USH1661H - Ion exchange removal of cations under chelating/complexing conditions - Google Patents

Ion exchange removal of cations under chelating/complexing conditions Download PDF

Info

Publication number
USH1661H
USH1661H US08/300,288 US30028894A USH1661H US H1661 H USH1661 H US H1661H US 30028894 A US30028894 A US 30028894A US H1661 H USH1661 H US H1661H
Authority
US
United States
Prior art keywords
cation
resin
anion
complex
cations
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Abandoned
Application number
US08/300,288
Inventor
Jennie L. Koff
Daniel A. Zarate
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
US Department of Navy
Original Assignee
US Department of Navy
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by US Department of Navy filed Critical US Department of Navy
Priority to US08/300,288 priority Critical patent/USH1661H/en
Assigned to UNITED STATES OF AMERICA, THE, AS REPRESENTED BY THE SECRETARY OF THE NAVY reassignment UNITED STATES OF AMERICA, THE, AS REPRESENTED BY THE SECRETARY OF THE NAVY ASSIGNMENT OF ASSIGNORS INTEREST (SEE DOCUMENT FOR DETAILS). Assignors: KOFF, JENNIE L., ZARATE, DANIEL A.
Application granted granted Critical
Publication of USH1661H publication Critical patent/USH1661H/en
Abandoned legal-status Critical Current

Links

Images

Classifications

    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J45/00Ion-exchange in which a complex or a chelate is formed; Use of material as complex or chelate forming ion-exchangers; Treatment of material for improving the complex or chelate forming ion-exchange properties

Definitions

  • the present invention relates to a process for removing complexed or chelated cations from an aqueous solution using a cationic ion exchange resin.
  • the invention relates to a process for removing heavy metal cations from a chelate or complex with cyanide and, more particularly, cadmium from a cadmium cyanide complex dissolved in the aqueous effluent of a plating bath such that the cadmium can be recycled or recovered for reuse and the cyanide is recycled or converted to a form which can be disposed of with minimal effect on the environment.
  • Electroplating baths are used to plate numerous different metals, such as cadmium, copper, zinc, silver, gold and nickel, on to a conductive substrate.
  • One of the major problems with the use of electroplating baths is the need to dispose of high volumes of metals complexed or chelated with cyanides (referred to below as the cyanide complex) which are generated in the process and are present in the waste streams.
  • the most common method of treating this waste stream is to react the cyanide complex with chlorine in the form of chlorine gas, sodium hypochlorite or calcium hypochlorite followed by the addition of an alkali, such as caustic soda, to raise the pH to 9 to 11 to convert the cyanide to cyanate and then to CO 2 and N 2 , releasing the metal ion from the complex in the process.
  • An alternative method is the use of ozone and hydrogen peroxide.
  • the solution is then treated with hydroxide to form an insoluble precipitate of the heavy metal, the resulting metal hydroxide sludge being disposed of as hazardous waste as it is not in a form which can be readily recovered, recycled or reused.
  • Ion exchange resins are polymeric materials which have charged functional groups exposed to the aqueous feed stream. The charge on the functional group determines the type of ions which can be attracted by the resin. For example, some cationic resins typically contain sulfonic acid groups which are negatively charged and thus attract positively charged cations. Some anionic resins contain amine-based functional groups which are positively charged and thus attract anionic groups.
  • anionic ion exchange resin can be used in place of alkaline chlorination to remove free cyanide as well as cyanide complexes such as Cd(CN) 4 -2 , Zn(CN) 4 -2 , Fe(CN) 4 -2 , or Fe(CN) 6 -4 .
  • these complexes are strongly bound to the anionic resin and not readily removed by standard NaOH resin regeneration treatment, resulting in rapid degeneration of the resin and a short useful processing life.
  • Cationic resins can be used to remove cations from solution after the complex is broken with subsequent release by acid treatment.
  • Rohm and Haas Company markets Amberlite® IRC-178 chelating resin for the removal of cations from aqueous solutions.
  • pH highly acidic solution
  • selectivity rapidly decreasing as the pH is raised to neutral or basic.
  • Other published material U.S. Pat. Nos.
  • U.S. Pat. No. 5,200,473 to Jeanneret-Gris suggests that a chelating resin may be used to draw a metal ion out of a weak complex.
  • complexes of metals with cyanide are extremely stable and known chelating resins can be unsuitable and undesirable when they produce toxic gases.
  • such resins can be regenerated by washing the resin with a basic pH solution of cyanide ions, reversing the attraction of the chelating resin for the metal, i.e., forming instead of breaking the cyanide/metal ion complex.
  • U.S. Pat. No. 5,198,021 discloses the use of a guanidine based resin specifically designed to recover gold or silver complexed with cyanide.
  • this resin which is a hydrogen form resin, suffers from at least two deficiencies--the exchange results in the formation of highly toxic HCN gas and regeneration of the resin, i.e., removal of the absorbed metal, is performed using NaOH which would produce heavy metal hydroxides from which the free metal is not readily recovered.
  • the present invention comprises the use of a chelating type cationic resin to directly treat an aqueous solution of a metal cyanide complex.
  • the process comprises passing a highly basic (pH ⁇ 8.5) aqueous stream of soluble, cyanide complexed metal solution over a chelating cationic resin in the sodium form preferentially including an iminodiacetic acid chelating agent which causes the removal of the metal ion from the cyanide complex, regenerating the resin by washing with a strong acid, such as hydrochloric or sulfuric acid, to form an acidic solution of the metal.
  • the metal ion can be recovered as elemental metal by passing the solution through an electrolytic bath where the metal is deposited on the cathode.
  • the cyanide can be removed using an anionic resin or destroyed by a standard chlorination processing.
  • the chelating resin can then be reactivated by treatment with a base such as NaOH.
  • FIG. 1 is a schematic drawing showing a process according to the invention.
  • a sodium type cationic resin will remove ions from an acidic solution, but that the resin will not exchange the sodium for the metal ion when it is complexed with cyanide.
  • a highly basic solution of a negatively charged, metal complex is passed over a cationic chelating type resin the metal is removed from the cyanide complex, resulting in the metal being bound by the chelating resin and the cyanide anion passing through the system.
  • the cationic resin can then be readily regenerated using sulfuric acid to produce a concentrated acidic solution of the metal ion and the metal recovered using standard processing techniques such as electrolytic deposition which converts the ion to elemental metal.
  • the cyanide ion passing through the system can be recovered using an anionic resin or decomposed using standard alkaline chlorination.
  • FIG. 1 illustrates schematically a particular version of the process for recovering free cadmium metal from a cadmium cyanide complex in water.
  • the system 10 includes three resin columns 12, 14, 16, each containing an iminodiacetate cation chelating material, such as Rohm and Haas Amberlite® IRC-718.
  • An aqueous solution containing a cyanide complex 11 is fed from a plating bath rinse tank 18 through a feed system 20 into first and second resin columns 12, 14 (a lead column and a polish column) placed in series until the first column (the lead column) is exhausted, as evidenced by heavy metal breakthrough (an increase in the heavy metal content of the feed stream) monitored between the lead and polish columns.
  • the first column is then taken off stream for regeneration, the second column becomes the lead column and the third column becomes the polish column. Once the first column is regenerated it becomes the backup column to the other two columns.
  • the depleted solution 22, substantially free of heavy metal ions but containing a dissolved cyanide salt, exiting the polish column is then fed to further processing vessels 24 for cyanide removal by an anionic resin, membrane separation or alkaline chlorination.
  • the exhausted column which now has a heavy concentration of heavy metal, such as cadmium, is washed with water to remove any residual cyanide and treated with 10% sulfuric acid fed from the acid tank 26 to remove the metal ion in the form of a soluble metal sulfate, such as CdSO 4 .
  • the resin is washed with water and converted to the sodium form by passing 5% NaOH fed from the hydroxide tank 28, therethrough.
  • FIG. 1 shows three resin columns and equipment for recovering or regenerating the effluent streams
  • one or two columns can be used and the process can be performed in a semi-continuous or batch mode.
  • the effluent streams containing anions or cations can be recovered, recycled, processed or collected for separate treatment or disposal.
  • other comparable regenerating solutions such as potassium hydroxide, may be used.
  • Typical design and operating conditions are listed in Tables 1 and 2. However, these conditions are given as examples and are not necessarily critical to the operation. In particular, the column sizes and flow rates are not critical to the invention.
  • the resin capacity for cadmium varied from 75 meq/L to 630 meq/L with the average capacity when RO water was used in place of city water for rinsing being about 480 meq/L.
  • metals can be removed from cyanide complexes in water using standard chelating cationic resins in an unconventional manner without resin degeneration or the potential of hydrogen cyanide gas formation and release.
  • heavy metals such as cadmium, are removed in a form suitable for recovery or recycling to the plating baths instead of disposal as toxic sludge.
  • the process set forth above for recovering cyanide complexed cadmium can be applied to the removal from a solvent system of any ion, such as a metal ion having a positive charge, complexed or chelated with a second ion of an opposite charge, such that the complex or chelate has a neutral charge or a charge opposite to that of the metal ion itself (i.e.
  • a complexed cation has a negative charge
  • a chelating resin with active sites on the resin chelate oppositely charged to the ion if unbound (i.e., the metal ion) and the same charge as the chelated ion.
  • negatively or neutrally charged chelates or complexes of various metals including, but not limited to, mercury, copper, gold, silver, lead, nickel, zinc, cobalt, iron, magnesium, cadmium and calcium can be removed from a basic (pH ⁇ 7.0), aqueous feed stream by passing the solution over a cationic chelating resin.

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Treatment Of Water By Ion Exchange (AREA)

Abstract

A process for removing complexed or chelated ions from an aqueous solution using a cationic chelating resin in the sodium form. The process is particularly useful for removing metal ions chelated during a metal plating process with specific utility for recovering cadmium from a cadmium cyanide complex.

Description

BACKGROUND
The present invention relates to a process for removing complexed or chelated cations from an aqueous solution using a cationic ion exchange resin. In particular, the invention relates to a process for removing heavy metal cations from a chelate or complex with cyanide and, more particularly, cadmium from a cadmium cyanide complex dissolved in the aqueous effluent of a plating bath such that the cadmium can be recycled or recovered for reuse and the cyanide is recycled or converted to a form which can be disposed of with minimal effect on the environment.
Electroplating baths are used to plate numerous different metals, such as cadmium, copper, zinc, silver, gold and nickel, on to a conductive substrate. One of the major problems with the use of electroplating baths is the need to dispose of high volumes of metals complexed or chelated with cyanides (referred to below as the cyanide complex) which are generated in the process and are present in the waste streams. The most common method of treating this waste stream is to react the cyanide complex with chlorine in the form of chlorine gas, sodium hypochlorite or calcium hypochlorite followed by the addition of an alkali, such as caustic soda, to raise the pH to 9 to 11 to convert the cyanide to cyanate and then to CO2 and N2, releasing the metal ion from the complex in the process. An alternative method is the use of ozone and hydrogen peroxide. The solution is then treated with hydroxide to form an insoluble precipitate of the heavy metal, the resulting metal hydroxide sludge being disposed of as hazardous waste as it is not in a form which can be readily recovered, recycled or reused.
An alternative recovery process involves the use of an ion exchange resin to remove certain ionic materials. Ion exchange resins are polymeric materials which have charged functional groups exposed to the aqueous feed stream. The charge on the functional group determines the type of ions which can be attracted by the resin. For example, some cationic resins typically contain sulfonic acid groups which are negatively charged and thus attract positively charged cations. Some anionic resins contain amine-based functional groups which are positively charged and thus attract anionic groups. Thus, anionic ion exchange resin can be used in place of alkaline chlorination to remove free cyanide as well as cyanide complexes such as Cd(CN)4 -2, Zn(CN)4 -2, Fe(CN)4 -2, or Fe(CN)6 -4. However, these complexes are strongly bound to the anionic resin and not readily removed by standard NaOH resin regeneration treatment, resulting in rapid degeneration of the resin and a short useful processing life.
Cationic resins can be used to remove cations from solution after the complex is broken with subsequent release by acid treatment. As an example, the Rohm and Haas Company markets Amberlite® IRC-178 chelating resin for the removal of cations from aqueous solutions. To obtain high selectivity the most effective operative conditions require the use of a highly acidic solution (pH=2.0), the selectivity rapidly decreasing as the pH is raised to neutral or basic. Other published material (U.S. Pat. Nos. 5,262,018 and 5,200,473) disclose that iminodiacetic acid resins produced by numerous other manufacturers, N-hydroxypropyloicolylamine functionalized chloromethylated polymer (Dowex® XFS-415 and XFS-43084) and chelating resins with amino phosphoric acid functional groups (Duolite® C-467) behave similarly for removing free ions of transition metals over the pH range of 0.5 to 4.0.
While strong acid cationic resins in the hydrogen form can be used to remove complexed heavy metals, strong acid cationic resins in the sodium form will not remove complexed heavy metals. However, when used on cyanide complexing solutions, the hydrogen form of cationic resins cause the cyanide complex to break down and release hydrogen cyanide gas which is highly toxic.
U.S. Pat. No. 5,200,473 to Jeanneret-Gris suggests that a chelating resin may be used to draw a metal ion out of a weak complex. However, complexes of metals with cyanide are extremely stable and known chelating resins can be unsuitable and undesirable when they produce toxic gases. In fact, such resins can be regenerated by washing the resin with a basic pH solution of cyanide ions, reversing the attraction of the chelating resin for the metal, i.e., forming instead of breaking the cyanide/metal ion complex.
U.S. Pat. No. 5,198,021 discloses the use of a guanidine based resin specifically designed to recover gold or silver complexed with cyanide. However, this resin, which is a hydrogen form resin, suffers from at least two deficiencies--the exchange results in the formation of highly toxic HCN gas and regeneration of the resin, i.e., removal of the absorbed metal, is performed using NaOH which would produce heavy metal hydroxides from which the free metal is not readily recovered.
Thus there is a need for a safe, economical, and reliable process which will allow the recovery of high volumes of heavy metals from wastewater streams in a form suitable for recovery or recycling while at the same time avoiding the production of hazardous waste and toxic gases.
SUMMARY
These needs are met by the present invention which comprises the use of a chelating type cationic resin to directly treat an aqueous solution of a metal cyanide complex. The process comprises passing a highly basic (pH≧8.5) aqueous stream of soluble, cyanide complexed metal solution over a chelating cationic resin in the sodium form preferentially including an iminodiacetic acid chelating agent which causes the removal of the metal ion from the cyanide complex, regenerating the resin by washing with a strong acid, such as hydrochloric or sulfuric acid, to form an acidic solution of the metal. The metal ion can be recovered as elemental metal by passing the solution through an electrolytic bath where the metal is deposited on the cathode. The cyanide can be removed using an anionic resin or destroyed by a standard chlorination processing. The chelating resin can then be reactivated by treatment with a base such as NaOH.
DRAWINGS
These and other features, aspects and advantages of the present invention will become better understood with reference to the following description, appended claims, and accompanying drawings, where:
FIG. 1 is a schematic drawing showing a process according to the invention.
DESCRIPTION
It is known that a sodium type cationic resin will remove ions from an acidic solution, but that the resin will not exchange the sodium for the metal ion when it is complexed with cyanide. Unexpectedly, it has been found that when a highly basic solution of a negatively charged, metal complex is passed over a cationic chelating type resin the metal is removed from the cyanide complex, resulting in the metal being bound by the chelating resin and the cyanide anion passing through the system. The cationic resin can then be readily regenerated using sulfuric acid to produce a concentrated acidic solution of the metal ion and the metal recovered using standard processing techniques such as electrolytic deposition which converts the ion to elemental metal. The cyanide ion passing through the system can be recovered using an anionic resin or decomposed using standard alkaline chlorination.
FIG. 1 illustrates schematically a particular version of the process for recovering free cadmium metal from a cadmium cyanide complex in water. In the illustrated configuration, the system 10 includes three resin columns 12, 14, 16, each containing an iminodiacetate cation chelating material, such as Rohm and Haas Amberlite® IRC-718. An aqueous solution containing a cyanide complex 11 is fed from a plating bath rinse tank 18 through a feed system 20 into first and second resin columns 12, 14 (a lead column and a polish column) placed in series until the first column (the lead column) is exhausted, as evidenced by heavy metal breakthrough (an increase in the heavy metal content of the feed stream) monitored between the lead and polish columns. The first column is then taken off stream for regeneration, the second column becomes the lead column and the third column becomes the polish column. Once the first column is regenerated it becomes the backup column to the other two columns. The depleted solution 22, substantially free of heavy metal ions but containing a dissolved cyanide salt, exiting the polish column is then fed to further processing vessels 24 for cyanide removal by an anionic resin, membrane separation or alkaline chlorination. The exhausted column, which now has a heavy concentration of heavy metal, such as cadmium, is washed with water to remove any residual cyanide and treated with 10% sulfuric acid fed from the acid tank 26 to remove the metal ion in the form of a soluble metal sulfate, such as CdSO4. Once depleted of its removable metal content, the resin is washed with water and converted to the sodium form by passing 5% NaOH fed from the hydroxide tank 28, therethrough.
While FIG. 1 shows three resin columns and equipment for recovering or regenerating the effluent streams one skilled in the art will recognize that one or two columns can be used and the process can be performed in a semi-continuous or batch mode. Also the effluent streams containing anions or cations can be recovered, recycled, processed or collected for separate treatment or disposal. Also, other comparable regenerating solutions, such as potassium hydroxide, may be used. Thus, it is not necessary that all of the processing steps shown in FIG. 1 be performed or that they be performed in a continuous mode.
Typical design and operating conditions are listed in Tables 1 and 2. However, these conditions are given as examples and are not necessarily critical to the operation. In particular, the column sizes and flow rates are not critical to the invention. Depending on the quantity of other cations (Ca, Mg, Na, etc) in the wash water (city water has significant quantities of dissolved alkali metals,) the resin capacity for cadmium varied from 75 meq/L to 630 meq/L with the average capacity when RO water was used in place of city water for rinsing being about 480 meq/L.
The cadmium recovery (actual Cd capacity), through put until full column saturation (complete breakthrough) and through put until regulatory limits are reached in the outflow (Regulatory Breakthrough) in 13 processing runs with high and low feed stream Cd concentrations and either RO or city water (CW), are shown in Table 3. It was found that the presence of other cations in the feed stream (use of city water) resulted in a reduction of the removal of the heavy metals by the chelating resin. Use of RO water produced the highest resin capacity with up to 290 times the bed volume being processed before regulatory limits in the outlet stream were reached.
              TABLE 1                                                     
______________________________________                                    
DESIGN PARAMETERS                                                         
Parameter          Quantity                                               
______________________________________                                    
Pilot Plant Operating Schedule                                            
                   24 hrs/day (7 days/week)                               
Wastewater input flow rate                                                
                   150 gpd                                                
Cd.sup.2+  Concentration                                                  
                   23 mg/L                                                
CN- Concentration  23 mg L                                                
Cation Column                                                             
Diameter           3 in                                                   
Length             10 in                                                  
Flow-through Rate  20 BV/hr                                               
Hydraulic Loading  83 L/min-m.sup.2                                       
Resin Capacity     600 meq/L                                              
Bed Volume (BV)    2.2 L/column                                           
Anion Column                                                              
Diameter           4 in                                                   
Length             12 in                                                  
Flow-through Rate  10 BV/hr                                               
Hydraulic Loading  71.3 L/min-m.sup.2                                     
Resin Capacity     400 meq/L                                              
Bed Volume (BV)    2.5 L/column                                           
Electrolytic Recovery Unit                                                
Capacity           20 L                                                   
Cathodes           1 s.f. Stainless Steel                                 
Anodes             1 s.f. Stainless Steel                                 
Rectifier          100 A, 110 V                                           
______________________________________                                    
              TABLE 2                                                     
______________________________________                                    
OPERATING PARAMETERS                                                      
Parameter          Quantity                                               
______________________________________                                    
Cation Columns                                                            
Initial Rinse Flow Rate                                                   
                   0.38 L/min                                             
Initial Rinse Volume                                                      
                   3.5 L                                                  
Regeneration Flow Rate                                                    
                   0.04-0.08 L/min                                        
Acid Requirement   6-12 lbs H.sub.2 SO.sub.4 /ft.sup.3                    
Volume of Regenerant                                                      
                   1.87 L 10% H.sub.2 SO.sub.4 solution                   
Slow Rinse Flow Rate                                                      
                   0.04-0.08 L/min                                        
Slow Rinse Volume  1.2                                                    
Fast Rinse Flow Rate                                                      
                   0.38 L/min                                             
Fast Rinse Volume  10.5 L                                                 
Neutralization Flow Rate                                                  
                   0.04-0.08 L/min                                        
NaOH Requirement   4 lbs NaOH/ft.sup.3                                    
Volume of Neutralization Solution                                         
                   1.32 L 5% NaOH solution                                
Final Rinse Flow Rate                                                     
                   0.38 L/min                                             
Final Rinse Volume 2.5 L                                                  
Anion Columns                                                             
Initial Rinse Flow Rate                                                   
                   0.38 L/min                                             
Initial Rinse Volume                                                      
                   7.4 L                                                  
Regeneration Flow Rate                                                    
                   0.08-0.16 L/min                                        
NaOH Requirement   4 lbs NaOH/ft.sup.3                                    
Volume of Regenerant                                                      
                   3 L                                                    
Slow Rinse Flow Rate                                                      
                   0.08-0.17 L/min                                        
Slow Rinse Volume  2.5 L                                                  
Fast Rinse Flow Rate                                                      
                   0.38 L/min                                             
Fast Rinse Volume  22 L                                                   
______________________________________                                    
Regeneration of the column with H2 SO4 released substantially all of the bound cadmium at a concentration of about 1200 mg/L. Approximately 97% of the cadmium was then recovered as elemental cadmium in an electrolytic recovery unit 30.
Some advantages of the process described above are that, contrary to the referenced literature, metals can be removed from cyanide complexes in water using standard chelating cationic resins in an unconventional manner without resin degeneration or the potential of hydrogen cyanide gas formation and release. At the same time, heavy metals, such as cadmium, are removed in a form suitable for recovery or recycling to the plating baths instead of disposal as toxic sludge.
                                  TABLE 3                                 
__________________________________________________________________________
TEST RESULTS                                                              
            Feed Characterization      Cation Column Results              
                      Cation-  Column Spec.                               
                                       Actual                             
                                            Complete                      
                                                 Regulatory               
                      Cd  Flow Bed                                        
                                  Flow Cd   Break-                        
                                                 Break-                   
Run  Process                                                              
            Cd   Cation                                                   
                      Molar                                               
                          Rate Vol                                        
                                  Rate Capacity                           
                                            through                       
                                                 through                  
Number                                                                    
     Water  (Mg/L)                                                        
                 (meq/L)                                                  
                      Ratio                                               
                          (ml/min)                                        
                               (L)                                        
                                  (BV/hr)                                 
                                       (meq/L)                            
                                            (BV) (BV)                     
__________________________________________________________________________
BC-1 CW low Cd                                                            
            18   14   87  200  1.2                                        
                                  10   --   --   --                       
BC-2 CW low Cd                                                            
            18   14   87  300  1.2                                        
                                  15    75  325  150                      
BC-3 CW low Cd                                                            
            21   14   75  500  1.2                                        
                                  25   --   --   160                      
BC-4 CW low Cd                                                            
            22   12   61  400  2.2                                        
                                  11   --   --   250                      
BC-5 CW low Cd                                                            
            18   12   75  400  2.2                                        
                                  11   --   --   --                       
BC-6 CW low Cd                                                            
            29   16   62  360  2.2                                        
                                  10   140  310  200                      
BC-7 CW low Cd                                                            
            30   15   56  370  2.2                                        
                                  10   230  440  260                      
Average for City                                                          
            22   14   72  361  1.8                                        
                                  13   148  358  204                      
Water Runs with                                                           
Low Cd                                                                    
BC-8 RO Water                                                             
            28   6.1  24  530  2.2                                        
                                  14   340  1140 270                      
BC-9 RO Water                                                             
            28   6.1  24  700  2.2                                        
                                  19   630  1600 290                      
BC-10                                                                     
     RO Water                                                             
            29   6.1  24  700  2.2                                        
                                  19   --   --   290                      
Average for City                                                          
            28   6.1  24  643  2.2                                        
                                  18   485  1370 283                      
Water Runs with                                                           
Low Cd                                                                    
BC-11                                                                     
     RO (D.O.)                                                            
            50   19   43  760  2.2                                        
                                  21   420  750  170                      
BC-12                                                                     
     CW high Cd                                                           
            68   17   28  430  2.2                                        
                                  12   330  380  120                      
BC-13                                                                     
     CW high CD                                                           
            83   19   26  550  2.2                                        
                                  15   520  390  110                      
Average for City                                                          
            76   18   27  490  2.2                                        
                                  13   425  385  115                      
Water Runs with                                                           
Low Cd                                                                    
__________________________________________________________________________
Although the present invention has been described in considerable detail with reference to certain preferred versions and uses thereof, other versions and uses are possible. For example, the process set forth above for recovering cyanide complexed cadmium can be applied to the removal from a solvent system of any ion, such as a metal ion having a positive charge, complexed or chelated with a second ion of an opposite charge, such that the complex or chelate has a neutral charge or a charge opposite to that of the metal ion itself (i.e. a complexed cation has a negative charge), by contacting the complex with a chelating resin with active sites on the resin chelate oppositely charged to the ion if unbound (i.e., the metal ion) and the same charge as the chelated ion. In this manner, negatively or neutrally charged chelates or complexes of various metals including, but not limited to, mercury, copper, gold, silver, lead, nickel, zinc, cobalt, iron, magnesium, cadmium and calcium can be removed from a basic (pH ≧7.0), aqueous feed stream by passing the solution over a cationic chelating resin. While cyanide is a typical complexing agent, one skilled in the art would recognize that the metal may be bound to other complexing or chelating agents. Further, while sulfuric acid is the preferred acid for removing the metal ion from the resin, other acids which form soluble salts with the metal ion may also be used for regeneration of the resin. Further, while sodium hydroxide is the preferred base for converting the chelating resin to the sodium form, other bases which will convert the resin to a usable form may be used. Therefore, the spirit and scope of the appended claims should not be limited to the description of the preferred version contained herein, or the typical operating conditions or design parameters set forth above.

Claims (23)

What is claimed is:
1. A process for removing cations from a negatively charged chelate or complex of the cation with an anion, the complex being dissolved in an aqueous feed stream having a pH greater than 7.0, comprising:
a) passing the aqueous feed stream over a cationic chelating ion exchange resin in the sodium form to release said cation from the complex, binding said cation to the resin and forming an anionic effluent containing the anion as a soluble salt, the effluent being substantially free of said cation, and;
b) regenerating the chelating ion exchange resin by first passing a strong acid solution over the resin to remove substantially all of said cations from the resin, forming an acidic effluent containing a water soluble salt of said cation and then passing a basic solution over said resin to convert the resin to the sodium form.
2. The process of claim 1 wherein said cation is a metal ion.
3. The process of claim 1 wherein said strong acid is sulfuric acid.
4. The process of claim 1 wherein said cation is selected from the group consisting of mercury, copper, lead, nickel, zinc, cobalt, gold, silver, iron, magnesium, cadmium and calcium ions.
5. The process of claim 1 wherein said cation is cadmium and said anion is cyanide.
6. The process of claim 1 wherein the pH of the feed stream is greater than 8.5.
7. A process for removing and recycling cations which are complexed or chelated with an anion, the resultant complex or chelate being dissolved in an aqueous solution having a pH greater than 7.0, comprising:
a) contacting said aqueous solution with a cationic chelating ion exchange resin in the sodium form to release said cation from said complex, binding said cation to the resin and forming an effluent containing said anion, the effluent being substantially free of said cation, and;
b) regenerating said chelating ion exchange resin by first passing a strong acid solution over the resin to remove substantially all of said cations from the resin, forming an acidic effluent containing said cation, and then passing a basic solution over the resin to convert the resin to the sodium form, and;
c) removing said cation from said acidic effluent in an elemental form.
8. The process of claim 7 wherein said cation is a metal ion.
9. The process of claim 7 wherein said strong acid is sulfuric acid.
10. The process of claim 7 wherein said cation is selected from the group consisting of mercury, copper, lead, nickel, zinc, cobalt, gold, silver, iron, magnesium, cadmium and calcium ions.
11. The process of claim 10 wherein said acidic effluent is fed to an electrolytic recovery unit, and said cation is converted to elemental metal.
12. The process of claim 7 wherein the pH of the feed stream is greater than 8.5.
13. A process for removing and recycling cations which are complexed or chelated with an anion, the resultant complex or chelate being dissolved in an aqueous solution having a pH greater than 7.0, comprising:
a) contacting the aqueous solution with a cationic chelating ion exchange resin in the sodium form to release said cation from said complex, binding said cation to the resin and forming an effluent containing said anion, the effluent being substantially free of said cation, and;
b) regenerating the chelating ion exchange resin by first passing a strong acid solution over said resin to remove substantially all of said cations from the resin, forming an acidic effluent containing the cations, and then passing a basic solution over the resin to convert the resin to the sodium form, and;
c) removing said cations from the acidic effluent in an elemental form, and;
d) further processing the effluent to convert the anion to a less toxic form.
14. The process of claim 13 wherein said cation is a metal ion.
15. The process of claim 13 wherein said strong acid is sulfuric acid.
16. The process of claim 13 wherein said cation is selected from the group consisting of mercury, copper, lead, nickel, zinc, cobalt, gold, silver, iron, magnesium, cadmium and calcium ions.
17. The process of claim 13 wherein the pH of the feed stream is greater than 8.5.
18. The process of claim 13 wherein said effluent containing said anion is fed to a processing stage for chlorination and alkali treatment.
19. A process for removing cations from a negatively charged chelate or complex of the cation with an anion, the complex being dissolved in an aqueous feed stream having a pH greater than 7.0, comprising passing the aqueous feed stream over a cationic chelating ion exchange resin in the sodium form to release said cation from the complex, binding said cation to the resin and forming an anionic effluent containing the anion as a soluble salt, the effluent being substantially free of said cation.
20. The process of claim 19 wherein said cation is a metal ion.
21. The process of claim 19 wherein said cation is selected from the group consisting of mercury, copper, lead, nickel, zinc, cobalt, gold, silver, iron, magnesium, cadmium and calcium ions.
22. Process of claim 19 wherein said cation is cadmium and said anion is cyanide.
23. The Process of claim 19 wherein the pH of the feed stream is greater than 8.5.
US08/300,288 1994-08-30 1994-08-30 Ion exchange removal of cations under chelating/complexing conditions Abandoned USH1661H (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
US08/300,288 USH1661H (en) 1994-08-30 1994-08-30 Ion exchange removal of cations under chelating/complexing conditions

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US08/300,288 USH1661H (en) 1994-08-30 1994-08-30 Ion exchange removal of cations under chelating/complexing conditions

Publications (1)

Publication Number Publication Date
USH1661H true USH1661H (en) 1997-07-01

Family

ID=23158481

Family Applications (1)

Application Number Title Priority Date Filing Date
US08/300,288 Abandoned USH1661H (en) 1994-08-30 1994-08-30 Ion exchange removal of cations under chelating/complexing conditions

Country Status (1)

Country Link
US (1) USH1661H (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20060275191A1 (en) * 2005-06-03 2006-12-07 Brookhaven Science Associates, Llc System and method for separating tellurium from cadmium waste
EP1985590A1 (en) 2007-04-27 2008-10-29 Jihoceska Universita V Ceskych Budejovicich The method of treatment of iron-containing waterworks sludge and a mixture prepared by this method

Citations (27)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2980607A (en) * 1957-05-10 1961-04-18 Dow Chemical Co Treatment of aqueous liquid solutions of chelate-forming metal ions with chelate exchange resins
US3148947A (en) * 1956-07-10 1964-09-15 Herbert J Fleischmann Method for the separation of a complexing agent and a metallic ion from their complex
US3969244A (en) * 1970-06-09 1976-07-13 Hokuetsu Carbon Industry Co., Ltd Method of adsorbing heavy metals
US3984314A (en) * 1974-04-22 1976-10-05 Rohm And Haas Company Process for selective removal and recovery of cyanide values by ion exchange
US4123340A (en) * 1976-11-22 1978-10-31 Gotzelmann Kg Industrieabwasser-Anlagen Method and apparatus for treating metal containing waste water
US4159235A (en) * 1976-11-22 1979-06-26 Gotzelmann Kg Method and apparatus for treating metal containing waste water
US4250031A (en) * 1977-03-01 1981-02-10 Unitika Ltd. Phenolic chelate resin and method of adsorption treatment
US4303704A (en) * 1980-05-19 1981-12-01 Courduvelis Constantine I Selective removal of copper or nickel from complexing agents in aqueous solution
US4417987A (en) * 1980-12-12 1983-11-29 Interox Chemicals Limited Process for detoxification
US4448694A (en) * 1981-09-04 1984-05-15 Dow Corning Corporation Metal extraction from solution and immobilized chelating agents used therefor
US4537937A (en) * 1984-02-13 1985-08-27 Olin Corporation Chelating resin and process for making same
US4723998A (en) * 1985-11-29 1988-02-09 Freeport Minerals Co Recovery of gold from carbonaceous ores by simultaneous chlorine leach and ion exchange resin adsorption process
US4863612A (en) * 1987-08-10 1989-09-05 Kinetico, Inc. Apparatus and method for recovering materials from process baths
US4867882A (en) * 1987-11-09 1989-09-19 Aluminum Company Of America Method for reducing the amount of anionic metal ligand complex in a solution
US5055199A (en) * 1987-11-09 1991-10-08 Aluminum Company Of America Method for reducing the amount of anionic metal-ligand complex in a solution
US5073575A (en) * 1988-08-26 1991-12-17 The Regents Of The University Of California Cadmium ion-chelating synthetic polymers and process thereof
US5108615A (en) * 1989-11-28 1992-04-28 Bio-Recovery Systems, Inc. Method for recovery of a metal ion from electroless plating solutions
US5147617A (en) * 1991-05-21 1992-09-15 Freeport-Mcmoran Inc. Process for recovery of gold from gold ores using a complexing pretreatment and sulfurous acid leaching
US5180822A (en) * 1988-09-21 1993-01-19 Reilly Industries, Inc. Highly selective chelating resins and monomers for their preparation
US5187200A (en) * 1991-03-13 1993-02-16 Rainer Norman B Process for the selective absorption of anions
US5198021A (en) * 1992-03-18 1993-03-30 Henkel Corporation Recovery of precious metal
US5200473A (en) * 1988-03-25 1993-04-06 Jeanneret Gris Gilbert Chelating resins and method for their use in the extraction of metal ions
US5215575A (en) * 1989-03-07 1993-06-01 Butler Dean R Recovery of gold, silver and platinum group metals with various leachants at low pulp densities
US5259960A (en) * 1992-06-26 1993-11-09 Man-Gill Chemical Company Regeneration and recycling of contaminated solutions from aluminum and tin washer processes
US5262018A (en) * 1991-08-12 1993-11-16 Fmc Corporation Metals removal from aqueous peroxy acids or peroxy salts
US5269905A (en) * 1990-04-30 1993-12-14 Elf Atochem North America, Inc. Apparatus and process to regenerate a trivalent chromium bath
US5409582A (en) * 1993-01-29 1995-04-25 Monsanto Company Silver bath waste treatment apparatus and method

Patent Citations (28)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3148947A (en) * 1956-07-10 1964-09-15 Herbert J Fleischmann Method for the separation of a complexing agent and a metallic ion from their complex
US2980607A (en) * 1957-05-10 1961-04-18 Dow Chemical Co Treatment of aqueous liquid solutions of chelate-forming metal ions with chelate exchange resins
US3969244A (en) * 1970-06-09 1976-07-13 Hokuetsu Carbon Industry Co., Ltd Method of adsorbing heavy metals
US3984314A (en) * 1974-04-22 1976-10-05 Rohm And Haas Company Process for selective removal and recovery of cyanide values by ion exchange
US4123340A (en) * 1976-11-22 1978-10-31 Gotzelmann Kg Industrieabwasser-Anlagen Method and apparatus for treating metal containing waste water
US4159235A (en) * 1976-11-22 1979-06-26 Gotzelmann Kg Method and apparatus for treating metal containing waste water
US4250031A (en) * 1977-03-01 1981-02-10 Unitika Ltd. Phenolic chelate resin and method of adsorption treatment
US4303704A (en) * 1980-05-19 1981-12-01 Courduvelis Constantine I Selective removal of copper or nickel from complexing agents in aqueous solution
US4417987A (en) * 1980-12-12 1983-11-29 Interox Chemicals Limited Process for detoxification
US4448694A (en) * 1981-09-04 1984-05-15 Dow Corning Corporation Metal extraction from solution and immobilized chelating agents used therefor
US4537937A (en) * 1984-02-13 1985-08-27 Olin Corporation Chelating resin and process for making same
US4723998A (en) * 1985-11-29 1988-02-09 Freeport Minerals Co Recovery of gold from carbonaceous ores by simultaneous chlorine leach and ion exchange resin adsorption process
US4863612A (en) * 1987-08-10 1989-09-05 Kinetico, Inc. Apparatus and method for recovering materials from process baths
US4863612B1 (en) * 1987-08-10 1994-11-01 Kineticon Inc Apparatus and method for recovering materials from process baths
US5055199A (en) * 1987-11-09 1991-10-08 Aluminum Company Of America Method for reducing the amount of anionic metal-ligand complex in a solution
US4867882A (en) * 1987-11-09 1989-09-19 Aluminum Company Of America Method for reducing the amount of anionic metal ligand complex in a solution
US5200473A (en) * 1988-03-25 1993-04-06 Jeanneret Gris Gilbert Chelating resins and method for their use in the extraction of metal ions
US5073575A (en) * 1988-08-26 1991-12-17 The Regents Of The University Of California Cadmium ion-chelating synthetic polymers and process thereof
US5180822A (en) * 1988-09-21 1993-01-19 Reilly Industries, Inc. Highly selective chelating resins and monomers for their preparation
US5215575A (en) * 1989-03-07 1993-06-01 Butler Dean R Recovery of gold, silver and platinum group metals with various leachants at low pulp densities
US5108615A (en) * 1989-11-28 1992-04-28 Bio-Recovery Systems, Inc. Method for recovery of a metal ion from electroless plating solutions
US5269905A (en) * 1990-04-30 1993-12-14 Elf Atochem North America, Inc. Apparatus and process to regenerate a trivalent chromium bath
US5187200A (en) * 1991-03-13 1993-02-16 Rainer Norman B Process for the selective absorption of anions
US5147617A (en) * 1991-05-21 1992-09-15 Freeport-Mcmoran Inc. Process for recovery of gold from gold ores using a complexing pretreatment and sulfurous acid leaching
US5262018A (en) * 1991-08-12 1993-11-16 Fmc Corporation Metals removal from aqueous peroxy acids or peroxy salts
US5198021A (en) * 1992-03-18 1993-03-30 Henkel Corporation Recovery of precious metal
US5259960A (en) * 1992-06-26 1993-11-09 Man-Gill Chemical Company Regeneration and recycling of contaminated solutions from aluminum and tin washer processes
US5409582A (en) * 1993-01-29 1995-04-25 Monsanto Company Silver bath waste treatment apparatus and method

Non-Patent Citations (5)

* Cited by examiner, † Cited by third party
Title
Amber hi lites, No. 162, Ion Exchange in Heavy Metals Removal and Recovery Rohm and Haas; Walter H. Waitz, Jr., pp. 1 8. *
Amber-hi-lites, No. 162, Ion Exchange in Heavy Metals Removal and RecoveryRohm and Haas; Walter H. Waitz, Jr., pp. 1-8.
Amberlite IRC 718 Technical Brochure Rohm and Haas 1993. *
Amberlite IRC-718 Technical Brochure -Rohm and Haas 1993.
Cyanide Removal Technical Brochure Rohm and Haas. *

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20060275191A1 (en) * 2005-06-03 2006-12-07 Brookhaven Science Associates, Llc System and method for separating tellurium from cadmium waste
US7731920B2 (en) * 2005-06-03 2010-06-08 Brookhaven Science Associates System and method for separating tellurium from cadmium waste
US20100189612A1 (en) * 2005-06-03 2010-07-29 Vasilis Fthenakis System and method for separating tellurium from cadmium waste
EP1985590A1 (en) 2007-04-27 2008-10-29 Jihoceska Universita V Ceskych Budejovicich The method of treatment of iron-containing waterworks sludge and a mixture prepared by this method

Similar Documents

Publication Publication Date Title
CA1249885A (en) Membrane processes for metal recovery and pollution control in metal process industries
US4267159A (en) Cyanide recovery
US7488423B2 (en) System and method of slurry treatment
CA2016562C (en) Elution process for gold-iodine complex from ion-exchange resins
US3788983A (en) Selective separation of cyanide from waste streams by adsorption process
US4636288A (en) Electrodialytic conversion of multivalent metal salts
US4009101A (en) Recycle treatment of waste water from nickel plating
US3842000A (en) Process for removal of ammonia from aqueous streams
EP0355418B1 (en) Process for the treatment of effluents containing cyanide and toxid metals, using hydrogen peroxide and trimercaptotriazine
CS245861B1 (en) Method of heavy metals separation from aminocarboxyl complexing substances
US2628165A (en) Process of preventing pollution of streams
US4269716A (en) Ion exchange separation method
USH1661H (en) Ion exchange removal of cations under chelating/complexing conditions
JP3203745B2 (en) Fluorine-containing water treatment method
CA2016561C (en) Purification process for gold-bearing iodine lixiviant
Germain et al. Plating and cyanide wastes
JPH11235595A (en) Treatment of boron-containing waste water
RU2097438C1 (en) Method of recovering metals from scrap
JP3981318B2 (en) Treatment method of electroless nickel plating aging solution
Chang et al. Alternative waste minimization analyses for the printed circuit board industry: Examples for small and large manufacturers
JPH11207365A (en) Treatment of selenium-containing waste water
JP2535937B2 (en) Cyan-containing wastewater treatment method
GB2406565A (en) A method for refining an aqueous nickel chloride solution
Jeon Review for physical and chemical process for heavy metal treatment
JPH10314797A (en) Method for treating water containing fluoride ion and cod component

Legal Events

Date Code Title Description
AS Assignment

Owner name: UNITED STATES OF AMERICA, THE, AS REPRESENTED BY T

Free format text: ASSIGNMENT OF ASSIGNORS INTEREST;ASSIGNORS:KOFF, JENNIE L.;ZARATE, DANIEL A.;REEL/FRAME:007138/0888

Effective date: 19940829

STCF Information on status: patent grant

Free format text: PATENTED CASE