US1097145A - Fire-extinguishing compound. - Google Patents

Fire-extinguishing compound. Download PDF

Info

Publication number
US1097145A
US1097145A US75759613A US1913757596A US1097145A US 1097145 A US1097145 A US 1097145A US 75759613 A US75759613 A US 75759613A US 1913757596 A US1913757596 A US 1913757596A US 1097145 A US1097145 A US 1097145A
Authority
US
United States
Prior art keywords
chlorin
carbon
chlorid
fire extinguishing
compound
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired - Lifetime
Application number
US75759613A
Inventor
Walter O Snelling
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
FRANK L DYER
JONAS W AYLSWORTH
Original Assignee
FRANK L DYER
JONAS W AYLSWORTH
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by FRANK L DYER, JONAS W AYLSWORTH filed Critical FRANK L DYER
Priority to US75759613A priority Critical patent/US1097145A/en
Application granted granted Critical
Publication of US1097145A publication Critical patent/US1097145A/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Classifications

    • AHUMAN NECESSITIES
    • A62LIFE-SAVING; FIRE-FIGHTING
    • A62DCHEMICAL MEANS FOR EXTINGUISHING FIRES OR FOR COMBATING OR PROTECTING AGAINST HARMFUL CHEMICAL AGENTS; CHEMICAL MATERIALS FOR USE IN BREATHING APPARATUS
    • A62D1/00Fire-extinguishing compositions; Use of chemical substances in extinguishing fires
    • A62D1/0028Liquid extinguishing substances
    • A62D1/0057Polyhaloalkanes

Definitions

  • carbon tetrachlorid is a valuable and efficient fire extinguishing material, and for a number of years several types of fire extinguisher have been on the market in which it is used as an ingredient.
  • Carbon tetra-chlorid has however one pronounced disadvantage for this purpose, in that it exerts a marked corrosive action-upon certain metals, particularly brass and similar alloys, when kept for a considerable time in metallic containers. Bepause of this action stop-cocks orvalves attached to fire extinguishing apparatus in which carbon tetra-chlorid is used tend tobecome clogged.
  • a fire extinguishing device should, of course, be instantaneously ready for use when required by the outbreak of fire, and hence the cor-v rosive action of carbon-tetra-chlorid' upon metals and alloys has "greatly decreased its usefulness, resulting inthe necessity of frequent inspections and replenishment of the material and failure of the apparatus at critical times when such watchfulne'ss has not been observed.
  • the unsaturated aliphatic hydrocarbons referred to are the class of substances which I consider best adapted for addition to the carbon tetra-chlorid, that is to say,
  • the material added to the carbon tetrachlorid is one which has' such an affinity for chlorin that it will combine with free chlorin or chlorin dissolved in carbon tetrachlorid, but does not have such aflinity for chlorin that it will breakup carbon tetrachlorid, or will take chlorineout of a stable chlorin compound.
  • the unsaturated aliphatic hydrocarbons or derivatives, particu- I liarly referred to above, responds to this test.
  • the addition of whatever hydro-car- I bon is used is preferably in a small amount, of say from per cent. to 3 per cent.
  • hydrocarbons that take up chlorin or a halogen to form substitution products are not desirable for my purpose, slnce they would set free hydrochloric acid.
  • Many hydrocarbons outside the classes mentioned can, by the use of sufiiciently violent means, be chlorinated, but the hydrocarbons which will answer the requirements of-my invention, '5.
  • Such materials are for example, 'di-chlor-ethylene and tri-chlor-ethylene.
  • fire extinguishing compounds comprising carbon-tetra-chlorid in which is dissolved or commingled halogen substitution products of hydrocarbons containingtwo or .more carbon atoms in the molecule, which poly-halogen compounds are added for the purpose ofraising the boiling point of the material above that of carbon tetra-chlorid alone and forming heavy vapors that are not readily dispersed by the heated gases arising from the burning materials. To attain t is result a greater proportion of the added material is necessary than'is required to attain the purpose of my resent invention.
  • my invention is not limited strictly to the; use with carbon tetra-chl'orid of substances having the effects specified, but that it is broad enough to cpver fire extinguishing compounds m wh ch halogenated .compounds are used, other than carbon 'tetra-chlorid, in which there is a tendenc to decomposition with the setting free of c lorin. In all such cases the unsaturated hydrocarbons added by ,me will render the compound non-cor rosive, as stated.
  • the preferred embodiment of my invention carbon tetra-chlorid and one of the unsaturated hydrocarbonsreferred to.
  • a fire extinguishing compound comprising carbon tetra-chlorid and an unsate nrated hydrocarbon having the property of combining readily with free chlorin.
  • a fire extinguishing compound com-' prising a halogenated hydrocarbon fire extinguishing material having the tendency to partially decompose with the consequent libpartially decompose with the consequent liberation of part of the halogen, and a material which has such an aflinity for the free halogen that it will combine with the same in a 'free state, to form a compound which is noncorrosive to metals, but has not such an affinity for the halogen that it will break down the said halogenated material, or take halogen out of a stable halogen compound.
  • a fire extinguishing compound comprising carbon tetra-chlorid and a material which has such an aifinity for chlorin that it will combine with free chlorin or chlorin dissolved in carbon tetra-chlorid to form a that it will break down carbon tetra-chlorid,
  • a fire extinguishing compound comprising a halogenated fire extinguishing material and a substance which has the propprising carbon tetra-chlorid and an unsaturated hydrocarbon having the property of combining readily with free chlorin the said hydrocarbon being present in the proportion of not more than threeper cent. of the carbon tetra-chlorid, by we ght.
  • a fire extinguishing compound consisting of a halogenated fire extinguishing material and an unsaturated aliphatic hydrocarbon in the proportion of not more than three per cent. of the said fire extinguishing material by weight, which hydrocarbon has the property of combining readily with free corrosive to metals.
  • a fire extinguishing compound consisting of a halogenated fire extinguishing mahalogento form a compound which is nonterial, and a chain hydrocarbon containing two or more doubly-or-trebly-linked carbon atoms, and having the property of combining readily with free halogen to form a compound which is non-corrosive to metals.
  • a fire extinguishing compound consisting of a halogenated fire extinguishing material in combination with a material having the ability to unite with any halogen set free from said halogenated fire extinguishing material to form addition products which are permanently non-corrosive to metals.
  • a fire extinguishing compound consisting of a hologenated fire extinguishing material and an unsaturated aliphatic hydrocarbon containing doubly or trebly linked carbon atoms, capable of uniting under the conditions present in a metallic container, at room temperature, with free chlorin or hydro-chloric acid set free from said hologenated material to form a compound which is'non-corrosive to metals.
  • a fire extinguishing compound comprising carbon tet-ra-chlorid and an unsaturated hydrocarbon of the ethylene series, the said hydrocarbon having the property of combining readily with free chlorin.

Description

M nna" onricn- WALTER- o SNELLING, or PITTSBURGH, PENNSYLVANIA, ASSIGNOR or ONEHALF To FRANK L. DYER, or MoNToLAm, NEW JERSEY, AND JONAS W. AYLSWORTH, OF
EAST ORANGE, NEW JERSEY.
rmE-ExTI GuIsHINs COMPOUND.
No Drawing.
to produce an improved composition of this character in which certain defects,,particularly the corrosive action of such compounds upon brass and other metals, will be obviated.
It is well known, that carbon tetrachlorid is a valuable and efficient fire extinguishing material, and for a number of years several types of fire extinguisher have been on the market in which it is used as an ingredient. Carbon tetra-chlorid has however one pronounced disadvantage for this purpose, in that it exerts a marked corrosive action-upon certain metals, particularly brass and similar alloys, when kept for a considerable time in metallic containers. Bepause of this action stop-cocks orvalves attached to fire extinguishing apparatus in which carbon tetra-chlorid is used tend tobecome clogged. .A fire extinguishing device should, of course, be instantaneously ready for use when required by the outbreak of fire, and hence the cor-v rosive action of carbon-tetra-chlorid' upon metals and alloys has "greatly decreased its usefulness, resulting inthe necessity of frequent inspections and replenishment of the material and failure of the apparatus at critical times when such watchfulne'ss has not been observed.
The corrosive action of carbon tetrachlorid is due to the fact that it partially decomposes when left standin' for a considerable time, and liberatesc lorin, which attacks the brass or other metal of the container within which it is kept'. I havefound that this action may be entirely prevented by adding to the carbon tetrachlorid certain chemical agents whichhave such as various members of the acetylene I Specification of Letters Patent.
Application filed Marc1r29, 1913. Serial No. 757,596. i
Patented as 19, 1914.
and ethylene series of hydrocarbons, when added to carbon tetra-chlorid, take up the small amounts of chlorin or chlorin compounds which are set free by the decomposition of carbon tetra-chlorid and thus prevent this chlorin from exerting a corrosive action upon the metal of the container. In addition to unsaturated hydrocarbons, I
. also find that certain other chemical bodies which have an affinity for chlorin can be used to prevent corrosive action by carbon tetra-chlorid. I find, for example, that an alkaline metal, such as sodium, or a metal of the alkaline earths, either as the free metal or in an alloy or an amalgam, will also serve to prevent corrosive action by carbon tetra-chlorid. v
The unsaturated aliphatic hydrocarbons referred to are the class of substances which I consider best adapted for addition to the carbon tetra-chlorid, that is to say,
of one of these substances, added preferably in a small amount to the carbon tetrachlorid, is to readily take up the free chlorin to form stable addition products.
In the preferred form of my invention,v the material added to the carbon tetrachlorid is one which has' such an affinity for chlorin that it will combine with free chlorin or chlorin dissolved in carbon tetrachlorid, but does not have such aflinity for chlorin that it will breakup carbon tetrachlorid, or will take chlorineout of a stable chlorin compound. 'The unsaturated aliphatic hydrocarbons or derivatives, particu- I liarly referred to above, responds to this test. The addition of whatever hydro-car- I bon is used is preferably in a small amount, of say from per cent. to 3 per cent. by weight of the carbon tetra-chlorid.- I have found that this small amount is suflicient for the desired purpose, and a greater amount 10() is in some instances undesirable; If acetylene, for example, is the substance added to take-up free chlorin, anjexcess of the same will of course be objectionable, since it isinflammable. Alkaline metals, such as sodium,
and the like, referred to above, are not as desirable for addition; to carbon "tetrachlorid as the unsaturated hydro-carbons described, since they do not fully respond to the test given above for the preferred form. of my invention. Sodiumnot only takes up free chlorin, but it also takes chlorin in small amounts directly. from the carbon tetra-chlorid.
As stated, the unsaturated hydrocarbons,
one of which, in the preferred form of my invention, should be used, should be aliphatic or chain hydrocarbons, or derivatives thereof, each of which contains two or more doubly or trebly linked carbon atoms, and which, therefore, has the ability to take up chlorin to form addition products. Hydrocarbons that take up chlorin or a halogen to form substitution products are not desirable for my purpose, slnce they would set free hydrochloric acid. Many hydrocarbons outside the classes mentioned can, by the use of sufiiciently violent means, be chlorinated, but the hydrocarbons which will answer the requirements of-my invention, '5. .e., those that will take up chlorin under ordinar conditions of temperature, and in the dar r, and in the absence of catalyzers, are apparently strictly limited to the aliphatic unsaturated hydrocarbons. My invention accordingly contemplates, in its preferred form, the use of any aliphatic unsaturated hydrocarbon which will take up chlorin under the conditions resent in a bottle or container of fir'e-extmguishing material, as stated.
Of the classes of compounds especially referred to. b me as desirable, good examples of desira 1e members may be given, for
purposes of illustration, as follows: Of the olefin series: symmetrical di-methyl-ethylene,
OH CH=OH-CH Of the acetylene seriesz crotonylene,
CH,C;= OOH,. And of the diolefin series: divinyl,
on,.=on-on=on,.
hydrocarbon of the ethylene series, um'
saturated aliphatic hydrocarbon, 'etc., in the-claims, are to be understood as intended to include such derivatives of such bodies as are the equivalents thereof for the purposes of this invention.
Some of the materials which I propose to add to the carbon tetra-chlorid or other halogenated substance, would have the effect,-'-if"added in considerable quantity, to
raise the boiling point of the mixture. Such materials, are for example, 'di-chlor-ethylene and tri-chlor-ethylene. For the purposes of the present invention, I do not contemplate adding such materials in sufficient proportion to attain this result, and to practice m present invention it is not necessary to a d such material in sufiicient proportion to raise the boiling point of the mixture to any noticeable extent. In my application Ser. No. 702,195, filed June], 1912, I describe fire extinguishing compounds comprising carbon-tetra-chlorid in which is dissolved or commingled halogen substitution products of hydrocarbons containingtwo or .more carbon atoms in the molecule, which poly-halogen compounds are added for the purpose ofraising the boiling point of the material above that of carbon tetra-chlorid alone and forming heavy vapors that are not readily dispersed by the heated gases arising from the burning materials. To attain t is result a greater proportion of the added material is necessary than'is required to attain the purpose of my resent invention. Some of the added su stances mentioned in my previous application I have for example, as acetylene, which may be utilized in small proportions in my,.present invention. When it is desired to attain the useful results of both inventions, some of the poly-halogen hydrocarbon compoimds of my former invention, referred to, may be added to the compound of the present invention, in sufiicient proportion.
It should be understood, that my invention is not limited strictly to the; use with carbon tetra-chl'orid of substances having the effects specified, but that it is broad enough to cpver fire extinguishing compounds m wh ch halogenated .compounds are used, other than carbon 'tetra-chlorid, in which there is a tendenc to decomposition with the setting free of c lorin. In all such cases the unsaturated hydrocarbons added by ,me will render the compound non-cor rosive, as stated. The preferred embodiment of my invention, however, carbon tetra-chlorid and one of the unsaturated hydrocarbonsreferred to.
Having now described my invention, what I cla m and desire to protect by Letters Patentis as follows l. A fire extinguishing compound comprising carbon tetra-chlorid and an unsate nrated hydrocarbon having the property of combining readily with free chlorin.
2. A fire extinguishing compound com-' prising a halogenated hydrocarbon fire extinguishing material having the tendency to partially decompose with the consequent libpartially decompose with the consequent liberation of part of the halogen, and a material which has such an aflinity for the free halogen that it will combine with the same in a 'free state, to form a compound which is noncorrosive to metals, but has not such an affinity for the halogen that it will break down the said halogenated material, or take halogen out of a stable halogen compound.
4. A fire extinguishing compound comprising carbon tetra-chlorid and a material which has such an aifinity for chlorin that it will combine with free chlorin or chlorin dissolved in carbon tetra-chlorid to form a that it will break down carbon tetra-chlorid,
v or take chlorin out of a stable chlorin compound. i
5. A fire extinguishing compound comprising a halogenated fire extinguishing material and a substance which has the propprising carbon tetra-chlorid and an unsaturated hydrocarbon having the property of combining readily with free chlorin the said hydrocarbon being present in the proportion of not more than threeper cent. of the carbon tetra-chlorid, by we ght.
7. A fire extinguishing compound consisting of a halogenated fire extinguishing material and an unsaturated aliphatic hydrocarbon in the proportion of not more than three per cent. of the said fire extinguishing material by weight, which hydrocarbon has the property of combining readily with free corrosive to metals.
8. A fire extinguishing compound consisting of a halogenated fire extinguishing mahalogento form a compound which is nonterial, and a chain hydrocarbon containing two or more doubly-or-trebly-linked carbon atoms, and having the property of combining readily with free halogen to form a compound which is non-corrosive to metals.
9. A fire extinguishing compound consisting of a halogenated fire extinguishing material in combination with a material having the ability to unite with any halogen set free from said halogenated fire extinguishing material to form addition products which are permanently non-corrosive to metals.
10, A fire extinguishing compound consisting of a hologenated fire extinguishing material and an unsaturated aliphatic hydrocarbon containing doubly or trebly linked carbon atoms, capable of uniting under the conditions present in a metallic container, at room temperature, with free chlorin or hydro-chloric acid set free from said hologenated material to form a compound which is'non-corrosive to metals. 1
11. A fire extinguishing compound comprising carbon tet-ra-chlorid and an unsaturated hydrocarbon of the ethylene series, the said hydrocarbon having the property of combining readily with free chlorin.
This specification signed and witnessed this 25th day of March, 1913.
WALTER O. SNELLING.
Witnesses:
C. R. KERR,
GEORGE SCHULER.
US75759613A 1913-03-29 1913-03-29 Fire-extinguishing compound. Expired - Lifetime US1097145A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
US75759613A US1097145A (en) 1913-03-29 1913-03-29 Fire-extinguishing compound.

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US75759613A US1097145A (en) 1913-03-29 1913-03-29 Fire-extinguishing compound.

Publications (1)

Publication Number Publication Date
US1097145A true US1097145A (en) 1914-05-19

Family

ID=3165351

Family Applications (1)

Application Number Title Priority Date Filing Date
US75759613A Expired - Lifetime US1097145A (en) 1913-03-29 1913-03-29 Fire-extinguishing compound.

Country Status (1)

Country Link
US (1) US1097145A (en)

Cited By (14)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2563171A (en) * 1949-10-12 1951-08-07 Jr Charles K Huthsing Apparatus for controlling corrosion in fire extinguishers
US2578529A (en) * 1947-09-19 1951-12-11 Pyrene Mfg Co Fire extinguisher
US2578528A (en) * 1946-10-15 1951-12-11 Pyrene Mfg Co Fire extinguisher
US2658930A (en) * 1949-03-22 1953-11-10 Universal Oil Prod Co Production of polyhaloalkanes
US2775624A (en) * 1953-09-25 1956-12-25 Diamond Alkali Co Stabilized tetrachloroethylene
US2803676A (en) * 1954-04-20 1957-08-20 Dow Chemical Co Trichloroethylene stabilized with propargyl alcohol and pyrrole
US2841625A (en) * 1956-02-08 1958-07-01 Air Reduction Stabilization of chlorinated hydrocarbons with 2, 5-dimethyl-1, 5-hexadiene-3-yne andsynergistic mixtures containing same
US2868851A (en) * 1954-07-26 1959-01-13 Diamond Alkali Co Stabilization of chlorinated hydrocarbons with acetylenic ethers
US2870094A (en) * 1955-09-28 1959-01-20 Eastman Kodak Co Photographic film cleaning solutions
US2958711A (en) * 1954-07-26 1960-11-01 Diamond Alkali Co Stabilization of chlorinated hydrocarbons with carboxylic acid esters of acetylenic alcohols
US2958709A (en) * 1958-05-21 1960-11-01 Diamond Alkali Co Stabilization of metal contaminated chloromethyl benzenes
US2979538A (en) * 1958-07-21 1961-04-11 Diamond Alkaii Company Propynyl esters of dicarboxylic acids for stabilizing halogenated hydrocarbon
US3052734A (en) * 1958-10-27 1962-09-04 Diamond Alkali Co Halogenated aromatic hydrocarbons stabilized with polyacetylenic hydrocarbons
US3291745A (en) * 1963-04-29 1966-12-13 Du Pont Stabilization of trichlorethylene

Cited By (14)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2578528A (en) * 1946-10-15 1951-12-11 Pyrene Mfg Co Fire extinguisher
US2578529A (en) * 1947-09-19 1951-12-11 Pyrene Mfg Co Fire extinguisher
US2658930A (en) * 1949-03-22 1953-11-10 Universal Oil Prod Co Production of polyhaloalkanes
US2563171A (en) * 1949-10-12 1951-08-07 Jr Charles K Huthsing Apparatus for controlling corrosion in fire extinguishers
US2775624A (en) * 1953-09-25 1956-12-25 Diamond Alkali Co Stabilized tetrachloroethylene
US2803676A (en) * 1954-04-20 1957-08-20 Dow Chemical Co Trichloroethylene stabilized with propargyl alcohol and pyrrole
US2958711A (en) * 1954-07-26 1960-11-01 Diamond Alkali Co Stabilization of chlorinated hydrocarbons with carboxylic acid esters of acetylenic alcohols
US2868851A (en) * 1954-07-26 1959-01-13 Diamond Alkali Co Stabilization of chlorinated hydrocarbons with acetylenic ethers
US2870094A (en) * 1955-09-28 1959-01-20 Eastman Kodak Co Photographic film cleaning solutions
US2841625A (en) * 1956-02-08 1958-07-01 Air Reduction Stabilization of chlorinated hydrocarbons with 2, 5-dimethyl-1, 5-hexadiene-3-yne andsynergistic mixtures containing same
US2958709A (en) * 1958-05-21 1960-11-01 Diamond Alkali Co Stabilization of metal contaminated chloromethyl benzenes
US2979538A (en) * 1958-07-21 1961-04-11 Diamond Alkaii Company Propynyl esters of dicarboxylic acids for stabilizing halogenated hydrocarbon
US3052734A (en) * 1958-10-27 1962-09-04 Diamond Alkali Co Halogenated aromatic hydrocarbons stabilized with polyacetylenic hydrocarbons
US3291745A (en) * 1963-04-29 1966-12-13 Du Pont Stabilization of trichlorethylene

Similar Documents

Publication Publication Date Title
US1097145A (en) Fire-extinguishing compound.
WO2012034492A1 (en) Ferrocene-based fire extinguishing composition
FR2362186A1 (en) PLASTICIZED COMPOSITION OF POLYVINYL RESIN CONTAINING AN INFLAMMATION-DELAYING AND MOLYBDENE-BASED FUME-DELAYING AGENT
NO142339B (en) CONTAINER COMPONENT OF METAL PLATE MATERIAL
US2653130A (en) Fire extinguishing composition of cbrf or cfbrcfbr containing cf as a propellant
US2559580A (en) Stabilization of aqueous amine solutions against oxidation and corrosion in gas separation processes
US2721883A (en) Stabilization of halogenated hydrocarbons
Fraser Break the Flame Chain Reaction
US2639221A (en) Noncaking sodium and potassium hydroxide for photographic developer powders
US2493427A (en) Stabilization of halogenated organic compounds
US1895692A (en) Fire extinguishing composition
US1411422A (en) Lachrymatory gas
US1917073A (en) Method of stabilizing chlorinated aliphatic hydrocarbons
US1966881A (en) Industrial liquid
US1895691A (en) Fire extinguisher
US3985658A (en) Extinguishing agent for combustible metal fires
US2211468A (en) Liquid coating for gas filtering mediums
US1891673A (en) Fire extinguishing compound
US278315A (en) Gustave j
US1792826A (en) Fire-extinguishing material
FI78239B (en) HOEGEFFEKTIVA, BRANDFOERDROEJANDE OCH ELDSLAECKANDE PULVER OCH DERAS ANTIKATYTYTIKA TILLSATSAEMNEN.
Baratov et al. About substitution for ozone-depleting agents for fire extinguishing
US1103092A (en) Compound for extinguishing fires.
US1316191A (en) And james m
US3002028A (en) Stable solvent composition