Method for ammonia recovery from contaminated water including solvay effluent and aqueous solutions

Patent metadata

Field	Value
Publication number	US-11453951-B1
Application number	US-202117340694-A
Country	US
Kind code	B1
Filing date	Jun 7, 2021
Priority date	Jun 7, 2021
Publication date	Sep 27, 2022
Grant date	Sep 27, 2022

Abstract

This invention describes a novel recovery method of ammonia through the electrocoagulation process, which may be applied in the industrial as well as the environmental sectors. The present invention has a significant impact not only on recovering the ammonia content from the Solvay effluent, but also for recovering the ammonia from landfill leachate and different sources of wastewater where high concentrations of ammonia can be found. This invention has economic benefits in recovering ammonia and reducing the required energy in such processes. Another impact is the environmental one, where ammonia can cause problems such as toxicity to the organisms living in the soil or water bodies, and could also decrease the concentration of the dissolved oxygen.

First claim

What is claimed is:

1. A method for ammonia recovery from contaminated water including an effluent solution comprising ammonia (NH 4 OH), magnesium carbonate, and high salinity brine, and aqueous solutions, wherein the method comprises a first process comprising the steps of:
adding calcium oxide to the effluent solution at a concentration from about 0.5% to about 10%;
applying an electrocoagulation process to the solution with aluminum electrodes and a current density of about −5 to about 15 mA/cm 2 -over 4-9 hours; and
applying air bubbling through the solution at gas flow rate of 100 to 300 ml/min in a treating cell with one air inlet and one ammonia gas exit outlet for stripping ammonia from the solution, wherein ammonia is recovered from ammonium chloride or ammonium hydroxide in a brine mixture using calcium oxide and electrocoagulation process, wherein the recovery efficiency is between about 90 to about 99%.

2. The method of claim 1 , wherein the method further comprises a second process comprising the steps of:
reacting the solution form the first process with carbon dioxide;
filtrating the solution to recover solids precipitates;
adding calcium hydroxide to the filtrate solution to obtain a pH higher than 11; and
introducing the solution inside the electrocoagulation cell.

3. The method of claim 1 , further comprising mixing calcium oxide to ammonium chloride and brine mixture to enhance ammonia recovery in the electrocoagulation step with an NH 3 :Ca(OH) 2 molar ratio of about 2 to about 1.

4. The method of claim 2 , wherein the molar ratio is about 2:1.

5. The method of claim 1 , wherein the solution comprises brine and ammonia and further Ca(OH) 2 is added to the electrocoagulation cell and the electrocoagulation cell has an inlet for air and one outlet for ammonia gas.

6. The method of any of the preceding claims, wherein the concentration of ammonium chloride in the effluent solution is in the range of about 12,000 to about 20,000 mg N/L.

7. The method of any of the preceding claims, wherein the concentration of ammonium chloride in the effluent is decreased to less than 10% by weight.

8. The method of any of the preceding claims, wherein ammonia can be recovered from water solution containing ammonium hydroxide with recovery efficiency of more than 77%.

9. The method of claim 1 , where an electrocoagulation cell is used in the presence of calcium hydroxide without any additional heating to enhance the ammonia dissociation and stripping.

10. The method of claim 5 , wherein the brine is real reject brine with a total salinity of about 70,000 to about 75,000 ppm and a pH value of about 8.6 to about 8.8.

11. The method of claim 10 , comprising mixing 25 wt % ammonium hydroxide solution to the brine to recover solid magnesium hydroxide with a NH 3 :Mg molar ratio of about 3 to about 4.

12. The method of claim 10 , further comprising mixing calcium oxide to ammonium chloride and brine mixture to enhance ammonia recovery in the electrocoagulation step with a NH 3 to Ca(OH) 2 molar ratio of about 2:1.

13. The method of claim 1 , wherein the gas flow of air to enhance the stripping of ammonia gas through the electrocoagulation process comprises an inert or reactive gas such as effluent gas or flare gas.

14. The method of claim 1 , wherein the air inlet is immersed in the solution comprising brine near the bottom of the electrocoagulation cell and the ammonia gas exit outlet is a tube which is extended from the top of the cell and the process of ammonium removal includes oxygen generation at the anode at a high pH level and enough anodic potential, to generate ammonia and hydrogen gases at the cathode.

15. The method of claim 2 , wherein ammonium removal includes oxygen generation at the anode at a pH of about 10.5 to 11.5.

16. The method of claim 1 , wherein the process temperature range is 35 to 40° C. at the current density of about 5 to about 15 mA/cm 2 .

17. The method of claim 1 , wherein an energy demand is about 1.5 to 2.5 KW h/Kg NH 3 .

18. The method of claim 1 , wherein the ammonia gas leaves the electrocoagulation cell, through a gas exit outlet-, and dissolves in a closed-cell containing deionized water at room temperature.

Assignees

• Univ United Arab Emirates

Inventors

• Mohammad Ameera
• Al Marzouqi Ali
• El Naas Muftah

Classifications

• C02F2001/46133

  characterised by the material · CPC title

• C02F1/66

  by neutralisation; pH adjustment (for degassing C02F1/20; using ion-exchange C02F1/42; for flocculation or precipitation of suspended impurities C02F1/52; for removing dissolved compounds C02F1/58) · CPC title

• C02F1/463

  by electrocoagulation · CPC title

• C02F1/20

  by degassing, i.e. liberation of dissolved gases (degasification of liquids in general B01D19/00; arrangement of degassing apparatus in boiler feed supply F22D) · CPC title

• C02F1/001

  Processes for the treatment of water whereby the filtration technique is of importance (C02F1/44 takes precedence; construction of filters in general B01D24/00 - B01D41/00) · CPC title