34 results about "Benzene vapor" patented technology

The present invention relates to a refining system of coked crude benzole and a refining method thereof. The basic equipment consists of two benzene towers, a primary tower, a first pure benzene tower, a second pure benzene tower, a toluene tower and a xylene tower. The heat of the reboiler of the primary tower comes from toluene vapor on the top of the toluene tower; the heat of the reboiler of the first pure benzene tower comes from the pure benzene vapor on the top of the second pure benzene tower. The refining method comprises pre-distillation, refining of the pure benzene and separation of the toluene and the xylene. The method not only saves energy but also reduces the cost of investment. The process is simplified. Compared with the traditional sulfuric acid washing process, the method eliminates the acid-alkali washing and benzene blowing processes. The whole process generates no waste acid, acid residue, caustic dross or waste water, which can cause serious damage to the environment. Compared with the catalytic hydrogenation, the method has the advantages of simplifying the process, lowering the energy consumption, reducing the cost of investment and production, and improving the benefit of production, and thus being an excellent method for steel enterprises and coking enterprises to further process and make use of by-products.

The invention relates to a catalyst for the preparation of ethylbenzene by ethanol and benzene vapor-phase alkylation and mainly solves the problem that the content of xylene impurity in the product ethylbenzene is high and a catalyst has poor stability and short regeneration period in the prior art. The catalyst provided by the invention comprises the following ingredients: by weight, a) 40-90% of a ZSM-5 molecular sieve with the silicon-aluminium mol ratio SiO2/Al2O3 being 30-400 and grain size being 5-350 nm; b) 9-59% of a binder alumina or silicon dioxide; and c) 0.1-10% of alkaline earth oxide. By the adoption of the technical scheme, the above problem is well solved. The catalyst can be used in the industrial production of ethylbenzene prepared by ethanol and benzene vapor-phase alkylation.

The invention relates to an activated carbon desorption method of an activated carbon canister in a benzene vapor recovery device. The method mainly solves the problem that activated carbon is prone to desorption at low temperature in the prior art. According to the technical scheme, the activated carbon desorption method comprises the steps that after adsorption of the activated carbon canister in the benzene vapor recovery device is saturate, an activated carbon bed layer is regenerated on the vacuum condition; after the pressure in the activated carbon canister is reduced to 5.0 kPa, air is blown into a heat exchanger to exchange heat with vapor to reach 40-60 DEG C and then enters the activated carbon bed layer in the activated carbon canister for replacement, and more benzene molecules are desorbed from the activated carbon bed layer and enter the follow-up treating process through a vacuum pump and a compressor. The activated carbon desorption method can be used for desorption of the activated carbon canister in the benzene vapor recovery device.

The invention discloses a benzene organic vapor recycling device and a benzene organic vapor recycling method. The benzene organic vapor recycling device comprises a low-temperature condensing device, a variable-temperature adsorbing device and a variable-pressure adsorbing device, wherein the low-temperature condensing device comprises a cold-box heat exchanger, a refrigerating compressor and a condensing heat exchanger which are sequentially connected; a vapor inlet of the cold-box heat exchanger is connected with a benzene organic vapor outlet; the condensing heat exchanger is connected with the cold-box heat exchanger through a valve to form a cooling circulating system; the condensing heat exchanger is further provided with a cooling water inlet and a cooling water outlet to form a water circulating system; the cold-box heat exchanger is further provided with a liquid outlet; the liquid outlet of the cold-box heat exchanger is connected with a layering trough and is used for recycling benzene liquid. The benzene organic vapor recycling device recycles and purifies benzene vapor through the low-temperature condensing device, the variable-temperature adsorbing device and the variable-pressure adsorbing device; finally, the benzene organic vapor achieves a concentration lower than 12 mg/m<3> and completely reaches the discharge standard; no secondary pollution is generated during operation of the benzene organic vapor recycling device.

The invention relates to a method for preparing ethylbenzene by ethanol and benzene vapor-phase alkylation and mainly solves the problem that the content of xylene impurity in the product ethylbenzene is high and a catalyst has poor stability and short regeneration period in the prior art. According to the invention, ethanol and benzene are used as reaction raw materials. Under the condition that reaction temperature is 300-460 DEG C, reaction pressure is 0.5-2.8 MPa, ethanol WHSV is 0.1-5.0h<-1> and the benzene/ethanol mole ratio is 2-10, the reaction raw materials contact with a catalyst to carry out vapor-phase alkylation reaction so as to generate ethylbenzene. The catalyst used comprises the following ingredients of: by weight, a) 40-90% of ZSM-5 molecular sieve with the silicon-aluminium mol ratio SiO2/Al2O3 being 30-400 and grain size being 5-350 nm; b) 9-59% of a binder alumina or silicon dioxide; and c) 0.1-10% of alkaline earth oxide. The catalyst successively undergoes high-temperature stream and phosphoric acid treatments before used. By the adoption of the technical scheme, the above problem is solved well. The method provided by the invention can be used in industrial production of ethylbenzene prepared by ethanol and benzene vapor-phase alkylation.

The invention relates to a benzene recovery and treatment device and its treatment method. The treatment device mainly includes a condenser, an adsorption tank and an absorption tower, and has the advantages of novel design, reasonable structure and convenient use, combined with the "condensation + adsorption + absorption" The treatment method can have a significant effect on the recovery and treatment of benzene vapor.

The invention discloses a method for removing thiophenic sulfur from coking benzene, belonging to the field of chemical industry production of benzene. The method comprises the following steps: conveying fresh benzene to a benzene heat exchanger by a fresh benzene pump under the pressurizing action, exchanging heat, conveying to a benzene electric heater, mixing hydrogen gas with benzene steam, heating and gasifying, and conveying to a benzene desulfurization reactor; enabling the temperature to be 210-260 DEG C, the pressure to be 0.75-1.05MPa and the air velocity to be 2-3h<-1> in the benzene desulfurization reactor, adding thiophene with hydrogen to be converted into hydrogen sulfide under the action of a catalyst NHDS-8, and adsorbing onto the catalyst; enabling the benzene steam after desulfurization to enter into the benzene heat exchanger so as to convert gaseous benzene into liquid benzene; and carrying out gas-liquid separation on the liquid benzene and the hydrogen in a benzene separator, decompressing the liquid benzene through an adjusting valve, conveying to a benzene process tank, separating the hydrogen through a wire mesh demister, and conveying to a hydrogen circulator for further circulation. The method is better in thiophene removal performance, is capable of reducing the thiophene content in raw materials to be in PPb level, and is low in investment cost and simple to operate.

The invention discloses a preparation method of a hydroxy-functionalized carboxyl-terminated polybutadiene-acrylonitrile copolymer/carbon nanotube conducting composite film. The method comprises the following steps: carrying out in-situ coupling reaction on a hydroxy-functionalized carboxyl-terminated polybutadiene-acrylonitrile copolymer and uniform hydroxy multiwall carbon nanotubes subjected to ultrasonic dispersion to form a polyurethane compound by using hexamethylene diisocyanate, coating a film, and drying at room temperature to obtain the hydroxy-functionalized carboxyl-terminated polybutadiene-acrylonitrile copolymer/carbon nanotube conducting composite film. The method is simple to operate and easy for film formation, and has the advantages of low energy consumption, short operation time and favorable dispersibility of the carbon nanotubes; the obtained conducting composite film can implement detection on benzene and methylbenzene solvent vapor, has the advantages of short response time, high sensitivity and high selectivity, can not cause permanent damage to the conducting film, can implement the ppm-level detection on the benzene vapor, and can implement repeated use.

The invention discloses metal nanoparticle loaded activated carbon. According to the metal nanoparticle loaded active carbon, metal nanoparticle dispersion liquid and an activated carbon carrier are fully mixed and then are put into high-temperature airflow to be dried so as to obtain the metal nanoparticle loaded activated carbon, the loading capacity of metal nanoparticles is 2-14% of the mass of the activated carbon carrier, and the mass of the metal nanoparticle dispersion liquid is 48-70% of the mass of the activated carbon carrier. The invention further discloses related production equipment used for the metal nanoparticle loaded activated carbon and a preparation method for the metal nanoparticle loaded activated carbon. The metal nanoparticle loaded activated carbon obtained by utilizing the preparation method for the metal nanoparticle loaded activated carbon has the advantages that the particle size distribution of the loaded metal nanoparticles is uniform, the physical adsorption performance and the chemical catalytic performance of the activated carbon are balanced and efficient, a preparation process is simple, and non-polar harmful gas such as benzene vapor, chloroethane vapor and formaldehyde and strong-polarity harmful gas such as cyanogen chloride and hydrocyanic acid can be effectively adsorbed.

The invention provides a hierarchical pore carbon material as well as a preparation method and an application thereof, and belongs to the field of porous materials. The hierarchical porous carbon material provided by the invention comprises micropores, mesopores and macropores, chlorine ions are loaded on the outer surface of the hierarchical pore carbon material and the surfaces of pore channels,and the outer surface of the hierarchical pore carbon material and the surfaces of the pore channels further contain carbon-oxygen functional groups. The hierarchical pore carbon material provided bythe invention is used as an adsorbent and can adsorb mercury vapor, arsenic vapor, selenium vapor and volatile organic pollutants. The results of embodiments show that the hierarchical pore carbon material provided by the invention can effectively adsorb elemental mercury vapor, VOCs (represented by benzene vapor and o-xylene vapor), arsenic vapor and selenium vapor.

The invention discloses a test device for simulating protection time of a canister to benzene vapor and a use method. The test device comprises a box body, and the interior of the box body is divided into a benzene generation chamber, a constant-temperature chamber and a humidity generation chamber; the benzene generation chamber and the humidity generation chamber are both connected with the gas source interface; a reagent bottle and a heating system are arranged in the benzene generating chamber; a humidifying system is arranged in the humidity generating chamber; a mixing tank and a simulated canister are arranged in the constant-temperature chamber; and a human-computer interface and a switching power supply are arranged outside the constant-temperature chamber. The device can perform simulation test on benzene vapor protection time of different canister products, test the benzene vapor protection time of the canister under the conditions of different temperature and humidity, air inlet flow and concentration and different carbon layer thicknesses, does not need to use a canister finished product, saves research cost, is accurate and stable in test condition control, is integrally designed, the device can be integrally controlled, is simple to operate, and is suitable for scientific research on the protection time of the canister on the benzene vapor.

The invention relates to high-silicon mordenite and a preparation method thereof, and the preparation method comprises the following steps: step S1, treating Na-MOR with SAR = 14, which is hydrothermally synthesized in a fluorine-free all-inorganic silicon oxide-aluminum oxide-water reaction mixture system, with a sulfuric acid solution to prepare H-MOR zeolite; s2, carrying out high-temperature steam roasting on the H-MOR zeolite; step S3, carrying out acid solution treatment on the roasted H-MOR zeolite; and S4, washing the H-MOR zeolite treated by the acid solution, filtering, and drying to prepare the hydrophobic MOR zeolite. The high-silicon mordenite is hydrophobic MOR zeolite, the hydrophobic coefficient of the high-silicon mordenite is larger than 1, the benzene vapor adsorption capacity of the high-silicon mordenite is larger than 5.4%, the water vapor adsorption capacity of the high-silicon mordenite is smaller than 4.5%, the BET surface area of the high-silicon mordenite is larger than 530 m < 2 >/g, and the micropore volume of the high-silicon The hydrophobic MOR zeolite with the hydrophobic coefficient H larger than 1 is prepared through water vapor roasting and subsequent acid treatment modification, and the hydrophobic MOR zeolite has the good micropore adsorption property.

The invention belongs to the technical field of fishing gear processing, and in particular relates to a processing method of high-strength polyethylene twisted net sheet, which includes primary benzene steam setting, cooling and secondary hot steam setting. Compared with the prior art, the present invention has the following advantages: in the present invention, when the linear density is slightly increased by adding compounding additives to the high-strength polyethylene monofilament raw material, the tensile mechanical properties are also improved to a certain extent, and at the same time The woven mesh is stretched once and the benzene steam is set for the first time to modify the mesh, so that the spatial structure is more complex, the molecular structure is tighter, and the strength is increased; the mesh is stretched twice and the hot steam is set, reducing The retraction rate of the mesh is improved, and the product quality of the fishing net is guaranteed. Compared with the mesh of the same specification, the breaking strength is increased by about 3.5%, and the scope of application is wider.

The invention discloses a method for removing liquid-phase benzene retained in a catalyst of a liquid-phase ethylbenzene alkylation and transalkylation reactor through superheated benzene steam purging. The superheated benzene steam is used as a purging medium and can replace most of the existing steam purging methods for ethylbenzene production devices by a liquid phase method so that the servicelife of the catalyst of an ethylbenzene unit is prolonged, and the selectivity and the conversion rate of a regenerant are prevented from deteriorating; compared with a method for removing the liquid-phase benzene in the catalyst through hot nitrogen purging, the method is beneficial to reducing the equipment investment of a circulating nitrogen system and reducing the one-way purging consumptionof nitrogen, and the economic benefit is more outstanding.

The invention discloses a separation system for reducing vapor-liquid entrainment of a vapor phase pipe of a debenzolization tower. The separation system for reducing the vapor-liquid entrainment of the vapor phase pipe of the debenzolization tower comprises a liquid sealing pipe and a liquid sealing discharge pipe, wherein the liquid sealing pipe is formed by connecting three straight pipes and two U-shaped elbow pipes and arranged below a vapor phase inlet main pipe, and the bottom end of one lower elbow pipe and the vapor phase inlet main pipe are located on the same level line. An upper end opening of the liquid sealing pipe is connected with the lower end of a vertical pipe of the vapor phase inlet main pipe, and a lower end opening of the liquid sealing pipe is connected on a vapor phase outlet main pipe. The liquid sealing height of the liquid sealing pipe is H, wherein H=U/ rho * g, in the formula, U is pressure of crude benzene steam, rho is the density factor of the crude benzene steam, and g is acceleration of gravity. The upper end of the liquid sealing discharge pipe is connected with the lower end of the lower elbow pipe of the liquid sealing pipe, and the lower end of the liquid sealing discharge pipe is connected on a water discharge pipe at the bottom of a crude benzene separation groove. By means of the separation system for reducing the vapor-liquid entrainment of the vapor phase pipe of the debenzolization tower, vapor and liquid in the crude benzene steam escaping from the debenzolization tower can be effectively separated, liquid phase entrainment in a crude benzene vapor phase is greatly reduced after separation, and erosion corrosion of an inlet pipe of an oil-gas heat exchanger and erosion corrosion of a body of the oil-gas heat exchanger are lightened.