CN1028019C - Isoparaffin-olefin alkylation process - Google Patents

Abstract

The present invention relates to an alkylating reaction between isoparaffin and alkene to produce alkylide. The reaction is conducted in the existence of zeolite as catalyst.

Description

Isoparaffin-olefin alkylation process

The present invention relates to make the method for alkene and isoparaffin alkylation.

Owing to use tetraethyl lead to simplify as the improvement octane additive of gasoline, the not only unleaded gasoline of result increased and also all rank gasoline in octane value increase has also been arranged.Isoparaefin-olefin alkylation is to produce the key method that mixes the highly branched alkane octane toughener in the gasoline.

Alkylation comprises alkyl group is added in the organic molecule.Therefore, isoparaffin can generate the isoparaffin of higher molecular weight with olefine reaction.Industrial alkylation often comprises C ₂-C ₅Alkene and Trimethylmethane react in the presence of acid catalyst.In the past, alkylation is included in and uses hydrofluoric acid or sulfuric acid as catalyzer under the in check temperature condition.In the sulfuric acid method, adopt low temperature to make undesired olefinic polymerization side reaction minimum, also constantly remove spent acid by the fresh acid of continuous adding and make strength of acid maintain 88-94%.The hydrofluoric acid method is more insensitive to temperature, and acid is very easy to be recovered and purifying.But hydrofluoric acid and sulfuric acid alkylation method have distinctive shortcoming, comprise and environmental correclation, consumption acid and processing corrosive deposit.Increase along with the increase of octane demand and to environmental concern, preferably develop a kind of alkylation based on the solid catalyst system.

Crystal metal silicate or zeolite are studied the catalytic process that is used for isoparaffin alkylation widely.For example, United States Patent (USP) the 3rd, 251 has been set forth the fixed bed that uses ion-exchange crystalline aluminium salt silicic acid for No. 902, and this crystalline aluminium salt silicic acid is for C ₄-C ₂₀Branched paraffin and C ₂-C ₁₂Alkene reduces the number of effective acid sites during alkylated reaction in liquid phase.This invention further is disclosed in alkene added and should allows C before the alkylation reactor ₄-C ₂₀Branched paraffin makes crystalline aluminosilicate saturated basically.

United States Patent (USP) the 3rd, 549 has disclosed for No. 557 and to be used in crystalline aluminosilicate zeolitic catalyzer specific in fixed bed, moving-bed or the fluidised bed system and to make Trimethylmethane and C ₂-C ₃Alkene carries out alkylated reaction, is preferably at the difference place of reactor alkene to be injected.

United States Patent (USP) the 3rd, 644 has disclosed for No. 565 and made paraffinic hydrocarbons and olefin alkylation in the presence of catalyzer, and this catalyzer comprises have VIII family precious metal on crystalline aluminosilicate zeolitic, carries out pre-treatment in order to promote this catalyzer of selectivity with hydrogen.

United States Patent (USP) the 3rd, 655 has disclosed employing crystalline aluminosilicate zeolitic catalyzer and has made C for No. 813 ₄-C ₅Isoparaffin and C ₃-C ₇The method of olefin alkylation is wherein used halide dose in alkylation reactor.Isoparaffin and alkene add alkylation reactor with certain concentration, and catalyzer is constantly regeneration outside alkylation reactor.

United States Patent (USP) the 3rd, 893 has disclosed for No. 942 to adopt and has contained the isoparaffin alkylation method that VIII family metal zeolite is a catalyzer, when this catalyst member inactivation, needs periodically in gas phase with hydrogen hydrogenation to activate this catalyzer.

United States Patent (USP) the 3rd, 236 has disclosed the crystalline aluminosilicate zeolitic that uses the mol ratio about 3 of silicon and aluminium in alkylated reaction for No. 671, and this patent has also disclosed the metal that uses all exchanges and/or has been immersed in this class zeolite.

United States Patent (USP) the 3rd, 624 has disclosed for No. 173 and used the zeolite catalyst that contains gadolinium in isoparaffins alkylation.

United States Patent (USP) the 3rd, 738 has disclosed the paraffinic hydrocarbons and the ethylene alkylation that adopt the zeolite catalyst that VIII family metal component is arranged for No. 977, and the existing hydrogen of catalyzer carries out pre-treatment.

United States Patent (USP) the 3rd, 865 has disclosed for No. 894 with anhydrous basically acid zeolite, for example acid zeolite Y(zeolite HY) and the halogenide auxiliary material make C ₄-C ₆Isoparaffin and C ₃-C ₉The monoolefine alkylation.

United States Patent (USP) the 3rd, 917 has disclosed the method that makes isoparaffin and olefin alkylation with solid particle catalyst that can adsorbs olefins for No. 738.Isoparaffin and olefin are formed reactant flow, inlet end place at adsorption zone contacts with granules of catalyst, reactant and catalyzer following current are passed through then, so that before making reactant and catalyst mixture introduce alkylation zone, the alkene of manipulated variable can be adsorbed on the catalyzer.The absorption of this manipulated variable alkene it is said the polymerization that can prevent alkene during the alkylation.

United States Patent (USP) the 4th, 377 has disclosed employing ZSM-20 No. 721, is the Isoparaffin-olefin alkylation process of the catalyzer of HZSM-20 or rare-earth cation exchange ZSM-20 preferably.

United States Patent (USP) the 4th, 384, disclose isoparaffin and olefin alkylation for No. 161 and produced the method for alkylide, it adopts can adsorb 2,2, the large pore zeolite of 4-trimethylpentane, for example ZSM-4, ZSM-20, ZSM-3, ZSM-18, zeolite Beta, faujusite, mordenite, zeolite Y and contain the rare earth metal form, and such as Louis's acid as catalyst of boron trifluoride, antimony pentafluoride or aluminum chloride.Thereby use large pore zeolite can carry out effective alkylated reaction with high alkene space velocity and low isoparaffin/alkene ratio in conjunction with activity and selectivity that Louis acid can greatly increase zeolite according to the report of this patent.

The invention provides the alkylating method of isoparaffin and alkene, it is included under the catalyzer existence and makes isoparaffin and olefine reaction, and this catalyzer is a synthetic porous crystalline zeolite, has the X ray diffracting spectrum that comprises that numerical value is as shown in table 1 basically.

An alkylation catalyst optionally measurement index is G ⁺ ₉Yield.This component is normal because the alkene generation oligomerisation reaction result alkylation yield of charging descends, and has reduced the quality of alkylide and may form acid pulpous state component.Use zeolite alkylated catalyst to reduce G in the methods of the invention ⁺ ₉Yield, the known zeolite alkylated catalyst of this class are the HY that for example discloses in No. the 3rd, 865,894, above-mentioned United States Patent (USP).

The alkylide of producing with the inventive method is high-quality on research octane number (RON) and motor-method octane number basis, and it is particularly suitable for blending and goes in the gasoline pool.

The synthetic porous crystalline zeolite that is used for alkylation of the present invention has the X-ray diffraction diagram spectrum that comprises as the listed spectral line of following table I under its calcined form:

The table I

D-interplanar distance (A) relative intensity, I/I ₀* 100

12.36±0.4 W-VS

11.03±0.2 M-S

8.83±0.14 M-VS

6.18±0.12 M-VS

6.00±0.10 W-M

4.06±0.07 W-S

3.91±0.07 M-VS

3.42±0.06 VS

The following table II is listed spectral line more specifically

The table II

D-interplanar distance (A) relative intensity, I/I ₀* 100

30.0±2.2 W-M

22.1±1.3 W

12.36±0.4 M-VS

11.03±0.2 M-S

8.83±0.14 M-VS

6.18±0.12 M-VS

6.00±0.10 W-M

4.06±0.07 W-S

3.91±0.07 M-VS

3.42±0.06 VS

The following table III is also listed spectral line more specifically

The table III

D-interplanar distance (A) relative intensity, I/Io * 100

12.36±0.4 M-VS

11.03±0.2 M-S

8.83±0.14 M-VS

6.86±0.14 W-M

6.18±0.12 M-VS

6.00±0.10 W-M

5.54±0.10 W-M

4.92±0.09 W

4.64±0.08 W

4.41±0.08 W-M

4.25±0.08 W

4.10±0.07 W-S

4.06±0.07 W-S

3.91±0.07 M-VS

3.75±0.06 W-M

3.56±0.06 W-M

3.42±0.06 VS

3.30±0.05 W-M

3.20±0.05 W-M

3.14±0.05 W-M

3.07±0.05 W

2.99±0.05 W

2.82±0.05 W

2.78±0.05 W

2.68±0.05 W

2.59±0.05 W

More particularly, listed the incinerating crystalline material of the x-ray diffraction pattern that comprises spectral line in the following table IV.

The table IV

D-interplanar distance (A) relative intensity, I/I ₀* 100

30.0±2.2 W-M

22.1±1.3 W

12.36±0.4 M-VS

11.03±0.2 M-S

8.83±0.14 M-VS

6.86±0.14 W-M

6.18±0.12 W-VS

6.00±0.10 W-M

5.54±0.10 W-M

4.92±0.09 W

4.64±0.08 W

4.41±0.08 W-M

4.25±0.08 W

4.10±0.07 W-S

4.06±0.07 W-S

3.91±0.07 M-VS

3.75±0.06 W-M

3.56±0.06 W-M

3.42±0.06 VS

3.30±0.05 W-M

3.20±0.05 W-M

3.14±0.05 W-M

3.07±0.05 W

2.99±0.05 W

2.82±0.05 W

2.78±0.05 W

2.68±0.05 W

2.59±0.05 W

These value measured by standard techniques.Radioactive rays are K-α two-wires of copper and adopt the diffractometer that scintillometer is housed and is associated with computer.Measure peak height, 1 and as the position of 20 function with the algorithm on the computer that links with diffractometer, wherein 0 is the Bragg angle.Therefrom can measure relative intensity 100I/I ₀, I wherein ₀Be corresponding to the strongest spectral line of registration line or the intensity at peak, and the d interplanar distance, it is unit (A) with the dust.A little less than the relative intensity symbolically W-, M-is medium in table I-IV, and S-is strong, and VS-is extremely strong.About intensity, Chang Zuowei is as giving a definition:

W＝0-20

M＝20-40

S＝40-60

VS＝60-100

Be understood that these X-ray diffracting spectrums are features of all kinds zeolite.Sodium type and other are cationic to be to have the identical collection of illustrative plates that the interplanar distance trace moves and relative intensity changes basically.Than X, for example some other trickle variations may take place in the mol ratio of silicon and aluminium and heat treated degree thereof according to Y.

Be used for zeolite of the present invention the composition that comprises following molar relationship formula typically arranged:

X ₂O ₃∶（n）YO ₂

Wherein X is a trivalent element, and for example aluminium, boron, iron and/or gallium are aluminium preferably, and Y is the quadrivalent element such as silicon and/or germanium, is silicon preferably, and n is at least 10, often from 10-150, is 10-60, preferably 20-40 preferably.In the synthetic form, on anhydrous basis and at every several moles of YO ₂Terms of oxide moles aspect zeolite have the following formula structure:

（0.005-0.1）Na ₂O∶（1-4）R∶X ₂O ₃∶nYO ₂

Wherein R is an organic constituent.Because Na and R component exist when crystallization, and be relevant with zeolite, but they can remove easily by the post crystallization method, will do specific elaboration below.

Zeolite used herein is a thermostability, it have big surface-area (by BET[Bruenaner, Emmet and Teller] test record greater than 400m ²/ gs).In addition, the equilibrium adsorption value of zeolite is generally greater than 4.5%(weight), for cyclohexane vapor usually greater than 7%(weight), for the normal hexane steam greater than 10%(weight), for water vapour more preferably greater than 10%(weight), for water vapour more preferably greater than 10%(weight).Shown in following formula, therefore the synthetic zeolite does not almost have the Na positively charged ion like this, thereby has the acidic catalyst activity.Therefore it can needn't at first carry out switch process as alkylation catalyst here.But, extend and come, can be substituted by ion-exchange with other positively charged ion according to original sodium cation of the such synthetic materials of existing known technology, be that part is substituted at least.Replace preferably and stop before positively charged ion comprises metal ion, hydrogen ion, hydrogen, for example, stop before ammonium ion, hydrogen ion, the hydrogen,, for example, ammonium ion and composition thereof.Best positively charged ion is those materials that can produce catalytic activity in alkylation among this.They comprise the metal of II A family, III A family, IV A family, I B family, II B family, III B family, IV B family and VIII family in hydrogen, rare earth metal and the periodic table of elements.

Before alkylation catalyst used, zeolite should be heat-treated the part or all of organic component that wherein exists to remove.

Zeolite alkylated catalyst used herein also can with the hydrogenation component use of combining closely, hydrogenation component is such as tungsten, vanadium, molybdenum, rhenium, nickel cobalt, chromium, manganese or such as the precious metal of platinum or palladium, they can carry out the hydrogenation-dehydrogenation effect.This class component can be with zeolite and/or is arbitrarily constituted the matrix Chemical bond and/or the physical bond of zeolite.Like this, for example, hydrogenation component can be introduced catalyst composition by cocrystallization, convert composition to III A family element in structure, for example aluminium floods its wherein or the close physical mixing.This class component can be immersed in the zeolite or on the zeolite, for example, with regard to platinum, handle zeolite with containing the platinum solion.Like this, the suitable platinic compound that is used for this purpose comprises platinichloride, platinous chloride and contains all cpds of platinum amine coordination compound.

Be used as alkylation catalyst in this inventive method before, this zeolite is answered partial dehydration at least.These can be under 200 ℃-595 ℃ in such as air, nitrogen atmosphere etc., and under atmospheric pressure, is lower than to make crystallization heating 30 minutes to 48 hours under normal atmosphere or the super-atmospheric pressure.Dehydration also can at room temperature be carried out, and it just is placed on crystalline material in the vacuum for a long time just can reach suitable degree of dehydration.

Being used for zeolite of the present invention also can make from reaction mixture, reaction mixture contains basic metal or alkaline-earth metal (M), for example, sodium or potassium, their positively charged ion, the oxide compound of the trivalent element X of aluminium for example, the oxide compound of the quadrivalent element of silicon (Y) for example, organic (R) directing agent, hexamethylene imine and water are with regard to oxide molar is quantitative.The component of described reaction mixture is in following scope:

Useful preferred of reaction reagent

YO ₂/X ₂O ₃10-60 10-40

H ₂O/YO ₂5-100 10-50

OH ^-/YO ₂0.01-1.0 0.1-0.5

M/YO ₂0.01-2.0 0.1-1.0

R/YO ₂0.05-1.0 0.1-0.5

In preferred synthetic method, YO ₂Reaction reagent contains the solid YO of fundamental quantity ₂, for example contain 30%(weight at least) and solid YO ₂, YO wherein ₂Be silicon-dioxide, use contains 30%(weight at least) silica material of solid silica, for example, Ultrasil(throw out, contain 90%(weight) the spray-dired silicon-dioxide of silicon-dioxide) or Hisil(contain 87%(weight) silicon-dioxide, 6%(weight), free H ₂O and 4.5%(weight) hydration in conjunction with H ₂The sedimentary hydration SiO of O ₂, its granular size is 0.02 micron) and be crystalline structure preferably in the said mixture.If adopt another kind of silica material, for example, Q-Brand(comprises 28.8%(weight) SiO ₂, 8.9%(weight) Na ₂O and 62.3%(weight) water glass of water), crystallization almost can not get required zeolite and the impure phase of other crystalline structure, for example can produce ZSM-12.Therefore, YO preferably ₂, for example silicon-dioxide is with containing 30%(weight at least) and solid YO ₂SiO for example ₂Raw material is preferably used 40%(weight at least) solid YO ₂, silicon-dioxide for example.

Under static or the agitation condition such as polypropylene vial be lined with tetrafluoroethylene or the suitable reaction vessels of stainless autoclave in make required zeolite carry out crystallization.Crystallization is everlasting and was carried out 25 hours to 60 days under 80-225 ℃.After this, crystal is separated from liquid and is reclaimed.

Calculate according to producing the crystal gross weight, better 0.1% at least 0.01%, be preferably 1% crystal seed and exist and promote crystallization down.

Before using method of the present invention, this zeolite is that tackiness agent combines with other material preferably, and it can tolerate temperature and other condition that adopts in the isoparaffin alkylation method of the present invention.The suitable binder material comprises the zeolite of active and non-active material and synthetic or natural generation and such as potter's clay, silicon-dioxide and/or such as the inorganic materials of the metal oxide of aluminum oxide.The latter be natural formation or gelatinous throw out or comprise silicon-dioxide and the mixture of metal oxide.Use and zeolite bonded adhesive material, promptly tackiness agent is just in conjunction with transformation efficiency and/or the selectivity of entering to change catalyzer when synthetic, and tackiness agent itself has catalytic activity.Can be suitably inversion quantity can be controlled so that can obtain the product of isoparaffin alkylation economically and control the formation of product and needn't control speed of reaction with other means as the non-active material of thinner.These materials can be bonded to natural potter's clay, for example in wilkinite and the kaolin to improve the shatter strength of zeolite under business-like isoparaffin alkylation operational condition.Since good shatter strength can prevent or delayed catalyst becomes flour, it has just made good contribution for commercial applications.

Can comprise polynite and kaolin group with the potter's clay of the natural formation of this combination of zeolites, this family comprises inferior wilkinite, be called the kaolin of Dixie, Mc Namee, Georgia and Florida potter's clay or main inorganic components and be halloysite, kaolin, open soil (diokite), nakrite (nacrite) and wriggle and fall into other material of soil etc.This class potter's clay can use by original unprocessed state, or at first is used through roasting, acid treatment or chemical modification.Also comprise inorganic oxide, famous aluminum oxide with the useful tackiness agent of combination of zeolites.

Except aforesaid adhesive material, this zeolite also can with combine substantially such as silicon-dioxide one Thorotrast, silica-beryllia, silica-titania and such as the inorganic oxide of silica-alumina-Thorotrast, silica-alumina-zirconium white, silica-alumina-magnesium oxide and silica-magnesia-zirconic ternary composition.To be colloidal forms be favourable so that the extruding of adherent catalyst component to small part aforementioned substrates material.

The relevant nature of zeolite and inorganic oxide matrix can be different and different greatly with zeolite content, and its content range is a 1-9.5%(weight), be that when the composition of preparation was the pearl form, the zeolite content scope was a 2-80%(weight) more commonly.

By steam the stability of alkylation catalyst of the present invention is increased, the at least 300 ℃ of temperature of steam (for example 300-650 ℃) that make zeolite and for example 5-100% are at 101-2, and 500Kpa pressure contact at least one hour (for example 1-200 hour) down can carry out this process easily.In example more specifically, catalyzer can under atmospheric pressure steam under 315-500 ℃ 2-25 hour and makes with 75-100% steam.

The alkylation catalyst that uses in the inventive method can comprise lewis promoters except above-mentioned zeolite.Lewis acid is generally considered to be a molecule, and it can combine by forming covalent chemical bond with another molecule or ion, and this chemical bond has two from second kind of molecule or ionic electronics, and in other words, Lewis acid is a kind of electron acceptor.Lewis acidic example comprises boron trifluoride (BF ₃), antimony pentafluoride (SbF ₅) and aluminum chloride (AlCl ₃).The present invention expects that other Lewis acid that uses is included in " Friedel-Crafts and correlated response reagent " Interscien Publishers, the Lewis acid that discloses in III and the IV chapter (1963).The better Lewis acid that uses in alkylation of the present invention is BF ₃With regard to BF ₃, this promotor is present in preferably in the alkylation zone that its consumption requires can the saturated zeolite catalyst component, and this not only will consider zeolite itself but also will consider other material, for example, can mix the tackiness agent or the body material of zeolite.

Here the service temperature of alkylation is in very wide scope, for example-40-400 ℃, when existing, lewis promoters can use lower temperature.The temperature of the lewis promoters of Shi Yonging is usually at-40-250 ℃ like this, preferably between-20-100.When not adopting lewis promoters, temperature from-25-400 ℃, is 75-200 ℃ usually preferably.Actual upper limit service temperature often fixes on the temperature of avoiding producing unwanted side reaction.

Can in very wide scope, change with in the method pressure, for example, from being lower than normal atmosphere to 34580Kpa(5000Psig), preferably from the 100-7000Kpa(1 normal atmosphere to 1000Psig).

The amount of zeolite of using in this alkylation is different and different with corresponding a large amount of restrictions.In general, the amount of zeolite of measurement alkene weight hourly space velocity can be in the 0.01-100 scope, preferably in the scope of 0.1-20.

The isoparaffin reaction reagent that is used in this alkylation often has up to 20 carbon atoms, and 4-8 carbon atom arranged preferably, for example Trimethylmethane, 3-methyl hexane, 2-methylbutane, 2,3-dimethylbutane and 2,4-dimethylhexane.

Olefine reaction agent used herein often contains the 2-12 carbon atom.Representational example is ethene, propylene, butene-1, butene-2, iso-butylene-amylene, hexene, heptene and octene.C most preferably ₃And C ₄Alkene and their mixture.

In general, in the charging of blended hydrocarbon, the ratio of total isoparaffin and total olefin alkylation base can be 0.5: 1-500: 1, and preferably from 3: 1-50: 1.Isoparaffin and/or olefine reaction reagent can be gas phase or liquid phase, purified, can perhaps reaction reagent be contacted with catalyst composition from dissociating out the blended mixture intentionally during promptly with other material dilution by carrier gas or thinner such as nitrogen.

Reaction reagent can be operated one or more other materials and introduces alkane it changes reaction zone with strengthening total conversion rate.Therefore, for example, in reaction zone, can exist quite a spot of hydrogen and or hydrogen acceptor to suppress catalyst aging.Water and/or alkylation conditions can provide down the material of water such as alcohol for this purpose, also can be introduced in the reaction zone.The material that oxygen and/or tend to suppresses olefin oligomerizationization also can exist.

In the time of in water is introduced alkylation reactor, based on total hydrocarbon feed speed, it is easily with 0.1ppmw to 1%(weight), be 0.1ppmw to 500ppmw charging more preferably.Interchangeablely be, water can be introduced earlier in the zeolite catalyst, and suitable amounts is the 0.5-25% that accounts for catalyst weight, is 1-10% preferably.

Alkylation of the present invention can be by batch-type, carry out to semicontinuous or continuity, and its adopts the fixed bed or the moving-bed of zeolite catalyst component.Example is to use catalyst zone preferably, wherein the hydrocarbon charging be by zeolite catalyst the moving-bed following current by or adverse current pass through.After the use, the latter is directed to the breeding blanket, removes in the breeding blanket and has propped up coke, for example, at high temperature (for example in the air) burns or uses solvent extraction in oxygen containing atmosphere, and then, the regenerated catalyst recycle enters zone of transformation further to contact with organic reactant.

The present invention does more specific description with embodiment with reference to the accompanying drawings, wherein:

Fig. 1-5 is the X-ray diffracting spectrum that embodiment 1,3,4,5 and 7 baked crystalline materials produce in succession.

In an embodiment, to the sorptive power of water, hexanaphthene and/or normal hexane and the sorption data of setting up, following is the equilibrium adsorption value that records for relatively:

The sorbent material that fused is placed in the adsorption chamber with required purity adsorbate steam contacts, be pumped to and be less than 1mmHg, again with 1.6Kpa(12Forr) water vapour or 5.3Kpa(40Torr) normal hexane steam or 5.3Kpa(40Torr) cyclohexane vapor contacts, and pressure will be lower than 90 ℃ of vapour-liquid equilibrium pressure of each adsorbate down.By add the adsorbate steam make pressure keep constant (approximately ± 0.5mmHg) between adsorption cycle with potentiostat control, this adsorption time is no more than about 8 hours.Because adsorbate adsorbed by crystalline zeolite, pressure descends and makes the valve open of potentiostat, so just allows store the extremely pressure of above-mentioned control in more adsorbate steam inlet chambers.When the change deficiency of pressure so that potentiostat then sorption is complete when movable.Calculate the weight that increases, as the adsorptive power of roasting adsorptive g/100g sample.Here its equilibrium adsorption value of the zeolite of usefulness for water vapour always greater than 10%(weight), for cyclohexane vapor generally greater than 4.5%(weight), usually greater than 7%(weight), for the normal hexane steam greater than 10%(weight).

When detecting the α value, noticed that the α value is the approximate index of the catalytic cracking activity of the catalyzer of comparing with standard catalyst, the α value has provided speed of relative movement constant (the normal hexane conversion rates of unit time per volume of catalyst).The activity that it is based on highly active silica-alumina catalyst for cracking is got the α value and is 1(rate constant-0.016 second ^-1).Here J.Calalysis is seen in used α test, 61, pp.390-396(1980) described in.Have been noted that the relevant characteristic rate constant of many acid catalyzed reactions is proportional for specific crystalline silicate catalyst and α value, even toluene disproportionation, xylene isomerization, alkene transform and the speed of methanol conversion (is seen " The Active Side of Acidie Aluminesilicate Cala lysts " Nature 309 volumes, No. 5969, on June 14th, 589-591 number).

Embodiment 1

With 1 part of sodium aluminate (43.5%Al ₂O ₃, 32.2%Na ₂O, 25.6%H ₂O) be dissolved in and contain 1 part of 50%NaOH solution and 103.13 parts of H ₂In the solution of O.Inwardly add 4.50 parts of hexamethylene imines.8.55 parts of Ultrasil are added in the solution of gained.Ultrasil is a kind of throw out, spray-dired silicon-dioxide (about 90%SiO ₂).

Reaction mixture has the composition of following molar ratio.

SiO ₂/Al ₂O ₃-30.0

OH ^-/SiO ₂-0.18

H ₂O/SiO ₂-44.9

Na/SiO ₂-0.18

R/SiO ₂-0.35

Wherein R is a hexamethylene imine.

Make mixture crystallization 7 days in stainless steel reactor under 150 ℃ under agitation condition.The filtering for crystallizing product.Wash with water and drying under 120 ℃.538 ℃ of following roastings 20 hours, X-ray diffracting spectrum contained the main spectral line of listing just like the table V.Fig. 1 has shown the X-ray diffracting spectrum of baked product.The sorptive power of the baked material that records is:

H ₂O 15.2%(weight)

Hexanaphthene 14.6%(weight)

Normal hexane 16.7%(weight)

The zeolite surface area that records is 494m ²/ g.

The chemical composition of unfired material is measured as follows:

Component wt.%

SiO ₂66.9

Al ₂O ₃5.40

Na 0.03

N 2.27

Ash 76.3

SiO ₂/ Al ₂O ₃, molar ratio 21.1

(the table V is seen the literary composition back)

Embodiment 2

The crystallized product of a roasting of embodiment 1 carries out the α test and finds that its α value is 224.

Embodiment 3-5

With three kinds of synthesis reaction mixtures that separate of preparation of compositions of listing in the table VI.Mixture is prepared with sodium aluminate, sodium hydroxide, Ultrasil, hexamethylene imine (R) and water.Successively with mixture under autogenetic pressure, in stainless steel autoclave, be incubated 7 days respectively under 150 ℃, 143 ℃ and 150 ℃, 8 days and 6 days.By filtering unreacted component is separated from solid, washed with water then, dry down at 120 ℃ then.Allow the product crystal carry out X-ray diffraction analysis, sorption analysis, surface-area analysis and chemical analysis.List sorption, surface-area and chemico-analytic result in the table VI, listed the collection of illustrative plates of X-ray diffraction among Fig. 2,3 and 4 successively.Measure the sorption and the surface-area of product of roasting.

Embodiment 6

With baked (538 ℃ roasting 3 hours) of quantitative embodiment 3,4 and 5, crystallization estersil salt product carries out the α test, and its α value is followed successively by 227,180 and 187.

Embodiment 7

In order to confirm that required zeolite prepares in a large number, 1200 gram hexamethylene imines are added to close 268 gram sodium aluminates, 267 gram 50%(NaOH solution and 11,800 gram H ₂In the solution of O.In the solution that merges, add 2.280 gram Ultrasil silicon-dioxide.(about 200rpm makes its crystallization, and crystallization time is 59 hours stirring the mixture in 5 gal reactor under 145 ℃.Wash product and dry down with water at 120 ℃.

Fig. 5 has listed drying products crystalline X-ray diffracting spectrum, and it confirms that product is a crystalline material of the present invention.The table VII has been listed the result of product chemical composition, surface-area and adsorption analysis;

The table VII

Product composition (without roasting)

C 12.1(weight) %

N 1.98(weight) %

Na 640ppm

Al ₂O ₃5.0(weight) %

SiO ₂74.9(weight) %

SiO ₂/ Al ₂O ₃, mol ratio 25.4

Absorption, %(weight)

Hexanaphthene 9.1

Normal hexane 14.9

H ₂O 16.8

Surface-area, m ²/ g 479

Embodiment 8

With embodiment 7 gained 25 the gram solid crystallized products in the flowing nitrogen atmosphere in 538 ℃ of following roastings 5 hours, and then with 5% oxygen (all the other are N ₂) purify 16 hours down at 538 ℃.

With the baked material sample of every part 3 gram with 100 milliliters of 0.1NTEABr, TPABr and LaCl ₃Solution carries out ion-exchange dividually.Every kind of exchange was at room temperature carried out 24 hours and triplicate.By filtering the sample of collecting exchange, wash with water to non-halogen thing and dry.The composition of the sample that exchanged is made following table, and it shows the exchange capacity of this crystalline silicate to different ions.

Ion-exchange

Ionic composition %(weight) TEA TPA La

Na 0.095 0.089 0.063

N 0.30 0.38 0.03

C 2.89 3.63 -

La - - 1.04

Embodiment 9

The sample of the La that obtains from embodiment 8 one exchange is a 14-25 order size, then in air in 538 ℃ of following roastings 3 hours, be 173 through the value of the material of roasting.

Embodiment 10

Roasting sample La one exchange material that will from embodiment 9, obtain under 649 ℃ in 100% steam decatize 2 hours tempestuously.The α value of the sample that decatize is crossed is 22, and this expression zeolite has fabulous stability violent the mistake under the hydrothermal treatment consists.

Embodiment 11

This embodiment has set forth prepare zeolite, and the X in the wherein above-mentioned general formula is a boron.2.59 parts of boric acid are added to contain 1 part of 45%KOH solution and 42.96 parts of H ₂In the solution of O.Inwardly add 8.56 parts of Ultrasil silicon-dioxide, mixture is mixed.The hexamethylene imine that in mixture, adds 3.88 parts (weight).

Reaction mixture has the following composition of mol ratio.

SiO ₂/B ₂O ₃-6.1

OH ^-/SiO ₂-0.06

H ₂O/SiO ₂-19.0

K/SiO ₂-0.06

R/SiO ₂-0.30

Wherein R is a hexamethylene imine.

Under 150 ℃ of agitation conditions, make mixture crystallization 8 days in stainless steel reactor.The filtering for crystallizing product washes with water and drying under 120 ℃.Portion of product 540 ℃ of following roastings 6 hours, is found that it has following sorptive power.

H ₂O 11.7%(weight)

Hexanaphthene 7.5%(weight)

Normal hexane 11.4%(weight)

The surface-area (BET) of measuring baked crystalline material is 405m ²/ g.

Chemical composition without the roasting material is measured as follows:

N 1.94%(weight)

Na 175ppm

K 0.60%(weight)

Boron 1.04%(weight)

Al ₂O ₃920ppm

SiO ₂75.9%(weight)

Ash 74.11%(weight)

SiO ₂/ Al ₂O ₃, mol ratio 1406

SiO ₂/ (Al+B) ₂O ₃, mol ratio 25.8

Embodiment 12

Use NH ₄The baked crystalline product of the part of Cl Processing Example 11 carries out roasting again.Last crystallized product is carried out the α test, find that its α value is 1.

Embodiment 13

This embodiment sets forth the another kind of method for making of zeolite, and X is a boron in above-mentioned general formula.2.23 parts of boric acid are added to 1 part of 50%NaOH solution and 73.89 parts of H ₂In the solution of O.In this solution, add 15.29 parts of Hi Sil silicon-dioxide.Add 6.69 parts of hexamethylene imines then.Reaction mixture has the following composition of mol ratio.

SiO ₂/B ₂O ₃-12.3

OH ^-/SiO ₂-0.056

H ₂O/SiO ₂-18.6

K/SiO ₂-0.056

R/SiO ₂-0.30

Wherein R is a hexamethylene imine.

Under 300 ℃, mixture was placed the stainless steel reactor stirred crystallization 9 days.The filtering for crystallizing product washes with water and drying under 120 ℃.Measure the sorptive power of roasting material (540 ℃ of following roastings 6 hours).

H ₂O 14.4%(weight)

Hexanaphthene 4.6%(weight)

Normal hexane 14.0%(weight)

The surface-area that records the roasting crystalline material is 438m ²/ g.

Record without the chemical composition of roasting material as follows:

Component weight %

N 2.48

Na 0.06

Boron 0.83

Al ₂O ₃0.50

SiO ₂73.4

SiO ₂/ Al ₂O ₃, mol ratio 249

SiO ₂/ (Al+B) ₂O ₃, mol ratio 28.2

Embodiment 14

The roasting crystallized product of a embodiment 13 is carried out the α test, find that its α value is 5.

Embodiment 15

This embodiment will be used in zeolite catalysis performance of the present invention in the alkylated reaction of Trimethylmethane and 2-butylene and the catalytic performance of zeolite HY compares.

A. prepare zeolite of the present invention.

4.50 parts of hexamethylene imines are added to contain 1.01 parts of sodium aluminates, 1.00 parts of 50%(NaOH, 8.56 parts of Ultrasil, VN ₃With 44.29 parts of deionization H ₂Produce zeolite of the present invention in the mixture of O.Reaction mixture is heated to 143 ℃ (290 °F) and stirred crystallization in the autoclave under this temperature.After producing whole crystallizations, from autoclave, remove most of hexamethylene imines, zeolite crystal is separated from raffinate, use deionized water wash, with ammonium ion exchange and dry by filtering by the control distillation.This zeolite of a part exchanges with aqueous ammonium nitrate solution again.Then with this material dried overnight under 120 ℃ (250), at 480 ℃ (900) and 3v/v/minN ₂The 50%(volume is used in following roasting 3 hours then) air/50%(volume) N ₂With 3v/v/min) speed also handled 1 hour down at 480 ℃ (900 °F).Temperature is risen to 540 ℃ (1000 °F) with 3 ℃ (5F)/minute speed make roasting complete, convert 100% air (3v/v/min) at last to and under this temperature, kept 6 hours.Its alpha active of the zeolite of gained is 323.Surface-area is 455m ²/ g also contains 28ppm sodium.

B. the preparation of zeolite HY

With 60 gram NaY and 1NNH ₄NO ₄At room temperature exchange 1 hour and make the HY catalyzer.Filtering catalyst, washing, and repeated exchanged process.The Y zeolite roasting that under 540 ℃ (1000), in air, ammonium salt is exchanged 3 hours.The alpha active of final material is 61, and surface-area is 721m ²/ g, and contain 3.0%(weight) sodium.

C. the alkylating of Trimethylmethane and 2-butylene

In order to assess the boiling characteristic of above-mentioned zeolite, in autoclave, separately carry out alkylated reaction in a large number in batches.Initial step comprises that belonging to 10 gram catalyzer adds in the reactor, seals container then.Then about 350 gram Trimethylmethane/2-butylene are imported autoclave and stir slurry like material at successive nitrogen pressure duration of test.In order to begin reaction, allow nitrogen pressure be lower than 1135Kpa(150psig), and heat to system with 3 ℃ of (5)/minute speed.End reaction condition in each reaction is 120 ℃ (250 °F), and autogenetic pressure is 3410Kpa or (480psig), stirring velocity is 500rpm.

The following table VIII has been listed the result of alkylated reaction.(the table VIII is seen the literary composition back)

Shown in these data, under identical conversion condition, compare with using zeolite HY catalyzer, use alkylation catalyst of the present invention in fact to obtain more trimethyl propane alkylide, less than G ⁺ ₉Product is less significantly.

Embodiment 16

This embodiment is with BF of the present invention ₃The alkylation performance and the BF of-promoted zeolite alkylated catalyst composition ₃-promoted silicon-dioxide alkylation catalyst composition is compared.4.49 parts of (weight) hexamethylene imines are added to contain 1.00 parts of sodium aluminates, 1.00 parts of 50%NaOH, 8.54 parts of Utrasil VN ₃With prepare catalyzer of the present invention in the mixture of 44.19 parts of deionized waters.Reaction mixture is heated to 143 ℃ (290 °F) and under this temperature in autoclave stirred crystallization, after reaching whole crystallizations, from autoclave, remove most of hexamethylene imines by the control distillation, from raffinate, isolate crystallization of zeolites, with deionized water wash and dry by filtering.At 1000 N ₂In roasting 6 hours, then with the aqueous ammonium nitrate solution exchange and in 1000 air roasting made activating zeolite in 6 hours.

In the reaction that separates, every kind of aforementioned catalyst composition of 10 grams and 300 milliliters of Trimethylmethanes are added in the reactor, then reactor content being cooled to required alkylation temperature, constantly stirring simultaneously, with 3%(weight with 1900rpm speed) flow velocity of (accounting for total hydrocarbon charging) is BF ₃Gas is introduced in the reactor.Then the alkene of charging is constantly introduced in the reactor to cause alkylated reaction.Trimethylmethane and total olefin molar ratio are 10: 1, and temperature of reaction is as follows to be 0 or 20 ℃, and weight space-time speed (WHSV) (on the basis of total olefin) is 1.3.List the composition of charging in the table IX, listed the result of two kinds of catalyst composition alkylated reactions in the table X:

The table IX

The composition of paraffinic hydrocarbons-alkene charging

Alkene propylene+butylene

Trimethylmethane: olefin molar ratio 12: 1

Feed components weight %

Propylene 3.30

Iso-butylene 1.24

1-butylene 1.01

2-butylene 2.14

Iso-butylene 92.31

(the table X is seen the literary composition back)

Embodiment 17

Basic repetition embodiment 16, but its feed composition is shown in the following table XI

The table XI

The composition of paraffinic hydrocarbons-alkene charging

Alkene propylene+butylene

Trimethylmethane: olefin molar ratio 5.7: 1

Feed components weight %

Propylene 5.60

Iso-butylene 2.90

1-butylene 2.00

2-butylene 4.45

Iso-butylene 84.40

N-butene 0.65

The result of alkylated reaction is shown in the following table VII:

(the table VII is seen the literary composition back)

Embodiment 18

Basic repeat embodiment 16 but its feed composition shown in following table X III:

Table X III

Paraffinic hydrocarbons-the compositions of olefines of charging

Alkene propylene+butylene

Trimethylmethane: olefin molar ratio 10: 1

Feed components weight %

Iso-butylene 5.73

1-butylene 0.26

2-butylene 2.98

Iso-butylene 90.93

N-butene 0.10

The result of alkylated reaction is shown in following table X IV:

Embodiment 19

Basic repetition embodiment 16, but its feed composition is shown in following table X V:

Table X V

Paraffinic hydrocarbons-alkene feed composition

Alkene propylene+butylene

Trimethylmethane: olefin molar ratio 12.9: 1

Feed components weight %

Propylene 3.22

Iso-butylene 2.74

1-butylene 0.15

2-butylene 1.24

Iso-butylene 92.50

N-butene 0.15

The result of alkylated reaction is shown in following table X VI:

(table X VI is seen the literary composition back)

Embodiment 20

Basic repetition embodiment 16, but its feed composition is shown in following table X VII:

Table X VII

Paraffinic hydrocarbons-alkene feed composition

The alkene butylene

Trimethylmethane: olefin molar ratio 9.6: 1

Feed components weight %

2-butylene 9.4

Iso-butylene 90.60

The result of alkylated reaction is shown in following table X VIII:

(table X VIII is seen the literary composition back)

Embodiment 21-24

Use BF of the present invention ₃-promoted zeolite alkylated catalyst comes the process (embodiment 21) of repetition embodiment 16, with the result with compare with the similar catalyzer gained result who is added with water.(embodiment 22 and 23), and and BF ₃/ H ₂The O catalyst system relatively.The result comprehensively lists in the table X IX.

(table X IX is seen the literary composition back)

From table X IX as seen, in above method condition, BF ₃/ zeolite/H ₂The O system is than the big (100vs of anhydrous catalyst activity.The 57%(conversion of olefines) and produce alkylate (6.2vs.71.7%(weight) C of more amount ¹ ₉).In addition, BF ₃/ zeolite/H ₂The alkylide that the O catalyzer produces compares BF ₃/ H ₃The product that the O system produces is outstanding, and (product is greater than C ₈Be lower than G ⁺ ₉).

The table V

20-angle d-interplanar distance (A) I/I ₀

2.80 31.55 25

4.02 21.98 10

7.10 12.45 96

7.95 11.12 47

10.00 8.85 51

12.90 6.86 11

14.43 6.18 42

14.72 6.02 15

15.90 5.57 20

17，81 4.98 5

20.20 4.40 20

20.91 4.25 5

21.59 4.12 20

21.92 4.06 13

22.67 3.92 30

23.70 3.75 13

24.97 3.57 15

25.01 3.56 20

26.00 3.43 100

26.69 3.31 14

27.75 3.21 15

28.52 3.13 10

29.01 3.08 5

29.71 3.01 5

31.61 2.830 5

32.21 2.779 5

33.35 2.687 5

34.61 2.592 5

The table VI

Embodiment

The synthetic mixture, mol ratio 345

SiO ₂/Al ₂O ₃30.0 30.0 30.0

OH ^-/SiO ₂0.18 0.18 0.18

H ₂O/SiO ₂19.4 19.4 44.9

Na/SiO ₂0.18 0.18 0.18

R/SiO ₂0.35 0.35 0.35

Product composition %(weight)

SiO ₂64.3 68.5 74.5

Al ₂O ₃4.85 5.58 4.87

Na 0.08 0.05 0.01

N 2.40 2.33 2.12

Ash 77.1 77.3 78.2

SiO ₂/ Al ₂O ₃, mol ratio 22.5 20.9 26.0

Absorption, %(weight)

H ₂O 14.9 13.6 14.6

Hexanaphthene 12.5 12.2 13.6

Normal hexane 14.6 16.2 19.0

Surface-area m ²/ g 481 492 487

The table VII

BF ₃-promoted SiO ₂BF ₃-promoted zeolite

Alkylation temperature, ℃ 0 20 0 20

C ₅+ product, %(weight)

C ₅2.5 4.0 3.0 3.7

C ₆2.6 3.5 3.3 3.4

C ₇28.6 22.9 22.5 20.4

C ₈56.8 56.0 64.7 63.9

C ⁺ ₉9.4 13.6 6.4 8.6

TMP/DMH 2.2 1.6 2.2 1.6

Octane, feed gasoline

RON+O 93.2 86.8 93.5 88.4

MON+O 92.1 88.3 92.0 88.2

The table VIII

Alkylation conditions

Catalyzer invention invention HY HY

IC ₄/ 2-C ⁼ ₄Mol ratio 50 10 50 10

The hours 76 49 28 46 of logical steam

Transform (%) 95 73 99 85

Products distribution

C ₅1.5 0.6 1.8 1.7

C ₆4.9 3.4 5.0 3.3

C ₇3.9 2.2 7.1 5.7

C ₈74.4 63.1 43.0 36.0

C ⁺ ₉15.4 30.8 43.2 53.3

C ₈Products distribution

2,2,4-trimethylammonium amylalcohol 4.4 1.0 8.1 2.9

2,3,3-trimethylammonium amylalcohol 43.1 31.8 18.3 8.4

2,3,4-trimethylammonium amylalcohol 34.5 21.7 14.2 7.7

Dimethylhexane 16.3 25.3 56.6 69.7

Other product 1.8 20.3 2.8 11.2

Trimethylpentane/diformazan 5.0 2.2 0.7 0.3

Base hexane mol ratio

The table X

BF ₃-promoted SiO ₂BF ₃-promoted zeolite

Alkylation temperature, ℃

C ₅+ product, %(weight) 2.9 7.2 2.5 5.4

C ₅3.4 6.9 3.1 5.4

C ₆36.2 31.2 39.4 34.6

C ₇49.9 39.3 50.4 47.1

C ₈7.6 15.4 4.6 7.4

C ⁺ ₉2.0 1.4 2.2 1.6

TMP/DMH ^＊

Octane, feed gasoline

RON+O 93.9 90.7 95.5 91.5

MON+O 92.2 89.3 92.2 89.6

^*The TMP=trimethylpentane

The DMH=dimethylhexane

Table X IV

BF ₃-promoted SiO ₂BF ₃-promoted zeolite

Alkylation temperature, ℃ 0 20 0 20

C ₅+ product, %(weight)

C ₅4.9 7.0 4.3 6.4

C ₆4.5 4.7 3.4 4.5

C ₇4.1 5.3 3.4 4.9

C ₈77.9 71.9 83.5 77.7

C ⁺ ₉8.7 11.2 5.5 6.6

TMP/DMH 5.1 2.9 4.9 2.9

Octane, feed gasoline

RON+O 95.5 92.8 95.9 93.1

MON+O 93.1 91.7 94.2 93.1

Table X VI

BF ₃-promoted SiO ₂BF ₃-promoted zeolite

Alkylation temperature, ℃ 0 20 0 20

C ₅+ product, %(weight)

C ₅6.5 10.1 3.3 4.9

C ₆6.3 8.8 3.0 4.3

C ₇38.6 32.7 37.8 25.6

C ₈33.7 29.7 51.4 59.4

C ⁺ ₉14.8 18.7 4.6 5.9

TMP/DMH 4.1 2.1 5.4 3.0

Octane, feed gasoline

RON+O 92.9 90.5 93.2 93.3

MON+O 90.7 89.5 92.8 91.7

Table X VIII

BF ₃-promoted SiO ₂BF ₃-promoted zeolite

Alkylation temperature, ℃ 0 20 0 20

C ₅+ product, %(weight)

C ₅2.7 7.1 1.9 3.6

C ₆2.7 5.6 2.0 3.2

C ₇2.8 6.3 1.9 3.9

C ₈82.9 63.9 92.2 86.8

C ⁺ ₉8.9 17.2 2.0 2.6

TMP/DMH 5.9 2.8 6.7 3.4

Octane, feed gasoline

RON+O 97.3 93.2 98.2 94.8

MON+O 94.0 91.9 95.6 93.3

Table X IX

Embodiment 21 22 23 24

Catalyst B F ₃/ BF ₃/ BF ₃/ I/IBF ₃/

Zeolites Zeolites/H ₂O zeolite/H ₂O H ₂O

(no solid)

Live catalyst contains 0 10 10

The water yield, %(weight)

Temperature (℃) 10 10 20 20

Pressure P sig(Kpa) 150(1135 150(1135 150(1135 150(1135))))

BF ₃Speed (% of charging) 2.0 2.0 3.0 3.0

Feed olefin 2-butylene 2-butylene blended C ₃C ₄Blended C ₃C ₄

IC alkene charge ratio 10 10 10 10

Alkene WHSV 1.35 1.35 2.24 2.24

Olefin conversion (%) 57 100 100 100

Yield 1.2 2.0 2.0 2.2

The distribution of gross product (weight %)

C ₅1.4 2.5 5.4 8.2

C ₆2.6 2.6 5.4 7.9

C ₇1.4 2.8 34.6 33.1

C ₈22.9 85.9 47.1 41.6

C ⁺ ₉Total amount 71.7 6.2 7.4 9.1

RON+O 97.0 91.5 89.0

MON+O 93.0 89.6

Claims (15)

1, a kind of isoparaffin and alkene of making carries out the method that alkylation provides alkylate, it is characterized in that it is included under the alkylation conditions at zeolite as making isoparaffin and olefine reaction in the presence of the catalyzer, isoparaffin wherein contains 4-8 carbon atom, alkene contains 2-12 carbon atom, and this zeolite has the following X-ray diffracting spectrum of numerical value:

D-interplanar distance (A) relative intensity, I/Io＞100

12.36±0.4 M-VS

11.03±0.2 M-S

8.83±0.14 M-VS

6.18±0.12 M-VS

6.00±0.10 W-M

4.06±0.07 W-S

3.91±0.07 M-VS

3.42±0.06 VS

W=0～20 wherein

M=20～40

S=40～60

VS=60～100

2, method according to claim 1 is characterized in that its mesolite has the following X-ray diffracting spectrum of numerical value.

D-interplanar distance (A) relative intensity, I/Io * 100

30.0±2.2 W-M

22.1±1.3 W

12.36±0.4 M-VS

11.03±0.2 M-S

8.83±0.14 M-VS

6.18±0.12 M-VS

6.00±0.10 W-M

4.06±0.07 W-S

3.91±0.07 M-VS

3.42±0.06 VS

W=0～20 wherein

M＝20～40

S＝40～60

VS＝60～100

3, method according to claim 1 is characterized in that its mesolite has the following X-ray diffracting spectrum of numerical value.

D-interplanar distance (A) relative intensity, I/Io * 100

12.36±0.4 M-VS

11.03±0.2 M-S

8.83±0.14 M-VS

6.86±0.14 W-M

6.18±0.12 M-VS

6.00±0.10 W-M

5.54±0.10 W-M

4.92±0.09 W

4.64±0.08 W

4.41±0.08 W-M

4.25±0.08 W

4.10±0.07 W-S

4.06±0.07 W-S

3.91±0.07 M-VS

3.75±0.06 W-M

3.56±0.06 W-M

3.42±0.06 VS

3.30±0.05 W-M

3.20±0.05 W-M

3.14±0.05 W-M

3.07±0.05 W

2.99±0.05 W

2.82±0.05 W

2.78±0.05 W

2.68±0.05 W

2.59±0.05 W

W=0～20 wherein

M＝20～40

S＝40～60

VS＝60～100

4, method according to claim 1 is characterized in that its mesolite has the following X-ray diffracting spectrum of numerical value:

D-interplanar distance (A) relative intensity, I/Io * 100

30.0±2.2 W-M

22.1±1.3 W

12.36±0.4 M-VS

11.03±0.2 M-S

8.83±0.14 M-VS

6.86±0.14 W-M

6.18±0.12 M-VS

6.00±0.10 W-M

5.54±0.10 W-M

4.92±0.09 W

4.64±0.08 W

4.41±0.08 W-M

4.25±0.08 W

4.10±0.07 W-S

4.06±0.07 W-S

3.91±0.07 M-VS

3.75±0.06 W-M

3.56±0.06 W-M

3.42±0.06 VS

3.30±0.05 W-M

3.20±0.05 W-M

3.14±0.05 W-M

3.07±0.05 W

2.99±0.05 W

2.82±0.05 W

2.78±0.05 W

2.68±0.05 W

2.59±0.05 W

W=0～20 wherein

M＝20～40

S＝40～60

VS＝60～100

5, method according to claim 1 is characterized in that its mesolite has composition, and said composition comprises that the molar relationship formula is X ₂O ₃: (n) YO ₂, wherein n is at least 10, and X is a trivalent element, and Y is a quadrivalent element.

6, method according to claim 5 is characterized in that wherein X is an aluminium, and Y is a silicon.

7, method according to claim 1, the equilibrium adsorption ability that it is characterized in that its mesolite for cyclohexane vapor greater than 4.5%(weight), for the normal hexane steam greater than 10%(weight).

8, method according to claim 1 is characterized in that wherein isoparaffin is a Trimethylmethane, and alkene is propylene and/or butylene.

9, method according to claim 1 is characterized in that the mol ratio of wherein total isoparaffin and total alkene is 0.5: 1-500: 1.

10, method according to claim 9 is characterized in that the mol ratio of wherein total isoparaffin and total alkene is 3: 1-50: 1.

11, method according to claim 1 is characterized in that wherein the alkylated reaction temperature is-25 ℃-40 ℃, and the weight space-time speed of alkene is 0.01-100, and pressure is until 34580Kpa(5000psig).

12, method according to claim 1 is characterized in that its mesolite promotes with Lewis acid.

13, method according to claim 12 is characterized in that Lewis acid wherein is BF ₃

14, according to claim 12 or the described method of claim 4, it is characterized in that alkylated reaction temperature wherein is-40 ℃-250 ℃, the weight space-time speed of alkene is 0.01-100, pressure can be until 34580Kpa(5000psig).

15, method according to claim 1 is characterized in that alkylated reaction wherein carries out in the presence of water.

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