CN113214548A - Natural foaming material - Google Patents
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- CN113214548A CN113214548A CN202110543136.7A CN202110543136A CN113214548A CN 113214548 A CN113214548 A CN 113214548A CN 202110543136 A CN202110543136 A CN 202110543136A CN 113214548 A CN113214548 A CN 113214548A
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- 238000005187 foaming Methods 0.000 title claims abstract description 50
- 239000000463 material Substances 0.000 title claims abstract description 29
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 claims abstract description 45
- 239000011259 mixed solution Substances 0.000 claims abstract description 33
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 claims abstract description 30
- 230000002936 tranquilizing effect Effects 0.000 claims abstract description 23
- VYFYYTLLBUKUHU-UHFFFAOYSA-N dopamine Chemical compound NCCC1=CC=C(O)C(O)=C1 VYFYYTLLBUKUHU-UHFFFAOYSA-N 0.000 claims abstract description 22
- 229940125725 tranquilizer Drugs 0.000 claims abstract description 22
- 239000003204 tranquilizing agent Substances 0.000 claims abstract description 22
- RRHGJUQNOFWUDK-UHFFFAOYSA-N Isoprene Chemical compound CC(=C)C=C RRHGJUQNOFWUDK-UHFFFAOYSA-N 0.000 claims abstract description 17
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 claims abstract description 15
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims abstract description 15
- 229940049964 oleate Drugs 0.000 claims abstract description 15
- ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(O)=O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 claims abstract description 15
- 239000011591 potassium Substances 0.000 claims abstract description 15
- 229910052700 potassium Inorganic materials 0.000 claims abstract description 15
- VAKMIIPDYZXBEV-DPMBMXLASA-M potassium;(z,12r)-12-hydroxyoctadec-9-enoate Chemical compound [K+].CCCCCC[C@@H](O)C\C=C/CCCCCCCC([O-])=O VAKMIIPDYZXBEV-DPMBMXLASA-M 0.000 claims abstract description 15
- 239000011593 sulfur Substances 0.000 claims abstract description 15
- 229910052717 sulfur Inorganic materials 0.000 claims abstract description 15
- 235000013311 vegetables Nutrition 0.000 claims abstract description 15
- 238000004073 vulcanization Methods 0.000 claims abstract description 15
- 239000011787 zinc oxide Substances 0.000 claims abstract description 15
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 claims abstract description 13
- 239000011734 sodium Substances 0.000 claims abstract description 13
- 229910052708 sodium Inorganic materials 0.000 claims abstract description 13
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 13
- 239000006185 dispersion Substances 0.000 claims abstract description 11
- 229960003638 dopamine Drugs 0.000 claims abstract description 11
- 238000002360 preparation method Methods 0.000 claims abstract description 4
- 239000003795 chemical substances by application Substances 0.000 claims description 15
- 238000009210 therapy by ultrasound Methods 0.000 claims description 9
- -1 sodium fluorosilicate Chemical compound 0.000 claims 2
- 239000006261 foam material Substances 0.000 claims 1
- 238000000034 method Methods 0.000 claims 1
- 230000001914 calming effect Effects 0.000 abstract description 5
- 210000005036 nerve Anatomy 0.000 abstract description 5
- 229920000858 Cyclodextrin Polymers 0.000 abstract description 2
- 230000009982 effect on human Effects 0.000 abstract description 2
- 239000000126 substance Substances 0.000 abstract description 2
- 239000000203 mixture Substances 0.000 description 14
- 230000003860 sleep quality Effects 0.000 description 11
- 230000003247 decreasing effect Effects 0.000 description 6
- 208000013738 Sleep Initiation and Maintenance disease Diseases 0.000 description 3
- 206010022437 insomnia Diseases 0.000 description 3
- 239000003814 drug Substances 0.000 description 2
- 229940079593 drug Drugs 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 230000004048 modification Effects 0.000 description 2
- 238000012986 modification Methods 0.000 description 2
- 208000007443 Neurasthenia Diseases 0.000 description 1
- 206010003549 asthenia Diseases 0.000 description 1
- 210000004556 brain Anatomy 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 201000010099 disease Diseases 0.000 description 1
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 230000007774 longterm Effects 0.000 description 1
- 230000003340 mental effect Effects 0.000 description 1
- 239000002861 polymer material Substances 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
Classifications
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J9/00—Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof
- C08J9/0095—Mixtures of at least two compounding ingredients belonging to different one-dot groups
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J9/00—Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof
- C08J9/0014—Use of organic additives
- C08J9/0023—Use of organic additives containing oxygen
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J9/00—Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof
- C08J9/0061—Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof characterized by the use of several polymeric components
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J9/00—Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof
- C08J9/0066—Use of inorganic compounding ingredients
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J9/00—Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof
- C08J9/009—Use of pretreated compounding ingredients
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J2307/00—Characterised by the use of natural rubber
- C08J2307/02—Latex
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J2405/00—Characterised by the use of polysaccharides or of their derivatives not provided for in groups C08J2401/00 or C08J2403/00
- C08J2405/16—Cyclodextrin; Derivatives thereof
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K13/00—Use of mixtures of ingredients not covered by one single of the preceding main groups, each of these compounds being essential
- C08K13/06—Pretreated ingredients and ingredients covered by the main groups C08K3/00 - C08K7/00
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K3/00—Use of inorganic substances as compounding ingredients
- C08K3/18—Oxygen-containing compounds, e.g. metal carbonyls
- C08K3/20—Oxides; Hydroxides
- C08K3/22—Oxides; Hydroxides of metals
- C08K2003/2296—Oxides; Hydroxides of metals of zinc
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K3/00—Use of inorganic substances as compounding ingredients
- C08K3/02—Elements
- C08K3/06—Sulfur
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K3/00—Use of inorganic substances as compounding ingredients
- C08K3/34—Silicon-containing compounds
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/04—Oxygen-containing compounds
- C08K5/05—Alcohols; Metal alcoholates
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/04—Oxygen-containing compounds
- C08K5/09—Carboxylic acids; Metal salts thereof; Anhydrides thereof
- C08K5/098—Metal salts of carboxylic acids
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/04—Oxygen-containing compounds
- C08K5/10—Esters; Ether-esters
- C08K5/101—Esters; Ether-esters of monocarboxylic acids
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/04—Oxygen-containing compounds
- C08K5/15—Heterocyclic compounds having oxygen in the ring
- C08K5/151—Heterocyclic compounds having oxygen in the ring having one oxygen atom in the ring
- C08K5/1545—Six-membered rings
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K9/00—Use of pretreated ingredients
- C08K9/04—Ingredients treated with organic substances
Abstract
The invention provides a preparation method of a natural foaming material, which comprises the following steps: grinding the tranquilizer and dopamine in a grinding machine, adding into natural latex, sulfur, vulcanization accelerator, zinc oxide, potassium ricinoleate, potassium vegetable oleate, potassium hydroxide and 2-hydroxy cyclodextrin, uniformly mixing by using a high-speed dispersion machine to form a mixed solution, curing for 8-12h in a water bath at the constant temperature of 28 ℃, mixing with sodium fluosilicate, foaming by using a high-speed foaming machine, and vulcanizing to obtain the foaming material. The natural foaming material provided by the invention adopts natural components, is not added with other harmful chemical components, has no harm or side effect on human bodies, and simultaneously has the functions of soothing the nerves and calming the heart, thereby improving the sleeping quality of people.
Description
Technical Field
The invention relates to the field of high polymer materials, in particular to a natural foaming material, and specifically relates to a natural foaming material with nerve calming and heart calming effects.
Background
People who have insomnia in the modern times are more and more, the insomnia is mainly caused by insufficient exercise amount, heavy mental stress or excessive pressure to interfere sleep, severe activities are carried out before sleep, the brain is still in a highly tense state when the people fall asleep, the insomnia is caused, and diseases such as neurasthenia and the like can be induced by low-quality sleep, so that normal life is influenced. Some people can sleep with the help of sleep-improving medicines, but the medicines have great harm to the nerves of people, and can generate dependence after long-term use, thereby affecting the health of people.
Disclosure of Invention
Aiming at the technical problems in the prior art, the molecular structure with the nerve-soothing effect is added into the natural latex, the natural latex is uniformly mixed, and the novel natural foaming material with the functions of calming the heart, soothing the nerves and improving the sleep quality of people is prepared through foaming and vulcanizing. The natural foaming material is characterized by comprising a modified nerve-soothing agent, wherein the nerve-soothing agent is one or more of a nerve-soothing agent A, a nerve-soothing agent B and a nerve-soothing agent C, and the nerve-soothing agent A is:
the tranquilizer B is
The tranquilizer C is
Preferably, the preparation method of the modified tranquilizer comprises the following steps: dispersing the tranquilizer and dopamine in water, grinding at room temperature for 10min, and performing ultrasonic treatment for 30-60min to obtain modified tranquilizer. More preferably, the weight part ratio of the tranquilizer to the dopamine is 1: 1.
Preferably, the natural foaming material also comprises natural latex, sulfur, a vulcanization accelerator, zinc oxide, potassium ricinoleate, potassium vegetable oleate, potassium hydroxide, 2-hydroxycyclodextrin and sodium fluosilicate.
Preferably, the natural foaming material comprises, by weight, 167 parts of natural latex, 2 parts of sulfur, 2 parts of a vulcanization accelerator, 2 parts of zinc oxide, 4 parts of potassium ricinoleate, 4 parts of potassium vegetable oleate, 1 part of potassium hydroxide, 1 part of 2-hydroxycyclodextrin, 3 parts of sodium fluosilicate and 0.1-5 parts of a modifying tranquilizer.
A preparation method of a natural foaming material comprises the following steps:
adding the modified nerve-soothing agent into natural latex, sulfur, a vulcanization accelerator, zinc oxide, potassium ricinoleate, potassium vegetable oleate, potassium hydroxide and 2-hydroxycyclodextrin, uniformly mixing by using a high-speed dispersion machine to form a mixed solution, curing for 8-12h under the condition of water bath constant temperature of 28 ℃, mixing with sodium fluosilicate, foaming by using a high-speed foaming machine, and vulcanizing to obtain the foaming material.
It is a further object of the present invention to provide the use of the above natural foamed material, which can be applied in the field of bedding.
The natural foaming material provided by the invention adopts the natural components, does not contain other harmful chemical components, has no harm or side effect on human bodies, can play the roles of soothing the nerves and calming the heart at the same time, and improves the sleeping quality of people.
Detailed Description
The invention will be further described with reference to specific examples:
the evaluation of the tranquilizing effect adopts Pittsburgh sleep quality index, and the lower the index, the better the sleep quality. The present data are from statistics of 100 samples. The parts in the following examples are parts by weight.
Example 1
Grinding 0.1 part of tranquilizer A and 0.1 part of dopamine at normal temperature for 10min, then carrying out ultrasonic treatment for 30-60min, adding the mixture into 167 parts of natural latex, 2 parts of sulfur, 2 parts of vulcanization accelerator, 2 parts of zinc oxide, 4 parts of potassium ricinoleate, 4 parts of potassium vegetable oleate, 1 part of potassium hydroxide and 1 part of 2-hydroxycyclodextrin, uniformly mixing the mixture by using a high-speed dispersion machine to form a mixed solution, curing the mixed solution for 8-12h in water bath at the constant temperature of 28 ℃, mixing 3 parts of sodium fluosilicate, foaming the mixed solution by using a high-speed foaming machine, and vulcanizing the mixed solution to obtain the foaming material. The pittsburgh sleep quality index is reduced by 10%.
Example 2
Grinding 5 parts of tranquilizer A and 0.5 part of dopamine at normal temperature for 10min, then carrying out ultrasonic treatment for 30-60min, adding the mixture into 167 parts of natural latex, 2 parts of sulfur, 2 parts of vulcanization accelerator, 2 parts of zinc oxide, 4 parts of potassium ricinoleate, 4 parts of potassium vegetable oleate, 1 part of potassium hydroxide and 1 part of 2-hydroxycyclodextrin, uniformly mixing the mixture by using a high-speed dispersion machine to form a mixed solution, curing the mixed solution for 8-12h in water bath at the constant temperature of 28 ℃, mixing 3 parts of sodium fluosilicate, foaming the mixed solution by using a high-speed foaming machine, and vulcanizing the mixed solution to obtain the foaming material. The pittsburgh sleep quality index decreased by 21%.
Example 3
Grinding 0.1 part of tranquilizer B and 0.1 part of dopamine at normal temperature for 10min, then carrying out ultrasonic treatment for 30-60min, adding the mixture into 167 parts of natural latex, 2 parts of sulfur, 2 parts of vulcanization accelerator, 2 parts of zinc oxide, 4 parts of potassium ricinoleate, 4 parts of potassium vegetable oleate, 1 part of potassium hydroxide and 1 part of 2-hydroxycyclodextrin, uniformly mixing the mixture by using a high-speed dispersion machine to form a mixed solution, curing the mixed solution for 8-12h in water bath at the constant temperature of 28 ℃, mixing 3 parts of sodium fluosilicate, foaming the mixed solution by using a high-speed foaming machine, and vulcanizing the mixed solution to obtain the foaming material. The pittsburgh sleep quality index decreased by 12%.
Example 4
Grinding 5 parts of tranquilizer B and 0.5 part of dopamine at normal temperature for 10min, then carrying out ultrasonic treatment for 30-60min, adding the mixture into 167 parts of natural latex, 2 parts of sulfur, 2 parts of vulcanization accelerator, 2 parts of zinc oxide, 4 parts of potassium ricinoleate, 4 parts of potassium vegetable oleate, 1 part of potassium hydroxide and 1 part of 2-hydroxycyclodextrin, uniformly mixing the mixture by using a high-speed dispersion machine to form a mixed solution, curing the mixed solution for 8-12h in water bath at the constant temperature of 28 ℃, mixing 3 parts of sodium fluosilicate, foaming the mixed solution by using a high-speed foaming machine, and vulcanizing the mixed solution to obtain the foaming material. Pittsburgh sleep quality index decreased by 19%.
Example 5
Grinding 0.1 part of tranquilizer C and 0.1 part of dopamine at normal temperature for 10min, then carrying out ultrasonic treatment for 30-60min, adding the mixture into 167 parts of natural latex, 2 parts of sulfur, 2 parts of vulcanization accelerator, 2 parts of zinc oxide, 4 parts of potassium ricinoleate, 4 parts of potassium vegetable oleate, 1 part of potassium hydroxide and 1 part of 2-hydroxycyclodextrin, uniformly mixing the mixture by using a high-speed dispersion machine to form a mixed solution, curing the mixed solution for 8-12h in water bath at the constant temperature of 28 ℃, mixing 3 parts of sodium fluosilicate, foaming the mixed solution by using a high-speed foaming machine, and vulcanizing the mixed solution to obtain the foaming material. The pittsburgh sleep quality index decreased by 9%.
Example 6
Grinding 0.5 part of tranquilizer C and 0.5 part of dopamine at normal temperature for 10min, then carrying out ultrasonic treatment for 30-60min, adding the mixture into 167 parts of natural latex, 2 parts of sulfur, 2 parts of vulcanization accelerator, 2 parts of zinc oxide, 4 parts of potassium ricinoleate, 4 parts of potassium vegetable oleate, 1 part of potassium hydroxide and 1 part of 2-hydroxycyclodextrin, uniformly mixing the mixture by using a high-speed dispersion machine to form a mixed solution, curing the mixed solution for 8-12h in water bath at the constant temperature of 28 ℃, mixing 3 parts of sodium fluosilicate, foaming the mixed solution by using a high-speed foaming machine, and vulcanizing the mixed solution to obtain the foaming material. The pittsburgh sleep quality index decreased by 18%.
Example 7
Grinding 1 part of tranquilizer, 2 parts of tranquilizer B, 3.5 parts of tranquilizer C and 6.5 parts of dopamine at normal temperature for 10min, then carrying out ultrasonic treatment for 30-60min, adding the mixture into 167 parts of natural latex, 2 parts of sulfur, 2 parts of vulcanization accelerator, 2 parts of zinc oxide, 4 parts of potassium ricinoleate, 4 parts of potassium vegetable oleate, 1 part of potassium hydroxide and 1 part of 2-hydroxycyclodextrin, uniformly mixing the mixture by using a high-speed dispersion machine to form a mixed solution, curing the mixed solution for 8-12h in a water bath at the constant temperature of 28 ℃, mixing 3 parts of sodium fluosilicate, foaming the mixed solution by using a high-speed foaming machine, and vulcanizing the mixed solution to prepare the foaming material. The pittsburgh sleep quality index decreased by 31%.
Comparative example 1
167 parts of natural latex, 2 parts of sulfur, 2 parts of vulcanization accelerator, 2 parts of zinc oxide, 4 parts of potassium ricinoleate, 4 parts of potassium vegetable oleate, 1 part of potassium hydroxide and 1 part of 2-hydroxy cyclodextrin are uniformly mixed by a high-speed dispersion machine to form a mixed solution, after the mixed solution is aged for 8 to 12 hours under the water bath constant temperature condition of 28 ℃, 3 parts of sodium fluosilicate is mixed to be foamed by a high-speed foaming machine and vulcanized, and the foaming material is prepared. The pittsburgh sleep quality index has no obvious change.
The foregoing is directed to preferred embodiments of the present invention, other and further embodiments of the invention may be devised without departing from the basic scope thereof, and the scope thereof is determined by the claims that follow. However, any simple modification, equivalent change and modification of the above embodiments according to the technical essence of the present invention are within the protection scope of the technical solution of the present invention.
Claims (6)
1. The natural foaming material is characterized by comprising a modified nerve-soothing agent, wherein the nerve-soothing agent is one or more of a nerve-soothing agent A, a nerve-soothing agent B and a nerve-soothing agent C, and the nerve-soothing agent A is:
the tranquilizer B is
The tranquilizer C is
2. The natural foaming material of claim 1, wherein the preparation method of the modified nerve-soothing agent comprises the following steps: dispersing the tranquilizer and dopamine in water, grinding at room temperature for 10min, and performing ultrasonic treatment for 30-60min to obtain modified tranquilizer.
3. The natural foam material of claim 1, further comprising natural latex, sulfur, a vulcanization accelerator, zinc oxide, potassium ricinoleate, potassium vegetable oleate, potassium hydroxide, 2-hydroxycyclodextrin, and sodium fluorosilicate.
4. The natural foaming material of claim 3, comprising 167 parts of natural latex, 2 parts of sulfur, 2 parts of vulcanization accelerator, 2 parts of zinc oxide, 4 parts of potassium ricinoleate, 4 parts of potassium vegetable oleate, 1 part of potassium hydroxide, 1 part of 2-hydroxycyclodextrin, 3 parts of sodium fluorosilicate, and 0.1-5 parts of modifying tranquilizer.
5. A method for preparing the natural foaming material of any one of claims 1 to 4, which comprises the following steps: adding the modified nerve-soothing agent into natural latex, sulfur, a vulcanization accelerator, zinc oxide, potassium ricinoleate, potassium vegetable oleate, potassium hydroxide and 2-hydroxycyclodextrin, uniformly mixing by using a high-speed dispersion machine to form a mixed solution, curing for 8-12h under the condition of water bath constant temperature of 28 ℃, mixing with sodium fluosilicate, foaming by using a high-speed foaming machine, and vulcanizing to obtain the foaming material.
6. Use of the natural foaming material of any one of claims 1 to 4 in the bedding field.
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