Method for producing organyloxysilane-terminated polymers

Patent metadata

Field	Value
Publication number	US-12351683-B2
Application number	US-201917778863-A
Country	US
Kind code	B2
Filing date	Dec 13, 2019
Priority date	Dec 13, 2019
Publication date	Jul 8, 2025
Grant date	Jul 8, 2025

Abstract

A process for preparing silane-terminated polymers (SP) of the formula (I),

Y—[O—C(═O)—NH—(CR 1 2 ) b —SiR a (OR 2 ) 3-a ] x   (I),

includes in a 1 st process step at least one polymer (OHP) of the formula (II),

Y—[OH] x   (II),

being reacted with at least one isocyanate-functional silane (IS) of the formula (III),

O═C═N—(CR 1 2 ) b —SiR a (OR 2 ) 3-a   (III),

with the proviso that the isocyanate-functional silanes (IS) are used in an amount such that there are at least 1.05 isocyanate groups in the silanes (IS) to each hydroxyl group in the compounds (OHP). Subsequently, in a 2 nd process step, the unreacted isocyanate groups of the silanes (IS) are reacted, in the reaction mixture obtained in the 1 st process step, with at least one alcohol (A) of the formula (IV),

R 3 OH  (IV)

Subsequently, in a 3 rd process step, the reaction mixture obtained in the 2 nd process step is passed through an evaporation unit (VD).

First claim

The invention claimed is:

1. A process for preparing silane-terminated polymers (SP) of the formula (I)
Y—[O—C(—O)—NH—(CR 1 2 ) b —SiR a (OR 2 ) 3-a ]x  (I),

characterized in that
in a 1 st process step at least one polymer (OHP) of the formula (II)
Y—[OH] x   (II)

is reacted with at least one isocyanate-functional silane (IS) of the formula (III)
O═C═N—(CR 1 2 ) b —SiR a (OR 2 ) 3-a   (III)

with the proviso that the at least one isocyanate-functional silane (IS) is used in an amount such that there are at least 1.05 isocyanate groups in the at least one isocyanate-functional silane (IS) to each hydroxyl group in the at least one polymer (OHP),
where
Y is an x-valent polymer radical,
R may be identical or different and is a monovalent, optionally substituted hydrocarbon radical,
R 1 may be identical or different and is hydrogen atom or a monovalent, optionally substituted hydrocarbon radical,
R 2 may be identical or different and is hydrogen atom or a monovalent, optionally substituted hydrocarbon radical,
x is an integer from 1 to 50,
a may be identical or different and is 0, 1 or 2, and
b may be identical or different and is an integer from 1 to 10,
subsequently in a 2 nd process step the unreacted isocyanate groups of the silanes (IS)” with “unreacted isocyanate groups of the at least one isocyanate-functional silane (IS) are reacted, in the reaction mixture obtained in the 1 st process step, with at least one alcohol (A) of the formula (IV)
R 3 OH   (IV),

where
R 3 is a hydrocarbon radical having 1 to 4 carbon atoms, and a carbamatosilane (CS) is formed,
and subsequently in a 3 rd process step the reaction mixture obtained in the 2 nd process step is passed through an evaporation unit (VD) in which the reaction mixture in a layer thickness of not more than 5 cm is exposed to a pressure of at most 80 mbar and temperatures of at most 200° C., wherein the carbamatosilane (CS) formed in the 2 nd process step, of the formula (V)
R 30 —C(═O)—NH—(CR 1 2 ) b -SiR a (OR 2 ) 3-a   (V),

in which all the variables have the definition stated above, is at least partly evaporated and removed.

2. The process as claimed in claim 1 , wherein the carbamatosilane content in the reaction mixture obtained after the process of the invention is at most 0.3 wt %, based on the total weight of the reaction mixture.

3. The process as claimed in claim 1 , wherein the carbamatosilane content in the reaction mixture obtained after the process of the invention is at most 0.1 wt %, based on the total weight of the reaction mixture.

4. The process as claimed in claim 1 , wherein the isocyanatosilane (IS) is used in the 1 st process step in an amount such that there are at least 1.10 isocyanate groups in the compounds (IS) for each hydroxyl group of the polymer (OHP).

5. The process as claimed in claim 1 , wherein the 1 st and 2 nd process steps are carried out in the presence of a catalyst (K).

6. The process as claimed in claim 1 , wherein the 3 rd process step is carried out such that the reaction mixture has a mean residence time in the evaporation unit (VD) of at most 20 minutes.

7. The process as claimed in claim 1 , wherein the reaction mixture during the 3rd process step in the evaporator unit (VD) is exposed to a temperature of at most 180° C.

8. The process as claimed in claim 1 , wherein all the process steps are carried out under inert gas atmosphere.

Assignees

• Wacker Chemie Ag

Inventors

• Stanjek Volker
• Zander Lars

Classifications

• C08G2650/04

  End-capping · CPC title

• C08G18/718 Primary

  containing silicon · CPC title

• C08G65/336 Primary

  containing silicon · CPC title

• C08G18/48

  Polyethers · CPC title