Energy storage flywheel using liquid crystalline polymer tape

Claim 2

A flywheel comprising a diametrically wound unitary tape of a thermotropic liquid crystalline polymer.

Claim 3

The flywheel of claim 1 wherein the tape increases in thickness as a function of the radial distance from the center of the flywheel.

Claim 4

The flywheel of claim 1 wherein the modulus of the tape increases as a function of the radial distance from the center of the flywheel.

Claim 5

The flywheel of claim 1 wherein the tape is heat treated to increase its modulus prior to being wound into a flywheel.

Claim 6

The flywheel of claim 1 wherein particulate ballast is incorporated within the tape during its formation, with decreasing amounts of ballast being incorporated at increasing radial distances from the center of the flywheel.

Claim 7

The flywheel of claim 1 wherein particulate ballast is adhered to the tape prior to winding, the amount of ballast decreasing at increasing radial distances from the center of the flywheel.

Claim 8

The flywheel of claim 1 wherein the thermotropic liquid crystalline polymer has an inherent viscosity of between about 1.0 and about 15 dl./g. when dissolved in a concentration of 0.1 percent by weight of pentafluorophenol at 60° C.

Claim 9

The flywheel of claim 1 wherein the thermotropic liquid crystalline polymer is selected from the group consisting of a wholly aromatic polyester, an aromatic-aliphatic polyester, a wholly aromatic poly(ester-amide), an aromatic aliphatic poly(ester-amide), an aromatic polyazomethine, an aromatic polyester-carbonate, and mixtures of the same.

Claim 10

The flywheel of claim 1, wherein the thermotropic liquid crystalline polymer is selected from the group consisting of a wholly aromatic polyester, a wholly aromatic poly(esteramide), an aromatic-aliphatic poly(ester-amide), and mixtures of the same.

Claim 11

The flywheel of claim 1, wherein the thermotropic liquid crystalline polymer is a melt processable poly(esteramide) capable of forming an anisotropic melt phase at a temperature below approximately 400° C. consisting essentially of recurring moieties I, II, III, and, optionally, IV wherein: ##STR6## ##STR7## where A is a divalent radical comprising at least one aromatic ring or a divalent trans-1,4-cyclohexylene radical; III is --Y--Ar--Z--, where Ar is a divalent radical comprising at least one aromatic ring, Y is O, NH, or NR, and Z is NH or NR, where R is an alkyl group of 1 to 6 carbon atoms or an aryl group; and IV is --O--Ar'--O--, where Ar' is a divalent radical comprising at least one aromatic ring; wherein at least some of the hydrogen atoms present upon the rings optionally may be replaced by substitution selected from the group consisting of an alkyl group of 1 to 4 carbon atoms, an alkoxy group of 1 to 4 carbon atoms, halogen, phenyl, and mixtures thereof, and wherein said poly(ester-amide) comprises approximately 10 to 90 mole percent of moiety I, approximately 5 to 45 mole percent of moiety II, approximately 5 to 45 mole percent of moiety III, and approximately 0 to 40 mole percent of moiety IV.

Claim 12

The flywheel of claim 1, wherein the thermotropic liquid crystalline polymer is a melt processable wholly aromatic polyester capable of forming an anisotropic melt phase at a temperature below approximately 400° C. consisting essentially of the recurring moieties I, II, and III which may include substitution of at least some of the hydrogen atoms present upon an aromatic ring wherein: ##STR8## II is a dioxy aryl moiety of the formula --O--Ar--O-- where Ar is a divalent radical comprising at least one aromatic ring, and III is a dicarboxy aryl moiety of the formula ##STR9## where Ar' is a divalent radical comprising at least one aromatic ring, with said optional substitution if present being selected from the group consisting of an alkyl group of 1 to 4 carbon atoms, an alkoxy group of 1 to 4 carbon atoms, halogen, a phenyl group and mixtures of the foregoing, and wherein said polyester comprises approximately 10 to 90 mole percent of moiety I, approximately 5 to 45 mole percent of moiety II, and approximately 5 to 45 mole percent of moiety III.

Claim 13

The flywheel of claim 1, wherein the thermotropic liquid crystalline polymer is a melt processable wholly aromatic polyester capable of forming a thermotropic melt phase at a temperature below approximately 350° C. consisting essentially of the recurring moieties I and II which may include substitution of at least some of the hydrogen atoms present upon an aromatic ring wherein: ##STR10## with said optional substitution if present being selected from the group consisting of an alkyl group of 1 to 4 carbon atoms, an alkoxy group of 1 to 4 carbon atoms, halogen, phenyl, and mixtures of the foregoing, and wherein said polyester comprises approximately 10 to 90 mole percent of moiety I, and approximately 10 to 90 percent of moiety II.

Claim 14

A process for preparing the flywheel of claim 1 comprising (a) extruding a tape of thermotropic liquid crystalline polymer, (b) winding the tape on a flywheel blank to form a flywheel, and (c) removing the flywheel blank.

Claim 15

The process of claim 13 wherein the tape is slit to an appropriate width as a part of the winding step.

Claim 16

The process of claim 13 wherein the extruded tape is heat treated prior to being wound into a flywheel.

Claim 17

The process of claim 13 wherein particulate ballast is blended with the thermotropic liquid crystalline polymer prior to extrusion.

Claim 18

The process of claim 13 wherein particulate ballast is adhered to the extruded tape prior to being wound into a flywheel.

Claim 19

The process of claim 13 wherein the extruded tape is coated with an adhesive prior to being wound into a flywheel.

Claim 20

The process of claim 13 wherein the extruded tape wound to form the flywheel increases in thickness as a function of the radial distance from the center of the flywheel.