Diamino disulfide curatives for polyurethanes

Claim 2

A cured polyurethane composition comprising the reaction product of (A) an organic polyisocyanate, (B) a polymeric diol, and (C) an organic diamino disulfide selected from the group consisting of a. diamino diphenyl disulfides with amino groups located in different phenyl radicals and having the amino groups located in positions ortho to the disulfide group, b. diamino dinaphthyl disulfides having melting points below 150° C., and with amino groups located in different naphthyl radicals, c. organic diamino disulfides having the structure NH 2 --Ar--S--S--R'--NH 2 or NH 2 --R'--S-- S--R'--NH 2 in which Ar is an aryl radical and R' is a tertiary aliphatic or cycloaliphatic radical in which the amino group is attached to the tertiary carbon atom, and d. organic diamino aryl disulfides in which one of the radicals attached to the disulfide group is a diaminoaryl radical and the other radical attached to the disulfide group is either an aryl or a lower alkyl radical, in which said (C) may have been reacted simultaneously with said (A) and (B), or in which said (A) and (B) may have been reacted together to form a polyurethane prepolymer before reaction with said (C).

Claim 3

A composition according to claim 1 in which said (C) is an ortho, ortho'-diaminodiaryl disulfide.

Claim 4

A composition according to claim 2 in which said (C) is 2,2'-diaminodiphenyl disulfide.

Claim 5

A composition according to claim 2 in which said (C) is 2,2'-diamino-4,4'-dichlorodiphenyl disulfide.

Claim 6

A composition according to claim 2 in which said (C) is 2,2'-diamino-4,4'-di-lower-alkyldiphenyl disulfide.

Claim 7

A composition according to claim 1 in which said (C) is bis [8-aminonaphthyl(1)] disulfide.

Claim 8

A composition according to claim 1 in which said (C) is bis [1-aminonaphthyl(2)] disulfide.

Claim 9

A composition according to claim 1 in which said (C) has the structure ##SPC2## wherein Y is an aryl or lower alkyl radical.

Claim 10

A composition according to claim 1 in which the ratio of NCO groups in said (A) to the OH groups in said (B) ranges from 1.75 to 2.50, and the ratio of the sum of the OH groups in said (B) plus NH 2 groups in said (C) to the NCO groups in said (A) ranges from 0.50 to 0.95.

Claim 11

A curative comprising a blend consisting of (a) an organic diamino disulfide selected from the group consisting of: 1. diamino diphenyl disulfides with amino groups located in different phenyl radicals and having the amino groups located in positions ortho to the disulfide group, 2. diamino dinaphthyl disulfides having melting points below 150° C., and with amino groups located in different naphthyl radicals, 3. organic diamino disulfides having the structure NH 2 --Ar--S--S--R'--NH 2 or NH 2 --R'--S--S--R'--NH 2 in which Ar is an aryl radical and R' is a tertiary aliphatic or cycloaliphatic radical in which the amino group is attached to the tertiary carbon atom, and 4. organic diamino aryl disulfides in which one of the radicals attached to the disulfide group is a diaminoaryl radical and the other radical attached to the disulfide group is either an aryl or a lower alkyl radical, and (b) an aromatic diamine.

Claim 12

A curative comprising a blend consisting of (a) an organic diamino disulfide selected from the group consisting of: 1. diamino diphenyl disulfides with amino groups located in different phenyl radicals and having the amino groups located in positions ortho to the disulfide group, 2. diamino dinaphthyl disulfides having melting points below 150° C., and with amino groups located in different naphthyl radicals, 3. organic diamino disulfides having the structure NH 2 --Ar--S--S--R'--NH 2 or NH 2 --R'--S--S--R'--NH 2 in which Ar is an aryl radical and R' is a tertiary aliphatic or cycloaliphatic radical in which the amino group is attached to the tertiary carbon atom, and 4. organic diamino aryl disulfides in which one of the radicals attached to the disulfide group is a diaminoaryl radical and the other radical attached to the disulfide group is either an aryl or a lower alkyl radical, and (b) an aromatic diamine.

Claim 13

The composition of claim 10 in which said (a) is a diaminodiaryl disulfide.

Claim 14

The composition of claim 11 in which the amount of (a) varies from 25 to 99 percent by weight and the amount of (b) varies from 1 to 75 percent by weight of the sum of the weights of (a) plus (b).

Claim 15

The composition of claim 11 in which said (a) is 2,2'-diaminodiphenyl disulfide.

Claim 16

The composition of claim 11 in which said (a) is 2,2'-diamino-4,4'-dichlorodiphenyl disulfide.

Claim 17

The composition of claim 11 in which said (b) is selected from the group consisting of m-phenylene diamine, 2,4-tolylene diamine, and methylene bis(aniline).

Claim 18

A curative comprising a blend consisting of (a) an organic diamino disulfide selected from the group consisting of: 1. diamino diphenyl disulfides with amino groups located in different phenyl radicals and having the amino groups located in positions ortho to the disulfide group, 2. diamino dinaphthyl disulfides having melting points below 150° C., and with amino groups located in different naphthyl radicals, 3. organic diamino disulfides having the structure NH 2 --Ar--S--S--R'--NH 2 or NH 2 --R'--S--S--R'--NH 2 in which Ar is an aryl radical and R' is a tertiary aliphatic or cycloaliphatic radical in which the amino group is attached to the tertiary carbon atom, 4. organic diamino aryl disulfides in which one of the radicals attached to the disulfide group is a diaminoaryl radical and the other radical attached to the disulfide group is either an aryl or a lower alkyl radical, and 5. substituted para, para' diamino diphenyl disulfides having substituents selected from the group consisting of lower alkyl and lower alkoxy radicals, and (b) a diol.

Claim 19

A curative comprising a blend consisting of (a) an organic diamino disulfide selected from the group consisting of: 1. diamino diphenyl disulfides with amino groups located in different phenyl radicals and having the amino groups located in positions ortho to the disulfide group, 2. diamino dinaphthyl disulfides having melting points below 150° C., and with amino groups located in different naphthyl radicals, 3. organic diamino disulfides having the structure NH 2 --Ar--S--S--R'--NH 2 or NH 2 --R'--S--S--R'--NH 2 in which Ar is an aryl radical and R' is a tertiary aliphatic or cycloaliphatic radical in which the amino group is attached to the tertiary carbon atom, 4. organic diamino aryl disulfides in which one of the radicals attached to the disulfide group is a diaminoaryl radical and the other radical attached to the disulfide group is either an aryl or a lower alkyl radical, and 5. substituted para, para' diamino diphenyl disulfides having substituents selected from the group consisting of lower alkyl and lower alkoxy radicals, and (b) a diol.

Claim 20

The composition of claim 16 in which said (a) is a diaminodiaryl disulfide and said (b) is a polymeric diol.

Claim 21

The composition of claim 17 in which said (a) is 2,2'-diaminodiphenyl disulfide.

Claim 22

The composition of claim 17 in which said (a) is 4,4'-diaminodiphenyl disulfide.

Claim 23

The composition of claim 17 in which said (a) is 2,2'-diamino-4,4'-dichlorodiphenyl disulfide.

Claim 24

The composition of claim 17 in which said (a) is a substituted 4,4'-diaminodiphenyl disulfide, with substituents selected from the group consisting of chloro, bromo, lower alkyl and lower alkoxy radicals.

Claim 25

The composition of claim 17 in which said (a) constitutes from 5 to 99 percent by weight and said (b) constitutes from 1 to 95 percent by weight of the sum of the weights of (a) plus (b).

Claim 26

A curative comprising a blend consisting of (a) an organic diamino disulfide selected from the group consisting of: 1. diamino diphenyl disulfides with amino groups located in different phenyl radicals and having the amino groups located in positions ortho to the disulfide group, 2. diamino dinaphthyl disulfides having melting points below 150° C., and with amino groups located in different naphthyl radicals, 3. organic diamino disulfides having the structure NH 2 --Ar--S--S--R'--NH 2 or NH 2 --R'--S--S--R'--NH 2 in which Ar is an aryl radical and R' is a tertiary aliphatic or cycloaliphatic radical in which the amino group is attached to the tertiary carbon atom, 4. organic diamino aryl disulfides in which one of the radicals attached to the disulfide group is a diaminoaryl radical and the other radical attached to the disulfide group is either an aryl or a lower alkyl radical, and 5. substituted para, para'-diamino diphenyl disulfides having substituents selected from the group consisting of lower alkyl and lower alkoxy radicals, (b) an aromatic diamine, and (c) a diol.

Claim 27

A curative comprising a blend consisting of (a) an organic diamino disulfide selected from the group consisting of: 1. diamino diphenyl disulfides with amino groups located in different phenyl radicals and having the amino groups located in positions ortho to the disulfide group, 2. diamino dinaphthyl disulfides having melting points below 150° C., and with amino groups located in different naphthyl radicals, 3. organic diamino disulfides having the structure NH 2 --Ar--S--S--R'--NH 2 or NH 2 --R'--S--S--R'--NH 2 in which Ar is an aryl radical and R' is a tertiary aliphatic or cycloaliphatic radical in which the amino group is attached to the tertiary carbon atom, 4. organic diamino aryl disulfides in which one of the radicals attached to the disulfide group is a diaminoaryl radical and the other radical attached to the disulfide group is either an aryl or a lower alkyl radical, and 5. substituted para, para'-diamino diphenyl disulfides having substituents selected from the group consisting of lower alkyl and lower alkoxy radicals, (b) an aromatic diamine, and (c) a diol.

Claim 28

The composition of claim 23 in which said (a) is a diaminodiaryl disulfide.

Claim 29

The composition of claim 23 in which said (c) is a polymeric diol.

Claim 30

The composition of claim 24 in which said (a) is 2,2'-diaminodiphenyl disulfide.

Claim 31

The composition of claim 24 in which said (a) is 2,2'-diamino-4,4'-dichlorodiphenyl disulfide.

Claim 32

The composition of claim 24 in which said (a) is a substituted 4,4'-diaminodiphenyl disulfide, with substituents selected from the group consisting of chloro, bromo, lower alkyl, and lower alkoxy radicals.

Claim 33

The composition of claim 23 in which the amount of (c) constitutes from 1 to 95 percent of the combined weights of (a) plus (b) plus (c), the amount of (a) plus (b) constitutes from 5 to 99 percent of the combined weights of (a) plus (b) plus (c), the amount of (a) constitutes from 25 to 99 percent of the combined weights of (a) plus (b), and the amount of (b) constitutes from 1 to 75% of the combined weights of (a) plus (b).

Claim 34

The process of producing a polyurethane composition which comprises intimately admixing a polyurethane prepolymer having isocyanato terminal groups with an organic diamino disulfide curative selected from the group consisting of: a. diamino diphenyl disulfides with amino groups located in different phenyl radicals and having the amino groups located in positions ortho to the disulfide group, b. diamino dinaphthyl disulfides having melting points below 150° C., and with amino groups located in different naphthyl radicals, c. organic diamino disulfides having the structure NH 2 --Ar--S--S--R'--NH 2 or NH 2 --R'--S--S--R'--NH 2 in which Ar is an aryl radical and R' is a tertiary aliphatic or cycloaliphatic radical in which the amino group is attached to the tertiary carbon atom, d. organic diamino aryl disulfides in which one of the radicals attached to the disulfide group is a diaminoaryl radical and the other radical attached to the disulfide group is either an aryl or a lower alkyl radical, and e. 3,5,3',5'-tetra-lower-alkyl-4,4'-diaminodiphenyl disulfides, in an amount such that the stoichiometric ratio of amino groups to isocyanato groups ranges from 0.50 to 0.90 and allowing the reaction mixture to cure by maintaining a temperature ranging from room temperature to 95° C.

Claim 35

The process of producing a polyurethane composition which comprises intimately admixing a polyurethane prepolymer having isocyanato terminal groups with an organic diamino disulfide curative selected from the group consisting of: a. diamino diphenyl disulfides with amino groups located in different phenyl radicals and having the amino groups located in positions ortho to the disulfide group, b. diamino dinaphthyl disulfides having melting points below 150° C., and with amino groups located in different naphthyl radicals, c. organic diamino disulfides having the structure NH 2 --Ar--S--S--R'--NH 2 or NH 2 --R'--S--S--R'--NH 2 in which Ar is an aryl radical and R' is a tertiary aliphatic or cycloaliphatic radical in which the amino group is attached to the tertiary carbon atom, d. organic diamino aryl disulfides in which one of the radicals attached to the disulfide group is a diaminoaryl radical and the other radical attached to the disulfide group is either an aryl or a lower alkyl radical, and e. 3,5,3',5'-tetra-lower-alkyl-4,4'-diaminodiphenyl disulfides, in an amount such that the stoichiometric ratio of amino groups to isocyanato groups ranges from 0.50 to 0.90 and allowing the reaction mixture to cure by maintaining a temperature ranging from room temperature to 95° C.

Claim 36

The process of claim 30 in which said organic diamino disulfide is 2,2'-diaminodiphenyl disulfide.

Claim 37

The process of claim 30 in which said organic diamino disulfide is 2,2'-diamino-4,4'-dichlorodiphenyl disulfide.

Claim 38

The process of claim 30 in which said organic diamino disulfide is a mixture containing 2,2'-diaminodiphenyl disulfide.

Claim 39

The cured composition prepared according to the process of claim 30.

Claim 40

A cured polyurethane composition comprising the reaction product of (A) an organic polyisocyanate, (B) a polymeric diol, and (C) a mixture of 2,2'-diaminodiphenyl disulfide and 4,4'-diaminodiphenyl disulfide, in which said (C) may have been reacted simultaneously with said (A) and (B), or in which said (A) and (B) may have been reacted together to form a polyurethane prepolymer before reaction with said (C).

Claim 41

A cured polyurethane composition comprising the reaction product of (A) an organic polyisocyanate, (B) a polymeric diol, and (C) a mixture of 2,2'-diaminodiphenyl disulfide and 4,4'-diaminodiphenyl disulfide, in which said (C) may have been reacted simultaneously with said (A) and (B), or in which said (A) and (B) may have been reacted together to form a polyurethane prepolymer before reaction with said (C).

Claim 42

A cured polyurethane composition comprising the reaction product of (A) an organic polyisocyanate, (B) a polymeric diol, and (C) a mixture of 2,2'-diaminodiphenyl disulfide and substituted 4,4'-diaminodiphenyl disulfides with substituents being selected from the group consisting of chloro, bromo, lower alkyl and lower alkoxy radicals, in which said (C) may have been reacted simultaneously with said (A) and (B), or in which said (A) and (B) may have been reacted together to form a polyurethane prepolymer before reaction with said (C).

Claim 43

A cured polyurethane composition comprising the reaction product of (A) an organic polyisocyanate, (B) a polymeric diol, and (C) a mixture of 2,2'-diaminodiphenyl disulfide and substituted 4,4'-diaminodiphenyl disulfides with substituents being selected from the group consisting of chloro, bromo, lower alkyl and lower alkoxy radicals, in which said (C) may have been reacted simultaneously with said (A) and (B), or in which said (A) and (B) may have been reacted together to form a polyurethane prepolymer before reaction with said (C).

Claim 44

The process of producing a polyurethane composition which comprises reacting (A) a polymeric polyol, (B) an organic polyisocyanate and (C) an organic diamino disulfide selected from the group consisting of a. diamino diphenyl disulfides with amino groups located in different phenyl radicals and having the amino groups located in positions ortho to the disulfide group, b. diamino dinaphthyl disulfides having melting points below 150° C., and with amino groups located in different naphthyl radicals, c. organic diamino disulfides having the structure NH 2 --Ar--S--S--R'--NH 2 or NH 2 --R'--S--S--R'--NH 2 in which Ar is an aryl radical and R' is a tertiary aliphatic or cycloaliphatic radical in which the amino group is attached to the tertiary carbon atom, d. organic diamino aryl disulfides in which one of the radicals attached to the disulfide group is a diaminoaryl radical and the other radical attached to the disulfide group is either an aryl or a lower alkyl radical, and e. 3,5,3',5'-tetra-lower-alkyl-4,4'-diaminodiphenyl disulfides, with the amounts of (A), (B), and (C) being such that the stoichiometric ratio of amino groups to isocyanato groups ranges from 0.50 to 0.90 and allowing the reaction mixture to cure in the presence of a catalyst for the reaction of isocyanato groups with hydroxyl groups.

Claim 45

The process of producing a polyurethane composition which comprises reacting (A) a polymeric polyol, (B) an organic polyisocyanate and (C) an organic diamino disulfide selected from the group consisting of a. diamino diphenyl disulfides with amino groups located in different phenyl radicals and having the amino groups located in positions ortho to the disulfide group, b. diamino dinaphthyl disulfides having melting points below 150° C., and with amino groups located in different naphthyl radicals, c. organic diamino disulfides having the structure NH 2 --Ar--S--S--R'--NH 2 or NH 2 --R'--S--S--R'--NH 2 in which Ar is an aryl radical and R' is a tertiary aliphatic or cycloaliphatic radical in which the amino group is attached to the tertiary carbon atom, d. organic diamino aryl disulfides in which one of the radicals attached to the disulfide group is a diaminoaryl radical and the other radical attached to the disulfide group is either an aryl or a lower alkyl radical, and e. 3,5,3',5'-tetra-lower-alkyl-4,4'-diaminodiphenyl disulfides, with the amounts of (A), (B), and (C) being such that the stoichiometric ratio of amino groups to isocyanato groups ranges from 0.50 to 0.90 and allowing the reaction mixture to cure in the presence of a catalyst for the reaction of isocyanato groups with hydroxyl groups.

Claim 46

The process of claim 37 in which said catalyst is selected from the group consisting of dialkyltin diacylates and stannous diacylates.