CN106590728A - A method for removing thiophene-like sulfur in fuel oil using Cu2O/SiO2‑Al2O3 composite airgel as an adsorbent - Google Patents
A method for removing thiophene-like sulfur in fuel oil using Cu2O/SiO2‑Al2O3 composite airgel as an adsorbent Download PDFInfo
- Publication number
- CN106590728A CN106590728A CN201611160480.3A CN201611160480A CN106590728A CN 106590728 A CN106590728 A CN 106590728A CN 201611160480 A CN201611160480 A CN 201611160480A CN 106590728 A CN106590728 A CN 106590728A
- Authority
- CN
- China
- Prior art keywords
- sio
- thiophene
- composite airgel
- sulfur
- adsorbent
- 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.)
- Granted
Links
- 239000002131 composite material Substances 0.000 title claims abstract description 72
- 239000003463 adsorbent Substances 0.000 title claims abstract description 43
- 239000000295 fuel oil Substances 0.000 title claims abstract description 32
- 238000000034 method Methods 0.000 title claims abstract description 30
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 title claims abstract description 17
- 229910052717 sulfur Inorganic materials 0.000 title claims abstract description 17
- 239000011593 sulfur Substances 0.000 title claims abstract description 17
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 title claims abstract description 8
- BERDEBHAJNAUOM-UHFFFAOYSA-N copper(I) oxide Inorganic materials [Cu]O[Cu] BERDEBHAJNAUOM-UHFFFAOYSA-N 0.000 title claims abstract 7
- 229910052593 corundum Inorganic materials 0.000 title claims abstract 7
- KRFJLUBVMFXRPN-UHFFFAOYSA-N cuprous oxide Chemical compound [O-2].[Cu+].[Cu+] KRFJLUBVMFXRPN-UHFFFAOYSA-N 0.000 title claims abstract 7
- 229910001845 yogo sapphire Inorganic materials 0.000 title claims abstract 7
- 239000010949 copper Substances 0.000 claims abstract description 98
- 238000001179 sorption measurement Methods 0.000 claims abstract description 93
- YTPLMLYBLZKORZ-UHFFFAOYSA-N Thiophene Chemical compound C=1C=CSC=1 YTPLMLYBLZKORZ-UHFFFAOYSA-N 0.000 claims abstract description 50
- FCEHBMOGCRZNNI-UHFFFAOYSA-N 1-benzothiophene Chemical compound C1=CC=C2SC=CC2=C1 FCEHBMOGCRZNNI-UHFFFAOYSA-N 0.000 claims abstract description 42
- 239000003502 gasoline Substances 0.000 claims abstract description 36
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 claims abstract description 32
- 229910052710 silicon Inorganic materials 0.000 claims abstract description 32
- 239000010703 silicon Substances 0.000 claims abstract description 32
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 claims abstract description 30
- 229910052802 copper Inorganic materials 0.000 claims abstract description 30
- 229930192474 thiophene Natural products 0.000 claims abstract description 26
- 229910052782 aluminium Inorganic materials 0.000 claims abstract description 19
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 claims abstract description 19
- BOTDANWDWHJENH-UHFFFAOYSA-N Tetraethyl orthosilicate Chemical compound CCO[Si](OCC)(OCC)OCC BOTDANWDWHJENH-UHFFFAOYSA-N 0.000 claims abstract description 14
- OPQARKPSCNTWTJ-UHFFFAOYSA-L copper(ii) acetate Chemical compound [Cu+2].CC([O-])=O.CC([O-])=O OPQARKPSCNTWTJ-UHFFFAOYSA-L 0.000 claims abstract description 14
- JGDITNMASUZKPW-UHFFFAOYSA-K aluminium trichloride hexahydrate Chemical compound O.O.O.O.O.O.Cl[Al](Cl)Cl JGDITNMASUZKPW-UHFFFAOYSA-K 0.000 claims abstract description 4
- 229940009861 aluminum chloride hexahydrate Drugs 0.000 claims abstract description 4
- 238000001035 drying Methods 0.000 claims abstract description 3
- 229910018072 Al 2 O 3 Inorganic materials 0.000 claims description 76
- 229910004298 SiO 2 Inorganic materials 0.000 claims description 75
- ZQRGREQWCRSUCI-UHFFFAOYSA-N [S].C=1C=CSC=1 Chemical compound [S].C=1C=CSC=1 ZQRGREQWCRSUCI-UHFFFAOYSA-N 0.000 claims description 22
- 230000009467 reduction Effects 0.000 claims description 18
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 5
- 229910052739 hydrogen Inorganic materials 0.000 claims description 5
- 239000001257 hydrogen Substances 0.000 claims description 5
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims description 3
- ORTQZVOHEJQUHG-UHFFFAOYSA-L copper(II) chloride Chemical group Cl[Cu]Cl ORTQZVOHEJQUHG-UHFFFAOYSA-L 0.000 claims description 3
- 235000019353 potassium silicate Nutrition 0.000 claims description 3
- NTHWMYGWWRZVTN-UHFFFAOYSA-N sodium silicate Chemical compound [Na+].[Na+].[O-][Si]([O-])=O NTHWMYGWWRZVTN-UHFFFAOYSA-N 0.000 claims description 3
- -1 ethyl orthosilicate Ester Chemical class 0.000 claims description 2
- 239000002994 raw material Substances 0.000 claims description 2
- 125000005605 benzo group Chemical group 0.000 claims 1
- 229910052681 coesite Inorganic materials 0.000 claims 1
- 229910052906 cristobalite Inorganic materials 0.000 claims 1
- 239000000377 silicon dioxide Substances 0.000 claims 1
- 235000012239 silicon dioxide Nutrition 0.000 claims 1
- 229910052682 stishovite Inorganic materials 0.000 claims 1
- 229910052905 tridymite Inorganic materials 0.000 claims 1
- 239000004964 aerogel Substances 0.000 abstract description 21
- 238000002360 preparation method Methods 0.000 abstract description 3
- 238000006243 chemical reaction Methods 0.000 abstract description 2
- 238000004587 chromatography analysis Methods 0.000 abstract description 2
- 230000000274 adsorptive effect Effects 0.000 abstract 1
- JBGWMRAMUROVND-UHFFFAOYSA-N 1-sulfanylidenethiophene Chemical class S=S1C=CC=C1 JBGWMRAMUROVND-UHFFFAOYSA-N 0.000 description 26
- 230000000694 effects Effects 0.000 description 19
- 238000006477 desulfuration reaction Methods 0.000 description 17
- 230000023556 desulfurization Effects 0.000 description 17
- 238000002474 experimental method Methods 0.000 description 16
- 230000007423 decrease Effects 0.000 description 9
- 238000005516 engineering process Methods 0.000 description 9
- 239000011148 porous material Substances 0.000 description 4
- IMNFDUFMRHMDMM-UHFFFAOYSA-N N-Heptane Chemical compound CCCCCCC IMNFDUFMRHMDMM-UHFFFAOYSA-N 0.000 description 3
- CSDREXVUYHZDNP-UHFFFAOYSA-N alumanylidynesilicon Chemical compound [Al].[Si] CSDREXVUYHZDNP-UHFFFAOYSA-N 0.000 description 3
- 229910044991 metal oxide Inorganic materials 0.000 description 3
- 150000004706 metal oxides Chemical class 0.000 description 3
- 230000008929 regeneration Effects 0.000 description 3
- 238000011069 regeneration method Methods 0.000 description 3
- 150000003577 thiophenes Chemical class 0.000 description 3
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Natural products CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 2
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 description 2
- 230000009471 action Effects 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- 230000008859 change Effects 0.000 description 2
- 239000007789 gas Substances 0.000 description 2
- 229910052751 metal Inorganic materials 0.000 description 2
- 239000002184 metal Substances 0.000 description 2
- 230000035515 penetration Effects 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 238000003786 synthesis reaction Methods 0.000 description 2
- 229920000742 Cotton Polymers 0.000 description 1
- 239000006004 Quartz sand Substances 0.000 description 1
- UCKMPCXJQFINFW-UHFFFAOYSA-N Sulphide Chemical compound [S-2] UCKMPCXJQFINFW-UHFFFAOYSA-N 0.000 description 1
- NPPHEVSPZGYDHP-UHFFFAOYSA-N [S].C1=CC=C2SC=CC2=C1 Chemical compound [S].C1=CC=C2SC=CC2=C1 NPPHEVSPZGYDHP-UHFFFAOYSA-N 0.000 description 1
- 238000009825 accumulation Methods 0.000 description 1
- 125000000218 acetic acid group Chemical group C(C)(=O)* 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 239000004480 active ingredient Substances 0.000 description 1
- 230000029936 alkylation Effects 0.000 description 1
- 238000005804 alkylation reaction Methods 0.000 description 1
- 239000002585 base Substances 0.000 description 1
- 230000009286 beneficial effect Effects 0.000 description 1
- 239000011230 binding agent Substances 0.000 description 1
- 239000000969 carrier Substances 0.000 description 1
- 150000001768 cations Chemical class 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 238000010668 complexation reaction Methods 0.000 description 1
- 239000008139 complexing agent Substances 0.000 description 1
- WCCJDBZJUYKDBF-UHFFFAOYSA-N copper silicon Chemical compound [Si].[Cu] WCCJDBZJUYKDBF-UHFFFAOYSA-N 0.000 description 1
- 230000003247 decreasing effect Effects 0.000 description 1
- 230000018109 developmental process Effects 0.000 description 1
- 238000003912 environmental pollution Methods 0.000 description 1
- 238000000605 extraction Methods 0.000 description 1
- 230000036541 health Effects 0.000 description 1
- 238000009776 industrial production Methods 0.000 description 1
- 229910021645 metal ion Inorganic materials 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- 239000002808 molecular sieve Substances 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 239000003208 petroleum Substances 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
- 238000003980 solgel method Methods 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 238000005987 sulfurization reaction Methods 0.000 description 1
- 150000003568 thioethers Chemical class 0.000 description 1
- 229910052723 transition metal Inorganic materials 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
- 239000011787 zinc oxide Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10G—CRACKING HYDROCARBON OILS; PRODUCTION OF LIQUID HYDROCARBON MIXTURES, e.g. BY DESTRUCTIVE HYDROGENATION, OLIGOMERISATION, POLYMERISATION; RECOVERY OF HYDROCARBON OILS FROM OIL-SHALE, OIL-SAND, OR GASES; REFINING MIXTURES MAINLY CONSISTING OF HYDROCARBONS; REFORMING OF NAPHTHA; MINERAL WAXES
- C10G25/00—Refining of hydrocarbon oils in the absence of hydrogen, with solid sorbents
- C10G25/003—Specific sorbent material, not covered by C10G25/02 or C10G25/03
-
- 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
- B01J20/00—Solid sorbent compositions or filter aid compositions; Sorbents for chromatography; Processes for preparing, regenerating or reactivating thereof
- B01J20/02—Solid sorbent compositions or filter aid compositions; Sorbents for chromatography; Processes for preparing, regenerating or reactivating thereof comprising inorganic material
- B01J20/06—Solid sorbent compositions or filter aid compositions; Sorbents for chromatography; Processes for preparing, regenerating or reactivating thereof comprising inorganic material comprising oxides or hydroxides of metals not provided for in group B01J20/04
-
- 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
- B01J20/00—Solid sorbent compositions or filter aid compositions; Sorbents for chromatography; Processes for preparing, regenerating or reactivating thereof
- B01J20/02—Solid sorbent compositions or filter aid compositions; Sorbents for chromatography; Processes for preparing, regenerating or reactivating thereof comprising inorganic material
- B01J20/06—Solid sorbent compositions or filter aid compositions; Sorbents for chromatography; Processes for preparing, regenerating or reactivating thereof comprising inorganic material comprising oxides or hydroxides of metals not provided for in group B01J20/04
- B01J20/08—Solid sorbent compositions or filter aid compositions; Sorbents for chromatography; Processes for preparing, regenerating or reactivating thereof comprising inorganic material comprising oxides or hydroxides of metals not provided for in group B01J20/04 comprising aluminium oxide or hydroxide; comprising bauxite
-
- 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
- B01J20/00—Solid sorbent compositions or filter aid compositions; Sorbents for chromatography; Processes for preparing, regenerating or reactivating thereof
- B01J20/02—Solid sorbent compositions or filter aid compositions; Sorbents for chromatography; Processes for preparing, regenerating or reactivating thereof comprising inorganic material
- B01J20/10—Solid sorbent compositions or filter aid compositions; Sorbents for chromatography; Processes for preparing, regenerating or reactivating thereof comprising inorganic material comprising silica or silicate
- B01J20/103—Solid sorbent compositions or filter aid compositions; Sorbents for chromatography; Processes for preparing, regenerating or reactivating thereof comprising inorganic material comprising silica or silicate comprising silica
-
- 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
- B01J20/00—Solid sorbent compositions or filter aid compositions; Sorbents for chromatography; Processes for preparing, regenerating or reactivating thereof
- B01J20/28—Solid sorbent compositions or filter aid compositions; Sorbents for chromatography; Processes for preparing, regenerating or reactivating thereof characterised by their form or physical properties
- B01J20/28014—Solid sorbent compositions or filter aid compositions; Sorbents for chromatography; Processes for preparing, regenerating or reactivating thereof characterised by their form or physical properties characterised by their form
- B01J20/28047—Gels
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10G—CRACKING HYDROCARBON OILS; PRODUCTION OF LIQUID HYDROCARBON MIXTURES, e.g. BY DESTRUCTIVE HYDROGENATION, OLIGOMERISATION, POLYMERISATION; RECOVERY OF HYDROCARBON OILS FROM OIL-SHALE, OIL-SAND, OR GASES; REFINING MIXTURES MAINLY CONSISTING OF HYDROCARBONS; REFORMING OF NAPHTHA; MINERAL WAXES
- C10G2300/00—Aspects relating to hydrocarbon processing covered by groups C10G1/00 - C10G99/00
- C10G2300/20—Characteristics of the feedstock or the products
- C10G2300/201—Impurities
- C10G2300/202—Heteroatoms content, i.e. S, N, O, P
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Analytical Chemistry (AREA)
- Inorganic Chemistry (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Dispersion Chemistry (AREA)
- Engineering & Computer Science (AREA)
- General Chemical & Material Sciences (AREA)
- Solid-Sorbent Or Filter-Aiding Compositions (AREA)
- Production Of Liquid Hydrocarbon Mixture For Refining Petroleum (AREA)
Abstract
Description
技术领域technical field
本发明属于燃料油加工技术领域，具体涉及一种吸附条件温和、制备方法简单的以Cu2O/SiO2-Al2O3复合气凝胶为吸附剂通过π络合吸附作用脱除燃料油中噻吩类硫的方法。The invention belongs to the technical field of fuel oil processing, and in particular relates to a method of removing fuel oil through π complex adsorption using Cu 2 O/SiO 2 -Al 2 O 3 composite airgel as an adsorbent with mild adsorption conditions and simple preparation method The method of sulfur in thiophene class.
背景技术Background technique
随着车用工业的大力发展，汽车尾气硫化物的大量排放不仅使环境污染问题日趋严重，同样也威胁着人类的身体健康。因此，对燃料油的深度脱硫已经成为了全社会关注的焦点。With the vigorous development of the automobile industry, the large amount of sulfide emissions from automobile exhaust not only makes environmental pollution more and more serious, but also threatens human health. Therefore, the deep desulfurization of fuel oil has become the focus of attention of the whole society.
目前，燃料油品的脱硫工艺主要有加氢脱硫技术、烷基化脱硫技术、生物脱硫技术、萃取脱硫技术、氧化脱硫技术、吸附脱硫技术等。其中，π络合吸附脱硫技术以其较好的脱硫效果、简便的操作和低廉的成本等优点在该技术领域中脱颖而出。根据载体的不同，π络合脱硫吸附剂可分为分子筛类、活性炭类、金属氧化物类。At present, the desulfurization technology of fuel oil mainly includes hydrodesulfurization technology, alkylation desulfurization technology, biological desulfurization technology, extraction desulfurization technology, oxidation desulfurization technology, adsorption desulfurization technology, etc. Among them, the π complex adsorption desulfurization technology stands out in this technical field because of its good desulfurization effect, simple operation and low cost. According to different carriers, π-complex desulfurization adsorbents can be divided into molecular sieves, activated carbons, and metal oxides.
以金属氧化物为载体的π络合脱硫吸附剂。南通大学（公开号 CN 10300787 A）以铜元素掺杂的介孔γ-Al2O3与含硫的燃料油接触，利用吸附法实现脱硫，操作成本低，吸附容量大，且再生方便。中国石油化工股份有限公司（公开号 CN 10161923 A）制备了一种脱硫吸附剂，该吸附剂包括以氧化铝为粘结剂，氧化锌为载体，再与络合剂溶液接触，然后负载金属促进剂。用于燃料油脱硫，活性高，吸附硫容量大。但在制备过程中，金属离子容易堵塞金属氧化物孔道，导致负载的活性组分在表面堆积，无法进入孔道内提供活性位，降低吸附脱硫性能，且此法较难应用于工业化生产。π-complex desulfurization adsorbent with metal oxide as carrier. Nantong University (publication number CN 10300787 A) contacted mesoporous γ-Al 2 O 3 doped with copper elements with sulfur-containing fuel oil, and achieved desulfurization by adsorption method. The operation cost is low, the adsorption capacity is large, and regeneration is convenient. China Petroleum & Chemical Corporation (publication number CN 10161923 A) prepared a desulfurization adsorbent, which includes alumina as a binder and zinc oxide as a carrier, then contacts with a complexing agent solution, and then loads metals to promote agent. It is used for desulfurization of fuel oil, with high activity and large adsorption capacity of sulfur. However, during the preparation process, metal ions are easy to block the pores of metal oxides, resulting in the accumulation of loaded active components on the surface, which cannot enter the pores to provide active sites, reducing the adsorption and desulfurization performance, and this method is difficult to apply to industrial production.
发明内容Contents of the invention
针对现有π络合吸附剂在脱除燃料油中噻吩类硫中存在的上述问题，本发明的目的在于提供一种吸附条件温和、操作方便、吸附性能优越且吸附容量大、易再生的Cu2O/SiO2-Al2O3复合气凝胶通过π络合吸附作用脱除燃料油中噻吩类硫的以Cu2O/SiO2-Al2O3复合气凝胶为吸附剂通过π络合吸附作用脱除燃料油中噻吩类硫的方法。In view of the above-mentioned problems existing in the existing π-complexed adsorbent in the removal of thiophene sulfur in fuel oil, the purpose of the present invention is to provide a Cu with mild adsorption conditions, convenient operation, superior adsorption performance, large adsorption capacity, and easy regeneration. 2 O / SiO 2 -Al 2 O 3 composite airgel to remove thiophene sulfur from fuel oil by π complex adsorption A method for removing thiophene sulfur from fuel oil by complex adsorption.
所述的一种以Cu2O/SiO2-Al2O3复合气凝胶为吸附剂脱除燃料油中噻吩类硫的方法，其特征在于以Cu2O/SiO2-Al2O3复合气凝胶为吸附剂，将该吸附剂填装入固定床吸附装置，在吸附温度为0~100 ℃，空速为1~10 h-1下向固定床吸附装置中通入含有噻吩类硫的模拟汽油，经吸附后得到无硫的模拟汽油。The method for removing thiophene sulfur in fuel oil by using Cu 2 O/SiO 2 -Al 2 O 3 composite airgel as an adsorbent is characterized in that the Cu 2 O/SiO 2 -Al 2 O 3 The composite airgel is used as the adsorbent, and the adsorbent is filled into the fixed bed adsorption device, and the thiophene - containing Sulfur simulated gasoline, sulfur-free simulated gasoline can be obtained after adsorption.
所述的一种以Cu2O/SiO2-Al2O3复合气凝胶为吸附剂脱除燃料油中噻吩类硫的方法，其特征在于噻吩类硫为噻吩或苯并噻吩。The method for removing thiophene-like sulfur in fuel oil by using Cu 2 O/SiO 2 -Al 2 O 3 composite airgel as an adsorbent is characterized in that the thiophene-like sulfur is thiophene or benzothiophene.
所述的一种以Cu2O/SiO2-Al2O3复合气凝胶为吸附剂脱除燃料油中噻吩类硫的方法，其特征在于Cu2O/SiO2-Al2O3复合气凝胶吸附剂以硅源、铝源和铜源为原料，采用溶胶凝胶—常压干燥法制备得到CuO/SiO2-Al2O3复合气凝胶，CuO/SiO2-Al2O3复合气凝胶经氢气还原得Cu2O/SiO2-Al2O3复合气凝胶。The method for removing thiophene sulfur in fuel oil by using Cu 2 O/SiO 2 -Al 2 O 3 composite airgel as an adsorbent is characterized in that Cu 2 O/SiO 2 -Al 2 O 3 composite The airgel adsorbent uses silicon source, aluminum source and copper source as raw materials to prepare CuO/SiO 2 -Al 2 O 3 composite airgel by sol-gel-atmospheric pressure drying method, CuO/SiO 2 -Al 2 O 3 Composite airgel was reduced by hydrogen to obtain Cu 2 O/SiO 2 -Al 2 O 3 composite airgel.
所述以Cu2O/SiO2-Al2O3复合气凝胶为吸附剂脱除燃料油中噻吩类硫的方法，其特征在于所用的硅源为正硅酸乙酯或水玻璃，优选为正硅酸乙酯；铝源为六水合氯化铝；铜源为氯化铜或醋酸铜，优选为醋酸铜。The method for removing thiophene sulfur in fuel oil by using Cu 2 O/SiO 2 -Al 2 O 3 composite airgel as an adsorbent is characterized in that the silicon source used is tetraethyl orthosilicate or water glass, preferably It is ethyl orthosilicate; the aluminum source is aluminum chloride hexahydrate; the copper source is copper chloride or copper acetate, preferably copper acetate.
所述的一种以Cu2O/SiO2-Al2O3复合气凝胶为吸附剂脱除燃料油中噻吩类硫的方法，其特征在于Cu2O/SiO2-Al2O3复合气凝胶吸附剂中的硅、铝摩尔比为2~19 : 1，优选为4~19 : 1，最优为9：1。The method for removing thiophene sulfur in fuel oil by using Cu 2 O/SiO 2 -Al 2 O 3 composite airgel as an adsorbent is characterized in that Cu 2 O/SiO 2 -Al 2 O 3 composite The molar ratio of silicon and aluminum in the airgel adsorbent is 2-19:1, preferably 4-19:1, and optimally 9:1.
所述的一种以Cu2O/SiO2-Al2O3复合气凝胶为吸附剂脱除燃料油中噻吩类硫的方法，其特征在于Cu2O/SiO2-Al2O3复合气凝胶吸附剂中硅与铝总摩尔量与铜摩尔量比为40~150：1，优选为40：1、50：1、75：1。The method for removing thiophene sulfur in fuel oil by using Cu 2 O/SiO 2 -Al 2 O 3 composite airgel as an adsorbent is characterized in that Cu 2 O/SiO 2 -Al 2 O 3 composite The ratio of the total molar mass of silicon and aluminum to the molar mass of copper in the airgel adsorbent is 40-150:1, preferably 40:1, 50:1, 75:1.
所述以Cu2O/SiO2-Al2O3复合气凝胶为吸附剂脱除燃料油中噻吩类硫的方法，其特征在于CuO/SiO2-Al2O3复合气凝胶经氢气还原成Cu2O/SiO2-Al2O3复合气凝胶的还原温度为100~220℃，优选为100~160 ℃，还原时间为3~7h，优选为4~6h。The method for removing thiophene sulfur in fuel oil by using Cu 2 O/SiO 2 -Al 2 O 3 composite airgel as an adsorbent is characterized in that the CuO/SiO 2 -Al 2 O 3 composite airgel is treated with hydrogen The reduction temperature for reducing to Cu 2 O/SiO 2 -Al 2 O 3 composite airgel is 100-220°C, preferably 100-160°C, and the reduction time is 3-7h, preferably 4-6h.
所述的一种以Cu2O/SiO2-Al2O3复合气凝胶为吸附剂脱除燃料油中噻吩类硫的方法，其特征在于通入噻吩或苯并噻吩的空速为1~5 h-1。The method for removing thiophene-like sulfur in fuel oil using Cu 2 O/SiO 2 -Al 2 O 3 composite airgel as an adsorbent is characterized in that the space velocity of feeding thiophene or benzothiophene is 1 ~5 h -1 .
所述的一种以Cu2O/SiO2-Al2O3复合气凝胶为吸附剂脱除燃料油中噻吩类硫的方法，其特征在于吸附温度为0~40 ℃。The method for removing thiophene sulfur in fuel oil by using Cu 2 O/SiO 2 -Al 2 O 3 composite airgel as an adsorbent is characterized in that the adsorption temperature is 0-40°C.
所述的一种以Cu2O/SiO2-Al2O3复合气凝胶为吸附剂脱除燃料油中噻吩类硫的方法，其特征在于Cu2O/SiO2-Al2O3复合气凝胶吸附模拟汽油中噻吩类硫的浓度为100 ppm~2000 ppm，优选为100~500 ppm。The method for removing thiophene sulfur in fuel oil by using Cu 2 O/SiO 2 -Al 2 O 3 composite airgel as an adsorbent is characterized in that Cu 2 O/SiO 2 -Al 2 O 3 composite The airgel adsorption simulates the concentration of thiophene sulfur in gasoline in the range of 100 ppm to 2000 ppm, preferably 100 to 500 ppm.
通过采用上述技术，与现有技术相比，本发明的有益效果如下：By adopting above-mentioned technology, compared with prior art, the beneficial effect of the present invention is as follows:
1）本发明的Cu2O/SiO2-Al2O3复合气凝胶具有典型介孔特征孔径(5~20 nm)，高孔隙率(85~99%)，高比表面积(600~1500 m2/g)等独特物理化学性质，因此噻吩类硫化物可无阻碍地进入气凝胶孔道内，且活性组分与硫化物能充分接触；1) The Cu 2 O/SiO 2 -Al 2 O 3 composite airgel of the present invention has a typical mesoporous characteristic pore size (5-20 nm), high porosity (85-99%), and high specific surface area (600-1500 m 2 /g) and other unique physical and chemical properties, so thiophene sulfides can enter the airgel pores without hindrance, and the active components can fully contact with the sulfides;
2）本发明的Cu2O/SiO2-Al2O3复合气凝胶作为π络合脱硫吸附剂与其他π络合吸附剂相比，它在硅骨架结构中引入Al3+，Al3+是L酸，由于S—M（M为金属阳离子）作用，可以通过Al3+ 与S2- 的酸碱作用加强吸附剂对硫的吸附，其结构是由纳米级骨架颗粒构成，使骨架内的活性组分可充分暴露。在气凝胶的合成过程中，可将具有π络合作用的过渡金属盐加入其中，因此其活性组分的量是可调节的；2) The Cu 2 O/SiO 2 -Al 2 O 3 composite airgel of the present invention is used as a π-complex desulfurization adsorbent. Compared with other π-complex adsorbents, it introduces Al 3+ , Al 3 + is L acid, due to the action of S—M (M is a metal cation), the adsorption of sulfur by the adsorbent can be strengthened through the acid-base action of Al 3+ and S 2- , and its structure is composed of nano-scale skeleton particles, so that the skeleton The active ingredients in it can be fully exposed. During the synthesis of airgel, transition metal salts with π complexation can be added to it, so the amount of active components can be adjusted;
3）本发明的Cu2O/SiO2-Al2O3复合气凝胶π络合吸附剂对噻吩类硫化物有良好的吸附性能，通过溶剂洗涤便可再生，再生后仍然有良好的吸附性能；3) The Cu 2 O/SiO 2 -Al 2 O 3 composite airgel π complex adsorbent of the present invention has good adsorption performance for thiophene sulfides, can be regenerated by solvent washing, and still has good adsorption after regeneration performance;
4）本发明的吸附反应在常压下进行、吸附条件温和、对吸附设备的要求低、操作方便，且对噻吩类化合物有良好的吸附效果。4) The adsorption reaction of the present invention is carried out under normal pressure, the adsorption conditions are mild, the requirements for adsorption equipment are low, the operation is convenient, and it has good adsorption effect on thiophene compounds.
具体实施方式detailed description
下面结合具体实施例对本发明进行进一步描述，但本发明的保护范围并不仅限于此。The present invention will be further described below in conjunction with specific examples, but the protection scope of the present invention is not limited thereto.
实施例1-6：不同硅源与铜源的Cu2O/SiO2-Al2O3复合气凝胶对吸附模拟汽油中噻吩类硫化物的影响Example 1-6: Effect of Cu 2 O/SiO 2 -Al 2 O 3 composite aerogels with different silicon and copper sources on the adsorption of thiophene sulfides in simulated gasoline
选用溶胶-凝胶法制备，固定硅铝总摩尔量与铜摩尔量比50、硅铝比9、氢气还原温度120摄氏度下还原5h的Cu2O/SiO2-Al2O3复合气凝胶，所用的硅源有正硅酸乙酯、水玻璃，铜源有氯化铜、醋酸铜，铝源为六水合氯化铝，将制备完成的Cu2O/SiO2-Al2O3复合气凝胶进行穿透吸附脱硫实验，具体操作如下： 在固定床反应器中，最底层填装适量的脱脂棉，然后填装1 g的Cu2O/SiO2-Al2O3气凝胶与适量的石英砂。吸附实验开始前，用正庚烷充分润湿所填装的吸附剂。通入模拟汽油，在反应器的下端出口处收集吸附后的模拟汽油，进行气相色谱分析。操作条件为进料采用100ppm的噻吩或苯并噻吩，固定吸附温度25℃，固定空速1 h-1；所得到的噻吩与苯并噻吩的穿透吸附容量，结果见表1。Prepared by sol-gel method, fixed Cu 2 O/SiO 2 -Al 2 O 3 composite airgel with a total molar ratio of silicon and aluminum to copper molar ratio of 50, a ratio of silicon to aluminum of 9, and a hydrogen reduction temperature of 120 degrees Celsius for 5 hours , the silicon source used is tetraethyl orthosilicate and water glass, the copper source is copper chloride and copper acetate, the aluminum source is aluminum chloride hexahydrate, and the prepared Cu 2 O/SiO 2 -Al 2 O 3 composite Airgel was subjected to breakthrough adsorption desulfurization experiment, and the specific operation was as follows: In the fixed bed reactor, an appropriate amount of absorbent cotton was filled in the bottom layer, and then 1 g of Cu 2 O/SiO 2 -Al 2 O 3 airgel was filled with Appropriate amount of quartz sand. Before the adsorption experiment started, the packed adsorbent was fully wetted with n-heptane. Feed simulated gasoline, and collect the adsorbed simulated gasoline at the outlet of the lower end of the reactor for gas chromatographic analysis. The operating conditions are 100ppm thiophene or benzothiophene as feed, fixed adsorption temperature at 25°C, and fixed space velocity at 1 h -1 ; see Table 1 for the breakthrough adsorption capacity of obtained thiophene and benzothiophene.
表1 不同硅源的Cu2O/SiO2-Al2O3复合气凝胶对模拟汽油中噻吩类硫化物的吸附性能Table 1 Adsorption properties of Cu 2 O/SiO 2 -Al 2 O 3 composite aerogels with different silicon sources for thiophene sulfides in simulated gasoline
表2 不同铜源的Cu2O/SiO2-Al2O3复合气凝胶对模拟汽油中噻吩类硫化物的吸附性能Table 2 Adsorption performance of Cu 2 O/SiO 2 -Al 2 O 3 composite aerogels with different copper sources on thiophene sulfides in simulated gasoline
从表1、表2可以看出，在合成Cu2O/SiO2-Al2O3复合气凝胶所用的硅源与铜源中，当硅源选用正硅酸乙酯，铜源选用醋酸铜时，所合成的Cu2O/SiO2-Al2O3复合气凝胶在穿透吸附实验中，对噻吩与苯并噻吩有最大的穿透吸附容量。因此优选硅源为正硅酸乙酯，铜源为醋酸铜。It can be seen from Table 1 and Table 2 that in the silicon source and copper source used in the synthesis of Cu 2 O/SiO 2 -Al 2 O 3 composite airgel, when the silicon source is tetraethyl orthosilicate and the copper source is acetic acid When copper is used, the synthesized Cu 2 O/SiO 2 -Al 2 O 3 composite airgel has the largest breakthrough adsorption capacity for thiophene and benzothiophene in the breakthrough adsorption experiment. Therefore, it is preferred that the silicon source is ethyl orthosilicate and the copper source is copper acetate.
实施例7-10：不同硅铝摩尔比的Cu2O/SiO2-Al2O3复合气凝胶对吸附模拟汽油中噻吩类硫化物的影响Examples 7-10: Effects of Cu 2 O/SiO 2 -Al 2 O 3 composite aerogels with different molar ratios of silicon and aluminum on the adsorption of thiophene sulfides in simulated gasoline
选用硅源为正硅酸乙酯、铜源为醋酸铜，硅铝摩尔比分别2、4、9、19，其他条件同实施案例1~6的Cu2O/SiO2-Al2O3气凝胶，对模拟汽油中噻吩类硫化物进行穿透吸附实验。其穿透吸附实验操作同实施例1~6，吸附结果见表3。The silicon source is tetraethyl orthosilicate, the copper source is copper acetate, the molar ratio of silicon to aluminum is 2, 4, 9, 19, and other conditions are the same as the Cu 2 O/SiO 2 -Al 2 O 3 gas in the implementation cases 1~6. Gel, breakthrough adsorption experiments on thiophene sulfides in simulated gasoline. The operation of the breakthrough adsorption experiment is the same as in Examples 1-6, and the adsorption results are shown in Table 3.
表3 不同硅铝比对吸附模拟汽油中噻吩类硫化物的影响Table 3 Effects of different silicon-aluminum ratios on the adsorption of thiophene sulfides in simulated gasoline
从表3可以看出，Cu2O/SiO2-Al2O3气凝胶随着硅铝摩尔比的减小即铝含量的增加，对噻吩与苯并噻吩的穿透吸附容量随之先增后降。在硅铝摩尔比为9时，噻吩与苯并噻吩的穿透吸附容量达到最大，因此优选硅铜摩尔比为4~19的Cu2O/SiO2-Al2O3气凝胶。It can be seen from Table 3 that the breakthrough adsorption capacity of Cu 2 O/SiO 2 -Al 2 O 3 airgel for thiophene and benzothiophene increases with the decrease of the silicon-aluminum molar ratio, that is, the increase of aluminum content. Decrease after increase. When the silicon-aluminum molar ratio is 9, the breakthrough adsorption capacity of thiophene and benzothiophene reaches the maximum, so Cu 2 O/SiO 2 -Al 2 O 3 aerogels with a silicon-copper molar ratio of 4-19 are preferred.
实施例11-14：不同硅铜摩尔比的Cu2O/SiO2-Al2O3复合气凝胶对吸附模拟汽油中噻吩类硫化物的影响Examples 11-14: Effects of Cu 2 O/SiO 2 -Al 2 O 3 composite aerogels with different molar ratios of silicon and copper on the adsorption of thiophene sulfides in simulated gasoline
选用硅源为正硅酸乙酯、铜源为醋酸铜，硅铜比为40、50、75、150 ，其他条件同实施案例1~6的Cu2O/SiO2-Al2O3，其他条件同实施案例1~6，对模拟汽油中噻吩类硫化物进行穿透吸附实验。其穿透吸附实验操作同实施例1~6，吸附结果见表4。The silicon source is tetraethyl orthosilicate, the copper source is copper acetate, the ratio of silicon to copper is 40, 50, 75, 150, and other conditions are the same as Cu 2 O/SiO 2 -Al 2 O 3 in the implementation cases 1~6, and other The conditions are the same as the implementation cases 1~6, and the breakthrough adsorption experiment is carried out on the thiophene sulfides in the simulated gasoline. The operation of the breakthrough adsorption experiment is the same as in Examples 1-6, and the adsorption results are shown in Table 4.
表4 不同硅与铝总摩尔量与铜摩尔量比的Cu2O/SiO2-Al2O3对吸附模拟汽油中噻吩类硫化物的影响Table 4 Effects of Cu 2 O/SiO 2 -Al 2 O 3 with different molar ratios of silicon and aluminum to copper on the adsorption of thiophene sulfides in simulated gasoline
从表4可以看出，Cu2O/SiO2-Al2O3气凝胶随着硅与铝总摩尔量与铜摩尔量比的减小即铜含量的增加，对噻吩与苯并噻吩的穿透吸附容量随之先增后降。在硅与铝总摩尔量与铜摩尔量比为50时，噻吩与苯并噻吩的穿透吸附容量达到最大，因此优选硅与铝总摩尔量与铜摩尔量比为40~75的Cu2O/SiO2-Al2O3气凝胶。It can be seen from Table 4 that the Cu 2 O/SiO 2 -Al 2 O 3 aerogel has a greater effect on thiophene and benzothiophene as the ratio of the total molar mass of silicon and aluminum to copper molar mass decreases, that is, the copper content increases. The breakthrough adsorption capacity increases first and then decreases. When the total molar ratio of silicon and aluminum to copper is 50, the breakthrough adsorption capacity of thiophene and benzothiophene reaches the maximum, so Cu 2 O with a total molar ratio of silicon and aluminum to copper of 40-75 is preferred. /SiO 2 -Al 2 O 3 airgel.
实施例15-21：CuO/SiO2-Al2O3复合气凝胶在不同还原温度下还原所得的Cu2O/SiO2-Al2O3复合气凝胶对吸附模拟汽油中噻吩类硫化物的影响Examples 15-21: CuO/SiO 2 -Al 2 O 3 composite aerogels were reduced at different reduction temperatures to obtain Cu 2 O/SiO 2 -Al 2 O 3 composite aerogels on the adsorption of thiophenes in simulated gasoline sulfuration Effect of things
选用硅源为正硅酸乙酯、铜源为醋酸铜，还原温度分别为100、120、1400、160、180、200、220℃，其他条件同实施案例1~6的Cu2O/SiO2-Al2O3气凝胶，对模拟汽油中噻吩类硫化物进行穿透吸附实验。其穿透吸附实验操作同实施例1~6，吸附结果见表5。The silicon source is tetraethyl orthosilicate, the copper source is copper acetate, and the reduction temperatures are 100, 120, 1400, 160, 180, 200, and 220°C, and other conditions are the same as Cu 2 O/SiO 2 in Examples 1-6. - Al 2 O 3 aerogel, for breakthrough adsorption experiments on thiophene sulfides in simulated gasoline. The operation of the breakthrough adsorption experiment is the same as in Examples 1-6, and the adsorption results are shown in Table 5.
表5 不同Cu2O/SiO2-Al2O3气凝胶的还原温度对吸附模拟汽油中噻吩类硫化物的影响Table 5 Effect of reduction temperature of different Cu 2 O/SiO 2 -Al 2 O 3 aerogels on adsorption of thiophene sulfides in simulated gasoline
从表5可以看出，Cu2O/SiO2-Al2O3气凝胶随着还原温度的上升，Cu2O/SiO2-Al2O3对噻吩与苯并噻吩的穿透吸附容量随之先增后降。在还原温度为120℃时，噻吩与苯并噻吩的穿透吸附容量达到最大，因此优选还原温度为100~160℃。It can be seen from Table 5 that the breakthrough adsorption capacity of Cu 2 O/SiO 2 -Al 2 O 3 airgel for thiophene and benzothiophene increases with the increase of reduction temperature. Then first increase and then decrease. When the reduction temperature is 120°C, the breakthrough adsorption capacity of thiophene and benzothiophene reaches the maximum, so the preferred reduction temperature is 100-160°C.
实施案例22~26：不同还原时间对Cu2O/SiO2-Al2O3复合气凝胶吸附模拟汽油中噻吩类硫化物的影响Implementation Cases 22~26: Effects of Different Reduction Times on Cu 2 O/SiO 2 -Al 2 O 3 Composite Airgel Adsorption of Thiophene Sulfides in Simulated Gasoline
选用硅源为正硅酸乙酯、铜源为醋酸铜，还原时间分别为3 h、4 h、5 h、6 h、7 h，其他条件同实施案例1~6的Cu2O/SiO2-Al2O3复合气凝胶，对模拟汽油中噻吩类硫化物进行穿透吸附实验。其穿透吸附实验操作同实施例1~6，吸附结果见表6。The silicon source is tetraethyl orthosilicate, the copper source is copper acetate, the reduction time is 3 h, 4 h, 5 h, 6 h, 7 h, and other conditions are the same as Cu 2 O/SiO 2 in the implementation cases 1~6. -Al 2 O 3 composite aerogel, for breakthrough adsorption experiments on thiophene sulfides in simulated gasoline. The operation of the breakthrough adsorption experiment is the same as in Examples 1-6, and the adsorption results are shown in Table 6.
表6 不同还原时间对吸附模拟汽油中噻吩类硫化物的影响Table 6 Effects of different reduction times on adsorption of thiophene sulfides in simulated gasoline
从表6可以看出，随着还原时间的加长，噻吩与苯并噻吩的穿透吸附容量会先增后减，当还原时间增加到5 h时，对噻吩类硫化物的穿透吸附容量变最大大，因此优选还原时间为4~6 h。It can be seen from Table 6 that as the reduction time increases, the breakthrough adsorption capacity of thiophene and benzothiophene will first increase and then decrease. When the reduction time increases to 5 h, the breakthrough adsorption capacity of thiophene sulfides will change The maximum is large, so the preferred reduction time is 4~6 h.
实施案例26~30：不同空速对复合气凝胶吸附模拟汽油中噻吩类硫化物的影响Implementation Cases 26~30: Effects of Different Space Velocities on Composite Airgel Adsorption of Thiophene Sulfides in Simulated Gasoline
选用硅源为正硅酸乙酯、铜源为醋酸铜，穿透空速分别为1 h-1、3 h-1、5 h-1、8 h-1、10h-1，其他条件同实施案例1~6的Cu2O/SiO2-Al2O3复合气凝胶，对模拟汽油中噻吩类硫化物进行穿透吸附实验。其穿透吸附实验操作同实施例1~6，吸附结果见表7。The silicon source is tetraethyl orthosilicate, the copper source is copper acetate, and the penetration space velocity is 1 h -1 , 3 h -1 , 5 h -1 , 8 h -1 , 10h -1 , and other conditions are the same as the implementation Cu 2 O/SiO 2 -Al 2 O 3 composite aerogels from Cases 1 to 6 were used for penetration adsorption experiments on thiophene sulfides in simulated gasoline. The operation of the breakthrough adsorption experiment is the same as in Examples 1-6, and the adsorption results are shown in Table 7.
表7 不同空速对吸附模拟汽油中噻吩类硫化物的影响Table 7 Effects of different space velocities on adsorption of thiophene sulfides in simulated gasoline
从表7可以看出，空速的减小，噻吩与苯并噻吩的穿透吸附容量会逐渐增大，当空速减小到5 h-1之后，对噻吩类硫化物的穿透吸附容量变化不大，因此优选空速为1~5 h-1。It can be seen from Table 7 that the breakthrough adsorption capacity of thiophene and benzothiophene will gradually increase with the decrease of space velocity, and the breakthrough adsorption capacity of thiophene sulfides will change when the space velocity decreases to 5 h Not too big, so the preferred space velocity is 1~5 h -1 .
实施案例31~35：不同吸附温度对Cu2O/SiO2-Al2O3复合气凝胶吸附模拟汽油中噻吩类硫化物的影响Implementation Cases 31~35: Effects of Different Adsorption Temperatures on Cu 2 O/SiO 2 -Al 2 O 3 Composite Airgel Adsorption of Thiophene Sulfides in Simulated Gasoline
选用硅源为正硅酸乙酯、铜源为醋酸铜，吸附温度分别选为0℃、25℃、40℃、80℃、100℃，其他条件同实施案例1~6的Cu2O/SiO2-Al2O3复合气凝胶，对模拟汽油中噻吩类硫化物进行穿透吸附实验。穿透吸附实验操作同实施例1~6，吸附结果见表8。The silicon source is tetraethyl orthosilicate, the copper source is copper acetate, and the adsorption temperatures are respectively selected as 0°C, 25°C, 40°C, 80°C, and 100°C, and other conditions are the same as Cu 2 O/SiO in Examples 1-6. 2 -Al 2 O 3 composite aerogels for breakthrough adsorption experiments on thiophene sulfides in simulated gasoline. The operation of the breakthrough adsorption experiment was the same as in Examples 1-6, and the adsorption results are shown in Table 8.
表8 不同吸附温度对吸附模拟汽油中噻吩类硫化物的影响Table 8 Effects of different adsorption temperatures on the adsorption of thiophene sulfides in simulated gasoline
从表8可以看出，随着吸附温度的升高，噻吩与苯并噻吩的穿透吸附容量逐渐减小，在80℃之后，噻吩与苯并噻吩的吸附穿透容量比较小，表明在此温度下，被Cu2O/SiO2-Al2O3复合气凝胶吸附的噻吩与苯并噻吩已脱附。因此优先吸附温度为0~40℃。It can be seen from Table 8 that as the adsorption temperature increases, the breakthrough adsorption capacity of thiophene and benzothiophene decreases gradually. After 80 °C, the adsorption breakthrough capacity of thiophene and benzothiophene is relatively small, indicating that At high temperature, thiophene and benzothiophene adsorbed by Cu 2 O/SiO 2 -Al 2 O 3 composite airgel have been desorbed. Therefore, the preferred adsorption temperature is 0~40°C.
实施案例36~39：不同硫浓度对Cu2O/SiO2-Al2O3复合气凝胶吸附模拟汽油中噻吩类硫化物的影响Implementation Cases 36~39: Effects of Different Sulfur Concentrations on Cu 2 O/SiO 2 -Al 2 O 3 Composite Airgel Adsorption of Thiophene Sulfides in Simulated Gasoline
选用硅源为正硅酸乙酯、铜源为醋酸铜，进料模拟汽油中的噻吩或苯并噻吩的硫浓度分别为100ppm、500ppm、1000ppm、2000ppm，其他条件同实施案例1~6的Cu2O/SiO2-Al2O3复合气凝胶，进行穿透吸附实验。穿透吸附操作同实施例1~6，吸附结果见表9。The silicon source is tetraethyl orthosilicate, the copper source is copper acetate, and the sulfur concentration of thiophene or benzothiophene in the feed simulated gasoline is 100ppm, 500ppm, 1000ppm, 2000ppm respectively, and other conditions are the same as the Cu 2 O/SiO 2 -Al 2 O 3 composite aerogels for breakthrough adsorption experiments. The breakthrough adsorption operation is the same as in Examples 1-6, and the adsorption results are shown in Table 9.
表9 不同硫浓度对吸附模拟汽油中噻吩类硫化物的影响Table 9 Effects of different sulfur concentrations on adsorption of thiophene sulfides in simulated gasoline
从表9可以看出，模拟汽油中噻吩或苯并噻吩硫浓度的增大，Cu2O/SiO2-Al2O3复合气凝胶对噻吩与苯并噻吩穿透吸附容量呈下降的趋势，因此优选模拟汽油中噻吩或苯并噻吩硫浓度为100~500 ppm。It can be seen from Table 9 that the breakthrough adsorption capacity of Cu 2 O/SiO 2 -Al 2 O 3 composite aerogels for thiophene and benzothiophene decreased with the increase of thiophene or benzothiophene sulfur concentration in simulated gasoline , so it is preferred that the sulfur concentration of thiophene or benzothiophene in simulated gasoline is 100-500 ppm.
Claims (10)
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN201611160480.3A CN106590728B (en) | 2016-12-15 | 2016-12-15 | One kind is with Cu2O/SiO2-Al2O3The method that composite aerogel removes thiophene sulphur in fuel oil for adsorbent |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN201611160480.3A CN106590728B (en) | 2016-12-15 | 2016-12-15 | One kind is with Cu2O/SiO2-Al2O3The method that composite aerogel removes thiophene sulphur in fuel oil for adsorbent |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| CN106590728A true CN106590728A (en) | 2017-04-26 |
| CN106590728B CN106590728B (en) | 2018-06-29 |
Family
ID=58802615
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CN201611160480.3A Active CN106590728B (en) | 2016-12-15 | 2016-12-15 | One kind is with Cu2O/SiO2-Al2O3The method that composite aerogel removes thiophene sulphur in fuel oil for adsorbent |
Country Status (1)
| Country | Link |
|---|---|
| CN (1) | CN106590728B (en) |
Cited By (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN108192656A (en) * | 2017-12-26 | 2018-06-22 | 浙江工业大学 | The removal methods of thiophene sulphur in a kind of fuel oil |
| CN108311099A (en) * | 2018-01-16 | 2018-07-24 | 浙江工业大学 | Ag2O/SiO2-Al2O3The method that graphene oxide composite aerogel removes thiophene sulphur in fuel oil |
| CN108728156A (en) * | 2018-06-12 | 2018-11-02 | 浙江工业大学 | Cu2O/SiO2-Al2O3The method of thiophene-type sulfide in-GO composite aerogel adsorbing and removing fuel oil |
| CN109592703A (en) * | 2018-12-18 | 2019-04-09 | 浙江大学自贡创新中心 | A kind of CuO/Cu2O-La2O3The preparation method of multiphase complex sol |
| CN112473575A (en) * | 2020-11-19 | 2021-03-12 | 浙江工业大学 | CeO (CeO)2-Ag2O(PdO)/SiO2Preparation method and application of composite aerogel |
Citations (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN1206020A (en) * | 1997-07-21 | 1999-01-27 | 青岛海洋化工集团公司 | Silicon-aluminum gel particle product and production method thereof |
| EP1514917A1 (en) * | 2002-05-22 | 2005-03-16 | Japan Energy Corporation | Adsorption desulfurization agent for desulfurizing petroleum fraction and desulfurization method using the same |
| CN103007873A (en) * | 2013-01-15 | 2013-04-03 | 南通大学 | Adsorbent for gasoline desulfurization and preparation method as well as application thereof |
| CN105709685A (en) * | 2015-12-31 | 2016-06-29 | 浙江工业大学 | A method for removing thiophene sulfur in gasoline using SiO2-CoO composite airgel as an adsorbent |
| CN106111054A (en) * | 2016-07-07 | 2016-11-16 | 浙江工业大学 | A method for removing thiophene-like sulfur in fuel oil using SiO2/Cu2O composite airgel as an adsorbent |
-
2016
- 2016-12-15 CN CN201611160480.3A patent/CN106590728B/en active Active
Patent Citations (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN1206020A (en) * | 1997-07-21 | 1999-01-27 | 青岛海洋化工集团公司 | Silicon-aluminum gel particle product and production method thereof |
| EP1514917A1 (en) * | 2002-05-22 | 2005-03-16 | Japan Energy Corporation | Adsorption desulfurization agent for desulfurizing petroleum fraction and desulfurization method using the same |
| CN103007873A (en) * | 2013-01-15 | 2013-04-03 | 南通大学 | Adsorbent for gasoline desulfurization and preparation method as well as application thereof |
| CN105709685A (en) * | 2015-12-31 | 2016-06-29 | 浙江工业大学 | A method for removing thiophene sulfur in gasoline using SiO2-CoO composite airgel as an adsorbent |
| CN106111054A (en) * | 2016-07-07 | 2016-11-16 | 浙江工业大学 | A method for removing thiophene-like sulfur in fuel oil using SiO2/Cu2O composite airgel as an adsorbent |
Non-Patent Citations (1)
| Title |
|---|
| 薛鸿霏: "分子筛表面酸性调变及其对噻吩类含硫化合物吸附的影响", 《中国优秀硕士学位论文全文数据库 工程科技Ⅰ辑》 * |
Cited By (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN108192656A (en) * | 2017-12-26 | 2018-06-22 | 浙江工业大学 | The removal methods of thiophene sulphur in a kind of fuel oil |
| CN108311099A (en) * | 2018-01-16 | 2018-07-24 | 浙江工业大学 | Ag2O/SiO2-Al2O3The method that graphene oxide composite aerogel removes thiophene sulphur in fuel oil |
| CN108728156A (en) * | 2018-06-12 | 2018-11-02 | 浙江工业大学 | Cu2O/SiO2-Al2O3The method of thiophene-type sulfide in-GO composite aerogel adsorbing and removing fuel oil |
| CN109592703A (en) * | 2018-12-18 | 2019-04-09 | 浙江大学自贡创新中心 | A kind of CuO/Cu2O-La2O3The preparation method of multiphase complex sol |
| CN112473575A (en) * | 2020-11-19 | 2021-03-12 | 浙江工业大学 | CeO (CeO)2-Ag2O(PdO)/SiO2Preparation method and application of composite aerogel |
| CN112473575B (en) * | 2020-11-19 | 2023-09-19 | 浙江工业大学 | A preparation method and application of CeO2-Ag2O(PdO)/SiO2 composite aerogel |
Also Published As
| Publication number | Publication date |
|---|---|
| CN106590728B (en) | 2018-06-29 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| CN106118717B (en) | One kind is with Ag2O/SiO2Composite aerogel is the method that adsorbent removes thiophene sulphur in fuel oil | |
| CN106590728B (en) | One kind is with Cu2O/SiO2-Al2O3The method that composite aerogel removes thiophene sulphur in fuel oil for adsorbent | |
| CN112452262B (en) | Preparation method and application of dopamine/silicon dioxide composite aerogel | |
| CN106111054A (en) | A method for removing thiophene-like sulfur in fuel oil using SiO2/Cu2O composite airgel as an adsorbent | |
| CN107033946B (en) | One kind is with Cu2O/SiO2-TiO2Composite aerogel is the method that adsorbent removes thiophene sulphur in fuel oil | |
| CN101347718A (en) | A new type of spherical activated carbon and its application in the field of desulfurization | |
| CN105289476A (en) | Metal-modified 13X molecular sieve desulphurization adsorbent and its preparation method and use | |
| RU2482162C1 (en) | Method of deep oxidation-absorption desulphurisation of liquid hydrocarbon fuels, and sorbents for its implementation | |
| CN108893138B (en) | Method for removing thiophene sulfides from fuel oil by using Ag2O/SiO2-ZrO2 composite aerogel as adsorbent | |
| CN108342217A (en) | One kind is with Ag2O/SiO2Graphene oxide composite aerogel is the method that adsorbent removes thiophene sulphur in fuel oil | |
| CN108949220A (en) | One kind is with Pd (II)-SiO2Composite aerogel is the method that adsorbent removes thiophene-type sulfide in fuel oil | |
| CN105709685B (en) | One kind is with SiO2CoO composite aerogels are the method that adsorbent removes thiophene sulphur in gasoline | |
| CN108940186B (en) | Method for adsorption and removal of thiophene sulfides in fuel oil by Ag2O/SiO2-TiO2 composite aerogel | |
| CN110354812A (en) | With SiO2- MTES-APTES composite aerogel is the method that adsorbent removes thiophene-type sulfide in fuel oil | |
| CN104190352B (en) | A kind of adsorbent for removing sulfur-bearing, oxygen impurities in light hydrocarbon materials stream and preparation thereof, renovation process | |
| CN108192656A (en) | The removal methods of thiophene sulphur in a kind of fuel oil | |
| CN101434863B (en) | Oxidative desulfurization method for sulfur-containing diesel | |
| CN108311099A (en) | Ag2O/SiO2-Al2O3The method that graphene oxide composite aerogel removes thiophene sulphur in fuel oil | |
| CN103170305A (en) | Modified gasoline desulfurization adsorbent and preparation method thereof | |
| CN110354809B (en) | A method for removing thiophene sulfides in fuel oil by using SiO2-APTES-Ag composite aerogel as adsorbent | |
| CN105623711B (en) | One kind is with SiO2NiO composite aerogels are the new method of thiophene sulphur in adsorbent removing gasoline | |
| CN110317631A (en) | The removal methods of thiophene sulphur in a kind of fuel oil | |
| CN101798525B (en) | Oxidation sweetening method for diesel oil | |
| CN108854953B (en) | Method for adsorption and removal of thiophene sulfur in fuel oil by Ag2O/SiO2-TiO2-graphene oxide composite aerogel | |
| CN108728156A (en) | Cu2O/SiO2-Al2O3The method of thiophene-type sulfide in-GO composite aerogel adsorbing and removing fuel oil |
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 |