POROUS MATERIALS FROM COMPLEX BLOCK COPOLYMER ARCHITECTURES
Self-assembled porous block copolymer materials with a complex block copolymer architecture, methods of preparing, uses for separation and detection, and devices for using as such. The porous materials contain at least one of macro, meso, or micro pores, at least some of which are isoporous, and include at least one block copolymer with at least two chemically distinct blocks, which further comprises a complex architecture such as: multiple distinct monomers in or between blocks, branching, crosslinking, or ring architectures.
1 . A self-assembled polymer material containing at least one of macro, meso, or micro pores, at least some of which are isoporous, comprising a block copolymer or block copolymers (BCPs), with at least two chemically distinct blocks, which further comprises a complex architecture.
2 . The material of claim 1 wherein at least a portion of the material is a block copolymer containing more than one monomer/chemistry/configuration/structure/composition in at least one block or adjacent to at least one block.
3 . The material of claim 1 wherein at least a portion of the material is a diblock copolymer, triblock copolymer, or higher order (i.e. tetrablock, pentablock, etc.) with more than one monomer/chemistry/configuration/structure/composition in at least one block or adjacent to at least one block.
4 . The material of claim 1 , wherein the material has mesopores comprising a diameter of about 1 nm to about 200 nm.
5 . The material of claim 1 , wherein at least one block copolymer has an M n of about 1×10 3 to about 1×10 7 g/mol.
6 . The material of claim 1 , wherein at least one block copolymer has a PDI of 1.0 to 3.0.
7 . The material of of claim 1 , wherein at least one block of the BCP has at least one of the following properties:
a. Low T g (25° C. or less)
b. High T g (more than 25° C.)
c. Hydrophilic
d. Hydrophobic
e. Chemically resistant
f. Chemically responsive
g. Chemically functional
8 . The material of claim 1 wherein at least a portion of the material comprises at least one unit of one of the following polymer blocks or derivatives thereof:
a. Poly(butadiene)
b. Poly(isobutylene)
c. Poly(isoprene)
d. Poly(ethylene)
e. Poly(styrene)
f. Poly(methyl acrylate)
g. Poly(butyl methacrylate)
h. Poly(ethersulfone)
i. Poly(methyl methacrylate)
j. Poly(n-butyl acrylate)
k. Poly(2-hydroxyethyl methacrylate)
l. Poly(glycidyl methacrylate)
m. Poly(acrylic acid)
n. Poly(acrylamide)
o. Poly(sulfone)
p. Poly(vinylidene fluoride)
q. Poly(N,N-dimethylacrylamide)
r. Poly(2-vinylpyridine)
s. Poly(3-vinylpyridine)
t. Poly(4-vinylpyridine)
u. Poly(ethylene glycol)
v. Poly(propylene glycol)
w. Poly(vinyl chloride)
x. Poly(tetrafluoroethylene)
y. Poly(ethylene oxide)
z. Poly(propylene oxide)
aa. Poly(N-isopropylacrylamide)
bb. Poly(dimethylaminoethyl methacrylate)
cc. Poly(amic acid)
dd. Poly(dimethylsiloxane)
ee. Poly(lactic acid)
ff. Poly(isocyanate)
gg. Poly(ethyl cyanoacrylate)
hh. Poly(acrylonitrile)
ii. Poly(hydroxystyrene)
jj. Poly(methylstyrene)
kk. Poly(ethyleneimine)
ll. Poly(styrene sulfonate)
mm. Poly(allylamine hydrochloride)
nn. Poly(pentafluorostyrene)
oo. Poly(2-(perfluorohexyl)ethyl methacrylate)
pp. Poly(methacrylic acid)
qq. Poly(ethylene sulfide)
rr. Poly(propylene sulfide)
9 . A method of preparing the material of claim 1 , comprising:
a. Dissolution of polymer in at least one chemical solvent
b. Dispensing polymer solution onto a substrate or mold, or through a die or template
c. Removal of at least a portion of chemical solvent
d. Exposure to a nonsolvent causing precipitation of at least a portion of the polymer
e. Optionally, a wash step
10 . The method of claim 9 wherein at least a portion of the chemical solvent is from one of the following classes:
a. Alcohol,
b. Aldehyde,
c. Alkane,
d. Amide,
e. Amine,
f. Cyclic aromatic,
g. Carboxylic acid,
h. Ester,
i. Ether,
j. Ketone,
k. Lactam,
l. Nitrile,
m. Organohalide,
n. Polyol,
o. Sulfone, or
p. Sulfoxide
11 . The method of claim 9 wherein at least a portion of the chemical solvent contains at least one of the following or its derivatives:
a. Acetone,
b. Acetaldehyde,
c. Methanol,
d. Ethanol,
e. Ethyl acetate,
f. Dimethoxyethane,
g. Hexane,
h. Chloroform,
i. Dichloromethane,
j. Acetonitrile,
k. Tetrahydrofuran,
l. Cyclohexane,
m. Benzene,
n. Toluene,
o. Dimethyl sulfoxide,
p. Dimethylformamide,
q. Dimethylacetamide,
r. N-Methyl-2-pyrrolidone,
s. Pyridine,
t. 1,4-Dioxane,
u. Acetic acid,
v. Formic acid, or
w. Propanol
x. Sulfolane
12 . The method of claim 9 wherein the BCP solution further comprises at least one additional macromolecule or a small molecule.
13 . A process separating or detecting an analyte of interest by contacting a medium containing the analyte of interest with at least one material of claim 1 .
14 . A process using at least one material of claim 1 for separation or filtration of liquids or gases.
15 . A process using at least one material of claim 1 for the filtration, separation, or removal of one or more viruses from a liquid or gas.
16 . The material of claim 1 wherein the material comprises more than one BCP.
17 . The material of claim 1 wherein at least a portion of at least one BCP comprises more than one distinct monomer type in at least one block, between blocks, or at the end of at least one block.
18 . The material of claim 1 wherein at least a portion of at least one BCP is branched.
19 . The material of claim 1 wherein at least a portion of at least one BCP is crosslinked.
20 . The material of claim 1 wherein at least a portion of at least one BCP is a ring architecture.