CN106984331B - 一种Pd-Cu-Sn/凹凸棒土催化剂及其制备方法 - Google Patents
一种Pd-Cu-Sn/凹凸棒土催化剂及其制备方法 Download PDFInfo
- Publication number
- CN106984331B CN106984331B CN201710294612.XA CN201710294612A CN106984331B CN 106984331 B CN106984331 B CN 106984331B CN 201710294612 A CN201710294612 A CN 201710294612A CN 106984331 B CN106984331 B CN 106984331B
- Authority
- CN
- China
- Prior art keywords
- catalyst
- attapulgite
- preparation
- palladium
- attapulgite catalyst
- 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.)
- Expired - Fee Related
Links
- 239000003054 catalyst Substances 0.000 title claims abstract description 72
- 229960000892 attapulgite Drugs 0.000 title claims abstract description 48
- 229910052625 palygorskite Inorganic materials 0.000 title claims abstract description 48
- 229910017755 Cu-Sn Inorganic materials 0.000 title claims abstract description 33
- 229910017927 Cu—Sn Inorganic materials 0.000 title claims abstract description 33
- 238000002360 preparation method Methods 0.000 title claims abstract description 21
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims abstract description 26
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 22
- BDAGIHXWWSANSR-UHFFFAOYSA-N methanoic acid Natural products OC=O BDAGIHXWWSANSR-UHFFFAOYSA-N 0.000 claims abstract description 18
- 238000000034 method Methods 0.000 claims abstract description 17
- OSWFIVFLDKOXQC-UHFFFAOYSA-N 4-(3-methoxyphenyl)aniline Chemical compound COC1=CC=CC(C=2C=CC(N)=CC=2)=C1 OSWFIVFLDKOXQC-UHFFFAOYSA-N 0.000 claims abstract description 9
- 235000019253 formic acid Nutrition 0.000 claims abstract description 9
- 150000002940 palladium Chemical class 0.000 claims abstract description 7
- 229910021626 Tin(II) chloride Inorganic materials 0.000 claims abstract description 6
- 239000000725 suspension Substances 0.000 claims abstract description 5
- PIBWKRNGBLPSSY-UHFFFAOYSA-L palladium(II) chloride Chemical compound Cl[Pd]Cl PIBWKRNGBLPSSY-UHFFFAOYSA-L 0.000 claims description 4
- TXUICONDJPYNPY-UHFFFAOYSA-N (1,10,13-trimethyl-3-oxo-4,5,6,7,8,9,11,12,14,15,16,17-dodecahydrocyclopenta[a]phenanthren-17-yl) heptanoate Chemical compound C1CC2CC(=O)C=C(C)C2(C)C2C1C1CCC(OC(=O)CCCCCC)C1(C)CC2 TXUICONDJPYNPY-UHFFFAOYSA-N 0.000 claims description 2
- 229910021627 Tin(IV) chloride Inorganic materials 0.000 claims description 2
- 229940116318 copper carbonate Drugs 0.000 claims description 2
- ORTQZVOHEJQUHG-UHFFFAOYSA-L copper(II) chloride Chemical compound Cl[Cu]Cl ORTQZVOHEJQUHG-UHFFFAOYSA-L 0.000 claims description 2
- 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 2
- ARUVKPQLZAKDPS-UHFFFAOYSA-L copper(II) sulfate Chemical compound [Cu+2].[O-][S+2]([O-])([O-])[O-] ARUVKPQLZAKDPS-UHFFFAOYSA-L 0.000 claims description 2
- OPQARKPSCNTWTJ-UHFFFAOYSA-L copper(ii) acetate Chemical compound [Cu+2].CC([O-])=O.CC([O-])=O OPQARKPSCNTWTJ-UHFFFAOYSA-L 0.000 claims description 2
- GEZOTWYUIKXWOA-UHFFFAOYSA-L copper;carbonate Chemical compound [Cu+2].[O-]C([O-])=O GEZOTWYUIKXWOA-UHFFFAOYSA-L 0.000 claims description 2
- PNOXNTGLSKTMQO-UHFFFAOYSA-L diacetyloxytin Chemical compound CC(=O)O[Sn]OC(C)=O PNOXNTGLSKTMQO-UHFFFAOYSA-L 0.000 claims description 2
- 238000001704 evaporation Methods 0.000 claims description 2
- YJVFFLUZDVXJQI-UHFFFAOYSA-L palladium(ii) acetate Chemical compound [Pd+2].CC([O-])=O.CC([O-])=O YJVFFLUZDVXJQI-UHFFFAOYSA-L 0.000 claims description 2
- JKDRQYIYVJVOPF-FDGPNNRMSA-L palladium(ii) acetylacetonate Chemical compound [Pd+2].C\C([O-])=C\C(C)=O.C\C([O-])=C\C(C)=O JKDRQYIYVJVOPF-FDGPNNRMSA-L 0.000 claims description 2
- GPNDARIEYHPYAY-UHFFFAOYSA-N palladium(ii) nitrate Chemical compound [Pd+2].[O-][N+]([O-])=O.[O-][N+]([O-])=O GPNDARIEYHPYAY-UHFFFAOYSA-N 0.000 claims description 2
- 235000011150 stannous chloride Nutrition 0.000 claims description 2
- 239000001119 stannous chloride Substances 0.000 claims description 2
- RCIVOBGSMSSVTR-UHFFFAOYSA-L stannous sulfate Chemical compound [SnH2+2].[O-]S([O-])(=O)=O RCIVOBGSMSSVTR-UHFFFAOYSA-L 0.000 claims description 2
- 229910000375 tin(II) sulfate Inorganic materials 0.000 claims description 2
- HPGGPRDJHPYFRM-UHFFFAOYSA-J tin(iv) chloride Chemical compound Cl[Sn](Cl)(Cl)Cl HPGGPRDJHPYFRM-UHFFFAOYSA-J 0.000 claims description 2
- 235000019441 ethanol Nutrition 0.000 claims 4
- 150000003839 salts Chemical class 0.000 claims 3
- 238000006243 chemical reaction Methods 0.000 abstract description 42
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical class [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 abstract description 4
- 150000001879 copper Chemical class 0.000 abstract description 4
- 239000002994 raw material Substances 0.000 abstract description 3
- 238000009776 industrial production Methods 0.000 abstract description 2
- UGFAIRIUMAVXCW-UHFFFAOYSA-N Carbon monoxide Chemical compound [O+]#[C-] UGFAIRIUMAVXCW-UHFFFAOYSA-N 0.000 description 58
- 229910002091 carbon monoxide Inorganic materials 0.000 description 58
- 238000011156 evaluation Methods 0.000 description 32
- 239000010949 copper Substances 0.000 description 16
- KDLHZDBZIXYQEI-UHFFFAOYSA-N palladium Substances [Pd] KDLHZDBZIXYQEI-UHFFFAOYSA-N 0.000 description 14
- 229920004482 WACKER® Polymers 0.000 description 11
- 230000000694 effects Effects 0.000 description 11
- 239000007789 gas Substances 0.000 description 11
- 230000008859 change Effects 0.000 description 10
- 238000007254 oxidation reaction Methods 0.000 description 9
- 230000003647 oxidation Effects 0.000 description 8
- 230000003197 catalytic effect Effects 0.000 description 7
- 229910018072 Al 2 O 3 Inorganic materials 0.000 description 6
- 238000001354 calcination Methods 0.000 description 5
- 229910052802 copper Inorganic materials 0.000 description 5
- 238000011160 research Methods 0.000 description 5
- 229910021591 Copper(I) chloride Inorganic materials 0.000 description 4
- 238000006555 catalytic reaction Methods 0.000 description 4
- 229910000510 noble metal Inorganic materials 0.000 description 4
- 239000000243 solution Substances 0.000 description 4
- 229910002668 Pd-Cu Inorganic materials 0.000 description 3
- 101150003085 Pdcl gene Proteins 0.000 description 3
- 230000008901 benefit Effects 0.000 description 3
- 238000005516 engineering process Methods 0.000 description 3
- 230000010718 Oxidation Activity Effects 0.000 description 2
- 229910002666 PdCl2 Inorganic materials 0.000 description 2
- OXBLHERUFWYNTN-UHFFFAOYSA-M copper(I) chloride Chemical compound [Cu]Cl OXBLHERUFWYNTN-UHFFFAOYSA-M 0.000 description 2
- 238000001514 detection method Methods 0.000 description 2
- 230000003993 interaction Effects 0.000 description 2
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- 230000004048 modification Effects 0.000 description 2
- 238000012986 modification Methods 0.000 description 2
- 229910052763 palladium Inorganic materials 0.000 description 2
- 239000002245 particle Substances 0.000 description 2
- 239000010970 precious metal Substances 0.000 description 2
- 230000008569 process Effects 0.000 description 2
- 241000894007 species Species 0.000 description 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- 229910002651 NO3 Inorganic materials 0.000 description 1
- 241000208125 Nicotiana Species 0.000 description 1
- 235000002637 Nicotiana tabacum Nutrition 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 239000000969 carrier Substances 0.000 description 1
- 239000004927 clay Substances 0.000 description 1
- 238000004891 communication Methods 0.000 description 1
- 238000010276 construction Methods 0.000 description 1
- 230000001276 controlling effect Effects 0.000 description 1
- 229910000365 copper sulfate Inorganic materials 0.000 description 1
- 230000009849 deactivation Effects 0.000 description 1
- 238000013461 design Methods 0.000 description 1
- 230000008030 elimination Effects 0.000 description 1
- 238000003379 elimination reaction Methods 0.000 description 1
- 230000007613 environmental effect Effects 0.000 description 1
- 238000003912 environmental pollution Methods 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- 239000000446 fuel Substances 0.000 description 1
- 150000004820 halides Chemical class 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 238000005470 impregnation Methods 0.000 description 1
- 230000006872 improvement Effects 0.000 description 1
- 238000011065 in-situ storage Methods 0.000 description 1
- 230000000977 initiatory effect Effects 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 230000007246 mechanism Effects 0.000 description 1
- 150000004706 metal oxides Chemical class 0.000 description 1
- 239000002808 molecular sieve Substances 0.000 description 1
- 238000005457 optimization Methods 0.000 description 1
- 231100000572 poisoning Toxicity 0.000 description 1
- 230000000607 poisoning effect Effects 0.000 description 1
- 230000009467 reduction Effects 0.000 description 1
- 230000001105 regulatory effect Effects 0.000 description 1
- 230000004044 response Effects 0.000 description 1
- 238000007873 sieving Methods 0.000 description 1
- URGAHOPLAPQHLN-UHFFFAOYSA-N sodium aluminosilicate Chemical compound [Na+].[Al+3].[O-][Si]([O-])=O.[O-][Si]([O-])=O URGAHOPLAPQHLN-UHFFFAOYSA-N 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 230000004083 survival effect Effects 0.000 description 1
- 229910052718 tin Inorganic materials 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
- B01J23/00—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00
- B01J23/70—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of the iron group metals or copper
- B01J23/89—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of the iron group metals or copper combined with noble metals
- B01J23/8933—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of the iron group metals or copper combined with noble metals also combined with metals, or metal oxides or hydroxides provided for in groups B01J23/02 - B01J23/36
- B01J23/8966—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of the iron group metals or copper combined with noble metals also combined with metals, or metal oxides or hydroxides provided for in groups B01J23/02 - B01J23/36 with germanium, tin or lead
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
- 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
- B01D53/864—Removing carbon monoxide or hydrocarbons
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
- B01D2255/00—Catalysts
- B01D2255/10—Noble metals or compounds thereof
- B01D2255/102—Platinum group metals
- B01D2255/1023—Palladium
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
- B01D2255/00—Catalysts
- B01D2255/20—Metals or compounds thereof
- B01D2255/207—Transition metals
- B01D2255/20761—Copper
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
- B01D2255/00—Catalysts
- B01D2255/20—Metals or compounds thereof
- B01D2255/209—Other metals
- B01D2255/2094—Tin
Landscapes
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Environmental & Geological Engineering (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Health & Medical Sciences (AREA)
- Biomedical Technology (AREA)
- Analytical Chemistry (AREA)
- General Chemical & Material Sciences (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Materials Engineering (AREA)
- Organic Chemistry (AREA)
- Catalysts (AREA)
Abstract
本发明提供了一种Pd‑Cu‑Sn/凹凸棒土催化剂及其制备方法,制备步骤:称取适量钯盐、铜盐、锡盐和凹凸棒土,室温下与甲酸的水/乙醇溶液混合均匀,然后将该悬浊液在适当温度下缓慢蒸干,最后在N2/O2气氛中焙烧制得催化剂成品。该方法制备的催化剂适用条件范围广,可在反应温度‑60~200℃,空速1000~30000h‑1,CO含量10~20000ppm,原料气相对湿度10%~100%的反应条件下高效地催化氧化CO,并且失活催化剂易再生。本发明的催化剂制备工艺简单,操作性强,易于工业化生产,且成本低廉。
Description
技术领域
本发明涉及用于一氧化碳(CO)低温氧化的催化剂,具体为一种可用于高浓度水汽条件下的Pd-Cu-Sn/凹凸棒土催化剂及其制备方法。
背景技术
CO造成的环境污染涉及工业、军事、环保以及人类生活的各个方面,直接威胁着人类生存。CO低温催化氧化是消除CO的有效手段,在空气净化器、防毒面罩、烟草降害以及潜艇、航天器等密闭系统内CO消除方面均具有重要的实用价值。CO低温氧化催化剂主要有贵金属催化剂、非贵金属氧化物催化剂和负载型Wacker催化剂三大类。其中,负载型Wacker催化剂(PdCl2-CuCl2/载体)因其具有氧化物催化剂和贵金属催化剂难以比拟的抗水、抗卤化物中毒等优势,受到了广大科研工作者的青睐。
华东理工大学课题组开展了一系列以Al2O3为载体的负载型Wacker催化剂(Pd-Cu-Clx/Al2O3)的研究,结果表明,采用氨配位浸渍法或两步浸渍法制备的催化剂,在含少量水汽的反应条件下较常规浸渍法制得的催化剂表现出更优异的低温CO催化氧化活性,这主要得益于Cu2Cl(OH)3物种的存在及其与Pd物种间的强相互作用。然而在高浓度水汽条件下,各种方法制备的以Al2O3为载体的负载型Wacker催化剂均存在活性低,稳定性差等问题(Yuexin Shen,Guanzhong Lu,Yun Guo et al,Chemical Communication,2010,46:8433-8435;Xuexun Du,Huiying Li,Jun Yu et al,Catalysis Science&Technology,2015,5:3970-3979;Yafen Feng,Li Wang,Yanhui Zhang et al,Chinese Journal of Catalysis,2013,34:923-931)。我们课题组开展了以天然凹凸棒土(APT)为载体低贵金属含量的负载型Wacker催化剂(Pd-Cu/APT)设计和制备研究,考察了焙烧处理、制备方法以及载体改性等对Pd-Cu/APT催化CO氧化性能的影响(王永钊,程慧敏,范莉渊等,燃料化学学报,2014,42(5):597-602;Yongzhao Wang,Jing Shi,Ruifang Wu et al,Applied Clay Science,2016,119:126-131;Yongzhao Wang,Liyuan Fan,Jing Shi et al,Catalysis Letters,2015,145:1429-1435;Yongzhao Wang,Liyuan Fan,Ruifang Wu et al,Journal of FuelChemistry and Technology,2015,43(9):1076-1082;中国发明专利CN 103464170 B),结果表明,以凹凸棒土为载体的Pd-Cu/APT催化剂具有优异的低温CO催化氧化性能。虽然凹凸棒土较Al2O3廉价易得,且以其为载体的催化剂表现出更加优异的催化性能,但在高浓度水汽条件下,与以Al2O3为载体的Pd-Cu-Clx/Al2O3类似,Pd-Cu/APT也存在活性低,稳定性差等问题。针对上述问题,本课题组以及相关课题组继续围绕载体改性或选择新型结构载体构建高性能负载型Wacker催化剂开展探索,并取得了一定进展(Yongzhao Wang,YongningWang,Xiao Li et al,Environ Technol,DOI:10.1080/09593330.2017.1311944;FanyunZhou,Xuexun Du,Jun Yu et al,RSC Advances,2016,6:66553-66563)。
众所周知,负载型Wacker催化剂由经典均相Wacker催化剂(PdCl2-CuCl2水溶液)经固载化发展而来。目前,人们对负载型Wacker催化剂活性组分组成结构,催化反应作用机理的认识仍受对均相体系理解的影响,因此,对于负载型Wacker催化剂的改进提高,更多关注于载体选择、制备参数优化等方面,而对其经典的Pd、Cu二元活性组分的掺杂调控鲜见报道。
发明内容
本发明的目的是提供一种Pd-Cu-Sn/凹凸棒土催化剂及其制备方法,该方法制备的催化剂初活性高,稳定性好,适用范围广,尤其是在低温和高浓度水汽条件下可有效地催化氧化CO,且催化剂失活后易再生。该催化剂制备方法工艺简单,操作性强,易于工业化生产,同时贵金属含量更低,成本低廉。
本发明提供的一种Pd-Cu-Sn/凹凸棒土催化剂的制备方法,是以凹凸棒土为载体,制备在高浓度水汽条件下具有优异CO低温催化氧化活性的锡掺杂钯铜催化剂,具体包括如下步骤:
(1)配置浓度为0.5~3mol/L甲酸的水/乙醇溶液,所述的水/乙醇体积比为1:0.1~1;
(2)称取钯盐、铜盐、锡盐和凹凸棒土,室温下与甲酸的水/乙醇溶液混合均匀,形成悬浊液,所述的钯盐、铜盐、锡盐和凹凸棒土的质量比为1:5~75:5~75:50~300;
(3)将悬浊液在40~90℃下蒸干;
(4)在N2/O2气氛中于200~350℃焙烧1~6h,制得Pd-Cu-Sn/凹凸棒土催化剂,所述的N2/O2气氛体积比为1:0.1~1。
步骤(1)中所述的甲酸浓度为1~2.5mol/L;所述的水/乙醇体积比为1:0.2~0.8;
步骤(2)中所述的钯盐是氯化钯、硝酸钯、醋酸钯和乙酰丙酮钯中的一种或多种;所述的铜盐是氯化铜、硫酸铜、醋酸铜、硝酸铜和碳酸铜中的一种或多种;所述的锡盐是氯化亚锡、四氯化锡、硫酸亚锡和醋酸亚锡中的一种或多种。
步骤(3)中所述的蒸发温度为50~80℃。
步骤(4)中所述的N2/O2气氛体积比为1:0.2~0.5;所述的焙烧温度为250~300℃,时间为2~3h。
本发明制得的催化剂,在常压连续流动微反装置上进行CO催化氧化反应性能评价,催化剂装填量为0.30g。原料气先通过装有水的鼓泡器,通过控制鼓泡器的温度来调节原料气中的水汽浓度,然后再经过催化剂床层。采用Agilent 7890B型气相色谱仪在线分析原料气及尾气中CO、CO2浓度,其中色谱柱采用碳分子筛分离CO、CO2,柱后串联一个内装Ni催化剂的甲烷转化器,之后进入氢火焰检测器在线检测,最后经Chemstation工作站分析反应前后CO在混合气中的含量,CO最小检测量为1ppm。
与已有技术相比,本发明的优势在于:
(1)通过简单的Sn掺杂方式,对常规负载型Wacker催化剂的Pd、Cu二元活性组分进行调控,制备了具有高活性和高稳定性的CO低温氧化催化剂。
(2)催化剂适用条件范围更宽,可在反应温度-60~200℃,空速1000~30000h-1,CO含量10~20000ppm条件下高效地催化氧化CO。
(3)可在低温高浓度水汽条件下催化氧化CO,具有良好的催化稳定性,并且失活催化剂易再生。
(4)催化剂制备方法工艺更加简化,操作性强,易于工业化生产,同时贵金属含量更低,成本低廉。
具体实施方式
下面通过具体实施例对本发明进行详细说明,但不作为对本发明的限定。
实施例1
将20mg PdCl2,1.8204g CuCl2·2H2O,0.8860g SnCl4·5H2O和5g凹凸棒土载体加入到50mL 1mol/L甲酸的水/乙醇溶液中(水/乙醇体积比为5:1),搅拌混合均匀。将形成的悬浊液在70℃蒸干,然后在N2/O2气氛(体积比为5:1)条件下于300℃焙烧3h,制得Pd-Cu-Sn/凹凸棒土催化剂。筛分后取粒径为40-60目的颗粒备用。其中Pd负载量0.2wt%,Cu负载量11wt%,Sn负载量5wt%。
取0.30g催化剂,装入连续流动微反装置的反应管,通入原料气(CO含量为0.5%,相对湿度100%)进行反应,空速为10000h-1,反应温度为25℃,初始CO转化率达100%,并且维持CO完全转化至少300min。
实施例2
将实施例1中SnCl4·5H2O用量改为1.772g,采用同样的方法制得Pd-Cu-Sn/凹凸棒土催化剂,其中Pd负载量0.2wt%,Cu负载量11wt%,Sn负载量10wt%。
采用实施例1评价条件,在上述评价条件下,初始CO转化率达100%,并且维持CO完全转化至少500min。
实施例3
将实施例1中SnCl4·5H2O改为SnSO4,采用同样的方法制得Pd-Cu-Sn/凹凸棒土催化剂,其中Pd负载量0.2wt%,Cu负载量11wt%,Sn负载量5wt%。
采用实施例1评价条件,在上述评价条件下,初始CO转化率达100%,并且维持CO完全转化至少240min。
实施例4
将实施例1中PdCl2改为Pd(NO3)2,采用同样的方法制得Pd-Cu-Sn/凹凸棒土催化剂,其中Pd负载量0.2wt%,Cu负载量11wt%,Sn负载量5wt%。
采用实施例1评价条件,在上述评价条件下,初始CO转化率达100%,并且维持CO完全转化至少240min。
实施例5
将实施例1中PdCl2用量改为10mg,采用同样的方法制得Pd-Cu-Sn/凹凸棒土催化剂,其中Pd负载量0.1wt%,Cu负载量11wt%,Sn负载量5wt%。
采用实施例1评价条件,在上述评价条件下,初始CO转化率达100%,并且维持CO完全转化至少200min。
实施例6
将实施例1中CuCl2·2H2O改为Cu(NO3)2·3H2O,采用同样的方法制得Pd-Cu-Sn/凹凸棒土催化剂,其中Pd负载量0.2wt%,Cu负载量11wt%,Sn负载量5wt%。
采用实施例1评价条件,在上述评价条件下,初始CO转化率达100%,并且维持CO完全转化至少240min。
实施例7
将实施例1中甲酸浓度改为1.5mol/L,采用同样的方法制得Pd-Cu-Sn/凹凸棒土催化剂,其中Pd负载量0.2wt%,Cu负载量11wt%,Sn负载量5wt%。
采用实施例1评价条件,在上述评价条件下,初始CO转化率达100%,并且维持CO完全转化至少400min。
实施例8
将实施例1中水/乙醇溶液体积比改为2:1,采用同样的方法制得Pd-Cu-Sn/凹凸棒土催化剂,其中Pd负载量0.2wt%,Cu负载量11wt%,Sn负载量5wt%。
采用实施例1评价条件,在上述评价条件下,初始CO转化率达100%,并且维持CO完全转化至少400min。
实施例9
将实施例1中N2/O2气氛体积比改为2:1,采用同样的方法制得Pd-Cu-Sn/凹凸棒土催化剂,其中Pd负载量0.2wt%,Cu负载量11wt%,Sn负载量5wt%。
采用实施例1评价条件,在上述评价条件下,初始CO转化率达100%,并且维持CO完全转化至少500min。
实施例10
将实施例1中焙烧温度改为350℃,焙烧时间改为2h,采用同样的方法制得Pd-Cu-Sn/凹凸棒土催化剂,其中Pd负载量0.2wt%,Cu负载量11wt%,Sn负载量5wt%。
采用实施例1评价条件,在上述评价条件下,初始CO转化率达100%,并且维持CO完全转化至少300min。
实施例11
取实施例2制备的Pd-Cu-Sn/凹凸棒土催化剂,评价条件同实施例1,在上述评价条件下,待CO转化率降至50%以下时,切断原料气,在50℃对催化剂原位处理1h,然后通入原料气进行活性评价,CO转化率可达100%,并且维持CO完全转化至少400min。
实施例12
将实施例1评价条件中的原料气相对湿度改为70%,其他条件不变,取实施例2制备的Pd-Cu-Sn/凹凸棒土催化剂进行活性评价,初始CO转化率达100%,并且维持CO完全转化至少1000min。
实施例13
将实施例1评价条件中反应温度改为50℃,其他条件不变,取实施例2制备的Pd-Cu-Sn/凹凸棒土催化剂进行活性评价,初始CO转化率达100%,并且维持CO完全转化至少800min。
实施例14
将实施例1评价条件中的CO含量改为0.3%,其他条件不变,取实施例2制备的Pd-Cu-Sn/凹凸棒土催化剂进行活性评价,初始CO转化率达100%,并且维持CO完全转化至少800min。
实施例15
将实施例1评价条件中反应温度改为-20℃,其他条件不变,取实施例2制备的Pd-Cu-Sn/凹凸棒土催化剂进行活性评价,初始CO转化率达100%,并且维持CO完全转化至少400min。
实施例16
将实施例1评价条件中空速改为6000h-1,其他条件不变,取实施例2制备的Pd-Cu-Sn/凹凸棒土催化剂进行活性评价,初始CO转化率达100%,并且维持CO完全转化至少800min。
Claims (10)
1.一种Pd-Cu-Sn/凹凸棒土催化剂的制备方法,其特征在于,包括如下步骤:
(1)配置浓度为0.5~3mol/L甲酸的水/乙醇溶液,所述的水/乙醇体积比为1:0.1~1;
(2)称取钯盐、铜盐、锡盐和凹凸棒土,室温下与甲酸的水/乙醇溶液混合均匀,形成悬浊液,所述的钯盐、铜盐、锡盐和凹凸棒土的质量比为1:5~75:5~75:50~300;
(3)将悬浊液在40~90℃下蒸干;
(4)在N2/O2气氛中于200~350℃焙烧1~6h,制得Pd-Cu-Sn/凹凸棒土催化剂,所述的N2/O2气氛体积比为1:0.1~1。
2.如权利要求1所述的一种Pd-Cu-Sn/凹凸棒土催化剂的制备方法,其特征在于,所述步骤(1)中的甲酸浓度为1~2.5mol/L。
3.如权利要求1所述的一种Pd-Cu-Sn/凹凸棒土催化剂的制备方法,其特征在于,所述步骤(1)中的水/乙醇体积比为1:0.2~0.8。
4.如权利要求1所述的一种Pd-Cu-Sn/凹凸棒土催化剂的制备方法,其特征在于,所述步骤(2)中的钯盐是氯化钯、硝酸钯、醋酸钯和乙酰丙酮钯中的一种或多种。
5.如权利要求1所述的一种Pd-Cu-Sn/凹凸棒土催化剂的制备方法,其特征在于,所述步骤(2)中的铜盐是氯化铜、硫酸铜、醋酸铜、硝酸铜和碳酸铜中的一种或多种。
6.如权利要求1所述的一种Pd-Cu-Sn/凹凸棒土催化剂的制备方法,其特征在于,所述步骤(2)中的锡盐是氯化亚锡、四氯化锡、硫酸亚锡和醋酸亚锡中的一种或多种。
7.如权利要求1所述的一种Pd-Cu-Sn/凹凸棒土催化剂的制备方法,其特征在于,所述步骤(3)中的蒸发温度为50~80℃。
8.如权利要求1所述的一种Pd-Cu-Sn/凹凸棒土催化剂的制备方法,其特征在于,所述步骤(4)中的N2/O2气氛体积比为1:0.2~0.5。
9.如权利要求1所述的一种Pd-Cu-Sn/凹凸棒土催化剂的制备方法,其特征在于,所述步骤(4)中的焙烧温度为250~300℃,时间为2~3h。
10.如权利要求1-9所述任一方法制备的Pd-Cu-Sn/凹凸棒土催化剂。
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN201710294612.XA CN106984331B (zh) | 2017-04-28 | 2017-04-28 | 一种Pd-Cu-Sn/凹凸棒土催化剂及其制备方法 |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN201710294612.XA CN106984331B (zh) | 2017-04-28 | 2017-04-28 | 一种Pd-Cu-Sn/凹凸棒土催化剂及其制备方法 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| CN106984331A CN106984331A (zh) | 2017-07-28 |
| CN106984331B true CN106984331B (zh) | 2019-09-24 |
Family
ID=59417299
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CN201710294612.XA Expired - Fee Related CN106984331B (zh) | 2017-04-28 | 2017-04-28 | 一种Pd-Cu-Sn/凹凸棒土催化剂及其制备方法 |
Country Status (1)
| Country | Link |
|---|---|
| CN (1) | CN106984331B (zh) |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN109021291B (zh) * | 2018-09-18 | 2020-04-03 | 江苏宝源高新电工有限公司 | 一种凹凸棒石基高分子材料助剂及其制备方法和在制备阻燃高分子材料中的应用 |
Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN101428227A (zh) * | 2007-11-07 | 2009-05-13 | 中国科学院大连化学物理研究所 | 一种铱基双组分负载型催化剂及其制备和应用 |
| CN102101054A (zh) * | 2011-01-11 | 2011-06-22 | 山西大学 | 一种一氧化碳氧化催化剂及其制备方法 |
| CN104162433A (zh) * | 2014-08-04 | 2014-11-26 | 南昌大学 | 一种co低温氧化催化剂制备方法 |
-
2017
- 2017-04-28 CN CN201710294612.XA patent/CN106984331B/zh not_active Expired - Fee Related
Patent Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN101428227A (zh) * | 2007-11-07 | 2009-05-13 | 中国科学院大连化学物理研究所 | 一种铱基双组分负载型催化剂及其制备和应用 |
| CN102101054A (zh) * | 2011-01-11 | 2011-06-22 | 山西大学 | 一种一氧化碳氧化催化剂及其制备方法 |
| CN104162433A (zh) * | 2014-08-04 | 2014-11-26 | 南昌大学 | 一种co低温氧化催化剂制备方法 |
Non-Patent Citations (2)
| Title |
|---|
| Effect of Preparation Method on the Catalytic Activities of Pd–Cu/APT Catalysts for Low-Temperature CO Oxidation;Yongzhao Wang et al.;《Catalysis Letters》;20150428;第145卷(第7期);第1429-1435页 * |
| Steady-state co oxidation kinetics over the Pd(100) single crystal surface and the c(2×2)-Sn/Pd(100) bimetallic surface alloy;A.David Logan et al.;《Journal of Catalysis》;20040607;第133卷(第1期);第179-190页 * |
Also Published As
| Publication number | Publication date |
|---|---|
| CN106984331A (zh) | 2017-07-28 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| CN106540741B (zh) | 在室温下用于消除甲醛的催化剂及其制备方法 | |
| CN103736484B (zh) | 一种用于甲醛净化的负载型类整体式催化剂及其制备方法 | |
| CN101898137B (zh) | 一种用于CO低温氧化的Pd-Cu催化剂及制备方法 | |
| CN109201048A (zh) | 一种单原子催化剂及其制备方法 | |
| CN107308951A (zh) | 用于富氢气氛中优先氧化co的宽温催化剂的制备方法及其产品和应用 | |
| CN108421559A (zh) | 用于室温甲醛净化的全硅Beta分子筛催化剂及制备方法 | |
| CN106964348A (zh) | 一种甲醛污染物室温催化氧化催化剂及其制备方法和应用 | |
| CN112108145B (zh) | 一种氧化铝负载铱团簇催化剂及其制备与应用 | |
| Liu et al. | Catalytic oxidation degradation of volatile organic compounds (VOCs)–a review | |
| CN114471695B (zh) | 可高效降解含氰废气的催化剂及其制备方法和应用 | |
| CN103464170B (zh) | 一种Pd-Cu/改性凹凸棒石黏土催化剂的制备方法 | |
| CN108246351A (zh) | 用于室温甲醛净化的全硅zsm-5分子筛催化剂及制备方法 | |
| CN102626641A (zh) | 一种纳米复合催化剂及其制备方法 | |
| Wang et al. | Progress in degradation of volatile organic compounds by catalytic oxidation: a review based on the kinds of active components of catalysts | |
| CN107126962B (zh) | 一种氨氮废水处理用催化剂及其制备方法和应用 | |
| CN115400745A (zh) | 一种用于高效降解CVOCs的铈基催化剂 | |
| CN104324737A (zh) | 一种整体式常温低浓度一氧化碳催化剂及其制备和应用 | |
| CN112774667A (zh) | 一种负载型单原子铂催化剂及其制备方法和应用 | |
| CN115414963B (zh) | 一种用于去除VOCs的催化剂及其制备方法和用途 | |
| CN101698149B (zh) | 储存性能稳定的负载型金-pgm合金催化剂及其制备方法 | |
| CN110721680A (zh) | 一种用于同时催化氧化甲醛和co的催化剂及其制备方法和用途 | |
| CN113797935A (zh) | 一种用于低温高效处理VOCs的催化剂及其制备方法 | |
| CN115722220B (zh) | 一种催化氧化催化剂及其制备方法和应用 | |
| CN112973437A (zh) | 一种空气净化装置用甲醛去除母粒及其制备方法 | |
| JP4759739B2 (ja) | エチレン分解触媒 |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| PB01 | Publication | ||
| PB01 | Publication | ||
| SE01 | Entry into force of request for substantive examination | ||
| SE01 | Entry into force of request for substantive examination | ||
| GR01 | Patent grant | ||
| GR01 | Patent grant | ||
| CF01 | Termination of patent right due to non-payment of annual fee | ||
| CF01 | Termination of patent right due to non-payment of annual fee |
Granted publication date: 20190924 |