POLYMER OR OLIGOMER FIBERS BY SOLVENT-FREE ELECTROSPINNING

1 . A process for fabricating fibers comprising electrospinning a melt of a self assembling material, wherein the self-assembling material of the fibers comprises oligomers or polymers comprising a supramolecular structure, the oligomers and polymers having repeat units that contain functional groups having directional interactions that are (a) electrostatic interactions (ion-ion, ion-dipole or dipole-dipole) or coordinative bonding (metal-ligand), (b) hydrogen bonding, (c) π-π stacking interactions, or (d) van der Waals forces, or a combination thereof, the supramolecular structure being formed upon a triggering event.

2 . A process according to claim 1 wherein the self-assembling material is selected from the group consisting of a polyester-amide, polyether-amide, polyester-urethane, polyether-urethane, polyether-urea, polyester-urea, or a mixture thereof.

3 . A process according to claim 1 wherein the number average molecular weight (Mn) of the self assembling material is between about 1000 grams per mole (g/mol) and about 30,000 g/mol.

4 . (canceled)

5 . A process according to claim 1 wherein the self assembling material comprises self assembling units comprising multiple hydrogen bonding arrays.

6 - 9 . (canceled)

10 . A process according to claim 5 wherein the self assembling units comprise a bis-amide, bis-urethane or bis-urea unit or their higher oligomers.

11 . A process according to claim 1 wherein the self-assembling material is selected from the group consisting of:

a) a polymer or oligomer comprising repeat units -[H1-AA]- and -[DV-AA]-, where H1 is —R—CO—NH—Ra—NH—CO—R—O— or —R—NH—CO—R—CO—NH—R—O— where Ra is R or a bond, R is independently in each occurrence an aliphatic or heteroaliphatic, alicyclic or heteroalicyclic or aromatic or heteroaromatic group, AA is a —CO—R′—CO—O— where R′ is a bond or an aliphatic group, where DV is -[R″—O]- and R″ is an aliphatic or heteroaliphatic, alicyclic or heteroalicyclic or aromatic or heteroaromatic group;

b) a polymer or oligomer comprising repeat units -[H1-AA]-, -[DV-AA]-, and -[D2-O-AA]-, where D2 is independently in each occurrence an aliphatic or heteroaliphatic, alicyclic or heteroalicyclic or aromatic or heteroaromatic group;

c) a polymer or oligomer comprising repeat units -[H1-AA]-, -[R—O-AA]-, and -M-(AA) n -, wherein M is an n valent organic moiety, and n is 3 or more;

d) a polymer or oligomer comprising repeat units -[H1-AA]-, -[R—O-AA]-, and -PA-(CO—O—R) n —, wherein PA is an n valent organic moiety, and n is 3 or more;

e) a polymer or oligomer comprising repeat units -[H2-D]-, and -[R—O-AA]-, where H2 is —CO—R—CO—NH—R—NH—CO—R—CO—O— where R is independently in each occurrence an aliphatic or heteroaliphatic, alicyclic or heteroalicyclic or aromatic or heteroaromatic group, and where D is -[R—O]-;

f) a polymer or oligomer comprising repeat units -[H2-D]-, -[R—O-AA]-, and -M-(AA) n -, where H2 is —CO—R—CO—NH—R—NH—CO—R—CO—O— where R is independently in each occurrence an aliphatic or heteroaliphatic, alicyclic or heteroalicyclic or aromatic or heteroaromatic group, and where D is -[R—O]-;

g) a polymer or oligomer comprising repeat units -[H2-AA]-, -[R—O-AA]-, and -PA-(COOR)n-;

h) a polymer or oligomer having the formula HO-D1-O—[—CO-AA1,2-CO—O-D1-O-]x-[CO-AA1,2-CO—O-AD-O]y-H, wherein O-D1-O represents the residual of a diol functionality, wherein CO-AA1,2-CO represents the residual of an aliphatic dicarboxylic acid functionality or a high boiling point diacid ester functionality, wherein O-AD-O represents the residual of a polyamide diol functionality, wherein x and y are the number of repeat units within the polymer block inside the brackets;

i) a polymer or oligomer comprising repeat units -[H2-D]-, -[H2-O-D2]-, [D-AA]-, and -[D2-O-AA]-;

j) a polymer or oligomer having the formula HO-D1-O—[—CO-AA1,2-CO—O-D1-O-]x-[CO-AA1,2-CO—O—CO-DD-CO]y-OH, wherein O—CO-DD-CO—O represents the residual of a diamide diacid functionality; and

k) mixtures thereof.

12 . A process according to claim 11 , wherein the self-assembling material is selected from the group consisting of the polymer or oligomer of a), b), c), d), f), g), h), i), j) and mixtures thereof.

13 - 19 . (canceled)

20 . A process according to claim 11 wherein the polymer or oligomer comprises the formula:

—[C(O)R′C(O)O—R″O] x —[C(O)R′C(O)O—RC(O)N(H)RaN(H)C(O)RO] y —

wherein R is independently in each occurrence an aliphatic or heteroaliphatic, alicyclic or heteroalicyclic or aromatic or heteroaromatic group;

R′ is a bond or an aliphatic group;

R″ is an aliphatic or heteroaliphatic, alicyclic or heteroalicyclic or aromatic or heteroaromatic group;

Ra is a bond or is an aliphatic or heteroaliphatic, alicyclic or heteroalicyclic or aromatic or heteroaromatic group; and

the number average molecular weight of the polymer or oligomer is between about 1000 g/mol and about 30,000 g/mol.

21 . A process according to claim 11 wherein the polymer or oligomer is of the formula:

wherein

p, q, and r are independently 2, 3, 4, 5, 6 or 8;

n is 2-6 and

the number average molecular weight of the polymer or oligomer is between about 1000 g/mol and 30,000 g/mol.

22 . A process according to claim 21 wherein n is 2.

23 . A process according to claim 21 wherein the polymer or oligomer is of the formula:

24 - 29 . (canceled)

30 . A process according to claim 20 wherein the number average molecular weight of the polymer or oligomer is between about 2000 g/mol and about 20,000 g/mol.

31 . (canceled)

32 . A process according to claim 1 , wherein the fibers have an average diameter of about 1000 nanometers or less.

33 . A process according to claim 1 , wherein viscosity of the self assembling material is less than 100 pascal-seconds (Pa.sec.) at from above Tm up to about 40 degrees Celsius (° C.) above Tm.

34 - 39 . (canceled)

40 . A process according to claim 1 , wherein the fibers have an average diameter of from about 30 nm to about 1000 nanometers and the fibers are produced at a rate, expressed in grams per minute (g/min), at least 2 times a solvent-normalized rate, expressed in g/min, of producing corresponding diameter fibers from the self assembling material with a solvent-based electrospinning process.

41 . Fibers fabricated by the process according to claim 1 .

42 . Fibers fabricated according to the process of claim 1 having an average diameter of about 30 nm to about 1000 nm

43 - 46 . (canceled)

47 . A filtration non-woven comprising fibers as in claim 41 .

48 . A filtration non-woven as in claim 47 , the filtration non-woven being for air or gas filtration.

49 . (canceled)

50 . (canceled)

51 . A process as in claim 1 , wherein the oligomers or polymers have a statistical distribution of the repeat units.