US1259486A - Process of recovering potassium salts. - Google Patents
Process of recovering potassium salts. Download PDFInfo
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- US1259486A US1259486A US16747217A US16747217A US1259486A US 1259486 A US1259486 A US 1259486A US 16747217 A US16747217 A US 16747217A US 16747217 A US16747217 A US 16747217A US 1259486 A US1259486 A US 1259486A
- Authority
- US
- United States
- Prior art keywords
- liquor
- coagulum
- magma
- acid
- kelp
- 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
- 238000000034 method Methods 0.000 title description 13
- 159000000001 potassium salts Chemical class 0.000 title description 10
- 241000512259 Ascophyllum nodosum Species 0.000 description 16
- 241001474374 Blennius Species 0.000 description 16
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 16
- 239000007787 solid Substances 0.000 description 14
- 239000002253 acid Substances 0.000 description 12
- WCUXLLCKKVVCTQ-UHFFFAOYSA-M Potassium chloride Chemical compound [Cl-].[K+] WCUXLLCKKVVCTQ-UHFFFAOYSA-M 0.000 description 10
- 238000001704 evaporation Methods 0.000 description 10
- 238000000926 separation method Methods 0.000 description 10
- 239000000463 material Substances 0.000 description 9
- 150000003839 salts Chemical class 0.000 description 9
- 238000002425 crystallisation Methods 0.000 description 8
- 230000008025 crystallization Effects 0.000 description 8
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 7
- 239000000203 mixture Substances 0.000 description 7
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 6
- 239000007788 liquid Substances 0.000 description 6
- 238000005273 aeration Methods 0.000 description 5
- 235000010443 alginic acid Nutrition 0.000 description 5
- 229920000615 alginic acid Polymers 0.000 description 5
- 230000001112 coagulating effect Effects 0.000 description 4
- 230000007935 neutral effect Effects 0.000 description 4
- 239000005416 organic matter Substances 0.000 description 4
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- 239000000701 coagulant Substances 0.000 description 3
- 230000008020 evaporation Effects 0.000 description 3
- 239000011591 potassium Substances 0.000 description 3
- 229910052700 potassium Inorganic materials 0.000 description 3
- 238000003825 pressing Methods 0.000 description 3
- 239000011780 sodium chloride Substances 0.000 description 3
- 239000000783 alginic acid Substances 0.000 description 2
- 229960001126 alginic acid Drugs 0.000 description 2
- 150000004781 alginic acids Chemical class 0.000 description 2
- 239000006227 byproduct Substances 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- 239000013078 crystal Substances 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 238000000605 extraction Methods 0.000 description 2
- 239000008394 flocculating agent Substances 0.000 description 2
- 230000003311 flocculating effect Effects 0.000 description 2
- 235000011389 fruit/vegetable juice Nutrition 0.000 description 2
- 239000007789 gas Substances 0.000 description 2
- 238000002386 leaching Methods 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 150000003112 potassium compounds Chemical class 0.000 description 2
- 238000004537 pulping Methods 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- IXPNQXFRVYWDDI-UHFFFAOYSA-N 1-methyl-2,4-dioxo-1,3-diazinane-5-carboximidamide Chemical compound CN1CC(C(N)=N)C(=O)NC1=O IXPNQXFRVYWDDI-UHFFFAOYSA-N 0.000 description 1
- FHVDTGUDJYJELY-UHFFFAOYSA-N 6-{[2-carboxy-4,5-dihydroxy-6-(phosphanyloxy)oxan-3-yl]oxy}-4,5-dihydroxy-3-phosphanyloxane-2-carboxylic acid Chemical compound O1C(C(O)=O)C(P)C(O)C(O)C1OC1C(C(O)=O)OC(OP)C(O)C1O FHVDTGUDJYJELY-UHFFFAOYSA-N 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
- 241000196324 Embryophyta Species 0.000 description 1
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 1
- 229940072056 alginate Drugs 0.000 description 1
- DIZPMCHEQGEION-UHFFFAOYSA-H aluminium sulfate (anhydrous) Chemical compound [Al+3].[Al+3].[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O DIZPMCHEQGEION-UHFFFAOYSA-H 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 230000001413 cellular effect Effects 0.000 description 1
- 238000005345 coagulation Methods 0.000 description 1
- 230000015271 coagulation Effects 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 239000002657 fibrous material Substances 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- 239000000446 fuel Substances 0.000 description 1
- 230000005484 gravity Effects 0.000 description 1
- 238000000265 homogenisation Methods 0.000 description 1
- 229910052500 inorganic mineral Inorganic materials 0.000 description 1
- NMCUIPGRVMDVDB-UHFFFAOYSA-L iron dichloride Chemical compound Cl[Fe]Cl NMCUIPGRVMDVDB-UHFFFAOYSA-L 0.000 description 1
- 235000010755 mineral Nutrition 0.000 description 1
- 239000011707 mineral Substances 0.000 description 1
- 239000012452 mother liquor Substances 0.000 description 1
- 230000003472 neutralizing effect Effects 0.000 description 1
- 230000020477 pH reduction Effects 0.000 description 1
- 235000011837 pasties Nutrition 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 229940072033 potash Drugs 0.000 description 1
- BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Substances [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 1
- 235000015320 potassium carbonate Nutrition 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- 238000011084 recovery Methods 0.000 description 1
- 238000001953 recrystallisation Methods 0.000 description 1
- 230000000717 retained effect Effects 0.000 description 1
- 239000013535 sea water Substances 0.000 description 1
- 239000000661 sodium alginate Substances 0.000 description 1
- 235000010413 sodium alginate Nutrition 0.000 description 1
- 229940005550 sodium alginate Drugs 0.000 description 1
- 235000011121 sodium hydroxide Nutrition 0.000 description 1
- 150000003467 sulfuric acid derivatives Chemical class 0.000 description 1
- 150000007968 uric acids Chemical class 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C01—INORGANIC CHEMISTRY
- C01D—COMPOUNDS OF ALKALI METALS, i.e. LITHIUM, SODIUM, POTASSIUM, RUBIDIUM, CAESIUM, OR FRANCIUM
- C01D3/00—Halides of sodium, potassium or alkali metals in general
- C01D3/14—Purification
- C01D3/16—Purification by precipitation or adsorption
Definitions
- This invention relates to processes of recovering potassium salts; and it comprises a method oftreating kelp wherein kelp which is advantageously freshly cut, is comminuted and submitted to what may be termed a homogenizing or pulping treatment, the raw pulp is treated with a little acid or the like to neutralize it and cause a separation of liquor from the insoluble solidsand this liquor is directly evaporated to obtain 0- tassium chlorid; all as more fully herelnafter set forth and as claimed.
- the potassium content of the seaweed is for the most part in solution and while there are many organic comme to treat. It may, however, be kept in seawater until needed, or until decay of the This seaweed I comminute and pulp as finely as possible, giving me a more on less pasty mixture. I have found that if this mixture in a raw state be treated with a little acid or other astringent, just about enough to neutrallze it so as to give a neutral indication to neutral tint litmus, the algin substances separate carrying with them practically all the organic matter and many of the mineral matters which are not here desired. I find it preferable to use hydrochloric acid although sulfuric acid or other coagulating agents may be employed.
- the seaweed as it is cut consists of leaves and stems and may be of several difierent varieties. Some portions of the mass. lend themselves to filtration operations more readily than others and I findit advanta- .pounds of more or less gummy or slimy nageous therefore to treat the seaweed 'in a methodical manner in performing the above stated operation. It is best to take the fresh seaweed and chop or'cut it as fine as practicable, consistent with easy operation, and
- magma After the acidification, the magma separates into two portions, an underlying layer of liquid and a floating blanket of coagulum. I may allow the mass to stand for several hours to promote this separation, or whatis much the same, I may deliver acid. treated magma continuously into the top of a tank while slowly and continuously withdrawing clarified liquor at the bottom. Floating of the coagulum is largely due to entangled air and gases; it will again fall if the magma be allowed to stand too long. For this reason the coagulating treatment is best efiected at once after mincing.
- the settled liquor may be sent directly to multiple effects and evaporated to the crystallizing point, giving a crop of salts rich in potassium chlorid and containing only a minor amount of sodium chlorid. These crystallized salts may be afterward treated in ordinary ways to obtain pure potassium chlorid.
- the liquor is so free of organic matter and scale giving constituents that after crystallization is effected the separated salts may be drained in a centrifugal and the mother liquor returned fo'rreevaporation.
- the blanket formed in the flocculating or coagulating stage because of its physical properties is rather difficult to press; and it' is better to rely on natural separation to effect the recovery of the liquor contained in it. It may however be drained on perfo-.
- a better rated plates, wire gauze, etc. method of disposition is to return it to the minced mass going through the coned presses.
- its solid matters are in large part separated by and with the coarser more or less fibrous matters ofthe original minced pulp or magma, separating the blanket of coagulum from the-clear liquor 'and returning the coagulum to fresh minced material for repassage through the presses, and directly evaporating the separated liquor to produce crystallized potassium chlorid.
- the Solid matter separated in the coagulating operation may be treated to regain valuable byproducts.
- the composition of the blanket depends somewhat upon the particular way in which the mincing operation is conducted. If the blanket be returned to the coned, perforated homogenizer i e way hereinbefore mentioned, the solid matters discharged by the homogenizer will of course be a mixture of the fiber-like material and of coagulum. If it be so returned the coagulum solids will not contain so much of the fibrous matter.
- the solids of the separated blanket may be regarded as consisting of cellular tissue or woody matter, separated alginates and other lessdefinite substances. By treating it with .a little caustic soda (other alkalis seem to be less satisfactory) the alginic acid goes into solution.
- a clear solution of sodium alginate may be produced. This may be evaporated down to give a salt-like complex or alginate. Or it may be acidulated with sulfuric acid throwing alginic acid out of about 190 gallons of clear juice may be obtained from a ton.
- a sortof magma is obconcentrated acid, a rapid coagulation .takes place, giving a blanket of separated solids and a layer of clear juice or liquor. Whether the blanket goes to the top or settles, depends largely upon the mechanioal means employed in mincing and the like.
- Floating is caused by included air and gases, and it is better to work in such a manner that there is considerable aeration during the pulping in order to produce a floating blanket. As stated, it is diflicult to separate the liquor and the coagulum by ordinary mechanical means,such as pressing, and the.
- the floating blanket of coagulum will appear to occupy about 30 per cent. of the total volume.
- This liquid runs about 1.035 specific gravity. It may be less and it may be greater but generally is of about thisaiensity. With such a density the liquor will contain around 6 per cent. of total solids of which perhaps 1 per cent. will be residual organic matter. is potassium chlorid.
- the ratio of KCl to NaCl is about 2: 1; that is with such a liquor containing about 6 per cent. total solids and 3 per cent. KCl, there will be about 1.5 per cent. NaCl.
- the amount of organic matter in solution is generally, after the treatment described not to exceed 1 per cent, an amount which is not great enough to interfere materially with evaporation and crystallizatiom
- the liquor upon evaporation may be made to yield successive crops of crystals.
- the particular composition of About half the solid matter usuallyeach crop of course depends upon the circumstances of evaporation and the tempera: ture at which crystallization takes place, it being borne in mind that KCl is more soluble in hot liquor than in cold while NaCl is of even less solubility in hot liquids than in cold liquids, when the solution also contains much KCl.
- Potassium chlorid may be readily separated by recrystallization in a commercially pure state, and very readily, by treating known amounts of the mixed salts with definite amounts of water at alternating hot and cold temperatures.
- the various crops of crystals obtained maybe readily drained in a centrifugal.
- What I claim is 1.
- the process of recovering potassium salts from kelp which comprises mincing the kelp to form a magma, treating the magma thus produced with an acid agentin merely the quantity sufficient to flocculate suspended solids and produce a coagulum, separating the coagulum and the liquor, and evaporating the liquor to crystallization 2.
- the process of recovering potassium salts from kelp which comprises mincing the kelp to form a magma, treating the magma thus produced with hydrochloric acid in merely the quantity sufiicient to flocculate suspended solids and produce a coagulum, separating the coagulum and the liquor, and evaporating the liquor to crystallization.
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Inorganic Chemistry (AREA)
- Edible Seaweed (AREA)
Description
Ito Drawing.
or sans mm safes.
FRANK'K. CAMERON, OF SALT LAKE CITY, UTAH, ASSIGN'OR TO ALASKA PRODUCTS COMPANY, OF NEW YORK, N. Y., A CORPORATION OF SOUTH DAKOTA.
PROCESS OF RECOVERING POTASSIUM SALTS.
aesaaeo.
To all whom it may concern:
Be it known that I, FRANK K. CAMERON, a citizen of the United States, residing at Salt Lake City, in the county of Salt Lake and State of Utah, have invented certain new and useful Improvements in Processes of Recovering Potassium Salts, of which the following is a specification.
This invention relates to processes of recovering potassium salts; and it comprises a method oftreating kelp wherein kelp which is advantageously freshly cut, is comminuted and submitted to what may be termed a homogenizing or pulping treatment, the raw pulp is treated with a little acid or the like to neutralize it and cause a separation of liquor from the insoluble solidsand this liquor is directly evaporated to obtain 0- tassium chlorid; all as more fully herelnafter set forth and as claimed.
The manufacture of potassium salts from seaweed, or kelp, is of course a very old industry, but it was substantially abandoned until recent emergencies raised the price of potash to a high point. This Was because of the cost of. operation. Practically all the propositions involve drying the wet seaweed, either by artificial heat or by sun heat, and then charring or burning the dried material. Seaweed is a wet, very bulky material and-when it is dried by exposure to the air much handling-as well as s ace is required while if it be dried artificially in roasters and the like the consumption of fuel is inordinate. In burning the dried material it is either merely charred or completely burnt. In either case leaching is necessary and this leaching is also expensive.- If the weed be charred the. salts are retained but extraction from the char is diflicult while if burning be complete to get rid of carbon,-much of the available salts is volatilized. For these reasons among others, the extraction of potassium compounds from seaweeds has not proved profitable under modern conditions except 4 where the price of potassium compounds becomes very high. Occasionally it has been proposed to express the seaweed to obtain a liquid which could be evaporated and the residue Specification of Letters Patent.
cell tissue commences.
Patented Mar. is, was.
Application filed May 9, 1917. Serial No. 167,472.
burnt. From the physical character of the seaweed this has not proved successful in practice.
In the present invention I have provided a simple, cheap and ready method of extracting the potassium values from the seaweeds without manual handling and with the recovering of valuable byproducts. I
have. found that the potassium content of the seaweed is for the most part in solution and while there are many organic comme to treat. It may, however, be kept in seawater until needed, or until decay of the This seaweed I comminute and pulp as finely as possible, giving me a more on less pasty mixture. I have found that if this mixture in a raw state be treated with a little acid or other astringent, just about enough to neutrallze it so as to give a neutral indication to neutral tint litmus, the algin substances separate carrying with them practically all the organic matter and many of the mineral matters which are not here desired. I find it preferable to use hydrochloric acid although sulfuric acid or other coagulating agents may be employed.
The seaweed as it is cut consists of leaves and stems and may be of several difierent varieties. Some portions of the mass. lend themselves to filtration operations more readily than others and I findit advanta- .pounds of more or less gummy or slimy nageous therefore to treat the seaweed 'in a methodical manner in performing the above stated operation. It is best to take the fresh seaweed and chop or'cut it as fine as practicable, consistent with easy operation, and
then run the minced mass through some type of pressing device with perforated plates or the like, adapted to retain merely the coarser matter; the fibrous parts and components of the seaweed. Removal of these portions at this stage reduces the amount of coagulum to be subsequently separated; and these portions may also with advantage be used in treating the coagulum itself in a manner hereinafter described. I have found advantageous the type of continuous presses having coned perforated elements. On running the minced mass of seaweed through such a press it is separated into a portion of a more fibrous character which is separated and delivered by the press; and a pulpy-mass or magma which flows or exudes through the perforations. This pulpy mass or magma I place in suitable vats or tanks, and to it I add a little hydrochloric acid. As stated, other coagulating agents may be used but I find that as a rule with most seaweed materials hydrochloric acid gives me the best results. In using hydrochloric acid not much is necessary; I do not ordinarily add enough to produce any distinct acidity. The best results are obtained in using enough hydrochloric acid with the magma to produce aseparated liquor which w1ll appear neutral in reaction to neutral tint litmus paper. The material itself will ind1- cate the right amount of acid since the color, with the right amount, becomes a faded grayish yellow. After the acidification, the magma separates into two portions, an underlying layer of liquid and a floating blanket of coagulum. I may allow the mass to stand for several hours to promote this separation, or whatis much the same, I may deliver acid. treated magma continuously into the top of a tank while slowly and continuously withdrawing clarified liquor at the bottom. Floating of the coagulum is largely due to entangled air and gases; it will again fall if the magma be allowed to stand too long. For this reason the coagulating treatment is best efiected at once after mincing.
There are many other acid reacting coagulating or fiocculating agents which I may use in lieu of hydrochloric or sulfuric acid, such as aluminum sulfate, iron chlorid, etc., for neutralizing the basic bodies present, but they have ordinarily no advantage over hydrochloric acid and furthermore are not as desirable, particularly where suli'uric acid salts are employed, for the reason that I propose regaining my potassium as potassium chlorid as free as may be from sulfates and other salts.
The settled liquor may be sent directly to multiple effects and evaporated to the crystallizing point, giving a crop of salts rich in potassium chlorid and containing only a minor amount of sodium chlorid. These crystallized salts may be afterward treated in ordinary ways to obtain pure potassium chlorid. The liquor is so free of organic matter and scale giving constituents that after crystallization is effected the separated salts may be drained in a centrifugal and the mother liquor returned fo'rreevaporation.
The blanket formed in the flocculating or coagulating stage because of its physical properties is rather difficult to press; and it' is better to rely on natural separation to effect the recovery of the liquor contained in it. It may however be drained on perfo-.
A better rated plates, wire gauze, etc. method of disposition is to return it to the minced mass going through the coned presses. Here its solid matters are in large part separated by and with the coarser more or less fibrous matters ofthe original minced pulp or magma, separating the blanket of coagulum from the-clear liquor 'and returning the coagulum to fresh minced material for repassage through the presses, and directly evaporating the separated liquor to produce crystallized potassium chlorid.
The Solid matter separated in the coagulating operation may be treated to regain valuable byproducts. The composition of the blanket depends somewhat upon the particular way in which the mincing operation is conducted. If the blanket be returned to the coned, perforated homogenizer i e way hereinbefore mentioned, the solid matters discharged by the homogenizer will of course be a mixture of the fiber-like material and of coagulum. If it be so returned the coagulum solids will not contain so much of the fibrous matter. The solids of the separated blanket may be regarded as consisting of cellular tissue or woody matter, separated alginates and other lessdefinite substances. By treating it with .a little caustic soda (other alkalis seem to be less satisfactory) the alginic acid goes into solution. By separating the liquor from the solid matter a clear solution of sodium alginate may be produced. This may be evaporated down to give a salt-like complex or alginate. Or it may be acidulated with sulfuric acid throwing alginic acid out of about 190 gallons of clear juice may be obtained from a ton. On chopping and minc ing the fresh seaweed in the manner hereinbefore described a sortof magma is obconcentrated acid, a rapid coagulation .takes place, giving a blanket of separated solids and a layer of clear juice or liquor. Whether the blanket goes to the top or settles, depends largely upon the mechanioal means employed in mincing and the like. Floating is caused by included air and gases, and it is better to work in such a manner that there is considerable aeration during the pulping in order to produce a floating blanket. As stated, it is diflicult to separate the liquor and the coagulum by ordinary mechanical means,such as pressing, and the.
fact that if the pulp or magma is well aerated the mixture will separate of itself, is of great technical importance. Therefore, the effort should be to employ mechanical means in the mincing step which will give as much aeration as possible. The extent to which the blanket contracts, 2'. 6., the relation between the volume of the blanket and the volume of clear liquor, depends upon the length of time the mixture is allowed to stand after the addition of the acid or other coagulant; the extent of aeration and many other factors. The more intimate and uniform the aeration has been the quicker will be the separation. The ideal condition is to have minute air-bells thoroughly, distributed through the solid matters. Usually, after acidulating and allowing the mass to stand for about 30 minutes, the floating blanket of coagulum will appear to occupy about 30 per cent. of the total volume. By standing longer blanket contracts further and the volume of clear liquid obtained is considerably increased. This liquid runs about 1.035 specific gravity. It may be less and it may be greater but generally is of about thisaiensity. With such a density the liquor will contain around 6 per cent. of total solids of which perhaps 1 per cent. will be residual organic matter. is potassium chlorid. The ratio of KCl to NaCl is about 2: 1; that is with such a liquor containing about 6 per cent. total solids and 3 per cent. KCl, there will be about 1.5 per cent. NaCl. The amount of organic matter in solution is generally, after the treatment described not to exceed 1 per cent, an amount which is not great enough to interfere materially with evaporation and crystallizatiom The liquor upon evaporation may be made to yield successive crops of crystals. The particular composition of About half the solid matter usuallyeach crop of course depends upon the circumstances of evaporation and the tempera: ture at which crystallization takes place, it being borne in mind that KCl is more soluble in hot liquor than in cold while NaCl is of even less solubility in hot liquids than in cold liquids, when the solution also contains much KCl.
Potassium chlorid may be readily separated by recrystallization in a commercially pure state, and very readily, by treating known amounts of the mixed salts with definite amounts of water at alternating hot and cold temperatures.
Any ordinary type of evaporator working under vacuum or under plus pressure, or both, may be employed. It is advantageous to use the ordinary types adapted for the manufacture of salt. The various crops of crystals obtained maybe readily drained in a centrifugal.
What I claim is 1. The process of recovering potassium salts from kelp which comprises mincing the kelp to form a magma, treating the magma thus produced with an acid agentin merely the quantity sufficient to flocculate suspended solids and produce a coagulum, separating the coagulum and the liquor, and evaporating the liquor to crystallization 2. The process of recovering potassium salts from kelp which comprises mincing the kelp to form a magma, treating the magma thus produced with hydrochloric acid in merely the quantity sufiicient to flocculate suspended solids and produce a coagulum, separating the coagulum and the liquor, and evaporating the liquor to crystallization. I
3. The process of recovering potassium salts from kelp which comprises mincing the kelp to form a magma, separating the coarser: and fibrous-like portions of the magma, adding an acid flocculatlng agent to produce coagulum and a separation of liquor, returning the coagulum to fresh minced material'and evaporating the liquor to crystallization.
4. The process of recovering potasslum salts from kelp which comprises mincing the fresh kelp, pressing the mincedmaterial through coarse perforations to produce a homogenized magma with some separation ofcoarse and fibrous material, add
ing an acid flocculating agent to the homogenized magma to produce a coagulum and separation of liquor, returning the coagulum to fresh minced material for separation and homogenization and evaporating the liquor to crystallization.
5. The process of recovering potassium salts from kelp which comprises mincing and straining the kelp in such a manner as to produce thorough aeration, adding an acid flocculating agent to produce a floating separation of coagulum from the clear liquor returning the floating coagulum for treatment together With fresh kelp in the straining operation and evaporating the liquor to crystallization.
6. The process of recovering potassium salts from kelp which comprises comminuting the kelp to form a thoroughly aerated substantially uniform magma, treating this 10- magma With an acid flocculating agentto form a floating separation of air-buoyed solids, and evaporating the separated liquor to crystallization. 4
In testimony whereof, I affix my signature 15 hereto.
FRANK K. CAMERON.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US16747217A US1259486A (en) | 1917-05-09 | 1917-05-09 | Process of recovering potassium salts. |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US16747217A US1259486A (en) | 1917-05-09 | 1917-05-09 | Process of recovering potassium salts. |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US1259486A true US1259486A (en) | 1918-03-19 |
Family
ID=3327168
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US16747217A Expired - Lifetime US1259486A (en) | 1917-05-09 | 1917-05-09 | Process of recovering potassium salts. |
Country Status (1)
| Country | Link |
|---|---|
| US (1) | US1259486A (en) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2715608A (en) * | 1952-04-08 | 1955-08-16 | Niagara Alkali Company | Electrolysis of aqueous solutions of mixtures of potassium and sodium chloride |
-
1917
- 1917-05-09 US US16747217A patent/US1259486A/en not_active Expired - Lifetime
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2715608A (en) * | 1952-04-08 | 1955-08-16 | Niagara Alkali Company | Electrolysis of aqueous solutions of mixtures of potassium and sodium chloride |
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