CN104368393A - Alumina product, its preparation method, and catalyst prepared with product as carrier - Google Patents
Alumina product, its preparation method, and catalyst prepared with product as carrier Download PDFInfo
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- CN104368393A CN104368393A CN201310357375.9A CN201310357375A CN104368393A CN 104368393 A CN104368393 A CN 104368393A CN 201310357375 A CN201310357375 A CN 201310357375A CN 104368393 A CN104368393 A CN 104368393A
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Abstract
The invention relates to an alumina product, its preparation method, and a catalyst prepared with the product as a carrier. A result of characterization of the catalyst through a mercury intrusion technology shows that the pore volume of the product is 0.3-0.8ml/g, the specific surface area is 70-220m<2>/g, the pore volume of pores with the diameter of 6-10nm accounts for 8-25% of the total pore volume, and the pore volume of pores with the diameter of 85-160nm accounts for 40-75% of the total pore volume. The alumina product can e used as a routine adsorbent, and can also be used in a filler of a reaction apparatus as a filling material. The product is especially suitable for preparing hydrogenation activity protection agents and other catalysts as a carrier when the product is used to prepare hydrogenation catalysts as a carrier.
Description
Technical field
The catalyst that the present invention relates to a kind of aluminium oxide article shaped and preparation method thereof and prepared as carrier by this article shaped.
Background technology
Along with crude quality is deteriorated, in crude oil, the impurity content such as colloid, asphalitine and organo-metallic compound increases, and the existence of these impurity is easy to the quick decline so that the inactivation that cause catalyst activity.The effective ways addressed this problem are the protective agents in the filling of hydrogenation catalyst bed top with hydrogenation activity.Have and hold metal and hold charcoal ability strong compared with the hydrogenation protecting catalyst of large pore volume and bore dia, the effect of protection downstream hydrogenation host can be played, extend the service life of host.
In prior art about the example of hydrogenation protecting catalyst and preparation thereof as:
CN200610113493.5 discloses a kind of hydrogenation protecting agent and preparation thereof; this protective agent contains the heat-resistant inorganic oxide of one or more porous; it is characterized in that; the total pore volume of described protective agent be 0.3-1.5 millimeter/gram; wherein containing grade macropore; grade macropore bore dia is 0.1 ~ 1.5 micron, and grade macropore pore volume is 0.05 ~ 0.7 ml/g.The preparation method of described hydrogenation protecting agent; comprise the precursor of the heat-resistant inorganic oxide of one or more porous and/or the heat-resistant inorganic oxide of porous is mixed with at least one organic matter, shaping, dry and roasting; wherein, described organic compound is fusing point between 30 ~ 200 DEG C, particle diameter 0.3 ~ 2.5 millimeter and water-fast solid particle.
CN201010220850.4 discloses the protectant preparation method of a kind of hydrotreatment.In the method, alumina support is prepared by the different boehmite dry glue powder kneading method of employing two kinds, then supported active metals; Wherein the first crystallization degree of pseudo-boehmite is relatively little, pore volume is large, the hole of bore dia 30nm ~ 100nm can be provided, the second crystallization degree of pseudo-boehmite is relatively high, can provide micron-sized hole, again because its acidity indexes is high, extremely hard bulk is presented after drying, after being pulverized, 100% by 50 orders, not only can increase the quantity of micrometer grade hole, also can improve the intensity of catalyst carrier.By adjustment mixed proportion between the two, the hydrotreatment protective agent that intensity is high, bulk density is large, pore volume is large and wear rate is low can be made.
CN98111379.6 discloses hydrogenation protecting catalyst and preparation method thereof, and this catalyst carrier is ultra-large aperture, and aperture is the bimodal hole of 0.1-30 μm, and catalyst pore volume is 0.1-0.8ml/g, specific surface 0.1-20m
2/ g, containing group vib metallic element 6.65m%-20.0m and/or VIII race's metallic element 8.71% ,-26.13m%.Preparation method adopts particle to pile up legal system for alumina support, then adopts containing molybdenum solution and solution containing nickel equivalent impregnation, the catalyst after dipping at 100-120 DEG C of dry 2-5h, at 500-550 DEG C of roasting 2-5h.
CN00110019.X discloses a kind of Hydrogenation active protective agent and preparation method thereof, simultaneously containing γ mono-aluminium oxide and δ-aluminium oxide in protective agent used carrier; Containing group vib metal oxide 3-22m% and VIII family metal oxide 0.5-5m% in protective agent, containing IA family metal oxide 0-2m%, phosphorous 0-3m%, specific surface 100-250m
2/ g.Pore volume 0.4-0.8ml/g.
CN200910206230.2 discloses a kind of hydrotreating guard catalyst for residual oil and application thereof.This catalyst pore volume is large, and aperture is large, and porosity is high, reasonable pore distribution, and outer surface orifice is comparatively large, and duct penetrability is good, and more than 1000nm contains more than 36% in duct.In particular in residue fixed-bed hydrogenation method, the metal deviate from can be made to homogeneously precipitate in whole beds, impurity vanadium and calcium can be deposited in inside, duct, improve the utilization rate of hole, keep long-term operation.
Problem during above-mentioned prior art uses for hydrogenation protecting catalyst, gives various different solution.Be not difficult to find out, carrier hole character wherein directly decides (comprising pore volume, aperture, the character such as pore size distribution) performance of this type of catalyst.
Summary of the invention
The technical problem to be solved in the present invention is to provide a kind of aluminium oxide article shaped with bimodal pore distribution newly and preparation method thereof, and the hydrogenation protecting catalyst adopting this carrier to prepare.
The content that the present invention relates to comprises:
1, an aluminium oxide article shaped, characterize with mercury injection method, the pore volume of described article shaped is 0.3-0.8 ml/g, and specific area is 70-220 rice
2/ gram, wherein, diameter is the 8-25% that the pore volume in 6-10nm hole accounts for total pore volume, and diameter is the 40-75% that the pore volume in 85-160nm hole accounts for total pore volume.
2, the aluminium oxide article shaped according to 1, is characterized in that, the pore volume of described article shaped is 0.4-0.7 ml/g, and specific area is 80-210 rice
2/ gram, wherein, diameter is the 10-20% that the pore volume in 6-10nm hole accounts for total pore volume, and diameter is the 45-70% that the pore volume in 85-160nm hole accounts for total pore volume.
3, the aluminium oxide article shaped according to 1, it is characterized in that, containing one or more adjuvant components be selected from IA and IIA in described aluminium oxide article shaped, with oxide basis and with described article shaped total amount for benchmark, the content of described adjuvant component is less than 10 % by weight.
4, the aluminium oxide article shaped according to 3, it is characterized in that, described IA is selected from one or more in lithium, sodium and potassium, and described IIA is selected from one or more in magnesium, calcium and barium, with oxide basis and with described article shaped total amount for benchmark, the content of described adjuvant component is 2.5-5.5 % by weight.
The preparation method of the aluminium oxide article shaped 5, according to 1, comprise a kind of hydrated alumina is mixed with a kind of Alpha-alumina, shaping, dry and roasting, sintering temperature is 750-1000 DEG C, roasting time is 1-10 hour, wherein, in the mixing ratio of the hydrated alumina of butt and Alpha-alumina for 15-70:30-85, the pore volume of described hydrated alumina is 0.3-1.1 ml/g, and specific surface is 150-350 rice
2/ gram, most probable bore dia 5-20nm.
6, the method according to 5, it is characterized in that, described sintering temperature is 800-950 DEG C, roasting time is 2-8 hour, wherein, in the mixing ratio of the hydrated alumina of butt and Alpha-alumina for 30-70:30-70, the pore volume of described hydrated alumina is 0.35-1 ml/g, and specific surface is 150-300 rice
2/ gram, most probable bore dia 6-15nm.
7, the method according to 5 or 6, is characterized in that, described hydrated alumina is selected from boehmite.
8, the method according to 5, is characterized in that, comprise the step introducing one or more adjuvant components be selected from IA and IIA, with oxide basis and with described article shaped total amount for benchmark, the introduction volume of described adjuvant component is less than 10 % by weight.
9, the method according to 8, it is characterized in that, described IA is selected from one or more in lithium, sodium and potassium, and described IIA is selected from one or more in magnesium, calcium and barium, with oxide basis and with the described article shaped total amount introduction volume that is adjuvant component described in benchmark for 2.5-5.5 % by weight.
10, a hydrogenation catalyst, containing aluminium oxide shaping carrier, is characterized in that, described carrier is the article shaped in claim 1-4 described in any one.
11, the hydrogenation catalyst according to 10, it is characterized in that, hydrogenation active metals component in described catalyst is selected from the metal component of at least one the VIIIth race and at least one group VIB, with oxide basis and with described catalyst for benchmark, the content of described metal component of group VIII is for being greater than 0 to being less than or equal to 8 % by weight, and the content of described metal component of group VIB is for being greater than 0 to being less than or equal to 10 % by weight.
12, the catalyst according to 11, it is characterized in that, described metal component of group VIII is selected from nickel and/or cobalt, described metal component of group VIB is selected from molybdenum and/or tungsten, with oxide basis and with described catalyst for benchmark, the content of described metal component of group VIII is 0.2 ~ 4 % by weight, and the content of described metal component of group VIB is 0.5 ~ 8 % by weight.
The preparation method of aluminium oxide article shaped provided by the invention comprise hydrated alumina is mixed with Alpha-alumina, shaping, drying roasting obtains.
Wherein, described Alpha-alumina can be commercially available commodity (commodity alpha-alumina), also can be obtained through high-temperature roasting by hydrated alumina (alumina hydrate powder).Under being enough to that hydrated alumina roasting phase transformation is converted into the condition of Alpha-alumina, this process can adopt arbitrary existing method to realize, and does not limit this present invention.
It is 0.35-1.1 ml/g that described hydrated alumina is selected from arbitrary pore volume, and be preferably 0.35-1.0 ml/g, specific surface is 150-350 rice
2/ gram, be preferably 150-300 rice
2/ gram, most probable bore dia is 5-20nm, is preferably 6-15nm, the more preferably hydrated alumina of 6-10nm; Described hydrated alumina is preferably the hydrated alumina containing boehmite.Here, the pore volume of described hydrated alumina, specific area and can and aperture, be that described hydrated alumina after 4 hours in 600 DEG C of roastings, is characterized by BET nitrogen absorption under low temperature and obtains.
In the present invention, described hydrated alumina adopts conventional method with mixing of Alpha-alumina, and meet in the mixing ratio of the hydrated alumina of butt and Alpha-alumina for 15-70:30-85(wherein, 15-70 refers to that the hydrated alumina (in butt) of every hundred parts is with the mixture of Alpha-alumina, and the value of hydrated alumina number changes between 15-70; 30-85 refers to that the hydrated alumina (in butt) of every hundred parts is with the mixture of Alpha-alumina, and the value of Alpha-alumina number changes between 30-85), be preferably 30-70:30-70.
According to article shaped provided by the invention, can be made into the various shape being easy to operate depending on different requirement, such as spherical, cellular, nest like, tablet or bar shaped (clover, butterfly, cylindrical etc.).Shapingly can to carry out according to a conventional method, such as, a kind of method in spin, compressing tablet and extruded moulding or the combination of several method.When shaping, such as extruded moulding, for ensureing described shapingly to carry out smoothly, can add in described material to be formed water, extrusion aid and/or adhesive, containing or not containing expanding agent, then extrusion molding, carry out drying also roasting afterwards.The kind of described extrusion aid, peptizing agent and consumption are conventionally known to one of skill in the art, such as common extrusion aid can be selected from one or more in sesbania powder, methylcellulose, starch, polyvinyl alcohol, PVOH, described peptizing agent can be inorganic acid and/or organic acid, and described expanding agent can be one or more in starch, synthetic cellulose, polymeric alcohol and surfactant.Synthetic cellulose is wherein preferably one or more in CMC, methylcellulose, ethyl cellulose, hydroxyl fiber fat alcohol polyethylene ether, polymeric alcohol is preferably one or more in polyethylene glycol, poly-propyl alcohol, polyvinyl alcohol, one or more in the propenyl copolymer that surfactant is preferably fat alcohol polyethylene ether, fatty alkanol amide and derivative thereof, molecular weight is 200-10000 and maleic acid copolymer.
In the present invention, the drying of described article shaped is conventional method and condition.The method of described roasting is conventional method, and it is 600-1000 DEG C that the condition of described roasting preferably includes sintering temperature, and roasting time is 1-10 hour, and it is 700-950 DEG C that the condition of preferably roasting further comprises sintering temperature, and roasting time is 2-8 hour.
According in aluminium oxide article shaped provided by the invention, can containing one or more adjuvant components be selected from IA and IIA, with described article shaped total amount for benchmark, the content of described adjuvant component is less than 10 % by weight with oxide basis, is preferably 2.5 % by weight-5.5 % by weight.Wherein, one or more preferably in lithium, sodium and potassium of described IA, further preferred sodium and/or potassium, one or more preferably in magnesium, calcium and barium of described IIA, further preferably magnesium and/or calcium.
When also comprising adjuvant component in described article shaped, the preparation method of described article shaped comprises the step introducing adjuvant component component, with oxide basis and with described article shaped total amount for benchmark, the introduction volume of described adjuvant component is less than 10 % by weight, is preferably 2.5-5.5 % by weight.
The introducing method of described adjuvant component is conventional method, such as, can be directly the compound containing adjuvant component of aequum is mixed in the mixed process of aforesaid hydrated alumina and Alpha-alumina, maybe be mixed with the aqueous solution by containing the compound of adjuvant component, afterwards this aqueous solution be mixed in the mixed process of aforesaid hydrated alumina and Alpha-alumina.
Concrete prepare in the embodiment of carrier at one, the method introduced in the mixture of described hydrated alumina and Alpha-alumina containing the compound of adjuvant component is that the compound containing adjuvant component is mixed with the aqueous solution, this aqueous solution is mixed into while described hydrated alumina mixes with Alpha-alumina or again this aqueous solution is mixed into after described hydrated alumina mixes with Alpha-alumina, aftershaping, dry and roasting.The compound of described alkali metal containing can be one or more in arbitrary alkali-metal water soluble compound.Such as, one or more in the water-soluble inorganic salt of alkali-metal water-soluble inorganic salt and alkaline-earth metal.
The micropore character of aluminium oxide article shaped provided by the invention be 6-10nm and diameter is 85-160nm two place at diameter is obvious bimodal distribution.The aluminium oxide article shaped with attribute of the present invention, except can be used as common adsorbents and using, can also use as the filler of filler for reaction unit.When this article shaped is prepared hydrogenation class catalyst as carrier, the carrier be particularly suitable as catalyst such as Hydrogenation active protective agent uses.
According to hydrogenation protecting catalyst provided by the invention; hydrogenation active metals component wherein and content thereof are the hydrogenation active metals component and content that hydrogenation protecting catalyst is conventional; such as, described hydrogenation active metals component is selected from least one the VIIIth race's non-noble metal components and at least one group vib metal component.The metal component of preferred VIIIth race is nickel and/or cobalt, the metal component of preferred group vib is molybdenum and/or tungsten, with oxide basis and with described catalyst for benchmark, the content of described group VIII metal is 0.1 ~ 8 % by weight, be preferably 0.2 ~ 4 % by weight, the content of described group vib metal component is 0.5 ~ 10 % by weight, is preferably 0.5 ~ 8 % by weight.
Except described carrier; the preparation method of described hydrogenation protecting catalyst comprises the step introducing hydrogenation active metals component on described carrier, and hydrogenation active metals component is wherein selected from least one the VIIIth race's base metal and the combination being selected from least one group vib metal.The metal component of preferred group vib is molybdenum and/or tungsten, with oxide basis and with described catalyst for benchmark, the introduction volume of described group vib metal component makes the content of group vib metal component in final catalyst for being greater than 0 to being less than or equal to 10 % by weight, be preferably 0.5 ~ 8 % by weight, the introduction volume of described metal component of group VIII makes the content of metal component of group VIII in final catalyst for being greater than 0 to being less than or equal to 8 % by weight, is preferably 0.2 ~ 4 % by weight.
What on described carrier, introduce hydrogenation active metals component can be any means that those skilled in the art inform, such as, by carrier described in the solution impregnation with the compound containing described hydrogenation active metals component, the step of drying, roasting or not roasting can be carried out afterwards.
In the present invention, the described compound containing group vib metal be selected from they soluble compound in one or more.Such as, the compound containing molybdenum can be one or more in molybdenum oxide, molybdate, paramolybdate, preferably molybdenum oxide, ammonium molybdate, ammonium paramolybdate wherein; Tungstenic compound is selected from one or more in tungstates, metatungstate, ethyl metatungstate, preferably ammonium metatungstate, ethyl ammonium metatungstate wherein.
The described compound containing group VIII metal be selected from they soluble compound in one or more.Such as, the compound containing cobalt can be one or more in cobalt nitrate, cobalt acetate, basic cobaltous carbonate, cobalt chloride, is preferably cobalt nitrate, basic cobaltous carbonate; Nickel compound containing can be one or more in nickel nitrate, nickel acetate, basic nickel carbonate, nickel chloride, is preferably nickel nitrate, basic nickel carbonate.
According to the present invention, the solution of the compound containing described active component prepared by the various solvents that this area can be adopted to commonly use, as long as described compound can be dissolved in described solvent, forms the solution of stable homogeneous.Such as: described solvent can for water or carbon number be 1 ~ 5 alcohol (as: ethanol), be preferably water and/or ethanol, be more preferably water.
The method of described dipping can be the conventional various dipping methods in this area, such as, can be the saturated infusion process in hole.The present invention was not particularly limited for the time of described dipping and the number of times of dipping, as long as can guarantee that the amount with the active component of catalytic action on the catalyst that finally obtains meets concrete instructions for use.Usually, the time of described dipping can be 0.5 ~ 12 hour.
According to the present invention, the carrier for compound load being had described hydrogenation active metals component carries out dry method and condition is not particularly limited.Usually, the temperature of described drying can be 80 ~ 350 DEG C, is preferably 100 ~ 300 DEG C; The time of described drying can be 0.5 ~ 24 hour, is preferably 1 ~ 12 hour.
When catalyst after drying needs to carry out roasting, the present invention is not particularly limited described method of roasting and condition, can be conventional method and the condition of this area.Usually, the temperature of described roasting can be 350 ~ 650 DEG C, is preferably 400 ~ 500 DEG C; The time of described roasting can be 0.2 ~ 12 hour, is preferably 1 ~ 10 hour.Described roasting can be carried out in oxygen-containing atmosphere, also can carry out in an inert atmosphere.
According to catalyst provided by the invention, can also not affect containing any the adjuvant component that the performance that the invention provides catalyst maybe can improve catalyst performance provided by the invention.As contained the components such as phosphorus, be benchmark in element and with catalyst, the content of described auxiliary agent is no more than 10 % by weight, is preferably 0.5-5 % by weight.
When in described catalyst also containing when being selected from the components such as phosphorus, also comprise the step introducing the components such as phosphorus, the introducing method of the components such as described phosphorus can pass through number of ways, preferred method be by the compound containing described auxiliary agent be mixed with containing the compound of hydrogenation active metals component after mixed solution with described carrier contact; Can also be by after independent for the compound containing auxiliary agent obtain solution with described carrier contact and roasting.When auxiliary agent and hydrogenation active metals introduce described carrier respectively, preferably first use containing auxiliary compound solution and described carrier contact and roasting, contact with the solution of the compound containing hydrogenation active metals component more afterwards, such as by the method for dipping, described sintering temperature is 250-600 DEG C, be preferably 350-500 DEG C, roasting time is 2-8 hour, is preferably 3-6 hour.
Protective agent provided by the invention is applicable to the protective agent carrying out adding man-hour as heavier hydrocarbon feeds; the heavy raw oil being particularly useful for doing high-sulfur height nitrogen height tenor inferior also comprises the protective agent of decompression residuum; this protective agent is loaded on hydrogenation catalyst top; effectively can solve the fouling of industrial hydrogenation plant bed, blocking, pressure drop excessive and be forced to the problem of stopping work, extend the service life of downstream hydrogenation catalyst.
Detailed description of the invention
The present invention is described further for example below.
Agents useful for same in example, except as expressly described, is chemically pure reagent.
Pressure mercury method (RIPP149-90) measures (Yang Cuiding etc., Petrochemical Engineering Analysis method, publishing house of the academy of sciences, the 1990, the 421-423 pages) such as the specific area of aluminium oxide shaping carrier, pore volume and pore size distributions.
BET nitrogen absorption under low temperature method (RIPP151-90) measures specific area, the pore volume and pore size distribution etc. (Yang Cuiding etc., Petrochemical Engineering Analysis method, publishing house of the academy of sciences, the 1990, the 424-426 page) of hydrated alumina.
Butt assay method, for getting appropriate amount of sample, in 600 DEG C of roasting temperature 3h, afterwards, calculates the mass percent of sample before sample and roasting after roasting, is the butt of this sample.
XRF method (RIPP132-90) is adopted to measure the content (Yang Cuiding etc., Petrochemical Engineering Analysis method, publishing house of the academy of sciences, 1990,371-375 page) of adjuvant component and hydrogenation active metals component in catalyst.
Embodiment 1
(be available commercially from Yantai Heng Hui Chemical Co., Ltd., butt is 72 % by weight to take 200g hydrated alumina.Pore volume is 0.50 ml/g, and specific area is 290 meters
2/ gram, most probable bore dia is 7nm), 70 grams of alpha-aluminas (being formed for 6 hours by the hydrated alumina used in the present embodiment roasting at 1400 DEG C), 9 grams of sesbania powder mixing, add 230 milliliters, water, after mixing afterwards, kneading in double screw banded extruder is also extruded with the cylindrical orifice plate of φ 2.0mm, afterwards, wet bar through 120 DEG C of dryings after 4 hours in 850 DEG C of roastings 2 hours, obtain carrier T-1 of the present invention.Measure the specific surface of carrier T-1, can a few aperture, pore volume, pore size distribution, the results are shown in Table 1.
Embodiment 2
(be available commercially from the neat cyclopentadienyl catalyst factory in Zibo, butt is 68 % by weight to take 180g dry glue powder.Pore volume is 0.55 ml/g, and specific area is 278 meters
2/ gram, most probable bore dia is 8nm), 120 grams of alpha-aluminas (being available commercially from Beijing Shun Chuan Environmental Protection Technology Co., Ltd), 9 grams of sesbania powder mixing, add the aqueous solution 205 milliliters containing 11.0 grams, potassium nitrate afterwards, after mixing, in double screw banded extruder, kneading is also extruded with the cylindrical orifice plate of φ 2.0mm, afterwards, wet bar through 120 DEG C of dryings after 4 hours in 850 DEG C of roastings 2 hours, obtain carrier T-2 of the present invention.Measure the specific surface of carrier T-2, can a few aperture, pore volume, pore size distribution, the results are shown in Table 1.
Embodiment 3
(be available commercially from Yantai Heng Hui Chemical Co., Ltd., butt is 72 % by weight to take 150g dry glue powder.Pore volume is 0.50 ml/g, and specific area is 255 meters
2/ gram, most probable bore dia is 9nm), 150 grams of alpha-aluminas (with embodiment 2), 9 grams of sesbania powder, 9 grams of methylcellulose and 7.0 grams of calcium carbonate (Chemical Reagent Co., Ltd., Sinopharm Group) mixing, add 200 ml waters afterwards, shaping according to roller forming method after mixing, obtaining particle diameter is 5.5-6.5mm spheric granules.Wet bar through 120 DEG C of dryings after 4 hours in 800 DEG C of roastings 2 hours, obtain carrier T-3 of the present invention.Measure the specific surface of carrier T-3, can a few aperture, pore volume, pore size distribution, the results are shown in Table 1.
Embodiment 4
Take 260g dry glue powder (with embodiment 1), 140 grams of alpha-aluminas (with embodiment 1), 9 grams of sesbania powder, 9 grams of methylcellulose mixing, add the aqueous solution 205 milliliters containing lithium nitrate 16.5 grams afterwards, after mixing in double screw banded extruder kneading extruding with the cylindrical orifice plate of φ 2.0mm, wet bar through 120 DEG C of dryings after 4 hours in 800 DEG C of roastings 2 hours, obtain carrier T-4 of the present invention.Measure the specific surface of carrier T-4, can a few aperture, pore volume, the results are shown in Table 1.
Embodiment 5
Take 260g dry glue powder (with embodiment 2), 140 grams of alpha-aluminas (with embodiment 1), 9 grams of sesbania powder, 9 grams of methylcellulose and 9 grams of methylcellulose and 7.8 grams of magnesium hydroxides (Chemical Reagent Co., Ltd., Sinopharm Group) mixing, add the aqueous solution 200 milliliters afterwards, mix rear extruded moulding, wet bar through 120 DEG C of dryings after 4 hours in 800 DEG C of roastings 2 hours, obtain carrier T-4 of the present invention.Measure the specific surface of carrier T-4, can a few aperture, pore volume, the results are shown in Table 1.
Comparative example 1
Take 300 grams of dry glue powders (with embodiment 3), 9 grams of sesbania powder, after mixing, add the solution 200 milliliters of mixed-formings containing 12 grams, nitric acid, wet bar through 120 DEG C of dryings after 4 hours in 850 DEG C of roastings 2 hours, obtain carrier D-1.Measure the specific surface of carrier D-1, can a few aperture, pore volume, the results are shown in Table 1.
Comparative example 2
(be available commercially from Chang Ling oil refining catalyst factory, butt is 65 % by weight to take 300 grams of dry glue powders.Pore volume is 0.8 ml/g, and specific area is 320 meters
2/ gram, most probable bore dia is 9nm), 9 grams of sesbania powder and magnesium nitrate (AlfaAesar (Tianjin) Chemical Co., Ltd.) 8 grams, the solution 220 milliliters of mixed-formings containing 12 grams, nitric acid are added after mixing, wet bar through 120 DEG C of dryings after 4 hours in 850 DEG C of roastings 2 hours, obtain carrier D-2.Measure the specific surface of carrier D-2, can a few aperture, pore volume, the results are shown in Table 1.
Comparative example 3
((be available commercially from Chang Ling oil refining catalyst factory, butt is 65 % by weight to take dry glue powder.Pore volume is 0.8 ml/g, and specific area is 290 meters
2/ gram, most probable bore dia is 10nm)) 300 grams, add carbon black powder 24 grams, the mixing of 12 grams, sesbania powder, the aqueous solution 260 milliliters, kneading 15 minutes, double screw banded extruder is extruded into the butterfly bar of Φ 1.5mm, wet bar through 120 DEG C of dryings after 4 hours in 950 DEG C of roastings 2 hours, obtain carrier D-3.Measure the specific surface of carrier D-3, can a few aperture, pore volume, the results are shown in Table 1.
Comparative example 4
(be available commercially from Chang Ling oil refining catalyst factory, butt is 65 % by weight to take 300 grams of dry glue powders.Pore volume is 0.65 ml/g, and specific area is 288 meters
2/ gram, most probable bore dia is 9nm), 9 grams of sesbania powder, add the solution 360 milliliters of mixed-formings containing 12 grams, potassium nitrate after mixing, wet bar through 120 DEG C of dryings after 4 hours in 950 DEG C of roastings 2 hours, obtain carrier D-4.Measure the specific surface of carrier D-4, can a few aperture, pore volume, the results are shown in Table 1.
Table 1
The result that table 1 provides shows, alumina support provided by the invention is except having larger most probable pore size, and pore size distribution mainly concentrates on bore dia is 6-10nm and 85-160nm, be namely 6-10nm and 85-160nm scope at bore dia is obvious bimodal distribution.
Embodiment 6
Get carrier 100 grams of rear drying and roastings of T1 dipping, in saturated leaching mode with containing 1.2g molybdenum oxide (containing MoO
399.9%) and the solution 82 milliliters dipping of 0.7g nickel nitrate (containing NiO25%), 120 DEG C of dryings 4 hours after dipping, 420 DEG C of roastings 3 hours guard catalyst TC-1 of the present invention.Wherein, the content of hydrogenation active metals component lists in table 2.
Embodiment 7
Get carrier 100 grams of T2, in saturated leaching mode with containing 6.42g ammonium molybdate (containing MoO
382%) and the solution 80 milliliters dipping of 4.35g nickel nitrate (containing NiO51%), 120 DEG C of dryings 4 hours after dipping, 420 DEG C of roastings 3 hours guard catalyst TC-2 of the present invention.Wherein, the content of hydrogenation active metals component lists in table 2.
Embodiment 8
Get carrier 20 grams of T3, in saturated leaching mode with containing 1.2g ammonium molybdate (containing MoO
382%) and the solution 15 milliliters dipping of 2.0g nickel nitrate (containing NiO25%), 120 DEG C of dryings 4 hours after dipping, 420 DEG C of roastings 3 hours guard catalyst TC-3 of the present invention.Wherein, the content of hydrogenation active metals component lists in table 2.
Embodiment 9
Get carrier 20 grams of T4, in saturated leaching mode with containing 0.86g ammonium molybdate (containing MoO
382%) and the solution 16 milliliters dipping of 1.25g nickel nitrate (containing NiO25%), 120 DEG C of dryings 4 hours after dipping, 420 DEG C of roastings 3 hours guard catalyst TC-4 of the present invention.Wherein, the content of hydrogenation active metals component lists in table 2.
Embodiment 10
Get carrier 20 grams of T5, in saturated leaching mode with containing 1.45g ammonium molybdate (containing MoO
382%) and the solution 13 milliliters dipping of 1.30g nickel nitrate (containing NiO25%), 120 DEG C of dryings 4 hours after dipping, 420 DEG C of roastings 3 hours guard catalyst TC-5 of the present invention.Wherein, the content of hydrogenation active metals component lists in table 2.
Comparative example 5
Get carrier 20 grams of D4, in saturated leaching mode with containing 1.2g ammonium molybdate (containing MoO
382%) and the solution 12 milliliters dipping of 2.0g nickel nitrate (containing NiO25%), 120 DEG C of dryings 4 hours after dipping, 420 DEG C of roastings 3 hours guard catalyst DC-1 of the present invention.Wherein, the content of hydrogenation active metals component lists in table 2.
Comparative example 6
Get carrier 20 grams of D1, in saturated leaching mode with containing 0.86g ammonium molybdate (containing MoO
382%) and the solution 11 milliliters dipping of 1.25g nickel nitrate (containing NiO25%), 120 DEG C of dryings 4 hours after dipping, 420 DEG C of roastings 3 hours guard catalyst DC-2 of the present invention.Wherein, the content of hydrogenation active metals component lists in table 2.
Table 2
Embodiment 11-12 illustrates the hydrogenation protecting agent performance that the invention provides carrier and prepare.
Embodiment 11
The medium-sized evaluating apparatus of 200ml evaluates protective agent TC-1, and raw materials used oil is for mixing slag faulty wax oil.Appreciation condition is reaction temperature 360 DEG C, hydrogen dividing potential drop 8.0MPa, volume space velocity 0.8h
-1, hydrogen to oil volume ratio 700:1.To evaluate after 2000h Fe deposition and coke content in sample analysis protective agent.The results are shown in table 3.
XRF method (XRF semi-quantitative analysis (B-U)) is adopted to measure element of Fe content in solid sample.
Infrared absorption method (RIPP106-90) is adopted to measure carbon deposit content in protective agent (Yang Cuiding etc., Petrochemical Engineering Analysis method, publishing house of the academy of sciences, the 1990,302nd page).
Embodiment 12
According to example 11 identical condition evaluating protective agent TC-2, to evaluate after 2000h Fe deposition and coke content in sample analysis protective agent.The results are shown in table 3.
Comparative example 7
According to the condition evaluating DC-1 identical with example 11.To evaluate after 2000h Fe deposition and coke content in sample analysis protective agent.The results are shown in table 3.
Comparative example 8
According to the condition evaluating DC-2 identical with example 11.To evaluate after 2000h Fe deposition and coke content in sample analysis protective agent.The results are shown in table 3.
Table 3
| Example number | Catalyst is numbered | Fe deposits total amount, w% | Carbon content, w% |
| Embodiment 11 | TC-1 | 1.85 | 11.0 |
| Embodiment 12 | TC-2 | 1.98 | 10.3 |
| Comparative example 7 | DC-1 | 0.37 | 17.87 |
| Comparative example 8 | DC-2 | 0.2 | 18.8 |
Above evaluation result shows, compared with the hydrogenation protecting agent provided with prior art, the protective agent prepared by carrier provided by the invention holds metal ability and anti-carbon deposition ability significantly improves.
Claims (12)
1. an aluminium oxide article shaped, characterize with mercury injection method, the pore volume of described article shaped is 0.3-0.8 ml/g, and specific area is 70-220 rice
2/ gram, wherein, diameter is the 8-25% that the pore volume in 6-10nm hole accounts for total pore volume, and diameter is the 40-75% that the pore volume in 85-160nm hole accounts for total pore volume.
2. the aluminium oxide article shaped according to 1, is characterized in that, the pore volume of described article shaped is 0.4-0.7 ml/g, and specific area is 80-210 rice
2/ gram, wherein, diameter is the 10-20% that the pore volume in 6-10nm hole accounts for total pore volume, and diameter is the 45-70% that the pore volume in 85-160nm hole accounts for total pore volume.
3. the aluminium oxide article shaped according to 1, it is characterized in that, containing one or more adjuvant components be selected from IA and IIA in described aluminium oxide article shaped, with oxide basis and with described article shaped total amount for benchmark, the content of described adjuvant component is less than 10 % by weight.
4. the aluminium oxide article shaped according to 3, it is characterized in that, described IA is selected from one or more in lithium, sodium and potassium, and described IIA is selected from one or more in magnesium, calcium and barium, with oxide basis and with described article shaped total amount for benchmark, the content of described adjuvant component is 2.5-5.5 % by weight.
5. the preparation method of the aluminium oxide article shaped according to 1, comprise a kind of hydrated alumina is mixed with a kind of Alpha-alumina, shaping, dry and roasting, sintering temperature is 750-1000 DEG C, roasting time is 1-10 hour, wherein, in the mixing ratio of the hydrated alumina of butt and Alpha-alumina for 15-70:30-85, the pore volume of described hydrated alumina is 0.3-1.1 ml/g, and specific surface is 150-350 rice
2/ gram, most probable bore dia 5-20nm.
6. the method according to 5, it is characterized in that, described sintering temperature is 800-950 DEG C, roasting time is 2-8 hour, wherein, in the mixing ratio of the hydrated alumina of butt and Alpha-alumina for 30-70:30-70, the pore volume of described hydrated alumina is 0.35-1 ml/g, and specific surface is 150-300 rice
2/ gram, most probable bore dia 6-15nm.
7. the method according to 5 or 6, is characterized in that, described hydrated alumina is selected from boehmite.
8. the method according to 5, is characterized in that, comprise the step introducing one or more adjuvant components be selected from IA and IIA, with oxide basis and with described article shaped total amount for benchmark, the introduction volume of described adjuvant component is less than 10 % by weight.
9. the method according to 8, it is characterized in that, described IA is selected from one or more in lithium, sodium and potassium, and described IIA is selected from one or more in magnesium, calcium and barium, with oxide basis and with the described article shaped total amount introduction volume that is adjuvant component described in benchmark for 2.5-5.5 % by weight.
10. a hydrogenation catalyst, containing aluminium oxide shaping carrier, is characterized in that, described carrier is the article shaped in claim 1-4 described in any one.
11. hydrogenation catalysts according to 10, it is characterized in that, hydrogenation active metals component in described catalyst is selected from the metal component of at least one the VIIIth race and at least one group VIB, with oxide basis and with described catalyst for benchmark, the content of described metal component of group VIII is for being greater than 0 to being less than or equal to 8 % by weight, and the content of described metal component of group VIB is for being greater than 0 to being less than or equal to 10 % by weight.
12. catalyst according to 11, it is characterized in that, described metal component of group VIII is selected from nickel and/or cobalt, described metal component of group VIB is selected from molybdenum and/or tungsten, with oxide basis and with described catalyst for benchmark, the content of described metal component of group VIII is 0.2 ~ 4 % by weight, and the content of described metal component of group VIB is 0.5 ~ 8 % by weight.
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| CN107758708A (en) * | 2016-08-17 | 2018-03-06 | 中国石油化工股份有限公司 | A kind of aluminum oxide shaping carrier and its preparation method and application |
| CN108348896A (en) * | 2015-10-27 | 2018-07-31 | 格雷斯公司 | acid-resistant catalyst carrier and catalyst |
| CN113562749A (en) * | 2020-04-28 | 2021-10-29 | 中国石油化工股份有限公司 | Phosphorus-containing alumina with bimodal pore structure and preparation method and application thereof |
| CN113578337A (en) * | 2021-08-26 | 2021-11-02 | 青岛中瑞泰丰新材料有限公司 | Residual oil hydrogenation catalyst, and preparation method and application thereof |
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| JP2004344725A (en) * | 2003-05-20 | 2004-12-09 | National Institute Of Advanced Industrial & Technology | Impregnating solution for hydrogenation catalyst, and hydrogenation catalyst using the same |
| CN102649067A (en) * | 2011-02-24 | 2012-08-29 | 中国石油化工股份有限公司 | Hydrogenation active protective agent with aluminum oxide as carrier and preparation as well as application thereof |
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| CN1488441A (en) * | 2002-10-10 | 2004-04-14 | 中国石油化工股份有限公司 | Method for preparing alumina supporter |
| JP2004344725A (en) * | 2003-05-20 | 2004-12-09 | National Institute Of Advanced Industrial & Technology | Impregnating solution for hydrogenation catalyst, and hydrogenation catalyst using the same |
| CN102649067A (en) * | 2011-02-24 | 2012-08-29 | 中国石油化工股份有限公司 | Hydrogenation active protective agent with aluminum oxide as carrier and preparation as well as application thereof |
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| Publication number | Priority date | Publication date | Assignee | Title |
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| CN108348896A (en) * | 2015-10-27 | 2018-07-31 | 格雷斯公司 | acid-resistant catalyst carrier and catalyst |
| US11084021B2 (en) | 2015-10-27 | 2021-08-10 | W.R. Grace & Co.—Conn | Acid-resistant catalyst supports and catalysts |
| US11691124B2 (en) | 2015-10-27 | 2023-07-04 | W.R. Grace & Co.-Conn | Acid-resistant catalyst supports and catalysts |
| CN107758708A (en) * | 2016-08-17 | 2018-03-06 | 中国石油化工股份有限公司 | A kind of aluminum oxide shaping carrier and its preparation method and application |
| CN113562749A (en) * | 2020-04-28 | 2021-10-29 | 中国石油化工股份有限公司 | Phosphorus-containing alumina with bimodal pore structure and preparation method and application thereof |
| CN113562749B (en) * | 2020-04-28 | 2023-05-05 | 中国石油化工股份有限公司 | Phosphorus-containing alumina with bimodal pore structure, and preparation method and application thereof |
| CN113578337A (en) * | 2021-08-26 | 2021-11-02 | 青岛中瑞泰丰新材料有限公司 | Residual oil hydrogenation catalyst, and preparation method and application thereof |
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