51 results about "Propylbenzene" patented technology

The invention relates to a method for the increase production of BTX aromatic hydrocarbons and trimethylbenzene through hydrocracking heavy aromatic hydrocarbons to mainly solve technical problems of low heavy aromatic hydrocarbon added value and high cost for separating and producing trimethylbenzene monomers in the heavy aromatic hydrocarbons containing methylethylbenzene, propylbenzene and butylbenzene. The method comprises a step that the heavy aromatic hydrocarbons are subjected to a hydrocracking reaction through adopting Pt/Pd-loaded hydrogen type binder-free ten-membered ring zeolite as a catalyst under reaction conditions comprising that the reaction temperature is 320-450DEG C, the reaction pressure is 2.0-4.0Mpa, the hydrocarbons raw material weight hourly space velocity is 1.0-4.0h<-1> and the hydrogen/hydrocarbon raw material ratio by mole is 3-10:1. The method well solves the problems through above technical scheme, and can be applied to the industrial production of the BTX aromatic hydrocarbons and the trimethylbenzene.

The invention discloses propyl benzene latex with fine grain diameter for coating paper surface paint and a preparation method and application thereof. The latex is prepared by taking the following components as the raw materials in parts by weight in the mode of emulsion polymerization: 4-15 parts of seed emulsion, 100 parts of mixed monomer, 0.7-4.5 parts of emulsifier, 0.4-4.5 parts of initiator, 2-4 parts of accelerator, 2-8 parts of cross linking monomer, 4-20 parts of aqueous alkali and 90-290 parts of water, wherein the mixed monomer is composed of the following monomers in parts by weight: 20-44 parts of metacrylic acid ester, 50-74 parts of alpha methyl styrene and 6-10 parts of methacrylic acid. The propyl benzene latex with fine grain diameter for coating paper surface paint of the invention is an environmental-friendly high-property product which can be used by paper making paint. The product is applied in coating paper surface paint, can obviously strengthen the surface strength of the coating surface and improves paper coating glossiness.

The invention discloses a method for separating a mixture of m-ethyltoluene and p-ethyltoluene from C9 aromatics. The method comprises the following steps of: (1) mixing a C9 aromatics mixture and an accelerator, and sending into a heavy component eliminating tower, introducing a light component from the top of the tower, introducing a heavy component from a tower kettle; wherein the weight ratio of the C9 aromatics mixture to the accelerator is 1:0.05-0.5; (2) sending the light component from the step (1) into a light component eliminating tower, introducing the mixture of m-ethyltoluene and p-ethyltoluene from the tower kettle; (3) sending material flow introduced from the light component eliminating tower in the step (2) to an accelerator removal tower, introducing the accelerator from the tower top, introducing the material flow containing normal propylbenzene and isopropylbenzene from the tower kettle. The accelerator is acetonitrile and propionitrile. The mixture of m-ethyltoluene and p-ethyltoluene obtained by the method of the invention has the advantages of high purity, high yield and obvious separation effect.

Disclosed is nano anti-mildew energy-saving wall material, containing organic solvent, water, bentonite, diatomite, inorganic dye and filler, and addition agent. The organic solvent is one or more from polyvinyl alcohol, propyl benzene, propyl alcohol, ethylene glycol, alcohol ester and organic silicon resin; the bentonite is ca-bentonite; the inorganic dye and filler is one or more from titanium dioxide, talcum powder, light calcium carbonate, lithopone, wollastonite powder and wollastonite. The nano anti-mildew energy-saving wall material has the functions of absorbing and releasing moisture, adjusting room temperature, resisting mildew and bacteria, absorbing osmyl, noise and harmful substances, insulating and preserving heat, and resisting water and fire, and has water resistance and adhesive force, so the nano anti-mildew energy-saving wall material is a new environment-friendly paint better than latex paint.

A catalyst for synthesizing isopropylbenzene with low reaction temp (120-170 deg.C) and benzene/hydrocarbon ratio (2-5) and high stability is a modified molecular sieve.

A catalyst for the alkylation reaction of aromatic hydrocarbon and light alkane contains Mo element and ZSM-5 molecular sieve, wherein the weight ratio of the Mo element and the ZSM-5 molecular sieve is 1-16%. A binder of 5-40 wt% is added into the catalyst. In accordance with the embodiment of the catalyst in the alkylation reaction of aromatic hydrocarbon and light alkane, the reaction temperature is 250-450 DEG C, the material molar ratio of the aromatic hydrocarbon and light alkane is 0.5-3, the weight space-velocity is 0.2-5 h<-1>, accordingly, toluene, ethyl benzene, isopropyl benzene and n-propylbenzene can be prepared with high selectivity.

The invention relates to a trimethylbenzene separation method to mainly solve technical problems of long flow and high cost of previous separation of trimethylbenzene monomers from a heavy aromatic hydrocarbon material containing propylbenzene, methylethylbenzene and butylbenzene. The method, which adopts a technical scheme that the heavy aromatic hydrocarbon material which is C9 aromatic hydrocarbons with the content of aromatic hydrocarbons except trimethylbenzene being less than 0.5% sequentially enters a 1,3,5-trimethylbenzene tower and a 1,2,4-trimethylbenzene tower for being rectified and separated to obtain 1,3,5-trimethylbenzene products and 1,2,4-trimethylbenzene products, well solves the problems, and can be applied to the industrial production of trimethylbenzene.

The invention provides a method and an intermediate for synthesizing Fingolimod hydrochloride. The method comprises the following steps: performing nitro-substitution, formaldehyde condensation, reduction and salification on octyl halogenated propylbenzene by using a novel intermediate, thereby obtaining the Fingolimod hydrochloride. The synthetic method is short in route, high in yield, low in cost, mild in reaction conditions, simple and convenient in operation and high in product purity and has high application value in large-scale industrial production.

The invention discloses an anti-corrosion coating capable of emitting aromatic odor for a glass door. The anti-corrosion coating is characterized by being prepared from the following raw materials in parts by weight: 46-52 parts of a transparent polyurethane emulsion, 1-2 parts of a polyethylene wax emulsion, 20-24 parts of a modified styrene-acrylic emulsion, 1-3 parts of methoxy-1-methylethylacetate, 0.2-0.5 part of propanediol butyl ether bi(2-octyloxy pyrophosphate-yl) ethylene titanate, 0.2-0.4 part of a polyacrylate flatting agent, 1-2 parts of ethyl acetate, 0.2-0.3 part of ethyecellulose, 0.2-0.5 part of polyether-modified polyethylene organic siloxane, 0.3-0.6 part of propyl triethoxy siloxane, 0.3-0.7 part of menthyl acetate, 0.2-0.5 part of polyoxyethylene oleate, 0.3-0.5 part of phenoxyaethanol, 1-3 parts of a pigment, 1-2 parts of nano ceramic powder and 10-15 parts of deionized water. The water-based coating disclosed by the invention has excellent water resistance, rot resistance and adhesive force, also has fresh aromatic odor, and is refreshing; the coating has the effects of sterilizing, preventing dust, resisting static electricity and the like due to the added modified styrene-acrylic emulsion; and the quality of the coating is further improved.

The invention relates to elastic thermal insulation slurry and a preparation method thereof. The elastic thermal insulation slurry is prepared from the following raw materials in percentage by weight:8-12% of polymer emulsion, 10-12% of silica powder, 12-18% of coarse whiting powder, 25-30% of glass micro-beads, 6-8% of calcined kaolin, 4-5% of barium sulfate, 1-1.5% of a flame retardant, 0.2-0.5% of a wetting agent and the balance of water. According to the invention, the silica powder is used as a light skeleton, the polymer emulsion and the calcined kaolin are added at the same time, so that the binding power of slurry is improved, the slurry can be quickly coagulated, strong binding strength with a base material is generated and is up to 0.11 MPa, the cured propylbenzene emulsion is high in strength, good toughness of the product can be guaranteed, and after being mounted on a wall, the elastic thermal insulation slurry is not easy to crack and fall off; and the slurry is good inheat preservation performance, the vitrified micro bubbles are added, so that the heat conductivity coefficient of the obtained slurry is smaller than 0.053 W/(m.K), and the slurry has good flame retardance.

Methods and apparatuses are provided for producing xylene. A method includes combining a propylbenzene containing feed with a xylene raffinate stream, where the xylene raffinate stream is provided from a xylene recovery unit. The xylene raffinate stream and the propylbenzene containing feed are isomerized in an isomerization unit to produce an xylene isomerization effluent stream, where the xylene isomerization effluent stream includes aromatic compounds having 8, 9, or 10 carbons atoms. The aromatic compounds having 8 carbon atoms are separated from the aromatic compounds having 9 or 10 carbons, and the aromatic compounds having 8 carbons are fed to the xylene recovery unit. The aromatic compounds having 9 or 10 carbons are transalkylated with toluene to produce xylene.

The invention discloses an anticorrosive anti-yellowing coating for a glass door. The coating is characterized by being prepared from the following raw materials in parts by weight: 8 to 12 parts of water-based vinyl polyurethane, 30 to 35 parts of amino resin emulsion, 0.1 to 0.3 part of water-based silane coupling agent KH460, 26 to 32 parts of modified styrene-acrylic emulsion, 1 to 3 parts of dipropylene glycol dimethyl ether, 0.3 to 0.5 part of alcohol amine alkoxy titanate ester, 0.2 to 0.4 part of fluoro-alkyl polyether modified polysiloxane, 0.1 to 0.3 part of lauroyl diethanolamide, 0.2 to 0.3 part of white oil, 0.2 to 0.4 part of polyoxyethylene sorbitan monooleate, 0.1 to 0.2 part of ammonium polyphosphate, 0.3 to 0.7 part of ethylparaben, 0.2 to 0.5 part of glycerin, 0.3 to 0.6 part of quartz powder, 1 to 3 parts of pigment and 10 to 15 parts of deionized water. The sterilization, the dust prevention, the anti-static performance and the like of the coating are improved due to the added modified styrene-acrylic emulsion; the coating has the functions of sterilization and anticorrosion due to the added ethylparaben; and on the basis of water resistance, acid resistance and an excellent adhesive force of the water-based coating, the water-based coating is also good in weatherability, aging resistance and anticorrosion.

The invention belongs to the field of petrochemical industry and discloses a separation process for producing an ethylbenzene and/or propylbenzene product from gas containing ethylene and/or propylene by a gas phase process. The separation process comprises the following steps: 1) feeding alkylation reaction products getting out of an alkylation reactor and anti-alkylation reaction products getting out of an anti-alkylation reactor into a benzene tower respectively or after mixing; 2) feeding gas-phase materials at the top of the benzene tower after separation into an absorption tower after the gas-phase materials are drawn out of the tower top of the benzene tower; 3) drawing out liquid-phase materials at the upper part of the benzene tower after separation from the tower top or the side of the benzene tower and then returning the liquid-phase materials into the reaction part; and 4) performing corresponding separation on the materials at the tower bottom of the benzene tower by a subsequent separation tower to obtain several or all of methylbenzene, ethylbenzene, propylbenzene, diethylbenzene and high-boiling residues. By adopting the separation process disclosed by the invention, by directly bringing heat of the reaction products, including reaction heat, into the benzene tower, the heat supply at the tower bottom of the benzene tower is reduced and the energy consumption is reduced; and the utilization of the heat is reasonable. By adopting the separation process disclosed by the invention, the number of the towers required for separation is not increased, and indirect heat exchange equipment is reduced.

The present invention provides a method for preparing high-purity trans-1-(2,2-difluoro-4-propylcyclohexyl)-4-propylbenzene at a high yield. The method comprises the following steps: a Lewis acid is used to catalyze a chiral isomerization reaction of a mixture formula 3 to obtain high-purity (trans:cis > 90:10) trans-2-(4-propylphenyl)-5-propylcyclohexanone (formula 2); and the high-purity (trans:cis > 90:10) trans-2-(4-propylphenyl)-5-propylcyclohexanone (formula 2) undergoes a fluorination reaction to prepare the high-purity trans-1-(2,2-difluoro-4-propylcyclohexyl)-4-propylbenzene (formula1). The method has the advantages of high yield, easiness in separation and purification of the product, few wastes, low cost and easiness in industrialization.

An auxiliary paint for steel rings of automobile wheels, relating to the technical field of automobile wheel processing and production, characterized in that: it is made of the following materials in parts by weight: 11-17 parts of resin, 6-10 parts of phenol, diisoperoxide 4-9 parts of propylene, 125-10 parts of nylon, 4-9 parts of accelerator DM, 1-5 parts of polyester acrylate, 1-3 parts of triethanolamine, 6-12 parts of modified fluorite, 1-6 parts of bamboo charcoal , 5‑10 parts of hexamethylenetetramine, 2‑8 parts of tetramethoxymethyl glycoluril, 8‑15 parts of defoamer, 8‑15 parts of antiaging agent, 5‑10 parts of biomass auxiliary materials, deionized 20‑27 parts of water. The invention has the advantages of reasonable method, convenient operation, high strength and corrosion resistance.

The invention provides a synthesizing method of a propiophenone compound, and belongs to the technical field of organic synthesizing. The synthesizing method has the advantages that the reaction steps for synthesizing the propiophenone compound can be simplified, and the reaction cost is reduced. The synthesizing method of the propiophenone compound comprises the following steps of adding propylbenzene, organic acid, iodine and tert-butyl hydroperoxide into a reaction kettle, and reacting for 8-24h at the temperature of 80-120 DEG C; after the reaction is finished, extracting a reaction solution by an organic solvent, and drying, so as to obtain the propiophenone compound. The synthesizing method can be used for the synthesizing and preparation of the propiophenone compound.

The preparation method of the catalyst comprises the following steps: mixing at least one zeolite with a binder, adding water and a peptizing agent, kneading, extruding and molding, and then sequentially drying and roasting, finally, the roasted catalyst is subjected to metal or nonmetal oxide modification through an impregnation method, and the required catalyst is obtained. According to the present invention, benzene and C4 olefin are adopted as reaction raw materials, the catalyst obtained by using the preparation method is adopted to catalyze the reaction of benzene and butene so as to generate the target product mixed propylbenzene, the reaction can be performed under the mild reaction condition, the reaction speed is high, and the olefin conversion rate is high. Through measurement, under the conditions that the reaction temperature is 360 DEG C, the reaction pressure is 0.8 MPa, the total weight hourly space velocity is 5.0 h <-1 > and the molar ratio of benzene to alkene is 5.5: 1, the conversion rate of C4 olefin reaches 99.8%, the selectivity of the product mixed propylbenzene reaches 72.6%, the proportion of isopropyl benzene in the mixed propylbenzene is 52.69%, and the proportion of n-propylbenzene in the mixed propylbenzene is 47.31%.

The invention discloses a bonded three-dimensional covalent organic framework chromatographic column and separation application thereof. An aromatic structure three-dimensional covalent organic framework JNU-5 with high thermal stability and rich amino groups is prepared as a gas chromatography stationary phase, a JNU-5 covalent bonded capillary column is further prepared through an in-situ growth method, and high-performance gas chromatography separation of xylene, dichlorobenzene, propylbenzene and other isomers is successfully achieved. Besides the isomeride, the prepared JNU-5 covalent bonding capillary column also has a good separation effect on common substances such as n-alkanes, benzene homologues, normal alcohols and the like, and the chromatographic column can be repeatedly used for multiple times. The invention not only provides a preparation method of the bonded three-dimensional covalent organic framework-based capillary gas chromatographic column, but also provides a new solution for efficient separation of isomeride.