Multi-stage Bioreactor Process for Ethanol Production

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Solution Overview

Problem

Current microbial fermentation processes for producing ethanol from CO-containing substrates face challenges such as low productivity, high byproduct formation, and economic viability due to the production of metabolites like acetic acid, methane, and n-butanol, which reduces available carbon for ethanol production and increases operational costs through the need for complex membrane separation systems.

Innovation Solution

Implementing a multi-stage bioreactor process where a C1-containing substrate is fed in parallel to multiple bioreactors, and liquid products are fed in series, allowing for the avoidance of microorganism separation and recycle in most stages, thereby enhancing ethanol productivity and reducing byproduct formation.

Engineering Contradictions & Design Principles

VSEngineering Contradiction Analysis

1Productivity

If traditional single-stage fermentation processes are used to produce ethanol from CO-containing substrates, then the process is simple to operate, but ethanol productivity is low and byproduct formation is high

Engineering Contradiction:
Improveethanol productivityVSAvoidprocess complexity
Core Design Contradiction:
ProductivityVSDevice complexity

Solution Approach 1:

The fermentation process is divided into multiple sequential bioreactor stages, where each stage is optimized for specific metabolic outcomes. The first stage focuses on growth and initial ethanol production, while subsequent stages focus on ethanol recovery and minimal byproduct formation, thereby increasing overall productivity without requiring complex single-stage systems

Inventive Principle:
Principle #1Segmentation

Solution Approach 2:

The process transitions from a single-stage system to a multi-stage sequential system, adding the dimension of temporal and spatial progression. Liquid products flow sequentially through multiple bioreactors, allowing different operational conditions in each stage to optimize both productivity and selectivity

Inventive Principle:
Principle #17Another dimension (Dimensionality change)

2Reliability

If membrane separation systems are implemented to separate microorganisms for recycle, then microorganism retention is improved, but device complexity and operational costs increase

Engineering Contradiction:
Improvemicroorganism retentionVSAvoidseparation system complexity
Core Design Contradiction:
ReliabilityVSDevice complexity

Solution Approach 1:

The invention extracts and removes the complex membrane separation system entirely. Instead of retaining microorganisms through separation, the process allows microorganisms to naturally settle and be retained in the first bioreactor through gravity and flow dynamics, eliminating the need for expensive and complex membrane systems while maintaining reliable microorganism retention

Inventive Principle:
Principle #2Taking out (Extraction)

Solution Approach 2:

The system uses the natural settling and flow characteristics of the fermentation broth to achieve microorganism retention without external intervention. The liquid product flows sequentially through bioreactors, and microorganisms are retained in earlier stages through natural processes rather than mechanical separation

Inventive Principle:
Principle #25Self-service

3Quantity of substance

If CO-containing substrate is used as carbon source, then lower cost carbon resources are utilized, but byproduct formation (acetic acid, methane, n-butanol) increases reducing carbon efficiency

Engineering Contradiction:
Improvecarbon source utilizationVSAvoidbyproduct formation
Core Design Contradiction:
Quantity of substanceVSObject-generated harmful factors

Solution Approach 1:

The substrate conversion is segmented across multiple bioreactor stages, with the first stage handling growth and initial conversion, and subsequent stages optimized for ethanol production with minimal byproduct formation. This segmentation allows better control over metabolic pathways and reduces carbon loss to byproducts

Inventive Principle:
Principle #1Segmentation

Solution Approach 2:

Operational parameters such as substrate concentration, flow rate, and retention time are optimized in each bioreactor stage to favor ethanol production over byproduct formation. These parameter changes maximize carbon efficiency when using CO-containing substrates

Inventive Principle:
Principle #35Parameter changes

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 achieves high ethanol productivity with low byproduct formation, improved carbon source utilization, and increased process flexibility, reducing operational costs and complexity compared to traditional methods.

Implementation Method 1

the ability of micro-organism cultures to grow, with CO being the sole carbon source, was first discovered in 1903. This characteristic was later determined to reside in an organism's use of the acetyl coenzyme A (acetyl CoA) biochemical pathway of autotrophic growth (also known as the Woods-Ljungdahl pathway and the carbon monoxide dehydrogenase/acetyl CoA synthase (CODH/ACS) pathway)

Methodology Applied
Scientific EffectFermentation: Fermentation

Implementation Method 2

Anaerobic bacteria, such as those from the genus Clostridium, are known to produce ethanol from CO, CO2 and H2 via the acetyl CoA biochemical pathway

Methodology Applied
Scientific EffectAcetyl CoA pathway:

Data Source

PatentEP4198118A1Multi-stage bioreactor processes
Publication Date: 2023.06.21 LANZATECH NZ INC
  • EP4198118A1 patent drawingFigure 1
  • EP4198118A1 patent drawingFigure 2
  • EP4198118A1 patent drawingFigure 3

AI summary

Multi-stage, biological processes and systems for converting a C1 carbon source to desired end products are described. The processes comprise dividing a gaseous C1-containing substrate, in parallel, among multiple bioreactor stages. Liquid products are successively fed, in series, from a first bioreactor stage to downstream bioreactor stages. Operation can be simplified by avoiding the requirement for microorganism separation and recycle at each stage. In addition, overall vapor-liquid mass transfer for the combined stages is very favorable, leading to high end product productivity with comparably low byproduct metabolite productivity.