Production of noncyclic polyalkylene polyamines

Claim 2

A process for preparing predominantly noncyclic polyalkylene polyamines which comprises: contacting ammonia or a primary or secondary amine with an alkanolamine compound having an amino group and a primary or secondary hydroxy group and an alkyleneamine compound having two amino groups in the presence of a catalytically effective amount of a Group IIIB metal acid phosphate at a temperature sufficient to effect a reaction among the ammonia or amine, the alkanolamine compound and the alkyleneamine compound under a pressure sufficient to maintain a substantial amount of the ammonia or amine in the reaction zone.

Claim 3

The process of claim 1 in which the Group IIIB metal is scandium, yttrium, lanthanum or a rare earth lanthanide having an atomic number from 58 to 71.

Claim 4

The process of claim 1 in which the catalyst is a Group IIIB metal monohydrogen phosphate.

Claim 5

The process of claim 3 in which the catalyst is a monohydrogen phosphate salt of lanthanum, yttrium, neodymium, cerium, praseodymium or samarium.

Claim 6

The process of claim 1 in which the catalyst is a Group IIIB dihydrogen phosphate.

Claim 7

The process of claim 5 in which the catalyst is a dihydrogen phosphate salt of lanthanum, praseodymium, neodymium, samarium, dysprosium or gadolinium.

Claim 8

The process of claim 1 in which the temperature is from about 175° C. to 400° C. and the pressure is at least 1 atmosphere.

Claim 9

The process of claim 7 in which the catalyst is a lanthanum acid phosphate.

Claim 10

The process of claim 1 in which the molar ratio of alkyleneamine to alkanolamine is from 0.5:1 to 12:1.

Claim 11

The process of claim 1 in which the molar ratio of ammonia or amine to total alkyleneamine compound and alkanolamine compound is about 0.25:1 to 15:1.

Claim 12

A process for preparing a noncyclic polyalkylene polyamine which comprises: (a) contacting an alkanolamine compound having a primary amino group and a primary or secondary hydroxyl group of the general formula ##STR7## where R is hydrogen or a lower alkyl (C 1 -C 4 ) radical, x is a number from 2 to 6, and y is a number from 0 to 3, with ammonia and an alkyleneamine compound having two primary amino groups of the general formula: ##STR8## where R is hydrogen or a lower alkyl (C 1 -C 4 ) radical, x' is a number from 2 to 6, and y' is a number from 1 to 4, in the presence of a catalytically effective amount of an acid phosphate salt of a Group IIIB metal at a temperature from about 210° C. to about 350° C. under a pressure sufficient to maintain a substantial amount of the ammonia in the reaction zone, and (b) recovering the noncyclic polyalkylene polyamine from the resultant reaction mixture.

Claim 13

A process for preparing a noncyclic polyalkylene polyamine which comprises: (a) contacting an alkanolamine compound having a primary amino group and a primary or secondary hydroxyl group of the general formula ##STR7## where R is hydrogen or a lower alkyl (C 1 -C 4 ) radical, x is a number from 2 to 6, and y is a number from 0 to 3, with ammonia and an alkyleneamine compound having two primary amino groups of the general formula: ##STR8## where R is hydrogen or a lower alkyl (C 1 -C 4 ) radical, x' is a number from 2 to 6, and y' is a number from 1 to 4, in the presence of a catalytically effective amount of an acid phosphate salt of a Group IIIB metal at a temperature from about 210° C. to about 350° C. under a pressure sufficient to maintain a substantial amount of the ammonia in the reaction zone, and (b) recovering the noncyclic polyalkylene polyamine from the resultant reaction mixture.

Claim 14

The process of claim 11 in which the catalyst is an acid phosphate salt of a Group IIIB metal selected from the group consisting of scandium, yttrium, lanthanum and the rare earth lanthanides having an Atomic Number from 58 to 71.

Claim 15

The process of claim 12 in which the alkanolamine is an ethanolamine when R is hydrogen or a lower alkyl (C 1 -C 4 ) radical, x is 2 and y is 0 to 3, and the alkyleneamine is an ethyleneamine when R is hydrogen or a lower alkyl (C 1 -C 4 ) radical, x' is 2 and y' is 1 to 4.

Claim 16

The process of claim 13 in which the alkanolamine is monoethanolamine and the ethyleneamine is ethylenediamine.

Claim 17

The process of claim 14 in which the molar ratio of ethylenediamine:monoethanolamine:ammonia is from 0.75-10:0.5-2:0.35-20.

Claim 18

The process of claim 15 in which the catalyst is a Group IIIB metal monohydrogen phosphate.

Claim 19

The process of claim 16 in which the catalyst is a monohydrogen phosphate salt of lanthanum, neodymium or praseodymium.

Claim 20

The process of claim 15 in which the catalyst is a Group IIIB metal dihydrogen phosphate.

Claim 21

The process of claim 18 in which the catalyst is a dihydrogen phosphate salt of lanthanum, neodymium or praseodymium.

Claim 22

A process for preparing a noncyclic polyalkylene polyamine which comprises: (a) contacting an alkanolamine compound having an amino group and a primary or secondary hydroxy group of the general formula: ##STR9## where R is hydrogen or a lower alkyl (C 1 -C 4 ) radical, R' is hydrogen or an alkyl (C 1 -C 25 ) radical, x is a number from 2 to 6, and y is a number from 0 to 3 with an alkyleneamine compound having two amino groups of the general formula: ##STR10## where R is a hydrogen or a lower alkyl (C 1 -C 4 ) radical, R' is hydrogen or an alkyl (C 1 -C 25 ) radical, x' is a number from 2 to 6, and y' is a number from 1 to 4 and ammonia or an amine of the general formula: ##STR11## where R' is independently hydrogen or an alkyl (C 1 -C 25 ) radical in the presence of a catalytically effective amount of an acid phosphate salt of a Group IIIB metal at a temperature from about 175° C. to about 400° C. under a pressure sufficient to maintain a substantial amount of the ammonia or amine in the reaction zone.

Claim 23

A process for preparing a noncyclic polyalkylene polyamine which comprises: (a) contacting an alkanolamine compound having an amino group and a primary or secondary hydroxy group of the general formula: ##STR9## where R is hydrogen or a lower alkyl (C 1 -C 4 ) radical, R' is hydrogen or an alkyl (C 1 -C 25 ) radical, x is a number from 2 to 6, and y is a number from 0 to 3 with an alkyleneamine compound having two amino groups of the general formula: ##STR10## where R is a hydrogen or a lower alkyl (C 1 -C 4 ) radical, R' is hydrogen or an alkyl (C 1 -C 25 ) radical, x' is a number from 2 to 6, and y' is a number from 1 to 4 and ammonia or an amine of the general formula: ##STR11## where R' is independently hydrogen or an alkyl (C 1 -C 25 ) radical in the presence of a catalytically effective amount of an acid phosphate salt of a Group IIIB metal at a temperature from about 175° C. to about 400° C. under a pressure sufficient to maintain a substantial amount of the ammonia or amine in the reaction zone.

Claim 24

The process of claim 20 in which the catalyst is a Group IIIB metal monohydrogen phosphate.

Claim 25

The process of claim 20 in which the catalyst is a Group IIIB metal dihydrogen phosphate.

Claim 26

A continuous process for preparing predominantly noncyclic polyalkylene polyamines which comprises (a) adding a charge consisting essentially of ammonia or a primary or secondary amine and an alkanolamine compound having an amino group and a primary or secondary hydroxy group to a reaction zone containing an alkyleneamine compound having two amino groups and a catalytically effective amount of a Group IIIB metal acid phosphate at a temperature sufficient to effect a reaction among the ammonia or amine, the alkanolamine compound and the alkyleneamine compound under a pressure sufficient to maintain a substantial amount of the ammonia or amine in the reaction zone to produce a reaction product stream comprising ammonia or primary or secondary amine, alkanolamine compound, alkyleneamine compound and polyalkylene polyamines, and (b) withdrawing the product stream from the reaction zone and separating it to provide a polyalkylene polyamines stream and ammonia or the primary or secondary amine, alkanolamine compound and alkyleneamine compound which are recycled to the reaction zone.

Claim 27

A continuous process for preparing predominantly noncyclic polyalkylene polyamines which comprises (a) adding a charge consisting essentially of ammonia or a primary or secondary amine and an alkanolamine compound having an amino group and a primary or secondary hydroxy group to a reaction zone containing an alkyleneamine compound having two amino groups and a catalytically effective amount of a Group IIIB metal acid phosphate at a temperature sufficient to effect a reaction among the ammonia or amine, the alkanolamine compound and the alkyleneamine compound under a pressure sufficient to maintain a substantial amount of the ammonia or amine in the reaction zone to produce a reaction product stream comprising ammonia or primary or secondary amine, alkanolamine compound, alkyleneamine compound and polyalkylene polyamines, and (b) withdrawing the product stream from the reaction zone and separating it to provide a polyalkylene polyamines stream and ammonia or the primary or secondary amine, alkanolamine compound and alkyleneamine compound which are recycled to the reaction zone.

Claim 28

The process of claim 23 in which the charge consists essentially of ammonia and monoethanolamine and the alkyleneamine is ethylenediamine.

Claim 29

The process of claim 24 in which the molar ratio of ethylenediamine:monoethanolamine:ammonia in the reaction zone is maintained from 0.75-10:0.5-2:0.35-20 and the pressure is from about 5 to 150 atmospheres.

Claim 30

The process of claim 23 in which the catalyst is a lanthanum acid phosphate.

Claim 31

The process of claim 25 in which the catalyst is a lanthanum acid phosphate.

Claim 32

In a continuous process for the preparation of predominantly noncyclic polyalkylene polyamines which comprises continuously adding a feed comprising an alkanolamine compound having a primary amino group and a primary or secondary hydroxy group and an alkyleneamine compound having two primary amino groups to a reaction zone containing a catalyst to yield a product stream comprising noncyclic polyalkylene polyamines, alkanolamine compound and alkyleneamine compound, separating the desired polyamines from the product stream and recycling the alkanolamine and alkyleneamine compounds to the reaction zone, the method for substantially reducing the amount of alkyleneamine compound in the feed to the reaction zone, which method comprises (a) adding ammonia or a primary or secondary alkylamine to the feed to the reaction zone, (b) using a catalytically effective amount of a Group IIIB metal acid phosphate or as the catalyst, and (c) effecting the reaction under a pressure sufficient to maintain a substantial amount of the ammonia or amine in the reaction zone.

Claim 33

In a continuous process for the preparation of predominantly noncyclic polyalkylene polyamines which comprises continuously adding a feed comprising an alkanolamine compound having a primary amino group and a primary or secondary hydroxy group and an alkyleneamine compound having two primary amino groups to a reaction zone containing a catalyst to yield a product stream comprising noncyclic polyalkylene polyamines, alkanolamine compound and alkyleneamine compound, separating the desired polyamines from the product stream and recycling the alkanolamine and alkyleneamine compounds to the reaction zone, the method for substantially reducing the amount of alkyleneamine compound in the feed to the reaction zone, which method comprises (a) adding ammonia or a primary or secondary alkylamine to the feed to the reaction zone, (b) using a catalytically effective amount of a Group IIIB metal acid phosphate or as the catalyst, and (c) effecting the reaction under a pressure sufficient to maintain a substantial amount of the ammonia or amine in the reaction zone.

Claim 34

The method of claim 28 in which unreacted ammonia or amine is recycled to the reaction zone.

Claim 35

The method of claim 29 in which the alkanolamine compound is monoethanolamine and the alkyleneamine compound is ethylenediamine.

Claim 36

The method of claim 30 in which the molar ratio of ethylenediamine:monoethanolamine:ammonia in the reaction zone is from 0.75-10:0.5-2:0.35-20.

Claim 37

The method of claim 30 in which the catalyst is a lanthanum acid phosphate.

Claim 38

The method of claim 32 in which the pressure is from about 5 to 150 atmospheres.

Claim 39

The method of claim 33 in which the temperature is from 175° C. to 400° C.

Claim 40

The process of claim 1 in which the catalyst is a mixture of the Group IIIB phosphate, monohydrogen phosphate and dihydrogen phosphate.

Claim 41

The process of claim 15 in which the catalyst is a mixture of the Group IIIB phosphate, monohydrogen phosphate and dihydrogen phosphate.

Claim 42

The process of claim 20 in which the catalyst is a mixture of the Group IIIB phosphate, monohydrogen phosphate and dihydrogen phosphate.

Claim 43

The process of claim 23 in which the catalyst is a mixture of the Group IIIB phosphate, monohydrogen phosphate and dihydrogen phosphate.

Claim 44

The process of claim 28 in which the catalyst is a mixture of the Group IIIB phosphate, monohydrogen phosphate and dihydrogen phosphate.