Device and method for preparing sulfite
US-2022259059-A1 · Aug 18, 2022 · US
US12398045B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-12398045-B2 |
| Application number | US-202017626109-A |
| Country | US |
| Kind code | B2 |
| Filing date | Apr 22, 2020 |
| Priority date | Jul 10, 2019 |
| Publication date | Aug 26, 2025 |
| Grant date | Aug 26, 2025 |
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 device for preparing a sulfite includes: a mother liquid tank and alkaline bin connected to a concentrated alkaline tank, connected to a tower reactor first reactor, one first reactor bottom output end is connected to a first gas-and-liquid mixer and another to a bubbling reaction kettle upper end, a bubbling reaction kettle gas output end is connected to the first mixer being connected to a first reactor upper portion; first reactor upper portion gas and second reactor bottom output ends are connected to a second mixer being connected to the second reactor top; and the bubbling reaction kettle is connected to a centrifugal machine or the alkaline tank, the machine being connected to a wet material bin and the liquid tank. A method includes preparing main and auxiliary absorption liquids, generating a middle slurry, reabsorbing residual gas SO 2 , generating a target product, separating the target product, drying and packaging.
Opening claim text (preview).
What is claimed is: 1. A method for preparing sodium sulfite by using a device, comprising the following steps wherein the device comprises: output ends of a mother liquor tank and an alkali storage A connected to a concentrated alkali tank, a liquid-phase output end of the concentrated alkali tank is connected to a first-stage reactor of a column reactor, one output end at the bottom of the first-stage reactor is connected to a first-stage gas-liquid mixer, the other output end is connected to an upper end of a bubbling reactor, a gas output end at the top of the bubbling reactor is connected to the first-stage gas-liquid mixer, the first-stage gas-liquid mixer is also connected to the top of the first-stage reactor, a gas output end at the top of the first-stage reactor and an output end at the bottom of a second-stage reactor are connected to a second-stage gas-liquid mixer, and the second-stage gas-liquid mixer is connected to the top of the second-stage reactor; a liquid-phase output end of the bubbling reactor is connected to a centrifuge or the concentrated alkali tank, a solid output end of the centrifuge is connected to a wet silo, and a liquid output end of the centrifuge is connected to the mother liquor tank; an output end of the wet silo is connected to a dryer, a gas-phase output end of the dryer is connected to a baghouse dust collector, and an output end at the bottom of the baghouse dust collector outputs a target product; and the bubbling reactor is configured with all or any one or more of a stirring paddle, a water cooling system, a heating system, and a vacuumizing system 1) preparation of main absorption liquid: preparing a thick slurry with a temperature of 45-57° C. and a relative density of 1.28-1.35 in the concentrated alkali tank from desalted water and sodium carbonate when the device runs for the first time or after a major repair; and preparing a thick slurry with a temperature of 42-57° C. and a relative density of 1.45-1.55 in the concentrated alkali tank by using a mother liquor of saturated sodium sulfite as a solvent and sodium carbonate as a solute in the normal production process; 2) preparation of auxiliary absorption liquid: dissolving sodium carbonate with desalted water and condensed water from a drying system to prepare a dilute lye with a temperature of 42-57° C. and a relative density of 1.25-1.33 in a dilute alkali tank; 3) production of intermediate slurry: transferring the prepared slurry in step 1) into the first-stage reactor of the column reactor by using a concentrated alkali pump to undergo counter-current contact reaction with SO 2 raw material gas to produce an intermediate slurry of sodium sulfite and sodium bisulfite; 4) re-absorption of residual SO 2 gas: transferring the dilute lye prepared in step 2) into the second-stage reactor of the column reactor by using a dilute alkali pump to react with residual gas from the first-stage reactor, reducing the volume concentration of SO 2 in the residual gas from the first-stage reactor to 0.3% or less, transferring the absorption liquid in the second-stage reactor into the mother liquor tank by using a second-stage circulating pump when the pH value thereof is reduced to 6.8-7.8, and then turning on a dilute alkali pump and adding the same amount of absorption liquid into the second-stage reactor; 5) preparation of target product slurry: transferring the intermediate slurry obtained in step 3) into the mother liquor tank, preparing a sodium sulfite solution with a relative density of 1.32-1.62 and a pH value of 8-12 in the concentrated alkali tank from the slurry in the mother liquor tank, a lye in the alkali storage A, and fresh desalted water; and for the adjustment of pH, adjusting the pH value of the slurry to 6-8 with solid sodium carbonate or adjusting the pH value of the slurry to 6-8 with a concentrated sodium carbonate slurry with a mass concentration of 15-35%, and then adjusting the pH value to 8-12 with a sodium hydroxide solution with a mass concentration of 20-30%; 6) concentration and crystallization of target product: transferring the suspension obtained in step 5) into the bubbling reactor by using the concentrated alkali pump for cooking with a cooking temperature controlled to 50-75° C. or 98-105° C. and a gas-phase space pressure in the bubbling reactor controlled to an absolute pressure of 15-40 kPa or 100-120 kPa, until the relative density of the slurry in the bubbling reactor reaches 1.48-1.96 and the volume content of crystal particles larger than 150 mesh in the slurry reaches 20-50%; 7) separation of target product: transferring the suspension obtained in step 6) into the centrifuge to undergo separation by the centrifuge to obtain a wet product and a mother liquor of saturated sodium sulfite; and 8) drying and packaging: drying and packaging the wet product obtained in step 7) to obtain a sodium sulfite product. 2. The method according to claim 1 , wherein mass transfer and heat transfer of gas and liquid phases in the first-stage reactor and the second-stage reactor are achieved through pump circulation. 3. The method according to claim 1 , wherein gas-phase substances and liquid-phase substances are in counter-current contact in the method.
Related publications grouped by family.
Answers are generated from the same data shown on this page.