US2007293634A1PendingUtilityA1
Method for the production of hyperbranched water-soluble polyesters
Est. expiryAug 30, 2022(expired)· nominal 20-yr term from priority
C08G 63/668C08G 83/005
56
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Claims
Abstract
Process for preparing essentially uncrosslinked hyperbranched, water-soluble or water-dispersible polyesters from dicarboxylic acids and polyether polyols having at least 3 OH groups. Water-soluble hyperbranched polyesters which are obtainable by such a process and their use for producing printing inks, adhesives, coatings, paints and varnishes.
Claims
exact text as granted — not AI-modified1 . A process for preparing essentially uncrosslinked hyperbranched, water-soluble or water-dispersible polyesters by reacting
at least one dicarboxylic acid or a dicarboxylic acid derivative (A) with at least one polyether polyol (B) having n OH groups, where n is ≧3, at from 40° C. to 160° C. in the presence of an esterification catalyst, where the components (A) and (B) are used in such amounts that the molar ratio of OH groups to COOH groups is from 2:1 to 1:2.
2 . A process as claimed in claim 1 , wherein n is 3, 4, 5 or 6.
3 . A process as claimed in claim 1 , wherein n is 3 or 4.
4 . A process as claimed in claim 1 , wherein the molar ratio of OH groups to COOH groups is from 1.8:1 to 1:1.8.
5 . A process as claimed in claim 1 , wherein the molar ratio of OH groups to COOH groups is from 1.5:1 to 1:1.5.
6 . A process as claimed in claim 1 , wherein the reaction is carried out under reduced pressure.
7 . A process as claimed in claim 6 , wherein the pressure is less than 500 mbar.
8 . A process as claimed in claim 1 , wherein the polyether polyol having at least 30H groups is obtainable by ethoxylation and/or propoxylation of a molecule having at least 3 acidic H atoms.
9 . A process as claimed in claim 8 , wherein an ethoxylation is carried out.
10 . A process as claimed in claim 1 , wherein a diol is additionally used as chain extender (V) in an amount of not more than 40 mol % based on the amount of polyether polyols used.
11 . A process as claimed in claim 10 , wherein the amount of the chain extender (V) is not more than 20 mol %.
12 . A process as claimed in claim 1 , wherein a monofunctional carboxylic acid or a monofunctional alcohol is additionally used as chain stopper (S) in an amount of not more than 10 mol % based on the amount of polyether polyols (B) or dicarboxylic acids (A) used.
13 . A process as claimed in claim 12 , wherein the amount of the chain stopper (S) is not more than 5 mol %.
14 . A process as claimed in claim 1 , wherein the hyperbranched, water-soluble or water-dispersible polyester obtained is reacted in an additional process step with a suitable functionalization reagent (F) which can react with the OH and/or COOH end groups of the polyester.
15 . A process as claimed in claim 14 , wherein the functionalization reagent (F) comprises one or more compounds selected from the group consisting of aliphatic and aromatic monocarboxylic acids and their derivatives, aliphatic and aromatic unsaturated monocarboxylic acids and their derivatives, aliphatic and aromatic monoalcohols, aliphatic and aromatic unsaturated monoalcohols, aliphatic and aromatic monoamines, aliphatic and aromatic unsaturated monoamines, aromatic and aliphatic monoisocyanates, aliphatic and aromatic unsaturated monoisocyanates, compounds containing carbodiimide groups and compounds containing epoxide groups.
16 . A process as claimed in claim 1 , wherein the esterification catalyst is an enzyme and the polymerization is carried out at from 40° C. to 120° C. in the presence of a solvent.
17 . A process as claimed in claim 16 , wherein the polymerization is carried out at from 50° C. to 80° C.
18 . A process as claimed in claim 16 , wherein the enzyme is a lipase or an esterase.
19 . A process as claimed in claim 18 , wherein the enzyme is Candida antarctica lipase B.
20 . A process as claimed in claim 16 , wherein the enzyme is used in immobilized form.
21 . A process as claimed in claim 1 , wherein the esterification catalyst is an acidic inorganic, organometallic or organic catalyst.
22 . A process as claimed in claim 21 , wherein the reaction is carried out at from 60° C. to 160° C.
23 . A process as claimed in claim 22 , wherein the reaction is carried out at from 80° C. to 150° C.
24 . A process as claimed in claim 21 , wherein the reaction is carried out at a pressure of not more than 100 mbar.
25 . A water-soluble or water-dispersible, hyperbranched polyester obtainable by a process as claimed in claim 1 .
26 . A water-soluble or water-dispersible, hyperbranched polyester which has a hydroxyl number of 50-1000 mg KOH/g, an acid number of 0-200 mg KOH/g, a number average molecular weight M n of 300-15 000 g/mol and a polydispersity M w /M n of 1.1-50 and is obtainable by a process as claimed in claim 1 .
27 . A water-soluble or water-dispersible, hyperbranched polyester as claimed in claim 26 which has a hydroxyl number of 100-800 mg KOH/g, an acid number of 1-100 mg KOH/g, a number average molecular weight M n of 500-8000 g/mol and a polydispersity M w /M n of 1.2-20.
28 . The use of a water-soluble or water-dispersible hyperbranched polyester as claimed in claim 25 for preparing polyaddition or polycondensation polymers.
29 . The use of a water-soluble or water-dispersible hyperbranched polyester as claimed in claim 25 for producing printing inks, adhesives, coatings, paints and varnishes.Join the waitlist — get patent alerts
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