CN106039397B - The preparation method of vitreous carbon, artificial trachea - Google Patents

The preparation method of vitreous carbon, artificial trachea Download PDF

Info

Publication number
CN106039397B
CN106039397B CN201610310581.8A CN201610310581A CN106039397B CN 106039397 B CN106039397 B CN 106039397B CN 201610310581 A CN201610310581 A CN 201610310581A CN 106039397 B CN106039397 B CN 106039397B
Authority
CN
China
Prior art keywords
parts
vitreous carbon
polyacrylonitrile
titanium dioxide
preparation
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.)
Active
Application number
CN201610310581.8A
Other languages
Chinese (zh)
Other versions
CN106039397A (en
Inventor
不公告发明人
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Xionghua Heyuan Optical Technology Co ltd
Original Assignee
Heyuan Longxin Optical Technology Co Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Heyuan Longxin Optical Technology Co Ltd filed Critical Heyuan Longxin Optical Technology Co Ltd
Priority to CN201610310581.8A priority Critical patent/CN106039397B/en
Publication of CN106039397A publication Critical patent/CN106039397A/en
Application granted granted Critical
Publication of CN106039397B publication Critical patent/CN106039397B/en
Active legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Classifications

    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61LMETHODS OR APPARATUS FOR STERILISING MATERIALS OR OBJECTS IN GENERAL; DISINFECTION, STERILISATION OR DEODORISATION OF AIR; CHEMICAL ASPECTS OF BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES; MATERIALS FOR BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES
    • A61L27/00Materials for grafts or prostheses or for coating grafts or prostheses
    • A61L27/02Inorganic materials
    • A61L27/08Carbon ; Graphite
    • CCHEMISTRY; METALLURGY
    • C04CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04BLIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B35/00Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products
    • C04B35/515Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products based on non-oxide ceramics
    • C04B35/52Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products based on non-oxide ceramics based on carbon, e.g. graphite
    • C04B35/524Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products based on non-oxide ceramics based on carbon, e.g. graphite obtained from polymer precursors, e.g. glass-like carbon material
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61FFILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
    • A61F2/00Filters implantable into blood vessels; Prostheses, i.e. artificial substitutes or replacements for parts of the body; Appliances for connecting them with the body; Devices providing patency to, or preventing collapsing of, tubular structures of the body, e.g. stents
    • A61F2/02Prostheses implantable into the body
    • A61F2/04Hollow or tubular parts of organs, e.g. bladders, tracheae, bronchi or bile ducts
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61LMETHODS OR APPARATUS FOR STERILISING MATERIALS OR OBJECTS IN GENERAL; DISINFECTION, STERILISATION OR DEODORISATION OF AIR; CHEMICAL ASPECTS OF BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES; MATERIALS FOR BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES
    • A61L27/00Materials for grafts or prostheses or for coating grafts or prostheses
    • A61L27/02Inorganic materials
    • A61L27/10Ceramics or glasses
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61LMETHODS OR APPARATUS FOR STERILISING MATERIALS OR OBJECTS IN GENERAL; DISINFECTION, STERILISATION OR DEODORISATION OF AIR; CHEMICAL ASPECTS OF BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES; MATERIALS FOR BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES
    • A61L27/00Materials for grafts or prostheses or for coating grafts or prostheses
    • A61L27/50Materials characterised by their function or physical properties, e.g. injectable or lubricating compositions, shape-memory materials, surface modified materials
    • CCHEMISTRY; METALLURGY
    • C04CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04BLIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B35/00Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products
    • C04B35/622Forming processes; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61FFILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
    • A61F2/00Filters implantable into blood vessels; Prostheses, i.e. artificial substitutes or replacements for parts of the body; Appliances for connecting them with the body; Devices providing patency to, or preventing collapsing of, tubular structures of the body, e.g. stents
    • A61F2/02Prostheses implantable into the body
    • A61F2/04Hollow or tubular parts of organs, e.g. bladders, tracheae, bronchi or bile ducts
    • A61F2002/046Tracheae
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61LMETHODS OR APPARATUS FOR STERILISING MATERIALS OR OBJECTS IN GENERAL; DISINFECTION, STERILISATION OR DEODORISATION OF AIR; CHEMICAL ASPECTS OF BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES; MATERIALS FOR BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES
    • A61L2430/00Materials or treatment for tissue regeneration
    • A61L2430/22Materials or treatment for tissue regeneration for reconstruction of hollow organs, e.g. bladder, esophagus, urether, uterus
    • CCHEMISTRY; METALLURGY
    • C04CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04BLIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B2235/00Aspects relating to ceramic starting mixtures or sintered ceramic products
    • C04B2235/02Composition of constituents of the starting material or of secondary phases of the final product
    • C04B2235/30Constituents and secondary phases not being of a fibrous nature
    • C04B2235/32Metal oxides, mixed metal oxides, or oxide-forming salts thereof, e.g. carbonates, nitrates, (oxy)hydroxides, chlorides
    • C04B2235/3201Alkali metal oxides or oxide-forming salts thereof
    • CCHEMISTRY; METALLURGY
    • C04CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04BLIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B2235/00Aspects relating to ceramic starting mixtures or sintered ceramic products
    • C04B2235/02Composition of constituents of the starting material or of secondary phases of the final product
    • C04B2235/30Constituents and secondary phases not being of a fibrous nature
    • C04B2235/32Metal oxides, mixed metal oxides, or oxide-forming salts thereof, e.g. carbonates, nitrates, (oxy)hydroxides, chlorides
    • C04B2235/3205Alkaline earth oxides or oxide forming salts thereof, e.g. beryllium oxide
    • C04B2235/3208Calcium oxide or oxide-forming salts thereof, e.g. lime
    • C04B2235/3212Calcium phosphates, e.g. hydroxyapatite
    • CCHEMISTRY; METALLURGY
    • C04CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04BLIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B2235/00Aspects relating to ceramic starting mixtures or sintered ceramic products
    • C04B2235/02Composition of constituents of the starting material or of secondary phases of the final product
    • C04B2235/30Constituents and secondary phases not being of a fibrous nature
    • C04B2235/32Metal oxides, mixed metal oxides, or oxide-forming salts thereof, e.g. carbonates, nitrates, (oxy)hydroxides, chlorides
    • C04B2235/3231Refractory metal oxides, their mixed metal oxides, or oxide-forming salts thereof
    • C04B2235/3232Titanium oxides or titanates, e.g. rutile or anatase
    • CCHEMISTRY; METALLURGY
    • C04CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04BLIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B2235/00Aspects relating to ceramic starting mixtures or sintered ceramic products
    • C04B2235/02Composition of constituents of the starting material or of secondary phases of the final product
    • C04B2235/30Constituents and secondary phases not being of a fibrous nature
    • C04B2235/48Organic compounds becoming part of a ceramic after heat treatment, e.g. carbonising phenol resins
    • CCHEMISTRY; METALLURGY
    • C04CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04BLIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B2235/00Aspects relating to ceramic starting mixtures or sintered ceramic products
    • C04B2235/02Composition of constituents of the starting material or of secondary phases of the final product
    • C04B2235/50Constituents or additives of the starting mixture chosen for their shape or used because of their shape or their physical appearance
    • C04B2235/54Particle size related information
    • C04B2235/5418Particle size related information expressed by the size of the particles or aggregates thereof
    • C04B2235/5427Particle size related information expressed by the size of the particles or aggregates thereof millimeter or submillimeter sized, i.e. larger than 0,1 mm
    • CCHEMISTRY; METALLURGY
    • C04CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04BLIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B2235/00Aspects relating to ceramic starting mixtures or sintered ceramic products
    • C04B2235/02Composition of constituents of the starting material or of secondary phases of the final product
    • C04B2235/50Constituents or additives of the starting mixture chosen for their shape or used because of their shape or their physical appearance
    • C04B2235/54Particle size related information
    • C04B2235/5418Particle size related information expressed by the size of the particles or aggregates thereof
    • C04B2235/5436Particle size related information expressed by the size of the particles or aggregates thereof micrometer sized, i.e. from 1 to 100 micron
    • CCHEMISTRY; METALLURGY
    • C04CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04BLIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B2235/00Aspects relating to ceramic starting mixtures or sintered ceramic products
    • C04B2235/70Aspects relating to sintered or melt-casted ceramic products
    • C04B2235/96Properties of ceramic products, e.g. mechanical properties such as strength, toughness, wear resistance

Abstract

The invention discloses the preparation method of vitreous carbon, artificial trachea, the vitreous carbon by artificial trachea includes the raw material based on following parts by weight: 40 ~ 100 parts of polyacrylonitrile, 30 ~ 40 parts of polysiloxanes, 80 ~ 100 parts of cellulose acetate, 20 ~ 30 parts of polyvinyl chloride, 10 ~ 20 parts of tricalcium phosphate, 90 ~ 100 parts of potassium oxide, 20 ~ 70 parts of titanium dioxide, 60 ~ 90 parts of dimethyl silicone polymer.Preparation method: polyacrylonitrile, polysiloxanes, cellulose acetate, polyvinyl chloride, tricalcium phosphate, potassium oxide, titanium dioxide, dimethyl silicone polymer are uniformly mixed, and are melted, and are cooled and shaped;Carbonization treatment is carried out in no oxygen medium, then heats to 2000 ~ 3000 DEG C of 1 ~ 2h of reaction.Vitreous carbon biological stability of the invention is preferable, and elasticity modulus is 22 ~ 24GPa, and fatigue strength is 93 ~ 100MPa, and compression strength is 680 ~ 700MPa, and resistance to biodeterioration can be strong.

Description

The preparation method of vitreous carbon, artificial trachea
Technical field
The present invention relates to biological medicine Material Fields more particularly to a kind of for the vitreous carbon of artificial trachea and its preparation side Method.
Background technique
Vitreous carbon (GC) is a kind of novel carbon material vitreous carbon, small with air-tightness and good conductivity, coefficient of thermal expansion, The features such as quality is hard and is easily polished into mirror surface, chemical inertness, hydrogen overpotential with higher, therefore be suitable for doing electrochemistry With the working electrode material of electroanalysis.It is referred to as vitreous carbon because of its port pattern glass similar with structure feature, is 1962 Year has almost been invented simultaneously by the Davison and Japan Yamada of Britain.Since vitreous carbon has, density is small, high temperature resistant, anti- The characteristics such as infiltration, make it have been widely used in numerous areas such as chemical industry, metallurgical industry, electronics industry, bioengineering.
Vitreous carbon is with air-tightness and good conductivity, coefficient of thermal expansion are small, quality is hard and it is lazy to be easily polished into mirror surface, chemistry Property, hydrogen overpotential with higher the features such as, therefore be suitable for doing the working electrode material of electrochemistry and electroanalysis.Electrode Form has rodlike, disk, rotating circular disk, rotating ring disk electrode (r.r.d.e) etc..The applicable potential range of glassy carbon electrode is wider, both can be Inorganic matter is studied in negative potential area, can also study the redox reaction of the organic matter mostly occurred in positive potential area.Make base with it Body can also prepare mercury membrane glass-carbon electrode and chemically modified electrode.Electrode to be carried out before use surface polishing, chemical treatment and Electrochemical treatments.
Summary of the invention
The vitreous carbon and preparation method thereof that in view of the deficiencies of the prior art, the present invention provides a kind of for artificial trachea, glass Glass carbon resistance to biodeterioration can be strong.
In order to solve the above-mentioned technical problem, the invention adopts the following technical scheme:
For the vitreous carbon of artificial trachea, the raw material including following parts by weight meter: 40~100 parts of polyacrylonitrile, poly- silicon oxygen 30~40 parts of alkane, 80~100 parts of cellulose acetate, 20~30 parts of polyvinyl chloride, 10~20 parts of tricalcium phosphate, potassium oxide 90~ 100 parts, 20~70 parts of titanium dioxide, 60~90 parts of dimethyl silicone polymer.
As a further refinement of the present invention, it is used for the vitreous carbon of artificial trachea, the raw material including following parts by weight meter: 70 parts of polyacrylonitrile, 35 parts of polysiloxanes, 90 parts of cellulose acetate, 25 parts of polyvinyl chloride, 15 parts of tricalcium phosphate, potassium oxide 95 Part, 50 parts of titanium dioxide, 70 parts of dimethyl silicone polymer.
As a further refinement of the present invention, the partial size of titanium dioxide is 40~150 μm.
As a further refinement of the present invention, the molecular weight of polyacrylonitrile is 10000~20000.
The present invention also provides a kind of preparation methods of vitreous carbon for artificial trachea.
A kind of preparation method of the vitreous carbon for artificial trachea, comprising the following steps: polyacrylonitrile, polysiloxanes, vinegar Acid cellulose, polyvinyl chloride, tricalcium phosphate, potassium oxide, titanium dioxide, dimethyl silicone polymer are uniformly mixed, and fusing is cooled to Type;Carbonization treatment is carried out in no oxygen medium, then heats to 2000~3000 DEG C of 1~2h of reaction, and the carbonization treatment time is 20 ~50min.
A kind of artificial trachea uses above-mentioned vitreous carbon to be made.
The utility model has the advantages that the vitreous carbon of the prior art due to bioenvironmental corrosion cause wherein metal ion to surrounding tissue Diffusion, vitreous carbon of the invention can be used as artificial trachea application, not perishable diffusion, be the glass because after carbonization treatment Carbon biological stability is preferable, elasticity modulus be 22~24GPa, fatigue strength be 93~100MPa, compression strength be 680~ 700MPa, resistance to biodeterioration can be strong.
Specific embodiment
The present invention is further explained in the light of specific embodiments.
Embodiment 1
For the vitreous carbon of artificial trachea, the raw material including following parts by weight meter: 70 parts of polyacrylonitrile, polysiloxanes 35 Part, 90 parts of cellulose acetate, 25 parts of polyvinyl chloride, 15 parts of tricalcium phosphate, 95 parts of potassium oxide, 50 parts of titanium dioxide, poly dimethyl 70 parts of siloxanes.
The partial size of titanium dioxide is 100 μm.
The molecular weight of polyacrylonitrile is 15000.
A kind of preparation method of the vitreous carbon for artificial trachea, comprising the following steps: polyacrylonitrile, polysiloxanes, vinegar Acid cellulose, polyvinyl chloride, tricalcium phosphate, potassium oxide, titanium dioxide, dimethyl silicone polymer are uniformly mixed, and fusing is cooled to Type;Carbonization treatment is carried out in no oxygen medium, then heats to 2500 DEG C of reaction 1.5h.
The carbonization treatment time is 40min.
Embodiment 2
For the vitreous carbon of artificial trachea, the raw material including following parts by weight meter: 40 parts of polyacrylonitrile, polysiloxanes 30 Part, 80 parts of cellulose acetate, 20 parts of polyvinyl chloride, 10 parts of tricalcium phosphate, 90 parts of potassium oxide, 20 parts of titanium dioxide, poly dimethyl 60 parts of siloxanes.
The partial size of titanium dioxide is 40 μm.
The molecular weight of polyacrylonitrile is 10000.
A kind of preparation method of the vitreous carbon for artificial trachea, comprising the following steps: polyacrylonitrile, polysiloxanes, vinegar Acid cellulose, polyvinyl chloride, tricalcium phosphate, potassium oxide, titanium dioxide, dimethyl silicone polymer are uniformly mixed, and fusing is cooled to Type;Carbonization treatment is carried out in no oxygen medium, then heats to 2000 DEG C of reaction 1h.
The carbonization treatment time is 20min.
Embodiment 3
For the vitreous carbon of artificial trachea, the raw material including following parts by weight meter: 100 parts of polyacrylonitrile, polysiloxanes 40 Part, 100 parts of cellulose acetate, 30 parts of polyvinyl chloride, 20 parts of tricalcium phosphate, 100 parts of potassium oxide, 70 parts of titanium dioxide, poly- diformazan 90 parts of radical siloxane.
The partial size of titanium dioxide is 150 μm.
The molecular weight of polyacrylonitrile is 20000.
A kind of preparation method of the vitreous carbon for artificial trachea, comprising the following steps: polyacrylonitrile, polysiloxanes, vinegar Acid cellulose, polyvinyl chloride, tricalcium phosphate, potassium oxide, titanium dioxide, dimethyl silicone polymer are uniformly mixed, and fusing is cooled to Type;Carbonization treatment is carried out in no oxygen medium, then heats to 3000 DEG C of reaction 2h.
The carbonization treatment time is 50min.
Embodiment 4
For the vitreous carbon of artificial trachea, the raw material including following parts by weight meter: 90 parts of polyacrylonitrile, polysiloxanes 33 Part, 85 parts of cellulose acetate, 22 parts of polyvinyl chloride, 12 parts of tricalcium phosphate, 93 parts of potassium oxide, 30 parts of titanium dioxide, poly dimethyl 70 parts of siloxanes.
The partial size of titanium dioxide is 60 μm.
The molecular weight of polyacrylonitrile is 12000.
A kind of preparation method of the vitreous carbon for artificial trachea, comprising the following steps: polyacrylonitrile, polysiloxanes, vinegar Acid cellulose, polyvinyl chloride, tricalcium phosphate, potassium oxide, titanium dioxide, dimethyl silicone polymer are uniformly mixed, and fusing is cooled to Type;Carbonization treatment is carried out in no oxygen medium, then heats to 2200 DEG C of reaction 1.2h.
The carbonization treatment time is 25min.
Embodiment 5
For the vitreous carbon of artificial trachea, the raw material including following parts by weight meter: 80 parts of polyacrylonitrile, polysiloxanes 38 Part, 97 parts of cellulose acetate, 28 parts of polyvinyl chloride, 18 parts of tricalcium phosphate, 98 parts of potassium oxide, 60 parts of titanium dioxide, poly dimethyl 80 parts of siloxanes.
The partial size of titanium dioxide is 130 μm.
The molecular weight of polyacrylonitrile is 18000.
A kind of preparation method of the vitreous carbon for artificial trachea, comprising the following steps: polyacrylonitrile, polysiloxanes, vinegar Acid cellulose, polyvinyl chloride, tricalcium phosphate, potassium oxide, titanium dioxide, dimethyl silicone polymer are uniformly mixed, and fusing is cooled to Type;Carbonization treatment is carried out in no oxygen medium, then heats to 2800 DEG C of reaction 1.8h.
The carbonization treatment time is 40min.
Comparative example 1
Same as Example 1, difference is: being omitted in no oxygen medium the step of carrying out carbonization treatment.
Performance test
The properties of product for measuring embodiment and comparative example, the results are shown in Table 1.
Table 1
Conclusion: the vitreous carbon biological stability after carbonization treatment is preferable, will not be as the vitreous carbon of the prior art is due to life The corrosion of substance environment cause wherein metal ion to surrounding tissue spread, vitreous carbon elasticity modulus of the invention be 22~24GPa, Fatigue strength is 93~100MPa, and compression strength is 680~700MPa, and resistance to biodeterioration can be strong.

Claims (2)

1. for artificial trachea vitreous carbon preparation method, which is characterized in that vitreous carbon by following parts by weight meter raw material group At: 40~100 parts of polyacrylonitrile, 30~40 parts of polysiloxanes, 80~100 parts of cellulose acetate, 20~30 parts of polyvinyl chloride, phosphorus 10~20 parts of sour tricalcium, 90~100 parts of potassium oxide, 20~70 parts of titanium dioxide, 60~90 parts of dimethyl silicone polymer;
The partial size of titanium dioxide is 40~150 μm;
The molecular weight of polyacrylonitrile is 10000~20000;
The preparation method, comprising the following steps: polyacrylonitrile, polysiloxanes, cellulose acetate, polyvinyl chloride, tricresyl phosphate Calcium, potassium oxide, titanium dioxide, dimethyl silicone polymer are uniformly mixed, and are melted, and are cooled and shaped;It is carbonized in no oxygen medium Processing, then heats to 2000~3000 DEG C of 1~2h of reaction;The carbonization treatment time is 20~50min.
2. a kind of artificial trachea, which is characterized in that it uses vitreous carbon made from preparation method described in claim 1.
CN201610310581.8A 2014-11-10 2014-11-10 The preparation method of vitreous carbon, artificial trachea Active CN106039397B (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN201610310581.8A CN106039397B (en) 2014-11-10 2014-11-10 The preparation method of vitreous carbon, artificial trachea

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
CN201410625934.4A CN104445142B (en) 2014-11-10 2014-11-10 Vitreous carbon for artificial trachea and preparation method thereof
CN201610310581.8A CN106039397B (en) 2014-11-10 2014-11-10 The preparation method of vitreous carbon, artificial trachea

Related Parent Applications (1)

Application Number Title Priority Date Filing Date
CN201410625934.4A Division CN104445142B (en) 2014-11-10 2014-11-10 Vitreous carbon for artificial trachea and preparation method thereof

Publications (2)

Publication Number Publication Date
CN106039397A CN106039397A (en) 2016-10-26
CN106039397B true CN106039397B (en) 2019-05-17

Family

ID=52892006

Family Applications (7)

Application Number Title Priority Date Filing Date
CN201610310549.XA Expired - Fee Related CN105948749B (en) 2014-11-10 2014-11-10 The preparation method of the strong vitreous carbon of resistance to biodeterioration energy, artificial trachea
CN201610310581.8A Active CN106039397B (en) 2014-11-10 2014-11-10 The preparation method of vitreous carbon, artificial trachea
CN201610310548.5A Active CN106007719B (en) 2014-11-10 2014-11-10 A kind of preparation method of the strong vitreous carbon of resistance to biodeterioration energy, artificial trachea
CN201610312351.5A Expired - Fee Related CN105999395B (en) 2014-11-10 2014-11-10 A kind of preparation method of vitreous carbon, artificial trachea
CN201610312249.5A Active CN105948750B (en) 2014-11-10 2014-11-10 Vitreous carbon and its manufactured artificial trachea
CN201610312354.9A Active CN105859293B (en) 2014-11-10 2014-11-10 Vitreous carbon and its manufactured artificial trachea for artificial trachea
CN201410625934.4A Active CN104445142B (en) 2014-11-10 2014-11-10 Vitreous carbon for artificial trachea and preparation method thereof

Family Applications Before (1)

Application Number Title Priority Date Filing Date
CN201610310549.XA Expired - Fee Related CN105948749B (en) 2014-11-10 2014-11-10 The preparation method of the strong vitreous carbon of resistance to biodeterioration energy, artificial trachea

Family Applications After (5)

Application Number Title Priority Date Filing Date
CN201610310548.5A Active CN106007719B (en) 2014-11-10 2014-11-10 A kind of preparation method of the strong vitreous carbon of resistance to biodeterioration energy, artificial trachea
CN201610312351.5A Expired - Fee Related CN105999395B (en) 2014-11-10 2014-11-10 A kind of preparation method of vitreous carbon, artificial trachea
CN201610312249.5A Active CN105948750B (en) 2014-11-10 2014-11-10 Vitreous carbon and its manufactured artificial trachea
CN201610312354.9A Active CN105859293B (en) 2014-11-10 2014-11-10 Vitreous carbon and its manufactured artificial trachea for artificial trachea
CN201410625934.4A Active CN104445142B (en) 2014-11-10 2014-11-10 Vitreous carbon for artificial trachea and preparation method thereof

Country Status (1)

Country Link
CN (7) CN105948749B (en)

Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN101626075A (en) * 2009-08-03 2010-01-13 北京化工大学 Stannum and carbon composite nano-fiber film negative-electrode material and preparation method thereof
CN102168324A (en) * 2011-03-08 2011-08-31 西安工程大学 Carbonization device for electrostatically spinning nanometer tows and preparation method of carbon nanofibers

Family Cites Families (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP3548649B2 (en) * 1996-03-26 2004-07-28 東海カーボン株式会社 Carbon heating element
EP0858968B1 (en) * 1996-08-28 2001-12-12 Nisshinbo Industries, Inc. Glassy carbon and process for the preparation thereof
JP2005326240A (en) * 2004-05-13 2005-11-24 Toshiba Corp Analyzing container and method for analyzing very small amount of element
EP2570385A3 (en) * 2005-05-03 2013-10-16 Nanocomp Technologies, Inc. Carbon composite materials and methods of manufacturing same
CN104528693B (en) * 2009-05-26 2017-05-10 创业发展联盟技术有限公司 Carbon material and method for producing the same
JP2013500922A (en) * 2009-07-31 2013-01-10 マサチューセッツ インスティテュート オブ テクノロジー Systems and methods for the formation of carbon-based nanostructures
CN102276280A (en) * 2011-04-20 2011-12-14 上海交通大学 Vitreous carbon and carbon additive based composite thin plate and preparation method thereof
CN102936763B (en) * 2012-10-12 2015-03-18 福建师范大学 Glass carbon nanometer fiber preparation method
CN103508437A (en) * 2013-08-13 2014-01-15 南京工业大学 Preparation method of phenolic resin base glass carbon microsphere

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN101626075A (en) * 2009-08-03 2010-01-13 北京化工大学 Stannum and carbon composite nano-fiber film negative-electrode material and preparation method thereof
CN102168324A (en) * 2011-03-08 2011-08-31 西安工程大学 Carbonization device for electrostatically spinning nanometer tows and preparation method of carbon nanofibers

Also Published As

Publication number Publication date
CN106007719B (en) 2018-06-29
CN105999395B (en) 2019-01-01
CN105948749A (en) 2016-09-21
CN105859293B (en) 2018-06-29
CN105948750B (en) 2018-08-10
CN105999395A (en) 2016-10-12
CN105948749B (en) 2018-06-29
CN104445142B (en) 2016-11-23
CN105948750A (en) 2016-09-21
CN106039397A (en) 2016-10-26
CN106007719A (en) 2016-10-12
CN105859293A (en) 2016-08-17
CN104445142A (en) 2015-03-25

Similar Documents

Publication Publication Date Title
CN105523541B (en) Porous carbon tiny balloon of Heteroatom doping and preparation method thereof
Lian et al. Boron nitride ultrathin fibrous nanonets: one-step synthesis and applications for ultrafast adsorption for water treatment and selective filtration of nanoparticles
KR101826585B1 (en) Nitrogen-doped graphene aggregate and method of preparing the same
CN107449816B (en) All solid state ion selective electrode, preparation method and biosensor
Li et al. A catechol biosensor based on electrospun carbon nanofibers
CN106542517A (en) The preparation method of carbon aerogels
Liu et al. A metal-catalyst free, flexible and free-standing chitosan/vacuum-stripped graphene/polypyrrole three dimensional electrode interface for high performance dopamine sensing
Li et al. Comparative study on the anodizing process of Ti and Zr and oxide morphology
KR20170124591A (en) Activated carbon having basic functional groups and method for producing same
CN109761216A (en) A kind of general, method that porous carbon materials are prepared based on organic zinc salt
CN110451490A (en) A kind of preparation method of porous graphene material
Cheong et al. Ultralight, structurally stable electrospun sponges with tailored hydrophilicity as a novel material platform
CN106039397B (en) The preparation method of vitreous carbon, artificial trachea
CN105800589B (en) A kind of vitreous carbon and its manufactured artificial trachea
CN105399086B (en) A kind of method that sodium chloride auxiliary prepares graphene perforated membrane
CN104627995B (en) Bubbly graphene material and preparation method thereof
CN111855772A (en) Porous carbon modified glassy carbon electrode and electrochemical method for detecting three targets
CN114261955B (en) Gelidium amansii derived tri-carbon tetranitride/porous graphitized carbon as well as preparation method and application thereof
KR20190086290A (en) Biosorbent and a method for continosuly recovering lithum using the same
CN108448164A (en) Sode cell based on self-supporting fluorine nitrogen-doped graphene film
Periyasamy et al. Innovative Carbon Ball Frameworks: Elevating Energy Storage Performance and Enhancing CO2 Capture Efficiency
TW201533937A (en) Flexible thermoelectric material film and manufacturing method thereof
Mohanty et al. Conducting pyrolysed carbon scaffold for tissue engineering
WANG et al. DNA-nano-porous hydroxyapatite modified electrode applied to the study on the interactions of DNA with methylene blue
CN104177637A (en) Preparation method of sulfur-doped polyaniline and titanium dioxide composite nanowire gas-sensitive film with mercury sensing response

Legal Events

Date Code Title Description
C06 Publication
PB01 Publication
C10 Entry into substantive examination
SE01 Entry into force of request for substantive examination
TA01 Transfer of patent application right
TA01 Transfer of patent application right

Effective date of registration: 20190417

Address after: 517000 Building E of Xionghua Science and Technology Park, No. 1 Xingye Avenue, Heyuan High-tech Zone, Guangdong Province

Applicant after: Heyuan Longxin Optical Technology Co.,Ltd.

Address before: 213000 Jinling North Road, Xinbei District, Changzhou, Jiangsu, China, Hohai University

Applicant before: Wu Jie

GR01 Patent grant
GR01 Patent grant
CP01 Change in the name or title of a patent holder
CP01 Change in the name or title of a patent holder

Address after: 517000 Building E of Xionghua Science and Technology Park, No. 1 Xingye Avenue, Heyuan High-tech Zone, Guangdong Province

Patentee after: Xionghua (Heyuan) Optical Technology Co.,Ltd.

Address before: 517000 Building E of Xionghua Science and Technology Park, No. 1 Xingye Avenue, Heyuan High-tech Zone, Guangdong Province

Patentee before: Heyuan Longxin Optical Technology Co.,Ltd.