Thermal Decomposition Reactor for HFO-1234yf Production

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Solution Overview

Problem

Current methods for producing 2,3,3-tetrafluoropropene (HFO-1234yf) face challenges such as high installation costs, difficult distillation and purification of intermediate and final products, low yield of highly pure HFO-1234yf due to byproduct formation, and reactor corrosion issues.

Innovation Solution

A process involving the thermal decomposition of chlorodifluoromethane, chloromethane, and tetrafluoroethylene in a reactor with a heat medium at 400 to 1200°C, using steam, nitrogen, or carbon dioxide, to produce HFO-1234yf and 1,1-difluoroethylene directly, reducing byproduct formation and enabling high yield and purity.

Engineering Contradictions & Design Principles

VSEngineering Contradiction Analysis

1Ease of manufacture

If multistage reactions are used to produce HFO-1234yf, then the production process can achieve the target product, but the installation costs increase and distillation/purification becomes difficult

Engineering Contradiction:
Improveproduction process simplicityVSAvoidinstallation costs
Core Design Contradiction:
Ease of manufactureVSDevice complexity

Solution Approach 1:

The patent combines multiple reaction steps into a single reactor system where chlorodifluoromethane, chloromethane, and tetrafluoroethylene undergo thermal decomposition and condensation reactions simultaneously at 845±5°C to directly produce HFO-1234yf, eliminating the need for separate reaction stages and intermediate product handling

Inventive Principle:
Principle #5Merging (Combining)

Solution Approach 2:

The patent segments the reaction process by using a phase-transfer catalyst that operates in a specific temperature range (845±5°C) to facilitate the condensation reaction between gaseous intermediates, allowing the complex multistage process to be conducted in one reactor with controlled conditions

Inventive Principle:
Principle #1Segmentation

2Productivity

If thermal decomposition is conducted at high temperature to form HFO-1234yf, then the reaction proceeds efficiently, but byproducts such as CTFE are formed which are difficult to separate by distillation

Engineering Contradiction:
Improvereaction efficiencyVSAvoidproduct purity
Core Design Contradiction:
ProductivityVSManufacturing precision

Solution Approach 1:

The patent precisely controls the reaction temperature at 845±5°C and adjusts the molar ratio of raw materials (chlorodifluoromethane:chloromethane:tetrafluoroethylene) to optimize the formation of HFO-1234yf while minimizing byproduct CTFE generation, enabling effective separation by distillation

Inventive Principle:
Principle #35Parameter changes

Solution Approach 2:

The patent introduces a phase-transfer catalyst as an intermediary substance that facilitates the condensation reaction between gaseous intermediates at the specified temperature, promoting selective formation of HFO-1234yf and reducing unwanted byproducts

Inventive Principle:
Principle #24Intermediary (Mediator)

3Productivity

If retention time is increased to improve reaction completeness, then more HFO-1234yf is formed, but high boiling products and carbonization occur blocking the reactor

Engineering Contradiction:
Improvereaction completenessVSAvoidreactor blockage
Core Design Contradiction:
ProductivityVSObject-generated harmful factors

Solution Approach 1:

The patent maintains the reaction at a specific temperature (845±5°C) with controlled retention time to achieve complete reaction without excessive heating that would cause carbonization, using periodic monitoring and adjustment to prevent reactor blockage

Inventive Principle:
Principle #19Periodic action

4Ease of manufacture

If common heating means such as electric heater is used, then the reaction can be conducted, but acid component byproducts cause corrosion requiring special corrosion resistant apparatus

Engineering Contradiction:
Improveprocess feasibilityVSAvoidreactor corrosion
Core Design Contradiction:
Ease of manufactureVSObject-affected harmful factors

Solution Approach 1:

The patent uses a phase-transfer catalyst that can be easily replaced or regenerated, and the reaction conditions are optimized to minimize acid byproduct formation, reducing the need for expensive corrosion-resistant materials like platinum-lined reactors

Inventive Principle:
Principle #27Cheap short-living objects (Disposable)

Applied Scientific Principles

This section explains which scientific principles are used to turn an abstract innovation direction into a practical engineering solution.

Function Achieved in This Case

This process significantly reduces production costs and facility requirements, achieves high yield and purity of HFO-1234yf, and produces 1,1-difluoroethylene, while minimizing byproduct formation and reactor issues, making it economically viable and industrially practical.

Implementation Method 1

a process for producing 2,3,3,3-tetrafluoropropene (HFO-1234yf) and 1,1-difluoroethylene (VdF) by one reaction from raw material comprising chlorodifluoromethane, chloromethane and tetrafluoroethylene

Methodology Applied
Scientific EffectThermal decomposition: Pyrolysis

Data Source

PatentEP2826765B1Production method for 2,3,3,3-tetra-fluoropropene and 1,1-difluoroethylene
Publication Date: 2020.01.22 AGC INC
  • EP2826765B1 patent drawingFigure 1
  • EP2826765B1 patent drawingFigure 2
  • EP2826765B1 patent drawing

AI summary

To provide an economically advantageous process for producing HFO-1234yf useful as a new refrigerant in sufficiently high yield by one reaction involving thermal decomposition. A process for producing HFO-1234yf and VdF from raw material containing R22, R40 and TFE, by a synthetic reaction involving thermal decomposition, which comprises (a) a step of supplying the R22, the R40 and the TFE to a reactor, as preliminarily mixed or separately, (b) a step of supplying a heat medium to the reactor, and (c) a step of bringing the heat medium in contact with the R22, the R40 and the TFE in the reactor to form the HFO-1234yf and the VdF.