US1056367A - Continuous process for producing explosives. - Google Patents

Continuous process for producing explosives. Download PDF

Info

Publication number
US1056367A
US1056367A US70084612A US1912700846A US1056367A US 1056367 A US1056367 A US 1056367A US 70084612 A US70084612 A US 70084612A US 1912700846 A US1912700846 A US 1912700846A US 1056367 A US1056367 A US 1056367A
Authority
US
United States
Prior art keywords
ingredients
explosives
water
evaporated
solution
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
US70084612A
Inventor
Fritz Raschig
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.)
Individual
Original Assignee
Individual
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 Individual filed Critical Individual
Priority to US70084612A priority Critical patent/US1056367A/en
Application granted granted Critical
Publication of US1056367A publication Critical patent/US1056367A/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C06—EXPLOSIVES; MATCHES
    • C06B—EXPLOSIVES OR THERMIC COMPOSITIONS; MANUFACTURE THEREOF; USE OF SINGLE SUBSTANCES AS EXPLOSIVES
    • C06B31/00—Compositions containing an inorganic nitrogen-oxygen salt
    • C06B31/28—Compositions containing an inorganic nitrogen-oxygen salt the salt being ammonium nitrate
    • C06B31/285—Compositions containing an inorganic nitrogen-oxygen salt the salt being ammonium nitrate with fuel oil, e.g. ANFO-compositions

Definitions

  • fronr a mixture of Water soluble ingredients such as those described in my prior applications, Serial Nos. 690,183 and 690,184 which is both rapid in operation and by means of which the dangers attending such production are minimized; and it comprises a process of .evaporating a solution, containing such a mixture of water soluble ingredients by running such solution in a stream on to a heated moving surface, such as a steam heated, revolving cylinder, whereby almost instantaneous evaporation is etfected, after which the evaporated mass is scraped from the heated surface, all as more fully hereinafter set forth and as claimed.
  • the ingredients used in the novel process of the present invention may be the waste sulfite constituents (lignin snlfonic acids, etc.) and oxygen carriers described in my a J: v prior .applipation, S. N. 690,183, or such aromaticisulfonic acids and oxygen carriers spondingly lower temperature.
  • the sullite waste liquors may be used in their diluted form, or may be eon centrated or evaporated before intermixture or they may be otherwise treated as de scribed in such prior application to give the solution to be evaporated and containing the sulfite Waste constituents together with oxygen carriers.
  • homogeneous intermixture is possible and it is from these homogenous mixtures that the explosives according to the present invention are produced.
  • Aromatic sulfonic acids such as those described in my aforementioned application can also be used according to the process of the present invention, or other aromatic sulfonic acids than those there mentioned.
  • the solutions of the sulfonic acids and oxygen carriers can be produced as more fully described in said prior application to give a solution containing the ingredients from which the explosive is to be obtainedby evaporation.
  • the evaporation of the solutions containing the water soluble ingredients accord ing to the present invention is effected by running such solution in a thin regulated stream onto a heated moving surface.
  • a surface may be a rotating disk or a rotating cylinder internally heated as by steam to a ten'iperature above 100 C.
  • such surface may be placed in a vacuum chamber and the evaporation carried out at a corre-
  • the thin stream as itv runs on to the moving surface is evaporated almost instantaneously. and without danger, and the evaporated product is of a substantially homogeneous nature.
  • the evaporated ribhon-like mass is scraped elf the roller or disk or other heated surface by scrapers or other appliances.
  • the scrapers may advantageously be of bronze or of some other such softer metal.
  • the present invention which is of general ously, and from the cylinder the evaporated ribbon like mass is removed by scrapers 111 a continuous manner, and is the desired explosive.
  • Example 2 87 parts of ammonlum n1 trate and 14 parts of cresol sulfonate of sodium are dissolved and evaporated by .running the solution in a thin stream onto a rotating hollow disk heated internally by steam to a few degrees above 100 C. The evaporated mass is removed as already described and is the desired explosive.
  • Example 3 69 parts of sodium nitrate and 3l parts of cresol sulfonate of sodium are dissolved in watn' and evaporated as above described. 7 is v r r
  • Example 4 70 parts of sodium nitrate and 30 parts of xylenol sulfonate of sodium are treated as above described.
  • oxygen carriers canbe used 6. g.sodium, potassium or ammonium nitrate, chlorates, perchlorates, etc.
  • Example 5 85 parts of nitrate of ammonia are dissolved in waste sulfite liquors containing 15 arts of dry wood. fiber constituents. The liquor is run onto steam heated rollers as already described. T e sulfite liquors can be partly evaporated efore intermixture.
  • Example 6 60v parts of nitrate of ammonia and 30 parts of sulfate of sodium are dissolved in waste sulfite liquors containing 10 parts of wood fiber constituents and evaporated as already described.
  • the sodium sulfate acts as a diluent, but even as so diluted reliable .explosives are obtainable.
  • ammonium nitrate instead of the ammonium nitrate of the foregoing examples, corresponding amounts of sodium or potassium nitrate, or of other oxygen carrier or carriers can be used. Sul fite waste made from other cellulosic material than wood can be similarly employed.
  • the explosives made by the novel evaporation process of the present invention 'con tain the various'ingredients in intimate intermixture and as a result their action is. and substantially complete comdependable, bustion, with a minimum or total absence of smoke, takes place.
  • the process is moreover one in which the danger to the operator is minimized.
  • one of the ingredients may be dissolved in a solution of the other; or a solution of one ingredient may be used to thoroughly moisten or partly dissolve the other, and the resulting solution or partial solution evaporated according to the novel process of the presentinvention.
  • examples can be used as explosives alone, or can be compounded with other explosive ingredients or with modifying or water.- proofing ingredients, and can be formed or molded into a desired form.
  • I claim z- 1. The process of producing explosives water soluble ingredidissolving such ingresubjecting the resultform of a regulated stream to a temperature suflicient to effect substantially instantaneous evaporation.
  • T he process of producing explosives from organic sulfonic acids and oxygen carriers which comprises dissolving such ingredients in water and allowing the resulting solution in the form of a regulated stream to flow on to a continuously moving heated surface.

Landscapes

  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Inorganic Chemistry (AREA)
  • Organic Chemistry (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

Description

EJMTED sra'rns Parana curios.
.FRITZ BASCHIG, OF LUDWiGSHAFEN-ON-THE-BHINE, GERMANY.
CONTINUOUS PROCESS FOR PRODUCING EXPLOSIVES.
N0 Drawing.
Filtfilltfid Mar. 18, 1913..
of a substantially homogeneous nature fronr a mixture of Water soluble ingredients such as those described in my prior applications, Serial Nos. 690,183 and 690,184 which is both rapid in operation and by means of which the dangers attending such production are minimized; and it comprises a process of .evaporating a solution, containing such a mixture of water soluble ingredients by running such solution in a stream on to a heated moving surface, such as a steam heated, revolving cylinder, whereby almost instantaneous evaporation is etfected, after which the evaporated mass is scraped from the heated surface, all as more fully hereinafter set forth and as claimed.
In the production of explosives from a mixture of ingredients it is necessary that an intermixture as nearly homogeneous as possible be obtained if the explosive is to be reliable, and complete combustion thereofis to be effected. With the old dry-mixture process it frequently happens that the intermixture is imperfect and that the explosive as a result incompletely combusts, giving 0E smoke and leaving unburned par ticles. Such explosives are unreliable and erratic in operation, and their production is attended with danger. Again when so lutions are evaporated in order to remove the solvent, continual stirring is required to prevent fractional crystallization or separa tion of the dissolved ingredients. By the process of the present invention, however, the dangers and disadvantages of the old dry mixture process and the old methods of evaporation are minimized, and from a solution containing a plurality of'ingredients an explosive is obtained in. a substantially homogeneous condition.
The ingredients used in the novel process of the present invention may be the waste sulfite constituents (lignin snlfonic acids, etc.) and oxygen carriers described in my a J: v prior .applipation, S. N. 690,183, or such aromaticisulfonic acids and oxygen carriers spondingly lower temperature.
as described in my prior application, S. N. 690,184. The sullite waste liquors may be used in their diluted form, or may be eon centrated or evaporated before intermixture or they may be otherwise treated as de scribed in such prior application to give the solution to be evaporated and containing the sulfite Waste constituents together with oxygen carriers. In these solutions homogeneous intermixture is possible and it is from these homogenous mixtures that the explosives according to the present invention are produced. Aromatic sulfonic acids such as those described in my aforementioned application can also be used according to the process of the present invention, or other aromatic sulfonic acids than those there mentioned. The solutions of the sulfonic acids and oxygen carriers can be produced as more fully described in said prior application to give a solution containing the ingredients from which the explosive is to be obtainedby evaporation.
The evaporation of the solutions containing the water soluble ingredients accord ing to the present invention is effected by running such solution in a thin regulated stream onto a heated moving surface. Such, a surface may be a rotating disk or a rotating cylinder internally heated as by steam to a ten'iperature above 100 C. Or such surface may be placed in a vacuum chamber and the evaporation carried out at a corre- The thin stream as itv runs on to the moving surface is evaporated almost instantaneously. and without danger, and the evaporated product is of a substantially homogeneous nature.
From the heated surface the evaporated ribhon-like mass is scraped elf the roller or disk or other heated surface by scrapers or other appliances. Where iron or steel surfaces are used the scrapers may advantageously be of bronze or of some other such softer metal.
The present invention which is of general ously, and from the cylinder the evaporated ribbon like mass is removed by scrapers 111 a continuous manner, and is the desired explosive. a
Example 2: 87 parts of ammonlum n1 trate and 14 parts of cresol sulfonate of sodium are dissolved and evaporated by .running the solution in a thin stream onto a rotating hollow disk heated internally by steam to a few degrees above 100 C. The evaporated mass is removed as already described and is the desired explosive.
.Example 3: 69 parts of sodium nitrate and 3l parts of cresol sulfonate of sodium are dissolved in watn' and evaporated as above described. 7 is v r r Example 4: 70 parts of sodium nitrate and 30 parts of xylenol sulfonate of sodium are treated as above described.
- Other aromatic sulfonic acids than those mentioned can be used in a similar manner,
6. g. the mono-sulfonic acids of phenol, to
luol, cumol, .cresol, etc, or the disulfonic acids of the above mentioned or other aromatic bodies; or mixtures of two or more of the mono-, or di-or other sulfonic acids.
It is usually more advantageous to use such acids in the form of their water soluble salts. Other oxygen carriers canbe used 6. g.sodium, potassium or ammonium nitrate, chlorates, perchlorates, etc.
Example 5: 85 parts of nitrate of ammonia are dissolved in waste sulfite liquors containing 15 arts of dry wood. fiber constituents. The liquor is run onto steam heated rollers as already described. T e sulfite liquors can be partly evaporated efore intermixture.
Example 6: 60v parts of nitrate of ammonia and 30 parts of sulfate of sodium are dissolved in waste sulfite liquors containing 10 parts of wood fiber constituents and evaporated as already described. The sodium sulfate acts as a diluent, but even as so diluted reliable .explosives are obtainable.
Instead of the ammonium nitrate of the foregoing examples, corresponding amounts of sodium or potassium nitrate, or of other oxygen carrier or carriers can be used. Sul fite waste made from other cellulosic material than wood can be similarly employed.
By the use of a vacuum chamber SL111.-
rounding the heating surfaces on which evaporation takes place it is possible to carry out the evaporation at correspond-- ingly lower temperatures.
The explosives made by the novel evaporation process of the present invention 'con tain the various'ingredients in intimate intermixture and as a result their action is. and substantially complete comdependable, bustion, with a minimum or total absence of smoke, takes place. The process is moreover one in which the danger to the operator is minimized. i
from a plurality of ing solution in the water, one of the ingredients may be dissolved in a solution of the other; or a solution of one ingredient may be used to thoroughly moisten or partly dissolve the other, and the resulting solution or partial solution evaporated according to the novel process of the presentinvention.
The products resulting from the foregoing "examples can be used as explosives alone, or can be compounded with other explosive ingredients or with modifying or water.- proofing ingredients, and can be formed or molded into a desired form.
Variations and modifications can be made in the processes abovedescribed without departing from the spirit and scope of the invention, as set forth in the accompanying claims.
. I claim z- 1. The process of producing explosives water soluble ingredidissolving such ingresubjecting the resultform of a regulated stream to a temperature suflicient to effect substantially instantaneous evaporation.
2. The process of producing explosives from a plurality of water soluble ingredients which comprises dissolving such ingredients in Water and. subjecting the resulting solution in the form of a thin stream to substantially instantaneous evaporation upon a heated surface.
3.- -The process of producing explosives from a plurality of water soluble ingredients which comprises dissolving such ingredients in water and subjecting the resulting solution in the form of a thin stream to temperature above 100 C. to eflect evapora-' tion thereof.
4. The process of producing explosives from a plurality of water soluble ingredients which comprises dissolving such ingredients water and allowing the resulting solution in the form of a regulated stream to flow on to a continuously moving heated surface.
5. The process of producing explosives from a plurality of water soluble ingredients which comprises dissolving such ingreclients in water and allowing the resulting solution in the form of a regulated stream to flow on to a continuously moving heated surface heated by steam to above 100 C.
The process of producing explosives from organic sulfonic acid's and oxygen car-- riers which comprises dissolving such ingredients in water and subjecting the resulting solution in the form of a regulated stream to a temperature suflicient to effect substanents which comprises dleHtS in water and "tially instantaneous evaporation:
solution in the form of a thin stream to substantially instantaneous evaporation upon a heated surface. I
8. The process of producing explosives from organic sulfonic acids and oxygen carriers which comprises dissolving such ingredients in water and subjecting the resulting solution in the form of a thin stream to a temperature above 100 C.
9. T he process of producing explosives from organic sulfonic acids and oxygen carriers which comprises dissolving such ingredients in water and allowing the resulting solution in the form of a regulated stream to flow on to a continuously moving heated surface.
10. The process of producing explosives from organic sulfonic acids and oxygen carriers which comprises dissolving such ingre-' dients in Water and allowing the resulting solution in the form of a regulated stream to flow on to a continuously moving heated surface heated by steam to above 100 C.
11. The process of producing explosives from aromatic sulfonic acids and oxygen carriers which comprises dissolving such ingredients in water and subjecting the resulting solution in the form of a regulated stream to a temperature sufi'icient to efiect substantially instantaneous evaporation.
12. The process of producing explosives from aromatic sulfonic acids and oxygen carriers which comprises dissolving such ingredients in water and subjecting the resulting solution in the form of a thin stream to substantially instantaneous evaporation upon a heated surface.
13. The process of producing explosives from aromatic sulfonic acids and oxygen carriers which comprises dissolving such ingredients in Water and subjecting the resulting solution in the form of a thin stream to a temperature above 100 C.
-14. The process of producing explosives from aromatic sulfonic acids and oxygen carriers which comprises dissolving such ingredients in water and allowing the resulting solution in the form of a regulated stream to flow on to a continuously moving heated surface.
15. The process of producing explosives from aromatic sulfonic acids and oxygen carriers which comprises dissolvin such ingredients in water and allowing t e resulting solution in the form of a regulated stream to flow on to a continuously moving heated surface heated by steam to above 100 C. y
In testimony whereof I have hereunto set my hand in the presence of two subscribing Witnesses.
FRITZ RASOHIG.
Witnesses:
S. H. SHANK, JOSEPH PFEIFFER.
US70084612A 1912-05-31 1912-05-31 Continuous process for producing explosives. Expired - Lifetime US1056367A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
US70084612A US1056367A (en) 1912-05-31 1912-05-31 Continuous process for producing explosives.

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US70084612A US1056367A (en) 1912-05-31 1912-05-31 Continuous process for producing explosives.

Publications (1)

Publication Number Publication Date
US1056367A true US1056367A (en) 1913-03-18

Family

ID=3124621

Family Applications (1)

Application Number Title Priority Date Filing Date
US70084612A Expired - Lifetime US1056367A (en) 1912-05-31 1912-05-31 Continuous process for producing explosives.

Country Status (1)

Country Link
US (1) US1056367A (en)

Similar Documents

Publication Publication Date Title
US2268443A (en) Sulphonation of organic compounds
US2594302A (en) Process for the recovery of valuable constituents from waste sulfite liquor
US2324199A (en) Preparation of ammonium and amine salts of acidic organic compounds
US2277325A (en) Sulphonyl halides
US2200603A (en) Method for the improving of goods
US2109952A (en) Method of preparing aminosulphonic acid
US1547907A (en) Manufacture of wood pulp and by-products
SE8101987L (en) PROCEDURE FOR THE PREPARATION OF REGENERATED CELLULOSA PRODUCTS AND RECOVERY OF THE SOLUTION CHEMICALS
US833634A (en) Process of treating waste sulfite liquor and compound obtained.
US2763531A (en) Manufacture of sodium thiosulphate from sodium sulfite and sulfur in presence of cationic surface active organic bromides
US2401879A (en) Purification of crude trinitrotoluene
US1211923A (en) Method of separating a sulfonic acid of a hydrocarbon of the aromatic series from sulfuric acid and of converting the sulfonic acid into a salt.
US1000487A (en) Art of preparing fatty-acid compounds.
US904483A (en) Process of decolorizing tannin extracts.
US2036997A (en) Process for stabilizing chlorinated rubber
US1109187A (en) Refining petroleum and its by-products.
US1136724A (en) Non-explosive preparations and process of making same.
US2121032A (en) Detergent and wetting agent and process of producing the same
US3133117A (en) Sulfone inhibitors in aromatic sulfonations
US670346A (en) Process of treating nitro-cellulose.
US1423711A (en) Process for obtaining sulphur compounds from mineral oils and the like
US1857520A (en) Purification of sodium acetate
US656263A (en) Process of separating cresols.
US1384219A (en) Process of treating waste liquor from sulfite-cellulose factories
US618809A (en) Henri raymond vidal