Sulfur plasticization with olefins

Claim 2

A process for plasticizing sulfur to obtain a flexible, elastomeric material which consists essentially of adding to sulfur with thorough mixing at a temperature of from about 115° to about 160° C. from about 10% to about 50% by weight of said sulfur a mixture of dicyclopentadiene and an olefinic material selected from the group of (1) an unsaturated bridge-ring hydrocarbon containing at least two double bonds, (2) a cyclic or acyclic di- or triolefinic terpene, and (3) a hydrocarbon where a cyclic diene is fused to an aromatic ring, wherein said bridge-ring hydrocarbon is selected from the group consisting of: (a) unsaturated derivatives of bicyclo[2.2.1]heptane, contaning at least two double bonds, (b) unsaturated derivatives of bicyclo[2.2.2]octane containing at least two double bonds, (c) unsaturated derivatives of bicyclo[3.2.1.]octane containing at least two double bonds, (d) unsaturated derivatives of bicyclo[3.3.1]nonane containing at least two double bonds, and (e) unsaturated derivatives of bicyclo[3.2.2]nonane containing at least two double bonds; wherein said cyclic or acyclic di- or triolefin terpene is selected from the group consisting of: dipentene, ψ-limonene, 3,8-p-menthadiene, α- and β-phellandiene, α- and γ-terpinene, terpinolene, isoterpinolene, myrcene, ocimene, alloocimene, p-cymene, α- and β-caryophyllene, wherein said hydrocarbon with a cyclic diene fused to an aromatic ring is selected from the group consisting of indene, acenaphthalene and azulene, and wherein the weight ratio of said dicyclopentadiene to said olefinic material is from about 25:75 to about 75:25.

Claim 3

The process of claim 1 wherein the olefinic material is a bridge-ring hydrocarbon.

Claim 4

The process of claim 2 where the hydrocarbon is norbornadiene.

Claim 5

The process of claim 1 where the olefinic material is a hydrocarbon having a cyclic olefin fused to an aromatic ring.

Claim 6

The process of claim 4 wherein the cyclic diolefin is indene.

Claim 7

The process of claim 1 where the olefinic material is a cyclic or acyclic di- or triolefinic terpene.

Claim 8

The process of claim 6 where the terpene is limionene.

Claim 9

The process of claim 6 where the terpene is alloocimene.

Claim 10

The process of claim 6 where the terpene is myrcene.

Claim 11

A flexible, plasticized sulfur composition obtained by adding with agitation a mixture of dicyclopentadiene and an olefinic material to molten sulfur held at a temperature of from about 115° to about 160° C., the weight ratio of the mixture of dicyclopentadiene to olefinic material being from about 25:75 to about 75:25, the amount of said mixture being added to said sulfur being from about 10% to about 50% by weight of said sulfur, and said olefinic material being selected from the group of (1) an unsaturated bridge-ring hydrocarbon containing at least two double bonds, (2) a cyclic or acyclic di- or triolefinic terpene, and (3) a hydrocarbon where a cyclic diene is fused to an aromatic ring, wherein said bridge-ring hydrocarbon is seleced from the group consisting of: (a) unsaturated derivatives of bicyclo[2.2.1]heptane, containing at least two double bonds, (b) unsaturated derivatives of bicyclo[2.2.2]octane containing at least two double bonds, (c) unsaturated derivatives of bicyclo[3.2.1.]octane containing at least two double bonds, (d) unsaturated derivatives of bicyclo[3.3.1]nonane containing at least two double bonds, and (e) unsaturated derivatives of bicyclo[3.2.2]nonane containing at least two double bonds; wherein said cyclic or acyclic di- or triolefinic terpene is selected from the group consisting of: dipentene, -limonene, 3,8-p-menthadiene, α- and β-phellandiene, α- and γ-terpinene, terpinolene, isoterpinolene, myrcene, ocimene, alloocimene, p-cymene, α- and β-caryophyllene and wherein said hydrocarbon with a cyclic diene fused to an aromatic ring is selected from the group consisting of indene, acenaphthalene and azulene.

Claim 12

A flexible, plasticized sulfur composition obtained by adding with agitation a mixture of dicyclopentadiene and an olefinic material to molten sulfur held at a temperature of from about 115° to about 160° C., the weight ratio of the mixture of dicyclopentadiene to olefinic material being from about 25:75 to about 75:25, the amount of said mixture being added to said sulfur being from about 10% to about 50% by weight of said sulfur, and said olefinic material being selected from the group of (1) an unsaturated bridge-ring hydrocarbon containing at least two double bonds, (2) a cyclic or acyclic di- or triolefinic terpene, and (3) a hydrocarbon where a cyclic diene is fused to an aromatic ring, wherein said bridge-ring hydrocarbon is seleced from the group consisting of: (a) unsaturated derivatives of bicyclo[2.2.1]heptane, containing at least two double bonds, (b) unsaturated derivatives of bicyclo[2.2.2]octane containing at least two double bonds, (c) unsaturated derivatives of bicyclo[3.2.1.]octane containing at least two double bonds, (d) unsaturated derivatives of bicyclo[3.3.1]nonane containing at least two double bonds, and (e) unsaturated derivatives of bicyclo[3.2.2]nonane containing at least two double bonds; wherein said cyclic or acyclic di- or triolefinic terpene is selected from the group consisting of: dipentene, -limonene, 3,8-p-menthadiene, α- and β-phellandiene, α- and γ-terpinene, terpinolene, isoterpinolene, myrcene, ocimene, alloocimene, p-cymene, α- and β-caryophyllene and wherein said hydrocarbon with a cyclic diene fused to an aromatic ring is selected from the group consisting of indene, acenaphthalene and azulene.

Claim 13

The sulfur composition of claim 10 obtained by adding a mixture of dicyclopentadiene and norbornadiene to sulfur.

Claim 14

The sulfur composition of claim 10 obtained by adding a mixture of dicyclopentadiene and indene to sulfur.

Claim 15

The sulfur composition of claim 10 obtained by adding a mixture of dicyclopentadiene and limonene to sulfur.

Claim 16

The sulfur composition of claim 10 obtained by adding a mixture of dicyclopentadiene and myrcene to sulfur.