WO1999037692A1 - Katalytisch beschleunigte gasphasenreaktionen - Google Patents
Katalytisch beschleunigte gasphasenreaktionen Download PDFInfo
- Publication number
- WO1999037692A1 WO1999037692A1 PCT/CH1999/000029 CH9900029W WO9937692A1 WO 1999037692 A1 WO1999037692 A1 WO 1999037692A1 CH 9900029 W CH9900029 W CH 9900029W WO 9937692 A1 WO9937692 A1 WO 9937692A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- reaction
- catalyst
- solvent
- gas phase
- reaction mixture
- Prior art date
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Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G61/00—Macromolecular compounds obtained by reactions forming a carbon-to-carbon link in the main chain of the macromolecule
- C08G61/02—Macromolecular compounds containing only carbon atoms in the main chain of the macromolecule, e.g. polyxylylenes
- C08G61/04—Macromolecular compounds containing only carbon atoms in the main chain of the macromolecule, e.g. polyxylylenes only aliphatic carbon atoms
- C08G61/06—Macromolecular compounds containing only carbon atoms in the main chain of the macromolecule, e.g. polyxylylenes only aliphatic carbon atoms prepared by ring-opening of carbocyclic compounds
- C08G61/08—Macromolecular compounds containing only carbon atoms in the main chain of the macromolecule, e.g. polyxylylenes only aliphatic carbon atoms prepared by ring-opening of carbocyclic compounds of carbocyclic compounds containing one or more carbon-to-carbon double bonds in the ring
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J12/00—Chemical processes in general for reacting gaseous media with gaseous media; Apparatus specially adapted therefor
- B01J12/002—Chemical processes in general for reacting gaseous media with gaseous media; Apparatus specially adapted therefor carried out in the plasma state
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J19/00—Chemical, physical or physico-chemical processes in general; Their relevant apparatus
- B01J19/08—Processes employing the direct application of electric or wave energy, or particle radiation; Apparatus therefor
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F10/00—Homopolymers and copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J2219/00—Chemical, physical or physico-chemical processes in general; Their relevant apparatus
- B01J2219/08—Processes employing the direct application of electric or wave energy, or particle radiation; Apparatus therefor
- B01J2219/0894—Processes carried out in the presence of a plasma
- B01J2219/0896—Cold plasma
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F110/00—Homopolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond
- C08F110/04—Monomers containing three or four carbon atoms
- C08F110/08—Butenes
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F4/00—Polymerisation catalysts
- C08F4/42—Metals; Metal hydrides; Metallo-organic compounds; Use thereof as catalyst precursors
- C08F4/44—Metals; Metal hydrides; Metallo-organic compounds; Use thereof as catalyst precursors selected from light metals, zinc, cadmium, mercury, copper, silver, gold, boron, gallium, indium, thallium, rare earths or actinides
- C08F4/60—Metals; Metal hydrides; Metallo-organic compounds; Use thereof as catalyst precursors selected from light metals, zinc, cadmium, mercury, copper, silver, gold, boron, gallium, indium, thallium, rare earths or actinides together with refractory metals, iron group metals, platinum group metals, manganese, rhenium technetium or compounds thereof
- C08F4/62—Refractory metals or compounds thereof
- C08F4/64—Titanium, zirconium, hafnium or compounds thereof
- C08F4/659—Component covered by group C08F4/64 containing a transition metal-carbon bond
- C08F4/6592—Component covered by group C08F4/64 containing a transition metal-carbon bond containing at least one cyclopentadienyl ring, condensed or not, e.g. an indenyl or a fluorenyl ring
- C08F4/65922—Component covered by group C08F4/64 containing a transition metal-carbon bond containing at least one cyclopentadienyl ring, condensed or not, e.g. an indenyl or a fluorenyl ring containing at least two cyclopentadienyl rings, fused or not
- C08F4/65925—Component covered by group C08F4/64 containing a transition metal-carbon bond containing at least one cyclopentadienyl ring, condensed or not, e.g. an indenyl or a fluorenyl ring containing at least two cyclopentadienyl rings, fused or not two cyclopentadienyl rings being mutually non-bridged
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S526/00—Synthetic resins or natural rubbers -- part of the class 520 series
- Y10S526/901—Monomer polymerized in vapor state in presence of transition metal containing catalyst
Definitions
- the present invention relates to a process for carrying out an anionically or cationically catalytically accelerated gas phase reaction, a process for carrying out a catalytically accelerated gas phase polymerization and uses of the processes and polymers prepared by the process according to the invention.
- the catalysts are generally arranged on support substances and thereby added.
- the carrier together with the catalyst is kept in the gaseous reaction mixture by means of a fluidized bed.
- catalysts which are arranged on carrier substances are used, so-called metal locene-based catalysts being used recently, which are arranged, inter alia, on silica gel or magnesium chloride as carrier particles.
- the reaction rate usually has to be negatively influenced by the presence of the solvent and the counterions.
- the solvent can react partially with the catalyst or form complexes by addition to the active anion or cation, as a result of which the activity of the catalyst is reduced.
- the solvent also destroys a favorable electrostatic interaction that exists in the gas phase.
- these catalysts are so-called Ziegler-Natta catalysts or catalysts suitable for carrying out so-called metathesis processes.
- the object is achieved by a method according to the wording, in particular according to claim 1.
- the active anion or the active cation which forms the catalyst, as a free anion or cation without a corresponding counterion and at least to a large extent - 3 -
- the substance forming the catalyst is first introduced into a solvent or activated in solution and then the solvent and the counterion are largely removed before being introduced into the gaseous reaction mixture.
- Electrospray ionization, thermospray ion evaporation or with so-called atmospheric pressure ionization is introduced.
- So-called Ziegler-Natta catalysts or metallocene catalysts are particularly suitable as catalysts, which are first dissolved and activated in a suitable solvent.
- the catalyst thus dissolved and activated is then sprayed by means of electrospray, thermospray or ion evaporation or by means of atmospheric pressure ionization, the spraying generally being carried out under high pressure, while simultaneously enveloping the spray cloud in an inert gas such as nitrogen or Noble gas.
- an inert gas such as nitrogen or Noble gas.
- the anion or cation now isolated in this way which serves as a catalyst for the reaction, is then introduced into a reaction space in which the gaseous reaction mixture or the gaseous monomer to be polymerized is arranged. It is it is possible to arrange several reaction stages or spaces one after the other in order to carry out subsequent chain-forming polymerization reactions, in particular in the case of the polymerization.
- FIG. 1 shows an electrospray arrangement which can generally be found in mass spectrometers, a slightly modified Finnigan-MAT-TSQ7000 electrospray tandem mass spectrometer, with an octopole-quadrupole-octopole-quadrupole (for carrying out the experiments described below, 01 / Q1 / 02 / Q2) - arrangement equipped, was used, similarly described by Armentrout et al. (Ref. 1) with directed ion beams, but with an electrospray instead of a conventional ion source (see Ref. 2).
- FIG. 1 shows an electron spray ion source 1, which is formed by a cylindrical electrode 3.
- the solvent loaded with the catalyst is introduced into a first region A via a hypodermic needle or a fine inlet tube 5, the sprayed solvent with catalyst being shown schematically by means of a spray cloud 13.
- This hypodermic needle is encased by inlet pipes 5 for a protective gas, such as nitrogen or an inert gas, which is sprayed with the solvent when sprayed.
- a conditioning gas is introduced via lines 9 into the first area A in order to condition the sprayed solvent, including the activated catalyst, to a certain temperature.
- a voltage is applied in the area of the discharge nozzle 11 of the cylindrical electrode 3, in the order of magnitude from 0 to +8 kV or in the order of magnitude from 0 to -8 kV.
- the catalyst electrospray mist is passed through a heated capillary 13, at the end of which a tubular lens 17 is arranged, on which a voltage of approximately 0 to +200 or 0 to -200 V is applied. Via this tubular lens 17, the electrospray mist is discharged into a subsequent area B, in which a vacuum is applied in order to suck off evaporated solvent, for example via a separating pump 19.
- a separator 21 which is grounded, the counterion is also collected, so that through the passage opening 23 arranged in the separator only the anion or cation responsible for the catalytic acceleration can pass into a first reaction area C, in which one first octopole arrangement 25 is provided. In this first octopole area, the inert gas or protective gas or conditioning gas is displaced by the reaction gas, so that the catalytically accelerated gas phase reaction is initiated.
- an analytical area D which has a quadrupole arrangement typical of a mass spectrometer for the analysis of the reaction mixture.
- the gas phase reaction is continued in a subsequent reaction region E, again having an octopole arrangement 29, for example in order to generate oligomers.
- the reaction products are analyzed again in the final, subsequent analysis area F, again having a quadrupole arrangement 31.
- a so-called dinode and an electrical amplifier 33 are arranged at the end of the reaction arrangement.
- This example is about the addition of several olefin units to an isolated alkyl-zirconocene cation in the gas phase.
- the addition of 1-butene to free cations takes place at a diffusion-controlled rate which is 10 7 to 10 8 times faster than the corresponding solvent phase addition, in which the metallocene cation is part of an ion pair, often with one or more coordination - ligands (eg solvents).
- the observed reaction corresponds to the repeated chain reaction steps of a Ziegler-Natta polymerization (ref. 3), which has been well investigated in solution with similar homogeneous catalysts, and has never been previously observed in mass spectrometer studies of isolated ions.
- meters can be regarded as a reasonable model for the industrial process and can therefore provide suitable analytical and mechanistic options.
- Hydrogen loss and CH 4 loss products which are believed to have ⁇ -allyl structures, are catalytically inactive in Ziegler-Natta polymerization. Accordingly, the addition of more than one unit of an olefin could not be observed.
- II is formed as a chemically activated species, which behaves best entropically when there is no collision, namely through dissociation.
- Enthalpy-favored reactions e.g. Addition reactions, mostly take place under high pressure or condensed phase
- the chemistry subsequent to the incorporation of an olefin unit in the metal-carbon bond corresponds to the condensed-phase and high-pressure gas-phase chemistry, but with an extraordinary increase in speed by a factor of 10 a to 10 7 , which in large-scale manufacturing processes of stereo-uniform high -performance polyolefins is used.
- Example 2 Olefin metathesis and ring opening metathesis polymerization using an electrosprayed ruthenium-carbene complex in the gas phase.
- the new complex VIII had the mass of an adduct of V and norbornene, as one would expect for the product of a one-step ring opening metathesis polymerization reaction (ROMP). Mass selection of VIII and collision in the second octopole region with either argon or norbornene led to the loss of the norbornene mass from the ion and presumably to the reformation of V.
- Electrospray ionization of medium to large organometallic complexes has only recently been described (Ref. 15), but has not been systematically linked (Ref. 16) to the large number of ion-molecule reaction techniques that are associated with small gas phases -organometallic ions (Lit.
- the absolute reaction rate is the exception to the similarities of the gas phase and solvent phase reactions.
- the olefin metathesis and ring opening metathesis polymerization reactions described here are up to a factor of approximately 10 7 relative to the solvent phase rate in the work of Grubbs ( Lit. 1 9) accelerated.
- the effect is most likely due to the ion dipole or ion induced dipole interactions - 19 -
- the present invention is naturally not intended to refer to the use of metallocene catalysts for carrying out polymerization reactions or to Ziegler-Natta catalysts in connection with the implementation of metathesis or metathesis ring opening Polymerization reactions may be limited.
- the two examples only serve to explain the present invention in more detail and also to illustrate the analogy of the reactions by means of comparisons with catalysts correspondingly applied to support substances or with catalysts present in solutions and thus to prove that the anionic or ka ionic catalysts favor the corresponding gas reactions catalytically.
- the choice of the inert gas and the conditioning it depends, for example, whether the solvent can be removed completely or whether, for example, traces of the solvent still adhere to the catalyst. It is essential to the invention that the free anion or free cation, which serves as a catalyst for accelerating the gas phase reaction, is introduced into the gaseous reaction mixture without a counter ion and largely without solvent. This can be done, for example, by means of electrospray, by means of thermal spray or by means of atmospheric pressure ionization. - 22 -
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- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- General Health & Medical Sciences (AREA)
- Toxicology (AREA)
- Physics & Mathematics (AREA)
- Engineering & Computer Science (AREA)
- Plasma & Fusion (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Catalysts (AREA)
- Polyoxymethylene Polymers And Polymers With Carbon-To-Carbon Bonds (AREA)
Abstract
Description
Claims
Priority Applications (7)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE59905975T DE59905975D1 (de) | 1998-01-23 | 1999-01-22 | Katalytisch beschleunigte gasphasenreaktionen |
AU19584/99A AU1958499A (en) | 1998-01-23 | 1999-01-22 | Catalytically accelerated gaseous phase reactions |
AT99900429T ATE243224T1 (de) | 1998-01-23 | 1999-01-22 | Katalytisch beschleunigte gasphasenreaktionen |
JP53770299A JP2001517266A (ja) | 1998-01-23 | 1999-01-22 | 触媒により促進される気相反応 |
EP99900429A EP0970132B1 (de) | 1998-01-23 | 1999-01-22 | Katalytisch beschleunigte gasphasenreaktionen |
US09/400,128 US6555630B1 (en) | 1998-01-23 | 1999-09-21 | Catalytically accelerated gaseous phase reactions |
US10/357,764 US6777507B2 (en) | 1998-01-23 | 2003-02-03 | Catalytically accelerated gas phase reactions |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CH16298 | 1998-01-23 | ||
CH162/98 | 1998-01-23 |
Related Child Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US09/400,128 Continuation US6555630B1 (en) | 1998-01-23 | 1999-09-21 | Catalytically accelerated gaseous phase reactions |
Publications (1)
Publication Number | Publication Date |
---|---|
WO1999037692A1 true WO1999037692A1 (de) | 1999-07-29 |
Family
ID=4180678
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/CH1999/000029 WO1999037692A1 (de) | 1998-01-23 | 1999-01-22 | Katalytisch beschleunigte gasphasenreaktionen |
Country Status (7)
Country | Link |
---|---|
US (2) | US6555630B1 (de) |
EP (1) | EP0970132B1 (de) |
JP (1) | JP2001517266A (de) |
AT (1) | ATE243224T1 (de) |
AU (1) | AU1958499A (de) |
DE (1) | DE59905975D1 (de) |
WO (1) | WO1999037692A1 (de) |
Families Citing this family (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US7159015B2 (en) * | 2001-11-16 | 2007-01-02 | Sun Microsystems, Inc. | Method and apparatus for managing configuration information in a distributed computer system |
AU2003227182A1 (en) * | 2002-03-29 | 2003-10-13 | Mitsui Chemicals, Inc. | Method of recycling waste gas in polymer production plant |
KR100609564B1 (ko) | 2005-06-14 | 2006-08-08 | 금호석유화학 주식회사 | 기체혼합물을 중합 활성화제로 이용하는 고리형 올레핀화합물의 개환중합 방법 |
EP2550672A4 (de) * | 2010-03-24 | 2016-03-16 | Athula Buddhagosha Attygalle | Verfahren zur herstellung von gasphasen-metallanionen |
US9147844B2 (en) * | 2012-08-01 | 2015-09-29 | California Institute Of Technology | Solvent-free enyne metathesis polymerization |
US9234985B2 (en) | 2012-08-01 | 2016-01-12 | California Institute Of Technology | Birefringent polymer brush structures formed by surface initiated ring-opening metathesis polymerization |
Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE2835625A1 (de) * | 1978-02-28 | 1979-09-06 | Univ California | Polymerisationsverfahren |
US4212719A (en) * | 1978-08-18 | 1980-07-15 | The Regents Of The University Of California | Method of plasma initiated polymerization |
EP0277003A1 (de) * | 1987-01-30 | 1988-08-03 | Exxon Chemical Patents Inc. | Katalysatoren, Verfahren zur Herstellung derselben und Polymerisationsverfahren, unter Anwendung derselben |
US4835230A (en) * | 1988-10-17 | 1989-05-30 | Hercules Incorporated | Use of a cationic polymerization initiator in the preparation of thermoset polymer |
-
1999
- 1999-01-22 WO PCT/CH1999/000029 patent/WO1999037692A1/de active IP Right Grant
- 1999-01-22 JP JP53770299A patent/JP2001517266A/ja not_active Ceased
- 1999-01-22 AU AU19584/99A patent/AU1958499A/en not_active Abandoned
- 1999-01-22 DE DE59905975T patent/DE59905975D1/de not_active Expired - Fee Related
- 1999-01-22 AT AT99900429T patent/ATE243224T1/de not_active IP Right Cessation
- 1999-01-22 EP EP99900429A patent/EP0970132B1/de not_active Expired - Lifetime
- 1999-09-21 US US09/400,128 patent/US6555630B1/en not_active Expired - Fee Related
-
2003
- 2003-02-03 US US10/357,764 patent/US6777507B2/en not_active Expired - Fee Related
Patent Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE2835625A1 (de) * | 1978-02-28 | 1979-09-06 | Univ California | Polymerisationsverfahren |
US4212719A (en) * | 1978-08-18 | 1980-07-15 | The Regents Of The University Of California | Method of plasma initiated polymerization |
EP0277003A1 (de) * | 1987-01-30 | 1988-08-03 | Exxon Chemical Patents Inc. | Katalysatoren, Verfahren zur Herstellung derselben und Polymerisationsverfahren, unter Anwendung derselben |
US4835230A (en) * | 1988-10-17 | 1989-05-30 | Hercules Incorporated | Use of a cationic polymerization initiator in the preparation of thermoset polymer |
Non-Patent Citations (1)
Title |
---|
EHRLICH D J ET AL: "UV LASER PHOTODEPOSTION OF PATTERNED CATALYST FILMS FROM ADSORBATE MIXTURES", APPLIED PHYSICS LETTERS, vol. 46, no. 2, 15 January 1985 (1985-01-15), pages 198 - 200, XP000706377 * |
Also Published As
Publication number | Publication date |
---|---|
EP0970132A1 (de) | 2000-01-12 |
US20030144433A1 (en) | 2003-07-31 |
ATE243224T1 (de) | 2003-07-15 |
AU1958499A (en) | 1999-08-09 |
JP2001517266A (ja) | 2001-10-02 |
US6777507B2 (en) | 2004-08-17 |
EP0970132B1 (de) | 2003-06-18 |
US6555630B1 (en) | 2003-04-29 |
DE59905975D1 (de) | 2003-07-24 |
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