CN116333832A - Antifogging cleaning glasses wet tissue and production process thereof - Google Patents

Antifogging cleaning glasses wet tissue and production process thereof Download PDF

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CN116333832A
CN116333832A CN202310312971.9A CN202310312971A CN116333832A CN 116333832 A CN116333832 A CN 116333832A CN 202310312971 A CN202310312971 A CN 202310312971A CN 116333832 A CN116333832 A CN 116333832A
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fog
chitosan
substrate
cleaning
cleaning solution
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薛浩锴
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Jiangyin Yunzhi Medical Non Woven Products Co ltd
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Jiangyin Yunzhi Medical Non Woven Products Co ltd
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    • GPHYSICS
    • G02OPTICS
    • G02CSPECTACLES; SUNGLASSES OR GOGGLES INSOFAR AS THEY HAVE THE SAME FEATURES AS SPECTACLES; CONTACT LENSES
    • G02C13/00Assembling; Repairing; Cleaning
    • G02C13/006Devices specially adapted for cleaning spectacles frame or lenses
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D1/00Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
    • C11D1/88Ampholytes; Electroneutral compounds
    • C11D1/92Sulfobetaines ; Sulfitobetaines
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D3/00Other compounding ingredients of detergent compositions covered in group C11D1/00
    • C11D3/0005Other compounding ingredients characterised by their effect
    • C11D3/0078Compositions for cleaning contact lenses, spectacles or lenses
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D3/00Other compounding ingredients of detergent compositions covered in group C11D1/00
    • C11D3/16Organic compounds
    • C11D3/20Organic compounds containing oxygen
    • C11D3/2003Alcohols; Phenols
    • C11D3/2006Monohydric alcohols
    • C11D3/201Monohydric alcohols linear
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D3/00Other compounding ingredients of detergent compositions covered in group C11D1/00
    • C11D3/16Organic compounds
    • C11D3/20Organic compounds containing oxygen
    • C11D3/2003Alcohols; Phenols
    • C11D3/2065Polyhydric alcohols
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D3/00Other compounding ingredients of detergent compositions covered in group C11D1/00
    • C11D3/16Organic compounds
    • C11D3/20Organic compounds containing oxygen
    • C11D3/22Carbohydrates or derivatives thereof
    • C11D3/222Natural or synthetic polysaccharides, e.g. cellulose, starch, gum, alginic acid or cyclodextrin
    • 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
    • Y02P20/55Design of synthesis routes, e.g. reducing the use of auxiliary or protecting groups

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  • Chemical & Material Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Wood Science & Technology (AREA)
  • Health & Medical Sciences (AREA)
  • Organic Chemistry (AREA)
  • Engineering & Computer Science (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Emergency Medicine (AREA)
  • Physics & Mathematics (AREA)
  • Optics & Photonics (AREA)
  • Ophthalmology & Optometry (AREA)
  • Molecular Biology (AREA)
  • General Physics & Mathematics (AREA)
  • Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
  • Detergent Compositions (AREA)

Abstract

The invention relates to the technical field of anti-fog cleaning products, in particular to an anti-fog cleaning glasses wet tissue and a production process thereof. The anti-fog cleaning glasses wet tissue comprises a substrate and an anti-fog cleaning solution added to the substrate, wherein the anti-fog cleaning solution comprises the following raw materials in percentage by mass: 4-10% of modified chitosan, 10-15% of alginate, 5-8% of amphoteric surfactant, 2-5% of glycerol, 30-40% of absolute ethyl alcohol and the balance of deionized water. According to the novel antifogging cleaning glasses wet tissue, the chitosan is modified to have wide solubility, and the amino retention in the modified chitosan is controlled to be compounded with the alginate and the amphoteric surfactant, so that the problem that the antifogging duration is short due to the fact that the surfactant molecules are easy to migrate is solved.

Description

Antifogging cleaning glasses wet tissue and production process thereof
Technical Field
The invention relates to the technical field of anti-fog cleaning products, in particular to an anti-fog cleaning glasses wet tissue and a production process thereof.
Background
People often encounter the following two problems in using glasses: firstly, dirt such as dust, fingerprints and oil stains is inevitably stuck on the lens in the using process, if the lens is not cleaned, the optical performance and imaging quality of the lens are affected, and the vision of a user is damaged to a certain extent, so that the lens is required to be cleaned frequently to keep the cleanliness and the light transmittance; secondly, many lenses have poor anti-fog properties, and when entering a high-temperature environment from a low-temperature environment or when being covered by a nose with a mask in winter, hot air sprayed out of the nose can condense on the lenses when encountering cold lenses, so that the lenses are invisible and dangerous to people driving vehicles.
For the problem of unsatisfactory antifogging effect of the lens, the current antifogging measure for the lens mainly comprises hydrophilic antifogging, namely, a layer of hydrophilic substance is coated on the surface of the lens, so that water drops spread rapidly on the surface of the lens to form a water film, and the antifogging aim is achieved. Wherein the surfactant is the hydrophilic substance most used as an anti-fog means, and when the surfactant is used for anti-fog protection of the lens, two interfaces, namely a film-water interface and a water-air interface, are formed on the surface of the lens. At the membrane-water interface, the surfactant molecules are automatically arranged into a hydrophilic outward and lipophilic inward structure on the surface of the lens, so that the surface tension of water is reduced, and water drops spread on the surface of the lens to form a continuous water film, thereby preventing the formation of mist. As the duration of action increases, the surfactant component tends to gradually migrate to the water-air interface due to the continuously formed water film, where the hydrophilic group of the surfactant molecule faces the water layer and the lipophilic group faces the air layer. If the water film is continuously thickened to a certain degree, the water film can be accumulated into drops due to the action of gravity, so that surfactant molecules adsorbed on the surface layer of the water film are directly taken away. If the water film is thin, the water film can naturally surface dry in the air. In both cases, the surfactant molecules migrate to different extents, which results in structural defects in the otherwise closely arranged anti-fog coating, degrading the anti-fog effect and shortening the anti-fog duration. Most anti-fog products on the market suffer from this problem.
The chitosan is a product of removing partial acetyl of natural polysaccharide chitin, contains a large number of primary amino groups in a side chain structure, and can carry out complexation reaction with anionic polyelectrolyte such as alginate in aqueous solution to form a high molecular semipermeable membrane formed by polyelectrolyte complex. However, since chitosan itself has limited water solubility and complex reaction with alginate is liable to cause coagulation reaction, there are few reports on its application in antifog cleaning glasses wet tissues.
Disclosure of Invention
In order to solve the problems, the chitosan is modified to have wide solubility, and the modified chitosan is compounded with alginate and amphoteric surfactant by controlling the amino retention in the chitosan, so that the novel antifogging cleaning glasses wet tissue is provided, and the problem that the antifogging duration is short due to the fact that the migration of surfactant molecules is easy to occur is solved.
Specifically, the invention provides an anti-fog cleaning glasses wet tissue which comprises a substrate and an anti-fog cleaning solution added to the substrate, wherein the anti-fog cleaning solution comprises the following raw materials in percentage by mass: 4-10% of modified chitosan, 10-15% of alginate, 5-8% of amphoteric surfactant, 2-5% of glycerol, 30-40% of absolute ethyl alcohol and the balance of deionized water.
More specifically, the modified chitosan was prepared as follows:
dissolving chitosan and an amino protective agent in a mixed solution of organic amine and chloralkane, stirring and heating under argon atmosphere to react so as to carry out amino protection on the chitosan, slowly dripping an acylating agent, continuously reacting for 3-6 hours, heating to reflux for 6-10 hours, cooling the reaction solution to room temperature, repeatedly carrying out solid-liquid separation, adding an amino protective agent for deprotection, and carrying out vacuum drying to obtain the modified chitosan.
More specifically, the chitosan has a degree of deacetylation of 70 to 90% and a weight average molecular weight of 100000 ~ 800000.
More specifically, the amino protecting agent is methanesulfonic acid, phthalic anhydride, formaldehyde or benzaldehyde.
More specifically, the mass ratio of chitosan to amino protective agent is 1:0.5-1.
More specifically, the heating reaction is to heat to 110-130 ℃ for 4-16 hours.
More specifically, the organic amine is one or more of ethylamine, diethylamine, or triethylamine.
More specifically, the chlorinated alkane is one or more of dichloromethane, chloroform or carbon tetrachloride.
More specifically, the volume ratio of the organic amine to the chloralkane is 1:1-5.
More specifically, the acylating agent is one or more of dodecanoyl chloride, tetradecanoyl chloride, hexadecanoyl chloride, or octadecanoyl chloride.
More specifically, the molar ratio of chitosan to acylating agent is 1:1-9.
More specifically, the amino deprotection agent is ammonia water or hydrazine hydrate.
More specifically, the alginate is sodium alginate.
More specifically, the amphoteric surfactant is a betaine-type surfactant.
More specifically, the betaine type surfactant includes one or more of cocamidopropyl betaine, octyl/decyl amidopropyl betaine, ricinoleic amidopropyl betaine, dodecyl ethoxysulfobetaine, dodecyl hydroxypropyl sulfobetaine, dodecyl sulfobetaine, and lauroyl propyl betaine.
More specifically, the substrate may be a nonwoven fabric, woven cloth, paper, or the like.
More specifically, the substrate is a nonwoven fabric.
The invention also provides a production process of the antifogging cleaning glasses wet towel, which comprises the steps of mixing together modified chitosan, alginate, glycerol, absolute ethanol and deionized water according to the mass ratio, adding an ampholytic surfactant after uniformly stirring, continuously stirring for a period of time to obtain an antifogging cleaning solution, and adding the antifogging cleaning solution into a base material to obtain the antifogging cleaning glasses wet towel.
More specifically, the mass ratio of the anti-fog cleaning solution to the substrate is 1-3:1.
More specifically, the substrate may be a nonwoven fabric, woven cloth, paper, or the like.
More specifically, the substrate is a nonwoven fabric.
More specifically, the means for adding the anti-fog cleaning solution to the substrate includes dipping or spraying.
More specifically, the modified chitosan was prepared as follows:
dissolving chitosan and an amino protective agent in a mixed solution of organic amine and chloralkane, stirring and heating under argon atmosphere to react so as to carry out amino protection on the chitosan, slowly dripping an acylating agent, continuously reacting for 3-6 hours, heating to reflux for 6-10 hours, cooling the reaction solution to room temperature, repeatedly carrying out solid-liquid separation, adding an amino protective agent for deprotection, and carrying out vacuum drying to obtain the modified chitosan.
More specifically, the chitosan has a degree of deacetylation of 70 to 90% and a weight average molecular weight of 100000 ~ 800000.
More specifically, the amino protecting agent is methanesulfonic acid, phthalic anhydride, formaldehyde or benzaldehyde.
More specifically, the mass ratio of chitosan to amino protective agent is 1:0.5-1.
More specifically, the heating reaction is to heat to 110-130 ℃ for 4-16 hours.
More specifically, the organic amine is one or more of ethylamine, diethylamine, or triethylamine.
More specifically, the chlorinated alkane is one or more of dichloromethane, chloroform or carbon tetrachloride.
More specifically, the volume ratio of the organic amine to the chloralkane is 1:1-5.
More specifically, the acylating agent is one or more of dodecanoyl chloride, tetradecanoyl chloride, hexadecanoyl chloride, or octadecanoyl chloride.
More specifically, the molar ratio of chitosan to acylating agent is 1:1-9.
More specifically, the amino deprotection agent is ammonia water or hydrazine hydrate.
More specifically, the alginate is sodium alginate.
More specifically, the amphoteric surfactant is a betaine-type surfactant.
More specifically, the betaine type surfactant includes one or more of cocamidopropyl betaine, octyl/decyl amidopropyl betaine, ricinoleic amidopropyl betaine, dodecyl ethoxysulfobetaine, dodecyl hydroxypropyl sulfobetaine, dodecyl sulfobetaine, and lauroyl propyl betaine.
The beneficial effects of the invention are that
According to the invention, the chitosan is modified to ensure that the chitosan has wide solubility, and the complexing reaction of the modified chitosan and the alginate is controlled by controlling the amino retention in the modification process of the chitosan, so that the modified chitosan does not generate a coagulation reaction, and the modified chitosan is suitable for preparing the antifogging cleaning glasses wet tissues. Meanwhile, the amphoteric surfactant can also be subjected to partial complexation reaction with chitosan and alginate in the process of compounding with chitosan and alginate, so that the amphoteric surfactant can be inserted into a network structure of chitosan and alginate, and therefore, in actual application, the amphoteric surfactant can be retained on a lens for a long time, and the problem that the antifogging duration is short due to the fact that surfactant molecules are easy to migrate on the lens is solved.
Detailed Description
The present invention is further illustrated below with reference to specific examples, which are not intended to limit the invention in any way. Unless specifically stated otherwise, the reagents, methods and apparatus employed in the present invention are those conventional in the art.
Example 1:
preparation of modified chitosan:
chitosan (3.5 g) having a degree of deacetylation of 85% and a weight average molecular weight of 200000 and phthalic anhydride (1.75 g) were added to a mixed solution of 50ml of triethylamine and 90ml of chloroform, stirred under an argon atmosphere and heated to 120 ℃. After 8 hours of reaction, the reaction mixture was cooled to room temperature, and then 25.0g of hexadecanoyl chloride dissolved in 40ml of chloroform was slowly added dropwise to the above-mentioned system, and after 5 hours of reaction, the reaction mixture was slowly warmed to reflux and refluxed for 8 hours. After cooling to room temperature, the reaction solution is subjected to repeated solid-liquid separation, and ammonia water is added to carry out amino deprotection. Finally, vacuum drying to obtain the modified chitosan with wide solubility.
Preparation of anti-fog cleaning solution:
the anti-fog cleaning solution comprises the following raw materials in percentage by mass: 10% of modified chitosan, 15% of sodium alginate, 8% of dodecyl hydroxypropyl sulfobetaine, 5% of glycerol, 40% of absolute ethyl alcohol and the balance of deionized water.
Mixing the modified chitosan, sodium alginate, glycerol, absolute ethyl alcohol and deionized water according to the mass ratio, uniformly stirring, adding dodecyl hydroxypropyl sulfobetaine, and continuously stirring for 30min to obtain the anti-fog cleaning solution.
Preparation of antifogging cleaning glasses wet tissues:
the antifogging cleaning solution is added into non-woven fabrics through dipping according to the mass ratio of 1.5:1, and then the wet tissues are cut according to the actual required size, so that the required wet tissues are prepared.
Example 2:
preparation of modified chitosan:
chitosan (3.5 g) having a degree of deacetylation of 85% and a weight average molecular weight of 200000 and phthalic anhydride (2.5 g) were added to a mixed solution of 50ml of triethylamine and 90ml of chloroform, stirred under an argon atmosphere and heated to 120 ℃. After 8 hours of reaction, the reaction mixture was cooled to room temperature, and then 25.0g of hexadecanoyl chloride dissolved in 40ml of chloroform was slowly added dropwise to the above-mentioned system, and after 5 hours of reaction, the reaction mixture was slowly warmed to reflux and refluxed for 8 hours. After cooling to room temperature, the reaction solution is subjected to repeated solid-liquid separation, and ammonia water is added to carry out amino deprotection. Finally, vacuum drying to obtain the modified chitosan with wide solubility.
Preparation of anti-fog cleaning solution:
the anti-fog cleaning solution comprises the following raw materials in percentage by mass: 8% of modified chitosan, 12% of sodium alginate, 5% of dodecyl hydroxypropyl sulfobetaine, 2% of glycerol, 30% of absolute ethyl alcohol and the balance of deionized water.
Mixing the modified chitosan, sodium alginate, glycerol, absolute ethyl alcohol and deionized water according to the mass ratio, uniformly stirring, adding dodecyl hydroxypropyl sulfobetaine, and continuously stirring for 30min to obtain the anti-fog cleaning solution.
Preparation of antifogging cleaning glasses wet tissues:
the antifogging cleaning solution is added into non-woven fabrics through dipping according to the mass ratio of 1.5:1, and then the wet tissues are cut according to the actual required size, so that the required wet tissues are prepared.
Example 3:
preparation of modified chitosan:
chitosan (3.5 g) having a degree of deacetylation of 85% and a weight average molecular weight of 200000 and phthalic anhydride (3.5 g) were added to a mixed solution of 50ml of triethylamine and 90ml of chloroform, stirred under an argon atmosphere and heated to 120 ℃. After 8 hours of reaction, the reaction mixture was cooled to room temperature, and then 25.0g of hexadecanoyl chloride dissolved in 40ml of chloroform was slowly added dropwise to the above-mentioned system, and after 5 hours of reaction, the reaction mixture was slowly warmed to reflux and refluxed for 8 hours. After cooling to room temperature, the reaction solution is subjected to repeated solid-liquid separation, and ammonia water is added to carry out amino deprotection. Finally, vacuum drying to obtain the modified chitosan with wide solubility.
Preparation of anti-fog cleaning solution:
the anti-fog cleaning solution comprises the following raw materials in percentage by mass: 4% of modified chitosan, 10% of sodium alginate, 6% of dodecyl hydroxypropyl sulfobetaine, 3% of glycerol, 35% of absolute ethyl alcohol and the balance of deionized water.
Mixing the modified chitosan, sodium alginate, glycerol, absolute ethyl alcohol and deionized water according to the mass ratio, uniformly stirring, adding dodecyl hydroxypropyl sulfobetaine, and continuously stirring for 30min to obtain the anti-fog cleaning solution.
Preparation of antifogging cleaning glasses wet tissues:
the antifogging cleaning solution is added into non-woven fabrics through dipping according to the mass ratio of 1.5:1, and then the wet tissues are cut according to the actual required size, so that the required wet tissues are prepared.
Comparative example 1
This comparative example is substantially the same as example 1 except that modified chitosan is not used.
The results show that chitosan and sodium alginate are not suitable for impregnating a non-woven fabric substrate to prepare wet tissues due to coagulation caused by complexation reaction of chitosan and sodium alginate during preparation of the anti-fog cleaning solution.
Comparative example 2
This comparative example was substantially the same as in example 1 except that the amount of phthalic anhydride added was 1.0g.
Comparative example 3
This comparative example was substantially the same as in example 1 except that the amount of phthalic anhydride added was 1.5g.
Comparative example 4
This comparative example was substantially the same as in example 1 except that the amount of phthalic anhydride added was 4.0g.
Comparative example 5
This comparative example was substantially the same as in example 1 except that the amount of phthalic anhydride added was 4.5g.
Comparative example 6
This comparative example provides an anti-fog cleaning eyeglass wet wipe prepared as follows:
preparation of anti-fog cleaning solution:
the anti-fog cleaning solution comprises the following raw materials in percentage by mass: 6% of dodecyl hydroxypropyl sulfobetaine, 3% of glycerol, 35% of absolute ethyl alcohol and the balance of deionized water.
Mixing dodecyl hydroxypropyl sulfobetaine, glycerol, absolute ethyl alcohol and deionized water together according to the mass ratio, and stirring for 30min to obtain the anti-fog cleaning solution.
Preparation of antifogging cleaning glasses wet tissues:
the antifogging cleaning solution is added into non-woven fabrics through dipping according to the mass ratio of 1.5:1, and then the wet tissues are cut according to the actual required size, so that the required wet tissues are prepared.
Test case
Anti-fog effect test on anti-fog cleaning glasses wet tissues prepared in examples 1 to 3 and comparative examples 2 to 6:
the prepared antifog cleaning glasses wet tissues are uniformly smeared with round lenses, and then are placed above a water bath kettle with the temperature of 70 ℃ and the distance from the water surface to the height of 5cm. Taking down the lens after continuously fumigating for 3min, naturally airing the lens, and continuously fumigating the lens on a water bath kettle at 70 ℃ for 3min, so that the lens is reciprocated until fog appears in 10% of the area of the surface of the lens. The test results are shown in table 1 below:
TABLE 1
Figure BDA0004149188580000081
Figure BDA0004149188580000091
Note that: "-" means not hazed; "+" indicates that there is water vapor or fog on the edge, but not more than 10%; "++" indicates that more than 10% of the area is hazed.
As can be seen from the results of table 1, when chitosan and sodium alginate were not used (comparative example 6), the antifogging duration of the antifogging cleaning spectacle wet tissues was short. When the modified chitosan of the present invention is used in combination with sodium alginate and amphoteric surfactant (examples 1-3), the duration of anti-fog for the anti-fog cleaning eyeglass wet wipe is significantly increased. When the addition amount of the amino-protecting agent is controlled to control the amino-preserving amount during the modification of chitosan, the antifogging duration of the antifogging cleaning eyeglass wet tissues tends to increase and decrease with the increase of the addition amount of the amino-protecting agent. This is probably due to the fact that when the added amount of the amino protecting agent is small, the amino groups on the modified chitosan molecular chain are excessively lost in the modification process, so that the complexation reaction with sodium alginate is insufficient to form a network structure for stabilizing the amphoteric surfactant; when the added amount of the amino protective agent is large, the complex reaction of the modified chitosan and the sodium alginate is strong, so that the amphoteric surfactant is difficult to be inserted into the network structure of the chitosan and the alginate, thereby adversely affecting the stabilizing effect of the amphoteric surfactant.
In the description of the specification, reference to the term "one embodiment," "a particular embodiment," "an example," etc., means that a particular feature, structure, material, or characteristic described in connection with the embodiment or example is included in at least one embodiment or example of the invention. In this specification, schematic representations of the above terms do not necessarily refer to the same embodiments or examples. Furthermore, the particular features, structures, materials, or characteristics described may be combined in any suitable manner in any one or more embodiments or examples.
The foregoing is merely illustrative and explanatory of the invention, as various modifications and additions may be made to the particular embodiments described, or by similar arrangements, by those skilled in the art, without departing from the scope of the invention or beyond the scope of the appended claims.

Claims (10)

1. An anti-fog cleaning glasses wet tissue is characterized by comprising a substrate and an anti-fog cleaning solution added to the substrate, wherein the anti-fog cleaning solution comprises the following raw materials in percentage by mass: 4-10% of modified chitosan, 10-15% of alginate, 5-8% of amphoteric surfactant, 2-5% of glycerol, 30-40% of absolute ethyl alcohol and the balance of deionized water.
2. The anti-fog, cleaning eyeglass wet wipe of claim 1 wherein the modified chitosan is prepared as follows:
dissolving chitosan and an amino protective agent in a mixed solution of organic amine and chloralkane, stirring and heating under argon atmosphere to react so as to carry out amino protection on the chitosan, slowly dripping an acylating agent, continuously reacting for 3-6 hours, heating to reflux for 6-10 hours, cooling the reaction solution to room temperature, repeatedly carrying out solid-liquid separation, adding an amino protective agent for deprotection, and carrying out vacuum drying to obtain the modified chitosan.
3. The antifogging cleaning spectacle wet towel according to claim 2, wherein chitosan has a degree of deacetylation of 70 to 90% and a weight-average molecular weight of 100000 ~ 800000,
the amino protective agent is methane sulfonic acid, phthalic anhydride, formaldehyde or benzaldehyde,
the mass ratio of the chitosan to the amino protective agent is 1:0.5-1,
the amino deprotection agent is ammonia water or hydrazine hydrate.
4. The anti-fog cleaning eyeglass wet tissue according to claim 2, wherein the organic amine is one or more of ethylamine, diethylamine or triethylamine,
the chlorinated alkane is one or more of dichloromethane, chloroform or carbon tetrachloride, the volume ratio of the organic amine to the chlorinated alkane is 1:1-5,
the acylating agent is one or more of dodecanoyl chloride, tetradecanoyl chloride, hexadecanoyl chloride or octadecanoyl chloride,
the molar ratio of chitosan to acylating agent is 1:1-9.
5. The anti-fog cleaning eyeglass wet tissue according to claim 1, wherein the alginate is sodium alginate,
the amphoteric surfactant is betaine surfactant.
6. The anti-fog, cleaning eyeglass wet wipe of claim 1 wherein the substrate is a nonwoven.
7. The process for producing an antifogging cleaning spectacle wet towel according to any one of claims 1 to 6, comprising
Mixing modified chitosan, alginate, glycerol, absolute ethyl alcohol and deionized water together according to the mass ratio, adding an ampholytic surfactant after uniformly stirring, continuously stirring for a period of time to obtain an anti-fog cleaning solution,
and adding the anti-fog cleaning solution into a substrate to obtain the anti-fog cleaning glasses wet tissue.
8. The production process according to claim 7, wherein the mass ratio of the anti-fog cleaning solution to the substrate is 1-3:1.
9. The process of claim 7, wherein the substrate is a nonwoven fabric.
10. The process of claim 7, wherein the means for adding the anti-fog cleaning solution to the substrate comprises dipping or spraying.
CN202310312971.9A 2023-03-28 2023-03-28 Antifogging cleaning glasses wet tissue and production process thereof Pending CN116333832A (en)

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Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN116904077A (en) * 2023-09-13 2023-10-20 山东森博斯特塑胶科技有限公司 PO film coating liquid and preparation method thereof

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN116904077A (en) * 2023-09-13 2023-10-20 山东森博斯特塑胶科技有限公司 PO film coating liquid and preparation method thereof
CN116904077B (en) * 2023-09-13 2023-11-24 山东森博斯特塑胶科技有限公司 PO film coating liquid and preparation method thereof

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