Polymeric tertiary and secondary amines with a silica-type backbone, processes for their preparation, and use

Claim 2

A polymeric tertiary or secondary organosiloxane amine with a silica-type backbone, comprised of units of the formula: ##STR22## in which R 1 and R 2 represent a group of the formula ##STR23## R 4 is alkylene having 3 to 10 C atoms or cycloalkylene having 5 to 8 C atoms or represents the units ##STR24## in which n indicates 1 to 6 methylene, R 1 and R 2 can be identical or different and the free valencies of the oxygen atoms are saturated either by silicon atoms of further groups of the formula (2) and/or by crosslinking bridge members ##STR25## in which R' is methyl or ethyl and in which the ratio of the silicon atoms in (2) to the bridge atoms silicon, titanium and aluminum is 1:0 to 1:10, R 3 has the same general meaning as R 1 and R 2 or represents hydrogen, a linear or branched alkyl having 1 to 10 C atoms or cycloalkyl having 5 to 8 C atoms or benzyl.

Claim 3

A polymeric tertiary or secondary organosiloxane amine as claimed in claim 1, wherein R 4 is linear or branched alkylene.

Claim 4

A polymeric tertiary or secondary organosiloxane amine as claimed in claim 1 or 2, wherein R 1 , R 2 and R 3 are identical to one another.

Claim 5

A polymeric amine as claimed in claims 1 or 2, comprised of units N(CH.sub.2 --CH.sub.2 --CH.sub.2 SiO.sub.3/2).sub.3

Claim 6

A process for preparing the polymeric tertiary organosiloxane amine as claimed in claims 1 or 2, comprising reacting a primary amine having a substituent comprised of: an alkyl group having 1 to 10 C atoms, a cycloalkyl group having 5 to 8 C atoms, a benzyl group, an alkylene group having 3 to 10 C atoms or a cycloalkylene grouping having 5 to 8 C atoms, said alkylene group being bonded to a trialkoxysilyl group wherein the alkoxy contains 1 to 5 C atoms, or of a group ##STR26## in which n indicates 1 to 6 methylene groups, with a halogenoorganotrialkoxysilane wherein the alkoxy contains 1 to 5 C atoms and in which the organic group is alkylene having 3 to 10 C atoms, cycloalkylene having 5 to 8 C atoms or ##STR27## in which n indicates 1 to 6 halogen-terminated methylene, in the course of 5 to 48 hours to form a quanternary salt, deprotonating the resulting quaternary salts by means of at least stoichiometric amounts of an organic or inorganic base, distilling to recover the amine components formed and reacting the component which predominantly contains tertiary amine with at least the amount of water required for complete hydrolysis and condensation and drying.

Claim 7

The process as defined in claim 5, which further comprises heat-treating at about 200°-350° C.

Claim 8

A process for preparing the polymeric tertiary organosiloxane amine as claimed in claims 1 or 2 comprising reacting a secondary bis-(trialkoxysilylorgano)amine in which the organic group has the meaning of R 4 and the alkoxy groups have 1 to 5 C atoms with a halogenoorganotrialkoxysilane in which organic group and alkoxy groups have the same meaning as in the said secondary bis-(trialkoxysilylorgano)amine reactant, or with a linear or branched alkyl halide having 1 to 10 C atoms, a cycloalkyl halide having 5 to 8 C atoms or a benzyl halide, deprotonating the resulting quaternary salt with at least stoichiometric amounts of an organic or inorganic base, and further reacting the tertiary amine with at least the amount of water required for complete hydrolysis and condensation, and drying.

Claim 9

A process for preparing the polymeric tertiary organosiloxane amine as claimed in claim 1 or 2, comprising reacting a secondary amine having a trialkoxysilylorgano substituent in which the organic group has the meaning of R 4 and the alkoxy groups have 1 to 5 C atoms and a substituent comprised of a linear or branched alkyl group having 1 to 10 C atoms or a cycloalkyl group having 5 to 8 C atoms or a benzyl group with a halogenoorganotrialkoxysilane in which organic group and alkoxy groups have the same meaning as in the case of the trialkoxysilylorgano substituents of the said secondary amine reactant, deprotonating the resulting quaternary salt, with at least stoichiometric amounts of an organic or inorganic base, and further reacting the tertiary amine, with at least the amount of water required for complete hydrolysis and condensation, and drying.

Claim 10

The process as claimed in claim 5, wherein the primary amine is reacted with an iodo-, bromo- or chloro-organotrialkoxysilane.

Claim 11

The process as claimed in claim 7, wherein the secondary amine is reacted with an iodo-, bromo- or chloro-organotrialkoxysilane.

Claim 12

The process as claimed in claim 8, wherein the secondary amine is reacted with an iodo-, bromo- or chloro-organotrialkoxysilane.

Claim 13

The process as claimed in claim 5, wherein the alkyl group and/or trialkoxysilylalkyl group on the amine nitrogen and the alkyl group in the halogenoalkyltrialkoxysilane are linear or branched.

Claim 14

The process as claimed in claim 5, wherein the reaction of the amine with the halogenoorganotrialkoxysilane is carried out at a temperature between room temperature and 300° C.

Claim 15

The process as claimed in claim 13, wherein the reaction is carried out at an elevated pressure which corresponds to the sum of the partial pressures of the components of the reaction mixture at the reaction temperature used.

Claim 16

The process as claimed in claim 5, wherein sodium methylate, potassium methylate, sodium ethylate, potassium ethylate, sodium propylate, potassium propylate, sodium butylate, potassium butylate, sodium pentylate, potassium pentylate, alkali metal hydroxide, alkaline earth metal hydroxide, alkali metal bicarbonate, alkali metal carbonate or ammonia are used for the deprotonation.

Claim 17

The process as claimed in claim 15, wherein the deprotonation is carried out in an organic solvent.

Claim 18

The process as claimed in claim 5, wherein the hydrolysis and condensation are carried out at room temperature to reflux temperature of the reaction mixture.

Claim 19

The process as claimed in claim 5, wherein drying is carried out at room temperature to 250° C., if desired in vacuo.

Claim 20

The process as claimed in claim 6, wherein the heat treating is carried out for at least one hour up to four days.

Claim 21

A process for preparing the secondary polymeric amine as claimed in claim 1 or 2, comprising reacting a bis-(trialkoxysilanorgano)-amine in which the organic group has the meaning of R 4 and the alkoxy groups have 1 to 5 C atoms, with at least the amount of water required for complete hydrolysis and condensation and drying.

Claim 22

The process of claim 20, wherein the dried solid is heated at about 200°-350° C.

Claim 23

The process as claimed in claim 20, wherein the trialkoxysilylalkyl groups on the amine nitrogen are linear or branched.

Claim 24

The process as claimed in claim 20, wherein the hydrolysis and condensation are caried out at room temperature to the reflux temperature of the reaction mixture.

Claim 25

The process as claimed in claim 20, wherein drying is carried out at room temperature to 250° C., if desired in vacuo.

Claim 26

The process as claimed in claim 20, wherein a heat treatment is carried out for at least one hour up to four days.

Claim 27

A process for preparing the polymeric tertiary organosiloxane amine as claimed in claim 1 or 2, wherein R 1 , R 2 and R 3 are identical comprising reacting ammonia with a halogenoorganotrialkoxysilane in which the organic group is alkylene having 3 to 10 carbons, or cycloalkylene of 5 to 8 carbons, or ##STR28## wherein n is 1 to 6, and the alkoxy groups have 1 to 5 C atoms, at a temperature from below room temperature to 250° C. and under a pressure which corresponds to the sum of the partial pressures of the components of the reaction mixture at the reaction temperature used, 1-20 moles of ammonia being employed per 1 mole of halogenoorganotrialkoxysilane, substantially removing excess ammonia, separating off the resulting inorganic salt, removing by distillation ammonia residues as well as small amounts of primary and secondary amines which have been formed and further reacting the remaining tertiary amine, with at least the amount of water required for complete hydrolysis and condensation and drying.

Claim 28

The process as claimed in claim 26, wherein ammonia is reacted with an iodo-, bromo- or chloro-organotrialkoxysilane.

Claim 29

The process as claimed in claim 26, wherein the alkyl in the halogenoalkyltrialkoxysilane is linear or branched.

Claim 30

The process of claim 5 which further comprises reacting the primary amine with the said silane in the presence of a solubilizer.

Claim 31

The process of claim 29 which further comprises deprotonating in a solubilizer.

Claim 32

The process of claim 30 which further comprises, after deprotonating, separating an inorganic salt from the liquid phase.

Claim 33

The process of claim 5 which further comprises reacting said amine component with water after adding at least one of a solubilizer or crosslinking agent of the general formula: Me(OR).sub.2-4 R'.sub.0-2 or Al(OR).sub.2-3 R'.sub.0-1 which Me is Si, or Ti, R is alkyl of 1 to 5 carbons, and R' is methyl or ethyl.

Claim 34

The process of claim 7 which further comprises deprotonating the quaternary salt in a solubilizer.

Claim 35

The process of claim 33 which further comprises separating the resulting inorganic salt from the liquid phase.

Claim 36

The process of claim 7 which further comprises reacting said tertiary amine with water after adding at least one of a solubilizer or a crosslinking agent of the formula: Me(OR).sub.2-4 R'.sub.0-2 or Al(OR).sub.2-3 R'.sub.0-1 wherein Me is Si or Ti, R is alkyl of 1 to 5 carbons and R' is methyl or ethyl.

Claim 37

The process of claim 7 wherein the product is heat treated at about 200°-350° C.

Claim 38

The process of claim 8 which further comprises deprotonating in the presence of a solubilizer.

Claim 39

The process of claim 8 which further comprises separating the resulting inorganic salt from the liquid phase after deprotonating.

Claim 40

The process of claim 8 which further comprises reacting said tertiary amine with water after adding at least one of a solubilizer or a crosslinking agent of the formula: Me(OR).sub.2-4 R'.sub.0-2 or Al(OR).sub.2-3 R'.sub.0-1 wherein Me is Si or Ti, R is alkyl of 1 to 5 carbons and R' is methyl or ethyl.

Claim 41

The process of claim 8 which further comprises heating the product at 200°-350° C.

Claim 42

The process of claim 16 wherein the solvent is an alcohol which corresponds to the alkoxyl groups bonded to the silicon atoms of one or both reactants.

Claim 43

The process of claim 20 which further comprises adding a solubilizer.

Claim 44

A process for preparing a polymeric tertiary organosiloxane amine comprised of units of the formula: N(CH.sub.2 CH.sub.2 CH.sub.2 SiO.sub.3/2).sub.3 comprising reacting ammonia with a halogenoorganotrialkoxysilane in which the organic group is alkylene having 3 carbons, and the alkoxy groups have 1 to 5 C atoms, at temperature from below room temperature to 250° C. and under a pressure which corresponds to the sum of the partial pressures of the components of the reaction mixture at the reaction temperature used, 1-20 moles of ammonia being employed per 1 mole of halogenoorganotrialkoxysilane, substantially removing excess ammonia, separating off the resulting inorganic salt, removing by distillation ammonia residues as well as small amounts of primary and secondary amines which have been formed and further heating the remaining tertiary amine, with at least the amount of water required for complete hydrolysis and condensation and drying.

Claim 45

A process for preparing a polymeric tertiary organosiloxane amine comprised of units of the formula: N(CH.sub.2 CH.sub.2 CH.sub.2 SiO.sub.3/2).sub.3 comprising reacting ammonia with a halogenoorganotrialkoxysilane in which the organic group is alkylene having 3 carbons, and the alkoxy groups have 1 to 5 C atoms, at temperature from below room temperature to 250° C. and under a pressure which corresponds to the sum of the partial pressures of the components of the reaction mixture at the reaction temperature used, 1-20 moles of ammonia being employed per 1 mole of halogenoorganotrialkoxysilane, substantially removing excess ammonia, separating off the resulting inorganic salt, removing by distillation ammonia residues as well as small amounts of primary and secondary amines which have been formed and further heating the remaining tertiary amine, with at least the amount of water required for complete hydrolysis and condensation and drying.

Claim 46

The process of claim 26 wherein the reaction of ammonia with said alkoxysilane takes place in the presence of a solubilizer.

Claim 47

The process of claim 26 which further comprises adding at least one of a solubilizer or crosslinking agent of the formula: Me(OR).sub.2-4 R'.sub.0-2 or Al(OR).sub.2-3 R'.sub.0-1 wherein Me is Si or Ti, R is alkyl containing 1 to 5 carbons, and R' is methyl or ethyl.

Claim 48

The process of claim 26 where the product is heated at 200°-350° C.

Claim 49

The process of claim 43 where the reaction of ammonia with said alkoxysilane takes place in the presence of a solubilizer.

Claim 50

The process of claim 43 which further comprises adding at least one of a solubilizer or crosslinking agent of the formula: Me(OR).sub.2-4 R'.sub.0-2 or Al(OR).sub.2-3 R'.sub.0-1 wherein Me is Si or Ti, R is alkyl containing 1 to 5 carbons, and R' is methyl or ethyl.

Claim 51

The process of claim 43 where the product is heated at 200°-350° C.