Hydrocarbon oil desulfurization catalyst containing FAU-structure and/or BEA-structure molecular sieve, preparation method of hydrocarbon oil desulfurization catalyst and process for hydrocarbon oil desulfurization
A desulfurization catalyst and molecular sieve technology, which is applied in the field of hydrocarbon oil desulfurization, can solve the problems of easy wear of catalysts and increase operating costs, and achieve the effects of good anti-wear performance, reduced operating costs and high gasoline octane number.
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[0036] The present invention also provides the preparation method of the hydrocarbon oil desulfurization catalyst provided by the present invention, the preparation method comprising: a, the sulfur-storing metal oxide and / or the precursor of the sulfur-storing metal oxide, the precursor of the zirconia binder, Boron nitride, molecular sieves with FAU structure and / or molecular sieves with BEA structure, water, and acidic liquid are mixed to obtain carrier slurry; wherein, the pH value of the carrier slurry is 1-5; b. The obtained carrier slurry is spray-dried and formed in sequence , the first drying and the first roasting to obtain the catalyst carrier; c, after introducing the precursor of the metal promoter into the catalyst carrier, carry out the second drying and the second roasting successively; optional d, the product obtained in step c in a hydrogen-containing atmosphere Reduction treatment is carried out under the atmosphere; a hydrocarbon oil desulfurization catalyst ...
Embodiment approach
[0047] One embodiment, the present invention specifically includes the following solutions:
[0048] 1. A desulfurization catalyst comprising:
[0049] 1) Sulfur-storage metal oxides, wherein the sulfur-storage metal is selected from one or more of the metals of Group IIB of the Periodic Table of the Elements, the metals of Group VB of the Periodic Table of the Elements, and the metals of Group VIB of the Periodic Table of the Elements, preferably selected from One or more of zinc, cadmium, niobium, tantalum, chromium, molybdenum, tungsten and vanadium, more preferably one or more selected from zinc, molybdenum and vanadium, more preferably zinc;
[0050] 2) Inorganic binder, preferably zirconia;
[0051] 3) The carrier component is boron nitride (preferably hexagonal phase boron nitride) or said boron nitride and oxides, nitrides, carbides, oxynitrides, carbonitrides, carbon oxides selected from element A and a combination of one or more of oxycarbonitride, wherein the elem...
Embodiment 1
[0099] 1.91kg of zirconium tetrachloride (Beijing Chemical Plant, analytically pure, 99% by weight) was slowly added to 3.0kg of deionized water, and 4.6kg of 5% by weight of nitric acid solution was added, slowly stirred to avoid the precipitation of zirconia crystals, and obtained Light yellow transparent zirconium sol pH=2.1;
[0100] With 4.43kg of zinc oxide powder (Headhorse company, purity 99.7% by weight), 0.88kg of Hβ molecular sieve (Sinopec Catalyst Qilu Branch, containing dry basis 0.70kg, SiO 2 :Al 2 o 3 The molar ratio is 8), 2.06kg of hexagonal boron nitride (purity>99.0%, Qinhuangdao Yinuo High-tech Material Development Co., Ltd.) and 6.57kg of deionized water are mixed, and after stirring for 30 minutes, zinc oxide, Hβ molecular sieve and hexagonal boron nitride are obtained. A mixed slurry of boron nitride; then adding the above-mentioned zirconium sol, mixing and stirring for 1 hour to obtain a carrier slurry;
[0101] The resulting carrier slurry was use...
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