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Technology of preparing hydrocarbons produce from methanol by one-step method

A technology for hydrocarbon products and methanol, which is applied in the field of one-step conversion of methanol to produce hydrocarbon products, can solve the problems of large investment, large number of reactors, long process flow, etc., and achieves low investment, short process flow and simple operation. Effect

Active Publication Date: 2007-03-07
SHANXI INST OF COAL CHEM CHINESE ACAD OF SCI +2
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0008] Regardless of the use of fixed bed or fluidized bed reactors, the two-stage methanol conversion technology to produce hydrocarbon products has the disadvantages of long process flow, large number of reactors, and large investment.

Method used

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  • Technology of preparing hydrocarbons produce from methanol by one-step method

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0041] A. Synthesis of Directing Agents

[0042] The molar ratio composition of the directing agent is SiO 2 : Al 2 o 3 :Na 2 O: n-Butylamine: H 2 SO 4 :H 2 O=40:1:10:28:7.2:2800. The composition of the silicon source is: SiO 2 = 25.13%; Na 2 O = 8.12%; H 2 O=66.75% water glass, first take by weighing 600 grams of water glass, add 126.5 grams of n-butylamine and 1181.3 grams of deionized water to make A solution, put it into the synthesis kettle, under stirring at 300 rpm Stir evenly, then weigh 41.82 grams of aluminum sulfate, put it into a beaker containing 1561.4 grams of water, then add 15.8 grams of sulfuric acid, stir evenly with a glass rod, make B solution, and add it dropwise to the solution in the kettle , Then the still is sealed, continue to stir and start to heat up after 10-20 minutes. In the first step, the temperature is raised from room temperature to 120°C at a rate of 2°C / min for 20 hours, and in the second step, the temperature is raised to 165°C a...

Embodiment 2

[0052] A. Synthesis of Directing Agents

[0053] The raw material composition of the directing agent is SiO 2 : Al 2 o 3 :Na 2 O: 1.6-hexanediamine: H 2 SO 4 :H 2 O=60:1:13:32:3.3:3000. The composition of the silicon source is: SiO 2 = 25.13%; Na 2 O = 8.12%; H 2 O=66.75% water glass, at first take by weighing 600 grams of water glass, add 728.9 grams of deionized water and 149.9 grams of 1,6-hexamethylenediamine to make A solution into the synthesis kettle, at 300 rpm Stir evenly under stirring, then weigh 17.93 grams of aluminum nitrate, put it into a beaker with 1561.4 grams of water, then add 15.6 grams of sulfuric acid, stir it with a glass rod to make B solution, add it dropwise to the solution, then the kettle was sealed, and the temperature began to rise after continuing to stir for 10-20 minutes. In the first step, the temperature is raised from room temperature to 120°C at a rate of 2°C / min for 20 hours, and in the second step, the temperature is raised to...

Embodiment 3

[0061] A. Synthesis of Directing Agents

[0062] The raw material composition of the directing agent is SiO 2 : Al 2 o 3 :Na 2 O: Ethylamine: H 2 SO 4 :H 2 O=80:1:15:38:5.2:3800

[0063] The composition of the silicon source is: SiO 2 = 25.13%; Na 2 O = 8.12%; H 2 O=66.75% water glass, first take by weighing 600 grams of water glass, add 84.33 grams of ethylamine and 1181.3 grams of deionized water to make A solution, put it into a synthesis kettle, and stir evenly under stirring at 300 rpm , then weigh 41.82 grams of aluminum sulfate, put it into a beaker with 1561.4 grams of water, then add 15.8 grams of sulfuric acid, stir it with a glass rod to make B solution, add it dropwise to the solution in the kettle, and then The kettle was sealed, and the stirring was continued for 10-20 minutes, and then the temperature began to rise. In the first step, the temperature is raised from room temperature to 120°C at a rate of 2°C / min for 20 hours, and in the second step, th...

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Abstract

The invention discloses a preparing method of hydrocarbon based on once carbinol, which comprises the following steps: heating carbinol to reacting temperature; entering into the reactor with acid siallite zeolite molecular sieve catalyst; transmitting into hydrocarbon compound at 300-500 deg.c under 0.1-5.0 Mpa with the speed at 0.1-10.0h-1; cooling; separating the C5+ hydrocarbon product and gas phase part; entering gas phase in the compressor; making partial liquid leave system; adopting others as circulating material to blend with raw carbinol; returning to reactor to proceed next reaction.

Description

technical field [0001] The invention relates to a method for producing hydrocarbon products by one-step conversion of methanol, technical background [0002] At present, the international crude oil price continues to rise, and one of the important factors is the arrival of the foreseeable peak of oil production, which triggers an international upsurge of research on alternative energy technologies. my country's energy structure is characterized by rich coal, little gas, and oil shortage. Therefore, for our country, from the perspective of energy security strategy, the demand for developing alternative energy is more urgent. [0003] Methanol is the cornerstone of petrochemical industry. Through proper catalytic process, methanol can be converted into various products of petrochemical industry, such as ethylene, propylene, aromatic hydrocarbons, alkanes and mixtures of the above products. [0004] Methanol conversion to gasoline (MTG) technology is a methanol conversion tech...

Claims

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Application Information

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Patent Type & Authority Applications(China)
IPC IPC(8): C07C1/20
Inventor 李文怀张庆庚胡津仙潘国平程建斌袁斌杨挺张侃张建得方勇
Owner SHANXI INST OF COAL CHEM CHINESE ACAD OF SCI
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