US3512959A - Method of preparing melts of zinc base alloys and improved flux therefor - Google Patents
Method of preparing melts of zinc base alloys and improved flux therefor Download PDFInfo
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- US3512959A US3512959A US3512959DA US3512959A US 3512959 A US3512959 A US 3512959A US 3512959D A US3512959D A US 3512959DA US 3512959 A US3512959 A US 3512959A
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- 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
- C22B9/00—General processes of refining or remelting of metals; Apparatus for electroslag or arc remelting of metals
- C22B9/10—General processes of refining or remelting of metals; Apparatus for electroslag or arc remelting of metals with refining or fluxing agents; Use of materials therefor, e.g. slagging or scorifying agents
-
- 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
- C22B19/00—Obtaining zinc or zinc oxide
- C22B19/30—Obtaining zinc or zinc oxide from metallic residues or scraps
-
- C—CHEMISTRY; METALLURGY
- C23—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
- C23C—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
- C23C2/00—Hot-dipping or immersion processes for applying the coating material in the molten state without affecting the shape; Apparatus therefor
- C23C2/30—Fluxes or coverings on molten baths
-
- 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
- Y02P10/20—Recycling
Definitions
- the improved flux preferably contains a small amount, up to 20 or 25%, of the total of said chlorides of an inorganic fluoride selected from sodium and potassium cryolites and silicofluorides and mixtures of one or more thereof.
- the present invention relates'to a method of fluxing
- the metal is heated to a temperature of 780 F. or above, usually at 850 to 1000 F.
- parts of the melted metal within the dross on the bath surface are often prevented from coalescing with other parts 'because of the presence of oxides. The result is that a considerable amount of metal is trapped in the dross layer over the molten metal.
- This dross layer is made up primarily of uncoalesced molten particles of the alloy, zinc oxide and an iron-aluminum compound.
- the fluxes used heretofore and considered to be most eflicient contained large amounts of zinc chloride and ammonium chloride both in mechanical and chemical combination.
- the zinc chloride-ammonium chloride fluxes cause a strong exothermic reaction in the dross. layer and have been considered to do an excellent job of releasing entrapped metal in the dross layer. They produce a desirable dry, powdery dross.
- the strong exothermic reaction is, however, not desirable for it raises the temperature of the melt above that desired and makes melt temperature hard to control.
- Both the zinc chloride and the ammonium chloride cause a large amount of smoke (visible and highly objectionable vapors) to be evolved.
- Zinc die casting alloys contain .02% to .08% of magnesium to increase tolerance of lead, cadmium and tin impurities, and about 4% of aluminum to yield eutectic type alloys.
- the reactions occurring when fluxes containing zinc chloride-ammonium chloride are used cause a loss of magnesium from the alloy.
- a decrease of the magnesium content results in the inter granular corrosion of the castings made of such alloy.
- To compensate for such loss it has been a practice to add some magnesium chloride to the flux.
- Such skimmings being the dross layer which has been removed from the surface of a zinc alloy bath. These skimmings are treated separately with fluxes.
- the magnesium chloride (MgCl considered'asanhydrous, should constitute at least 20% by Weight of the 1 total of the magnesium, sodium and potassium chlorides.
- the dross becomes wet and is hard to manage.
- the amount of magnesium chloride is less than 20%, the melting point of the flux becomes inordinately high.
- the preferred amount of magnesium chloride is 25% to 60% of the total of the magnesium, sodium and potassium chlorides in the flux. The optimum amount depends to some extent on the melting temperature or operational temperature of the melting unit.
- Operational fluxes include, therefore, those mixtures of magnesium chloride with potassium and/or with sodium chloride which melt at or below the operating temperature of the zinc alloy bath, which is usually from about 780 to 1050 F.
- the sodium chloride should constitute about to about 40% of the weight of the total of alkali chlorides and MgCl present, and about 20% to about 40% is preferred.
- the potassium chloride should be present in a maximum amount of 60% of the weight of the MgCl plus total alkali chlorides present. When at least 40% of these chlorides is made up of sodium, then the potassium chloride may be omitted and still a usable flux obtained, provided the operating temperature of the zinc alloy bath is above the melting point of the flux. Both sodium and potassium chlorides are preferably present, however, and the potassium chloride preferably should be present in amounts of about 19% to about 40% of the total of MgCl and alkali metal chlorides present.
- the magnesium chloride used need not be anhydrous if care in use of our new flux is practiced.
- the above percentages are, however, based on anhydrous MgCl Hydrated magnesium chloride (MgCl '6H O) is considerably less expensive to use than the anhydrous based on magnesium chloride content.
- MgCl '6H O MgCl Hydrated magnesium chloride
- the flux must be added gradually to the surface of the alloy bath to permit gradual vaporization of the water. One cannot plunge the flux into a molten bath. If such a procedure is used anhydrous MgCl should be used.
- We have found that the effectiveness of our new flux is increased greatly when it is stirred or worked in the dross on the surface of the molten metal.
- EXAMPLE 2 1,000 pounds of a zinc die casting alloy containing about 0.05% of magnesium and 4% of aluminum is placed in a ferrous melting pot of a melting furnace along with 1.8 to 2 pounds of the flux of Example 1. The alloy is heated to 850 F. The flux is worked or stirred into the dross on the surface of the molten metal to increase the effectiveness. No noticeable fumes or smoke is evolved and the dross becomes powdery. Upon removal from the furnace and subsequent stirring the metallic content thereof was found to be less than 0.5% of the weight thereof, and the magnesium and aluminum content of the melt remain unchanged.
- Example 3 To the ingredients of Example 1 is added 10% (by weight of the original mixture) of Na SiF The resultant flux is somewhat superior to that of Example 1 when used in Example 2. The coalescence of the metal is faster.
- EXAMPLE 4 The flux of Example 3 is applied on the surface of a suitable zinc alloy melt, as described in Example 2.. The alloy is heated to a temperature of between 780 and 1,050 F. No visible fumes are evolved from the flux and the magnesium and aluminum content of the metal remain stable.
- Example 7 The procedure of Example 6 was repeated except that Flux C of Example 5 was substituted for Flux B. The fre metal alloy recovered was 92.8% of the weight of the skimming.
- the new fluxes are generally used in amounts of about .15 to .25 of the weight of the zinc base alloys melted, although as little as .05% is effective andup to 1.0% or more may'be required.
- tluxes in amounts of 1 to 5%, based on the weight of the skimniings, are usually used, although as little as 5% gives considerable recovery, and even or more may be used.
- About 2 to 4% is optimum from an economic standpoint.
- the temperature may vary from 780 F. to 1200 F. Usually the heating is in the presence of molten metal and about 780 F. to 1050 F. is then preferred, although higher temperatures. even 1200 1 1, may he used.
- a process of recovering usable metal from the skimmings resulting from melting zinc base alloys which comprises heating the said skimmings in intimate contact with a mixture of MgCl and at least one of the group consisting of NaCl and KCl, said MgCl being present in amounts of to 60 percent by weight and said group members being present in a total of at least 40 percent by weight, 0 to 40 percent of NaCl, and 0 to 60 percent of KCl being present, said heating being at a temperature at least equal to the melting. point of said mixture.
- a flux comprising a mixture of MgCl and at least one of r the group consisting of NaCl and KCI, said MgCl being present in amounts of 20 to 60 percent by weight and said group members being present in a total of at least 40 percent by weight, 0 to 40 percent of NaCl, and 0 to 60 percent of KCl being present to the surface of the bath; stirring the flux on said surface and stirring the resulting,
- powdery dross to agglomerate spheroids of molten metal and return them to the metal bath. 7. The process of claim 6 wherein the powdery dross is removed from the metallic bath and subsequently stirred to effect agglomerationof the metal spheroids contained therein.
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- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Mechanical Engineering (AREA)
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- Organic Chemistry (AREA)
- Manufacturing & Machinery (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Manufacture And Refinement Of Metals (AREA)
Description
United: States Patent 3,512,959 METHOD OF PREPARING MELTS OFZINC BASE- ALLOYS AND IMPROVED FLUX THEREFOR William F. Joseph, Rocky River, and John F. Wallace, Cleveland, Ohio, assignors to Rossborough Supply Company, Cleveland, Ohio, a corporation of Ohio No Drawing. Filed Sept. 27, 1967, Ser. No. 671,114 Int. Cl. CZZb 19/30, 19/32 U.S. Cl. 75-87 7 Claims ABSTRACT OF THE DISCLOSURE More eflicient recovery of usable metal is obtained without objectionable smoke and fumes, iron pick up or loss of magnesium from the. alloy by adding to the dross layer on the surface of a zinc base alloy bath a flux com: prising essentially 20 to 60 percent by weight of magnesium chloride (calculated as anhydrous) and at least 40 percent by weight total of sodium and potassium chlorides, the temperature to which the flux is heated being above the melting point of the flux. The sodium chloride may be present in amounts of 0 to 45 percent by weight and the potassium chloride may be present in amounts of 0 to 60 percent by weight although. a superior [flux results when sodium and potassium chlorides are each present in amounts of 20 to 40 percent of the total. When the zinc alloy contains aluminum, the improved flux preferably contains a small amount, up to 20 or 25%, of the total of said chlorides of an inorganic fluoride selected from sodium and potassium cryolites and silicofluorides and mixtures of one or more thereof.
The present invention relates'to a method of fluxing,
melting and maintaining zinc alloys in a form suitable for die casting or other melting of zinc and to an improved flux therefor. In the melting of zinc base alloys for die casting or other purposes, the metal is heated to a temperature of 780 F. or above, usually at 850 to 1000 F. During the melting operation, parts of the melted metal Within the dross on the bath surface are often prevented from coalescing with other parts 'because of the presence of oxides. The result is that a considerable amount of metal is trapped in the dross layer over the molten metal. This dross layer is made up primarily of uncoalesced molten particles of the alloy, zinc oxide and an iron-aluminum compound.
In order to facilitate coalescing of major portions of the molten metal so that it is returned to the melt, it is customary to add to the dross layer on the surface of the metal during initial and subsequent meltings, substantial quantities of a flux. The fluxes used heretofore have facilitated coalescence of a major portion or most of the molten metal particles in the dross layer so that the metal is returned to the bath.
The fluxes used heretofore and considered to be most eflicient contained large amounts of zinc chloride and ammonium chloride both in mechanical and chemical combination. The zinc chloride-ammonium chloride fluxes cause a strong exothermic reaction in the dross. layer and have been considered to do an excellent job of releasing entrapped metal in the dross layer. They produce a desirable dry, powdery dross. The strong exothermic reaction is, however, not desirable for it raises the temperature of the melt above that desired and makes melt temperature hard to control. Both the zinc chloride and the ammonium chloride cause a large amount of smoke (visible and highly objectionable vapors) to be evolved. These vapors are toxic, tend to cause illness, and constitute a health hazard. Authorities concerned with air pollu- Patented May 19, 1970 tion have objected to the discharge of such smoke into the atmosphere. Compliance with the smoke abatement requirements necessitates the installation and operation of exepensive equipment by companies using the prior fluxes.
Zinc die casting alloys contain .02% to .08% of magnesium to increase tolerance of lead, cadmium and tin impurities, and about 4% of aluminum to yield eutectic type alloys. The reactions occurring when fluxes containing zinc chloride-ammonium chloride are used cause a loss of magnesium from the alloy. A decrease of the magnesium content results in the inter granular corrosion of the castings made of such alloy. To compensate for such loss it has been a practice to add some magnesium chloride to the flux.
It is a prime object of the present invention to provide a flux which permits melting of zinc alloys without obnoxious smoke or highly toxic fumes.
It is another object of the present invention to provide fluxes for zinc alloys which produce a finely powdered dross with a higher recovery of metal from such dross than has been obtainable with the prior art.
It is still another object of the invention to provide more efficient fluxes for zinc 'base alloy baths that produce a powdery dross, increase the recovery of metal therefrom, produce no appreciable exothermic reaction when used, do not cause detrimental consumption or loss of magnesium from the zinc alloy bath, and reduce aluminum loss from the alloy because of the absence of said exothermic reaction.
It is still another object. of this invention to provide a method of treating zinc base alloys during the melting, alloying or casting thereof, which method increases the proportion of usable metal over that before obtainable, provides a dross that is powdery and easily removed from the metal and does not cause objectionable smoke.
It is another object of the present invention to provide a method of recovering more efiiciently usable metal from the skimming of zinc base alloy baths. Such skimmings being the dross layer which has been removed from the surface of a zinc alloy bath. These skimmings are treated separately with fluxes.
We have found in accordance with the present invention that the above and other objects are obtained by treating the dross upon zinc base alloy baths, with a flux comprising essentially magnesium chloride and at least one chloride selected from sodium and potassium chlorides. Our new flux is preferably obtained by mixing certain proportions of magnesium chloride with both sodium chloride and potassium chloride and, preferably, in cases where aluminum is in the alloy, some inorganic ternary fluoride compound selected from one or more of cryolite (Na AlF potassium cryolite (K AlF sodium silicofluoride (Na SiF and potassium silicofluoride (K SiF The silicofluorides and cryolites can provide a mild exothermic reaction when the flux is added to the surface of a zinc alloy bath.
Our new flux should have little if any ,zinc chloride and ammonium chloride as even a comparatively small amount of these causes smoking. However, up to 5% or so of each of these materials based on the total weight of MgCl KCl and NaCl present can be tolerated in many applications.
The magnesium chloride (MgCl considered'asanhydrous, should constitute at least 20% by Weight of the 1 total of the magnesium, sodium and potassium chlorides.
When more than 60% of MgCl is present, the dross becomes wet and is hard to manage. When the amount of magnesium chloride is less than 20%, the melting point of the flux becomes inordinately high. The preferred amount of magnesium chloride is 25% to 60% of the total of the magnesium, sodium and potassium chlorides in the flux. The optimum amount depends to some extent on the melting temperature or operational temperature of the melting unit.
The exact function of the sodium and potassium chlorides is not fully understood, but they cooperate with the magnesium in some manner to produce the unique properties in the flux. When the total of these two materials is less than 40% of the total of the MgCl and alkali metal chlorides the dross becomes wet.
We have found that to be elfective the flux must melt at or below the operating temperature of the zinc alloy bath. Operational fluxes include, therefore, those mixtures of magnesium chloride with potassium and/or with sodium chloride which melt at or below the operating temperature of the zinc alloy bath, which is usually from about 780 to 1050 F.
The sodium chloride should constitute about to about 40% of the weight of the total of alkali chlorides and MgCl present, and about 20% to about 40% is preferred.
The potassium chloride should be present in a maximum amount of 60% of the weight of the MgCl plus total alkali chlorides present. When at least 40% of these chlorides is made up of sodium, then the potassium chloride may be omitted and still a usable flux obtained, provided the operating temperature of the zinc alloy bath is above the melting point of the flux. Both sodium and potassium chlorides are preferably present, however, and the potassium chloride preferably should be present in amounts of about 19% to about 40% of the total of MgCl and alkali metal chlorides present.
Our new fluxes when applied to the surface of a zinc alloy bath are not even mildly exothermic unless the aforesaid fluorides are present. The application of our fluxes to the surface of a zinc alloy bath serves to release a substantial portion of the free metallic zinc particles entrapped in the surface covering or dross. Subsequently the dross remaining becomes dry and powdery and is easily removed from the surface of the bath. It has been found that these skimmings have high heat insulating characteristics such that the remaining spheroids of molten Zinc which were not released when the flux was applied to the surface of the bath can be agglomerated and salvaged apart from the melting bath. By simple stirring of the skimmings, this free metal accumulates to such an extent that the metallic content thereof is de creased to about 0.5%, or even less. This compares with 0.8% for the best obtainable practice heretofore followed and with the 2% to 3% resulting in the use of ordinary practices. We have found no loss of aluminum and no pick up of iron in melts prepared and maintained when using our new fluxes.
The magnesium chloride used need not be anhydrous if care in use of our new flux is practiced. The above percentages are, however, based on anhydrous MgCl Hydrated magnesium chloride (MgCl '6H O) is considerably less expensive to use than the anhydrous based on magnesium chloride content. When hydrated magnesium chloride is used the flux must be added gradually to the surface of the alloy bath to permit gradual vaporization of the water. One cannot plunge the flux into a molten bath. If such a procedure is used anhydrous MgCl should be used. We have found that the effectiveness of our new flux is increased greatly when it is stirred or worked in the dross on the surface of the molten metal.
The following examples, in which percentages are by weight, illustrate the invention.
EXAMPLE 1 Percent MgCl '6H O NaCl 27.3 KCl 27.4 K A1Fs or Na3AlF 3.0
The above ingredients are thoroughly mixed and packaged in a closed container.
EXAMPLE 2 1,000 pounds of a zinc die casting alloy containing about 0.05% of magnesium and 4% of aluminum is placed in a ferrous melting pot of a melting furnace along with 1.8 to 2 pounds of the flux of Example 1. The alloy is heated to 850 F. The flux is worked or stirred into the dross on the surface of the molten metal to increase the effectiveness. No noticeable fumes or smoke is evolved and the dross becomes powdery. Upon removal from the furnace and subsequent stirring the metallic content thereof was found to be less than 0.5% of the weight thereof, and the magnesium and aluminum content of the melt remain unchanged.
EXAMPLE 3 To the ingredients of Example 1 is added 10% (by weight of the original mixture) of Na SiF The resultant flux is somewhat superior to that of Example 1 when used in Example 2. The coalescence of the metal is faster.
EXAMPLE 4 The flux of Example 3 is applied on the surface of a suitable zinc alloy melt, as described in Example 2.. The alloy is heated to a temperature of between 780 and 1,050 F. No visible fumes are evolved from the flux and the magnesium and aluminum content of the metal remain stable.
EXAMPLE 5 Three separate fluxes based on MgCl -6H O were prepared by mixing together the ingredients shown in the following table:
Flux (percent) A B o 42 38 3s 2s 26 26 2s 25 25 2 1 1 0 10 0 0 0 10 EXAMPLE 6 1,000 grams of skimmings, resulting from melting and skimming the dross from zinc die cast gates and sprues were melted in a graphite pot at 1000 F. To these molten skimmings were added 30 grams of Flux B above by slowly mixing the flux into the skimmings. A powdery dross was obtained and 935 grams of free metal alloy were recovered from the skimmings, representing a yield of 93.5%.
EXAMPLE 7 The procedure of Example 6 Was repeated except that Flux C of Example 5 was substituted for Flux B. The fre metal alloy recovered was 92.8% of the weight of the skimming.
EXAMPLE 8 The procedure of Example 6 was repeated except that Flux A of Example 5 was substituted for Flux B. 910 grams of free metal was recovered from the skimmings.
EXAMPLE 9 To 150 pounds of skimmings from a melt of zinc die cast scrap was added 4 pounds of Flux A of Example 5. The mixture was also heated to 1000 F. in a graphite pot while stirring and working the flux into the molten skimmings. 135 pounds of free metal alloy were recov-: ered for a yield of based on the weight of the skimmmg.
In making melts the new fluxes are generally used in amounts of about .15 to .25 of the weight of the zinc base alloys melted, although as little as .05% is effective andup to 1.0% or more may'be required. In recovering metal from the skimmings front zinc base alloys, tluxes in amounts of 1 to 5%, based on the weight of the skimniings, are usually used, although as little as 5% gives considerable recovery, and even or more may be used. About 2 to 4% is optimum from an economic standpoint.
When the flux is mixed slowly or stirred into theskimmings, heat sufficient to melt the flux must be used and the temperature may vary from 780 F. to 1200 F. Usually the heating is in the presence of molten metal and about 780 F. to 1050 F. is then preferred, although higher temperatures. even 1200 1 1, may he used.
It is to he understood that in accordanccwith the provisions of the patent laws, various modifications can he made in the method, procedures, compositions and products of the present invention without departing from the spirit of the same.
We claim:
1. A process of recovering usable metal from the skimmings resulting from melting zinc base alloys which comprises heating the said skimmings in intimate contact with a mixture of MgCl and at least one of the group consisting of NaCl and KCl, said MgCl being present in amounts of to 60 percent by weight and said group members being present in a total of at least 40 percent by weight, 0 to 40 percent of NaCl, and 0 to 60 percent of KCl being present, said heating being at a temperature at least equal to the melting. point of said mixture.
2. The process according to claim 1 wherein both NaCl and KO are presentin said mixture in amounts of 20 to 40 percent by weight I Y 3. The process according to claim 2 wherein 1 to (based on weight of said mixture) of an inorganic fluoride compound; selected from the group consisting of sodium and potassium 'cryolites, sodium and potassium silicofluorides and mixtures thereof, is also present in admixture with said mixture of MgC1 KCl and NaCl.
4. The process of claim 1 wherein said mixture is free from more than 5% by weight each of zinc and ammonium chlorides.
5. In a process of treating melts of a zinc base alloy wherein the metal is heated to a temperature of between 780 and 1050 F., the steps which comprise applying a flux comprising 20 to 60% by weight of magnesium chloride (calculated as anhydrous) and at least total of sodium and potassium chlorides, the sodium chloride being present in amounts of 0 to 40% and the potassium chloride'being present in amounts of 0 to any zinc chloride and ammonium chloride present being each less than 5% of the total of said magnesium, sodium and potassium chlorides to the surface of the molten metal, stirring the flux on the said surface and stirring the resultant powdery dross to agglomerate spheroids of molten metal and return them to the metal bath.
6. In a process of treating vmelts of a zinc base alloy wherein the metal is heated to a temperature of between 780" and 1050" the steps which comprise applying a flux comprising a mixture of MgCl and at least one of r the group consisting of NaCl and KCI, said MgCl being present in amounts of 20 to 60 percent by weight and said group members being present in a total of at least 40 percent by weight, 0 to 40 percent of NaCl, and 0 to 60 percent of KCl being present to the surface of the bath; stirring the flux on said surface and stirring the resulting,
powdery dross to agglomerate spheroids of molten metal and return them to the metal bath. 7. The process of claim 6 wherein the powdery dross is removed from the metallic bath and subsequently stirred to effect agglomerationof the metal spheroids contained therein.
References Cited UNITED STATES PATENTS HENRY'W. TARRING 11, Primary Examiner US. Cl. X.R. -65, 93, 94
Applications Claiming Priority (1)
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US67111467A | 1967-09-27 | 1967-09-27 |
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US3512959A true US3512959A (en) | 1970-05-19 |
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US3512959D Expired - Lifetime US3512959A (en) | 1967-09-27 | 1967-09-27 | Method of preparing melts of zinc base alloys and improved flux therefor |
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Cited By (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4224086A (en) * | 1979-05-17 | 1980-09-23 | Aluminum Company Of America | Dip brazing flux |
US5258055A (en) * | 1992-08-31 | 1993-11-02 | International Mill Service, Inc. | Process and system for recovering zinc and other metal vapors from a gaseous stream |
EP1306452A2 (en) * | 2001-10-24 | 2003-05-02 | Kabushiki Kaisha Kobe Seiko Sho | Method for making metal oxide agglomerates |
CN102115861A (en) * | 2011-03-25 | 2011-07-06 | 东北大学 | Hot dipping covering agent |
JP2013133479A (en) * | 2011-12-26 | 2013-07-08 | Jfe Steel Corp | Method of recovering metallic zinc present in top dross of zinc-based molten metal |
WO2015016086A1 (en) * | 2013-07-30 | 2015-02-05 | 国立大学法人東北大学 | Method for recovering zinc from electric-furnace steelmaking dust and device for recovering zinc from electric-furnace steelmaking dust |
IT201900018917A1 (en) * | 2019-10-15 | 2021-04-15 | Soprin S R L | SINGLE-DOSE CAPSULE FOR GALVANIZING BATHS |
CN113122791A (en) * | 2021-04-12 | 2021-07-16 | 中山市华锌工材料科技有限公司 | Metal powder block and preparation method thereof and preparation method of hot-dip galvanizing alloy bath |
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- 1967-09-27 US US3512959D patent/US3512959A/en not_active Expired - Lifetime
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US1377374A (en) * | 1918-07-24 | 1921-05-10 | Dow Chemical Co | Manganese-magnesium alloy and method of making same |
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Cited By (14)
Publication number | Priority date | Publication date | Assignee | Title |
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US4224086A (en) * | 1979-05-17 | 1980-09-23 | Aluminum Company Of America | Dip brazing flux |
US5258055A (en) * | 1992-08-31 | 1993-11-02 | International Mill Service, Inc. | Process and system for recovering zinc and other metal vapors from a gaseous stream |
EP1306452A2 (en) * | 2001-10-24 | 2003-05-02 | Kabushiki Kaisha Kobe Seiko Sho | Method for making metal oxide agglomerates |
EP1306452A3 (en) * | 2001-10-24 | 2003-06-18 | Kabushiki Kaisha Kobe Seiko Sho | Method for making metal oxide agglomerates |
US20040216280A1 (en) * | 2001-10-24 | 2004-11-04 | Kabushiki Kaisha Kobe Seiko Sho (Kobe Steel, Ltd.) | Method for making metal oxide agglomerates |
CN102115861B (en) * | 2011-03-25 | 2012-08-29 | 东北大学 | Hot dipping covering agent |
CN102115861A (en) * | 2011-03-25 | 2011-07-06 | 东北大学 | Hot dipping covering agent |
JP2013133479A (en) * | 2011-12-26 | 2013-07-08 | Jfe Steel Corp | Method of recovering metallic zinc present in top dross of zinc-based molten metal |
WO2015016086A1 (en) * | 2013-07-30 | 2015-02-05 | 国立大学法人東北大学 | Method for recovering zinc from electric-furnace steelmaking dust and device for recovering zinc from electric-furnace steelmaking dust |
JPWO2015016086A1 (en) * | 2013-07-30 | 2017-03-02 | 国立大学法人東北大学 | Zinc recovery method from electric furnace steelmaking dust and zinc recovery device from electric furnace steelmaking dust |
IT201900018917A1 (en) * | 2019-10-15 | 2021-04-15 | Soprin S R L | SINGLE-DOSE CAPSULE FOR GALVANIZING BATHS |
WO2021074844A1 (en) * | 2019-10-15 | 2021-04-22 | Soprin S.R.L. | Single-dose capsule for galvanizing baths |
US20230175110A1 (en) * | 2019-10-15 | 2023-06-08 | Soprin S.R.L. | Single-dose capsule for galvanizing baths |
CN113122791A (en) * | 2021-04-12 | 2021-07-16 | 中山市华锌工材料科技有限公司 | Metal powder block and preparation method thereof and preparation method of hot-dip galvanizing alloy bath |
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