Process for preparing a macromonomer

Patent metadata

Field	Value
Publication number	US-9657137-B2
Application number	US-201314652244-A
Country	US
Kind code	B2
Filing date	Dec 13, 2013
Priority date	Dec 17, 2012
Publication date	May 23, 2017
Grant date	May 23, 2017

Abstract

The present invention relates to a process for preparing hydrophobically associating macromonomers M and to the novel macromonomers prepared by means of the process according to the invention. The macromonomers M comprise a copolymerizable, ethylenically unsaturated group and a polyether structure in block form, the latter consisting of a polyethyleneoxy block and a hydrophobic polyalkyleneoxy block consisting of alkyleneoxy units having at least 4 carbon atoms. Optionally, the macromonomers M may have a terminal polyethyleneoxy block. The macromonomers prepared by the process according to the invention are suitable for reaction with further monomers, especially with acrylamide, to give a water-soluble, hydrophobically associating copolymer.

First claim

The invention claimed is:

1. A process for preparing a macromonomer M of the general formula (I)
H 2 C═C(R 1 )—R 2 —O—(—CH 2 —CH 2 —O—) k —(—CH 2 —CH(R 3 )—O—) l —(—CH 2 —CH 2 —O—) m —R 4   (I)

where the (—CH 2 —CH 2 —O—) k and (—CH 2 —CH(R 3 )—O—) l and optionally —(—CH 2 —CH 2 —O—) m units are arranged in block structure in the sequence shown in formula (I);
where the radicals and indices are each defined as follows:
k: is a number from 10 to 150;
l: is a number from 5 to 25;
m: is a number from 0 to 15;
R 1 : is H or methyl;
R 2 : is independently a single bond or a divalent linking group selected from the group consisting of —(C n H 2n )— and —O—(C n′ H 2n′ )—, where n is a natural number from 1 to 6 and n′ is a natural number from 2 to 6;
R 3 : is independently a hydrocarbyl radical having at least 2 carbon atoms or an ether group of the general formula —CH 2 —O—R 3′ where R 3′ is a hydrocarbyl radical having at least 2 carbon atoms; with the proviso that the sum total of carbon atoms in all hydrocarbyl radicals R 3 or R 3′ is in the range from 25.5 to 34.5;
R 4 is independently H or a hydrocarbyl radical having 1 to 4 carbon atoms;

comprising the steps of
a) reacting a monoethylenically unsaturated alcohol A1 of the general formula (II)
H 2 C═C(R 1 )—R 2 —OH  (II)

with ethylene oxide, where the R 1 and R 2 radicals are each as defined above;
with addition of an alkaline catalyst C1 comprising KOMe and/or NaOMe to obtain an alkoxylated alcohol A2;

b) reacting the alkoxylated alcohol A2 with at least one alkylene oxide Z of the formula (Z)

where R 3 is as defined above;
with addition of an alkaline catalyst C2;
where the concentration of potassium ions in the reaction in step b) is in the range from 0.01 to 0.5 mol %, based on the alcohol A2 used;
and where the reaction in step b) is performed at a temperature less than or equal to 135° C.,
to obtain an alkoxylated alcohol A3 of the formula (III)
H 2 C═C(R 1 )—R 2 —O—(—CH 2 —CH 2 —O—) k —(—CH 2 —CH(R 3 )—O—) l —R 4   (III)

where R 4 ═H, where the R 1 , R 2 and R 3 radicals and the indices k and 1 are each as defined above;

c) optionally reacting at least a portion of the alkoxylated alcohol A3 with ethylene oxide to obtain an alkoxylated alcohol A4 corresponding to the macromonomer M of the formula (I) where R 4 ═H and m is greater than 0;
d) optionally etherifying the alkoxylated alcohol A3 and/or A4 with a compound
R 4 —X

where R 4 is as defined above and X is a leaving group;
to obtain a macromonomer M of the formula (I) and/or (III) where R 4 =hydrocarbyl radical having 1 to 4 carbon atoms.

2. The process for preparing a macromonomer M according to claim 1 , wherein the alkaline catalyst C2 comprises at least one basic sodium compound.

3. The process for preparing a macromonomer M according to claim 1 , wherein a catalyst C2 comprising at least one basic sodium compound is used in step b), the concentration of sodium ions in the reaction in step b) being in the range from 3.5 to 12 mol %, based on the alcohol A2 used.

4. The process for preparing a macromonomer M according to claim 1 , wherein step b) is performed at temperatures of 120 to 135° C.

5. The process for preparing a macromonomer M according to claim 1 , wherein step b) comprises the addition of the at least one alkylene oxide Z to a mixture of alcohol A2 and alkaline catalyst C2 at a pressure in the range from 1 to 3.1 bar.

6. The process for preparing a macromonomer M according to claim 1 , wherein R 3 is a hydrocarbyl radical having 2 carbon atoms and step b) comprises the addition of the at least one alkylene oxide Z to a mixture of alcohol A2 and alkaline catalyst C2 at a pressure in the range from 1 to 3.1 bar, or R 3 is a hydrocarbyl radical having at least 3 carbon atoms and step b) comprises the addition of the at least one alkylene oxide Z to a mixture of alcohol A2 and alkaline catalyst C2 at a pressure in the range from 1 to 2.1 bar.

7. The process for preparing a macromonomer according to claim 1 , wherein k is a number from 23 to 26.

8. The process for preparing a macromonomer according to claim 1 , wherein the radicals and indices are each defined as follows:
k: is a number from 20 to 28;
l: is a number from 5 to 25;
m: is a number from 0 to 15;
R 1 : is H;
R 2 : is independently a divalent linking group —O—(C n′ H 2′ )— where n′ is a natural number from 3 to 5,
R 3 : is independently a hydrocarbyl radical having 2 to 4 carbon atoms, with the proviso that the sum total of the carbon atoms in all hydrocarbyl radicals R 3 or R 3′ is in the range from 25.5 to 34.5;
R 4 : is H.

9. The process for preparing a macromonomer according to claim 1 , wherein the radicals and indices are each defined as follows:
k: is a number from 23 to 26;
l: is a number from 5 to 25;
m: is a number from 0 to 15;
R 1 : is H;
R 2 : is independently a divalent linking group —O—(C n′ H 2n′ )— where n′ is a natural number from 3 to 5,
R 3 : is independently a hydrocarbyl radical having 2 to 4 carbon atoms, with the proviso that the sum total of the carbon atoms in all hydrocarbyl radicals R 3 or R 3′ is in the range from 25.5 to 34.5;
R 4 : is H.

10. The process for preparing a macromonomer according to claim 1 , wherein the radicals and indices are each defined as follows:
k: is a number from 23 to 26;
l: is a number from 7.5 to 25;
m: is a number from 0 to 15;
R 1 : is H;
R 2 : is independently a divalent linking group —O—(C n′ H 2n′ )— where n′ is a natural number from 3 to 5,
R 3 : is ethyl;
R 4 : is H.

11. The process for preparing a macromonomer according to claim 1 , wherein the radicals and indices are each defined as follows:
k: is a number from 23 to 26;
l: is a number from 8.5 to 11.5;
m: is a number from 0 to 15;
R 1 : is H;
R 2 : is independently a divalent linking group —O—(C n′ H 2n′ )— where n′ is a natural number from 3 to 5,
R 3 : is n-propyl;
R 4 : is H.

12. The process for preparing a macromonomer according to claim 1 , wherein the macromonomer M is a mixture of a macromonomer M of the formula (I) where m=0 and a macromonomer M of the formula (I) where m=1 to 15.

13. The process for preparing a macromonomer according to claim 12 , wherein the weight ratio of the macromonomer of the formula (I) where m=0 and the macromonomer of the formula (I) where m=1 to 15 is in the range from 19:1 to 1:19.

14. A macromonomer M of the general formula (I)
H 2 C═C(R 1 )—R 2 —O—(—CH 2 —CH 2 —O—) k —(—CH 2 —CH(R 3 )—O—) l —(—CH 2 —CH 2 —O—) m —R 4   (I)

where the (—CH 2 —CH 2 —O—) k and (—CH 2 —CH(R 3 )—O—) l and optionally —(—CH 2 —CH 2 —O—) m units are arranged in block structure in the sequence shown in formula (I);
where the radicals and indices are each defined as follows:
k: is a number from 20 to 28;
l: is a number from 5 to 25;
m: is a number from 0 to 15;
R 1 : is H or methyl;
R 2 : is independently a single bond or a divalent linking group selected from the group consisting of —(C n H 2n )— and —O—(C n′ H 2n′ )—, where n is a natural number from 1 to 6 and n′ is a natural number from 2 to 6;
R 3 : is independently a hydrocarbyl radical having at least 2 carbon atoms, with the proviso that the sum total of the carbon atoms in all hydrocarbyl radicals R 3 is in the range from 25.5 to 34.5;
R 4 : is independently H or a hydrocarbyl radical having 1 to 4 carbon atoms;
obtained by the pr

Assignees

• Basf Se

Inventors

• Bittner Christian
• Langlotz Björn
• Wenzke Benjamin
• Spindler Christian
• Reichenbach-Klinke Roland
• Klumpe Markus
• Meier Nicole
• Annen Ulrich
• Ostrowski Thomas

Classifications

• C08G65/2648

  Alkali metals or compounds thereof · CPC title

• C08F290/062

  Polyethers · CPC title

• C08F216/1425

  Monomers containing side chains of polyether groups · CPC title

• C08G65/2696 Primary

  characterised by the process or apparatus used · CPC title

• C08G2650/36

  Pre-polymer · CPC title