CN106519320A - Method for preparing high-performance medical special rubber - Google Patents

Method for preparing high-performance medical special rubber Download PDF

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CN106519320A
CN106519320A CN201610935754.5A CN201610935754A CN106519320A CN 106519320 A CN106519320 A CN 106519320A CN 201610935754 A CN201610935754 A CN 201610935754A CN 106519320 A CN106519320 A CN 106519320A
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rubber
parts
preparation
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CN106519320B (en
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李谨宏
陈春明
蒋立地
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Kunming Yunken Rubber Co Ltd
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    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L7/00Compositions of natural rubber
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    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08JWORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
    • C08J3/00Processes of treating or compounding macromolecular substances
    • C08J3/28Treatment by wave energy or particle radiation
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    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L83/00Compositions of macromolecular compounds obtained by reactions forming in the main chain of the macromolecule a linkage containing silicon with or without sulfur, nitrogen, oxygen or carbon only; Compositions of derivatives of such polymers
    • C08L83/04Polysiloxanes
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L9/00Compositions of homopolymers or copolymers of conjugated diene hydrocarbons
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L9/00Compositions of homopolymers or copolymers of conjugated diene hydrocarbons
    • C08L9/02Copolymers with acrylonitrile
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L9/00Compositions of homopolymers or copolymers of conjugated diene hydrocarbons
    • C08L9/06Copolymers with styrene
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08JWORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
    • C08J2307/00Characterised by the use of natural rubber
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08JWORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
    • C08J2309/00Characterised by the use of homopolymers or copolymers of conjugated diene hydrocarbons
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08JWORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
    • C08J2309/00Characterised by the use of homopolymers or copolymers of conjugated diene hydrocarbons
    • C08J2309/02Copolymers with acrylonitrile
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08JWORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
    • C08J2309/00Characterised by the use of homopolymers or copolymers of conjugated diene hydrocarbons
    • C08J2309/06Copolymers with styrene
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08JWORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
    • C08J2383/00Characterised by the use of macromolecular compounds obtained by reactions forming in the main chain of the macromolecule a linkage containing silicon with or without sulfur, nitrogen, oxygen, or carbon only; Derivatives of such polymers
    • C08J2383/04Polysiloxanes
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08KUse of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K2201/00Specific properties of additives
    • C08K2201/011Nanostructured additives
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    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L2201/00Properties
    • C08L2201/08Stabilised against heat, light or radiation or oxydation
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L2205/00Polymer mixtures characterised by other features
    • C08L2205/03Polymer mixtures characterised by other features containing three or more polymers in a blend
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L2205/00Polymer mixtures characterised by other features
    • C08L2205/03Polymer mixtures characterised by other features containing three or more polymers in a blend
    • C08L2205/035Polymer mixtures characterised by other features containing three or more polymers in a blend containing four or more polymers in a blend

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  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Organic Chemistry (AREA)
  • Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
  • Medicinal Preparation (AREA)
  • Compositions Of Macromolecular Compounds (AREA)

Abstract

The invention relates to the field of pharmaceutical rubber, and discloses a method for preparing high-performance medical special rubber. A rubber material is placed in an ultraviolet irradiation reactor for surface activation, the activated rubber is pulverized and added to a surfactant solution to be heated and stirred to react, benzalkonium chloride, tributyltin fluoride, potassium pyrrolidone carboxylate and an antioxidant are added to be heated and stirred to react, and are filtered and dried to obtain a mixture, the mixture is added with graphene and a nano-inorganic fiber to be ultrasonically mixed, and then a plant source extract and lavender essential oil are added to be continuously subjected to ultrasonic reaction, and cooled to obtain the high-performance medical special rubber. The rubber material prepared by the invention has good bending strength and tensile strength, strong corrosion resistance and oxidation resistance, prolonged service life and strong antibacterial function, and infection prevention. The preparation method provided by the invention is simple and feasible, and is suitable for popularization and application in wide range.

Description

A kind of preparation method of high-performance medicine specific rubber
Technical field
The present invention relates to medical rubber materials, and in particular to a kind of preparation method of high-performance medicine specific rubber.
Background technology
Rubber industry is one of important foundation industry of national economy.It is indispensable that it not only provides daily life for people The light industry rubber product such as daily, medical, and carry to the heavy industry such as digging, traffic, building, machinery, electronics and new industry For various rubber system production equipments or rubber components.Medical grade rubber has a wide range of applications in terms of medical material, such as medical silicon Rubber catheter, rubber hose for medical, Medical rubber plug, medical air cushion etc..Pharmaceutical rubber requires nontoxic to body, it is impossible to contain Insalubrious material, hinder health, especially aromatics chemical productss may endanger reproductive function, sensitization, Cause asthma, even cancer.
At present, the mechanical property of existing medical grade rubber needs further to be improved, and corrosion resistance is poor, causes its life-span Substantially reduce, additionally, existing medical grade rubber product antibacterial effect is not ideal enough.Therefore, with medical requirement more and more higher, For the quality requirements also more and more higher of medical grade rubber, thus be accomplished by developing one kind can high performance elastomeric material come more preferable The application requirement for meeting medical field.
The content of the invention
In order to overcome drawbacks described above, the technical problem to be solved in the present invention to be to provide a kind of high-performance medicine specific rubber Preparation method, the rubber have excellent mechanical performance, corrosion resistance, non-oxidizability, and sterilizing ability is strong.
In order to solve above-mentioned technical problem, the technical scheme is that:
A kind of preparation method of high-performance medicine specific rubber, comprises the steps:
(1)The elastomeric material of clean surface is placed in ultraviolet irradiation reactor, irradiation wavelengths 100-350nm, during irradiation Between 30-60s, obtain the rubber of surface active;
(2)The surfactant solution of 2wt%-5wt% is prepared, by step(1)Surface is added to after the rubber pulverizing for obtaining Activator solution, is heated to 60-80 DEG C of stirring reaction 10-20min, adds benzalkonium chloride, fluorination tributyl tin, ketopyrrolidine Carboxylic acid potassium and antioxidant, are heated to 80-120 DEG C, stirring reaction 5-15min, and deionized water filtration drying obtains compound;
(3)By step(2)In the compound input ultrasonic reactor for obtaining, Graphene, the mixing of nano inorganic fiber are added Ultrasonic 2-5min, adds Extracts from Plant Recourses, Herba Lysimachiae foenum-graeci quintessence oil, continues ultrasound 5-15min, and natural cooling obtains high-performance medicine Specific rubber.
Preferably, the rubber be medical natural rubber, silicone rubber, isoprene rubber, nitrile rubber, in butadiene-styrene rubber one Plant or various mixture.
Preferably, the surface modifier is polyvinylpyrrolidone, shitosan, sodium alginate, methoxypolyethylene glycol third One or more mixture in olefin(e) acid ester.
Preferably, the Graphene is the graphene oxide that obtains after concentrated sulphuric acid acidification.
Preferably, the nano inorganic fiber is medical grade gypsum fiber, wollastonite fibre, sepiolite fibre, shepardite One or more mixture in fiber.
Preferably, the Extracts from Plant Recourses for natural plants are size-reduced, the blending that adds water, standing, multiple filtration, vacuum it is dense Contracting, spray drying are obtained.
Preferably, the natural plants are Aloe, Herba Menthae, Bulbus Allii, Radix Sophorae Flavescentiss, one or more mixture in Radix et Caulis Opuntiae Dillenii.
Preferably, the step(2)In each parts by weight of raw materials composition:Rubber 50-80 parts, surfactant 10-20 parts, benzene Prick oronain 10-15 parts, fluorination tributyl tin 8-12 parts, 2-pyrrolidone-5-carboxylic acid's potassium 6-10 parts, antioxidant 5-10 parts.
Preferably, the step(3)In each parts by weight of raw materials composition:Graphene 3-8 parts, nano inorganic fiber 2-10 parts, Extracts from Plant Recourses 1-3 parts, Herba Lysimachiae foenum-graeci quintessence oil 0.5-2 parts.
Preferably, the step(3)Middle supersonic frequency is 200-300MHz.
Compared with prior art the invention has the beneficial effects as follows:
(1)Method for preparing rubber of the present invention, carries out activation processing from ultraviolet radioactive to medical grade rubber, admixed graphite alkene and Nano inorganic fiber, lifts the bending strength and tensile strength of rubber, with good flexibility.
(2)Method for preparing rubber of the present invention, is modified process to the rubber of activation processing from surfactant, with which His component synergism, effectively improves the heat-resisting oxidation-resistance performance and corrosion resistance of rubber, can effectively improve which and use the longevity Life, using the standby medical grade rubber product of rubber system of the present invention without potentially danger, further increase rubber safety and Quality assurance.
(3)Contain natural plant extract in rubber of the present invention, the effect with bacteriostasis and sterilization sterilization can prevent sense Dye, has important function in clinical treatment.
(4)The present invention prepare rubber it is raw materials used easily separate out without sulfur, accelerator etc. or easily pyrolytic into Point, to medicine and tissue without potential toxicity, further increase safety and the quality assurance of rubber.
(5)Preparation method of the present invention is simple, is suitable to popularization and application on a large scale.
Specific embodiment
Below the specific embodiment of the present invention is described further.Here is it should be noted that for these enforcements The explanation of mode is used to help understand the present invention, but does not constitute limitation of the invention.Additionally, invention described below As long as involved technical characteristic does not constitute conflict each other and can just be mutually combined in each embodiment.
Embodiment 1
A kind of preparation method of high-performance medicine specific rubber, comprises the steps:
(1)50 weight portion medical natural rubber materials of clean surface are placed in ultraviolet irradiation reactor, irradiation wavelengths 100nm, exposure time 60s obtain the rubber of surface active;
(2)The polyvinylpyrrolidonesolution solution of 2wt% is prepared, by step(1)Polyethylene is added to after the rubber pulverizing for obtaining Pyrrolidone solution, is heated to 60 DEG C of stirring reactions 20min, adds 10 weight portion benzalkonium chlorides, 8 weight portions fluorination tributyl Stannum, 6 weight portion 2-pyrrolidone-5-carboxylic acid potassium and 5 weight portion antioxidant, are heated to 80 DEG C, stirring reaction 15min, deionized water mistake It is filtered dry dry, obtains compound;
(3)By step(2)In the compound input ultrasonic reactor for obtaining, 3 parts by weight of graphite alkene, 2 weight portions doctor are added Mix ultrasound 2min with level nanometer gypsum fiber, supersonic frequency is 300MHz;Add 1 weight portion Aloe extract, 0.5 weight Part Herba Lysimachiae foenum-graeci quintessence oil, continues ultrasound 15min, and natural cooling obtains high-performance medicine specific rubber.
Embodiment 2
A kind of preparation method of high-performance medicine specific rubber, comprises the steps:
(1)60 weight portion medical grade silicon rubber materials of clean surface are placed in ultraviolet irradiation reactor, irradiation wavelengths 150nm, exposure time 50s obtain the rubber of surface active;
(2)The chitosan solution of 3wt% is prepared, by step(1)Chitosan solution is added to after the rubber pulverizing for obtaining, plus Heat adds 12 weight portion benzalkonium chlorides, 10 weight portions fluorination tributyl tin, 8 weight portion pyrroles to 70 DEG C of stirring reactions 15min Alkanone carboxylic acid potassium and 6 weight portion antioxidant, are heated to 90 DEG C, and stirring reaction 12min, deionized water filtration drying are mixed Close material;
(3)By step(2)In the compound input ultrasonic reactor for obtaining, 5 parts by weight of graphite alkene, 4 weight portions doctor are added Mix ultrasound 3min with level nanometer wollastonite fibre, supersonic frequency is 300MHz;Add 2 weight portion Folium Menthae extracts, 1 weight Part Herba Lysimachiae foenum-graeci quintessence oil, continues ultrasound 12min, and natural cooling obtains high-performance medicine specific rubber.
Embodiment 3
A kind of preparation method of high-performance medicine specific rubber, comprises the steps:
(1)70 weight portions of clean surface medical isoprene rubber material is placed in ultraviolet irradiation reactor, irradiation wavelengths 200nm, exposure time 40s obtain the rubber of surface active;
(2)The sodium alginate soln of 4wt% is prepared, by step(1)Sodium alginate is added to after the rubber pulverizing for obtaining molten Liquid, is heated to 80 DEG C of stirring reactions 10min, adds 15 weight portion benzalkonium chlorides, 12 weight portions fluorination tributyl tin, 10 weight Part 2-pyrrolidone-5-carboxylic acid's potassium and 8 weight portion antioxidant, are heated to 100 DEG C, stirring reaction 10min, deionized water filtration drying, Obtain compound;
(3)By step(2)In the compound input ultrasonic reactor for obtaining, 6 parts by weight of graphite alkene, 6 weight portions doctor are added Mix ultrasound 5min with level nanometer sepiolite fibre, supersonic frequency is 200MHz;Add 3 weight portion Bulbus Allii extracts, 1.5 weights Amount part Herba Lysimachiae foenum-graeci quintessence oil, continues ultrasound 5min, and natural cooling obtains high-performance medicine specific rubber.
Embodiment 4
A kind of preparation method of high-performance medicine specific rubber, comprises the steps:
(1)The medical nitrile rubber of 80 weight portions of clean surface is placed in ultraviolet irradiation reactor, irradiation wavelengths 350nm, exposure time 30s obtain the rubber of surface active;
(2)The methoxypolyethylene glycol acrylate solution of 5wt% is prepared, by step(1)It is added to after the rubber pulverizing for obtaining Methoxypolyethylene glycol acrylate solution, is heated to 70 DEG C of stirring reactions 15min, adds 12 weight portion benzalkonium chlorides, 10 weights Amount part fluorination tributyl tin, 8 weight portion 2-pyrrolidone-5-carboxylic acid potassium and 10 weight portion antioxidant, are heated to 120 DEG C, stirring reaction 5min, deionized water filtration drying, obtains compound;
(3)By step(2)In the compound input ultrasonic reactor for obtaining, 8 parts by weight of graphite alkene, 10 weight portions doctor are added Mix ultrasound 5min with level nanometer brucite fiber, supersonic frequency is 200MHz;Add 3 weight portion Radix Sophorae Flavescentis extracts, 1 weight Part Herba Lysimachiae foenum-graeci quintessence oil, continues ultrasound 8min, and natural cooling obtains high-performance medicine specific rubber.
Embodiment 5
A kind of preparation method of high-performance medicine specific rubber, comprises the steps:
(1)The medical styrene-butadiene rubber of 80 weight portions of clean surface is placed in ultraviolet irradiation reactor, irradiation wavelengths 250nm, exposure time 40s obtain the rubber of surface active;
(2)Polyvinylpyrrolidone, the shitosan mixed solution of 3wt% are prepared, by step(1)After the rubber pulverizing for obtaining Mixed solution is added to, 60 DEG C of stirring reactions 20min are heated to, 10 weight portion benzalkonium chlorides, 12 weight portions fluorination three is added Butyl tin, 8 weight portion 2-pyrrolidone-5-carboxylic acid potassium and 6 weight portion antioxidant, are heated to 100 DEG C, stirring reaction 12min, spend from Sub- water filtration is dried, and obtains compound;
(3)By step(2)In the compound input ultrasonic reactor for obtaining, 6 parts by weight of graphite alkene, 4 weight portions doctor are added With level nanometer gypsum fiber, 4 weight portion medical grade nanometer sepiolite fibres mixing ultrasound 3min, supersonic frequency is 300MHz;Again 1 weight portion Aloe extract, 0.5 weight portion Radix et Caulis Opuntiae Dillenii extract, 0.5 weight portion Herba Lysimachiae foenum-graeci quintessence oil are added, continues ultrasound 10min, natural cooling obtain high-performance medicine specific rubber.
Performance detection:
1 to 5 gained finished product of the embodiment of the present invention is carried out into performance test, it is as a result as follows:
Medical grade rubber of the present invention be can be seen that with stronger bending strength and tensile strength from upper table data, it is corrosion-resistant Property it is strong, bactericidal effect is good, with this rubber system for medical supplies, is effective to ensure that drug safety, and market prospect is good, is worth pushing away Extensively.
Embodiment to inventing is explained in detail above, but the invention is not restricted to described embodiment.For For those skilled in the art, in the case of without departing from the principle of the invention and spirit, these embodiments are carried out various Change, modification, replacement and modification, still fall within protection scope of the present invention.

Claims (10)

1. the preparation method of a kind of high-performance medicine specific rubber, it is characterised in that:Comprise the steps:
(1) elastomeric material of clean surface is placed in ultraviolet irradiation reactor, irradiation wavelengths 100-350nm, exposure time 30- 60s, obtains the rubber of surface active;
(2) surfactant solution of 2wt%-5wt% is prepared, surface work after the rubber pulverizing that step (1) is obtained, is added to Property agent solution, be heated to 60-80 DEG C of stirring reaction 10-20min, add benzalkonium chloride, fluorination tributyl tin, ketopyrrolidine carboxylic Sour potassium and antioxidant, are heated to 80-120 DEG C, stirring reaction 5-15min, and deionized water filtration drying obtains compound;
(3), in the compound input ultrasonic reactor for obtaining step (2), Graphene, nano inorganic fiber mixing ultrasound are added 2-5min, adds Extracts from Plant Recourses, Herba Lysimachiae foenum-graeci quintessence oil, continues ultrasound 5-15min, and it is extraordinary that natural cooling obtains high-performance medicine Rubber.
2. the preparation method of high-performance according to claim 1 medicine specific rubber, it is characterised in that:The rubber is doctor With one or more mixture in natural rubber, silicone rubber, isoprene rubber, nitrile rubber, butadiene-styrene rubber.
3. the preparation method of high-performance according to claim 1 medicine specific rubber, it is characterised in that:The surface is modified Agent is polyvinylpyrrolidone, shitosan, sodium alginate, one or more mixture in methoxypolyethylene glycol acrylate.
4. the preparation method of high-performance according to claim 1 medicine specific rubber, it is characterised in that:The Graphene is The graphene oxide obtained after concentrated sulphuric acid acidification.
5. the preparation method of high-performance according to claim 1 medicine specific rubber, it is characterised in that:The nano inorganic Fiber is medical grade gypsum fiber, wollastonite fibre, sepiolite fibre, one or more mixture in brucite fiber.
6. the preparation method of high-performance according to claim 1 medicine specific rubber, it is characterised in that:The plant source is carried Take thing for natural plants are size-reduced, it is the blending that adds water, standings, multiple filtration, concentrated in vacuo, spray drying acquisition.
7. the preparation method of high-performance according to claim 6 medicine specific rubber, it is characterised in that:The natural plants For one or more mixture in Aloe, Herba Menthae, Bulbus Allii, Radix Sophorae Flavescentiss, Radix et Caulis Opuntiae Dillenii.
8. the preparation method of high-performance according to claim 1 medicine specific rubber, it is characterised in that:The step (2) In each parts by weight of raw materials composition:Rubber 50-80 parts, surfactant 10-20 parts, benzalkonium chloride 10-15 parts, fluorination tributyl tin 8-12 parts, 2-pyrrolidone-5-carboxylic acid's potassium 6-10 parts, antioxidant 5-10 parts.
9. the preparation method of high-performance according to claim 1 medicine specific rubber, it is characterised in that:The step (3) In each parts by weight of raw materials composition:Graphene 3-8 parts, nano inorganic fiber 2-10 parts, Extracts from Plant Recourses 1-3 parts, lavandula angustifolia essence Oily 0.5-2 parts.
10. the preparation method of high-performance according to claim 1 medicine specific rubber, it is characterised in that:The step (3) Middle supersonic frequency is 200-300MHz.
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Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN107312188A (en) * 2017-08-02 2017-11-03 四川大学 A kind of porous silicone rubber film of graphene-containing and its production and use
CN107573545A (en) * 2017-07-28 2018-01-12 安徽众康药业有限公司 Far infrared plaster for dispersing swelling matrix of subsensitivety and preparation method thereof
CN112266504A (en) * 2020-09-18 2021-01-26 河北橡一医药科技股份有限公司 Medical rubber and preparation method thereof
CN112812381A (en) * 2020-12-28 2021-05-18 河北橡一医药科技股份有限公司 Medical special rubber and preparation method thereof

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CN101974174A (en) * 2010-10-22 2011-02-16 中国热带农业科学院农产品加工研究所 Method for preparing sterilization and inflammation reducing condom containing natural aloe extract
CN104497372A (en) * 2014-12-23 2015-04-08 青岛科技大学 Clean sterile high-barrier medical rubber plug and preparation method thereof
CN104721875A (en) * 2015-03-18 2015-06-24 华南理工大学 Hydrophilic silicone rubber wound dressing and preparation method thereof
CN105778185A (en) * 2016-03-22 2016-07-20 镇江华扬乳胶制品有限公司 High-strength high-elongation antibacterial soft graphene rubber latex

Patent Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN101974174A (en) * 2010-10-22 2011-02-16 中国热带农业科学院农产品加工研究所 Method for preparing sterilization and inflammation reducing condom containing natural aloe extract
CN104497372A (en) * 2014-12-23 2015-04-08 青岛科技大学 Clean sterile high-barrier medical rubber plug and preparation method thereof
CN104721875A (en) * 2015-03-18 2015-06-24 华南理工大学 Hydrophilic silicone rubber wound dressing and preparation method thereof
CN105778185A (en) * 2016-03-22 2016-07-20 镇江华扬乳胶制品有限公司 High-strength high-elongation antibacterial soft graphene rubber latex

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN107573545A (en) * 2017-07-28 2018-01-12 安徽众康药业有限公司 Far infrared plaster for dispersing swelling matrix of subsensitivety and preparation method thereof
CN107312188A (en) * 2017-08-02 2017-11-03 四川大学 A kind of porous silicone rubber film of graphene-containing and its production and use
CN112266504A (en) * 2020-09-18 2021-01-26 河北橡一医药科技股份有限公司 Medical rubber and preparation method thereof
CN112812381A (en) * 2020-12-28 2021-05-18 河北橡一医药科技股份有限公司 Medical special rubber and preparation method thereof

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