US1665635A - John wesley harden - Google Patents
John wesley harden Download PDFInfo
- Publication number
- US1665635A US1665635A US1665635DA US1665635A US 1665635 A US1665635 A US 1665635A US 1665635D A US1665635D A US 1665635DA US 1665635 A US1665635 A US 1665635A
- Authority
- US
- United States
- Prior art keywords
- powder
- metal
- impurities
- uranium
- dissolved
- 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
Links
- 229910052751 metal Inorganic materials 0.000 description 72
- 239000002184 metal Substances 0.000 description 72
- 239000000843 powder Substances 0.000 description 72
- 239000012535 impurity Substances 0.000 description 40
- 229910052770 Uranium Inorganic materials 0.000 description 32
- 239000007788 liquid Substances 0.000 description 32
- JFALSRSLKYAFGM-UHFFFAOYSA-N uranium(0) Chemical compound [U] JFALSRSLKYAFGM-UHFFFAOYSA-N 0.000 description 32
- 238000005406 washing Methods 0.000 description 28
- 238000000034 method Methods 0.000 description 24
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 22
- VEXZGXHMUGYJMC-UHFFFAOYSA-N HCl Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 20
- 239000002904 solvent Substances 0.000 description 20
- 239000002253 acid Substances 0.000 description 18
- 150000002739 metals Chemical class 0.000 description 18
- IXCSERBJSXMMFS-UHFFFAOYSA-N hydrogen chloride Substances Cl.Cl IXCSERBJSXMMFS-UHFFFAOYSA-N 0.000 description 16
- 229910000041 hydrogen chloride Inorganic materials 0.000 description 16
- OKKJLVBELUTLKV-UHFFFAOYSA-N methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 16
- 239000000243 solution Substances 0.000 description 16
- 239000000463 material Substances 0.000 description 12
- FAPWRFPIFSIZLT-UHFFFAOYSA-M sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 12
- 150000001875 compounds Chemical class 0.000 description 10
- 238000000746 purification Methods 0.000 description 10
- 239000006227 byproduct Substances 0.000 description 8
- 230000001427 coherent Effects 0.000 description 8
- 239000001257 hydrogen Substances 0.000 description 8
- 229910052739 hydrogen Inorganic materials 0.000 description 8
- 239000000203 mixture Substances 0.000 description 8
- 230000003647 oxidation Effects 0.000 description 8
- 238000007254 oxidation reaction Methods 0.000 description 8
- 239000000126 substance Substances 0.000 description 8
- UXVMQQNJUSDDNG-UHFFFAOYSA-L cacl2 Chemical compound [Cl-].[Cl-].[Ca+2] UXVMQQNJUSDDNG-UHFFFAOYSA-L 0.000 description 6
- 239000001110 calcium chloride Substances 0.000 description 6
- 229910001628 calcium chloride Inorganic materials 0.000 description 6
- 238000006243 chemical reaction Methods 0.000 description 6
- UFHFLCQGNIYNRP-UHFFFAOYSA-N hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 6
- 150000004679 hydroxides Chemical class 0.000 description 6
- 239000011780 sodium chloride Substances 0.000 description 6
- 235000008733 Citrus aurantifolia Nutrition 0.000 description 4
- 229910052776 Thorium Inorganic materials 0.000 description 4
- 235000015450 Tilia cordata Nutrition 0.000 description 4
- 235000011941 Tilia x europaea Nutrition 0.000 description 4
- 239000007864 aqueous solution Substances 0.000 description 4
- 230000015572 biosynthetic process Effects 0.000 description 4
- ODINCKMPIJJUCX-UHFFFAOYSA-N calcium monoxide Chemical compound [Ca]=O ODINCKMPIJJUCX-UHFFFAOYSA-N 0.000 description 4
- 239000007795 chemical reaction product Substances 0.000 description 4
- RTZKZFJDLAIYFH-UHFFFAOYSA-N diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 4
- 238000001914 filtration Methods 0.000 description 4
- 238000005755 formation reaction Methods 0.000 description 4
- 238000010438 heat treatment Methods 0.000 description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-M hydroxyl anion Chemical compound [OH-] XLYOFNOQVPJJNP-UHFFFAOYSA-M 0.000 description 4
- 230000001939 inductive effect Effects 0.000 description 4
- 239000004571 lime Substances 0.000 description 4
- 238000004519 manufacturing process Methods 0.000 description 4
- 230000004048 modification Effects 0.000 description 4
- 238000006011 modification reaction Methods 0.000 description 4
- KEAYESYHFKHZAL-UHFFFAOYSA-N sodium Chemical compound [Na] KEAYESYHFKHZAL-UHFFFAOYSA-N 0.000 description 4
- 239000011734 sodium Substances 0.000 description 4
- 229910052708 sodium Inorganic materials 0.000 description 4
- ZSLUVFAKFWKJRC-UHFFFAOYSA-N thorium Chemical compound [Th] ZSLUVFAKFWKJRC-UHFFFAOYSA-N 0.000 description 4
- JCMLRUNDSXARRW-UHFFFAOYSA-N trioxouranium Chemical compound O=[U](=O)=O JCMLRUNDSXARRW-UHFFFAOYSA-N 0.000 description 4
- 229910000439 uranium oxide Inorganic materials 0.000 description 4
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
- 238000007792 addition Methods 0.000 description 2
- 239000000292 calcium oxide Substances 0.000 description 2
- 239000003153 chemical reaction reagent Substances 0.000 description 2
- 239000002274 desiccant Substances 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 231100001004 fissure Toxicity 0.000 description 2
- 239000007789 gas Substances 0.000 description 2
- 230000036571 hydration Effects 0.000 description 2
- 238000006703 hydration reaction Methods 0.000 description 2
- 150000002431 hydrogen Chemical class 0.000 description 2
- 238000002955 isolation Methods 0.000 description 2
- 239000012457 nonaqueous media Substances 0.000 description 2
- 239000001301 oxygen Substances 0.000 description 2
- MYMOFIZGZYHOMD-UHFFFAOYSA-N oxygen Chemical compound O=O MYMOFIZGZYHOMD-UHFFFAOYSA-N 0.000 description 2
- 229910052760 oxygen Inorganic materials 0.000 description 2
- 239000002245 particle Substances 0.000 description 2
- 239000000047 product Substances 0.000 description 2
- 238000000926 separation method Methods 0.000 description 2
- 239000001117 sulphuric acid Substances 0.000 description 2
- 235000011149 sulphuric acid Nutrition 0.000 description 2
- 239000006228 supernatant Substances 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- QCWXUUIWCKQGHC-UHFFFAOYSA-N zirconium Chemical compound [Zr] QCWXUUIWCKQGHC-UHFFFAOYSA-N 0.000 description 2
- 229910052726 zirconium Inorganic materials 0.000 description 2
Classifications
-
- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22B—PRODUCTION AND REFINING OF METALS; PRETREATMENT OF RAW MATERIALS
- C22B60/00—Obtaining metals of atomic number 87 or higher, i.e. radioactive metals
- C22B60/02—Obtaining thorium, uranium, or other actinides
- C22B60/0204—Obtaining thorium, uranium, or other actinides obtaining uranium
- C22B60/0286—Obtaining thorium, uranium, or other actinides obtaining uranium refining, melting, remelting, working up uranium
-
- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22B—PRODUCTION AND REFINING OF METALS; PRETREATMENT OF RAW MATERIALS
- C22B60/00—Obtaining metals of atomic number 87 or higher, i.e. radioactive metals
- C22B60/02—Obtaining thorium, uranium, or other actinides
- C22B60/0291—Obtaining thorium, uranium, or other actinides obtaining thorium
Description
Patented Apr. 10, 1928.
UNITED STATES 1,665,635 PATENT OFFICE.
JOHN WESLEY IARDEN, OF EAST ORANGE, NEW JERSEY, ASSIGNOR TO. WESTING- HOUSE LAMP COMPANY, A CORPORATION OF PENNSYLVANIA.
PURIFICATION OI METAL POWDERS.
No Drawing.
This invention relates to a method for purifying materials with a new type of solvent and more particularly it relates to a method for the purification of metals which 6 are obtained in the powdered state by reduction and separation and are contaminated by impurities during these processes.
An object of this invention is the provision of a new type of solvent. 10 Another object of this invention is the provision of a method whereby metal powders may be obtained in a high state of purity.
A further object of the invention is the 16 provision of a method whereby metallic powders may be produced free from metallic hydroxides, oxides or other impurities.
A special object of the invention is the provision of a method whereby uranium may 20 be obtained in a state of purity sufiicient to allow its working into a coherent mass.
Other objects will be apparent from a further reading of the specification.
It is known that there are many processes practiced for obtaining metals from their compounds by which the metals are obtained in a powdered condition contaminated with certain impurities such as the by-products of the reaction and with hydroxides and a0 oxides resulting from the process which is practiced to isolate the metallic powder from its by-products and resulting also from exposure to the atmosphere. The formation of hydroxides and, subsequently, of oxides is partly due to the fact that the isolation process, usually known as washing, is done with an aqueous solution, whereby at least part of the metal powder is converted into hydroxide, which, upon heating, is converted into an oxide. The formation of these impurities is due to the fact that particles of metal powder have such large surface areas in proportion to their volume that they are very active chemically and therefore combine readily with impurities such, for example, as oxygen and hydrogen or combinations of the same.
By following the process outlined in this invention, metals prepared by a process which yields a metallic powder in an impure condition may be obtained in a high state of purity. It is therefore apparent that the present invention is very valuable when isolating easily-oxidizable metals such, for ex- ,3 ample, as uranium, thorium and zirconium,
Application filed August 21, 1922. Serial No. 583,376.
from the by-products of the reaction which effects their reduction. It has been found that this invention, as hereinafter described, is especially valuable and even necessary when it is desired to work easily-oxidizable metals from the powdered condition into a coherent mass.
According to my invention, metals may be obtained in a pure state and may be prevented from accumulating impurities by washing the reaction products with a solution comprising a non-aqueous liquid in which is dissolved a non-aqueous or anhydrous solvent of the impurities or by-products which-contaminate the metal desired. Preferably, the non-aqueous liquid is an alcohol and the solvent is. an acld and, more particularly, the alcohol may be methyl alcohol and the acid may be hydrogen chloride, although, in general, the non-aqueous liquid may be any liquid in which may be dissolved an anhydrous solvent which is necessary to dissolve the impurities which are admixed or combined with the metal desired. It will be appreciated that'the use of a nonnqueous medium will avoid the hydration or oxidation of the metal being purified when carrying out the process of isolating the metal from the impurities admixed or combined with it.
Inasmuch as the present invention is particularly'useful for the production of easil oxidizable metals in a state of purity, I w1ll illustrate the procedure employed in washing uranium, which is metal of the character mentioned.
In the reduction of uranium oxide by means of calcium chloride and sodium, :1! performed by heating these compounds in I. closed bomb, the resultant products are largely uranium metal in powdered form, sodium chloride and lime. When the sodium chloride and the lime are washed out with water and dilute acid, which has been the usual practice, a. brownish-black prodnot results, the color indicating the presence of a considerable percentage of uranium oxide. This oxide, when agglomerated,'will not conduct the electric current and, therefore, will not give satisfactory results if an 106 attempt is made to sinter or fuse the same by high-frequency induction currents in a vacuum furnace, which has been found to be the preferred method for changing this metal from the powdered or agglomerated 110 state into" a coherent mass. By practicing the present process, however, the oxide may be prevented or removed so that the metal powder, when agglomerated, may be sintered or fused by induction currents and, furthermore, contains very little hydroxide and occluded. gases so that no trouble is experienced in eliminatin these impurities when the pressed body 0 powder is treated in a vacuum furnace for the purpose of producing a coherent mass.
The procedure of washing the uranium powder, after the latter has been reduced.
from its oxide in a heated bomb or other closed container by means of calcium chloride and sodium,,may be effected by washing the reaction productswith a dilute acid suitable for the solution of calcium oxide, sodium chloride and other impurities without substantial action on the uranium as metal, subsequently decanting the supernatant liquid after the undissolved material has settled and finally filtering the undesired material. During the filtration process, the material on the filter, which is largely metallic uranium, should be kept covered with alcohol, thoroughly washed with the same and may be finally washed with ether.
This step in the process, however, which employs an aqueous solution in which is dissolved a solvent material, is not a necessary step in the purification of the powder, as my process, as hereinafter described, is suflicient in itself to free the metal from impurities" In other words, the reaction products resulting from the reduction of metal in the bomb may be completely purified by means of a non-aqueous liquid in which is dissolved an anhydrous'solvent for the impurities which are to be separated from the metal desired.
In order to further purify the uraniumaccording to my invention, the metal may be washed with a solution of dry hydrogen chloride in practically anhydrous alcohol.
- This solution may be made by slowly dropping concentrated hydrochloric acid into concentrated sulphuric acid, passing the hydrogen chloride thus liberated through drying agents such, for example, as calcium chloride, and subsequently passing the dried hydrogen chloride into practically anhydrous, say 99%, alcohol. In effecting the washing process with the solution thus made, the uranium powder may first be placed in a shallow dish and covered with practically pure methyl alcohol, 99% purity being sufficient for this purpose. A solution of hydrogen chloride in alcohol may then be added gradually and the mixture thoroughly agitated. The addition of the acid-alcohol mixture maybe continued until a small amount of hydrogen is evolved. The evolu-- tion of the hydrogen as bubbles arising from may be scraped or brushed from the filter into a closed container. In introducing uramum mto such a container, which may be a mold, care must be exercised to have 1t still 'moist with alcohol so as to protect it from oxidation but dry enough so that, when subsequently exposed to pressure in the mold, the metal may not be forced'out through the fissure formed by the junction of the two elements of the mold which will now be described.
The mold may be a closed mold consisting of two members having, for example, semicylindrical grooves cut inone face of each of the members, these members being so dis posed in relation to each other that the two semi-cylindrical grooves form a'cylindrical hole, the two members being bolted together and having the ends of the cylindrical hole closed by two plungers, at least one of which extends from one end of the mold, after the uranium powder has been placed in the hole thereof. The latter may then be placed in While I have described in detail a process for preparing one metal, modifications may be necessary for the proper reparation of other metals but these modifications, such, for example, as the concentration of the acid used, the duration oftime necessary for the purification of the powder, etc. may be readily devised by one skilled in the art.
It should be understood that my invention embraces not only the method for the purification of metal powders but of other materials and it also includes the discovery of a new solvent which comprises a 'nonaqueous liquid containing adissolved'substance, the combination being regarded as a new kind of solution or reagent for solvent purposes. It will, of course, be understood a the impurities in sai that a plurality of non-aqueous solutions may be combined in which one or more substances may be dissolved, all of which,taken together, may find valuable uses in the chemical art. Furthermore, it should be understood that the non-aqueous liquid itself, as well as the dissolved substance, may be a solvent and may be used as such.
What is claimed is:
1. The method of purifying a readily oxidizable metallic powder such as thorium, uranium, etc. which comprises treating said powder with a non-aqueous liquid which does not react with the oxides of said powder and which is capable of preventing further oxidation of said powders, and combining with said liquid an acid which will interact with the impurities with which said powder is contaminated to form compounds which are readily soluble in said liquid.
2. The method of purifying a rare metal powder which consists in protecting said powder from oxidation by a non-aqueous liquid which is incapable of reacting with said powder 01' any impurity therein, said liquid having dissolved therein, an acid which is capable of reacting with said impurities and which will not appreciably react with said metal powders to form compounds which are soluble in said liquid.
3. The method t purifying a rare metal powder such as uranium which consists in washing the same with alcohol in which is dissolved an acid capable of reacting with powder to form compounds which are soluble in said alcohol.
4.- The method of purifying a rare metal powder which consists in washing the same with alcohol in which hydrogen chloride is dissolved.
5. The method of purifying rare metal powders, which comprises washing the same with methyl alcohol in which hydrogen chloride is dissolved.
6. The method of purifying uranium powder which consists in washing it with a non-aqueous liquid in which is dissolved a solventfor the impurities with which said metal powder is contaminated.
7. The method of purifying uranium powder which consists in washing it with a nonaqueous liquid in which is dissolved an acid for the solution of the impurities which contaminate said metal powder.
. 8. The method of purifying uranium powder which consists in washing it with alcohol in which is dissolved an acid by means of which the impurities in said metal powder may be dissolved.
9. The method of purifying uranium powder which consists in washing it with an al- (3931101 in which is dissolved hydrogen chlorx 0.
10. The method of purifying uranium powder which consists in washing it with methyl alcohol in which is dissolved hydrogen chloride.
In testimony whereof, I have hereunto subscribed my name this l9thday of August,
JOHN WESLEY MARDEN.
Publications (1)
Publication Number | Publication Date |
---|---|
US1665635A true US1665635A (en) | 1928-04-10 |
Family
ID=3414898
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US1665635D Expired - Lifetime US1665635A (en) | John wesley harden |
Country Status (1)
Country | Link |
---|---|
US (1) | US1665635A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3017264A (en) * | 1959-07-28 | 1962-01-16 | Karlowicz Peter | Process for desensitizing zirconium for use in primers |
-
0
- US US1665635D patent/US1665635A/en not_active Expired - Lifetime
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3017264A (en) * | 1959-07-28 | 1962-01-16 | Karlowicz Peter | Process for desensitizing zirconium for use in primers |
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