US3511726A - Slurried ammonium nitrate explosive composition containing a chrome-lignin - Google Patents

Slurried ammonium nitrate explosive composition containing a chrome-lignin Download PDF

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Publication number
US3511726A
US3511726A US812849A US3511726DA US3511726A US 3511726 A US3511726 A US 3511726A US 812849 A US812849 A US 812849A US 3511726D A US3511726D A US 3511726DA US 3511726 A US3511726 A US 3511726A
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United States
Prior art keywords
lignin
ammonium nitrate
chrome
explosive composition
slurry
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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
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US812849A
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English (en)
Inventor
Jiro Okabe
Yasuo Yamanaka
Yoshikazu Wakazono
Terushige Ogawa
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Sanyo Pulp Co Ltd
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Sanyo Pulp Co Ltd
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    • CCHEMISTRY; METALLURGY
    • C06EXPLOSIVES; MATCHES
    • C06BEXPLOSIVES OR THERMIC COMPOSITIONS; MANUFACTURE THEREOF; USE OF SINGLE SUBSTANCES AS EXPLOSIVES
    • C06B31/00Compositions containing an inorganic nitrogen-oxygen salt
    • C06B31/28Compositions containing an inorganic nitrogen-oxygen salt the salt being ammonium nitrate
    • C06B31/30Compositions containing an inorganic nitrogen-oxygen salt the salt being ammonium nitrate with vegetable matter; with resin; with rubber

Definitions

  • a slurry lignin explosive composition having a plastic property and a high density which comprises, as its principalingredients, (1) chrome-lignin prepared from spent liquor of sulfite pulp manufacture and a water-soluble, hexavalent chromium compound and (2) ammonium nitrate.
  • This invention relates to relatively inexpensive slurry explosive compositions having characteristic in plastic property and high density and, more particularly, relates to slurry lignin explosive composition having high practical value whose principal ingredients are chrome-lignin and ammonium nitrate.
  • slurry explosive as a commercial explosive composition, which is prepared by suspending ammonium nitrate in water in slurry state and admixing therewith aluminum powder or TNT as a sensitizer and paste of carboxymethylcellulose as a thickener has drawn public attention in the field of explosive.
  • An object of the present invention is to provide a very inexpensive, and safety explosive composition having a suflicient plasticity and a high density for charging in drilled holes and holding detonating property without containing any sensitizer.
  • the abovementioned object can be attained by the composition of the present invention.
  • the composition of the present invention which has the same performance as that of the conventional slurry explosive, can be produced by using chrome-lignin in place of a sensitizer used in the conventional slurry explosive at as low a cost as that of the ANFO explosive.
  • Chromelignin used in the composition of the present invention is a water-insoluble gel substance which is a reaction product between the spent liquor of sulfite pulp and hexavalent water-soluble chromium compounds.
  • the product of this invention is a homogeneous, gel
  • composition obtained -by mixing ammonium nitrate and an aqueous chrome-lignin solution which is not yet gelated, adding, if necessary, a thickener, stirring the mixture sufficiently, and allowing the mixture to stand to gelate the chrome-lignin.
  • Ammonium nitrate may be either of prill or powder form and even ammonium nitrate for agricultural grade may be used.
  • a portion of ammonium nitrate can be displaced by one of the publicly known oxidants, such as other nitrates and perchlorates.
  • ammonium nitrate incorporated in the composition amounts to about 50 to by weight of the explosive composition.
  • the water-soluble, hexavalent chromium compounds such as sodium bichromate, potassium chromate, and chromic anhydride
  • the water-soluble, hexavalent chromium compounds are added to the spent liquor in an amount of 10 to 30% by weight based upon the solid matter in the spent liquor.
  • Other metal salts publicly known such as those having the activity for promoting gel formation may also be added.
  • the aqueous chrome-lignin solution prior to gelation is added desirably in an amount of 10 to 50% by weight based upon the explosive composition.
  • the thickener is added if necessary, and it may be a water-soluble high molecular substance, such as polyvinyl alcohol, polyethylene oxide, salt of polyacrylic acid, or polyacrylamide; a water-soluble polysaccharide derivative, such as carboxymethylcellulose, hydroxyethylcellulose, methylcellulose, guar gum, locust bean gum, or carboxymethylated starch; and mixtures thereof.
  • a publicly known gelation-accelerator such as borax may be used in combination with a thickener.
  • the gelled chrome-lignin in this invention acts also as a thickener, the addition of another thickener is not always necessary. However, the addition of another thickener in a small amount can produce a fluid, extremely stable explosive composition.
  • Ammonium nitrate, an aqueous chrome-lignin solution, and a thickener which is added by necessity can be mixed in any order. After a thick slurry of ammonium nitrate or a thickener solution is prepared, in advance, by using a portion of water of the aqueous chrome-lignin solution, mixing can be carried out. Heat can be employed when they are mixed.
  • the water-soluble hexavalent chromium compounds to be added for the preparation of chrome-lignin may be added in divided portions.
  • the water-soluble hexavalent chromiuum compounds added together with the spent liquor of sulfite pulp manufactur are caused to react mainly with the salt of lignosulfonic acid to lead water-soluble salt of the lignosulfonic acid to form macromolecules, by chelate bonding, which is thus insolubilized. Therefore, the water-soluble hexavalent chromium compounds, which have been added to spent liquor, do not exist in the free form after the gel formation of lignosulfonates. In this point the composition of the present invention is clearly dillerent from conventional ammonium nitrate ex plosive compositions incorporated with potassium bichromate.
  • composition of the present invention is also entirely different from the explosive with a low density and no water-resistant property, described in the specification of East German Patent No. 23657, which comprises the powder obtained from spent liquor of sulfite pulp manufacture, and ammonium nitrate powder, in which the above-mentioned powder from spent liquor of sulfite pulp manufacture is used simply in place of the fuel oil of the ANFO explosive.
  • EXAMPLE 1 A thickener was prepared by dissolving g. of guar gum into 150 g. of water. To this solution, 700 g. of crushed ammonium nitrate of agricultural grade was added. As chrome-lignin a mixture of 120 g. of 40% Sangrout AS solution (a lignin product useful as soil stabilizer, supplied from Sanyo Pulp Co., Ltd., Japan) and 25 g. of 40% aqueous sodium bichromate solution was used. The chrome-lignin solution was mixed with the above-mentioned ammonium nitrate slurry at 40 C. and the mixture was allowed to stand at room temp rature for about 4 hours. Thus, 1 kg. of a homogeneous, slurry lignin explosive composition was obtained. The product had a density of 1.25 g./cc.
  • EXAMPLE 2 A thickener was prepared by dissolving 5 g. of Sunrose SN-30A (carboxymethylcellulose, supplied from Sanyo Pulp Co., Ltd., Japan) and 5 g. of guar gum in 145 g. of water. To this solution was added 700 g. of ammonium nitrate of agricultural grade. As a chrome-lignin a mixture of 120 g. of 40% solution of San X 501 (a lignin product supplied from Sanyo Pulp Co., Ltd., Japan) and 25 g. of 40% aqueous potassium bichromate solution was used. The chrome-lignin solution was mixed with the above mentioned ammonium nitrate slurry at 70 C. and the mixture was allowed to stand for about 24 hours. Thus, 1 kg. of a homogeneous, slurry lignin explosive composition was obtained. The product had a density of 1.22 g./cc.
  • EXAMPLE 3 Fifteen grams of guar gum was dissolved in 145 g. of water, and 650 g. of ammonium nitrate of agricultural grade was added thereto. As a chrome-lignin a mixture of 140 g. of 40% solution of Sangrout AS and 20 g. of 40% aqueous sodium bichromate solution was used. Resultant solution was mixed with the above-mentioned ammonium nitrate slurry at room temperature, and then 30 g. of aluminum powder was added to the mixture. After sufficiently stirred, the mixture was allowed to stand for about 24 hours. Thus, 1 kg. of a homogeneous, slurry lignin explosive composition was obtained. The product had a density of 1.12 g./cc.
  • Example 1 The procedures of Example 1 were repeated by substituting sodium nitrate in Example 4 and sodium perchlorate in Example 5 for the one-third amount of ammoniurn nitrate of Example 1, respectively, and by substituting polyvinyl alcohol (PVA-117, supplied from Kurashiki Rayon Co.) in Example 6, polyethylene oxide (PEG-l8, supplied from Seitetsu Kagaku Co.) in Example 7, polysodium-acrylate (Alon A20P, supplied from Toa Gosei Co.) in Example 8, polyacryl-amide (Nitto SS, Nitto Kagaku Co.) in Example 9, hydroxy-ethyl cellulose (Nisso-HEC AL-15 supplied from Nihon Soda Co.) in Example 10, methyl cellulose (Marpolose M- 400, supplied from Matsu-moto Yushi Co.) in Example 11 and locust bean gum (Meyprog
  • a slurry lignin explosive composition having a plastic property and a high density which comprises, as its principal ingredients, (1) a chrome-lignin prepared by reacting spent liquor of sulfite pulp manufacture with a water-soluble, hexavalent chromium compound, and (2) ammonium nitrate.

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  • Chemical & Material Sciences (AREA)
  • Inorganic Chemistry (AREA)
  • Organic Chemistry (AREA)
  • Treatment Of Sludge (AREA)
  • Processing Of Solid Wastes (AREA)
  • Paper (AREA)
US812849A 1968-04-09 1969-04-02 Slurried ammonium nitrate explosive composition containing a chrome-lignin Expired - Lifetime US3511726A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP2317468 1968-04-09

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US3511726A true US3511726A (en) 1970-05-12

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US (1) US3511726A (enrdf_load_stackoverflow)
DE (1) DE1915456C3 (enrdf_load_stackoverflow)
GB (1) GB1225205A (enrdf_load_stackoverflow)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN106748590A (zh) * 2016-12-21 2017-05-31 四川雅化实业集团股份有限公司 一种粘性炸药用粘合剂及其制备方法
RU2789321C2 (ru) * 2021-07-15 2023-02-01 Федеральное государственное автономное образовательное учреждение высшего образования «Дальневосточный федеральный университет» (ДВФУ) Водосодержащее взрывчатое вещество

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
NO165185C (no) * 1984-12-27 1991-01-09 Aerojet General Co Stoepbar sprengstoffblanding.
US5034073A (en) * 1990-10-09 1991-07-23 Aerojet General Corporation Insensitive high explosive

Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3166450A (en) * 1961-05-01 1965-01-19 Commercial Solvents Corp Ammonium nitrate-chromate salt explosive compositions
US3326733A (en) * 1966-08-15 1967-06-20 Kelco Co Gelled explosive composition containing a xanthamonas hydrophilic colloid
US3361604A (en) * 1966-07-25 1968-01-02 Trojan Powder Co Explosive slurries containing an inorganic oxidizer salt and particulate fibrous naturally wet pulpy plant matter
US3369945A (en) * 1965-11-01 1968-02-20 Canadian Ind Explosive composition containing an inorganic oxidizer salt,a soluble lignosulphonate,and mutual solvent therefor
US3397096A (en) * 1966-12-06 1968-08-13 Canadian Ind Thickened inorganic oxidizer salt explosive slurry sensitized with a soluble polyflavonoid
US3400026A (en) * 1967-01-16 1968-09-03 Du Pont Thickened aqueous inorganic oxidizer salt explosive composition containing dissolvedproteinaceous material

Patent Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3166450A (en) * 1961-05-01 1965-01-19 Commercial Solvents Corp Ammonium nitrate-chromate salt explosive compositions
US3369945A (en) * 1965-11-01 1968-02-20 Canadian Ind Explosive composition containing an inorganic oxidizer salt,a soluble lignosulphonate,and mutual solvent therefor
US3361604A (en) * 1966-07-25 1968-01-02 Trojan Powder Co Explosive slurries containing an inorganic oxidizer salt and particulate fibrous naturally wet pulpy plant matter
US3326733A (en) * 1966-08-15 1967-06-20 Kelco Co Gelled explosive composition containing a xanthamonas hydrophilic colloid
US3397096A (en) * 1966-12-06 1968-08-13 Canadian Ind Thickened inorganic oxidizer salt explosive slurry sensitized with a soluble polyflavonoid
US3400026A (en) * 1967-01-16 1968-09-03 Du Pont Thickened aqueous inorganic oxidizer salt explosive composition containing dissolvedproteinaceous material

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN106748590A (zh) * 2016-12-21 2017-05-31 四川雅化实业集团股份有限公司 一种粘性炸药用粘合剂及其制备方法
RU2789321C2 (ru) * 2021-07-15 2023-02-01 Федеральное государственное автономное образовательное учреждение высшего образования «Дальневосточный федеральный университет» (ДВФУ) Водосодержащее взрывчатое вещество

Also Published As

Publication number Publication date
GB1225205A (enrdf_load_stackoverflow) 1971-03-17
DE1915456B2 (de) 1975-03-06
DE1915456A1 (de) 1969-11-06
DE1915456C3 (de) 1975-10-09

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