Claims
- 1. A bleaching composition comprising:
- (a) an oxidatively stable activator having the structure ##STR8## wherein Y.sub.1, Y.sub.3 and Y.sub.4 each represents a bridging group having zero, one, two or three carbon containing nodes for substitution, and Y.sub.2 is a bridging group having at least one carbon containing node for substitution, each said node containing a C(R), [C(R.sub.1)(R.sub.2),] or a C(R).sub.2 unit and each R substituent is the same or different from the remaining R substituents and (i) is selected from the group consisting of methyl, cycloalkyl, cycloalkenyl, alkenyl, aryl, alkynyl, alkylaryl, halogen, alkoxy, phenoxy, CH.sub.2 CF.sub.3, CF.sub.3 and combinations thereof, or (ii) form a substituted or unsubstituted benzene ring of which two carbon atoms in the ring form nodes in the Y unit, or (iii) together with a paired R substituent bound to the same carbon atom form a cycloalkyl or cycloalkenyl ring, which may include an atom other than carbon; M is a transition metal with oxidation states of I, II, III, IV, V, VI, VII or VIII or selected from Groups 3, 4, 5, 6, 7, 8, 9, 10, 11 and 12 of the Periodic Table ofthe Elements; and Q is any counterion which would balance the charge of the compound on a stoichiometric basis; and
- (b) an amount of a source of an oxidant effective for oxidizing byproducts of the pulp and paper making process.
- 2. The composition of claim 1 further comprising a further adjunct selected from the group consisting of sequesterants and cellulose-based material bleaching adjuncts.
- 3. A The composition of claim 1 further comprising a ligand L bound to the metal M.
- 4. The composition of claim 1 wherein the oxidant is a peroxy compound or ozone.
- 5. The composition of claim 4 wherein said peroxy compound is selected from the group consisting of hydrogen peroxide, hydrogen peroxide adducts, compounds capable of producing hydrogen peroxide in aqueous solution, organic peroxides, persulfates, perphosphates, and persilicates.
- 6. The composition of claim 1 wherein the oxidatively stable activator is a macrocyclic tetraamido metal-ligand complex having the structure: ##STR9## wherein X and Z may be H, electron donating or electron-withdrawing groups and R' and R" may be any combination of H, alkyl, cycloalkyl, cycloalkenyl, alkenyl, aryl, alkynyl, alkylaryl, halogen, alkoxy, or phenoxy substituents, or combine to form a cycyloalkyl or cycloalkenyl ring, which may contain at least one atom that is not carbon.
- 7. The composition of claim 6 wherein X and Z are independently selected from the group consisting of H, halogen, SO.sub.3, OSO.sub.3, OSO.sub.3 R (wherein R is H, alkyl, aryl, or alkylaryl) and NO.sub.2.
- 8. The composition of claim 6 wherein R' and R" are selected from H and C.sub.1-6 alkyl.
- 9. The composition of claim 6 wherein M is Fe or Mn.
- 10. The composition claim 6 wherein R' and R" are selected from H, CH.sub.3, CF.sub.3, halogen, or join together to form a cycloalkyl or cycloalkenyl, optionally with at least one atom which is not carbon.
- 11. The composition of claim 6 wherein X and Z are H.
- 12. A bleaching composition comprising:
- (a) an oxidatively stable activator having the structure ##STR10## wherein Y.sub.1, Y.sub.3 and Y.sub.4 each represents a bridging group having zero, one, two or three carbon containing nodes for substitution, and Y.sub.2 is a bridging group having at least one carbon containing node for substitution, each said node containing a C(R) or a C(R).sub.2 unit and each R substituent is the same or different from the remaining R substituents and (i) is selected from the group consisting of methyl, cycloalkyl, cycloalkenyl, alkenyl, aryl, alkynyl, alkylaryl, halogen, alkoxy, phenoxy, CH.sub.2 CF.sub.3, CF.sub.3 and combinations thereof, or (ii) form a substituted or unsubstituted benzene ring of which two carbon atoms in the ring form nodes in the Y unit, or (iii) together with a paired R substituent bound to the same carbon atom form a cycloalkyl or cycloalkenyl ring, which may include an atom other than carbon; M is a transition metal with oxidation states of I, II, III, IV, V, VI, VII or VIII or selected from Groups 3, 4, 5, 6, 7, 8, 9, 10, 11 and 12 of the Periodic Table of the Elements; and Q is any counterion which would balance the charge of the compound on a stoichiometric basis; and
- (b) an amount of a source of an oxidant effective for oxidizing products selected from the group consisting of chromophores, absorbable organic nonaromatic halogen species, and high molecular mass material species.
- 13. A bleaching composition comprising:
- (a) an oxidatively stable activator having the structure ##STR11## wherein Y.sub.1, Y.sub.3 and Y.sub.4 each represents a bridging group having zero, one, two or three carbon containing nodes for substitution, and Y.sub.2 is a bridging group having at least one carbon containing node for substitution, each said node containing a C(R) or a C(R).sub.2 unit and each R substituent is the same or different from the remaining R substituents and (i) is selected from the group consisting of methyl, cycloalkyl, cycloalkenyl, alkenyl, aryl, alkynyl, alkylaryl, halogen, alkoxy, phenoxy, CH.sub.2 CF.sub.3, CF.sub.3 and combinations thereof, or (ii) form a substituted or unsubstituted benzene ring of which two carbon atoms in the ring form nodes in the Y unit, or (iii) together with a paired R substituent bound to the same carbon atom form a cycloalkyl or cycloalkenyl ring, which may include an atom other than carbon; M is a transition metal with oxidation states of I, II, III, IV, V, VI, VII or VIII or selected from Groups 3, 4, 5, 6, 7, 8, 9, 10, 11 and 12 of the Periodic Table of the Elements; and Q is any counterion which would balance the charge of the compound on a stoichiometric basis; and
- (b) an amount of a source of an oxidant effective for oxidizing aromatic organic halogen species selected from the group consisting of chlorinated phenols, dioxins, dibenzoflurans, biphenyls and combinations thereof, or chlorinated lignin degradation products.
CROSS REFERENCE TO RELATED APPLICATION
This is a continuation in part of U.S. patent application Ser. No. 08/804,776, filed Feb. 24, 1997 now U.S. Pat. No. 5,853,428, which is a continuation in part of U.S. patent application Ser. No. 08/684,670, filed Jul. 22, 1996 now U.S Pat. No. 5,876,625.
STATEMENT REGARDING FEDERALLY SPONSORED RESEARCH
This work was supported by the National Science Foundation, grant CHE9319505, and the National Institute of Health, grant GM-44867. The United States government may have certain rights in this application.
US Referenced Citations (9)
Foreign Referenced Citations (1)
Number |
Date |
Country |
0 458 398 A2 |
Nov 1991 |
EPX |
Non-Patent Literature Citations (3)
Entry |
Terrence J. Collins, Designing Ligands For Oxidizing Complexes, Dept. Of Chem. Carnegie Mellon University, Accounts Of Chemical Reseach, (1994) 27, p. 279. |
Erich Stuart Uffelman, Macrocyclic Tetraamido-N-Ligands That Stabilize High Valent Complexes Of Chrominum, Maganese, Iron, Colbalt, Nickel, and Copper, California Institute Of Technology, (Aug. 19, 1991). |
Kimberely K. Kostka, Synthesis And Characterization Of high-Valent, Iron Complexes Of Macrocyclic Tetraamido-N-Ligands, Carnegie Mellon University, (Jul. 19, 1993). |
Continuation in Parts (2)
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Number |
Date |
Country |
Parent |
804776 |
Feb 1997 |
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Parent |
684670 |
Jul 1996 |
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