The patent badge is an abbreviated version of the USPTO patent document. The patent badge does contain a link to the full patent document.
The patent badge is an abbreviated version of the USPTO patent document. The patent badge covers the following: Patent number, Date patent was issued, Date patent was filed, Title of the patent, Applicant, Inventor, Assignee, Attorney firm, Primary examiner, Assistant examiner, CPCs, and Abstract. The patent badge does contain a link to the full patent document (in Adobe Acrobat format, aka pdf). To download or print any patent click here.
Patent No.:
Date of Patent:
May. 11, 1976
Filed:
Sep. 04, 1974
Manuel Slovinsky, Woodridge, IL (US);
Joseph Matt, Chicago, IL (US);
Nalco Chemical Company, Oak Brook, IL (US);
Abstract
A series of microbicides which show 1- and 24-hour kill, 48-hour inhibition, and satisfactory simulated cooling tower inhibition against microorganisms such as bacteria, fungi, and algae prevalent in aqueous systems. The compounds are (2-hydroxy R) polyamines produced by reacting an R substituted alkylene oxide utilized in 1-2 mole quantities and reacted with a molar amount of an alkylene polyamine. The R substituent on the alkylene oxide is preferably alkyl where the chain length may be C.sub.6 -C.sub.20 as in epoxy alkanes, which may be straight or branched, saturated or unsaturated. The R substituent may also be aryl, aralkyl, or alkaryl, such as styrene oxide. The compounds are known as mono and bis (2-hydroxy R) polyamines depending upon whether 1 or 2 moles of the alkylene oxide are utilized. Protection in simulated cooling tower operation is achieved by dosages ranging as low as 1 ppm with an effective dosage range of 1-100 ppm. These compounds may be present as mixtures due to different points of possible attachment of the hydroxy R moiety to the amine, as, for example, in diethylene triamine, but the primary amine groups are favored for reaction. Additionally, these polyamine alcohols may be further modified by cyano- or haloethylation to introduce a cyanoethyl or haloethyl group at one or more of the remaining available nitrogens, and these products exhibit similar activity against microorganisms.