FI128696B - Process for production of a fertilizer comprising potassium sulfate - Google Patents
Process for production of a fertilizer comprising potassium sulfate Download PDFInfo
- Publication number
- FI128696B FI128696B FI20175682A FI20175682A FI128696B FI 128696 B FI128696 B FI 128696B FI 20175682 A FI20175682 A FI 20175682A FI 20175682 A FI20175682 A FI 20175682A FI 128696 B FI128696 B FI 128696B
- Authority
- FI
- Finland
- Prior art keywords
- ash
- water
- potassium
- precipitator
- potassium chloride
- Prior art date
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Classifications
-
- C—CHEMISTRY; METALLURGY
- C05—FERTILISERS; MANUFACTURE THEREOF
- C05D—INORGANIC FERTILISERS NOT COVERED BY SUBCLASSES C05B, C05C; FERTILISERS PRODUCING CARBON DIOXIDE
- C05D1/00—Fertilisers containing potassium
- C05D1/02—Manufacture from potassium chloride or sulfate or double or mixed salts thereof
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- C—CHEMISTRY; METALLURGY
- C05—FERTILISERS; MANUFACTURE THEREOF
- C05F—ORGANIC FERTILISERS NOT COVERED BY SUBCLASSES C05B, C05C, e.g. FERTILISERS FROM WASTE OR REFUSE
- C05F7/00—Fertilisers from waste water, sewage sludge, sea slime, ooze or similar masses
- C05F7/02—Fertilisers from waste water, sewage sludge, sea slime, ooze or similar masses from sulfite liquor or other waste lyes from the manufacture of cellulose
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- D—TEXTILES; PAPER
- D21—PAPER-MAKING; PRODUCTION OF CELLULOSE
- D21C—PRODUCTION OF CELLULOSE BY REMOVING NON-CELLULOSE SUBSTANCES FROM CELLULOSE-CONTAINING MATERIALS; REGENERATION OF PULPING LIQUORS; APPARATUS THEREFOR
- D21C11/00—Regeneration of pulp liquors or effluent waste waters
-
- D—TEXTILES; PAPER
- D21—PAPER-MAKING; PRODUCTION OF CELLULOSE
- D21C—PRODUCTION OF CELLULOSE BY REMOVING NON-CELLULOSE SUBSTANCES FROM CELLULOSE-CONTAINING MATERIALS; REGENERATION OF PULPING LIQUORS; APPARATUS THEREFOR
- D21C11/00—Regeneration of pulp liquors or effluent waste waters
- D21C11/0007—Recovery of by-products, i.e. compounds other than those necessary for pulping, for multiple uses or not otherwise provided for
-
- D—TEXTILES; PAPER
- D21—PAPER-MAKING; PRODUCTION OF CELLULOSE
- D21C—PRODUCTION OF CELLULOSE BY REMOVING NON-CELLULOSE SUBSTANCES FROM CELLULOSE-CONTAINING MATERIALS; REGENERATION OF PULPING LIQUORS; APPARATUS THEREFOR
- D21C11/00—Regeneration of pulp liquors or effluent waste waters
- D21C11/06—Treatment of pulp gases; Recovery of the heat content of the gases; Treatment of gases arising from various sources in pulp and paper mills; Regeneration of gaseous SO2, e.g. arising from liquors containing sulfur compounds
- D21C11/063—Treatment of gas streams comprising solid matter, e.g. the ashes resulting from the combustion of black liquor
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- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Environmental & Geological Engineering (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Inorganic Chemistry (AREA)
- Processing Of Solid Wastes (AREA)
- Fertilizers (AREA)
Abstract
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Description
POTASSIUM SULFATE Field of the invention The present invention relates to a process for providing value adding products from precipitator ash from a pulp mill.
Background Pulp mills are working continuously to minimize the emissions to air and water and at the same time they aim at recycling process essential chemicals like sodium sulfate which helps to reduce the pulp mills’ operating costs. Therefore the pulp mills preferably recycle the precipitator ash containing sodium sulfate to the mill's "caustic cycle”. However, as the ash contains also non-desirable elements like chlorides and potassium these are accumulated in the mill and at too high levels they negatively influence the process and therefore it is not possible to recycle all precipitator ash to the — pulp mill. Pulp mills continuously monitor the sodium/sulfur balance. The sodium/sulfur balance and the levels of chloride and potassium in the mills are controlled by recycling or discharging precipitator ash, or forwarding the precipitator ash to an ash treatment process if present in the mill. The balance of chemicals in the mill is important as too high levels of potassium and chloride results in process related problems such as corrosion due to chlorides and fouling in the boiler due to potassium. The precipitator ash often removed from the pulp mills and is deposited N to landfills or dissolved in water and forwarded to drains. Since the D precipitator ash contains high levels of sodium sulfate and sodium carbonate . 25 which are chemicals used in the pulp mill discharging too much ash will = directly affect the pulp mill's operating cost since the loss of these chemicals A has to be replaced with new chemicals. E Today there are processes that treat the precipitator ash and remove A non-desirable process elements such as chloride and potassium in order to O 30 be able to recycle the sodium sulfate content of the ash back to the process. = However, such solutions are not able to recycle all sodium sulfate as there N always is a need to discharge a certain amount of the sodium sulfate containing reject e.g. to the drain and therefore not all the process valuable chemicals in the ash can be recycled and large amounts are e.g. forwarded to the drain through a bleed stream or reject. For pulp mills that do not have an ash treatment system the levels of non-desirable process elements are controlled by means of forwarding the precipitator ash to e.g. the drain. Below are different known processes for precipitator ash handling or treatment disclosed.
The precipitator ash may be recycled to the pulp mill directly. The amount of ash that is possible to recycle is limited by the amount of non- desirable process elements, such as potassium and chlorides, and the mill's —sodium/sulfur balance. The pulp mills try to recycle as much precipitator ash as possible but due to the non-desirable process elements in the ash, recycling all the ash will accumulate these undesirable elements. Too high levels of chlorides will result in corrosion of the equipment and too high levels of potassium results in undesirable fouling/scaling in the black liquor boiler.
If the pulp mill is not able to recycle the precipitator ash, it may be forwarded to landfill. This is of cause an additional cost in addition to the loss of valuable process chemicals.
If the pulp mill is not able to recycle the precipitator ash, it may be dissolved in water and forwarded to the wastewater system.
One alternative is also to partly dissolve the precipitator ash in water, possibly including a pH adjustment using sulfuric acid, and separate the non- dissolved ash and the liquid. The non-dissolved ash free from chlorides and potassium is then returned to the pulp mill and the liquid rich in chlorides and potassium, i.e. reject, is sent to the wastewater system.
Another alternative is to dissolve the precipitator ash and then cool it N with ice and where after separation of sodium salts together with crystalline D water may be made. This process primarily removes chlorides from the ash.
. Since the solubility of sodium sulfate decreases with a lower temperature a = solid phase consisting of sodium sulfate and crystalline water is formed. The A 30 solid phase is removed and recycled back to the pulp mill and the liquid E phase containing most of the chlorides is sent to the wastewater system.
A Another alternative is to dissolve the precipitator ash in water and then O evaporating/crystallizing the dissolved sodium salts and separation of the = salts. With this process chlorides and potassium are removed from the N 35 —precipitator ash by first dissolving the ash in water and then forward the solution to an evaporator/crystallizer in order to remove water and increase the concentration to precipitate sodium salts which forms a solid phase which are removed and returned to the pulp mill. The liquid phase containing most of the chlorides and potassium together with dissolved sodium salts is continuously discharged in order to keep the levels of chlorides and potassium at a level inside the crystallizer which is economically viable and not resulting in corrosion.
A problem with the presently known technologies is that none of the techniques utilizes all the ash. In reality a large amount of chemicals is always discharged to landfill or wastewater system even for solutions where the precipitator ash is treated and cleaned from non-desirable process elements and is recycled. At optimum conditions and in theory it is possible to recover about 90% of the precipitator ash by means of such an ash treatment system but in reality the values are much lower, close to about 50% is mentioned in literature and expressed by users.
Today also much focus is put on obtaining environmentally sustainable processes and obtaining as much value adding products or recyclable products out of a process as possible, in order to avoid as much waste and losses as possible.
Thus, there is a need to obtain more efficient processes. There is a demand for processes which reduce the need for putting material on landfills and discharging valuable chemicals to wastewater system. There is also a need for providing additional value adding products from waste material from pulp mills which improves the economy of the total pulp mill.
Summary N With the present process high value products are obtainable and at the D same time as much chemicals as possible form the process may be recycled . back into the pulp mill process to provide an environmentally more = sustainable solution to waste handling. By reusing chemicals and also A 30 providing an added value product that may be sold the total economy of a E pulp mill is improved and the recourses of Mother Nature are used with care. A Precipitator ash which today is forwarded to landfill or the wastewater O system may be treated with potassium chloride in order to create a high value = fertilizer, KoSO4, and a byproduct, NaCl, which may be used in different N 35 applications e.g. road salt.
With the invention almost all chemicals present in the precipitator ash can be used and the negative environmental impact from the pulp mill precipitator ash can be eliminated. Since a high grade fertilizer is obtained by the present invention is it also possible to forward the nutrient chemicals back to the plants where they are needed instead of letting them out to a drain.
This way, nutrients which are removed from the land, e.g. in view of the logging, may be reintroduced with the obtained fertilizer.
The invention may be applied and implemented to any pulp mill that bleed out ash or treat ash in an ash treatment system and the present invention does not negatively affect the pulp mill in any way since it is an "end of pipe solution”.
The present invention relates to a process for producing a fertilizer comprising potassium sulfate, K;SO4 from precipitator ash from a pulp mill, wherein precipitator ash from a pulp mill is provided; water is provided; potassium chloride is provided; and a mixture is provided comprising said water, potassium chloride and precipitator ash, and is allowed to react, wherein potassium sulfate is obtained.
According to one embodiment the potassium chloride and the precipitator ash of the mixture are in any order or simultaneously. Preferably the water and precipitator ash are added before the potassium chloride.
According to one embodiment acid is admixed to the mixture. Preferably sulfuric acid and/or hydrochloric acid is used, more preferably sulfuric acid. Preferably the acid is added before the addition of the potassium chloride.
According to one embodiment the precipitator ash has been pretreated N with the water in an ash treatment process and the reject of the ash treatment D process is contacted with the potassium chloride.
. According to one embodiment sodium hydroxide and/or potassium = hydroxide is added to the water, potassium chloride, and precipitator ash A 30 mixture. This is done to adjust the pH, e.g. if acid has been added.
E According to one embodiment glaserite is obtained by the reaction of A the water, the potassium chloride and the precipitator ash, said glaserite is O removed and admixed with additional potassium chloride and/or is leached = with water to provide potassium sulfate. The potassium sulfate may then be N 35 removed for further use or sold. It is to be noted that the admixing of potassium chloride and leaching with water may be done in any order.
However, in a preferred embodiment the reaction with potassium chloride is performed first followed by leaching with water.
According to one embodiment the remaining mixture after removal of potassium sulfate is concentrated, where after any sodium chloride present is 5 removed for further use.
According to one embodiment the removed sodium chloride is forwarded to a cell membrane process converting it to sodium hydroxide, hydrogen and chlorine.
The present invention also relates to use of the present process for the production of a fertilizer comprising potassium sulfate.
Short description of the drawings Figure 1 discloses a schematic embodiment of the present process. Detailed description Precipitator ash is mixed with and at least partially dissolved in water. Preferably all precipitator ash is dissolved. The aqueous mixture of the precipitator ash may optionally be treated with an acid, preferably sulfuric acid. The optional use of acid may depend on the composition of the precipitator ash. The acid may be used to decrease the amount of carbonates present in the end product. It is to be noted that it is not necessary to remove all carbonates present. If some carbonates are removed using acid the final end product has a higher degree of potassium sulfate, i.e. more pure product. The amount of sulfuric acid which may be added to the mixture in order to convert carbonates of the precipitator ash into carbon dioxide (CO), sulfates N and water depends on the amount of carbonates in the ash and the reguested Oo quality of the end product, potassium sulfate (K.SO,). Acid may be used in an . eguivalent molar ratio with regards to the carbonates present. As an example = a molar ratio of 1:1 of sulfuric acid to carbonate may be used. It is to be A 30 understood that sulfuric acid is not used when not being needed.
E As alternative, the ash may have been pretreated in an ash treatment A process step and the reject there from is used. In such an ash treatment O process the ash is mixed with and at least partially dissolved in water. Non- = desirable process elements for the pulp mill may then be removed as a reject N 35 (ableed stream) and this reject contains dissolved ash in water. This solution may contain the following ions: sodium, sulfates, carbonates, potassium and chlorides. In the pretreatment step the desirable process elements, such as NaSO, and NaOH, may be recycled to the pulp mill process. If needed this pretreated ash mixture reject may be further treated with sulfuric acid in order to decrease and minimize the amount of carbonates in the solution. Sulfuric acid may be added to the pretreated ash mixture reject to react with carbonates present and form sulfate ions, water and carbon dioxide.
Precipitator ash is obtained in the pulp mill process from the black liquor boiler. Precipitator ash from the pulp mill contains mostly sodium, sulfate, and carbonate in various amounts but also small amounts of potassium and chlorides, as well as trace amounts of several metals and elements.
The precipitator ash may vary in chemical content and can roughly be divided into so called low and high carbonate ash depending on the composition.
Below are examples of different precipitator ash contents. Table 1. Precipitator ash content General Low Low High High range for carbonate carbonate carbonate carbonate precipitator | precipitator | precipitator | precipitator | precipitator ash ash ash ash ash (general (a specific (general (a specific range) embodiment) range) embodiment) ~ 3 a - The carbonate content of the ash mixture is adjusted or eliminated by = 20 means of adding sulfuric acid. N Optionally a subseguent step of pH modification using an alkaline O compound may be used, e.g. if the above mentioned acid has been added in D the process. Preferably KOH and/or NaOH are used as alkaline compounds. N The addition of alkaline compound may be used to increase the pH and achieve a correct stoichiometric relation with regards to K,SO4 and NaCl.
Potassium chloride, KCI, is added to the aqueous mixture comprising the precipitator ash in order to obtain potassium sulfate. The solid phase obtained in the process may comprise a salt called glaserite composed of potassium and sodium sulfate (KsNa(SO4),). In one embodiment the intermediate product obtained in the present process after the first addition of the potassium chloride is glaserite.
The obtained glaserite salt is removed from the mother liquor, the liquid remaining part of the mixture, and may be further treated with KCI in order to produce K.SO.. The obtained KSO, may thereafter be removed.
The reactions for the production of the intermediate glaserite and the KSO. are disclosed below. Glaserite: 6 KCl + 4 Na;S04, > 2 K3Na(SO,), + 6 NaCl KSO: 2 KCl + 2 KsNa(SO4)> > 4 KSO, + 2 NaCl As an alternative processing, the obtained glaserite salt may after removal from the mother liquor be leached in water in order to provide K,SO4.
However, in a further embodiment, the present process may include a combination of both mentioned treatment steps for the glaserite, in any order. Then the obtained glaserite salt may first be treated with KCI and thereafter leached in water in order to produce KSO, or the other way around.
The mother liquor remaining after the separation of K;SO4 may be further processed, e.g. via a cooling step in order to precipitate sodium sulfate ~~ and improve the yield of sulfates by returning said sulfates to the pulp mill > process. = The mother liquor remaining after the separation of K;SO4 may be N 30 further processed, e.g. via evaporation in order to precipitate sodium chloride (NaCl) which may be removed as a solid phase. The liquor remaining after = such NaCl separation may then be recycled back to the pulp mill process to N maximize the yield of potassium sulfate in said process. O The present invention can further be complemented by the use of a D 35 membrane cell process which may convert the obtained NaCl into NaOH, Hy N and Cl, NaOH is a valuable chemical and used by the pulp mill in the cooking of wood chips and can therefore be fed directly back to the mill. The two other products H> and Cl, may be collected and either used by the pulp mill, e.g. the chlorine bleach process, or sold to third party to improve the economy and profitability of the mill. In this manner more value adding products than the fertilizer produced may be obtained and reused in the pulp mill or other processes or sold.
With reference to Figure 1 it is shown that in step 1 precipitator ash and water are admixed. In one embodiment the precipitator ash and water may be replaced by or combined with the reject from a pretreatment ash processing system. Optionally acid may be added also in step 1, e.g. sulfuric acid.
The ash comprising mixture may optionally be mixed with KOH and/or NaOH in step 2, where the pH of the mixture is raised and the solution may reach the correct stoichiometric relation with regards to K,SO; and NaCl to be obtained. The alkaline compounds may not be needed, e.g. if no acid has been added in step 1.
Thereafter in step 3, the ash mixture is mixed with KCI in order to obtain K2SO4. The process may create a mixed salt of potassium and sodium sulfate, which is called glaserite. This glaserite salt may then be removed and forwarded to the next step 4 where it is allowed to react in a water solution with additional KCI and may then be further leached in water in step 5 in order to create the end product KSO. It is to be noted that any one of steps 4 and 5 may be used alone, or in combination. The KSO, in solid phase is separated from the mother liguor which is recycled. Since ash could also contain carbonates in various amounts depending on its origin and added sulfuric acid, carbonates could also be present in the end-product to some N extent. D The remaining liquid of the steps 3, 4 and 5 may be recycled to the . previous step of the process in counter current flow with the precipitated salts. = In step 3 where glaserite may be formed, the mother liguor from the step is A 30 forwarded to a cooling step 6 in order to precipitate more sulfate salts which E are separated and recirculated back to step 3. A The remaining solution after the cooling step 6, which has a low O amount of sodium sulfate and potassium but also comprises sodium and = chlorides, is sent to an evaporation step 7 where water is removed in order to N 35 increase the salt concentration and to precipitate NaCl as a solid phase and separate salt from the solution. The water driven off in the evaporation step where NaCl is precipitated and removed from the solution, can be recycled to the process to close the system and be used to dilute reject or dissolve new ash. Therefore the process decreases the requirements for additional water.
Remaining solution after the separation of NaCl is recirculated back to the process in step 2 in order to optimize the use of the chemicals and the yield of potassium sulfate.
Almost all reactions occur at room temperature or slightly above and therefore the process according to the present invention is not very energy demanding, except for the evaporation of water in the NaCl precipitation step
7.
A membrane cell process can additionally be added to the present process in order to provide NaOH for the pulp mill from the generated byproduct, NaCl.
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Claims (9)
1. A process for producing a fertilizer comprising potassium sulfate, K,SO4 from precipitator ash from a pulp mill, wherein precipitator ash from a pulp mill is provided; water is provided; potassium chloride is provided; and a mixture is provided comprising said water, potassium chloride and precipitator ash, and is allowed to react, wherein potassium sulfate is obtained.
2. The process according to claim 1, wherein the water, the potassium chloride and the precipitator ash of the mixture are provided in any order or simultaneously, preferably the water and precipitator ash is added before the potassium chloride.
3. The process according to claim 1 or 2, wherein acid is admixed to the mixture, preferably before the addition of the potassium chloride.
4 The process according to any one of claims 1-3, wherein the precipitator ash has been pretreated with the water in an ash treatment process and the reject of the ash treatment process is contacted with the potassium chloride.
5. The process according to any one of claims 1-4, wherein sodium hydroxide and/or potassium hydroxide is added to the water, potassium chloride, and N precipitator ash mixture.
&
6. The process according to any one of claims 1-5, wherein glaserite is = obtained by the reaction of the water, the potassium chloride and the A 30 precipitator ash, said glaserite is removed and admixed with additional E potassium chloride and/or is leached with water to provide potassium sulfate. & O
7. The process according to claim 6, wherein the remaining mixture after = removal of potassium sulfate is concentrated, whereafter any sodium chloride N 35 present is removed.
8. The process according to claim 7, wherein the removed sodium chloride is forwarded to a membrane cell process converting it to sodium hydroxide, hydrogen and chlorine.
9. Use of a process according to any one of claims 1-8 for the production of a fertilizer comprising potassium sulfate.
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Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
SE1451569A SE1451569A1 (en) | 2014-12-17 | 2014-12-17 | Process for production of a fertilizer comprising potassiumsulfate |
PCT/SE2015/051360 WO2016099392A1 (en) | 2014-12-17 | 2015-12-17 | Process for production of a fertilizer comprising potassium sulfate |
Publications (2)
Publication Number | Publication Date |
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FI20175682A FI20175682A (en) | 2017-07-12 |
FI128696B true FI128696B (en) | 2020-10-15 |
Family
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Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
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FI20175682A FI128696B (en) | 2014-12-17 | 2015-12-17 | Process for production of a fertilizer comprising potassium sulfate |
Country Status (4)
Country | Link |
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CA (1) | CA3004882C (en) |
FI (1) | FI128696B (en) |
SE (1) | SE1451569A1 (en) |
WO (1) | WO2016099392A1 (en) |
Families Citing this family (1)
Publication number | Priority date | Publication date | Assignee | Title |
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WO2024059122A1 (en) * | 2022-09-14 | 2024-03-21 | U.S. Borax, Inc. | Fertiliser product |
Family Cites Families (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4215100A (en) * | 1978-05-18 | 1980-07-29 | Antonova Nina V | Method of producing potassium sulfate |
US5549788A (en) * | 1992-07-30 | 1996-08-27 | A. Ahlstrom Corporation | Minimal effluents discharge pulp mill with chemical recovery |
JPH08170288A (en) * | 1994-12-15 | 1996-07-02 | Mitsubishi Heavy Ind Ltd | Removal of sodium salt and potassium salt from caught ash of soda-recovering boiler |
SE9502583D0 (en) * | 1995-07-12 | 1995-07-12 | Eka Chemicals Ab | Leaching process |
SE9603972D0 (en) * | 1996-10-31 | 1996-10-31 | Kvaerner Pulping Tech | Process for making ash consisting mainly of sodium sulphate from a soda boiler |
CA2219550C (en) * | 1996-11-01 | 2008-05-06 | Sterling Canada, Inc. | A method of recovery of chemical compounds from a pulp mill |
SE9700012D0 (en) * | 1997-01-03 | 1997-01-03 | Eka Chemicals Ab | Recovery process in a pulp mill |
US8721837B2 (en) * | 2012-07-26 | 2014-05-13 | Veolia Water Solutions & Technologies North America, Inc. | Method for recovering pulping chemicals and reducing the concentration of potassium and chloride therein |
-
2014
- 2014-12-17 SE SE1451569A patent/SE1451569A1/en unknown
-
2015
- 2015-12-17 FI FI20175682A patent/FI128696B/en active IP Right Grant
- 2015-12-17 WO PCT/SE2015/051360 patent/WO2016099392A1/en active Application Filing
- 2015-12-17 CA CA3004882A patent/CA3004882C/en active Active
Also Published As
Publication number | Publication date |
---|---|
SE537954C2 (en) | 2015-12-01 |
CA3004882C (en) | 2023-03-14 |
CA3004882A1 (en) | 2016-06-23 |
WO2016099392A1 (en) | 2016-06-23 |
SE1451569A1 (en) | 2015-12-01 |
FI20175682A (en) | 2017-07-12 |
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