A method for reducing the inhibition effect of by-products in lignocellulose alkaline pretreatment liquid and preparation of cellulosic ethanol based on this method
A technology of lignocellulose and pretreatment liquid, applied in the direction of microorganism-based methods, biochemical equipment and methods, microorganisms, etc., can solve the problems of increasing process complexity, time-consuming, additional consumption of reagents and energy, and achieve the goal of promoting Industrial application, simple equipment requirements, and the effect of eliminating inhibition effects
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
Embodiment 1
[0033] GOD treatment of bagasse pretreated with 1% NaOH and fermentation to produce ethanol
[0034] S1: Accurately weigh 2.5 g of bagasse, add 1% NaOH solution at a liquid-solid ratio of 10:1 (substrate concentration 10% (w / v)), treat bagasse at 121°C for 1 hour, and cool at room temperature to obtain a pre- treatment fluid;
[0035] S2: Under sterile conditions, add commercially available concentrated phosphoric acid to the pretreatment solution, adjust the pH to about 5, then add 10U GOD, detoxify at 30°C, 200rpm for 24h;
[0036] S3: Under sterile conditions, add cellulase to the above pretreatment solution, and fix the ratio of enzyme addition to substrate at 6 mg enzyme / g substrate, then place it in a constant temperature shaker, hydrolyze at 45 °C, 160 rpm for 72 hours; During the hydrolysis process, samples were taken to measure the enzymatic hydrolysis of bagasse;
[0037] S4: Then add peptone to a final concentration of 20g / L, and insert the pre-activated Saccharom...
Embodiment 2
[0040] GOD treatment of 2% NaOH pretreated bagasse and fermentation to produce ethanol
[0041] S1: Accurately weigh 2.5 g of bagasse, add 2% NaOH solution at a liquid-solid ratio of 10:1 (substrate concentration 10% (w / v)), treat bagasse at 121°C for 1 hour, and cool at room temperature to obtain a pre- treatment fluid;
[0042] S2: Under sterile conditions, add commercially available concentrated phosphoric acid to the pretreatment solution, adjust the pH to about 5, then add 15U GOD, detoxify at 30°C, 200rpm for 24h;
[0043] S3: Under sterile conditions, add cellulase to the above pretreatment solution, and fix the ratio of enzyme addition to substrate at 6 mg enzyme / g substrate, then place it in a constant temperature shaker, hydrolyze at 45 °C, 160 rpm for 72 hours; During the hydrolysis process, samples were taken to measure the enzymatic hydrolysis of bagasse;
[0044] S4: Then add peptone to a final concentration of 20g / L, and insert the pre-activated Saccharomyces ...
Embodiment 3
[0047] GOD treatment of 3% NaOH pretreated bagasse and fermentation to produce ethanol
[0048] S1: Accurately weigh 2.5 g of bagasse, add 3% NaOH solution at a liquid-solid ratio of 10:1 (substrate concentration 10% (w / v)), treat bagasse at 121°C for 1 hour, and cool at room temperature to obtain a pre- treatment fluid;
[0049] S2: Under sterile conditions, add commercially available concentrated phosphoric acid to the pretreatment solution to adjust the pH to about 5, then add 25U GOD, detoxify at 30°C, 200rpm for 24h;
[0050] S3: Under sterile conditions, add cellulase to the above pretreatment solution, and fix the ratio of enzyme addition to substrate at 6 mg enzyme / g substrate, then place it in a constant temperature shaker, hydrolyze at 45 °C, 160 rpm for 72 hours; During the hydrolysis process, samples were taken to measure the enzymatic hydrolysis of bagasse;
[0051] S4: Then add peptone to a final concentration of 20g / L, and insert the pre-activated Saccharomyce...
PUM
Abstract
Description
Claims
Application Information
- R&D Engineer
- R&D Manager
- IP Professional
- Industry Leading Data Capabilities
- Powerful AI technology
- Patent DNA Extraction
Browse by: Latest US Patents, China's latest patents, Technical Efficacy Thesaurus, Application Domain, Technology Topic, Popular Technical Reports.
© 2024 PatSnap. All rights reserved.Legal|Privacy policy|Modern Slavery Act Transparency Statement|Sitemap|About US| Contact US: help@patsnap.com