CN112553269A - Pretreatment and enzymolysis method of corn straw - Google Patents

Pretreatment and enzymolysis method of corn straw Download PDF

Info

Publication number
CN112553269A
CN112553269A CN202011550711.8A CN202011550711A CN112553269A CN 112553269 A CN112553269 A CN 112553269A CN 202011550711 A CN202011550711 A CN 202011550711A CN 112553269 A CN112553269 A CN 112553269A
Authority
CN
China
Prior art keywords
pretreating
steps
following
solid
pretreatment
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Pending
Application number
CN202011550711.8A
Other languages
Chinese (zh)
Inventor
徐建
顾帅令
吴海军
左宗涛
魏无忌
胡世杰
张楷
徐霞
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Anhui University of Technology AHUT
Original Assignee
Anhui University of Technology AHUT
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Anhui University of Technology AHUT filed Critical Anhui University of Technology AHUT
Priority to CN202011550711.8A priority Critical patent/CN112553269A/en
Publication of CN112553269A publication Critical patent/CN112553269A/en
Pending legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C12BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12PFERMENTATION OR ENZYME-USING PROCESSES TO SYNTHESISE A DESIRED CHEMICAL COMPOUND OR COMPOSITION OR TO SEPARATE OPTICAL ISOMERS FROM A RACEMIC MIXTURE
    • C12P19/00Preparation of compounds containing saccharide radicals
    • C12P19/14Preparation of compounds containing saccharide radicals produced by the action of a carbohydrase (EC 3.2.x), e.g. by alpha-amylase, e.g. by cellulase, hemicellulase
    • CCHEMISTRY; METALLURGY
    • C12BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12PFERMENTATION OR ENZYME-USING PROCESSES TO SYNTHESISE A DESIRED CHEMICAL COMPOUND OR COMPOSITION OR TO SEPARATE OPTICAL ISOMERS FROM A RACEMIC MIXTURE
    • C12P19/00Preparation of compounds containing saccharide radicals
    • C12P19/02Monosaccharides
    • CCHEMISTRY; METALLURGY
    • C12BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12PFERMENTATION OR ENZYME-USING PROCESSES TO SYNTHESISE A DESIRED CHEMICAL COMPOUND OR COMPOSITION OR TO SEPARATE OPTICAL ISOMERS FROM A RACEMIC MIXTURE
    • C12P2201/00Pretreatment of cellulosic or lignocellulosic material for subsequent enzymatic treatment or hydrolysis
    • CCHEMISTRY; METALLURGY
    • C12BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12PFERMENTATION OR ENZYME-USING PROCESSES TO SYNTHESISE A DESIRED CHEMICAL COMPOUND OR COMPOSITION OR TO SEPARATE OPTICAL ISOMERS FROM A RACEMIC MIXTURE
    • C12P2203/00Fermentation products obtained from optionally pretreated or hydrolyzed cellulosic or lignocellulosic material as the carbon source
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02PCLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
    • Y02P20/00Technologies relating to chemical industry
    • Y02P20/50Improvements relating to the production of bulk chemicals
    • Y02P20/54Improvements relating to the production of bulk chemicals using solvents, e.g. supercritical solvents or ionic liquids

Abstract

The invention discloses a method for pretreatment and enzymolysis of corn straws, which comprises the following steps: the method comprises the following steps: cutting corn stalks, and sequentially crushing, washing and drying to obtain particles; adding the particles into a dilute sulfuric acid solution, pretreating for a period of time under the condition of supercritical carbon dioxide, filtering, collecting filtrate and filter residues, and drying the filter residues in an oven for a period of time to remove moisture to obtain a solid matter; and (3) taking the solid as an enzyme hydrolysis substrate, adding xylanase and trisodium citrate buffer solution according to a certain solid-to-liquid ratio, and performing enzyme hydrolysis for a period of time to obtain xylose. The method disclosed by the invention is scientific and reasonable in design, and the effect of the supercritical carbon dioxide pretreatment is enhanced by using the dilute acid at a low temperature, so that the complex cross-linked structure of the lignocellulose is broken better, the chemical bond between the lignin and the hemicellulose is broken, the lignin is removed, more hemicellulose is exposed, and the enzymatic hydrolysis efficiency is improved.

Description

Pretreatment and enzymolysis method of corn straw
Technical Field
The invention relates to the technical field of agricultural waste conversion and utilization, in particular to a method for pretreatment and enzymolysis of corn straws.
Background
At present, agricultural and forestry wastes such as corn straws and the like are directly discarded, so that the environment is greatly polluted while resources are wasted; the small amount of the feed is used as animal feed, returned to the field or burnt to generate heat, and the utilization efficiency is low. Therefore, it is very necessary to improve the utilization efficiency of agricultural and forestry wastes such as corn stalks, and taking corn stalks as an example, the annual output is as high as 3.5 hundred million tons, which accounts for about 60% of the total straw output (wheat straws, rice straws, bean straws, cotton straws, corn straws and the like), and the development of the technology for processing and utilizing the corn stalks and other derived products to produce hemicellulose, xylose and the like has a far-reaching significance.
The conventional acid treatment method for preparing xylose uses common acid as a hydrolysis catalyst. The sulfuric acid is cheap, meets the requirement of industrial production, and has good hydrolysis effect, so the sulfuric acid is generally used in a large amount. When lignocellulose is hydrolyzed by acid, the glycosidic bond in the hemicellulose or cellulose is broken, so that the hemicellulose or cellulose is changed as follows: the average polymerization degree of the hemicellulose or cellulose is obviously reduced; the internal surface area of hemicellulose or cellulose increases and the crystallinity decreases; the protective layer of lignin is also destroyed, causing degradation of hemicellulose or cellulose. In lignocellulose acidolysis, hemicellulose is first broken down due to easier separation.
However, the traditional acid hydrolysis method requires a series of processes such as deacidification and neutralization in the production process, and has great pollution to the environment; meanwhile, the production process causes corrosion to equipment, and the economic investment is also large.
Disclosure of Invention
The invention aims to overcome the problems in the prior art and provides a method for pretreatment and enzymolysis of corn straws.
In order to achieve the technical purpose and achieve the technical effect, the invention is realized by the following technical scheme:
a method for pretreatment and enzymolysis of corn straws comprises the following steps:
(1) cutting corn stalks, and sequentially crushing, washing and drying to obtain particles;
(2) adding the particles obtained in the step (1) into a dilute sulfuric acid solution according to a certain solid-to-liquid ratio, pretreating for a period of time under the condition of supercritical carbon dioxide, filtering, collecting filtrate and filter residues, and drying the filter residues in an oven for a period of time to remove moisture to obtain a solid matter;
(3) and (3) taking the solid obtained in the step (2) as an enzyme hydrolysis substrate, adding xylanase and trisodium citrate buffer solution according to a certain solid-to-liquid ratio, and performing enzyme hydrolysis for a period of time to obtain xylose.
Further, according to the method for pretreating and enzymolyzing the corn stalks, in the step (1), the corn stalks are cut off and crushed into the granularity of 30-50 meshes.
Further, according to the method for pretreating and enzymolyzing the corn straws, in the step (2), the particles are added into a dilute sulfuric acid solution according to the solid-to-liquid ratio of 1:8-12, and H in the dilute sulfuric acid solution2SO4The mass percentage of the components is 1-2%.
Further, according to the method for the pretreatment and enzymolysis of the corn stalks, in the step (2), the pretreatment time is 30-240min under the condition of supercritical carbon dioxide.
Further, according to the method for pretreating and enzymolyzing the corn stalks, in the step (2), the temperature of pretreatment is 35-70 ℃ under the condition of supercritical carbon dioxide.
Further, according to the method for the pretreatment and the enzymolysis of the corn stalks, in the step (2), the drying temperature of the oven is 30-60 ℃, and the drying time is 10-14 hours.
Further, according to the method for pretreating and hydrolyzing the corn straws, in the step (2), the xylanase is acidic xylanase, and the enzyme activity is 200000U/g.
Further, in the method for pretreating and hydrolyzing corn stalks with enzyme, in the step (2), the dosage of the xylanase is 28000 and 33000U/g substrate, preferably 31250U/g substrate.
Further, according to the method for pretreating and hydrolyzing corn stalks, in the step (3), the pH of the trisodium citrate buffer solution is 5, and the xylanase and the trisodium citrate buffer solution are added according to the solid-to-liquid ratio of 1:40-60, preferably 1: 50.
Further, in the method for pretreating and hydrolyzing the corn stalks by the enzyme, in the step (3), the time for hydrolyzing the enzyme is 20 to 28 hours, preferably 24 hours.
The invention has the beneficial effects that:
the method of the invention has the advantages of simple operation,
the method disclosed by the invention is scientific and reasonable in design, and the effect of the supercritical carbon dioxide pretreatment is enhanced by using the dilute acid at a low temperature, so that the complex cross-linked structure of the lignocellulose is broken better, the chemical bond between the lignin and the hemicellulose is broken, the lignin is removed, more hemicellulose is exposed, and the enzymatic hydrolysis efficiency is improved. Compared with the traditional acid hydrolysis method, the method is environment-friendly and has low economic investment.
Of course, it is not necessary for any one product that embodies the invention to achieve all of the above advantages simultaneously.
Detailed Description
The technical solutions in the embodiments of the present invention will be clearly and completely described below, and it is obvious that the described embodiments are only a part of the embodiments of the present invention, and not all embodiments. All other embodiments, which can be derived by a person skilled in the art from the embodiments given herein without making any creative effort, shall fall within the protection scope of the present invention.
The following embodiments are relevant to the present invention:
example 1
Crushing corn straws, sieving the corn straws by using a 2mm sieve, taking 50g of the corn straws as a raw material for biomass pretreatment, adding the raw material into 500ml of 1% dilute sulfuric acid solution according to a solid-to-liquid ratio of 10%, reacting at 35 ℃ for 60min, after pretreatment, carrying out suction filtration by using a non-woven fabric, collecting filtrate and filter residue, washing the filter residue by using 1000m1 deionized water, and then carrying out HPLC analysis on the filtrate to evaluate the pretreatment effect; and drying the filter residue in an oven at 45 ℃ for 12 hours to remove water.
Taking 2g of the pretreated solid as an enzyme hydrolysis substrate, and carrying out enzyme hydrolysis by using acid xylanase (200000U/g of enzyme activity, Shandong Scotto Han Biotech Co., Ltd.), wherein the enzyme dosage is 0.625g (31250U/g substrate); 100ml of trisodium citrate buffer (pH 5) is added, the solid-to-liquid ratio is 1:50, and the enzymatic hydrolysis time is 24 h. Extracting 0.5ml of enzyme hydrolysate at 0, 1, 4, 8, 12, 24h, immediately putting into boiling water for 10min for inactivation after extraction, and centrifuging with a high speed centrifuge at 10000rpm for 10min after inactivation. After centrifugation, taking the supernatant for HPLC analysis, and quantifying the xylose content in the enzyme water solution. The final xylose yield per unit was calculated to be 15.43%, which is a large improvement compared to the 9.40% yield of the feedstock.
Example 2
Crushing corn straws, sieving the corn straws by using a 2mm sieve, taking 50g of the corn straws as a raw material for biomass pretreatment, adding the raw material into 500ml of 1% dilute sulfuric acid solution according to a solid-to-liquid ratio of 10%, reacting at 50 ℃ for 60min, after pretreatment, carrying out suction filtration by using a non-woven fabric, collecting filtrate and filter residue, washing the filter residue by using 1000m1 deionized water, and then carrying out HPLC analysis on the filtrate to evaluate the pretreatment effect; and drying the filter residue in an oven at 45 ℃ for 12 hours to remove water.
Taking 2g of the pretreated solid as an enzyme hydrolysis substrate, and carrying out enzyme hydrolysis by using acid xylanase (200000U/g of enzyme activity, Shandong Scotto Han Biotech Co., Ltd.), wherein the enzyme dosage is 0.625g (31250U/g substrate); 100ml of trisodium citrate buffer (pH 5) is added, the solid-to-liquid ratio is 1:50, and the enzymatic hydrolysis time is 24 h. Extracting 0.5ml of enzyme hydrolysate at 0, 1, 4, 8, 12, 24h, immediately putting into boiling water for 10min for inactivation after extraction, and centrifuging with a high speed centrifuge at 10000rpm for 10min after inactivation. After centrifugation, taking the supernatant for HPLC analysis, and quantifying the xylose content in the enzyme water solution. The final xylose yield was calculated to be 15.74% with a large improvement compared to the 9.40% yield of the feedstock.
Example 3
Crushing corn straws, sieving the corn straws by using a 2mm sieve, taking 50g of the corn straws as a raw material for biomass pretreatment, adding the raw material into 500ml of 1% dilute sulfuric acid solution according to a solid-to-liquid ratio of 10%, reacting at 70 ℃ for 60min, after pretreatment, carrying out suction filtration by using a non-woven fabric, collecting filtrate and filter residue, washing the filter residue by using 1000m1 deionized water, and then carrying out HPLC analysis on the filtrate to evaluate the pretreatment effect; and drying the filter residue in an oven at 45 ℃ for 12 hours to remove water.
Taking 2g of the pretreated solid as an enzyme hydrolysis substrate, and carrying out enzyme hydrolysis by using acid xylanase (200000U/g of enzyme activity, Shandong Scotto Han Biotech Co., Ltd.), wherein the enzyme dosage is 0.625g (31250U/g substrate); 100ml of trisodium citrate buffer (pH 5) is added, the solid-to-liquid ratio is 1:50, and the enzymatic hydrolysis time is 24 h. Extracting 0.5ml of enzyme hydrolysate at 0, 1, 4, 8, 12, 24h, immediately putting into boiling water for 10min for inactivation after extraction, and centrifuging with a high speed centrifuge at 10000rpm for 10min after inactivation. After centrifugation, taking the supernatant for HPLC analysis, and quantifying the xylose content in the enzyme water solution. The final xylose yield was calculated to be 28.51% with a large improvement compared to the 9.40% yield of the feedstock.
Example 4
Crushing corn straws, sieving the corn straws by using a 2mm sieve, taking 50g of the corn straws as a raw material for biomass pretreatment, adding the raw material into 500ml of 2% dilute sulfuric acid solution according to a solid-to-liquid ratio of 10%, reacting at 70 ℃ for 30min, after pretreatment, carrying out suction filtration by using a non-woven fabric, collecting filtrate and filter residue, washing the filter residue by using 1000m1 deionized water, and then carrying out HPLC analysis on the filtrate to evaluate the pretreatment effect; and drying the filter residue in an oven at 45 ℃ for 12 hours to remove water.
Taking 2g of the pretreated solid as an enzyme hydrolysis substrate, and carrying out enzyme hydrolysis by using acid xylanase (200000U/g of enzyme activity, Shandong Scotto Han Biotech Co., Ltd.), wherein the enzyme dosage is 0.625g (31250U/g substrate); 100ml of trisodium citrate buffer (pH 5) is added, the solid-to-liquid ratio is 1:50, and the enzymatic hydrolysis time is 24 h. Extracting 0.5ml of enzyme hydrolysate at 0, 1, 4, 8, 12, 24h, immediately putting into boiling water for 10min for inactivation after extraction, and centrifuging with a high speed centrifuge at 10000rpm for 10min after inactivation. After centrifugation, taking the supernatant for HPLC analysis, and quantifying the xylose content in the enzyme water solution. The final xylose yield per unit was calculated to be 24.82%, which is a large improvement compared to the 9.40% yield of the feedstock.
Example 5
Crushing corn straws, sieving the corn straws by using a 2mm sieve, taking 50g of the corn straws as a raw material for biomass pretreatment, adding the raw material into 500ml of 2% dilute sulfuric acid solution according to a solid-to-liquid ratio of 10%, reacting at 70 ℃ for 60min, after pretreatment, carrying out suction filtration by using a non-woven fabric, collecting filtrate and filter residue, washing the filter residue by using 1000m1 deionized water, and then carrying out HPLC analysis on the filtrate to evaluate the pretreatment effect; and drying the filter residue in an oven at 45 ℃ for 12 hours to remove water.
Taking 2g of the pretreated solid as an enzyme hydrolysis substrate, and carrying out enzyme hydrolysis by using acid xylanase (200000U/g of enzyme activity, Shandong Scotto Han Biotech Co., Ltd.), wherein the enzyme dosage is 0.625g (31250U/g substrate); 100ml of trisodium citrate buffer (pH 5) is added, the solid-to-liquid ratio is 1:50, and the enzymatic hydrolysis time is 24 h. Extracting 0.5ml of enzyme hydrolysate at 0, 1, 4, 8, 12, 24h, immediately putting into boiling water for 10min for inactivation after extraction, and centrifuging with a high speed centrifuge at 10000rpm for 10min after inactivation. After centrifugation, taking the supernatant for HPLC analysis, and quantifying the xylose content in the enzyme water solution. The final xylose yield was calculated to be 25.64% with a large improvement compared to the 9.40% yield of the feedstock.
Example 6
Crushing corn straws, sieving the corn straws by using a 2mm sieve, taking 50g of the corn straws as a raw material for biomass pretreatment, adding the raw material into 500ml of 2% dilute sulfuric acid solution according to a solid-to-liquid ratio of 10%, reacting at 70 ℃ for 120min, after pretreatment, carrying out suction filtration by using a non-woven fabric, collecting filtrate and filter residue, washing the filter residue by using 1000m1 deionized water, and then carrying out HPLC analysis on the filtrate to evaluate the pretreatment effect; and drying the filter residue in an oven at 45 ℃ for 12 hours to remove water.
Taking 2g of the pretreated solid as an enzyme hydrolysis substrate, and carrying out enzyme hydrolysis by using acid xylanase (200000U/g of enzyme activity, Shandong Scotto Han Biotech Co., Ltd.), wherein the enzyme dosage is 0.625g (31250U/g substrate); 100ml of trisodium citrate buffer (pH 5) is added, the solid-to-liquid ratio is 1:50, and the enzymatic hydrolysis time is 24 h. Extracting 0.5ml of enzyme hydrolysate at 0, 1, 4, 8, 12, 24h, immediately putting into boiling water for 10min for inactivation after extraction, and centrifuging with a high speed centrifuge at 10000rpm for 10min after inactivation. After centrifugation, taking the supernatant for HPLC analysis, and quantifying the xylose content in the enzyme water solution. The final xylose yield per unit was calculated to be 26.21%, which is a large improvement compared to the 9.40% yield of the feedstock.
Example 7
Crushing corn straws, sieving the corn straws by using a 2mm sieve, taking 50g of the corn straws as a raw material for biomass pretreatment, adding the raw material into 500ml of 2% dilute sulfuric acid solution according to a solid-to-liquid ratio of 10%, reacting at 70 ℃ for 240min, after pretreatment, carrying out suction filtration by using a non-woven fabric, collecting filtrate and filter residue, washing the filter residue by using 1000m1 deionized water, and then carrying out HPLC analysis on the filtrate to evaluate the pretreatment effect; and drying the filter residue in an oven at 45 ℃ for 12 hours to remove water.
Taking 2g of the pretreated solid as an enzyme hydrolysis substrate, and carrying out enzyme hydrolysis by using acid xylanase (200000U/g of enzyme activity, Shandong Scotto Han Biotech Co., Ltd.), wherein the enzyme dosage is 0.625g (31250U/g substrate); 100ml of trisodium citrate buffer (pH 5) is added, the solid-to-liquid ratio is 1:50, and the enzymatic hydrolysis time is 24 h. Extracting 0.5ml of enzyme hydrolysate at 0, 1, 4, 8, 12, 24h, immediately putting into boiling water for 10min for inactivation after extraction, and centrifuging with a high speed centrifuge at 10000rpm for 10min after inactivation. After centrifugation, taking the supernatant for HPLC analysis, and quantifying the xylose content in the enzyme water solution. The final xylose yield was calculated to be 30.85% with a large improvement compared to the 9.40% yield of the feedstock.
The preferred embodiments of the invention disclosed above are intended to be illustrative only. The preferred embodiments are not intended to be exhaustive or to limit the invention to the precise embodiments disclosed. Obviously, many modifications and variations are possible in light of the above teaching. The embodiments were chosen and described in order to best explain the principles of the invention and the practical application, to thereby enable others skilled in the art to best utilize the invention. The invention is limited only by the claims and their full scope and equivalents.

Claims (10)

1. A method for pretreatment and enzymolysis of corn straws is characterized by comprising the following steps:
(1) cutting corn stalks, and sequentially crushing, washing and drying to obtain particles;
(2) adding the particles obtained in the step (1) into a dilute sulfuric acid solution according to a certain solid-to-liquid ratio, pretreating for a period of time under the condition of supercritical carbon dioxide, filtering, collecting filtrate and filter residues, and drying the filter residues in an oven for a period of time to remove moisture to obtain a solid matter;
(3) and (3) taking the solid obtained in the step (2) as an enzyme hydrolysis substrate, adding xylanase and trisodium citrate buffer solution according to a certain solid-to-liquid ratio, and performing enzyme hydrolysis for a period of time to obtain xylose.
2. The method for pretreating and enzymolyzing corn stalks according to claim 1, wherein the method comprises the following steps: in the step (1), the corn straws are cut off and crushed into the granularity of 30-50 meshes.
3. The method for pretreating and enzymolyzing corn stalks according to claim 1, wherein the method comprises the following steps: in the step (2), the particles are added into a dilute sulfuric acid solution according to the solid-to-liquid ratio of 1:8-12, and H in the dilute sulfuric acid solution2SO4The mass percentage of the components is 1-2%.
4. The method for pretreating and enzymolyzing corn stalks according to claim 1, wherein the method comprises the following steps: in the step (2), the pretreatment time under the condition of supercritical carbon dioxide is 30-240 min.
5. The method for pretreating and enzymolyzing corn stalks according to claim 1, wherein the method comprises the following steps: in the step (2), the temperature of the pretreatment under the condition of supercritical carbon dioxide is 35-70 ℃.
6. The method for pretreating and enzymolyzing corn stalks according to claim 1, wherein the method comprises the following steps: in the step (2), the drying temperature of the oven is 30-60 ℃, and the drying time is 10-14 h.
7. The method for pretreating and enzymolyzing corn stalks according to claim 1, wherein the method comprises the following steps: in the step (2), the xylanase is acid xylanase, and the enzyme activity is 200000U/g.
8. The method for pretreating and enzymolyzing corn stalks according to claim 1, wherein the method comprises the following steps: in the step (2), the dosage of the xylanase is 28000 and 33000U/g substrate, preferably 31250U/g substrate.
9. The method for pretreating and enzymolyzing corn stalks according to claim 1, wherein the method comprises the following steps: in the step (3), the pH value of the trisodium citrate buffer solution is 5, and the xylanase and the trisodium citrate buffer solution are added according to the solid-to-liquid ratio of 1:40-60, preferably 1: 50.
10. The method for pretreating and enzymolyzing corn stalks according to claim 1, wherein the method comprises the following steps: in the step (3), the time for enzyme hydrolysis is 20-28h, preferably 24 h.
CN202011550711.8A 2020-12-24 2020-12-24 Pretreatment and enzymolysis method of corn straw Pending CN112553269A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN202011550711.8A CN112553269A (en) 2020-12-24 2020-12-24 Pretreatment and enzymolysis method of corn straw

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN202011550711.8A CN112553269A (en) 2020-12-24 2020-12-24 Pretreatment and enzymolysis method of corn straw

Publications (1)

Publication Number Publication Date
CN112553269A true CN112553269A (en) 2021-03-26

Family

ID=75033435

Family Applications (1)

Application Number Title Priority Date Filing Date
CN202011550711.8A Pending CN112553269A (en) 2020-12-24 2020-12-24 Pretreatment and enzymolysis method of corn straw

Country Status (1)

Country Link
CN (1) CN112553269A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN117681296A (en) * 2024-02-01 2024-03-12 山东埃尔派粉体科技股份有限公司 Pretreatment and superfine method for wood and bamboo raw materials

Citations (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN101434976A (en) * 2008-12-23 2009-05-20 中国石油化工股份有限公司 Novel method for saccharification of ligno-cellulose
CN101565725A (en) * 2009-06-02 2009-10-28 天津大学 Maize straw pretreatment method
CA2701407A1 (en) * 2009-04-23 2010-10-23 Greenfield Ethanol Inc. Fractionation of biomass for cellulosic ethanol and chemical production
CN104846024A (en) * 2015-06-03 2015-08-19 长春工业大学 Method for producing microbial oil by fermenting maize straw as raw material and esterifying microbial oil
CN105734086A (en) * 2014-12-08 2016-07-06 中国石油天然气股份有限公司 Pretreatment method of lignocellulose material and prepared lignocellulose
CN106701836A (en) * 2016-12-06 2017-05-24 北京利晟新能生物科技中心(有限合伙) Pretreatment method for preparation of biomass fuels by comprehensive utilization of all components of plant straw
CN107164424A (en) * 2017-07-12 2017-09-15 天津科技大学 It is a kind of to aoxidize the lignocellulose pretreatment method that delignification improves enzyme hydrolysis rate
CN108385421A (en) * 2018-04-08 2018-08-10 华南理工大学 Lignocellulosic supercritical CO2Explosion and its component separation method

Patent Citations (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN101434976A (en) * 2008-12-23 2009-05-20 中国石油化工股份有限公司 Novel method for saccharification of ligno-cellulose
CA2701407A1 (en) * 2009-04-23 2010-10-23 Greenfield Ethanol Inc. Fractionation of biomass for cellulosic ethanol and chemical production
CN101565725A (en) * 2009-06-02 2009-10-28 天津大学 Maize straw pretreatment method
CN105734086A (en) * 2014-12-08 2016-07-06 中国石油天然气股份有限公司 Pretreatment method of lignocellulose material and prepared lignocellulose
CN104846024A (en) * 2015-06-03 2015-08-19 长春工业大学 Method for producing microbial oil by fermenting maize straw as raw material and esterifying microbial oil
CN106701836A (en) * 2016-12-06 2017-05-24 北京利晟新能生物科技中心(有限合伙) Pretreatment method for preparation of biomass fuels by comprehensive utilization of all components of plant straw
CN107164424A (en) * 2017-07-12 2017-09-15 天津科技大学 It is a kind of to aoxidize the lignocellulose pretreatment method that delignification improves enzyme hydrolysis rate
CN108385421A (en) * 2018-04-08 2018-08-10 华南理工大学 Lignocellulosic supercritical CO2Explosion and its component separation method

Non-Patent Citations (3)

* Cited by examiner, † Cited by third party
Title
杨盛茹 等: "稀酸预处理玉米芯酶解工艺响应面优化研究", 《中国酿造》 *
袁丽婷: "玉米秸秆预处理技术研究进展", 《中国酿造》 *
郝刘丹 等: "木质纤维素的超临界二氧化碳预处理技术", 《应用科技》 *

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN117681296A (en) * 2024-02-01 2024-03-12 山东埃尔派粉体科技股份有限公司 Pretreatment and superfine method for wood and bamboo raw materials

Similar Documents

Publication Publication Date Title
CN101285106B (en) Process for preparing multicomponent liquid glucose and lignose while effectively hydrolyzing lignocellulosic biomass
CN106011199B (en) Pretreatment method of crop straws
CN102212976B (en) Method for separating bagasse cellulose from lignin
JP5322150B2 (en) Method for saccharification of biomass containing cellulose
CN108251472B (en) Preparation method of xylo-oligosaccharide
JP2009125050A (en) Pretreatment method for enzymatic hydrolysis of herbaceous biomass, ethanol production method using herbaceous biomass as raw material and ethanol production method using palm hollow bunch
CN100497647C (en) Method for adsorbing and decomposing stalk cellulose using cellulase
CN107164424A (en) It is a kind of to aoxidize the lignocellulose pretreatment method that delignification improves enzyme hydrolysis rate
CN105603021A (en) Method for enhancing tobacco stem enzymolysis effect by using surfactant
CN104762419A (en) Method for preparing xylooligosaccharide from corncobs through microwave-assisted hydrothermal treatment
CN111472186B (en) Method for preparing high-quality crop straw dissolving pulp through hydrothermal pretreatment
CN101153306B (en) Method for producing tangerine peel low methoxy group pectin by using pectinase
CN112553269A (en) Pretreatment and enzymolysis method of corn straw
CN110592292A (en) Pretreatment method for promoting biomass to efficiently extract xylose by mechanical method
CN106191168B (en) Method for preparing high-concentration fermentation sugar solution by using lignocellulose as raw material
CN106011181B (en) Method for preparing fuel ethanol from kitchen garbage
JP6213612B2 (en) Method for producing ethanol from lignocellulosic material
CN102181076B (en) Method for cleanly preparing starch containing abundant flavones and comprehensively utilizing radix puerariae resource
CN111909975A (en) Method for preparing functional oligosaccharide by microwave pretreatment oil tea fruit shell fermentation method
CN101665534B (en) Preparation method of concentrated protein of cottonseeds
JP6256967B2 (en) Pretreatment method for lignocellulose-containing biomass
CN104531806A (en) Method for producing fermentable sugar
CN105483184A (en) Production method of high-yield xylooligosaccharide
KR101584208B1 (en) Manufacturing method of xylose-rich xylan utilizing corn bran
CN107523596B (en) Method for realizing efficient enzymatic hydrolysis of biomass raw material and preparing fermentable sugar

Legal Events

Date Code Title Description
PB01 Publication
PB01 Publication
SE01 Entry into force of request for substantive examination
SE01 Entry into force of request for substantive examination
RJ01 Rejection of invention patent application after publication

Application publication date: 20210326

RJ01 Rejection of invention patent application after publication