Aromatic thermoset resins
Processes for chemically treating mixed aromatic feedstock to form thermoset aromatic resins are provided. The thermoset materials possess high compressive strength and find particular use in load-bearing applications, for example, infrastructure applications, as proppants, and as components in composite materials.
1 . A method of making a thermoset material from a mixed aromatic feedstock comprising:
contacting a linker agent and a catalyst with a mixed aromatic feedstock at a temperature effective to react the linker agent with molecules in the mixed aromatic feedstock,
wherein the contacting is conducted at a first pressure for a first time; and curing reaction products formed during the first time at a second pressure for a second time,
wherein the second pressure is higher than the first pressure;
wherein the linker agent contains at least two different functional groups that can react with the molecules in the mixed aromatic feedstock; and
wherein the thermoset material has a compressive strength greater than about 100 MPa, when measured according to ASTM D695.
2 . A method according to claim 1 , wherein the mixed aromatic feedstock and linker agent are reacted at the first pressure until before gel point is reached, at which time the pressure is raised to the second pressure.
3 . A method according to claim 1 , wherein the first pressure is about 2.0 bar (200 kPa) or less.
4 . A method according to claim 1 , wherein the linker agent and molecules in the mixed aromatic feedstock are reacted for the first time at a temperature between about 20° C. and about 400° C.
5 . A method according to claim 1 , wherein the reaction products are cured for the second time at a temperature between about 100° C. and about 400° C.
6 . A method according to claim 1 , wherein the linker agent has the structure of Formula 1:
wherein the circle represent an aromatic hydrocarbon or aromatic heterocyclic moiety; FG (functional group) is, independently, aldehyde, vinyl, halogen, hydroxyl, acyl halide, tosylate, mesylate, carboxylic acid; each X, when present, is, independently, alkylene, cycloalkylene, or arylene bonded to a ring carbon atom of the aromatic hydrocarbon or aromatic heterocyclic moiety; n is an integer in the range of 1 to 5.
7 . A method according to claim 1 , wherein the linker agent has the structure of Formula 2:
(Formula) wherein FG (functional group) is, independently, aldehyde, vinyl, halogen, hydroxyl, acyl halide, tosylate, mesylate, carboxylic acid; each X, when present, is, independently, alkylene, cycloalkylene, or arylene; each R is, independently, H or alkyl, n is an integer in the range of 1 to 5 and m is 5-n.
8 . A method according to claim 1 , wherein the linker agent has the structure of Formula 3:
(Formula 3) wherein FG (functional group) is, independently, aldehyde, vinyl, halogen, hydroxyl, acyl halide, tosylate, mesylate, carboxylic acid; each X, when present, is, independently, alkylene, cycloalkylene, or arylene; each R is, independently, H or alkyl; y1+y2 is an integer between 2 and 8; and m1+m2=8−(y1+y2).
9 . A method according to claim 1 , wherein the linker agent has the structure of Formula 4:
(Formula 4) wherein FG (functional group) is, independently, aldehyde, vinyl, halogen, hydroxyl, acyl halide, tosylate, mesylate, carboxylic acid; each X, when present, is, independently, alkylene, cycloalkylene or arylene; each R is, independently, H or alkyl; y1+y2 is an integer between 2 and 10; and m1+m2=10−(y1+y2).
10 . A method according to claim 1 , wherein the linker agent is present in the amount of 1% to 200% by weight, based on the weight of the mixed aromatic feedstock.
11 . A method according to claim 1 , wherein the method is performed without any solvent.
12 . A method according to claim 1 , wherein the mixed aromatic feedstock has a hydrogen to carbon (H/C) ratio less than 1.2.
13 . A method according to claim 1 , wherein the mixed aromatic feedstock has an aromatic content of greater than 50% by weight.