Process for production of sulfuric acid
US-2018127271-A1 · May 10, 2018 · US
US2016236145A1 · US · A1
| Field | Value |
|---|---|
| Publication number | US-2016236145-A1 |
| Application number | US-201514888112-A |
| Country | US |
| Kind code | A1 |
| Filing date | Jun 17, 2015 |
| Priority date | Nov 7, 2014 |
| Publication date | Aug 18, 2016 |
| Grant date | — |
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The present invention provides a flue gas treatment method and a denitration and SO 3 reduction apparatus configured to efficiently reduce the concentration of SO 3 in a combustion flue gas and also efficiently reduce NO x in the combustion flue gas at treatment costs lower than those of conventional methods. The flue gas treatment method performs a treatment for reducing SO 3 into SO 2 by adding a compound including the elements H and C to a combustion flue gas including SO 3 as well as NO x in an oxygen atmosphere as a first additive, and then by bringing the combustion flue gas into contact with a catalyst including an oxide constituted by one or more of elements selected from the group consisting of Ti, Si, Zr, and Ce and/or a mixed oxide and/or a complex oxide including two or more of the elements selected from the group as a carrier.
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1 . A flue gas treatment method comprising the steps of: adding a 3C-5C olefinic hydrocarbon (unsaturated hydrocarbon) to a combustion flue gas including SO 3 as well as NO x as a first additive; and then, bringing the combustion flue gas into contact with a catalyst which includes an oxide constituted by one or more of elements selected from the group consisting of Ti, Si, Zr, and Ce and/or a mixed oxide and/or a complex oxide constituted by two or more of elements selected from the group as a carrier and which does not include a noble metal, and thereby SO 3 is treated by reduction into SO 2 . 2 . The flue gas treatment method according to claim 1 , wherein the 3C-5C olefinic hydrocarbon (unsaturated hydrocarbon) is one or more selected from the group consisting of C 3 H 6 , C 4 H 8 , and C 5 H 10 . 3 . The flue gas treatment method according to claim 2 , wherein the C 4 H 8 and C 5 H 10 are a geometric isomer or a racemic body of either one of them. 4 . The flue gas treatment method according to claim 1 , wherein the carrier includes a mixed oxide and/or a complex oxide including one or more selected from the group consisting of TiO 2 —SiO 2 , TiO 2 —ZrO 2 , and TiO 2 —CeO 2 . 5 . The flue gas treatment method according to 4 claim 1 , wherein the catalyst is a catalyst in which a metal oxide including one or more selected from the group consisting of V 2 O 5 , WO 3 , MoO 3 , Mn 2 O 3 , MnO 2 , NiO, and Co 3 O 4 is carried on the complex oxide as the carrier. 6 . The flue gas treatment method according to claim 5 , wherein a metallosilicate-base complex oxide, in which at least a part of Al and/or Si in a zeolite crystal structure is substituted with one or more selected from the group consisting of Ti, V, Mn, Fe, and Co, is coated onto the catalyst. 7 . The flue gas treatment method according to claim 1 , wherein a treatment for reducing SO 3 into SO 2 is performed in a temperature range of 250° C. to 450° C. 8 . The flue gas treatment method according to claim 7 , wherein a treatment for reducing SO 3 into SO 2 is performed in a temperature range of 300° C. to 400° C. 9 . An SO 3 reduction apparatus comprising: a first injection device configured to obtain add a first additive to a combustion flue gas containing SO 3 as well as NO x ; and a catalyst layer including a catalyst through which the combustion flue gas is allowed to flow, wherein the first additive is a 3 C- 5 C olefinic hydrocarbon (unsaturated hydrocarbon), wherein the catalyst does not include a noble metal and includes an oxide including one or more of elements selected from the group consisting of Ti, Si, Zr, and Ce and/or a mixed oxide and/or a complex oxide including two or more of elements selected from the group as a carrier, and wherein the SO 3 reduction apparatus is configured to perform a treatment for reducing SO 3 to SO 2 . 10 . The SO 3 reduction apparatus according to claim 9 , wherein the 3C-5C olefinic hydrocarbon (unsaturated hydrocarbon) is one or more selected from the group consisting of C 3 H 6 , C 4 H 8 , and C 5 H 10 . 11 . The SO 3 reduction apparatus according to claim 10 , wherein the C 4 H 8 and C 5 H 10 are a geometric isomer or a racemic body of either one thereof. 12 . The SO 3 reduction apparatus according to claim 9 , wherein the carrier includes a mixed oxide and/or a complex oxide including one or more selected from the group consisting of TiO 2 —SiO 2 , TiO 2 —ZrO 2 , and TiO 2 —CeO 2 . 13 . The SO 3 reduction apparatus according to claim 9 , wherein the catalyst is a catalyst in which a metal oxide including one or more selected from the group consisting of V 2 O 5 , WO 3 , MoO 3 , Mn 2 O 3 , MnO 2 , NiO, and Co 3 O 4 is carried on the complex oxide as the carrier. 14 . The SO 3 reduction apparatus according to claim 9 , wherein the catalyst layer includes: a first catalyst layer arranged on a back stream side of the first injection device and configured to reduce the concentration of SO 3 ; and a second catalyst layer arranged on a back stream side of a second injection device arranged close to the first injection device and configured to add NH 3 to the combustion flue gas as a second additive, the second catalyst layer being configured to perform denitration, and wherein the first catalyst layer is arranged on a front stream side or a back stream side of the second catalyst layer.
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