U.S. patents available from 1976 to present.
U.S. patent applications available from 2005 to present.

Process for insolubilizing potentially water pollutable wastes from sodium or ammonium type sulfur dioxide air pollution control systems

Patent 3984312 Issued on October 5, 1976. Estimated Expiration Date: Icon_subject October 5, 1993. Estimated Expiration Date is calculated based on simple USPTO term provisions. It does not account for terminal disclaimers, term adjustments, failure to pay maintenance fees, or other factors which might affect the term of a patent.

Patent References

2296423

3468797

3505008

3617559

3720609

3763038

3785840

3859799

Inventors

Assignee

Application

No. 411367 filed on 10/31/1973

US Classes:

210/620, Aerobic treatment210/717, In situ210/737, Including temperature change423/140, Forming insoluble substance in liquid423/143, Utilizing or forming nitrogenous compound423/144, Carbonating, hydroxylating, or hydrating423/145, Sulfating423/146, Sulfating423/202, Treating with acid or acid salt423/548, Using metal sulfate as reactant423/556, Aluminum containing423/558, Iron containing588/252, Solidification, vitrification, or cementation588/318, Detoxification by using acid or alkaline reagents (EPO/JPO)588/320, By oxidation; by combustion (EPO/JPO)588/404, Toxic combustion residues, e.g., toxic substances contained in fly ash from waste incineration (EPO/JPO)588/407, Containing heavy metals (EPO/JPO)588/412Containing heavy metals, in the bonded or free state (EPO/JPO)

Examiners

Primary: Hart, Charles N.
Assistant: Hruskoci, Peter A.

Attorney, Agent or Firm

Abstract

Process for insolubilizing water soluble wastes from alkaline sodium or ammonium type sulfur dioxide control systems used in conjunction with industrial or power plants. The sodium or ammonium sulfite or sulfate wastes are reacted in solution with ferric ions and sulfuric acid to produce an insoluble basic, hydrous or anhydrous, sodium and/or ammonium hydroxy ferric sulfate or sulfite compounds of the generic type Mv (Na, NH4)w Fex (SOu)y (OHz)nH2 O, wherein M is selected from an alkali metal other than sodium, or an authigenic metal or other cation present in industrial or power plant wastes, v is selected from zero to six, w is selected from zero to five, x is selected from zero to six, y is selected from one to five, u is 3 and/or 4, z is selected from zero to 12, and n is selected from zero to 20. Principal end product compounds include Natrojarosite, Ammoniojarosite, Metasideronatrite, Sideronatrite, Depegite, Rosarite, Iriite, and mixtures thereof. The reaction takes place at an acid pH in a temperature ranging from about 50°-300° F. and may occur in single or multi-stage reactors. Air and/or bacterial activation at a pH of less than about 5.5 may be employed. The end product basic, sodium and/or ammonium hydroxy ferric sulfate and sulfite compounds are water insoluble as compared to the standard in the industry, CaSO4, and may be disposed of by simple landfill without the water pollution hazards inherent with landfilling of wet or dry sodium or ammonium sulfite and/or sulfate baghouse or wet scrubber wastes. The process also uses, and conversely can dispose of, other pollutants as reactants, such as hot waste water from power plant ash tanks, waste sulfuric acid, pickle liquior, acid mine water (blackwater), iron slag or scrap, or gob or pyrite leachate as part of an integrated, multiple-pollutant disposal process.

Other References

  • Mellor, "A Comprehensive Treatise on Inorganic & Theoretical Chemistry," vol. 14 p. 345
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