CN1323855A - Antibacterial polyurethane material and its prepn. - Google Patents
Antibacterial polyurethane material and its prepn. Download PDFInfo
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- CN1323855A CN1323855A CN 01113420 CN01113420A CN1323855A CN 1323855 A CN1323855 A CN 1323855A CN 01113420 CN01113420 CN 01113420 CN 01113420 A CN01113420 A CN 01113420A CN 1323855 A CN1323855 A CN 1323855A
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- tannin
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- polyvalent alcohol
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Abstract
The present invention relates to polyurethane material possessing antibacterial action. Tannin or bark containing tanning is used as crosslinking agent. Said material not only possesses the performance of common polyurethane, but also possesses stable and durable antibacterial property, it is easy to be degraded and can be used in various fields such as packaging material, shoe sole material, toy material etc.
Description
The invention belongs to technical field of polymer materials, be specifically related to a kind of polyurethane material and preparation method thereof with bacteriostatic action.
Polyurethane material becomes one of the world today's six big synthesized polymer materials owing to its good performance and cheap price, and its annual production surpasses 100,000,000 tons, has been widely used in every field.In recent years, the production year rate of increase of the polyurethane material of China has reached 18%.Along with improving constantly of people's quality of life, proposed to develop the requirement of polyurethane material with anti-microbial effect.But, do not have anti-microbial effect with TriMethylolPropane(TMP) (TMP) synthetic conventional polyurethanes.People attempt to add antibiotic composition in the conventional polyurethanes material, but its anti-microbial effect time is shorter, less stable.
The objective of the invention is to propose a kind of polyurethane material and preparation method thereof with long stable effect anti-microbial effect.
The antibacterial polyurethane material that the present invention proposes is a kind of with tannin or comprise the polyurethane material that the bark liquefaction thing (being the tannin polyvalent alcohol) of tannin obtains as linking agent.Because the existence of tannin composition makes this polyurethane material have bacteriostatic action.
The synthetic component of the antibacterial polyurethane that the present invention proposes is as follows: tannin polyvalent alcohol A is partly or entirely substituted common polyvalent alcohol B form Pluronic polyols: Ax+B (1-x), 0.1≤x≤1.Pluronic polyols with a unit weight (for example 1000 grams) is a radix, be added with 0.1-0.5% and (refer to the Pluronic polyols amount to be the weight percent of radix, triethylenediamine down together) (brief note is TEDA) catalyzer, 1-5% add the technical pure vulcabond that 30-60% is arranged as the water of whipping agent, the technical pure silicone oil of 1.0-1.3%.Obtain required polyurethane material through reaction.Wherein, technical pure vulcabond flexible foam can use TDI (Chinese is 2,4 one tolylene diisocyanates), and rigid foam can use MID (Chinese is '-diphenylmethane diisocyanate), OH/NCO=0.90-1.24.
Among the present invention, the synthetic component of tannin polyvalent alcohol is as follows: a unit weight with the liquefied reagent prepared by PEG400, a condensed ethandiol (brief note be DEG) and sulfuric acid is a radix, and adding has the tannin of 10-30% or comprises the bark of tannin.Obtain required tannin polyvalent alcohol through reaction.Its hydroxyl is 4.12-7.10mmolKOH/g, and acid number is 0.15-0.17mmol KOH/g.The component proportioning of above-mentioned liquefied reagent is: with sulfuric acid is 1 unit weight, and then DEG is 4.5-5.5, and PGE400 is 90-100.
The preparation method of the polyurethane material that the present invention proposes is as follows: with the Pluronic polyols of a unit weight (for example 1000 grams): Ax+B (1-x), (wherein A is the tannin polyvalent alcohol 0.1≤x≤1 is for radix, B is common polyvalent alcohol), the TEDA catalyzer that adds 0.1-0.5% successively, 1-5% is as the water of whipping agent, the technical pure silicone oil of 1.0-1.3%, fully mix, the technical pure vulcabond that in high-speed stirring, adds 30-60% then, high-speed stirring 10-30 injects after second through in the mould of preheating, under 50-80 ℃ of temperature, solidify, promptly get polyurethane material with anti-microbial effect.
Among the present invention, the preparation method of described tannin polyvalent alcohol is as follows: prepare liquefied reagent by PEG400, glycerine and sulfuric acid by aforementioned proportioning.Under nitrogen protection and mechanical stirring, liquefied reagent is heated to 140-170 ℃, add liquefied reagent weight 10-30% tannin or comprise the bark of tannin, react 100-140 minute, cool off.Excessive sulfuric acid neutralizes with the NaOH aqueous solution (45-55wt%), promptly gets the tannin polyvalent alcohol.Its hydroxyl value and acid number see before and state.
The anti-microbial property of polyurethane material of the present invention is tested and is estimated as follows:
1, for the examination bacterial classification
Streptococcus aureus ATCC 25923, intestinal bacteria ATCC 25922, Pseudomonas aeruginosa ATCC 27853, salmonella typhi ATCC 25923, dysentery bacterium ATCC 12022, false unit cell Pseudomonas aeruginosa ATCC27853, Bacillus proteus ATCC 13315, wax-shaped bacillus clinical separation strain-1, Staphylococcus albus, clinical separation strain-1, Salmonella bacillus typhi murium ATCC 14028, flavacin 1.30.
Above bacterial classification is provided by Shanghai City food supervision and inspection institute and microorganism teaching and research room of Shanghai Second Emdical University.
2, bacteriostatic test
With reference to the in-vitro antibacterial drug sensitivity test, adopt tube dilution method and agar diffusion method to measure minimum inhibitory concentration and antibacterial circle diameter size.
(1) mensuration of minimum inhibitory concentration MIC: tube dilution method
Get tannin stoste, use MH (caseinhydrolysate) broth culture respectively, be diluted to some concentration, respectively get 1ml, mix mutually with various bacteria suspension 0.1ml respectively, fully mixing with double dilution method.37 ℃ of various microbial culture, 24h takes out.Adopt the method for plate culture count, and do blank test with coordinative solvent simultaneously.
Get 0.1ml and be seeded on the plate, after 37 ℃ of 24h cultivate, take out and observe bacterial count, the aseptic long negative pipe of being born is found out the minimum inhibitory concentration pipe, then is the minimum inhibitory concentration of tannin liquid to this bacterium.
(2) mensuration of antibacterial circle diameter size (agar diffusion paper disk method)
Supply to try the bacterium bacterial classifications respectively with its suitable solid slant culture base various in advance, carry out the strain inclined plane activation respectively.Various then bacterial classifications are pickings two ring lawns respectively, and each is made with sterilized water and contains the bacterium number and be about 10
6The bacteria suspension of CFU/ml, stand-by.
Being poured on respectively on two dish plates after the various yeast culture bases thawings of above preparation, after the cooled and solidified, dip in respectively with aseptic cotton carrier and to get various bacteria suspensions, spread upon the suitable substratum plate of various bacterium surface equably, put in 37 ℃ of incubators and take out behind the 15min, purpose makes the agar surface drying, and is stand-by.
Select the special-purpose drug sensitive test paper of diameter 6.35mm, water regain 20ml, make every to contain with adding quadrat method piecewise for test agent 50 μ g, be attached to above-mentioned various containing on the bacterium plate, various for certain 4 (result asks its mean value) of distance subsides in test agent scraps of paper interval in every plate.Then each plate is put into the suitable temperature incubation chamber of various bacterium and cultivated (37 ℃ on bacterium is cultivated 24h).Simultaneously do blank test with corresponding solvent.Measure the size of its antibacterial circle diameter after the taking-up respectively.
(3) moist chamber hanging slice method
Tested sample WT-PU is tailored into 2 * 2cm size with TMP-PU, be suspended in the airtight container of energy, evenly spray 10
6-10
7Individual/ml Aspergillus flavus suspension liquid, move to and cultivate (28 ℃ of temperature, relative humidity 98%) in the temperature and humidity regulator, regularly observations and record write down 7 days, 14 days, 21 days, 28 days altogether.The result measures: specimen surface does not have the mycelia growth, and mildew-resistant power is assessed as 0 grade, and the mycelial growth area is no more than gross area 1/3rd, 1 grade of mildew-resistant power evaluation.The mycelial growth area surpasses gross area 1/3rd and is no more than 2/3rds, 2 grades of mildew-resistant power evaluations.The mycelial growth area surpasses gross area 2/3rds, 3 grades of mildew-resistant power evaluations.Generally through after the test of 28 days fixed temperature and humidity spray bacterium, material mildew-resistant power reaches 0 or 1 grade for qualified.
3, result
Table 1 tube dilution method minimum inhibitory concentration (MIC)
Minimum inhibitory concentration (MIC)
Tannin mg/ml staphylococcus aureus 0.625 Escherichia coli 2.5 Pseudomonas aeruginosas 1.25 salmonella typhis 1.25 are to Hayes shigella dysenteriae 2.5 proteus 0.625 wax-shaped bacillus 1.25 staphylococcus albus 0.625 Salmonella bacillus typhi murium 2.5
* data are secondary revision test mean value in the table
Tannin is summarized in table 1 to the minimum inhibitory concentration of various bacterial classifications, and the result shows that tannin all has bacteriostatic action preferably to above bacterial classification.
The various samples of table 2 are to supplying examination bacterium antibacterial circle diameter (mm)
For examination bacterial classification tannin WT-PU TMP-PU staphylococcus aureus 11 13-Escherichia coli 8 9-Pseudomonas aeruginosa 8 9-salmonella typhi 9 10-to Hayes dysentery bacillus 8 9-proteus 10 9-wax-shaped bacillus 11 11-staphylococcus albus 12 11-Salmonella bacillus typhi murium 9 9-
Result shown in the table 2 shows that tannin has bacteriostatic action, more meaningfully be that raw material synthetic tannin urethane (WT-PU) can keep various biocidal properties for the examination bacterium with the tannin, particularly the inhibition effect to streptococcus aureus, Staphylococcus albus is comparatively remarkable.And to be used as the TriMethylolPropane(TMP) (TMP) of polyurethane cross-linking agent usually, the synthetic conventional polyurethanes that uses the same method (TMP-PU) does not all have anti-microbial effect for the examination bacterial classification to each.
The experimental result of greenhouse hanging slice method shows, after cultivating in 28 days, and the last no mould-growth of WT-PU, mildew-resistant power is assessed as 0 grade, and antimycotic ability is promptly arranged, and a small amount of mould-growth is only arranged on the contrast TMP-PU, the mycelial growth area is less than 1/3rd, and mildew-resistant power is assessed as 1 grade.
The general property that had both possessed conventional polyester with the urethane of tannin preparation, has above-mentioned anti-microbial property again, tannin is present in the molecular structure of urethane as the linking agent of urethane, therefore compares with the antibiotic composition of adding in the common material, and the anti-microbial property of tannin urethane keeps long stable effect.And this material can be degraded under the effect of soil microorganisms, can avoid the pollution of common polyurethane material waste to environment.This polyurethane material field that is widely used.For example: can be used for making plant material urethane wrapping material one time, polyurethane sole materials, elasticity toy, furniture sofa and medical device etc.
Embodiment 1:
Synthetic component: the polyethers propylene oxide adopts N330:50g, TDI:20g, diethanolamine: 0.25g, tin catalyst: 0.16g, water: 0.2ml (containing the 7.5%TEDA catalyzer), silicone oil: 1g, tannin: 15g.Prepare the tannin polyvalent alcohol by preceding method, and further prepare antibacterial polyurethane material.Its performance index are:
Rebound degree: 54%,
Density: 55Kg/m
3,
Compressive strength: 7.4Kpa (25%), 9.0Kpa (45%), 38.4Kpa (65%),
For examination bacterium antibacterial circle diameter (mm): 9-13, mildew-resistant power evaluation: 0 grade.
This material can be in order to make automobile-used cushion and sofa etc.
Embodiment 2:
Synthetic component: polyester (oxalic acid ester): 50g, MDI:20g, tin catalyst: 1.3g, water: 0.1ml (containing the 7.5%TEDAization agent), silicone oil: 1.4g, tannin: 10g.Prepare the tannin polyvalent alcohol by preceding method, and further prepare antibacterial polyurethane material, its performance index are:
Density: 450-750Kg/m
3,
Hardness (Shao Shi): 55-90A,
Tensile strength: 6-8.5Mpa, tear strength 25-40N/mm,
For examination bacterium antibacterial circle diameter (mm): 9-12,
The evaluation of mildew-resistant power: 0 grade,
This material can be in order to make material for sole of shoe.
Embodiment 3:
Synthetic component: plant polyatomic alcohol: 50g, MDI:68g, tin catalyst: 0.45g, water: 2.0ml, the TEDAization agent: 0.35, silicone oil: 0.5g, tannin: 11g.Connect preceding method and prepare the tannin polyvalent alcohol, and further prepare antibacterial polyurethane material, its performance index are:
Density: 20Kg/m
3,
Compressive strength: 12Kpa,
Young's modulus: 134Kpa,
For examination bacterium antibacterial circle diameter (mm): 9-12,
Mildew-resistant power evaluation: 0 grade.
This material can be in order to make the low density wrapping material.
Claims (5)
1, a kind of antibacterial polyurethane material is characterized in that with tannin or the liquefaction thing of bark that comprises tannin as its linking agent.
2, antibacterial polyurethane material according to claim 1, it is characterized in that synthetic component is as follows: with the Pluronic polyols of forming by tannin polyvalent alcohol A and common polyvalent alcohol B of a unit weight: Ax+B (1-x), 0.1≤x≤1 is a radix, add TEDA catalyzer that 0.1-0.5% is arranged, 1-5% as the water of whipping agent, the technical pure silicone oil of 1.0-1.3%, add the technical pure vulcabond that 30-60% is arranged, obtain through reaction.
3, antibacterial polyurethane material according to claim 1 and 2, the synthetic component that it is characterized in that the tannin polyvalent alcohol is as follows: the liquefied reagent by PEG400, a condensed ethandiol and sulfuric acid preparation with a unit weight is a radix, add the tannin that the tannin of 10-30% is arranged or contain bark, make through reaction; The component proportioning of liquefied reagent is: with sulfuric acid is 1 unit weight, and then a condensed ethandiol is 4.5-5.5, and PGE400 is 90-100.
4, a kind of preparation method of antibacterial polyurethane material, it is characterized in that the Pluronic polyols of forming by tannin polyvalent alcohol A and common polyvalent alcohol B with a unit weight: Ax+B (1-x), 0.1≤x≤1 is a radix, the TEDA catalyzer, 1-5% that add 0.1-0.5% successively fully mix as the water of whipping agent, the technical pure silicone oil of 1.0-1.3%; The technical pure vulcabond that in high-speed stirring, adds 30-60% then; High-speed stirring 10-30 injects after second through in the mould of preheating, solidifies under 50-80 ℃ of temperature.
5, the preparation method of antibacterial polyurethane material according to claim 4; it is characterized in that under the preparation process of said tannin polyvalent alcohol: with sulfuric acid is 1 unit weight; then get DEG4.5-5.5; getting PEG400 is 90-100; the liquefied reagent of under nitrogen protection and mechanical stirring the three being formed is heated to 140-170 ℃; add liquefied reagent weight 10-30% tannin or comprise the bark of tannin, react 100-140 minute, cool off.
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CN 01113420 CN1128185C (en) | 2001-06-12 | 2001-06-12 | Antibacterial polyurethane material and its prepn. |
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Cited By (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN102675581A (en) * | 2012-03-12 | 2012-09-19 | 北华大学 | Method for preparing biodegradable polyurethane foam by liquefied modification of bark powder and lignin |
CN105778075A (en) * | 2016-03-15 | 2016-07-20 | 长春工业大学 | Tannin-grafted biodegradable polyester |
CN107602800A (en) * | 2017-09-29 | 2018-01-19 | 鹤山市杰之星五金实业有限公司 | A kind of soft bubble of environment-protecting polyurethane and preparation method thereof |
CN112079981A (en) * | 2020-09-21 | 2020-12-15 | 北京化工大学 | Polyurethane foam material |
CN112888336A (en) * | 2018-11-19 | 2021-06-01 | 株式会社爱世克私 | Sole member, shoe, and method for manufacturing sole member |
CN115612441A (en) * | 2022-12-15 | 2023-01-17 | 山东一诺威聚氨酯股份有限公司 | Environment-friendly bacteriostatic adhesive for wood boards and preparation method and application thereof |
-
2001
- 2001-06-12 CN CN 01113420 patent/CN1128185C/en not_active Expired - Fee Related
Cited By (10)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN102675581A (en) * | 2012-03-12 | 2012-09-19 | 北华大学 | Method for preparing biodegradable polyurethane foam by liquefied modification of bark powder and lignin |
CN102675581B (en) * | 2012-03-12 | 2016-08-10 | 北华大学 | The method that biodegradable polyurethane foam is prepared in bark powder, liquefying lignin modification |
CN105778075A (en) * | 2016-03-15 | 2016-07-20 | 长春工业大学 | Tannin-grafted biodegradable polyester |
CN105778075B (en) * | 2016-03-15 | 2018-07-10 | 长春工业大学 | A kind of tannin is grafted biodegradable polyesters |
CN107602800A (en) * | 2017-09-29 | 2018-01-19 | 鹤山市杰之星五金实业有限公司 | A kind of soft bubble of environment-protecting polyurethane and preparation method thereof |
CN112888336A (en) * | 2018-11-19 | 2021-06-01 | 株式会社爱世克私 | Sole member, shoe, and method for manufacturing sole member |
CN112888336B (en) * | 2018-11-19 | 2022-07-26 | 株式会社爱世克私 | Sole member, shoe, and method for manufacturing sole member |
US11517075B2 (en) | 2018-11-19 | 2022-12-06 | Asics Corporation | Shoe sole member, shoe, and method for manufacturing shoe sole member |
CN112079981A (en) * | 2020-09-21 | 2020-12-15 | 北京化工大学 | Polyurethane foam material |
CN115612441A (en) * | 2022-12-15 | 2023-01-17 | 山东一诺威聚氨酯股份有限公司 | Environment-friendly bacteriostatic adhesive for wood boards and preparation method and application thereof |
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CN1128185C (en) | 2003-11-19 |
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