31 results about "Olefiant gas" patented technology

The invention discloses a technology for separating low carbon olefin gases, for solving the problems that hydrogen, methane, ethane and propane and other products with high purity can not be acquired and dimethyl ether and oxygen and carbon monoxide in impurities are not removed efficiently, etc. in the prior art. The technology is characterized in that a step of removing carbon monoxide and oxygen is added, methanol-to-olefin gas streams processed by removing carbon monoxide and oxygen enter into a deethanizing column, deethanizing column overhead streams successively pass through an ethene hydrogenation reactor, six separation pots, a low pressure demethanizing column and an ethene rectification column, etc. to separate to obtain ethene and ethane products, and deethanizing column bottom streams successively pass through a propyne hydrogenation reactor, a methane stripper and a propylene rectification column, etc. to separate to obtain propylene and propane products. According to the invention, polymer grade ethene and propylene products can be obtained, and hydrogen, methane, ethane and propane products, etc. with high purity can be obtained.

The invention relates to a preparation method of high-isotacticity polybutene-1 powder. The method comprises the following steps: sequentially adding a cocatalyst solution, an outer electron donor, a main catalyst, an assistant compound and a liquid-phase alpha-olefin into a tank reactor, prepolymerizing at 10-90 DEG C for 10-120 minutes, evacuating olefin gas, charging butylene-1 monomer and molecular weight regulator hydrogen gas, polymerizing at -10-90 DEG C for 1-20 hours, and carrying out flash evaporation on the unreacted monomer to obtain the high-isotacticity polybutene-1 powder. The polymerization method for synthesizing high-isotacticity polybutene-1 and powder thereof is simple in technique and easy to operate. The prepolymerization method solves the problem of difficulty in controlling the form of the polybutene-1 in the common catalytic polymerization method, and improves the problem of long crystal form transition period of the polybutene-1.

The invention discloses a separation process for preparing low-carbon olefin gas through methanol conversion, aiming at overcoming the defects that products such as high-purity hydrogen, methane, ethane and propane cannot be obtained, dimethyl ether and oxygen and carbon monoxide in flue gas impurities are not effectively removed and the like in the prior art. A carbon monoxide and oxygen removal step is added in the process. Methanol-to-olefin gas with the carbon monoxide and the oxygen being removed passes through six separation tanks and then enters a high-pressure demethanation tower, a deethanization tower, an acetylene hydrogenation reactor, an ethylene rectifying tower, an allylene hydrogenation reactor, a propylene rectifying tower and the like for separation, wherein liquid which comes out from the bottoms of the first five separation tanks sequentially enters the middle-to-upper part of the demethanation tower. By adopting the separation process, polymer-grade ethylene and propylene products can be obtained and products such as high-purity hydrogen, methane, ethane and propane can also be obtained.

The invention discloses a separation method for preparing low-carbon olefin gas through methanol conversion, and aims to solve the problems that products with high purity such as hydrogen, methane, ethane and propane which cannot be obtained in the prior art and oxygen, carbon oxide and the like in dimethyl enther and gas impurities cannot be effectively removed. According to the method, a step of removing the carbon oxide and the oxygen is increased, a methanol prepared olefin gas material flow from which the carbon oxide and the oxygen are removed enters a deethanizing column; the material flow on the top of the deethanizing column flows through an acetylene hydrogenation reactor, six separation tanks, a demethanizing column, an ethylene rectifying column and the like in sequence to separate to obtain ethylene and ethane products; and the material flow at the bottom of the deethanizing column flows through a propyne hydrogenation reactor, a methane stripping column, a propylene rectifying column and the like in sequence to separate to obtain propene and propane products. By using the separation method, polymer grade ethylene and propene products can be obtained, and products with high purity such as hydrogen, methane, ethane and propane can also be obtained.

An olefin gas leakage monitoring system and a method thereof. The monitoring system contains a detection unit for detecting and imaging an area to be detected, an analytical unit, a control and drive unit and an alarm unit. The detection unit contains an infrared thermal imager which contains an olefin gas recognizer. The analytical unit contains an image preanalysis module and an image qualitative analysis module, wherein the image preanalysis module is used for analyzing an image detected by the detection unit before the olefin gas recognizer is started and judging whether it is a gas; and the image qualitative analysis module is used for recognizing and analyzing the image detected by the detection unit after the olefin gas recognizer is started and judging whether it is an olefin gas. The control and drive unit is connected with the detection unit and the analytical unit and is used for controlling and driving the olefin gas recognizer according to an analysis result of the analytical unit. The monitoring system and the method disclosed in the invention are used for online monitoring of olefin gas leakage. By the system and the method, olefin gas leakage can be detected timely and accurately, and safety and continuity of the production can be guaranteed.

A liquefied petroleum gas containing propane or butane as a main component is produced by passing a raw material gas comprising hydrogen and at least one selected from the group consisting of methanol and dimethyl ether through a catalyst layer comprising, in the direction of flowing of the raw material gas, a former catalyst layer comprising a catalyst for synthesizing an olefin-containing gas which is used when producing an olefin-containing gas from at least one selected from the group consisting of methanol and dimethyl ether, and a latter catalyst layer comprising a catalyst for hydrogenating an olefin-containing gas which is used when an olefin is hydrogenated to produce a paraffin.

The invention provides an equipment for producing carbon nanotubes with a fluidized bed and a preparation method thereof. The equipment includes a main reaction furnace, a gas distributor, a fluidized bed and a gas-solid separator. The bottom of the main reaction furnace is provided with a carbon source gas inlet , the gas distributor is set on the upper side of the carbon source gas inlet and installed at the bottom of the fluidized bed; the outer wall of the main reaction furnace at the top of the fluidized bed is obliquely provided with a catalyst inlet, and the outer wall of the main reaction furnace at the middle and lower part of the fluidized bed is inclined A carbon nanotube outlet is arranged downward; the preparation method includes the following steps: directly sending the prepared mixed metal oxide catalyst into the fluidized bed in the main reaction furnace; Inside, olefin gas with less than 4 carbons is introduced to obtain carbon nanotubes with a diameter of 4-80 nanometers and a length of 0.5-200 microns, which are discharged from the outlet; the equipment is simple in structure, easy to operate, and low in energy consumption, and is suitable for continuous Chemical production of carbon nanotubes with an annual output of 1,000 tons.

The invention provides a detection device and method for an olefin gas. The detection device includes: an infrared optical lens, which is used for focusing infrared radiation signals; an olefin gas recognizer, which includes a turntable and at least one olefin band pass filter plate disposed on the turntable; an infrared detector, which is used for converting infrared radiation signals passing through the olefin band pass filter plate into voltage signals so as to form an infrared image; a monitoring and analysis unit, which is used for acquiring and analyzing the infrared image, outputting the analysis result, and controlling the turntable of the olefin gas recognizer according to the analysis result; and a display, which is connected to the output end of the monitoring and analysis unit and is used for displaying the output result. Compared with the prior art, the olefin gas detection device and method provided by the invention are based on an infrared imaging technology, and can visually judge whether a to-be-detected target is an olefin gas accurately and quickly.

A liquefied petroleum gas containing propane or butane as a main component is produced by passing a raw material gas comprising hydrogen and at least one selected from the group consisting of methanol and dimethyl ether through a catalyst layer comprising, in the direction of flowing of the raw material gas, a former catalyst layer comprising a catalyst for synthesizing an olefin-containing gas which is used when producing an olefin-containing gas from at least one selected from the group consisting of methanol and dimethyl ether, and a latter catalyst layer comprising a catalyst for hydrogenating an olefin-containing gas which is used when an olefin is hydrogenated to produce a paraffin.

The invention belongs to the field of organic chemical industry, and provides a green synthesis method for preparing alcohol ether by using olefin in one step. The green synthesis method is characterized in that a jet type reactor is used for continuously jetting alcohol, hydrogen peroxide and a cyclization-alcoholysis catalyst into a pressured reaction kettle filled with olefin gas, so that continuous epoxidation and alcoholysis reaction is carried out; after being separated by a ceramic membrane, reaction liquid enters to an olefin and alcohol removal tower; after olefin and alcohol are removed, the reaction liquid directly and continuously enters to a rectifying tower, and the alcohol ether product is obtained by rectifying; the effective utilization rate of the hydrogen peroxide is more than or equal to 98%, the alcohol ether selectively is greater than or equal to 99%, and the product purity is higher than or equal to 99.5%. The green synthesis method can be used for preparing the alcohol ether in one step and is suitable for industrial large-scale production.

The invention belongs to the technical field of communication and relates to a mobile phone device capable of measuring the concentration of inflammable gases. The mobile phone device comprises a mobile phone body, a battery, a user identity recognition card, a data processing system, a wireless signal receiving and transmitting system, an alkane gas concentration measuring device, an olefin gas concentration measuring device, an alkyne gas concentration measuring device, a hydrogen sulfide gas concentration measuring device and a hydrogen concentration measuring device, wherein the battery, the user identity recognition card, the data processing system, the wireless signal receiving and transmitting system and the inflammable gas concentration measuring devices are arranged on the mobile phone body. The mobile phone device achieves the basic functions of calling and short messages, and meanwhile the concentration of the inflammable gases in the environment where a user is located can be synchronously measured. The mobile phone device is reasonable in design, simple in structure and capable of achieving multiple measuring functions.

The invention discloses a hydrothermal lithium iron phosphate carbon coating method which includes the steps: first, placing lithium iron phosphate prepared by a hydrothermal method in air atmosphere and heating and drying the lithium iron phosphate for 1-3 hours; second, placing the dried lithium iron phosphate in a high-temperature furnace, keeping the temperature of 570-600 DEG C for 1-2 hours in protective gas atmosphere, leading reaction gas at the temperature of 600-650 DEG C, performing reaction for 4-6 hours, switching the reaction gas into protective gas and cooling the lithium iron phosphate to below 100 DEG C to obtain a LiFePO4/C composite material. The reaction gas is prepared by mixing olefin gas with the protective gas. A carbon coating layer with uniform components, controllable thickness and good conductivity can be obtained under the catalytic action of Fe3+ on the surface of LiFePO4 for olefin carbonization. The material has excellent electrochemical performance, and tap density can be improved.

The invention discloses a separation device and a separation method for methanol-to-olefin gas. According to the method, methanol-to-olefin gas is pretreated through a pretreatment assembly (1); phaseseparation is carried out in a separator (2); the condensate is conveyed to a condensate dryer (3); the gas phase is conveyed to a first gas phase dryer (4), and is dried, and the dried material is conveyed to an ethane removal tower (5); the tower top gas phase of the ethane removal tower (5) passes through a methanol removal tower (6), a solvent recovery tower (7), an acetylene converter (8) and an ethylene rectifying tower (9) to separate ethylene; and the tower bottom of the ethane removal tower (5) passes through a propane removal tower (10) and a propylene rectifying tower (11) to separate propylene. According to the method, the circulation loop of the absorbent comprises a methanol removal tower (6), a solvent recovery tower (7) and a methanol removal tower (6), so that the circulation loop is short, does not uses an ethane removal tower (5) and a propylene rectifying tower (11), and effectively reduces the load, the energy consumption and the equipment investment of the ethaneremoval tower (5) and the propylene rectifying tower (11).

The invention discloses a methanol-to-olefin preparation gas separation process. According to the invention, a pre-C3-removing process is adopted, and an absorbent separation tower is arranged before a methane-removing tower, such that a material is preliminarily separated. Two streams of different absorbents are adopted in the methane-removing tower, and enter the tower from different positions on the upper part. A main absorbent is a tower kettle material from the absorbent separation tower, and the other stream of absorbent is C2, C3 or a mixture of hydrocarbons thereof from subsequent systems. Compared to prior arts, the process has the advantages of low investment, low energy consumption, high material recovery rate, simple operation, and the like.

The invention belongs to the field of catalysts, and especially relates to an ex-situ presulfuration method for a hydrogenation catalyst. The method concretely comprises the following steps: immersingthe hydrogenation catalyst in an organic solvent containing industrial vitamin C, and carrying out reduction pretreatment at 80-100 DEG C for 5-10 h; adding sulfur and ammonia water having a concentration of 23-25% into a reactor, heating the added substances to 120-140 DEG C, and carrying out a reaction for 3-4 h to generate ammonium polysulfide; introducing an olefin gas into the reactor, carrying out heat insulation treatment under a pressure of 5-10 MPa for 24-36 h; cooling the reactor to room temperature after the reaction is finished in order to obtain a sulfuration agent; and adding the pretreated catalyst to the sulfuration agent, adding the olefin gas, carrying out heat treatment to sufficiently sulfurate the catalyst, passivating the sulfurated catalyst in a container filled aninert gas, and carrying out constant temperature treatment for 10-12 h. The method has the advantages of simplicity in process operation, low cost and small in environmental pollution, and is suitablefor industrial production.

The invention relates to an alkylation method, which comprises the following steps: mixing isobutane and C3-C5 olefin gas to form mixed raw material gas, dispersing concentrated sulfuric acid into liquid drops with the size of 0.001-500 [mu]m, mixing the mixed raw material gas with the concentrated sulfuric acid liquid drops, and then carrying out quenching treatment under the conditions that the temperature is -20 to 20 DEG C and the pressure is 0.1-1 MPa, so that the mixed raw material gas is subjected to phase change condensation and is kept for 0.1-10 seconds; and the reaction temperature is adjusted to -20 DEG C to 10 DEG C, the reaction pressure is kept to be 0.1-1 MPa, and the materials are subjected to an alkylation reaction. The method comprises the following steps: mixing a mixed raw material gas with finely dispersed sulfuric acid liquid drops, condensing the raw material gas on the surface of the sulfuric acid liquid drops under a quenching condition to form reaction liquid drops, further controlling the reaction conditions, taking sulfuric acid as a catalyst, enabling the condensed raw material gas to quickly generate alkylation reaction, and enabling olefin and alkane to react according to a molecular ratio close to 1:1, so that side reactions are reduced, and the alkylation reaction efficiency is improved.