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Title:
MICROBIAL-RESISTANT DISPERSANT
Document Type and Number:
WIPO Patent Application WO/2024/006644
Kind Code:
A1
Abstract:
The present invention relates to a composition comprising water, a carboxylic acid functionalized dispersant and a compound of Formula (I) : where R, R1, x, and y are as defined herein. The composition of the present invention is useful as a biocide-free additive for pre-paint formulations.

Inventors:
FRANKEL ERICA A (US)
CONLEY TARA L (US)
Application Number:
PCT/US2023/068765
Publication Date:
January 04, 2024
Filing Date:
June 21, 2023
Export Citation:
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Assignee:
ROHM & HAAS (US)
International Classes:
C09D7/45; A01N25/04; A01N25/30; A01P1/00; A01P3/00; C09D7/63; C09D7/65
Domestic Patent References:
WO2022031444A12022-02-10
Foreign References:
US20170088713A12017-03-30
EP3403505A12018-11-21
US20130217780A12013-08-22
US4670167A1987-06-02
US20070048345A12007-03-01
Attorney, Agent or Firm:
WILLIS, Reid (US)
Download PDF:
Claims:
Claims: 1. A composition comprising, based on the weight of the composition, a) from 50 to 90 weight percent water, b) from 9 to 45 weight percent of a carboxylic acid functionalized dispersant; c) and from 0.5 to 10 weight percent of a compound of Formula I: wherein each R is independently H, methyl, or ethyl; R1 = –R2-NR3-(CH2CH2O)z-H; or –C6-C18-alkyl; or –C(CH3)2R4; x is from 1 to 40; y is from 0 to 39; and z is from 0 to 39; with the proviso that when y is 0, R1 is –C(CH3)2R4; and when y is from 1 to 39, R1 is –R2-NR3-(CH2CH2O)y-H or –F-alkyl; R2 is –CH2CH2CH2– or –CH(CH3)CH2– or –CH2CH(CH3)–; R3 is saturated or partially unsaturated C10-C22-alkyl; R4 is C1-C20-alkyl; and x + y + z = 1 to 40; wherein at least 80 weight percent of the composition comprises water, the dispersant, and the compound for Formula I; and wherein the composition has a pH in the range of from 8 to 11. 2. The composition of Claim 1 which has a pH in the range of from 8.5 to 10 wherein, based on the weight of the composition, the concentration of water is in the range of from 55 to 85 weight percent; the concentration of the carboxylic acid functionalized dispersant is in the range of from 15 to 45 weight percent; and the concentration of the compound of Formula I is in the range of from 1.5 to 8 weight percent.

3. The composition of Claim 2 wherein the compound of Formula I is represented by the compound of Formula Ia: where R4 is C6-C14-alkyl, and x = 2 to 30; or the compound of Formula Ib: where R3 is a saturated or partially saturated C14 C20 alkyl, or saturated or partially saturated C16-C18-alkyl, and x + y + z = 2 to 32; or the compound of Formula Ic: where R1 is C12-C18-alkyl, and x + y = 12 to 18.

4. The composition of Claim 3 wherein the compound of Formula I is represented by the compound of Formula Ia: where R4 is decyl and x = 2 to 10. 5. The composition of either of Claims 3 or 4 wherein the weight-to-weight ratio of the carboxylic acid functionalized dispersant to the compound of Formula Ia is in the range of from 5:1 to 10:1; wherein the composition further includes 2-amino-2-methyl-1-propanol. 6. The composition of any of Claims 1 to 4 wherein the carboxylic acid functionalized dispersant is selected from the group consisting of a homopolymer of acrylic acid, a homopolymer of methacrylic acid, a copolymer of acrylic acid and methacrylic acid, a copolymer of acrylic acid and hydroxypropyl acrylate, a copolymer of acrylic acid and hydroxyethyl methacrylate, a copolymer of methacrylic acid and hydroxypropyl acrylate, a copolymer of methacrylic acid and hydroxyethyl methacrylate, and a copolymer of maleic anhydride and diisobutylene; wherein the composition further includes 2-amino-2-methyl-1- propanol. 7. The composition of Claim 6 wherein the carboxylic acid functionalized dispersant is selected from the group consisting of a homopolymer of acrylic acid, a copolymer of methacrylic acid and hydroxypropyl acrylate, and a copolymer of maleic anhydride and diisobutylene. 8. The composition of any of Claims 1 to 7 which further comprises, based on the weight of the composition, from 1 to 20 weight percent of a nonionic ethoxylated C6-C12 alcohol, or a nonionic propoxylated C6-C12 alcohol or a nonionic ethoxylated-propoxylated C6-C12 alcohol.

Description:
Microbial-Resistant Dispersant Background of the Invention The present invention relates to a microbial-resistant dispersant, more particularly, a dispersant that has preservative properties in the absence of a biocide. Isothiazolinones are commonly used as preservatives in a wide variety of consumer products including architectural coatings. However, isothiazolinones are known skin sensitizers and have come under increased scrutiny by regulators for use in a variety of consumer products. In 2016, the European Commission issued a directive to limit the use of methylisothiazolinone (MIT) in most consumer products, including house paint. By 2021, the EU decided that it would not permit final formulations of these products to contain more than 15 ppm of MIT. These stringent restrictions present a challenge for paint formulators looking to control the amount of biocide in their final product. It would therefore be an advance in the art of architectural coatings to discover a biocide-free solution for preserving additives used in paint formulations. Summary of the Invention The present invention addresses a need in the art by providing composition comprising, based on the weight of the composition, a) from 50 to 90 weight percent water, b) from 9 to 45 weight percent of a carboxylic acid functionalized dispersant; c) and from 0.5 to 10 weight percent of a compound of Formula I: I wherein each R is independently H, methyl, or ethyl; R 1 = –R 2 -NR 3 -(CH2CH2O)z-H; or –C6-C18-alkyl; or –C(CH3)2R 4 ; x is from 1 to 40; y is from 0 to 39; and z is from 0 to 39; with the proviso that when y is 0, R 1 is –C(CH3)2R 4 ; and when y is from 1 to 39, R 1 is –R 2 -NR 3 -(CH 2 CH 2 O) y -H or –C 6 -C 18 -alkyl; R 2 is –CH2CH2CH2– or –CH(CH3)CH2– or –CH2CH(CH3)–; R 3 is saturated or partially unsaturated C10-C22-alkyl; R 4 is C1-C20-alkyl; and x + y + z = 1 to 40; wherein at least 80 weight percent of the composition comprises water, the dispersant, and the compound for Formula I; and wherein the composition has a pH in the range of from 8 to 11. The composition of the present invention is useful as a biocide-free additive for paint or pre-paint formulations. Detailed Description of the Invention The present invention is a composition comprising, based on the weight of the composition, a) from 50 to 90 weight percent water, b) from 9 to 45 weight percent of a carboxylic acid functionalized dispersant; c) and from 0.5 to 10 weight percent of a compound of Formula I: I wherein each R is independently H, methyl, or ethyl; R 1 = –R 2 -NR 3 -(CH2CH2O)z-H; or –C6-C18-alkyl; or –C(CH3)2R 4 ; x is from 1 to 40; y is from 0 to 39; and z is from 0 to 39; with the proviso that when y is 0, R 1 is –C(CH3)2R 4 ; and when y is from 1 to 39, R 1 is –R 2 -NR 3 -(CH2CH2O)y-H or –C6-C18-alkyl; R 2 is –CH2CH2CH2– or –CH(CH3)CH2– or –CH2CH(CH3)–; R 3 is saturated or partially unsaturated C10-C22-alkyl; R 4 is C1-C20-alkyl; and x + y + z = 1 to 40; wherein at least 80 weight percent of the composition comprises water, the dispersant, and the compound for Formula I; and wherein the composition has a pH in the range of from 8 to 11. The term carboxylic acid functionalized dispersant refers to a polymer functionalized with COO-X + groups, where X is a counterion such as sodium, potassium, or ammonium. Examples of suitable dispersants include acrylic acid (AA) homopolymers, methacrylic acid (MAA) homopolymers, copolymers of AA and MAA, copolymers of AA or MAA and an acrylate or methacrylate monomer such as hydroxypropyl acrylate (HPA) or hydroxyethyl methacrylate (HEMA), copolymers of maleic anhydride (MA) and diisobutylene (DIB). A dispersant prepared from maleic anhydride becomes carboxylic acid functionalized because the maleic anhydride groups hydrolyze to carboxylate groups in the presence of a base. The concentration of the carboxylic acid functionalized dispersant, based on the weight of the composition, is in the range of from 9 or from 15 or from 18 weight percent, to 45 or to 42 weight percent. The concentration of water is in the range of from 50 or from 55 weight percent, to 90 or to 85 weight percent. The concentration of the compound of Formula I, based on the weight of the composition, is in the range of from 0.5 or from 1 or from 1.5 or from 2 weight percent to 10 or to 8 or to 6 weight percent. Where y is 0, the compound of Formula I is represented by Formula Ia: where R 4 is preferably C6-C14-alkyl, and x = 2 to 30, or 10, or to 5. Examples of commercial surfactants within the scope of Formula Ia include TRITON™ RW-20 (RW-20, x = 2, R 4 = decyl), TRITON™ RW-50 (RW-50, x = 5, R 4 = decyl), and TRITON™ RW-150 (RW-150, x = 15, R 4 = decyl) Surfactants. (TRITON is a Trademark of The Dow Chemical Company or its Affiliates.) Another subgenus of the compound of Formula I is represented by Formula Ib: where R 3 is preferably saturated or partially saturated C14-C20-alkyl, or saturated or partially saturated C 16 -C 18 -alkyl, and x + y + z = 2 to 32. As used herein, “partially unsaturated” refers to the presence of one or two double bond within the alkyl chain. Examples of commercial surfactants within the scope of Formula Ib include Ethox DT-15 (DT-15, x + y + z = 15); and Ethox DT-30 (DT-30, x + y + z = 30) Tallow diamines. Yet another subgenus of the surfactant of Formula I is illustrated by Formula Ic: where R 1 is preferably C12-C18-alkyl, and x + y = 12 to 18. An example of a commercial surfactant within the scope of Formula Ic is Ethox CAM-15 Cocoamine (CAM-15, x + y = 15). The weight-to-weight ratio of the dispersant to a compound of Formula I is typically in the range of from 5:1 to 10:1. The pH of the composition is in the range of from 8, or from 8.5, to 11 or to 10 or to 9.5. The desired pH is conveniently achieved by addition of a neutralizer, which is preferably an amine such as 2-amino-2-methyl-1-propanol. The composition may further comprise an ancillary surfactant such as a nonionic ethoxylated and/or propoxylated C6-C12 alcohol or C8-C12 alcohol. The concentration of the ancillary surfactant, if used, is generally in the range of from 1 to 20 weight percent, based on the weight of the composition. A commercially available ancillary surfactant is TRITON™ DF-16 nonionic surfactant (DF-16). The composition of the present invention may be admixed with a pre-paint additive such as TiO 2 to impart preservative properties to the pre-paint. Examples Preparation of compositions Solutions of dispersant were placed in 50-mL conical tubes and vortexed with surfactant and sufficient AMP-952-amino-2-methyl-1-propanol neutralizer to achieve a final pH of ~9.5. Table 1 illustrates the relative proportions of the Dispersant; Surfactant I (RW-20, which is a compound within the scope of Formula I); Surfactant II (DF-16 which is used in example 4 only). 1124 refers to TAMOL™ 1124 Dispersant (a copolymer of AA and HPA); 165A refers to TAMOL™ 165A Dispersant (a copolymer of MA and DIB); and 851 refers to TAMOL™ 851 Dispersant (AA homopolymer). Table 1 illustrates the make-up of the dispersant compositions. The weight %s of water in each sample is the difference between 100 and the sum of the dispersant and the surfactant. Table 1 – Dispersant Compositions Ex. Dispersant Surfactant I Surfactant II No. Dispersant Surfactant I Surfactant II (wt%) (wt%) (wt%) 1 1124 RW-20 - 40 5 - 2 165A RW-20 - 20 2.5 - 3 851 RW-20 - 25 3.1 - 4 1124 RW-20 DF-16 35 5 20

Preparation of Samples for Microbial Resistance of TiO2 Four samples were prepared by adding each of the dispersant compositions of Examples 1-4 with Kronos 2311 TiO 2 slurry to a speedmixer (Flaktek, Inc.) with mixing at 1500 rpm for 2 min. A comparative Dispersant Blend was prepared by combining a sample that did not contain RW-20 with the TiO 2 slurry. Table 2 illustrates the make-up of the modified TiO 2 slurry compositions. Kronos 2311 TiO2 Slurry was used as the opacifying pigment for each study. Composition refers to the dispersant compositions of Examples 1-4. Table 2 – TiO2 Slurry Compositions Sample Ex. No. TiO2 (g) Composition (g) Water (g) 1 Ex.1 76.5 0.50 23.0 2 Ex.2 76.5 1.00 22.5 3 Ex.3 76.5 0.80 22.7 4 Ex.4 76.5 0.57 22.9 The concentration of dispersant in each sample was 0.2 weight percent, based on the weight of the sample. The dispersant compositions and the slurry compositions were inoculated 3 times at 7-d intervals with 10 6 -10 7 colony forming units per milliliter of sample (CFU/mL) of a standard pool of bacteria, yeasts, and molds obtained from American Type Culture Collection (ATCC) that are common contaminants in coatings. Once inoculated, the samples were stored in 25 ºC incubators. Test samples were monitored for microbial contamination by agar plating using a standard streak plate method. Samples were plated 1 d and 7 d after each microbial challenge onto trypticase soy agar (TSA) and potato dextrose agar (PDA) plates. All agar plates were checked daily up to 7 d after plating to determine the number of microorganisms surviving in the test samples. When not being checked, the agar plates were stored in incubators, 30 ºC for TSA plates and 25 ºC for PDA plates. The extent of microbial contamination was established by counting the colonies, where the rating score was determined from the number of microbial colonies observed on the agar plates. Reported results come from day 7 readings. Results are described by the rating score for each type of microorganism: B = bacteria, Y = yeast, and M = mold. For example, a 3B describes a plate with 3 rating score for bacteria, or a Tr Y(1) describes a plate with trace yeast (1 colony on plate). Table 1 illustrates the rating system used to estimate the level of microbial contamination on streak plates. Colonies refers to the number of colonies on the plate. Table 3 illustrates the rating system estimating microbial contamination. Table 3 – Rating system for estimating microbial contamination Colonies Rating Score Contamination Result None 0 None Pass 1-9 Tr Trace Pass 10 to 99 1 Very Light Fail 100 to ~1000 2 Light Fail ~1000 to 10,000 3 Moderate Fail >10,000 4 Heavy Fail Table 4 illustrates the results of three challenge tests (C1 – C3) for the dispersant compositions. Table 4 – Challenge Test Results for Dispersant Compositions Ex. No. C1 Final C2 Final C3 Final 1 PASS PASS PASS 2 PASS PASS PASS 3 PASS PASS PASS 4 PASS PASS PASS In contrast, the copolymer of AA and HPA and the homopolymer of AA that did not contain the RW-20 amine ethoxylate surfactant failed all three challenge tests. Table 5 illustrates the three challenge tests for the TiO2 slurry compositions. Comparative Sample 1 (Comp.1) was prepared without RW-20.

Table 5 – Challenge Test Results for TiO2 Slurry Compositions Sample TiO 2 Dispersant Blend C1 Final C2 Final C3 Final Comp.1 Kronos 2311 no RW-20 FAIL FAIL FAIL 1 Kronos 2311 1 PASS PASS PASS 2 Kronos 2311 2 PASS PASS PASS 3 Kronos 2311 3 PASS PASS PASS 4 Kronos 2311 4 PASS PASS PASS The results show the efficacy of the dispersant composition beyond preservation of the composition itself. It is believed that the dispersant composition would be useful in improvement the preservation of other additives used in paint formulations.