Method of preparing expoxidation catalysts
US-2015375200-A1 · Dec 31, 2015 · US
US10399069B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-10399069-B2 |
| Application number | US-201815888019-A |
| Country | US |
| Kind code | B2 |
| Filing date | Feb 3, 2018 |
| Priority date | Aug 3, 2015 |
| Publication date | Sep 3, 2019 |
| Grant date | Sep 3, 2019 |
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The present invention relates to a hydroisomerization and cracking catalyst for preparing biological aviation kerosene from castor oil as well as a preparation method and an application thereof. The catalyst takes a Al-modified titanium silicate molecular sieve (TS-1) as a carrier, and takes Ni x W and Ni x Mo as active components, wherein x is the atomic ratio of Ni to W or Ni to Mo, and x=5-10, wherein the mass of the active components accounts for 5-30% of the total mass of the catalyst; the molar ratio of Si:Ti in the Al-modified titanium silicate molecular sieve is 50-100, and the molar ratio of Si:Al is 50-100.
Opening claim text (preview).
We claim: 1. A preparation method of a hydroisomerization and cracking catalyst for preparing biological aviation kerosene from castor oil, the catalyst comprising titanium silicate molecular sieve (TS-1) as a carrier, and NixW and NixMo as active components, wherein x is an atomic ratio of Ni to W or Ni to Mo, and x=5-10, Al is removed partially from the carrier, and a mass of the active components accounts for 5-30% of a total mass of the catalyst, the preparation method comprising following steps: 1) thoroughly stirring and mixing an aqueous solution of tetrapropylammonium hydroxide with a tetraethoxysilane solution at a temperature of 40-55° C. for 0.5-2 h, then adding an isopropanol solution of tetrabutyl titanate to obtain a mixed solution, and then adding aluminium isopropoxide and continuously stirring for 1-3 h; 2) heating, stirring and refluxing the above mixed solution in a water bath with a constant temperature of 75-85° C. for 1-3 h to remove the isopropanol from the solution, and then complementing the mass of the solution obtained after refluxing to the value before heating, stirring and refluxing by using deionized water; 3) transferring the above solution into a high pressure reaction kettle to conduct aging at 95-105° C. for 4-6 h, then heating to 150-180° C. to conduct crystallization for 6-36 h to obtain a sample, taking out and washing the sample with deionized water until neutral, calcining in a muffle furnace at 500-550° C. for 4-6 h after drying, cooling to room temperature and then placing into an HCl solution of 0.5 mol/L, and heating, stirring and refluxing at 50-60° C. for 1-5 h; 4) separating the sample through suction filtration, washing with deionized water until neutral, and after drying, calcining at 500-550° C. for 2-4 h under a nitrogen atmosphere to obtain the carrier; 5) sequentially adding nickel nitrate, and ammonium metatungstate, or adding nickel nitrate an ammonium molybdate, into an aqueous solution of urea according to a ratio under room-temperature stirring conditions, stirring for 0.5-1 h until completely dissolved, then adding the carrier and stirring for at least 2 h, and drying the mixture in a rotary evaporator at 80-90° C. to obtain solid powder; and 6) calcining the solid powder in an air atmosphere at 550-600° C. for at least 2 h, then reducing at 550-600° C. at a hydrogen flow rate of 200-300 mL/min for at least 3 h, cooling to room temperature, and then passivating with O 2 /N 2 passivating gases at a volume ratio of 1% for 3 hours to obtain the desired catalyst. 2. The method according to claim 1 , wherein a ratio of materials in steps 1) to 2) is SiO 2 :TiO 2 :TPAOH:aluminium isopropoxide:isopropanol:H2O=1:(0.01-0.02):(0.1-0.4):(0.01-0.02):(0.1-0.5):(20-100). 3. The method according to claim 1 , wherein an added amount of the urea in step 5) is 2-5% of the mass of the carrier. 4. The method according to claim 1 , wherein an added amount of the urea in step 5) is 2-3% of the mass of the carrier.
including cracking steps and other hydrotreatment steps · CPC title
containing crystalline aluminosilicates, e.g. molecular sieves · CPC title
Processes, in general, for preparing catalysts; Processes, in general, for activation of catalysts · CPC title
and nickel · CPC title
Chromium, molybdenum or tungsten · CPC title
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