Use of heterocyclic compounds as activators for inorganic peroxy

Compositions – Oxidative bleachant – oxidant containing – or generative – Contains activator admixed with inorganic peroxide

Patent

Rate now

  [ 0.00 ] – not rated yet Voters 0   Comments 0

Details

2521864, 423584, 540451, 540454, 540488, 540524, 540525, 544 96, 544 97, 546188, 546189, 546207, 546208, 548230, 548524, 548551, 549266, 549291, 549292, 549295, 549320, 549322, C11D 339, A61L 218

Patent

active

059722371

DESCRIPTION:

BRIEF SUMMARY
BACKGROUND OF THE INVENTION

1. Field of the Invention
The present invention relates to the use of certain heterocyclic compounds based on cyclic carbamates, lactones or lactams as activators for inorganic peroxy compounds, in particular as cold bleach activators or optical brighteners in detergents, cleaners and bleaches and in disinfectants. The present invention furthermore relates to certain industrial formulations which contain these heterocyclic compounds.
2. Description of the Background
In the efforts to achieve energy-saving washing, cleaning and bleaching processes, recently use temperatures in the lower temperature range have become increasingly important, for example for textile laundering distinctly below 60.degree. C., and in particular below 45.degree. C. However, at these temperatures, the effect of the known activators for inorganic peroxy compounds, this being the system responsible for the bleaching or cleaning action, decreases markedly. There has thus been no lack of attempts to develop more effective activators for this temperature range, without any convincing success to date.
EP-A 028 432 discloses textile detergent formulations which contain, among other things, N-acyllactams, eg. N-acetylcaprolactam, as precursor for a bleaching organic peroxy acid.


SUMMARY OF THE INVENTION

It is an object of the present invention to improve the bleaching, oxidizing and cleaning action of a system comprising activator and inorganic peroxy compounds in the lower temperature range, in particular from 15 to 60.degree. C.
We have found that this object is achieved by using heterocyclic compounds of the general formula I ##STR2## (b) a lactonoxy residue of the formula ##STR3## or (c) a lactam residue of the formula ##STR4## where Z.sup.1 to Z.sup.3 are 1,2-, 1,3-, 1,4- or 1,5-alkylene groups which have 2 to 20 carbon atoms and which can additionally be functionalized by one to three hydroxyl groups, C.sub.1 -C.sub.4 -alkoxy groups, amino groups, C.sub.1 -C.sub.4 -alkylamino groups, di-C.sub.1 -C.sub.4 -alkylamino groups, chlorine atoms, bromine atoms, nitro groups, cyano groups, carboxyl groups, sulfo groups, carboxy-C.sub.1 -C.sub.4 -alkyl groups, carboxamide groups or phenyl, tolyl or benzyl radicals, it being possible for aromatic nuclei in turn likewise to be substituted by the said radicals, or can be interrupted by one or two non-adjacent oxygen atoms, amino groups, C.sub.1 -C.sub.4 -alkylamino groups or carbonyl groups, and ##STR5## where Y is hydrogen, ammonium which may be substituted by organic radicals, or C.sub.1 -C.sub.4 -alkyl, and group, a C.sub.5 -C.sub.32 -cycloalkylene group, a C.sub.7 -C.sub.30 -aralkylene group,. a C.sub.6 -C.sub.18 -arylene group or a C.sub.3 -C.sub.18 -hetarylene group, it being possible for aliphatic structural units additionally to be functionalized by one to five hydroxyl groups, C.sub.1 -C.sub.4 -alkoxy groups, amino groups, C.sub.1 -C.sub.4 -alkylamino groups, di-C.sub.1 -C.sub.4 -alkylamino groups, chlorine atoms, bromine atoms, nitro groups, cyano groups, carboxyl groups, sulfo groups, carboxy-C.sub.1 -C.sub.4 -alkyl groups, carboxamide groups or phenyl, tolyl or benzyl radicals, where aromatic, cycloaliphatic and heteroaromatic structural units can likewise be substituted by the said radicals, or to be interrupted by one to eight non-adjacent oxygen atoms, amino groups, C.sub.1 -C.sub.4 -alkylamino groups or carbonyl groups, and residue (b), of a lactam residue (c) in which the group Z.sup.3 is a 1,2-, 1,3- or 1,5-alkylene group which has 2 to 20 carbon atoms, and which can additionally be functionalized or interrupted by the radicals or atoms indicated above, and of a lactam residue (c) in which the group Z.sup.3 is a 1,4-alkylene group which has 4 to 20 carbon atoms and which can likewise additionally be functionalized or interrupted by the radicals or atoms indicated above, and in which, at the same time, the group X connected thereto is --SO--, --SO.sub.2 --, --PO(OY)--, --CO--CO-- or --CO--A--CO--, has the following meaning: -cycloalkyl, C.sub.7 -C

REFERENCES:
CA 120: 106829, 1993.
CA 121: 17822, 1993.
CA 111: 115118, 1989.
CA 98: 160816, 1982.

LandOfFree

Say what you really think

Search LandOfFree.com for the USA inventors and patents. Rate them and share your experience with other people.

Rating

Use of heterocyclic compounds as activators for inorganic peroxy does not yet have a rating. At this time, there are no reviews or comments for this patent.

If you have personal experience with Use of heterocyclic compounds as activators for inorganic peroxy, we encourage you to share that experience with our LandOfFree.com community. Your opinion is very important and Use of heterocyclic compounds as activators for inorganic peroxy will most certainly appreciate the feedback.

Rate now

     

Profile ID: LFUS-PAI-O-760048

  Search
All data on this website is collected from public sources. Our data reflects the most accurate information available at the time of publication.