US 4,816,508 AGrant
Stabilized Cationic Acrylate or Methacrylate Polymer Admixtures
Issue Date:1989-03-28
•3 Claims
Abstract
The present invention is directed to an admixture, comprising: The present invention is also directed to a method for improving the stability of cationic acrylate polymers, comprising adding 0.1 to 5.0%, by weight, based on the weight of the polymer, of an acidic buffering compound. (A) a cationic acrylate or methacrylate polymer and (B) 0.1 to 5.0%, by weight, based on the weight of said polymer, of an acidic buffering compound.
Metadata
Assignee
- Calgon Corporation
Inventor
- Shih-Ruey T. Chen
Application Information
Application Number:US 1830244
Filing Date:1988-04-18
Priority Date:1985-11-07
Art Unit:155
Classifications
IPC:
C08K 509
Field of Search:
524300;321
Patent Drawings
This patent does not have any drawings.
Description
Background of the Invention
The storage life of cationic acrylate polymers, particularly emulsions, is short due to the lack of hydrolytic stability. These polymers are also found to degrade during dilution, especially in a neutral or high pH aqueous solution. A long storage life and good hydrolytic stability is desired to maintain the product quality, i.e. activity.
It was surprisingly found that acidic buffering compounds improve the stability of these polymers.
Description of the Invention
The present invention is directed to an admixture, comprising:
(A) a cationic acrylate polymer and
(B) 0.1 to 5.0%, by weight, based on the weight of said polymer, of an acidic buffering compound.
The present invention is also directed to a method for improving the stability of cationic acrylate polymers, comprising adding 0.1 to 5.0%, by weight, based on the weight of the polymer, of an acidic buffering compound.
Any cationic acrylate polymer's stability is enhanced by the addition of an acidic buffering compound. The word "acrylate" is defined herein to include methacrylate. Specific examples of cationic acrylate polymers include homopolymers of methacryloyloxyethyl trimethyl ammonium methosulfate (METAMS), methacryloyloxyethyl trimethyl ammonium chloride (METAC), acryloyloxyethyl trimethyl ammonium chloride (AETAC), and copolymers of the above monomers with acrylamide. The preferred polymers are copolymers of acrylamide and 2-methacryloyloxyethyl trimethyl ammonium chloride (AM/METAC) and copolymers of acrylamide and methacryloyloxyethyl trimethyl ammonium methosulfate (AM/METAMS).
Although any cationic polymer's stability may be enhanced by the addition of the acid buffer, those having an intrinsic viscosity of at least 2.0 (MWT greater than 1,000,000) in 1.0M sodium chloride are more prone to stability problems.
Any acidic buffering compound may be used. The preferred acidic buffering compounds are carboxylic acids with a pK.sub.1 of 1.19 to 3.08 and a pK.sub.2 of 4.72 to 13.0. Examples include citric acid, phthalic acid, succinic acid, adipic acid, tartaric acid and malic acid. The most preferred acidic buffering compound is citric acid.
The acidic buffering agent is used in a dosage range of 0.1 to 5.0%, by weight, based on the weight of the polymer.
The stability of the polymer is enhanced in all forms, e.g. emulsion, solution, and dry.
The admixtures of the present invention may be used as dewatering and paper retention aids.
Examples 1 Through 8
A set of water-in-oil emulsion copolymers of acrylamide and 2-methacryloyloxyethyl trimethyl ammonium chloride (40/60 w/w, 37.5% active) was prepared. After polymerization, a citric acid solution was slowly added in before addition of the inverting surfactant. This set of emulsions, containing differing levels of citric acid, was stored at both 50.degree. C. and room temperature for four weeks. The polymer reduced viscosity (0.05% in 1N NaCl at 30.degree. C.), the net cationic unit on the polymer, and the polymer performance as a sludge dewatering aid, were compared to a control. The results are shown in Table I below.
Examples 9 Through 11
A commercial AM/METAMS dry polymer (Calgon K-400) was blended with both 2.5% and 4.0% citric acid (anhydrous). Next, these polymer blends, as well as the original polymer, were dissolved in tap water to make a 0.1% solution. The % net cationic unit (as METAMS) on polymer was determined initially and after 24 hours. The polymers with citric acid were stable. The results are summarized in Table II.
Example 12
The emulsion polymers of Example 1 through 8 were diluted down to 0.1% concentration in three different industrial waters. The polymers with citric acid were more stable than the one without citric acid as indicated in Table III.
Claims
What is claimed is:
1. A method for improving the stability of a cationic water-in-oil polymer emulsion comprising adding 0.1 to 5%, by weight, based on the weight of said polymer in said emulsion, of a carboxylic acid having a pK.sub.1 of 1.9 to 3.08 and a pK.sub.2 of 4.2 to 13.0 to said emulsion after polymerization and before addition of an inverting surfactant; wherein said polymer is selected from the group consisting of polymers prepared using methacryloyloxyethyl trimethyl ammonium methosulfate, methacryloyloxyethyl trimethyl ammonium chloride or acryloyloxyethyl trimethyl ammonium chloride, alone or in combination with acrylamide.
2. The method of claim 1, wherein said polycarboxylic acid is selected from the group consisting of citric acid, phthalic acid, succinic acid, adipic acid, tartaric acid and maleic acid.
3. The method of claim 2, wherein said polycarboxylic acid is citric acid.