US2019009247A1PendingUtilityA1
Sorbent comprising carbon and nitrogen and methods of using the same
Assignee: MIDWEST ENERGY EMISSIONS CORPPriority: Mar 6, 2013Filed: Sep 13, 2018Published: Jan 10, 2019
Est. expiryMar 6, 2033(~6.6 yrs left)· nominal 20-yr term from priority
B01J 20/3293C01B 32/36B01J 20/28004C01B 32/336B01D 2253/304B01D 2253/25B01D 53/10B01J 20/324B01D 53/04B01J 20/3085C01B 32/342B01D 53/8665B01J 20/3208B01J 20/205B01J 20/20B01D 53/025B01D 2257/60B01J 20/3236B01J 20/3204B01D 2258/0283B01D 2257/602B01D 2253/102B01D 53/81B01D 53/64B01D 2253/202B01D 53/02B01J 20/22C01B 32/354
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Claims
Abstract
The present invention relates to sorbents including carbon and nitrogen. In various embodiments, the sorbent can remove mercury from a mercury-containing gas that includes sulfur(VI) such as SO 3 more efficiently than other sorbents. The sorbent can include a graphene edge comprising an active site for mercury oxidation and a nitrogen layer structure including cationic nitrogen atoms, neutral nitrogen atoms, or a combination thereof proximate the active site.
Claims
exact text as granted — not AI-modifiedWhat is claimed is:
1 . A nitrogen-containing activated carbon sorbent, comprising:
an activated carbon comprising nitrogen in a surface layer thereof, the activated carbon comprising a core comprising nitrogen, wherein the surface layer has a higher concentration of nitrogen than the core.
2 . The sorbent of claim 1 , wherein the surface layer of the sorbent comprises a layer at the surface of the sorbent having a thickness of about 0.001% to about 49% of the largest dimension of the sorbent.
3 . The sorbent of claim I, wherein the core of the sorbent comprises about 0.001 wt % to about 6 wt % nitrogen.
4 . The sorbent of claim 1 , wherein the surface layer of the sorbent comprises about 0.001 wt % to about 80 wt % nitrogen.
5 . The sorbent of claim 1 , wherein the surface layer comprises cationic nitrogen atoms, neutral nitrogen atoms, or a combination thereof.
6 . The sorbent of claim I, wherein the sorbent is a halogen- or halide-promoted activated carbon.
7 . The sorbent of claim 6 , wherein the halogen- or halide-promotion comprises promotion with HCl, HBr, HI, Br 2 , Cl 2 , I 2 , BrCl, IBr, ICl, ClF, PBr 3 , PCl 5 , SCl 2 , CuCl 2 , CuBr 2 , Al 2 Br 6 , FeI x (x=1, 2, 3, or 4), FeBr y (y=1, 2, 3, or 4), FeCl z (z=1, 2, 3, or 4), MnBr 2 , MnCl 2 , NiBr 2 , NiCl 2 , NiI 2 , ZnBr 2 , ZnCl 2 , ZnI 2 , NH 4 Br, NH 4 Cl, NH 4 I, NH 4 F, (NH 4 ) 2 SO 4 , H 2 SO 4 , NH 4 SO 4 H, (NH 4 ) 2 S 2 O 3 , FeNH 4 (SO 4 ) 2 , Fe(NH 4 ) 2 (SO 4 ) 2 , FeNH 4 Br 4 , FeNH 4 Cl 4 , AlNH 4 (SO 4 ) 2 , NaBr, NaCl, NaI, Br − , Cl − , I − , KI, KCl, LiCl, LiBr, AgCl, AgBr, CHI 3 , CH 3 Br, AuBr, MgBr 2 , MgCl 2 , CaI 2 , CaBr 2 , CaCl 2 , hydrates thereof, or a combination thereof.
8 . A method of making the sorbent of claim 1 , the method comprising:
contacting activated carbon with a nitrogen-containing compound to form the surface layer, to form the nitrogen-containing activated carbon sorbent of claim 1 .
9 . The method of claim 8 , wherein forming the surface layer comprises contacting the activated carbon with an ammonium salt, ammonium precursor, ammonium compound, an ammonium halide, a methylammonium halide, an ammonium salt of an oxyacid of a Group VI element, an ammonium salt of an oxyacid of a Group V element, or a combination thereof.
10 . The method of claim 9 , wherein the ammonium salt, ammonium precursor, or ammonium compound is ammonium bromide, ammonium iodide, ammonium chloride, an organic halide with a formula of CH 3 NH 3 X (wherein X is Cl, Br or I), ammonium sulfate, ammonium hydrogen sulfate, ammonium sulfite, ammonium hydrogen sulfite, ammonium persulfate, ammonium pyrosulfate, ammonium thiosulphate, ammonium dithionite, ammonium aluminium sulfate, ammonium iron sulfate, ammonium sulfamate, ammonium phosphate, diammonium phosphate, ammonium hydrogen phosphate, ammonium dihydrogen phosphate, ammonium thiophosate, ammonium nitrate, ammonium nitrite, ammonium carbonate, ammonium thiocyanate, ammonium sulfide, ammonium hydrogen sulfide, ammonium acetate, ammonium carbamate, ammonium carbonate, ammonium chlorate, ammonium chromate, ammonium fluoride, ammonium formate, ammonium hydroxide, ammonium perchlorate, sodium nitrite, sodium nitrate, lithium nitrite, lithium nitrate, barium nitrite, barium nitrate, cerium nitrite, cerium nitrate, FeNH 4 (SO 4 ) 2 , Fe(NH 4 ) 2 (SO 4 ) 2 , FeNH 4 Br 4 , FeNH 4 Cl 4 , AlNH 4 (SO 4 ) 2 , hydrates thereof, or a combination thereof.
11 . The method of claim 8 , comprising forming the surface layer in the mercury-containing gas.
12 . The method of claim 8 , comprising forming the surface layer comprises injecting the nitrogen-containing compound and the activated carbon in a flue gas in the same location or at different locations wherein:
the nitrogen-containing compound is deposited on the activated carbon to form the sorbent within the flue gas, the nitrogen-containing compound decomposes or vaporizes and then deposits on the activated carbon to form the sorbent, the nitrogen-containing compound deposits on the carbon to form the sorbent, or a combination thereof.
13 . The method of claim 8 , wherein the surface layer is formed on the sorbent prior to injecting the sorbent into a mercury-containing gas.
14 . The method of claim 8 , further comprising promoting the activated carbon comprising nitrogen in a surface layer thereof with a halogen- or halide-promoter.
15 . A method of making the sorbent of claim 1 , the method comprising promoting the activated carbon comprising nitrogen in a surface layer thereof with a halogen- or halide-promoter.
16 . The method of claim 15 , comprising performing the halogen- or halide-promotion in a mercury-containing gas
17 . The method of claim 16 , further comprising combusting coal comprising a halogen- or halide-containing material to form the mercury-containing gas.
18 . The method of claim 16 , further comprising adding the halogen- or halide-containing material to the coal.
19 . The method of claim 18 , wherein the halogen- or halide-containing material comprises HCl, HBr, HI, Br 2 , Cl 2 , I 2 , BrCl, IBr, ICl, ClF, PBr 3 , PCl 5 , SCl 2 , CuCl 2 , CuBr 2 , Al 2 Br 6 , FeI x (x=1, 2, 3, or 4), FeBr y (y=1, 2, 3, or 4), FeCl z (z=1, 2, 3, or 4), MnBr 2 , MnCl 2 , NiBr 2 , NiCl 2 , NiI 2 , ZnBr 2 , ZnCl 2 , ZnI 2 , NH 4 Br, NH 4 Cl, NH 4 I, NH 4 F, (NH 4 ) 2 SO 4 , H 2 SO 4 , NH 4 SO 4 H, (NH 4 ) 2 S 2 O 3 , FeNH 4 (SO 4 ) 2 , Fe(NH 4 ) 2 (SO 4 ) 2 , FeNH 4 Br 4 , FeNH 4 Cl 4 , AlNH 4 (SO 4 ) 2 , NaBr, NaCl, NaI, Br − , Cl − , I − , KI, KCl, LiCl, LiBr, AgCl, AgBr, CHI 3 , CH 3 Br, AuBr, MgBr 2 , MgCl 2 , CaI 2 , CaBr 2 , CaCl 2 , hydrates thereof, or a combination thereof.
20 . A method of using the sorbent of claim 1 to reduce the mercury content in a mercury-containing gas, the method comprising:
contacting the sorbent with the mercury-containing gas, to form a mercury-sorbent composition; and
separating at least some of the mercury-sorbent composition from the mercury-containing gas, to give a separated gas.Join the waitlist — get patent alerts
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