CN109225248B - 蜂窝式低温脱硝催化剂及其制备工艺 - Google Patents
蜂窝式低温脱硝催化剂及其制备工艺 Download PDFInfo
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- 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 description 1
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- WPBNNNQJVZRUHP-UHFFFAOYSA-L manganese(2+);methyl n-[[2-(methoxycarbonylcarbamothioylamino)phenyl]carbamothioyl]carbamate;n-[2-(sulfidocarbothioylamino)ethyl]carbamodithioate Chemical compound [Mn+2].[S-]C(=S)NCCNC([S-])=S.COC(=O)NC(=S)NC1=CC=CC=C1NC(=S)NC(=O)OC WPBNNNQJVZRUHP-UHFFFAOYSA-L 0.000 description 1
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- B01D53/00—Separation of gases or vapours; Recovering vapours of volatile solvents from gases; Chemical or biological purification of waste gases, e.g. engine exhaust gases, smoke, fumes, flue gases, aerosols
- B01D53/34—Chemical or biological purification of waste gases
- B01D53/74—General processes for purification of waste gases; Apparatus or devices specially adapted therefor
- B01D53/86—Catalytic processes
- B01D53/8621—Removing nitrogen compounds
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- B01D53/8628—Processes characterised by a specific catalyst
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- B01J23/84—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of the iron group metals or copper combined with metals, oxides or hydroxides provided for in groups B01J23/02 - B01J23/36 with arsenic, antimony, bismuth, vanadium, niobium, tantalum, polonium, chromium, molybdenum, tungsten, manganese, technetium or rhenium
- B01J23/889—Manganese, technetium or rhenium
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Abstract
本发明公开了一种蜂窝式低温脱硝催化剂及其制备工艺,本发明催化剂的制备工艺简单,易于成型,且制备的催化剂低温活性高,抗水抗硫抗碱(土)金属中毒能力强,且本发明以废SCR催化剂为原料,成本低廉,可实现资源化利用废SCR催化剂,可实现废SCR催化剂的循环利用。
Description
技术领域
本发明涉及一种蜂窝式低温脱硝催化剂及其制备工艺。
背景技术
在氮氧化物污染控制领域中,选择性催化还原法(SCR,selective catalyticreduction)是应用最为广泛的烟气脱硝技术。SCR脱硝催化剂以NH3作为还原剂,借助催化效应,将烟气中有害的氮氧化合物还原成无害的氮气。目前,低温脱硝催化剂已经成为SCR催化剂领域的一个热门研究课题。
目前研究的低温SCR催化剂的活性组分以过渡金属为主,Mn元素因具有多种价态,且价态之间转变所需要的活化能较低,在低温下具有优异的脱硝性能,是公认的低温脱硝催化剂活性组分,但是其抗水抗硫性差,并且在生产过程中不管是用硝酸锰还是氢氧化锰,都会由于分解温度低(200℃)导致生产的产品出现炸裂,机械强度差,导致成型蜂窝困难,生产成本高。
专利CN 201610056551.9公开了一种蜂窝整体式低温脱硝催化剂及其制备工艺,其将过渡金属(铁、钴、铜、镍、锰、铈)盐浸入钛白粉中,形成悬浊液,然后和其它助剂配成浆料,涂覆在蜂窝堇青石载体上,然后干燥煅烧得到蜂窝整体式低温脱硝催化剂,但该低温脱硝催化剂在低温高尘烟气中活性组分容易磨损,难以工业化应用,并且催化剂的制备工艺复杂,成本较高。
专利CN 201611002394.X公开了一种蜂窝状Mn基低温脱硝催化剂的制备工艺,其将载体和活性组分锰、铈和铁盐煅烧形成粉末状物料,然后挤出成型得到锰基蜂窝状低温脱硝催化剂,但该低温脱硝催化剂的抗硫性差,也没有考察水对催化剂的影响,容易失活。
专利201711195037.4公开了一种抗碱中毒铜基尖晶石低温脱硝催化剂的制备工艺,其将铜盐和金属盐、金属盐、蒸馏水和混酸溶液形成溶液,然后干燥,在富氧气氛条件下,煅烧得到抗碱中毒铜基尖晶石低温脱硝催化剂,但该低温脱硝催化剂为粉末样品,没有成型,并且也没有考察水对催化剂影响,难以工业化应用。
可见,需要研发一种具有抗水抗硫抗碱(土)金属中毒能力强的蜂窝式低温脱硝催化剂。
发明内容
本发明的目的在于提供一种蜂窝式低温脱硝催化剂及其制备工艺,本发明催化剂的制备工艺简单,易于成型,且制备的催化剂低温活性高,抗水抗硫抗碱(土)金属中毒能力强,且本发明以废SCR催化剂为原料,成本低廉,可实现资源化利用废SCR催化剂,可实现废SCR催化剂的循环利用。
为实现上述目的,本发明提供一种蜂窝式低温脱硝催化剂的制备工艺,包括如下步骤:
1)将经过清洗干燥的废SCR催化剂研磨后,投入配有钴盐、铈盐和锰盐的水溶液中,在80~100℃打浆,加入碳酸铵生成沉淀,老化4~6h,过滤沉淀并清洗干燥;
2)将步骤1)所得沉淀与拟薄水铝石、硅溶胶、羟甲基纤维素、石墨以及去离子水混炼成塑性泥料;
3)对步骤2)所得塑性泥料进行过滤杂质、练泥,陈腐;
4)将步骤3)所得泥料真空挤出成型,得到蜂窝状湿坯;
5)将步骤4)所得蜂窝状湿坯干燥后浸入氟碳树脂乳液,取出后进行再次干燥,然后煅烧成蜂窝式低温脱硝催化剂。
优选的,步骤1)中,钴盐选自硝酸钴、草酸钴、醋酸钴中的一种;铈盐选自硝酸铈、硝酸铈、醋酸铈中的一种;锰盐选自硝酸锰、醋酸锰、草酸锰中的一种。
优选的,步骤5)中,氟碳树脂乳液中的氟碳树脂选自聚四氟乙烯、聚三氟氯乙烯、聚氟乙烯树脂中的一种。
优选的,上述蜂窝式低温脱硝催化剂的制备工艺,包括如下步骤:
1)将100重量份经过清洗干燥后的废SCR催化剂研磨至粒度d50为3~5μm,然后投入配有2~6重量份钴盐、9~50重量份铈盐、25~70重量份锰盐的350~500重量份水溶液中,在80~100℃打浆30~60min,加入20~60重量份碳酸铵生成沉淀,老化4~6h,过滤沉淀并用去离子水清洗2~4次,在90~110℃干燥2~4h;
2)将步骤1)所得沉淀与0.8~1.5重量份拟薄水铝石、3~5重量份硅溶胶、0.8~1.2重量份羟甲基纤维素、0.5~0.8重量份石墨以及80~200重量份去离子水混炼成塑性泥料;
3)对步骤2)所得塑性泥料进行过滤杂质、练泥,陈腐;
4)将步骤3)所得泥料真空挤出成型,得到蜂窝状湿坯;
5)将步骤4)所得蜂窝状湿坯干燥后浸入氟碳树脂乳液,取出后进行于80~100℃再次干燥6~8h,然后于350~450℃煅烧6~8h,制成蜂窝式低温脱硝催化剂。
优选的,步骤5)中,氟碳树脂乳液中氟碳树脂的质量浓度为0.1%~0.3%。
本发明还提供上述制备工艺所制得的蜂窝式低温脱硝催化剂。
本发明的优点和有益效果在于:提供一种蜂窝式低温脱硝催化剂及其制备工艺,本发明催化剂的制备工艺简单,易于成型,且制备的催化剂低温活性高,抗水抗硫抗碱(土)金属中毒能力强,且本发明以废SCR催化剂为原料,成本低廉,可实现资源化利用废SCR催化剂,可实现废SCR催化剂的循环利用。
本发明将钴盐、锰盐和铈盐沉淀成为碳酸盐,碳酸盐分解成为氧化物的温度高,可缓慢释放气体,不会出现蜂窝催化剂炸裂、机械强度差的问题,活性组分前驱体、载体与沉淀剂一起沉淀,活性组分与载体交互在一起,使得活性组分的分散性更好,更稳定,低温脱硝活性高。
本发明将催化剂浸泡在氟炭树脂中,可使氟炭树脂渗入催化剂的内外壁中,填充催化剂内外壁壁面细微孔隙,形成致密的孔壁渗透层膜,高温氟可与过渡金属反应生成表面氟化氧化物,使催化剂具有抗水抗硫能力,并且增加催化剂强度,使催化剂具有高强度和抗碱(土)金属能力。
本发明可采用清洗彻底干燥的废SCR催化剂作为载体,来源丰富,成本低廉,可资源化利用废SCR催化剂,实现了废SCR催化剂循环利用。本发明催化剂的制备时间短,为工业化实际应用打下了基础。
具体实施方式
下面结合实施例,对本发明的具体实施方式作进一步描述。以下实施例仅用于更加清楚地说明本发明的技术方案,而不能以此来限制本发明的保护范围。
本发明具体实施的技术方案是:
实施例1
1)将100重量份经过清洗干燥后的废SCR催化剂研磨至粒度d50为3~5μm,然后投入配有4.35重量份硝酸钴、9.1重量份硝酸铈、69重量份硝酸锰的350重量份水溶液中,在80℃打浆60min,加入22.8重量份碳酸铵生成沉淀,老化4h,过滤沉淀并用去离子水清洗2次,在90℃干燥4h;
2)将步骤1)所得沉淀与0.8重量份拟薄水铝石、3重量份硅溶胶、0.8重量份羟甲基纤维素、0.5重量份石墨以及80重量份去离子水混炼成塑性泥料;
3)对步骤2)所得塑性泥料进行过滤杂质、练泥,陈腐;
4)将步骤3)所得泥料真空挤出成型,得到蜂窝状湿坯;
5)将步骤4)所得蜂窝状湿坯干燥后浸入氟碳树脂乳液(氟碳树脂乳液中氟碳树脂的质量浓度为0.1%),取出后进行于80℃再次干燥8h,然后于350℃煅烧8h,制成蜂窝式低温脱硝催化剂。
实施例2
1)将100重量份经过清洗干燥后的废SCR催化剂研磨至粒度d50为3~5μm,然后投入配有5.43重量份草酸钴、45.2重量份草酸铈、44.12重量份草酸锰的500重量份水溶液中,在100℃打浆30min,加入55.52重量份碳酸铵生成沉淀,老化6h,过滤沉淀并用去离子水清洗4次,在110℃干燥2h;
2)将步骤1)所得沉淀与1.5重量份拟薄水铝石、5重量份硅溶胶、1.2重量份羟甲基纤维素、0.8重量份石墨以及100重量份去离子水混炼成塑性泥料;
3)对步骤2)所得塑性泥料进行过滤杂质、练泥,陈腐;
4)将步骤3)所得泥料真空挤出成型,得到蜂窝状湿坯;
5)将步骤4)所得蜂窝状湿坯干燥后浸入氟碳树脂乳液(氟碳树脂乳液中氟碳树脂的质量浓度为0.3%),取出后进行于100℃再次干燥6h,然后于450℃煅烧6h,制成蜂窝式低温脱硝催化剂。
实施例3
1)将100重量份经过清洗干燥后的废SCR催化剂研磨至粒度d50为3~5μm,然后投入配有5.07重量份醋酸钴、42.2重量份醋酸铈、27.5重量份醋酸锰的400重量份水溶液中,在90℃打浆45min,加入56.2重量份碳酸铵生成沉淀,老化5h,过滤沉淀并用去离子水清洗3次,在100℃干燥3h;
2)将步骤1)所得沉淀与1重量份拟薄水铝石、4重量份硅溶胶、1重量份羟甲基纤维素、0.7重量份石墨以及90重量份去离子水混炼成塑性泥料;
3)对步骤2)所得塑性泥料进行过滤杂质、练泥,陈腐;
4)将步骤3)所得泥料真空挤出成型,得到蜂窝状湿坯;
5)将步骤4)所得蜂窝状湿坯干燥后浸入氟碳树脂乳液(氟碳树脂乳液中氟碳树脂的质量浓度为0.2%),取出后进行于80℃再次干燥8h,然后于350℃煅烧8h,制成蜂窝式低温脱硝催化剂。
实施例4
1)将100重量份经过清洗干燥后的废SCR催化剂研磨至粒度d50为3~5μm,然后投入配有2.89重量份硝酸钴、12.05重量份草酸铈、39.1重量份醋酸锰的450重量份水溶液中,在100℃打浆45min,加入24.95重量份碳酸铵生成沉淀,老化5h,过滤沉淀并用去离子水清洗2次,在90℃干燥4h;
2)将步骤1)所得沉淀与0.8重量份拟薄水铝石、3重量份硅溶胶、0.8重量份羟甲基纤维素、0.5重量份石墨以及200重量份去离子水混炼成塑性泥料;
3)对步骤2)所得塑性泥料进行过滤杂质、练泥,陈腐;
4)将步骤3)所得泥料真空挤出成型,得到蜂窝状湿坯;
5)将步骤4)所得蜂窝状湿坯干燥后浸入氟碳树脂乳液(氟碳树脂乳液中氟碳树脂的质量浓度为0.3%),取出后进行于80℃再次干燥8h,然后于400℃煅烧8h,制成蜂窝式低温脱硝催化剂。
实施例5
1)将100重量份经过清洗干燥后的废SCR催化剂研磨至粒度d50为3~5μm,然后投入配有4.76重量份硝酸钴、19.8重量份醋酸铈、25.77重量份醋酸锰的500重量份水溶液中,在100℃打浆60min,加入32.65重量份碳酸铵生成沉淀,老化4h,过滤沉淀并用去离子水清洗2次,在90℃干燥4h;
2)将步骤1)所得沉淀与0.8重量份拟薄水铝石、3重量份硅溶胶、0.8重量份羟甲基纤维素、0.5重量份石墨以及200重量份去离子水混炼成塑性泥料;
3)对步骤2)所得塑性泥料进行过滤杂质、练泥,陈腐;
4)将步骤3)所得泥料真空挤出成型,得到蜂窝状湿坯;
5)将步骤4)所得蜂窝状湿坯干燥后浸入氟碳树脂乳液(氟碳树脂乳液中氟碳树脂的质量浓度为0.25%),取出后进行于80℃再次干燥8h,然后于350℃煅烧8h,制成蜂窝式低温脱硝催化剂。
脱硝实验
准备三个实验样品:
样品1:实施例1制得的脱硝催化剂,作为新鲜催化剂;
样品2:在实施例1制得的脱硝催化剂上负载1.0wt%的K2O,进行钾中毒实验;
样品3:在实施例1制得的脱硝催化剂上负载2.5wt%的CaO,进行钙中毒实验;
然后用烟气分析仪检测各样品的脱硝效率;测试条件为:NO 500ppm,NH3500ppm,O210%,SO2500ppm,10%H2O,N2为平衡气,空速5000h-1,检测温度150~250℃,催化剂20×20孔,长度500mm。检测结果如表1所示。
表1 催化剂脱硝效率检测结果
从表1可以看出,本发明脱硝催化剂的低温活性高,在高硫高水条件下的脱硝效率比较高,并且负载碱金属钾及碱土金属钙后的脱硝效率也比较高。可见,本发明蜂窝式低温脱硝催化剂的抗水抗硫抗碱(土)金属中毒能力比较强。
以上所述仅是本发明的优选实施方式,应当指出,对于本技术领域的普通技术人员来说,在不脱离本发明技术原理的前提下,还可以做出若干改进和润饰,这些改进和润饰也应视为本发明的保护范围。
Claims (1)
1.蜂窝式低温脱硝催化剂的制备工艺,其特征在于,包括如下步骤:
1)将100重量份经过清洗干燥后的废SCR催化剂研磨至粒度d50为3~5μm,然后投入配有2~6重量份钴盐、9~50重量份铈盐、25~70重量份锰盐的350~500重量份水溶液中,在80~100℃打浆30~60min,加入20~60重量份碳酸铵生成沉淀,老化4~6h,过滤沉淀并用去离子水清洗2~4次,在90~110℃干燥2~4h;钴盐选自硝酸钴、草酸钴、醋酸钴中的一种;铈盐选自硝酸铈、草酸铈、醋酸铈中的一种;锰盐选自硝酸锰、醋酸锰、草酸锰中的一种;
2)将步骤1)所得沉淀与0.8~1.5重量份拟薄水铝石、3~5重量份硅溶胶、0.8~1.2重量份羟甲基纤维素、0.5~0.8重量份石墨以及80~200重量份去离子水混炼成塑性泥料;
3)对步骤2)所得塑性泥料进行过滤杂质、练泥,陈腐;
4)将步骤3)所得泥料真空挤出成型,得到蜂窝状湿坯;
5)将步骤4)所得蜂窝状湿坯干燥后浸入氟碳树脂乳液,取出后于80~100℃再次干燥6~8h,然后于350~450℃煅烧6~8h,制成蜂窝式低温脱硝催化剂;氟碳树脂乳液中的氟碳树脂选自聚四氟乙烯、聚三氟氯乙烯、聚氟乙烯树脂中的一种;氟碳树脂乳液中氟碳树脂的质量浓度为0.1%~0.3%。
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