ZA200906732B - An apparatus for recovering soluble salts - Google Patents
An apparatus for recovering soluble salts Download PDFInfo
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- ZA200906732B ZA200906732B ZA200906732A ZA200906732A ZA200906732B ZA 200906732 B ZA200906732 B ZA 200906732B ZA 200906732 A ZA200906732 A ZA 200906732A ZA 200906732 A ZA200906732 A ZA 200906732A ZA 200906732 B ZA200906732 B ZA 200906732B
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- 150000003839 salts Chemical class 0.000 title claims description 27
- 238000000034 method Methods 0.000 claims description 29
- 150000001875 compounds Chemical class 0.000 claims description 24
- 238000006243 chemical reaction Methods 0.000 claims description 18
- 238000001556 precipitation Methods 0.000 claims description 18
- 239000007864 aqueous solution Substances 0.000 claims description 14
- 229910052782 aluminium Inorganic materials 0.000 claims description 11
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 claims description 11
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 claims description 8
- 150000002500 ions Chemical class 0.000 claims description 8
- 239000000243 solution Substances 0.000 claims description 8
- 230000006698 induction Effects 0.000 claims description 7
- 239000003153 chemical reaction reagent Substances 0.000 claims description 6
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 claims description 5
- 229910052802 copper Inorganic materials 0.000 claims description 5
- 239000010949 copper Substances 0.000 claims description 5
- 239000000463 material Substances 0.000 claims description 5
- 238000003756 stirring Methods 0.000 claims description 5
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 claims description 4
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 claims description 4
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 claims description 4
- 229910052791 calcium Inorganic materials 0.000 claims description 4
- 239000011575 calcium Substances 0.000 claims description 4
- 229910052742 iron Inorganic materials 0.000 claims description 4
- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Chemical compound [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 claims description 4
- 238000001228 spectrum Methods 0.000 claims description 4
- 229910052718 tin Inorganic materials 0.000 claims description 4
- 239000011135 tin Substances 0.000 claims description 4
- 230000015271 coagulation Effects 0.000 claims description 3
- 238000005345 coagulation Methods 0.000 claims description 3
- 239000003245 coal Substances 0.000 claims description 3
- 239000004035 construction material Substances 0.000 claims description 3
- 239000010936 titanium Substances 0.000 claims description 3
- ZOXJGFHDIHLPTG-UHFFFAOYSA-N Boron Chemical compound [B] ZOXJGFHDIHLPTG-UHFFFAOYSA-N 0.000 claims description 2
- 235000008733 Citrus aurantifolia Nutrition 0.000 claims description 2
- CBENFWSGALASAD-UHFFFAOYSA-N Ozone Chemical compound [O-][O+]=O CBENFWSGALASAD-UHFFFAOYSA-N 0.000 claims description 2
- 235000011941 Tilia x europaea Nutrition 0.000 claims description 2
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 claims description 2
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 claims description 2
- 238000007664 blowing Methods 0.000 claims description 2
- 229910052796 boron Inorganic materials 0.000 claims description 2
- 229910003460 diamond Inorganic materials 0.000 claims description 2
- 239000010432 diamond Substances 0.000 claims description 2
- PCHJSUWPFVWCPO-UHFFFAOYSA-N gold Chemical compound [Au] PCHJSUWPFVWCPO-UHFFFAOYSA-N 0.000 claims description 2
- 229910052737 gold Inorganic materials 0.000 claims description 2
- 239000010931 gold Substances 0.000 claims description 2
- 238000002347 injection Methods 0.000 claims description 2
- 239000007924 injection Substances 0.000 claims description 2
- 239000011133 lead Substances 0.000 claims description 2
- 239000004571 lime Substances 0.000 claims description 2
- 229910052759 nickel Inorganic materials 0.000 claims description 2
- 239000002245 particle Substances 0.000 claims description 2
- 229910052697 platinum Inorganic materials 0.000 claims description 2
- 229910052719 titanium Inorganic materials 0.000 claims description 2
- 229910052725 zinc Inorganic materials 0.000 claims description 2
- 239000011701 zinc Substances 0.000 claims description 2
- 229910045601 alloy Inorganic materials 0.000 claims 1
- 239000000956 alloy Substances 0.000 claims 1
- 238000002386 leaching Methods 0.000 claims 1
- 150000003467 sulfuric acid derivatives Chemical class 0.000 description 8
- 239000002244 precipitate Substances 0.000 description 7
- 239000013535 sea water Substances 0.000 description 7
- 150000001805 chlorine compounds Chemical class 0.000 description 6
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 5
- 229910019142 PO4 Inorganic materials 0.000 description 4
- 238000001914 filtration Methods 0.000 description 4
- 230000007246 mechanism Effects 0.000 description 4
- 235000021317 phosphate Nutrition 0.000 description 4
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 3
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 3
- 230000015572 biosynthetic process Effects 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 230000005684 electric field Effects 0.000 description 3
- 229910052935 jarosite Inorganic materials 0.000 description 3
- 238000005065 mining Methods 0.000 description 3
- 230000006911 nucleation Effects 0.000 description 3
- 238000010899 nucleation Methods 0.000 description 3
- 150000003013 phosphoric acid derivatives Chemical class 0.000 description 3
- 229910021653 sulphate ion Inorganic materials 0.000 description 3
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 2
- 229910002651 NO3 Inorganic materials 0.000 description 2
- NHNBFGGVMKEFGY-UHFFFAOYSA-N Nitrate Chemical compound [O-][N+]([O-])=O NHNBFGGVMKEFGY-UHFFFAOYSA-N 0.000 description 2
- 238000010521 absorption reaction Methods 0.000 description 2
- WNROFYMDJYEPJX-UHFFFAOYSA-K aluminium hydroxide Chemical compound [OH-].[OH-].[OH-].[Al+3] WNROFYMDJYEPJX-UHFFFAOYSA-K 0.000 description 2
- 230000008901 benefit Effects 0.000 description 2
- 238000005516 engineering process Methods 0.000 description 2
- 238000005189 flocculation Methods 0.000 description 2
- 230000016615 flocculation Effects 0.000 description 2
- 239000003621 irrigation water Substances 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- 150000002823 nitrates Chemical class 0.000 description 2
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 2
- 239000010452 phosphate Substances 0.000 description 2
- 238000002203 pretreatment Methods 0.000 description 2
- 239000000047 product Substances 0.000 description 2
- 238000001223 reverse osmosis Methods 0.000 description 2
- 239000010865 sewage Substances 0.000 description 2
- 229910052708 sodium Inorganic materials 0.000 description 2
- 239000011734 sodium Substances 0.000 description 2
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 150000001450 anions Chemical class 0.000 description 1
- 159000000009 barium salts Chemical class 0.000 description 1
- 235000012206 bottled water Nutrition 0.000 description 1
- AXCZMVOFGPJBDE-UHFFFAOYSA-L calcium dihydroxide Chemical compound [OH-].[OH-].[Ca+2] AXCZMVOFGPJBDE-UHFFFAOYSA-L 0.000 description 1
- 229910001861 calcium hydroxide Inorganic materials 0.000 description 1
- 239000000920 calcium hydroxide Substances 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 238000006073 displacement reaction Methods 0.000 description 1
- 239000003651 drinking water Substances 0.000 description 1
- 239000003814 drug Substances 0.000 description 1
- 229940079593 drug Drugs 0.000 description 1
- 238000009297 electrocoagulation Methods 0.000 description 1
- 229910001385 heavy metal Inorganic materials 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- 230000003189 isokinetic effect Effects 0.000 description 1
- 238000003760 magnetic stirring Methods 0.000 description 1
- 230000005285 magnetism related processes and functions Effects 0.000 description 1
- 238000010907 mechanical stirring Methods 0.000 description 1
- 239000012528 membrane Substances 0.000 description 1
- 150000002826 nitrites Chemical class 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- 238000011084 recovery Methods 0.000 description 1
- 239000004576 sand Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 230000001131 transforming effect Effects 0.000 description 1
- 239000003643 water by type Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C02—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F1/00—Treatment of water, waste water, or sewage
- C02F1/46—Treatment of water, waste water, or sewage by electrochemical methods
- C02F1/461—Treatment of water, waste water, or sewage by electrochemical methods by electrolysis
- C02F1/463—Treatment of water, waste water, or sewage by electrochemical methods by electrolysis by electrocoagulation
-
- C—CHEMISTRY; METALLURGY
- C02—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F1/00—Treatment of water, waste water, or sewage
- C02F1/48—Treatment of water, waste water, or sewage with magnetic or electric fields
-
- C—CHEMISTRY; METALLURGY
- C02—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F1/00—Treatment of water, waste water, or sewage
- C02F1/52—Treatment of water, waste water, or sewage by flocculation or precipitation of suspended impurities
- C02F1/5236—Treatment of water, waste water, or sewage by flocculation or precipitation of suspended impurities using inorganic agents
-
- C—CHEMISTRY; METALLURGY
- C02—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F1/00—Treatment of water, waste water, or sewage
- C02F1/66—Treatment of water, waste water, or sewage by neutralisation; pH adjustment
-
- C—CHEMISTRY; METALLURGY
- C02—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F1/00—Treatment of water, waste water, or sewage
- C02F1/72—Treatment of water, waste water, or sewage by oxidation
- C02F1/78—Treatment of water, waste water, or sewage by oxidation with ozone
-
- C—CHEMISTRY; METALLURGY
- C02—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F2103/00—Nature of the water, waste water, sewage or sludge to be treated
- C02F2103/08—Seawater, e.g. for desalination
-
- C—CHEMISTRY; METALLURGY
- C02—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F2103/00—Nature of the water, waste water, sewage or sludge to be treated
- C02F2103/10—Nature of the water, waste water, sewage or sludge to be treated from quarries or from mining activities
-
- C—CHEMISTRY; METALLURGY
- C02—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F2201/00—Apparatus for treatment of water, waste water or sewage
- C02F2201/48—Devices for applying magnetic or electric fields
- C02F2201/483—Devices for applying magnetic or electric fields using coils
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02A—TECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE
- Y02A20/00—Water conservation; Efficient water supply; Efficient water use
- Y02A20/124—Water desalination
- Y02A20/138—Water desalination using renewable energy
- Y02A20/144—Wave energy
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Environmental & Geological Engineering (AREA)
- Water Supply & Treatment (AREA)
- Hydrology & Water Resources (AREA)
- Life Sciences & Earth Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Electrochemistry (AREA)
- General Chemical & Material Sciences (AREA)
- Water Treatment By Electricity Or Magnetism (AREA)
- Physical Or Chemical Processes And Apparatus (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Description
. 2879-2008
AN APPARATUS FOR RECOVERING SOLUBLE SALTS
FIELD OF THE INVENTION I | MI
DE
This invention relates to the recovery of soluble salts by turning them insoluble through chemical, electric, and magnetic processes.
There are many processes in the state of the art where chemical reactions result in insoluble products. Other reactions, however, form soluble salts, for which they cannot be separated from an aqueous solution.
The present invention seeks to offer a solution to this technical problem by taking all soluble salts from an aqueous solution and forcing them to form insoluble compounds.
Examples of processes forming insoluble salts are found in the state of the art as follows:
JP2004255627 discloses a process of salt insolubilization as a pre-treatment to prevent membranes from fauling by reverse osmosis. This process does not use any magnetic field nor frequency and cannot insolubilize chlorides or sulphates.
: 2879-2008
US 5858249 discloses a process of insolubilization of ionic species in a kind of : electrolytic cell that works as electro-coagulation to form insoiubles with salts inherently contained in the (aqueous solution, and the addition of ions of the sacrificial electrode. This process cannot precipitate chlorides or sulphates.
CN 1131127 se discloses a process of insolubilization of salts contained in an aqueous solution by adding chemical reagents, such as phosphate salts and barium salts. The precipitate solutions are separated by filtering, the aqueous solution, in this case water, ending up with a low salt content. This process does not apply electric, magnetic or frequency fields and cannot form compounds.
The present invention relates to a process for forming insoluble chemical compounds in a liquid medium by way of physical stimuli. The compounds thus formed can be inorganic or organic, simple or complex. The technical problem addressed by the present invention is that of transforming highly soluble salts into insoluble compounds so that they may be separated from the aqueous solution to obtain a benefit from both the separated salts and the purified residual liquid.
Reactive mechanisms and physical changes take place in a single phase or reactor, such as the initial precipitation of compounds that act as nuclei for subsequent nucleation and absorption mechanisms of other species formed. The formation of these first precipitates is due to the action of an electric and magnetic field applied by
. 2879-2008 #2009/067 32 way of an ultra-filtered electric current transmitted through electrodes, in addition to the ionic contribution by one of the electrodes acting as a sacrificial one.
Thereafter, a second ionic contribution is added, usually aluminum, calcium, iron, lead or tin to form new compounds with the salts contained in the aqueous solution.
The size of the initially formed nuclei is thereby increased by the new compounds and at this stage the absorption of other hon-complex salts formed takes place.
The different compounds are formed by selectivity of the processes that are achieved by applying electromagnetic wave frequency in the radio wave spectrum at 1 KHz to 2 MHz frequencies, by an electromagnetic wave generator having different geometry and frequency.
The possible fields of application for this technique, among others, are: o Seawater desalinization, chloride and sulphate precipitation. o Removal of salts from acid water from mining operations. o Precipitation of salts from mining PLS solutions. o Potable water treatment, precipitation of chlorides and sulphates. o Boiler water treatment and cooling, removal of sulphates and chlorides. o Irrigation water treatment, chloride and sulphate precipitation. o Irrigation water treatment, phosphate and nitrate precipitation. o Sewage treatment, precipitation of chlorides, sulphates and phosphates. o Sewage treatment, precipitation of nitrates and nitrites.
£400 8/7067 32 2879-2008 o Insolubilization of salts in processes for producing drugs and chemical reagents in general. o Precipitation of salts as pre-treatment for ultra-filtering and reverse osmosis processes.
Although these examples might be the ones most known, many other processes may make use of the advantages of being able to insolubilize regularly soluble salts and thus optimize the performance and/or purity of the products obtained. Accordingly, if a process were to use a part or the entire technology of the present invention, it would fall within the scope of the present invention.
This technology employs ultra-filtered continuous current, with a variable sinusoidal- type wave geometry, damped sawtooth pulse, square wave pulse, and an electromagnetic wave signal of the radio spectrum, which are applied through a couple of electrodes. All this, combined, is able to boost the precipitation reactions.
In addition, there must be a preferential pH range for said precipitation, which must be between pH 4 and pH 12. However, if the process is carried out at any of the ranges of the pH scale, good results will be obtained. Subsequently, there is an isokinetic coagulation stage of the precipitated particles, wherein this coagulation is electrically assisted. The voltage applied, corresponding to electric and magnetic fields, is also within a range, which must be between one and one hundred volts, whereas the current’s intensity employed must be between 10mA and 3A. As mentioned above, the voltage and the electromagnetic signal are applied through i ve 400 9 / ¢ 6 7 ik 2879-2008 electrodes that are submerged in the solution to be treated. The material used to construct said electrodes varies, depending on the quality of the water. These materials may be: lead, platinum, aluminum, copper, coal, gold, tin, zinc, iron, titanium, boron, nickel, or diamond.
The entire procedure to form insolubles is carried out in a single apparatus, which includes different elements, namely: - A reactor containing 1 pair of electrodes having a different configuration and made of a different material, inserted at a side of the reactor, one opposite the other, connected to a power supply and a magnetic induction source, which is outside of the apparatus. - A second pair of electrodes having a different configuration and made of a : different construction material, inserted within the reactor, one opposite the other and adjacent to the first pair of electrodes, connected to a frequency generator that is located outside of the reactor. - A spiral-shaped conducting element that is located outside of the reactor and connected to a power supply and a magnetic induction source, where, through this element flows current that generate specific magnetic fields. - Injection of photonized air produced by a blowing pump and a photon emitter that enters the reactor through a capillary located next to the electrode that is connected to the negative pole of the power supply, in order for the capillary to be as close as to the reactor’s bottom as possible.
B i : 2 0 0 g / 0 6 7 32 2879-2008 - An electric and magnetic field generator and an adjustable frequency generator located outside of the reactor. - A speed-adjustable paddle stirring means that is located at the center of the reactor.
In addition, the execution of all these processes may be carried out in other facilities with more than one apparatus.
The process of forming precipitates includes specific pressure and temperature values, which are within a range of 1 to 10 bars and 0 to 90°C ranges, respectively.
This is due to the fact that the precipitation process is based on the concentration, which implies a displacement of the balance constant, which allows oversaturation.
The effect of temperature affects the reaction’s kinetics, increasing the precipitation process, because molecular collisions accelerate and, as a result thereof, the kinetic constant rises. The application of external pressure leads to the same result. A clear example thereof is jarosite precipitation, which formation is not possible under normal conditions, for which reason the application of these variables is required.
Figure 1 shows the components of the invention and its connections therewith.
The process is carried out in a single step, in an apparatus including a reactor (1) having a pair of electrodes (2 and 3) connected to a power supply and a source
: rd 0 09 1067 32 2879-2008 magnetic induction (4), and a second pair of electrodes (5 and 6) connected to a frequency generator (7). A current of pressurized photonized air containing ozone and oxidant-free radicals enters the reactor from an air pump (9) that circulates air through a photon generator (10). Also, a spiral-shaped conducting element (11) surrounds the exterior of the reactor, through which circulates a current that generates specific magnetic fields. Said element is connected to a power supply and source of magnetic induction (4) that generates current. Everything is stirred with a mechanical or magnetic stirring device (8), and a chemical reagent adding the ions that are not present in the aqueous solution and that are necessary to complete the desired insoluble compounds is added. In most cases, the calcium and hydroxy! ions are insufficient, for which reason lime is preferably used as a single reagent.
The invention will now be described by way of the following non-limiting examples.
EXAMPLE 1:
If we take, for example, the application of the sea water desalinization process, the mechanism employed is as follows:
Firstly, an air mixture that passes through photons is applied, and then it is directly applied on the sea water. The resulting reactions are: 30s + H,0 ETE Hoge, THE Hon
The reaction above is applied until the pH > 9.8 units. The electric field is applied through aluminum electrodes causing a second electrolytic reaction that is:
} 2879-2008
A0eE52i78 4 36
The aluminum reacts with the OH ions forming the first nucleation based in the following reaction:
Pe
AIT 4 30H eZ (0H),
Once the aluminum hydroxide nuclei are formed, the calcium hydroxide is dosed and a 1.8MHz length wave radio frequency is applied, and then the following sulphate, chloride and phosphate precipitation reaction is formed: 60072 +3507 + 210K — ZT a A12(50.): (0H Ne 5 ATa™T 4+ 2007 + 2410H), + 35,04 20,0 EEE aC 5Ca~% + 30073 + OH es re (PO) OH fonic copper may be alternatively formed by applying, along with the formation of ionic aluminum, in a pair of copper electrodes to firstly form the reaction:
Cutlery? + 26 , The nitrate is captured from the medium based on the following reactions: 5
Cum 4 2807 SCu(VEL;
Cu™ + 0H sCu(0H),
With the above, and in the previous means of radio frequency and field, the following reaction is formed: 40051 4 2000 4 20H oC 000,), 3C (05);
The chlorides, sulphates, phosphates and nitrates have been precipitated. The removal of anions brings with it the removal of aluminum, copper and calcium. Each precipitate formed has a great capacity to absorb heavy metals.
- 2879-2008 ' o -
These insolubles as formed are generally micro-precipitates that must grow. In order to boost growth, flocculation is caused by adding a polymer and then by separating by settling and then by filtering.
The following chart shows the operational conditions and dosage at which the experience was carried out using sea water from San Antonio, 5th Region. 13 Total energy 31 Watts-h : 413 KW-h/m’®
The following chart shows the efficiencies reached when removing the salts from the seawater. The chart contains a raw column, which indicates the quality of seawater.
The treated column shows the value reached following sand and coal flocculation and filtering. The % removal column shows the validity obtained.
Element’ “Unit. Raw. Treated % Rémoval i 2879-2008
Example 2:
Another example of the application of salt precipitation is the insolubilization of sulphates in mining waters.
To this effect, a water sample, taken at Collahuasi Mine, with an initial content of 5,200 mg/L of sulphates.
The compound employed was precipitation, just as that of sodium jarosite.
MTAL(50:)- (0H)
The M element may be sodium or potassium. To this effect, the following mechanism was employed.
Firstly, an air mixture passing through photons is applied, and then it is directly applied on seawater. The resulting reactions are: 1 fp om BoRToREC 0 HzaEt 592 + Hy 00 ———20H %———204
The reaction above is applied until the pH > 9.8 units. The electric field is applied through aluminum electrodes causing a second electrolytic reaction that is: 500,505 4 36°
2879-2008
The aluminum reacts with the OH ions forming the first nucleation based in the following reaction:
AIF 4 BOH ead (OH),
In the balance aluminum hydroxide nuclei are formed, and then they precipitate as jarosite in the medium with radio frequency and electric field. = . REFaIc .
M+ 2410), +2507 + 4170S LAL (50.0: (0H) ]
The operational conditions are: 1 Aluminum 6 amperes
Intensity 9 Total energy 649 Watts-h 865 KW-vm’
The results obtained are:
Element” Unit Raw Treated ~% Removal
In this manner, different insoluble elements with which salts may be reduced may be configured.
Claims (14)
1. An apparatus for forming insoluble chemical compounds from salts contained in an aqueous solution to be treated, the apparatus including:- . a) A reactor including a pair of electrodes having a different configuration and made of a different material, inserted at a side of the reactor, one opposite the other, connected to a power supply and a magnetic induction source, which is outside of the apparatus; b) A second pair of electrodes having a different configuration and made of a different construction material, inserted within the reactor, one opposite the other and adjacent to the first pair of electrodes, connected to a frequency generator that is located outside of the reactor; ! c) A spiral-shaped conducting element that is located outside of the reactor and connected to a power supply and a magnetic induction source, where, through this element flows current that generate specific magnetic fields; d) A blowing pump and a photon emitter for producing photonized air and injecting it into the reactor through a capillary located next to the electrode that is connected to the negative pole of the power supply, in order for the capillary to be as close as to the reactor’s bottom as possible; e) An electric and magnetic field generator and an adjustable frequency generator, located outside of the reactor; and f) A speed-adjustable paddle stirring means that is located at the center of the reactor.
: 2879-2008
2. An apparatus as claimed in claim 1, wherein the power supply and the source \ of magnetic induction causes the application of an uitra-fitered continuous current voltage, with a variable sinusoidal-type wave geometry, damped sawtooth pulse, square wave pulse and an electromagnetic wave signal of the radio spectrum, which are applied through pairs of electrodes that, in combination or individually, are able to boost precipitation reactions, wherein these electrodes are contained in a device that connects them to electric and magnetic field generators and to frequency generators.
3. An apparatus as claimed in claim 1, wherein the reactions taking place within the reactor are within a whole range of the pH scale, preferably between pH 4 and pH 12, depending on the balance constant, followed by an electrically assisted kinetic coagulation stage of the precipitated particles.
4. An apparatus as claimed in claim 1, wherein the voltages applied correspond to electric and magnetic fields having a voltage between one and one hundred volts, and a current intensity between 10 mA and 3A.
5. An apparatus as claimed in claim 1, wherein the electric and magnetic fields and/or frequencies are transmitted through different kinds of pairs of electrodes that are made of one of the elements selected from the group including: lead, platinum, aluminum, copper, coal, gold, tin, zinc, iron, titanium, boron, nickel, diamond; this first electrode working in tandem with another electrode of the same element, with other electrodes manufactured from elements listed above or alloys thereof.
: 2879-2008 -2099/96138
6. An apparatus as claimed in claim 1, wherein the execution of all of the processes inside the reactor are within a temperature range between 0 and 90°C and within a pressure range between 1 and 10 bars.
7. A method for using an apparatus for forming insoluble chemical compounds including the steps of: a) providing a leaching reactor with a pair of electrodes having a different configuration and made of a different material, inserted at a side of the reactor, one opposite the other; b) providing a second pair of electrodes having a different configuration and made of a different construction material, inserted within the reactor, one opposite the other and adjacent to the first pair of electrodes; ¢) providing a power supply located outside of the reactor; d) providing a frequency generator located outside of the reactor; e) providing a photonized air injection system; f) providing an air pump and a capillary located adjacent to the electrode that is connected to the negative pole of the power supply; g) providing an electric and magnetic field generator and an adjustable frequency generator located outside of the reactor, h) providing a speed-adjustable paddle stirring means located at the center of the reactor; i) providing a spiral-shaped conducting element surrounding the outside of the reactor,
: 2879-2008 j) Introducing into the reactor a solution having insoluble chemical compounds; k) Injecting, by employing an air pump, the photonized air injector and the capillary, air containing ozone and free radicals into the reactor; ly Simultaneously, applying, by employing the frequency generator and a pair of electrodes, a frequency or a electromagnetic signal of the radio spectrum to a solution containing insoluble chemical compounds inside the reactor; m) Simultaneously, applying, by employing the power supply and another pair of electrodes, an electric voltage, consisting of pulsating continuous current, to the solution containing insoluble chemical compounds inside the reactor, n) Simultaneously, applying, by using the spiral-shaped conducting element, specific magnetic fields; 0) Simultaneously, stirring, by employing the paddle stirring means, the solution containing insoluble chemical compounds inside the reactor; p) Simultaneously, adding a chemical reagent adding ions that are not present in the aqueous solution and that are necessary to complete the desired insoluble compounds; and q) Adding a second contribution of ions to form new compounds with the salts contained in the aqueous solution.
8. A method as claimed in claim 7, wherein the chemical reagent of step p) is preferably lime.
9. A method as claimed in claim 7 or claim 8, wherein the ions added in step q) are selected from the group including: aluminum, calcium, iron, lead, and tin.
. 2879-2008
10.An apparatus for forming insoluble chemical compounds from salts contained in an aqueous solution to be treated according to the invention, as hereinbefore generally described.
11.An apparatus for forming insoluble chemical compounds from salts contained in an aqueous solution to be treated as specifically described with reference to or as illustrated in the accompanying drawing.
12.An apparatus for forming insoluble chemical compounds from salts contained in an aqueous solution to be treated including any new and inventive integer or combination of integers, substantially as herein described.
13.A method according to the invention for using an apparatus for forming insoluble chemical compounds, substantially as hereinbefore described or exemplified.
14.A method of using an apparatus for forming insoluble chemical compounds including any new and inventive integer or combination of integers, substantially as herein described. DATED AT PRETORIA THIS 28™ DAY OF SEPTEMBER 2009. : HAHN & HAHN INC. APPLICANT'S ATTORNEYS
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
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CL2008002879A CL2008002879A1 (en) | 2008-09-26 | 2008-09-26 | Device for the formation of insoluble chemical compounds in a liquid medium comprising a) a reactor containing a pair of electrodes and a second pair of electrodes, b) spiral-shaped conductor element, c) blower pump and photon emitter, d) generator of an electric / magnetic field, e) agitation medium; and method. |
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ZA200906732B true ZA200906732B (en) | 2010-06-30 |
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ZA200906732A ZA200906732B (en) | 2008-09-26 | 2009-09-28 | An apparatus for recovering soluble salts |
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US (1) | US20100078332A1 (en) |
JP (1) | JP2010115640A (en) |
CN (1) | CN101683605A (en) |
AR (1) | AR073321A1 (en) |
AU (1) | AU2009222427A1 (en) |
BR (1) | BRPI0903456A2 (en) |
CA (1) | CA2680991A1 (en) |
CL (1) | CL2008002879A1 (en) |
CO (1) | CO6210140A1 (en) |
DE (1) | DE102009043605A1 (en) |
FR (1) | FR2936508A1 (en) |
GB (1) | GB0916988D0 (en) |
IT (1) | IT1397168B1 (en) |
MX (1) | MX2009010359A (en) |
PE (1) | PE20100576A1 (en) |
SE (1) | SE0950705A2 (en) |
ZA (1) | ZA200906732B (en) |
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CL2011002879A1 (en) * | 2011-11-16 | 2012-06-22 | Quantum Matrix S P A | Process and system for the reduction of anions and cations in a liquid medium, which comprises passing ambient air through a first field of electromagnetic radiation (em), subjecting an oxidation column reactor to a second radiation field em, and subjecting a reactor with agitation to a third radiation field em. |
CN106555583B (en) * | 2016-11-14 | 2019-07-23 | 中国科学院力学研究所 | A kind of coal bed gas well ground coal powder output and flowing bottomhole pressure (FBHP) monitoring device and method |
CN108622987A (en) * | 2017-03-17 | 2018-10-09 | 周金华 | The device and method of photon vibration frequency and tinyization magnetic fluid character in a kind of stable water |
US10692619B2 (en) * | 2018-01-03 | 2020-06-23 | Reverse Ionizer Systems, Llc | Methods and devices for treating radionuclides in a liquid |
CN108128856B (en) * | 2018-02-05 | 2019-06-04 | 中国矿业大学 | Utilize the system of principle of electrophoresis control goaf filling weight metal transport |
CN108854798A (en) * | 2018-09-03 | 2018-11-23 | 上海卉沛生物科技有限公司 | A kind of radio frequency emulsifying device used for cosmetic |
EP3897905B1 (en) | 2018-11-21 | 2024-03-27 | Cameron Technologies Limited | Power unit phase angle for separation unit control |
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US5858249A (en) | 1997-02-21 | 1999-01-12 | Higby; Loren P. | Electrochemical insolubilization of anionic arsenic method and apparatus |
JP2004255627A (en) | 2003-02-25 | 2004-09-16 | Toppan Printing Co Ltd | Printed matter |
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- 2009-09-25 MX MX2009010359A patent/MX2009010359A/en not_active Application Discontinuation
- 2009-09-25 CO CO09104978A patent/CO6210140A1/en not_active Application Discontinuation
- 2009-09-27 CN CN200910178816A patent/CN101683605A/en active Pending
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CN101683605A (en) | 2010-03-31 |
IT1397168B1 (en) | 2013-01-04 |
PE20100576A1 (en) | 2010-09-16 |
CL2008002879A1 (en) | 2009-05-15 |
MX2009010359A (en) | 2010-08-17 |
AU2009222427A1 (en) | 2010-04-15 |
DE102009043605A1 (en) | 2010-04-01 |
GB0916988D0 (en) | 2009-11-11 |
JP2010115640A (en) | 2010-05-27 |
SE0950705A1 (en) | 2010-03-27 |
FR2936508A1 (en) | 2010-04-02 |
AR073321A1 (en) | 2010-10-28 |
CO6210140A1 (en) | 2010-10-20 |
ITMI20091661A1 (en) | 2010-03-27 |
US20100078332A1 (en) | 2010-04-01 |
CA2680991A1 (en) | 2010-03-26 |
SE0950705A2 (en) | 2010-07-20 |
BRPI0903456A2 (en) | 2011-06-14 |
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