Methods and systems for treating produced water
US-2015376033-A1 · Dec 31, 2015 · US
US2019270656A1 · US · A1
| Field | Value |
|---|---|
| Publication number | US-2019270656-A1 |
| Application number | US-201716348242-A |
| Country | US |
| Kind code | A1 |
| Filing date | Nov 9, 2017 |
| Priority date | Nov 10, 2016 |
| Publication date | Sep 5, 2019 |
| Grant date | — |
A practical reading order for non-experts. Skip the full description unless you need deep technical detail.
What the patent document calls the invention.
A short plain-language summary of the technical disclosure.
Who owns or filed the patent and who is credited as inventor.
Filing, priority, publication, and grant dates set the timeline.
The legal scope of protection — read this for what is actually claimed.
Technology tags used to group this patent with similar filings.
Prior art links and similar publications in this corpus.
Official abstract text for this publication.
A process for reducing the concentration of one or more arsenic-containing compounds in an aqueous solution comprising at least one fluoroacid, which process comprises: (i) contacting the aqueous solution with an oxidising agent to produce one or more Asv-containing compounds; and (ii) removal of precipitated arsenic-containing compounds; wherein the process comprises a step (iii) the addition of an aqueous alkali solution or slurry, which may take place after step (i) and before step (ii) or after step (ii).
Opening claim text (preview).
1 . A process for reducing the concentration of one or more arsenic-containing compounds in an aqueous solution comprising at least one fluoroacid, which process comprises: (i) contacting the aqueous solution with an oxidising agent to produce one or more As V -containing compounds; and (ii) removal of precipitated arsenic-containing compounds; wherein the process comprises a step (iii) the addition of an aqueous alkali solution or slurry, which may take place after step (i) and before step (ii) or after step (ii). 2 . A process according to claim 1 , wherein the aqueous solution comprises fluorosilicic acid. 3 . A process according to claim 1 or 2 , wherein the fluoroacid is present in an amount of from about 1 to about 50% by weight based on the total weight of the aqueous solution. 4 . A process according to any of the preceding claims, wherein the one or more arsenic-containing compounds comprise AsF 3 or a hydrolysed form of AsF 3 . 5 . A process according to any of the preceding claims, wherein the oxidising agent is selected from chlorine (Cl 2 ), hypochlorite salts (M + ClO − ), hypochlorous acid (HClO), hydrogen peroxide (H 2 O 2 ) and permanganate salts (M + MnO 4 − ) and mixtures thereof. 6 . A process according to any of the preceding claims, wherein the removal of the precipitated arsenic-containing compounds comprises gravity-settling, filtration, anion-exchange resin or a combination thereof. 7 . A process according to any of claims 1 to 6 , wherein step (ii) is preceded by the addition of an aqueous alkali solution or slurry. 8 . A process according to any of claims 1 to 6 , wherein step (ii) is followed by the addition of an aqueous alkali solution or slurry. 9 . A process according to any of the preceding claims, wherein the alkali is calcium hydroxide (Ca(OH) 2 ) or calcium oxide (CaO). 10 . A process according to claim 9 , wherein the calcium hydroxide or calcium oxide is present in an amount of from about 15 to about 20% by weight of the solution or slurry. 11 . A process according to any of the preceding claims, further comprising dilution of the solution prior to the addition of the alkali solution or slurry. 12 . A process according to claims 8 to 11 comprising a subsequent step (iv) of removal of the resulting precipitate. 13 . A process according to any of the preceding claims, wherein the addition of the oxidising agent is carried out at a temperature of from about 0 to about 35° C. 14 . A process according to any of the preceding claims, wherein step (i) is carried out in a time period of from about 1 to about 30 minutes. 15 . A process according to claim 14 , wherein step (i) is carried out in a time period of from 2 to 5 minutes. 16 . A process according to any preceding claim, wherein in step (i) the oxidising agent is used in a stoichiometric excess relative to the quantity of oxidisable arsenic-containing compounds. 17 . A process according to claim 16 , wherein the stoichiometric excess is 4 to 60 times the quantity of oxidisable arsenic-containing compounds. 18 . A process according to claim 17 , wherein the stoichiometric excess is 20 to 40 times the quantity of oxidisable arsenic-containing compounds. 19 . A process according to any of the preceding claims, wherein step (iii) is carried out at a temperature of from about 0 to about 35° C. 20 . A process according to claim 18 or 19 , wherein step (iii) is carried out at a temperature of from about 15 to about 30° C. 21 . A process according to any of the preceding claims comprising subsequently recycling all or part of the treated aqueous solution and repeating a process as defined in any one of claims 1 to 20 . 22 . A process according to any of the preceding claims, wherein from about 50 to about 100% by weight of the arsenic-containing compounds is removed from the solution. 23 . A process according to any of the preceding claims, wherein the treated solution contains about 5 ppm or less of arsenic-containing compounds. 24 . A process according to any of the preceding claims, wherein the treated solution contains about 1 ppm or less of arsenic-containing compounds. 25 . A process for the production of fluorosilicic acid comprising a process as defined in any of the preceding claims. 26 . A process for the purification of fluorosilicic acid comprising a process as defined in any of the preceding claims. 27 . A process for the production of HF comprising a process as defined in any of the preceding claims. 28 . A process for the production of aluminium trifluoride (AlF 3 ) comprising a process as defined in any of the preceding claims.
using basic salts, e.g. of aluminium and iron · CPC title
from industrial activities not provided for in groups C02F2103/12 - C02F2103/32 · CPC title
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
Arsenic compounds · CPC title
with halogens or compounds of halogens {(C02F1/4674 takes precedence)} · CPC title
Related publications grouped by family.
Answers are generated from the same data shown on this page.