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Process control of continuous sodium-limestone flue gas desulfurization system

  • US 4,431,618 A
  • Filed: 10/12/1982
  • Issued: 02/14/1984
  • Est. Priority Date: 10/12/1982
  • Status: Expired due to Term
First Claim
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1. In a sodium-limestone double alkali process for the continuous desulfurization of flue gas, having the steps of absorbing sulfur dioxide from a SO2 -containing gas stream in an absorber with an aqueous solution of sodium sulfite and sodium bisulfite, diverting at least a portion of the absorber effluent solution for regeneration with limestone, introducing limestone into the diverted absorber effluent solution to convert bisulfite to sulfite, separating byproduct solids from the limestone-treated solution, and returning regenerated solution to the absorber, the improvement for controlling the continuous, integrated operation of the absorption and regeneration which comprises(a) diverting absorber effluent solution for limestone regeneration, such absorber effluent solution having a pH in the range of from 5.5-6.7;

  • (b) introducing into the diverted absorber effluent solution less than a stoichiometric amount of ground limestone, based on the theoretical calcium carbonate required to completely neutralize the bisulfite content of such absorber solution to sulfite, to maintain the pH of the regenerated solution at a higher pH value within the range of 6.2-7.0 and to convert from 20-70% of the solution bisulfite content to sulfite;

    (c) controlling the limestone addition primarily via either(i) feed forward pH measurements of the diverted absorber effluent solution, the flow of diverted absorber solution being maintained at a relatively constant rate, or(ii) feed forward flow measurements of the diverted absorber effluent solution, the flow of diverted absorber effluent solution being adjusted automatically to provide a relatively constant absorber effluent solution, pH, with feedback pH measurements of the limestone-treated solution being used to provide trimming control of the limestone addition; and

    (d) compensating for process losses of sodium values by adding soda ash or sodium hydroxide at a rate sufficient to maintain the system solution active sodium content at a value within the range of 0.2-2 M, measured as the sum of the bisulfite molar concentration plus twice the sulfite molar concentration of the absorber effluent solution.

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