Anion-exchange resins including ion-exchange groups with at least two nitrogen groups, and methods of making and using same

• US 6,248,798 B1
• Filed: 11/23/1998
• Issued: 06/19/2001
• Est. Priority Date: 03/01/1996
• Status: Expired due to Term

• Current Assignee: Dionex Corporation (Thermo Fisher Scientific Incorporated)
• Original Assignee: Dionex Corporation (Thermo Fisher Scientific Incorporated)
• Inventors: Jagodzinski, Jacek J., Weitzhandler, Michael, Slingsby, Rosanne W., Narayanan, Latha P., Pohl, Christopher A.
• Primary Examiner(s): Zitomer, Fred
• Application Number:
  US09/198,203
• Time in Patent Office: 939 Days
• Field of Search: 521/28, 521/32, 521/25, 528/482, 210/661, 210/679, 210/692
• US Class Current: 521/28
• CPC Class Codes: B01D 15/363 Anion-exchange
• CPC Class Codes: B01J 41/05 in the strongly basic form
• CPC Class Codes: B01J 41/20 Anion exchangers for chromatographic processes
• CPC Class Codes: B01J 47/016 Modification or after-treatment of ion-exchangers

Abstract

Anion-exchange compositions are provided comprising anion-exchange functional groups comprising at least a first and a second nitrogen group, wherein the first nitrogen group is a quaternary amine and the second nitrogen group is selected from the group consisting of primary, secondary, tertiary or quaternary amines. Methods of making and using the compositions are also provided.

Claims

1. A chromatographic analytical column, the column containing a packed bed of an anion-exchange chromatographic packing and capable of quantitative chromatographic separation of carbohydrates, which column comprises:

a) Component A comprising support resin particles; and

b) polymers including polymerized functionalized monomers each containing anion-exchange functional groups, each anion-exchange functional group comprising at least a first and second nitrogen group, wherein said first nitrogen group is a quaternary amine of the formula X-NRR′

R″ and

said second nitrogen group is selected from the group consisting of a primary amine of the formula X-NH₂, a secondary amine of the formula X-NHR, a tertiary amine of the formula X-NRR′

or a quaternary amine of the formula X-NRR′

R″

wherein R, R′ and

R″

are straight or branched chained alkyl groups or cycloalkyl groups having from 1-10 carbons, and said polymers containing said anion-exchange functional groups are retained directly or indirectly on Component A.

4. The chromatographic analytical column of claim 1 in which said support resin particles contain at least about 30% crosslinking monomeric units.

5. The chromatographic analytical column of claim 1 where said support resin particles contain at least about 55% crosslinking monomeric units.

6. The chromatographic analytical column of claim 4 wherein said crosslinking monomeric units are divinylbenzene.

2. A chromatographic analytical column, the column containing a packed bed of an anion-exchange chromatographic packing capable of quantitative chromatographic separation of carbohydrates, which column comprises:

a) Component A comprising support resin particles; and

b) polymers containing anion-exchange functional groups, each anion-exchange functional group comprising at least a first and a second nitrogen group, wherein said first nitrogen group is a quaternary amine, and said second nitrogen group is selected from the group consisting of primary, secondary, tertiary or quaternary amines wherein said polymers are not substantially crosslinked through said anion functional groups;

wherein said polymers containing said anion-exchange functional groups are retained directly or indirectly on Component A.

3. A chromatographic analytical column, the column containing a packed bed of an anion-exchange chromatographic packing capable of quantitative chromatographic separation of carbohydrates, which column comprises:

a) Component A comprising support resin particles; and

b) polymers containing anion-exchange functional groups, each anion-exchange functional group comprising at least a first and a second nitrogen group, wherein said first nitrogen group is a quaternary amine, and said second nitrogen group is a tertiary amine;

wherein said polymers containing said anion-exchange functional groups are retained directly or indirectly on Component A.