Abstract: In a process for the oligomerization of alpha olefins using a boron trifluoride/alcohol catalyst complex a method for recovering the boron trifluoride from the product stream which comprises lowering the pressure of the product stream to flash off excess boron trifluoride, mixing the boron trifluoride with fresh alcohol to form fresh boron trifluoride/alcohol catalyst complex, and introducing the fresh catalyst back into the oligomerization reactor.

Abstract: The present invention is a two-component catalyst system comprising (a) an alkyl magnesium (MgR2) component and (b) a Lewis acid component. The catalyst system is used for catalyzing the oligomerization and polymerization of ethylene and/or &agr;-olefins to form homopolymers and copolymers. The products range from highly linear, high molecular weight, solid polymers to highly branched, lower molecular weight oils.

Abstract: A catalyst and a process are provided for oligomerizing ethylene. A heterogeneous catalyst system comprises: (1) a chelating ligand, preferably 2-diphenyl phosphino benzoic acid (DPPBA); (2) a nickel precursor, preferably nickel chloride hexahydrate (NiCl2.6H2O); (3) a catalyst activator, preferably sodium tetraphenylborate (NaBPh4); and (4) silica. A 1:1:1 molar ratio of Ni:DPPBA:BPh4 catalyst components are fixed on a silica support using low-temperature fixation. The catalyst components are dispersed in a diluent, preferably ethanol, and silica is added. The ethanol is evaporated using freeze-drying equipment to form a silica-supported catalyst system. The silica-supported catalyst is slurried in ethanol in a reactor, and ethylene is added. The reactor pressure and temperature are maintained at about 725 psig and 100° C., respectively, for about two hours.

Abstract: A process for oligomerizing an acyclic monoolefin monomer in which the oligomerization is controlled to produce predetermined relative amounts of at least two preselected oligomers in a higher boiling fraction of the oligomerization products and the lower boiling products are recycled to the oligomerization reaction.

Abstract: The present invention relates to at least simply unsaturated polyolefins with a number mean molecular weight in the range of 400 to 1,500 dalton and a dispersibility of M.sub.W /M.sub.N <1.2, obtained through catalytic dimerization from at least simply unsaturated olefin-oligomers, as well as to the method for their production. The present invention further relates to derivatives of these polyolefins which can be obtained by functionalizing at least a double link of the polyolefin. The invention also relates to the use of polyolefins and/or functionalization products as additives for fuels or lubricants.

Abstract: The present invention provides a novel catalyst system which can be preferably used in the trimerization, oligomerization reaction or polymerization reaction of an olefin, and a method for the trimerization, oligomerization or polymerization reaction of an olefin, which comprises using the catalyst system. A catalyst system obtained by contacting the following components (A) to (C):(A) a chromium compound,(B) an imine compound, and(C) a metal alkyl compound, and a method for the trimerization, oligomerization or polymerization reaction of an olefin, which comprises using the catalyst system are disclosed.

Abstract: Disclosed are hot-melt adhesive compositions suitable for the manufacture of soft goods. They have a melt viscosity of 60,000 mPa.s or less at a temperature of 120.degree. C. and include: (a) 50 to 150 parts by weight of a styrenic block copolymer or mixtures and/or modified and/or hydrogenated derivatives thereof; (b) 20 to 450 parts by weight of a tackifying resin which, when incorporated into a reference composition, leads to the following properties:a tan .delta. value of 3.5 or less, wherein tan .delta. is defined as the ratio between the loss modulus and the storage modulus of said composition andan elastic retention on spandex fibers (300%) or natural latex rubber (200%) after 4 h at 40.degree. C. of 70% or more; anda crossover temperature of 95.degree. C. or less.Further disclosed are novel partially hydrogenated hydrocarbon resins which are useful as tackifying resins and have the following properties: (a) a R&B softening point (R&B) of 50.degree. C. to 150.degree. C.

Abstract: A boron trifluoride complex can be recovered without changing its molar coordination ratio, by applying a direct and/or alternating voltage to an electrically-nonconductive fluid in which at least a part of boron trifluoride complex is dispersed and/or dissolved, and separating the boron trifluoride complex by settling from the electrically-nonconductive fluid. By utilizing this method for the preparation of olefin oligomer using a boron trifluoride complex catalyst, it is possible to reuse the recovered catalyst as it stands for the reaction.

Abstract: This invention concerns a process for recovering BF.sub.3 from a BF.sub.3 /promoter complex catalyzed .alpha.-olefin oligomerization product stream, which process comprises thermally cracking the complex in the product stream to yield BF.sub.3 gas, and contacting the BF.sub.3 gas with a cold .alpha.-olefin stream containing a promoter.

Abstract: Catalysts and processes are described to make low molecular weight, essentially terminally-unsaturated, viscous poly(1-olefin) or copoly(1-olefin) having a high terminal vinylidine content from a feed stock containing one or more 1-olefin and other volatile hydrocarbon liquids using a Ziegler catalyst made from a Group IVb metallocene and an aluminoxane cocatalyst, particularly bis(cyclopentadienyl) and bis(indenyl) titanium(IV), zirconium(IV) or hafnium(IV) compounds and methylaluminoxane. A particularly useful feed stock is a refinery stream containing 1-olefins and isobutylene which is used to make polyisobutylene.

Abstract: A process is described for the production of hydrocarbons with a high octane number starting from hydrocarbon cuts containing isobutene by selective dimerization with acid catalysts characterized in that the dimerization reaction is carried out in the presence of primary alcohols and alkyl others in such a quantity as to have in the feeding a molar ratio primary alcohols+alkyl ethers/isobutene of more than 0.1 and a molar ratio primary alcohols/isobutene of less than 0.2, operating, preferably, at a reaction temperature of between 30 and 120.degree. C., at a pressure of less than 5 MPa and feeding space velocities of less than 30 h.sup.-1.

Abstract: A monoolefin oligomerization process which gives high yields of diner and trimer at high monoolefin conversions in a single stage reaction is described. The process involves contacting a C.sub.6-20 oligomerizable olefin with a catalyst comprising boron trifluoride and from 0.05 to 2.5 mol %, based on the total quantity of monoolefin being used, of an alcohol catalyst promoter which is added portionwise during the oligomerization. The oligomerization is performed at a temperature of 45-90.degree. C. and under a pressurized atmosphere of boron trifluoride until the monoolefin conversion is at least 90% and the combined total of dimer and trimer in the liquid reaction mixture is at least 70% by weight.

Abstract: A synthetic lubricant material is produced by forming a catalyst complex of a boron trifluoride catalyst and at least one alcohol promoter in the absence of olefinic monomer, then oligomerizing a C.sub.4-16 olefinic monomer by adding the olefinic monomer to a reaction vessel containing the catalyst complex, under boron trifluoride pressure, to produce an oligomer product. At least 50 weight % of the olefinic monomer is C.sub.8-16 olefinic monomer.

Abstract: A process for controlling the molecular weight distribution of polyisobutene formed during a liquid phase polymersiation reaction using a catalyst comprising boron trifluoride and taking place in a reactor having condensers associated with it which process involves introducing an electron donor above the level of liquid in the reactor to minimize the reaction of isobutene with free gaseous boron trifluoride in the condensers thereby minimizing the formation of unwanted polymers.

Abstract: Low molecular weight, highly reactive polyisobutene having an average molecular weight M.sub.n of from 500 to 20000 Dalton and containing over 80 mol % of terminal double bonds is prepared by the polymerization of isobutene or an isobutene-containing hydrocarbon stream in the liquid phase and with the aid of a boron trifluoride complex catalyst at from -40 to 0.degree. C. and at from 1 to 20 bar, by a process in which the polymerization reaction is carried out in at least two polymerization stages, the added isobutene being polymerized to a partial conversion of up to 95% in the first polymerization stage and the polymerization of the remaining isobutene being continued in one or more subsequent polymerization stages, without or after prior isolation of the polyisobutene formed in the first polymerization stage.

Abstract: Alpha-olefin oligomers are produced by oligomering alpha-olefin monomer with a catalyst system comprising boron trifluoride, a protic promoter, and a special type of modifier. The modifier is a compound that satisfies the following criteria: (a) it has at least one moiety in which a carbonyl group is directly bonded to a nitrogen atom which is in turn bonded to two separate carbon atoms, (b) it is devoid of any nitrogen atom other than a nitrogen atom that is either (i) directly bonded to two separate carbon atoms and to a carbonyl group or (ii) is triply bonded to a single carbon atom, and (c) it is devoid of any protonic functional substituent. These modifiers control the oligomer product distribution and provide higher percentages of lower oligomers, especially dimers.

Abstract: Polyisobutene having an average molecular weight M.sub.n of from above 5000 to 80,000 dalton and containing more than 50 mol % of terminal double bonds is prepared by a novel process, by cationic polymerization of an isobutene-containing hydrocarbon mixture in. the liquid phase in the presence of a boron trifluoride complex catalyst, and has a dispersity of M.sub.w /M.sub.n of from 2 to 4 and is contained in lubricants.

Abstract: A monoolefin oligomerization process which gives high yields of dimer and trimer at high monoolefin conversions in a single stage reaction is described. The process involves contacting a C.sub.6-20 vinyl olefin with a catalyst comprising boron trifluoride and from 0.075 to 0.5 mol %, based on the total quantity of monoolefin being used, of an alcohol catalyst promoter. The oligomerization is performed at a temperature below about 40.degree. C. and under a pressurized atmosphere of boron trifluoride in the range of 2 to 4 bars gauge until the monoolefin conversion is at least 95% and the combined total of dimer and trimer in the liquid reaction mixture is at least 60% by weight.

Abstract: A process is provided to trimerize or oligomerize olefins in the presence of an olefin oligomerization catalyst and a solvent which is a product of the olefin oligomerization process.

Abstract: BF.sub.3 is vaporized from specified crude polyolefin reaction product mixture in a vaporization zone at a temperature insufficient to decompose BF.sub.3 or any BF.sub.3 promoter complex in the mixture, and the vaporized BF.sub.3 may be recovered directly. Further, a process for the oligomerization of a liquid olefin composition and recovery of BF.sub.3 is described in which inert volatile material present in a liquid olefin composition is removed from the composition by vaporization, forming a degassed liquid olefin composition free of inert volatile material. The degassed liquid olefin composition is then contacted in a reaction zone with BF.sub.3 under conditions to oligomerize the olefin, forming crude polyolefin oligomerization reaction product mixture containing dissolved BF.sub.3, which may be treated as described.

Abstract: A method for removing catalyst from an olefinic oligomerization product includes the steps of oligomerizing one or more olefins in the presence of a BF.sub.3 cocatalyst complex, and distilling the oligomerization product while separating vaporized BF.sub.3 cocatalyst complex, the distillation step including, simultaneously to the separation of BF.sub.3 cocatalyst complex, a separation of vaporized unreacted monomer from a bottom product which becomes substantially free from BF.sub.3 cocatalyst complex.

Abstract: Alpha-olefin oligomers are produced by oligomerizing an alpha-olefin monomer with a catalyst system comprising boron trifluoride, a protic promoter, and a modifier which is (a) at least one 1,3-dioxolane, or (b) at least one 1,3-dioxane, or (c) a combination of (a) and (b). Use of these modifiers in the BF.sub.3 -catalyzed oligomerization makes it possible to modify the promoted catalytic reaction so that product containing as much as 50% or more of dimer can be produced at high conversions, at modest reaction temperatures, and in short reaction periods.

Abstract: An oligomerization catalyst according to the invention comprises a nickel compound (A); an organophosphoric compound (B); an organoaluminum compound (C); and a compound of the group consisting of carbon-halogen bond-containing compounds, oxoacid and salts thereof, sulfonic acid and derivatives thereof, and compounds of any of the formulae QX.sup.4.sub.n, QR.sub.n, QR'.sub.n, QX.sup.4.sub.1 R.sub.m, QX.sup.4.sub.1 R'.sub.m, QR.sub.1 R'.sub.m, Q.sup.1 (BR.sub.4).sub.p and R"(BR.sub.4) wherein Q is an element of the group consisting of Mg, Ti, Zr, B and Sn, Q.sup.1 is an element of the group consisting of Li, Na, K, Ca and Zn, X.sup.4 is a halogen or hydrogen atom, R is a C.sub.1 -C.sub.12 hydrocarbon group, R' is a C.sub.1 -C.sub.12 oxygen-containing hydrocarbon group, R" is a C.sub.1 -C.sub.20 hydrocarbon group or an ammonium group, n is a valence of Q, l, m is a natural member that satisfied n=l+m, and p is a valence of Q.sup.1. This catalyst is useful for the production of alpha-olefinic oligomers.

Abstract: A process for the recovery of BF.sub.3 from crude oligomerization reaction product mixture containing dissolved BF.sub.3 is described, the process being characterized by vaporization of BF.sub.3 from the crude oligomerization reaction product mixture in a vaporization zone at a temperature insufficient to decompose BF.sub.3 or any BF.sub.3 promoter-complex in the mixture. BF.sub.3 from the vaporization zone is then contacted with a liquid olefin composition under conditions to absorb BF.sub.3, in an absorption zone, forming a mixture comprising liquid olefin composition and BF.sub.3. The liquid olefin composition may be utilized directly for oligomerization of the liquid olefin therein.

Abstract: Alpha-olefin oligomer is prepared by contacting an alpha-olefin monomer which contains from about 6 to about 20 carbon atoms with a catalyst system comprising boron trifluoride, a protic promoter, and an organic sulfone, sulfoxide, carbonate, thiocarbonate, or sulfonate. Oligomer containing as much as 50% or more of dimer can be produced at high conversions, at modest reaction temperatures, and in acceptably short reaction periods.

Abstract: A supported catalyst component for an olefin polymerization catalyst comprising a solid particulate support, a magnesium halide, and optionally a Group 4 or 5 transition metal compound, a Group 2 or 13 organometal compound, and an electron donor, wherein a majority of particles of the solid particulate support is in the form of an agglomerate of subparticles. A process for preparing this supported catalyst component. A catalyst composition comprising this catalyst component and a cocatalyst. An olefin polymerization process using such a catalyst composition.

Abstract: Alpha-olefin oligomers are prepared by a process which comprises contacting an oligomerizable olefin monomer with a catalyst system comprising a catalytic amount of boron trifluoride, a protic promoter, and an organic modifier selected from the group consisting of phosphate, thiophosphate, phosphine oxide, and phosphine sulfide. The oligomerizable olefin monomer is a C.sub.6 to C.sub.20 linear olefin comprising at least 50 mole % alpha olefin.

Abstract: Immobilized Lewis Acid catalyst comprising polymer having at least one Lewis Acid immobilized within the structure therein, said polymer having monomer units represented by the structural formula:--[A].sub.a --[B].sub.b --[C].sub.c --wherein a represents about 1 to about 99 mole %b represents about 0 to about 50 mole %c represents about 1 to about 99 mole %a+b+c is preferably about 100%; ##STR1## C is selected from the group consisting of: ##STR2## (III) combinations thereof, wherein D is OH, halide, OR.sup.4, NH.sub.2, NHR.sup.3, OM', or OM";E is the residue of the reaction of at least one Lewis Acid with the D substituent of monomer unit B;R.sup.1 represents proton, C.sub.1 -C.sub.24 alkyl group, or C.sub.3 -C.sub.24 cycloalkyl;R.sup.2 represents C.sub.1 -C.sub.24 alkylene group, C.sub.3 -C.sub.24 cycloalkylene, C.sub.6 -C.sub.18 arylene, or C.sub.7 -C.sub.30 alkylarylene;R.sup.3 represents C.sub.1 -C.sub.24 alkyl, C.sub.3 -C.sub.24 cycloalkyl, C.sub.1 -C.sub.24 aryl, or C.sub.7 -C.sub.30 alkylaryl;R.sup.

Abstract: Chlorine-free, non-drying copolymer of isobutene with C.sub.4 -C.sub.10 -dienes having isolated or conjugated double bonds and containing at least 60 mol % of terminal double bonds, and a process for their preparation.

Abstract: An oligomer is made by contacting an olefinic monomer with a catalyst comprising boron trifluoride, an alcohol alkoxylate, and a ketone. In one embodiment, the olefinic monomer is a straight-chain, .alpha.-olefinic monomer containing from 8 to 12 carbon atoms, the alcohol alkoxylate is 2-ethoxyethanol, the ketone is methyl ethyl ketone, and the oligomer product has a kinematic viscosity at 100.degree. C. of less than 1.7 cSt. Before removal of unreacted monomer, the oligomer product is at least 50 wt. % dimer, at least 80 wt. % dimer plus trimer, and less than 3.25 wt. % tetramer and greater.

Abstract: A synthetic oil is made by a process comprising the steps of (a) reacting a vinylidene olefin in the presence of a catalyst to form an intermediate mixture which contains at least about 50 weight percent dimer of said vinylidene olefin, and (b) adding a vinyl olefin to said intermediate mixture and reacting said intermediate mixture and said vinyl olefin in the presence of a catalyst so as to form a product mixture which contains said dimer of said vinylidene olefin and a codimer of said added vinyl olefin with said vinylidene olefin.

Abstract: An oligomer is made by contacting a straight-chain, .alpha.-olefinic monomer with boron trifluoride and a hydroxy carbonyl promoter. The hydroxy carbonyl is preferably a .beta.-hydroxy-ketone, such as 4-hydroxy-4-methyl-2-pentanone. A second promoter can be used in conjunction with the boron trifluoride and the hydroxy carbonyl promoter. Possible secondary promoters include aldehydes, alcohols, alcohol alkoxylates, carboxylic acids, ethers, ketones, and their mixtures. Preferably the oligomer product has a kinematic viscosity at 100.degree. C. of less than 1.7 cSt; has a dimer to trimer and higher oligomer ratio of at least 1:1; and is at least 90 wt. % dimer and trimer of the monomer.

Abstract: Organic aluminoxy compounds are prepared by reacting an organo boronic acid with a trihydrocarbyl aluminum compound. The resulting products are suitable as components for catalyst systems for the polymerization of olefins.

Abstract: A process for making an .alpha.-olefin oligomer comprises contacting a C.sub.6 to C.sub.20 .alpha.-olefin monomer with a catalyst which includes boron trifluoride, a protic promotor and a polyether.

Abstract: A crystalline low-aluminum boron beta zeolite is prepared using a diquaternary ion as a template.

Abstract: A process for the polymerization of ethylene or a mixture comprising ethylene and one or more alpha-olefins and, optionally, a diene, comprising passing, under polymerization conditions, the aforementioned monomer(s) into contact with a catalyst system comprising:(a) the reaction product of(i) a titanium based catalyst precursor having the formula Mg.sub.a Ti(OR).sub.b X.sub.c (ED).sub.d whereinED is an inside electron donor comprising a mixture of (A) about 1 to about 80 mole percent of an alkyl, alkoxy, aryl, or aryloxy phosphine oxide, or mixtures thereof, and (B) about 20 to about 99 mole percent of an organic ester, ether, or ketone, or mixtures thereof, said phosphine oxide also being present in a molar ratio of phosphine oxide to titanium of 0.

Abstract: A process for preparing highly reactive polyisobutenes with a content of terminal vinylidene groups of more than 80 mol % and an average molecular weight of 500-5000 Dalton by the cationic polymerization of isobutene or isobutene-containing hydrocarbon feeds in liquid phase with the aid of boron trifluoride as catalyst and at from 0.degree. C. to -60.degree. C., comprises polymerizing in the presence of secondary alcohols with 3-20 carbon atoms and/or ethers with 2-20 carbon atoms.

Abstract: A synthetic oil is made by a process comprising (a) isomerizing at least a portion of a vinylidene olefin feed to form an intermediate which contains tri-substituted olefin and (b) reacting said intermediate and at least one vinyl olefin in the presence of a catalyst to form a synthetic oil which comprises a co-dimer of said vinylidene olefin and said vinyl olefin.

Abstract: A process for the preparation of olefins of the general formula (CH.sub.2 --CH.sub.2).sub.p --CH.dbd.CH.sub.2 in which formula R is a hydrocarbyl group and p is an integer of at least 1, comprising reacting ethene with at least one additional alpha olefin of the general formula R--CH.dbd.CH.sub.2 under oligomerization conditions in the presence of a catalyst system comprising a first component which is a bis(cyclopentadienyl) Group IVA metal compound containing a substituent which is attached to the metal and which is capable of reacting with a cation, and a second component which is a compound having a bulky anion containing a plurality of boron atoms and which is substantially non-coordinating under the reaction conditions and a cation, and recovering an oligomeric product comprising linear olefins of the general formula R--(CH.sub.2 --CH.sub.2).sub.p --CH.dbd.CH.sub.

Abstract: This invention describes highly reactive polymers obtained from lower monomers. The polymers are particularly useful in alkylation reactions.

Abstract: The invention relates to a method for removing a boron trifluoride from the exhaust gases of a vacuum pump, which gases have been obtained when polymerizing .alpha.-olefines by using a BF.sub.3 -alcohol complex as a catalyst. In a vacuum distillation, the underpressure is achieved by means of a pump sealed with a fluid ring or by means of fluid jet with a torque or ejector pump, possibly assisted by a mechanical blaster, such as a propellant circulating pump. In this pump, the fluid ring or the fluid jet is formed by a cocatalyst forming a complex with the BF.sub.3 catalyst, which cocatalyst is an alcohol, preferably butanol.

Abstract: An ethylene oligomerization process is provided wherein ethylene is contacted with a nickel(II) halide compound, a phosphine compound, and a carboxylate compound in a solvent to produce a precursor reaction mixture, followed by contacting ethylene with the precursor reaction mixture and a borohydride compound to produce a product reaction mixture comprising the desired oligomerization product.

Abstract: A process for the metathesis of olefins and functionalized olefins on Re.sub.2 O.sub.7 /Al.sub.2 O.sub.3 -containing catalysts, which comprises effecting metathesis reaction in the presence of one or more halogen-free organoaluminum compounds as activators.

Abstract: The process of the present invention relates to a simplified method for the removal of halogen containing catalytic residues from olefin polymerization products. More specifically, the present invention employs as a treating agent, a quaternary ammonium salt, to facilitate removal of greater than 95% of catalytic residues in a single caustic or water wash with less than 15 minutes of settling time required after the wash.

Abstract: A process for producing an olefin oligomer by the polymerization of an olefin in the presence of boron trifluoride as a catalyst, and further in the co-presence of water and/or an alcohol and a carboxylic acid anhydride as a co-catalyst. The process has advantages that (i) olefin oligomers having a low viscosity can be produced at high yields, (ii) the production efficiency can be improved by decreasing the time required for the reaction, (iii) the amount of the co-catalyst required can be decreased, and (iv) the viscosity of an olefin oligomer to be obtained can be freely controlled by changing the amounts of the olefin, the catalyst, the co-catalyst, etc.

Abstract: A catalyst for the metathesis of olefins and functionalized olefins, which contains a compound having the formula B.sub.2 O.sub.3 -Re.sub.2 O.sub.7 /Al.sub.2 O.sub.3 -SiO.sub.2.

Abstract: A method for producing polymers with narrow molecular weight distribution which involves combining (1) an initiator component of the formula ##STR1## in which R.sub.1, R.sub.2, and R.sub.3 are alkyl, aryl, or aralkyl groups, and can be the same or different, and X is an acetate, etherate, a hydroxyl group, or a halogen, and i is a positive whole number, (2) a Lewis acid of the formula MX.sub.n in which M is titanium, aluminum, boron, or tin, X is a halogen, and n is a positive whole number, (3) an electron donor component having an electron donor number of from at least about 25 to no more than about 50, (4) a solvent for the preceding and (5) a hydrocarbon monomer component.

Abstract: A catalyst for the metathesis of olefins and functionalized olefins, which contains a compound having the formula B.sub.2 O.sub.3 --Re.sub.2 O.sub.7 /Al.sub.2 O.sub.3 --SiO.sub.2.

Abstract: A process for removing vinylidene olefin from an olefin mixture containing about 1 to 55 mole percent vinylidene olefin, 0 to 20 mole percent internal olefin and the balance vinyl olefin, said process comprising:(a) reacting said olefin mixture in the presence of a BF.sub.3 /phosphorus acid catalyst system so as to selectively dimerize vinylidene olefins, and(b) separating said vinyl olefin and internal olefin from the dimerized vinylidene olefin to produce an olefin product having a reduced vinylidene olefin content and an increased vinyl olefin content compared to said starting olefin mixture.

Abstract: Vinylidene olefin is removed from an olefin mixture containing about 1 to 55 mole percent vinylidene olefin, 0 to 20 mole percent internal olefin, and the balance vinyl olefin, by:(A) reacting the olefin mixture in the presence of a BF.sub.3 -water and/or organic promoter catalyst system so as to selectively dimerize said vinylidene olefin, and(B) separating said vinyl olefin and internal olefin from the dimerized vinylidene olefin to produce an olefin product having a reduced vinylidene olefin content compared to said olefin mixture.