CN1060475A - The application of catalyzer in olefinic polymerization - Google Patents

Abstract

The invention discloses a kind of olefine polymerizing process, it is included in list-1-alkene is contacted with promotor with catalyzer.

Description

The application of catalyzer in olefinic polymerization

Invention relates to the application of catalyzer in olefinic polymerization.

The catalyzer that is loaded with chromic oxide is used for preparing olefin polymer at hydrocarbon solution or liquid slurry for a long time always, and products obtained therefrom all has good characteristic in many aspects.Extensively announce the technology of many kinds of carriers that are used for chromium oxide catalyst already, comprised silicon-dioxide, aluminum oxide, Thorotrast, zirconium white, oxidation sial and other refractory materials.But aspect putting into practice, have only silica support to be better than other and be successfully used to industrial production.Aluminum oxide is almost always listed among the suitable carrier, and it is an available, but productivity is extremely low.Comparatively outstanding carrier silicon-dioxide also has multiple shortcoming, and one of them is can not produce extra high molecular polymer during with sexavalent chrome.The purpose of this invention is to provide a kind of improved aluminum oxide.

Further aim of the present invention provides and a kind ofly can reach large-duty chrome catalysts.

Another object of the present invention provides a kind of chrome catalysts that can produce extra high molecular polymer.

Further object of the present invention provides a kind of being suitable for and starches the catalyzer that uses in the paradigmatic system at liquid.

It is to produce a kind ofly only just can to prepare the catalyzer that density range is 0.960～0.930 branched polyethylene with ethene that the present invention also has another purpose.

The present invention also has another purpose to provide molecular weight regulator H ₂Catalyzer with wide sensitive range, its sensitive range from insensitivity almost to height susceptibility.

It is that preparation is used for the high molecular of film and blowing and the tight bifurcation mixture of low-molecular weight polymer that the present invention also has another purpose.

It is to overcome traditionally to do the difficulty that carrier causes with aluminum oxide and silicon oxide in the chromium catalysis in olefine polymerization that the present invention also has another purpose.

One aspect of the present invention provides a kind of aluminium oxide silicide, and aluminum oxide wherein also can be fluoridized and/or phosphorylation.

B the present invention will fluoridize and/or the aluminium oxide silicide carrier is used for the chrome catalysts of olefinic polymerization.

According to another aspect of the present invention, aluminum phosphate forms in the hole of aluminum oxide.

Being briefly described as follows of accompanying drawing of the present invention:

Fig. 1 represents with the density of the ultrahigh molecular weight polyethylene(UHMWPE) polymkeric substance of various catalyst system preparations and the relation between the melt viscosity.

Fig. 2 represents the relation between density polymer and the limiting viscosity.

According to the present invention, select to carry out the surface-treated aluminium oxide and also can contain small amount, but the quality of final catalyst is not had other component of adverse influence. But say that generally this aluminium oxide is pure on substantially. Aluminium oxide can prepare by known technology. For example, by the sodium aluminate of alkalescence and acid reacting aluminum sulfate, or use alkali, such as ammonia or ammonium hydroxide, in aluminium salt, perhaps pass through flame hydrolysis. If need, can be before processing the calcination aluminium oxide, as in air, under 300～900 ℃ of temperature, heating, preferably 500 to 800 ℃. But whether calcination is not main.

The fluorine amount of chemical combination, take the weight of aluminium oxide as benchmark, general fluorine-containing weight is 0.1～5%, best 0.5～3%.

The preparation of surface siliconization aluminium oxide is to contact with aluminium oxide with a kind of silication agent, normally forms aluminium oxide liquid slurry in a kind of solution of silication agent. Generally make solvent with low-carbon alcohols, as contain 1 to 6 carbon atom alcohol. Aluminium oxide is with after this solution mixes, with the compound drying that obtains. Another kind method is that the steam of aluminium oxide with the silication agent is contacted. The consumption of silication agent, take the weight of aluminium oxide as benchmark, the silica of 0.2～20% weight is preferably 0.5～10%. Resulting product is the aluminium oxide with silicon dioxide meter finishing coat, and these are different from silica one aluminium oxide commonly used.

Resulting this new product is suitable for doing catalyst carrier, but also is widely used in using the occasion of aluminium oxide.

" silication agent " word means and comprises silicon alkoxide salt, fragrant and mellow silicon salt and hydrolysate thereof, and for example: oxyalkylsiloxane when for activated carrier or catalyst it being calcined, can obtain high-purity, high temperature oxidation resisting silicon. The example of this compounds comprises tetramethoxy-silicane, tetraethoxysilane (tetraethylorthosilicise), four (2-ethyl butoxy) silane, four (2-methoxy ethoxy) silane, tetraphenoxy-silicane alkane, phenyl triethoxysilane and their hydrolysate and mixture etc. At present preferably silication agent is made up of a kind of polymer siloxane type of tetraethoxysilane, and wherein containing and being equivalent to weight is 40% silica. The trade names of this constituent are Silbond

(registered), by Connecticut, USA, Xi Gang (Westport), Si Tuofo chemical company sells.

The silication agent can be transformed into surface silica dioxide after calcination processing described above, the aluminium oxide that maybe will process is placed, until the inorganic agent hydrolysis is transformed into silica.

According to another embodiment, aluminium oxide is processed with fluorization agent, fluorine is combined on the aluminium oxide, and makes the carrier for the Cr VI catalyst, it and co-catalyst share, or as the carrier of Organic Chromium catalyst. Fluorization agent is two ammonium hydrogen difluorides preferably, NH₄HF ₂ Silicon fluoride ammonium (NH₄） ₂SiF ₆, also be suitable for. The silicon fluoride ammonium is both siliceous, and is also fluorine-containing, and the back also will be spoken of, and silication and the combination of fluoridizing belong to scope of the present invention, outside the silicon fluoride ammonium defluorination probably no longer with other material effect because when heating silicon lost. Fluorization agent can with aluminium oxide chemical combination in any suitable manner, but generally be to realize by in the solution of fluorization agent and a kind of suitable solvent such as alcohol or water, forming aluminium oxide liquid slurry. Carbon atom is very suitable once the alcohol to three, because of their volatility and low surface tension. For obtaining required fluorine concentration in the dry afterwards compound, it is an amount of that used solution is wanted, and drying can realize by conventional method, such as evaporation or vacuum drying after the suction strainer. Use comparatively speaking volatile solvent, such as methyl alcohol, then can adopt the condition of relative mitigation, such as 100 ℃ or lower.

Also can be used in combination to fluoridize with silication and obtain F-si/Al₂o ₃ In this case, preferably at first add fluorization agent, be preferably in before the adding silication agent, add fluorization agent, then dry. This is because add the rear fluorization agent of afterwards adding of silication agent and/or chromium and can cause undesirable precipitation in some cases. But it is all feasible to add these combinations with any order.

If need, fluorided alumina, aluminium oxide silicide or fluoridize aluminium oxide silicide and can further process with phosphoric acid agent or phosphitylation agent add after the chromium, obtain containing the system of five components, i.e. P-F-si-Cr/Al₂O ₃ For example, the carrier of this phosphorylation or phosphitylation can be P-F-si/Al₂O ₃，P-F/Al ₂O ₃Or P-si/Al₂O ₃ If usually fluoridize or also use phosphoric acid agent or phosphitylation agent silication the time, then at first carry out phosphorus and process.

Phosphoric acid agent or phosphitylation agent can be put into a kind of organic liquid such as the alcohol miscible with water, process hydrogel or xerogel with it then. If raw material is hydrogel, then organic liquid and phosphoric acid agent constituent can make hydrogel be transformed into xerogel, also can reach needed phosphorylation or phosphitylation degree. More particularly, if use hydrogel, available water is washed it, and then, with the organic liquid of phosphoric acid or phosphitylation agent such as phosphoric acid or phosphorous acid, such as isoamyl alcohol or methyl alcohol, washing is then filtered, and solvent is evaporated. In addition, the also steam treatment of phosphoric acid agent or phosphitylation agent of alumina gel.

During the reaction of phosphoric acid agent or phosphitylation agent and aluminum oxide, its consumption make the P/AL atomic ratio on product surface be 0.01: 1 to 0.3: 1 better, be preferably 0.05: 1 to 0.2: 1.But actually, can use as required phosphoric acid agent or phosphitylation agent, just after phosphorylation or phosphitylation are finished dealing with, wash excessive part simply off and get final product.When usually aluminum oxide being carried out the processing of phosphorylation or phosphitylation, aluminum oxide is in advance in air, under 300 ℃ to the 700 ℃ temperature through the calcining, phosphorylation or phosphitylation are handled and are generally carried out under 15 ℃～500 ℃ temperature, if use phosphoric acid salt or phosphite solution, temperature is preferably the boiling point of room temperature to solvent; If use steam is preferably about 200 ℃, the time is 1 minute to 2 hours, preferably 2 minutes to 30 minutes.General phosphoric acid (the H that adopts ₃PO ₄) methanol solution.

In other words, the add-on of phosphorous component adds up to benchmark with the mol of aluminium, and the molar percent that reach the bonded phosphorus compound is 1 to 30%, and preferably 5 to 20%.Usually, be 100 to 3000 to the scope of the phosphorus atom ratio of each atom percent chromium, preferably 500 to 2000.Concerning surface-area, the amount of the phosphorus compound that obtains with phosphoric acid agent will be enough to make the phosphorus content on the alumina surface to be about 0.005 to 1 milligram of phosphorus/rice ², preferably be about 0.01 to 0.5 milligram of phosphorus/rice ², measure by BET nitrogen absorption method.

With regard to the type of chromium cpd of the present invention, the content of two aspects is arranged, first aspect: chromium cpd can be the compound that any hexavalent state maybe can be converted into hexavalent state, and can whenever add before activation.The general range of this catalyzer chrome content is that the weight of the alumina supporter of the processing of crossing with drying is benchmark, be about 0.001% to 10%, be preferably 0.1%～5%, preferably be about 1%, perhaps say so, because the amount of bonded treatment agent is less relatively, it then is benchmark with the aluminum oxide, the weight percentage of chrome content is 0.001～10% in the catalyzer, is preferably 0.1～5%, preferably is about 1%.With chromium cpd bonded technology is known.For example, with the hydrocarbon solution of a kind of material such as chromic acid tertiary butyl ester, the dipping xerogel; Perhaps, with chromium cpd, as CrO ₃The aqueous solution of (chromium trioxide) chromium acetate or chromium nitrate is added on the dry hydrogel before; Or chromium and aluminum oxide carry out co-precipitation.Chromatize is preferably in after fluorochemical processing and the phosphorus processing.

The activation temperature of this chromium-containing catalyst can be lower than with the silicon oxide activation temperature of the common usefulness of chromium-containing catalyst that is carrier.Suitable temperature is 300～900 ℃.It better is 500～800 ℃.The activation environment can be any well-oxygenated environment, but for convenient, generally uses air.Time is 1 minute to 48 hours, and 0.5 to 10 hour preferably.Also can before handling, adopt back activatory similarity condition that aluminum oxide is carried out precalcining if desired.

A second aspect of the present invention content is about the chromium cpd type, can use the organo-chromium compound of chromium valency less than its maximum valency.Certainly, organic chromium described here also can be used for as the chromium source, being transformed into sexavalent chrome through calcining in the first aspect.At this on the one hand, organic chromium is after carrier carries out high-temperature activation, rather than adds before.The described carrier of activation second aspect content can adopt with in first aspect, temperature that deactivated catalyst is identical and environment.But its temperature can have bigger deviation, and the temperature of activated carrier is low to moderate 150 ℃ before adding chromium, all is feasible up to 1000 ℃.Organo-chromium compound can comprise zerovalent compound, and as the chromium complex of π keyed jointing, for example, diisopropylbenzene(DIPB) closes chromium or dibenzene-chromium.The United States Patent (USP) 3,976,632 of the Di Laipu that on August 24th, 1976 published quite at length discloses the zerovalent chromium compound of this class π keyed jointing.Here with its disclosure as reference.The divalence organo-chromium compound also is suitable for, and as Chromocene, i.e. two (cyclopentadienyl) chromium (II), and substitutive derivative has one or more substituting groups on the cyclopentadienyl rings of this derivative.

The advantage of Chromocene is that high-density, extra high molecular polymer can be provided.Organo-chromium compound is stated from the aluminum oxide of handling the influence to hydrogen and also tends to special susceptibility, thereby allowing is having bigger handiness aspect the control molecular weight, because catalyzer trends towards providing the ultra-high molecular weight compound, and to the hydrogen sensitivity, this just may have the polymkeric substance of wide spectrum molecular weight with a kind of Catalyst Production.

At present preferably organo-chromium compound be following formula I or formula II the two one of:

(I) Cr(R) ⁿ(II) Crx(R) ₂X wherein n equals 3 or 4; X equals 3 or greater than 3; R is-CH ₂MR ' R " R

, wherein M is the 4th main group element, i.e. c, Si, Ge, Sn or Pb; To a given compound, the R base is identical, R ' R " or R Be identical or different (preferably identical), contain the aliphatics or the aromatic hydrocarbyl of maximum 10 carbon atoms approximately, preferably contain the alkyl of 4 carbon atoms.Wherein also comprise the combination group, as alkaryl.The formula I compound is preferably; Cr (CH ₂Si(CH ₃) ₃) ₄, wherein m is Si, R ', R " and R

Be methyl (CH ₃), n is 4, i.e. four (trimethyl silane methyl) chromium (IV).To formula II, compound is a tetramer preferably, (Cr ₄(CH ₂Si(CH ₃) ₃) ₈, wherein m is Si, R ', R " and R

Be methyl (CH ₃), x equals 2, i.e. eight (μ-trimethyl silane methyl) four chromium (II).

Another kind of suitable formula II compound comprises: eight (benzyl dimethyl-silane methyl) four chromium and eight (allyl dimethyl base silane methyl), four chromium.These compounds be stated from according to the present invention demonstrate on the aluminum oxide of processing significant really active and also responsive really to the effect of hydrogen.

Can also use the mixture of two or more chromium component.For example, chromium (+6)-chromium (0); Chromium (+6)-chromium (+2); Chromium (+2)-chromium (0), or use two kinds of different chromium (0) component, or two kinds of different chromium (+2) component, or a kind of chromium (0) component and a kind of chromium (+2) component.It is most suitable to select two components to use from chromium (0) and chromium (+2).

Also can mix and use various catalyzer, a kind of catalyzer promptly of the present invention and chromium or the vanadium that is stated from the silicon-dioxide commonly used, perhaps be stated from aluminum phosphate on chromium or vanadium combine, or combine with titanium or zirconium system.

The amount of organo-chromium compound is about 0.02 millimole chromium cpd to about 5 millimole chromium cpds to every gram carrier.

Another embodiment of the invention is called " being that the hole is cogelled ", for simplicity, can adopt any carrier of handling described here, makes phosphaljel formation and becomes porose.According to this programme,, in the liquid that contains phosphate ion and a kind of aluminium salt, then add neutralizing agent and form gel the aluminum oxide dipping of handling.The carrier of treated mistake is before this dipping, and it is described to activate problem as discussed earlier, should be preferably in 500～800 ℃ in 300～900 ℃ of temperature lower calcinations.If the constituent of Xing Chenging is as the catalyzer basis thus, for example as the carrier of chromium, so this catalyzer can add without calcining, or before phosphaljel forms, in carrying out, or adds afterwards.The aluminium component is aluminum nitrate preferably, but aluminum chloride or other aluminium salt all can use.The phosphate ion ortho-phosphoric acid of preferably originating, primary ammonium phosphate and Secondary ammonium phosphate etc. also can use.Common used liquid is water, though also available polar organic solvent.The another kind of selection is to use undressed alumina supporter, and phosphatic formation plays the processing effect, thereby, also just activated common inactive aluminum oxide.

The antacid reagent of any energy all can use, as dense ammonium hydroxide, ammonia, perhaps be dissolved in the alcohol or the alkali such as ammonia in other non-aqueous solvent all better, also can use volatile salt, oxyethane, propylene oxide.The add-on of neutralizing agent will make gelation process reach less amount immediately.And make gelation process continue to reach one hour.

Porose cogelled last processing used water of making and/or alcohol wash or do not wash.If this porose cogelled carrier as catalyst component (as chromium cpd), it can provide a kind of dual-component catalyst of tight formation, rather than mixture or single composition.

General and the promotor of sexavalent chrome catalyzer of the present invention uses jointly.Suitable promotor comprises organoaluminum and organoboron compound.Only boron compound is the trialkyl boron compound, three normal-butyl borines particularly, tripropyl borine and boron triethyl (TEB).Other suitable boron compound comprises trialkylboron compound widely, particularly contains the compound of 1 to 12 carbon atom alkyl, preferably contains 2 to 5 carbon atoms, and triarylboron, for example triphenylborane; Also available boron alkyl alkoxide, as: B(C ₂H ₅) ₂OC ₂H ₅; The haloalkyl boron compound is as BC ₂H ₅CL ₂The alkylaluminium cpd that share comprises R 4 ₈AL, R 4 ₂ALX and R ⁴ALX ₂Compound, wherein R ⁴Be the alkyl of 1 to 12 carbon atom, X is a halogen, and it is suitable especially to be preferably chlorine, triethyl aluminum and diethyl aluminum muriate.

The amount of the promotor that uses is 0.2/1000000th to 25 part to solvent for use in the system or thinner, is preferably 0.2 to 10 part.If without solvent or thinner, then promotor will be immersed on the catalyzer, and its amount will make promotor: the mole ratio of chromium (atom) is 0.5: 1 to 5: 1.In using solvent and diluent system according to the chromium amount in the catalyzer, the consumption of promotor boron or aluminium will be 0.01 to 3 times of weight of chromium, it better is 0.1 to 2 times, identical with the weight multiple of chromium, if according to used boron of every atom percent chromium or aluminium atomicity are calculated, the consumption of promotor will make every atom percent chromium that 0.05 to 14 boron atom or aluminium atom are arranged approximately, preferably is about 0.5 to 10 boron atom or aluminium atom.

Promotor or elder generation and catalyst premixing are perhaps introduced reactor as an independent component, and the latter is more excellent program.

When certainly, using final catalyzer also can with or contain the component that other does not influence this catalyst performance.For example, other promotor, the static inhibitor in the polymeric layer, and other component commonly used.

Catalyzer of the present invention can be used for list-1-alkene that at least a per molecule of polymerization contains 2 to 8 carbon atoms, preferably ethene, propylene, 1-butylene, 1-amylene, 1-hexene and 1-octene.The present invention is specially adapted to from the mixture of ethene to produce Alathon and multipolymer, and mixture contains percent 0.5 and contains one or more comonomers of selecting the 1-alkene of 3 to 8 carbon atoms to 20 mol from per molecule.Typical comonomer comprises aliphatics 1-alkene, as propylene, and 1-butylene, the 1-amylene, the 1-hexene, 1-octene and other be the alkene of long-chain more, and conjugation or non-conjugated diene hydrocarbon, as 1,3-butadiene, isoprene, piperylene, 2,3-dimethyl-1, the 3-divinyl, 1,4-pentadiene, 1,5-hexadiene, and other similar diolefine and their mixture.Ethylene copolymer contains weight at least and is about 90%, better is about 97% to 99.6% polymeric ethylene unit.To ethene, propylene, 1-butylene, 1-amylene and 1-hexene are extraordinary comonomers.

Utilize common equipment and contact process, by the slurry polymerization of solution polymerization, liquid and vapour phase polymerization technology by these compounds of Preparation of Catalyst of the present invention.Between monomer and monomer and contacting of catalyzer can realize by arbitrary mode of known solid phase catalyst technology.A kind of method easily is that catalyzer is suspended in the organic medium, and stirs the mixture in whole polymerization process, is in suspended state to keep catalyzer.Other known contact method also can adopt as fluidized bed, gravity bed and fixed bed.Catalyzer of the present invention also can be used for producing granular polyvinyl process, as the United States Patent (USP) 3,624,063 of the Witter (Witt) of announcing on November 30th, 1971, the published content of this patent at this as reference.

The catalyzer of foregoing invention is particularly suitable for the polymerization of liquid slurry.Liquid slurry process is generally carried out in a kind of inert diluent (medium), as paraffin wax (paraffins), cycloalkanes or aromatic hydrocarbons.For main ethene polymers, adopt temperature to be about 66～110 ℃.The variation range of granular pressure process is about 110 to 700(pound/inch ²) pounds per square inch absolute (psia) (0.76～4.8 megabar) or higher.Catalyzer keeps suspending, and under sufficiently high pressure, contact with monomer or multiple monomer, to keep medium and at least a portion monomer or multiple monomer among liquid phase, it is solid particulate that selected medium and temperature will make the polymkeric substance of generation, and collects with this form.Generally making Alathon or be mainly in the liquid slurry polymerization system of multipolymer of ethene, suitable temperature range is 150～230 °F (66～110 ℃).

When using catalyzer to carry out polymerization according to second aspect present invention, chromium cpd and carrier can add reactor respectively.Another kind of way, special in reactor large-scale, continuous operation, can as mixed carrier and chromium cpd in the n-hexane, periodically add this mixture then as required in advance at inert diluent to keep the required speed of polyreaction.

The concentration of catalyzer (chromium cpd+carrier) can count 0.001 percent to one of about percentage (weight) by the tara of reactor.

When using hydrogen in the prior art, pressure generally reaches 120 pounds per square inch absolute (psia) (pound/inch ²) (0.8 megabar), scope is 20～70 pounds per square inch absolute (psia) (pound/inch preferably ²) (0.01～0.48 megabar).Similarly the hydrogen amount also can be used for the present invention, though because catalyst system of the present invention to the susceptibility of hydrogen, would rather be used lower pressure when with organic chromium.As from the mole number of thinner being calculated the mole percent of hydrogen, the concentration of hydrogen can be about 0.1～10 mol %, is preferably 0.2 to 1.25 mol %, preferably is about 1 mol %.

The carrier that adopts in each example and for confirmatory experiment comprises Davison 952 silicon-dioxide and according to United States Patent (USP) 4,364, the ALPO of 841 preparations ₄To experiment of the present invention, adopt the high pore volume of Davison HPV() AL ₂O ₃With Ketjen B AL ₂O ₃

Example 1

Contain the catalyzer and the high pore volume of vinyl polymerization (HPV) aluminum oxide of eight (μ-trimethyl silane methyl) four chromium (II), surface-area is 530 meters approximately ²/ gram, pore volume are 2.7 milliliters/gram (B.E.T) approximately.After the processing, every part of used aluminum oxide all in dry air, under 600 ℃ of temperature through calcining 3 hours.

Comparative catalyst A (is abbreviated as Cr by eight (μ-trimethyl silane methyl) four chromium (II) of burnt unmodified aluminum oxide and common every gram carrier 0.1 millimole of using ₄(Tms) ₈) form.Cr ₄(Lms) ₈Be a kind of new compound, it prepares shown in example 13.

The catalyst B of being invented is by-aluminium oxide silicide with the Cr of same amount in the catalyst A ₄(Tms) ₈Form.Aluminum oxide Silbond ₄₀ The methanol solution silication, contain 3.2%(weight) SiO ₂, introduced as following catalyzer D.

The catalyzer C that is invented is by fluorided alumina with the same Cr that measures of every gram carrier in the catalyst A ₄(Tms) ₈Form.NH with q.s ₄HF ₂Impregnated alumina prepares fluorinated support in excessive methanol, makes in the exsiccant constituent, and the weight content of the chemically combined fluorine that calculates with F is after 1.5% dipping, this mixture in vacuum oven under 80 ℃ of conditions dry 12 hours.Product sieves by 35 sieve meshes, and a copy of it is pressed aforementioned at 600 ℃ of temperature lower calcinations, and obtains the carrier of modification.

The catalyzer D that is invented is by the Cr that fluoridizes aluminium oxide silicide and measure equally with catalyst A and B ₄(Tms) ₈And form.The preparation of modified support is the NH with aluminum oxide and q.s ₄HF ₂Methanol solution and Silbond ₄₀ Mix mutually, in the siccative of making, F and SiO ₂Weight content be respectively 1.5% and 3.2%.As described above after the drying, with product screening and calcining.

Being aggregated in the 2 liter stainless steel stirred reactors of ethene carried out, and temperature is 95 ℃, every part of carrier 30 as one kind milligram, and as above-mentioned proper C r ₄(Tms) ₈After carrier is put into reactor, inject Cr separately ₄(Tms) ₈This reactor is equipped with 1.25 pounds of (567 gram) Trimethylmethanes makees thinner.To catalyst A and B, each experiment was carried out 1 hour, and to catalyzer C and D, each experiment is 30 minutes, and reactor general pressure (thinner adds ethene) is about 565 pounds per square inch absolute (psia) (pound/inch ²).From pressurized reservoir, supply with ethene as required, to keep above-mentioned pressure.

Find from experiment, the polyethylene that comparative catalyst A produces, it calculates productive rate and restrains polymkeric substance for every gram carrier 270 per hour.The polymer property undetermined.

The polymkeric substance that the catalyst B of being invented is produced, its productive rate is 800 gram/Grams Per Hours.

The polyethylene that the catalyzer C that invented under the contrast produces, it calculates productive rate and is every gram carrier 12 per hour, and 000 gram polymkeric substance, this polymkeric substance have/10 minutes high-load melting index (HLMI) of 1.4 grams, press ASTMD1238, condition F mensuration.

The polyethylene that the catalyzer D that invented generates, it calculates productive rate and is every gram carrier 13,500 gram polymkeric substance per hour, and HLMI 0.4 restrains/10 minutes.

Obviously, add silication and cause catalyst activity significantly to increase just because of fluoridizing and fluoridizing, though only can be directed at some improvement with siliconizing to the modification of aluminum oxide.The results are shown in the table I.

The table I

Calculated productive rate gram/Grams Per Hour

A contrasts AL ₂O ₃270

B invents Si-AL ₂O ₃800

C invents F-AL ₂O ₃12,000

D invents F-Si-AL ₂O ₃13,500

Example 2

Two (cyclopentadienyl) chromium II (Chromocene) catalyzer and vinyl polymerization

Prepare a pair of catalyzer, with the specified drying of two (cyclopentadiene) chromium (II) solution impregnation that is dissolved in the paraffin wax (as normal heptane), through the incinerating carrier, the chromium amount will enough make and add that in siccative weight is 2% chromium.Used carrier is that high pore volume aluminum oxide also is 3.0% SiO with same aluminum oxide weight content ₂With 1.5% F dipping, this two kinds of equal dryings of aluminum oxide and in dry air, 700 ℃ of temperature lower calcinations 3 hours.

Get each portion of every kind of catalyzer and all be used for foregoing vinyl polymerization.Its result is shown in the table II.

The table II

Carry out vinyl polymerization with the carrier that is loaded with two (cyclopentadienyl) chromium.

90 ℃ of temperature, no hydrogen

Polymkeric substance

The experiment number

Carrier

Calculating productive rate gram/gram catalyzer/40 minutes

Reaction times minute

The output gram

(b) limiting viscosity deciliter/gram

(c) density grams per milliliter

Annotate

1

Aluminum oxide

300 （a）

60

18

－

－

Contrast

2

The F-Si-aluminum oxide

3170

40

204

27

0.9257

Invention

(a) the actual experiment time is 60 minutes, and calculating productive rate at this moment is 500 gram polymkeric substance/gram catalyzer.It is linear in time that productive rate is calculated in design, and then 40 minutes calculating productive rate is: 500 * 40 ÷ 60 equal 330.

(b) limiting viscosity is to measure according to ASTM D-4020-81, improves and uses 0.015%(weight) dissolved polymers, and without 0.05%(weight).This change is to make to be difficult for dissolved polymers and can to dissolve better.At present, regulation ultrahigh molecular weight polyethylene(UHMWPE) (UHMWPE) has about 20 or higher limiting viscosity.

（c）ASTM D-1505

In the table II, the low-yield result of experiment 1 shows that in the control experiment 1, two on the unmodified aluminum oxide (cyclopentadiene) aluminium is active low catalyzer comparatively speaking.Experiment 2 catalyzer of being invented have more activity, and can prepare ultrahigh molecular weight polyethylene(UHMWPE).

Example 3

Aluminium oxide silicide-sexavalent chrome catalyzer and vinyl polymerization

Silbond with q.s ₄₀

Organic silicic acid salts solution and hydration chromic salts (Cr(NO ₃) ₈9H ₂O or Cr(C ₂H ₃O ₂) ₃H ₂O) in methyl alcohol, floods AL ₂O ₃Preparation band SiO ₂The high pore volume aluminum oxide series catalyzer of top coat, every kind of making constituent all contains 2.0%(weight) sexavalent chrome (by oxide compound), SiO ₂Amount change, all calculated amount are all calculated by vacuum-drying, burnt product.Each product under 700 ℃ of temperature, is calcined and was activated in 3 hours all in dry air.

Ethene polymers as previously mentioned, weight according to isobutane diluent, add 1.0 milliliters of boron triethyls (TEB) as promotor in the polymerization, 0.5%(weight for normal hexane), be equivalent to about 8ppmTEB by isobutane diluent, the catalyzer that also adds a certain amount of activation, the catalyst weight scope is from about 0.05 to 0.15 gram in this series.

Used condition is shown in gained result and the table III

(a) suppose with the time cycle linearly, then 45 minutes being proofreaied and correct is 30 minutes, and productive rate was in promptly per 30 minutes:

(1130 * 30)/45=750 gram

(b) suppose that linear with the time cycle, it is 30 minutes that 20 minute reaction times was proofreaied and correct with to annotate (a) same, productive rate was in promptly per 30 minutes:

(1390 * 30)/20=2080 gram

(c) use Silbond ₄₀The solution impregnation aluminum oxide prepares catalyzer, and aluminum oxide is in advance 700 ℃ of temperature lower calcinations 3 hours.

(d) CrO of usefulness q.s ₃With water retting HPV aluminum oxide, the preparation comparative catalyst, its chromium content will reach 1%(weight on burnt catalyzer).Catalyzer is in dry air, and activation (calcining) is 3 hours under 700 ℃ of temperature.

(e) it is the same to suppose to annotate (a) together, linear with the time cycle, and it is 30 minutes that 60 minute reaction times was proofreaied and correct, and productive rate was in promptly per 30 minutes:

(500 * 30)/60=250 gram

Comparative catalyst in the experiment 8 of table III was produced 250 grams in per 30 minutes approximately, and this is to be stated from resulting typical consequence on the unmodified aluminum oxide with sexavalent chrome.

Test 1～7 data as can be seen from the present invention of table III, in each case, all make activated catalyzer.The catalyst activity that contains 8% silicon-dioxide (weight) in the experiment 4,5 approximately is best.

The productive rate numerical value of testing in 3 and 7 is compared, and wherein every kind of catalyzer all contains 5.4% the silicon-dioxide (weight) of having an appointment.Obviously, in mixed silica (experiment 7) before, the precalcining aluminum oxide can obtain active higher catalyzer, is higher than the catalyzer that adds silicon-dioxide in the aluminum oxide that contains volatile matter (wetting).Productive rate is the twice of experiment 3 approximately.

By the rheology spectrum, under 230 ℃ of temperature, adopt the parallel plate geometry structure, obtain the melt viscosity data.Strain amplitude 5%, sample chamber nitrogen, vibration frequency range is 0.1 to 500 radian per second.The data of gained show that storage modulus and out-of-phase modulus are the function of vibrational frequency.Published by Willie (Wiley) as 1961, not auspicious to show " viscoelastic property of polymkeric substance " chapter 1 described, can calculate dynamic complex viscosity (η successively by these data ^*).Institute's value direct correlation polymericular weight, this value is big more, and molecular weight is big more.Show (the η of industrial ultrahigh molecular weight polyethylene(UHMWPE) (UHMWPE) ^*) value is about 30 megapoises, condition determination is 190 ℃, 0.1 radian per second.

The polymkeric substance of producing in the experiment 1 of the present invention has melt viscosity 38 megapoises, can be included into the UHMWPE class.

Example 4

Fluorided alumina-sexavalence Cr catalyzer and vinyl polymerization

With enough Cr(NO ₃) ₃9H ₂O methanol solution impregnated alumina, preparation contains the catalyst series of bonded fluorine and high pore volume aluminum oxide, making dry catalyst Cr is 1.5%(weight) calculating content.Then with resulting mixture drying; Use the NH of q.s again ₄HF ₂Methanol solution flood this mixture, obtain based on bonded fluorine dry catalyst, certainweight per-cent, for being used for polymerization, every kind of catalyzer carries out calcining and activating in dry air under specific time and temperature.

In this example, repeat to show control experiment 8 in the III.

Under 85 ℃ of temperature, the same manner by example 3 carries out vinyl polymerization with every kind of catalyzer and 8ppmTEB promotor.

Used condition and gained result list the table IV in.

The table IV

Use Cr ^{+ 6}-fluoridize AL ₂O ₃Catalyzer and TEB promotor carry out vinyl polymerization, and stagnation pressure is 565 absolute pressure (pound/inch ²)

(a) annotate in the III as described in a, b, the e as table, it was proofreaied and correct to 30 minute reaction times.According to the value in the arc is the calculating productive rate of real reaction time.

From the data of the experiment of the present invention 1-4 of table IV, the productive rate numeric ratio that yield results and control experiment 8 are obtained shows that all the catalyzer that is made by the fluorizated aluminum oxide has more activity.In other words through fluoridation, productive rate increases to 8.7 times from 3.8 approximately, contains the 2.7%(weight of having an appointment) the catalyst activity maximum of bonded fluorine.Resulting extra high molecular polymer has melt viscosity 40 to 50.

Experiment 1 shows that further very a spot of F is a produce effects, and experiment 5 shows, when the F amount surpasses 3%(weight) time, catalytic activity significantly reduces.Consider that such as other factorses such as surface-area 5% is considered to the useful maximum value of possibility, generally say, the 3%th, the upper limit.

Example 5

Silication, fluorided alumina-sexavalence Cr catalyzer and vinyl polymerization

Use Silbond ₄₀

As the source of silicon-dioxide, (NH ₄) ₂SiF ₆Or NH ₄HF ₂As the source of fluorochemical, Cr(C ₂H ₃O ₂) ₃H ₂O or Cr(NO ₃) ₃9H ₂O is as the source of Cr, and according to the aforementioned manner impregnated alumina, preparation contains the catalyst series of bonded fluorine, silicon-dioxide and high pore volume aluminum oxide, then every kind of mixture is heated in dry air, through certain hour, dry and activation (calcining) is used for polymerization.

As before, with every kind of catalyzer and 8.3ppmTEB or TEA(triethyl aluminum, in an example) promotor carries out vinyl polymerization, and an experiment is arranged, and carries out having in the presence of 5 milliliters of 1-hexenes and the hydrogen.

Used condition and the result who obtains are illustrated by the table V.

Table V C r ^{+ 6}A L is fluoridized in-silication ₂O ₃Be catalyzer, T E B or TEA are the promotor vinyl polymerization, and stagnation pressure was 565 pounds per square inch absolute (psia) (pound/times ²)

The experiment number	Calculated amount %(weight)			Temperature ℃		Reaction times minute	Calculated the productive rate gram/30 minutes	Polymkeric substance
											Si?O 2	F	C?r	Activation	Reaction	The output gram	HLMI	The melt viscosity megapoise
	（a) 1	0	0	2.0	700			96	60	250									46	(b) -	-
2						1.0	1.8				1.5	600	85	30	945	135	0	43
	3	1.3	2.6	1.5	600			85	30	2000									140	0	54
(c) 4						1.3	2.6				1.5	600	100	25	900(750)	35	0.8	-
	(d) 5	1.6	3.2	1.5	600			85	20	(f) 120(80)									8	-	-
6						2.5	2.0				2.0	700	85	30	2410	170	0	55

(e) 7	4.0	2.2	1.5	700	85	30	1440	105	0	39
											8	4.0	2.2	1.5	750	85	30	1300	98	0	-
9	2.5	2.7	1.5	700	85	30	1015	150	0	-
											10	3.2	2.2	4.0	700	85	30	2100	160	0	-
11	4.8	2.2	1.5	700	85	30	2380	129	0	-

(a) with the experiment 8 of showing III.

(b) dash is represented not measure.

(c) use 5.0 milliliters of 1-hexenes, 50 pounds/inch in the experiment ²Hydrogen.The productive rate that calculates is equally proofreaied and correct to 30 minute reaction times with the form of front, and parenthetic value was 750/25 minute reaction times of gram.

(d) correction calculation productive rate to the 30 minute reaction times, parenthetic value is 20 minute reaction times 80 grams.

(e) use 8.5ppmTEA to be promotor, the experiment that other was is a promotor with 8.3ppmTEB all.

(f) obvious, this catalyzer has reduced activity by accident.

The result that observation table IV example goes out can find out, based on zero HLMI result, under no hydrogen situation, vinyl polymerization is become very high-molecular weight homopolymer.To this, catalyzer of the present invention is activated among the experiment 2-11.Melt viscosity value shown in the experiment 2,3,6,7 is 43,54,55,39 megapoises, and these values are considered to indicate ultrahigh molecular weight polyethylene(UHMWPE).The quite insensitive catalyzer of pair hydrogen is also arranged, as test shown in 4, the HLMI of prepared ethene/1-hexene copolymer is 0.8.This value indicates a kind of high-molecular weight polymer.Per 30 minutes, the low-yield of every gram catalyzer 120 gram polymkeric substance was considered to abnormal results.This catalyzer obviously loses activity, perhaps owing in its preparation or polymerization process, contacted Toxic unintentionally.

Example 6

Use separately silication, fluorided alumina-sexavalent chrome catalyzer, and use with sexavalent chrome-aluminate or phosphate catalyzer, in amplification test, produce ethene polymers.

Prepare several silication with mode as described above, fluoridize high pore volume aluminum oxide-sexavalent chrome catalyzer.The one example is to use Silbond ₄₀ And Cr(NO ₃) ₃9H ₂O Virahol under handle aluminum oxide, then with mixture in vacuum oven, dried overnight under 80 ℃ of temperature, second day with solid phase prod and NH ₄HF ₂And methanol mixed, and equally dry in the past together in vacuum oven, in the sub-dry air of dry product, under 700 ℃ of temperature, activation (calcination) 3 hours obtains catalyzer L of the present invention.

Second example is mixed the whole catalyst components that use among the catalyzer L of the present invention in the presence of methyl alcohol, drying, calcination in vacuum oven as mentioned above, obtain catalyzer M of the present invention.

Every kind of catalyzer calculates when pressing drying, and (calcination) contains 4% silicon-dioxide approximately, and chromium and fluorine are about 2.1% respectively, and all the other are aluminum oxide.

Every kind of catalyzer is got portion to be mixed with another kind of custom catalysts, this catalyzer is to be loaded with 1%(weight at aluminum phosphate) sexavalent chrome, the P/AL atomic ratio is 0.9, and in dry air, under 700 ℃ of temperature with this catalyst activation 3 hours, this catalyzer is called 0 for simplicity.

With ethene with in some experimental examples, ethene is mixed with the 1-hexene and carries out successive polymerization in the ring reaction device of 23 gallons (87 liters), and temperature in accordance with regulations is a thinner with Trimethylmethane also.Triethyl-boron is a promotor, and the hydrogen of necessary amount is auxiliary.In this process, catalyzer adds off and on liquid slurry form in normal hexane, and it adds speed and is enough to keep needed polymer output.By sedimentation pipe (Settling leg), liquid being starched product cycle from reactor of form shifts out, flash off thinner and volatile gases and product is stored, " loose matter " that obtain stablizes it with general multi-component system, add total amount and reach 0.2%(weight) stablizer, 2.6-two-Te-butyl-4-methylphenol for example, dilauryl thiodipropionate, Zinc Stearate, then, estimate its various physical propertiess.

Catalyst system, reaction conditions and gained result are shown in table VI and table VI A.

Table VI vinyl polymerization, single catalyst, no hydrogen

The experiment number	Catalyzer number	TEB ppm	Calculating productive rate gram/gram catalyzer/hour	Temperature of reactor, ℃	Polymkeric substance
									The density grams per milliliter		The limiting viscosity deciliter/gram	The melt viscosity megapoise
					(a) loose matter		Mold pressing
									1	L	1	1330	93	0.474	0.9402	16	（b) －
2	L	2	1590	93	0.468	0.9401	15	－
									3	M	3	2500	93	0.450	0.9412	14	34
4	M	1	1320	83	0.474	0.9414	-	49
									5	M	4	1650	82	0.482	0.9402	16.5	52
6	M	4	1740	82	0.461	0.9403	Insoluble	53
									7	M	4	1920	87	0.471	0.9400	Insoluble	54
8	M	4	2040	88	0.460	0.9408	Insoluble	47
									9	M	4	1450	88	0.455	0.9398	11.6	29

(a) tap density

(b) dash is represented not measure.

The result shows shown in the table VI, in the experiment 1～3, temperature of reactor is constant, increases along with the content of TEB increases productive rate, tap density reduces, it is basic identical that mold pressing density keeps, and according to the limiting viscosity data, polymericular weight reduces, although limiting viscosity result is less than 20, but the melt viscosity result shows and is all making ultrahigh molecular weight polyethylene(UHMWPE) in the experiment that therefore, all experiments all are considered to experiment of the present invention.The molecular weight of just testing 6 to 8 resulting polymers is too high can not to be dissolved.At TEB content is under the constant situation of 4ppm, and the result of experiment 5 to 8 shows that along with temperature of reactor rises, productive rate also increases, and the tap density of polymkeric substance reduces, and just mold pressing density slightly changes, and resulting yield results is enough to have commercial significance.

Table VI A lists the result who uses the catalyst mixture that catalyzer of the present invention is arranged to prepare Alathon and ethene-1-hexene copolymer.The homopolymer that these bifurcation homopolymer of preparation show to list in the V in flow process 10 to 13 has higher density.This has reflected and has contained ALPO ₄The influence of catalyzer.In these experiments, along with TEB content increases, productive rate also increases like before.The scope of the HLMI value of all polymer beads (granular loose matter) approximately from 7 to 43; also show the significant ESCR that shows high rigidity, this shows at least by partial polymer wherein, for example; HLMI is about 20 or less than 20 polymkeric substance, just can produce good film.As expectation, the modulus in flexure of polymer samples also reduces with density and lowers.

Example 7

Phosphorylation, silication is fluoridized, aluminum oxide-sexavalent chrome catalyzer and vinyl polymerization

With containing 85%H ₃PO ₄Methanol solution dipping be suspended in high pore volume aluminum oxide in the methyl alcohol, to prepare a series of catalyzer, used H ₃PO ₄Amount will make the phosphorus amount that contains the calculating that reaches required on the catalyzer.In addition, in these catalyzer of the present invention, also add the NH in the methyl alcohol of being dissolved in of q.s ₄HF ₂, Silbond ₄₀, and Cr(NO ₃) ₃9H ₂O is so that in the dry constituent that makes, contain the chemically combined fluorine that reaches required calculating, SiO ₂And chromium.Every kind of mixture is in vacuum oven, and is dry under 80 ℃ of temperature; Then under 700 ℃, in the dry air, activation (calcining) 3 hours, the change time then indicates in addition.

Then, it is described as example 2 that every kind of catalyzer that activated is got portion, checks in vinyl polymerization, uses 8ppmTEB as promotor.

Used condition and obtain the results are shown in the table VII.

(a) control experiment is as table III experiment 8

(b) inapplicable, or undetermined

(c) relatively, with table V experiment 6, i.e. the present invention tests but does not have phosphoric acid salt

(d) relatively, with table V experiment 8, i.e. the present invention experiment, but do not have phosphoric acid salt

(e) with the carrier of original technology, compare usefulness

(f) as preceding table as stating, proofread and correct to 30 minute reaction times, parenthetic calculating is the productive rate of actual experiment time

(g) in the experiment 5.0 milliliters of 1-hexenes and 50 pounds/inch are arranged ²Hydrogen

(h) in the experiment 50 pounds/inch is arranged ²Hydrogen

Result in the observation table VII can find out, by handling carrier with one or more aforementioned chemical reagent, be stated from sexavalent chrome catalyzer on the aluminum oxide can regulate produce needed high-load melting index scope-from zero to be about 4 or higher-polymkeric substance.Without chemical treatment, can find out Cr from control experiment 1 ^{+ 6}Being stated from the aluminum oxide is SA ethylene rolymerization catalyst.Comparative experiments 2 and 3 shows Cr ^{+ 6}Be stated from fluoridize, be active catalyst on the aluminium oxide silicide, can produce ultrahigh molecular weight polyethylene(UHMWPE), equal 0 as HLMI.Comparative experiments 4 and 5 shows Cr ^{+ 6}Be stated from the phosphorylation aluminum oxide and draw active catalyst, can produce low-molecular weight polymer, be about 1, rather than test the UHMWPE in 2 and 3 as HLMI.Remaining the present invention tests 6 to 15 and shows, when not having hydrogen, and Cr ^{+ 6}Be stated from phosphorylation, fluoridize, the comparison of the catalyzer on the aluminium oxide silicide has more activity according to catalyzer, test 11 as the present invention, its productive rate is about per 30 minutes every gram catalyzer 3500 gram polymkeric substance, and the HLMI value of this polymkeric substance generally occupy with the polymkeric substance (example of fluoridizing, aluminium oxide silicide prepares, HLMI is 0) with only between the polymkeric substance (example, HLMI is about 1) with the preparation of phosphorylation aluminum oxide.

When in reactor with hydrogen as molecular weight regulator, then prepare the polymkeric substance of low HLMI value, for example, the present invention tests 9,12,15, the scope of its HLMI value approximately from 1.5 to 3.5.

Therefore, with regard to productive rate, although be equal to or be better than some contrast invention experiments with the experiment 5 of original technology, and phosphorylation catalyzer of the present invention has greater flexibility for the control of molecular weight, and the comprehensive best result who obtains, as tests 11.

Example 8

Aluminum oxide-aluminium phosphate catalyst (porose cogelled)

Prepare a series of catalyzer by aforesaid macropore volume aluminum oxide with contact process, the same with aforementioned example, add fluoram, silicon-dioxide and ortho-phosphoric acid (when need add fashionable) are also used the AIPO of preparation usually ₄Slurry carries out modification and handles and make.By with ALPO ₄Gelling realizes contact in the hole of the aluminum oxide of modification, for example, prepare a kind of AL(NO that contains aequum ₃) ₃9H ₂O, NH ₄H ₂PO ₄And Cr(NO ₃) ₃9H ₂The strong solution that O is water-soluble.Then, it is joined in the aluminum oxide of modification, absorb hand-hole, obtain looking like dried powder with the blended mode.The slurries amount must be equal to or less than the pore volume of modified aluminas, and then adds ammonium hydroxide, makes slurries form gel in the hole of catalyzer that with the aluminum oxide is carrier.Also can add sal volatile makes the slurries gelling form ALPO ₄Gel.The mixture (or porose cogelled) that generates washes with water, again with the alcohol washing, and filtering separation, then that product is dry in vacuum oven, and in dry air, calcining and activating is to be used for polyreaction under the high temperature.Adopt another kind of program, then will contain ALPO ₄The slurries of gel spray on the aluminum oxide of modification.

In all examples, this mixed catalyst through separate and drying after, be with in the past the same in dry air, 700 ℃ of temperature lower calcinations 3 hours cool off then, storage is got up in nitrogen.

Listed modified aluminas in the table VIII, the calcining temperature that adopts after the modification is used ALPO ₄The time AL that calculates and the atomic ratio of P, the modified aluminium oxide supports of calculating and ALPO ₄The weight ratio of carrier (based on dry measure), and total chromium amount (based on dry measure) in the hybrid catalyst system that calculates.

Example 9

The mixed catalyst polymerising ethylene of use-case 8

According to the mode that example 4 adopts, to get each portion of every kind of catalyzer and carry out vinyl polymerization, temperature is 96 ℃, adding 8.3ppm TEB is promotor, 50 pounds/inch ²Hydrogen is conditioning agent, and other situation then has appointment in addition.

It the results are shown in the table IX

With these difunctional " porose cogelled " catalyst complex, can obtain high molecular and low-molecular-weight tight dimorphism mixture, and needn't spend again the polymkeric substance fusion later on.Such polymkeric substance all is useful in made membrane and blow molding.

(a),, productive rate is proofreaied and correct productive rate when being 30 minutes then as described in the preceding table if the reaction times is not 30 minutes.

(b) dash is represented not measure

(c) polymerization temperature adopts 100 ℃, but reactor general pressure with all other experiment equally adopt 565 pounds per square inch absolute (psia) (pound/inch ²), this means, if thinner has higher dividing potential drop, then require the dividing potential drop of ethene smaller, to guarantee 565(pound/inch ²) pounds per square inch absolute (psia).

ESCR COND.A: the stress cracking of anti-atmosphere the, condition A.

The result that table obtains in the IX shows, with mixing, or " porose cogelled " catalyzer can prepare the high-density homopolymer, and shown in the HLMI value, can obtain the molecular weight of relative relative broad range.In this series catalyst, along with ALPO ₄The minimizing of catalyst based amount, density polymer increases, and with testing the high yield result who obtains in 1 and testing the low-yield result who obtains in 2 and compare, can find out the restraining effect of hydrogen to productive rate.In the presence of hydrogen, as noticing among the 2P to 6P, obtain the polymkeric substance of lower molecular weight in experiment, wherein, the scope of gained HLMI value approximately from 3 to 63, and in testing 1P, this is worth less than 0.1.All samples all has extraordinary ESCR and inflexible combination.

Example 10

In order to illustrate, prepare catalyst series with silica supports with containing sexavalent chrome catalyzer on the aluminum oxide that is stated from processing and the ethene polymers that contains sexavalent chrome Preparation of Catalyst on the silicon-dioxide that is stated from similar processing and the silica-alumina in qualitative difference.

Used silicon-dioxide is 952 grades of Davison, has about 300 meters ²The surface-area of/gram, pore volume, the silica-alumina of about 1.6 milliliters/gram are Davison MS13-11D levels, are 87% silicon-dioxide and 13%AL by weight ₂O ₃Form.Its surface-area is about 300 meters ²/ gram, pore volume are about 1.1 milliliters/gram.Every kind of carrier is all used the Cr(NO of q.s ₃) ₃Aqueous solution dipping is made calculated weight and is 1% chromium, forms with chromic oxide to exist, and be benchmark with composition last, that activated during calculating.

In addition, every kind of silica supports is the same with former alumina supporter, by the NH of aforementioned the same manner with q.s ₄F ₂, Silbond

40 and Cr(NO ₃) ₃Handle, get to the end, the composition that activated, every kind of composition contains the chromium that 1% calculated weight exists with the chromic oxide form, 2% F, the SiO of 3.7% interpolation ₂

Every kind of catalyzer is used for the vinyl polymerization that carries out at batch reactor, and total reactor pressure is 656 pounds per square inch absolute (psia) (pound/inch ²), containing 8ppm TEB, polymerization methods is as previously mentioned.

The activation temperature of catalyzer and obtain the results are shown in the table X among.

The table X is that the catalyzer of carrier carries out vinyl polymerization in order to silicon-dioxide

The experiment number	Catalyzer		Temperature of reactor ℃	Reaction times minute	Calculated productive rate (a) gram/25 minutes	Polymkeric substance HLMI
							Carrier	Temperature ℃
	1	S?i?O ?2							750	90	20	3040	0.67
2			S?i?O ?2	650	95	22	2670	1.8
	3	S?i?O ?2							650	(b) 90	25	2030	2.1
4			F-S?i?O ?2/S?i?O ?2	700	90	22	0	-
	5	S?i?O ?2-A?L 2?O 3							700	(c) 85	25	835	2.7
6			F-S?i?O ?2/S?i?O ?2-A?L 2?O 3	700	(c) 85	25	227	0.28

(a),, will calculate productive rate and be corrected to 25 minutes by former described mode if the reaction times is not 25 minutes.

(b) experiment is having 50 pounds/inch ²Hydrogen under carry out

(c) experiment is having 50 pounds/inch ²Hydrogen and 5.0 milliliters of 1-hexenes under carry out.

Experiment 1 shows in 3,5,6 result, is the HLMI of the polymkeric substance that can survey of the catalyzer gained of carrier in order to silicon-dioxide, and being different from is the ultrahigh molecular weight polyethylene(UHMWPE) of the Preparation of Catalyst of carrier with the aluminum oxide with similar processing.

In addition, with fluoridize, siliconizing be that the catalyzer of carrier causes catalyst performance to reduce with silicon-dioxide, this is different from, and the usefulness shown in the table V is fluoridized, siliconizing be the performance of the catalyzer of carrier with the aluminum oxide.

Example 11

Close the combination of chromium with Chromocene and diisopropylbenzene(DIPB) and carry out vinyl polymerization

Closing chromium (0 valency) and Chromocene(2 valency with diisopropylbenzene(DIPB)) chromium dipping fluoridizes and aluminium oxide silicide, and polymerization process is controlled molecular weight with hydrogen, obtains following result.

The table XI

The experiment number	Carrier	Chromium	(4) density	（5） Flex	Melting index (MI)	(6) limiting viscosity
							1	ALPO 4	Chromocene	0.9513	1228	0.51	-
2	ALPO 4	(1) D?c?c	0.9538	963	0.14	-
							3	ALPO 4	(3) Chromocene+Dcc	0.9500	1064	0.26	-
4	ALPO 4	″	0.9485	888	0.24	-
							5	(2) AL 2?O 3	″	0.9582	1542	0.21	-
6	″	″	0.9648	1592	2.7	-
							7	(2) AL 2?O 3	(3) Chromoc ne+Dcc	0.9286	-	-	19
8	″	″	0.9276	-	-	20

(1) diisopropylbenzene(DIPB) closes chromium

(2) handled with fluorizating agent and silication agent

(3) 1: 1 mole ratio

（4）ASTM D-1505

(5) modulus in flexure, ASTM D-790, megabar

(6) see Table II, annotate (b)

Experiment 7 and 8 shows that the aluminum oxide that has the processing that mixes 0 valency and divalent chromium of the present invention can obtain having very highdensity extra high molecular polymer.Experiment 5 and 6 shows to have and mixes 0 valency and chromous aluminum oxide of the present invention (and H ₂Make and obtain low-molecular weight polymer) very high density and rigidity can be provided, than in order to ALPO ₄The result who obtains for carrier is good, and it is 3 and 4 good promptly to test.

Example 12

The data that propose below are to use Cr(6+ for illustrating)/F-AL ₂O ₃Catalyst system can be prepared the polymkeric substance with uncommon characteristic.As what announce at this body matter, this catalyzer can be produced the polyethylene of ultra-high molecular weight, UHMWPE.In general, for such polymkeric substance in the technology that had in the past, density reduces with molecular weight.The special character of above mentioned sexavalent chrome system is, the ultrahigh molecular weight polyethylene(UHMWPE) polymkeric substance of being produced has up to the present to the polymkeric substance of similar molecular weight the highest viewed density, according to the ASTM method, D-4020-81, D-2857-70 and D-1601-78, molecular weight usually are associated with the viscosity of the naphthalane solution of standard.The method of the determining molecular weight that another kind is of little use is the melt viscosity that the rheology spectrum is surveyed polymkeric substance, and service temperature is 230 ℃, and p.s., vibrational frequency was 1 radian.Data sheet among Fig. 1 and Fig. 2 is understood above-mentioned relation.By the measured value of molecular weight, promptly melt viscosity and limiting viscosity show Cr(6+)/F-AL ₂O ₃The polymkeric substance that catalyzer is produced, within a similar molecular weight ranges, its density is with the resulting density height of a lot of comparative catalyst.

What make is characteristic new polymers, and its melt viscosity (megapoise) is 35 or bigger, and unique is 40～60, is 50 or bigger in some cases; Its density is 0.940 grams per milliliter or bigger, and what have more characteristic is about 0.940～0.950, preferably greater than 0.945 grams per milliliter.According to characteristic, viscosity, the new polymers that is provided has the limiting viscosity greater than 13 Grams Per Minute rice, what have more characteristic is 13～17, or be 15 to 20 in some cases, its density is greater than 0.940 grams per milliliter simultaneously, what have more characteristic is 0.940～0.950, and preferably its density is greater than 0.941 grams per milliliter.

Example 13

Buy chromium chloride (II) and Grignard reagent from alpha (ALfa) chemical company, the trimethyl silicane methylmagnesium-chloride, the whole solvents that use are SILVER REAGENT, and by suitable siccative (normally calcium oxide) distillation.Before the use, in argon gas, preserve.Except as otherwise noted, all operation is all carried out in argon gas or nitrogen rare gas element.

Eight (μ-trimethyl silane methyl) four chromium (II) (Cr ₄(Tms) ₈) synthetic.

With 5 gram CrCl ₂(40.7 millimole) exists low suspension in 100 milliliters of THF at argon gas.Cool off this suspension to-30 ℃, under agitation slowly add the Ge Liya solution-ClmgCH of 50 milliliters of THF dilutions of 50 milliliters of usefulness ₂Si(CH ₃) ₃(1.67 mol are in ether).After all adding, make reaction soln be warming to room temperature, and at room temperature stirred 1 hour, remove volatile matter then under vacuum, residuum respectively extracts with 100 milliliters of pentanes for three times.The extraction liquid of collecting is filtered by glass wool, and the cumulative volume of solution is reduced to 50 milliliters.After under-78 ℃ of temperature, placing 24 hours, from mother liquor, isolate the microcrystal of brownish black, use cold (78 ℃) pentane once washing again, then, at-78 ℃, vacuum (10 ^-4Torr) drying is 20 hours under, output: 5.18 gram products (5.73 millimoles, 56%), Cr ₄(TMS) ₈By being evaporated to drying, from mother liquor, can also reclaim 1.20 gram products.Ultimate production is: 6.38 grams (7.05 millimoles, 69%).Analyze: for Cr ₄(TMS) ₈, C ₈₂H ₈₈Si ₈Cr ₄, molecular weight=905.728

C ^a）H ^a）Cr ^b）

Calculate: 42.44 9.79 22.96

Find: 42.28 9.89 25.34

A) by C, H, N, ultimate analysis

B) by the plasma X-ray analysis X

Draw as follows by the structural formula that the monocrystalline X-ray diffraction is measured:

R＝CH ₂SiMe ₃

Example 14

Will be identical with example 1 catalyzer D fluoridize, aluminium oxide silicide carrier calcining, use four (trimethyl silane methyl) chromium (1 V) solution impregnation then, obtain containing the chromium of 1% weight level, polymeric reaction temperature is 95 ℃, reactor pressure is 550(pound/inch ²) gauge pressure, productive rate is very high.

Its result is as follows;

（a）ASTmD-1505

（b）ASTmD-790

For purposes of illustration, the present invention has been done detailed description, but this present invention be can not be interpreted as and just limit to these, but all changes and improvement within the spirit and scope of the invention tried hard to be included in.

Used symbol is defined as follows among Fig. 1:

●: Cr(6+)/the F-Al203 catalyst

□：TiCl ₄/SiO ₂-TEA

△: tetrabenzyl zirconium

○：VC12/P-Al203-TEA

◆: two (cyclopentadienyl) chromium II (CHROMOCENE)/AlPO ₄

◇: two (cyclopentadienyl) chromium II (CHROMOCENE)+Cr(2+)/AlPO ₄

+: two (cyclopentadienyl) chromium II (CHROMOCENE)/F-Al203

*: the industrial polyvinyl resin with super-high molecular weight of Hirst (HOECHST) company, GUR413.

Used symbol is defined as follows among Fig. 2:

●: Cr(6+)/the F-Al203 catalyzer

□：TiCl ₄/SiO ₂-TEA

○：VC12/P-Al203-TEA

△: two (cyclopentadienyl) chromium II (CHROMOCENE) AlPO ₄

◆: two (cyclopentadienyl) chromium II (CHROMOCENE)+Cr(2+)/AlPO ₄

+: two (cyclopentadienyl) chromium II (CHROMOCENE)/F-Al203

*: the industrial polyvinyl resin with super-high molecular weight of Hirst (HOECHST) company, GUR413.

Claims (10)

1, the application of catalyzer in olefinic polymerization, it is included at least a under the polymerizing condition-1-alkene and contacts with a kind of promotor with catalyzer, described Preparation of catalysts comprises uses silication agent steam to contact with described aluminum oxide, at described alumina surface the silication agent is transformed into silicon-dioxide then, the consumption that described silication is stated should be enough to the silicon-dioxide (in the weight of aluminum oxide) of to 0.5 to 10% (weight), the consumption that described aluminum oxide also stands fluorizating agent should make the fluorine that obtains 0.5 to 3% (weight) on described aluminum oxide, then be incorporated into the chromium component on the described carrier and generate described catalyzer, at last with described catalyzer and the promotor combination that is selected from organoboron compound and organo-aluminium compound.

2, application according to claim 1, wherein said silication agent is a polysiloxane, this polymer siloxane changes into silicon-dioxide by the temperature lower calcination in 500 ℃ to 800 ℃ in air at described alumina surface after described processing.

3, application according to claim 1, wherein said aluminum oxide with handle with described fluorizating agent before described silication agent contacts.

4, application according to claim 3, wherein said fluorizating agent is an ammonium bifluoride.

5, application according to claim 1, described Preparation of Catalyst also comprise carries out phosphorylation or phosphitylation processing to described aluminum oxide.

6, method according to claim 5, wherein said aluminum oxide is calcined in air under 300 to 700 ℃ temperature, then with contact with the methanol solution of phosphoric acid before described silication agent contacts.

7, application according to claim 1, described Preparation of Catalyst also are included in the well-oxygenated environment and under 500 ℃-800 ℃ temperature the composition that obtains are activated, so that at least a portion chromium in the described chromium component becomes 6 valence states.

8, application according to claim 7, wherein said chromium component is selected from chromium trioxide, chromium acetate and chromium nitrate, the consumption of described chromium component will reach 0.1 to 5%(weight enough) chromium (in the weight of aluminum oxide), wherein said well-oxygenated environment is an air.

9, application according to claim 1, wherein the chromium component is that Yang Ge is arranged, described aluminum oxide is activated under 150 to 1000 ℃ temperature before introducing described chromium component.

10, application according to claim 9, wherein said organo-chromium compound is selected from: eight-(μ-trimethyl silane methyl) four chromium (II), four-(trimethyl silane methyl) chromium (IV), two-(cyclopentadienyl) chromium and diisopropylbenzene(DIPB) close chromium.

Images