Microstructured Flow Channels for Polyether Alcohol Plug Flow

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Solution Overview

Problem

The preparation of polyether alcohols in microstructured reactors faces challenges with mass flow maldistribution due to increasing viscosity, requiring high pressures and complex reactor designs to maintain uniform product quality and yield.

Innovation Solution

A process utilizing microstructured flow channels with a characteristic dimension of 20 to 10,000 μm, acting as static mixers, to achieve ideal plug flow and improved distribution of the reaction mixture, reducing maldistribution and enabling higher yields and selectivities.

Engineering Contradictions & Design Principles

VSEngineering Contradiction Analysis

1Productivity

If microstructured reactors are used to prepare polyether alcohols, then reaction rates are greatly enhanced and product quality is improved, but mass flow maldistribution occurs due to increasing viscosity

Engineering Contradiction:
Improvereaction rateVSAvoidmass flow distribution
Core Design Contradiction:
ProductivityVSManufacturing precision

Solution Approach 1:

The reaction system is segmented into multiple parallel microchannels, each with characteristic dimensions of 10-1000 μm. This segmentation allows the reaction mixture to be distributed across numerous small channels, reducing the impact of viscosity increases on flow distribution while maintaining high reaction rates through the large surface-area-to-volume ratio of the microstructured architecture.

Inventive Principle:
Principle #1Segmentation

2Productivity

If high pressures are applied to achieve high reaction rates, then productivity is improved, but the reactor design becomes more complex and difficult to manufacture

Engineering Contradiction:
Improvereaction rateVSAvoidreactor design
Core Design Contradiction:
ProductivityVSDevice complexity

Solution Approach 1:

The reactor operates at elevated pressures (up to 800 bar) but uses simple, robust microstructured geometries with characteristic dimensions of 10-1000 μm that can be manufactured using standard techniques. The microstructured design allows high pressure operation without requiring complex pressure management systems, as the small channel dimensions naturally manage pressure distribution and flow characteristics.

Inventive Principle:
Principle #35Parameter changes

3Quantity of substance

If the reaction mixture viscosity increases during the reaction, then conversion progresses, but flow distribution among parallel channels deteriorates

Engineering Contradiction:
ImproveconversionVSAvoidflow distribution
Core Design Contradiction:
Quantity of substanceVSManufacturing precision

Solution Approach 1:

A distribution device is incorporated upstream of the microchannels to pre-distribute the reaction mixture uniformly across all channels before the viscosity increases significantly during the reaction. This preliminary distribution action ensures that even as the reaction progresses and viscosity rises, the flow remains well-distributed among the parallel microchannels, maintaining both conversion efficiency and flow uniformity.

Inventive Principle:
Principle #10Preliminary action

4Ease of manufacture

If traditional reactors are used, then manufacturing is simpler, but product quality and yield are lower due to maldistribution

Engineering Contradiction:
Improvereactor fabricationVSAvoidproduct quality
Core Design Contradiction:
Ease of manufactureVSManufacturing precision

Solution Approach 1:

The microstructured reactor uses repeating patterns of channels with characteristic dimensions of 10-1000 μm that can be manufactured by copying a single unit cell design multiple times. This copying approach allows complex microstructured geometries to be produced with high precision and uniformity using standard manufacturing techniques, achieving both ease of manufacture and high product quality through consistent flow distribution across all replicated channels.

Inventive Principle:
Principle #26Copying

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 approach enhances the uniformity of mass flow and product properties, achieving complete conversion and reducing high molecular weight by-products, while maintaining thermal homogeneity and reducing viscosity at the same molar mass compared to traditional methods.

Implementation Method 1

the flow profile of the liquid reaction mixture through the microstructured flow channels is approximate to an ideal plug flow

Methodology Applied
Scientific EffectPlug flow: Laminar Flow

Implementation Method 2

the reactor being operated at pressures of up to 800 bar and temperatures in the range from 30 to 400° C. In this way, the potential of very high reaction rates resulting from high alkylene oxide pressures can be optimally utilized

Methodology Applied
Scientific EffectPressure: Pressure Increase

Implementation Method 3

a heat exchange apparatus being provided

Methodology Applied
Scientific EffectHeat exchange: Heat Exchanger

Data Source

PatentUS9120731B2Process for preparing polyether alcohols
Publication Date: 2015.09.01 EHRFELD MIKROTECHNIK BTS GMBH
  • US9120731B2 patent drawing
  • US9120731B2 patent drawing
  • US9120731B2 patent drawing

AI summary

What is proposed is a process for preparing polyether alcohols by conversion of the following reactants: a) one or more alkylene oxides and optionally carbon dioxide and b) one or more H-functional starter substances, in the presence of a catalyst, to form a liquid reaction mixture, in a reaction unit (1), which is characterized in that the reaction unit (1) has internals (2) which form a multitude of microstructured flow channels which bring about multiple splitting of the liquid reaction mixture into component flow paths and recombination thereof in altered arrangement, the multiple splitting and recombination being repeated several times and the microstructured flow channels having a characteristic dimension which is defined as the greatest possible distance of any particle in the liquid reaction mixture from the wall of a flow channel closest to the particle, in the range from 20 to 10 000 μm, the result being that the flow profile of the liquid reaction mixture approximates to ideal plug flow as a result of the microstructured flow channels.