CN101224309A - Macromolecule bandage and fabricating method thereof - Google Patents
Macromolecule bandage and fabricating method thereof Download PDFInfo
- Publication number
- CN101224309A CN101224309A CNA200710302502XA CN200710302502A CN101224309A CN 101224309 A CN101224309 A CN 101224309A CN A200710302502X A CNA200710302502X A CN A200710302502XA CN 200710302502 A CN200710302502 A CN 200710302502A CN 101224309 A CN101224309 A CN 101224309A
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- fat
- bandage
- reactor
- isocyanide
- grams
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Abstract
The invention discloses a macromolecule bandage which consists of bandage substrates and medical adhesive that is coated on the bandage substrates. The invention is characterized in that the raw materials of the medical adhesive consists of trichloroisocyanuric lipid, polyether, di-n-butyl phthalate, methyl silicone oil, polyethylene glycols stearic diester, methanesulfonic acid and di-morpholine diethyl ether; the materials react to generate the medical adhesive which is coated on a polyester fiber belt and the nitrogen is pumped in for packaging and sealing. Compared with the existent medical bandage, the invention has the advantages of short solidification time, high intensity, easy bandage removal and good perspective effect under x rays.
Description
Technical field
The invention belongs to a kind of medical and hygiene article, specifically is a kind of medical bandage and preparation method thereof.
Background technology
Medical bandage is widely used in traumatology patient wrapping, helps knochenbruch rectification etc.Existing medical bandage exists intensity low, easily gets loose, and hardening time is long, and production efficiency is lower, and bone injury patient is when carrying out x-ray bombardment, and binder easily causes interference.
Summary of the invention
The purpose of this invention is to provide a kind of AGMA and preparation method thereof, this medical bandage intensity height is difficult for getting loose, and hardening time is short, and readily removable removing is better than like product transparent effect under X ray.
Technical scheme of the present invention is as follows:
A kind of AGMA is made up of binder base material and the medical glue that is coated on the binder base material, it is characterized in that described medical collagen material proportioning is:
Isocyanide fat 8-12 kilogram
Polyethers 4-8 kilogram
Dibutyl phthalate 160-240 milliliter
Methyl-silicone oil 15-25 gram
The two hard acid fat 450-520 grams of Polyethylene Glycol
Loprazolam 40-60 gram
Dual-morpholinyl diethyl ether 350-390 milliliter.
Described a kind of AGMA is characterized in that described medical collagen material proportioning is:
10 kilograms in isocyanide fat
6 kilograms of polyethers
200 milliliters of dibutyl phthalates
Methyl-silicone oil 20 grams
Two hard acid fat 480 grams of Polyethylene Glycol
Loprazolam 50 grams
370 milliliters of dual-morpholinyl diethyl ethers.
The preparation method of described AGMA is characterized in that may further comprise the steps:
(1) binder base material dacron thread is drying;
(2) isocyanide fat being put into reactor heats to 40-50 ℃;
(3) Loprazolam is added fully stirring in the methyl-silicone oil, added reactor and isocyanide fat complete reaction then;
(4) dibutyl phthalate and the two hard acid fat of Polyethylene Glycol are added complete reaction in the reactor respectively, again the polyethers point is added dropwise in the reactor, fully stirred 2-4 hour after after 1 hour temperature of reaction kettle being raised to 75-85 ℃ of insulation, temperature of reaction kettle is reduced to 50-60 ℃ then, continues stirring reaction;
(5) add dual-morpholinyl diethyl ether, stir, obtain described medical glue, temperature is controlled at about 45-55 ℃, and nitrogen is filled in the reactor sealing;
(6) on the binder base material terylene silk ribbon of oven dry, be coated with described medical glue;
(7) towards the nitrogen packaging seal.
Advantage of the present invention:
Shorter hardening time than existing medical bandage, the intensity height, readily removable removing, transparent effect is good under the X line.
The specific embodiment
A kind of AGMA, form the proportioning of medical glue by binder base material and the medical glue that is coated on the binder base material:
10 kilograms in isocyanide fat
6 kilograms of polyethers
200 milliliters of dibutyl phthalates
Methyl-silicone oil 20 grams
Two hard acid fat 480 grams of Polyethylene Glycol
Loprazolam 50 grams
370 milliliters of dual-morpholinyl diethyl ethers
Two, AGMA production technology:
1, puts the terylene silk ribbon into electric baker heating, oven dry 48 hours in the previous day that feeds intake, temperature is controlled at about 85 degrees centigrade feeds intake;
2, binder base material dacron thread is drying;
3, isocyanide fat being put into reactor heats to 50 ℃;
4, Loprazolam is added in the methyl-silicone oil fully to stir and added reactor and isocyanide fat complete reaction in 10 minutes then 30 minutes;
5, the two hard acid fat of dibutyl phthalate and Polyethylene Glycol were added in the reactor complete reaction respectively 45 minutes, again the polyethers point is added dropwise in the reactor, polyethers must be finished by drop in 1 hour, fully stirred 3 hours after after 1 hour temperature of reaction kettle being raised to 80 ℃ of insulations, temperature of reaction kettle is reduced to 55 ℃ then, continues stirring reaction;
6, dual-morpholinyl diethyl ether adds before gluing is produced, and can produce after stirring, and temperature is controlled at about 50 ℃, and nitrogen is filled in the reactor sealing; Earlier with workbench case heating and dehumidification, temperature is controlled at 45-46 ℃ before gluing work, and humidity is controlled at 5%RH--3%RH, can begin operation;
7, gluing on the binder base material terylene silk ribbon of oven dry;
8, towards the nitrogen packaging seal.
9, vanning.
Claims (3)
1. AGMA is made up of binder base material and the medical glue that is coated on the binder base material, it is characterized in that described medical collagen material proportioning is:
Isocyanide fat 8-12 kilogram
Polyethers 4-8 kilogram
Dibutyl phthalate 160-240 milliliter
Methyl-silicone oil 15-25 gram
The two hard acid fat 450-520 grams of Polyethylene Glycol
Loprazolam 40-60 gram
Dual-morpholinyl diethyl ether 350-390 milliliter.
2. a kind of AGMA according to claim 1 is characterized in that described medical collagen material proportioning is:
10 kilograms in isocyanide fat
6 kilograms of polyethers
200 milliliters of dibutyl phthalates
Methyl-silicone oil 20 grams
Two hard acid fat 480 grams of Polyethylene Glycol
Loprazolam 50 grams
370 milliliters of dual-morpholinyl diethyl ethers.
3. the preparation method of AGMA according to claim 1 is characterized in that may further comprise the steps:
(1) binder base material dacron thread is drying;
(2) isocyanide fat being put into reactor heats to 40-50 ℃;
(3) Loprazolam is added fully stirring in the methyl-silicone oil, added reactor and isocyanide fat complete reaction then;
(4) dibutyl phthalate and the two hard acid fat of Polyethylene Glycol are added complete reaction in the reactor respectively, again the polyethers point is added dropwise in the reactor, fully stirred 2-4 hour after after 1 hour temperature of reaction kettle being raised to 75-85 ℃ of insulation, temperature of reaction kettle is reduced to 50-60 ℃ then, continues stirring reaction;
(5) add dual-morpholinyl diethyl ether, stir, obtain described medical glue, temperature is controlled at about 45-55 ℃, and nitrogen is filled in the reactor sealing;
(6) on the binder base material terylene silk ribbon of oven dry, be coated with described medical glue;
(7) towards the nitrogen packaging seal.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CNA200710302502XA CN101224309A (en) | 2007-12-24 | 2007-12-24 | Macromolecule bandage and fabricating method thereof |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CNA200710302502XA CN101224309A (en) | 2007-12-24 | 2007-12-24 | Macromolecule bandage and fabricating method thereof |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CN101224309A true CN101224309A (en) | 2008-07-23 |
Family
ID=39856653
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CNA200710302502XA Pending CN101224309A (en) | 2007-12-24 | 2007-12-24 | Macromolecule bandage and fabricating method thereof |
Country Status (1)
| Country | Link |
|---|---|
| CN (1) | CN101224309A (en) |
Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN104825273A (en) * | 2015-05-30 | 2015-08-12 | 李孟平 | Method for preparing breathable self-adhesion elastic bandage |
| CN105385401A (en) * | 2015-12-26 | 2016-03-09 | 盐城西臣奥勒医疗科技有限公司 | Organic silicone modified polyurethane synthetic adhesive and preparation method thereof |
| CN108404196A (en) * | 2018-03-23 | 2018-08-17 | 安徽三山新材料科技有限公司 | A kind of bandage spraying slurry |
| CN113080573A (en) * | 2021-05-21 | 2021-07-09 | 广州梵骅鞋业发展有限公司 | Method for obtaining foot size through forming shoe mold |
-
2007
- 2007-12-24 CN CNA200710302502XA patent/CN101224309A/en active Pending
Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN104825273A (en) * | 2015-05-30 | 2015-08-12 | 李孟平 | Method for preparing breathable self-adhesion elastic bandage |
| CN105385401A (en) * | 2015-12-26 | 2016-03-09 | 盐城西臣奥勒医疗科技有限公司 | Organic silicone modified polyurethane synthetic adhesive and preparation method thereof |
| CN108404196A (en) * | 2018-03-23 | 2018-08-17 | 安徽三山新材料科技有限公司 | A kind of bandage spraying slurry |
| CN113080573A (en) * | 2021-05-21 | 2021-07-09 | 广州梵骅鞋业发展有限公司 | Method for obtaining foot size through forming shoe mold |
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| C06 | Publication | ||
| PB01 | Publication | ||
| C10 | Entry into substantive examination | ||
| SE01 | Entry into force of request for substantive examination | ||
| C12 | Rejection of a patent application after its publication | ||
| RJ01 | Rejection of invention patent application after publication |
Open date: 20080723 |