US2381369A - Processes for separation of asbestos fiber from associated solids - Google Patents
Processes for separation of asbestos fiber from associated solids Download PDFInfo
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- US2381369A US2381369A US434792A US43479242A US2381369A US 2381369 A US2381369 A US 2381369A US 434792 A US434792 A US 434792A US 43479242 A US43479242 A US 43479242A US 2381369 A US2381369 A US 2381369A
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- United States
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- fiber
- diaphragm
- mass
- fibers
- asbestos
- Prior art date
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- 239000000835 fiber Substances 0.000 title description 61
- 239000010425 asbestos Substances 0.000 title description 28
- 229910052895 riebeckite Inorganic materials 0.000 title description 28
- 238000000034 method Methods 0.000 title description 15
- 239000007787 solid Substances 0.000 title description 9
- 238000000926 separation method Methods 0.000 title description 4
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 30
- 239000000725 suspension Substances 0.000 description 23
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 23
- 239000003518 caustics Substances 0.000 description 21
- 239000003513 alkali Substances 0.000 description 19
- 239000003792 electrolyte Substances 0.000 description 10
- 235000011121 sodium hydroxide Nutrition 0.000 description 10
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 9
- 239000000460 chlorine Substances 0.000 description 9
- 229910052801 chlorine Inorganic materials 0.000 description 9
- 239000000203 mixture Substances 0.000 description 9
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 8
- 239000012267 brine Substances 0.000 description 8
- 239000002245 particle Substances 0.000 description 8
- HPALAKNZSZLMCH-UHFFFAOYSA-M sodium;chloride;hydrate Chemical compound O.[Na+].[Cl-] HPALAKNZSZLMCH-UHFFFAOYSA-M 0.000 description 8
- 230000003750 conditioning effect Effects 0.000 description 7
- 238000007865 diluting Methods 0.000 description 6
- 238000005188 flotation Methods 0.000 description 6
- 239000000243 solution Substances 0.000 description 6
- 239000007788 liquid Substances 0.000 description 5
- 239000000463 material Substances 0.000 description 4
- 239000011780 sodium chloride Substances 0.000 description 4
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 3
- 230000005484 gravity Effects 0.000 description 3
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 2
- 229910052783 alkali metal Inorganic materials 0.000 description 2
- 239000010426 asphalt Substances 0.000 description 2
- 239000010439 graphite Substances 0.000 description 2
- 229910002804 graphite Inorganic materials 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- SNICXCGAKADSCV-UHFFFAOYSA-N nicotine Chemical compound CN1CCCC1C1=CC=CN=C1 SNICXCGAKADSCV-UHFFFAOYSA-N 0.000 description 2
- 238000005204 segregation Methods 0.000 description 2
- 238000002791 soaking Methods 0.000 description 2
- WHXSMMKQMYFTQS-UHFFFAOYSA-N Lithium Chemical compound [Li] WHXSMMKQMYFTQS-UHFFFAOYSA-N 0.000 description 1
- BPQQTUXANYXVAA-UHFFFAOYSA-N Orthosilicate Chemical compound [O-][Si]([O-])([O-])[O-] BPQQTUXANYXVAA-UHFFFAOYSA-N 0.000 description 1
- 235000006629 Prosopis spicigera Nutrition 0.000 description 1
- 240000000037 Prosopis spicigera Species 0.000 description 1
- 229920001131 Pulp (paper) Polymers 0.000 description 1
- 102000018210 Recoverin Human genes 0.000 description 1
- 108010076570 Recoverin Proteins 0.000 description 1
- 229910000831 Steel Inorganic materials 0.000 description 1
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 1
- 238000005273 aeration Methods 0.000 description 1
- 238000013019 agitation Methods 0.000 description 1
- 229910001514 alkali metal chloride Inorganic materials 0.000 description 1
- 229910001508 alkali metal halide Inorganic materials 0.000 description 1
- 150000008045 alkali metal halides Chemical class 0.000 description 1
- -1 alkali metal salts Chemical class 0.000 description 1
- 150000001340 alkali metals Chemical class 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 150000001642 boronic acid derivatives Chemical class 0.000 description 1
- 230000005587 bubbling Effects 0.000 description 1
- 159000000007 calcium salts Chemical class 0.000 description 1
- 150000001860 citric acid derivatives Chemical class 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
- 239000010419 fine particle Substances 0.000 description 1
- 150000004679 hydroxides Chemical class 0.000 description 1
- 238000011065 in-situ storage Methods 0.000 description 1
- 238000002347 injection Methods 0.000 description 1
- 239000007924 injection Substances 0.000 description 1
- 229910052744 lithium Inorganic materials 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 238000005325 percolation Methods 0.000 description 1
- 230000035699 permeability Effects 0.000 description 1
- 239000011148 porous material Substances 0.000 description 1
- 235000011118 potassium hydroxide Nutrition 0.000 description 1
- 238000011084 recovery Methods 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 239000002002 slurry Substances 0.000 description 1
- 235000014347 soups Nutrition 0.000 description 1
- 239000010959 steel Substances 0.000 description 1
- 229910021653 sulphate ion Inorganic materials 0.000 description 1
- 238000010792 warming Methods 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C01—INORGANIC CHEMISTRY
- C01F—COMPOUNDS OF THE METALS BERYLLIUM, MAGNESIUM, ALUMINIUM, CALCIUM, STRONTIUM, BARIUM, RADIUM, THORIUM, OR OF THE RARE-EARTH METALS
- C01F5/00—Compounds of magnesium
-
- C—CHEMISTRY; METALLURGY
- C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
- C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
- C04B20/00—Use of materials as fillers for mortars, concrete or artificial stone according to more than one of groups C04B14/00 - C04B18/00 and characterised by shape or grain distribution; Treatment of materials according to more than one of the groups C04B14/00 - C04B18/00 specially adapted to enhance their filling properties in mortars, concrete or artificial stone; Expanding or defibrillating materials
- C04B20/02—Treatment
- C04B20/08—Defibrillating asbestos
-
- C—CHEMISTRY; METALLURGY
- C25—ELECTROLYTIC OR ELECTROPHORETIC PROCESSES; APPARATUS THEREFOR
- C25B—ELECTROLYTIC OR ELECTROPHORETIC PROCESSES FOR THE PRODUCTION OF COMPOUNDS OR NON-METALS; APPARATUS THEREFOR
- C25B13/00—Diaphragms; Spacing elements
- C25B13/04—Diaphragms; Spacing elements characterised by the material
- C25B13/05—Diaphragms; Spacing elements characterised by the material based on inorganic materials
- C25B13/06—Diaphragms; Spacing elements characterised by the material based on inorganic materials based on asbestos
Definitions
- My invention relates more particularly to recovery of asbestos fiber that has been used in the composition of diaphragms serving to separate the anodeand cathode compartments of electrolytic cells; such as those employed in the decomposition of alkali metal chlorides for produc- Such cells commonlyemploygraphite anodes and foraminous steel cathodes. The ends of the anodes are commonly sealedin with bitumen or its equivalent.
- the electrolyte is an aqueous solution of the alkalichloride, commonly sodium chloride. This is fed into the anode compartment of the cell and percolates through the diaphragm, becoming electrolyzed in its passage to a solution containing caustic sodaand undecomposed'sodium chloride.
- This electrolyte always contains more or less
- the diaphragm acts as a .filter
- the graphite slowly disintegrates,jand some of it finds its way. in the form of fine particles intothe electrolyte and thence to the pores of the diaphragm. The elecforeign matter.
- 'trolyte always contains traces of calcium salts, such as the sulphate and silicate. Some of these droxide, which is likewise depositedin the poresof the diaphragm. The surface of the bitumen becomes more or less chlorinated and some of it likewise finds its way into the diaphragm. The result *is that the porosity of the diaphragm gradually diminishes. Eventually a time is reached when it is no longer fit to serve its purpose. replaced by a fresh diaphragm.
- the diaphragm may have been formed of a'sheet of asbestos paper applied by hand, or it 'may have been formed from the loose fiber in situ by the process of U. S. Patents, Nos.
- the material removed is a sodden mass, slimy with caustic soda, salt and finely "granular deposit and black from graphite. Approximately two thirds of thismass represents the original asbestos fiber and one third material that has been gathered during A operation of the cell.
- Asbestos fiber has a specific gravity of 2.1 to
- asbestos may then be readily separated from the other solids and recovered in form suitable for re-use.
- One way of performing the separation may be illustrated by simply shaking up the suspension in a liter graduate, for example.
- the air thus entrained will be found sufiicient to float .the asbestos fiber, leaving the other solids to settle to the bottom.
- the asbestos will give up its flotation charge of air, or if the graduate be subjected to a vacuum, or the water boiled, the asbestos willlose its air immediately. In either case the asbestos will then settle and rest upon the other solids, proving that the segregation is due to flotation, and surface tension phenomena.
- Another way in which the bubbles may be causedto attach themselves tov the fiber is to suspend the fiber in cold water and then heat the suspension. The heating drives out sufficient of theair dissolved in the water to cause flotation of the fiber.
- the asbestos is already gelatinized as it comes from the cell, but it may be desirable to give it a preliminary wash and gelatinize it again by soaking in caustic soda solution before performing the flotation operation, and this is especially true if the mass has been allowed to dry. Instead of subjecting the mass to'apreliminary soaking in caustic soda Solution,
- the entire operation may be conducted in a solution of caustic soda, whichmay also contain sodium chloride, such as a solution containing 200 to 300 grams per liter of NaCl and 90 grams per liter of NaOI-I.
- caustic soda which may also contain sodium chloride, such as a solution containing 200 to 300 grams per liter of NaCl and 90 grams per liter of NaOI-I.
- sodium chloride such as a solution containing 200 to 300 grams per liter of NaCl and 90 grams per liter of NaOI-I.
- the flotation of the asbestos may be assisted by first passing the mass through a beater of the paper pulp type.
- the fibers thus detached from each other may then be placed in the suspension medium, which should be initially cold. By heating the medium slightly, enough air will then be expelled to float the fiber.
- Another method of breaking, up the mass and liberating the foreign matter is to bubble air through the suspension. This not only detaches the fibers from each other, but at the same time,
- the rotary'movemerit may be obtained by causing the fresh liquid to fiow in tangentially'with respect to the suspension.
- fresh suspension of fiber in the liquid may be added continuously.
- the fiber is then continuously floated over the rim and the other solids are continuously removed from the bottom of the vessel. This may be facilitated b making the vessel of conical form, with the apex at the bottom; or in other words, performing the operation in a cone separator.
- the fiber then fioats over the rim and the solids are withdrawn at the apex.
- the suspension may be led into the cone separator cold, and theheating to expel the flotation air from the liquid may be performed in the separator itself, as by direct injection of steam or in asteam jacket.
- the recovered asbestos, inthe formof a slurry may be caught on a 100 to 200 mesh screen, washed, dewatered, and storeddamp; or it may be (dehydrated, degelatinized by heat and stored
- the caustic soda employed in the process if it be necessary to use any beyond :that with which the mass of diaphragm material is naturally wet, is of course recycled and the net consumption is very small.
- any other caustic alkali such as caustic potash or lithium may be used to gelatinize and swell the fiber.
- the alkaline earth hydroxides are likewise inferior to the causticalkali for this purpose. This would seem to indicate that there is some particular virtue for my purposein the alkali metals as such, regardless of the combination in which they may occur.
- the method of recovering and conditioning for re-use asbestos fiber that has been used in the composition of a diaphragm overlying the foraminous cathode of an electrolytic cell producing chlorine and caustic alkali where ithas been in contact with caustic alkaliand brine and become swollen by the gelatinizin action thereof and the diaphragm has accumulated a deposit, includi-ng 1 carbonaceous and calcareous matter filtered or precipitated out of the electrolyte, which comprises agitating the mass with 20 to times its weight of water to detach the fibers from each other and from the particles of foreign matter and cause minute air bubbles to attach themselves selectively .to th individual swollen fibers; diluting the mass still further .until it is in presence of not less than 2,000 times its weight of water; allowing the diluted mass to segregate; and recovering the fibers from the upper .part' of the resulting suspension.
- cluding carbonaceous and calcareous matter filtered, or precipitated out of the electrolyte which comprises agitating the mass with 20 to 100 times its weight of water to detach the fibers from each other and from the particles of foreign matter and cause, minute air bubbles to attach themselves selectively to the individual swollen fibers; dilut- 6.
- the method of recovering and conditioning for re-use asbestos fiber that has been used in the composition of a diaphragmoverlying the foraminous cathode of an electrolytic cell producing ing the massstill further until it is in presence of 2,000 to 5,000 times its weight of water; allowing the diluted mass to segregate; and recovering th fiber from the resulting suspension.
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- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Inorganic Chemistry (AREA)
- Ceramic Engineering (AREA)
- Materials Engineering (AREA)
- Metallurgy (AREA)
- Electrochemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Geology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Structural Engineering (AREA)
- Processing Of Solid Wastes (AREA)
Description
- tion of caustic alkali and chlorine.
' to remove such matter.
Patented Aug. 7, 1945 PROCESSES FOR SEPARATION OF ASBESTOS FIBER. FROM ASSOCIATED soups James S. Sconce, Niagara Falls, N. Y., assig'nor to'Hooker Electrochemical Company, Niagara Falls, N. Y., a corporation of New York No Drawing. Application March 14, 1942,
Serial N0. 434,792
8 Olaims.
My invention relates more particularly to recovery of asbestos fiber that has been used in the composition of diaphragms serving to separate the anodeand cathode compartments of electrolytic cells; such as those employed in the decomposition of alkali metal chlorides for produc- Such cells commonlyemploygraphite anodes and foraminous steel cathodes. The ends of the anodes are commonly sealedin with bitumen or its equivalent. -The electrolyteis an aqueous solution of the alkalichloride, commonly sodium chloride. This is fed into the anode compartment of the cell and percolates through the diaphragm, becoming electrolyzed in its passage to a solution containing caustic sodaand undecomposed'sodium chloride.
This electrolyte always contains more or less The diaphragm acts as a .filter The graphite slowly disintegrates,jand some of it finds its way. in the form of fine particles intothe electrolyte and thence to the pores of the diaphragm. The elecforeign matter.
'trolyte always contains traces of calcium salts, such as the sulphate and silicate. Some of these droxide, which is likewise depositedin the poresof the diaphragm. The surface of the bitumen becomes more or less chlorinated and some of it likewise finds its way into the diaphragm. The result *is that the porosity of the diaphragm gradually diminishes. Eventually a time is reached when it is no longer fit to serve its purpose. replaced by a fresh diaphragm. The diaphragm may have been formed of a'sheet of asbestos paper applied by hand, or it 'may have been formed from the loose fiber in situ by the process of U. S. Patents, Nos. 1,862,244; 1,862,245 and 1,865,152. In any case, the material removed is a sodden mass, slimy with caustic soda, salt and finely "granular deposit and black from graphite. Approximately two thirds of thismass represents the original asbestos fiber and one third material that has been gathered during A operation of the cell.
Asbestos fiber has a specific gravity of 2.1 to
2.8. Inorder to maintain it in suspension for cell itself, having a specific gravity of about 1.2. The fiber would not be expected toremain in suspension in this medium, but in practice it is found that the caustic soda in the suspension medium acts'to gelatinize and swell the fiber,
thus reducing the specific gravity of the fiber tosuch an extent that it will remain in suspension for a substantially longer time than is needed for the operation of forming the dia-.
I have now discovered that in its gelatinized condition minute air bubbles attach themselves very readily to the asbestos fiber, and with aeration these may easily become suificient actually to fioat the fiber to the surface of the suspension liquid, evenwhen this is pure water. Thus, if
' a quantity of the mass be agitated with to 100 The diaphragm is then removed and times its weight of water in such a way as to detach the fibers from .each other, disperse .them throughout the suspension and entrain air, when the agitation is discontinued .the asbestos will rise to the top and the other solids, which are not gelatinized, will settle to the bottom. The
asbestos may then be readily separated from the other solids and recovered in form suitable for re-use.
4 One way of performing the separation may be illustrated by simply shaking up the suspension in a liter graduate, for example. The air thus entrained will be found sufiicient to float .the asbestos fiber, leaving the other solids to settle to the bottom. Uponstanding, the asbestos will give up its flotation charge of air, or if the graduate be subjected to a vacuum, or the water boiled, the asbestos willlose its air immediately. In either case the asbestos will then settle and rest upon the other solids, proving that the segregation is due to flotation, and surface tension phenomena.
Another way in which the bubbles may be causedto attach themselves tov the fiber is to suspend the fiber in cold water and then heat the suspension. The heating drives out sufficient of theair dissolved in the water to cause flotation of the fiber.
It should be noted that the asbestos is already gelatinized as it comes from the cell, but it may be desirable to give it a preliminary wash and gelatinize it again by soaking in caustic soda solution before performing the flotation operation, and this is especially true if the mass has been allowed to dry. Instead of subjecting the mass to'apreliminary soaking in caustic soda Solution,
the entire operation may be conducted ina solution of caustic soda, whichmay also contain sodium chloride, such as a solution containing 200 to 300 grams per liter of NaCl and 90 grams per liter of NaOI-I. However, I find that the segregation is most rapid and positive when the suspension medium is water at to 60 C., and
preferably 50 C., and the concentration of solids .02 to .05 per cent by weight, and preferably .04 per cent.
The flotation of the asbestos may be assisted by first passing the mass through a beater of the paper pulp type. The fibers thus detached from each other may then be placed in the suspension medium, which should be initially cold. By heating the medium slightly, enough air will then be expelled to float the fiber.
Another method of breaking, up the mass and liberating the foreign matter is to bubble air through the suspension. This not only detaches the fibers from each other, but at the same time,
' Way to its rim, the fiber willfioat over the rim,
leaving the other solids behind. The rotary'movemerit may be obtained by causing the fresh liquid to fiow in tangentially'with respect to the suspension.
Instead of adding fresh suspension liquid to float the fiber over the rim, fresh suspension of fiber in the liquid may be added continuously. The fiber is then continuously floated over the rim and the other solids are continuously removed from the bottom of the vessel. This may be facilitated b making the vessel of conical form, with the apex at the bottom; or in other words, performing the operation in a cone separator. The fiber then fioats over the rim and the solids are withdrawn at the apex.
In practice, with a cone separator having a diameter of about four feet and an equal-depth, and a rotary movement of about one rotation in 2 to 3 minutes, the separation is found to be veryefiective. 5
If preferred, the suspension may be led into the cone separator cold, and theheating to expel the flotation air from the liquid may be performed in the separator itself, as by direct injection of steam or in asteam jacket. q The recovered asbestos, inthe formof a slurry, may be caught on a 100 to 200 mesh screen, washed, dewatered, and storeddamp; or it may be (dehydrated, degelatinized by heat and stored The caustic soda employed in the process, if it be necessary to use any beyond :that with which the mass of diaphragm material is naturally wet, is of course recycled and the net consumption is very small.
In place of caustic soda, any other caustic alkali, such as caustic potash or lithium may be used to gelatinize and swell the fiber. Alkali metal halides, as well as many other alkali metal salts, such as the citrates and borates, likewise have a gelatinizing eifect on the fiber, although it is generally inferior to that of caustic soda. The alkaline earth hydroxides are likewise inferior to the causticalkali for this purpose. This would seem to indicat that there is some particular virtue for my purposein the alkali metals as such, regardless of the combination in which they may occur.
When the asbestos to be recovered is derived from caustic soda chlorine cells, which are by far the largest users of asbestos for diaphragm purposes, the cheapest and most available caustic alkali is naturally the caustic soda with which the material is already wet.
The asbestos recovered from cell diaphragm .by my process is so nearly in its original condition that when it is redeposited inthe form of a diaphragm covering the foraminous metal cathode the rate of percolation of the electrolyte through the diaphragm is found to be substantially the same as in the case of diaphragm formed from fiber previously unused for the purpose. Also, the
rate at which the permeability of diaphragms formed from reused fiber diminishes, due to deposits of foreign matter, and consequently the useful life of diaphragms thus constituted, is found to be normal. It is found that '80 per cent of the asbestos applied to the cells may be recovered and reused by my process, thus reducing the net-consumption of asbestos fiber to about one fifth of what it would otherwise be.
I claim as my invention 2' '1. The method of recovering and conditioning for re-use asbestos fiber that has been used in the composition of a diaphragm overlying the foraminous cathode of an electrolytic cell producing chlorine and caustic alkali where ithas been in contact with caustic alkaliand brine and become swollen by the gelatinizin action thereof and the diaphragm has accumulated a deposit, includi-ng 1 carbonaceous and calcareous matter filtered or precipitated out of the electrolyte, which comprises agitating the mass with 20 to times its weight of water to detach the fibers from each other and from the particles of foreign matter and cause minute air bubbles to attach themselves selectively .to th individual swollen fibers; diluting the mass still further .until it is in presence of not less than 2,000 times its weight of water; allowing the diluted mass to segregate; and recovering the fibers from the upper .part' of the resulting suspension.
2. The method of recovering and conditioning for re-use .asbestcs fiber that has been used in the composition of a diaphragm overlying the foraminous cathode of an electrolytic cell producing chlorine and caustic alkali, where it has been in contact with caustic alkali and brine and become swollen by the v.gela-tinizing action thereof and the diaphragm has accumulated a deposit, including carbonaceous and calcareous matter filtered or precipitated out of the electrolyte, which comprises agitating the .mass, while its fibers are still swollen by said elatinizing action, with 20 to 100 times its weight of water to detach the fibers from each other and from the particles of foreign matter and cause minute air bubbles to attach themselves selectively to the individual swollen fibers; diluting the mass still further until it is in presence of not less than 2,000 times its weight of water; allowing the diluted mass to segregate; and recoverin the fibers from the upper part of the resulting suspension.
.3. The method of recovering and conditioning for re-use asbestos fiber that has been .used in the composition of a diaphragm overlying the fora-minous cathode of an electrolytic cell producing chlorine and caustic alkali; where it has been in contact with caustic alkali and brine and become swollen by the gelatinizing action thereof and the diaphragm has accumulated ,a deposit, including carbonaceous and calcareous matter filtered or precipitated out of the electrolyte, which comprises washing the mass; agitating the mass with 20 to ltimes its weight of water rendered a1- kaline' by the addition of caustic alkali thereto, to detach the fibers from each other and from the particles of foreign matter and cause minute air bubbles to attach themselves selectively to the individual swollen fibers; diluting the mass still further until it is in presence of not less than 2,000 times its weight of water; allowing the dilutedmass to segregate; and recovering the fibers from the-upper part of the resulting suspension. I 4. The method of recovering and conditionin forre-use asbestos fiber that has been used in the composition of a diaphragm overlying the foraminous cathode of an electrolytic cell producing chlorine and caustic alkali, where it has been in contact with caustic alkali and brine and become swollen by the gelatinizing actionthereof and the diaphragm has accumulated a deposit, including carbonaceous and calcareous matter filtered or precipitated outof theelectrolyte, which comprises agitating the mass, in contact with air, with 20 to 100 times its weight of water to detach the fibers'from each other and from the particles of foreign matter and cause minute air bubbles to attach .themselves, selectively to the individual swollenfibers; dilutingthe mass still further until it-is in presence of not elss than 2,000 times its I weight of water; allowing the diluted mass to segregate; and recovering th fibers from the upper part of the resulting suspension. 1
5. The method of recovering and conditioning for re-use asbestos fiber that has been used in the composition of a diaphragm overlying the 0- raminous cathode of an electrolytic cell producingchlorine and caustic alkali, where it has been in contact with caustic alkali and brine and become swollen by the gelatinizing action thereof and the diaphragm has accumulated a deposit, including carbonaceous and calcareous matter filtered or precipitated out of the electrolyte, which comprises agitating the mass with 20 to 100 times its weight 'of water to detach the fibers from each otherand from the particles of foreign matter; bubbling air through the mass to cause minute air bubbles to attach themselves selectively to; the
. individual swollen fibers; diluting the mass still further until it is in presence of not less than 2,000 times its weight of water; allowing the di- 'luted mass to segregate; and recovering the fibers from the upper part of the resulting suspension.
chlorine and caustic alkali, where it has been in contact with caustic alkali and brine and become swollen by the gelatinizing action thereof and the diaphragm has accumulated a deposit, including carbonaceous and calcareous matter filtered or precipitated out of the electrolyte, which comprises agitating the mass with 20 to, 100 times its weight of cold water to detach the fibers from each other and from the particles of foreign matter; warming the water to drive air out of solution in it and cause minute air bubbles to attach themselves selectively to the individual swollen fibers; diluting the mass still further until it is in presence of not less than 2,000 times its weight of water; ,allowing the diluted mass to segregate; and recovering the fibers from the upper part of the resulting suspension.
7. The method of recovering and conditioning for re-use asbestos fiber that has been used in the composition of a diaphragm overlying the foraminous cathode of an lectrolytic cell producing chlorine and caustic alkali, where it has been in contact with caustic alkali and brine and become swollen by the gelatinizing action thereof and the diaphragm has accumulated a deposit, in-
cluding carbonaceous and calcareous matter filtered, or precipitated out of the electrolyte, which comprises agitating the mass with 20 to 100 times its weight of water to detach the fibers from each other and from the particles of foreign matter and cause, minute air bubbles to attach themselves selectively to the individual swollen fibers; dilut- 6. The method of recovering and conditioning for re-use asbestos fiber that has been used in the composition of a diaphragmoverlying the foraminous cathode of an electrolytic cell producing ing the massstill further until it is in presence of 2,000 to 5,000 times its weight of water; allowing the diluted mass to segregate; and recovering th fiber from the resulting suspension.
8. The method of recovering and conditioning for re-use asbestos fiber that has been used in the composition of a diaphragm overlying the foraminous cathode of an electrolytic cell producing chlorine and caustic alkali, where it has been in contact with caustic alkali and brine and become swollen by the gelatinizing action thereof and the diaphragm has accumulated a deposit, including carbonaceous and calcareous matter filtered or precipitated out of the electrolyte, which comprises agitating the mass with 20 to 100 times its weight of water to detach the fibers from each other and from the particles of foreign'matter and cause minute air bubbles to attach themselves selectively to the individual swollen fibers; diluting the mass still further until itis in presence of not less than 2,000 times its weight of water; allowing the diluted mass'to segregate at 20 to 0., and recovering the fibers from the upper part of the resulting suspension.
' JAMES S. SCONCE.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US434792A US2381369A (en) | 1942-03-14 | 1942-03-14 | Processes for separation of asbestos fiber from associated solids |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US434792A US2381369A (en) | 1942-03-14 | 1942-03-14 | Processes for separation of asbestos fiber from associated solids |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US2381369A true US2381369A (en) | 1945-08-07 |
Family
ID=23725721
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US434792A Expired - Lifetime US2381369A (en) | 1942-03-14 | 1942-03-14 | Processes for separation of asbestos fiber from associated solids |
Country Status (1)
| Country | Link |
|---|---|
| US (1) | US2381369A (en) |
Cited By (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2520124A (en) * | 1946-03-20 | 1950-08-29 | United Gas Improvement Co | Rock wool mass |
| US2562646A (en) * | 1947-09-04 | 1951-07-31 | Golden State Company Ltd | Manufacture of casein |
| US2983377A (en) * | 1956-07-24 | 1961-05-09 | Shirriff Horsey Corp Ltd | Process and apparatus for cleaning fruit pulp |
| FR2308702A1 (en) * | 1975-04-25 | 1976-11-19 | Solvay | METHOD AND DEVICE FOR THE MANUFACTURE OF A DIAPHRAGM FROM ASBESTOS OF AN ELECTROLYSIS CELL WITH A DIAPHRAGM |
| CN102452791A (en) * | 2010-12-24 | 2012-05-16 | 江苏奥米建材科技有限公司 | Lipophilic mineral composite fiber and preparation method thereof |
-
1942
- 1942-03-14 US US434792A patent/US2381369A/en not_active Expired - Lifetime
Cited By (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2520124A (en) * | 1946-03-20 | 1950-08-29 | United Gas Improvement Co | Rock wool mass |
| US2562646A (en) * | 1947-09-04 | 1951-07-31 | Golden State Company Ltd | Manufacture of casein |
| US2983377A (en) * | 1956-07-24 | 1961-05-09 | Shirriff Horsey Corp Ltd | Process and apparatus for cleaning fruit pulp |
| FR2308702A1 (en) * | 1975-04-25 | 1976-11-19 | Solvay | METHOD AND DEVICE FOR THE MANUFACTURE OF A DIAPHRAGM FROM ASBESTOS OF AN ELECTROLYSIS CELL WITH A DIAPHRAGM |
| CN102452791A (en) * | 2010-12-24 | 2012-05-16 | 江苏奥米建材科技有限公司 | Lipophilic mineral composite fiber and preparation method thereof |
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