US2020131037A1PendingUtilityA1
Technology of iodine extracting from formation and associated water of oil and gas fields
Est. expiryOct 24, 2039(~13.2 yrs left)· nominal 20-yr term from priority
C01B 7/14C02F 2103/10C02F 2001/5218C02F 1/02C02F 9/00C02F 2209/06C02F 2209/02C02F 1/40C02F 1/76C02F 2101/12C02F 1/66C02F 1/20B01D 2251/304B01D 53/1418C02F 1/281B01D 2251/604
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Claims
Abstract
The present invention relates to a method for extracting iodine from an aqueous brine, the method comprising the steps: Providing an aqueous brine containing iodide ions; Heating the aqueous brine containing iodide ions; Adding an acid to the aqueous brine to arrive at a pH value from 2 to 4; Adding an oxidizing agent to the aqueous brine; Desorbing iodine by means of an airflow; Adding a sorbent for chemisorbing the iodine; Crystallizing the iodine; Purifying the iodine under a layer of sulfuric acid; Sublimation of the iodine.
Claims
exact text as granted — not AI-modified1 . Method for extracting iodine from an aqueous brine, the method comprising the steps:
Providing an aqueous brine; Heating the aqueous brine; Adding an acid to the aqueous brine to arrive at a pH value from 2 to 4; Adding an oxidizing agent to the aqueous brine to form iodine from iodide contained in the brine; Desorbing the iodine by means of an airflow; Adding a sorbent for chemisorbing the iodine; Crystallizing the iodine; Purifying the iodine under a layer of sulfuric acid; Sublimation of the iodine.
2 . Method according to claim 1 , wherein the aqueous brine is formation and associated waters from oil and gas fields.
3 . Method according to claim 1 , wherein the aqueous brine comprises the iodide ions in an amount of at least 20 mg/l, with respect to the total volume of the aqueous brine.
4 . Method according to claim 1 , wherein heating the aqueous brine comprises heating to a temperature from 45 to 50° C.
5 . Method according to claim 1 , wherein the pH of the aqueous brine after adding the acid is from 2.5 to 3.5.
6 . Method according to claim 1 , wherein the acid is sulfuric acid and/or hydrochloric acid.
7 . Method according to claim 1 , wherein the oxidizing agent is chlorine or chlorine water.
8 . Method according to claim 1 , wherein the desorbing is carried out in a vertical column apparatus filled with a desorber packing.
9 . Method according to claim 1 , wherein the desorbing is carried out with an airflow rate in the range from 105 to 150 m 3 /m 3 , with respect to the volume of the aqueous brine.
10 . Method according to claim 8 , wherein a water density of the desorber packing is 60 m 2 /m 3 , with respect to the vertical column apparatus cross-section square.
11 . Method according to claim 1 , wherein the sorbent is sodium hydroxide and or iodine-hydrogen and sulfuric acids.
12 . Method according to claim 1 , wherein the purifying of the iodine under a layer of sulfuric acid is carried out at a the temperature of 100 to 160° C.
13 . Reactor system for carrying out the method according to claim 1 , comprising:
a water heater ( 2 ); a tank for storing an oxidizing agent ( 6 ); means for carrying out iodine oxidation ( 8 ); a desorber ( 5 ); an absorption column ( 15 ); a crystallizer ( 19 ); an iodine melting node ( 21 ); and a sublimator ( 22 ).
14 . Method according to claim 9 , wherein a water density of the desorber packing is 60 m 2 /m 3 , with respect to the vertical column apparatus cross-section square.Join the waitlist — get patent alerts
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