WO2020102542A1 - Waste water fluoride and cyanide removal - Google Patents

Waste water fluoride and cyanide removal Download PDF

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Publication number
WO2020102542A1
WO2020102542A1 PCT/US2019/061490 US2019061490W WO2020102542A1 WO 2020102542 A1 WO2020102542 A1 WO 2020102542A1 US 2019061490 W US2019061490 W US 2019061490W WO 2020102542 A1 WO2020102542 A1 WO 2020102542A1
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ppm
water
rare earth
fluoride
cyanide
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PCT/US2019/061490
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French (fr)
Inventor
Vincent G. Spaeth
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Chemtreat, Inc.
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Publication of WO2020102542A1 publication Critical patent/WO2020102542A1/en

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    • CCHEMISTRY; METALLURGY
    • C02TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
    • C02FTREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
    • C02F1/00Treatment of water, waste water, or sewage
    • C02F1/52Treatment of water, waste water, or sewage by flocculation or precipitation of suspended impurities
    • C02F1/5236Treatment of water, waste water, or sewage by flocculation or precipitation of suspended impurities using inorganic agents
    • C02F1/5245Treatment of water, waste water, or sewage by flocculation or precipitation of suspended impurities using inorganic agents using basic salts, e.g. of aluminium and iron
    • CCHEMISTRY; METALLURGY
    • C02TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
    • C02FTREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
    • C02F1/00Treatment of water, waste water, or sewage
    • C02F1/52Treatment of water, waste water, or sewage by flocculation or precipitation of suspended impurities
    • C02F1/5209Regulation methods for flocculation or precipitation
    • CCHEMISTRY; METALLURGY
    • C02TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
    • C02FTREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
    • C02F1/00Treatment of water, waste water, or sewage
    • C02F1/52Treatment of water, waste water, or sewage by flocculation or precipitation of suspended impurities
    • C02F1/5236Treatment of water, waste water, or sewage by flocculation or precipitation of suspended impurities using inorganic agents
    • CCHEMISTRY; METALLURGY
    • C02TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
    • C02FTREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
    • C02F2101/00Nature of the contaminant
    • C02F2101/10Inorganic compounds
    • C02F2101/12Halogens or halogen-containing compounds
    • C02F2101/14Fluorine or fluorine-containing compounds
    • CCHEMISTRY; METALLURGY
    • C02TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
    • C02FTREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
    • C02F2101/00Nature of the contaminant
    • C02F2101/30Organic compounds
    • C02F2101/38Organic compounds containing nitrogen
    • CCHEMISTRY; METALLURGY
    • C02TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
    • C02FTREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
    • C02F2103/00Nature of the water, waste water, sewage or sludge to be treated
    • C02F2103/34Nature of the water, waste water, sewage or sludge to be treated from industrial activities not provided for in groups C02F2103/12 - C02F2103/32
    • CCHEMISTRY; METALLURGY
    • C02TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
    • C02FTREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
    • C02F2209/00Controlling or monitoring parameters in water treatment
    • C02F2209/06Controlling or monitoring parameters in water treatment pH
    • CCHEMISTRY; METALLURGY
    • C02TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
    • C02FTREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
    • C02F2209/00Controlling or monitoring parameters in water treatment
    • C02F2209/07Alkalinity

Definitions

  • coagulants include ferrous sulfate, ferrous chloride, ferric sulfate, ferric chloride, Potassium Aluminum Sulfate (Alum), Aluminum chloride, Aluminum Sulfate, Polyaluminum Chloride, and Aluminum Chlorohydrate, Sodium Aluminate, Calcium chloride, Magnesium Hydroxide, Magnesium Chloride, Lime, Bentonite Clay, Modified Starches, Tannins and Lignins. It is common to use slurries of insoluble inorganic coagulants or solutions of soluble coagulants to remove total dissolved solids (TDS) and total suspended solids (TSS), which include dissolved target elements for removal.
  • TDS total dissolved solids
  • TDS total suspended solids
  • Alkalinity may be added to waste streams in order to help biological processes such as nitrification/denitrification.
  • Coagulants such as ferrous, ferric and aluminum consume and are consumed by, alkalinity which can affect nitrification processes and creates additional demand for the product. In contrast, cerium is not affected by alkalinity.
  • waste fluid streams such as waste water form coke plants
  • coagulants and pH adjustment additives such as Fe2+/Fe3+/A12+ and caustic respectively, which are used to remove cyanide and fluoride.
  • this disclosure provides a method of treating waste water containing a concentration of fluoride and cyanide to reduce the concentration of fluoride and cyanide.
  • the method includes adding to the water at least one rare earth metal salt and at least one coagulant; and then reducing the concentration of fluoride and cyanide in the waste water.
  • this disclosure is directed to the unexpected discovery of a rare earth metal salt, such as CeC13, which demonstrates a synergy with other coagulants (such as iron salts and aluminum salts) in removing both cyanide and fluoride. This removal can be accomplished in combined or series precipitation steps. Overall pH control additive usage can be minimized since co-precipitation or series precipitation can be accomplished in similar pH control ranges (such as 5-7) and due to the lower total demand for coagulant additives. Although the examples described herein use cerium salt (CeC13), it would be expected that other rare earth metal salts such as lanthanum salts would show similar synergy with other coagulants.
  • Treating systems with a rare earth and another coagulant has an enhanced effect when parameters are controlled, such as pH or alkalinity.
  • This synergy can be taken advantage of to decrease chemical treatment costs or to optimize treatment.
  • Some advantages include: decrease in chemical consumption, decrease in overall sludge generation, decrease in corrosion of equipment, prevention of interference with biological processes and decreased consumption of alkalinity.
  • this disclosure thus employs a combination of a rare earth metal salts and/or aluminum salts and iron salts in coagulant applications for removing cyanide and/or fluoride.
  • Coagulants are used, for example, in water treatment applications to remove analytes from water streams, e.g., waste water streams.
  • metal salts and other coagulating agents are typically used in water treatment to effect a charge disruption that neutralizes repulsive forces in particles, which causes the particles or analyte to aggregate or floe, which enables them to be removed by filtration, clarification or other means.
  • At least one rare earth metal salt can be combined with any other coagulants, including one or more of ferrous sulfate, ferrous chloride, ferric sulfate, ferric chloride, Potassium Aluminum Sulfate (Alum), Aluminum chloride, Aluminum Sulfate, Polyaluminum Chloride, and Aluminum Chlorohydrate, Sodium Aluminate, Calcium chloride, Magnesium Hydroxide, Magnesium Chloride, and Lime.
  • the at least one rare earth metal salt can include, for example, cerium and lanthanum salts.
  • the treatment can be accomplished by adding the iron salts together with the rare earth metal salts and/or aluminum salts to a water stream that is allowed to accumulate in a tank, pond, or other holding area.
  • the rare earth and coagulant can be added to the water separately or together as a blend or in a series of coagulating steps.
  • the water can then be mechanically stirred or mixed to allow the target analyte of interest (e.g., phosphate, fluoride and/or cyanide) to aggregate.
  • the aggregate can then be separated from the water, e.g., by filtration or clarification, which will remove the analyte from the water.
  • Multiple tanks or holding ponds e.g., 2 to 10) can be arranged in series to improve the removal.
  • the time period to achieve effective aggregation that can be removed may be in the range of 10 minutes to 4 hours, 20 minutes to 2 hours, and 30 minutes to 1 hour.
  • the rare earth metal salt shows a synergy with coagulants so that the combination is more effective at removing cyanide and fluoride than would be expected based on the performance of each separately.
  • the optimum ratio depends on the target analyte being removed, and the pH or alkalinity.
  • the rare earth metal salt can be added in a weight ratio to total coagulant additives, i.e., on a dry basis, rare earth salt/(rare earth salt + other coagulants), that is in the range of 0.05-0.95, from 0.1-0.9, from 0.3-0.7, or from 0.4-0.6.
  • cyanide or fluoride may be present in the water in amounts in the range of from 1 ppm to 1,000 ppm, from 2-10 ppm, from 30 to 200 ppm, and from 50 to 100 ppm.
  • the combination of (i) the dosage of the rare earth and coagulant, and (ii) the pH and/or alkalinity are selected or controlled such that at least 50 wt.% of the target analyte is removed from the water, and preferably at least 75 wt.%, at least 90wt.%, at least 95 wt. %, and at least 99 wt. %.
  • the analyte can be present in amounts of less than 20 ppm, less than 10 ppm, less than 6 ppm, or from 10 ppb to 3 ppm.
  • the total dosage of rare earth and coagulant can be, on a dry basis, in the range of, for example, from 20 ppm to 4,000 ppm in the water, from 100 ppm to less than 1,500 ppm, from 150 ppm to less than 1,000 ppm, and from 200 ppm to less than 750 ppm.
  • the total dosage of rare earth, on a dry basis can be in a range of from 10 ppm to 2,500 ppm, from 20 ppm to 1,000 ppm, from 50 ppm to 750 ppm, and from 100 ppm to 500 ppm.
  • a ratio of the total dosage of rare earth and coagulant to the amount of fluoride in the water before treatment may be from 5 to 30, 10 to 30, less than 25, or less than 20.
  • an aluminum salt or an iron salt is used as the coagulant, it can be present in an amount of, on a dry basis, from 20 ppm to 2000 ppm, from 100 ppm to 400 ppm, or from 200 ppm to 300 ppm. As indicated above, using less of these types of salts can decrease sludge and sludge removal efforts. In some aspects, the amount of aluminum salt that is added can be less than 1,000 ppm, less than 500 ppm, or less than 250 ppm.
  • the rare earth metal salt and coagulants can be added as a solid salt form, or preferably as an aqueous solution.
  • the aqueous solution can include rare earth and/or coagulant in a total amount in the range of 10 to 70 weight percent, from 20 to 60 weight percent, or from 30 to 45 weight percent, where the balance is primarily water.
  • the aqueous solution can include from 2 wt. %-25 wt. % rare earth metal salt and from 2 wt. %-25 wt. % of coagulant, from 5 wt. %-20 wt. % of the rare earth metal salt and from 5 wt. %-20 wt.
  • the target analyte for coke plant waste water is generally fluoride and/or cyanide and can be removed by the rare earth/coagulant combination.
  • Another example would be the addition of iron salts and rare earth metal salts together (or in series) to remove multiple analytes (e.g. cyanide and fluoride) in the same or close pH control range
  • the synergy of the rare earth metal salt and coagulant depend on the pH and/or alkalinity of the water, these properties can be measured or controlled to optimize the synergy.
  • the particular optimum value can depend on the target analyte, the dosage, and the coagulant(s).
  • the pH can be measured (e.g., with a pH meter, pH paper, titration, etc.) and controlled so that the water is maintained within a target pH range (e.g., by adding caustic or an acid).
  • the amount of caustic that is added to the water can be less than 250 ppm, less than 200 ppm, or less than 150 ppm, for example.
  • the target pH range may be between 5 and 7, between 5 and 6.5, between 7.5 and 8, between 4.5 and 6.5, between 6 and 8, or between 4.5 and 5.5.
  • Alkalinity can similarly be measured (e.g., dye indicators, titration, etc.) and controlled to be within an optimal range (e.g., by adding buffer).
  • the control system can be automated by including on-line pH or alkalinity monitors that send measurement information to a computer, processor, or other controller, which in turn, communicates with pumps and/or valves that add acid, base, or buffer to keep the water within the target range.
  • the ratio and dosage of the rare earth/coagulant combination can be selected to be optimal for those properties.
  • the ratio and dosage can be determined based on empirically determined efficacies for removing the target analyte at varying pH levels and/or alkalinity levels.
  • cyanide and fluoride removal is normally accomplished in separate precipitation/clarification (using iron and aluminum salts respectively) steps due the pH requirement needed to drive each reaction.
  • rare earth metal salts are used (possibly in combination with aluminum salts) along with iron salts, co-precipitation or series precipitation process can be accomplished.
  • the target pH range may be between 5 and 7, between 5 and 6.5, between 7.5 and 8, between 4.5 and 6.5, between 6 and 8, or between 4.5 and 5.5.
  • Removal of cyanide from 1-100 ppm to ⁇ 1 ppm and removal of fluoride from 10-200 ppm to ⁇ 10 ppm can be accomplished with minimum pH control additives.
  • Table 1 summarizes the chemicals required to individually remove cyanide or fluoride and to also remove them together in a combined treatment or series treatment. Effective removal of fluoride can be accomplished with aluminum salts, P8200L or combinations thereof. Effective removal of cyanide can be accomplished with iron salts. However, the most effective treatment is the co-removal of both cyanide and fluoride in a combined precipitation or series addition process controlled in a similar close pH range that minimizes pH adjustment chemical usage/cost.

Abstract

A method for treating water to remove cyanide and/or fluoride that includes adding to the water a rare earth metal salt and an iron salt coagulant, and then removing cyanide and/or fluoride from the water. The treatment composition can be added as a blend that includes the coagulant and the rare earth metal salt.

Description

WASTE WATER FLUORIDE AND CYANIDE REMOVAL
BACKGROUND
Regulatory agencies place discharge limits on pollutants such as fluoride and cyanide. Facilities have used commodity coagulants to remove these contaminants with mixed results. Some common coagulants include ferrous sulfate, ferrous chloride, ferric sulfate, ferric chloride, Potassium Aluminum Sulfate (Alum), Aluminum chloride, Aluminum Sulfate, Polyaluminum Chloride, and Aluminum Chlorohydrate, Sodium Aluminate, Calcium chloride, Magnesium Hydroxide, Magnesium Chloride, Lime, Bentonite Clay, Modified Starches, Tannins and Lignins. It is common to use slurries of insoluble inorganic coagulants or solutions of soluble coagulants to remove total dissolved solids (TDS) and total suspended solids (TSS), which include dissolved target elements for removal.
In almost all cases, an excess of coagulant must be used to remove target elements. For example, to remove 50 ppm of fluoride it can take 1500-2000 ppm of alum at a pH of 6.6-8 to reduce fluoride to < 10 ppm. Also, to remove 10-20 ppm of total cyanide, it can take 500-1500 ppm of ferrous or ferric sulfate in pH ranges of 6-8 and 4.5-7.0 respectively. As chemical demand increases, pH control supplements also increase due to the acid content of the coagulants.
Excess coagulant feed results in higher chemical costs and generates excess sludge, which must be disposed of. Sometimes this excess sludge must be disposed of as hazardous waste. Additionally, some inorganic coagulants create sludge that is hard to dewater, further increasing disposal costs. Sludge containing Ce is typically compact while sludge containing A1 tends to hold more water. Aluminum coagulants can also adversely affect the microbial population in activated sludge, especially protozoa and rotifers. Some coagulants, such as FeC13 can cause corrosion to equipment.
Alkalinity may be added to waste streams in order to help biological processes such as nitrification/denitrification. Coagulants such as ferrous, ferric and aluminum consume and are consumed by, alkalinity which can affect nitrification processes and creates additional demand for the product. In contrast, cerium is not affected by alkalinity. SUMMARY
In treating waste fluid streams, such as waste water form coke plants, it would be advantageous to decrease the amount of coagulants and pH adjustment additives, such as Fe2+/Fe3+/A12+ and caustic respectively, which are used to remove cyanide and fluoride.
In one aspect, this disclosure provides a method of treating waste water containing a concentration of fluoride and cyanide to reduce the concentration of fluoride and cyanide. The method includes adding to the water at least one rare earth metal salt and at least one coagulant; and then reducing the concentration of fluoride and cyanide in the waste water.
DETAILED DESCRIPTION OF EMBODIMENTS
In one aspect, this disclosure is directed to the unexpected discovery of a rare earth metal salt, such as CeC13, which demonstrates a synergy with other coagulants (such as iron salts and aluminum salts) in removing both cyanide and fluoride. This removal can be accomplished in combined or series precipitation steps. Overall pH control additive usage can be minimized since co-precipitation or series precipitation can be accomplished in similar pH control ranges (such as 5-7) and due to the lower total demand for coagulant additives. Although the examples described herein use cerium salt (CeC13), it would be expected that other rare earth metal salts such as lanthanum salts would show similar synergy with other coagulants.
Treating systems with a rare earth and another coagulant has an enhanced effect when parameters are controlled, such as pH or alkalinity. This synergy can be taken advantage of to decrease chemical treatment costs or to optimize treatment. Some advantages include: decrease in chemical consumption, decrease in overall sludge generation, decrease in corrosion of equipment, prevention of interference with biological processes and decreased consumption of alkalinity.
It has further been discovered that at various pHs and/or alkalinities there is a synergy that allows for treatment of wastewater that costs significantly less by using coagulant/rare earth in combination, when compared to either rare earth salts or inorganic coagulant alone. While rare earth salts have been used to remove TSS and TDS in wastewater, they are expensive and thus their cost to treat is expensive as well.
In one aspect, this disclosure thus employs a combination of a rare earth metal salts and/or aluminum salts and iron salts in coagulant applications for removing cyanide and/or fluoride. Coagulants are used, for example, in water treatment applications to remove analytes from water streams, e.g., waste water streams. In this regard, metal salts and other coagulating agents are typically used in water treatment to effect a charge disruption that neutralizes repulsive forces in particles, which causes the particles or analyte to aggregate or floe, which enables them to be removed by filtration, clarification or other means.
In accordance with this disclosure, at least one rare earth metal salt can be combined with any other coagulants, including one or more of ferrous sulfate, ferrous chloride, ferric sulfate, ferric chloride, Potassium Aluminum Sulfate (Alum), Aluminum chloride, Aluminum Sulfate, Polyaluminum Chloride, and Aluminum Chlorohydrate, Sodium Aluminate, Calcium chloride, Magnesium Hydroxide, Magnesium Chloride, and Lime. The at least one rare earth metal salt can include, for example, cerium and lanthanum salts.
The treatment can be accomplished by adding the iron salts together with the rare earth metal salts and/or aluminum salts to a water stream that is allowed to accumulate in a tank, pond, or other holding area. The rare earth and coagulant can be added to the water separately or together as a blend or in a series of coagulating steps. The water can then be mechanically stirred or mixed to allow the target analyte of interest (e.g., phosphate, fluoride and/or cyanide) to aggregate. The aggregate can then be separated from the water, e.g., by filtration or clarification, which will remove the analyte from the water. Multiple tanks or holding ponds (e.g., 2 to 10) can be arranged in series to improve the removal. The time period to achieve effective aggregation that can be removed may be in the range of 10 minutes to 4 hours, 20 minutes to 2 hours, and 30 minutes to 1 hour.
As indicated above, the rare earth metal salt shows a synergy with coagulants so that the combination is more effective at removing cyanide and fluoride than would be expected based on the performance of each separately. As demonstrated in the Examples below, the optimum ratio depends on the target analyte being removed, and the pH or alkalinity. The rare earth metal salt can be added in a weight ratio to total coagulant additives, i.e., on a dry basis, rare earth salt/(rare earth salt + other coagulants), that is in the range of 0.05-0.95, from 0.1-0.9, from 0.3-0.7, or from 0.4-0.6.
Before treatment, cyanide or fluoride may be present in the water in amounts in the range of from 1 ppm to 1,000 ppm, from 2-10 ppm, from 30 to 200 ppm, and from 50 to 100 ppm. Preferably, the combination of (i) the dosage of the rare earth and coagulant, and (ii) the pH and/or alkalinity, are selected or controlled such that at least 50 wt.% of the target analyte is removed from the water, and preferably at least 75 wt.%, at least 90wt.%, at least 95 wt. %, and at least 99 wt. %. After treatment, the analyte can be present in amounts of less than 20 ppm, less than 10 ppm, less than 6 ppm, or from 10 ppb to 3 ppm.
The total dosage of rare earth and coagulant can be, on a dry basis, in the range of, for example, from 20 ppm to 4,000 ppm in the water, from 100 ppm to less than 1,500 ppm, from 150 ppm to less than 1,000 ppm, and from 200 ppm to less than 750 ppm. The total dosage of rare earth, on a dry basis, can be in a range of from 10 ppm to 2,500 ppm, from 20 ppm to 1,000 ppm, from 50 ppm to 750 ppm, and from 100 ppm to 500 ppm. A ratio of the total dosage of rare earth and coagulant to the amount of fluoride in the water before treatment may be from 5 to 30, 10 to 30, less than 25, or less than 20.
Where an aluminum salt or an iron salt is used as the coagulant, it can be present in an amount of, on a dry basis, from 20 ppm to 2000 ppm, from 100 ppm to 400 ppm, or from 200 ppm to 300 ppm. As indicated above, using less of these types of salts can decrease sludge and sludge removal efforts. In some aspects, the amount of aluminum salt that is added can be less than 1,000 ppm, less than 500 ppm, or less than 250 ppm.
Whether added separately or as a blend, the rare earth metal salt and coagulants can be added as a solid salt form, or preferably as an aqueous solution. The aqueous solution can include rare earth and/or coagulant in a total amount in the range of 10 to 70 weight percent, from 20 to 60 weight percent, or from 30 to 45 weight percent, where the balance is primarily water. Thus, in some aspects, the aqueous solution can include from 2 wt. %-25 wt. % rare earth metal salt and from 2 wt. %-25 wt. % of coagulant, from 5 wt. %-20 wt. % of the rare earth metal salt and from 5 wt. %-20 wt. % of the coagulant, or from 5 wt. %-15 wt. % of the rare earth metal salt and from 15 wt. %-25 wt. % of the coagulant. Typically, the rare earth metal salt will be present in a lower amount than the coagulant. The target analyte for coke plant waste water is generally fluoride and/or cyanide and can be removed by the rare earth/coagulant combination. Another example would be the addition of iron salts and rare earth metal salts together (or in series) to remove multiple analytes (e.g. cyanide and fluoride) in the same or close pH control range
In one aspect, because the synergy of the rare earth metal salt and coagulant depend on the pH and/or alkalinity of the water, these properties can be measured or controlled to optimize the synergy. Here also, and as demonstrated by the Examples below, the particular optimum value can depend on the target analyte, the dosage, and the coagulant(s). In general, the pH can be measured (e.g., with a pH meter, pH paper, titration, etc.) and controlled so that the water is maintained within a target pH range (e.g., by adding caustic or an acid). The amount of caustic that is added to the water can be less than 250 ppm, less than 200 ppm, or less than 150 ppm, for example. Depending on the factors indicated above, the target pH range may be between 5 and 7, between 5 and 6.5, between 7.5 and 8, between 4.5 and 6.5, between 6 and 8, or between 4.5 and 5.5. Alkalinity can similarly be measured (e.g., dye indicators, titration, etc.) and controlled to be within an optimal range (e.g., by adding buffer). The control system can be automated by including on-line pH or alkalinity monitors that send measurement information to a computer, processor, or other controller, which in turn, communicates with pumps and/or valves that add acid, base, or buffer to keep the water within the target range.
In another aspect, e.g., where it may not be feasible to readily alter the pH or alkalinity of the water, the ratio and dosage of the rare earth/coagulant combination can be selected to be optimal for those properties. The ratio and dosage can be determined based on empirically determined efficacies for removing the target analyte at varying pH levels and/or alkalinity levels.
EXAMPLES
In prior methods, cyanide and fluoride removal is normally accomplished in separate precipitation/clarification (using iron and aluminum salts respectively) steps due the pH requirement needed to drive each reaction. However, when rare earth metal salts are used (possibly in combination with aluminum salts) along with iron salts, co-precipitation or series precipitation process can be accomplished. Depending on the factors indicated above, the target pH range may be between 5 and 7, between 5 and 6.5, between 7.5 and 8, between 4.5 and 6.5, between 6 and 8, or between 4.5 and 5.5. Removal of cyanide from 1-100 ppm to < 1 ppm and removal of fluoride from 10-200 ppm to < 10 ppm can be accomplished with minimum pH control additives.
Table 1
Cyanide and Fluoride Removal
Figure imgf000007_0001
Data summarized in Table 1 summarizes the chemicals required to individually remove cyanide or fluoride and to also remove them together in a combined treatment or series treatment. Effective removal of fluoride can be accomplished with aluminum salts, P8200L or combinations thereof. Effective removal of cyanide can be accomplished with iron salts. However, the most effective treatment is the co-removal of both cyanide and fluoride in a combined precipitation or series addition process controlled in a similar close pH range that minimizes pH adjustment chemical usage/cost.

Claims

WHAT IS CLAIMED IS
1. A method of treating waste water containing a concentration of fluoride and cyanide to reduce the concentration of fluoride and cyanide, the method comprising:
adding to the water at least one rare earth metal salt and at least one coagulant; and
then reducing the concentration of fluoride and cyanide in the waste water.
2. The method according to claim 1, wherein an amount of the rare earth metal salt and the coagulant are added, so that at least 50 wt.% of the fluoride and/or cyanide is removed from the water.
3. The method according to claim 2, wherein the total amount, on a dry basis, of the rare earth metal salt and the coagulants added to the water is in the range of 50 ppm to 4,000 ppm (wt./wt.).
4. The method according to claim 1, further including adjusting the pH and/or alkalinity to be within a target range by adding to the water at least one of an acid, a base, and a buffer.
5. The method according to claim 4, wherein the amount of the at least one acid, base, and buffer is added based on the determined pH.
6. The method according to claim 1, wherein the at least one rare earth metal salt and the at least one coagulant are added to the water as a blend.
7. The method according to claim 1, including a step of controlling the pH to be within the range of 5-7.5
8. The method according claim 1, further including a step of determining the target range based on a synergistic high point, for maximum-efficiency removal of the target analyte, of pH values and relative amounts of the rare earth metal salt and coagulants.
9. The method according to claim 1, wherein the rare earth metal salt comprises CeC13.
10. The method according to claim 1, wherein the coagulant comprises an iron salt.
11. The method according to claim 1, wherein the waste water is waste water from a coke plant.
12. The method according to claim 1, wherein, prior to the treatment, the waste water includes a concentration of cyanide that is in a range of from 1 ppm to 1,000 ppm (wt./wt.), and includes a concentration of fluoride that is in a range of from 1 ppm to 1,000 ppm (wt./wt.)·
13. The method according to claim 12, wherein, prior to the treatment, the waste water includes a concentration of fluoride that is in a range of from 30 ppm to 200 ppm (wt./wt.).
14. The method according to claim 10, wherein an amount of caustic that is added to the water is less than 250 ppm (wt./wt.).
15. The method according to claim 14, including a step of controlling the pH to be within a range of from 5.5 and 6.5.
16. The method according to claim 1, wherein the step of reducing the
concentration of fluoride and cyanide in the waste water comprises removing aggregated or flocculated particles that include the fluoride and cyanide from the water.
17. The method according to claim 16, wherein the aggregated or flocculated particles are removed by a filtration or clarification process.
18. The method according to claim 1, wherein an amount of aluminum salt that is added to the water is less than 1,000 ppm (wt./wt.).
19. The method according to claim 1, wherein the total amount, on a dry basis, of the rare earth metal salt added to the water is in the range of 10 ppm to 2,500 ppm (wt./wt.).
20. The method according to claim 1, wherein the total amount, on a dry basis, of the rare earth metal salt added to the water is in the range of 50 ppm to 750 ppm (wt./wt.).
PCT/US2019/061490 2018-11-14 2019-11-14 Waste water fluoride and cyanide removal WO2020102542A1 (en)

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* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN111995020A (en) * 2020-08-26 2020-11-27 常熟理工学院 Preparation method of polymeric magnesium aluminum cerium chloride coagulant
CN112850867A (en) * 2021-01-22 2021-05-28 北京华德创业环保设备有限公司 Deep defluorination medicament and preparation method thereof
CN113788568A (en) * 2021-10-14 2021-12-14 上海宝汇环境科技有限公司 Coking wastewater advanced treatment and coupling fluoride ion removal process

Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20100150818A1 (en) * 1997-09-16 2010-06-17 Clearvalue Technologies, Inc. Clarification of water and wastewater
CN103991947A (en) * 2014-05-16 2014-08-20 上海纳米技术及应用国家工程研究中心有限公司 Method for ozonizing coking wastewater by using modified molecular sieve as catalyst
CN105967295A (en) * 2016-06-27 2016-09-28 安徽世绿环保科技有限公司 Electroplating wastewater synchronous dephosphorization-defluorination compound flocculant and preparation method thereof
KR20180114325A (en) * 2017-04-10 2018-10-18 김상수 Waste water treatment method of removing fluorine and cyanides using rare metal

Patent Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20100150818A1 (en) * 1997-09-16 2010-06-17 Clearvalue Technologies, Inc. Clarification of water and wastewater
CN103991947A (en) * 2014-05-16 2014-08-20 上海纳米技术及应用国家工程研究中心有限公司 Method for ozonizing coking wastewater by using modified molecular sieve as catalyst
CN105967295A (en) * 2016-06-27 2016-09-28 安徽世绿环保科技有限公司 Electroplating wastewater synchronous dephosphorization-defluorination compound flocculant and preparation method thereof
KR20180114325A (en) * 2017-04-10 2018-10-18 김상수 Waste water treatment method of removing fluorine and cyanides using rare metal

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN111995020A (en) * 2020-08-26 2020-11-27 常熟理工学院 Preparation method of polymeric magnesium aluminum cerium chloride coagulant
CN112850867A (en) * 2021-01-22 2021-05-28 北京华德创业环保设备有限公司 Deep defluorination medicament and preparation method thereof
CN113788568A (en) * 2021-10-14 2021-12-14 上海宝汇环境科技有限公司 Coking wastewater advanced treatment and coupling fluoride ion removal process

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