CN115340682A - High-biological-activity lignin and preparation method thereof - Google Patents
High-biological-activity lignin and preparation method thereof Download PDFInfo
- Publication number
- CN115340682A CN115340682A CN202210925813.6A CN202210925813A CN115340682A CN 115340682 A CN115340682 A CN 115340682A CN 202210925813 A CN202210925813 A CN 202210925813A CN 115340682 A CN115340682 A CN 115340682A
- Authority
- CN
- China
- Prior art keywords
- lignin
- parts
- tio
- compound
- activity
- 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.)
- Granted
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08H—DERIVATIVES OF NATURAL MACROMOLECULAR COMPOUNDS
- C08H6/00—Macromolecular compounds derived from lignin, e.g. tannins, humic acids
Landscapes
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Biochemistry (AREA)
- Materials Engineering (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Cosmetics (AREA)
Abstract
The invention provides a method for preparing amination modified high-bioactivity lignin by using nano Lignin (LNP) as a raw material. The raw materials comprise 10-50 parts of nano lignin, 10-50 parts of amino compound, 10-50 parts of aldehyde compound and titanium dioxide (TiO) 2 ) 0.1 to 2 portions. Mixing lignin and amino compound in a certain proportion, magnetically stirring at normal temperature, and then mixing aldehyde compound and TiO 2 Water dispersion is evenly mixed in a dropwise adding mode, and Mannich reaction is carried out under the conditions of 60-100 ℃, inert gas protection and the like; the method has simple process, short preparation period and high yield. Compared with commercial antioxidants, the aminated modified high-activity lignin prepared from lignin has the advantages that the performance of scavenging free radicals is remarkably improved, and the aminated modified high-activity lignin has excellent synergistic ultraviolet shielding performance and antibacterial activity, and can be applied to the fields of cosmetics, personal care products, biopharmaceuticals, polymer composite materials and the like.
Description
Technical Field
The invention belongs to the field of environment-friendly natural high polymer materials, and relates to lignin with high oxidation resistance, broad-spectrum antibiosis and ultraviolet resistance and a preparation method thereof.
Background
With the improvement of quality of life, antioxidants play an increasingly important role in human dietary life. The addition of antioxidant functional substances such as dibutyl hydroxy toluene (BHT), tert-butyl p-hydroxy anisole (BHA), etc. can delay aging rate and promote health. Medical research shows that the primary generation of human chronic diseases is caused by the robbing of cell electrons, and free radicals enter a human body and then easily rob the cell electrons, so that the resistance of cells is reduced, the body is easily infected by germs, and even carcinogenic substances are formed. Therefore, the antioxidation and the elimination of free radicals are always the research hotspots at home and abroad.
With the increasing health awareness of people, the use of some natural antioxidants is gradually replacing commercial antioxidants, which is of great importance for reducing the cost and efficiently using the antioxidants. As a natural polyphenol polymer with a three-dimensional network structure, the lignin has quite diversified properties: such as oxidation resistance, antibiosis, innocuity, ultraviolet resistance, etc. However, currently most of the lignin is disposed of as industrial waste or fuel; and when the lignin is used as a natural antioxidant, the antioxidant and antibacterial activities of the lignin are low, and the ultraviolet shielding efficiency is not high enough. Therefore, the improvement of the comprehensive biological activity of the lignin has great significance for expanding the application of the lignin and promoting the sustainable utilization of resources. Documents Ind.Crops prod.2019,128,177-185, ACS Sustainable chem.Eng.2018,6 (2), 2591-2595 and Ind.Crops prod.2017,95,512-520 respectively improve the oxidation resistance of lignin through hydrothermal depolymerization, lacquer mold and ionic liquid modification, but the ultraviolet shielding performance and the antibacterial activity are not substantially improved; the document Green chem, 2020,22,6357-6371 reports that arginine, histidine and lysine are grafted onto the surface of lignin, so that the antibacterial activity of lignin is improved, the modified lignin product has selective antibacterial effect on gram-positive bacteria and gram-negative bacteria, but does not have broad-spectrum antibacterial function, and the antioxidant capacity and ultraviolet shielding capacity of lignin are not substantially improved.
Disclosure of Invention
In order to overcome the defects of the prior art, the invention provides a novel method for preparing lignin with excellent antioxidant, antibacterial and ultraviolet resistant functions by using a lignin two-step method. The invention can improve the specific surface area of lignin and increase antioxidant active groups. The prepared antioxidant nano lignin has excellent functions of antioxidation, synergistic broad-spectrum antibiosis, ultraviolet shielding and the like. The method has the advantages of simple synthesis process, easily obtained raw materials and environmental protection.
In order to achieve the purpose, the invention is realized by the following technical scheme:
the first object of the invention is a modified lignin and a preparation method thereof, which is characterized in that the modified lignin is prepared from raw materials comprising the following components:
in one embodiment of the invention, the components in the modification process comprise, by weight, 50 to 100 parts of nano lignin, 10 to 50 parts of an amino compound, 10 to 50 parts of an aldehyde compound, and TiO 2 0.1 to 2 portions.
In one embodiment of the invention, the modified lignin and the preparation method thereof are that 0.1-5 w/v% of nano lignin dispersion liquid and amino compound are mixed uniformly according to a certain proportion, and then aldehyde compound and TiO compound are added 2 And (3) uniformly mixing the dispersion liquid, reacting under the protection of inert gas, and dialyzing after the reaction is finished to obtain the modified lignin.
In one embodiment of the invention, the nano lignin is one or more of alkali lignin, organic solvent lignin, lignosulfonate and kraft lignin.
In one embodiment of the present invention, the aldehyde is one of formaldehyde, acetaldehyde, propionaldehyde, benzaldehyde, furfural, dialdehyde, and unsaturated aldehyde.
In one embodiment of the invention, the straight or branched alkyl amine has a carbon number of 1 to 8.
In one embodiment of the present invention, the amine is one of linear or branched alkylamine, cyclic amine, polyamine, hydroxyalkylamine, and amino acid.
In one embodiment of the invention, the aldehyde compound and TiO are slowly added dropwise at 60-100 deg.C 2 And (3) dispersing the mixture.
In one embodiment of the invention, the nano lignin dispersion and TiO 2 The solvent of the dispersion is water. In one embodiment of the present invention, the TiO is 2 The dosage is 0.1 to 2 parts
In one embodiment of the invention, the dialysis time is 1 to 12 hours.
In one embodiment of the invention, the nano-lignin and amine-based compound are added to a bottle, N 2 As protective gas, aldehyde compound and TiO are slowly dropped at 60-100 DEG C 2 And (3) carrying out Mannich reaction in a compounding way, and dialyzing after the reaction is finished for 1-12h to obtain the aminated modified lignin. The obtained product has excellent oxidation resistance, antibacterial and ultraviolet shielding functions
In one embodiment of the invention, the Mannich reaction is carried out under heated conditions, preferably under anhydrous conditions at from 50 to 100 ℃.
In one embodiment of the present invention, the required amount of the aldehydes and amines is 1.4 to 2.5 in terms of molar ratio of CHO to NH.
In one embodiment of the present invention, the aldehyde may be, but is not limited to, one of formaldehyde, acetaldehyde, propionaldehyde, benzaldehyde, furfural, dialdehyde (such as glutaraldehyde, glyoxal, etc.), unsaturated aldehyde (such as acrolein, crotonaldehyde, etc.).
In one embodiment of the present invention, the amine is one of linear or branched alkylamine, cyclic amine, polyamine (such as ethylenediamine, hexamethylenediamine, diethyltriamine, triethylenetetramine, and tetraethylpentamine), hydroxyalkylamine (such as hydroxyethylprimary amine, dihydroxyethylamine, triethanolamine, and aminoethylethanolamine), and amino acid (such as lysine, sarcosine, glycine, iminodiacetic acid, tyrosine, and aspartic acid).
In one embodiment of the present invention, the solvent may be at least one of water, acetone, dimethylformamide (DMF), dimethylacetamide (DMAC), tetrahydrofuran (THF), and dioxane.
The invention also provides modified lignin by utilizing the method.
The second purpose of the invention is to provide the application of the modified lignin in the fields of cosmetics, personal care products, biomedicine, coatings and polymer composite materials.
Compared with the prior art, the invention has the following advantages and beneficial effects:
1. the lignin raw material provided by the invention is wide in source, renewable, environment-friendly and biodegradable, and low in cost. Meanwhile, the surface of the nano lignin is high in activity, and compared with a commercial antioxidant, the aminated modified nano lignin disclosed by the invention is more excellent in environmental friendliness; the antioxidant has excellent antioxidant performance, the capacity of scavenging free radicals of Diphenyl Picryl Phenylhydrazine (DPPH) after 6 hours reaches 98.0%, and the effect is superior to that of a commercial antioxidant dibutyl hydroxy toluene (BHT).
2. The aminated lignin disclosed by the invention is safe and nontoxic, has excellent antibacterial performance, and the bacteriostatic efficiency of gram-positive bacteria and gram-negative bacteria exceeds 50% and exceeds the bacteriostatic efficiency of lignin per se (20%).
3. The T-LNP has a more excellent ultraviolet shielding function, and compared with lignin, the ultraviolet shielding performance is improved by more than 35%.
4. The modified T-LNP of the invention can be used in the fields of cosmetics, personal care products, biopharmaceuticals, polymer composites and the like.
Detailed Description
Although the present invention has been described in detail, the present invention is not limited thereto, and those skilled in the art can modify the principle of the present invention, and therefore, various modifications made in accordance with the principle of the present invention should be understood to fall within the scope of the present invention.
And (3) testing antioxidant activity: preparing a sample to be detected into a 0.01g/mL aqueous solution, mixing 2.0mL of the 0.01g/mL solution with 2.0mL of a 50mg/L DPPH solution, carrying out free radical capture reaction for 1, 3 and 6 hours, detecting and fitting a peak area at 517nm by using an ultraviolet spectrophotometer, and calculating to obtain the intensity of the removed free radicals, wherein the peak area of a blank sample at 517nm is 22.5.
And (3) testing the bacteriostatic activity: preparing the obtained lignin sample to 1.0g/L concentration, mixing 10 μ L with 180 μ L of bacterial suspension, spreading the mixture on agar plate of culture medium, irradiating with ultraviolet light at 37 deg.C for 3 hr, culturing in culture medium for 24 hr, observing and counting bacterial colony number, wherein the bacterial colony number of the lignin-free blank gram-positive bacteria (Staphylococcus aureus) and gram-negative bacteria (Escherichia coli) is 1.5 × 10 7 CFU/mL and 1.3X 10 7 CFU/mL。
And (3) testing ultraviolet shielding performance: and (2) fully mixing the obtained lignin sample with PVA in an aqueous solution, casting to form a film, wherein the lignin content is 1.0%, the film thickness is 200 micrometers, and testing the transparency (500 nm) and the ultraviolet shielding performance (320 nm) of the PVA composite material film by using an ultraviolet spectrophotometer, wherein the light transmittances of the pure PVA film at 500nm and 320nm are respectively 92% and 85%.
With respect to TiO 2 Dispersion liquid: 1.0g of TiO was taken 2 Dispersed in 100mL of water to prepare 0.01g/mL of TiO 2 The dispersion was prepared in one portion of 1.0mL of the dispersion.
Regarding the ZnO dispersion: 1.0g of ZnO was taken and dispersed in 100mL of water to prepare 0.01g/mL of ZnO dispersion, and 1.0mL of the dispersion was used as one portion.
Example 1:
adding nano lignin (100 parts by mass, 0.01 g) and ethylenediamine (10 parts) into a reaction flask, N 2 As protective gas, formaldehyde (10 parts) and TiO are slowly added dropwise at 60 DEG C 2 Performing Mannich reaction on the dispersion (0.1 part), and dialyzing after 10h reaction to obtain aminated modified lignin, wherein the product is T-LNP1 for short, and the antioxidant activity, the antibacterial activity and the ultraviolet shielding performance of the aminated modified lignin are shown in the table 1, the antibacterial activity and the ultraviolet shielding performance are shown in the table 2 and 3 respectively.
Example 2:
adding nano lignin (100 parts) and ethylenediamine (50 parts) into the mixtureIn a reaction flask, N 2 As protective gas, formaldehyde (50 parts) and TiO were slowly added dropwise at 100 deg.C 2 Performing Mannich reaction on the dispersion (0.5 part) and dialyzing after 1h reaction to obtain aminated modified lignin, wherein the product is T-LNP2 for short, and the antioxidant activity, the antibacterial activity and the ultraviolet shielding performance of the aminated modified lignin are shown in the table 1, the antibacterial activity and the ultraviolet shielding performance of the aminated modified lignin are shown in the table 2 and 3 respectively.
Example 3:
adding nano lignin (100 parts) and dihydroxyethylamine (50 parts) into a reaction flask, N 2 As protective gas, glutaraldehyde (50 parts) and TiO were slowly added dropwise at 100 ℃ 2 Performing Mannich reaction on the dispersion liquid (2 parts), and dialyzing after 1h reaction to obtain aminated modified lignin, wherein a product is T-LNP3 for short, and the antioxidant activity, the bacteriostatic activity and the ultraviolet shielding performance of the aminated modified lignin are shown in the table 1, the bacteriostatic activity and the ultraviolet shielding performance are shown in the table 2 and 3 respectively.
Example 4:
adding nano lignin (100 parts) and lysine (10 parts) into a reaction bottle, and adding N 2 As protective gas, formaldehyde (10 parts) and TiO are slowly added dropwise at 60 DEG C 2 Performing Mannich reaction on the dispersion (0.5 part), dialyzing after 12h reaction to obtain aminated modified lignin, wherein a product is T-LNP4 for short, and the antioxidant activity, the antibacterial activity and the ultraviolet shielding performance of the aminated modified lignin are shown in the table 1, the antibacterial activity and the ultraviolet shielding performance are shown in the table 2 and 3 respectively.
Example 5:
adding nano lignin (80 parts) and hexamethylene diamine (20 parts) into a reaction bottle, and adding N 2 As protective gas, furfural (20 parts) and TiO were slowly dropped at 70 deg.C 2 And (3) carrying out Mannich reaction on the dispersion liquid (1 part), and dialyzing after 8h of reaction to obtain aminated modified lignin, wherein a product is T-LNP5 for short, and the antioxidant activity, the antibacterial activity and the ultraviolet shielding performance of the aminated modified lignin are shown in the table 1 and the antibacterial activity and the ultraviolet shielding performance of the aminated modified lignin are shown in the table 2 and 3 respectively.
Example 6:
adding nano lignin (50 parts) and aspartic acid (50 parts) into a reaction bottle, N 2 As protective gas, acrolein (50 parts) and TiO were slowly added dropwise at 100 ℃ 2 Performing Mannich reaction on the dispersion liquid (2 parts), and dialyzing after 6h of reaction to obtain aminated modified lignin, wherein the product is called as a product for shortThe antioxidant activity, the bacteriostatic activity and the ultraviolet shielding performance of the T-LNP6 are shown in a table 1 and a table 2 and a table 3 respectively.
Example 7:
adding nano lignin (100 parts) and aspartic acid (25 parts) into a reaction bottle, N 2 As protective gas, acrolein (25 parts) and TiO were slowly added dropwise at 65 ℃ 2 Performing Mannich reaction on the dispersion liquid (1 part), and dialyzing after 12h reaction to obtain aminated modified lignin, wherein a product is T-LNP7 for short, and the antioxidant activity, the bacteriostatic activity and the ultraviolet shielding performance of the aminated modified lignin are shown in the table 1, the bacteriostatic activity and the ultraviolet shielding performance are shown in the table 2 and 3 respectively.
Example 8:
adding nano lignin (100 parts) and tyrosine (25 parts) into a reaction bottle, N 2 As protective gas, formaldehyde (25 parts) and TiO were slowly added dropwise at 100 deg.C 2 Performing Mannich reaction on the dispersion (1.5 parts) for 2 hours, and dialyzing after the reaction is finished to obtain aminated modified lignin, wherein a product is T-LNP8 for short, and the antioxidant activity, the bacteriostatic activity and the ultraviolet shielding performance of the aminated modified lignin are shown in the table 1, the bacteriostatic activity and the ultraviolet shielding performance are shown in the table 2 and 3 respectively.
Comparative example 1:
100 parts of common lignin is taken, acidolysis nanocrystallization and amination modification treatment are not carried out on the common lignin, only the raw material is ground, and the micrometer lignin is obtained by a 120-mesh screen, wherein the antioxidant activity, the bacteriostatic activity and the ultraviolet shielding performance of the micrometer lignin are shown in the table 1 and the table 2 respectively.
Comparative example 2:
adding nano lignin (100 parts, 0.01g in one part) into a reaction bottle, and slowly dripping TiO at 60 DEG C 2 After the dispersion (0.1 part) was completed, dialysis was performed to obtain comparative sample 2, whose antioxidant activity, bacteriostatic activity and ultraviolet shielding property are shown in tables 1, 2 and 3, respectively.
Comparative example 3:
referring to comparative example 2, tiO 2 The dispersion was replaced with an equivalent amount of ZnO dispersion, and the other was not changed to prepare a comparative sample 3, whose antioxidant activity is shown in table 1, antibacterial activity is shown in table 2, and ultraviolet shielding property is shown in table 3.
Comparative example 4:
100 parts of a commercial antioxidant BHT (dibutylhydroxytoluene) purchased from Merlan corporation was used as a comparative sample 4, and its antioxidant activity, bacteriostatic activity and ultraviolet shielding performance are shown in tables 1, 2 and 3, respectively.
Comparative example 5:
the aminated modified lignin was prepared by taking 100 parts of ordinary lignin and preparing the aminated modified lignin under the conditions of example 1, and comparative sample 5 was prepared, the antioxidant activity of which is shown in table 1, the bacteriostatic activity of which is shown in table 2, and the ultraviolet shielding property of which is shown in table 3.
Comparative example 6:
referring to example 1, tiO 2 The dispersion liquid is changed into an equivalent ZnO dispersion liquid, the other conditions are not changed, a comparison sample 6 is prepared, the antioxidant activity, the bacteriostatic activity and the ultraviolet shielding performance of the prepared aminated modified lignin are shown in a table 1, a table 2 and a table 3 respectively.
Comparative example 7:
with reference to example 1, no TiO was added 2 Comparison sample 7 of aminated modified lignin was prepared, and its antioxidant activity, bacteriostatic activity and ultraviolet screening properties are shown in tables 1, 2 and 3, respectively.
TABLE 1 comparison table of antioxidant activity of each sample
Description of the drawings: antioxidant efficiency Q 1 = (22.5-x)/22.5, x represents fitted area at 517nm of ultraviolet spectrophotometer at different times;
according to the above test results: compared with the comparative examples 1 and 2, the oxidation resistance of the examples 1 to 8 in different time periods is obviously improved; compared with the comparative example 3, the oxidation resistance of the examples 1 to 8 is even higher than that of the commercial antioxidant BHT after the radical capture reaction is carried out for 3 hours, because the Mannich reaction can not only increase the phenolic hydroxyl content of lignin, but also the generated amine groups enable the lignin to form more stable phenoxy free radicals, hydrogen protons can be more easily separated to react with DPPH radicals, and the oxidation resistance is improved; nano-lignin is more active than micro-lignin because of the increased specific surface area of small size lignin and more phenolic hydroxyl groups exposed. In contrast, comparative example 4, which did not treat lignin, had a small specific surface area, a low degree of amination reaction, and an antioxidant activity that was not as effective as the commercial antioxidant BHT.
TABLE 2 comparison table of bacteriostatic effect of each sample
Description of the invention: bacteriostatic efficiency Q 2 = (a-y)/a or = (b-y)/b, wherein a =1.5 × 10 7 CFU/mL；b＝1.3×10 7 CFU/mL, y represents the number of bacteria in different samples;
according to the above test results: compared with comparative examples 1, 2, 3 and 4, the bacteriostatic efficiency of examples 1 to 8 is obviously improved and exceeds 30 percent; compared with the comparative example 1, the nano lignin of the comparative example 2 has slightly improved bacteriostatic efficiency, the bacteriostatic efficiency of staphylococcus aureus is 20.0%, the bacteriostatic efficiency of escherichia coli is 13.8%, the antibacterial and antioxidant mechanisms of lignin are similar, namely the antioxidant performance is improved, the general antibacterial activity is improved to a certain extent, the nano lignin with small particle size can effectively inhibit the bacterial growth, BHT (example 3) also has certain antibacterial performance, the bacteriostatic efficiency of staphylococcus aureus is 24.0%, and the bacteriostatic efficiency of escherichia coli is 16.9%. Compared with comparative example 1, the amination modified lignin of comparative example 4 has obviously improved bacteriostatic efficiency, but is still at a lower level because the lignin used in comparative example 4 has large size and small specific surface area, so that amination reaction can not graft more amine groups on the lignin.
Also, in various embodiments, with TiO 2 The principle of the method lies in that titanium dioxide decomposes bacteria under the action of photocatalysis to achieve antibacterial effect, aminated lignin and titanium dioxide show synergistic antibacterial effect, for example, in example 6, the antibacterial efficiency of staphylococcus aureus of the prepared modified lignin reaches 93.3%, the antibacterial efficiency of escherichia coli bacteria reaches 93.1%, which exceeds the antibacterial efficiency of all other samples. The experimental results show that the compound is reacted with TiO 2 The product obtained by Mannich reaction after compounding shows the synergistic broad-spectrum antibacterial effect of ultraviolet light catalysis.
TABLE 3 ultraviolet and visible light transmittance of PVA composite films of each component
| Test specimen | 320nm transmittance (%) | 500nm transmittance (%) |
| Example 1 | 6.5 | 70.4 |
| Example 2 | 3.6 | 70.8 |
| Example 3 | 1.5 | 73.5 |
| Example 4 | 4.6 | 65.6 |
| Example 5 | 2.5 | 69.2 |
| Example 6 | 1.0 | 71.5 |
| Example 7 | 3.4 | 68.2 |
| Example 8 | 2.4 | 72.1 |
| Comparative example 1 | 30.2 | 82.4 |
| Comparative example 2 | 10.4 | 83.1 |
| Comparative example 3 | 78.3 | 84.6 |
| Comparative example 4 | 80.4 | 92.0 |
| Comparative example 5 | 20.6 | 60.4 |
| Comparative example 6 | 77.4 | 88.3 |
| Comparative example 7 | 15.8 | 66.6 |
According to the above test results: compared with comparative examples 1, 2, 3 and 4, the ultraviolet shielding performance of examples 1 to 8 is obviously improved, but certain transparent performance is sacrificed; also in each of examples and comparative example 5, with TiO 2 The content is increased, the light transparency is improved, and the ultraviolet shielding performance is further improved. Compared with the comparative example 1, the ultraviolet shielding capability of the nano lignin in the comparative example 2 is higher, because the nano lignin with small particle size can be uniformly distributed in PVA, and the ultraviolet shielding performance is improved; meanwhile, BHT is colorless and transparent after being dissolved in water, so that the uvioresistant performance of the PVA film is not improved; comparative example 4 the aminated modified lignin showed a decrease in the ultraviolet transmittance to 20.6%, but also in the visible light transmittance after the amination to 60.4%; by reaction with TiO 2 The ultraviolet shielding capability of the product obtained by Mannich amination modification after compounding is further improved, in example 6, the ultraviolet shielding performance at 320nm reaches 99.0%, and the light transparency at 500nm is kept at a level of 72.1%, so that the product has higher optical transparency and excellent ultraviolet shielding function, and compared with the example, the ultraviolet shielding performance is improved by more than 35%.
In conclusion, the lignin with high oxidation resistance, antibacterial property and ultraviolet resistance prepared by the invention can be used in the fields of cosmetics, personal care products, biopharmaceuticals, polymer-based composite materials and the like.
Claims (10)
1. The method for preparing the modified lignin is characterized in that the method is implemented by an amine compound, an aldehyde compound and TiO 2 Modifying the nano lignin.
2. The method of claim 1, wherein the components in the modification process comprise, by weight, 50 to 100 parts of nano lignin, 10 to 50 parts of an amino compound, 10 to 50 parts of an aldehyde compound, and 0.1 to 2 parts of TiO 2 。
3. According to the rightThe method of claim 1, wherein the method comprises mixing 0.1-5 w/v% of the nano lignin dispersion with the amino compound, and then adding the aldehyde compound and the TiO 2 And (3) uniformly mixing the dispersion liquid, reacting under the protection of inert gas, and dialyzing after the reaction is finished to obtain the modified lignin.
4. The method of claim 1, wherein the nano lignin is one or more of alkali lignin, organosolv lignin, lignosulfonate, and kraft lignin.
5. The method of claim 1, wherein the aldehyde is one of formaldehyde, acetaldehyde, propionaldehyde, benzaldehyde, furfural, dialdehyde, and unsaturated aldehyde.
6. The method of claim 1, wherein the amine is one of a linear or branched alkylamine, a cyclic amine, a polyamine, a hydroxyalkylamine, and an amino acid.
7. The method as claimed in claim 3, wherein the aldehyde compound and TiO are slowly added dropwise at 60-100 ℃ 2 And (3) dispersing the mixture.
8. The method according to any one of claims 1 to 7, wherein the amount of the aldehyde compound and the amine compound is 1.4 to 2.5 in terms of molar ratio of CHO to NH.
9. A modified lignin prepared by the method of any one of claims 1 to 8.
10. Use of a modified lignin according to claim 9 in the fields of cosmetics, personal care products, biopharmaceuticals, coatings, polymer composites.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN2021109014245 | 2021-08-06 | ||
| CN202110901424.5A CN113698623A (en) | 2021-08-06 | 2021-08-06 | High-biological-activity lignin and preparation method thereof |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| CN115340682A true CN115340682A (en) | 2022-11-15 |
| CN115340682B CN115340682B (en) | 2023-08-25 |
Family
ID=78651715
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CN202110901424.5A Withdrawn CN113698623A (en) | 2021-08-06 | 2021-08-06 | High-biological-activity lignin and preparation method thereof |
| CN202210925813.6A Active CN115340682B (en) | 2021-08-06 | 2022-08-03 | High-bioactivity lignin and preparation method thereof |
Family Applications Before (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CN202110901424.5A Withdrawn CN113698623A (en) | 2021-08-06 | 2021-08-06 | High-biological-activity lignin and preparation method thereof |
Country Status (1)
| Country | Link |
|---|---|
| CN (2) | CN113698623A (en) |
Families Citing this family (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN114982784B (en) * | 2022-05-24 | 2023-05-16 | 雅思汀娜（北京）科技有限公司 | Modified lignin antibacterial agent and antibacterial agent composition containing same |
| CN115350111B (en) * | 2022-07-26 | 2023-10-20 | 华南理工大学 | Lignin-based stimulus-responsive long-acting broad-spectrum ultraviolet-resistant protective material and preparation and application thereof |
| CN115216026B (en) * | 2022-08-15 | 2023-05-26 | 齐鲁工业大学 | Method for preparing low-color nano lignin |
| CN116239792B (en) * | 2023-02-15 | 2024-04-23 | 广东省科学院微生物研究所(广东省微生物分析检测中心) | Medium-chain amino lignin antibacterial agent and preparation method and application thereof |
Citations (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH0268128A (en) * | 1988-08-30 | 1990-03-07 | Westvaco Corp | Surfactant |
| US20130180927A1 (en) * | 2012-01-13 | 2013-07-18 | General Electric Company | Formaldehyde-free lignin-amine coagulants |
| US20150135989A1 (en) * | 2013-11-21 | 2015-05-21 | Empire Technology Development Llc | Zwitterionic lignin derivatives |
| CN109988317A (en) * | 2019-03-20 | 2019-07-09 | 华南理工大学 | A kind of amino-acid modified lignin broad spectrum antimicrobial agent and the preparation method and application thereof |
Family Cites Families (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN109482168B (en) * | 2018-11-19 | 2020-05-22 | 华南理工大学 | Lignin carbon/nano titanium dioxide composite photocatalyst and preparation method and application thereof |
| CN113004557A (en) * | 2021-02-26 | 2021-06-22 | 江南大学 | Intrinsic ultraviolet shielding polyurethane lignin composite film and preparation method thereof |
-
2021
- 2021-08-06 CN CN202110901424.5A patent/CN113698623A/en not_active Withdrawn
-
2022
- 2022-08-03 CN CN202210925813.6A patent/CN115340682B/en active Active
Patent Citations (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH0268128A (en) * | 1988-08-30 | 1990-03-07 | Westvaco Corp | Surfactant |
| US20130180927A1 (en) * | 2012-01-13 | 2013-07-18 | General Electric Company | Formaldehyde-free lignin-amine coagulants |
| US20150135989A1 (en) * | 2013-11-21 | 2015-05-21 | Empire Technology Development Llc | Zwitterionic lignin derivatives |
| CN109988317A (en) * | 2019-03-20 | 2019-07-09 | 华南理工大学 | A kind of amino-acid modified lignin broad spectrum antimicrobial agent and the preparation method and application thereof |
Non-Patent Citations (2)
| Title |
|---|
| SAMB-JOSHI, K.M.: "《Lignin-mediated biosynthesis of ZnO and TiO2 nanocomposites for enhanced antimicrobial activity》", 《JOURNAL OF COMPOSITES SCIENCE》 * |
| YANG WEIJUN: "《Enhancing the Radical Scavenging Activity and UV Resistance of Lignin Nanoparticles via Surface Mannich Amination toward a Biobased Antioxidant》", 《BIOMACROMOLECULES》 * |
Also Published As
| Publication number | Publication date |
|---|---|
| CN113698623A (en) | 2021-11-26 |
| CN115340682B (en) | 2023-08-25 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| CN115340682A (en) | High-biological-activity lignin and preparation method thereof | |
| Kaya et al. | New chitin, chitosan, and O-carboxymethyl chitosan sources from resting eggs of Daphnia longispina (Crustacea); with physicochemical characterization, and antimicrobial and antioxidant activities | |
| CN108822838B (en) | Preparation method and application of copper-doped carbon quantum dots | |
| CN111328918B (en) | Preparation method of attapulgite-based pH response antibacterial material | |
| CN107434305B (en) | Water purifying agent with defect-rich carbon carrier immobilized microorganisms and preparation method thereof | |
| CN110818955B (en) | MOF (Metal organic framework) proanthocyanidin-loaded antibacterial film and preparation method thereof | |
| CN111011393A (en) | Preparation of simulated oxidase and photocatalytic bacteriostatic and bactericidal application thereof | |
| CN109702218B (en) | Method for preparing nano-silver particles by using phyllanthus emblica extract, product and application | |
| Oh et al. | Synthesis and antibacterial activity of versatile substrate‐coated biocidal material via catechol chemistry | |
| CN113025318A (en) | Carbon quantum dot using pepper as carbon source and preparation method and application thereof | |
| CN110558329B (en) | Diphenylalanine/g-C3N4Antibacterial agent and preparation method and application thereof | |
| KR100949719B1 (en) | Antibacterial zeolite resin composition | |
| CN107446143B (en) | Silver ion antibacterial liquid, silver ion antibacterial gel and preparation method thereof | |
| Neethidevan et al. | Wattakaka volubilis powered green synthesized CuO, NiO and ZnO nanoparticles for cost-effective biomedical applications | |
| CN115245176A (en) | Synthetic method for preparing antibacterial agent containing nano silver powder and having antibacterial property | |
| CN114957748A (en) | Antibacterial food packaging film and preparation method thereof | |
| CN104120095A (en) | Streptomyces albus and application thereof | |
| CN110229249B (en) | Preparation method of quaternized chitosan-carboxyl-terminated xanthone composite antibacterial material | |
| CN112674124A (en) | Environment-friendly biomass antibacterial insect repellent and preparation method thereof | |
| CN111109272A (en) | Bio-based antibacterial agent and application thereof | |
| CN111643705A (en) | Essential oil composition and application thereof in preparation of air freshener | |
| CN112219867A (en) | Metal particle reinforced titanium dioxide antibacterial composite | |
| CN110551290B (en) | Slow-release antibacterial molecular cluster resin and preparation method and application thereof | |
| Zhang et al. | Acrylic thiazole copolymer microspheres with “cluster effect” for long‐lasting antimicrobial activity and plant growth promotion | |
| CN111117908A (en) | Bacillus amyloliquefaciens Ba0002 and application thereof |
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 | ||
| GR01 | Patent grant | ||
| GR01 | Patent grant |