WO2011063937A1 - Process for the manufacture of propylene oxide - Google Patents
Process for the manufacture of propylene oxide Download PDFInfo
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- WO2011063937A1 WO2011063937A1 PCT/EP2010/007107 EP2010007107W WO2011063937A1 WO 2011063937 A1 WO2011063937 A1 WO 2011063937A1 EP 2010007107 W EP2010007107 W EP 2010007107W WO 2011063937 A1 WO2011063937 A1 WO 2011063937A1
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- propylene
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D301/00—Preparation of oxiranes
- C07D301/02—Synthesis of the oxirane ring
- C07D301/03—Synthesis of the oxirane ring by oxidation of unsaturated compounds, or of mixtures of unsaturated and saturated compounds
- C07D301/12—Synthesis of the oxirane ring by oxidation of unsaturated compounds, or of mixtures of unsaturated and saturated compounds with hydrogen peroxide or inorganic peroxides or peracids
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- 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
- B01J23/00—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00
- B01J23/16—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of arsenic, antimony, bismuth, vanadium, niobium, tantalum, polonium, chromium, molybdenum, tungsten, manganese, technetium or rhenium
- B01J23/32—Manganese, technetium or rhenium
- B01J23/34—Manganese
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- 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
- B01J31/00—Catalysts comprising hydrides, coordination complexes or organic compounds
- B01J31/02—Catalysts comprising hydrides, coordination complexes or organic compounds containing organic compounds or metal hydrides
- B01J31/12—Catalysts comprising hydrides, coordination complexes or organic compounds containing organic compounds or metal hydrides containing organo-metallic compounds or metal hydrides
-
- 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
- B01J31/00—Catalysts comprising hydrides, coordination complexes or organic compounds
- B01J31/16—Catalysts comprising hydrides, coordination complexes or organic compounds containing coordination complexes
- B01J31/18—Catalysts comprising hydrides, coordination complexes or organic compounds containing coordination complexes containing nitrogen, phosphorus, arsenic or antimony as complexing atoms, e.g. in pyridine ligands, or in resonance therewith, e.g. in isocyanide ligands C=N-R or as complexed central atoms
- B01J31/1805—Catalysts comprising hydrides, coordination complexes or organic compounds containing coordination complexes containing nitrogen, phosphorus, arsenic or antimony as complexing atoms, e.g. in pyridine ligands, or in resonance therewith, e.g. in isocyanide ligands C=N-R or as complexed central atoms the ligands containing nitrogen
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- 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
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
- Y02P20/00—Technologies relating to chemical industry
- Y02P20/50—Improvements relating to the production of bulk chemicals
- Y02P20/52—Improvements relating to the production of bulk chemicals using catalysts, e.g. selective catalysts
Definitions
- the invention relates to a process for the manufacture of propylene oxide ("PO") by catalytic oxidation of propylene using hydrogen peroxide and a manganese complex.
- PO propylene oxide
- PO is an important starting material in the chemical industry. It is applied in the production of polyether polyols that are used in making polyurethane plastics. Other uses of PO include the preparation of propylene glycol, propylene glycols ethers and propylene carbonate.
- the traditional route for the preparation of PO proceeds via the conversion of propylene to chloropropanols (known as "chlorohydrin process").
- chlorohydrin process The reaction produces a mixture of 1- chloro-2-propanol and 2-chloro-1-propanol which are then dehydrochlorinated into PO.
- Lime is used as chlorine absorber in this process. This method suffers from a relatively large amount of co-produced chloride salts.
- PO has been prepared by epoxidation with organic hydroperoxides.
- the hydroperoxides are produced by homogeneous oxidation of isobutane, ethyl benzene and cumene with molecular oxygen or air.
- Epoxidation is accomplished by either homogeneous Mo catalysts or heterogeneous Ti-based catalysts. This technology is used by Oxirane, Halcon, ARCO (isobutane and ethylbenzene), Shell (ethylbenzene), and Sumitomo (Cumene).
- WO2005000827 a process is known for the continuous epoxidation of propene with hydrogen peroxide in the presence of a titanium silicalite catalyst and a methanol solvent, wherein the catalyst is periodically regenerated by washing with a methanol solvent at a temperature of at least 00 °C and the epoxidation reaction is carried out for periods of more than 300 h between two regeneration steps.
- a process is known for the preparation of epoxides by epoxidation of olefinic compounds with hydrogen peroxide in the presence of a titanium silicalite as a catalyst.
- a base is introduced into the epoxidation reactor directly or as a mixture with one or more starting substances, under pH control.
- an aqueous-organic hydrogen peroxide solution with a pH in the range from 8 to 9 is employed and the epoxidation is carried out in a fixed bed reactor.
- solvent methanol is used as solvent methanol.
- a total of about 3-7 wt% of 1-methoxy-2-propanol (or propylene glycol monomethyl ether, PGME) and propylene glycol are commonly formed in the direct epoxidation of propylene in the mixed methanol and water as solvent.
- PGME propylene glycol monomethyl ether
- the use of organic solvents such as methanol-water or acetonitrile-water systems as solvent is disadvantage because these processes need recycle of organic solvents. Such processes require operating with complex distillation setups to separate the solvents from propylene and propylene oxide.
- Mn complexes of cyclic triamines
- TmTacn 1 ,4,7-trimethyl-1 ,4,7,- triazacyclononane
- EP0618202 (corresponding to US5329024).
- olefins such as 4-vinylbenzoic acid, styrylacetic acid, trans-3-hexenoic acid, trans-2-hexenoic acid and allyl alcohol are epoxidised by contact with a source of oxygen and a Mn complex, preferably a dinuclear manganese complex, in which the Mn is co-ordinated to a N-containing ligand such that there is a ratio of Mn to co-ordinated N atoms of 1 :3.
- the epoxidation process may be conducted in an aqueous media.
- the epoxidation When the epoxidation is conducted in an aqueous media, best results are obtained on olefins with water soluble groups.
- the epoxidation may be carried out in water, using a NaHC0 3 buffer with the pH adjusted to 9.0.
- This reference does not teach the epoxidation of propylene in water.
- Propylene is listed in a list separate from the olefins with water-soluble groups.
- this process utterly fails in the conversion of propylene into PO when using the recommended catalyst with the buffer in water as a solvent. A person starting from this reference, in the preparation of PO, would therefore not have considered the epoxidation of PO in water to be possible.
- a further reference of particular interest is WO2005095370.
- a catalytic process for the preparation of epoxides from alkenes is described, using a combination of transition metal salt, an inorganic promoter and an organic additive in absence of solvent or in the presence of a solvent with commercially available hydrogen peroxide.
- Styrene, indene, cyclohexene, a-pinene, and 1 ,2-dihydronaphthalene were epoxidized, typically in a mixture comprising dodecane, urea and water as the reaction medium.
- the present invention overcomes these disadvantages.
- the invention provides a process for the manufacture of propylene oxide ("PO") by catalytic oxidation (preferably epoxidation) of propylene with an oxidant wherein the catalytic oxidation is performed in an aqueous reaction medium, comprising water with less than 10% by volume of cosolvents, wherein a water-soluble manganese complex is used as oxidation catalyst,
- PO propylene oxide
- water-soluble manganese complex is a mononuclear species of the general formula (I):
- Mn is a manganese
- L or each L independently is a polydentate ligand
- each X independently is a coordinating species
- each ⁇ - ⁇ independently is a bridging
- Y is an non-coordinating counterion, and wherein the epoxidation is carried out at a pH in the range of from 1.5 to 6.0.
- the PO or part of the PO is isolated as gas phase, which comprises PO or a mixture of propylene and PO.
- gas phase which comprises PO or a mixture of propylene and PO.
- the catalyst comprises a manganese atom or a number of manganese atoms coordinated with a ligand or ligands.
- the manganese atom(s) may be in a II, III or IV oxidation state and be activated during the reaction.
- binuclear manganese complexes Of particular interest are binuclear manganese complexes. Suitable manganese complexes therefore include mononuclear species of the general formula (I):
- Mn is a manganese
- L or each L independently is a polydentate ligand, preferably a cyclic or acyclic compound containing 3 nitrogen atoms
- each X independently is a coordinating species and each ⁇ - ⁇ independently is a bridging coordinating species, selected from the group consisting of:
- Counterion Y may for instance be an anion selected from the group consisting of RO “ , CI “ , Br “ , I “ , F “ , S0 4 2” , RCOO “ , PF 6 “ , tosylate, triflate (CF 3 S0 3 ) and a combination thereof with R once again being a Ci to C 2 o radical selected from the group consisting of alkyl, cycloalkyl, aryl, benzyl and combination thereof.
- the type of anion is not very critical, although some anions are more preferred than others.
- a preferred counterion is CH 3 COO " .
- Ligands which are suitable for the present invention are acyclic compounds containing at least 7 atoms in the backbone or cyclic compounds containing at least 9 atoms in the ring, each having the nitrogen atoms separated by at least two carbon atoms.
- a preferred class of ligands is that based on (substituted) triazacyclononane ("Tacn").
- the prefer ligand is TmTacn (1 ,4,7-trimethyl-1 ,4,7,-triazacyclononane), which is commercially available, for instance, from Aldrich.
- TmTacn (1 ,4,7-trimethyl-1 ,4,7,-triazacyclononane
- Dinuclear manganese complexes are preferred, because of their greater activity and solubility in water.
- Preferred dinuclear manganese complexes are those of the formula [ ⁇ - ⁇ , wherein L and Y have the meaning identified above, preferably TmTacn as ligand, and CH 3 COO " as counterion.
- the manganese complex may be utilized directly or as adsorbed onto a solvent insoluble support surface.
- Illustrative but nonlimiting examples of such substrates are structured aluminosilicates (e.g. Zeolite A, faujasite and sodalite), amorphous aluminosilicates, silica, alumina, charcoal, microporous polymeric resins (e.g. polystyrene beads formed through high internal phase emulsion technology) and clays (especially layered clays such as hectorite and hydrotalcite).
- Relative weight ratios of the manganese complex to the support may range anywhere from about 10:1 to about 1 :10,000.
- the manganese complex is used in catalytically effective amounts.
- the catalyst is used in a molar ratio of catalyst (Mn) versus hydrogen peroxide of from 1 :10 to 1 :10,000,000, preferably of from 1 :20 to 1 :100,000, most preferably of from 1 :50 to 1 :50000.
- Mn catalyst
- An advantage of the current invention, using a water soluble manganese complex is that the catalyst essentially does not migrate to the organic phase.
- the aqueous reaction medium typically is a water phase containing propylene and/or propylene oxide and less than 10% by volume, preferably only minor amounts, if any, of other organic compounds.
- the reaction medium may contain minor amounts of co-solvents such as methanol and acetone and the like.
- the aqueous reaction medium therefore suitably comprises at least 90% by volume of water, preferably 95 v%, more preferably 99 v%, still more preferably 99,9 v% of water.
- the aqueous reaction medium (again, excluding any propylene and/or propylene oxide dissolved therein) is essentially a 100% water phase.
- the aqueous reaction medium will contain a buffer system so as to stabilize the pH.
- a buffer system so as to stabilize the pH.
- the aqueous reaction medium is suitably stabilized in a pH range of 1.5 to 6.0, whereas the preferred pH range is between 1.5 and 5.0 and the most preferred is between 2.0 and 4.0.
- the suitable or preferred range may be achieved by several known organic acid-salt combinations, with the preferred combination being based on oxalic acid-oxalate salt, or acetate acid-acetate salt (3.7 to 5.6) or oxalic acid-oxalate salt and acetic acid -acetate salt.
- the pH ratio may be varied from 2.0 to 6.0.
- this buffer may be used in a molar ratio to the catalyst of about 10: 1 , but the amounts may be varied broadly, e.g., ranging from 1 :1 to 100:1.
- the buffer may also modify the manganese complexes to form buffer modified bridging coordinating species ( ⁇ - ⁇ )'.
- bridging coordinating species made from buffer materials include [OOC- COOH] 1 -, [OOC-COOJ2-, [OOCC-R-CCOOHJ1-, [OOCC-R-CCOO]2-, and combinations thereof.
- the modified bridging coordinating species may comprise one or more of the available bridging coordinating specie positions in the structures of the manganese complexes described herein.
- the bridging coordinating species of [OOC- COOH] 1" may form two of the three bridging coordinating species of the manganese complex described herein in a solution having an oxalate oxalic acid-oxalate salt buffer.
- the aqueous reaction medium may also contain a phase transfer agent and/or a surfactant.
- phase transfer agents that may be used in the process of the invention include quaternary alkyl ammonium salts.
- surfactants that may be used in the process of the invention include non ionic surfactants such as Triton X100TM available from Union Carbide. It is believed to be beneficial that the aqueous reaction medium contains at least trace amounts of propylene. Although this is purely a hypothesis, it is believed that the presence of propylene allows the catalyst to remain active, whereas it is believed that without the presence of propylene and/or due to the presence of PO and/or oxidant without propylene present the activity of the active catalyst reduces.
- the reaction conditions for the catalytic oxidation may be quickly determined by a person skilled in the art.
- the epoxidation is carried out either under pressure or at atmospheric pressure.
- the reaction is believed to be exothermic, and cooling of the reaction medium may be required.
- the reaction is preferably carried out at temperatures anywhere from 5°C to 40°C, preferably from 5°C to 30°C.
- catalyst and oxidant are preferably combined (for reaction with the propylene) at a molar ratio of from 1 :100 to 1 :10,00,000, more preferably of from 1 :500 to 1 : 100,000, still more preferably of from 1 : 1000 to 1 :50,000.
- the molar ratio of propylene to hydrogen peroxide is very important in the process of the current invention. If too much hydrogen peroxide is used, then the selectivity towards the desired epoxide reduces due to the production of undesirable side-products, such as propan- 1 ,2-diol, or involves a significant waste of the oxidant. If not enough hydrogen peroxide is used, then the turnover number is suboptimal. This is therefore significantly different from bleaching conditions described in the prior art, where excessive amounts of hydrogen peroxide are used. Propylene may be preferably used in excess over the oxidant.
- the molar ratio of propylene to hydrogen peroxide may be in the range of from greater than 1 :2 to about 10:1 , such as from about 1 :1 to about 10:1 (or alternatively, from about 1 : 1.2 to about 2:1), for example, about 1 :1.
- the yield of epoxide with respect to peroxide utilization is from about 70% to about 99.7%, for example, about 89%.
- the conversion of propylene into PO is discussed hereinafter.
- the reaction may be performed in one phase, i.e., aqueous phase or a two layer system comprising an organic phase and an aqueous phase.
- propylene is fed at a rate that the concentration is above its maximum solubility in the reaction medium then depending on the reaction temperature and pressure, propylene will form a separate gas or liquid phase.
- propylene has a solubility (expressed in grams per liter water at 20°C) of about 0.4 g/L at a partial pressure of 1 bar.
- the solubility of the propylene may change under different partial pressure conditions when propylene is introduced as a gas phase or under the conditions described hereafter.
- propylene can form a separate gas phase.
- the propylene that leaves the reaction medium is preferably recycled.
- PO formed during the reaction may come out of the reaction medium as a gas as well (e.g. above 40° C and 1 Bar). This is advantageous in that the PO is stripped from the reaction mixture together with the recycled propylene gas.
- the PO is recovered from the process by cooling the recycled propylene. In that case PO will be removed from the process by condensation.
- other methods of PO removal as known by people skilled in the art, are not excluded from this invention.
- Such methods may be needed if the pressure and temperature conditions are sufficient to cause propylene to be present as a gas but insufficient to cause PO to come out.
- the propylene oxide then remains dissolved in the reaction medium or even forms a separate organic phase if the concentration exceeds solubility.
- propylene will be present as a separate organic phase.
- the PO formed during the reaction may be dissolved in the reaction medium, and/or dissolved in the propylene phase (organic phase). Reaction conditions where parts or the whole reaction mixture becomes super critical are also part of this invention.
- propylene is finely dispersed as a gas into the reaction medium, propylene being fed in excess and the excess propylene leaving the reaction medium as a gas to be recycled.
- reaction temperature and pressure, as well as the PO concentration are selected such that the PO formed during the reaction leaves the reaction medium as a gas. More preferably the PO leaves the reaction medium being stripped by the propylene recycle and the PO being recovered from the propylene recycle by means of condensation.
- reaction is carried out at temperatures in the range from 5°C and 40°C and at pressures in the range from 0.9 to 9 bar.
- the catalytic oxidation of the present invention is carried out preferably using hydrogen peroxide as oxidant.
- Other oxidants may be used, i.e. as precursor to the hydrogen peroxide, but given the availability and to reduce environmental impact hydrogen peroxide is the preferred oxidant.
- Hydrogen peroxide has strong oxidizing properties. As bleaching agent it is mostly used for bleaching paper. It is typically used in an aqueous solution. The concentration of hydrogen peroxide may vary, from 15% (e.g., consumer grade for bleaching hair) to 98% (propellant grade), with a preference for industrial grades varying from 20 to 60%, preferably from 30 to 50%.
- the oxidant is preferably added to the aqueous reaction medium at a rate about equal to the reaction rate of the catalytic oxidation.
- the catalytic oxidation may be performed in a batch process, in a continuous process or in a semi-continuous process. Indeed, the process may be modified in various aspects without departing from the gist of the invention.
- the catalytic oxidation may be performed in a common stirred tank reactor provided with a means of stirring. For instance, this may be a common explosion-proof blade agitator operating under an agitation speed of around 400 rpm.
- the catalyst, aqueous reaction medium and reactants may be added in batch, or the reactants may be added over a period of time. If hydrogen peroxide is added during the reaction, then it is added to either the (stirred) organic phase comprising the propylene or the (stirred) aqueous reaction medium.
- various recycling streams may be used to control the reaction conditions (maintained at a temperature of between 5°C and 40°C) and to optimize the production rate.
- Catalytic epoxidation of propylene was carried out with [(TmTacn) 2 Mn lv 2 ( -0) 3 ] 2+ (CH 3 COO " ) 2 as catalyst at 5° C in a four necked glass reactor facilitated with a mechanical stirrer, cooling jacket and a bottom valve.
- a sparger (porous) was used to send propylene into the reactor in the form of fine micro bubbles.
- the gas outlet of the reactor was connected to a cold trap to collect the product, propylene oxide. Water was used as solvent in the cold trap to collect the propylene oxide.
- An outlet was arranged to the cold trap for the safe passage of unreacted propylene, for re-use in the epoxidation.
- the molar ratio of propylene: hydrogen peroxide: catalyst: co-catalysts was excess propylene (excess propylene to hydrogen peroxide, thus, greater than 4300): 4300: 1 : 59.
- the aqueous solution in the reactor was analyzed to determine the residual level of H 2 0 2 .
- the unreacted hydrogen peroxide in the reactor was killed with Na 2 S0 3 .
- the aqueous solution in the reactor and the aqueous solution in the cold trap were analyzed by GC.
- the total amount of PO obtained from the two solutions was 15.5 g, which corresponds to 266 mmol for the theoretical maximum production of 300 mmol.
- the only by-product formed in the reaction was propan-1 ,2-diol, however at a negligible amount of 0.06 g (corresponding to 0.76 mmol).
- 0.06 wt% of the H 2 0 2 was left over in the reaction mixture corresponds to 6 mmol.
- the selectivity of propylene oxide is 99.7% and the yield of epoxide with respect to peroxide utilization is 89%.
- Catalytic epoxidation of propylene was carried out similar to example 1 above, however with [(TMTACN) 2 Mn IV 2(M-0) 3 ] 2+ (PF 6 )2 in the presence of NaHC0 3 buffer as mentioned in Example 1 of EP0618202 A1.
- Propylene gas was continuously send as fine micro bubbles into the reactor containing 300 mL of 0.1 M NaHC0 3 buffer and 0.008 M of [(TMTACN) 2 ⁇ - 0) 3 ] 2+ (PF 6 ) 2 catalyst. Reaction is initiated with the addition of 35 wt% hydrogen peroxide in water. Total 300 mmol of dilute H 2 0 2 was added at 10 mLJh flow rate for 2.8 h and the reaction is continued for 3 h.
- the aqueous solution in the reactor and the aqueous solution in the cold trap were analyzed by GC.
- the left over hydrogen peroxide in the reactor is found to be 92 mmol.
- the PO produced during the reaction was lower than 1 %.
- Total 208 mmol of H 2 0 2 was decomposed into the H 2 0 and 0 2 during the reaction of 3 h.
- Catalytic epoxidation of propylene was carried out similar to example 1 above, however with the in-situ catalyst system obtained by MnS0 4 , TmTacn in oxalate buffer as mentioned in Table 1 of the De Vos article in Tetrahedron Letters 39 (1998) 3221. It should be noted that a soluble catalyst system could be produced in-situ only when using acetonitrile as solvent. On the other hand, when the method was repeated using water as solvent, no soluble catalyst was formed.
- the PO produced during the reaction was 2.8 g of PO, which corresponds to 48 mmol and 0.04 mmol of propane-1 ,2- diol.
- the selectivity of propylene oxide is 99.9%.
- the yield of epoxide with respect to the added hydrogen peroxide is only 16%.
- Catalytic epoxidation of propylene was carried out similar to example 1 above, however with the catalyst system used in example 1 of WO 2005/095370, both with and without urea.
- Example 1 is an example in accordance with the present invention.
- the yield of epoxide with respect to the added hydrogen peroxide was 89% at 99.7% selectivity of PO.
- Major amount of the formed PO was present in the reaction mixture under the present experimental conditions and only small amount of PO was evaporated and collected in the cold trap.
- the catalyst system of EP0618202 is active in water for water-soluble olefins.
- a scouting experiment with propylene would teach a person skilled in the art that it is not suitable for water insoluble olefins like propylene. Rather, the catalyst system is active in the catalytic decomposition of H 2 0 2 .
- the catalyst system in comparative example 4 efficiently decomposed the large amount (260 mmol) of H 2 0 2 into H 2 0 and 0 2 .
- the reaction mixture in this system is not 100% water as it contains dodecane (5 wt% in water).
- Urea appears to help to improve the epoxidation, possibly by the formation of urea hydrogen peroxide, which then acts as an oxidant for the epoxidation.
- Use of (large amounts of) urea is simply not economic.
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Abstract
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Priority Applications (9)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US13/512,167 US8735613B2 (en) | 2009-11-27 | 2010-11-24 | Process for the manufacture of propylene oxide |
EP10784453.2A EP2504325B1 (en) | 2009-11-27 | 2010-11-24 | Process for the manufacture of propylene oxide |
ES10784453.2T ES2634528T3 (en) | 2009-11-27 | 2010-11-24 | Procedure for the manufacture of propylene oxide |
CN201080053349.1A CN102858758B (en) | 2009-11-27 | 2010-11-24 | For the manufacture of the method for propylene oxide |
JP2012540310A JP5558578B2 (en) | 2009-11-27 | 2010-11-24 | Propylene oxide production method |
KR1020127016479A KR101420948B1 (en) | 2009-11-27 | 2010-11-24 | Process for the manufacture of propylene oxide |
RU2012126638/04A RU2528385C2 (en) | 2009-11-27 | 2010-11-24 | Method of producing propylene oxide |
AU2010324184A AU2010324184B2 (en) | 2009-11-27 | 2010-11-24 | Process for the manufacture of propylene oxide |
BR112012012506-0A BR112012012506B1 (en) | 2009-11-27 | 2010-11-24 | PROCESS FOR THE MANUFACTURE OF PROPYLENE OXIDE |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
EP09075528A EP2343288A1 (en) | 2009-11-27 | 2009-11-27 | Process for the manufacture of propylene oxide |
EP09075528.1 | 2009-11-27 |
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WO2011063937A1 true WO2011063937A1 (en) | 2011-06-03 |
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PCT/EP2010/007107 WO2011063937A1 (en) | 2009-11-27 | 2010-11-24 | Process for the manufacture of propylene oxide |
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US (1) | US8735613B2 (en) |
EP (2) | EP2343288A1 (en) |
JP (1) | JP5558578B2 (en) |
KR (1) | KR101420948B1 (en) |
CN (1) | CN102858758B (en) |
AU (1) | AU2010324184B2 (en) |
BR (1) | BR112012012506B1 (en) |
ES (1) | ES2634528T3 (en) |
HU (1) | HUE034449T2 (en) |
MY (1) | MY157588A (en) |
RU (1) | RU2528385C2 (en) |
TW (1) | TWI430840B (en) |
WO (1) | WO2011063937A1 (en) |
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WO2016131858A1 (en) * | 2015-02-17 | 2016-08-25 | Evonik Degussa Gmbh | Method for the epoxidation of an olefin with hydrogen peroxide |
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US10428035B2 (en) | 2015-11-26 | 2019-10-01 | Evonik Degussa Gmbh | Process for the epoxidation of an olefin |
US10676450B2 (en) | 2016-01-19 | 2020-06-09 | Evonik Operations Gmbh | Process for the epoxidation of an olefin |
EP4063355A1 (en) | 2021-03-22 | 2022-09-28 | Evonik Operations GmbH | Integrated process and plant for making styrene and propene oxide |
Families Citing this family (1)
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WO2020245621A1 (en) * | 2019-06-04 | 2020-12-10 | Toyota Motor Europe | Supported oxide nh3-scr catalysts with dual site surface species and synthesis processes |
Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5329024A (en) | 1993-03-30 | 1994-07-12 | National Starch And Chemical Investment Holding Corporation | Epoxidation of olefins via certain manganese complexes |
US20020004606A1 (en) | 1999-09-18 | 2002-01-10 | Georg Thiele | Process for the preparation of epoxides from olefins |
WO2005000827A1 (en) | 2003-06-18 | 2005-01-06 | Degussa Ag | Process for the epoxidation of propene |
WO2005095370A1 (en) | 2004-03-31 | 2005-10-13 | Council Of Scientific & Industrial Research | An improved catalytic process for the preparation of epoxides from alkenes |
EP2149569A1 (en) | 2008-08-01 | 2010-02-03 | Hexion Specialty Chemicals Research Belgium S.A. | Process for the manufacture of a 1,2-Epoxide |
Family Cites Families (45)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4021454A (en) | 1971-08-19 | 1977-05-03 | Shell Oil Company | Olefin epoxidation |
US4038291A (en) | 1975-04-04 | 1977-07-26 | Texaco Development Corporation | Boride catalyst for epoxidizing olefinic compounds |
US4127594A (en) | 1978-02-21 | 1978-11-28 | Shell Oil Company | Selective hydrogenation of olefinic impurities in epichlorohydrin |
FR2419938A1 (en) * | 1978-03-13 | 1979-10-12 | Charbonnages Ste Chimique | Styrene oxide prepn. - by reaction of styrene with oxygenated water in presence of acetonitrile and di:sodium phosphate |
DE3731690C1 (en) | 1987-09-21 | 1989-01-19 | Degussa | Process for the catalytic epoxidation of olefins with hydrogen peroxide |
ES2100844T3 (en) | 1988-12-02 | 1997-07-01 | Hoechst Ag | COMPLEX COMBINATIONS WITH SULPHONATED PHENYLPHOSPHANES CONTENT. |
DE69125310T2 (en) | 1990-05-21 | 1997-07-03 | Unilever Nv | Bleach activation |
EP0522817A1 (en) | 1991-07-11 | 1993-01-13 | Unilever Plc | Process for preparing manganese complexes |
US5153161A (en) | 1991-11-26 | 1992-10-06 | Lever Brothers Company, Division Of Conopco, Inc. | Synthesis of manganese oxidation catalyst |
US5256779A (en) | 1992-06-18 | 1993-10-26 | Lever Brothers Company, Division Of Conopco, Inc. | Synthesis of manganese oxidation catalyst |
US5429769A (en) | 1993-07-26 | 1995-07-04 | Lever Brothers Company, Division Of Conopco, Inc. | Peroxycarboxylic acids and manganese complex catalysts |
US5532389A (en) | 1993-11-23 | 1996-07-02 | The Dow Chemical Company | Process for preparing alkylene oxides |
UA48945C2 (en) * | 1994-02-04 | 2002-09-16 | Смітклайн Бічам Плс | Process for epoxidising of prochiral olefin, catalyst for this process and method for production of catalyst |
DE19523890C1 (en) * | 1995-06-30 | 1996-11-28 | Hoechst Ag | Process for the preparation of chiral epoxides with chiral manganese triazanonane complexes as oxidation catalysts |
DE19533331A1 (en) | 1995-09-11 | 1997-03-13 | Basf Ag | Metal complexes containing peroxo groups with amine oxide or phosphine oxide ligands as epoxidation catalysts |
DE19600160C1 (en) * | 1996-01-04 | 1997-05-28 | Hoechst Ag | Process for the oxidation of vinyl compounds in the presence of bis- and tris (mu-oxo) -di-manganese complex salts as a catalyst |
US5833755A (en) | 1996-03-25 | 1998-11-10 | National Starch And Chemical Investment Holding Corporation | Starch degradation using metal-based coordination complexes |
DE19620241A1 (en) | 1996-05-20 | 1997-11-27 | Patt R Prof Dr | Process for delignifying pulps and using a catalyst |
DE19723950A1 (en) * | 1997-06-06 | 1998-12-10 | Basf Ag | Process for the oxidation of an organic compound having at least one C-C double bond |
BE1011456A3 (en) | 1997-09-18 | 1999-09-07 | Solvay | METHOD OF MANUFACTURING an oxirane. |
BE1011576A3 (en) | 1997-11-27 | 1999-11-09 | Solvay | Epichlorohydrin based product and method for manufacturing this product. |
US6500968B2 (en) | 1998-08-26 | 2002-12-31 | Hydrocarbon Technologies, Inc. | Process for selective oxidation of organic feedstocks with hydrogen peroxide |
DE19923121A1 (en) | 1999-05-19 | 2000-11-23 | Basf Ag | Hydrogen peroxide oxidation of primary alcohols to give aldehydes and carboxylic acids uses a catalyst containing a manganese salt, a 1,4,7-tri-(1-20C alkyl)-1,4,7-triazacyclononane and a co-ligand |
US6087513A (en) | 1999-05-21 | 2000-07-11 | The Dow Chemical Company | Epoxidation process for aryl allyl ethers |
DE19936547A1 (en) | 1999-08-04 | 2001-02-15 | Basf Ag | Process for the reaction of an organic compound with a hydroperoxide |
EP1122249A1 (en) | 2000-02-02 | 2001-08-08 | SOLVAY (Société Anonyme) | Process for producing oxiranes |
BR0108772A (en) | 2000-02-29 | 2002-11-26 | Unilever Nv | Bleaching composition, method for bleaching a substrate, and, binding |
JP2002145872A (en) | 2000-11-01 | 2002-05-22 | Maruzen Petrochem Co Ltd | Method of manufacturing epoxy compound |
FR2824558B1 (en) | 2001-05-14 | 2005-05-06 | Solvay | PROCESS FOR PRODUCING AN OXIRIN |
US6596883B2 (en) | 2001-08-23 | 2003-07-22 | Degussa Ag | Process for the epoxidation of olefins |
US6624318B1 (en) | 2002-05-30 | 2003-09-23 | Basf Aktiengesellschaft | Process for the epoxidation of an organic compound with oxygen or an oxygen-delivering compounds using catalysts containing metal-organic frame-work materials |
EP1403219A1 (en) | 2002-09-30 | 2004-03-31 | Degussa AG | Novel aqueous hydrogen peroxide solutions |
FR2846965B1 (en) | 2002-11-12 | 2006-10-13 | PROCESS FOR THE PRODUCTION OF 1,2-EPOXY-3-CHLOROPROPANE | |
FR2846964B1 (en) | 2002-11-12 | 2006-07-21 | PROCESS FOR THE PRODUCTION OF 1,2-EPOXY-3-CHLOROPROPANE | |
DE10343252A1 (en) | 2003-09-17 | 2005-04-21 | Basf Ag | Process for the preparation of bisepoxides and dithiols |
CA2608440C (en) | 2005-05-27 | 2014-01-07 | Unilever Plc | Process of bleaching with a preformed transition metal catalyst salt together with hydrogen peroxide |
CN1900071A (en) | 2005-07-21 | 2007-01-24 | 中国科学院大连化学物理研究所 | Process for preparing epoxy chloropropane |
US7615654B2 (en) | 2005-10-20 | 2009-11-10 | Lyondell Chemical Technology, L.P. | Direct epoxidation process |
MX2008016526A (en) | 2006-06-23 | 2009-01-19 | Dow Global Technologies Inc | Process for producing epoxides from olefinic compounds. |
KR100846435B1 (en) | 2006-12-22 | 2008-07-16 | 한화석유화학 주식회사 | Process for preparation of an oxirane |
WO2008087657A2 (en) | 2007-01-15 | 2008-07-24 | Aditya Birla Science & Technology Limited | A process for preparing epichlorohydrin |
WO2009063487A2 (en) | 2007-08-10 | 2009-05-22 | Aditya Birla Science & Technology Co. Ltd. | An improved process for manufacture of epoxides, particularly epichlorohydrin |
EP2149570A1 (en) | 2008-08-01 | 2010-02-03 | Hexion Specialty Chemicals Research Belgium S.A. | Process for the manufacture of epichlorohydrin using hydrogen peroxide and a manganese komplex |
WO2011062608A2 (en) | 2009-11-19 | 2011-05-26 | Dow Global Technologies, Inc. | Epoxidation of an olefin |
EP2354131A1 (en) * | 2010-02-02 | 2011-08-10 | Momentive Specialty Chemicals Research Belgium | Process for the manufacture of a 1,2-epoxide and a device for carrying out said process |
-
2009
- 2009-11-27 EP EP09075528A patent/EP2343288A1/en not_active Withdrawn
-
2010
- 2010-11-24 RU RU2012126638/04A patent/RU2528385C2/en not_active IP Right Cessation
- 2010-11-24 ES ES10784453.2T patent/ES2634528T3/en active Active
- 2010-11-24 HU HUE10784453A patent/HUE034449T2/en unknown
- 2010-11-24 MY MYPI2012002344A patent/MY157588A/en unknown
- 2010-11-24 AU AU2010324184A patent/AU2010324184B2/en not_active Ceased
- 2010-11-24 JP JP2012540310A patent/JP5558578B2/en not_active Expired - Fee Related
- 2010-11-24 WO PCT/EP2010/007107 patent/WO2011063937A1/en active Application Filing
- 2010-11-24 BR BR112012012506-0A patent/BR112012012506B1/en not_active IP Right Cessation
- 2010-11-24 EP EP10784453.2A patent/EP2504325B1/en not_active Not-in-force
- 2010-11-24 US US13/512,167 patent/US8735613B2/en not_active Expired - Fee Related
- 2010-11-24 KR KR1020127016479A patent/KR101420948B1/en active IP Right Grant
- 2010-11-24 CN CN201080053349.1A patent/CN102858758B/en not_active Expired - Fee Related
- 2010-11-26 TW TW099141074A patent/TWI430840B/en not_active IP Right Cessation
Patent Citations (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5329024A (en) | 1993-03-30 | 1994-07-12 | National Starch And Chemical Investment Holding Corporation | Epoxidation of olefins via certain manganese complexes |
EP0618202A1 (en) | 1993-03-30 | 1994-10-05 | National Starch and Chemical Investment Holding Corporation | Epoxidation of olefins via certain manganese complexes |
US20020004606A1 (en) | 1999-09-18 | 2002-01-10 | Georg Thiele | Process for the preparation of epoxides from olefins |
WO2005000827A1 (en) | 2003-06-18 | 2005-01-06 | Degussa Ag | Process for the epoxidation of propene |
WO2005095370A1 (en) | 2004-03-31 | 2005-10-13 | Council Of Scientific & Industrial Research | An improved catalytic process for the preparation of epoxides from alkenes |
EP2149569A1 (en) | 2008-08-01 | 2010-02-03 | Hexion Specialty Chemicals Research Belgium S.A. | Process for the manufacture of a 1,2-Epoxide |
Non-Patent Citations (5)
Title |
---|
DE VOS D E ET AL: "Epoxidation of terminal or electron-deficient olefins with H2O2, catalysed by Mn-trimethyltriazacyclonane complexes in the presence of an oxalate buffer", TETRAHEDRON LETTERS 19980514 GB, vol. 39, no. 20, 14 May 1998 (1998-05-14), pages 3221 - 3224, XP004116236, ISSN: 0040-4039 * |
DE VOS, TETRAHEDRON LETTERS, vol. 39, 1998, pages 3221 |
DIRK DE VOS ET AL.: "Epoxidation of Terminal or Electron- deficient Olefins with H202 catalysed by Mn-trimethyltriazacyclononane Complexes in the Presence of an Oxalate Buffer", TETRAHEDRON LETTERS, vol. 39, 1998, pages 3221 - 3224, XP004116236, DOI: doi:10.1016/S0040-4039(98)00205-6 |
ORGANIC SYNTHESIS, COLL., vol. 7, 1990, pages 126 |
SHUL'PIN ET AL.: "Oxidations by the system "hydrogen peroxide - [Mn2L203](PF6)2 (L=1,4,7-trimethyl-1,4,7-triazacyclononane)-oxalic acid". Part 6. Oxidation of methane and other alkanes and olefins in water", JOURNAL OF ORGANOMETALLIC CHEMISTRY, vol. 690, 2005, pages 4498, XP005097743, DOI: doi:10.1016/j.jorganchem.2005.01.065 |
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BR112012012506A2 (en) | 2015-09-08 |
US8735613B2 (en) | 2014-05-27 |
KR101420948B1 (en) | 2014-07-17 |
CN102858758A (en) | 2013-01-02 |
MY157588A (en) | 2016-06-30 |
TWI430840B (en) | 2014-03-21 |
AU2010324184B2 (en) | 2013-11-21 |
BR112012012506B1 (en) | 2017-12-26 |
EP2504325A1 (en) | 2012-10-03 |
EP2504325B1 (en) | 2017-06-14 |
RU2528385C2 (en) | 2014-09-20 |
EP2343288A1 (en) | 2011-07-13 |
CN102858758B (en) | 2016-01-20 |
US20120289722A1 (en) | 2012-11-15 |
JP5558578B2 (en) | 2014-07-23 |
RU2012126638A (en) | 2014-01-10 |
ES2634528T3 (en) | 2017-09-28 |
AU2010324184A1 (en) | 2012-06-14 |
KR20120106777A (en) | 2012-09-26 |
HUE034449T2 (en) | 2018-02-28 |
TW201132411A (en) | 2011-10-01 |
JP2013512205A (en) | 2013-04-11 |
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