CN106268921A - 中高温scr分子筛脱硝催化剂及其制备方法 - Google Patents
中高温scr分子筛脱硝催化剂及其制备方法 Download PDFInfo
- Publication number
- CN106268921A CN106268921A CN201610581307.4A CN201610581307A CN106268921A CN 106268921 A CN106268921 A CN 106268921A CN 201610581307 A CN201610581307 A CN 201610581307A CN 106268921 A CN106268921 A CN 106268921A
- Authority
- CN
- China
- Prior art keywords
- molecular sieve
- high temperature
- denitrating catalyst
- tio
- preparation
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Pending
Links
- 239000002808 molecular sieve Substances 0.000 title claims abstract description 40
- URGAHOPLAPQHLN-UHFFFAOYSA-N sodium aluminosilicate Chemical compound [Na+].[Al+3].[O-][Si]([O-])=O.[O-][Si]([O-])=O URGAHOPLAPQHLN-UHFFFAOYSA-N 0.000 title claims abstract description 39
- 239000003054 catalyst Substances 0.000 title claims abstract description 28
- 238000002360 preparation method Methods 0.000 title claims abstract description 15
- 239000011248 coating agent Substances 0.000 claims abstract description 27
- 238000000576 coating method Methods 0.000 claims abstract description 27
- 229910052878 cordierite Inorganic materials 0.000 claims abstract description 21
- JSKIRARMQDRGJZ-UHFFFAOYSA-N dimagnesium dioxido-bis[(1-oxido-3-oxo-2,4,6,8,9-pentaoxa-1,3-disila-5,7-dialuminabicyclo[3.3.1]nonan-7-yl)oxy]silane Chemical compound [Mg++].[Mg++].[O-][Si]([O-])(O[Al]1O[Al]2O[Si](=O)O[Si]([O-])(O1)O2)O[Al]1O[Al]2O[Si](=O)O[Si]([O-])(O1)O2 JSKIRARMQDRGJZ-UHFFFAOYSA-N 0.000 claims abstract description 21
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N titanium dioxide Inorganic materials O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 claims abstract description 21
- 239000000919 ceramic Substances 0.000 claims abstract description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Chemical compound O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 38
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 claims description 31
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 claims description 25
- 239000008367 deionised water Substances 0.000 claims description 25
- 229910021641 deionized water Inorganic materials 0.000 claims description 25
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 claims description 24
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims description 20
- 238000003756 stirring Methods 0.000 claims description 16
- 229910021529 ammonia Inorganic materials 0.000 claims description 15
- 238000007598 dipping method Methods 0.000 claims description 15
- 239000007788 liquid Substances 0.000 claims description 13
- 229910001868 water Inorganic materials 0.000 claims description 13
- 229960000583 acetic acid Drugs 0.000 claims description 12
- 238000001035 drying Methods 0.000 claims description 12
- 239000012362 glacial acetic acid Substances 0.000 claims description 12
- XEEYBQQBJWHFJM-UHFFFAOYSA-N iron Substances [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 claims description 12
- FPCJKVGGYOAWIZ-UHFFFAOYSA-N butan-1-ol;titanium Chemical compound [Ti].CCCCO.CCCCO.CCCCO.CCCCO FPCJKVGGYOAWIZ-UHFFFAOYSA-N 0.000 claims description 11
- 239000012065 filter cake Substances 0.000 claims description 11
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 10
- 235000012239 silicon dioxide Nutrition 0.000 claims description 10
- 239000000377 silicon dioxide Substances 0.000 claims description 10
- 239000010949 copper Substances 0.000 claims description 9
- 229960000935 dehydrated alcohol Drugs 0.000 claims description 8
- 239000002253 acid Substances 0.000 claims description 7
- 238000000034 method Methods 0.000 claims description 7
- PAWQVTBBRAZDMG-UHFFFAOYSA-N 2-(3-bromo-2-fluorophenyl)acetic acid Chemical compound OC(=O)CC1=CC=CC(Br)=C1F PAWQVTBBRAZDMG-UHFFFAOYSA-N 0.000 claims description 6
- 238000000498 ball milling Methods 0.000 claims description 6
- 230000008569 process Effects 0.000 claims description 6
- OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 claims description 6
- XTVVROIMIGLXTD-UHFFFAOYSA-N copper(II) nitrate Chemical compound [Cu+2].[O-][N+]([O-])=O.[O-][N+]([O-])=O XTVVROIMIGLXTD-UHFFFAOYSA-N 0.000 claims description 4
- 229910052742 iron Inorganic materials 0.000 claims description 4
- -1 iron ion Chemical class 0.000 claims description 4
- JPVYNHNXODAKFH-UHFFFAOYSA-N Cu2+ Chemical compound [Cu+2] JPVYNHNXODAKFH-UHFFFAOYSA-N 0.000 claims description 3
- MVFCKEFYUDZOCX-UHFFFAOYSA-N iron(2+);dinitrate Chemical compound [Fe+2].[O-][N+]([O-])=O.[O-][N+]([O-])=O MVFCKEFYUDZOCX-UHFFFAOYSA-N 0.000 claims description 3
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 claims description 2
- 229910052802 copper Inorganic materials 0.000 claims description 2
- 229910001431 copper ion Inorganic materials 0.000 claims description 2
- 230000004048 modification Effects 0.000 claims description 2
- 238000012986 modification Methods 0.000 claims description 2
- 239000000047 product Substances 0.000 claims description 2
- 238000004140 cleaning Methods 0.000 claims 1
- DCKVNWZUADLDEH-UHFFFAOYSA-N sec-butyl acetate Chemical compound CCC(C)OC(C)=O DCKVNWZUADLDEH-UHFFFAOYSA-N 0.000 claims 1
- MWUXSHHQAYIFBG-UHFFFAOYSA-N nitrogen oxide Inorganic materials O=[N] MWUXSHHQAYIFBG-UHFFFAOYSA-N 0.000 abstract description 39
- 239000007789 gas Substances 0.000 abstract description 5
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 abstract description 4
- 229910052717 sulfur Inorganic materials 0.000 abstract description 4
- 239000011593 sulfur Substances 0.000 abstract description 4
- 238000012805 post-processing Methods 0.000 abstract description 2
- 239000000243 solution Substances 0.000 description 14
- 230000000694 effects Effects 0.000 description 5
- 238000005516 engineering process Methods 0.000 description 4
- 238000007873 sieving Methods 0.000 description 4
- 239000007864 aqueous solution Substances 0.000 description 3
- IDGUHHHQCWSQLU-UHFFFAOYSA-N ethanol;hydrate Chemical compound O.CCO IDGUHHHQCWSQLU-UHFFFAOYSA-N 0.000 description 3
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 2
- 238000002242 deionisation method Methods 0.000 description 2
- 239000003292 glue Substances 0.000 description 2
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 2
- VCJMYUPGQJHHFU-UHFFFAOYSA-N iron(3+);trinitrate Chemical compound [Fe+3].[O-][N+]([O-])=O.[O-][N+]([O-])=O.[O-][N+]([O-])=O VCJMYUPGQJHHFU-UHFFFAOYSA-N 0.000 description 2
- 230000003137 locomotive effect Effects 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- UGFAIRIUMAVXCW-UHFFFAOYSA-N Carbon monoxide Chemical compound [O+]#[C-] UGFAIRIUMAVXCW-UHFFFAOYSA-N 0.000 description 1
- 229910017827 Cu—Fe Inorganic materials 0.000 description 1
- GRYLNZFGIOXLOG-UHFFFAOYSA-N Nitric acid Chemical compound O[N+]([O-])=O GRYLNZFGIOXLOG-UHFFFAOYSA-N 0.000 description 1
- CBENFWSGALASAD-UHFFFAOYSA-N Ozone Chemical compound [O-][O+]=O CBENFWSGALASAD-UHFFFAOYSA-N 0.000 description 1
- 229910000831 Steel Inorganic materials 0.000 description 1
- 241000292525 Titanio Species 0.000 description 1
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 description 1
- 238000003916 acid precipitation Methods 0.000 description 1
- 230000009471 action Effects 0.000 description 1
- IWLUJCZGMDWKRT-UHFFFAOYSA-N azane oxygen(2-) titanium(4+) Chemical compound N.[O-2].[Ti+4].[O-2] IWLUJCZGMDWKRT-UHFFFAOYSA-N 0.000 description 1
- 239000004202 carbamide Substances 0.000 description 1
- 235000013877 carbamide Nutrition 0.000 description 1
- 238000010531 catalytic reduction reaction Methods 0.000 description 1
- 150000001768 cations Chemical class 0.000 description 1
- 230000008859 change Effects 0.000 description 1
- 239000003638 chemical reducing agent Substances 0.000 description 1
- 238000002485 combustion reaction Methods 0.000 description 1
- 238000011109 contamination Methods 0.000 description 1
- WXYNCCWBUXKSBG-UHFFFAOYSA-N copper;nitric acid Chemical compound [Cu].O[N+]([O-])=O WXYNCCWBUXKSBG-UHFFFAOYSA-N 0.000 description 1
- 238000004821 distillation Methods 0.000 description 1
- 239000003344 environmental pollutant Substances 0.000 description 1
- 238000003912 environmental pollution Methods 0.000 description 1
- 239000003546 flue gas Substances 0.000 description 1
- 239000002803 fossil fuel Substances 0.000 description 1
- 238000001879 gelation Methods 0.000 description 1
- 230000036541 health Effects 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 239000011259 mixed solution Substances 0.000 description 1
- 229910017604 nitric acid Inorganic materials 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 229910000069 nitrogen hydride Inorganic materials 0.000 description 1
- 231100000252 nontoxic Toxicity 0.000 description 1
- 230000003000 nontoxic effect Effects 0.000 description 1
- 239000003921 oil Substances 0.000 description 1
- 231100000719 pollutant Toxicity 0.000 description 1
- FGIUAXJPYTZDNR-UHFFFAOYSA-N potassium nitrate Chemical compound [K+].[O-][N+]([O-])=O FGIUAXJPYTZDNR-UHFFFAOYSA-N 0.000 description 1
- 238000000746 purification Methods 0.000 description 1
- 230000009257 reactivity Effects 0.000 description 1
- 230000009467 reduction Effects 0.000 description 1
- 238000006722 reduction reaction Methods 0.000 description 1
- 238000007670 refining Methods 0.000 description 1
- 239000010959 steel Substances 0.000 description 1
- 239000000758 substrate Substances 0.000 description 1
- 229910052720 vanadium Inorganic materials 0.000 description 1
- LEONUFNNVUYDNQ-UHFFFAOYSA-N vanadium atom Chemical compound [V] LEONUFNNVUYDNQ-UHFFFAOYSA-N 0.000 description 1
- 239000002912 waste gas Substances 0.000 description 1
Classifications
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J29/00—Catalysts comprising molecular sieves
- B01J29/04—Catalysts comprising molecular sieves having base-exchange properties, e.g. crystalline zeolites
- B01J29/06—Crystalline aluminosilicate zeolites; Isomorphous compounds thereof
- B01J29/08—Crystalline aluminosilicate zeolites; Isomorphous compounds thereof of the faujasite type, e.g. type X or Y
- B01J29/10—Crystalline aluminosilicate zeolites; Isomorphous compounds thereof of the faujasite type, e.g. type X or Y containing iron group metals, noble metals or copper
- B01J29/106—Y-type faujasite
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J29/00—Catalysts comprising molecular sieves
- B01J29/04—Catalysts comprising molecular sieves having base-exchange properties, e.g. crystalline zeolites
- B01J29/06—Crystalline aluminosilicate zeolites; Isomorphous compounds thereof
- B01J29/40—Crystalline aluminosilicate zeolites; Isomorphous compounds thereof of the pentasil type, e.g. types ZSM-5, ZSM-8 or ZSM-11, as exemplified by patent documents US3702886, GB1334243 and US3709979, respectively
- B01J29/42—Crystalline aluminosilicate zeolites; Isomorphous compounds thereof of the pentasil type, e.g. types ZSM-5, ZSM-8 or ZSM-11, as exemplified by patent documents US3702886, GB1334243 and US3709979, respectively containing iron group metals, noble metals or copper
- B01J29/46—Iron group metals or copper
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J29/00—Catalysts comprising molecular sieves
- B01J29/04—Catalysts comprising molecular sieves having base-exchange properties, e.g. crystalline zeolites
- B01J29/06—Crystalline aluminosilicate zeolites; Isomorphous compounds thereof
- B01J29/70—Crystalline aluminosilicate zeolites; Isomorphous compounds thereof of types characterised by their specific structure not provided for in groups B01J29/08 - B01J29/65
- B01J29/72—Crystalline aluminosilicate zeolites; Isomorphous compounds thereof of types characterised by their specific structure not provided for in groups B01J29/08 - B01J29/65 containing iron group metals, noble metals or copper
- B01J29/7215—Zeolite Beta
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J37/00—Processes, in general, for preparing catalysts; Processes, in general, for activation of catalysts
- B01J37/02—Impregnation, coating or precipitation
- B01J37/024—Multiple impregnation or coating
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J2229/00—Aspects of molecular sieve catalysts not covered by B01J29/00
- B01J2229/10—After treatment, characterised by the effect to be obtained
- B01J2229/18—After treatment, characterised by the effect to be obtained to introduce other elements into or onto the molecular sieve itself
Landscapes
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Crystallography & Structural Chemistry (AREA)
- Catalysts (AREA)
Abstract
本发明涉及一种中高温SCR分子筛脱硝催化剂及其制备方法,以蜂窝堇青石陶瓷块为载体,以TiO2为涂层,以改性分子筛为活性组分,其中,TiO2的含量为5‑15wt.%,改性分子筛的含量为5‑10wt.%。本发明对氮氧化物的脱除效率高,具有涂层牢固,稳定性高,且具有良好的抗硫能力,具有较强的抗机械振动的能力,不仅适用于固定源脱硝,也适合于机动车尾气后处理。
Description
技术领域
本发明涉及一种中高温SCR分子筛脱硝催化剂及其制备方法,属于脱硝催化剂领域。
背景技术
氮氧化物(NOx)是大气的主要污染物之一,其主要成分为一氧化氮(NO)和二氧化氮(NO2)。大量排放NOx能够引发光化学烟雾、酸雨、臭氧层空洞并产生温室效应。人类活动造成的NOx的排放是造成环境污染的主要来源,包括:来源于燃煤电厂、工业锅炉、化工厂和炼钢厂等固定源由于化石燃料燃烧和化学工业产生的废气;来源于汽油机车和柴油机车等移动源排放的尾气。随着经济的发展,人类活动造成的氮氧化物的排放呈现快速增长的趋势。尤其是近来频繁出现的雾霾,使大气污染成为了亟待解决的问题。
选择性催化还原氮氧化物(Selective Catalytic Reduction,SCR)是目前应用最广泛最成熟的脱硝技术。该技术是以氨类(液氨、尿素和氨水)为还原剂,在催化剂作用下将NOx还原为无污染的N2和H2O。但是,传统钒钛基脱硝催化剂具有反应活性温度窗口较窄(300-400℃),耐高温性能较差等特点,这限制了该类催化剂在柴油机和分布式能源站等产生的高温尾气中的使用。另外,由于含有V2O5,在以柴油车尾气为代表的移动源NOx净化过程中易发生升华或脱落,对生态环境和人体健康存在潜在危害。
针对现有的技术存在的问题,开发高温高效、性能稳定的SCR脱硝催化剂对减少柴油机和分布式能源站等高温脱硝领域的污染具有重要的现实意义。本发明适用于300-450℃中温和450-640℃高温控制固定源和移动源氮氧化物的排放,并且催化剂无毒,对环境友好。
发明内容
为解决上述现有技术存在的问题,本发明提供一种中高温SCR分子筛脱硝催化剂及其制备方法,对氮氧化物的脱除效率高,具有涂层牢固,稳定性高,且具有良好的抗硫能力,具有较强的抗机械振动的能力。
本发明所述的一种中高温SCR分子筛脱硝催化剂,以蜂窝堇青石陶瓷块为载体,以TiO2为涂层,以改性分子筛为活性组分,其中,TiO2的含量为5-15wt.%,改性分子筛的含量为5-10wt.%。
所述改性分子筛为通过铜离子和/或铁离子改性得到,其中铜或/和铁离子含量为1.5-2.5wt.%。
改性分子筛的制备方法包括如下步骤:
(1)将分子筛加入到硝酸铵溶液中,100-150℃下搅拌3-5h,过滤,所得滤饼用去离子水清洗并干燥,得到氨型分子筛;
(2)将氨型分子筛加入到硝酸铜或/和硝酸铁溶液中,60-80℃下搅拌1-2h,过滤,所得滤饼用去离子水清洗并干燥,随后400-600℃焙烧3-5h,得到改性分子筛。
所述分子筛为Y、β或ZSM-5中的一种。
所述的中高温SCR分子筛脱硝催化剂的制备方法,包括如下步骤:
(1)将蜂窝堇青石载体浸泡在HF酸溶液中1-2h进行预处理,去离子水清洗后烘干;
(2)将上述处理后堇青石浸渍在纳米TiO2溶胶中,浸渍5-10min后取出,吹尽孔道中残液,空气中阴干后,干燥,焙烧;
(3)将改性分子筛球磨后,与乙二醇、二氧化硅溶胶和去离子水按照(1-3):(0.5-3):(0.1-2):(0.5-3)混合,室温下搅拌3-5h,充分混合,制得涂覆浆液;
(4)将步骤(2)中得到的TiO2涂层堇青石载体浸渍在步骤(3)的涂覆浆液中,浸渍5-10min后取出,吹尽孔道中残液,空气中阴干后100-130℃干燥3-5h,随后400-600℃焙烧3-5h得到产品。
步骤(2)中,在100-130℃干燥3-5h,随后400-600℃焙烧3-5h。
所述纳米TiO2溶胶制备方法为:将钛酸丁酯与无水乙醇混合,并加入冰醋酸和水,制得纳米TiO2溶胶。
钛酸丁酯:无水乙醇:水:冰醋酸的摩尔比为1-2:20:8:9。
所述中高温为300-640℃。
为达到上述目的,本发明采用如下技术方案:
步骤1:将分子筛加入到0.5-1mol/L硝酸铵溶液中,100-150℃下搅拌3-5h,过滤,所得滤饼用去离子水清洗并干燥,得到氨型分子筛;将氨型分子筛加入到0.5-1mol/L硝酸铜或/和硝酸铁溶液中,60-100℃下搅拌1-2h,过滤,所得滤饼用去离子水清洗并干燥,随后400-600℃焙烧3-5h,得到改性分子筛。
步骤2:将蜂窝堇青石载体浸泡在0.05-0.1mol/L HF酸溶液中1-2h预处理,去离子水清洗后烘干;
步骤3:将钛酸丁酯与无水乙醇混合,并加入冰醋酸和水,其中钛酸丁酯:无水乙醇:水:冰醋酸的摩尔比为(0.5-2):(1-50):(1-10):(1-10),制得纳米TiO2溶胶;
步骤4:将上述处理后堇青石浸渍在纳米TiO2溶胶中,浸渍5-10min后取出,吹尽孔道中残液,空气中阴干后100-130℃干燥3-5h,随后400-600℃焙烧3-5h;
步骤5:将改性分子筛球磨后,与乙二醇、二氧化硅溶胶和去离子混合,改性分子筛:乙二醇:二氧化硅溶胶:去离子水的质量为比1-3:1.5:0.3:1.5。室温下搅拌3-5h,充分混合,制得涂覆浆液;
步骤6:将步骤4中得到的TiO2涂层堇青石载体浸渍在步骤5中的涂覆浆液中,浸渍5-10min后取出,吹尽孔道中残液,空气中阴干后100-130℃干燥3-5h,随后400-600℃焙烧3-5h。
本发明制备的催化剂在300-640℃范围内,对氮氧化物的脱除效率保持在90%以上,且具有良好的抗硫能力。
与现有技术相比,本发明具有以下有益效果:
本发明中高温SCR分子筛脱硝催化剂,对氮氧化物的脱除效率高,具有涂层牢固,稳定性高,且具有良好的抗硫能力,具有较强的抗机械振动的能力,不仅适用于固定源脱硝,也适合于机动车尾气后处理。
本发明催化剂在3000h-1的空速,450ppm NO+450ppm NH3+400ppm SO2+4%O2+12%CO2+8%H2O+N2的模拟烟气条件下,300-640℃的温度区间氮氧化物脱除效率保持在90%以上。
具体实施方式
下面结合实施例对本发明做进一步的说明。
实施例1
步骤1:将Y分子筛加入到1mol/L硝酸铵溶液中,110℃下搅拌3h,过滤,所得滤饼用去离子水清洗并干燥,得到氨型分子筛;将100g氨型分子筛加入到0.5mol/L硝酸铜溶液中,60℃下搅拌2h,过滤,所得滤饼用去离子水清洗并干燥,随后600℃焙烧3h,得到Cu改性分子筛。
步骤2:将200目蜂窝堇青石载体(40×40×100mm)浸泡在0.05mol/L HF酸溶液中1h预处理,去离子水清洗后110℃烘干;
步骤3:将20g钛酸丁酯与无水乙醇混合,并加入冰醋酸水溶液,其中,钛酸丁酯:无水乙醇:水:冰醋酸的摩尔比为1:20:8:9,制得纳米TiO2溶胶;
步骤4:将上述处理后堇青石浸渍在纳米TiO2溶胶中,浸渍5min后取出,吹尽孔道中残液,空气中阴干后100℃干燥3h,随后400℃焙烧5h;
步骤5:将Cu改性分子筛球磨后,过筛备用(D50<5μm)。取50g Cu改性分子筛与乙二醇、二氧化硅溶胶和去离子水按照一定比例混合,保证改性分子筛:乙二醇:二氧化硅溶胶:去离子水的质量为比1:1.5:0.3:1.5。室温下搅拌5h,保证充分混合,制得涂覆浆液;
步骤6:将步骤4中得到的TiO2涂层堇青石载体浸渍在步骤5中的涂覆浆液中,浸渍10min后取出,吹尽孔道中残液,空气中阴干后100℃干燥5h,随后400℃焙烧5h。
实施例2
步骤1:将商用β分子筛加入到1mol/L硝酸铵溶液中,130℃下搅拌4h,过滤,所得滤饼用去离子水清洗并干燥,得到氨型分子筛;将100g氨型分子筛加入到0.5mol/L硝酸铁溶液中,80℃下搅拌1h,过滤,所得滤饼用去离子水清洗并干燥,随后600℃焙烧3h,得到Fe改性分子筛。
步骤2:将200目蜂窝堇青石载体(40×40×100mm)浸泡在0.05mol/L HF酸溶液中2h预处理,去离子水清洗后110℃烘干;
步骤3:将20g钛酸丁酯与无水乙醇混合,并加入少量冰醋酸水溶液(钛酸丁酯:无水乙醇:水:冰醋酸的摩尔比为1.5:20:8:9),制得纳米TiO2溶胶;
步骤4:将上述处理后堇青石浸渍在纳米TiO2溶胶中,浸渍10min后取出,吹尽孔道中残液,空气中阴干后100℃干燥5h,随后550℃焙烧4h;
步骤5:将Fe改性分子筛球磨后,过筛备用(D50<5μm)。取50g Fe改性分子筛与乙二醇、二氧化硅溶胶和去离子水按照一定比例混合,保证改性分子筛:乙二醇:二氧化硅溶胶:去离子水的质量为比1.5:1.5:0.3:1.5。室温下搅拌4h,保证充分混合,制得涂覆浆液;
步骤6:将步骤4中得到的TiO2涂层堇青石载体浸渍在步骤5中的涂覆浆液中,浸渍8min后取出,吹尽孔道中残液,空气中阴干后110℃干燥5h,随后550℃焙烧4h。
实施例3
步骤1:将商用ZSM-5分子筛加入到1mol/L硝酸铵溶液中,150℃下搅拌5h,过滤,所得滤饼用去离子水清洗并干燥,得到氨型分子筛;将100g氨型分子筛加入到硝酸铜和硝酸铁混合溶液中(其中金属阳离子浓度为1mol/L,Cu2+:Fe3+=3:2),80℃下搅拌2h,过滤,所得滤饼用去离子水清洗并干燥,随后600℃焙烧3h,得到Cu&Fe改性分子筛。
步骤2:将200目蜂窝堇青石载体(40×40×100mm)浸泡在0.1mol/L HF酸溶液中2h预处理,去离子水清洗后110℃烘干;
步骤3:将20g钛酸丁酯与无水乙醇混合,并加入少量冰醋酸水溶液(钛酸丁酯:无水乙醇:水:冰醋酸的摩尔比为2:20:8:9),制得纳米TiO2溶胶;
步骤4:将上述处理后堇青石浸渍在纳米TiO2溶胶中,浸渍10min后取出,吹尽孔道中残液,空气中阴干后130℃干燥3h,随后600℃焙烧3h;
步骤5:将Cu&Fe改性分子筛球磨后,过筛备用,过筛备用(D50<5μm)。取50g Cu&Fe改性分子筛与乙二醇、二氧化硅溶胶和去离子水按照一定比例混合,保证改性分子筛:乙二醇:二氧化硅溶胶:去离子水的质量为比3:1.5:0.3:1.5。室温下搅拌3h,保证充分混合,制得涂覆浆液;
步骤6:将步骤4中得到的TiO2涂层堇青石载体浸渍在步骤5中的涂覆浆液中,浸渍5min后取出,吹尽孔道中残液,空气中阴干后130℃干燥3h,随后600℃焙烧3h。
表1为不同改性分子筛蜂窝涂覆催化剂活性组分的负载量。从表1分析数据可知:提高改性分子筛量、搅拌时间和涂覆时间在一定程度上可以提高分子筛在蜂窝载体上的上载量。
表1不同改性分子筛蜂窝涂覆催化剂活性组分的负载量
| 分子筛涂覆催化剂 | Cu/Y | Fe/β | Cu-Fe/ZSM-5 |
| 上载量/% | 6.35 | 9.04 | 15.39 |
Claims (9)
1.一种中高温SCR分子筛脱硝催化剂,其特征在于:以蜂窝堇青石陶瓷块为载体,以TiO2为涂层,以改性分子筛为活性组分,其中,TiO2的含量为5-15wt.%,改性分子筛的含量为5-10wt.%。
2.根据权利要求1所述的中高温SCR分子筛脱硝催化剂,其特征在于:所述改性分子筛为通过铜离子和/或铁离子改性得到,其中改性分子筛中铜或/和铁离子含量为1.5-2.5wt.%。
3.根据权利要求1所述的中高温SCR分子筛脱硝催化剂,其特征在于:改性分子筛的制备方法包括如下步骤:
(1)将分子筛加入到硝酸铵溶液中,100-150℃下搅拌3-5h,过滤,所得滤饼用去离子水清洗并干燥,得到氨型分子筛;
(2)将氨型分子筛加入到硝酸铜或硝酸铁溶液中,60-80℃下搅拌1-2h,过滤,所得滤饼用去离子水清洗并干燥,随后400-600℃焙烧3-5h,得到改性分子筛。
4.根据权利要求3所述中高温SCR分子筛脱硝催化剂,其特征在于:所述分子筛为Y、β或ZSM-5中的一种。
5.一种权利要求1所述的中高温SCR分子筛脱硝催化剂的制备方法,其特征在于:包括如下步骤:
(1)将蜂窝堇青石载体浸泡在HF酸溶液中1-2h进行预处理,去离子水清洗后烘干;
(2)将上述处理后堇青石浸渍在纳米TiO2溶胶中,浸渍5-10min后取出,吹尽孔道中残液,空气中阴干后,干燥,焙烧;
(3)将改性分子筛球磨后,与乙二醇、二氧化硅溶胶和去离子水按照(1-3):(0.5-2):(0.1-0.5):(0.5-5)混合,室温下搅拌3-5h,充分混合,制得涂覆浆液;
(4)将步骤(2)中得到的TiO2涂层堇青石载体浸渍在步骤(3)的涂覆浆液中,浸渍5-10min后取出,吹尽孔道中残液,空气中阴干后100-130℃干燥3-5h,随后400-600℃焙烧3-5h得到产品。
6.根据权利要求5所述的中高温SCR分子筛脱硝催化剂的制备方法,其特征在于:步骤(2)中,在100-130℃干燥3-5h,随后400-600℃焙烧3-5h。
7.根据权利要求5所述的中高温SCR分子筛脱硝催化剂的制备方法,其特征在于:所述纳米TiO2溶胶制备方法为:将钛酸丁酯与无水乙醇混合,并加入冰醋酸和水,制得纳米TiO2溶胶。
8.根据权利要求7所述的中高温SCR分子筛脱硝催化剂的制备方法,其特征在于:钛酸丁酯:无水乙醇:水:冰醋酸的摩尔比为1-5:5-30:1-10:5-10。
9.根据权利要求5所述的中高温SCR分子筛脱硝催化剂的制备方法,其特征在于:所述的中高温为300-640℃。
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN201610581307.4A CN106268921A (zh) | 2016-07-21 | 2016-07-21 | 中高温scr分子筛脱硝催化剂及其制备方法 |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN201610581307.4A CN106268921A (zh) | 2016-07-21 | 2016-07-21 | 中高温scr分子筛脱硝催化剂及其制备方法 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CN106268921A true CN106268921A (zh) | 2017-01-04 |
Family
ID=57652023
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CN201610581307.4A Pending CN106268921A (zh) | 2016-07-21 | 2016-07-21 | 中高温scr分子筛脱硝催化剂及其制备方法 |
Country Status (1)
| Country | Link |
|---|---|
| CN (1) | CN106268921A (zh) |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN110508318A (zh) * | 2019-10-22 | 2019-11-29 | 山东国瓷功能材料股份有限公司 | 一种复合脱硝催化剂及其制备方法和应用 |
| CN115487857A (zh) * | 2022-09-15 | 2022-12-20 | 启源(西安)大荣环保科技有限公司 | 一种钇改性氧化钛为载体的高温脱硝催化剂及制备方法 |
Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN102762827A (zh) * | 2010-04-14 | 2012-10-31 | 尤米科尔股份公司及两合公司 | 具有改进特征的还原催化剂涂覆的柴油颗粒过滤器 |
| CN104353485A (zh) * | 2014-11-06 | 2015-02-18 | 清华大学 | 分子筛脱硝的蜂窝载体催化剂制备方法 |
| CN105473230A (zh) * | 2013-08-14 | 2016-04-06 | 迪耐斯公司 | 涂覆的颗粒过滤器 |
-
2016
- 2016-07-21 CN CN201610581307.4A patent/CN106268921A/zh active Pending
Patent Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN102762827A (zh) * | 2010-04-14 | 2012-10-31 | 尤米科尔股份公司及两合公司 | 具有改进特征的还原催化剂涂覆的柴油颗粒过滤器 |
| CN105473230A (zh) * | 2013-08-14 | 2016-04-06 | 迪耐斯公司 | 涂覆的颗粒过滤器 |
| CN104353485A (zh) * | 2014-11-06 | 2015-02-18 | 清华大学 | 分子筛脱硝的蜂窝载体催化剂制备方法 |
Non-Patent Citations (1)
| Title |
|---|
| 沈岳松等: "整装脱硝催化剂载体介孔TiO2涂层的制备", 《材料工程》 * |
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN110508318A (zh) * | 2019-10-22 | 2019-11-29 | 山东国瓷功能材料股份有限公司 | 一种复合脱硝催化剂及其制备方法和应用 |
| CN115487857A (zh) * | 2022-09-15 | 2022-12-20 | 启源(西安)大荣环保科技有限公司 | 一种钇改性氧化钛为载体的高温脱硝催化剂及制备方法 |
| CN115487857B (zh) * | 2022-09-15 | 2024-07-09 | 启源(西安)大荣环保科技有限公司 | 一种钇改性氧化钛为载体的高温脱硝催化剂及制备方法 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| US20190224663A1 (en) | Preparation Method of Denitration Catalyst with Wide Operating Temperature Range for Flue Gas | |
| CN110354677B (zh) | 一种烧结、球团机头烟气排放净化系统 | |
| CN111036280B (zh) | Fe/Cu-SSZ-13分子筛的制备方法 | |
| CN103157505A (zh) | 一种Cu-SSZ-13催化剂、制备方法及其用途 | |
| JPH02194819A (ja) | 酸素含有排ガス中に存在する窒素酸化物の還元方法 | |
| CN102029178A (zh) | 铜基分子筛催化剂及其制备方法 | |
| CN105107514A (zh) | 一种蜂窝状非钒脱硝成型催化剂、制备方法及其用途 | |
| CN112657541B (zh) | 一种分子筛基低温环保型scr脱硝催化剂的制备方法 | |
| CN107282141B (zh) | 一种用于舰船烟气脱硫脱硝的光催化剂及其制备方法 | |
| CN103816799A (zh) | 提高sncr脱硝效率的脱硝剂及其制备方法 | |
| CN108993476B (zh) | 金属氧化物-钒酸盐/TiO2催化剂及其制备方法和应用 | |
| WO2015158139A1 (zh) | 一种有效抑制so2氧化的脱硝催化剂的制备方法 | |
| CN102626653A (zh) | 用于氨选择性催化消除NOx的SAPO-18负载Cu-Fe催化剂的制备方法 | |
| CN102553572A (zh) | 一种宽活性温度窗口的scr催化剂及其制备方法 | |
| CN103566964A (zh) | 一种低温催化剂及其制备方法 | |
| CN107485997A (zh) | 一种烟气多污染物协同脱除系统及方法 | |
| CN110694670A (zh) | 一种柴油车尾气净化分子筛的制备方法 | |
| CN102188889B (zh) | 联合脱除烟气中二氧化硫、氮氧化物和汞的装置及方法 | |
| CN106268921A (zh) | 中高温scr分子筛脱硝催化剂及其制备方法 | |
| CN110947416B (zh) | 用于nh3-scr的铁/分子筛催化剂及其制备方法和应用 | |
| CN109985663B (zh) | 一种对一锅法原位合成的Cu-SSZ-13分子筛进行后处理的方法 | |
| CN104415745A (zh) | 一种钙钛矿结构物质及其制备方法 | |
| CN109894108A (zh) | 一种低温高效scr脱硝催化剂 | |
| CN104475152B (zh) | 用于氮氧化物氢气选择催化还原的催化剂及其应用 | |
| CN104415747A (zh) | 一种钛钨粉及其制备方法 |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| C06 | Publication | ||
| PB01 | Publication | ||
| C10 | Entry into substantive examination | ||
| SE01 | Entry into force of request for substantive examination | ||
| RJ01 | Rejection of invention patent application after publication |
Application publication date: 20170104 |
|
| RJ01 | Rejection of invention patent application after publication |