Hydrogen sulfide scavengers

Patent metadata

Field	Value
Publication number	US-9523045-B2
Application number	US-201414168594-A
Country	US
Kind code	B2
Filing date	Jan 30, 2014
Priority date	Jan 30, 2013
Publication date	Dec 20, 2016
Grant date	Dec 20, 2016

Abstract

Disclosed herein are scavenging compounds and compositions useful in applications relating to the production, transportation, storage, and separation of crude oil and natural gas. Also disclosed herein are methods of using the compounds and compositions as scavengers, particularly in applications relating to the production, transportation, storage, and separation of crude oil and natural gas.

First claim

What is claimed is:

1. A method of sweetening a fluid or gas, comprising treating the fluid or gas with an effective amount of a composition comprising one or more compounds of formula (I),

wherein
R 1 , R 2 , and R 3 are each independently selected from the group consisting of hydrogen, alkylenyl, alkenylenyl, alkynylenyl, alkyl, alkenyl, and alkynyl, wherein said alkylenyl, alkenylenyl, alkynylenyl, alkyl, alkenyl, and alkynyl are each independently, at each occurrence, substituted or unsubstituted with one or more suitable substituents;
k, l, and m are each independently an integer selected from the group consisting of 0 to 25, wherein k+l+m is >0; and
x, y, and z are each independently an integer selected from the group consisting of 0 and 1, wherein x+y+z is 1, 2, or 3;
provided that:
when x is 0, R 1 is hydrogen, alkyl, alkenyl, or alkynyl; and when x is 1, R 1 is alkylenyl, alkenylenyl, or alkynylenyl;
when y is 0, R 2 is hydrogen, alkyl, alkenyl, or alkynyl; and when y is 1, R 2 is alkylenyl, alkenylenyl, or alkynylenyl;
when z is 0, R 3 is hydrogen, alkyl, alkenyl, or alkynyl; and when z is 1, R 3 is alkylenyl, alkenylenyl, or alkynylenyl.

2. The method of claim 1 , wherein the compound of formula (I) has formula (II),

wherein
R 3 is selected from the group consisting of hydrogen, alkylenyl, alkenylenyl, alkynylenyl, alkyl, alkenyl, and alkynyl, wherein said alkylenyl, alkenylenyl, alkynylenyl, alkyl, alkenyl, and alkynyl are each independently substituted or unsubstituted with one or more suitable substituents;
k, l, and m are each independently an integer selected from the group consisting of 0 to 25, wherein k+l+m is >0; and
z is 0 or 1;
provided that:
when z is 1, R 3 is alkylenyl, alkenylenyl, or alkynylenyl;
when z is 0, R 3 is hydrogen, alkyl, alkenyl, or alkynyl.

3. The method of claim 1 , wherein the composition further comprises at least one compound selected from the group consisting of alkyl benzyl ammonium chloride, benzyl cocoalkyl(C 12 -C 18 )dimethylammonium chloride, dicocoalkyl(C 12 -C 18 )dimethylammonium chloride, ditallow dimethylammonium chloride, di(hydrogenated tallow alkyl)dimethyl quaternary ammonium methyl chloride, methyl bis(2-hydroxyethyl cocoalkyl(C 12 -C 18 )quaternary ammonium chloride, dimethyl(2-ethyl)tallow ammonium methyl sulfate, n-dodecylbenzyldimethylammonium chloride, n-octadecylbenzyldimethyl ammonium chloride, n-dodecyltrimethylammonium sulfate, soya alkyltrimethylammonium chloride, and hydrogenated tallow alkyl(2-ethylhyexyl)dimethyl quaternary ammonium methyl sulfate, or any combination thereof.

Assignees

• Ecolab Usa Inc

Inventors

• Harrington Ryan Matthew
• Anantaneni Prakasa Rao
• Karas Lawrence J
• Ekoue-Kovi Kekeli

Classifications

• B01D2252/20489

  with two or more hydroxyl groups · CPC title

• B01D2252/20426

  Secondary amines · CPC title

• B01D53/1468

  Removing hydrogen sulfide · CPC title

• C07C217/08 Primary

  the oxygen atom of the etherified hydroxy group being further bound to an acyclic carbon atom · CPC title

• C10L2230/02

  Absorbents, e.g. in the absence of an actual absorbent column or scavenger · CPC title