Polymer with branched structure
11479688 · 2022-10-25
Assignee
Inventors
Cpc classification
C09D133/08
CHEMISTRY; METALLURGY
C08F220/286
CHEMISTRY; METALLURGY
C08L33/14
CHEMISTRY; METALLURGY
C08F220/14
CHEMISTRY; METALLURGY
C08F220/1802
CHEMISTRY; METALLURGY
C08F220/1802
CHEMISTRY; METALLURGY
C08F220/286
CHEMISTRY; METALLURGY
C08F220/06
CHEMISTRY; METALLURGY
C09D133/08
CHEMISTRY; METALLURGY
C08L33/14
CHEMISTRY; METALLURGY
C08F220/14
CHEMISTRY; METALLURGY
C08F220/06
CHEMISTRY; METALLURGY
International classification
C08F220/26
CHEMISTRY; METALLURGY
C09D133/08
CHEMISTRY; METALLURGY
C08F220/14
CHEMISTRY; METALLURGY
C08F220/06
CHEMISTRY; METALLURGY
Abstract
The presently claimed invention relates to polymer with branched structure, in particular, hydrophobically modified alkali-soluble (or alkali-swellable) emulsion (HASE) copolymers which are effective thickeners at high shear rates and at the same time offer a Newtonian rheology profile and their use in aqueous compositions, particularly in aqueous coating formulations as well as a method for preparing hydrophobically modified alkali-soluble (or alkali-swellable) emulsion copolymers.
Claims
1. A copolymer which is obtained by reacting a mixture comprising: (A) ≥30 wt.-% to ≤70 wt.-% of at least one ethylenically unsaturated monomer with a carboxylic function, (B) ≥30 wt.-% to ≤70 wt.-% of at least one non-ionic ethylenically unsaturated monomer, (C) ≥1 wt.-% to ≤40 wt.-% of at least one monomer of formula (I) ##STR00009## wherein R.sub.1 denotes hydrogen or methyl, n is a real number in the range of ≥10 to ≤80, and R.sub.2 denotes branched, unsubstituted C.sub.10-C.sub.15 alkyl, (D) ≥0 wt.-% to ≤1 wt.-% of at least one crosslinking reagent, (E) ≥0 wt.-% to ≤10 wt.-% of at least one ethylenically unsaturated monomer which is different from (A), (B), and (C), and (F) ≥0 wt.-% to ≤1 wt.-% of at least one chain transfer agent, wherein wt.-% is based on the total weight of the mixture, and wherein the C.sub.10-C.sub.15 alkyl has a mean degree of branching (iso-index) in the range of ≥1.5 to ≤3.5.
2. The copolymer according to claim 1, wherein the C.sub.10-C.sub.15 alkyl has a mean degree of branching (iso-index) in the range of ≥1.8 to ≤2.8.
3. The copolymer according to claim 1, wherein the C.sub.10-C.sub.15 alkyl has a mean degree of branching (iso-index) in the range of ≥2 to ≤2.5.
4. The copolymer according to claim 1, wherein R.sub.2, denotes branched, unsubstituted C.sub.12-C.sub.15 alkyl.
5. The copolymer according to claim 4, wherein the C.sub.12-C.sub.15 alkyl has a mean degree of branching (iso-index) in the range of ≥1.8 to ≤2.8.
6. The copolymer according to claim 4, wherein the C.sub.12-C.sub.15 alkyl has a mean degree of branching (iso-index) in the range of ≥2 to ≤2.5.
7. The copolymer according to claim 1, wherein R.sub.1 denotes methyl.
8. The copolymer according to claim 1, wherein the at least one ethylenically unsaturated monomer with a carboxylic function (A) is provided in an amount of 33 wt.-% to ≤67 wt.-%.
9. The copolymer according to claim 1, wherein the at least one ethylenically unsaturated monomer with a carboxylic function (A) is provided in an amount of 36 wt.-% to ≤64 wt.-%.
10. The copolymer according to claim 1, wherein the at least one non-ionic ethylenically unsaturated monomer (B) is provided in an amount of ≥33 wt.-% to ≤67 wt.-%.
11. The copolymer according to claim 1, wherein the at least one non-ionic ethylenically unsaturated monomer (B) is provided in an amount of ≥40 wt.-% to ≤60 wt.-%.
12. The copolymer according to claim 1, wherein the at least one non-ionic ethylenically unsaturated monomer (B) is a mixture of at least two different non-ionic ethylenically unsaturated monomers (B).
13. The copolymer according to claim 12, wherein the at least two different non-ionic ethylenically unsaturated monomers (B) are provided in an amount of ≥33 wt.-% to ≤67 wt.-%.
14. The copolymer according to claim 12, wherein the at least two different non-ionic ethylenically unsaturated monomers (B) are provided in an amount of ≥40 wt.-% to ≤60 wt.-%.
15. The copolymer according to claim 1, wherein the at least one monomer (C) is a mixture of at least two different monomers of formula (I).
16. The copolymer according to claim 1, wherein the at least one monomer (C) of formula (I) is provided in an amount of ≥8 wt.-% to ≤30 wt.-%.
17. The copolymer according to claim 1, wherein the at least one monomer (C) of formula (I) is provided in an amount of ≥8 wt.-% to ≤20 wt.-%.
18. The copolymer according to claim 1, wherein the at least one cross linking reagent (D) is provided in an amount of ≥0 wt.-% to ≤0.5 wt.-%.
19. The copolymer according to claim 1, wherein the at least one monomer (E) is provided in an amount of ≥0 wt.-% to ≤5 wt.-%.
20. The copolymer according to claim 1, wherein the at least one chain transfer agent (F) is provided in an amount of ≥0 wt.-% to ≤0.5 wt.-%.
21. The copolymer according to claim 1, wherein the at least one ethylenically unsaturated monomer with a carboxylic function (A) is selected from the group consisting of acrylic acid, methacrylic acid, C.sub.1 to C.sub.4 monoesters of maleic or itaconic acids, and mixtures thereof, or is selected from the group consisting of ethylenically unsaturated monomer with a carboxylic function, consisting of crotonic, isocrotonic, cinnamic, itaconic, maleic acid, and maleic anhydride.
22. The copolymer according to claim 1, wherein the at least one ethylenically unsaturated monomer with a carboxylic function (A) is selected from the group consisting of acrylic acid, methacrylic acid, C.sub.1 to C.sub.4 monoesters of maleic or itaconic acids, and mixtures thereof.
23. The copolymer according to claim 1, the at least one non-ionic ethylenically unsaturated monomer (B) is selected from the group consisting of methyl, ethyl, butyl or 2-ethyl-hexyl esters of acrylic and methacrylic acid.
24. The copolymer according to claim 1, wherein in the at least one monomer (C) of formula (I) R.sub.1; is a methyl and n is a real number in the range of ≥10 to ≤60.
25. The copolymer according to claim 1, wherein in the at least one monomer (C) of formula (I) R.sub.1 is a methyl and n is a real number in the range of ≥10 to ≤50.
26. The copolymer according to claim 1, wherein the at least one crosslinking reagent (D) is selected from the group consisting of ethylene glycol diacrylate; ethylene glycol dimethacrylate; trimethylolpropanetriacrylate; trimethylolpropanetrimethacrylate; allyl acrylate; methylenebisacrylamide; methylenebismethacrylamide; tetrallyloxyethane; triallylcyanurates; allylic ethers of pentaerythritol, sorbitol, or sucrose; and a diallylester of phthalic acid.
27. The copolymer according to claim 1, wherein at least one ethylenically unsaturated monomer (E) is selected from the group consisting of linear, branched, cycloaliphatic or arylaliphatic esters of acrylic or methacrylic acids; isomers of butyl (meth)acrylate; isomers of hexyl (meth)acrylate; n-octyl (meth)acrylate; 2-ethylhexyl (meth)acrylate; 1-decyl (meth)acrylate; 2-decyl (meth)acrylate; isodecyl (meth)acrylate; isomers of dodecyl (meth)acrylate, cyclohexyl (meth)acrylate, isobornyl (meth)acrylate or benzyl (meth)acrylate; vinylaromatic monomers and amide or nitrile derivatives of (meth)acrylic acids.
28. The copolymer according to claim 1, wherein at least one chain transfer agent (F) is selected from the group consisting of n-dodecyl mercaptan; n-decyl mercaptan; octyl mercaptan; 1,8-dimercapto-3,6-dioxaoctane; thiolactic acid; tert-dodecanthiol; 2-(ethylhexyl)thioglycolate; and terpinolene.
29. The copolymer according to claim 1, which is obtained by reacting a mixture comprising: (A) ≥30 wt.-% to ≤70 wt.-% of at least one ethylenically unsaturated monomer with a carboxylic function selected from the group consisting of acrylic acid; methacrylic acid; C.sub.1 to C.sub.4 monoesters of maleic or itaconic acids, and mixtures thereof; and ethylenically unsaturated monomer with a carboxylic function, consisting of crotonic, isocrotonic, cinnamic, itaconic, maleic acid, and maleic anhydride, (B) ≥30 wt.-% to ≤70 wt.-% of at least one non-ionic ethylenically unsaturated monomer selected from the group consisting of methyl, ethyl, butyl or 2-ethyl-hexyl esters of acrylic and methacrylic acid; acrylonitrile; vinyl acetate; styrene; methylstyrene; diisobutylene; vinylpyrrolidone and vinylcaprolactam, (C) ≥1 wt.-% to ≤40 wt.-% of at least one monomer of formula (I) ##STR00010## wherein R.sub.1 denotes hydrogen or methyl, n is a real number in the range of ≥10 to ≤80, and R.sub.1 denotes branched, unsubstituted C.sub.10-C.sub.15 alkyl, (D) ≥0 wt.-% to ≤1 wt.-% of at least one crosslinking reagent selected from the group consisting of ethylene glycol diacrylate; ethylene glycol dimethacrylate; trimethylolpropanetriacrylate; trimethylolpropanetrimethacrylate; allyl acrylate; methylenebisacrylamide; methylenebismethacrylamide; tetrallyloxyethane; triallylcyanurates; allylic ethers of pentaerythritol, sorbitol, or sucrose, and a diallylester of phthalic acid, (E) ≥0 wt.-% to ≤10 wt.-% of at least one ethylenically unsaturated monomer which is different from (A), (B), and (C), selected from the group consisting of linear, branched, cycloaliphatic or arylaliphatic esters of acrylic or methacrylic acids; isomers of butyl (meth)acrylate; isomers of hexyl (meth)acrylate, n-octyl (meth)acrylate, 2-ethylhexyl (meth)acrylate, 1-decyl (meth)acrylate, 2-decyl (meth)acrylate or isodecyl (meth)acrylate; isomers of dodecyl (meth)acrylate, cyclohexyl (meth)acrylate, isobornyl (meth)acrylate or benzyl (meth)acrylate; vinylaromatic monomers; and amide or nitrile derivatives of (meth)acrylic acids, (F) ≥0 wt.-% to ≤1 wt.-% of at least one chain transfer agent selected from the group consisting of N-dodecyl mercaptan; n-decyl mercaptan; octyl mercaptan; 1,8-dimercapto-3,6-dioxaoctane; thiolactic acid; tert-dodecanthiol; 2 (ethylhexyl)thioglycolate and terpinolene, wherein wt.-% is based on the total weight of the mixture, and wherein the C.sub.10-C.sub.15 alkyl has a mean degree of branching (iso-index) in the range of ≥1.5 to ≤3.5.
30. The copolymer according to claim 1, which is obtainable obtained by reacting a mixture comprising: (A) ≥30 wt.-% to ≤70 wt.-% of at least one ethylenically unsaturated monomer with a carboxylic function selected from the group consisting of acrylic acid; methacrylic acid; C.sub.1 to C.sub.4 monoesters of maleic or itaconic acids, and mixtures thereof; and ethylenically unsaturated monomer with a carboxylic function, consisting of crotonic, isocrotonic, cinnamic, itaconic, maleic acid, and maleic anhydride, (B) ≥30 wt.-% to ≤70 wt.-% of at least two different non-ionic ethylenically unsaturated monomers selected from the group consisting of methyl, ethyl, butyl or 2-ethyl-hexyl esters of acrylic and methacrylic acid, acrylonitrile; vinyl acetate; styrene; methylstyrene; diisobutylene; vinylpyrrolidone and vinylcaprolactam, (C) ≥1 wt.-% to ≤40 wt.-% of at least two different monomers of formula (I) ##STR00011## wherein R.sub.1 denotes hydrogen or methyl, n is a real number in the range of ≥10 to 80, and R.sub.2 denotes branched, unsubstituted C.sub.10-C.sub.15 alkyl, (D) ≥0 wt.-% to ≤1 wt.-% of at least one crosslinking reagent selected from the group consisting of ethylene glycol diacrylate; ethylene glycol dimethacrylate; trimethylolpropanetriacrylate; trimethylolpropanetrimethacrylate allyl acrylate; methylenebisacrylamide; methylenebismethacrylamide; tetrallyloxyethane; triallylcyanurates; allylic ethers of pentaerythritol, sorbitol, or sucrose, and a diallylester of phthalic acid, (E) ≥0 wt.-% to ≤10 wt.-% of at least one ethylenically unsaturated monomer which is different from (A), (B), and (C), selected from the group consisting of linear, branched, cycloaliphatic or arylaliphatic esters of acrylic or methacrylic acids; isomers of butyl (meth)acrylate; isomers of hexyl (meth)acrylate, n-octyl (meth)acrylate, 2-ethylhexyl (meth)acrylate, 1-decyl (meth)acrylate, 2-decyl (meth)acrylate or isodecyl (meth)acrylate, isomers of dodecyl (meth)acrylate, cyclohexyl (meth)acrylate, isobornyl (meth)acrylate or benzyl (meth)acrylate; vinylaromatic monomers and amide or nitrile derivatives of (meth)acrylic acids, (F) ≥0 wt.-% to ≤1 wt.-% of at least one chain transfer agent selected from the group consisting of N-dodecyl mercaptan; n-decyl mercaptan; octyl mercaptan; 1,8-dimercapto-3,6-dioxaoctane; thiolactic acid; tert-dodecanthiol; 2-(ethylhexyl)thioglycolate and terpinolene, wherein wt.-% is based on the total weight of the mixture, and wherein the C.sub.10-C.sub.15 alkyl has a mean degree of branching (iso-index) in the range of ≥1.5 to ≤3.5.
31. The copolymer according to claim 1, which is obtained by reacting a mixture comprising: (A) ≥36 wt.-% to ≤64 wt.-% of at least one ethylenically unsaturated monomer with a carboxylic function selected from the group consisting of acrylic acid; methacrylic acid; and C.sub.1 to C.sub.4 monoesters of maleic or itaconic acids, (B) ≥40 wt.-% to ≤60 wt.-% of at least two different non-ionic ethylenically unsaturated monomers selected from the group consisting of methyl, ethyl, butyl or 2-ethyl-hexyl esters of acrylic and methacrylic acid, (C) ≥8 wt.-% to ≤30 wt.-% of at least two different monomers of formula (I) ##STR00012## wherein R.sub.1 denotes methyl, n is a real number in the range of ≥10 to ≤60, and R.sub.2 denotes branched, unsubstituted C.sub.12-C.sub.15 alkyl, (D) ≥0 wt.-% to ≤0.5 wt.-% of at least one crosslinking reagent selected from the group consisting of ethylene glycol diacrylate; ethylene glycol dimethacrylate; trimethylolpropanetriacrylate; trimethylolpropanetrimethacrylate; allyl acrylate; methylenebisacrylamide; methylenebismethacrylamide; tetrallyloxyethane; triallylcyanurates; allylic ethers of pentaerythritol, sorbitol, or sucrose, and a diallylester of phthalic acid, (E) ≥0 wt.-% to ≤5 wt.-% of at least one ethylenically unsaturated monomer which is different from (A), (B), and (C), selected from the group consisting of linear, branched, cycloaliphatic or arylaliphatic esters of acrylic or methacrylic acids, isomers of butyl (meth)acrylate; isomers of hexyl (meth)acrylate, n-octyl (meth)acrylate, 2-ethylhexyl (meth)acrylate, 1-decyl (meth)acrylate, 2-decyl (meth)acrylate or isodecyl (meth)acrylate; isomers of dodecyl (meth)acrylate, cyclohexyl (meth)acrylate, isobornyl (meth)acrylate or benzyl (meth)acrylate; vinylaromatic monomers; and amide or nitrile derivatives of (meth)acrylic acids, (F) ≥0 wt.-% to ≤0.5 wt.-% of at least one chain transfer agent selected from the group consisting of N-dodecyl mercaptan; n-decyl mercaptan; octyl mercaptan; 1,8-dimercapto-3,6-dioxaoctane; thiolactic acid; tert-dodecanthiol; 2-(ethylhexyl)thioglycolate and terpinolene, wherein wt.-% is based on the total weight of the mixture, and wherein the C.sub.12-C.sub.15 alkyl has a mean degree of branching (iso-index) in the range of ≥1.8 to ≤2.8.
32. The copolymer according to claim 1 which is obtained by reacting a mixture consisting of: (A) ≥30 wt.-% to ≤70 wt.-% of at least one ethylenically unsaturated monomer with a carboxylic function, (B) ≥30 wt.-% to ≤70 wt.-% of at least one non-ionic ethylenically unsaturated monomer, (C) ≥1 wt.-% to ≤40 wt.-% of at least one monomer of formula (I) ##STR00013## wherein R.sub.1 denotes hydrogen or methyl, n is a real number in the range of ≥10 to 80, and R.sub.2 denotes branched, unsubstituted C.sub.10-C.sub.15 alkyl, (D) ≥0 wt.-% to ≤1 wt.-% of at least one crosslinking reagent, (E) ≥0 wt.-% to ≤10 wt.-% of at least one ethylenically unsaturated monomer which is different from (A), (B), and (C), and (F) ≥0 wt.-% to ≤1 wt.-% of at least one chain transfer agent, and wherein wt.-% is based on the total weight of the mixture, and wherein the C.sub.10-C.sub.15 alkyl has a mean degree of branching (iso-index) in the range of ≥1.5 to ≤3.5.
33. The copolymer according to claim 32, wherein the C.sub.10-C.sub.15 alkyl has a mean degree of branching (iso-index) in the range of ≥1.8 to ≤2.8.
34. The copolymer according to claim 1, wherein the at least one non-ionic ethylenically unsaturated monomer (B) is selected from the group consisting of 1) methyl, ethyl, butyl or 2-ethyl-hexyl esters of acrylic and methacrylic acid; 2) acrylonitrile; 3) vinyl acetate; 4) styrene; 5) methylstyrene; 6) diisobutylene, vinylpyrrolidone, and 7) vinylcaprolactam.
35. A method for manufacturing the copolymer according to claim 1, the method comprising: copolymerizing in a liquid medium a monomer mixture comprising: (A) ≥30 wt.-% to ≤70 wt.-% of at least one ethylenically unsaturated monomer with a carboxylic function, (B) ≥30 wt.-% to ≤70 wt.-% of at least one non-ionic ethylenically unsaturated monomer, (C) ≥1 wt.-% to ≤40 wt.-% of at least one monomer of formula (I), and ##STR00014## wherein R.sub.1 denotes hydrogen or methyl, n is a real number in the range of ≥10 to ≤80, and R.sub.2 denotes branched, unsubstituted C.sub.10-C.sub.15 alkyl, and (D) ≥0 wt.-% to ≤1 wt.-% of at least one crosslinking reagent, (E) ≥0 wt.-% to ≤10 wt.-% of at least one ethylenically unsaturated monomer which is different from (A), (B), and (C), and (F) ≥0 wt.-% to ≤1 wt.-% of at least one chain transfer agent, wherein wt.-% is based on the total weight of the mixture, and wherein the C.sub.10-C.sub.15 alkyl has a mean degree of branching (iso-index) in the range of ≥1.5 to ≤3.5.
36. The method according to claim 35, wherein the liquid medium comprises water, surfactants, said crosslinking agent, said chain transfer agent and an initiator.
37. An aqueous composition in the form of a coating formulation, which comprises: ≥0.01 wt.-% to ≤10 wt.-%, based on the total weight of the aqueous composition, of at least one copolymer according to claim 1, ≥15 wt.-% to ≤99.9 wt.-%, based on the total weight of the aqueous composition, of water and at least one component selected from the group consisting of pigments, fillers, binders, solvents, defoamers, a neutralising agent, a wetting agent, and pigment dispersing agents.
38. The aqueous composition according to claim 37, wherein the composition is a paint, lacquer, varnish, paper coating, wood coating, adhesive, cosmetic formulation, detergent formulation, textile and drilling muds plaster formulations, formulations for plasterboard, formulations for hydraulic binders, formulations for ceramics and formulations for leather.
Description
DETAILED DESCRIPTION OF THE INVENTION
(1) The presently claimed invention is directed to a HASE copolymer which acts as an effective thickener at high shear rates and creates a Newtonian rheology profile in aqueous coating formulations. The copolymer comprises at least one ethylenically unsaturated monomer with a carboxylic function (A), at least one non-ionic ethylenically unsaturated monomer (B), at least one monomer (C) of formula (I) which is an oxyalkylated monomer with ethylenic unsaturation and terminated by a hydrophobic branched unsubstituted C.sub.10-C.sub.15 alkyl chain having a mean degree of branching (iso-index) in the range of ≥1.5 to ≤3.5, optionally, at least one crosslinking reagent (D), optionally, at least one ethylenically unsaturated monomer (E) which is different from (A), (B), (C) and (D), and optionally at least one chain transfer agent (F).
(2) Accordingly, the presently claimed invention is directed to a copolymer which is obtainable by reacting a mixture comprising: (A) ≥30 wt.-% to ≤70 wt.-% of at least one ethylenically unsaturated monomer with a carboxylic function, (B) ≥30 wt.-% to ≤70 wt.-% of at least one non-ionic ethylenically unsaturated monomer, (C) ≥1 wt.-% to ≤40 wt.-% of at least one monomer of formula (I)
(3) ##STR00007## wherein R.sub.1 denotes hydrogen or methyl, n is a real number in the range of ≥10 to ≤80, and R.sub.2 denotes branched, unsubstituted C.sub.10-C.sub.15 alkyl, (D) ≥0 wt.-% to ≤1 wt.-% of at least one crosslinking reagent, (E) ≥0 wt.-% to ≤10 wt.-% of at least one ethylenically unsaturated monomer which is different from (A), (B), and (C), (F) ≥0 wt.-% to ≤1 wt.-% of at least one chain transfer agent, and
wherein wt.-% is based on the total weight of the mixture,
characterized in that the C.sub.10-C.sub.15 alkyl has a mean degree of branching (iso-index) in the range of ≥1.5 to ≤3.5.
(4) The term “thickener” as used herein shall be understood to mean a compound which when added, increases the viscosity of the composition, in particular the viscosity at a high shear rate (1000 s.sup.−1 to 10000 s.sup.−1).
(5) When the copolymer of the presently claimed invention having a monomer (C) of formula (I) with C.sub.10-C.sub.15 alkyl having a mean degree of branching (iso-index) in the range from 1.5-3.5 is used as a thickener, it imparts the desired thickening effect. By “desired thickening effect” it is meant that it exhibits high thickening efficiency at high shear rates, i.e. at shear rate of 1000 s.sup.−1 to 10000 s.sup.−1, but at the same time does not lead to unwanted thickening effect at low shear rates of 0.1 to 100 s.sup.−1 thereby creating a Newtonian rheology profile. For aqueous compositions in form of coating formulations, ≥0.01 wt.-% to ≤10 wt.-% based on total weight of the aqueous composition, of the copolymer of the presently claimed invention is added to obtain the desired thickening effect.
(6) The term “branched” denotes a chain of atoms with one or more side chains attached to it. Branching occurs by the replacement of a substituent, e.g. a hydrogen atom, with a covalently bonded alkyl radical.
(7) The term “alkyl” denotes a saturated moiety constituted solely of atoms of carbon and of hydrogen.
(8) Preferably in the copolymer according to the presently claimed invention, as described hereinabove, at least one ethylenically unsaturated monomer with a carboxylic function (A) is present, preferably in an amount ≥30 wt.-% to ≤70 wt.-% or in an amount ≥33 wt.-% to ≤67 wt.-%, more preferably in an amount of ≥36 wt.-% to ≤64 wt.-% or in an amount of ≥36 wt.-% to ≤55 wt.-% or in an amount of ≥38 wt.-% to ≤55 wt.-%, most preferably in an amount of ≥38 wt.-% to ≤50 wt.-%, or in an amount of ≥38 wt.-% to ≤45 wt.-%, based on total weight of the mixture.
(9) Preferably, the copolymer according to the presently claimed invention has an average molecular weight of ≥10000 g/mol to ≤3000000 g/mol.
(10) In an embodiment of the presently claimed invention, the at least one non-ionic ethylenically unsaturated monomer (B) is a mixture of at least two different non-ionic ethylenically unsaturated monomers (B). For example, monomer (B) is a mixture of ethyl, butyl or 2-ethyl-hexyl esters of acrylic and methacrylic acid, acrylonitrile, vinyl acetate, styrene, methylstyrene, diisobutylene, vinylpyrrolidone and vinylcaprolactam.
(11) In an embodiment of the presently claimed invention, the at least one monomer (C) is a mixture of at least two different monomers of formula (I). For example, monomer (C) is a mixture of different monomers comprising C.sub.10 to C.sub.15 alkyl having a mean degree of branching (iso-index) in the range of ≥1.5 to ≤3.5.
(12) In an embodiment of the presently claimed invention, the hydrophobic branched chain is derived from C.sub.10-C.sub.15 alcohols having a mean degree of branching (iso-index) in the range of ≥1.5 to ≤3.5.
(13) In another embodiment of the presently claimed invention, the hydrophobic branched chain is derived from C.sub.12-C.sub.13 alcohols having a mean degree of branching (iso-index) in the range of ≥1.5 to ≤3.5.
(14) Such branched alcohols from commercial sources are typically not molecular uniform compounds, but consist of a complex mixtures of isomers, depending on the technical manufacturing process. They can therefore not be described by a single chemical formula, but can best be described by the C-length distribution and the Iso-Index “Ix”.
(15) The mean degree of branching (iso-index) of the monomer (C) of formula (I) is essential to the invention since a mean degree of branching (iso-index) in the range from 1.5-3.5 imparts the desired thickening effect to the coating formulation. In the context of the present invention, the mean degree of branching is generally defined as the number of methyl groups in a molecule of the alcohol minus 1. The mean degree of branching is the statistical mean of the degrees of branching of the molecules of a sample.
(16) The mean degree of branching can be determined by .sup.1H-NMR spectroscopy as follows: A sample of the alcohol or alcohol mixture, for instance the C.sub.12 alcohol or the C.sub.12/C.sub.13 alcohol mixture, is first subjected to a derivatization with trichloroacetyl isocyanate (TAI). This converts the alcohols to the carbamic esters.
(17) The signals of the primary alcohols esterified in this way are at δ=4.7 to 4.0 ppm, those of esterified secondary alcohols (where present) at about 5 ppm, and water present in the sample reacts with TAI to give the carbamic acid. All methyl, methylene and methine protons are in the range from 2.4 to 0.4 ppm. The signals <1 ppm are assigned to the methyl groups. From the spectrum thus obtained, it is possible to calculate the mean degree of branching (iso index) as follows:
iso index=((F(CH.sub.3)/3)/(F(CH.sub.2OH)/2))−1
where F(CH.sub.3) is the signal area corresponding to the methyl protons and F(CH.sub.2OH) is the signal area of the methylene protons in the CH.sub.2OH group.
(18) U.S. Pat. No. 7,335,235 provides a process for the preparation of the alkoxylate mixtures by reacting alkanols with alkylene oxides, under alkoxylation conditions, in the presence of a catalyst. Preferably the alcohol, more preferably the C.sub.10-C.sub.15 alcohols having a mean degree of branching (iso-index) in the range of ≥1.5 to ≤3.5, and KOH (finely powdered) are mixed and dewatered at 80° C. and 40 mbar for 1 hour. The reaction product is placed into an autoclave, the autoclave is preferably rendered inert by flushing twice with nitrogen and is then heated to 120° C. Over the course of 15 minutes, ethylene oxide is metered in to a maximum pressure of 1 bar. This pressure is held for 5 min, then increased by adding ethylene oxide over the course of 60 minutes to 3 bar, this pressure is held for 5 hours and, finally, the pressure is increased to 6 bar. In the case of the last metered addition, only enough ethylene oxide is added until the amount of ethylene oxide given below is reached. The pressure is then held at 6 bar through the metered addition of nitrogen. After a reaction time of a further 10 hours, the system is left to cool to room temperature and the reaction product is removed. Volatile components are removed on a rotary evaporator at 30 mbar and 80° C.
(19) In a preferred embodiment, the alcohol alkoxylates to be used are based on C.sub.13-oxo alcohols. The term “C.sub.13-oxo alcohol” refers to an alcohol mixture whose main component is formed by at least one branched C.sub.13-alcohol (iso-tridecanol). Such C.sub.13-alcohols include, in particular, tetramethylnonanols, for example 2,4,6,8-tetramethyl-1-nonanol or 3,4,6,8-tetramethyl-1-nonanol and furthermore ethyldimethylnonanols such as 5-ethyl-4,7-dimethyl-1-nonanol.
(20) The general procedure to obtain C.sub.13-alcohol mixtures has been provided in U.S. Pat. No. 8,877,681. It is mentioned in U.S. Pat. No. 8,877,681 that suitable C.sub.13-alcohol mixtures can generally be obtained by hydrogenation of hydroformylated trimeric butene. In particular, it is possible to proceed as follows:
(21) a) butenes are brought into contact with a suitable catalyst for oligomerization,
(22) b) a C.sub.12-olefin fraction is isolated from the reaction mixture,
(23) c) the C.sub.12-olefin fraction is hydroformylated by reaction with carbon monoxide and hydrogen in the presence of a suitable catalyst, and
(24) d) hydrogenated.
(25) The butene trimerization (process step a) can be carried out with homogeneous or heterogeneous catalyst. Butenes are oligomerized in a homogeneous phase in the presence of a catalyst system comprising a transition metal derivative and an organometallic compound. Typical catalyst systems are Ni(O) complexes in combination with Lewis acids such as AlCl.sub.3, BF.sub.3, SbF.sub.5 and the like, or Ni(II) complexes in combination with alkylaluminum halides. However, it is also possible to oligomerize butenes in the manner known per se using a heterogeneous nickel-containing catalyst (process step a). Depending on the selected reaction conditions, different relative amounts of butene dimers, trimers and higher oligomers are obtained. The butene trimers, i.e. C.sub.12-olefins, are further processed for the present purposes. The isobutene content may be selected with a view to the desired degree of branching of the C.sub.13-alcohol mixture obtained after the hydroformylation/hydrogenation. Relatively low degrees of branching require a relatively low isobutene content and vice versa. If, for example, the C.sub.12-olefin fraction is to have an Iso-index of approximately 1.9 to 2.3, it is expedient to select predominantly linear butenes, i.e. the hydrocarbon stream which is generally employed should contain less than 5% by weight of isobutene based on the butene fraction. The butenes may contain an admixture of saturated C.sub.4-hydrocarbons, which act as diluent in the oligomerization process. The heterogeneous nickel-containing catalysts which may be used can have different structures, with catalysts containing nickel oxide being preferred. Catalysts which are known are described in C. T. O'Connor et al., Catalysis Today, vol. 6 (1990), pp. 336-338 are suitable.
(26) Starting with the material obtained in the oligomerization reaction, a C.sub.12-olefin fraction is isolated in one or more separation steps (process step b).
(27) The Iso-index of the C.sub.12-olefin fraction, which indicates the mean degree of branching, is generally from 1.5 to 3.5, preferably 1.8 to 2.8, more preferably 2 to 2.5. The iso index can be determined by the general procedure as discussed above.
(28) To prepare an alcohol mixture according to the invention, the C.sub.12-olefin fraction which has been isolated is hydroformylated to give C.sub.13-aldehydes (process step c), and these are subsequently hydrogenated to form C.sub.13-alcohols (process step d). The preparation of the alcohol mixture can be carried out in a single step or in two separate reaction steps.
(29) An overview of hydroformylation processes and suitable catalysts can be found in Beller et al., Journal of Molecular Catalysis A 104 (1995), pp. 17-85.
(30) The hydroformylation is preferably carried out in the presence of a cobalt hydroformylation catalyst.
(31) The crude aldehydes or aldehyde/alcohol mixtures obtained in the hydroformylation can, if desired, be isolated before hydrogenation by customary methods known to the skilled worker and, if appropriate, purified.
(32) For the hydrogenation, the reaction mixtures obtained in the hydroformylation are reacted with hydrogen in the presence of hydrogenation catalysts. Suitable hydrogenation catalysts are generally transition metals such as, for example, Cr, Mo, W, Fe, Rh, Co, Ni, Pd, Pt, Ru and the like or mixtures of these, which may be applied to supports such as active charcoal, aluminum oxide, kieselguhr and the like, to increase activity and stability.
(33) In theory, a “Newtonian” rheology profile signifies that the viscosity remains independent of the shearing gradient, however, such properties are believed impossible in polymer reality. Thus, in conventional practice, the skilled man in the art associates such a “Newtonian” profile with a low degree of change of viscosity depending on the shearing rate (rheogram proportionately flatter), in contrast to a pseudo-plastic rheology profile, characterised by a marked fall in the viscosity depending on this gradient (rheogram proportionately more sloping). In tangible terms, the lower the ratio between the low shear viscosity at 1 s.sup.−1, in mPas, and the high shear viscosity known as the “ICI” (which corresponds approximately to a shear rate of 10000 s.sup.−1), the closer one comes to a Newtonian behaviour.
(34) The copolymer of the presently claimed invention is obtained by the copolymerisation techniques well known to the skilled man in the art, such as the techniques of radical copolymerisation in solution, in a direct or reverse emulsion polymerization, in suspension, or precipitation in appropriate solvents, in the presence of catalytic systems and known chain transfer agents.
(35) In an embodiment of the presently claimed invention, a method for manufacturing the copolymer according to the present invention has been provided, the method comprises coploymerizing in a liquid medium a monomer mixture comprising: (A) ≥30 wt.-% to ≤70 wt.-% at least one ethylenically unsaturated monomer with a carboxylic function, (B) ≥30 wt.-% to ≤70 wt.-% at least one non-ionic ethylenically unsaturated monomer, (C) ≥1 wt.-% to ≤40 wt.-% at least one monomer of formula (I), and
(36) ##STR00008## wherein R.sub.1 denotes hydrogen or methyl, n is a real number in the range of ≥10 to ≤80, and R.sub.2 denotes branched, unsubstituted C.sub.10-C.sub.15alkyl, and (E) ≥0 wt.-% to ≤5 wt.-% at least one ethylenically unsaturated monomer which is different from (A), (B), and (C).
(37) In an embodiment according the presently claimed invention the liquid medium comprises water, surfactants, crosslinking reagent, chain transfer agent and an initiator.
Surfactant
(38) Surfactants which are preferably used for preparing the copolymer according to the present invention are selected from ionic surfactants and non-ionic surfactants, more specifically, anionic surfactants, for example, alcohol sulfates, alcohol ether sulfates, alkylbenzenesulfonates, α-olefinsulfonates, sulfosuccinates, and cationic surfactants, for example, C.sub.8 to C.sub.16-dialkyldimethylammonium salts, dialkoxydimethylammonium salts or imidazolinium salts with a long-chain alkyl radical. Non-ionic surfactants used are generally known in the art, preferably for example, ethoxylated fatty alcohols, ethoxylated alkylphenols and alkylpolyglycosides. For example, WO2013064761 provides polyglycerol as surfactant in the polymerization process for preparing acrylic associative thickener.
Crosslinking Reagent
(39) Crosslinking reagent is preferably selected from the group consisting of ethylene glycol diacrylate, ethylene glycol dimethacrylate, trimethylolpropanetriacrylate, trimethylolpropanetrimethacrylate, allyl acrylate, methylenebisacrylamide, methylenebismethacrylamide, tetrallyloxyethane, triallylcyanurates, and allylic ethers of pentaerythritol, sorbitol, or sucrose or diallylester of phthalic acid.
Chain Transfer Agent
(40) Chain transfer agent is preferably selected from the group consisting of N-dodecyl mercaptan, n-decyl mercaptan, octyl mercaptan, 1,8-dimercapto-3,6-dioxaoctane, thiolactic acid and tert-dodecanthiol, 2-(ethylhexyl)thioglycolate and terpinolene.
Initiator
(41) The radical emulsion polymerization is preferably initiated by a radical initiator, i.e. a compound, which, on exposure to heat or light, decomposes and forms free radicals, which triggers a radical polymerization of the ethylenically unsaturated monomers The initiators that are suitable for the emulsion polymerization of the invention are the polymerization initiators which are suitable and used typically for an emulsion polymerization, and which trigger free-radical polymerization of the monomers These initiators include azo compounds such as 2,2′-azobisisobutyronitrile, 2,2′-azobis(2-methyl-butyro-nitrile), 2,2′-azobis(2,4-dimethylvaleronitrile), 2,2′-azobis(4-methoxy-2,4-dimethylvalero-nitrile), 1,1′-azobis(1-cyclohexanecarbonitrile), 2,2′-azobis(isobutyramide) dihydrate, 2-phenylazo-2,4-dimethyl-4-methoxyvaleronitrile, dimethyl-2,2′-azobisisobutyrate, 2-(carbamoylazo)isobutyronitrile, 2,2′-azobis(2,4,4-trimethylpentane), 2,2′-azobis(2-methylpropane), 2,2′-azobis(N,N′-dimethyleneisobutyramidine), free base or hydrochloride, 2,2′-azobis(2-amidinopropane), free base or hydrochloride, 2,2′-azobis{2-methyl-N-[1,1-bis(hydroxy-methyl)ethyl]propionamide} or 2,2′-azobis{2-methyl-N[1,1-bis(hydroxymethyl)-2-hydroxy-ethyl]propionamide; organic peroxides or hydroperoxides such as acetyl cyclohexane sulphonyl peroxide, diisopropyl peroxy dicarbonate, t-amyl perneodecanoate, t-butyl perneodecanoate, t-butyl perpivalate, t-amylperpivalate, bis(2,4-dichlorobenzoyl)peroxide, diisononanoyl peroxide, didecanoyl peroxide, dioctanoyl peroxide, dilauroyl peroxide, bis (2-methylbenzoyl) peroxide, disuccinic acid peroxide, di-acetyl peroxide, dibenzoyl peroxide, t-butyl per 2-ethylhexanoate, bis-(4-chlorobenzoyl)-peroxide, t-butyl perisobutyrate, t-butyl permaleinate, 1,1-bis(t-butylperoxy)3,5,5-trimethyl-cyclohexane, 1,1-bis(t-butylperoxy)cyclohexane, t-butyl peroxy isopropyl carbonate, t-butyl perisononaoate, 2,5-dimethylhexane 2,5-dibenzoate, t-butyl peracetate, t-amyl perbenzoate, t-butyl perbenzoate, 2,2-bis (t-butylperoxy) butane, 2,2 bis (t-butylperoxy) propane, dicumyl peroxide, 2,5-dimethylhexane-2,5-di-t-butylperoxide, 3-t-butylperoxy 3-phenylphthalide, di-t-amyl peroxide, [alpha], [alpha]′-bis(t-butylperoxy isopropyl) benzene, 3,5-bis (t-butylperoxy)3,5-dimethyl 1,2-dioxolane, di-t-butyl peroxide, 2,5-dimethylhexyne-2,5-di-t-butylperoxide, 3,3,6,6,9,9-hexamethyl 1,2,4,5-tetraoxa cyclononane, p-menthane hydroperoxide, pinane hydroperoxide, diisopropylbenzene mono-[alpha]-hydroperoxide, cumene hydroperoxide, t-butyl hydroperoxide and diisopropyl peroxidicarbamate, inorganic peroxides and hydroperoxides such as H.sub.2O.sub.2 and salts of peroxodisulfuric acid such as sodium peroxodisulfate, and redox initiator systems, which comprise an oxidizing agent, e.g. one or more of the aforementioned organic or inorganic peroxides or hydroperoxides and a reducing agent, e.g. a sulfur compound which more particularly is selected from sodium hydrogen sulfite, sodium hydroxymethanesulfinate, and the adduct of hydrogen sulfite with acetone, or ascorbic acid. Redox initiator systems may further comprise an addition of small amounts of redox metal salts such as iron salts, vanadium salts, copper salts, chromium salts or manganese salts, such as in the ascorbic acid/iron (II) sulfate sodium peroxodisulfate redox initiator system, for example.
(42) It is preferred to use water-soluble initiators, examples being salts of peroxodisulfuric acid, more particularly sodium, potassium or ammonium salts, or a redox initiator system comprising as oxidizing agent a salt of peroxodisulfuric acid, hydrogen peroxide or an organic peroxide such as tert-butyl hydroperoxide. The reducing agents preferably comprise a sulfur compound which more particularly is selected from sodium hydrogen sulfite, sodium hydroxymethanesulfinate, and the adduct of hydrogen sulfite with acetone. Other suitable reducing agents are phosphorus-containing compounds such as phosphorous acid, hypophosphites, and phosphinates and also hydrazine or hydrazine hydrate, and ascorbic acid.
(43) The initiator is used typically in an amount of ≥0.02% to ≤2%, and more particularly ≥0.05% to ≤1.5%, by weight, based on the overall amount of monomers at least one ethylenically unsaturated monomer with a carboxylic function (A), at least one non-ionic ethylenically unsaturated monomer (B), at least one monomer (C) of formula (I) and at least one ethylenically unsaturated monomer (E) which is different from (A), (B), and (C). The optimum amount of initiator is of course dependent on the initiator system used and can be determined by the skilled worker in routine experiments. Particularly, monomer (A) is selected from the group consisting of acrylic acid, methacrylic acid, C.sub.1 to C.sub.4 monoesters of maleic or itaconic acids, and mixtures thereof, or is selected from the group consisting of ethylenically unsaturated monomer with a carboxylic function, consisting of crotonic, isocrotonic, cinnamic, itaconic, maleic acid, and maleic anhydride.
(44) In an embodiment of the presently claimed invention aqueous composition in the form of a coating formulation, which comprises ≥0.01 wt.-% to ≤10 wt.-%, preferably, ≥0.1 wt.-% to ≤10 wt.-%, preferably, ≥0.3 wt.-% to ≤10 wt.-%, more preferably, ≥0.7 wt.-% to ≤10 wt.-%, based on the total weight of the aqueous composition, the copolymer according to the present invention, and ≥15 wt.-% to ≤99.9≤wt.-%, preferably, ≥30 wt.-% to ≤99.9≤wt.-%, more preferably, ≥50 wt.-% to 99≤wt.-%, based on the total weight of the aqueous composition of at least one of the components, selected from the group consisting of pigments, fillers, binders, solvents, defoamers, neutralising agent, wetting agent, pigment dispersing agents and water.
Additives
(45) The choice of suitable conventional additives for the composition of the invention is dependent on the particular end use of the coating material formulations, and may be determined in an individual case by the skilled person. The following compounds are generally used as additives.
Pigments
(46) Organic or inorganic pigments are suitable as additives. Examples of organic pigments are color pigments and mother-of-pearl-like pigments such as azo, disazo, naphthol, benzimidazolone, azo condensation, metal complex, isoindolinone, quinophthalone, and dioxazine pigments, polycyclic pigments such as indigo, thioindigo, quinacridones, phthalocyanines, perylenes, perinones, anthraquinones, e.g., aminoanthraquinones or hydroxyanthraquinones, anthrapyrimidines, indanthrones, flavanthrones, pyranthrones, anthanthrones, isoviolanthrones, diketopyrrolopyrroles, and also carbazoles, e.g., carbazole violet, and the like. Other examples of organic pigments can be found in the following monograph: W. Herbst, K. Hunger, “Industrielle Organische Pigmente”, 2.sup.nd edition, 1995, VCH Verlagsgesellschaft, ISBN: 3-527-28744-2. Examples of inorganic pigments are titanium dioxide, metallic flakes, such as aluminum and also aluminum oxide, iron (III) oxide, chromium (III) oxide, titanium (IV) oxide, zirconium (IV) oxide, zinc oxide, zinc sulfide, zinc phosphate, mixed metal oxide phosphates, molybdenum sulfide, cadmium sulfide, graphite, vanadates such as bismuth vanadate, chromates, such as lead (IV) chromates, molybdates such as lead (IV) molybdate, and mixtures thereof.
Fillers
(47) Suitable fillers are, for example, organic or inorganic particulate materials such as, for example, calcium carbonates and silicates, and also inorganic fiber materials such as glass fibers, for example. Organic fillers as well, such as carbon fibers, and mixtures of organic and inorganic fillers, such as mixtures of glass fibers and carbon fibers or mixtures of carbon fibers and inorganic fillers, for example, may find application. The fillers can be added in an amount of 1 to 75 wt. %, based on the total weight of the composition.
Binders
(48) Suitable binders are the ones customarily used, for example the ones described in 30 Ullmann's Encyclopedia of Industrial Chemistry, 5th Edition, Vol. A18, pp. 368-426, VCH, Weinheim 1991, Germany. In general, the film-forming binder is based on a thermoplastic or thermosetting resin, predominantly on a thermosetting resin. Examples thereof are alkyd, acrylic, polyester, phenolic, melamine, epoxy and polyurethane resins and mixtures thereof. Also resins curable by radiation or air-drying 35 resins can be used. Binders may also be derived from polyvinylalcohol and polyvinylbutyral. Binders include latex polymers made by emulsion polymerization. For architectural coatings especially preferred latex polymers are based on acrylic emulsion polymers, styrene-acrylic emulsion polymers, vinyl acetate-acrylic emulsion polymers or emulsion polymers based on ethylene and vinyl acetate. Preferably, the binder is present in the range of from 2 to 40 weight percent, more preferably in the range of from 5 to 30 weight percent, based on the weight of the paint composition.
Neutralizing Agent
(49) Suitable neutralizing agents are inorganic bases, organic bases, and combinations thereof. Examples of inorganic bases include but are not limited to the alkali metal hydroxides (especially lithium, sodium, potassium, magnesium, and ammonium), and alkali metal salts of inorganic acids, such as sodium borate (borax), sodium phosphate, sodium pyrophosphate, and the like; and mixtures thereof. Examples of organic bases include but are not limited to triethanolamine (TEA), diisopropanolamine, triisopropanolamine, aminomethyl propanol (2-Amino-2-methyl-1-propanol), dodecylamine, cocamine, oleamine, morpholine, triamylamine, triethylamine, tetrakis(hydroxypropyl)ethylenediamine, L-arginine, methyl glucamine, isopropylamine, aminomethyl propanol, tromethamine (2-amino 2-hydroxymethyl-1,3-propanediol), and PEG-15 cocamine. Alternatively, other alkaline materials can be used alone or in combination with the above mentioned inorganic and organic bases.
Other Rheology Modifiers
(50) As is common in many application fields to combine different rheology modifiers, the inventive aqueous compositions like paints may contain non-inventive rheology additives in addition to the inventive HASE copolymer according to the presently claimed invention.
(51) Depending on the intended use, the pigment composition may further comprise one or more conventional additives. Conventional additives included e.g. defoamers, wetting agents, pigment dispersing agents, pigment synergists, preservatives, and the like.
(52) Preferred embodiments a to p of the copolymer of the presently claimed invention are summarized in the Table 1 to 4.
(53) TABLE-US-00001 TABLE 1 Component(s) a b c d (A) at least one (A) is selected from the group (A) is selected from the group (A) is selected from (A) is selected from ethylenically consisting of acrylic acid, consisting of acrylic acid, the group consisting the group consisting unsaturated methacrylic acid, C.sub.1 to C.sub.4 methacrylic acid, C.sub.1 to C.sub.4 of acrylic acid, of acrylic acid, monomer with monoesters of maleic or itaconic monoesters of maleic or itaconic methacrylic acid, methacrylic acid, a carboxylic acids, and mixtures thereof, or is acids, and mixtures thereof, or is C.sub.1 to C.sub.4 monoesters C.sub.1 to C.sub.4 monoesters function selected from the group consisting selected from the group consisting of maleic or itaconic of maleic or itaconic of ethylenically unsaturated of ethylenically unsaturated acids, and mixtures acids, and mixtures monomer with a carboxylic monomer with a carboxylic thereof thereof function, consisting of crotonic, function, consisting of crotonic, isocrotonic, cinnamic, itaconic, isocrotonic, cinnamic, itaconic, maleic acid, and maleic anhydride maleic acid, and maleic anhydride (B) at least one (B) is selected from the group (B) is selected from the group (B) is selected from (B) is selected from non-ionic consisting of methyl, ethyl, butyl consisting of methyl, ethyl, butyl the group consisting the group consisting ethylenically or 2-ethyl-hexyl esters of acrylic or 2-ethyl-hexyl esters of acrylic of methyl, ethyl, of methyl, ethyl, unsaturated and methacrylic acid, acrylonitrile, and methacrylic acid, acrylonitrile, butyl or 2-ethyl- butyl or 2-ethyl- monomer vinyl acetate, styrene, vinyl acetate, styrene, hexyl esters of hexyl esters of methylstyrene, diisobutylene, methylstyrene, diisobutylene, acrylic, and acrylic, and vinylpyrrolidone, vinylcaprolactam vinylpyrrolidone, vinylcaprolactam methacrylic acid methacrylic acid (C) at least one Formula (I), wherein R.sub.1 denotes Formula (I), wherein R.sub.1 denotes Formula (I), wherein Formula (I), wherein monomer of hydrogen or methyl, n is a real hydrogen or methyl, n is a real R.sub.1 is methyl, R.sub.1 is methyl, formula (I) number in the range of ≥10 number in the range of ≥10 n is a real number n is a real number to ≤80, R.sub.2 denotes branched, to ≤70, R.sub.2 denotes branched, in the range of ≥10 in the range of≥10 unsubstituted C.sub.10-C.sub.15 alkyl, and unsubstituted C.sub.10-C.sub.15 alkyl, and to ≤60, R.sub.2 denotes to ≤50, R.sub.2 denotes C.sub.10-C.sub.15 alkyl has an iso-index in C.sub.10-C.sub.15 alkyl has an iso-index in branched, branched, the range of ≥1.5 to ≤3.5 the range of ≥1.5 to ≤3.5 unsubstituted C.sub.10-C.sub.15 unsubstituted C.sub.10-C.sub.15 alkyl, and C.sub.10-C.sub.15 alkyl, and C.sub.10-C.sub.15 alkyl has an iso-index alkyl has an iso-index in the range of ≥1.8 in the range of ≥2 to ≤2.8 to ≤2.5 Optionally, (D) (D) is selected from the group (D) is selected from the group (D) is selected from (D) is selected from at least one consisting of ethylene glycol consisting of ethylene glycol the group consisting the group consisting cross linking diacrylate, ethylene glycol diacrylate, ethylene glycol of ethylene glycol of ethylene glycol reagent dimethacrylate, trimethylolpropane- dimethacrylate, trimethylolpropane- diacrylate, ethylene diacrylate, ethylene triacrylate, trimethylolpropanetri- triacrylate, trimethylolpropanetri- glycol dimethacrylate, glycol dimethacrylate, methacrylate, allyl acrylate, meth- methacrylate, allyl acrylate, meth- trimethylolpropane- trimethylolpropane- ylenebisacrylamide, meth- ylenebisacrylamide, meth- triacrylate, tri- triacrylate, tri- ylenebismethacrylamide, tetral- ylenebismethacrylamide, tetral- methylolpropanetri- methylolpropanetri- lyloxyethane, triallylcyanurates, lyloxyethane, triallylcyanurates, methacrylate, allyl methacrylate, allyl and allylic ethers of and allylic ethers of acrylate, meth- acrylate, meth- pentaerythritol, sorbitol, or pentaerythritol, sorbitol, or ylenebisacrylamide, ylenebisacrylamide, sucrose or diallylester of phthalic sucrose or diallylester of phthalic methylenebismeth- methylenebismeth- acid acid acrylamide, tetral- acrylamide, tetral- lyloxyethane, tri- lyloxyethane, tri- allylcyanurates, allylcyanurates, and allylic ethers of and allylic ethers of pentaerythritol, pentaerythritol, sorbitol, or sucrose sorbitol, or sucrose or diallylester of or diallylester of phthalic acid phthalic acid Optionally, (E) (E) is selected from the group (E) is selected from the group (E) is selected from (E) is selected from at least one consisting of linear, branched, consisting of linear, branched, the group consisting the group consisting ethylenically cycloaliphatic or arylaliphatic cycloaliphatic or arylaliphatic of linear, branched, of linear, branched, unsaturated esters of acrylic or methacrylic esters of acrylic or methacrylic cycloaliphatic or cycloaliphatic or monomer acids, isomers of butyl acids, isomers of butyl arylaliphatic esters arylaliphatic esters which is (meth)acrylate, isomers of hexyl (meth)acrylate, isomers of hexyl of acrylic or of acrylic or different (meth)acrylate, n-octyl (meth)acrylate, n-octyl methacrylic acids, methacrylic acids, from (A), (meth)acrylate, 2-ethylhexyl (meth)acrylate, 2-ethylhexyl isomers of butyl isomers of butyl (B), and (C) (meth)acrylate, 1-decyl (meth)acrylate, 1-decyl (meth)acrylate, (meth)acrylate, (meth)acrylate, 2-decyl (meth)acrylate, 2-decyl isomers of hexyl isomers of hexyl (meth)acrylate, isodecyl (meth)acrylate, isodecyl (meth)acrylate, (meth)acrylate, (meth)acrylate, isomers of (meth)acrylate, isomers of n-octyl (meth)acrylate, n-octyl (meth)acrylate, dodecyl (meth)acrylate, dodecyl (meth)acrylate, 2-ethylhexyl 2-ethylhexyl cyclohexyl (meth)acrylate, cyclohexyl (meth)acrylate, (meth)acrylate, 1-decyl (meth)acrylate, 1-decyl isobornyl (meth)acrylate, benzyl isobornyl (meth)acrylate, benzyl (meth)acrylate, 2-decyl (meth)acrylate, 2-decyl (meth)acrylate, vinylaromatic (meth)acrylate, vinylaromatic (meth)acrylate, isodecyl (meth)acrylate, isodecyl monomers, amide or nitrile monomers, amide or nitrile (meth)acrylate, isomers (meth)acrylate, isomers derivatives of (meth)acrylic acids derivatives of (meth)acrylic acids of dodecyl (meth)acrylate, of dodecyl (meth)acrylate, cyclohexyl (meth)acrylate, cyclohexyl (meth)acrylate, isobornyl (meth)acrylate, isobornyl (meth)acrylate, benzyl (meth)acrylate, benzyl (meth)acrylate, vinylaromatic monomers, vinylaromatic monomers, amide or nitrile amide or nitrile derivatives of derivatives of (meth)acrylic acids (meth)acrylic acids (F) optionally, (F) is selected from the group (F) is selected from the group (F) is selected from (F) is selected from at least one consisting of n-dodecyl consisting of n-dodecyl the group consisting the group consisting chain transfer mercaptan, n-decyl mercaptan, mercaptan, n-decyl mercaptan, of n-dodecyl mercaptan, of n-dodecyl mercaptan, agent octyl mercaptan, 1,8- dimercapto- octyl mercaptan, 1,8- dimercapto- n-decyl mercaptan, n-decyl mercaptan, 3, 6-dioxaoctane, thiolactic acid 3, 6-dioxaoctane, thiolactic acid octyl mercaptan, octyl mercaptan, and tert-dodecanthiol, 2- and tert-dodecanthiol, 2- 1,8- dimercapto- 1,8- dimercapto- (ethylhexyl)thioglycolate and (ethylhexyl)thioglycolate and 3, 6-dioxaoctane, and 2- 3, 6-dioxaoctane and 2- terpinolene terpinolene (ethylhexyl)thioglycolate (ethylhexyl)thioglycolate
(54) TABLE-US-00002 TABLE 2 Component(s) e f g h (A) at least one (A) is selected from the group (A) is selected from the group (A) is selected from (A) is selected from ethylenically consisting of acrylic acid, consisting of acrylic acid, the group consisting the group consisting unsaturated methacrylic acid, C.sub.1 to C.sub.4 methacrylic acid, C.sub.1 to C.sub.4 of acrylic acid, of acrylic acid, monomer with monoesters of maleic or itaconic monoesters of maleic or itaconic methacrylic acid, methacrylic acid, a carboxylic acids, and mixtures thereof, or is acids, and mixtures thereof, or is C.sub.1 to C.sub.4 monoesters C.sub.1 to C.sub.4 monoesters function selected from the group consisting selected from the group consisting of maleic or itaconic of maleic or itaconic of ethylenically unsaturated of ethylenically unsaturated acids, and mixtures acids, and mixtures monomer with a carboxylic monomer with a carboxylic thereof thereof function, consisting of crotonic, function, consisting of crotonic, isocrotonic, cinnamic, itaconic, isocrotonic, cinnamic, itaconic, maleic acid, and maleic anhydride maleic acid, and maleic anhydride (B) at least two (B) is selected from the group (B) is selected from the group (B) is selected from (B) is selected from different consisting of methyl, ethyl, butyl consisting of methyl, ethyl, butyl the group consisting the group consisting nonionic or 2-ethyl-hexyl esters of acrylic or 2-ethyl-hexyl esters of acrylic of methyl, ethyl, of methyl, ethyl, ethylenically and methacrylic acid, acrylonitrile, and methacrylic acid, acrylonitrile, butyl or 2-ethyl- butyl or 2-ethyl- unsaturated vinyl acetate, styrene, vinyl acetate, styrene, hexyl esters of hexyl esters of monomer methylstyrene, diisobutylene, methylstyrene, diisobutylene, acrylic, and acrylic, and vinylpyrrolidone, vinylcaprolactam vinylpyrrolidone, vinylcaprolactam methacrylic acid methacrylic acid (C) at least two Formula (1), wherein R.sub.1 denotes Formula (I), wherein R.sub.1 denotes Formula (I), wherein Formula (I), wherein different hydrogen or methyl, n is a real hydrogen or methyl, n is a real R.sub.1 is methyl, R.sub.1 is methyl, monomers of number in the range of ≥10 number in the range of ≥10 n is a real number n is a real number formula (1) to ≤80, R.sub.2 denotes branched, to ≤70, R.sub.2 denotes branched, in the range of ≥10 in the range of ≥10 unsubstituted C.sub.10-C.sub.15 alkyl, and unsubstituted C.sub.10-C.sub.15 alkyl, and to ≤60, R.sub.2 denotes to ≤50, R.sub.2 denotes C.sub.10-C.sub.15 alkyl has an iso-index in C.sub.10-C.sub.15 alkyl has an iso-index in branched, branched, the range of ≥1.5 to ≤3.5 the range of ≥1.5 to ≤3.5 unsubstituted C.sub.10-C.sub.15 unsubstituted C.sub.10-C.sub.15 alkyl, and C.sub.10-C.sub.15 alkyl, and C.sub.10-C.sub.15 alkyl has an iso-index alkyl has an iso-index in the range of ≥1.8 in the range of ≥2 to ≤2.8 to ≤2.5 Optionally, (D) (D) is selected from the group (D) is selected from the group (D) is selected from (D) is selected from at least one consisting of ethylene glycol consisting of ethylene glycol the group consisting the group consisting cross linking diacrylate, ethylene glycol diacrylate, ethylene glycol of ethylene glycol of ethylene glycol reagent dimethacrylate, trimethylolpropane- dimethacrylate, trimethylolpropane- diacrylate, ethylene diacrylate, ethylene triacrylate, trimethylolpropanetri- triacrylate, trimethylolpropanetri- glycol dimethacrylate, glycol dimethacrylate, methacrylate, allyl acrylate, meth- methacrylate, allyl acrylate, meth- trimethylolpropane- trimethylolpropane- ylenebisacrylamide, meth- ylenebisacrylamide, meth- triacrylate, tri- triacrylate, tri- ylenebismethacrylamide, tetral- ylenebismethacrylamide, tetral- methylolpropanetri- methylolpropanetri- lyloxyethane, triallylcyanurates, lyloxyethane, triallylcyanurates, methacrylate, allyl methacrylate, allyl and allylic ethers of and allylic ethers of acrylate, meth- acrylate, meth- pentaerythritol, sorbitol, or pentaerythritol, sorbitol, or ylenebisacrylamide, ylenebisacrylamide, sucrose or diallylester of phthalic sucrose or diallylester of phthalic methylenebismeth- methylenebismeth- acid acid acrylamide, tetral- acrylamide, tetral- lyloxyethane, lyloxyethane, triallylcyanurates, triaIlyIcyanurates, and allylic ethers of and allylic ethers of pentaerythritol, pentaerythritol, sorbitol, or sucrose sorbitol, or sucrose or diallylester of or diallylester of phthalic acid phthalic acid Optionally, (E) (E) is selected from the group E) is selected from the group E) is selected from E) is selected from at least one consisting of linear, branched, consisting of linear, branched, the group consisting the group consisting ethylenically cycloaliphatic or arylaliphatic cycloaliphatic or arylaliphatic of linear, branched, of linear, branched, unsaturated esters of acrylic or methacrylic esters of acrylic or methacrylic cycloaliphatic or cycloaliphatic or monomer acids, isomers of butyl acids, isomers of butyl arylaliphatic esters arylaliphatic esters which is (meth)acrylate, isomers of hexyl (meth)acrylate, isomers of hexyl of acrylic or of acrylic or different (meth)acrylate, n-octyl (meth)acrylate, n-octyl methacrylic acids, methacrylic acids, from (A), (meth)acrylate, 2-ethylhexyl (meth)acrylate, 2-ethylhexyl isomers of butyl isomers of butyl (B), and (C) (meth)acrylate, 1-decyl (meth)acrylate, 1-decyl (meth)acrylate, (meth)acrylate, (meth)acrylate, 2-decyl (meth)acrylate, 2-decyl isomers of hexyl isomers of hexyl (meth)acrylate, isodecyl (meth)acrylate, isodecyl (meth)acrylate, (meth)acrylate, (meth)acrylate, isomers of (meth)acrylate, isomers of n-octyl (meth)acrylate, n-octyl (meth)acrylate, dodecyl (meth)acrylate, dodecyl (meth)acrylate, 2-ethylhexyl 2-ethylhexyl cyclohexyl (meth)acrylate, cyclohexyl (meth)acrylate, (meth)acrylate, 1-decyl (meth)acrylate, 1-decyl isobornyl (meth)acrylate, benzyl isobornyl (meth)acrylate, benzyl (meth)acrylate, 2-decyl (meth)acrylate, 2-decyl (meth)acrylate, vinylaromatic (meth)acrylate, vinylaromatic (meth)acrylate, isodecyl (meth)acrylate, isodecyl monomers, amide or nitrile monomers, amide or nitrile (meth)acrylate, isomers (meth)acrylate, isomers derivatives of (meth)acrylic acids derivatives of (meth)acrylic acids of dodecyl (meth)acrylate, of dodecyl (meth)acrylate, cyclohexyl (meth)acrylate, cyclohexyl (meth)acrylate, isobornyl (meth)acrylate, isobornyl (meth)acrylate, benzyl (meth)acrylate, benzyl (meth)acrylate, vinylaromatic monomers, vinylaromatic monomers, amide or nitrile amide or nitrile derivatives of derivatives of (meth)acrylic acids (meth)acrylic acids (F) optionally, (F) is selected from the group (F) is selected from the group (F) is selected from (F) is selected from at least one consisting of n-dodecyl consisting of n-dodecyl the group consisting the group consisting chain transfer mercaptan, n-decyl mercaptan, mercaptan, n-decyl mercaptan, of n-dodecyl mercaptan, of n-dodecyl mercaptan, agent octyl mercaptan, 1,8- dimercapto- octyl mercaptan, 1,8- dimercapto- n-decyl mercaptan, n-decyl mercaptan, 3, 6-dioxaoctane, thiolactic acid 3, 6-dioxaoctane, thiolactic acid octyl mercaptan, 1,8- octyl mercaptan, 1,8- and tert-dodecanthiol, 2- and tert-dodecanthiol, 2- dimercapto- 3, 6- dimercapto- 3, 6- (ethylhexyl)thioglycolate and (ethylhexyl)thioglycolate and dioxaoctane, and 2- dioxaoctane, and 2- terpinolene terpinolene (ethylhexyl)thioglycolate (ethylhexyl)thioglycolate
(55) TABLE-US-00003 TABLE 3 Component(s) i j k l (A) at least one (A) is selected from the group (A) is selected from the group (A) is selected from (A) is selected from ethylenically consisting of acrylic acid, consisting of acrylic acid, the group consisting of the group consisting of unsaturated methacrylic acid, C.sub.1 to C.sub.4 methacrylic acid, C.sub.1 to C.sub.4 acrylic acid, acrylic acid, monomer with monoesters of maleic or itaconic monoesters of maleic or itaconic methacrylic acid, methacrylic acid, a carboxylic acids, and mixtures thereof, or is acids, and mixtures thereof, or is C.sub.1 to C.sub.4 monoesters C.sub.1 to C.sub.4 monoesters function selected from the group consisting selected from the group consisting of maleic or itaconic of maleic or itaconic of ethylenically unsaturated of ethylenically unsaturated acids, and mixtures acids, and mixtures monomer with a carboxylic monomer with a carboxylic thereof thereof function, consisting of crotonic, function, consisting of crotonic, isocrotonic, cinnamic, itaconic, isocrotonic, cinnamic, itaconic, maleic acid, and maleic anhydride maleic acid, and maleic anhydride (B) at least one (B) is selected from the group (B) is selected from the group (B) is selected from (B) is selected from non-ionic consisting of methyl, ethyl, butyl consisting of methyl, ethyl, butyl the group consisting the group consisting ethylenically or 2-ethyl-hexyl esters of acrylic or 2-ethyl-hexyl esters of acrylic of methyl, ethyl, of methyl, ethyl, unsaturated and methacrylic acid, acrylonitrile, and methacrylic acid, acrylonitrile, butyl or 2-ethyl-hexyl butyl or 2-ethyl-hexyl monomer vinyl acetate, styrene, vinyl acetate, styrene, esters of acrylic, esters of acrylic, methylstyrene, diisobutylene, methylstyrene, diisobutylene, and methacrylic acid and methacrylic acid vinylpyrrolidone, vinylcaprolactam vinylpyrrolidone, vinylcaprolactam (C) at least one Formula (1), wherein R.sub.1 denotes Formula (I), wherein R.sub.1 denotes Formula (I), wherein Formula (I), wherein monomer of hydrogen or methyl, n is a real hydrogen or methyl, n is a real R.sub.1 is methyl, R.sub.1 is methyl, formula (1) number in the range of ≥10 number in the range of ≥10 n is a real number n is a real number to ≤80, R.sub.2 denotes branched, to ≤70, R.sub.2 denotes branched, in the range of ≥10 in the range of ≥10 unsubstituted C.sub.12-C.sub.15 alkyl, and unsubstituted C.sub.12-C.sub.15 alkyl, and to ≤60, R.sub.2 denotes to ≤50, R.sub.2 denotes C.sub.12-C.sub.15 alkyl has an iso-index in C.sub.12-C.sub.15 alkyl has an iso-index in branched, branched, the range of ≥1.5 to ≤3.5 the range of ≥1.5 to ≤3.5 unsubstituted C.sub.12-C.sub.15 unsubstituted C.sub.12-C.sub.15 alkyl, and C.sub.12-C.sub.15 alkyl, and C.sub.12-C.sub.15 alkyl has an iso-index alkyl has an iso-index in the range of ≥1.8 in the range of ≥2 to ≤2.8 to ≤2.5 Optionally, (D) (D) is selected from the group (D) is selected from the group (D) is selected from (D) is selected from at least one consisting of ethylene glycol consisting of ethylene glycol the group consisting the group consisting cross linking diacrylate, ethylene glycol diacrylate, ethylene glycol of ethylene glycol of ethylene glycol reagent dimethacrylate, trimethylolpropane- dimethacrylate, trimethylolpropane- diacrylate, ethylene diacrylate, ethylene triacrylate, trimethylolpropanetri- triacrylate, trimethylolpropanetri- glycol dimethacrylate, glycol dimethacrylate, methacrylate, allyl acrylate, meth- methacrylate, allyl acrylate, meth- trimethylolpropane- trimethylolpropane- ylenebisacrylamide, meth- ylenebisacrylamide, meth- triacrylate, tri- triacrylate, tri- ylenebismethacrylamide, tetral- ylenebismethacrylamide, tetral- methylolpropanetri- methylolpropanetri- lyloxyethane, triallylcyanurates, lyloxyethane, triallylcyanurates, methacrylate, allyl methacrylate, allyl and allylic ethers of and allylic ethers of acrylate, acrylate, pentaerythritol, sorbitol, or pentaerythritol, sorbitol, or methylenebisacrylamide, methylenebisacrylamide, sucrose or diallylester of phthalic sucrose or diallylester of phthalic methylenebismeth- methylenebismeth- acid acid acrylamide, tetral- acrylamide, tetral- lyloxyethane, tri- lyloxyethane, tri- allylcyanurates, allylcyanurates, and allylic ethers of and allylic ethers of pentaerythritol, pentaerythritol, sorbitol, or sucrose sorbitol, or sucrose or diallylester of or diallylester of phthalic acid phthalic acid Optionally, (E) (E) is selected from the group (E) is selected from the group (E) is selected from (E) is selected from at least one consisting of linear, branched, consisting of linear, branched, the group consisting the group consisting ethylenically cycloaliphatic or arylaliphatic cycloaliphatic or arylaliphatic of linear, branched, of linear, branched, unsaturated esters of acrylic or methacrylic esters of acrylic or methacrylic cycloaliphatic or cycloaliphatic or monomer acids, isomers of butyl acids, isomers of butyl arylaliphatic esters arylaliphatic esters which is (meth)acrylate, isomers of hexyl (meth)acrylate, isomers of hexyl of acrylic or of acrylic or different (meth)acrylate, n-octyl (meth)acrylate, n-octyl methacrylic acids, methacrylic acids, from (A), (meth)acrylate, 2-ethylhexyl (meth)acrylate, 2-ethylhexyl isomers of butyl isomers of butyl (B), and (C) (meth)acrylate, 1-decyl (meth)acrylate, 1-decyl (meth)acrylate, (meth)acrylate, (meth)acrylate, 2-decyl (meth)acrylate, 2-decyl isomers of hexyl isomers of hexyl (meth)acrylate, isodecyl (meth)acrylate, isodecyl (meth)acrylate, (meth)acrylate, (meth)acrylate, isomers of (meth)acrylate, isomers of n-octyl (meth)acrylate, n-octyl (meth)acrylate, dodecyl (meth)acrylate, dodecyl (meth)acrylate, 2-ethylhexyl 2-ethylhexyl cyclohexyl (meth)acrylate, cyclohexyl (meth)acrylate, (meth)acrylate, 1-decyl (meth)acrylate, 1-decyl isobornyl (meth)acrylate, benzyl isobornyl (meth)acrylate, benzyl (meth)acrylate, 2-decyl (meth)acrylate, 2-decyl (meth)acrylate, vinylaromatic (meth)acrylate, vinylaromatic (meth)acrylate, isodecyl (meth)acrylate, isodecyl monomers, amide or nitrile monomers, amide or nitrile (meth)acrylate, isomers (meth)acrylate, isomers derivatives of (meth)acrylic acids derivatives of (meth)acrylic acids of dodecyl (meth)acrylate, of dodecyl (meth)acrylate, cyclohexyl (meth)acrylate, cyclohexyl (meth)acrylate, isobornyl (meth)acrylate, isobornyl (meth)acrylate, benzyl (meth)acrylate, benzyl (meth)acrylate, vinylaromatic monomers, vinylaromatic monomers, amide or nitrile amide or nitrile derivatives of derivatives of (meth)acrylic acids (meth)acrylic acids (F) optionally, (F) is selected from the group (F) is selected from the group (F) is selected from (F) is selected from at least one consisting of n-dodecyl consisting of n-dodecyl the group consisting the group consisting chain transfer mercaptan, n-decyl mercaptan, mercaptan, n-decyl mercaptan, of n-dodecyl mercaptan, of n-dodecyl mercaptan, agent octyl mercaptan, 1,8- dimercapto- octyl mercaptan, 1,8- dimercapto- n-decyl mercaptan, n-decyl mercaptan, 3, 6-dioxaoctane, thiolactic acid 3, 6-dioxaoctane, thiolactic acid octyl mercaptan, 1,8- octyl mercaptan, 1,8- and tert-dodecanthiol, 2- and tert-dodecanthiol, 2- dimercapto-3, 6- dimercapto-3, 6- (ethylhexyl)thioglycolate and (ethylhexyl)thioglycolate and dioxaoctane, and 2- dioxaoctane, and 2- terpinolene terpinolene (ethylhexyl)thioglycolate (ethylhexyl)thioglycolate
(56) TABLE-US-00004 TABLE 4 Component(s) m n o p (A) at least one (A) is selected from the group (A) is selected from the group (A) is selected from (A) is selected from ethylenically consisting of acrylic acid, consisting of acrylic acid, the group consisting the group consisting unsaturated methacrylic acid, C.sub.1 to C.sub.4 methacrylic acid, C.sub.1 to C.sub.4 of acrylic acid, of acrylic acid, monomer with monoesters of maleic or itaconic monoesters of maleic or itaconic methacrylic acid, methacrylic acid, a carboxylic acids, and mixtures thereof, or is acids, and mixtures thereof, or is C.sub.1 to C.sub.4 monoesters C.sub.1 to C.sub.4 monoesters function selected from the group consisting selected from the group consisting of maleic or itaconic of maleic or itaconic of ethylenically unsaturated of ethylenically unsaturated acids, and mixtures acids, and mixtures monomer with a carboxylic monomer with a carboxylic thereof thereof function, consisting of crotonic, function, consisting of crotonic, isocrotonic, cinnamic, itaconic, isocrotonic, cinnamic, itaconic, maleic acid, and maleic anhydride maleic acid, and maleic anhydride (B) at least two (B) is selected from the group (B) is selected from the group (B) is selected from (B) is selected from different consisting of methyl, ethyl, butyl consisting of methyl, ethyl, butyl the group consisting the group consisting nonionic or 2-ethyl-hexyl esters of acrylic or 2-ethyl-hexyl esters of acrylic of methyl, ethyl, of methyl, ethyl, ethylenically and methacrylic acid, acrylonitrile, and methacrylic acid, acrylonitrile, butyl or 2-ethyl- butyl or 2-ethyl- unsaturated vinyl acetate, styrene, vinyl acetate, styrene, hexyl esters of hexyl esters of monomer methylstyrene, diisobutylene, methylstyrene, diisobutylene, acrylic, acrylic, vinylpyrrolidone, vinylcaprolactam vinylpyrrolidone, vinylcaprolactam methacrylic acid methacrylic acid (C) at least two Formula (1), wherein R.sub.1 denotes Formula (I), wherein R.sub.1 denotes Formula (I), wherein Formula (I), wherein different hydrogen or methyl, n is a real hydrogen or methyl, n is a real R.sub.1 is methyl, R.sub.1 is methyl, monomers of number in the range of ≥10 number in the range of ≥10 n is a real number n is a real number formula (1) to ≤80, R.sub.2 denotes branched, to ≤70, R.sub.2 denotes branched, in the range of ≥10 in the range of ≥10 unsubstituted C.sub.12-C.sub.15 alkyl, and unsubstituted C.sub.12-C.sub.15 alkyl, and to ≤60, R.sub.2 denotes to ≤50, R.sub.2 denotes C.sub.12-C.sub.15 alkyl has an iso-index in C.sub.12-C.sub.15 alkyl has an iso-index in branched, branched, the range of ≥1.5 to ≤3.5 the range of ≥1.5 to ≤3.5 unsubstituted C.sub.12-C.sub.15 unsubstituted C.sub.12-C.sub.15 alkyl, and C.sub.12-C.sub.15 alkyl, and C.sub.12-C.sub.15 alkyl has an iso-index alkyl has an iso-index in the range of ≥1.8 in the range of ≥2 to ≤2.8 to ≤2.5 Optionally, (D) (D) is selected from the group (D) is selected from the group (D) is selected from (D) is selected from at least one consisting of ethylene glycol consisting of ethylene glycol the group consisting the group consisting cross linking diacrylate, ethylene glycol diacrylate, ethylene glycol of ethylene glycol of ethylene glycol reagent dimethacrylate, trimethylolpropane- dimethacrylate, trimethylolpropane- diacrylate, ethylene diacrylate, ethylene triacrylate, trimethylolpropanetri- triacrylate, trimethylolpropanetri- glycol dimethacrylate, glycol dimethacrylate, methacrylate, allyl acrylate, meth- methacrylate, allyl acrylate, meth- trimethylolpropane- trimethylolpropane- ylenebisacrylamide, meth- ylenebisacrylamide, meth- triacrylate, tri- triacrylate, tri- ylenebismethacrylamide, tetral- ylenebismethacrylamide, tetral- methylolpropanetri- methylolpropanetri- lyloxyethane, triallylcyanurates, lyloxyethane, triallylcyanurates, methacrylate, allyl methacrylate, allyl and allylic ethers of and allylic ethers of acrylate, meth- acrylate, meth- pentaerythritol, sorbitol, or pentaerythritol, sorbitol, or ylenebisacrylamide, ylenebisacrylamide, sucrose or diallylester of phthalic sucrose or diallylester of phthalic methylenebismeth- methylenebismeth- acid acid acrylamide, tetral- acrylamide, tetral- lyloxyethane, tri- lyloxyethane, tri- allylcyanurates, allylcyanurates, and allylic ethers of and allylic ethers of pentaerythritol, pentaerythritol, sorbitol, or sucrose sorbitol, or sucrose or diallylester of or diallylester of phthalic acid phthalic acid Optionally, (E) (E) is selected from the group (E) is selected from the group (E) is selected from (E) is selected from at least one consisting of linear, branched, consisting of linear, branched, the group consisting the group consisting ethylenically cycloaliphatic or arylaliphatic cycloaliphatic or arylaliphatic of linear, branched, of linear, branched, unsaturated esters of acrylic or methacrylic esters of acrylic or methacrylic cycloaliphatic or cycloaliphatic or monomer acids, isomers of butyl acids, isomers of butyl arylaliphatic esters arylaliphatic esters which is (meth)acrylate, isomers of hexyl (meth)acrylate, isomers of hexyl of acrylic or of acrylic or different (meth)acrylate, n-octyl (meth)acrylate, n-octyl methacrylic acids, methacrylic acids, from (A), (meth)acrylate, 2-ethylhexyl (meth)acrylate, 2-ethylhexyl isomers of butyl isomers of butyl (B), and (C) (meth)acrylate, 1-decyl (meth)acrylate, 1-decyl (meth)acrylate, (meth)acrylate, (meth)acrylate, 2-decyl (meth)acrylate, 2-decyl isomers of hexyl isomers of hexyl (meth)acrylate, isodecyl (meth)acrylate, isodecyl (meth)acrylate, (meth)acrylate, (meth)acrylate, isomers of (meth)acrylate, isomers of n-octyl (meth)acrylate, n-octyl (meth)acrylate, dodecyl (meth)acrylate, dodecyl (meth)acrylate, 2-ethylhexyl 2-ethylhexyl cyclohexyl (meth)acrylate, cyclohexyl (meth)acrylate, (meth)acrylate, 1-decyl (meth)acrylate, 1-decyl isobornyl (meth)acrylate, benzyl isobornyl (meth)acrylate, benzyl (meth)acrylate, 2-decyl (meth)acrylate, 2-decyl (meth)acrylate, vinylaromatic (meth)acrylate, vinylaromatic (meth)acrylate, isodecyl (meth)acrylate, isodecyl monomers, amide or nitrile monomers, amide or nitrile (meth)acrylate, isomers (meth)acrylate, isomers derivatives of (meth)acrylic acids derivatives of (meth)acrylic acids of dodecyl (meth)acrylate, of dodecyl (meth)acrylate, cyclohexyl (meth)acrylate, cyclohexyl (meth)acrylate, isobornyl (meth)acrylate, isobornyl (meth)acrylate, benzyl (meth)acrylate, benzyl (meth)acrylate, vinylaromatic monomers, vinylaromatic monomers, amide or nitrile amide or nitrile derivatives of derivatives of (meth)acrylic acids (meth)acrylic acids (F) optionally, (F) is selected from the group (F) is selected from the group (F) is selected from (F) is selected from at least one consisting of n-dodecyl consisting of n-dodecyl the group consisting the group consisting chain transfer mercaptan, n-decyl mercaptan, mercaptan, n-decyl mercaptan, of n-dodecyl mercaptan, of n-dodecyl mercaptan, agent octyl mercaptan, 1,8- dimercapto- octyl mercaptan, 1,8- dimercapto- n-decyl mercaptan, n-decyl mercaptan, 3, 6-dioxaoctane, thiolactic acid 3, 6-dioxaoctane, thiolactic acid octyl mercaptan, 1,8- octyl mercaptan, 1,8- and tert-dodecanthiol, 2- and tert-dodecanthiol, 2- dimercapto-3, 6- dimercapto-3, 6- (ethylhexyl)thioglycolate and (ethylhexyl)thioglycolate and dioxaoctane, and 2- dioxaoctane, and 2- terpinolene terpinolene (ethylhexyl)thioglycolate (ethylhexyl)thioglycolate
(57) Preferred variants 1 to 7 of the embodiments a to p are summarized in the Table 5.
(58) TABLE-US-00005 TABLE 5 Component(s) 1 2 3 4 5 6 7 (A) ≥30 wt.-% ≥33 wt.-% ≥36 wt.-% ≥36 wt.-% ≥38 wt.-% ≥38 wt.-% ≥38 wt.-% to ≤70 wt.-% to ≤67 wt.-% to ≤64 wt.-% to ≤55 wt.-% to ≤55 wt.-% to ≤50 wt.-% to ≤45 wt.-% (B) ≥30 wt.-% ≥33 wt.-% ≥36 wt.-% ≥40 wt.-% ≥42 wt.-% ≥45 wt.-% ≥45 wt.-% to ≤70 wt.-% to ≤67 wt.-% to ≤64 wt.-% to ≤60 wt.-% to ≤58 wt.-% to ≤55 wt.-% to ≤55 wt.-% (C) ≥1 wt.-% ≥4 wt.-% ≥8 wt.-% ≥8 wt.-% ≥8 wt.-% ≥8 wt.-% ≥8 wt.-% to ≤40 wt.-% to ≤30 wt.-% to ≤30 wt.-% to ≤30 wt.-% to ≤25 wt.-% to ≤20 wt.-% to ≤20 wt.-% (D) ≥0 wt.-% ≥0 wt.-% ≥0 wt.-% ≥0 wt.-% ≥0 wt.-% ≥0 wt.-% ≥0 wt.-% to ≤1 wt.-% to ≤0.8 wt.-% to ≤0.6 wt.-% to ≤0.6 wt.-% to ≤0.5 wt.-% to ≤0.5 wt.-% to ≤0.4 wt.-% (E) ≥0 wt.-% ≥0 wt.-% ≥0 wt.-% ≥0 wt.-% ≥0 wt.-% ≥0 wt.-% ≥0 wt.-% to ≤10 wt.-% to ≤9 wt.-% to ≤8 wt.-% to ≤7 wt.-% to ≤6 wt.-% to ≤5 wt.-% to ≤5 wt.-% (F) ≥0 wt.-% ≥0 wt.-% ≥0 wt.-% ≥0 wt.-% ≥0 wt.-% ≥0 wt.-% ≥0 wt.-% to ≤1 wt.-% to ≤0.9 wt.-% to ≤0.8 wt.-% to ≤0.7 wt.-% to ≤0.6 wt.-% to ≤0.5 wt.-% to ≤0.5 wt.-%
(59) Preferred copolymer results from the following combinations of the embodiments a to p with variants 1 to 7: a.sup.1, a.sup.2, a.sup.3, a.sup.4, a.sup.5, a.sup.6, a.sup.7, b.sup.1, b.sup.2, b.sup.3, b.sup.4, b.sup.5, b.sup.6, b.sup.7, c.sup.1, c.sup.2, c.sup.3, c.sup.4, c.sup.5, c.sup.6, c.sup.7, d.sup.1, d.sup.2, d.sup.3, d.sup.4, d.sup.5, d.sup.6, d.sup.7, e.sup.1, e.sup.2, e.sup.3, e.sup.4, e.sup.5, e.sup.6, e.sup.7, f.sup.1, f.sup.2, f.sup.3, f.sup.4, f.sup.5, f.sup.6, f.sup.7, g.sup.1, g.sup.2, g.sup.3, g.sup.4, g.sup.5, g.sup.6, g.sup.7, h.sup.1, h.sup.2, h.sup.3, h.sup.4, h.sup.5, h.sup.6, h.sup.7, i.sup.1, i.sup.2, i.sup.3, i.sup.4, i.sup.5, i.sup.6, i.sup.7, j.sup.1, j.sup.2, j.sup.3, j.sup.4, j.sup.5, j.sup.6, j.sup.7, k.sup.1, k.sup.2, k.sup.3, k.sup.4, k.sup.5, k.sup.6, k.sup.7, l.sup.1, l.sup.2, l.sup.3, l.sup.4, l.sup.5, l.sup.6, l.sup.7, m.sup.1, m.sup.2, m.sup.3, m.sup.4, m.sup.5, m.sup.6, m.sup.7, n.sup.1, n.sup.2, n.sup.3, n.sup.4, n.sup.5, n.sup.6, n.sup.7, o.sup.1, o.sup.2, o.sup.3, o.sup.4, o.sup.5, o.sup.6, o.sup.7, p.sup.1, p.sup.2, p.sup.3, p.sup.4, p.sup.5, p.sup.6, p.sup.7. For example “a.sup.1” means a combination of embodiment “a” with variant “1”, i.e a copolymer containing ≥30 wt.-% to 70 wt.-% of at least one ethylenically unsaturated monomer with a carboxylic function (A) selected from the group consisting of acrylic acid, methacrylic acid, C.sub.1 to C.sub.4 monoesters of maleic or itaconic acids, and mixtures thereof, or is selected from the group consisting of ethylenically unsaturated monomer with a carboxylic function, consisting of crotonic, isocrotonic, cinnamic, itaconic, maleic acid, and maleic anhydride, 30 wt.-% to ≤70 wt.-% of at least one non-ionic ethylenically unsaturated monomer (B) selected from the group consisting of methyl, ethyl, butyl or 2-ethyl-hexyl esters of acrylic and methacrylic acid, acrylonitrile, vinyl acetate, styrene, methylstyrene, diisobutylene, vinylpyrrolidone, vinylcaprolactam, 1 wt.-% to ≤40 wt.-% of at least one monomer (C) of formula (I) wherein R.sub.1 denotes hydrogen or methyl, n is a real number in the range of ≥10 to ≤80, R.sub.2 denotes branched, unsubstituted C.sub.10-C.sub.15alkyl, and C.sub.10-C.sub.15 alkyl has an iso-index in the range of ≥1.5 to ≤3.5, optionally, ≥0 wt.-% to ≤1 wt.-% of at least one cross linking reagent (D) selected from the group consisting of ethylene glycol diacrylate, ethylene glycol dimethacrylate, trimethylolpropanetriacrylate, trimethylolpropanetrimethacrylate, allyl acrylate, methylenebisacrylamide, methylenebismethacrylamide, tetrallyloxyethane, triallylcyanurates, and allylic ethers of pentaerythritol, sorbitol, or sucrose or diallylester of phthalic acid, optionally, ≥0 wt.-% to ≤10 wt.-% of at least one ethylenically unsaturated monomer (E) which is different from (A), (B), and (C), selected from the group consisting of linear, branched, cycloaliphatic or arylaliphatic esters of acrylic or methacrylic acids, isomers of butyl (meth)acrylate, isomers of hexyl (meth)acrylate, n-octyl (meth)acrylate, 2-ethylhexyl (meth)acrylate, 1-decyl (meth)acrylate, 2-decyl (meth)acrylate, isodecyl (meth)acrylate, isomers of dodecyl (meth)acrylate, cyclohexyl (meth)acrylate, isobornyl (meth)acrylate, benzyl (meth)acrylate, vinylaromatic monomers, amide or nitrile derivatives of (meth)acrylic acids, and optionally, ≥0 wt.-% to ≤1 wt.-% of at least one chain transfer agent (F) selected from the group consisting of n-dodecyl mercaptan, n-decyl mercaptan, octyl mercaptan, 1,8-dimercapto-3,6-dioxaoctane, thiolactic acid and tert-dodecanthiol, 2-(ethylhexyl)thioglycolate and terpinolene.
(60) The copolymer according to the present invention has the following advantages: 1. Effective thickener at high shear rates and creates a Newtonian rheology profile in aqueous coating formulations. 2. Environment friendly as it does not contain tin, APEO (alkylphenolethoxylate) and low amounts of volatile organic compounds. 3. Stability of rheology upon storage and compatibility with colorants.
(61) Having generally described the invention, a further understanding can be obtained by reference to certain specific examples which are provided herein for the purpose of illustration only, and are not intended to be limiting unless otherwise specified.
EXAMPLES
Compounds
(62) Chain transfer agent 1 (N-dodecylmercaptane),
(63) Chain transfer agent 2-(ethylhexyl)thioglycolate),
(64) Initiator 1 (Ammoniumpersulphate),
(65) Initiator 2 (Sodiumpersulphate),
(66) Ammonia and ammonium hydroxide are used as neutralising agent, and are available from Sigma Aldrich.
(67) Ethyl acrylate, acrylic acid esters,
(68) Methacrylic acid, unsaturated monocarboxylic acid,
(69) Methyl methacrylate, methyl ester of acrylic acid,
(70) Surfactant A (Disponil® FES 993), fatty alcohol, polyglycol ether sulphate, Na salt,
(71) Surfactant B (Disponil® FES 77), 32% active anionic surfactant Sodium lauryl ether sulfate,
(72) Surfactant C (Disponil® FES 27), 28% active anionic surfactant Sodium lauryl ether sulfate,
(73) Surfactant D (Disponil SDS) 15% active anionic surfactant, Sodiumdodecylsulfate
(74) Hydropalat® WE3240, an organic modified polysiloxane (silicone surfactant) dissolved in dipropylene glycol mono methyl ether, used as a wetting agent,
(75) Dispex® CX 4320, a polycarboxylate copolymer sodium salt, used as pigment dispersing agent,
(76) Solvenon® DPM, a mixture of isomers dipropylene glycol monomethyl ether, methoxypropoxy-propanol, methyldipropylene glycol which is used as a film forming agent,
(77) Acronal® DS 6277, an acrylic latex polymer, used as a binder,
(78) FoamStar® SI2210, a mixture of specially modified alcohols and a polysiloxane adduct, used as a defoamer,
(79) FoamStar® ST 2438, defoamer based on organo-modified polysiloxanes and hyper-branched star polymer, and
(80) Acronal® Plus 4130, an acrylic latex, used as a binder, are available from BASF SE, Ludwigshafen, Germany.
(81) Kronos® 2190 is titanium oxide, available from Kronos.
(82) Finntalc® M15 is a talc (Mg-Silicate), available from Mondo Minerals B.V.
(83) TiPure® R 706 is a titanium oxide pigment, available from The Chemours Company TT, LLC.
(84) Texanol® is an ester alcohol used as a film forming agent, available from Eastman Chemical Company.
Methods
(85) The mean degree of branching determined was by .sup.1H NMR spectroscopy by the method as follows:
(86) A sample of the alcohol R.sup.2—OH, used for the preparation of the monomer (C), was first derivatized with trichloroacetyl isocyanate (TAI) (J. Loccufier et al., Polymer Bulletin 27, 1991, 201). The signals of the esterified primary alcohols are situated at δ=4.7 to 4.0 ppm, those of the esterified secondary alcohols (if present) at about 5 ppm, and water present in the sample reacts with TAI to give carbamic acid. All methyl, methylene and methine protons are situated in the range from 2.4 to 0.4 ppm. The signals <1 ppm here are assigned to the methyl groups. From the spectrum obtained in this way, the mean degree of branching (iso index) may be calculated as follows:
Iso index (Ix)=((F(CH.sub.3)/3)/(F(CH.sub.2—OH)/2))−1
where F(CH.sub.3) represents the signal area corresponding to the methyl protons, and F(CH.sub.2—OH) represents the signal area of the methylene protons in the CH.sub.2—OH group.
(87) Newtonian index was determined to demonstrate if the rheological profile is rather Newtonian or more pseudoplastic. To calculate the Newtonian index the low shear viscosity at 1 s.sup.−1 was divided by the high shear viscosity at a shear rate of 10000 s.sup.−1. The lower the value of the Newtonian index more Newtonian the rheological profile is expected. The rheological profile was determined with an “Anton Paar MCR 302” rheometer with a cone-plate geometry of 25 mm diameter (cone angle 1°) between a shear rate of 0.1 and 10000 s.sup.−1.
Emulsion Polymerization
(88) Comminution may be achieved by using high shear force dispersion devices, for example a ultrasonic sound equipment (J. Dispersion Sci. Technology 2002, 23(1-3), 333-349) or a high pressure homogenizer (APV Gaulin homogenizer; Microfluidizer) The emulsification and comminution can be carried out continuously or batchwise. Apparatus for this purpose are known in the art. This is for example described in U.S. Pat. No. 5,108,654.
Synthesis of Monomer (C) of Formula (I)
(89) The monomer (C) of formula (I) according to the present invention and monomer not within the scope of the invention were synthesized according to standard literature procedures from corresponding ethoxylates of technical alcohols. For example, DE10218752 describes the method of preparation of alkoxylate mixtures by reacting alkanols with alkylene oxides in the presence of a catalyst under alkoxylation conditions, which is followed by methacrylate synthesis. For example, M-01 corresponds to a monomer (C) which is out of the scope of the invention and is based on the commercial alcohol Lial® 123. This monomer was obtained by ethoxylation of Lial® 123 and then made polymerisable by functionalisation using a methacrylate group. Methacrylate synthesis was carried out using general procedures known in the art. For example, 1000 g alcohol ethoxylate (EO40) was charged into the reactor and stirred at 130° C. under vacuum for 3 h and then cool down to 80° C. Lean air is applied, and then 110 g methacrylic anhydride and 0.3 g butylhydroxytoluol was added. The mixture was keep at 80° C. for 15 hr and cooled down. All other monomers were derived from technical grade alcohols as starting material, which always comprise isomer mixtures. Table 6 provides the monomer (C) of formula (I) and monomer not within the scope of the invention which were used in the synthesis of HASE copolymer according to the present invention and HASE polymers which are not within the scope of the invention, respectively.
(90) TABLE-US-00006 TABLE 6 Iso index Monomer R.sub.1 n C- number (Ix) *M-01 methacrylate 40 C.sub.12/C.sub.13 0.6 *M-02 methacrylate 40 C.sub.12 1 *M-03 methacrylate 40 C.sub.12/C.sub.13 1 M-04 methacrylate 40 C.sub.12/C.sub.13 1.5 .sup. M-04′ methacrylate 40 C.sub.13 2 M-05 methacrylate 40 C.sub.13 2.4 M-06 methacrylate 40 C.sub.12/C.sub.13 2.4 M-07 methacrylate 40 C.sub.13 3 *M-08 methacrylate 20 C.sub.12/C.sub.13 0.6 *M-09 methacrylate 20 C.sub.12/C.sub.13 1 *M-10 methacrylate 20 C.sub.12 1 M-11 methacrylate 20 C.sub.12/C.sub.13 1.5 .sup. M-11′ methacrylate 20 C.sub.12/C.sub.13 2 M-12 methacrylate 20 C.sub.13 2.4 M-13 methacrylate 20 C.sub.13 2.4 M-14 methacrylate 20 C.sub.12/C.sub.13 3 M-15 methacrylate 30 C.sub.10/C.sub.13 1.7 M-16 methacrylate 40 C.sub.10/C.sub.13 1.7 *= not within the scope of the invention
Synthesis of HASE Copolymers
(91) The HASE copolymer samples were obtained by standard emulsion polymerisation methods. Two non-limiting examples of such methods are provided as procedures 1, 2 and 3.
Procedure 1
(92) 50.9 wt.-% of water, 70.6 wt.-% of solid surfactant A, monomers and chain transfer agent were weighed into the monomer emulsion feed vessel. 42.7 wt.-% of water and 29.4 wt.-% of surfactant was weighed into the polymerization vessel and heated to 85° C. Initiator was dissolved in 6.4 wt.-% water and placed into the initiator feed vessel. 5 wt.-% of the monomer emulsion was added into the polymerization vessel, afterwards 30 wt.-% of the initiator solution was added. The monomer emulsion was fed into the polymerization vessel within 120 minutes and in parallel, the remaining initiator solution was added in 150 minutes. After the end of both feeds the product was stirred for an additional hour at 85° C., cooled down and filtered to obtain the copolymer sample. The wt.-% is related to the total weight of the individual components ie. water, monomers, solid surfactant A, chain transfer agent, initiator.
Procedure 2
(93) 18.3 wt.-% of water, solid surfactant B, monomers and chain transfer agent were weight into the monomer emulsion feed vessel. 80.6 wt.-% of water and solid surfactant C was weight into the polymerization vessel and heated to 85° C. Initiator was dissolved in 1.1 wt.-% water and placed into the initiator feed vessel. 5 wt.-% of the monomer emulsion was added into the polymerization vessel, afterwards the initiator solution was added. The monomer emulsion was fed parallel into the polymerization vessel within 120 minutes. After the end of both feeds the product was stirred for an additional hour at 85° C., cooled down and filtered to obtain the copolymer sample. The wt.-% is related to the total weight of the individual components ie. water, monomers, solid surfactant B, solid surfactant C, chain transfer agent, initiator.
Procedure 3
(94) 50.5 wt.-% of water, 70 wt.-% of solid surfactant D and B, monomers and chain transfer agent were weight into the monomer emulsion feed vessel. 48.3 wt.-% of water and 30 wt.-% of surfactant D and B was weight into the polymerization vessel and heated to 85° C. Initiator was dissolved in 1.2 wt.-% water and placed into the initiator feed vessel. 5 wt.-% of the monomer emulsion was added into the polymerization vessel, afterwards 30 wt.-% of the initiator solution was added. The monomer emulsion was fed into the polymerization vessel within 120 minutes and in parallel, the remaining initiator solution was added in 150 minutes. After the end of both feeds the product was stirred for an additional hour at 85° C., cooled down and filtered to obtain the copolymer sample. The wt.-% is related to the total weight of the individual components ie. water, monomers, solid surfactant B, solid surfactant D, chain transfer agent, initiator.
(95) Table 7 provides the HASE copolymer examples 1 to 14 prepared by following the method of procedure 1.
(96) TABLE-US-00007 TABLE 7 Compounds Meth Methyl Chain Ethyl acrylic meth transfer Water Surfactant A acrylate acid acrylate Monomer (C) agent 1 Initiator 1 Example (in g) (in g) (in g) (in g) (in g) (in g) (in g) (in g) 01* 759 20 250 204 31 M-01: 25 1.3 1.3 02* 759 20 250 204 31 M-02: 25 1.3 1.3 03* 759 20 250 204 31 M-03: 25 1.3 1.3 04 759 20 250 204 31 M-04: 25 1.3 1.3 04′ 759 20 250 204 31 M-04′: 25 1.3 1.3 05 759 20 250 204 31 M-05: 25 1.3 1.3 06 759 20 250 204 31 M-06: 25 1.3 1.3 07 759 20 250 204 31 M-07: 25 1.3 1.3 08* 759 20 225 204 31 M-01: 50 1.3 1.3 09* 759 20 225 204 31 M-02: 50 1.3 1.3 10* 759 20 225 204 31 M-03: 50 1.3 1.3 11 759 20 225 204 31 M-04: 50 1.3 1.3 11′ 759 20 225 204 31 M-04′: 50 1.3 1.3 12 759 20 225 204 31 M-05: 50 1.3 1.3 13 759 20 225 204 31 M-06: 50 1.3 1.3 14 759 20 225 204 31 M-07: 50 1.3 1.3 *= not within the scope of the invention
(97) Table 8 provides the HASE copolymer examples 15 to 21 prepared by following the method of procedure 2 and varying the amount of varying the amounts of ethylacrylate and monomer (C).
(98) TABLE-US-00008 TABLE 8 Compounds Chain Surfactant(s) Ethyl Meth acrylic Methyl meth transfer Water B and C acrylate acid acrylate Monomer (C) agent Initiator 2 Example (in g) (in g) (in g) (in g) (in g) (in g) 2 (in g) (in g) 15* 1289 B: 8.6 223 178 0 M-01: 45 1.1 1.1 C: 8.6 16* 1289 B: 8.6 223 178 0 M-02: 45 1.1 1.1 C: 8.6 17* 1289 B: 8.6 223 178 0 M-03: 45 1.1 1.1 C: 8.6 18 1289 B: 8.6 223 178 0 M-04: 45 1.1 1.1 C: 8.6 18′ 1289 B: 8.6 223 178 0 M-04′: 45 1.1 1.1 C: 8.6 19 1289 B: 8.6 223 178 0 M-05: 45 1.1 1.1 C: 8.6 20 1289 B: 8.6 223 178 0 M-06: 45 1.1 1.1 C: 8.6 21 1289 B: 8.6 223 178 0 M-07: 45 1.1 1.1 C: 8.6 *= not within the scope of the invention
(99) Table 9a provides the HASE copolymer examples 22 to 28 prepared by following the method of procedure 1, by varying the amounts of ethylacrylate and monomer (C).
(100) TABLE-US-00009 TABLE 9 (a) Compounds Meth Methyl Chain Surfactant Ethyl acrylic meth transfer Water (A) acrylate acid acrylate Monomer (C) agent 1 Initiator 1 example (in g) (in g) (in g) (in g) (in g) (in g) (in g) (in g) 22* 759 20 200 204 31 MM-01: 75 1.3 1.3 23* 759 20 200 204 31 MM-02: 75 1.3 1.3 24* 759 20 200 204 31 MM-03: 75 1.3 1.3 25 759 20 200 204 31 MM-04: 75 1.3 1.3 25′ 759 20 200 204 31 MM-04′: 75 1.3 1.3 26 759 20 200 204 31 MM-05: 75 1.3 1.3 27 759 20 200 204 31 MM-06: 75 1.3 1.3 28 759 20 200 204 31 MM-07: 75 1.3 1.3 *= not within the scope of the invention
(101) Table 9b provides the HASE copolymer examples 29 to 34 prepared by following the method of procedure 3, by varying the amounts of ethylacrylate and monomer (C).
(102) TABLE-US-00010 TABLE 9 (b) Compounds Meth Methyl Chain Surfactant(s) Ethyl acrylic meth transfer Water B and D acrylate acid acrylate Monomer (C) agent 1 Initiator 2 example (in g) (in g) (in g) (in g) (in g) (in g) (in g) (in g) 29 766.4 B: 3.2 159.3 127.4 0 M-16: 31.8 0.8 0.8 D: 1.6 30 766.4 B: 3.2 143.3 127.4 0 M-11: 47.8 0.8 0.8 D: 1.6 31 766.4 B: 3.2 143.3 127.4 0 M-16: 47.8 0.8 0.8 D: 1.6 32 766.4 B: 3.2 143.3 127.4 0 M-15: 47.8 0.8 0.8 D: 1.6 33 766.4 B: 3.2 143.3 127.4 0 M-13: 47.8 0.8 0.8 D: 1.6 34 766.4 B: 3.2 143.3 127.4 0 M-14: 47.8 0.8 0.8 D: 1.6
(103) A coating formulation was prepared to demonstrate that the copolymer of the present invention is more efficient as a thickener in the high shear range (1000 s.sup.−1 to 10000 s.sup.−1) and exhibit a more Newtonian rheological profile than the state of art which is represented by the examples which are not within the scope of the invention.
(104) A wood coating formulation was prepared by adding 1 g of the copolymer example mentioned in Table 7, 8, 9 (a) and 9 (b), at an adjusted solids content of 25%, into 99 g of the coating formulation mentioned in table 10 below, under stirring. The resulting samples were stored over night at room temperature and then the rheological profile was determined. Newtonian index was determined to demonstrate that the rheological profile of coating formulation with the copolymer according to the present invention is more Newtonian than pseudoplastic.
(105) TABLE-US-00011 TABLE 10 Compound Purpose Quantity [g] Water solvent 306.1 Ammonia conc. neutralising agent 1.5 Hydropalat ® WE3240 wetting agent 1.5 FoamStar ® Si2210 defoamer 4.6 Dispex ® CX 4320 dispersant 9.2 Solvenon ® DPM film forming agent 30.6 Kronos ® 2190 titanium dioxide 336.7 Finntalc ® M15 filler 76.5 Acronal ® DS 6277 binder 727.0 FoamStar ® SI2210 defoamer 6.1
(106) The viscosity at high shear range (1000 s.sup.−1 to 10000 s−.sup.1) and Newtonian index were determined for the wood coating formulation. The viscosity values are provided in mPas.
(107) For comparison, examples which are not within the scope of the invention ie. 01*, 08*, 15*, 17*, 22* and 24* differing in the amounts of components (eg. ethyl acrylate and monomer (C)), were 20 compared with copolymer according to the present invention wherein same amount of different components has been used. The results obtained have been provided in Table 11 (a) to 11 (d).
(108) For example, example 01* has been compared with example 04′ and 07, and results are provided as below:
(109) TABLE-US-00012 TABLE 11 (a) Newtonian Iso-index 1 s.sup.−1 10 s.sup.−1 100 s.sup.−1 1000 s.sup.−1 10000 s.sup.−1 index Example (Ix) (mPas) (mPas) (mPas) (mPas) (mPas) (1 s.sup.−1/10000 s.sup.−1) 01* 0.6 24500 10400 3710 1020 194 126 04′ 2 22400 10100 3830 1100 219 102 07 3 19000 8740 3400 1020 215 88 *= not within the scope of the invention
(110) Example 08* has been compared with example 11′, 12 and 14 and, results are provided as below:
(111) TABLE-US-00013 TABLE 11 (b) Newtonian Iso-index 1 s.sup.−1 10 s.sup.−1 100 s.sup.−1 1000 s.sup.−1 10000 s.sup.−1 index Example (Ix) (mPas) (mPas) (mPas) (mPas) (mPas) (1 s.sup.−1/10000 s.sup.−1) 08* 0.6 28700 10300 3170 843 164 175 11′ 2 16500 7040 2720 904 193 85 12 2.4 28500 11200 4040 1190 227 126 14 3 14700 6370 2410 789 180 82 *= not within the scope of the invention
(112) For example, example 15* and 17* have been compared with example 19, 20 and 21 and results are provided as below:
(113) TABLE-US-00014 TABLE 11 (c) Newtonian Iso-index 1 s.sup.−1 10 s.sup.−1 100 s.sup.−1 1000 s.sup.−1 10000 s.sup.−1 index Example (Ix) (mPas) (mPas) (mPas) (mPas) (mPas) (1 s.sup.−1/10000 s.sup.−1) 15* 0.6 18710 7241 2386 672 139 135 17* 1 15560 6369 2219 660 137 114 19 2.4 11870 5588 2210 732 155 77 20 2.4 11470 5145 1963 643 144 79 21 3 9487 4386 1711 583 139 68 *= not within the scope of the invention
(114) For example, example 22* and 24* have been compared with example 25, 25′, 26, 27, 28, 30, 31, 32, 33 and 34 and results are provided as below:
(115) TABLE-US-00015 TABLE 11 (d) Newtonian Iso-index 1 s.sup.−1 10 s.sup.−1 100 s.sup.−1 1000 s.sup.−1 10000 s.sup.−1 index Example (Ix) (mPas) (mPas) (mPas) (mPas) (mPas) (1 s.sup.−1/10000 s.sup.−1) 22* 0.6 56100 15900 3700 785 125 449 24* 1 58000 16000 3810 821 132 439 25 1.5 53900 16100 3860 834 137 393 25′ 2 30700 12200 3600 883 152 202 26 2.4 46500 16900 4540 1030 158 294 27 2.4 45700 15100 3800 844 142 322 28 3 29800 10400 2930 712 134 222 30 1.5 37400 12500 3290 751 138 271 31 1.7 16100 6790 2390 676 128 126 32 1.7 26600 9760 2960 732 133 200 33 2.4 30000 10700 2990 707 137 219 34 3 26800 9950 2900 706 139 193
(116) An architectural interior paint formulation was prepared by diluting 1 g of the copolymer example mentioned in Table 7, 8, 9 (a) and 9 (b) at an adjusted solids content of 25%, with 1 g water and adding it into 97 g of the coating formulation mentioned in Table 12 below, under stirring. The remaining polymer in the dilution glass vial was rinsed with additional 1 g of water and also added to the formulation. The resulting samples were stored over night at room temperature and then the rheological profile was determined. Newtonian index was determined to demonstrate that the rheological profile of coating formulation with the copolymer according to the present invention is more Newtonian than pseudoplastic.
(117) TABLE-US-00016 TABLE 12 Compound Purpose Quantity [g] Water solvent 602.7 Ammonium hydroxide neutralising agent 2.0 Dispex ® CX 4320 dispersant 26.1 Foamstar ® ST 2438 defoamer 4.0 TiPure ® R 706 titanium dioxide 452.4 Foamstar ® ST 2438 defoamer 4.0 Texanol ® film forming agent 4.0 Acronal ® Plus 4130 binder 904.7
(118) The viscosity at high shear range (1000 s.sup.−1 to 10000 s.sup.−1) and Newtonian index were determined for the architectural interior paint formulation. The viscosity values are provided in mPas.
(119) For comparison, examples which are not within the scope of the invention ie. 08*, 10*, 15*, 17*, 22*, differing in the amounts of components (e.g. ethyl acrylate and monomer (C)), were compared with copolymer according to the present invention wherein same amount of different components has been used. The results obtained have been provided in Table 13 (a) to 13 (c).
(120) For example, example 08* and 10* have been compared with example 11′, 12, 13 and 14, and results are provided as below:
(121) TABLE-US-00017 TABLE 13 (a) Newtonian Ix 1 s.sup.−1 10 s.sup.−1 100 s.sup.−1 1000 s.sup.−1 10000 s.sup.−1 index Example (mPas) (mPas) (mPas) (mPas) (mPas) (mPas) (1 s.sup.−1/ 10000 s.sup.−1) 08* 0.6 1590 532 214 96 33 48 10* 1 1589 520 212 99 34 46 11′ 2 1173 430 194 100 39 30 12 2.4 1161 423 190 103 39 29 13 2.4 1273 442 188 94 35 36 14 3 1228 418 176 88 36 34 *= not within the scope of the invention
(122) For example, example 15* and 17* have been compared with example 18′, 19, 20 and 29, and results are provided as below:
(123) TABLE-US-00018 TABLE 13 (b) Newtonian Ix 1 s.sup.−1 10 s.sup.−1 100 s.sup.−1 1000 s.sup.−1 10000 s.sup.−1 index Example (mPas) (mPas) (mPas) (mPas) (mPas) (mPas) (1 s.sup.−1/10000 s.sup.−1) 15* 0.6 1216 559 292 122 38 32 17* 1 1251 564 294 124 40 32 18′ 2 662 347 197 104 41 16 19 2.4 819 443 273 138 45 18 20 2.4 1062 510 295 130 43 25 29 1.7 380 259 164 99 40 9 *= not within the scope of the invention
(124) For example, example 22* has been compared with example 25, 25′, 26, 27, 28, 30, 31 and 32, and results are provided as below:
(125) TABLE-US-00019 TABLE 13 (c) Newtonian Ix 1 s.sup.−1 10 s.sup.−1 100 s.sup.−1 1000 s.sup.−1 10000 s.sup.−1 index Example (mPas) (mPas) (mPas) (mPas) (mPas) (mPas) (1 s.sup.−1/10000 s.sup.−1) 22* 0.6 1805 645 273 117 39 46 25 1.5 1804 697 318 133 44 41 25′ 2 1138 410 190 102 39 29 26 2.4 1242 465 228 121 43 29 27 2.4 1673 666 317 137 46 36 28 3 1275 480 228 106 39 33 30 1.5 523 347 195 97 39 13 31 1.7 643 442 294 153 50 13 32 1.7 546 355 218 114 41 13 *= not within the scope of the invention
(126) The comparative examples clearly demonstrate that copolymer examples of the present invention having a monomer (C) of formula (I) with R.sub.2 derived from C.sub.10-C.sub.15-alcohols with a mean degree of branching (iso-index) in the range from 1.5-3.5 exhibit better thickening efficiency at high shear rates (10000 s.sup.−1) and a Newtonian rheology profile of the coating formulations.