will be realized, however, that the foregoing specific
embodiments have been disclosed only for the purpose of illustrating the principles
of this invention and are susceptible of modification without departing from such
principles. Accordingly, the invention includes all embodiments encompassed within
the spirit and scope of the following claims.
1. A process for the production of an acetylene base stable fuel gas which comprises
reacting metal carbide with an aqueous liquid activator reagent comprising water,
a water-soluble reaction-rate-controlling substance and an inorganic strong acid.
2. A process according to claim 1 wherein the carbide is an alkaline earth metal carbide.
3. A process according to claim 2 wherein the carbide is calcium carbide.
4. A process according to claim 1 wherein the substance is selected from the group
consisting of an alkylene glycol and an alcohol and mixtures thereof.
5. A process according to claim 4 wherein the alkylene glycol is selected from the
group consisting of ethylene glycol, propylene glycol, 1,3-propanediol, meso-2,3-butanediol,
1,4-butanediol, glycerol, cis-1,2-cyelopentanediol and 2-methyl-l,3-pentandiol.
6. A process according to claim 5 wherein the glycol -is ethylene glycol.
7. A process according to claim 1 wherein the inorganic strong acid is selected from
the group consisting of hydrochloric, sulfuric, phosphoric, carbonic, nitric and mixtures
thereof.
8. A process according to claim 7 wherein the inorganic strong acid is hydrochloric
acid.
9. A process according to claim 1, 2, 3, 4, 5, 6, 7 or 8 wherein the proportion of
acid in the reagent is sufficient to substantially prevent the formation of calcium
hydroxide by-product residue.
10. A process according to claim 1, 2, 3, 4, 5, 6 or 7 wherein the proportion of the
substance in the reagent is sufficient to substantially insure stability of the gas.
11. A process according to claim 1, 2, 3, 4, 5, 6 or 7 wherein the proportion of acid
in the reagent is sufficient to substantially prevent the formation of calcium hydroxide
by-product residue and the proportion of the substance in the reagent is sufficient
to substantially insure stability of the gas.
12. A process according to claim 1, 2, 3, 4, 5 or 7 wherein the fuel gas as produced
includes a by-product effective as a top cylinder lubricant for an internal combustion
engine.
13. A process according to claim 4 or 7 in which the liquid activator reagent is prepared
by mixing the water and substance components and introducing the acid into the water-substance
mixture.
14. A process according to claims 6 and 8 in which the weight proportions of the components
of the reagent are about
15. A process according to claims 6 and 8 in which the weight proportions of the components
of the reagent are about
16. A process according to claim 1, 2, 3, 4, 5 or 7 wherein the carbide which is employed
is characterized by the presence of an air and moisture impermeable coating which
is dissoluble by said reagent.
17. A process according to claim 16 wherein the coating is formed from nitrocellulose
and a polyester resin.
18. A process for stabilizing calcium carbide so as to render it impermeable to air
and moisture which comprises coating particles of calcium carbide with a film substantially
impervious to air and water but dissoluble by the reagent defined in claim 1, 4 or
7.
19. A process according to claim 18 wherein the film comprises nitrocellulose and
a polyester resin.
20. A process according to claim 19 which comprises the steps of:
(a) contacting particles of calcium carbide with a slurry of nitrocellulose and a
polyester resin in an orgnic solvent;
(b) removing excess slurry from the particles; and
(c) drying the particles to evaporate the solvent whereby the particles are impermeable
to air and moisture but are reactive with an aqueous liquid activator comprising water,
a water-soluble reaction-rate-controlling substance and a strong inorganic acid to
produce an acetylene base fuel gas.
21. An aqueous liquid activator reagent for use with metal carbide to generate an
acetylene base fuel gas which comprises water, a water-soluble reaction-rate-controlling
substance and a strong inorganic acid.
22. The reagent of claim 21 wherein the substance is selected from the group consisting
of an alkylene glycol and an alcohol and mixtures thereof.
23. The reagent of claim 22 wherein the substance is a glycol selected from the group
consisting of ethylene glycol, propylene glycol, 1,3-propanediol, meso-2,3-butanediol,
1,4-butanediol, glycerol, eis-1,2-cyclopentanediol, and 2-methyl-l,3-pentanediol.
24. The reagent of claim 23 wherein the glycol is ethylene glycol
25. The reagent of claim 21 wherein the acid is selected from the group consisting
of hydrochloric, sulfuric, phosphoric, carbonic and nitric.
26. The reagent of claim 25 wherein the acid is concentrated hydrochloric acid.
27. The reagent of claim 24 and 26 wherein the ranges of weight proportions of the
components of the reagent are about
28. A liquid activator reagent concentrate to be added to a predetermined amount of
water to form a reagent for reaction with a metal carbide to generate an acetylene
base fuel gas which comprises a water-soluble reaction-rate-controlling substance
and a strong inorganic acid.
29. A concentrate according to claim 28 wherein the substance is selected from the
group consisting of an alkylene glycol and an alcohol and mixtures thereof.
30. A concentrate according to claim 29 wherein the substance is a glycol selected
from the group consisting of ethylene glycol, propylene glycol, 1,3-propanediol, meso-2,-butanediol,
1,4-butanediol, glycerol, cis-l,2-cyelopentanediol and 2-methyl-l,3-pentanediol.
31. A concentrate according to claim 30 in which the glycol is ethylene.
32. A concentrate according to claim 28 wherein the acid is selected from the group
consisting of hydrochloric, sulfuric, phosphoric, carbonic and nitric.
33. A concentrate according to claim 32 wherein the acid is concentrated hydrochloric
acid.
34. A concentrate according to claim 31 and 33 wherein the ranges of weight proportions
of the components are about
35. A top cylinder lubricant composition comprising a reaction by-product produced
by reacting metal carbide with a liquid activator reagent comprising water, a water-soluble
reaction-rate-controlling substance and a strong inorganic acid.
36. A composition according to claim 35 in which the substance is selected from the
group consisting of a glycol and an alcohol and mixtures thereof.
37. A composition according to claim 36 in which the substance is ethylene glycol.
38. A composition according to claim 35 in which the acid is selected from the group
consisting of hydrochloric, sulfuric, phosphoric, carbonic and nitric and mixtures
thereof.
39. A composition according to claim 38 in which the acid is concentrated hydrochloric.
40. The gaseous reaction product of the reaction of claim 1, 2, 3,4, 5 or 7.
41. The gaseous reaction product of the reaction of claim 40 which includes a vaporized
or entrained by-product of the reaction which forms a top cylinder lubricant.
42. A lubricant composition according to claim 41 in which the weight percentages
of the components of the liquid activator reagent are about
43. A lubricant composition according to claim 41 in which the weight percentages
of the components of the liquid activator reagent are about
44. A method of operating an internal combustion engine comprising introducing as
the fuel component of the fuel-air charge for said engine, the acetylene base fuel
gas produced by the process of claim 1, 2, 3, 4, 5 or 7.
45. The reagent of claim 24 and 26 wherein the ranges of weight proportions of the
components of the reagent are about
46. A composition according to claims 36 and 38 in which the carbide is calcium.