Addition compounds useful as dispersing agents and dispersion stabilizers, process for producing them, their use and solids coated therewith

• US 4,942,213 A
• Filed: 11/30/1988
• Issued: 07/17/1990
• Est. Priority Date: 12/04/1987
• Status: Expired due to Term

• Current Assignee: BYK-Chemie GmbH (Susanne Klatten, MBA)
• Original Assignee: BYK-Chemie GmbH (Susanne Klatten, MBA)
• Inventors: Pritschins, Wolfgang, Haubennestel, Karl-Heinz
• Primary Examiner(s): Welsh, Maurice J.
• Assistant Examiner(s): Sergent, Rabon
• Application Number:
  US07/278,112
• Time in Patent Office: 594 Days
• Field of Search: 528/49, 528/28
• US Class Current: 528/28
• CPC Class Codes: C08G 18/2805 Compounds having only one group containing active hydrogen vinylpolymers having terminal groups containing active hydrogen C08G18/62
• CPC Class Codes: C08G 18/283 Compounds containing ether groups, e.g. oxyalkylated monohydroxy compounds
• CPC Class Codes: C08G 18/284 Compounds containing ester groups, e.g. oxyalkylated monocarboxylic acids
• CPC Class Codes: C08G 18/6245 Polymers having terminal groups containing active hydrogen
• CPC Class Codes: C09K 23/16 Amines or polyamines

Abstract

Addition compounds suitable for use as dispersing agents and obtainable by reacting polyisocyanates having an average functionality of 2.5 to 10 with monohydroxy compounds, with compounds of formula II

G-(E).sub.n                                                II

wherein E represents --OH, --NH₂ and/or --NHR (wherein R represents an alkyl group having 1 to 4 carbon atoms) and n represents 2 or 3 and G represents an aliphatic, cycloaliphatic and/or aromatic group, and with compounds of formula III

Z-Q                                                        III

wherein Q represents --OH, --NH₂, --NHR (wherein R represents an alkyl group having 1 to 4 carbon atoms) or --SH and Z denotes a group containing at least one nitrogen-containing, basic group. The invention also relates to processes for the preparation of these addition compounds, to their use and to pulverulent or fibrous solids which are to be incorporated into liquid systems and which have been coated with these dispersing agents.

Claims

1. An addition compound or salt thereof useful as a dispersing agent or dispersion stabilizer obtained by

(a) reacting a polyisocyanate having an average functionality of 2.5 to 10 with a monohydroxy compound of formula I

View Dependent Claims (2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 23, 24, 25, 26)

2. An addition compound or salt thereof according to claim 1, wherein said polyisocyanate is reacted in the presence of a solvent.

3. An addition compound or salt thereof according to claim 1, wherein said polyisocyanate is reacted in the presence of a reaction catalyst.

4. An addition compound or salt thereof according to claim 1, wherein from 15 to 45% of the isocyanate groups originally present in the polyisocyanate are reacted in stage (a).

5. An addition compound or salt thereof according to claim 1, wherein from 20 to 40% of the isocyanate groups originally present in the polyisocyanate are reacted in stage (a).

6. An addition compound or salt thereof according to claim 1, wherein a further 5 to 45% of the isocyanate groups originally present in the polyisocyanate are reacted in stage (b) and a total of 30 to 65% of the isocyanate groups originally present in the polyisocyanate are reacted in stages (a) and (b).

7. An addition compound or salt thereof according to claim 1, wherein a further 15 to 40% of the isocyanate groups originally present in the polyisocyanate are reacted in stage (b) and a total of 40 to 60% of the isocyanate groups originally present in the polyisocyanate are reacted in stages (a) and (b).

8. An addition compound or salt thereof according to claim 1, wherein said vinyl comonomer is selected from the group consisting of vinyl esters, vinyl ethers, styrene, vinyltoluene and vinylcyclohexane.

9. An addition compound or salt thereof according to claim 1, wherein at least 5 mole % of the compound of formula I defined above is replaced by a compound of formula Ia or by a monohydroxyfunctional polyacrylic or polymethacrylic acid ester or a copolymer thereof, or at least 5 mole % of the compound of formula II defined above is replaced by a compound of formula IIa.

10. An addition compound or salt thereof according to claim 1, wherein at least 50 mole % of the compound of formula I defined above is replaced by a compound of formula Ia or by a monohydroxyfunctional polyacrylic or polymethacrylic acid ester or a copolymer thereof, or at least 50 mole % of the compound of formula II defined above is replaced by a compound of formula IIa.

11. An addition compound or salt thereof according to claim 1, wherein said monohydroxy compound of formula Ia is selected from the group consisting of polyurethanes, polyether-polyurethanes, polyester-polyurethanes and polyether-polyester-polyurethanes having average molecular weights M_n of 500 to 3000.

12. An addition compound or salt thereof according to claim 1, wherein said compound of formula IIa is selected from the group consisting of polyurethanes, polyether-polyurethanes, polyester-polyurethanes and polyether-polyester-polyurethanes having 2 to 3 OH groups and average molecular weights M_n of 300 to 2500.

23. A process of stabilizing a dispersion of a pulverulent or fibrous solid in a liquid system comprising the step of adding to said system an effective dispersion stabilizing amount of an addition compound or salt thereof according to claim 1.

24. A process according to claim 23, wherein said solid is a pigment particle.

25. A process of increasing the dispersibility of a pulverulent or fibrous solid in a liquid system comprising the step of applying to said solid an effective dispersibility enhancing amount of an addition compound or salt thereof according to claim 1.

26. A process according to claim 25, wherein said solid is a pigment particle.

13. A process for producing an addition compound or salt thereof useful as a dispersing agent or dispersion stabilizer comprising the steps of:

(a) reacting a polyisocyanate having an average functionality of 2.5 to 10 with a monohydroxy compound of formula I

space="preserve" listing-type="equation">Y--OH I

in which Y represents

(i) an aliphatic or cycloaliphatic hydrocarbon group having 8 to 30 carbon atoms in which hydrogen atoms may be partly replaced by halogen or aryl substituents, or

(ii) an aliphatic, cycloaliphatic or aromatic group containing at least one --O-- or --COO-- group, having an average molecular weight M_n of 200 to 10,000, and in which hydrogen atoms may be partly replaced by halogen,

in an amount sufficient to react 10 to 70% of the isocyanate groups originally present in the isocyanate;

(b) reacting with a compound of formula II

space="preserve" listing-type="equation">G--(E).sub.n II

in which

E represents at least one of --OH, --NH₂ and --NHR in which R is an alkyl group having 1 to 4 carbon atoms,

n represents 2 or 3, and

G represents an aliphatic, cycloaliphatic and/or aromatic group containing at least 2 carbon atoms, having an average molecular weight M_n of not more than 3000, and which may contain at least one group selected from the group consisting of --O--, --COO--, --CONH--, --S-- and --SO₂ --,

in an amount sufficient to react 1 to 50% of the isocyanate groups originally present in the isocyanate, and to react a total of 20 to 85% of the isocyanate groups originally present in the polyisocyanate in stages (a) and (b); and

(c) reacting with a compound of formula III

space="preserve" listing-type="equation">Z--(CH.sub.2).sub.p --Q III

in which

Q represents --OH, --SH, --NH₂ or --NHR in which R is an alkyl group having 1 to 4 carbon atoms,

Z represents an aliphatic group having 2 to 10 C atoms and carrying at least one tertiary amino group or represents a heterocyclic group having at least one basic ring nitrogen atom not bonded to a hydrogen atom, and

p is 0 when Z is an aliphatic group or an integer from 0 to 10 when Z is a heterocyclic group,

in an amount sufficient to provide at least one molecule of formula III for each isocyanate group in the polyisocyanate unreacted after stages (a) and (b);

wherein

at least 1 mole % of the compound of formula I defined above is replaced by a compound of formula Ia

space="preserve" listing-type="equation">Y'"'"'--OH Ia

in which Y'"'"' represents an aliphatic, cycloaliphatic or aromatic group having an average molecular weight M_n of 200 to 10,000 in which hydrogen atoms may be partly replaced by halogen and containing at least one --NHCOO-- group, or

at least 1 mole % of the compound of formula I defined above is replaced by a monohydroxyfunctional polyacrylic or polymethacrylic acid ester or a copolymer thereof with up to 50 mole % relative to monomer units of a vinyl comonomer, having an average molecular weight M_n of not more than 10,000, or

at least 1 mole % of the compound of formula II defined above is replaced by a compound of formula IIa

space="preserve" listing-type="equation">G'"'"'--(OH).sub.n IIa

in which G'"'"' represents an aliphatic, cycloaliphatic or aromatic group containing at least 2 carbon atoms, having an average molecular weight M_n of not more than 3000, and containing at least one --NHCOO-- or --Si(CH₃)₂ O-- group, and n represents a number from 2 to 3.

14. A process according to claim 13, wherein the reaction product of stage (c) is an addition compound incorporating at least one basic nitrogen group, further comprising the step of reacting the product of stage (c) with an acid to form an acid addition salt.

15. A process according to claim 13, wherein from 15 to 45% of the isocyanate groups originally present in the polyisocyanate are reacted in stage (a).

16. A process according to claim 13, wherein from 20 to 40% of the isocyanate groups originally present in the polyisocyanate are reacted in stage (a).

17. A process according to claim 13, wherein a further 5 to 45% of the isocyanate groups originally present in the polyisocyanate are reacted in stage (b) and a total of 30 to 65% of the isocyanate groups originally present in the polyisocyanate are reacted in stages (a) and (b).

18. A process according to claim 13, wherein a further 15 to 40% of the isocyanate groups originally present in the polyisocyanate are reacted in stage (b) and a total of 40 to 60% of the isocyanate groups originally present in the polyisocyanate are reacted in stages (a) and (b).

19. A process according to claim 13, wherein at least 5 mole % of the compound of formula I defined above is replaced by a compound of formula Ia or by a monohydroxyfunctional polyacrylic or polymethacrylic acid ester or a copolymer thereof, or at least 5 mole % of the compound of formula II defined above is replaced by a compound of formula IIa.

20. A process according to claim 13, wherein at least 50 mole % of the compound of formula I defined above is replaced by a compound of formula Ia or by a monohydroxyfunctional polyacrylic or polymethacrylic acid ester or a copolymer thereof, or at least 50 mole % of the compound of formula II defined above is replaced by a compound of formula IIa.

21. A process according to claim 13, wherein the monohydroxy compound of formula Ia is selected from the group consisting of polyurethanes, polyether-polyurethanes, polyester-polyurethanes and polyether-polyester-polyurethanes having average molecular weights M_n of 500 to 3000.

22. A process according to claim 13, wherein the compound of formula IIa is selected from the group consisting of polyurethanes, polyether-polyurethanes, polyester-polyurethanes and polyether-polyester-polyurethanes having 2 to 3 OH groups and average molecular weights M_n of 300 to 2500.

27. Liquid dispersible pulverulent or fibrous solids coated with a dispersing agent comprising an addition compound or salt thereof obtained by

(a) reacting a polyisocyanate having an average functionality of 2.5 to 10 with a monohydroxy compound of formula I

View Dependent Claims (28)

28. Pulverulent solids according to claim 27, wherein said solids are pigment particles.