CN1374364A - Prepn of curing allochroic film - Google Patents
Prepn of curing allochroic film Download PDFInfo
- Publication number
- CN1374364A CN1374364A CN 02114966 CN02114966A CN1374364A CN 1374364 A CN1374364 A CN 1374364A CN 02114966 CN02114966 CN 02114966 CN 02114966 A CN02114966 A CN 02114966A CN 1374364 A CN1374364 A CN 1374364A
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- China
- Prior art keywords
- film
- shearing
- curing
- allochroic
- method described
- Prior art date
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- 238000010008 shearing Methods 0.000 claims abstract description 31
- 229920002678 cellulose Polymers 0.000 claims abstract description 29
- 239000001913 cellulose Substances 0.000 claims abstract description 29
- 239000007788 liquid Substances 0.000 claims abstract description 12
- 238000000034 method Methods 0.000 claims abstract description 12
- 239000000178 monomer Substances 0.000 claims abstract description 12
- 239000004973 liquid crystal related substance Substances 0.000 claims abstract description 10
- 239000000463 material Substances 0.000 claims abstract description 6
- NIXOWILDQLNWCW-UHFFFAOYSA-N Acrylic acid Chemical compound OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 claims description 13
- -1 ethyl-cyanoethyl Chemical group 0.000 claims description 10
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 claims description 10
- 229920002554 vinyl polymer Polymers 0.000 claims description 10
- 238000002360 preparation method Methods 0.000 claims description 8
- HVYWMOMLDIMFJA-DPAQBDIFSA-N cholesterol group Chemical group [C@@H]1(CC[C@H]2[C@@H]3CC=C4C[C@@H](O)CC[C@]4(C)[C@H]3CC[C@]12C)[C@H](C)CCCC(C)C HVYWMOMLDIMFJA-DPAQBDIFSA-N 0.000 claims description 6
- 239000003999 initiator Substances 0.000 claims description 5
- 239000001856 Ethyl cellulose Substances 0.000 claims description 4
- ZZSNKZQZMQGXPY-UHFFFAOYSA-N Ethyl cellulose Chemical group CCOCC1OC(OC)C(OCC)C(OCC)C1OC1C(O)C(O)C(OC)C(CO)O1 ZZSNKZQZMQGXPY-UHFFFAOYSA-N 0.000 claims description 4
- 229920001249 ethyl cellulose Polymers 0.000 claims description 4
- 235000019325 ethyl cellulose Nutrition 0.000 claims description 4
- RWCCWEUUXYIKHB-UHFFFAOYSA-N benzophenone Chemical compound C=1C=CC=CC=1C(=O)C1=CC=CC=C1 RWCCWEUUXYIKHB-UHFFFAOYSA-N 0.000 claims description 3
- 239000012965 benzophenone Substances 0.000 claims description 3
- 230000002535 lyotropic effect Effects 0.000 claims description 3
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 claims description 2
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 claims description 2
- 125000003011 styrenyl group Chemical group [H]\C(*)=C(/[H])C1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 claims description 2
- 238000006116 polymerization reaction Methods 0.000 abstract description 5
- 150000001336 alkenes Chemical class 0.000 abstract 1
- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 abstract 1
- 230000015572 biosynthetic process Effects 0.000 description 5
- 239000004986 Cholesteric liquid crystals (ChLC) Substances 0.000 description 4
- 239000003086 colorant Substances 0.000 description 4
- KMNCBSZOIQAUFX-UHFFFAOYSA-N 2-ethoxy-1,2-diphenylethanone Chemical compound C=1C=CC=CC=1C(OCC)C(=O)C1=CC=CC=C1 KMNCBSZOIQAUFX-UHFFFAOYSA-N 0.000 description 3
- 229920002125 Sokalan® Polymers 0.000 description 3
- 239000002131 composite material Substances 0.000 description 3
- 230000001276 controlling effect Effects 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 239000005357 flat glass Substances 0.000 description 3
- 230000003287 optical effect Effects 0.000 description 3
- 239000004584 polyacrylic acid Substances 0.000 description 3
- 238000003860 storage Methods 0.000 description 3
- 238000004519 manufacturing process Methods 0.000 description 2
- 238000011084 recovery Methods 0.000 description 2
- 230000001105 regulatory effect Effects 0.000 description 2
- 239000007787 solid Substances 0.000 description 2
- 238000000870 ultraviolet spectroscopy Methods 0.000 description 2
- AFPHTEQTJZKQAQ-UHFFFAOYSA-N 3-nitrobenzoic acid Chemical compound OC(=O)C1=CC=CC([N+]([O-])=O)=C1 AFPHTEQTJZKQAQ-UHFFFAOYSA-N 0.000 description 1
- 238000005452 bending Methods 0.000 description 1
- 230000006378 damage Effects 0.000 description 1
- 239000012467 final product Substances 0.000 description 1
- 239000012528 membrane Substances 0.000 description 1
- 150000002828 nitro derivatives Chemical class 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 238000001338 self-assembly Methods 0.000 description 1
- 239000012780 transparent material Substances 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
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- Manufacture Of Macromolecular Shaped Articles (AREA)
- Polarising Elements (AREA)
- Polymerisation Methods In General (AREA)
Abstract
The curing allochroic film is prepared through mixing cellulose derivative and olefin monomer to form cholest type liquid crystal solution, adding photoinitiator to form liquid film, shearing liquid film, letting stand for 1 sec to 6 hr and light polymerization under UV light for 2-5 min to obtain curing allochroic material with cholest phase structure maintained. Of the process, the shearing is controlled to have a shearing strength of 1-1000 Pa and shearing rate of 0.01-100 mm/s. The said process can increase factor to regulate the color of the curing allochroic film and thus regulate the color of the film for practical need.
Description
Technical field
The present invention relates to a kind of preparation method of curing allochroic film, especially have the preparation method of the curing allochroic film of cholester structure.
Technical background
Curing allochroic film with cholester structure had both had the peculiar optical property of cholesteryl liquid crystal, under certain condition owing to the performance with selective reflection visible light demonstrates bright colour, color can change with the difference of viewing angle, and it has stability preferably again.All the time, this research, development and application with curing allochroic film of cholester structure gets more and more people's extensive concerning.The method for preparing this class colour film has a lot, Chinese patent ZL 97114236.X (notification number CN 1060504C, day for announcing 2001.1.10) a kind of solid composite colour film is disclosed, its preparation method is to adopt derivatived cellulose and vinyl monomer the two mixes the molten type liquid crystal that causes of formation by 30～65wt%, add M-nitro benzoic acid and derivative thereof or benzophenone and make light trigger, consumption is 0.5～5% of a monomer weight; The solution pressurization for preparing is formed liquid film, and the controlled polymerization temperature is not higher than 35 ℃, and polymerization time is no more than 20 minutes, and after uviolizing, polymerization obtains solid composite colour film fully.The color of this film determines jointly by the selective reflection optical property of its body color and its cholester structure, and it does not add pigment and the light of a certain wavelength of selective reflection presents different color with the viewing angle difference, has the special optical effect.The color of the light of its body color and reflection depends primarily on the content of derivatived cellulose in this film.Mainly also be that content by derivatived cellulose in the controlling diaphragm prepares the curing allochroic film that reflects different colours in preparation process.Photopolymerization temperature in addition also has certain influence to the color of curing allochroic film.
Summary of the invention
The preparation method who the purpose of this invention is to provide a kind of curing allochroic film, it can increase the factor of regulating the curing allochroic film color, regulates the color of film more effectively, adapts to the needs of practical application.
The preparation method of curing allochroic film provided by the invention, be derivatived cellulose to be mixed with vinyl monomer to form lyotropic cholesteryl liquid crystal solution earlier, add light trigger, make liquid film evenly, this liquid film is applied shearing action, leave standstill then, the time that light gathered 2～5 minutes under UV-light obtains remaining with the curing allochroic material of cholester structure again.
Wherein the shearing action may command shearing resistance that solution is applied is at 1～1000Pa, and speed is in 0.01～100mm/s (mm/second), especially can be shearing resistance at 10～500Pa, speed is at 1～10mm/s.
Time of repose after the shearing generally was controlled at 1 second～6 hours, preferred 10 seconds～1 hour.
Wherein derivatived cellulose is selected from ethyl cellulose, ethyl cellulose acetate, ethyl-cyanoethyl cellulose etc., and vinyl monomer is selected from vinylbenzene, vinylformic acid, acrylate etc., and the proportioning of derivatived cellulose and vinyl monomer is generally 30～60wt%.
Light trigger is generally st-yrax and derivative or benzophenone initiator, is 0.5～5wt% of vinyl monomer weight.
The present invention is mixing derivatived cellulose formation lyotropic cholesteryl liquid crystal solution with vinyl monomer, add light trigger, evenly the back pressurization forms liquid film, and this liquid film is applied shearing action, because liquid crystal molecule is subject to the ambient conditions influence, produces different arrangement modes.Cholester structure can be influenced by extraneous shearing action and changes in the derivatived cellulose cholesteric liquid crystal solution, and the body color changeableization of corresponding cured film is to colourless.This just provides a kind of strong effective ways of controlling the cured film color.After cholester structure was sheared effect orientation destruction in the cholesteric liquid crystal, liquid crystal molecule was orientated along the shearing force direction, and liquid crystal solution loses original reflected light performance and is water white transparency.But because the cholesteric liquid crystal molecule is a chirality, they can carry out self-assembly, arrange by former cholester structure again.By certain relaxation time, former cholester structure can recover voluntarily, also recovers simultaneously catoptrical performance, the recovery of getting back of its body color.The intensity of controlling shear effect, speed and relaxation time can effectively be regulated the color of this variable color film.
The condition size that in the method provided by the invention the curing allochroic film color is exerted an influence is followed successively by: the intensity and the speed of derivatived cellulose content＞shearing back storage period＞shearing.And the thickness of material can change catoptrical intensity.
Table 1: different derivatived cellulose content are to the influence (is example with ethyl-cyanoethyl cellulose/vinylformic acid) of membrane body color
Table 2: finite concentration variable color film, in the colour-change (reducing) of different viewing angles
| Mierocrystalline cellulose/vinylformic acid | ??43∶57 | ?46∶54 | ??48∶52 | ?52∶48 |
| Wavelength value (nm) | ????742 | ??626 | ????571 | ???425 |
| Color | Red | Orange red | Yellowish green | Blue |
| The viewing angle value (°) | ??90 | ???80 | ???70 | ???60 |
| The wavelength change rate of color (is the body value with 90 ° colors) | ???1 | ??0.98 | ??0.93 | ??0.87 |
Table 3: the body colour-change of Mierocrystalline cellulose cholesteric liquid crystal solution under shearing action (in intensity be under the shearing action of 200pa, speed 3mm/S situation be example) with ethyl-cyanoethyl cellulose/vinylformic acid cholesteryl phase solution
| Mierocrystalline cellulose/vinylformic acid is than (52: 48) | Mierocrystalline cellulose/vinylformic acid is than (49: 51) | ||
| Storage period (branch) after shearing | Wavelength value (nm) | Storage period (branch) after shearing | Wavelength value (nm) |
| ?????????0 | Colourless | ?????????0 | Colourless |
| ?????????1 | ?????397 | ?????????1.5 | ?????507 |
| ?????????2 | ?????440 | ?????????3 | ?????554 |
| ????????10 | ?????462 | ?????????10 | ?????575 |
| ????????30 | ?????468 | ?????????30 | ?????578 |
The recovery of shearing back cholesteryl phase solution body color is exponential form, and promptly preceding fast back is slow.Big shearing resistance and fast shearing rate will make body change in color scope strengthen, and it is also slow that cholesteryl phase recovers, and promptly the time of placement is identical after the effect, and the wavelength of the liquid crystal solution that shearing resistance is big or shearing rate is fast is smaller.
The invention has the advantages that the condition that can control production process flexibly, obtain the curing allochroic film of different colours, production method is implemented simple, and is reliable, can change one of influence condition according to different situations during practical application and get final product.Material feedstock adopts derivatived cellulose, and the source is abundant, with low cost.The composite colour mould material is a transparent material, and certain snappiness is arranged, bending that can be suitable, thus better processability and applicability are arranged.
Embodiment
Embodiment 1
Ethyl-cyanoethyl cellulose and vinylformic acid were mixed by 43: 57 and 49: 51 respectively, add Benzoin ethyl ether (vinylformic acid weight 2%) as initiator.Two kinds of solution are clipped in the thick liquid film of formation 80 μ m between two sheet glass, after the shearing action of 100Pa, speed 10mm/s, place respectively after 10 minutes and after 2 minutes, obtain the body color respectively and be red and blue ethyl-cyanoethyl cellulose/polyacrylic acid laminated film with the 250W ultraviolet source irradiation.
Embodiment 2
Ethyl-cyanoethyl cellulose and vinylformic acid were mixed by 49: 51, add Benzoin ethyl ether (vinylformic acid weight 2%) as initiator.This solution is clipped in the thick liquid film of formation 80 μ m between two sheet glass, after the shearing action of 200Pa, speed 3mm/s, placed respectively 1 minute, use the 250W ultraviolet source irradiation after 2 minutes after 10 minutes and 1 hour, obtaining the body color respectively is purple and blue ethyl-cyanoethyl cellulose/polyacrylic acid laminated film.Measure through ultraviolet-visible spectrophotometer, 1 minute and 10 minutes colors differ 65nm, and 1 minute and 1 hour color differ 81nm.
Embodiment 3
Ethyl-cyanoethyl cellulose and vinylformic acid were mixed by 52: 48, add Benzoin ethyl ether (vinylformic acid weight 2%) as initiator.This solution is clipped in the thick liquid film of formation 80 μ m between two sheet glass, at difference 200Pa and 800Pa, behind the shear action of speed 5mm/s, place respectively and use the 250W ultraviolet source irradiation after 2 minutes after 3 minutes, acroleic acid polymerization, obtaining the body color is the interior ethyl-cyanoethyl cellulose/polyacrylic acid laminated film of blue light scope.Measure through ultraviolet-visible spectrophotometer, the latter is than the former little 20nm of reflected light wavelength.。
Claims (9)
1, a kind of preparation method of curing allochroic film, be derivatived cellulose to be mixed with vinyl monomer to form lyotropic cholesteryl liquid crystal solution earlier, add light trigger, make liquid film evenly, it is characterized in that this liquid film is applied shearing action, leave standstill then, the time that light gathered 2～5 minutes under UV-light obtains remaining with the curing allochroic material of cholester structure again.
2, according to the method described in the claim 1, the shearing resistance that it is characterized in that described shearing action is 1～1000Pa, and speed is 0.01～100mm/s.
3,, it is characterized in that described shearing resistance is 10～500Pa according to the method described in the claim 2.
4,, it is characterized in that described speed is 1～10mm/s according to the method described in the claim 2.
5,, it is characterized in that the time of repose after the described shearing is 1 second～6 hours according to the method described in claim 1 or 2.
6,, it is characterized in that the time of repose after the described shearing is 10 seconds～1 hour according to the method described in the claim 5.
7, according to the method described in the claim 1, it is characterized in that described derivatived cellulose is selected from ethyl cellulose, ethyl cellulose acetate, ethyl-cyanoethyl cellulose, vinyl monomer is selected from vinylbenzene, vinylformic acid, acrylate.
8, according to the method described in the claim 1, the proportioning that it is characterized in that described derivatived cellulose and vinyl monomer is 30～60wt%.
9,, it is characterized in that described light trigger is st-yrax and derivative or benzophenone initiator, is 0.5～5wt% of vinyl monomer weight according to the method described in the claim 1.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CNB021149666A CN1166748C (en) | 2002-03-15 | 2002-03-15 | Prepn of curing allochroic film |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CNB021149666A CN1166748C (en) | 2002-03-15 | 2002-03-15 | Prepn of curing allochroic film |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| CN1374364A true CN1374364A (en) | 2002-10-16 |
| CN1166748C CN1166748C (en) | 2004-09-15 |
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| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CNB021149666A Expired - Fee Related CN1166748C (en) | 2002-03-15 | 2002-03-15 | Prepn of curing allochroic film |
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| Country | Link |
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| CN (1) | CN1166748C (en) |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| KR100816141B1 (en) | 2003-03-31 | 2008-03-24 | 샤프 가부시키가이샤 | Liquid crystal display device and fabrication method thereof |
| CN101833122A (en) * | 2010-03-22 | 2010-09-15 | 袁敏华 | Color-changing optical protection layer |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN101417564B (en) * | 2008-10-23 | 2011-02-02 | 上海复旦天臣新技术有限公司 | Anti-counterfeiting film with double color-changing pattern and preparation method thereof |
-
2002
- 2002-03-15 CN CNB021149666A patent/CN1166748C/en not_active Expired - Fee Related
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| KR100816141B1 (en) | 2003-03-31 | 2008-03-24 | 샤프 가부시키가이샤 | Liquid crystal display device and fabrication method thereof |
| CN101833122A (en) * | 2010-03-22 | 2010-09-15 | 袁敏华 | Color-changing optical protection layer |
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| Publication number | Publication date |
|---|---|
| CN1166748C (en) | 2004-09-15 |
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