WO2024030773A2 - Process for solubilizing calcium carbonate to obtain a solid compound and an alkaline liquid solution - Google Patents
Process for solubilizing calcium carbonate to obtain a solid compound and an alkaline liquid solution Download PDFInfo
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- WO2024030773A2 WO2024030773A2 PCT/US2023/070860 US2023070860W WO2024030773A2 WO 2024030773 A2 WO2024030773 A2 WO 2024030773A2 US 2023070860 W US2023070860 W US 2023070860W WO 2024030773 A2 WO2024030773 A2 WO 2024030773A2
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- Prior art keywords
- water
- alkaline liquid
- solution
- sodium
- calcium
- Prior art date
Links
- 238000000034 method Methods 0.000 title claims abstract description 54
- 239000007787 solid Substances 0.000 title claims abstract description 21
- 239000006193 liquid solution Substances 0.000 title claims abstract description 18
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 title claims description 46
- 229910000019 calcium carbonate Inorganic materials 0.000 title claims description 23
- 150000001875 compounds Chemical class 0.000 title description 2
- 230000003381 solubilizing effect Effects 0.000 title description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 30
- 229910001868 water Inorganic materials 0.000 claims abstract description 30
- 239000000243 solution Substances 0.000 claims abstract description 29
- 239000002904 solvent Substances 0.000 claims abstract description 16
- 238000006243 chemical reaction Methods 0.000 claims abstract description 13
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 claims description 78
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 claims description 41
- 239000000428 dust Substances 0.000 claims description 20
- 229910000029 sodium carbonate Inorganic materials 0.000 claims description 20
- 239000002893 slag Substances 0.000 claims description 17
- 238000002156 mixing Methods 0.000 claims description 15
- AXCZMVOFGPJBDE-UHFFFAOYSA-L calcium dihydroxide Chemical compound [OH-].[OH-].[Ca+2] AXCZMVOFGPJBDE-UHFFFAOYSA-L 0.000 claims description 12
- OSGAYBCDTDRGGQ-UHFFFAOYSA-L calcium sulfate Chemical compound [Ca+2].[O-]S([O-])(=O)=O OSGAYBCDTDRGGQ-UHFFFAOYSA-L 0.000 claims description 12
- 239000000920 calcium hydroxide Substances 0.000 claims description 11
- 229910001861 calcium hydroxide Inorganic materials 0.000 claims description 11
- 239000007788 liquid Substances 0.000 claims description 10
- PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 claims description 8
- 229910052938 sodium sulfate Inorganic materials 0.000 claims description 8
- 235000011152 sodium sulphate Nutrition 0.000 claims description 8
- KKCBUQHMOMHUOY-UHFFFAOYSA-N sodium oxide Chemical compound [O-2].[Na+].[Na+] KKCBUQHMOMHUOY-UHFFFAOYSA-N 0.000 claims description 3
- 229910001948 sodium oxide Inorganic materials 0.000 claims description 3
- 239000012670 alkaline solution Substances 0.000 claims description 2
- 239000000203 mixture Substances 0.000 claims 2
- 150000004679 hydroxides Chemical class 0.000 claims 1
- -1 hydroxy ions Chemical class 0.000 claims 1
- 239000007864 aqueous solution Substances 0.000 abstract description 4
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 26
- 238000004519 manufacturing process Methods 0.000 description 17
- 239000001569 carbon dioxide Substances 0.000 description 13
- 229910002092 carbon dioxide Inorganic materials 0.000 description 13
- 235000008733 Citrus aurantifolia Nutrition 0.000 description 11
- 235000011941 Tilia x europaea Nutrition 0.000 description 11
- 239000004571 lime Substances 0.000 description 11
- 238000013461 design Methods 0.000 description 7
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 6
- 239000004568 cement Substances 0.000 description 6
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 5
- UIIMBOGNXHQVGW-UHFFFAOYSA-M sodium bicarbonate Substances [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 5
- 239000001488 sodium phosphate Substances 0.000 description 5
- 229910000162 sodium phosphate Inorganic materials 0.000 description 5
- RYFMWSXOAZQYPI-UHFFFAOYSA-K trisodium phosphate Chemical compound [Na+].[Na+].[Na+].[O-]P([O-])([O-])=O RYFMWSXOAZQYPI-UHFFFAOYSA-K 0.000 description 5
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 4
- 239000001506 calcium phosphate Substances 0.000 description 4
- 229910000389 calcium phosphate Inorganic materials 0.000 description 4
- 235000011010 calcium phosphates Nutrition 0.000 description 4
- 238000012545 processing Methods 0.000 description 4
- 238000012552 review Methods 0.000 description 4
- 235000002639 sodium chloride Nutrition 0.000 description 4
- QORWJWZARLRLPR-UHFFFAOYSA-H tricalcium bis(phosphate) Chemical compound [Ca+2].[Ca+2].[Ca+2].[O-]P([O-])([O-])=O.[O-]P([O-])([O-])=O QORWJWZARLRLPR-UHFFFAOYSA-H 0.000 description 4
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 3
- 229910000831 Steel Inorganic materials 0.000 description 3
- 239000003513 alkali Substances 0.000 description 3
- ODINCKMPIJJUCX-UHFFFAOYSA-N calcium oxide Inorganic materials [Ca]=O ODINCKMPIJJUCX-UHFFFAOYSA-N 0.000 description 3
- 229910052742 iron Inorganic materials 0.000 description 3
- 239000000047 product Substances 0.000 description 3
- 235000017557 sodium bicarbonate Nutrition 0.000 description 3
- 229910000030 sodium bicarbonate Inorganic materials 0.000 description 3
- 239000011780 sodium chloride Substances 0.000 description 3
- 239000010959 steel Substances 0.000 description 3
- 238000003860 storage Methods 0.000 description 3
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- 229910021529 ammonia Inorganic materials 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- 239000006227 byproduct Substances 0.000 description 2
- 238000001354 calcination Methods 0.000 description 2
- 239000000460 chlorine Substances 0.000 description 2
- 229910052801 chlorine Inorganic materials 0.000 description 2
- 238000007872 degassing Methods 0.000 description 2
- 239000000395 magnesium oxide Substances 0.000 description 2
- CPLXHLVBOLITMK-UHFFFAOYSA-N magnesium oxide Inorganic materials [Mg]=O CPLXHLVBOLITMK-UHFFFAOYSA-N 0.000 description 2
- AXZKOIWUVFPNLO-UHFFFAOYSA-N magnesium;oxygen(2-) Chemical compound [O-2].[Mg+2] AXZKOIWUVFPNLO-UHFFFAOYSA-N 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 238000012986 modification Methods 0.000 description 2
- 230000004048 modification Effects 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- BVKZGUZCCUSVTD-UHFFFAOYSA-M Bicarbonate Chemical compound OC([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-M 0.000 description 1
- 235000019738 Limestone Nutrition 0.000 description 1
- 241000872931 Myoporum sandwicense Species 0.000 description 1
- UIIMBOGNXHQVGW-DEQYMQKBSA-M Sodium bicarbonate-14C Chemical compound [Na+].O[14C]([O-])=O UIIMBOGNXHQVGW-DEQYMQKBSA-M 0.000 description 1
- 238000009621 Solvay process Methods 0.000 description 1
- 241001625808 Trona Species 0.000 description 1
- 229910052783 alkali metal Inorganic materials 0.000 description 1
- 150000001340 alkali metals Chemical class 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- 239000012080 ambient air Substances 0.000 description 1
- 239000002585 base Substances 0.000 description 1
- 229910001570 bauxite Inorganic materials 0.000 description 1
- BRPQOXSCLDDYGP-UHFFFAOYSA-N calcium oxide Chemical compound [O-2].[Ca+2] BRPQOXSCLDDYGP-UHFFFAOYSA-N 0.000 description 1
- 239000000292 calcium oxide Substances 0.000 description 1
- 238000009993 causticizing Methods 0.000 description 1
- 239000000571 coke Substances 0.000 description 1
- 238000012777 commercial manufacturing Methods 0.000 description 1
- 239000013065 commercial product Substances 0.000 description 1
- 230000002860 competitive effect Effects 0.000 description 1
- 238000005260 corrosion Methods 0.000 description 1
- 230000007797 corrosion Effects 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- 239000003599 detergent Substances 0.000 description 1
- 238000005868 electrolysis reaction Methods 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 239000003546 flue gas Substances 0.000 description 1
- 239000012530 fluid Substances 0.000 description 1
- 239000002803 fossil fuel Substances 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 230000002209 hydrophobic effect Effects 0.000 description 1
- 239000012535 impurity Substances 0.000 description 1
- 239000006028 limestone Substances 0.000 description 1
- 239000012528 membrane Substances 0.000 description 1
- 239000010448 nahcolite Substances 0.000 description 1
- 239000000123 paper Substances 0.000 description 1
- 238000005504 petroleum refining Methods 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- 238000001556 precipitation Methods 0.000 description 1
- 238000000746 purification Methods 0.000 description 1
- 239000012266 salt solution Substances 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 239000000344 soap Substances 0.000 description 1
- 239000002594 sorbent Substances 0.000 description 1
- 239000002699 waste material Substances 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
- C01F11/00—Compounds of calcium, strontium, or barium
- C01F11/46—Sulfates
-
- C—CHEMISTRY; METALLURGY
- C01—INORGANIC CHEMISTRY
- C01D—COMPOUNDS OF ALKALI METALS, i.e. LITHIUM, SODIUM, POTASSIUM, RUBIDIUM, CAESIUM, OR FRANCIUM
- C01D1/00—Oxides or hydroxides of sodium, potassium or alkali metals in general
- C01D1/02—Oxides
-
- C—CHEMISTRY; METALLURGY
- C01—INORGANIC CHEMISTRY
- C01D—COMPOUNDS OF ALKALI METALS, i.e. LITHIUM, SODIUM, POTASSIUM, RUBIDIUM, CAESIUM, OR FRANCIUM
- C01D7/00—Carbonates of sodium, potassium or alkali metals in general
- C01D7/02—Preparation by double decomposition
-
- 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
- C01F11/00—Compounds of calcium, strontium, or barium
- C01F11/18—Carbonates
Definitions
- the subject design relates generally to a process that produces an aqueous solution through a remarkably simple but highly effective chemical reaction.
- the aqueous solution is composed of a blended solution with water and an added solubilizer for the reaction.
- the results produce an ionic solid and an alkaline liquid solution which is a useful commercial product.
- the second step involves the use of a reaction chamber within which a solubilizer, such as glycerol is added to calcium hydroxide.
- a solubilizer such as glycerol
- This addition enhances its solubility to reduce flue gases from a fossil fuel power plant and generate calcium carbonate for use in the wet scrubber.
- Various patents and publications including Pub. No. 2010/0251937 Al, WO 2017/029509, and US 2010/0251937 all teach processes consisting of contacting carbon dioxide laden gas with lime in a reactor such that the lime captures carbon dioxide by the formation of calcium carbonate.
- the calcium oxide or lime is regenerated by calcination leading to the formation of fresh lime sorbent and the release of a concentrated stream of carbon dioxide.
- the “regenerated” lime is then recycled for the future capture of carbon dioxide.
- blended solutions that could be mixed to chemically produce important commercial blended solutions.
- sodium bicarbonate, sodium hydroxide, sodium carbonate, sodium phosphate, calcium hydroxide and calcium carbonate are not readily available and/or expensive to buy or produce.
- sodium carbonate is either found naturally or is manufactured from sodium chloride (common salt).
- sodium carbonate There are two main sources of sodium carbonate. They are from salt and calcium carbonate (Solvay process) or made from sodium carbonate and hydrogen carbonate ores (trona and nahcolite mined).
- Sodium carbonate has many uses, for example but not limited to, paper and manufacturing glass.
- the production of sodium carbonate also requires high heat energy and a high array of equipment to complete the process.
- Ammonia is one of the most expensive materials used in the process and any impurities in the ammonia can cause corrosion in various high temperature areas of the process.
- the process also requires mined limestone and coke. All of this adds major costs to the process.
- Sodium hydroxide is another solution that has been used in the capture of CO 2, as set forth in the article published in the WORLD RESOURCE REVIEW vol. 16 NO. 2 noted above. In the noted paper, their process starts with sodium hydroxide ((NaOH). Their attempt to recover sodium hydroxide has a rather involved process, by itself, which adds heavily to their overall costs.
- Sodium hydroxide can be defined as a strong base of an alkali metal. It has varied applications including being used in manufacturing of soap, detergents, paper and many other different chemicals. It is also used in petroleum refining, in laboratories, or in the purification of aluminum ore, bauxite and many more. This has led to manufacturing of sodium hydroxide on an industrial scale.
- chlor-alkali produces sodium hydroxide and chlorine as coproducts. As is well known, this is accomplished by passing an electric current through a salt solution (common sodium chloride). This process has not been used in the United States for many years because it cannot compete with the production of electrolytic sodium hydroxide. Production of electrolytic sodium hydroxide is the preferred version due to the lesser cost over other processes. There are many issues with the production and transportation of sodium hydroxide. The costs of manufacture and transportation are very high due to its corrosiveness and its high viscosity. As is well known with any chemical, its viscosity is inversely related to its temperature.
- a process is provided that chemically mixes water and a blended solution with a solubilizer to produce an ionic solid and an alkaline liquid solution.
- the subject concept is operational to overcome the high costs of competitive processes and to improve their overall functionality.
- Fig. 1 is a partial flow chart and a partial diagrammatic representation of an embodiment of the subject concept
- Fig. 1 A is a partial flow chart and a partial diagrammatic representation of a more detailed concept from the embodiment of Fig. 1;
- Fig. IB is a partial flow chart and a partial diagrammatic representation of another more detailed concept from the embodiment of Fig. 1;
- Fig. 1C is a partial flow chart and a partial diagrammatic representation of yet another more detailed concept from the embodiment of Fig. 1;
- Fig. ID is a partial flow chart and a partial diagrammatic representation of still another more detailed concept from the embodiment of Fig. 1.
- a solution mixing tank 12 receives one blended solution 14 for mixing with a solubilizer 16 and water 18 via line 19 from the pure water tank 20.
- a fluid pump 21 is disposed in the line 19 and controllably delivers water from the water tank 20 to the mixing tank 12.
- the chemical reaction in the mixing tank 12 creates an ionic solid 22 that is delivered by line 24 to an ionic solid tank 26 for commercial use and/or reuse in the process.
- the chemical reaction also creates an alkaline liquid solution 28 that is delivered by line 30 to an alkaline liquid storage tank 32.
- the alkaline liquid solution in the liquid storage tank 32 could be used further as needed or sold commercially.
- the water 18 in the water tank 20 provides greater efficiency if the pH factor of the water 18 is at least a pH factor of 7.
- several different blended solutions and solubilizers could be used in the embodiment of Fig. 1 without departing from the essence of the subject invention.
- FIG. 1A an embodiment is illustrated providing a source of water 18, calcium hydroxide 36 (blended solution), and sodium phosphate 38 (solubilizer).
- the result of the chemical reaction between the calcium hydroxide 36 and the sodium phosphate 38 are calcium phosphate 40 (an ionic solid) and sodium hydroxide 42 (an alkaline liquid solution).
- the calcium phosphate 40 is now available for commercial use.
- the sodium hydroxide 42 is available for additional processing or, if desirable, it could be sold for commercial uses.
- FIG. IB another embodiment is illustrated providing a source of water 18, a calcium carbonate 46 (blended solution), and a sodium phosphate 38 (solubilizer).
- the results of the chemical reaction between the calcium carbonate 46 and the sodium phosphate 38 creates calcium phosphate 40’ (an ionic solid) and sodium carbonate 48 (alkaline liquid solution).
- the calcium phosphate 40’ is now available for commercial use or redirected for use in additional processing.
- the sodium carbonate solution 48 is now available for use in the current or additional processes or available for commercial uses.
- FIG. IC yet another embodiment is illustrated providing a source of water 18, one of calcium hydroxide 36'. a kiln dust, and a furnace slag (blended solution), and one of sodium bicarbonate and sodium carbonate solution 48' (solubilizer).
- the results of the chemical reaction between the respective ones of the calcium hydroxide solution 36'. the kiln dust, and the furnace slag with the one of sodium bicarbonate and sodium carbonate solution 48' creates calcium carbonate 46' (an ionic solid) and a sodium hydroxide solution 42' (alkaline liquid solution).
- the calcium carbonate 46' is now available for use in the current or additional processes or sold for commercial use.
- the sodium hydroxide solution 42' is now available for additional processing (use in one of the current processes) or available for commercial uses.
- Kiln dust are predominately a solid by-product generated during cement and lime kiln production operations while furnace slag is predominantly waste by-products generated during iron and steel manufacturing.
- lime kiln dust (LKD) and cement kiln dust (CKD) various amounts of calcium oxide (CaO) and ' free lime ' are present.
- CaO calcium oxide
- CKD cement kiln dust
- MgO magnesium oxide
- These oxides also react with the sodium carbonate (Na2COs) to produce additional sodium oxide (NaiO), which when mixed in water becomes sodium hydroxide (NaOH).
- Fig. ID still another embodiment is illustrated providing a source of water 18, calcium carbonate 46’ (blended solution), and sodium sulfate 50 (solubilizer).
- the results of the chemical reaction between the calcium carbonate 46’ and the sodium sulfate 50 creates calcium sulfate 54 (an ionic solid) and a sodium carbonate solution 48’ (alkaline liquid solution).
- the calcium sulfate 54 and the sodium carbonate solution 48’ may each be used in one of the current processes or sold for other commercial uses.
- the subject process with the various examples provides simple, safe, cost-effective designs for producing the alkaline liquid solutions and ionic solid for use in the current or additional processes and/or sold for other commercial uses.
- the subject designs far exceed the other suppliers of these products in production cost effectiveness, more secure ways of storing the products, and in many applications, not needing to store the product but keep redirecting it for other application on site.
- kiln dust or furnace slag With use of kiln dust or furnace slag in the subject process, large volumes of kiln dust or furnace slag will not be stored in huge piles in landfills or used as an aggregate in road projects throughout the country.
- the Federal Highway Administration reported that approximately 14.2 million tons of cement kiln dust (CKD) are produced annually and approximately 2 to 4 million tons of lime kiln dust (LKD) are generated each year in the United States. Furthermore, the FHA also highlighted 15 million tons of furnace slag are also produced per year in the U.S. Most of this kiln dust and furnace slag are disposed of in landfills or stockpiles, with 100 million tons currently stockpiled throughout the country. Even though some of this kiln dust can be sold, and the furnace slag can be used in other manufacturing processes, the cement/lime and iron/steel manufacturing industries still incur high costs for handling the kiln dust and furnace slag. In some applications, the kiln dust and/or furnace slag could be used in another process as it is being generated.
- CKD cement kiln dust
- LLD lime kiln dust
Abstract
The subject process relates generally to producing an aqueous solution through a simple but highly effective chemical reaction. The aqueous solution is composed of a blended solution with water and an added solubilizer for the chemical reaction. The results produce an ionic solid and an alkaline liquid solution which are useful commercial products, and various applications including but not limited to use as a CO2 capture solvent.
Description
Description
PROCESS FOR SOLUBILIZING CALCIUM CARBONATE TO OBTAIN A SOLID COMPOUND AND AN ALKALINE LIQUID SOLUTION
Technical Field R
[0001] The subject design relates generally to a process that produces an aqueous solution through a remarkably simple but highly effective chemical reaction. The aqueous solution is composed of a blended solution with water and an added solubilizer for the reaction. The results produce an ionic solid and an alkaline liquid solution which is a useful commercial product.
Background
[0002] In the past, there has been a lot of discussions with respect to the levels of carbon dioxide (CO2) in the atmosphere. Various attempts have been made by many people to come up with processes to remove the carbon dioxide. For example, US 8,119,091 teaches the use of a multiple step process in which sodium carbonate is treated by casuticization to generate carbon dioxide and sodium oxide. It does not teach the use of sodium hydroxide for the capture of carbon dioxide. US 9,833,739 which issued on Dec. 5, 2017, to Kuku et al teaches the use of a two-step process within which calcium carbonate is used to capture carbon dioxide in a first wet scrubber. The second step involves the use of a reaction chamber within which a solubilizer, such as glycerol is added to calcium hydroxide. This addition enhances its solubility to reduce flue gases from a fossil fuel power plant and generate calcium carbonate for use in the wet scrubber. Various patents and publications including Pub. No. 2010/0251937 Al, WO 2017/029509, and US 2010/0251937 all teach processes consisting of contacting carbon dioxide laden gas with lime in a reactor such that the lime captures carbon dioxide by the formation of calcium carbonate. The calcium oxide or lime is regenerated by calcination leading to the formation of fresh lime sorbent and the release of a concentrated stream of carbon dioxide. The “regenerated” lime is then recycled for the future capture of carbon dioxide. This carbonation calcination process requires heat and the processes are
similar to the methods used in the production of cement worldwide. US 9,981,220 issued to Kuku et.al teaches the use of an acid dosing system for the removal of dissolved CO2 from water, and the precipitation of calcium sulfate in the acid dosing and degassing process. The use of hydrophobic membranes for degassing are known processes.
[0003] In an article published in the WORLD RESOURCE REVIEW vol. 16 NO. 2, the article teaches the desire to remove CO2 directly from the atmosphere. The process starts with an alkaline liquid sodium hydroxide to remove the CO2 from the ambient air which results in sodium carbonate (Na2COs). The sodium carbonate is then mixed with calcium hydroxide to produce sodium hydroxide and calcium carbonate in a process known as causticizing. The calcium carbonate is thermally decomposed, precipitates, washed, and then dried to produce lime (CaO). This process is totally different from the subject design, since in the subject process both an alkaline liquid solution and an ionic solid are being chemically produced.
[0004] There are several different blended solutions that could be mixed to chemically produce important commercial blended solutions. Such as, for example but not limited to, sodium bicarbonate, sodium hydroxide, sodium carbonate, sodium phosphate, calcium hydroxide and calcium carbonate. Several of these blended solutions are not readily available and/or expensive to buy or produce.
[0005] For example, sodium carbonate is either found naturally or is manufactured from sodium chloride (common salt). There are two main sources of sodium carbonate. They are from salt and calcium carbonate (Solvay process) or made from sodium carbonate and hydrogen carbonate ores (trona and nahcolite mined). Sodium carbonate has many uses, for example but not limited to, paper and manufacturing glass. The production of sodium carbonate also requires high heat energy and a high array of equipment to complete the process. Ammonia is one of the most expensive materials used in the process and any impurities in the ammonia can cause corrosion in various high temperature areas of the process. The process also requires mined limestone and coke. All of this adds major costs to the process.
[0006] Sodium hydroxide is another solution that has been used in the capture of CO 2, as set forth in the article published in the WORLD RESOURCE REVIEW vol. 16 NO. 2 noted
above. In the noted paper, their process starts with sodium hydroxide ((NaOH). Their attempt to recover sodium hydroxide has a rather involved process, by itself, which adds heavily to their overall costs. Sodium hydroxide can be defined as a strong base of an alkali metal. It has varied applications including being used in manufacturing of soap, detergents, paper and many other different chemicals. It is also used in petroleum refining, in laboratories, or in the purification of aluminum ore, bauxite and many more. This has led to manufacturing of sodium hydroxide on an industrial scale.
[0007] The current commercial manufacturing technology, referred to as ‘chlor-alkali’, produces sodium hydroxide and chlorine as coproducts. As is well known, this is accomplished by passing an electric current through a salt solution (common sodium chloride). This process has not been used in the United States for many years because it cannot compete with the production of electrolytic sodium hydroxide. Production of electrolytic sodium hydroxide is the preferred version due to the lesser cost over other processes. There are many issues with the production and transportation of sodium hydroxide. The costs of manufacture and transportation are very high due to its corrosiveness and its high viscosity. As is well known with any chemical, its viscosity is inversely related to its temperature. That means the viscosity decreases as temperature increases and the viscosity of sodium hydroxide plays a direct role in its application as well as its storage and transportation. While the ‘chlor-alkali’ process has lower cost advantages, the electric power needed for the electrolysis adds significant costs to process. The electrical costs accounts for 51-58 percent of the ‘chlor-alkali’ production costs when producing sodium hydroxide and chlorine.
[0008] From a review of the above noted prior art, none of the prior art teaches or make obvious the concepts set forth herein. Likewise, in view of the high costs set forth above for previous processes, it is desirable to have a process that overcomes the above problems and shortcomings.
[0009] Other objects, features, and advantages of the subject design will become more apparent from the following detailed description of the following embodiments and certain modifications thereof when taken together with the accompanying drawings.
Summary of the Invention
[0010] According to the present design, a process is provided that chemically mixes water and a blended solution with a solubilizer to produce an ionic solid and an alkaline liquid solution. The subject concept is operational to overcome the high costs of competitive processes and to improve their overall functionality.
Brief Description of the Drawings
[0011] Fig. 1 is a partial flow chart and a partial diagrammatic representation of an embodiment of the subject concept;
[0012] Fig. 1 A is a partial flow chart and a partial diagrammatic representation of a more detailed concept from the embodiment of Fig. 1;
[0013] Fig. IB is a partial flow chart and a partial diagrammatic representation of another more detailed concept from the embodiment of Fig. 1;
[0014] Fig. 1C is a partial flow chart and a partial diagrammatic representation of yet another more detailed concept from the embodiment of Fig. 1; and
[0015] Fig. ID is a partial flow chart and a partial diagrammatic representation of still another more detailed concept from the embodiment of Fig. 1.
Detailed Description
[0016] Referring to Fig. 1 of the drawings, a process 10 is provided. A solution mixing tank 12 receives one blended solution 14 for mixing with a solubilizer 16 and water 18 via line 19 from the pure water tank 20. A fluid pump 21 is disposed in the line 19 and controllably delivers water from the water tank 20 to the mixing tank 12. As the blended solution 14, water 18 and the solubilizer 16 are mixed, a chemical reaction occurs therebetween. The chemical reaction in the mixing tank 12 creates an ionic solid 22 that is delivered by line 24 to an ionic solid tank 26 for commercial use and/or reuse in the process. The chemical reaction also creates an alkaline liquid solution 28 that is delivered by line 30 to an alkaline liquid storage tank 32. It is recognized that the alkaline liquid solution in the liquid storage tank 32 could be used further as needed or sold commercially. The water 18 in the water tank 20 provides greater efficiency if the pH factor of the water 18 is at least a pH factor of 7.
[0017] It is further recognized that several different blended solutions and solubilizers could be used in the embodiment of Fig. 1 without departing from the essence of the subject invention.
Some will be set forth hereafter with respect to the remaining Figs.
[0018] Referring to Fig. 1A, an embodiment is illustrated providing a source of water 18, calcium hydroxide 36 (blended solution), and sodium phosphate 38 (solubilizer). The result of the chemical reaction between the calcium hydroxide 36 and the sodium phosphate 38 are calcium phosphate 40 (an ionic solid) and sodium hydroxide 42 (an alkaline liquid solution). The calcium phosphate 40 is now available for commercial use. Likewise, the sodium hydroxide 42 is available for additional processing or, if desirable, it could be sold for commercial uses.
[0019] Referring to Fig. IB, another embodiment is illustrated providing a source of water 18, a calcium carbonate 46 (blended solution), and a sodium phosphate 38 (solubilizer). The results of the chemical reaction between the calcium carbonate 46 and the sodium phosphate 38 creates calcium phosphate 40’ (an ionic solid) and sodium carbonate 48 (alkaline liquid solution). The calcium phosphate 40’ is now available for commercial use or redirected for use in additional processing. Likewise, the sodium carbonate solution 48 is now available for use in the current or additional processes or available for commercial uses.
[0020] Referring to FIG. IC, yet another embodiment is illustrated providing a source of water 18, one of calcium hydroxide 36'. a kiln dust, and a furnace slag (blended solution), and one of sodium bicarbonate and sodium carbonate solution 48' (solubilizer). The results of the chemical reaction between the respective ones of the calcium hydroxide solution 36'. the kiln dust, and the furnace slag with the one of sodium bicarbonate and sodium carbonate solution 48' creates calcium carbonate 46' (an ionic solid) and a sodium hydroxide solution 42' (alkaline liquid solution). The calcium carbonate 46' is now available for use in the current or additional processes or sold for commercial use. Likewise, the sodium hydroxide solution 42' is now available for additional processing (use in one of the current processes) or available for commercial uses.
[0021] Kiln dust are predominately a solid by-product generated during cement and lime kiln production operations while furnace slag is predominantly waste by-products
generated during iron and steel manufacturing. In both lime kiln dust (LKD) and cement kiln dust (CKD), and furnace slagj various amounts of calcium oxide (CaO) and ' free lime ' are present. Depending on the collection location, (K2O) and magnesium oxide (MgO) can also be present. These oxides also react with the sodium carbonate (Na2COs) to produce additional sodium oxide (NaiO), which when mixed in water becomes sodium hydroxide (NaOH).
[0022] The mixing of the solubilizer with the kiln dust or furnace slag in water, chemically produces calcium carbonate in addition to the alkaline solution. The calcium carbonate is one of the main material inputs necessary for the manufacture of cement and lime, and iron and steel manufacturing. By using kiln dust or furnace slag as a blended solution with or instead of calcium hydroxide, a lot of processing costs will be saved.
[0023] Referring to Fig. ID, still another embodiment is illustrated providing a source of water 18, calcium carbonate 46’ (blended solution), and sodium sulfate 50 (solubilizer). The results of the chemical reaction between the calcium carbonate 46’ and the sodium sulfate 50 creates calcium sulfate 54 (an ionic solid) and a sodium carbonate solution 48’ (alkaline liquid solution). The calcium sulfate 54 and the sodium carbonate solution 48’ may each be used in one of the current processes or sold for other commercial uses.
[0024] By replacing the calcium carbonate 46’ in mixing tank 12 (Fig. ID) with a calcium hydroxide 36, different results are achieved, in that, the ionic solid is the same but the alkaline liquid solution is now a sodium hydroxide solution 42 (alkaline liquid solution). [0025] From a review of the above embodiments, there are numerous combinations of a blended solution mixed with a solubilizer to achieve various results for various uses.
Industrial Applicability
[0026] The subject process with the various examples provides simple, safe, cost-effective designs for producing the alkaline liquid solutions and ionic solid for use in the current or additional processes and/or sold for other commercial uses. The subject designs far exceed the other suppliers of these products in production cost effectiveness, more secure ways of storing the products, and in many applications, not needing to store the product but keep redirecting it for other application on site.
[0027] With use of kiln dust or furnace slag in the subject process, large volumes of kiln dust or furnace slag will not be stored in huge piles in landfills or used as an aggregate in road projects throughout the country. The Federal Highway Administration (FHA) reported that approximately 14.2 million tons of cement kiln dust (CKD) are produced annually and approximately 2 to 4 million tons of lime kiln dust (LKD) are generated each year in the United States. Furthermore, the FHA also highlighted 15 million tons of furnace slag are also produced per year in the U.S. Most of this kiln dust and furnace slag are disposed of in landfills or stockpiles, with 100 million tons currently stockpiled throughout the country. Even though some of this kiln dust can be sold, and the furnace slag can be used in other manufacturing processes, the cement/lime and iron/steel manufacturing industries still incur high costs for handling the kiln dust and furnace slag. In some applications, the kiln dust and/or furnace slag could be used in another process as it is being generated.
[0028] Other embodiments as well as certain variations and modifications of the embodiments herein shown and described will obviously occur to those skilled in the art upon becoming familiar with the underlying concept. It is to be understood, therefore that the subject design, as claimed, may be practiced otherwise than as specifically set forth above.
Claims
1. A process of chemically mixing water and a blended solution with a solubilizer to produce an ionic solid and alkaline liquid solution, the improvement comprising: chemically mixing one of a solution of calcium carbonate and a solution of calcium hydroxide with water and a sodium sulfate alkaline liquid to produce one of a sodium carbonate alkaline liquid and a sodium hydroxide alkaline liquid.
2. The process of claim 1 wherein the chemically mixing of calcium carbonate with water and a blend of sodium sulfate alkaline liquid produces a sodium carbonate alkaline liquid.
3. The process of claim 1 wherein the chemically mixing of calcium hydroxide with water and a blend of sodium sulfate alkaline liquid produces a sodium hydroxide alkaline liquid.
4. The process of claim 1 wherein the chemical reaction between the calcium carbonate and sodium sulfate also produces an ionic solid of calcium sulfate.
5. The process of Claim 2 wherein the mixing of the calcium carbonate, water and sodium sulfate produces an ionic solid of calcium sulfate.
SUBSTITUTE SHEET ( RULE 26)
6. The process of Claim 3 wherein the mixing of the calcium hydroxide, water, and sodium sulfate produces an ionic solid of calcium sulfate.
7. A process of chemically mixing water and a blended solution with a solubilizer to produce an ionic solid and an alkaline liquid solution, the improvement comprising: chemically mixing water with one of a kiln dust and a furnace slag with a sodium carbonate to produce a sodium hydroxide alkaline liquid solution and an ionic solid of calcium carbonate.
8. The process of claim 7 wherein mixing water with one of a kiln dust and a furnace slag with sodium carbonate also produces different types of oxides such as sodium oxide.
9. The process of claim 8 wherein the different types of oxides react with water to produce their respective hydroxides which increases the total hydroxy ions in the alkaline solution.
10. The process of claim 1 wherein the water has a pH factor of at least 7.
11. The process of claim 7 wherein the water has a pH factor of at least 7.
12. The process of claim 7 wherein the one of a kiln dust and the furnace slag is the kiln dust.
13. The process of claim 9 wherein the one of a kiln dust and the furnace slag is the furnace slag.
SUBSTITUTE SHEET ( RULE 26)
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US6086842A (en) * | 1996-01-02 | 2000-07-11 | General Electric Company | Recycling of sodium hydroxide and production of gypsum from dry flue gas desulfurization |
US7179438B2 (en) * | 2005-04-20 | 2007-02-20 | Allegheny Energy, Inc. | Methods and apparatus for recovering gypsum and magnesium hydroxide |
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US20220340426A1 (en) * | 2021-04-27 | 2022-10-27 | Global Carbons Emisions Solutions | Process of mixing two compounds to chemically obtain a solid compound and an alkaline liquid solution |
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