36 results about "Ethylbenzene hydroperoxide" patented technology

A titanium-containing silicon oxide catalyst satisfying all of the following conditions (1) to (4):(1): an average pore size of 10 Å or more,(2): a pore size of 90% or more of the total pore volume of 5 to 200 Å,(3): a specific pore volume of 0.2 cm3/g or more, and(4): a quarternary ammonium ion represented by the following general formula (I) is used as a template and then said template is removed by solvent extraction operation;wherein, R1 represents a linear or branched hydrocarbon chain having 2 to 36 carbon atoms, and R2 to R4 represent an alkyl group having 1 to 6 carbon atoms, a method for producing said catalyst, and a method for producing propylene oxide by reacting propylene with a hydroperoxide, except for ethylbenzene hydroperoxide, in the presence of said catalyst.

A method for producing propylene oxide by reacting propylene with ethylbenzene hydroperoxide, wherein the reaction is conducted in the presence of a catalyst comprising a titanium-containing silicon oxide and satisfying all of the following conditions (1) to (6):(1) there is at least one peak showing a interplanar spacing (d) larger than 18 Å in X-ray diffraction;(2) an average pore size is 10 Å or more;(3) a pore size of 90% or more of the total pore volume is 5 to 200 Å;(4) a specific pore volume is 0.2 cm3/g or more;(5) a quaternary ammonium ion represented by the following general formula (I) is used as a template and then said template is removed by calcination operation:wherein R1 represents a linear or branched hydrocarbon chain having 2 to 36 carbon atoms, and R2 to R4 represent an alkyl group having 1 to 6 carbon atoms; and(6) The catalyst has been subjected to silylation treatment.

A process for producing propylene oxide by reacting propylene with ethylbenzene hydroperoxide in the presence of a titanium-containing silicon oxide catalyst satisfying all of the following conditions (1) to (4): (1): an average pore size of 10 ANGSTROM or more, (2): a pore size of 90% or more of the total pore volume of 5 to 200 ANGSTROM , (3): a specific pore volume of 0.2 cm3/g or more, and (4): a quarternary ammonium ion represented by the following general formula (I) is used as a template and then said template is removed by solvent extraction operation;[NR1R2R3R4]+(I) wherein, R1 represents a linear or branched hydrocarbon chain having 2 to 36 carbon atoms, and R2 to R4 represent an alkyl group having 1 to 6 carbon atoms.

The invention discloses a method for preparing an ethylbenzene hydroperoxide through oxidation of ethylbenzene. A multistage oxidation reactor is adopted. A liquid-phase ethylbenzene reactor flows into the multistage oxidation reactor step by step for gradual oxidation to produce an oxidized mixture containing ethylbenzene hydroperoxide. An oxygen-containing gas is blown into the multistage oxidation and taken as an oxidant. Through optimized multistage reaction technology, the problem of a horizontal reactor in the prior art can be overcome, backmixing of a liquid phase is improved, selectivity of the ethylbenzene hydroperoxide which is a target product is improved, and the oxidation efficiency of ethylbenzene is increased. The security and stability of an oxidation reaction of liquid ethylbenzene in an actual operation are ensured, and the economic benefit of the apparatus is maximized.

The invention relates to an epoxybutane production method to mainly solve the problems of large amount of wastewater and waste residues, severe pollution and strong apparatus corrosion existing in the prior art. The method comprises the following steps: 1, carrying out a peroxidation reaction on ethylbenzene and air to obtain an ethylbenzene hydroperoxide oxidation solution; 2, carrying out an epoxidation reaction on the ethylbenzene hydroperoxide oxidation solution and butylene under the action of a catalyst under liquid phase conditions to generate epoxybutane, alpha-methylbenzyl alcohol and acetophenone; 3, dehydrating alpha-methylbenzyl alcohol to generate styrene; and 4, carrying out a hydrogenation reaction on acetophenone and hydrogen to generate alpha-methylbenzylalcohol, returning the generated alpha-methylbenzylalcohol to step 3, and hydrogenating the returned alpha-methylbenzylalcohol and the alpha-methylbenzylalcohol generated in step 2 to generate styrene. The method adopting the above technical scheme well solves the problems, can be used in industrial production for preparation of epoxybutane and combined production of styrene.

The invention relates to a method for preparing ethylbenzene hydroperoxide by virtue of an ethylbenzene liquid phase and a preparation method of epoxypropane. According to the method, by adding a small amount of organic alkali substances, the peroxidation reaction between ethylbenzene gas containing oxygen molecules is promoted. According to the method, the selectivity of a target product can be effectively improved, and the activity of a subsequent epoxidation catalyst is not influenced by the added organic alkali substances.

The invention relates to a production method for epichlorohydrin. The method mainly solves the problems of large amounts of waste water and waste residues, serious pollution and strong corrosiveness to equipment in the prior art. A technical scheme of the invention adopts the production method which comprises the following steps: with chloropropene and ethylbenzene hydroperoxide as raw materials and ethylbenzene as a solvent, subjecting the raw materials and a titanium-contained porous silicon dioxide catalyst to contact reaction so as to obtain epichlorohydrin and alpha-methylbenzyl alcohol under the conditions that reaction temperature is 25 to 200 DEG C; reaction absolute pressure is 0.1 to 8.0 MPa; a molar ratio of chloropropene to ethylbenzene hydroperoxide is 1 to 15; and weight-space velocity of ethylbenzene hydroperoxide is 0.01 to 20 h<-1>. Thus, the problem is well solved, and the method can be applied in industrial production of epichlorohydrin.

Oxidative desulfurization (ODS) is an attractive alternative to hydrodesulfurization (HDS) technology due to its lower energy requirement for the removal of refractory sulfur species, such as dibenzothiophene (DBT), from heavier petroleum streams. Diesel containing DBT may be oxidized using a heterogeneous titanium(IV) catalyst and organohydroperoxide oxidant, such as tert-butyl hydroperoxide (TBHP), cumyl hydroperoxide (CHP) and/or ethylbenzene hydroperoxide (EBHP), which proves effective for the selective oxidation and removal of refractory sulfur compounds from diesel fuel.

The invention relates to a method for preparing epoxy propane from ethylbenzene hydroperoxide and propylene, and is used for mainly solving the problems in the prior art that reaction temperature rising is higher and higher molar ratio of propylene to ethylbenzene hydroperoxide is needed for maintaining higher reaction efficiency. The problems are better solved through adopting the technical schemes that raw materials of ethylbenzene hydroperoxide and liquid propylene go into a multistage adiabatic reactor, and under conditions of the reaction temperature of 15-160 DEG C, the pressure of 1.0-12.0 MPa and the total molar ratio of propylene to ethylbenzene hydroperoxide of 1-20, the raw materials make contact with a Ti-silica catalyst and subjected to an epoxidation reaction to generate epoxy propane, wherein the raw material ethylbenzene hydroperoxide goes into catalyst bed layers of the multistage adiabatic reactor in a sectionalized manner, and a part of epoxidation reaction products containing epoxy propane circulate to an inlet of the reactor. The method can be used in industrial production of preparation of epoxy propane through epoxidation of ethylbenzene hydroperoxide and propylene.

The invention relates to an epoxidation cyclic process for preparing epoxy propane from ethylbenzene hydroperoxide and propylene, and is used for mainly solving the problems in the prior art that reaction temperature rising is higher and higher molar ratio of propylene to ethylbenzene hydroperoxide is needed for maintaining higher reaction efficiency. The problems are better solved through adopting the technical schemes that a raw material ethylbenzene hydroperoxide sectionally goes into at least two series-connection adiabatic reactors and a raw material liquid propylene goes into at least two series-connection adiabatic reactors, and under conditions of the reaction temperature of 15-160 DEG C, the pressure of 1.0-12.0 MPa and the total molar ratio of propylene to ethylbenzene hydroperoxide of 1-20, the raw materials make contact with a Ti-silica catalyst and subjected to an epoxidation reaction to generate epoxy propane, wherein a part of epoxidation reaction products containing epoxy propane circulate to catalyst bed layers of the reactors. The method can be used in industrial production of preparation of epoxy propane through epoxidation of ethylbenzene hydroperoxide and propylene.

The invention relates to a method for preparing epoxy propane through epoxidation of ethylbenzene hydroperoxide and propylene, and is used for mainly solving the problems in the prior art that reaction temperature rising is higher and higher molar ratio of propylene to ethylbenzene hydroperoxide is needed for maintaining higher reaction efficiency. The problems are better solved through adopting the technical schemes that raw materials of ethylbenzene hydroperoxide and liquid propylene go into a multistage adiabatic reactor, and under conditions of the reaction temperature of 15-160 DEG C, the pressure of 1.0-12.0 MPa and the total molar ratio of propylene to ethylbenzene hydroperoxide of 1-20, the raw materials make contact with a Ti-silica catalyst and subjected to an epoxidation reaction to generate epoxy propane, wherein all or a part of the raw material propylene goes into an inlet of the multistage reactor, and the raw material ethylbenzene hydroperoxide sectionally goes into catalyst bed layers of the multistage adiabatic reactor in a sectionalized manner. The method can be used in industrial production of preparation of epoxy propane through epoxidation of ethylbenzene hydroperoxide and propylene.

The invention discloses a device and method for oxidizing organic matters, particularly a method for preparing ethylbenzene hydroperoxide by reacting ethylbenzene with an oxygen-containing gas. The device includes a vertical bubbling reactor and a horizontal bubbling reactor connected to a reaction product outlet of the vertical bubbling reactor. The horizontal bubbling reactor is provided with aplurality of reaction compartments arranged along the axial direction inside, with a liquid phase passage being between adjacent reaction compartments. Through ingenious combination of the reactors, organic matter oxidation can be performed under more favorable conditions, thereby improving the production capacity of the device.

The invention relates to a method for preparing an efficient titanium silicalite molecular sieve catalyst. The method comprises the following steps: mixing and hydrolyzing a mixture composed of a silicon source, a template agent, a mineralizer, water and ethanol according to a volume ratio of 1:1 at normal temperature; slowly adding a mixture of a titanium source and the residual silicon source into the hydrolyzed silicon hydroxide solution while rapidly stirring, and forming gel; transferring the gel into a crystallization kettle for crystallizing; washing, filtering and roasting a crystallized molecular sieve so as to remove the template agent, wherein the calcination temperature is 500-600 DEG C, and the calcination time is 4-6 hours, thereby obtaining the composite porous molecular sieve based catalyst. The catalyst is simple in preparation process and high in production efficiency; moreover, because the molecular sieve structure contains organic functional groups and composite pores with hydrophobic property and carbon deposition resistance, the catalyst is excellent in hydrophobic property and mass transfer performance and high in activity, selectivity and stability, and can be used in the process of producing corresponding epoxides through olefin epoxidation by taking H2O2, ethylbenzene hydroperoxide, isopropylbenzene hydroperoxide, tert-butyl hydroperoxide and the like as oxidizing agents.

The invention discloses a method for improving the stability of ethylbenzene hydroperoxide. The method includes the step of addition of malonic acid derivatives and/or succinic acid derivatives duringthe preparation of ethylbenzene hydroperoxide. The method can effectively inhibit decomposition of ethylbenzene hydroperoxide produced by oxidation, is especially suitable for an SMPO process, and isbeneficial to improvement of the stability of the intermediate ethylbenzene hydroperoxide in the process. The method cannot introduce metal cationic sodium or potassium and the like, can reduce scaling problems caused by material entrainment and the like, reduces discharge of phosphorus-containing wastewater, has good environmental protection, and improves the selectivity and yield of the reaction.

The invention relates to a process for the liquid phase oxidation of ethylbenzene into ethylbenzene hydroperoxide, wherein the ethylbenzene hydroperoxide concentration is kept below 20 wt. % on the basis of the total weight of the reaction mixture, and wherein styrene and/or a styrene derivative is fed to the ethylbenzene. The concentration of said styrene and/or a styrene derivative may be from 0.01 to 5.0 wt. %.

The invention relates to application of a titanium silicalite molecular sieve catalyst. The catalyst is used in the process of producing corresponding epoxides through olefin epoxidation by taking H2O2, ethylbenzene hydroperoxide, isopropylbenzene hydroperoxide, tert-butyl hydroperoxide and the like as oxidizing agents. The catalyst is composed of a silicon source, a titanium source, a template agent, a mineralizer and a solvent, wherein the silicon source is Si(OR1)4, (R2O)3Si-(CH2)n1-Si(OR3)3 and (R4)n2-Si(OR5)4-n2; the titanium source is Ti(OR6)4; the template agent is [(CH3)3CH3(CH2)n3N<+>]X<->; the mineralizer is [(CH3Cn4H2n4)4NH4]<+>OH<->; the solvent is water. Moreover, because the molecular sieve structure contains organic functional groups and composite pores with hydrophobic property and carbon deposition resistance, the catalyst is excellent in hydrophobic property and mass transfer performance and high in activity, selectivity and stability.

The invention relates to a method for preparing a molecular sieve based catalyst. The method comprises the following steps: mixing and hydrolyzing a silicon source, a template agent, a mineralizer, water and ethanol at normal temperature; slowly adding a mixture of a titanium source and the residual silicon source into the hydrolyzed silicon hydroxide solution under rapid stirring, and forming gel; transferring the gel into a crystallization kettle for crystallization; washing, filtering and roasting a crystallized molecular sieve so as to remove the template agent, wherein the calcination temperature is 500-600 DEG C, and the calcination time is 4-6 hours to obtain the composite porous molecular sieve based catalyst. The catalyst is simple in preparation process and high in production efficiency; and moreover, because the molecular sieve structure contains organic functional groups and composite pores with hydrophobic property and carbon deposition resistance, the catalyst is excellent in hydrophobic property and mass transfer performance and high in activity, selectivity and stability, and can be used in the process of producing corresponding epoxides through olefin epoxidation by taking H2O2, ethylbenzene hydroperoxide, isopropylbenzene hydroperoxide, tert-butyl hydroperoxide and the like as oxidizing agents.

The invention discloses a method for preparing ethylbenzene hydroperoxide through ethylbenzene reactive distillation and a reactive distillation tower thereof. A catalyst bag is fixed between gas raising covers of a tower plate, and the catalyst bag further comprises a strip-shaped catalyst. The method is high in efficiency, raw materials pass through the catalyst and the tower plate separation and purification element repeatedly, and the conversion rate and selectivity are improved. Meanwhile, the manufacturing is easy, the mounting and dismounting are convenient, and follow-up treatment is simplified.