US2023250373A9PendingUtilityA9
Stillage solids concentration
Est. expiryFeb 18, 2036(~9.5 yrs left)· nominal 20-yr term from priority
C12F 3/10B01D 21/01C08F 220/56C08F 222/22B01D 17/0217B01D 17/047Y02E50/10
63
PatentIndex Score
0
Cited by
0
References
0
Claims
Abstract
Stillage solids concentration methods are disclosed wherein a solids concentration aid is added to a process stream mixture in a corn to ethanol process. The solids concentration aid may comprise a cationic polymer coagulant or flocculant or both, a starch based coagulant or flocculant or a biologically derived (i.e., plant or animal origin) coagulant or flocculant. Acrylamide/quaternary ammonium copolymers and homopolymeric polydiallyldimethyl ammonium chloride polymers are noteworthy examples of suitable solids concentration aids.
Claims
exact text as granted — not AI-modified1 . (canceled)
2 . A method for concentrating solids in a corn to ethanol process wherein oil and solids are present in a process stream mixture, said method comprising adding to said process stream mixture an effective amount of a solids concentration aid, said solids concentration aid comprising a cationic polymer coagulant or flocculant or both.
3 . (canceled)
4 . A method for concentrating solids in a corn to ethanol process wherein oil and solids are present in a process stream mixture, said method comprising adding to said process stream mixture an effective amount of a solids concentration aid, wherein said solids concentration aid comprises a cationic polymer.
5 . The method as recited in claim 4 , wherein said cationic polymer comprises:
i) copolymers having monomeric repeat units of Formulae I and II
wherein x:y is within the rage of 95:5 to 5:95; R 1 and R 2 may be the same or different and are chosen form H, and CH 3 ; Q is —C(O)O—, —OC(O)—, or —C(O)NH—, R 3 is branched or linear (C 1 -C 4 ) alkylene, R 4 , R 5 , and R 6 are each independently chosen from H, C 1 -C 4 linear or branched alkyl, or a C 5 -C 8 aromatic or alkylaromatic group, A is an anion selected from Cl − , Br − , HSO 4 − or MeOSO 3 − wherein Me is methyl; or
viii) homopolymers of diallyl dialkyl ammonium chloride.
6 . The method as recited in claim 5 , wherein said cationic polymer i) is present, said cationic polymer i) comprising acrylamide and one or more co-monomeric repeat unit chosen from AETAC, MATAC, METAC, and AEDBAC.
7 . The method as recited in claim 6 , wherein said cationic polymer i) is present in an amount of 1-10,000 ppm based upon the weight of said process stream mixture.
8 . The method as recited claim 7 , wherein said cationic copolymer i) is acrylamide/AETAC.
9 . The method as recited claim 7 , wherein said cationic copolymer i) is acrylamide/MATAC.
10 . The method as recited claim 7 , wherein said cationic copolymer i) is acrylamide/METAC.
11 . The method as recited claim 7 , wherein said cationic copolymer i) is acrylamide/AEDBAC.
12 . The method as recited claim 7 , wherein said cationic copolymer i) is acrylamide/AETAC/AEDBAC.
13 . The method as recited claim 4 , wherein said cationic polymer viii) is present.
14 . The method as recited claim 13 , wherein said cationic polymer viii) is homopolymeric polydiallyldimethyl ammonium chloride—(poly DADMAC).
15 . The method as recited claim 13 , wherein said cationic polymer i) is also present.
16 . The method as recited claim 15 , wherein said cationic polymer i) comprises acrylamide and at least one co-monomeric repeat unit chosen from AETAC, MATAC, METAC, and AEDBAC.
17 - 19 . (canceled)Join the waitlist — get patent alerts
Track US2023250373A9 — get alerts on status changes and closely related new filings.
We store only your email — no account needed. See our privacy policy.