US2096009A - Method for making semi-pyrophoric iron - Google Patents
Method for making semi-pyrophoric iron Download PDFInfo
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- US2096009A US2096009A US630702A US63070232A US2096009A US 2096009 A US2096009 A US 2096009A US 630702 A US630702 A US 630702A US 63070232 A US63070232 A US 63070232A US 2096009 A US2096009 A US 2096009A
- Authority
- US
- United States
- Prior art keywords
- pyrophoric
- metals
- iron
- ignition
- semi
- 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
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- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 title description 24
- 229910052742 iron Inorganic materials 0.000 title description 12
- 238000000034 method Methods 0.000 title description 9
- 229910052751 metal Inorganic materials 0.000 description 20
- 239000002184 metal Substances 0.000 description 20
- 150000002739 metals Chemical class 0.000 description 18
- 239000000203 mixture Substances 0.000 description 15
- 238000006243 chemical reaction Methods 0.000 description 9
- 239000000126 substance Substances 0.000 description 9
- 239000007789 gas Substances 0.000 description 8
- 229910052739 hydrogen Inorganic materials 0.000 description 8
- 239000001257 hydrogen Substances 0.000 description 8
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 7
- 239000011230 binding agent Substances 0.000 description 7
- 238000002485 combustion reaction Methods 0.000 description 5
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 4
- UQSXHKLRYXJYBZ-UHFFFAOYSA-N Iron oxide Chemical compound [Fe]=O UQSXHKLRYXJYBZ-UHFFFAOYSA-N 0.000 description 4
- 238000004519 manufacturing process Methods 0.000 description 4
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 3
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 3
- 235000019506 cigar Nutrition 0.000 description 3
- 235000019504 cigarettes Nutrition 0.000 description 3
- 150000002506 iron compounds Chemical class 0.000 description 3
- 150000002736 metal compounds Chemical class 0.000 description 3
- 230000001473 noxious effect Effects 0.000 description 3
- 239000003960 organic solvent Substances 0.000 description 3
- 229910052698 phosphorus Inorganic materials 0.000 description 3
- 239000011574 phosphorus Substances 0.000 description 3
- 239000000243 solution Substances 0.000 description 3
- 239000007858 starting material Substances 0.000 description 3
- 229910052717 sulfur Inorganic materials 0.000 description 3
- 239000011593 sulfur Substances 0.000 description 3
- QAOWNCQODCNURD-UHFFFAOYSA-N sulfuric acid Substances OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 3
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- 229920002472 Starch Polymers 0.000 description 2
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 description 2
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 2
- 229910052799 carbon Inorganic materials 0.000 description 2
- 239000004927 clay Substances 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- 229940062993 ferrous oxalate Drugs 0.000 description 2
- 239000003292 glue Substances 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- 239000011261 inert gas Substances 0.000 description 2
- OWZIYWAUNZMLRT-UHFFFAOYSA-L iron(2+);oxalate Chemical compound [Fe+2].[O-]C(=O)C([O-])=O OWZIYWAUNZMLRT-UHFFFAOYSA-L 0.000 description 2
- 229910052760 oxygen Inorganic materials 0.000 description 2
- 239000001301 oxygen Substances 0.000 description 2
- 239000000843 powder Substances 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- 239000008107 starch Substances 0.000 description 2
- 235000019698 starch Nutrition 0.000 description 2
- XTEGARKTQYYJKE-UHFFFAOYSA-M Chlorate Chemical class [O-]Cl(=O)=O XTEGARKTQYYJKE-UHFFFAOYSA-M 0.000 description 1
- 229920000084 Gum arabic Polymers 0.000 description 1
- 241000978776 Senegalia senegal Species 0.000 description 1
- SMEGJBVQLJJKKX-HOTMZDKISA-N [(2R,3S,4S,5R,6R)-5-acetyloxy-3,4,6-trihydroxyoxan-2-yl]methyl acetate Chemical compound CC(=O)OC[C@@H]1[C@H]([C@@H]([C@H]([C@@H](O1)O)OC(=O)C)O)O SMEGJBVQLJJKKX-HOTMZDKISA-N 0.000 description 1
- 239000000205 acacia gum Substances 0.000 description 1
- 235000010489 acacia gum Nutrition 0.000 description 1
- 229940081735 acetylcellulose Drugs 0.000 description 1
- 238000007792 addition Methods 0.000 description 1
- 238000005275 alloying Methods 0.000 description 1
- 229940072049 amyl acetate Drugs 0.000 description 1
- PGMYKACGEOXYJE-UHFFFAOYSA-N anhydrous amyl acetate Natural products CCCCCOC(C)=O PGMYKACGEOXYJE-UHFFFAOYSA-N 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 150000004649 carbonic acid derivatives Chemical class 0.000 description 1
- 239000000969 carrier Substances 0.000 description 1
- 229920002301 cellulose acetate Polymers 0.000 description 1
- ZCDOYSPFYFSLEW-UHFFFAOYSA-N chromate(2-) Chemical class [O-][Cr]([O-])(=O)=O ZCDOYSPFYFSLEW-UHFFFAOYSA-N 0.000 description 1
- 229910017052 cobalt Inorganic materials 0.000 description 1
- 239000010941 cobalt Substances 0.000 description 1
- GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 239000002360 explosive Substances 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- MNWFXJYAOYHMED-UHFFFAOYSA-M heptanoate Chemical compound CCCCCCC([O-])=O MNWFXJYAOYHMED-UHFFFAOYSA-M 0.000 description 1
- 150000002431 hydrogen Chemical class 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- NUJOXMJBOLGQSY-UHFFFAOYSA-N manganese dioxide Inorganic materials O=[Mn]=O NUJOXMJBOLGQSY-UHFFFAOYSA-N 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 210000002418 meninge Anatomy 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 150000002823 nitrates Chemical class 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 150000003891 oxalate salts Chemical class 0.000 description 1
- 150000002978 peroxides Chemical class 0.000 description 1
- 231100000614 poison Toxicity 0.000 description 1
- 230000007096 poisonous effect Effects 0.000 description 1
- VKJKEPKFPUWCAS-UHFFFAOYSA-M potassium chlorate Chemical compound [K+].[O-]Cl(=O)=O VKJKEPKFPUWCAS-UHFFFAOYSA-M 0.000 description 1
- 239000008262 pumice Substances 0.000 description 1
- 239000010453 quartz Substances 0.000 description 1
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N silicon dioxide Inorganic materials O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 238000007711 solidification Methods 0.000 description 1
- 230000008023 solidification Effects 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 239000004575 stone Substances 0.000 description 1
- 150000003467 sulfuric acid derivatives Chemical class 0.000 description 1
- 150000003892 tartrate salts Chemical class 0.000 description 1
- 238000005979 thermal decomposition reaction Methods 0.000 description 1
- 239000011787 zinc oxide Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C21—METALLURGY OF IRON
- C21B—MANUFACTURE OF IRON OR STEEL
- C21B13/00—Making spongy iron or liquid steel, by direct processes
-
- C—CHEMISTRY; METALLURGY
- C21—METALLURGY OF IRON
- C21B—MANUFACTURE OF IRON OR STEEL
- C21B15/00—Other processes for the manufacture of iron from iron compounds
- C21B15/04—Other processes for the manufacture of iron from iron compounds from iron carbonyl
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
- Y02P10/00—Technologies related to metal processing
- Y02P10/10—Reduction of greenhouse gas [GHG] emissions
- Y02P10/134—Reduction of greenhouse gas [GHG] emissions by avoiding CO2, e.g. using hydrogen
Definitions
- the reduction 3 provides for a safety igof the metal compounds may be carried out by nition mixture which may easily be ignited on thermal decomposition in presence of inert gases the usual friction surfaces for safety matches or by treatment with hydrogen at raised temperand are combusted without flame and without atures.
- Self- A metal is semi-pyrophoric when, on the 35 ignition of the new ignition mixtures is imposone hand, it is not self-ignitable by mere consible.
- the new ignition mixtures are especially tact with air and, on the other hand, is not so suitable as igniting heads for cigars, cigarettes diiiicultly ignitable as in the normal state but can and matches, which are safely and efllciently be brought into a state of ignition by friction-on 4o lighted by mere friction on one of theusual frica friction surface.
- a metal is 40 tion surfaces for matches, which surfaces are semi-pyrophoric when its ignition temperapreferably arranged on or in the packages for t the cigars, cigarettes matches (1) Is not so low that it ignites by contact with According to the invention the phosphorus, sulfur or the like present in the known ignition Is not so high t t it does not ignite by 45 mixtures is replaced by metals with a sufficiently gig i fi gi ggf ggs fi gg fi igi ifiga (3) But is of such a nature that mere friction on combustion do not furnish volatile combustion on lfnctlon surface Sumclent lgmtmg the products but solid oxides in form of a powder.
- Pyrophoric metals may be converted into semipyrophoric metals by a shorter or longer heat treatment in presence of inert gases, such as nitrogen, hydrogen and the like or by mixing or alloying them with substance, not self-ignitable by contact with air, such as oxides.
- inert gases such as nitrogen, hydrogen and the like
- substance not self-ignitable by contact with air, such as oxides.
- the duration of the treatment is a function of the temperature. Moreover temperature and duration of the treatment are different for diiferent metals, gases and pressures employed. It is therefore not possible to give general data for temperature and duration of the-treatment, but the following examples may lead the expert in finding the conditions for making semi-pyrophoric' metals other than iron or semi-pyrophoric iron from other starting materials or by a modified method.
- Example I 10 g. of ferrous oxalate are heated to about 400 C. in streaming hydrogen, which has been dried by passing it through concentrated sulfuric acid before entering the reaction zone and which passes this zone at a moderate rate corresponding to about two gas .bubbles leaving the sulfuric acid per second.
- the amount of gases leaving the reaction zone decreases, which is the case after about one hour, the reaction is finished.
- the heating is stopped and a rapid cooling is effected by passing hydrogen through the reaction zone.
- room temperature has been reached a black powder is obtained not ignitable by contact with air, at room temperature, but ignitable, when contacting it with air at about 180 0.
- Example II 28 parts of the semi-pyrophoric iron produced in the manner described are mixed with 25 parts of potassium chlorate, 1 part of pyrolusite and 18 parts of powdered burnt clay. The mixture is powdered and mixed while stirring with80 parts of a 4% solution of collodion in volatile organic solvents, some ether and alcohol being added to the pappy mixture if necessary. The mixture is placed on the top of a cigar or cigarette in any convenient manner, thus obtaining a firmly adhering ignition head on the article after evaporation of the volatile solvent at the air.
- the igniting mixture described above may contain other substances, such as fillers and the like, or may be combined with other pyrotechnic mixtures. It may be arranged on any inflammable carrier and thus serve to light any combustible substance.
- solution of collodion employed as binding agent in the above example may be replaced by solutions of other binders, such as acetyl cellulose and the like, in volatile organic solvents,
- binders containing volatile organic solvents are preferred, as the solidification of the ignition mixtures on their carriers is accelerated, when the binder contains volatile liquids as solvent.
- the amount of binder used is kept as low as possible and preferably such binders are employed, which are easily and completely combusted without the evolution of noxious or bad smelling gases or of both.
- a method for making semi-pyrophoric iron which consists in reducing iron compounds with hydrogen at reaction conditions with respect to temperature and duration of reaction, above which pyrophoric and below which normal iron are obtained, iron oxide being used as starting material.
- a method for making semi-pyrophoric iron which consists in reducing iron compounds with hydrogen at reaction conditions with respect to temperature and duration of reaction, above which pyrophoric and below which normal iron are obtained, ferrous oxalate being used as starting material.
- a method for making semi-pyrophoric iron which consists in a reduction by means of hydrogen of iron compounds at increased temperature, keeping the conditions of reaction with respect to temperature and duration within limits, beyond which pyrophoric and normal iron respectively are obtained by the same treatment.
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- Engineering & Computer Science (AREA)
- Chemical & Material Sciences (AREA)
- Manufacturing & Machinery (AREA)
- Materials Engineering (AREA)
- Metallurgy (AREA)
- Organic Chemistry (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Solid Fuels And Fuel-Associated Substances (AREA)
- Treating Waste Gases (AREA)
Description
UNITED STATES PATENT OFFICE METHOD FOR MAKING SEMI-PYROPHORIC IRON Alfred Schmid, Basel, Switzerland, assignor to Oswald F. Wyss, Zurich, Switzerland No Drawing. Application August 27, 1932, Serial No. 630,702. In Germany August 28, 1931 3 Claims. (Cl. 75-34) This invention relates to safety ignition mix- For many purposes ordinary metals would yield tures and to their manufacture and has for its ignition mixtures, the ignition of which would main object to provide for a safety ignition mixbe too diflicult for the purpose in question. The ture, the combustion of which takes place withinvention provides for means to bring these 6 out flame and without the production of poisonmetals into a form, in which their rapid oxidaous or bad smelling gases or of both. tion or combustion is facilitated.
The known ignition mixtures used for starting It is known, that certain metals such as iron combustion processes generally consist of the or cobalt may be obtained in the pyrophoric following constituents: form by reducing at relatively low temperatures 10 (a) Easily mposable substances yie din suitable compounds of these metals with stream- 10 oxygen by decomposition, such as chlorates, niing hydrogen. These pyrophoric metals are, trates, chromates, peroxides, and the like. however, ignited and combusted by contact with (b) Substances easily inflammable at low temoxygen or air at room temperature. This pyroperatures such as phosphorus, sulfur, carbon or phoric form of metals is not suitable for the purcompounds of the same. pose of the invention and the invention there- 5 (0) Additions of hard and chemically inert forehas for its further object, toprovide for -a substances increasing friction, such as quartz, method, which enables the manufacture of metals clay, pumice stone and the like. w in such a form, that they maybe ignited with air (it) Binding agents such as "glue, starch, gum at temperatures above atmospheric temperature, arabic and the like. preferably above 50 C. but below 300 C. I-have 2 (e) Substances preventing an explosive comnamed this form of metals semi-pyrophoric, bustion such as zinc oxide, iron oxide and the which is, an intermediate form between pyrolike, phoric and normal form. This method for mak- Due to the presence of the substances mening' semi-'pyrophoric metals consists in a reductioned under I) all known ignition mixtures are tion of metalcompounds suitable for the manu- 25 combusted with flames and evolution of poisonous facture of pyrophoric' metals under such modior evil smelling gases or of both. Their use is fied reducing conditions that neither the pyrotherefore impossible in all those cases where open phoric. nor the normal form is obtained or in flames of the evolved gases are dangerous or treatment of pyrophoric metals which makes noxious. them more diflicultly ignitable. The reduction 3 The present invention provides for a safety igof the metal compounds may be carried out by nition mixture which may easily be ignited on thermal decomposition in presence of inert gases the usual friction surfaces for safety matches or by treatment with hydrogen at raised temperand are combusted without flame and without atures. I
evolution of noxious or evil smelling gases. Self- A metal is semi-pyrophoric when, on the 35 ignition of the new ignition mixtures is imposone hand, it is not self-ignitable by mere consible. The new ignition mixtures are especially tact with air and, on the other hand, is not so suitable as igniting heads for cigars, cigarettes diiiicultly ignitable as in the normal state but can and matches, which are safely and efllciently be brought into a state of ignition by friction-on 4o lighted by mere friction on one of theusual frica friction surface. Or, in other words, a metal is 40 tion surfaces for matches, which surfaces are semi-pyrophoric when its ignition temperapreferably arranged on or in the packages for t the cigars, cigarettes matches (1) Is not so low that it ignites by contact with According to the invention the phosphorus, sulfur or the like present in the known ignition Is not so high t t it does not ignite by 45 mixtures is replaced by metals with a sufficiently gig i fi gi ggf ggs fi gg fi igi ifiga (3) But is of such a nature that mere friction on combustion do not furnish volatile combustion on lfnctlon surface Sumclent lgmtmg the products but solid oxides in form of a powder. meta 50 The main feature of the new ignition mixtures is Temperature and @I these trfeatments the absence of phosphorus, sulfur, carbon or their must be kept Within 11ml, ut51de 0f Whlch P compounds, the inflammability f th mixture phoric or normal metals are obtained. Starting being solely due to the combination of oxygen materials for the method according to the invenyielding substances with easily ignitable metals. tion are inorganic or organic metal compounds 55 friction on a friction surface;
such as oxides, nitrates, carbonates, sulfates, oxalates, tartrates or the like.
Pyrophoric metals may be converted into semipyrophoric metals by a shorter or longer heat treatment in presence of inert gases, such as nitrogen, hydrogen and the like or by mixing or alloying them with substance, not self-ignitable by contact with air, such as oxides.
In both cases for the manufacture of semipyrophoric metals the duration of the treatment is a function of the temperature. Moreover temperature and duration of the treatment are different for diiferent metals, gases and pressures employed. It is therefore not possible to give general data for temperature and duration of the-treatment, but the following examples may lead the expert in finding the conditions for making semi-pyrophoric' metals other than iron or semi-pyrophoric iron from other starting materials or by a modified method.
Example I 10 g. of ferrous oxalate are heated to about 400 C. in streaming hydrogen, which has been dried by passing it through concentrated sulfuric acid before entering the reaction zone and which passes this zone at a moderate rate corresponding to about two gas .bubbles leaving the sulfuric acid per second. When the amount of gases leaving the reaction zone decreases, which is the case after about one hour, the reaction is finished. The heating is stopped and a rapid cooling is effected by passing hydrogen through the reaction zone. When room temperature has been reached a black powder is obtained not ignitable by contact with air, at room temperature, but ignitable, when contacting it with air at about 180 0.
Example II 28 parts of the semi-pyrophoric iron produced in the manner described are mixed with 25 parts of potassium chlorate, 1 part of pyrolusite and 18 parts of powdered burnt clay. The mixture is powdered and mixed while stirring with80 parts of a 4% solution of collodion in volatile organic solvents, some ether and alcohol being added to the pappy mixture if necessary. The mixture is placed on the top of a cigar or cigarette in any convenient manner, thus obtaining a firmly adhering ignition head on the article after evaporation of the volatile solvent at the air.
The igniting mixture described above may contain other substances, such as fillers and the like, or may be combined with other pyrotechnic mixtures. It may be arranged on any inflammable carrier and thus serve to light any combustible substance.
The solution of collodion employed as binding agent in the above example may be replaced by solutions of other binders, such as acetyl cellulose and the like, in volatile organic solvents,
such as alcohol, ether, acetone, amyl acetate and the like. Also aqueous solutions of glue, starch, gum arabic and the like may be employed, although binders containing volatile organic solvents are preferred, as the solidification of the ignition mixtures on their carriers is accelerated, when the binder contains volatile liquids as solvent. The amount of binder used is kept as low as possible and preferably such binders are employed, which are easily and completely combusted without the evolution of noxious or bad smelling gases or of both.
I claim:
1. A method for making semi-pyrophoric iron which consists in reducing iron compounds with hydrogen at reaction conditions with respect to temperature and duration of reaction, above which pyrophoric and below which normal iron are obtained, iron oxide being used as starting material.
2. A method for making semi-pyrophoric iron which consists in reducing iron compounds with hydrogen at reaction conditions with respect to temperature and duration of reaction, above which pyrophoric and below which normal iron are obtained, ferrous oxalate being used as starting material.
3. A method for making semi-pyrophoric iron which consists in a reduction by means of hydrogen of iron compounds at increased temperature, keeping the conditions of reaction with respect to temperature and duration within limits, beyond which pyrophoric and normal iron respectively are obtained by the same treatment.
ALFRED SCHLHD.
Priority Applications (4)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DESCH95224D DE595068C (en) | 1931-08-29 | 1931-08-29 | Safety fuse |
| US700147A US2071710A (en) | 1931-08-29 | 1933-11-28 | Ignition composition |
| US118171A US2103698A (en) | 1931-08-29 | 1936-12-29 | Safety ignition composition containing semi-pyrophoric metal |
| US158593A US2207879A (en) | 1931-08-29 | 1937-08-11 | Method of making semipyrophoric iron and the product obtained thereby |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE2096009X | 1931-08-28 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US2096009A true US2096009A (en) | 1937-10-19 |
Family
ID=7984725
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US630702A Expired - Lifetime US2096009A (en) | 1931-08-28 | 1932-08-27 | Method for making semi-pyrophoric iron |
Country Status (1)
| Country | Link |
|---|---|
| US (1) | US2096009A (en) |
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2497268A (en) * | 1944-07-26 | 1950-02-14 | Electro Chimie Metal | Permanent magnets and method for the obtention of the same |
| US2592321A (en) * | 1943-03-01 | 1952-04-08 | Electro Chimie Metal | Method for the manufacture of agglomerable iron powder |
| US2651105A (en) * | 1942-04-07 | 1953-09-08 | Electro Chimie Metal | Manufacture of permanent magnets |
-
1932
- 1932-08-27 US US630702A patent/US2096009A/en not_active Expired - Lifetime
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2651105A (en) * | 1942-04-07 | 1953-09-08 | Electro Chimie Metal | Manufacture of permanent magnets |
| US2592321A (en) * | 1943-03-01 | 1952-04-08 | Electro Chimie Metal | Method for the manufacture of agglomerable iron powder |
| US2497268A (en) * | 1944-07-26 | 1950-02-14 | Electro Chimie Metal | Permanent magnets and method for the obtention of the same |
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