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US4602994A Expired / Lapsed US ⏱️ 0.0 years remaining

Removal of PCBs and other halogenated organic compounds from organic fluids

Assignee: Calspan Corp
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Filing: 1983-10-24
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Granted: 1986-07-29
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Expires: 2003-10-24
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Abstract

Abstract Organic functional fluids containing halogenated organic compounds present as contaminants therein are treated in an inert atmosphere with a NaPEG decomposition reagent which is prepared in an inert atmosphere, thereby to produce a functional fluid phase substantially free of the halogenated organic compound and a reagent residue phase containing a derivative of the contaminant having a reduced halogen content. The latter may be further dehalogenated by reacting the reagent residue with a NaPEG reagent in the presence of oxygen.

Inventors

  • 👤 Louis L. Pytlewski
  • 👤 Frank J. Iaconianni
  • 👤 Kenneth Krevitz
  • 👤 Arthur B. Smith

Bibliographic Details

Application Number —
Jurisdiction US
Data Source google_patents
Last Synchronized 2026-11-02 18:43
CPC Classifications
C; C08; C08G; C08G65/00; C08G65/02; C08G65/32; C08G65/321; A; A62; A62D; A62D3/00; A62D3/30; A62D3/34; A62D3/38; A62D2101/00; A62D2101/20; A62D2101/22; A62D2101/28; A62D2203/00; A62D2203/02; A62D2203/04; Y; Y10; Y10S; Y10S210/00; Y10S210/902; Y10S210/908; Y10S210/909

Claims Analysis

Total Claims: 18
Claim 1
Independent Claim 241 words
A method for the removal of a halogenated organic compound from an organic fluid containing said compound, comprising the steps of: (a) providing a decomposition reagent comprising the product of the reaction of a first reactant selected from the group consisting of an alkali metal, or alloys of said metals, or an alkali metal hydroxide or mixtures of said hydroxides, a second reactant having the general formula ##STR2## wherein R is hydrogen or lower alkyl, R 1 and R 2 are the same or different and are selected from the group consisting of hydrogen, unsubstituted or substituted lower alkyl, unsubstituted or substituted cycloalkyl having from 5 to 8 carbon atoms, and unsubstituted or substituted aryl, n has a value from about 2 to about 400 and x has a value of at least 2, said reaction being carried out in an inert atmosphere; (b) mixing said reagent with said fluid containing said halogenated compound in an inert atmosphere under reactive conditions to form a derivative of said halogenated organic compound, having a reduced halogen content, and a reagent residue, the reagent residue being substantially immiscible with said fluid, and said derivative being more soluble in said reagent residue than in said fluid; (c) allowing said mixture to separate into a two-phase system comprising a reagent residue phase containing said derivative and a fluid phase substantially free of said halogenated compound; and (d) separating said reagent residue phase from said fluid phase.
Claim 2
Independent Claim 241 words
A method for the removal of a halogenated organic compound from an organic fluid containing said compound, comprising the steps of: (a) providing a decomposition reagent comprising the product of the reaction of a first reactant selected from the group consisting of an alkali metal, or alloys of said metals, or an alkali metal hydroxide or mixtures of said hydroxides, a second reactant having the general formula ##STR2## wherein R is hydrogen or lower alkyl, R 1 and R 2 are the same or different and are selected from the group consisting of hydrogen, unsubstituted or substituted lower alkyl, unsubstituted or substituted cycloalkyl having from 5 to 8 carbon atoms, and unsubstituted or substituted aryl, n has a value from about 2 to about 400 and x has a value of at least 2, said reaction being carried out in an inert atmosphere; (b) mixing said reagent with said fluid containing said halogenated compound in an inert atmosphere under reactive conditions to form a derivative of said halogenated organic compound, having a reduced halogen content, and a reagent residue, the reagent residue being substantially immiscible with said fluid, and said derivative being more soluble in said reagent residue than in said fluid; (c) allowing said mixture to separate into a two-phase system comprising a reagent residue phase containing said derivative and a fluid phase substantially free of said halogenated compound; and (d) separating said reagent residue phase from said fluid phase.
Claim 3
Dependent Claim 35 words
The method of claim 1, wherein the decomposition reagent is produced and the derivative of the organic halogenated compound is formed in an inert atmosphere selected from the group consisting of nitrogen, helium or argon.
Claim 4
Dependent Claim 89 words
The method of claim 2, wherein (i) said decomposition reagent is formed from a first reactant selected from the group consisting of lithium, sodium, potassium, or the hydroxides of said metals, or alloys of said metals, or mixtures of said hydroxides, and a second reactant having the formula set forth in claim 1 wherein R 1 and R 2 are hydrogen and x is 2, and (ii) said halogenated organic compound is selected from the group consisting of hexachlorocyclohexane, hexachlorobenzene, trichlorobenzene, tetrachlorobenzene, dichlorophenol, pentachlorophenol, dichlorodiphenyltrichloroethane, decachlorooctahydro-1,3,4-metheno-2H-cyclobuta-[c,d]-pentalen-2-one and polychlorinated biphenyl.
Claim 5
Dependent Claim 18 words
The method of claim 3, wherein said first reactant is sodium and said second reactant is polyethylene glycol.
Claim 6
Dependent Claim 13 words
The method of claim 4, wherein the halogenated organic compound is polychlorinated biphenyl.
Claim 7
Dependent Claim 18 words
The method of claim 3, wherein said first reactant is potassium and said second reactant is polyethylene glycol.
Claim 8
Dependent Claim 13 words
The method of claim 6, wherein the halogenated organic compound is polychlorinated biphenyls.
Claim 9
Dependent Claim 20 words
The method of claim 3, wherein said first reactant is a sodium-potassium alloy and said second reactant is polyethylene glycol.
Claim 10
Dependent Claim 13 words
The method of claim 8, wherein the halogenated organic compound is polychlorinated biphenyl.
Claim 11
Dependent Claim 25 words
The method of claim 1, wherein the fluid containing said halogenated organic compound comprises a non-polar fluid in which said halogenated organic compound is miscible.
Claim 12
Dependent Claim 13 words
The method of claim 10, wherein said non-polar fluid comprises a hydrocarbon-based oil.
Claim 13
Dependent Claim 25 words
The method of claim 1, wherein said fluid containing said halogenated organic compound comprises an aprotic polar fluid in which said halogenated compound is miscible.
Claim 14
Dependent Claim 34 words
The method of claim 1, including the step of further treating said derivative of reduced halogen content in said reagent residue phase with a detoxification agent to effect substantially complete dehalogenation of said derivative.
Claim 15
Dependent Claim 84 words
The method of claim 13, wherein said further treatment comprises reacting said derivative of reduced halogen content in the presence of oxygen with a detoxification agent formed from a first reactant selected from the group consisting of lithium, sodium, potassium, or the hydroxides of said metals, or alloys of said metals, or mixture said hydroxides, a second reactant having the formula set forth in claim 1 wherein R 1 and R 2 are hydrogen and x is 2, and oxygen as a third reactant.
Claim 16
Dependent Claim 18 words
The method of claim 14, wherein said first reactant is sodium and said second reactant is polyethylene glycol.
Claim 17
Dependent Claim 18 words
The method of claim 14, wherein said first reactant is potassium and said second reactant is polyethylene glycol.
Claim 18
Dependent Claim 23 words
The method of claim 14, wherein said first reactant is an alloy of sodium and potassium and said second reactant is polyethylene glycol.

USPTO Annuity & Maintenance Windows

Annuity Stage Window Opens Payment Deadline Surcharge Period Until Estimated Fee Status
3.5 Years (Year 4) 1989-07-28 1990-01-27 1990-07-29 $2000.00 Window Closed / Lapsed
7.5 Years (Year 8) 1993-07-28 1994-01-27 1994-07-29 $3760.00 Window Closed / Lapsed
11.5 Years (Year 12) 1997-07-28 1998-01-27 1998-07-29 $7700.00 Window Closed / Lapsed

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