Looking for breakthrough ideas for innovation challenges? Try Patsnap Eureka!

Preparation method of bisphenol F

A phenol and feed technology, applied in the field of bisphenol F preparation, can solve the problems of short catalyst life, many side reactions, low product yield, etc., to increase the probability of contact and mass transfer efficiency, improve reaction efficiency and conversion rate , Improve the effect of condensation reaction conversion rate

Active Publication Date: 2019-04-26
CHINA PETROLEUM & CHEM CORP +1
View PDF12 Cites 0 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0005] CN104326878A discloses a method for catalytically synthesizing bisphenol F with nitric acid and phosphoric acid. This method uses nitric acid and phosphoric acid as catalysts, and uses an organic solvent to participate in the synthesis reaction. There are problems of corrosion, pollution and difficult separation
CN102584541A discloses a method for preparing bisphenol F with 1-alkyl-3-methylimidazole acidic ionic liquid. The method uses an ionic liquid catalyst. Although there are no problems such as corrosion and pollution, the catalyst needs to be recycled and energy consumption is high. Higher, and the catalyst life is short, and the product yield in the later stage of use is low
JP11269113 discloses a method for synthesizing bisphenol F using zeolite molecular sieves as a catalyst; CN 101987812A discloses a method for synthesizing bisphenol F using mesoporous molecular sieves as a catalyst. This type of method product separation and catalyst recovery are relatively easy, but the phenol-formaldehyde ratio and The reaction temperature is high, the reaction is difficult to control, and there are many side reactions

Method used

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
View more

Image

Smart Image Click on the blue labels to locate them in the text.
Viewing Examples
Smart Image
  • Preparation method of bisphenol F
  • Preparation method of bisphenol F

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0032] 1. Preparation of modified ion exchange resin catalyst: a: Wash 150 grams of styrene-based strongly acidic cation exchange resin with deionized water for 5 times, each time for 10 minutes, and dry it in a vacuum oven at 90°C for 4 hours; b: Put the dried strongly acidic cation exchange resin into a 2mm thick steel mesh bag, lay it flat on an ultrasonic vibrator with a vibration frequency of 59kHz, spray phosphotungstic acid aqueous solution with a mass percentage of 40% and nitrogen with an atomizing nozzle Immerse for 2 hours, the spray distance is 1cm, and the spray pressure is 0.05MPa; c: After washing, put it in a vacuum oven for 6 hours at 90°C, and bake the dried ion exchange resin at 210°C for 8 hours; d: Then put The resin is treated with 20% phosphotungstic acid aqueous solution according to the method of b, after washing, it is dried in a vacuum oven at 80°C for 6 hours, and the dried ion exchange resin is calcined at 200°C for 8 hours to obtain the supported ...

Embodiment 2

[0035] 1. Preparation of modified ion exchange resin catalyst: a: Wash 150 grams of styrene-based strongly acidic cation exchange resin with deionized water for 5 times, each time for 10 minutes, and dry it in a vacuum oven at 90°C for 6 hours; b: Put the dried strongly acidic cation exchange resin into a steel mesh bag with a thickness of 3mm, lay it flat in an ultrasonic vibrator with a vibration frequency of 58kHz, spray phosphotungstic acid aqueous solution with a mass percentage of 35% and nitrogen with an atomizing nozzle Immerse for 2 hours, the spray distance is 2cm, and the spray pressure is 0.07MPa; c: After washing, put it in a vacuum oven for 6 hours at 90°C, and bake the dried ion exchange resin at 210°C for 8 hours; d: Then put The resin is treated with 20% phosphotungstic acid aqueous solution according to the method of b, after washing, it is dried in a vacuum oven at 80°C for 6 hours, and the dried ion exchange resin is calcined at 200°C for 8 hours to obtain t...

Embodiment 3

[0038] 1. Preparation of modified ion exchange resin catalyst: a: Wash 150 grams of styrene-based strongly acidic cation exchange resin with deionized water for 5 times, each time for 10 minutes, and dry it in a vacuum oven at 90°C for 6 hours; b: Put the dried strongly acidic cation exchange resin into a steel mesh bag with a thickness of 3 mm, lay it flat on an ultrasonic vibrator with a vibration frequency of 57 kHz, spray phosphotungstic acid aqueous solution with a mass percentage of 45% and nitrogen with an atomizing nozzle Immerse for 2 hours, spray distance 2cm, spray pressure 0.06MPa; c: After washing, dry in a vacuum oven at 90°C for 6 hours, and bake the dried ion exchange resin at 210°C for 8 hours; d: Then put The resin is then treated with 15% phosphotungstic acid aqueous solution according to the method b, after washing, it is dried in a vacuum oven at 80°C for 6 hours, and the dried ion exchange resin is calcined at 200°C for 8 hours to obtain the supported het...

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to View More

PUM

No PUM Login to View More

Abstract

The invention discloses a preparation method of bisphenol F. The preparation method comprises the following steps that a fixed-bed tubular reactor is provide with a separation plate in the axial direction to divide the reactor into three parts, two sides of the separation plate are an upper feeding section and a discharging section, and the lower part of the separation plate is a lower feeding section; an aqueous solution of phenol and an aqueous solution of formaldehyde are fed as feed I from a raw material inlet of the upper feeding section into the reactor, and the aqueous solution of phenol and nitrogen are fed into the reactor as feed II from a raw material inlet of the lower feeding section; the feed I is subjected to a condensation reaction in a catalyst bed in the middle part of the reactor, the reacted materials are mixed with the bottom-up feed II for further reaction, and a reaction product is discharged from a discharging port of the discharging section, then separated andpurified to obtain the bisphenol F. The preparation method uses phenol and formaldehyde as raw materials, the reactor adopts the fixed-bed tubular reactor with the separation plate in the middle, andthe feeding mode adopts a method of upper and lower feeding simultaneously. The preparation method of the bisphenol F is simple in process, high in efficiency and mild in conditions, catalyst activityis stable and long-term operation can be achieved.

Description

technical field [0001] The invention relates to a method for preparing bisphenol F, in particular to a method for preparing bisphenol F by using phenol and formaldehyde as raw materials. Background technique [0002] Bisphenol F, also known as bis-(hydroxyphenyl)methane, molecular formula C13H12O2, melting point 160 ° C, ultraviolet light can cause discoloration, it is a white leaf-shaped crystal. It is a monomer for synthetic materials, mainly used in the synthesis of epoxy resins, and can also be used in the synthesis of polycarbonate resins, polyester resins and phenolic resins, flame retardants, antioxidants and surfactants. Epoxy resin is the matrix material of high-performance composite materials. It has various types and excellent performance. It has good adhesion, insulation, chemical stability and thermal stability. It is easy to cure and has a wide range of uses. At present, common epoxy resins mainly include glycidyl ether resins—bisphenol A epoxy resins. As a m...

Claims

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to View More

Application Information

Patent Timeline
no application Login to View More
IPC IPC(8): C07C37/20C07C39/16B01J31/34B01J31/18B01J37/02B01J37/34
CPCC07C37/20B01J31/34B01J37/0201B01J37/343C07C39/16Y02P20/52
Inventor 刘野霍稳周吕清林李花伊
Owner CHINA PETROLEUM & CHEM CORP
Who we serve
  • R&D Engineer
  • R&D Manager
  • IP Professional
Why Patsnap Eureka
  • Industry Leading Data Capabilities
  • Powerful AI technology
  • Patent DNA Extraction
Social media
Patsnap Eureka Blog
Learn More
PatSnap group products