US2684339A - Process of preparing a napalm composition containing a finely divided inert carrier - Google Patents

Process of preparing a napalm composition containing a finely divided inert carrier Download PDF

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Publication number
US2684339A
US2684339A US250560A US25056051A US2684339A US 2684339 A US2684339 A US 2684339A US 250560 A US250560 A US 250560A US 25056051 A US25056051 A US 25056051A US 2684339 A US2684339 A US 2684339A
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napalm
soap
inert carrier
organic acids
aluminum
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US250560A
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Albert O Herron
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Safety Fuel and Chemical Corp
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Safety Fuel and Chemical Corp
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    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10LFUELS NOT OTHERWISE PROVIDED FOR; NATURAL GAS; SYNTHETIC NATURAL GAS OBTAINED BY PROCESSES NOT COVERED BY SUBCLASSES C10G, C10K; LIQUEFIED PETROLEUM GAS; ADDING MATERIALS TO FUELS OR FIRES TO REDUCE SMOKE OR UNDESIRABLE DEPOSITS OR TO FACILITATE SOOT REMOVAL; FIRELIGHTERS
    • C10L7/00Fuels produced by solidifying fluid fuels
    • C10L7/02Fuels produced by solidifying fluid fuels liquid fuels
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C51/00Preparation of carboxylic acids or their salts, halides or anhydrides
    • C07C51/41Preparation of salts of carboxylic acids
    • C07C51/412Preparation of salts of carboxylic acids by conversion of the acids, their salts, esters or anhydrides with the same carboxylic acid part

Definitions

  • This invention relates to improved napalm.
  • the napalm produced according to this method is generally not uniform in appearance and usually consists of crumbly and tacky granular particles.
  • One object of this invention is the production of a uniform, finely pulverulent napalm without grinding.
  • a further object of this invention is a napalm which may be used to gel gasoline in a highly satisfactory manner at any temperature above freezing.
  • a still further object of this invention is a napalm which may be used to gel gasoline in an excellent manner without the addition of xylenol.
  • the inert carrier material should be finely divided and have a particle size which will at least predominantly pass through a -mesh screen, and should preferably predominantly pass through a 200-mesh screen.
  • the inert carrier material should be added in an amount of at least about 5% by weight of the total napalm formed and should preferably be present in amonut of about 20% by weight of the total napalm formed. Though there is no upper limit on the amount of inert carrier material which may be used, I have found that it is not advisable to use in excess of about 20% by weight with reference to the total napalm formed in that too large a proportional amount of the inert carrier may act as a diluent and necessitate a relatively larger amount of napalm for the gelling of the gasoline.
  • the inert carrier may be added at any point in the process prior to the drying of the napalm, I have found it preferable to add the inert carrier material after filtering the saponified mixtures of the organic acids and prior to the addition of the aluminum sulfate. I have also found it advantageous to add an additional amount of the inert carrier material after the saponified mixture is precipitated by the aluminum sulfate. This additional inert carrier material may be added after the precipitate has been filtered and the filtrate mixed with clean water. At Whatever point the inert carrier is added to the process, it is necessary that the same be thoroughly mixed and dispersed in the reactants.
  • Example 1 25 grams of cocoanut oil fatty acids, 12.5 grams of naphthenic acid and 12.5 grams of oleic acid were melted together and added to 1,600 cc. of water containing 11.5 grams of 95% powdered sodium hydroxide. The solution was heated to F. and stirred for ten minutes. 5 grams of activated carbon were added and the stirring continued for five minutes. The solution was then filtered and the clear filtrate cooled to room temperature. 10 grams of a diatomaceous earth sold under the trade name of Celite were added 3 to the cooled, clear filtrate. 3'7 grams of A12(SO4)318H2O were dissolved in 100 cc. of water and then slowly added to the clear filtrate containing the Celite. A napalm Celite mixture precipitated.
  • This mixture was filtered and transferred to a beaker with clean water and grams more of Celite added with stirring. The mixture was filtered and the filtered cake washed and dried in an oven at C. The dried product obtained was very fine and broke up easily into a fine, uniform, light powder. This fine powdery napalm C'elite mixture proved very excellent for the gelling of gasoline. Conventional amounts will gel aviation gasoline in 23 seconds at F. and five minutes and 55 seconds at 32 F. No additive such as xylenol was needed to aid in the gelling.
  • Example 2 The process as set forth in Example 1 was repeated, using in turn silica gel, talc, activated carbon and alumina.
  • the silica gel and talc produced a napalm composition which was equal in every manner to that formed with the Celite.
  • the alumina and activated carbon each produced a napalm composition superior to that produced by conventional methods and which could be used for gelling gas at temperatures below 0. without the use of xylenol.
  • the product obtained with the use of the carbon black and alumina did not, however, reach the overall excellence of that obtained with the use of Celite silica gel.
  • the napalm treated in the above examples is a napalm produced in the conventional manner with the use of cocoanut oil, fatty acids, naphthenic acids and oleic acids
  • the new process is applicable for use in the production of napalm with any organic acids or variations of the organic acids conventionally used for this purpose.
  • the invention essentially comprises the addition of an inert carrier such as diatomaceous earths, silica gel, activated carbon or alumina having a particle size at least small enough to predominantly pass through a mesh screen and preferably finer to the reactants used in the production of napalm at any point in the process prior to the drying thereof, in amount equal to at least 5% by weight of the napalm formed.
  • an inert carrier such as diatomaceous earths, silica gel, activated carbon or alumina having a particle size at least small enough to predominantly pass through a mesh screen and preferably finer to the reactants used in the production of napalm at any point in the process prior to the drying thereof, in amount equal to at least 5% by weight of the napalm formed.
  • an aluminum soap of a mixture or organic acids selected from cocoanut oil fatty acids, naphthenic acid and oleic acid, adapted on addition to gasoline to cause a gelling thereof which process includes saponifying a mixture of said organic acids with sodium hydroxide, thereby producing a sodium soap of said organic acids, followed by precipitation of the aluminum soap of said organic acids by adding aluminum sulfate to an aqueous solution of said sodium soap, and thereafter drying the said aluminum soap
  • the improvemnt which comprises adding to and dispersing into said materials prior to said drying from 5-20% by weight of the aluminum soap so formed of a finely divided inert carrier having a particle size which will at least predominantly pass through a 100 mesh screen, selected from at least one member of the group consisting of diatomaceous earth, silica gel, talc, activated carbon and alumina, and after said drying recovering a uniform pulverulent aluminum soap.

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  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Engineering & Computer Science (AREA)
  • Fats And Perfumes (AREA)
  • Detergent Compositions (AREA)

Description

Patented July 20, 1954 UNETED eras rare FEE PROCESS OF PREPARING A NAPALM COM- POSITION CONTAENING A FINELY DIVIDED INERT CARRIER No Drawing. Application October 9, 1951, Serial No. 250,560
2 Claims.
This invention relates to improved napalm.
It more particularly relates to an improvement in the process for the production of napalm for saponifying a meltedmixture of cocoanut oil fatty acids, naphthenic acid and oleic acid with a sodium hydroxide solution, precipitating napalm from the saponified mixture by the addition of hydrated aluminum sulfate and drying the napalm precipitate to form the napalm to be used in the gelling of the gasoline.
The napalm produced according to this method is generally not uniform in appearance and usually consists of crumbly and tacky granular particles.
In order to gel gasoline with the napalm, it has been found necessary to heat the gasoline to about 80 F. prior to the napalm addition and to add xylenol to aid in the gelling. The heating of the gasoline is, of course, extremely dangerous and entails a constant hazard of combustion and explosion. The use of xylenol is very undesirable, as it is extremely toxic, corrosive to the skin, and thus very difficult to handle.
A process for grinding this crumbly and tacky napalm in order to overcome these difficulties is described in United States patent application Serial No. 254,437, filed November 1, 1951, now abandoned. In the process described in this application, this tacky and granular napalm which is generally unadaptable for grinding, is ground into a reactive and uniform pulverulent mass. This grinding, however, is not entirely satisfactory, as it involves additional power use, equipment and expense.
One object of this invention is the production of a uniform, finely pulverulent napalm without grinding.
A further object of this invention is a napalm which may be used to gel gasoline in a highly satisfactory manner at any temperature above freezing.
A still further object of this invention is a napalm which may be used to gel gasoline in an excellent manner without the addition of xylenol. These and still further objects will become apparent from the following description:
I have now found that a very uniform and finely powdered napalm may be consistently produced without grinding if an inert carrier material such as diatomaceous earth, talc, silica gel, activated carbon or alumina is added during the production of the napalm at any point in the process prior to the drying.
The inert carrier material should be finely divided and have a particle size which will at least predominantly pass through a -mesh screen, and should preferably predominantly pass through a 200-mesh screen. The inert carrier material should be added in an amount of at least about 5% by weight of the total napalm formed and should preferably be present in amonut of about 20% by weight of the total napalm formed. Though there is no upper limit on the amount of inert carrier material which may be used, I have found that it is not advisable to use in excess of about 20% by weight with reference to the total napalm formed in that too large a proportional amount of the inert carrier may act as a diluent and necessitate a relatively larger amount of napalm for the gelling of the gasoline.
Though the inert carrier may be added at any point in the process prior to the drying of the napalm, I have found it preferable to add the inert carrier material after filtering the saponified mixtures of the organic acids and prior to the addition of the aluminum sulfate. I have also found it advantageous to add an additional amount of the inert carrier material after the saponified mixture is precipitated by the aluminum sulfate. This additional inert carrier material may be added after the precipitate has been filtered and the filtrate mixed with clean water. At Whatever point the inert carrier is added to the process, it is necessary that the same be thoroughly mixed and dispersed in the reactants.
The details of the invention will be more clearly illustrated from the following examples which are given solely for this purpose and are not intended in any way to limit the scope of the invention:
Example 1 25 grams of cocoanut oil fatty acids, 12.5 grams of naphthenic acid and 12.5 grams of oleic acid were melted together and added to 1,600 cc. of water containing 11.5 grams of 95% powdered sodium hydroxide. The solution was heated to F. and stirred for ten minutes. 5 grams of activated carbon were added and the stirring continued for five minutes. The solution was then filtered and the clear filtrate cooled to room temperature. 10 grams of a diatomaceous earth sold under the trade name of Celite were added 3 to the cooled, clear filtrate. 3'7 grams of A12(SO4)318H2O were dissolved in 100 cc. of water and then slowly added to the clear filtrate containing the Celite. A napalm Celite mixture precipitated. This mixture was filtered and transferred to a beaker with clean water and grams more of Celite added with stirring. The mixture was filtered and the filtered cake washed and dried in an oven at C. The dried product obtained was very fine and broke up easily into a fine, uniform, light powder. This fine powdery napalm C'elite mixture proved very excellent for the gelling of gasoline. Conventional amounts will gel aviation gasoline in 23 seconds at F. and five minutes and 55 seconds at 32 F. No additive such as xylenol was needed to aid in the gelling.
Example 2 The process as set forth in Example 1 was repeated, using in turn silica gel, talc, activated carbon and alumina. The silica gel and talc produced a napalm composition which was equal in every manner to that formed with the Celite. The alumina and activated carbon each produced a napalm composition superior to that produced by conventional methods and which could be used for gelling gas at temperatures below 0. without the use of xylenol. The product obtained with the use of the carbon black and alumina did not, however, reach the overall excellence of that obtained with the use of Celite silica gel.
Though the napalm treated in the above examples is a napalm produced in the conventional manner with the use of cocoanut oil, fatty acids, naphthenic acids and oleic acids, the new process is applicable for use in the production of napalm with any organic acids or variations of the organic acids conventionally used for this purpose.
It is thus apparent that the invention essentially comprises the addition of an inert carrier such as diatomaceous earths, silica gel, activated carbon or alumina having a particle size at least small enough to predominantly pass through a mesh screen and preferably finer to the reactants used in the production of napalm at any point in the process prior to the drying thereof, in amount equal to at least 5% by weight of the napalm formed.
I claim:
1. In the process for the production of an aluminum soap of a mixture or organic acids selected from cocoanut oil fatty acids, naphthenic acid and oleic acid, adapted on addition to gasoline to cause a gelling thereof, which process includes saponifying a mixture of said organic acids with sodium hydroxide, thereby producing a sodium soap of said organic acids, followed by precipitation of the aluminum soap of said organic acids by adding aluminum sulfate to an aqueous solution of said sodium soap, and thereafter drying the said aluminum soap, the improvemnt which comprises adding to and dispersing into said materials prior to said drying from 5-20% by weight of the aluminum soap so formed of a finely divided inert carrier having a particle size which will at least predominantly pass through a 100 mesh screen, selected from at least one member of the group consisting of diatomaceous earth, silica gel, talc, activated carbon and alumina, and after said drying recovering a uniform pulverulent aluminum soap.
2. Process according to claim 1 in which at least part of said finel divided inert carrier is added to and dispersed in said materials after said saponification and prior to said precipitation.
References Cited in the file of this patent UNITED STATES PATENTS Number Name Date 704,364 Pefier July 8, 1902 1,968,628 Alton July 31, 1934 2,207,737 Hooft et al. July 16, 1940 2,390,609 Minich Dec. 11, 1945

Claims (1)

1. IN THE PROCESS FOR THE PRODUCTION OF AN ALUMINUM SOAP OF A MIXTURE OF ORGANIC ACIDS SELECTED FROM COCOANUT OIL FATTY ACIDS, NAPHTHENIC ACID AND OLEIC ACID, ADAPTED ON ADDITION TO GASOLINE TO CAUSE A GELLING THEREOF, WHICH PROCESS INCLUDES SAPONIFYING A MIXTURE OF SAID ORGANIC ACIDS WITH SODIUM HYDROXIDE, THEREBY PRODUCING A SODIUM SOAP OF SAID ORGANIC ACIDS, FOLLOWED BY PRECIPITATION OF THE ALUMINUM SOAP OF SAID ORGANIC ACIDS BY ADDING ALUMINUM SULFATE TO AN AQUEOUS SOLUTION OF SAID SODIUM SOAP, AND THEREAFTER DRYING THE SAID ALUMINUM SOAP, THE IMPROVEMENT WHICH COMPRISES ADDING TO AND DISPERSING INTO SAID MATERIALS PRIOR TO SAID DRYING FROM 5-20% BY WEIGHT OF THE ALUMINUM SOAP SO FORMED OF A FINELY DIVIDED INERT CARRIER HAVING A PARTICLE SIZE WHICH WILL AT LEAST PREDOMINANTLY PASS THROUGH A 100 MESH SCREEN, SELECTED FROM AT LEAST ONE MEMBER OF THE GROUP CONSISTING OF DIATOMACEOUS EARTH, SILICA GEL, TALC, ACTIVATED CARBON AND ALUMINA, AND AFTER SAID DRYING RECOVERING A UNIFORM PULVERULENT ALUMINUM SOAP.
US250560A 1951-10-09 1951-10-09 Process of preparing a napalm composition containing a finely divided inert carrier Expired - Lifetime US2684339A (en)

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Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2769697A (en) * 1953-04-29 1956-11-06 Goldenson Jerome Thickener for hydrocarbon fuels
US3239467A (en) * 1962-02-15 1966-03-08 Lord Corp Metal cleaning and treating compositions
US4202668A (en) * 1970-07-15 1980-05-13 The United States Of America As Represented By The Secretary Of The Navy Gelled fuel simulant

Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US704364A (en) * 1901-11-04 1902-07-08 Harry C Peffer Soap.
US1968628A (en) * 1931-07-07 1934-07-31 Vanderbilt Co R T Powdered soap product and method of preparing the same
US2207737A (en) * 1938-07-28 1940-07-16 Lucidol Corp Nonlumping calcium sulphate containing composition
US2390609A (en) * 1942-07-29 1945-12-11 Nuodex Products Co Inc Bodying agent for liquid hydrocarbons

Patent Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US704364A (en) * 1901-11-04 1902-07-08 Harry C Peffer Soap.
US1968628A (en) * 1931-07-07 1934-07-31 Vanderbilt Co R T Powdered soap product and method of preparing the same
US2207737A (en) * 1938-07-28 1940-07-16 Lucidol Corp Nonlumping calcium sulphate containing composition
US2390609A (en) * 1942-07-29 1945-12-11 Nuodex Products Co Inc Bodying agent for liquid hydrocarbons

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2769697A (en) * 1953-04-29 1956-11-06 Goldenson Jerome Thickener for hydrocarbon fuels
US3239467A (en) * 1962-02-15 1966-03-08 Lord Corp Metal cleaning and treating compositions
US4202668A (en) * 1970-07-15 1980-05-13 The United States Of America As Represented By The Secretary Of The Navy Gelled fuel simulant

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