Control of sugar evaporator scale using sugar or sugar moieties
US-2015345032-A1 · Dec 3, 2015 · US
US10344249B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-10344249-B2 |
| Application number | US-201414902397-A |
| Country | US |
| Kind code | B2 |
| Filing date | Jul 2, 2014 |
| Priority date | Jul 3, 2013 |
| Publication date | Jul 9, 2019 |
| Grant date | Jul 9, 2019 |
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The present invention concerns a method for producing a gel-like polymer composition, in which an [alpha],[beta]-ethylenically unsaturated carboxylic acid is subject to radical polymerization in the presence of at least one polyether component, the gel-like polymer composition obtainable using this method and the use thereof.
Opening claim text (preview).
The invention claimed is: 1. A process for preparing a polymer composition in gel form, comprising a) providing a monomer composition M) comprising A) at least one α,β-ethylenically unsaturated carboxylic acid, and B) less than 0.1% by weight, based on the total weight of the monomer composition M), of crosslinking monomers having two or more polymerizable α,β-ethylenically unsaturated double bonds per molecule, where component A) is optionally partly replaced by C) at least one unsaturated sulfonic acid or unsaturated phosphonic acid, b) subjecting the monomer composition M) provided in step a) to a free-radical polymerization in the presence of at least one polyether component PE), which does not have any copolymerizable double bonds, selected from polyetherols having a number-average molecular weight of at least 200 g/mol and the mono- and di-(C 1 -C 6 -alkyl ethers) thereof, surfactants containing polyether groups and mixtures thereof, and wherein the free-radical polymerization in step b) is additionally effected in the presence of a solvent S) selected from the group consisting of water, C 1 -C 6 -alkanols, polyols other than PE), the mono- and dialkyl ethers thereof, aprotic polar solvents and mixtures thereof, to prepare a polymer in gel form. 2. The process according to claim 1 , wherein the polyether component PE) comprises a polyetherol having repeat propylene oxide units or a mono-or di-(C 1 -C 6 -alkyl ether) of a polyetherol having repeat propylene oxide units, and the proportion of these repeat propylene oxide units averages not more than 18 units per molecule. 3. The process according to claim 1 , wherein the polymer composition in gel form comprises at least 10% by weight, based on the total weight of the polymer composition, of at least one solvent S) selected from the group consisting of water, C 1 -C 6 -alkanols, polyols other than PE), the mono- and dialkyl ethers thereof, aprotic polar solvents and mixtures thereof. 4. The process according to claim 1 , wherein the polymerization in step b) is effected in feed mode, by initially charging at least a portion of the polyether component PE) and optionally, at least a portion of the solvent S), and supplying at least a portion of the monomer composition provided in step a) and at least one free-radical initiator FRI) to the initial charge. 5. The process according to claim 1 , wherein the free-radical polymerization in step b) is effected in the presence of the solvent S) and the reaction mixture at the start of the reaction in step b) comprises the solvent S) in an amount of 0% to 90% by weight, based on the total weight of the reaction mixture, the reaction mixture after conclusion of the reaction in step b) comprises the solvent S) in an amount of 0% to 50% by weight, based on the total weight of the reaction mixture. 6. The process according to claim 1 , wherein the solvent S) is selected from the group consisting of propylene glycol, dipropylene glycol, water, and mixtures thereof. 7. The process according to claim 1 , wherein the solvent S) comprises at least 50% by weight, based on the total weight of the solvent S), of water. 8. The process according to claim 1 , wherein the free-radical polymerization in step b) is effected in feed mode, and feeds comprising at least one α,β-ethylenically unsaturated carboxylic acid do not comprise any solvent S). 9. The process according to claim 1 , wherein the polymerization in step b) is effected at a temperature in the range from 20 to 90° C. 10. The process according to claim 1 , wherein the α,β-ethylenically unsaturated carboxylic acid A) is selected from the group consisting of acrylic acid, methacrylic acid, ethacrylic acid, α-chloroacrylic acid, crotonic acid, maleic acid, itaconic acid, citraconic acid, mesaconic acid, glutaconic acid, aconitic acid, fumaric acid, and mixtures thereof. 11. The process according to claim 1 , wherein the monomer composition M) further comprises, as component C), at least one unsaturated sulfonic acid or unsaturated phosphonic acid. 12. The process according to claim 1 , wherein the monomer composition M) comprises at least 50% by weight, based on the total weight of the monomer composition M), of acrylic acid. 13. The process according to claim 1 , wherein the monomer composition M) additionally comprises at least one monomer D) selected from the group consisting of compounds of the general formulae (I.a) and (I.b) wherein the sequence of the alkylene oxide units is arbitrary, k and l are each independently an integer from 0 to 1000, where the sum of k and 1 is at least 2, R 1 is hydrogen or C 1 -C 8 -alkyl, R 2 is hydrogen, C 1 -C 30 -alkyl, C 2 -C 30 -alkenyl or C 5 -C 8 -cycloalkyl, X is O or a group of the formula NR 3 in which R 3 is H, alkyl, alkenyl, cycloalkyl, heterocycloalkyl, aryl or hetaryl. 14. The process according to claim 1 , wherein the monomer composition M) additionally comprises at least one comonomer selected from the group consisting of E) vinylaromatics, F) C 2 -C 8 monoolefins, nonaromatic hydrocarbons having at least two conjugated double bonds, G) esters of α,β-ethylenically unsaturated mono- and dicarboxylic acids with C 1 -C 30 -alkanols, H) compounds having one free-radically polymerizable α,β-ethylenically unsaturated double bond and at least one cationogenic and/or cationic group per molecule, I) esters of vinyl alcohol or allyl alcohol with C 1 -C 30 -monocarboxylic acids, K) monomers containing amide groups, L) esters of α,β-ethylenically unsaturated mono- and dicarboxylic acids with C 2 -C 30 -alkanediols, amides of α,β-ethylenically unsaturated mono- and dicarboxylic acids with C 2 -C 30 -amino alcohols having a primary or secondary amino group, M) α,β-ethylenically unsaturated nitriles, N) vinyl halides, vinylidene halides, O) monomers having urea groups, and mixtures thereof. 15. The process according to claim 1 , wherein the monomer composition M) comprises acrylic acid and at least one comonomer selected from the group consisting of α,β-ethylenically unsaturated carboxylic acids other than acrylic acid and derivatives thereof, C 2 -C 10 -monoolefins, nonaromatic hydrocarbons having at least two conjugated double bonds, vinylaromatics, N-vinyllactams and mixtures thereof. 16. The process according to claim 1 , wherein the monomer composition M) consists of acrylic acid. 17. The process according to claim 1 , wherein the polyether component PE) comprises at least one polyetherol having a number-average molecular weight in the range from about 200 to 100 000 g/mol or a mono- or di-(C 1 -C 2 -alkyl ether) thereof. 18. The process according to claim 1 , wherein the polyether component PE) comprises at least one polyetherol or a mono- or di-(C 1 -C 2 -alkyl ether) thereof comprising exclusively ethylene oxide units as alkylene oxide units. 19. The process according to claim 1 , wherein the polyether component PE) comprises at least one surfactant containing polyether groups, selected from the group consisting of alkyl polyoxyalkylene ethers, aryl polyoxyalkylene ethers, alkylaryl polyoxyalkylene ethers, alkoxylated animal and/or vegetable fats and/or oils, fatty amine alkoxylates, fatty acid amide alkoxylates, fatty acid diethanolamide alkoxylates, polyoxyethylene sorbitan fatty acid esters, alkyl polyether sulfates, aryl polyether sulfates, alkylaryl polyether sulfates, alky
Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds, e.g. carbomers {, poly(meth)acrylates, or polyvinyl pyrrolidone} · CPC title
Homopolymers or copolymers of acids; Metal or ammonium salts thereof · CPC title
(Co)polymerised carboxylic acids, -anhydrides, -esters in solid and liquid compositions · CPC title
Polymerisation in the presence of compounding ingredients, e.g. plasticisers, dyestuffs, fillers · CPC title
Polyalkylene oxides · CPC title
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